Yu Ping, Gao Jun-jie, Song En-jun
School of Environmental and Chemical Engineering, Shenyang Ligong University, Shenyang 110168, China.
Guang Pu Xue Yu Guang Pu Fen Xi. 2005 Oct;25(10):1674-6.
A sensitive catalytic spectrophotometric method for determining microg x L(-1) of chromium(VI) has been developed. The method, based on the catalytic effect of Cr(VI)on the oxidation of aligarin red with hydrogen peroxide, was monitored spctrophotornetrically in the medium of microemulsion which consists of CTMAB, n-pentanol, n-heptane and water. The variables affecting the rate of the reaction were investigated. The linearity range of the calibration graph is dependent on the reaction temperature. The sensitivity of this method is 72.5% higher in the microemulsion medium than in CTMAB medium. The apparent active energy of the catalytic reaction is 55.7 kJ x mol(-1). The calibration graph is linear for 2.4-75 microg x L(-1) Cr(VI)at 80 degrees C, the detection limit is 4.27 x 10(-10) g x mL(-1), and the relative standard deviation of eleven determinations of 60 microg x L(-1) Cr(VI)was 1.84%. The method has been successfully applied to the determination of chromium(IV) in the electroplating waste water.
建立了一种灵敏的催化分光光度法测定微克每升级别的六价铬。该方法基于六价铬对过氧化氢氧化酸性铬蓝K的催化作用,在由十六烷基三甲基溴化铵(CTMAB)、正戊醇、正庚烷和水组成的微乳液介质中用分光光度法进行监测。研究了影响反应速率的各种变量。校准曲线的线性范围取决于反应温度。该方法在微乳液介质中的灵敏度比在CTMAB介质中高72.5%。催化反应的表观活化能为55.7千焦每摩尔。在80℃时,校准曲线在2.4 - 75微克每升六价铬范围内呈线性,检测限为4.27×10⁻¹⁰克每毫升,对60微克每升六价铬进行十一次测定的相对标准偏差为1.84%。该方法已成功应用于电镀废水中六价铬的测定。