石墨氮化碳
化学
光催化
降级(电信)
纳米复合材料
核化学
氮化碳
无机化学
材料科学
催化作用
纳米技术
有机化学
计算机科学
电信
作者
Changsheng Guo,Miao Chen,Linlin Wu,Yingying Pei,Chunhua Hu,Yuan Zhang,Jian Xu
出处
期刊:ACS applied nano materials
[American Chemical Society]
日期:2019-04-10
卷期号:2 (5): 2817-2829
被引量:33
标识
DOI:10.1021/acsanm.9b00295
摘要
As one of the most abused illicit drugs, ketamine (KET) has been widely detected in different water environments around the globe, which necessitates the development of effective approaches for KET removal from water. In the present study, several novel Ag3PO4/P-g-C3N4 heterojunction composites were successfully constructed using an in situ growth method, and the samples were characterized by a series of instruments. The synthesized samples were deployed for KET degradation. Results showed that Ag3PO4/P-g-C3N4 (1:1) exhibited the most excellent photocatalytic degradation performance on KET with a pseudo-first-order rate constant of 0.0326 min–1 at a neutral pH value, which was 3- and 6-fold faster than those of Ag3PO4 and P-g-C3N4, respectively. The elevated photocatalytic performance of Ag3PO4/P-g-C3N4 was attributed to the synergistic effects of the high charge separation capacity and Z-scheme heterojunction structure. Low concentrations of dissolved organic matter, nitrate, or bicarbonate accelerated KET degradation by Ag3PO4/P-g-C3N4, but high levels of these constituents would inhibit KET degradation. The scavenging experiments revealed that photogenerated superoxide radicals and holes were the main reactive species in the KET removal. A total of 12 degradation intermediates of KET over Ag3PO4/P-g-C3N4 were identified, and a possible degradation pathway was proposed. Demethylation, dehydrogenation, hydroxylation, deamination, ring opening, and sodium modification were the major pathways for KET degradation. Ag3PO4/P-g-C3N4 also exhibited a relatively good photocatalytic performance on KET degradation in surface water and a secondary effluent.
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