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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 21 Documents
Search results for , issue "2022: BCREC Volume 17 Issue 2 Year 2022 (June 2022)" : 21 Documents clear
Effect of Polymer Concentration on the Photocatalytic Membrane Performance of PAN/TiO2/CNT Nanofiber for Methylene Blue Removal through Cross-Flow Membrane Reactor Lathifah Puji Hastuti; Ahmad Kusumaatmaja; Adi Darmawan; Indriana Kartini
Bulletin of Chemical Reaction Engineering & Catalysis 2022: BCREC Volume 17 Issue 2 Year 2022 (June 2022)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.17.2.13668.350-362

Abstract

A photocatalytic membrane combining photocatalyst and membrane technology based on polyacrylonitrile (PAN) and TiO2/CNT has been developed. Such combination is to overcome fouling formation on the membrane, thus prolonging the membrane lifetime and enhancing the efficiency on the waste treatment. PAN nanofiber was prepared by electrospinning method. The precursor solution was dissolved PAN and dispersed TiO2/CNT in N,N-Dimethylformamide (DMF). PAN concentration in the precursor solution was varied at 4.5, 5.5, 6.5, 7.5, and 8.5%. The effect of PAN concentration on the fiber morphology and pore size was discussed. The performance of the resulted membrane on methylene blue (MB) removal was also investigated on a cross-flow system. SEM images of the resulted membrane identified that PAN nanofiber was successfully fabricated with random orientation. The PAN 6.5% showed the highest diffraction intensity of the anatase crystalline phase of TiO2. The additions of CNT and TiO2 lead to the formation of a cluster of beads as confirmed by TEM. Increasing the concentration of PAN increased the fiber diameter from 206 to 506 nm, slightly decreased the surface area and pore size, respectively, from 32.739 to 21.077 m2.g−1 and from 6.38 to 4.75 nm. The PAN/TiO2/CNT nanofibers show type IV of the adsorption-desorption N2 isotherms with the H1 hysteresis loops. Membrane PAN/TiO2/CNT at PAN concentration of 6.5% shows the optimum performance on the MB color removal by maintaining the percentage of rejection (%R) at 90% for 240 min and permeability of 750 LMH. 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). 
Photocatalytic Degradation of Polyethylene Microplastics and Disinfection of E. coli in Water over Fe- and Ag-Modified TiO2 Nanotubes Yuwendi Yuwendi; Muhammad Ibadurrohman; Setiadi Setiadi; Slamet Slamet
Bulletin of Chemical Reaction Engineering & Catalysis 2022: BCREC Volume 17 Issue 2 Year 2022 (June 2022)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.17.2.13400.263-277

Abstract

In this study, Fe- and Ag-modified TiO2 nanotubes were synthesized via an anodization method as photocatalysts for degradation of polyethylene microplastics and disinfection of Escherichia coli (E. coli). The anodization voltage, as well as the Fe3+ or Ag+ concentrations on TiO2 nanotubes were evaluated and correlated to their corresponding photocatalytic properties. TiO2 nanotubes were firstly synthesized by anodization of Ti plates in a glycerol-based electrolyte, followed by incorporation of either Fe or Ag via a Successive Ionic Layer Adsorption and Reaction (SILAR) method with Fe(NO3)3 and AgNO3 as Fe and Ag precursors, respectively. UV-Vis DRS shows that the addition of Fe or Ag on TiO2 nanotubes causes a redshift in the absorption spectra. The X-ray diffractograms indicate that, in the case of Fe-modified samples, Fe3+ was successfully incorporated into TiO2 lattice, while Ag scatters around the surface of the tubes as Ag and Ag2O nanoparticles. A microplastic degradation test was carried out for 90 mins inside a photoreactor with UVC illumination. TiO2 nanotubes that are anodized with a voltage of 30 V exhibit the best degradation results with 17.33% microplastic weight loss in 90 mins. Among the modified TiO2 nanotubes, 0.03 M Ag-TiO2 was the only one that surpassed the unmodified TiO2 in terms of microplastic degradation in the water, offering up to 18% microplastic weight loss in 90 min. In terms of E. coli disinfection, 0.03M Ag-TiO2 exhibit better performance than its unmodified counterpart, revealing 99.999% bactericidal activities in 10 mins. 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). 
Nanocomposite ZnO/g-C3N4 for Improved Degradation of Dyes under Visible Light: Facile Preparation, Characterization, and Performance Investigations Tu Anh Nguyen Thi; Anh- Tuan Vu
Bulletin of Chemical Reaction Engineering & Catalysis 2022: BCREC Volume 17 Issue 2 Year 2022 (June 2022)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.17.2.13931.403-419

Abstract

In this study, ZnO/g-C3N4 nanocomposites were prepared via a physical mixing-calcination process for improved degradation of dyes under visible light irradiation. The BET surface area, pore volume, crystal size, and pHpzc of the ZnO/g-C3N4 composite were 3.9 m2/g, 0.034 cm3/g, 18.1 nm, and 7.7, respectively. Although the morphology of the ZnO/g-C3N4 composite was very different from that of pure g-C3N4, their average pore sizes were similar. The Eg of the ZnO/g-C3N4 composite (3.195 eV) was slightly lower than that of ZnO (3.195) but much higher than that of g-C3N4 (2.875). The interface interaction of ZnO and g-C3N4, which was revealed by oscillations of Zn-C, benefited the transport of photoinduced charge carriers and reduced the recombination of electron-hole. As the result, the ZnO/g-C3N4 composite had higher photocatalytic activity than ZnO and g-C3N4. Its degradation efficiency (DE) value for methylene blue (MB) in 90 min and rate constant were 93.2 % and 0.025 min‑1, respectively. In addition, the effects of ZnO/urea molar ratio, catalyst dosage, solution pH, and concentration of dye on photocatalytic degradation of MB were completely investigated. The photocatalytic performance of the ZnO/g-C3N4 composite was evaluated by the degradation of other persistent organic compounds, also compared to other catalysts in the literatures. 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). 
Numerical Study of a Water Gas Shift Fixed Bed Reactor Operating at Low Pressures Wail El-Bazi; Mustapha Bideq; Abderrahim El-Abidi; Said Yadir; Bajil Ouartassi
Bulletin of Chemical Reaction Engineering & Catalysis 2022: BCREC Volume 17 Issue 2 Year 2022 (June 2022)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.17.2.13510.304-321

Abstract

Today, hydrogen has become one of the most promising clean energy. Several processes allow obtaining hydrogen, among them there is the Water Gas Shift (WGS) reaction. On an industrial scale, WGS reaction takes place at high pressure [25–35 bar]. At high pressure, the cost of the process rises due to the energy consumed by compression, and the reduction in the lifetime of the equipment and the catalyst. At low pressures, catalyst lifetime can reach many years and the energy cost is reduced. It is for this reason that we are interested in modelling and simulation of a WGS converter operating at low pressures close to atmospheric pressure. In this work, a numerical study was conducted in order to determine the conditions allowing good rector operating at low pressure. A number of drawbacks of the process were identified. These drawbacks are essentially the non-negligible pressure drops and the strong intraparticle diffusion resistances. The prediction of the concentrations and the reaction rate within the pellet showed that the active zone of the pellet is located near the particle surface. It has also been shown that the resistances to interfacial mass and heat transfer are insignificant. The study of pressure effect showed that the pressure increase reduces the required catalyst mass to achieve equilibrium. Finally, this work revealed that the decrease in temperature and the increase in the concentrations of the reactants by increasing their fluxes, make it possible to increase the effectiveness factor of the catalyst and the conversion of carbon monoxide. 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 Crude Palm Oil over Bimetallic Oxide NiO-CdO/biochar Catalyst Allwar Allwar; Rina Maulina; Tatang Shabur Julianto; Annisa Ayu Widyaningtyas
Bulletin of Chemical Reaction Engineering & Catalysis 2022: BCREC Volume 17 Issue 2 Year 2022 (June 2022)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.17.2.14074.476-485

Abstract

The bimetallic oxide NiO-CdO/biochar catalyst was prepared by coprecipitation and calcination methods. Characterizations of catalyst were carried out using Fourier Transform Infra Red (FTIR), Surface Area Analyzer (SAA), X-ray Diffraction (XRD), and Scanning Electron Microscope-Energy Dispersive X-ray (SEM-EDX) mapping methods. The catalyst showed a good average crystalized size of 12.30 nm related to the nanoparticles and high dispersion of Ni and Cd metals  on the biochar surface. Analysis of liquid fuel products was observed using Gas Chromatography - Mass Spectrometry (GC-MS) which was separated to the main product of gasoline fraction (C6–C10), and the second product of kerosene fraction (C11–C16), and diesel fraction (C17–C23). The presence of the catalyst in the hydrocracking resulted in more liquid product of 56.55 wt% than the thermal cracking with a liquid product of 20.55 wt%. The best performance activity of catalyst was found at a temperature of 150 °C with high selectivity to hydrocarbon fuel with 12 types of gasoline fractions (39.24 wt%) compared to gasoline fractions obtained at higher hydrocracking temperatures of 250 °C and 350 °C. The results of this study showed that the bimetallic oxide catalyst supported with biochar from palm kernel shell plays an important role in the hydrocracking process to increase the selectivity of the gasoline fraction. 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). 
The Effect of Zinc Oxide Supported on Gelatin Mesoporous Silica (GSBA-15) on Structural Character and Their Methylene Blue Photodegradation Performance Maria Ulfa; Ida Setiarini
Bulletin of Chemical Reaction Engineering & Catalysis 2022: BCREC Volume 17 Issue 2 Year 2022 (June 2022)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.17.2.13712.363-374

Abstract

Gelatin mesoporous silica SBA-15 (GSBA-15) with rod-like morphology has been successfully synthesized by hydrothermal method using P-123:gelatin, then aged at 90 °C for 24 h and calcined at 550 °C for 5 h. GSBA-15 was impregnated with ZnO amounts of 1; 5; and 10 wt% to obtain Zn/GSBA-15. Samples were characterized by X-ray Diffraction (XRD), Fourier Transform Infra Red (FTIR), Scanning Electron Microscopy (SEM), and Brunauer-Emmett-Teller (BET). The efficiency of methylene blue photodegradation was determined by a UV-Vis spectrophotometer. The FTIR result is functional groups of ZnO/GSBA-15, those were Si−O−Si, −OH, Zn−OH, and Zn−O. The morphology of ZnO/GSBA-15 was rod-like, and it consisted of silica, oxygen, and Zn. The surface area and pore volume of GSBA-15 declined (surface area from 520.8 to 351.9 m2/g and pore volume from 0.707 to 0.564 cm3/g) after ZnO impregnation due to pore blocking. At the same time, increasing pore diameter (from 2.82 nm to 3.19 nm) and crystallite size (from 5.1 nm to 12.6 nm) were observed due to the overlapping of ZnO-Silica particles. The increasing incorporation of ZnO on the silica GSBA-15 framework increases the photodegradation performance from 88.76% to 94.90% due to the high surface area, functional group rich, and dispersion of ZnO active sites. 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). 
Synthesis and Characterization of Mesoporous Carbon Supported Ni-Ga Catalyst for Low-Pressure CO2 Hydrogenation Uwin Sofyani; Yuni Krisyuningsih Krisnandi; Iman Abdullah
Bulletin of Chemical Reaction Engineering & Catalysis 2022: BCREC Volume 17 Issue 2 Year 2022 (June 2022)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.17.2.13377.278-285

Abstract

In this study, the atmospheric-pressure hydrogenation of CO2 was carried over bimetallic Ni-Ga catalyst supported on mesoporous carbon (MC). MC was successfully prepared using the soft-template method as proven by Fourier Transform Infra Red (FTIR), X-ray Diffraction (XRD), Scanning Electron Microscopy - Energy Dispersive X-Ray Spectroscopy (SEM-EDS), Brunauer–Emmett–Teller  Surface Area Analyzer (BET SAA), and Transmission Electron Microscopy (TEM) characterizations. The Ni-Ga/MC catalyst was synthesized using the impregnation method, and based on the XRD characterization, the formation of bimetallic Ni-Ga on the MC support is confirmed. The EDS mapping image shows the uniform distribution of the bimetallic Ni-Ga on the MC surface, especially for the Ni5Ga3/MC and NiGa3/MC catalysts. Moreover, the TEM images show an excellent pore size distribution. The formation of Ni-Ga alloy was identified as an active site in the CO2 hydrogenation. Ni5Ga3/MC catalyst exhibited a 10.80% conversion of CO2 with 588 μmol/g formaldehyde at 1 atm, 200 °C, and H2/CO2 ratio of 3/1. 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). 
Experimental and Kinetic Modeling of Galactose Valorization to Levulinic Acid Retno Ringgani; Muhammad Mufti Azis; Rochmadi Rochmadi; Arief Budiman
Bulletin of Chemical Reaction Engineering & Catalysis 2022: BCREC Volume 17 Issue 2 Year 2022 (June 2022)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.17.2.14032.451-465

Abstract

Levulinic acid, a versatile chemical building block, was derived from C6-sugar galactose using sulfuric acid as the catalyst. Galactose is monosaccharide of polysaccharides constituent that is mostly contained in third generation biomass, macro-microalgae. It currently receives high attention to be a source of renewable feedstock. The effect of temperature, catalyst concentration and initial substrate loadings were studied for 60 min, in the temperature range of 150–190 °C, acid concentration of 0.25–0.75 M and initial substrate loading of 0.05–0.25 M. The highest levulinic acid yield of 40.08 wt% was achieved under the following conditions: 0.05 M galactose, 0.75 M acid concentration, 170 °C temperature, and 40 min reaction time. The kinetic model was developed by first order pseudo-irreversible reaction. The results showed that the proposed model could capture the experimental data well. These results suggested that galactose, derived from macro- and micro-algae, can potentially be converted and applied for platform chemicals. 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). 
Hydrothermal Synthesis and Photocatalytic Activity of NiO Nanoparticles under Visible Light Illumination J. Anita Lett; Suresh Sagadevan; Getu Kassegn Weldegebrieal; Is Fatimah
Bulletin of Chemical Reaction Engineering & Catalysis 2022: BCREC Volume 17 Issue 2 Year 2022 (June 2022)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.17.2.13680.340-349

Abstract

In this present study, Nickel oxide (NiO) nanoparticles (NPs) have been synthesized using the hydrothermal method and characterized using powder X-ray Diffraction (XRD), UV-vis and Fourier Transform Infra Red (FTIR) spectroscopies, Scanning Electron Microscopy (SEM), and Energy-Dispersive X-ray (EDX) methods. The result of the characterization indicates that the synthesized sample has a pure cubic phase of NiO with roughly spherical shape morphologies and respective estimated crystallinity and microstrain values of about 78% and 5.1. Test of the photocatalytic activity of the synthesized sample towards the model contaminant dye methylene blue (MB) shows a degradation efficiency of 46% in a period of 2 h under nature sunlight irradiation at natural pH and that the reaction could satisfactorily describe both pseudo-first-order and pseudo-second-order kinetic models. So, this synthesis method may potentially be used for the effective elimination of toxic organic pollutants from water and wastewater over prolonged exposure under natural sunlight without adding any oxidant or adjusting the pH of the reaction medium. 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). 
Sodium Silicate Catalyst for Synthesis Monoacylglycerol and Diacylglycerol-Rich Structured Lipids: Product Characteristic and Glycerolysis–Interesterification Kinetics Inasanti Pandan Wangi; Supriyanto Supriyanto; Hary Sulistyo; Chusnul Hidayat
Bulletin of Chemical Reaction Engineering & Catalysis 2022: BCREC Volume 17 Issue 2 Year 2022 (June 2022)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.17.2.13306.250-262

Abstract

Sodium silicate as heterogeneous base catalysts is more environmentally friendly and easily separated by filtration. The objective of this research was to evaluate the activated sodium silicate as catalyst for synthesis of monoacylglycerol (MAG) and diacylglycerol (DAG)-rich structured lipids (SLs) from a palm olein-stearin blend. Sodium silicate was activated and functional group was characterized. Reaction was performed using 5% catalyst (w/w) at various reaction temperature (70–120 °C) for 3 h in a batch stirred tank reactor. Physical properties of SLs, such as melting point, slip melting point, and hardness of SLs were determined. Reaction kinetics were also evaluated. The results show that Si−O bending was reduced and shifted to a Si−O−Na and Si−O−Si functional groups after sodium silicate activation. Temperature had a significant effect on SLs composition at higher than 90 °C. An increase in temperature produced more MAG, resulting in better product physical properties. The best reaction condition was at 110 °C. Rate constants and the Arrhenius equation were also obtained for each reaction step. In summary, the activated sodium silicate catalyzed glycerolysis-interesterification reaction, which produced MAG and DAG at temperature higher than 90 °C. Therefore, the physical properties of SLs were improved. 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). 

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