JP2005082734A - Room temperature-curable polyorganosiloxane composition - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To obtain a room temperature-curable organopolysiloxane composition exhibiting excellent physical properties after cured and having improved adhesion properties, and showing excellent releasability from a bond area with a substrate. <P>SOLUTION: This room temperature-curable polyorganosiloxane composition is obtained by combiningly using a combination of a polyorganosiloxane having the both ends blocked with a trialkoxysilyl group and another polyorganosiloxane having the both ends blocked with a dialkoxymonoorganosilyl group as base polymers, and further combingly using a silicone oil having no reactivity with the above polymers, and a two functional alkoxysilane crosslinking agent. <P>COPYRIGHT: (C)2005,JPO&NCIPI

Description

  The present invention relates to a composition that is cured at room temperature to become a silicone elastomer, and more specifically, room temperature curability that has excellent physical properties after curing, improved adhesion, and excellent releasability from the adhesion surface to the substrate. A polyorganosiloxane composition is provided.

  Among the polyorganosiloxane compositions that cure at room temperature to produce rubbery elastic bodies, those that cause a curing reaction when in contact with moisture in the air are the main body (base polymer) or crosslinked immediately before use. There is no need to weigh agents or catalysts or mix them, and there are no mistakes in blending, and it is excellent in adhesiveness, so elastic adhesives and coatings in the electric / electronic industry etc. It is widely used as a material and as a sealing material for construction. Such a composition is generally prepared by blending a silanol group-terminated polyorganosiloxane whose molecular terminal is blocked with a hydroxyl group with a crosslinking agent having more than two hydrolyzable groups in the molecule. Depending on the type, carboxylic acids such as acetic acid, organic amines, amides, organic hydroxylamines, oxime compounds, alcohols, acetone, etc. are released upon curing.

  Of these, the dealcohol-free type is not only cheaply available as an alkoxysilane as a cross-linking agent, but also has the advantage of being easy to volatilize because the release material is an alcohol such as methanol or ethanol, and has no odor problems, metal corrosion Therefore, it is widely used as a coating material for electrical and electronic equipment.

  However, the dealcohol-free type is slow to cure and has poor storage stability because the alcohol generated by hydrolysis of the crosslinking agent by the trace amount of water present in the system during storage cleaves the base polymer. There were difficulties and there was a need to overcome it. In order to solve this problem, in Patent Documents 1 and 2, a base polymer is a polyorganosiloxane having both ends blocked with dialkoxymonoorganosilyl groups or a polyorganosiloxane having both ends blocked with trialkoxysilyl groups. As a filler, the surface treated silica as a filler, the alkoxysilane as a crosslinking agent, and a titanium chelate catalyst are selectively combined to improve storage stability and curing rate (surface film formation rate).

  However, according to the inventor's follow-up test, according to the techniques of the above-mentioned Patent Documents 1 and 2, a composition excellent in storage stability and curing speed can be obtained to some extent, but the adhesiveness is not yet satisfactory. It was.

  On the other hand, in the field of electrode coating for LCDs, etc., after curing the curable polyorganosiloxane composition, it may be necessary to remove it from the adhesive surface with the substrate and peel it off for repair, etc. At this time, it is required that the cured product does not remain on the surface of the base material and the interface is peeled off.

As a curable polyorganosiloxane composition having such characteristics, Patent Document 3 proposes a selective combination of a polyorganosiloxane blocked at both ends with trialkoxysilyl groups, a bifunctional alkoxysilane, and a titanium chelate catalyst. However, according to the additional test of the present inventor, the interface peeling from the base material was possible, but the adhesion to the base material was low and it was not satisfactory as a sealing material.
Japanese Examined Patent Publication No. 5-72424 Japanese Patent Publication No. 5-88866 Japanese Unexamined Patent Publication No. Hei 4-2933962

  The object of the present invention is to solve the above-mentioned drawbacks of the prior art, to improve the physical properties after curing, to improve the adhesion, and to improve the peelability from the adhesion surface with the substrate, and a room temperature curable organopolysiloxane composition. Is to provide.

  The inventors of the present invention have studied to obtain a room temperature curable organopolysiloxane composition that can achieve the above-mentioned object. As a result, the base polymer is a polyorganosiloxane having both ends blocked with trialkoxysilyl groups and both ends are dialkoxy. It is found that it is extremely effective to use a polyorganosiloxane blocked with a monoorganosilyl group in combination with a non-reactive silicone oil and a bifunctional alkoxysilane crosslinking agent, thereby completing the present invention. It reached.

That is, the present invention
(A) 5 to 95% by weight of polyorganosiloxane having a viscosity at 25 ° C. of 0.1 to 1000 Pa · s and both ends blocked with trialkoxysilyl groups
(B) Polyorganosiloxane having a viscosity at 25 ° C. of 0.1 to 1000 Pa · s and both ends blocked with dialkoxymonoorganosilyl groups 95 to 5% by weight
For 100 parts by weight of polyorganosiloxane consisting of
(C) 1-50 parts by weight of a polyorganosiloxane containing no silanol group, trialkoxy group and dialkoxy group in the molecule and having a viscosity at 25 ° C. lower than the viscosity of the component (A) and / or the component (B),
(D) 1 to 50 parts by weight of silica powder having a specific surface area of 50 m ² / g or more,
(E) 0.5 to 15 parts by weight of a bifunctional alkoxysilane or a partially hydrolyzed condensate thereof,
(F) A room temperature-curable polyorganosiloxane composition comprising 0.1 to 15 parts by weight of a titanium chelate catalyst.

  In the present invention, a combination of terminal trifunctional and bifunctional polymers (component (A) and component (B)) develops appropriate rubber strength, silicone oil (C) having no reactivity with these, and bifunctional By blending the alkoxysilane cross-linking agent (D), high adhesiveness is exhibited, and further, excellent releasability is produced by a balance between these.

  Hereinafter, the present invention will be described in detail. The polyorganosiloxane of the components (A) and (B) used in the present invention is a base polymer of the composition, and (A) a polyorganosiloxane having both ends blocked with trialkoxysilyl groups and (B) The polyorganosiloxane having both ends blocked with dialkoxymonoorganosilyl groups, the component (A) is 5 to 95% by weight, the component (B) is 95 to 5% by weight, more preferably the component (A) is 10 to 90%. It is a blend of 90 to 10% by weight of component (B) with respect to% by weight. When the component (A) is less than 5% by weight, the interfacial peelability from the substrate is poor, and when it exceeds 95% by weight, the adhesion to the substrate is lowered. Methods for producing such polydiorganosiloxanes are well known, for example, a method in which a polydiorganosiloxane having hydrosilyl groups at both ends of the molecular chain and an alkenyltrialkoxysilane or alkenylalkyldialkoxysilane are subjected to an addition reaction; Addition reaction of polydiorganosiloxane having alkenylsilyl groups at both ends and trialkoxysilane or alkyldialkoxysilane; polydiorganosiloxane having hydroxysilyl groups at both ends of molecular chain and tetraalkoxysilane or alkyltrialkoxysilane Is exemplified by a method of subjecting the alcohol to a dealcohol condensation reaction.

  In the components (A) and (B), there is no particular limitation except for the terminal structure, and any ordinary polyorganosiloxane such as a straight chain may be used. As the substituent bonded to the silicon atom, an alkyl group, Monovalent hydrocarbon groups such as cycloalkyl groups, alkenyl groups, aryl groups and aralkyl groups, halogenated hydrocarbon groups such as chloromethyl groups and trifluoromethyl groups, and cyanoalkyl groups such as β-cyanoethyl groups and γ-cyanopropyl groups Groups.

  The viscosity of the component (A) is preferably 0.1 to 1000 Pa · s, more preferably 0.2 to 100 Pa · s. If it is lower than 0.1 Pa · s, the rubber becomes brittle and the interfacial peelability becomes worse. On the other hand, if it is higher than 1000 Pa · s, the fluidity is deteriorated and the sealing property is deteriorated.

  The viscosity of the component (B) is preferably 0.1 to 1000 Pa · s, more preferably 0.2 to 100 Pa · s. If it is lower than 0.1 Pa · s, the rubber becomes brittle and the interfacial peelability deteriorates. On the other hand, if it is higher than 1000 Pa · s, the fluidity is deteriorated and the sealing property is deteriorated.

  As the component (C) used in the present invention, the polyorganosiloxane increases the adhesion to the substrate. It does not contain a silanol group, trialkoxy group or dialkoxy group in the molecule. The terminal is preferably a triorganosilyl group, and the side chain is preferably the same type as the components (A) and (B). The viscosity of component (C) at 25 ° C. must be at least lower than the viscosity of either component (A) or component (B), preferably from the viscosity of both component (A) and component (B). It is low. This is because if the viscosity of the component (C) is higher than the viscosity of the component (A) and the component (B), the cured product bleeds and adhesion decreases. Specifically, the viscosity of the component (C) is preferably 0.02 to 10 Pa · s.

  The component (C) is used in an amount of 1 to 50 parts by weight based on 100 parts by weight of the total of the components (A) and (B). If the blending amount is less than 1 part by weight, sufficient adhesion cannot be obtained, and if it exceeds 50 parts by weight, the rubber strength is lowered and the interfacial peelability is lowered. More preferably, it is 3 to 30 parts by weight.

The filler of the component (D) used in the present invention is a silica powder having a specific surface area of 50 m ² / g or more, and fumed silica, calcined silica, or these surfaces are treated with organochlorosilanes, polyorganosiloxanes, organosilazanes. And the like which have been surface-treated with a conventionally known treating agent such as the above. The specific surface area mentioned here is based on the BET method. Those treated with organosilazanes are preferred. More preferred is fumed silica treated with organosilazanes to a carbon content of 2% or more.

  The component (D) is used in an amount of 1 to 50 parts by weight with respect to 100 parts by weight as the total of the components (A) and (B).

  Next, the component (E) used in the present invention is a bifunctional alkoxysilane or a partial hydrolysis condensate thereof, and acts as a crosslinking agent.

  Specific examples of the component (E) include bifunctional alkoxysilanes such as dimethyldimethoxysilane, phenylmethyldimethoxysilane, diphenyldimethoxysilane, vinylmethyldimethoxysilane, dimethyldiethoxysilane, methylpropyldimethoxysilane, and methylvinyldiethoxysilane. And a partial hydrolysis-condensation product thereof. If trifunctional or monofunctional alkoxysilanes are used as the crosslinking agent, sufficient adhesion and interfacial peelability cannot be obtained.

  The component (E) is used in an amount of about 0.5 to 15 parts by weight with respect to a total of 100 parts by weight of the components (A) and (B). If the amount is less than 0.5 part by weight, the storage stability is poor and sufficient adhesion cannot be obtained. If the amount exceeds 15 parts by weight, the rubber strength is lowered and the interfacial peelability is lowered.

  As the titanium chelate catalyst of the component (F) used in the present invention, diisopropoxy bis (ethyl acetoacetate) titanium, diisopropoxy bis (methyl acetoacetate) titanium, diisopropoxy bis (acetoacetone) titanium, dibutoxy bis ( Well-known various titanium chelate compounds, such as an ethyl acetoacetate titanium and dimethoxybis (ethyl acetoacetate) titanium, are mentioned.

  The component (F) is used in an amount of about 0.1 to 15 parts by weight with respect to a total of 100 parts by weight of the components (A) and (B).

  The composition of the present invention comprises the above components (A) to (F). In addition to the above components, inorganic fillers such as quartz fine powder, carbon black and calcium carbonate, and those Hydrophobized, thixotropy imparting agent, viscosity modifier, fluidity modifier, pigment, heat resistance agent, flame retardant, organic solvent, antifungal agent, antibacterial agent, ultraviolet absorber, heat resistance improver, flame retardant Addition of various additives such as an agent and an adhesion improver may be performed as long as the object of the present invention is not impaired.

Hereinafter, the present invention will be specifically described with reference to examples. However, the present invention is not limited to the following examples. In the examples, “part” means part by weight.
Example 1
Polymer (A) (polyorganosiloxane having a hydroxysilyl group at both ends of the molecular chain and tetramethoxysilane subjected to a dealcoholization condensation reaction and having both ends blocked with a trimethoxysilyl group (viscosity of 3 Pa at 25 ° C.・ S)) 50 parts, polymer (B) (polydimethylsiloxane having hydroxysilyl groups at both ends of the molecular chain and methyltrimethoxysilane subjected to dealcoholization condensation reaction, both ends blocked with methyldimethoxysilyl groups 50 parts of organosiloxane (viscosity of 3 Pa · s at 25 ° C), 10 parts of silicone oil (C) (dimethylsiloxane blocked at both ends with trimethylsilyl groups (viscosity of 0.1 Pa · s at 25 ° C)), by BET method dry silica (mosquitoes specific surface area surface-treated with hexamethyldisilazane at 170m ² / g Bon amount 3.0% Silica A) were blended 15 parts, was mixed at room temperature for 30 minutes and further mixed for 2 hours under a reduced pressure of 40mmHg while heating to 0.99 ° C..

  After cooling to room temperature, 2 parts of (F) diisopropoxybis (ethyl acetoacetate) titanium and 3 parts of (E) dimethyldimethoxysilane were added to the mixture and mixed until moisture became homogeneous.

The obtained composition was coated to a thickness of 2 mm on a glass plate having a width of 25 mm, a length of 80 mm, and a thickness of 5 mm, and cured at 23 ° C. and 50% RH for 3 days. Furthermore, about these, as shown in FIG. 1, rubber | gum and glass were peeled by the autograph and the interface peeling rate and peeling force at that time were evaluated.
Example 2
30 parts of the polymer (A) used in Example 1, 70 parts of the polymer (B), 5 parts of the silicone oil (C) and 10 parts of silica A were mixed for 30 minutes at room temperature, and further heated to 150 ° C. The mixture was mixed under a reduced pressure of 40 mmHg for 2 hours.

After cooling to room temperature, 2 parts of (F) diisopropoxybis (ethyl acetoacetate) titanium and 2 parts of (E) vinylmethyldimethoxysilane were added to the mixture and mixed until moisture became homogeneous. Evaluation similar to Example 1 was performed about the obtained composition.
Example 3
50 parts of polymer (A) used in Example 1, 50 parts of polymer (B), 10 parts of silicone oil (C) and dry silica (surface treated with dimethyldichlorosilane at a specific surface area of 170 m ² / g by BET method) 15 parts of carbon amount 1.0%: silica B) was mixed and mixed at room temperature for 30 minutes, and further mixed under reduced pressure of 40 mmHg for 2 hours while heating to 150 ° C.

After cooling to room temperature, 2 parts of (F) diisopropoxybis (ethyl acetoacetate) titanium and 3 parts of (E) dimethyldimethoxysilane were added to the mixture and mixed until moisture became homogeneous. Evaluation similar to Example 1 was performed about the obtained composition.
Comparative Example 1
A composition was prepared in the same manner as in Example 1 except that the silicone oil (C) was not blended and (E) methyltrimethoxysilane was used instead of dimethyldimethoxysilane, and the same evaluation as above was performed. . The results are shown in Table 1.
Comparative Example 2
In Example 1, a composition was prepared in the same manner except that 100 parts of the polymer (A) was used without using the polymer (B) and no silicone oil (C) was added, and the same evaluation as above was performed. The results are shown in Table 1.
Comparative Example 3
In Example 1, a composition was prepared in the same manner except that the silicone oil (C) was not blended, and the same evaluation as above was performed. The results are shown in Table 1.

It is a figure which shows the evaluation condition of the interface peeling rate and peeling force in an Example.

Claims (1)

(A) 5 to 95% by weight of polyorganosiloxane having a viscosity at 25 ° C. of 0.1 to 1000 Pa · s and both ends blocked with trialkoxysilyl groups
(B) Polyorganosiloxane having a viscosity at 25 ° C. of 0.1 to 1000 Pa · s and having both ends blocked with dialkoxymonoorganosilyl groups, 95 to 5% by weight
For 100 parts by weight of polyorganosiloxane consisting of
(C) 1-50 parts by weight of a polyorganosiloxane containing no silanol group, trialkoxy group and dialkoxy group in the molecule and having a viscosity at 25 ° C. lower than the viscosity of the component (A) and / or the component (B),
(D) 1 to 50 parts by weight of silica powder having a specific surface area of 50 m ² / g or more,
(E) 0.5 to 15 parts by weight of a bifunctional alkoxysilane or a partially hydrolyzed condensate thereof,
(F) A room temperature-curable polyorganosiloxane composition comprising 0.1 to 15 parts by weight of a titanium chelate catalyst.

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