scholarly journals PENGEMBANGAN PROSES UPGRADING MINYAK BATUBARA: Pengaruh Temperatur, Tekanan dan Space Velocity

2011 ◽  
Vol 7 (1) ◽  
pp. 26
Author(s):  
Yusnitati Yusnitati ◽  
Muhammad Hanif ◽  
M Faizal
Keyword(s):  
Fixed Bed ◽  
Space Velocity ◽  
Liquid Hourly Space Velocity

Minyak batubara cair dengan titik didih 70-360oC, diperoleh dari proses pencairan batubara Tanito Harum menggunakan NEDOL Process skala pilot berkapasitas 150 ton/hari. Minyak batubara cair tersebut diupgrade untuk mengklarifikasi pengaruh temperatur reaksi, tekanan hidrogen, dan liquid hourly space velocity (LHSV) terhadap aktifitas hidrodenitrogenasi. Pengujian dilakukan dalam reactor fixed bed kontinyu berdiameter 8.5 mm menggunakan katalis Ni- W/Alumina pada temperatur 300-375oC, tekanan hidrogen 8-12 MPa, LHSV 0.75-3.0 hr-1 dan rasio hydrogen/oil 1000 NL/L. Hasil pengujian menunjukkan bahwa aktifitas hidrodenitrogenasi meningkat dengan peningkatan temperature reaksi dan tekanan hidrogen. Pada tekanan hidrogen 8 MPa, deaktifasi katalis terjadi lebih cepat dibandingkan dengan tekanan hydrogen 12 MPa selama 15 hari waktu operasi. Selain itu, ditunjukkan pula bahwa pada operasi dengan LHSV yang lebih rendah dan tekanan hidrogen yang lebih tinggi akan lebih efektif untuk menurunkan atau menghilangkan senyawa nitrogen dalam proses upgrading minyak batubara cair. Sehingga, operasi pada tekanan hidrogen 12 MPa diharapkan dapat menghasilkan produk minyak batubara cair dengan kandungan nitrogen yang rendah untuk waktu operasi lebih dari satu tahun pada skala komersial. Kata Kunci: hidrodenitrogenasi, katalis Ni-W/Alumina, minyak batubara cair, upgrading

Dimethyldisulphide Hydrodesulphurization on NiCoMo / Al2O3 Catalyst

2017 ◽  
Vol 68 (7) ◽  
pp. 1496-1500
Author(s):  
Rami Doukeh ◽  
Mihaela Bombos ◽  
Ancuta Trifoi ◽  
Minodora Pasare ◽  
Ionut Banu ◽  
...  
Keyword(s):  
Good Accuracy ◽  
Fixed Bed ◽  
Continuous System ◽  
Space Velocity ◽  
Molar Ratio ◽  
Catalytic Reactor ◽  
Liquid Hourly Space Velocity ◽  
Hydrodesulfurization Process ◽  
Al2o3 Catalyst ◽  
Simplified Kinetic Model

Hydrodesulphurization of dimethyldisulphide was performed on Ni-Co-Mo /�-Al2O3 catalyst. The catalyst was characterized by determining the adsorption isotherms, the pore size distribution and the acid strength. Experiments were carried out on a laboratory echipament in continuous system using a fixed bed catalytic reactor at 50-100�C, pressure from 10 barr to 50 barr, the liquid hourly space velocity from 1h-1 to 4h-1 and the molar ratio H2 / dimethyldisulphide 60/1. A simplified kinetic model based on the Langmuir�Hinshelwood theory, for the dimethyldisulphide hydrodesulfurization process of dimethyldisulphide has been proposed. The results show the good accuracy of the model.

Preparation and Property of Y-Mg-Al-Layered Double Oxides

2011 ◽  
Vol 396-398 ◽  
pp. 764-767
Author(s):  
Tai Xuan Jia ◽  
Ji Chang Zhang ◽  
Zi Li Liu
Keyword(s):  
Condensation Reaction ◽  
Fixed Bed ◽  
Space Velocity ◽  
Precipitation Method ◽  
High Catalytic Activity ◽  
Liquid Hourly Space Velocity ◽  
Maximum Value ◽  
Co Precipitation ◽  
Micro Reactor ◽  
Acetone Condensation

Y-Mg-Al-layered double Oxides (Y-Mg-Al-LDO) were prepared by calcining Y3+-doped Mg-Al-layered hydrotalcites at 823 K for 8 h from co-precipitation method. The samples were detected by XRD and CO2-TPD. Micro-structure and essential regularity were disclosed. The acetone condensation reaction as a probe reaction was carried on fixed-bed micro-reactor at reactive temperature 673 K, reactive time 3 h and liquid hourly space velocity (LHSV) 6 h-1 over Y-Mg-Al-LDO. The catalyst evaluation results show that Y-Mg-Al-LDO possess high catalytic activity. The maximum value of acetone conversion reached 37.53%. The selectivity and single-pass-yield of isophorone were 55.66% and 20.89%, respectively.

Effects of Cu and K Promoters on the Catalytic Performance of Iron-Based Nanocatalyst for Fischer-Tropsch Synthesis

2013 ◽  
Vol 832 ◽  
pp. 15-20 ◽  
Author(s):  
Sara Faiz Hanna Tasfy ◽  
Noor Asmawati Mohd Zabidi ◽  
Duvvuri Subbarao
Keyword(s):  
Atmospheric Pressure ◽  
Fixed Bed ◽  
Space Velocity ◽  
Catalytic Performance ◽  
Reactant Ratio ◽  
Impregnation Method ◽  
Fischer Tropsch ◽  
Heavy Hydrocarbons ◽  
Co Conversion ◽  
Iron Based

Iron-based nanocatalyst was prepared via impregnation method on SiO2 support. The effects of promoters, namely, K and Cu, on the physical properties and catalytic performance in FTS have been investigated. The FTS performance of the synthesized nanocatalysts was examined in a fixed-bed microreactor at temperature of 523K, atmospheric pressure, 1.5 reactant ratio (H2/CO) and space velocity of 3L/g-cat.h. In FTS reaction, Cu promoter resulted in a lower CO conversion and C5+ hydrocarbons selectivity but higher selectivity to the lighter hydrocarbons (C1-C4) comparedto those obtained using the K promoter. Higher CO conversion (28.9%) and C5+ hydrocarbons selectivity (54.4%) were obtained using K as a promoter compared to that of Cu promoter. However, the K-promoted nanocatalyst resulted in a lower CO conversion but higher selectivity of the heavy hydrocarbons (C5+) compared to those obtained using the un-promoted nanocatalyst.

Comparative Study on the Kinetic Modeling of the Oxidative Coupling of Methane in Laboratory and Bench Scales

2008 ◽  
Vol 3 (1) ◽  
Author(s):  
Nakisa Yaghobi ◽  
Mir Hamid Reza Ghoreishy
Keyword(s):  
Kinetic Models ◽  
Oxidative Coupling ◽  
Consumption Rate ◽  
Linear Regression Analysis ◽  
Fixed Bed ◽  
Space Velocity ◽  
Oxidative Coupling Of Methane ◽  
Power Law Model ◽  
Fixed Bed Reactors ◽  
Rate Of Reaction

The aim of this work is to develop and compare kinetic models for the oxidative coupling of methane (OCM) based on the gas hourly space velocity (GHSV) value and CH4/O2 ratio in two scales: laboratory and bench. The experiments were carried out in tubular fixed bed reactors at 1023 K, using 0.7-1.5 g and 30 g of perovskite titanate as the reaction catalyst for laboratory and bench scales, respectively. The various GHSVs (8000, 12000, 17000 h-1) and (3400, 4300, 5200 h-1) and methane to oxygen ratios (1, 2, 3, 4, 7.5) and (2, 2.5, 3) were selected for laboratory and bench scales, respectively. We have proposed a mechanism in which the consumption rate of methane is always twice of production rate of C2. A power law model was assumed for rate of reaction in terms of partial pressure of oxygen and methane. Using a linear regression analysis, the kinetic models were determined. Comparison of the calculated rate of reaction with the experimentally measured data confirmed the accuracy and applicability of the developed model for both scales.

Influence Factors of Denitration Study on Catalyst Mn-Ce/TiO2

2013 ◽  
Vol 634-638 ◽  
pp. 526-530
Author(s):  
Chun Xiang Geng ◽  
Qian Qian Chai ◽  
Wei Yao ◽  
Chen Long Wang
Keyword(s):  
Reaction Temperature ◽  
Catalytic Reduction ◽  
Removal Rate ◽  
Load Capacity ◽  
Fixed Bed ◽  
Influence Factors ◽  
Space Velocity ◽  
Molar Ratio ◽  
Impregnation Method ◽  
Ammonia Gas

Selective Catalytic Reduction (SCR) processes have been one of the most widely used denitration methods at present and the property of low tempreture catalyst becomes a hot research. The Mn-Ce/TiO2 catalyst was prepared by incipient impregnation method. The influence of load capacity, reaction temperature, O2 content, etc. on denitration were studied by a fixed bed catalyst reactor with ammonia gas. Results showed that catalyst with load capacity 18% performed high NO removal rate of 90% at conditions of reaction temperature 160°C, low space velocity, NH3/NO molar ratio 1: 1, O2 concentration 6%.

Production of Hydrogen-Rich Gas Through Pyrolysis of Biomass in a Two-Stage Reactor

2004 ◽  
Author(s):  
Guanyi Chen ◽  
Qiang Li ◽  
Xiaoyang Lv ◽  
Na Deng ◽  
Lifei Jiao
Keyword(s):  
Rice Straw ◽  
Fixed Bed ◽  
Space Velocity ◽  
Corn Stalk ◽  
Two Stage ◽  
Gaseous Products ◽  
Production Of Hydrogen ◽  
Gas Space ◽  
Energy Products ◽  
Pyrolysis Of Biomass

Biomass is quite abundant in the world, particularly in some countries like China. China has large quantities of straw and/or stalk-origin biomass resources and the attention is currently being paid to the exploitation of these resources to produce energy products via different technical solutions, among of which pyrolysis of biomass to produce hydrogen-rich gas is very promising as hydrogen is a very clear energy carrier. In this work, pyrolysis of rice straw, corn stalk and sawdust was carried out in a two-stage reactor (the first-stage reactor is a conventional fixed-bed pyrolyser, and the second-stage reactor is a catalytic fixed bed) to produce hydrogen-rich gas. The effect of catalytic bed on the pyrolysis behaviour have been investigated, with the emphasis on final product particularly hydrogen. The operation of the catalytic reactor appears significant in promoting biomass pyrolysis towards the production of gaseous products, especially hydrogen. At 750°C of the pyrolyser with rice straw as fuel, the use of the catalytic bed leads to the increases of gas yield from 0.41 Nm3/kg to 0.50 Nm3/kg, approximately 22% increase, and of H2 concentration from 33.79% to 50.80% in volume, approximately 50.3% increase, respectively. Compared with calcined dolomite, fresh nickel-based catalyst shows stronger catalytic effect on the pyrolysis of rice straw as its use in the catalytic bed results in the increase of gas yield from 0.41 Nm3/kg to 0.56 Nm3/kg, approximately 36.6% increase, and the increase of H2 concentration from 33.79% to 59.55% in volume, approximately 76.2% increase. Furthermore, two catalysts follow the same trend for the pyrolysis of corn stalk and sawdust. At temperature of 815°C, catalysts also follow the same trend. Catalytic bed can significantly reduce the level of tar which is carried out with the producer gas, to less than 1% of original level. Catalyst load or gas space velocity (hourly) has the influence on the gas yield and H2 concentration. 30% of load, i.e. gas space velocity (hourly) 0.9 × 104 h−1, appears reasonable. Beyond that, gas yield and H2 concentration remain almost unchanged.

Research on the Catalytic Activity of MnyCezOx/TiO2 for Ethyl Acetate Oxidation

2013 ◽  
Vol 781-784 ◽  
pp. 308-311 ◽  
Author(s):  
Xin Li ◽  
Wei Su ◽  
Qi Bin Xia ◽  
Zhi Meng Liu
Keyword(s):  
Catalytic Activity ◽  
Ethyl Acetate ◽  
High Activity ◽  
Fixed Bed ◽  
Space Velocity ◽  
Fixed Bed Reactor ◽  
Impregnation Method ◽  
Acetate Oxidation ◽  
Acetate Concentration ◽  
Molar Ratios

Manganese and cerium based catalysts with different Mn/Ce molar ratios prepared by impregnation method for ethyl acetate oxidation. The activity tests of the samples were performed in a fixed-bed reactor. The effect of gas hourly space velocity (GHSV) and ethyl acetate concentration on the catalytic activity of the catalyst were also investigated. The results showed that these catalysts had high activity for the catalytic oxidation of ethyl acetate, of which the catalyst Mn0.9Ce0.1Ox/TiO2exhibitedthe bestactivity, and the temperature required for 90% conversion of ethyl acetate was at 216 °C. The catalyst Mn0.9Ce0.1Ox/TiO2still maintained high activity in the range of GHSV (16,500 to 48,500 h-1) and ethyl acetate concentration (4526 to 7092 mg/m3). In additional, experiments for measuring stability of Mn0.9Ce0.1Ox/TiO2were carried out, and experimental results showed that the good stability of Mn0.9Ce0.1Ox/TiO2was kept after it has run for 25 hours.

COx Free Hydrogen Production From Ammonia Decomposition Over Platinum Based Siliceous Materials

2012 ◽  
Vol 10 (1) ◽  
Author(s):  
Dilek Varisli ◽  
Tugba Rona
Keyword(s):  
Flow Reactor ◽  
High Surface ◽  
High Surface Area ◽  
Fixed Bed ◽  
Space Velocity ◽  
Decomposition Reaction ◽  
Ammonia Decomposition ◽  
One Pot ◽  
Free Hydrogen ◽  
Synthesis Procedure

Abstract Ammonia has become an important source for hydrogen especially for fuel cell applications that require COx free hydrogen. In this study, high surface area Pt incorporated mesoporous siliceous materials were prepared for ammonia decomposition reaction to produce clean hydrogen. The results of a fixed bed flow reactor tests, conducted using pure ammonia showed that Pt-SiO2 type catalysts which were prepared by a one-pot hydrothermal synthesis procedure were very active in ammonia decomposition, such as 72% conversion was reached at 500°C at a gas hourly space velocity of 5,100 ml/h.gcat over the catalyst prepared at Pt/Si mol ratio of 0.03. Activity of the synthesized catalysts increased with an increase in Pt loading. Platinum incorporated siliceous materials prepared by impregnation procedures were also tested in ammonia decomposition and highly promising results were obtained.

scholarly journals Perfomance of Chromium-Exchanged Zeolite Catalysts in the Combustion of Volatile Organic Compound Pollutants

2004 ◽  
Vol 4 (2) ◽  
pp. 66
Author(s):  
Ahmad Zuhairi Abdullah ◽  
Mohamad Zallani Abu Bakar ◽  
Subhash Bhatia
Keyword(s):  
Resonance Effect ◽  
Coke Formation ◽  
Fixed Bed ◽  
Space Velocity ◽  
Zeolite Catalysts ◽  
Long Run ◽  
Acetate Methyl ◽  
Beta Zeolites ◽  
Volatile Organic ◽  
High Metal

The activity and stability of chromium-exchanged beta (Cr-BEA),mordenite (Cr-MOR), and ZSM-5 (Cr-ZSM-5) zeolites of different Si/Alratios for volatile organic compounds (VOCS) combustion were reported. A fixed-bed catalytic reactor operated between 100 and 500°C and at a gas hourly space velocity (GHSV) of 32,000 h'! was used for the study. Methanol, ethyl acetate, methyl ethyl ketone, benzene, hexane, toluene, and xylene, all at 2,000 ppm, were selected as the VOC model compounds. Oxygenated VOCs were more reactive while showing good carton dioxide yield. Aromatics were more stable due to their resonance effect but the reactivity increased with the attachment of an electron donor group such as the methyl group. Cr-ZSM- 5(240) demonstrated the highest hydrothermal stability due to its high Si/Al ratio. Despite giving a high initial activity due to its high metal loading, Cr-BEA(25) was susceptible to coking in the long run. The high coke formation in mordenite and beta zeolites was attributed to their high acidity, interconnecting channels of different sizes, and relatively larger pore sizes. The coke that formed on Cr-ZSM-5(240) was more carbonaceous and oxidized at higher temperatures.

scholarly journals Kinetika Reaksi Hidrogenasi Ester Lemak Menjadi Alkohol Lemak Dengan Katalis Tembaga- Mangan

2020 ◽  
Vol 8 (1) ◽  
pp. 21-27
Author(s):  
Melia Laniwati Gunawan ◽  
IGBN Makertihartha ◽  
Subagjo Subagjo
Keyword(s):  
Kinetic Equation ◽  
Fixed Bed ◽  
Acid Methyl Ester ◽  
Space Velocity ◽  
Lauryl Alcohol ◽  
Fixed Bed Reactor ◽  
Commercial Catalyst ◽  
Copper Manganese ◽  
High Pressure Reaction ◽  
Copper Based Catalyst

Fatty alcohol (FAOH) can be produced by hydrogenating of fatty acid methyl ester (FAME) using the copper-based catalyst. Copper-Chrom (Cu-Cr) is the best catalyst for high-pressure reaction condition, which is copper (Cu) as the main active component and chrom (Cr) as a promoter. Since Cr is feared to be toxic, one of the best replacement candidates is manganese (Mn). The research aims is to find the kinetic equation of hydrogenation FAME to FAOH using a Cu-Mn commercial catalyst.  FAME with methyl laurate and methyl myristate as the main compounds is used as feedstock. The main products are lauryl alcohol and myristyl alcohol. The reaction was carried out in an isothermal continuous fixed bed reactor under conditions of temperature 220 – 240 oC, pressure 50 bar, and liquid hourly space velocity (LHSV) 5-12.5 hr-1.  The kinetic equation is determined using the power law model. The FAME hydrogenation on copper - manganese catalyst is the half order reaction. The activation energy value is 86.32 kJ/mol and the Arrhenius constant value is 5.87x106  M0.5/s.

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