JP4816312B2 - Face pack - Google Patents

Description

  The present invention relates to a non-woven fabric for skin application and a face pack which are excellent in adhesion at the time of skin application and excellent in liquid retention properties such as lotion and cosmetic liquid.

  In recent years, various sheet-like face packs have been provided for portability and ease of use. In any of these, a sheet base material such as a nonwoven fabric or paper is impregnated with a skin lotion or cosmetic liquid having a whitening effect or a moisturizing effect, and is applied for a long time.

  However, a 100% cotton non-woven fabric or 100% rayon non-woven fabric, which is impregnated with lotion or cosmetic liquid, has low adhesion to the curved surface and unevenness of the face, so it may fall off during application. The chemical ingredients were not sufficiently permeable to the skin. Therefore, in order to improve the adhesion to various curved surfaces, methods have been adopted in which the surface of the nonwoven fabric is made uneven or imparted with a mesh shape to give stretchability, but it has not had sufficient adhesion. In addition, a method is disclosed in which a base material containing a cosmetic liquid or a cosmetic liquid is used to increase the adhesiveness by using a high-viscosity material or a water-containing gel (for example, Patent Document 1 and Patent Document 2). When the adhesive is made sticky, the adhesion at the time of skin application is improved, but there is a problem that the sheet base materials adhere to each other when the sheet base materials are spread before the skin application, and the handleability is poor.

In addition, face packs need to have a long-lasting effect depending on the purpose of use, but conventional 100% cotton non-woven fabrics and 100% rayon non-woven fabrics contain lotions and beauty that contain active ingredients from the layer opposite the application surface. Due to the rapid evaporation of the liquid, the sustainability of the effect was short, and it could not be said that the practicality was sufficient.
JP 2000-143484 A JP 2001-104468 A

  In view of the background of such prior art, the present invention provides a non-woven fabric for skin application and a face pack that are more excellent in adhesion and excellent in liquid retention properties such as lotion or cosmetic liquid when used for a long time. Is.

  The inventors of the present invention considered that the conventional non-woven fabric for skin application using cotton or rayon was not sufficiently thin in the single fiber diameter, and as a result of intensive studies, the present inventors arrived at the present invention.

That is, the present invention is a laminated nonwoven fabric formed by laminating and integrating at least two layers of nonwoven fabric, wherein the laminated nonwoven fabric is made of (A) a nanofiber made of a thermoplastic resin having a number average single fiber diameter of 1 to 500 nm. A non-woven fabric layer composed of fibers and (B) a non-woven fabric layer composed of fibers having a number average single fiber diameter of 1 to 100 μm larger than that of the nanofiber, and the layer (A) is affixed A face pack, wherein a non-woven fabric for skin application used as a surface is impregnated with skin lotion or cosmetic liquid.

  According to the present invention, by using a nanofiber having a remarkably small single fiber diameter on a pasting surface compared to a conventional material, a fiber having very excellent adhesion and a single fiber diameter larger than that of the nanofiber. By laminating layers, it is possible to provide a non-woven fabric for skin application and a face pack excellent in liquid retention.

  The nonwoven fabric for skin application of this invention has the nonwoven fabric layer comprised by the nanofiber which consists of (A) thermoplastic resin. As the thermoplastic resin, polyester, polyamide, polyolefin, or the like can be used. Other components may be copolymerized with these thermoplastic resins. Moreover, you may contain additives, such as a stabilizer.

  The nanofiber referred to in the present invention refers to a fiber having a number average single fiber diameter of 1 to 500 nm.

  By using the nanofibers defined in this range, the fibers enter the fine grooves on the skin surface and the adhesion is greatly improved. In addition, it has nano-order voids between the fibers, so that the liquid absorbency and liquid retention of skin lotion and cosmetic liquid are greatly improved.

  The single fiber diameter based on the number average of such nanofibers is preferably 1 to 200 nm, more preferably 50 to 150 nm.

  In addition, the nanofiber in the present invention is in the form of a single fiber dispersed separately, a single fiber partially bonded, an aggregate of a plurality of single fibers (for example, a bundle), etc. That is, what is necessary is just a so-called fibrous form, and it does not stick to its length or cross-sectional shape.

  Here, as a method for obtaining the nanofiber, for example, the following method can be employed.

  That is, from two or more types of polymers having different solubility in solvents, a polymer alloy melt is formed in which the easily soluble polymer is the sea (matrix) and the hardly soluble polymer is the island (domain). After spinning this, it is cooled and solidified. And fiberize. And after extending | stretching and heat processing as needed and obtaining a polymer alloy fiber, it is set as a fabric (nonwoven fabric) by a conventional method. Then, nanofibers can be obtained by removing the easily soluble polymer with a solvent.

  In this method, since the diameter of the nanofiber is almost determined by the size of the island (domain) in the polymer alloy fiber that is the precursor of the nanofiber, it is important to control the size of the island (domain) in the polymer alloy fiber. is there.

  The island (domain) size can be controlled by controlling the kneading of the polymer and is preferably highly kneaded by a kneading extruder, a stationary kneader or the like. In a simple chip blend (for example, JP-A-10-53967), kneading is insufficient, and it is difficult to disperse islands with a size of several tens of nm.

In addition, a combination of polymers is also important for ultra-fine dispersion of islands with a size of several tens of nanometers. In order to make an island (domain) close to a circle, the island (domain) polymer and the sea (matrix) polymer are preferably incompatible with each other. However, it is difficult to sufficiently ultra-disperse the island (domain) polymer by a simple combination of incompatible polymers. Therefore, a combination of polymers may be selected using the solubility parameter (SP value) as an index. Here, the SP value is a parameter reflecting the cohesive strength of a substance defined by (evaporation energy / molar volume) ^1/2 , and the SP value of various polymers is, for example, “Plastic Data Book” Asahi Kasei Amidus Co., Ltd. / Plastic editorial co-editor, page 189, etc.

It is preferable that the difference in SP value between the two polymers is 1 to 9 (MJ / m ³ ) ^{1/2 because} it is easy to achieve both circularization of islands (domains) due to incompatibility and ultrafine dispersion. For example, the difference in SP value between nylon 6 (N6) and polyethylene terephthalate (PET) is about 6 (MJ / m ³ ) ^1/2, which is a preferable example, but N6 and polyethylene (PE) have an SP value. The difference is about 11 (MJ / m ³ ) ^1/2, which is an undesirable example.

  In addition, the melt viscosity is also important. If the melt viscosity of the polymer forming the island component is set lower than that of the sea component, the island component polymer is likely to be deformed by shearing force, so that the island component polymer can be finely dispersed. It is preferable from the viewpoint of easy formation of nanofibers. However, if the island component polymer is excessively low in viscosity, it tends to be seamed and the blend ratio with respect to the entire fiber cannot be increased. Therefore, the viscosity of the island component polymer is preferably 1/10 or more of the viscosity of the sea component polymer.

  Examples of the solvent that dissolves the sea (matrix) polymer and hardly dissolves the island (domain) polymer include an alkaline solution, an acidic solution, an organic solvent, and a supercritical fluid. For example, in a combination of nylon and polyester, nylon exhibits poor solubility and polyester exhibits easy solubility in an alkaline solution.

  The nonwoven fabric for skin application of the present invention is composed of fibers having a number average single fiber diameter larger than that of the nanofibers in addition to the nonwoven fabric layer ((A) layer) composed of nanofibers as described above. It is important to have a non-woven fabric layer ((B) layer) that is laminated.

  By laminating the layers (B), effects that cannot be obtained with nanofibers alone can be expressed. For example, a non-woven fabric layer (layer (A)) composed of nanofibers alone cannot withstand actual use due to its weak strength, but by laminating layer (B), while taking advantage of the nanofiber adhesion effect, etc. The mechanical strength of the fiber structure can be improved, and a reinforcing effect can be obtained.

  In addition, the nonwoven fabric layer ((A) layer) composed of nanofibers alone may cause a dimensional change due to water absorption swelling when subjected to higher-order processing, but the (B) layer is laminated. Thus, dimensional stability can be imparted.

  In addition, if the nanofiber is simply mixed with other fibers having a large single fiber diameter, the adhesion of the nanofiber to the skin as described above is impaired. However, by adopting a laminated structure of the (A) layer and the (B) layer, the above effects can be obtained without impairing the adhesion to the skin.

Number monofilament diameter by the average of the fibers constituting the layer (B), in terms of the effects described above, it is 1 to 100 [mu] m.

  Further, the fibers constituting the layer (B) may be a mixture of two or more kinds of fibers having different single fiber diameters.

  (B) The fiber which comprises a layer may blend 2 or more types from which a raw material differs.

  The method for forming the (A) layer and the (B) layer may be a dry method or a wet method.

  In addition, as a method of forming the laminated nonwoven fabric, a method of attaching a binder between the (A) layer and the (B) layer, a method of entanglement with a needle punch or high-pressure water flow, and a method of heating the (B) layer. A method in which fusible fibers are mixed and heat-sealed with a heating roll, and a fiber constituting the other layer (or a fiber of its precursor) is directly laminated on one layer by a melt blow method or a spun bond method. A method or the like can be adopted.

  Moreover, about (A) layer, a nonwoven fabric layer or a laminated nonwoven fabric may be formed in the state of the polymer alloy fiber which is a precursor of a nanofiber, and nanofiber may be formed by sea removal treatment after that.

  The proportion of the (A) layer in the laminated nonwoven fabric is preferably 15% by mass or more, more preferably 20% by mass or more, and further preferably 25% by mass or more. By setting it as 15 mass% or more, it can prevent that another fiber is exposed to the surface of a nanofiber layer from between the fibers of a nanofiber, and can prevent that adhesiveness is inhibited. Moreover, as an upper limit, it is preferable that it is 50 mass% or less. By setting it to 50% by mass or less, sufficient strength as a non-woven fabric for skin application can be obtained.

As a laminated structure in the laminated nonwoven fabric, it is sufficient that at least the affixing surface is composed of a nonwoven fabric layer ((A) layer) made of nanofibers, (A) layer / (B) layer / (A) layer, (A ) Layer / (B ₁ ) layer / (B ₂ ) layer, (A) layer / (B ₁ ) layer / (B ₂ ) layer / (A) layer, etc. can be employed. Here, the (B ₁ ) layer and the (B ₂ ) layer are (B) layers having different single fiber diameters and materials.

As a fabric weight of a laminated nonwoven fabric, 30-150 g / m < ² > is preferable, More preferably, it is 30-100 g / m < ² >. By setting the basis weight to 30 g / m ² or more, the form stability is good and the handleability during use is good. Moreover, by setting it as 150 g / m < ² > or less, even if it absorbs a chemical | medical solution, weight does not become heavy and it can prevent that adhesiveness worsens.

  The laminated nonwoven fabric preferably has an average tensile strength when wet of 0.5 N / 50 mm or more, more preferably 50 N / 50 mm or more, still more preferably 100 N / 50 mm or more, and even more preferably 300 N / 50 mm or more. It is. By setting the tensile strength at the time of wetting to 0.5 N / 50 mm or more, the process passability at the time of impregnation with a chemical solution can be satisfied.

  In addition, the laminated nonwoven fabric preferably has a tear-and-width average tear strength of 1 N or more, more preferably 5 N or more, and even more preferably 10 N or more. By setting it to 1N or more, it is possible to prevent a problem that a hole is torn during pasting. Moreover, although an upper limit is not specifically limited, 100N should just be sufficient.

  In the present invention, the vertical direction and the horizontal direction are defined as a direction parallel to the advancing direction of the laminating process and a direction orthogonal to the vertical direction.

  Moreover, it is preferable that the laminated nonwoven fabric has a water retention within a range of 300 to 2000%. A chemical | medical solution can fully be absorbed by water retention being 300% or more. Moreover, by setting it as 2000% or less, the weight as a face pack etc. which absorbed the chemical | medical solution does not become heavy too much, but the problem that it expands greatly and it is difficult to apply to a desired site | part can also be prevented.

The skin patch for nonwoven fabric in the present invention, Ru der that the nonwoven fabric used as the base material of the product for the purpose of affixing the human skin.

  In particular, the non-woven fabric for skin application of the present invention is excellent in adhesion to the skin and has high liquid retention, and thus can be suitably used as a base material for a face pack taking advantage of the above characteristics.

  The face pack as used herein is a beauty tool for performing skin care by applying a sheet impregnated with an appropriate amount of a lotion or cosmetic liquid containing an active ingredient having a cosmetic effect to the entire face or a part of the face. .

  As the skin lotion or cosmetic liquid, chemical liquid components generally used in pharmaceuticals, quasi drugs, cosmetics, hygiene materials, sundries, etc. can be applied. Examples of active ingredients with beauty effects include humectants such as sugars, amino acids, placenta extract, hyaluronic acid, glycerin, sorbitol, and polyethylene glycol, softeners such as olive oil, cetyl alcohol, lanolin, and stearyl alcohol, and vitamins Examples thereof include blood circulation promoters such as E, anti-inflammatory agents such as glycyl phosphate, and skin-beautifying components such as various vitamin Cs.

  Examples of the present invention will be specifically described below.

[Measuring method]
(1) Domain size in sea-island structure A synthetic fiber is sliced so that a cross section appears, and the cross section is observed with a transmission electron microscope (TEM). 50 were randomly selected, the cross-sectional area of each island was measured with image analysis software, and the domain size corresponding to the diameter in terms of a true circle was calculated as an average value from the area.

(2) Non-woven fabric cross-section observation by TEM Non-woven fabric is embedded with epoxy resin, ultra-thin sections are cut out in the cross-sectional direction, and the non-woven fabric cross-section is observed with a transmission electron microscope (TEM) (H-7100FA type manufactured by Hitachi, Ltd.). Observed.

(3) Single fiber diameter based on the number average of nanofibers A nanofiber layer is extracted from a cross-sectional photograph of a nonwoven fabric by TEM, and 30 nanofibers adjacent to each other in the same photograph using image processing software (WINROOF) 10 groups were extracted at random, the diameter of a total of 300 single fibers was measured, the simple average value was obtained, and the single fiber diameter was determined by the number average of nanofibers.

(4) (B) Single fiber diameter based on the number of fibers in the layer The fineness is measured based on JIS L 1015, and the fineness and the specific gravity of the material listed in the “Fiber Handbook (Japan Chemical Fibers Association)” etc. The single fiber diameter of the fiber was determined. When the fiber was a modified cross-section fiber, the cross section of the modified cross-section fiber was calculated by converting it into a circle having the same area.

(5) Weight per unit area Measured based on JIS L 1913: 1998 6.2.
Three 300 mm × 300 mm test pieces were collected from the sample using a steel ruler and a razor blade. The mass of the test piece in the standard state was measured, the mass per unit area was determined by the following formula, and the average value was calculated.
m _s = m / S
Here, m _s : mass per unit area (g / m ² )
m: average weight of the test piece (g)
S: Area (m ² ) of the test piece.

(6) Mass ratio The mass ratio of the (A) layer with respect to the laminated nonwoven fabric was determined by measuring the basis weight according to the above (5) for each layer and calculating by the following formula.
(A) layer of the mass ratio _{(%) = (m A1 +} m A2 + ...) / (m A1 + m A2 + ... + m B1 + m B2 ...) × 100
Here, m _An : basis weight of layer (A) before lamination (g / m ² )
m _Bn : basis weight of layer (B) before lamination (g / m ² )
n = 1, 2,.

(7) Tensile strength when wet Measured according to JIS L 1913: 1998 6.3.2.
Five test pieces each having a width of 50 mm and a length of 300 mm were collected in the vertical direction and the horizontal direction.
The test piece was immersed in water at 20 ° C. for 1 hour, taken out, and immediately attached to a constant speed extension type tensile tester for measurement.
A load was applied until the specimen was cut at a pulling speed of 100 mm / min at a gripping interval of 200 mm, the strength at the maximum load was measured, and the average value of 10 vertical and horizontal sheets was calculated.

(8) Tear strength when wet Measured based on the JIS L 1913: 1998 6.4.2 trapezoid method except that the wet treatment was the same as in (7) above.
Using a template, collect five 75 mm x 150 mm test pieces in the vertical and horizontal directions, and place an isosceles trapezoidal mark on the test piece at the position indicated in this rule. A 15 mm cut was made perpendicular to the side.
Immediately after immersing the test piece in water at 20 ° C. and taking it out, the gripping interval of the test piece is set to 25 mm, the trapezoidal short side is stretched, the long side is loosened, and the gripping tool of the tensile tester is along the mark Attached to.
The tensile speed was 100 mm / min, and the average value of the tear strength of 10 vertical and horizontal sheets was calculated.

(9) Water retention rate Measured according to JIS L 1906: 2000 Appendix 3.2.
Three test pieces of 10 cm × 10 cm were collected, and the mass was measured up to 1 mg.
The test piece was immersed in tap water for 15 minutes at room temperature, and the test piece was taken out of the water with tweezers and watered or dropped for 1 minute, and then its mass was measured to 1 mg.
The water retention rate was calculated by the following formula, and the average value was further obtained.
m = (m ₂ −m ₁ ) / m ₁ × 100
Where m: water retention rate (%)
m ₁ : Mass of test specimen in standard state (mg)
m ₂ : Mass (mg) after wetting the test piece and dripping or dropping water.

(10) Performance evaluation Female panels impregnated with 20 ml of lotion (Kose “Snow skin spirit”) in the nonwoven fabrics obtained in each of the examples and comparative examples are used for adhesion, moistness, moisture retention, and handling. An absolute evaluation of each person by 10 persons gave an evaluation with a maximum of 10 points, and the evaluation was performed according to the following criteria from the average points of 10 persons (rounded to the nearest decimal place).
A: 9 to 10 points B: 7 to 8 points C: 5 to 6 points D: 3 to 4 points E: 0 to 2 points.

[Example 1]
(Polymer alloy fiber)
Melt viscosity 212 Pa · s (262 ° C., shear rate 121.6 sec ⁻¹ ), melting point 220 ° C. nylon 6 (N6) (40 mass%), weight average molecular weight 120,000, melt viscosity 30 Pa · s (240 ° C., shear Poly L-lactic acid (60 mass%) having a speed of 2432 sec ⁻¹ ) and a melting point of 170 ° C. and an optical purity of 99.5% or higher is separately weighed and separately supplied to a biaxial extrusion kneader having the following details. The polymer alloy chip was obtained by kneading.
Screw shape: Fully meshed in the same direction Double thread screw: Diameter 37 mm, effective length 1670 mm, L / D = 45.1
Kneading section length is 28% of screw effectiveness
The kneading part was positioned on the discharge side from 1/3 of the effective screw length.
There are 3 backflow parts on the way Vent: 2 places.

  The obtained polymer alloy chip is supplied to a uniaxial extrusion-type melting apparatus for a staple spinning machine, and melt spinning is performed at a melting temperature of 235 ° C., a spinning temperature of 235 ° C. (a base surface temperature of 220 ° C.), and a spinning speed of 1200 m / min. A polymer alloy fiber was obtained. After the yarns were combined, steam drawing was performed to obtain a tow made of polymer alloy fibers having a single yarn fineness of 3.0 dtex. The strength of the obtained polymer alloy fiber showed excellent properties of 3.5 cN / dtex, elongation of 45%, and U% = 1.0%. When the cross section of the fiber was observed with TEM, the islands (domains) had a number average diameter of 99 nm and were uniformly dispersed.

(Crimping and cutting process)
The tow made of the polymer alloy fiber was crimped (12 peaks / 25 mm) and then cut into 51 mm short fibers.

((A) non-woven fabric of layer)
After opening with the above short fiber card, a web was made with a cross-wrap weber. This web was needle punched at a punch density of 80 / cm ² to obtain a nonwoven fabric of layer (A) of 75 g / m ² .

((B) non-woven fabric of layer)
A cut fiber with a cut length of 51 mm made of nylon 6 (N6) / polybutylene terephthalate (PBT) composite fiber for split splitting (N6 fiber diameter after splitting, PBT fiber diameter after splitting of 7 μm) is opened with a card. After that, the web was made with a cross-wrap weber. This web was subjected to needle punching at a punch density of 80 / cm ² to obtain a nonwoven fabric of layer (B) having a basis weight of 70 g / m ² .

(Laminated nonwoven fabric)
The nonwoven fabric of layer (A) and the nonwoven fabric of layer (B) obtained above were laminated, and needle punching was performed at a punch density of 45 / cm ² to obtain a laminated nonwoven fabric having a basis weight of 145 g / m ² . .

(Nonwoven fabric for skin application)
By treating the laminated nonwoven fabric with a 1% aqueous sodium hydroxide solution at a temperature of 95 ° C. and a bath ratio of 1:40, polylactic acid is removed from the seawater, and N6 nanofibers and N6 / PBT split split yarns are used. A non-woven fabric for skin application having a basis weight of 100 g / m ² was obtained.

  The mass ratio of the nanofibers in the obtained non-woven fabric for skin application was 30%. From this, the nanofibers were extracted and observed with a TEM. As a result, the number average single fiber diameter was 99 nm. Moreover, this non-woven fabric for skin application was excellent in form stability.

[Example 2]
(Polymer alloy fiber)
Polymer alloy fibers similar to those used in Example 1 were used.

(Crimp / Cut configuration)
Using the polymer alloy fiber, the same crimping and cutting as in Example 1 was performed.

((A) non-woven fabric of layer)
A non-woven fabric of layer (A) was produced in the same manner as in Example 1 except that the basis weight was 45 g / m ² .

((B) non-woven fabric of layer)
A non-woven fabric of layer (B) was produced in the same manner as in Example 1 except that the basis weight was 42 g / m ² .

(Laminated nonwoven fabric)
The nonwoven fabric of layer (A) and the nonwoven fabric of layer (B) obtained above were laminated, and a laminated nonwoven fabric having a basis weight of 87 g / m ² was obtained in the same manner as in Example 1.

(Nonwoven fabric for skin application)
The laminated nonwoven fabric was subjected to sea removal treatment similar to that of Example 1 to obtain a nonwoven fabric for skin application having a basis weight of 60 g / m ² made of N6 nanofibers and N6 / PBT split split yarns.

  The mass ratio of the nanofibers in the obtained non-woven fabric for skin application was 30%. Moreover, this non-woven fabric for skin application was excellent in form stability.

[Example 3]
(Polymer alloy fiber)
Polymer alloy fibers similar to those used in Example 1 were used.

(Crimp / Cut configuration)
Using the polymer alloy fiber, the same crimping and cutting process as in Example 1 was performed to obtain a short fiber.

((A) non-woven fabric of layer)
A nonwoven fabric having a basis weight of 75 g / m ² was produced in the same manner as in Example 1 using the above short fibers.

((B) non-woven fabric of layer)
Cotton (American cotton having a micronaire fineness of 4.3, a fiber diameter of 12 μm, and an average fiber length of 1.1 × 2.54 cm) was opened with a card and then made into a web with a cross wrapper weber. This web was subjected to needle punching at a punch density of 80 / cm ² to obtain a nonwoven fabric of layer (B) having a basis weight of 70 g / m ² .

(Laminated nonwoven fabric)
The non-woven fabric of layer (A) and non-woven fabric of layer (B) obtained above were laminated, and a laminated non-woven fabric having a basis weight of 145 g / m ² was obtained in the same manner as in Example 1.

(Nonwoven fabric for skin application)
The laminated nonwoven fabric was subjected to sea removal treatment similar to that of Example 1 to obtain a nonwoven fabric for skin application having a basis weight of 100 g / m ² made of N6 nanofibers and cotton.

  The mass ratio of the nanofibers in the obtained non-woven fabric for skin application was 30%. Moreover, this non-woven fabric for skin application was excellent in form stability.

[Example 4]
(Polymer alloy fiber)
Polymer alloy fibers similar to those used in Example 1 were used.

(Crimping and cutting process)
Using the polymer alloy fiber, the same crimping and cutting process as in Example 1 was performed to obtain a short fiber.

((A) non-woven fabric of layer)
A non-woven fabric of layer (A) was produced in the same manner as in Example 1 except that the basis weight was 45 g / m ² .

((B) non-woven fabric of layer)
Cotton (American cotton having a micronaire fineness of 4.3, a single fiber diameter of 12 μm, and an average fiber length of 1.1 × 2.54 cm) was opened with a card and then made into a web with a cross wrapper weber. This web was subjected to needle punching at a punch density of 80 / cm ² to obtain a nonwoven fabric of layer (B) having a basis weight of 42 g / m ² .

(Laminated nonwoven fabric)
The nonwoven fabric of layer (A) and the nonwoven fabric of layer (B) obtained above were laminated, and a laminated nonwoven fabric having a basis weight of 87 g / m ² was obtained in the same manner as in Example 1.

(Nonwoven fabric for skin application)
The laminated nonwoven fabric was subjected to sea removal treatment similar to that of Example 1 to obtain a nonwoven fabric for skin application having a basis weight of 60 g / m ² made of N6 nanofibers and cotton.

  The mass ratio of the nanofibers in the obtained non-woven fabric for skin application was 30%. Moreover, this non-woven fabric for skin application was excellent in form stability.

[Example 5]
(Polymer alloy fiber)
The same polymer alloy fiber as used in Example 1 was used.

(Crimping and cutting process)
The tow made of the polymer alloy fiber was crimped (12 peaks / 25 mm) and then cut into 38 mm short fibers.

(Laminated nonwoven fabric)
After opening the short fiber with a card, a web for layer (A) was produced with a cross-wrap weber. Also, cotton (American cotton having a micronaire fineness of 4.3, a single fiber diameter of 12 μm, and an average fiber length of 1.1 × 2.54 cm) was opened with a card, and then a web for layer (B) was formed with a cross wrap webber. Produced. These webs are divided into 65 (g / m ² ) / 50 (g / m ² ) / 65 (g) of (A) layer web / (B) layer web / (A) layer web. / M ² ), and a water jet punch composed of a nozzle head having a hole diameter of 100 μm and a nozzle pitch of 0.6 mm is entangled at 10 MPa on both sides with a processing speed of 2.5 m / min. A laminated nonwoven fabric of 180 g / m ² was obtained.

(Nonwoven fabric for skin application)
The laminated nonwoven fabric was subjected to sea removal treatment similar to that of Example 1 to obtain a nonwoven fabric for skin application having a basis weight of 100 g / m ² made of N6 nanofibers and cotton.

  The nanofiber mass ratio of the obtained non-woven fabric for skin application was 49%. Moreover, this non-woven fabric for skin application was excellent in form stability.

[Comparative Example 1]
A face pack base material having a basis weight of 60 g / m ^{2 made} of a commercially available cotton nonwoven fabric was used.

  From the results in Table 1, it can be seen that Examples 1 to 5 have excellent characteristics as face packs. On the other hand, Comparative Example 1 had low adhesion, poor moisture retention, and poor handling during use.

Claims (8)

A laminated nonwoven fabric constituted by laminating and integrating at least two layers of nonwoven fabric, wherein the laminated nonwoven fabric is composed of nanofibers made of a thermoplastic resin having a single fiber diameter of 1 to 500 nm (A). Skin having at least a non-woven fabric layer and (B) a non-woven fabric layer composed of fibers having a single fiber diameter of 1 to 100 μm larger than the nanofiber, and using the layer (A) as a pasting surface A face pack, wherein a non-woven fabric for application is impregnated with a skin lotion or a cosmetic liquid.
The number single fiber diameter by the average of the nanofibers constituting the (A) layer is 200nm or less, face pack mounting serial to claim 1. The face pack according to claim 1 or 2 , wherein a proportion of the layer (A) in the laminated nonwoven fabric is 15% by mass or more. The face pack according to claim 3 , wherein a ratio of the layer (A) to the laminated nonwoven fabric is 50% by mass or less. The basis weight of the laminated nonwoven fabric is 30 to 150 g / ^{m 2,} a face pack according to any one of claims 1-4. The tension of the laminated nonwoven fabric of the wet strength is 50 N / 50 mm or more, a face pack according to any one of claims 1-5. The face pack according to any one of claims 1 to 5 , wherein the laminated nonwoven fabric has a tear strength of 1N or more when wet. The face pack according to any one of claims 1 to 7 , wherein a moisture retention of the laminated nonwoven fabric is 300 to 2000%.