Optical part made from injection molding object and resin composition for forming same
A technology of injection molding and resin composition, applied in optical elements, diffusing elements, applications, etc., can solve the problems of rising cost, difficulty in injection molding, expensive ring-opening polymerization catalyst, etc., and achieve high transparency and high The effect of refractive index
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[0220] Hereinafter, the present invention will be described in more detail based on examples, but the present invention is not limited by these examples. In the following examples and comparative examples, "parts" and "%" mean "parts by weight" and "% by weight" unless otherwise specified.
[0221] [Evaluation of Cyclic Olefin-Based Resin (B)]
[0222]
[0223] Gel permeation chromatography (HLC-8220GPC manufactured by Tosoh Corporation, column: guard column H manufactured by Tosoh Corporation) XL -H, TSK gel G7000H XL 、TSK gel GMH XL Two sticks and TSKgel G2000H XL Sequential connection; solvent: tetrahydrofuran; flow rate: 1 mL / min; sample concentration: 0.7 to 0.8% by weight; injection volume: 70 μL; measurement temperature: 40°C; Standard Polystyrene), the weight average molecular weight (Mw) and molecular weight distribution (Mw / Mn) of polystyrene (A) and cyclic olefin resin (B) were measured.
[0224]
[0225] Using a TGA thermal balance (manufactured by SII Cor...
Synthetic example 1
[0231]
[0232] The 8-methyl-8-methoxycarbonyltetracyclo[4.4.0.1 shown in the following formula (2) 2,5 .1 7,10 100 g of ]-3-dodecene (DNM), 3.6 g of 1-hexene as a molecular weight modifier, and 200 g of toluene were put into a reaction vessel replaced with nitrogen, and heated to 80°C. Add 0.21 mL of triethylaluminum (0.6 mol / L) toluene solution and methanol-modified WCl 6 0.86 mL of toluene solution (0.025 mol / L) was reacted at 80° C. for 1 hour to obtain a ring-opened polymer solution. Then, RuHCl(CO)[P(C 6 h 5 ) 3 ] 3 0.04 g, make the hydrogen pressure 9-10 MPa, and react at a temperature of 160-165° C. for 3 hours. After completion of the reaction, the obtained product was precipitated in a large amount of methanol to obtain a cyclic olefin resin (B1).
[0233] The obtained cyclic olefin resin (B1), Mw=14.4×10 4 , Mw / Mn=3.25, Tg=167°C, hydrogenation rate=99.0% or more.
[0234]
Synthetic example 2
[0236]
[0237] The 8-methyl-8-methoxycarbonyltetracyclo[4.4.0.1 shown in the above formula (2) 2,5 .1 7,10 ]-3-dodecene (DNM) 585g (2.518mol), 5-methyl-5-methoxycarbonylbicyclo[2.2.1]hept-2-ene 315g (1.895mol), as molecular weight regulator 1 35.2 g (0.419 mol) of -hexene and 1,350 g of toluene were placed in a reaction vessel replaced with nitrogen, and heated to 80°C. Add 4.70mL of triethylaluminum toluene solution (concentration of triethylaluminum is 0.61mol / L) and methanol modified WCl 6 Toluene solution (methanol modified WCl 6 The concentration is 0.025mol / L) 17.65mL, and reacted at 80°C for 1 hour to obtain a ring-opened copolymer solution.
[0238] 370 g of the obtained ring-opened copolymer solution was put into a reaction kettle, and 80 g of toluene was added. Then, RuH(OCOCH 3 )(CO)[P(C 6 h 5 ) 3 ] 2 After 0.032g, introduce hydrogen gas to make the gauge pressure reach 10MPa, keep the pressure at 10MPa, heat to 160-165°C, and carry out the reaction for ...
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