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جستجوی مقالات مرتبط با کلیدواژه « kinetic study » در نشریات گروه « مهندسی شیمی، نفت و پلیمر »

تکرار جستجوی کلیدواژه «kinetic study» در نشریات گروه «فنی و مهندسی»
  • Mehrsa Emami *, Farzin Hormozi, Hossein Abedini
    Bulk phase polymerization of propylene with a 4th generation of Ziegler-Natta catalyst was kinetically investigated by means of heat flow calorimetry. The assumptions and modifications on isothermal calorimetric method were demonstrated. Our calibration method showed that heat exchange with the reactor cover plate is not constant over time. Therefore, the dynamic of cover plate temperature was considered in the calorimetric method. The polymerization rate profiles depending on hydrogen and external electron donor concentration have been investigated. Normalized polymerization profiles (Rp /Rpmax) are plotted and expressed as an exponential function of time. Effects of hydrogen and external electron donor (ED) concentration on Rpmax and polymerization rate were investigated as well. The results showed that by increasing hydrogen concentration, initial polymerization rate (Rpmax) increased. Hydrogen increased productivity by increasing the initial polymerization rate, while it had no negative effect on the rates of decay or its effect was small. The ED concentration was optimized so that the catalyst deactivation rate was at its lowest level. Also, changes in the ratio of activation to inactivation with ED concentration were examined, and a proportional change was observed.
    Keywords: kinetic study, calorimetry, liquid monomer, Propylene, polymerization}
  • Hamid Abbasi, Fariborz Rashidi*, Mohammad Mahdi Moshrefi
    Conventionally, methane is reformed into syngas, and subsequently converted into C1-oxygenates (methanol and formaldehyde). A novel option is the catalyst-free single-step conversion of methane to C1-oxygenates. This study presents a comprehensive model of methane partial oxidation to formaldehyde as an intermediate chemical species in methane oxidation process using microreactor. The dependency of C1-oxygenates yield on operating parameters is crucial. Therefore a representative mathematical model is constructed and solved in order to investigate the effect of operating temperature, feed flow-rate, and composition on the formaldehyde yield. Fifty-four coupled of differential equations are solved by finite element method. Moreover, to simulate the process, GRI-Mech 3.0 is employed as the reaction kinetics. A good agreement was achieved when the model results were compared with experimental data from the literature in terms of formaldehyde concentration and methane conversion. Finally, results of the study are presented and discussed on the basis of a major reaction pathway proposed in this study for methane oxidation at low temperature, and the important design criteria are presented. With respect to the model results, 5.5% yield for formaldehyde per one pass of microreactor was achieved at the operating condition of T = 1000 K and O2/CH4 ratio = 17.
    Keywords: Methane, Formaldehyde, Microreactor, Single Step, Non-catalytic, Kinetic Study}
  • علی صابری مقدم *، علی نوذری
    در این پژوهش فرآیند ریفرمینگ متان با بخار آب با کاتالیزور Ni-Al-Zn مورد بررسی قرار گرفت. این فرآیند در صنعت در محدوده دمایی 900oC-750 انجام می‎شود. به منظور کاهش دمای عملیاتی که از نظر اقتصادی و فرآیندی بسیار مهم است، کاتالیزور Ni-Al-Zn مورد بررسی قرار گرفت. این کاتالیزور از روش هم‎رسوبی ساخته شد. نتایج آنالیزهایXRD ، ICP و BET نحوه ساخت کاتالیست را تایید کردند. سپس این کاتالیست در فرآیند ریفرمینگ متان با بخار آب بررسی شد و مشخص گردید که درصد بهینه نیکل در کاتالیست 15% است. عملکرد این کاتالیزور در دمای 650oC شبیه کاتالیزور صنعتی در دمای 750oC در شرایط آزمایشگاهی است به‎طوری‎که در این دما، تبدیل متان نزدیک به 75% است. همچنین این کاتالیزور در دماهای بیش از 600oC نسبت به رسوب کربن مقاوم است. پس از ارزیابی کاتالیست، آزمایش‎های سینتیک روی آن صورت گرفت. انرژی فعال‎سازی برای واکنش تبدیل متان به CO و H2، واکنش تبدیل آب- گاز و تبدیل متان به CO2 و H به‎ترتیب kJ/mol 4/219، kJ/mol 90/71 و kJ/mol 04/221 به‎دست آمد. برای واکنش‎های تبدیل متان انرژی فعال‎سازی کمتر از مقادیر کاتالیزور صنعتی به‎دست آمد که نشان‎دهنده عملکرد مناسب کاتالیزور در این فرآیند است. همچنین پارامترهای مربوط به جذب گازها روی کاتالیست از نظر ترمودینامیکی مورد ارزیابی قرار گرفت و تایید شد.
    کلید واژگان: ریفرمینگ متان با بخار آب, کاتالیست Ni-Al-Zn, مطالعه سینتیک, تبدیل متان, انرژی فعال‎سازی}
    Ali Saberimoghaddam*, ALi Nozari
    In this study, steam methane reforming was investigated by using Ni-Al-Zn catalyst. This process carried out at 750-900 °C in the industrial plants. From the economical and operational point of view, the reduction of operational temperature is important. Therefore, the Ni-Al-Zn catalyst was studied to decrease the operational temperature. This catalyst was synthesized by coprecipitation method. The results of XRD, ICP, and BET revealed that catalyst were appropriately synthesized. Then, this catalyst was used in the steam methane reforming process and 15% nickel was obtained as optimum value. The performance of optimum catalyst at 650 °C was similar to industrial catalyst at 750 °C, so that the methane conversion was about 75 %. This catalyst showed high carbon resistance at temperatures above 600 °C. Kinetic study of optimum catalyst was performed. Moreover, the activation energy for reaction of methane to CO and H2, water gas shift and methane to CO2 and H2 were 219.4 kJ/mol, 71.90 kJ/mol, and 221.04 kJ/mol, respectively. The results of kinetic experiments on the synthesized catalyst showed that the activation energy for the first and third reactions of reforming (hydrogen production via methane and steam) was less than the activation energy on the industrial catalyst which reveals higher activity of the synthesized catalyst. Furthermore, the adsorption parameters in the kinetics equations were obtained and thermodynamically verified.
    Keywords: Steam Methane Reforming, Ni-Al-Zn Catalyst, Kinetic Study, Methane Conversion, Activation Energy}
  • N. Hadi, A. Niaei, S.R. Nabavi, A. Farzi
    A series of experiments were carried out by mixture of methanol and water as feed of the methanol to propylene (MTP) process in temperature range of 623-823 K. The H-ZSM5 catalyst with the Si/Al ratio of 200 was applied for carrying out the experiments. A novel lumped kinetic scheme was proposed for methanol to propylene (MTP) process. The reactor was mathematically modeled by assumptions of being isothermal, fixed bed, plug flow and the hybrid genetic algorithm was applied for estimating the kinetic parameters. The temperature dependency of the kinetic parameters was determined, using the modified Arrhenius relation. A good agreement was observed between the experimental and the calculated data. Effect of temperature on propylene and ethylene selectivity was investigated. It was found that the propylene selectivity increases with temperature until 773.15 K, but after that it decreases.
    Keywords: Kinetic Study, Methanol to Propylene Process, Lumped Mechanism, Hybrid Genetic Algorithm, High silica H, ZSM5 Nano Catalyst}
  • R. Alizadeh, E. Jamshidi, H. Ale Ebrahim, A. Afshar Ebrahimi
    This article describes kinetic modeling of the reduction of barium sulfate by methane based on experimental data obtained by thermogravimetric technique. The conversion-time data have been interpreted by using the grain model for gas-solid reactions and the effect of catalyst on the kinetic parameters has been elucidated. It was found that zinc oxide acted as a fairly strong catalyst for the reaction, especially at higher temperatures. For example, at about 950°C the reaction rate constant was increased more than 8 times by using only 2 percent of zinc oxide. Orthogonal collocation method was used for solving coupled partial differential equations of gas-solid reaction. There is a good agreement between the experimental data and results obtained from simulation. This research offers a clean method for barium carbonate production with methane as a reducing agent, decreasing CO2 emission significantly. Also, a new process for converting sulfur dioxide to elemental sulfur by a cyclic process involving barium sulfide and barium sulfate has been proposed.
    Keywords: Modeling, Barium Sulfate, Methane Reduction, Catalyst, Zinc Oxide, Kinetic Study}
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