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All Journal Bulletin of Chemical Reaction Engineering & Catalysis Bulletin of Chemical Reaction Engineering & Catalysis
Bunjerd Jongsomjit
Department of Chemical Engineering, Chulalongkorn University, Bangkok
Chemical Engineering, Chemistry & Bioengineering Chemistry

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Production of Acetaldehyde via Oxidative Dehydrogenation of Ethanol over AgLi/SiO2 Catalysts Narawich Mukda; Chaowat Autthanit; Piyasan Praserthdam; Bunjerd Jongsomjit
Bulletin of Chemical Reaction Engineering & Catalysis 2020: BCREC Volume 15 Issue 3 Year 2020 (December 2020)
Publisher : Department of Chemical Engineering - Diponegoro University

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.15.3.8702.714-725

Abstract

Three AgLi/SiO2 catalysts containing different types of silica supports [small particle size (SPS), medium particle size (MPS) and large particle size (LPS)] were prepared by incipient wetness co-impregnation techniques and tested in oxidative dehydrogenation of ethanol into acetaldehyde. The catalysts were characterized and evaluated by various characterization techniques (e.g. XRD, N2 physisorption, SEM-EDX, UV-Visible spectroscopy, H2-TPR, and CO2-TPD). This study reveals that the catalyst with the best performance is AgLi/SiO2-LPS with a yield in acetaldehyde of 76.8% at 300 °C. The results obtained with the tested catalysts are discussed, and the reasons of performance improvement caused by the presence of the dispersion of active components, the interaction between active components and silica supports, the textural properties of catalysts and reducibility, are raised. Besides, the cooperation of redox properties (Agnδ+  cluster and Ag0) and weak basic density played a pivotal role in promoting the formation of acetaldehyde from ethanol oxidative dehydrogenation. Copyright © 2021 by Authors, Published by BCREC Group. This is an open access article under the CC BY-SA License (https://creativecommons.org/licenses/by-sa/4.0). 
Impact of AlCl3 and FeCl2 Addition on Catalytic Behaviors of TiCl4/MgCl2/THF Catalysts for Ethylene Polymerization and Ethylene/1-Hexene Copolymerization Thanyathorn Niyomthai; Bunjerd Jongsomjit; Piyasan Praserthdam
Bulletin of Chemical Reaction Engineering & Catalysis 2018: BCREC Volume 13 Issue 3 Year 2018 (December 2018)
Publisher : Department of Chemical Engineering - Diponegoro University

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (651.612 KB) | DOI: 10.9767/bcrec.13.3.2116.393-404

Abstract

The present research focuses on elucidating of the impact of Lewis acids including AlCl3 and FeCl2 addition on catalytic behaviors during ethylene polymerization and ethylene/1-hexene copolymerization over the TiCl4/MgCl2/THF catalyst (Cat. A). In this study, the Cat. A with the absence and presence of Lewis acids was synthesized via the chemical route. Then, all catalyst samples were characterized and tested in the slurry polymerization. For ethylene polymerization, using the Cat. A with the presence of AlCl3 apparently gave the highest activity among other catalysts. In addition, the activity of catalysts tended to increase with the presence of the Lewis acids. This can be attributed to an enhancement of active center distribution by the addition of Lewis acids leading to larger amounts of the isolated Ti species. Moreover, with the presence of Lewis acids, the effect of hydrogen on the decreased activity was also less pronounced. Considering ethylene/1-hexene copolymerization, it revealed that the catalyst with the presence of mixed Lewis acids (AlCl3 + FeCl2) exhibited the highest activity. It is suggested that the presence of mixed Lewis acids possibly caused a change in acidity of active sites, which is suitable for copolymerization. However, activities of all catalysts in ethylene/1-hexene copolymerization were lower than those in ethylene polymerization. The effect of hydrogen on the decreased activity for both polymerization and copolymerization system was found to be similar with the presence of Lewis acids. Based on this study, it is quite promising to enhance the catalytic activity by addition of proper Lewis acids, especially when the pressure of hydrogen increases. The characteristics of polymers obtained upon the presence of Lewis acids will be discussed further in more detail.  
Production of Acetaldehyde via Oxidative Dehydrogenation of Ethanol over AgLi/SiO2 Catalysts Narawich Mukda; Chaowat Autthanit; Piyasan Praserthdam; Bunjerd Jongsomjit
Bulletin of Chemical Reaction Engineering & Catalysis 2020: BCREC Volume 15 Issue 3 Year 2020 (December 2020)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.15.3.8702.714-725

Abstract

Three AgLi/SiO2 catalysts containing different types of silica supports [small particle size (SPS), medium particle size (MPS) and large particle size (LPS)] were prepared by incipient wetness co-impregnation techniques and tested in oxidative dehydrogenation of ethanol into acetaldehyde. The catalysts were characterized and evaluated by various characterization techniques (e.g. XRD, N2 physisorption, SEM-EDX, UV-Visible spectroscopy, H2-TPR, and CO2-TPD). This study reveals that the catalyst with the best performance is AgLi/SiO2-LPS with a yield in acetaldehyde of 76.8% at 300 °C. The results obtained with the tested catalysts are discussed, and the reasons of performance improvement caused by the presence of the dispersion of active components, the interaction between active components and silica supports, the textural properties of catalysts and reducibility, are raised. Besides, the cooperation of redox properties (Agnδ+  cluster and Ag0) and weak basic density played a pivotal role in promoting the formation of acetaldehyde from ethanol oxidative dehydrogenation. Copyright © 2021 by Authors, Published by BCREC Group. This is an open access article under the CC BY-SA License (https://creativecommons.org/licenses/by-sa/4.0). 
Co-Authors Chaowat Autthanit Narawich Mukda Piyasan Praserthdam Thanyathorn Niyomthai