STÝSKALÍK, Aleš, David ŠKODA, Zdeněk MORAVEC, JG ABBOTT, CE BARNES and Jiří PINKAS. Synthesis of homogeneous silicophosphate xerogels by non-hydrolytic condensation reactions. MICROPOROUS AND MESOPOROUS MATERIALS. AMSTERDAM: ELSEVIER SCIENCE BV, 2014, vol. 197, OCTOBER 2014, p. 204-212. ISSN 1387-1811. Available from: https://dx.doi.org/10.1016/j.micromeso.2014.06.019.
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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
Original language English
Type of outcome Article in a journal
Field of Study 10402 Inorganic and nuclear chemistry
Country of publisher Netherlands
Confidentiality degree is not subject to a state or trade secret
WWW URL
Impact factor Impact factor: 3.453
RIV identification code RIV/00216224:14740/14:00073904
Organization unit Central European Institute of Technology
Doi http://dx.doi.org/10.1016/j.micromeso.2014.06.019
UT WoS 000340990200026
Keywords in English Sol-Gel; Non-hydrolytic; Silicophosphate; Phosphosilicate; Xerogel
Tags kontrola MP, podil, rivok
Tags International impact, Reviewed
Changed by Changed by: prof. RNDr. Jiří Pinkas, Ph.D., učo 627. Changed: 5/3/2018 21:27.
Abstract
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 projectName: CEITEC - central european institute of technology
EE2.3.30.0037, research and development projectName: Zaměstnáním nejlepších mladých vědců k rozvoji mezinárodní spolupráce
GAP207/11/0555, research and development projectName: Oxidy a fosforečnany kovů jako formy jaderného odpadu: studium sonochemického srážení, tepelných přeměn a rozpustnosti (Acronym: OPNW)
Investor: Czech Science Foundation
LH11028, research and development projectName: Nehydrolytické sol-gelové reakce pro přípravu křemičitanů a fosforečnanů s řízenou porozitou a funkčními skupinami na povrchu (Acronym: NHSGKNOX)
Investor: Ministry of Education, Youth and Sports of the CR
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