Ammonia Vapor Removal by Cu3(BTC)2 and Its Characterization by MAS NMR

被引:206
作者
Peterson, Gregory W. [1 ]
Wagner, George W. [1 ]
Balboa, Alex [1 ]
Mahle, John [1 ]
Sewell, Tara [1 ]
Karwacki, Christopher J. [1 ]
机构
[1] Edgewood Chem Biol Ctr, Aberdeen Proving Ground, MD 21010 USA
关键词
METAL-ORGANIC FRAMEWORKS; HYDROGEN ADSORPTION; COPPER(II) SALTS; COMPLEXES; DESIGN; SORPTION; SITES; SPECTROSCOPY; DERIVATIVES; STABILITY;
D O I
10.1021/jp902736z
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Adsorption equilibria and NMR experiments were performed to study the adsorption and interactions of ammonia with metal-organic framework HKUST-1, or Cu-3(BTC)(2) (BTC = 1,3,5-benzenetricarboxylate). Ammonia capacities determined from chemical breakthrough measurements show significantly higher uptake capacities than from adsorption alone, suggesting a stronger interaction involving a potential reaction with the Cu-3(BTC)(2) framework. Indeed, H-1 MAS NMR reveals that a major disruption of the relatively simple spectrum Of Cu-3(BTC)(2) occurs to generate a composite spectrum consistent with Cu(OH)(2) and (NH4)(3)BTC species under humid conditions-the anticipated products of a copper(II) carboxylate reacted with limited ammonia. These species are not detected under dry conditions; however, reaction stoichiometry combined with XRD results suggests the partial formation of an indeterminate diammine copper(II) complex with some residual Cu-3(BTC)(2) structure retained. Cu(II)-induced paramagnetic shifts exhibited by various species in H-1 and C-13 MAS NMR spectra are consistent with model compounds and previous literature. Although results show extensive ammonia capacity Of Cu-3(BTC)(2), much of the capacity is due to reaction with the structure itself, causing a permanent loss in porosity and structural integrity.
引用
收藏
页码:13906 / 13917
页数:12
相关论文
共 39 条
[1]   Tailored porous materials [J].
Barton, TJ ;
Bull, LM ;
Klemperer, WG ;
Loy, DA ;
McEnaney, B ;
Misono, M ;
Monson, PA ;
Pez, G ;
Scherer, GW ;
Vartuli, JC ;
Yaghi, OM .
CHEMISTRY OF MATERIALS, 1999, 11 (10) :2633-2656
[2]   1,4-Benzenedicarboxylate derivatives as links in the design of paddle-wheel units and metal-organic frameworks [J].
Braun, ME ;
Steffek, CD ;
Kim, J ;
Rasmussen, PG ;
Yaghi, OM .
CHEMICAL COMMUNICATIONS, 2001, (24) :2532-2533
[3]   Metal-organic frameworks with high capacity and selectivity for harmful gases [J].
Britt, David ;
Tranchemontagne, David ;
Yaghi, Omar M. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (33) :11623-11627
[4]   Cu2(ATC)•6H2O:: Design of open metal sites in porous metal-organic crystals (ATC:1,3,5,7-adamantane tetracarboxylate) [J].
Chen, BL ;
Eddaoudi, M ;
Reineke, TM ;
Kampf, JW ;
O'Keeffe, M ;
Yaghi, OM .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2000, 122 (46) :11559-11560
[5]   High H2 adsorption in a microporous metal-organic framework with open metal sites [J].
Chen, BL ;
Ockwig, NW ;
Millward, AR ;
Contreras, DS ;
Yaghi, OM .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2005, 44 (30) :4745-4749
[6]   A chemically functionalizable nanoporous material [Cu3(TMA)2(H2O)3]n [J].
Chui, SSY ;
Lo, SMF ;
Charmant, JPH ;
Orpen, AG ;
Williams, ID .
SCIENCE, 1999, 283 (5405) :1148-1150
[7]   Sulfate formation on SOx trapping materials studied by cu and SK-edge XAFS [J].
Dathe, H ;
Jentys, A ;
Lercher, JA .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2005, 7 (06) :1283-1292
[8]   Metal organic frameworks based on Cu2+ and benzene-1,3,5-tricarboxylate as host for SO2 trapping agents [J].
Dathe, H ;
Peringer, E ;
Roberts, V ;
Jentys, A ;
Lercher, JA .
COMPTES RENDUS CHIMIE, 2005, 8 (3-4) :753-763
[9]   STRUCTURAL RELATIONS IN COPPER OXYSALT MINERALS .1. STRUCTURAL HIERARCHY [J].
EBY, RK ;
HAWTHORNE, FC .
ACTA CRYSTALLOGRAPHICA SECTION B-STRUCTURAL SCIENCE, 1993, 49 :28-56
[10]   Highly porous and stable metal-organic frameworks: Structure design and sorption properties [J].
Eddaoudi, M ;
Li, HL ;
Yaghi, OM .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2000, 122 (07) :1391-1397