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紫外光 A/TiO₂光催化矿化可待因:动力学、中间产物及途径。

Photocatalytic mineralization of codeine by UV-A/TiO₂--Kinetics, intermediates, and pathways.

机构信息

Graduate Institute of Environmental Engineering, National Taiwan University, Taipei 106, Taiwan, ROC.

Graduate Institute of Environmental Engineering, National Taiwan University, Taipei 106, Taiwan, ROC.

出版信息

J Hazard Mater. 2016 Jan 15;301:137-44. doi: 10.1016/j.jhazmat.2015.08.030. Epub 2015 Aug 22.

Abstract

This study investigated the photocatalytic degradation of codeine by UV-irradiated TiO2. The degradation kinetics was determined under varied conditions including the TiO2 loading, codeine concentration, and pH. Codeine and several reaction intermediates including morphine were identified and tracked during degradation using HPLC/MS-MS technique, along with TOC and IC measurements. Specifically, removal of 100 μg/L of spike codeine was complete in 3 min by contact with a 0.1 g/L suspension of TiO2 under UV irradiation at pH 7. The degradation kinetics of codeine was first-order with respect to both the catalyst TiO2 and the reactant codeine, with enhanced reaction rates with increasing pH up to pH 9. Mineralization of codeine was possible upon prolonged contact; near complete mineralization of 10 mg/L of codeine was achieved in 90 min with 0.1 g/L TiO2 under irradiation at pH 5, during which the organic nitrogen was converted to NH3-N (74%) and NO3-N (22%). Based on the identified intermediates, two degradation pathways were proposed of which one involved ipso-substitution followed by cleavage of the aromatic ring and another involved repeated hydroxylation of the codeine molecule followed by its fragmentation.

摘要

本研究考察了 UV 辐照 TiO2 对可待因的光催化降解。在不同条件下(包括 TiO2 负载量、可待因浓度和 pH 值)下确定了降解动力学。使用 HPLC/MS-MS 技术以及 TOC 和 IC 测量,在降解过程中鉴定并跟踪了可待因和几种反应中间体,包括吗啡。具体来说,在 pH 7 下,通过与 0.1 g/L TiO2 悬浮液接触,可在 3 分钟内完全去除 100 μg/L 的加标可待因。可待因的降解动力学与催化剂 TiO2 和反应物可待因均呈一级关系,随着 pH 值的增加(最高至 pH 9),反应速率加快。在延长接触时间的情况下,可待因可以矿化;在 pH 5 下用 0.1 g/L TiO2 辐照 90 分钟,可实现 10 mg/L 可待因的近完全矿化,在此过程中,有机氮转化为 NH3-N(74%)和 NO3-N(22%)。基于鉴定出的中间体,提出了两种降解途径,一种涉及芳环的 ipso-取代和随后的断裂,另一种涉及可待因分子的重复羟基化及其随后的碎片化。

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