Zhujian Huang
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Zhujian Huang has a total of 130 co-authors. Here are the top co-authors by number of shared publications:
- Pingxiao Wu
South China University of Technology
13 shared publications Lihua Cui
11 shared publicationsNengwu Zhu
College of Environmental and Energy, South China University of Technology, Guangzhou 510006, PR China; The Key Laboratory of Pollution Control and Ecosystem Restoration in Industry Clusters, Ministry of Education, Guangzhou 510006, PR China; The Key Laboratory of Environmental Protection and Eco-Remediation of Guangdong Regular Higher Education Institutions, PR China
9 shared publicationsBeini Gong
7 shared publicationsJunhong Liu
Guangdong Laboratory for Lingnan Modern Agriculture, College of Natural Resources and Environment, South China Agricultural University, 483 Wushan St, Guangzhou 510642, China; Guangdong Provincial Key Laboratory of Agricultural & Rural Pollution Abatement and Environmental Safety, College of Natural Resources and Environment, South China Agricultural University, 483 Wushan St., Guangzhou 510642, China
6 shared publicationsXuewen Luo
Guangdong Provincial Key Laboratory of Agricultural & Rural Pollution Abatement and Environmental Safety, College of Natural Resources and Environment, South China Agricultural University, 483 Wushan Street, Guangzhou 510642, China
6 shared publications
Latest Publications
- 22 October 2025
- Published by American Chemical Society (ACS) in ACS ES&T Water
- Vol. 5 (11) , 7028-7038
Efficient Cr(VI) Removal Using Layered Double Hydroxides as Anode Materials in Asymmetric Flow-Electrode Capacitive Deionization
- 22 October 2025
- Published by American Chemical Society (ACS) in ACS ES&T Water
- Vol. 5 (11) , 7028-7038
Efficient Cr(VI) Removal Using Layered Double Hydroxides as Anode Materials in Asymmetric Flow-Electrode Capacitive Deionization
- 10 February 2025
- Published by Elsevier in Journal of Environmental Management
- Vol. 376, 124423
Electrochemically driven inactivation of harmful cyanobacteria assisted with the visible light photocatalyst of CeO2-Fe3O4-CQDs
- 10 February 2025
- Published by Elsevier in Journal of Environmental Management
- Vol. 376, 124423
Electrochemically driven inactivation of harmful cyanobacteria assisted with the visible light photocatalyst of CeO2-Fe3O4-CQDs
- 5 February 2025
- Published by Springer Nature in Environmental Science and Pollution Research
- Vol. 32 (9) , 5132-5142
Green synthesis of zeolite and its regeneration for adsorption of ammonia nitrogen in water
This study presents a novel green approach for the preparation of zeolite material from fly ash using a combination of mechanochemical methods. The physicochemical properties of the synthesized zeolite, including crystal structure and porosity, were systematically investigated. The synthesized zeolite was employed for the adsorption of ammonia nitrogen from aqueous solutions, and their adsorption kinetics and thermodynamics were comprehensively studied. The results revealed that the adsorption of ammonia nitrogen onto the zeolite follows the Langmuir adsorption model. Additionally, the zeolite exhibited strong selective adsorption and remarkable resistance to interference from coexisting cations in the aqueous solution. Finally, regeneration experiments were conducted using NaCl, NaClO, and their mixtures to desorb ammonia nitrogen from the spent zeolite. A total of 17 regeneration cycles were performed until the adsorption capacity of the zeolites was exhausted. The adsorption performance of the regenerated zeolite was evaluated to assess the impact of different reagents and regeneration cycles on adsorption efficiency. The optimal regeneration method was identified, leading to the successful valorization of fly ash into zeolite for ammonia adsorption and the development of effective regeneration strategies for spent zeolite.
- 5 February 2025
- Published by Springer Nature in Environmental Science and Pollution Research
- Vol. 32 (9) , 5132-5142
Green synthesis of zeolite and its regeneration for adsorption of ammonia nitrogen in water
This study presents a novel green approach for the preparation of zeolite material from fly ash using a combination of mechanochemical methods. The physicochemical properties of the synthesized zeolite, including crystal structure and porosity, were systematically investigated. The synthesized zeolite was employed for the adsorption of ammonia nitrogen from aqueous solutions, and their adsorption kinetics and thermodynamics were comprehensively studied. The results revealed that the adsorption of ammonia nitrogen onto the zeolite follows the Langmuir adsorption model. Additionally, the zeolite exhibited strong selective adsorption and remarkable resistance to interference from coexisting cations in the aqueous solution. Finally, regeneration experiments were conducted using NaCl, NaClO, and their mixtures to desorb ammonia nitrogen from the spent zeolite. A total of 17 regeneration cycles were performed until the adsorption capacity of the zeolites was exhausted. The adsorption performance of the regenerated zeolite was evaluated to assess the impact of different reagents and regeneration cycles on adsorption efficiency. The optimal regeneration method was identified, leading to the successful valorization of fly ash into zeolite for ammonia adsorption and the development of effective regeneration strategies for spent zeolite.
- 8 November 2024
- Published by American Chemical Society (ACS) in ACS ES&T Water
- Vol. 4 (12) , 5821-5833
Synergy of Free Radicals in Microcystis aeruginosa Inactivation within an Electrolysis/Persulfate/Chlorine System
- 8 November 2024
- Published by American Chemical Society (ACS) in ACS ES&T Water
- Vol. 4 (12) , 5821-5833
Synergy of Free Radicals in Microcystis aeruginosa Inactivation within an Electrolysis/Persulfate/Chlorine System
- Open Access
Activation of Persulfate by NiFe-Layered Double Hydroxides Toward Efficient Degradation of Doxycycline in Water
In recent years, the excessive use and improper disposal of antibiotics have led to their pervasive presence in the environment, resulting in significant antibiotic pollution. To address this pressing issue, the present study synthesized nickel–iron-layered double hydroxides (NiFe-LDHs) with varying molar ratios using a hydrothermal method, employing these LDHs as catalysts for the oxidative degradation of doxycycline, with peroxymonosulfate (PMS) serving as the oxidant. X-ray diffraction analysis confirmed that the synthesized NiFe-LDHs exhibited a hexagonal crystal structure characteristic of layered double hydroxides. Experimental results demonstrated that the catalytic efficiency of NiFe-LDHs increased with both the dosage of the catalyst and the concentration of PMS, achieving a high degradation efficiency for doxycycline at a catalyst concentration of 0.5 g/L. Furthermore, the catalytic performance was notably effective across a range of pH conditions, with the highest degradation efficiency being observed at a Ni–Fe molar ratio of 3:1. The activation of PMS by NiFe-LDHs for the catalytic degradation of pollutants primarily occurs through singlet oxygen (1O2), superoxide radicals (O2−·), and sulfate radicals (SO4−·). The study also proposed three potential degradation pathways for doxycycline, indicating that the final degradation products have lower environmental toxicity. This research offers novel approaches and methodologies for the treatment of antibiotic-contaminated wastewater.
Open AccessActivation of Persulfate by NiFe-Layered Double Hydroxides Toward Efficient Degradation of Doxycycline in Water
In recent years, the excessive use and improper disposal of antibiotics have led to their pervasive presence in the environment, resulting in significant antibiotic pollution. To address this pressing issue, the present study synthesized nickel–iron-layered double hydroxides (NiFe-LDHs) with varying molar ratios using a hydrothermal method, employing these LDHs as catalysts for the oxidative degradation of doxycycline, with peroxymonosulfate (PMS) serving as the oxidant. X-ray diffraction analysis confirmed that the synthesized NiFe-LDHs exhibited a hexagonal crystal structure characteristic of layered double hydroxides. Experimental results demonstrated that the catalytic efficiency of NiFe-LDHs increased with both the dosage of the catalyst and the concentration of PMS, achieving a high degradation efficiency for doxycycline at a catalyst concentration of 0.5 g/L. Furthermore, the catalytic performance was notably effective across a range of pH conditions, with the highest degradation efficiency being observed at a Ni–Fe molar ratio of 3:1. The activation of PMS by NiFe-LDHs for the catalytic degradation of pollutants primarily occurs through singlet oxygen (1O2), superoxide radicals (O2−·), and sulfate radicals (SO4−·). The study also proposed three potential degradation pathways for doxycycline, indicating that the final degradation products have lower environmental toxicity. This research offers novel approaches and methodologies for the treatment of antibiotic-contaminated wastewater.
- Open Access
- 4 October 2024
- Published by Springer Nature in Research Square
Green synthesis of zeolite and its regeneration for adsorption of ammonia nitrogen in water
This study presents a novel green approach for the preparation of zeolite material from fly ash using a combination of mechanochemical method. Compared to traditional methods, this approach reduces energy consumption, minimizes reagent usage, and facilitates the efficient recycling of fly ash. The physicochemical properties of the synthesized zeolite, including crystal structure and porosity, were systematically investigated. The synthesized zeolite was employed for the adsorption of ammonia nitrogen from aqueous solutions, and their adsorption kinetics and thermodynamics were comprehensively studied. The results revealed that the adsorption of ammonia nitrogen onto the zeolite follows the Langmuir adsorption model. Additionally, the zeolite exhibited strong selective adsorption and remarkable resistance to interference from coexisting cations in the aqueous solution. Finally, regeneration experiments were conducted using NaCl, NaClO, and their mixtures to desorb ammonia nitrogen from the spent zeolite. A total of 17 regeneration cycles were performed until the adsorption capacity of the zeolites was exhausted. The adsorption performance of the regenerated zeolite was evaluated to assess the impact of different reagents and regeneration cycles on adsorption efficiency. The optimal regeneration method was identified, leading to the successful valorization of fly ash into zeolite for ammonia adsorption and the development of effective regeneration strategies for spent zeolite.
- 4 October 2024
- Published by Springer Nature in Research Square
Open AccessGreen synthesis of zeolite and its regeneration for adsorption of ammonia nitrogen in water
This study presents a novel green approach for the preparation of zeolite material from fly ash using a combination of mechanochemical method. Compared to traditional methods, this approach reduces energy consumption, minimizes reagent usage, and facilitates the efficient recycling of fly ash. The physicochemical properties of the synthesized zeolite, including crystal structure and porosity, were systematically investigated. The synthesized zeolite was employed for the adsorption of ammonia nitrogen from aqueous solutions, and their adsorption kinetics and thermodynamics were comprehensively studied. The results revealed that the adsorption of ammonia nitrogen onto the zeolite follows the Langmuir adsorption model. Additionally, the zeolite exhibited strong selective adsorption and remarkable resistance to interference from coexisting cations in the aqueous solution. Finally, regeneration experiments were conducted using NaCl, NaClO, and their mixtures to desorb ammonia nitrogen from the spent zeolite. A total of 17 regeneration cycles were performed until the adsorption capacity of the zeolites was exhausted. The adsorption performance of the regenerated zeolite was evaluated to assess the impact of different reagents and regeneration cycles on adsorption efficiency. The optimal regeneration method was identified, leading to the successful valorization of fly ash into zeolite for ammonia adsorption and the development of effective regeneration strategies for spent zeolite.
- 9 April 2024
- Published by American Chemical Society (ACS) in ACS Applied Materials & Interfaces
- Vol. 16 (15) , 18671-18685
Ball Milling of La2O3 Tailors the Crystal Structure, Reactive Oxygen Species, and Free Radical and Non-Free Radical Photocatalytic Pathways
Non-free radical photocatalysis with metal oxide catalysts is an important advanced oxidation process that enables the removal of various emerging environmental pollutants, such as tetracycline. Here, four hexagonal La2O3 photocatalysts with different densities of oxygen vacancy and crystalline features are synthesized and then further treated by ball milling. Ball milling of these La2O3 photocatalysts is found to increase the amount of oxygen vacancies on their surfaces and thereby the amount of 1O2 species produced by them. The photocatalytic degradation of TC by these La2O3 photocatalysts depends on the oxygen vacancies present on them. Furthermore, the ones with a strong (101) diffraction peak remove tetracycline from water systems largely with 1O2 and •OH species, whereas those with a weak (101) diffraction peak do so mainly via 1O2 and direct electron transfer (DET) process. Their overall catalytic properties are also studied by density functional theory calculations. Moreover, the organic products produced from tetracycline by La2O3 photocatalysts containing a strong (101) diffraction peak are found to be less toxic than those produced by La2O3 photocatalysts containing a weak (101) diffraction peak. This study also provides convincing evidence that the structures of La2O3 determine the species that is produced by it and that end up mediating photocatalytic reaction pathways (i.e., free radical versus non-free radical) to degrade an emerging environment pollutant.
- 9 April 2024
- Published by American Chemical Society (ACS) in ACS Applied Materials & Interfaces
- Vol. 16 (15) , 18671-18685
Ball Milling of La2O3 Tailors the Crystal Structure, Reactive Oxygen Species, and Free Radical and Non-Free Radical Photocatalytic Pathways
Non-free radical photocatalysis with metal oxide catalysts is an important advanced oxidation process that enables the removal of various emerging environmental pollutants, such as tetracycline. Here, four hexagonal La2O3 photocatalysts with different densities of oxygen vacancy and crystalline features are synthesized and then further treated by ball milling. Ball milling of these La2O3 photocatalysts is found to increase the amount of oxygen vacancies on their surfaces and thereby the amount of 1O2 species produced by them. The photocatalytic degradation of TC by these La2O3 photocatalysts depends on the oxygen vacancies present on them. Furthermore, the ones with a strong (101) diffraction peak remove tetracycline from water systems largely with 1O2 and •OH species, whereas those with a weak (101) diffraction peak do so mainly via 1O2 and direct electron transfer (DET) process. Their overall catalytic properties are also studied by density functional theory calculations. Moreover, the organic products produced from tetracycline by La2O3 photocatalysts containing a strong (101) diffraction peak are found to be less toxic than those produced by La2O3 photocatalysts containing a weak (101) diffraction peak. This study also provides convincing evidence that the structures of La2O3 determine the species that is produced by it and that end up mediating photocatalytic reaction pathways (i.e., free radical versus non-free radical) to degrade an emerging environment pollutant.