We report, using an electron spectrometer equipped with both monochromatized Al Kα and unmonochromatized Mg Kα sources, the quantitative characterization of the surface content, hydrolysis ratio, and condensation degree of polyalkoxysiloxane segregated to the surface of a polyurethane crosslinked film consisting of acryl polyol, polyisocyanate, and polyalkoxysiloxane. Unmonochromatized Mg Kα X‐ray irradiation extremely accelerated the decomposition of alkoxy groups of polyalkoxysiloxane. The surface content and hydrolysis ratio were determined from C 1s, Si 2p, and N 1s spectral intensities measured with monochromatized Al Kα X rays after decomposition by unmonochromatized Mg Kα X‐ray irradiation. The condensation degree was determined by the kinetic energy of the silicon KLL Auger electron after decomposition. We applied the established characterization method for a polyurethane film containing polyalkoxysiloxane. After 20 days, the surface content of polyalkoxysiloxane was greater than 60 wt %, the hydrolysis ratio ranged from 0.8 to 0.95, and the higher hydrolysis ratio resulted in a larger condensation degree. The hydrophilicity of the film surface became higher as the surface content and hydrolysis ratio increased, and the crack density became higher as the condensation degree increased. A method for characterizing the practical properties of coating film surfaces containing polyalkoxysiloxane was established. © 2002 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 40: 2917–2926, 2002

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Partially substituted ethyl silicates were synthesized by the transesterification reaction of ethyl silicate with 2-substituted ethanol. The cation-exchange resin catalyst having sulfo group was favorable as a catalyst.Hydrolysis of these silicates was studied at 60°C in water. Partial substitution was enough to enhance the hydrolyzability of silicates. Alkoxy, dimethylamino, and chloro substituents were consequently found to enhance the hydrolyzability of 2-substituted ethoxy groups, as well as ethoxy groups.

Poly(methylsilsesquioxane) (PMSQ) was synthesized using a two‐step process consisting of hydrolysis of methyl trimethoxysilane (MTMS) with aluminum chelate catalyst and successive condensation reactions conducted at elevated temperatures. Results of nuclear magnetic resonance and Fourier transform infrared measurements show that all terminal functional groups were SiOH in PMSQ. Results show further that PMSQ has both a cage structure and a network structure, and a cage/network ratio is represented by a height ratio of −64.5/−66.6 ppm. PMSQ of different molecular weight but the same SiOH concentration is obtainable by varying the condensation reaction conditions such as the concentration, temperature, amount of aluminum chelate catalyst, and the solvent solubility parameter. A difference of the cage/network ratio occurs. A different cage/network ratio is dependent on the different reactivities of the intramolecular and intermolecular reactions. The relations of molecular structure of the obtained PMSQ molecular structure were characterized along with functions of storage stability, film hardness, and weather resistance. PMSQ designed with a larger cage/network ratio is necessary to obtain PMSQ with good storage stability and a coating film having good weather resistance. PMSQ designed with a smaller cage/network ratio should be prepared to obtain a coating film with high hardness. © 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2013