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Christine J. T. Landry

Researcher at Eastman Kodak Company

Publications -  39
Citations -  1395

Christine J. T. Landry is an academic researcher from Eastman Kodak Company. The author has contributed to research in topics: Polymer & Miscibility. The author has an hindex of 17, co-authored 39 publications receiving 1369 citations. Previous affiliations of Christine J. T. Landry include Eastman Chemical Company.

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In situ polymerization of tetraethoxysilane in polymers: chemical nature of the interactions

TL;DR: In this article, the formation of molecular composites by the in situ polymerization of tetraethoxysilane in various organic polymers has been studied, and the results show that highly homogeneous, transparent composites can be formed for polymers such as poly(methyl methacrylate), poly(vinyl acetate), poly (vinyl pyrrolidone), and poly (N,N-dimethylacrylamide).
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In situ polymerization of tetraethoxysilane in poly(methyl methacrylate): morphology and dynamic mechanical properties

TL;DR: In this article, the properties of composites resulting from the formation of a cross-linked inorganic network via the polymerization of tetraethoxysilane (TEOS) in situ in a poly(methyl methacrylate) (PMMA) binder were investigated.
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Poly(vinyl acetate)/silica-filled materials: material properties of in situ vs fumed silica particles

TL;DR: In this paper, the physical properties of polyvinylacetate (PVAc) and silica were compared with those of PVAc/fumed silica (of 7-nm nominal perticle size) composites prepered by both melt-milling and solution-casting from THF or CCl 4.
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Dynamic studies of the molecular relaxations and interactions in microcomposites prepared by in-situ polymerization of silicon alkoxides

TL;DR: In this paper, in-situ polymerization of silicon alkoxide was used to prepare composites of silicon dioxide and poly(vinyl acetate) (PVAc), and FTIR, dielectric, and dynamic mechanical spectroscopy results showed that β decreased with increasing sol-gel concentration, indicating that there is a broadening in the distribution of relaxation times for PVAc chains.