首页> 外文会议>Bioinformatics and Biomedical Engineering , 2009. ICBBE 2009 >Highly Sensitive Determination of Trace Molybdenum (VI) by Catalytic Kinetic Spectrophotometry
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Highly Sensitive Determination of Trace Molybdenum (VI) by Catalytic Kinetic Spectrophotometry

机译:催化动力学光度法高灵敏测定痕量钼(VI)

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A sensitive, simple, new catalytic-kinetic spectrophotometry method is proposed for determination of trace molybdenum (VI) which is based on the molybdenum's significant catalysis to the fading reaction between carboxyazo I and KIO4 which is quasi-zero-order reaction. The optimum reaction conditions were: 1.0 mL carboxyazo I, 1 mL KIO4, 2.0 mL acetate buffer of pH 5.0plusmn0.05 and at 100degC. Following the recommended procedure, the linear range of this assay was from 0.15 to 10.5 ngldrmL-1 (r=0.9967). The limit of detection was 0.03 ngldrmL-1. The relative standard deviation for the determination of 5.0 ngldrmL-1 molybdenum (VI) was below 2.1% (n=6). The proposed method was applied to the determination of molybdenum (VI) in environment water with satisfactory results.
机译:提出了一种灵敏,简单,新型的催化动力学光度法测定痕量钼(VI),该方法基于钼对羧基偶氮I和KIO 4 之间的褪色反应的显着催化作用。零级反应。最佳反应条件为:1.0 mL羧偶氮I,1 mL KIO 4 ,2.0 mL pH 5.0plusmn0.05的乙酸盐缓冲液,温度为100℃。按照推荐的程序,该测定的线性范围是0.15至10.5 ngldrmL -1 (r = 0.9967)。检测限为0.03 ngldrmL -1 。测定5.0 ngldrmL -1 钼(VI)的相对标准偏差低于2.1%(n = 6)。该方法用于环境水中的钼(VI)的测定,结果令人满意。

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