Patent Application
20190390083
The present invention relates to a coating agent for concrete structures.
There is concern that portions of a concrete structure such as a tunnel inner wall or bridge girder may detach and fall as a result of surface cracking due to neutralization and internal cracking due to earthquakes, vibration, ground subsidence, overload, and the like, and may drop onto to a vehicle or navigating ship passing under the structure. Therefore, methods for coating a transparent or semi-transparent resin onto the surface of a concrete structure have been proposed (see Patent Documents 1 to 3).
As a coating agent used in such methods, an organic resin such as an epoxy resin, acrylic resin, urethane resin, or polyester resin is used.
However, the weather resistance of such an organic resin is poor, and therefore such an organic resin is insufficient as a coating agent for tunnels, bridge girders, and other such concrete structures that are exposed to harsh environments. On the other hand, a silicone rubber composition that is cured by moisture does not need to be heated or the like when curing, and a silicone cured product having excellent weather resistance can be formed, and therefore such compositions have been examined as coating agents for concrete structures. However, an issue with silicone rubber compositions is that adhesion to a concrete structure is insufficient.
An object of the present invention is to provide a coating agent for concrete structures, the coating agent forming a silicone film that is strongly adherent to a concrete structure, and that enables visual confirmation of the surface state of the concrete structure through the silicone film.
The coating agent for concrete structures of the present invention comprises:
(A) 100 parts by mass of a diorganopolysiloxane capped at both molecular terminals with silanol groups or silicon atom-bonded hydrolyzable groups;
(B) 1 to 25 parts by mass of a silane compound having at least two silicon atom-bonded hydrolyzable groups per molecule, or a partially hydrolyzed condensate thereof;
(C) 0.5 to 10 parts by mass of a curing catalyst; and
(D) 15 to 40 parts by mass of fumed silica.
The silicon atom-bonded hydrolyzable group in component (A) is preferably an alkoxy group.
Component (B) is preferably an alkoxysilane represented by the general formula:
R1aSi(OR2)(4-a)
(wherein, R1 is a monovalent hydrocarbon group having from 1 to 6 carbon atoms; R2 is an alkyl group having from 1 to 3 carbon atoms; and “a” is 0 or 1) or a partially hydrolyzed condensate thereof.
Component (C) is preferably an organic titanium compound.
Component (D) is preferably fumed silica obtained by surface treating fumed silica having a BET specific surface area of from 50 to 400 m2/g with an organosilicon compound.
The composition may further comprise (E) a desired amount of an organic solvent.
Moreover, a method for coating a concrete structure according to the present invention is characterized in that a primer is applied onto a surface of a concrete structure, after which a coating agent for concrete structures as described above is applied.
According to the coating agent for concrete structures of the present invention, a silicone film that is strongly adherent to a concrete structure is formed, and the surface state of the concrete structure can be visually confirmed through the silicone film.
The coating agent for concrete structures of the present invention will be described in detail.
Component (A) is a diorganopolysiloxane having silicon atom-bonded hydroxyl groups (so-called silanol groups) or silicon atom-bonded hydrolyzable groups at both molecular terminals. Examples of the silicon atom-bonded hydrolyzable groups include alkoxy groups such as a methoxy group, ethoxy group, and propoxy group; oxime groups such as an acetoxime group and a methylethylketoxime group; amino groups such as a dimethylamino group and a diethylamino group; amide groups such as an N-methylacetamide group; aminoxy groups such as a diethylaminoxy group; and alkenyloxy groups such as an isopropenyloxy group; and of these, alkoxy groups are preferable. Such alkoxy groups may be bonded directly to a silicon atom at each of the molecular terminals, and may be bonded to a silicon atom that is bonded to a silicon atom at the molecular terminal via an alkylene group. Examples of the alkylene group include a methylmethylene group, ethylene group, methylethylene group, and a propylene group. Examples of other groups bonded to the silicon atom in component (A) include alkyl groups such as a methyl group, ethyl group, propyl group, and butyl group; alkenyl groups such as a vinyl group and an allyl group; aryl groups such as a phenyl group, tolyl group, and naphthyl group; aralkyl groups such as a benzyl group, phenylethyl group, and phenyl propyl group; and halogenated hydrocarbon groups such as a chloromethyl group, trifluoropropyl group, and chloropropyl group; and of these, a methyl group is particularly preferable.
Component (B) is a silane compound having at least two silicon atom-bonded hydrolyzable groups per molecule, or is a partially hydrolyzed condensate thereof. Examples of the silicon atom-bonded hydrolyzable groups include alkoxy groups such as a methoxy group, ethoxy group, and propoxy group; oxime groups such as an acetoxime group and a methylethylketoxime group; amino groups such as a dimethylamino group and a diethylamino group; amide groups such as an N-methylacetamide group; aminoxy groups such as a diethylaminoxy group; and alkenyloxy groups such as an isopropenyloxy group; and of these, alkoxy groups are preferable. Examples of other groups bonded to the silicon atom in component (B) include alkyl groups such as a methyl group, ethyl group, propyl group, and butyl group; alkenyl groups such as a vinyl group and an allyl group; aryl groups such as a phenyl group, tolyl group, and naphthyl group; aralkyl groups such as a benzyl group, phenylethyl group, and phenylpropyl group; and halogenated hydrocarbon groups such as a chloromethyl group, trifluoropropyl group, and chloropropyl group; and of these, a methyl group is particularly preferable.
Component (B) is preferably an alkoxysilane represented by the general formula:
R1aSi(OR2)(4-a)
or is a partial hydrolysate thereof. In the formula, R1 is a monovalent hydrocarbon group having from 1 to 6 carbon atoms, and examples include: an alkyl group such as a methyl group, ethyl group, propyl group, or butyl group; an alkenyl group such as a vinyl group or allyl group; and a phenyl group. Furthermore, in the formula, R2 is an alkoxy group having from 1 to 3 carbon atoms, and examples include a methoxy group, an ethoxy group, and a propoxy group. In the formula, “a” is 0 or 1.
Examples of the alkoxysilane for component (B) include methyl trimethoxysilane, methyl triethoxysilane, ethyl trimethoxysilane, vinyl trimethoxysilane, phenyl trimethoxysilane, methyl trimethoxyethoxy silane, tetramethoxysilane, and tetraethoxysilane; examples of oxime silanes for component (B) include methyl tris(methylethylketoxime) silane and vinyl tris(methylethylketoxime) silane; examples of the aminosilane for component (B) include methyl tris(dimethylamino) silane; examples of the amide silane for component (B) include methyl tris(N-methylacetamide) silane;
and examples of the aminoxysilane for component (B) include methyl tris(dimethylaminoxy) silane. Component (B) may use these compounds independently or as a mixture of two or more types thereof.
The content of component (B) is within a range of from 1 to 25 parts by mass, and preferably within a range of from 2 to 10 parts by mass, per 100 parts by mass of component (A). This is because when the content of component (B) is not less than the lower limit of the aforementioned range, the storage stability of the coating agent improves, and on the other hand, when the content is not more than the upper limit of the aforementioned range, the curability of the coating agent improves.
Component (C) is a curing catalyst, and examples include organic titanium compounds and organic tin compounds. Examples of the organic titanium compounds include tetra(i-propoxy) titanium, tetra(n-butoxy) titanium, tetra(t-butoxy) titanium, and other titanates; di(i-isopropoxy) bis(ethyl acetoacetate) titanium, di(i-propoxy) bis(methylacetoacetate) titanium, di(i-propoxy) bis (acetylacetone) titanium, and other titanium chelates. Examples of the organic tin compounds include dibutyltin dilaurate, dibutyltin diacetate, and dibutyltin dioctoate.
The content of component (C) is within a range of from 0.5 to 10 parts by mass, and preferably within a range of from 1 to 5 parts by mass, per 100 parts by mass of component (A). This is because when the content of component (C) is not less than the lower limit of the aforementioned range, curability of the coating agent is promoted, and on the other hand, when the content is not more than the upper limit of the aforementioned range, the storage stability of the coating agent improves.
Component (D) is fumed silica for improving the adhesion of the present coating agent and improving the mechanical properties of the obtained silicone film. This type of component (D) is preferably fumed silica obtained by surface treating with an organosilicon compound fumed silica having a BET specific surface area within a range of from 50 to 400 m2/g, within a range of from 100 to 400 m2/g, or within a range of from 200 to 400 m2/g. Examples of the organosilicon compound include hexamethyldisilane, hexamethylcyclotrisilazane, and other such silazane compounds; trimethylchlorosilane, dimethyldichlorosilane and other such halosilane compounds; methyltrimethoxysilane, dimethyldimethoxysilane, and other such alkoxysilane compounds; and methylhydrogenpolysiloxane and other such organopolysiloxanes.
The content of component (D) is within a range of from 15 to 40 parts by mass, and preferably within a range of from 20 to 40 parts by mass, within a range of from 25 to 40 parts by mass, or within a range of from 30 to 40 parts by mass, per 100 parts by weight of component (A). This is because when the content of component (D) is not less than the lower limit of the aforementioned range, the adhesiveness of the coating agent improves, and on the other hand, when the content is not more than the upper limit of the aforementioned range, the ease of applying the coating agent improves.
The present coating agent may comprise, for example, an organic solvent, an anti-mold agent, a flame retardant, a heat resistance agent, a plasticizer, a thixotropy-imparting agent, an adhesion imparting agent, a curing accelerator, and a pigment within a range that does not hinder the object of the present invention. Examples of the organic solvent include normal hexane, toluene, xylene, and cellosolve acetate, the compounded amount thereof is optional, and a desired amount can be compounded with consideration of the ease of applying the present coating agent and the film thickness of the resulting silicone film.
Examples of the concrete structure to which the coating agent is applied include a road or rail tunnel, a road or rail bridge, and the like.
Next, as illustrated in
Note that a reticulated flaking prevention material can be disposed on the surface of the primer layer 2 in a layered manner to improve the concrete flaking off prevention performance. The flaking prevention material is not limited, and sheets (planar shaped bodies) of various shapes such as woven sheet-like sheets (such as fiber sheets), nonwoven sheets, and net-like or mesh-like sheets (sometimes referred to as “net-like sheets”) can be used. Furthermore, various fibers such as carbon fibers, plastic fibers (e.g. aramid fibers, vinylon fibers, polyethylene fiber sheets (in particular, fiber sheets made of high impact type polyethylene), and polyimide fiber sheets, etc.), and glass fibers can be used as the material for flaking prevention.
The coating agent for a concrete structure of the present invention will be described in detail using Examples. Note that the viscosity is a value at 25° C. Furthermore, the adhesive strength of the cured product of the coating agent with respect to the concrete structure, and the visibility of the cured product were evaluated as follows.
[Adhesion]
The adhesion of the cured product of the coating agent to the concrete structure was evaluated through the following “Method for Testing the Adhesion Strength of a Surface Coating Material.”
[Method for Testing the Adhesion Strength of a Surface Coating Material]
The adhesion strength was measured in accordance with the provisions of JSCE-K 531-2013 “Method for Testing Adhesion Strength of a Surface Coating Material” of the Standard Specifications for Concrete Structure published by the Japan Society of Civil Engineers. Specifically, the measurements were performed as follows. A concrete test piece having an inner dimension of 70 mm×70 mm×20 mm was used in accordance with the method stipulated by JIS R5201 10.4. A primer (a sealant primer B available from Dow Corning Toray Co., Ltd.) was applied at 100 g/m2 and dried on the concrete test piece. Subsequently, the coating agent was applied and cured for 14 days in a 23±2° C., 50±5% RH environment in accordance with the curing conditions stipulated by JIS A 1439, and then cured for 14 days in an oven at 30±2° C. To the surface of the obtained test piece, an upper tensioning steel jig as stipulated by JSCE-K 531-2013 was adhered to the surface of the cured product of the coating agent using an adhesive (Cemedine PPX), and then left to sit for 24 hours in a 23±2° C., 50±5% RH atmosphere. Next, a square notch of 40 mm×40 mm was inserted as far as a substrate around the upper tensioning steel jig adhered to the test piece. The maximum tensile load (N/mm2) was determined by using a steel jig for a lower tensile test and a steel contact plate described in JSCE-K 531-2013, and applying a tensile force using an autograph (available from Shimadzu Corporation) in the vertical direction. Note that the loading rate until breakage was 1750 N/minutes.
[Visibility]
The ability to confirm the surface state of the concrete test piece through the cured product of the coating agent was evaluated, and cases in which confirmation was possible were indicated by “∘”, cases in which confirmation was difficult were indicated by “Δ”, and cases in which confirmation was not possible were indicated by “x”.
A silicone rubber base compound was prepared by mixing 100 parts by mass of a dimethylpolysiloxane capped at both molecular terminals with hydroxy groups and having a viscosity of 15,000 mPa·s, and 35 parts by mass of fumed silica obtained by surface treating fumed silica having a BET specific surface area of 220 m2/g with hexamethyldisilazane. Next, under moisture blocking, a coating agent (I) for concrete structures was prepared by mixing 10 parts by mass of methyltrimethoxysilane and 0.7 parts by mass of tetra(t-butoxy)titanium with this silicone rubber base compound. The coating agent was then applied to a concrete test piece at a thickness of 1.0 mm to produce a test piece. The evaluation results are shown in Table 1.
A solvent type coating agent (II) for concrete structures was prepared by blending 100 parts by mass of the coating agent (I) for concrete structures prepared in Example 1 with 100 parts by mass of normal hexane. The coating agent was then applied to a concrete test piece at a thickness of 0.5 mm to produce a test piece. The evaluation results are shown in Table 1.
A coating agent (III) for concrete structures was prepared in the same manner as in Example 1 with the exception that the compounded amount of fumed silica was changed to 10 parts by mass. The coating agent was then applied to a concrete test piece at a thickness of 1.0 mm to produce a test piece. The evaluation results are shown in Table 1.
When the compounded amount of the fumed silica of Example 1 was changed to 45 parts by mass, a uniform base compound could not be prepared, and thus a uniform coating agent could not be prepared.
A base compound was prepared by mixing 100 parts by mass of a dimethylpolysiloxane capped at both molecular terminals with hydroxy groups and having a viscosity of 15,000 mPa·s, and 17 parts by mass of precipitated calcium carbonate (Solvay SA product name: Socal 312 N) that had been treated with stearic acid. Next, under moisture blocking, a coating agent (IV) for concrete structures was prepared by mixing 10 parts by mass of methyltrimethoxysilane and 0.7 parts by mass of tetra(t-butoxy)titanium with this base compound. The coating agent was then applied to a concrete test piece at a thickness of 1.0 mm to produce a test piece. The evaluation results are shown in Table 1.
Because the coating agent for concrete structures of the present invention is cured by moisture to form a silicone film having high weather resistance, the coating agent of the present invention is suitable as a coating agent for tunnels, bridge girders, and other such concrete structures that are exposed to harsh environments.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2017-014690 | Jan 2017 | JP | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/JP2018/001722 | 1/22/2018 | WO | 00 |
