Controversial mechanism of simultaneous photocatalysis and Fenton-based processes: additional effect or synergy?
文献信息
Olivier Monfort, Arshitha Madhusudhan, Martin Motola
Many published articles have reported the advantages of coupling photocatalysis and Fenton-based processes for environmental remediation purposes, especially wastewaters treatment, but without providing detailed discussion on how and why the resulting process is better, thus leading to misconception about their synergy. In this work, the context of the water pollution is presented along with the pros and cons of individual photocatalysis and Fenton-based processes. The simultaneous triggering of these two advanced oxidation processes is critically discussed from both performance and mechanism sides since additional effect and synergy are often misunderstood in the literature. Insights into research approaches to clarify the synergistic mechanism between photocatalysis and Fenton-based processes are also provided. One of the key features is to assess the separated contribution of the individual processes and also to elucidate the charge carriers’ dynamics at the surface of the catalyst. The aim of this work is to inform scientists about the complexity of simultaneously triggered photocatalysis and Fenton-based processes but also to highlight the potential development of a new generation of catalysts that might be integrated to current wastewater treatment technology to achieve higher efficiency and their implications in the circular economy of water.
相关文献
SAR study of 4-arylazo-3,5-diamino-1H-pyrazoles: identification of small molecules that induce dispersal of Pseudomonas aeruginosa biofilms
Charlotte U. Jansen, Jesper Uhd, Jens B. Andersen, Louise D. Hultqvist, Tim H. Jakobsen, Martin Nilsson, Michael Givskov, Tim Tolker-Nielsen, Katrine M. Qvortrup
DOI: 10.1039/D1MD00275A
Sulfonium-based liposome-encapsulated antibiotics deliver a synergistic antibacterial activity
Anjali Patel, Subhasis Dey, Kamal Shokeen, Tomasz M. Karpiński, Senthilkumar Sivaprakasam, Sachin Kumar
DOI: 10.1039/D1MD00091H
Macrocyclic peptides that inhibit Wnt signalling via interaction with Wnt3a
Manuel E. Otero-Ramirez, Kyoko Matoba, Emiko Mihara, Junichi Takagi, Hiroaki Suga
DOI: 10.1039/D0CB00016G
Second-generation tricyclic pyrimido-pyrrolo-oxazine mTOR inhibitor with predicted blood–brain barrier permeability
Chiara Borsari, Erhan Keles, Andrea Treyer, Martina De Pascale, Matthias Hamburger, Matthias P. Wymann
DOI: 10.1039/D0MD00408A
Virtual screening and in vitro validation identifies the first reported inhibitors of Salmonella enterica HPPK
Ronel Müller, Tiaan M. Gerwel, Magambo Phillip Kimuda, Özlem Tastan Bishop, Clinton G. L. Veale, Heinrich C. Hoppe
DOI: 10.1039/D1MD00237F
Synthesis and evaluation of pyridine-derived bedaquiline analogues containing modifications at the A-ring subunit
Lisa Barbaro, Gayathri Nagalingam, James A. Triccas, Jonathan B. Baell, Daniel L. Priebbenow
DOI: 10.1039/D1MD00063B
Challenges and opportunities of pharmaceutical cocrystals: a focused review on non-steroidal anti-inflammatory drugs
Utsav Garg, Yasser Azim
DOI: 10.1039/D0MD00400F
Design, synthesis, crystal structure and anti-plasmodial evaluation of tetrahydrobenzo[4,5]thieno[2,3-d]pyrimidine derivatives
Kavita Pal, Md Kausar Raza, Jenny Legac, Md. Ataur Rahman, Shoaib Manzoor, Philip J. Rosenthal, Nasimul Hoda
DOI: 10.1039/D1MD00038A
Using NMR to identify binding regions for N and C-terminal Hsp90 inhibitors using Hsp90 domains
Jeanette R. McConnell, H. Jane Dyson, Shelli R. McAlpine
DOI: 10.1039/D0MD00387E
您可能还喜欢
什么是2-氨基戊烷(CAS号:63493-28-7)?
2-氨基戊烷,又名pentan-2-amine,是一种有机化合物,分子式为C5H11NH2。它是一种无色透明液体,有氨味。该化合物在工业和研究中有一定的应用。
反式-4-[4-[[[5-[(3,4-二氟苯基)氨基]-1,3,4-恶二唑-2-基]羰基]氨基]苯基]环己烷乙酸(CAS号:892489-52-0)的物理化学性质是什么?
该化合物为白色固体,分子量为552.31 g/mol。它在水中溶解度较低,在有机溶剂如乙腈、乙酸乙酯中有较好的溶解性。该化合物具有较高的化学稳定性,对酸和碱具有...
如何处理含有Pyrotinib dimaleate(CAS号:1397922-61-0)的废料?
处理含有Pyrotinib dimaleate 的废料时,应遵循当地的法规要求。首先,收集废料并进行分类,确保没有与其他化学品混合。然后,采取适当的物理和化学处...
在合成中是否有4-(5-5-乙基-1,2,4-噁二唑-3-基)苯甲酸乙酯(CAS号:1166756-79-1)的替代品?
在合成过程中,可以考虑使用其他结构类似的化合物作为替代品,例如苯甲酸酯类化合物,如2-乙基-5-甲基噁二唑基苯甲酸乙酯等。这些替代品可能具有相似的化学性质,但在...
如何处理含有1-((叔丁氧基羰基)氨基)环丁烷甲酸甲酯(CAS号:880166-10-9)的废料?
处理含有该化合物的废液时,应先确保其完全反应并转化为无害物质。对于未反应的化合物,建议采用中和处理后进行蒸馏回收,剩余物可使用化学氧化法或焚烧法进行无害化处理。...
2-({[3,5-二(三氟甲基)苯基]磺酰基}氨基)-4-(甲基硫代)丁酸甲酯(CAS号:175202-21-8)的市场或研究趋势如何?
目前该化合物主要应用于药物合成领域,尤其在开发新型抗癌药物方面具有潜在应用。随着制药行业的持续发展,对于高效、低毒的合成中间体需求增加,预计该化合物的研究和应用...
N,N-乙烯双(碘乙酰胺)(CAS号:7250-43-3)的物理化学性质是什么?
N,N-乙烯双(碘乙酰胺)是一种白色或类白色固体,易溶于乙醇、丙酮等有机溶剂,但在水中溶解度较低。该化合物具有较高的反应活性,可以与其他含有活性氢的化合物发生酰...
7-Fluoro-1H-spiro[furo[3,4-c]pyridine-3,4'-piperidine](CAS号:1283090-73-2)通常如何合成?
该化合物可以通过环合反应合成,首先合成吡啶和哌啶的衍生物,然后在合适的条件下进行环合反应得到目标化合物。常用的催化剂包括某些金属盐类,产率一般在70%-90%之...
处理3-乙酰滇乌碱(CAS号:80787-51-5)时应注意哪些实验室安全事项?
在处理3-乙酰滇乌碱时,应穿戴适当的个人防护装备(PPE),如实验服、手套(丁腈手套或PVC手套)、护目镜和口罩。实验应在通风橱中进行,以减少吸入或皮肤接触的风...
如何储存2-溴-5-硝基-4-羧酸(CAS号:1053655-82-5)?
2-溴-5-硝基-4-羧酸应存放在阴凉、干燥、通风良好的地方,远离火源和热源。避免与还原剂、碱性物质接触。储存容器应密封,防止吸湿。
来源期刊
Chemical Communications

ChemComm publishes urgent research which is of outstanding significance and interest to experts in the field, while also appealing to the journal’s broad chemistry readership. Our communication format is ideally suited to short, urgent studies that are of such importance that they require accelerated publication. Our scope covers all topics in chemistry, and research at the interface of chemistry and other disciplines (such as materials science, nanoscience, physics, engineering and biology) where there is a significant novelty in the chemistry aspects. Major topic areas covered include: Analytical Chemistry Catalysis Chemical Biology and medicinal chemistry Computational Chemistry and Machine Learning Energy and sustainable chemistry Environmental Chemistry Green Chemistry Inorganic Chemistry Materials Chemistry Nanoscience Organic Chemistry Physical Chemistry Polymer Chemistry Supramolecular Chemistry











![4-{[4-(Trifluoromethoxy)benzyl]oxy}benzonitrile structure 4-{[4-(Trifluoromethoxy)benzyl]oxy}benzonitrile structure](https://cnstatic.chemtradehub.com/structs/103/1036629-63-6-2172.webp)
-1,2-cyclohexanediamine structure N,N'-Bis[3-(2-methoxyphenyl)-2-hydroxybenzyl](1R,2R)-1,2-cyclohexanediamine structure](https://cnstatic.chemtradehub.com/structs/928/928769-12-4-a4f0.webp)

