WO2015060226A1 - Gloss composition, method for producing same and cosmetic preparation - Google Patents

Gloss composition, method for producing same and cosmetic preparation Download PDF

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Publication number
WO2015060226A1
WO2015060226A1 PCT/JP2014/077783 JP2014077783W WO2015060226A1 WO 2015060226 A1 WO2015060226 A1 WO 2015060226A1 JP 2014077783 W JP2014077783 W JP 2014077783W WO 2015060226 A1 WO2015060226 A1 WO 2015060226A1
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Prior art keywords
component
mass
glossy
composition
ratio
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PCT/JP2014/077783
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French (fr)
Japanese (ja)
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成代 佐々木
加藤 大介
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ライオン株式会社
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Publication of WO2015060226A1 publication Critical patent/WO2015060226A1/en

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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00Preparations for care of the hair
    • A61Q5/02Preparations for cleaning the hair
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/34Alcohols
    • A61K8/342Alcohols having more than seven atoms in an unbroken chain
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/37Esters of carboxylic acids
    • A61K8/375Esters of carboxylic acids the alcohol moiety containing more than one hydroxy group
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/39Derivatives containing from 2 to 10 oxyalkylene groups
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q1/00Make-up preparations; Body powders; Preparations for removing make-up
    • A61Q1/02Preparations containing skin colorants, e.g. pigments
    • A61Q1/04Preparations containing skin colorants, e.g. pigments for lips
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin
    • A61Q19/10Washing or bathing preparations
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00Preparations for care of the hair
    • A61Q5/12Preparations containing hair conditioners

Definitions

  • the present invention relates to a gloss composition, a method for producing the same, and a cosmetic.
  • This application claims priority on October 21, 2013 based on Japanese Patent Application No. 2013-218275 for which it applied to Japan, and uses the content here.
  • a gloss composition is used to give a pearly luster, for example.
  • a gloss composition containing a fatty acid glycol ester, a surfactant, water and a crystallization additive is known (for example, Patent Document 1).
  • Cosmetics designed for the purpose have been proposed.
  • an anionic surfactant a silicone derivative having a specific average particle diameter, a melting point of 55 to 75 ° C., at least a part of the crystalline form exists, and the ratio of the short diameter to the long diameter is 0.75 or less.
  • a liquid detergent composition containing a pearlizing agent having a crystal form and a specific alcohol has been proposed (for example, Patent Document 2).
  • an object of the present invention is to provide a glossy composition that imparts a pearly luster to a cosmetic and can further enhance the smoothness of the cosmetic during rinsing and the texture to be treated.
  • the present inventors have used a glossy composition containing crystals having a minor axis / major axis ratio of less than 0.45, so that smoothness during rinsing in cosmetics and the texture of the object to be treated are obtained. As a result, the present invention has been found.
  • the mass ratio represented by the component (C) / the component (A) is 0.2 to 1.5, and the ratio represented by the minor axis / major axis of the crystal is 0.45.
  • a gloss composition that is less than.
  • R 1 represents a hydrocarbon group having 13 to 21 carbon atoms
  • R 2 represents an alkylene group having 2 to 4 carbon atoms
  • m represents an average number of repetitions of (R 2 O).
  • Y represents a hydrogen atom or R 3 CO—
  • R 3 represents a hydrocarbon group having 13 to 21 carbon atoms.
  • [4] The method for producing a glossy composition according to [1], wherein the components (A) to (D) are mixed at a melting point or higher of the component (A) to obtain a mixture; A crystallization step of circulating the mixture to the crystallization tank and the cooler and cooling the mixture to a temperature below the freezing point of the component (A) using a production apparatus in which a tank and a cooler are connected. A method for producing a gloss composition.
  • the present invention relates to the following.
  • the mass ratio represented by the component (C) / component (A) is 0.2 to 1.5;
  • the ratio represented by the minor axis / major axis of the crystal is less than 0.45.
  • the gloss composition Y—O— (R 2 O) m —CO—R 1 (I) (In the formula (I), R 1 represents a hydrocarbon group having 13 to 21 carbon atoms; R 2 represents an alkylene group having 2 to 4 carbon atoms; m represents an average number of repetitions of (R 2 O)) Y represents a hydrogen atom or R 3 CO—; R 3 represents a hydrocarbon group having 13 to 21 carbon atoms.) [2 ′] The gloss composition according to [1 ′], further comprising an aromatic carboxylic acid or a salt thereof (E). [3 ′] A cosmetic containing the gloss composition according to [1 ′] or [2 ′].
  • [4 ′] The method for producing a glossy composition according to [1 ′] using a production apparatus including a crystallization tank and a cooler, In the manufacturing apparatus, the crystallization tank and the cooler are connected,
  • the manufacturing method includes: A mixing step of mixing the components (A) to (D) above the melting point of the component (A) to obtain a mixture;
  • a method for producing a glossy composition comprising:
  • a pearl-like gloss is imparted to the cosmetic, and the smoothness of the cosmetic during rinsing and the texture of the treatment target can be further enhanced.
  • FIG. 1 It is a schematic diagram which shows an example of the manufacturing apparatus of the glossy composition used for manufacture of the glossy composition which is one Embodiment of this invention.
  • 2 is a photomicrograph of the gloss composition of Example 1-1.
  • 2 is a photomicrograph of the gloss composition of Example 1-11.
  • 2 is a photomicrograph of the gloss composition of Comparative Example 1-1.
  • the gloss composition according to an embodiment of the present invention includes a crystal (hereinafter referred to as gloss crystal) containing a fatty acid glycol ester (A) represented by the following general formula (I), a surfactant (B), A composition containing alcohol (C) having 8 to 22 carbon atoms and water (D), for example, a composition in which the glossy crystals are dispersed in water.
  • gloss crystal a crystal containing a fatty acid glycol ester (A) represented by the following general formula (I), a surfactant (B), A composition containing alcohol (C) having 8 to 22 carbon atoms and water (D), for example, a composition in which the glossy crystals are dispersed in water.
  • gloss composition in the present invention means a composition that imparts pearly luster to cosmetics and the like. Cosmetics include body shampoos, body shampoos, hand soaps, face soaps, and other body care products; hair rinses, body treatments and other body care products, and hair and skin after washing. And liquid preparations used for skin care.
  • R 1 represents a hydrocarbon group having 13 to 21 carbon atoms
  • R 2 represents an alkylene group having 2 to 4 carbon atoms
  • m represents an average number of repetitions of (R 2 O)
  • Y represents a hydrogen atom or R 3 CO—
  • R 3 represents a hydrocarbon group having 13 to 21 carbon atoms.
  • the glossy crystal has a minor axis / major axis ratio (hereinafter sometimes referred to as minor axis / major axis ratio) of less than 0.45, preferably a minor axis / major axis ratio of less than 0.35,
  • the major axis ratio is more preferably less than 0.30. If the ratio of the minor axis / major axis is less than the above upper limit, the smoothness at the time of rinsing in the cosmetic and the texture of the treatment object can be enhanced. This is thought to be because gloss crystals are entangled with each other and other components in the cosmetic (for example, silicone compounds and cationic polymers described later) are taken in and easily attached to the hair or skin to be treated. .
  • the glossy crystals are intertwined means a state in which the end portions are in contact with each other or the end portions and the side portions do not overlap on the side surfaces in the major axis direction.
  • the lower limit of the minor axis / major axis ratio of the glossy crystal is not particularly limited, but is substantially 0.10, and is preferably 0.20 from the viewpoint of production efficiency. That is, in the glossy crystal, the ratio expressed by the minor axis / major axis is preferably 0.10 or more and less than 0.45, more preferably 0.10 or more and less than 0.35, and more preferably 0.20 or more and 0.35. Is more preferably 0.20 or more and less than 0.30.
  • the minor axis / major axis ratio of the glossy crystals is determined by measuring the major axis and minor axis of any 10 glossy crystals using a microscope, and calculating the average value of the measured major axis and the average value of the minor axis, It is a value obtained by further calculating the minor axis / major axis from these calculated values (that is, the average value of the minor axis / major axis ratio).
  • the “major axis” of the glossy crystal means the maximum value in the size of the glossy crystal
  • the “minor axis” means the minimum value in the size of the glossy crystal.
  • the percentage of glossy crystals having a minor axis / major axis ratio of less than 0.45 among the glossy crystals contained in the glossy composition is the total number of glossy crystals contained in the glossy composition. On the other hand, it is preferably 50% (number conversion) or more, more preferably 75% or more, and may be 100%. If the long crystal ratio is equal to or higher than the lower limit, the smoothness of the rinsing feeling in the cosmetic and the texture of the treatment target can be further improved.
  • the long crystal ratio is obtained by diluting the obtained dispersion 20 times with ion-exchanged water, photographing with 5 or more fields of view with a microscope, and arbitrarily measuring the short and long diameters of 50 crystals from each field. Can do.
  • the size of the glossy crystal is not particularly limited.
  • the major axis is preferably 0.8 ⁇ m or more, more preferably 1.5 ⁇ m or more, and further preferably 2.0 ⁇ m or more. If it is less than the said lower limit, it will become difficult to intertwine glossy crystals, and there exists a possibility that the smoothness at the time of a rinse in cosmetics and the texture of a process target may fall.
  • the upper limit value of the major axis is not particularly limited, and is preferably 4.0 ⁇ m, for example, and more preferably 3.0 ⁇ m. Above the upper limit, the size of the tangled glossy crystals becomes too large and stickiness tends to occur.
  • the major axis of the glossy crystal is preferably 0.8 ⁇ m or more and 4.0 ⁇ m or less, more preferably 1.5 ⁇ m or more and 4.0 ⁇ m or less, further preferably 2.0 ⁇ m or more and 4.0 ⁇ m or less, and 2.0 ⁇ m or more. 3.0 ⁇ m or less is particularly preferable.
  • the minor axis of the glossy crystal is not particularly limited, but is preferably 0.3 ⁇ m or more, and more preferably 0.4 ⁇ m or more. If it is less than the said lower limit, it will become easy to crush at the time of a rinse.
  • the upper limit of the minor axis is not particularly limited, and is preferably 1.2 ⁇ m or less, and more preferably 1.0 ⁇ m or less.
  • the minor axis of the glossy crystal is preferably 0.3 ⁇ m or more and 1.2 ⁇ m or less, more preferably 0.4 ⁇ m or more and 1.2 ⁇ m or less, further preferably 0.3 ⁇ m or more and 1.0 ⁇ m or less, and 0.4 ⁇ m.
  • 1.0 micrometer or less is especially preferable.
  • the viscosity of the gloss composition is not particularly limited, and is preferably 50 to 200 mPa ⁇ s, for example.
  • the viscosity of the gloss composition is a value read 60 seconds after the start of rotor rotation using a BL type viscometer (rotor: No. 3, rotation speed: 60 rpm, measurement temperature: 25 ° C., manufactured by Toki Sangyo Co., Ltd.). is there.
  • the viscosity is defined as a value at 25 ° C. unless otherwise specified. That is, even if the value is outside the range specified in the present specification, it is included in the scope of the present invention as long as it is a viscosity value within the range specified in the present specification when corrected to a value at 25 ° C.
  • the fatty acid glycol ester (A) (hereinafter sometimes referred to as the component (A)) is represented by the following general formula (I). Y—O— (R 2 O) m —CO—R 1 (I)
  • R 1 represents a hydrocarbon group having 13 to 21 carbon atoms.
  • R 1 may have an unsaturated bond or may not have an unsaturated bond.
  • R 1 is preferably an alkyl group or an alkenyl group.
  • R 1 may be a straight chain or a branched chain.
  • R 1 has 13 to 21 carbon atoms, preferably 16 to 20 carbon atoms. If the number of carbon atoms is less than the lower limit, the melting point is low and unstable, and if it exceeds the upper limit, the melting point and the solidification temperature increase, resulting in a decrease in production efficiency.
  • R 1 is preferably, for example, a pentadecyl group, a heptadecyl group, a heneicosyl group, or the like.
  • Y represents a hydrogen atom or R 3 CO—.
  • the component (A) is a mono fatty acid ester
  • the component (A) is a di fatty acid ester.
  • Y is, when an R 3 CO-, as the R 3, include the same groups as R 1.
  • R 3 may be the same group as R 1 or a different group.
  • R 2 represents an alkylene group having 2 to 4 carbon atoms. That is, (R 2 O) is an oxyalkylene group having 2 to 4 carbon atoms.
  • R 2 preferably has 2 to 3 carbon atoms. If the carbon number of R 2 is within the above range, crystallization is easy.
  • m represents the average number of repetitions of (R 2 O) and is a number of 1 to 3, more preferably 1 to 2. Note that m may be an integer or may include a decimal.
  • the average number of repetitions of (R 2 O) means the average number of moles of R 2 O added to 1 mole of the fatty acid ester used. If m is in the above range, it becomes water-insoluble and stable glossy crystals can be obtained even in the presence of the surfactant (B).
  • the melting point of the component (A) is preferably 50 ° C. or higher, more preferably 50 to 90 ° C., and further preferably 60 to 80 ° C. If the amount is less than the lower limit, the stability of the glossy crystals in the presence of the surfactant (B) may be lowered. If the amount exceeds the upper limit, the melting point is high, so that the surfactant (B ) May decrease in stability.
  • the freezing point of component (A) is preferably less than 80 ° C, more preferably 40 to 70 ° C.
  • component (A) monoethylene glycol form of mono fatty acid ester such as ethylene glycol monopalmitate, ethylene glycol monostearate, ethylene glycol monoisostearate; ethylene glycol dipalmitate, ethylene glycol distearate, ethylene glycol dibehenate Mono-fatty acid ester monoethylene glycol bodies; mono-fatty acid esters or di-fatty acid ester diethylene glycol bodies; mono-fatty acid esters or di-fatty acid ester triethylene glycol bodies, and the like.
  • a monoethylene glycol body is preferable, a monoethylene glycol body of a difatty acid ester is more preferable, and ethylene glycol distearate is further preferable.
  • These (A) components may be used individually by 1 type, and may be used in combination of 2 or more type.
  • the lower limit of the content of the component (A) in the gloss composition is preferably 2% by mass, more preferably 3% by mass, and still more preferably 4% by mass with respect to the total mass of the gloss composition.
  • the upper limit of the content of the component (A) in the gloss composition is preferably 10% by mass, more preferably 7% by mass, and still more preferably 6% by mass with respect to the total mass of the gloss composition. That is, the content of the component (A) in the gloss composition is preferably 2% by mass or more and 10% by mass or less, more preferably 3% by mass or more and 7% by mass or less with respect to the total mass of the gloss composition. 4 mass% or more and 6 mass% or less are more preferable.
  • content of (A) component here means the total amount of (A) component which is a crystalline state, and (A) component which is not a crystalline state in a glossy composition. If it is less than the said lower limit, in order to provide sufficient gloss to cosmetics, there exists a possibility that the compounding quantity of a glossy composition must be raised too much. If it exceeds the upper limit, the fluidity may be impaired and handling may be complicated.
  • the gloss composition contains a surfactant (B) (hereinafter sometimes referred to as component (B)).
  • the component (B) can increase the dispersibility of the component (A) in the dispersion medium and reduce the minor axis / major axis ratio of the glossy crystal in the method for producing a gloss composition described later.
  • Examples of the component (B) include anionic surfactants, nonionic surfactants, and amphoteric surfactants.
  • anionic surfactant examples include higher fatty acid salts having 8 to 22 carbon atoms, polyoxyethylene alkyl ether sulfate, ⁇ -olefin sulfonate, alkyl sulfonate, alkyl sulfate, N-acyl glutamate and the like.
  • the counter ion of the anionic surfactant include alkali metal ions, alkaline earth metal ions, ammonium ions, alkanolamines having 1 to 3 alkanol groups having 2 or 3 carbon atoms, and the like.
  • nonionic surfactant examples include lauric acid monoethanolamide, coconut oil fatty acid diethanolamide, polyoxyethylene alkylphenyl ether, polyoxyethylene alkyl ether, and polyoxyethylene lauric acid monoethanolamide.
  • amphoteric surfactant examples include alkyl dimethyl carboxymethyl ammonium betaine, alkyl carboxymethyl imidazolium betaine, N- (N′-acylaminoalkyl) -N-hydroxyalkylaminocarboxylate and the like.
  • an anionic surfactant is preferable from the viewpoint of enhancing the dispersibility of the component (A) in the component (D), polyoxyethylene alkyl ether sulfate is more preferable, and 1 to 5 mol of ethylene oxide is used.
  • the ammonium salt or sodium salt of polyoxyethylene alkyl ether sulfate having an added alkyl group having 12 to 14 carbon atoms is more preferable.
  • the lower limit of the content of the component (B) in the gloss composition is preferably 5% by mass and more preferably 10% by mass with respect to the total mass of the gloss composition.
  • the upper limit of the content of the component (B) in the gloss composition is preferably 30% by mass and more preferably 20% by mass with respect to the total mass of the gloss composition. That is, the content of the component (B) in the gloss composition is preferably 5% by mass or more and 30% by mass or less, and more preferably 10% by mass or more and 20% by mass or less with respect to the total mass of the gloss composition. . If the ratio is less than the lower limit, it is difficult to reduce the minor axis / major axis ratio of the glossy crystal. If the ratio exceeds the upper limit, the fluidity is impaired and handling may be complicated.
  • the mass ratio represented by component (A) / component (B) (hereinafter sometimes referred to as A / B ratio) is preferably 0.1 to 0.5, preferably 0.2 to 0.00. 4 is more preferable. If it is more than the said lower limit, a glossy crystal can be easily precipitated in the crystallization process mentioned later, and if it is below the said upper limit, it will be easy to obtain a fine glossy crystal.
  • the gloss composition contains an alcohol (C) having 8 to 22 carbon atoms (hereinafter sometimes referred to as component (C)).
  • component (C) an alcohol having 8 to 22 carbon atoms
  • the dispersibility of the component (A) in the component (D) is increased, and fine gloss crystals having a smaller minor axis / major axis ratio are obtained. can get.
  • the component (C) may be a saturated aliphatic alcohol or an unsaturated aliphatic alcohol.
  • the hydrocarbon group in component (C) may be linear or branched.
  • the component (C) is preferably an aliphatic alcohol having 12 to 22 carbon atoms such as lauryl alcohol, myristyl alcohol, cetyl alcohol, stearyl alcohol, behenyl alcohol, lauryl alcohol, myristyl alcohol, Aliphatic alcohols having 12 to 18 carbon atoms such as cetyl alcohol and stearyl alcohol are more preferred.
  • cetyl alcohol and stearyl alcohol are preferred from the viewpoint of reducing the minor axis / major axis ratio of the glossy crystal.
  • These (C) components may be used alone or in combination of two or more.
  • the lower limit of the content of the component (C) in the gloss composition is preferably 1% by mass, more preferably 2% by mass, and still more preferably 3% by mass with respect to the total mass of the gloss composition.
  • the upper limit of the content of the component (C) in the gloss composition is preferably 10% by mass, more preferably 6% by mass, and still more preferably 4% by mass with respect to the total mass of the gloss composition. That is, the content of the component (C) in the gloss composition is preferably 1% by mass or more and 10% by mass or less, more preferably 2% by mass or more and 6% by mass or less, and more preferably 3% by mass or more and 4% by mass or less. Is more preferable. If it is more than the said lower limit, the breadth / major axis ratio of a glossy crystal can be made smaller, and if it is below the said upper limit, it will be easy to suppress the sticky feeling of a process target.
  • the mass ratio represented by component (C) / component (A) (hereinafter sometimes referred to as C / A ratio) is 0.2 to 1.5.
  • the lower limit value of the C / A ratio is preferably 0.4, and more preferably 0.6.
  • the upper limit value of the C / A ratio is preferably 1.3, and more preferably 1.0. That is, in the glossy composition, the mass ratio represented by the component (C) / component (A) is preferably 0.4 or more and 1.3 or less, and more preferably 0.6 or more and 1.0 or less. If the C / A ratio is not less than the above lower limit, the minor / major axis ratio of the glossy crystal can be further reduced. If it is below the upper limit, the minor axis / major axis ratio of the glossy crystal can be made smaller, and the stickiness of the object to be treated can be easily suppressed.
  • the mass ratio represented by component (B) / component (C) (hereinafter sometimes referred to as B / C ratio) is preferably from 2 to 10, and more preferably from 4 to 8. If it is more than the said lower limit, (C) component will become easy to melt
  • the glossy composition contains water (D) (hereinafter sometimes referred to as component (D)).
  • the component (D) mainly serves as a dispersion medium for the gloss composition.
  • the content of water in the gloss composition is preferably 25 to 90% by mass, more preferably 40 to 90% by mass, and still more preferably 50 to 80% by mass with respect to the total mass of the gloss composition. If the amount is less than the above lower limit value, the fluidity may be impaired and handling may be complicated. If the amount exceeds the upper limit value, the amount of the gloss composition is excessively increased in order to impart sufficient gloss to the cosmetic. It may be necessary.
  • the gloss composition may contain an aromatic carboxylic acid or a salt thereof (E) (hereinafter sometimes referred to as component (E)).
  • component (E) makes it easy to obtain glossy crystals having a smaller minor axis / major axis ratio in the method for producing a glossy composition described later. The reason why the glossy crystal becomes longer and the minor axis / major axis ratio becomes smaller by containing the component (E) is not clear, but is presumed as follows.
  • the component (E) acts on the emulsified particles obtained by emulsifying the components (A) to (C), and increases the solubility of the emulsified particles in the component (D). For this reason, the supersaturation degree of the whole mixture becomes low, and excessive precipitation of glossy crystal nuclei is suppressed. When the number of glossy crystal nuclei precipitated is reduced, aggregation of fine crystals is suppressed, and it is considered that it is easy to grow into a long glossy crystal.
  • benzoic acid, phthalic acid, terephthalic acid, isophthalic acid, salicylic acid or a salt thereof is preferable.
  • the salt alkali metal salts, alkaline earth metal salts, ammonium salts, and alkanolamine salts are preferable.
  • the content of the component (E) in the gloss composition is preferably 0.2 to 3% by mass and more preferably 0.5 to 1.5% by mass with respect to the total mass of the gloss composition. If it is less than the lower limit, it is difficult to obtain the effect of the component (E), and if it exceeds the upper limit, gloss crystals are hardly formed.
  • the mass ratio represented by component (A) / component (E) (hereinafter sometimes referred to as A / E ratio) is preferably 1 to 10, and more preferably 3 to 6. If it is at least the above lower limit value, it is easy to make the minor axis / major axis ratio of the glossy crystal smaller, and if it is at most the above upper limit value, it is easy to suppress the formation of coarse crystals.
  • the mass ratio represented by component (B) / component (E) (hereinafter sometimes referred to as B / E ratio) is preferably 5 to 60, and more preferably 10 to 30. If the B / E ratio is within the above range, it is easy to make the minor axis / major axis ratio of the glossy crystal smaller.
  • the gloss composition is a pH adjuster, a monovalent alcohol (arbitrary alcohol) other than the component (C), polyol, preservative, salts and other optional components (for gloss composition) Optional components).
  • the pH adjuster include triethanolamine and citric acid.
  • the glossy composition preferably has a pH of 4.5 to 6.0.
  • the method for producing a gloss composition comprises a mixing step of mixing the components (A) to (D) at a melting point or higher of the component (A) to obtain a mixture, and the mixture as a crystallization tank.
  • FIG. 1 is a schematic diagram showing an example of a glossy composition production apparatus (hereinafter sometimes simply referred to as production apparatus) according to an embodiment of the present invention.
  • the manufacturing apparatus 1 in FIG. 1 includes a crystallizer 10 and a cooler 20.
  • the crystallizer 10 and the cooler 20 are connected by a first pipe 22 and a second pipe 26, and a pump 24 is provided in the first pipe 22.
  • the crystallizer 10 includes a crystallization tank 12 and a stirring blade 14 provided in the crystallization tank 12.
  • the crystallization tank 12 may be any crystallization tank whose inside can be adjusted to an arbitrary temperature, and examples thereof include a jacketed container.
  • Examples of the cooler 20 include a spiral heat exchanger, which is a liquid-liquid heat exchanger, a plate heat exchanger, a double tube heat exchanger, a multi-tube cylindrical heat exchanger, and a multi-tube heat Air-cooled type that is a heat exchanger, spiral tube heat exchanger, spiral plate heat exchanger, tank coil heat exchanger, tank jacket heat exchanger, direct contact liquid-liquid heat exchanger, gas-liquid heat exchanger A heat exchanger, a direct contact gas-liquid heat exchanger, a fin tube heat exchanger, etc.
  • the pump 24 includes a turbo pump such as a spiral pump, a turbine pump, an axial pump, and a mixed flow pump; a constant capacity pump such as a gear pump, a direct acting steam pump, a plunger pump, and a piston pump; a jet pump, an air lift pump, Special pumps such as water hammer pumps and diaphragm pumps are listed.
  • components (A) to (D) and, if necessary, optional components for the gloss composition (component (E), pH adjuster, monovalent alcohol (optional alcohol) other than component (C), polyol, (At least one component selected from the group consisting of preservatives and salts) is charged into the crystallization tank 12 and stirred to obtain a mixture 30 while being heated to a temperature equal to or higher than the melting point of the component (A) (mixing step). ).
  • the order of mixing the components in the mixing step is not particularly limited.
  • all the components used for the production of the gloss composition are charged into the crystallization tank 12 and heated to a temperature equal to or higher than the melting point of the component (A).
  • the components may be mixed (collective mixing method) while mixing, or the components may be mixed (split mixing method) while being sequentially introduced into the crystallization tank 12.
  • split mixing method arbitrary components among the components used for the production of the gloss composition are mixed (first mixing operation), and then the remaining components not used in the first mixing operation are mixed. (Second mixing operation) method may be mentioned.
  • the component (B) and the component (D) may be mixed, or the component (A), the component (B), and the component (D) may be mixed.
  • the first mixing operation is carried out by adding the component (B), the component (C), and the component (D) above the melting point of the component (C). It is preferable to mix at a temperature. That is, as the split mixing method, the component (B), the component (C), and the component (D) are mixed at a temperature equal to or higher than the melting point of the component (C), and then the second mixing operation is performed.
  • the component (A) it is preferable to add the component (A) to the primary mixture obtained by the first mixing operation at a temperature equal to or higher than the melting point of the component (A) and to mix at a temperature equal to or higher than the melting point of the component (A).
  • the (B) component, the (C) component, and the (D) component in the first mixing operation in the second mixing operation, the (A) component is previously melted at a temperature equal to or higher than the melting point of the (A) component.
  • this is added to the primary mixture of the component (B), the component (C), and the component (D) obtained by the first mixing operation, and mixed at a temperature equal to or higher than the melting point of the component (A). Is preferred.
  • the addition timing of the optional component for the gloss composition is determined in consideration of the type of the optional component for the gloss composition.
  • the component (E) is preferably mixed in the first mixing operation.
  • a glossy crystal can be made longer because a component is mixed by 1st mixing operation. That is, when the component (E) is used as an optional component for the gloss composition, the first mixing operation mixes the component (B), the component (C), the component (D), and the component (E), Subsequently, it is preferable to add and mix (A) component to the primary mixture obtained by said 1st mixing operation by 2nd mixing operation.
  • the first mixing operation includes the component (B), the component (C), the component (D), and the component (E). Then, in the second mixing operation, the components (A) and optional components other than the component (E) are melt-mixed, and this is added to the primary mixture obtained in the first mixing operation. It is preferable to mix.
  • the blending amount of component (A) in the mixing step is based on the total mass of the mixture in which all the components used for producing the gloss composition are mixed (that is, the total amount of all the components used for producing the gloss composition).
  • the content is preferably 2 to 10% by mass, more preferably 3 to 7% by mass, and still more preferably 4 to 6% by mass. If the amount is less than the lower limit, the content of the glossy crystal in the glossy composition is too small, and the blending amount of the glossy composition may have to be excessively increased in order to impart sufficient gloss to the cosmetic. is there. If it exceeds the upper limit, the fluidity may be impaired and handling may be complicated.
  • the blending amount of component (B) in the mixing step is based on the total mass of the mixture in which all the components used for producing the gloss composition are mixed (that is, the total amount of all the components used for producing the gloss composition). 5 to 30% by mass is preferable, and 10 to 20% by mass is more preferable. If the ratio is less than the lower limit, it is difficult to reduce the minor axis / major axis ratio of the glossy crystal. If the ratio exceeds the upper limit, the fluidity is impaired and handling may be complicated.
  • the blending amount of component (C) in the mixing step is based on the total mass of the mixture in which all the components used for producing the gloss composition are mixed (that is, the total amount of all the components used for producing the gloss composition). 1 to 10% by mass is preferable, and 2 to 6% by mass is more preferable. If it is more than the said lower limit, the breadth / major axis ratio of a glossy crystal can be made smaller, and if it is below the said upper limit, it will be easy to suppress the sticky feeling of a process target.
  • the blending amount of component (D) in the mixing step is based on the total mass of the mixture in which all components used for producing the gloss composition are mixed (that is, the total amount of all components used for producing the gloss composition).
  • the content is preferably 25 to 90% by mass, more preferably 40 to 90% by mass, and still more preferably 50 to 80% by mass. If the amount is less than the above lower limit value, the fluidity may be impaired and handling may be complicated. If the amount exceeds the upper limit value, the amount of the gloss composition is excessively increased in order to impart sufficient gloss to the cosmetic. It may be necessary.
  • the blending amount of the component (E) in the mixing step is the total mass of the mixture in which all the components used for the production of the gloss composition are mixed (that is, the gloss).
  • the total amount of all components used in the production of the composition is preferably 0.2 to 3% by mass, more preferably 0.5 to 1.5% by mass. If it is less than the lower limit, it is difficult to obtain the effect of the component (E), and if it exceeds the upper limit, gloss crystals are hardly formed.
  • the A / B ratio in the mixing step is preferably from 0.1 to 0.5, more preferably from 0.2 to 0.4. If it is more than the said lower limit, a glossy crystal can be easily precipitated in the crystallization process mentioned later, and if it is below the said upper limit, it will be easy to obtain a fine glossy crystal.
  • the C / A ratio in the mixing step is 0.2 to 1.5.
  • the lower limit value of the C / A ratio is preferably 0.4, and more preferably 0.6.
  • the upper limit value of the C / A ratio is preferably 1.3, and more preferably 1.0. That is, the C / A ratio is preferably 0.4 or more and 1.3 or less, and more preferably 0.6 or more and 1.0 or less.
  • the minor / major axis ratio of the glossy crystal can be further reduced. If it is below the upper limit, it is easy to control the precipitation of crystals in the crystallization step, and the minor axis / major axis ratio of the glossy crystals can be made smaller.
  • the B / C ratio in the mixing step is preferably from 2 to 10, and more preferably from 4 to 8. If the B / C ratio is equal to or higher than the lower limit, the component (C) is easily dissolved and a glossy crystal can be easily produced. If the B / C ratio is equal to or lower than the upper limit, the minor axis / major axis ratio of the glossy crystal can be further reduced. .
  • the A / E ratio in the mixing step is preferably 1 to 10, and more preferably 3 to 6. If the A / E ratio is not less than the above lower limit value, the minor axis / major axis ratio of the glossy crystal can be made smaller, and if it is not more than the above upper limit value, the formation of coarse crystals can be easily suppressed.
  • the B / E ratio in the mixing step is preferably 5 to 60, and more preferably 10 to 30. If the B / E ratio is within the above range, it is easy to make the minor axis / major axis ratio of the glossy crystal smaller.
  • the temperature in the mixing step is equal to or higher than the melting point of the component (A), preferably 1 to 30 ° C. higher than the melting point of the component (A), and 1 to 20 ° C. higher than the melting point of the component (A). Temperature is more preferred. If the ratio is less than the lower limit, the ratio of the minor axis / major axis of the glossy crystal may be large and coarse, and if the ratio exceeds the upper limit, the cooling time may be long and the production efficiency may be reduced.
  • the mixing temperature is preferably a temperature at which the components (A) to (C) can be melted.
  • the mixing temperature is preferably 75 to 90 ° C, more preferably 75 to 85 ° C.
  • the mixing step is preferably performed under weak stirring conditions.
  • n 3 d 5 / V n represents the rotation speed (rpm) of the stirring blade.
  • d indicates the blade diameter (m) of the stirring blade (corresponding to d1 in FIG. 1).
  • the “blade diameter of the stirring blade” here refers to the stirring blade when the crystallization tank is viewed from directly above.
  • the diameter in the circumscribed circle. V represents the volume (m 3 ) of the mixed solution.
  • the stirring blade 14 may be operated continuously or intermittently.
  • the “intermittent operation” includes an operation in which the mixing is stopped and then restarted again, for example, when defoaming occurs when foaming is severe.
  • one aspect of the mixing step according to the method for producing a glossy composition which is an embodiment of the present invention is: Components (A) to (D), and optionally, optional components for gloss compositions (component (E), pH adjuster, monohydric alcohol (arbitrary alcohol) other than component (C)), polyols, preservatives, salts At least one component selected from the group consisting of: a crystallization tank and stirring while heating at the mixing temperature to obtain a mixture;
  • the mixing step includes All of the components are charged into the crystallization tank and mixed by a batch mixing method in which the components are mixed while heating to the mixing temperature, or at the mixing temperature while all of the components are sequentially added to the crystallization tank.
  • the split mixing method is: A first mixing operation of mixing a component (B), a component (C), a component (D), and optionally a component (E) to obtain a primary mixture; And a second mixing operation of adding and mixing the component (A) and an optional component other than the component (E) as required to the primary mixture.
  • the mixing temperature is preferably equal to or higher than the melting point of the component (A).
  • the pump 24 is started.
  • the mixture 30 in the crystallization tank 12 enters the cooler 20 via the first pipe 22.
  • the mixture 30 that has entered the cooler 20 flows through the cooler 20 and is cooled.
  • the mixture 30 circulated through the cooler 20 returns to the crystallization tank 12 via the second pipe 26.
  • the mixture 30 in the crystallization tank 12 circulates between the crystallization tank 12 and the cooler 20 (crystallization process).
  • a part of the mixture 30 in the crystallization tank 12 is continuously extracted, cooled by the cooler 20, and returned to the crystallization tank 12, thereby precipitating a glossy crystal and the gloss composition of the present invention. obtain.
  • the cooling temperature in the cooler 20 (that is, the temperature of the cooler (refrigerant)) is a temperature not higher than the freezing point of the component (A), preferably 5 to 20 ° C. lower than the freezing point of the component (A).
  • the temperature is preferably 5 to 15 ° C. lower than the freezing point of the component.
  • Examples of the cooling temperature in the cooler 20 include 10 to 40 ° C. If the ratio is less than the above lower limit, the minor axis / major axis ratio of the glossy crystals is unlikely to be small, and if the ratio exceeds the upper limit, fine aggregates of glossy crystals may be generated.
  • the cooling temperature in the cooler 20 can be adjusted by setting the temperature of the refrigerant within the above range.
  • the cooling rate in the cooler 20 is not particularly limited.
  • the cooling rate is preferably a condition for lowering the mixture 30 in the crystallization tank 12 at 0.1 to 20 ° C./min, and a condition for lowering the mixture 30 in the crystallization tank 12 at 0.1 to 10 ° C./min. More preferably, the conditions for lowering the mixture 30 in the crystallization tank 12 at 0.1 to 5 ° C./min are more preferable. Since the crystallization can be performed in a short time if the above lower limit is exceeded, the production efficiency of the glossy composition can be improved. Of less than 0.45.
  • the circulation speed of the mixture 30 in the crystallization step is determined in consideration of the amount of the mixture 30 in the crystallization tank 12, the cooling temperature in the cooler 20, and the like. For example, it is preferable that 0.01 to 0.5 times the amount of the mixture 30 per minute be passed through the cooler 20 and returned to the crystallization tank 12.
  • the time of the crystallization process is not particularly limited, and the time when the mixture 30 in the crystallization tank 12 reaches the crystallization end temperature is defined as the end point of the crystallization process.
  • the crystallization end temperature is not particularly limited, and may be any temperature below the freezing point of component (A), more preferably 5 to 40 ° C. lower than the freezing point of component (A), and 10 times higher than the freezing point of component (A). A temperature of ⁇ 35 ° C. is more preferred.
  • the crystallization end temperature is preferably, for example, 10 to 45 ° C, more preferably 30 to 40 ° C.
  • the mixture 30 cooled by the cooler 20 is returned to the crystallization tank 12, and the temperature of the mixture 30 in the crystallization tank 12 decreases.
  • the time required for the temperature of the mixture 30 in the crystallization tank to fall below the melting point of the component (A) and below the freezing point is preferably 5 to 30 minutes, more preferably 10 to 20 minutes. If it is in the above-mentioned range, it is easy to obtain a glossy crystal that is fine and has a smaller minor axis / major axis ratio.
  • An aging step may be provided after the crystallization step.
  • the glossy crystal can be further elongated, and the minor axis / major axis ratio of the glossy crystal can be further reduced.
  • the aging step is a step of maintaining the gloss composition at a temperature of 30 to 60 ° C. for 2 to 24 hours, for example.
  • a method of circulating the glossy composition in the crystallization tank 12 to the cooler 20 in the same manner as the crystallization process a method of stopping the pump 24 and maintaining the inside of the crystallization tank 12 at an arbitrary temperature.
  • a method of putting the glossy composition in the crystallization tank 12 in another container and maintaining the container at an arbitrary temperature can be mentioned.
  • the glossy composition may or may not be stirred. However, from the viewpoint of preventing the lustrous crystals from being crushed, it is preferable not to stir.
  • the temperature of the aging step (aging temperature) is determined in consideration of the type of the component (A) and the like, and is below the melting point.
  • the aging temperature is preferably 30 to 60 ° C., for example. If the aging temperature is not less than the above lower limit value, the growth time of the glossy crystal can be further shortened. .
  • the time of the ripening step (ripening time) is determined in consideration of the desired minor diameter / major diameter ratio of the glossy crystal and is preferably, for example, 2 to 24 hours. If the aging time is equal to or greater than the above lower limit value, the glossy crystal can be elongated to make the minor axis / major axis ratio of the glossy crystal smaller. And is less likely to be crushed.
  • the mixing step is performed by the crystallizer 10.
  • the present invention is not limited to this, and the mixture 30 is prepared by an apparatus other than the crystallizer 10, and the mixture 30 is crystallized. You may throw into the tank 12.
  • one aspect of the crystallization process according to the method for producing a glossy composition which is an embodiment of the present invention is a crystallization process in which the mixture obtained in the mixing process is circulated between a crystallization tank and a cooler for cooling. Is;
  • the cooling temperature in the cooler is 5 to 20 ° C. lower than the freezing point of the component (A),
  • the cooling rate of the mixture in the crystallization tank is 0.1-20 ° C./min;
  • the circulation speed in the circulation is a speed at which 0.01 to 0.5 times the amount of the mixture in the crystallization tank per 1 minute is passed through the cooler and returned to the crystallization tank.
  • the time of the said crystallization process is a crystallization process which is until the mixture in the said crystallization tank reaches the crystallization completion temperature.
  • the crystallization step time is preferably 5 to 30 minutes, and the crystallization end temperature is preferably 5 to 40 ° C. lower than the freezing point of the component (A).
  • One aspect of the manufacturing method of the glossy composition which is one embodiment of the present invention is: A mixing step in which the components (A) to (D) are mixed at a melting point or higher of the component (A) to obtain a mixture, a crystallization step in which the mixture is circulated through a crystallization tank and a cooler, and a ripening step; ,including.
  • the aging temperature is preferably 30 to 60 ° C.
  • the aging time is preferably 2 to 24 hours.
  • the sample is transferred from the crystallization tank to a transfer aging tank or storage tank.
  • a transfer method a method of utilizing gravity by setting the transfer destination to a low ground or a pump is used.
  • a pump having a relatively low shear a rotary pump, a Mono pump, a gear pump, a sine pump, etc.
  • the crystal is not crushed and the ratio of the short axis / long axis is not increased.
  • filtration is performed to remove foreign substances that are harmful to the control of crystal agglomeration and short / long diameter ratio control.
  • a vessel As the opening of the filter, it is preferable to select the smallest one in consideration of productivity within a range of 300 ⁇ m or less.
  • a device capable of heating and cooling is selected as necessary. It is added and mixed from the storage tank to the final product, and in that case, using the same pump as the above transfer method, it is added to the upper surface of the blending tank or in the liquid, When the difference in viscosity is large, the mixing efficiency can be improved by using means such as adding to the inlet side of a centrifugal pump or the like. It is preferable to use the above-described pump and filtration device for transfer from the final product blending tank to the product storage tank.
  • the cosmetic which is one embodiment of the present invention contains a gloss composition.
  • the content of the gloss composition in the cosmetic is not particularly limited, but is preferably 10 to 50% by mass, more preferably 20 to 40% by mass, and more preferably 30 to 40% by mass with respect to the total mass of the cosmetic. Is more preferable. If it is less than the lower limit, the gloss of the cosmetic may be lowered, and if it exceeds the upper limit, the function of the cosmetic such as a cleaning power or a texture to be treated may be lowered.
  • the cosmetic may contain a silicone compound (F), a cationic polymer (G) and the like in addition to the gloss composition. That is, one aspect of the cosmetic according to an embodiment of the present invention includes the gloss composition, A cosmetic comprising a silicone compound (F), a cationic polymer (G), and optional cosmetic ingredients described later if desired.
  • the cosmetic composition synergistically increases the smoothness at the time of rinsing by having both the silicone compound (F) (hereinafter sometimes referred to as the component (F)) and the gloss composition.
  • the shampoo and rinse containing both the component (F) and the gloss composition can synergistically enhance the texture of the object to be treated, such as the volume of the hair after washing.
  • the reason why the smoothness at the time of rinsing can be synergistically increased or the texture of the object to be processed can be synergistically increased by having both the component (F) and the gloss composition is not clear, but is estimated as follows.
  • the glossy crystals contained in the glossy composition are elongated crystals having a minor axis / major axis ratio of less than 0.45. For this reason, when wash
  • This network structure has a relatively high moisture content, and it is easy to incorporate the component (F) into the network structure.
  • the network structure incorporating the component (F) adheres to the object to be treated. Cheap. For this reason, it is considered that more (F) component adheres to the processing target, and when the processing target is rinsed, the slip between the processing target and the fingers is improved, and the smoothness at the time of rinsing can be improved.
  • the mesh-like structure incorporating the component (F) can support the hair three-dimensionally and enhance the volume feeling.
  • the component (F) may be any component that can be conventionally blended in cosmetics, such as dimethylpolysiloxane (including highly polymerized dimethylpolysiloxane and silicone rubber), methylphenylpolysiloxane, polyether-modified silicone, polyamino.
  • Modified silicone betaine modified silicone, alcohol modified silicone, fluorine modified silicone, epoxy modified silicone, mercapto modified silicone, carboxy modified silicone, fatty acid modified silicone, silicone graft polymer, cyclic silicone, alkyl modified silicone, trimethylsilyl group terminated dimethylpolysiloxane, Examples thereof include silanol group-terminated dimethylpolysiloxane.
  • component (F) dimethylpolysiloxane, polyether-modified silicone, and polyamino-modified silicone are preferable, and highly polymerized dimethylpolysiloxane is more preferable from the viewpoint of further enhancing the synergistic effect with the gloss composition.
  • component (F) components may be used individually by 1 type, and may be used in combination of 2 or more type.
  • Component (F) may be a component emulsified and emulsified with a surfactant.
  • the highly polymerized dimethylpolysiloxane is a dimethylpolysiloxane having a kinematic viscosity at 25 ° C. of 5 million mm 2 / s or more.
  • the kinematic viscosity of the highly polymerized dimethylpolysiloxane is preferably 8 million mm 2 / s or more.
  • the upper limit of the kinematic viscosity is not particularly limited, but is preferably 30 million mm 2 / s. That is, the kinematic viscosity of the highly polymerized dimethylpolysiloxane is preferably 8 million mm 2 / s or more and 30 million mm 2 / s or less.
  • the kinematic viscosity is a value measured by the following measuring method.
  • a toluene solution (sample solution) of dimethylpolysiloxane having a concentration of 1 g / 100 mL is prepared, and the specific viscosity ⁇ sp (25 ° C.) is obtained by the following formula (1).
  • the obtained specific viscosity ⁇ sp is substituted into the Huggins relational expression shown in the following formula (2) to determine the intrinsic viscosity [ ⁇ ].
  • the Huggins constant a value described in “Nakamuta,“ Journal of the Chemical Society of Japan ”, No. 77, page 588, 1956” is used.
  • the obtained [ ⁇ ] is represented by A.
  • the molecular weight M of dimethylpolysiloxane is determined.
  • the obtained M is represented by A. J. et al.
  • the kinematic viscosity ⁇ of dimethylpolysiloxane is determined.
  • ⁇ sp ( ⁇ / ⁇ 0) ⁇ 1 (1)
  • ⁇ 0 represents the viscosity of toluene
  • represents the viscosity of the sample solution.
  • ⁇ sp [ ⁇ ] + K ′ [ ⁇ ] 2 (2)
  • K ′ is a Huggins constant.
  • [ ⁇ ] 0.215 ⁇ 10 ⁇ 4 M 0.65 (3)
  • M is the molecular weight of dimethylpolysiloxane.
  • log ⁇ 1.00 + 0.0123M 0.5 (4)
  • M is the molecular weight of dimethylpolysiloxane.
  • Said (eta) 0 and (eta) are the viscosity measured based on cosmetics raw material reference
  • the highly polymerized dimethylpolysiloxane includes trimethylsilyl group-terminated dimethylpolysiloxane, silanol group-terminated dimethylpolysiloxane, and the like.
  • the highly polymerized dimethylpolysiloxane may be used singly or in combination of two or more.
  • the form of the highly polymerized dimethylpolysiloxane may be a molten liquid or an emulsion.
  • the emulsifier and emulsification method in emulsification are not particularly limited.
  • the content of the component (F) in the cosmetic is determined in consideration of the type of cosmetic.
  • the content of the component (F) in the shampoo is preferably 0.5 to 5% by mass and more preferably 1 to 4% by mass with respect to the total mass of the shampoo. If it is less than the above lower limit value, the smoothness during rinsing and the texture of the object to be treated may be reduced, and if it exceeds the above upper limit value, the stickiness of the hair after drying may be increased.
  • the mass ratio represented by component (A) / component (F) (hereinafter sometimes referred to as A / F ratio) is determined in consideration of the type of cosmetics and the like.
  • the A / F ratio is preferably 0.06 to 60, more preferably 0.2 to 40, and even more preferably 1 to 20. If it is less than the lower limit, the smoothness during rinsing with the component (F) may be reduced, and if it exceeds the upper limit, stickiness of the hair after drying may be increased.
  • the cosmetic can synergistically increase the smoothness during rinsing by having both the cationic polymer (G) (hereinafter sometimes referred to as the component (G)) and the gloss composition.
  • the shampoo and rinse containing both the component (G) and the gloss composition can synergistically enhance the texture of the treatment target such as the volume of hair after washing.
  • the reason why the smoothness at the time of rinsing can be increased synergistically or the texture of the object to be processed can be increased synergistically by having both the component (G) and the gloss composition is not clear, but is estimated as follows.
  • the network structure incorporating the component (G) adheres to the object to be treated. Cheap. For this reason, it is considered that more (G) components are attached to the processing target, and when the processing target is rinsed, the slip between the processing target and the fingers is improved, and the smoothness at the time of rinsing can be increased. In addition, it is considered that the mesh-like structure incorporating the component (G) can enhance the volume feeling by supporting the hair three-dimensionally.
  • the component (G) may be any component that can be blended in cosmetics, and examples thereof include cationized cellulose, cationized guar gum, dimethyldiallylammonium chloride / acrylamide copolymer, cationized dextran, and cationized pullulan. Can be mentioned. Of these, cationized guar gum and dimethyldiallylammonium chloride / acrylamide copolymer are preferred from the viewpoint of further enhancing the synergistic effect with the gloss composition.
  • the content of the component (G) in the cosmetic is determined in consideration of the type of cosmetic.
  • the content of the component (G) in the shampoo is preferably 0.01 to 5% by mass and more preferably 0.1 to 2% by mass with respect to the total mass of the shampoo. . If it is less than the above lower limit value, the smoothness at the time of rinsing and the texture of the object to be processed may be reduced, and if it exceeds the above upper limit value, it may be easily wet during the rinsing.
  • the mass ratio represented by component (A) / component (G) (hereinafter sometimes referred to as A / G ratio) is determined in consideration of the type of cosmetics and the like.
  • the A / G ratio is preferably 0.2 to 2000, more preferably 5 to 200. If it is less than the lower limit, the smoothness during rinsing may be reduced, and if it exceeds the upper limit, stickiness of the hair after drying may be increased.
  • the cosmetic may contain optional components other than the gloss composition and the components (F) to (G) (hereinafter sometimes referred to as cosmetic optional components) as necessary.
  • Cosmetic optional ingredients include surfactants; anionic polymers, nonionic polymers, etc., polymers other than (F) and (G) ingredients (arbitrary polymers); polyols; inorganic salts such as salt and salt cake; organic salts Humectants such as propylene glycol; tonic agents; solubilizers; antioxidants such as BHT and ⁇ -tocopherol; bactericides such as triclosan and trichlorocarban; viscosity modifiers such as fatty acid monoethanolamide and fatty acid diethanolamide; Absorbents; Antioxidants; Protein derivatives; Animal and plant extracts; Antidandruff agents such as piroctone olamine and zinc pyrithione; Anti-inflammatory agents such as dipotassium glycyrrhizinate; ; PH adjust
  • surfactant as a cosmetic optional component examples include the same components as the component (B).
  • Optional polymers for cosmetic ingredients include pectin, carrageenan, guar gum, locust bean gum, gelatin, xanthan gum, carboxyvinyl polymer, carboxymethylhydroxyethylcellulose, hydroxyethylcellulose, hydroxypropylmethylcellulose, alginate, starch, polyvinyl alcohol, polyacrylic Examples include acid salts, polymethacrylates, polymethyl acrylates, polyethylene glycols, polyethylene oxides, and tragarant rubbers.
  • the type of cosmetic optional ingredients to be blended is appropriately determined in consideration of functions required for cosmetics.
  • the content of the cosmetic optional ingredient in the cosmetic is appropriately determined in consideration of the type of cosmetic optional ingredient.
  • the method for producing the cosmetic is not particularly limited, and examples thereof include a method of dispersing the gloss composition, the components (F) to (G) and optional cosmetic ingredients in a dispersion medium such as water. .
  • the order of adding each component to the dispersion medium is not particularly limited.
  • “dispersion” means that each component does not settle in the dispersion medium.
  • the gloss composition of the present invention comprises gloss crystals containing the component (A) and the components (B) to (D), and the minor crystal / major axis ratio of the gloss crystals is less than 0.45, Since the C / A ratio is in a specific range, the cosmetic is given a good gloss, and the smoothness of the cosmetic during rinsing and the texture of the treatment target can be further enhanced.
  • the mass ratio represented by the component (C) / the component (A) is 0.2 to 1.5,
  • the ratio represented by the minor axis / major axis of the crystal is a gloss composition having a ratio of 0.10 or more and less than 0.45;
  • the component (A) is 2% by mass or more and 10% by mass or less
  • the component (B) is 5% by mass or more and 30% by mass or less
  • the component (C) is 1% by mass or more and 10% by mass or less
  • R 1 represents a hydrocarbon group having 13 to 21 carbon atoms
  • R 2 represents an alkylene group having 2 to 4 carbon atoms
  • m represents an average number of repetitions of (R 2 O)
  • Y represents a hydrogen atom or R 3 CO—
  • R 3 represents a hydrocarbon group having 13 to 21 carbon atoms.
  • the mass ratio represented by the component (C) / component (A) is 0.2 to 1.5;
  • the ratio represented by the minor axis / major axis of the crystal is a gloss composition having a ratio of 0.10 or more and less than 0.45;
  • the component (A) is 2% by mass or more and 10% by mass or less,
  • the component (B) is 5% by mass or more and 30% by mass or less,
  • the component (C) is 1% by mass or more and 10% by mass or less,
  • the component (D) is 25 to 90% by mass
  • Examples include a gloss composition in which the component (E) is 0.2 to 3% by mass and the total amount
  • the mass ratio represented by the component (C) / component (A) is 0.2 to 1.5;
  • the ratio represented by the minor axis / major axis of the crystal is a gloss composition having a ratio of 0.10 or more and less than 0.45; With respect to the total mass of the gloss composition,
  • the component (A) is 2% by mass or more and 10% by mass or less,
  • the component (B) is 5% by mass or more and 30% by mass or less
  • the component (C) is 1% by mass or more
  • a gloss composition a silicone compound (F), a cationic polymer (G), a dispersion medium, and optionally a cosmetic optional component;
  • the gloss composition is the gloss composition of the present invention described above,
  • the component (F) is at least one selected from the group consisting of dimethylpolysiloxane, polyether-modified silicone, and polyamino-modified silicone,
  • Component (G) is at least one selected from the group consisting of cationized guar gum and dimethyldiallylammonium chloride-acrylamide copolymer;
  • the component (A) is 2% by mass or more and 10% by mass or less,
  • the component (B) is 5% by mass or more and 30% by mass or less,
  • the component (C) is 1% by mass or more and 10% by mass or less;
  • the content of (F) is 0.5 to 5% by mass
  • the content of (G) is 0.01 to 5%
  • a gloss composition a silicone compound (F), a cationic polymer (G), a dispersion medium, and optionally a cosmetic optional component;
  • the gloss composition is the gloss composition of the present invention described above, (F) component is highly polymerized dimethylpolysiloxane,
  • the component (G) is at least one selected from the group consisting of cationized guar gum and dimethyldiallylammonium chloride / acrylamide copolymer,
  • the cosmetic optional ingredient includes at least one selected from the group consisting of a surfactant, a fragrance, and citric acid;
  • the component (A) is 2% by mass or more and 10% by mass or less,
  • the component (B) is 5% by mass or more and 30% by mass or less,
  • the component (C) is 1% by mass or more and 10% by mass or less;
  • the content of (F) is 0.5 to 5% by mass,
  • the content of (F) is 0.5 to 5% by mass,
  • B-1 Polyoxyethylene (average 3 mol) ammonium lauryl ether sulfate (Texapon ALES 70 (trade name), manufactured by Cognis Japan, pure content 70% by mass).
  • B-2 Ammonium lauryl sulfate (Texapon ALICS T (trade name), manufactured by Cognis Japan Co., Ltd.).
  • B-3 Polyoxyethylene (average 2 moles) sodium lauryl ether sulfate (Sinoline SPE-1250 (trade name), manufactured by Shin Nippon Rika Co., Ltd., pure content: 70% by mass).
  • C-1 Lauryl alcohol (Conol 20P (trade name), manufactured by Shin Nippon Chemical Co., Ltd., melting point 23 ° C.).
  • C-2 Cetyl alcohol (LANETTE 16 (trade name), manufactured by Cognis Japan, melting point 50 ° C.).
  • C-3 Stearyl alcohol (LANETTE 18 (trade name), manufactured by Cognis Japan, melting point 60 ° C.).
  • C-4 Behenyl alcohol (LANETTE 22 (trade name), manufactured by Cognis Japan, melting point 75 ° C.).
  • E-1 Sodium benzoate (sodium benzoate (trade name), manufactured by BFGoodrich Kalama Inc.).
  • F-1 Highly polymerized dimethyl silicone (silicone emulsion (6) (trade name), manufactured by Yushi Kogyo Co., Ltd., emulsion, pure content 60 mass%).
  • G-1 Cationized guar gum (Labor gum CG-M6L (trade name), manufactured by Dainippon Pharmaceutical Co., Ltd.).
  • G-2 Dimethyldiallylammonium chloride / acrylamide copolymer (Kayacrill Resin M-50 (trade name), manufactured by Nippon Kayaku Co., Ltd.).
  • Perfume B described in Tables 5 to 10 of JP-A-2006-63044.
  • Citric acid manufactured by Fuso Chemical Industries.
  • Examples 1-1 to 1-10 Comparative Examples 1-2 to 1-3
  • 600 g of the gloss composition of each example was prepared by the following procedure.
  • the gloss composition in each example was prepared under the condition of an environmental temperature of 25 ° C.
  • the compounding amount of each component in the table is a pure conversion amount (the same applies hereinafter).
  • three one motor FBL1200, (Made by HEIDON) for 20 minutes (first mixing operation).
  • (A) component was added to the primary mixture with (B) component, (C) component, (D) component, and (E) component, and it was set as the secondary mixture.
  • a micropump model number 184-405, manufactured by Chuo Rika Co., Ltd.
  • the secondary mixture was placed in a beaker and a line homomixer (ROBOMIX f-model, manufactured by Primix, stirring condition: 4500 rpm) at 25 g / min for 10 minutes.
  • the mixture was circulated to obtain a mixture (second mixing operation, mixing step). At this point, heating of the mixture was stopped.
  • the mixture in the beaker was circulated at a rate of 25 g / min between the beaker and a cooler (aluminum spiral heat exchanger).
  • the cooling temperature of the cooler was set as “Cooling temperature” in the table.
  • the mixture was circulated through the beaker and the cooler until the mixture in the beaker reached the “crystallization end temperature” in the table, and gloss compositions P1 to P10 and P′2 to P′3 were obtained (crystallization). Process).
  • the crystallization method of this example was described as “circulation”. About the obtained glossy composition, the minor axis / major axis ratio of the glossy crystals was measured.
  • Example 1-11 After the crystallization step, a glossy composition P11 was obtained in the same manner as in Example 1-1 except that the glossy composition was left in a constant temperature bath at 48 ° C. (aging step). The aging time is as shown in the table. About the obtained glossy composition, the minor axis / major axis ratio of the glossy crystals was measured.
  • Example 1-1 A glossy composition was obtained in the same manner as in Example 1-1 except that the crystallization process was as follows. The mixture in the beaker was passed through the cooler once with a micro pump to obtain a glossy composition P′1 (crystallization step). At this time, the flow rate of the mixture was adjusted so that the temperature of the mixture at the outlet of the cooler was 35 ° C. The aging process is under the same conditions as in Example 1-1. About the obtained glossy composition, the minor axis / major axis ratio of the glossy crystals was measured. In the table, the crystallization method of this example was described as “one pass”.
  • FIG. 2 is a photomicrograph of the glossy composition P1 obtained in Example 1-1 (magnification 40 times)
  • FIG. 3 is a photomicrograph of the glossy composition P11 obtained in Example 1-11 (magnification 40 times).
  • FIG. 4 is a photomicrograph (magnification 40 times) of the glossy composition P′1 obtained in Comparative Example 1-1.
  • the glossy crystals of the glossy composition P1 and the glossy composition P11 were needle-like with a minor axis / major axis ratio.
  • the glossy crystal of the glossy composition P′1 had a large minor axis / major axis ratio.
  • Examples 2-1 to 2-11, Comparative Examples 2-1 to 2-3 According to Tables 3 to 4, each component except the glossy composition and citric acid was placed in a 200 mL beaker and stirred at 25 ° C. for 30 minutes. The gloss composition was added and stirred for 10 minutes, and then adjusted to pH 6 with citric acid to obtain 100 g of each shampoo. About the obtained shampoo, the appearance, the smoothness at the time of rinsing, and the volume of hair were evaluated, and the results are shown in the table.
  • the gloss compositions used in each example are the gloss compositions P1 to P11 and P′1 to P′3 obtained in Examples 1-1 to 1-11 and Comparative Examples 1-1 to 1-3.
  • suitable amount which is the blending amount of citric acid indicates the amount required to bring the shampoo to pH 6, and is 0.8 to 1.3% by mass relative to the total mass of the shampoo.
  • balance which is the blending amount of purified water, indicates the amount required to make the shampoo 100% by mass.
  • each of Examples 2-1 to 2-11 to which the present invention was applied had a pearly luster, an evaluation of smoothness at the time of rinsing of 12 points or more, and the volume of hair.
  • the evaluation was 12 points or more.
  • Comparative Examples 2-1 to 2-3 using a glossy composition having a minor axis / major axis ratio of 0.45 or more of glossy crystals have a pearly luster, but have a smoothness of -10 points or less when rinsed.
  • the volume of hair was -12 points or less. From these results, it was found that by applying the present invention, a pearly luster was imparted to the cosmetic, and the smoothness at the time of rinsing in the cosmetic and the texture of the treatment object could be further enhanced.
  • a pearly luster is imparted to the cosmetic, and the smoothness of the cosmetic during rinsing and the texture of the treatment object can be further enhanced, which is extremely important in industry.

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Abstract

A gloss composition which contains: crystals containing a fatty acid glycol ester (A) represented by general formula (I) (wherein R1 represents a hydrocarbon group having 13-21 carbon atoms; R2 represents an alkylene group having 2-4 carbon atoms; m represents a number of 1-3, which is the average number of repetitions of (R2O); Y represents a hydrogen atom or R3CO-; and R3 represents a hydrocarbon group having 13-21 carbon atoms), a surfactant (B), an alcohol (C) having 8-22 carbon atoms, and water (D). In this gloss composition, the mass ratio of the component (C) to the component (A), namely, component (C)/component (A) is 0.2-1.5, and the breadth/length ratio of the crystals is less than 0.45. Y-O-(R2O)m-CO-R1 (I)

Description

光沢組成物及びその製造方法、ならびに化粧料Glossy composition, method for producing the same, and cosmetics
 本発明は、光沢組成物及びその製造方法、ならびに化粧料に関する。
 本願は、2013年10月21日に、日本に出願された特願2013-218275号に基づき優先権を主張し、その内容をここに援用する。
The present invention relates to a gloss composition, a method for producing the same, and a cosmetic.
This application claims priority on October 21, 2013 based on Japanese Patent Application No. 2013-218275 for which it applied to Japan, and uses the content here.
シャンプー、リンス、ボディーシャンプー等の化粧料には、例えばパール様の光沢を与えるために、光沢組成物が用いられている。光沢組成物としては、脂肪酸グリコールエステル、界面活性剤、水及び晶析添加剤を含有する光沢組成物が知られている(例えば、特許文献1)。 For cosmetics such as shampoos, rinses and body shampoos, a gloss composition is used to give a pearly luster, for example. As the gloss composition, a gloss composition containing a fatty acid glycol ester, a surfactant, water and a crystallization additive is known (for example, Patent Document 1).
従来、化粧料の付加価値をさらに高めるために、パール様の外観を持ちつつ、すすぎ時のなめらかさや、頭髪にボリューム感を与えたり、肌にうるおいを与えたりする等、処理対象の質感の向上を図った化粧料が提案されている。
例えば、アニオン界面活性剤と、特定の平均粒子径のシリコーン誘導体と、融点が55~75℃にあり、少なくとも一部が結晶形で存在し、その長径に対する短径の割合が0.75以下の結晶型を有するパール化剤と、特定のアルコールとを含有する液体洗浄剤組成物が提案されている(例えば、特許文献2)。
Conventionally, in order to further increase the added value of cosmetics, while maintaining a pearl-like appearance, improving the texture of the processing object, such as smoothness when rinsing, volume on the hair, moisture on the skin, etc. Cosmetics designed for the purpose have been proposed.
For example, an anionic surfactant, a silicone derivative having a specific average particle diameter, a melting point of 55 to 75 ° C., at least a part of the crystalline form exists, and the ratio of the short diameter to the long diameter is 0.75 or less. A liquid detergent composition containing a pearlizing agent having a crystal form and a specific alcohol has been proposed (for example, Patent Document 2).
特開2010-95518号公報JP 2010-95518 A 特開2000-290148号公報JP 2000-290148 A
 しかしながら、化粧料には、すすぎ時のなめらかさと処理対象の質感とのさらなる向上が求められている。
 そこで、本発明は、化粧料にパール様の光沢を付与し、かつ化粧料におけるすすぎ時のなめらかさと処理対象の質感とをより高められる光沢組成物の提供を目的とする。
However, cosmetics are required to further improve smoothness during rinsing and texture to be processed.
Therefore, an object of the present invention is to provide a glossy composition that imparts a pearly luster to a cosmetic and can further enhance the smoothness of the cosmetic during rinsing and the texture to be treated.
本発明者らは、鋭意検討した結果、短径/長径で表される比が0.45未満の結晶を含有する光沢組成物を用いることで、化粧料におけるすすぎ時のなめらかさと処理対象の質感とをより高められることを見出し、本発明に至った。 As a result of intensive studies, the present inventors have used a glossy composition containing crystals having a minor axis / major axis ratio of less than 0.45, so that smoothness during rinsing in cosmetics and the texture of the object to be treated are obtained. As a result, the present invention has been found.
本発明は、以下の[1]~[4]の態様を有する。
[1]下記一般式(I)で表される脂肪酸グリコールエステル(A)を含有する結晶と、界面活性剤(B)と、炭素数8~22のアルコール(C)と、水(D)とを併有し、前記(C)成分/前記(A)成分で表される質量比が0.2~1.5であり、前記結晶の短径/長径で表される比は、0.45未満である光沢組成物。
 Y-O-(RO)-CO-R ・・・(I)
 ((I)式中、Rは、炭素数13~21の炭化水素基を表し、Rは、炭素数2~4のアルキレン基を表し、mは、(RO)の平均繰り返し数を表す1~3の数である。Yは、水素原子又はRCO-を表し、Rは、炭素数13~21の炭化水素基を表す。) 
[2]芳香族カルボン酸又はその塩(E)を併有する[1]に記載の光沢組成物。
[3][1]又は[2]に記載の光沢組成物を含有する化粧料。
[4][1]に記載の光沢組成物の製造方法であって、前記(A)~(D)成分を前記(A)成分の融点以上で混合して混合物を得る混合工程と、晶析槽と冷却器とが接続された製造装置を用い、前記混合物を前記晶析槽と前記冷却器とに循環させて、前記(A)成分の凝固点以下の温度に冷却する晶析工程と、を有する光沢組成物の製造方法。
The present invention has the following aspects [1] to [4].
[1] A crystal containing a fatty acid glycol ester (A) represented by the following general formula (I), a surfactant (B), an alcohol (C) having 8 to 22 carbon atoms, water (D), The mass ratio represented by the component (C) / the component (A) is 0.2 to 1.5, and the ratio represented by the minor axis / major axis of the crystal is 0.45. A gloss composition that is less than.
Y—O— (R 2 O) m —CO—R 1 (I)
(In the formula (I), R 1 represents a hydrocarbon group having 13 to 21 carbon atoms, R 2 represents an alkylene group having 2 to 4 carbon atoms, and m represents an average number of repetitions of (R 2 O). Y represents a hydrogen atom or R 3 CO—, and R 3 represents a hydrocarbon group having 13 to 21 carbon atoms.)
[2] The gloss composition according to [1], which also contains an aromatic carboxylic acid or a salt thereof (E).
[3] A cosmetic comprising the gloss composition according to [1] or [2].
[4] The method for producing a glossy composition according to [1], wherein the components (A) to (D) are mixed at a melting point or higher of the component (A) to obtain a mixture; A crystallization step of circulating the mixture to the crystallization tank and the cooler and cooling the mixture to a temperature below the freezing point of the component (A) using a production apparatus in which a tank and a cooler are connected. A method for producing a gloss composition.
 即ち、本発明は以下に関する。
[1’]下記一般式(I)で表される脂肪酸グリコールエステル(A)と、界面活性剤(B)と、炭素数8~22のアルコール(C)と、水(D)とを含み;
  前記(C)成分/前記(A)成分で表される質量比が0.2~1.5であり; 
 前記結晶の短径/長径で表される比は、0.45未満である
 前記光沢組成物:
 Y-O-(RO)-CO-R ・・・(I)
 ((I)式中、Rは、炭素数13~21の炭化水素基を表し;Rは、炭素数2~4のアルキレン基を表し;mは、(RO)の平均繰り返し数を表す1~3の数であり;Yは、水素原子又はRCO-を表し;Rは、炭素数13~21の炭化水素基を表す。)
[2’]さらに、芳香族カルボン酸又はその塩(E)を含む[1’]に記載の光沢組成物。
[3’][1’]又は[2’]に記載の光沢組成物を含有する化粧料。
[4’] 晶析槽と冷却機とを備えた製造装置を用いる[1’]に記載の光沢組成物の製造方法であって、
 前記製造装置は、前記晶析槽と前記冷却機とが接続されており、
 前記製造方法は、
前記(A)~(D)成分を前記(A)成分の融点以上で混合して混合物を得る混合工程と、
 前記混合物を前記晶析槽と前記冷却機とに循環させて、前記(A)成分の凝固点以下の温度に冷却し、前記(A)成分含有する結晶を析出させる晶析工程と、
 を含む光沢組成物の製造方法。
That is, the present invention relates to the following.
[1 ′] a fatty acid glycol ester (A) represented by the following general formula (I), a surfactant (B), an alcohol (C) having 8 to 22 carbon atoms, and water (D);
The mass ratio represented by the component (C) / component (A) is 0.2 to 1.5;
The ratio represented by the minor axis / major axis of the crystal is less than 0.45. The gloss composition:
Y—O— (R 2 O) m —CO—R 1 (I)
(In the formula (I), R 1 represents a hydrocarbon group having 13 to 21 carbon atoms; R 2 represents an alkylene group having 2 to 4 carbon atoms; m represents an average number of repetitions of (R 2 O)) Y represents a hydrogen atom or R 3 CO—; R 3 represents a hydrocarbon group having 13 to 21 carbon atoms.)
[2 ′] The gloss composition according to [1 ′], further comprising an aromatic carboxylic acid or a salt thereof (E).
[3 ′] A cosmetic containing the gloss composition according to [1 ′] or [2 ′].
[4 ′] The method for producing a glossy composition according to [1 ′] using a production apparatus including a crystallization tank and a cooler,
In the manufacturing apparatus, the crystallization tank and the cooler are connected,
The manufacturing method includes:
A mixing step of mixing the components (A) to (D) above the melting point of the component (A) to obtain a mixture;
A crystallization step of circulating the mixture through the crystallization tank and the cooler, cooling the mixture to a temperature below the freezing point of the component (A), and precipitating the crystals containing the component (A);
A method for producing a glossy composition comprising:
 本発明の光沢組成物によれば、化粧料にパール様の光沢を付与し、かつ化粧料におけるすすぎ時のなめらかさと処理対象の質感とをより高められる。 According to the gloss composition of the present invention, a pearl-like gloss is imparted to the cosmetic, and the smoothness of the cosmetic during rinsing and the texture of the treatment target can be further enhanced.
本発明の一実施形態である光沢組成物の製造に用いられる光沢組成物の製造装置の一例を示す模式図である。It is a schematic diagram which shows an example of the manufacturing apparatus of the glossy composition used for manufacture of the glossy composition which is one Embodiment of this invention. 実施例1-1の光沢組成物の顕微鏡写真である。2 is a photomicrograph of the gloss composition of Example 1-1. 実施例1-11の光沢組成物の顕微鏡写真である。2 is a photomicrograph of the gloss composition of Example 1-11. 比較例1-1の光沢組成物の顕微鏡写真である。2 is a photomicrograph of the gloss composition of Comparative Example 1-1.
 (光沢組成物)
 本発明の一実施形態である光沢組成物は、下記一般式(I)で表される脂肪酸グリコールエステル(A)を含有する結晶(以下、光沢結晶という)と、界面活性剤(B)と、炭素数8~22のアルコール(C)と、水(D)とを含む組成物であり、例えば、前記光沢結晶が水中に分散している組成物である。本発明における「光沢組成物」とは、化粧料等にパール様の光沢を与える組成物を意味する。化粧料としては、ヘアシャンプー、ボディーシャンプー、ハンドソープ、フェイスソープ等の身体用の液体洗浄剤;ヘアリンス、ボディートリートメント等の身体用のケア製剤等、頭髪や肌を洗浄したり、洗浄後の頭髪や肌の手入れに用いられる液体製剤が挙げられる。
 なお、ここでいう「分散」とは水中に光沢結晶が沈降していない状態であることを意味する。
 「結晶」とは、非晶質の固体を含んでいてもよい。
(Glossy composition)
The gloss composition according to an embodiment of the present invention includes a crystal (hereinafter referred to as gloss crystal) containing a fatty acid glycol ester (A) represented by the following general formula (I), a surfactant (B), A composition containing alcohol (C) having 8 to 22 carbon atoms and water (D), for example, a composition in which the glossy crystals are dispersed in water. The “gloss composition” in the present invention means a composition that imparts pearly luster to cosmetics and the like. Cosmetics include body shampoos, body shampoos, hand soaps, face soaps, and other body care products; hair rinses, body treatments and other body care products, and hair and skin after washing. And liquid preparations used for skin care.
Here, “dispersion” means that the glossy crystals are not settled in water.
“Crystal” may include an amorphous solid.
 Y-O-(RO)-CO-R ・・・(I)
 ((I)式中、Rは、炭素数13~21の炭化水素基を表し;Rは、炭素数2~4のアルキレン基を表し;mは、(RO)の平均繰り返し数を表す1~3の数であり;Yは、水素原子又はRCO-を表し;Rは、炭素数13~21の炭化水素基を表す。)
Y—O— (R 2 O) m —CO—R 1 (I)
(In the formula (I), R 1 represents a hydrocarbon group having 13 to 21 carbon atoms; R 2 represents an alkylene group having 2 to 4 carbon atoms; m represents an average number of repetitions of (R 2 O)) Y represents a hydrogen atom or R 3 CO—; R 3 represents a hydrocarbon group having 13 to 21 carbon atoms.)
 光沢結晶は、短径/長径で表される比(以下、短径/長径比ということがある)が0.45未満であり、短径/長径比が0.35未満が好ましく、短径/長径比が0.30未満がより好ましい。
短径/長径比が上記上限値未満であれば、化粧料におけるすすぎ時のなめらかさと処理対象の質感とを高められる。これは、光沢結晶同士が絡み合って、化粧料中の他の成分(例えば、後述するシリコーン化合物やカチオン性ポリマー等)を取り込み、処理対象である頭髪や肌等に付着しやすくなるためと考えられる。
なお、「光沢結晶同士が絡み合う」とは、長径方向の側面で重なり合うのでなく、末端部分同志または末端部分と側面部分で触れあっている状態を意味する。
 光沢結晶の短径/長径比の下限は、特に限定されないが、実質的に0.10であり、製造効率の観点からは0.20が好ましい。
即ち、光沢結晶は、短径/長径で表される比が、0.10以上、0.45未満が好ましく、0.10以上、0.35未満がより好ましく、0.20以上、0.35未満がさらに好ましく、0.20以上、0.30未満が特に好ましい。
光沢結晶の短径/長径比は、顕微鏡を用いて任意の10個の光沢結晶の長径及び短径をそれぞれ測定し、測定された長径の平均値と短径の平均値とをそれぞれ算出し、これら算出された値から短径/長径をさらに算出して得られた値(即ち、短径/長径比の平均値)である。
 なお、ここでいう光沢結晶の「長径」とは、光沢結晶の大きさにおける最大値を意味し、「短径」とは、光沢結晶の大きさにおける最小値を意味する。
 光沢組成物に含まれる光沢結晶のうち、短径/長径比が0.45未満の光沢結晶の割合(以下、長結晶率ということがある)は、光沢組成物に含まれる光沢結晶の総個数に対して、50%(個数換算)以上が好ましく、75%以上がより好ましく、100%であってもよい。長結晶率が上記下限値以上であれば、化粧料におけるすすぎ感のなめらかさや処理対象の質感のさらなる向上を図れる。
長結晶率は、得られた分散液をイオン交換水で20倍希釈して顕微鏡で5視野以上撮影し、それぞれの視野から任意に50個の結晶の短径と長径を計測することにより求めることができる。
The glossy crystal has a minor axis / major axis ratio (hereinafter sometimes referred to as minor axis / major axis ratio) of less than 0.45, preferably a minor axis / major axis ratio of less than 0.35, The major axis ratio is more preferably less than 0.30.
If the ratio of the minor axis / major axis is less than the above upper limit, the smoothness at the time of rinsing in the cosmetic and the texture of the treatment object can be enhanced. This is thought to be because gloss crystals are entangled with each other and other components in the cosmetic (for example, silicone compounds and cationic polymers described later) are taken in and easily attached to the hair or skin to be treated. .
Note that “the glossy crystals are intertwined” means a state in which the end portions are in contact with each other or the end portions and the side portions do not overlap on the side surfaces in the major axis direction.
The lower limit of the minor axis / major axis ratio of the glossy crystal is not particularly limited, but is substantially 0.10, and is preferably 0.20 from the viewpoint of production efficiency.
That is, in the glossy crystal, the ratio expressed by the minor axis / major axis is preferably 0.10 or more and less than 0.45, more preferably 0.10 or more and less than 0.35, and more preferably 0.20 or more and 0.35. Is more preferably 0.20 or more and less than 0.30.
The minor axis / major axis ratio of the glossy crystals is determined by measuring the major axis and minor axis of any 10 glossy crystals using a microscope, and calculating the average value of the measured major axis and the average value of the minor axis, It is a value obtained by further calculating the minor axis / major axis from these calculated values (that is, the average value of the minor axis / major axis ratio).
Here, the “major axis” of the glossy crystal means the maximum value in the size of the glossy crystal, and the “minor axis” means the minimum value in the size of the glossy crystal.
The percentage of glossy crystals having a minor axis / major axis ratio of less than 0.45 among the glossy crystals contained in the glossy composition (hereinafter sometimes referred to as long crystal ratio) is the total number of glossy crystals contained in the glossy composition. On the other hand, it is preferably 50% (number conversion) or more, more preferably 75% or more, and may be 100%. If the long crystal ratio is equal to or higher than the lower limit, the smoothness of the rinsing feeling in the cosmetic and the texture of the treatment target can be further improved.
The long crystal ratio is obtained by diluting the obtained dispersion 20 times with ion-exchanged water, photographing with 5 or more fields of view with a microscope, and arbitrarily measuring the short and long diameters of 50 crystals from each field. Can do.
光沢結晶の大きさは、特に限定されないが、例えば、長径は0.8μm以上が好ましく、1.5μm以上がより好ましく、2.0μm以上がさらに好ましい。上記下限値未満では、光沢結晶同士が絡み合いにくくなり、化粧料におけるすすぎ時のなめらかさと処理対象の質感が低下するおそれがある。長径の上限値は、特に限定されず、例えば、4.0μmが好ましく、3.0μmがより好ましい。上記上限値超では、光沢結晶同士が絡み合ったものの大きさが大きくなりすぎて、べた付きを生じやすくなる。
即ち、光沢結晶の長径は、0.8μm以上、4.0μm以下が好ましく、1.5μm以上、4.0μm以下がより好ましく、2.0μm以上、4.0μm以下がさらに好ましく、2.0μm以上、3.0μm以下が特に好ましい。
光沢結晶の短径は、特に限定されず、0.3μm以上が好ましく、0.4μm以上がより好ましい。上記下限値未満では、すすぎ時に破砕されやすくなる。短径の上限値は、特に限定されず、例えば、1.2μm以下が好ましく、1.0μm以下がより好ましい。上記上限値超では、光沢結晶同士が絡み合いにくくなるためである。
即ち、光沢結晶の短径は、0.3μm以上、1.2μm以下が好ましく、0.4μm以上、1.2μm以下がより好ましく、0.3μm以上、1.0μm以下がさらに好ましく、0.4μm以上、1.0μm以下が特に好ましい。
The size of the glossy crystal is not particularly limited. For example, the major axis is preferably 0.8 μm or more, more preferably 1.5 μm or more, and further preferably 2.0 μm or more. If it is less than the said lower limit, it will become difficult to intertwine glossy crystals, and there exists a possibility that the smoothness at the time of a rinse in cosmetics and the texture of a process target may fall. The upper limit value of the major axis is not particularly limited, and is preferably 4.0 μm, for example, and more preferably 3.0 μm. Above the upper limit, the size of the tangled glossy crystals becomes too large and stickiness tends to occur.
That is, the major axis of the glossy crystal is preferably 0.8 μm or more and 4.0 μm or less, more preferably 1.5 μm or more and 4.0 μm or less, further preferably 2.0 μm or more and 4.0 μm or less, and 2.0 μm or more. 3.0 μm or less is particularly preferable.
The minor axis of the glossy crystal is not particularly limited, but is preferably 0.3 μm or more, and more preferably 0.4 μm or more. If it is less than the said lower limit, it will become easy to crush at the time of a rinse. The upper limit of the minor axis is not particularly limited, and is preferably 1.2 μm or less, and more preferably 1.0 μm or less. This is because when the value exceeds the upper limit, the glossy crystals are less likely to be entangled with each other.
That is, the minor axis of the glossy crystal is preferably 0.3 μm or more and 1.2 μm or less, more preferably 0.4 μm or more and 1.2 μm or less, further preferably 0.3 μm or more and 1.0 μm or less, and 0.4 μm. As mentioned above, 1.0 micrometer or less is especially preferable.
光沢組成物の粘度は、特に限定されず、例えば、50~200mPa・sが好ましい。
光沢組成物の粘度は、BL型粘度計(ローター:No.3、回転数:60rpm、測定温度:25℃、東機産業株式会社製)を用い、ローター回転開始60秒後に読み取られた値である。
本明細書において、粘度は、特に断りのない限り、25℃における値で定義する。すなわち、本明細書に規定した範囲外の値であっても、25℃における値に補正したとき本明細書に規定した範囲の粘度の値であれば、それらは本発明の範囲に含まれる。
The viscosity of the gloss composition is not particularly limited, and is preferably 50 to 200 mPa · s, for example.
The viscosity of the gloss composition is a value read 60 seconds after the start of rotor rotation using a BL type viscometer (rotor: No. 3, rotation speed: 60 rpm, measurement temperature: 25 ° C., manufactured by Toki Sangyo Co., Ltd.). is there.
In this specification, the viscosity is defined as a value at 25 ° C. unless otherwise specified. That is, even if the value is outside the range specified in the present specification, it is included in the scope of the present invention as long as it is a viscosity value within the range specified in the present specification when corrected to a value at 25 ° C.
<脂肪酸グリコールエステル(A)>
脂肪酸グリコールエステル(A)(以下、(A)成分ということがある)は、下記一般式(I)で表される。
 Y-O-(RO)-CO-R ・・・(I)
<Fatty acid glycol ester (A)>
The fatty acid glycol ester (A) (hereinafter sometimes referred to as the component (A)) is represented by the following general formula (I).
Y—O— (R 2 O) m —CO—R 1 (I)
(I)式中、Rは、炭素数13~21の炭化水素基を表す。
は、不飽和結合を有していてもよいし、不飽和結合を有していなくてもよい。Rとしては、アルキル基、及びアルケニル基が好ましい。
は、直鎖でもよいし、分岐鎖でもよい。
の炭素数は、13~21であり、16~20が好ましい。炭素数が上記下限値未満では、融点が低いため不安定になり、上記上限値超では、融点や凝固温度が高くなって、生産効率が低下する。
としては、例えば、ペンタデシル基、ヘプタデシル基、ヘンイコシル基等が好ましい。
Yは、水素原子又はRCO-を表す。Yが水素原子であれば、(A)成分はモノ脂肪酸エステルであり、YがRCO-であれば、(A)成分はジ脂肪酸エステルである。
Yが、RCO-である場合、Rとしては、Rと同様の基が挙げられる。Rは、Rと同じ基であってもよいし、異なる基であってもよい。
は、炭素数2~4のアルキレン基を表す。即ち、(RO)は炭素数2~4のオキシアルキレン基である。Rの炭素数は、2~3が好ましい。Rの炭素数が上記範囲内であれば、結晶化しやすい。
mは、(RO)の平均繰り返し数を表し、1~3の数であり、1~2がより好ましい。なお、mは整数であってもよく、小数を含んでもよい。
ここで「(RO)の平均繰り返し数」とは、使用する脂肪酸エステル1モルに対して付加させるROのモル数の平均を意味する。
mが上記範囲内であれば、非水溶性となり、界面活性剤(B)の存在下でも、安定した光沢結晶を得られる。
In the formula (I), R 1 represents a hydrocarbon group having 13 to 21 carbon atoms.
R 1 may have an unsaturated bond or may not have an unsaturated bond. R 1 is preferably an alkyl group or an alkenyl group.
R 1 may be a straight chain or a branched chain.
R 1 has 13 to 21 carbon atoms, preferably 16 to 20 carbon atoms. If the number of carbon atoms is less than the lower limit, the melting point is low and unstable, and if it exceeds the upper limit, the melting point and the solidification temperature increase, resulting in a decrease in production efficiency.
R 1 is preferably, for example, a pentadecyl group, a heptadecyl group, a heneicosyl group, or the like.
Y represents a hydrogen atom or R 3 CO—. When Y is a hydrogen atom, the component (A) is a mono fatty acid ester, and when Y is R 3 CO—, the component (A) is a di fatty acid ester.
Y is, when an R 3 CO-, as the R 3, include the same groups as R 1. R 3 may be the same group as R 1 or a different group.
R 2 represents an alkylene group having 2 to 4 carbon atoms. That is, (R 2 O) is an oxyalkylene group having 2 to 4 carbon atoms. R 2 preferably has 2 to 3 carbon atoms. If the carbon number of R 2 is within the above range, crystallization is easy.
m represents the average number of repetitions of (R 2 O) and is a number of 1 to 3, more preferably 1 to 2. Note that m may be an integer or may include a decimal.
Here, “the average number of repetitions of (R 2 O)” means the average number of moles of R 2 O added to 1 mole of the fatty acid ester used.
If m is in the above range, it becomes water-insoluble and stable glossy crystals can be obtained even in the presence of the surfactant (B).
(A)成分の融点は、50℃以上が好ましく、50~90℃がより好ましく、60~80℃がさらに好ましい。上記下限値未満では、界面活性剤(B)の存在下での光沢結晶の安定性が低下するおそれがあり、上記上限超では、融点が高いため、後述する混合工程において、界面活性剤(B)の安定性が低下するおそれがある。
(A)成分の凝固点は、80℃未満が好ましく、40~70℃がより好ましい。
The melting point of the component (A) is preferably 50 ° C. or higher, more preferably 50 to 90 ° C., and further preferably 60 to 80 ° C. If the amount is less than the lower limit, the stability of the glossy crystals in the presence of the surfactant (B) may be lowered. If the amount exceeds the upper limit, the melting point is high, so that the surfactant (B ) May decrease in stability.
The freezing point of component (A) is preferably less than 80 ° C, more preferably 40 to 70 ° C.
(A)成分としては、モノパルミチン酸エチレングリコール、モノステアリン酸エチレングリコール、モノイソステアリン酸エチレングリコール等のモノ脂肪酸エステルのモノエチレングリコール体;ジパルミチン酸エチレングリコール、ジステアリン酸エチレングリコール、ジベヘン酸エチレングリコール等のジ脂肪酸エステルのモノエチレングリコール体;モノ脂肪酸エステル又はジ脂肪酸エステルのジエチレングリコール体;モノ脂肪酸エステル又はジ脂肪酸エステルのトリエチレングリコール体等が挙げられる。中でも、(A)成分としては、モノエチレングリコール体が好ましく、ジ脂肪酸エステルのモノエチレングリコール体がより好ましく、ジステアリン酸エチレングリコールがさらに好ましい。
これらの(A)成分は、1種単独で用いられてもよいし、2種以上が組み合わされて用いられてもよい。
As component (A), monoethylene glycol form of mono fatty acid ester such as ethylene glycol monopalmitate, ethylene glycol monostearate, ethylene glycol monoisostearate; ethylene glycol dipalmitate, ethylene glycol distearate, ethylene glycol dibehenate Mono-fatty acid ester monoethylene glycol bodies; mono-fatty acid esters or di-fatty acid ester diethylene glycol bodies; mono-fatty acid esters or di-fatty acid ester triethylene glycol bodies, and the like. Among these, as the component (A), a monoethylene glycol body is preferable, a monoethylene glycol body of a difatty acid ester is more preferable, and ethylene glycol distearate is further preferable.
These (A) components may be used individually by 1 type, and may be used in combination of 2 or more type.
光沢組成物中の(A)成分の含有量の下限値は、光沢組成物の総質量に対して、2質量%が好ましく、3質量%がより好ましく、4質量%がさらに好ましい。光沢組成物中の(A)成分の含有量の上限値は、光沢組成物の総質量に対して、10質量%が好ましく、7質量%がより好ましく、6質量%がさらに好ましい。
即ち、光沢組成物中の(A)成分の含有量は、光沢組成物の総質量に対して、2質量%以上、10質量%以下が好ましく、3質量%以上、7質量%以下がより好ましく、4質量%以上、6質量%以下がさらに好ましい。
なお、ここでいう「(A)成分の含有量」とは、光沢組成物中における、結晶状態である(A)成分と結晶状態でない(A)成分の合計量を意味する。
上記下限値未満では、化粧料に十分な光沢を付与するために、光沢組成物の配合量を過度に高めなくてはならないおそれがある。上記上限値超では、流動性が損なわれて取り扱いが煩雑になるおそれがある。
The lower limit of the content of the component (A) in the gloss composition is preferably 2% by mass, more preferably 3% by mass, and still more preferably 4% by mass with respect to the total mass of the gloss composition. The upper limit of the content of the component (A) in the gloss composition is preferably 10% by mass, more preferably 7% by mass, and still more preferably 6% by mass with respect to the total mass of the gloss composition.
That is, the content of the component (A) in the gloss composition is preferably 2% by mass or more and 10% by mass or less, more preferably 3% by mass or more and 7% by mass or less with respect to the total mass of the gloss composition. 4 mass% or more and 6 mass% or less are more preferable.
In addition, "content of (A) component" here means the total amount of (A) component which is a crystalline state, and (A) component which is not a crystalline state in a glossy composition.
If it is less than the said lower limit, in order to provide sufficient gloss to cosmetics, there exists a possibility that the compounding quantity of a glossy composition must be raised too much. If it exceeds the upper limit, the fluidity may be impaired and handling may be complicated.
<界面活性剤(B)>
光沢組成物は、界面活性剤(B)(以下、(B)成分ということがある)を含有する。
(B)成分は、後述する光沢組成物の製造方法において、分散媒への(A)成分の分散性を高め、かつ光沢結晶の短径/長径比を小さくできる。
(B)成分としては、陰イオン性界面活性剤、非イオン性界面活性剤、及び両性界面活性剤等が挙げられる。
陰イオン性界面活性剤としては、例えば、炭素数8~22の高級脂肪酸塩、ポリオキシエチレンアルキルエーテルサルフェート、α-オレフィンスルホネート、アルキルスルホネート、アルキルサルフェート、N-アシルグルタミン酸塩等が挙げられる。また、陰イオン性界面活性剤の対イオンとしては、アルカリ金属イオン、アルカリ土類金属イオン、アンモニウムイオン、炭素数2又は3のアルカノール基を1~3個有するアルカノールアミン等が挙げられる。
非イオン性界面活性剤としては、ラウリン酸モノエタノールアミド、ヤシ油脂肪酸ジエタノールアミド、ポリオキシエチレンアルキルフェニルエーテル、ポリオキシエチレンアルキルエーテル、及びポリオキシエチレンラウリン酸モノエタノールアミド等が挙げられる。
両性界面活性剤としては、例えば、アルキルジメチルカルボキシメチルアンモニウムベタイン、アルキルカルボキシメチルイミダゾリウムベタイン、N-(N’-アシルアミノアルキル)-N-ヒドロキシアルキルアミノカルボン酸塩等が挙げられる。
(B)成分としては、(D)成分への(A)成分の分散性を高める観点から、陰イオン性界面活性剤が好ましく、ポリオキシエチレンアルキルエーエルサルフェートがより好ましく、エチレンオキシドを1~5モル付加した炭素数12~14のアルキル基を有する、ポリオキシエチレンアルキルエーテルサルフェートのアンモニウム塩又はナトリウム塩がより好ましい。
これらの(B)成分は、1種単独で用いられてもよいし、2種以上が組み合わされて用いられてもよい。
<Surfactant (B)>
The gloss composition contains a surfactant (B) (hereinafter sometimes referred to as component (B)).
The component (B) can increase the dispersibility of the component (A) in the dispersion medium and reduce the minor axis / major axis ratio of the glossy crystal in the method for producing a gloss composition described later.
Examples of the component (B) include anionic surfactants, nonionic surfactants, and amphoteric surfactants.
Examples of the anionic surfactant include higher fatty acid salts having 8 to 22 carbon atoms, polyoxyethylene alkyl ether sulfate, α-olefin sulfonate, alkyl sulfonate, alkyl sulfate, N-acyl glutamate and the like. Examples of the counter ion of the anionic surfactant include alkali metal ions, alkaline earth metal ions, ammonium ions, alkanolamines having 1 to 3 alkanol groups having 2 or 3 carbon atoms, and the like.
Examples of the nonionic surfactant include lauric acid monoethanolamide, coconut oil fatty acid diethanolamide, polyoxyethylene alkylphenyl ether, polyoxyethylene alkyl ether, and polyoxyethylene lauric acid monoethanolamide.
Examples of the amphoteric surfactant include alkyl dimethyl carboxymethyl ammonium betaine, alkyl carboxymethyl imidazolium betaine, N- (N′-acylaminoalkyl) -N-hydroxyalkylaminocarboxylate and the like.
As the component (B), an anionic surfactant is preferable from the viewpoint of enhancing the dispersibility of the component (A) in the component (D), polyoxyethylene alkyl ether sulfate is more preferable, and 1 to 5 mol of ethylene oxide is used. The ammonium salt or sodium salt of polyoxyethylene alkyl ether sulfate having an added alkyl group having 12 to 14 carbon atoms is more preferable.
These (B) components may be used individually by 1 type, and may be used in combination of 2 or more type.
光沢組成物中の(B)成分の含有量の下限値は、光沢組成物の総質量に対して、5質量%が好ましく、10質量%がより好ましい。光沢組成物中の(B)成分の含有量の上限値は、光沢組成物の総質量に対して、30質量%が好ましく、20質量%がより好ましい。即ち、光沢組成物中の(B)成分の含有量は、光沢組成物の総質量に対して、5質量%以上、30質量%以下が好ましく、10質量%以上、20質量%以下がより好ましい。上記下限値未満では、光沢結晶の短径/長径比を小さくしにくく、上記上限値超では、流動性が損なわれて取り扱いが煩雑になるおそれがある。 The lower limit of the content of the component (B) in the gloss composition is preferably 5% by mass and more preferably 10% by mass with respect to the total mass of the gloss composition. The upper limit of the content of the component (B) in the gloss composition is preferably 30% by mass and more preferably 20% by mass with respect to the total mass of the gloss composition. That is, the content of the component (B) in the gloss composition is preferably 5% by mass or more and 30% by mass or less, and more preferably 10% by mass or more and 20% by mass or less with respect to the total mass of the gloss composition. . If the ratio is less than the lower limit, it is difficult to reduce the minor axis / major axis ratio of the glossy crystal. If the ratio exceeds the upper limit, the fluidity is impaired and handling may be complicated.
光沢組成物中、(A)成分/(B)成分で表される質量比(以下、A/B比ということがある)は、0.1~0.5が好ましく、0.2~0.4がより好ましい。上記下限値以上であれば、後述する晶析工程において、光沢結晶を容易に析出でき、上記上限値以下であれば、微細な光沢結晶を得られやすい。 In the glossy composition, the mass ratio represented by component (A) / component (B) (hereinafter sometimes referred to as A / B ratio) is preferably 0.1 to 0.5, preferably 0.2 to 0.00. 4 is more preferable. If it is more than the said lower limit, a glossy crystal can be easily precipitated in the crystallization process mentioned later, and if it is below the said upper limit, it will be easy to obtain a fine glossy crystal.
<炭素数8~22のアルコール(C)>
光沢組成物は、炭素数8~22のアルコール(C)(以下、(C)成分ということがある)を含有する。(C)成分を含有することで、後述する光沢組成物の製造方法において、(D)成分への(A)成分の分散性を高め、微細で、短径/長径比のより小さい光沢結晶を得られる。
<Alcohol having 8 to 22 carbon atoms (C)>
The gloss composition contains an alcohol (C) having 8 to 22 carbon atoms (hereinafter sometimes referred to as component (C)). By containing the component (C), in the method for producing a gloss composition described later, the dispersibility of the component (A) in the component (D) is increased, and fine gloss crystals having a smaller minor axis / major axis ratio are obtained. can get.
(C)成分は、飽和の脂肪族アルコールでもよく不飽和の脂肪族アルコールでもよい。
(C)成分中の炭化水素基は、直鎖であってもよいし、分岐鎖であってもよい。より微細な光沢結晶を得る観点から、(C)成分としては、ラウリルアルコール、ミリスチルアルコール、セチルアルコール、ステアリルアルコール、ベヘニルアルコール等の炭素数12~22の脂肪族アルコールが好ましく、ラウリルアルコール、ミリスチルアルコール、セチルアルコール、ステアリルアルコール等の炭素数12~18の脂肪族アルコールがより好ましい。
The component (C) may be a saturated aliphatic alcohol or an unsaturated aliphatic alcohol.
The hydrocarbon group in component (C) may be linear or branched. From the viewpoint of obtaining finer glossy crystals, the component (C) is preferably an aliphatic alcohol having 12 to 22 carbon atoms such as lauryl alcohol, myristyl alcohol, cetyl alcohol, stearyl alcohol, behenyl alcohol, lauryl alcohol, myristyl alcohol, Aliphatic alcohols having 12 to 18 carbon atoms such as cetyl alcohol and stearyl alcohol are more preferred.
(C)成分としては、光沢結晶の短径/長径比をより小さくする観点から、セチルアルコール、ステアリルアルコールが好ましい。
これらの(C)成分は、1種単独で用いられてもよいし、2種以上が組み合わされて用いられてもよい。
As the component (C), cetyl alcohol and stearyl alcohol are preferred from the viewpoint of reducing the minor axis / major axis ratio of the glossy crystal.
These (C) components may be used alone or in combination of two or more.
光沢組成物中の(C)成分の含有量の下限値は、光沢組成物の総質量に対して、1質量%が好ましく、2質量%がより好ましく、3質量%がさらに好ましい。光沢組成物中の(C)成分の含有量の上限値は、光沢組成物の総質量に対して、10質量%が好ましく、6質量%がより好ましく、4質量%がさらに好ましい。即ち、光沢組成物中の(C)成分の含有量は、1質量%以上、10質量%以下が好ましく、2質量%以上、6質量%以下がより好ましく、3質量%以上、4質量%以下がさらに好ましい。上記下限値以上であれば、光沢結晶の短径/長径比をより小さくでき、上記上限値以下であれば、処理対象のべたつき感を抑えやすい。 The lower limit of the content of the component (C) in the gloss composition is preferably 1% by mass, more preferably 2% by mass, and still more preferably 3% by mass with respect to the total mass of the gloss composition. The upper limit of the content of the component (C) in the gloss composition is preferably 10% by mass, more preferably 6% by mass, and still more preferably 4% by mass with respect to the total mass of the gloss composition. That is, the content of the component (C) in the gloss composition is preferably 1% by mass or more and 10% by mass or less, more preferably 2% by mass or more and 6% by mass or less, and more preferably 3% by mass or more and 4% by mass or less. Is more preferable. If it is more than the said lower limit, the breadth / major axis ratio of a glossy crystal can be made smaller, and if it is below the said upper limit, it will be easy to suppress the sticky feeling of a process target.
光沢組成物中、(C)成分/(A)成分で表される質量比(以下、C/A比ということがある)は、0.2~1.5である。C/A比の下限値は、0.4が好ましく、0.6がより好ましい。C/A比の上限値は、1.3が好ましく、1.0がより好ましい。
即ち、光沢組成物中、(C)成分/(A)成分で表される質量比は、0.4以上、1.3以下が好ましく、0.6以上、1.0以下がより好ましい。
C/A比が上記下限値以上であれば、光沢結晶の短径/長径比をより小さくできる。上記上限値以下であれば、光沢結晶の短径/長径比をより小さくでき、処理対象のべたつき感を抑えやすい。
In the glossy composition, the mass ratio represented by component (C) / component (A) (hereinafter sometimes referred to as C / A ratio) is 0.2 to 1.5. The lower limit value of the C / A ratio is preferably 0.4, and more preferably 0.6. The upper limit value of the C / A ratio is preferably 1.3, and more preferably 1.0.
That is, in the glossy composition, the mass ratio represented by the component (C) / component (A) is preferably 0.4 or more and 1.3 or less, and more preferably 0.6 or more and 1.0 or less.
If the C / A ratio is not less than the above lower limit, the minor / major axis ratio of the glossy crystal can be further reduced. If it is below the upper limit, the minor axis / major axis ratio of the glossy crystal can be made smaller, and the stickiness of the object to be treated can be easily suppressed.
光沢組成物中、(B)成分/(C)成分で表される質量比(以下、B/C比ということがある)は、2~10が好ましく、4~8がより好ましい。上記下限値以上であれば、(C)成分が溶解しやすくなり、光沢結晶を製造しやすい、上記上限値以下であれば、光沢結晶の短径/長径比をより小さくできる。 In the gloss composition, the mass ratio represented by component (B) / component (C) (hereinafter sometimes referred to as B / C ratio) is preferably from 2 to 10, and more preferably from 4 to 8. If it is more than the said lower limit, (C) component will become easy to melt | dissolve and it will be easy to manufacture a glossy crystal, and if it is below the said upper limit, the minor axis / major axis ratio of a glossy crystal can be made smaller.
<水(D)>
光沢組成物は、水(D)(以下、(D)成分ということがある)を含有する。(D)成分は、主に光沢組成物の分散媒としての役割を有する。
光沢組成物中の水の含有量は、光沢組成物の総質量に対して、25~90質量%が好ましく、40~90質量%がより好ましく、50~80質量%がさらに好ましい。上記下限値未満では、流動性が損なわれて、取り扱いが煩雑になるおそれがあり、上記上限値超では、化粧料に十分な光沢を付与するために、光沢組成物の配合量を過度に高めなくてはならないおそれがある。
<Water (D)>
The glossy composition contains water (D) (hereinafter sometimes referred to as component (D)). The component (D) mainly serves as a dispersion medium for the gloss composition.
The content of water in the gloss composition is preferably 25 to 90% by mass, more preferably 40 to 90% by mass, and still more preferably 50 to 80% by mass with respect to the total mass of the gloss composition. If the amount is less than the above lower limit value, the fluidity may be impaired and handling may be complicated. If the amount exceeds the upper limit value, the amount of the gloss composition is excessively increased in order to impart sufficient gloss to the cosmetic. It may be necessary.
<芳香族カルボン酸又はその塩(E)>
光沢組成物は、芳香属カルボン酸又はその塩(E)(以下、(E)成分ということがある)を含有してもよい。(E)成分は、後述する光沢組成物の製造方法において、短径/長径比がより小さい光沢結晶を得られやすくする。
(E)成分を含有することで光沢結晶がより長くなり、かつ短径/長径比がより小さくなる理由は明らかではないが、以下のように推測される。
後述する光沢組成物の製造方法において、(E)成分は、(A)~(C)成分が乳化した乳化粒子に作用し、(D)成分に対する前記乳化粒子の溶解度を上げる。このため、混合物全体の過飽和度が低くなり、光沢結晶の核の過剰な析出が抑制される。光沢結晶の核の析出される数が少なくなると、微細な結晶同士の凝集が抑制され、長い光沢結晶に成長させやすくなると考えられる。
(E)成分としては、安息香酸、フタル酸、テレフタル酸、イソフタル酸、サリチル酸又はこれらの塩が好ましい。塩としては、アルカリ金属塩、アルカリ土類金属塩、アンモニウム塩、及びアルカノールアミン塩が好ましい。
<Aromatic carboxylic acid or salt thereof (E)>
The gloss composition may contain an aromatic carboxylic acid or a salt thereof (E) (hereinafter sometimes referred to as component (E)). The component (E) makes it easy to obtain glossy crystals having a smaller minor axis / major axis ratio in the method for producing a glossy composition described later.
The reason why the glossy crystal becomes longer and the minor axis / major axis ratio becomes smaller by containing the component (E) is not clear, but is presumed as follows.
In the method for producing a glossy composition described later, the component (E) acts on the emulsified particles obtained by emulsifying the components (A) to (C), and increases the solubility of the emulsified particles in the component (D). For this reason, the supersaturation degree of the whole mixture becomes low, and excessive precipitation of glossy crystal nuclei is suppressed. When the number of glossy crystal nuclei precipitated is reduced, aggregation of fine crystals is suppressed, and it is considered that it is easy to grow into a long glossy crystal.
As the component (E), benzoic acid, phthalic acid, terephthalic acid, isophthalic acid, salicylic acid or a salt thereof is preferable. As the salt, alkali metal salts, alkaline earth metal salts, ammonium salts, and alkanolamine salts are preferable.
光沢組成物中の(E)成分の含有量は、光沢組成物の総質量に対して、0.2~3質量%が好ましく、0.5~1.5質量%がより好ましい。上記下限値未満では、(E)成分の効果を得られにくく、上記上限値超では、光沢結晶が形成されにくくなる。
光沢組成物中、(A)成分/(E)成分で表される質量比(以下、A/E比ということがある)は、1~10が好ましく、3~6がより好ましい。上記下限値以上であれば、光沢結晶の短径/長径比をより小さくしやすく、上記上限値以下であれば、粗大な結晶の生成を抑制しやすい。
光沢組成物中、(B)成分/(E)成分で表される質量比(以下、B/E比ということがある)は、5~60が好ましく、10~30がより好ましい。B/E比が上記範囲内であれば、光沢結晶の短径/長径比をより小さくしやすい。
The content of the component (E) in the gloss composition is preferably 0.2 to 3% by mass and more preferably 0.5 to 1.5% by mass with respect to the total mass of the gloss composition. If it is less than the lower limit, it is difficult to obtain the effect of the component (E), and if it exceeds the upper limit, gloss crystals are hardly formed.
In the glossy composition, the mass ratio represented by component (A) / component (E) (hereinafter sometimes referred to as A / E ratio) is preferably 1 to 10, and more preferably 3 to 6. If it is at least the above lower limit value, it is easy to make the minor axis / major axis ratio of the glossy crystal smaller, and if it is at most the above upper limit value, it is easy to suppress the formation of coarse crystals.
In the glossy composition, the mass ratio represented by component (B) / component (E) (hereinafter sometimes referred to as B / E ratio) is preferably 5 to 60, and more preferably 10 to 30. If the B / E ratio is within the above range, it is easy to make the minor axis / major axis ratio of the glossy crystal smaller.
<光沢組成物のその他の任意成分>
光沢組成物は、(A)~(E)成分以外に、pH調整剤、(C)成分以外の1価のアルコール(任意アルコール)、ポリオール、防腐剤、塩類等の任意成分(光沢組成物用の任意成分)を含有してもよい。
pH調整剤としては、トリエタノールアミン、クエン酸等が挙げられる。光沢組成物は、pHが4.5~6.0であることが好ましい。
<Other optional components of the gloss composition>
In addition to the components (A) to (E), the gloss composition is a pH adjuster, a monovalent alcohol (arbitrary alcohol) other than the component (C), polyol, preservative, salts and other optional components (for gloss composition) Optional components).
Examples of the pH adjuster include triethanolamine and citric acid. The glossy composition preferably has a pH of 4.5 to 6.0.
(光沢組成物の製造方法)
 本発明の一実施形態である光沢組成物の製造方法は、(A)~(D)成分を(A)成分の融点以上で混合して混合物を得る混合工程と、前記混合物を晶析槽と冷却機とに循環させ冷却する晶析工程と、を含む。
(Glossy composition production method)
The method for producing a gloss composition according to an embodiment of the present invention comprises a mixing step of mixing the components (A) to (D) at a melting point or higher of the component (A) to obtain a mixture, and the mixture as a crystallization tank. A crystallization step of circulating and cooling to a cooler.
光沢組成物の製造方法について、以下に図1を参照して説明する。図1は、本発明の一実施形態である光沢組成物の製造装置(以下、単に製造装置ということがある)の一例を示す模式図である。
図1の製造装置1は、晶析機10と、冷却機20とを備える。晶析機10と冷却機20とは、第一の配管22と第二の配管26とで接続され、第一の配管22にはポンプ24が設けられている。
The manufacturing method of a glossy composition is demonstrated with reference to FIG. 1 below. FIG. 1 is a schematic diagram showing an example of a glossy composition production apparatus (hereinafter sometimes simply referred to as production apparatus) according to an embodiment of the present invention.
The manufacturing apparatus 1 in FIG. 1 includes a crystallizer 10 and a cooler 20. The crystallizer 10 and the cooler 20 are connected by a first pipe 22 and a second pipe 26, and a pump 24 is provided in the first pipe 22.
晶析機10は、晶析槽12と、晶析槽12内に設けられた攪拌翼14とを備える。
晶析槽12は、内部を任意の温度に調節できる晶析槽であればよく、例えば、ジャケット付の容器等が挙げられる。
冷却機20としては、例えば、液-液式熱交換器であるスパイラル式熱交換器、プレート式熱交換器、二重管式熱交換器、多管円筒式熱交換器、多重円管式熱交換器、渦巻管式熱交換器、渦巻板式熱交換器、タンクコイル式熱交換器、タンクジャケット式熱交換器、直接接触液液式熱交換器、気-液式熱交換器である空冷式熱交換器、直接接触気液式熱交換器、フィンチューブ熱交換器等が挙げられる。上記のなかでも、二重管式熱交換器、多管円筒式熱交換器、多重円管式熱交換器が好ましい。
ポンプ24としては、うず巻きポンプ、タービンポンプ、軸流ポンプ、斜流ポンプ等のターボ型ポンプ;ギアポンプ、直動蒸気ポンプ、プランジャーポンプ、ピストンポンプ等の定容量型ポンプ;噴流ポンプ、エアリフトポンプ、水撃ポンプ、ダイヤフラムポンプ等の特殊型ポンプ等が挙げられる。
The crystallizer 10 includes a crystallization tank 12 and a stirring blade 14 provided in the crystallization tank 12.
The crystallization tank 12 may be any crystallization tank whose inside can be adjusted to an arbitrary temperature, and examples thereof include a jacketed container.
Examples of the cooler 20 include a spiral heat exchanger, which is a liquid-liquid heat exchanger, a plate heat exchanger, a double tube heat exchanger, a multi-tube cylindrical heat exchanger, and a multi-tube heat Air-cooled type that is a heat exchanger, spiral tube heat exchanger, spiral plate heat exchanger, tank coil heat exchanger, tank jacket heat exchanger, direct contact liquid-liquid heat exchanger, gas-liquid heat exchanger A heat exchanger, a direct contact gas-liquid heat exchanger, a fin tube heat exchanger, etc. are mentioned. Among the above, a double tube heat exchanger, a multi-tube cylindrical heat exchanger, and a multiple tube heat exchanger are preferable.
The pump 24 includes a turbo pump such as a spiral pump, a turbine pump, an axial pump, and a mixed flow pump; a constant capacity pump such as a gear pump, a direct acting steam pump, a plunger pump, and a piston pump; a jet pump, an air lift pump, Special pumps such as water hammer pumps and diaphragm pumps are listed.
まず、(A)~(D)成分、及び必要に応じて光沢組成物用の任意成分((E)成分、pH調整剤、(C)成分以外の1価のアルコール(任意アルコール)、ポリオール、防腐剤、及び塩類からなる群から選択される少なくとも1つの成分)を晶析槽12に投入し、(A)成分の融点以上の温度に加熱しつつ、攪拌して混合物30を得る(混合工程)。 First, components (A) to (D) and, if necessary, optional components for the gloss composition (component (E), pH adjuster, monovalent alcohol (optional alcohol) other than component (C), polyol, (At least one component selected from the group consisting of preservatives and salts) is charged into the crystallization tank 12 and stirred to obtain a mixture 30 while being heated to a temperature equal to or higher than the melting point of the component (A) (mixing step). ).
混合工程における各成分の混合順序は特に限定されず、例えば、光沢組成物の製造に用いられる成分の全てを晶析槽12内に仕込み、これを(A)成分の融点以上の温度に加熱しつつ混合(一括混合法)してもよいし、各成分を晶析槽12に順次投入しつつ混合(分割混合法)してもよい。分割混合法としては、光沢組成物の製造に用いられる成分のうち、任意の成分を混合し(第一の混合操作)、次いで、第一の混合操作で使用しなかった残りの成分を混合する(第二の混合操作)方法が挙げられる。 The order of mixing the components in the mixing step is not particularly limited. For example, all the components used for the production of the gloss composition are charged into the crystallization tank 12 and heated to a temperature equal to or higher than the melting point of the component (A). The components may be mixed (collective mixing method) while mixing, or the components may be mixed (split mixing method) while being sequentially introduced into the crystallization tank 12. In the split mixing method, arbitrary components among the components used for the production of the gloss composition are mixed (first mixing operation), and then the remaining components not used in the first mixing operation are mixed. (Second mixing operation) method may be mentioned.
第一の混合操作は、例えば、(B)成分と(D)成分とを混合してもよいし、(A)成分と(B)成分と(D)成分とを混合してもよい。中でも、光沢結晶の短径/長径比をより小さくする観点からは、第一の混合操作は、(B)成分と(C)成分と(D)成分とを、(C)成分の融点以上の温度で、混合することが好ましい。即ち、分割混合法としては、(B)成分と(C)成分と(D)成分とを(C)成分の融点以上の温度で混合し、次いで、第二の混合操作で、(A)成分の融点以上の温度で(A)成分を前記第一の混合操作で得られた一次混合物に添加し、(A)成分の融点以上の温度で混合するのが好ましい。
第一の混合操作で(B)成分と(C)成分と(D)成分とを混合する場合、第二の混合操作では、(A)成分を予め(A)成分の融点以上の温度で溶融しておき、これを第一の混合操作で得られた(B)成分と(C)成分と(D)成分との一次混合物に添加し、(A)成分の融点以上の温度で混合するのが好ましい。 
In the first mixing operation, for example, the component (B) and the component (D) may be mixed, or the component (A), the component (B), and the component (D) may be mixed. Among these, from the viewpoint of reducing the minor axis / major axis ratio of the glossy crystal, the first mixing operation is carried out by adding the component (B), the component (C), and the component (D) above the melting point of the component (C). It is preferable to mix at a temperature. That is, as the split mixing method, the component (B), the component (C), and the component (D) are mixed at a temperature equal to or higher than the melting point of the component (C), and then the second mixing operation is performed. It is preferable to add the component (A) to the primary mixture obtained by the first mixing operation at a temperature equal to or higher than the melting point of the component (A) and to mix at a temperature equal to or higher than the melting point of the component (A).
When mixing the (B) component, the (C) component, and the (D) component in the first mixing operation, in the second mixing operation, the (A) component is previously melted at a temperature equal to or higher than the melting point of the (A) component. In addition, this is added to the primary mixture of the component (B), the component (C), and the component (D) obtained by the first mixing operation, and mixed at a temperature equal to or higher than the melting point of the component (A). Is preferred.
分割混合法において光沢組成物用の任意成分を配合する場合、光沢組成物用の任意成分の添加時期は、光沢組成物用の任意成分の種類等を勘案して決定される。
例えば、光沢組成物用の任意成分として(E)成分を用いる場合、(E)成分は、第一の混合操作で混合されることが好ましい。(E)成分が第一の混合操作で混合されることで、光沢結晶をより長くできる。
即ち、光沢組成物用の任意成分として(E)成分を用いる場合は、第一の混合操作は、(B)成分と(C)成分と(D)成分と(E)成分とを混合し、次いで、第二の混合操作で、(A)成分を、前記第一の混合操作で得られた一次混合物に添加し、混合するのが好ましい。
また、光沢組成物用の任意成分として(E)成分以外の任意成分も含む場合は、第一の混合操作は、(B)成分と(C)成分と(D)成分と(E)成分とを混合し、次いで、第二の混合操作で、(A)成分と(E)成分以外の任意成分とを溶融混合し、これを前記第一の混合操作で得られた一次混合物に添加し、混合するのが好ましい。
When blending the optional component for the gloss composition in the split mixing method, the addition timing of the optional component for the gloss composition is determined in consideration of the type of the optional component for the gloss composition.
For example, when the component (E) is used as an optional component for the gloss composition, the component (E) is preferably mixed in the first mixing operation. (E) A glossy crystal can be made longer because a component is mixed by 1st mixing operation.
That is, when the component (E) is used as an optional component for the gloss composition, the first mixing operation mixes the component (B), the component (C), the component (D), and the component (E), Subsequently, it is preferable to add and mix (A) component to the primary mixture obtained by said 1st mixing operation by 2nd mixing operation.
In addition, when an optional component other than the component (E) is also included as an optional component for the gloss composition, the first mixing operation includes the component (B), the component (C), the component (D), and the component (E). Then, in the second mixing operation, the components (A) and optional components other than the component (E) are melt-mixed, and this is added to the primary mixture obtained in the first mixing operation. It is preferable to mix.
混合工程における(A)成分の配合量は、光沢組成物の製造に用いられる全ての成分を混合した混合物の総質量(即ち、光沢組成物の製造に用いられる全ての成分の合計量)に対して、2~10質量%が好ましく、3~7質量%がより好ましく、4~6質量%がさらに好ましい。上記下限値未満では、光沢組成物中の光沢結晶の含有量が少なくなりすぎて、化粧料に十分な光沢を付与するために、光沢組成物の配合量を過度に高めなくてはならないおそれがある。
上記上限値超では、流動性が損なわれて取り扱いが煩雑になるおそれがある。
The blending amount of component (A) in the mixing step is based on the total mass of the mixture in which all the components used for producing the gloss composition are mixed (that is, the total amount of all the components used for producing the gloss composition). The content is preferably 2 to 10% by mass, more preferably 3 to 7% by mass, and still more preferably 4 to 6% by mass. If the amount is less than the lower limit, the content of the glossy crystal in the glossy composition is too small, and the blending amount of the glossy composition may have to be excessively increased in order to impart sufficient gloss to the cosmetic. is there.
If it exceeds the upper limit, the fluidity may be impaired and handling may be complicated.
混合工程における(B)成分の配合量は、光沢組成物の製造に用いられる全ての成分を混合した混合物の総質量(即ち、光沢組成物の製造に用いられる全ての成分の合計量)に対して、5~30質量%が好ましく、10~20質量%がより好ましい。上記下限値未満では、光沢結晶の短径/長径比を小さくしにくく、上記上限値超では、流動性が損なわれて取り扱いが煩雑になるおそれがある。 The blending amount of component (B) in the mixing step is based on the total mass of the mixture in which all the components used for producing the gloss composition are mixed (that is, the total amount of all the components used for producing the gloss composition). 5 to 30% by mass is preferable, and 10 to 20% by mass is more preferable. If the ratio is less than the lower limit, it is difficult to reduce the minor axis / major axis ratio of the glossy crystal. If the ratio exceeds the upper limit, the fluidity is impaired and handling may be complicated.
混合工程における(C)成分の配合量は、光沢組成物の製造に用いられる全ての成分を混合した混合物の総質量(即ち、光沢組成物の製造に用いられる全ての成分の合計量)に対して、1~10質量%が好ましく、2~6質量%がより好ましい。上記下限値以上であれば、光沢結晶の短径/長径比をより小さくでき、上記上限値以下であれば、処理対象のべたつき感を抑えやすい。 The blending amount of component (C) in the mixing step is based on the total mass of the mixture in which all the components used for producing the gloss composition are mixed (that is, the total amount of all the components used for producing the gloss composition). 1 to 10% by mass is preferable, and 2 to 6% by mass is more preferable. If it is more than the said lower limit, the breadth / major axis ratio of a glossy crystal can be made smaller, and if it is below the said upper limit, it will be easy to suppress the sticky feeling of a process target.
混合工程における(D)成分の配合量は、光沢組成物の製造に用いられる全ての成分を混合した混合物の総質量(即ち、光沢組成物の製造に用いられる全ての成分の合計量)に対して、25~90質量%が好ましく、40~90質量%がより好ましく、50~80質量%がさらに好ましい。
上記下限値未満では、流動性が損なわれて、取り扱いが煩雑になるおそれがあり、上記上限値超では、化粧料に十分な光沢を付与するために、光沢組成物の配合量を過度に高めなくてはならないおそれがある。
The blending amount of component (D) in the mixing step is based on the total mass of the mixture in which all components used for producing the gloss composition are mixed (that is, the total amount of all components used for producing the gloss composition). The content is preferably 25 to 90% by mass, more preferably 40 to 90% by mass, and still more preferably 50 to 80% by mass.
If the amount is less than the above lower limit value, the fluidity may be impaired and handling may be complicated. If the amount exceeds the upper limit value, the amount of the gloss composition is excessively increased in order to impart sufficient gloss to the cosmetic. It may be necessary.
光沢組成物用の任意成分として(E)成分を用いる場合、混合工程における(E)成分の配合量は、光沢組成物の製造に用いられる全ての成分を混合した混合物の総質量(即ち、光沢組成物の製造に用いられる全ての成分の合計量)に対して、0.2~3質量%が好ましく、0.5~1.5質量%がより好ましい。上記下限値未満では、(E)成分の効果を得られにくく、上記上限値超では、光沢結晶が形成されにくくなる。 When the component (E) is used as an optional component for the gloss composition, the blending amount of the component (E) in the mixing step is the total mass of the mixture in which all the components used for the production of the gloss composition are mixed (that is, the gloss The total amount of all components used in the production of the composition is preferably 0.2 to 3% by mass, more preferably 0.5 to 1.5% by mass. If it is less than the lower limit, it is difficult to obtain the effect of the component (E), and if it exceeds the upper limit, gloss crystals are hardly formed.
混合工程におけるA/B比は、0.1~0.5が好ましく、0.2~0.4がより好ましい。上記下限値以上であれば、後述する晶析工程において、光沢結晶を容易に析出でき、上記上限値以下であれば、微細な光沢結晶を得られやすい。混合工程におけるC/A比は、0.2~1.5である。C/A比の下限値は、0.4が好ましく、0.6がより好ましい。C/A比の上限値は、1.3が好ましく、1.0がより好ましい。即ち、C/A比は、0.4以上、1.3以下が好ましく、0.6以上、1.0以下がより好ましい。C/A比が上記下限値以上であれば、光沢結晶の短径/長径比をより小さくできる。上記上限値以下であれば、晶析工程における結晶の析出を制御しやすく、光沢結晶の短径/長径比をより小さくできる。
混合工程におけるB/C比は、2~10が好ましく、4~8がより好ましい。B/C比が上記下限値以上であれば、(C)成分が溶解しやすくなり、光沢結晶を製造しやすく、上記上限値以下であれば、光沢結晶の短径/長径比をより小さくできる。
混合工程におけるA/E比は、1~10が好ましく、3~6がより好ましい。A/E比が上記下限値以上であれば、光沢結晶の短径/長径比をより小さくしやすく、上記上限値以下であれば、粗大な結晶の生成を抑制しやすい。
混合工程におけるB/E比は、5~60が好ましく、10~30がより好ましい。B/E比が上記範囲内であれば、光沢結晶の短径/長径比をより小さくしやすい。
The A / B ratio in the mixing step is preferably from 0.1 to 0.5, more preferably from 0.2 to 0.4. If it is more than the said lower limit, a glossy crystal can be easily precipitated in the crystallization process mentioned later, and if it is below the said upper limit, it will be easy to obtain a fine glossy crystal. The C / A ratio in the mixing step is 0.2 to 1.5. The lower limit value of the C / A ratio is preferably 0.4, and more preferably 0.6. The upper limit value of the C / A ratio is preferably 1.3, and more preferably 1.0. That is, the C / A ratio is preferably 0.4 or more and 1.3 or less, and more preferably 0.6 or more and 1.0 or less. If the C / A ratio is not less than the above lower limit, the minor / major axis ratio of the glossy crystal can be further reduced. If it is below the upper limit, it is easy to control the precipitation of crystals in the crystallization step, and the minor axis / major axis ratio of the glossy crystals can be made smaller.
The B / C ratio in the mixing step is preferably from 2 to 10, and more preferably from 4 to 8. If the B / C ratio is equal to or higher than the lower limit, the component (C) is easily dissolved and a glossy crystal can be easily produced. If the B / C ratio is equal to or lower than the upper limit, the minor axis / major axis ratio of the glossy crystal can be further reduced. .
The A / E ratio in the mixing step is preferably 1 to 10, and more preferably 3 to 6. If the A / E ratio is not less than the above lower limit value, the minor axis / major axis ratio of the glossy crystal can be made smaller, and if it is not more than the above upper limit value, the formation of coarse crystals can be easily suppressed.
The B / E ratio in the mixing step is preferably 5 to 60, and more preferably 10 to 30. If the B / E ratio is within the above range, it is easy to make the minor axis / major axis ratio of the glossy crystal smaller.
混合工程における温度(混合温度)は、(A)成分の融点以上であり、(A)成分の融点よりも1~30℃高い温度が好ましく、(A)成分の融点よりも1~20℃高い温度がより好ましい。上記下限値未満では、光沢結晶の短径/長径比が大きくなり、かつ粗大になるおそれがあり、上記上限値超では、冷却時間が長くなり生産効率が低下するおそれがある。
加えて、混合温度は、(A)~(C)成分を溶融できる温度が好ましい。混合温度は、例えば、75~90℃が好ましく、75~85℃がより好ましい。
The temperature in the mixing step (mixing temperature) is equal to or higher than the melting point of the component (A), preferably 1 to 30 ° C. higher than the melting point of the component (A), and 1 to 20 ° C. higher than the melting point of the component (A). Temperature is more preferred. If the ratio is less than the lower limit, the ratio of the minor axis / major axis of the glossy crystal may be large and coarse, and if the ratio exceeds the upper limit, the cooling time may be long and the production efficiency may be reduced.
In addition, the mixing temperature is preferably a temperature at which the components (A) to (C) can be melted. For example, the mixing temperature is preferably 75 to 90 ° C, more preferably 75 to 85 ° C.
混合工程は、弱攪拌の条件で行われることが好ましい。混合工程が弱攪拌で行われることで、光沢結晶の短径/長径比を小さくしやすい。
本稿において「弱攪拌」とは、n/V=0.01~10となる条件である。混合工程の攪拌条件としては、n/V=0.05~5が好ましく、n/V=0.1~2がより好ましい。
/Vにおいて、nは攪拌翼の回転数(rpm)を示す。
dは攪拌翼の翼径(m)(図1のd1に相当)を示す
 なお、ここでいう「撹拌翼の翼径」とは、晶析槽を真上から見た際に、撹拌翼が外接する円における直径である。
Vは混合液の体積(m)を示す。
なお、混合工程において、攪拌翼14は、連続的に運転されてもよいし、間欠的に運転されてもよい。「間欠的に運転」とは、例えば起泡が激しい場合等などに脱泡する場合など、混合を途中で停止した後にまた再開するような運転が挙げられる。
The mixing step is preferably performed under weak stirring conditions. By performing the mixing step with weak stirring, the minor axis / major axis ratio of the glossy crystal can be easily reduced.
In this paper, “weak stirring” is a condition where n 3 d 5 /V=0.01 to 10. As the stirring condition in the mixing step, n 3 d 5 /V=0.05 to 5 is preferable, and n 3 d 5 /V=0.1 to 2 is more preferable.
In n 3 d 5 / V, n represents the rotation speed (rpm) of the stirring blade.
d indicates the blade diameter (m) of the stirring blade (corresponding to d1 in FIG. 1). Note that the “blade diameter of the stirring blade” here refers to the stirring blade when the crystallization tank is viewed from directly above. The diameter in the circumscribed circle.
V represents the volume (m 3 ) of the mixed solution.
In the mixing step, the stirring blade 14 may be operated continuously or intermittently. The “intermittent operation” includes an operation in which the mixing is stopped and then restarted again, for example, when defoaming occurs when foaming is severe.
即ち、本発明の一実施形態である光沢組成物の製造方法に係る混合工程の1つの側面は、
(A)~(D)成分、及び所望により光沢組成物用の任意成分((E)成分、pH調整剤、(C)成分以外の1価のアルコール(任意アルコール)、ポリオール、防腐剤、塩類からなる群から選択される少なくとも1つの成分)を晶析槽に投入し、混合温度で加熱しながら攪拌して混合物を得る混合工程であり;
前記混合工程は、
前記成分の全てを前記晶析槽内に仕込み、これを混合温度に加熱しながら混合する一括混合法で混合すること、又は、前記成分の全てを前記晶析槽に順次投入しながら混合温度で混合する分割混合法で混合することを含み;
前記分割混合法は、
(B)成分と(C)成分と(D)成分と、所望により(E)成分と、を混合して一次混合物を得る第一の混合操作と、
前記一次混合物に(A)成分及び所望により(E)以外の任意成分とを添加し混合する第二の混合操作と、を含む混合工程である。
前記混合温度は、(A)成分の融点以上が好ましい。
前記混合は、n/V=0.01~10である弱撹拌で、連続的又は間欠的に撹拌することにより行うことが好ましい。 
That is, one aspect of the mixing step according to the method for producing a glossy composition which is an embodiment of the present invention is:
Components (A) to (D), and optionally, optional components for gloss compositions (component (E), pH adjuster, monohydric alcohol (arbitrary alcohol) other than component (C)), polyols, preservatives, salts At least one component selected from the group consisting of: a crystallization tank and stirring while heating at the mixing temperature to obtain a mixture;
The mixing step includes
All of the components are charged into the crystallization tank and mixed by a batch mixing method in which the components are mixed while heating to the mixing temperature, or at the mixing temperature while all of the components are sequentially added to the crystallization tank. Including mixing by a split mixing method of mixing;
The split mixing method is:
A first mixing operation of mixing a component (B), a component (C), a component (D), and optionally a component (E) to obtain a primary mixture;
And a second mixing operation of adding and mixing the component (A) and an optional component other than the component (E) as required to the primary mixture.
The mixing temperature is preferably equal to or higher than the melting point of the component (A).
The mixing is preferably carried out by stirring continuously or intermittently with weak stirring where n 3 d 5 /V=0.01 to 10.
次いで、晶析槽12内の混合物30を上記混合温度で加熱するのを止め、ポンプ24を起動する。ポンプ24を起動すると、晶析槽12内の混合物30は、第一の配管22を経由して冷却機20に入る。冷却機20に入った混合物30は、冷却機20内を流通し、冷却される。冷却機20を流通した混合物30は、第二の配管26を経由して晶析槽12に戻る。こうして、晶析槽12内の混合物30は、晶析槽12と冷却機20とを循環する(晶析工程)。
このように、晶析槽12内の混合物30の一部を連続的に抜き出し、冷却機20で冷却し、晶析槽12に戻すことで、光沢結晶を析出させ、本発明の光沢組成物を得る。
Next, heating of the mixture 30 in the crystallization tank 12 at the mixing temperature is stopped, and the pump 24 is started. When the pump 24 is activated, the mixture 30 in the crystallization tank 12 enters the cooler 20 via the first pipe 22. The mixture 30 that has entered the cooler 20 flows through the cooler 20 and is cooled. The mixture 30 circulated through the cooler 20 returns to the crystallization tank 12 via the second pipe 26. Thus, the mixture 30 in the crystallization tank 12 circulates between the crystallization tank 12 and the cooler 20 (crystallization process).
Thus, a part of the mixture 30 in the crystallization tank 12 is continuously extracted, cooled by the cooler 20, and returned to the crystallization tank 12, thereby precipitating a glossy crystal and the gloss composition of the present invention. obtain.
冷却機20における冷却温度(即ち、冷却機(冷媒)の温度)は、(A)成分の凝固点以下の温度であり、(A)成分の凝固点よりも5~20℃低い温度が好ましく、(A)成分の凝固点よりも5~15℃低い温度が好ましい。冷却機20における冷却温度としては、例えば、10~40℃が挙げられる。上記下限値未満では、光沢結晶の短径/長径比が小さくなりにくく、上記上限値超では、微細な光沢結晶の凝集体が生成するおそれがある。冷却機20における冷却温度は、冷媒の温度を上記範囲内にする等して調節できる。 The cooling temperature in the cooler 20 (that is, the temperature of the cooler (refrigerant)) is a temperature not higher than the freezing point of the component (A), preferably 5 to 20 ° C. lower than the freezing point of the component (A). The temperature is preferably 5 to 15 ° C. lower than the freezing point of the component. Examples of the cooling temperature in the cooler 20 include 10 to 40 ° C. If the ratio is less than the above lower limit, the minor axis / major axis ratio of the glossy crystals is unlikely to be small, and if the ratio exceeds the upper limit, fine aggregates of glossy crystals may be generated. The cooling temperature in the cooler 20 can be adjusted by setting the temperature of the refrigerant within the above range.
冷却機20における冷却速度は、特に限定されない。例えば、冷却速度としては、晶析槽12内の混合物30を0.1~20℃/minで下げる条件が好ましく、晶析槽12内の混合物30を0.1~10℃/minで下げる条件がより好ましく、晶析槽12内の混合物30を0.1~5℃/minで下げる条件がさらに好ましい。上記下限値以上であれば、短時間で晶析できるため、光沢組成物の製造効率を高められ、上記上限値以下であれば、晶析温度が安定して、光沢結晶の短径/長径比を0.45未満にしやすい。 The cooling rate in the cooler 20 is not particularly limited. For example, the cooling rate is preferably a condition for lowering the mixture 30 in the crystallization tank 12 at 0.1 to 20 ° C./min, and a condition for lowering the mixture 30 in the crystallization tank 12 at 0.1 to 10 ° C./min. More preferably, the conditions for lowering the mixture 30 in the crystallization tank 12 at 0.1 to 5 ° C./min are more preferable. Since the crystallization can be performed in a short time if the above lower limit is exceeded, the production efficiency of the glossy composition can be improved. Of less than 0.45.
晶析工程における混合物30の循環速度は、晶析槽12内の混合物30の量や、冷却機20における冷却温度等を勘案して決定される。例えば、1分間当たり、混合物30の全量に対して0.01~0.5倍量を冷却機20に流通させ、晶析槽12に戻すことが好ましい。 The circulation speed of the mixture 30 in the crystallization step is determined in consideration of the amount of the mixture 30 in the crystallization tank 12, the cooling temperature in the cooler 20, and the like. For example, it is preferable that 0.01 to 0.5 times the amount of the mixture 30 per minute be passed through the cooler 20 and returned to the crystallization tank 12.
晶析工程の時間は、特に限定されず、晶析槽12内の混合物30が晶析終了温度に至る時点を晶析工程の終点とする。
晶析終了温度は、特に限定されず、(A)成分の凝固点以下であればよく、(A)成分の凝固点よりも5~40℃低い温度がより好ましく、(A)成分の凝固点よりも10~35℃低い温度がさらに好ましい。晶析終了温度は、例えば、10~45℃が好ましく、30~40℃がより好ましい。
冷却機20で冷却された混合物30が晶析槽12に戻されて、晶析槽12内の混合物30の温度が低下する。晶析槽内の混合物30の温度が低下して(A)成分の融点以下かつ凝固点以下になるまでに要する時間は、5~30分間が好ましく、10~20分間がより好ましい。上記範囲内であれば、微細で、短径/長径比がより小さい光沢結晶を得られやすい。
The time of the crystallization process is not particularly limited, and the time when the mixture 30 in the crystallization tank 12 reaches the crystallization end temperature is defined as the end point of the crystallization process.
The crystallization end temperature is not particularly limited, and may be any temperature below the freezing point of component (A), more preferably 5 to 40 ° C. lower than the freezing point of component (A), and 10 times higher than the freezing point of component (A). A temperature of ˜35 ° C. is more preferred. The crystallization end temperature is preferably, for example, 10 to 45 ° C, more preferably 30 to 40 ° C.
The mixture 30 cooled by the cooler 20 is returned to the crystallization tank 12, and the temperature of the mixture 30 in the crystallization tank 12 decreases. The time required for the temperature of the mixture 30 in the crystallization tank to fall below the melting point of the component (A) and below the freezing point is preferably 5 to 30 minutes, more preferably 10 to 20 minutes. If it is in the above-mentioned range, it is easy to obtain a glossy crystal that is fine and has a smaller minor axis / major axis ratio.
晶析工程の後、熟成工程を設けてもよい。熟成工程を設けることで、光沢結晶をさらに伸長させて、光沢結晶の短径/長径比をより小さくできる。
熟成工程は、光沢組成物を例えば、30~60℃の温度で2~24時間維持する工程である。
熟成方法としては、例えば、晶析工程と同様にして晶析槽12内の光沢組成物を冷却機20に流通さる方法、ポンプ24を停止し晶析槽12内を任意の温度に維持する方法、晶析槽12内の光沢組成物を他の容器に入れ、この容器を任意の温度で維持する方法等が挙げられる。熟成工程においては、光沢組成物を攪拌してもよいし、攪拌しなくてもよい。
ただし、光沢結晶を破砕しないようにする観点からは、攪拌しないことが好ましい。
熟成工程の温度(熟成温度)は、(A)成分の種類等を勘案して決定され、融点以下である。熟成温度は、例えば、30~60℃が好ましい。熟成温度が上記下限値以上であれば、光沢結晶の成長時間をより短縮でき、上記上限値以下であれば、結晶の成長速度を適正にして、短径/長径比を0.45未満にしやすい。
熟成工程の時間(熟成時間)は、所望する光沢結晶の短径/長径比等を勘案して決定され、例えば、2~24時間が好ましい。熟成時間が上記下限値以上であれば、光沢結晶を伸長させて、光沢結晶の短径/長径比をより小さくでき、上記上限値以下であれば、光沢結晶の長径が長くなりすぎるのを抑制し、破砕されにくくなる。
An aging step may be provided after the crystallization step. By providing the aging step, the glossy crystal can be further elongated, and the minor axis / major axis ratio of the glossy crystal can be further reduced.
The aging step is a step of maintaining the gloss composition at a temperature of 30 to 60 ° C. for 2 to 24 hours, for example.
As the aging method, for example, a method of circulating the glossy composition in the crystallization tank 12 to the cooler 20 in the same manner as the crystallization process, a method of stopping the pump 24 and maintaining the inside of the crystallization tank 12 at an arbitrary temperature. A method of putting the glossy composition in the crystallization tank 12 in another container and maintaining the container at an arbitrary temperature can be mentioned. In the aging step, the glossy composition may or may not be stirred.
However, from the viewpoint of preventing the lustrous crystals from being crushed, it is preferable not to stir.
The temperature of the aging step (aging temperature) is determined in consideration of the type of the component (A) and the like, and is below the melting point. The aging temperature is preferably 30 to 60 ° C., for example. If the aging temperature is not less than the above lower limit value, the growth time of the glossy crystal can be further shortened. .
The time of the ripening step (ripening time) is determined in consideration of the desired minor diameter / major diameter ratio of the glossy crystal and is preferably, for example, 2 to 24 hours. If the aging time is equal to or greater than the above lower limit value, the glossy crystal can be elongated to make the minor axis / major axis ratio of the glossy crystal smaller. And is less likely to be crushed.
 なお、上述の実施形態では、晶析機10で混合工程を行っているが、本発明はこれに限定されず、晶析機10以外の装置で混合物30を調製し、この混合物30を晶析槽12に投入してもよい。 In the above-described embodiment, the mixing step is performed by the crystallizer 10. However, the present invention is not limited to this, and the mixture 30 is prepared by an apparatus other than the crystallizer 10, and the mixture 30 is crystallized. You may throw into the tank 12.
即ち、本発明の一実施形態である光沢組成物の製造方法に係る晶析工程の1つの側面は、混合工程で得られた混合物を晶析槽と冷却機とに循環させ冷却する晶析工程であり;
前記冷却機における冷却温度は、(A)成分の凝固点よりも5~20℃低い温度であり、
前記晶析槽内における混合物の冷却速度は、0.1~20℃/minであり;
前記循環における循環速度は、1分間当たり、前記晶析槽内の混合物の全量に対して0.01~0.5倍量を前記冷却機に流通させて、前記晶析槽に戻す速度であり;
前記晶析工程の時間は、前記晶析槽内の混合物が晶析終了温度に至るまでである、晶析工程である。
前記晶析工程の時間は、5~30分間が好ましく、前記晶析終了温度は、(A)成分の凝固点よりも5~40℃低い温度が好ましい。
That is, one aspect of the crystallization process according to the method for producing a glossy composition which is an embodiment of the present invention is a crystallization process in which the mixture obtained in the mixing process is circulated between a crystallization tank and a cooler for cooling. Is;
The cooling temperature in the cooler is 5 to 20 ° C. lower than the freezing point of the component (A),
The cooling rate of the mixture in the crystallization tank is 0.1-20 ° C./min;
The circulation speed in the circulation is a speed at which 0.01 to 0.5 times the amount of the mixture in the crystallization tank per 1 minute is passed through the cooler and returned to the crystallization tank. ;
The time of the said crystallization process is a crystallization process which is until the mixture in the said crystallization tank reaches the crystallization completion temperature.
The crystallization step time is preferably 5 to 30 minutes, and the crystallization end temperature is preferably 5 to 40 ° C. lower than the freezing point of the component (A).
 本発明の一実施形態である光沢組成物の製造方法の1つの側面は、
(A)~(D)成分を(A)成分の融点以上で混合して混合物を得る混合工程と、前記混合物を晶析槽と冷却機とに循環させ冷却する晶析工程と、熟成工程と、を含む。
 前記熟成工程は、熟成温度が30~60℃が好ましく、熟成時間は2~24時間が好ましい。
One aspect of the manufacturing method of the glossy composition which is one embodiment of the present invention is:
A mixing step in which the components (A) to (D) are mixed at a melting point or higher of the component (A) to obtain a mixture, a crystallization step in which the mixture is circulated through a crystallization tank and a cooler, and a ripening step; ,including.
In the aging step, the aging temperature is preferably 30 to 60 ° C., and the aging time is preferably 2 to 24 hours.
冷却終了後に晶析槽より、移送熟成槽もしくは貯蔵槽に移送する。移送方法としては、移送先を低地にすることで重力を利用する方法や、ポンプ使用する。
ポンプとしては、結晶が破砕し短径/長径比が大きくならないように、比較的せん断の低いポンプ(ローターリーポンプ、モーノポンプ、ギアポンプ、サインポンプ等)が好ましい。
なお、晶析槽から貯槽、熟成槽から貯槽、もしくは晶析槽から熟成槽のいずれかに状況に応じて、結晶の凝集抑制や短径/長径比の制御の弊害となる異物を取り除くため濾過器を設置することが好ましい。濾過器の目開きとしては300μm以下の範囲で生産性を考慮して最も小さいものを選定することが好ましい。
熟成槽及び貯槽は必要に応じて加温・冷却可能な装置が選定される。
 貯槽から最終製品に添加混合されるが、その際には上記移送方法と同様のポンプを用い、配合槽の上面または液中に添加するが、光沢組成物に対して混合対象の途中工程品との粘度差が大きい場合には、渦巻ポンプ等の入側に添加する等の手段を用いて混合効率を向上させることが出来る。
 最終製品配合槽から製品貯蔵槽への移送についても上記のポンプや濾過装置を用いることが好ましい。
After cooling is completed, the sample is transferred from the crystallization tank to a transfer aging tank or storage tank. As a transfer method, a method of utilizing gravity by setting the transfer destination to a low ground or a pump is used.
As the pump, a pump having a relatively low shear (a rotary pump, a Mono pump, a gear pump, a sine pump, etc.) is preferable so that the crystal is not crushed and the ratio of the short axis / long axis is not increased.
Depending on the situation, either crystallization tank to storage tank, ripening tank to storage tank, or crystallization tank to aging tank, filtration is performed to remove foreign substances that are harmful to the control of crystal agglomeration and short / long diameter ratio control. It is preferable to install a vessel. As the opening of the filter, it is preferable to select the smallest one in consideration of productivity within a range of 300 μm or less.
For the aging tank and storage tank, a device capable of heating and cooling is selected as necessary.
It is added and mixed from the storage tank to the final product, and in that case, using the same pump as the above transfer method, it is added to the upper surface of the blending tank or in the liquid, When the difference in viscosity is large, the mixing efficiency can be improved by using means such as adding to the inlet side of a centrifugal pump or the like.
It is preferable to use the above-described pump and filtration device for transfer from the final product blending tank to the product storage tank.
(化粧料)
本発明の一実施形態である化粧料は、光沢組成物を含有する。
化粧料中の光沢組成物の含有量は、特に限定されないが、例えば、化粧料の総質量に対して、10~50質量%が好ましく、20~40質量%がより好ましく、30~40質量%がさらに好ましい。上記下限値未満では、化粧料の光沢が低下するおそれがあり、上記上限値超では、洗浄力や処理対象に与える質感等の化粧料の機能が低下するおそれがある。
化粧料は、光沢組成物以外に、シリコーン化合物(F)、カチオン性ポリマー(G)等を含有してもよい。
即ち、本発明の一実施形態である化粧料の1つの側面は、前記光沢組成物と、
シリコーン化合物(F)と、カチオン性ポリマー(G)と、所望により後述する化粧料任意成分と、を含む化粧料である。
(Cosmetics)
The cosmetic which is one embodiment of the present invention contains a gloss composition.
The content of the gloss composition in the cosmetic is not particularly limited, but is preferably 10 to 50% by mass, more preferably 20 to 40% by mass, and more preferably 30 to 40% by mass with respect to the total mass of the cosmetic. Is more preferable. If it is less than the lower limit, the gloss of the cosmetic may be lowered, and if it exceeds the upper limit, the function of the cosmetic such as a cleaning power or a texture to be treated may be lowered.
The cosmetic may contain a silicone compound (F), a cationic polymer (G) and the like in addition to the gloss composition.
That is, one aspect of the cosmetic according to an embodiment of the present invention includes the gloss composition,
A cosmetic comprising a silicone compound (F), a cationic polymer (G), and optional cosmetic ingredients described later if desired.
<シリコーン化合物(F)>
化粧料は、シリコーン化合物(F)(以下、(F)成分ということがある)と光沢組成物とを併有することで、すすぎ時のなめらかさを相乗的に高められる。加えて、(F)成分と光沢組成物とを併有するシャンプーやリンスは、洗浄後の頭髪のボリューム感等、処理対象の質感を相乗的に高められる。
(F)成分と光沢組成物とを併有することで、すすぎ時のなめらかさを相乗的に高めたり、処理対象の質感を相乗的に高められる理由は明らかではないが、以下のように推測される。
光沢組成物に含まれる光沢結晶は、短径/長径比0.45未満であり、細長い結晶である。このため、化粧料を用いて頭髪や皮膚等の処理対象を洗浄する際には、化粧料が水で希釈され、光沢結晶同士が絡み合って、網目状の構造物を形成する。この網目状の構造物は、比較的高い含水率であり、かつ網目状の構造内に(F)成分を取り込みやすく、(F)成分を取り込んだ網目状の構造物は、処理対象に付着しやすい。
このため、より多くの(F)成分が処理対象に付着し、処理対象をすすぐ際に、処理対象と手指との滑りがよくなって、すすぎ時のなめらかさを高められると考えられる。加えて、(F)成分を取り込んだ網目状の構造物は、頭髪を立体的に支えてボリューム感をより高められると考えられる。
<Silicone compound (F)>
The cosmetic composition synergistically increases the smoothness at the time of rinsing by having both the silicone compound (F) (hereinafter sometimes referred to as the component (F)) and the gloss composition. In addition, the shampoo and rinse containing both the component (F) and the gloss composition can synergistically enhance the texture of the object to be treated, such as the volume of the hair after washing.
The reason why the smoothness at the time of rinsing can be synergistically increased or the texture of the object to be processed can be synergistically increased by having both the component (F) and the gloss composition is not clear, but is estimated as follows. The
The glossy crystals contained in the glossy composition are elongated crystals having a minor axis / major axis ratio of less than 0.45. For this reason, when wash | cleaning processing objects, such as head hair and skin, using cosmetics, cosmetics are diluted with water and glossy crystals are intertwined and a mesh-like structure is formed. This network structure has a relatively high moisture content, and it is easy to incorporate the component (F) into the network structure. The network structure incorporating the component (F) adheres to the object to be treated. Cheap.
For this reason, it is considered that more (F) component adheres to the processing target, and when the processing target is rinsed, the slip between the processing target and the fingers is improved, and the smoothness at the time of rinsing can be improved. In addition, it is considered that the mesh-like structure incorporating the component (F) can support the hair three-dimensionally and enhance the volume feeling.
 (F)成分としては、従来、化粧料に配合されうる成分であればよく、例えば、ジメチルポリシロキサン(高重合ジメチルポリシロキサン、シリコーンゴムを含む)、メチルフェニルポリシロキサン、ポリエーテル変性シリコーン、ポリアミノ変性シリコーン、べタイン変性シリコーン、アルコール変性シリコーン、フッ素変性シリコーン、エポキシ変性シリコーン、メルカプト変性シリコーン、カルボキシ変性シリコーン、脂肪酸変性シリコーン、シリコーングラフトポリマー、環状シリコーン、アルキル変性シリコーン、トリメチルシリル基末端ジメチルポリシロキサン、シラノール基末端ジメチルポリシロキサン等が挙げられる。中でも、(F)成分としては、ジメチルポリシロキサン、ポリエーテル変性シリコーン、ポリアミノ変性シリコーンが好ましく、光沢組成物との相乗効果をより高める観点から、高重合ジメチルポリシロキサンがより好ましい。これらの(F)成分は、1種単独で用いられてもよいし、2種以上が組み合わされて用いられてもよい。
 (F)成分は、界面活性剤により乳化され、エマルション化された成分であってもよい。
The component (F) may be any component that can be conventionally blended in cosmetics, such as dimethylpolysiloxane (including highly polymerized dimethylpolysiloxane and silicone rubber), methylphenylpolysiloxane, polyether-modified silicone, polyamino. Modified silicone, betaine modified silicone, alcohol modified silicone, fluorine modified silicone, epoxy modified silicone, mercapto modified silicone, carboxy modified silicone, fatty acid modified silicone, silicone graft polymer, cyclic silicone, alkyl modified silicone, trimethylsilyl group terminated dimethylpolysiloxane, Examples thereof include silanol group-terminated dimethylpolysiloxane. Among them, as the component (F), dimethylpolysiloxane, polyether-modified silicone, and polyamino-modified silicone are preferable, and highly polymerized dimethylpolysiloxane is more preferable from the viewpoint of further enhancing the synergistic effect with the gloss composition. These (F) components may be used individually by 1 type, and may be used in combination of 2 or more type.
Component (F) may be a component emulsified and emulsified with a surfactant.
 高重合ジメチルポリシロキサンは、25℃における動粘度が500万mm/s以上のジメチルポリシロキサンである。
 高重合ジメチルポリシロキサンの動粘度は、800万mm/s以上が好ましい。動粘度の上限は、特に限定されないが、3000万mm/sが好ましい。
即ち、高重合ジメチルポリシロキサンの動粘度は、800万mm/s以上、3000万mm/s以下が好ましい。
The highly polymerized dimethylpolysiloxane is a dimethylpolysiloxane having a kinematic viscosity at 25 ° C. of 5 million mm 2 / s or more.
The kinematic viscosity of the highly polymerized dimethylpolysiloxane is preferably 8 million mm 2 / s or more. The upper limit of the kinematic viscosity is not particularly limited, but is preferably 30 million mm 2 / s.
That is, the kinematic viscosity of the highly polymerized dimethylpolysiloxane is preferably 8 million mm 2 / s or more and 30 million mm 2 / s or less.
動粘度は、以下の測定方法により測定された値である。
1g/100mL濃度のジメチルポリシロキサンのトルエン溶液(試料溶液)を調製し、下記式(1)により比粘度ηsp(25℃)を求める。
得られた比粘度ηspを下記式(2)に示すHugginsの関係式に代入し、固有粘度[η]を求める。Huggins定数は、『中牟田、「日本化学会誌」、77号、588頁、1956年』に記載の値を用いる。得られた[η]を下記式(3)に示すA.Kolorlovの式に代入し、ジメチルポリシロキサンの分子量Mを求める。得られたMを下記式(4)に示すA.J.Barryの式に代入し、ジメチルポリシロキサンの動粘度ηを求める。
ηsp=(η/η0)-1 ・・・(1)
((1)式中、η0はトルエンの粘度、ηは試料溶液の粘度を示す。)
ηsp=[η]+K’[η] ・・・(2)
((2)式中、K’はHugginsの定数である。)
[η]=0.215×10-40.65 ・・・(3)
((3)式中、Mはジメチルポリシロキサンの分子量である。)
logη=1.00+0.0123M0.5・・・(4)
((4)式中、Mはジメチルポリシロキサンの分子量である。)
上記のη0、ηは、化粧品原料基準、一般試験法、粘度測定法、第1法に準拠して測定される粘度である。
The kinematic viscosity is a value measured by the following measuring method.
A toluene solution (sample solution) of dimethylpolysiloxane having a concentration of 1 g / 100 mL is prepared, and the specific viscosity ηsp (25 ° C.) is obtained by the following formula (1).
The obtained specific viscosity ηsp is substituted into the Huggins relational expression shown in the following formula (2) to determine the intrinsic viscosity [η]. As the Huggins constant, a value described in “Nakamuta,“ Journal of the Chemical Society of Japan ”, No. 77, page 588, 1956” is used. The obtained [η] is represented by A. Substituting it into the Kololov equation, the molecular weight M of dimethylpolysiloxane is determined. The obtained M is represented by A. J. et al. Substituting into the Barry equation, the kinematic viscosity η of dimethylpolysiloxane is determined.
ηsp = (η / η0) −1 (1)
(In the formula (1), η0 represents the viscosity of toluene, and η represents the viscosity of the sample solution.)
ηsp = [η] + K ′ [η] 2 (2)
(In the formula (2), K ′ is a Huggins constant.)
[Η] = 0.215 × 10 −4 M 0.65 (3)
(In the formula (3), M is the molecular weight of dimethylpolysiloxane.)
log η = 1.00 + 0.0123M 0.5 (4)
(In the formula (4), M is the molecular weight of dimethylpolysiloxane.)
Said (eta) 0 and (eta) are the viscosity measured based on cosmetics raw material reference | standard, a general test method, a viscosity measuring method, and 1st method.
 高重合ジメチルポリシロキサンには、トリメチルシリル基末端ジメチルポリシロキサン、シラノール基末端ジメチルポリシロキサン等が含まれる。
 高重合ジメチルポリシロキサンは、1種単独で用いられてもよいし、2種以上が組み合わされて用いられてもよい。
The highly polymerized dimethylpolysiloxane includes trimethylsilyl group-terminated dimethylpolysiloxane, silanol group-terminated dimethylpolysiloxane, and the like.
The highly polymerized dimethylpolysiloxane may be used singly or in combination of two or more.
高重合ジメチルポリシロキサンの形態は、溶融した液体でもよいし、エマルションであってもよい。エマルション化における、乳化剤や乳化方法は、特に限定されない。 The form of the highly polymerized dimethylpolysiloxane may be a molten liquid or an emulsion. The emulsifier and emulsification method in emulsification are not particularly limited.
高重合ジメチルポリシロキサンの市販品としては、例えば、シリコーンエマルジョン(6)(一方社油脂工業株式会社製、動粘度=1000万mm/s、固形換算60質量%)、シリコーンエマルジョンKM-903(信越化学株式会社製、シリコーンオイルジメチルシリコ-ン、動粘度=2000万mm/s、固形換算60質量%)等が挙げられる。
化粧料中の(F)成分の含有量は、化粧料の種類等を勘案して決定される。例えば、化粧料がシャンプーであれば、シャンプー中の(F)成分の含有量は、シャンプーの総質量に対して、0.5~5質量%が好ましく、1~4質量%がより好ましい。上記下限値未満では、すすぎ時の滑らかさ、処理対象の質感が低下するおそれがあり、上記上限値超では、乾燥後の頭髪のべたつきが大きくなるおそれがある。
Commercially available products of highly polymerized dimethylpolysiloxane include, for example, silicone emulsion (6) (manufactured by Yushi Kogyo Co., Ltd., kinematic viscosity = 10 million mm 2 / s, solid conversion 60% by mass), silicone emulsion KM-903 ( Silicone oil dimethyl silicone manufactured by Shin-Etsu Chemical Co., Ltd., kinematic viscosity = 20 million mm 2 / s, solid conversion 60% by mass) and the like.
The content of the component (F) in the cosmetic is determined in consideration of the type of cosmetic. For example, when the cosmetic is a shampoo, the content of the component (F) in the shampoo is preferably 0.5 to 5% by mass and more preferably 1 to 4% by mass with respect to the total mass of the shampoo. If it is less than the above lower limit value, the smoothness during rinsing and the texture of the object to be treated may be reduced, and if it exceeds the above upper limit value, the stickiness of the hair after drying may be increased.
化粧料中、(A)成分/(F)成分で表される質量比(以下、A/F比ということがある)は、化粧料の種類等を勘案して決定される。例えば、化粧料がシャンプーであれば、A/F比は0.06~60が好ましく、0.2~40がより好ましく、1~20がさらに好ましい。上記下限値未満では、(F)成分によるすすぎ時の滑らかさが低下するおそれがあり、上記上限値超では、乾燥後の頭髪のべたつきが大きくなるおそれがある。 In cosmetics, the mass ratio represented by component (A) / component (F) (hereinafter sometimes referred to as A / F ratio) is determined in consideration of the type of cosmetics and the like. For example, if the cosmetic is a shampoo, the A / F ratio is preferably 0.06 to 60, more preferably 0.2 to 40, and even more preferably 1 to 20. If it is less than the lower limit, the smoothness during rinsing with the component (F) may be reduced, and if it exceeds the upper limit, stickiness of the hair after drying may be increased.
<カチオン性ポリマー(G)>
化粧料は、カチオン性ポリマー(G)(以下、(G)成分ということがある)と光沢組成物とを併有することで、すすぎ時のなめらかさを相乗的に高められる。加えて、(G)成分と光沢組成物とを併有するシャンプーやリンスは、洗浄後の頭髪のボリューム感等の処理対象の質感を相乗的に高められる。
(G)成分と光沢組成物とを併有することで、すすぎ時のなめらかさを相乗的に高めたり、処理対象の質感を相乗的に高められる理由は明らかではないが、以下のように推測される。
化粧料を用いて頭髪や皮膚等の処理対象を洗浄する際には、化粧料が水で希釈され、光沢結晶同士が絡み合って、網目状の構造物を形成する。この網目状の構造物は、比較的高い含水率であり、かつ網目状の構造内に(G)成分を取り込みやすく、(G)成分を取り込んだ網目状の構造物は、処理対象に付着しやすい。
このため、より多くの(G)成分が処理対象に付着した状態となり、処理対象をすすぐ際に、処理対象と手指との滑りがよくなって、すすぎ時のなめらかさを高められると考えられる。加えて、(G)成分を取り込んだ網目状の構造物は、頭髪を立体的に支えてボリューム感をより高められると考えられる。
<Cationic polymer (G)>
The cosmetic can synergistically increase the smoothness during rinsing by having both the cationic polymer (G) (hereinafter sometimes referred to as the component (G)) and the gloss composition. In addition, the shampoo and rinse containing both the component (G) and the gloss composition can synergistically enhance the texture of the treatment target such as the volume of hair after washing.
The reason why the smoothness at the time of rinsing can be increased synergistically or the texture of the object to be processed can be increased synergistically by having both the component (G) and the gloss composition is not clear, but is estimated as follows. The
When a treatment target such as hair or skin is washed using the cosmetic, the cosmetic is diluted with water, and the glossy crystals are entangled to form a network structure. This network structure has a relatively high water content, and it is easy to incorporate the component (G) into the network structure. The network structure incorporating the component (G) adheres to the object to be treated. Cheap.
For this reason, it is considered that more (G) components are attached to the processing target, and when the processing target is rinsed, the slip between the processing target and the fingers is improved, and the smoothness at the time of rinsing can be increased. In addition, it is considered that the mesh-like structure incorporating the component (G) can enhance the volume feeling by supporting the hair three-dimensionally.
(G)成分としては、従来、化粧料に配合されうる成分であればよく、例えば、カチオン化セルロース、カチオン化グァーガム、塩化ジメチルジアリルアンモニウム・アクリルアミド共重合体、カチオン化デキストラン、カチオン化プルラン等が挙げられる。中でも、光沢組成物との相乗効果をより高める観点から、カチオン化グァーガム、塩化ジメチルジアリルアンモニウム・アクリルアミド共重合体が好ましい。 The component (G) may be any component that can be blended in cosmetics, and examples thereof include cationized cellulose, cationized guar gum, dimethyldiallylammonium chloride / acrylamide copolymer, cationized dextran, and cationized pullulan. Can be mentioned. Of these, cationized guar gum and dimethyldiallylammonium chloride / acrylamide copolymer are preferred from the viewpoint of further enhancing the synergistic effect with the gloss composition.
化粧料中の(G)成分の含有量は、化粧料の種類等を勘案して決定される。例えば、化粧料がシャンプーであれば、シャンプー中の(G)成分の含有量は、シャンプーの総質量に対して、0.01~5質量%が好ましく、0.1~2質量%がより好ましい。上記下限値未満では、すすぎ時の滑らかさ、処理対象の質感が低下するおそれがあり、上記上限値超では、すすぎ時にぬるつきやすくなるおそれがある。 The content of the component (G) in the cosmetic is determined in consideration of the type of cosmetic. For example, when the cosmetic is a shampoo, the content of the component (G) in the shampoo is preferably 0.01 to 5% by mass and more preferably 0.1 to 2% by mass with respect to the total mass of the shampoo. . If it is less than the above lower limit value, the smoothness at the time of rinsing and the texture of the object to be processed may be reduced, and if it exceeds the above upper limit value, it may be easily wet during the rinsing.
化粧料中、(A)成分/(G)成分で表される質量比(以下、A/G比ということがある)は、化粧料の種類等を勘案して決定される。例えば、化粧料がシャンプーであれば、A/G比は0.2~2000が好ましく、5~200がより好ましい。上記下限値未満では、すすぎ時の滑らかさが低下するおそれがあり、上記上限値超では、乾燥後の頭髪のべたつきが大きくなるおそれがある。 In cosmetics, the mass ratio represented by component (A) / component (G) (hereinafter sometimes referred to as A / G ratio) is determined in consideration of the type of cosmetics and the like. For example, if the cosmetic is a shampoo, the A / G ratio is preferably 0.2 to 2000, more preferably 5 to 200. If it is less than the lower limit, the smoothness during rinsing may be reduced, and if it exceeds the upper limit, stickiness of the hair after drying may be increased.
<化粧料のその他の任意成分>
化粧料は、必要に応じ、光沢組成物及び(F)~(G)成分以外の任意成分(以下、化粧料任意成分ということがある)を含有してもよい。
化粧料任意成分としては、界面活性剤;アニオン性ポリマー、ノニオン性ポリマー等、(F)成分及び(G)成分以外のポリマー(任意ポリマー);ポリオール類;食塩、芒硝等の無機塩類;有機塩類;プロピレングリコール等の保湿剤;トニック剤;可溶化剤;BHTやα-トコフェロール等の酸化防止剤;トリクロサン、トリクロロカルバン等の殺菌剤;脂肪酸モノエタノールアミド、脂肪酸ジエタノールアミド等の粘度調整剤;紫外線吸収剤;酸化防止剤;タンパク誘導体;動植物抽出液;ピロクトンオラミン、ジンクピリチオン等のフケ防止剤;グリチルリチン酸ジカリウム等の抗炎症剤;安息香酸及びその塩、パラベン類、ケーソンCG等の防腐剤;クエン酸、トリエタノールアミン等のpH調整剤;乳濁剤;ビタミン類;揮発性油分;色素;香料;水等が挙げられる。
<Other optional ingredients in cosmetics>
The cosmetic may contain optional components other than the gloss composition and the components (F) to (G) (hereinafter sometimes referred to as cosmetic optional components) as necessary.
Cosmetic optional ingredients include surfactants; anionic polymers, nonionic polymers, etc., polymers other than (F) and (G) ingredients (arbitrary polymers); polyols; inorganic salts such as salt and salt cake; organic salts Humectants such as propylene glycol; tonic agents; solubilizers; antioxidants such as BHT and α-tocopherol; bactericides such as triclosan and trichlorocarban; viscosity modifiers such as fatty acid monoethanolamide and fatty acid diethanolamide; Absorbents; Antioxidants; Protein derivatives; Animal and plant extracts; Antidandruff agents such as piroctone olamine and zinc pyrithione; Anti-inflammatory agents such as dipotassium glycyrrhizinate; ; PH adjusters such as citric acid and triethanolamine; Emulsifiers; Vitamins; Volatile Min; dyes; perfumes; water and the like.
化粧料任意成分の界面活性剤としては、(B)成分と同様の成分が挙げられる。
化粧料任意成分の任意ポリマーとしては、ペクチン、カラギーナン、グァーガム、ローカストビーンガム、ゼラチン、キサンタンガム、カルボキシビニルポリマー、カルボキシメチルヒドロキシエチルセルロース、ヒドロキシエチルセルロース、ヒドロキシプロピルメチルセルロース、アルギン酸塩、デンプン、ポリビニルアルコール、ポリアクリル酸塩、ポリメタクリル酸塩、ポリメチルアクリル酸塩、ポリエチレングリコール、ポリエチレンオキシド、トラガラントゴム等が挙げられる。
Examples of the surfactant as a cosmetic optional component include the same components as the component (B).
Optional polymers for cosmetic ingredients include pectin, carrageenan, guar gum, locust bean gum, gelatin, xanthan gum, carboxyvinyl polymer, carboxymethylhydroxyethylcellulose, hydroxyethylcellulose, hydroxypropylmethylcellulose, alginate, starch, polyvinyl alcohol, polyacrylic Examples include acid salts, polymethacrylates, polymethyl acrylates, polyethylene glycols, polyethylene oxides, and tragarant rubbers.
配合される化粧料任意成分の種類は、化粧料に求める機能等を勘案して適宜決定される。
化粧料中の化粧料任意成分の含有量は、化粧料任意成分の種類等を勘案して適宜決定される。
The type of cosmetic optional ingredients to be blended is appropriately determined in consideration of functions required for cosmetics.
The content of the cosmetic optional ingredient in the cosmetic is appropriately determined in consideration of the type of cosmetic optional ingredient.
(化粧料の製造方法)
化粧料の製造方法としては、特に限定されず、例えば、水等の分散媒に、光沢組成物、(F)~(G)成分及び必要に応じて化粧料任意成分を分散する方法が挙げられる。分散媒への各成分の添加順序は、特に限定されない。
なお、ここでいう「分散」とは、各成分が分散媒の中で沈降していない状態になることを意味する。
(Cosmetics production method)
The method for producing the cosmetic is not particularly limited, and examples thereof include a method of dispersing the gloss composition, the components (F) to (G) and optional cosmetic ingredients in a dispersion medium such as water. . The order of adding each component to the dispersion medium is not particularly limited.
Here, “dispersion” means that each component does not settle in the dispersion medium.
 上述の通り、本発明の光沢組成物は、(A)成分を含有する光沢結晶と、(B)~(D)成分とを含み、光沢結晶の短径/長径比が0.45未満で、C/A比が特定の範囲であるため、化粧料に良好な光沢を与え、かつ化粧料におけるすすぎ時のなめらかさと処理対象の質感とをより高められる。 As described above, the gloss composition of the present invention comprises gloss crystals containing the component (A) and the components (B) to (D), and the minor crystal / major axis ratio of the gloss crystals is less than 0.45, Since the C / A ratio is in a specific range, the cosmetic is given a good gloss, and the smoothness of the cosmetic during rinsing and the texture of the treatment target can be further enhanced.
本発明の一実施形態である光沢組成物のその他の態様としては、
下記一般式(I)で表される脂肪酸グリコールエステル(A)を含有する結晶と、界面活性剤(B)と、炭素数8~22のアルコール(C)と、水(D)とを含み;
 前記(C)成分/前記(A)成分で表される質量比が0.2~1.5であり、
前記結晶の短径/長径で表される比は、0.10以上、0.45未満である光沢組成物であり;
前記光沢組成物の総質量に対して、
前記(A)成分が、2質量%以上、10質量%以下であり、
前記(B)成分が、5質量%以上、30質量%以下であり、
前記(C)成分が、1質量%以上、10質量%以下であり、
前記(D)成分が、25~90質量%であり、かつ
前記各成分の合計量が100質量%を超えない光沢用組成物が挙げられる。
 Y-O-(RO)-CO-R ・・・(I)
 ((I)式中、Rは、炭素数13~21の炭化水素基を表し;Rは、炭素数2~4のアルキレン基を表し;mは、(RO)の平均繰り返し数を表す1~3の数であり;Yは、水素原子又はRCO-を表し;Rは、炭素数13~21の炭化水素基を表す。)
As other aspects of the gloss composition which is one embodiment of the present invention,
A crystal containing a fatty acid glycol ester (A) represented by the following general formula (I), a surfactant (B), an alcohol having 8 to 22 carbon atoms (C), and water (D);
The mass ratio represented by the component (C) / the component (A) is 0.2 to 1.5,
The ratio represented by the minor axis / major axis of the crystal is a gloss composition having a ratio of 0.10 or more and less than 0.45;
With respect to the total mass of the gloss composition,
The component (A) is 2% by mass or more and 10% by mass or less,
The component (B) is 5% by mass or more and 30% by mass or less,
The component (C) is 1% by mass or more and 10% by mass or less,
Examples include a gloss composition in which the component (D) is 25 to 90% by mass and the total amount of the components does not exceed 100% by mass.
Y—O— (R 2 O) m —CO—R 1 (I)
(In the formula (I), R 1 represents a hydrocarbon group having 13 to 21 carbon atoms; R 2 represents an alkylene group having 2 to 4 carbon atoms; m represents an average number of repetitions of (R 2 O)) Y represents a hydrogen atom or R 3 CO—; R 3 represents a hydrocarbon group having 13 to 21 carbon atoms.)
本発明の一実施形態である光沢組成物のその他の態様としては、
前記一般式(I)で表される脂肪酸グリコールエステル(A)を含有する結晶と、界面活性剤(B)と、炭素数8~22のアルコール(C)と、水(D)と、芳香族カルボン酸又はその塩(E)と、所望により任意成分と、を含み;
前記(C)成分/前記(A)成分で表される質量比が0.2~1.5であり;
 前記結晶の短径/長径で表される比は、0.10以上、0.45未満である光沢組成物であり;
前記光沢組成物の総質量に対して、
前記(A)成分が、2質量%以上、10質量%以下であり、
前記(B)成分が、5質量%以上、30質量%以下であり、
前記(C)成分が、1質量%以上、10質量%以下であり、
前記(D)成分が、25~90質量%であり、
前記(E)成分が、0.2~3質量%であり、かつ
前記各成分の合計量が100質量%を超えない光沢用組成物が挙げられる。
As other aspects of the gloss composition which is one embodiment of the present invention,
Crystals containing the fatty acid glycol ester (A) represented by the general formula (I), a surfactant (B), an alcohol (C) having 8 to 22 carbon atoms, water (D), and an aromatic A carboxylic acid or a salt thereof (E) and, optionally, an optional component;
The mass ratio represented by the component (C) / component (A) is 0.2 to 1.5;
The ratio represented by the minor axis / major axis of the crystal is a gloss composition having a ratio of 0.10 or more and less than 0.45;
With respect to the total mass of the gloss composition,
The component (A) is 2% by mass or more and 10% by mass or less,
The component (B) is 5% by mass or more and 30% by mass or less,
The component (C) is 1% by mass or more and 10% by mass or less,
The component (D) is 25 to 90% by mass,
Examples include a gloss composition in which the component (E) is 0.2 to 3% by mass and the total amount of the components does not exceed 100% by mass.
本発明の一実施形態である光沢組成物のその他の態様としては、
(A)ジステアリン酸エチレングリコール、を含有する結晶と、
(B)陰イオン性界面活性剤と、
(C)ラウリルアルコール、ミリスチルアルコール、セチルアルコール、ステアリルアルコール、及びベヘニルアルコールからなる群から選択される少なくとも1つのアルコールと、
(D)水と、
(E)安息香酸、フタル酸、テレフタル酸、イソフタル酸、サリチル酸又はこれらの塩と、
所望により任意成分と、を含み;
  前記(C)成分/前記(A)成分で表される質量比が0.2~1.5であり; 
 前記結晶の短径/長径で表される比は、0.10以上、0.45未満である光沢組成物であり;
前記光沢組成物の総質量に対して、
前記(A)成分が、2質量%以上、10質量%以下であり、
前記(B)成分が、5質量%以上、30質量%以下であり、
前記(C)成分が、1質量%以上、10質量%以下であり、
前記(D)成分が、25~90質量%であり、
前記(E)成分が、0.2~3質量%であり、かつ
前記各成分の合計量が100質量%を超えない光沢用組成物が挙げられる。
As other aspects of the gloss composition which is one embodiment of the present invention,
(A) crystals containing ethylene glycol distearate;
(B) an anionic surfactant;
(C) at least one alcohol selected from the group consisting of lauryl alcohol, myristyl alcohol, cetyl alcohol, stearyl alcohol, and behenyl alcohol;
(D) water,
(E) benzoic acid, phthalic acid, terephthalic acid, isophthalic acid, salicylic acid or a salt thereof;
Optionally containing optional ingredients;
The mass ratio represented by the component (C) / component (A) is 0.2 to 1.5;
The ratio represented by the minor axis / major axis of the crystal is a gloss composition having a ratio of 0.10 or more and less than 0.45;
With respect to the total mass of the gloss composition,
The component (A) is 2% by mass or more and 10% by mass or less,
The component (B) is 5% by mass or more and 30% by mass or less,
The component (C) is 1% by mass or more and 10% by mass or less,
The component (D) is 25 to 90% by mass,
Examples include a gloss composition in which the component (E) is 0.2 to 3% by mass and the total amount of the components does not exceed 100% by mass.
本発明の一実施形態である化粧料のその他の態様としては、
 光沢組成物と、シリコーン化合物(F)と、カチオン性ポリマー(G)と、分散媒と、所望により化粧料任意成分と、を含み;
前記光沢組成物は、前述の本発明の光沢組成物であり、
(F)成分は、ジメチルポリシロキサン、ポリエーテル変性シリコーン、及びポリアミノ変性シリコーンからなる群から選択される少なくとも1つであり、
(G)成分は、カチオン化グァーガム、及び塩化ジメチルジアリルアンモニウム・アクリルアミド共重合体からなる群から選択される少なくとも1つであり;
前記光沢組成物の総質量に対して、
前記(A)成分が、2質量%以上、10質量%以下であり、
前記(B)成分が、5質量%以上、30質量%以下であり、
前記(C)成分が、1質量%以上、10質量%以下であり;
前記化粧料の総質量に対して、
(F)の含有量は、0.5~5質量%であり、
(G)の含有量は、0.01~5質量%であり;
(A)成分/(F)成分で表される質量比は、0.06~60であり、
(A)成分/(G)成分で表される質量比は、0.2~2000である、
化粧料が挙げられる。
As other aspects of the cosmetic that is one embodiment of the present invention,
A gloss composition, a silicone compound (F), a cationic polymer (G), a dispersion medium, and optionally a cosmetic optional component;
The gloss composition is the gloss composition of the present invention described above,
The component (F) is at least one selected from the group consisting of dimethylpolysiloxane, polyether-modified silicone, and polyamino-modified silicone,
Component (G) is at least one selected from the group consisting of cationized guar gum and dimethyldiallylammonium chloride-acrylamide copolymer;
With respect to the total mass of the gloss composition,
The component (A) is 2% by mass or more and 10% by mass or less,
The component (B) is 5% by mass or more and 30% by mass or less,
The component (C) is 1% by mass or more and 10% by mass or less;
For the total mass of the cosmetic,
The content of (F) is 0.5 to 5% by mass,
The content of (G) is 0.01 to 5% by mass;
The mass ratio represented by component (A) / component (F) is 0.06 to 60,
The mass ratio represented by component (A) / component (G) is 0.2 to 2000.
Examples include cosmetics.
本発明の一実施形態である化粧料のその他の態様としては、
 光沢組成物と、シリコーン化合物(F)と、カチオン性ポリマー(G)と、分散媒と、所望により化粧料任意成分と、を含み;
前記光沢組成物は、前述の本発明の光沢組成物であり、
(F)成分は、高重合ジメチルポリシロキサンであり、
(G)成分は、カチオン化グァーガム、及び塩化ジメチルジアリルアンモニウム・アクリルアミド共重合体からなる群から選択される少なくとも1つであり、
前記化粧料任意成分は、界面活性剤、香料、クエン酸からなる群から選択される少なくとも1つを含み;
前記光沢組成物の総質量に対して、
前記(A)成分が、2質量%以上、10質量%以下であり、
前記(B)成分が、5質量%以上、30質量%以下であり、
前記(C)成分が、1質量%以上、10質量%以下であり;
前記化粧料の総質量に対して、
(F)の含有量は、0.5~5質量%であり、
(G)の含有量は、0.01~5質量%であり;
(A)成分/(F)成分で表される質量比は、0.06~60であり、
(A)成分/(G)成分で表される質量比は、0.2~2000である、
化粧料が挙げられる。
As other aspects of the cosmetic that is one embodiment of the present invention,
A gloss composition, a silicone compound (F), a cationic polymer (G), a dispersion medium, and optionally a cosmetic optional component;
The gloss composition is the gloss composition of the present invention described above,
(F) component is highly polymerized dimethylpolysiloxane,
The component (G) is at least one selected from the group consisting of cationized guar gum and dimethyldiallylammonium chloride / acrylamide copolymer,
The cosmetic optional ingredient includes at least one selected from the group consisting of a surfactant, a fragrance, and citric acid;
With respect to the total mass of the gloss composition,
The component (A) is 2% by mass or more and 10% by mass or less,
The component (B) is 5% by mass or more and 30% by mass or less,
The component (C) is 1% by mass or more and 10% by mass or less;
For the total mass of the cosmetic,
The content of (F) is 0.5 to 5% by mass,
The content of (G) is 0.01 to 5% by mass;
The mass ratio represented by component (A) / component (F) is 0.06 to 60,
The mass ratio represented by component (A) / component (G) is 0.2 to 2000.
Examples include cosmetics.
 以下、実施例を示して本発明を詳細に説明するが、本発明は以下の記載によって限定されるものではない。 Hereinafter, the present invention will be described in detail with reference to examples, but the present invention is not limited to the following description.
(使用原料)
<(A)成分>
A-1:ジステアリン酸エチレングリコール(Genapol PMS(商品名)、クラリアントジャパン株式会社製、融点70℃、凝固点56℃)。
(Raw material)
<(A) component>
A-1: Ethylene glycol distearate (Genapol PMS (trade name), manufactured by Clariant Japan, melting point 70 ° C., freezing point 56 ° C.).
<(B)成分>
B-1:ポリオキシエチレン(平均3モル)ラウリルエーテル硫酸アンモニウム(Texapon ALES 70(商品名)、コグニスジャパン株式会社製、純分70質量%)。
B-2:ラウリル硫酸アンモニウム(Texapon ALSIS T(商品名)、コグニスジャパン株式会社製)。
B-3:ポリオキシエチレン(平均2モル)ラウリルエーテル硫酸ナトリウム(シノリンSPE-1250(商品名)、新日本理化株式会社製、純分70質量%)。
<(B) component>
B-1: Polyoxyethylene (average 3 mol) ammonium lauryl ether sulfate (Texapon ALES 70 (trade name), manufactured by Cognis Japan, pure content 70% by mass).
B-2: Ammonium lauryl sulfate (Texapon ALICS T (trade name), manufactured by Cognis Japan Co., Ltd.).
B-3: Polyoxyethylene (average 2 moles) sodium lauryl ether sulfate (Sinoline SPE-1250 (trade name), manufactured by Shin Nippon Rika Co., Ltd., pure content: 70% by mass).
<(C)成分>
C-1:ラウリルアルコール(コノール20P(商品名)、新日本理化式会社製、融点23℃)。
C-2:セチルアルコール(LANETTE 16(商品名)、コグニスジャパン株式会社製、融点50℃)。
C-3:ステアリルアルコール(LANETTE 18(商品名)、コグニスジャパン株式会社製、融点60℃)。
C-4:ベヘニルアルコール(LANETTE 22(商品名)、コグニスジャパン株式会社製、融点75℃)。
<(C) component>
C-1: Lauryl alcohol (Conol 20P (trade name), manufactured by Shin Nippon Chemical Co., Ltd., melting point 23 ° C.).
C-2: Cetyl alcohol (LANETTE 16 (trade name), manufactured by Cognis Japan, melting point 50 ° C.).
C-3: Stearyl alcohol (LANETTE 18 (trade name), manufactured by Cognis Japan, melting point 60 ° C.).
C-4: Behenyl alcohol (LANETTE 22 (trade name), manufactured by Cognis Japan, melting point 75 ° C.).
<(D)成分>
D-1:精製水。
<(D) component>
D-1: Purified water.
<(E)成分>
E-1:安息香酸ナトリウム(安息香酸ソーダ(商品名)、BFGoodrich Kalama Inc.製)。
<(E) component>
E-1: Sodium benzoate (sodium benzoate (trade name), manufactured by BFGoodrich Kalama Inc.).
<(F)成分>
F-1:高重合ジメチルシリコーン(シリコーンエマルジョン(6)(商品名)、一方社油脂工業株式会社製、エマルション、純分60質量%)。
<(F) component>
F-1: Highly polymerized dimethyl silicone (silicone emulsion (6) (trade name), manufactured by Yushi Kogyo Co., Ltd., emulsion, pure content 60 mass%).
<(G)成分>
G-1:カチオン化グァーガム(ラボールガムCG-M6L(商品名)、大日本製薬株式会社製)。
G-2:塩化ジメチルジアリルアンモニウム・アクリルアミド共重合体(カヤクリルレジンM-50(商品名)、日本化薬株式会社製)。
<(G) component>
G-1: Cationized guar gum (Labor gum CG-M6L (trade name), manufactured by Dainippon Pharmaceutical Co., Ltd.).
G-2: Dimethyldiallylammonium chloride / acrylamide copolymer (Kayacrill Resin M-50 (trade name), manufactured by Nippon Kayaku Co., Ltd.).
<化粧料任意成分>
≪界面活性剤≫
ポリオキシエチレン(平均2モル)ラウリルエーテル硫酸ナトリウム(シノリンSPE-1250(商品名)、新日本理化株式会社製、純分70質量%)。表中、POE(2)ラウリルエーテル硫酸ナトリウムと記載。
ポリオキシエチレン(平均3モル)ラウリン酸モノエタノールアミド(アミゼット2L-Y(商品名)、川研ファインケミカル株式会社製)。表中、POE(3)ラウリン酸モノエタノールアミドと記載。
ラウリン酸アミドプロピルベタイン(LPB-30(商品名)、一方社油脂工業株式会社製)。
ポリオキシエチレン(平均20モル)硬化ヒマシ油(CW-20-90(商品名)、青木油脂工業株式会社製)。表中、POE(20)硬化ヒマシ油と記載。
<Cosmetics optional ingredients>
≪Surfactant≫
Polyoxyethylene (2 mol on average) sodium lauryl ether sulfate (Sinoline SPE-1250 (trade name), manufactured by Shin Nippon Chemical Co., Ltd., pure content: 70% by mass). In the table, described as POE (2) sodium lauryl ether sulfate.
Polyoxyethylene (average 3 mol) lauric acid monoethanolamide (Amidette 2L-Y (trade name), manufactured by Kawaken Fine Chemical Co., Ltd.). In the table, described as POE (3) lauric acid monoethanolamide.
Lauric acid amidopropyl betaine (LPB-30 (trade name), manufactured by Yushi Kogyo Co., Ltd.).
Polyoxyethylene (average 20 mol) hydrogenated castor oil (CW-20-90 (trade name), manufactured by Aoki Oil & Fat Co., Ltd.). In the table, described as POE (20) hydrogenated castor oil.
≪その他≫
香料(特開2006-63044号公報の表5~10に記載の香料B)。
クエン酸(扶桑化学工業株式会社製)。
≪Others≫
Perfume (perfume B described in Tables 5 to 10 of JP-A-2006-63044).
Citric acid (manufactured by Fuso Chemical Industries).
(評価方法)
<短径/長径比の測定>
各例の光沢組成物を精製水で5倍に希釈して、これを試料とした。得られた試料について、位相差光学顕微鏡(AX70、オリンパス株式会社製)を用いて観察(倍率40倍)した。5視野からそれぞれ2個ずつ、計10個の光沢結晶を無作為に選択し、この短径/長径比を求めた。表中には、10個の光沢結晶の短径の平均値、長径の平均値及び短径/長径比の平均値を記載した。
(Evaluation methods)
<Measurement of ratio of minor axis / major axis>
The gloss composition of each example was diluted 5 times with purified water and used as a sample. About the obtained sample, it observed (magnification 40 times) using the phase-contrast optical microscope (AX70, Olympus Corporation). A total of 10 glossy crystals, 2 each from 5 fields of view, were selected at random, and the ratio of the minor axis / major axis was determined. In the table, the average value of the minor axis, the average value of the major axis, and the average value of the minor axis / major axis ratio of 10 glossy crystals are described.
<外観(光沢)>
各例のシャンプーを目視で観察し、パール様の光沢があるものを「A」、パール様の光沢がないものを「B」と評価した。
<Appearance (Glossy)>
The shampoos in each example were visually observed, and those having a pearly luster were evaluated as “A”, and those having no pearly luster were evaluated as “B”.
<すすぎ時のなめらかさ>
10人の被験者が、頭髪を左右に分け、その片方を下記の標準試料3gで洗髪し、他方を各例のシャンプー3gで洗髪した。各例のシャンプーで洗髪した際の感触を下記評価基準に従って評価し、10人の評価点を合算した。評価点の合計が高いほど、すすぎ時のなめらかさに優れるといえる。
<Smoothness when rinsing>
Ten test subjects divided their hair left and right, and one of them was washed with 3 g of the following standard sample, and the other was washed with 3 g of the shampoo of each example. The feel when the hair was washed with the shampoo of each example was evaluated according to the following evaluation criteria, and 10 evaluation points were added up. It can be said that the higher the total score, the better the smoothness during rinsing.
≪標準試料の組成≫
・ポリオキシエチレン(平均3モル)ラウリルエーテル硫酸アンモニウム:標準試料の総質量に対して15質量%。
・ヤシ油脂肪酸アミドプロピルベタイン(アミゾールCME(商品名)、川研ファインケミカル株式会社製):標準試料の総質量に対して3質量%。
・ヤシ油脂肪酸ジエタノールアミド(CDE100(川研ファインケミカル株式会社製)):標準試料の総質量に対して1.5質量%。
・香料(特開2006-63044号公報の表5~10に記載の香料B):標準試料の総質量に対して0.4質量%。
・クエン酸(扶桑化学工業株式会社製):標準試料をpH6に調整するのに必要な量。
・精製水:バランス(標準試料を100質量%にするのに必要な量)。
<Composition of standard sample>
Polyoxyethylene (average 3 mol) ammonium lauryl ether sulfate: 15% by mass relative to the total mass of the standard sample.
Palm oil fatty acid amidopropyl betaine (Amizole CME (trade name), manufactured by Kawaken Fine Chemical Co., Ltd.): 3% by mass relative to the total mass of the standard sample.
Coconut oil fatty acid diethanolamide (CDE100 (manufactured by Kawaken Fine Chemical Co., Ltd.)): 1.5% by mass relative to the total mass of the standard sample.
Fragrance (fragrance B described in Tables 5 to 10 of JP-A-2006-63044): 0.4% by mass relative to the total mass of the standard sample.
Citric acid (manufactured by Fuso Chemical Industry Co., Ltd.): The amount necessary to adjust the standard sample to pH 6.
-Purified water: Balance (amount required to make the standard sample 100% by mass).
≪評価基準≫
+3点:標準試料に比べて、非常になめらかである。
+2点:標準試料に比べて、なめらかである。
+1点:標準試料に比べて、ややなめらかである。
0点:標準試料と同等である。
-1点:標準試料の方が、ややなめらかである。
-2点:標準試料の方が、なめらかである。
-3点:標準試料の方が、非常になめらかである。
≪Evaluation criteria≫
+3 points: Very smooth compared to the standard sample.
+2 points: Smoother than the standard sample.
+1 point: Slightly smoother than the standard sample.
0 point: equivalent to a standard sample.
-1 point: The standard sample is slightly smoother.
-2 points: The standard sample is smoother.
-3 points: The standard sample is much smoother.
<頭髪のボリューム感>
「<すすぎ時のなめらかさ>」と同様にして、10人の被験者が洗髪した。各例のシャンプーで洗髪した際の感触を下記評価基準に従って評価した。10人の評価点を合算した。評価点の合計が高いほど、頭髪のボリューム感に優れるといえる。
<Volume of hair>
10 subjects washed their hair in the same manner as “<smoothness during rinsing>”. The feel when the hair was washed with the shampoo of each example was evaluated according to the following evaluation criteria. The evaluation score of 10 people was added up. It can be said that the higher the total score, the better the volume of hair.
≪評価基準≫
+3点:標準試料に比べて、非常にボリューム感がある。
+2点:標準試料に比べて、ボリューム感がある。
+1点:標準試料に比べて、ややボリューム感がある。
0点:標準試料と同等である。
-1点:標準試料の方が、ややボリューム感がある。
-2点:標準試料の方が、ボリューム感がある。
-3点:標準試料の方が、非常にボリューム感がある。
≪Evaluation criteria≫
+3 points: There is a very voluminous feel compared to the standard sample.
+2 points: There is a volume feeling compared to the standard sample.
+1 point: There is a little volume compared to the standard sample.
0 point: equivalent to a standard sample.
-1 point: The standard sample has a slightly voluminous feel.
-2 points: The standard sample has a volume feeling.
-3 points: The standard sample is much more voluminous.
(実施例1-1~1-10、比較例1-2~1-3)
表1~2に従い、以下の手順で各例の光沢組成物600gを調製した。各例の光沢組成物は、環境温度25℃の条件下で調製されたものである。表中の各成分の配合量は、純分換算量である(以降において同じ)。
晶析槽である1Lビーカーに(B)成分、(C)成分、(D)成分及び(E)成分を入れ、これを加熱して表中の混合温度に調整しつつ、スリーワンモータ(FBL1200、HEIDON社製)で20分間混合した(第一の混合操作)。(B)成分、(C)成分、(D)成分及び(E)成分との一次混合物に(A)成分を添加して二次混合物とした。マイクロポンプ(型番184-405、株式会社中央理化製)を用い、二次混合物をビーカーとラインホモミキサー(ROBOMIX f-model、Primix社製、攪拌条件:4500rpm)とに、25g/minで10分間循環させて、混合物を得た(第二の混合操作。以上、混合工程。)。この時点で、混合物を加熱するのを止めた。
マイクロポンプ(型番184-405、株式会社中央理化製)を用い、ビーカー内の混合物をビーカーと冷却機(アルミニウム製のスパイラル式熱交換器)とに、25g/minで循環させた。冷却機の冷却温度(冷媒の温度)を表中の「冷却温度」の通りとした。
ビーカー内の混合物が表中の「晶析終了温度」になるまで、混合物をビーカーと冷却機とに循環して、光沢組成物P1~P10、P’2~P’3を得た(晶析工程)。表中、本例の晶析方法を「循環」と記載した。
得られた光沢組成物について、光沢結晶の短径/長径比を測定した。
(Examples 1-1 to 1-10, Comparative Examples 1-2 to 1-3)
According to Tables 1 and 2, 600 g of the gloss composition of each example was prepared by the following procedure. The gloss composition in each example was prepared under the condition of an environmental temperature of 25 ° C. The compounding amount of each component in the table is a pure conversion amount (the same applies hereinafter).
While putting (B) component, (C) component, (D) component and (E) component into a 1 L beaker which is a crystallization tank, and adjusting this to the mixing temperature in the table, three one motor (FBL1200, (Made by HEIDON) for 20 minutes (first mixing operation). (A) component was added to the primary mixture with (B) component, (C) component, (D) component, and (E) component, and it was set as the secondary mixture. Using a micropump (model number 184-405, manufactured by Chuo Rika Co., Ltd.), the secondary mixture was placed in a beaker and a line homomixer (ROBOMIX f-model, manufactured by Primix, stirring condition: 4500 rpm) at 25 g / min for 10 minutes. The mixture was circulated to obtain a mixture (second mixing operation, mixing step). At this point, heating of the mixture was stopped.
Using a micropump (model number 184-405, manufactured by Chuo Rika Co., Ltd.), the mixture in the beaker was circulated at a rate of 25 g / min between the beaker and a cooler (aluminum spiral heat exchanger). The cooling temperature of the cooler (refrigerant temperature) was set as “Cooling temperature” in the table.
The mixture was circulated through the beaker and the cooler until the mixture in the beaker reached the “crystallization end temperature” in the table, and gloss compositions P1 to P10 and P′2 to P′3 were obtained (crystallization). Process). In the table, the crystallization method of this example was described as “circulation”.
About the obtained glossy composition, the minor axis / major axis ratio of the glossy crystals was measured.
(実施例1-11)
晶析工程の後、光沢組成物を48℃の恒温槽内に放置した(熟成工程)以外は、実施例1-1と同様にして、光沢組成物P11を得た。熟成時間は、表中に示した通りである。
得られた、光沢組成物について、光沢結晶の短径/長径比を測定した。
(Example 1-11)
After the crystallization step, a glossy composition P11 was obtained in the same manner as in Example 1-1 except that the glossy composition was left in a constant temperature bath at 48 ° C. (aging step). The aging time is as shown in the table.
About the obtained glossy composition, the minor axis / major axis ratio of the glossy crystals was measured.
(比較例1-1)
晶析工程を以下の通りとした以外は、実施例1-1と同様にして光沢組成物を得た。
ビーカー内の混合物をマイクロポンプで冷却機に1回流通させて、光沢組成物P’1を得た(晶析工程)。この際、冷却機の出口における混合物の温度が35℃となるように、混合物の流量を調整した。熟成工程は、実施例1-1と同じ条件である。得られた光沢組成物について、光沢結晶の短径/長径比を測定した。表中、本例の晶析方法を「ワンパス」と記載した。
(Comparative Example 1-1)
A glossy composition was obtained in the same manner as in Example 1-1 except that the crystallization process was as follows.
The mixture in the beaker was passed through the cooler once with a micro pump to obtain a glossy composition P′1 (crystallization step). At this time, the flow rate of the mixture was adjusted so that the temperature of the mixture at the outlet of the cooler was 35 ° C. The aging process is under the same conditions as in Example 1-1. About the obtained glossy composition, the minor axis / major axis ratio of the glossy crystals was measured. In the table, the crystallization method of this example was described as “one pass”.
Figure JPOXMLDOC01-appb-T000001
Figure JPOXMLDOC01-appb-T000001
Figure JPOXMLDOC01-appb-T000002
Figure JPOXMLDOC01-appb-T000002
表1~2に示す通り、本発明を適用した実施例1-1~1-11は、光沢結晶の短径/長径比が0.45未満であった。
一方、晶析工程をワンパス式で行った比較例1-1、(B)成分又は(C)成分を含有しない比較例1-2~1-3は、いずれも光沢結晶の短径/長径比が0.45以上であった。
As shown in Tables 1 and 2, in Examples 1-1 to 1-11 to which the present invention was applied, the minor crystal / major axis ratio of the glossy crystals was less than 0.45.
On the other hand, Comparative Example 1-1, in which the crystallization process was performed by a one-pass method, and Comparative Examples 1-2 to 1-3 not containing component (B) or (C), all had a minor axis / major axis ratio of glossy crystals. Was 0.45 or more.
図2は実施例1-1で得られた光沢組成物P1の顕微鏡写真(倍率40倍)であり、図3は実施例1-11で得られた光沢組成物P11の顕微鏡写真(倍率40倍)である。図4は比較例1-1で得られた光沢組成物P’1の顕微鏡写真(倍率40倍)である。
図2~3に示すように、光沢組成物P1及び光沢組成物P11の光沢結晶は、短径/長径比が小さい針状であった。
図4に示すように、光沢組成物P’1の光沢結晶は、短径/長径比が大きかった。
FIG. 2 is a photomicrograph of the glossy composition P1 obtained in Example 1-1 (magnification 40 times), and FIG. 3 is a photomicrograph of the glossy composition P11 obtained in Example 1-11 (magnification 40 times). ). FIG. 4 is a photomicrograph (magnification 40 times) of the glossy composition P′1 obtained in Comparative Example 1-1.
As shown in FIGS. 2 to 3, the glossy crystals of the glossy composition P1 and the glossy composition P11 were needle-like with a minor axis / major axis ratio.
As shown in FIG. 4, the glossy crystal of the glossy composition P′1 had a large minor axis / major axis ratio.
(実施例2-1~2-11、比較例2-1~2-3)
表3~4に従い、200mLビーカーに、光沢組成物及びクエン酸を除く各成分を入れ、25℃で30分間攪拌した。光沢組成物を加え、10分間攪拌した後、クエン酸でpH6に調整して、各例のシャンプー100gを得た。得られたシャンプーについて、外観、すすぎ時のなめらかさ、頭髪のボリューム感を評価し、その結果を表中に示す。
各例に用いた光沢組成物は、実施例1-1~1-11、比較例1-1~1-3で得られた光沢組成物P1~P11、P’1~P’3である。
表中、クエン酸の配合量である「適量」は、シャンプーをpH6にするのに要した量を示し、シャンプーの総質量に対して、0.8~1.3質量%である。表中、精製水の配合量である「バランス」は、シャンプーを100質量%とするのに必要な量を示す。
(Examples 2-1 to 2-11, Comparative Examples 2-1 to 2-3)
According to Tables 3 to 4, each component except the glossy composition and citric acid was placed in a 200 mL beaker and stirred at 25 ° C. for 30 minutes. The gloss composition was added and stirred for 10 minutes, and then adjusted to pH 6 with citric acid to obtain 100 g of each shampoo. About the obtained shampoo, the appearance, the smoothness at the time of rinsing, and the volume of hair were evaluated, and the results are shown in the table.
The gloss compositions used in each example are the gloss compositions P1 to P11 and P′1 to P′3 obtained in Examples 1-1 to 1-11 and Comparative Examples 1-1 to 1-3.
In the table, “suitable amount” which is the blending amount of citric acid indicates the amount required to bring the shampoo to pH 6, and is 0.8 to 1.3% by mass relative to the total mass of the shampoo. In the table, “balance”, which is the blending amount of purified water, indicates the amount required to make the shampoo 100% by mass.
Figure JPOXMLDOC01-appb-T000003
Figure JPOXMLDOC01-appb-T000003
Figure JPOXMLDOC01-appb-T000004
Figure JPOXMLDOC01-appb-T000004
表3~4に示すように、本発明を適用した実施例2-1~2-11は、いずれもパール様の光沢があり、すすぎ時のなめらかさの評価が12点以上、頭髪のボリューム感の評価が12点以上であった。
光沢結晶の短径/長径比が0.45以上である光沢組成物を用いた比較例2-1~2-3は、パール様の光沢があるものの、すすぎ時のなめらかさが-10点以下であり、頭髪のボリューム感が-12点以下であった。
これらの結果から、本発明を適用することで、化粧料にパール様の光沢を付与し、かつ化粧料におけるすすぎ時のなめらかさと処理対象の質感とをより高められることが判った。
As shown in Tables 3 to 4, each of Examples 2-1 to 2-11 to which the present invention was applied had a pearly luster, an evaluation of smoothness at the time of rinsing of 12 points or more, and the volume of hair. The evaluation was 12 points or more.
Comparative Examples 2-1 to 2-3 using a glossy composition having a minor axis / major axis ratio of 0.45 or more of glossy crystals have a pearly luster, but have a smoothness of -10 points or less when rinsed. The volume of hair was -12 points or less.
From these results, it was found that by applying the present invention, a pearly luster was imparted to the cosmetic, and the smoothness at the time of rinsing in the cosmetic and the texture of the treatment object could be further enhanced.
 本発明の光沢組成物によれば、化粧料にパール様の光沢を付与し、かつ化粧料におけるすすぎ時のなめらかさと処理対象の質感とをより高められるので、産業上極めて重要である。 According to the gloss composition of the present invention, a pearly luster is imparted to the cosmetic, and the smoothness of the cosmetic during rinsing and the texture of the treatment object can be further enhanced, which is extremely important in industry.
 1 光沢組成物の製造装置
 10 晶析機
 12 晶析槽
 20 冷却機
 30 混合物
DESCRIPTION OF SYMBOLS 1 Manufacturing apparatus of gloss composition 10 Crystallizer 12 Crystallization tank 20 Cooling machine 30 Mixture

Claims (4)

  1.  下記一般式(I)で表される脂肪酸グリコールエステル(A)を含有する結晶と、
    界面活性剤(B)と、
    炭素数8~22のアルコール(C)と、
    水(D)とを含み;
      前記(C)成分/前記(A)成分で表される質量比が0.2~1.5であり;
     前記結晶の短径/長径で表される比は、0.45未満である
     光沢組成物。
     Y-O-(RO)-CO-R ・・・(I)
     ((I)式中、Rは、炭素数13~21の炭化水素基を表し、Rは、炭素数2~4のアルキレン基を表し、mは、(RO)の平均繰り返し数を表す1~3の数である。Yは、水素原子又はRCO-を表し、Rは、炭素数13~21の炭化水素基を表す。)
    A crystal containing a fatty acid glycol ester (A) represented by the following general formula (I);
    A surfactant (B),
    Alcohol (C) having 8 to 22 carbon atoms;
    Including water (D);
    The mass ratio represented by the component (C) / component (A) is 0.2 to 1.5;
    The ratio represented by the minor axis / major axis of the crystal is less than 0.45.
    Y—O— (R 2 O) m —CO—R 1 (I)
    (In the formula (I), R 1 represents a hydrocarbon group having 13 to 21 carbon atoms, R 2 represents an alkylene group having 2 to 4 carbon atoms, and m represents an average number of repetitions of (R 2 O). Y represents a hydrogen atom or R 3 CO—, and R 3 represents a hydrocarbon group having 13 to 21 carbon atoms.)
  2. さらに、芳香族カルボン酸又はその塩(E)を含む請求項1に記載の光沢組成物。 Furthermore, the glossy composition of Claim 1 containing aromatic carboxylic acid or its salt (E).
  3. 請求項1又は2に記載の光沢組成物を含有する化粧料。 A cosmetic comprising the gloss composition according to claim 1 or 2.
  4.  晶析槽と冷却機とを備えた製造装置を用いる請求項1に記載の光沢組成物の製造方法であって、
     前記製造装置は、前記晶析槽と前記冷却機とが接続されており、
     前記製造方法は、
    前記(A)~(D)成分を前記(A)成分の融点以上で混合して混合物を得る混合工程と、
     前記混合物を前記晶析槽と前記冷却機とに循環させて、前記(A)成分の凝固点以下の温度に冷却し、前記(A)成分を含有する結晶を析出させる晶析工程と、
     を含む光沢組成物の製造方法。
    The method for producing a glossy composition according to claim 1, wherein a production apparatus comprising a crystallization tank and a cooler is used.
    In the manufacturing apparatus, the crystallization tank and the cooler are connected,
    The manufacturing method includes:
    A mixing step of mixing the components (A) to (D) above the melting point of the component (A) to obtain a mixture;
    A crystallization step in which the mixture is circulated through the crystallization tank and the cooler, cooled to a temperature not higher than the freezing point of the component (A), and crystals containing the component (A) are precipitated;
    A method for producing a glossy composition comprising:
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