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ANSI/AWWA B405-00
(Revision of ANSI/AWWA B405-94)
AWWA STANDARD
FOR
SODIUM ALUMINATE
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or withdrawn at any time.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 publication. Purchasers of American National Standards may receive current
information on all standards by calling or writing the American National Standards Institute, 11 W. 42nd St., New
York, NY 10036; (212) 642-4900.
All rights reserved. No part of this publication may be reproduced or transmitted in any form or by any
means, electronic or mechanical, including photocopy, recording, or any information or retrieval system,
except in the form of brief excerpts or quotations for review purposes, without the written permission of
the publisher.
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Copyright © 2000 American Water Works Association, All Rights Reserved
Committee Personnel
The AWWA Subcommittee on Sodium Aluminate, which developed this
standard, had the following personnel at the time:
The AWWA Standards Committee on Iron Salts, Aluminum Salts, and Related
Coagulant Aids, which reviewed and approved this standard, had the following
personnel at the time of approval:
Consumer Members
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Producer Members
*Liaison, nonvoting
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All AWWA standards follow the general format indicated subsequently. Some variations from this format may be
found in a particular standard.
Standard 6 Delivery
1.3 Application............................................. 1
I. Introduction.
I.A. Background. Sodium aluminate (Na2Al2O4) is used to improve hardness
reduction and coagulation when softening water with lime or lime and soda ash. It
can also be used in conjunction with alum to improve coagulation.
Sodium aluminate is a manufactured product obtained by combining aluminum
oxide (Al2O3) with sufficient excess causticity for stabilization. Sodium aluminate is
produced either as a solid or liquid. The solid form is a white or brown granular
material containing 60–80 percent Na2Al 2O4 (19.75–26.33 percent aluminum). The
density of solid sodium aluminate is 800 kg/m3 (50 lb/ft3). Liquid sodium aluminate
is a concentrated solution containing approximately 30–45 percent Na2Al 2O4 (9.87–
14.80 percent aluminum). The specific gravity of liquid sodium aluminate is 1.45–1.60.
Refer to material safety data sheets (MSDS) available from the supplier or
manufacturer for safety information.
I.B. History. Prior to May 15, 1960, a tentative standard for sodium
aluminate was designated AWWA B405-59T. On May 15, 1960, the first edition
was approved. Subsequent revisions to AWWA B405 were prepared by the
AWWA Standards Committee on Iron Salts, Aluminum Salts, and Related
Coagulant Aids and approved by the AWWA Board of Directors in 1983, 1989,
and 1994. This edition was approved by the AWWA Board of Directors on J une
11, 2000.
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 all direct and indirect drinking water additives. Other
members of the original consortium included the American Water Works
Association Research Foundation (AWWARF) and the Conference of State Health
and Environmental Managers (COSHEM). The American Water Works Associa-
tion (AWWA) and the Association of State Drinking Water Administrators
(ASDWA) joined later.
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*Persons in Canada, Mexico, and non-North American countries should contact the
appropriate authority having jurisdiction.
†American National Standards Institute, 11 W. 42nd St., New York, NY 10036.
‡NSF International, 789 N. Dixboro Rd., Ann Arbor, MI 48105.
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ANSI/AWWA B405-00
(Revision of ANSI/AWWA B405-94)
SODIUM ALUMINATE
SECTION 1: GENERAL
Sec. 1.1 Scope
This standard describes sodium aluminate (Na2Al 2O4) in both liquid and solid
form for use in water supply service. Sodium aluminate according to this standard is
a combination of sodium oxide (Na2O) and aluminum oxide (Al2O3) with sufficient
excess causticity (sodium oxide) for stabilization.
SECTION 2: REFERENCES
This standard references the following documents. In their latest editions, they
form a part of this standard to the extent specified in this standard. In any case of
conflict, the requirements of this standard shall prevail.
ASTM* E11—Standard Specification for Wire-Cloth Sieves for Testing Purposes.
Standard Methods for the Examination of Water and Wastewater. APHA,†
AWWA, WEF.‡ AWWA, Denver, Colo. (19th ed., 1995).
SECTION 3: DEFINITIONS
The following definitions shall apply in this standard:
1. Liquid sodium aluminate: The liquid form of sodium aluminate is a
concentrated solution containing approximately 30 to 45 percent Na 2Al2O4.
2. Manufacturer: The party that manufactures, fabricates, or produces mate-
rials or products.
3. Purchaser: The person, company, or organization that purchases any
materials or work to be performed.
4. Solid sodium aluminate: The solid form of sodium aluminate defined in
this standard is a white or brown granular material containing 60 to 80 percent
sodium aluminate.
5. Supplier: The party that supplies materials or services. A supplier may or
may not be the manufacturer.
*American Society for Testing and Materials, 100 Barr Harbor Dr., West Conshohocken, PA
19428-2959.
†American Public Health Association, 1015 15th St. N.W., Washington, DC 20005.
‡Water Environment Federation, 601 Wythe St., Alexandria, VA 22314-1994.
SECTION 4: REQUIREMENTS
Sec. 4.1 Physical Requirements*
4.1.1 Form and size. Solid sodium aluminate shall be dry (<25 percent free
water), clean (<1 percent foreign matter), and free of lumps. The solid form shall be
pulverized or granular, as specified. Liquid sodium aluminate shall be sufficiently
stable for prolonged storage of more than approximately 30 days.
4.1.2 Insoluble matter. Solid sodium aluminate shall contain no more than
1.0 percent insoluble matter. Liquid sodium aluminate shall contain no more than
0.5 percent insoluble matter.
*All sieve numbers referred to in this standard are US Standard Sieve Series numbers, as
specified in ASTM E11.
†See Sec. I.C of the foreword.
SECTION 5: VERIFICATION
Sec. 5.1 Sampling
5.1.1 Sampling point. Samples shall be taken at the point of destination.
5.1.2 Amount of shipment to be sampled. Five percent of the packages or
containers shall be sampled, but a minimum of 5 packages and a maximum of 15
packages in any one shipment shall be sampled. No sample shall be taken from a
broken package.
5.1.3 Sampling method, sample size, and handling for solid form.
5.1.3.1 Granular or pulverized sodium aluminate may be sampled by using a
sampling tube at least 3/4 in. (19 mm) in diameter. If the solid sodium aluminate is
handled by conveyer or elevator, a mechanical sampling arrangement may be used.
5.1.3.2 The gross sample shall weigh at least 10 lb (5 kg), and shall be mixed
thoroughly and divided to provide three 1-lb (0.50-kg) samples.
5.1.3.3 The samples shall be sealed in airtight, moistureproof, plastic containers.
5.1.3.4 Each sample shall be labeled for identification and shall be signed by
the sampler. A chain-of-custody form shall accompany all samples and shall be
properly completed by the individuals handling the samples.
5.1.4 Sampling method, sample size, and handling for liquid form.
5.1.4.1 The contents of each container to be sampled shall be mixed thoroughly
by rolling or by other means. A portion shall be taken from each container of such
size that the total gross sample shall consist of at least 10 qt (10 L).
5.1.4.1.1 When collecting a representative composite sample from a tank car or
tank truck, at least five different portions shall be taken. The portions shall be taken
from locations well distributed in depth and area or at timed intervals during
discharge, in order to obtain a representative sample. The five portions making up
the composite sample shall be mixed in a clean, dry plastic container to give the
composite sample at least a 10 qt (10 L) volume.
5.1.4.2 After thorough mixing of the gross sample, three 0.5-qt (0.5-L) samples
shall be sealed in airtight plastic bottles. When sampling, large quantities of air must
not be introduced into the product for this will affect the stability of the aluminate.
5.1.4.3 Each sample container shall be labeled for identification and shall be
signed by the sampler. A chain-of-custody form shall accompany all samples and shall
be properly completed by the individuals handling the samples.
5.1.5 Laboratory examination. Laboratory examination by the purchaser of
one of the three samples collected according to Sec. 5 shall be completed within 10
working days after receipt of the shipment.
5.1.5.1 Test samples. Test samples shall be obtained from sealed material
samples delivered to the laboratory. Material samples shall be unsealed only when it
is necessary to remove quantities of the material for testing. This shall be performed
quickly, and the material samples shall then be resealed for future reference.
5.1.5.2 Retention. Samples shall be retained for at least 30 days after date of
receipt or until the load of sodium aluminate has been completely used, whichever is
longest before they are discarded.
5.1.6 Sample preparation.
5.1.6.1 Solid sodium aluminate. The material sample delivered to the labora-
tory shall be quartered to approximately 3.5 oz (100 g), and this amount shall be
reduced by mechanical grinding or by hand in a mortar to a size that all of it passes
a No. 30 sieve. After thorough mixing, the test portion shall be stored in an airtight
container and weighed out rapidly to avoid a change in moisture content.
5.1.6.2 Liquid sodium aluminate. Liquid sodium aluminate shall be mixed
thoroughly before a portion is withdrawn for examination, and the bottle shall be
kept sealed after the test portion has been removed.
5.2.1.2 Procedure.
1. Dry and accurately weigh (±0.0001g) a piece of 5.5 cm Whatman 934-AH
glass microfiber filter paper.
2. Accurately weigh (±0.0001g) 5 g of sample in a tared beaker. Dissolve the
sample in 150 mL of DI water.
3. Using a vacuum filtration flask, Buchner funnel, and aspirator, filter the
sample.
4. Wash the beaker with 50 mL of DI water and pour the wash water through
the filter. Repeat with two additional washings.
5. Dry the filter paper in an oven at 100–105° C to constant weight. Let cool
in a desiccator.
6. Accurately reweigh the filter paper. This value minus the weight in step 1
is the weight of the undissolved solids.
5.2.1.3 Calculations
NOTE: During the first analysis on a given sample, the filtrate may need to be
tested for hydroxide alkalinity to determine the amount of wash water required to
remove the alkalinity from the residue.
6. Transfer the filtrate (step 5) to a 500-mL volumetric flask, cool to
approximately room temperature, and make up to 500 mL with distilled water.
7. Mix thoroughly, measure 50 mL into a 250-mL beaker and add 75 mL of
hot distilled water.
8. Place the beaker in a boiling-water bath and bubble carbon dioxide
through the solution at the rate of four bubbles per second. Continue bubbling until
precipitation is complete (approximately 30 min).
9. When precipitation is thought to be complete, discontinue bubbling and
allow the precipitate to settle. Remove some of the supernatant liquid and pass
carbon dioxide through it. If no precipitate forms, the alumina has been precipitated
completely. Return the supernatant to the beaker. If preferred, the phenolphthalein
indicator may be added to the solution before gassing begins, and the gassing may be
continued for 20 min after the color of the indicator has disappeared.
10. Filter with suction through two quantitative filter papers (Whatman
No. 42 or equivalent) supported in a platinum cone or glass funnel. Wash thoroughly
and carefully with hot distilled water. Save the filtrate and wash water to determine
the total sodium oxide (Sec. 5.2.4).
11. Dry the paper and residue in a tared platinum crucible and ignite at
1,000°C to constant weight (approximately 1 hr).
12. Cool in a desiccator and weigh quickly to avoid the absorption of moisture.
The weight of the crucible and residue minus the tared weight of the crucible is equal
to the weight of the alumina.
13. From the weight of alumina, subtract the weight of soluble silica
(Sec. 5.2.3) to obtain the net weight of alumina.
5.2.2.3 Calculations.
weight of residue
----------------------------------------------------------------- × 100 = percent soluble SiO 2 (Eq 4)
weight of sample (0.5 g)
5.2.4.3 Calculations.
V4 0.040 g NaOH V 4
V – ------ (V ) – V × ------------------------------------------- × ------ × 100/W = percent NaOH
1 V 3 2 mL 1.0N NaOH V 5
5
Where:
V1 = millilitres, 1.0N H2SO4 = 25 mL (step 2, Sec. 5.2.4.2)
V2 = millilitres, 1.0N NaOH titrant (step 3, Sec. 5.2.4.2)
V3 = millilitres, initial 1.0N NaOH volume = 80 mL (step 1, Sec. 5.2.2.2)
V4 = millilitres, sample aliquot = 50 mL (step 7, Sec. 5.2.2.2)
V5 = millilitres, total sample volume = 500 mL (step 6, Sec. 5.2.2.2)
W = grams, sample weight = 5.0 g (step 1, Sec. 5.2.2.2)
(percent excess NaOH) × 0.7748 = percent excess sodium oxide as Na2 O (Eq 8)
5.2.7.2 Procedure.
1. Make the filtrate obtained from Sec. 5.2.6 up to 500 mL with distilled
water.
2. Transfer 25 mL of the solution to a 250-mL beaker and dilute to about 175 mL.
3. Add approximately 7 mL of concentrated hydrochloric acid. Using a pH
electrode to monitor pH, adjust the solution to pH 7.5 with ammonium hydroxide.
4. Bring the solution to a boil, allow it to settle, and then filter through
quantitative filter paper (Whatman No. 42 or equivalent).
5. Wash with hot 1 percent ammonium nitrate solution.
6. Redissolve the precipitated aluminum hydroxide on the filter paper with a
one-to-one hydrochloric acid solution and wash the precipitate off the paper
alternately with this solution and hot ammonium nitrate.
7. Wash into the original beaker and repeat the precipitation as before.
8. Wash thoroughly with hot ammonium nitrate solution and finally with hot
water until the filtrate is free from chloride. (See the note following step 10.)
9. Dry the filter paper and its contents in an oven at about 100°C and burn
off the paper slowly in a tared crucible.
10. Finally, ignite over a blast lamp for 5 min, weigh quickly, and reignite to
constant weight.
11. Calculate the weight of the residue, which is equal to the weight of the
crucible and the residue minus the tared weight of the crucible.
NOTE: During the first analysis on a given sample, it may be necessary to test
the filtrate for chloride to determine the amount of washing required to ensure that
the filtrate is free from chloride. Refer to Standard Methods for the Examination of
Water and Wastewater of latest revision for determining chloride in water.
5.2.7.3 Calculations.
weight of residue
----------------------------------------------- × 1.608 × 100 = percent sodium aluminate (Eq 9)
weight of sample
5.2.8.2 Procedure.
1. Measure 25 mL of the solution from the 500-mL flask (Sec. 5.2.7) and place
in a 250-mL Erlenmeyer flask.
2. Dilute to approximately 100 mL with distilled water.
3. Titrate with 0.02N sulfuric acid with phenolphthalein as indicator.
5.2.8.3 Calculations.
1L 40 g NaOH V2
V 3 × -------------------------- × C × -------------------------------- × ------ × 100/W = percent NaOH
1, 000 mL 1 mole NaOH V1
percent excess NaOH × 0.7748 = percent excess sodium oxide as Na 2 O (Eq 12)
Where:
C1 = normality of H2SO4 = 0.02N (Sec. 5.2.8.1)
V1 = millilitre, sample aliquot volume = 25 mL (step 1, Sec. 5.2.8.2)
V2 = millilitre, total sample volume = 500 mL (step 1, Sec. 5.2.7.2)
V3 = millilitre, volume of 0.02N H2SO4 titrant (step 3, Sec. 5.2.8.2)
W = grams, sample weight = 7.0 g (Sec. 5.2.6)
5.2.9 Alternative test procedures. The test procedures specified in this stan-
dard are traditional in nature and have been widely used throughout the water
industry. Alternative procedures may be acceptable by mutual consent between the
purchaser and supplier.
with Sec. 5.1. In the event that the results obtained by the supplier on retesting do
not agree with the test results obtained by the purchaser, the other sealed sample
shall be forwarded, unopened, for analysis to a referee laboratory agreed on by both
parties. The results of the referee analysis shall be accepted as final.
SECTION 6: DELIVERY*
Sec. 6.1 Marking
6.1.1 Required. Each shipment of material shall carry with it some means of
identification. The net weight of the contents, the name of the manufacturer, and the
brand name, if any, shall be marked legibly on each package, drum, or other
container. Other markings as required by applicable laws and regulations shall be
marked legibly on each package. When shipped in bulk, this information shall be
provided in accordance with applicable regulations.
6.1.2 Optional. The container may also bear the statement “This material
meets the requirements of AWWA B405-00, Standard for Sodium Aluminate,”
provided that the requirements of this document are met and the material is not of a
different quality in separate agreement between the supplier and purchaser.