Tuning of Delicate Host-Guest Interactions in Hydrated MIL-53 and Functional Variants for Furfural Capture from Aqueous Solution

被引:26
作者
Cao, Na [1 ,3 ]
Wang, Honglei [2 ]
Ban, Yujie [1 ]
Wang, Yuecheng [1 ,3 ]
Yang, Kun [1 ,3 ]
Zhou, Yingwu [1 ,3 ]
Zhao, Meng [1 ,3 ]
Deng, Weiqiao [2 ]
Yang, Weishen [1 ,3 ]
机构
[1] Chinese Acad Sci, State Key Lab Catalysis, Dalian Inst Chem Phys, 457 Zhongshan Rd, Dalian 116023, Peoples R China
[2] Shandong Univ, Inst Mol Sci & Engn, Qingdao 266237, Peoples R China
[3] Univ Chinese Acad Sci, 19A Yuquan Rd, Beijing 100039, Peoples R China
基金
中国国家自然科学基金;
关键词
adsorption; furfural; host-guest interactions; metal-organic frameworks; separation; METAL-ORGANIC FRAMEWORKS; ADSORPTION; SEPARATION; CO2; PURIFICATION; MEMBRANES; SOLIDS;
D O I
10.1002/anie.202011678
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Capture of high-boiling-point furfural from diluted aqueous solution is a critical but challenging step in sustainable bio-refinery processes, but conventional separation methods such as distillation and liquid-liquid extraction requires prohibitive energy consumption. We report control over the microenvironment of hydrated MIL-53 and isoreticular variants with diversified functional terephthalic acid linkers for the purpose of preferential binding of furfural through delicate host-guest interactions. Methyl-bounded MIL-53 with improved binding energy in the hydrated form results in highly efficient capture ratio (ca. 98 %) in the extremely low concentration of furfural solution (0.5-3 wt %) and 100 % furfural specificity over xylose. The distinct hydrogen bonding sites and multiple Van de Wall interactions for furfural adsorption was testified by computational modeling. Furthermore, the recovery ratio of furfural reaches ca. 93 % in desorption.
引用
收藏
页码:1629 / 1634
页数:6
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