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Contact Name
Istadi
Contact Email
istadi@che.undip.ac.id
Phone
+6281316426342
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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
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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 6 Documents
Search results for , issue "2010: BCREC Volume 5 Issue 1 Year 2010 (June 2010)" : 6 Documents clear
Backmatter (Author Guideline, Copyright Transfer Agreement for Publishing Form)
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.19684

Abstract

Backmatter (Author Guideline, Copyright Transfer Agreement for Publishing Form)
Production of Biodiesel from Oleic Acid and Methanol by Reactive Distillation Kusmiyati Kusmiyati; Agung Sugiharto
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.5.1.7103.1-6

Abstract

Biodiesel is an alternative diesel fuel that is produced from vegetable oils and animal fats. Generally, it is formed by transesterification reaction of triglycerides in the vegetable oil or animal fat with an alcohol. In this work, esterification reaction was carried out using oleic acid, methanol and sulphuric acid as a catalyst by reactive distillation method. In order to determine the best conditions for biodiesel production by reactive distillation, the experiments were carried out at different temperature (100 0C, 120 0C, 150 0C and 180 0C) using methanol/oleic acid molar ratios (1:1, 5:1, 6:1, 7:1, 8:1), catalyst/ oleic acid molar ratios (0.5%wt, 1%wt, 1.5%wt and 2%wt) and reaction times (15, 30, 45, 60, 75 and 90 minutes). Results at temperature 180 0C, methanol/ oleic acid molar ratio of 8:1, amount of catalyst 1% for 90 minute reaction time gives the highest conversion of oleic acid above 0.9571. Biodiesel product from oleic acid was analysed by ASTM (American Standard for Testing Material). The results show that the biodiesel produced has the quality required to be a diesel substitute. © 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)
Hydrodynamic Studies on a Trickle Bed Reactor for Foaming Liquids Renu Gupta; Ajay Bansal
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.5.1.7127.31-37

Abstract

Hydrodynamic studies of trickle bed reactors (TBRs) are essential for the design and prediction of their performance. The hydrodynamic characteristics involving pressure drop and dynamic liquid saturation are greatly affected by the physical properties of the liquids. In the present study experiments have been carried out in a concurrent downflow air - liquid trickle bed reactor to investigate the dynamic liquid saturation and pressure drop for the water (non-foaming) and 3% polyethylene glycol and 4% polyethylene glycol foaming liquids in the gas continuous regime (GCF) and foaming pulsing regime (FP). In the GCF regime the dynamic liquid saturation was found to increase with increase in liquid flow rate for non-foaming and foaming liquids. While for 3% and 4% polyethylene glycol solutions the severe foaming was observed in the high interaction regime and the regime is referred to as foaming pulsing (FP) regime. The decrease in dynamic liquid saturation followed by a sharp rise in the pressure drop was observed during transition from gas GCF to FP regime. However in the FP regime, a dip in the dynamic liquid saturation was observed. The pressure drop for foaming liquids is observed to be manifolds higher compared to non-foaming liquid in the GCF regime.  © 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)
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)
Preparation Methods and Applications of CuO-CeO2 Catalysts: A Short Review Ram Prasad; Gaurav Rattan
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.5.1.7125.7-30

Abstract

The CuO-CeO2 catalytic systems are getting popular for catalyzing very actively the various reactions of environmental, commercial and other importance. In recent years, many methods have been in use for the preparation of versatile CuO-CeO2 catalysts. Reviewing the useful preparation methods of such catalysts is thus the need of the time in view of the globally increasing interest towards all the low temperature redox reactions. This article presents a short review on seventeen different preparation methods of the copperceria catalysts, followed by critical discussions on the related redox properties and advancements accomplished with respect to their application aspect, including a systematic compilation of the concerned newer literature in a well-concievable tabular form. © 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)
Mixed Oxide Supported MoO3 Catalyst: Preparation, Characterization and Activities in Nitration of o-xylene S. M. Kemdeo; V. S. Sapkal; G. N. Chaudhari
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.5.1.7126.39-49

Abstract

TiO2-ZrO2 mixed oxide support was prepared and impregnated with 12 wt % MoO3 and calcined at various temperatures. The resultant catalyst systems were characterized by XRD, FT-IR, BET, SEM, NH3-TPD and pyridine adsorbed FT-IR methods to know the physico-chemical changes occurred in course of thermal treatment. Activities of these catalysts were tested by employing them in the nitration of o-xylene. Mostly, 500 oC calcined catalyst sample was found to be most active for nitration reaction. Catalyst calcined at higher temperatures showed the negative influence on o-xylene conversion and 4-nitro-o-xylene selectivity. Conversion can be correlated with the presence of strong Brönsted acid sites over the catalyst surface whereas change in selectivity was found attributed to the pore diameter of the catalyst. These catalysts also performed satisfactorily, when used for nitration of other aromatics. No use of corrosive sulfuric acid and efficient reusability of the catalyst make the process environmentally friendly and economic. © 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)

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