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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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Improved Stabilities of Immobilized Glucoamylase on Functionalized Mesoporous Silica Synthesised using Decane as Swelling Agent Reni George; Sanjay Gopinath; Sankaran Sugunan
Bulletin of Chemical Reaction Engineering & Catalysis 2013: BCREC Volume 8 Issue 1 Year 2013 (June 2013)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.8.1.4208.70-76

Abstract

Ordered mesoporous silica, with high porosity was used to immobilize glucoamylase via adsorption and covalent binding. Immobilization of glucoamylase within mesoporous silica was successfully achieved, resulting in catalytically high efficiency during starch hydrolysis. In this study, mesoporous silica was functionalized by co-condensation of tetraethoxysilane (TEOS) with organosilane (3-aminopropyl) triethoxysilane (APTES) in a wide range of molar ratios of APTES: TEOS in the presence of triblock copolymer P123 under acidic hydrothermal conditions. The prepared materials were characterized by Small angle XRD, Nitrogen adsorption – desorption and 29Si MAS solid state NMR. N2 desorption studies showed that pore size distribution decreases due to pore blockage after functionalization and enzyme immobilization. Small angle XRD and 29Si MAS NMR study reveals mesophase formation and Si environment of the materials. The main aim of our work was to study the catalytical activity, effect of pH, temperature storage stability and reusability of covalently bound glucoamylase on mesoporous silica support. The result shows that the stability of enzyme can be enhanced by immobilization.  © 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)
Thermo-Catalytic Methane Decomposition for Hydrogen Production: Effect of Palladium Promoter on Ni-based Catalysts Irene Lock Sow Mei; S.S.M. Lock; Dai-Viet N. Vo; Bawadi Abdullah
Bulletin of Chemical Reaction Engineering & Catalysis 2016: BCREC Volume 11 Issue 2 Year 2016 (August 2016)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.11.2.550.191-199

Abstract

Hydrogen production from the direct thermo-catalytic decomposition of methane is a promising alternative for clean fuel production. However, thermal decomposition of methane can hardly be of any practical and empirical interest in the industry unless highly efficient and effective catalysts, in terms of both catalytic activity and operational lifetime have been developed. In this study, the effect of palladium (Pd) as a promoter onto Ni supported on alumina catalyst has been investigated by using co-precipitation technique. The introduction of Pd promotes better catalytic activity, operational lifetime and thermal stability of the catalyst. As expected, highest methane conversion was achieved at reaction temperature of 800 °C while the bimetallic catalyst (1 wt.% Ni -1wt.% Pd/Al2O3) gave the highest methane conversion of 70% over 15 min of time-on-stream (TOS). Interestingly, the introduction of Pd as promoter onto Ni-based catalyst also has a positive effect on the operational lifetime and thermal stability of the catalyst as the methane conversion has improved significantly over 240 min of TOS. 
Simulation Study of a Membrane Reactor for Ultrapure Hydrogen Recovery from Methanol Steam Reforming Reaction under Periodic Steady-State Lemnouer Chibane
Bulletin of Chemical Reaction Engineering & Catalysis 2018: BCREC Volume 13 Issue 2 Year 2018 (August 2018)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.13.2.1340.275-285

Abstract

Steam reforming of methanol over Cu/ZnO/Al2O3 catalyst was theoretically studied under created unsteady state. A mathematical approach was proposed to evaluate the effect of periodic inputs on reactor performance. The efficacy of the periodic separating reactor in term of pure hydrogen and of methanol conversion was measured during the reaction of methanol steam reforming. The obtained results showed that under certain operating conditions the periodic operation can be used advantageously to increase the reactor ability up to a level higher than the maximal steady-state. Moreover, our findings showed that the pumping of hydrogen through the membrane was stimulated by the effect of periodic operations. The predicted results suggested that the created unsteady state mode by using a square wave function could give the better performances compared to the sinusoidal mode. 
Ceria-Based Mixed Oxide Supported Nano-Gold as an Efficient and Durable Heterogeneous Catalyst for Oxidative Dehydrogenation of Amines to Imines Using Molecular Oxygen Bashir Ahmad Dar; Meena Sharma; Baldev Singh
Bulletin of Chemical Reaction Engineering & Catalysis 2012: BCREC Volume 7 Issue 1 Year 2012 (June 2012)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.7.1.1257.79-84

Abstract

The present work is intended to determine the catalytic activity of Mixed Oxide supported gold for aerobic oxidative dehydrogenation of amines to imines using Ceria as a main constituent of the each support. The model catalysts Au/CeO2:TiO2 Au/CeO2:SiO2, Au/CeO2:ZrO2 and Au/CeO2:Al2Os were prepared by deposition co-precipitation method and deposition of gold was determined by EDEX analysis. The supported nano-gold catalyzes the dehydrogenation of secondary amines to imines without loss of activity. On recycling good amount of product yield is obtained. Oxidation of secondary amines to imines is carried at 100˚C and almost 90 % conversion was obtained with >99% selectivity. © 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)
Evaluation of Novel Integrated Dielectric Barrier Discharge Plasma as Ozone Generator Muhammad Nur; Ade Ika Susan; Zaenul Muhlisin; Fajar Arianto; Andi Wibowo Kinandana; Iis Nurhasanah; Sumariyah Sumariyah; Pratama Jujur Wibawa; Gunawan Gunawan; Anwar Usman
Bulletin of Chemical Reaction Engineering & Catalysis 2017: BCREC Volume 12 Issue 1 Year 2017 (April 2017)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.12.1.605.24-31

Abstract

This paper presents a characterization of an integrated ozone generator constructed by seven of reactors of Dielectric Barrier Discharge Plasma (DBDP). DBDP a has spiral-cylindrical configuration. Silence plasma produced ozone inside the DBDP reactor was generated by AC-HV with voltage up to 25 kV and maximum frequency of 23 kHz. As a source of ozone, dry air was pumped into the generator and controlled by valves system and a flowmeter. We found ozone concentration increased with the applied voltage, but in contrary, the concentration decreased with the flow rate of dry air. It was also found that a maximum concentration was 20 mg/L and ozone capacity of 48 g/h with an input power of 1.4 kW. Moreover, in this generator, IP efficiency of 8.13 g/kWh was obtained at input power 0.45 kW and air flow rate of 9 L/min. Therefore, be the higher ozone capacity can be produced with higher input power; however, it provided lower IP efficiency. The effect of dry air flow rate and applied voltage on ozone concentrations have been studied. At last, spiral wire copper was very corrosive done to the interaction with ozone, and it is necessary to do a research for finding the best metals as an active electrode inside of the quartz dielectric. 
1D/2D Rod-sheet Shape Bi2S3 Photocatalyst for Photocatalytic Reduction Cr(VI) under Visible Light Wu, Xinzhuo; Chen, Shaojie; Jiang, Yinxing; Zhao, Xinshan; Li, Zhao; Zhou, Yingmei; Li, Jing
Bulletin of Chemical Reaction Engineering & Catalysis 2023: BCREC Volume 18 Issue 4 Year 2023 (December 2023)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.20054

Abstract

The crystal structure and morphology of photocatalysts play a crucial role in determining their photocatalytic performance. In this study, we synthesized and investigated 1D/2D Bi2S3 as a potential visible-light-activated photocatalyst for the reduction of aqueous Cr(VI). The 1D/2D Bi2S3 was synthesized using hydrothermal synthesis technique by heating Bi2(H2O)2(SO4)2(OH)2 precursor and sodium sulfide at 190 ℃ for 24 h, where the molar ratio of Bi to S elements in the reaction reagents was changed from 1:6 to 2:3. The structure, composition, and optoelectronic properties of the prepared Bi2S3 were characterized using X-ray diffraction, UV-vis diffuse reflectance spectra, field emission scanning electron microscopy, electrochemical impedance spectra, and transient photocurrent. It is shown that the prepared orthorhombic Bi2S3 has full-spectrum photoresponsivity. Bi2S3-B with 1D/2D heterogeneous structure exhibits the lowest charge carrier transport resistance, and its photocurrent intensity is nearly twice that of Bi2S3-C. It demonstrates the highest photocatalytic activity in visible-light photocatalytic reduction of aqueous Cr(VI), with a reduction rate of 54.5% after 140 minutes of light exposure. According to the bandgap of Bi2S3 and radical scavenger experiments, a reaction mechanism for the photocatalytic reduction of Cr(VI) by Bi2S3 was proposed. Furthermore, the results highlight the economic and environmentally friendly nature of the hydrothermal synthesis method using homemade precursors, which allows for the regulation of Bi2S3 morphology and the enhancement of its visible photocatalytic activity. 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). 
Potential of LiNO3/Al2O3 Catalyst for Heterogeneous Transesterification of Palm Oil to Biodiesel Istadi Istadi; Bambang Pramudono; Suherman Suherman; Slamet Priyanto
Bulletin of Chemical Reaction Engineering & Catalysis 2010: BCREC Volume 5 Issue 1 Year 2010 (June 2010)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.5.1.7128.51-56

Abstract

Production of biodiesel through transesterification process using heterogenous catalysts in order to avoid the saponification problem was studied. In this process, palm oil reacted with methanol to form a mixture of glycerol and biodiese over a solid basic catalyst. One type of the catalysts used in this research is basic catalyst of LiNO3/Al2O3. The parameters studied in this research are concentration of LiNO3 loading on Al2O3 and effect of different reaction time. The products was analyzed using Gas Chromatography to determine composition and yield of resulted methyl esters as well as conversion of palm oil to biodiesel. The major products in this transesterification reaction were biodiesel and glycerol. It can be concluded that the 20 wt% LiNO3/Al2O3 catalyst is potential for producing biodiesel from palm oil over transesterification reaction. Advantages of the usage of this catalyst is that the soap formation was not observed in this research. © 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, Catalytic Properties, and Luminescent of a Novel Eu(III) Complex Material with 4-Imidazolecarboxaldehyde-pyridine-2-carbohydrazone Li-Hua Wang; Lei Liang; Peng-Fei Li
Bulletin of Chemical Reaction Engineering & Catalysis 2017: BCREC Volume 12 Issue 2 Year 2017 (August 2017)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.12.2.764.185-190

Abstract

A novel Eu(III) complex, [Eu(L)2(H2O)4]·(NO3)·(H2O)4 (1) (H2L = 4-imidazolecarboxaldehyde-pyridine-2-carbohydrazide), was synthesized. Its structure has been characterized by elemental analysis, IR, and X-ray single crystal diffraction analysis. Complex 1 is of orthorhombic, space group Fdd2 with a = 29.471(6) A˚, b = 10.287(2) A˚, c = 24.340(5) A˚, V = 7379(3) A˚3, Z = 8, Mr = 902.58, Dc = 1.625 µg·m-3, µ = 1.789 mm-1, F(000) = 3656, GOOF = 1.099, the final R= 0.0517, ωR= 0.1292 for 3043 observed reflections with I > 2σ(I).  The A3 coupling reaction has been investigated using the complex 1 as catalyst. The luminescent spectrum of the complex 1 gives two weak peaks (448 nm and 491 nm) and two strong peaks (596 nm and 620 nm) from excitation at 279 nm. 
Synthesis of Metal-Organic Framework (MOF) Cr-PTC-HIna for Heavy Metal Ion Adsorption Nurhasni, Nurhasni; Adawiah, Adawiah; Wahyudin, Wahyudin; Hadriyani, Rizka; Andriyani, Leni; Fadhilla, Rizkha; Zulys, Agustino; Sukandar, Dede
Bulletin of Chemical Reaction Engineering & Catalysis 2024: BCREC Volume 19 Issue 1 Year 2024 (April 2024)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.20069

Abstract

As an adsorbent material, Metal-Organic Framework (MOF) provides several advantages, such as large surface area and pore volume, as well as stability in aqueous systems both in acidic, basic, and neutral conditions. The research successfully made a metal organic framework (MOF) from chromium and perylene that was modulated by isonicotinic acid. This was done using three different methods: hydrothermal (Cr-PTC-HIna-HT), solvothermal (Cr-PTC-HIna-ST), and sonochemical (Cr-PTC-HIna-SC). The Cr-PTC-HIna-SC showed the greatest Pb2+ ion adsorption capacity. The optimum adsorption of Pb2+ ions occurred at 150 ppm Pb2+ ion concentration, pH 5, 90 minutes of contact time, and an adsorption capacity of 149.95 mg/g at 35 °C. The dominant adsorption isotherm model is the Langmuir isotherm model with R2 = 0.9867 and follows the pseudo-second-order. The selectivity test showed that Cr-PTC-HIna-SC MOF could adsorb more Cd2+ ions than Pb2+ ions, with 250 mg/g being the best amount.
Highly Active W-H2SO4/HZSM-5 Catalyst for Direct Conversion of Methane into Aromatic Kusmiyati Kusmiyati; N. A. S. Amin; W. A. Siswanto
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.2.2-3.7.32-36

Abstract

Dehydroaromatization of methane (DHAM) under non oxidative condition was studied over tungsten loaded HZSM-5 catalysts to produce aromatic hydrocarbons. The catalysts were prepared by impregnation method using different conditions : in neutral and acidified solution. The activity of W/HZSM-5 prepared by neutral solution and W-H2SO4/HZSM-5 prepared in acidified condition were compared. The results showed that the optimum activity of W-H2SO4/HZSM-5 catalyst exceeded that of W/HZSM-5 catalyst. The effect of Si/Al ratio of W-H2SO4/HZSM-5 catalyst was also studied. The W-H2SO4/HZSM-5 catalyst with Si/Al ratio = 0 was found to be the most promising for the DHAM reaction. The remarkable activity of the catalyst is attributed to the presence of dual effects: suitable content of octahedral polymeric and tetrahedral monomeric tungstate species accompanied by proper amount and strength of acid sites in the catalyst. © 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)

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