Enhancing toxic gas uptake performance of Zr-based MOF through uncoordinated carboxylate and copper insertion;
Ehsan Binaeian1, Yuning Li2, Habib-Allah Tayebi3
1Department of Chemical Engineering and Waterloo Institute for Nanotechnology (WIN), University of Waterloo, 200 University Avenue West, Waterloo, ON N2L 3G1, Canada; Department of Chemical Engineering, Qaemshahr Branch, Islamic Azad University, Qaemshahr, Iran; State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Science, Fuzhou 350002, China.
Abstract:
This study reports the development of a new type of Zr-based MOF by inserting copper and carboxylate into HCl modulated UiO-67 (UiO-67-vac) which gained higher surface area/vacant than UiO-67. Copper was inserted into MOF containing uncoordinated carboxylate group, to create open metal site in the form of -COOCu which called UiO-67-ox-Cu. PXRD, FTIR, BET, SEM, EDS, UV-Vis and XPS were used to characterize the obtained MOFs. As expected, UiO-67-ox-Cu exhibits the highest ammonia capacity (178.3 mg/g) among UiO-67 (104 mg/g) and UiO-67-vac (121 mg/g) at 298 K and 1 bar pressure. In fact, the significant increase in ammonia uptake of UiO-67-ox-Cu is related to the modified binding affinity of -COOCu groups with ammonia. Moreover, UiO-67-vac with the highest surface area showed the hydrogen adsorption capacity of 18.75 mg/g at 77 K, which is comparable or even superior to the previously reported value. Interestingly, adsorption capacities were retained with slight changes around five cycles and three regeneration temperatures, 25, 60 and 120 °C under vacuum pressure which were proved by PXRD after ammonia adsorption/desorption. The good results obtained in the current work clearly show the role of postsynthesis functionalization approach for creation of new metal/active sites into MOFs.
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