Capture of toxic gases in MOFs: SO2, H2S, NH3 and NOx

被引:127
作者
Martinez-Ahumada, Eva [1 ]
Diaz-Ramirez, Mariana L. [2 ]
Velasquez-Hernandez, Miriam de J. [3 ]
Jancik, Vojtech [4 ,5 ]
Ibarra, Ilich A. [1 ]
机构
[1] Univ Nacl Autonoma Mexico, Inst Invest Mat, Lab Fisicoquim & Reactividad Superficies LaFReS, Circuito Exterior S-N, Mexico City 04510, DF, Mexico
[2] Mississippi State Univ, Dept Chem, Box 9573, Mississippi State, MS 39762 USA
[3] Graz Univ Technol, Inst Phys & Theoret Chem, A-8010 Graz, Austria
[4] Univ Nacl Autonoma Mexico, Inst Quim, Ciudad Univ, Mexico City, DF, Mexico
[5] UAEM UNAM, Ctr Conjunto Invest Quim Sustentable, Carr Toluca Atlacomulco Km 14-5, Toluca 50200, Estado De Mexic, Mexico
关键词
METAL-ORGANIC FRAMEWORKS; HYDROGEN-SULFIDE ADSORPTION; FLUE-GAS; REACTIVE ADSORPTION; SULFUR-DIOXIDE; SELECTIVE REMOVAL; LOW-TEMPERATURE; CARBON-DIOXIDE; HIGH-CAPACITY; POWER-PLANTS;
D O I
10.1039/d1sc01609a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
MOFs are promising candidates for the capture of toxic gases since their adsorption properties can be tuned as a function of the topology and chemical composition of the pores. Although the main drawback of MOFs is their vulnerability to these highly corrosive gases which can compromise their chemical stability, remarkable examples have demonstrated high chemical stability to SO2, H2S, NH3 and NOx. Understanding the role of different chemical functionalities, within the pores of MOFs, is the key for accomplishing superior captures of these toxic gases. Thus, the interactions of such functional groups (coordinatively unsaturated metal sites, mu-OH groups, defective sites and halogen groups) with these toxic molecules, not only determines the capture properties of MOFs, but also can provide a guideline for the desigh of new multi-functionalised MOF materials. Thus, this perspective aims to provide valuable information on the significant progress on this environmental-remediation field, which could inspire more investigators to provide more and novel research on such challenging task.
引用
收藏
页码:6772 / 6799
页数:28
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