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机构地区:[1]漳州职业技术学院食品与生物工程系,福建漳州363000 [2]中山大学化学与化学工程学院,广东广州510275
出 处:《冶金分析》2013年第12期47-51,共5页Metallurgical Analysis
摘 要:在pH 5.0的HAc-NaAc缓冲溶液介质中,以增敏剂十六烷基三甲基溴化铵(CT-MAB)及活化剂邻菲啰啉(phen)共同作用下,Cr(Ⅵ)对过氧化氢氧化茜素红(ARS)褪色有明显的催化作用,建立了动力学光度法测定痕量Cr(Ⅵ)的新方法,并研究了影响催化褪色反应的因素.在选定的实验条件下,非催化反应体系与催化反应体系最大吸收波长均为553 nm,Cr(Ⅵ)的质量浓度在0.001~0.10 μg/mL呈良好的线性关系,回归方程为:△A =9.404ρ(μg/mL)-0.020 7,相关系数r=0.998 1,检出限为0.80 ng/mL.方法应用于水样及土壤样品中铬(Ⅵ)的测定,结果与原子吸收光谱法相符,相对标准偏差(RSD,n=6)为1.7%~3.0%.In pH 5. 0 HAc-NaAc buffer solution medium, with cetyl trimethyl ammonium bromide (CTMAB) as sensitizer and phenanthroline (phen) as activator, Cr (Ⅵ) had a significant catalytic effect on the oxidizing discoloration reaction between alizarin red (ARS) and hydrogen peroxide, so a novel method for the determination of trace Cr(Ⅵ) was established by kinetic spectrophotometry and the in- fluence factors on the catalytic discoloration reaction were examined. Under the selected experimental conditions, the non-catalytic reaction system and the catalytic system had the same maximum absorp- tion wavelength at 553 nm, and Cr(Ⅵ) in the concentration range of 0. 001-0.10 μg/mL showed a good linear relationship. The regression equation was △A = 9.40ρ (μg/mL) -- 0. 020 7 with correlation coefficient r = 0. 998 1 and detection limit of 0.80 ng/mL. The method was applied to the determina- tion of chromium in water and soil samples. The results were consistent with those obtained by atomic absorption spectrometry, and the relative standard deviation (RSD, n=6) was 1.7%-3.0%.
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