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GB 24409-2009 (GB 24409-2020 Newer Version) PDF English


Search result: GB 24409-2009 (GB 24409-2020 Newer Version)
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GB 24409-2020English225 Add to Cart 0-9 seconds. Auto-delivery. Limit of harmful substances of vehicle coatings Valid
GB 24409-2009English140 Add to Cart 0-9 seconds. Auto-delivery. Limit of harmful substances of automobile coatings Obsolete
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GB 24409-2009: PDF in English

ICS 87.040 G 51 NATIONAL STANDARD OF THE PEOPLE'S REPUBLIC OF CHINA Limit of Harmful Substances of Automobile Coatings ISSUED ON. SEPTEMBER 3, 2009 IMPLEMENTED ON. JUNE 1, 2010 Jointly issued by. General Administration of Quality Supervision, Inspection and Quarantine of the People’s Republic of China; Standardization Administration of the People’s Republic of China. GB 3. No action is required - Full-copy of this standard will be automatically & immediately delivered to your EMAIL address in 0~60 minutes. Contents Foreword ... II 1 Scope ... 1 2 Normative reference documents ... 1 3 Terms and Definitions ... 1 4 Product category ... 2 5 Requirement ... 2 6 Test method ... 4 7 Test rule ... 4 8 Packing mark ... 5 Annex A (Normative) Test of volatile organic compounds (VOC) content ... 6 Annex B (Normative) Tests of benzene, toluene, ethylbenzene, xylene, glycol ether and ether ester in solvent based coating ——Gas chromatography method ... 11 Annex C (Normative) Content test of glycol ether and ether ester in water paint——Gas chromatography method ... 14 Annex D (Normative) Content test of led, cadmium, mercury ... 18 Annex E (Normative) Content test of sexavalent chrome ... 23 Foreword All the technical contents in this standard are compulsory. Annex A, Annex B, Annex C, Annex D, Annex E in this standard are normative annexes. This standard is presented by the China Petroleum and Chemical Industry Association. This standard is under the centralized management of National Technical Committee of Paints & Pigments for Standardization. The main drafting organizations of this code. CNOOC Changzhou Paint & Coatings Industry Research Institute, Chery Automobile Co., Ltd., FAW Research & Development Center, BASF Coatings International Trade (Shanghai),AkzoNobel Sikkens Car Refinishes (Suzhou) Co., Ltd., Hunan Kansai Automotive Coating Co.,Ltd, Jiangsu Hongye Coatings Co.,Ltd, Hangzhou Unires Chemical Co.,Ltd, Shenzhen Pinefield Chemical Enterprises Co.,Ltd, Fujian Xin Zhan Wang Group Co., Ltd., Changzhou Planet Coatings Co.,Ltd, Jiangsu Baihe Coatings Co.,Ltd, Jiangsu Haoyue Coatings Co.,Ltd, Shenzhen Centre Testing International Corporation. The chief drafing staff of this code. Tang Ying, Chen Yuezhen, Li Daming, Zhang Guozhong, Song Hua, Li Feng, Fu Qing, Yang Pengfei, Yu Xinli, Wang Songxian, Zhang Dingde, Zhan Jianxin, Xue Fang, Bao Boqing, Jiang Chun, Guo Yong. Limit of Harmful Substances of Automobile Coatings 1 Scope This standard specifies the requirements, test method, test rules and packing mark of harmful-substance permissible limit in original coating, repair coating and spare coating used on passenger car, commercial car, trailer, road train for human and environment. This standard is applicable to all kinds of automobile coatings except putty and coating with special function. Note. in this standard the coatings with specific function are referred to the polypropylene-ground adhesion accelerant (PP water), the anti (resistant)-stone-bumping coating [except the auxiliary anti (resistant)-stone-bumping coating], the auxiliary material (joint water) to remove marks on the joint of new and old films, etc. 2 Normative reference documents The terms of the following documents in the passage of this standard become the terms of this standard. Note the date of any reference document, and its subsequent amendments all alone (not including the contents of errata) or revised edition are not applicable to this standard, however, under this standard to encourage the parties to reach an agreement to explore the possibility of using the latest version of these documents. Note the dates are not cited documents; the latest version applies to this standard. GB/T1250 Rules for expression and judgment of limiting values GB/T1725—2007 Paints varnishes and plastics—Determination of non-volatile-matter content (ISO 3251. 2003, IDT) GB/T3186 Paints varnishes and raw materials for paints and varnishes-Sampling (GB/T3186—2006, ISO15528. 2000, IDT) GB/T6682—2008 Water for laboratory use; Specifications (ISO3696. 1987, MOD) GB/T6750—2007 Paints and varnishes—Determination of density—Pyknometer method (ISO 2811-1. 1997, Paints and varnishes—Determination of density—Part1. Pyknometer method, IDT) GB/T9750 Marks for package of coating products 3 Terms and Definitions The following terms and definitions are applicable to this standard. 3.1 Solid color paints Paints of pearly-lustre-lamp effect pigment without metal. 3.2 Base coats Paints which the surface needs coating varnish. 3.3 Solid color paints without clearcoat Solid color paints which the surface needs coating varnish. 3.4 Annex A (Normative) Test of volatile organic compounds (VOC) content A.1 Principle If the organic compounds with boiling point of above 250℃ are not detected in the sample after the gas chromatography test, the tested volatile content is the VOC content of product. If the organic compounds with boiling point of above 250℃ are detected, the qualitative identification and quantitative analysis shall be carried out on the organic compounds with boiling point of above 250℃ in the sample. The volatile content deducting the content of organic compound with boiling point of above 250℃ is the VOC content of product. A.2 Material and reagent A.2.1 Carrier gas. nitrogen, purity≥99.995%. A.2.2 Fuel gas. hydrogen, purity≥99.995%. A.2.3 Combustion-supporting gas. air. A.2.4 Auxiliary gas (septum purging and tail and make-up gas). nitrogen with the same property with carrier gas. A.2.5 Internal standard. compounds which don't exist in the sample and can be separated completely from the other compositions in the chromatogram. The purity is at least 99% (mass fraction) or the known purity. For example. dimethyl phthalate, diethyl phthalate, etc. A.2.6 Calibrating compound. compounds used for calibration, the purity is at least 99% (mass fraction) or the known purity. A.2.7 Diluting solvent. organic solvents used for diluting sample without any substance of disturbing test. The purity is at least 99% (mass fraction) or the known purity. For example. ethyl acetate, etc. A.2.8 Marker. compounds used to distinguish VOC component from non-VOC component according to VOC definition. In this standard the marker is specified to be diethylene adipate (boiling point is 251℃). A.3 Instrument and equipment A.3.1 Gas chromatograph is equipped with the following equipments. A3.1.1 The injection port of divisor and the removable inner lining of vaporizing chamber. A.3.1.2 Programmed heating controller. A.3.1.3 Detector Any of the following three kinds of detectors can be used. A.3.1.3.1 Flame ionization detector (FID). A.3.1.3.2 The calibrated and tuned velocitron or other mass selective detector. A.3.1.3.3 The calibrated Fourier transform infrared spectrometry (FT-IR spectrograph). Note. if the detectors in A.3.1.3.2 or A.3.1.3.3 are adopted to process a qualitative identification to the organic compounds with boiling point of above 250℃, the apparatus shall connect with the gas chromatograph and shall be operated according to the relevant illustrations of the apparatus manufacturer. A.3.1.4 Chromatographic column. it shall be able to enough separate the measured objects, shall be used for every time to optimize the apparatus in order to make their sensitivity, stability and separating effect in the best state. The sample size and the split ratio shall be assorted to avoid beyond the chromatographic-column capacity and shall be within the linear range of apparatus detector. A.5.3.2.2 Qualitative analysis The marker (A.2.8) shall be put into the chromatograph to measure its holding time on the dimethyl polysiloxane capillary column in order to determine the integral origination in the chromatogram according to VOC definition presented in 3.4. The mixed sample shall be prepared according to the construction mixture ratio shown on product; after the even mixture, the 2g sample shall be weighed and diluted with the appropriate amount of diluents (A.2.7); the 1.0μL mixed sample is taken by sample injector (A.3.2) and put into the chromatograph; the compounds which the holding time is above marker shall be performed the qualitative identification with the chromatogram recor... ......
Source: Above contents are excerpted from the PDF -- translated/reviewed by: www.chinesestandard.net / Wayne Zheng et al.