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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 838 Documents
Syngas Production from Catalytic CO2 Reforming of CH4 over CaFe2O4 Supported Ni and Co Catalysts: Full Factorial Design Screening M. Anwar Hossain; Bamidele Victor Ayodele; Chin Kui Cheng; Maksudur R Khan
Bulletin of Chemical Reaction Engineering & Catalysis 2018: BCREC Volume 13 Issue 1 Year 2018 (April 2018)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.13.1.1197.57-73

Abstract

In this study, the potential of dry reforming reaction over CaFe2O4 supported Ni and Co catalysts were investigated. The Co/CaFe2O4 and Ni/CaFe2O4 catalysts were synthesized using wet impregnation method by varying the metal loading from 5-15 %. The synthesized catalysts were tested in methane dry reforming reaction at atmospheric pressure and reaction temperature ranged 700-800 oC. The catalytic performance of the catalysts based on the initial screening is ranked as 5%Co/CaFe2O4 < 10%Co/CaFe2O4 < 5%Ni/CaFe2O4 < 10%Ni/CaFe2O4 according to their performance. The Ni/CaFe2O4 catalyst was selected for further investigation using full factorial design of experiment. The interaction effects of three factors namely metal loading (5-15 %), feed ratio (0.4-1.0), and reaction temperature (700-800 oC) were evaluated on the catalytic activity in terms of CH4 and CO2 conversion as well as H2 and CO yield. The interaction between the factors showed significant effects on the catalyst performance at metal loading, feed ratio and reaction temperature of 15 %, 1.0, and 800 oC. respectively. The 15 wt% Ni/CaFe2O4 was subsequently characterized by Thermogravimetric (TGA), X-ray Diffraction (XRD), Field Emission Scanning Electron Microscopy (FESEM), Energy Dispersive X-ray Spectroscopy (EDX), X-ray Photoelectron Spectroscopy (XPS), N2-physisorption, Temperature Programmed Desorption (TPD)-NH3, TPD-CO2, and Fourier Transform Infra Red (FTIR) to ascertain its physiochemical properties.  This study demonstrated that the CaFe2O4 supported Ni catalyst has a good potential to be used for syngas production via methane dry reforming. 
Comparative Study of Various Preparation Methods of CuO–CeO2 Catalysts for Oxidation of n–Hexane and iso–Octane A. Mishra; B. D. Tripathi; A. K. Rai; R. Prasad
Bulletin of Chemical Reaction Engineering & Catalysis 2013: BCREC Volume 7 Issue 3 Year 2013 (March 2013)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.7.3.4076.172-178

Abstract

The complete oxidation of n-Hexane and iso-Octane was studied individually in a fixed bed tubular flow reactor over CuO-CeO2 catalysts synthesized via four different methods namely urea-nitrate combustion method, urea gelation/co-precipitation method, citric acid sol-gel method and co-impregnation method. Laser diffraction was employed in catalysts characterization. The results obtained from the complete conversion of n-Hexane and iso-Octane revealed that the CuO-CeO2 catalysts prepared by urea-nitrate combustion method (UNC) showed the best performance than the catalysts prepared by other methods used in the present investigation. CuO-CeO2 catalysts prepared by UNC method achieve total n-Hexane and iso-Octane conversion to CO2 at lower temperatures of 280 0C and 340 0C respectively due to the larger surface area of the catalysts which increases the specific rate of reaction. © 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)
Author Guideline (2018)
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.13.3.3545.App.1-App.6

Abstract

Samarium Promoted Ni/Al2O3 Catalysts for Syngas Production from Glycerol Pyrolysis Mohd Nasir Nor Shahirah; Bamidele V. Ayodele; Jolius Gimbun; Chin Kui Cheng
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.11.2.555.238-244

Abstract

The current paper reports on the kinetics of glycerol reforming over the alumina-supported Ni catalyst that was promoted with rare earth elements. The catalysts were synthesized via wet impregnation method with formulations of 3 wt% Sm-20 wt% Ni/77 wt% Al2O3. The characterizations of all the as-synthesized catalysts were carried out, viz.  BET specific surface area measurements, thermogravimetri analysis for temperature-programmed calcination studies, FESEM for surface imaging, XRD to obtain diffraction patterns, XRF for elemental analysis, etc.. Reaction studies were performed in a stainless steel fixed bed reactor with reaction temperatures set at 973, 1023 and 1073 K employing weight hourly space velocity (WHSV) of 4.5×104 mL g-1 h-1. Agilent GC with TCD capillary column was used to analyze gas compositions. Results gathered showed that the BET specific surface area was 2.09 m2.g-1 for the unpromoted Ni catalyst while for the promoted catalysts, was 2.68 m2.g-1. Significantly, the BET results were supported by the FESEM images which showed promoted catalysts exhibit smaller particle size compared to the unpromoted catalyst. It can be deduced that the promoter can increase metal dispersion on alumina support, hence decreasing the size of particles. The TGA analysis consistently showed four peaks which represent water removal at temperature 373-463 K, followed by decomposition of nickel nitrate to produce nickel oxide. From reaction results for Sm promotion showed glycerol conversion, XG of 27% which was 7% higher than unpromoted catalyst. The syngas productions were produced from glycerol decomposition and created H2:CO product ratio which always lower than 2.0. The H2:CO product ratio of 3 wt% Sm promoted Ni/Al2O3 catalyst was 1.70 at reaction temperature of 973 K and glycerol partial pressure of 18 kPa and suitable enough for Fischer-Tropsch synthesis.  
Unique Adsorption Properties of Malachite Green on Interlayer Space of Cu-Al and Cu-Al-SiW12O40 Layered Double Hydroxides Neza Rahayu Palapa; Novie Juleanti; Normah Normah; Tarmizi Taher; Aldes Lesbani
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.15.3.8371.653-661

Abstract

Cu-Al layered double hydroxide (LDH) was intercalated with Keggin ion of polyoxometalate           K4[a-SiW12O40] to form Cu-Al-SiW12O40 LDH. The obtained materials were analyzed by X-ray Diffraction (XRD), Fourier Transform Infra Red (FTIR) spectroscopy, and Brunaur-Emmett-Teller (BET) surface area analysis. Furthermore, the materials were used as adsorbents of malachite green from aqueous solution. Some variables for adsorption, such as: effect of adsorption times, malachite green concentration, and also adsorption temperature, were explored. The results showed that diffraction at 11.72° on Cu-Al LDH has interlayer distance of 7.56 Å. The intercalation of that LDH with [a-SiW12O40]4− ion resulted increasing interlayer distance to 12.10 Å. The surface area of material was also increased after intercalation from 46.2 m2/g to 89.02 m2/g. The adsorption of malachite green on Cu-Al and          Cu-Al-SiW12O40 LDHs followed pseudo second order kinetic and isotherm Langmuir model with adsorption capacity of Cu-Al and Cu-Al-SiW12O40 LDHs was 55.866 mg/g and 149.253 mg/g, respectively. That adsorption capacity is equal with increasing interlayer space and surface area properties of material after intercalation. Thus, the adsorption of malachite green on Cu-Al and Cu-Al-SiW12O40 LDHs is unique and dominantly occurred on interlayer space of LDH as active site adsorption. 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).
Author Guideline (2017)
Bulletin of Chemical Reaction Engineering & Catalysis 2018: BCREC Volume 13 Issue 1 Year 2018 (April 2018)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.13.1.2133.App.1-App.6

Abstract

Impeller Submergence Depth for Stirred Tanks Thiyam Thamphasana Devi; Annu Priya Sinha; Meena Thakre; Bimlesh Kumar
Bulletin of Chemical Reaction Engineering & Catalysis 2011: BCREC Volume 6 Issue 2 Year 2011 (December 2011)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.6.2.826.123-128

Abstract

Impeller submergence governs the performance of mixing tanks employed in oxygen transfer operation. Present work experimentally investigates the effect of impeller submergence depths on oxygen transfer and corresponding power consumption. It has been found that at higher range of impeller submergence, mixing tanks consume less power and gives higher values of oxygen transfer coefficient. Optimal range of submergence depth is 0.7 to 0.9 times the impeller diameter. © 2011 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)
Facile Template In-Situ Fabrication of ZnCo2O4 Nanoparticles with Highly Photocatalytic Activities under Visible-Light Irradiation Vu T. Tan; La The Vinh; Tran Ngoc Khiem; Huynh Dang Chinh
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.14.2.3613.404-412

Abstract

High specific surface area ZnCo2O4 nanoparticles were prepared via a sacrificial template accelerated hydrolysis by using nanoparticles of ZnO with highly polar properties as a template. The obtained ZnCo2O4 nanoparticles were characterized by the method of scanning electron microscopy (SEM), X-ray diffraction (XRD), Brunauer-Emmett-Teller (BET) surface area measurements, Transmission electron microscopy (TEM), Raman spectroscopy, and X-ray photoelectron spectroscopy (XPS). The obtained nanoparticles were performed as a photocatalyst for the degradation of methylene blue in aqueous solution under visible irradiation. The photocatalytic degradation rate of methylene blue onto the synthesized ZnCo2O4 was higher than that of commercial ZnO and synthesized ZnO template. 
Modification of Coal Char-loaded TiO2 by Sulfonation and Alkylsilylation to Enhance Catalytic Activity in Styrene Oxidation with Hydrogen Peroxide as Oxidant Mukhamad Nurhadi
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.12.1.501.55-61

Abstract

The modified coal char from low-rank coal by sulfonation, titanium impregnation and followed by alkyl silylation possesses high catalytic activity in styrene oxidation. The surface of coal char was undergone several steps as such: modification using concentrated sulfuric acid in the sulfonation process, impregnation of 500 mmol titanium(IV) isopropoxide and followed by alkyl silylation of n-octadecyltriclorosilane (OTS). The catalysts were characterized by X-ray diffraction (XRD), IR spectroscopy, nitrogen adsorption, and hydrophobicity. The catalytic activity of the catalysts has been examined in the liquid phase styrene oxidation by using aqueous hydrogen peroxide as oxidant. The catalytic study showed the alkyl silylation could enhance the catalytic activity of Ti-SO3H/CC-600(2.0). High catalytic activity and reusability of the o-Ti-SO3H/CC-600(2.0) were related to the modification of local environment of titanium active sites and the enhancement the hydrophobicity of catalyst particle by alkyl silylation. 
Performance of Yeast Microbial Fuel Cell Integrated with Sugarcane Bagasse Fermentation for COD Reduction and Electricity Generation Marcelinus Christwardana; J. Joelianingsih; Linda Aliffia Yoshi
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.16.3.9739.446-458

Abstract

The purpose of this analysis is to evaluate the efficiency of the Microbial Fuel Cell (MFC) system incorporated with the fermentation process, with the aim of reducing COD and generating electricity, using sugarcane bagasse extract as a substrate, in the presence and absence of sugarcane fibers. There is a possibility of turning bagasse extract into renewable bioenergy to promote the sustainability of the environment and energy. As a result, the integration of liquid fermentation (LF) with MFC has improved efficiency compared to semi-solid state fermentation (S-SSF). The maximum power generated was 14.88 mW/m2, with an average COD removal of 39.68% per cycle. The variation margin of the liquid fermentation pH readings remained slightly decrease, with a slight deflection of +0.14 occurring from 4.33. With the absence of bagasse fibers, biofilm can grow freely on the anode surface so that the transfer of electrons is fast and produces a relatively high current. Experimental data showed a positive potential after an effective integration of the LF and MFC systems in the handling of waste. The product is then simultaneously converted into electrical energy. 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). 

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