scholarly journals Impact of Carbon Dioxide on the Non-Catalytic Thermal Decomposition of Methane

2021 ◽  
Vol 5 (1) ◽  
pp. 12
Author(s):  
Tobias Marquardt ◽  
Sebastian Wendt ◽  
Stephan Kabelac

Economically and ecologically, the thermal decomposition of methane is a promising process for large scale hydrogen production. In this experimental study, the non-catalytic decomposition of methane in the presence of small amounts of carbon dioxide was analyzed. At large scales, natural gas or biomethane are possible feedstocks for the thermal decomposition and can obtain up to 5% carbon dioxide. Gas recycling can increase the amount of secondary components even further. Experiments were conducted in a packed flow reactor at temperatures from 1250 to 1350 K. The residence time and the amounts of carbon dioxide and hydrogen in the feed were varied. A methane conversion of up to 55.4% and a carbon dioxide conversion of up to 44.1% were observed. At 1300K the hydrogen yield was 95% for a feed of methane diluted in nitrogen. If carbon dioxide was added to the feed at up to a tenth with regard to the amount of supplied methane, the hydrogen yield was reduced to 85%. Hydrogen in the feed decreases the reaction rate of the methane decomposition and increases the carbon dioxide conversion.

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.


2021 ◽  
Author(s):  
Amita Chaudhary ◽  
Ashok N Bhaskarwar

Abstract Concentration of carbon dioxide gas has accelerated from the last two decades which cause drastic changes in the climatic conditions. In industries, carbon capture plants use volatile organic solvent which causes many environmental threats. So, a low-cost green absorbent has been formulated with nontoxicity and high selectivity properties for absorbing carbon dioxide gas. This paper contains the synthesis process along with the structure confirmation using 1H NMR, 13C NMR, FT-IR, and mass spectroscopy. Density, viscosity, and diffusivity are measured at different ranges with standard instruments. The kinetic studies were also conducted in a standard predefined-interface stirred-cell reactor. The kinetic parameters were calculated at different parameters like agitation speeds, absorption temperature, initial concentrations of ionic liquid, and partial pressure of carbon dioxide. The reaction regime of carbon dioxide absorption is found to be in fast reaction kinetics with pseudo first order. The reaction rate and the activation energy of CO2 absorption are experimentally determined in the range of 299 K to 333K with different initial concentrations of ionic liquid (0.1-1.1 kmol/m3). The second order rate constant and activation energy of carbon dioxide absorption in the synthesized ionic liquid is found to be (6385.93 to 12632.01 m3 mol-1 s-1) and 16.61 kJ mol−1 respectively. This solvent has shown great potential to absorb CO2 at large scale.


2021 ◽  
Vol 17 (1) ◽  
pp. 1-12
Author(s):  
Gaukhar E. Ergazieva ◽  
Nursaya Makayeva ◽  
Zhanna Shaimerden ◽  
Sergiy O. Soloviev ◽  
Мoldir Telbayeva ◽  
...  

This article discusses the decomposition of methane in the temperature range 550–800 °C on low-percentage   monometallic (Ni/g-Al2O3, Co/g-Al2O3) and bimetallic (Ni-Co/g-Al2O3) catalysts. It is shown that the bimetallic catalyst is more active in the decomposition of methane to hydrogen than monometallic ones. At a reaction temperature of 600 °C, the highest methane conversion is 81%, and the highest hydrogen yield of 51% is formed on Ni-Co/g-Al2O3. A complex of physicochemical methods (Scanning Electron Microscope (SEM), X-ray Diffraction (XRD), Temperature Programmed Reduction (TPR-H2), etc.) established that the addition of cobalt oxide to the composition of Ni/g-Al2O3 leads to the formation of surface bimetallic Ni-Co alloys, while the dispersion of particles increases and the reducibility of the catalyst is facilitated, which provides an increase in the concentration of metal particles - active centers, which can be the reason for an increase in the catalytic properties of a bimetallic catalyst in comparison with monometallic ones. Copyright © 2021 by Authors, Published by BCREC Group. This is an open access article under the CC BY-SA License  (https://creativecommons.org/licenses/by-sa/4.0). 


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.


Sign in / Sign up

Export Citation Format

Share Document