The reaction of poly(hydromethylsiloxane-co-methylphenylsiloxane) with zirconium (IV) n-propoxide in dry toluene leads to extensive scission of the siloxane chain and conversion of Si-H groups. These processes produce oligomeric siloxanes and organosilanes containing moisture sensitive propoxy and siloxy-zirconate groups. The obtained post-reaction solution of zirconium containing heterosiloxane oligomers is stable under anhydrous conditions for several weeks. However, its exposure to moisture initiates the hydrolytic condensation of the reactive groups leading to cross-linking and the formation of a siloxane-zirconium composite. Spin coating of the siloxane-zirconium prepolymer followed by exposure to moisture produces thin films with excellent light transparency and increased refractive index. The final coatings are characterized by ellipsometry, UV-Vis, IR, and Si MAS NMR spectroscopies.
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http://dx.doi.org/10.1002/marc.202000601 | DOI Listing |
Gels
November 2022
Faculty of Materials Science and Ceramics, AGH University of Science and Technology, Al. Mickiewicza 30, 30-059 Kraków, Poland.
Materials of the ZrO-SiO system were obtained by the sol-gel method applying two different types of ZrO precursors: zirconium (IV) n-propoxide Zr(OCH) and zirconium (IV) acetate Zr(OOCH) (organic acetic acid salt) while commonly used tetraethoxysilane TEOS was selected as SiO introducing one. ZrO concentration in synthesized samples varied from 20% to 50% (mol.).
View Article and Find Full Text PDFMacromol Rapid Commun
March 2021
Dr. S. Rubinsztajn, Prof. J. Chojnowski, Dr. U. Mizerska, Dr. M. Basko, Dr. P. Uznanski, Dr. A. Walkiewicz-Pietrzykowska, Prof. M. Cypryk, Centre of Molecular and Macromolecular StudiesPolish Academy of Sciences, Sienkiewicza 112, Lodz, 90-363, Poland.
The reaction of poly(hydromethylsiloxane-co-methylphenylsiloxane) with zirconium (IV) n-propoxide in dry toluene leads to extensive scission of the siloxane chain and conversion of Si-H groups. These processes produce oligomeric siloxanes and organosilanes containing moisture sensitive propoxy and siloxy-zirconate groups. The obtained post-reaction solution of zirconium containing heterosiloxane oligomers is stable under anhydrous conditions for several weeks.
View Article and Find Full Text PDFDalton Trans
April 2018
Nano-Structured Materials Division, CSIR-Central Glass and Ceramic Research Institute, 196, Raja S. C. Mullick Road, Kolkata 700032, India.
We observed that the hydrolysis-condensation reaction of precursors makes a significant difference in constructing ordered mesopores in electrospun ZrO2 nanofibers. Transmission-SAXS studies confirm the generation of uniform clusters of size ∼1.44 nm in the ZrOCl2·8H2O (inorganic salt) derived sol due to its relatively slow hydrolysis-condensation process.
View Article and Find Full Text PDFActa Bioeng Biomech
January 2017
Institute of Non-Ferrous Metals, Division of Powders and Composite Materials, Gliwice, Poland.
Purpose: The main objective of this study was to obtain single-phase β-ZrO2 powders with so-called soft agglomerates reproducibile morphology with acetyl-acetone as a chelating-agent. To the best of our knowledge there is no avaiable data which determine the effect of acetyl acetone on the phase composition and morphology of ceria-doped ZrO2 powders for biomedical applications.
Methods: Twenty variants of powders with different water to zirconia precursor and acetylacetone to zirconia precursor molar ratios were prepared.
J Nanosci Nanotechnol
September 2015
ZrB2 and ZrB2-SiC powders are synthesized by a sol-gel method from zirconium n-propoxide, tetraethyl orthosilicate (only for ZrB2-SiC), boric acid, and sucrose. After reduction at 1550 degrees C, both ZrB2 and ZrB2-SiC are unconsolidated, soft gray powders. The ZrB2-SiC particles have an equiaxed shape with a diameter of about 800 nm and a uniform size distribution.
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