WO2016199742A1 - 付加硬化性シリコーンゴム組成物及び硬化物 - Google Patents
付加硬化性シリコーンゴム組成物及び硬化物 Download PDFInfo
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- WO2016199742A1 WO2016199742A1 PCT/JP2016/066836 JP2016066836W WO2016199742A1 WO 2016199742 A1 WO2016199742 A1 WO 2016199742A1 JP 2016066836 W JP2016066836 W JP 2016066836W WO 2016199742 A1 WO2016199742 A1 WO 2016199742A1
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- 0 *C([n]1nnc2c(*)c(*)c(*)c(*)c12)=O Chemical compound *C([n]1nnc2c(*)c(*)c(*)c(*)c12)=O 0.000 description 2
- XANMUIJUGHYRRM-UHFFFAOYSA-N CC(C)CC(C)NC([n]1nnc2ccccc12)=O Chemical compound CC(C)CC(C)NC([n]1nnc2ccccc12)=O XANMUIJUGHYRRM-UHFFFAOYSA-N 0.000 description 1
- NIIUIBKEGRPPDK-UHFFFAOYSA-N CC([n]1nnc2c1cccc2)=O Chemical compound CC([n]1nnc2c1cccc2)=O NIIUIBKEGRPPDK-UHFFFAOYSA-N 0.000 description 1
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C08K5/3467—Heterocyclic compounds having nitrogen in the ring having more than two nitrogen atoms in the ring
- C08K5/3472—Five-membered rings
- C08K5/3475—Five-membered rings condensed with carbocyclic rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/16—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms condensed with carbocyclic rings or ring systems
- C07D249/18—Benzotriazoles
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/04—Polysiloxanes
- C08G77/06—Preparatory processes
- C08G77/08—Preparatory processes characterised by the catalysts used
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/34—Silicon-containing compounds
- C08K3/36—Silica
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/54—Silicon-containing compounds
- C08K5/544—Silicon-containing compounds containing nitrogen
- C08K5/5475—Silicon-containing compounds containing nitrogen containing at least one C≡N bond
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L83/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
- C08L83/04—Polysiloxanes
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L83/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
- C08L83/14—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers in which at least two but not all the silicon atoms are connected by linkages other than oxygen atoms
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/04—Polysiloxanes
- C08G77/12—Polysiloxanes containing silicon bound to hydrogen
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/04—Polysiloxanes
- C08G77/20—Polysiloxanes containing silicon bound to unsaturated aliphatic groups
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K2201/00—Specific properties of additives
- C08K2201/002—Physical properties
- C08K2201/006—Additives being defined by their surface area
Definitions
- the present invention provides an addition curable silicone rubber composition capable of providing a cured silicone rubber exhibiting low compression set and heat discoloration without impairing the mechanical properties (rubber properties) and curing speed of the silicone rubber. Product and its cured product.
- Silicone rubber is heat-resistant, cold-resistant, safe, good in appearance (transparency), soft to the touch, and durable. It is used in a wide range of fields such as gasket materials, building materials, and fiber coating materials.
- Patent Document 1 Japanese Patent Application Laid-Open No. Hei 11 (1994)). No. 2-242854.
- a triazole-based compound is added to the silicone rubber composition, there is a problem that the curing rate decreases.
- the present invention has been made to improve the above circumstances, and by adding a benzotriazole derivative having a specific structure to the silicone rubber composition, the compression set of the cured product can be reduced without reducing the curing rate. It is an object of the present invention to provide an addition-curable silicone rubber composition and a cured product thereof.
- an addition-curable silicone rubber composition containing a silicon-bonded alkenyl group-containing organopolysiloxane, an organohydrogenpolysiloxane, and a platinum catalyst By adding a specific amount of a benzotriazole derivative having a specific structure represented by the general formula (I) to be described later to the product, a cured silicone rubber having a low compression set is obtained without impairing the curing rate. It has been found that an addition-curable silicone rubber composition that can be applied is obtained, and has led to the present invention.
- the present invention provides the following addition-curable silicone rubber composition and its cured product.
- [1] Alkenyl group-containing organopolysiloxane having an alkenyl group bonded to at least two silicon atoms in one molecule: 100 parts by mass
- (B) Organohydrogenpolysiloxane containing hydrogen atoms bonded to at least two silicon atoms in one molecule: 0.2 to 20 parts by mass with respect to 100 parts by mass of component (A),
- D The following general formula (I) (Wherein R 1 is a hydrogen atom or a monovalent hydrocarbon group having 1 to 10 carbon atoms, and R 2 is a monovalent organic group.) A benzotriazole derivative represented by the formula: 2 to 1,000 mol per 1 mol of the platinum atom of the component (C)
- an addition-curable silicone rubber composition capable of providing a silicone rubber having a low compression set without impairing the curing speed by combining specific amounts of the components (A) to (D). it can. Furthermore, the obtained silicone rubber can suppress discoloration after the heat resistance test.
- the organopolysiloxane containing an alkenyl group bonded to at least two silicon atoms in one molecule of the component (A) is a main component (base polymer) of the present composition, and as the organopolysiloxane, What is shown by the following average compositional formula (II) can be used.
- R 3 a SiO (4-a) / 2 (II) Wherein R 3 is an unsubstituted or substituted monovalent hydrocarbon group having the same or different carbon number of 1 to 15, preferably 1 to 10, more preferably 1 to 8, and a is 1.5 to 2.8, preferably 1.8 to 2.5, more preferably a positive number in the range of 1.95 to 2.05.)
- examples of the unsubstituted or substituted monovalent hydrocarbon group having 1 to 15, preferably 1 to 10, more preferably 1 to 8 carbon atoms bonded to the silicon atom represented by R 3 include methyl group, ethyl group, Group, propyl group, isopropyl group, butyl group, isobutyl group, tert-butyl group, pentyl group, neopentyl group, hexyl group, cyclohexyl group, octyl group, nonyl group, decyl group and other alkyl groups, phenyl group, tolyl group, Aryl group such as xylyl group, naphthyl group, aralkyl group such as benzyl group, phenylethyl group, phenylpropyl group, vinyl group, allyl group, propenyl group, isopropenyl group, butenyl group, hexenyl group, cyclohex
- R 3 must be alkenyl groups (preferably those having 2 to 8 carbon atoms, more preferably 2 to 6 carbon atoms, and particularly preferably vinyl groups).
- the alkenyl group content in the organopolysiloxane is 1.0 ⁇ 10 ⁇ 6 mol / g to 3.0 ⁇ 10 ⁇ 3 mol / g, particularly 1.0 ⁇ 10 ⁇ 5 mol / g to 2.0. It is preferable to set it as x10 ⁇ -3 > mol / g.
- the amount of the alkenyl group is less than 1.0 ⁇ 10 ⁇ 6 mol / g, the rubber hardness may be too low to form a gel, and if it exceeds 3.0 ⁇ 10 ⁇ 3 mol / g, the crosslinking density Becomes too high, the hardness becomes extremely high, and the elasticity of the rubber may be lost.
- the alkenyl group may be bonded to the silicon atom at the end of the molecular chain, may be bonded to the silicon atom in the middle of the molecular chain (non-terminal), or may be bonded to both.
- the structure of this organopolysiloxane basically has both molecular chain ends blocked with triorganosiloxy groups (R 3 3 SiO 1/2 ) and the main chain is a diorganosiloxane unit (R 3 2 SiO 2/2).
- the average degree of polymerization (number average degree of polymerization, hereinafter the same) is usually 100 to 50,000, preferably 150 to 20,000. If it is less than 100, the cured product may not have a sufficient rubber feeling, and if it is higher than 50,000, the viscosity becomes high and molding may be difficult.
- the molecular weight or the degree of polymerization can be determined, for example, as the number average molecular weight or number average degree of polymerization in terms of polystyrene in gel permeation chromatography (GPC) analysis using toluene as a developing solvent (hereinafter the same).
- the organopolysiloxane of component (A) molecular chain both ends diorganoalkenylsiloxy group-blocked diorganopolysiloxane, molecular chain both ends organodialkenylsiloxy group-blocked diorganopolysiloxane, molecular chain Both ends trialkenylsiloxy group-blocked diorganopolysiloxane, molecular chain both ends triorganosiloxy group-blocked diorganosiloxane / organoalkenylsiloxane copolymer, both ends chain diorganoalkenylsiloxy group-blocked diorganosiloxane / organoalkenylsiloxane
- the polymer include a diorganosiloxane / organoalkenylsiloxane copolymer in which one end of a molecular chain is blocked with a diorganoalkenylsiloxy group and the other end is a
- the “organo group” in each of the above siloxanes is the same as the unsubstituted or substituted monovalent hydrocarbon group other than the aliphatic unsaturated group such as alkenyl group among R 3 in the formula (II). Means.
- the component (B) is an organohydrogenpolysiloxane having at least 2, preferably 3 or more, hydrogen atoms bonded to silicon atoms (SiH groups) in one molecule.
- (A) It crosslinks with the alkenyl group couple
- the organohydrogenpolysiloxane of component (B) is, for example, represented by the following average composition formula (III): at least 2, preferably 3 or more, more preferably 3 to 100, Those having 4 to 50 silicon-bonded hydrogen atoms (SiH groups) are preferably used.
- R 4 is an unsubstituted or substituted monovalent hydrocarbon group having the same or different carbon number of 1 to 15, preferably 1 to 10, more preferably 1 to 8. 7 to 2.1, c is 0.001 to 1.0, and b + c is a positive number satisfying 0.8 to 3.0.
- examples of the monovalent hydrocarbon group for R 4 include the same groups as those exemplified for R 3 , but those having no aliphatic unsaturated bond are preferred.
- b is 0.7 to 2.1, preferably 0.8 to 2.0
- c is 0.001 to 1.0, preferably 0.01 to 1.0
- b + c is 0.00. It is a positive number satisfying 8 to 3.0, preferably 1.0 to 2.5.
- the molecular structure of the organohydrogenpolysiloxane is any of linear, cyclic, branched, and three-dimensional network. It may be a structure.
- the SiH group content in the organohydrogenpolysiloxane is preferably 0.0005 mol / g to 0.020 mol / g, particularly preferably 0.001 mol / g to 0.017 mol / g. If the amount of SiH groups is less than 0.0005 mol / g, crosslinking may be insufficient, and if it exceeds 0.020 mol / g, organohydrogenpolysiloxane may become an unstable substance.
- the number of silicon atoms in one molecule is preferably 2 to 300, particularly 3 to 150, particularly 4 to 100, and liquid at room temperature (25 ° C.).
- bonded with a silicon atom may be located in any of the molecular chain terminal and the middle (non-terminal) of a molecular chain, and may be located in both.
- organohydrogenpolysiloxane of component (B) examples include 1,1,3,3-tetramethyldisiloxane, 1,3,5,7-tetramethylcyclotetrasiloxane, tris (hydrogendimethylsiloxy) methylsilane, Tris (hydrogendimethylsiloxy) phenylsilane, methylhydrogencyclopolysiloxane, methylhydrogensiloxane / dimethylsiloxane cyclic copolymer, trimethylsiloxy group-blocked methylhydrogenpolysiloxane at both ends, trimethylsiloxy group-blocked dimethylsiloxane at both ends Methyl hydrogen siloxane copolymer, both ends dimethyl hydrogen siloxy group-capped dimethyl polysiloxane, both ends dimethyl hydrogen siloxy group capped dimethyl siloxane methyl high Rogen siloxane copolymer, trimethylsiloxy group-blocked methylhydrogens
- organohydrogenpolysiloxane of component (B) a part of the siloxane skeleton (—Si—O—Si—) constituting the molecule (usually oxygen that forms a siloxane bond) in the compounds exemplified above
- a part of the atom position is usually a divalent to tetravalent aromatic ring-containing hydrocarbon skeleton (eg, phenylene skeleton, bisphenylene skeleton, bis (phenylene) ether skeleton, bis (phenylene) methane skeleton, 2,
- It may be a polyaromatic ring-containing organohydrogenpolysiloxane containing a 2-bis (phenylene) propane skeleton, a 2,2-bis (phenylene) hexafluoropropane skeleton, or the like.
- the blending amount of the organohydrogenpolysiloxane as the component (B) is 0.2 to 20 parts by mass, preferably 0.3 to 10 parts by mass with respect to 100 parts by mass as the total of the component (A).
- the molar ratio (SiH group / alkenyl group) to the total amount of alkenyl groups bonded to the atoms is 0.8 to 10, particularly 1.0 to 5. If this ratio is less than 0.8, curing (crosslinking density) may be insufficient, resulting in a sticky rubber. If it is greater than 10, foaming is observed in the silicone rubber molding, or from the mold. It may be difficult to release the mold.
- platinum catalyst of component (C) platinum black, secondary platinum chloride, chloroplatinic acid, a reaction product of chloroplatinic acid and a monohydric alcohol, a complex of chloroplatinic acid and olefins, platinum bisacetoacetate, etc.
- platinum group metal catalysts platinum group metal catalysts.
- the amount of the platinum catalyst can be a catalytic amount. Normally, when the platinum group metal (in terms of mass) is used, the components (A) to (D) and the component (E) described later are combined (A ) To (E) with respect to the total mass of 0.5 to 1,000 ppm, particularly about 1 to 500 ppm.
- the component (D) has the following general formula (I): (Wherein R 1 is a hydrogen atom or a monovalent hydrocarbon group having 1 to 10 carbon atoms, preferably 1 to 6 carbon atoms, and R 2 is a monovalent organic group.)
- R 1 is a hydrogen atom or a monovalent hydrocarbon group having 1 to 10 carbon atoms, preferably 1 to 6 carbon atoms, and R 2 is a monovalent organic group.
- R 1 is a hydrogen atom or a monovalent hydrocarbon group having 1 to 10 carbon atoms, preferably 1 to 6 carbon atoms.
- the monovalent hydrocarbon group having 1 to 6 carbon atoms include a methyl group, an ethyl group, and a propyl group.
- Alkyl groups such as isopropyl group, butyl group, isobutyl group, tert-butyl group, pentyl group, neopentyl group, hexyl group, cyclohexyl group, etc., and part or all of the hydrogen atoms of these groups are fluorine, bromine, chlorine, etc.
- a halogen atom, a cyano group, etc. such as a chloromethyl group, a chloropropyl group, a bromoethyl group, a trifluoropropyl group, a cyanoethyl group, and the like.
- a hydrogen atom or a methyl group is preferable from the viewpoint of synthesis.
- R 2 is a monovalent organic group such as methyl group, ethyl group, propyl group, isopropyl group, butyl group, isobutyl group, tert-butyl group, pentyl group, neopentyl group, hexyl group, cyclohexyl group, etc.
- a monovalent hydrocarbon group having 1 to 10 carbon atoms such as an aryl group such as an alkyl group, a phenyl group, a tolyl group, a xylyl group and a naphthyl group, an aralkyl group such as a benzyl group, a phenylethyl group and a phenylpropyl group; Moreover, group etc. which are shown by a following formula are mentioned.
- R 5 is a monovalent hydrocarbon group such as an alkyl group of 1 to 15, especially 1 to 10 carbon atoms, or - (CH 2) a p -Si (OR 6) 3, R 6 is 1 to 4, especially 1-3 alkyl groups or SiR 7 3 groups (R 7 is 1-4, especially 1-3 alkyl groups), p is an integer from 1-6, especially 1-3, * is a bond Indicates a point.)
- n represents an integer of 0 to 6.
- m represents an integer of 1 to 6.
- l is an integer of 1 to 6, and R 6 is an alkyl group or a trialkylsilyl group.
- the compounding amount of the component (D) is 2 to 1,000 mol, preferably 2 to 800 mol, more preferably 2 to 500 mol, and particularly preferably 2 to 100 mol with respect to 1 mol of the platinum atom of the component (C). If the amount is less than 2 mol, the compression set cannot be lowered sufficiently, and if it exceeds 1,000 mol, the curability is lowered.
- the silicone rubber composition of the present invention preferably contains a reinforcing filler as the component (E).
- reinforcing silica fine powder is preferable as the reinforcing filler.
- the reinforcing silica fine powder of component (E) is not particularly limited in the type of silica and may be any material that is usually used as a rubber reinforcing agent.
- the reinforcing silica fine powder those used in conventional silicone rubber compositions can be used, but reinforcing silica fine powder having a specific surface area of 50 m 2 / g or more by the BET method is used.
- precipitated silica (wet silica), fumed silica (dry silica), calcined silica, etc., having a specific surface area by the BET method of 50 to 400 m 2 / g, particularly 100 to 350 m 2 / g, are preferably used to improve rubber strength.
- fumed silica is preferable.
- the reinforcing silica fine powder is, for example, a silica fine powder whose surface is hydrophobized with a surface treatment agent such as an organosilicon compound (usually hydrolyzable) such as chlorosilane, alkoxysilane, or organosilazane. There may be.
- these silica fine powders may be in a powder state and have been subjected to a surface hydrophobization treatment directly with a surface treatment agent, or may be a silicone oil (for example, an alkenyl group-containing organopolysiloxane of component (A) above).
- a surface treatment agent may be added at the time of kneading with (siloxane) to make the surface hydrophobic.
- the untreated silica fine powder and the processing agent are put in a mechanical kneading apparatus or a fluidized bed sealed at normal pressure, and an inert gas is used if necessary.
- mixing treatment is performed at room temperature or heat treatment (under heating).
- the treatment may be accelerated by using a catalyst (hydrolysis accelerator or the like).
- the treated silica fine powder can be produced by drying.
- the blending amount of the treatment agent may be equal to or more than the amount calculated from the coating area of the treatment agent.
- Specific treatment agents include silazanes such as hexamethyldisilazane, methyltrimethoxysilane, ethyltrimethoxysilane, propyltrimethoxysilane, butyltrimethoxysilane, dimethyldimethoxysilane, diethyldimethoxysilane, vinyltriethoxy.
- Silane coupling agents such as silane, vinyltrimethoxysilane, trimethylmethoxysilane, triethylmethoxysilane, vinyltris (methoxyethoxy) silane, trimethylchlorosilane, dimethyldichlorosilane, divinyldimethoxysilane and chloropropyltrimethoxysilane, polymethylsiloxane, organo Examples thereof include organosilicon compounds such as hydrogen polysiloxane, which are surface treated and used as hydrophobic silica fine powder.
- silane coupling agents or silazanes are particularly preferable.
- the blending amount of the component (E) is 1 to 100 parts by weight, preferably 5 to 60 parts by weight, more preferably 10 to 60 parts by weight with respect to 100 parts by weight of the component (A).
- the amount is less than 1 part by mass, a sufficient reinforcing effect cannot be obtained.
- the amount exceeds 100 parts by mass, the viscosity of the silicone rubber composition becomes too high, and workability and workability deteriorate.
- fillers such as quartz powder, diatomaceous earth, calcium carbonate, and conductive materials such as carbon black, conductive zinc white, metal powder, etc.
- Fillers such as quartz powder, diatomaceous earth, calcium carbonate, and conductive materials such as carbon black, conductive zinc white, metal powder, etc.
- Agents nitrogen-containing compounds, acetylene compounds, phosphorus compounds, nitrile compounds, carboxylates, tin compounds, mercury compounds, sulfur compounds and other hydrosilylation reaction control agents, iron oxides, heat-resistant agents such as cerium oxide, dimethyl silicone oil, etc.
- Internal release agent, adhesion-imparting agent in particular, the molecule contains at least one functional group selected from alkenyl group, epoxy group, amino group, (meth) acryloxy group, mercapto group, etc. It is optional to add an organosilicon compound such as alkoxysilane that does not contain a SiH group) and a thixotropic agent. That.
- a conventional method can be adopted.
- an optimal means suitable for the purpose is selected from injection molding, transfer molding, injection molding, compression molding, and the like. It is possible.
- a heat treatment (primary vulcanization) condition at 40 to 230 ° C. for about 3 seconds to 160 minutes can be employed.
- secondary vulcanization (post cure) may be optionally performed at 40 to 230 ° C. for about 10 minutes to 24 hours as necessary.
- a curing tester [rotorless type disk rheometer, moving die rheometer, or MDR] measured at 130 ° C. for 2 minutes is used.
- 10% curing time that is, time from the start of measurement when giving a torque value of 10% with respect to the maximum torque value in 2 minutes from the start of measurement at 130 ° C.
- 90% curing time that is, 130 ° C.
- T90-T10 is preferably 40 seconds or less, more preferably 40 seconds or less, where T90 (second) is the time from the start of measurement when giving a torque value of 90% with respect to the maximum torque value for 2 minutes from the start of measurement. Is 30 seconds or less. If it is longer than 40 seconds, the molding cycle is bad, which may be uneconomical.
- a cured product (silicone rubber) obtained by curing the above addition-curable silicone rubber composition is compressed by compression set measurement at a compression rate of 25%, 150 ° C., 22 hours based on JIS-K6249.
- the permanent set is 30% or less, particularly 20% or less, especially 15% or less.
- a compression set of 30% or less is preferable as an O-ring or packing material.
- the component (D) is uniformly blended at the blending ratio described above. This can be achieved.
- the addition-curable silicone rubber composition of the present invention is suitably used as a seal material for O-rings, packings, etc., especially for applications that require as low compression set as possible.
- an average degree of polymerization shows the number average degree of polymerization of polystyrene conversion in the gel permeation chromatography (GPC) analysis which used toluene as the developing solvent.
- Example 1 100 parts of dimethylpolysiloxane (A1) having an average degree of polymerization of 750 blocked at both ends of the molecular chain with dimethylvinylsiloxy groups, both ends of the molecular chain blocked with trimethylsiloxy groups as cross-linking agents, and SiH groups on the side chains
- silicone rubber compound A 0.10 parts of a toluene solution (C1) (platinum atom 1% by mass) of a complex of platinum and 1,3-divinyl-1,1,3,3-tetramethyldisiloxane was added for 15 minutes at room temperature. Stir to obtain silicone rubber compound A.
- C1 platinum atom 1% by mass
- a benzotriazole derivative (D1) represented by the following formula with respect to 100 parts of this silicone rubber compound A 0.007 part (benzotriazole derivative / Pt atom 8.5 mol / mol) was added to obtain a uniform silicone rubber composition.
- Table 1 shows the results of measuring the curability of the composition at 130 ° C. using a rheometer MDR2000 (manufactured by Alpha Technologies). Further, as a result of visually confirming the appearance (color tone) of the cured product obtained by press curing the composition at 120 ° C. for 15 minutes, compression set (compression rate 25%, temperature) was confirmed based on JIS-K6249. Table 1 shows the results of measuring 150 ° C. and the test time of 22 hours) and visually confirming the appearance (color tone) of the sample after the compression set test.
- Table 1 shows the results of measuring the curability of the composition at 130 ° C. using a rheometer MDR2000 (manufactured by Alpha Technologies). Further, as a result of visually confirming the appearance (color tone) of the cured product obtained by press curing the composition at 120 ° C. for 15 minutes, compression set (compression rate 25%, temperature) was confirmed based on JIS-K6249. Table 1 shows the results of measuring 150 ° C. and the test time of 22 hours) and visually confirming the appearance (color tone) of the sample after the compression set test.
- Table 1 shows the results of measuring the curability of the composition at 130 ° C. using a rheometer MDR2000 (manufactured by Alpha Technologies). Further, as a result of visually confirming the appearance (color tone) of the cured product obtained by press curing the composition at 120 ° C. for 15 minutes, compression set (compression rate 25%, temperature) was confirmed based on JIS-K6249. Table 1 shows the results of measuring 150 ° C. and the test time of 22 hours) and visually confirming the appearance (color tone) of the sample after the compression set test.
- Table 1 shows the results of measuring the curability of the composition at 130 ° C. using a rheometer MDR2000 (manufactured by Alpha Technologies). Further, as a result of visually confirming the appearance (color tone) of the cured product obtained by press curing the composition at 120 ° C. for 15 minutes, compression set (compression rate 25%, temperature) was confirmed based on JIS-K6249. Table 1 shows the results of measuring 150 ° C. and the test time of 22 hours) and visually confirming the appearance (color tone) of the sample after the compression set test.
- Table 1 shows the results of measuring the curability at 130 ° C. of the silicone rubber compound A of Example 1 before adding the benzotriazole derivative using a rheometer MDR2000 (manufactured by Alpha Technologies). Further, as a result of visually confirming the appearance (color tone) of the cured product obtained by press-curing the silicone rubber compound A at 120 ° C. for 15 minutes, compression set (compression rate: 25%) based on JIS-K6249. Table 1 shows the results obtained by measuring the temperature (150 ° C., test time 22 hours) and the visual appearance (color tone) of the sample after the compression set test.
- a benzotriazole derivative (D5) represented by the following formula with respect to 100 parts of the silicone rubber compound A of Example 1 0.0055 part (benzotriazole derivative / Pt atom 8.0 mol / mol) was added to obtain a uniform silicone rubber composition.
- Table 1 shows the results of measuring the curability of the composition at 130 ° C. using a rheometer MDR2000 (manufactured by Alpha Technologies). Further, as a result of visually confirming the appearance (color tone) of the cured product obtained by press curing the composition at 120 ° C. for 15 minutes, compression set (compression rate 25%, temperature) was confirmed based on JIS-K6249. Table 1 shows the results of measuring 150 ° C. and the test time of 22 hours) and visually confirming the appearance (color tone) of the sample after the compression set test.
- Example 5 60 parts of dimethylpolysiloxane (A1) having an average degree of polymerization of 750 having both ends of the molecular chain blocked with dimethylvinylsiloxy groups, and fumed silica (E1) having a specific surface area of 300 m 2 / g by BET method (Nippon Aerosil) 40 parts of Aerosil 300), 8 parts of hexamethyldisilazane, and 2.0 parts of water were mixed at room temperature for 30 minutes, heated to 150 ° C., stirred for 3 hours, cooled, and the silicone rubber base was Obtained.
- Table 2 shows the results of measuring the curability of the composition at 130 ° C. using a rheometer MDR2000 (manufactured by Alpha Technologies). Further, as a result of visually confirming the appearance (color tone) of the cured product obtained by press curing the composition at 120 ° C. for 15 minutes, compression set (compression rate: 25%, temperature) based on JIS-K6249 Table 2 shows the results of measuring 150 ° C. and 22 hours of test time) and visually confirming the appearance (color tone) of the sample after the compression set test.
- Table 2 shows the results of measuring the curability of the composition at 130 ° C. using a rheometer MDR2000 (manufactured by Alpha Technologies). Further, as a result of visually confirming the appearance (color tone) of the cured product obtained by press curing the composition at 120 ° C. for 15 minutes, compression set (compression rate 25%, temperature) was confirmed based on JIS-K6249. Table 2 shows the results of measuring 150 ° C. and 22 hours of test time) and visually confirming the appearance (color tone) of the sample after the compression set test.
- Table 2 shows the results of measuring the curability of the composition at 130 ° C. using a rheometer MDR2000 (manufactured by Alpha Technologies). Further, as a result of visually confirming the appearance (color tone) of the cured product obtained by press curing the composition at 120 ° C. for 15 minutes, compression set (compression rate 25%, temperature) was confirmed based on JIS-K6249. Table 2 shows the results of measuring 150 ° C. and 22 hours of test time) and visually confirming the appearance (color tone) of the sample after the compression set test.
- Table 2 shows the results of measuring the curability of the composition at 130 ° C. using a rheometer MDR2000 (manufactured by Alpha Technologies). Further, as a result of visually confirming the appearance (color tone) of the cured product obtained by press curing the composition at 120 ° C. for 15 minutes, compression set (compression rate 25%, temperature) was confirmed based on JIS-K6249. Table 2 shows the results of measuring 150 ° C. and 22 hours of test time) and visually confirming the appearance (color tone) of the sample after the compression set test.
- Table 2 shows the results of measuring the curability at 130 ° C. of the silicone rubber compound B of Example 5 before addition of the benzotriazole derivative using a rheometer MDR2000 (manufactured by Alpha Technologies). Further, as a result of visually confirming the appearance (color tone) of the cured product obtained by press curing the silicone rubber compound B at 120 ° C. for 15 minutes, the compression set (compression rate: 25%) was determined based on JIS-K6249. Table 2 shows the results of measuring the temperature (150 ° C., test time 22 hours) and the results of visually confirming the appearance (color tone) of the sample after the compression set test.
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Abstract
Description
〔1〕
(A)1分子中に少なくとも2個のケイ素原子に結合したアルケニル基を有するアルケニル基含有オルガノポリシロキサン:100質量部、
(B)1分子中に少なくとも2個のケイ素原子に結合した水素原子を含有するオルガノハイドロジェンポリシロキサン:(A)成分100質量部に対して0.2~20質量部、
(C)白金触媒:触媒量、
(D)下記一般式(I)
で表されるベンゾトリアゾール誘導体:(C)成分の白金原子1molに対し、2~1,000mol
を含有する付加硬化性シリコーンゴム組成物。
〔2〕
式(I)において、R2が炭素数1~10の一価炭化水素基、又は下記式
で表されるものである〔1〕記載の付加硬化性シリコーンゴム組成物。
〔3〕
(E)成分として、補強性充填剤を(A)成分100質量部に対して1~100質量部含有する〔1〕又は〔2〕記載の付加硬化性シリコーンゴム組成物。
〔4〕
(E)成分がBET法における比表面積が50m2/g以上のヒュームドシリカである〔3〕記載の付加硬化性シリコーンゴム組成物。
〔5〕
130℃における2分測定時の10%硬化時間をT10、90%硬化時間をT90としたとき、T90-T10が40秒以下となるものである〔1〕~〔4〕のいずれかに記載の付加硬化性シリコーンゴム組成物。
〔6〕
〔1〕~〔5〕のいずれかに記載のシリコーンゴム組成物を硬化してなり、圧縮率25%、150℃で22時間圧縮後の圧縮永久歪が30%以下であるシリコーンゴム硬化物。
まず、(A)成分の1分子中に少なくとも2個のケイ素原子に結合したアルケニル基を含有するオルガノポリシロキサンは、本組成物の主剤(ベースポリマー)であって、該オルガノポリシロキサンとしては、下記平均組成式(II)で示されるものを用いることができる。
R3 aSiO(4-a)/2 ・・・(II)
(式中、R3は互いに同一又は異種の炭素数1~15、好ましくは1~10、より好ましくは1~8の非置換又は置換の一価炭化水素基であり、aは1.5~2.8、好ましくは1.8~2.5、より好ましくは1.95~2.05の範囲の正数である。)
なお、アルケニル基の含有量は、オルガノポリシロキサン中1.0×10-6mol/g~3.0×10-3mol/g、特に1.0×10-5mol/g~2.0×10-3mol/gとすることが好ましい。アルケニル基の量が1.0×10-6mol/gより少ないとゴム硬度が低すぎてゲル状になってしまう場合があり、また3.0×10-3mol/gより多いと架橋密度が高くなりすぎて、極端に硬度が高くなり、ゴムの弾性がなくなってしまう場合がある。このアルケニル基は、分子鎖末端のケイ素原子に結合していても、分子鎖途中(非末端)のケイ素原子に結合していても、両者に結合していてもよい。
R4 bHcSiO(4-b-c)/2 ・・・(III)
(式中、R4は互いに同一又は異種の炭素数1~15、好ましくは1~10、より好ましくは1~8の非置換又は置換の一価炭化水素基である。また、bは0.7~2.1、cは0.001~1.0で、かつb+cは0.8~3.0を満足する正数である。)
また、bは0.7~2.1、好ましくは0.8~2.0であり、cは0.001~1.0、好ましくは0.01~1.0であり、b+cは0.8~3.0、好ましくは1.0~2.5を満足する正数であり、オルガノハイドロジェンポリシロキサンの分子構造は、直鎖状、環状、分岐鎖状、三次元網目状のいずれの構造であってもよい。
また、(B)成分のオルガノハイドロジェンポリシロキサンとしては、上記で例示した化合物等において、分子を構成するシロキサン骨格(-Si-O-Si-)の一部(通常、シロキサン結合を形成する酸素原子の位置の一部)に、通常2~4価の、芳香族環含有の炭化水素骨格(例えば、フェニレン骨格、ビスフェニレン骨格、ビス(フェニレン)エーテル骨格、ビス(フェニレン)メタン骨格、2,2-ビス(フェニレン)プロパン骨格、2,2-ビス(フェニレン)ヘキサフルオロプロパン骨格など)を含有する、多価芳香族環含有のオルガノハイドロジェンポリシロキサンであってもよい。
なお、この白金触媒の配合量は触媒量とすることができ、通常、白金族金属(質量換算)として、(A)~(D)成分、後述する(E)成分を配合する場合は(A)~(E)成分の合計質量に対し、0.5~1,000ppm、特に1~500ppm程度である。
で示されるベンゾトリアゾール誘導体であり、上述した(C)成分の白金触媒と相互作用することにより、硬化後のシリコーンゴムの圧縮永久歪を低下させることができる。
分子鎖両末端がジメチルビニルシロキシ基で封鎖された平均重合度が750であるジメチルポリシロキサン(A1)100部、架橋剤として分子鎖両末端がトリメチルシロキシ基で封鎖され、側鎖にSiH基を有するメチルハイドロジェンポリシロキサン(B1)(重合度80、SiH基量0.0055mol/gの分子鎖両末端トリメチルシロキシ基封鎖ジメチルシロキサン・メチルハイドロジェンシロキサン共重合体)1.30部(SiH基/ビニル基=2.0mol/mol)、及び反応制御剤としてエチニルシクロヘキサノール0.05部を室温で15分間撹拌した。続いて、白金と1,3-ジビニル-1,1,3,3-テトラメチルジシロキサンの錯体のトルエン溶液(C1)(白金原子1質量%)を0.10部添加し、室温で15分撹拌し、シリコーンゴム配合物Aを得た。
実施例1のシリコーンゴム配合物A100部に対し、下記式で示されるベンゾトリアゾール誘導体(D2)
実施例1のシリコーンゴム配合物A100部に対し、下記式で示されるベンゾトリアゾール誘導体(D3)
実施例1のシリコーンゴム配合物A100部に対し、下記式で示されるベンゾトリアゾール誘導体(D4)
ベンゾトリアゾール誘導体を添加する前の実施例1のシリコーンゴム配合物Aの130℃における硬化性をレオメーターMDR2000(アルファテクノロジーズ社製)により測定した結果を表1に示した。また、シリコーンゴム配合物Aを120℃で15分間プレスキュアを行って得られた硬化物について、外観(色調)を目視で確認した結果、JIS-K6249に基づき、圧縮永久歪(圧縮率25%、温度150℃、試験時間22時間)を測定した結果、及び圧縮永久歪試験後のサンプルの外観(色調)を目視で確認した結果を表1に示した。
実施例1のシリコーンゴム配合物A100部に対し、ベンゾトリアゾールを0.005部(ベンゾトリアゾール/Pt原子=8.2mol/mol)を添加し、均一なシリコーンゴム組成物とした。該組成物の130℃における硬化性をレオメーターMDR2000(アルファテクノロジーズ社製)により測定した結果を表1に示した。また、該組成物を120℃で15分間プレスキュアを行って得られた硬化物について、外観(色調)を目視で確認した結果、JIS-K6249に基づき、圧縮永久歪(圧縮率25%、温度150℃、試験時間22時間)を測定した結果、及び圧縮永久歪試験後のサンプルの外観(色調)を目視で確認した結果を表1に示した。
実施例1のシリコーンゴム配合物A100部に対し、下記式で示されるベンゾトリアゾール誘導体(D5)
分子鎖両末端がジメチルビニルシロキシ基で封鎖された平均重合度が750であるジメチルポリシロキサン(A1)60部、BET法による比表面積が300m2/gであるヒュームドシリカ(E1)(日本アエロジル社製、アエロジル300)40部、ヘキサメチルジシラザン8部、及び水2.0部を室温で30分混合後、150℃に昇温し、3時間撹拌を続け、冷却し、シリコーンゴムベースを得た。
このシリコーンゴムベース100部に、上記ジメチルポリシロキサン(A1)40部、分子鎖両末端がトリメチルシロキシ基で封鎖され側鎖(即ち、主鎖を構成するジオルガノシロキサン単位中のケイ素原子に結合した一価の基又は原子、以下、同様。)のメチル基の2.5mol%がビニル基である平均重合度200のジメチルポリシロキサン(A2)5部、架橋剤として分子鎖両末端がトリメチルシロキシ基で封鎖され、側鎖にSiH基を有するメチルハイドロジェンポリシロキサン(B2)(重合度27、SiH基量0.0069mol/gの分子鎖両末端トリメチルシロキシ基封鎖ジメチルシロキサン・メチルハイドロジェンシロキサン共重合体)1.79部(SiH基/ビニル基=1.8mol/mol)、及び反応制御剤としてエチニルシクロヘキサノール0.12部を添加し、15分撹拌した。次いで白金と1,3-ジビニル-1,1,3,3-テトラメチルジシロキサンの錯体のトルエン溶液(C1)(白金原子1質量%)0.10部を添加し、30分間撹拌して均一なシリコーンゴム配合物Bを得た。
実施例5のシリコーンゴム配合物B100部に対し、実施例2のベンゾトリアゾール誘導体(D2)を0.009部(ベンゾトリアゾール誘導体/Pt原子=11.8mol/mol)を添加し、均一なシリコーンゴム組成物とした。該組成物の130℃における硬化性をレオメーターMDR2000(アルファテクノロジーズ社製)により測定した結果を表2に示した。また、該組成物を120℃で15分間プレスキュアを行って得られた硬化物について、外観(色調)を目視で確認した結果、JIS-K6249に基づき、圧縮永久歪(圧縮率25%、温度150℃、試験時間22時間)を測定した結果、及び圧縮永久歪試験後のサンプルの外観(色調)を目視で確認した結果を表2に示した。
実施例5のシリコーンゴム配合物B100部に対し、実施例3のベンゾトリアゾール誘導体(D3)を0.0135部(ベンゾトリアゾール誘導体/Pt原子=11.9mol/mol)を添加し、均一なシリコーンゴム組成物とした。該組成物の130℃における硬化性をレオメーターMDR2000(アルファテクノロジーズ社製)により測定した結果を表2に示した。また、該組成物を120℃で15分間プレスキュアを行って得られた硬化物について、外観(色調)を目視で確認した結果、JIS-K6249に基づき、圧縮永久歪(圧縮率25%、温度150℃、試験時間22時間)を測定した結果、及び圧縮永久歪試験後のサンプルの外観(色調)を目視で確認した結果を表2に示した。
実施例5のシリコーンゴム配合物B100部に対し、実施例4のベンゾトリアゾール誘導体(D4)を0.0225部(ベンゾトリアゾール誘導体/Pt原子=12.9mol/mol)を添加し、均一なシリコーンゴム組成物とした。該組成物の130℃における硬化性をレオメーターMDR2000(アルファテクノロジーズ社製)により測定した結果を表2に示した。また、該組成物を120℃で15分間プレスキュアを行って得られた硬化物について、外観(色調)を目視で確認した結果、JIS-K6249に基づき、圧縮永久歪(圧縮率25%、温度150℃、試験時間22時間)を測定した結果、及び圧縮永久歪試験後のサンプルの外観(色調)を目視で確認した結果を表2に示した。
実施例5のシリコーンゴム配合物B100部に対し、実施例3のベンゾトリアゾール誘導体(D3)を0.10部(ベンゾトリアゾール誘導体/Pt原子=88mol/mol)を添加し、均一なシリコーンゴム組成物とした。該組成物の130℃における硬化性をレオメーターMDR2000(アルファテクノロジーズ社製)により測定した結果を表2に示した。また、該組成物を120℃で15分間プレスキュアを行って得られた硬化物について、外観(色調)を目視で確認した結果、JIS-K6249に基づき、圧縮永久歪(圧縮率25%、温度150℃、試験時間22時間)を測定した結果、及び圧縮永久歪試験後のサンプルの外観(色調)を目視で確認した結果を表2に示した。
ベンゾトリアゾール誘導体を添加する前の実施例5のシリコーンゴム配合物Bの130℃における硬化性をレオメーターMDR2000(アルファテクノロジーズ社製)により測定した結果を表2に示した。また、シリコーンゴム配合物Bを120℃で15分間プレスキュアを行って得られた硬化物について、外観(色調)を目視で確認した結果、JIS-K6249に基づき、圧縮永久歪(圧縮率25%、温度150℃、試験時間22時間)を測定した結果、及び圧縮永久歪試験後のサンプルの外観(色調)を目視で確認した結果を表2に示した。
実施例5のシリコーンゴム配合物B100部に対し、ベンゾトリアゾールを0.005部(ベンゾトリアゾール/Pt原子=12.0mol/mol)を添加し、均一なシリコーンゴム組成物とした。該組成物の130℃における硬化性をレオメーターMDR2000(アルファテクノロジーズ社製)により測定した結果を表2に示した。また、該組成物を120℃で15分間プレスキュアを行って得られた硬化物について、外観(色調)を目視で確認した結果、JIS-K6249に基づき、圧縮永久歪(圧縮率25%、温度150℃、試験時間22時間)を測定した結果、及び圧縮永久歪試験後のサンプルの外観(色調)を目視で確認した結果を表2に示した。
Claims (6)
- (E)成分として、補強性充填剤を(A)成分100質量部に対して1~100質量部含有する請求項1又は2記載の付加硬化性シリコーンゴム組成物。
- (E)成分がBET法における比表面積が50m2/g以上のヒュームドシリカである請求項3記載の付加硬化性シリコーンゴム組成物。
- 130℃における2分測定時の10%硬化時間をT10、90%硬化時間をT90としたとき、T90-T10が40秒以下となるものである請求項1~4のいずれか1項記載の付加硬化性シリコーンゴム組成物。
- 請求項1~5のいずれか1項記載のシリコーンゴム組成物を硬化してなり、圧縮率25%、150℃で22時間圧縮後の圧縮永久歪が30%以下であるシリコーンゴム硬化物。
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WO2017159047A1 (ja) * | 2016-03-18 | 2017-09-21 | 信越化学工業株式会社 | 付加硬化性シリコーンゴム組成物及び硬化物 |
WO2018079309A1 (ja) * | 2016-10-26 | 2018-05-03 | 信越化学工業株式会社 | 熱伝導性シリコーン組成物 |
WO2022163365A1 (ja) * | 2021-01-27 | 2022-08-04 | 信越化学工業株式会社 | オイルブリード性シリコーンゴム組成物 |
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JP2019031601A (ja) * | 2017-08-07 | 2019-02-28 | 信越化学工業株式会社 | 付加硬化型シリコーン組成物及びシリコーンゴム硬化物 |
CN111868173B (zh) * | 2018-03-12 | 2022-11-01 | 莫门蒂夫性能材料有限责任公司 | 低压缩永久变形的硅橡胶组合物 |
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CN112218914B (zh) * | 2018-05-24 | 2022-11-22 | 莫门蒂夫性能材料股份有限公司 | 渗油性自粘合液体有机硅橡胶组合物 |
JP2020111670A (ja) * | 2019-01-11 | 2020-07-27 | 信越化学工業株式会社 | 付加硬化型自己接着性シリコーンゴム組成物及びシリコーンゴム硬化物 |
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EP3309219A1 (en) | 2018-04-18 |
CN107636078A (zh) | 2018-01-26 |
US20180134871A1 (en) | 2018-05-17 |
EP3309219A4 (en) | 2018-12-26 |
EP3309219B1 (en) | 2019-07-24 |
JP2017002165A (ja) | 2017-01-05 |
JP6572634B2 (ja) | 2019-09-11 |
KR20180016392A (ko) | 2018-02-14 |
TW201713716A (zh) | 2017-04-16 |
US10544281B2 (en) | 2020-01-28 |
TWI713535B (zh) | 2020-12-21 |
CN107636078B (zh) | 2020-11-13 |
KR102313596B1 (ko) | 2021-10-19 |
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