Preparation and characterization of RGO-incorporated hypercross-linked polymers for CO2 capture

The growing demand for nano-structured composite materials and sustainable processes for next generation CO 2 capture technologies has necessitated the need to develop novel and cost-effective synthetic routes for solid CO 2 adsorbents based on hypercross-linked polymers (HCPs) and reduced graphene...

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Published inCarbon Letters Vol. 29; no. 1; pp. 21 - 30
Main Authors Vinodh, Rajangam, Babu, Cadiam Mohan, Abidov, Aziz, Palanichamy, Muthiahpillai, Cha, Wang Seog, Jang, Hyun Tae
Format Journal Article
LanguageEnglish
Published Singapore Springer Singapore 01.02.2019
Springer Nature B.V
한국탄소학회
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Summary:The growing demand for nano-structured composite materials and sustainable processes for next generation CO 2 capture technologies has necessitated the need to develop novel and cost-effective synthetic routes for solid CO 2 adsorbents based on hypercross-linked polymers (HCPs) and reduced graphene oxide (RGO) microporous sorbent materials with improved physico-chemical properties. The most important selection is modification of the synthesized microporous sorbent materials by the incorporation of RGO, giving rise to composite materials that combine the properties of both. These hybrid materials will be of great potential for carbon capture and storage (CCS) applications, especially for post-combustion CO 2 capture, owing to the increase in CO 2 capturing efficiency and selectivity to CO 2 compared to other flue gases. Herein, we report a facile and effective approach for fabrication of HCPs-supported reduced graphene oxide composites. The microporous HCPs was synthesized using 4,4′-bis(chloromethyl)-1,1′-biphenyl monomer by Friedel–Crafts alkylation. The RGO was prepared by modified Hammers method. The as-synthesized composites were characterized by TEM, SEM, FTIR, TGA and N 2 adsorption–desorption isotherm. The HCP/RGO composite showed maximum CO 2 adsorption of 5.1 wt% than the HCPs alone at 40 °C and 1 atm.
ISSN:1976-4251
2233-4998
DOI:10.1007/s42823-019-00002-6