scholarly journals A Simulation of the Tubular Packed Bed Reactor for the Steam-CO2Reforming of Natural Gas

2012 ◽  
Vol 23 (1) ◽  
pp. 73-82 ◽  
Author(s):  
Deuk-Ki Lee ◽  
Kee-Young Koo ◽  
Dong-Joo Seo ◽  
Wang-Lai Yoon
REAKTOR ◽  
2017 ◽  
Vol 7 (1) ◽  
pp. 7
Author(s):  
D. D. Anggoro

Methane is the main component of natural gas and this research provides the platrorm on the potential of utilizing natural gas, found abundant in Indonesia, to form gasoline. The objectives of the research are to modify HZSM-5 zeolite with a series of transition metals (Cr, Mn, Co, Ni, Cu, and Pt) and Ga , and to evaluate the performances  of these catalyst  for the single step conversion of methane to gasoline. The oxidation of methane were carried out in a micro-packed bed reactor at atmoepheric pressure, temperature 800 0C, F/W = 10440 ml/g.hr and 9%vol O2. Metals were loaded into the HZSM-5 zeolite by the wetness incipient impregnation method. The characterization results indicated that the ionic metals (Mn+) occupy the H+ position of HZSM-5 and metal loaded HZSM-5. Ni- HZSM-5, Cu- HZSM-5 and Ga- HZSM-5 gave a high methane conversion and high gasoline selectivity. Among the catalyst samles tested, Cr- HZSM-5 showed the highest  Research Octane Number (RON=86). These  catalyst have the potential  to convert natural gas to C5+ liquid hydrocarbons provided the oxidation, dehydration and oligomerization function of the metals are in balance.Keywords : direct conversion, methane, liquid hydrocarbons, metal, HZSM-5


2018 ◽  
Vol 33 (3) ◽  
pp. 1713-1721 ◽  
Author(s):  
Chenxia Xie ◽  
Yuning Dong ◽  
Liangliang Zhang ◽  
Guangwen Chu ◽  
Yong Luo ◽  
...  

2016 ◽  
Vol 192 ◽  
pp. 529-544 ◽  
Author(s):  
R. A. Hubble ◽  
J. Y. Lim ◽  
J. S. Dennis

The production of methane by reacting CO2 with H2 (CO2 methanation) has the potential for producing synthetic natural gas, which could be exported using the existing infrastructure for the distribution of natural gas. The methanation of CO2 was investigated over a wide range of partial pressures of products and reactants using (i) a gradientless, spinning-basket reactor operated in batch mode and (ii) a laboratory-scale packed bed reactor operated continuously. The rate and selectivity of CO2 methanation, using a 12 wt% Ni/γ-Al2O3 catalyst, were explored at temperatures 445–497 K and pressures up to 20 bar. Research with the batch reactor showed that the rate increased with increasing partial pressures of H2 and CO2 when the partial pressures of these reactants were low; however, the rate of reaction was found to be insensitive to changes in the partial pressures of H2 and CO2 when their partial pressures were high. A convenient method of determining the effect of H2O on the rate of reaction was also developed using the batch reactor and the inhibitory effect of H2O on CO2 methanation was quantified. The kinetic measurements were compared with a mathematical model of the reactor, in which different kinetic expressions were explored. The kinetics of the reaction were found to be consistent with a mechanism in which adsorbed CO2 dissociated to adsorbed CO and O on the surface of the catalyst with the rate-limiting step being the subsequent dissociation of adsorbed CO. The ability of the kinetic expressions to predict the results from the continuous, packed-bed reactor was explored, with some discrepancies discussed.


2021 ◽  
Vol 407 ◽  
pp. 127065
Author(s):  
Robert D. Franklin ◽  
Joshua A. Whitley ◽  
Adam A. Caparco ◽  
Bettina R. Bommarius ◽  
Julie A. Champion ◽  
...  

2017 ◽  
Vol 224 ◽  
pp. 292-297 ◽  
Author(s):  
Juntao Xu ◽  
Changsheng Liu ◽  
Meng Wang ◽  
Lei Shao ◽  
Li Deng ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document