WO2015093139A1 - 多成分系室温硬化性オルガノポリシロキサン組成物、該組成物の硬化物及び該硬化物からなる成型物 - Google Patents
多成分系室温硬化性オルガノポリシロキサン組成物、該組成物の硬化物及び該硬化物からなる成型物 Download PDFInfo
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- C09D183/00—Coating compositions based on 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; Coating compositions based on derivatives of such polymers
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- C09D183/00—Coating compositions based on 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; Coating compositions based on derivatives of such polymers
- C09D183/14—Coating compositions based on 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; Coating compositions based on 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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- C09J183/00—Adhesives based on 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; Adhesives based on derivatives of such polymers
- C09J183/04—Polysiloxanes
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- C09J183/00—Adhesives based on 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; Adhesives based on derivatives of such polymers
- C09J183/14—Adhesives based on 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; Adhesives based on 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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Definitions
- the present invention relates to a room temperature curable organopolysiloxane composition, a cured product of the composition, and a molded product comprising the cured product, and in particular, as a main agent (base polymer), an alkoxysilyl-ethylene group is blocked at the terminal.
- Composition especially multi-component room temperature curable organopolysiloxane composition
- cured product and molded product especially silicone rubber cured product, silicone rubber molded product
- room temperature curable organopolysiloxane compositions that is, room temperature curable silicone rubber compositions
- elastomeric (rubber-like elastic body) at room temperature upon contact with moisture in the air have various curing types.
- dealcoholation type are characterized by no unpleasant odor and no corrosion of metals.
- sealing and bonding of electrical and electronic equipment It is preferably used for coating.
- compositions comprising a hydroxyl-terminated polyorganosiloxane, an alkoxysilane and an organotitanium compound, a composition comprising an alkoxysilyl end-capped polyorganosiloxane, an alkoxysilane and an alkoxytitanium, and an alkoxy containing a silethylene group.
- a composition comprising a linear polyorganosiloxane blocked with a silyl end, an alkoxysilane and an alkoxytitanium, and further comprising a hydroxyl endblocked polyorganosiloxane or an alkoxy endblocked polyorganosiloxane and an alkoxy- ⁇ -silyl ester compound. Examples thereof include compositions (Patent Documents 1 to 4).
- compositions have a certain degree of storage stability, water resistance and moisture resistance, but have not fully satisfied these. Furthermore, the fast curability is still insufficient.
- polymers having a reactive alkoxysilyl group at the terminal are conventionally known. Since the polymer terminal group is previously blocked with an alkoxysilyl group, this polymer is less likely to change (decrease) in curability over time and has excellent storage stability.
- workability viscosity and thixotropy
- the dealcohol type is low in reactivity with moisture in the air, so the curability is insufficient. there were.
- an object of the present invention is to provide a room temperature curable polyorganosiloxane composition capable of providing a cured product excellent in rapid curability and excellent in storage stability and durability, in particular, a silicone rubber cured product. There is to do.
- the silicon compound such as an organopolysiloxane having an alkoxysilyl-ethylene group at the end represented by the following structural formula (1), which has been found to be improved, includes an organopolysiloxane having both molecular chains blocked with silanol groups.
- room temperature curable composition that gives a cured product that is particularly excellent in fast curability and at the same time has good storage stability and durability, especially room temperature curable that gives a cured silicone rubber product
- the inventors have found that an organopolysiloxane composition can be obtained and completed the present invention. That is, the present invention provides the following room temperature curable organopolysiloxane composition and cured product.
- R 1 is an optionally substituted alkyl group having 1 to 20 carbon atoms, and the alkyl group having 3 or more carbon atoms may be a cyclic cycloalkyl group.
- R 2 is an optionally substituted hydrocarbon group having 1 to 20 carbon atoms, a is an integer of 1 to 3, and n is an integer of 0 to 10.
- (B) Organopolysiloxane represented by the following general formula (2) (A) 10 to 250 parts by mass with respect to 100 parts by mass of component,
- R 2 is an optionally substituted hydrocarbon group having 1 to 20 carbon atoms.
- M is a number that makes the viscosity of the organopolysiloxane at 25 ° C. 10 to 1,000,000 mPa ⁇ s.
- Curing catalyst (A) 0.001 to 20 parts by mass with respect to 100 parts by mass of component, A room temperature-curable organopolysiloxane composition comprising:
- the component (A) is at least one alkoxysilyl-ethylene group-terminated organopolysiloxane selected from diorganopolysiloxanes represented by the following general formulas (A) and (B) ⁇ 2 > The room temperature curable organopolysiloxane composition described.
- R 1 is 20 alkyl group from carbon atoms 1 may have a substituent, may .
- R 2 also has 3 or more carbon atoms a cycloalkyl group of the alkyl group A monovalent hydrocarbon group having 1 to 20 carbon atoms which may have a substituent, a is an integer of 1 to 3, n is an integer of 0 to 10, and l and m are each an integer of 0 to 2000 .
- the composition further comprises at least one component selected from the following (D) to (G) with respect to 100 parts by mass of component (A): A room temperature curable organopolysiloxane composition.
- R 2 is an optionally substituted hydrocarbon group having 1 to 20 carbon atoms.
- M is an integer of 1 to 2000
- Organopolysiloxane composition I containing component (A), component (C), and optionally component (G) and / or component (E), component (B) and component (D) and / or component if necessary.
- a sealing agent, coating agent, or adhesive comprising the room temperature-curable organopolysiloxane composition described in any one of the above items.
- ⁇ 8> A cured product of the room temperature curable organopolysiloxane composition according to any one of ⁇ 1> to ⁇ 6>.
- the room temperature curable organopolysiloxane composition of the present invention is particularly excellent in preservability and fast curability, and further rapidly cures when exposed to air, for example, even after storage for 12 months, particularly 6 months, It becomes a cured product such as silicone rubber having excellent physical properties.
- the composition of the present invention is useful as a sealant, a coating agent, and an adhesive where heat resistance, water resistance, and moisture resistance are required. It is useful as an adhesive application.
- the component (A) is an alkoxysilyl-ethylene group-terminated organopolysiloxane having at least one group represented by the following structural formula (1) (that is, an alkoxysilyl-ethylene group-containing triorganosiloxy group) in the molecule. .
- R 1 is an optionally substituted alkyl group having 1 to 20 carbon atoms, and the alkyl group having 3 or more carbon atoms may be a cyclic cycloalkyl group.
- R 2 is an optionally substituted hydrocarbon group having 1 to 20 carbon atoms, a is an integer of 1 to 3, and n is an integer of 0 to 10.
- the alkoxysilyl-ethylene group-terminated organopolysiloxane having at least one group represented by the structural formula (1) in the component (A) is used as a main agent (base polymer) of the composition of the present invention.
- the main chain basically consists of a repeating structure of diorganosiloxane units, and both ends of the molecular chain are blocked with triorganosiloxy groups.
- the diorganopolysiloxane is preferably.
- the group represented by the structural formula (1) that is, the alkoxysilyl-ethylene group-containing triorganosiloxy group
- the organopolysiloxane of component (A) is at least It is desirable from the viewpoint of fast curability that it contains one each at both ends of the molecular chain (at least two in the molecule). Accordingly, the organopolysiloxane of component (A) is a linear diorganopolysiloxane containing at least one group represented by the structural formula (1) at both ends of the molecular chain.
- a linear diorganopolysiloxane containing only one group represented by (1) at both ends of the molecular chain (that is, only two in total at both ends of the molecular chain) is desirable.
- Particularly preferred are diorganopolysiloxanes represented by the following general formula (A) and / or (B).
- R 1 is an alkyl group having 1 to 20 carbon atoms, preferably 1 to 10 carbon atoms, more preferably 1 to 4 carbon atoms (unsubstituted or substituted alkyl group) which may have a substituent.
- the alkyl group having 3 or more carbon atoms may be a cyclic cycloalkyl group, and R 2 may have a substituent and has 1 to 20 carbon atoms, preferably 1 carbon atom.
- a is an integer of 1 to 3, preferably 2 or 3, more preferably 3.
- n is 0 to 10.
- l and m are each an integer of 0 to 2000, preferably l is 0.
- An integer of ⁇ 20, m is an integer of 10 to 2000, more preferably l is 0 10 integer, m is a 40-1500 integer, more preferably, l is 0, m is an integer of 100-1000.
- the alkyl group having 1 to 20 carbon atoms which may have a substituent of R 1 includes methyl group, ethyl group, propyl group, isopropyl group, butyl Group, isobutyl group, tert-butyl group, pentyl group, hexyl group, heptyl group, octyl group, 2-ethylhexyl group, nonyl group, decyl group, octadecyl group and other alkyl groups; cyclopentyl group, cyclohexyl group and other cycloalkyl groups Aralkyl groups such as benzyl group, 2-phenylethyl group and 3-phenylpropyl group; some or all of the hydrogen atoms of these groups are halogen atoms such as F, Cl and Br, cyano groups and alkoxy groups; Groups substituted with, for example, 3-chloro
- Examples of the hydrolyzable group OR 1 (alkoxy group) at the terminal in the formula (1) include methoxy group, ethoxy group, propoxy group, isopropoxy group, butoxy group, isobutoxy group, tert-butoxy group, 2- Examples thereof include alkoxy groups such as ethylhexoxy group; alkoxyalkoxy groups such as methoxyethoxy group, ethoxyethoxy group and methoxypropoxy group. Among these, a methoxy group and an ethoxy group are particularly preferable because of their fast curability.
- Examples of the substituted or unsubstituted monovalent hydrocarbon group for R 2 include a methyl group, an ethyl group, a propyl group, an isopropyl group, a butyl group, an isobutyl group, a tert-butyl group, a pentyl group, a hexyl group, a heptyl group, and an octyl group.
- Alkyl groups such as 2-ethylhexyl group, nonyl group, decyl group and octadecyl group; cycloalkyl groups such as cyclopentyl group and cyclohexyl group; alkenyl groups such as vinyl group, allyl group, butenyl group, pentenyl group and hexenyl group; phenyl Aryl groups such as a group, tolyl group, xylyl group, ⁇ -, ⁇ -naphthyl group; aralkyl groups such as benzyl group, 2-phenylethyl group, 3-phenylpropyl group; and a part of hydrogen atoms of these groups Or a group in which all are substituted with a halogen atom such as F, Cl, Br or a cyano group, such as a 3-chloropropyl group, 3, Examples thereof include 3,3-trifluoropropyl group and 2-cyanoethyl
- the diorganopolysiloxane as component (A) preferably has a viscosity at 25 ° C. of 10 to 1,000,000 mPa ⁇ s, more preferably 50 to 500,000 mPa ⁇ s, and particularly preferably 100 to 100,000 mPa ⁇ s. s, especially 1000 to 80,000 mPa ⁇ s. If the viscosity of the diorganopolysiloxane is 10 mPa ⁇ s or more, it is easy to obtain a coating film having excellent physical and mechanical strength. If the viscosity is 1,000,000 mPa ⁇ s or less, the composition This is preferable because the viscosity of the resin does not become too high and the workability during use is good.
- the viscosity is a numerical value measured by a rotational viscometer (for example, BL type, BH type, BS type, cone plate type, rheometer, etc.).
- a rotational viscometer for example, BL type, BH type, BS type, cone plate type, rheometer, etc.
- disiloxane having ethynyl groups at both ends and octamethylcyclotetrasiloxane are polymerized to produce a diorganopolysiloxane having ethynyl groups at both ends.
- the viscosity can be decreased by increasing the amount of disiloxane having an ethynyl group, and the viscosity can be increased by decreasing the amount of disiloxane having an ethynyl group. What is necessary is just to adjust the compounding quantity of disiloxane which has this.
- the diorganopolysiloxane of the component (A) is, for example, a diorganopolysiloxane having acetylene groups at both ends and octamethylcyclotetrasiloxane polymerized in a sulfuric acid catalyst and having ethynyl groups at both ends. It can be produced by producing siloxane and then adding trialkoxysilane.
- Examples of the addition reaction catalyst used for adding trialkoxysilane include platinum group metal catalysts such as platinum, palladium, and rhodium, with platinum being particularly preferred.
- platinum-based material include platinum black, alumina, silica, or the like supported on solid platinum, chloroplatinic acid, alcohol-modified chloroplatinic acid, a complex of chloroplatinic acid and olefin, or platinum and vinylsiloxane. And the like can be exemplified.
- These catalysts may be used in so-called catalytic amounts. For example, they are used in an amount of 0.1 to 1,000 ppm, particularly 0.5 to 100 ppm in terms of platinum group metal with respect to trialkoxysilanes.
- This reaction is preferably carried out at a temperature of 50 to 120 ° C., particularly 60 to 100 ° C., for 0.5 to 12 hours, particularly 1 to 6 hours, and can be carried out without using a solvent.
- an appropriate solvent such as toluene or xylene can be used if necessary.
- (A) component diorganopolysiloxane examples include the following.
- diorganopolysiloxane of component (A) can be used singly or in combination of two or more having different structures and molecular weights.
- the organopolysiloxane of component (B) is a linear diorganopolysiloxane represented by the following structural formula (2), in which both ends of the molecular chain are blocked with silanol groups (hydroxyl groups bonded to silicon atoms), When used together with the organopolysiloxane of the component (A) at a specific ratio, it functions as the main agent (base polymer) of the composition of the present invention.
- R 2 is a monovalent hydrocarbon group having 1 to 20 carbon atoms, preferably 1 to 8 carbon atoms which may have a substituent (unsubstituted or substituted monovalent hydrocarbon group). Is a number that makes the viscosity of the organopolysiloxane at 25 ° C.
- the substituted or unsubstituted monovalent hydrocarbon group represented by R 2 is methyl group, ethyl group, propyl group, isopropyl group, butyl group, isobutyl group, tert-butyl group, pentyl group, hexyl.
- the organopolysiloxane of component (B) preferably has a viscosity at 25 ° C. of 10 to 1,000,000 mPa ⁇ s, more preferably 50 to 500,000 mPa ⁇ s, particularly preferably 100 to 100,000 mPa ⁇ s. ⁇ S, especially 100 to 80,000 mPa ⁇ s. If the organopolysiloxane has a viscosity of 10 mPa ⁇ s or more, it is easy to obtain a coating film excellent in physical and mechanical strength. If the viscosity is 1,000,000 mPa ⁇ s or less, the composition of This is preferable because the viscosity does not become too high and the workability during use is good.
- the viscosity is a numerical value measured by a rotational viscometer.
- the blending amount of the component (B) is in the range of 10 to 250 parts by mass, more preferably 15 to 150 parts by mass with respect to 100 parts by mass of the component (A). If it exceeds 250 parts by mass, satisfactory curability may not be obtained.
- the component (B) can be prepared as a separate composition from the component (A), and a multi-component composition composed of two or more (two-component) compositions can be uniformly mixed during use. preferable.
- the component (C) is a curing catalyst and is used for curing the composition.
- curing catalysts include dibutyltin diacetate, dibutyltin dilaurate, dioctyltin dilaurate, and alkyltin ester compounds such as dibutyltin dioctoate, tetraisopropoxy titanium, tetra n-butoxy titanium, tetrakis (2-ethylhexoxy) titanium, dipropoxy bis (Acetylacetonato) titanium, titanium isopropoxyoctylene glycol, etc.
- titanate or titanium chelate compound zinc naphthenate, zinc stearate, zinc-2-ethyl octoate, iron-2-ethylhexoate, cobalt- Alcolate aluminum compounds such as 2-ethylhexoate, manganese-2-ethylhexoate, cobalt naphthenate, aluminum isopropylate, aluminum secondary butyrate, aluminum
- Aluminum chelate compounds such as um alkyl acetate, diisopropylate, aluminum bisethyl acetoacetate, monoacetylacetonate, bismuth (III) neodecanoate, bismuth (III) 2-ethylhexanoate, bismuth (III) citrate, octylic acid Organometallic compounds such as bismuth; Phosphazene-containing compounds, aminoalkyl group-substituted alkoxysilanes such as 3-aminopropyltriethoxysilane, N-
- Amine compounds or salts thereof quaternary ammonium salts such as benzyltriethylammonium acetate; lower fatty acid salts of alkali metals such as potassium acetate, sodium acetate, lithium oxalate; dimethylhydroxylamine, die Silanes containing guanidyl groups such as tetramethylguanidylpropyltrimethoxysilane, tetramethylguanidylpropylmethyldimethoxysilane, tetramethylguanidylpropyltris (trimethylsiloxy) silane, and the like; Although siloxane etc. are illustrated, (C) component is not limited to these. The component (C) may be used alone or in combination of two or more.
- the blending amount of the component (C) is 0.001 to 20 parts by weight, particularly preferably 0.005 to 10 parts by weight with respect to 100 parts by weight of the component (A).
- hydrolyzable silane and / or its partially hydrolyzed condensate acts as a crosslinking agent.
- hydrolyzable silanes examples include tetraalkoxysilanes and alkyltrialkoxysilanes.
- trifunctional or tetrafunctional organoxysilanes such as alkyltri (alkoxy-substituted alkoxy) silane and alkyltrialkenyloxysilane can be exemplified.
- ethyl silicate propyl silicate, tetraethoxysilane, tetrapropoxysilane, methyltrimethoxysilane, methyltriethoxysilane, ethyltrimethoxysilane, ethyltriethoxysilane, methyltris (methoxyethoxy) silane, ethyltris.
- the blending amount is usually 0.1 to 30 parts by mass with respect to 100 parts by mass of the component (A), but it should be 0.2 to 20 parts by mass. Preferably, it is 0.5 to 15 parts by mass. If the blending amount exceeds 30 parts by mass, there may be a problem that the cured product becomes too hard or economically disadvantageous.
- the room temperature curable organopolysiloxane composition of the present invention is preferably stored separately from the above components (A) to (D) as two compositions from the viewpoint of storage stability (so-called two-component).
- the organosiloxane composition II in which the component (B) and the necessary component (D) are mixed in advance, and the organopolysiloxane composition I and the organopolysiloxane composition II are mixed immediately before actual use to prepare a room temperature curable organo A siloxane composition is preferred.
- other components may be optionally added.
- the organopolysiloxane composition IV may thicken when stored for a long period of time, it is preferable to use the two compositions I and II. As long as the components (A) and (B) are known, other components may be optionally added. Further, one or more selected from the following (E) component, (F) component, and (G) component, or one or more selected from organosiloxane composition I to organosiloxane composition IV. It can be arbitrarily blended in the composition.
- -(E) component- Component (E) is a filler (inorganic filler and / or organic resin filler), and is used to give sufficient mechanical strength to a cured product formed from this composition.
- Known fillers can be used, for example, finely divided silica, fumed silica, precipitated silica, silica whose surface is hydrophobized with an organosilicon compound, glass beads, glass balloons, transparent Resin beads, silica airgel, diatomaceous earth, iron oxide, zinc oxide, titanium oxide, metal oxides such as fumed metal oxide, wet silica or those whose surfaces are treated with silane, quartz powder, carbon black, talc, zeolite and Reinforcing agents such as bentonite, metal carbonates such as asbestos, glass fiber, carbon fiber, calcium carbonate, magnesium carbonate, zinc carbonate, synthesis of asbestos, glass wool, fine mica, fused silica powder, polystyrene, polyvinyl chloride, polypropylene, etc.
- Resin powder or the like is used.
- these fillers silica, calcium carbonate, zeolite, and the like are preferable, and fumed silica and calcium carbonate whose surfaces have been subjected to a hydrophobic treatment are particularly preferable.
- the blending amount is preferably 1 to 1000 parts by weight, particularly preferably 1 to 400 parts by weight, per 100 parts by weight of the component (A).
- the blending amount is preferably 1 to 1000 parts by weight, particularly preferably 1 to 400 parts by weight, per 100 parts by weight of the component (A).
- -(F) component- Component (F) is an adhesion promoter and is used to give sufficient adhesion to a cured product formed from this composition.
- an adhesion promoter for example, a silane coupling agent such as alkoxysilane having a functional group-containing monovalent hydrocarbon group (so-called carbon functional silane)
- a known one is preferably used, and a vinylsilane coupling agent, (Meth) acrylic silane coupling agent, epoxy silane coupling agent, amino silane silane coupling agent, mercapto silane coupling agent, etc.
- vinyl trimethoxy silane vinyl triethoxy silane
- vinyl tripropenoxy Alkenyltriorganoxysilanes such as silane, vinyltris ( ⁇ -methoxyethoxy) silane, ⁇ -methacryloxypropyltrimethoxysilane, ⁇ - (3,4-epoxycyclohexyl) ethyltrimethoxysilane, ⁇ -glycidoxypropyltri Toxisilane, ⁇ -glycidoxypropylmethyldiethoxysilane, N- ⁇ - (aminoethyl) ⁇ -aminopropyltrimethoxysilane, ⁇ -aminopropyltriethoxysilane, 3-2- (aminoethylamino) propyltrimethoxysilane And ⁇ -mercaptopropyltrimethoxysilane, isocyanate silane and the like.
- aminosilanes such as ⁇ -aminopropyltriethoxysilane, 3-2- (aminoethylamino) propyltrimethoxysilane, ⁇ -glycidoxypropyltrimethoxysilane, ⁇ - (3,4-epoxycyclohexyl) ethyltrimethoxy
- Epoxy silanes such as silane, isocyanate silane and the like are preferable.
- the blending amount is preferably 0.1 to 30 parts by weight, particularly 0.1 to 20 parts by weight, based on 100 parts by weight of the component (A).
- the blending amount is preferably 0.1 to 30 parts by weight, particularly 0.1 to 20 parts by weight, based on 100 parts by weight of the component (A).
- the organopolysiloxane of component (G) can be involved in hydrolysis condensation / crosslinking (curing) reactions such as components (A) and (B) in the molecule represented by the following general formula (3). It is a so-called non-functional linear diorganopolysiloxane (silicone oil component) that does not contain a functional group, and acts as a diluent for the composition of the present invention, if necessary.
- R 2 is a monovalent hydrocarbon group having 1 to 20 carbon atoms, preferably 1 to 8 carbon atoms which may have a substituent (unsubstituted or substituted monovalent hydrocarbon group). Is an integer of 1 to 2000, preferably an integer of 10 to 2000, more preferably an integer of 40 to 1500, and still more preferably an integer of about 100 to 1000.
- the substituted or unsubstituted monovalent hydrocarbon group for R 2 is methyl group, ethyl group, propyl group, isopropyl group, butyl group, isobutyl group, tert-butyl group, pentyl group, hexyl.
- the organopolysiloxane of component (G) preferably has a viscosity at 25 ° C. of 0.65 to 1,000,000 mPa ⁇ s, more preferably 30 to 500,000 mPa ⁇ s, and particularly preferably 50 to 100. 3,000 mPa ⁇ s, particularly 100 to 80,000 mPa ⁇ s is preferable. If the organopolysiloxane has a viscosity of 10 mPa ⁇ s or more, it is easy to obtain a coating film excellent in physical and mechanical strength. If the viscosity is 1,000,000 mPa ⁇ s or less, the composition of This is preferable because the viscosity does not become too high and the workability during use is good. Here, the viscosity is a numerical value measured by a rotational viscometer.
- the blending amount is preferably 1 to 100 parts by weight, more preferably 5 to 70 parts by weight, with respect to 100 parts by weight of the component (A). More preferably, the amount is ⁇ 60 parts by mass.
- the viscosity of a composition is low and sufficient workability
- operativity is obtained, it is not necessary to add, and when it exceeds 100 mass parts, rubber
- the room temperature curable organopolysiloxane composition of the present invention further includes, as optional additives, flame retardants such as pigments, dyes, anti-aging agents, antioxidants, antistatic agents, antimony oxide, and paraffin chloride.
- flame retardants such as pigments, dyes, anti-aging agents, antioxidants, antistatic agents, antimony oxide, and paraffin chloride.
- Known additives can be blended.
- a polyether as a thixotropy improver, a fungicide, and an antibacterial agent can be blended.
- the room temperature curable organopolysiloxane composition of the present invention can be obtained by uniformly mixing the above-described components and further predetermined amounts of the above-mentioned various additives in a dry atmosphere.
- the room temperature curable organopolysiloxane composition is cured by allowing it to stand at room temperature, and the molding method, curing conditions, and the like can employ known methods and conditions according to the type of the composition. .
- the room temperature curable organopolysiloxane composition of the present invention thus obtained is rapidly cured at room temperature by moisture in the air, heat resistance, water resistance, moisture resistance, weather resistance, low temperature characteristics, various substrates, particularly metals.
- a cured rubber elastic body having excellent adhesion to the resin is formed.
- the composition of the present invention is particularly excellent in storage stability and curability, for example, rapidly cured when exposed to the air after storage for 12 months, particularly 6 months, and has excellent physical properties as described above.
- this composition does not cause contact failure of electrical and electronic parts, it is useful as an insulating material and adhesive for electrical and electronic parts, as well as a sealing agent, coating agent, coating agent for various substrates, It can be widely used as a release treatment agent and also as a fiber treatment agent. Further, the composition can be cured and molded to obtain various molded products, and the molded products have excellent heat resistance, water resistance, moisture resistance, weather resistance, and the like.
- part means “part by mass”
- Me represents a methyl group.
- the viscosity is a value measured by a rotational viscometer at 25 ° C.
- Example 1 As a first component, 100 parts by mass of Polymer B was mixed with 0.5 part of dioctyltin dilaurate under reduced pressure until uniform, thereby obtaining Composition I. As a second component, 100 parts by mass of linear dimethylpolysiloxane (viscosity of 5000 mPa ⁇ s at 25 ° C.) blocked with hydroxyl groups at both ends of the molecular chain was used as Composition II. Composition I and Composition II were mixed under moisture barrier to prepare room temperature curable organopolysiloxane composition 1.
- Example 2 As a first component, 0.25 part of tetramethylguanidylpropyltrimethoxysilane was mixed with 100 parts by weight of polymer B under reduced pressure until uniform, thereby obtaining Composition I. As a second component, 100 parts by mass of linear dimethylpolysiloxane (viscosity of 5000 mPa ⁇ s at 25 ° C.) blocked with hydroxyl groups at both ends of the molecular chain was used as Composition II. Composition I and Composition II were mixed under moisture barrier to prepare room temperature curable organopolysiloxane composition 2.
- Example 3 As a first component, 100 parts by mass of Polymer B was mixed with 0.51 part of bismuth (III) neodecanoate until uniform under reduced pressure to obtain Composition I. As a second component, 100 parts by mass of linear dimethylpolysiloxane (viscosity of 5000 mPa ⁇ s at 25 ° C.) blocked with hydroxyl groups at both ends of the molecular chain was used as Composition II. Composition I and Composition II were mixed under moisture barrier to prepare room temperature curable organopolysiloxane composition 3.
- each composition prepared in Examples 1 to 3 and Comparative Examples 1 to 6 was measured. Further, each composition immediately after the preparation prepared in Examples 1 to 3 and Comparative Examples 1 to 6 was extruded into a sheet having a thickness of 2 mm, and was put into air at 23 ⁇ 2 ° C. and 50 ⁇ 5% RH (relative humidity). Next, the physical properties (initial physical properties) of a cured product obtained by exposing the sheet to the same atmosphere for 3 days were measured according to JIS K-6249. The hardness was measured using a durometer A hardness meter of JIS K-6249. Further, the cured product was stored in a constant temperature and humidity chamber at 85 ° C.
- Example 4 As a first component, 100 parts by mass of polymer B, 13 parts of a filler (a fumed silica whose surface was hydrophobized with dimethylchlorosilane), and both ends of a molecular chain having a viscosity of 100 mPa ⁇ s were blocked with trimethylsiloxy groups.
- a composition I was obtained by mixing 5 parts of linear dimethylpolysiloxane and 1 part of tetramethylguanidylpropyltrimethoxysilane until the mixture became homogeneous under reduced pressure.
- composition II 100 parts by mass of linear dimethylpolysiloxane (viscosity 5000 mPa ⁇ s at 25 ° C.) blocked with hydroxyl groups at both ends of the molecular chain, 5 parts of vinyltrimethoxysilane, 0.8 part of 3-aminopropyltriethoxysilane, 0.8 parts of N-2- (aminoethyl) -3-aminopropyltrimethoxysilane was mixed to obtain Composition II.
- Composition I and Composition II were mixed under moisture barrier to prepare room temperature curable organopolysiloxane composition 4.
- composition 7 was prepared in the same manner as in Example 4 except that 100 parts of linear dimethylpolysiloxane having both ends of a molecular chain having a viscosity of 1000 mPa ⁇ s blocked with trimethoxysilyl-ethane groups was used instead of polymer B. was prepared.
- composition 8 was prepared in the same manner as in Example 4 except that 100 parts of linear dimethylpolysiloxane having both ends of a molecular chain having a viscosity of 1000 mPa ⁇ s blocked with a trimethoxysiloxy group was used instead of the polymer B. did.
- each composition immediately after preparation prepared in Example 4 and Comparative Examples 7 and 8 was extruded into a sheet having a thickness of 2 mm, exposed to air at 23 ° C. and 50% RH, and then the sheet was subjected to the same atmosphere.
- the physical properties (initial physical properties) of the cured product obtained by allowing to stand for 3 days were measured according to JIS K-6249.
- the hardness was measured using a durometer A hardness meter of JIS K-6249.
- the cured product was stored in a constant temperature and humidity chamber at 85 ° C. and 85% RH for 7 days and measured in the same manner. Moreover, what heated this hardened
- the present invention is not limited to the above embodiment.
- the above-described embodiment is an exemplification, and the present invention has any configuration that has substantially the same configuration as the technical idea described in the claims of the present invention and that exhibits the same effects. Are included in the technical scope.
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Abstract
Description
即ち、本発明は、次の室温硬化性オルガノポリシロキサン組成物及び硬化物を提供するものである。
(A)下記構造式(1)で表される基を少なくとも分子中に1つ有するアルコキシシリル-エチレン基末端オルガノポリシロキサン
(B)下記一般式(2)で示されるオルガノポリシロキサン (A)成分100質量部に対して10~250質量部、
(C)硬化触媒 (A)成分100質量部に対して0.001~20質量部、
を含有することを特徴とする室温硬化性オルガノポリシロキサン組成物。
前記(A)成分の主鎖がジオルガノシロキサン単位の繰返しからなる直鎖状オルガノポリシロキサンであることを特徴とする<1>記載の室温硬化性オルガノポリシロキサン組成物。
前記(A)成分が下記一般式(A)及び式(B)で示されるジオルガノポリシロキサンから選ばれる少なくとも1種の前記アルコキシシリル-エチレン基末端オルガノポリシロキサンであることを特徴とする<2>記載の室温硬化性オルガノポリシロキサン組成物。
更に、(A)成分100質量部に対して、次の(D)~(G)から選ばれる1種以上の成分を下記質量部含有することを特徴とする<1>~<3>に記載の室温硬化性オルガノポリシロキサン組成物。
(D)加水分解性シラン及び/又はその部分加水分解縮物 0.1~30質量部
(E)充填剤 1~1000質量部
(F)接着促進剤 0.1~30質量部
(G)下記構造式で示されるオルガノポリシロキサン 1~100質量部
(A)成分と(C)成分と、必要により(G)成分及び/又は(E)成分とを含有するオルガノポリシロキサン組成物Iと、(B)成分と必要により(D)成分及び/又は(E)成分とを含有するオルガノシロキサン組成物IIからなる2液型であることを特徴とする<4>に記載の室温硬化性オルガノポリシロキサン組成物。
更に、(F)成分及び/又は(G)成分をオルガノシロキサン組成物I及び/又はオルガノシロキサン組成物IIに配合した<5>に記載の室温硬化性オルガノポリシロキサン組成物。
<1>~<6>の何れか1項に記載の室温硬化性オルガノポリシロキサン組成物を含有することを特徴とする、シール剤、コーティング剤又は接着剤。
<1>~<6>の何れか1項に記載の室温硬化性オルガノポリシロキサン組成物の硬化物。
<8>に記載の硬化物からなる成型物。
<室温硬化性オルガノポリシロキサン組成物>
-(A)成分-
(A)成分は、下記構造式(1)で表される基(即ち、アルコキシシリル-エチレン基含有トリオルガノシロキシ基)を少なくとも分子中に1つ有するアルコキシシリル-エチレン基末端オルガノポリシロキサンである。
とりわけ、下記一般式(A)及び/又は(B)で表わされるジオルガノポリシロキサンが好ましいものとして挙げられる。
(A)成分のジオルガノポリシロキサンは、1種単独でも構造や分子量の異なる2種以上を組み合わせても使用することができる。
(B)成分のオルガノポリシロキサンは、下記構造式(2)で示される、分子鎖両末端がシラノール基(ケイ素原子に結合した水酸基)で封鎖された直鎖状のジオルガノポリシロキサンであり、前記(A)成分のオルガノポリシロキサンと共に特定の比率で併用することによって本発明組成物の主剤(ベースポリマー)として作用するものである。
上記式(2)中、R2の置換又は非置換の一価炭化水素基としては、メチル基、エチル基、プロピル基、イソプロピル基、ブチル基、イソブチル基、tert-ブチル基、ペンチル基、ヘキシル基、ヘプチル基、オクチル基、2-エチルヘキシル基、ノニル基、デシル基、オクタデシル基等のアルキル基;シクロペンチル基、シクロヘキシル基等のシクロアルキル基;ビニル基、アリル基、ブテニル基、ペンテニル基、ヘキセニル基等のアルケニル基;フェニル基、トリル基、キシリル基、α-,β-ナフチル基等のアリール基;ベンジル基、2-フェニルエチル基、3-フェニルプロピル基等のアラルキル基;また、これらの基の水素原子の一部又は全部が、F、Cl、Br等のハロゲン原子やシアノ基等で置換された基、例えば、3-クロロプロピル基、3,3,3-トリフルオロプロピル基、2-シアノエチル基等を例示することができる。これらの中でも、メチル基、エチル基が好ましく、入手の容易さ、生産性、コストの面からメチル基が特に好ましい。
(C)成分は硬化触媒であり、組成物を硬化させるために使用される。硬化触媒としては、ジブチル錫ジアセテート、ジブチル錫ジラウレート、ジオクチル錫ジラウレート、ジブチル錫ジオクトエート等のアルキル錫エステル化合物、テトライソプロポキシチタン、テトラn-ブトキシチタン、テトラキス(2-エチルヘキソキシ)チタン、ジプロポキシビス(アセチルアセトナト)チタン、チタニウムイソプロポキシオクチレングリコール等のチタン酸エステル又はチタンキレート化合物、ナフテン酸亜鉛、ステアリン酸亜鉛、亜鉛-2-エチルオクトエート、鉄-2-エチルヘキソエート、コバルト-2-エチルヘキソエート、マンガン-2-エチルヘキソエート、ナフテン酸コバルト、アルミニウムイソプロピレート、アルミニウムセカンダリーブチレートなどのアルコレートアルミニウム化合物、アルミニウムアルキルアセテート・ジイソプロピレート、アルミニウムビスエチルアセトアセテート・モノアセチルアセトネート等のアルミニウムキレート化合物、ネオデカン酸ビスマス(III)、2-エチルヘキサン酸ビスマス(III)、クエン酸ビスマス(III)、オクチル酸ビスマス等の有機金属化合物;ホスファゼン含有化合物、3-アミノプロピルトリエトキシシラン、N-β(アミノエチル)γ-アミノプロピルトリメトキシシラン等のアミノアルキル基置換アルコキシシラン;ヘキシルアミン、リン酸ドデシルアミン等のアミン化合物又はその塩;ベンジルトリエチルアンモニウムアセテート等の第4級アンモニウム塩;酢酸カリウム、酢酸ナトリウム、シュウ酸リチウム等のアルカリ金属の低級脂肪酸塩;ジメチルヒドロキシルアミン、ジエチルヒドロキシルアミン等のジアルキルヒドロキシルアミン;テトラメチルグアニジルプロピルトリメトキシシラン、テトラメチルグアニジルプロピルメチルジメトキシシラン、テトラメチルグアニジルプロピルトリス(トリメチルシロキシ)シラン等のグアニジル基を含有するシラン及びシロキサン等が例示されるが、(C)成分はこれらに限定されない。また、(C)成分は1種でも2種以上混合して使用してもよい。
-(D)成分-
(D)成分である加水分解性シラン及び/又はその部分加水分解縮合物は架橋剤として作用するものであり、このうち加水分解性シランとしては、例えば、テトラアルコキシシラン類や、アルキルトリアルコキシシラン、アルキルトリ(アルコキシ置換アルコキシ)シラン、アルキルトリアルケニロキシシランなどの、通常、3官能性又は4官能性のオルガノキシシラン類等を挙げることができる。
具体例としては、例えば、エチルシリケート、プロピルシリケートや、テトラエトキシシラン、テトラプロポキシシラン、メチルトリメトキシシラン、メチルトリエトキシシラン、エチルトリメトキシシラン、エチルトリエトキシシラン、メチルトリス(メトキシエトキシ)シラン、エチルトリス(メトキシエトキシ)シラン、メチルトリプロペノキシシラン、エチルトリプロペノキシシラン等及びこれらの部分加水分解縮合物が挙げられる。これらは1種単独でも2種以上を組み合わせても使用することができる。
また、(A)成分と(D)成分を予め混合したオルガノポリシロキサン組成物IIIと、(B)成分と(C)成分を予め混合したオルガノポリシロキサン組成物IVとの2液とすることもできるが、オルガノポリシロキサン組成物IVは長期保存した場合に増粘する場合があるため、上記組成物I、IIの2液とすることが好ましい。
ここで(A)成分と(B)成分がわかれてさえいれば、他の成分は任意に添加してもよい場合がある。
なお、更に、下記(E)成分、(F)成分、(G)成分から選ばれる1種又は2種以上を、オルガノシロキサン組成物Iからオルガノシロキサン組成物IVから選ばれる1種又は2種以上の組成物に任意に配合することができる。
(E)成分は充填剤(無機質充填剤及び/又は有機樹脂製充填剤)であり、この組成物から形成される硬化物に十分な機械的強度を与えるために使用される。この充填剤としては公知のものを使用することができ、例えば微粉末シリカ、煙霧質シリカ、沈降性シリカ、これらのシリカ表面を有機ケイ素化合物で疎水化処理したシリカ、ガラスビーズ、ガラスバルーン、透明樹脂ビーズ、シリカエアロゲル、珪藻土、酸化鉄、酸化亜鉛、酸化チタン、煙霧状金属酸化物などの金属酸化物、湿式シリカあるいはこれらの表面をシラン処理したもの、石英粉末、カーボンブラック、タルク、ゼオライト及びベントナイト等の補強剤、アスベスト、ガラス繊維、炭素繊維、炭酸カルシウム、炭酸マグネシウム、炭酸亜鉛などの金属炭酸塩、アスベスト、ガラスウール、微粉マイカ、溶融シリカ粉末、ポリスチレン、ポリ塩化ビニル、ポリプロピレンなどの合成樹脂粉末等が使用される。これらの充填剤のうち、シリカ、炭酸カルシウム、ゼオライトなどが好ましく、特に表面を疎水化処理した煙霧質シリカ、炭酸カルシウムが好ましい。
(F)成分は接着促進剤であり、この組成物から形成される硬化物に十分な接着性を与えるために使用される。接着促進剤(例えば、官能性基含有一価炭化水素基を有するアルコキシシラン(いわゆるカーボンファンクショナルシラン)等のシランカップリング剤など)としては公知のものが好適に使用され、ビニルシランカップリング剤、(メタ)アクリルシランカップリング剤、エポキシシランカップリング剤、アミノシランシランカップリング剤、メルカプトシランカップリング剤などが例示され、具体的には、ビニルトリメトキシシラン、ビニルトリエトキシシラン、ビニルトリプロペノキシシラン、ビニルトリス(β-メトキシエトキシ)シラン等のアルケニルトリオルガノキシシラン類、γ-メタクリロキシプロピルトリメトキシシラン、β-(3,4-エポキシシクロヘキシル)エチルトリメトキシシラン、γ-グリシドキシプロピルトリメトキシシラン、γ-グリシドキシプロピルメチルジエトキシシラン、N-β-(アミノエチル)γ-アミノプロピルトリメトキシシラン、γ-アミノプロピルトリエトキシシラン、3-2-(アミノエチルアミノ)プロピルトリメトキシシラン、γ-メルカプトプロピルトリメトキシシラン、イソシアネートシラン等が例示される。
特にγ-アミノプロピルトリエトキシシラン、3-2-(アミノエチルアミノ)プロピルトリメトキシシラン等のアミノシラン類、γ-グリシドキシプロピルトリメトキシシラン、β-(3,4-エポキシシクロヘキシル)エチルトリメトキシシラン等のエポキシシラン類、イソシアネートシラン等が好ましい。
(G)成分のオルガノポリシロキサンは、下記一般式(3)で示される、分子中に、(A)成分、(B)成分の様な、加水分解縮合・架橋(硬化)反応に関与し得る官能性基を含有しない、いわゆる無官能性の直鎖状ジオルガノポリシロキサン(シリコーンオイル成分)であり、必要に応じて、本発明組成物の希釈剤として作用するものである。
上記式(3)中、R2の置換又は非置換の一価炭化水素基としては、メチル基、エチル基、プロピル基、イソプロピル基、ブチル基、イソブチル基、tert-ブチル基、ペンチル基、ヘキシル基、ヘプチル基、オクチル基、2-エチルヘキシル基、ノニル基、デシル基、オクタデシル基等のアルキル基;シクロペンチル基、シクロヘキシル基等のシクロアルキル基;ビニル基、アリル基、ブテニル基、ペンテニル基、ヘキセニル基等のアルケニル基;フェニル基、トリル基、キシリル基、α-,β-ナフチル基等のアリール基;ベンジル基、2-フェニルエチル基、3-フェニルプロピル基等のアラルキル基;また、これらの基の水素原子の一部又は全部が、F、Cl、Br等のハロゲン原子やシアノ基等で置換された基、例えば、3-クロロプロピル基、3,3,3-トリフルオロプロピル基、2-シアノエチル基等を例示することができる。これらの中でも、メチル基、エチル基が好ましく、入手の容易さ、生産性、コストの面からメチル基が特に好ましい。
また、本発明の室温硬化性オルガノポリシロキサン組成物には、更に、任意の添加剤として、顔料、染料、老化防止剤、酸化防止剤、帯電防止剤、酸化アンチモン、塩化パラフィン等の難燃剤など公知の添加剤を配合することができる。更に、チクソ性向上剤としてのポリエーテル、防かび剤、抗菌剤、を配合することもできる。
また、前記室温硬化性オルガノポリシロキサン組成物は、室温で放置することにより硬化するが、その成形方法、硬化条件などは、組成物の種類に応じた公知の方法、条件を採用することができる。
実施例で用いた両末端がトリメトキシシリル-エチレン基で封鎖されたジメチルポリシロキサン化合物の合成方法は、以下の通りである。
機械攪拌機、温度計及び滴下ロートを備えた5000mLの四つ口セパラブルフラスコに、オクタメチルシクロテトラシロキサン3050g、1,3-ジエチニル-1,1,3,3-テトラメチルジシロキサン32g、濃硫酸(H2SO4)154gを入れ、室温(23℃)で3時間以上撹拌した。その後、水(H2O)66gを加え、1時間以上撹拌し、トルエン500mLを加え、廃酸分離後にトルエン溶液を中性になるまで水洗洗浄した。トルエンと低分子シロキサンを150℃/8mmHgで、減圧下ストリップして下記に示す粘度935mPa・sのポリマーAを得た。
機械攪拌機、温度計及び滴下ロートを備えた5000mLの四つ口セパラブルフラスコに、ポリマーA1000g、トリメトキシシラン6.4g、塩化白金酸(H2PtCl6・6H2O)0.5gを入れ、70℃で3時間撹拌した。その後、120℃/20mmHgで減圧下ストリップして下記に示す粘度970mPa・sのポリマーBを得た。
第1成分として、100質量部のポリマーBに、ジオクチル錫ジラウレート0.5部を減圧下で均一になるまで混合して組成物Iを得た。第2成分として、分子鎖両末端水酸基封鎖の直鎖状ジメチルポリシロキサン(25℃の粘度5000mPa・s)100質量部を、組成物IIとした。組成物Iと組成物IIを湿気遮断下で混合し、室温硬化性オルガノポリシロキサン組成物1を調製した。
第1成分として、100質量部のポリマーBに、テトラメチルグアニジルプロピルトリメトキシシラン0.25部を減圧下で均一になるまで混合して組成物Iを得た。第2成分として、分子鎖両末端水酸基封鎖の直鎖状ジメチルポリシロキサン(25℃の粘度5000mPa・s)100質量部を、組成物IIとした。組成物Iと組成物IIを湿気遮断下で混合し、室温硬化性オルガノポリシロキサン組成物2を調製した。
第1成分として、100質量部のポリマーBに、ネオデカン酸ビスマス(III)0.51部を減圧下で均一になるまで混合して組成物Iを得た。第2成分として、分子鎖両末端水酸基封鎖の直鎖状ジメチルポリシロキサン(25℃の粘度5000mPa・s)100質量部を、組成物IIとした。組成物Iと組成物IIを湿気遮断下で混合し、室温硬化性オルガノポリシロキサン組成物3を調製した。
実施例1~3において、第1成分の分子鎖両末端がトリメトキシシリル-エチレン基で封鎖された直鎖状ジメチルポリシロキサン(ポリマーB)100部の代わりに分子鎖末端がトリメトキシシリル-エタン残基で封鎖された直鎖状ジメチルポリシロキサン(粘度1000mPa・s)100部を用いた以外は同様に組成物を調製した。
実施例1~3において、第一成分の分子鎖両末端がトリメトキシシリル-エチレン基で封鎖された直鎖状ジメチルポリシロキサン(ポリマーB)100部の代わりに分子鎖末端がトリメトキシシロキシ基で封鎖された直鎖状ジメチルポリシロキサン(粘度1000mPa・s)100部を用いた以外は同様に組成物を調製した。
また、実施例1~3及び比較例1~6で調製された調製直後の各組成物を厚さ2mmのシート状に押し出し、23±2℃,50±5%RH(相対湿度)の空気に曝し、次いで、該シートを同じ雰囲気下に3日間放置して得た硬化物の物性(初期物性)を、JIS K-6249に準拠して測定した。なお、硬さは、JIS K-6249のデュロメーターA硬度計を用いて測定した。
更に、この硬化物を85℃,85%RHの恒温恒湿器に7日間保管したものを同様に測定した。また、この硬化物を150℃のオーブンで10日間加熱したものを同様に測定した。また、実施例1~3及び比較例1~6で調製された調製直後の各組成物を密閉容器に入れて、70℃の温度で7日間放置したものから作った厚さ2mmのシートについても、23±2℃,50±5%RH(相対湿度)の空気中に3日間放置して得た硬化物に対して同様の測定を行った。
これらの結果を表1、表2、表3に示した。
第1成分として、ポリマーBを100質量部に、充填剤(表面をジメチルクロロシランで疎水化処理した煙霧質シリカ)を13部、粘度100mPa・sの分子鎖両末端がトリメチルシロキシ基で封鎖された直鎖状ジメチルポリシロキサン5部、テトラメチルグアニジルプロピルトリメトキシシラン1部を減圧保持下で均一になるまで混合して組成物Iを得た。第2成分として、分子鎖両末端水酸基封鎖の直鎖状ジメチルポリシロキサン(25℃の粘度5000mPa・s)100質量部とビニルトリメトキシシラン5部、3-アミノプロピルトリエトキシシラン0.8部、N-2-(アミノエチル)-3-アミノプロピルトリメトキシシラン0.8部を混合し、組成物IIとした。組成物Iと組成物IIを湿気遮断下で混合し、室温硬化性オルガノポリシロキサン組成物4を調製した。
実施例4において、ポリマーBの代わりに粘度1000mPa・sの分子鎖両末端がトリメトキシシリル-エタン基で封鎖された直鎖状ジメチルポリシロキサン100部を用いた以外は同様の手法で組成物7を調製した。
実施例4において、ポリマーBの代わりに粘度1000mPa・sの分子鎖両末端がトリメトキシシロキシ基で封鎖された直鎖状ジメチルポリシロキサン100部を用いた以外は同様の手法で組成物8を調製した。
これらの結果を表4に示した。
Claims (9)
- (A)下記構造式(1)で表される基を少なくとも分子中に1つ有するアルコキシシリル-エチレン基末端オルガノポリシロキサン
(式中、R1は置換基を有してもよい炭素数1から20のアルキル基であり、該アルキル基のうち炭素数が3以上のものは環状であるシクロアルキル基であってもよい。R2は置換基を有してもよい炭素数1から20の炭化水素基である。aは1から3の整数であり、nは0から10の整数である。)
(B)下記一般式(2)で示されるオルガノポリシロキサン (A)成分100質量部に対して10~250質量部、
(式中、R2は置換基を有してもよい炭素数1から20の炭化水素基である。mはオルガノポリシロキサンの25℃における粘度を10~1,000,000mPa・sとする数である。) 及び
(C)硬化触媒 (A)成分100質量部に対して0.001~20質量部、
を含有することを特徴とする室温硬化性オルガノポリシロキサン組成物。 - 前記(A)成分の主鎖がジオルガノシロキサン単位の繰返しからなる直鎖状オルガノポリシロキサンであることを特徴とする請求項1記載の室温硬化性オルガノポリシロキサン組成物。
- (A)成分と(C)成分と、必要により(G)成分及び/又は(E)成分とを含有するオルガノポリシロキサン組成物Iと、(B)成分と必要により(D)成分及び/又は(E)成分とを含有するオルガノシロキサン組成物IIからなる2液型であることを特徴とする請求項4に記載の室温硬化性オルガノポリシロキサン組成物。
- 更に、(F)成分及び/又は(G)成分をオルガノシロキサン組成物I及び/又はオルガノシロキサン組成物IIに配合した請求項5に記載の室温硬化性オルガノポリシロキサン組成物。
- 請求項1~6の何れか1項に記載の室温硬化性オルガノポリシロキサン組成物を含有することを特徴とする、シール剤、コーティング剤又は接着剤。
- 請求項1~6の何れか1項に記載の室温硬化性オルガノポリシロキサン組成物の硬化物。
- 請求項8に記載の硬化物からなる成型物。
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KR102207422B1 (ko) | 2021-01-26 |
EP3085739A4 (en) | 2017-08-02 |
CN105829449A (zh) | 2016-08-03 |
US20170306099A1 (en) | 2017-10-26 |
US9850349B2 (en) | 2017-12-26 |
EP3085739A1 (en) | 2016-10-26 |
EP3085739B1 (en) | 2020-03-11 |
JPWO2015093139A1 (ja) | 2017-03-16 |
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KR20160099630A (ko) | 2016-08-22 |
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