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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 21 Documents

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Search results for , issue "2018: BCREC Volume 13 Issue 1 Year 2018 (April 2018)" : 21 Documents clear

Methyl Violet Degradation Using Photocatalytic and Photoelectrocatalytic Processes Over Graphite/PbTiO3 Composite Candra Purnawan; Sayekti Wahyuningsih; Vaishnavita Nawakusuma
Bulletin of Chemical Reaction Engineering & Catalysis 2018: BCREC Volume 13 Issue 1 Year 2018 (April 2018)
Publisher : Department of Chemical Engineering - Diponegoro University

Photocatalytic and photoelectrocatalytic degradation of methyl violet dye using Graphite/PbTiO3 composites has been conducted. The purposes of this research were to examine photocatalytic and photoelectrocatalytic degradation of methyl violet using Graphite/PbTiO3 composite. Synthesis of Graphite/PbTiO3 composite was successfully performed via sol-gel method by mixing graphite powder, titanium tetra isopropoxide precursor solution (TTIP) and Pb(NO3)2. The Graphite/PbTiO3 composites were characterized using X-Ray Diffraction (XRD), Fourier Transform-Infra Red (FT-IR), and Scanning Electron Microscopy (SEM). The XRD diffractogram and IR spectrum of Graphite/PbTiO3 composite revealed all characteristic peak of graphite and PbTiO3. Photocatalytic degradation process showed that Graphite/PbTiO3 composite with ratio 1/1 decreased concentrations of methyl violet up to 92.20 %. While photoelectrocatalytic degradation processed for 30 minutes at neutral pH and 10 V voltage degraded the methyl violet until 94 %. However, the photoelectrocatalysis is still not significance to improve methyl violet degradation compared with photocatalysis.

Cu2+ Montmorillonite K10 Clay Catalyst as a Green Catalyst for Production of Stearic Acid Methyl Ester: Optimization Using Response Surface Methodology (RSM) Enas A. Almadani; Farah W. Harun; Salina M. Radzi; Syamsul K. Muhamad
Bulletin of Chemical Reaction Engineering & Catalysis 2018: BCREC Volume 13 Issue 1 Year 2018 (April 2018)
Publisher : Department of Chemical Engineering - Diponegoro University

Clay catalyst has received much attention to replace the homogeneous catalysts in the esterification reaction to produce fatty acid methyl ester as the source of biodiesel as it is low cost, easily available, as well as environmental friendly. However, the use of unmodified clay, in particular montmorillonite K10 (MMT K10), for the esterification of fatty acids showed that the acid conversion was less than 60% and this is not preferable to the production of biodiesel. In this study, synthesis of stearic acid methyl ester using Cu2+-MMT K10 (Cu-MMT K10) was successfully optimized via response surface methodo-logy (RSM) based on 3-variable of Box-Behnken design (BB). The parameters were; reaction time (5-180 minutes), reaction temperature (80-120 oC) and concentration of Cu2+ in MMT K10 (0.25-1 M). The use of RSM in optimizing the conversion of stearic acid was successfully developed as the actual experimental conversion of stearic acid was found similar to the actual values under the optimum conditions. The model equation predicted that the following conditions would generate the maximum conversion of stearic acid (87.05 %reaction time of 62 minutes, a reaction temperature of 80 oC and catalyst used is 1.0 M Cu-MMT K10. This finding can be considered as green catalytic process as it worked at moderate reaction temperature using low cost clay catalyst with a short reaction time.

Effects of Bentonite Activation Methods on Chitosan Loading Capacity Tao Yu; Chengtun Qu; Daidi Fan; Renjun Xu
Bulletin of Chemical Reaction Engineering & Catalysis 2018: BCREC Volume 13 Issue 1 Year 2018 (April 2018)
Publisher : Department of Chemical Engineering - Diponegoro University

The adsorption capacity of bentonite clay for heavy metal removal from wastewater can be significantly enhanced by a high loading of chitosan on the surface. In order to enhance the chitosan loading, we tested activating bentonite clay by three methods prior to chitosan loading: sulfuric acid, calcination, and microwave treatments. Meanwhile, several parameters during chitosan loading, namely the initial chitosan concentration, stirring speed, reaction time, temperature, and pH value were investigated. Our results indicate that chitosan is attached to bentonite clay through intercalation and surface adsorption according to X-ray Diffraction (XRD), Scanning Eelectron Microscopy (SEM), and Fourier Transform Infrared Spectroscopy (FTIR) analyses. The maximum chitosan loading on 200-mesh raw bentonite clay (126.30 mg/L) was achieved under the following conditions: the initial chitosan concentration of 1000 mg/L, the stirring speed of 200 rpm, pH of 4.9, 60 min of reaction time, and temperature of 30 °C. The chitosan loading was further increased to 256.30, 233.70, and 208.83 mg/g, when using bentonite clay activated through 6 min of microwave irradiation (800 W), 10 % sulfuric acid treatment, and calcinations at 600 °C, respectively. When the chitosan loading was increased from 34.76 to 233.7 mg/g, the removal percentages of Cu(II), Cr(VI), and Pb(II) were improved, respectively from 78.90 to 95.5 %, from 82.22 to 98.74 %, from 60.09 to 86.18 %.

Enhanced Photocatalytic Activity of La3+ doped Bicrystalline Titania Prepared via Combustion method for the Degradation of Cationic dye Under Solar Illumination Radhika R Nair; Mothi Krishna Mohan; Sunaja Devi
Bulletin of Chemical Reaction Engineering & Catalysis 2018: BCREC Volume 13 Issue 1 Year 2018 (April 2018)
Publisher : Department of Chemical Engineering - Diponegoro University

La3+ doped TiO2 photocatalysts were successfully synthesized by combustion method in the presence of urea and were characterized by various physico-chemical techniques. Further, the photocatalytic performance of the synthesized catalysts was monitored by photocatalytic degradation of synthetic cationic dye-Methylene Blue (MB) under solar illumination. The bicrystalline phase of anatase and rutile was confirmed by X-ray diffraction analysis. Moreover, the transformation from anatase to rutile phase proceeds at a slower rate in the La3+ doped TiO2 catalysts. Effective separation of charge carriers, a synergistic effect in the bicrystalline framework of anatase and rutile, smaller crystallite size, and higher concentration of surface adsorbed hydroxyl groups helped these catalysts to show improved activity for the dye degradation.

Simultaneous Control of NOx-Soot by Substitutions of Ag and K on Perovskite (LaMnO3) Catalyst Ganesh Chandra Dhal; Subhashish Dey; Devendra Mohan; Ram Prasad
Bulletin of Chemical Reaction Engineering & Catalysis 2018: BCREC Volume 13 Issue 1 Year 2018 (April 2018)
Publisher : Department of Chemical Engineering - Diponegoro University

The different Ag and K substituted perovskite catalysts including base catalyst were LaMnO3 by the solid state method and the diesel soot was prepared in the laboratory. Their structures and physico-chemical properties were characterized by X-ray diffraction (XRD), BET, SEM, H2-TPR, and XPS techniques. The Ag Substituted at A-site perovskite structured catalysts are more active than other type of catalysts for the simultaneous soot-NOX reaction, When Ag and K are simultaneously introduced into LaMnO3 catalyst, soot combustion is largely accelerated, with the temperature (Tm) for maximal soot conversion lowered by at least 50 °C, moreover, NOX reduction by soot is also facilitated. The high activity of La0.65Ag0.35MnO3 perovskite catalyst is attributed to presence of metallic silver in the catalyst. The activity order of Ag doped LaMnO3 is as follows La0.65Ag0.35MnO3 > La0.65Ag0.2MnO3 > La0.65Ag0.4MnO3 > La0.65Ag0.1MnO3. The dual substitution of silver and potassium in place of La in LaMnO3 gives better activity than only silver doped catalyst. In a series of La0.65AgxK1-xMnO3, the optimum substitution amount of K is for x=0.25. The single and doubled substituted perovskite catalyst proved to be effective in the simultaneous removal of NOX and soot particulate, the two prevalent pollutants in diesel exhaust gases in the temperature range 350-480 °C.

Lignin-containing Feedstock Hydrogenolysis for Biofuel Component Production Elena Shimanskaya; Аntonina A. Stepacheva; Esther Sulman; Evgeny Rebrov; Valentina Matveeva
Bulletin of Chemical Reaction Engineering & Catalysis 2018: BCREC Volume 13 Issue 1 Year 2018 (April 2018)
Publisher : Department of Chemical Engineering - Diponegoro University

In this paper, the commercial 5%Pd/C and 5%Pt/C catalysts and synthesized 5%Pt/MN-270 and 5%Pd/MN-270 were used in the hydrogenolysis of lignocellulosic material (softwood sawdust) to obtain liquid fuels in the form of hydrocarbons. As lignin has a very complex structure, anisole was used as a model compound. It was found that the use Pt-containing catalysts based on hypercrosslinked polystyrene in both processes of anisole and lignin-containing feedstock conversion allowed obtaining the highest yield of oxygen-free hydrocarbons (up to 96 wt. %). Besides, the polymer based catalysts showed high stability in hydrogenolysis process in comparison with the commercial carbon based catalysts.

Negative Effect of Calcination to Catalytic Performance of Coal Char-loaded TiO2 Catalyst in Styrene Oxidation with Hydrogen Peroxide as Oxidant Mukhamad Nurhadi; Ratna Kusumawardani; Hadi Nur
Bulletin of Chemical Reaction Engineering & Catalysis 2018: BCREC Volume 13 Issue 1 Year 2018 (April 2018)
Publisher : Department of Chemical Engineering - Diponegoro University

The research of negative effect of calcination to catalytic performance of coal char-loaded TiO2 catalyst in styrene oxidation with hydrogen peroxide as oxidant has successfully done. The effects of calcination step to catalyst properties were characterized with Fourier Transform Infra Red (FTIR), X-ray Difraction (XRD), nitrogen adsorption, Field Emission Scanning Electron Microscopy (FESEM), and Transmission electron microscopy (TEM). The catalytic performance of the catalysts has been investigated in styrene oxidation with hydrogen peroxide as oxidant. The catalytic study showed the calcination step influenced to catalytic properties and could decrease the catalytic performance of coal char-loaded TiO2 catalyst in styrene oxidation.

Catalytic Properties of Alumina-Supported Ruthenium, Platinum, and Cobalt Nanoparticles towards the Oxidation of Cyclohexane to Cyclohexanol and Cyclohexanone Ilhem Rekkab-Hammoumraoui; Abderrahim Choukchou-Braham
Bulletin of Chemical Reaction Engineering & Catalysis 2018: BCREC Volume 13 Issue 1 Year 2018 (April 2018)
Publisher : Department of Chemical Engineering - Diponegoro University

A series of metal-loaded (Ru, Pt, Co) alumina catalysts were evaluated for the catalytic oxidation of cyclohexane using tertbutylhydroperoxide (TBHP) as oxidant and acetonitrile or acetic acid as solvent. These materials were prepared by the impregnation method and then characterized by Inductively Coupled Plasma-Optical Emission Spectroscopy (ICP-OES), H2 chemisorption, Fourier Transformed Infrared Spectroscopy (FTIR), High-Resolution Transmission Electron Microscopy (HRTEM), and X-ray Diffraction (XRD). All the prepared materials acted as efficient catalysts. Among them, Ru/Al2O3 was found to have the best catalytic activity with enhanced cyclohexane conversion of 36 %, selectivity to cyclohexanol and cyclohexanone of 96 % (57.6 mmol), and cyclohexane turnover frequency (TOF) of 288 h-1.

A Computational Fluid Dynamics Study of Turbulence, Radiation, and Combustion Models for Natural Gas Combustion Burner Yik Siang Pang; Woon Phui Law; Kang Qin Pung; Jolius Gimbun
Bulletin of Chemical Reaction Engineering & Catalysis 2018: BCREC Volume 13 Issue 1 Year 2018 (April 2018)
Publisher : Department of Chemical Engineering - Diponegoro University

This paper presents a Computational Fluid Dynamics (CFD) study of a natural gas combustion burner focusing on the effect of combustion, thermal radiation and turbulence models on the temperature and chemical species concentration fields. The combustion was modelled using the finite rate/eddy dissipation (FR/EDM) and partially premixed flame models. Detailed chemistry kinetics CHEMKIN GRI-MECH 3.0 consisting of 325 reactions was employed to model the methane combustion. Discrete ordinates (DO) and spherical harmonics (P1) model were employed to predict the thermal radiation. The gas absorption coefficient dependence on the wavelength is resolved by the weighted-sum-of-gray-gases model (WSGGM). Turbulence flow was simulated using Reynolds-averaged Navier-Stokes (RANS) based models. The findings showed that a combination of partially premixed flame, P1 and standard k-ε (SKE) gave the most accurate prediction with an average deviation of around 7.8% of combustion temperature and 15.5% for reactant composition (methane and oxygen). The results show the multi-step chemistry in the partially premixed model is more accurate than the two-step FR/EDM. Meanwhile, inclusion of thermal radiation has a minor effect on the heat transfer and species concentration. SKE turbulence model yielded better prediction compared to the realizable k-ε (RKE) and renormalized k-ε (RNG). The CFD simulation presented in this work may serve as a useful tool to evaluate a performance of a natural gas combustor.

Comparison of Five Advanced Oxidation Processes for Degradation of Pesticide in Aqueous Solution Augustine Chioma Affam; Malay Chaudhuri; Shamsul Rahman M. Kutty
Bulletin of Chemical Reaction Engineering & Catalysis 2018: BCREC Volume 13 Issue 1 Year 2018 (April 2018)
Publisher : Department of Chemical Engineering - Diponegoro University

The study compared the technical efficiency and economic cost of five advanced oxidation processes (Fenton, UV photo-Fenton, solar photo-Fenton, UV/TiO2/H2O2 and FeGAC/H2O2) for degradation of the pesticides chlorpyrifos cypermethrin and chlorothalonil in aqueous solution. The highest degradation in terms of COD and TOC removals and improvement of the biodegradability (BOD5/COD ratio) index (BI) were observed to be (i) Fenton - 69.03% (COD), 55.61% (TOC), and 0.35 (BI); (ii) UV photo-Fenton -78.56% (COD), 63.76% (TOC) and 0.38 (BI); (iii) solar photo-Fenton - 74.19% (COD), 58.32% (TOC) and 0.36 (BI); (iv) UV/TiO2/H2O2 - 53.62% (COD), 21.54% (TOC), and 0.26 (BI); and (v) the most technical efficient and cost effective process was FeGAC/H2O2. At an optimum condition (FeGAC 5 g/L, H2O2 100 mg/L, and reaction time of 60 min at pH 3), the COD and TOC removal efficiency were 96.19 and 85.60%, respectively, and the biodegradation index was 0.40. The degradation rate constant and cost were 0.0246 min-1 and $0.74/kg TOC, respectively. The FeGAC/H2O2 process is the most technically efficient and cost effective for pretreatment of the pesticide wastewater before biological treatment.

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