Carbon Catalyzed Methane Decomposition for Enhanced Solar Thermal Cracking

Author(s):  
Vidyasagar Shilapuram ◽  
Nesrin Ozalp

This study presents thermal decomposition of methane, laden with two activated charcoal samples, namely Fluka 05105 and Fluka 05120, which were used laden with methane in a vortex flow solar reactor and seeded in a tornado flow solar reactor. Previously, we presented our thermo gravimetric experiment results on the carbon-hydrogen reaction to show whether the injected carbon particles react with the formed hydrogen. In this work, we expanded our thermogravimetric analysis to study carbon-methane reaction at various concentrations of methane feed gas to study the favorable effect of carbon laden flow experiments for catalytic methane decomposition. Results were analyzed to discuss the threshold temperature, ultimate mass gain, average hydrogen production, amount of carbon formed, type of carbon sample, and concentration of methane in the feed gas. It is observed that average hydrogen production rate is increased with an increase in the methane volume fraction in the feed gas. Higher hydrogen and carbon production is observed when Fluka 05105 is used. For different partial pressures of methane, different ultimate mass gain is observed.

Author(s):  
Nesrin Ozalp ◽  
Vidyasagar Shilapuram

Carbon is not only a major product of the methane decomposition but also a catalyst for the heterogeneous methane decomposition reaction. It is highly desirable that the morphology and surface properties of the product carbon be controlled to maximize their catalytic effects. In this paper, we characterize the physical properties of two activated carbon samples by sizes, and crystallographic structures using scanning electron microscope, x-ray diffraction, particle size analyzer, and surface area measurement. The paper also includes high temperature thermogravimetric experiment results on the carbon–hydrogen reaction to show if the injected carbon particles reacts with the formed hydrogen, which has not been studied in solar thermal hydrocarbon decomposition before. Results show that carbon does not react with hydrogen to form methane or any other intermediate compounds up until 900°C, which explains the favorable effect of carbon laden flow experiments for catalytic methane decomposition at lower temperatures. These results will be used to identify the optimal operating conditions for our solar reactor.


2018 ◽  
Author(s):  
◽  
Ronald Wafula Musamali

Overdependence on fossil-based fuels and their effect on environment is a global concern by energy stake holders. Bulk of present day hydrogen comes from gasification of coal, steam reforming and partial oxidation of hydrocarbons. Steam reforming accounts for over 50% of world hydrogen production despite producing carbonaceous gases which are harmful to the environment and poisonous to both; proton exchange fuel cells and alkaline fuel cells. Natural gas is a preferred feed for hydrogen production, because it is abundantly available on earth. Catalytic decomposition of ammonia can produce clean hydrogen but ammonia itself is an air pollutant. Catalytic decomposition of methane into carbon and hydrogen is an attractive option to producing clean hydrogen because its products are carbon and hydrogen. In this work, five different catalysts comprising of varying quantities of nickel and lithium, supported on calcium oxide were synthesized by incipient wetness impregnation method and designated according to weight % as; 30%Ni/CaO, 37.5%Ni-12.5%Li/CaO, 25.0%Ni- 25.0%Li/CaO, 12.5%Ni-37.5%Li/CaO and 50%Li/CaO. The synthesized catalysts were characterized by (XRD, SEM, BET and TEM) and tested for methane decomposition. From the XRD patterns of the synthesized catalysts, distinct crystalline phases of CaO and NiO were positively identified in 50%Ni/CaO according to their reference JCPDS files. Introduction of Lithium hydroxides improved the crystalline structure of the Ni/CaO catalyst. SEM analyses of the catalyst material using Image-J software confirmed that all catalyst materials were nanoparticles ranging from 3.09-6.56nm. BET results confirmed that, all the catalysts are mesoporous with pore sizes ranging from 20.1nm to 45.3nm. Introduction of LiOH to Ni/CaO generates mesoporous structures by destructing the lattices of the CaO structure during the formation of Ni-Li/CaO species. Particle size distribution in TEM analyses revealed that, a higher nickel loading in the catalyst favours the formation of carbon nanotubes while higher lithium hydroxide loading favours the formation of carbon fibres (CF). Low yield of carbon fibres from methane decomposition on unsupported Ni catalyst in 50%Ni/CaO was attributed to the presence of large Ni particles with low index planes which were incapable of dissociating the unreactive methane molecule. The aim of this work was to synthesize a catalyst for use in decomposition of methane into carbon and hydrogen, that addresses drawbacks of traditional solid metal catalysts such as sintering and coking. From the experimental results, 37.5%Ni-12.5%Li/CaO catalyst recorded 65.7% methane conversion and 38.3%hydrogen yield while 50%Ni/CaO recorded the lowest methane conversion of 60.2% and a hydrogen yield of 35.7% at 650℃. Outstanding performance of the 37.5%Ni-12.5%Li/CaO catalyst is attributed to the incorporation of lithium hydroxide which provided more catalyst active sites and a molten environment for proper dispersion of the nickel metal. The solid 50%Ni/CaO catalyst readily deactivated due to coking unlike the supported molten 37.5%Ni-12.5%Li/CaO catalyst in which methane decomposition reaction took place by both surface reaction and chemisorption.


Author(s):  
Irene Lock Sow Mei ◽  
S.S.M. Lock ◽  
Dai-Viet N. Vo ◽  
Bawadi Abdullah

<p>Hydrogen production from the direct thermo-catalytic decomposition of methane is a promising alternative for clean fuel production. However, thermal decomposition of methane can hardly be of any practical and empirical interest in the industry unless highly efficient and effective catalysts, in terms of both catalytic activity and operational lifetime have been developed. In this study, the effect of palladium (Pd) as a promoter onto Ni supported on alumina catalyst has been investigated by using co-precipitation technique. The introduction of Pd promotes better catalytic activity, operational lifetime and thermal stability of the catalyst. As expected, highest methane conversion was achieved at reaction temperature of 800 °C while the bimetallic catalyst (1 wt.% Ni -1wt.% Pd/Al<sub>2</sub>O<sub>3</sub>) gave the highest methane conversion of 70% over 15 min of time-on-stream (TOS). Interestingly, the introduction of Pd as promoter onto Ni-based catalyst also has a positive effect on the operational lifetime and thermal stability of the catalyst as the methane conversion has improved significantly over 240 min of TOS. Copyright © 2016 BCREC GROUP. All rights reserved</p><p><em>Received: 21<sup>st</sup> January 2016; Revised: 6<sup>th</sup> February 2016; Accepted: 6<sup>th</sup> March 2016</em></p><p><strong>How to Cite:</strong> Mei, I.L.S., Lock, S.S.M., Vo, D.V.N., Abdullah, B. (2016). Thermo-Catalytic Methane Decomposition for Hydrogen Production: Effect of Palladium Promoter on Ni-based Catalysts. Bulletin of Chemical Reaction Engineering &amp; Catalysis, 11 (2): 191-199 (doi:10.9767/bcrec.11.2.550.191-199)</p><p><strong>Permalink/DOI:</strong> http://dx.doi.org/10.9767/bcrec.11.2.550.191-199</p>


RSC Advances ◽  
2020 ◽  
Vol 10 (67) ◽  
pp. 40882-40893
Author(s):  
Khalida Harun ◽  
Sushil Adhikari ◽  
Hossein Jahromi

Methane decomposition over a carbon supported Ru catalyst (Ru–AC) and activated biochar (AB) for hydrogen production.


2006 ◽  
Vol 510-511 ◽  
pp. 30-33 ◽  
Author(s):  
Ling Han ◽  
Tae Ki Lim ◽  
Young Jun Kim ◽  
Hyun Sik Hahm ◽  
Myung Soo Kim

Catalytic decomposition of methane is an environmentally attractive approach to CO2-free hydrogen production. The decomposition of methane over carbon nanofibers was carried out in a fixed bed flow reactor. The objectives of this study are to demonstrate the activity of carbon nanofibers for methane decomposition in comparison with that of carbon black and to investigate the nature of active sites in the carbon catalysts. The catalytic activities of different carbon catalysts were found in the following order: carbon nanofiber > HI-900L carbon black > N330 carbon black > non-catalyst. After investigating the surface area and mass of the carbon catalysts after methane decomposition, the nature of active sites was discused.


Author(s):  
Hikmet Ibrahimov ◽  
Sara Malikli ◽  
Zenfira Ibrahimova ◽  
Rahim Babali ◽  
Sevinc Aleskerova

Abstractγ-Al2O3 was synthesized by the Sol–gel method, Ni (NO3)2 was placed in the pores by the impregnation method, and Ni-γ-Al2O3 was obtained by pyrolysis in a hydrogen stream in a CVD device. By the method of chemical vapors phase deposition (CVD) on Ni-Al2O3 catalytic converter with decomposition of methane in the natural gas produced carbon nanotubes (CNT) (Chunduri et al. in Mater Express 4(3):235–241, 2014; Zhou et al. in Appl Catal B 208:44–59, 2017). The catalytic activity of the catalysts in methane decomposition was examined from 650 °C to 900 °C by the method of chemical vapors phase deposition (CVD), the yield of CNTs tends to increase with the growth at the ratio of natural gas supply to hydrogen. The specific surface increases with an increase of nickel content and can reach 265.5 m2/g for a sample of 2% Ni-A12O3 at 850 °C. Growth at the temperature of methane decomposition leads to reduction in its specific surface. It has been established that the use of the Ni-Cu/γ-Al2O3 catalytic system, in which copper acts as a stabilizing additive, makes it possible to double the maximum yield of the carbon product during the decomposition of natural gas.


2021 ◽  
Vol 7 (3) ◽  
pp. 50
Author(s):  
Emmi Välimäki ◽  
Lasse Yli-Varo ◽  
Henrik Romar ◽  
Ulla Lassi

The hydrogen economy will play a key role in future energy systems. Several thermal and catalytic methods for hydrogen production have been presented. In this review, methane thermocatalytic and thermal decomposition into hydrogen gas and solid carbon are considered. These processes, known as the thermal decomposition of methane (TDM) and thermocatalytic decomposition (TCD) of methane, respectively, appear to have the greatest potential for hydrogen production. In particular, the focus is on the different types and properties of carbons formed during the decomposition processes. The applications for carbons are also investigated.


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