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Bulletin of Chemical Reaction Engineering & Catalysis
Published by Masyarakat Katalis Indonesia - Indonesian Catalyst Society
ISSN : -     EISSN : 19782993     DOI : https://doi.org/10.9767/bcrec
Core Subject : Science, Engineering,
Chemical Engineering, Chemistry & Bioengineering Chemistry
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.
Arjuna Subject : Teknik Kimia (semua kategori) - Katalisis
Articles 838 Documents
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Corrigendum to: Characterization of Industrial Pt-Sn/Al2O3 Catalyst and Transient Product Formations during Propane Dehydrogenation [8(1), (2013), 77-82]
Bulletin of Chemical Reaction Engineering & Catalysis 2014: BCREC Volume 9 Issue 2 Year 2014 (August 2014)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.9.2.7136.155

Abstract

Corrigendum to: Kah, S.H., Joanna Jo, E.C., Sim, Y.C., Chin, K.C. (2013). Bulletin of Chemical Reaction Engineering & Catalysis, 8(1): 77-82. (doi:10.9767/bcrec.8.1.4569.77-82). In Abstract, typed as: “….. Due to information paucity, the physicochemical characteristics of the commercially obtained regener-ated Pt-Sn/Al2O3 catalyst (operated in moving bed reactor) and coke formation at different tempera-tures of reaction were discussed…..”In the Abstract, the phrase of “(operated in moving bed reactor)” should be deleted.Erratum: Kah, S.H., Joanna Jo, E.C., Sim, Y.C., Chin, K.C. (2013). Bulletin of Chemical Reaction Engineering & Catalysis, 8(1): 77-82. (doi:10.9767/bcrec.8.1.4569.77-82).In Abstract section, the phrase of “(operated in moving bed reactor)” was deleted.Therefore, the sentence in the Abstract was corrected to: “….. Due to information paucity, the physico-chemical characteristics of the commercially obtained regenerated Pt-Sn/Al2O3 catalyst and coke for-mation at different temperatures of reaction were discussed…..”.© 2014 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 Hydrogenation of Levulinic Acid in Water into g-Valerolactone over Bulk Structure of Inexpensive Intermetallic Ni-Sn Alloy Catalysts Rodiansono Rodiansono; Maria Dewi Astuti; Abdul Ghofur; Kiky C. Sembiring
Bulletin of Chemical Reaction Engineering & Catalysis 2015: BCREC Volume 10 Issue 2 Year 2015 (August 2015)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.10.2.8284.192-200

Abstract

A bulk structure of inexpensive intermetallic nickel-tin (Ni-Sn) alloys catalysts demonstrated highly selective in the hydrogenation of levulinic acid in water into g-valerolactone. The intermetallic Ni-Sn catalysts were synthesized via a very simple thermochemical method from non-organometallic precursor at low temperature followed by hydrogen treatment at 673 K for 90 min. The molar ratio of nickel salt and tin salt was varied to obtain the corresponding Ni/Sn ratio of 4.0, 3.0, 2.0, 1.5, and 0.75. The formation of Ni-Sn alloy species was mainly depended on the composition and temperature of H2 treatment. Intermetallics Ni-Sn that contain Ni3Sn, Ni3Sn2, and Ni3Sn4 alloy phases are known to be effective heterogeneous catalysts for levulinic acid hydrogenation giving very excellence g-valerolactone yield of >99% at 433 K, initial H2 pressure of 4.0 MPa within 6 h. The effective hydrogenation was obtained in H2O without the formation of by-product. Intermetallic Ni-Sn(1.5) that contains Ni3Sn2 alloy species demonstrated very stable and reusable catalyst without any significant loss of its selectivity. © 2015 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/NiO/g-C3N4 Nanocomposite Materials for Photocatalytic Degradation of Tetracycline Antibiotic Nong, Linh X.; Nguyen, Oanh Thi Kim
Bulletin of Chemical Reaction Engineering & Catalysis 2023: BCREC Volume 18 Issue 4 Year 2023 (December 2023)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.20039

Abstract

In this study, an approach was utilized to improve the photocatalytic efficacy of g-C3N4 by creating a composite photocatalyst through co-precipitation. This process involved incorporating NiO and ZnO into the structure, resulting in enhanced photocatalytic activity. The Scanning Electron Microscopy (SEM) showcases interesting aggregation behavior, revealing extensive arrays of ZnO/NiO/g-C3N4 particles. Ultraviolet–Visible Diffuse Reflectance Spectroscopy (UV-Vis DRS) confirms the composite's strong light absorption, especially in the visible spectrum. X-ray diffraction (XRD) analysis provides conclusive evidence of successful material synthesis. The degradation of tetracycline antibiotics under visible light exposure demonstrates an impressive photochemical degradation efficiency of 78.43%. Additionally, the composite exhibits impressive cycles of reuse, retaining its high photocatalytic activity even after four reaction cycles. This performance surpasses that of comparison samples. The synergistic integration of NiO and g-C3N4 within ZnO proves to be crucial in enhancing photocatalytic activity by enhancing electron-hole separation and mitigating recombination processes. This composite photocatalyst shows a wide potential for efficiently eliminating tetracycline antibiotics from water systems. Copyright © 2023 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). 
Environmental Footprint Assessment of Methylene Blue Photodegradation using Graphene-based Titanium Dioxide Kelvert Kong; Ying Weng; Weng Hoong Lam; Sin Yuan Lai
Bulletin of Chemical Reaction Engineering & Catalysis 2023: BCREC Volume 18 Issue 1 Year 2023 (April 2023)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.17450

Abstract

To date, photocatalysis has received much attention in terms of the degradation of organic pollutants in wastewater. Various studies have shown that graphene-based photocatalysts are one of the impressive options owing to their intriguing features, including high surface area, good conductivity, low recombination rate of electron-hole pair, and fast charge separation and transfer. However, the environmental impacts of the photocatalysts synthesis and their photodegradation activity remain unclear. Thus, this report aims to identify the environmental impacts associated with the photodegradation of methylene blue (MB) over reduced graphene oxide/titanium oxide photocatalyst (TiO2/rGO) using Life Cycle Assessment (LCA). The life cycle impacts were assessed using ReCiPe 2016 v1.1 midpoint method, Hierachist version in Gabi software. A cradle-to-gate approach and a functional unit of 1 kg TiO2/rGOwere adopted in the study. Several important parameters, such as the solvent type (ultrapure water, ethanol, and isopropanol), with/without silver ion doping, and visible light power consumption (150, 300, and 500 W) were evaluated in this study. In terms of the selection of solvent, ultrapure water is certainly a better choice since it contributed the least negative impact on the environment. Furthermore, it is not advisable to dope the photocatalyst with silver ions since the increment in performance is insufficient to offset the environmental impact that it caused. The results of different power of visible light for MB degradation showed that the minimum power level, 150 W, could give a comparable photodegradation efficiency and better environmental impacts compared to higher power light sources. Copyright © 2023 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). 
Biochar-Modified Layered Double Hydroxide for Highly Efficient on Phenol Adsorption Amri Amri; Rezonsi Rezonsi; Nur Ahmad; Tarmizi Taher; Neza Rahayu Palapa; Risfidian Mohadi; Aldes Lesbani
Bulletin of Chemical Reaction Engineering & Catalysis 2023: BCREC Volume 18 Issue 3 Year 2023 (October 2023)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.19898

Abstract

All activities require drinking water. The existence of waste makes water unfit for consumption. Phenol waste is one example of waste that is often found. The toxic and corrosive nature of phenol is very dangerous for life, so its presence must be considered. The adsorption process was carried out using NiAl and ZnAl layered double hydroxides composites with biochar to eliminate the presence of phenol waste The adsorption process was carried out using NiAl and ZnAl layered double hydroxydes materials which were composited with biochar to eliminate the presence of phenol waste. NiAl-Biochar and ZnAl-Biochar composites were successfully prepared, as determined by XRD, FTIR, SEM, and BET analyses. NiAl layered double hydroxide surface area grew from 92.683 to 438.942 m2/g while ZnAl layered double hydroxide surface area increased from 9.621 to 58.461 m2/g. pHpzc of material is between 5.1 and 9.4. Optimal pH of NiAl and ZnAl layered double hydroxide is 3, optimum pH of NiAl-Biochar and ZnAl-Biochar is 5, and optimum pH of Biochar is 7. All kinetic and isotherm models for all materials were pseudo-second-order and Freundlich, respectively. NiAl-Biochar and ZnAl-Biochar have maximal adsorption capacities of 74.62 mg/g and 52.91 mg/g, respectively. The material's reusability indicates that NiAl-Biochar has superior qualities and may be reused for up to five cycles, followed by ZnAl-Biochar, NiAl layered double hydroxide, ZnAl layered double hydroxide, and Biochar. Copyright © 2023 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). 
Vulcanization Kinetics and Mechanical Properties of Ethylene Propylene Diene Monomer Thermal Insulation Mohamad Irfan Fathurrohman; Dadi Rusadi Maspanger; Sutrisno Sutrisno
Bulletin of Chemical Reaction Engineering & Catalysis 2015: BCREC Volume 10 Issue 2 Year 2015 (August 2015)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.10.2.6682.104-110

Abstract

The vulcanization kinetics of Ethylene-propylene diene monomer (EPDM) rubber thermal insulation was studied by using rheometer under isothermal condition at different temperatures. The rheometry analysis was used to determining the cure kinetic parameters and predicting the cure time of EPDM thermal insulation. The experimental results revealed that the curing curves of EPDM thermal insulation were marching and the optimum curing time decreased with increasing the temperature. The kinetic parameters were determined from the autocatalytic model showed close fitting with the experimental results, indicating suitability of autocatalytic model in characterizing the cure kinetics. The activation energy was determined from the autocatalytic model is 46.3661 kJ mol-1. The cure time were predicted from autocatalytic model and the obtained kinetic parameter by using the relationship among degree of conversion, cure temperature, and cure time. The predictions of cure time provide information for the actual curing characteristic of EPDM thermal insulation. The mechanical properties of EPDM thermal insulation with different vulcanization temperatures showed the same hardness, tensile strength and modulus at 300%, except at temperature 70 °C, while the elongation at breaking point decreased with increasing temperature of vulcanization. © 2015 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)
One-Pot Access to Diverse Functionalized Pyran Annulated Heterocyclic Systems Using SCMNPs@BPy-SO3H as a Novel Magnetic Nanocatalyst Ke Chen; Guangzu He; Qiong Tang; Qahtan A. Yousif
Bulletin of Chemical Reaction Engineering & Catalysis 2020: BCREC Volume 15 Issue 2 Year 2020 (August 2020)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.15.2.6693.348-366

Abstract

The SCMNPs@BPy-SO3H catalyst was prepared and characterized using Fourier Transform Infrared Spectroscopy (FTIR), Thermogravimetric Analysis (TGA), Vibrating Sample Magnetometry (VSM), Energy Dispersive X-ray Spectroscopy (EDX), X-ray Diffraction (XRD), and Scanning Electron Microscopy (SEM). Afterwards, its capability was efficiently used to promote the one-pot, three-component synthesis of pyrano[2,3-c]pyrazole and 2-amino-3-cyano-pyrano[3,2-c]chromen-5(4H)-one derivatives. The strategy resulted in the desired products with excellent yields and short reaction times. The SCMNPs@BPy-SO3H catalyst was readily recovered using a permanent magnetic field and it was reused in six runs with a slight decrease in catalytic activity. Copyright © 2020 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).
Application of Ionic Liquid [DMIM]DMP Pretreatment in the Hydrolysis of Sugarcane Bagasse for Biofuel Production Arief Widjaja; Silvya Yusnica Agnesty; Hanny F. Sangian; Setiyo Gunawan
Bulletin of Chemical Reaction Engineering & Catalysis 2015: BCREC Volume 10 Issue 1 Year 2015 (April 2015)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.10.1.7143.70-77

Abstract

Sugarcane bagasse is one of lignocellulose materials that can be converted to biofuel. This work was aimed to develop new pretreatment combination methods to process sugarcane bagasse lignocellulose into biofuel (bio-hydrogen). Pretreatment of sugarcane bagasse using NaOH solution in combination with ionic liquid [DMIM]DMP enhanced the enzymatic hydrolysis significantly. After the pretreat-ment, the content of cellulose and hemicellulose increased by 29.31% compared to the untreated one. Cellulose and hemicelluloses were used as raw materials to produce reducing sugars, that can be con-verted to bio-hydrogen via fermentation. After being subjected to combined pretreatment processes, the crystalline index of sugarcane bagasse decreased significantly compared to solely NaOH pretratment. This indicates a more amorphous structure of the sugarcane bagasse, which makes it is easier to be hy-drolyzed into reducing sugars. The recovery of cellulose + hemicellulose after pretreatment for 20 min and 120 °C was 92%, and the yield obtained was 0.556 g sugars/g (cellulose + hemicellulose) after 12 h and the bio-hydrogen yield was 0.46 mol H2/mol sugars consumed after 48 h fermentation. The use of recycled of ionic liquid showed similar performance compared to the use of fresh ionic liquid. © 2015 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)
Backmatter (Publication Ethics, Copyright Transfer Agreement for Publishing Form)
Bulletin of Chemical Reaction Engineering & Catalysis 2022: BCREC Volume 17 Issue 4 Year 2022 (December 2022)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.17.4.16958.App.1-App.5

Abstract

Synthesis, Crystal Structure, and Catalytic Activity of a Calcium(II) Complex with 4-Formylbenzene-1,3-disulfonate-isonicotinic Acid Hydrazone Xi-Shi Tai; Peng-Fei Li; Li-Li Liu
Bulletin of Chemical Reaction Engineering & Catalysis 2018: BCREC Volume 13 Issue 3 Year 2018 (December 2018)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.13.3.1961.429-435

Abstract

A new calcium(II) complex was synthesized by one-pot synthesis method from disodium 4-formylbenzene-1,3-disulfonate, isonicotinic acid hydrazide and Ca(ClO4)2•2H2O. The structure of calcium(II) complex was determined by elemental analysis, IR and single crystal X-ray diffraction. The results show that the Ca(II) complex molecules form 3D network structure by the interactions of π-π stacking and hydrogen bonds. The Ca(II) complex catalyst could efficiently catalyse oxidation of benzylic alcohol with good conversion of benzyl alcohol (78 %) and excellent selectivity of benzaldehyde (98 %).

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