HOME   Cart(0)   Quotation   About-Us Tax PDFs Standard-List Powered by Google www.ChineseStandard.net Database: 189760 (9 Nov 2024)

GB/T 29493.2-2013 English PDF (GB/T 29493.2-2021 Newer Version)

GB/T 29493.2-2013 (GB/T29493.2-2013, GBT 29493.2-2013, GBT29493.2-2013)
Standard IDContents [version]USDSTEP2[PDF] delivered inStandard Title (Description)StatusPDF
GB/T 29493.2-2021English350 Add to Cart 0--9 seconds. Auto-delivery Determination of harmful substances in textile dyeing and finishing auxiliaries -- Part 2: Determination of perfluorinated compounds (PFCs) Valid GB/T 29493.2-2021
GB/T 29493.2-2013English125 Add to Cart 0--9 seconds. Auto-delivery Determination of harmful substances in textile dyeing and finishing auxiliaries -- Part 2: Determination of perfluorooctane sulfonates and perfluorooctanoic acid -- HPLC-MS/MS method Obsolete GB/T 29493.2-2013
Preview PDF: GB/T 29493.2-2021    Standards related to: GB/T 29493.2-2013

BASIC DATA
Standard ID GB/T 29493.2-2013 (GB/T29493.2-2013)
Description (Translated English) Determination of harmful substances in textile dyeing and finishing auxiliaries. Part 2: Determination of perfluorooctane sulfonates and perfluorooctanoicacid. HPLC-MS/MS method
Sector / Industry National Standard (Recommended)
Classification of Chinese Standard G70
Classification of International Standard 71.100.40
Word Count Estimation 8,850
Quoted Standard GB/T 6682-2008; GB/T 8170-2008
Drafting Organization Zhejiang Communication Co., Ltd.
Administrative Organization National Fuel Standardization Technical Committee Technical Committee auxiliaries
Regulation (derived from) National Standards Bulletin 2013 No. 2
Proposing organization China Petroleum and Chemical Industry Federation
Issuing agency(ies) General Administration of Quality Supervision, Inspection and Quarantine of the People's Republic of China, Standardization Administration of the People's Republic of China
Summary This standard specifies the textile dyeing and finishing auxiliaries perfluorooctane sulfonate and perfluorooctanoic acid by high performance liquid chromatography mass spectrometry. This section applies to all types of textile dyeing and finishing auxili


GB/T 29493.2-2021 GB NATIONAL STANDARD OF THE PEOPLE’S REPUBLIC OF CHINA ICS 71.100.40 CCS G 70 Replacing GB/T 29493.2-2013 Determination of Harmful Substances in Textile Dyeing and Finishing Auxiliaries – Part 2: Determination of the Perfluorinated Compounds (PFCs) ISSUED ON: OCTOBER 11, 2021 IMPLEMENTED ON: MAY 1, 2022 Issued by: State Administration for Market Regulation; Standardization Administration of the People’s Republic of China. Table of Contents Foreword ... 3 Introduction ... 5 1 Scope ... 6 2 Normative References ... 6 3 Terms and Definitions ... 6 4 Liquid Chromatography-Tandem Mass Spectrometry (LC-MS/MS) ... 7 5 Gas Chromatography-Mass Spectrometry (GC-MS) ... 11 6 Test Report ... 16 Appendix A (Informative) Basic Information of Perfluorinated Compounds and Internal Standards Substance Tested in This Document ... 17 Appendix B (Informative) Mass Spectrometry Parameters of LC/MS/MS (ESI) for 27 Perfluorinated Compounds ... 20 Appendix C (Informative) Perfluorinated Compound Chromatograms ... 23 Appendix D (Informative) Quantitative and Qualitative Ions of GC-MS ... 33 Determination of Harmful Substances in Textile Dyeing and Finishing Auxiliaries – Part 2: Determination of the Perfluorinated Compounds (PFCs) Warning: People who use this Document shall have practical experience working in formal laboratory. This Document does not point out all possible safety issues. Users are responsible for taking appropriate safety and health measures and ensuring that the conditions specified in relevant national laws and regulations are met. 1 Scope This Document specifies the method for determining the content of 27 ionic perfluorinated compounds in textile dyeing and finishing auxiliaries by liquid chromatography-tandem mass spectrometry (LC-MS/MS); and the method for determining the content of 4 fluorinated telomer alcohols (FTOH) and 3 fluorinated acrylates (FTA) in textile dyeing and finishing auxiliaries by gas chromatography-mass spectrometry (GC-MS). This Document is applicable to the determination of 34 perfluorinated compounds (see Appendix A) in various textile dyeing and finishing auxiliaries. 2 Normative References The provisions in following documents become the essential provisions of this Document through reference in this Document. For the dated documents, only the versions with the dates indicated are applicable to this Document; for the undated documents, only the latest version (including all the amendments) is applicable to this Document. GB/T 6682 Water for analytical laboratory use - Specification and test methods GB/T 8170-2008 Rules of rounding off for numerical values & expression and judgement of limiting values 3 Terms and Definitions For the purposes of this Document, there are no terms and definitions apply. 4 Liquid Chromatography-Tandem Mass Spectrometry (LC- MS/MS) 4.1 Principle Using methanol as solvent, ultrasonic extraction of 27 ionic perfluorinated compounds in the specimen is performed; and the extract is determined and confirmed by liquid chromatography- tandem mass spectrometry; and quantified by external standard method. 4.2 Reagents or materials Unless otherwise specified, only reagents confirmed as analytically pure and Class-1 water specified in GB/T 6682 are used. 4.2.1 Methanol, chromatographically pure. 4.2.2 Acetonitrile, chromatographically pure. 4.2.3 27 ionic perfluorinated compound standard substances, purity ≥ 95% (mass fraction); see SN 1 to 27 in Table A.1. 4.2.4 Ammonium acetate aqueous solution, 5mmol/L: Accurately weigh 0.385g of ammonium acetate and dissolve it in water; transfer it to a 1L volumetric flask and dilute to the scale; and shake well. 4.2.5 Ionic perfluorinated compound standard stock solution, 200 mg/L: Accurately weigh 0.020 g (accurate to 0.1 mg) of each of the 27 ionic perfluorinated compound standard substances (4.2.3); place in a 100 mL volumetric flask; dissolve with methanol; dilute to scale; and mix well. NOTE: The ionic perfluorinated compound standard stock solution is stored at 0℃~4℃ away from light and has a shelf life of 12 months. 4.2.6 Ionic perfluorinated compound primary mixed standard intermediate solution, 2 mg/L: Accurately transfer 0.5 mL of each ionic perfluorinated compound standard stock solution (4.2.5) to a 50 mL volumetric flask; dilute with methanol (4.2.1) and make the constant volume to the scale. NOTE: The ionic perfluorinated compound primary mixed standard intermediate solution is stored at 0℃~4℃ away from light and has a shelf life of 6 months. 4.2.7 Ionic perfluorinated compound secondary mixed standard intermediate solution, 0.1 mg/L: Accurately transfer 5 mL of ionic perfluorinated compound primary mixed standard intermediate solution (4.2.6) to a 100 mL volumetric flask; dilute with methanol (4.2.1) and make constant volume to the scale. NOTE: The ionic perfluorinated compound secondary mixed standard intermediate solution shall be stored at 0℃~4℃ away from light, and the shelf life is 3 months. 4.2.8 Ionic perfluorinated compound mixed standard working solution: Accurately transfer 40μL, 100μL, 200μL, 500μL, 1000μL of ionic perfluorinated compound secondary mixed standard intermediate solution (4.2.7) to a 10 mL volumetric flask; dilute with methanol (4.2.1) and make constant volume to the scale; and prepare 0.4μg/L, 1.0μg/L, 2.0μg/L, 5.0μg/L, 10μg/L standard working solutions, respectively. NOTE: The ionic perfluorinated compounds mixed standard working solution shall be stored at 0℃~4℃ away from light and has a shelf life of 1 month. 4.3 Instruments 4.3.1 Liquid chromatography-tandem mass spectrometry: Equipped with electrospray ionization source (ESI). 4.3.2 Ultrasonic generator: Working frequency 40kHz. 4.3.3 Analytical balance: Sensitivity 0.0001g. 4.3.4 Extractor: With airtight stopper, 50mL~70mL, made of hard glass. 4.3.5 Volumetric flask: 10mL, 50mL, 100mL. 4.3.6 Disposable syringe: 1mL~5mL. 4.3.7 Regenerated cellulose (RCE) filter head: 0.45μm. NOTE: Other proven suitable filter heads can be used. 4.4 Test procedures 4.4.1 Preparation of specimen solution Accurately weigh 0.2g (accurate to 0.001g) of sample, place in the extractor; accurately add 10.0mL of methanol (4.2.1); and seal with a stopper. Place the extractor in an ultrasonic generator and extract for 30 min at room temperature; then cool to room temperature. Use a disposable syringe to filter the specimen solution through a regenerated cellulose filter head into a sample bottle; dilute it 10 times with methanol (4.2.1) and perform LC-MS/MS analysis. 4.4.2 Analysis method 4.4.2.1 Analysis conditions Since the test results depend on the used instrument, it is impossible to give general parameters for chromatographic analysis. The set parameters shall ensure that the measured component can be effectively separated from other components when measured under chromatographic 4.7 Determination lower limit, recovery rate and precision 4.7.1 Determination lower limit The determination lower limit of this Document is 0.5mg/kg. 4.7.2 Recovery rate The recovery rate of the spiked sample shall be 70%~120%. 4.7.3 Precision The absolute difference between two independent test results obtained by the same operator using the same equipment and the same test method in the same laboratory and on the same test object within a short period of time shall not exceed 10% of the arithmetic mean of the two measured values. 5 Gas Chromatography-Mass Spectrometry (GC-MS) 5.1 Principle Tert-butyl methyl ether is used as solvent; and ultrasonic extraction is used to extract the 4 fluorinated telomer alcohols (FTOH) and 3 fluorinated acrylates (FTA) in the specimen; and the determination is carried out by gas chromatography-mass spectrometry; and the internal standard method is used for quantification. 5.2 Reagents or materials Unless otherwise specified, only reagents confirmed as analytically pure and Class-1 water specified in GB/T 6682 are used. 5.2.1 Tert-butyl methyl ether. 5.2.2 4 fluorinated telomer alcohol (FTOH) standard substances, purity ≥ 95% (mass fraction), see SN 28 to 31 in Table A.1. 5.2.3 3 fluorinated acrylate (FTA) standard substances, purity ≥ 95% (mass fraction), see SN 32 to 34 in Table A.1. 5.2.4 Internal standard substance: Perfluorodecane-1,10-dicarboxylic acid dimethyl ester (CAS No.: 84750-88-9). 5.2.5 Preparation of standard stock solution, 1000 mg/L: Accurately weigh 0.100 g (accurate to 0.0001 g) of 4 fluorinated telomer alcohol (FTOH) standard substances (5.2.2) and 0.100 g (accurate to 0.0001 g) of 3 fluorinated acrylate (FTA) standard substances (5.2.3), respectively; dissolve them in tert-butyl methyl ether (5.2.1) and make constant volume to 100 mL. NOTE: The standard stock solution shall be stored at -18℃ away from light and has a shelf life of 12 months. 5.2.6 Preparation of 4 fluorotelomer alcohol (FTOH) mixed intermediate solutions, 100 mg/L: Accurately pipette 1 mL of each of the 4 fluorotelomer alcohol (FTOH) standard stock solutions (5.2.5) into a 10 mL volumetric flask; dilute with tert-butyl methyl ether (5.2.1) and make constant to the scale. NOTE: The fluorotelomer alcohol (FTOH) mixed standard intermediate solution shall be stored at -18℃ away from light and has a shelf life of 1 month. 5.2.7 Preparation of 3 fluorinated acrylate (FTA) mixed intermediate solutions, 10mg/L: Accurately transfer 0.1mL of each of the 3 fluorinated acrylate (FTA) standard stock solutions (5.2.5) into a 10mL volumetric flask; dilute with tert-butyl methyl ether (5.2.1) and make constant volume to the scale. NOTE: The fluorinated acrylate (FTA) mixed standard intermediate solution shall be stored at -18℃ away from light, and has a shelf life of 1 month. 5.2.8 Internal standard substance standard stock solution, 1000mg/L: Accurately weigh 0.010g (accurate to 0.0001g) of the internal standard substance (5.2.4); dissolve it with tert-butyl methyl ether (5.2.1) and make constant volume to 10mL. NOTE: The internal standard stock solution shall be stored at -18℃ away from light, and has the shelf life of 3 months. 5.2.9 Internal standard substance standard intermediate solution, 15 mg/L: Accurately pipette 0.15 mL of the internal standard substance standard stock solution (5.2.8) into a 10 mL volumetric flask; dilute with tert-butyl methyl ether (5.2.1) and make constant volume to the scale. NOTE: The internal standard substance standard intermediate solution shall be stored at -18°C away from light and has a shelf life of 1 month. 5.2.10 The 4 fluorinated telomer alcohols (FTOH) and 3 fluorinated acrylates (FTA) mixed standard working solutions: The preparation method is shown in Table 3. The mass concentrations of fluorinated telomer alcohols in the mixed standard working solutions are 0.02 mg/L, 0.05 mg/L, 0.1 mg/L, 0.5 mg/L, and 1 mg/L, respectively; and the mass concentrations of fluorinated acrylates are 0.2 mg/L, 0.5 mg/L, 1 mg/L, 5 mg/L, and 10 mg/L, respectively. peak area as the ordinate, and use the ratio of the target compound and internal standard concentration as the abscissa to make a standard working curve; and perform quantification by internal standard method. The response values of fluorinated telomer alcohol (FTOH) and fluorinated acrylate (FTA) in the specimen solution shall be within the linear range of instrument detection. If the content exceeds the range of the standard working curve, dilute to an appropriate concentration with tert-butyl methyl ether solution containing an internal standard concentration of 0.15 mg/L and analyze. The selected ion flow spectra of each target compound are shown in Figure C.28 of Appendix C. 5.5 Blank test Except for the addition of no sample, all the operation procedures in 5.4 are followed. 5.6 Test data processing 5.6.1 Calculation of results The test results are expressed by the test results of each fluorinated telomer alcohol (FTOH) or fluorinated acrylate (FTA). The content of each fluorinated telomer alcohol (FTOH) or fluorinated acrylate (FTA) in the sample is expressed by mass fraction, wi, and the value is expressed in mg/kg, calculated according to Formula (2): Where: Aci - the value of the peak area of the internal standard compound in the standard working solution; Ai - the value of the peak area of the target compound in the specimen solution; ρi - the value of the mass concentration of the target compound in the standard working solution, in mg/L; V - the value of the total volume of tert-butyl methyl ether used for specimen extraction, in mL; f - dilution factor; Asi - the value of the peak area of the target compound in the standard working solution; Ac - the value of the peak area of the internal standard compound in the sample solution; m - the value of the specimen mass, in g. 5.6.2 Expression of results The calculation result is expressed by the arithmetic mean of the results of two parallel determinations, rounded off to two digits after the decimal point according to the rounding value comparison method in 4.3.3 of GB/T 8170-2008. 5.7 Determination lower limit, recovery rate and precision 5.7.1 Determination lower limit The determination lower limit of this Document for fluorinated telomer alcohol (FTOH) is 10 mg/kg, and the determination lower limit for fluorinated acrylate (FTA) is 1 mg/kg. 5.7.2 Recovery rate The recovery rate of spiked samples shall be 70%~120%. 5.7.3 Precision The absolute difference between two independent test results obtained by the same operator using the same equipment and the same test method in the same laboratory and independently testing the same object within a short period of time shall not exceed 10% of the arithmetic mean of the two determination values. 6 Test Report The test report shall at least give the following: a) Sample source and description; b) This Document number; c) The used method; d) Differences from this Document; e) Abnormal conditions encountered during the test; f) Experimental results; g) Test date. ......