cover
Contact Name
Istadi
Contact Email
istadi@che.undip.ac.id
Phone
+6281316426342
Journal Mail Official
bcrec@live.undip.ac.id
Editorial Address
Editorial Office of Bulletin of Chemical Reaction Engineering & Catalysis Laboratory of Plasma-Catalysis (R3.5), UPT Laboratorium Terpadu, Universitas Diponegoro Jl. Prof. Soedarto, Semarang, Central Java, Indonesia 50275
Location
Kota semarang,
Jawa tengah
INDONESIA
Bulletin of Chemical Reaction Engineering & Catalysis
ISSN : -     EISSN : 19782993     DOI : https://doi.org/10.9767/bcrec
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.
Articles 686 Documents
Esterification of Benzyl Alcohol with Acetic Acid over Mesoporous H-ZSM-5 Desy Tri Kusumaningtyas; Didik Prasetyoko; Suprapto Suprapto; Sugeng Triwahyono; Aishah Abdul Jalil; Afifah Rosidah
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.12.2.806.243-250

Abstract

In this study, the performance of mesoporous ZSM-5 has been studied on the esterification of acetic acid (AA) with benzyl alcohol (BA). The mesoporous ZSM-5 catalyst has been synthesized with the variation of aging time i.e. 6, 12, and 24 hours at the same temperature, 70 °C. The cation exchange of Na-ZSM-5 to H-ZSM-5 was performed before the catalytic activity test. The acidity type and amount of solids were determined by FT-IR spectroscopy using pyridine as a probe molecule. The characterization by pyridine adsorption showed that at a higher mesoporous surface area, the number of Lewis acid was increased. The highest mesoporous surface area, Lewis, and Brönsted acid sites were obtained by sample which has the lowest crystallinity, i.e. 255.78 m2/g, 0.2732 mmol/g, and 0.20612 mmol/g, respectively. Influence of mesoporous volume was studied on the catalytic activity of the mesoporous ZSM-5 in the esterification reaction. Conversion of acetic acid in the esterification reaction for samples of    HZ-6, HZ-12, and HZ-24 were obtained by titration methods, i.e. 39.59, 36.39, and 32.90 %, respectively. Hence, the reaction temperature of 393 K, molar ratio 1:4 (AA:BA) and catalyst loading 5 % were selected as an optimum reaction parameters. 
Synthesis of Spherical Nanostructured g-Al2O3 Particles using Cetyltrimethylammonium Bromide (CTAB) Reverse Micelle Templating Didi Prasetyo Benu; Veinardi Suendo; Rino Rakhmata Mukti; Erna Febriyanti; Fry Voni Steky; Damar Rastri Adhika; Viny Veronika Tanuwijaya; Ashari Budi Nugraha
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.14.3.3855.542-550

Abstract

We demonstrated the synthesis of spherical nanostructured g-Al2O3 using reverse micelle templating to enhance the surface area and reactant accessibility. Three different surfactants were used in this study: benzalkonium chloride (BZK), sodium dodecyl sulfate (SDS) and cetyltrimethylammonium bromide (CTAB). We obtained spherical nanostructured particles only using CTAB that form a reverse micelle emulsion. The particles have wide size distribution with an average size of 2.54 mm. The spherical particles consist of nanoplate crystallites with size 20-40 nm randomly arranged forming intercrystallite spaces. The crystalline phase of as-synthesized and calcined particles was boehmite and g-Al2O3, respectively as determined by XRD analysis. Here, the preserved particle morphology during boehmite to g-Al2O3 transformation opens a facile route to synthesize g-Al2O3 particles with complex morphology. The specific surface area of synthesized particles is 201 m2/g, which is around five times higher than the conventional g-Al2O3 (Aldrich 544833). Spherical nanostructured g-Al2O3 provides wide potential applications in catalysis due to its high density closed packed structure, large surface area, and high accessibility. 
A Review on Diesel Soot Emission, its Effect and Control Ram Prasad; Venkateswara Rao Bella
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.5.2.794.69-86

Abstract

The diesel engines are energy efficient, but their particulate (soot) emissions are responsible of severe environmental and health problems. This review provides a survey on published information regarding diesel soot emission, its adverse effects on the human health, environment, vegetations, climate, etc. The legislations to limit diesel emissions and ways to minimize soot emission are also summarized. Soot particles are suspected to the development of cancer; cardiovascular and respiratory health effects; pollution of air, water, and soil; impact agriculture productivity, soiling of buildings; reductions in visibility; and global climate change. The review covers important recent developments on technologies for control of particulate matter (PM); diesel particulate filters (DPFs), summarizing new filter and catalyst materials and DPM measurement. DPF technology is in a state of optimization and cost reduction. New DPF regeneration strategies (active, passive and plasma-assisted regenerations) as well as the new learning on the fundamentals of soot/catalyst interaction are described. Recent developments in diesel oxidation catalysts (DOC) are also summarized showing potential issues with advanced combustion strategies, important interactions on NO2 formation, and new formulations for durability. Finally, systematic compilation of the concerned newer literature on catalytic oxidation of soot in a well conceivable tabular form is given. A total of 156 references are cited. © 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)
Insights into the Titania (TiO2) Photocatalysis on the Removal of Phthalic Acid Esters (PAEs) in Water Norfarahim Mohd Tubillah; Sheela Chandren
Bulletin of Chemical Reaction Engineering & Catalysis 2022: BCREC Volume 17 Issue 3 Year 2022 (September 2022)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.17.3.15385.608-626

Abstract

In this era of globalization, plastic is regarded as one of the most versatile innovations, finding its uses ranging from packaging, automotive, agriculture, and construction to the medical and pharmaceutical industries. Unfortunately, the single-use nature of plastics leads to ecological and environmental problems. Among conventional disposal management of plastic waste are landfilling dumping, incineration, and recycling. However, not all plastic waste goes into disposal management and ends up accumulating in lakes, rivers, and seas. In the aquatic environment, the action of photochemical weathering plastics has resulted in the release of chemical additives such as phthalic acid esters (PAEs), an important plasticizer added to plastic products to improve their softness, flexibility, and durability. Nowadays, PAEs have been ubiquitously detected in our environment and numerous organisms are exposed to PAEs to some extent. As PAEs carry endocrine disruptive and carcinogenicity properties, an urgent search for the development of an efficient and effective method to remove PAEs from the environment is needed. As a viable option, titania (TiO2) photocatalysis is a promising tool to combat the PAEs contamination in our environment owing to its high photocatalytic activity, cost-effectiveness, and its ability to totally mineralize PAEs into carbon dioxide and water. Hence, this paper aims to highlight the concerning issue of the contamination of PAEs in our aquatic environments and the summary of the removal of PAEs by TiO2 photocatalysis. This review concerning the significance of knowledge on environmental PAEs would hopefully spark huge interest and future development to tackle this plastic-associated pollutant. 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). 
Hydrocracking of Calophyllum inophyllum Oil Employing Co and/or Mo Supported on γ-Al2O3 for Biofuel Production Wega Trisunaryanti; Triyono Triyono; Mohammad Ali Ghoni; Dyah Ayu Fatmawati; Puspa Nindro Mahayuwati; Endah Suarsih
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.15.3.8592.743-751

Abstract

Cobalt and/or Molybdenum based catalysts were simply dispersed on γ-Al2O3 through wet impregnation. The set of prepared monometallic and bimetallic catalysts of aCoO/γ-Al2O3, aMoO/γ-Al2O3, aCoOaMoO/γ-Al2O3, and bCoObMoO/γ-Al2O3 were investigated and evaluated in the hydrocracking of Calophyllum inophyllum (CIO) which is not a food crop as well as rich in unsaturated fatty acid that potential to be converted into biofuel. Out of the prepared catalysts, aCoOaMoO/γ-Al2O3 with total   metal content, acidity, and specific surface area of 13.62 wt%, 5.01 mmol.g-1, and 107.67 m2.g-1, respectively, showed the best catalytic performance. The high metal loading of aCoOaMoO/γ-Al2O3is favorable by producing 65.56 wt% liquid fraction through carbocation formation mechanism. It was selective to produce 8.61 wt% gasoline and 5.01 wt% diesel. 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). 
Design of a Simple and Cheap Water Electrolyser for the Production of Solar Hydrogen Ram Prasad
Bulletin of Chemical Reaction Engineering & Catalysis 2009: BCREC Volume 4 Issue 1 Year 2009 (June 2009)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.4.1.7113.10-15

Abstract

Commercially available conventional alkaline electrolyser and advanced polymer membrane electrolysers for water electrolysis are quite expensive. Taking into account this aspect, a very simple and cheap water electrolyser has been designed and fabricated utilising easily available economical materials for small scale production of hydrogen using renewable energy from photovoltaic panel. The construction details of the electrolyser with a schematic drawing of the experimental set-up for PV production of H2 are given. In order to fabricate the compact electrolyser, two coaxial tubular PVC pipes were used. The lower part of the inner pipe has fine perforations for the transport of ions through electrolyte between the electrodes. Two cylindrical electrodes, cathode and anode are kept in inner and outer pipes respectively. The performance of hydrogen production was measured using a photovoltaic panel directly connected to the electrolyser under atmospheric pressure and in 27wt% KOH solution. Flow rates of hydrogen and oxygen were measured using a digital flow meter. High purity fuel cell grade hydrogen (99.98%) and oxygen (99.85%) have been produced. The experimental results confirm that the present electrolyser has eligible properties for hydrogen production in remote areas. No such electrolyser has been reported prior to this work. © 2009 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)
Photocatalytic Degradation of Remazol Brilliant Blue R and Remazol Yellow FG using TiO2 doped Cd, Co, Mn Candra Purnawan; Sayekti Wahyuningsih; Oktaviani Nur Aniza; Octaria Priwidya Sari
Bulletin of Chemical Reaction Engineering & Catalysis 2021: BCREC Volume 16 Issue 4 Year 2021 (December 2021)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.16.4.11423.804-815

Abstract

TiO2 and TiO2 doped Cd, Co, Mn (TiO2-M) were synthesized with a sol-gel method, and the photocatalytic activity of Remazol Brilliant Blue R and Remazol Yellow FG has been conducted. TiO2-M (Cd, Co, Mn) was synthesized with the mol Ti:M ratio of 3:1, and the materials were calcined at 300, 400, and 500 °C. The materials were characterized by X-ray Diffraction (XRD), Scanning Electron Microscopy-Energy Dispersive X-ray (SEM-EDX), and UV-Vis Reflectance. The XRD result shows that at the temperature of 300 °C TiO2 and TiO2-M formed tend to be amorphous. At 400 °C the anatase phase is formed, while at 500 °C the rutile phase begins to form. And overall, the crystallinity of TiO2 is higher than metal-doped TiO2. The UV-Vis Reflectance result showed that the bandgap energy of all doping materials (TiO2-M) decreased. The larger the metal ion radius of dopant, the larger the crystal size obtained  and then the higher the bandgap obtained. The results of SEM-EDX showed that the morphology of TiO2 was spherical and regular, whereas the morphology of TiO2-M had a smoother surface due to the influence of metal doping. Photocatalytic activity of TiO2-M on Remazol Brilliant Blue R and Remazol Yellow FG was greater than TiO2. The optimum pH of the solution was obtained at pH 5 and the optimum catalyst phase was obtained at the anatase phase. The percentages degradation for 30 min of Remazol Brilliant Blue R were 67.34% (TiO2), 92.12% (TiO2-Co), 85.47% (TiO2-Mn), and 83.91% (TiO2-Cd), while for Remazol Yellow FG they were 58.84% (TiO2), 74.61% (TiO2-Co), 67.93% (TiO2-Mn) and 64.19% (TiO2-Cd), respectively. 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). 
Production of High-Octane Number Gasoline from Basra Low Octane-Number Gas Condensate and Ethanol over Modified Zn/ZSM5 Zeolite Catalyst Mohammed Abdulrazzaq Salim; Usama Akram Saed
Bulletin of Chemical Reaction Engineering & Catalysis 2023: BCREC Volume 18 Issue 1 Year 2023 (April 2023)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.16763

Abstract

Catalytic transformation of a low-octane number stable gas condensate to high-octane number gasoline (RON: research octane number) is an economically and strategically vital process. In this research, modifying ZSM5 zeolite (80 Si/Al ratio) by impregnation with 2% Zn (Zn/ZSM5) was carried out to increase the selectivity for isomerization and aromatization thereby enhance the octane number. The process was conducted by using stable gas condensate 85 vol% with 15 vol% ethanol in a fixed bed reactor. Zn/ZSM5 and ZSM5 were examined in a pilot scale under different conditions temperature 360-420 °C LHSV1.2-2 h−1, pressure 5 bar. Catalysts were characterized before and after Zn loading using Fourier Transform Infra Red (FT-IR), Brunauer-Emmett-Teller (BET), X-ray Diffraction (XRD), Scanning Electron Microscope (SEM), Field Emission Scanning Electron Microscope (FESEM), Transmission Electron Microscope (TEM), and N2-adsorption. The SEM, FESEM, and TEM have shown that no change in morphology and metal distribution. The XRD and FTIR characterizations revealed the modified catalysts retained their crystallinity after metal impregnation while N2-adsorption isotherm demonstrates no significant change in porosity. The results of Zn/ZSM5 display an optimum result at 420 °C, 1.2 h−1, 5 bar with enhancement of RON from 60.5 to 89 whereas ZSM5 shows RON enhancement from 60.5 to 82. Post Zn loading, PONA test has shown an increase for iso-paraffin from 45.4 to 47.4%, and aromatics from 10.8 to 14. The findings translate the effectiveness of using Zn on ZSM5 for gas condensate – gasoline transformation. 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). 
Controlled Synthesis of Silver Nanoparticles Using Double Reductants and Its Voltammetric Characteristics Study Yubo Duan; Zhihua Xu; Xiaochun Jiang
Bulletin of Chemical Reaction Engineering & Catalysis 2016: BCREC Volume 11 Issue 1 Year 2016 (April 2016)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.11.1.433.115-119

Abstract

Constructing robust silver nanoparticles (AgNPs) with good shape and dispersibility is of particular interest in analytical applications. Herein, monodispersibility AgNPs with the average size of 20 nm have been successfully prepared via one-pot method using sodium borohydride and trisodium citrate as co-reductants. The introduction of sodium borohydride greatly accelerated the rate of nucleation, which can effectively solve the problem of broad size distribution. Both shape and dispersibility of AgNPs can be effectively adjusted by simple control of refluxing time or concentrations of the sodium borohydride. We also studied the voltammetric characteristics of the AgNPs using Ag/AgCl solid-state voltammetry. An intense and stable current peak at a low potential could be obtained, which could provide a unique advantage in analytical applications. 
Highly Sensitive Electrocatalytic Determination of Formaldehyde Using a Ni/Ionic Liquid Modified Carbon Nanotube Paste Electrode Ebrahim Zarei; Mohammad Reza Jamali; Farideh Ahmadi
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.13.3.2341.529-542

Abstract

In this study, ionic liquid 1-hexyl-3-methylimidazolium hexafluorophosphate was applied as additives to fabricate a novel ionic liquid/carbon nanotube paste electrode (IL/CNPE). This electrode was characterized by electrochemical impedance spectroscopy and cyclic voltammetry. Results showed that the electron transfer rate and reversibility of the electrode were increased by the ionic liquid. The morpho-logy of prepared IL/CNPE was studied by scanning electron microscopy. Nickel/ionic liquid modified carbon nanotube paste electrode (Ni/IL/CNPE) was also constructed by immersion of the IL/CNPE in nickel sulfate solution. Ionic liquid showed significant effect on the accumulation of nickel species on the surface of the electrode. Also, the values of electron transfer coefficient, charge-transfer rate constant and electrode surface coverage for Ni(II)/Ni(III) redox couple of the Ni/IL/CNPE were found to be 0.32 and 2.37×10-1 s-1 and 2.74×10-8 mol.cm-2, respectively. The Ni/IL/CNPE was applied successfully to highly efficient electrocatalytic oxidation of formaldehyde in alkaline medium. The effects of various factors on the efficiency of electrocatalytic oxidation of formaldehyde were optimized. Under the optimized condition, cyclic voltammetry of formaldehyde at the modified electrode exhibited two linear dynamic ranges in the concentration ranges of 7.00×10-6 to 9.60×10-5 mol.L-1 and 9.60×10-5 to 32.00×10-3 mol.L-1 with excellent detection limit of 9.50×10-7 mol.L-1 (3σ/slope), respectively. Also, the method was successfully applied for formaldehyde measurement in real sample. 

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