Abstract
原子吸收光谱法测定贵金属合金中的铬
Determination of Chromium in Precious Metal-based Alloys by Atomic Absorption Spectrometry
Received:May 20, 2015  
DOI:
中文关键词: 分析化学  原子吸收光谱法  贵金属合金  
英文关键词: analytical chemistry  AAS  precious metals alloys  chromium
基金项目:
Author NameAffiliationE-mail
CHEN Wen State Key Laboratory of Advanced Technologies of Comprehensive Utilization of Platinum Metals,Sino-Platinum Metals Co. Ltd., Kunming 650106, China chenwen@ipm.com.cn 
ZHAO Wenhu State Key Laboratory of Advanced Technologies of Comprehensive Utilization of Platinum Metals,Sino-Platinum Metals Co. Ltd., Kunming 650106, China  
JIN Yaqiu State Key Laboratory of Advanced Technologies of Comprehensive Utilization of Platinum Metals,Sino-Platinum Metals Co. Ltd., Kunming 650106, China  
MAO Duan State Key Laboratory of Advanced Technologies of Comprehensive Utilization of Platinum Metals,Sino-Platinum Metals Co. Ltd., Kunming 650106, China  
CHEN Guohua State Key Laboratory of Advanced Technologies of Comprehensive Utilization of Platinum Metals,Sino-Platinum Metals Co. Ltd., Kunming 650106, China  
LAI Lijun State Key Laboratory of Advanced Technologies of Comprehensive Utilization of Platinum Metals,Sino-Platinum Metals Co. Ltd., Kunming 650106, China  
LIU Li State Key Laboratory of Advanced Technologies of Comprehensive Utilization of Platinum Metals,Sino-Platinum Metals Co. Ltd., Kunming 650106, China  
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中文摘要:
      采用原子吸收光谱法测定CoCrPtSiO2、AuNiCr、NiPdCrBSi、NiCrB合金中铬含量,研究了影响铬测定的因素及其消除条件。结果表明,用盐酸-硝酸、氢氟酸密闭消解样品,高氯酸发烟驱除剩余氢氟酸,氯化铵或水合肼消除大量镍(II)、硅(IV)或金(III)的影响,用亚硫酸钠转化可将铬(VI)完全转化为高灵敏度的铬(III);标准曲线线性范围0~6.00 μg/mL,检出限0.004 μg/mL;测定含量为5%~7%的铬,相对标准偏差0.82%~1.29%,加标回收率为93.34%~110.80%。
英文摘要:
      Chromium contents in CoCrPtSiO2, AuNiCr, NiPdCrBSi, NiCrB alloy were determined by using atomic absorption spectrometry, the interference from other elements in the determination was investigated and the eliminating method was given. After the sample is transferred into the aqueous solution with a mixture of hydrochloric acid, nitric acid and hydrofluoric acid, the remaining hydrofluoric acid in the sample is dispelled by using perchloric acid. And then Ni(II) and Si(IV) are removed by precipitation with ammonium chloride, whereas Au(III) is removed by reduction with hydrazine hydrate. The conversion of Cr(VI) into Cr (III) gives rise to a final solution which will be submitted for AAS measurements. The standard working curve is linear in the range of 0~6.00 μg/mL with a detecting limit of 0.004 μg/mL. When chromium content is between 5% to 7% in the samples, the relative standard deviation can be less than 1.29%. The recovery for standard addition ranges from 93.34% to110.80%.
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