Standard Test Method for Vanadium in Water

SIGNIFICANCE AND USE
5.1 Vanadium can be found in waste that result from chemical cleaning of components in which the metal is alloyed.  
5.2 National Pollutant Discharge Elimination Systems permits or other standards, or both, require monitoring pollutants in waste discharged onto the water shed of, or into, navigable waters, and those disposed of in such a manner that eventual contamination of underground water could result.  
5.3 This test method affords an accurate and sensitive means of determining compliance or noncompliance, or both, with those permits.  
5.4 ICP-MS or ICP-AES may also be appropriate but at a higher instrument cost. See Test Methods D5673 and D1976.
SCOPE
1.1 This test method covers the determination of dissolved and total recoverable vanadium in most waters and wastewater by graphite furnace atomic absorption spectrophotometry.  
1.2 The optimum range of this test method is 10 to 200 μg/L of vanadium based on a 20-μL sample size. Concentrations higher than 200 μg/L may be determined by proper dilution of sample. A detection level as low as 4 μg/L of vanadium has been reported.  
1.3 This test method has been used successfully with reagent water, lake water, tap water, river water, condensate from a medium Btu coal gasification process, and well water. It is the user's responsibility to ensure the validity of this test method for waters of untested matrices.  
1.4 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.5 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 or regulatory limitations prior to use.  
1.6 Former Test Method A (Catalytic) was discontinued. Refer to Appendix X1 for historical information.  
1.7 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

General Information

Status
Published
Publication Date
31-May-2017
Technical Committee
Current Stage
Ref Project

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Standards Content (Sample)

This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the
Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.
Designation: D3373 − 17
Standard Test Method for
1
Vanadium in Water
This standard is issued under the fixed designation D3373; 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* 2. Referenced Documents
2
1.1 This test method covers the determination of dissolved 2.1 ASTM Standards:
and total recoverable vanadium in most waters and wastewater D1066 Practice for Sampling Steam
by graphite furnace atomic absorption spectrophotometry. D1129 Terminology Relating to Water
D1193 Specification for Reagent Water
1.2 Theoptimumrangeofthistestmethodis10to200µg/L
D1976 Test Method for Elements in Water by Inductively-
of vanadium based on a 20-µL sample size. Concentrations
Coupled Argon Plasma Atomic Emission Spectroscopy
higher than 200 µg/L may be determined by proper dilution of
D2777 Practice for Determination of Precision and Bias of
sample. A detection level as low as 4 µg/L of vanadium has
Applicable Test Methods of Committee D19 on Water
been reported.
D3370 Practices for Sampling Water from Closed Conduits
1.3 This test method has been used successfully with
D3919 Practice for Measuring Trace Elements in Water by
reagent water, lake water, tap water, river water, condensate
Graphite Furnace Atomic Absorption Spectrophotometry
from a medium Btu coal gasification process, and well water.
D4841 Practice for Estimation of Holding Time for Water
It is the user’s responsibility to ensure the validity of this test
Samples Containing Organic and Inorganic Constituents
method for waters of untested matrices.
D5673 Test Method for Elements in Water by Inductively
Coupled Plasma—Mass Spectrometry
1.4 The values stated in SI units are to be regarded as
standard. No other units of measurement are included in this D5810 Guide for Spiking into Aqueous Samples
D5847 Practice for Writing Quality Control Specifications
standard.
for Standard Test Methods for Water Analysis
1.5 This standard does not purport to address all of the
safety concerns, if any, associated with its use. It is the
3. Terminology
responsibility of the user of this standard to establish appro-
3.1 Definitions:
priate safety and health practices and determine the applica-
3.1.1 For definitions of terms used in this standard, refer to
bility or regulatory limitations prior to use.
Terminology D1129.
1.6 Former Test Method A (Catalytic) was discontinued.
Refer to Appendix X1 for historical information.
3.2 Definitions of Terms Specific to This Standard:
1.7 This international standard was developed in accor- 3.2.1 continuing calibration blank, n—a solution containing
no analytes (of interest) which is used to verify blank response
dance with internationally recognized principles on standard-
ization established in the Decision on Principles for the and freedom from carryover.
Development of International Standards, Guides and Recom-
3.2.2 continuing calibration verification, n—a solution (or
mendations issued by the World Trade Organization Technical
setofsolutions)ofknownconcentrationusedtoverifyfreedom
Barriers to Trade (TBT) Committee.
from excessive instrumental drift; the concentration is to cover
the range of calibration curve.
1
This test method is under the jurisdiction of ASTM Committee D19 on Water
and is the direct responsibility of Subcommittee D19.05 on Inorganic Constituents
2
in Water. For referenced ASTM standards, visit the ASTM website, www.astm.org, or
Current edition approved June 1, 2017. Published June 2017. Originally contact ASTM Customer Service at service@astm.org. For Annual Book of ASTM
approved in 1975. Last previous edition approved in 2012 as D3373 – 12. DOI: Standards volume information, refer to the standard’s Document Summary page on
10.1520/D3373-17. the ASTM website.
*A Summary of Changes section appears at the end of this standard
Copyright © ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959. United States
1

---------------------- Page: 1 ----------------------
D3373 − 17
3.2.3 total recoverable vanadium, n—a descriptive term 7.2 Vanadium Hollow Cathode Lamp.
relating to the metal forms of vanadium recovered in the
7.3 Graphite Furnace capable of reaching temperature suf-
acid-digestion procedure specified in this test standard.
ficient to atomize the element of interest.
4. Summary of Test Method 7.4 Graphite Tubes, pyrolytically co
...

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: D3373 − 12 D3373 − 17
Standard Test Method for
1
Vanadium in Water
This standard is issued under the fixed designation D3373; 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 This test method covers the determination of dissolved and total recoverable vanadium in most waters and wastewater by
graphite furnace atomic absorption spectrophotometry.
1.2 The optimum range of this test method is 10 to 200 μg/L of vanadium based on a 20-μL sample size. Concentrations higher
than 200μ g/L200 μg/L may be determined by proper dilution of sample. A detection level as low as 4 μg/L of vanadium has been
reported.
1.3 This test method has been used successfully with reagent water, lake water, tap water, river water, condensate from a
medium Btu coal gasification process, and well water. It is the user’s responsibility to ensure the validity of this test method for
waters of untested matrices.
1.4 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.
1.5 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 or regulatory
limitations prior to use.
1.6 Former Test Method A (Catalytic) was discontinued. Refer to Appendix X1 for historical information.
1.7 This international standard was developed in accordance with internationally recognized principles on standardization
established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued
by the World Trade Organization Technical Barriers to Trade (TBT) Committee.
2. Referenced Documents
2
2.1 ASTM Standards:
D1066 Practice for Sampling Steam
D1129 Terminology Relating to Water
D1193 Specification for Reagent Water
D1976 Test Method for Elements in Water by Inductively-Coupled Argon Plasma Atomic Emission Spectroscopy
D2777 Practice for Determination of Precision and Bias of Applicable Test Methods of Committee D19 on Water
D3370 Practices for Sampling Water from Closed Conduits
D3919 Practice for Measuring Trace Elements in Water by Graphite Furnace Atomic Absorption Spectrophotometry
D4841 Practice for Estimation of Holding Time for Water Samples Containing Organic and Inorganic Constituents
D5673 Test Method for Elements in Water by Inductively Coupled Plasma—Mass Spectrometry
D5810 Guide for Spiking into Aqueous Samples
D5847 Practice for Writing Quality Control Specifications for Standard Test Methods for Water Analysis
3. Terminology
3.1 Definitions: For definitions of terms used in this test method refer to Terminology D1129.
3.1.1 For definitions of terms used in this standard, refer to Terminology D1129.
3.2 Definitions of Terms Specific to This Standard:
1
This test method is under the jurisdiction of ASTM Committee D19 on Water and is the direct responsibility of Subcommittee D19.05 on Inorganic Constituents in Water.
Current edition approved Sept. 1, 2012June 1, 2017. Published September 2012June 2017. Originally approved in 1975. Last previous edition approved in 20072012 as
ε1
D3373 – 03 (2007)D3373 – 12. . DOI: 10.1520/D3373-12.10.1520/D3373-17.
2
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’s Document Summary page on the ASTM website.
*A Summary of Changes section appears at the end of this standard
Copyright © ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959. United States
1

---------------------- Page: 1 ----------------------
D3373 − 17
3.2.1 continuing calibration blank, n—a solution containing no analytes (of interest) which is used to verify blank response and
freedom from carryover.
3.2.2 continuing calibration verification, n—a solution (or set of solutions) of known concentration used to verify freedom from
excessive instrumental drift; the concentration is to cover the range of calibration curve.
3.2.3 total recoverable vanadium, n—dissolved vanadium plus that solu
...

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