scholarly journals Influence of Substrate Concentration on Kinetic Parameters of Ethanol Dehydration in MFI and CHA Zeolites and Relation of These Kinetic Parameters to Acid–Base Properties

Catalysts ◽  
2022 ◽  
Vol 12 (1) ◽  
pp. 51
Author(s):  
Pavel Čičmanec ◽  
Jiří Kotera ◽  
Jan Vaculík ◽  
Roman Bulánek
Keyword(s):  
Activation Energy ◽  
Kinetic Parameters ◽  
Catalyst Deactivation ◽  
Fixed Bed ◽  
Fixed Bed Reactor ◽  
Ethanol Dehydration ◽  
Acid Base ◽  
Diffusion Limitations ◽  
Zeolite Lattice ◽  
Base Properties

The catalytic activity of zeolites is often related to their acid–base properties. In this work, the relationship between the value of apparent activation energy of ethanol dehydration, measured in a fixed bed reactor and by means of a temperature-programmed surface reaction (TPSR) depending on the amount of ethanol in the zeolite lattice and the value of activation energy of H/D exchange as a measure of acid–base properties of MFI and CHA zeolites, was studied. Tests in a fixed bed reactor were unable to provide reliable reaction kinetics data due to internal diffusion limitations and rapid catalyst deactivation. Only the TPSR method was able to provide activation energy values comparable to the activation energy values obtained from the H/D exchange rate measurements. In addition, for CHA zeolite, it has been shown that the values of ethanol dehydration activation energies depend on the amount of ethanol in the CHA framework, and this effect can be attributed to the substrate clustering effects supporting the deprotonation of zeolite Brønsted centers.

Pyrolysis Characteristics and Kinetics of Cassava Residues

2014 ◽  
Vol 953-954 ◽  
pp. 325-329
Author(s):  
Jin Wei Jia ◽  
Di Yang ◽  
He Long Hui ◽  
Xing Min Fu ◽  
Lu Liu ◽  
...  
Keyword(s):  
Activation Energy ◽  
Kinetic Parameters ◽  
Fixed Bed ◽  
The Other ◽  
Fixed Bed Reactor ◽  
Biomass Feedstock ◽  
Pyrolysis Characteristics ◽  
Three Samples ◽  
Bio Oil ◽  
Kinetics Of

The aims of this work were to investigate the influence of feedstock properties of different part of cassava residues (cassava rhizome (CR), cassava stalk (CS) and cassava leaf (CL)) and operating temperatures on the pyrolysis characteristics and the kinetic parameters. Pyrolysis experiments of three selected biomass feedstock were conducted using a fixed-bed reactor. It was shown that the bio-oil yield of cassava stalk reached the maxima at 600°C, and the char yield reduced with the temperature, whereas the gas yield increased with temperature. The cassava rhizome presented higher thermochemical reactivity than the other samples. The activation energy of cassava stalks was 37.57 kJ / mol and that of cassava rhizome (39.42 kJ / mol) increased slightly. The activation energy of cassava leaf (22.85 kJ / mol) was lowest of the three samples.

scholarly journals Analysis and Model-Based Description of the Total Process of Periodic Deactivation and Regeneration of a VOx Catalyst for Selective Dehydrogenation of Propane

Catalysts ◽  
2020 ◽  
Vol 10 (12) ◽  
pp. 1374
Author(s):  
Andreas Brune ◽  
Andreas Seidel-Morgenstern ◽  
Christof Hamel
Keyword(s):  
Catalyst Deactivation ◽  
Process Development ◽  
Coke Formation ◽  
Fixed Bed ◽  
Reaction Network ◽  
Fixed Bed Reactor ◽  
Side Reactions ◽  
Model Based ◽  
Total Process

This study intends to provide insights into various aspects related to the reaction kinetics of the VOx catalyzed propane dehydrogenation including main and side reactions and, in particular, catalyst deactivation and regeneration, which can be hardly found in combination in current literature. To kinetically describe the complex reaction network, a reduced model was fitted to lab scale experiments performed in a fixed bed reactor. Additionally, thermogravimetric analysis (TGA) was applied to investigate the coking behavior of the catalyst under defined conditions considering propane and propene as precursors for coke formation. Propene was identified to be the main coke precursor, which agrees with results of experiments using a segmented fixed bed reactor (FBR). A mechanistic multilayer-monolayer coke growth model was developed to mathematically describe the catalyst coking. Samples from long-term deactivation experiments in an FBR were used for regeneration experiments with oxygen to gasify the coke deposits in a TGA. A power law approach was able to describe the regeneration behavior well. Finally, the results of periodic experiments consisting of several deactivation and regeneration cycles verified the long-term stability of the catalyst and confirmed the validity of the derived and parametrized kinetic models for deactivation and regeneration, which will allow model-based process development and optimization.

Correlation between the acid–base properties of the La2O3 catalyst and its methane reactivity

2016 ◽  
Vol 18 (24) ◽  
pp. 16509-16517 ◽  
Author(s):  
Changqing Chu ◽  
Yonghui Zhao ◽  
Shenggang Li ◽  
Yuhan Sun
Keyword(s):  
Activation Energy ◽  
Linear Relationship ◽  
Acid Base ◽  
Chemisorption Energy ◽  
Base Properties

The linear relationship between CH4 activation energy and CO2 chemisorption energy illuminates the high OCM activity of strongly basic La2O3 catalysts.

scholarly journals Hydrogen Generation from Catalytic Steam Reforming Bio-Oil Model Compound—Acetic Acid Employing Ni/attapulgite Catalysts Prepared with Different Preparation Methods

2016 ◽  
Author(s):  
Yishuang Wang ◽  
Mingqiang Chen ◽  
Tian Liang ◽  
Jie Yang ◽  
Zhonglian Yang ◽  
...  
Keyword(s):  
Acetic Acid ◽  
Steam Reforming ◽  
Catalyst Deactivation ◽  
Hydrogen Generation ◽  
Fixed Bed ◽  
Fixed Bed Reactor ◽  
Precipitation Method ◽  
Impregnation Method ◽  
Bio Oil ◽  
Catalytic Steam Reforming

In this research, catalytic steam reforming acetic acid derived from the aqueous portion of bio-oil for hydrogen production was investigated by using different Ni/ATC (Attapulgite Clay) catalysts prepared by precipitation, impregnation and mechanical blending methods. The fresh and reduced catalysts were characterized by XRD, N2 adsorption-desorption, TEM and H2-TPR. The comprehensive results demonstrated that the interaction between active metallic Ni and ATC carrier was significantly improved in Ni/ATC catalyst prepared by precipitation method, and in which the mean Ni particle size was the smallest (~13 nm) resulted in the highest metal dispersion (7.5%). The catalytic performance of the three catalysts was evaluated through the process of steam reforming of acetic acid in a fixed-bed reactor under atmospheric pressure at two different temperatures, such as 550 ℃ and 650 ℃. Results showed that the Ni/ATC (PM-N/ATC) prepared by precipitation method, achieved the highest H2 yield of ~82% and little lower acetic acid conversion efficiency of ~85% than that (~95%) of Ni/ATC (IM-NATC) prepared by impregnation method. In addition, the deactivation catalysts after reaction for 4 h were analyzed by XRD, TGA-DTG and TEM, which demonstrated that the catalyst deactivation was not caused by the amount of carbon deposition, but owed to the significant agglomeration and sintering of Ni particles in the carrier.

Optimal catalyst activity distribution in fixed-bed reactor with catalyst deactivation

1989 ◽  
Vol 54 (2) ◽  
pp. 375-387 ◽  
Author(s):  
Jozef Markoš ◽  
Alena Brunovská
Keyword(s):  
Catalyst Deactivation ◽  
Active Catalyst ◽  
Catalyst Activity ◽  
Fixed Bed ◽  
Fixed Bed Reactor ◽  
Catalytic Reactor ◽  
Reactor Performance ◽  
Thiele Modulus ◽  
Activity Distribution ◽  
Parameter Ratio

In this paper the influence of the active catalyst location in a pellet on fixed-bed catalytic reactor performance is described. The optimal activity distribution as a function of an economic parameter (ratio of product and catalyst costs), Thiele modulus and Damkohler number is estimated.

Kinetic Modelling of Propane Dehydrogenation over a Pt–Sn/hierarchical SAPO-34 Zeolite Catalyst, Including Catalyst Deactivation

2017 ◽  
Vol 42 (4) ◽  
pp. 344-360
Author(s):  
Milad Komasi ◽  
Shohreh Fatemi ◽  
Seyed Hesam Mousavi
Keyword(s):  
Catalyst Deactivation ◽  
Kinetic Modelling ◽  
Coke Formation ◽  
Fixed Bed ◽  
Reaction Network ◽  
Normal Pressure ◽  
Fixed Bed Reactor ◽  
Propane Dehydrogenation ◽  
Coke Deposition ◽  
Formation Kinetic

Pt–Sn/hierarchical SAPO-34 was synthesised and kinetically modelled as an efficient and selective catalyst for propylene production through propane dehydrogenation. The kinetics of the reaction network were studied in an integral fixed-bed reactor at three temperatures of 550, 600 and 650 °C and weight hourly space velocities of 4 and 8 h−1 with a feed containing hydrogen and propane with relative molar ratios of 0.2, 0.5 and 0.8, at normal pressure. The experiments were performed in accordance with the full factorial experimental design. The kinetic models were constructed on the basis of different mechanisms and various deactivation models. The kinetics and deactivation parameters were simultaneously predicted and optimised using genetic algorithm optimisation. It was further proven that the Langmuir–Hinshelwood model can well predict propane dehydrogenation kinetics through lumping together all the possible dehydrogenation steps and also by assuming the surface reaction as the rate-determining step. A coke formation kinetic model has also shown appropriate results, confirming the experimental data by equal consideration of both monolayer and multilayer coke deposition kinetic orders and an exponential deactivation model.

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