Jing Zhang
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Jing Zhang has a total of 68 co-authors. Here are the top co-authors by number of shared publications:
Jun Ma
School of Environment, Harbin Institute of Technology, Harbin, 150090, China
7 shared publications- Timothy J. Strathmann
Colorado School of Mines
6 shared publications Zhenyu Shi
Environment Monitoring Center of Jiangsu Province, Nanjing 210036, P. R. China
6 shared publicationsTimothy J. Strathmann
Colorado Sch Mines, Dept Civil & Environm Engn, 1500 Illinois St, Golden, CO 80401 USA
5 shared publicationsDingxiang Wang
School of Environment, Harbin Institute of Technology, Harbin, 150090, China; Department of Civil and Environmental Engineering, The Hong Kong University of Science and Technology, Hong Kong, China
4 shared publications- Dingxiang Wang
Shenyang Institute of Engineering
4 shared publications
Latest Publications
- Open Access
- 28 November 2025
- Published by Royal Society of Chemistry (RSC) in Green Chemistry
- Vol. 28 (5) , 2166-2195
From lignin to jet fuel: advancing selective cyclohydrocarbon production toward full compatibility with aviation standards
Assessing lignin-derived cycloalkane-rich fuels produced via depolymerization and hydrodeoxygenation as drop-in jet fuels, focusing on process intensification, aviation fuel standards, and environmental and economic sustainability.
- 28 November 2025
- Published by Royal Society of Chemistry (RSC) in Green Chemistry
- Vol. 28 (5) , 2166-2195
Open AccessFrom lignin to jet fuel: advancing selective cyclohydrocarbon production toward full compatibility with aviation standards
Assessing lignin-derived cycloalkane-rich fuels produced via depolymerization and hydrodeoxygenation as drop-in jet fuels, focusing on process intensification, aviation fuel standards, and environmental and economic sustainability.
- Open Access
- 21 August 2025
- Published by Springer Nature in Nature Communications
- Vol. 16 (1) , 1-11
CO-promoted polyethylene hydrogenolysis with renewable formic acid as hydrogen donor
Hydrogenolysis has emerged as a promising strategy for the chemical recycling of plastic waste, yet its reliance on high-pressure hydrogen poses significant challenges. Biomass- or CO2-derived formic acid (FA) is a renewable hydrogen carrier with the advantages of low toxicity and ease of storage and transport. Here, we use FA to replace high-pressure hydrogen to convert polyethylene (PE) into fuels and chemicals with only 4.1% gaseous products by a RuPt alloy catalyst. We demonstrate that the trace amounts of CO generated from the decomposition of FA do not poison the active sites, but rather induce the formation of Ruδ+, which facilitates the C–C bond cleavage during PE hydrogenolysis. This approach eliminates the need for high-pressure hydrogen and provides a more flexible and adaptable approach for decentralized plastic processing.
- 21 August 2025
- Published by Springer Nature in Nature Communications
- Vol. 16 (1) , 1-11
Open AccessCO-promoted polyethylene hydrogenolysis with renewable formic acid as hydrogen donor
Hydrogenolysis has emerged as a promising strategy for the chemical recycling of plastic waste, yet its reliance on high-pressure hydrogen poses significant challenges. Biomass- or CO2-derived formic acid (FA) is a renewable hydrogen carrier with the advantages of low toxicity and ease of storage and transport. Here, we use FA to replace high-pressure hydrogen to convert polyethylene (PE) into fuels and chemicals with only 4.1% gaseous products by a RuPt alloy catalyst. We demonstrate that the trace amounts of CO generated from the decomposition of FA do not poison the active sites, but rather induce the formation of Ruδ+, which facilitates the C–C bond cleavage during PE hydrogenolysis. This approach eliminates the need for high-pressure hydrogen and provides a more flexible and adaptable approach for decentralized plastic processing.
- 2 July 2024
- Published by Elsevier in Chemosphere
- Vol. 362, 142752
Homogeneous to heterogeneous redox mediator enhancing ferrate(VI) oxidation of sulfamethoxazole: Role of ferrate(VI) activation and electron shuttle
- 2 July 2024
- Published by Elsevier in Chemosphere
- Vol. 362, 142752
Homogeneous to heterogeneous redox mediator enhancing ferrate(VI) oxidation of sulfamethoxazole: Role of ferrate(VI) activation and electron shuttle
- 27 April 2024
- Published by Elsevier in Journal of Hazardous Materials
- Vol. 471, 134432
Vacuum-ultraviolet based advanced oxidation and reduction processes for water treatment
- 27 April 2024
- Published by Elsevier in Journal of Hazardous Materials
- Vol. 471, 134432
Vacuum-ultraviolet based advanced oxidation and reduction processes for water treatment
- Open Access
- 20 April 2024
- Published by Elsevier in Environmental Science and Ecotechnology
- Vol. 21, 100421
Overlooked interaction between redox-mediator and bisphenol-A in permanganate oxidation
- 20 April 2024
- Published by Elsevier in Environmental Science and Ecotechnology
- Vol. 21, 100421
Open AccessOverlooked interaction between redox-mediator and bisphenol-A in permanganate oxidation
- 7 December 2023
- Published by Elsevier in Chemosphere
- Vol. 349, 140875
Highly efficient reduction of bromate by vacuum UV/sulfite system
- 7 December 2023
- Published by Elsevier in Chemosphere
- Vol. 349, 140875
Highly efficient reduction of bromate by vacuum UV/sulfite system
- 20 October 2023
- Published by Elsevier in Water Research
- Vol. 247, 120768
Understanding molecular-level reactions between permanganate/ferrate and dissolved effluent organic matter from municipal secondary effluent
- 20 October 2023
- Published by Elsevier in Water Research
- Vol. 247, 120768
Understanding molecular-level reactions between permanganate/ferrate and dissolved effluent organic matter from municipal secondary effluent
- 29 September 2023
- Published by Elsevier in Journal of Hazardous Materials
- Vol. 462, 132659
Comprehending the practical implementation of permanganate and ferrate for water remediation in complex water matrices
- 29 September 2023
- Published by Elsevier in Journal of Hazardous Materials
- Vol. 462, 132659
Comprehending the practical implementation of permanganate and ferrate for water remediation in complex water matrices
- 18 August 2023
- Published by Elsevier in Water Research
- Vol. 244, 120500
PTIO as a redox mediator to enhance organic contaminants oxidation by permanganate
- 18 August 2023
- Published by Elsevier in Water Research
- Vol. 244, 120500
PTIO as a redox mediator to enhance organic contaminants oxidation by permanganate
- 24 May 2023
- Published by American Chemical Society (ACS) in ACS Omega
- Vol. 8 (22) , 19969-19975
Catalytic Hydrothermal Deoxygenation of Stearic Acid with Ru/C: Effects of Alcohol- and Carboxylic Acid-Based Hydrogen Donors
Catalytic hydrothermal processing is a promising technology for the production of biofuels used in transportation to alleviate the energy crisis. An important challenge for these processes is the need for an external supply of hydrogen gas to accelerate the deoxygenation of fatty acids or lipids. It follows that in situ-produced hydrogen can improve process economics. This study reports on the use of various alcohol and carboxylic acid amendments as sources for in situ hydrogen production to accelerate Ru/C-catalyzed hydrothermal deoxygenation of stearic acid. Addition of these amendments significantly increases yields of liquid hydrocarbon products, including the major product heptadecane, from stearic acid conversion at subcritical conditions (330 °C, 14-16 MPa during the reaction). This research provided guidance for simplifying the catalytic hydrothermal process of biofuel production, making the production of the desired biofuel in one pot possible without the need for an external H2 supply.
- 24 May 2023
- Published by American Chemical Society (ACS) in ACS Omega
- Vol. 8 (22) , 19969-19975
Catalytic Hydrothermal Deoxygenation of Stearic Acid with Ru/C: Effects of Alcohol- and Carboxylic Acid-Based Hydrogen Donors
Catalytic hydrothermal processing is a promising technology for the production of biofuels used in transportation to alleviate the energy crisis. An important challenge for these processes is the need for an external supply of hydrogen gas to accelerate the deoxygenation of fatty acids or lipids. It follows that in situ-produced hydrogen can improve process economics. This study reports on the use of various alcohol and carboxylic acid amendments as sources for in situ hydrogen production to accelerate Ru/C-catalyzed hydrothermal deoxygenation of stearic acid. Addition of these amendments significantly increases yields of liquid hydrocarbon products, including the major product heptadecane, from stearic acid conversion at subcritical conditions (330 °C, 14-16 MPa during the reaction). This research provided guidance for simplifying the catalytic hydrothermal process of biofuel production, making the production of the desired biofuel in one pot possible without the need for an external H2 supply.