Multifunctional and recyclable TiO2 hybrid sponges for efficient sorption, detection, and photocatalytic decomposition of organic pollutants

被引:18
|
作者
Lee, Yunjeong [1 ]
Lee, Seungki [1 ]
Kim, Hyo Sil [1 ]
Moon, Jong Tae [2 ]
Joo, Ji Bong [2 ]
Choi, Inhee [1 ]
机构
[1] Univ Seoul, Dept Life Sci, Seoul 02504, South Korea
[2] Konkuk Univ, Dept Chem Engn, Seoul 05029, South Korea
基金
新加坡国家研究基金会;
关键词
TiO2 hybrid sponge; Organic pollutants; Efficient; Sorption; Raman detection; Photocatalytic decomposition; ENHANCED RAMAN-SPECTROSCOPY; ACTIVATED CARBON-FIBERS; RELATIVE-HUMIDITY; SURFACE-CHEMISTRY; MESOPOROUS SILICA; TITANIUM-DIOXIDE; METHYLENE-BLUE; HEAVY-METALS; ADSORPTION; TOLUENE;
D O I
10.1016/j.jiec.2019.02.001
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Developing techniques for monitoring and removing organic pollutants such as solvents and dyes in environmental media is a very important task nowadays. To get rid of the pollutants, efficient materials that can sorb, detect, and decompose such compounds have been consistently sought after. Herein, we demonstrate a simple and inexpensive method to fabricate eco-friendly multifunctional and recyclable TiO2 hybrid sponges composed of a polydimethylsiloxane (PDMS) network and functional nanoparticles. Water-soluble crystals were used to construct porous templates and TiO2 nanoparticles were additionally integrated into the templates where liquid PDMS was filled. After curing the PDMS, the TiO2 integrated hybrid sponges were finally obtained by dissolving the templates with water. By using the fabricated hybrid sponges, sorbed organic pollutants were qualitatively detected via molecular-specific Raman signals. Furthermore, we showed the recyclability by achieving photocatalytic decomposition of the sorbed pollutants induced by the TiO2 nanoparticles. These results are instructive for further applications and also contribute toward solving problems relating to environmental pollution. (C) 2019 The Korean Society of Industrial and Engineering Chemistry. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:328 / 335
页数:8
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