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首页> 外文期刊>Applied Surface Science >Efficient visible-light photocatalytic degradation of imidacloprid and acetamiprid using a modified carbon nitride/tungstophosphoric acid composite induced by a nucleophilic addition reaction
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Efficient visible-light photocatalytic degradation of imidacloprid and acetamiprid using a modified carbon nitride/tungstophosphoric acid composite induced by a nucleophilic addition reaction

机译:用亲核加成反应诱导的改性碳氮化磷酸复合材料高效的可见光光催化降解吡虫啉和乙酰磷酸复合物

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摘要

This study proposed a novel method to combine modified carbon nitride (MCN) and tungstophosphoric acid (HPW). First, carbon nitride (CN), containing more uncondensed amino and carbonyl groups, was prepared by thermal condensation from urea at a low temperature. Then, in the presence of formic acid, a reversible nucleophilic addition reaction was performed between the carbonyl groups of formaldehyde (or CN) and amino groups of CN. Subsequently, during the HPW impregnation, the reverse reaction occurred, which increased the HPW loading. The results of the XPS and FTIR analyses verified the occurrence of a nucleophilic addition reaction during the formaldehyde treatment, as well as the formation of hydroxyl functional groups in the intermediate products. After impregnation with HPW, the disappearance of the hydroxyl groups and the recovery of the carbonyl groups were observed in the XPS Cls spectra. The as-prepared MCN450/HPW, obtained by modifying CN450 (CN calcined at 450 degrees C) with formaldehyde and loading with HPW, exhibited excellent visiblelight (lambda 400 nm) photocatalytic degradation of imidacloprid and acetamiprid. The degradation rate constant (0.70 h(-1)) of imidacloprid was 6.4 times that of CN450, while the degradation rate of acetamiprid by MCN450/ HPW was 11 times that of CN450. The results of the active species capture experiments showed that center dot OH and h(+) were the main active species in the visible-light photocatalytic degradation process.
机译:该研究提出了一种结合改性氮化碳(MCN)和钨磷酸(HPW)的新方法。首先,通过在低温下从尿素的热缩合来制备含有更多无抗体氨基和羰基的氮化物(CN)。然后,在甲酸存在下,在甲醛(或CN)的羰基和CN的氨基之间进行可逆的亲核加成反应。随后,在HPW浸渍期间,发生反应,增加了HPW负荷。 XPS和FTIR分析的结果验证了甲醛处理期间的亲核添加反应的发生,以及中间产物中的羟基官能团的形成。在用HPW浸渍后,在XPS CLS光谱中观察到羟基的消失和羰基的回收。通过将CN450(CN在450℃下煅烧)与甲醛和HPW加载的制备的MCN450 / HPW,表现出优异的咪酰啉代和乙酰哌啶的光催化降解的优异的粘性粘附性(Lambda> 400nm)光催化降解。吡虫啉的降解速率常数(0.70h(-1))为CN450的6.4倍,而MCN450 / HPW的acetamiprid的降解速率为CN450的11倍。活性物质捕获实验的结果表明,中心点OH和H(+)是可见光光催化降解过程中的主要活性物质。

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