WO2022176825A1 - セルロースアシレート組成物及びその製造方法 - Google Patents
セルロースアシレート組成物及びその製造方法 Download PDFInfo
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- WO2022176825A1 WO2022176825A1 PCT/JP2022/005803 JP2022005803W WO2022176825A1 WO 2022176825 A1 WO2022176825 A1 WO 2022176825A1 JP 2022005803 W JP2022005803 W JP 2022005803W WO 2022176825 A1 WO2022176825 A1 WO 2022176825A1
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- Prior art keywords
- cellulose acylate
- particles
- less
- metal compound
- plasticizer
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- 229920002678 cellulose Polymers 0.000 title claims abstract description 191
- 239000001913 cellulose Substances 0.000 title claims abstract description 191
- ODIGIKRIUKFKHP-UHFFFAOYSA-N (n-propan-2-yloxycarbonylanilino) acetate Chemical compound CC(C)OC(=O)N(OC(C)=O)C1=CC=CC=C1 ODIGIKRIUKFKHP-UHFFFAOYSA-N 0.000 title claims abstract description 184
- 239000000203 mixture Substances 0.000 title claims abstract description 94
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- 238000006467 substitution reaction Methods 0.000 claims abstract description 31
- 150000001339 alkali metal compounds Chemical class 0.000 claims abstract description 13
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- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims description 16
- 125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 claims description 16
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 claims description 15
- 239000000243 solution Substances 0.000 claims description 14
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- 125000002252 acyl group Chemical group 0.000 claims description 12
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- 125000004063 butyryl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 6
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- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 4
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- 238000007865 diluting Methods 0.000 description 1
- XTDYIOOONNVFMA-UHFFFAOYSA-N dimethyl pentanedioate Chemical compound COC(=O)CCCC(=O)OC XTDYIOOONNVFMA-UHFFFAOYSA-N 0.000 description 1
- KWABLUYIOFEZOY-UHFFFAOYSA-N dioctyl butanedioate Chemical compound CCCCCCCCOC(=O)CCC(=O)OCCCCCCCC KWABLUYIOFEZOY-UHFFFAOYSA-N 0.000 description 1
- RXJJVYBGRFLCOX-UHFFFAOYSA-N dioctyl pentanedioate Chemical compound CCCCCCCCOC(=O)CCCC(=O)OCCCCCCCC RXJJVYBGRFLCOX-UHFFFAOYSA-N 0.000 description 1
- 239000002612 dispersion medium Substances 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000002296 dynamic light scattering Methods 0.000 description 1
- 238000000921 elemental analysis Methods 0.000 description 1
- 239000000598 endocrine disruptor Substances 0.000 description 1
- 231100000049 endocrine disruptor Toxicity 0.000 description 1
- 229920001249 ethyl cellulose Polymers 0.000 description 1
- 235000019325 ethyl cellulose Nutrition 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 238000009499 grossing Methods 0.000 description 1
- 125000000268 heptanoyl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000003104 hexanoyl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000001863 hydroxypropyl cellulose Substances 0.000 description 1
- 235000010977 hydroxypropyl cellulose Nutrition 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- SKHXHUZZFVMERR-UHFFFAOYSA-L isopropyl citrate Chemical compound CC(C)OC(=O)CC(O)(C([O-])=O)CC([O-])=O SKHXHUZZFVMERR-UHFFFAOYSA-L 0.000 description 1
- 235000019300 isopropyl citrate Nutrition 0.000 description 1
- 238000007561 laser diffraction method Methods 0.000 description 1
- 125000000400 lauroyl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000012669 liquid formulation Substances 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 235000011160 magnesium carbonates Nutrition 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- 125000000628 margaroyl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000002609 medium Substances 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 235000019426 modified starch Nutrition 0.000 description 1
- 229920005615 natural polymer Polymers 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- 125000001402 nonanoyl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
- 125000002801 octanoyl group Chemical group C(CCCCCCC)(=O)* 0.000 description 1
- 230000009965 odorless effect Effects 0.000 description 1
- 125000001312 palmitoyl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 238000005375 photometry Methods 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 229920001495 poly(sodium acrylate) polymer Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000011085 pressure filtration Methods 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 230000001953 sensory effect Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical group [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 description 1
- KKCBUQHMOMHUOY-UHFFFAOYSA-N sodium oxide Chemical compound [O-2].[Na+].[Na+] KKCBUQHMOMHUOY-UHFFFAOYSA-N 0.000 description 1
- 229910001948 sodium oxide Inorganic materials 0.000 description 1
- NNMHYFLPFNGQFZ-UHFFFAOYSA-M sodium polyacrylate Chemical compound [Na+].[O-]C(=O)C=C NNMHYFLPFNGQFZ-UHFFFAOYSA-M 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 239000001384 succinic acid Substances 0.000 description 1
- 150000003900 succinic acid esters Chemical class 0.000 description 1
- 230000000475 sunscreen effect Effects 0.000 description 1
- 239000000516 sunscreening agent Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 239000012085 test solution Substances 0.000 description 1
- 238000009210 therapy by ultrasound Methods 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- KENFVQBKAYNBKN-UHFFFAOYSA-N trihexadecyl phosphate Chemical compound CCCCCCCCCCCCCCCCOP(=O)(OCCCCCCCCCCCCCCCC)OCCCCCCCCCCCCCCCC KENFVQBKAYNBKN-UHFFFAOYSA-N 0.000 description 1
- FDGZUBKNYGBWHI-UHFFFAOYSA-N trioctadecyl phosphate Chemical compound CCCCCCCCCCCCCCCCCCOP(=O)(OCCCCCCCCCCCCCCCCCC)OCCCCCCCCCCCCCCCCCC FDGZUBKNYGBWHI-UHFFFAOYSA-N 0.000 description 1
- DUHIKWRPAQIIBL-UHFFFAOYSA-N tris(2-ethylhexyl) 2-hydroxypropane-1,2,3-tricarboxylate Chemical compound CCCCC(CC)COC(=O)CC(O)(C(=O)OCC(CC)CCCC)CC(=O)OCC(CC)CCCC DUHIKWRPAQIIBL-UHFFFAOYSA-N 0.000 description 1
- SVETUDAIEHYIKZ-IUPFWZBJSA-N tris[(z)-octadec-9-enyl] phosphate Chemical compound CCCCCCCC\C=C/CCCCCCCCOP(=O)(OCCCCCCCC\C=C/CCCCCCCC)OCCCCCCCC\C=C/CCCCCCCC SVETUDAIEHYIKZ-IUPFWZBJSA-N 0.000 description 1
- 125000000297 undecanoyl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
Images
Classifications
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- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
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- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
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- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
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- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K13/00—Use of mixtures of ingredients not covered by one single of the preceding main groups, each of these compounds being essential
- C08K13/02—Organic and inorganic ingredients
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/24—Acids; Salts thereof
- C08K3/26—Carbonates; Bicarbonates
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
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- C08K5/10—Esters; Ether-esters
- C08K5/101—Esters; Ether-esters of monocarboxylic acids
- C08K5/103—Esters; Ether-esters of monocarboxylic acids with polyalcohols
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
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- C08K5/11—Esters; Ether-esters of acyclic polycarboxylic acids
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- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
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- A61K2800/10—General cosmetic use
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
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- C08K3/20—Oxides; Hydroxides
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- C08K2003/2217—Oxides; Hydroxides of metals of magnesium
- C08K2003/222—Magnesia, i.e. magnesium oxide
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
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- C08K2003/2224—Magnesium hydroxide
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- C—CHEMISTRY; METALLURGY
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- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K2201/00—Specific properties of additives
- C08K2201/002—Physical properties
- C08K2201/005—Additives being defined by their particle size in general
Definitions
- the present disclosure relates to a cellulose acylate composition and a method for producing the same. Specifically, the present disclosure relates to a cellulose acylate composition used in cosmetic compositions and a method for producing the same.
- cosmetics have been blended with various polymer microparticles for the purpose of improving spreadability, changing the texture, imparting wrinkle blurring effects, and improving the slipperiness of foundations and the like.
- fine particles with a high degree of sphericity are excellent in tactile sensation, and can provide a light scattering (soft focus) effect depending on their physical properties and shape.
- it can be expected to have the effect of smoothing the unevenness of the skin and scattering light in various directions to make wrinkles less noticeable (soft focus).
- Fine particles made of synthetic polymers such as polyamide, polymethyl methacrylate (PMMA), polystyrene, polypropylene, and polyethylene have been used as fine particles to be blended in such cosmetics.
- PMMA polymethyl methacrylate
- polystyrene polystyrene
- polypropylene polyethylene
- polyethylene polyethylene
- US Pat. No. 6,300,000 discloses a process for forming a polysaccharide ester product from polysaccharide synthesis, said polysaccharide ester product comprising a polysaccharide ester and a solvent; diluting said polysaccharide ester product, thereby forming a polysaccharide ester dope. and forming a plurality of polysaccharide ester microspheres from said polysaccharide ester dope, wherein cosmetic compositions are cited as articles that may contain the polysaccharide ester microspheres.
- the volume average particle diameter D50 measured using a laser diffraction particle size distribution analyzer is 72 ⁇ m or more and 100 ⁇ m or less, the degree of polymerization is 131 or more and 350 or less, and the degree of substitution is 2.1 or more and 2 0.6 or less, cellulose acylate is described. Also, a method for producing cellulose acylate comprising an acylation step of acylating cellulose in the presence of sulfuric acid, and a deacylation step of deacylating the acylated cellulose in the presence of acetic acid in a polar solvent. is stated to be preferred.
- a resin component (A) such as a thermoplastic resin and a water-soluble auxiliary agent component (B) are kneaded to prepare a dispersion, and the auxiliary agent component (B) is eluted from the dispersion.
- a molded body for example, a porous body, spherical particles
- a resin component (A) a resin component (A)
- a cellulose derivative such as cellulose acetate
- Patent Document 4 discloses that the average particle diameter is 80 nm or more and 100 ⁇ m or less, the sphericity is 0.7 or more and 1.0 or less, the surface smoothness is 80% or more and 100% or less, and the total degree of acetyl substitution is 0.7 or more.
- Cellulose acetate particles are disclosed that are 2.9 or less.
- the polysaccharide engineered stelmicrospheres of Patent Document 1 are porous particles with a large particle size and a broad particle size distribution, and are not sufficient as a substitute for fine particles of synthetic polymers blended in cosmetics and the like.
- the cellulose acylate obtained by the production method described in Patent Document 2 is also amorphous and porous particles.
- the particulate compact obtained by the manufacturing method described in Patent Document 3 is also particles with a low degree of sphericity and a substantially spherical shape.
- the cellulose acetate particles disclosed in Patent Document 4 are said to have excellent tactile sensation due to their high sphericity and surface smoothness, and to obtain a light scattering (soft focus) effect when blended in a cosmetic composition.
- a cosmetic composition in the field of cosmetic compositions, there is a strong demand for fine particles conforming to standards for quasi-drug raw materials.
- microparticles that do not change over time even during long-term storage and can be formulated into cosmetic compositions in compliance with these standards (particularly pH standards).
- the temporal stability of conventionally known cellulose acetate particles has room for further improvement.
- An object of the present disclosure is to provide a cellulose acylate composition that has improved stability over time and maintains excellent physical properties at the initial stage of production for a long period of time, and a method for producing the same.
- the present inventors found that the pH ( 6.0 to 8.0), and furthermore, it was found that it can be a cause of odor generation.
- the cellulose acylate composition according to the present disclosure includes cellulose acylate particles and metal compound-containing particles.
- the total substitution degree of this cellulose acylate is 0.7 or more and 2.9 or less.
- the metal compound is one or more selected from alkali metal compounds and alkaline earth metal compounds.
- Preferred metal compounds are hydroxides, oxides or carbonates of alkali metals or alkaline earth metals.
- a preferred alkali metal is sodium.
- Preferred alkaline earth metals are calcium or magnesium.
- the average particle size of the metal compound-containing particles is preferably 20 nm or more and 20 ⁇ m or less.
- the metal compound-containing particles are aggregates.
- the cellulose acylate composition contains alkali metals and alkaline earth metals at a total concentration of 50 ppm or more and 2000 ppm or less.
- the average particle size of the cellulose acylate particles is preferably 80 nm or more and 100 ⁇ m or less.
- the sphericity of the cellulose acylate particles is 0.7 or more and 1.0 or less.
- the surface smoothness of the cellulose acylate particles is 80% or more and 100% or less.
- the substituent of cellulose acylate is preferably an acyl group having 2 or more and 20 or less carbon atoms.
- Preferred acyl groups are selected from acetyl, propionyl and butyryl groups.
- the cellulose acylate particles preferably contain a plasticizer.
- the content of this plasticizer is 2% by weight or more and 40% by weight or less with respect to the cellulose acylate particles.
- Preferred plasticizers are one or more selected from the group consisting of citric acid-based plasticizers, glycerin ester-based plasticizers, adipic acid-based plasticizers, and phthalic acid-based plasticizers.
- the cosmetic composition of the present disclosure contains any one of the cellulose acylate compositions described above.
- the method for producing the cellulose acylate composition of the present disclosure comprises (1) A first step of mixing a cellulose acylate having a total substitution degree of 0.7 or more and 2.9 or less and a plasticizer to obtain a cellulose acylate impregnated with a plasticizer (2) Impregnated with a plasticizer a second step of kneading the obtained cellulose acylate and the water-soluble polymer at 200° C. or more and 280° C. or less to obtain a dispersion containing the cellulose acylate impregnated with the plasticizer as a dispersoid; It includes a third step of removing the water-soluble polymer to obtain cellulose acylate particles.
- one or more metal compounds selected from alkali metal compounds and alkaline earth metal compounds are added to the cellulose acylate particles during and/or after the third step. be.
- the metal compound is added by washing the dispersion at least once with a solution containing the metal compound.
- the solution containing the metal compound is an aqueous solution.
- the amount of the metal compound added to 100 parts by weight of the cellulose acylate particles is preferably 0.01 parts by weight or more and 1.0 parts by weight or less.
- the cellulose acylate composition of the present disclosure contains alkali metal compound-containing particles and/or alkaline earth metal compound-containing particles. These metal compound-containing particles suppress elimination of free acid from cellulose acylate. According to this cellulose acylate composition, it is possible to avoid changes over time due to elimination of free acids. This cellulose acylate composition has excellent stability over time. In addition, a cosmetic composition containing this cellulose acylate composition exhibits excellent physical properties in the early stage of production even after a long period of time.
- FIG. 1 is an electron micrograph of the cellulose acylate composition of Example 1.
- FIG. 2 is an electron micrograph of Comparative Example 1.
- FIG. 1 is an electron micrograph of the cellulose acylate composition of Example 1.
- FIG. 2 is an electron micrograph of Comparative Example 1.
- X to Y indicating the range means “X or more and Y or less”. Also, unless otherwise noted, all test temperatures are room temperature (20°C ⁇ 5°C).
- the cellulose acylate composition of the present disclosure contains cellulose acylate particles and metal compound-containing particles.
- the total degree of substitution of cellulose acylate is 0.7 or more and 2.9 or less.
- the metal compound is one or more selected from alkali metal compounds and alkaline earth metal compounds.
- the cellulose acylate composition may contain other metal compounds as unavoidable impurities.
- the main component of the metal compound-containing particles is a metal compound selected from alkali metal compounds and alkaline earth metal compounds.
- the metal compound-containing particles function as a neutralizing agent for the cellulose acylate particles.
- the metal compound-containing particles contribute to suppressing detachment of acetic acid or the like bound to cellulose acylate. Since the cellulose acylate composition avoids a decrease in pH caused by the generation of free acids such as acetic acid, the pH is maintained within the range specified by the standards for raw materials for quasi-drugs, for example, even during long-term storage. , the generation of odors caused by acetic acid and the like is also suppressed. Inclusion of the metal compound-containing particles improves the temporal stability of the cellulose acylate composition.
- the metal compound-containing particles are present substantially independently of the cellulose acylate particles, and are used as additives during the production of the raw material cellulose acylate. It is different from metal compounds that are contained due to impurities and the like. According to the findings of the present inventors, the metal compound-containing particles function as an anti-blocking agent to suppress aggregation of the cellulose acylate particles. Thereby, in the cellulose acylate composition of the present disclosure, in addition to the tactile sensation such as smoothness and moistness, the tactile sensation is also improved in the sense that lumps are less likely to form. When the cellulose acylate composition of the present disclosure is blended into a cosmetic composition, the excellent quality at the time of production can be maintained at a high level for a long period of time.
- metal compounds include compounds of alkali metals such as sodium, lithium, and potassium, or compounds of alkaline earth metals such as calcium, magnesium, and barium.
- Preferred alkali metals are sodium
- preferred alkaline earth metals are calcium and magnesium.
- Examples include hydroxides such as sodium hydroxide, calcium hydroxide and magnesium hydroxide, oxides such as sodium oxide, calcium oxide and magnesium oxide, and carbonates such as sodium carbonate, calcium carbonate and magnesium carbonate. More preferred are calcium carbonate, calcium hydroxide, magnesium carbonate and magnesium hydroxide.
- the metal compound is calcium hydroxide
- the reaction with carbon dioxide in the air may produce calcium carbonate, and such a cellulose acylate composition is also included in the technical scope of the present application.
- the average particle size of the metal compound-containing particles is preferably 20 nm or more and 20 ⁇ m or less. From the viewpoint of ease of production, the average particle size of the metal compound-containing particles is more preferably 50 nm or more, and even more preferably 1 ⁇ m or more. From the viewpoint of improving tactile sensation, the average particle size of the metal compound-containing particles is more preferably 15 ⁇ m or less, and even more preferably 12 ⁇ m or less.
- the average particle size of the metal compound-containing particles is obtained by measuring the major and minor diameters of each particle using an image of the particles observed with a scanning electron microscope (SEM), calculating the average value, and randomly selecting 30 obtained as a numerical average value.
- SEM scanning electron microscope
- the metal compound-containing particles may be aggregates.
- the average particle size of the aggregates is preferably within the above-described numerical range.
- the content of the metal compound-containing particles in the cellulose acylate composition of the present disclosure is not particularly limited, but the total concentration of the alkali metal and alkaline earth metal is preferably 50 ppm or more and 2000 ppm or less.
- a cellulose acylate composition containing a total of 50 ppm or more of alkali metals and alkaline earth metals effectively suppresses a decrease in pH and improves stability over time. If the total concentration of alkali metals and alkaline earth metals exceeds 2000 ppm, the pH may rise outside the desired range during production.
- the metal concentration in the cellulose acylate composition is measured by absorption photometry using an atomic absorption photometer. Details will be described later in Examples.
- the average particle size of the cellulose acylate particles may be 80 nm or more and 100 ⁇ m or less, 100 nm or more, 1 ⁇ m or more, 2 ⁇ m or more, or 4 ⁇ m or more. Also, it may be 80 ⁇ m or less, 40 ⁇ m or less, 20 ⁇ m or less, or 14 ⁇ m or less. If the average particle size is too large, the tactile sensation is poor and the light scattering (soft focus) effect is reduced. On the other hand, if the average particle size is too small, production becomes difficult.
- the tactile sensation includes not only the tactile sensation of direct contact with the cellulose acylate particles, but also the tactile feel and tactile sensation of blending in a cosmetic composition.
- the average particle size can be measured using a dynamic light scattering method. Specifically, it is as follows. First, a sample is prepared by adding cellulose acylate particles to pure water so as to have a concentration of 100 ppm and making a pure water suspension using an ultrasonic vibration device. After that, by the laser diffraction method (Horiba, Ltd.
- the coefficient of variation in particle size of the cellulose acylate particles may be 0% or more and 60% or less, or may be 2% or more and 50% or less.
- the particle size variation coefficient (%) can be calculated by (standard deviation of particle size/average particle size ⁇ 100).
- the sphericity of the cellulose acylate particles is preferably 0.7 or more and 1.0 or less, more preferably 0.8 or more and 1.0 or less, and even more preferably 0.9 or more and 1.0 or less. If the sphericity is less than 0.7, the tactile feel is poor, and for example, even when blended in a cosmetic composition, the tactile feel and soft focus effect are reduced.
- the sphericity can be measured by the following method. Using the image of the particles observed with a scanning electron microscope (SEM), the major axis and minor axis of 30 randomly selected particles are measured, the minor axis/major axis ratio of each particle is obtained, and the minor axis/major axis is obtained. Let the average value of the ratios be the sphericity. It should be noted that the closer the sphericity is to 1, the more sphericity can be determined.
- SEM scanning electron microscope
- the surface smoothness of the cellulose acylate particles is preferably 80% or more and 100% or less, more preferably 85% or more and 100% or less, and even more preferably 90% or more and 100% or less. If the surface smoothness is less than 80%, the feel is poor. The closer it is to 100%, the more favorable the feel is.
- the surface smoothness can be determined based on the area of the recesses by taking a scanning electron micrograph of the particles and observing the unevenness of the particle surface. Details will be described later in Examples.
- the cellulose acylate forming the cellulose acylate particles has a total substitution degree of 0.7 or more and 2.9 or less, preferably 0.7 or more and less than 2.6, more preferably 1.0 or more and less than 2.6, 2.0 or more and less than 2.6 is more preferable. This is because it is easy to produce spherical particles with excellent moldability and high sphericity.
- the total degree of substitution is less than 0.7, the water-solubility is high, and the cellulose acylate is soluble in the process of extracting the particles in the production of the cellulose acylate particles described below, particularly in the process of removing the water-soluble polymer from the dispersion. It is easily eluted, and the sphericity of the resulting particles may decrease, resulting in poor tactile sensation.
- the total degree of substitution of cellulose acylate can be measured by the following method.
- the total degree of substitution of cellulose acylate is the sum of the degrees of substitution at positions 2, 3 and 6 of the glucose ring of cellulose acylate.
- the degree can be measured by the NMR method according to the method of Tezuka (Carbonydr. Res. 273, 83 (1995)). That is, free hydroxyl groups of cellulose acylate are acylated with carboxylic acid anhydride in pyridine.
- the type of carboxylic anhydride used here should be selected according to the purpose of analysis. For example, acetic anhydride is good for analyzing the degree of propionyl substitution of cellulose acetate propionate, and is preferably propionic anhydride.
- the solvent and acid anhydride for the acylation reaction may be appropriately selected according to the cellulose acylate to be analyzed.
- a sample obtained by acylation is dissolved in deuterated chloroform, and the 13 C-NMR spectrum is measured.
- the substituent is an acetyl group, a propionyl group or a butyryl group
- the carbon signal of the acetyl group is in the region of 169 ppm to 171 ppm from the high magnetic field in the order of 2-, 3-, and 6-positions of the propionyl group.
- the carbonyl carbon signals appear in the same order in the region from 172 ppm to 174 ppm
- the butyryl group carbon signals appear in the region from 171 ppm to 173 ppm in the order of 2nd, 3rd and 6th positions from the high magnetic field side.
- the carbonyl of the propionyl group Carbon signals appear in the same order in the region from 172 ppm to 174 ppm.
- the total degree of substitution of cellulose acylate treated with carboxylic anhydride is 3.0. If the sum of the areas of the carbonyl signals of the groups is normalized to 3.0, and the abundance ratio of the acetyl group and the propionyl group at the corresponding positions (the area ratio of each signal) is obtained, the glucose ring in the original cellulose acylate can be obtained. Each degree of acyl substitution at the 2-, 3-, and 6-positions can be determined. Needless to say, substituents containing acyl groups that can be analyzed by this method are only substituents that do not correspond to the carboxylic anhydride used for the treatment for analytical purposes.
- the total degree of substitution at the 2-, 3- and 6-positions of the glucose ring of the sample cellulose acylate is 3.0, and all the substituents are limited substituents such as acetyl and propionyl groups.
- the NMR spectrum can be measured by directly dissolving the sample in deuterated chloroform, excluding the acylation step. If the substituents are all acetyl and propionyl groups, the carbon signals of the acetyl groups are in the region from 169 ppm to 171 ppm in the order 2, 3, 6 from the high magnetic field, as in the case involving the step of acylation.
- the propionyl group carbon signals appear in the same order in the region from 172 ppm to 174 ppm, so from the abundance ratio of the acetyl group and the propionyl group at the corresponding positions (in other words, the area ratio of each signal), the cellulose acylate It is possible to determine the degree of substitution such as the degree of acetyl and propionyl substitution at the 2-, 3-, and 6-positions of the glucose ring in .
- the cellulose acylate forming the cellulose acylate particles of the present disclosure preferably has an acyl group having 2 or more and 20 or less carbon atoms.
- the number of carbon atoms in the acyl group may be 3 or more, or 4 or more. Also, the number of carbon atoms in the acyl group may be 18 or less, or 16 or less.
- Cellulose acylate may have two or more acyl groups with different carbon numbers.
- acyl groups having 2 to 20 carbon atoms include acetyl, propionyl, butyryl, pentanoyl (valeryl), hexanoyl, heptanoyl, octanoyl, nonanoyl, undecanoyl, dodecanoyl, and tridecanoyl groups. , tetradecanoyl (myristoyl) group, pentadecanoyl group, hexadecanoyl group, heptadecanoyl group and octadecanoyl (stearoyl) group.
- One or more acyl groups selected from acetyl, propionyl and butyryl groups are preferred.
- the cellulose acylate particles may or may not contain a plasticizer.
- a plasticizer in the present disclosure refers to a compound capable of increasing the plasticity of cellulose acylate.
- the plasticizer is not particularly limited, and examples thereof include dimethyl adipate, dibutyl adipate, diisostearyl adipate, diisodecyl adipate, diisononyl adipate, diisobutyl adipate, diisopropyl adipate, and diethylhexyl adipate.
- Adipate plasticizers including adipates such as dioctyl, dioctyldodecyl adipate, dicapryl adipate and dihexyldecyl adipate; acetyltriethyl citrate, acetyltributyl citrate, isodecyl citrate, isopropyl citrate, triethyl citrate, Citric acid-based plasticizers, including citrate esters such as triethylhexyl citrate and tributyl citrate; glutaric acid-based plasticizers, including glutarate esters such as diisobutyl glutarate, dioctyl glutarate and dimethyl glutarate; succinic acid plasticizers, including succinic acid esters such as diethyl acid, diethylhexyl succinate and dioctyl succinate; Sebacic acid plasticizers, including sebacate esters; glycerin ester
- citric acid plasticizers including citric acid esters such as triethyl citrate, acetyltriethyl citrate and acetyltributyl citrate; glycerol ester plasticizers, including glycerol alkyl esters such as triacetin, diacetin and monoacetin; and adipine.
- citric acid plasticizers including citric acid esters such as triethyl citrate, acetyltriethyl citrate and acetyltributyl citrate
- glycerol ester plasticizers including glycerol alkyl esters such as triacetin, diacetin and monoacetin
- adipine One or more selected from the group consisting of adipic acid-based plasticizers such as diisononyl acid is preferred, and selected from the group consisting of triethyl citrate, acetyltriethyl citrate, acetyltributy
- phthalic acid-based plasticizers can be used, they should be used with caution due to concerns about their similarity to endocrine disruptors.
- the content of the plasticizer contained in the cellulose acylate particles is not particularly limited. For example, it may be more than 0% by weight and 40% by weight or less, may be 2% by weight or more and 40% by weight or less, or may be 10% by weight or more and 30% by weight or less, relative to the weight of the cellulose acylate particles. , 15% by weight or more and 20% by weight or less.
- the content of the plasticizer in the cellulose acylate particles is determined by dissolving the cellulose acylate particles in a solvent capable of dissolving the cellulose acylate particles and measuring the solution by 1 H-NMR.
- the cellulose acylate composition of the present disclosure can be produced by the below-described production method.
- the cellulose acylate composition of the present disclosure has high stability over time and excellent tactile sensation, and thus can be suitably used in cosmetic compositions.
- due to its high sphericity when blended in a cosmetic composition, it has the effect of filling uneven skin to make it smooth and scattering light in various directions to make wrinkles less noticeable (soft focus). can get.
- the cellulose acylate composition of the present disclosure such excellent physical properties immediately after production can be maintained for a long period of time.
- Cosmetic compositions include foundations such as liquid foundations and powder foundations; concealers; sunscreens; makeup bases; rouge and lipstick bases; and skin and hair external preparations mainly for cosmetic purposes, such as skin care lotions, and the dosage form is not limited.
- the dosage form may be any of liquid formulations such as aqueous solutions, emulsions and suspensions; semi-solid formulations such as gels and creams; and solid formulations such as powders, granules and solid formulations. Further, it may be an emulsion type such as cream or milky lotion; an oil gel type such as lipstick; a powder type such as foundation; or an artificial asol type such as hair styling agent.
- a cellulose acylate having a total substitution degree of 0.7 or more and 2.9 or less and a plasticizer are mixed to obtain a cellulose acylate impregnated with a plasticizer.
- the cellulose acylate impregnated with the plasticizer and the water-soluble polymer are kneaded at 200° C. or more and 280° C. or less to obtain a dispersion containing the cellulose acylate impregnated with the plasticizer as a dispersoid.
- a third step of removing the water-soluble polymer from this dispersion to obtain cellulose acylate particles By adding one or more metal compounds selected from alkali metal compounds and alkaline earth metal compounds to the cellulose acylate particles during and/or after the third step, the present A disclosed cellulose acylate composition is produced.
- a cellulose acylate having a total substitution degree of 0.7 or more and 2.9 or less can be produced by a known production method.
- a pretreatment step of sprinkling and mixing the raw material pulp with acetic acid after disintegration and crushing may be included.
- post-treatment steps of sedimentation, purification, stabilization and drying may be included.
- the total degree of substitution of cellulose acylate can be adjusted by adjusting the conditions of the aging process (conditions such as time and temperature).
- the type of substituent can be made by selecting the esterifying agent.
- the total degree of substitution of the obtained cellulose acylate is 0.7 or more and 2.9 or less, preferably 0.7 or more and less than 2.6, more preferably 1.0 or more and less than 2.6, and 1.4 or more. Less than 2.6 is more preferable, and 2.0 or more and less than 2.6 is particularly preferable.
- any one having a plasticizing effect in melt extrusion processing of cellulose acylate can be used without any particular limitation. can be used alone or in combination of two or more.
- One or more selected from the group consisting of citric acid-based plasticizers, glycerol ester-based plasticizers, adipic acid-based plasticizers and phthalic acid-based plasticizers are preferred, and acetyltriethyl citrate, triacetin, diacetin and phthalic acid. More preferably, one or more selected from the group consisting of jetyl.
- the blending amount of the plasticizer may be more than 0 parts by weight and 40 parts by weight or less, or may be 2 parts by weight or more and 40 parts by weight or less, with respect to 100 parts by weight as the total amount of the cellulose acylate and the plasticizer. It may be 10 parts by weight or more and 30 parts by weight or less, or may be 15 parts by weight or more and 20 parts by weight or less. If the amount is too small, the sphericity of the obtained cellulose acylate particles tends to decrease, and if it is too large, the shape of the particles cannot be maintained and the sphericity tends to decrease.
- the cellulose acylate and plasticizer can be mixed dry or wet using a mixer such as a Henschel mixer.
- a mixer such as a Henschel mixer
- the temperature in the mixer may be set to a temperature at which cellulose acylate does not melt, for example, in the range of 20°C or higher and lower than 200°C.
- the cellulose acylate and plasticizer may be mixed by melt-kneading. Melt-kneading may be combined with mixing using a mixer such as a Henschel mixer. In that case, the mixture may be mixed at a temperature of 20°C or higher and lower than 200°C using a mixer such as a Henschel mixer, and then melt-kneaded. preferable. Since the plasticizer and the cellulose acylate are more uniformly compatible with each other in a short period of time, the sphericity of the obtained cellulose acylate particles is increased, and the tactile sensation and tactile sensation are improved.
- Melt-kneading can be performed by heating and mixing with an extruder.
- the kneading temperature (cylinder temperature) of the extruder may be 200°C to 230°C.
- a uniform kneaded product can be obtained by plasticizing even at a temperature within this range. If the temperature is too low, the sphericity of the resulting particles will be low, resulting in poor tactile sensation and feel. In addition, there is a possibility that the viscosity of the melt will decrease and kneading of the resin in the extruder will be insufficient.
- the melting point of cellulose acylate is about 230° C. to 280° C., although it depends on the type and degree of substitution of the substituents, which is close to the decomposition temperature of cellulose acylate, so melt-kneading in this temperature range is usually difficult.
- cellulose acylate (flakes) impregnated with a plasticizer can lower the plasticizing temperature.
- the kneading temperature (cylinder temperature) may be 200° C. when using a twin-screw extruder, for example.
- the kneaded product may be extruded in the form of strands and cut into pellets by hot cutting or the like.
- the die temperature in this case may be about 220.degree.
- the cellulose acylate impregnated with the plasticizer and the water-soluble polymer are kneaded at 200° C. or higher and 280° C. or lower to obtain a dispersion containing the cellulose acylate as a dispersoid.
- the cellulose acylate impregnated with the plasticizer and the water-soluble polymer can be kneaded with an extruder such as a twin-screw extruder.
- the kneading temperature refers to the cylinder temperature.
- the dispersion may be extruded in a string shape from a die attached to the tip of an extruder such as a twin-screw extruder, and then cut into pellets.
- the die temperature may be 220° C. or more and 300° C. or less.
- the blending amount of the water-soluble polymer may be 55 parts by weight or more and 99 parts by weight or less with respect to 100 parts by weight as the total amount of the cellulose acylate impregnated with the plasticizer and the water-soluble polymer. It is preferably 60 to 90 parts by weight, more preferably 65 to 85 parts by weight.
- a water-soluble polymer refers to a polymer having an insoluble content of less than 50% by weight when 1 g of the polymer is dissolved in 100 g of water at 25°C.
- water-soluble polymers include polyvinyl alcohol, polyethylene glycol, sodium polyacrylate, polyvinylpyrrolidone, polypropylene oxide, polyglycerin, polyethylene oxide, vinyl acetate, modified starch, thermoplastic starch, methyl cellulose, ethyl cellulose, hydroxyl Ethyl cellulose, hydroxypropyl cellulose and the like can be mentioned.
- polyvinyl alcohol, polyethylene glycol and thermoplastic starch are preferred, and polyvinyl alcohol and thermoplastic starch are particularly preferred.
- Thermoplastic starch can be obtained by a known method.
- Japanese Patent Publication No. 6-6307, WO92/04408, etc. can be referred to, and more specifically, for example, tapioca starch is mixed with about 20% glycerin as a plasticizer and kneaded with a twin-screw extruder. is available.
- the dispersion obtained in the second step is a dispersion containing a water-soluble polymer as a dispersion medium and a cellulose acylate impregnated with a plasticizer as a dispersoid.
- the water-soluble polymer is the sea component
- the cellulose acylate impregnated with the plasticizer is the island component.
- the kneaded material constituting the island component contains cellulose acylate and a plasticizer and is mainly spherical.
- the method for removing the water-soluble polymer is not particularly limited as long as the water-soluble polymer can be dissolved and removed from the particles.
- Examples thereof include a method of dissolving and removing the water-soluble polymer in the dispersion using a solvent such as water; an alcohol such as methanol, ethanol or isopropanol; or a mixed solution thereof.
- a solvent such as water
- an alcohol such as methanol, ethanol or isopropanol
- a mixed solution thereof for example, after mixing the dispersion and the solvent, the solvent in which the water-soluble polymer is dissolved is separated by solid-liquid separation such as filtration, thereby removing the water-soluble polymer from the dispersion. method.
- the stirring and mixing and filtering may be repeated multiple times for the purpose of increasing the removal efficiency.
- the plasticizer may or may not be removed from the dispersion together with the water-soluble polymer. Therefore, the cellulose acylate particles obtained may or may not contain a plasticizer.
- the mixing ratio of the dispersion and the solvent may be 0.01 wt% or more and 20 wt% or less, or 2 wt% or more and 15 wt% or less of the total weight of the dispersion and the solvent. It may be 4% by weight or more and 13% by weight or less. If the content of the dispersion exceeds 20% by weight, the dissolution of the water-soluble polymer may be insufficient and it may not be possible to remove it by washing. In addition, it becomes difficult to separate the cellulose acylate particles not dissolved in the solvent from the solvent in which the water-soluble polymer is dissolved by an operation such as filtration or centrifugation.
- the temperature for mixing the dispersion and the solvent is preferably 0°C or higher and 200°C or lower, more preferably 20°C or higher and 110°C or lower, and even more preferably 40°C or higher and 80°C or lower.
- the temperature is lower than 0°C, the solubility of the water-soluble polymer becomes insufficient and it becomes difficult to remove it by washing. It becomes difficult to take out the particles.
- the mixing time of the dispersion and the solvent is not particularly limited and may be adjusted as appropriate. can be
- the method of mixing the dispersion and the solvent is not particularly limited as long as the water-soluble polymer can be dissolved and removed.
- a water-soluble polymer can be removed from the dispersion.
- the number of revolutions during mixing of the dispersion and the solvent may be, for example, 5 rpm or more and 3000 rpm or less.
- the water-soluble polymer can be removed from the dispersion more efficiently. It also effectively removes the plasticizer from the dispersion.
- one or more metal compounds selected from alkali metal compounds and alkaline earth metal compounds are added during and/or after the third step. is added to the cellulose acylate particles.
- the cellulose acylate composition of the present disclosure which contains the metal compound-containing particles that act as a neutralizing agent and an antiblocking agent, can be obtained.
- the compounds described above as the metal compound contained in the cellulose acylate composition can be used singly or in combination of two or more.
- Alkali metal or alkaline earth metal hydroxides, oxides or carbonates are preferred, with calcium carbonate, calcium hydroxide, magnesium carbonate and magnesium hydroxide being more preferred.
- the amount of metal compound added is preferably 0.01 parts by weight or more and 1.0 parts by weight or less with respect to 100 parts by weight of cellulose acylate. From the viewpoint of stability over time and improvement of touch feeling, the amount of the metal compound added may be 0.02 parts by weight or more, and may be 0.05 parts by weight or more. From the viewpoint that the pH satisfies the standard, the amount of the metal compound added may be 0.8 parts by weight or less, and may be 0.06 parts by weight or less.
- a method of adding a metal compound after the third step for example, a method of adding a metal compound to the cellulose acylate particles obtained in the third step and mixing with a mixer such as a ball mill can be mentioned.
- the metal compound may be added in the form of powder or particles, and may be added as a solution or suspension.
- a method of adding the metal compound during the third step for example, a method of adding the metal compound to the solvent for removing the water-soluble polymer, or a method of using a solution containing the metal compound instead of the solvent. mentioned.
- the dispersion is washed with a solution containing the metal compound to remove the water-soluble polymer and add the metal compound.
- the solution containing the metal compound is preferably an aqueous solution.
- a cellulose acylate composition containing metal compound-containing particles with a smaller particle size can be obtained than when the metal compound is added after the third step. This remarkably improves the texture of the resulting cellulose acylate composition. Therefore, the method of adding the metal compound during the third step is more preferable.
- a Henschel mixer manufactured by Nippon Coke Kogyo Co., Ltd.
- the obtained mixture was supplied to a twin-screw extruder (PCM30 manufactured by Ikegai Co., Ltd., cylinder temperature: 200°C, die temperature: 220°C), melt-kneaded, extruded and pelletized to obtain a kneaded product.
- PCM30 manufactured by Ikegai Co., Ltd., cylinder temperature: 200°C, die temperature: 220°C
- Calcium hydroxide (manufactured by Fujifilm Wako Pure Chemical Industries, Ltd.) was dissolved in pure water to prepare a calcium hydroxide aqueous solution with a concentration of 1000 ppm. This calcium hydroxide aqueous solution and pure water were added to the filter cake taken out.
- the amounts of pure water and calcium hydroxide aqueous solution added were respectively 600 parts by weight and 15 parts by weight (0.015% by weight as calcium hydroxide) with respect to 100 parts by weight of cellulose diacetate.
- the filter cake to which pure water and an aqueous calcium hydroxide solution have been added is further put into a three-one motor, stirred at a temperature of 80° C. and a rotation speed of 200 rpm for 30 minutes, and then filtered to obtain the cellulose acylate composition of Example 1. got stuff
- Example 1 The obtained cellulose acylate composition of Example 1 was observed with an electron microscope to obtain the image in FIG.
- reference numeral 1 denotes cellulose acylate particles
- reference numeral 2 denotes metal compound-containing particles. From FIG. 1, it was confirmed that the metal compound-containing particles were aggregates and existed separately from the cellulose acylate particles. Elemental analysis using an energy dispersive X-ray spectroscope (EDS) revealed that the main component of the metal compound-containing particles was calcium carbonate.
- EDS energy dispersive X-ray spectroscope
- Examples 2-5, 8 and 10 Cellulose acylate compositions of Examples 2-5, 8 and 10 were prepared in the same manner as in Example 1 except that the types and amounts of additives added to the filter cake were as shown in Tables 1 and 2 below. Obtained.
- a cellulose acylate composition of Example 6 was obtained in the same manner as above.
- Example 9 To the cellulose acylate particles of Comparative Example 1, calcium carbonate (manufactured by Fujifilm Wako Pure Chemical Industries, Ltd.: particle diameter 1 to 3 ⁇ m, average particle diameter 2 ⁇ m) was added in an amount of 100 ppm, and the mixture was placed in a ball mill (manufactured by AS ONE). Then, the cellulose acylate composition of Example 9 was prepared by rotating the cellulose acylate particles and calcium carbonate for 3 hours on a pot mill rotary table (manufactured by Nitto Kagaku Kogyo Co., Ltd.: AN-3S) to homogenize the cellulose acylate particles and calcium carbonate. got
- Metal concentration in each example and comparative example was measured by absorptiometry. Specifically, 3.0 g of a sample was placed in a crucible, carbonized on an electric heater, then placed in an electric furnace and incinerated at 750 to 850° C. for about 2 hours. After the crucible was covered and allowed to cool, 25 ml of a 0.07% hydrochloric acid solution was added and dissolved by heating on a hot plate. After standing to cool, the solution in the crucible was put into a Nalgel flask with a volume of 200 ml. After washing the crucible with distilled water, the washing liquid was also put into the Nalgel flask and diluted with distilled water to the marked line. Using this as a test solution, the absorbance was measured using an atomic absorption photometer to determine the metal concentration (ppm) in the sample.
- Each of the examples and comparative examples was adjusted to a concentration of about 100 ppm using pure water, and made into a suspension using an ultrasonic vibrator. After that, the volume The frequency particle size distribution was determined and the average particle size was measured. The average particle size (nm and ⁇ m) was the particle size value (volume-based median diameter) corresponding to 50% of the cumulative scattering intensity in the volume frequency particle size distribution. .
- compositions of Examples are rated higher than the compositions of Comparative Examples. Moreover, by blending the compositions of the examples, it is possible to obtain a cosmetic composition having excellent tactile sensation. From these evaluation results, the superiority of the present disclosure is clear.
- the cellulose acylate composition described above can be applied to the production of various cosmetic compositions.
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Abstract
Description
(1)総置換度が0.7以上2.9以下のセルロースアシレートと、可塑剤とを混合して、可塑剤が含浸したセルロースアシレートを得る第一の工程
(2)可塑剤が含浸したセルロースアシレートと水溶性高分子とを200℃以上280℃以下で混練して、可塑剤が含浸したセルロースアシレートを分散質とする分散体を得る第二の工程
及び
(3)分散体から水溶性高分子を除去してセルロースアシレート粒子を得る第三の工程
を含んでいる。この製造方法は、第三の工程中及び/又は第三の工程後に、アルカリ金属化合物及びアルカリ土類金属化合物から選択される1種また2種以上の金属化合物が、セルロースアシレート粒子に添加される。
本開示のセルロースアシレート組成物は、セルロースアシレート粒子と、金属化合物含有粒子と、を含む。セルロースアシレートの総置換度は0.7以上2.9以下である。金属化合物は、アルカリ金属化合物及びアルカリ土類金属化合物から選択される1種又は2種以上である。セルロースアシレート組成物が、不可避的不純物として他の金属化合物を含んでもよい。
本開示のセルロースアシレート組成物において、金属化合物含有粒子の主成分は、アルカリ金属化合物及びアルカリ土類金属化合物から選択される金属化合物である。この金属化合物含有粒子は、セルロースアシレート粒子に対し、中和剤として機能する。この金属化合物含有粒子は、セルロースアシレートに結合している酢酸等の脱離抑制に寄与する。このセルロースアシレート組成物では、酢酸等遊離酸の発生に起因するpHの低下が回避されるので、例えば、長期保存中も、医薬部外品原料規格に定められたpHの範囲内に維持され、酢酸等に起因する臭気の発生も抑制される。この金属化合物含有粒子を含むことにより、セルロースアシレート組成物の経時安定性が向上する。
セルロースアシレート粒子の平均粒子径は、80nm以上100μm以下であってよく、100nm以上であってよく、1μm以上であってよく、2μm以上であってよく、4μm以上であってよい。また、80μm以下であってよく、40μm以下であってよく、20μm以下であってよく、14μm以下であってよい。平均粒子径が大きすぎると、その触感に劣る他、光散乱(ソフトフォーカス)効果が低減する。また、平均粒子径が小さすぎると、製造が困難となる。なお、触感としては、セルロースアシレート粒子に直接触れる場合の他、例えば、化粧品組成物に配合した場合の肌触りや触感が挙げられる。
本開示のセルロースアシレート組成物の製造方法は、総置換度が0.7以上2.9以下のセルロースアシレートと可塑剤とを混合して、可塑剤が含浸したセルロースアシレートを得る第一の工程、この可塑剤が含浸したセルロースアシレートと水溶性高分子とを200℃以上280℃以下で混練して、可塑剤が含浸したセルロースアシレートを分散質とする分散体を得る第二の工程、及びこの分散体から水溶性高分子を除去してセルロースアシレート粒子を得る第三の工程を含む。この第三の工程中及び/又は第三の工程後に、アルカリ金属化合物及びアルカリ土類金属化合物から選択される1種また2種以上の金属化合物を、セルロースアシレート粒子に添加することにより、本開示のセルロースアシレート組成物が製造される。
可塑剤が含浸したセルロースアシレートを得る第一の工程においては、総置換度が0.7以上2.9以下のセルロースアシレートと可塑剤とを混合する。
第二の工程においては、可塑剤が含浸したセルロースアシレートと水溶性高分子とを200℃以上280℃以下で混練して、セルロースアシレートを分散質とする分散体を得る。
セルロースアシレート粒子を得る第三の工程では、前述の分散体から水溶性高分子を除去する。
セルロースジアセテート(株式会社ダイセル製:総置換度=2.4)100重量部と、可塑剤としてトリアセチン(株式会社ダイセル製)22重量部とを乾燥状態でプレンドして、80℃で12時間以上乾燥させた後、さらに、ヘンシェルミキサー(日本コークス工業社製)を用いて攪拌混合して、セルロ-スアセテートと可塑剤との混合物を得た。得られた混合物を、二軸押出機(株式会社池貝製PCM30、シリンダー温度:200℃、ダイス温度:220℃)に供給し、溶融混練し、押し出してペレット化し、混練物とした。
ろ物に添加する添加剤の種類及び量を、下表1及び2に示されるものとした以外は、実施例1と同様にして実施例2-5、8及び10のセルロースアシレート組成物を得た。
セルロースジアセテートに代えて、セルロースアセテートプロピオネート(イーストマンケミカル製:CAP-482-0.5、アセチル置換度=0.18、プロピオニル置換度=2.40)を使用した以外は実施例1と同様にして、実施例6のセルロースアシレート組成物を得た。
セルロースジアセテートに代えて、セルロースアセテートブチレート(イーストマンケミカル製:CAB-171-15、アセチル置換度=2.40、ブチリル置換度=0.71)を使用した以外は実施例1と同様にして、実施例7のセルロースアシレート組成物を得た。
ろ物に水酸化カルシウム水溶液を添加せず、純水と合わせて、スリーワンモータを用いて、温度80℃、回転数200rpmで5時間攪拌後、ろ別する作業を3回繰り返すことにより、比較例1のセルロースアシレート粒子を得た。
比較例1のセルロースアシレート粒子に対し、100ppmとなる量で炭酸カルシウム(富士フイルム和光純薬社製:粒子径1~3μm、平均粒子径2μm)を添加して、ボールミル(アズワン社製)に投入し、ポットミル回転台(日陶化学工業社製:AN-3S)にて3時間回転させて、セルロースアシレート粒子と炭酸カルシウムとを均一化させることにより、実施例9のセルロースアシレート組成物を得た。
得られた実施例及び比較例について、下記の方法により、金属濃度、平均粒子径、真球度及び表面平滑度を測定し、触感、製造直後のpH並びに保存後のpH及び臭気を評価した。得られた結果が表1及び2に示されている。
各実施例及び比較例中の金属濃度を、吸光光度法により測定した。具体的には、試料3.0gをルツボに採取して、電熱器上で炭化した後、電気炉に入れて750~850℃で約2時間灰化した。ルツボに蓋をして放冷した後、0.07%塩酸溶液25mlを添加して、ホットプレート上で加温溶解した。放冷後、ルツボ中の溶液を、容積200mlのナルゲルフラスコに投入した。蒸留水でルツボを洗浄した後、洗浄液もナルゲルフラスコに投入し、蒸留水で標線までメスアップした。これを検液として、原子吸光光度計を用いて吸光度を測定して、試料中の金属濃度(ppm)を求めた。
各実施例及び比較例のそれぞれについて、純水を用いて100ppm程度の濃度に調整し、超音波振動装置を用いて懸濁液とした。その後、レーザー回折法(株式会社堀場製作所「レーザー回折/散乱式粒子径分布測定装置LA-960」超音波処理15分、屈折率(1.500、媒体(水;1.333))により、体積頻度粒度分布を求め、平均粒子径を測定した。平均粒子径(nm及びμm)は、体積頻度粒度分布における散乱強度の積算50%に対応する粒子径の値(体積基準のメジアン径)とした。
走査型電子顕微鏡(SEM)で観察したセルロースアシレート粒子の画像を用いて、ランダムに選択した30個の粒子の長径と短径を測定し、各粒子の短径/長径比を求め、その短径/長径比の平均値を真球度とした。
各実施例及び比較例のセルロースアシレート粒子の2500~5000倍の走査型電子顕微鏡写真を撮影した。得られた撮影画像を、画像処理装置Winroof(三谷商事社製))を用いて二値化した。二値化した画像から、粒子1個の中心及び/又は中心付近を含む領域を無作為に選択して、当該領域における凹凸の凹に当たる部分(陰の部分)の面積率を算出し、以下の式によりその粒子1個の表面平滑度(%)を算出した。
粒子1個の表面平滑度(%)=(1-凹の面積率)×100
凹の面積率=前記任意の領域における凹部の面積/前記任意の領域の面積
ランダムに選択した10個の粒子サンプル(n1~n10)の表面平滑度の平均値を、表面平滑度(%)とした。この数値が高いほど、粒子の表面平滑度は高い。なお、面積率の算出に用いる領域は、粒子1個の中心及び/又は中心付近を含む、粒子よりも小さい任意の領域であってよい。その領域の大きさは、粒子径が15μmのとき5μm四方であってよい。
各実施例及び比較例の触感について、20人のパネルテストによる官能評価をおこなった。各組成物に触れさせて、なめらかさ及びしっとり感の両方を総合的に5点満点として評価させた。20人の平均点を算出して、以下の基準により触感を評価した。
良い:A、やや良い:B、普通:C、やや悪い:D、悪い:E
各実施例及び比較例の製造直後のpHと、60℃の恒温槽中で90日間保存した後のpH(経時pH)を、pH計(ガラス電極法)により測定した。具体的には、容量100mlのコニカルビーカーに、50mlの蒸留水を量りとり、スターラーで撹拌しながら、試料2.0gを投入した。30分間撹拌後、加圧ろ過をおこなってろ液を採取した。このろ液をpH計で測定した。
各実施例及び比較例の組成物を60℃の恒温槽中で90日間保存した後、試料1.5gを薬さじで取り出して臭いをかぎ、6段階臭気強度表示法に準じて、次の基準で評価した。
0:無臭
1:やっと感知できる臭い(検知閾値濃度)
2:何の臭いであるかがわかる弱い臭い(認知閾値濃度)
3:らくに感知できる臭い
4:強い臭い
5:強烈な臭い
2・・・金属化合物含有粒子
Claims (18)
- セルロースアシレート粒子と、金属化合物含有粒子と、を含み、
前記セルロースアシレートの総置換度が0.7以上2.9以下であり、
前記金属化合物が、アルカリ金属化合物及びアルカリ土類金属化合物から選択される1種又は2種以上である、セルロースアシレート組成物。 - 前記金属化合物が、アルカリ金属又はアルカリ土類金属の、水酸化物、酸化物又は炭酸塩である、請求項1に記載のセルロースアシレート組成物。
- 前記アルカリ金属がナトリウムであり、前記アルカリ土類金属がカルシウム又はマグネシウムである、請求項2に記載のセルロースアシレート組成物。
- 前記金属化合物含有粒子の平均粒子径が20nm以上20μm以下である、請求項1から3のいずれかに記載のセルロースアシレート組成物。
- 前記金属化合物含有粒子が凝集体である、請求項1から4のいずれかに記載のセルロースアシレート組成物。
- 前記アルカリ金属及びアルカリ土類金属が、合計で50ppm以上2000ppm以下の濃度で含まれている、請求項2から5のいずれかに記載のセルロースアシレート組成物。
- 前記セルロースアシレート粒子の平均粒子径が80nm以上100μm以下である、請求項1から6のいずれかに記載のセルロースアシレート組成物。
- 前記セルロースアシレート粒子の真球度が0.7以上1.0以下である、請求項1から7のいずれかに記載のセルロースアシレート組成物。
- 前記セルロースアシレート粒子の表面平滑度が80%以上100%以下である、請求項1から3のいずれかに記載のセルロースアシレート組成物。
- 前記セルロースアシレートの置換基が、炭素数2以上20以下のアシル基である、請求項1から9のいずれかに記載のセルロースアシレート組成物。
- 前記アシル基が、アセチル基、プロピオニル基及びブチリル基から選択される、請求項10に記載のセルロースアシレート組成物。
- 前記セルロースアシレート粒子が可塑剤を含有しており、
前記可塑剤の含有量が、前記セルロースアシレート粒子に対して2重量%以上40重量%以下である、請求項1から11のいずれかに記載のセルロースアシレート組成物。 - 前記可塑剤が、クエン酸系可塑剤、グリセリンエステル系可塑剤、アジピン酸系可塑剤及びフタル酸系可塑剤からなる群より選択される1種又は2種以上である、請求項12に記載のセルロースアシレート組成物。
- 請求項1から13のいずれかに記載のセルロースアシレート組成物を含有する、化粧品組成物。
- 総置換度が0.7以上2.9以下のセルロースアシレートと、可塑剤とを混合して、前記可塑剤が含浸したセルロースアシレートを得る第一の工程と、
前記可塑剤が含浸したセルロースアシレートと水溶性高分子とを200℃以上280℃以下で混練して、前記可塑剤が含浸したセルロースアシレートを分散質とする分散体を得る第二の工程と、
前記分散体から前記水溶性高分子を除去してセルロースアシレート粒子を得る第三の工程と、を含み、
前記第三の工程中及び/又は第三の工程後に、アルカリ金属化合物及びアルカリ土類金属化合物から選択される1種また2種以上の金属化合物を添加する、セルロースアシレート組成物の製造方法。 - 前記第三の工程中、前記金属化合物を含む溶液で、少なくとも1回、前記分散体を洗浄することにより、前記金属化合物を添加する、請求項15に記載の製造方法。
- 前記金属化合物を含む溶液が水溶液である、請求項15又は16に記載の製造方法。
- 100重量部の前記セルロースアシレートに対する前記金属化合物の添加量が、0.01重量部以上1.0重量部以下である、請求項15から17のいずれかに記載の製造方法。
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KR20230146621A (ko) | 2023-10-19 |
CN116917400A (zh) | 2023-10-20 |
US20240132696A1 (en) | 2024-04-25 |
TW202233735A (zh) | 2022-09-01 |
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US20240228741A9 (en) | 2024-07-11 |
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