TY  - CONF
SN  - 25550403
PB  - EDP Sciences
Y1  - 2021///
VL  - 287
UR  - https://www.scopus.com/inward/record.uri?eid=2-s2.0-85145467096&doi=10.1051%2fe3sconf%2f202128702005&partnerID=40&md5=9743da0772d37c03b7497ff75c5284d8
A1  - Ismail, M.
A1  - Bustam, M.A.
A1  - Kari, N.E.F.
AV  - none
TI  - Screening of gallate-based metal-organic frameworks for single-component CO2 and CH4 gas
ID  - scholars14731
N1  - cited By 3; Conference of 2021 International Conference on Process Engineering and Advanced Materials, ICPEAM2020 ; Conference Date: 13 July 2021 Through 15 July 2021; Conference Code:185461
N2  - Adsorption using porous adsorbents is widely applied in carbon dioxide (CO2) capture due to its potential energy saving with low operating cost. Metal-organic frameworks (MOFs) are preferable over conventional adsorbents as MOFs have tunable structure properties. Organic linkers from phytochemicalbased give a new idea in forming MOFs. Gallic acid is classified under phytochemicals can act as an alternative organic linker in a new family of hybrid framework materials due to low cost, low toxicity, easy availability and naturally abundant. Due to unique property of MOFs that can be tailored, screening using systematic tool is very important. Molecular modeling is proven to play a crucial role in providing an estimation on adsorption capacity, selectivity and adsorbent selection. Grand Canonical Monte Carlo (GCMC) method via Sorption module in Material Studio was performed to compute loading curves of CO2 and methane (CH4) in MOFs. Based on the simulation results, it shows that gallate-based MOFs can be a new promising adsorbent in CO2 capture as the predicted CO2 loading is significantly higher than CH4. The highest predicted CO2 adsorption capacity is achieved by Mg-gallate and the lowest is by Ag-gallate with 7.79 mmol/g and 6.35 mmol/g respectively. The applicability of gallic acid to act as an alternative linker is relevant for practical applications. © The Authors, published by EDP Sciences. This is an open access article distributed under the terms of the Creative Commons Attribution License 4.0 (http://creativecommons.org/licenses/by/4.0/)
ER  -