Ultrasound to improve both synthesis and pollutants degradation based on metal nanoparticles supported on TiO2

被引:25
作者
Stucchi, M. [1 ]
Cerrato, G. [2 ]
Bianchi, C. L. [1 ,3 ]
机构
[1] Univ Milan, Chem Dept, Via Golgi 19, I-20133 Milan, Italy
[2] Univ Turin, Chem Dept, Via P Giuria 7, I-10125 Turin, Italy
[3] Consorzio INSTM, Florence, Italy
关键词
Metal NPs; Photocatalysis; Ultrasound; Water remediation; Drugs degradation; Air purification; SONOCHEMICAL SYNTHESIS; ASSISTED SYNTHESIS; TITANIUM-DIOXIDE; PHOTOCATALYTIC ACTIVITY; WATER; CU; OXIDATION; NANO;
D O I
10.1016/j.ultsonch.2018.07.011
中图分类号
O42 [声学];
学科分类号
070206 ; 082403 ;
摘要
Sonochemistry is based on acoustic cavitation, which consist in the formation, growth, and implosive collapse of bubbles within a liquid. Collapsing bubbles generate localized hot spots, characterized by temperatures up to 5000 K and pressures up to 1800 atm. These extreme conditions allow producing a variety of nanostructured and amorphous materials, as well as they are advantageous for chemical processes. Ultrasound requires inexpensive equipment and fewer steps than conventional methods. Combining ultrasound and photocatalysis enhances the performance of the processes, reduces reaction time, avoids the use of extreme physical conditions and improves the photocatalytic materials properties increasing their activity. Here, we reported the positive effect of US in synthesizing Me-modified TiO2 (Me = Ag, Cu, Mn) for pollutants degradation in gas-phase; also, we proved the advantageous application of ultrasound for the photocatalytic removal of organic compounds in water. Ultrasound produced more efficient Me-doped TiO2, which showed higher activity in visible light. When combined with photocatalytic water treatment, the organic compounds degradation and mineralization increases.
引用
收藏
页码:462 / 468
页数:7
相关论文
共 40 条
[1]   Sonochemistry in environmental remediation. 2. Heterogeneous sonophotocatalytic oxidation processes for the treatment of pollutants in water [J].
Adewuyi, YG .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2005, 39 (22) :8557-8570
[2]   Cu/TiO2 photocatalysts for the conversion of acetic acid into biogas and hydrogen [J].
Amoros-Perez, Ana ;
Cano-Casanova, Laura ;
Angeles Lillo-Rodenas, Maria ;
Carmen Roman-Martinez, M. .
CATALYSIS TODAY, 2017, 287 :78-84
[3]   Photocatalytic degradation of acetone, acetaldehyde and toluene in gas-phase: Comparison between nano and micro-sized TiO2 [J].
Bianchi, C. L. ;
Gatto, S. ;
Pirola, C. ;
Naldoni, A. ;
Di Michele, A. ;
Cerrato, G. ;
Crocella, V. ;
Capucci, V. .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2014, 146 :123-130
[4]   Cu-doped TiO2 systems with improved photocatalytic activity [J].
Colon, G. ;
Maicu, M. ;
Hidalgo, M. C. ;
Navio, J. A. .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2006, 67 (1-2) :41-51
[5]   Mn-doped TiO2 nanopowders with remarkable visible light photocatalytic activity [J].
Deng, Q. R. ;
Xia, X. H. ;
Guo, M. L. ;
Gao, Y. ;
Shao, G. .
MATERIALS LETTERS, 2011, 65 (13) :2051-2054
[6]   Preparation and Characterization of Mn-Doped Titanates with a Bicrystalline Framework: Correlation of the Crystallite Size with the Synergistic Effect on the Photocatalytic Activity [J].
Devi, L. Gomathi ;
Kottam, Nagaraju ;
Kumar, S. Girish .
JOURNAL OF PHYSICAL CHEMISTRY C, 2009, 113 (35) :15593-15601
[7]   Silver colloid nanoparticles: Ultrasound-assisted synthesis, electrical and rheological properties [J].
Goharshadi, Elaheh K. ;
Azizi-Toupkanloo, Hossein .
POWDER TECHNOLOGY, 2013, 237 :97-101
[8]   Nanostructured molybdenum carbide: Sonochemical synthesis and catalytic properties [J].
Hyeon, TH ;
Fang, MM ;
Suslick, KS .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1996, 118 (23) :5492-5493
[9]   Human pharmaceuticals in wastewater treatment processes [J].
Jones, OAH ;
Voulvoulis, N ;
Lester, JN .
CRITICAL REVIEWS IN ENVIRONMENTAL SCIENCE AND TECHNOLOGY, 2005, 35 (04) :401-427
[10]   Sonophotocatalysis in advanced oxidation process: A short review [J].
Joseph, Collin G. ;
Puma, Gianluca Li ;
Bono, Awang ;
Krishnaiah, Duduku .
ULTRASONICS SONOCHEMISTRY, 2009, 16 (05) :583-589