Académique Documents
Professionnel Documents
Culture Documents
prepared for
by
in conjunction with
SIGURDSON & ASSOCIATES
MARCH 2000
TABLE OF CONTENTS
PAGE
DISCLAIMER...............................................................................................................................................................................viii
-i-
TABLE OF CONTENTS
PAGE
5.5.3 Production Technology for Propylene Oxide (PO) and Glycol ....................................................... 37
5.5.4 Technical Business Trends in Propylene Oxide (PO) and Glycol ................................................... 40
5.5.5 Potential for Alberta with Propylene Oxide (PO) and Glycol ......................................................... 40
5.6 Propylene Ethers ............................................................................................................................................. 40
5.6.1 North American Market for Propylene Ethers................................................................................. 41
5.6.2 Major Producers of Propylene Ethers.............................................................................................. 41
5.6.3 Production Technology for Propylene Glycol Ethers ...................................................................... 41
5.6.4 Technical Business Trends in Propylene Glycol Ethers .................................................................. 42
5.6.5 Potential for Alberta with Propylene Glycol Ethers ........................................................................ 42
5.7 n-Butanol......................................................................................................................................................... 42
5.7.1 North American Market for n-Butanol ............................................................................................ 42
5.7.2 Major Producers of n-Butanol ......................................................................................................... 42
5.7.3 Production Technology for B-butanol ............................................................................................. 43
5.7.4 Technical Business Trends in n-Butanol ......................................................................................... 44
5.7.5 Potential for Alberta for n-Butanol.................................................................................................. 44
5.8 Acrylic Acid (AA)........................................................................................................................................... 44
5.8.1 North American Market for Acrylic Acid (AA) .............................................................................. 44
5.8.2 Major Producers of Acrylic Acid (AA) ........................................................................................... 45
5.8.3 Production Technology for Acrylic Acid (AA) ............................................................................... 45
5.8.4 Technical Business Trends in Acrylic Acid (AA) ........................................................................... 46
5.8.5 Potential in Alberta for Acrylic Acid (AA) ..................................................................................... 46
5.9 Isopropanol/Acetone ....................................................................................................................................... 46
5.9.1 North American Market for Isopropanol/Acetone........................................................................... 46
5.9.2 Major Producers of Isopropanol/Acetone........................................................................................ 47
5.9.3 Isopropanol Production ................................................................................................................... 47
5.9.4 Technical Business Trends in Isopropanol/Acetone........................................................................ 48
5.9.5 Potential for Alberta with Isopropanol/Acetone .............................................................................. 48
5.10 2-Ethyl Hexanol .............................................................................................................................................. 49
5.10.1 North American Market for 2-Ethyl Hexanol.................................................................................. 49
5.10.2 Major Producers of 2-Ethyl Hexanol............................................................................................... 49
5.10.3 Production Technology for 2-Ethyl Hexanol................................................................................... 49
5.10.4 Technical Business Trends in 2-Ethyl Hexanol............................................................................... 50
5.10.5 Potential for Alberta for 2-Ethyl Hexanol ....................................................................................... 50
5.11 Atactic Polypropylene (APP) .......................................................................................................................... 50
5.11.1 Production of Atactic Olefins .......................................................................................................... 50
5.11.2 Process Technology......................................................................................................................... 51
5.11.3 Markets and Outlook ....................................................................................................................... 51
5.11.4 Investment Potential ........................................................................................................................ 52
5.12 Ranking of Propylene Product Potential ......................................................................................................... 52
6.0 THREE PRODUCTS WITH POTENTIAL FOR ALBERTA ........................................................................................ 55
6.1 Chemicals Selected for Further Analysis ........................................................................................................ 55
6.2 Polypropylene (PP) ......................................................................................................................................... 55
6.2.1 Market Potential .............................................................................................................................. 55
6.2.2 Trade in Polypropylene (PP) ........................................................................................................... 56
6.2.3 Technology Shifts in Polypropylene (PP) Resins............................................................................ 57
6.2.4 Cost Competitiveness of Alberta in PP Resins ................................................................................ 58
6.2.5 Alberta Potential for Polypropylene (PP) Resins............................................................................. 59
6.3 Acrylonitrile (ACN) ........................................................................................................................................ 59
6.3.1 Market Potential for ACN ............................................................................................................... 59
6.3.2 Trade in Acrylonitrile (ACN) .......................................................................................................... 60
6.3.3 By Product Potential in Canada....................................................................................................... 61
6.3.4 Technology Shifts in ACN Production............................................................................................ 62
6.3.5 Cost Competitiveness of Alberta for ACN Production.................................................................... 62
6.3.6 Alberta Potential for Acrylonitrile (ACN)....................................................................................... 62
6.4 Acrylic Acid (AA) and Acrylates.................................................................................................................... 63
6.4.1 Acrylic Acid (AA)........................................................................................................................... 63
6.4.2 Market Potential for Acrylic Acid (AA).......................................................................................... 64
- ii -
TABLE OF CONTENTS
PAGE
- iii -
LIST OF TABLES
PAGE
- iv -
LIST OF TABLES
PAGE
-v-
LIST OF FIGURES
PAGE
- vi -
GLOSSARY
- vii -
DISCLAIMER
The contents, conclusions, recommendations and numbers in this report are the sole responsibility of T. J. McCann and
Associates Ltd. and its associated consultants. They may or may not be in agreement with views and/or policies of the Alberta
Department of Economic Development (AED). It is also to be noted that this study – with the sole exception of confirmation of
one data point – has been carried out with no related rapport with TransCanada Midstream (TCMS) who are proceeding on a
byproduct propylene collection and purification system.
- viii -
1.0 EXECUTIVE SUMMARY
INTRODUCTION
TransCanada Midstream (TCMS) is currently putting together a very significant byproduct recovery and purification scheme, but
no announcements have yet appeared of local derivative facilities. This study independently considered propylene supply options
and examined a variety of propylene derivatives to define those that appear to fit best in Alberta. At the same time, key chemical
companies with propylene derivative interests were identified.
SUPPLY
280-ktonnes a year of propylene were conservatively estimated as available from byproduct sources in 2005. As byproduct
sources have some risks, ups, and downs, a prudent chemical company would perhaps discount supply to the order of 200,000-
kty to ‘guarantee’ supply to his facility.
Oil sands upgraders, ethylene plants and refineries are the principal sources with a total production of about 400-kty – some used
now in fuel gas. Some shopped as a concentrate to the U.S. and some connected to gasoline. Each source has a different set of
supply costs and the different source types have wide ranges of impurities. Each source also has more or less need for on-site
facilities to separate propylene-rich streams for central processing. Pipeline and rail receipt is envisaged with a major central
treating and distillation facility to produce polymer grade (PG) propylene with propane and other smaller byproducts from the
raw feed. Major salt cavern storage will be needed to smooth out the plant feed and to insure highly reliable product supply.
Very preliminary estimates tend to indicate such byproduct propylene available at about two cents U.S. per pound under the price
on the U.S. Gulf Coast (USGC) before maximizing synergy with existing facilities (as at TCMS).
A route starting from propane was considered for 350-kty of propylene. However, with current propylene product cost slightly
above USGC prices, it will be attractive only as newer technology and more cost cutting lower capital costs. Such reductions are
considered quite possible over the next 3 to 5 years and the propylene to propane value difference could widen from 1998 levels
(as at present). This option appears to warrant further analysis in a year or two.
Polypropylene (PP)
PP is produced as solid beads and moved in bulk rail cars to a variety of markets, e.g., injection and blow molding, fibers, films,
wire and cable. Demand for PP in several forms, some with ethylene and other comonomers, is growing at 6 to 7% a year world
wide, requiring 350 to 400-kty of added North American capacity each year. Canada currently exports $243 million of PP to the
U.S., but imports $450 (1998 figures). While Asian market growth is most pronounced, there are growing PP markets
worldwide.
Dow is moving into new PP technology/product territories, and its acquisition of Union Carbide adds major more conventional
PP technology depth. Shell Chemical is adding BASF, the world’s largest chemical company, to its Montell PP team – with two
plants already in eastern Canada. There is a long list of other major PP producers not now represented in Alberta.
New catalysts and other technological developments are dramatically broadening the range of grades and of applications.
Acrylonitrile (ACN)
ACN, a liquid product, demand is growing at 6 to 7% a year in Asia as an intermediate for fibers, various resins, and a variety of
chemicals, such as those used in water treatment. North American markets are generally remote from Alberta, but Alberta is
‘close’ to Asian markets via West Coast ports. The propylene and ammonia feedstocks are here at low cost and there are regional
markets, in mining for the byproduct hydrogen cyanide, which is often requires expensive disposal.
It is likely that a series of derivatives would be produced at an AA facility, although AA can be railed/tankered as liquid to
Pacific Rim and to mid continent North American markets.
Dow and Celanese have a new German joint venture producing AA and various derivatives. Celanese, BASF and Union Carbide
(Dow) currently have three of the four North American plants. Degussa-Hüls has a European AA joint venture.
OTHER POSSIBILITIES
Propylene Oxide (PO)
PO and one or more series of derivatives are considered good prospects, but do require isobutane – here now – or more normally
benzene – short in Alberta – feedstocks with very major byproducts – e.g., styrene in the case of benzene as the cofeed. PO
might well have been one of the three short-listed products if the major cofeed/coproduct situation did not exist. Propylene
glycols and various ethers are good PO derivative prospects.
Phenol
Phenol has major regional markets in the production of resins used in various construction board products. Propylene can be a
key feed, along with benzene. An apparent Alberta shortage of benzene must be addressed before phenol production is
considered.
This study was not bullish on isopropanol and acetone, n-butanol, 2-ethyl hexanol (2-EH) and propyl ethers (from isopropanol)
should not be discarded as possible new small-scale Alberta chemical products.
SUMMARY
• Alberta does not have merchant propylene at this time.
• Over 200,000-tonnes a year can be made available from byproduct sources below USGC costs. (TCMS has
already started a collection and purification project.)
• This quantity well fits individual world scale PP, ACN and AA derivative prospects.
• Availabilities of benzene and certain other key chemical intermediates appear to warrant study and promotion, to
extend the list of prospective ‘new’ Alberta chemical products.
• Alberta offers low capital and operating costs and shipping costs to the Pacific Rim are below, those from the
Houston area, although marginally higher to the mid continent area.
• Propylene derivatives should have a strong place in Alberta’s future.
TCMS is building a major propylene byproduct extension to their Redwater natural gas liquids fractionation plant. TCMS is also
constructing facilities at Suncor’s oil sands plant to recover a propylene/propane mix and potentially more or less ethane and
ethylene. The resulting liquid blend will be delivered to the Redwater site via Suncor’s oil sands pipeline and a short local line.
TCMS will be obtaining byproduct propylene from other sources, but no details were available to this study. While this study
essentially overlooks the TCMS propylene program, its very active presence must be considered by all.
Byproduct propylene is available from sites at Joffre, Edmonton (SIA—Strathcona Industrial Association—region), Fort
Saskatchewan/Redwater area (AIH—Alberta’s Industrial Heartland) and the oil sands plants north of Fort McMurray. Due to the
unique availability of salt for storage cavern development, relative central location and proximity to a variety of major chemical
production and natural gas liquids fractionation sites, new propylene processing facilities have been assumed in the AIH.
There are current expansion programs at current oil sands plants and, likely, expansions at regional refineries and an upgrader
that will enhance propylene production through to and perhaps beyond the 2005 period. In addition, the Joffre E3 world’s largest
ethylene unit comes on-stream in 2001. Thus, estimated 2005 byproduct propylene availability is considered as a base, consistent
with project development, permitting, construction, startup of collection and purification facilities, including storage cavern
development, with and propylene derivative facility completion(s).
3.1 Availability
3.1.1 Overall
Table 3.1.1-1 summarizes this study’s estimates of potentially propylene in Alberta and surrounding areas in 2005. The estimates
are by the study team, but confirmed as reasonable by verbal contacts at all but two sources. The table also notes what the team
considers as a ‘likely’ 2005 availability scenario—to be used in later sections of this report as a base case.
The byproduct availability estimates are conservative – they allow for off normal operations, such as shutdowns and related
events, occasional upsets, different catalysts and catalyst conditions (at refineries), new approaches to fouling control in ethylene
furnace tubes, below capacity operation on occasion, and below design process severities on occasion or continuing (at least at
one major source). Two sources provided ranges to cover likely operating severities with mid points used here and another
advised reduced propylene compared to earlier estimates, due to less severe operating conditions. Expansion prospects at three
sources were discussed, but it was too early to assess any increase in propylene availability.
Not all sources will be available, nor will suitable commercial terms be negotiated at all sites. We acknowledge that the ‘likely’
figure is only a judgement call.
The accuracy of the total, is perhaps, at the +20% level with individual accounts less certain. Changing conditions in source units
are to be expected over time and propylene is generally not an economically preferred product at any of the identified sources.
Table 3.1.1-2 notes current and prospective alternate uses for propylene at the various sources, without a capture/purify/chemical
derivative scheme(s). Table 3.1.1-3 provides a brief review of what facilities will be required at various sources for propylene
recovery and transfer. Scheduling of in-plant changes will be very tricky and with major turnarounds only every 2 to 2-1/2 years,
there could well be delayed availabilities from specific various sites. (However, this is roughly the same timing as for large salt
cavern development.)
Alberta EnviroFuels (AEF) currently produce more or less propylene—say 10-kty—depending on the propane content of its
feedstock C4 streams. This propylene now goes to fuel gas. AEF are reported to be considering changing the plant’s processes
and products from methyl tertiary butyl ether (MTBE), but, as yet, without a public decision. Thus, AEF propylene has been
neglected herein. Husky’s Lloydminster Upgrader expansion plans are unknown, hence, no estimate of possible propylene
availability has been made—likely small in the overall picture, in any case.
Note that the Shell Scotford and Parkland Borden refineries produce no propylene.
At the bottom of Table 3.1.1-1 is this study’s judgement of a ‘realistic’ byproduct availability. The 280-kty may appear small,
but prospects perceived to have major challenges economically or major delays to beyond 2005 have been excluded. Only
detailed buyer to supplier negotiations will resolve economically attractive availability from any source. Hopefully, it may prove
possible to attract at least another 100-kty of economic supply than has been assumed in this study.
A prudent propylene consumer is likely to discount the byproduct availability, say, up to 80-kty to assure him of supply at all
times, even if one major source drops out – leaving a ‘recognized’ availability of about 200-kty. Even then, major storage will be
required to assure that rate on a daily basis.
The base case 285-kty of propylene in raw feed streams is an annual average and peaks of 330-kty are likely with minima to
processing at or near 200-kty (using feed cavern storage).
3.2.1 Preamble
There will be byproduct propylene coming from a variety of sources via pipeline and rail, all with differing qualities. Some
trucked material is possible, but not considered in this study.
Once propylene capture facilities are in place, the byproduct processor will be receiving all available feeds, with the possible
partial exception of some from ethylene plant material. Portions of the ethylene plant material could continue to move south, but
only to the extent, that sufficient numbers of railcars continue available. (Reducing such rail fleets appears likely to be important
financial inducements for ethylene plant sources.)
Suncor or Equal
Pipeline(s)
∼ Interface Processing complete
with Distillation
Oil Sands C3
Received in
Batches
C4 or C5 Plus Pipeline to Processing Site
Byproduct
Dow Ethylene Propylene
New Continuous Pipelines Processing
Edmonton Refineries Facility
Bullets
NovaChem Rail
Injection Pumps
2 Wells Minimum
Salt Cavern Storage
• Oil sand material is received in daily or bi-daily batches from the Fort McMurray area.
• The batches are stored at the receipt point and then gradually transferred to the processing facility or to
cavern storage.
• Interfaces (and buffers if used) are segregated and the C3 content distilled off and the bottoms returned
to the main pipeline.
• Local ethylene plant feed will be received by pipeline with Joffre feed by rail. Surface storage will be provided to
allow continuous feed of the ethylene plant blend to processing.
• Edmonton refinery feed will be received by pipeline on a continuous basis and routed directly to processing.
• Other refinery feeds will be received by rail and transferred to surface storage and then to the processing facility
with balancing via the caverns.
• All excess feed will be routed to caverns say two at 500,000 barrels each, to be led to the process as capacity and
product demand permit.
This study has not attempted to optimize the feed/raw propylene storage system. (That will be a very complex study in itself—
e.g., sizing cavern injection pumping will be a major challenge.) The diagram notes a possible cavern withdrawal/filling
Refinery propylene is foreseen as being used here directly for only a few propylene derivatives that were not identified as having
major potential. In addition, even the largest individual propylene-rich streams appear below what is seen here as appropriate to
significant propylene chemical production in Alberta. Any combination of source types will require some processing and/or
distillation for even a refinery product grade. Thus, while smaller-scale opportunities for refinery grade propylene are definitely
to be encouraged, this study has considered only chemical and PG propylene.
Table 3.2.3-1 provides typical propylene product specifications from the literature, but each potential customer will have his own
specifications. In practice, certain parameters in the product will regularly be well under formal specifications and customers will
become used to such qualities. They will in effect become defacto standards.
The primary differences between the two grades are in propane content and trace contaminants (not all shown in the table). The
methylacetylene and propadiene (MAPD) content, is definitely of more concern where PG is standard than when chemical grade
is the normal feed. (Non refinery propylenes and even some refinery propylene may be non-acceptable to ‘refinery’ grade users
due to MAPD content.)
In the byproduct, processing scheme assumed in this study, an option for chemical and PG coproduction is shown. In practice,
there are major differences only in the C3 splitter system between product grades and a PG capability (today using a single tower)
will be a likely decision in any case.
It is important to note that the specifications apply to propylene as delivered to customers—i.e., after caverns, pipelines, railcars,
etc.
C2 – to C3 C4 C3
Fuel Gas Splitter Splitter
Compressor
Hydrogenation Deethanizer (C)
Final
Treater
Purges Final
Chemical To Reflux
Hydro-
Hydrogen Treating Treating
Upgrader
Refinery
Feeds Sulphur
Removal
Hydrogen
(B)
Sulphur
Rich Purge (C)
(D)
Product:
(A) Polymer Grade Propylene to Market
(B) Chemical Grade Propylene to Market (Optional)
(C) Propane to Market
(D) C4+ to Market
Due to its very high MAPD contamination ethylene plant raw feed blend will have a hydrotreater to lower MAPD to 100 or less
ppm (from an inlet design of 50,000-ppm—5%). There will be very appreciable heat generated in this operation and a large cold
recycle will be needed. The MAPD will be converted very largely to propylene, but some hydrogenation to propane may occur,
as well as trace polymerization, perhaps, as far as a thick ‘green’ oil on occasion.
The non-ethylene plant feedstocks require sulphur removal to below 5-ppm. This will be done, probably, via 2 or 3 stages of
processing. Byproduct sources have a habit of bringing unanticipated trace impurities – e.g., phosphorus, antimony, mercury and
nitrogenous compounds. In byproduct processing the chemical treating must consider heavier than propane feedstocks, hence,
the somewhat arbitrary location here ahead of C3 C4 separation. Only allowances for such treating are included here.
The final hydrogenation unit will reduce MAPD to below 10-ppm; distillation in turn will reduce this to near zero in the product
propylene. No significant polymer production is anticipated in this hydrogenation step. Butadiene partial saturation to butylenes
will also occur (improving the quality of the small-scale C4 plus byproduct).
The deethanizer removes all the ethane and lighter components to fuel gas and the C3 C4 splitter produces a C4 plus bottom
product. (There will likely be too much C4 in the original feed to leave in propane. The original feed C4 will have 50 or so
percent olefins, of value to refiners, but requiring hydrogenation if left in for propane, even if it can be.)
The C3 splitter is assumed to be single tower vapour compression reboiled (heat pumped) system (as described further in the later
propane dehydrogenation discussion). Blending a bypass of the final C3 splitter with polygrade product will permit a slightly
lower (utility) cost chemical grade product if desired.
A final guard bed solid adsorbent treater—e.g., for sulphur, CO2, CO, trace metals – has been assumed needed for quality
assurance.
Each source plant will have its own unique value for propylene at any given time prior to any consideration of its separation for
separate processing for sale.
Oil Sands
• Local marginal natural gas supply cost to displace propylene. Note that lower heating value must be used in
calculating the amount of gas required.
• The large amount of co-recovered propane, 2 to 3 times the volume of propylene, must also be replaced.
• As oil sands processing and related cogeneration systems expands, their incremental gas supplies will be coming
from farther and farther south on the TransCanada system unless a new line is built, increasing the cost of such
gas.
• Like all propylene sources oil sand producers will require a premium over fuel or other replacement costs.
Refineries
• Propylene sale from Alberta refineries will reduce alkylate production [C3= + iC4 Æ C7 isomers] and the resulting
loss of very important gasoline blending stock must be made up by:
• Gasoline purchase from others and/or
• Added crude and intermediate processing
• Taking propylene out of alkylation does improve the octane of the remaining (C4) alkylate in-turn this allows
slightly higher yields in the parallel catalytic reforming unit. However, this only makes up for a small portion of
the deficit.
• Extraneous olefinic C4’s may be available to displace the propylene, but this study has not examined such
potential nor its costs.
• Reduced isobutane demand in alkylation appears economically important, reducing overall refining butane
purchases.
• Raw propylene sales from refineries, also reduces related propane sales, but this is not seen as of a great concern.
(Conversely, less isobutane is needed reducing butane purchases.)
• This study has not attempted a valuation of raw refinery propylene, due to very refinery-specific economic bases
beyond an external reviewer’s knowledge.
Note: At the Regina Co-op refinery propylene is polymerized, hence, a different propylene replacement situation exists.
Ethylene Plants
• Here the situation is clearer as the raw propylene now moves to the USGC. Rail transport south is in the order of
3.5 to 4 cents U.S. per pound of propylene and processing costs appear to be in the 6 to 10 cents U.S. per pound
range. However, in some USGC cases, MAPD may be extracted rather than hydrogenated to propylene
complicating valuation.
• Ethylene plant raw propylene value will closely track USGC chemical and polygrade propylene.
B. Capture Costs
As noted in Figure 3.2.4-1, there will be significant facility needs at each oil sands and refinery source. These
facilities will have high utility costs – electricity for compression, especially for low temperature recovery from fuel gas
streams and steam for distillation, particularly at refineries.
Even in the base case, new processing facilities at oil sand and refinery sources are likely to be in the order of $60 to
100 million with operating costs in the $7 to 12 million year range.
C. Transfer Costs
There may be a credit for the major reduction in rail cars now used to transport ethylene plant raw propylene to the USGC,
although some will be needed for other non AIH/SIA source material.
Raw propylene storage facilities will be large as noted above to cope with the widely fluctuating feed streams from other than
local ethylene plant and Edmonton refineries.
Handling and raw feed storage facility costs appear likely to have capital costs in the order of $40 to 50 million for the base case.
(This does not consider a new line from the oil sands area.)
D. Processing Charges
The central facility for the assumed base case could cost in the $60 to 80 million range, but no estimate was attempted in this
study, due to wide range of feeds and process alternates to be considered.
E. Overall Byproduct
The capital costs for the base case scheme appear likely to be in the order of $160 to 230 million, without any credit for rail car
reduction. Possible operation costs have not been totalled due to their high uncertainties.
Review of the preliminary costs indicates the likelihood of PG propylene available at 1 to 2 cents U.S. per pound under the
USGC long-term average price, assuming all grassroots facilities.
It is to be noted that underlying cost factors do not relate directly to USGC propylene values on a short-term basis. There will be
many ups, and downs, with Alberta costs and USGC propylene values not being in sync. Reference (a), for example, has graphs
reflecting very wide swings between USGC propane and propylene with only long-term time averaging of use in estimating
economics.
Propylene shipped to the USGC will receive only the contract or spot USGC value, resulting in roughly a four cents per pound
shipping penalty at the Alberta source. While this study’s prefeasibility level estimates did not show such value for Alberta
byproduct propylene from multiple sources, TCMS and/or other operators may well be able to achieve such pricing for all their
propylene product. To be conservative, this study assumed an Alberta byproduct propylene price of two cents per pound under
USGC prices.
TCMS will be able to achieve significant cost savings compared to a grassroots project, due to co-location with the existing
Redwater natural gas liquids fractionation and salt cavern storage facilities. There appear to be opportunities for integration at
other sites, hence, the above cost estimate could well over estimate the required netback on local propylene sales. As such credits
were not fully assessed, this study has assumed a two cents per pound under USGC price for locally delivered PG propylene.
4.1 Preamble
The ready availability of at least 200-kty appears essential for each of the short-listed chemicals discussed below in Section 6.
This much appears likely to be available from byproduct sources in 2005 with an 80-kty cushion (assuming only 5-tky lost to
propane in the purification system). However, more than one major derivative plant should be targeted and another route to
Alberta merchant propylene should be considered.
Review of the world propylene scene indicates a number of plants now producing propylene from very low-cost propane. While
Alberta does not fall into that category, construction and operating costs (ex utilities) are generally well below these developing
country sites. Thus, Alberta propane to propylene warrants consideration.
Enough propylene for the minimum sized facilities for two of the three short-listed propylene chemicals could be produced in a
current relatively standard single train 350-kty plant. At much above 450-kty we expect a largely two-train design with only
minor scale advantages.
At 350-kty of propylene from propane, approximately 2,150-m3/d (14,000-BPD) of commercial grade propane will be needed.
This compares to Alberta production of 25 to 30,000-m3/d, with over 80% going to export markets. Hence, a 350-kty propylene
from propane facility should have little problem acquiring feedstock via TCMS, Dow, Amoco and/or Chevron AIH storage at
prevailing prices (probably with some summer over purchases and seasonal storage), even with some diversion to the Alliance
pipeline system.
4.2 Technology
Dehydrogenation of propane to propylene via catalytic processes is being practiced in Europe, Saudi Malaysia and Korea. In one
case, a combined propane and isobutane feed is being processed to supply both PP and MTBE feedstocks.1 However, separate
processing at larger-scale is more economic and strongly recommended.
In the combined feed case and most other current propane dehydrogenation facilities, the UOP Oleflex dehydrogenation
technology used is very similar to that used for isobutane to isobutylene at AEF. The catalyst regeneration system at AEF is also
common to that at the propane units and close to that of Shell’s continuous catalytic reformer in the Scotford Refinery.
Other process routes to propane dehydrogenation are practiced in one Antwerp unit and licensed for two new smaller Mid East
units. Due to its predominance and local partial usage, here, we have assumed use of UOP’s Oleflex technology, based on
Reference (a) and discussions with UOP staff (References (b) and (c)). There would be four reactors versus three at AEF and
metallurgy would be higher due to more severe conditions when dehydrogenating propane.
1
Alberta EnviroFuels now dehydrogenate a portion of the propane contaminant in its feed butane, but both unreacted propane and
propylene are routed to fuel gas.
Fuel H2
Gas C3
Fuel Gas Splitter
H2
Purification (C) Compressor
Depropanizer H2
Dehydrogenation Deethanizer
Polymer
Grade
Pipeline Propylene
Hydrogenation Storage
from Pretreatment of MAPD Cavern
NGL Reboiler
Reflux
Frac / Storage
C4 +
Recycle
(C) Propane to Market Propane with traces of C4+
The pretreatment system would reduce sulphur and other contaminants to a very low level to protect the precious metal catalyst
used in dehydrogenation. Essentially, all C4 and any heavier portions of the propane feed and recycle streams would be removed
in the depropanizer. (Note that ethane in the feed carries on through reaction to fuel gas.)
Propane and hydrogen pass through four fired heaters and four moving bed reactors in series as dehydrogenation proceeds to near
the 40% equilibrium level. The reaction products are then processed to remove small quantities of light decomposition
components and hydrogen. A small amount of propadiene/methylacetylene is formed in the reaction and is converted to
propylene in a well-proven low temperature hydrogenation step. The deethanizer insures final control of the ethane content of
the propylene product and the C3 splitter the propane content.
UOP has standardized on a single tower C3 splitter arrangement compressing overhead vapour before condensing to provide the
heat input needed at the tower bottom. (Product is withdrawn part way down the column to insure purity, a small overhead
recycle removes ethane and other trace contaminants.) This arrangement results in lower temperatures and enhanced distillation
properties than normal distillation, and avoids a two very large tower arrangement. The C3 splitter will still be in order of 60
meters tall and have up to 250 or so specially designed trays.2 The reboilers will also be special to minimize vapour compression
requirement. The C3 splitter will be more complex than for chemical grade, but in a new propane dehydrogenation system, the
added costs are more than repaid in the premium for PG product. Chemical grade product could be produced in such a system
with lower compressor energy inputs, if desired.
It is also very realistic to integrate the deethanizer/C3 splitter system with homopolypropylene production to handle the purges of
that process. Similar fits with other propylene derivative facilities may also be available.
The furnaces in the dehydrogenation system produce large qualities of steam—usually used to drive the compressor(s) in the
dehydrogenation system. The heat pump compressor of the C3 splitter is usually electric. There are major opportunities for
utility integration with other process plants and/or cogeneration facilities.
2
UOP has supplied the special trays to over 150 C3 splitters, most produce polygrade product.
Polymer
Guard
Grade
Treating
Propylene
Product
Product Rail Loading
Storage
Truck Loading
Off-specification propylene is assumed routed back to in process or to raw feed caverns in the byproduct case or sold as chemical
grade via direct railcar loading in the propane route. Note that any/all chemical grade shipments will have their own pipeline
system.
Two caverns will be needed with their own brine system (separate from other cavern systems to preclude trace impurities). As
with ethylene the cavern capacities must allow for at least a one-month supply shutdown and a one-month demand shutdown,
with flexibility for day-to-day and week-to-week supply/demand in balances. Brine displacement will introduce contaminants
such as oxygen and a special drying/chemical treating system will be needed to insure delivered product quality. A final
drier/treater will be recommended at any consuming facility to reinsure polygrade product quality, but is probably not needed for
chemical grade product.
Both railcars and trucks will be dedicated to the specific product grade. Rail car unloading facilities will be provided at one or
two spots for off-spec returns and to allow railcars to be used for peak storage.
Reference (a) contained an early 1999 estimate of USGC costs for propane based propylene units producing 150 to 350-kty,
starting up in 2002. Here, only the latter size has been considered – for two minimum sized derivative units and to take
advantage of Alberta’s high propane availability. Nominal capacity of such a facility is unlikely to be discounted, given
sufficient product storage capacity – say two months of production – to handle propylene and conversion units operating cycles.
Propane feedstock cost is discussed in the next section, here the production costs are considered.
An SIA or AIH location has been assumed with essentially identical capital costs as on the USGC – given optimum use of
prefabrication and excellent project management.3
Added feed processing needs and salt cavern product storage have been added along with a nominal adjustment to ‘other costs’
for corporate costs and land. Note that no synergies with other plants were considered, conversely, no hydrogen purification
facilities are included.
Hydrogen recovery and sale would add capital but add very roughly $1 million a year to the plant’s margin not considered here.
Converting the capital costs to annual ‘cost’ at a simple 20% per annum to cover provides the next table.
The original paper numbers would indicate a USGC facility production at 10.1 cents U.S. per pound, marginally lower at a 20%
simple before tax. (The early nature of these calculations is to be noted.)
3
A current study for AED indicates AIH petrochemical facility capital costs 5% below those of the USGC. Such a credit has not been
shown in these estimates.
The Mt. Belvieu (USGC)/Edmonton propane posting differences are related to the traditional ‘eternal triangle’
between Edmonton (the net producer region), Sarnia (eastern consumer hub, including Marysville, Michigan) and
USGC (the ‘mother-of-all-consumers’). The economics can best be conceptualized as propane prices being set by
the ability of USGC to ‘clear’ propane (at a profit over cracker feedstock values) into the Eastern U.S. market base,
via TEPPCO pipeline and local distribution) where they meet Sarnia and Marysville-based rail transported LPGs. The
combined transportation costs to that Eastern market base being about the same from both hubs, means that the
Sarnia area and USGC prices are about the same level, with seasonal variations. Conway, Kansas is the fourth hub,
sitting on the mid-western side of the triangle, and having a major ‘intermediate’ influence on the pricing dynamics.
Edmonton pricing discount (relative to these markets) is a function of rail or pipeline transportation costs to the
alternative market. Using Sarnia as an example, the discount is approximately the cost of shipping the marginal
barrel in the Cochin pipeline at non-incentive rates, or about 7 to 8 cents U.S. per U.S. gallon. A similar rationale
applies to the Edmonton long-term differential of about 7 to 8 cents U.S. per US gallon.
This study analyses have not considered the future in-depth, but foresee no major changes in propane availability, currently about
25,000-m3/d from Alberta gas and straddle plants, and refineries.
Reference (a) presents a week-by-week analysis for the period 1981 through part of 1998, showed a $217 per tonne (9.8 cents
U.S. per pound) differential between USGC propane and propylene over that period. That number is significantly higher than
noted in the above table – noting a major need for much more rigorous analysis by any propane dehydrogenation project
proponent.
Over 80% of Alberta’s average (25,000-m3/d) of propane production is sold out of the province, largely by pipeline. As noted
above, 350-kty propylene propane to propylene facility will only use approximately 2,150-m3/d (14,000-BPD). Thus, no impact
on Edmonton postings is foreseen with such a new local propane derivative plant.
Commercial propane has 2+% ethane and 3 to 5% butane contents. In the selected technologies the ethane would be routed to
fuel gas, there not being sufficient for economic recovery for sale. The C4’s would be isobutane rich and, with a small byproduct
stream from dehydrogenation valued above conventional butane (of special value to refinery alkylation units). Thus, no
adjustments for commercial propane impurity values have been made.
Commercial propane contains sulphur compounds above the <1-ppm level required by the dehydrogenation facility. But aside
from feed desulphurization drying and C4 plus rejection (in the feed depropanizer), feed propane treating needs are minimal.
The propane portion of the dehydrogenation feed is converted to propylene at approximately 94.5 weight percentage yield –
hydrogen at 3+% being the principal byproduct. In other words, 1.06 pounds of propane are required per pound of propylene.
Thus, deliberate propane conversion to propylene does not appear attractive with 1999 conditions. However, the difference
between the reference’s, USGC propylene, minus propane differentials and this study’s costing may warrant a second look. The
high sensitivity to capital is to be noted and hopefully, decreasing capital costs could make this route a future winner in Alberta,
even with our high propane costs, relative to developing country supply.
While this study did not find propane dehydrogenation greatly economic in a current Alberta setting – only a fair return even at
1999 USGC propylene value – the current surge in dehydrogenation technology development is to be noted. The two Mideast
projects committed to new technology may confirm lower capital costs, particularly in smaller facilities. The competition is
heating up with another technology entry about ready to go. Thus, while apparently poor economically at this time, the study
team strongly recommends very close attention to dehydrogenation developments and Alberta propane cost. We believe a
prudent propylene supplier or bulk user would go much deeper into dehydrogenation than possible in this study.
In the analysis of the chemicals derived from propylene or secondary products from propylene derivatives, the products are
handled in roughly the order below.
The resin is made from PG propylene in a gas-phase process. Some plants can use lower grade propylene – chemical grade – but
give up some capacity utilization with that decision.
In the gas phase process (Unipol PP from Union Carbide Corp., now Dow Chemicals) a fluidized bed reactor using a proprietary
catalyst is used. Melt index, isotactic level and molecular weight distribution, are controlled by catalyst type and quantity, as well
as the addition of molecular weight control agents.
The reaction takes place at 35 bar and 70ºC. The reaction gas is circulated by a centrifugal compressor, which also fluidizes the
bed and provides the feed stream. The reaction is exothermic, and the outlet gas removes the heat of reaction. Approximately
20% of the feed is reacted per pass. The granulated product is removed after cooling. Unread reactants are recycled.
Hydrocarbons remaining in the product are removed by purging with nitrogen. The granulated product is sent to a pelletizer,
which provides a uniform low dust product.
Both homopolymers and copolymers with ethylene or butene can be produced in PP plants. However, impact grade copolymers
require a second reactor.
4
BASF – the world’s largest chemical company, is now becoming a partner in Montell.
Plant Size
Although, the existing plants are in the 30 to 300-kty capacity a World Scale Plant should be considered to be in the 200 to 300-
kty range depending on process and propylene cost. The very minimum plant size for new facilities is at the 120-kty level.
Process Suppliers
The popularity of PP resins has help to foster a number of suppliers of process technology. However, three processes tend to
dominate the field – Unipol PP, Spheripol, and Novelen.
Unipol PP Process
From Union Carbide Corp. (now Dow Chemicals) this gas phase process is the most successful process and is readily available
commercially. Today 34 lines are operating or under construction worldwide ranging from 80 to 260-kty. This covers a wide
range of homopolymers and copolymers with up to 12% ethylene or 14% butene.
Spheripol Process
Montell PP (from Shell) is the main commercially competing process originally developed by Montedison of Italy. Shell recently
acquired all of the company and its polymer technologies. This process uses a liquid phase reaction and Montedison developed
the Loop Reactor. Some 65 Spheripol plants are in operation with a capacity of 10 million tonnes per year with individual plant
capacities in the 40 to 300-kty range.
Novelen PP Process
This process was developed by Targor (the PP Company with the BASF and Hoechst plants) and is offered exclusively by Krupp
Uhde of Germany. Some 39 lines with capacities of 60 to 225-kty are in operation or under construction. This process uses a
vertical helical stirrer for homogenization and is particularly suited for making rubber copolymers
Should growth rates in resin demand hold up, all the planned capacity is likely to be completed. The major change in the PP
business is the entry of Dow Chemical and Arco Products. Both firms have strong molding resin businesses, and PP is a natural
addition to their product slate. Also, Dow has a strong position in metallocene catalyst technology, and will likely put it to good
use in making PP resins.
Dow Chemical's first PP unit was a 200-kty at Schkopau, Germany. A second plant is slated for Tarragona, Spain, and a further
PP plant is planned for the U.S. The three plants together would give Dow a total of about 680-kty of capacity.
Dow Chemical’s move into PP and its plans for a resin plant in North America would offer solid potential to persuade the
company to investment in the province. A second possibility is Montell, controlled by Shell Chemical, which has a plant site in
the province (with BASF as a new partner). Montell has not been making capacity additions recently, and the firm may be
considering new capacity should PP market growth continue.
Nylon demand is the larger market segment as ACN is turned into adiponitrile for producing this plastic. Acrylic resins are also
made from ACN for fibers along with sheet production and molding grades. Nitrile elastomers also have a fiber market use as
well as molding applications. At the performance fiber end of the scale, ACN is used for making carbon fibers.
The plastics sector forms the second major use area for ACN derivatives. The chemical forms the ‘A’ in ABS and styrene
acrylonitrile (SAN), two copolymer resins. ABS is used in everything from auto parts and other molded products to pipe, while
SAN goes into the packaging sector as well as consumer food wraps.
DuPont’s nylon business is supported by the Beaumont plant, but it also buys on a merchant basis. Sterling and BP Amoco have
about 60% of ACN capacity for merchant sale.
The reactor effluent after cooling is sent to separator where unconverted propylene, nitrogen and combustion products which are
sent overhead. The bottoms product containing an aqueous solution of ACN is sent distillation for separation of acetonitrile and
purification.
Sohio are also developing a competing process based on propane feedstock, which claims to reduce the cost of production by
20%. This is based on the much lower price of propane compared to propylene. This process, when proven, will reduce the
propylene feedstock requirements for ACN.
Plant Size
Process Availability
The Sohio Process from BP Amoco Chemicals is the sole commercially proven and viable process at present. (A competing
process based on propane may also be licensed by the same party, as well.) Since BP is a major producer of this product, it
should be expected that the licensing for this process can be considered restricted.
Monsanto has an ACN process, which recently was licensed to Tae Kwang in Korea. This move breaks the near monopoly on the
BP Amoco process.
Solutia (formerly Monsanto) has an in-house ACN process, which they are using for the 300-kty capacity plant at Alvin, TX, but
it is not available commercially.
Domestically construction and durable goods – such as automobiles and major appliances – have kept ACN growing at 2 to 3%
annually. The fastest growing market for the chemical has been the polyacrylamide polymers that go into the paper and water
treatment business as flocculants and retention aids. PAM products have been growing at 4 to 5% annually.
On the supply side, there has been rationalization of ownership in recent years as Cytec sold off its fiber plants to Sterling in
1997. BP added a new production train to its Green Lake plant in 1996, which added 120-kty to the site capacity. Since then, no
new capacity has been added in North America.
On the raw material side, Alberta has both propylene and ammonia at fully competitive levels. Given the seasonable nature of the
ammonia business local fertilizer plants should be in a strong position to supply a world-scale ACN plant. With Agrium and
Sherritt in the AIH (and Agrium and Canadian Fertilizer at other sites) as ammonia suppliers an ACN plant will be well supplied
with ammonia.
The byproduct cyanide offers good market potential as well. Traditionally this side-stream has been converted into sodium
cyanide for the mining sector. In Canada, all the gold and copper refineries operate on imported sodium cyanide – mainly from
ICI, Degussa and DuPont. The western mining market in Canada as well as into the U.S. would be open to an ACN plant. The
nearest competitor is a liquid plant of FMC in Wyoming that supplies the local gold mines.
One of the more interesting potentials lies in production technology. A couple of years ago BP Amoco started of a demonstration
unit for its new process for producing ACN directly from propane. The process is said to cut the cost of acrylo manufacture by at
least 20%. Again, Alberta has a sufficient supply of propane to support a competitively sized facility, if the process shows
promise.
Virtually all cumene produced is oxidized to cumene hydroperoxide, which is then cleaved catalytically to phenol and acetone.
Therefore, the market for cumene is phenol.
The market growth in the U.S. has been driven by the growth in three major plastic resins – epoxy, nylon and polycarbonate
resins. Bis-phenol A is used for making epoxy resins and polycarbonates, as well as other chemicals. These two resins are
undergoing strong growth at present. Polycarbonate is being driven by its use in glazing as well as in compact discs, while epoxy
resins are finding greater use in industrial and consumer applications as adhesives, coatings and casting compounds.
Other demand areas for phenol lie in the wood binder business where phenolic resins dominate for outdoor grades of plywood
oriented strand board and increasingly manufactured studs and beams.
The integration of cumene and phenol production runs just over 20% of phenol capacity, which is very low for a commodity
chemical of this volume. Georgia Gulf is integrated from cumene into phenol in order to supply its phenolic wood binder plants
scattered across the continent. JLM Industries, Shell, Sun and Texaco are the other firms integrated back to cumene, but most of
their sales are into the merchant markets. GE Plastics has captive uses for phenol in its plastics and specialties business.
Kalama Chemicals in Washington State produces phenol from toluene, using an old process developed originally by Dow
Chemical, the plant also produces a series of benzoic acid derivatives.
Consolidation has been occurring in the phenol business. The most recent shift saw Sun Chemical buy Allied-Signal’s phenol
business, which tied phenol production to Sun’s cumene capacity in the Philadelphia area.
Liquid propylene is mixed with fresh and recycled benzene and fed to a fixed bed alkylation reactor. A proprietary regenerable
zeolite catalyst is used for the alkylation. The propylene reacts completely and the effluent flows to the depropanizer column
where the propane leaves as the overhead product. The bottoms are sent to the benzene column where the unreacted benzene
leaves as the overhead product and is recycled. The benzene column bottoms are sent to the cumene column where the overheads
are the cumene product with 99.7% purity. The bottoms are sent to the heavies column, where the overhead product is
diisopropyl benzene, which is recycled and the heavies are a byproduct.
Plant Size
• The existing plant capacities cover the 100 to 600-kty range. A world scale plant today should have a minimum
plant capacity of 300-kty. This would require the availability of 195-kty of benzene and 210-kty of propylene.
Plants are usually located near an existing refinery complex where the bulk feedstocks and utilities are readily
available over-the-fence.
Process Technology
• Cumene process technology is readily available on a commercial basis with three major suppliers actively
marketing their engineering and process expertise.
Mobil/Badger Process
• Provided by Raytheon, Pittsburgh, PA this is the traditional favorite and is well suited to low purity propylene. It
is commercially well developed and seven plants have been installed since 1996.
CDTECH Process
• This process has been developed by ABB Lummus and CR&L. This process uses catalytic distillation and is
suited to lower capacity plants. The first commercial unit of 270-kty for Formosa will go on stream this year.
Phenol
• Cumene peroxidation process is the major process used and involves the liquid-phase oxidation of Cumene into
Cumene hydroperoxide, which decomposes into phenol and acetone. For every tonne of phenol produced 0.6-
tonnes of acetone is generated in the process.
Plant Size
• A World Scale phenol plant would be minimum 150-kty and more likely 200-kty for most market areas.
Process Availability
• There are two major suppliers of phenol processes, Kellogg and ABB Lummus.
Kellogg/Hercules/BP Process
CDHYDRO Process
• ABB/Lummus’ process is a companion to its cumene technology and offered by CDTECH. Presently two plants
are being built – one in North American and the other in Taiwan and the firm boasts 50 years of building these
plants.
Phenolchemie, a Degussa-Hüls subsidiary, is a leading European phenolic resin producer, has announced plans for a facility in
Alabama. Also, Solutia’s new plant in Florida will have JLM Industries as a partner to take a portion of the output. That facility
will use Russian technology to produce phenol without going through the Cumene step.
Over the past year, the phenol industry has announced expansions that will more than double North American output, if all the
plants are constructed. To this point, the ‘brown-field’ expansions have been going ahead strongly. Suncor brought on stream the
Allied Signal expansion after its acquisition of the Allied facilities. Several of the other plants have debottlenecked to add some
capacity.
Cumene production capacity is out of sync with phenol at this point. Minor plant expansions and one new production train have
been completed in the past three years. Should the Cumene process continue strongly, and the proposed phenol plant capacity be
constructed there will be a shortage of Cumene in the coming years.
The development of technology that produces phenol without generating acetone is a big plus for potential investment in Alberta.
There are few acetone uses in Western Canada, and the newer technology would mean that byproduct acetone would not have to
be shipped out of the region by a plant mainly involved with supplying the phenolic resins sector.5
In Canada demand for phenol is supplied by imports, and the bulk of supply comes from the U.S. The share of the market held by
U.S. producers has remained constant over the years, in part, because of the spread-out nature of the domestic market. Major
demand lies in Ontario, Quebec and the Maritimes, but it is also scattered into Alberta and BC.
5
Acetone can be converted to isopropanol and most of that back to propylene via hydrogenation to alleviate byproduct challenges, if
required.
Dipropylene glycol
Propylene glycol
P-series Glycol ethers
5.5.1 North American Market for Propylene Oxide (PO) and Glycol
The major use of PO lies in the production of urethane polyols. When reacted with isocyanate the polyols make urethane foams –
flexible and rigid. On a PO basis flexible foam polyols account for 53% of use, while the rigid foams take 6% of PO and non-
foam use of polyols accounts for 1% of material going into this market area.
The next largest demand area for PO is the production of propylene glycol, followed by the p-series glycol ethers, miscellaneous
applications for PO, including making polyalkylene glycols, alkyl alcohol and isopropanolamines. Trade in PO per se is modest
with some 200 to 210-ktonnes being exported from the U.S. and imports into the U.S. being negligible.
The largest polygrade (PG) market is the polyester resin systems for making fiberglass parts; followed closely by antifreeze and
deicing fluids, where PG competes with ethylene glycols. Aircraft deicing and long-life radiator antifreeze applications top this
market area. In the food, drug and cosmetic areas, PG acts as a texturizing agent, binder, and humecent. Unlike ethylene glycol
The dipropylene glycol applications are a refined sub-set of the PG market. Plasticizers are the largest application area; followed
closely by unsaturated polyester resins. The other uses areas are cosmetics, urethane polyols, alkyd resins and a variety of areas
including functional fluids.
Plasticizers, 38%; unsaturated polyester resins, 23%; cosmetics and fragrances, 10%; polyurethane polyols, 8%; alkyd resins, 7%;
miscellaneous, including solvents and functional fluids, 14%.
Propylene glycol tends to be an integrated product to PO production. However, two of the propylene glycol producers are not
integrated with the production of PO, Eastman and Olin purchasing their raw material on a merchant basis.
Specialty products generated as byproducts from propylene glycol production are the di and tri glycols at about 10% of PG
production.
The traditional route is from propylene and chlorine using the chlorohydrin route. The dilute chlorohydrin is reacted with 10%
slaked lime (or caustic soda) slurry to produce PO; however, further reaction to the glycol is to be prevented.
This process gave way to the generally lower cost peroxidation route: peroxidation of isobutane and propylene to give PO and
tertiary butyl alcohol (TBA). This was traditionally done using air, but the newer plants use oxygen.
In a third process, propylene and ethyl benzene are reacted to produce PO and Styrene Monomer (SM) in another emerging
technology – the most common in new facilities of the past five years.
Chlorohydrin
The traditional route is the production of PO from propylene via the chlorohydrin route. This route has been used by Dow but has
a higher per capita propylene consumption.
The process uses the hydrolysis of propylene and chlorine with water in the presence of a lime slurry or caustic soda to produce
PO. The oxide must be removed rapidly to prevent the formation of propylene glycol. Propylene, chlorine and water are sent to
the reactor. Initially hypochlorus and hypochloric acids are formed. The liquid effluent contains 3 to 4% chlorohydrin. The
chlorohydrin should not separate as an oil phase as this increase the side reactions. Unreacted chlorine and acid are scrubbed
using a lime or caustic wash. The chlorohydrin is reacted with a 10% lime slurry or caustic solution to give PO and CaCl2 or
NaCl. The PO has to be removed rapidly from the reaction zone to prevent the formation of propylene glycol. The resulting PO is
purified by distillation.
Product Consumption
Propylene (100%) 940-kg
Chlorine 1,590-kg
Lime 1,090-kg
Byproducts are 90-kg of propylene chloride, 20-kg of ethers and 2,150-kg (as 1,005 CaCl2) of calcium chloride brine (or sodium
chloride brine).
Peroxidation
In this process isobutane is peroxidized at 90ºC and 450-psig in the presence of a catalyst to form tertiary butyl hydroperoxide
and tertiary butyl alcohol (TBA) yield is approximately 94% of the theoretical and 2.2-kg of TBA is produced per kg of PO.
Other byproducts depend on isobutane purity.
Input Quantity
Propylene 728-kg
Isobutane 2,160-kg
Oxygen 895-kg
Plant Size
For the peroxidation process, a world-scale plant has 300-kty of capacity. The World Scale plant based on the POSM process is
approximately 250-kty of PO plus 600-kty of styrene.
Union Carbide and Dow Chemical have PO technology but do not offer it on a merchant basis. Carbide developed a peroxidation
process using oxygen, which has equipment cost reduction, as well as higher conversion compared to air peroxidation. Overall,
the technology is not freely available and will require negotiation.
Propylene Glycol
Propylene glycol is produced from PO and water. PG can be produced in a stand alone unit starting with purified PO or in an
integrated unit using aqueous solution of PO, hence, saving on purification. However, it is the PO, which is a consumer of
propylene and not PG directly.
The process is similar to that used for ethylene glycol. It is in principle possible to use the ethylene glycol hydration facilities to
produce PG. In addition to mono propylene glycol, there is some requirement for dipropylene glycol for the polyester resin
industry.
PO with an excess of recycled water is heated to approx. 190oC at 185-psig. In the tubular reactor, total conversion to propylene
glycols takes place. Excess water provides for a higher mono glycol product.
Excess water is evaporated in multi stage evaporators, with the last evaporator producing low-pressure steam. The process is non-
catalytic. Crude PG is purified using a vacuum column. Dipropylene glycol can be produced by the addition of PO or by reducing
the recirculating water.
Plant Size
Since the propylene consumption is dependent on the PO plant size the minimal size is more a function of whether the plant is
stand alone or integrated. Scale can be further reduced in principle if some ethylene glycol equipment is used. However, it can be
said that the minimum capacity should be 40-ktonnes with an optimum for a standalone unit at 100-ktonnes.
Process Availability
With the similarity of ethylene and propylene glycol plants, there are several suppliers of PG processes and access is good.
Shell International have 60 EG and PG plants in operation and commercially offer the process. Sharing the field is Scientific
Design with again, 60 EG and PG plants in operation. The two other major glycol producers with well-developed technology are
Union Carbide and Dow Chemical (now all Dow). At this point, they do not appear to offer this technology for third party usage.
Durable goods such as cars, major appliances, carpeting, etc. that use urethane polyols are expected to be the major driver in
North America for PO in the coming years. At this point points strong automotive sales are driving flexible mold urethane foams,
while good demand for furniture, carpet underlay and bedding raises urethane slab stock requirements.
PG’s outlook is for growth in the 3 to 4% per year range, about 1% above PO’s growth rate. Unsaturated polyester, resins,
personal care products and functional fluids are considered the strong market areas for the chemical. In recent years the strong
polyester resins business has helped growth, but in recent years, dicyclopentadiene-based resins have been moving into the
fiberglass business. This trend may cut the use of PG in this market segment. Deicing fluids for aircraft using PG have been
growing nicely due to the concern about toxicity for using ethylene glycol. Growth of USP glycol in the cosmetics and the
personal care segment is being driven by strong markets for a variety of skin care and sunscreen products; however, tobacco use
is expected to continue to decline.
U.S. Exports of propylene glycol have been in the 80-kty level recently with imports minimal.
5.5.5 Potential for Alberta with Propylene Oxide (PO) and Glycol
A PO/PG complex likely would have to be considered, to justify building a Greenfield plant in Alberta. Favorable raw material
supply helps, but developing market access to the Asian markets and strong ties to U.S. mid-western consumers of both PO and
PG would be critical in justifying an investment in these chemicals in the province. The Canadian market does offer some
demand support, although most of the use lies in the eastern half of the country. Between the two chemicals domestic use run in
the $100 million level annually.
Asian PO demand, which had been growing at double-digit rates, is still expected to increase by 4 to 5% this year and offers
interesting potential. It is likely that an investor will have a specific geographic supply need to seriously consider a PO/PG
facility. Also, many of the producers are moving into value-added products such as polyalkylene glycols – e.g., Dow recently
expanded its capacity for those products at its Plaquemine, LA site.
Demand for P- and E- series glycol ethers is about 880 million pounds per year and growing at 2 to 3% per year. The coatings
industry consumes about half of the glycol solvents. Because P-series are not classified as hazardous air pollutants, they will
continue to outpace demand for E-series and hydrocarbon solvents.
All the major producers provide a range of products to the coatings, adhesives, inks and general solvents business areas. Also, in
their production complexes they also produce various alcohols and PO to support the production of the propylene and other
ethers.
Propyl ethers are produced by the dehydration of propyl alcohols. For this, IPA is a suitable feedstock.
The traditional propyl ether process is carried out in the liquid phase using sulfuric acid as the dehydrating agent. A 96% sulfuric
acid is reacted with an aqueous 95% IPA solution in a corrosion resistant kettle. The reaction takes place 125oC. The vapor
effluent is scrubbed with dilute caustic soda to remove the residual acid. The ether is recovered by distillation. The process
requires special technology due to the explosive nature of the ether. The scale of production is normally about 10 to 15% of the
IPA capacity.
The production technology is similar and the same plants can be used for making a variety of ethers. Ethylene, butylenes and
methylene ethers are made by the same producers.
5.7 n-Butanol
Normal butyl alcohol or n-butanol is a medium-volume propylene derivative that goes into solvent products on a direct basis or
as a raw material.
Most commercial production involves the hydrogenation of n-butyraldehyde made through oxo reaction with propylene.
However, there are byproduct sources as well. Condea Vista Company produces about 5-kty of n-butanol annually at Lake
Charles, LA as part of its detergent alcohols operations. BP Amoco obtains an ethanol/n-butanol stream as a byproduct at its
Pasadena, TX linear alcohols plant.
The option is to use the oxo synthesis to produce butyraldehyde, which can be hydrogenated to butanol. The alternative product is
2-EH, which is produced by the aldol condensation reaction followed by catalytic hydrogenation. In the newer processes,
propylene and syngas can be converted directly to a mixture of n and iso butanol and 2-EH without isolating the butyraldehyde.
A mixture of n and iso-butyraldehyde can be produced by the LP Oxo Process, available from Kaverner/Dow UCC using a
rhodium catalyst, which operates at less than 300-psig as against the 1,500-psig for the convention oxo process. The oxonation
process produces n to iso product at a ratio of 10 to 1, but can be tailored to ratios varying from 30:1:1. The mild reaction
conditions result in fewer byproducts. The catalyst has a long life and is regenerable at site. The water-soluble Rh catalyst is
easily recovered and reused. The reactor effluent is cooled and crude product separated with recycle of unreacted gases to the
reactor. N and iso butyraldehyde is separated by distillation. A separate syngas generation facility based on natural gas feed
would typically be required, but H2O and CO can be made available from hydrogen and methanol units now in the AIH and SIH.
N-butyraldehyde can be hydrogenated to produce n-butanol using a variation of oxo alcohols synthesis. This uses a propylene:
CO: H2 mole ratio of 1:1:2. The reaction takes place at 1,000-psig and 150oC. The catalyst is a Ni catalyst in the Celanese/Rhone
Poulenc process. This process requires a significant supply of hydrogen.
For the direct process from syngas that generates both n-butanol and 2-EH the inputs are as follows for Butanol.
Table 5.7.3-3. Raw Materials Inputs per 1,000-kg of Butanol from Syngas
Input Quantity
Propylene 1,050-kg
Syngas ( CO + H2) 17,000-scf
Hydrogen 5,000-scf
Plant Size
Plants of capacity 30 to 350-kty have been installed. The minimum capacity for a world scale plant starting from propylene is
150-kty capacity. For 2-EH production, this could be reduced to 50-kty.
Process Availability
The process options for making n-butanol are several and the process can be combined with the production of 2-EH and other
oxo alcohols.
Kvaerner/Dow/UCC have a well-developed LP oxo synthesis for the production of butyraldehyde. This is the rhodium catalyst
system described above. There are 18 plants with capacities up to 350-kty installed.
Krupp Uhde offer a Ni catalyst based hydrogenation process, which is commercially available and well proven. They are also
leaders in syngas production and offer the adol route where butyraldehyde is treated with dilute caustic soda to give 2-EH.
Hüls AG offer the catalytic hydrogenation of butyraldehyde to butanols and 2-EH. The company has two plants in operation
since 1988.
Kvaerner/Dow – UCC also offer the Rh catalyzed low-pressure oxo process, which has been installed at Taft for Dow-UCC.
Celanese/Rhone – Poulenc also offer the Rh catalyzed process for direct oxo synthesis of n-butanol from propylene and syngas.
Shell Chemical has a one-step process, which converts propylene to butanols or 2-EH by hydrogenation. This is a flexible
process and permits flexibility in operations depending on market demand. This process has restricted licensing possibilities.
The use of butanol in acrylate and methacrylate esters is growing at above 4% annually. These applications are expected to drive
the market in the coming years. They now account for over 40% of n-butanol consumption. Both of these products go into the
construction renovation market as an additive for latex paint. The additional growth potential lies in the shift to water-based
coatings in the paint industry on an overall basis. Exports of n-butanol derivatives – butanol, butyl acrylate and butyl acetate –
have become increasingly important. However, new global capacity may reduce the volume in the coming years from the U.S.
The domestic demand for n-butanol runs in the 5 to 6-ktonnes range annually and the value of imports has been in the $4 to 5
million level, not major support for a plant investment.
Overall, the potential for production of n-butanol in Alberta is modest. Coupled with an AA and acrylate facility the potential
rises dramatically, but as a single product, the investment potential must be considered fairly low.
About three-quarters of AA production is converted directly into acrylate esters on site and the balance is purified and sold as
glacial AA. Despite, nominal U.S. over-capacity AA imports exceed exports.
The reaction between propylene and oxygen is carried out in a catalytic reactor at 400oC containing a solid, cobalt
molybadate/tellirum oxide catalyst. The reaction requires careful control to prevent by product formation. Aqueous AA is
separated and concentrated to crude AA. For ester production, this can be reacted with the appropriate alcohol in a n esterification
tower using an acid catalyst. A vapor phase esterification process using silica gel has been developed for ethyl acrylate. This has
a conversion rate of 56% at 260oC. This has the advantage that for an integrated plant the heat efficiency is greatly improved.
However, for product quality considerations most new plants use glacial AA as the starting point for the esters.
Plant Size
A World Scale Plant for this process has a capacity of 200 to 300-kty.
Technology Availability
Most of the producers of AA are reported to license their technology for selected markets. There are three or four firms offering
that technology on a commercial basis. BASF, Nippon Shokubasi and Mitsui tend to be the leaders in this production technology
area.
Currently the firms expanding in AA tend to be using their own technology. BASF is setting up a plant in Malaysia (a joint
venture with Petronas) using in house technology. Sumitomo is providing the technology for a 25-kty glacial AA plant in
Singapore, while Nippon Shokubai/MHI are providing technology for a 40-kty acid and ester plant in China.
Mitsubishi Petrochemicals have provided technology for seven plants producing AA. The process boasts a high yield catalyst
system and low capital cost, but Mitsubishi does not seem to be involved in the latest round of global expansion.
To meet this demand outlook there has been some expansion of the supply. Slated for start-up in 2001 is a new 125-kty plant of
American Acryl at Pasadena, TX. The company is a joint venture between Elf Atochem North America and Nippon Shokubai.
Elf is also constructing an acrylate facility to take its share of the new plant’s output. Both BASF and Celanese has recently
added to the capacity of their AA plants, and Celanese is adding a further 80-kty at Clear Lake, TX later this year.
The players in AA and its derivatives also are changing. As a consumer of AA and acrylates in the U.S., Dow Chemical broke
ground in 1998 for a 125-kty AA unit at its BSL complex (Bohlen) in Germany. Startup of the project, which includes esters, is
scheduled for 2000. With the Dow/Carbide merger, domestic interest in the product could be increasing, since the Carbide plant
is the smallest complex in the North American industry.
5.9 Isopropanol/Acetone
Isopropyl alcohol or isopropanol (IPA) is a popular solvent.
The ability to make a high quality acetone from isopropanol has created a outlet for about 15% of IPA demand. However, in the
context of the acetone business IPA-based product accounts for only 5% or less of supply.
Household and personal care use of IPA represents sales to the consumer as a cleaning solvent and a medicinal alcohol. The
pharmaceutical use of IPA is as a process chemical or additive.
The production of acetone is dominated by the phenol plants where it is a byproduct or coproduct of the cumene to phenol
process. Deliberate IPA to acetone production is aimed at high quality markets where minor trace chemicals cannot be tolerated.
Isopropanol (IPA) production from propylene is produced via a gas phase 170 to 190oC temperature medium
pressure reaction over a fixed bed catalyst. Unreacted propylene and most byproducts are recycled. Propane and
Capital costs are in the order of $60 million for a 100,000-kty facility using Degussa technology. If desired ethanol
can be produced in the same facility with ethylene replacing propylene as feed.
Acetone
Approximately 27% of the IPA are used to produce acetone by the water removal step. However, 90% of the North American
acetone is as a byproduct in phenol production. A small amount is also produced as by product from PO production.
Plant size
Plant sizes vary widely depending on the local market for high quality acetone. A minimum plant size would be at the 25-kty
level.
Process Technology
IPA to acetone process technology is available from Edelneau of Germany, as well as IFP, of France. The bulk of acetone is
produced in the conversion of cumene to phenol, as discussed above.
Propyl Ethers
Propyl ethers are produced by the dehydration of propyl alcohols. For these derivatives, IPA is a suitable feedstock.
In the traditional process, this was carried out in the liquid phase using sulfuric acid as the dehydrating agent. 96% sulfuric acid is
reacted with an aqueous 95% IPA solution in a corrosion resistant kettle. The reaction takes place 125oC. The vapor effluent is
scrubbed with dilute caustic soda to remove the residual acid. The ether is recovered by distillation. The process requires special
technology due to the explosive nature of the ether. The scale of production is about 10 to 15% of the IPA capacity.
Plant Size
The capacity for propyl ether is in the order of 10-kty given its specialty chemicals nature.
Process Technology
Propyl ether technology is available from various engineering companies and major IPA producers have it for internal use.
Solvent demand is an area of little growth. The pharmaceutical industry, a major consumer, has been moving to solvent
recycling, which has cut into IPA sales. Regulations aimed at cutting down on volatile organic compound (VOC) emissions also
have been hurting IPA solvent use as industrial consumers move to less volatile products. Derivative products – amines, esters
and ketones – are growing at higher rates in the 3 to 4% annual level, but demand in those products is not offsetting a stagnant
solvent market.
Plasticizers and acrylates are normally major outlets for 2-EH. The balance of uses represents fewer than 10% of demand.
The plasticizer business has been dominated by phthalates. Today about 60% of the plasticizer EH goes into making dioctyl
phthalate, followed by dioctyl terephthalate (about 30%). The Plasticizers go mainly into the polyvinlyl chloride (PVC) business
for making flexible products. Acrylates are mainly used in emulsion polymers for adhesives, coatings and in textiles. The rest of
demand lies in making specialty chemicals used in the lubricant additives and surfactants or directly as solvents. On a net basis,
export account for about 15% of demand from the domestic producers of 2-EH.
All the North American capacity for 2-EH lies in Texas with Eastman accounting for half of the continent’s capacity. Aristech
and Union Carbide (Dow) rank second and third in the sector. Aristech’s Pasadena site also has an ophthalmic anhydride facility
or plasticizer production. BASF has been a major producer and developer of plasticizers, while Shell has strength in lube
additives and certain improvers as well as other specialty products.
There are three processes for making 2-EH: the oxo process, syngas and propylene, and the hydrogenation of butyraldehyde.
Table 5.10.3-1. Raw Materials Inputs per 1,000-kg of 2-Ethyl Hexanol by Hydrogenation
Input Quantity
Butyraldehyde 1,200-kg
Hydrogen 10,000-scf
It should be noted that approx. 200-kg of byproducts are obtained in the process.
There have been minor additions to 2-EH capacity in recent years, although much of the oxo plant capacity installed has been
oriented to n-butanol use. Eastman added about 40-ktonnes of capacity to its facility in 1997, but the other producers have
expanded their aldehyde capabilities without adding any hexanol capacity.
In Shell's one-step process, propylene is converted directly to butanols and 2-EH, without isolating butyraldehydes. The
company's 2-EH capacity is very flexible depending on the production of n-butanol, some of which is used solely for glycol
ethers.
Growth for 2-EH has been running in the 2 to 3% level and is expected to remain there. The plasticizer business has been under
pressure for the toxic concerns regarding phthalates. As a result, for many PVC applications processors have been moving to
other products away from the phthalates. Growth is acrylates and methyl acrylates is expected to be in the 5 to 7% range in the
coming years as demand for emulsions increases.
As part of a butanol/2-EH complex, production of this chemical could occur in the province. On its own 2-EH will not be a driver
for investment, despite the favorable supply of propylene in the province and the cetane improver market.
On an overall continental basis low demand growth and an in-place capacity of 500-ktonnes facing a demand of less than 400-
ktonnes and Asian imports means it is unlikely that a new plant will be built in the medium future. Pressures on 2-EH in the
plasticizer business may further reduce demand.
The soft and waxy resins are produced by PP and PE producers as specialty items in their product lines. Eastman Chemicals and
Exxon Chemicals both have substantial product lines going into the adhesives industry (hydrocarbon resins, solvents, additives,
etc.). The dominant position is held by Eastman, which supplies both APP and atactic PE as part of its adhesives chemicals
business.
About 15 to 20% of material comes as a byproduct from PE and PP plants. International Waxes of Ajax, ON was one of the
forerunners in developing the APP applications in adhesives, as an adjunct to its wax business (business sold to IGI
International). Firms such as Crowley Chemicals of New York also market byproducts from various PP plants.
APP, unlike resin grade PP, involves polymerizing propylene into a non-regular or random polymer chain. During the step-
growth polymerization process, an isotactic structure normally found in PP resins is not produced, and the result is a soft, waxy
product highly suited for blending into adhesive formulations. Raw material requirements are the same as for homopolymer PP
and identical production hardware is required.
From a capital cost point of view, an option is to obtain an old, small PP reactor that will be the right size for the market to be
served. The APP market could not take the output from a new large plant.
One additional factor in terms of technology acquisition in the context of a Alberta location could be the possible availability of
plant hardware. At the Shell/Montell PP plant site in Montreal is a mothballed PP plant with some 80-kty capacity. This facility
was considered at one point by its past owners to be reactivated for making APP.
The markets for APP and PE run in the 120 to 150-ktonnes (265 to 330 million pounds) area annually in North America.
The major application lies in the bituminous roofing materials, where APP competes with SBR rubber. The PP allows the sheet
roofing material to be easily adhered and bonded. The next major market lies in the formulation of hot melt adhesives. Along
with EVA resins and hydrocarbon resins, APP provides melt flow and body to the hot melt formulations.
Close to one-third of the APP market is in the manufacture of hot melt adhesives. This has been a steadily growing application
area for APP.
Paper lamination and some plastics/paper lamination is another solid use of APP. In the wire & cable area the resin is used for
cable flooding where the polymer is used to fill in around the insulation filler in large power cables to keep moisture out.
APP is also used in the lamination of plastic films and plastic to other materials. The miscellaneous uses, are in the wire and
cable industry where APP is used for filling and sealing the insulation in high-tension cables and other similar products.
As older PP plants are retired and the new PP technology generates no atactic byproducts, new capacity for atactic products will
be required.
As has been indicated in Section 4, refinery propylene can be upgraded from a ‘refinery grade’ to a ‘chemical grade’ or a ‘PG’.
However, some of the propylene sources, such as ethylene plants, generate diolefins and other difficult to handle products that
can hinder efficient use of C3 streams as propylene sources without further processing.
Selection Criteria
In rating the chemicals for investment potential in Alberta, four criteria were used to evaluate the prime propylene derivatives. As
has been indicated in the previous sections, many of the propylene chemicals are produced in a complex, so that several products
justify and carry the overhead of production. For an investment to be made in a propylene production facility in Alberta a two or
three-step production decision may be required to justify the expenditure, and such complexity mitigates against a Greenfield
investment.
Based on examining the eight primary derivatives analyzed in this study and considering the need for downstream investments to
justify an initial production facility, the rating is as follows:
Polypropylene offers solid potential in the medium term. Growth is high at 5 to 6%, and despite recent expansions in capacity in
North America, a need for further capacity is likely in the next 4 to 5 years. The capital investment in, say, 225-kty plant is not
large, running in the $175 to 200 million range. Sufficient raw materials are readily available to support a 225-kty facility. The
major negative is the regional market support. Product would be shipped to Asian markets or to the U.S. Midwest, so raw
material costs need to be low enough to cover transportation costs.
Alberta has sufficient raw materials for a world-scale plant. In addition some of the raw materials for making copolymer PP are
available in raw form, at last, in the province. PG material is required for an efficient plant operation.
While not considered in-depth a smaller APP project could well be developed for its niche markets.
Acrylonitrile has good potential through a supply of raw materials and a growing Asian market, which can be accessed in
competition with the U.S. exports from the Gulf Coast. There are sufficient raw materials to support an ACN plant, and chemical
grade material is all that is required, making the process competitive in the context of Alberta.
Cumene/Phenol is one of the strongest product potentials for Alberta on a market basis. There is strong regional demand and
little competition. Benzene raw material is a problem, which is why it does not rank in the top three selections for Alberta
potential investments. A growing regional market for phenol with only one small competitor is a major plus. Also, changes in
production technology mean that the product can be made without generating acetone as a byproduct. The lack of regional
acetone customers has always been a major deterrent to a cumene/phenol plant complex, but added processing can decrease that
risk. The only major negative lies in the tightness in benzene supply in the province. With sufficient propylene available for a 150
to 200-kty plant, some 100-ktonnes of benzene would be required.
Propylene Oxide
PO has perhaps the strongest potential in an Alberta context outside of the top four chemicals selected. Raw materials are
sufficient in the province to support a plant. However, PO on its own has little market potential, and a PO derivatives complex
has to be considered in order to create demand. Many of the key derivatives – urethane polyols, propyl esters and the like have
most of their demand far to the Southeast in North America, and in the early stages of growth in many parts of Asia. Propylene
glycol might be the derivative exception.
Isopropanol
From a production point of view, isopropanol offers good potential in Alberta. However, there is little regional market and the
low value-added of the product makes it difficult to ship long distances and be competitive. Should IPA find use in a volume
application in the region, the potential would increase substantially. There are sufficient raw materials around and the process can
be run with refinery grade material as feedstock.
n-Butanol
Butyl alcohol offers only modest potential for an Alberta investment. Any investment would likely have to be coupled with an
AA plant. There is little regional market and the export potential into the Pacific Rim countries is modest at this time.
2-Ethyl Hexanol
Ethyl hexanol is last on the list due to low growth rates on plasticizers almost globally, and little regional market to be accessed.
Canada did have a small 2-EH plant in Montreal some years ago, but it was closed with little disruption to domestic plasticizers
producers. From a market perspective, the plasticizer market is under pressure with the European Community threatening to ban
the use of phthalate plasticizers, particularly for use in consumer products such as kids’ toys. Also, local cetane improver 2-EH
nitrate markets.
An analysis of phenol is at the end of this section. This product has strong regional demand, but there is a shortage of raw
materials. The potential for a regional phenol plant is strong.
PP is made by polymerizing propylene into polymer chains of various lengths; copolymers are also produced by adding rubbers,
and various monomers to change the performance properties of the PP resin.
Capital costs and operating cost factors vary widely with the specific location and the service infrastructure available. Many PP
plant projects include propylene recovery on production as well, and there is considerable benefit to having a resin plant and a
fractionator located on the same site.
The major demand drive in the market for a Western Canadian plant would be a mix of continental business and some Pacific
Rim exports. Globally PP demand is running in the 23,500-kty (1997). Should growth continue in the 5 to 7% annual level about
five 250-kty PP plants are required each year to keep the global market in balance.
The high growth in the injection molding and distributor/compound market sectors in North American can be traced to these
developments. PP resin producers now are making copolymers with ethylene, butylenes and various rubbers with the
‘comonomer’ content running as high as 50% for some of the new rubber copolymers coming onto the market.
The PP resin producers are using different catalysts and comonomers to change stiffness, impact resistance, toughness, cold
weather cracking resistance and flow rate in their products. Most of these developments are finding they way to the injection-
molding field. Some of the new copolymer resins offer the benefit that parts can be painted directly out of the mold, eliminating
surface treatment.
As a result of the developments PP resin growth of 10% or even higher is predicted for the molded pails, jars, baskets, auto
fascias, furniture, appliance parts and some industrial products.
In comparison application, segments such as fibers and blow moldings are mature, even though their overall growth is high
compared to other plastic resins.
The Asian market is the largest PP market in the world with some 11,500-ktonnes of resin being consumed annually. With
relatively fast-growing markets in the region, the Pacific Rim has been an importer of PP resins in the 200+ ktonnes level
recently.
Now Exxon is planning 250-ktonnes of new capacity in Singapore, and there are several projects in the works in the Middle East.
That will supply some of the Asia-Pacific shortfall in resin, but still leave room for supply from North America.
The Canadian situation on PP resins exports has move from an export position to integration into the continental market. Shell’s
takeover of Montell brought both the Alberta and Montreal plants under one management and the move to more copolymer
production from the two facilities helped to shift the supply focus to the regional markets.
The cross-border trade on PP resins is a major factor today with Canada running a trade deficit on PP resins with the U.S. While
exports to the U.S. run to $243 million Canadian, imports from the U.S. run at $451 million Canadian on PP resins.
The export of PP resins from the U.S. to Pacific Rim countries amounted to $96 million Canadian in 1998. Canada and Mexico
accounted for almost 70% of the exports in that year. However, U.S. trade with the Pacific Rim countries over the past few years
has been declining. In 1995, shipments to Hong Kong, China and Taiwan accounted for 15% of exports, totalling $906 million
Canadian of business.
Metallocene polypropylene offers a narrow molecular weight distribution, which improves the properties of PP resins
considerably. While much of the PP markets are commodity oriented and some analysts do not foresee processors paying more
for mPP over conventional PP resins, the expectations are that mPP will have a dramatic effect on resin use for many products in
the coming years.
Another factor in PP plant technology is the reduction of capital costs on plants in recent years. The Unipol PP plant technology
was the start of this trend and recent facilities being built are coming in 10 to 15% lower than plants built five or more years ago
for the same capacity.
While a PP plant does not consume large amounts of electricity or natural gas there is some solid savings offers by most Alberta
locations. Labor costs in Alberta are slightly below the USGC for plant operating, while construction costs are generally
equivalent to 5% higher.
Reference: Alberta’s Petrochemicals – Transportation Assessment – Alberta Department of Economic Development updated to January 1999.
The transportation factors are such that shipping to Chicago is slightly uncompetitive compared to shipping out of Houston,
however movement to Asia is competitive on prices as well as shipping time. Shipping time from the Gulf Coast to Asian
through the Panama Canal takes 30 to 39 days, while out of the BC ports 15 days is shaved off the delivery typically.
Therefore, overall a PP facility located in Alberta will have a significant operating cost advantage over a Gulf Coast facility
competing in the Pacific Rim markets.
The large Asian market with its continued importation of PP resin is an essential business factor to consider. The ability to
competitively ship from Alberta to Pacific Rim markets makes a plant investment highly attractive to any firms wishing to
expand its business in Western North America and move more products to Asia.
ACN is made through the reaction of propylene, ammonia and air in the following reaction:
The yield on the process is 70 to 75% and refinery grade propylene and fertilizer grade ammonia can be used. Oxygen from air
is assumed here, but purchased oxygen for enriched air route is to be considered.
Plant capital and operating costs vary widely with location for ACN. When a plant is situated near an ammonia facility as in the
AIH ammonia will be pipelined and uncompressed for reaction in the ACN units with considerable cost savings all around. Also,
the handling of and reaction into sodium cyanide or disposal of the hydrogen cyanide can vary capital costs on a facility to a
marked extent.
The expansion of ACN capacity has been modest, although the plans are in place to meet some of the growing demand in Asia.
The new plant of Formosa Plastics in Taiwan was slated to start operation last year, but has been put off until the middle of this
year. In Korea the 250-ktonnes Ulsan plant planned by Tae Kwang has been put on hold or abandoned because of the financial
crisis in that country.
The major countries importing U.S. ACN are Japan, Taiwan, China and Hong Kong with smaller amounts going into India and
Thailand. Asian countries account for over 80% of the export trade from North American in ACN, and even with the expansion
of regional facilities, the movement from the USGC remains strong.
Taiwan
Other 21%
29%
Singapore
4% China
0% Korea
29%
Japan
17%
Canada imports all its sodium cyanide and an ACN plant would be able to serve the Canadian market as well as a portion of the
Western U.S. gold and copper mining areas. A world-scale plant would also have additional cyanide available to serve the export
markets for sodium cyanide in Austral-Asia and South America. The closest competitor in the U.S. is the Wyoming plant of
FMC, a liquid sodium cyanide facility serving that region’s gold mines.
Alberta has a good supply of sodium hydroxide from the Dow Fort Saskatchewan chloralkali plant, so all the elements to support
a cyanide business an ACN plant exist in the province.
On the negative side for propylene use, but a potential factor in the ACN business could be a new BP Amoco process, using
propane as a feedstock, instead of propylene and claims major savings in production.
Reference: Alberta’s Petrochemicals Transportation Assessment – Alberta Department of Economic Development update to January 1999.
For an Alberta ACN plant operational costs are competitive and infrastructure can help in the supply of services. Oxygen
pipelines are available should a plant want to use an enriched air stream in production. In addition, steam may be available ‘over-
the-fence’ in some locations. Electrical and natural gas costs offer solid savings compared to the USGC.
Labor costs in Alberta are slightly below the USGC for plant operating. Construction costs are generally, equivalent to 5% high.
The transportation factors are slightly negative for ACN, but in terms of serving the Pacific Rim markets, an Alberta plant would
have a good response time. Shipping time from the Gulf Coast to Asian through the Panama Canal takes 30 to 39 days, while out
of the BC ports 15 days is shaved off the delivery typically.
The possible need for storage on the West Coast requires further consideration.
A medium-scale, 250-kty ACN plant in Alberta would have solid market coverage in the Asian markets, and the ability to back
out some or all of the $150 million in exports to that region.
Perhaps the most favorable development scenario for an Alberta ACN investment might be a slowdown in Chinese investments.
The BP Amoco plant has been in the planning stages since 1996; such a facility could be ideal here to serve the Chinese market.
Recently Dow and Celanese joined forces to build an AA plant in Bohlen, Germany. Dow will use the bulk of the new plant’s
output and Celanese will sell the balance on the merchant market in Europe.
A similar joint venture might be possible in North America, and the companies have made initial moves in that direction. Dow
produces super absorbents and acrylic lattices both in Europe and North America, buying AA. In addition, an acrylic latex plant
is already located in Alberta and Dow has been considering its long-term future.
While there are several routes to AA the most favorable one for the Alberta area would likely be the oxidation of propylene to
acrolein, which is then oxidized with a molybdenum-vanadium catalyst to AA. Other routes such as reacting acetylene and
carbon monoxide run into the problem of local raw materials.
However, the Dow-Celanese venture in Germany is using the propylene route using Celanese process technology. Using
propylene feed from the ethylene crackers, the new plant will produce 80-kty (175 million pounds per year) of crude AA, which
will be processed into 60-kty (132 million pounds) one of either AA or butyl esters. The plant will be using Nippon Shokubai
catalysts.
AA is produced by the oxidation of propylene in the following two-step reaction that takes placed in the reactor:
C3H6 + O2 Æ C3H5O + H2O
2C3H5O + O2 Æ 2C5H8O2 + H2O
Capital cost on AA plants may vary with process. BASF has a new process, which they are planning to use in Brazil. This
catalyst technology developed by the German firm reportedly reduces capital and operating costs significantly.
The hottest market area for AA lies in the super absorbent polymer (SAP) business. These products have been growing at 5 to
10% annually as the chemical has found application in feminine products, diapers, wipes as well s medical products and a host of
specialty uses. Growth in super absorbents has been running close to 8% annually with no let up in sight. The European market is
showing sings of maturity, but growth continues at a good pace in North America. Highest growth for super absorbents occurs in
South America and in the Pacific Rim countries.
The global SAP business now is almost 750-kty of product with 38% of demand in North America and 32% in Europe. Japan is
the other well-developed market area. Latin America and Asia are the hot growth markets for SAP product with demand
increasing at 7 to 10% annually in these areas. Butyl acrylate is a major raw material for making super absorbent polymers.
The acrylates are experiencing slower relative growth, but still a solid 3 to 4% annually depending on the product. The major
driver for them has been the push to remove solvents from coatings, adhesives, inks and various industrial products. Concern
about VOC emissions has been pushing the formulators in these sectors to reduce or eliminate high volatile solvents. Acrylates,
along with ester solvents, can be a major part of the reformulation as well as performance improvers for making the thin films
required.
Ethyl acrylate goes into the acrylic resins sector, and this clear plastic has solid growth prospects in both casting and sheet
applications. However, demand is not likely to be beyond GDP growth in the coming years from the acrylic resin area.
Degussa-Hüls’ subsidiary, Stockhausen, has merged with Rohm & Haas’ AA business to form StoHaas. Rohm & Haas also
bought Stockhausen's butyl acrylate business, and the two firms are aggressively perusing a supply position with super absorbent
(SAP) producers around the world. The planned Brazilian plant is aimed at supplying a new Degussa-Hüls SAP plant.
Sasol's board has approved an R835-million ($140 million) n-butanol project and a plan to builds a world-scale acrylates complex. It
follows completion of a feasibility study launched at the end of last year (CW Dec. 9, 1998, p. 22).
Sasol will locate the 150,000-m.t./year n-butanol unit at either its Sasolburg or Secunda complexes. The company will make a decision
by March 2000 when it completes basic engineering work on the plant. Completion is scheduled for 2002. Sasol will supply the plant
with propylene and synthesis gas feedstock, which it produces at its coal-to-synthetic fuels plants. Sasol will locate the acrylates
complex at the same site as the n-butanol plant.
The complex will comprise an acrylic acid plant and units producing n-butyl acrylate, ethyl acrylate, and glacial acrylic acid. The
acrylates plants are likely to be commissioned in 2003.
All of the new plants will be operated by Sasol's solvents division. Once on stream, the n-butanol and acrylates units “will probably add
40%-50% to Sasol solvents' [$200 million/year ] sales," says general manager Anton Putrer. The n-butanol unit will use technology
licensed from Mitsubishi Chemical. Most of the n-butanol and derivatives will be exported, says Sasol. The company has also agreed to
supply a small portion of the output to Mitsubishi. – Chemical Week.
Dow Chemical also is planning to build a SAP plant in North American and apparently is considering an AA plant. No site or
timing has been announced.
In summary expansion of AA and acrylates is continuing on a global basis. However, the capacity gain in North America could
still leave room for a new plant in the coming years.
North America tends to be a net importer of AA, despite the strong exports in acrylates. Imports have been at the 70 to 80-
ktonnes for several years. Canadian imports of AA run to $3 million annually, but 90% of that is material imported from the U.S.
Japan is a major supplier of AA to North America with imports from Japan to the U.S. running as high as $60 million Canadian
in recent years.
The acrylates offer strong potential for import substitution into North America. Canada brings in $1 to 2 million worth of
acrylates not including material coming up from the U.S., which runs to $45 to 50 million annually in recent years.
Japan and Mexico account for over half of the imports of acrylates into the U.S. and form the major potential for import
displacement. The European suppliers, including some material form France, England and the Netherlands, also could be
displaced by new North American capacity in the coming years.
Investment in an AA plant and most likely an associated acrylates facility would be raw material competitive with the other
plants on the continent, and should be competitive in much of the continental market.
Table 6.4.4-1. Competitive Cost Factors for Acrylic Acid Production in Alberta
Factor Difference to USGC
Raw Materials
- propylene - 2 cents/kg
Capital Cost - 5 to 0%
Plant labor & operating costs - 2 to 4%
Electrical costs - 1 cent/kWh
Natural gas costs - 20%
Transport to Midwest1 + 0.2 cents/kg
Transport to Asian markets2 + 0.2 cents/kg
1 – Fort Saskatchewan to Chicago, 10 car lots vs. Houston to Chicago, same basis.
2 – Fort Saskatchewan to Hong Kong in 5000 ton lot vs. Houston to Hong Kong, same basis.
Reference: Alberta’s Petrochemicals – Transportation Assessment – Alberta Department of Economic Development Updated to January 1999.
Labor costs in Alberta are slightly below the USGC for plant operating, and construction costs are generally utility costs are
lower.
The transportation factors are slightly negative for the continental markets against the USGC, but in the Pacific Rim markets, an
Alberta plant would have favorable shipping costs and a good response time. Shipping time from the Gulf Coast to Asian through
the Panama Canal takes 30 to 39 days, while out of the BC ports 15 days is shaved off the delivery typically.
From a market point of view, a new facility in Alberta should be in a position to back-out some of the $70 million or so imports
of AA and esters from Japan moving into the U.S. market. In addition, a portion of the $40 million of U.S. imports into Canada
should be open to a new plant.
6.5 Phenol
A product with strong regional potential in Alberta is phenol. However, the major drawback at this point, in time, is a lack of
benzene for making the chemical either through the cumene route or through a new more direct benzene reaction. It is being
included as an adjunct possibility for Alberta’s use of propylene.
While there has been a reasonably strong expansion of the North American capacity carried out or planned in the past year or
two, technology is also having an impact on the business. A new process that does not generate acetone as a coproduct or
byproduct is being refined in a full production plant.
Phenol must be considered as a commodity petrochemical. While small amounts of the product go into the specialty chemicals
and formulated chemicals sectors, which are the focus of this study, the bulk of use lies outside of these areas.
The market growth in the U.S. has been driven by the growth in three major plastic resins – epoxy, nylon and polycarbonate
resins. Bis-phenol A is used for making epoxy resins and polycarbonates, as well as other chemicals. These two resins are
undergoing strong growth at present. Polycarbonate is being driven by its use in glazing as well as in compact discs, while epoxy
resins are finding greater use in industrial and consumer applications as adhesives, coatings and casting compounds.
Other demand areas for phenol lie in the wood binder business where phenolic resins dominate for outdoor grades of plywood,
oriented strand board, and increasingly manufactured studs and beams.
In Canada, demand for phenol is supplied by imports, and the bulk of supply comes from the U.S. The share of the market held
by U.S. producers has remained fairly constant over the years in part because of the spread-out nature of the domestic market.
Major demand lies in Ontario, Quebec and the Maritimes, but it is also scattered into Alberta and BC.
With no bis-phenol A production or caprolactum demand in Canada the bulk of the imports goes into the phenol resins business,
which has been growing at 4 to 5% annually.
Regional Market
The major regional market for a phenol plant located in Alberta lies in the phenolic resins area. Major multi-plant producers in
the region are Borden Chemical, Neste Resins and Unibord Inc. with Georgia Pacific having several plants along the U.S. East
Coast, as well.
In addition to the regional market for phenol in the wood adhesives business, Arisitech has a bis-phenol A plant associated with
its phenol operation at Haverhill, OH. Allied-Signal has a caprolactum facility at Hopewell, VA for its nylon business.
These plants have been serving the plywood and oriented strand board (OSB) plants in Eastern Canada and along the Atlantic
coast. With the changes in board technology coupled with a strong construction sector demand for phenolic resins has been
booming. Several new and large wood board plants have come on stream in the past three years within the region increasing
demand for wood binders.
Demand growth is likely to continue for phenolic resins and phenol in Canada. The wood board industry has developed synthetic
lumber products – stud and beams – using wood chips bound together with phenolic resin. By allowing the wood industry to use
smaller trees and what used to be waste wood to make dimensional lumber and semi-finished products demand is increasing.
Regional supply of phenol consists of four world-scale plants with a total capacity of 1,332-kty (2,930 million pounds per year).
The Blue Island facility of JLM Industries could also be considered part of the regional supply. Sun’s Philadelphia plant and
Aristech’s Haverhill, OH facility are both being expanded, and each will come up to over 630-kty (1,385 million pounds per
year) of capacity. These two expansions will add a total of 545-kty (1,188 million pounds per year) of capacity to the regional
market.
Consolidation has been occurring in the phenol business. The most recent shift saw Sun Chemical buy Allied-Signal’s phenol
business, which tied phenol production to Sun’s cumene capacity in the Philadelphia area. Also, relationships are firming up.
Solutia’s new plant in Florida will have JLM Industries as a partner to take a portion of the output.
Over the past year, the phenol industry has announced expansions that will more than double North American output, if all the
plants are constructed. To this point, the ‘brown-field’ expansions have been going ahead strongly with Sun bringing on stream
the Allied Signal expansion after its acquisition of the Allied facilities.
The phenol business requires access to cumene on a favorable geographic and business basis. Several of the phenol producers are
integrated backwards. Shell, JLM Industries, Texaco, and Georgia Gulf are all cumene producers. The Dow Chemicals plant in
Freeport, TX buys cumene on a merchant basis, but the company can draw upon its European cumene supply should local pricing
dictate an advantage to importing product.
In the production of phenol for each tonne of product made 0.6-tonnes of acetone is generated.
From a production technology, point of view, the phenol process fits extremely well for the production of bis-phenol A, which
requires 0.9-tonnes of phenol and 0.3-tonnes of acetone to produce a tonne of product. Generally, however, the acetone markets
have been smaller than the phenol markets, so finding homes for acetone has occasionally been a problem.
Over the years, several developments have resulted in processes that do not generate acetone in the production of phenol.
Kalama Chemicals in Kalama, WA generates phenol by the oxidation of toluene with benzoic acid as an intermediate. That
process was at one time also used by Chatterton Chemicals in Vancouver, BC (now closed).
There is a growing move to processes that do not produce acetone. Kalama’s route, which was developed by Dow Chemical, is
the pioneer in the area. Today Merichem in Houston, TX and Dakota Gasification in Beulah, ND, also use processes that only
produce phenol (total non-phenol capacity is 65-ktonnes per year or 143 million pounds per year).
The major move in the direction of acetone, less production of phenol is the recently announced 136-kty (300 million pounds per
year) plant that Solutia is building in Pensacola, FL. Solutia holds the rights outside of Russia for technology developed by the
Boreskov Institute of Catalysis. This process starts with benzene and does not require cumene to move through to a phenol
output.
Solutia’s Russian process uses nitrous oxide, either from its adipic acid production or from ammonia at the Florida plant site as
well as the two raw materials. Costs are reported to be 20% lower than the traditional route.
Capital costs on phenol plants vary, but in petrochemical terms, they are not expensive. A recent 136-ktonnes per year (300
million pounds per year) plant in Singapore is budgeted at $128 million Canadian ($85 million U.S.). Even the new Solutia plant
in Florida is likely under $150 million Canadian ($100 million U.S.), since JLM Industries is only paying $54 million Canadian
($35 million U.S.) towards capital costs for just under half the output.
Today margins on the products are good with pricing in the $1.35 Canadian per kilogram (41 cents U.S. per pound) level and
cumene selling at 63 cents Canadian per kilogram (19 cents U.S. per pound). The present, round of plant expansions have been
predicated on this type of price spread. However, the new plant investments are expected to drive down pricing in the next few
years. The over supply is expected to bring margins down to a level of 10 to 15% or less.
In the short and medium-term, the potential for attracting a ‘player’ to Alberta may be modest. The phenol business is undergoing
a 55% increase in capacity at this point, in time and running through to the year 2000.
Secondly, much of the phenol industry in North America will wait on new investment to see how the Solutia plant in Florida
operates. The process claims to have low costs by removing the cumene production step in the route to phenol. While many of
the phenol producers also have strong market position in acetone, the new technology may make any new investor cautious about
a new plant in the short term, given the potential for competitive economics to shift downward.
Preliminary
• The 280-kty availability figure is possibly conservative, but it is very subject to the success of current/future
contract negotiations. (Another 100 or so kty may become available, conversely, 90-kty may not.)
All or Nothing
• Byproduct supply will be an all or nothing affair from all sources, except possibly for ethylene production
byproduct propylene and there, only if sufficient rail cars remain available to move excess raw propylene to the
USGC. (With several hundred cars involved without its local processing this is a big ‘if’.)
Purification Capacity
• The purification facility will be receiving at a rate of up to 330-kty of propylene on occasion – e.g., no shutdowns,
slightly above design production rates at most suppliers, and down to less than 180-kty during shutdowns. The
processing facility must have a 300-kty capacity with up to turndown capability, unless railcars kept are available
to move long-term excesses south. (Major raw propylene storage is essential in any byproduct propylene-
processing scheme.)
Only the oil sands propylene is expected to be received by pipeline, with significant railcar movement for ethylene plant and
refinery material.
The various feeds will carry a variety of impurities – e.g., methyl acetylene propadiene (MAPD) at 3 to 5% in ethylene plant
feeds, but at 100-ppm or less in other feeds, sulphur compounds, and possibly arsenic, phosphorus, mercury and other metallic
compounds.
Ethylene P
MAPD
Plant Feeds Treatment Distillation
Hydrogenation
P
R* To New AIH or SIA Area
C2’s to Fuel Propylene Users
R
P To Other Propylene Users
Other Feeds
R Feed C4 + C3 Product
Caverns Byproducts Propylene
Caverns P - Pipeline
R - Rail (plus truck?)
Extensive raw feed storage is essential, up to one million barrels (1150,000-m3). Ethylene plant high MAPD content
must be reduced and depending upon byproduct propane and butanes plus specifications likely a final hydrogenation
will be needed. Other treating can be perhaps before or after the final propylene purification distillation.
This study assumed byproduct purification to a polymer (99.5%) grade product as the only significant difference
between chemical (94 to 95%) and PG is the size and type of distillation equipment. We believe a prudent processor
would design for PG to suit PP plant needs, although the other short-listed propylene derivatives require only a
chemical grade. (There will be some economic advantages if they use PG, but possibly not enough to warrant a PG
price.)
Hydrogen (Optional)
Existing
Propane Propylene Consumer
Systems
P
C3 Dehydrogenation
Propylene Cavern
Cavern
Storage Feed C4’s
P - Pipeline
6
Propane is also being used as a feed to acrylonitrile in a new Asian plant in lieu of propylene.
7
Areas of high capital costs and high propylene derivative transport charges.
7.3.4 Sizing
• This study assumed a 350-kty (of propylene) facility due to that size being a relatively standard single train facility
(and good cost data being available).
• At that size roughly 14,000-BPD (2,150-m3) of commercial propane would be needed (similar to AEF field butane
supply rate).
• This size could carry two of the short-listed chemicals, assuming each at minimum size.
Ethylene Plant
• Raw propylene now goes to USGC with very roughly 3.5 to 4.0 cents U.S. per pound freight cost.
• Current Gulf Coast processing to PG product cost is estimated very roughly in the order of 7 to 10 cents U.S. per
pound.
Oil Refineries
• Refineries must make up for reduced gasoline production via blending stock or finished gasoline purchase or
added crude processing.
• Raw propylene value will vary greatly refinery to refinery greatly being influenced by expansion and/or other
changes needed for different crudes and/or product quality change environmental regulations driver.
Oil Sands
• Propylene will be replaced by natural gas in fuel gas systems – on balance by gas moving north on the
TransCanada system.
• The byproduct aggregator will have quite different negotiations with each source.
• To these replacement/replacement values must be added transport to the byproduct propylene processing center, as
well as processing costs.
8
Roughly half that appropriate for a byproduct propylene route.
Product costs should all be 1 to 4 cents per pound under USGC prices, with marginally lower transport costs to the Pacific Rim
and perhaps marginally higher costs to mid continent markets.
Watching Briefs
• PO and derivatives are complicated by cofeeds, e.g., benzene, and major coproducts such as styrene monomer, but
PO is not to be forgotten.
• Phenol, but benzene supply much more critical than propylene, has significant lower demands, the only example
noted in this study.
Other Chemicals
• This study did not show much encouragement for n-butanol, 2-EH and isopropanol as markets are not expanding
at any significant rate. (While 2-EH has some local market as the nitrate salt as a cetane improver in oil sand
derived diesels; this market may not last and is now well supplied with low cost Asian supply.) However, one
very knowledgeable contact indicated he felt oxo chemicals would eventually be produced here with CO and
hydrogen available from hydrogen and methanol production units.
7.3.7 Companies
• Throughout the analysis, certain chemical company names arose several times, often relative to their own core
product/market interests. Dow, Shell Chemical, BP Amoco, Degussa for example, are already very active in
Alberta. BASF, Huntsman, Solutia were also noted several times and may be enticed here. This is but a starter
list of companies with core propylene derivative interests. Such companies will decide which propylene (and
related feed) derivatives, if any, are important to them in an Alberta content.
• Availability of cofeeds such as benzene for a styrene/PO facility and/or phenol will be important to many
companies.
• Utility et al Availability – many ‘newcomers’ will be assuming over-the-fence availability of oxygen, nitrogen,
hydrogen, CO, steam, electricity and even plant air as is now almost standard in Europe and on the USGC.
• Low construction costs should prove attractive.
Note: Note that Alberta sites will be compared with Asian, U.S. and possibly European sites where more or less government
financial support is available – e.g., a current largely government funded Netherlands to Ruhr Valley propylene
pipeline. (Such assistance at competitive sites has not been considered in this study, but we believe it is an important
decision factor, especially to companies not already located in Alberta.
Propylene Pricing
• Pricing in the order of two cents U.S. per pound of PG propylene, below USGC on average for byproduct
propylene, assuming grassroots facility – with integration at existing facilities cost could well be less.
7.5 Recommendations