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(X-ray diffraction method to identify the phases of imported solid wastes of metal minerals - Part 1: General rules)
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SN/T 3011.1-2020
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SN/T 3011.1-2011 | English | 239 |
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Identification of import solid waste related with metal minerals by X-ray diffraction. Part 1: General rules
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Basic data Standard ID | SN/T 3011.1-2020 (SN/T3011.1-2020) | Description (Translated English) | (X-ray diffraction method to identify the phases of imported solid wastes of metal minerals - Part 1: General rules) | Sector / Industry | Commodity Inspection Standard (Recommended) | Classification of Chinese Standard | H10 | Classification of International Standard | 77-010 | Word Count Estimation | 8,816 | Date of Issue | 2020-08-27 | Date of Implementation | 2021-03-01 | Older Standard (superseded by this standard) | SN/T 3011.1-2011 | Regulation (derived from) | General Administration of Customs Announcement No. 98 [2020] | Issuing agency(ies) | General Administration of Customs |
SN/T 3011.1-2020: (X-ray diffraction method to identify the phases of imported solid wastes of metal minerals - Part 1: General rules) ---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.
Identification of imported solid wastes phase related with metal minerals by
X-ray diffraction method-Part 1.General rules
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
Identification of the phases of imported solid wastes from metal minerals by X-ray diffraction method. Part 1.General rules
Replace SN/T 3011.1-2011
Foreword
This part is the first part of the series of standards of SN/T 3011 "Identification of the Phases of Imported Solid Wastes of Metal Minerals by X-ray Diffraction Method".
This part was drafted in accordance with the rules given in GB/T 1.1-2009.
This part replaces SN/T 3011.1-2011 "Identification of Imported Solid Wastes of Metal Minerals by X-ray Diffraction Method Part 1.General
then".
Compared with SN/T 3011.1-2011, the main technical changes in this part are as follows.
--Modified and added equipment;
--Added and improved the content of sampling and sample preparation;
--Improved the result analysis.
This part is proposed and managed by the General Administration of Customs of the People's Republic of China.
Drafting organizations of this section. Shenzhen Customs of the People’s Republic of China, Shenzhen Institute of Inspection and Quarantine, and People’s Republic of China
City Customs/Shenzhen Vocational and Technical College.
The main drafters of this section. Feng Junli, Tang Mengqi, Ye Ruijun, Li Bin, Wang Jiali, Liu Zhihong, Yu Shuyuan, Wu Jingwu, Liang
Feng, Yang Junfan, Li Yong.
The previous editions of the standards replaced by this part are as follows.
- SN/T 3011.1-2011.
X-ray diffraction method to identify imported solid metal minerals
Waste Material Phase Part 1.General Rules
Warning. The personnel using this section should have practical experience in formal laboratory work. This section does not point out all possible safety issues
question. It is the user's responsibility to take appropriate safety and health measures and to ensure compliance with the conditions stipulated by relevant national laws and regulations.
1 Scope
This part of SN/T 3011 specifies the general rules for the identification of imported solid wastes of metal minerals by X-ray diffraction.
This part is applicable to the phase identification of imported solid wastes of metal minerals by X-ray diffraction method.
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.2007.1 General Rules for Sampling and Sample Preparation of Bulk Mineral Products
3 Terms and definitions
The following terms and definitions apply to this document.
Loss of original use value or abandoned or abandoned although it has not lost the use value generated in production, life and other activities
Solid, semi-solid, and gaseous articles and substances placed in containers, as well as articles that are included in solid waste management by laws and administrative regulations,
substance.
3.2
Metal minerals
Through mining, beneficiation and smelting processes, one or more metal element or compound minerals can be extracted from it.
4 Method summary
The sample was tested with an X-ray diffractometer, and the interplanar spacing (d) and relative intensity (I) of the various diffraction peaks in the diffraction spectrum were compared with
Compare the d value and I value of the standard minerals in the diffraction spectrum library to determine whether the sample contains a certain mineral or multiple minerals.
5 Apparatus and equipment
5.1 X-ray diffractometer. equipped with inorganic standard powder diffraction database and mineral standard powder diffraction database.
5.2 Grinding machine.
5.3 Agate mortar.
5.4 Standard sieve. 147 μm, 75 μm.
5.5 Blast drying oven. the temperature can reach 105 ℃, and the temperature control accuracy is ±2 ℃.
3.1
Solid wastes
6 Sampling and sample preparation
Sampling and sample preparation are carried out in accordance with the provisions of GB.2007.1.All samples shall pass through a 147 μm standard sieve (5.4) and be kept at 105 ℃ ±2 ℃
After drying for at least 2 hours, put it in a desiccator for later use.
7 Sample test
7.1 Preparation of test pieces
Place the sample in an agate mortar (5.3) and grind until all of it passes through a 75 μm standard sieve (5.4), and take an appropriate amount of analysis sample and load it evenly
In the sample frame, use a glass sheet to compress and flatten the powder to a plane with the surface of the sample frame.
7.2 Determination
Place the sample piece on the sample table of the X-ray diffractometer (5.1), and use appropriate measurement conditions to collect the X-ray diffraction pattern of the sample.
Refer to the X-ray diffractometer measurement conditions in Appendix A.
7.3 Data analysis
Use the processing program configured with the X-ray diffractometer to analyze the X-ray diffraction pattern obtained in 7.2 to obtain the crystal plane of the sample
Spacing (d) and relative diffraction intensity (I/I0). The relative deviation of d value measurement should be less than 1%.
Use Hanawalt qualitative phase analysis method or computer search qualitative phase analysis method to determine the phase composition of the sample. Hanawalt Qualitative
Refer to the figure B.1 in Appendix B for the determination procedure of the phase analysis method, and refer to the figure in Appendix B for the determination procedure of the computer retrieval qualitative phase analysis method
B.2.
Note. Phase analysis generally needs to determine the elemental composition information of the sample in advance. The technical means to determine the elemental composition include X-ray fluorescence spectroscopy, inductance
Coupled plasma emission spectroscopy, etc.
8 Result analysis
8.1 If the main phase of the sample is a certain metallic mineral phase (that is, the strongest diffraction peak in the diffraction pattern of the sample is the strongest diffraction of a certain metallic mineral phase)
Line), or contains other metal minerals, or contains a small amount of gangue phase, then the sample is determined to be the metal mineral.
8.2 If the main phase of the sample is a certain metallic mineral phase (that is, the strongest diffraction peak in the diffraction pattern of the sample is the strongest diffraction of a certain metallic mineral phase)
Line), the non-mineral phase containing the metal or other metals is determined to contain the mineral phase of the metal and the non-mineral phase containing the metal
Phase, or non-mineral phase containing other metals.
8.3 If a certain metal mineral phase does not exist in the phase composition of the sample (that is, the strongest diffraction peak in the diffraction pattern of the sample is not a certain metal mineral phase)
The strongest diffraction line), or the non-mineral phase containing other metals, it is determined that the sample is not the metal mineral, or the non-mineral containing other metals
Physical phase.
Appendix A
(Informative appendix)
X-ray diffractometer measurement conditions
Due to the different instruments used, the optimal analysis conditions may also be different, so it is impossible to give the general parameters of the X-ray diffractometer.
The set parameters should ensure the effective collection of the X-ray diffraction pattern of the sample. The parameters given in Table A.1 have been proved to be feasible.
Note. In the measurement process, it is recommended to use an anti-air scatter shovel to remove the air scatter background in the diffraction pattern.
Appendix B
(Informative appendix)
X-ray diffraction qualitative phase analysis method
B.1 Hanawalt method
The most classic method of phase analysis is the Hanawalt method. The principle is to select three diffraction lines with the highest intensity from the diffraction lines of a substance (with
In order of decreasing intensity) and its corresponding crystal plane spacing, find the corresponding set of data in the index, and then obtain the JCPDS card
Number, find out the JCPDS card, carefully compare and compare to determine whether it contains the substance. The qualitative phase analysis steps are shown in Figure B.1.
B.2 Computer retrieval qualitative phase analysis method
With the increasing number of JCPDS cards, Hanawalt method identification takes a long time. At present, almost all X-ray diffractometers are compatible with
The computer is online, which can realize computer automatic determination and automatic retrieval, but in the end, human judgment of the retrieval result is required. Computer search
The steps of sexual phase analysis are shown in Figure B.2.
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