Activation of peroxymonosulfate by Al2O3-based CoFe2O4 for the degradation of sulfachloropyridazine sodium: Kinetics and mechanism

Activation of peroxymonosulfate by Al2O3-based CoFe2O4 for the degradation of sulfachloropyridazine sodium: Kinetics and mechanism
复制标题

Al2O3 基 CoFe2O4 活化过一硫酸盐降解磺胺氯哒嗪钠:动力学和机理

DOI:
10.1016/j.seppur.2017.07.046
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发表时间:
2017-12
影响因子:
8.6
通讯作者:
An Na
An Na
中科院分区:
工程技术1区
文献类型:
--
作者:
Wang Qiongfang;Shao Yisheng;Gao Naiyun;Chu Wenhai;Chen Juxiang;Lu Xian;Zhu Yanping;An Na

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摘要:制备了以al_2o_3为基体的al_2o_3 (cofe_2o_4 / al_2o_3)为催化剂,活化过氧单硫酸盐(PMS)降解磺胺氯吡嗪(SCP)。总的来说,cofe2o4 / al2o3在活化PMS中的催化性能比cofe2o4更有效。考察了清除剂、PMS浓度、pH、阴离子、天然有机物质(NOM)和温度等因素的影响。SCP的氧化符合准一级动力学模型,在pH为5.00 ~ 8.00范围内氧化效果良好。清除剂的影响表明,so4 -·在氧化过程中比HO·起更大的作用。添加no3 -对去除率有较强的抑制作用,而添加no3 -对去除率几乎没有影响,而氯化物则能增强系统的降解。温度的升高极大地促进了SCP的降解。循环4次后,CoFe 2o /Al 2o _3仍具有较好的催化性能,SCP去除率达97.6%。在此基础上,对其降解机理进行了探讨。在cofe2o4 / al2o3复合材料中,al2o3仅作为基体碱,没有额外的催化性能。
Abstract Al 2 O 3-based CoFe 2 O 4 (CoFe 2 O 4/Al 2 O 3) as a catalyst was prepared to activate peroxymonosulfate (PMS) for degradation of sulfachloropyridazine (SCP). In general, the catalytic performance of CoFe 2 O 4/Al 2 O 3 in activation PMS was demonstrated more effective than CoFe 2 O 4. Several influence factors were inspected, including scavengers, PMS concentration, pH, anions, nature organic matter (NOM) and temperature. The oxidation of SCP fitted a pseudo-first-order kinetics model and was efficient with the pH from 5.00 to 8.00. The influence of scavengers demonstrated that SO 4-· played a more significant role than HO· in the oxidation process. The removal was strongly inhibited by adding NOM or HCO 3-, and almost unaffected by adding NO 3-, while chloride could enhance the degradation in the system. The increasing temperature greatly promoted the degradation of SCP. After four recycles, CoFe 2 O 4/Al 2 O 3 still showed preferable catalytic performance with 97.6% removal rate of SCP. Furthermore, the degradation mechanism was explored based on the XPS results. In the composit of CoFe 2 O 4/Al 2 O 3, Al 2 O 3 had no additional catalytic performance but just as a matrix base.
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