scholarly journals D2 and H2 adsorption capacity and selectivity in CHA zeolites: Effect of Si/Al ratio, cationic composition and temperature

2020 ◽  
Vol 302 ◽  
pp. 110217 ◽  
Author(s):  
Igor Bezverkhyy ◽  
Quentin Pujol ◽  
Celine Dirand ◽  
Frédéric Herbst ◽  
Mathieu Macaud ◽  
...  
2018 ◽  
Vol 69 (6) ◽  
pp. 1468-1472
Author(s):  
Radu Mirea ◽  
Mihai Iordoc ◽  
Gabriela Oprina ◽  
Gimi Rimbu

The paper aims to present the investigation of H2 adsorption capacity in metal doped nanostructured materials, by using two methods. Carbonic materials are considered to be one of the most promising materials to be used for hydrogen adsorption and storage. They have different applications and one of the most important is considered to be fuel cells technology. By using metals for doping these materials, the adsorption capacity increases, thus approaching the target of 6.5% weight ratio of H2 adsorbed in a substrate. Within these investigations multi-wall nanotubes and poly-aniline have been used as substrates. The poly-aniline has been prepared and doped in laboratory while the nanotubes used in experiments have been purchased from the market and afterwards doped in laboratory. The doping procedure consists of a physical-chemical method which involves salts of the metal for doping and the use of ultrasounds in order to activate the substrate for doping. The adsorption capacity of the carbonic materials has been determined by using spill over phenomena in a PCT Pro-User apparatus, provided by SETARAM and also by cyclic voltametry, by using VoltaLab-40 apparatus. In order to investigate the adsorption capacity of the nanostructured carbonic materials, the experiments have been carried out at different pressures. Both substrates have been characterized in order to determine their porosity, BET surface and structure. The collected data have been processed by using the PCT Pro-User apparatus�s software. The results have been compared with the available data from literature and a good consistency was found.


CrystEngComm ◽  
2013 ◽  
Vol 15 (45) ◽  
pp. 9348 ◽  
Author(s):  
Zhiyong Lu ◽  
Liting Du ◽  
Baishu Zheng ◽  
Junfeng Bai ◽  
Mingxing Zhang ◽  
...  

2018 ◽  
Vol 270 ◽  
pp. 211-219 ◽  
Author(s):  
Maxence Giraudet ◽  
Igor Bezverkhyy ◽  
Guy Weber ◽  
Celine Dirand ◽  
Mathieu Macaud ◽  
...  

2009 ◽  
Vol 113 (16) ◽  
pp. 6839-6844 ◽  
Author(s):  
Mahasweta Nandi ◽  
Mohona Sarkar ◽  
Krishanu Sarkar ◽  
Asim Bhaumik

NANO ◽  
2017 ◽  
Vol 12 (01) ◽  
pp. 1750007 ◽  
Author(s):  
Weigang Zhao ◽  
Lu Luo ◽  
Mizi Fan

New monolithic nitrogen-containing microporous cellular activated carbon was successfully prepared from phenol-urea-formaldehyde (PUF) organic foam for CO2 and H2 adsorption and was characterized by thermogravimetric analysis (TG), scanning electron microscope (SEM), Fourier transform infrared spectroscopy (FTIR), elemental analysis (EA), a mechanical testing machine, N2-sorption and H2/CO2 sorption. The carbon yield was approximately 50% for carbonization and the burn off for activation ranged from 40% to 56%, which linearly increased with activation time. The macroporosity corresponded to the connected network of cells with diameters ranging from 100[Formula: see text][Formula: see text]m to 600[Formula: see text][Formula: see text]m, and the pinholes in the cell walls had diameters ranging from 1[Formula: see text][Formula: see text]m to 2[Formula: see text][Formula: see text]m. The micro/mesoporosity is located at the inner surface of the cells. Thus, higher adsorption kinetics than usual from activated carbon are expected. The developed carbon with the highest [Formula: see text] (1674 m2/g) and highest [Formula: see text] (0.86[Formula: see text]cm3/g) contained 1.5% nitrogen, had a CO2 adsorption capacity of 3.53[Formula: see text]mmol/g at 298[Formula: see text]K, and had an H2 adsorption capacity of 1.9[Formula: see text]wt.% at 77[Formula: see text]K, both at atmospheric pressure (1 bar), which were among the best in activated carbons from physical activation.


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>


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