羧酸盐
吸附
化学
铜
氨
无机化学
打赌理论
X射线光电子能谱
金属
金属有机骨架
解吸
傅里叶变换红外光谱
核化学
化学工程
有机化学
工程类
作者
Ehsan Binaeian,Yuning Li,Habib‐Allah Tayebi,Daqiang Yuan
标识
DOI:10.1016/j.jhazmat.2021.125933
摘要
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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