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Yongdong Chen

Bio: Yongdong Chen is an academic researcher from Southwest Petroleum University. The author has contributed to research in topics: Catalysis & Hydrogen production. The author has an hindex of 2, co-authored 2 publications receiving 196 citations.

Papers
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Journal ArticleDOI
TL;DR: A detailed analysis based on the spectroscopic technique revealed that reaction pathways proceeded along a mono-functional or bi-functional mechanism according to the types of active metal and support as mentioned in this paper.
Abstract: Hydrogen production from ethanol is regarded as a promising way for energy sustainable development, which is undergoing an explosive growth over the last decade. Besides operating conditions, hydrogen yield greatly dependent on the nature of metal and the support selected. To date, Rh based catalysts proved to be the most active systems due to the fact that Rh possessed the greatest capacity toward C–C bond cleavage. Support also played a critical role in terms of hydrogen selectivity and stability. MgO, CeO2 and La2O3 etc were evidenced as suitable supports because of their basic characteristic and/or redox capacity. A detailed analysis based on the spectroscopic technique revealed that reaction pathways proceeded along a mono-functional or bi-functional mechanism according to the types of active metal and support. Ethanol dehydrogenation and/or dehydration reaction mainly occurred on the support, and the diffusion/transformation of the intermediates took place at the metal–support interface. Meanwhile, active metal accelerated the decomposition reaction. The observed catalyst deactivation was normally assigned to the coke formation, active metal sintering and/or oxidation as well as the impurity in crude bio-ethanol. Hence, the scope of this review is to address the present progress in ethanol reforming for hydrogen production including catalyst development and the analysis of the reaction mechanism and kinetics in order to shed light on the design of high efficient catalyst systems and the fundamental understanding of ethanol conversion at the molecular level.

230 citations

Journal ArticleDOI
01 Nov 2015-Fuel
TL;DR: The influence of calcination temperature on the structural property and catalytic behavior of Ir/CeO2 for oxidative steam reforming of ethanol (OSR) was extensively investigated in this paper.

17 citations


Cited by
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TL;DR: In this paper, an overview of the current best performing catalysts for the reforming and partial oxidizing of liquid hydrocarbons for hydrogen production is summarized, along with a review of the recent progress in these areas of research.
Abstract: One of the most attractive routes for the production of hydrogen or syngas for use in fuel cell applications is the reforming and partial oxidation of hydrocarbons. The use of hydrocarbons in high temperature fuel cells is achieved through either external or internal reforming. Reforming and partial oxidation catalysis to convert hydrocarbons to hydrogen rich syngas plays an important role in fuel processing technology. The current research in the area of reforming and partial oxidation of methane, methanol and ethanol includes catalysts for reforming and oxidation, methods of catalyst synthesis, and the effective utilization of fuel for both external and internal reforming processes. In this paper the recent progress in these areas of research is reviewed along with the reforming of liquid hydrocarbons, from this an overview of the current best performing catalysts for the reforming and partial oxidizing of hydrocarbons for hydrogen production is summarized.

276 citations

Journal ArticleDOI
TL;DR: In this article, a review deals with the currently existing alternatives at the catalyst and reactor level to cope with catalyst deactivation and increase process stability, and then delves with the fundamental phenomena occurring during this catalysts deactivation.
Abstract: Undoubtedly, hydrogen (H2) is a clean feedstock and energy carrier whose sustainable production should be anticipated. The pyrolysis of biomass or waste plastics and the subsequent reforming over base (transition) or noble metals supported catalysts allows reaching elevated H2 yields. However, the catalyst used in the reforming step undergoes a rapid and severe deactivation by means of a series of physicochemical phenomena, including metal sintering, metallic phase oxidation, thermal degradation of the support and, more notoriously, coke deposition. This review deals with the currently existing alternatives at the catalyst and reactor level to cope with catalyst deactivation and increase process stability, and then delves with the fundamental phenomena occurring during this catalyst deactivation. An emphasis is placed on coke deposition and its influence on deactivation, which depends on its location, chemical nature, morphology, precursors or formation mechanism, among others. We also discuss the challenges for increasing the value of the carbon materials formed and therefore, enhance process viability.

248 citations

Journal ArticleDOI
TL;DR: In insights into the intrinsic mechanism involved in catalytic reforming are presented and guidance is provided to the development of novel catalysts and processes for the efficient utilization of oxygenates for energy and environmental purposes.
Abstract: This Review describes recent advances in the design, synthesis, reactivity, selectivity, structural, and electronic properties of the catalysts for reforming of a variety of oxygenates (e.g., from simple monoalcohols to higher polyols, then to sugars, phenols, and finally complicated mixtures like bio-oil). A comprehensive exploration of the structure–activity relationship in catalytic reforming of oxygenates is carried out, assisted by state-of-the-art characterization techniques and computational tools. Critical emphasis has been given on the mechanisms of these heterogeneous-catalyzed reactions and especially on the nature of the active catalytic sites and reaction pathways. Similarities and differences (reaction mechanisms, design and synthesis of catalysts, as well as catalytic systems) in the reforming process of these oxygenates will also be discussed. A critical overview is then provided regarding the challenges and opportunities for research in this area with a focus on the roles that systems of ...

237 citations

Journal ArticleDOI
TL;DR: The theoretical basis behind carbon and sulfur poisoning is studied, before examining the strategies toward carbon and sulphur tolerance used so far in the SOFC literature, and the more extensive relevant heterogeneous catalysis literature is studied for strategies and materials which could be incorporated intocarbon and sulfur tolerant fuel cells.
Abstract: Solid oxide fuel cells (SOFCs) are a rapidly emerging energy technology for a low carbon world, providing high efficiency, potential to use carbonaceous fuels, and compatibility with carbon capture and storage. However, current state-of-the-art materials have low tolerance to sulfur, a common contaminant of many fuels, and are vulnerable to deactivation due to carbon deposition when using carbon-containing compounds. In this review, we first study the theoretical basis behind carbon and sulfur poisoning, before examining the strategies toward carbon and sulfur tolerance used so far in the SOFC literature. We then study the more extensive relevant heterogeneous catalysis literature for strategies and materials which could be incorporated into carbon and sulfur tolerant fuel cells.

220 citations

Journal ArticleDOI
TL;DR: Magnesium hydroxide and magnesium oxide are compounds with favorable and unique properties, leading to a broad range of opportunities for their use in science, and above all in practical applications.

206 citations