Dry Reforming of Methane Using a Solar-Thermal Aerosol Flow Reactor

2004 ◽  
Vol 43 (18) ◽  
pp. 5489-5495 ◽  
Author(s):  
Jaimee K. Dahl ◽  
Alan W. Weimer ◽  
Allan Lewandowski ◽  
Carl Bingham ◽  
Fabian Bruetsch ◽  
...  
Membranes ◽  
2021 ◽  
Vol 11 (7) ◽  
pp. 518
Author(s):  
Cecilia Mateos-Pedrero ◽  
Miguel A. Soria ◽  
Antonio Guerrero-Ruíz ◽  
Inmaculada Rodríguez-Ramos

The external surface of a commercial porous stainless steel (PSS) was modified by either oxidation in air at varying temperatures (600, 700, and 800 °C) or coating with different oxides (SiO2, Al2O3, and ZrO2). Among them, PSS-ZrO2 appears as the most suitable carrier for the synthesis of the Pd membrane. A composite Pd membrane supported on the PSS-ZrO2 substrate was prepared by the electroless plating deposition method. Supported Ru catalysts were first evaluated for the low-temperature methane dry reforming (DRM) reaction in a continuous flow reactor (CR). Ru/ZrO2-La2O3 catalyst was found to be active and stable, so it was used in a membrane reactor (MR), which enhances the methane conversions above the equilibrium values. The influence of adding H2O to the feed of DRM was investigated over a Ru/ZrO2-La2O3 catalyst in the MR. Activity results are compared with those measured in a CR. The addition of H2O into the feed favors other reactions such as Water-Gas Shift (RWGS) and Steam Reforming (SR), which occur together with DRM, resulting in a dramatic decrease of CO2 conversion and CO production, but a marked increase of H2 yield.


Author(s):  
Jeffrey Wyss ◽  
Janna Martinek ◽  
Michael Kerins ◽  
Jaimee K Dahl ◽  
Alan Weimer ◽  
...  

A graphite fluid-wall aerosol flow reactor heated with concentrated sunlight has been developed over the past five years for the solar-thermal decarbonization of methane. The fluid-wall is provided by an inert or compatible gas that prevents contact of reactants and products of reaction with a graphite reaction tube. The reactor provides for a low thermal mass that is compatible with intermittent sunlight and the graphite construction allows rapid heating/cooling rates and ultra-high temperatures. The decarbonization of methane has been demonstrated at over 90% for residence times on the order of 10 milliseconds at a reactor wall temperature near 2000 K. The carbon black resulting from the dissociation of methane is nanosized, amorphous, and ash-free and can be used for industrial rubber production. The hydrogen can be supplied to a pipeline and used for chemical processing or to supply fuel cell vehicles.


2011 ◽  
Vol 394 (1-2) ◽  
pp. 257-265 ◽  
Author(s):  
Nicholas E. McGuire ◽  
Neal P. Sullivan ◽  
Olaf Deutschmann ◽  
Huayang Zhu ◽  
Robert J. Kee

2011 ◽  
Vol 20 (6) ◽  
pp. 568-576 ◽  
Author(s):  
Y Sun ◽  
T. Ritchie ◽  
S.S. Hla ◽  
S. McEvoy ◽  
W. Stein ◽  
...  

Author(s):  
Loc Cam Luu ◽  
Tri Nguyen ◽  
Cuong Tien Hoang ◽  
Tien Trong Nguyen ◽  
Minh Hoang Phan ◽  
...  

Effectively using CO2-containing natural gas is an urgent requirement in Vietnam. Therefore, producing hydrogen and syngas by dry reforming of methane (СН4+СО2 = 2Н2+2СО) has gained renewed interest in recent years. In this paper, Ni/α- Al2O3 and Ni-Mg/α-Al2O3 catalysts were prepared by impregnation. Physico-chemical characteristics of catalysts were investigated via nitrogen physisorption (BET), X-Ray Diffraction (XRD), Transmission Electron Microscopy (TEM), and Temperature Programmed Reduction (TPR) methods. The activities of catalysts in CO2 reforming of CH4 were studied in a micro-flow reactor in the temperature range 550 –800oC, and content of CH4 and CO2 of 3 % mol. It was found that the conversion of CH4 and CO2 remarkably increased with the increase of reaction temperature from 550 to 700oC, but increased inconsiderably when the temperature reached more than 700oC. The selectivities of CO and H2 reached over 91 %. The modification of Ni/α- Al2O3 catalyst with Mg led to reduce the NiO particle size forme the new ZnO-MgO solid solution and increase the reductivity of catalyst. These improve the activity, selectivity and stability of catalyst. At the reaction temperature of 700oC, the conversions of CH4 and CO2 on Ni-Mg/α-Al2O3 reached 88.5 % and 72.3 %, respectively. The activities of catalysts were stable for 30 hours of reaction. Moreover, the role of Mg in the resistance to the coke formation on the catalyst surface was clarified via the results of temperature programmed oxidation (TPO) of spent catalysts after running the reaction for 30 hours at 700oC


Energy ◽  
2004 ◽  
Vol 29 (5-6) ◽  
pp. 715-725 ◽  
Author(s):  
Jaimee K Dahl ◽  
Karen J Buechler ◽  
Ryan Finley ◽  
Timothy Stanislaus ◽  
Alan W Weimer ◽  
...  

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