JPH0953010A - Curable resin composition - Google Patents

Abstract

PROBLEM TO BE SOLVED: To obtain a cheap curable resin composition which can give a cured product having reduced surface tackiness even in the initial stage of curing without detriment to modulus and elongation at break by mixing an oxyalkylene polymer with a hydrocarbon compound and a silicon compound. SOLUTION: This curable resin composition is prepared by mixing 100 pts.wt. oxyalkylene polymer (A) having a main chain comprising repeating units each represented by formula I (wherein R<1> is a 1-14C bivalent alkylene), containing one or more reactive silicic groups each represented formula II wherein R<2> and R<3> are each a 1-20C alkyl, a 6-20C aryl, a 7-20C aralkyl or a triorganosiloxy group represented by the formula: (R<4> )3 SiO- [wherein R<4> is a 1-20C monovalent hydrocarbon groups]; X is a hydrolyzable group or hydroxyl; (a) is 0-2; and (b) is 0-3} and having a molecular weight of 500-50,000 with 0.1-150 pts.wt. paraffinic hydrocarbon (B) being an aliphatic hydrocarbon, 0.1-30 pts.wt. long- chain-hydrocarbon-group-containing silicon compound (C) being an 8-29C alkyl silicon compound and optionally 0.1-100 pts.wt. (in terms of the total of components B and D) plasticizer (D) and a silanol condensation catalyst.

Description

Detailed Description of the Invention

[0001]

FIELD OF THE INVENTION The present invention relates to a curable composition which is cured in the presence of moisture and has improved surface tackiness from the initial stage of curing.

[0002]

2. Description of the Related Art A polymer having a reactive silicon group is crosslinked and cured in the presence of moisture.
A curable composition using, for example, a polyoxypropylene main chain skeleton in the polymer has a property of being a liquid at room temperature and becoming a rubber elastic body upon curing, and is widely used as a sealant for construction and the like. ing. However, depending on the compounding composition and the curing conditions, this curable composition has been a problem because tack (stickiness) remains on the surface of the cured product and dust or the like adheres to it to impair the appearance.

Therefore, as a method for improving this drawback,
For example, JP-A-55-21453 proposes a method of adding an organic silicon polymer to the polymer. However, this method has a problem that although the tack is improved, the modulus, strength at break and elongation are lowered. Further, JP-A-55-36241 discloses a method of adding a photocurable substance, JP-A-1-149851 discloses a method of adding a liquid diene polymer, and JP-A-1-188557 discloses a long-chain carbonization. A method of adding a hydrogen group-containing silicon compound is disclosed. However, these methods not only make the curable composition expensive, but also do not provide sufficient tack at the relatively early stages of curing, and do not provide sufficient effects depending on the composition and curing conditions. There was a flaw.

[0004]

In order to solve the above problems, the present invention has investigated the effects of various additives, and as a result, by adding a hydrocarbon and a long chain hydrocarbon group-containing silicon compound to the organic polymer. It was based on the finding that the surface tack was extremely good even in the initial stage of curing without lowering the modulus and elongation at break. That is, the present invention provides (a) an oxyalkylene polymer containing at least one reactive silicon group in one molecule, (b) a hydrocarbon compound, and (c) a long chain hydrocarbon group-containing silicon compound. It relates to a curable composition to be contained.

[0005]

BEST MODE FOR CARRYING OUT THE INVENTION (a) contained in the composition of the present invention
The main chain skeleton of the oxyalkylene polymer containing at least one reactive silicon group in one molecule essentially has the repeating unit represented by the general formula (1).

—R ¹ —O— (1) (In the formula, R ¹ is a divalent organic group and has 1 to 14 carbon atoms.
The straight-chain or branched alkylene group of is preferable) As specific examples of the repeating unit represented by the general formula (1),
_{-CH 2 O -, - CH 2} CH 2 O -, - CH 2 CH (C
_{H 3) O -, - CH} 2 CH (C 2 H 5) O -, - CH 2
_{C (CH 3) 2 O -} , - CH 2 CH 2 CH 2 CH 2 O-
And the like. The main chain skeleton of the oxyalkylene polymer may be composed of only one type of repeating unit or may be composed of two or more types of repeating units. In particular, when used as a sealant or the like, it is preferably composed of a polymer containing propylene oxide as a main component.

Examples of the reactive silicon group contained in the component (a) of the composition of the present invention include groups represented by the following general formula (2). -[-Si (R ² _2-a ) (X _a ) -O-] _m Si (R ³ _3-b ) -X _b (2) In the formula, each of R ² and R ³ has 1 to 1 carbon atoms. 20 alkyl group, C6-20 aryl group, C7-20
Aralkyl group or (R ⁴ ) ₃ SiO— [R ⁴ is a monovalent hydrocarbon group having 1 to 20 carbon atoms, and three R ⁴ may be the same or different] When a triorganosiloxy group is shown and two or more R ² and R ³ are present, they may be the same or different. X represents a hydrolyzable group or a hydroxyl group, and when two or more X are present, they may be the same or different. a is 0, 1 or 2,
b represents 0, 1, 2 or 3 respectively. the m general formula _{^{(3) -Si (R 2 2}} -a) (X a) -O- a need not be the same in (3). m is 0 or 1-1
Indicates an integer of 9. However, it is assumed that (a + Σb) ≧ 1 is satisfied.

The hydrolyzable group represented by X is not particularly limited and may be a conventionally known hydrolyzable group. Specific examples include a hydrogen atom, a halogen atom, an alkoxy group, an acyloxy group, a ketoximate group, an amino group, an amide group, an acid amide group, an aminooxy group, a mercapto group, and an alkenyloxy group. Among these, a hydrogen atom, an alkoxy group, an acyloxy group, a ketoximate group, an amino group, an amide group,
An aminooxy group, a mercapto group and an alkenyloxy group are preferable, and an alkoxy group is particularly preferable from the viewpoint of mild hydrolyzability and easy handling.

This hydrolyzable group or hydroxyl group can be bonded to one silicon atom in the range of 1 to 3 and (a + Σ
b) is preferably in the range of 1 to 5. When two or more hydrolyzable groups or hydroxyl groups are bonded to the reactive silicon group, they may be the same or different.

The number of silicon atoms forming the reactive silicon group is 1
The number may be two or more, but in the case of silicon atoms linked to a siloxane bond or the like, the number may be about 20.

Of these reactive silicon groups, the group represented by the following general formula (4) is preferable because it is easily available. _{^{-Si (-R 3 3-b)}} (X b) (4) In the formula, R ^3, X, b are the same as defined above.

Further, R ² and R ³ in the general formula (2) are
Specific examples include, for example, alkyl groups such as methyl group and ethyl group, cycloalkyl groups such as cyclohexyl group, aryl groups such as phenyl group, aralkyl groups such as benzyl group, R ⁴ is methyl group, phenyl group. Etc. (R ⁴ ) ₃ S
Examples thereof include a trimethylsiloxy group represented by iO-. Of these, a methyl group is particularly preferable.

The reactive silicon group can be introduced by a known method. For example, the following method can be used. (i) An oxyalkylene polymer having a functional group such as a hydroxyl group in the molecule is reacted with an organic compound having an active group and an unsaturated group which are reactive with this functional group to form an oxy group containing an unsaturated group. An alkylene polymer is obtained. Alternatively, an unsaturated group-containing oxyalkylene polymer is obtained by copolymerization with an unsaturated group-containing epoxy compound. Then, the obtained reaction product is treated with hydrosilane having a reactive silicon group to carry out hydrosilylation.

(Ii) A method of reacting an unsaturated group-containing oxyalkylene polymer obtained in the same manner as in the method (i) with a compound having a mercapto group and a reactive silicon group. (iii) A method of reacting an oxyalkylene polymer having a functional group such as a hydroxyl group, an epoxy group and an isocyanate group in the molecule with a compound having a functional group reactive with the functional group and a reactive silicon group.

Among these methods, the method (i) or
Among (iii), a method of reacting a polymer having a hydroxyl group at the terminal with a compound having an isocyanate group and a reactive silicon group is preferable.

The oxyalkylene polymer as the component (a) used in the present invention may be linear or branched, and its molecular weight is 500 to 50,000.
It is preferably about 0, more preferably 1,000 to 20,000. The number of reactive silicon groups contained in this polymer is preferably at least 1, preferably 1.1 to 5, in one molecule of the polymer. When the number of reactive silicon groups contained in the molecule is less than 1, the curability becomes insufficient, and when it is too large, the network structure becomes too dense and good mechanical properties are not exhibited.

Specific examples of the oxyalkylene polymer which is the component (a) of the present invention include, for example, JP-B-45-36319, JP-A-46-12154 and JP-A-50-156599.
54-6096 publication, 55-13767 publication, 55-13768 publication, 57-164123 publication, Japanese Examined Patent Publication 3-2450 publication, U.S. Pat.No. 3,632,557 specification, 4,345,053 specification, and the same.
Those disclosed in the specifications of 4,366,307 and 4,960,844, and the disclosures of JP-A-61-197631 and 61-215.
No. 622, No. 61-215623, No. 61-218632, the number average molecular weight of 6,000 or more, M _w /
M _m is the molecular weight distribution can be exemplified a narrow oxyalkylene polymer with a high molecular weight of 1.6 or less, but it is not particularly limited thereto.

The oxyalkylene polymer containing a reactive silicon group may be used alone or in combination of two or more kinds. Further, an oxyalkylene polymer obtained by blending a vinyl polymer having a reactive silicon group can also be used.

A method for producing an oxyalkylene polymer blended with a vinyl polymer having a reactive silicon group is described in JP-A-59-122541, JP-A-63-112642 and JP-A-6-17.
It is disclosed in Japanese Patent No. 2631. Specifically, an acrylic acid ester monomer unit having a reactive silicon group and a molecular chain substantially having an alkyl group having 1 to 8 carbon atoms represented by the following general formula (5) and / or methallylacrylic acid An ester monomer unit and 10 carbon atoms represented by the following general formula (6)
It is produced by blending an oxyalkylene polymer containing a reactive silicon group with the above-mentioned copolymer composed of an acrylic acid ester monomer unit and / or a methallylacrylic acid ester monomer unit having an alkyl group.

General formula (5): —CH ₂ —C (R ⁶ ) (COOR ⁵ ) — (5) In the formula, R ⁵ is an alkyl group having 1 to 8 carbon atoms, and R ⁶ is a hydrogen atom or a methyl group. Show. Formula _{(6) -CH 2 -C (R} 6) (COOR 7) - in (6), R ⁶ is as defined above, R ⁷ represents an alkyl group having 10 or more carbon atoms.

As R ^{5 in the} general formula (5), for example, methyl group, ethyl group, propyl group, n-butyl group, t-butyl group, 2-ethylhexyl group and the like having 1 to 8 carbon atoms, preferably 1 -4, more preferably 1-2 alkyl groups. The alkyl group of R ⁵ may be used alone or in combination of two or more.

Examples of R ^{7 in the} general formula (6) include lauryl group, tridecyl group, cetyl group, stearyl group,
An alkyl group having 22 carbon atoms, a long-chain alkyl group having 10 or more carbon atoms, usually 10 to 30, and preferably 10 to 20, such as behenyl group, can be mentioned. The alkyl group of R ⁷ is
Similar to the case of R ⁵ , they may be used alone or as a mixture of two or more kinds.

The molecular chain of this vinyl-based copolymer consists essentially of the monomer units of the formulas (5) and (6), but the term “substantially” as used herein means that it exists in the copolymer. Means that the total of the monomer units of the formulas (5) and (6) is more than 50% by weight. The total of the monomer units of formula (5) and formula (6) is preferably 70% by weight or more.

The abundance ratio of the monomer unit of the formula (5) to the monomer unit of the formula (6) is 95: 5 to 40: 6 by weight.
0 is preferable, and 90 to 10:60:40 is more preferable. Examples of the monomer unit other than the formula (5) and the formula (6) which may be contained in the copolymer include acrylic acid such as acrylic acid and methacrylic acid, acrylamide, methacrylamide, and N-methylolacrylamide. , Amide groups such as N-methylol methacrylamide, epoxy groups such as glycidyl acrylate and glycidyl methacrylate,
Amino group-containing monomers such as diethylaminoethyl acrylate, diethylaminoethyl methacrylate, and aminoethyl vinyl ether, other acrylonitrile, styrene, α-methylstyrene, alkyl vinyl ether,
Examples thereof include monomer units derived from vinyl chloride, vinyl acetate, vinyl propionate, ethylene and the like.

This copolymer has a number average molecular weight of 500 to
100,000 is preferable from the viewpoint of easy handling. Reactive silicon group The copolymer has the general formula (7) - [- Si ( R 8 2-a) (X a) -O-] n Si (R 8 3-b) -X b (7 (In the formula, R ⁸ represents a substituted or unsubstituted organic group having 1 to 20 carbon atoms or a triorganosiloxy group, X represents a hydroxyl group or a different or the same type of hydrolyzable group, a
Is an integer of 0, 1 or 2, and b is an integer of 0, 1, 2 or 3 and satisfies (a + Σb) ≧ 1.
n represents 0 or an integer of 1 to 19. ). A reactive silicon functional group which is preferable from the viewpoint of economical efficiency is —Si (R ⁸ _3-c ) —X _c (8) (wherein R ⁸ and X are the same as above. C is 1, 2, or Three
Integer. ) Is a group represented by.

The number of reactive silicon groups in this copolymer is one or more on average from the viewpoint of obtaining sufficient curability, and further,
1.1 or more, particularly 1.5 or more are preferable, and the number average molecular weight per apparently reactive silicon group is 300 to
It is preferably present so as to be 4,000.

Specific examples of the hydrolyzable group in the formula (7) include a halogen atom, a hydrogen atom, an alkoxy group, an acyloxy group, a ketoximate group, an amino group, an amide group,
Examples thereof include aminooxy group, mercapto group, alkenyloxy group and the like. Among these, alkoxy groups such as methoxy group and ethoxy group are preferable from the viewpoint of mild hydrolyzability.

Specific examples of R ⁸ in the formula (7) include, for example, alkyl groups such as methyl group and ethyl group, cycloalkyl groups such as cyclohexyl group, aryl groups such as phenyl group, benzyl group and the like. And the aralkyl group. Further, R ⁸ may be a trimethylsiloxy group represented by (R ⁹ ) ₃ SiO— (R ⁹ represents a substituted or unsubstituted organic group having 1 to 20 carbon atoms or a triorganosiloxy group). Of these, a methyl group is particularly preferable.

Further, as a method for producing an oxyalkylene polymer prepared by blending a vinyl polymer having a reactive silicon functional group, in addition, in the presence of an oxyalkylene polymer having a reactive silicon group ( It can be used for those who polymerize a (meth) acrylic acid ester-based monomer. This manufacturing method is described in JP-A-59-78223, JP-A-59-168014, and JP-A-60-2285.
No. 16, 60-228517, etc.
These are not limited.

In addition to the oxyalkylene polymer containing at least one reactive silicon group in one molecule of the component (a), another polymer having a reactive silicon group such as polydimethylsiloxane is added. You may.

As the hydrocarbon-based compound which is the component (b) of the composition of the present invention, generally known compounds can be used, and in particular, aliphatic hydrocarbons such as paraffin-based, olefin-based, diolefin-based and polyolefin-based compounds can be used. , Acetylene-based, etc. Structurally, it may be linear or branched. Further, a polymer of an unsaturated group-containing hydrocarbon and a reaction product obtained by adding hydrogen to the polymer can also be used.
Paraffinic hydrocarbons are more preferable, and if paraffinic hydrocarbons having 6 or more carbon atoms, and further having 8 to 18 carbon atoms are used, a remarkable effect can be obtained. Those having a small carbon number volatilize at a high temperature, and those having a large carbon number become a solid at a low temperature, so that a sufficient effect cannot be obtained depending on the temperature conditions used. Specifically, n-octane,
2-ethylheptane, 3-methylheptane, n-nonane, 2-methyloctane, 3-methyloctane, n-decane, 2-methylnonane, 3-methylnonane, n-undecane, n-dodecane,
Examples include n-tridecane, n-tetradecane, 4,5-dipropyloctane, 3-methyltridecane, 6-methyltridecane, n-hexadecane, n-heptadecane, and n-octadecane, but are not limited thereto. Not a thing. Also,
As the hydrocarbon compound as the component (b), only one kind may be used, or a mixture of two or more kinds may be used.

The amount of the hydrocarbon compound as the component (b) used is preferably 0.1 to 150 parts by weight, more preferably 1 to 150 parts by weight, relative to 100 parts by weight of the oxyalkylene polymer as the component (a).
60 parts by weight is preferred. If the amount is 0.1 part by weight or less, the effect of improvement does not appear, and if it exceeds 150 parts by weight, the mechanical strength of the cured product becomes insufficient, which is not preferable.

The long chain hydrocarbon group in the long chain hydrocarbon group-containing silicon compound which is the component (c) of the composition of the present invention is
For example, a long-chain alkyl group, a long-chain alkenyl group, a cycloalkyl group or an aryl group having a long-chain alkyl group or a long-chain alkenyl group having a silicon-based group bonded to one end, and a silicon-based group bonded to both ends. A long-chain alkylene group or the like in which the number of carbon atoms in the hydrocarbon portion (not including the hydrocarbon forming a ring) that is continuous in a straight chain is 8 or more, preferably 8 to 20. That is.

Specific examples of the long-chain alkyl group include, for example, n-octyl group, decyl group, undecyl group, dodecyl group, tridecyl group, tetradecyl group, cetyl group, stearyl group, eicosyl group, long-chain alkenyl group. Specific examples of, for example, octenyl group, nonenyl group, decenyl group, dodecenyl group, tetradecenyl group, hexadecenyl group, octadecenyl group, eicosenyl group, octadecadienyl group, 9,12,15-octadecatrienyl group, 9,11,1
3- octadecatrienyl group, specific examples of the long-chain alkylene group, for _{example, - (CH 2) 11 -} , - (CH 2)
_{13 -, - (CH 2)} 15 -, - (CH 2) 19 -, - (CH
₂ ) _20-, etc.

The long-chain hydrocarbon group-containing silicon compound also contains a reactive silicon group. This reactive silicon group is the same group as the reactive silicon group contained in the above-mentioned oxyalkylene polymer, but from the viewpoint of economy and the like, a reactive silicon group having one silicon atom is preferable.

Specific examples of the long chain hydrocarbon group-containing silicon compound include, for example, CH ₃ (CH ₂ ) ₉ Si (O
CH ₃ ) ₃ , CH ₃ (CH ₂ ) ₁₇ Si (OCH ₃ ) ₃ ,
_{CH 3 (CH 2) 11 Si} (OC 2 H 5) 3, CH 3 (C
H ₂ ) ₁₇ Si (OC ₂ H ₅ ) ₃ , CH ₃ (CH ₂ ) ₉ S
_{i (CH 3) (OCH 3} ) 2, CH 3 (CH 2) 17 Si
(CH ₃ ) (OCH ₃ ) ₂ , (CH ₃ O) ₃ Si (CH
₂ ) ₁₀ Si (OCH ₃ ) ₃ , (CH ₃ O) ₂ (CH ₃ )
Examples thereof include Si (CH ₂ ) ₁₀ Si (CH ₃ ) (OCH ₃ ) _{2 and the} like, but are not limited thereto.

The amount of the long-chain hydrocarbon group-containing silicon compound used is 100 parts by weight of the oxyalkylene polymer.
The amount is 0.1 to 30 parts by weight, preferably 0.5 to 20 parts by weight. If the amount used is less than 0.1 parts by weight, no improvement effect will be exhibited, and if it exceeds 30 parts by weight, the cost will be high and the tensile properties will be impaired.

In the composition of the present invention, a plasticizer may be used if necessary, and in that case, the addition amount thereof depends on the amount of the hydrocarbon compound of the component (b) contained. Need to be adjusted. When these additives are used so that the total amount of the hydrocarbon and the plasticizer is in the range of 0.1 to 100 parts by weight with respect to 100 parts by weight of the oxyalkylene polymer, preferable results are obtained. If it exceeds 100 parts by weight, the amount of the liquid component increases and the improvement effect cannot be obtained.

Examples of the plasticizer include phthalic acid esters such as dioctyl phthalate, diisodecyl phthalate, dibutyl phthalate and butylbenzyl phthalate; epoxy plasticizers such as epoxidized soybean oil, epoxidized linseed oil and benzyl epoxystearate; Polyester plasticizers such as polyesters of dibasic acids and dihydric alcohols; polyethers such as polypropylene glycol and its derivatives; polystyrenes such as poly-α-methylstyrene and polystyrene; polybutadiene and butadiene-acrylonitrile copolymerization Plasticizers such as coalesce, polychloroprene, polyisoprene, polybutene, and chlorinated paraffins may be optionally used alone or in the form of a mixture of two or more kinds.

The curable composition of the present invention may contain a silanol condensation catalyst in order to accelerate the reaction of the reactive silicon group. Examples of such silanol condensation catalyst include titanic acid esters such as tetrabutyl titanate and tetrapropyl titanate, dibutyltin dilaurate,
Dibutyltin maleate, dibutyltin diacetate, tin octylate, tin naphthenate, reaction products of dibutyltin oxide and phthalate ester, organic tin compounds such as dibutyltin diacetylacetonate, aluminum trisacetylacetate Organic aluminum compounds such as sodium nitrate, aluminum trisethylacetoacetate, diisopropoxyaluminum ethylacetoacetate, bismuth-tris- (2-ethylhexoate), bismuth-tris-
Reaction products of bismuth salts such as (neodecanoate) and organic carboxylic acids, such as zirconium tetraacetylacetonate
Chelate compounds such as titanium tetraacetylacetonate, organic lead compounds such as lead octylate, organic vanadium compounds, butylamine, octylamine, dibutylamine, monoethanolamine, diethanolamine, triethanolamine, diethylenetriamine, triethylene Tetramine, oleylamine, cyclohexylamine, benzylamine, diethylaminopropylamine,
Xylylenediamine, triethylenediamine, guanidine, diphenylguanidine, 2,4,6-tris (dimethylaminomethyl) phenol, morpholine, N-methylmorpholine, 2-ethyl-4-methylimidazole, 1,8-diazabicyclo ( Amine compounds such as 5,4,0) -7-undecene (DBU) or salts thereof with carboxylic acids, low molecular weight polyamide resins obtained from excess polyamine and polybasic acid, excess polyamine and epoxy compound Examples of the reaction product with and the like include, but are not limited to, a commonly used condensation catalyst can be used. These silanol condensation catalysts may be used alone or in combination of two or more kinds. Among these silanol condensation catalysts, organometallic compounds or a combined system of organometallic compounds and an amine compound is preferable from the viewpoint of curability.

The amount of these silanol condensation catalysts used is
10 of oxyalkylene polymer having reactive silicon group
The amount is preferably about 0.01 to 20 parts by weight, more preferably about 0.1 to 10 parts by weight, based on 0 parts by weight. If the amount of the silanol condensation catalyst used is too small with respect to the oxyalkylene polymer, the curing rate becomes slow and the curing reaction becomes difficult to proceed sufficiently, which is not preferable. On the other hand, if the amount of the silanol condensation catalyst used is too large with respect to the oxyalkylene polymer, local heat generation or foaming occurs during curing,
It is not preferable because it becomes difficult to obtain a good cured product.

The curable composition of the present invention may further contain a dehydrating agent, a compatibilizing agent, an adhesion improving agent, a physical property adjusting agent, if necessary.
Storage stability improver, filler, anti-aging agent, ultraviolet absorber, metal deactivator, ozone deterioration inhibitor, light stabilizer, amine radical chain inhibitor, phosphorus peroxide decomposer, lubricant, pigment Various additives such as a foaming agent, a flame retardant, and an antistatic agent can also be added as appropriate.

For example, when a filler is used as an additive, wood powder, walnut shell powder, chaff powder, pulp, cotton chips, mica, graphite, diatomaceous earth, clay, kaolin, clay, talc, fumed silica, Precipitable silica, silicic acid anhydride, quartz powder, glass beads, calcium carbonate, magnesium carbonate, titanium oxide, aluminum powder, zinc powder, asbestos, glass fiber, carbon fiber and the like can be used. These fillers may be used alone,
Two or more kinds may be used in combination.

A curable resin composition containing the oxyalkylene polymer as the component (a), the hydrocarbon compound as the component (b) and the long chain hydrocarbon group-containing silicon compound as the component (c) of the present invention is prepared. The method is not particularly limited, but specific examples include a method of simply adding a hydrocarbon compound and a long chain hydrocarbon group-containing silicon compound to an oxyalkylene polymer. In this case, if necessary, heating and stirring conditions may be appropriately adjusted to uniformly disperse and dissolve. However, it is not necessary to have a completely uniform and transparent state,
Even in the opaque state, the effect can be sufficiently obtained if dispersed. Further, a dispersibility improver may be used in combination, if necessary. In addition, a method of dissolving each component by using a mixer, a roll, a kneader or the like and mixing them may be adopted.

The composition thus obtained is
It can be applied not only to a two-pack type but also to a one-pack type curable composition.
In the latter case, the composition of the present invention is obtained by adjusting the composition of the present invention in a substantially water-free state, and it can withstand long-term storage if stored in a closed state, and quickly starts curing from the surface when exposed to the atmosphere. To do.

The composition of the present invention is useful as an elastic sealing material in the fields of construction, civil engineering, industrial use and the like, and can be used as a paint, an adhesive, an injecting agent, and a coating material.

[0047]

EXAMPLES Next, the curable composition of the present invention will be described in detail with reference to examples, but the present invention is not limited to these examples. Examples 1-8, Comparative Examples 1 to 3 per molecule average of two methyldimethoxysilyl group _{-Si (CH 3) (OCH 3} ) 100 parts by weight of the average molecular weight of 8,000 propylene oxide polymers containing ₂ , 120 parts by weight of surface-treated colloidal calcium carbonate (average particle size 0.08 μm), titanium oxide 2
0 parts by weight, hydrogenated castor oil 2 parts by weight, dibutyltin diacetylacetonate 1 part by weight, and further the hydrocarbons shown in Table 1,
KBM3103C [Shin-Etsu Silicone, CH ₃ (CH
₂ ) ₉ Si (OCH ₃ ) ₃ ] or TSL8185 [manufactured by Toshiba Silicone Co., Ltd., CH ₃ (CH ₂ ) ₁₇ Si (OCH
₃ ) ₃ ] and DIDP (diisodecyl phthalate) in the amounts shown in Table 1 were sufficiently kneaded in a substantially water-free state to obtain a curable resin composition.

In Table 1, undecane is a product of Wako Pure Chemical Industries, and YH-NP is Nikko Petrochemical normal paraffin (n-dodecane 18%, n-tridecane 59%, n-
Tetradecane 19%, n-heptadecane 4%), S
H-NP is a Nikko petrochemical normal paraffin (n-tetradecane 55%, n-heptadecane 37%, n-hexadecane 8%).

The composition thus obtained was spread to a thickness of 3 mm and cured at 23 ° C. and 55% RH,
The tack remaining on the surface was evaluated by touch with a finger. The results are shown in Table 1, and are also shown in the case of the comparative example in which the hydrocarbon and the long-chain hydrocarbon group-containing silicon compound are not used in combination.

[0050]

[Table 1]

From the results shown in Table 1, it is understood that the addition of the hydrocarbon and the long-chain hydrocarbon group-containing silicon compound makes it possible to obtain a cured product with improved tack remaining on the surface one day after curing.

Claims (4)

[Claims] 1. An (a) oxyalkylene polymer containing at least one reactive silicon group in one molecule, (b) a hydrocarbon compound, and (c) a long chain hydrocarbon group-containing silicon compound. A curable composition containing the same. 2. The curable composition according to claim 1, wherein the hydrocarbon compound is an aliphatic hydrocarbon. 3. The curable composition according to claim 1, wherein the hydrocarbon compound is a paraffin hydrocarbon. 4. The curable composition according to claim 1, wherein the long chain hydrocarbon group-containing silicon compound is an alkyl group-containing silicon compound having 8 to 20 carbon atoms.