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光催化降解动力学和机制在 TiO2 水悬浮液中的环境药物:β-受体阻滞剂为例。

Photocatalytic degradation kinetics and mechanism of environmental pharmaceuticals in aqueous suspension of TiO2: a case of beta-blockers.

机构信息

State Key Laboratory of Organic Geochemistry, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Kehua Street, Tianhe District, Guangzhou 510640, China.

出版信息

J Hazard Mater. 2010 Jul 15;179(1-3):834-9. doi: 10.1016/j.jhazmat.2010.03.079. Epub 2010 Mar 23.

Abstract

This study investigated the photocatalytic degradation of three beta-blockers in TiO(2) suspensions. The disappearance of the compounds followed pseudo-first-order kinetics according to the Langmuir-Hinshelwood model and the rate constants were 0.075, 0.072 and 0.182 min(-1) for atenolol, metoprolol and propranolol, respectively. After 240 min irradiation, the reaction intermediates were completely mineralized to CO(2) and the nitrogen was predominantly as NH(4)(+). The influence of initial pH and beta-blocker concentration on the kinetics was also studied. From adsorption studies it appears that the photocatalytic degradation occurred mainly on the surface of TiO(2). Further studies indicated that surface reaction with OH radical was principally responsible for the degradation of these three beta-blockers. The major degradation intermediates were identified by HPLC/MS analysis. Cleavage of the side chain and the addition of the hydroxyl group to the parent compounds were found to be the two main degradation pathways for all three beta-blockers.

摘要

本研究考察了三种β受体阻滞剂在 TiO2 悬浮液中的光催化降解。根据朗缪尔-欣谢尔伍德模型,化合物的消失遵循准一级动力学,阿替洛尔、美托洛尔和普萘洛尔的速率常数分别为 0.075、0.072 和 0.182 min-1。照射 240 min 后,反应中间体完全矿化为 CO2,氮主要以 NH4+形式存在。还研究了初始 pH 值和β受体阻滞剂浓度对动力学的影响。从吸附研究来看,光催化降解主要发生在 TiO2 的表面。进一步的研究表明,与 OH 自由基的表面反应是导致这三种β受体阻滞剂降解的主要原因。通过 HPLC/MS 分析鉴定了主要的降解中间产物。发现对于所有三种β受体阻滞剂,侧链的断裂和羟基的加成是两种主要的降解途径。

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