0 Datasets
0 Files
Get instant academic access to this publication’s datasets.
Yes. After verification, you can browse and download datasets at no cost. Some premium assets may require author approval.
Files are stored on encrypted storage. Access is restricted to verified users and all downloads are logged.
Yes, message the author after sign-up to request supplementary files or replication code.
Join 50,000+ researchers worldwide. Get instant access to peer-reviewed datasets, advanced analytics, and global collaboration tools.
✓ Immediate verification • ✓ Free institutional access • ✓ Global collaborationJoin our academic network to download verified datasets and collaborate with researchers worldwide.
Get Free AccessAbstract The degradation effects and mechanism on gemfibrozil (GEM) in aqueous solution by dielectric barrier discharge (DBD) plasma combined with the catalyst CNTs/γFe 2 O 3 are investigated. The concentrations of plasma‐generated reactive species, including H 2 O 2 , O 3 , , and OH, are measured with spectrophotometric and fluorescent probes. The effects of the plasma treatment period, discharge power, initial GEM concentration, solution pH value, conductivity, and the catalytic property are studied on the degradation rate and energy efficiency. Compared with the sole plasma treatment, CNTs/γFe 2 O 3 could maximally improve the GEM degradation rate and energy efficiency to 99.7% ± 0.2% and 76.5 ± 5.2 mg·kW −1 ·h −1 , respectively. The solution's total organic carbon removal efficiency has been increased to 47.2% ± 2.7%. Meanwhile, the possible degradation pathways of the plasma‐treated GEM solution and overall biological toxicity of GEM degradation intermediates and residual catalyst in solution are investigated.
Zimu Xu, Bin Zhu, Zhengxin Ye, Nannan Zhang, Jie Shen, Lan Yan, Shuheng Hu, Cheng Cheng, Yunxia Li, Fan Yang, Paul Kim Ho Chu (2021). Degradation of gemfibrozil in aqueous solutions by gas–liquid dielectric barrier discharge plasma combined with CNTs/γFe<sub>2</sub>O<sub>3</sub>. , 19(3), DOI: https://doi.org/10.1002/ppap.202100122.
Datasets shared by verified academics with rich metadata and previews.
Authors choose access levels; downloads are logged for transparency.
Students and faculty get instant access after verification.
Type
Article
Year
2021
Authors
11
Datasets
0
Total Files
0
Language
en
DOI
https://doi.org/10.1002/ppap.202100122
Access datasets from 50,000+ researchers worldwide with institutional verification.
Get Free Access