Please use this identifier to cite or link to this item: doi:10.22028/D291-24510
Title: Thermal decoloration kinetics of spirooxazines in Ormocer coatings prepared via sol-gel processing
Author(s): Hou, Lisong
Schmidt, Helmut K.
Language: English
Year of Publication: 1996
OPUS Source: Journal of materials science. - 31. 1996, 13, S. 3427-3434
SWD key words: Spirooxazine
Ormocer
Sol-Gel-Verfahren
Ethanol
DDC notations: 620 Engineering and machine engineering
Publikation type: Journal Article
Abstract: Two free and one silylated (silane-substituted) photochromic spirooxazines are doped into organically modified ceramics (Ormocer) coatings by sol-gel processing and the thermal decoloration kinetics of these coatings are investigated and compared with the corresponding ethanol solutions and PMMA coatings. The decoloration behaviour of the two free dyes (SO-1 and SO-2) in the Ormocer coatings is similar to that in ethanol solutions, obeying a first-order mechanism and possessing almost the same decoloration rates as in ethanol. This suggests that the dye molecules encapsulated within the pores of the solid matrix are as free as those in ethanol solutions. The silylated dye (SO-3) in the Ormocer coatings, however, exhibits a considerably lower decoloration rate than the corresponding free dye (SO-1) and evident deviation from the first-order mechanism. This indicates apparently that the degree of freedom of the dye molecules is reduced by the silylation. These results are discussed on the basis of solvent polarity, porous structure of the Ormocer coating, and the dye-to-matrix connectivity.
Link to this record: urn:nbn:de:bsz:291-scidok-28234
hdl:20.500.11880/24566
http://dx.doi.org/10.22028/D291-24510
Date of registration: 9-Apr-2010
Faculty: SE - Sonstige Einrichtungen
Department: SE - INM Leibniz-Institut für Neue Materialien
Collections:INM
SciDok - Der Wissenschaftsserver der Universität des Saarlandes

Files for this record:
File Description SizeFormat 
sm199610.pdf679,1 kBAdobe PDFView/Open


Items in SciDok are protected by copyright, with all rights reserved, unless otherwise indicated.