PHOTO-CURING NAIL GEL COMPOSITION

Abstract

A photo-curing nail gel composition is provided, including a polyurethane (meth)acrylate resin (resin elongation rate: 200% to 700%), a diluent, a photo initiator, a surface curing accelerating agent and a filler. The diluent includes a monofunctional monomer, a difunctional monomer and a trifunctional monomer. The photo initiator performs the photo-initiation reaction of the composition. The surface curing accelerating agent includes a tertiary amine acrylic resin or a thiol resin. A content of the polyurethane (meth)acrylate resin is 50 wt % to 80 wt %, contents of the monofunctional monomer, the difunctional monomer and the trifunctional monomer are respectively 1 wt % to 30 wt %, a content of the photo initiator is 1 wt % to 10 wt %, a content of the surface curing accelerating agent is 1 wt % to 10 wt % and a content of the filler is 1 wt % to 10 wt %, based on a total weight of the photo-curing nail gel composition.

Claims

1. A photo-curing nail gel composition, comprising: a polyurethane (meth)acrylate resin, wherein a resin elongation rate of the polyurethane (meth)acrylate resin is 200% to 700%; a diluent, wherein the diluent includes a monofunctional monomer, a difunctional monomer and a trifunctional monomer; a photo initiator, which performs a photo-initiation reaction of the photo-curing nail gel composition; a surface curing accelerating agent, wherein the surface curing accelerating agent includes a tertiary amine acrylic resin or a thiol resin; and a filler, wherein a content of the polyurethane (meth)acrylate resin is 50 wt % to 80 wt %, contents of the monofunctional monomer, the difunctional monomer and the trifunctional monomer are respectively 1 wt % to 30 wt %, a content of the photo initiator is 1 wt % to 10 wt %, a content of the surface curing accelerating agent is 1 wt % to 10 wt % and a content of the filler is 1 wt % to 10 wt %, based on a total weight of the photo-curing nail gel composition.

2. The photo-curing nail gel composition of claim 1, further comprising a colorant, wherein a content of the colorant is 0.2 wt % to 3 wt %, based on a total weight of the photo-curing nail gel composition.

3. The photo-curing nail gel composition of claim 1, wherein the monofunctional monomer includes hydroxyethyl acrylate (HEA), hydroxyethyl methacrylate (HEMA), hydroxypropyl methacrylate (HPMA), acrylic acid (AA), methyl acrylic acid (MAA), isobornyl acrylate (IBOA) or isobornyl methacrylate (IBOMA).

4. The photo-curing nail gel composition of claim 1, wherein the difunctional monomer includes dipropylene glycol diacrylate (DPGDA), tripropylene glycol diacrylate (TPGDA), propoxylated neopentyl glycol diacrylate (NPG2PODA), 1,6-hexanediol diacrylate (HDDA), ethylene glycol dimethacrylate (EGDMA) or 2-hydroxylethyl methacrylate phosphate (HEMAP).

5. The photo-curing nail gel composition of claim 1, wherein the trifunctional monomer includes ethoxylated trimethylolpropane triacrylate (TMP3EOTA, TMP9EOTA and TMP15EOTA), propoxylated trimethylolpropane triacrylate (TMP3POTA) or propoxylated glyceryl triacrylate (G3POTA).

6. The photo-curing nail gel composition of claim 1, wherein the photo initiator includes diphenyl (2,4,6-trimethylbenzoyl)-phosphine oxide (TPO), ethyl(2,4,6-trimethylbenzoyl) phenylphosphinate (TPO-L), isopropyl thioxanthone (ITX) or camphorquinone (CQ).

7. The photo-curing nail gel composition of claim 1, wherein an absorption wavelength of the photo initiator is 320 nm to 400 nm.

8. The photo-curing nail gel composition of claim 1, wherein the filler includes methyl cellulose, carboxymethyl cellulose, nitrocellulose or acetyl cellulose.

9. The photo-curing nail gel composition of claim 1, wherein the photo-curing nail gel composition is cured under irradiation with a light source having a wavelength of 320 nm to 400 nm for 30 seconds.

Description

DESCRIPTION OF THE EMBODIMENTS

[0018] Reference will now be made in detail to the present preferred embodiments of the invention. However, these embodiments are illustrative examples, and the invention is not limited thereto.

[0019] It should be mentioned that in the specification and claims of the invention, “polyurethane (meth)acrylate resin” represents “polyurethane acrylate resin” and/or “polyurethane methacrylate resin”.

[0020] The invention provides a photo-curing nail gel composition including a polyurethane (meth)acrylate resin, a diluent, a photo initiator, a surface curing accelerating agent, a filler and a colorant. The mentioned components will be described in detail below.

<Polyurethane (Meth)Acrylate Resin>

[0021] A resin elongation rate of the polyurethane (meth)acrylate resin of the invention is 200% to 700%, which is the main toughness source of the colloid. Based on a total weight of the photo-curing nail gel composition, a content of the polyurethane (meth)acrylate resin is 50 wt % to 80 wt %, and preferably 50 wt % to 60 wt %. More specifically, the polyurethane (meth)acrylate resin of the invention may be obtained from commercially available products, such as: 6148-J75 produced by Eternal Materials Co., Ltd, CN966-J75 produced by Sartomer Co., DM553, DM5433H and DM5232 produced by Double Bond Chemical Inc., Co., Ltd. However, the invention is not limited thereto, and other commercially available products may also be used according to the actual operation condition.

<Diluent>

[0022] The diluent of the invention may include a monofunctional monomer, a difunctional monomer and a trifunctional monomer, which is mainly used to adjust formula viscosity and increase colloid crosslinking, so as to enhance curing rate, toughness and nail surface adhesion.

[0023] The monofunctional monomer may include hydroxyethyl acrylate (HEA), hydroxyethyl methacrylate (HEMA), hydroxypropyl methacrylate (HPMA), acrylic acid (AA), methyl acrylic acid (MAA), isobornyl acrylate (IBOA) or isobornyl methacrylate (IBOMA).

[0024] The difunctional monomer may include dipropylene glycol diacrylate (DPGDA), tripropylene glycol diacrylate (TPGDA), propoxylated neopentyl glycol diacrylate (NPG2PODA), 1,6-hexanediol diacrylate (HDDA), ethylene glycol dimethacrylate (EGDMA) or hydroxylethyl methacrylate phosphate (HEMAP).

[0025] The trifunctional monomer may include ethoxylated trimethylolpropane triacrylate (TMP3EOTA, TMP9EOTA and TMP15EOTA), propoxylated trimethylolpropane triacrylate (TMP3POTA) or propoxylated glyceryl triacrylate (G3POTA).

[0026] Based on the total weight of the photo-curing nail gel composition, contents of the monofunctional monomer, the difunctional monomer and the trifunctional monomer are respectively 1 wt % to 30 wt %. More specifically, when the contents of the difunctional monomer and the trifunctional monomer are respectively 1 wt % to 5 wt %, suitable reactivity and crosslinking can be achieved. When the content of the monofunctional monomer is 5 wt % to 10 wt % and the content of the difunctional monomer is 10 wt % to 15 wt %, the adhesion with nail can be enhanced. Besides, a total content of the monofunctional monomer, the difunctional monomer and the trifunctional monomer is less than 40 wt %.

[0027] However, if the contents of the difunctional monomer and the trifunctional monomer are higher than the upper limit of the aforementioned range, the reaction shrinkage rate may be too high. If the contents of the monofunctional monomer and the difunctional monomer are higher than the upper limit of the aforementioned range, it may be difficult to remove the gel by stripping procedure. If the contents of the monofunctional monomer and the difunctional monomer are lower than the upper limit of the aforementioned range, the adhesion may be worse. In addition, if the total content of the monofunctional monomer, the difunctional monomer and the trifunctional monomer is higher than 40 wt %, the curing effect is worse. Therefore, it is unable for the composition to cure and dry under irradiation with a light source having a wavelength of 320 nm to 400 nm for 30 seconds, and it is unable to remove the gel by stripping procedure.

<Photo Initiator>

[0028] The photo initiator of the invention performs a photo-initiation reaction of the photo-curing nail gel composition, and an absorption wavelength of the photo initiator is 320 nm to 400 nm. More specifically, the photo initiator may include diphenyl (2,4,6-trimethylbenzoyl)-phosphine oxide (TPO), ethyl(2,4,6-trimethylbenzoyl) phenylphosphinate (TPO-L), isopropyl thioxanthone (ITX) or camphorquinone (CQ). the photo initiator of the invention may be obtained from commercially available products, such as Irgacure® TPO, Irgacure® TPO-L, Irgacure®907, Irgacure®819 and Irgacure®369 produced by BASF Co. Based on the total weight of the photo-curing nail gel composition, the content of the photo initiator is 1 wt % to 10 wt %.

<Surface Curing Accelerating Agent>

[0029] The surface curing accelerating agent of the invention may include tertiary amine acrylic resin or thiol resin, and it is able to reduce the oxygen inhibition effect in the acrylic resin curing system, so as to further increase the colloid surface curing effect. Based on the total weight of the photo-curing nail gel composition, a content of the surface curing accelerating agent is 1 wt % to 10 wt %. More specifically, when the content of the surface curing accelerating agent is 1 wt % to 5 wt % and the content of the photo initiator is 1 wt % to 10 wt %, a better surface curing effect can be achieved.

[0030] The surface curing accelerating agent of the invention may include pentaerythritoltetrakis(3-mercaptobutyrate), trimethylolpropanetris(3-mercaptopropionate) or pentaerythritoltetrakis(3-mercaptopropionate). Besides, the surface curing accelerating agent of the invention may be obtained from commercially available products, such as: KarenzMT PE1 produced by Showa Denko Electronics Co., Ltd., 641, 6410, 6411, 6417 and 6430 produced by Eternal Materials Co., Ltd, DM L234 produced by Double Bond Chemical Inc., Co., Ltd, TMMP and PEMP produced by SC Organic Chemical Co., Ltd., ADDITOL™ LED 01 produced by Cytec Industries Inc. However, the invention is not limited thereto, and other commercially available products may also be used according to the actual operation condition.

<Filler>

[0031] The filler of the invention may include methyl cellulose, carboxymethyl cellulose, nitrocellulose or acetyl cellulose, wherein an esterification degree of acetyl cellulose is higher than 50%. Based on the total weight of the photo-curing nail gel composition, a content of the filler is 1 wt % to 10 wt %. More specifically, when the content of the filler is 2 wt % to 5 wt %, it is helpful to enhance the dispersing effect of pigment and surface curing effect.

<Colorant>

[0032] Based on the total weight of the photo-curing nail gel composition, a content of the colorant is 0.2 wt % to 3 wt %.

[0033] The following experimental examples will be used to describe the photo-curing nail gel composition of the invention. However, the following experimental examples are not intended to limit the invention.

EXPERIMENTAL EXAMPLE

[0034] The following experimental examples are used to prove that the photo-curing nail gel composition of the invention has properties of adhesion, beautification and scratch resistance, and it can be removed by stripping procedure.

Preparation of Photo-Curing Nail Gel Composition

[0035] The photo-curing nail gel compositions of Experimental Examples 1 to 4 and Comparative Examples a to f are prepared, wherein the content of each component are shown in the following Table 1 and Table 2. Experimental Examples 1 to 4 are photo-curing nail gel compositions of the invention.

[0036] In Table 2, the polyurethane (meth)acrylate resins used in Comparative Example e and f are respectively 6113 and 6127 produced by Eternal Materials Co., Ltd.

Evaluation 1: Curing and Drying Properties Evaluation After Light Irradiation

[0037] The photo-curing nail gel compositions of Experimental Examples 1 to 4 and Comparative Examples a to f and commercially available products A to D are applied on nails, and then irradiated with a LED light source having a wavelength of 320 nm to 400 nm for 30 seconds. Afterwards, curing and drying properties are evaluated. The evaluation results are shown in the following Table 1, Table 2 and Table 3, and the evaluation standards are as follows: [0038] Excellent ◯: Nearly no gel is left (<5%), which can be removed by alcohol wiping. [0039] Tolerable Δ: More gel is left (>5%), which can be removed by alcohol wiping. [0040] Poor x: It is totally unable to cure the composition.

Evaluation 2: Stripping Property Evaluation

[0041] After the photo-curing nail gel compositions of Experimental Examples 1 to 4 and Comparative Examples a to f and commercially available products A to D applied on nails are cured, try to strip off the cured composition or the cured commercially available products with fingers and observe whether they can be stripped off, so as to evaluate the stripping property. The evaluation results are shown in the following Table 1, Table 2 and Table 3, and the evaluation standards are as follows: [0042] Excellent ◯: It can be stripped off as a whole without broken fragments. [0043] Tolerable Δ: It can be stripped off, but it is also separated into small fragments. [0044] Poor x: It is totally unable to strip off.

TABLE-US-00001 TABLE 1 Experimental Experimental Experimental Experimental Component Type Example 1 Example 2 Example 3 Example 4 Polyurethane DM5433H 65 wt %  (meth)acrylate DM553 65 wt %  resin CN966-J75 65 wt %  DM5232 65 wt %  Filler Acetyl cellulose 4 wt % 4 wt % 4 wt % 4 wt % Diluent HEA 12 wt %  12 wt %  (monofunctional monomer) HEMA 12 wt %  12 wt %  (monofunctional monomer) TMP3EOTA 4 wt % 4 wt % 4 wt % (trifunctional monomer) G3POTA 4 wt % (trifunctional monomer) HDDA 5 wt % (difimctional monomer) EGDMA 5 wt % (difunctional monomer) NPG2PODA 5 wt % (difunctional monomer) DPGDA 5 wt % (difunctional monomer) HEMAP 4 wt % 4 wt % (monofunctional monomer) AA 4 wt % 4 wt % (monofunctional monomer) Surface curing Karenz MT PE1 3 wt % 3 wt % 3 wt % 3 wt % accelerating (thiol resin) agent Photo initiator Irgacure ® 2 wt % 2 wt % 2 wt % 2 wt % TPO-L Colorant 1 wt % 1 wt % 1 wt % 1 wt % Total 100 wt %  100 wt %  100 wt %  100 wt %  Evaluation Evaluation 1: ∘ ∘ ∘ ∘ results curing and drying properties evaluation after light irradiation Evaluation 2: ∘ ∘ ∘ ∘ stripping property evaluation Gel type One-step gel One-step gel One-step gel One-step gel

TABLE-US-00002 TABLE 2 Comparative Comparative Comparative Comparative Comparative Comparative Component Type Example a Example b Example c Example d Example e Example f polyurethane DM5433H 45 wt %  (meth)acrylate DM553 45 wt %  resin CN966-J75 45 wt %  DM5232 45 wt %  6113 60 wt %  6127 60 wt %  Filler Acetyl cellulose 3.5% 3.5% 3.5% 3.5% 5 wt % 5 wt % Diluent HEA 13.5 wt %   13.5 wt %   13.5 wt %   15 wt %  (monofunctional monomer) IBOA 13.5 wt %   (monofunctional monomer) HEMA 13.5 wt %   (monofunctional monomer) TMP3EOTA 8 wt % 8 wt % 8 wt % 8 wt % (trifunctional monomer) G3POTA 8 wt % 8 wt % (trifunctional monomer) HDDA 12 wt %  3 wt % (difunctional monomer) EGDMA 12 wt %  (difunctional monomer) NPG2PODA 12 wt %  3 wt % (difunctional monomer) DPGDA 12 wt %  (difunctional monomer) HEMAP 10 wt %  10 wt %  1 wt % (monofunctional monomer) AA 10 wt %  10 wt %  1 wt % (monofunctional monomer) Surface curing Karenz MT PE1 5 wt % 5 wt % 5 wt % 5 wt % 5 wt % 5 wt % accelerating (thiol resin) agent Photo initiator Irgacure ® TPO-L 2 wt % 2 wt % 2 wt % 2 wt % 2 wt % 2 wt % Colorant 1 wt % 1 wt % 1 wt % 1 wt % 1 wt % 1 wt % Total 100 wt %  100 wt %  100 wt %  100 wt %  100 wt %  100 wt %  Evaluation Evaluation 1: Δ x x Δ Δ Δ results curing and drying properties evaluation after light irradiation Evaluation 2: Δ x x Δ x x stripping property evaluation Gel type One-step gel One-step gel One-step gel One-step gel One-step gel One-step gel

TABLE-US-00003 TABLE 3 Commercially Commercially Commercially Commercially available available available available product A product B product C product D Evaluation Evaluation 1 Δ x x Δ results curing and drying properties evaluation after light irradiation Evaluation 2: x x x x stripping property evaluation Gel type One-step gel One-step gel Three-step gel Three -step gel

[0045] As shown in Table 1, Experimental Examples 1 to 4 are photo-curing nail gel composition of the invention, which is a one-step gel having properties of adhesion, beautification and scratch resistance. Besides, the photo-curing nail gel compositions of Experimental Examples 1 to 4 are totally cured under irradiation with a light source (LED) having a wavelength of 320 nm to 400 nm for 30 seconds with fast-curing property. As for adhesion, the photo-curing nail gel compositions of Experimental Examples 1 to 4 do not detach from the nail in about 7 days. In addition, the photo-curing nail gel compositions of Experimental Examples 1 to 4 can be easily stripped off as a whole by fingers without broken fragments after cured by irradiation, so the nail gel can be removed without removal reagent. Therefore, the stripping property of the photo-curing nail gel compositions of Experimental Examples 1 to 4 is good.

[0046] On the contrary, in the photo-curing nail gel compositions of Comparative Examples a to f, the content of each component is out of the range of content of each component in the photo-curing nail gel composition of the invention. Therefore, the curing and drying properties of Comparative Examples a to f under irradiation with a light source (LED) having a wavelength of 320 nm to 400 nm for 30 seconds are poor, and the stripping property is also poor. More specifically, the total content of the monofunctional monomer, the difunctional monomer, and the trifunctional monomer in Comparative Example b and c is higher than 40 wt %, so Comparative Example b and c can't be cured under irradiation with a light source (LED) having a wavelength of 320 nm to 400 nm for 30 seconds with poor curing property, and Comparative Example b and c can't be removed by stripping procedure.

[0047] Based on the above, the photo-curing nail gel composition of the invention is a one-step gel having properties of adhesion, beautification and scratch resistance, so as to achieve the purpose of adhesion, beautification and scratch resistance by single nail gel. Therefore, the complicated nail coating steps of traditional three-step nail gel can be simplified, so as to achieve the purpose of saving manual labor and time. As for the adhesion property, the adhesion time is about 7 days. Besides, the photo-curing nail gel composition of the invention is totally cured under irradiation with a light source having a wavelength of 320 nm to 400 nm for 30 seconds with fast-curing property. On the other hand, the photo-curing nail gel composition of the invention can be stripped off without broken fragments, so the nail gel can be easily removed without removal reagent. As a result, it not only simplifies the traditional nail gel removal process which costs manual labor and time, but also lowers the possibility of nail damage during nail gel removal process.

[0048] It will be apparent to those skilled in the art that various modifications and variations can be made to the structure of the present invention without departing from the scope or spirit of the invention. In view of the foregoing, it is intended that the present invention cover modifications and variations of this invention provided they fall within the scope of the following claims and their equivalents.