Académique Documents
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Culture Documents
(First Edition)
AWWA Standard
Ultraviolet
Disinfection Systems
for Drinking Water
SM
Caution Notice: The American National Standards Institute (ANSI) approval date on the front cover of this standard indicates
completion of the ANSI approval process. This American National Standard may be revised or withdrawn at any time. ANSI
procedures require that action be taken to reaffirm, revise, or withdraw this standard no later than five years from the date of
ANSI approval. Purchasers of American National Standards may receive current information on all standards by calling or writ-
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ii
Producer Members
User Members
* Liaison, nonvoting
Alternate
iii
Foreword 4 Requirements
I Introduction.....................................vii 4.1 Required Equipment..........................5
I.A Background......................................vii 4.2 Data to Be Provided by Purchaser......5
I.B History.............................................vii 4.3 Data to Be Provided by the
I.C Acceptance.......................................vii Manufacturer...............................8
II Special Issues...................................viii 4.4 Materials..........................................11
III Use of This Standard.........................ix 4.5 General Design................................11
III.A Purchaser Options and 4.6 Validation........................................14
Alternatives.................................ix
5 Verification
III.B Laying Length...................................ix
5.1 Factory Testing.................................15
III.C Testing..............................................ix
5.2 Installation.......................................16
III.D Modifications to Standard.................ix
5.3 Manuals...........................................17
IV Major Revisions.................................ix
V Comments........................................ix 6 Delivery
6.1 Packaging.........................................18
Standard 6.2 Shipping, Handling, and Storage.....18
1 General 6.3 Notice of Nonconformance..............19
1.1 Scope.................................................1 6.4 Affidavit of Compliance...................19
1.2 Purpose..............................................1
Table
1.3 Application.........................................1
1 Feedwater Quality Data to Be
2 References.........................................2 Provided by Purchaser..................7
3 Definitions........................................2
I. Introduction.
I.A. Background.Ultraviolet (UV) disinfection systems have gained
increased acceptance for use in water treatment plants based on information that UV
disinfection could cost-effectively inactivate Cryptosporidium. In addition, the Long
Term 2 Enhanced Surface Water Treatment Rule (LT2ESWTR) has recognized UV
disinfection as a best available technology for meeting the requirements of the rule.
I.B. History. The need for a standard addressing UV disinfection systems was
recognized by the American Water Works Association (AWWA) in November 2005.
The committee was appointed for the task of standardization and at the first inaugural
meeting in June 2006, a committee was formed to develop a standard. This first edition
was approved by the AWWA Board of Directors on June 10, 2012.
I.C. Acceptance. In May 1985, the US Environmental Protection Agency
(USEPA) entered into a cooperative agreement with a consortium led by NSF
International (NSF) to develop voluntary third-party consensus standards and a
certification program for direct and indirect drinking water additives. Other members of
the original consortium included the Water Research Foundation, (formerly AwwaRF)
and the Conference of State Health and Environmental Managers (COSHEM). The
American Water Works Association and the Association of State Drinking Water
Administrators (ASDWA) joined later.
In the United States, authority to regulate products for use in, or in contact with,
drinking water rests with individual states. Local agencies may choose to impose
requirements more stringent than those required by the state. To evaluate the health
effects of products and drinking water additives from such products, state and local
agencies may use various references, including
1. An advisory program formerly administered by USEPA, Office of Drinking
Water, discontinued on April 7, 1990.
2. Specific policies of the state or local agency.
* American National Standards Institute, 25 West 43rd Street, Fourth Floor, New York, NY 10036.
Persons outside the United States should contact the appropriate authority having jurisdiction.
vii
viii
ix
AWWA Standard
SECTION 1: General
1
Copyright 2012 American Water Works Association. All Rights Reserved.
2 AWWA F110-12
SECTION 2: References
SECTION 3: Definitions
* American National Standards Institute, 25 West 43rd Street, Fourth Floor, New York, NY 10036.
Institute of Electrical and Electronics Engineers, 3 Park Avenue, 17th Floor, New York, NY 10016.
International Society of Automation, 67 Alexander Drive, Research Triangle Park, NC 27709.
International Safety Equipment Association, 1901 North Moore Street, Arlington, VA 22209-1762.
National Electrical Manufacturers Association, 1300 North 17th Street, Suite 1752, Rosslyn, VA 22209.
** NSF International, 789 N. Dixboro Road, Ann Arbor, MI 48105.
specific to the challenge microorganism used during experimental testing and the
validation test conditions for full-scale reactor testing.
33. Required dose: The dose in units of mJ/cm2 needed to achieve the tar-
get log inactivation for the target pathogen. The required dose is specified in the
LT2ESWTR.
34. Supplier: The party that supplies material or services. A supplier may
or may not be the manufacturer.
35. Target log inactivation: For the target pathogen, the specific log inacti-
vation the public water system wants to achieve using UV disinfection.
36. Target pathogen: The microorganism for which a public water system
wants to obtain inactivation credit using UV disinfection.
37. UV intensity sensor: A photosensitive detector used to measure the
intensity at a point within the reactor.
38. UV transmittance: A measure of the fraction of incident light transmit-
ted through a material.
39. Validation: The testing of a reactor to determine its performance under
all operating conditions, including flow, UV transmittance, and lamp power.
40. Validated dose: The dose in units of mJ/cm2 delivered by the reactor as
determined through validation testing. The validated dose is compared with the
required dose to determine log inactivation credit.
41. Validation factor: An uncertainty term that accounts for the bias and
uncertainty associated with validation testing.
SECTION 4: Requirements
4.2.1.1 Process train location. Identify the location of the system in the
plant process train.
4.2.1.2 Unit processes and chemical application points. Describe the
unit processes and chemical application points upstream of the proposed system.
4.2.1.3 Footprint. Describe the available footprint for the system, service
and maintenance areas, and any restrictions that may apply.
4.2.1.4 Piping. Provide connection pipe size and configuration.
4.2.1.5 Storage. Provide description of available storage area and environ-
mental conditions.
4.2.2 Target pathogen, log inactivation, and dose. Purchaser shall identify
the target pathogen, log inactivation level, and corresponding required dose.
4.2.2.1 Target pathogen. The target pathogen shall be Giardia, Crypto-
sporidium, or virus.
4.2.2.2 Log inactivation. The log inactivation level shall range from 0.5
to 4 logs.
4.2.2.3 Dose. The required dose shall be as specified in the LT2ESWTR
or by state-accepted substitute.
4.2.3 Design flow. Purchaser shall provide the maximum, average, and
minimum design flows for the system and for each reactor.
4.2.3.1 Monthly design flows. Monthly design flows may be provided if
they are presented with corresponding monthly water quality data.
4.2.4 Water quality data. Purchaser shall provide available historical
feedwater quality data for parameters shown in Table 1.
4.2.4.1 Presentation. Feedwater quality values shall be presented for
maximum, minimum, and average values if available. Values may be presented for
1st, 5th, 50th, 95th, and 99th percentile values if the water quality dataset is large
enough to do a statistical analysis.
4.2.4.2 Sampling. Sampling of feedwater for UV254 transmittance is rec-
ommended to be performed weekly over a period of one year to determine seasonal
variations in water quality. Seasonal differences in water quality may be provided if
they follow a repeatable, cyclical pattern and can be used in conjunction with design
flows for sizing the system. For large historical datasets, a conservative UV transmit-
tance design value (typically 1st or 5th percentile of the dataset) shall be selected for a
sizing system unless site-specific variations justify selection of a higher or lower UVT
at the design flow rate. For small groundwater systems (i.e., those designed to treat
less than 100 gpm), a minimum of three UVT is recommended in order to establish
a representative design UVT.
4.2.5 Combined fouling and aging factor. Purchaser shall provide the com-
bined fouling and aging factor, taking into account project-specific water quality
conditions, lamp aging, and sleeve-cleaning effectiveness data received from the
vendors and verified by the lamp manufacturer.
4.2.5.1 Calculation. The combined fouling and aging factor shall be cal-
culated by multiplying the fouling factor by the lamp aging factor; it typically
ranges from 0.4 to 0.9.
4.2.6 Head loss. Purchaser shall provide the maximum allowable head
loss across the reactor, flange-to-flange, at maximum design flow for a predeter-
mined number of reactor trains in operation.
4.2.7 Operating pressure. Purchaser shall provide the maximum working
and test pressure for the reactor vessels.
4.2.8 Power supply constraints. Purchaser shall provide power supply con-
straints that may impact selection and sizing of the system, including available
power supply capacity, backup power capacity, and power quality fluctuations.
4.2.9 Number of UV reactors. If applicable, purchaser shall provide the
number of UV reactors needed, including the number of duty and standby trains
to meet capacity requirements of the system.
4.2.10 Type of system. Purchaser shall provide a description of the reactor
components to be considered for the project, including reactor vessel, lamp type,
electronic or electromagnetic ballasts, online automatic cleaning system or off-line
4.5.9.3 Data capture. The instrumentation and control system shall pro-
vide a means by which flow, UV intensity, lamp status, RED, and UVT are cap-
tured by the reactor or the plant control system.
4.5.9.4 Required functions. The following functions shall be prepro-
grammed into the reactor control panel:
1. For UV systems operating under the UV Intensity Setpoint Approach
method, the measured sensor intensity and flow rate shall be displayed.
2. For UV systems operating under the Calculated Dose Approach, the vali-
dated dose shall be displayed.
3. Lamp hours of operation.
4. Controls shall be equipped with routines to sequence, pace, and control
reactor startup and shutdown.
5. Control system shall have at least two levels of alarm capabilities:
a. Level one shall inform the operator of impending or current issues.
b. Level two shall notify the operator of implementation of emergency
actions such as reactor shutdown or valve closure.
6. Alarms shall include off specification, communication failure, component
failure, high temperature, and excessive hours of lamp operation.
4.5.9.5 Reporting. The system shall have available the information neces-
sary to complete the UVDGM and/or state- or province-specified reports includ-
ing off-specification, calibration, and related records, either automatically, in a log
file that can be printed or transmitted, or on a consolidated screen that the operator
can copy for submission.
Sec. 4.6 Validation
4.6.1 General requirements. UV systems shall undergo full-scale, third-
party validation testing in accordance with the current edition of the UVDGM or
a state- or province-accepted substitute.
4.6.1.1 UVDGM checklists. If the UVDGM validation protocol is used,
the UVDGM checklists shall be included.
4.6.1.2 Validation process. The validation process shall be based on the
following:
1. A challenge dosimeter whose dose response behavior has been character-
ized and quantified with a Low-Pressure Collimated Beam Apparatus in accor-
dance with the quality assurance and quality control provisions in the UVDGM.
2. Identification and documentation of the critical components, including
UV sensors, wetted dimensions, lamps, and sleeves.
SECTION 5: Verification
alignment, is free from any undue stress imposed by anchor bolts, and conforms to
manufacturers electrical connection requirements.
5.2.5 Training. Manufacturer or supplier shall provide training to pur-
chasers maintenance and operating staff.
5.2.5.1 Classroom and hands-on training. Training shall consist of both
classroom and hands-on training.
5.2.5.2 Training materials. Manufacturer or supplier shall provide the
required number of training material packages, which may include manuals, com-
pact disks or digital video disks, and programs.
5.2.6 Acceptance test. After training from the supplier, the equipment
shall be operated by the purchasers personnel, for a specified length of time.
5.2.6.1 Tests. Purchaser shall conduct the following tests to demonstrate
equipment performance:
1. Startup and shutdown sequencing.
2. Alarm verifications.
3. Power failure and power restoration sequences.
4. Power usage verification.
5. Response to flow-rate changes.
5.2.6.2 Test Failure. If the system does not operate trouble-free, the
supplier shall make the necessary corrections and rerun the tests.
Sec. 5.3 Manuals
5.3.1 Operation and maintenance (O&M) manuals. O&M manuals shall
include the following items:
1. Component information. Reactor and subcomponent design criteria,
data sheets, shop drawings, parts lists, and diagrams.
2. Contents. Instructions for receiving, storage, installation, startup, shut-
down, routine and normal operations, regulation and control, and emergency con-
ditions.
3. Calibration. Equipment calibration frequency, procedures, and specifi-
cations. Sensor and UV transmittance calibration analyzer frequency and proce-
dure for evaluation of lamp output variability shall be included.
4. Maintenance. Maintenance instructions for removal and replacement
of subcomponents, including lamps, sleeves, ballasts, fuses, cooling fans, filters,
and cleaning mechanisms. Recommended frequencies of maintenance for filters,
monitors, common subcomponents, and lamp sleeve cleaning.
SECTION 6: Delivery