• Journal of Adhesion and Interface
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• v.2 no.2
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• pp.20-27
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• 2001

Recently polycarbonate material has been utilized as windows in aircraft, buildings, and optical lens. However, while polycarbonate has excellent optical transparency, impact strength and many beneficial mechanical properties, it possesses poor abrasion resistance and weatherability. Then, there is a need for developing optically clear, anti-abrasive and weather resistant hard coating agents for polycarbonate. In this study, N-triethoxy silyl propyl quinine urethane(TESPQU) was synthesized with quinine and 3-isocyanato propyl triethoxy silane(3-IPTES). In order to introduce optically active silane in the main siloxane network, TESPQU was co-hydrolysed and co-condensed with methyl triethoxy silane(MTES) under acidic conditions. Polycarbonate sheets were coated with silica coating agents by the sol-gel method, and their abrasion resistance, ability of UV absorption and weatherability were evaluated. Coating agents containing hydroxybenzophenone as a UV absorber were also prepared to compare weatherability with TESPQU containing coating agent. TESPQU containing coating agent had good weatherability in accelerated QUV test.

• Elastomers and Composites
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• v.38 no.3
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• pp.227-234
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• 2003

Silicone composites for high voltage insulator (HVI SC) were prepared by adding aluminum trihydrate(ATH) treated by surface treatment agent to base silicone compound at the ratio oi 100:20, 100:40, 100:60, 100:80, and 100:100, respectively And also, ATH was treated by various surface treatment agents, such as stearic arid, acryl silane, and vinyl silane under compounding process. Mechanical properties and electrical properties were investigated for the various contents of ATH and surface-treatment agents. Mechanical properties such as tensile strength, elongation, and tear strength decreased as the load of ATH increased. Volume resistivity, AC break down strength, and tracking resistance for HVI SC containing ATH treated by vinyl silane were better than those for HVI SC containing ATH treated by other surface treatment agents, such as stearic acid and acryl silane. Polymer-filler interaction of silicone composites according to surface treatment agents was studied by measuring bound rubber contend(BR). From the experimental results, BR of silicone composite containing ATH treated with vinyl silane was higher than that of the others. The degree of rule for silicone composite was investigated using Rheometer. Maximum torque of silicone composites contaning ATH treated with vinyl silane was higher than that of silicone composite contaning ATH treated with other surface agents.

• Macromolecular Research
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• v.11 no.3
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• pp.202-205
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• 2003

The reactive precursors, vinyl ethers, and epoxy-silicones, were synthesized. The vinyl ether monomers were prepared from primary alcohol and ethyl vinyl ether with mercury (II) acetate. The epoxy-functionalized silicones have been achieved by the controlled, rhodium-catalyzed, chemoselective hydrosilation of vinyl ether with siloxanes or silane. It was shown that the hydrosilation proceeds exclusively at the vinyl ether group of alkenyl vinyl ether without participation at the alkenyl group. The photoinduced cationic polymerization of these monomers was studied and found to be all highly reactive.

• Polymer(Korea)
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• v.24 no.4
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• pp.459-468
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• 2000

To improve the mechanical properties of fiber-reinforced polymer matrix composites, laminated composites plates were fabricated using different matrix resins and glass or aramid fibers. The effect of matrix resin system were evaluated by tensile, flexural strength measurements. In the case of surface treated aramid fiber and unsaturated polyester resin composite, maximum flexural properties were observed in the composite prepared from the glass fiber treated with 0.5 wt% silane coupling agents. Vinylester resin composites show the highest tensile properties and isophthalic polyester composites have the highest flexural properties among the unsaturated polyester resin composites studied. The relationship between overlap laminated composites plates and mechanical properties of polymer composites is also investigated in order to improve mechanical properties of glass fiber and unsaturated polyester resin composites.

• Journal of Environmental Science International
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• v.26 no.1
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• pp.79-85
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• 2017

Multi-Walled Carbon Nanotubes (MWCNTs) were modified with epoxy and aminosilane diethanolamine (DEA), and nanocomposites of poly(butylene adipate-co-terephthalate) (PBAT) and the modified MWCNTs were prepared with the aim of improving the physical properties of biodegradable PBAT. The physical and the thermal properties of the PBAT/MWCNT nanocomposites were investigated using various techniques. Fourier transform infrared spectroscopy measurements revealed that the MWCNTs were efficiently modified with DEA. Scanning electron micrographs of the nanocomposites indicated that the modified MWCNTs were dispersed homogeneously in PBAT. The thermal stability of the nanocomposite decreased with increase in the content of epoxy-MWCNT-DEA due to the poor thermal stabilities of epoxy and amino silane DEA. However, the surface hydrophobicity of the nanocomposite increased. The highest stress (170% of PBAT) was observed when the content of epoxy-MWCNT-DEA in the nanocomposite was 2 wt%.

• Tribology and Lubricants
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• v.22 no.4
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• pp.182-189
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• 2006

In this paper, the adhesion characteristics between a fused silica without or with an anti-sticking layer and a thermoplastic polymer film used in thermal NIL were investigated experimentally in order to identify the release performance of the anti-sticking layer. The anti-sticking layers were derived from fluoroalkylsilanes, (1H, 1 H, 2H, 2H-perfluorooctyl)trichlorosilane ($F_{13}-OTS$) and (3, 3, 3-trifluoropropyl)trichlorosilane (FPTS), and coated on the silica surface in vapor phase. The commercial polymers, mr-I 7020 and 8020 (micro resist technology, GmbH), for thermal NIL were spin-coated on Si substrate with a rectangular island which was fabricated by conventional microfabrication process to achieve small contact area and easy alignment of flat contact sur- faces. Experimental conditions were similar to the process conditions of thermal NIL. When the polymer film on the island was separated from the silica surface after imprint process, the adhesion force between the silica surface and the polymer film was measured and the surfaces of the silica and the polymer film after the separation were observed. As a result, the anti-sticking layers remarkably reduced the adhesion force and the surface damage of polymer film and the chain length of silane affects the adhesion characteristics. The anti-sticking layers derived from FPTS and $F_{13}-OTS$ reduced the adhesion force per unit area to 38% and 16% of the silica sur-faces without an anti-sticking layer, respectively. The anti-sticking layer derived from $F_{13}-OTS$ was more effective to reduce the adhesion, while both of the anti-sticking layers prevented the surface damages of the polymer film. Finally, it is also found that the adhesion characteristics of mr-I 7020 and mr-I 8020 polymer films were similar with each other.

• Polymer(Korea)
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• v.38 no.1
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• pp.74-79
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• 2014

Microfibrillated cellulose (MFC) was chemically modified with two different silane coupling agents (3-aminopropyltriethoxysilane and 3-mercaptopropyltriethoxysilane) and lauroyl chloride. The surface modification of MFC was confirmed by infrared spectroscopy (FTIR), energy dispersive X-ray spectroscopy (EDX), and contact angle measurements. Composite paper was successfully prepared with surface modified MFC and polyamide (PA) fiber. The surface modification of MFC not only prevented aggregation of MFC but also improved adhesive property between PA fiber and surface modified MFC. It was impossible to prepare papers of only PA fiber because there is no binder to connect PA fibers. That is, surface modified MFC as a binder in PA fiber played a crucial role in making composite paper. Composite paper with silane modified MFC showed higher tensile strength and modulus than composite paper with lauroyl moiety modified MFC. The structure, morphology, and mechanical properties of composite paper were analyzed by scanning electron microscope (SEM) and universal testing machine (UTM).

• Macromolecular Research
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• v.15 no.2
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• pp.147-153
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• 2007

Hyperbranched polysiloxysilanes (HBPSs), with a variety of terminal functional groups (vinyl, epoxy, carboxyl and hydroxyl), were synthesized by the self-polymerization of an $AB_3$ type monomer of tris(dimethylvinylsiloxy) silane, with subsequent end-functionalizations, such as epoxidation and radical addition reaction, respectively. The ratio of the $\alpha-and$ $\beta-addition$ linkages in the HBPS polymerized by hydrosilylation of the $AB_3$ monomer was found to be approximately 1 to 3. The thermal stability and solubility were affected by the terminal functional groups.

• Bulletin of the Korean Chemical Society
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• v.17 no.5
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• pp.443-447
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• 1996

Several polysilanes with sterically bulky substituents such as poly(2-phenylpropyl)(n-hexyl)silane were prepared by Wurtz-type coupling. The polysilane products were mixtures of low-molecular-weight polymers (&bar{M};w~103) as major and high-molecular-weight polymers (&bar{M};w~106) as minor. Overall yields for polysilanes were in the range of 81-99%. λmax of liquid low MW polymers appeared at around 280 nm. Formations of solid high MW polymers were decreased by a longer reaction time and increased steric bulkiness of substituents. High MW polymers with λmax at 327 nm except crosslinked polymers were soluble in common organic solvents and found to be light sensitive. Crosslinked high MW polymer gave 21% TGA ceramic yield, compared with linear high polymer giving zero ceramic yield.

• Bulletin of the Korean Chemical Society
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• v.22 no.12
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• pp.1337-1340
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• 2001

The bulk photopolymerization of methyl methacrylate (MMA) with para-substituted phenylsilanes such as F-C6H4SiH3 (1), H3C-C6H4SiH3 (2), and H3CO-C6H4SiH3 (3) was performed to produce poly(MMA)s containing the respective silyl moiety as an end group. For all the hydrosilanes, the polymerization yields and the polymer molecular weights decreased, whereas the TGA residue yields and the relative intensities of Si-H IR stretching bands increased as the relative silane concentration over MMA increased. The polymerization yields and polymer molecular weights of MMA with 1-3 increased in the order of 3 < 1 < 2. These hydrosilanes influence significantly upon the photopolymerization of MMA as both chain-initiation and chain-transfer agents.