Abstract:Multi-structured Ag/MnO
2
-cordierite molded catalysts were prepared by hydrothermal method and applied to the catalytic oxidation of VOCs. Catalytic activities of Ag/MnO
2
-cordierite were evaluated by 1000 ppm of toluene, ethyl acetate and chlorobenzene degradation respectively at the air atmosphere, and their physicochemical properties were characterized through multiple techniques containing XRD, SEM, TEM, H
2
-TPR and XPS. It is found th… Show more
“…The effect of various supports on the catalytic performance of loaded Ag catalysts for VOC oxidation has been investigated extensively. 190–192 For example, Zhao et al 193 synthesized the white graphene foam supported Ag catalyst, over which an excellent performance ( T 90 = 110 °C for methanol), almost half of the T 90 obtained over Ag/γ-Al 2 O 3 , was observed. The superior activity originated from the unique multilayer pore structure and the atomic thin-walled layer of white graphene foam, which favored stabilizing the supported Ag species.…”
Section: Snmcs For Voc Catalytic Oxidationmentioning
confidence: 99%
“…The effect of various supports on the catalytic performance of loaded Ag catalysts for VOC oxidation has been investigated extensively. [190][191][192] For example, Zhao et al 193 184 Copyright 2014 American Chemical Society. (B) HCHO catalytic performance of pure SiO 2 particles and Au particles.…”
Section: Catalysis Science and Technologymentioning
Volatile organic compounds (VOCs), one type of pollutant which not only causes a series of environmental issues but does extreme harm to human health, have attracted extensive attention. Therefore, it...
“…The effect of various supports on the catalytic performance of loaded Ag catalysts for VOC oxidation has been investigated extensively. 190–192 For example, Zhao et al 193 synthesized the white graphene foam supported Ag catalyst, over which an excellent performance ( T 90 = 110 °C for methanol), almost half of the T 90 obtained over Ag/γ-Al 2 O 3 , was observed. The superior activity originated from the unique multilayer pore structure and the atomic thin-walled layer of white graphene foam, which favored stabilizing the supported Ag species.…”
Section: Snmcs For Voc Catalytic Oxidationmentioning
confidence: 99%
“…The effect of various supports on the catalytic performance of loaded Ag catalysts for VOC oxidation has been investigated extensively. [190][191][192] For example, Zhao et al 193 184 Copyright 2014 American Chemical Society. (B) HCHO catalytic performance of pure SiO 2 particles and Au particles.…”
Section: Catalysis Science and Technologymentioning
Volatile organic compounds (VOCs), one type of pollutant which not only causes a series of environmental issues but does extreme harm to human health, have attracted extensive attention. Therefore, it...
“…3(a. [1][2][3] shows the morphology of a CNT element which was fabricated by coating a glass-fiber textile specimen with CNTs. CNTs are densely packed on the surface of the glass-fiber textile, as observed in the high-resolution FE-SEM image in Fig.…”
Section: Morphological and Electrical Characteristicsmentioning
confidence: 99%
“…Recently, various studies have been conducted that explore methods to reduce fine dust as increasing fine dust concentrations in the environment have become a serious global concern. Volatile organic compounds (VOCs) are one of the main fine dust precursors and contribute significantly to the generation of fine dust [1]. VOCs are emitted by various solids and liquids in our living and working environments and high concentrations or long-term exposure pose a significant health risk [2].…”
“…VOCs are emitted by various solids and liquids in our living and working environments and high concentrations or long-term exposure pose a significant health risk [2]. Methods investigated to reduce VOCs involve adsorption [3][4][5][6], photocatalytic decomposition [7,8], catalytic oxidation [1,2,[9][10][11][12][13][14][15], and non-thermal plasma. A disadvantage of adsorption methods is the necessity for the periodic post-process treatment of spent adsorbents involving the desorption of captured VOCs or regeneration of the adsorbent [16,17].…”
A thermal catalytic device that reduces the energy required for the catalytic oxidation of volatile organic compounds (VOCs) was developed. The catalytic oxidation of VOCs is typically performed under indirect heating conditions resulting in high energy consumption. The proposed device drastically decreases the energy consumed and increases the amount of toluene decomposed during catalytic oxidation because the catalysts are heated directly via a carbon nanotube (CNT) element. The proposed device consists of a glass-fiber textile coated in CNTs, α-MnO2 nanostructures, and Pt nanostructures. The effect of different α-MnO2 nanostructures (granular and urchin-like) on device performance was investigated. Moreover, the effect of each device component on the toluene decomposition efficiency and energy consumption of the device was explored by determining the toluene concentration of gaseous toluene after the catalytic oxidation process and the associated energy consumption. The device featuring urchin-like α-MnO2 nanostructures coated in a thin layer of Pt achieves higher toluene decomposition efficiency than the device featuring granular α-MnO2 nanostructures coated in Pt nanoparticles. Moreover, the device featuring urchin-like α-MnO2 nanostructures coated in a thin Pt layer achieves higher toluene decomposition efficiency and lower energy consumption under direct heating conditions than under conventional indirect heating conditions.
Hopcalite supported Ag (wt.%: 0.5; 1; 2; 10)‐containing materials were prepared by wet impregnation followed by calcination at 400 °C for adsorption‐thermal catalytic oxidation of toluene. Based on breakthrough experiments, the duration of the adsorption step was set around 38 min to minimize toluene loss at the outlet of the reactor (<3 mol% of the amount of toluene adsorbed) allowing to determine a dynamic useful adsorption capacity for toluene. Thermal oxidation was performed in a He : O2 (75 : 25) gaseous mixture from 20 °C to 250 °C (90 min) to assess the catalytic properties of the bifunctional materials throughout on‐line monitoring of unreacted toluene and CO2 during the temperature programmed reaction. Hop‐0.5 Ag exhibited the best performance with a CO2 yield of 98.9 %. Excellent redox properties and minimization of thermal effects were invoked to enhance total oxidation of toluene. Additionally, these bifunctional materials showed good stability under cycling conditions.
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