Md. Nordin, Nik Abdul Hadi and Ismail, Ahmad Fauzi and Mustafa, Azeman and Goh, Peisean S. and Rana, D. and Matsuura, Takeshi (2014) Aqueous room temperature synthesis of zeolitic imidazole framework 8 (ZIF-8) with various concentrations of triethylamine. RSC Advances, 4 (63). pp. 33292-33300. ISSN 2046-2069
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Official URL: http://dx.doi.org/10.1039/c4ra03593c
Abstract
In this study, a zeolitic imidazole framework (ZIF-8) was prepared, and physico-chemical characterizations were performed to investigate the influences of triethylamine (TEA) on the crystallinity, particle size, morphology, and defects of ZIF-8 synthesized via an aqueous room temperature approach with a relatively low molar ratio of ligands to metal salts. Increasing the concentration of TEA by raising the TEA/total molar ratio from 0.004 to 0.007 prompted the formation of pure phase ZIF-8, whereas a TEA/total molar ratio below 0.004 did not result in a yield of ZIF-8. The particle size of ZIF-8 decreased from approximately 288 to 133 nm with increasing TEA/total molar ratio, except at a TEA/total molar ratio of 0.007. However, an excessive TEA/total molar ratio alters the 2-MeIM chemistry, and partially forms hydroxylated 2-MeIM. Thus, this study shows that at relatively low molar ratios of ligands to metal salts, up to a maximum TEA/total molar ratio of 0.006, the TEA concentration plays an important role in assisting crystal formation and in controlling the particle size of ZIF-8. The proposed procedure enables pure phase nanoscale ZIF-8 to be synthesized with a high product yield and with minimal chemical usage
Item Type: | Article |
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Uncontrolled Keywords: | crystal formation, crystallinities, molar ratio, physico-chemical characterization, product yields, room temperature, room temperature synthesis, triethylamines |
Subjects: | T Technology > TN Mining engineering. Metallurgy |
Divisions: | Petroleum and Renewable Energy Engineering |
ID Code: | 51918 |
Deposited By: | Siti Nor Hashidah Zakaria |
Deposited On: | 01 Feb 2016 03:51 |
Last Modified: | 27 Aug 2018 03:41 |
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