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Insights into the removal of terbuthylazine from aqueous solution by several treatment methods

机译:几种处理方法从水溶液中去除叔丁嗪的见解

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摘要

This paper reports the removal of the s-triazine herbicide terbuthylazine (TBA) from aqueous solution by various treatment methods including adsorption onto activated carbon (AC) and multiwalled carbon nanotubes (MWCNT), UV254 photolysis, UV254/H2O2, single ozonation, O-3/H2O2, catalytic ozonation (AC, MWCNT and TiO2 as catalysts) and some solar driven processes such as TiO2 photocatalytic oxidation and photo-ozonation. TBA was adsorbed onto AC and MWCNT following a pseudo-second order kinetics and Freundlich isotherm. Rapid small scale column tests showed that TBA could be removed from solution by adsorption onto AC better than atrazine. The UV254/H2O2 treatment resulted in excellent removal of TBA primarily due to the oxidation capability of hydroxyl radicals (k(HO)(center dot) = 3.310(9) M-1 s(-1)) generated from H2O2 photolysis. As the H2O2 initial concentration was increased from 5 to 50 mg L-1 the HO center dot exposure per UV fluence (R-HO center dot,(UV)) increased, making the process more efficient. Single ozonation also allowed complete removal of the herbicide though the process was slow (k(03) =15.4 M-1 s(-1) at pH > 4). The ozonation process could be greatly accelerated by the enhanced generation of HO" through O-3/H2O2 and O-3/AC processes, which also led to more efficient processes in terms of ozone utilization. Commercial TiO2 (TiO2-P25) and lab prepared anatase TiO2 (TiO2-cat) nanoparticles catalyzed the removal of TBA by solar photocatalysis. In contrast, a lab prepared MWCNT-TiO2 composite was not useful as catalyst in solar photo-oxidation processes because of the HO center dot scavenging nature of the MWCNT used as support. A mechanism for TBA degradation by O-3 and HO center dot has been suggested after TBA degradation intermediates identification. (C) 2016 Elsevier Ltd. All rights reserved.
机译:本文报道了通过多种处理方法从水溶液中去除s-三嗪除草剂叔丁嗪(TBA)的方法,包括吸附到活性炭(AC)和多壁碳纳米管(MWCNT),UV254光解,UV254 / H2O2,单臭氧,O- 3 / H2O2,催化臭氧化(AC,MWCNT和TiO2作为催化剂)以及一些太阳能驱动的过程,例如TiO2光催化氧化和光臭氧化。遵循拟二级动力学和Freundlich等温线,将TBA吸附到AC和MWCNT上。快速的小规模色谱柱测试表明,通过吸附到AC上,比阿特拉津更好地从溶液中除去TBA。 UV254 / H2O2处理导致出色的TBA去除,这主要是由于H2O2光解产生的羟基自由基(k(HO)(中心点)= 3.310(9)M-1 s(-1))的氧化能力)所致。随着H2O2初始浓度从5 mg L-1增加到50 mg L-1,每个UV能量通量的HO中心点暴露量(R-HO中心点(UV))增加,从而使该过程更有效。尽管过程缓慢(在pH> 4的条件下k(03)= 15.4 M-1 s(-1)),但单次臭氧化也可以完全去除除草剂。通过O-3 / H2O2和O-3 / AC工艺增强HO“的生成,可以大大加速臭氧化过程,这也导致臭氧利用方面的效率更高。商业TiO2(TiO2-P25)和实验室制备的锐钛矿型TiO2(TiO2-cat)纳米颗粒催化太阳光催化去除TBA,相反,实验室制备的MWCNT-TiO2复合材料由于其MW中心的HO中心点清除特性而不能用作太阳光氧化过程的催化剂。在鉴定了TBA降解中间体后,提出了O-3和HO中心点降解TBA的机制(C)2016 Elsevier Ltd.保留所有权利。

著录项

  • 来源
    《Water Research》 |2016年第1期|334-343|共10页
  • 作者单位

    Univ Extremadura, Dept Ingn Quim & Quim Fis, Inst Univ Invest Agua Cambio Climat & Sostenibili, Ave Elves S-N, E-06071 Badajoz, Spain;

    Univ Extremadura, Dept Ingn Quim & Quim Fis, Inst Univ Invest Agua Cambio Climat & Sostenibili, Ave Elves S-N, E-06071 Badajoz, Spain;

    Univ Extremadura, Dept Ingn Quim & Quim Fis, Inst Univ Invest Agua Cambio Climat & Sostenibili, Ave Elves S-N, E-06071 Badajoz, Spain;

    Univ Extremadura, Dept Ingn Quim & Quim Fis, Inst Univ Invest Agua Cambio Climat & Sostenibili, Ave Elves S-N, E-06071 Badajoz, Spain;

    Univ Extremadura, Dept Ingn Quim & Quim Fis, Inst Univ Invest Agua Cambio Climat & Sostenibili, Ave Elves S-N, E-06071 Badajoz, Spain;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Adsorption; Activated carbon; Carbon nanotubes; Solar photo-ozonation; Terbuthylazine; Titania;

    机译:吸附;活性炭;碳纳米管;太阳能光臭氧化;丁苯噻嗪;二氧化钛;
  • 入库时间 2022-08-17 13:41:55

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