Methane/Carbon Dioxide Adsorption and Diffusion Performances at Different Mineral Compositions and Buried Depth Conditions

2021 ◽  
Vol 35 (19) ◽  
pp. 15567-15578
Author(s):  
Xuanyan Dai ◽  
Sen Tian ◽  
Yi He ◽  
Yiyu Lu ◽  
Guangjin Wang
2014 ◽  
Vol 40 (7-9) ◽  
pp. 618-633 ◽  
Author(s):  
Nethika S. Suraweera ◽  
Austin A. Albert ◽  
Michael E. Peretich ◽  
Joshua Abbott ◽  
James R. Humble ◽  
...  

2017 ◽  
Vol 491 ◽  
pp. 118-125 ◽  
Author(s):  
Pavee Pongsajanukul ◽  
Vudhichai Parasuk ◽  
Siegfried Fritzsche ◽  
Suttichai Assabumrungrat ◽  
Suwimol Wongsakulphasatch ◽  
...  

2018 ◽  
Author(s):  
Jaya Prakash Madda ◽  
Pilli Govindaiah ◽  
Sushant Kumar Jena ◽  
Sabbhavat Krishna ◽  
Rupak Kishor

<p>Covalent organic Imine polymers with intrinsic meso-porosity were synthesized by condensation reaction between 4,4-diamino diphenyl methane and (para/meta/ortho)-phthaladehyde. Even though these polymers were synthesized from precursors of bis-bis covalent link mode, the bulk materials were micrometer size particles with intrinsic mesoporous enables nitrogen as well as carbon dioxide adsorption in the void spaces. These polymers were showed stability up to 260<sup>o</sup> centigrade. Nitrogen gas adsorption capacity up to 250 cc/g in the ambient pressure was observed with type III adsorption characteristic nature. Carbon dioxide adsorption experiments reveal the possible terminal amine functional group to carbamate with CO<sub>2</sub> gas molecule to the polymers. One of the imine polymers, COP-3 showed more carbon dioxide sorption capacity and isosteric heat of adsorption (Q<sub>st</sub>) than COP-1 and COP-2 at 273 K even though COP-3 had lower porosity for nitrogen gas than COP-1 and COP-2. We explained the trends in gas adsorption capacities and Qst values as a consequence of the intra molecular interactions confirmed by Density Functional Theory computational experiments on small molecular fragments.</p>


Author(s):  
A Pertiwiningrum ◽  
R N Besari ◽  
M A Wuri ◽  
A W Harto ◽  
N A Fitriyanto ◽  
...  

2021 ◽  
Vol 4 (1) ◽  
Author(s):  
Bernadette R. Cladek ◽  
S. Michelle Everett ◽  
Marshall T. McDonnell ◽  
Matthew G. Tucker ◽  
David J. Keffer ◽  
...  

AbstractA vast source of methane is found in gas hydrate deposits, which form naturally dispersed throughout ocean sediments and arctic permafrost. Methane may be obtained from hydrates by exchange with hydrocarbon byproduct carbon dioxide. It is imperative for the development of safe methane extraction and carbon dioxide sequestration to understand how methane and carbon dioxide co-occupy the same hydrate structure. Pair distribution functions (PDFs) provide atomic-scale structural insight into intermolecular interactions in methane and carbon dioxide hydrates. We present experimental neutron PDFs of methane, carbon dioxide and mixed methane-carbon dioxide hydrates at 10 K analyzed with complementing classical molecular dynamics simulations and Reverse Monte Carlo fitting. Mixed hydrate, which forms during the exchange process, is more locally disordered than methane or carbon dioxide hydrates. The behavior of mixed gas species cannot be interpolated from properties of pure compounds, and PDF measurements provide important understanding of how the guest composition impacts overall order in the hydrate structure.


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