Gang Yang
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Gang Yang has a total of 22 co-authors. Here are the top co-authors by number of shared publications:
Dong-Ling Qin
State Key Laboratory of Materials-Oriented Chemical Engineering, College of Chemical Engineering, Nanjing Tech University, Nanjing 210009, China
1 shared publicationDongling Qin
Nanjing Tech University
1 shared publication- Haijun Zhang
College of Chemical Engineering, Nanjing Tech University, State Key Laboratory of Materials-Oriented Chemical Engineering, Nanjing, China
1 shared publication Le Han
State Key Laboratory of Materials-Oriented Chemical Engineering, College of Chemical Engineering, Nanjing Tech University, Nanjing 210009, China
1 shared publicationLei Chen
State Key Laboratory of Materials-Oriented Chemical Engineering, College of Chemical Engineering, Nanjing Tech University, Nanjing, China
1 shared publicationShiyu Yan
State Key Laboratory of Materials-Oriented Chemical Engineering, College of Chemical Engineering, Nanjing Tech University, Nanjing, China
1 shared publication
Latest Publications
- 29 June 2026
- Published by Springer Nature in JOM
- Vol. 78 (10) , 1-11
Synergistic Utilization of Aluminum Anodizing Sludge and Foil Industry Waste Acid: A Study on Leaching Kinetics and Resource Recovery
- 29 June 2026
- Published by Springer Nature in JOM
- Vol. 78 (10) , 1-11
Synergistic Utilization of Aluminum Anodizing Sludge and Foil Industry Waste Acid: A Study on Leaching Kinetics and Resource Recovery
- 1 August 2025
- Published by Springer Nature in Research on Chemical Intermediates
- Vol. 51 (9) , 4811-4827
Myristyl sulfobetaine-assisted synthesis of SAPO-34 molecular sieves with improved methanol-to-olefins (MTO) performance
- 1 August 2025
- Published by Springer Nature in Research on Chemical Intermediates
- Vol. 51 (9) , 4811-4827
Myristyl sulfobetaine-assisted synthesis of SAPO-34 molecular sieves with improved methanol-to-olefins (MTO) performance
- 23 April 2025
- Published by Springer Nature in Catalysis Letters
- Vol. 155 (5) , 1-14
One-Pot Hydrothermal Synthesis of a Dual-Metal-Modified CuMn-ZSM-5/SAPO-34 Zeolite with Excellent MTO Catalytic Performance
- 23 April 2025
- Published by Springer Nature in Catalysis Letters
- Vol. 155 (5) , 1-14
One-Pot Hydrothermal Synthesis of a Dual-Metal-Modified CuMn-ZSM-5/SAPO-34 Zeolite with Excellent MTO Catalytic Performance
- 17 August 2023
- Published by Springer Nature in Environmental Science and Pollution Research
- Vol. 30 (43) , 97298-97309
Chitosan-stabilized iron-copper nanoparticles for efficient removal of nitrate
Chitosan-stabilized iron-copper nanomaterials (CS-nZVI/Cu) were successfully prepared and applied to the nitrate removal. Batch experiments were conducted to examine the effects of experimental parameters on nitrate removal, including Cu loading, CS-nZVI/Cu dosages, initial nitrate concentrations, and initial pHs. From the experimental date, it was concluded that CS-nZVI/Cu has a high nitrate removal efficiency, which can be more than 97%, respectively, at Cu loading = 5%, dosages of CS-nZVI/Cu = 3 g/L, initial nitrate concentrations of 30~120 mg/L, and initial pH values = 2~9. Additionally, the kinetic data for CS-nZVI/Cu were found to fit well with the first-order kinetic model with a rate constant of 0.15 (mg∙L)1-n/min, where n=1. The Langmuir model showed a good fit for NO3- removal, indicating that monolayer chemisorption occurred. The SEM and TEM analyses showed that the addition of chitosan resulted in improved dispersion of the CS-nZVI/Cu. The CS-nZVI/Cu nanomaterials have a more complete elliptical shape and are between 50 and 100 nm in size. The XRD analysis showed that the chitosan encapsulation reduced the oxidation of the iron component and the main product was Fe3O4. The FT-IR analysis showed that the immobilization of chitosan and the iron was accomplished by the ligand interaction. The nitrogen adsorption-desorption isotherm results showed that the CS-nZVI/Cu specific surface area and pore volume decreased significantly after the reaction. Adsorption, oxidation, and reduction are possible mechanisms for nitrate removal by CS-nZVI/Cu. The XPS analysis investigated the contribution of nZVI and Cu in the removal mechanism. Adding copper accelerates the reaction time and rate. In addition, nZVI played a vital role in reducing nitrate to N2. Based on these results, it looks like CS-nZVI/Cu could be a satisfactory material for nitrate removal.
- 17 August 2023
- Published by Springer Nature in Environmental Science and Pollution Research
- Vol. 30 (43) , 97298-97309
Chitosan-stabilized iron-copper nanoparticles for efficient removal of nitrate
Chitosan-stabilized iron-copper nanomaterials (CS-nZVI/Cu) were successfully prepared and applied to the nitrate removal. Batch experiments were conducted to examine the effects of experimental parameters on nitrate removal, including Cu loading, CS-nZVI/Cu dosages, initial nitrate concentrations, and initial pHs. From the experimental date, it was concluded that CS-nZVI/Cu has a high nitrate removal efficiency, which can be more than 97%, respectively, at Cu loading = 5%, dosages of CS-nZVI/Cu = 3 g/L, initial nitrate concentrations of 30~120 mg/L, and initial pH values = 2~9. Additionally, the kinetic data for CS-nZVI/Cu were found to fit well with the first-order kinetic model with a rate constant of 0.15 (mg∙L)1-n/min, where n=1. The Langmuir model showed a good fit for NO3- removal, indicating that monolayer chemisorption occurred. The SEM and TEM analyses showed that the addition of chitosan resulted in improved dispersion of the CS-nZVI/Cu. The CS-nZVI/Cu nanomaterials have a more complete elliptical shape and are between 50 and 100 nm in size. The XRD analysis showed that the chitosan encapsulation reduced the oxidation of the iron component and the main product was Fe3O4. The FT-IR analysis showed that the immobilization of chitosan and the iron was accomplished by the ligand interaction. The nitrogen adsorption-desorption isotherm results showed that the CS-nZVI/Cu specific surface area and pore volume decreased significantly after the reaction. Adsorption, oxidation, and reduction are possible mechanisms for nitrate removal by CS-nZVI/Cu. The XPS analysis investigated the contribution of nZVI and Cu in the removal mechanism. Adding copper accelerates the reaction time and rate. In addition, nZVI played a vital role in reducing nitrate to N2. Based on these results, it looks like CS-nZVI/Cu could be a satisfactory material for nitrate removal.
- 17 June 2019
- Published by Springer Nature in Reaction Kinetics, Mechanisms and Catalysis
- Vol. 128 (1) , 523-538
Sulfonic acid-functionalized hierarchical SAPO-34 for fructose dehydration to 5-hydroxymethylfurfural
- 17 June 2019
- Published by Springer Nature in Reaction Kinetics, Mechanisms and Catalysis
- Vol. 128 (1) , 523-538
Sulfonic acid-functionalized hierarchical SAPO-34 for fructose dehydration to 5-hydroxymethylfurfural
- 15 June 2019
- Published by IWA Publishing in Water Science & Technology
- Vol. 79 (12) , 2279-2288
Study on the treatment of simulated azo dye wastewater by a novel micro-electrolysis filler
A new type of iron-copper-carbon (Fe-Cu-C) ternary micro-electrolysis filler was prepared with a certain proportion of iron powder, activated carbon, bentonite, copper powder, etc. The effect of the new type of micro-electrolysis filler on the simulated methyl orange dye wastewater was studied. The effects of various operational parameters, such as reaction time, initial pH value, aeration rate, filler dose and reaction temperature, on the degradation rate of methyl orange were studied to determine the optimum treatment conditions, and the micro-electrolysis filler was characterized by SEM and XRD. The experimental results show that the degradation rate of 220 mL of simulated dye wastewater with a concentration of 100 mg/L reached 93.41% ± 2.94% after 60 mL/min of aeration, with an initial pH = 2, a dose 45 g and 125 minutes of reaction at room temperature. The new micro-electrolysis filler has a high degradation rate for methyl orange solution, which is attributed to the iron and activated carbon particles sintered into an integrated structure, which makes the iron and carbon difficult to separate and affects the galvanic cell reaction. The addition of copper also greatly increases the transmission efficiency of electrons, which promotes the reaction. In addition, the surface iron is consumed, the adjacent carbon is stripped layer by layer, and the new micro-electrolytic filler does not easily passivate and agglomerate during its use.
- 15 June 2019
- Published by IWA Publishing in Water Science & Technology
- Vol. 79 (12) , 2279-2288
Study on the treatment of simulated azo dye wastewater by a novel micro-electrolysis filler
A new type of iron-copper-carbon (Fe-Cu-C) ternary micro-electrolysis filler was prepared with a certain proportion of iron powder, activated carbon, bentonite, copper powder, etc. The effect of the new type of micro-electrolysis filler on the simulated methyl orange dye wastewater was studied. The effects of various operational parameters, such as reaction time, initial pH value, aeration rate, filler dose and reaction temperature, on the degradation rate of methyl orange were studied to determine the optimum treatment conditions, and the micro-electrolysis filler was characterized by SEM and XRD. The experimental results show that the degradation rate of 220 mL of simulated dye wastewater with a concentration of 100 mg/L reached 93.41% ± 2.94% after 60 mL/min of aeration, with an initial pH = 2, a dose 45 g and 125 minutes of reaction at room temperature. The new micro-electrolysis filler has a high degradation rate for methyl orange solution, which is attributed to the iron and activated carbon particles sintered into an integrated structure, which makes the iron and carbon difficult to separate and affects the galvanic cell reaction. The addition of copper also greatly increases the transmission efficiency of electrons, which promotes the reaction. In addition, the surface iron is consumed, the adjacent carbon is stripped layer by layer, and the new micro-electrolytic filler does not easily passivate and agglomerate during its use.