Curing resin composition and uses thereof
A technology of curable resin and composition, applied in nonlinear optics, instruments, coatings, etc., can solve the problems of unsatisfactory adhesion and coating properties of protective films, and achieve good adhesion and coating properties
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preparation example A-1-1
[0144] In a three-necked flask with a volume of 500 milliliters, add 0.30 mole of methyltrimethoxysilane (hereinafter referred to as MTMS), 0.45 mole of phenyltrimethoxysilane (hereinafter referred to as PTMS), 0.05 mole of 3-( Triethoxysilyl) propyl succinic anhydride (hereinafter referred to as GF-20), 0.2 moles of 3-(trimethoxysilyl) propyl methacrylate (hereinafter referred to as KBM-503) and 180 grams 4-hydroxy-4-methyl-2-pentanone (hereinafter abbreviated as DAA), and an aqueous oxalic acid solution (0.4 g of oxalic acid dissolved in 75 g of water) was added within 30 minutes while stirring at room temperature. Next, the flask was immersed in a 30° C. oil bath, and after stirring for 30 minutes, the above-mentioned reaction solution was heated to 110° C., and the stirring was continued to perform polycondensation reaction. After reacting for 6 hours, the solvent in the solution was removed by distillation to obtain polysiloxane polymer (A-1-1).
preparation example A-1-2 to A-2-2
[0146] Preparations A-1-2 to A-2-2 use the same preparation method as that of the polysiloxane polymer (A) of Preparation A-1-1, except that Preparation A-1 -2 to A-2-2 are to change the type and amount of raw materials in the polysiloxane polymer and the polymerization conditions. The formula and polymerization conditions are shown in Table 1, and will not be repeated here.
[0147]
[0148]
[0149]
Embodiment 1
[0152] Using 100 parts by weight of the polysiloxane polymer (A-1-1) obtained in the aforementioned Preparation Example A-1-1, 2,4-di-p-tolyl-6-(2-hydroxyl-4-methoxy phenyl)-1,3,5-triazine (hereinafter referred to as B-1-1) 0.1 parts by weight, 2,4-diphenyl-6-(2-hydroxy-4-methoxyphenyl)- 1,3,5-triazine (hereinafter referred to as B-2-1) 0.2 parts by weight, BYK-331 (hereinafter referred to as D-1) 0.01 parts by weight, vinyltrimethoxysilane (hereinafter referred to as E-1) 0.5 parts by weight After adding 100 parts by weight of the solvent 4-hydroxy-4-methyl-2-pentanone (hereinafter referred to as C-1), stir with a vibrating stirrer, dissolve and mix, and the curable resin composition can be obtained . The properties of this curable resin composition were measured according to the evaluation methods described later, and the results are shown in Table 2.
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