scholarly journals Thermodynamic analysis on the CO2 conversion processes of methane dry reforming for hydrogen production and CO2 hydrogenation to dimethyl ether

Author(s):  
Xinyi He ◽  
Liping Liu
2015 ◽  
Vol 10 (4) ◽  
pp. 211-220 ◽  
Author(s):  
Bamidele V. Ayodele ◽  
Chin Kui Cheng

Abstract In this work, process modelling, thermodynamic analysis and optimization of stand-alone dry and partial oxidation reforming of methane as well as, the auto-thermal reforming processes were investigated. Firstly, flowsheet models were developed for both the stand-alone systems and auto-thermal reforming process using ASPEN HYSYS®. Furthermore, thermodynamic studies were conducted for the stand-alone and auto-thermal reforming processes for temperatures range of 200–1000°C and pressure range of 1–3 bar using Gibbs free energy minimization methods which was also performed using ASPEN HYSYS®. The simulation of the auto-thermal reforming process was also performed at 20 bar to mimic industrial process. Process parameters were optimized in the combined reforming process for hydrogen production using desirability function. The simulation results show that 84.60 kg/h, 62.08 kg/h and 154.7 kg/h of syngas were produced from 144 kg/h, 113 kg/h and 211 kg/h of the gas fed into the Gibbs reactor at CH4/CO2/O2 ratio 1:1:1 for the stand-alone dry reforming, partial oxidation reforming and auto-thermal processes respectively. Equilibrium conversion of CH4, CO2, O2 were thermodynamically favoured between 400 and 800°C with highest conversions of 100%, 95.9% and 86.7% for O2, CO2 and CH4 respectively. Highest yield of 99% for H2 and 40% for CO at 800°C was obtained. The optimum conditions for hydrogen production were obtained at CH4/CO2, CH4/O2 ratios of 0.634, 0.454 and temperature of 800°C respectively. The results obtained in this study corroborate experimental studies conducted on auto-thermal reforming of methane for hydrogen and syngas production.


2015 ◽  
Vol 2 ◽  
pp. 92-96 ◽  
Author(s):  
Z.Y. Zakaria ◽  
M. Jusoh ◽  
A. Johari ◽  
T.A. Tuan Abdullah ◽  
M.H. Hassim ◽  
...  

2014 ◽  
Vol 39 (30) ◽  
pp. 17009-17023 ◽  
Author(s):  
Muhammad Awais Naeem ◽  
Ahmed Sadeq Al-Fatesh ◽  
Anis Hamza Fakeeha ◽  
Ahmed Elhag Abasaeed

2014 ◽  
Vol 61 ◽  
pp. 2391-2394 ◽  
Author(s):  
Z.Y. Zakaria ◽  
M. Jusoh ◽  
A. Johari ◽  
M.A.A. Zaini ◽  
F.H. Kasim

Catalysts ◽  
2018 ◽  
Vol 8 (10) ◽  
pp. 481 ◽  
Author(s):  
Anand Kumar

Methane dry reforming (MDR) is an attractive alternative to methane steam reforming for hydrogen production with low harmful environmental emissions on account of utilizing carbon dioxide in the feed. However, carbon formation in the product stream has been the most challenging aspect of MDR, as it leads to catalyst deactivation by coking, prevalent in hydrocarbon reforming reactions. Common strategies to limit coking have mainly targeted catalyst modifications, such as by doping with rare earth metals, supporting on refractory oxides, adding oxygen/steam in the feed, or operating at reaction conditions (e.g., higher temperature), where carbon formation is thermodynamically restrained. These methods do help in suppressing carbon formation; nonetheless, to a large extent, catalyst activity and product selectivity are also adversely affected. In this study, the effect of ammonia addition in MDR feed on carbon suppression is presented. Based on a thermodynamic equilibrium analysis, the most significant observation of ammonia addition is towards low temperature carbon dioxide activation to methane, along with carbon removal. Results indicate that ammonia not only helps in removing carbon formation, but also greatly enriches hydrogen production.


Catalysts ◽  
2019 ◽  
Vol 10 (1) ◽  
pp. 21
Author(s):  
UPM Ashik ◽  
Shusaku Asano ◽  
Shinji Kudo ◽  
Doan Pham Minh ◽  
Srinivas Appari ◽  
...  

This study aimed to investigate the effect of carbon derived from glucose (C) on the physicochemical characteristics and catalytic activity of Ni, supported over SiO2, ZSM-5, and TiO2 in methane dry reforming. Among the Ni catalysts without C, Ni/SiO2 exhibited the highest CH4-CO2 conversion and stability at all experimented temperatures. On the other hand, the C-incorporated catalysts prepared by glucose impregnation, followed by pyrolysis, showed dissimilar performances. C improved the stability of Ni/SiO2 in the reforming at 650 °C and 750 °C and increased the CH4 and CO2 conversion to the level close to the thermodynamic equilibrium at 850 °C. However, this element did not substantially affect the activity of Ni/ZSM-5 and exerted a retarding effect on Ni/TiO2. Characterizations with H2-TPD, XRD, EXAFS, and STEM-EDS revealed that the different influences of C by the supports were attributed to the extent of metal dispersion and metal-support interaction.


2019 ◽  
Vol 44 (20) ◽  
pp. 9866-9872 ◽  
Author(s):  
Jiazheng Ren ◽  
Ming Li ◽  
Alex Chinghuan Lee ◽  
Kai Cheng ◽  
Yongsheng Chen

Sign in / Sign up

Export Citation Format

Share Document