KR20100006351A - Non-slip agent composition, non-slip paving process using the same and non slip paving structure of the same - Google Patents

Abstract

PURPOSE: A non-slip agent composition is provided to effectively prevent slipping and enhance adhesive force of asphalt road surface and non-slip paving, and to enable quick hardening of non-slip paving at a room temperature. CONSTITUTION: A non-slip agent composition comprises a resin part, a curing accelerator part, and a hardener part. The resin part comprises methyl methacrylic acid 30.0-40.0 wt%, styrene monomer 20.0-29.95 wt% and reactive inhibitor 0.01-0.05 wt%. The curing accelerator part includes urethane prepolymer 7.0-17.0 wt%, methyl methacrylic acid 5.0-12.0 wt% and 4,4-phenylmethane diisocynate 1.0-5.0 wt%. The hardener part comprises benzoyl peroxide.0-4.0 wt% and dioctylphthalate 1.0-2.0 wt%.

Description

Non-slip agent composition, non-slip paving process using the same and non-slip paving process using the same and non slip paving structure of the same}

The present invention relates to an anti-slip agent composition, an anti-slip packing method and a non-slip packing structure using the same, and more particularly, to effectively prevent slip, while the anti-slip agent composition for strengthening the adhesion between the asphalt road surface and the anti-slip pavement, using the same An anti-slip packaging method and a non-slip packaging structure.

Generally, slope roads, winding roads and school zones are provided with anti-skid pavement to prevent vehicle speeding and for effective braking. The anti-slip pavement protrudes from the road surface to increase the contact resistance with the vehicle wheels, preventing overspeed of the vehicle or ventilating the surroundings.

The anti-slip package is protruded to increase contact resistance with the wheels, and also uses an anti-slip agent. The anti-slip agent forming the anti-slip package has the effect of shortening the braking distance by increasing the contact resistance with the wheels.

In order to achieve such an effect, the anti-slip agent must be attached to the asphalt road surface with strong adhesion to maintain the adhesion state without peeling off the asphalt road surface.

The anti-slip agent also needs to be cured quickly at renovation of the anti-slip package at room temperature to enable resumption of vehicle traffic.

On the other hand, since the antislip agent causes a chemical reaction even in an extremely low temperature environment or an extremely high temperature environment, it is required to be cured to enable the repair of the flooring material of the refrigeration and cold storage warehouses or the hot water supply tank of the production line.

One embodiment of the present invention relates to a non-slip agent composition for strengthening the adhesion between the asphalt road surface and the anti-skid pavement, while effectively preventing slip, a non-slip pavement method using the same and a non-slip pavement structure.

One embodiment of the present invention relates to an anti-slip agent composition that enables rapid curing of an anti-slip package at room temperature, an anti-slip packaging method using the same, and a non-slip packaging structure.

In addition, an embodiment of the present invention relates to an anti-slip agent composition that is cured in extreme environments of high temperature and low temperature to form an anti-slip package, an anti-slip packaging method using the same and a non-slip packaging structure.

The anti-slip agent composition according to an embodiment of the present invention comprises a resin portion, a curing accelerator portion and a curing agent portion, wherein the resin portion in weight percent of styrene monomer 30.0-40.0, methylmethacrylic acid 25.0-29.95 and reaction inhibitor 0.01- 0.05, wherein the curing accelerator portion comprises urethane prepolymer 7.0-17.0, methylmethacrylic acid 5.0-12.0 and 4.4 phenylmethadiisocyanate 1.0-5.0, the curing agent portion benzoylperoxide 3.0-4.0 and dioctylphthalate 1.0 May include -2.0.

The anti-slip agent composition according to an embodiment of the present invention includes a resin portion, a powder portion and a curing agent portion, and the resin portion in weight% of methylmethacrylic acid 10.0-16.0, normal butylmethacrylic acid 8.0-14.0, styrene monomer 2.0-5.0 and 0.01-0.05 reaction inhibitor, wherein the powder portion comprises a self-horizontal mortar 60.0-80.0 and coloring pigment 0.5-2.5, the hardener portion is benzoyl peroxide 0.5-1.0 and dioctylphthalate 0.2-0.5 It may include.

In the anti-slip paving method according to an embodiment of the present invention, applying a primer formed of the anti-slip agent composition on the asphalt road surface to form a primer layer, applying a middle material to the primer layer to form a middle layer layer And, it may include the step of forming a top coat material by applying a top coat material to the intermediate material layer.

The intermediate material layer forming step may be formed by applying the intermediate material formed of the anti-slip agent composition to form the intermediate material layer.

The intermediate material layer forming step may be applied by mixing the silica sand to the intermediate material.

The top coat comprises a resin portion, a powder portion and a hardener portion, the resin portion by weight of the resin portion contains methyl methacrylate 70.0-82.0, dioctylphthalate 4.0-9.0 and styrene monomer 0.5-5.0, the powder portion is a pigment pigment 5.9-11.0, and the curing agent portion may include benzoyl peroxide 1.5-3.0 and dioctylphthalate 0.5-2.0.

In addition, the anti-slip packaging structure according to an embodiment of the present invention, may be made of the anti-slip agent composition or packaging method.

As such, according to an embodiment of the present invention, since the adhesion between the asphalt road surface and the anti-skid pavement is increased, the anti-skid pavement is prevented from peeling from the asphalt road surface, thereby maintaining the anti-slip continuously.

According to an embodiment of the present invention, since the primer layer is formed on the asphalt road surface, and the middle layer and the top layer are sequentially formed on the primer layer, the primer layer and the middle layer are prevented from being peeled from the asphalt road surface, thereby preventing slippage. It is effective to maintain.

According to one embodiment of the present invention, because it contains a curing accelerator to quickly cure at room temperature to enable rapid curing of the anti-skid packaging, and because it contains benzoyl peroxide in the curing agent is cured in extreme environments of high and low temperature anti-slip packaging There is an effect that enables the formation of.

Hereinafter, exemplary embodiments of the present invention will be described in detail with reference to the accompanying drawings so that those skilled in the art may easily implement the present invention. As those skilled in the art would realize, the described embodiments may be modified in various different ways, all without departing from the spirit or scope of the present invention. In the drawings, parts irrelevant to the description are omitted in order to clearly describe the present invention, and like reference numerals designate like elements throughout the specification.

1 is a flow chart of a non-slip packaging method according to an embodiment of the present invention. For convenience, the anti-slip packaging method and the non-slip packaging structure will be described in parallel.

Anti-skid paving method of an embodiment is a primer layer (2) forming step (ST1), the intermediate material layer (3) forming step (ST2) and the top coat layer (4) formed sequentially on the asphalt road surface (1) or concrete ground surface Step ST3 is included.

The anti-skid pavement structure formed by this method includes the primer layer 2, the intermediate material layer 3, and the top coat layer 4, which are formed in a laminated structure on the asphalt road surface 1 or the concrete base surface.

In the forming of the primer layer 2 (ST1), the primer layer 2 is formed by applying a primer formed of the anti-slip agent composition of the embodiment to the asphalt road surface 1.

The primer layer 2 exerts a strong adhesive force between the non-slip pavement including the primer layer 2 and the asphalt road surface 1, thereby preventing the peeling of the non-slip pavement. In other words, the primer layer 2 is bonded to the asphalt road surface 1 with strong adhesion.

The intermediate material layer 3 forming step ST2 is applied to the primer layer 2 to form the intermediate material layer 3 by applying the intermediate material formed of the anti-slip agent composition of one embodiment. The intermediate material layer 3 is the part which forms most of the protrusion height in an anti-slip package, and is responsible for most of an anti-slip action in an anti-slip package.

The intermediate material layer 3 forming step ST2 is applied by mixing the silica sand 31 with the intermediate material. Therefore, the intermediate layer 3 is formed by including the silica sand 31 in the intermediate material further enhances the braking force of the wheel.

In the forming of the top coat layer 4 (ST3), the top coat material formed of the anti-slip agent composition of the embodiment is applied to the middle coat layer 3 to form the top coat layer 4.

The top coat layer 4 prevents the aging of the middle coat layer 3 in addition to the anti-slip action, and includes a color pigment, thereby improving visibility and drawing attention.

First, the anti-slip agent composition which forms the primer layer 2 is demonstrated.

Composition of the primer Composition Content (% by weight) Resin Reaction inhibitor 0.01-0.05 Methylmethacrylic acid 30.0-40.0 Styrene monomer 20.0-29.95 Hardening accelerator part Methylmethacrylic acid 5.0-12.0 4.4 phenylmeta diisocyanate 1.0-5.0 Urethane Prepolymer 7.0-17.0 Curing agent part Benzoyl peroxide 3.0-4.0 Dioctylphthalate 1.0-2.0

The primer of one embodiment includes a resin portion, a curing accelerator portion, and a curing agent portion, representing each composition in weight percent. The resin portion contains methylmethacrylic acid 30.0-40.0, styrene monomer 20.0-29.95 and reaction inhibitor 0.01-0.05, and the curing accelerator portion is urethane prepolymer 7.0-17.0, methylmethacrylic acid 5.0-12.0 and 4.4 phenylmethadiisocyanate 1.0 -5.0, and the curing agent portion includes benzoylperoxide 3.0-4.0 and dioctylphthalate 1.0-2.0.

For example, if methylmethacrylic acid is less than 30.0, weather resistance will fall, and if it is more than 40.0, economic efficiency will fall. If the reaction inhibitor is less than 0.01, gelation may proceed during storage, and if it is more than 0.05, coating film formation becomes difficult. If the urethane prepolymer is less than 7.0, it is difficult to form a soft coating film, and if it is more than 17.0, the coating film strength becomes too weak. When methylmethacrylic acid is less than 5.0, weather resistance falls, and when it is more than 12.0, economic efficiency falls. When the phenyl methadiisocyanate is less than 1.0, coating film formation is difficult, and when it is more than 5.0, the curing speed is too fast, and normal operation is difficult. When benzoyl peroxide is less than 3.0, workability | operativity falls by delay of drying time, and when it exceeds 4.0, hardening rate is too fast and normal operation | work is difficult. When dioctyl phthalate is less than 1.0, the storage property of a hardening | curing agent falls, and when it is more than 2.0, drying time is delayed.

The resin portion forms a strong adhesion when applied to the asphalt road surface 1 and the concrete ground surface. The curing accelerator part enables rapid curing of the primer at room temperature and stabilizes physical properties. The hardener portion causes chemical reactions at low and high temperatures to enable curing.

Examples of the preparation of the primer can be given. First, the resin part will be described. Into a reaction vessel equipped with a propeller-type stirrer, 0.02% by weight of methyl alcohol solution of 30.0% by weight of methylmethacrylic acid and 0.1% by weight of hydroquinone was added as a reaction inhibitor, and stirred at 100 rpm for 10 minutes for 20 ±. Circulate cooling water cooled to 5 ° C.

15.0% by weight of styrene monomer is added and 15% by weight of the remaining styrene monomer is gradually added while the mixture is kept at a temperature not exceeding 35 ° C while stirring, and then cooled to 30 ° C or lower, and the finished mixture, that is, the resin part, is designated Pack in.

A hardening accelerator part is demonstrated. 9.0% by weight of methylmethacrylic acid is added to a reaction vessel with a cooling condenser, and 13.0% by weight of urethane prepolymer is gradually added while stirring at 100 rpm to maintain the temperature of the mixture not to exceed 40 ° C.

After the addition, the mixture was stirred for 20 minutes, and 3.0 wt% of 4.4phenylmethadiisocyanate was added in a titration manner to sufficiently supply cooling water to maintain the temperature at 40 ° C or lower. The temperature is cooled below 30 ° C. and the finished mixture, ie, the curing accelerator portion, is packaged in the designated container.

A hardening | curing agent part is demonstrated. 1.5% by weight of dioctylphthalate is added to the reaction vessel, and 3.5% by weight of benzoyl peroxide is gradually added to sufficiently immerse in dioctylphthalate, and the finished mixture, i.e., the curing agent portion, is packaged in a designated container.

In the forming of the primer layer 2 (ST1), the asphalt road surface 1 or the concrete ground surface is divided in units of 30 m 2 before the resin part, the curing accelerator part, and the curing agent part are mixed to determine the application order.

75 weight% of a resin part and 25 weight% of a hardening accelerator part are mixed to a container, it mixes for 1 minute with an electric stirrer, 5 weight% of hardening | curing agent parts are thrown in, and it mixes for 30 second.

The mixed resin part is applied to a designated section using a brush or a roller. Since the available time of the primer is about 10 minutes at 25 ℃, the entire amount should be applied within this time. When the available time is exceeded, the primer which is gelatinizing is used, and the adhesive force with the asphalt road surface 1 may fall.

The slipper composition which forms the intermediate material layer 3 is demonstrated.

Composition of intermediate materials Composition Content (% by weight) Resin Reaction inhibitor 0.01-0.05 Methylmethacrylic acid 10.0-16.0 Normal Butyl Methacrylic Acid 8.0-14.0 Styrene monomer 2.0-5.0 Powder Self-Horizontal Mortar 60.0-80.0 Pigmentation Pigment 0.5-2.5 Curing agent part Benzoyl peroxide 0.5-1.0 Dioctylphthalate 0.2-0.5

The intermediate material of one embodiment includes a resin part, a powder part, and a hardener part, and each composition is represented by weight%. The resin part contains methylmethacrylic acid 10.0-16.0, normal butylmethacrylic acid 8.0-14.0, styrene monomer 2.0-5.0 and reaction inhibitor 0.01-0.05, and the powder part is self-horizontal mortar 60.0-80.0 and coloring pigment 0.5-2.5 It includes, and the curing agent portion includes benzoyl peroxide 0.5-1.0 and dioctylphthalate 0.2-0.5.

For example, when methylmethacrylic acid is less than 10.0, weather resistance falls, and when it exceeds 16.0, economic efficiency falls. When normal butyl methacrylic acid is less than 8.0, coating film strength falls, and when it is more than 14.0, coating film becomes hard more than necessary. If the styrene monomer is less than 2.0, the economical efficiency is lowered due to the addition of other components, and if it is more than 5.0, the weather resistance is lowered. If the reaction inhibitor is less than 0.01, gelation may proceed during storage, and if it is more than 0.05, coating film formation becomes difficult. When the self-horizontal mortar is less than 60.0, it is difficult to secure the coating film thickness, and when the self-horizontal mortar is more than 80.0, a cracking shape occurs during coating film formation. If the coloring pigment is less than 0.5, it is difficult to achieve the desired color, if it is more than 2.5, the economic efficiency is lowered. When benzoyl peroxide is less than 0.5, workability | operativity falls by delay of drying time, and when it exceeds 1.0, hardening rate is too fast and normal operation | work is difficult. When dioctyl phthalate is less than 0.2, the storage property of a hardening | curing agent falls, and when it is more than 0.5, drying time is delayed.

The resin portion forms a strong adhesion with the primer layer 2 when the intermediate material is applied to the primer layer 2. The powder portion forms the protruding height of the anti-slip package, and acts as a slip. The hardener portion causes chemical reactions at low and high temperatures to enable curing.

Examples of the intermediate material may be mentioned. First, the resin part will be described. Into a reaction vessel equipped with a propeller-type stirrer, 12.0% by weight of methylmethacrylic acid, 10.0% by weight of normal butylmethacrylic acid, and 0.02% by weight of a methyl alcohol solution dissolved in 0.1% by weight of hydroquinone were added as a reaction inhibitor, and 10 rpm at 100 rpm. Cooling water is injected to the outside of the reaction vessel with stirring for a minute, and the temperature of the mixture is maintained at 40 ° C or lower.

While slowly adding the styrene monomer in a dropwise manner of 5.0% by weight, the mixture is stirred for 30 minutes while maintaining the temperature of the mixture at 35 ° C. or lower, thereby packing the finished mixture, that is, the resin part, in a designated container.

The powder part will be described. 70.0% by weight of self-horizontal mortar and 2.0% by weight of pigment are uniformly mixed in a powder mixer for 30 minutes and packaged in a designated bag by designated amount.

For example, the coloring pigment uses inorganic pigments such as iron oxide red, iron oxide black, titanium dioxide, chromium yellow and chromium oxide green. When using an inorganic pigment, the preparation pigment which premixed the organic pigment of 20 weight% or less with 80 weight% of barium sulfate can be used limitedly.

A hardening | curing agent part is demonstrated. 0.5% by weight of dioctylphthalate is added to the reaction vessel, 0.4% by weight of benzoyl peroxide is gradually added to sufficiently wet the dioctylphthalate, and the finished mixture, i.e., the curing agent portion, is packaged in a designated container.

In the intermediate material layer (3) forming step (ST2), 30 minutes after applying the primer layer (3), the surface of the primer layer (3) can be seen that the curing is completed, the finger presses the primer layer (3) If no fingerprints remain on the surface, the intermediate material can be applied.

In the step of forming the intermediate material layer 3 (ST2), 72.02% by weight of the resin part and 72% by weight of the powder part are mixed in a container, and mixed for 3 minutes with an electric stirrer to sufficiently loosen the powder part without agglomeration. 0.9 weight% of the curing agent is further added and stirred for 30 seconds.

The silica sand 31 is further mixed with the mixed intermediate material, and applied to the primer layer 2 to have a thickness of 1 mm or more by using a brush or a paper.

Since the usable time of the intermediate material is about 20 minutes at 25 ° C., the mixing amount of the intermediate material is mixed and used in an amount that can be applied within 20 minutes. When the available time is exceeded, the intermediate material in which gelation is in progress will be used, and the adhesive force with the primer layer 2 may fall.

The slipper composition which forms the top coat layer 4 is demonstrated.

Composition of Top Coating Composition Content (% by weight) Resin Methylmethacrylic acid 70.0-82.0 Dioctylphthalate 4.0-9.0 Styrene monomer 0.5-5.0 Powder Coloring pigment 5.9-11.0 Curing agent part Benzoyl peroxide 1.5-3.0 Dioctylphthalate 0.5-2.0

The coating material of one embodiment includes a resin part, a powder part, and a hardener part, and represents each composition by weight. The resin portion contains methylmethacrylic acid 70.0-82.0, dioctylphthalate 4.0-9.0 and styrene monomer 0.5-5.0, the powder portion contains colored pigment 5.9-11.0, and the hardener portion benzoyl peroxide 1.5-3.0 and dioctylphthalate 0.5-2.0.

For example, when methylmethacrylic acid is less than 70.0, weather resistance falls, and when it is more than 82.0, economic efficiency falls. When dioctyl phthalate is less than 4.0, a coating film becomes hard more than necessary, and when it is more than 9.0, a coating film becomes soft too much. If the styrene monomer is less than 0.5, the economical efficiency is lowered due to the addition of other components, and if it is more than 5.0, the weather resistance is lowered. If the colored pigment is less than 5.9, it is difficult to achieve the desired color, if it is more than 11.0, the economic efficiency is lowered and the coating film properties are lowered. When benzoyl peroxide is less than 1.5, workability | operativity falls by delay of drying time, and when it exceeds 3.0, hardening rate is too fast and normal operation | work is difficult. When dioctyl phthalate is less than 0.5, the storage property of a hardener falls, and when it is more than 2.0, drying time is delayed.

Since the resin portion is applied to the intermediate material layer 3, it is attached to the intermediate material layer 3 to protect the intermediate material layer 3. The powder part is made of colored pigments to improve the visibility of the top coat and the anti-slip package. The hardener portion causes chemical reactions at low and high temperatures to enable curing.

Examples of the production of a top coat are mentioned. First, the resin part will be described. Into a reaction vessel equipped with a propeller-type stirrer, 80.0% by weight of methylmethacrylic acid and 5.0% by weight of dioctylphthalate are added, followed by stirring at 200 rpm for 30 minutes. Cooling water is injected into the outside of the reaction vessel, and the mixture is maintained at 50 ° C. or lower while styrene monomer is added in a 2.0% by weight drop. The mixture is stirred for 30 minutes while maintaining the temperature of the mixture at 50 ° C. or lower. Cool to 30 ° C. or lower and package the finished mixture, ie the resin part, in a designated container.

The powder part will be described. The colored pigment is divided into plastic bags and sealed in units of 1 kg. For example, colored pigments include general inorganic pigments, but do not include inorganic pigments based on molybdenum. Inorganic pigments may cause aggregation when used.

A hardening | curing agent part is demonstrated. 1.0% by weight of dioctylphthalate is added to the reaction vessel, and 2% by weight of benzoyl peroxide is gradually added to be sufficiently wetted with dioctylphthalate, and the finished mixture, that is, the hardener portion, is packaged in a designated container.

In the step of forming the top coat layer 4 (ST3), when 50 minutes have elapsed after the middle coat layer 3 has been applied, it can be seen that the hardening of the surface of the middle coat layer 3 is completed, and the finger presses the middle coat 3. If no fingerprints remain on the surface, a top coat can be applied.

In the step of forming the top material layer 4 (ST3), 87.0% by weight of the resin part and 10% by weight of the powder part are mixed in a container and sufficiently stirred by an electric stirrer to release the powder parts from agglomeration. 3 weight% of the curing agent portion is further added and stirred for 30 seconds.

After stirring, it is applied onto the intermediate material layer 3 using a brush or a roller.

Since the usable time of the top coat is about 15 minutes at 25 ° C., the mixed amount of the top coat is mixed and used in an amount that can be applied within 15 minutes. When the available time is exceeded, the coating material in which gelation is advanced is used, the adhesive force with the intermediate material layer 3 falls, and peeling phenomenon appears.

Although one embodiment of the present invention has been described above, the present invention is not limited thereto, and various modifications and changes can be made within the scope of the claims and the detailed description of the invention and the accompanying drawings. Naturally, it belongs to the scope of the invention.

1 is a flow chart of a non-slip packaging method according to an embodiment of the present invention.

<Explanation of symbols for the main parts of the drawings>

1: asphalt road surface 2: primer layer

3: middle layer 4: upper layer

31: silica sand

Claims (7)

Including the resin portion, the curing accelerator portion and the curing agent portion, in weight percent The resin portion contains methylmethacrylic acid 30.0-40.0, styrene monomer 20.0-29.95 and the reaction inhibitor 0.01-0.05, Wherein the curing accelerator part comprises urethane prepolymer 7.0-17.0, methylmethacrylic acid 5.0-12.0 and 4.4 phenylmethadiisocyanate 1.0-5.0, The anti-slip agent composition comprising the benzoyl peroxide 3.0-4.0 and dioctylphthalate 1.0-2.0. Including resin part, powder part and hardener part, The resin portion contains methylmethacrylic acid 10.0-16.0, normal butylmethacrylic acid 8.0-14.0, styrene monomer 2.0-5.0 and reaction inhibitor 0.01-0.05, The powder part comprises a self-horizontal mortar 60.0-80.0 and a pigment pigment 0.5-2.5, The anti-slip agent composition comprising the hardener portion benzoyl peroxide 0.5-1.0 and dioctylphthalate 0.2-0.5. Forming a primer layer by applying a primer formed of the anti-slip agent composition of claim 1 to the asphalt road surface; Applying a middle material to the primer layer to form a middle material layer; And Slipper packaging method comprising the step of forming a top coat layer by applying a top coat material to the middle material layer. The method of claim 3, wherein The intermediate material layer forming step, An anti-slip agent packaging method of applying the intermediate material formed of the anti-slip agent composition of claim 2 to form the intermediate material layer. The method of claim 4, wherein The intermediate material layer forming step, An anti-slip agent packaging method of mixing and applying silica sand to the intermediate material. The method of claim 5, The top coat comprises a resin portion, a powder portion and a curing agent portion, in weight percent The resin portion contains methylmethacrylic acid 70.0-82.0, dioctylphthalate 4.0-9.0 and styrene monomer 0.5-5.0, The powder portion comprises a colored pigment 5.9-11.0, The hardener portion anti-skid packaging method comprising benzoyl peroxide 1.5-3.0 and dioctylphthalate 0.5-2.0. An anti-slip packaging structure comprising the anti-slip composition or packaging method of any one of claims 1 to 6.

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