ZnO/ZrO2 nanocomposite: Sonosynthesis, characterization and its application for wastewater treatment

被引:70
作者
Aghabeygi, Shokufeh [1 ]
Khademi-Shamami, Mostafa [1 ]
机构
[1] Islamic Azad Univ, East Tehran Branch, Dept Chem, Tehran, Iran
关键词
Photodegradation; Ultrasonic irradiation; ZnO/ZrO2; nanocomposite; Wastewater treatment; PHOTOCATALYTIC DEGRADATION; PHENOL-PHOTODEGRADATION; OPTICAL-PROPERTIES; METHYLENE-BLUE; REMOVAL; NANO; NANOPARTICLES; PERFORMANCE; MECHANISM; DECOLORIZATION;
D O I
10.1016/j.ultsonch.2017.09.020
中图分类号
O42 [声学];
学科分类号
070206 ; 082403 ;
摘要
ZnO/ZrO2 nanocomposites with different ZnO: ZrO2 molar ratios (2:1, 1:1, and 1:2)were prepared by sol gel approach under ultrasonic irradiation. For preparation of the nano-composites, the ZnO gel was directly incorporated into the ZrO2 gel at different molar ratios. The reaction mixture was stirred continuously for two days and then it was ultrasonoicated for 30 min. The filtrated composite gel was washed, and then calcinated at 300 degrees C in furnace for 3 h. X-ray powder diffraction patterns exhibited well-formed crystal structures and pure crystalline phases in the synthesized nanoparticles (NPs). The FT-IR analyses indicated that the positions of peaks related to Zn-O and Zr-O absorption bands did not change in nano-composites. In addition, FESEM images indicated uniform spherical morphology of the NPs. The highest photo-degradation performance of Congo red (as a model water pollutant) was obtained by 1:2molar ratio of ZrO2: ZnO in the nano-composite. The particle size and band gap were considered as important factors on nano-catalysts performance. Furthermore, the effects of ultrasonic irradiation, pH, and the concentration of pollutant in solution were investigated on photocatalytic performance of optimum nanocomposite.
引用
收藏
页码:458 / 465
页数:8
相关论文
共 45 条
[1]   Photocatalytic degradation of indigo carmine using [Zn-Al] LDH supported on PAN nanofibres [J].
Abderrazek, K. ;
Uheida, A. ;
Seffen, M. ;
Muhammed, M. ;
Srasra, N. Frini ;
Srasra, E. .
CLAY MINERALS, 2015, 50 (02) :185-197
[2]  
Agli G.D., 2000, J EUR CERAM SOC, V20, P139
[3]   Photocatalytic, sonocatalytic and sonophotocatalytic degradation of Rhodamine B using ZnO/CNTs composites photocatalysts [J].
Ahmad, M. ;
Ahmed, E. ;
Hong, Z. L. ;
Ahmed, W. ;
Elhissi, A. ;
Khalid, N. R. .
ULTRASONICS SONOCHEMISTRY, 2014, 21 (02) :761-773
[4]   Core-shell structured epoxide functional NiO/SiO2 nanocomposite particles and photocatalytic decolorization of congo red aqueous solution [J].
Akhtar, Mosammat Sammi ;
Alam, Mohammad Ashraful ;
Tauer, Klaus ;
Hossan, Mohammad Shamim ;
Sharafat, Mostafa Kaiyum ;
Rahman, Mohammad Mahbubor ;
Minami, Hideto ;
Ahmad, Hasan .
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS, 2017, 529 :783-792
[5]  
Akl AA, 2016, CHALCOGENIDE LETT, V13, P247
[6]   Effect of Mn doping on the structural and optical properties of sol-gel derived ZnO nanoparticles [J].
Ali, Abdub G. ;
Dejene, Francis B. ;
Swart, Hendrik C. .
CENTRAL EUROPEAN JOURNAL OF PHYSICS, 2012, 10 (02) :478-484
[7]   A comparative adsorption study with different industrial wastes as adsorbents for the removal of cationic dyes from water [J].
Bhatnagar, A ;
Jain, AK .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 2005, 281 (01) :49-55
[8]   Synthesis and application of multiple rods gold-zinc oxide nanostructures in the photocatalytic degradation of methyl orange [J].
Chamjangali, M. Arab ;
Bagherian, G. ;
Bahramian, B. ;
Rad, B. Fahimi .
INTERNATIONAL JOURNAL OF ENVIRONMENTAL SCIENCE AND TECHNOLOGY, 2015, 12 (01) :151-160
[9]   Photocatalytic degradation of CI Acid Orange 52 in the presence of Zn-doped TiO2 prepared by a stearic acid gel method [J].
Chen, Cheng ;
Wang, Zhuyi ;
Ruan, Shengping ;
Zou, Bo ;
Zhao, Meng ;
Wu, Fengqing .
DYES AND PIGMENTS, 2008, 77 (01) :204-209
[10]   Preparation of ZnO/GO composite material with highly photocatalytic performance via an improved two-step method [J].
Chen, Ya-Li ;
Zhang, Chun-E ;
Deng, Chao ;
Fei, Peng ;
Zhong, Ming ;
Su, Bi-Tao .
CHINESE CHEMICAL LETTERS, 2013, 24 (06) :518-520