Special Issue "Catalytic Combustion"


A special issue of Catalysts (ISSN 2073-4344).

Deadline for manuscript submissions: closed (15 June 2013)

Special Issue Editor

Guest Editor
Dr. Marco J. Castaldi
Chemical Engineering Department, The City College of New York, City University of New York, 140th Street at Convent Avenue, Steinman Hall, Room 307, New York, NY 10031, USA
Website: http://ccllabs.wordpress.com/people/marco-j-castaldi/
E-Mail: mcastaldi@che.ccny.cuny.edu
Phone: +1 212 650 6679
Interests: reforming catalysis; gasification; combustion; reaction engineering; mechanisms

Special Issue Information

Dear Colleagues,

Catalytic combustion has been studied extensively for a variety of catalyst formulations and fuel conversion. In the late 1980’s to early 2000’s catalytic combustion of natural gas was determined to be one of a couple of technologies that can meet ultra-low NOx (i.e., less than 3 ppmV@15% O2) requirements in the power generation industry. The extreme temperature gradients and rapid reaction kinetics are coupled with the requirement to maintain a low pressure thus making the design of the system very challenging. Although the pace of development has slowed recently there is still research continuing primarily due to the attributes associated with catalytic combustion. For example, catalytic combustion enables operation outside the flammability regime and it releases heat directly onto a surface enabling non-conventional heat integration. Furthermore, it has been shown that catalytic combustion has the ability to interrupt the NOx formation pathways and does not allow carbon-based emissions, such as CO and UHC to be released making it a true pollution prevention technique. Finally, there are some very similar performance characteristics with partial oxidation systems. It is anticipated that as synthetic fuels are developed their combustion characteristics will vary yet catalytic combustion may normalize those variations.

This special issue will cover numerous developments in the area of catalytic combustion research.

Prof. Dr. Marco J. Castaldi
Guest Editor


Manuscripts should be submitted online at www.mdpi.com by registering and logging in to this website. Once you are registered, click here to go to the submission form. Manuscripts can be submitted until the deadline. Papers will be published continuously (as soon as accepted) and will be listed together on the special issue website. Research articles, review articles as well as communications are invited. For planned papers, a title and short abstract (about 100 words) can be sent to the Editorial Office for announcement on this website.

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  • catalysis
  • combustion
  • pollution prevention
  • high temperature

Published Papers (4 papers)

Catalysts 2013, 3(4), 774-793; doi:10.3390/catal3040774
Received: 28 June 2013; in revised form: 5 August 2013 / Accepted: 26 September 2013 / Published: 15 October 2013
Show/Hide Abstract | PDF Full-text (2817 KB) | HTML Full-text | XML Full-text

Catalysts 2013, 3(3), 646-655; doi:10.3390/catal3030646
Received: 25 May 2013; in revised form: 10 July 2013 / Accepted: 26 July 2013 / Published: 2 August 2013
Show/Hide Abstract | Cited by 1 | PDF Full-text (1015 KB) | HTML Full-text | XML Full-text

Catalysts 2013, 3(2), 378-400; doi:10.3390/catal3020378
Received: 20 December 2012; in revised form: 16 February 2013 / Accepted: 25 March 2013 / Published: 8 April 2013
Show/Hide Abstract | PDF Full-text (491 KB) | HTML Full-text | XML Full-text

Catalysts 2013, 3(1), 88-103; doi:10.3390/catal3010088
Received: 10 November 2012; in revised form: 13 November 2012 / Accepted: 29 January 2013 / Published: 6 February 2013
Show/Hide Abstract | Cited by 4 | PDF Full-text (720 KB) | HTML Full-text | XML Full-text
abstract graphic

Planned Papers

The below list represents only planned manuscripts. Some of these manuscripts have not been received by the Editorial Office yet. Papers submitted to MDPI journals are subject to peer-review.

Type of Paper: Article
Au/HMS and Au/SBA-15 Catalysts Doped by CeO2: Silica Host Effect on the Structural and Catalytic Properties
L.F. Liotta 1,*, G. Pantaleo 1, F. Puleo 2, E. Caponetti 2,3, A. Spinella 3,G. Marcì 4,5 and A.M. Venezia1
1 Istituto per Lo Studio dei Materiali Nanostrutturati (ISMN)-CNR via Ugo La Malfa, 153, 90146 Palermo, Italy
Dipartimento di Chimica, Università di Palermo, Parco d’Orleans II, Viale delle Scienze Ed.17, Palermo 90128, Italy
Dipartimento di Chimica, Università di Palermo, Parco d’Orleans II, Viale delle Scienze Ed.17, Palermo 90128, Italy
4 Centro Grandi Apparecchiature-UniNetLab,Università di Palermo, via Marini 14, Palermo 90128, Italy
5 Dipartimento di Ingegneria Elettrica, Elettronica, delle Telecomunicazioni, di Tecnologie Chimiche, Automatica e modelli Matematici (DIEETCAM), Ed. 6, Viale delle Scienze, 90128 Palermo
Abstract:In this work the effects of the modification of hexagonal mesoporous silica, SBA-15 and HMS by doping with ceria (5–20 wt%) on the physico-chemical and catalytic properties of Au (1.5 wt%) supported catalysts were evaluated. Characterizations by N2 physisorption, XRD, XPS, SEM and 29Si1H CP-MAS NMR techniques were performed. The catalytic performances were evaluated in the total oxidation of propene, chosen as model VOC molecule. To this aim, catalytic activity tests were carried out in a tubular fixed-bed reactor under the reactive gas mixture containing 1000 ppm of C3H6 and 9% O2 in He. The hexagonally ordered mesoporous structure of SBA-15 played a key role in stabilizing Au particle size and Au-CeO2 interaction, which are the key factors for propene oxidation activity. On the contrary, ceria deposition disturbed the symmetry of the wormhole HMS silica causing poor Au-CeO2 interaction and poor activity for ceria loading >15 wt%.
: SBA-15, HMS; porous structure; Au-CeO2 interaction

Type of Paper: Review
Catalytic Soot Combustion
Vaccaro S. and Palma V.
Department of Industrial Engineering University of Salerno, 84084 Fisciano (SA), Italy
The review will contain the history of this particular application of catalysis with highlights of the relevant developments occurred in the last decades. It will also describe  the experimental techniques employed to study the process, the models proposed and the applications reported in the relevant literature. Further, the paper will outline the limits of such a technology with respect to the needs imposed by the present and future  regulations on the pollutant emissions, enacted to preserve of the quality and the salubrity of the environment.

Type of Paper: Review
Catalytic Combustion for Supplying Energy for Endothermic Reaction
Vaccaro S. and Malangone L.
Department of Industrial Engineering University of Salerno, 84084 Fisciano (SA), Italy
This review will focus on the use of the catalytic combustion of a fuel to supply energy to endothermic reacting systems for performing specific applications for which the compactness and the transportability of the device are essential requirements. It will also regard the possibility to tailor the features of the catalyst to the needs of the endothermic reacting system. It will review the relevant literature regarding micro devices starting with a short general outline of such systems and then focusing on the experimental techniques employed by researchers to study these catalytic reactors and the role that modeling had in the development process. The paper will also concern the description of relevant applications of these systems.

Type of Paper: Article
Complete Toluene Oxidation on Pt/CeO2-ZrO2-ZnO Catalysts
Min Yeong Kim, Tomoya Kamata, Toshiyuki Masui and Nobuhito Imanaka
Department of Applied Chemistry, Faculty of Engineering, Osaka University, 2-1 Yamadaoka, Suita, Osaka 565-0871, Japan; E-Mail: imanaka@chem.eng.osaka-u.ac.jp
Volatile organic compounds (VOCs) are organic chemical compounds such as aldehydes, ketones, and other light weight hydrocarbons. Since they have relatively high vapor pressures under ambient conditions, they vaporize easily and diffuse into the atmosphere. Some VOCs are harmful to human health and the environment, as recognized to cause sick building syndrome, multiple chemical sensitivity, and air pollution such as photo-chemical smog and ground-level ozone. Among the VOCs, toluene is widely used as an organic solvent for paints, printing inks, adhesives, and antiseptics due to its excellent ability to dissolve organic substances. However, toluene has an unpleasant odor and causes sick building syndrome by evaporating into the atmosphere. To protect our health and the environment from such noxious influences, it is necessary to remove toluene released into the atmosphere as much as possible. In our previous studies, we found that employing solid solutions, which have high oxygen release and storage properties, as promoters was effective to establish complete oxidation of VOCs at moderate temperatures. In particular, introduction of a small amount of SnO2, which has been well-known as a typical n-type semiconductor with electronic conduction, into the CeO2-ZrO2 lattice considerably facilitated the VOCs oxidation. However, thermal stability of the toluene oxidation catalysis on the Pt/CeO2-ZrO2-SnO2 catalysts was not enough due to readily-reducibility of SnO2.In this study, we focused on zinc oxide (ZnO), also known as a stable n-type semiconductor, and a 0.4wt%Pt/Ce0.76Zr0.19Zn0.05O1.95 catalyst was prepared. The catalytic toluene oxidation activity of this catalyst was investigated and calcination temperature dependence on the toluene oxidation activity was characterized. It was confirmed that only CO2 and steam were produced by the complete oxidation of toluene, and no toluene-derived compounds were detected as by-products with a gas chromatography mass spectrometer. Toluene was completely oxidized at 320 °C on the 0.4wt%Pt/Ce0.76Zr0.19Zn0.05O1.95 catalyst calcined at 500 °C. The toluene oxidation activity slightly decreased with increasing the calcination temperature of the catalyst. However, significant deactivation was not recognized in the present 0.4wt%Pt/Ce0.76Zr0.19Zn0.05O1.95 catalyst, and toluene was completely oxidized at 360 °C even after calcination at 1000 °C. From these results, it became obvious that the 0.4 wt%Pt/Ce0.76Zr0.19Zn0.05O1.95 catalyst has high thermal stability for toluene oxidation activity.

Type of Paper: Article
Title: Rh-based Pyrochlore Catalyst for Reforming of Diesel Fuel for Fuel Cell Applications
Authors: James J. Spivey 1 and Dushyant Shekhawat 2
Affiliations: 1 Cain Department of Chemical Engineering, Louisiana State University, S. Stadium Dr., Baton Rouge, LA 70803, USA; E-Mail: jjspivey@lsu.edu
2 U.S. Department of Energy, National Energy Technology Laboratory, 3610 Collins Ferry Road, Morgantown, WV 26507, USA; E-Mail: Dushyant.Shekhawat@NETL.DOE.GOV
Abstract: This paper will be discussing a Rh-based pyrochlore catalyst used for diesel reforming for fuel cell application. The paper will include pre- and post-reaction characterization of the catalyst. Also, it will report results from a 1 000-hr diesel reforming test on a powder pyrochlore catalyst developed by NETL over an oxygen-conducting support demonstrates that the catalyst and support compositions selected have significant potential in a commercial reforming application. Complete hydrocarbon conversion and near equilibrium syngas yields with no signs of catalyst deactivation (olefin formation, pressure buildup, etc.) were observed during reforming of diesel fuel over pyrochlore-based catalyst.

Last update: 20 December 2012

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