Metal-Organic Frameworks for Air Purification of Toxic Chemicals

被引:834
作者
DeCoste, Jared B. [1 ]
Peterson, Gregory W. [2 ]
机构
[1] Leidos Inc, Gunpowder, MD 21010 USA
[2] US Army Res Dev & Engn Command, Edgewood Chem Biol Ctr, Aberdeen Proving Ground, MD 21010 USA
关键词
COORDINATIVELY UNSATURATED SITES; HYDROGEN-SULFIDE ADSORPTION; NITRIC-OXIDE ADSORPTION; CU-BTC; REACTIVE ADSORPTION; CARBON-MONOXIDE; XYLENE ISOMERS; ZIRCONIUM HYDROXIDE; ACID SITES; METALLORGANIC FRAMEWORK;
D O I
10.1021/cr4006473
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The shortcoming of pure activated carbons is that chemicals with weak intermolecular forces typically have weak physical interactions with the carbon surface and therefore require chemical reactivity for removal. Thus, early gas masks were large, bulky, and burdensome to ensure proper protection for the user. Over the past century, the gas mask has changed substantially many times focused on the purported threat of the day. To properly afford broad spectrum protection, activated carbons must be impregnated with a variety of compounds capable of both acidic and basic chemistries. Due to the proximity of complementary functionalities within the pores of carbons, these chemical groups will inherently interact with one another over time, reducing the efficacy of the material. Instead, covalently anchoring functional groups to the substrate may be advantageous, a property that can be imparted through crystal design of materials, such as metal-organic frameworks (MOF).
引用
收藏
页码:5695 / 5727
页数:33
相关论文
共 224 条
[1]   Pore size distribution analysis of activated carbons prepared from coconut shell using methane adsorption data [J].
Ahmadpour, A. ;
Okhovat, A. ;
Mahboub, M. J. Darabi .
JOURNAL OF PHYSICS AND CHEMISTRY OF SOLIDS, 2013, 74 (06) :886-891
[2]   Immobilizing Highly Catalytically Active Pt Nanoparticles inside the Pores of Metal-Organic Framework: A Double Solvents Approach [J].
Aijaz, Arshad ;
Karkamkar, Abhi ;
Choi, Young Joon ;
Tsumori, Nobuko ;
Roennebro, Ewa ;
Autrey, Tom ;
Shioyama, Hiroshi ;
Xu, Qiang .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2012, 134 (34) :13926-13929
[3]   Probing the Lewis acidity and catalytic activity of the metal-organic framework [Cu3(btc)2] (BTC = benzene-1,3,5-tricarboxylate) [J].
Alaerts, Luc ;
Seguin, Etienne ;
Poelman, Hilde ;
Thibault-Starzyk, Frederic ;
Jacobs, Pierre A. ;
De Vos, Dirk E. .
CHEMISTRY-A EUROPEAN JOURNAL, 2006, 12 (28) :7353-7363
[4]   Metal-organic frameworks for the storage and delivery of biologically active hydrogen sulfide [J].
Allan, Phoebe K. ;
Wheatley, Paul S. ;
Aldous, David ;
Mohideen, M. Infas ;
Tang, Chiu ;
Hriljac, Joseph A. ;
Megson, Ian L. ;
Chapman, Karena W. ;
De Weireld, Guy ;
Vaesen, Sebastian ;
Morris, Russell E. .
DALTON TRANSACTIONS, 2012, 41 (14) :4060-4066
[5]   In Situ Single-Crystal Diffraction Studies of the Structural Transition of Metal-Organic Framework Copper 5-Sulfoisophthalate, Cu-SIP-3 [J].
Allan, Phoebe K. ;
Xiao, Bo ;
Teat, Simon J. ;
Knight, Jason W. ;
Morris, Russell E. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2010, 132 (10) :3605-3611
[6]  
[Anonymous], 2007, NIOSH POKCET GUIDE C
[7]  
[Anonymous], 2009, 1 JPEOCBD US DEP DEF
[8]  
[Anonymous], 2008, MED ASPECTS CHEM WAR
[9]  
Appl M, 2011, ULLMANNS ENCY IND CH
[10]   Reactions of VX, GD, and HD with Zr(OH)4: Near Instantaneous Decontamination of VX [J].
Bandosz, Teresa J. ;
Laskoski, Matt ;
Mahle, John ;
Mogilevsky, Gregory ;
Peterson, Gregory W. ;
Rossin, Joseph A. ;
Wagner, George W. .
JOURNAL OF PHYSICAL CHEMISTRY C, 2012, 116 (21) :11606-11614