کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
4481259 1623094 2015 9 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Photocatalytic degradation of methamphetamine by UV/TiO2 – Kinetics, intermediates, and products
موضوعات مرتبط
مهندسی و علوم پایه علوم زمین و سیارات فرآیندهای سطح زمین
پیش نمایش صفحه اول مقاله
Photocatalytic degradation of methamphetamine by UV/TiO2 – Kinetics, intermediates, and products
چکیده انگلیسی


• UV/TiO2 process showed promise in removing methamphetamine (MAT) and intermediates.
• Photocatalytic degradation of MAT occurred in wastewater at a reduced rate.
• MAT was mineralized after 3 h, with N conversion to NH4+ and NO3−.
• Hydroxylated MAT was authenticated and four other intermediates were identified.
• Degradation pathways involved hydroxylation of MAT and breakage of its side chain.

Methamphetamine (MAT) is a prescription drug and often a substance of abuse. It is found in WWTP influents and effluents as well as surface waters in many regions, elevating concerns about their potential impact. MAT is not effectively removed by conventional processes of domestic wastewater treatment plants (WWTPs). To contemplate advanced treatment, this study evaluates the feasibility of eliminating MAT by UV-illuminated TiO2, a potential retrofit to existing UV disinfection units. The degradation kinetics and mechanism of MAT by TiO2 under low-wattage UV illumination (9 W with maximum output at 365 nm) were investigated. Experimental parameters were varied including the TiO2 loading, MAT concentration, and pH. During treatment, MAT and its intermediates were tracked by HPLC-MS/MS, along with TOC and IC measurements to determine the mineralization extent. In contact with 0.1 g/L of TiO2 under illumination at pH 7, an entire spike amount of 100 μg/L of MAT was removed from deionized water after 3 min and 76 μg/L of MAT was removed from the secondary wastewater effluent after 30 min. The degradation of MAT followed an apparent first-order kinetics. Near complete mineralization of MAT from 10 mg/L was achieved in 180 min with 0.1 g/L of TiO2 at pH 5, by which the organic nitrogen was converted to NH4+ and NO3−. Based on identified intermediates, two degradation pathways were deduced that involved cleavage of the side chain as well as hydroxylation of the MAT compound. The photocatalytic UV/TiO2 process shows promise in arresting the release of MAT and its intermediate derivatives into the water environment.

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ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Water Research - Volume 74, 1 May 2015, Pages 1–9
نویسندگان
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