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Degradation of selected pharmaceuticals in aqueous solution with UV and UV/H2O2

机译:用UV和UV / H2O2降解水溶液中的某些药物

摘要

The degradation of four pharmaceutical compounds (PhACs), ibuprofen (IBU), diphenhydramine (DP), phenazone (PZ), and phenytoin (PHT) was investigated via ultraviolet (UV) photolysis and UV/H2O2 process with a low-pressure (LP) LTV lamp. For each PhAC tested, direct photolysis quantum yields at 254 nm were found to be ranging from 6.32 x 10(-2) to 2.79 x 10(-1) mol E-1 at pH 7. The second-order rate constants of the reaction between the PhACs and (OH)-O-center dot were determined to be from 4.86 x 10(9) to 6.67 x 10(9) M-1 s(-1) by using a competition kinetic model which utilized para-chlorobenzoic acid (pCBA) as a reference compound. The overall effect of (OH)-O-center dot radical scavenging from humic acid (HA) and anions HCO3-, NO3- was measured utilizing R-OH,R-UV method through examining the aqueous photodegradation of pCBA as a probe compound. Moreover, these fundamental direct and indirect photolysis parameters were applied in the model prediction for oxidation rate constants of the PhACs in UV/H2O2 process. It was found that the predicted oxidation rate constants approximated the observed ones. The results indicated that the new R-OH,R-UV probe compound method was applicable for measuring background (OH)-O-center dot radical scavenging effects in water treatment process of UV/H2O2. Furthermore, by GC-MS analysis, most of the intermediates created during the photodegradation of the selected PhACs in UV/H2O2 process were identified. For the photodegradation of PZ, a competition mechanism existed between the direct UV photolysis and the oxidation of (OH)-O-center dot. An appropriate dosage of H2O2 could hinder the occurrence of the direct photolysis. (C) 2009 Elsevier Ltd. All rights reserved.
机译:通过紫外线(UV)光解和低压(LP)的UV / H2O2工艺研究了四种药物化合物(PhAC),布洛芬(IBU),苯海拉明(DP),非那酮(PZ)和苯妥英钠(PHT)的降解)LTV灯。对于每个测试的PhAC,发现在pH 7下,在254 nm处的直接光解量子产率为6.32 x 10(-2)至2.79 x 10(-1)mol E-1。反应的二级速率常数通过使用对氯苯甲酸的竞争动力学模型,确定PhAC和(OH)-O-中心点之间的杂原子为4.86 x 10(9)至6.67 x 10(9)M-1 s(-1) (pCBA)作为参考化合物。通过检查pCBA作为探针化合物的水性光降解,使用R-OH,R-UV方法测量了从腐殖酸(HA)和阴离子HCO3-,NO3-清除(OH)-O-中心点自由基的总体效果。此外,将这些基本的直接和间接光解参数应用于模型预测的UV / H2O2过程中PhAC的氧化速率常数。发现预测的氧化速率常数近似于观察到的常数。结果表明,新的R-OH,R-UV探针复合法可用于UV / H2O2水处理过程中本底(OH)-O-中心点自由基清除作用的测定。此外,通过GC-MS分析,鉴定了在UV / H2O2过程中所选PhAC的光降解过程中产生的大多数中间体。对于PZ的光降解,在直接UV光解和(OH)-O-中心点的氧化之间存在竞争机制。适当剂量的H2O2可能会阻止直接光解的发生。 (C)2009 Elsevier Ltd.保留所有权利。

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