Detailed Information on Publication Record
2014
Synthesis of homogeneous silicophosphate xerogels by non-hydrolytic condensation reactions
STÝSKALÍK, Aleš, David ŠKODA, Zdeněk MORAVEC, JG ABBOTT, CE BARNES et. al.Basic information
Original name
Synthesis of homogeneous silicophosphate xerogels by non-hydrolytic condensation reactions
Authors
STÝSKALÍK, Aleš (203 Czech Republic, belonging to the institution), David ŠKODA (203 Czech Republic, belonging to the institution), Zdeněk MORAVEC (203 Czech Republic, belonging to the institution), JG ABBOTT (840 United States of America), CE BARNES (840 United States of America) and Jiří PINKAS (203 Czech Republic, guarantor, belonging to the institution)
Edition
MICROPOROUS AND MESOPOROUS MATERIALS, AMSTERDAM, ELSEVIER SCIENCE BV, 2014, 1387-1811
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
10402 Inorganic and nuclear chemistry
Country of publisher
Netherlands
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 3.453
RIV identification code
RIV/00216224:14740/14:00073904
Organization unit
Central European Institute of Technology
UT WoS
000340990200026
Keywords in English
Sol-Gel; Non-hydrolytic; Silicophosphate; Phosphosilicate; Xerogel
Tags
Tags
International impact, Reviewed
Změněno: 5/3/2018 21:27, prof. RNDr. Jiří Pinkas, Ph.D.
Abstract
V originále
A novel non-hydrolytic synthesis of silicophosphate xerogels and optimization of reaction conditions to obtain products with a high degree of condensation and a large specific surface area are presented. Homogeneous products with a high content of Si-O-P bonds and SiO6 moieties were synthesized by an ester elimination route at low temperature from silicon acetate, Si(OAc)(4), and tris(trimethylsilyl) phosphate, OP(OSiMe3)(3) (TTP). Depending on the reaction conditions (temperature, solvent, time) it was possible to control the degree of condensation (up to 85.7%) and porosity of amorphous xerogels (apparent surface areas from 230 to 568 m(2) g(-1)). The composition and morphology of the xerogels, volatile reaction byproducts, thermal transformations and surface modification with methanol were followed by elemental analysis, IR spectroscopy, thermal analysis TG-DSC, nitrogen adsorption, C-13, Si-29, and P-31 solid-state NMR spectroscopy, and powder XRD. (C) 2014 Elsevier Inc. All rights reserved.
Links
ED1.1.00/02.0068, research and development project |
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EE2.3.30.0037, research and development project |
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GAP207/11/0555, research and development project |
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LH11028, research and development project |
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