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Basic data
| Standard ID | SN/T 5237-2020 (SN/T5237-2020) |
| Description (Translated English) | (Import and export textiles. Determination of extractable heavy metals. Inductively coupled plasma mass spectrometry) |
| Sector / Industry | Commodity Inspection Standard (Recommended) |
| Classification of Chinese Standard | W04 |
| Classification of International Standard | 59.080.01 |
| Word Count Estimation | 7,719 |
| Date of Issue | 2020-08-27 |
| Date of Implementation | 2021-03-01 |
| Regulation (derived from) | General Administration of Customs Announcement No. 98 [2020] |
| Issuing agency(ies) | General Administration of Customs |
SN/T 5237-2020: (Import and export textiles. Determination of extractable heavy metals. Inductively coupled plasma mass spectrometry)
---This is a DRAFT version for illustration, not a final translation. Full copy of true-PDF in English version (including equations, symbols, images, flow-chart, tables, and figures etc.) will be manually/carefully translated upon your order.
Textiles for import and export-Determination of extractable heavy metals-
Inductively coupled plasma mass spectrometry method
The People's Republic of China Entry-Exit Inspection and Quarantine Industry Standards
Issued by the General Administration of Customs of the People's Republic of China
2020-08-27 release
2021-03-01 implementation
Import and export textiles. Determination of extractable heavy metals. Inductively coupled plasma mass spectrometry
Foreword
This standard was drafted in accordance with the rules given in GB/T 1.1-2009.
This standard was proposed and managed by the General Administration of Customs of the People's Republic of China.
This standard was drafted by. Weifang Customs of the People's Republic of China/Weifang Product Quality Inspection Institute.
The main drafters of this standard. Zhang Jinling, Wang Liangliang, Ding Kuiying, Tian Guoning, Li Kai, Liu Dongxia, Sun Jun, Guo Liqiang.
Determination of extractable heavy metals in textiles for import and export
Inductively coupled plasma mass spectrometry
Warning-personnel using this standard should have practical experience in formal laboratory work. This standard does not point out all possible safety issues
question. The user is responsible for taking appropriate safety and health measures and ensuring compliance with the conditions stipulated by relevant national laws and regulations.
1 Scope
This standard specifies the use of inductively coupled plasma mass spectrometer (ICP-MS) to extract heavy metals such as lead (Pb) and cadmium in textiles.
(Cd), Chromium (Cr), Arsenic (As), Copper (Cu), Antimony (Sb), Nickel (Ni), Cobalt (Co), Mercury (Hg) 9 simultaneous determination method.
This standard applies to the determination of extractable heavy metals in various textile materials and their products.
2 Normative references
The following documents are indispensable for the application of this document. For dated reference documents, only the dated version applies to this article
Pieces. For undated reference documents, the latest version (including all amendments) is applicable to this document.
GB/T 602 Preparation of standard solutions for impurity determination of chemical reagents
GB/T 3922 Textile color fastness test Color fastness to perspiration
GB/T 6682 Analytical laboratory water specifications and experimental methods
3 Principle
The sample was extracted with artificial acid sweat, filtered, and measured with an inductively coupled plasma mass spectrometer. Qualitative by element specific mass number
Analysis, quantitative analysis with internal standard method.
4 Reagents and materials
Unless otherwise specified, all reagents used are pure superior grade, and the experimental water is secondary water that meets the requirements of GB/T 6682.
4.1 Potassium dichromate.
4.2 Hydrochloric acid. The mass concentration is 36%～38%.
4.3 Nitric acid. The mass concentration is 65%～68%.
4.4 2% hydrochloric acid solution (volume concentration).
4.5 1% nitric acid solution (volume concentration).
4.6 5% nitric acid solution (volume concentration).
4.7 20% nitric acid solution (volume concentration).
4.8 Nitric acid solution of potassium dichromate (0.5 g/L). Weigh 0.05 g of potassium dichromate (4.1) and dissolve in 100 mL of 5% nitric acid solution (4.6).
4.9 Acid sweat. Use the secondary water specified in GB/T 6682 to prepare acid sweat according to GB/T 3922, and use it now.
4.10 Lead, cadmium, chromium, arsenic, copper, antimony, nickel, cobalt, mercury standard stock solution (1000 mg/L). prepared according to GB/T 602 standard or
Purchase certified reference materials directly.
4.11 Mixed standard working solution (10 mg/L). accurately pipette 0.5 mL standard stock solution of lead, cadmium, chromium, arsenic, copper, antimony, nickel, and cobalt.
The solution (4.10) is placed in a 50 mL volumetric flask, and the volume is fixed with 5% nitric acid solution (4.6) to obtain a 10 mg/L mixed standard working solution.
Store in the refrigerator away from light, and the validity period is 1 month.
4.12 Mercury standard working solution (10 mg/L). accurately pipette 0.5 mL of mercury standard stock solution (4.10) into a 50 m1 volumetric flask, use
The nitric acid solution of potassium dichromate (4.8) is fixed to a volume of 10 mg/L mercury standard working solution, and it is stored in a refrigerator at 4 ℃ and protected from light. The validity period is 2 years.
4.13 Internal standard stock solution (100 mg/L). Prepare according to GB/T 602 standard or directly purchase certified reference materials, the internal standard of each analysis element
For standard elements, see Table A.2.
4.14 Mixed internal standard working solution (1 mg/L). respectively take 0.5 mL internal standard stock solution (4.13) in a 50 mL volumetric flask, and use 1%
The volume of nitric acid solution (4.5) was fixed to obtain a mixed internal standard working solution of 1 mg/L.
4.15 Argon gas. purity ≥ 99.999%.
4.16 Helium. purity ≥ 99.999%.
5 Apparatus and equipment
5.1 Inductively coupled plasma mass spectrometer (ICP-MS).
5.2 Analytical balance. Sensitivity is 0.01 g and 0.1 mg.
5.3 Conical flask with stopper. 150 mL.
Note. Before use, soak in 20% nitric acid solution overnight, rinse with water, and finally rinse with water for more than three times and dry.
5.4 Constant temperature water bath oscillator. It can be controlled at a constant temperature (37±2)°C, and the oscillation frequency is 60 times/min.
5.5 Water filter membrane. 0.45 μm.
6 Test procedure
6.1 Preparation of extraction sample solution
Take a representative sample, cut it into small pieces below 5 mm×5 mm, mix well, weigh 4 g sample, accurate to 0.01 g, and place it in a stopper.
In the triangular flask (5.3), add 80 mL of acidic sweat (4.9), soak the fiber fully, and place it in a constant temperature water bath shaker (5.4).
After shaking for (60±5) min, take it out, let stand and cool to room temperature, filter through membrane (5.5), add 0.1 mL per 10 mL of filtrate for mercury measurement
Hydrochloric acid (4.2), add 0.05 mL of nitric acid (4.3) for every 10 mL of filtrate to test other elements, as the test solution.
6.2 Blank test
Carry out a blank test with the same product.
6.3 Preparation of standard working curve
Take a certain amount of lead, cadmium, chromium, arsenic, copper, antimony, nickel, and cobalt mixed standard working solution (4.11), use 1% nitric acid solution (4.5)
Prepare a series of standard working solutions by diluting step by step. Take a certain amount of mercury standard working solution (4.12) and dilute with 2% hydrochloric acid solution (4.4) step by step
Prepare a series of standard working solutions (the highest point does not exceed 5 μg/L).
6.4 Determination
Refer to Table A.1 to optimize the parameters of the instrument conditions. The mass number and integration time of the analysis elements are shown in Table A.2.
Solution, blank solution and sample solution. If the measurement result exceeds the range of the standard working curve, the test solution needs to be diluted before proceeding
Determination.
7 Result calculation
The content of each extractable heavy metal in the sample is calculated according to formula (1).
Xi - the content of metal element i in the sample, in milligrams per kilogram (mg/kg);
Ci-the concentration of metal element i in the sample solution, in micrograms per liter (μg/L);
Ci0-the concentration of metal element i in the blank solution, in micrograms per liter (μg/L);
V-the volume of the sample solution, the unit is milliliters (mL);
F-dilution factor;
m-the mass of the sample, in grams (g).
The calculation result retains two significant digits.
8 Low limit of determination
The lower limit of this method is shown in Table 1.
Note. The detection limits of different instruments will vary, and the lower limit of this method is for reference only.
9 Precision
In the same laboratory, the same operator uses the same equipment and according to the same test method to continuously perform the same test on the same object.
Independent test, the relative standard deviation of the two independent test results obtained is not more than 10%. With the arithmetic greater than these two measured values
It is assumed that 10% of the average value does not exceed 5%.
Appendix A
(Informative appendix)
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