Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/75790
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Type: Journal article
Title: Surface-functionalized periodic mesoporous organosilica hollow spheres
Author: Qiao, S.
Lin, C.
Jin, Y.
Li, Z.
Yan, Z.
Hao, Z.
Huang, Y.
Lu, G.
Citation: The Journal of Physical Chemistry C: Energy Conversion and Storage, Optical and Electronic Devices, Interfaces, Nanomaterials, and Hard Matter, 2009; 113(20):8673-8682
Publisher: American Chemical Society
Issue Date: 2009
ISSN: 1932-7447
1932-7455
Statement of
Responsibility: 
Shi Zhang Qiao, Chun Xiang Lin, Yonggang Jin, Zhen Li, Zhimin Yan, Zhengping Hao, Yining Huang and Gao Qing (Max) Lu
Abstract: Surface-functionalized periodic mesoporous organosilica (PMO) hollow spheres are successfully synthesized by using a hybrid silica precursor, l, 2-bis(trimethoxysilyl)ethane (BTME), and five precursors with different functional groups (-SH, -NH2, -CN, -C=C., -benzene) as well as surfactants, fluorocarbon and cetyltrimethylammoniuni bromide, combining a new vesicle and liquid crystal "dual templating" technique. Different disruption effects on the final mesostructure are observed following the order of-SH from 3-mercaptopropyltrimethoxysilane (MPTMS) > - benzene from (trimethoxysilyl)benzene (TMSB) - - C=C from vinyltrimethoxysilane (VTMS) > - NH2 from 3-aminopropyltriethoxysilane (APTES) > - CN from 3-cyanopropyltriethoxysilane (CPTES). The particle size, cavity size, and wall thickness of these hollow spheres can be adjusted by changing the amount of precursors or surfactants applied. In terms of providing better control over surface properties of products and giving more uniform surface coverage of functional groups, this direct synthesis method may benefit future production of hollow particles by a combination of various bridged organic and terminal functional groups for more versatile applications in catalyst, separation, drug/gene delivery, microelectronics field, etc. © 2009 American Chemical Society.
Rights: © 2009 American Chemical Society
DOI: 10.1021/jp810844p
Published version: http://dx.doi.org/10.1021/jp810844p
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