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作 者:葛昌华[1] 梁华定[1] 潘富友[1] 林秀丽[1]
出 处:《化学试剂》2010年第10期914-916,共3页Chemical Reagents
摘 要:研究了钒(Ⅴ)催化KBrO3氧化2-(5-羧基-1,3,4-三氮唑偶氮)-5-二乙氨基苯酚(CTZAPN)的退色反应及其动力学条件,退色反应程度与钒(Ⅴ)量在一定范围内呈线性关系,建立了测定痕量钒(Ⅴ)的催化动力学光度法。在H2SO4介质中,退色体系的最大吸收波长455 nm,钒(Ⅴ)的质量浓度在0.004~0.04μg/mL范围内符合线性关系,回归方程为ΔA=14.265 2ρ+0.002 07(ρ:μg/mL),相关系数r=0.998 7,体系的表观摩尔吸光系数为ε=7.30×105L.mol-1.cm-1,检出限为2.99×10-10g/mL。方法不经分离直接测定面粉和花生样品中的痕量钒,测定结果与AAS法的测定值相符。A new catalytic kinetic spectrophotometry for the determination of trace vanadium was established based on the catalytic action of V(Ⅴ) on the oxidative fading reaction between 2-(5-carboxy-1,3,4-triazoleazo)-5-diethylamino phenol(CTZAPN) and KBrO3 in a medium of H2SO4 and under heating conditions.The maximum absorbance was detected at 455 nm.The calibration curve was linear in the range of 0.004~0.04 mg/L for V(Ⅴ),and the linear regression equation was ΔA=14.265 2ρ+0.002 07(ρ:μg/mL) with the correlation coefficient equating to 0.998 7.The detection limit and apparent molar absorptivity were 2.99×10-10 g/mL and 7.30×105 L·mol-1·cm-1 for V(Ⅴ),respectively.The method was applied to the determination of trace vanadium in flour and peanut samples.The results were in good agreement with the values obtained by atomic absorption spectrometry.
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