JP5092811B2 - Foamed cosmetics - Google Patents

Description

  The present invention relates to a novel foamed decorative material. In particular, it retains excellent compression recovery even when foamed at a high magnification, and can recover from the weight of the product itself during storage, dents due to roller pressing during construction, or crushing due to traces after installation, and embossing It is related to a foamed decorative material that does not impair the design properties of the material, and is useful as an interior material of a building.

Conventionally, Patent Document 1 discloses a resin composition for foamed decorative materials comprising an aqueous emulsion containing an ethylene / vinyl ester copolymer, a thermally expandable microcapsule foaming agent, and an inorganic filler.
However, when the present inventors examined the high foaming ratio decorative material of 6.0 to 8.0 times using the technique described in the above-mentioned publication, the problem that the compression recovery property is not sufficient is apparent. became. When used as wallpaper, the compression recovery property represents the weight of the wallpaper product itself at the time of storage, or the recovery from crushing due to dents due to roller pressing during construction or after placement after construction.
JP 2003-13396 A

  The present invention has been made paying attention to the above-mentioned problems in the prior art, and the problem is that the product is excellent in compression recovery when foamed at a high magnification, and is a product at the time of storage. An object of the present invention is to provide a foamed cosmetic material that can recover against its own weight, or a dent caused by pressing a roller during construction or crushing caused by a placement mark after construction, and that does not impair the design properties due to embossing.

The invention according to claim 1 is a foamed decorative material obtained by heating and foaming a resin composition containing at least an aqueous emulsion resin, a thermally expandable microcapsule foaming agent, and an inorganic filler, and the thermally expandable material. The microcapsule foaming agent is composed of two kinds of a thermally expandable microcapsule foaming agent a and a thermally expandable microcapsule foaming agent b.
The heat-expandable microcapsule foaming agent a has an average particle diameter of 5 to 35 μm, an included gas amount of 10 to 35%, and a shell film thickness at the time of maximum foaming of 0.03 to 0.10 μm.
The heat-expandable microcapsule foaming agent b has an average particle diameter of 5 to 35 μm, an amount of encapsulated gas of 10 to 35%, and a shell film thickness at the time of maximum foaming of 0.10 to 0.25 μm.
This is a foamed decorative material.

  According to a second aspect of the present invention, there is a total of 2 to 2 of the thermally expandable microcapsule foaming agent a and the thermally expandable microcapsule foaming agent b with respect to 100 parts by weight of the aqueous emulsion resin. The foamed decorative material according to claim 1, comprising 30 parts by weight and 20 to 200 parts by weight of the inorganic filler.

  The invention according to claim 3 is characterized in that the content ratio a / b of the thermally expandable microcapsule foaming agent a and the thermally expandable microcapsule foaming agent b is 8/2 to 2/8. It is a foaming cosmetic material in any one of Claim 1 or 2.

The invention according to claim 4 is a surface of a foamed cosmetic material obtained by heating and foaming a resin composition containing at least the aqueous emulsion resin according to claim 1 , a thermally expandable microcapsule foaming agent, and an inorganic filler. Further, it is a foamed decorative material formed by pressing an embossed plate to form an uneven pattern .

The invention according to claim 1 is a foamed decorative material obtained by heating and foaming a resin composition containing at least an aqueous emulsion resin, a thermally expandable microcapsule foaming agent, and an inorganic filler, and the thermally expandable material. The microcapsule foaming agent is composed of two kinds of a thermally expandable microcapsule foaming agent a and a thermally expandable microcapsule foaming agent b.
The heat-expandable microcapsule foaming agent a has an average particle diameter of 5 to 35 μm, an included gas amount of 10 to 35%, and a shell film thickness at the time of maximum foaming of 0.03 to 0.10 μm.
The heat-expandable microcapsule foaming agent b has an average particle diameter of 5 to 35 μm, an amount of encapsulated gas of 10 to 35%, and a shell film thickness at the time of maximum foaming of 0.10 to 0.25 μm.
This is a foamed decorative material.
According to the invention of claim 1, it is possible to provide a foamed decorative material that is excellent in compression recovery property when foamed at a high magnification and that does not impair the design properties by embossing. The compression recovery property and embossing reproducibility of the foamed cosmetic material using the thermally expandable microcapsule foaming agent greatly depend on the shell film thickness of the thermally expandable microcapsule foaming agent after foaming. The thicker the shell film, the higher the ability to confine the encapsulated gas inside the shell, and the better the compression recovery. The thinner the gas, the easier the escape of the encapsulated gas, and the more likely the compression recoverability tends to be inferior. Further, the thicker the shell film, the easier it is to be repelled during embossing, so the embossing reproducibility is inferior. The thinner the embossing is, the better the embossing reproducibility tends to be. For this reason, it has been difficult to simultaneously impart both compression recovery and emboss reproducibility. Therefore, as a result of the thoughts and errors of the present inventors, mixing the thermally expandable microcapsule foaming agent with a thick shell film and the thermally expandable microcapsule foaming agent with a thin shell film makes it possible to improve compression recovery and emboss reproducibility. Succeeded in producing a foamed cosmetic material excellent in both. By mixing two types of thermally expandable microcapsule foaming agents with different shell film thickness, the thermally expandable microcapsule foaming agent with a thick shell film gives excellent compression recovery and the thermal expansion with a thin shell film thickness. This is because the microcapsule foaming agent imparts excellent emboss reproducibility.

According to a second aspect of the present invention, there is a total of 2 to 2 of the thermally expandable microcapsule foaming agent a and the thermally expandable microcapsule foaming agent b with respect to 100 parts by weight of the aqueous emulsion resin. The foamed decorative material according to claim 1, comprising 30 parts by weight and 20 to 200 parts by weight of the inorganic filler. By containing 2 to 30 parts by weight of the total of the thermally expandable microcapsule foaming agent a and the thermally expandable microcapsule foaming agent b and 20 to 200 parts by weight of the inorganic filler, high foaming and high performance such as strength can be achieved. It becomes possible to provide an excellent foamed decorative material. When the total of the thermally expandable microcapsule foaming agents a and b is less than 2 parts by weight, the foamability tends to decrease, and when it exceeds 30 parts by weight, the mechanical strength tends to decrease. Absent. Further, when the inorganic filler is less than 20 parts by weight, the flame retardancy tends to decrease, and when it exceeds 200 parts by weight, the foamability, mechanical strength, and crack resistance tend to decrease. Absent.

The content ratio a / b between the thermally expandable microcapsule foaming agent a and the thermally expandable microcapsule foaming agent b in claim 3 is 8/2 to 2/8. The foamed decorative material according to any one of the above. Excellent content of compression recovery when foamed at a high magnification because the content ratio a / b of the thermally expandable microcapsule foaming agent a and the thermally expandable microcapsule foaming agent b is 8/2 to 2/8. In addition, it is possible to provide a foamed decorative material in which the design by embossing is not impaired. If the ratio of the heat-expandable microcapsule foaming agent a exceeds a / b = 8/2, the compression recovery property tends to decrease. Therefore, it is not preferable.

The invention according to claim 4 is a surface of a foamed cosmetic material obtained by heating and foaming a resin composition containing at least the aqueous emulsion resin according to claim 1 , a thermally expandable microcapsule foaming agent, and an inorganic filler. Further, it is a foamed decorative material formed by pressing an embossed plate to form an uneven pattern . By applying embossing, it is possible to provide a foamed decorative material having a concavo-convex pattern and design characteristics.

  An example of the decorative material of the present invention will be described. FIG. 1 shows an example of the layer structure of the foamed decorative material of the present invention. As an example of the foamed decorative material of the present invention, as shown in FIG. 1, thermally expandable microcapsule foaming agents 22 and 23 and an inorganic filler 24 are aqueous emulsions on the surface of an appropriate base material 1 serving as a support. A foamed resin layer 2 made of a resin composition mixed and dispersed in a resin 21 is provided. Moreover, the said foamed resin layer may be comprised from the multilayer of 2 or more layers as needed.

  The base material 1 is a base material for the decorative material of the present invention, and the material is not particularly limited. For example, paper, woven fabric, non-woven fabric, etc. are moisture permeable and preferably in a flexible sheet state. Anything is ok. In the case of wallpaper, so-called wallpaper backing paper can be suitably used.

The foamed resin layer 2 is provided on the substrate 1 and is configured by mixing and dispersing thermally expandable microcapsule foaming agents 22 and 23 and an inorganic filler 24 in an aqueous emulsion resin 21. Colorants, dispersants, antiblocking agents, antifoaming agents, thickeners, UV absorbers, light stabilizers, antioxidants, matting agents, lubricants, antifriction agents, antistatic agents, antibacterials as necessary Various additives such as agents and fungicides may be added.
Further, the foamed resin layer may have a multilayer structure of two or more layers as necessary, and at this time, the composition of the resin composition may be changed depending on the layer.

The aqueous emulsion resin 21 is preferably a thermoplastic synthetic resin. Specific examples of the thermoplastic synthetic resin include, for example, vinyl acetate resin, ethylene-vinyl ester copolymer, acrylic resin, ethylene- (meth) acrylic ester copolymer, polyurethane resin, and polyester resin. , Epoxy resins, silicone resins, polybutene resins, polybutadiene resins, styrene-butadiene copolymers, etc., and these two or more types of copolymers or mixtures are contained as active ingredients. Also good.

  Examples of the polymerizable monomer used for the thermally expandable microcapsule blowing agents 22 and 23 include acrylonitrile, methacrylonitrile, α-chloroacrylonitrile, α-ethoxyacrylonitrile, fumaronitrile, acrylic acid, methacrylic acid, itaconic acid, maleic acid, Fumaric acid, citraconic acid, vinylidene chloride, vinyl acetate, methyl (meth) acrylate, ethyl (meth) acrylate, n-butyl (meth) acrylate, isobutyl (meth) acrylate, t-butyl (meth) acrylate, isobornyl (meta ) (Meth) acrylate such as acrylate, cyclohexyl (meth) acrylate, benzyl (meth) acrylate, β-carboxyethyl acrylate, styrene, α-methylstyrene, chlorostyrene, etc. Emissions monomers, acrylamide, substituted acrylamides, methacrylamides, substituted methacrylamides, butadiene and the like. These polymerizable monomers can be used alone or in combination of two or more. The combination can be selected according to all uses such as the softening temperature, heat resistance, and chemical resistance of the polymer. For example, a copolymer containing vinylidene chloride and a copolymer containing a nitrile monomer are excellent in gas barrier properties, and as shown in Japanese Patent No. 2131557, a copolymer containing 80% by weight or more of a nitrile monomer. The polymer is excellent in heat resistance and chemical resistance.

A cross-linking agent can be added as necessary. Examples include divinylbenzene, ethylene glycol dimethacrylate, triethylene glycol dimethacrylate, triacryl formal, trimethylolpropane trimethacrylate, allyl methacrylate, 1,3-butyl glycol dimethacrylate, triallyl isocyanate, and the like. However, it is not limited to these.

The shell of the thermally expandable microcapsule foaming agent (outer wall of the foaming agent) is adjusted by appropriately blending the above components with a polymerization initiator. Known polymerization initiators such as peroxides and azo compounds can be used as the polymerization initiator. Examples include azobisisobutyronitrile, benzoyl peroxide, lauryl peroxide, diisopropyl peroxydicarbonate, t-butyl peroxide, 2,2′-azobis (2,4-dimethylvaleronitrile), and the like. It is not limited to these. Preferably, an oil-soluble polymerization initiator soluble in the polymerizable monomer to be used is used.

The encapsulated gas included in the thermally expandable microcapsule foaming agent is a substance that becomes gaseous at or below the softening point of the shell, and known materials are used. Examples thereof include low boiling point liquids such as propane, propylene, butene, normal butane, isobutane, isopentane, neopentane, normal pentane, cyclopentane, hexane, heptane, petroleum ether, octane, isooctane and decane. Preferably, low-boiling-point liquids such as isobutane, normal butane, normal pentane, isopentane, cyclopentane, and petroleum ether are used alone or in admixture of two or more.

The heat-expandable microcapsule foaming agent used in the present invention has an average particle diameter of 5 to 35 μm, an encapsulated gas amount of 10 to 35%, and a shell film thickness at the time of maximum foaming of 0.03 to 0.10 μm. Thermally expandable microcapsule foaming agent a22 which is a thermally expandable hollow sphere, the average particle diameter of the original granules is 5 to 35 μm, the amount of encapsulated gas is 10 to 35%, and the shell film thickness at the time of maximum foaming is 0.10 to 0 A 25 μm thermally expandable hollow sphere, which is a thermally expandable microcapsule foaming agent b23, is mixed and used.

A foaming agent having an average particle size of less than 5 μm is not preferred because the shell layer after foaming becomes thin and the compression recovery property tends to be poor. Those having an average particle diameter of 35 μm or more are not preferable because the surface properties of the foamed decorative material tend to be inferior. Further, if the amount of encapsulated gas is less than 10%, the expansion ratio of the foaming agent tends to be small and embossing tends to be unfavorable, and if it is 35% or more, the foaming agent expands too much to form a shell layer after foaming. It is not preferable because it becomes thinner and the compression recovery property is lowered.

In addition, when the foamed shell film thickness is 0.03 μm or less, the compression recovery property of the wallpaper tends to be lowered, and when the foamed shell film thickness is 0.25 μm or more, the wallpaper is embossed. It is not preferable because the tendency is inferior. Thermally expandable microcapsule foaming agent a which is a thermally expandable hollow sphere having a shell film thickness of 0.03 to 0.10 μm at the time of maximum foaming and thermal expansion of a shell film thickness of 0.10 to 0.25 μm at the time of maximum foaming A foamed cosmetic material that is excellent in compression recovery when foamed at a high magnification and does not impair the design by embossing by mixing with the thermally expandable microcapsule foaming agent b, which is a porous hollow sphere It becomes possible to do. The compression recovery property and embossing reproducibility of the foamed cosmetic material using the thermally expandable microcapsule foaming agent greatly depend on the shell film thickness of the thermally expandable microcapsule foaming agent after foaming. The thicker the shell film, the higher the ability to confine the encapsulated gas inside the shell, and the better the compression recovery. The thinner the gas, the easier the escape of the encapsulated gas, and the more likely the compression recoverability tends to be inferior. Further, the thicker the shell film, the easier it is to be repelled during embossing, so the embossing reproducibility is inferior. The thinner the embossing is, the better the embossing reproducibility tends to be. For this reason, it has been difficult to simultaneously impart both compression recovery and emboss reproducibility.
Therefore, as a result of the thoughts and errors of the present inventors, mixing the thermally expandable microcapsule foaming agent with a thick shell film and the thermally expandable microcapsule foaming agent with a thin shell film makes it possible to improve compression recovery and emboss reproducibility. Succeeded in producing a foamed cosmetic material excellent in both. By mixing two types of thermally expandable microcapsule foaming agents with different shell film thickness, the thermally expandable microcapsule foaming agent with a thick shell film gives excellent compression recovery and the thermal expansion with a thin shell film thickness. This is because the microcapsule foaming agent imparts excellent emboss reproducibility.

Here, the primary particle means a thermally expandable microcapsule foaming agent before foaming, and the average particle size of this primary particle can be measured with a Nikkiso Microtrac particle size analyzer. In addition, the measurement of the amount of encapsulated gas in the original granules is defined as the amount of encapsulated material (%) obtained by adding an organic solvent to the foaming agent to swell the outer wall of the sphere, destroying it at high temperature, and subtracting moisture from this volatile component.

In addition, the shell film thickness at the time of maximum foaming is an aqueous emulsion containing an ethylene vinyl acetate copolymer having a heat flow midpoint of 130 ° C. to 150 ° C. and a toluene insoluble content of 15% or less among the aqueous emulsion (A), and It measures using the aqueous | water-based emulsion (A ') whose ethylene content in a copolymer is 15-20%. As a measurement method, an aqueous emulsion (A ′), calcium carbonate, and thermally expandable hollow spheres are blended in a dry ratio to an aqueous emulsion (A ′): calcium carbonate: thermally expandable microcapsule foaming agent = 100: 80: 10, When foaming is performed at 180 ° C. for 30 seconds, which is a predetermined foaming condition, the maximum foaming is set. The shell layer thickness at the time of maximum foaming was mathematically calculated from the thickness of the shell of the original grain before foaming by the foaming ratio at the time of maximum foaming as shown below. The shell thickness of the original grains was measured by observing the cross section of the original grains with a laser microscope.

(Calculation method of shell film thickness)
First, the specific gravity d ₂ of the thermally expandable microcapsule foaming agent particles after foaming is determined.
d ₂ = (weight after foaming of foamed cosmetic material to which thermally expandable microcapsule foaming agent is added−weight of foamed cosmetic material to which thermally expandable microcapsule foaming agent is not added) / (thermally expandable microcapsule foaming agent) The volume after foaming of the foamed cosmetic material to which is added-the volume of the foamed cosmetic material to which no thermally expandable microcapsule foaming agent is added.
Next, the radius r ₂ , volume V ₂ and weight W ₂ of the particles after foaming are determined.
It is calculated by r ₂ = r ₁ × (d ₁ / d ₂ ) ^(1/3) .
Here, r ₁ is the radius of the particles before foaming, and d ₁ is the specific gravity of the particles before foaming.
Calculated by V ₂ = 4/3 × π × r ₂ ³
Calculated as W ₂ = d ₂ × V ₂ .
Then, the weight W ₃ and volume V ₃ of the shell after foaming are obtained.
Calculated as W ₃ = W ₂ −W ₂ × Y / 100.
Here, Y is the amount of inclusion (%).
Calculated as V ₃ = W ₃ / d ₃ .
Here, d ₃ is the specific gravity of the shell.
Further, the radius r ₄ of the encapsulated gas filling part in the particles after foaming is obtained.
r ₄ = (r ₂ ³ −3 × V ₃ / 4π) ^(1/3) .
Then, the radius of the shell after foaming, that is, the shell film thickness r ₃ is obtained.
r ₃ = r ₂ −r ₄ = r ₁ × (d ₁ / d ₂ ) ^(1/3) − (r ₂ ³ −3 × V ₃ / 4π) ^(1/3) .
The above is the calculation method of the shell film thickness.

The total content of the thermally expandable microcapsule foaming agents a and b in the composition of the present invention is usually 2 to 30 parts by weight, preferably 5 to 15 parts by weight per 100 parts by weight (solid content) of the aqueous emulsion resin. Part. When the thermally expandable microcapsule foaming agent is less than 2 parts by weight, the foamability tends to be insufficient, and when it is more than 30 parts by weight, the mechanical strength tends to decrease, such being undesirable.

The ratio of the contents of the thermally expandable microcapsule foaming agents a and b is as follows: thermal expandable microcapsule foaming agent a / thermally expandable microcapsule foaming agent b = 8/2 to 2/8, preferably 6/4 to 4/6. If the ratio of the thermally expandable microcapsule foaming agent a exceeds a / b = 8/2, the compression recovery property tends to be unfavorable, and if it is less than a / b = 2/8, the design properties due to embossing tend to be inferior. So it is not preferable.

Examples of the inorganic filler 24 include aluminum hydroxide, magnesium hydroxide, barium hydroxide, calcium carbonate, magnesium carbonate, calcium sulfate, barium sulfate, ferrous hydroxide, basic zinc carbonate, basic lead carbonate, silica sand, clay , Talc, silicas, titanium dioxide, magnesium silicate and the like. Among these, aluminum hydroxide, magnesium hydroxide, calcium carbonate, and magnesium carbonate are preferable.

The content of the inorganic filler 24 in the resin composition is usually 20 to 200 parts by weight, preferably 50 to 150 parts by weight, per 100 parts by weight (solid content) of the aqueous emulsion resin. In the case of 20 parts by weight or less, the flame retardancy tends to be lowered, and in the case of 200 parts by weight or more, it tends to be inferior in foamability, mechanical strength, and crack resistance, which is not preferable.

Hereinafter, an example of the cosmetic material manufacturing method of the present invention will be described.

First, the resin composition which comprises the foamed resin layer 2 is mix | blended. At this time, the total content of the thermally expandable microcapsule foaming agents 22 and 23 is preferably 2 to 30 parts by weight per 100 parts by weight (solid content) of the aqueous emulsion resin.

Next, the blended resin composition is applied onto the substrate 1 to form the foamed resin layer 21. Examples of the coating method for the resin composition include coating methods such as knife coating, nozzle coating, die coating, lip coating, comma coating, gravure coating, rotary screen coating, and reverse roll coating. It is done.

When the layer constituting the foamed resin layer 2 is composed of two or more layers, it may be formed by coating one layer at a time from the lower layer to the upper layer, or all layers may be formed using a multilayer coating device. The coating may be formed at the same time. In the former case, the lower layer may be formed by drying and solidifying the lower layer, but the upper layer may be applied in a wet state without drying the lower layer. When formed, the respective layers are compatible with each other and have excellent interlayer adhesion.

The thickness of each layer constituting the foamed resin layer 2 is not particularly limited, and may be appropriately determined according to the intended use and required characteristics. For example, when used as wallpaper, the coating amount of the foamed resin layer 2 after drying is preferably about 50 to 300 g / m ² , more preferably about 100 to 250 g / m ² .

Next, the foamed resin layer 2 coated on the substrate 1 is dried. As a drying method after application of the foamable resin composition, for example, one kind selected from various conventionally known drying methods such as a hot air drying method, an infrared irradiation drying method, a vacuum drying method or the like, or a combination of two or more kinds is used. Can be used.

The drying temperature needs to be in a range not exceeding the foaming start temperature of the foamable resin composition. In particular, when the foamed resin composition has an aqueous emulsion resin as a main component, it is most preferably in the range of 90 to 95 ° C. not exceeding the boiling point of water. At this time, the foamed resin layer 2 may be gelled.

Next, the pattern 3 is printed on the foamed resin layer 2 as necessary. An appropriate pattern 3 may be printed and formed on the surface of the foamed resin layer 2 by using, for example, a gravure printing method, an offset printing method, a screen printing method, or the like.

As a heating method for foaming the foamed resin layer 2, a hot air heating method, an infrared heating method, or a combination thereof can be used. The heating temperature and the heating time are determined by the melt viscosity characteristics of the aqueous emulsion resin that is the main component of the resin composition constituting the foamed resin layer 2 and the foaming temperature characteristics of the foaming agent added to the resin composition. For example, general conditions when using a resin composition in which a thermally expandable microcapsule foaming agent is added to an aqueous emulsion resin are a heating temperature of 140 to 200 ° C. and a heating time of 20 to 80 seconds.

Further, the uneven pattern 4 may be formed on the surface of the foamed resin layer 2. Examples of the forming method include a mechanical embossing method in which an embossed plate is pressed against the surface of the foamed resin layer 2 after heating and foaming.

Examples of the present invention will be specifically described below. The present invention is not limited to these examples.

<Examples 1-3>
Table 1 shows the average particle diameter of the thermally expandable microcapsule foaming agent, the shell film thickness of the original granules, the amount of encapsulated gas, the maximum expansion ratio, and the shell film thickness at the time of maximum expansion.

^On a general paper substrate having a basis weight of 100 g / m ^2, the resin composition shown in the examples in Table 2 below is applied to a basis weight (coating amount after drying) of 150 g / m ² to obtain a foamed resin layer. 2 was formed. Subsequently, drying was performed in a drying furnace at a drying temperature of 90 ° C. for 1 minute. Further, a pattern 3 was printed on the foamed resin layer 2 by gravure printing using water-based ink. Finally, foaming was performed in a foaming furnace at a heating temperature of 180 ° C. for 30 seconds, and embossing was performed by a mechanical embossing method to form a concavo-convex pattern 4. From the above, a foamed decorative material could be obtained.

<Comparative Examples 1-4>
The foamed decorative materials of Comparative Examples 1 to 4 were prepared in the same manner as in the Examples by changing the resin composition as described in Table 2.

  About the foaming decorative material obtained in Examples 1-3 and Comparative Examples 1-4, foaming magnification, compression recovery property, and embossing property were evaluated by the method to be described later. The results are shown in Table 2.

(Foaming ratio)
The thickness (a) of the dried foamed resin layer before foaming was measured and used as the initial value. Next, the foamed resin layer thickness (b) of the foamed decorative material after foaming in the foaming furnace was measured, and (b) / (a) was calculated as the foaming ratio.

(Compression recovery rate)
The produced foamed decorative material was cut into a size of 2 cm × 2 cm, the thickness (c) of the test piece before compression was measured, and this was taken as the initial value. Next, 1000 g of weight was placed on the test piece and compressed at a pressure of 250 g / cm ² . After standing for 24 hours, the weight was removed and the pressure was released. After standing for another 24 hours, the thickness (d) of the test piece was measured, and (d) × 100 / (c) was calculated as the compression recovery rate.

(Embossing)
Mechanical embossing was carried out on the produced foamed decorative material, and evaluation was given as ○ when the reproducibility of the pattern of the embossed plate was particularly good, Δ when it was good, and × when the reproducibility of the embossed plate was poor.

Table 2 shows the resin composition and evaluation results of the foamed decorative material of the present invention.

As explained in detail above, the foamed cosmetic material of the present invention maintains excellent compression recovery even when foamed at a high magnification, the weight of the product itself at the time of storage, or a dent due to roller pressing during construction or after construction The present invention relates to a foamed decorative material that is recoverable against crushing caused by placement marks and that does not impair the design properties of embossing, and is useful as an interior material for buildings.

It is a schematic cross section which shows embodiment of the decorative material of this invention.

Explanation of symbols

1 Base material
2 Foamed resin layer 21 Aqueous emulsion resin 22 Thermally expandable microcapsule foaming agent a
23 Thermally expandable microcapsule foaming agent b
24 Inorganic filler 3 Pattern printing layer 4 Embossed uneven pattern

Claims (4)

A foaming cosmetic material obtained by heating and foaming a resin composition containing at least an aqueous emulsion resin, a thermally expandable microcapsule foaming agent, and an inorganic filler, wherein the thermally expandable microcapsule foaming agent is a thermally expandable microcapsule. Consists of two types of capsule foaming agent a and thermally expandable microcapsule foaming agent b,
The heat-expandable microcapsule foaming agent a has an average particle diameter of 5 to 35 μm, an included gas amount of 10 to 35%, and a shell film thickness at the time of maximum foaming of 0.03 to 0.10 μm.
The heat-expandable microcapsule foaming agent b has an average particle diameter of 5 to 35 μm, an amount of encapsulated gas of 10 to 35%, and a shell film thickness at the time of maximum foaming of 0.10 to 0.25 μm.
A foamed decorative material characterized by that. The total amount of the thermally expandable microcapsule foaming agent a and the thermally expandable microcapsule foaming agent b is 2 to 30 parts by weight with respect to 100 parts by weight of the aqueous emulsion resin, and the inorganic filler is 20 parts by weight. The foamed decorative material according to claim 1, further comprising -200 parts by weight. The content ratio a / b between the thermally expandable microcapsule foaming agent a and the thermally expandable microcapsule foaming agent b is 8/2 to 2/8. The foamed cosmetic material described. An embossed plate is pressed against the surface of a foamed decorative material obtained by heating and foaming a resin composition containing at least the aqueous emulsion resin according to claim 1 , a thermally expandable microcapsule foaming agent, and an inorganic filler. A foamed decorative material characterized by forming a pattern .

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