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Bulletin of Chemical Reaction Engineering & Catalysis

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Published by Universitas Diponegoro

ISSN : - EISSN : 19782993 DOI : -

Core Subject : Science, Engineering,

Chemical Engineering, Chemistry & Bioengineering Chemistry

Bulletin of Chemical Reaction Engineering & Catalysis (e-ISSN: 1978-2993), an international journal, provides a forum for publishing the novel technologies related to the catalyst, catalysis, chemical reactor, kinetics studies, and chemical reaction engineering.

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Articles 524 Documents

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Kinetic Modeling of Flocculation and Coalescence in the System Emulsion of Water-Xylene-Terbutyl Oleyl Glycosides Harsa Pawignya; Tutuk Djoko Kusworo; Bambang Pramudono
Bulletin of Chemical Reaction Engineering & Catalysis 2019: BCREC Volume 14 Issue 1 Year 2019 (April 2019)
Publisher : Department of Chemical Engineering - Diponegoro University

The development of a mathematical model for explaining the kinetics of flocculation and coalescence of emulsion droplets is essential to study the stability of an emulsion system of the kinetics of emulsion stability. Mathematic models was developed from the equation Van Den Tempel by modifying emulsion systems. The emulsion was made by mixing water-xylene and surfactant tert-butyl oleyl glycosides. This research studied the effect of stirrer speed on the value of flocculation rate constant (a) and coalescence rate constant (K). The model identified the emulsion development condition whether controlled by coalescence or flocculation. It was observed that under lower agitation speed (1000 rpm) the emulsion development was controlled by flocculation mechanism, while a faster agitation (2000 rpm or higher) exhibited coalescence controlled mechanism. The results confirmed that the 1st model was the most appropriate for water-xylene-TBOG emulsion system. From four models after fitting with experimental data, the most suitable model is 4th model, because it has the smallest error of 2.22 %.

Mesoporous Co3O4 as a New Catalyst for Allylic Oxidation of Cyclohexene Hajer Azzi; I. Rekkab-Hammoumraoui; L. Chérif-Aouali; A. Choukchou-Braham
Bulletin of Chemical Reaction Engineering & Catalysis 2019: BCREC Volume 14 Issue 1 Year 2019 (April 2019)
Publisher : Department of Chemical Engineering - Diponegoro University

Mesoporous cobalt oxide was investigated for the liquid phase oxidation of cyclohexene using tertiobutylhydroperoxide (TBHP) as an oxidant. The results were compared with several series of supported cobalt catalysts to study the influence of the cobalt loading and solvents on the overall conversion and selectivity. Mesoporous cobalt was synthesized through the nanocasting route using siliceous SBA-15 mesoporous material as a hard template and cobalt nitrate as the cobalt oxide precursor. Supported cobalt oxide catalysts (Co/MxOy) were synthesized by the impregnation method using two loadings (1 and 5 wt.%) and Al2O3, TiO2, and ZrO2 as supports. Samples were characterised by means: elemental analysis, X-ray powder Diffraction (XRD), BET (surface area), UV-Vis DR Spectroscopy, and MET. The results obtained showed that the cobalt oxide retains the mesoporous structure of SBA-15, and in all Co/MxOy, crystalline Co3O4 and CoO phases are observed. The mesoporous cobalt oxide is more active than the supported cobalt catalysts in the allylic oxidation of cyclohexene, with a conversion of 78 % of cyclohexene and 43.3 % selectivity toward 2-cyclohexene-1-ol. The highest activity of mesoporous cobalt oxide could be ascribed to its largest surface area. Furthermore, Co3O4 has both Lewis and Brönsted acidic sites whereas Co/MxOy has only Lewis acidic sites, which could also explain its superior catalytic activity. Moreover, mesoporous cobalt oxide was more stable than supported cobalt catalysts. Therefore, this catalyst is promising for allylic oxidation of alkenes.

PEGylated MoS2 Nanosheets: A Dual Functional Photocatalyst for Photodegradation of Organic Dyes and Photoreduction of Chromium from Aqueous Solution Madima Ntakadzeni; William Wilson Anku; Neeraj Kumar; Penny Poomani Govender; Leelakrishna Reddy
Bulletin of Chemical Reaction Engineering & Catalysis 2019: BCREC Volume 14 Issue 1 Year 2019 (April 2019)
Publisher : Department of Chemical Engineering - Diponegoro University

This article reports the synthesis of PEGylated microspheres of MoS2 nanosheets through the hydrothermal method and its application in rhodamine B and methylene blue dyes photodegradation, and photoreduction of chromium(VI) to chromium(III) in water under illumination with visible light. The catalyst was characterized using X-ray Diffraction (XRD), Transmission Electron Microscopy (TEM), Field Emission Scanning Electron Microscopy (FESEM), Energy Dispersive X-ray Spectroscopy (EDS), Fourier Transform Infra Red (FTIR), Thermo-gravimetric Analysis (TGA), and UV-Vis spectroscopies. XRD result reveals the MoS2 nanosheets to be present in the hexagonal phase of MoS2. SEM, TEM, and HRTEM images show that the synthesised sample has spherical shapes made up of several thin sheets of MoS2. The catalyst showed visible light responsivity with a calculated band gap of 1.92 eV. The MoS2 nanosheets exhibited high degradation efficiency against both dyes. The RhB and MB dyes experienced degradation efficiencies of 97.30 % (RhB) and 98.05 % (MB) in 75 min 90 min, respectively. The MoS2 photocatalyst is also observed to be effective in photocatalytic reduction of Cr(VI) and displayed 91.05% reduction of Cr(VI) to Cr(III) in 75 min. The results reveal that the synthesised MoS2 nanosheet is a good photocatalytic material for degradation of dyes and reduction of Cr(VI) to Cr(III) in water.

Development of CaO/PVA Catalyst from Fish Bone for Biodiesel Production Sarina Sulaiman; Nor Fatin Abdul Jamaludin; Nassereldeen Ahmed Kabbashi
Bulletin of Chemical Reaction Engineering & Catalysis 2019: BCREC Volume 14 Issue 1 Year 2019 (April 2019)
Publisher : Department of Chemical Engineering - Diponegoro University

In this study, calcium oxide were synthesized from fish bone waste and the optimum condition : catalyst amount, temperature and methanol to oil ratio (molar) for biodiesel production were studied. The calcium oxide (CaO) derived from fish bone wastes was then supported on polyvinyl alcohol (PVA) to easily separate the catalyst and biodiesel. Fish bone were dried in oven at 70 oC for 24 hr before calcination process at 900 oC for 4 hours. The biodiesel yield was studied by varying three parameters, namely methanol to oil ratio (molar) (6:1 - 20:1), amount of catalyst (1-10 wt%) and temperature (55-65 oC). The highest yield obtained from this study was at 80.40 % with catalyst amount of 10 wt%, methanol to oil ratio (molar) of 20:1 and temperature of 65 oC.

Microwave-Assisted Synthesis of DUT-52 and Investigation of Its Photoluminescent Properties Ruth Febriana Kesuma; Aep Patah; Yessi Permana
Bulletin of Chemical Reaction Engineering & Catalysis 2019: BCREC Volume 14 Issue 1 Year 2019 (April 2019)
Publisher : Department of Chemical Engineering - Diponegoro University

A zirconium metal-organic framework (MOF) of DUT-52 (DUT: Dresden University of Technology) was synthesized herein by reacting zirconium tetrachloride (ZrCl4) and 2,6-naphthalenedicarboxylic acid (H2NDC) in DMF under microwave heating at 115 oC for 25 min. This synthetic procedure was more efficient than a solvothermal method, by which a long thermal exposure (24 h) of 100-150 oC was required to produce the same MOF. The MOF has a thermal stability of 560 °C, prior to partial loss of interconnected 2,6-naphthalenedicarboxylate (NDC) linkers at some structure building units (SBU). Crystallinity of this DUT-52 was ca. 77 %, which was the same as one synthesized solvothermally. Diffuse Reflectance UV-Vis spectra revealed an absorption at λex of 287 nm, which was equivalent to a bandgap energy of 4.32 eV. Electron excitations of this DUT-52 at 275 and 300 nm gave emission wavelength of 433 nm (a purple region), indicating a prospective use of DUT-52 as a photoluminescent material.

Algerian Acid Activated Clays as Efficient Catalysts for a Green Synthesis of Solketal by Chemoselective Acetalization of Glycerol with Acetone Kouider Alali; Fouad Lebsir; Sondes Amri; Ali Rahmouni; Ezzedine Srasra; Néji Besbes
Bulletin of Chemical Reaction Engineering & Catalysis 2019: BCREC Volume 14 Issue 1 Year 2019 (April 2019)
Publisher : Department of Chemical Engineering - Diponegoro University

The production of solketal and conversion of glycerol takes a major importance in the field of the sustainability of the biodiesel industry. The synthesis of (2,2-dimethyl-1,3-dioxolan-4-yl)methanol by the acetalization of glycerol with acetone successfully applied out using various Algerian acid activated clays (maghnia-H+) under autogenous pressure and without solvent. The acid catalyst clays are prepared by an easy technique by activation with the available and low-cost Maghnia clay. The purified Maghnia clay named ALC and the resulting series of acid-activated clays AL1, AL2, AL3, and AL4 are characterized by X-ray Fluorescence (XRF) investigation, N2-adorption/desorption Brunauer–Emmett–Teller (BET) surface area, X-rays Diffraction (XRD), Fourier Transform Infra Red (FT-IR) spectroscopy, SEM microscopy and the cation exchange capacity (CEC) with copper bisethylenediamine complex method, in order to study the effect of activation at the acid and the catalytic behaviour in the acetalization reaction. The results show a high catalytic activity whose that the yield of solketal production interest reached 95 % at a temperature of 40 °C for a reaction time of 48 hours with full selectivity and glycerol conversion reaching up to 89 %. A mechanistic is proposed to explain the chemoselective of solketal production. These results indicate the potential of this Algerian acid activated clays catalysts for the acetalization of glycerol for an environmentally benign process.

Studies on H2-Assisted Liquefied Petroleum Gas Reduction of NO over Ag/Al2O3 Catalyst Pratichi Singh; Deepak Yadav; Pooja Thakur; Jitendra Pandey; Ram Prasad
Bulletin of Chemical Reaction Engineering & Catalysis 2018: BCREC Volume 13 Issue 2 Year 2018 (August 2018)
Publisher : Department of Chemical Engineering - Diponegoro University

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.13.2.1307.227-235

Hydrocarbon-Selective catalytic reduction (HC-SCR) is one of the potential methods to remove NOx emissions from diesel engine, lean burn petrol engines and natural gas engines exhaust. Ag/Al2O3 is a good catalyst for HC-SCR of NOx under lean-burn conditions. Further, addition of small amount of H2 is effective for enhancing HC-SCR activity. This effect is unique to silver and to specific Ag/support combinations, namely, Ag/γ-Al2O3. Various HC reductants, such as: octane, decane, dodecane and propane, have been reported in the literatures. Only a single study on LPG as a reductant over Cu-ZSM catalyst was reported. There was no work reported on H2 assisted LPG over Ag/Al2O3 catalyst. Thus, this gap in the literature is filled with the present investigation of NO reduction over 2 wt.% Ag/Al2O3 catalyst using LPG reductant. The fresh and used catalyst was characterized by various techniques like low temperature N2-adsorption, XRD, XPS and SEM. There was practically no change in the characteristics of the fresh and used catalyst. Two different reductants of CO and LPG were compared for SCR of NO over the catalyst without and with H2-assisted. The experiments were performed in a fixed bed tubular flow reactor under the following conditions: 100mg catalyst; 0.13% NO, 2.5% LPG/CO, 1% H2, 10% O2, rest Ar; total flow rate 60 mL/min; temperature ambient 400 oC and pressure 1 atm. Around 100% conversion of NO was achieved using LPG reductant. Light off temperature of NO reduction significantly reduced by H2assisted LPG reductant. The maximum conversion of NO with CO was limited to 35.15% at temperature of 224 oC and above. Whereas, 97.79 % NO conversion was achieved at 365 oC with LPG reductant. While, the maximum conversions with H2-LPG and H2-CO reductants were 100 and 99.46% at 117 and 220 oC, respectively. Therefore, H2-LPG-SCR of NOx over 2 wt.% Ag/Al2O3 catalyst system can be used to get 100% reduction at low temperature.

The Impact of Hydrogen Peroxide as An Oxidant for Solvent-free Liquid Phase Oxidation of Benzyl Alcohol using Au-Pd Supported Carbon and Titanium Catalysts Sarhan Sanaa Tareq; Mohd. Izham Saiman; Taufiq-Yap Yun Hin; Abdul Halim Abdullah; Umer Rashid
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.13.2.1204.373-385

The solvent free oxidation of benzyl alcohol was conducted employing Au and Pd supported catalysts, while utilizing hydrogen peroxide 35% (H2O2) as the oxidant, H2O2 is very cheap, mild, and an environment friendly reagent, which produced water as the only by-product. Various proportions of Au-Pd catalysts on carbon and titanium oxide activated as supports were synthesized through the use of sol immobilization catalyst synthesis technique. Characterization of the synthesized catalysts was performed using X-Ray Diffraction (XRD), Brunauer-Emmett-Teller (BET), Field Emission Scanning Electron Microscopy (FESEM), and Transmission Electron Microscopy (TEM). It was found that the synthesized Au-Pd/ activated carbon catalyst was beneficial for the solvent free oxidation of benzyl alcohol after its containing high surface area measuring 871 m2g-1. Analysis of the TEM data and particle dimension revealed smaller and narrower particle size of 1 wt%. Thus, the distribution of Au-Pd/C was attained. Carbon-supported bimetallic catalysts presented a higher conversion compared to catalysts that are supported titanium oxide (TiO2) for for the oxidation reaction of benzyl alcohol. It was determined that this technique was a suitable process for catalyst synthesis with high selectivity, same distribution of the particle size and activations.

Cu/Pd Bimetallic Supported on Mesoporous TiO2 for Suzuki Coupling Reaction Mothi Krishna Mohan; K. R. Sunajadevi; Nobi K Daniel; Soumya Gopi; Sugunan Sugunan; Nikhil Chandra Perumparakunnel
Bulletin of Chemical Reaction Engineering & Catalysis 2018: BCREC Volume 13 Issue 2 Year 2018 (August 2018)
Publisher : Department of Chemical Engineering - Diponegoro University

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.13.2.1393.286-294

Generally bimetallic catalysts are more superior to monometallic catalysts and provide a better platform for the development of novel catalysts with enhanced activity, selectivity, and stability. In the current work we have prepared Cu/Pd bimetallic supported on mesoporous TiO2 by hydrothermal method. The prepared system was characterized by various physico-chemical techniques such as XRD, TG-DTG, SEM, EDAX, BJH isotherm, and XPS. Thermal stability and complete electronic structure were identified from TG and XPS measurements respectively. The bimetallic system was found to be very active in Suzuki cross-coupling reaction using different substrates. The products were separated and purified by column chromatography and the resultant products were characterized thoroughly by 1H NMR, and FT-IR analysis.

Triglycerides Hydrocracking Reaction of Nyamplung Oil with Non-sulfided CoMo/γ-Al2O3 Catalysts Rismawati Rasyid; Rahmaniah Malik; Heri Septya Kusuma; Achmad Roesyadi; Mahfud Mahfud
Bulletin of Chemical Reaction Engineering & Catalysis 2018: BCREC Volume 13 Issue 2 Year 2018 (August 2018)
Publisher : Department of Chemical Engineering - Diponegoro University

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.13.2.734.196-203

The purpose of this research are to study the temperature influence in hydrocracking process of the nyamplung oil (Calophyllum inophyllum) using a non-sulfided CoMo/γ-Al2O3 catalyst and to develop a simple kinetic model in interpreting the data of hydrocracking products. The experiment was carried out in a pressurized batch reactor operated pressure up 30 bar. The CoMo catalyst supported with γ-Al2O3 was prepared through impregnation method without sulfidation process. The operating temperature varied from 200 to 350 oC. The results show that the non-sulfided CoMo/γ-Al2O3 catalysts, nyamplung oil triglycerides can converted into gasoil and gasoline-like hydrocarbons. The triglyceride hydrocracking reaction of nyamplung oil followed a several stages, i.e., hydrogenation, dehydrogenation, and cracking. Based on the compounds contained in liquid product, hydrocracking reaction was dominated by decarboxylation. The products obtained in hydrocracking process of nyamplung oil are classified to gasoil (C11-C18) and gasoline (C5-C10). The triglycerides hydrocracking reaction of nyamplung oil was assumed by following a series reaction mechanism and a simple kinetic model used for determined the kinetics constants. The highest reaction conversion is 99.10% obtained at temperature of 350 °C for 160 minutes reaction time.

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