JP2018046900A - Drawing tool - Google Patents
Drawing tool Download PDFInfo
- Publication number
- JP2018046900A JP2018046900A JP2016182663A JP2016182663A JP2018046900A JP 2018046900 A JP2018046900 A JP 2018046900A JP 2016182663 A JP2016182663 A JP 2016182663A JP 2016182663 A JP2016182663 A JP 2016182663A JP 2018046900 A JP2018046900 A JP 2018046900A
- Authority
- JP
- Japan
- Prior art keywords
- composition
- parts
- meth
- acrylate
- drawing tool
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
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- 238000005259 measurement Methods 0.000 claims description 3
- 230000009974 thixotropic effect Effects 0.000 abstract description 3
- 238000007599 discharging Methods 0.000 abstract description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 19
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- 230000000052 comparative effect Effects 0.000 description 6
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- ZIUHHBKFKCYYJD-UHFFFAOYSA-N n,n'-methylenebisacrylamide Chemical compound C=CC(=O)NCNC(=O)C=C ZIUHHBKFKCYYJD-UHFFFAOYSA-N 0.000 description 1
- 239000012860 organic pigment Substances 0.000 description 1
- 229940105570 ornex Drugs 0.000 description 1
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- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 1
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- 229920001223 polyethylene glycol Polymers 0.000 description 1
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- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- KCTAWXVAICEBSD-UHFFFAOYSA-N prop-2-enoyloxy prop-2-eneperoxoate Chemical compound C=CC(=O)OOOC(=O)C=C KCTAWXVAICEBSD-UHFFFAOYSA-N 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
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- UWHCKJMYHZGTIT-UHFFFAOYSA-N tetraethylene glycol Chemical compound OCCOCCOCCOCCO UWHCKJMYHZGTIT-UHFFFAOYSA-N 0.000 description 1
- YRHRIQCWCFGUEQ-UHFFFAOYSA-N thioxanthen-9-one Chemical class C1=CC=C2C(=O)C3=CC=CC=C3SC2=C1 YRHRIQCWCFGUEQ-UHFFFAOYSA-N 0.000 description 1
- 210000003813 thumb Anatomy 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- DWWMSEANWMWMCB-UHFFFAOYSA-N tribromomethylsulfonylbenzene Chemical compound BrC(Br)(Br)S(=O)(=O)C1=CC=CC=C1 DWWMSEANWMWMCB-UHFFFAOYSA-N 0.000 description 1
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Images
Landscapes
- Cosmetics (AREA)
Abstract
Description
本発明は、爪やアクセサリーの表面に立体的で緻密な絵や文字が描ける描画具に関する。 The present invention relates to a drawing tool capable of drawing three-dimensional and precise pictures and characters on the surfaces of nails and accessories.
近年、ネイルアートの分野において、マニキュアに代わって、ジェルネイルが盛んになってきている。これは、ジェルネイルが、マニキュアと比較べて、持ち(耐久性)、ツヤ(発色がよい。)、強度(爪の強度を高める。)などの点で優れているからである。 In recent years, gel nails have become popular in the nail art field, replacing manicure. This is because gel nails are superior to nail polish in terms of holding (durability), gloss (good color development), strength (increasing nail strength), and the like.
ジェルネイルは、光硬化性樹脂を含むジェルネイル用組成物で爪に絵を描き、爪にUVライト(蛍光灯・LED)を照射して、光硬化性樹脂を硬化することによって、絵を爪に定着させる。そして、ジェルネイルの剥離性、表面の強度、抗菌性を高めるなどの目的のため、ジェルネイル用組成物について従来から様々な開発がなされてきている(特許文献1〜6を参照)。 Gel nail is a composition for gel nails containing a photo-curable resin. The nail is painted on the nail, and UV light (fluorescent light / LED) is applied to the nail to cure the photo-curable resin. To settle. Various developments have been made on gel nail compositions for the purpose of enhancing gel nail peelability, surface strength and antibacterial properties (see Patent Documents 1 to 6).
しかし、従来からあるジェルネイル用組成物は、粘性のある流動体であり、重力で自ら水平になろうとする性質がある。そのため、立体的で緻密な絵や文字をジェルネイルで描くのは困難であった。 However, conventional gel nail compositions are viscous fluids and have the property of trying to level themselves by gravity. Therefore, it is difficult to draw three-dimensional and precise pictures and characters with gel nails.
本発明は、爪やアクセサリーの表面に立体的で緻密な絵や文字を描ける描画具を提供することを課題とする。 This invention makes it a subject to provide the drawing tool which can draw a three-dimensional and precise picture and character on the surface of a nail | claw or an accessory.
発明者らは、鋭意検討の結果、光硬化性と高チクソ性とを備えた描画用組成物を特定の容器に収容した描画具を使用すれば、爪やアクセサリーの表面に立体的で緻密な絵や文字が描けることを見出し、本発明を完成させた。 As a result of intensive studies, the inventors have found that a drawing tool containing a photocurable and highly thixotropic composition contained in a specific container is three-dimensional and dense on the surfaces of nails and accessories. The present invention was completed by discovering that pictures and characters can be drawn.
すなわち、本発明の描画具は、描画用組成物を収容する収容部と、収容部に連結するとともに、収容部から供給された描画用組成物を外部に放出する開口部を有するノズル部と、を備える描画具であって、描画用組成物が光硬化性と高チクソ性とを備えるものである。なお、描画用組成物としては、そのチクソ比が1.3以上かつ3.5以下であるものが好ましく、光硬化性樹脂と増粘剤を含むものが例示できる。また、開口部の直径は、0.5mm以上かつ1.2mm以下であるのが好ましい。 That is, the drawing tool of the present invention is a storage unit that stores the drawing composition; a nozzle unit that is connected to the storage unit and has an opening that discharges the drawing composition supplied from the storage unit to the outside; The drawing composition is provided with photocurability and high thixotropy. In addition, as a composition for drawing, that whose thixo ratio is 1.3 or more and 3.5 or less is preferable, and a thing containing photocurable resin and a thickener can be illustrated. The diameter of the opening is preferably 0.5 mm or more and 1.2 mm or less.
本発明の描画具を使用すれば、爪やアクセサリーの表面に立体的で緻密な絵や文字が描ける。これにより、ネイルアーティストの表現領域が広がり、ネイルサロンなどのネイル業界の発展にも寄与することができる。 If the drawing tool of this invention is used, a three-dimensional and precise picture and character can be drawn on the surface of a nail or an accessory. This expands the range of expression for nail artists and can contribute to the development of the nail industry such as a nail salon.
本発明の描画具は、収容容器の収容部に描画用組成物を収容したものである。そこで、収容容器及び描画用組成物について、図に基づいて、以下に詳説する。なお、以下の実施の形態は、いかなる意味でも本発明の特許請求の範囲を限定するものではない。 The drawing tool of this invention accommodates the composition for drawing in the accommodating part of an accommodation container. Therefore, the container and the composition for drawing will be described in detail below based on the drawings. The following embodiments do not limit the scope of the claims of the present invention in any way.
1.収容容器
図1は、収容容器の一つの実施の形態を示した図である。また、図2は、描画具の別の実施の形態を示した図である。なお、図1(a)及び図2(a)は、描画具の不使用時の使用時の状態を示している。また、図1(b)及び図2(b)は、描画具の使用時の状態を示している。さらに、図1(c)及び図2(c)は、描画具を分解した分解時の状態を示している。
1. Storage Container FIG. 1 is a view showing an embodiment of a storage container. FIG. 2 is a diagram showing another embodiment of the drawing tool. FIGS. 1A and 2A show a state when the drawing tool is not used. Moreover, FIG.1 (b) and FIG.2 (b) have shown the state at the time of use of a drawing tool. Furthermore, FIG.1 (c) and FIG.2 (c) have shown the state at the time of decomposition | disassembly which decomposed | disassembled the drawing tool.
図1及び図2に示すように、収容容器1、2は、描画用組成物を収容する収容部11、21と、収容部11、21と連結しているノズル部12、22と、ノズル部12、22の先端を保護するキャップ部13、23から構成されている。
As shown in FIGS. 1 and 2, the
(1)収容部
収容部11、21は、指で押すと変形する程度の柔軟性があり、遮光性のプラスチックから構成されている。そのため、収容容器1、2中の描画用組成物は、日光などによって意図せずに硬化することなく、円筒形の側面を指で押せば、描画用組成物がノズル部12、22の方に向かって移動する。
(1) Accommodating portion The
(2)ノズル部
ノズル部12、22は、遮光性のプラスチックから構成されており、その一端は収容部11、21にネジ止め可能であり、その他端は先端に向かって狭くなっているとともに、収容部11、21から移動してきた描画用組成物を放出するための開口部が設けられている。なお、開口部の直径は、0.5mm以上かつ1.2mm以下であることが好ましい。開口部の直径が前記範囲内であれば、繊細な描写ができるからである。
(2) Nozzle portion The
(3)キャップ部
キャップ部13、23は、遮光性のプラスチックから構成されている。そのため、ノズル部12、22の開口部から異物が進入すること、開口部から入ってきた日光などによって、描画用組成物がノズル部12、22内で意図せずに硬化することを防げる。
(3) Cap part The
(4)他の態様
なお、本発明の描画具を構成する収容容器は、この他にも、例えば、収容部とノズル部とが一体成型されていてもよく、使いきり目薬の容器のように、ノズル部の先端が手で簡単に切り離し可能な使いきり容器であってもよい。
(4) Other Embodiments In addition to this, the storage container constituting the drawing tool of the present invention may be, for example, a storage part and a nozzle part that are integrally molded, such as a single-use eye drop container. A single-use container in which the tip of the nozzle portion can be easily separated by hand may be used.
2.描画用組成物
描画用組成物は、光硬化性と高チクソ性とを備えた樹脂組成物であり、より具体的には、光硬化性樹脂と増粘剤とを含む樹脂組成物が例示できる。なお、本発明書において、光硬化性とは、ジェルネイルで使用する人体に比較的無害な波長のUVライト(蛍光灯・LED)や太陽光を照射すると、紫外線や可視光線によって硬化するという意味である。また、本明細書において、高チクソ性とは、硬化前の樹脂組成物の粘度を測定し、測定した粘度から算出されたチクソ比が、特定の範囲内に入るという意味である。
2. Drawing composition The drawing composition is a resin composition having photocurability and high thixotropy, and more specifically, a resin composition containing a photocurable resin and a thickener can be exemplified. . In the present invention, photo-curing means that the human body used in gel nails is cured by ultraviolet light or visible light when irradiated with UV light (fluorescent lamp / LED) or sunlight having a relatively harmless wavelength. It is. In the present specification, high thixotropy means that the viscosity of the resin composition before curing is measured, and the thixo ratio calculated from the measured viscosity falls within a specific range.
より具体的には、後述する実施例の方法で測定した硬化前の描画用組成物の粘度を、25℃、2rpmで測定した場合が7,000〜2,200,000であり、25℃、4rpmで測定した場合が5,000〜700,000あって、両者の比であるチクソ比(2rpmにおける粘度/4rpmにおける粘度)が、1.3以上かつ3.5以下であるのが好ましい、という意味である。なお、25℃、4rpmにおける粘度が、5,000以下であれば描画線が垂れてしまい、700,000以上では描画線がかすれてしまう。 More specifically, the viscosity of the composition for drawing before curing measured by the method of Examples described later is 7,000 to 2,200,000 when measured at 25 ° C. and 2 rpm, and may be measured at 25 ° C. and 4 rpm. It means that it is preferably 5,000 to 700,000, and the thixo ratio (viscosity at 2 rpm / 4 viscosity at 2 rpm) is 1.3 or more and 3.5 or less. If the viscosity at 25 ° C. and 4 rpm is 5,000 or less, the drawn line droops, and if it is 700,000 or more, the drawn line is blurred.
(1)光硬化性樹脂
描画用組成物を構成する光硬化性樹脂としては、UVライトや太陽光を照射すると、紫外線や可視光線によって光重合(フォトポリマリゼーション)反応して硬化し、化粧品等の人体に触れる分野で使用可能な公知の樹脂であれば、限定することなく使用できる。このような光硬化性樹脂は、1)光硬化性成分(光重合性モノマー等)、2)光重合開始剤、3)溶媒などを一般的に含んでいる。そこで、各成分について以下に詳説する。
(1) Photo-curing resin As photo-curing resin constituting the composition for drawing, when UV light or sunlight is irradiated, it is cured by photopolymerization (photopolymerization) reaction with ultraviolet light or visible light, and cosmetics. Any known resin that can be used in the field of touching the human body can be used without limitation. Such a photocurable resin generally contains 1) a photocurable component (such as a photopolymerizable monomer), 2) a photopolymerization initiator, and 3) a solvent. Therefore, each component will be described in detail below.
1)光硬化性成分
光硬化性成分は、具体的には、光重合性モノマーとこれと相溶性のあるオリゴマー、ポリマーが挙げられる。光重合性モノマーは、光により架橋や重合できる官能基、例えば(メタ)アクリロイル基を有し、化粧品等の人体に触れる分野で使用可能な公知のモノマーであれば、特に制限することなく使用することができる。
1) Photocurable component Specific examples of the photocurable component include a photopolymerizable monomer and an oligomer or polymer compatible with the photopolymerizable monomer. The photopolymerizable monomer is not particularly limited as long as it is a known monomer that has a functional group that can be crosslinked or polymerized by light, such as a (meth) acryloyl group, and can be used in the field of touching the human body such as cosmetics. be able to.
(メタ)アクリロイル基を含む光重合性モノマーとして、具体的には、メチル(メタ)アクリレート、エチル(メタ)アクリレート、2-エチルヘキシル(メタ)アクリレート、2-ヒドロキシエチル(メタ)アクリレート、2-ヒドロキシプロピル(メタ)アクリレート、2-ヒドロキシエチル(メタ)アクリルアミド、エチレングリコールジ(メタ)アクリレート、トリエチレングリコールジ(メタ)アクリレート、テトラエチレングリコールジ(メタ)アクリレート、プロピレングリコールジ(メタ)アクリレート、トリメチロールプロパントリ(メタ)アクリレート、テトラメチロールプロパンテトラ(メタ)アクリレート、ペンタエリトリトールトリ(メタ)アクリレート、ペンタエリトリトールテトラ(メタ)アクリレート、ジペンタエリトリトールペンタ(メタ)アクリレート、ジペンタエリトリトールヘキサ(メタ)アクリレ−ト、1,6-ヘキサンジオールジ(メタ)アクリレート、イソボルニルアクリレート、ベンジル(メタ)アクリレート、カルドエポキシジ(メタ)アクリレート、N,N'-メチレンビスアクリルアミドが挙げられる。 Specific examples of the photopolymerizable monomer containing a (meth) acryloyl group include methyl (meth) acrylate, ethyl (meth) acrylate, 2-ethylhexyl (meth) acrylate, 2-hydroxyethyl (meth) acrylate, and 2-hydroxy Propyl (meth) acrylate, 2-hydroxyethyl (meth) acrylamide, ethylene glycol di (meth) acrylate, triethylene glycol di (meth) acrylate, tetraethylene glycol di (meth) acrylate, propylene glycol di (meth) acrylate, tri Methylolpropane tri (meth) acrylate, tetramethylolpropane tetra (meth) acrylate, pentaerythritol tri (meth) acrylate, pentaerythritol tetra (meth) acrylate, dipentaerythritol Ritolol penta (meth) acrylate, dipentaerythritol hexa (meth) acrylate, 1,6-hexanediol di (meth) acrylate, isobornyl acrylate, benzyl (meth) acrylate, cardoepoxy di (meth) acrylate, N, N'-methylenebisacrylamide is mentioned.
また、光重合性モノマーと相溶性のあるオリゴマーは、化粧品などの原料として販売されている公知のものであれば、特に限定することなく使用できる。具体的には、(メタ)ウレタンアクリレートオリゴマー、(メタ)ポリエステルオリゴマー、(メタ)エポキシアクリレートオリゴマー、ウレタン構造を有するポリマーなどが挙げられる。光重合性モノマーと相溶性のあるポリマーは上記モノマー、オリゴマーと相溶性のある樹脂類であって、具体的には(メタ)アクリレート(共)重合体、ポリスチレン、ポリ酢酸ビニル、ポリビニルピロリドン、ポリジアリルフタレート、ポリブタジエン、ポリイソプレン、スチレンブタジエンゴム、ブチルゴム、石油樹脂、ロジン、ロジンエステル樹脂、フェノール樹脂などがあげられる。 In addition, any oligomer that is compatible with the photopolymerizable monomer can be used without particular limitation as long as it is a known one that is sold as a raw material for cosmetics and the like. Specific examples include (meth) urethane acrylate oligomers, (meth) polyester oligomers, (meth) epoxy acrylate oligomers, and polymers having a urethane structure. Polymers compatible with the photopolymerizable monomer are resins compatible with the above monomers and oligomers. Specifically, (meth) acrylate (co) polymer, polystyrene, polyvinyl acetate, polyvinylpyrrolidone, poly Examples include diallyl phthalate, polybutadiene, polyisoprene, styrene butadiene rubber, butyl rubber, petroleum resin, rosin, rosin ester resin, and phenol resin.
2)光重合開始剤
光重合開始剤は、紫外線や可視光線等による光硬化性成分の光硬化反応を促進する公知の光重合開始剤であり、化粧品等の人体に触れる分野で使用可能な重合開始剤であれば、特に制限することなく使用することができる。
2) Photopolymerization initiator The photopolymerization initiator is a known photopolymerization initiator that accelerates the photocuring reaction of the photocurable component by ultraviolet rays or visible light, and can be used in the field of touching the human body such as cosmetics. Any initiator can be used without particular limitation.
光重合開始剤として、具体的には、1-ヒドロキシシクロヘキシルフェニルケトン、ベンゾフェノン、4,4'-ビス(ジメチルアミノ)ベンゾフェノン、3,3-ジメチル-4-メトキシ−ベンゾフェノン等のベンゾフェノン誘導体、アントラキノン、2-メチルアントラキノン、2-エチルアントラキノン、tert-ブチルアントラキノン等のアントラキノン誘導体、ベンゾイン、ベンゾインメチルエーテル、ベンゾインエチルエーテル、ベンゾインプロピルエーテル等のベンゾインアルキルエーテル誘導体、アセトフェノン、2,2-ジメトキシ-2-フェニルアセトフェノン、2,2-ジエトキシアセトフェノン等のアセトフェノン誘導体、2-クロロチオキサントン、ジエチルチオキサントン、イソプロピルチオキサントン、ジイソプロピルチオキサントン等のチオキサントン誘導体、アセトフェノン、2,2-ジメトキシ-2-フェニルアセトフェノン、2-ヒドロキシ−2-メチルプロピオフェノン、4'-イソプロピル-2-ヒドロキシ-2-メチルプロピオフェノン、2-メチル-1-〔4-(メチルチオ)フェニル〕-2-モルホリノ-1-プロパン等のアセトフェノン誘導体、ミヒラーズケトン、2,4,6-(トリハロメチル)トリアジン、2-(o-クロロフェニル)-4,5-ジフェニルイミダゾリル二量体、9-フェニルアクリジン、1,7-ビス(9-アクリジニル)ヘプタン、1,5-ビス(9-アクリジニル)ペンタン、1,3-ビス(9-アクリジニル)プロノパン、ジメチルベンジルケタール、トリメチルベンゾイルジフェニルホスフィンオキシド、トリブロモメチルフェニルスルホン、2-ベンジル-2-ジメチルアミノ-1-(4-モルホリノフェニル)-ブタン-1-オンなどが挙げられる。 Specific examples of photopolymerization initiators include 1-hydroxycyclohexyl phenyl ketone, benzophenone, 4,4′-bis (dimethylamino) benzophenone, benzophenone derivatives such as 3,3-dimethyl-4-methoxy-benzophenone, anthraquinone, Anthraquinone derivatives such as 2-methylanthraquinone, 2-ethylanthraquinone, tert-butylanthraquinone, benzoin alkyl ether derivatives such as benzoin, benzoin methyl ether, benzoin ethyl ether, benzoin propyl ether, acetophenone, 2,2-dimethoxy-2-phenyl Acetophenone derivatives such as acetophenone and 2,2-diethoxyacetophenone, and thioxanthone derivatives such as 2-chlorothioxanthone, diethylthioxanthone, isopropylthioxanthone and diisopropylthioxanthone , Acetophenone, 2,2-dimethoxy-2-phenylacetophenone, 2-hydroxy-2-methylpropiophenone, 4'-isopropyl-2-hydroxy-2-methylpropiophenone, 2-methyl-1- [4- Acetophenone derivatives such as (methylthio) phenyl] -2-morpholino-1-propane, Michler's ketone, 2,4,6- (trihalomethyl) triazine, 2- (o-chlorophenyl) -4,5-diphenylimidazolyl dimer, 9-phenylacridine, 1,7-bis (9-acridinyl) heptane, 1,5-bis (9-acridinyl) pentane, 1,3-bis (9-acridinyl) pronopan, dimethylbenzyl ketal, trimethylbenzoyldiphenylphosphine oxide , Tribromomethylphenylsulfone, 2-benzyl-2-dimethylamino-1- (4-morpholinophenyl) -butan-1-one, and the like.
3)溶媒
溶媒は、光硬化性成分や光重合開始剤等を溶解でき、化粧品等の人体に触れる分野で使用可能な溶媒であれば、特に制限することなく使用することができる。
3) Solvent The solvent can be used without particular limitation as long as it can dissolve a photocurable component, a photopolymerization initiator, and the like and can be used in the field of touching the human body such as cosmetics.
溶媒として、具体的には、エチレングリコールモノメチルエーテル、エチレングリコールモノブチルエーテル、プロピレングリコールモノメチルエーテル、ジエチレングリコールモノエチルエーテル、ジプロピレングリコールモノメチルエーテル等のエーテル系溶媒及びこれらのアセテート系溶媒、酢酸メチル、酢酸ブチル等のエステル系溶媒、メチルエチルケトン、メチルイソブチルケトン、シクロヘキサノン、ヒドオキシメチルフェニルプロパノン、ヒドロキシシクロヘキシルフェニルケトン等のケトン系溶媒などが挙げられる。 Specific examples of the solvent include ether solvents such as ethylene glycol monomethyl ether, ethylene glycol monobutyl ether, propylene glycol monomethyl ether, diethylene glycol monoethyl ether, dipropylene glycol monomethyl ether, and their acetate solvents, methyl acetate, butyl acetate. And ester solvents such as methyl ethyl ketone, methyl isobutyl ketone, cyclohexanone, hydroxymethylphenylpropanone, and ketone solvents such as hydroxycyclohexyl phenyl ketone.
なお、光硬化性樹脂は単独で使用してもよく、複数の異なる種類の光硬化性樹脂を混ぜ合わせて使用してもよい。また、描画用組成物における光硬化性樹脂の含有量は、描画用組成物の粘度やチクソ比が前記の範囲に入るように、使用する光硬化性樹脂や増粘剤の種類に応じて自由に変えることができる。 In addition, a photocurable resin may be used independently and may mix and use several different types of photocurable resins. In addition, the content of the photocurable resin in the drawing composition can be freely selected depending on the type of the photocurable resin and thickener used so that the viscosity and thixo ratio of the drawing composition fall within the above ranges. Can be changed to
(2)増粘剤
描画用組成物を構成する増粘剤としては、化粧品等の人体に触れる分野で使用可能な公知の増粘剤であれば特に限定することなく使用できる。このような増粘剤として、例えば、無機化合物、ワックス及びヒドロキシステアリン酸等が挙げられるが、これに限定されない。
(2) Thickener As a thickener which comprises a composition for drawing, if it is a well-known thickener usable in the field | area which touches human bodies, such as cosmetics, it can be used without limitation. Examples of such thickeners include, but are not limited to, inorganic compounds, waxes and hydroxystearic acid.
無機化合物として、具体的には、ホワイトカーボン、無水ケイ酸、ベントナイト、モンモリロナイト等が挙げられる。 Specific examples of the inorganic compound include white carbon, silicic anhydride, bentonite, and montmorillonite.
ワックスとして、具体的には、アマイドワックス、パラフィンワックス、セレシンワックス、マイクロクリスタリンワックス、水添マイクロクリスタリンワックス、フィッシャトロプシュワックス、ポリエチレンワックス、エチレン・プロピレンコポリマー、キャンデリラワックス、カルナウバワックス、ビーズワックス、モクロウ、ゲイロウ、ジロウ、モンタンワックス、ステアリル変性メチルポリシロキサン、ベヘニル変性メチルポリシロキサン等が挙げられる。 Specifically, amide wax, paraffin wax, ceresin wax, microcrystalline wax, hydrogenated microcrystalline wax, Fischer-Tropsch wax, polyethylene wax, ethylene / propylene copolymer, candelilla wax, carnauba wax, beeswax, Examples include mole, gallow, dirow, montan wax, stearyl-modified methylpolysiloxane, behenyl-modified methylpolysiloxane, and the like.
なお、増粘剤は、単独で使用してもよく、複数の異なる種類の増粘剤を混ぜ合わせて使用してもよい。また、描画用組成物における増粘剤の含有量は、描画用組成物の粘度やチクソ比が前記の範囲に入るように、使用する光硬化性樹脂や増粘剤の種類に応じて自由に変えることができる。 In addition, a thickener may be used independently and may mix and use a several different kind of thickener. Further, the content of the thickener in the drawing composition can be freely selected according to the type of photocurable resin and thickener used so that the viscosity and thixo ratio of the drawing composition fall within the above ranges. Can be changed.
(3)その他の成分
なお、描画用組成物は、上記成分の以外に、化粧品等の人体に触れる分野で使用可能な公知の顔料、充填剤、消泡剤、緩衝剤、キレート化剤、分散剤、防腐剤、湿潤剤等を、発明の効果を損なわない範囲で含んでいてもよい。
(3) Other components In addition to the above components, the drawing composition is a known pigment, filler, antifoaming agent, buffer, chelating agent, dispersion that can be used in the field of touching the human body such as cosmetics. Additives, preservatives, wetting agents and the like may be included as long as the effects of the invention are not impaired.
例えば、顔料としては、具体的に、二酸化チタン、弁柄等の金属酸化物系顔料、群青、紺青等の金属錯塩系顔料、カーボンブラック、その他の無機顔料や染料のレーキ顔料、アゾ系顔料、フタロシアニン系顔料、縮合多環系顔料等の有機顔料、さらには被覆マイカ等のパール顔料、アルミニウム蒸着ポリエチレンテレフタレートフィルム細片、その他のラメ素材、各種貝殻粉末、ブロンズ粉、その他の粉末などが挙げられる。また、充填剤としては、炭酸カルシウム、水酸化アルミニウム、硫酸バリウム、タルク、カオリン等が挙げられる。 For example, specific examples of the pigment include titanium dioxide, metal oxide pigments such as petals, metal complex pigments such as ultramarine and bitumen, carbon black, lake pigments of other inorganic pigments and dyes, azo pigments, Organic pigments such as phthalocyanine pigments and condensed polycyclic pigments, pearl pigments such as coated mica, aluminum vapor-deposited polyethylene terephthalate film strips, other lame materials, various shell powders, bronze powders, and other powders . Examples of the filler include calcium carbonate, aluminum hydroxide, barium sulfate, talc, and kaolin.
以下、この発明について実施例に基づいてより詳細に説明する。なお、この発明の特許請求の範囲は、以下の実施例によって如何なる意味においても制限されない。 Hereinafter, the present invention will be described in more detail based on examples. The claims of the present invention are not limited in any way by the following examples.
1.描画用組成物の調製
本発明で使用する描画用組成物(実施例1〜3)を調製した。なお、比較のため、従来からある描画用組成物も調製した。
1. Preparation of composition for drawing The composition for drawing (Examples 1-3) used by this invention was prepared. For comparison, a conventional drawing composition was also prepared.
実施例1
アロニックスM-1200(東亜合成:ウレタンアクリレート)60重量部、ペンタエリルトールトリアクリレート40重量部、1-6へキサンジオールジアクリレート20部、1-ヒドロキシ-シクロヘキシルフェニルケトン5重量部を混合したのち、ミズカシルP-707(水澤化学:ホワイトカーボン)12重量部を加え、高速攪拌機にて20分混合分散させ、光硬化性の描画用組成物を得た。
Example 1
After mixing 60 parts by weight of Aronix M-1200 (Toa Gosei: urethane acrylate), 40 parts by weight of pentaerythritol triacrylate, 20 parts of 1-6 hexanediol diacrylate, 5 parts by weight of 1-hydroxy-cyclohexyl phenyl ketone, 12 parts by weight of Mizukasil P-707 (Mizusawa Chemical: White Carbon) was added and mixed and dispersed with a high-speed stirrer for 20 minutes to obtain a photocurable drawing composition.
実施例2
アロニックスM-1200(東亜合成:ウレタンアクリレート)50重量部、ペンタエリルトールトリアクリレート30重量部、1-6へキサンジオールジアクリレート20部、1-ヒドロキシ-シクロヘキシルフェニルケトン5重量部を混合したのち、アエロジル200(EVONIK社製)5重量部を加え、高速攪拌機にて20分混合分散させ、光硬化性の描画用組成物を得た。
Example 2
After mixing 50 parts by weight of Aronix M-1200 (Toagosei: urethane acrylate), 30 parts by weight of pentaerythritol triacrylate, 20 parts of 1-6 hexanediol diacrylate, 5 parts by weight of 1-hydroxy-cyclohexyl phenyl ketone, Aerosil 200 (manufactured by EVONIK) (5 parts by weight) was added and mixed and dispersed with a high-speed stirrer for 20 minutes to obtain a photocurable drawing composition.
実施例3
EBECRYL4666(ダイセル・オルネクス社製 ウレタンアクリレート樹脂)60重量部、トリメチロールプロパントリアクリレート20重量部、イソボニルアクリレート10重量部、ビスフェノールAジアクリレート10重量部、2-ヒドロキシ2-メチル1-フェニル1-プロパノン5重量部を混合したのち、ASA-T-1800(伊藤製油社製 アマイドワックス)5重量部を加え、高速攪拌機にて20分混合分散させ、光硬化性の描画用組成物を得た。
Example 3
EBECRYL4666 (Daicel Ornex Urethane acrylate resin) 60 parts by weight, trimethylolpropane triacrylate 20 parts by weight, isobornyl acrylate 10 parts by weight, bisphenol A diacrylate 10 parts by weight, 2-hydroxy 2-methyl 1-phenyl 1- After mixing 5 parts by weight of propanone, 5 parts by weight of ASA-T-1800 (Amide Wax made by Ito Oil Co., Ltd.) was added, and the mixture was mixed and dispersed with a high-speed stirrer for 20 minutes to obtain a photocurable drawing composition.
比較例1
アロニックスM-1200(東亜合成:ウレタンアクリレート)60重量部、ペンタエリルトールトリアクリレート40重量部、1-6へキサンジオールジアクリレート20部、1-ヒドロキシ-シクロヘキシルフェニルケトン5重量部を混合したのち、ミズカシルP-707(水澤化学:ホワイトカーボン)3重量部を加え、高速攪拌機にて20分混合分散させ、光硬化性の描画用組成物を得た。
Comparative Example 1
After mixing 60 parts by weight of Aronix M-1200 (Toa Gosei: urethane acrylate), 40 parts by weight of pentaerythritol triacrylate, 20 parts of 1-6 hexanediol diacrylate, 5 parts by weight of 1-hydroxy-cyclohexyl phenyl ketone, 3 parts by weight of Mizukasil P-707 (Mizusawa Chemical: White Carbon) was added and mixed and dispersed with a high-speed stirrer for 20 minutes to obtain a photocurable drawing composition.
比較例2
アロニックスM-1200(東亜合成:ウレタンアクリレート)60重量部、ペンタエリルトールトリアクリレート40重量部、1-6へキサンジオールジアクリレート20部、1-ヒドロキシ-シクロヘキシルフェニルケトン5重量部を混合したのち、ミズカシルP-707(水澤化学:ホワイトカーボン)30重量部を加え、高速攪拌機にて20分混合分散させ、光硬化性の描画用組成物を得た。
Comparative Example 2
After mixing 60 parts by weight of Aronix M-1200 (Toa Gosei: urethane acrylate), 40 parts by weight of pentaerythritol triacrylate, 20 parts of 1-6 hexanediol diacrylate, 5 parts by weight of 1-hydroxy-cyclohexyl phenyl ketone, 30 parts by weight of Mizukasil P-707 (Mizusawa Chemical: White Carbon) was added and mixed and dispersed with a high-speed stirrer for 20 minutes to obtain a photocurable drawing composition.
2.チクソ比及び描画性の評価
実施例1〜3及び比較例1〜2の皮膜成形樹脂組成物のチクソ比及び描画性を調べた。具体的には、以下のようにして調べた。
2. Evaluation of thixo ratio and drawability The thixo ratio and drawability of the film-forming resin compositions of Examples 1 to 3 and Comparative Examples 1 and 2 were examined. Specifically, it investigated as follows.
(1)チクソ比の評価
本明細書中において、チクソ比は光硬化前の描画用組成物の数値を示し、光硬化前の描画用組成物の粘度に基づいて計算した。具体的には、描画用組成物の粘度を、粘度計(ブルックフィールド製PV-2T)、測定温度25℃、回転速度2rpmと4rpmの測定条件下で測定し、その比の値(2rpmにおける粘度/4rpmにおける粘度)をチクソ比とした。粘度とチクソ比の値を表1に示す。
(1) Evaluation of thixo ratio In this specification, the thixo ratio represents a numerical value of the drawing composition before photocuring, and was calculated based on the viscosity of the drawing composition before photocuring. Specifically, the viscosity of the composition for drawing was measured under a viscometer (Brookfield PV-2T), measurement temperature 25 ° C., measurement speeds of 2 rpm and 4 rpm, and the ratio value (viscosity at 2 rpm). (Viscosity at / 4 rpm) was defined as the thixo ratio. The values of viscosity and thixo ratio are shown in Table 1.
(2)描画性の評価
実施例1〜3及び比較例1〜2の皮膜成形樹脂組成物を図1に示すようなプラスチック容器(ノズル部の開口部の直径1.0mm)に収容して、描画具を得た。描画具でヒトの親指の爪に長さ約5mmの曲線を描いた。爪にLEDライト(電力8W)で紫外線(波長375nm)を2分から4分当てて、塗布された皮膜成形樹脂組成物を光硬化性した。描画した直線の広がりから、描画物の描画性を以下の基準に沿って目視で評価した。なお、立体的に描画するためには「○」であることが好ましい。描画性の評価結果を表1に示す。
(2) Evaluation of drawability The film-forming resin compositions of Examples 1 to 3 and Comparative Examples 1 to 2 are accommodated in a plastic container (diameter of the opening of the nozzle portion: 1.0 mm) as shown in FIG. I got the ingredients. I drew a curve about 5mm in length on the nail of a human thumb with a drawing tool. UV light (wavelength 375 nm) was applied to the nails with LED light (power 8 W) for 2 to 4 minutes to make the applied film-forming resin composition photocurable. From the spread of the drawn straight line, the drawability of the drawn object was visually evaluated according to the following criteria. Note that “◯” is preferable for three-dimensional drawing. Table 1 shows the evaluation results of the drawability.
評価基準
○:立体的に描画でき、光硬化性後も描画線の形状が変化しない。
△:立体的に描画できるものの、光硬化性後には描画線の形状が変化している。
×:描画し難い。
Evaluation Criteria ○: Three-dimensional drawing is possible, and the shape of the drawing line does not change even after photocuring.
(Triangle | delta): Although it can draw in three dimensions, after photocuring, the shape of the drawing line has changed.
X: It is difficult to draw.
表1から、実施例1〜3の皮膜成形樹脂組成物は、優れた描画性を有することが分かった。これに対して、比較例1の皮膜成形樹脂組成物は、描画はできたものの、すぐに液垂れて描画線が太くなり、不鮮明な描画になってしまった。また、比較例2の皮膜成形樹脂組成物は、描画し難く、線が描いている途中でかすれてしまった。 From Table 1, it turned out that the film-forming resin composition of Examples 1-3 has the outstanding drawing property. On the other hand, although the film-forming resin composition of Comparative Example 1 was able to draw, the liquid dripped immediately and the drawing line became thick, resulting in unclear drawing. Moreover, the film-forming resin composition of Comparative Example 2 was difficult to draw, and was faint in the middle of drawing the line.
1 、2 収容容器
11、21 収容部
12、22 ノズル部
13、23 キャップ部
1, 2
Claims (4)
収容部に連結するとともに、収容部から供給された描画用組成物を外部に放出する開口部を有するノズル部と、
を備える描画具であって、
描画用組成物が光硬化性と高チクソ性とを備えている描画具。 A housing for housing the drawing composition;
A nozzle part having an opening that is connected to the storage part and discharges the drawing composition supplied from the storage part to the outside;
A drawing tool comprising:
A drawing tool in which the drawing composition has photocurability and high thixotropy.
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| JP2016182663A JP2018046900A (en) | 2016-09-20 | 2016-09-20 | Drawing tool |
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| JP2016182663A JP2018046900A (en) | 2016-09-20 | 2016-09-20 | Drawing tool |
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Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2000053714A (en) * | 1998-08-05 | 2000-02-22 | Three Bond Co Ltd | Photo-curing resin composition for forming braille point |
| JP2008174743A (en) * | 2006-12-21 | 2008-07-31 | Cray Valley Sa | Rheological additive in form of preactivated paste |
-
2016
- 2016-09-20 JP JP2016182663A patent/JP2018046900A/en active Pending
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2000053714A (en) * | 1998-08-05 | 2000-02-22 | Three Bond Co Ltd | Photo-curing resin composition for forming braille point |
| JP2008174743A (en) * | 2006-12-21 | 2008-07-31 | Cray Valley Sa | Rheological additive in form of preactivated paste |
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