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FT-IR and Raman spectroscopic study of di-urea cross-linked poly(oxyethylene)/siloxane ormolytes doped with Zn2+ ions

S. C. Nunes ; V. De Zea Bermudez ; Denis Ostrovskii (Institutionen för teknisk fysik) ; L. D. Carlos
Vibrational Spectroscopy (09242031 (ISSN)). Vol. 40 (2006), 2, p. 278-288.
[Artikel, refereegranskad vetenskaplig]

The interactions occurring in di-urea (NHC(O)NH) cross-linked poly(oxyethylene) (POE)/siloxane hybrids (di-ureasils) doped with zinc triflate (Zn(CF3SO3)2) were investigated by Fourier Transform infrared (FT-IR) and Raman (FT-Raman) spectroscopies. Bonding of the Zn2+ ions to the urea carbonyl oxygen atoms occurs in the entire range of compositions studied (∞ > n ≥ 1, where n, salt content, is the molar ratio of oxyethylene moieties per Zn2+ ion). At n > 20 the incorporation of the guest cations progressively reduces the number of free CO groups. At n = 20 the saturation of the urea cross-links is attained and the Zn2+ ions start to coordinate to the POE chains giving rise to the formation of a crystalline POE/Zn(CF3SO3)2 complex. The latter process occurs at the expense of the destruction of the hydrogen-bonded POE/urea structures of the host di-ureasil structure. New hydrogen-bonded associations, more ordered than the urea-urea aggregates present in the non-doped matrix and including Zn2+⋯OC coordination, emerge in parallel. "Free" and weakly coordinated CF 3SO3- ions, present in all the xerogels studied, appear to be the main charge carriers of the conductivity maximum of this family of ormolytes located at n = 60 at 30 °C. In materials with n ≤ 20 contact ion pairs, "cross-link separated" ions pairs and higher ionic aggregates appear. The data reported demonstrate that the behaviour of the di-ureasils doped with triflate salts depends on the type of cation.

Denna post skapades 2009-12-04.
CPL Pubid: 102814


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