Synthesis of Cu-BTC Metal-Organic Framework for CO2 Capture via Solvent-free Method: Effect of Metal Precursor and Molar Ratio

Abstract The Cu-BTC (Copper-1,3,5-benzene tricarboxylate) is one of the representative metal organic frameworks (MOFs) that has shown outstanding performance for carbon dioxide (CO2) adsorption. However, its conventional synthesis duration is relatively long, and the process requires the addition of...

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Main Authors: Pui San Ho, Kok Chung Chong, Soon Onn Lai, Sze Sin Lee, Woei Jye Lau, Shih-Yuan Lu, Boon Seng Ooi
Format: Article
Language:English
Published: Springer 2022-09-01
Series:Aerosol and Air Quality Research
Subjects:
Online Access:https://doi.org/10.4209/aaqr.220235
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author Pui San Ho
Kok Chung Chong
Soon Onn Lai
Sze Sin Lee
Woei Jye Lau
Shih-Yuan Lu
Boon Seng Ooi
author_facet Pui San Ho
Kok Chung Chong
Soon Onn Lai
Sze Sin Lee
Woei Jye Lau
Shih-Yuan Lu
Boon Seng Ooi
author_sort Pui San Ho
collection DOAJ
description Abstract The Cu-BTC (Copper-1,3,5-benzene tricarboxylate) is one of the representative metal organic frameworks (MOFs) that has shown outstanding performance for carbon dioxide (CO2) adsorption. However, its conventional synthesis duration is relatively long, and the process requires the addition of bulk amounts of organic solvents. Herein, an enhanced solvent-free synthesis strategy was demonstrated in this work for the Cu-BTC synthesis. For this enhanced method, Cu-BTC was synthesized in 3 hours by mechanically grinding the mixture of copper (Cu) metal precursor and BTC organic linker without using solvent. The as-synthesized Cu-BTC samples were analyzed using various characterization techniques to examine and confirm their properties. The thermal stability result revealed that the self-synthesized Cu-BTC could sustain high temperature up to 290°C. Among the samples synthesized at different mole ratios, the Cu-BTC sample with the Cu to BTC mole ratio of 1.5:1 showed the highest BET surface area and the most significant pore volume of 1044 m2 g−1 and 0.62 cm3 g−1, respectively. Its CO2 adsorption capacity was comparable with those fabricated using the solvent-based method, i.e., 1.7 mmol g−1 at 30°C and 1 bar. The results also showed that the synthesized Cu-BTC exhibited regenerative ability up to five adsorption-desorption cycles.
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spelling doaj-art-5d7f9546d721478a93373cf2e1fa2ff92025-02-09T12:18:19ZengSpringerAerosol and Air Quality Research1680-85842071-14092022-09-01221211410.4209/aaqr.220235Synthesis of Cu-BTC Metal-Organic Framework for CO2 Capture via Solvent-free Method: Effect of Metal Precursor and Molar RatioPui San Ho0Kok Chung Chong1Soon Onn Lai2Sze Sin Lee3Woei Jye Lau4Shih-Yuan Lu5Boon Seng Ooi6Department of Chemical Engineering, Lee Kong Chian Faculty of Engineering and Science, Universiti Tunku Abdul Rahman (UTAR)Department of Chemical Engineering, Lee Kong Chian Faculty of Engineering and Science, Universiti Tunku Abdul Rahman (UTAR)Department of Chemical Engineering, Lee Kong Chian Faculty of Engineering and Science, Universiti Tunku Abdul Rahman (UTAR)Department of Chemical Engineering, Lee Kong Chian Faculty of Engineering and Science, Universiti Tunku Abdul Rahman (UTAR)Advanced Membrane Technology Research Centre (AMTEC), School of Chemical and Energy Engineering, Universiti Teknologi MalaysiaDepartment of Chemical Engineering, National Tsing Hua UniversitySchool of Chemical Engineering, Engineering Campus, Universiti Sains MalaysiaAbstract The Cu-BTC (Copper-1,3,5-benzene tricarboxylate) is one of the representative metal organic frameworks (MOFs) that has shown outstanding performance for carbon dioxide (CO2) adsorption. However, its conventional synthesis duration is relatively long, and the process requires the addition of bulk amounts of organic solvents. Herein, an enhanced solvent-free synthesis strategy was demonstrated in this work for the Cu-BTC synthesis. For this enhanced method, Cu-BTC was synthesized in 3 hours by mechanically grinding the mixture of copper (Cu) metal precursor and BTC organic linker without using solvent. The as-synthesized Cu-BTC samples were analyzed using various characterization techniques to examine and confirm their properties. The thermal stability result revealed that the self-synthesized Cu-BTC could sustain high temperature up to 290°C. Among the samples synthesized at different mole ratios, the Cu-BTC sample with the Cu to BTC mole ratio of 1.5:1 showed the highest BET surface area and the most significant pore volume of 1044 m2 g−1 and 0.62 cm3 g−1, respectively. Its CO2 adsorption capacity was comparable with those fabricated using the solvent-based method, i.e., 1.7 mmol g−1 at 30°C and 1 bar. The results also showed that the synthesized Cu-BTC exhibited regenerative ability up to five adsorption-desorption cycles.https://doi.org/10.4209/aaqr.220235Metal-organic frameworkCu-BTCSolvent-freeCarbon dioxideAdsorption
spellingShingle Pui San Ho
Kok Chung Chong
Soon Onn Lai
Sze Sin Lee
Woei Jye Lau
Shih-Yuan Lu
Boon Seng Ooi
Synthesis of Cu-BTC Metal-Organic Framework for CO2 Capture via Solvent-free Method: Effect of Metal Precursor and Molar Ratio
Aerosol and Air Quality Research
Metal-organic framework
Cu-BTC
Solvent-free
Carbon dioxide
Adsorption
title Synthesis of Cu-BTC Metal-Organic Framework for CO2 Capture via Solvent-free Method: Effect of Metal Precursor and Molar Ratio
title_full Synthesis of Cu-BTC Metal-Organic Framework for CO2 Capture via Solvent-free Method: Effect of Metal Precursor and Molar Ratio
title_fullStr Synthesis of Cu-BTC Metal-Organic Framework for CO2 Capture via Solvent-free Method: Effect of Metal Precursor and Molar Ratio
title_full_unstemmed Synthesis of Cu-BTC Metal-Organic Framework for CO2 Capture via Solvent-free Method: Effect of Metal Precursor and Molar Ratio
title_short Synthesis of Cu-BTC Metal-Organic Framework for CO2 Capture via Solvent-free Method: Effect of Metal Precursor and Molar Ratio
title_sort synthesis of cu btc metal organic framework for co2 capture via solvent free method effect of metal precursor and molar ratio
topic Metal-organic framework
Cu-BTC
Solvent-free
Carbon dioxide
Adsorption
url https://doi.org/10.4209/aaqr.220235
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