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Bulletin of Chemical Reaction Engineering & Catalysis
Published by Masyarakat Katalis Indonesia - Indonesian Catalyst Society
ISSN : -     EISSN : 19782993     DOI : https://doi.org/10.9767/bcrec
Core Subject : Science, Engineering,
Chemical Engineering, Chemistry & Bioengineering Chemistry
Bulletin of Chemical Reaction Engineering & Catalysis, a reputable international journal, provides a forum for publishing the novel technologies related to the catalyst, catalysis, chemical reactor, kinetics, and chemical reaction engineering. Scientific articles dealing with the following topics in chemical reaction engineering, catalysis science, and engineering, catalyst preparation method and characterization, novel innovation of chemical reactor, kinetic studies, etc. are particularly welcome. However, articles concerned on the general chemical engineering process are not covered and out of the scope of this journal. This journal encompasses Original Research Articles, Review Articles (only selected/invited authors), and Short Communications, including: fundamentals of catalyst and catalysis; materials and nano-materials for catalyst; chemistry of catalyst and catalysis; surface chemistry of catalyst; applied catalysis; applied bio-catalysis; applied chemical reaction engineering; catalyst regeneration; catalyst deactivation; photocatalyst and photocatalysis; electrocatalysis for fuel cell application; applied bio-reactor; membrane bioreactor; fundamentals of chemical reaction engineering; kinetics studies of chemical reaction engineering; chemical reactor design (not process parameter optimization); enzymatic catalytic reaction (not process parameter optimization); kinetic studies of enzymatic reaction (not process parameter optimization); the industrial practice of catalyst; the industrial practice of chemical reactor engineering; application of plasma technology in catalysis and chemical reactor; and advanced technology for chemical reactors design. However, articles concerned about the "General Chemical Engineering Process" are not covered and out of the scope of this journal.
Arjuna Subject : Teknik Kimia (semua kategori) - Katalisis
Articles 838 Documents
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Catalyst in Basic Oleochemicals Eva Suyenty; Herlina Sentosa; Mariani Agustine; Sandy Anwar; Abun Lie; Erwin Sutanto
Bulletin of Chemical Reaction Engineering & Catalysis 2007: BCREC: Volume 2 Issues 2-3 Year 2007 (October 2007)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.2.2-3.6.22-31

Abstract

Currently Indonesia is the world largest palm oil producer with production volume reaching 16 million tones per annum. The high crude oil and ethylene prices in the last 3 – 4 years contribute to the healthy demand growth for basic oleochemicals: fatty acids and fatty alcohols. Oleochemicals are starting to replace crude oil derived products in various applications. As widely practiced in petrochemical industry, catalyst plays a very important role in the production of basic oleochemicals. Catalytic reactions are abound in the production of oleochemicals: Nickel based catalysts are used in the hydrogenation of unsaturated fatty acids; sodium methylate catalyst in the transesterification of triglycerides; sulfonic based polystyrene resin catalyst in esterification of fatty acids; and copper chromite/copper zinc catalyst in the high pressure hydrogenation of methyl esters or fatty acids to produce fatty alcohols. To maintain long catalyst life, it is crucial to ensure the absence of catalyst poisons and inhibitors in the feed. The preparation methods of nickel and copper chromite catalysts are as follows: precipitation, filtration, drying, and calcinations. Sodium methylate is derived from direct reaction of sodium metal and methanol under inert gas. The sulfonic based polystyrene resin is derived from sulfonation of polystyrene crosslinked with di-vinyl-benzene. © 2007 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)
Catalytic Hydrothermal Liquefaction of Sugarcane Bagasse: Effect of Crystallization Time of Fe-MCM-41 and Process Parameters Gopalakrishnan Govindasamy; Rohit Sharma; Sunu Subramanian
Bulletin of Chemical Reaction Engineering & Catalysis 2022: BCREC Volume 17 Issue 4 Year 2022 (December 2022)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.17.4.15781.768-777

Abstract

Sugarcane is both food and energy crop providing sugar and energy products. Hydrothermal liquefaction (HTL) is gaining importance for the conversion of sugarcane bagasse to bio-oil, whose yield depends on the deoxygenation activity of the catalyst employed and process parameters. In this study, mesoporous Fe-MCM-41 catalysts were synthesized with crystallization time varied from 12 to 72 h, characterized by X-ray Diffraction (XRD), textural analysis, Scanning Electron Microscope (SEM), Energy Dispersive X-ray (EDX), and evaluated for the HTL of sugarcane bagasse. All the Fe-MCM-41 catalysts gave higher bio-oil yield with lower oxygen content compared to non-catalytic HTL, confirmed their deoxygenation activity. Among them, Fe-MCM-41 synthesized after 24 h of crystallization was found to have the highest crystallinity, and surface area thus gave the highest bio-oil yield of 56.2% containing the least amount of oxygen of 15.3 wt% at 250 °C, initial CO pressure of 45 bar, reaction time of 120 min, Water/Biomass weight ratio of 28, Catalyst/Biomass weight ratio of 0.4 and 0.2, respectively. Overall process of HTL of sugarcane bagasse was found to involve two consecutive equilibria, first conversion of lignocellulose of sugarcane bagasse by hydrolysis to water soluble organics (WSO) followed by its deoxygenation to bio-oil. Copyright © 2022 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). 
Oxidation of Catechol using Titanium Silicate (TS-1) Catalyst: Modeling and Optimization Sonali Sengupta; Debarpita Ghosal; Jayanta K. Basu
Bulletin of Chemical Reaction Engineering & Catalysis 2013: BCREC Volume 8 Issue 2 Year 2013 (December 2013)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.8.2.4759.167-177

Abstract

The oxidation of catechol was studied in an eco-friendly process with commercial titanium silicate-1 (TS-1) catalyst and hydrogen peroxide as oxidant in absence of all mass transfer effects. The process was opti-mized by Box-Behnken design in terms of three independent process variables such as reaction tempera-ture, moles of hydrogen peroxide per mole of catechol and catalyst amount whose optimum values of the process variables were found to be 60 °C, 13.2 and 1.24 g respectively for maximum conversion of 75.8 %. The effects of different process parameters such as mole ratio of hydrogen peroxide to catechol, catalyst par-ticle size, catalyst amount, temperature and reaction time were studied. A pseudo first order kinetic model was fitted with the experimental rate data. The apparent activation energy for the reaction was found to be 11.37 kJ/mole. © 2013 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)
Polyoxometalate Intercalated M2+/Al (M2+=Ni, Mg) Layered Double Hydroxide for Degradation of Methylene Blue Yulizah Hanifah; Risfidian Mohadi; Mardiyanto Mardiyanto; Nur Ahmad; Suheryanto Suheryanto; Aldes Lesbani
Bulletin of Chemical Reaction Engineering & Catalysis 2023: BCREC Volume 18 Issue 2 Year 2023 (August 2023)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.17789

Abstract

The synthesis and characterization of M2+/Al (M2+=Ni, Mg) layered double hydroxide (LDH) and intercalated polyoxometalate is presented. We have reported the growth of polyoxometalate on Ni/Mg layered double hydroxide for degradation methylene blue (MB). By considering variables such as pH of dye solution, dye concentration, and time as degradation variables, the efficiency of organic dye degradation and degradation parameters of M2+/Al (M2+ = Ni, Mg) LDH and both composite LDH-polyoxometalate has been identified. X-Ray Diffraction (XRD), Fourier Transform Infra Red (FTIR), Scanning Electron Microscope (SEM), and Ultra Violet Diffuse Reflectance Spectroscopy (UV-DRS) spectroscopy confirmed the layered double hydroxide structure. XRD and FTIR analysis confirmed the single-phase of the as-made and polyoxometalate intercalated LDH. SEM images show the formation of aggregates of small various sizes. The material’s photodegradation was assessed through methylene blue (MB) degradation process. The result showed that NiAl-Si has a good degradation capacity for MB as compared to NiAl-Pw, MgAl-Si, and MgAl-PW. The result shows that LDH composite presents stability and has good photocatalytic activities toward the reduction of methylene blue. The FTIR measurement confirming the LDH composite structure reveals the materials used in the fifth regeneration. The activity of MB photodegradation pristine were NiAl (45%), MgAl (43%), NiAl-Pw (78%), NiAl-Si (85%), MgAl-Pw (58%), and MgAl-Si (75%), respectively. The LDH-polyoxometalate composite material’s capacity to successfully photodegrade, as measured by the percentage of degradation, revealed an increase in photodegradation catalysis and the ability of the LDH to regenerate. Copyright © 2023 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). 
Benzylation of Toluene over Iron Modified Mesoporous Ceria K. J. Rose Philo; Sugunan Sugunan
Bulletin of Chemical Reaction Engineering & Catalysis 2012: BCREC Volume 7 Issue 2 Year 2012 (December 2012)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.7.2.3759.158-164

Abstract

Green chemistry has been looked upon as a sustainable science which accomplishes both economical and environmental goals, simultaneously.With this objective, we developed an alternative process to obtain the industrially important benzyl aromatics by benzylation of aromatics using benzyl chloride, catalysed by mesoporous solid acid catalysts. In this work mesoporous ceria is prepared using neutral surfactant which helped the calcination possible at a lower temperature enabling a higher surface area. Mesoporous ceria modified with Fe can be successfully utilized for the selective benzylation of toluene to more desirable product methyl diphenyl methane with 100% conversion and selectivity in 2 hours using only 50mg of the catalyst under milder condition. The reusability, regenerability, high selectivity, 100% conversion, moderate reaction temperature and absence of solvent, etc. make these catalysts to be used in a truly heterogeneous manner and make the benzylation reaction an environment friendly one. © 2012 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)
Advancements in the Exploration of Gel Electrolytes for Aqueous Zinc Ion Batteries Yi Xiong; Jinhang Dai; Lingyao Kuang; Xiaodan Li; Xingxing Gu
Bulletin of Chemical Reaction Engineering & Catalysis 2023: BCREC Volume 18 Issue 3 Year 2023 (October 2023)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.19816

Abstract

Aqueous zinc-ion batteries (ZIBs) are seen as a superior substitute for lithium-ion batteries (LIBs) due to their excellent safety, low cost, and eco-friendliness. However, problems such as zinc dendrite growth, hydrogen evolution reaction and electrode corrosion hinder the commercialization of batteries. Electrolyte as a link to other parts of the battery, has been widely concerned. Hydrogel is a kind of cross-linked product filled with water, which has the advantages of high theoretical capacity, good flexibility, good water retention and good mechanical properties, and becomes a potential candidate for ZIBs. By summarizing the development of hydrogel electrolytes, the cross-linking types of gel electrolytes and their applications in ZIBs were reviewed in this paper. Finally, the application of gel electrolyte in ZIBs is summarized and prospected, which brings a meaningful reference for the development of ZIBs. Copyright © 2023 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). 
Application of La-ZSM-5 Coated Silicon Carbide Foam Catalyst for Toluene Methylation with Methanol Debarpita Ghosal; Jayanta Kumar Basu; Sonali Sengupta
Bulletin of Chemical Reaction Engineering & Catalysis 2015: BCREC Volume 10 Issue 2 Year 2015 (August 2015)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.10.2.7872.201-209

Abstract

The performance of toluene methylation reaction was studied on H-ZSM-5 catalyst modified with La, Ce and Nb at different percentage loading. It was found that 10% metal loading produced the best performance in the reaction in terms of toluene conversion. The catalyst was coated on silicon carbide foam support which showed better conversion than the pelleted catalyst. Again, among the treated and untreated H-ZSM-5, the La-ZSM-5 catalyst is chosen for the reaction for its highest selectivity towards xylene, the main product. All catalysts were characterized in terms of surface properties, SEM, XRD and NH3-TPD. Kinetic study was done on La-ZSM-5 catalyst with 10% loading. In this kineticstudy, Langmuir Hinshelwood kinetic model with surface reaction as rate controlling step was selected as the rate equation. The activation energy was found to be 47 kJ/mol. © 2015 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)
Mesoporous Silica from Rice Husk Ash V. R. Shelke; S. S. Bhagade; S. A. Mandavgane
Bulletin of Chemical Reaction Engineering & Catalysis 2010: BCREC Volume 5 Issue 2 Year 2010 (December 2010)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.5.2.795.87-93

Abstract

Mesoporous silica is used as a raw material in several areas: in preparation of catalysts, in inks, as a concrete hardening accelerator, as a component of detergents and soaps, as a refractory constituent etc. Sodium silicate is produced by reacting rice hull ash (RHA) with aqueous NaOH and silica is precipitated from the sodium silicate by acidification. In the present work, conversion of about 90% of silica contained in RHA into sodium silicate was achieved in an open system at temperatures of about 100 °C. The results showed that silica obtained from RHA is mesoporous, has a large surface area and small particle size. Rice Husk is usually mixed with coal and this mixture is used for firing boilers. The RHA therefore, usually contains carbon particles. Activated carbon embedded on silica has been prepared using the carbon already present in RHA. This carbon shows good adsorption capacity. © 2010 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)
Synthesis, Crystal Structure and Catalytic Activity of Tri-Nuclear Zn(II) Complex Based on 6-Phenylpyridine-2-carboxylic Acid and Bis(4-pyridyl)amine Ligands Li-Hua Wang; Fan-Yuan Kong; Tai Xi-Shi
Bulletin of Chemical Reaction Engineering & Catalysis 2022: BCREC Volume 17 Issue 2 Year 2022 (June 2022)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.17.2.13952.394-402

Abstract

A new trinuclear Zn (II) complex, [Zn3(L1)4(L2)2(CH3COO)2] (1) (HL1 = 6-phenylpyridine-2-carboxylic acid, L2 = bis(4-pyridyl)amine) has been synthesized by 6-phenylpyridine-2-carboxylic acid, NaOH, bis(4-pyridyl)amine and Zn(CH3COO)2•2H2O. The complex 1 has also been structural characterized by elemental analysis and single crystal X-ray diffraction. The results reveals that complex 1 is made up of three Zn(II) ions, four L1 ligands, two L2 ligands and two CH3COO- anions. In 1, both Zn1 ion and Zn1a ion are five-coordinated with two O atoms from two different L1 ligands, two N atoms from two different L1 ligands, and one N atoms from bis(4-pyridyl)amine ligand, respectively, and forms a distorted trigonal biyramid geometry. And Zn2 ion is four-coordinated with two O atoms from two different CH3COO− anions and two N atoms from two different L2 ligands, forming a distorted tetrahedral geometry. Complex 1 displays a 3D network structure by the intermolecular N−H···O hydrogen bonds. The catalytic performance for oxidation of benzyl alcohol with O2 was studied under mild reaction conditions using complex 1 as catalyst. The results demonstrated that the catalysts were very active, and the yield of benzaldehyde was 50.8% at 90 °C with THF as solvent under 0.5 MPa O2 within 3 h. Copyright © 2022 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). 
Backmatter (Publication Ethics, Copyright Transfer Agreement for Publishing Form)
Bulletin of Chemical Reaction Engineering & Catalysis 2014: BCREC Volume 9 Issue 3 Year 2014 (December 2014)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.19430

Abstract

Backmatter (Publication Ethics, Copyright Transfer Agreement for Publishing Form)

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