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CuWO4促进TiO2光催化降解水中阿特拉津

CuWO4 Promoting TiO2 Photocatalytic Degradation of Atrazine in Water

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【作者】 何德文阳洋唐建军周康根陈伟陈益清

【Author】 HE Dewen;YANG Yang;TANG Jianjun;ZHOU Kanggen;CHEN Wei;CHEN Yiqing;School of Metallurgy and Environment, Central South University;School of Construction and Environmental Engineering,Shenzhen Polytechnic;

【通讯作者】 唐建军;

【机构】 中南大学冶金与环境学院深圳职业技术学院深圳市工业节水及城市污水资源化技术重点实验室

【摘要】 以一种简单的方法制备CuWO4,并研究了CuWO4促进Ti O2光催化降解水中阿特拉津的效能及可能机理。结果表明,反应体系加入少量(50 mg/L)CuWO4显著加快Ti O2光催化降解水中阿特拉津,反应270 min降解率达92.1%,较单一Ti O2催化效率提高1.94倍;CuWO4在降解过程中显示出较强的稳定性,溶液中微量溶解的Cu2+接收电子形成Cu(II)/Cu(I)的价态变化;随CuWO4煅烧温度(100~800℃)的升高降解率先增大后下降,500℃达到最大,而Cu2+溶出率则显著降低,CuWO4-Ti O2催化体系的正效应归功于固态CuWO4;光生电子及HO·自由基及光生电子在反应体系中起主要作用。实验结果有助于其他Cu基半导体提升Ti O2催化活性的研究。

【Abstract】 CuWO4was prepared by a simple method,and Cu WO4improving photocatalytic degradation for atrazine by Ti O2as well as the possible mechanism was studied.Results showed that,an addition of a small amount of CuWO4(50 mg/L)into the reaction system could significantly enhance the efficiency of atrazine degradation,resulting in an increased degradation efficiency of 92.1%after 270 min,which was 1.94 times higher than that of the single TiO2.CuWO4showed robust stability and the slight dissolved Cu2+received e-forming behavior of Cu(II)/Cu(I)during the photocatalytic process.As the sintering temperate of Cu WO4increased(100~800℃),the degradation efficiency of atrazine increased initially and then deceased,the maximum reached at500℃,but the dissolution rate of Cu2+decreased significantly.The origin of high phtotocatalytic effect of TiO2-CuWO4was attributed to the introduction of solid Cu WO4.The photo-induced electron and HO·radical played an important role in this reaction system.The experimental results were conductive to the research of improving photocatalytic activity of TiO2with Cu-bearing semiconductors.

【关键词】 光催化阿特拉津降解钨酸铜
【Key words】 photocatalysisAtrazinedegradationCuWO4
【基金】 深圳市科学技术项目(JCYJ20170306144117642)
  • 【文献出处】 水处理技术 ,Technology of Water Treatment , 编辑部邮箱 ,2019年06期
  • 【分类号】X703
  • 【被引频次】1
  • 【下载频次】325
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