Patent Application
20160319103
The present invention relates to a curable composition for optical semiconductor devices. The curable composition after curing exhibits good mechanical properties, barrier properties, heat resistance and light resistance. The present invention further relates to the use of the curable composition in production of an optical semiconductor device.
For light emitting devices such as light emitting diodes (LEDs) and photo coupler, a composition for sealing the light emitting element is required to provide the element with high thermal stability and UV stability.
Optical materials in electric and optical applications have attracted considerable attention in recent years. In the electric and optical application, the materials need to have good UV resistance, thermal aging, high transmittance, and barrier properties. These requirements are very critical and need to be fulfilled by the organic materials used. Previously, mainly epoxy resin was used as the optical material; it shows good mechanical and barrier properties. But it is prone to yellowing under exposure to UV light and/or high temperatures. That is why it was substituted by silicone material. Organopolysiloxane compositions show better heat stability and light stability than those of epoxy systems. But its barrier property is poor. So materials which have good UV/thermal resistance and good barrier properties are mostly wanted for optical applications, especially for LED applications.
Many references deal with such silicone compositions and their use for LED manufacturing.
JP 2003113310 provides a composition comprising: (A) an organic compound which contains in a molecule thereof at least two carbon-carbon double bonds showing reactivity with a SiH group, (B) a silicon compound which contains at least two SiH groups in one molecule, wherein the component (B) is a reaction product from 1,3,5,7-tetramethylcyclotetrasiloxane and triallyl isocyanurate, (C) a hydrosilylation catalyst, (D) a silane coupling agent, and (E) a silanol condensation catalyst. The elongation of the cured compositions according to the examples is less than 20%. The toughness is poor and the cured compositions easily crack when used as encapsulant in an LED cup.
JP 2012052025 provides a composition comprising: (A) organic compounds having ≧2 SiH-reactive C—C double bonds, (B) linear polyorganosiloxanes having ≧2 SiH groups and a weight average molecular weight Mw from 500 to10,000 g/mol, (C) compatibilizers, (D) hydrosilylation catalysts. To overcome compatibility problems of the compounds used in this system, compatibilizers must be used. This imposes severe limitations to adjust the formulation.
JP 2006213899 provides a composition comprising: (A) organic compound which contains at least two carbon double bond in 1 molecules which possesses reactivity with a SiH group, (B) a chemical compound which at least contains two SiH groups per molecule, (C) a hydrosilylation catalyst, and (D) a solid component having a low modulus of elasticity. The formulation needs to comprise the solid component of low modulus of elasticity such as silicone rubber particles, modacrylic rubber particles, butadiene rubber particles or fluorine rubber particles. This again imposes limitations on the possibilities to adjust the formulation.
WO 2006057218 discloses compositions comprising: (A) an organic compound having ≧2 C═C bonds reactive with an SiH group, (B) a compound having ≧2 SiH groups, (C) a hydrosilylation catalyst, and (D) rubber particles coated with an acrylic resin. The formulation needs to comprise the rubber coated with an acrylic resin. This will decrease the thermal stability.
From the above documents, it can be seen that organopolysiloxane compositions are widely used as LED encapsulant material. Organopolysiloxane compositions show better heat stability and light stability but its barrier property is poor. Moreover, in compositions known in the prior art, normally specific additives, like hardener orcompatibilizers are needed to improve the performance.
Thus, materials which have good UV/thermal resistance and good barrier properties and which do not need addition of specific additives, are still needed for optical applications, especially for LED applications.
The present invention relates to a curable composition, comprising: a) at least one organic compound having two or more carbon-carbon double bonds which is represented by formula (1):
wherein R1 at each occurrence independently from each other represents a monovalent organic group having 1 to 20 carbon atoms, b) at least one silicon hydride compound comprising at least two hydrogen atoms each directly bonded to a silicon atom and at least one aryl or arylene group per molecule, and c) at least one hydrosilylation catalyst. The curable composition after curing exhibits good mechanical properties, barrier properties, heat resistance and light resistance.
The present invention further encompasses the use of the curable composition in the production of an optical semiconductor device, in particular as an encapsulant, adhesive or lens material in the production of LEDs.
In the following passages the present invention is described in more detail. Each aspect so described may be combined with any other aspect or aspects unless clearly indicated to the contrary. In particular, any feature indicated as being preferred or advantageous may be combined with any other feature or features indicated as being preferred or advantageous.
In the context of the present invention, the terms used are to be construed in accordance with the following definitions, unless a context dictates otherwise.
As used herein, the singular forms “a”, “an” and “the” include both singular and plural referents unless the context clearly dictates otherwise.
The terms “comprising”, “comprises” and “comprised of” as used herein are synonymous with “including”, “includes” or “containing”, “contains”, and are inclusive or open-ended and do not exclude additional, non-recited members, elements or method steps.
The recitation of numerical end points includes all numbers and fractions subsumed within the respective ranges, as well as the recited end points.
Unless otherwise defined, all terms used in the disclosing the invention, including technical and scientific terms, have the meaning as commonly understood by one of the ordinary skill in the art to which this invention belongs to. By means of further guidance, term definitions are included to better appreciate the teaching of the present invention.
The present invention provides a curable composition, comprising: a) at least one organic compound having two or more carbon-carbon double bonds which is represented by formula (1):
wherein R1 at each occurrence independently from each other represents a monovalent organic group having 1 to 20 carbon atoms, b) at least one silicon hydride compound comprising at least two hydrogen atoms each directly bonded to a silicon atom and at least one aryl or arylene group per molecule, and c) at least one hydrosilylation catalyst. The curable composition provides cured products showing good mechanical properties, barrier properties, heat resistance, and light resistance.
A “curable composition” is understood to be a mixture of two or more substances which mixture can be converted from a soft state into a harder state by means of physical or chemical actions. Those physical or chemical actions can consist, for example, in the delivery of energy in the form of heat, light, or other electromagnetic radiation, but also in simply bringing into contact with atmospheric moisture, water, or a reactive component. Preferably, the composition of the present invention is heat-curable.
A curable composition according to the present invention comprises an organic compound having two or more carbon-carbon double bonds which is represented by formula (1):
wherein R1 at each occurrence independently from each other represents a monovalent organic group having 1 to 20 carbon atoms.
It is apparent from formula (1) that the required carbon-carbon double bonds need to be part of the the substituents R1. It is possible that one substituent R1 comprises 2 carbon-carbon double bonds not directly linked to each other and the remaining substituents R1 do not comprise a carbon-carbon double bond. However, it is preferred that at least two substituents R1, preferably all three substituents R1, comprise at least one carbon-carbon double bond each. Preferably, the carbon-carbon double bond(s) is/are located at the terminus of the substituent(s) R1.
Hence, preferably, in formula (1) at least two R1, preferably all three substituents R1, are selected from alkenyl groups and alkoxy alkyl groups bearing a terminal vinyl group, particularly preferred from alkenyl groups. It is possible that the alkenyl groups and alkoxy alkyl groups bear one or more halogen atoms.
Preferred alkenyl groups are selected from vinyl, allyl, 3-butenyl, 5-hexenyl, and 9-decenyl, preferably from allyl, 5-hexenyl, and 9-decenyl, particular preferred allyl. Preferred alkoxy alkyl groups are selected from vinyloxymethyl, allyloxymethyl vinyloxyethyl, and allyloxyethyl, particular preferred allyloxyethyl.
Most preferably, the organic compound of formula (1) is triallyl isocyanurate being represented by the following formula:
Triallyl isocyanurate (C12H15N3O3; mol. wt.=249.30), also called 1,3,5-triallylisocyanuric acid; or TAIC, is a commercially available compound, usually used as a crosslinking agent in the manufacture of synthetic rubbers, flame retardants, and agrochemicals. The brominated form is marketed as a flame retardant for olefin and styrene resins, providing heat and weather resistance, good dispersability, and high heat stability (to prevent yellowing).
Triallyl isocyanurate has three C—C double bonds and is able to react with silicone material which has at least one Si—H group in a hydrosilylation reaction. Triallyl isocyanurate showsgood compatibility with silicone systems and gives good transparency when such system is cured. Triallyl isocyanurate has a triazine ring, which is stable under heat and light. So presence of this compound in a curable silicone based composition does not decrease the heat/UV stability of the hybrid material resulting therefrom upon curing.
Therefore, the inventors introduced organic compounds of formula (1) and in particular triallyl isocyanurate into the field of silicone chemicals. Compared to pure silicone material, it is found that triallyl isocyanurate improves the mechanical properties and barrier properties a lot, and thereby overcomes the shortcomings of silicone material. Due to these good properties, this kind of hybrid material is beneficial for the application in production of optical semiconductor devices.
Triallyl isocyanurate is available commercially from the following sources: Sinopharm Chemical Reagent Co.Ltd. (China); Interbusiness Group, USA, Inc. (New York, N.Y.); Monomer-Polymer & Dejac Labs, Inc. (Feasterville, Pa.); Nipa Hardwicke, Inc. (Wilmington, Del.); Itochu Specialty Chemicals, Inc. (White Plains, N.Y.); Azko-Nobel Chemicals, Inc. (Chicago, Ill.); and Aldrich Chemical Co. (Milwaukee, Wis.). It is also available from Nippon Kasai Chemical Company, Ltd. (Japan) (CW Buyer's Guide, 1998). The brominated form, known as Firecut-66 (Anon., 1986), is available from Suzuhiro Chemical (Japan).
The curable composition according to the present invention preferably comprises from 2 to 55% by weight of the organic compound of formula (1), based on the total weight of the curable composition.
The curable composition according to the present invention further comprises at least one silicon hydride compound comprising at least two hydrogen atoms each directly bonded to a silicon atom and at least one aryl or arylene group per molecule.
The silicon hydride compound is preferably represented by the average compositional formula (2):
R2aHbSiO(4-a-b)/2, (2),
wherein R2 is a monovalent organic group, selected from alkyl groups, aryl groups and arylene groups; “a” is a positive number of 0.7 to 2.1, “b” is a positive number of 0.001 to 1.0, and the sum of a+b is 0.8 to 3. At least part of R2 needs to be aryl or arylene to ensure that the silicon hydride compound comprises at least one aryl or arylene group per molecule.
It is preferred that the alkyl group is an alkyl group of 1 to 10 carbon atoms, preferably selected from methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, tert.-butyl, n-pentyl, isopentyl, 2,2-dimethylpropyl, n-hexyl, isohexyl, 2,2-dimethylbutyl, n-octyl, n-nonyl, and n-decyl, particularly preferred selected from methyl, and ethyl, most preferred methyl.
The preferred aryl group is an aryl group of 6 to 10 carbon atoms, preferably selected from phenyl and benzyl, most preferred phenyl.
The preferred arylene group is an arylene group of 6 to 10 carbon atoms, preferably selected from phenylene and benzylene, most preferred phenylene.
It is particularly preferred that part of R2 designates methyl, and the remaining part of R2 designates phenyl.
Particularly preferred the silicon hydride compound is selected from
1,1,5,5-tetramethyl-3,3-diphenyl-trisiloxane,
1,1,7,7-tetramethyl-3,3,5,5-tetraphenyltetrasiloxane;
Hydride terminated polyphenyl-(d imethylsiloxy)siloxane;
Hydride terminated polyphenylene-(dimethylsiloxy)siloxane; and mixtures thereof.
Most preferred the silicon hydride compound is
1,1,5,5-tetramethyl-3,3-diphenyl-trisiloxane.
The curable composition according to the present invention preferably comprises from 45 to 98% by weight of the silicon hydride compound, based on the total weight of the curable composition.
The curable composition according to the present invention comprises a hydrosilylation catalyst.
The term “Hydrosilylation” describes the addition of Si—H bonds across unsaturated bonds. Ordinarily the reaction is conducted catalytically and usually the substrates are unsaturated organic compounds. Alkenes and alkynes give alkyl and vinyl silanes; aldehydes and ketones give silyl ethers.
Suitable hydrosilylation catalysts to be used in the present invention are platinum catalysts, for example chloroplatinic acid, allylsiloxane-platinum complex catalyst, supported platinum catalysts, methylvinylsiloxane-platinum complex catalysts, reaction products of dicarbonyldichloroplatinurn and 2,4,6-triethyl-2,4,6-trimethylcyclotrisiloxane.
Preferably, the hydrosilylation catalyst is selected from allylsiloxane-platinum complex catalyst, methylvinylsiloxane-platinum complex catalysts.
Preferably, the curable composition comprises a platinum based hydrosilylation catalyst in an amount that the platinum content calculated as platinum metal is 1 to 500 ppm, and more preferably 2 to 100 ppm, based on the total weight of the curable composition as used therein, “ppm” is to be understood as parts per million by weight.
Preferably, the curable composition according to the present invention comprises from 0.0001 to 0.05% by weight of the hydrosilylation catalyst, based on the total weight of the curable composition.
Preferably, the curable composition comprises:
However, the curable composition according to the invention may comprise further compounds and additives insofar as the objects of the invention are not compromised.
Possible additives include addition reaction inhibitors for adjusting curing time and imparting a pot life, and adhesion promoters to improve the adhesive properties of the composition. Further additives include plasticizers, stabilizers, antioxidants, reactive diluents, drying agents, UV stabilizers, anti-ageing agents, rheological auxiliaries, fungicides and/or flame retardants.
Suitable reaction inhibitors include ethynylcyclohexanol, 2-methyl-3-butyn-2-ol, 3,5-dimethyl-1-hexyn-3-ol, 2-phenyl-3-butyn-2-ol, or similar alkyne alcohols; 3-methyl-3-penten-1-yne, 3,5-dimethyl-3-hexen-1-yne, or a similar enyne compound; 1,3,5,7-tetramethyl-1,3,5,7-tetravinyl-cyclotetrasiloxane, 1,3,5,7-tetramethyl-1,3,5,7-tetrahexenyl-cyclotetrasiloxane, benzotriazole, or the like. There are no special restrictions with regard to the quantities in which these inhibitors can be added but it may be recommended that in terms of weight units these inhibitors be added in a quantity of 10 to 1,000 ppm per weight of the composition.
An adhesion promoter is understood to mean a substance that improves the adhesion properties of the composition on surfaces. Conventional adhesion promoters (tackifiers) known to the person skilled in the art can be used individually or as a combination of several compounds. Suitable examples include resins, terpene oligomers, coumarone/indene resins, aliphatic petrochemical resins and modified phenolic resins. Suitable within the framework of the present invention are, for example, hydrocarbon resins, as obtained by polymerization of terpenes, mainly α- or β-pinene, dipentene or limonene. Polymerization of these monomers is usually cationic with initiation using Friedel-Crafts catalysts. The terpene resins also include copolymers of terpenes and other monomers, such as styrene, a-methylstyrene, isoprene and the like. The above-mentioned resins are used, for example, as adhesion promoters for pressure-sensitive adhesives and coating materials. Also suitable are the terpene phenolic resins, which are produced by acid-catalyzed addition of phenols to terpenes or rosin. Terpene phenolic resins are soluble in most organic solvents and oils and miscible with other resins, waxes and rubber. Also suitable as adhesion promoters within the framework of the present invention in the above sense are the rosins and their derivatives, such as esters or alcohols thereof. Particularly suitable are silane adhesion promoters, in particular aminosilanes and epoxysilanes, for example 3,4-epoxycyclohexylethyl trimethoxysilane.
Furthermore, the curable composition according to the present invention may optionally comprise an organopolysiloxane represented by formula (3):
(R3R4R5SiO1/2)m·(R6R7SiO2/2)D·(R8SiO3/2)T·(SiO4/2)Q (3),
wherein R3 to R8 are identical or different groups independently from each other selected from alkyl groups, alkenyl groups and aryl groups, at least one of R3to R8 is an alkenyl group, at least one of R3to R8 is an aryl group, and on average at least two alkenyl groups and at least one aryl group are contained in each organopolysiloxane molecule; M, D and Q each represent a number ranging from 0 to less than 1, 0<T<1 and M+D+T+Q =1.
Preferably, R3to R8 each independently are linear or branched C1-C20 alkyl or C2-C20 alkenyl groups, or halides of such linear or branched alkyl or alkenyl groups, or cycloalkyl groups or cycloalkenyl groups having 5-25 carbon atoms, respectively, or halides of such cycloalkyl groups or cycloalkenyl groups.
It is further preferred that the alkyl group is an alkyl group of 1 to 10 carbon atoms, preferably selected from methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, tert.-butyl, n-pentyl, isopentyl, 2,2-dimethylpropyl, n-hexyl, isohexyl, 2,2-dimethylbutyl, n-octyl, n-nonyl, and n-decyl, particularly preferred selected from methyl, and ethyl, most preferred methyl.
Preferred alkenyl groups are selected from alkenyl groups of 2 to 10 carbon atoms, preferably selected from vinyl, allyl, but-1-enyl, but-2-enyl, and but-3-enyl, particularly preferred from vinyl and allyl.
The preferred aryl group is an aryl group of 6 to 10 carbon atoms, preferably selected from phenyl and benzyl, most preferred phenyl.
Preferably, the curable composition according to the present invention further comprises filler.
Suitable filler is preferably selected from the group consisting of silica, alumina, magnesium oxide, aluminum hydroxide, titanium dioxide, potassium titanate, zirconium oxide, zinc sulfide, zinc oxide and magnesium oxide.
Hence, in one preferred embodiment of the present invention the curable composition comprises:
Again, it is possible to add further additives, in particular the additives mentioned above.
Hence, in one preferred embodiment of the present invention the curable composition comprises:
A further aspect of the present invention is the use of the curable composition in production of an optical semiconductor device, in particular a LED. Preferably, the curable composition is used as encapsulant, adhesive or lens forming material in the production of LEDs.
As follows is a description of particular aspects of the present invention using a series of examples, however, the present invention is in no way restricted to the below presented examples.
Test Methods:
Hardness was measured with a LX-A and TH210 Shore durometer
Transmittance was measured by an UV-Visible spectrum analyzer Lambda 650S manufactured by PerkinElmer Corporation. The transmittance was measured for the range from 300 nm to 800 nm, and the value at 400 nm was recorded as the transmittance.
5 g triallyl isocyanurate (from Sinopharm Chemical Reagent Co. Ltd.), 15 g 1,1,5,5-tetramethyl-3,3-diphenyl-trisiloxane (from Gelest), 0.01 g 3,5-dimethyl-1-hexyn-3-ol as reaction inhibitor, and platinum-divinyltetramethyldisiloxane complex as a catalyst with the platinum content being controlled to 80 ppm (by weight) are stirred, mixed and defoamed. The mixture was cured under 150° C. for 5 hours.
The hardness of the resulting silicone material after curing was shore D 40, and the transparency at 400 nm was 88%.
After 150° C., 400nm UV aging for 24 hours, transparency at 400 nm was above 80%.
1,1,7,7-tetrannethyl-3,3,5,5-tetraphenyltetrasiloxane synthesis: 100 g diphenydimethoxy silane (from Sinopharm Chemical Reagent Co.Ltd.) and 55 g tetramethyl disiloxane were added into a three-neck bottle. 20 g 0.1 M HCI was added and heated the reaction at 60° C. for 4 hours. The organic phase was separated and evaporated under vacuum to give a colorless liquid polymer. The hydrogen content is 3.7mmol/g.
2 g triallyl isocyanurate (from Sinopharm Chemical Reagent Co.Ltd.), 6.8 g 1,1,7,7-tetramethyl-3,3,5,5-tetraphenyltetrasiloxane (synthesized as described above), 0.008 g 3,5-dimethyl-1-hexyn-3-ol as reaction inhibitor, and platinum-divinyltetramethyldisiloxane complex as a catalyst with the platinum content being controlled to 150 ppm (by weight) are sufficiently stirred, mixed and defoamed. The mixture was cured under 150° C. for 16 hours.
The hardness of the resulting silicone material after curing was shore A 60, and the transparency at 400 nm was 90%.
After 150° C., 400nm UV aging for 24 hours, transparency at 400 nm was above 80%.
Hydride terminated polyphenyl-(dimethylsiloxy)siloxane synthesis: 100 g phenyltrimethoxy silane (from Sinopharm Chemical Reagent Co.Ltd.) and 20 g tetramethyl disiloxane were added into three-neck bottle. 20 g 0.1 M HCI was added and heated the reaction at 60 C for 4 hours. The organic phase was separated and evaporated under vacuum to give a colorless liquid polymer. The hydrogen content is 3.5mmol/g, 2 g triallyl isocyanurate (from Sinopharm Chemical Reagent Co.Ltd.), 7 g Polyphenyl-(dimethylsiloxy)siloxane, hydride terminated (synthesized in the lab), 0.009 g 3,5-dimethyl-1-hexyn-3-ol as reaction inhibitor, and platinum-divinyltetramethyldisiloxane complex as a catalyst with the platinum content being controlled at 200 ppm (by weight) are sufficiently stirred, mixed and defoamed. The mixture was cured under 150° C. for 2 hours.
The hardness of the resulting silicone material after curing was shore D 50, and the transparency at 400 nm was 89%.
After 150° C., 400 nm UV aging for 24 hours, transparency at 400 nm was above 80%.
Tri-hexenyl isocyanurate synthesis: 100 ml DMF, 10 g 1,3,5-triazinane-2,4,6-trione (from Sinopharm Chemical Reagent Co.Ltd.) and 52 g 6-bromohexene (from Sinopharm Chemical Reagent Co.Ltd.) were added into three-neck bottle. 10.8 g NaOH was added and the reaction system was heated to 105 C for 3 hours. Solvent was removed under reduced pressure. Toluene was added and washed with 1M HCl solution, distilled water and saturated NaCl solution. The organic phase was evaporated under vacuum. The desired product was purified by vacuum distillation, affording a colorless liquid (bp: 162-166 C/10 Pa, temperature of oil bath: 220 C).
5 g tri-hexenyl isocyanurate (synthesized in the lab), 10 g
1,1,5,5-Tetramethyl-3,3-diphenyl-trisiloxane (from Gelest), 0.01 g
3,5-dimethyl-1-hexyn-3-ol as reaction inhibitor, and platinum-divinyltetramethyldisiloxane complex as a catalyst with the platinum content being controlled at 80 ppm (by weight) are sufficiently stirred, mixed and defoamed.
The mixture was cured under 150° C. for 5 hours.
The hardness of the resulting silicone material after curing was shore A 60, and the transparency at 400 nm was 88%.
Tri-decenyl isocyanurate synthesis: 100 ml DMF, 10 g 1,3,5-triazinane-2,4,6-trione (from Sinopharm Chemical Reagent Co.Ltd.) and 70 g 10-bromo-1-decene (from Sinopharm Chemical Reagent Co.Ltd.) were added into three-neck bottle. 10.8 g NaOH was added and the reaction system was heated to 105C for 6 hours. Solvent was removed under reduced pressure. Toluene was added and washed with 1M HCl solution, distilled water and saturated NaCl solution. The organic phase was evaporated under vacuum. The desired product was purified by vacuum distillation, affording a colorless liquid (bp: 192-200 C/10 Pa, temperature of oil bath: 250° C.). 10 g tri-decenyl isocyanurate (synthesized in the lab), 10 g 1,1,5,5-Tetramethyl-3,3-diphenyl-trisiloxane (from Gelest), 0.01 g 3,5-dimethyl-1-hexyn-3-ol as reaction inhibitor, and platinum-divinyltetramethyldisiloxane complex as a catalyst with the platinum content being controlled at 180 ppm (by weight) are sufficiently stirred, mixed and defoamed. The mixture was cured under 150° C. for 5 hours.
The hardness of the resulting silicone material after curing was shore A 50, and the transparency at 400 nm was 88%.
1,3,5-Tris(allyloxyethyl)isocyanurate synthesis: 100 ml DMF, 30 g 1,3,5-Tris(2-hydroxyethyl) isocyanurate (from Sinopharm Chemical Reagent Co.Ltd.) and 55 g allylbromide (from Sinopharm Chemical Reagent Co.Ltd.) were added into three-neck bottle. 16 g NaOH was added and the reaction system was heated to 100C for 3 hours. Solvent was removed under reduced pressure. Toluene was added and washed with 1M HCl solution, distilled water and saturated NaCl solution. The organic phase was evaporated under vacuum. The desired product was purified by vacuum distillation, affording a colorless liquid (bp: 172-178° C./15 Pa, temperature of oil bath: 220° C.).
7 g 1,3,5-Tris(allyloxyethyl)isocyanurate (synthesized in the lab), 10 g 1,1,5,5-Tetramethyl-3,3-diphenyl-trisiloxane (from Gelest), 0.01 g 3,5-dimethyl-1-hexyn-3-ol as reaction inhibitor, and platinum-divinyltetramethyldisiloxane complex as a catalyst with the platinum content being controlled at 200 ppm (by weight) are sufficiently stirred, mixed and defoamed. The mixture was cured under 150° C. for 5 hours.
The hardness of the resulting silicone material after curing was shore A 50, and the transparency at 400 nm was 88%.
Hydride terminated polyphenylene-(dimethylsiloxy)siloxane synthesis: 0.0024g platinum catalyst SIP 6832.2, 10 g Divinyltetramethyldisiloxane and 23 g bis[(p-Dimethylsilyi)phenyl]ether (from Gelest) were added into a 100 mL dry and clean round bottom flask (three neck). A magnetic stirrer was added and the flask was capped with a stopper and a condenser. The reaction was kept at 75° C. for 1 hour. And then the reaction was heated to 100° C. for 3 hours. A clear liquid resin was obtained. The hydrogen content of this resin is 1.6 mmol/g.
1 g triallyl isocyanurate (from Sinopharm Chemical Reagent Co.Ltd.), 7.5 g Hydride terminated polyphenylene-(dimethylsiloxy)siloxane (synthesized in the lab), 0.008 g 3,5-dimethyl-1-hexyn-3-ol as reaction inhibitor, and platinum-divinyltetramethyldisiloxane complex as a catalyst with the platinum content being controlled at 100 ppm (by weight) are sufficiently stirred, mixed and defoamed. The mixture was cured under 150° C. for 10 hours.
The hardness of the resulting silicone material after curing was shore D 40, and the transparency at 400 nm was 89%.
After 150C, 400 nm UV aging for 24 hours, transparency at 400 nm was above 80%.
2 g triallyl isocyanurate (from Sinopharm Chemical Reagent Co.Ltd.), 8 g 1,1,5,5-tetramethyl-3,3-diphenyl-trisiloxane (from Gelest), 5 g phenylvinyl silicone resin (vinyl content is 3.5mmol/g, from Runhe Chemical) 0.01 g 3,5-dimethyl-1-hexyn-3-ol as reaction inhibitor, and platinum-divinyltetramethyldisiloxane complex as a catalyst with the platinum content being controlled at 150 ppm (by weight) are sufficiently stirred, mixed and defoamed. The mixture was cured under 150° C. for 5 hours.
The hardness of the resulting silicone material after curing was shore D 40, and the transparency at 400 nm was 88%.
After 150° C., 400nm UV aging for 24 hours, transparency at 400 nm was above 80%.
5 g triallyl isocyanurate (from Sinopharm Chemical Reagent Co.Ltd.), 20 g hydride terminated polydimethylsiloxane (hydrogen content is 4mmol/g, from Sinopharm Chemical Reagent Co.Ltd), 0.01 g 3,5-dimethyl-1-hexyn-3-ol as reaction inhibitor, and platinum-divinyltetramethyldisiloxane complex as a catalyst with the platinum content being controlled at 100 ppm (by weight) are sufficiently stirred, mixed and defoamed.
The mixture was hazy and it was not possible to obtain a transparent sample.
| Number | Date | Country | |
|---|---|---|---|
| Parent | PCT/CN2014/070806 | Jan 2014 | US |
| Child | 15209853 | US |
