Ultra-High Surface Area Activated Porous Asphalt for CO2Capture through Competitive Adsorption at High Pressures

2016 ◽  
Vol 7 (1) ◽  
pp. 1600693 ◽  
Author(s):  
Almaz S. Jalilov ◽  
Yilun Li ◽  
Jian Tian ◽  
James M. Tour
2011 ◽  
Vol 1334 ◽  
Author(s):  
Tyler G. Voskuilen ◽  
Timothée L. Pourpoint

ABSTRACTAn experimental study of hydrogen adsorption in a variety of high-surface area adsorbent materials has been conducted at room temperature and pressures up to 500 bar on high surface area activated carbons, zeolite templated carbons (ZTC), and metal organic frameworks (MOFs). For all materials, excess hydrogen adsorption isotherms were measured up to 500 bar and have been analyzed in terms of the BET surface area and pore size distribution. The materials were also evaluated for their increase in hydrogen storage density over compressed gas. It was determined that, due to the lower excess adsorption and skeletal densities for the microstructured materials, MOF-177 and ZTC have worse storage densities than compressed gas at most pressures, even when assuming a bed compaction factor of two, while the activated carbons offer marginal increases in storage density over the pressure range investigated.


2012 ◽  
Vol 576 ◽  
pp. 402-405
Author(s):  
H. Misran ◽  
F.A.M. Zini ◽  
Musdalilah Ahmad Salim ◽  
Ramesh Singh

Mesoporous γ-alumina with relatively high surface area of ca. 590 m2/g and pore size of ca. 2.0 nm to ca. 9.7 nm were successfully processed using facile and cost-effective method in the presence of renewable, low-cost templates. Controlled addition of water during the processing of the materials was found to control the rapid hydrolysis rate of alumina precursors resulting in mesoporous formation. In addition, these materials porosity was made up from framework porosity as well as textural porosity given rise from the aggregations of γ-alumina nanoparticulates. Regardless of the materials specific surface area value, the competitive adsorption amount of energy gas in 68 % humidity environment increased as relative crystallinity of the materials increased.


Author(s):  
Kailun Yang ◽  
Recep Kas ◽  
Wilson A. Smith

<p>This study evaluated the performance of the commonly used strong buffer electrolytes, i.e. phosphate buffers, during CO<sub>2</sub> electroreduction in neutral pH conditions by using in-situ surface enhanced infrared absorption spectroscopy (SEIRAS). Unfortunately, the buffers break down a lot faster than anticipated which has serious implications on many studies in the literature such as selectivity and kinetic analysis of the electrocatalysts. Increasing electrolyte concentration, surprisingly, did not extend the potential window of the phosphate buffers due to dramatic increase in hydrogen evolution reaction. Even high concentration phosphate buffers (1 M) break down within the potentials (-1 V vs RHE) where hydrocarbons are formed on copper electrodes. We have extended the discussion to high surface area electrodes by evaluating electrodes composed of copper nanowires. We would like highlight that it is not possible to cope with high local current densities on these high surface area electrodes by using high buffer capacity solutions and the CO<sub>2</sub> electrocatalysts are needed to be evaluated by casting thin nanoparticle films onto inert substrates as commonly employed in fuel cell reactions and up to now scarcely employed in CO<sub>2</sub> electroreduction. In addition, we underscore that normalization of the electrocatalytic activity to the electrochemical active surface area is not the ultimate solution due to concentration gradient along the catalyst layer.This will “underestimate” the activity of high surface electrocatalyst and the degree of underestimation will depend on the thickness, porosity and morphology of the catalyst layer. </p> <p> </p>


Nanoscale ◽  
2015 ◽  
Vol 7 (25) ◽  
pp. 10974-10981 ◽  
Author(s):  
Xiulin Yang ◽  
Ang-Yu Lu ◽  
Yihan Zhu ◽  
Shixiong Min ◽  
Mohamed Nejib Hedhili ◽  
...  

High surface area FeP nanosheets on a carbon cloth were prepared by gas phase phosphidation of electroplated FeOOH, which exhibit exceptionally high catalytic efficiency and stability for hydrogen generation.


Author(s):  
Sisir Maity ◽  
Dheeraj Kumar Singh ◽  
Divya Bhutani ◽  
Suchitra Prasad ◽  
Umesh V. Waghmare ◽  
...  

MethodsX ◽  
2021 ◽  
pp. 101464
Author(s):  
Yichen Wu ◽  
Nan Zhang ◽  
Charles-François de Lannoy

2021 ◽  
Author(s):  
Gurwinder Singh ◽  
Rohan Bahadur ◽  
Ajanya Maria Ruban ◽  
Jefrin Marykala Davidraj ◽  
Dawei Su ◽  
...  

Nanoporous biocarbons derived from waste biomass have created significant attention owing to their great potential for energy storage and conversion and water purification. However, the fabrication technology for these materials...


Molecules ◽  
2021 ◽  
Vol 26 (7) ◽  
pp. 1962
Author(s):  
Mahboubeh Nabavinia ◽  
Baishali Kanjilal ◽  
Noahiro Fujinuma ◽  
Amos Mugweru ◽  
Iman Noshadi

To address the issue of global warming and climate change issues, recent research efforts have highlighted opportunities for capturing and electrochemically converting carbon dioxide (CO2). Despite metal doped polymers receiving widespread attention in this respect, the structures hitherto reported lack in ease of synthesis with scale up feasibility. In this study, a series of mesoporous metal-doped polymers (MRFs) with tunable metal functionality and hierarchical porosity were successfully synthesized using a one-step copolymerization of resorcinol and formaldehyde with Polyethyleneimine (PEI) under solvothermal conditions. The effect of PEI and metal doping concentrations were observed on physical properties and adsorption results. The results confirmed the role of PEI on the mesoporosity of the polymer networks and high surface area in addition to enhanced CO2 capture capacity. The resulting Cobalt doped material shows excellent thermal stability and promising CO2 capture performance, with equilibrium adsorption of 2.3 mmol CO2/g at 0 °C and 1 bar for at a surface area 675.62 m2/g. This mesoporous polymer, with its ease of synthesis is a promising candidate for promising for CO2 capture and possible subsequent electrochemical conversion.


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