Academic literature on the topic 'Catalytic co-conversion'

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Journal articles on the topic "Catalytic co-conversion"

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Teh, Lee Peng, Sugeng Triwahyono, Aishah Abdul Jalil, Herma Dina Setiabudi, and Muhammad Arif Abdul Aziz. "Catalytic CO Methanation over Mesoporous ZSM5 with Different Metal Promoters." Bulletin of Chemical Reaction Engineering & Catalysis 14, no. 1 (2019): 228. http://dx.doi.org/10.9767/bcrec.14.1.3618.228-237.

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The carbon monoxide methanation has possessed huge potential as an effective method to produce synthetic natural gas (SNG). The basic requirements such as high catalytic activity at low temperatures (<500 °C) and high stability throughout all temperatures is needed for an ideal methanation catalysts. The ultimate goal of the study is to examine the influential of different metal promoters towards catalytic properties and catalytic CO methanation performance. A series of metal promoters (Rh, Co, Pd and Zn) mesoporous ZSM5 were synthesized using an incipient-wetness impregnation method and ev
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ASTANOVSKY, D., L. ASTANOVSKY, B. RAIKOV, and N. KORCHAKA. "Reactor for steam catalytic hydrocarbon conversion and catalytic CO conversion in hydrogen production." International Journal of Hydrogen Energy 19, no. 8 (1994): 677–81. http://dx.doi.org/10.1016/0360-3199(94)90153-8.

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Niu, Xiaowei, Liang Zhou, Xiaojun Hu, and Wei Han. "Mesoporous CexCo1−xCr2O4 spinels: synthesis, characterization and catalytic application in simultaneous removal of soot particulate and NO." RSC Advances 5, no. 65 (2015): 52595–601. http://dx.doi.org/10.1039/c5ra04759e.

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Zhao, Pengfei, Pengfei Yu, Zijian Feng, et al. "A mullite oxide catalyst of SmMn2O5 for three-way catalysis: synthesis, characterization, and catalytic activity evaluation." RSC Advances 6, no. 70 (2016): 65950–59. http://dx.doi.org/10.1039/c6ra12313a.

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Hu, Yun Hang. "(Invited) Catalytical Conversion of CO2 into Chemicals and Fuels: From Thermal Catalysis to Thermo-Photo Hybrid Catalysis." ECS Meeting Abstracts MA2025-01, no. 39 (2025): 2062. https://doi.org/10.1149/ma2025-01392062mtgabs.

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CO2 is the most significant greenhouse gas, and its catalytic conversion into value-added chemicals and fuels represents the most efficient strategy for its utilization. Thermal catalytic processes typically achieve high CO2 conversion but exhibit low selectivity. In contrast, photocatalytic processes often offer high selectivity but generally result in low CO₂ conversion. To solve this issue, we developed a thermo-photo hybrid catalytic approach for CO2 conversion. This presentation will cover the design and development of efficient catalysts for the thermal catalytic reforming of CO2 and sho
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Zhou, Xin-Yan, Bo Fu, Wen-Dong Jin, et al. "Efficient and Selective Oxygenation of Cycloalkanes and Alkyl Aromatics with Oxygen through Synergistic Catalysis of Bimetallic Active Centers in Two-Dimensional Metal-Organic Frameworks Based on Metalloporphyrins." Biomimetics 8, no. 3 (2023): 325. http://dx.doi.org/10.3390/biomimetics8030325.

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Confined catalytic realms and synergistic catalysis sites were constructed using bimetallic active centers in two-dimensional metal-organic frameworks (MOFs) to achieve highly selective oxygenation of cycloalkanes and alkyl aromatics with oxygen towards partly oxygenated products. Every necessary characterization was carried out for all the two-dimensional MOFs. The selective oxygenation of cycloalkanes and alkyl aromatics with oxygen was accomplished with exceptional catalytic performance using two-dimensional MOF Co-TCPPNi as a catalyst. Employing Co-TCPPNi as a catalyst, both the conversion
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Xu, Tao, Xiuren Zheng, Jue Xu, and Yongping Wu. "Hydrogen-Rich Gas Production from Two-Stage Catalytic Pyrolysis of Pine Sawdust with Nano-NiO/Al2O3 Catalyst." Catalysts 12, no. 3 (2022): 256. http://dx.doi.org/10.3390/catal12030256.

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Hydrogen production from biomass pyrolysis is economically and technologically attractive from the perspectives of energy and the environment. The two-stage catalytic pyrolysis of pine sawdust for hydrogen-rich gas production is investigated using nano-NiO/Al2O3 as the catalyst at high temperatures. The influences of residence time (0–30 s) and catalytic temperature (500–800 °C) on pyrolysis performance are examined in the distribution of pyrolysis products, gas composition, and gas properties. The results show that increasing the residence time decreased the solid and liquid products but incr
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Vjunov, Aleksei, Karl C. Kharas, Vasileios Komvokis, Amy Dundee, Claire C. Zhang, and Bilge Yilmaz. "Pragmatic Approach toward Catalytic CO Emission Mitigation in Fluid Catalytic Cracking (FCC) Units." Catalysts 11, no. 6 (2021): 707. http://dx.doi.org/10.3390/catal11060707.

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The need to mitigate the environmental footprints of refineries in a sustainable and economical way is widely accepted, yet there appears to be a lack of a unilateral pragmatic approach towards CO oxidation to CO2 among the refining community. In this work we share CO promoter design strategies that can afford a tangible and immediate CO conversion efficiency increase without a need for additional precious metal loading. The key focus is on the support material architecture that is essential to boost the CO conversion and reduce the NOx generation in the FCC unit. It was demonstrated that the
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Gao, Yan, Wenchao Jiang, Tao Luan, et al. "High-Efficiency Catalytic Conversion of NOx by the Synergy of Nanocatalyst and Plasma: Effect of Mn-Based Bimetallic Active Species." Catalysts 9, no. 1 (2019): 103. http://dx.doi.org/10.3390/catal9010103.

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Three typical Mn-based bimetallic nanocatalysts of Mn−Fe/TiO2, Mn−Co/TiO2, Mn−Ce/TiO2 were synthesized via the hydrothermal method to reveal the synergistic effects of dielectric barrier discharge (DBD) plasma and bimetallic nanocatalysts on NOx catalytic conversion. The plasma-catalyst hybrid catalysis was investigated compared with the catalytic effects of plasma alone and nanocatalyst alone. During the catalytic process of catalyst alone, the catalytic activities of all tested catalysts were lower than 20% at ambient temperature. While in the plasma-catalyst hybrid catalytic process, NOx co
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Al Soubaihi, Rola Mohammad, Khaled Mohammad Saoud, Myo Tay Zar Myint, Mats A. Göthelid, and Joydeep Dutta. "CO Oxidation Efficiency and Hysteresis Behavior over Mesoporous Pd/SiO2 Catalyst." Catalysts 11, no. 1 (2021): 131. http://dx.doi.org/10.3390/catal11010131.

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Carbon monoxide (CO) oxidation is considered an important reaction in heterogeneous industrial catalysis and has been extensively studied. Pd supported on SiO2 aerogel catalysts exhibit good catalytic activity toward this reaction owing to their CO bond activation capability and thermal stability. Pd/SiO2 catalysts were investigated using carbon monoxide (CO) oxidation as a model reaction. The catalyst becomes active, and the conversion increases after the temperature reaches the ignition temperature (Tig). A normal hysteresis in carbon monoxide (CO) oxidation has been observed, where the cata
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Dissertations / Theses on the topic "Catalytic co-conversion"

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Chafik, Abdelghani. "Influence de terres rares (La, Ce) sur les propriétés de systèmes catalytiques Métal-Carbone (Métal : Fe, Co, Ni) dans la conversion d'oxydes de carbone." Poitiers, 1988. http://www.theses.fr/1988POIT2309.

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Almuqati, Naif. "Preparation of bulk and supported Co/Mo carbide catalysts for CO2 conversion." Thesis, University of Oxford, 2013. http://ora.ox.ac.uk/objects/uuid:85227298-930c-428c-b975-6097f3e5b6a2.

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This thesis investigates the preparation and characterisation of Co/Mo bimetallic carbides and their stability and catalytic activity as bulk catalysts for the Dry Methane Reforming (DMR) reaction and as supported catalysts on alumina. The DMR reaction was chosen due to its importance in producing syngas, as a precursor for liquid fuels, from CO<sub>2</sub> and CH<sub>4</sub>, two greenhouse gases. Bulk and supported bimetallic carbides were prepared by reductive carburization of the oxides with various hydrocarbons. The resultant carbides were characterized by X-Ray diffraction. Reactivity st
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Ponsard, Louise. "Conversion catalytique du CO pour la synthèse de monomères oxygénés." Thesis, université Paris-Saclay, 2021. http://www.theses.fr/2021UPASF002.

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Les produits de l’industrie chimique sont aujourd’hui principalement issus de ressources fossiles non renouvelables. Leur exploitation entraine l’émission de gaz à effet de serre, ayant pour conséquence directe une crise climatique sans précédent. Les petites molécules carbonées (CO et CO₂), aujourd’hui considérées comme des déchets, apparaissent comme des sources attractives de carbone pour assurer la transition de notre économie vers une économie circulaire. Le CO est une petite molécule réactive émise comme déchet par l’industrie chimique, ou pouvant être produite par réduction de CO₂. Une
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Hare, Bryan J. "Supported Perovskite-type Oxides: Establishing a Foundation for CO2 Conversion through Reverse Water-gas Shift Chemical Looping." Scholar Commons, 2018. https://scholarcommons.usf.edu/etd/7628.

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Perovskite-type oxides show irrefutable potential for feasible thermochemical solar-driven CO2 conversion. These materials exhibit the exact characteristics required by the low temperature reverse water-gas shift chemical looping process. These properties include structural endurance and high oxygen redox capacity, which results in the formation of numerous oxygen vacancies, or active sites for CO2 conversion. A major drawback is the decrease in oxygen self-diffusion with increasing perovskite particle size. In this study, the La0.75Sr0.25FeO3 (LSF) perovskite oxide was combined with various s
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Jiménez-Calvo, Pablo Isaí. "Synthèses, caractérisations et performances de matériaux à base de g-C3N4 décorés avec des nanoparticules d´Au pour des applications (photo) catalytiques." Thesis, Strasbourg, 2019. http://www.theses.fr/2019STRAF012/document.

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À ce jour, l’humanité est confrontée simultanément à une crise énergétique et environnementale due principalement à deux facteurs: la croissance démographique et la dépendance aux combustibles fossiles. C'est pourquoi l'urgence d'utiliser des sources d'énergie renouvelables, comme l'énergie solaire est une, solution potentielle. A ce titre, la production d'H2 décarboné par dissociation solaire de l'eau est une voie prometteuse. Néanmoins, pour atteindre l'objectif mentionné, il faut trouver un système photocatalytique (semi-conducteurs, SCs) idéal, qui nécessite quatre caractéristiques majeure
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Thegarid, Nicolas. "Synthèse d’essences hybrides par co-traitement de distillats de pétrole et d’huiles de pyrolyse de bio-masse en craquage catalytique." Thesis, Lyon 1, 2013. http://www.theses.fr/2013LYO10034.

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La pyrolyse de la biomasse ligno-cellulosique permet la production de bio-huiles dans la perspective à court terme de carburants hybrides contenant une fraction de bio-carbone dans un carburant conventionnel d'origine fossile (essence ou diesel). Cependant, la forte concentration en oxygène dans ces huiles, leur instabilité et faible densité énergétique (comparée aux carburants fossiles) imposent des pré-traitements permettant cette co-synthèse de carburants hybrides. Ainsi, après hydrotraitement ou ajout d’un catalyseur durant la pyrolyse, ces bio-huiles peuvent être mélangées à un distillat
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Corda, Massimo. "Catalyst Design and Mechanistic Insights into COx Hydrogenation to Methanol and Light Olefins." Electronic Thesis or Diss., Université de Lille (2022-....), 2024. https://pepite-depot.univ-lille.fr/ToutIDP/EDSMRE/2024/2024ULILR037.pdf.

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L'augmentation de la concentration de CO2 atmosphérique présente des défis environnementaux significatifs et souligne l'urgence de développer des procédés chimiques durables. Une approche prometteuse pour aborder ces problèmes est la conversion catalytique du CO2 en produits chimiques à valeur ajoutée, tels que le méthanol et les oléfines légères. Cette thèse se concentre sur le développement de catalyseurs pour la synthèse de méthanol et la synthèse d'oléfines légères à partir de CO2 par médiation de méthanol. De plus, l'hydrogénation du CO médiée par le méthanol en oléfines légères est égale
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Padayachee, Diandree. "Manganese oxide- based gold catalysts for low temperature CO conversion." Thesis, 2015. http://hdl.handle.net/10539/18804.

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Thesis ( M.Sc)--University of the Witwatersrand, Faculty of Science, 2003<br>Initial investigations at Mintek, into the addition of gold to commercial hopcalite (CuxMnyOz), showed that it improved the activity of hopcalite. So this study was initially focused on investigating Aulhopcalite catalysts further. Also, since according to literature, MnxOy has catalytic potential, the study of AulMnxOy catalysts was included. Au/hopcalite and Aul/nxOy catalysts were made by means of deposition-precipitation, colloidal gold deposition and co-precipitation. Only one catalyst-type was highly acti
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Book chapters on the topic "Catalytic co-conversion"

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Schlögl, Robert. "Chemical-Catalytic Conversion of CO2 and CO." In CO2 and CO as Feedstock. Springer International Publishing, 2023. http://dx.doi.org/10.1007/978-3-031-27811-2_6.

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Bhattacharyya, Sohini, Soumyabrata Roy, and P. M. Ajayan. "An Overview of Catalytic CO2 Conversion." In ACS Symposium Series. American Chemical Society, 2022. http://dx.doi.org/10.1021/bk-2022-1412.ch009.

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Adjaye, John D., Ramesh K. Sharma, and Narendra N. Bakhshi. "Catalytic Upgrading of Wood Derived Bio-Oil over HZSM-5 Catalyst: Effect of Co-Feeding Steam." In Advances in Thermochemical Biomass Conversion. Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-1336-6_79.

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Anadebe, Valentine Chikaodili, Abhinay Thakur, Chukwunonso Chukwuzuluoke Okoye, Ifechukwu Godfrey Ezemagu, Lei Guo, and Eno E. Ebenso. "Carbon Dots in Catalysis: CO2 Conversion, H2 Evolution, and Organic Reactions." In ACS Symposium Series. American Chemical Society, 2024. http://dx.doi.org/10.1021/bk-2024-1465.ch013.

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van Leeuwen, Piet W. N. M. "Organometallic Chemistry and Elementary Steps." In Contemporary Catalysis: Science, Technology, and Applications. The Royal Society of Chemistry, 2017. http://dx.doi.org/10.1039/9781849739900-00087.

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The entire science of chemistry can be thought of as the underlying knowledge of catalysis, since each conversion can be subjected to catalysis, each material might function as a catalyst, each spectroscopic technique may prove useful one day in catalysis, and catalytic processes are amongst the most intriguing theoretical targets. Yet, in only a small number of pages, we will outline here what we think are the key underlying principles for catalysis. The organometallic chemistry we discuss in this chapter deals with the most often used concepts of chemical bonding related to catalysis and the
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Lambert, Tristan H. "Functional Group Reduction." In Organic Synthesis. Oxford University Press, 2015. http://dx.doi.org/10.1093/oso/9780190200794.003.0010.

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The reduction of azobenzene 1 with catalyst 2 was reported (J. Am. Chem. Soc. 2012, 134, 11330) by Alexander T. Radosevich at Pennsylvania State University, representing a unique example of a nontransition metal-based two-electron redox catalysis platform. Wolfgang Kroutil at the University of Graz found (Angew. Chem. Int. Ed. 2012, 51, 6713) that diketone 4 was converted to piperidinium 5 with very high stereoselectivity using a transaminase followed by reduction over Pd/C. Dennis P. Curran at the University of Pittsburgh reported (Org. Lett. 2012, 14, 4540) that NHC-borane 7 is a convenient
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Ansari, Khursheed B., Shakeelur Rahman A. R., Mohd Shariq Khan, Saleem Akhtar Farooqui, Mohd Yusuf Ansari, and Mohammad Danish. "Conversion of Biomass to Green Gasoline: Feedstocks, Technological Advances and Commercial Scope." In Green Gasoline. Royal Society of Chemistry, 2023. http://dx.doi.org/10.1039/bk9781837670079-00124.

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Biomass-driven energy has attracted considerable attention in recent decades as an alternative to petroleum fuel, particularly diesel and gasoline. Green gasoline production through the hydroprocessing of biomass/plant materials is one innovative approach that has brought biorefinery facilities to the forefront. Several biomass-based feedstocks, including wood chips, bagasse, vegetable oils and blends of bio-oil and petroleum oil, are being investigated for green gasoline production. Of these, vegetable oils produce kerosene and diesel-range hydrocarbons (C15–C20) along with gasoline, and the
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Carlucci, Claudia, and Ana Melisa Jiménez-Ramirez. "Biofuel from seeds, extraction oil and its efficiency." In PLANTS: Physiology, crop production, and stress responses. Editora Científica Digital, 2025. https://doi.org/10.37885/250419151.

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The increasing global demand for renewable energy has stimulated extensive research into biodiesel production from vegetable oils via continuous flow methodologies, due to their superior efficiency, safety, and scalability compared to conventional batch processes. This study explores the synthesis of biodiesel from various oil sources—such as palm, soybean, jatropha, canola, sunflower, rapeseed, and cottonseed—employing a wide range of reactors including microtube, bubble column, fixed-bed, membrane, slit-channel, vortex, and reactive distillation systems. The research aimed to compare the con
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Pan, Ying, Antara Bhowmick, Lu Liu, Chen Zhang, and Dongxia Liu. "Non-oxidative propane dehydrogenation in membrane reactors." In Catalysis. Royal Society of Chemistry, 2024. http://dx.doi.org/10.1039/bk9781837672035-00135.

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Propylene (C3H6) is a building block for important petrochemicals production such as polypropylene and acrylonitrile. Propylene is traditionally produced as a co-product in steam crackers (SC) and as a by-product in fluid catalytic cracking (FCC) units. A growing gap between the supply and demand for C3H6 is expected in the foreseeable future. On-purpose C3H6 production, such as non-oxidative propane dehydrogenation (PDH), is considered as a suitable technology to bridge the gap between conventional processes (SC and FCC) and the demand for C3H6. However, the PDH process faces challenges due t
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Pala-Rosas, Israel, José L. Contreras, José Salmones, Ricardo López-Medina, Beatriz Zeifert, and Naomi N. González Hernández. "Sustainable Synthesis of Pyridine Bases from Glycerol." In Ethanol Chemistry - Production, Modelling, Applications, and Technological Aspects [Working Title]. IntechOpen, 2023. http://dx.doi.org/10.5772/intechopen.111939.

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Catalytic processes have been developed to obtain pyridine bases from glycerol, either by direct conversion or with acrolein as an intermediate. When producing acrolein as an intermediate, the reaction may proceed in a single reactor at temperatures above 400°C in co-feeding with ammonia. A system of two interconnected reactors can also be used: one reactor performs the catalytic dehydration of glycerol to acrolein, while in the second reactor acrolein reacts with ammonia to form pyridine bases. Both processes require the use of solid acid catalysts, for which ZSM-5 zeolite-based catalysts are
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Conference papers on the topic "Catalytic co-conversion"

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Li, Haoyang, Xue Han, Kaiyang Li, Minkang Liu, Yimin Zeng, and Chunbao (Charles) Xu. "Corrosion of UNS N06625 under Batch-Mode Biomass Supercritical Water Gasification (SCWG) of Lignin." In CONFERENCE 2022. AMPP, 2022. https://doi.org/10.5006/c2022-18030.

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Abstract Supercritical water gasification (SCWG) is a thermochemical conversion technology developed to transform various feedstocks, such as raw forest biomass materials, crude bio-oils and bio-wastes, into syngas (a combination of CO and H2) for clean energy production. Despite the intensive research efforts that have been applied on the development of SCWG technology, the optimal SCWG operating parameters (temperature, pressure, and biomass/water ratio, etc.) are not well defined because of the complexity of feedstock types and conversion reactor configurations (batch or continuous mode). M
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Abo-Ghander, Nabeel S., and Filip Logist. "Optimal Hydrogen Flux in a Catalytic Membrane Water Gas Shift Reactor." In The 35th European Symposium on Computer Aided Process Engineering. PSE Press, 2025. https://doi.org/10.69997/sct.106375.

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A one-dimensional homogeneous reactor model for a cocurrent flow nonadiabatic catalytic membrane reactor operating water gas shift reaction (WGSR) is developed. The model is used to predict the performance of the reactor and estimate the optimal hydrogen flux profiles required to maximize the CO conversion, and control the temperature rise due to the exothermicity. Under the optimized condition, the secured optimal hydrogen flux is found to be a bang-bang type suggesting constructing reactors of different hydrogen permeabilities. To control the reactor temperature, the activity of the reaction
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Markova, Mariia, Antonina Stepacheva, Vladimir Molchanov, Galina Demidenko, and Mikhail Sulman. "FISCHER-TROPSCH SYNTHESIS OVER POLYMER SUPPORTED PROMOTED IRON CATALYSTS." In 24th SGEM International Multidisciplinary Scientific GeoConference 24. STEF92 Technology, 2024. https://doi.org/10.5593/sgem2024/4.1/s17.12.

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In recent decades, the interest of researchers has focused on the development of methods for obtaining alternative energy sources. Fischer-Tropsch synthesis is one of the methods for obtaining a wide range of hydrocarbons and their derivatives. Ru, Ni, Fe and Co are the widely used catalytically active metals in FTS. To increase the activity of the catalyst, as well as increase the yield of target products, promoters are introduced into catalytic systems. In FTS, oxides of alkaline and rare earth metals, oxides of lanthanides and actinides, and noble metals are used as modifiers. In this work,
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Kong, D., X. Chen, and W. Xia. "Research on the synergistic catalytic conversion of CO2 using a gliding arc plasma coupled with a fluidized bed." In 2024 IEEE International Conference on Plasma Science (ICOPS). IEEE, 2024. http://dx.doi.org/10.1109/icops58192.2024.10626500.

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Pappagallo, M. Andrea, Tilman J. Schildhauer, Oliver Kr�cher, and Emanuele Moioli. "A New Method to Assess Performance Loss due to Catalyst Deactivation in Fixed- and Fluidized-bed Reactors." In The 35th European Symposium on Computer Aided Process Engineering. PSE Press, 2025. https://doi.org/10.69997/sct.136705.

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A new methodology for the assessment of the performance loss in catalytic reactors due to deactivation was developed and applied to fixed- and fluidized-bed CO methanation, with catalyst subject to coking. The methodology is based on the solution of heat and mass balances, by decoupling the reactor and deactivation dynamics. This is possible by using consecutive 1D, steady-state calculations for the characterization of the reactor performance. In this way, the progressively lower values of catalyst activity along the time on stream are computed with the integration of a dedicated dynamic model
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Liu, S., L. Ren, D. Mei, and Z. Fang. "Efficient plasma-catalysis coupling for CH4 and CO2 conversion in a dielectric barrier discharge." In 2024 IEEE International Conference on Plasma Science (ICOPS). IEEE, 2024. http://dx.doi.org/10.1109/icops58192.2024.10627196.

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Shamim, Tariq. "Dynamic Response of Automotive Catalytic Converters to Modulations in Engine Exhaust Compositions." In ASME 2003 Internal Combustion Engine Division Spring Technical Conference. ASMEDC, 2003. http://dx.doi.org/10.1115/ices2003-0669.

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This paper presents a computational investigation of the effect of composition modulations on an automotive catalytic converter. The objective is to develop a better fundamental understanding of the converter’s performance under actual driving conditions. Such an understanding will be beneficial in devising improved emission control methodologies by exploiting the catalyst transient behavior. The study employs a single-channel based, one-dimensional, non-adiabatic model. Two types of imposed transients (sinusoidal and step changes) are considered. The results show that composition modulations
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Hotz, Nico. "Nano-Structured Catalytic Material for Solar-Powered Biofuel Reforming." In ASME 2012 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 2012. http://dx.doi.org/10.1115/imece2012-89729.

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The main goal of this project is to combine two renewable energy conversion technologies (low-temperature fuel cells and solarthermal collectors) to achieve synergies in terms of cost and energetic efficiency compared to systems based on a single energy source and energy conversion technology. Direct solar-to-electric energy conversion, such as photovoltaics, is currently not economically competitive with traditional electric power generation. Fuel cell technology using alcoholic fuel possibly generated from biomass (e.g. methanol) is not competitive in terms of costs either. The system propos
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Struk, P. M., D. L. Dietrich, F. J. Miller, and J. S. T’ien. "Transient Numerical Modeling of Catalytic Channels." In ASME 2007 International Mechanical Engineering Congress and Exposition. ASMEDC, 2007. http://dx.doi.org/10.1115/imece2007-41680.

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This paper presents a transient model of catalytic combustion suitable for isolated channels and monolith reactors. The model is a “lumped” two-phase (gas and solid) model where the gas phase is quasi-steady relative to the transient solid. Axial diffusion is neglected in the gas phase; lateral diffusion, however, is accounted for using transfer coefficients. The solid phase includes axial heat conduction and external heat loss due to convection and radiation. The combustion process utilizes detailed gas and surface reaction models. The gas-phase model becomes a system of stiff ordinary differ
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Chan, S. H., and D. L. Hoang. "Modeling of Catalytic Conversion of CO/HC in Gasoline Exhaust at Engine Cold-Start." In International Congress & Exposition. SAE International, 1999. http://dx.doi.org/10.4271/1999-01-0452.

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Reports on the topic "Catalytic co-conversion"

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Zhou, S., Vasudev Haribal, and Raghubir Gupta. Plasma-Assisted Catalytic Conversion of CO2 and Propane to Propylene and CO. Office of Scientific and Technical Information (OSTI), 2023. http://dx.doi.org/10.2172/2202683.

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Zhou, S. James, and Vasudev Haribal. Plasma Assisted Catalytic Conversion of Carbon Dioxide (CO2) and Propane to Propylene and Carbon Monoxide (CO). Office of Scientific and Technical Information (OSTI), 2021. https://doi.org/10.2172/2564985.

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Zhou, S. James, Vasudec Haribal, Raghubir Gupta, et al. Plasma Assisted Catalytic Conversion of Carbon Dioxide (CO2) and Propane to Propylene and Carbon Monoxide (CO). Office of Scientific and Technical Information (OSTI), 2022. https://doi.org/10.2172/2564986.

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