WO2018151460A1 - 접착층을 포함하는 담지체 및 담지체의 제조방법 - Google Patents

접착층을 포함하는 담지체 및 담지체의 제조방법 Download PDF

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Publication number
WO2018151460A1
WO2018151460A1 PCT/KR2018/001699 KR2018001699W WO2018151460A1 WO 2018151460 A1 WO2018151460 A1 WO 2018151460A1 KR 2018001699 W KR2018001699 W KR 2018001699W WO 2018151460 A1 WO2018151460 A1 WO 2018151460A1
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WIPO (PCT)
Prior art keywords
carrier
adhesive
adhesive layer
adhesive surface
cosmetic
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PCT/KR2018/001699
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English (en)
French (fr)
Inventor
정해원
백두현
이승환
최경호
Original Assignee
(주)아모레퍼시픽
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Application filed by (주)아모레퍼시픽 filed Critical (주)아모레퍼시픽
Priority to US16/485,987 priority Critical patent/US20200061965A1/en
Priority to JP2019543947A priority patent/JP2020507413A/ja
Priority to CN201880012256.0A priority patent/CN110337251A/zh
Publication of WO2018151460A1 publication Critical patent/WO2018151460A1/ko

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    • B32B2307/00Properties of the layers or laminate
    • B32B2307/70Other properties
    • B32B2307/716Degradable
    • B32B2307/7163Biodegradable
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2307/00Properties of the layers or laminate
    • B32B2307/70Other properties
    • B32B2307/732Dimensional properties

Definitions

  • the present invention relates to a support and a method for producing the support including an adhesive layer having excellent adhesion.
  • the low viscosity cosmetic composition is located in the pores of the porous carrier.
  • a carrier composed of two or more layers is used, and an adhesive layer is used for the adhesion between the layers.
  • the conventional adhesive layer has a problem that the adhesive strength is lowered due to the specific components of the cosmetic.
  • An object of the present invention is a carrier supporting a cosmetic, comprising: a first carrier having a first adhesive surface; A second carrier having a second adhesive surface facing the first adhesive surface; And an adhesive layer positioned between the first carrier and the second carrier to bond the first adhesive surface and the second adhesive surface, wherein the adhesive layer is formed of at least one of a polyolefin-based material and a polyester-based material. Is achieved by.
  • the cosmetic composition may further include a cosmetic material supported on the first carrier and the second carrier, and the cosmetic agent may include an alcohol component.
  • the first carrier and the second carrier may be a polyurethane foam.
  • the first carrier and the second carrier may be a polyether polyurethane foam.
  • the adhesive layer may be formed on front surfaces of the first adhesive surface and the second adhesive surface.
  • the adhesive layer may be partially formed on the first adhesive surface and the second adhesive surface.
  • the adhesive layer may include a low molecular fiber.
  • An object of the present invention is a method of manufacturing a carrier for carrying a cosmetic, comprising the steps of: providing a first carrier having a first adhesive surface and a second carrier having a second adhesive surface; Positioning an adhesive sheet between the first adhesive surface and the second adhesive surface; Melting the adhesive sheet to form an adhesive layer bonding the first adhesive surface and the second adhesive surface, wherein the adhesive sheet is achieved by at least one of a polyolefin-based material and a polyester-based material. .
  • the method may further include supporting the cosmetic on the first carrier and the second carrier, wherein the cosmetic may include an alcohol component.
  • the first carrier and the second carrier may be a polyurethane foam.
  • the adhesive sheet may include low molecular fiber.
  • a carrier and a method of manufacturing the carrier including an adhesive layer having excellent adhesion.
  • FIG. 1 is a perspective view of a carrier according to a first embodiment of the present invention
  • FIG. 2 is an exploded perspective view of a carrier according to a second embodiment of the present invention.
  • FIG. 3 is a cross-sectional view taken along line III-III ′ of FIG. 1;
  • FIG. 4 is a perspective view of a carrier according to a second embodiment of the present invention.
  • FIG. 5 is a perspective view of a carrier according to a third embodiment of the present invention.
  • FIG. 6 shows an embodiment of the carrier manufacturing method according to the invention
  • Figure 7 shows another embodiment of the carrier manufacturing method according to the present invention.
  • carrier means that it can carry a cosmetic, it can also be expressed as “mediator” or “carrier”. In addition, the “carrier” refers to both carrying and unsupporting cosmetics.
  • a carrier according to a first embodiment of the present invention will be described with reference to FIGS. 1 to 3.
  • FIG. 1 is a perspective view of a carrier according to a first embodiment of the present invention
  • Figure 2 is an exploded perspective view of the carrier according to a second embodiment of the present invention
  • Figure 3 is a cross-sectional view taken along III-III 'of FIG. to be.
  • the carrier 1 includes a first carrier 10, a second carrier 20, an adhesive layer 30, and a cosmetic 40.
  • the carrier 1 is generally thick disc-shaped.
  • the first supporting agent 10 has a discharge surface from which the cosmetics 40 are discharged.
  • the first carrier 10 and the second carrier 20 have a similar shape, and the thickness may be the same or different.
  • the cosmetic composition 40 is supported on the first carrier 10 and the second carrier 20.
  • the first adhesive surface 11 of the first carrier 10 and the second adhesive surface 21 of the second carrier 20 are bonded by an adhesive layer 30. As a result, the first carrier 10 and the second carrier 20 are bonded to each other.
  • the adhesive layer 30 is formed over the first adhesive surface 11 and the second adhesive surface 21.
  • the first carrier 10 and the second carrier 20 may be provided with the same or different materials.
  • the first carrier 10 and the second carrier 20 may be made of a porous material.
  • the porous material of the synthesis may be a foam.
  • the foam may be foamed by dry foam or wet foam, and the foam may contain fibers.
  • a natural porous material may be used a loofah, konjac, sponge
  • first carrier 10 and the second carrier 20 may be a synthetic or natural fiber material.
  • Natural fibers include, but are not limited to, cellulose, natural pulp, loofah, ramie, ramie (plants), ayate (rough grains of agave or palm trees), algae, and bamboo (Bamboo) , Sisal, sisal terry, konjac, Tencel TM fiber fabric (ten antibacterial tencel fiber made from eucalyptus wood), cotton felt, tencel cotton, manila hemp (abaca) fiber) or at least any one of the fibers.
  • Methylene terephthalate fibers, polyethylene, polypropylene, polyacrylates, polyacetates, polyolefins, PLA (polylactic acid), polylactic acid-based composite fibers (environmental biodegradable) may be made of at least one.
  • At least one of the first carrier 10 and the second carrier 20 may be a porous material, a WEB structure, a crimping structure, foaming, and a WEB structure or a foaming and crimping structure.
  • the first carrier 10 and the second carrier 20 carry the same cosmetic 40 or different cosmetics 40.
  • the cosmetic 40 is an emulsified composition, specifically, oil-in-water (W / O / W) or oil-in-water (O / W / O) or water-in-oil (W / O) or oil-in-water (O / W). ) Or dispersible compositions or specifically oil dispersion or water dispersion compositions.
  • At least one of the first carrier 10 and the second carrier 20 may be a polyether polyurethane foam.
  • the first carrier 10 and the second carrier 20 are both polyurethane foams and may have different pore sizes.
  • the multi-layer structure of the carrier 1 is used to soften the cosmetic by controlling the discharge of the cosmetic (40) to discharge a uniform amount or to change the discharge path of the cosmetic (40).
  • the multilayer structure of the carrier 1 may be used to prevent the phenomenon of the carrier 1 being darkened by the shadow of the pore by using an upper layer having a small pore size.
  • the lower layer has a larger pore size than the upper layer, and has excellent cosmetic support, and the lower layer may be thicker than the upper layer.
  • the cosmetic 40 may be, for example, a liquid composition or a solid composition, and in the case of the solid composition, may include a powder composition such as a powder.
  • the cosmetic composition may be, for example, a composition for makeup primer, a composition for makeup base, a composition for foundation, a composition for concealer, a composition for lip, a composition for lip liner, a composition for eyebrow, a composition for eye shadow, a composition for eyeliner, blusher It may be formulated into a composition for blusher, a composition for sunscreen, a composition for skin care, but is not limited thereto.
  • the cosmetic 40 may include alcohol to give a cooling feeling. Including alcohol can also reduce the amount of preservatives.
  • the alcohol may be, but is not limited to, ethanol.
  • the alcohol content in the cosmetic 40 may be 1 to 15% by weight, 3 to 12% by weight or 5 to 10% by weight.
  • the adhesive layer 30 is made of a component that is stable to alcohol, but is not limited thereto, and may be made of a polyolefin-based and polyester-based material. Specifically, the adhesive layer 30 may be formed by melting an adhesive in the form of a web of polyolefin-based or polyester-based material, and the adhesive in the form of a web may be net-spun in a sheet form. In addition, the adhesive layer 30 may include a low molecular fiber.
  • Fine through-holes are formed in the adhesive layer 30 so that the cosmetics 40 may move between the first carrier 10 and the second carrier 20.
  • the adhesive layer 30 is a stable component to alcohol, even if the cosmetic 40 including alcohol is used, the adhesion of the first carrier 10 and the second carrier 20 is stable.
  • the shape of the carrier 1 may be variously modified, such as a square plate, and may be composed of three or more layers.
  • FIG. 4 is a perspective view of a carrier according to a second embodiment of the present invention.
  • the adhesive layer 30 is distributed in a scattering manner, whereby the first adhesive surface 11 and the second adhesive surface 21 are partially bonded to each other.
  • FIG. 5 is a perspective view of a carrier according to a third embodiment of the present invention.
  • the adhesive layer 30 is partially formed with an empty portion, whereby the first adhesive surface 11 and the second adhesive surface 21 are partially bonded to each other.
  • the first carrier 10 and the second carrier 20 have a portion directly contacting each other without the adhesive layer 30 while being bonded to each other.
  • the cosmetic composition 40 may smoothly move between the first carrier 10 and the second carrier 20.
  • Figure 6 shows an embodiment of a carrier manufacturing method according to the present invention.
  • the first carrier 10, the second carrier 20, and the adhesive sheet 31 are prepared.
  • the adhesive sheet 31 is made of polyolefin or polyester, and has a thin sheet shape.
  • the adhesive sheet 31 may be a non-woven hot melt adhesive that net-emulates low-molecular fibers melted at a low temperature, and may have a web form.
  • the adhesive sheet 31 may exhibit adhesive performance at a relatively low temperature.
  • the softening point may be 105 ° C. or less, 110 ° C. or less, or 120 ° C. or less, and more specifically, 80 ° C. to 105 ° C. ° C, 80 ° C to 110 ° C or 80 ° C to 120 ° C.
  • the adhesive sheet 31 is positioned between the first carrier 10 and the second carrier 20 to melt the adhesive sheet 31. Melting may be performed using hot air, and the adhesion is performed while the adhesive sheet 31 is melted. The adhesive sheet 31 is melted to form an adhesive layer 30 and bonds the first carrier 10 and the second carrier 20.
  • the cosmetics are supported.
  • Pressing may be performed during or after melting to ensure adhesion.
  • Adhesion using the adhesive sheet 31 may be performed using an electric fusing press, a heated roll, hot air, radiant heat, or a steam press.
  • Thermal bonding temperature may be 105 °C to 125 °C.
  • Figure 7 shows another embodiment of the carrier manufacturing method according to the present invention.
  • the adhesive sheet 31 is placed on the second carrier 20 and melted to form an adhesive layer 30.
  • the first carrier 10 is positioned on the adhesive layer 30 and the first carrier 10 and the second carrier 20 are adhered to each other.
  • the manufacturing method described above may vary.
  • the shape and distribution of the adhesive sheet 31 may be variously changed, thereby changing the shape of the adhesive layer 30.
  • the adhesive layer 30 may be formed using various types of adhesive such as spherical adhesive or liquid adhesive without using the adhesive sheet 31.
  • Polyurethane foam As the first carrier 10, a polyurethane foam having a thickness of 1 mm was used.
  • Polyurethane foam is a wet urethane foam having a polyether and polyester of 5: 5 and containing polycarbonate diol and having enhanced chemical resistance.
  • a polyether-based polyurethane foam having a thickness of 8 mm was used as the second carrier 20 as the second carrier 20.
  • the adhesive layer 30 was formed using a polyester-based low temperature reactive adhesive sheet 31.
  • An isocyanate adhesive was used as a comparative example.
  • the adhesive layer 30 was formed over the first adhesive surface 11 and the second adhesive surface 21, and the adhesive sheet 31 was melted using hot air. After melting, they were pressed, washed and dried.
  • the separation strength of the alcohol was tested. Four alcohol solutions were used: 100% ethanol, 15% ethanol, 10% ethanol and 5% ethanol.
  • the carrier was left in an alcohol solution for 7 days in a 50 °C thermostat, and 2) it was checked for separation with tweezers. 3) if it was not separated with tweezers, the separation strength was measured after 90% or more of the contents were removed. (Measured by push pull gauge, the top side is fixed with forceps scissors or push pull forceps, and the bottom side is fixed with jig or hand) 4) When pulled to 0.4kg.f with push pull gauge, it was checked whether it was separated (push) Full gauge speed is 10mm / sec).
  • Example shows a large separation strength even in 100% ethanol solution shows that the carrier is stably bonded.

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Organic Chemistry (AREA)
  • Ceramic Engineering (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Textile Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Laminated Bodies (AREA)
  • Cosmetics (AREA)

Abstract

본 발명은 담지체와 담지체 제조방법에 관한 것이다. 본 발명에 따른 화장료를 담지하는 담지체는, 제1접착면을 가지는 제1담지체; 상기 제1접착면과 마주하는 제2접착면을 가지는 제2담지체; 및 상기 제1담지체와 상기 제2담지체 사이에 위치하여 상기 제1접착면와 상기 제2접착면을 접착시키는 접착층을 포함하며, 상기 접착층은 폴리올레핀계 재질 및 폴리에스테르계 재질 중 적어도 어느 하나로 이루어져 있다.

Description

접착층을 포함하는 담지체 및 담지체의 제조방법
본 발명은 접착력이 우수한 접착층을 포함하는 담지체 및 담지체의 제조방법에 관한 것이다.
종래 저점도 화장료 조성물, 특히, 액상의 화장료 조성물은 주로 진공 용기, 펌프 용기 또는 유리 용기 등에 충진되어 유통 및 보관되었다. 하지만 이들 용기들은 휴대가 불편하다는 단점이 있다. 따라서, 외출시에도 간편하게 화장을 하거나 수정할 필요성이 증가함에 따라, 휴대가 편리한 화장용구에 대한 요구가 있었다.
최근, 담지체에 저점도의 화장료 조성물을 담지시켜 휴대가 간편하게 만든 화장용구가 개발되었다. 이러한 화장용구에서 저점도의 화장료 조성물은 다공성 담지체의 포어 내에 위치하게 된다.
한편, 2층 이상으로 이루어진 담지체가 사용되고 있는데 이러한 담지체에는 각 층간의 접착을 위해 접착층이 사용되고 있다. 그런데 기존의 접착층은 화장료의 특정성분 등으로 인해 접착력이 저하되는 문제가 있다.
따라서 본 발명의 목적은 접착력이 우수한 접착층을 포함하는 담지체 및 담지체의 제조방법을 제공하는 것이다.
상기 본 발명의 목적은 화장료를 담지하는 담지체에 있어서, 제1접착면을 가지는 제1담지체; 상기 제1접착면과 마주하는 제2접착면을 가지는 제2담지체; 및 상기 제1담지체와 상기 제2담지체 사이에 위치하여 상기 제1접착면와 상기 제2접착면을 접착시키는 접착층을 포함하며, 상기 접착층은 폴리올레핀계 재질 및 폴리에스테르계 재질 중 적어도 어느 하나로 이루어진 것에 의해 달성된다.
상기 제1담지체와 상기 제2담지체에 담지되어 있는 화장료를 더 포함하며, 상기 화장료는 알코올 성분을 포함할 수 있다.
상기 제1담지체와 상기 제2담지체는 폴리우레탄 발포체일 수 있다.
상기 제1담지체와 상기 제2담지체는 폴리에테르계 폴리우레탄 발포체일 수 있다.
상기 접착층은 상기 제1접착면 및 상기 제2접착면의 전면에 형성되어 있을 수 있다.
상기 접착층은 상기 상기 제1접착면 및 상기 제2접착면에 부분적으로 형성되어 있을 수 있다.
상기 접착층은 저분자 섬유질을 포함할 수 있다.
상기 본 발명의 목적은 화장료를 담지하는 담지체의 제조방법에 있어서, 제1접착면을 가지는 제1담지체 및 제2접착면을 가지는 제2담지체를 마련하는 단계와; 상기 제1접착면 및 상기 제2접착면 사이에 접착 시트를 위치시키는 단계와; 상기 접착 시트를 용융시켜 상기 제1접착면과 상기 제2접착면을 접착시키는 접착층을 형성하는 단계를 포함하며, 상기 접착시트는 폴리올레핀계 재질 및 폴리에스테르계 재질 중 적어도 어느 하나로 이루어진 것에 의해 달성된다.
상기 접착층 형성 후 화장료를 상기 제1담지체와 상기 제2담지체에 담지하는 단계를 더 포함하며, 상기 화장료는 알코올 성분을 포함할 수 있다.
상기 제1담지체와 상기 제2담지체는 폴리우레탄 발포체일 수 있다.
상기 접착 시트는 저분자 섬유질을 포함할 수 있다.
본 발명에 따르면 접착력이 우수한 접착층을 포함하는 담지체 및 담지체의 제조방법이 제공된다.
도 1은 본 발명의 제1실시예에 따른 담지체의 사시도이고,
도 2는 본 발명의 제2실시예에 따른 담지체의 분해사시도이고,
도 3은 도 1의 III-III'를 따른 단면도이고,
도 4는 본 발명의 제2실시예에 따른 담지체의 사시도이고,
도 5는 본 발명의 제3실시예에 따른 담지체의 사시도이고,
도 6은 본 발명에 따른 담지체 제조방법의 일실시예를 나타낸 것이고,
도 7은 본 발명에 따른 담지체 제조방법의 다른 실시예를 나타낸 것이다.
이하 도면을 참조하여 본 발명을 더욱 상세히 설명한다.
첨부된 도면은 본 발명의 기술적 사상을 더욱 구체적으로 설명하기 위하여 도시한 일 예에 불과하므로 본 발명의 사상이 첨부된 도면에 한정되는 것은 아니다.
본 명세서에서 “담지체”는 화장료를 담지할 수 있는 것을 의미하며, “매개체” 또는 “운반체”로도 표현될 수 있다. 또한 “담지체”는 화장료를 담지하고 있는 것과 담지하고 있지 않은 것 모두를 나타낸다.
도 1 내지 도 3을 참조하여 본 발명의 제1실시예에 따른 담지체를 설명한다.
도 1은 본 발명의 제1실시예에 따른 담지체의 사시도이고, 도 2는 본 발명의 제2실시예에 따른 담지체의 분해사시도이고, 도 3은 도 1의 III-III'를 따른 단면도이다.
담지체(1)는 제1담지체(10), 제2담지체(20), 접착층(30) 및 화장료(40)를 포함한다. 담지체(1)는 전체적으로 두꺼운 원판형상이다. 제1담지제(10)는 화장료(40)가 배출되는 배출면을 가진다.
제1담지체(10)와 제2담지체(20)는 유사한 형태를 가지고 있으며, 두께는 서로 같거나 다를 수 있다. 화장료(40)는 제1담지체(10)와 제2담지체(20)에 담지되어 있다.
제1담지체(10)의 제1접착면(11)과 제2담지체(20)의 제2접착면(21)은 접착층(30)에 의해 접착되어 있다. 이에 의해 제1담지체(10)와 제2담지체(20)는 서로 접착되어 있다.
접착층(30)은 제1접착면(11)과 제2접착면(21)의 전체에 걸쳐 형성되어 있다.
제1담지체(10)와 제2담지체(20)는 동일하거나 서로 다른 재질로 마련될 수 있다.
제1담지체(10)와 제2담지체(20)는 다공성 재질로 마련될 수 있다. 예를 들어, 합성의 다공성 재질로는 발포폼일 수 있다. 발포 폼은 NBR(acrylonitrile-butadiene rubber), BR(Butadiene Rubber), SBR(Styrene Butadiene Rubber), NR(Natural Rubber), 습식우레탄, 건식 우레탄, 폴리에테르, 폴리에스테르, 폴리염화비닐, 폴리에틸렌, EVA(Ethylene Vinyl Acetate), 라텍스, 실리콘, SIS(Styrene Isoprene Styrene), SEBS(Styrene Ethylene Butylene Styrene), PVA(PolyVinyl Alcohol), 실리콘제 엘라스토머, 니트릴고무, 부틸 고무 및 네오프렌으로 구성된 군에서 선택되는 하나 이상 재질을 포함할 수 있으나 이에 한정되지 않는다. 발포 폼은 건식 발포방식 또는 습식 발포방식으로 발포될 수 있으며, 발포 폼은 파이버를 함유할 수도 있다. 또한, 천연의 다공성 재질로는 수세미, 곤약, 해면, 셀룰로오스, 바이오 셀룰로오스 또는 스코리아를 사용할 수 있다.
또한, 제1담지체(10)와 제2담지체(20)는 합성 또는 천연의 섬유 재질일 수 있다. 천연 섬유로는, 이에 한정되지 않으나, 셀룰로오스, 천연펄프, 수세미(loofah), 모시, 라미(식물), 아야테(ayate, 용설란 또는 야자나무의 거친 피륙), 조류(algae), 대나무(Bamboo), 사이잘(sisal), 사이잘 테리(sisal terry, 사이잘로 짠 천), 곤약, 텐셀TM 파이버 원단(유칼립투스 나무로 만든 천연 항균 기능의 텐셀 섬유), 코튼 펠트, 텐셀 솜, 마닐라 삼(abaca fiber) 중 적어도 어느 하나로 마련되거나, 적어도 어느 하나를 포함되어 이루어질 수 있다.
합성 섬유로는, 이에 한정되지는 않으나, 나일론, 아세테이트 섬유, 나일론 부직포, 카시미론 파이버(아크릴로니트릴CH2=CH-CN 섬유를 주요구성 성분으로 하는 합성섬유 즉 아크릴 섬유), 컴포트 파이버, 폴리트리메틸렌테레프탈레이트 섬유, 폴리에틸렌, 폴리프로필렌, 폴리아크릴레이트, 폴리아세테이트, 폴리올레핀, PLA(polylactic acid), 폴리유산계 복합 섬유(친환경 생분해성) 중 적어도 어느 하나로 이루어질 수 있다.
제1담지체(10)와 제2담지체(20)는 중 적어도 어느 하나는 다공성 재질, WEB구조, 권축 구조, 발포 및 WEB구조 또는 발포 및 권축 구조일 수 있다.
제1담지체(10)와 제2담지체(20)는 동일한 화장료(40)를 담지하고 있거나, 서로 다른 화장료(40)를 담지하고 있다. 화장료(40)은 유화형 조성물, 구체적으로 수중유중수(W/O/W)형 또는 유중수중유형(O/W/O)형 또는 유중수(W/O)형 또는 수중유(O/W)형 조성물, 분산형 조성물이거나 구체적으로는 유분산 또는 수분산 조성물일 수 있다.
제1담지체(10)와 제2담지체(20) 중 적어도 하나는 폴리에테르계 폴리우레탄 발포체일 수 있다. 또는, 제1담지체(10)와 제2담지체(20)는 모두 폴리우레탄 발포체이며 포어사이즈가 다를 수 있다.
담지체(1)의 다층구조는 화장료(40)의 배출량을 조절하여 균일한 양이 토출되게 하거나 화장료(40)의 배출 경로를 변화시켜 화장료를 부드럽게 해주기 위해 사용된다.
또한, 담지체(1)의 다층구조는 포어사이즈가 작은 상부층을 사용하여 포어의 그림자에 의해 담지체(1)가 어두워지는 현상을 방지하기 위해 사용되기도 한다. 이 경우 하부층은 상부층에 비해 포어사이즈가 커서 화장료 담지력이 우수하며, 하부층은 상부층에 비해 두꺼울 수 있다.
화장료(40)는, 예를 들어, 액상 조성물 또는 고상 조성물일 수 있으며, 고상 조성물일 경우, 분말과 같은 분체 조성물을 포함할 수 있다. 또한, 화장료 조성물은 예를 들면, 메이크업 프라이머용 조성물, 메이크업 베이스용 조성물, 파운데이션용 조성물, 컨실러용 조성물, 립용 조성물, 립 라이너용 조성물, 아이브로우용 조성물, 아이섀도우용 조성물, 아이라이너용 조성물, 블러셔(blusher)용 조성물, 자외선 차단제용 조성물, 스킨 케어용 조성물로 제형화될 수 있으나, 이에 한정되는 것은 아니다.
화장료(40)는 쿨링감을 주기 위해 알코올을 포함하고 있을 수 있다. 알코올을 포함시킬 경우 방부제의 함량을 줄일 수도 있다. 알코올은, 이에 한정되지 않으나, 에탄올일 수 있다. 화장료(40) 내의 알코올 함량은 1 내지 15중량%, 3 내지 12중량% 또는 5 내지 10중량%일 수 있다.
접착층(30)은 알코올에 안정한 성분으로 이루어지며, 이에 한정되지는 않으나 폴리올레핀계 및 폴리에스테르계 재질로 이루어질 수 있다. 구체적으로는, 접착층(30)은 폴리올레핀계 또는 폴리에스테르계의 재질인 웹형태의 접착제가 용융되어 형성된 것일 수 있으며, 웹형태의 접착제는 시트형상으로 그물형태방사한 것일 수 있다. 또한 접착층(30)은 저분자 섬유질을 포함할 수 있다.
접착층(30)에는 미세한 관통공이 형성되어 있어 제1담지체(10)와 제2담지체(20) 사이에서 화장료(40)가 이동할 수 있다.
제1실시예에 따르면 접착층(30)이 알코올에 안정한 성분이기 때문에, 알코올을 포함한 화장료(40)를 사용해도 제1담지체(10)와 제2담지체(20)의 접착이 안정적으로 이루어진다.
다른 실시예에서 담지체(1)의 형상은 사각판 등 다양하게 변형될 수 있으며, 3층 이상으로 구성될 수도 있다.
도 4는 본 발명의 제2실시예에 따른 담지체의 사시도이다.
접착층(30)은 산점분포되어 있으며, 이에 의해 제1접착면(11)과 제2접착면(21)은 부분적으로 접착되어 있다.
도 5는 본 발명의 제3실시예에 따른 담지체의 사시도이다.
접착층(30)에는 부분적으로 빈 부분이 형성되어 있으며, 이에 의해 제1접착면(11)과 제2접착면(21)은 부분적으로 접착되어 있다.
제2실시예 및 제3실시예에 따르면 제1담지체(10)와 제2담지체(20)는 서로 접착되어 있으면서도, 접착층(30)없이 직접 맞닿는 부분을 가지게 된다. 이에 의해 화장료(40)가 제1담지체(10)와 제2담지체(20) 사이에서 원활하게 이동할 수 있다.
이하에서는 본 발명에 따른 담지체의 제조방법을 설명한다.
도 6은 본 발명에 따른 담지체 제조방법의 일실시예를 나타낸 것이다.
제1담지체(10), 제2담지체(20) 및 접착시트(31)를 준비한다. 접착시트(31)는 폴리올레핀계 또는 폴리에스테르계 재질이며, 얇은 시트 형상을 가지고 있다. 접착시트(31)는 저온에서 용융되는 저분자의 섬유질을 그물형태방사한 부직포(nonwoven) 형태의 핫멜트 접착제일 수 있으며, 웹형태를 가지고 있을 수 있다. 접착시트(31)는 비교적 낮은 온도에서 접착성능을 나타낼 수 있으며, 예를 들어, 연화점(DSC softening point)이 105℃ 이하, 110℃ 이하 또는 120℃ 이하일 수 있으며, 더 구체적으로는 80℃ 내지 105℃, 80℃ 내지 110℃ 또는 80℃ 내지 120℃일 수 있다.
제1담지체(10)와 제2담지체(20) 사이에 접착시트(31)를 위치시키고, 접착시트(31)를 용융한다. 용융은 열풍을 이용하여 수행할 수 있으며, 접착시트(31)가 용융되면서 접착이 이루어진다. 접착시트(31)는 용융되어 접착층(30)을 형성하고 제1담지체(10)와 제2담지체(20)를 접착시킨다.
제1담지체(10)와 제2담지체(20)를 접착한 이후 화장료를 담지시킨다.
접착을 확실히 하기 위해 용융 중 또는 용융 후에 프레스 과정을 거칠 수 있다.
접착시트(31)를 이용한 접착은 전기퓨징프레스(electric fusing press), 가열된 롤, 열풍, 방사열 또는 스팀 프레스 등을 이용하여 수행될 수 있다. 열접착온도는 105℃ 내지 125℃일 수 있다.
도 7은 본 발명에 따른 담지체 제조방법의 다른 실시예를 나타낸 것이다.
제2담지체(20) 상에 접착시트(31)를 위치시키고 용융시켜 접착층(30)을 형성한다. 접착층(30)이 굳기 전에 제1담지체(10)를 접착층(30) 상에 위치시키고 제1담지체(10)와 제2담지체(20)를 접착시킨다.
이상 설명한 제조방법은 다양하게 변화할 수 있다. 접착시트(31)의 형태 및 분포는 다양하게 변화할 수 있으며, 이에 의해 접착층(30)의 형태도 달라진다. 또한, 접착시트(31)를 사용하지 않고 구상의 접착제나 액상의 접착제 등 다양한 다양한 형태의 접착제를 사용하여 접착층(30)을 형성할 수 있다.
이하 실험예를 통해 본 발명을 더욱 상세히 설명한다.
제1담지체(10)로 두께 1mm의 폴리우레탄 폼을 사용하였다. 폴리우레탄 폼은 폴리에테르와 폴리에스테르가 5:5이며, 폴리카보네이트디올을 함유하여 내화학성이 강화된 습식우레탄 폼이다.
제2담지체(20)로는 두께 8mm의 폴리에테르계 폴리우레탄 폼을 사용하였다
실시예에서 접착층(30)은 폴리에스테르계 저온 반응성 접착시트(31)를 이용하여 형성하였다. 비교예로는 이소시아네이트계 접착제를 사용하였다.
접착층(30)은 제1접착면(11)과 제2접착면(21) 전체에 걸쳐 형성되었으며, 열풍을 이용하여 접착시트(31)를 용융하였다. 용융 후 프레스, 세척 및 건조 과정을 거쳤다.
담지체 제조 후 알코올에 대한 분리강도를 테스트하였다. 사용된 알코올 용액은 에탄올 100%, 에탄올 15%, 에탄올 10% 및 에탄올 5%의 총 4가지였다.
테스트에서는 1) 담지체를 50℃ 항온조에서 알코올 용액 내에 7일 방치한 후 2) 핀셋으로 분리여부 확인하였으며 3) 핀셋으로 분리되지 않은 경우에는 세척후 내용물이 90%이상 제거된 상태에서 분리강도 측정(푸쉬풀게이지로 측정, 상단면은 집게가위 또는 푸쉬풀 집게로 고정하여 당기고 하단면은 지그 또는 손으로 고정)하였으며 4) 푸쉬풀게이지로 0.4kg.f로 당겼을때 분리여부 확인하였다(푸쉬풀게이지의 속도는 10mm/sec).
실험결과는 다음 표 1과 같다.
EtOH 100% EtOH 15% EtOH 10% EtOH 5%
비교예 0 Kg.f 0.1 kg.f 0.1 kg.f 0.2 kg.f
실시예 0.4 Kg.f 0.4Kg.f 0.6Kg.f 0.8Kg.f
실험결과를 보면 비교예에서는 에탄올 100%에서는 핀셋으로 분리되었으며, 에탄올 함량이 낮은 경우 핀셋으로 분리되지는 않았지만 낮은 분리강도를 나타낸다.
반면, 실시예에서는 에탄올 100% 용액에서도 큰 분리강도를 보여주고 있어 담지체가 안정적으로 접착되어 있음을 보여주고 있다.
전술한 실시예들은 본 발명을 설명하기 위한 예시로서, 본 발명이 이에 한정되는 것은 아니다. 본 발명이 속하는 기술분야에서 통상의 지식을 가진 자라면 이로부터 다양하게 변형하여 본 발명을 실시하는 것이 가능할 것이므로, 본 발명의 기술적 보호범위는 첨부된 특허청구범위에 의해 정해져야 할 것이다.

Claims (11)

  1. 화장료를 담지하는 담지체에 있어서,
    제1접착면을 가지는 제1담지체;
    상기 제1접착면과 마주하는 제2접착면을 가지는 제2담지체; 및
    상기 제1담지체와 상기 제2담지체 사이에 위치하여 상기 제1접착면와 상기 제2접착면을 접착시키는 접착층을 포함하며,
    상기 접착층은 폴리올레핀계 재질 및 폴리에스테르계 재질 중 적어도 어느 하나로 이루어진 담지체.
  2. 제1항에 있어서,
    상기 제1담지체와 상기 제2담지체에 담지되어 있는 화장료를 더 포함하며,
    상기 화장료는 알코올 성분을 포함하고 있는 것을 특징으로 하는 담지체.
  3. 제2항에 있어서,
    상기 제1담지체와 상기 제2담지체는 폴리우레탄 발포체인 것을 특징으로 하는 담지체.
  4. 제3항에 있어서,
    상기 제1담지체와 상기 제2담지체는 폴리에테르계 폴리우레탄 발포체인 것을 특징으로 하는 담지체.
  5. 제2항에 있어서,
    상기 접착층은 상기 제1접착면 및 상기 제2접착면의 전면에 형성되어 있는 것을 특징으로 하는 담지체.
  6. 제2항에 있어서,
    상기 접착층은 상기 상기 제1접착면 및 상기 제2접착면에 부분적으로 형성되어 있는 것을 특징으로 하는 담지체.
  7. 제2항에 있어서,
    상기 접착층은 저분자 섬유질을 포함하는 것을 특징으로 하는 담지체.
  8. 화장료를 담지하는 담지체의 제조방법에 있어서,
    제1접착면을 가지는 제1담지체 및 제2접착면을 가지는 제2담지체를 마련하는 단계와;
    상기 제1접착면 및 상기 제2접착면 사이에 접착 시트를 위치시키는 단계와;
    상기 접착 시트를 용융시켜 상기 제1접착면과 상기 제2접착면을 접착시키는 접착층을 형성하는 단계를 포함하며,
    상기 접착시트는 폴리올레핀계 재질 및 폴리에스테르계 재질 중 적어도 어느 하나로 이루어진 담지체의 제조방법.
  9. 제8항에 있어서,
    상기 접착층 형성 후 화장료를 상기 제1담지체와 상기 제2담지체에 담지하는 단계를 더 포함하며,
    상기 화장료는 알코올 성분을 포함하고 있는 것을 특징으로 하는 담지체의 제조방법.
  10. 제9항에 있어서,
    상기 제1담지체와 상기 제2담지체는 폴리우레탄 발포체인 것을 특징으로 하는 담지체의 제조방법.
  11. 제9항에 있어서,
    상기 접착 시트는 저분자 섬유질을 포함하는 것을 특징으로 하는 담지체의 제조방법.
PCT/KR2018/001699 2017-02-15 2018-02-08 접착층을 포함하는 담지체 및 담지체의 제조방법 WO2018151460A1 (ko)

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US16/485,987 US20200061965A1 (en) 2017-02-15 2018-02-08 Support comprising adhesive layer and manufacturing method for support
JP2019543947A JP2020507413A (ja) 2017-02-15 2018-02-08 接着層を備える担持体及び担持体の製造方法
CN201880012256.0A CN110337251A (zh) 2017-02-15 2018-02-08 包含粘合层的载体和用于载体的制造方法

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KR10-2017-0020662 2017-02-15
KR1020170020662A KR20180094399A (ko) 2017-02-15 2017-02-15 접착층을 포함하는 담지체 및 담지체의 제조방법

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US20200061965A1 (en) 2020-02-27
JP2020507413A (ja) 2020-03-12

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