Liquid crystal aligning agent, liquid crystal alignment layer manufacturing method and liquid crystal display device
A technology of liquid crystal alignment agent and polyamic acid, which is applied in liquid crystal materials, chemical instruments and methods, optics, etc., can solve problems such as burn-in, poor display, and lower product yield, and achieve excellent coating or printing properties , Excellent long-term reliability, and improved burn-in characteristics
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preparation example Construction
[0274] The preferred solvent used in the preparation of the liquid crystal aligning agent of the present invention contains one of the above-mentioned organic solvents, or a combination of two or more of the above-mentioned organic solvents. In the following preferred solid content concentrations, the liquid crystal aligning agent contains Each component does not precipitate, and the surface tension of a liquid crystal aligning agent exists in the range of 25-45mN / m.
[0275]The solid content concentration of the liquid crystal aligning agent of the present invention, that is, the ratio of the weight of all components other than the solvent in the liquid crystal aligning agent to the total weight of the liquid crystal aligning agent can be selected in consideration of viscosity, volatility, etc., and is preferably in the range of 1 to 10% by weight Inside. The liquid crystal aligning agent of the present invention forms a coating film as a liquid crystal aligning film by coati...
Embodiment
[0301] Hereinafter, the present invention will be described more specifically by way of examples, but the present invention is not limited thereto.
[0302] The weight-average molecular weight Mw in the following examples is a polystyrene-equivalent value measured by gel permeation chromatography (GPC) under the following conditions.
[0303] Column: manufactured by Tosoh Corporation, TSKgelGRCXLII
[0304] Solvent: THF
[0305] Temperature: 40°C
[0306] Pressure: 68kgf / cm 2
[0307] The epoxy equivalent is measured according to the "hydrochloric acid-methyl ethyl ketone method" of JIS C2105.
[0308] The solution viscosity of the polymer is measured at 25°C using an E-type viscometer for a polymer solution (solvent: N-methyl-2-pyrrolidone) with a polymer concentration of 20% by weight indicated in each synthesis example. value.
[0309] The imidization rate of polyimide is to add the polyimide solution obtained by each synthesis example into pure water, and the resulti...
Synthetic example E-1
[0316] Add 100.0 g of 2-(3,4-epoxycyclohexyl) ethyltrimethoxysilane, 500 g of methyl isobutyl ketone and 10.0 g triethylamine, mix at room temperature. Then, 100 g of deionized water was dropped from the dropping funnel over 30 minutes, followed by mixing under reflux and reacting at 80° C. for 6 hours. After the reaction, the organic layer was taken out and washed with 0.2% by weight of ammonium nitrate aqueous solution until the water after washing was neutral, then the solvent and water were distilled off under reduced pressure to obtain a viscous transparent liquid Polyorganosiloxane (EPS-1) with epoxy groups.
[0317] The polyorganosiloxane (EPS-1) was carried out 1 In H-NMR analysis, a peak derived from epoxy groups with theoretical intensity was obtained around chemical shift (δ) = 3.2 ppm, and it was confirmed that no side reaction of epoxy groups occurred during the reaction.
[0318]The polyorganosiloxane (EPS-1) had a weight average molecular weight Mw of 2,200 a...
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