Electro-catalytic membrane reactors for the degradation of organic pollutants – a review
文献情報
Marc Cretin, Lingxue Kong, Luke A. O'Dell, Andrea Merenda
The occurrence and accumulation of persistent organic pollutants (POPs) in wastewater represent global challenges since they are bio-refractory pollutants, which cannot be remediated with classical wastewater treatment systems. Amongst emerging technologies, POPs may be treated by electrochemical advanced oxidation processes to remediate selective contaminants through specific degradation pathways. Although dense anodic electrodes have been extensively employed in such electrochemical processes, the surface and bulk properties of such electrodes limit the mass transfer and degradation rates of these pollutants, opening the route to the application of porous electrode materials, referred to as electro-catalytic membrane reactors (ECMRs). The application of ECMRs facilitates the degradation of these compounds, while also simultaneously allowing for fine filtration operation. This paper is focussed on discussing the recent development and preparative methods of anodic membranes, and the catalytic performance of these membranes for degradation of organics in wastewater. The effect of physicochemical characteristics such as the surface area, porosity, and morphology on the catalytic performance of the membranes is elaborated. A summary of the most relevant electro-catalytic membrane materials and parameters, which contribute to the electrocatalytic process optimisation, is presented, to investigate the impact of the material properties on the catalytic rate of the reaction for efficient output. Therefore, this aims at critically assessing the properties of electrocatalytic membranes used in ECMR, mechanisms involved in degradation of organic pollutants and optimal parameters to carry out electrocatalytic reactions, which helps in identifying and bridging the research gaps for the large scale employment of ECMRs in wastewater remediation.
おすすめジャーナル

Medicinal Chemistry Research

Bioorganic & Medicinal Chemistry Letters

Biocatalysis and Biotransformation

Polycyclic Aromatic Compounds

Journal of Chemical Sciences

Critical Reviews in Solid State and Materials Sciences

Acta Metallurgica Sinica-English Letters

Herald of the Russian Academy of Sciences

Main Group Chemistry

Atomization and Sprays
関連文献
Highly efficient quenching of excimer fluorescence by perylene diimide in DNA
Nicolas Bouquin, Vladimir L. Malinovskii, Robert Häner
DOI: 10.1039/B802193G
Improved 3D DOSY-TOCSY experiment for mixture analysis
Stéphane Viel, Stefano Caldarelli
DOI: 10.1039/B802789G
A mechanistic study on the oxidation of hydrazides: application to the tuberculosis drug isoniazid‡
Ruth I. J. Amos, Brendon S. Gourlay, Brian F. Yates
DOI: 10.1039/B719570B
Interpenetrating single helical capsules
Emanuela Berni, Joachim Garric, Corinne Lamit, Brice Kauffmann, Jean-Michel Léger, Ivan Huc
DOI: 10.1039/B719712H
Rational design of supramolecular chirality in porphyrin assemblies: the halogen bond case‡
Sankar Muniappan, Sophia Lipstman, Israel Goldberg
DOI: 10.1039/B719625C
Unimolecular binary half-adders with orthogonal chemical inputs
Lu Zhang, Wesley A. Whitfield, Lei Zhu
DOI: 10.1039/B719644J
Preparation of silyl substituted crotylzinc reagents and their highly diastereoselectiveaddition to carbonyl compounds
Matthew D. Helm, Peter Mayer, Paul Knochel
DOI: 10.1039/B802157K
Chemical modifications of AFM tips for the study of molecular recognition events
Régis Barattin, Normand Voyer
DOI: 10.1039/B614328H
Clean and efficient synthesis of O-silylcarbamates and ureas in supercritical carbon dioxide
Matthew J. Fuchter, Catherine J. Smith, Alistair Boyer, Simon Saubern, John H. Ryan, Andrew B. Holmes
DOI: 10.1039/B801537F
こちらもおすすめ
3-イチチルビフェニルはどのように合成されますか?
3-イチチルビフェニルは、ビフェニルとイチプロピオニトリルを回収率約90%で反応させて合成されます。触媒は通常、亜リチウムホウ素を用います。
8-溴-5-三氟甲基喹啉はどのように合成されますか?
8-溴-5-三氟甲基喹啉は、5-トリフルオロメチル-2-メチル-1,3-ベンゼンジオールをブロモエタノールと反応させて生成します。この反応は塩基性条件下で行われ...
ジメチル4-(4,4,5,5-テトラメチル-1,3,2-ドioxaborolan-2-基)-2,6-ピリジンジカルボイル酸フェニルアミニドの代替品はありますか?
ジメチル4-(4,4,5,5-テトラメチル-1,3,2-ドioxaborolan-2-基)-2,6-ピリジンジカルボイル酸フェニルアミニドの代替品としては、4-...
N-(3,5-ヘキサクロロ-4-ピリドインイル)-8-メチオキシ-5-キノリンカーボン酸の市場動向や研究トレンドはどのようなものでしょうか?
N-(3,5-ヘキサクロロ-4-ピリドインイル)-8-メチオキシ-5-キノリンカーボン酸の市場動向は、主に産業用途での需要により影響を受けます。研究トレンドとし...
イソステアロイルグリセリルは安全ですか?
イソステアロイルグリセリルは一般的に安全性が高いとされていますが、過度な使用や個人差により皮�owsん炎などの反応が起こる可能性があります。使用前に医師に相談す...
1-(二苯甲基)-3,3-二氟-氮杂环丁烷の市場動向や研究トレンドはどうですか?
1-(二苯甲基)-3,3-二氟-氮杂环丁烷の市場動向は、医薬品や合成化学の研究分野で注目を集めています。新興研究は、該当化合物の合成改良と生体内での作用メカニズ...
3-チオフェンスチオールの物理化学的性質は何ですか?
3-チオフェンスチオールのCAS番号は7774-73-4です。結晶性の白色粉末で、分子量は122.17です。この化合物は水に微溶解し、エタノールやジクロロメタン...
2-Methyl-2-propanyl (2S)-2-(aminomethyl)-1-piperidinecarboxylateは安全ですか?
2-Methyl-2-propanyl (2S)-2-(aminomethyl)-1-piperidinecarboxylateは一定の安全性基準を満たしていま...
CAS番号1316822-90-8の化合物は安全ですか?
CAS番号1316822-90-8の化合物は安全性に関しては評価が不足していますが、一般的には生物学的に活性な物質であり、取り扱いには適切な安全防護措置が必要で...
Tert-butyl 2-(2-羟基乙基)哌嗪-1-羧酸はどのように保存すればよいですか?
Tert-butyl 2-(2-羟基乙基)哌嗪-1-羧酸は、冷暗所で保存し、直射日光から遠ざけてください。容器は密閉し、高湿度や高温を避けて保管してください。
掲載誌
Reaction Chemistry & Engineering

Reaction Chemistry & Engineering is an interdisciplinary journal reporting cutting-edge research focused on enhancing the understanding and efficiency of reactions. Reaction engineering leverages the interface where fundamental molecular chemistry meets chemical engineering and technology. Challenges in chemistry can be overcome by the application of new technologies, while engineers may find improved solutions for process development from the latest developments in reaction chemistry. Reaction Chemistry & Engineering is a unique forum for researchers whose interests span the broad areas of chemical engineering and chemical sciences to come together in solving problems of importance to wider society. All papers should be written to be approachable by readers across the engineering and chemical sciences. Papers that consider multiple scales, from the laboratory up to and including plant scale, are particularly encouraged.
![1-(1-Benzyl-1,2,3,6-tetrahydropyridin-4-yl)-1H-benzo[d]imidazol-2(3H)-one structure 1-(1-Benzyl-1,2,3,6-tetrahydropyridin-4-yl)-1H-benzo[d]imidazol-2(3H)-one structure](https://static.chemtradehub.com/structs/603/60373-71-9-7dfb.webp)
![5'-Fluoro-[2,3'-biindolinylidene]-2',3-dione structure 5'-Fluoro-[2,3'-biindolinylidene]-2',3-dione structure](https://static.chemtradehub.com/structs/251/251903-00-1-9cb1.webp)
![N-{[(2-Methyl-2-propanyl)oxy]carbonyl}-L-methionylglycine structure N-{[(2-Methyl-2-propanyl)oxy]carbonyl}-L-methionylglycine structure](https://static.chemtradehub.com/structs/234/23446-03-9-e1e5.webp)

