Standard Test Method for Water-Soluble Sulfate in Soil

SIGNIFICANCE AND USE
This test method can be used to determine if soils could have an adverse reaction with hydraulic cement concrete.
SCOPE
1.1 This test method is for the determination of water-soluble sulfate in soils.
1.2 This test method was developed for concentrations of water-soluble sulfate in soils between 0.02 and 3.33 % sulfate by mass.
1.3 This test method does not determine sulfur in any form except as sulfate.
1.4 Some governing bodies regulate the movement of soils from one area to another. It is up to the sampler and laboratory to comply with all regulations.
1.5 The values stated in SI units are to be regarded as the standard.
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 to determine the applicability of regulatory limitations prior to use.

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Historical
Publication Date
28-Feb-2005
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ASTM C1580-05 - Standard Test Method for Water-Soluble Sulfate in Soil
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NOTICE: This standard has either been superseded and replaced by a new version or withdrawn.
Contact ASTM International (www.astm.org) for the latest information
Designation:C1580–05
Standard Test Method for
Water-Soluble Sulfate in Soil
This standard is issued under the fixed designation C 1580; 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 (e) indicates an editorial change since the last revision or reapproval.
1. Scope 4. Apparatus
1.1 This test method is for the determination of water- 4.1 Photometer—One of the following, given in order of
soluble sulfate in soils. preference:
1.2 This test method was developed for concentrations of 4.1.1 Nephelometer or turbidimeter,
water-soluble sulfate in soils between 0.02 and 3.33 % sulfate 4.1.2 Spectrophotometerforuseat420nmwithlightpathof
by mass. 4 to 5 cm, and
1.3 This test method does not determine sulfur in any form 4.1.3 Filter photometer with a violet filter having a maxi-
except as sulfate. mum near 420 nm and a light path of 4 to 5 cm. Filter
1.4 Some governing bodies regulate the movement of soils photometers and photometric practices prescribed in this test
from one area to another. It is up to the sampler and laboratory method shall conform to Practice E60; spectrophotometer
to comply with all regulations. practices shall conform to Practice E 275.
1.5 The values stated in SI units are to be regarded as the 4.2 Stopwatch, readable to 0.1 minutes.
standard. 4.3 Measuring Spoon, capacity 0.2 to 0.3 mL.
1.6 This standard does not purport to address all of the 4.4 Drying oven, capable of continuously heating at 110 6
safety concerns, if any, associated with its use. It is the 5º C.
responsibility of the user of this standard to establish appro- 4.5 Balance, shall be capable of reproducing results within
priate safety and health practices and to determine the 0.0002 g with an accuracy of 60.0002 g. Direct-reading
applicability of regulatory limitations prior to use. balances shall have a sensitivity not exceeding 0.0001 g.
Conventional two-pan balances shall have a maximum sensi-
2. Referenced Documents
bility reciprocal of 0.0003 g. Any rapid weighing device that
2.1 ASTM Standards:
may be provided, such as a chain, damped motion, or heavy
C114 Test Methods for Chemical Analysis for Hydraulic
riders, shall not increase the basic inaccuracy by more than
Cement 0.0001 g at any reading and with any load within the rated
D 1193 Specification for Reagent Water
capacity of the balance.
E 11 Specification for Wire and Cloth Sieves for Testing 4.6 Stirrer, magnetic variable speed, with a TFE-
Purposes
fluorocarboncoatedmagneticstirringrodoranoverheadstirrer
E60 Practice for Analysis of Metals, Ores, and Related with a propeller.
Materials by Molecular Absorption Spectrometry
5. Reagents and Materials
E 275 Practice for Describing and Measuring Performance
of Ultraviolet, Visible, and Near Infrared Spectrophotom- 5.1 Purity of Reagents—All reagents shall conform to the
eters specifications of the Committee on Analytical Reagents of the
American Chemical Society.
3. Significance and Use
5.2 Purity of Water—Unless otherwise indicated, reference
3.1 This test method can be used to determine if soils could to water shall be understood to mean reagent water conforming
have an adverse reaction with hydraulic cement concrete.
to Specification D 1193,Type I. Other reagent water types (See
Note 1) may be used, provided it is first ascertained that the
This test method is under the jurisdiction of ASTM Committee C09 on
ConcreteandAggregatesandisthedirectresponsibilityofSubcommitteeonC09.69
Miscellaneous Tests. Reagent Chemicals, American Chemical Society Specifications, American
Current edition approved March 1, 2005. Published April 2005. Chemical Society, Washington, DC. For suggestions on the testing of reagents not
For referenced ASTM standards, visit the ASTM website, www.astm.org, or listed by the American Chemical Society, see Analar Standards for Laboratory
contact ASTM Customer Service at service@astm.org. For Annual Book of ASTM Chemicals, BDH Ltd., Poole, Dorset, U.K., and the United States Pharmacopeia
Standards volume information, refer to the standard’s Document Summary page on and National Formulary, U.S. Pharmaceutical Convention, Inc. (USPC), Rockville,
the ASTM website. MD.
Copyright © ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959, United States.
C1580–05
water is of sufficiently high purity to permit its use without using pH paper and, if needed, neutralize each filtrate to pH of
adversely affecting the precision and bias of the test method. 7 6 1 using either 0.1N HCl or 0.1N NaOH.
8.2 Adjust the temperature of the solution in the volumetric
NOTE 1—Type II water was specified at the time of round robin testing
flasks to between 20 and 25 °C [68 to 77 °F].
of this test method.
8.3 Use an aliquot of 10 mL for specimen A1, 20 mL for
5.3 Barium Chloride—Crystals of barium chloride
specimenA2,10mLforspecimenB1,and20mLforspecimen
(BaCl ·2H O) screened to 850 to 600 µm. To prepare in the
2 2 B2. Dilute to a volume of 100 mL in a volumetric flask and
laboratory, spread crystals over a large watch glass, desiccate
follow the procedure below or Test MethodsC114. Pour the
for 24 h, screen to remove any crystals that are not 850 to 600
100 mL into a 250 mL beaker. Add 5.0 mL of conditioning
µm, and store in a clean, dry jar.
reagent. Mix by stirring with a stir bar and magnetic stirrer.
5.4 Conditioning Reagent—Place 30 mL of concentrated
Add 0.3 g of the prepared BaCl crystals using a measuring
hydrochloric acid (HCl, sp gr 1.19), 300 mLreagent water, 100
spoon and start the timer.
mL 95 % ethanol or isopropanol and 75 g sodium chloride
8.4 Stir exactly 1.0 min, at the same constant speed for all
(NaCl) in a container. Add 50 mL glycerol and mix.
determinations.
5.5 Sulfate Solution, Standard (1 mL = 0.100 mg SO )—
4 8.5 Remove the beaker from the stirrer, pour solution into
Dissolve 0.1479 g of anhydrous sodium sulf
...

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