Shaoyuan Shi
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
Shaoyuan Shi has a total of 41 co-authors. Here are the top co-authors by number of shared publications:
Hongbin Cao
Key Laboratory of Green Process and Engineering, Beijing Engineering Research Center of Process Pollution Control, Innovation Academy for Green Manufacture, Institute of Process Engineering, Chinese Academy of Sciences, Beijing, 100190, China
4 shared publicationsYujiao Li
School of Ecology and Environment, Beijing Technology and Business University, Beijing 100048, China
4 shared publicationsZhijuan Zhao
Key Laboratory of Green Process and Engineering, Beijing Engineering Research Center of Process Pollution Control, Innovation Academy for Green Manufacture, Institute of Process Engineering, Chinese Academy of Sciences, Beijing, 100190, China
4 shared publications- Hongbin Cao
Chemistry & Chemical Engineering Data Center, Institute of Process Engineering, Chinese Academy of Sciences, Beijing 100190, China
3 shared publications Renqiang Cao
National Key Laboratory of Biochemical Engineering, National Engineering Research Center of Green Recycling for Strategic Metal Resources, Beijing Engineering Research Centre of Process Pollution Control, Institute of Process Engineering, Innovation Academy for Green Manufacture, Chinese Academy of Sciences, Beijing 100190, China
3 shared publicationsFeng Duan
Key Laboratory of Green Process and Engineering, Beijing Engineering Research Center of Process Pollution Control, Innovation Academy for Green Manufacture, Institute of Process Engineering, Chinese Academy of Sciences, Beijing, 100190, China
2 shared publications
Latest Publications
- 28 August 2025
- Published by American Chemical Society (ACS) in ACS Applied Polymer Materials
- Vol. 7 (17) , 11227-11236
Effects of Monomer Type on Polyphenol-Amine Codeposition and Its Application in Antifouling Modification of Anion Exchange Membranes (AEMs)
- 28 August 2025
- Published by American Chemical Society (ACS) in ACS Applied Polymer Materials
- Vol. 7 (17) , 11227-11236
Effects of Monomer Type on Polyphenol-Amine Codeposition and Its Application in Antifouling Modification of Anion Exchange Membranes (AEMs)
- 21 September 2023
- Published by American Chemical Society (ACS) in ACS Applied Nano Materials
- Vol. 6 (19) , 18255-18262
GO–Polymer Modified Anion Exchange Membranes for Antifouling
- 21 September 2023
- Published by American Chemical Society (ACS) in ACS Applied Nano Materials
- Vol. 6 (19) , 18255-18262
GO–Polymer Modified Anion Exchange Membranes for Antifouling
- Open Access
Separation of Hydrochloric Acid and Oxalic Acid from Rare Earth Oxalic Acid Precipitation Mother Liquor by Electrodialysis
In this study, the hydrochloric acid from rare earth oxalic acid precipitation mother liquor was separated by electrodialysis (ED) with different anion exchange membranes, including selective anion exchange membrane (SAEM), polymer alloy anion exchange membrane (PAAEM), and homogenous anion exchange membrane (HAEM). In addition to actual wastewater, nine types of simulated solutions with different concentrations of hydrochloric acid and oxalic acid were used in the experiments. The results indicated that the hydrochloric acid could be separated effectively by electrodialysis with SAEM from simulated and real rare earth oxalic acid precipitation mother liquor under the operating voltage 15 V and ampere 2.2 A, in which the hydrochloric acid obtained in the concentrate chamber of ED is of higher purity (>91.5%) generally. It was found that the separation effect of the two acids was related to the concentrations and molar ratios of hydrochloric acid and oxalic acid contained in their mixtures. The SEM images and ESD–mapping analyses indicated that membrane fouling appeared on the surface of ACS and CSE at the diluted side of the ED membrane stack when electrodialysis was used to treat the real rare earth oxalic acid precipitation mother liquor. Fe, Yb, Al, and Dy were found in the CSE membrane section, and organic compounds containing carbon and sulfur were attached to the surface of the ACS. The results also indicated that the real rare earth precipitation mother liquor needed to be pretreated before the separation of hydrochloric acid and oxalic acid by electrodialysis.
Open AccessSeparation of Hydrochloric Acid and Oxalic Acid from Rare Earth Oxalic Acid Precipitation Mother Liquor by Electrodialysis
In this study, the hydrochloric acid from rare earth oxalic acid precipitation mother liquor was separated by electrodialysis (ED) with different anion exchange membranes, including selective anion exchange membrane (SAEM), polymer alloy anion exchange membrane (PAAEM), and homogenous anion exchange membrane (HAEM). In addition to actual wastewater, nine types of simulated solutions with different concentrations of hydrochloric acid and oxalic acid were used in the experiments. The results indicated that the hydrochloric acid could be separated effectively by electrodialysis with SAEM from simulated and real rare earth oxalic acid precipitation mother liquor under the operating voltage 15 V and ampere 2.2 A, in which the hydrochloric acid obtained in the concentrate chamber of ED is of higher purity (>91.5%) generally. It was found that the separation effect of the two acids was related to the concentrations and molar ratios of hydrochloric acid and oxalic acid contained in their mixtures. The SEM images and ESD–mapping analyses indicated that membrane fouling appeared on the surface of ACS and CSE at the diluted side of the ED membrane stack when electrodialysis was used to treat the real rare earth oxalic acid precipitation mother liquor. Fe, Yb, Al, and Dy were found in the CSE membrane section, and organic compounds containing carbon and sulfur were attached to the surface of the ACS. The results also indicated that the real rare earth precipitation mother liquor needed to be pretreated before the separation of hydrochloric acid and oxalic acid by electrodialysis.
- Open Access
- 15 July 2022
- Published by American Chemical Society (ACS) in ACS Omega
- Vol. 7 (29) , 25686-25692
Novel B and N Sites of One-Dimensional Boron Nitride Fiber: Efficient Performance and Mechanism in the Formaldehyde Capture Process
Identification of adsorption centers with atomic levels of adsorbents is crucial to study the adsorption of formaldehyde (HCHO), especially for an in-depth understanding of the mechanism of HCHO capture. Herein, we investigate the HCHO adsorption performance of one-dimensional (1D) nano-porous boron nitride (BN) fiber, and explore the adsorption mechanism by density functional theory (DFT) calculations, including adsorption energy change and Bader charge change, and experimental study as well. Research shows that the 1D nanoporous BN fiber possesses a high concentration of Lewis pairs, which act as Lewis acid and Lewis base sites associated with the fiber's electron-deficient and electron-rich features. It is worth noting that the HCHO removal efficiency of a typical sample is as high as 91%. This work may open the door to the field of adsorption of other pollutants by constructing Lewis pairs in the future.
- 15 July 2022
- Published by American Chemical Society (ACS) in ACS Omega
- Vol. 7 (29) , 25686-25692
Open AccessNovel B and N Sites of One-Dimensional Boron Nitride Fiber: Efficient Performance and Mechanism in the Formaldehyde Capture Process
Identification of adsorption centers with atomic levels of adsorbents is crucial to study the adsorption of formaldehyde (HCHO), especially for an in-depth understanding of the mechanism of HCHO capture. Herein, we investigate the HCHO adsorption performance of one-dimensional (1D) nano-porous boron nitride (BN) fiber, and explore the adsorption mechanism by density functional theory (DFT) calculations, including adsorption energy change and Bader charge change, and experimental study as well. Research shows that the 1D nanoporous BN fiber possesses a high concentration of Lewis pairs, which act as Lewis acid and Lewis base sites associated with the fiber's electron-deficient and electron-rich features. It is worth noting that the HCHO removal efficiency of a typical sample is as high as 91%. This work may open the door to the field of adsorption of other pollutants by constructing Lewis pairs in the future.
- 12 October 2021
- Published by American Chemical Society (ACS) in Environmental Science & Technology
- Vol. 55 (21) , 14886-14896
Bipolar Membrane Electrodialysis for Ammonia Recovery from Synthetic Urine: Experiments, Modeling, and Performance Analysis
Recovering nitrogen from source-separated urine is an important part of the sustainable nitrogen management. A novel bipolar membrane electrodialysis with membrane contactor (BMED–MC) process is demonstrated here for efficient recovery of ammonia from synthetic source-separated urine (∼3772 mg N L–1). In a BMED–MC process, electrically driven water dissociation in a bipolar membrane simultaneously increases the pH of the urine stream and produces an acid stream for ammonia stripping. With the increased pH of urine, ammonia transports across the gas-permeable membrane in the membrane contactor and is recovered by the acid stream as ammonium sulfate that can be directly used as fertilizer. Our results obtained using batch experiments demonstrate that the BMED–MC process can achieve 90% recovery. The average ammonia flux and the specific energy consumption can be regulated by varying the current density. At a current density of 20 mA cm–2, the energy required to achieve a 67.5% ammonia recovery in a 7 h batch mode is 92.8 MJ kg–1 N for a bench-scale system with one membrane stack and can approach 25.8 MJ kg–1 N for large-scale systems with multiple membrane stacks, with an average ammonia flux of 2.2 mol m–2 h–1. Modeling results show that a continuous BMED–MC process can achieve a 90% ammonia recovery with a lower energy consumption (i.e., 12.5 MJ kg–1 N). BMED–MC shows significant potential for ammonia recovery from source-separated urine as it is relatively energy-efficient and requires no external acid solution.
- 12 October 2021
- Published by American Chemical Society (ACS) in Environmental Science & Technology
- Vol. 55 (21) , 14886-14896
Bipolar Membrane Electrodialysis for Ammonia Recovery from Synthetic Urine: Experiments, Modeling, and Performance Analysis
Recovering nitrogen from source-separated urine is an important part of the sustainable nitrogen management. A novel bipolar membrane electrodialysis with membrane contactor (BMED–MC) process is demonstrated here for efficient recovery of ammonia from synthetic source-separated urine (∼3772 mg N L–1). In a BMED–MC process, electrically driven water dissociation in a bipolar membrane simultaneously increases the pH of the urine stream and produces an acid stream for ammonia stripping. With the increased pH of urine, ammonia transports across the gas-permeable membrane in the membrane contactor and is recovered by the acid stream as ammonium sulfate that can be directly used as fertilizer. Our results obtained using batch experiments demonstrate that the BMED–MC process can achieve 90% recovery. The average ammonia flux and the specific energy consumption can be regulated by varying the current density. At a current density of 20 mA cm–2, the energy required to achieve a 67.5% ammonia recovery in a 7 h batch mode is 92.8 MJ kg–1 N for a bench-scale system with one membrane stack and can approach 25.8 MJ kg–1 N for large-scale systems with multiple membrane stacks, with an average ammonia flux of 2.2 mol m–2 h–1. Modeling results show that a continuous BMED–MC process can achieve a 90% ammonia recovery with a lower energy consumption (i.e., 12.5 MJ kg–1 N). BMED–MC shows significant potential for ammonia recovery from source-separated urine as it is relatively energy-efficient and requires no external acid solution.
- 2 January 2020
- Published by American Chemical Society (ACS) in ACS Applied Nano Materials
- Vol. 3 (1) , 588-596
Anion Exchange Nanocomposite Membranes Modified with Graphene Oxide and Polydopamine: Interfacial Structure and Antifouling Applications
- 2 January 2020
- Published by American Chemical Society (ACS) in ACS Applied Nano Materials
- Vol. 3 (1) , 588-596
Anion Exchange Nanocomposite Membranes Modified with Graphene Oxide and Polydopamine: Interfacial Structure and Antifouling Applications
- 1 March 2019
- Published by Elsevier in Journal of Environmental Sciences
- Vol. 77, 218-228
Comparative studies on fouling of homogeneous anion exchange membranes by different structured organics in electrodialysis
- 1 March 2019
- Published by Elsevier in Journal of Environmental Sciences
- Vol. 77, 218-228
Comparative studies on fouling of homogeneous anion exchange membranes by different structured organics in electrodialysis
- 29 May 2018
- Published by Pleiades Publishing Ltd in Russian Journal of Physical Chemistry A
- Vol. 92 (6) , 1229-1236
Comparative Study of Chromium(VI) Removal from Simulated Industrial Wastewater with Ion Exchange Resins
Ion exchange process is an alternative technique for removal of heavy metal ions from industrial wastewater. The main aim of this paper is to evaluate the performance of different ion exchange resins...
- 29 May 2018
- Published by Pleiades Publishing Ltd in Russian Journal of Physical Chemistry A
- Vol. 92 (6) , 1229-1236
Comparative Study of Chromium(VI) Removal from Simulated Industrial Wastewater with Ion Exchange Resins
Ion exchange process is an alternative technique for removal of heavy metal ions from industrial wastewater. The main aim of this paper is to evaluate the performance of different ion exchange resins...
- 1 February 2016
- Published by Elsevier in Water Research
- Vol. 89, 201-209
Bipolar membrane electrodialysis for generation of hydrochloric acid and ammonia from simulated ammonium chloride wastewater
- 1 February 2016
- Published by Elsevier in Water Research
- Vol. 89, 201-209
Bipolar membrane electrodialysis for generation of hydrochloric acid and ammonia from simulated ammonium chloride wastewater