Curable resin composition, cured product, surface-processed cured product, and laminate
A technology of curable resin and composition, which is applied in the fields of surface treatment cured products and laminates, curable resin compositions, and cured products. It can solve the problems of high manufacturing costs and complicated manufacturing processes, and achieve excellent adhesion, Small surface roughness and excellent electrical properties
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[0159] Hereinafter, the present invention will be specifically described with reference to Examples and Comparative Examples. In addition, unless otherwise specified, the part and % in each example are a weight standard. Various physical properties were evaluated according to the following methods.
[0160] (1) Amount of monomer in the polymerization solution: The polymerization solution was diluted with tetrahydrofuran, and measured by gas chromatography (GC) to determine the amount of monomer in the polymerization solution.
[0161] (2) Number-average molecular weight (Mn) and weight-average molecular weight (Mw) of the polymer: measured by gel permeation chromatography (GPC) using tetrahydrofuran as a developing solvent, and obtained as polystyrene-equivalent values.
[0162] (3) The hydrogenation rate of the polymer: The hydrogenation rate refers to the ratio of the number of moles of hydrogenated unsaturated bonds to the number of moles of unsaturated bonds in the polyme...
Synthetic example 1
[0172] As the first stage of polymerization, 35 parts by mole of 5-ethylene-bicyclo[2.2.1]hept-2-ene (hereinafter, abbreviated as "EdNB"), 0.9 parts by mole of 1-hexene, and 340 parts by anisole Mole parts and 4-acetoxybenzylidene (dichloro)(4,5-dibromo-1,3-bis(trimethylphenyl)-4-imidazoline-2-ylidene) as a ruthenium-based polymerization catalyst (Tricyclohexylphosphine)ruthenium (C1063, manufactured by Wako Pure Chemical Industries, Ltd.) 0.005 mole parts were charged into a pressure-resistant glass reactor replaced with nitrogen, and polymerization was carried out at 80° C. for 30 minutes while stirring to obtain norbornenes. Ring-opened polymer solution.
[0173] Next, as the second stage of polymerization, tetracyclic [9.2.1.0 2,10 .0 3,8 ]Tetradec-3,5,7,12-tetraene (methanotetrahydrofluorene, hereinafter, abbreviated as "MTF".) 35 parts by mole, bicyclo[2.2.1]hept-2 -ene-5,6-dicarboxylic acid anhydride (hereinafter referred to as "NDCA") 30 mole parts, anisole 250 mole...
Synthetic example 2
[0176] Put 70 molar parts of MTF, 30 molar parts of NDCA, 0.9 molar parts of 1-hexene, 590 molar parts of anisole and 0.015 molar parts of C1063 into a pressure-resistant glass reactor replaced by nitrogen, and carry out the reaction at 80°C for 1 hour under stirring. Polymerization reaction to obtain norbornene ring-opening polymer solution. As a result of measuring this solution by gas chromatography, it was confirmed that substantially no monomer remained, and the polymerization conversion rate was 99% or more.
[0177] Next, the obtained ring-opening polymer solution was placed in a high-pressure reactor equipped with a stirrer replaced with nitrogen, and stirred at 150° C. under a hydrogen pressure of 7 MPa for 5 hours to perform a hydrogenation reaction to obtain a hydrogenated product of a norbornene-based ring-opening polymer. That is, the alicyclic olefin polymer (A-2) solution. The obtained polymer (A-2) had a weight average molecular weight of 50,000, a number aver...
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