Photocatalytic activity of NiS, NiO and coupled NiS–NiO for degradation of pharmaceutical pollutant cephalexin under visible light?
RSC Advances Pub Date: 2017-11-28 DOI: 10.1039/C7RA09461B
Abstract
In this research, a magnetic core–shell catalyst support was prepared by polymerization of pyrrole in the presence of Fe3O4 nanoparticles. The magnetic support was employed for the implementation of NiS, NiO and coupled NiS–NiO. The synthesized photocatalysts were characterized by FTIR, TG, XRD, DRS, BET, TEM and SEM techniques and then used for the degradation of pharmaceutical pollutant cephalexin under visible light irradiation. The results indicated that the efficiency of the coupled photocatalyst (Fe3O4@PPY–NiO–NiS) was considerably higher than that of Fe3O4@PPY–NiO and Fe3O4@PPY–NiS. This can be explained by the lower band gap energy of the photocatalysts, obtained after coupling and immobilization on the support. Magnetization of the photocatalyst evaluated by VSM technique showed that the magnetized photocatalyst properly and quickly separated from the reaction solution with the aid of an external magnetic field. Upon regeneration, the photocatalyst retained most of its initial efficiency. The enhancing effect of H2O2 and the inhibition effects of some reagents on the degradation efficiency were studied. The photodegradation products were identified by GC-MS technique.
Recommended Literature
- [1] An arsenic trioxide nanoparticle prodrug (ATONP) potentiates a therapeutic effect on an aggressive hepatocellular carcinoma model via enhancement of intratumoral arsenic accumulation and disturbance of the tumor microenvironment? Xin Fu,Qing-rong Liang,Rong-guang Luo,Yan-shu Li,Xiao-ping Xiao,Lu-lu Yu,Wen-zhe Shan,Guang-qin FanJ. Mater. Chem. B, 2019,7, 3088-3099 10.1039/C9TB00349E
- [2] An artificial CO-releasing metalloprotein built by histidine-selective metallation? Inês S. Albuquerque,Hélia F. Jeremias,Miguel Chaves-Ferreira,Dijana Matak-Vinkovic,Omar Boutureira,Carlos C. Rom?oChem. Commun., 2015,51, 3993-3996 10.1039/C4CC10204E
- [3] An approach to the structure and vibrational analysis of cis- and trans-3-chlorostyrene through IR/Raman and INS spectroscopies and theoretical ab initio/DFT calculations? J. M. Granadino-Roldán,M. Fernández-Gómez,A. Navarro,T. Pe?a Ruiz,U. A. JayasooriyaPhys. Chem. Chem. Phys., 2004,6, 1133-1143 10.1039/B314243D
- [4] An assay for the enzyme N-acetyl-β-d-glucosaminidase (NAGase) based on electrochemical detection using screen-printed carbon electrodes (SPCEs) R. M. Pemberton,J. P. Hart,T. T. MottramAnalyst, 2001,126, 1866-1871 10.1039/B104874K
- [5] An atom-economical protocol for direct conversion of Baylis–Hillman alcohols to β-chloro aldehydes in water? Raktani Bikshapathi,Sai Prathima Parvathaneni,Vaidya Jayathirtha RaoGreen Chem., 2017,19, 4446-4450 10.1039/C7GC01483J
- [6] An amino group functionalized metal–organic framework as a luminescent probe for highly selective sensing of Fe3+ ions? Zhonghua Xiang,Chuanqi Fang,Sanhua Leng,Dapeng CaoJ. Mater. Chem. A, 2014,2, 7662-7665 10.1039/C4TA00313F
- [7] An antioxidant self-healing hydrogel for 3D cell cultures? Lei Yang,Yuan Zeng,Haibo Wu,Chunwu Zhou,Lei TaoJ. Mater. Chem. B, 2020,8, 1383-1388 10.1039/C9TB02792K
- [8] An artificial blood vessel implanted three-dimensional microsystem for modeling transvascular migration of tumor cells? Xue-Ying Wang,Ying Pei,Min Xie,Zi-He Jin,Ya-Shi Xiao,Yang Wang,Li-Na Zhang,Yan Li,Wei-Hua HuangLab Chip, 2015,15, 1178-1187 10.1039/C4LC00973H
- [9] Alternative donor substrates for inverting and retaining glycosyltransferases? Luke L. Lairson,Warren W. WakarchukChem. Commun., 2007, 365-367 10.1039/B614636H
- [10] An integrated system for field analysis of Cd(ii) and Pb(ii) via preconcentration using nano-TiO2/cellulose paper composite and subsequent detection with a portable X-ray fluorescence spectrometer? Xiaofeng LinRSC Adv., 2016,6, 9002-9006 10.1039/C5RA25693C
Journal Name:RSC Advances
research_products
-
CAS no.: 89640-58-4