Huiling Fan
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Research Interests
Huiling Fan has a total of 92 co-authors. Here are the top co-authors by number of shared publications:
Chao Yang
17 shared publicationsJu Shangguan
State Key Laboratory of Clean and Efficient Coal Utilization, Taiyuan University of Technology, Taiyuan 030024, China
11 shared publicationsJian Wang
State Key Laboratory of Coal Science and Technology, Co-Founded By Shanxi Province and the Ministry of Science and Technology, Taiyuan University of Technology, Taiyuan, China
6 shared publications- Jie Mi
Key Laboratory of Coal Science and Technology of Shanxi Province and Ministry of Education, Taiyuan University of Technology, Taiyuan 030024, China
5 shared publications Yeshuang Wang
State Key Laboratory of Clean and Efficient Coal Utilization
5 shared publicationsZhen Tian
5 shared publications
Latest Publications
- 29 May 2025
- Published by Elsevier in Aquatic Toxicology
- Vol. 286, 107431
Environmental electron shuttle impacting nano-bio interactions via bio-activity-dependent mechanism
- 29 May 2025
- Published by Elsevier in Aquatic Toxicology
- Vol. 286, 107431
Environmental electron shuttle impacting nano-bio interactions via bio-activity-dependent mechanism
- 18 January 2025
- Published by American Chemical Society (ACS) in Inorganic Chemistry
- Vol. 64 (4) , 2106-2117
Combination of FeII–O Species and Fe–O–Zr Bonds Empowers FeOx Nanoclusters Anchored on UiO-66 Robust H2S-Selective Catalytic Oxidation Performance
The low sulfur selectivity of Fe-based H2S-selective catalytic oxidation catalysts is still a problem, especially at a high O2 content. This is alleviated here through anchoring FeO x nanoclusters on UiO-66 via the formation of Fe-O-Zr bonds. The introduced FeO x species exist in the form of FeIII and FeII. Therein the FeIII-O species are the predominant active sites for H2S-oxidation. The formed Fe-O-Zr bonds strengthen the redox cycle of FeIII/FeII through promoting electron transfer from Fe to Zr. The FeII-O species can activate molecular oxygen to oxidize H2S into elemental S, which accelerates the formation rate of atomic S, hindering its further oxidation into SO2. The combination of these factors empowers the catalysts, enabling 100% H2S conversion and 98.2% sulfur yield. The catalyst also has satisfactory stability with the sulfur selectivity only decreasing from 98.2% to 91.3% after the reaction going on 50 h. The decreased sulfur selectivity might be caused by the deterioration of pores and the deposition of elemental S on the surface. The former hinders the diffusion of sulfur oligomers timely from pores to the gas phase, while the latter is suspected to capture electrons to promote its further reaction with molecular oxygen.
- 18 January 2025
- Published by American Chemical Society (ACS) in Inorganic Chemistry
- Vol. 64 (4) , 2106-2117
Combination of FeII–O Species and Fe–O–Zr Bonds Empowers FeOx Nanoclusters Anchored on UiO-66 Robust H2S-Selective Catalytic Oxidation Performance
The low sulfur selectivity of Fe-based H2S-selective catalytic oxidation catalysts is still a problem, especially at a high O2 content. This is alleviated here through anchoring FeO x nanoclusters on UiO-66 via the formation of Fe-O-Zr bonds. The introduced FeO x species exist in the form of FeIII and FeII. Therein the FeIII-O species are the predominant active sites for H2S-oxidation. The formed Fe-O-Zr bonds strengthen the redox cycle of FeIII/FeII through promoting electron transfer from Fe to Zr. The FeII-O species can activate molecular oxygen to oxidize H2S into elemental S, which accelerates the formation rate of atomic S, hindering its further oxidation into SO2. The combination of these factors empowers the catalysts, enabling 100% H2S conversion and 98.2% sulfur yield. The catalyst also has satisfactory stability with the sulfur selectivity only decreasing from 98.2% to 91.3% after the reaction going on 50 h. The decreased sulfur selectivity might be caused by the deterioration of pores and the deposition of elemental S on the surface. The former hinders the diffusion of sulfur oligomers timely from pores to the gas phase, while the latter is suspected to capture electrons to promote its further reaction with molecular oxygen.
- 21 March 2023
- Published by Elsevier in Journal of Colloid and Interface Science
- Vol. 641, 707-718
Synergistic effect of bimetal in isoreticular Zn–Cu–1,3,5-benzenetricarboxylate on room temperature gaseous sulfides removal
- 21 March 2023
- Published by Elsevier in Journal of Colloid and Interface Science
- Vol. 641, 707-718
Synergistic effect of bimetal in isoreticular Zn–Cu–1,3,5-benzenetricarboxylate on room temperature gaseous sulfides removal
- Open Access
- 15 March 2023
- Published by Elsevier in Resources Chemicals and Materials
- Vol. 2 (2) , 143-150
In-situ preparation of Cu-BTC modified with organic amines for H2S removal under ambient conditions
- 15 March 2023
- Published by Elsevier in Resources Chemicals and Materials
- Vol. 2 (2) , 143-150
Open AccessIn-situ preparation of Cu-BTC modified with organic amines for H2S removal under ambient conditions
- 6 August 2022
- Published by Springer Nature in Journal of Inorganic and Organometallic Polymers and Materials
- Vol. 32 (12) , 4549-4558
Further Use of Spent Co-Based Macroporous Adsorbent for Low-Temperature Hydrodesulfurization
- 6 August 2022
- Published by Springer Nature in Journal of Inorganic and Organometallic Polymers and Materials
- Vol. 32 (12) , 4549-4558
Further Use of Spent Co-Based Macroporous Adsorbent for Low-Temperature Hydrodesulfurization
- Open Access
- 25 March 2022
- Published by Springer Nature in Research Square
Further Use of Spent Co-Based Macroporous Adsorbent for Low-Temperature Hydrodesulfurization
Solid waste Co-containing adsorbents are considered to be used for the hydrotreating process. Herein, Cobalt-based waste materials from the low-temperature desulfurization process were used as organic sulfur hydrotreating catalysts. Physicochemical properties of waste adsorbents were characterized and the performance for COS conversion was evaluated at different conditions. The spent Co-containing adsorbents exhibit considerable organic sulfur hydrogenation performance at low temperature, the residual cobalt oxide in sulfided samples will absorb part of hydrogen sulfide and generate new active phase Co9S8. By further characterization, it can be found that the unstable Co-S bond on the surface of the sample played a key role in hydrogenation catalysis. Results indicated that the sulfidation degree of the waste adsorbents played a key role in the hydrotreating process. With the temperature increasing from 150~250 ℃, the conversion rate and H2S selectivity were increased. It is hoped that this paper will provide significant suggestions in waste adsorbents treatment for future work.
- 25 March 2022
- Published by Springer Nature in Research Square
Open AccessFurther Use of Spent Co-Based Macroporous Adsorbent for Low-Temperature Hydrodesulfurization
Solid waste Co-containing adsorbents are considered to be used for the hydrotreating process. Herein, Cobalt-based waste materials from the low-temperature desulfurization process were used as organic sulfur hydrotreating catalysts. Physicochemical properties of waste adsorbents were characterized and the performance for COS conversion was evaluated at different conditions. The spent Co-containing adsorbents exhibit considerable organic sulfur hydrogenation performance at low temperature, the residual cobalt oxide in sulfided samples will absorb part of hydrogen sulfide and generate new active phase Co9S8. By further characterization, it can be found that the unstable Co-S bond on the surface of the sample played a key role in hydrogenation catalysis. Results indicated that the sulfidation degree of the waste adsorbents played a key role in the hydrotreating process. With the temperature increasing from 150~250 ℃, the conversion rate and H2S selectivity were increased. It is hoped that this paper will provide significant suggestions in waste adsorbents treatment for future work.
- 1 December 2019
- Published by Elsevier in Applied Surface Science
- Vol. 497
Adsorption of hydrogen sulfide by amine-functionalized metal organic framework (MOF-199): An experimental and simulation study
- 1 December 2019
- Published by Elsevier in Applied Surface Science
- Vol. 497
Adsorption of hydrogen sulfide by amine-functionalized metal organic framework (MOF-199): An experimental and simulation study