曙红B分光光度法测定痕量铋(Ⅲ)  被引量:5

Determination of trace bismuth(Ⅲ) by spectrophotometry with eosin B

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作  者:凌立新[1] 王林[1] 

机构地区:[1]重庆文理学院化学与环境工程学院,重庆402168

出  处:《冶金分析》2010年第7期58-61,共4页Metallurgical Analysis

基  金:重庆市教育委员会资助项目(KJ051201);重庆文理学院校级重点资助项目(Z2009HH09)

摘  要:在硫酸介质中,铋(Ⅲ)对碘酸钾氧化生物染料曙红B的褪色反应有强烈催化作用,据此建立了测定痕量铋(Ⅲ)的催化动力学方法。反应最优实验条件:在25 mL测定体积中,2.0×10^-3mol/L曙红B用量为1.2 mL,1.0×10^-2mol/L碘酸钾用量为1.5 mL,反应温度为90℃。在优化条件下,体系催化反应和非催化反应的吸光度变化值(ΔA)与铋(Ⅲ)质量浓度在0-0.18μg/mL范围内呈良好线性关系。方法检出限为8.04×10^-7g/L,表观速率常数为2.97×10^-4s^-1,表观活化能为36.74 kJ/mol。对0.06 g/mL Bi(Ⅲ)标准溶液进行11次平行测定,其相对标准偏差为2.7%。本法已用于水体中痕量铋(Ⅲ)的测定,相对标准偏差(n=6)为2.8%-3.2%,与原子吸收光谱法进行了对照,结果一致。In sulphuric acid medium,bismuth(Ⅲ) had strong catalytic action on the fading reaction of biological dye eosin B oxidized by potassium iodate.Based on this,the catalytic kinetic determination of trace bismuth(Ⅲ) was established.The optimal experimental conditions were obtained: for 25 mL of solution,the dosage of eosin B(2.0×10^-3 mol/L) was 1.2 mL,the dosage of potassium iodate(1.0×10^-2 mol/L) was 1.5 mL and the reaction temperature was 90 ℃.The absorbency change(ΔA) of catalytic reaction and non-catalytic reaction showed good linear relationship with the mass concentration of bismuth(Ⅲ) in the range of 0-0.18 μg/mL.The detection limit of this method was 8.04×10^-7 g/L,the apparent reaction rate constant was 2.97×10^-4 s^-1,and the apparent activation energy was 36.74 kJ/mol.The standard solution of bismuth(Ⅲ) (0.06 g/mL) was determined for 11 times,and the relative standard deviation(RSD) was 2.7 %.The proposed method was applied to the determination of trace bismuth(Ⅲ) in water body with the relative standard deviation of 2.8 %-3.2 %,and the results were consistent with those obtained by atomic absorption spectrometry.

关 键 词:曙红B 催化动力学光度法 铋(Ⅲ) 水体 

分 类 号:O614.532[理学—无机化学]

 

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