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Correlation of scraped’-film heat transfer in the votator

A. H. P. SKELLAND
Research & Development Laboratories, Thomas Hedley & Co., Limited, Newcastle-upon-Tyne

(Received 29 May 1957)

Abstract-This work on a votator was undertaken to correlate the scraped. film coefficient of
heat transfer, h,, with operating conditions, plant dimensions and physical properties of the fluid.
‘4 All the available data, which include runs on the cooling of glycerol, water and two similar
glyceride oils in four votator-assemblies, are provisionally correlated by the dimensionless

The ratio of shaft to tube diameter, D,/Dt, varied little throughout the work, from 0.75 to
091, so that any effect of this ratio is included in the constant of 4.9.
There is some indication however, of the existence of flow regimes analogous to streamline,
transitional and turbulent conditions in flow through conduits and in conventional liquid mixing
operations. This evidence indicates that exponents on the groups D,N/v and Dtv p/p are
higher in the turbulent range than the values appearing in the above equation.

R6zum&--Ce travail sur un “ votator,” a et6 entrepris dans le but de relier le coefficient
d%ehange de chaleur a travers le film balaye, h,, aux conditions operatoims, propri&s physiques
du fluide et caracteristiques de l’appareil. Toutes les donnes, disponibles, comprenant des essais
le refroidissement du glycerol, de l’eau et de deux glycerides homologues dans quarte assemblages
de votators, satisfont a la relation sans dimension suivante :

Le rapport de l’arbre au diam&re du tube D,/D, a pm vari6 au corns de ces travaux (de 0,75
B O,Sl), de telle sorte que la constante 4,9 suffit a rendre compte du phenomene pour cette falble
variation.
11 existe cependant quelques indications sur les regimes d’&oulement analogues aux r&imes
laminaiis transit&es et turbulents dans les conduites et dans lea operations de melange.
Ces remarques montrent que les exposants des groupes D&V/v et Dfu p/p sont plus grands en
r&ime turbulent que les valeurs mentionnees dams l’equation precit6e.

Zusammenfassung-Diese Untersuchung an einem Votator wurde untemommen, um die


W&rmeilbergangszahl beim Abstreifen, h,, mit den Arbeitsbedingungen, den Abmessungen der
Anlage unde den physikalishchen Eigenschaften der Flilssigkeit in Beziehung zu setzen. Alle
verfiigbaren Daten, in denen Versuche iiber die Kilhhmg mit Glyzerin, Wasser und zwei &r&hen
Glyzeri&len invier Votatoranordnungen enthalten sind, kijnnen vorliiuflg durch folgende dimen-
sionslose Beziehung dargestellt werden.

Das Verh&ltnis von S&aft - zu Rohrdurcbmesser (D,/DJ gndert sich nur wenlg innerbalb
dieser Untersuchungen, nZimlich von 0,76 his 0,81, so dam ein etwaiger Einfluss dleses Quotienten
in der Konstaten 4,9 enthalten ist.
Es gibt einige Anzeichen fur die Existenz von Sttimuirgsbereichen iihnlich der laminaren,
ubergangs - und turbulenten Form bei der Kanalatrijmung oder den iiblichen Mischverfahren
von Fliissingkeiten. Im turbulenten Bereich sind n&m&h die Exponenten der Kenngriissen
DIN/v und D#v p/p hijher als sie in der obiien Gleichung erscheinen.

166
Correlation of scraped-8lm heat transfer in the votator

Attached to each shaft and 180” apart were two scraper


blades of the “ floating ” type, which moved freely to the
THE Votator, a double-pipe, scraped surface wall under centrifugal force and fluid kinetic pressure as
heat exchanger, is widely used in the food and the shaft revolved. (The shaft plus blades is called the
chemical industries, for example in the crystalliz- mutator).
ing of petroleum waxes, the plasticizing of mar- The votator tubes were made of mild steel with thinly
chromium plated inner surfaces. .
garine and shortenings and in- sulphation and
sulphonation reactions.
Materials used and their physical properties
Despite its widespread applications, only one
Water and glycerol. Since the glycerol contained a small
paper has been found dealing quantitatively with
but unknown quantity of water its viscosity was measured
heat transfer in the votator. This paper, by in a Ferranti viscometer ; the results are shown in Fig. 8.
HOULTON [6], deals with a water-to-water heat For the other physical properties those for pure glycerol
exchange in a small laboratory unit, in which were used. Two similar glyceride oils, A and B, were C&o
used and the following typical values were taken for their
shaft speed, jacket water velocity and throughput
physical properties :
rates were studied in relation to the over-all and
film heat transfer coefficients. Specific heat : (partially crystalline oil beyond
No correlation of the scraped film coefficient of votator) 0.45 B.t.u./lb “F
heat transfer with operating conditions and Specific heat : (less crystalline oil within votator)
physical properties has previously appeared, 0.5 B.t.u./lb “F [3]
although the need for such a correlation was Latent heat of fusion : 95 B.t.u./lb.
underlined thirteen years ago by HOULTON, Thermal conductivity : 0.1 B.t.u./hr ft2 “F/ft [3]
whose data is used in the present work. Specific gravity : 0.89.
Many of the present data were obtained
incidentally during work on a more extensive F’rJgressive crystallizing of the oils along the votator,
plus substantial super-cooling, prevented accurate assess-
investigation, If the study of heat transfer
ment of an average viscosity within the device.
through the scraped film had been the prime Values in Fig. 9 for similar oils at temperatures above
object of that work, cooling would have been cloud point [O] were extrapolated through about 20°F to
effected by brine rather than by direct-contact pravide values within the relevant temperature range.
ammonia evaporation, thus simplifying measure- A reason for accepting this procedure is given later.
The equilibrium percentage solid content at a given
ment of the heat transferred. In an ideal case
temper&me was estimated experimentally as “ Solid
also the fluids on the scraped surface side would Content Index” (S.C.I.) using the method and termin-
have been chosen to avoid phase change. ology of FULTON, LUTTON and WILLE [a].
Measurements were as follows :

EXPERIMENTAL WORK Table 2


Apparatus
Two ammonia-cooled votators were used, they were
structually similar and the small unit is shown in Fig. I.
They were designed by the GirdIer Corporation (U.S.A.)
and made by A. Johnson & Co. (London) Ltd., the details
being as follows
Table 1
Small Linear interpolation has been found to give a good
Votator laboratory Large unit approximation between these temperatures for these
Pcnit oils [9].
No. of tubes in series 1 2 or3
“ Effective ” scraped area, AO(fta) 0.687 7.99 11-0s Determination of the eqerimental scrapedfilm coefficients
Heat transfer tube o.d. (in.) 3.25 4.375 4.375 Experimental conditions and results from runs on the
Heat transfer tube i.d. (in.) 3.00 4.00 4.00 small votator appear in Table 8, values calculated from
Revolving shaft o.d. (in.) 2.25 3.25 3.25 HOULTON’B runs are given in Table 4, while values ob-
A. Johnson & Co. specification no, 3/4IA M123A
tained on the large votator are given in Table 5.

167
~o

II
. ~ ~ ~ @ ~ @ ~ ~ ~ @ ~ ~ ,

~tt %

It_t~

..~ ..~ .~

168
Correlation of scraped-film heat transfer in the rotator

~J
A

i!

169
A. H. P. SKELLANIJ

Ammonia Ammonia fihn coefficients were therefore calculated


from a correlation by MCNELLY [v], based on a nucleate
boiling mechanism. The properties of the ammonia film
were evaluated at the mean film temperature. If either
the bulk temperature or the adjacent metal wall tem-
perature had been used the resulting film coefficients
would have differed from that corresponding to the mean
film temperature by less than 2 per cent, which is well
within the limits ,of accuracy of MCNELLY’S correlation.
Scraped film coefficients were than extracted from the
overall coefficients by the.general equation :

1
-=‘+f+$
outiat u h= m ,
I%. 1. Longitudinal and cross-sectional diagrams of
Here h,,, is the usual metal wall coefficient, given by
ammonia-jacketed laboratory votator.
dividing the thermal conductivity by the metal thickness.

Over-all coefficients based on the inside scraped surface DIMENSIONAL ANALYSIS


area of the votator were first calculated from the general
Heat transfer through the scraped fdm will be
equation :
Q = UA> L.M.T.D. by conduction and hence the thermal con-
ductivity, k, of the fluid is involved. The fYm
where the “effective” scraped area, A,, was calculated
thickness should depend on the linear axial
in accordance with HOULTON’S assumption [s] that the
flanged heads of the refrigerant jacket were only half velocity, v, of the fluid, on fluid density, p,
effective for cooling. viscosity, CL,tube diameter, D,, mutator shaft
In the case. of the glyceride oils A and B, the heat speed, M, shaft diameter, D,, and upon the
transferred per hour Q, consists of :- diameter of the mutator, D,, which last is defined
Heat equivalent to about 85 per cent of the energy as twice the distance from the blade edge to the
consumed by the mutator motor [9]. shaft axis. In view of the phase-change of some of
Sensible heat due to cooling the partially crystall- the oil, and the possibility of modifications in
ized oil.
flow pattern along the freezer, the tube length, l#,
Latent heat resulting from some crystallization of
and blade length l,, may be influential factors.
the oil in the votator.
Also, for a given rate of heat transfer, the bulk
tie fraction crystallizing in the device was calculated
temperature of the stream is affected by the
as the difference between the S.C.I. at the maximum
temperature reached by the partially solidifying oil after
specific heat of the fluid, cP, which must also be
emerging from the votator and the crystallization cor- included.
responding to the temperature. rise beyond the votator. The dimensions chosen as fundamental in the
Allowance was made for frictional and mechanical h&at analysis were mass, length, time, heat and
effects beyond the votator from preliminary heat balance
temperature, necessitating the inclusion of the
measurements.
Attempts to calculate the ammonia film coefficient
mechanical equivalent of heat, J - a dimensional
either by assuming a forced convection mechanism and constant. Thus the general equation relating h,
using the usual Dittus-Boelter equation, or by assuming a to these twelve factors in exponential form and
natural convection mechanism and using the usual where I$is a constant is :
correlation involving Nusselt, Grashof and Prandtl
numbers, led to an ammonia film coefficient less than the h, = +(D; 0,” D:Zbd2~~vgc~kjpn/1PJq) (1)
overall coefficient-an impossible result.
It was thus concluded that a much higher ammonia
Dimensional analysis of this relationship leads
film coefficient resulting from a nucleate boiling mechanism
must be prevailing. This was partly confirmed by visual
to the general equation :
observations of vapour plus entrained liquid ammonia
flowing upwards past a glass window in the upper outlet
pipe from the ammonia jacket.
*
Correlationof scraljed-ti heat transferin the votatm

lb almost equals It, equals L (say), r equals d + e, DLP


.
vs

q was found to be zero and the assumption has been


P
made that D,,JDt is unity, a point commented on
where cp p/k remained constant for each curve,
later.
and DJD, and L/D, remained constant through-
The Nusselt and Prandtl groups have their
out.
usual significance, while the group D,v p/p only
The slope of Fig. 3 shows n td be about 0.52 ;
resembles the Reynolds number since it contains
this value was slightly revized later from a final
the tube diameter, 13,, instead of the equivalent
plot pf all the available data.
diameter of the annulus between tube and mutator
shaft. The group Da/v is the ratio of a measure
of the rotary pehpheral velocity to axial velocity
of the fluid and the groups D,/Dl and L/Dt
partly define the geometry of the votator.

Powers of the dimensionless groups and the


coefftimt tj3
Physical properties have been evaluated at 1001 I I
average bulk fluid temperatures : 10 100
D&J
Exponentf was evaluated by using the data for P

oil A and glycerol in log - log plots of h,DJk VS. FIG. 3.

w/v.
Here D;o p/p remained constant for each curve,
cp p/k remained constant for each substance, and
Ds/Dt and L/4 remained constant throughout.
The slope of Fig. 2 shows f to be about 0.17.
The significance of the line for water is discussed
later.
1ooc

1000 10000
%, otvp
CL
FIG. 4.

Exponent r. Data for oil A on the small


votator were used with data for oil B on the large
votator when either two or three tubes in series
1C
1 were used. This provided a range of tube lengths
L-z 100
from 0.87 to 11.44 ft. Log-log plots were made of
ho. 2.

Exponent n. In a preliiy assessment of


this exponent, data for glycerol and oil A were assuming the same cp p/k for these two similar
used in-log - log plots of OilS. _

,
171
A. H. P. SICEXJAND

The ratio D,/Dt was no longer strictly constant,


but the variation is considered small, i.e. for the y (q.1’ (c#+r ($4, vs. y
small votator, 13,/o, was 075, while for the
large unit it was 0231. The intercept has a value of 4.9 and the slope of
The slope of Fig. 5 shows r to be about - 0.87. the line gives a revized value for 12of 047.
Expuwnt i. For glycerol, oils A and B and
water, log -log plots were made of ‘ooo)

A value of 047 was provisionally taken for i


from the slope of the line in Fig. 6.
Eqment b. The effects of varying the ratio
D,/ot were not studied and it remained nearly
constant throughout both this work and that of
HOULTON. The factor (D,/DJb is therefore
included in the value of the coefficient found
below.
Coe@k9zt I$ and revised value fm exponent n.
Because of the wide range of values of D;o p/p
covered in this work a final plot of all the data
against this group was made to assess the co-
efficient 4. Fig. 7 shows a log - log plot of : FIG. 5. &

lOO(

Slope=c.a.0*47

/’ 0
0
Glycerol. small vntator
Oil A. small votator

,f/X’
A 0 Oil B. large votator. (2 tubes)_
+ Oil B. large votator . @tubes)
X Water. small votator
X Water. (from Houlton)

Flo. 6.
lo

%
-L
1 loo0

172
Correlation of scraped-film heat transfer in the votator

The equation relating to the line on Fig. 7, would indicate that turbulence is only fully
which contains all the available data, is :- developed in the case of the water runs.

h Dt
-&= Table 6. Ma&mum and minimum values of
k
Pt - WV P/P andD,iWp/t.l
4.9
Fluid tot - 08) ” P/P %,=N P/P
The equation has been determined for values of
D,/Dt between 0.75 and O-81. Min. Mm.

Evidence for the existence of streamline and Glycerol 44.0 175.0


Oil A
turbulent jlow regimes 134.0 f37p.0
Oil B 1690-O 2030.0
It is well known that the transition between Water 28200.0 380,000-O
streamline and turbulent fluid flow through
straight conduits is characterized by values of
D,v p/p between 2000 and 4000, while the There is also some indication of the existence
corresponding transition region for conventional of two regimes of flow in Fig. 2, where the middle
liquid mixing vessels is defined by values of four values for water from Table 4 are plotted to
D,‘N p/p between 10 and 10,000 [5]. indicate an exponent of the order of O-5 for the
Maximum and minimum values of these two group D&/v in the turbulent region. This
forms of Reynolds number are shown for these exponent cannot be determined with greater
runs in Table 6, where the equivalent diameter precision from the available data (that of
of the annulus between tube and mutator shaft, HOULTON) since, although the values of L/D,,
D,, is given by Dt - D, and where the impeller 0,/D* and cP p/k corresponding to points on this
diameter, Di, is taken as D,. From this table line remained constant, values of D, v p/p
analogy with conventional liquid mixing vessels ranged from 5910 to 6350.
.

Slope ~0.57
d= 4-Q

Glycerolmnall votdor
Oil A.small votator I
Oil 8, large votator, (2 tubes)
Oil B, large votdor, (3 tubes)
Water, small wtator
Water (from Houlton) l-

1000 low0

178
A. El. P. SrmILAND

Fig. 4 suggests an exponent of the order of 0.9 perature difference between ammonia and the
for the group L+v p/p in the turbulent region. votated fluid was used ; this practice is only valid
Although the groups L/D,, D,/Dl and cr p/k are if constant specific heat can be assumed as in the
constant for Fig. 4 more data are clearly needed case of water and glycerol. It is believed that this
to establish this exponent under turbulent assumption can be largely justified in the case of
conditions. Analogy with correlations for stream- oils A and B despite their partial phase change
line and turbulent flow through conduits indicates within the votator, in view of their substantially
that the exponent on the group L/D, will at least linear relationship between equilibrium solid
bc reduced for turbulent conditions, due to content and temperature. Thus, over most of
reduced entrance effe&s. the temperature range through which the oil is
It seems from the above observations that the cooled, it has an effective specific heat com-
exponent on the Prandtl group in equation (8) pounded of nearly constant amounts of latent
may be a hybrid value obtained by combining and sensible heat.
data for streamline and turbulent flow. Accord-
ingly the correlation must be regarded as Physical properties of oila A and B
provisional pending further data on the existence A perfect correlation in Pig. 7 is partly prevented
of more than one flow regime and on the various by the shortage of accurate physical data for
group-exponents at high Reynolds numbers. oils A and B, necessitating extrapolations and
It appears, then, that the situation regarding the use of typical values.
equation (8) may resembIe that underlined by In particular, since the true viscosities for oils
comments of PRATT [s] when comparing his A and B at sub-cloud-point temperatures are
own correlation with that of CHILTON, DREW not known, it may be felt that the data for these
and JEBENS [Q] for heat transfer in agitated substances lie on the general line of Pig. 7 by a
vessels. PRAY&S comments strongly suggest that coincidence connected with the use of “ pseudo ”
the well known single-line correlation of CHILTON, viscosities derived from the extrapolation of
DREW and JEBEN~actually spans more than one Fig. 9. However, it should be noted that ex-
flow regime. Comments relevant to this latter ponents on groups containing viscosity (namely
topic also appear in discussions of BROWN, D;u p/p and cp p/k) have not been derived ex-
SCOTTand TOYNE [l]. clusively from data for oils A and B, but have
Features of equation (8). The constants in the been obtained independently from data for
correlation have been found from experiments in glycerol in the case of Dp p/r (Fig. 8) and from
which the fluid was being cooled. The fluid adjacent data for glycerol and water in the case of cp p/k
to the scraped metal wall would thus be colder (Fig. 6) ; true viscosities for glycerol and water
and more viscous than in the main steam. are, of course, known.
Slightly different constants might be expected Furthermore, partial cancellation in the groups
if the fluid were being heated, since the tem- D,v p/p and cp p/k leaves viscosity to the rather
perature gradient and hence the viscosity pattern low power of - 0.1 which may partially account
would be reversed. for the close agreement of data for oils A and B
A eomparison between the exponents on the with the provisional correlation, despite the use
groups D$/v and D;o p/p indicates that the of “ pseudo ” viscosities in place of true values
rate of heat transfer is not dominated by the for these substances.
mutator speed and that the contribution afforded
by linear flow velocity through the votator must Contact between blades and tube wall
be considerable. It is known that even slight clearance between
the edges of the scraper blades and the tube wall
Logarithmic mean temgwrature difference may lead to considerable reductions in heat
In calculating over-all coefficients from the transfer [Q]. Because of the “ floating ” blades
experimental data the logarithmic mean tem- used in this work the assumption has been made
Carehxtion of scrrrped-fUmheat trsnsf’er in the votator

that close contact between blade-edges and wall Acknoroledge me&.9-Useful comment was given
is maintained; this should be true at least for by Mr. L. H. FROOB~S, and the author is grateful
water and glycerol, and by taking D,,JDt equal to Mr. H. R. GALLEYMORE, Director of the
to unity throughout the assumption has been Chemical Division of Thomas Hedley & Co. Ltd.,
extended to the partially crystallizing oils A for permission to publish this paper.
and B.
NOMENCLATURE
Factors
notimluded h the correlation AC = “Effective” scrapedheat transfer surfacefts
The effects of variation in mutator design have % = Specificheat B.t.u/lb”F
not been included, for instance with regard to De = Conduit inner diameter, or equivalent
diameter of an annulus ft
the shape of the cross-section of the shaft, the
Di = Impeller diameter ft
variation of the ratio’ D,/Dt, the number of blades, Dm = Mutator diameter (2 x distance from
and the clearance between blade-edges and tube blade edge to shaft axis) ft.
wall. More work is needed to incorporate the Da = Diameter of mutator shaft ft
above factors and to distinguish more clearly Dt = Internal diameter of Votator tube ft
h, = Metal wall coefficient of heat transfer
between streamline and turbulent conditions.
B.t.u./ftohPF
hNH, = Ammonia 5lm coefficient of heat transfer
B.t.u./ft%P’F
h, = Scraped illm coefficient of heat tranbfer
B.t.u./ft%?F
k = Thermal conductivity B.t.u./ft%r=‘F/ft
lb = Length of scraper blade ( = L) ft
Zr = Length of votator tube ( = L) ft
L.M.T.D. = Log, mean temperature difference
between fluid being cooled and refrigerantOF
N = Mutator shaft speed rev/hr
Q = Total heat transferred/unit time B.t.u./hr
U = Over-all coefficient of heat transfer
B.t.u./ftohPF
u = Average axial flow velocity of fluid
through votator ft/hr
p = Fluid density lb@
p = Absolute fluid viscosity lb/R hr
4 = A proportionality constant -
18
1 Exponents :-
Ai- TDR a, b, c, 4 e, f, g, 6 j, n, P, q.
FIG. 8. Fxo. 9. r=d+e.

REFERENCES
BncwwR. W., Scan R. and TOYNE C. Trans. In&n. Chem. Engm. 1947 25 186,199.
CBILTON T. I-I., Dnuw T. B. and JE~IENSR. H. In&&r. En@@. Chem. (Zndnstr.) 1944 36 510.
ECKEY E. W. Vegetabk Fa& and Oik p.99. Reinhold Pub. Corp., New York, 1954.
FULT~N N. D., Lurro~ E. S. and WILLIER. L. J. Amer. Oil Chem. Sot. 1954 3198.
GREEN S. J. Trans. Ins&a.Chem. Engra. 19.58 31827.
HOWLTON H. G. In&&r. Eng,ng. Chem. (Indzcstr.)1944 36 522.
MCNBLLY M. J. J. Imp. Colt. Chum. Egng. Sot. 1958 7 18.
PRATT N. H. Trans. In&n. Chem. Engrs. 1947 25 170.
Unpublished work.

175

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