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YS/T 896-2024 English PDF

YS/T 896: Evolution and historical versions

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YS/T 896-2024EnglishRFQ ASK 3 days [Need to translate] (Chemical analysis method for high purity niobium - Determination of trace impurity elements - Inductively coupled plasma mass spectrometry) Valid YS/T 896-2024
YS/T 896-2013English125 Add to Cart 0--9 seconds. Auto-delivery Methods for chemical analysis of high purity niobium. Determination of trace impurity element content. Inductively coupled plasma mass spectrometry Obsolete YS/T 896-2013

Basic data

Standard ID YS/T 896-2024 (YS/T896-2024)
Description (Translated English) (Chemical analysis method for high purity niobium - Determination of trace impurity elements - Inductively coupled plasma mass spectrometry)
Sector / Industry Nonferrous Metallurgy Industry Standard (Recommended)
Classification of Chinese Standard H14
Classification of International Standard 77.120.99
Date of Issue 2024-10-24
Date of Implementation 2025-05-01
Older Standard (superseded by this standard) YS/T 896-2013
Issuing agency(ies) Ministry of Industry and Information Technology
Summary This standard specifies the method for determining the content of trace impurity elements in high-purity niobium by inductively coupled plasma mass spectrometry. This standard applies to the determination of the content of trace impurity elements in high-purity niobium.

YS/T 896-2013: Methods for chemical analysis of high purity niobium. Determination of trace impurity element content. Inductively coupled plasma mass spectrometry


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Methods for chemical analysis of high purity niobium. Determination of trace impurity element content. Inductively coupled plasma mass spectrometry ICS 77.120.99 H63 People's Republic of China Nonferrous Metals Industry Standard Methods for chemical analysis of high purity niobium Determination of trace elements Inductively Coupled Plasma Mass Spectrometry Issued on. 2013-10-17 2014-03-01 implementation Ministry of Industry and Information Technology of the People's Republic of China released

Foreword

This standard was drafted in accordance with GB/T 1.1-2009 given rules. This standard by the national non-ferrous metals Standardization Technical Committee (SAC/TC243) centralized. This standard was drafted. Beijing Nonferrous Metal Research Institute, Jinchuan New Material Technology Co., Ltd., Dongfang Electric Group Emei semiconductor Material Co., Ltd. The main drafters of this standard. Zhangdian Kai, LI Yan-fen, Liu Ying, Sun Zeming, Tong Jian, Zang Muwen, Zhangjiang Feng, Qiu Ping, Wen-ying. Methods for chemical analysis of high purity niobium Determination of trace elements Inductively Coupled Plasma Mass Spectrometry

1 Scope

This standard specifies the niobium of high purity lithium, beryllium, boron, magnesium, titanium, vanadium, manganese, iron, cobalt, nickel, copper, zinc, gallium, arsenic, strontium, zirconium, tantalum, molybdenum, cadmium, tin, antimony, Hafnium, tungsten, lead, and the determination of bismuth content. This standard applies to the determination of trace impurities in high purity niobium. Measurement range. 0.0001% to 0.010%.

2 Method summary

Sample with nitric acid and hydrofluoric acid dissolved rhodium internal standard calibration, inductively coupled plasma mass spectrometry directly it determined by the curve Method to calculate the concentration of each element to represent the mass fraction measurement results.

3 Reagents

Unless otherwise indicated, the reagents used in the analysis are excellent pure; the water is a water. 3.1 Hydrofluoric acid (ρ = 1.16g/mL). 3.2 nitric acid (ρ = 1.42g/mL). 3.3 nitric acid (11). 3.4 lithium, beryllium, boron, magnesium, titanium, vanadium, manganese, iron, cobalt, nickel, copper, zinc, gallium, arsenic, strontium, zirconium, tantalum, molybdenum, cadmium, tin, antimony, hafnium, tungsten, lead, bismuth and rhodium unit Prime standard stock solution (national standard sample/national standard), the concentration of 1000μg/mL. 3.5 mixed standard solution A. Pipette each element separately 10.00mL standard stock solution (except rhodium element) (3.4) in 1000mL plastic Flask, additional 2mL of hydrofluoric acid (3.1), 20mL of nitric acid (3.3), dilute to the mark and mix. This solution 1mL containing lithium, beryllium, Boron, magnesium, titanium, vanadium, manganese, iron, cobalt, nickel, copper, zinc, gallium, arsenic, strontium, zirconium, tantalum, molybdenum, cadmium, tin, antimony, hafnium, tungsten, lead, bismuth each 10μg. 3.6 mixed standard solution B. Pipette 10.00mL mixed standard solution A (3.5) in 100mL plastic flask, nitric acid supplemented with 2mL (3.2), dilute to the mark and mix. This solution 1mL containing lithium, beryllium, boron, magnesium, titanium, vanadium, manganese, iron, cobalt, nickel, copper, zinc, gallium, arsenic, strontium, Zirconium, tantalum, molybdenum, cadmium, tin, antimony, hafnium, tungsten, lead, bismuth each 1μg, the time is now equipped with. 3.7 rhodium internal standard solution. Pipette 1.00mL rhodium-element standard stock solution (3.4) in a plastic 1000mL volumetric flask, dilute to the mark with water Degree, and mix. This solution 1mL rhodium-containing 1μg.

4 Instrument

4.1 Inductively coupled plasma mass spectrometry. mass resolution better than 0.8u (10% peak height); with hydrofluoric acid resistant sample introduction system; with To eliminate interfering ions such as 38Ar1H, 40Ar and 40Ar16O and other components. 4.2 Determination of isotopes of the elements shown in Table 1.