氧化石墨烯量子点活化过氧乙酸在大肠杆菌灭活和LED反应器光去除有机染料中的协同作用

C. Tshangana, A. Muleja, A. Kuvarega, B. Mamba
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引用次数: 6

摘要

摘要:本研究提出了一种低影响的工艺,利用过氧乙酸(PAA)和氧化石墨烯量子量子量子点的协同作用来降解生物降解性差的有机化合物,并有可能在废水处理中取代氯化。研究了GQDs在GQDs/PAA活性中的作用以及GQDs负载的影响。结果表明,在GQDs/PAA体系中,增加GQDs的负载可大大提高其光降解效率。相反,由于可用的活性位点较少,增加PAA浓度会略微提高效率。GQDs作为催化剂,自由基清除实验证实,降解是通过生成羟基(•OH)和过氧(CH3C(=O)OO•)自由基进行的。基于HPLC-MS检测的反应副产物,提出了有机染料降解的可能机理。通过扫描显微镜观察大肠杆菌的形态变化,阐明了大肠杆菌灭活的机制。提出的抗菌机制包括PAA最初通过细胞膜扩散,造成细胞损伤和细胞物质渗漏,导致细胞死亡。细菌再生研究证实,GQDs/PAA能够绕过微生物修复DNA损伤的自然机制。
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The synergistic effect of peracetic acid activated by graphene oxide quantum dots in the inactivation of E. coli and organic dye removal with LED reactor light
Abstract This study presents a low-impact process that uses the synergy of peracetic acid (PAA) and graphene oxide quantum GQDs to degrade poorly biodegradable organic compounds and potentially substitute chlorination in wastewater treatment. The role of GQDs in GQDs/PAA activity and the effect of GQDs loading were examined. The results showed that increasing GQDs loading in the GQDs/PAA system greatly improved the photodegradation efficiency. Conversely, increasing the PAA concentration slightly enhanced efficiency due to few active sites being available. GQDs acted as catalysts and radical scavenging experiments confirmed that the degradation occurred via generation of hydroxyl (•OH) and peroxy (CH3C(=O)OO•)) radicals. A probable degradation mechanism of the organic dye was presented based on the reaction by-products detected after HPLC-MS studies. The E. coli inactivation mechanism was elucidated by monitoring the morphological changes of E. coli using scanning microscopy. The proposed antimicrobial mechanism includes the initial diffusion of PAA through the cell membrane which caused damage and induced cellular matter leakage, resulting in cell death. Bacterial regrowth studies confirmed GQDs/PAA were able to bypass the natural mechanisms of microorganisms that enables them to repair any damages in their DNA.
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