Ordered mesoporous ceramics stable up to 1500°C from diblock copolymer mesophases

被引:82
作者
Kamperman, M [1 ]
Garcia, CBW [1 ]
Du, P [1 ]
Ow, HS [1 ]
Wiesner, U [1 ]
机构
[1] Cornell Univ, Dept Mat Sci & Engn, Ithaca, NY 14853 USA
关键词
D O I
10.1021/ja046795h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In the present study, a poly(isoprene-block-dimethylamino ethyl methacrylate) diblock copolymer (PI-b-PDMAEMA) is used to structure-direct a polysilazane pre-ceramic polymer, commercially known as Ceraset. To the polymer was added a 2-fold excess in weight of the silazane oligomer (Ceraset). The resulting composite was cast into films, and after cooperative self-assembly of block copolymer and Ceraset, the structure was permanently set in the hexagonal columnar morphology, as evidenced by small-angle X-ray scattering (SAXS) and transmission electron microscopy (TEM). Cross-linking of the silazane oligomer was achieved with a radical initiator at 120 °C. Upon heating of the composite to 1500 °C under nitrogen, the structure is preserved and a mesoporous ceramic material is obtained, as demonstrated by SAXS and TEM. The pores are open and accessible, as evidenced by nitrogen sorption/desorption measurements indicating a surface area of about 51 m2 g-1 and a pore diameter of 13 nm, consistent with TEM analysis. These results suggest that the use of block copolymer mesophases may provide a simple, easily controlled pathway for the preparation of various high-temperature ceramic mesostructures. Copyright © 2004 American Chemical Society.
引用
收藏
页码:14708 / 14709
页数:2
相关论文
共 13 条
[1]   THE DETERMINATION OF PORE VOLUME AND AREA DISTRIBUTIONS IN POROUS SUBSTANCES .1. COMPUTATIONS FROM NITROGEN ISOTHERMS [J].
BARRETT, EP ;
JOYNER, LG ;
HALENDA, PP .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1951, 73 (01) :373-380
[2]   On a theory of the van der Waals adsorption of gases [J].
Brunauer, S ;
Deming, LS ;
Deming, WE ;
Teller, E .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1940, 62 :1723-1732
[3]   Living anionic homopolymerization and block copolymerization of (dimethylamino)ethyl methacrylate [J].
Creutz, S ;
Teyssie, P ;
Jerome, R .
MACROMOLECULES, 1997, 30 (01) :6-9
[4]   Synthesis and characterization of block copolymer/ceramic precursor nanocomposites based on a polysilazane [J].
Garcia, CBW ;
Lovell, C ;
Curry, C ;
Faught, M ;
Zhang, YM ;
Wiesner, U .
JOURNAL OF POLYMER SCIENCE PART B-POLYMER PHYSICS, 2003, 41 (24) :3346-3350
[5]   Mesoporous materials by templating of liquid crystalline phases [J].
Goltner, CG ;
Antonietti, M .
ADVANCED MATERIALS, 1997, 9 (05) :431-&
[6]  
Hamley I., 1998, The Physics of Block Copolymers Oxford University Press
[7]   ORDERED MESOPOROUS MOLECULAR-SIEVES SYNTHESIZED BY A LIQUID-CRYSTAL TEMPLATE MECHANISM [J].
KRESGE, CT ;
LEONOWICZ, ME ;
ROTH, WJ ;
VARTULI, JC ;
BECK, JS .
NATURE, 1992, 359 (6397) :710-712
[8]  
MATSUMOTO RLK, 1990, MATER RES SOC SYMP P, V180, P797, DOI 10.1557/PROC-180-797
[9]   Mechanical properties of a fully dense polymer derived ceramic made by a novel pressure casting process [J].
Shah, SR ;
Raj, R .
ACTA MATERIALIA, 2002, 50 (16) :4093-4103
[10]   Block copolymer-ceramic hybrid materials from organically modified ceramic precursors [J].
Simon, PFW ;
Ulrich, R ;
Spiess, HW ;
Wiesner, U .
CHEMISTRY OF MATERIALS, 2001, 13 (10) :3464-3486