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GB/T 30647-2014 PDF English

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GB/T 30647-2014: Determination of harmful elements total content of coatings
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GB/T 30647-2014: Determination of harmful elements total content of coatings

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NATIONAL STANDARD OF THE PEOPLE’S REPUBLIC OF CHINA ICS 87.040 G 50 Determination of harmful elements total content of coatings Issued on. DECEMBER 31, 2014 Implemented on. JULY 01, 2015 Issued by. General Administration of Quality Supervision, Inspection and Quarantine; Standardization Administration of PRC.

Table of Contents

Foreword... 3 1 Scope... 4 2 Normative references... 4 3 Principle... 4 4 Reagents and materials... 4 5 Equipment... 5 6 Test procedures... 6 7 Calculation of results... 9 8 Precision... 9

Foreword

This standard was drafted in accordance with the rules given in GB/T 1.1-2009. This standard was proposed by the China Petroleum and Chemical Industry Federation. This standard shall be under the jurisdiction of the National Technical Committee for Standardization of Coatings and Pigments (SAC/TC 5). Drafting organizations of this standard. CNOOC Changzhou Coating Chemical Research Institute Co., Ltd., Guangzhou Synthetic Materials Research Institute Co., Ltd., Zhanchen Coatings Group Co., Ltd., Beijing Bihaizhou Corrosion Protection Industry Co., Ltd., Shenzhen Guangtian Decoration Group Co., Ltd., Metallurgical Industry Jianxin Materials Co., Ltd., Marine Chemical Research Institute Co., Ltd., Chongqing Sanxia Paint Co., Ltd. The main drafters of this standard. Zhang Yonggang, Huang Ning, Tan Hongyang, Yang Qi, Li Yixuan, Guo Xiaoyan, Shi Youyou, Li Jing, Xu Zhongcheng. Determination of harmful elements total content of coatings

1 Scope

This standard specifies the test method for the total content of harmful elements in coatings. This standard applies to the determination of the total content of various harmful elements in coatings, including but not limited to the exemplified elements, such as lead, cadmium, mercury, chromium, arsenic, etc.

2 Normative references

The following documents are essential to the application of 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) are applicable to this standard. GB/T 602 Chemical reagent - Preparations of standard solutions for impurity GB/T 6682-2008 Water for analytical laboratory use - Specification and test methods

3 Principle

After the coating film is dried, suitable methods such as dry ashing method, wet acid digestion method or microwave digestion method are used to remove all organic substances;

4 Reagents and materials

Only the reagents identified as analytically pure are used in the analysis test. The water used meets the requirements of grade 3 water in GB/T 6682-2008. 4.1 Nitric acid. about 65% (mass fraction). Nitric acid that has turned yellow shall not be used. 4.2 Nitric acid solution. 1.1 (volume ratio).

5 Equipment

General laboratory equipment and some of the following equipment. 5.1 Appropriate analytical instruments (such as atomic absorption spectrometer, inductively coupled plasma emission spectrometer, inductively coupled plasma mass spectrometer, etc.). 5.6 Microwave digestion apparatus. It can be closed for digestion and has a temperature control device. 5.7 Analytical balance. The accuracy is 0.1 mg. 5.8 Crucible. 50 mL. 5.9 Volumetric flask. 50 mL, 100 mL, etc. 5.10 Beaker. 50 mL, 100 mL, etc. 5.11 Pipette. 1 mL, 2 mL, 5 mL, 10 mL, etc. 5.12 Glass plate or Teflon plate. The size is 150 mm × 100 mm.

6 Test procedures

6.1 Preparation of coating film Stir the sample to be tested evenly. Prepare a mixed sample according to the product's stated ratio (no need to add a diluent). After mixing well, prepare a coating film of appropriate thickness on a glass plate or Teflon plate (see 5.12). 6.2 Preparation of test solution 6.2.1 General 6.2.1.1 This standard provides the following three test solution’s preparation methods. The laboratory may choose one of them according to the conditions. 6.2.2 Dry ashing method Weigh about 2 g (accurate to 0.1 mg) of the crushed sample. Put it into the crucible (see 5.8). Place the crucible on a hot plate (see 5.5) in a fume hood. Gradually increase the temperature of the hot plate (not exceeding 475 °C), until the sample is digested into a coke; meanwhile the volatile digestion products have been fully discharged, leaving only dried residue. Then put the crucible in a muffle furnace at (475 ± 25) °C and keep it warm until it is completely ashed. 6.2.3 Wet acid digestion Weigh about 0.5 g ~ 1 g of the crushed sample (accurate to 0.1 mg). Place it in a 50 mL beaker (see 5.10). Add 7 mL of nitric acid (see 4.1). Cover the watch glass. Heat it on a hot plate (see 5.5) to keep the solution slightly boiling for about 5 ~ 15 min. Continue to heat until white smoke is generated, but it cannot be dried. Remove the beaker from the hot plate. 6.2.4 Microwave digestion Weigh about 0.1 g ~ 0.2 g (accurate to 0.1 mg) of the crushed sample and place it in a microwave digestion tank. Add 6 mL of nitric acid (see 4.1) and 1 mL ~ 2 mL of hydrogen peroxide (see 4.4). After the reaction is stable, close the digestion tank and place it in a microwave digestion instrument (see 5.6). Set appropriate digestion conditions for digestion. 6.3 Testing 6.3.1 General For the test solution prepared in accordance with 6.2, use appropriate analytical instrument (see 5.1) to determine the content of the tested elements. When using any kind of analytical instrument for measurement, the analyst shall operate it in accordance with the instrument manual or operation manual; indicate the analytical instrument used in the test report.

7 Calculation of results

Calculate the content of the test element in the sample according to formula (1).

8 Precision

8.1 Repeatability The relative deviation of the two test results of the same operator shall be less than 10%. ......

Source: Above contents are excerpted from the full-copy PDF -- translated/reviewed by: www.ChineseStandard.net / Wayne Zheng et al.
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