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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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Highly Selective Au/ZnO via Colloidal Deposition for CO2 Hydrogenation to Methanol: Evidence of AuZn Role Hasliza Bahruji; Mshaal Almalki; Norli Abdullah
Bulletin of Chemical Reaction Engineering & Catalysis 2021: BCREC Volume 16 Issue 1 Year 2021 (March 2021)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.16.1.9375.44-51

Abstract

Gold, Au nanoparticles were deposited on ZnO, Al2O3, and Ga2O3 via colloidal method in order to investigate the role of support for CO2 hydrogenation to methanol. Au/ZnO was also produced using impregnation method to investigate the effect of colloidal method to improve methanol selectivity. Au/ZnO produced via sol immobilization showed high selectivity towards methanol meanwhile impregnation method produced Au/ZnO catalyst with high selectivity towards CO. The CO2 conversion was also influenced by the amount of Au weight loading. Au nanoparticles with average diameter of 3.5 nm exhibited 4% of CO2 conversion with 72% of methanol selectivity at 250 °C and 20 bar. The formation of AuZn alloy was identified as active sites for selective CO2 hydrogenation to methanol. Segregation of Zn from ZnO to form AuZn alloy increased the number of surface oxygen vacancy for CO2 adsorption to form formate intermediates. The formate was stabilized on AuZn alloy for further hydrogenation to form methanol.  The use of Al2O3 and Ga2O3 inhibited the formation of Au alloy, and therefore reduced methanol production. Au/Al2O3 showed 77% selectivity to methane, meanwhile Au/Ga2O3 produced 100% selectivity towards CO. 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). 
Synergistic Corrosion Inhibition Effect of Rice Husk Extract and KI for Mild Steel in H2SO4 Solution Marta Pramudita; Sukirno Sukirno; Mohammad Nasikin
Bulletin of Chemical Reaction Engineering & Catalysis 2019: BCREC Volume 14 Issue 3 Year 2019 (December 2019)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.14.3.4249.697-704

Abstract

The corrosion inhibition of rice husk extract for bio-corrosion in mild steel in 1 M of H2SO4 solution and the effect of adding potassium iodide were investigated using the weight-loss method with a variable solution temperature and various bio-inhibitor concentrations. The addition of potassium iodide can significantly increase the efficiency of rice husk extract. The highest efficiency is 95.89% at 1,250 ppm of inhibitor concentration at a temperature of 313 K. The inhibition efficiency of rice husk extract is synergistically increased with the addition of potassium iodide. The characteristics of the adsorption inhibitors were assessed using the Langmuir isotherm adsorption approach at all studied concentrations and temperatures. The synergy of rice husk extract and potassium iodide was examined using thermodynamic and kinetic parameters. 
The Effect of Time on the Activation of Bayah Natural Zeolite for Application of Palm Oil Shell Pyrolysis Endang Suhendi; Teguh Kurniawan; Adian Yoga Pradana; Vicky Zayan Giffari
Bulletin of Chemical Reaction Engineering & Catalysis 2021: BCREC Volume 16 Issue 3 Year 2021 (September 2021)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.16.3.10313.588-600

Abstract

Oil palm shell (OPS) constitutes 60% of the waste generated during the processing of palm oil. However, OPS can potentially be converted into energy and chemicals through pyrolysis. The purpose of this study is to determine and analyse the effect of acid treatment time on the characteristics of natural zeolites, which were then applied to oil palm shell pyrolysis. The effect of the acid treatment time on the products of the pyrolysis was also studied. The acid treatment time was varied: 1, 3, and 5 hours. The crystallinity of the natural zeolites was determined by       X-ray diffraction (XRD). Solid, liquid and gaseous pyrolysis products were observed. Proximate, ultimate, and heat analysis were performed on the solid product. The liquid product was characterised using gas chromatography-mass spectrometry (GC-MS). Gas Chromatography (GC) was performed to analyse the composition of the gases produced. The results obtained from this study indicate that longer reflux times reduced the crystallinity of the zeolites. The addition of the zeolite catalysts increased the liquid products of pyrolysis from 24.5 wt% over the parent to 24.6–37.1 wt% over the acid-treated natural zeolites. The reduction of oxygenated compounds in bio-oil was observed in the amount of acetic acid and acetone produced. 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). 
Activity Evaluation of CoMo Nanoparticles Supported on Meso-microporous Composites in Dibenzothiophene Hydrodesulphurization Nastaran Parsafard; Mohammad Hasan Peyrovi; Zahra Mohammadian; Niloofar Atashi
Bulletin of Chemical Reaction Engineering & Catalysis 2020: BCREC Volume 15 Issue 1 Year 2020 (April 2020)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.15.1.5556.112-118

Abstract

CoMo-supported mesoporous catalysts were synthesized by 50 wt% of HZSM-5 and 50 wt% of FSM-16, KIT-6, and MCM-48. These catalysts were prepared by the wet-impregnation method and pre-sulfided with CS2. The catalytic performance was evaluated for HDS reaction of dibenzothiophene over a temperature range of 250-400 °C in a micro fixed-bed reactor under atmospheric pressure. The supported CoMo bimetallic catalysts were characterized by XRD, XRF, FT-IR, N2 adsorption-desorption, and SEM. The CoMo/KIT-6/HZSM-5 indicate higher activity than other catalysts at 400 °C for dibenzothiophene hydrodesulphurization. Also, the best selectivity to cyclohexylbenzene (CHB) is related to CoMo/FSM-16/HZSM-5. The activation energy was also calculated for all prepared catalysts for the conversions of less than 10%; according to which, the activation energy for CoMo/KIT-6/HZSM-5 is less than other catalysts (~21 kJ/mol) which can be related to the appropriate pore size and high surface area of the support. Copyright © 2020 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). 
Preparation Titanium Dioxide Combined Hydrophobic Polymer with Photocatalytic Self-Cleaning Properties Sayekti Wahyuningsih; Rochmad E. Cahyono; Fitri N. Aini
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.15.3.9225.874-884

Abstract

Titanium dioxide (TiO2) and hydrophobic of TiO2/PDMS (PDMS = polydimethylsiloxane) have been prepared as photocatalytic self-cleaning materials. Synthesis of TiO2 was carried out using the sol-gel method with titanium(IV) isopropoxide (TTIP) as a precursor and acetic acid as a solvent at a temperature of about 10–15 °C, while the synthesis of hydrophobic of TiO2/PDMS composites was carried out by a sonication method under ethanol solution. The results of XRD analysis of synthesized TiO2 showed that TiO2 was anatase phase. The glass-coated TiO2/PDMS were prepared by dip-coating under an ultrasonication bath. TiO2/PDMS composites at a ratio of TiO2/PDMS (1) on the glass plate showed hydrophobic properties, as evidenced by the contact angle of 104° before irradiation and the contact angle of 99.7° after irradiation. The synthesized titanium dioxide has irregular spherical morphology. The increase in PDMS content was correlated with an increase in the roughness of TiO2. PDMS not only acts as low surface energy but also binds TiO2. The hydrophobic behavior of PDMS creates TiO2/PDMS repel each other, gain irregular agglomeration structures. Beside having optimum contact angle, glass-coated TiO2/PDMS (1) is the best composition for degradation of methylene blue in 69.68% for 20 minutes irradiation. 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). 
Backmatter (Publication Ethics, Copyright Transfer Agreement Form)
Bulletin of Chemical Reaction Engineering & Catalysis 2019: BCREC Volume 14 Issue 2 Year 2019 (August 2019)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.14.2.4855.App.7-App.10

Abstract

Oxytetracycline Mineralization inside a UV/H2O2 System of Advanced Oxidation Processes: Inorganic By-Product Anisa Ur Rahmah; Sabtanti Harimurti; Kiki Adi Kurnia; Abdul Aziz Omar; Thanabalan Murugesan
Bulletin of Chemical Reaction Engineering & Catalysis 2021: BCREC Volume 16 Issue 2 Year 2021 (June 2021)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.16.2.10308.302-309

Abstract

Oxytetracycline (OTC) was widely used antibiotic in agricultural industry. However, most of them were secreted from the body and entered the water stream, due to low absorption. The occurrence of the antibiotics in water stream may led to serious health hazards. Hence, finding the effective method that capable to achieve total mineralization of antibiotic-contaminated wastewater, followed by the production of benign inorganic and organic by-product, was necessarily deemed. Photochemical degradation method, such as: UV/H2O2 system, was capable to achieve total mineralization of OTC at its optimized condition. In this paper, inorganic by-products of OTC mineralization inside a UV/H2O2 system at its optimum condition were analyzed. The presence of nitrate, ammonium, chloride ions, and chlorine were detected at the sample solution after mineralization. The presence of these inorganic by-product has proven that the experimental setup chosen was capable to achieve total mineralization. In addition, possible routes of the inorganic by-products detachment from the OTC’s structure, were also presented. 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). 
Catalytic Study of the Partial Oxidation Reaction of Methanol to Formaldehyde in the Vapor Phase Mohammad Hasan Peyrovi; Nastaran Parsafard; Hosein Hasanpour
Bulletin of Chemical Reaction Engineering & Catalysis 2018: BCREC Volume 13 Issue 3 Year 2018 (December 2018)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.13.3.2048.520-528

Abstract

In the present work, several parameters affecting on the catalytic behavior were studied in the process of partial oxidation of methanol to formaldehyde, such as: Mo/Fe ratio in unsupported catalysts, weight percent of the metallic phase in the supported catalysts, the effect of different supports, the method of Mo-Fe deposition on the supports, and the stability of the prepared catalysts against coke. These catalysts were characterized by X-ray diffraction (XRD), Fourier Transform Infra Red (FT-IR), Thermogravimetric Analysis (TGA), Scanning Electron Microscopy (SEM), N2 adsorption-desorption, and Atomic Adsorption Spectroscopy (AAS) methods. The best results (the methanol conversion = 97 % and formaldehyde selectivity = 96 %) were obtained for Mo-Fe/g-Al2O3 prepared by co-precipitation method with Mo/Fe = 1.7, 50 wt.% of Fe-Mo phase, 2 mL/h methanol flow rate, and 120 mL/min air flow rate at 350 oC. 
Study of the Interaction of Heavy Metals (Cu(II), Zn(II)) Ions with a Clay Soil of the Region of Naima-Tiaret-Algeria Taibi Mohamed; Elaziouti Abdelkader; Laouedj Nadjia; Dellal Abdelkader
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.15.3.8773.765-785

Abstract

The RM (RM stands for the pristine clay) collected from sites in the Naima-Tiaret-Algeria and its purified phase TM (TM stands for the treated clay) were characterized using XRF, XRD, FT−IR, SEM−EDX, and DC electrical conductivity techniques. The as-prepared clays were used as potential adsorbents for the removal of Cu2+ and Zn2+ metals ions. Highly purified clay TM, exhibiting a basal, spacing of 25.83 Å and CEC of 51 meq/100 g, was obtained. The type of interstratified I/M in the studied sites is S=1, based on the calculation method of Watanabe. The percentage of illite type S=1 is between 80−85% illite. The adsorption equilibrium was established in 60 min with the capacities of 28.57 and 24.39 mg/g for Cu2+ onto RM, 32.25 and 4.95 mg/g for Zn2+ in the presence of TM. D-R isotherm model was more suitable with the adsorption process than Freundlich and Langmuir models suggesting the ion exchange nature of the retention mechanism in most cases (E > 8 kJ/mol). Pseudo second-order model best described the kinetics of adsorption process. The adsorption mechanism was mainly monitored by ion exchange mechanism between exchangeable interlayer cations (Na) in the interstratified I/M and Cu2+ or Zn2+ metals from aqueous matrix. Further, the release of H+ ions from the edge of the layer structure in acidic environments promote the adsorption of heavy metals onto the surfaces interstratified I/M clay soils via electrostatic attraction. 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). 
Effects of Ion Exchange Process on Catalyst Activity and Plasma-Assisted Reactor Toward Cracking of Palm Oil into Biofuels Istadi Istadi; Luqman Buchori; Didi Dwi Anggoro; Teguh Riyanto; Anindita Indriana; Chusnul Khotimah; Fachmy Adji Pangestu Setiawan
Bulletin of Chemical Reaction Engineering & Catalysis 2019: BCREC Volume 14 Issue 2 Year 2019 (August 2019)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.14.2.4257.459-467

Abstract

Biofuels can be produced through a conventional catalytic cracking system and/or a hybrid catalytic-plasma cracking system. This paper was focused on studying effect of Na+ ion exchange to HY-Zeolite catalyst on catalyst performance to convert palm oil into biofuels over a conventional continuous fixed bed catalytic cracking reactor and comparing the catalytic cracking performance when carried out in a continuous hybrid catalytic-plasma reactor. The catalysts were characterized by X-ray Diffraction (XRD) and Bruneuer-Emmet-Teller (BET) surface area methods. The biofuels product were analyzed using Gas Chromatography-Mass Spectrometry (GC-MS) to determine the hydrocarbons composition of biofuels product. From the results, ion exchange process of Na+ into HY-Zeolite catalyst decreases the catalyst activity due to decreasing the number of active sites caused by blocking of Na+ ion. The selectivity to gasoline ranges achieved 34.25% with 99.11% total conversion when using HY catalyst over conventional continuous fixed bed reactor system. Unfortunately, the selectivity to gasoline ranges decreased to 13.96% and the total conversion decrease slightly to 98.06% when using NaY-Zeolite catalyst. As comparison when the cracking reaction was carried out in a hybrid catalytic-plasma reactor using a spent residual catalytic cracking (RCC) catalyst, the high energetics electron from plasma can improve the reactor performance, where the conversion and yield were increased and the selectivity to lower ranges of hydrocarbons was increased. However, the last results were potential to be intensively studied with respect to relation between reactor temperature and plasma-assisted catalytic reactor parameters. Copyright © 2019 BCREC Group. All rights reserved 

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