Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/5135
Title: CO2 Adsorption Studies of Hydrophobic Silica Sorbent Functionalized with Silicone Oil-Amine Blends under Low-Temperature Conditions
Authors: Angitha, F
Ragi, T M
Mohamed, P A
Ananthakumar, S
Keywords: nanosilica
hydrophobic sorbent
amines
CO2 adsorption
silicone oil blends
Issue Date: 11-Jun-2025
Publisher: American Chemical Society
Citation: ACS Applied Engineering Materials; 3(6):1905–1914
Abstract: CO2 uptake using multifunctional, porous solid sorbents has gained significant attention due to their high thermochemical stability and selectivity. In this study, hydrophilic nanosilica was functionalized with blends of silicone oil and amines to develop hydrophobic silica sorbents capable of adsorbing CO2 at low temperatures in the presence of moisture. The adsorption performance of these sorbents was evaluated at 35 and 40 °C using silicone oil blends containing monoethanolamine (MEA), diethanolamine (DEA), and triethanolamine (TEA). Among these, the sorbent prepared with MEA, a primary amine, demonstrated the highest CO2 adsorption capacity. Further enhancement was achieved by functionalizing silicone oil with aminopropyltrimethoxysilane (APTMS). The optimized silica sorbent, with a 1:1 APTMS-to-silicone oil ratio, exhibited a maximum adsorption capacity of 0.75 and 0.86 mmol/g at 35 and 40 °C, respectively, and a water contact angle of 134°, achieving an optimal balance between hydrophobicity and amine reactivity. Their enhanced adsorption capacity and structural resilience suggest applications where intermittent moisture exposure may occur, such as indoor air purification systems, industrial enclosures, and controlled environments like greenhouses or cabin spaces. The hydrophobic surface is expected to improve durability and minimize water interference in such applications.
URI: https://pubs.acs.org/doi/10.1021/acsaenm.5c00365
http://localhost:8080/xmlui/handle/123456789/5135
Appears in Collections:2025



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