Reaction-volume dependent chemistry of highly selective photocatalytic reduction of nitrobenzene

Literature Information

Publication Date 2019-08-02
DOI 10.1039/C9RE00251K
Impact Factor 4.239
Authors

Seungwook Jang, Bum-Joon Jung, Mi-Jeong Kim, Dong-Pyo Kim


View Original

Abstract

Reaction-volume dependent photocatalytic reduction of nitrobenzene was investigated in various batch reactors and continuous-flow microreactors (CFMs) with different surface area to volume ratios (SA/V) under visible-light irradiation, leading to control of the photochemical reduction route, reaction speed and product selectivity. A batch reactor with less than 1.5 cm−1 SA/V ratio produced only aniline in 96% selectivity with 40% conversion by a direct reaction route. In contrast, the CFM with an 80 cm−1 SA/V ratio showed production of high-value azoxybenzene in 99% selectivity with 99% conversion through a condensation reaction route. In particular, a parylene thin film microreactor with a 100 μm channel height (400 cm−1 SA/V ratio) achieved perfect conversion and selectivity to azoxybenzene within only 50 min of reaction, compared to 20 h of reaction in the batch reactor to produce aniline. The mechanistic reaction progress was monitored by conducting time-dependent reactions of nitrobenzene and nitrosobenzene. Furthermore, the photocatalysis of various nitro-aromatic compounds also exhibited the identical reaction-volume dependent chemistry with excellent product selectivity.

Related Literature

Cage lifetimes of ionic liquids as studied by the magnetic field effect probe

Tomohide Okada, Tomoaki Yago, Tadashi Takamasu, Masanobu Wakasa

2012-01-17 Paper

DOI: 10.1039/C2CP23747D

Photoinduced ultrafast dynamics of the triphenylamine-based organic sensitizer D35 on TiO2, ZrO2 and in acetonitrile

Kawon Oum, Peter W. Lohse, Johannes R. Klein, Oliver Flender, Mirko Scholz, Anders Hagfeldt, Gerrit Boschloo, Thomas Lenzer

2013-02-12 Paper

DOI: 10.1039/C3CP44095H

The fundamental chemical equation of aromaticity

2013-01-08 Paper

DOI: 10.1039/C2CP44075J

Fabrication and photoelectrochemical properties of ZnS/Au/TiO2nanotube array films

Yan-Feng Zhu, Juan Zhang, Lu Xu, Ya Guo, Xiao-Ping Wang, Rong-Gui Du, Chang-Jian Lin

2013-01-22 Paper

DOI: 10.1039/C3CP43572E

Polyallylamine-directed green synthesis of platinum nanocubes. Shape and electronic effect codependent enhanced electrocatalytic activity

Gengtao Fu, Ke Wu, Xian Jiang, Lin Tao, Yu Chen, Jun Lin, Yiming Zhou, Shaohua Wei, Yawen Tang, Tianhong Lu, Xinghua Xia

2013-01-10 Paper

DOI: 10.1039/C3CP44191A

Probing the balance of attraction and repulsion in binary mixtures of dimethyl sulfoxide and n-alcohols

Andrew Ellis, Florian M. Zehentbauer

2012-11-30 Communication

DOI: 10.1039/C2CP42902K

Hydrophobic and polar ionic liquids

2013-01-23 Paper

DOI: 10.1039/C3CP44214D

Plasma electrochemistry: voltammetry in a flame plasma electrolyte

Atif Elahi, Daren J. Caruana

2012-11-20 Paper

DOI: 10.1039/C2CP43431H

Mutual diffusion in the ternary mixture of water + methanol + ethanol and its binary subsystems

Stanislav Pa, Gabriela Guevara-Carrion, Hans Hasse, Jadran Vrabec

2013-01-10 Paper

DOI: 10.1039/C3CP43785J

Access to enhanced differences in Marcus–Hush and Butler–Volmer electron transfer theories by systematic analysis of higher order AC harmonics

Gareth P. Stevenson, Ruth E. Baker, Gareth F. Kennedy, Alan M. Bond, David J. Gavaghan, Kathryn Gillow

2012-11-12 Paper

DOI: 10.1039/C2CP43193A

You might also like

Compound Q&A

What is 3-Fluoro-2-methylbenzylamine (CAS: 771573-36-5)?

3-Fluoro-2-methylbenzylamine is an organic compound with the CAS number 771573-3...

771573-36-53-Fluoro-2-methylben...
Compound Q&A

Is Tert-butyl 2-(oxetan-3-ylidene)acetate (CAS: 1207175-03-8) safe?

Tert-butyl 2-(oxetan-3-ylidene)acetate is considered safe for its intended uses ...

1207175-03-8Tert-butyl 2-(oxetan...
Compound Q&A

What precautions should be taken when handling 4-Acetyl-2-fluorobenzonitrile (CAS: 214760-18-6)?

Proper personal protective equipment (PPE) such as gloves, goggles, and a lab co...

214760-18-64-Acetyl-2-fluoroben...
Compound Q&A

How is 2-Ethyl-4-methyl-1,3-thiazole (CAS: 15679-12-6) typically synthesized?

2-Ethyl-4-methyl-1,3-thiazole is commonly synthesized via the reaction of thiour...

15679-12-62-Ethyl-4-methyl-1,3...
Compound Q&A

How should 5',5''-([2,2'-Bithiophene]-5,5'-diyl)bis(([1,1':3',1''-terphenyl]-4,4''-dicarboxylic acid)) (CAS: 1227780-71-3) be stored?

This compound should be stored in a cool, dry place away from direct sunlight an...

1227780-71-35',5''''-([2,2'-Bith...
Compound Q&A

What regulatory guidelines apply to L-Lysine Acetate Salt (CAS: 52315-92-1)?

L-Lysine Acetate Salt (CAS: 52315-92-1) is subject to various regulatory guideli...

52315-92-1L-LYSINE ACETATE SAL...
Compound Q&A

Is 6-Fluoro-3-hydroxy-2-pyrazinecarboxamide (CAS: 259793-96-9) safe?

6-Fluoro-3-hydroxy-2-pyrazinecarboxamide (CAS: 259793-96-9) is generally conside...

259793-96-96-Fluoro-3-hydroxy-2...
Compound Q&A

What are the physical and chemical properties of 1,1'-Sulfonylbis(1H-imidazole) (CAS: 7189-69-7)?

1,1'-Sulfonylbis(1H-imidazole) is a crystalline solid with a molecular weight of...

7189-69-71,1'-Sulfonylbis(1H-...
Compound Q&A

What industries use 4-methyl-7-nitro-1H-indole-3-carbonitrile (CAS: 289483-82-5)?

4-Methyl-7-nitro-1H-indole-3-carbonitrile (CAS: 289483-82-5) is primarily used i...

289483-82-54-methyl-7-nitro-1H-...
Compound Q&A

How should waste containing 5-Bromo-3-indolyl-beta-galactoside (CAS: 97753-82-7) be handled?

Waste containing 5-Bromo-3-indolyl-beta-galactoside (CAS: 97753-82-7) should be ...

97753-82-75-Bromo-3-indolyl-be...

Source Journal

Reaction Chemistry & Engineering

Reaction Chemistry & Engineering
CiteScore: 0
Self-citation Rate: 8.8%
Articles per Year: 284

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.

Recommended Compounds

Recommended Suppliers

Disclaimer
This page provides academic journal information for reference and research purposes only. We are not affiliated with any journal publishers and do not handle publication submissions. For publication-related inquiries, please contact the respective journal publishers directly.
If you notice any inaccuracies in the information displayed, please contact us at support@chemtradehub.com. We will promptly review and address your concerns.