Gang Xue
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Gang Xue has a total of 64 co-authors. Here are the top co-authors by number of shared publications:
- Cairong Gong
Institute of New Energy, School of Materials Science and Engineering, Tianjin University, Tianjin 300072, China
7 shared publications Cairong Gong
School of Materials Science and Engineering, Tianjin University, Tianjin, China
4 shared publications- Jinsheng Liang
Key Laboratory of Special Functional Materials for Ecological Environment and Information (Hebei University of Technology), Ministry of Education, Tianjin, 300130, China; Institute of Power Source and Ecomaterials Science, Hebei University of Technology, Tianjin, 300130, China
3 shared publications Luning Zheng
School of material science and Engineering, Hebei University of Technology, Tianjin, 300401, CHINA
3 shared publicationsXinhui Duan
Key Laboratory of Special Functional Materials for Ecological Environment and Information, Ministry of Education, Hebei University of Technology, Tianjin, China
3 shared publicationsGuangyan Tian
Key Laboratory of Special Functional Materials for Ecological Environment and information, Hebei University of Technology, Ministry of Education, Tianjin 300130, China
2 shared publications
Latest Publications
- 16 September 2026
- Published by Springer Nature in Catalysis Letters
- Vol. 156 (10) , 283
Flash Joule Heating–Driven Fabrication of Defect-Rich Catalysts Derived from Spent Li1.27Mn1.73O4 Batteries for Low-Temperature VOCs Oxidation
- 16 September 2026
- Published by Springer Nature in Catalysis Letters
- Vol. 156 (10) , 283
Flash Joule Heating–Driven Fabrication of Defect-Rich Catalysts Derived from Spent Li1.27Mn1.73O4 Batteries for Low-Temperature VOCs Oxidation
- 24 November 2025
- Published by Springer Nature in Chemical Research in Chinese Universities
- Vol. 41 (6) , 1628-1636
Ultrafast Synthesis of Oxygen Vacancy Rich Pt-Doped La0.6Sr0.4CoO3 with Enhanced Oxygen Evolution Activities
- 24 November 2025
- Published by Springer Nature in Chemical Research in Chinese Universities
- Vol. 41 (6) , 1628-1636
Ultrafast Synthesis of Oxygen Vacancy Rich Pt-Doped La0.6Sr0.4CoO3 with Enhanced Oxygen Evolution Activities
- 4 April 2025
- Published by Springer Nature in Water, Air, & Soil Pollution
- Vol. 236 (5) , 1-20
Performance and Mechanism of Tailings Biochar Composites for Synergistic Phytoremediation of Soil Heavy Metal Cd
- 4 April 2025
- Published by Springer Nature in Water, Air, & Soil Pollution
- Vol. 236 (5) , 1-20
Performance and Mechanism of Tailings Biochar Composites for Synergistic Phytoremediation of Soil Heavy Metal Cd
- 27 March 2025
- Published by Royal Society of Chemistry (RSC) in Journal of Materials Chemistry A
- Vol. 13 (18) , 13469-13481
Performance-enhanced catalysts derived from spent ternary lithium-ion batteries for simultaneous removal of NO x and VOCs
Herein, a performance-enhanced MnCoNiO x catalyst was regenerated from spent lithium ion batteries for simultaneous removal of NO x and benzene, and the effect of lithium ion removal on catalytic materials, especially oxygen vacancies was revealed.
- 27 March 2025
- Published by Royal Society of Chemistry (RSC) in Journal of Materials Chemistry A
- Vol. 13 (18) , 13469-13481
Performance-enhanced catalysts derived from spent ternary lithium-ion batteries for simultaneous removal of NO x and VOCs
Herein, a performance-enhanced MnCoNiO x catalyst was regenerated from spent lithium ion batteries for simultaneous removal of NO x and benzene, and the effect of lithium ion removal on catalytic materials, especially oxygen vacancies was revealed.
- Open Access
Effect of Tourmaline Addition on the Anti-Poisoning Performance of MnCeOx@TiO2 Catalyst for Low-Temperature Selective Catalytic Reduction of NOx
In view of the flue gas characteristics of cement kilns in China, the development of low-temperature denitrification catalysts with excellent anti-poisoning performance has important theoretical and practical significance. In this work, a series of MnCeOx@TiO2 and tourmaline-containing MnCeOx@TiO2-T catalysts was prepared using a chemical pre-deposition method. It was found that the MnCeOx@TiO2-T2 catalyst (containing 2% tourmaline) exhibited the best low-temperature NH3-selective catalytic reduction (NH3-SCR) performance, yielding 100% NOx conversion at 110 °C and above. When 100–300 ppm SO2 and 10 vol.% H2O were introduced to the reaction, the NOx conversion of the MnCeOx@TiO2-T2 catalyst was still higher than 90% at 170 °C, indicating good anti-poisoning performance. The addition of appropriate amounts of tourmaline can not only preferably expose the active {001} facets of TiO2 but also introduce the acidic SiO2 and Al2O3 components and increase the content of Mn4+ and Oα on the surface of the catalyst, all of which contribute to the enhancement of reaction activity of NH3-SCR and anti-poisoning performance. However, excess amounts of tourmaline led to the formation of dense surface of catalysts that suppressed the exposure of catalytic active sites, giving rise to the decrease in catalytic activity and anti-poisoning capability. Through an in situ DRIFTS study, it was found that the addition of appropriate amounts of tourmaline increased the number of Brønsted acid sites on the catalyst surface, which suppressed the adsorption of SO2 and thus inhibited the deposition of NH4HSO4 and (NH4)2HSO4 on the surface of the catalyst, thereby improving the NH3-SCR performance and anti-poisoning ability of the catalyst.
Open AccessEffect of Tourmaline Addition on the Anti-Poisoning Performance of MnCeOx@TiO2 Catalyst for Low-Temperature Selective Catalytic Reduction of NOx
In view of the flue gas characteristics of cement kilns in China, the development of low-temperature denitrification catalysts with excellent anti-poisoning performance has important theoretical and practical significance. In this work, a series of MnCeOx@TiO2 and tourmaline-containing MnCeOx@TiO2-T catalysts was prepared using a chemical pre-deposition method. It was found that the MnCeOx@TiO2-T2 catalyst (containing 2% tourmaline) exhibited the best low-temperature NH3-selective catalytic reduction (NH3-SCR) performance, yielding 100% NOx conversion at 110 °C and above. When 100–300 ppm SO2 and 10 vol.% H2O were introduced to the reaction, the NOx conversion of the MnCeOx@TiO2-T2 catalyst was still higher than 90% at 170 °C, indicating good anti-poisoning performance. The addition of appropriate amounts of tourmaline can not only preferably expose the active {001} facets of TiO2 but also introduce the acidic SiO2 and Al2O3 components and increase the content of Mn4+ and Oα on the surface of the catalyst, all of which contribute to the enhancement of reaction activity of NH3-SCR and anti-poisoning performance. However, excess amounts of tourmaline led to the formation of dense surface of catalysts that suppressed the exposure of catalytic active sites, giving rise to the decrease in catalytic activity and anti-poisoning capability. Through an in situ DRIFTS study, it was found that the addition of appropriate amounts of tourmaline increased the number of Brønsted acid sites on the catalyst surface, which suppressed the adsorption of SO2 and thus inhibited the deposition of NH4HSO4 and (NH4)2HSO4 on the surface of the catalyst, thereby improving the NH3-SCR performance and anti-poisoning ability of the catalyst.
- 1 February 2024
- Published by Springer Nature in Catalysis Letters
- Vol. 154 (7) , 3516-3529
Synergistic Removal of NOx and VOCs from Flue Gas on Mn-Based Catalysts
- 1 February 2024
- Published by Springer Nature in Catalysis Letters
- Vol. 154 (7) , 3516-3529
Synergistic Removal of NOx and VOCs from Flue Gas on Mn-Based Catalysts
- 21 January 2024
- Published by Elsevier in Journal of Materials Science & Technology
- Vol. 191, 1-7
Ultrafast nanomanufacturing via high-temperature shock of La0.6Sr0.4CoO3 catalysts for overall water splitting
- 21 January 2024
- Published by Elsevier in Journal of Materials Science & Technology
- Vol. 191, 1-7
Ultrafast nanomanufacturing via high-temperature shock of La0.6Sr0.4CoO3 catalysts for overall water splitting
- Open Access
- 5 October 2023
- Published by IWA Publishing in Water Science & Technology
- Vol. 88 (8) , 1927-1943
Degradation of bisphenol A by persulfate activation of MoS2 composite iron tailings
In this paper, molybdenum disulfide was grown on the surface of iron-containing tailings by hydrothermal method, and a series of highly efficient activated persulfate (PMS) iron-based catalysts were successfully prepared. The results show that in the CTM 1–200/PMS system, the additional ratio of tailings and the hydrothermal temperature have important effects on the catalyst. The catalyst prepared under the conditions of CT:MoS2 (molar ratio 1:1) and hydrothermal temperature of 200 °C (CTM 1–200) had the best degradation effect on BPA, and the degradation effect was increased by four times. The reason for the improvement of degradation efficiency is that the introduction of MoS2 accelerates the REDOX cycle between Fe(II)/Fe(III), and the reduction of Fe(III) is mainly related to Mo(IV), while the reduction capacity of S is relatively weak. Molybdenum disulfide/iron tailing composite material provides a way for tailings to solve the problem of water pollution.
- 5 October 2023
- Published by IWA Publishing in Water Science & Technology
- Vol. 88 (8) , 1927-1943
Open AccessDegradation of bisphenol A by persulfate activation of MoS2 composite iron tailings
In this paper, molybdenum disulfide was grown on the surface of iron-containing tailings by hydrothermal method, and a series of highly efficient activated persulfate (PMS) iron-based catalysts were successfully prepared. The results show that in the CTM 1–200/PMS system, the additional ratio of tailings and the hydrothermal temperature have important effects on the catalyst. The catalyst prepared under the conditions of CT:MoS2 (molar ratio 1:1) and hydrothermal temperature of 200 °C (CTM 1–200) had the best degradation effect on BPA, and the degradation effect was increased by four times. The reason for the improvement of degradation efficiency is that the introduction of MoS2 accelerates the REDOX cycle between Fe(II)/Fe(III), and the reduction of Fe(III) is mainly related to Mo(IV), while the reduction capacity of S is relatively weak. Molybdenum disulfide/iron tailing composite material provides a way for tailings to solve the problem of water pollution.
- 8 February 2023
- Published by American Chemical Society (ACS) in ACS Applied Energy Materials
- Vol. 6 (4) , 2207-2218
Lamellar Carbon Composited Cobalt Iron Silicate with a Two-Dimensional Structure Toward Enhanced Electrochemical Properties for Supercapacitors
- 8 February 2023
- Published by American Chemical Society (ACS) in ACS Applied Energy Materials
- Vol. 6 (4) , 2207-2218
Lamellar Carbon Composited Cobalt Iron Silicate with a Two-Dimensional Structure Toward Enhanced Electrochemical Properties for Supercapacitors
- Open Access
- 31 March 2022
- Published by IWA Publishing in Water Science & Technology
- Vol. 85 (8) , 2332-2349
Recycling iron from pickling sludge to activate peroxydisulfate for the degradation of phenol
In this work, iron was recovered from a kind of iron-rich pickling sludge by an acid leaching process, and the recycled iron was used as a catalyst to activate peroxydisulfate (PS) for the degradation of phenol. Different kinds of sludge catalysts were prepared by different drying methods such as ordinary drying (Ods), freeze drying (Fds) and vacuum drying (Vds). The degradation performance of the different catalysts/PS system under different conditions was explored, the vacuum drying sludge catalyst (Vds) has the best activity in a wide pH range (pH = 3–10) and a wide temperature range (0–40 °C). At the same time, the effect of a series of chelating agents (Oxalic acid (OA), Citric acid (CA), Tartaric acid (TA), Malic acid (DL-MA) and Ethylenediaminetetraacetic acid (EDTA)) on Vds/PS system was verified, and TA was selected as the best chelating agent to promote the degradation of the second stage where the degradation rate is limited. The quenching experiment and electron paramagnetic resonance (EPR) analysis indicated that hydroxyl radical (·OH) and sulfate radical (SO4̇−) were responsible for the abatement of the organic contaminant with ·OH playing a more important role. In summary, this study proposed an environmentally-friendly approach for the application of iron-rich pickling sludge in the remediation of phenol-contaminated water.
- 31 March 2022
- Published by IWA Publishing in Water Science & Technology
- Vol. 85 (8) , 2332-2349
Open AccessRecycling iron from pickling sludge to activate peroxydisulfate for the degradation of phenol
In this work, iron was recovered from a kind of iron-rich pickling sludge by an acid leaching process, and the recycled iron was used as a catalyst to activate peroxydisulfate (PS) for the degradation of phenol. Different kinds of sludge catalysts were prepared by different drying methods such as ordinary drying (Ods), freeze drying (Fds) and vacuum drying (Vds). The degradation performance of the different catalysts/PS system under different conditions was explored, the vacuum drying sludge catalyst (Vds) has the best activity in a wide pH range (pH = 3–10) and a wide temperature range (0–40 °C). At the same time, the effect of a series of chelating agents (Oxalic acid (OA), Citric acid (CA), Tartaric acid (TA), Malic acid (DL-MA) and Ethylenediaminetetraacetic acid (EDTA)) on Vds/PS system was verified, and TA was selected as the best chelating agent to promote the degradation of the second stage where the degradation rate is limited. The quenching experiment and electron paramagnetic resonance (EPR) analysis indicated that hydroxyl radical (·OH) and sulfate radical (SO4̇−) were responsible for the abatement of the organic contaminant with ·OH playing a more important role. In summary, this study proposed an environmentally-friendly approach for the application of iron-rich pickling sludge in the remediation of phenol-contaminated water.