(667a) CO2/H2O Sorption Behaviour of Nickel Nanowires Immobilized in Silica Aerogels for the CO2 Hydration Reaction | AIChE

(667a) CO2/H2O Sorption Behaviour of Nickel Nanowires Immobilized in Silica Aerogels for the CO2 Hydration Reaction

Authors 

Martis, V. - Presenter, Surface Measurement Systems
Hassan, K. T., Newcastle University
Wang, J. W., Newcastle University
Han, X., Newcastle University
Siller, L., Newcastle University
The rise of carbon dioxide (CO2) in atmosphere is a major factor responsible for increasing global surface temperature. A possible solution to mitigate climate change is CO2 capture, storage and utilization (CCSU). CCSU could be useful for controlling and moderating anthropogenic emissions of greenhouse gases.

Several technologies have been considered to remove CO2 from flue gas streams including absorption, adsorption, membrane separations and cryogenic distillations. Another promising CCSU technology is removing CO2 by using the CO2 hydration reaction (CHR) which works well in the presence of catalyst such as carbonic anhydrase (CA). Other promising catalysts are nickel nanoparticles (NiNPs) developed by Siller et al. (17-19) which have catalytic activity to accelerate CHR. They are also stable in water based environments. Their catalytic activity is affected by surface area, surface structure of different dimensionalities of nanomaterials. In this work we study immobilized nickel nanowires (NiNWs) as 1D nanomaterials in SiO2 aerogels as a heterogeneous catalyst for the CHR and compared them with NiNPs as 0D nanomaterials. Data for the differences in catalytic activities for CHR in a vapor phase when two different forms of nickel nanomaterials (NiNPs and NiNWs) are immobilized in silica aerogels will be presented. CO2/H2O co-sorption measurements were employed to study the catalytic activity. Vacuum Dynamic Vapor Sorption Analyzer (DVS Vacuum) was employed to study CO2/H2O adsorption-desorption kinetics and isotherms.

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