cover
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 16 Documents
Search results for , issue "2022: BCREC Volume 17 Issue 3 Year 2022 (September 2022)" : 16 Documents clear
Insights into the Titania (TiO2) Photocatalysis on the Removal of Phthalic Acid Esters (PAEs) in Water Norfarahim Mohd Tubillah; Sheela Chandren
Bulletin of Chemical Reaction Engineering & Catalysis 2022: BCREC Volume 17 Issue 3 Year 2022 (September 2022)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.17.3.15385.608-626

Abstract

In this era of globalization, plastic is regarded as one of the most versatile innovations, finding its uses ranging from packaging, automotive, agriculture, and construction to the medical and pharmaceutical industries. Unfortunately, the single-use nature of plastics leads to ecological and environmental problems. Among conventional disposal management of plastic waste are landfilling dumping, incineration, and recycling. However, not all plastic waste goes into disposal management and ends up accumulating in lakes, rivers, and seas. In the aquatic environment, the action of photochemical weathering plastics has resulted in the release of chemical additives such as phthalic acid esters (PAEs), an important plasticizer added to plastic products to improve their softness, flexibility, and durability. Nowadays, PAEs have been ubiquitously detected in our environment and numerous organisms are exposed to PAEs to some extent. As PAEs carry endocrine disruptive and carcinogenicity properties, an urgent search for the development of an efficient and effective method to remove PAEs from the environment is needed. As a viable option, titania (TiO2) photocatalysis is a promising tool to combat the PAEs contamination in our environment owing to its high photocatalytic activity, cost-effectiveness, and its ability to totally mineralize PAEs into carbon dioxide and water. Hence, this paper aims to highlight the concerning issue of the contamination of PAEs in our aquatic environments and the summary of the removal of PAEs by TiO2 photocatalysis. This review concerning the significance of knowledge on environmental PAEs would hopefully spark huge interest and future development to tackle this plastic-associated pollutant. 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). 
Reusable Catalyst of KF/Mg-Al Layered Double for Biodiesel Conversion and Optimization using Bohn-Behnken Design Totok Eka Suharto; Fethi Kooli; Sheikh Ahmad Izaddin Sheikh Mohd Ghazali; Is Fatimah
Bulletin of Chemical Reaction Engineering & Catalysis 2022: BCREC Volume 17 Issue 3 Year 2022 (September 2022)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.17.3.14485.497-507

Abstract

This work aimed to synthesize a reusable catalyst of KF/Mg-Al layered double hydroxide (KF/LDH) for a microwave-assisted biodiesel conversion from rice bran oil (RBO). The LDH was synthesized by co-precipitation method of Mg and Al precursors with additional surfactant of cetyl trimethyl ammonium followed by hydrothermal method, for furthermore, an impregnation procedure was applied to combine KF with LDH by using impregnation method. Instrumental analysis of materials was performed by XRD, gas sorption analysis, SEM-EDX, TEM and XPS method. Effect of KF loading onto LDH on the specific surface area and solid basicity was also studied. From the characterization by XRD, it can be concluded that the impregnation increased specific surface area of LDH without any structural destruction, which was also confirmed by the lattice fringe comparison by HRTEM analysis and surface analysis by XPS. The specific surface area enhancement is in line with the increasing solid basicity which directly enhanced the catalytic conversion of RBO into biodiesel. Statistical optimization of the use of KF/LDH was conducted by response surface methodology of Box-Behnken Design for the range of 2–4 g/100 mL of catalyst dose, 3–8 of the methanol to oil ratio, and 10–30 min of reaction time. It was revealed that all factors are significantly affect the yield. The KF/LDH catalyst is also reusable as it does not loss the activity until 5th cycles. 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). 
Catalytic Dye Oxidation over CeO2 Nanoparticles Supported on Regenerated Cellulose Membrane Tran Thi Thuy; Dinh Ngoc Duong; Nguyen Quynh Vi; Nguyen Duc Duong; Tran Duc Thinh; Nguyen Cong Bang; Pham Hung Vuong; Nguyen Ngoc Mai
Bulletin of Chemical Reaction Engineering & Catalysis 2022: BCREC Volume 17 Issue 3 Year 2022 (September 2022)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.17.3.15384.554-564

Abstract

A novel regenerated cellulose (RC) membrane containing cerium oxide (CeO2) nanoparticles is described in detail. In this work, CeO2 nanoparticles with high surface area and mesoporosity were prepared by a modified template-assisted precipitation method. Successful synthesis was achieved using cerium nitrate as a precursor, adjusting the final pH solution to around 11 by ammonium hydroxide and ethylene diamine, and annealing at 550 °C for 3 hours under a protective gas flow. This resulted in a surface area of 55.55 m².g–1 for the nanoparticles. The regenerated cellulose membrane containing CeO2 particles was synthesized by the novel and environmentally friendly method. The catalyst CeO2 and cellulose/CeO2 membrane were characterized by Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), Electron paramagnetic resonance (EPR), and Brunauer-Emmett-Teller (BET) measurements. The g-value of 2.276 has confirmed the presence of the surface superoxide species of CeO2 nanoparticles in EPR. The photocatalytic activity of the catalyst and the membrane containing the catalyst was evaluated through the degradation of methylene blue under visible light irradiation by UV-VIS measurements. The cellulose/CeO2 membrane degraded 80% of the methylene blue solution in 120 minutes, showing a better photocatalytic activity than the CeO2 catalyst, which degraded approximately 62% in the same period. It has been proven that the RC membrane is not only a good transparent supporting material but also a good adsorption for high-performance of CeO2 catalyst. 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 of ZnO-Fe3O4 Magnetic Nanocomposites through Sonochemical Methods for Methylene Blue Degradation Nanda Saridewi; Sri Komala; Agustino Zulys; Siti Nurbayti; Latifah Tulhusna; Adawiah Adawiah
Bulletin of Chemical Reaction Engineering & Catalysis 2022: BCREC Volume 17 Issue 3 Year 2022 (September 2022)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.17.3.15492.650-660

Abstract

Textile industry waste can pollute the aquatic environment because it contains dye contaminants with very stable properties that are difficult to degrade naturally. However, dye contaminants degradation can be carried out by photodegradation using ZnO-Fe3O4 magnetic nanocomposite photocatalysts. This study aims to synthesize ZnO-Fe3O4 magnetic nanocomposite through a sonochemical method. Then measure their photocatalytic activity in methylene blue degradation. The best ZnO-Fe3O4 magnetic nanocomposite is made of ZnO:Fe3O4 mass ratio of 4:1 with a crystal size of 31.058 nm, a hexagonal crystal phase and a particle size of 173.23 nm. The ZnO-Fe3O4 magnetic nanocomposites (4:1) provides optimum degradation capacity of methylene blue under halogen lamp irradiation of 99.56 mg/g at pH 13. Furthermore, the ZnO-Fe3O4 magnetic nanocomposites had good stability in 10 cycles reaction with a degradation capacity of 99.24-99.75 mg/g. The photocatalytic degradation of methylene blue by ZnO-Fe3O4 occurs through the formation of free radical species with hydroxyl radicals as the dominant species that play an important role in the degradation process. 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). 
Thermodynamic Study of One-step Production from Isobutene to Methyl Methacrylate Lik Quan Lau; Sin Yuan Lai; Haiyan Li; Cheng Loong Ngan; Mahashanon Arumugam; Mukhamad Nurhadi
Bulletin of Chemical Reaction Engineering & Catalysis 2022: BCREC Volume 17 Issue 3 Year 2022 (September 2022)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.17.3.15574.590-607

Abstract

Methyl methacrylate (MMA) has emerged as an essential industrial monomer. However, the toxic by-production and shortage supply of MMA in the global market has gained great attention. Herein, a one-step synthesis to produce MMA from isobutene via a direct oxidative esterification process has been demonstrated to curb the aforementioned downsides. Thermodynamic analysis via Gibbs free energy minimization method proved the feasibility of this route via the equilibrium constant. Despite tert-butanol and isobutane showed higher equilibrium constant than isobutene, they should be avoided. Isobutane is highly flammable while the precursor of tert-butanol is exorbitant. Thus, isobutene was selected for the equilibrium compositions screening. Isobutene conversion was 90% and 15% MMA yield at 700 °C and IBN: O2: MeOH ratio with 1:7:1. This route is mainly limited by the generation of side reactions from the reaction of CH3OH and O2. By varying the feedstock ratio at 1:2:1, the MMA yield increased to ~25%. 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). 
Investigating the Interaction between Methanol and the Heulandite-type Zeolite using First Principle Molecular Dynamic Fiska Dewi Wulandhani; Fajar Inggit Pambudi
Bulletin of Chemical Reaction Engineering & Catalysis 2022: BCREC Volume 17 Issue 3 Year 2022 (September 2022)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.17.3.15169.542-553

Abstract

The interaction between methanol and the Heulandite-type zeolite has been unveiled to give an atomic scale detail regarding the catalytic activity of this zeolite for methanol conversion. The study was carried out by first principle molecular dynamics to get an insight into the structure and electronic behaviour of methanol inside the zeolite structure at different temperatures. The behaviour of methanol was studied when the location of the proton of Bronsted acid sites was varied to give both possible direct and less interaction with methanol. The results show that methanol interacts with the proton from zeolite to give a cationic species of [CH3OH2]+ both in 300K and 573K conditions. However, when the proton is located at different location far from possible interaction with methanol, the formation of a cationic species is hindered. This study provides an insight into the design of Heulandite type zeolite to give a catalytic activity toward methanol transformation.
Photooxidation and Virus Inactivation using TiO2(P25)–SiO2 Coated PET Film Chaowat Autthanit; Supachai Jadsadajerm; Oswaldo Núñez; Purim Kusonsakul; Jittima Amie Luckanagul; Visarut Buranasudja; Bunjerd Jongsomjit; Supareak Praserthdam; Piyasan Praserthdam
Bulletin of Chemical Reaction Engineering & Catalysis 2022: BCREC Volume 17 Issue 3 Year 2022 (September 2022)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.17.3.14180.508-519

Abstract

This study chemically modified PET film surface with P25 using silicate as a binder. Different P25–binder ratios were optimized for the catalyst performance. The modified samples were analyzed by scanning electron microscopy-energy-dispersive X-ray spectroscopy and Fourier transform infrared spectroscopy. Diffuse reflectance UV-vis spectra revealed significant reductions in the band gaps of the P25 solid precursor (3.20 eV) and the surface-modified PET–1.0Si–P25 (2.77 eV) with visible light. Accordingly, under visible light conditions, catalyst activity on the film will occur. Additionally, the film’s performance was evaluated using methylene blue (MB) degradation. Pseudo-first-order-rate constants (min−1), conversion percentages, and rates (µg.mL−1.gcat−1.h−1) were determined. The coated films were evaluated for viral Phi–X 174 inactivation and tested with fluorescence and UV-C light illumination, then log (N/N0) versus t plots (N = [virus] in plaque-forming units [PFUs]/mL) were obtained. The presence of nanosilica in PET showed a high adsorption ability in both MB and Phi–X 174, whereas the best performances with fluorescent light were obtained from PET–1.0Si–P25 and PET–P25–1.0Si–SiO2 equally. A 0.2-log virus reduction was obtained after 3 h at a rate of 4×106 PFU.mL−1.gcat−1.min−1. Additionally, the use of this film for preventing transmission by direct contact with surfaces and via indoor air was considered. Using UV light, the PET–1.0Si–P25 and PET–1.0Si–P25–SiO2 samples produced a 2.5-log inactivation after 6.5 min at a rate of 9.6×106 and 8.9×106 PFU.mL−1.gcat−1.min−1, respectively. 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). 
Silicate Scaling Formation: Impact of pH in High-Temperature Reservoir and Its Characterization Study Rozana Azrina Sazali; Kenneth Stuart Sorbie; lorraine Scott Boak; Nurshazwani Shuhada Al Badri; Harumi Veny; Farah Hanim Ab Hamid; Mohd Zaki Zainal Abidin
Bulletin of Chemical Reaction Engineering & Catalysis 2022: BCREC Volume 17 Issue 3 Year 2022 (September 2022)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.17.3.15290.661-682

Abstract

Silicate scaling tends to form and be aggravated during high pH Alkaline Surfactant Polymer (ASP) floods and this silicate scale deposition affects oil production. Hence, it is important to examine the conditions that lead to silicate scale forming. The severity of the silicate scaling reaction, the type and morphology of silica/silicate scale formed in an experimental ASP flood were studied for pH values 5, 8.5, and 11, whilst the temperature was kept constant at 90 ℃. In addition, the impact of calcium ion was studied and spectroscopic analyses were used to identify the extent of scaling reaction, morphology type and the functional group present in the precipitates. This was performed using imagery of the generated precipitates. It was observed that the silica/silicate scale is most severe at the highest pH and Ca:Mg molar ratios examined. Magnesium hydroxide and calcium hydroxide were observed to precipitate along with the silica and Mg-silicate/Ca-silicate scale at pH 11. The presence of calcium ions altered the morphology of the precipitates formed from amorphous to microcrystalline/crystalline. In conclusion, pH affects the type, morphology, and severity of the silica/silicate scale produced in the studied scaling system. The comprehensive and conclusive data showing how pH affects the silicate scaling reaction reported here are vital in providing the foundation to further investigate the management and prevention of this silicate scaling. 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)
Comparative Adsorption Performance of Carbon-containing Hydroxyapatite Derived Tenggiri (Scomberomorini) and Belida (Chitala) Fish Bone for Methylene Blue Sri Lestari; Mukhamad Nurhadi; Ratna Kusuma Wardani; Eko Saputro; Retno Pujisupiati; Nova Sukmawati Muskita; Nezalsa Fortuna; A’an Suri Purwandari; Fahria Aryani; Sin Yuan Lai; Hadi Nur
Bulletin of Chemical Reaction Engineering & Catalysis 2022: BCREC Volume 17 Issue 3 Year 2022 (September 2022)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.17.3.15303.565-576

Abstract

The utilization of fishbone as the carbon source for methylene blue adsorption has been successfully studied. Fishbone was prepared from two kinds of fish such as marine fisheries (ex. Tenggiri) and freshwater fisheries (ex. Belida). The carbons were prepared by carbonation of fishbone powder at  500 °C for 2 h. Physical properties of carbons were characterized using Fourier transform infrared (FTIR) spectroscopy, X-ray diffraction (XRD), wavelength dispersive X-ray fluorescence (WDXRF), Scanning Electron Microscope (SEM), and hydrophobicity. The carbons were utilized as the adsorbent for removing methylene blue by varying the contact time, initial dye concentration, and temperature. It is concluded that both carbons can very good adsorb the methylene blue. The adsorption performance of carbon (TFC) from Tenggiri fish is better than carbon (BFC) from Belida fish. The adsorption was well fitted with the Langmuir adsorption model (R2 ~ 0.998) and the pseudo-second-order model. This indicated that the dye molecules were adsorbed on the surface-active site of carbon via chemical binding, forming an adsorbate monolayer. Thermodynamic parameters, including the Gibbs free energy (ΔG), enthalpy (ΔH), and entropy (ΔS), indicated that the adsorption of methylene blue onto the carbon from fishbone was spontaneous. Thus, carbon from fishbone can be applied as a low-cost adsorbent to treat industrial effluents contaminated with methylene blue. 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). 
Enhancement in Photocatalytic Efficiency of Commercial TiO2 Nanoparticles by Calcination: A Case of Doxycycline Removal Nguyen Thi Cam Tien; Chau Hong Nhut; Vo Thi Thanh Thuy; Trinh Thi Bich Huyen; Lam Pham Thanh Hien; Nguyen Nhat Huy
Bulletin of Chemical Reaction Engineering & Catalysis 2022: BCREC Volume 17 Issue 3 Year 2022 (September 2022)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.17.3.13970.486-496

Abstract

In this study, the pure and calcined forms of Degussa TiO2 were applied for photocatalytic removal of doxycycline - a broad-spectrum tetracycline antibiotic. The calcination of TiO2 at 500 °C enhanced the photocatalytic efficiency of the TiO2 under optimal operational conditions of 5 ppm of doxycycline, 0.25 g/L of TiO2, pH 6.5, 120 min, and room temperature. In addition, the changes in morphology, crystal structure, and optical properties of the materials before and after calcination were observed by scanning electron microscopy, X-ray diffraction, and UV-Visible spectroscopy. The reaction kinetics of the doxycycline removal was also investigated based on the Langmuir-Hinshelwood model with a correlation coefficient R2 of >80%. Results showed that the photocatalytic ability of TiO2 is stable and enhanced after being calcined at a suitable temperature of 500 °C. This opens up the potential application of TiO2 in the treatment of emerging organic pollutants in water. 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). 

Page 1 of 2 | Total Record : 16


Filter by Year

2022 2022


Filter By Issues
All Issue 2024: BCREC Volume 19 Issue 1 Year 2024 (April 2024) 2024: Just Accepted Manuscript and Article In Press 2024 2023: BCREC Volume 18 Issue 4 Year 2023 (December 2023) 2023: BCREC Volume 18 Issue 3 Year 2023 (October 2023) 2023: BCREC Volume 18 Issue 2 Year 2023 (August 2023) 2023: BCREC Volume 18 Issue 1 Year 2023 (April 2023) 2022: BCREC Volume 17 Issue 4 Year 2022 (December 2022) 2022: BCREC Volume 17 Issue 3 Year 2022 (September 2022) 2022: BCREC Volume 17 Issue 2 Year 2022 (June 2022) 2022: BCREC Volume 17 Issue 1 Year 2022 (March 2022) 2021: BCREC Volume 16 Issue 4 Year 2021 (December 2021) 2021: BCREC Volume 16 Issue 3 Year 2021 (September 2021) 2021: BCREC Volume 16 Issue 2 Year 2021 (June 2021) 2021: BCREC Volume 16 Issue 1 Year 2021 (March 2021) 2020: BCREC Volume 15 Issue 3 Year 2020 (December 2020) 2020: BCREC Volume 15 Issue 2 Year 2020 (August 2020) 2020: BCREC Volume 15 Issue 1 Year 2020 (April 2020) 2019: BCREC Volume 14 Issue 3 Year 2019 (December 2019) 2019: BCREC Volume 14 Issue 2 Year 2019 (August 2019) 2019: BCREC Volume 14 Issue 1 Year 2019 (April 2019) 2018: BCREC Volume 13 Issue 3 Year 2018 (December 2018) 2018: BCREC Volume 13 Issue 2 Year 2018 (August 2018) 2018: BCREC Volume 13 Issue 1 Year 2018 (April 2018) 2017: BCREC Volume 12 Issue 3 Year 2017 (December 2017) 2017: BCREC Volume 12 Issue 2 Year 2017 (August 2017) 2017: BCREC Volume 12 Issue 1 Year 2017 (April 2017) 2016: BCREC Volume 11 Issue 3 Year 2016 (December 2016) 2016: BCREC Volume 11 Issue 2 Year 2016 (August 2016) 2016: BCREC Volume 11 Issue 1 Year 2016 (April 2016) 2015: BCREC Volume 10 Issue 3 Year 2015 (December 2015) 2015: BCREC Volume 10 Issue 2 Year 2015 (August 2015) 2015: BCREC Volume 10 Issue 1 Year 2015 (April 2015) 2014: BCREC Volume 9 Issue 3 Year 2014 (December 2014) 2014: BCREC Volume 9 Issue 2 Year 2014 (August 2014) 2014: BCREC Volume 9 Issue 1 Year 2014 (April 2014) 2013: BCREC Volume 8 Issue 2 Year 2013 (December 2013) 2013: BCREC Volume 8 Issue 1 Year 2013 (June 2013) 2013: BCREC Volume 7 Issue 3 Year 2013 (March 2013) 2012: BCREC Volume 7 Issue 2 Year 2012 (December 2012) 2012: BCREC Volume 7 Issue 1 Year 2012 (June 2012) 2011: BCREC Volume 6 Issue 2 Year 2011 (December 2011) 2011: BCREC Volume 6 Issue 1 Year 2011 (June 2011) 2010: BCREC Volume 5 Issue 2 Year 2010 (December 2010) 2010: BCREC Volume 5 Issue 1 Year 2010 (June 2010) 2009: BCREC Volume 4 Issue 2 Year 2009 (December 2009) 2009: BCREC Volume 4 Issue 1 Year 2009 (June 2009) 2008: BCREC Volume 3 Issue 1-3 Year 2008 (December 2008) 2007: BCREC: Volume 2 Issues 2-3 Year 2007 (October 2007) 2007: BCREC: Volume 2 Issue 1 Year 2007 (June 2007) More Issue