Benzenecarboxylic acid production by oxidation of Shenmu char powders with aqueous sodium hypochlorite. (15th October 2020)
- Record Type:
- Journal Article
- Title:
- Benzenecarboxylic acid production by oxidation of Shenmu char powders with aqueous sodium hypochlorite. (15th October 2020)
- Main Title:
- Benzenecarboxylic acid production by oxidation of Shenmu char powders with aqueous sodium hypochlorite
- Authors:
- Lv, Jing-Hui
Wei, Xian-Yong
Zhang, Yang-Yang
Zong, Zhi-Min
Zhang, Yu-Long
Ma, Ming-Jie
Bai, Hong-Cun - Abstract:
- Graphical abstract: Highlights: Arenecarboxylic acids were produced in high yields by oxidizing SCPs with ASHC. The CAR structures in CPs suppress the formation of chlorine-substituted compounds. O2 − plays a crucial role in oxidizing ARs in SCPs to arenecarboxylic acids. Conjugation effect and electron-withdrawing effect affect the product distribution. Abstract: Char powders (CPs) are a promising feedstock for producing benzenecarboxylic acids (BCAs) due to their abundant condensed aromatic rings. An innovative exploration on the related mechanisms for oxidation and chlorination was attempted to guide the production of target BCAs in higher yields. The results declare that Shenmu CPs were converted to valuable BCAs in the yield of 16.2%. According to the product distribution, the total relative content (4.3%) of chlorine-substituted alkanoic acids (CSAAs) is much higher than that (0.2%) of alkanoic acids, while the result of chlorine-substituted BCAs is just the opposite and no chlorine-substituted arenecarboxylic acids with multiple aromatic rings (ARs) were produced. All the CSAAs have only short-chains. Carboxylic groups (CGs) tend to be chlorinated, but the steric effect of benzene ring leads to the inertness of most BCAs towards chlorination. The conjugation effect between CGs and ARs facilitates degrading condensed aromatics by stabilizing aryl radical intermediates. Thereby, the activity towards chlorination decreases with increasing the number of CGs, condensationGraphical abstract: Highlights: Arenecarboxylic acids were produced in high yields by oxidizing SCPs with ASHC. The CAR structures in CPs suppress the formation of chlorine-substituted compounds. O2 − plays a crucial role in oxidizing ARs in SCPs to arenecarboxylic acids. Conjugation effect and electron-withdrawing effect affect the product distribution. Abstract: Char powders (CPs) are a promising feedstock for producing benzenecarboxylic acids (BCAs) due to their abundant condensed aromatic rings. An innovative exploration on the related mechanisms for oxidation and chlorination was attempted to guide the production of target BCAs in higher yields. The results declare that Shenmu CPs were converted to valuable BCAs in the yield of 16.2%. According to the product distribution, the total relative content (4.3%) of chlorine-substituted alkanoic acids (CSAAs) is much higher than that (0.2%) of alkanoic acids, while the result of chlorine-substituted BCAs is just the opposite and no chlorine-substituted arenecarboxylic acids with multiple aromatic rings (ARs) were produced. All the CSAAs have only short-chains. Carboxylic groups (CGs) tend to be chlorinated, but the steric effect of benzene ring leads to the inertness of most BCAs towards chlorination. The conjugation effect between CGs and ARs facilitates degrading condensed aromatics by stabilizing aryl radical intermediates. Thereby, the activity towards chlorination decreases with increasing the number of CGs, condensation degree, and carbon numbers in the aliphatic chains. … (more)
- Is Part Of:
- Fuel. Volume 278(2020)
- Journal:
- Fuel
- Issue:
- Volume 278(2020)
- Issue Display:
- Volume 278, Issue 2020 (2020)
- Year:
- 2020
- Volume:
- 278
- Issue:
- 2020
- Issue Sort Value:
- 2020-0278-2020-0000
- Page Start:
- Page End:
- Publication Date:
- 2020-10-15
- Subjects:
- Char powders -- Aqueous sodium hypochlorite -- Oxidation -- Benzenecarboxylic acids
Fuel -- Periodicals
Coal -- Periodicals
Coal
Fuel
Periodicals
662.6 - Journal URLs:
- http://www.sciencedirect.com/science/journal/latest/00162361 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.fuel.2020.118194 ↗
- Languages:
- English
- ISSNs:
- 0016-2361
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4048.000000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 13553.xml