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Designation D6827 − 02 (Reapproved 2016) Standard Test Method for Zinc Analysis of Floor Polishes and Floor Polish Polymers By Flame Atomic Absorption (A A )1 This standard is issued under the fixed d[.]

Designation: D6827 − 02 (Reapproved 2016) Standard Test Method for Zinc Analysis of Floor Polishes and Floor Polish Polymers By Flame Atomic Absorption (A.A.)1 This standard is issued under the fixed designation D6827; 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 5.1.1 Before a sample can be run for total zinc, it must be prepared so that any insoluble zinc will be solubilized and not removed by the filtering process By preparing the sample in the following way, the analysis will be much more accurate (testing total zinc instead of soluble zinc) The prep method will also lessen the chance of clogging the nebulizer of the atomic absorption unit with particulate matter Scope 1.1 This laboratory test method covers the analysis of floor polishes and floor polish polymers for total zinc content 1.2 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 5.2 Prep Method: 5.2.1 Important—All glassware used must be washed with 1:1 nitric acid solution and rinsed with deionized water to eliminate contamination 5.2.2 Weigh approximately 50 g of sample into a 100–mL beaker Record the exact weight to 0.001 g on the analysis sheet 5.2.3 Add approximately mL of a 1:1 nitric acid solution to the beaker The amount need not be exact Two disposable pipets worth should be adequate 5.2.4 Heat the sample to boiling in a hood Allow the sample to boil until approximately 40 mL of sample remain 5.2.5 Cool the sample and filter into a 100–mL volumetric flask Rinse the beaker and filter into the volumetric flask with deionized water 5.2.6 Bring the sample to volume with deionized water 5.2.7 Analyze sample by flame A.A Significance and Use 2.1 This test method is generally accepted for the preparation of floor polish and floor polish polymers for the analysis of total zinc content Knowing the total zinc content of a floor finish or polymer can aid in determining the proper disposal method of used or unwanted product Apparatus 3.1 Analytical Balance, accurate to 0.001 g 3.2 Hot Plate 3.3 Ventilation Hood Reagents and Materials 4.1 100 mL Beaker 4.2 1:1 Nitric Acid Solution 5.3 Sample Analysis: 5.3.1 The samples should be analyzed using a flame atomic absorption spectrometer In absence of this piece of equipment, the prepped samples may be sent to an independent laboratory for analysis as long as the following information is recorded: 5.3.1.1 Calibration curve (record concentration and absorbance of standards), 5.3.1.2 Analysis of standard at beginning and end of sample run, 5.3.1.3 Blank analysis, 5.3.1.4 Sample identification, and 5.3.1.5 Date of analysis 4.3 Disposable Pipets 4.4 100-mL Volumetric Flask 4.5 Deionized Water 4.6 Filter Funnel 4.7 Filter Paper Procedure 5.1 Sample Preparation: This test method is under the jurisdiction of ASTM Committee D21 on Polishes and is the direct responsibility of Subcommittee D21.03 on Chemical and Physical Testing Current edition approved Oct 1, 2016 Published October 2016 Originally approved in 2002 Last previous edition approved in 2008 as D6827 – 02 (2008) DOI: 10.1520/D6827-02R16 Precision and Bias 6.1 To be determined through round robin inter-laboratory participation Copyright © ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959 United States D6827 − 02 (2016) Keywords 7.1 atomic absorption; floor finish; zinc ASTM International takes no position respecting the validity of any patent rights asserted in connection with any item mentioned in this standard Users of this standard are expressly advised that determination of the validity of any such patent rights, and the risk of infringement of such rights, are entirely their own responsibility This standard is subject to revision at any time by the responsible technical committee and must be reviewed every five years and if not revised, either reapproved or withdrawn Your comments are invited either for revision of this standard or for additional standards and should be addressed to ASTM International Headquarters Your comments will receive careful consideration at a meeting of the responsible technical committee, which you may attend If you feel that your comments have not received a fair hearing you should make your views known to the ASTM Committee on Standards, at the address shown below This standard is copyrighted by ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959, United States Individual reprints (single or multiple copies) of this standard may be obtained by contacting ASTM at the above address or at 610-832-9585 (phone), 610-832-9555 (fax), or service@astm.org (e-mail); or through the ASTM website (www.astm.org) Permission rights to photocopy the standard may also be secured from the Copyright Clearance Center, 222 Rosewood Drive, Danvers, MA 01923, Tel: (978) 646-2600; http://www.copyright.com/

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