A facile and green synthetic approach toward fabrication of Alcea- and Thyme-stabilized TiO2 nanoparticles for photocatalytic applications

被引:26
作者
Arabi, Negar [1 ]
Kianvash, Abbas [1 ]
Hajalilou, Abdollah [1 ]
Abouzari-Lotf, Ebrahim [2 ,3 ]
Abbasi-Chianeh, Vahid [4 ]
机构
[1] Tabriz Univ, Dept Mat Engn, Fac Mech Engn, Tabriz, Iran
[2] Univ Teknol Malaysia, Ctr Hydrogen Energy, Adv Mat Res Grp, Kuala Lumpur 54100, Malaysia
[3] Univ Teknol Malaysia, Dept Chem Engn, Johor Baharu 81310, Malaysia
[4] Urmia Univ Technol, Fac Min & Mat Engn, Orumiyeh, Iran
关键词
TiO(2)nanoparticles; Green synthesis; Photocatalytic properties; NANOCRYSTALLINE TIO2; DEGRADATION; RUTILE; HETEROSTRUCTURE; ANATASE; SURFACE;
D O I
10.1016/j.arabjc.2018.03.014
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A facile and green synthetic approach was considered for the synthesis of stabilized titanium dioxide (TiO2) nanoparticles. Extracts of Alcea and Thyme plants were used to synthesis TiO2 nanoparticles for photocatalytic applications. Evaluation of the structural and phase formation via X-ray diffraction (XRD) indicated the formation of the anatase phase of TiO2 along with the rutile phase. A desired single phase of anatase was obtained upon heating the as-synthesized samples at 500 degrees C for 3 h. Using the information provided by the XRD analyzer and the Debye Scherer relationship, the average crystallite size was found to be around 6 and 10 nm for the samples synthesized using Alcea and Thyme plants, respectively. To determine the elemental analysis and chemical structure, the energy dispersive X-ray (EDX) analyzer and Fourier Transform Infrared (FTIR) spectroscopy were employed. Field emission scanning electron microscopy (FESEM) indicated batches of ultrafine agglomerated particles for both samples, which their sizes grew by the heating process. The UV-visible analysis of photocatalytic properties confirmed the priority of TiO2 nanoparticles prepared with Thyme extracts. (C) 2018 Production and hosting by Elsevier B.V. on behalf of King Saud University.
引用
收藏
页码:2132 / 2141
页数:10
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