Liquid crystal display element composition, liquid crystal alignment layer, liquid crystal display element and manufacturing method thereof
A technology for a liquid crystal display element and a manufacturing method, applied in the directions of liquid crystal materials, chemical instruments and methods, instruments, etc., can solve the problems of increasing the voltage holding ratio, and achieve the suppression of the voltage holding ratio. high speed effect
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[0171] Hereafter, although an Example demonstrates this invention more concretely, this invention is not limited to these Examples.
[0172] The weight average molecular weight of each polymer in each synthesis example, the epoxy equivalent, the solution viscosity of each polymer solution, and the imidation rate of polyimide were measured by the following method.
[0173] [Weight average molecular weight of polymer]
[0174] The weight-average molecular weight Mw of the polymer is a polystyrene-equivalent value measured by gel permeation chromatography under the following conditions.
[0175] Column: Tosoh (Tosoh) Co., Ltd., TSKgelGRCXLII
[0176] Solvent: THF
[0177] Temperature: 40°C
[0178] Pressure: 68kgf / cm 2
[0179] [epoxy equivalent]
[0180] The epoxy equivalent is a value measured in accordance with the "hydrochloric acid-methyl ethyl ketone method" of JIS C2105.
[0181] [Solution Viscosity of Polymer Solution]
[0182] The solution viscosity [mPa·s] of th...
Synthetic example P1
[0188] [Synthesis Example P1: Synthesis of Polyamic Acid (P-1)]
[0189] 11.3 g (0.05 mol) of 2,3,5-tricarboxycyclopentylacetic dianhydride as tetracarboxylic dianhydride, and bicyclo[3.3.0]octane-2,4,6,8-tetracarboxylic acid -2:4,6:8-dianhydride 12.6g (0.05mol), and as diamine cholestalkoxy-2,4-diaminobenzene 5.02g (0.01mol), N-(2,4- Diaminophenyl)-4-(4-heptylcyclohexyl)benzamide 4.13g (0.01 mol), 3,5-diaminobenzoic acid 6.17g (0.04 mol), 1-(4-aminophenyl) -2,3-one hydrogen-1,3,3-trimethyl-1H-inden-6-amine 8.1g (0.03 mol) and 4,4'-dithiodiphenylamine 2.52g (0.01 mol) were dissolved in In 200 g of N-methyl-2-pyrrolidone (NMP), the reaction was carried out at 60° C. for 6 hours. Then, the reaction mixture was poured into very excess methanol to precipitate the reaction product. The polyamic acid (P-1) which is a compound (A) was obtained by washing|cleaning the collect|recovered deposit with methanol, and drying at 40 degreeC for 15 hours under reduced pressure. When the ob...
Synthetic example P2
[0190] [Synthesis Example P2: Synthesis of Polyimide (P-2)]
[0191] Polyamic acid (P-1) was obtained by carrying out the operation similar to synthesis example P1. After adjusting the obtained polyamic acid (P-1) so that it might become 10 wt% by NMP, 12.03 g of pyridine and 15.53 g of acetic anhydride were added, and dehydration ring-closure reaction was performed at 100 degreeC for 8 hours. Then, the reaction mixture was poured into very excess methanol to precipitate the reaction product. After washing the recovered precipitate with methanol, it was dried under reduced pressure at 40° C. for 15 hours to obtain a polyimide (P -2). When the obtained polyamic acid (P-2) was adjusted so that it might become 10 wt% by NMP, and the viscosity of this solution was measured, it was 530 mPa*s.
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