Combined Role of Water and Surface Chemistry in Reactive Adsorption of Ammonia on Graphite Oxides

被引:40
作者
Seredych, Mykola [1 ]
Bandosz, Teresa J. [1 ]
机构
[1] CUNY, Dept Chem, New York, NY 10031 USA
关键词
ACTIVATED CARBONS; GRAPHENE LAYERS; ACIDITY; OXYGEN; COMPOSITES; REDUCTION; SERIES; FTIR;
D O I
10.1021/la9037217
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Graphite oxide synthesized using the Brodie method was tested for ammonia adsorption after two different levels of drying in dynamic conditions at the ambient temperature. Surface characterization before and alter exposure to ammonia was done using X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy, and potentiometric titration. On the surface of the initial materials, besides epoxy, hydroxyl, and carboxylic groups, various amounts of water within the interlayer space arc present. The results showed that ammonia is in within the interlayer space of graphite oxides. Water enhances the amount of ammonia adsorbed via the dissolution and promotes the dissociation of surface functional groups. This enhances formation of ammonium ions. On the other hand. water screens the accessibility of epoxy and -COOH groups for reactions with ammonia and thus limits the amount adsorbed. The retention of ammonia on a partially dried graphite oxide is enhanced not only owing to those reactions but also because of the formation of new adsorption centers as a result of an incorporation of ammonia to the graphene layers.
引用
收藏
页码:5491 / 5498
页数:8
相关论文
共 39 条
[21]   Atomic and Electronic Structure of Graphene-Oxide [J].
Mkhoyan, K. Andre ;
Contryman, Alexander W. ;
Silcox, John ;
Stewart, Derek A. ;
Eda, Goki ;
Mattevi, Cecilia ;
Miller, Steve ;
Chhowalla, Manish .
NANO LETTERS, 2009, 9 (03) :1058-1063
[22]   Iron oxide pillared graphite [J].
Morishige, K ;
Hamada, T .
LANGMUIR, 2005, 21 (14) :6277-6281
[23]   A NEW STRUCTURE MODEL OF GRAPHITE OXIDE [J].
NAKAJIMA, T ;
MABUCHI, A ;
HAGIWARA, R .
CARBON, 1988, 26 (03) :357-361
[24]   Spectroscopic characterization of hydroxyl groups in SAPO-40 .1. Study of the template-free samples and their interaction with ammonia [J].
Onida, B ;
Gabelica, Z ;
Lourenco, J ;
Garrone, E .
JOURNAL OF PHYSICAL CHEMISTRY, 1996, 100 (26) :11072-11079
[25]   MOF-Graphite Oxide Composites: Combining the Uniqueness of Graphene Layers and Metal-Organic Frameworks [J].
Petit, Camille ;
Bandosz, Teresa J. .
ADVANCED MATERIALS, 2009, 21 (46) :4753-+
[26]   Revisiting the chemistry of graphite oxides and its effect on ammonia adsorption [J].
Petit, Camille ;
Seredych, Mykola ;
Bandosz, Teresa J. .
JOURNAL OF MATERIALS CHEMISTRY, 2009, 19 (48) :9176-9185
[27]   Characterization and FTIR studies of MnOx-CeO2 catalyst for low-temperature selective catalytic reduction of NO with NH3 [J].
Qi, GS ;
Yang, RT .
JOURNAL OF PHYSICAL CHEMISTRY B, 2004, 108 (40) :15738-15747
[28]  
Ruess G., 1947, MONATSH CHEM, V76, P381, DOI [DOI 10.1007/BF00898987, DOI 10.1007/BF01517560]
[29]   Functionalized single graphene sheets derived from splitting graphite oxide [J].
Schniepp, HC ;
Li, JL ;
McAllister, MJ ;
Sai, H ;
Herrera-Alonso, M ;
Adamson, DH ;
Prud'homme, RK ;
Car, R ;
Saville, DA ;
Aksay, IA .
JOURNAL OF PHYSICAL CHEMISTRY B, 2006, 110 (17) :8535-8539
[30]   GRAPHITE OXIDE .6. STRUCTURE OF GRAPHITE OXIDE [J].
SCHOLZ, W ;
BOEHM, HP .
ZEITSCHRIFT FUR ANORGANISCHE UND ALLGEMEINE CHEMIE, 1969, 369 (3-6) :327-&