Aromatic polyamides as new precursors of nitrogen and oxygen-doped ordered mesoporous carbons

被引:53
作者
Sanchez-Sanchez, Angela [1 ]
Suarez-Garcia, Fabian [1 ]
Martinez-Alonso, Amelia [1 ]
Tascon, Juan M. D. [1 ]
机构
[1] INCAR CSIC, Inst Nacl Carbon, Oviedo 33080, Spain
关键词
CHEMICAL-VAPOR-DEPOSITION; NANOPOROUS CARBONS; POLYARAMID FIBERS; PYROLYSIS; TRANSFORMATIONS; MESOSTRUCTURE; ACTIVATION; SILICAS; STORAGE; PPTA;
D O I
10.1016/j.carbon.2013.12.080
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
Polyamides are used for the first time as precursors in the synthesis of nitrogen- and oxygen-doped ordered mesoporous carbons (OMCs) by applying two synthetic methods, named here as: (i) organic phase synthesis (infiltration in situ by Yamazaki reaction-based method) and (ii) solid-state thermal polymerization (liquid infiltration and thermal polymerization of the monomer into the porosity of the template). In both cases, 3-aminobenzoic acid (MABA) and SBA-15 mesoporous silica are used as precursor and template, respectively, and the infiltration takes place in one single step. In the first method, the infiltration process is accomplished in situ through Yamazaki reaction of the MABA; in the second one, the MABA monomer is introduced into the channels of the silica template by incipient wetness dissolved in a common and low polluting organic solvent. After carbonization at 900 degrees C and removal of the template, OMCs with very narrow pore size distributions and nitrogen and oxygen contents as large as similar to 6 and 6.4-11.5 wt.%, respectively, are obtained. This work opens a new way to prepare advanced carbon materials, due to the wide variety of polyamides that can be synthesized by applying the two proposed methods to a large number of both aliphatic and aromatic precursors. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:119 / 129
页数:11
相关论文
共 50 条
[1]  
[Anonymous], 1980, Infrared Characteristic Group Frequencies
[2]  
Beguin F, 2010, ADV MAT TECH SER, P1
[3]  
Bottani EJ, 2008, ADSORPTION BY CARBONS, P53, DOI 10.1016/B978-008044464-2.50007-9
[4]   Nitrogen in aramid-based activated carbon fibers by TPD, XPS and XANES [J].
Boudou, J. P. ;
Parent, Ph. ;
Suarez-Garcia, F. ;
Villar-Rodil, S. ;
Martinez-Alonso, A. ;
Tascon, J. M. D. .
CARBON, 2006, 44 (12) :2452-2462
[5]  
Briggs D., 1998, SURFACE ANAL POLYM X
[6]  
Burchell T. D., 1999, Carbon Materials for Advanced Technologies
[7]   Modification of the pyrolysis/carbonization of PPTA polymer by intermediate isothermal treatments [J].
Castro-Muniz, Alberto ;
Martinez-Alonso, Amelia ;
Tascon, Juan M. D. .
CARBON, 2008, 46 (07) :985-993
[8]   Activated carbon fibers with a high content of surface functional groups by phosphoric acid activation of PPTA [J].
Castro-Muniz, Alberto ;
Suarez-Garcia, Fabian ;
Martinez-Alonso, Amelia ;
Tascon, Juan M. D. .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 2011, 361 (01) :307-315
[9]   Chemical transformations resulting from pyrolysis and CO2 activation of Kevlar flocks [J].
Cuesta, A ;
MartinezAlonso, A ;
Tascon, JMD ;
Bradley, RH .
CARBON, 1997, 35 (07) :967-976
[10]   X-ray photoelectron spectroscopy reference data for identification of the C3N4 phase in carbon-nitrogen films [J].
Dementjev, AP ;
de Graaf, A ;
van de Sanden, MCM ;
Maslakov, KI ;
Naumkin, AV ;
Serov, AA .
DIAMOND AND RELATED MATERIALS, 2000, 9 (11) :1904-1907