Liumin Luo
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Research Interests
Liumin Luo has a total of 6 co-authors. Here are the top co-authors by number of shared publications:
- Fu-Ren Xiao
Key Lab of Metastable Materials Science & Technology, Hebei Key Lab for Optimizing Metal Product Technology and Performance, College of Materials Science & Engineering, Yanshan University, Qinhuangdao 066004, China
1 shared publication - Jin Li
School of Mechanical and Eletrical Engineering, Zhoukou Normal University, Zhoukou 466000, China
1 shared publication - Xiaodong Zhou
School of Mechanical and Eletrical Engineering, Zhoukou Normal University, Zhoukou 466000, China
1 shared publication - Xiaoyu Zhou
School of Mechanical and Electrical Engineering, ZhouKou Normal University, Zhoukou 466000, China
1 shared publication - Yu Gu
School of Mechanical and Eletrical Engineering, Zhoukou Normal University, Zhoukou 466000, China
1 shared publication - Zhi Li
California State University San Bernardino, 5500 University Pkwy, San Bernardino, CA 92407, USA
1 shared publication
Latest Publications
- Open Access
- 19 December 2019
- Published by MDPI AG in Nanomaterials
- Vol. 10 (1) , 18
Bacterial Disinfection by CuFe2O4 Nanoparticles Enhanced by NH2OH: A Mechanistic Study
Many disinfection technologies have emerged recently in water treatment industry, which are designed to inactivate water pathogens with extraordinary efficiency and minimum side effects and costs. Current disinfection processes, including chlorination, ozonation, UV irradiation, and so on, have their inherent drawbacks, and have been proven ineffective under certain scenarios. Bacterial inactivation by noble metals has been traditionally used, and copper is an ideal candidate as a bactericidal agent owing to its high abundance and low cost. Building on previous findings, we explored the bactericidal efficiency of Cu(I) and attempted to develop it into a novel water disinfection platform. Nanosized copper ferrite was synthesized, and it was reduced by hydroxylamine to form surface bound Cu(I) species. Our results showed that the generated Cu(I) on copper ferrite surface could inactivate E. coli at a much higher efficiency than Cu(II) species. Elevated reactive oxygen species’ content inside the cell primarily accounted for the strong bactericidal role of Cu(I), which may eventually lead to enhanced oxidative stress towards cell membrane, DNA, and functional proteins. The developed platform in this study is promising to be integrated into current water treatment industry.
- 19 December 2019
- Published by MDPI AG in Nanomaterials
- Vol. 10 (1) , 18
Open AccessBacterial Disinfection by CuFe2O4 Nanoparticles Enhanced by NH2OH: A Mechanistic Study
Many disinfection technologies have emerged recently in water treatment industry, which are designed to inactivate water pathogens with extraordinary efficiency and minimum side effects and costs. Current disinfection processes, including chlorination, ozonation, UV irradiation, and so on, have their inherent drawbacks, and have been proven ineffective under certain scenarios. Bacterial inactivation by noble metals has been traditionally used, and copper is an ideal candidate as a bactericidal agent owing to its high abundance and low cost. Building on previous findings, we explored the bactericidal efficiency of Cu(I) and attempted to develop it into a novel water disinfection platform. Nanosized copper ferrite was synthesized, and it was reduced by hydroxylamine to form surface bound Cu(I) species. Our results showed that the generated Cu(I) on copper ferrite surface could inactivate E. coli at a much higher efficiency than Cu(II) species. Elevated reactive oxygen species’ content inside the cell primarily accounted for the strong bactericidal role of Cu(I), which may eventually lead to enhanced oxidative stress towards cell membrane, DNA, and functional proteins. The developed platform in this study is promising to be integrated into current water treatment industry.