Simultaneous catalytic reduction of SO2 and NO from flue gas using H2S as a reductant at low temperatures

Literature Information

Publication Date 2020-01-15
DOI 10.1039/C9RE00347A
Impact Factor 4.239
Authors

Xianghong Lü, Hao Li, Xiaohui Du, Xue Wang, Minyi Lan, Jianlin Wu, Jin Zhu, Jianliang Sun, Feng Jiang


View Original

Abstract

Although harmful NO and SO2 in flue gas can be separately removed by established technologies, such as selective catalytic reduction (SCR) or selective non-catalytic reduction (SNCR) and a wet scrubbing process, an integrated method for simultaneous desulfurization and denitrification is still in demand and attractive to improve energy efficiency and reduce investment and operation costs. Upon this, a novel sulfur-cycling integrated technology (simultaneous catalytic desulfurization and denitrification with H2S (H2S-SCDD)) has been proposed and is considered to be a profitable solution for the flue gas treatment. However, a high operation temperature (over 600 °C) is required in the H2S-SCDD process for the sulfur-cycling flue gas treatment as reported. To realize the H2S-SCDD process at low temperatures, different catalysts were prepared and tested, such as Al2O3–TiO2 (AT) loaded with transition metal oxides. The results show that a CeO2-loaded AT catalyst (Ce–AT) was the suitable catalyst to balance NO and SO2 removal by the H2S-SCDD process in the temperature range of 300–400 °C. Increasing Ce loading on AT significantly increased the NO conversion but had a slightly negative effect on SO2 reduction. With 15% Ce loading on the AT catalyst (Ce15–AT), the optimal temperature for the H2S-SCDD process was 240–280 °C. While at 280 °C, the SO2 and NO conversions were about 75% and 90%, respectively, implying the efficient and simultaneous reduction of NO and SO2. Upon this, the sulfur-cycling process is promising and attractive for flue gas treatment in industrial sectors.

Related Literature

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

The nature of phase separation in a Ru–Sn–O ternary oxide electrocatalyst

Xin Wang, Fenyong Deng, Zhongzhi Tang, Bo Wu

2013-01-16 Paper

DOI: 10.1039/C3CP44528C

Organic ultra-thin film transistors with a liquid gate for extracellular stimulation and recording of electric activity of stem cell-derived neuronal networks

Tobias Cramer, Beatrice Chelli, Mauro Murgia, Marianna Barbalinardo, Eva Bystrenova, Dago M. de Leeuw, Fabio Biscarini

2013-01-16 Paper

DOI: 10.1039/C3CP44251A

Front cover

Cover

DOI: 10.1039/C3CP90018E

The fundamental chemical equation of aromaticity

2013-01-08 Paper

DOI: 10.1039/C2CP44075J

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

Hydrogen bonding network of truxenone on a graphite surface studied with scanning tunneling microscopy and theoretical computation

Zhi-Yong Yang, Yuan Tao, Ting Chen, Hui-Juan Yan, Zhi-Xiang Wang

2013-01-03 Paper

DOI: 10.1039/C2CP42828H

Thermoelectric power factor optimization in PEDOT:PSS tellurium nanowire hybrid composites

Arun Majumdar, Jeffrey J. Urban

2013-01-31 Paper

DOI: 10.1039/C3CP44558E

General treatment of the multimode Jahn–Teller effect: study of fullerenecations

Harry Ramanantoanina, Matija Zlatar, Pablo García-Fernández, Claude Daul

2012-11-22 Paper

DOI: 10.1039/C2CP43591H

Back cover

Cover

DOI: 10.1039/C2CP90217F

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.