scholarly journals Plasma-Catalysis for Volatile Organic Compounds Decomposition: Complexity of the Reaction Pathways during Acetaldehyde Removal

Catalysts ◽  
2020 ◽  
Vol 10 (10) ◽  
pp. 1146
Author(s):  
Arlette Vega-González ◽  
Xavier Duten ◽  
Sonia Sauce

Acetaldehyde removal was carried out using non-thermal plasma (NTP) at 150 J·L−1, and plasma-driven catalysis (PDC) using Ag/TiO2/SiO2, at three different input energies—70, 350 and 1150 J·L−1. For the experimental configuration used, the PDC process showed better results in acetaldehyde (CH3CHO) degradation. At the exit of the reactor, for both processes and for all the used energies, the same intermediates in CH3CHO decomposition were identified, except for acetone which was only produced in the PDC process. In order to contribute to a better understanding of the synergistic effect between the plasma and the catalyst, acetaldehyde/catalyst surface interactions were studied by diffuse-reflectance infrared Fourier transform spectroscopy (DRIFTS). These measurements showed that different species such as acetate, formate, methoxy, ethoxy and formaldehyde are present on the surface, once it has been in contact with the plasma. A reaction pathway for CH3CHO degradation is proposed taking into account all the identified compounds in both the gas phase and the catalyst surface. It is very likely that in CH3CHO degradation the presence of methanol, one of the intermediates, combined with oxygen activation by silver atoms on the surface, are key elements in the performance of the PDC process.

2018 ◽  
Vol 8 (4) ◽  
pp. 936-954 ◽  
Author(s):  
Xinxin Feng ◽  
Hongxia Liu ◽  
Chi He ◽  
Zhenxing Shen ◽  
Taobo Wang

Non-thermal plasma catalysis with high efficiency, high by-product selectivity and superior carbon balance is one of the most promising technologies in the control of volatile organic compounds (VOCs).


Catalysts ◽  
2019 ◽  
Vol 9 (1) ◽  
pp. 98 ◽  
Author(s):  
Savita K. P. Veerapandian ◽  
Nathalie De Geyter ◽  
Jean-Marc Giraudon ◽  
Jean-François Lamonier ◽  
Rino Morent

Non-thermal plasma technique can be easily integrated with catalysis and adsorption for environmental applications such as volatile organic compound (VOC) abatement to overcome the shortcomings of individual techniques. This review attempts to give an overview of the literature about the application of zeolite as adsorbent and catalyst in combination with non-thermal plasma for VOC abatement in flue gas. The superior surface properties of zeolites in combination with its excellent catalytic properties obtained by metal loading make it an ideal packing material for adsorption plasma catalytic removal of VOCs. This work highlights the use of zeolites for cyclic adsorption plasma catalysis in order to reduce the energy cost to decompose per VOC molecule and to regenerate zeolites via plasma.


2010 ◽  
Vol 1260 ◽  
Author(s):  
Moazzam Ali ◽  
Marty D. Donakowski ◽  
Markus Winterer

AbstractChemical Vapor Functionalization (CVF) is a method in which nanocrystals undergo in situ functionalization in the gas phase. In CVF, two reactors are used in series. The first reactor consists of a hot quartz tube (1073 K) where ZnO nanocrystals are synthesized in the gas phase from diethylzinc and oxygen. The second reactor, connected at the exit of the first one and kept at lower temperature (673 K), is used as functionalization chamber. At the connecting point of the two reactors, vapors of organic functionalizing agents are injected which react with the surface of ZnO nanocrystals. ZnO nanocrystals have been functionalized by 1-hexanol, n-hexanoic acid, n-hexanal and 1-hexylamine. Functionalized ZnO nanocrystals have been characterized by Dynamic Light Scattering, X-ray Diffraction and Diffuse Reflectance Infrared Fourier Transform Spectroscopy.


2019 ◽  
Vol 63 (3-4) ◽  
pp. 394-402 ◽  
Author(s):  
Laura Abis ◽  
Nikolaos Dimitritatos ◽  
Meenakshisundaram Sankar ◽  
Simon J. Freakley ◽  
Graham J. Hutchings

Abstract The oxidation of glycerol represents both a viable route to catalytic upgrading of biomass and has become a model reaction for catalytic polyol oxidation. Gold and gold–palladium nanoparticle catalysts prepared by colloidal methods involving polymer additives have been extensively studied. However, the effect of residual polymer at the catalyst surface on reaction pathways has not been decoupled from particle size effects. We show that when using catalysts prepared without polymer stabilisers the addition of either polyvinyl alcohol or polyvinylpyrrolidone to the reaction changes the reaction rate and results in a change in reaction selectivity. We conclude that the polymer additive has a significant effect on the reaction pathway and that these systems should be considered as a metal surface–polymer interface catalytic systems and properties should not be rationalised solely based on nanoparticle size. Graphic Abstract


2008 ◽  
Vol 2008 ◽  
pp. 1-9 ◽  
Author(s):  
William Balcerski ◽  
Su Young Ryu ◽  
Michael R. Hoffmann

Diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) was used to study illuminatedTiO2surfaces under both vacuum conditions, and in the presence of organic molecules (decane and methanol). In the presence of hole scavengers, electrons are trapped at Ti(III)–OH sites, and free electrons are generated. These free electrons are seen to decay by exposure either to oxygen or to heat; in the case of heating, reinjection of holes into the lattice by loss of sorbed hole scavenger leads to a decrease in Ti(III)–OH centers. Decane adsorption experiments lend support to the theory that removal of surficial hydrocarbon contaminants is responsible for superhydrophilicTiO2surfaces. Oxidation of decane led to a mixture of surface-bound organics, while oxidation of methanol leads to the formation of surface-bound formic acid.


1993 ◽  
Vol 47 (11) ◽  
pp. 1760-1766 ◽  
Author(s):  
J. J. Benitez ◽  
I. Carrizosa ◽  
J. A. Odriozola

In this work the experimental details and some examples of applications of diffuse reflectance infrared technique are described. Special interest has been devoted to a correct determination of the temperature of the sample, to gas-phase analysis, and to quantitative aspects in a DRIFTS controlled environmental cell. Applications to the analysis of the gas phase during catalytic hydrogenation and to the obtainment of kinetic parameters for the catalytic decomposition of adsorbates are included.


2018 ◽  
Vol 22 (2) ◽  
pp. 73-94 ◽  
Author(s):  
Bangfen Wang ◽  
Xiaoxin Xu ◽  
Weicheng Xu ◽  
Ni Wang ◽  
Hailin Xiao ◽  
...  

Author(s):  
Hasan Masitah ◽  
Toshiki Asakoshi ◽  
Hiroki Muroyama ◽  
Toshiaki Matsui ◽  
Koichi Eguchi

Supported Ni catalysts are active in CO2 methanation. To understand the reaction mechanism is important for the development of highly-active catalysts. In this study, we investigated the reaction pathways of...


2017 ◽  
Vol 7 (24) ◽  
pp. 5932-5943 ◽  
Author(s):  
Chaoquan Hu ◽  
Jiahan Sun ◽  
Yafeng Yang ◽  
Qingshan Zhu ◽  
Bin Yu

The reaction pathway for partial hydrogenation of 1,3-butadiene over a Pt/SiO2 catalyst was explored with a combination of in situ diffuse reflectance infrared Fourier transform (DRIFT) spectroscopy, intrinsic kinetics, and density functional theory (DFT) calculations.


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