ASTM D3280-85(2014)
(Test Method)Standard Test Methods for Analysis of White Zinc Pigments
Standard Test Methods for Analysis of White Zinc Pigments
SIGNIFICANCE AND USE
4.1 White zinc pigments find considerable use in white paints, and as such it is useful to formulators and users to be able to monitor the amounts of these pigments in whole paints. It is also of interest to raw material suppliers and paint producers to check the specifications of each pigment.
SCOPE
1.1 These test methods cover procedures for the analysis of white zinc pigments.
1.2 The analytical procedures appear in the following order:
Section
Preparation of Sample
6
Zinc Oxide
Total Zinc, Using Diphenylamine as Internal Indicator
7
Total Zinc, Using Uranyl Acetate as External Indicator
8
Total Impurities
9
Total Sulfur
10
Moisture and Other Volatile Matter
11
Leaded Zinc Oxide
Total Lead
12
Total Zinc
13
Total Sulfur
14
Total Impurities
15
Moisture and Other Volatile Matter
16
Water-Soluble Salts
17
Zinc Sulfide
Zinc Oxide
18
Zinc Sulfide
19
Water-Soluble Salts
20
Moisture and Other Volatile Matter
21
Barium Sulfate
22
Titanium Dioxide
23
1.3 The values stated in SI units are to be regarded as the standard. The values given in parentheses are for information only.
1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use.
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NOTICE: This standard has either been superseded and replaced by a new version or withdrawn.
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Designation: D3280 − 85 (Reapproved 2014)
Standard Test Methods for
Analysis of White Zinc Pigments
This standard is issued under the fixed designation D3280; the number immediately following the designation indicates the year of
original adoption or, in the case of revision, the year of last revision. A number in parentheses indicates the year of last reapproval. A
superscript epsilon (´) indicates an editorial change since the last revision or reapproval.
This standard has been approved for use by agencies of the U.S. Department of Defense.
1. Scope D280 Test Methods for Hygroscopic Moisture (and Other
Matter Volatile Under the Test Conditions) in Pigments
1.1 These test methods cover procedures for the analysis of
D1193 Specification for Reagent Water
white zinc pigments.
D1394 Test Methods for Chemical Analysis of White Tita-
1.2 The analytical procedures appear in the following order:
nium Pigments
Section
E11 Specification for Woven Wire Test Sieve Cloth and Test
Preparation of Sample 6
Sieves
Zinc Oxide
Total Zinc, Using Diphenylamine as Internal Indicator 7
Total Zinc, Using Uranyl Acetate as External Indicator 8
3. Summary of Test Method
Total Impurities 9
Total Sulfur 10 3.1 Zinc Oxide:
Moisture and Other Volatile Matter 11
3.1.1 Total Zinc—Determined using diphenylamine as an
Leaded Zinc Oxide
internal indicator and also using uranyl acetate as an external
Total Lead 12
Total Zinc 13 indicator. Total impurities are calculated.
Total Sulfur 14
3.1.2 Total Sulfur—Determined as BaSO and calculated to
Total Impurities 15
sulfur.
Moisture and Other Volatile Matter 16
Water-Soluble Salts 17 3.1.3 Moisture and Volatile Matter—Determined in accor-
Zinc Sulfide
dance with Method A of Test Methods D280.
Zinc Oxide 18
Zinc Sulfide 19
3.2 Leaded Zinc Oxide:
Water-Soluble Salts 20
3.2.1 Total Lead—Determined as PbSO and calculated to
Moisture and Other Volatile Matter 21
percent PbO.
Barium Sulfate 22
Titanium Dioxide 23
3.2.2 Total Zinc—Determined on the filtrate from procedure
1.3 The values stated in SI units are to be regarded as the in 13.2.1 in accordance with methods in Sections 7 or 8.
3.2.3 Total Sulfur—Determined as BaSO and calculated to
standard. The values given in parentheses are for information
only. percent SO .
3.2.4 Total Impurities—Calculatedfromcompositionaldata.
1.4 This standard does not purport to address all of the
3.2.5 Moisture and Other Volatile Matter—Determined in
safety concerns, if any, associated with its use. It is the
accordance with Method A of Test Methods D280.
responsibility of the user of this standard to establish appro-
3.2.6 Water Soluble Salts—Determined gravimetrically.
priate safety and health practices and determine the applica-
bility of regulatory limitations prior to use. 3.3 Zinc Sulfide:
3.3.1 Total Zinc—Determined using uranyl acetate external
2. Referenced Documents
indicator in accordance with Section 9.
3.3.2 Zinc Sulfide—Determined in accordance with Sections
2.1 ASTM Standards:
8 or 9 and calculating ZnO to ZnS.
3.3.3 Water Soluble Salts—Determined in accordance with
These test methods are under the jurisdiction of ASTM Committee D01 on
Section 18.
Paint and Related Coatings, Materials, and Applications and are the direct
3.3.4 Moisture—Determined in accordance with Method A
responsibility of Subcommittee D01.31 on Pigment Specifications.
of Test Methods D280.
Current edition approved Dec. 1, 2014. Published December 2014. Originally
3.3.5 Barium Sulfate—The sample is treated with N SO
approved in 1973. Last previous edition approved in 2009 as D3280 – 85 (2009).
2 4
DOI: 10.1520/D3280-85R14.
and Na CO and the residue of BaCO is dissolved in NCl and
2 3 3
For referenced ASTM standards, visit the ASTM website, www.astm.org, or
(NH ) SO added to precipitate BaSO , which is weighed.
4 2 4 4
contact ASTM Customer Service at service@astm.org. For Annual Book of ASTM
3.3.6 Titanium Dioxide—Determined in accordance with
Standards volume information, refer to the standard’s Document Summary page on
the ASTM website. Test Methods D1394.
Copyright © ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959. United States
D3280 − 85 (2014)
NOTE 1—Detailed requirements for this sieve are given in Specification
4. Significance and Use
E11.
4.1 White zinc pigments find considerable use in white
6.3 Preserve all samples in stoppered bottles or containers.
paints, and as such it is useful to formulators and users to be
able to monitor the amounts of these pigments in whole paints.
ZINC OXIDE
It is also of interest to raw material suppliers and paint
producers to check the specifications of each pigment.
7. Total Zinc, Using Diphenylamine as Internal Indicator
5. Reagents
7.1 Reagents:
7.1.1 Diphenylamine Indicator Solution (10 g/L))—
5.1 Purity of Reagents—Reagent grade chemicals shall be
Dissolve1gof diphenylamine in 100 mL of H SO .
2 4
used in all tests. Unless otherwise indicated, it is intended that
7.1.2 Potassium Ferrocyanide (1 mL = 0.008 g Zn)—
all reagents shall conform to the specifications of the Commit-
Dissolve 35 g of K Fe(CN) ·3H O in water and dilute to 1 L
tee onAnalytical Reagents of theAmerican Chemical Society, 4 6 2
and add 0.3 g of potassium ferricyanide (K Fe(CN) ). Stan-
3 6
where such specifications are available. Other grades may be
dardize the solution by titrating against zinc (320 to 340 mg),
used, provided it is first ascertained that the reagent is of
following the procedure described in 7.2. Calculate the grams
sufficiently high purity to permit its use without lessening the
of zinc equivalent to 1.00 mL of the solution.
accuracy of the determination.
7.2 Procedure—Weigh to 0.1 mg about 0.4 g of the sample
5.2 Purity of Water—Unless otherwise indicated, references
into a tall form 400-mL beaker. Moisten with about 20 mL of
to water shall be understood to mean Type II reagent grade
water, and dissolve in 15 mLof HCl. Neutralize with NH OH,
water conforming to Specification D1193.
usinglitmusastheindicator.Addanexcessof15mLofH SO
2 4
5.3 Concentration of Reagents:
(1+2) and dilute to 200 mL. Heat to approximately 60°C, add
5.3.1 Concentrated Acids and Ammonium Hydroxide—
2 drops of diphenylamine indicator solution and while stirring
When acids and ammonium hydroxide are specified by name
vigorously, titrate with K Fe(CN) solution to the color change
4 6
or chemical formula only it should be understood that concen-
from purple to a persistent yellowish green.
trated reagents of the following specific gravities or concen-
NOTE 2—The true end point is a sharp, persistent change from a purple
trations are intended:
to a yellowish green. At the beginning of the titration, a deep blue color
Acetic acid, HC H O 99.5 %
2 3 2
is developed after addition of a few millilitres of K Fe(CN) solution.
4 6
Hydrochloric acid, HCl sp gr 1.19
About 0.5 to 1.0 mL before the true end point is reached, the solution
Hydrofluoric acid, HF 48 %
changes from a blue to a purple color.After the purple color is developed,
Nitric acid, HNO sp gr 1.42
the titration should be continued dropwise to the persistent yellowish
Sulfuric acid, H SO sp gr 1.84
2 4
green end point.
Ammonium hydroxide, NH OH sp gr 0.90
The desired specific gravities or concentrations of all other
7.3 Calculation—Calculate the percent total zinc as ZnO, A,
concentrated acids are stated whenever they are specified.
as follows:
5.3.2 Diluted Acids and Ammonium Hydroxide—
V Z 31.245
Concentrations of diluted acids and ammonium hydroxide, A 5 3100 (1)
F G
S
except when standardized, are specified as a ratio stating the
where:
number of volumes of the concentrated reagents to be diluted
with a given number of volumes of water, as in the following
V =K Fe(CN) solution required for titration of the
2 4 6
example: HCl (1+99) means 1 volume of concentrated HCl (sp
specimen, mL,
gr 1.19) diluted with 99 volumes of water. Z = zinc equivalent of the K Fe(CN) solution, g/mL,
4 6
S = specimen weight, and
6. Preparation of Sample
1.245 = molecular weight ZnO (81.38)/molecular weight Zn
(65.38).
6.1 Grind dry pigments, if lumpy or not finely ground, to a
fine powder for analysis. Large samples may be thoroughly
8. Total Zinc, Using Uranyl Acetate as External Indicator
mixed and a representative portion taken and powdered if
lumpy or not finely ground. Mix the sample in all cases
8.1 Reagents:
thoroughly before taking specimens for analysis.
8.1.1 Uranyl Acetate Indicator Solution (50 g/L)—Dissolve
5gofUO (C H O ) ·2H O in 100 mL of water and make
6.2 Separate pigments from paints or pastes, grind to a fine
2 2 3 2 2 2
slightly acid with acetic acid.
powder, pass through a 180-µm (No. 80) sieve (Note 1)to
8.1.2 Potassium Ferrocyanide, Standard Solution (1
remove any skins, thoroughly mix, and oven dry at 105°C.
Moisten such pigments after weighing with a little alcohol mL = 0.008 g Zn)—Prepare and standardize as in 7.1.2. Run a
blank titration with the same amounts of reagents and water.
before adding reagents for analysis.
Calculate the zinc equivalent of the solution as follows:
Z 5 W/~V 2 B! (2)
Reagent Chemicals, American Chemical Society Specifications, American
Chemical Society, Washington, DC. For suggestions on the testing of reagents not
where:
listed by the American Chemical Society, see Analar Standards for Laboratory
Chemicals, BDH Ltd., Poole, Dorset, U.K., and the United States Pharmacopeia
Z = zinc equivalent of the K Fe(CN) solution, g/mL,
4 6
and National Formulary, U.S. Pharmacopeial Convention, Inc. (USPC), Rockville,
W = zinc used,
MD.
D3280 − 85 (2014)
10.3 Calculation—Calculate the percent sulfur, A, as fol-
V =K Fe(CN) solution required for titration of the zinc,
4 6
lows:
mL, and
B =K Fe(CN) solution required for titration of the blank,
4 6 P 30.1374
~ !
A 5 3100 (5)
F G
mL.
S
8.2 Procedure:
where:
8.2.1 Weigh to 0.1 mg about 0.4 g of the sample into a
P = BaSO precipitate, g,
tall-form 400-mL beaker. Moisten with about 20 mL of water
S = specimen weight, g, and
and dissolve by adding 10 mL of HCl. Add NH OH until
0.1374 = molecular weight of sulfur (32.064)/molecular
slightly alkaline to litmus paper. Add HCl until just acid, and
weight BaSO (233.43).
thenadd3mLinexcess.Dilutetoabout250mLwithhotwater
and heat nearly to boiling. Titrate with K Fe(CN) solution,
4 6
11. Moisture and Other Volatile Matter
stirring constantly, until a drop of uranyl acetate indicator
11.1 Procedure—Determine moisture and other volatile
tested in a white porcelain spot plate shows a brown tinge after
matter in accordance with Method A of Test Methods D280.
standing 1 min.
8.2.2 Blank—Run a blank titration with the same amounts
LEADED ZINC OXIDE
of reagents and water.
8.3 Calculation—Calculate the percent total zinc as ZnO, A,
12. Total Lead
as follows:
12.1 Procedure:
...
This document is not an ASTM standard and is intended only to provide the user of an ASTM standard an indication of what changes have been made to the previous version. Because
it may not be technically possible to adequately depict all changes accurately, ASTM recommends that users consult prior editions as appropriate. In all cases only the current version
of the standard as published by ASTM is to be considered the official document.
Designation: D3280 − 85 (Reapproved 2009) D3280 − 85 (Reapproved 2014)
Standard Test Methods for
Analysis of White Zinc Pigments
This standard is issued under the fixed designation D3280; the number immediately following the designation indicates the year of
original adoption or, in the case of revision, the year of last revision. A number in parentheses indicates the year of last reapproval. A
superscript epsilon (´) indicates an editorial change since the last revision or reapproval.
This standard has been approved for use by agencies of the U.S. Department of Defense.
1. Scope
1.1 These test methods cover procedures for the analysis of white zinc pigments.
1.2 The analytical procedures appear in the following order:
Section
Preparation of Sample 6
Zinc Oxide
Total Zinc, Using Diphenylamine as Internal Indicator 7
Total Zinc, Using Uranyl Acetate as External Indicator 8
Total Impurities 9
Total Sulfur 10
Moisture and Other Volatile Matter 11
Leaded Zinc Oxide
Total Lead 12
Total Zinc 13
Total Sulfur 14
Total Impurities 15
Moisture and Other Volatile Matter 16
Water-Soluble Salts 17
Zinc Sulfide
Zinc Oxide 18
Zinc Sulfide 19
Water-Soluble Salts 20
Moisture and Other Volatile Matter 21
Barium Sulfate 22
Titanium Dioxide 23
1.3 The values stated in SI units are to be regarded as the standard. The values given in parentheses are for information only.
1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility
of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory
limitations prior to use.
1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility
of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory
limitations prior to use.
2. Referenced Documents
2.1 ASTM Standards:
D280 Test Methods for Hygroscopic Moisture (and Other Matter Volatile Under the Test Conditions) in Pigments
D1193 Specification for Reagent Water
D1394 Test Methods for Chemical Analysis of White Titanium Pigments
E11 Specification for Woven Wire Test Sieve Cloth and Test Sieves
3. Summary of Test Method
3.1 Zinc Oxide:
These test methods are under the jurisdiction of ASTM Committee D01 on Paint and Related Coatings, Materials, and Applications and are the direct responsibility of
Subcommittee D01.31 on Pigment Specifications.
Current edition approved July 1, 2009Dec. 1, 2014. Published July 2009December 2014. Originally approved in 1973. Last previous edition approved in 20042009 as
ε1
D3280 – 85 (2004)(2009). . DOI: 10.1520/D3280-85R09.10.1520/D3280-85R14.
For referenced ASTM standards, visit the ASTM website, www.astm.org, or contact ASTM Customer Service at service@astm.org. For Annual Book of ASTM Standards
volume information, refer to the standard’sstandard’s Document Summary page on the ASTM website.
Copyright © ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959. United States
D3280 − 85 (2014)
3.1.1 Total Zinc—Determined using diphenylamine as an internal indicator and also using uranyl acetate as an external indicator.
Total impurities are calculated.
3.1.2 Total Sulfur—Determined as BaSO and calculated to sulfur.
3.1.3 Moisture and Volatile Matter—Determined in accordance with Method A of Test Methods D280.
3.2 Leaded Zinc Oxide:
3.2.1 Total Lead—Determined as PbSO and calculated to percent PbO.
3.2.2 Total Zinc—Determined on the filtrate from procedure in 13.2.1 in accordance with methods in Sections 7 or 8.
3.2.3 Total Sulfur—Determined as BaSO and calculated to percent SO .
4 3
3.2.4 Total Impurities—Calculated from compositional data.
3.2.5 Moisture and Other Volatile Matter—Determined in accordance with Method A of Test Methods D280.
3.2.6 Water Soluble Salts—Determined gravimetrically.
3.3 Zinc Sulfide:
3.3.1 Total Zinc—Determined using uranyl acetate external indicator in accordance with Section 9.
3.3.2 Zinc Sulfide—Determined in accordance with Sections 8 or 9 and calculating ZnO to ZnS.
3.3.3 Water Soluble Salts—Determined in accordance with Section 18.
3.3.4 Moisture—Determined in accordance with Method A of Test Methods D280.
3.3.5 Barium Sulfate—The sample is treated with N SO and Na CO and the residue of BaCO is dissolved in NCl and
2 4 2 3 3
(NH ) SO added to precipitate BaSO , which is weighed.
4 2 4 4
3.3.6 Titanium Dioxide—Determined in accordance with Test Methods D1394.
4. Significance and Use
4.1 White zinc pigments find considerable use in white paints, and as such it is useful to formulators and users to be able to
monitor the amounts of these pigments in whole paints. It is also of interest to raw material suppliers and paint producers to check
the specifications of each pigment.
5. Reagents
5.1 Purity of Reagents—Reagent grade chemicals shall be used in all tests. Unless otherwise indicated, it is intended that all
reagents shall conform to the specifications of the Committee on Analytical Reagents of the American Chemical Society, where
such specifications are available. Other grades may be used, provided it is first ascertained that the reagent is of sufficiently high
purity to permit its use without lessening the accuracy of the determination.
5.2 Purity of Water—Unless otherwise indicated, references to water shall be understood to mean Type II reagent grade water
conforming to Specification D1193.
5.3 Concentration of Reagents:
5.3.1 Concentrated Acids and Ammonium Hydroxide—When acids and ammonium hydroxide are specified by name or chemical
formula only it should be understood that concentrated reagents of the following specific gravities or concentrations are intended:
Acetic acid, HC H O 99.5 %
2 3 2
Hydrochloric acid, HCl sp gr 1.19
Hydrofluoric acid, HF 48 %
Nitric acid, HNO sp gr 1.42
Sulfuric acid, H SO sp gr 1.84
2 4
Ammonium hydroxide, NH OH sp gr 0.90
The desired specific gravities or concentrations of all other concentrated acids are stated whenever they are specified.
5.3.2 Diluted Acids and Ammonium Hydroxide—Concentrations of diluted acids and ammonium hydroxide, except when
standardized, are specified as a ratio stating the number of volumes of the concentrated reagents to be diluted with a given number
of volumes of water, as in the following example: HCl (1+99) means 1 volume of concentrated HCl (sp gr 1.19) diluted with 99
volumes of water.
6. Preparation of Sample
6.1 Grind dry pigments, if lumpy or not finely ground, to a fine powder for analysis. Large samples may be thoroughly mixed
and a representative portion taken and powdered if lumpy or not finely ground. Mix the sample in all cases thoroughly before
taking specimens for analysis.
6.2 Separate pigments from paints or pastes, grind to a fine powder, pass through a 180-μm (No. 80) sieve (Note 1) to remove
any skins, thoroughly mix, and oven dry at 105°C. Moisten such pigments after weighing with a little alcohol before adding
reagents for analysis.
Reagent Chemicals, American Chemical Society Specifications, American Chemical Society, Washington, DC. For suggestions on the testing of reagents not listed by
the American Chemical Society, see Analar Standards for Laboratory Chemicals, BDH Ltd., Poole, Dorset, U.K., and the United States Pharmacopeia and National
Formulary, U.S. Pharmacopeial Convention, Inc. (USPC), Rockville, MD.
D3280 − 85 (2014)
NOTE 1—Detailed requirements for this sieve are given in Specification E11.
6.3 Preserve all samples in stoppered bottles or containers.
ZINC OXIDE
7. Total Zinc, Using Diphenylamine as Internal Indicator
7.1 Reagents:
7.1.1 Diphenylamine Indicator Solution (10 g/L))—Dissolve 1 g of diphenylamine in 100 mL of H SO .
2 4
7.1.2 Potassium Ferrocyanide (1 mL = 0.008 g Zn)—Dissolve 35 g of K Fe(CN) ·3H O in water and dilute to 1 L and add 0.3
4 6 2
g of potassium ferricyanide (K Fe(CN) ). Standardize the solution by titrating against zinc (320 to 340 mg), following the
3 6
procedure described in 7.2. Calculate the grams of zinc equivalent to 1.00 mL of the solution.
7.2 Procedure—Weigh to 0.1 mg about 0.4 g of the sample into a tall form 400-mL beaker. Moisten with about 20 mL of water,
and dissolve in 15 mL of HCl. Neutralize with NH OH, using litmus as the indicator. Add an excess of 15 mL of H SO (1+2)
4 2 4
and dilute to 200 mL. Heat to approximately 60°C, add 2 drops of diphenylamine indicator solution and while stirring vigorously,
titrate with K Fe(CN) solution to the color change from purple to a persistent yellowish green.
4 6
NOTE 2—The true end point is a sharp, persistent change from a purple to a yellowish green. At the beginning of the titration, a deep blue color is
developed after addition of a few millilitres of K Fe(CN) solution. About 0.5 to 1.0 mL before the true end point is reached, the solution changes from
4 6
a blue to a purple color. After the purple color is developed, the titration should be continued dropwise to the persistent yellowish green end point.
7.3 Calculation—Calculate the percent total zinc as ZnO, A, as follows:
V Z 31.245
A 5 3100 (1)
F G
S
where:
V = K Fe(CN) solution required for titration of the specimen, mL,
2 4 6
Z = zinc equivalent of the K Fe(CN) solution, g/mL,
4 6
S = specimen weight, and
1.245 = molecular weight ZnO (81.38)/molecular weight Zn (65.38).
8. Total Zinc, Using Uranyl Acetate as External Indicator
8.1 Reagents:
8.1.1 Uranyl Acetate Indicator Solution (50 g/L)—Dissolve 5 g of UO (C H O ) ·2H O in 100 mL of water and make slightly
2 2 3 2 2 2
acid with acetic acid.
8.1.2 Potassium Ferrocyanide, Standard Solution (1 mL = 0.008 g Zn)—Prepare and standardize as in 7.1.2. Run a blank
titration with the same amounts of reagents and water. Calculate the zinc equivalent of the solution as follows:
Z 5 W/~V 2 B! (2)
where:
Z = zinc equivalent of the K Fe(CN) solution, g/mL,
4 6
W = zinc used,
V = K Fe(CN) solution required for titration of the zinc, mL, and
4 6
B = K Fe(CN) solution required for titration of the blank, mL.
4 6
8.2 Procedure:
8.2.1 Weigh to 0.1 mg about 0.4 g of the sample into a tall-form 400-mL beaker. Moisten with about 20 mL of water and
dissolve by adding 10 mL of HCl. Add NH OH until slightly alkaline to litmus paper. Add HCl until just acid, and then add 3 mL
in excess. Dilute to about 250 mL with hot water and heat nearly to boiling. Titrate with K Fe(CN) solution, stirring constantly,
4 6
until a drop of uranyl acetate indicator tested in a white porcelain spot plate shows a brown tinge after standing 1 min.
8.2.2 Blank—Run a blank titration with the same amounts of reagents and water.
8.3 Calculation—Calculate the percent total zinc as ZnO, A, as follows:
~~V 2 B!Z 31.245!
A 5 3100 (3)
F G
S
where:
V = K Fe(CN) solution required for titration of the sample, mL,
4 6
S = sample used, g, and
1.245 = molecular weight ZnO (81.38)/molecular weight Zn (65.38).
D3280 − 85 (2014)
9. Total Impurities
9.1 Calculation—Calculate the percent total impurities, A, as follows:
A 5 100 2 ~L1Z 1S ! (4)
1 5
where:
L = total lead as PbO, %,
Z = total zinc as ZnO, %, and
S = total sulfur as SO , %.
5 3
10. Total Sulfur
10.1 Reagents:
10.1.1 Bromine Water (saturated).
10.1.2 Aluminum—Reagent grade granular aluminum.
10.1.3 Barium Chloride Solution (100 g BaCl L)—Dissolve 117 g BaCl ·2H O in water and dilute to 1 L.
2 2 2
10.2 Procedure:
10.2.1 Weigh to 0.1 g about 10 g of the sample into a 400- mL beaker. Add 50 mL of saturated bromine water, 100 mL of water,
and 35 mL of HCl. Boil until all the bromine has been expelled, cool, and add 3 to 5 g of granular aluminum. Heat to boiling, filter,
and wash well with hot water.
10.2.2 Dilute the filtrate to 300 mL with water, neutralize with NH OH, and add 6 drops of HCl. Heat to boiling and add 25
mL of hot BaCl solution dropwise, with constant stirring. Allow to stand in a warm place for at least 2 h.
10.2.3 Filter, using a weighed Gooch crucible, or a fine textured filter paper and wash well with hot water. Dry and ignite in
a muffle furnace for 30 min. Cool and weigh as BaSO .
10.3 Calculation—Calculate the percent sulfur, A, as follows:
P 30.1374
~ !
A 5 3100 (5)
F G
S
where:
P = BaSO precipitate, g,
S = specimen weight, g, and
0.1374 = molecular weight of sulfur (32.064)/molecular weight BaSO (233.43).
11. Moisture and Other Volatile Matter
11.1 Procedure—Determine moisture and other volatile matter in accordance with Method A of Test Methods D280.
LEADED ZINC OXIDE
12. Total Lead
12.1 Procedure:
12.1.1 Weigh to the nearest 0.1 mg about 0.5 g of the sample into a 400-mL beaker. Dissolve in 250 mL of water and 20 mL
of HNO (Note 2). Add 5 mL of H SO and evaporate to dense white fumes. Cool, add 50 mL of 95 % alcohol and 200 mL of
3 2 4
water, and let stand cold 1 to 2 h. Filter, using a weighed Gooch crucible. Wash the precipitate with H SO (1+99) and combine
2 4
the filtrate and washings. If the zinc content of the sample is known to be 40 % or over, reserve the filtrate and washings for the
determination of total zinc (Section 13).
NOTE 3—If the sample contains calcium or barium, the lead and zinc should be separated by precipitation with H S after solution in HCl, making
alkaline with NH OH and then acid with acetic acid. Dissolve the PbS and ZnS in dilute HNO and determine the lead and zinc as above.
4 3
12.1.2 Ignite the precipitate in the crucible at dull red heat (550 6 50°C) for 20 min, cool, and weigh.
12.2 Calculation—Calculate the percent total lead as PbO, A, as follows:
~P 30.736!
A 5 3100 (6)
F G
S
where:
P = PbSO precipitate, g,
1 4
S = sample used, g, and
0.736 = molecular weight PbO (223.21)/molecular weight PbSO (303.28).
D3280 − 85 (2014)
13. Total Zinc
13.1 Reagents—See 7.1 or 8.1, whichever is applicable.
13.2 Procedure:
13.2.1 If the zinc content of the sample is known to be 40 % or over, determine zinc on the filtrate obtained in 12.1.1. If the
zinc content is known to be under 40 %, weigh to the nearest 0.1 mg about 1 g of the sample, precipitate and filter off the lead
as PbSO as described in 12.1.1, and determine zinc on the filtrate.
13.2.2 Evaporate the appropriate filtrate to dryness and determine zinc as directed in Sections 7 or 8.
14. Total Sulfur
14.1
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