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GB/T 35828-2018 PDF English


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GB/T 35828-2018: PDF in English (GBT 35828-2018)

GB/T 35828-2018 GB NATIONAL STANDARD OF THE PEOPLE’S REPUBLIC OF CHINA ICS 71.100.70 Y 42 Determination of chromium, arsenic, cadmium, stibium, and lead in cosmetics - Inductively coupled plasma mass spectrometry ISSUED ON. FEBRUARY 06, 2018 IMPLEMENTED ON. SEPTEMBER 01, 2018 Issued by. General Administration of Quality Supervision, Inspection and Quarantine of the PRC; Standardization Administration of the PRC. Table of Contents Foreword ... 3  Introduction ... 4  1 Scope ... 5  2 Normative references ... 5  3 Principles ... 5  4 Reagents and materials ... 6  5 Instruments and equipment... 6  6 Analytical procedures ... 7  7 Result calculation ... 9  8 Recovery rate and precision ... 9  9 Tolerance ... 10  Appendix A (Informative) Operating conditions for inductively coupled plasma mass spectrometer (ICP-MS) ... 11  Determination of chromium, arsenic, cadmium, stibium, and lead in cosmetics - Inductively coupled plasma mass spectrometry 1 Scope This Standard specifies inductively coupled plasma mass spectrometry for the determination of chromium, arsenic, cadmium, stibium, and lead in cosmetics. This Standard applies to inductively coupled plasma mass spectrometry for the determination of chromium, arsenic, cadmium, stibium, and lead in cosmetics such as creams, body lotions, lip glosses, lipsticks, liquid eyeliners, liquid foundations, perfumes, nail polishes, bath foams, and shampoos. The detection limit of this Standard for the determination of chromium, arsenic, stibium, and lead is 0.07 mg/kg; the limit of quantification is 0.2 mg/kg. The detection limit for cadmium is 0.04 mg/kg; the limit of quantification is 0.1 mg/kg. 2 Normative references The following documents are indispensable for the application of this document. For the dated references, only the editions with the dates indicated are applicable to this document. For the undated references, the latest edition (including all the amendments) are applicable to this document. GB/T 6682 Water for analytical laboratory use - Specification and test methods 3 Principles After the sample is digested, it is determined by inductively coupled plasma mass spectrometer (ICP-MS). ICP-MS consists of two main parts. ion source and mass spectrometer. After the atomization of the sample solution, it is sent by the carrier gas to the ICP torch flame. Through evaporation, dissociation, atomization, ionization, and other processes, it is converted into positively charged ions. After ion focusing, it enters the mass spectrometer. In the mass spectrometer, according to the specific mass-to-charge ratio (m/z) of the element, it is separated and collected. For a certain mass-to-charge ratio, the mass spectral response value is directly proportional to the number of ions entering the mass spectrometer, that is, the mass spectral signal intensity is cosmetics, 0.5 mL~1 mL of hydrofluoric acid (4.4) can be added in advance; and then DIGEST according to the microwave digestion procedures. After the digestion is completed, acid-driving shall be carried out, to drive off the residual hydrofluoric acid. Then ADD 3 mL of nitric acid; COOL, and FILTER the digestion solution to the 50 mL colorimetric tube pre-added with 1 mL of internal standard working solution (4.10); DILUTE to volume; SHAKE it well for use. Do the blank test in the same way. 6.3 Preparation of standard series PIPETTE 0.00 mL, 1.00 mL, 5.00 mL, 10.00 mL of secondary standard intermediate solution (4.9) and 0.50 mL, 1.00 mL, 2.00 mL of primary standard intermediate solution (4.8) respectively into 100 mL volumetric flasks. Then ADD 2.00 mL of internal standard working solution (4.10) respectively; USE dilute nitric acid solution (4.3) to dilute to volume; and SHAKE well. The standard concentrations of chromium, stibium, cadmium, arsenic, and lead are 0.00 ng/mL, 1.00 ng/mL, 5.00 ng/mL, 10.00 ng/mL, 50.00 ng/mL, 100.00 ng/mL, 200.00 ng/mL. 6.4 Reference conditions for inductively coupled plasma mass spectrometer (ICP-MS) According to the interference elimination mode provided by the instrument manufacturer, optimize the determination conditions. If there is no suitable interference elimination mode, Appendix A can be referred to for optimization. 6.5 Determination After using the tuning solution to adjust each index of the instrument with the instrument sensitivity, precision (RSD), oxide, double charge, peak shape, and resolution meeting the determination requirements, the standard series, reagent blank, and sample solution are determined respectively. The determination mass of the elements to be tested and internal standard elements is shown in Table 1. ENTER each parameter; DRAW a standard curve; and calculate the regression equation. If the determination result exceeds the linear range of the standard curve, the sample shall be diluted and then determined. The blank test, except for the absence of sample, uses exactly the same analytical procedures, reagents, and dosages. The number of parallel determinations is not less than two. ......
 
Source: Above contents are excerpted from the PDF -- translated/reviewed by: www.chinesestandard.net / Wayne Zheng et al.