JP5150051B2 - 表面変性され、熱分解により製造された二酸化チタン - Google Patents
表面変性され、熱分解により製造された二酸化チタン Download PDFInfo
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- JP5150051B2 JP5150051B2 JP2005372186A JP2005372186A JP5150051B2 JP 5150051 B2 JP5150051 B2 JP 5150051B2 JP 2005372186 A JP2005372186 A JP 2005372186A JP 2005372186 A JP2005372186 A JP 2005372186A JP 5150051 B2 JP5150051 B2 JP 5150051B2
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- alkyl
- aryl
- titanium dioxide
- chf
- coo
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- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 title claims abstract description 103
- 239000004408 titanium dioxide Substances 0.000 title claims abstract description 50
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 86
- 239000000203 mixture Substances 0.000 claims abstract description 45
- 239000000377 silicon dioxide Substances 0.000 claims abstract description 38
- 235000012239 silicon dioxide Nutrition 0.000 claims abstract description 37
- 238000009472 formulation Methods 0.000 claims abstract description 27
- 125000000217 alkyl group Chemical group 0.000 claims description 62
- -1 halo organosilane Chemical class 0.000 claims description 45
- 125000003118 aryl group Chemical group 0.000 claims description 27
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- 238000000034 method Methods 0.000 claims description 14
- 238000000197 pyrolysis Methods 0.000 claims description 14
- 229920002545 silicone oil Polymers 0.000 claims description 12
- 150000001282 organosilanes Chemical class 0.000 claims description 10
- 230000007062 hydrolysis Effects 0.000 claims description 9
- 238000006460 hydrolysis reaction Methods 0.000 claims description 9
- 125000004122 cyclic group Chemical group 0.000 claims description 8
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 8
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- SZVJSHCCFOBDDC-UHFFFAOYSA-N iron(II,III) oxide Inorganic materials O=[Fe]O[Fe]O[Fe]=O SZVJSHCCFOBDDC-UHFFFAOYSA-N 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 229940078546 isoeicosane Drugs 0.000 description 1
- 229930013032 isoflavonoid Natural products 0.000 description 1
- 150000003817 isoflavonoid derivatives Chemical class 0.000 description 1
- 235000012891 isoflavonoids Nutrition 0.000 description 1
- 229940100554 isononyl isononanoate Drugs 0.000 description 1
- KUVMKLCGXIYSNH-UHFFFAOYSA-N isopentadecane Natural products CCCCCCCCCCCCC(C)C KUVMKLCGXIYSNH-UHFFFAOYSA-N 0.000 description 1
- XUGNVMKQXJXZCD-UHFFFAOYSA-N isopropyl palmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC(C)C XUGNVMKQXJXZCD-UHFFFAOYSA-N 0.000 description 1
- 229940089456 isopropyl stearate Drugs 0.000 description 1
- 230000007803 itching Effects 0.000 description 1
- 238000005304 joining Methods 0.000 description 1
- 229940119170 jojoba wax Drugs 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 229940070765 laurate Drugs 0.000 description 1
- 229940061515 laureth-4 Drugs 0.000 description 1
- 229940062711 laureth-9 Drugs 0.000 description 1
- 235000019136 lipoic acid Nutrition 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 239000006210 lotion Substances 0.000 description 1
- 150000002736 metal compounds Chemical class 0.000 description 1
- 229960002216 methylparaben Drugs 0.000 description 1
- MJVGBKJNTFCUJM-UHFFFAOYSA-N mexenone Chemical group OC1=CC(OC)=CC=C1C(=O)C1=CC=C(C)C=C1 MJVGBKJNTFCUJM-UHFFFAOYSA-N 0.000 description 1
- 239000004200 microcrystalline wax Substances 0.000 description 1
- 235000019808 microcrystalline wax Nutrition 0.000 description 1
- 235000013336 milk Nutrition 0.000 description 1
- 210000004080 milk Anatomy 0.000 description 1
- 230000001333 moisturizer Effects 0.000 description 1
- 230000003020 moisturizing effect Effects 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 235000011929 mousse Nutrition 0.000 description 1
- 235000020638 mussel Nutrition 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- JXTPJDDICSTXJX-UHFFFAOYSA-N n-Triacontane Natural products CCCCCCCCCCCCCCCCCCCCCCCCCCCCCC JXTPJDDICSTXJX-UHFFFAOYSA-N 0.000 description 1
- 238000005121 nitriding Methods 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- 239000010466 nut oil Substances 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-M octadecanoate Polymers CCCCCCCCCCCCCCCCCC([O-])=O QIQXTHQIDYTFRH-UHFFFAOYSA-M 0.000 description 1
- ORPJZHOKKGOIGN-KNRYUCGFSA-N octadecanoic acid (2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanal Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C=O.CCCCCCCCCCCCCCCCCC(O)=O.CCCCCCCCCCCCCCCCCC(O)=O ORPJZHOKKGOIGN-KNRYUCGFSA-N 0.000 description 1
- CKQVRZJOMJRTOY-UHFFFAOYSA-N octadecanoic acid;propane-1,2,3-triol Chemical compound OCC(O)CO.CCCCCCCCCCCCCCCCCC(O)=O CKQVRZJOMJRTOY-UHFFFAOYSA-N 0.000 description 1
- 229940116918 octadecenedioic acid Drugs 0.000 description 1
- UHGIMQLJWRAPLT-UHFFFAOYSA-N octadecyl dihydrogen phosphate Chemical compound CCCCCCCCCCCCCCCCCCOP(O)(O)=O UHGIMQLJWRAPLT-UHFFFAOYSA-N 0.000 description 1
- 229960002446 octanoic acid Drugs 0.000 description 1
- 229960003921 octisalate Drugs 0.000 description 1
- 229940073665 octyldodecyl myristate Drugs 0.000 description 1
- 239000004533 oil dispersion Substances 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 239000012044 organic layer Substances 0.000 description 1
- 239000012860 organic pigment Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 230000004792 oxidative damage Effects 0.000 description 1
- NDLPOXTZKUMGOV-UHFFFAOYSA-N oxo(oxoferriooxy)iron hydrate Chemical compound O.O=[Fe]O[Fe]=O NDLPOXTZKUMGOV-UHFFFAOYSA-N 0.000 description 1
- DXGLGDHPHMLXJC-UHFFFAOYSA-N oxybenzone Chemical group OC1=CC(OC)=CC=C1C(=O)C1=CC=CC=C1 DXGLGDHPHMLXJC-UHFFFAOYSA-N 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical compound [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 description 1
- LXTZRIBXKVRLOA-UHFFFAOYSA-N padimate a Chemical compound CCCCCOC(=O)C1=CC=C(N(C)C)C=C1 LXTZRIBXKVRLOA-UHFFFAOYSA-N 0.000 description 1
- 210000002741 palatine tonsil Anatomy 0.000 description 1
- 239000001688 paprika extract Substances 0.000 description 1
- 235000012658 paprika extract Nutrition 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 235000019809 paraffin wax Nutrition 0.000 description 1
- 235000011837 pasties Nutrition 0.000 description 1
- 239000000312 peanut oil Substances 0.000 description 1
- 229940016593 peg-20 glyceryl isostearate Drugs 0.000 description 1
- 229940031709 peg-30-dipolyhydroxystearate Drugs 0.000 description 1
- 229940089510 peg-4 stearate Drugs 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- 239000000825 pharmaceutical preparation Substances 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- 229960005323 phenoxyethanol Drugs 0.000 description 1
- 229940057874 phenyl trimethicone Drugs 0.000 description 1
- 235000011765 phytoene Nutrition 0.000 description 1
- 230000019612 pigmentation Effects 0.000 description 1
- ONJQDTZCDSESIW-UHFFFAOYSA-N polidocanol Chemical compound CCCCCCCCCCCCOCCOCCOCCOCCOCCOCCOCCOCCOCCO ONJQDTZCDSESIW-UHFFFAOYSA-N 0.000 description 1
- 229920001983 poloxamer Polymers 0.000 description 1
- 229960000502 poloxamer Drugs 0.000 description 1
- 229920003216 poly(methylphenylsiloxane) Polymers 0.000 description 1
- 229920001281 polyalkylene Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229940100518 polyglyceryl-4 isostearate Drugs 0.000 description 1
- 239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 description 1
- 235000010486 polyoxyethylene sorbitan monolaurate Nutrition 0.000 description 1
- 239000001818 polyoxyethylene sorbitan monostearate Substances 0.000 description 1
- 235000010989 polyoxyethylene sorbitan monostearate Nutrition 0.000 description 1
- 229920002503 polyoxyethylene-polyoxypropylene Polymers 0.000 description 1
- 229940068977 polysorbate 20 Drugs 0.000 description 1
- 229940113124 polysorbate 60 Drugs 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- RMGVATURDVPNOZ-UHFFFAOYSA-M potassium;hexadecyl hydrogen phosphate Chemical compound [K+].CCCCCCCCCCCCCCCCOP(O)([O-])=O RMGVATURDVPNOZ-UHFFFAOYSA-M 0.000 description 1
- ANBFRLKBEIFNQU-UHFFFAOYSA-M potassium;octadecanoate Polymers [K+].CCCCCCCCCCCCCCCCCC([O-])=O ANBFRLKBEIFNQU-UHFFFAOYSA-M 0.000 description 1
- PZQSQRCNMZGWFT-QXMHVHEDSA-N propan-2-yl (z)-octadec-9-enoate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC(C)C PZQSQRCNMZGWFT-QXMHVHEDSA-N 0.000 description 1
- ZPWFUIUNWDIYCJ-UHFFFAOYSA-N propan-2-yl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC(C)C ZPWFUIUNWDIYCJ-UHFFFAOYSA-N 0.000 description 1
- 125000004368 propenyl group Chemical group C(=CC)* 0.000 description 1
- 229960003415 propylparaben Drugs 0.000 description 1
- 229940079889 pyrrolidonecarboxylic acid Drugs 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- ARIWANIATODDMH-UHFFFAOYSA-N rac-1-monolauroylglycerol Chemical compound CCCCCCCCCCCC(=O)OCC(O)CO ARIWANIATODDMH-UHFFFAOYSA-N 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 238000007665 sagging Methods 0.000 description 1
- 238000007127 saponification reaction Methods 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 230000001235 sensitizing effect Effects 0.000 description 1
- 230000001953 sensory effect Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 229940057910 shea butter Drugs 0.000 description 1
- 150000004756 silanes Chemical class 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 229940083037 simethicone Drugs 0.000 description 1
- 201000000849 skin cancer Diseases 0.000 description 1
- 208000017520 skin disease Diseases 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- GCLGEJMYGQKIIW-UHFFFAOYSA-H sodium hexametaphosphate Chemical compound [Na]OP1(=O)OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])O1 GCLGEJMYGQKIIW-UHFFFAOYSA-H 0.000 description 1
- 235000019982 sodium hexametaphosphate Nutrition 0.000 description 1
- 239000001540 sodium lactate Substances 0.000 description 1
- 229940005581 sodium lactate Drugs 0.000 description 1
- 235000011088 sodium lactate Nutrition 0.000 description 1
- 235000019983 sodium metaphosphate Nutrition 0.000 description 1
- RYYKJJJTJZKILX-UHFFFAOYSA-M sodium octadecanoate Polymers [Na+].CCCCCCCCCCCCCCCCCC([O-])=O RYYKJJJTJZKILX-UHFFFAOYSA-M 0.000 description 1
- 229940080313 sodium starch Drugs 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
- 229960005078 sorbitan sesquioleate Drugs 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 229940032094 squalane Drugs 0.000 description 1
- 229940031439 squalene Drugs 0.000 description 1
- TUHBEKDERLKLEC-UHFFFAOYSA-N squalene Natural products CC(=CCCC(=CCCC(=CCCC=C(/C)CCC=C(/C)CC=C(C)C)C)C)C TUHBEKDERLKLEC-UHFFFAOYSA-N 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 229940100459 steareth-20 Drugs 0.000 description 1
- 229940100458 steareth-21 Drugs 0.000 description 1
- 125000004079 stearyl group Chemical group [H]C([*])([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])C([H])([H])C([H])([H])[H] 0.000 description 1
- ABTZKZVAJTXGNN-UHFFFAOYSA-N stearyl heptanoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CCCCCC ABTZKZVAJTXGNN-UHFFFAOYSA-N 0.000 description 1
- 229940098758 stearyl heptanoate Drugs 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 230000035882 stress Effects 0.000 description 1
- 239000002600 sunflower oil Substances 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 229940095064 tartrate Drugs 0.000 description 1
- 229960003080 taurine Drugs 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 239000001577 tetrasodium phosphonato phosphate Substances 0.000 description 1
- GYBINGQBXROMRS-UHFFFAOYSA-J tetrasodium;2-(1,2-dicarboxylatoethylamino)butanedioate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]C(=O)CC(C([O-])=O)NC(C([O-])=O)CC([O-])=O GYBINGQBXROMRS-UHFFFAOYSA-J 0.000 description 1
- 229960002663 thioctic acid Drugs 0.000 description 1
- 239000010496 thistle oil Substances 0.000 description 1
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 1
- 229910001887 tin oxide Inorganic materials 0.000 description 1
- XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- 230000000699 topical effect Effects 0.000 description 1
- 238000002834 transmittance Methods 0.000 description 1
- 150000003626 triacylglycerols Chemical class 0.000 description 1
- 150000003918 triazines Chemical class 0.000 description 1
- 229940093609 tricaprylin Drugs 0.000 description 1
- OYGYKEULCAINCL-UHFFFAOYSA-N triethoxy(hexadecyl)silane Chemical compound CCCCCCCCCCCCCCCC[Si](OCC)(OCC)OCC OYGYKEULCAINCL-UHFFFAOYSA-N 0.000 description 1
- NBXZNTLFQLUFES-UHFFFAOYSA-N triethoxy(propyl)silane Chemical compound CCC[Si](OCC)(OCC)OCC NBXZNTLFQLUFES-UHFFFAOYSA-N 0.000 description 1
- 229940098385 triisostearin Drugs 0.000 description 1
- HQYALQRYBUJWDH-UHFFFAOYSA-N trimethoxy(propyl)silane Chemical compound CCC[Si](OC)(OC)OC HQYALQRYBUJWDH-UHFFFAOYSA-N 0.000 description 1
- LINXHFKHZLOLEI-UHFFFAOYSA-N trimethyl-[phenyl-bis(trimethylsilyloxy)silyl]oxysilane Chemical compound C[Si](C)(C)O[Si](O[Si](C)(C)C)(O[Si](C)(C)C)C1=CC=CC=C1 LINXHFKHZLOLEI-UHFFFAOYSA-N 0.000 description 1
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- VLPFTAMPNXLGLX-UHFFFAOYSA-N trioctanoin Chemical compound CCCCCCCC(=O)OCC(OC(=O)CCCCCCC)COC(=O)CCCCCCC VLPFTAMPNXLGLX-UHFFFAOYSA-N 0.000 description 1
- SMYKBXMWXCZOLU-UHFFFAOYSA-N tris-decyl benzene-1,2,4-tricarboxylate Chemical compound CCCCCCCCCCOC(=O)C1=CC=C(C(=O)OCCCCCCCCCC)C(C(=O)OCCCCCCCCCC)=C1 SMYKBXMWXCZOLU-UHFFFAOYSA-N 0.000 description 1
- 235000013799 ultramarine blue Nutrition 0.000 description 1
- 238000009827 uniform distribution Methods 0.000 description 1
- 125000004417 unsaturated alkyl group Chemical group 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- NCYCYZXNIZJOKI-UHFFFAOYSA-N vitamin A aldehyde Natural products O=CC=C(C)C=CC=C(C)C=CC1=C(C)CCCC1(C)C NCYCYZXNIZJOKI-UHFFFAOYSA-N 0.000 description 1
- 150000003722 vitamin derivatives Chemical class 0.000 description 1
- VHBFFQKBGNRLFZ-UHFFFAOYSA-N vitamin p Natural products O1C2=CC=CC=C2C(=O)C=C1C1=CC=CC=C1 VHBFFQKBGNRLFZ-UHFFFAOYSA-N 0.000 description 1
- 239000007762 w/o emulsion Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Polymers [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 1
- 229910001928 zirconium oxide Inorganic materials 0.000 description 1
- OENHQHLEOONYIE-JLTXGRSLSA-N β-Carotene Chemical compound CC=1CCCC(C)(C)C=1\C=C\C(\C)=C\C=C\C(\C)=C\C=C\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C OENHQHLEOONYIE-JLTXGRSLSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01G—COMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
- C01G23/00—Compounds of titanium
- C01G23/04—Oxides; Hydroxides
- C01G23/047—Titanium dioxide
- C01G23/053—Producing by wet processes, e.g. hydrolysing titanium salts
-
- 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
- C08K9/00—Use of pretreated ingredients
- C08K9/04—Ingredients treated with organic substances
- C08K9/06—Ingredients treated with organic substances with silicon-containing compounds
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01G—COMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
- C01G23/00—Compounds of titanium
- C01G23/04—Oxides; Hydroxides
- C01G23/047—Titanium dioxide
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01G—COMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
- C01G23/00—Compounds of titanium
- C01G23/04—Oxides; Hydroxides
- C01G23/047—Titanium dioxide
- C01G23/08—Drying; Calcining ; After treatment of titanium oxide
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09C—TREATMENT OF INORGANIC MATERIALS, OTHER THAN FIBROUS FILLERS, TO ENHANCE THEIR PIGMENTING OR FILLING PROPERTIES ; PREPARATION OF CARBON BLACK ; PREPARATION OF INORGANIC MATERIALS WHICH ARE NO SINGLE CHEMICAL COMPOUNDS AND WHICH ARE MAINLY USED AS PIGMENTS OR FILLERS
- C09C1/00—Treatment of specific inorganic materials other than fibrous fillers; Preparation of carbon black
- C09C1/36—Compounds of titanium
- C09C1/3607—Titanium dioxide
- C09C1/3684—Treatment with organo-silicon compounds
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2006/00—Physical properties of inorganic compounds
- C01P2006/11—Powder tap density
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2006/00—Physical properties of inorganic compounds
- C01P2006/12—Surface area
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Environmental & Geological Engineering (AREA)
- General Life Sciences & Earth Sciences (AREA)
- Geology (AREA)
- Inorganic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Cosmetics (AREA)
- Inorganic Compounds Of Heavy Metals (AREA)
- Catalysts (AREA)
- Pigments, Carbon Blacks, Or Wood Stains (AREA)
- Silicon Compounds (AREA)
- Medicinal Preparation (AREA)
Description
− 該二酸化チタンを用いて製造された日焼け防止用配合物は、皮膚に施与した際に透明度が不十分であること(”白塗り”)。
− 複雑な分散液が必要であること。
− 例えば化粧用油又は水中の分散液に対する顕著な増粘効果によって、高いTiO2含分を有する分散液又は日焼け防止剤の製造が困難となること。
− 該二酸化チタンを用いて製造された日焼け防止用配合物は皮膚の上で鈍い感触を示すこと。
a)(RO)3Si(CnH2n+1)及び(RO)3Si(CnH2n−1)の型のオルガノシラン
R=アルキル、例えばメチル、エチル、n−プロピル、イソプロピル、ブチル、
n=1〜20、
b)R’x(RO)ySi(CnH2n+1)及びR’x(RO)ySi(CnH2n−1)の型のオルガノシラン
R=アルキル、例えばメチル、エチル、n−プロピル、イソプロピル、ブチル、
R’=アルキル、例えばメチル、エチル、n−プロピル、イソプロピル、ブチル、
R’=シクロアルキル、
n=1〜20、
x+y=3、
x=1、2、
y=1、2、
c)X3Si(CnH2n+1)及びX3Si(CnH2n−1)の型のハロオルガノシラン
X=Cl、Br
n=1〜20、
d)X2(R’)Si(CnH2n+1)及びX2(R’)Si(CnH2n−1)の型のハロオルガノシラン
X=Cl、Br
R’=アルキル、例えばメチル、エチル、n−プロピル、イソプロピル、ブチル、
R’=シクロアルキル、
n=1〜20、
e)X(R’)2Si(CnH2n+1)及びX(R’)2Si(CnH2n−1)の型のハロオルガノシラン
X=Cl、Br
R’=アルキル、例えばメチル、エチル、n−プロピル、イソプロピル、ブチル、
R’=シクロアルキル、
n=1〜20、
f)(RO)3Si(CH2)m−R’型のオルガノシラン
R=アルキル、例えばメチル、エチル、プロピル、
m=0.1〜20、
R’=メチル、アリール(例えば−C6H5、置換されたフェニル基)
−C4F9、OCF2−CHF−CF3、−C6F13、−O−CF2−CHF2
−NH2、−N3、−SCN、−CH=CH2、−NH−CH2−CH2−NH2、
−N−(CH2−CH2−NH2)2
−OOC(CH3)C=CH2
−OCH2−CH(O)CH2
−NH−CO−N−CO−(CH2)5
−NH−COO−CH3、−NH−COO−CH2−CH3、−NH−(CH2)3Si(OR)3
−Sx−(CH2)3Si(OR)3
−SH
−NR’R’’R’’’(R’=アルキル、アリール;R’’=H、アルキル、アリール;R’’’=H、アルキル、アリール、ベンジル、C2H4NR’’’’R’’’’’、ここで、R’’’’=H、アルキル及びR’’’’’=H、アルキル)
g)(R’’)x(RO)ySi(CH2)m−R’型のオルガノシラン
R’’=アルキル x+y=3
=シクロアルキル x=1、2
y=1、2
m=0.1〜20
R’=メチル、アリール(例えば−C6H5、置換されたフェニル基)
−C4F9、OCF2−CHF−CF3、−C6F13、−O−CF2−CHF2
−NH2、−N3、−SCN、−CH=CH2、−NH−CH2−CH2−NH2、
−N−(CH2−CH2−NH2)2
−OOC(CH3)C=CH2
−OCH2−CH(O)CH2
−NH−CO−N−CO−(CH2)5
−NH−COO−CH3、−NH−COO−CH2−CH3、−NH−(CH2)3Si(OR)3
−Sx−(CH2)3Si(OR)3
−SH
−NR’R’’R’’’(R’=アルキル、アリール;R’’=H、アルキル、アリール;R’’’=H、アルキル、アリール、ベンジル、C2H4NR’’’’R’’’’’、ここで、R’’’’=H、アルキル及びR’’’’’=H、アルキル)
h)X3Si(CH2)m−R’型のハロオルガノシラン
X=Cl、Br、
m=0.1〜20
R’=メチル、アリール(例えば−C6H5、置換されたフェニル基)
−C4F9、OCF2−CHF−CF3、−C6F13、−O−CF2−CHF2
−NH2、−N3、−SCN、−CH=CH2、
−NH−CH2−CH2−NH2
−N−(CH2−CH2−NH2)2
−OOC(CH3)C=CH2
−OCH2−CH(O)CH2
−NH−CO−N−CO−(CH2)5
−NH−COO−CH3、−NH−COO−CH2−CH3、−NH−(CH2)3Si(OR)3
−Sx−(CH2)3Si(OR)3
−SH
i)(R)X2Si(CH2)m−R’型のハロオルガノシラン
X=Cl、Br、
R=アルキル、例えばメチル、エチル、プロピル、
m=0.1〜20
R’=メチル、アリール(例えば−C6H5、置換されたフェニル基)
−C4F9、OCF2−CHF−CF3、−C6F13、−O−CF2−CHF2
−NH2、−N3、−SCN、−CH=CH2、−NH−CH2−CH2−NH2、
−N−(CH2−CH2−NH2)2
−OOC(CH3)C=CH2
−OCH2−CH(O)CH2
−NH−CO−N−CO−(CH2)5
−NH−COO−CH3、−NH−COO−CH2−CH3、−NH−(CH2)3Si(OR)3、ここで、Rはメチル、エチル、プロピル、ブチルであってよい、
−Sx−(CH2)3Si(OR)3、ここで、Rはメチル、エチル、プロピル、ブチルであってよい、
−SH
j)(R)2XSi(CH2)m−R’型のハロオルガノシラン
X=Cl、Br、
R=アルキル、
m=0.1〜20
R’=メチル、アリール(例えば−C6H5、置換されたフェニル基)
−C4F9、OCF2−CHF−CF3、−C6F13、−O−CF2−CHF2
−NH2、−N3、−SCN、−CH=CH2、−NH−CH2−CH2−NH2、
−N−(CH2−CH2−NH2)2
−OOC(CH3)C=CH2
−OCH2−CH(O)CH2
−NH−CO−N−CO−(CH2)5
−NH−COO−CH3、−NH−COO−CH2−CH3、−NH−(CH2)3Si(OR)3
−Sx−(CH2)3Si(OR)3
−SH
k)以下の型
R=アルキル、ビニル、アリール、
R’=アルキル、ビニル、アリール、
l)D3、D4、D5の型の環式ポリシロキサン、ここで、D3、D4及びD5は−O−Si(CH3)2−の型の単位を3、4又は5個有する環式ポリシロキサンであると理解される。例えばオクタメチルシクロテトラシロキサン=D4である
R=アルキル、例えばCnH2n+1(但しn=1〜20)、アリール、例えばフェニル及び置換されたフェニル基、(CH2)n−NH2、H、
R’=アルキル、例えばCnH2n+1(但しn=1〜20)、アリール、例えばフェニル及び置換されたフェニル基、(CH2)n−NH2、H、
R’’=アルキル、例えばCnH2n+1(但しn=1〜20)、アリール、例えばフェニル及び置換されたフェニル基、(CH2)n−NH2、H、
R’’’=アルキル、例えばCnH2n+1(但しn=1〜20)、アリール、例えばフェニル及び置換されたフェニル基、(CH2)n−NH2、H。
− 前記粉末は0.5〜40質量%の二酸化ケイ素の量を含有する。
− 前記粉末は5〜300m2/gのBET表面積を有する、及び
− 前記粉末は二酸化ケイ素のシェル及び二酸化チタンのコアを有する一次粒子から成る。
− 該乳化剤の親油性は、温度を上昇させることによって親油性が増加し、かつ温度を低下させることによって該乳化剤の親油性が減少するというように温度に依存している。
− ≦8のHLB価を有する少なくとも1種のシリコーン乳化剤(W/S)及び/又は<7のHLB価を有する少なくとも1種のW/O乳化剤
を含むW/O又はW/Sエマルション、及び
>10のHLB価を有する少なくとも1種のO/W乳化剤である。
A)10〜40個の炭素原子の鎖長を有する、完全に中和された、部分的に中和された、又は中和されていない、分枝鎖及び/又は非分枝鎖、飽和及び/又は不飽和の脂肪酸の群から選択された少なくとも1種の乳化剤A
B)10〜40個の炭素原子の鎖長を有し、かつ5〜100のエトキシル化の程度を有する、ポリエトキシル化脂肪酸エステルの群から選択された少なくとも1種の乳化剤B、及び
C)10〜40個の炭素原子の鎖長を有する、飽和及び/又は不飽和、分枝鎖及び/又は非分枝鎖の脂肪アルコールの群から選択された少なくとも1種の共乳化剤C
から成る乳化剤系を含有する。
− 二酸化チタン(被覆又は未被覆):例えばMerck社製のEusolex T-2000、Tayca Corporation社製の二酸化チタンMT 100 Z
− 酸化亜鉛、例えばBASF AG社製のZ-Cote及びZ-Cote HP1、Tayca Corporation社製のMZ-300、MZ-500及びMZ-505M
− 酸化鉄。
a)単位R2SiO及びRSiO1.5及び/又はR3SiO0.5及び/又はSiO2を含有するシロキサンエラストマー、ここで、個々の基Rはそれぞれ他と独立して水素、C1−24−アルキル(例えばメチル、エチル、プロピル)又はアリール(例えばフェニル又はトリル)、アルケニル(例えばビニル)を表し、かつ単位R2SiO:RSiO1.5の質量比は1:1〜30:1の範囲から選択されている。
− オルガノポリシロキサンが非環式である場合には1〜20モル%の範囲内であり、かつ
− オルガノポリシロキサンが環式である場合には1〜50モル%の範囲内であるように選択される。
1.天然真珠光沢顔料、例えば
−「フィッシュシルバー」(魚鱗からのグアニン/ヒポキサンチン混合結晶体)及び
−「真珠質」(粉砕イガイ殻)
2.単結晶真珠光沢顔料、例えばオキシ塩化ビスマス(BiOCl)。
3.層基体顔料:例えば雲母/金属酸化物。
− フェニレン−1,4−ビス−(2−ベンズイミダジル)−3,3’−5,5’−テトラスルホン酸及びその塩、特に相応するナトリウム、カリウム又はトリエタノールアンモニウム塩、特に、INCI名称フェニルジベンゾイミダゾールテトラスルホン酸二ナトリウム(CAS番号:180898−37−7)を有するフェニレン−1,4−ビス−(2−ベンズイミダジル)−3,3’−5,5’−テトラスルホン酸ビスナトリウム塩、これは例えばHaarmann & Reimer社からNeo Heliopan APの商品名で入手可能である;
− 2−フェニルベンゾイミダゾール−5−スルホン酸の塩、例えばそのナトリウム、カリウム又はトリエタノールアンモニウム塩、並びに、INCI名称フェニルベンゾイミダゾールスルホン酸(CAS番号:27503−81−7)を有するスルホン酸自体、これは例えばMerck社からEusolex 232の商品名で、又はHaarmann & Reimer社からNeo Heliopan Hydroの商品名で入手可能である;
− 1,4−ジ(2−オキソ−10−スルホ−3−ボルニリデンメチル)−ベンゼン(また以下のようにも呼称される:3,3’−(1,4−フェニレンジメチレン)−ビス−(7,7−ジメチル−2−オキソ−ビシクロ−[2.2.1]ヘプト−1−イルメタンスルホン酸)及びその塩(特に相応する10−スルファト化合物、特に相応するナトリウム、カリウム又はトリエタノールアンモニウム塩)、これはベンゼン−1,4−ジ(2−オキソ−3−ボルニリデンメチル−10−スルホン酸)とも呼称される。ベンゼン−1,4−ジ(2−オキソ−3−ボルニリデンメチル−10−スルホン酸)はINCI名称テレフタリデンジカンファースルホン酸(CAS番号:90457−82−2)を有し、かつ例えばChimex社からMexoryl SXの商品名で入手可能である;
− 3−ベンジリデンカンファーのスルホン酸誘導体、例えば4−(2−オキソ−3−ボルニリデンメチル)ベンゼンスルホン酸、2−メチル−5−(2−オキソ−3−ボルニリデンメチル)スルホン酸及びその塩。
R1、R2及びR3は相互に独立して、1〜10個の炭素原子を有する分枝鎖又は非分枝鎖の飽和又は不飽和アルキル基の群から選択される]
により特徴付けられるベンゾオキサゾール誘導体も本発明の範囲内で有利なUVフィルター物質である。基R1及びR2が同じであって、特に3〜5個の炭素原子を有する分枝鎖アルキル基の群からのものであるように選択することは、本発明によれば特に有利である。R3が8個の炭素原子を有する非分枝鎖又は分枝鎖アルキル基、特に2−エチルヘキシル基を表す場合も本発明の範囲内で特に有利である。
− R1及びR2は相互に独立して水素、C1−20−アルキル、C3−10−シクロアルキル又はC3−10−シクロアルケニルを表し、ここで、基R1及びR2は該基が結合している窒素原子と一緒に5員又は6員の環を形成してよく、かつ
− R3はC1−20−アルキル基を表す]
により特徴付けられる。
− 2,4−ビス−[4−(2−エチル−ヘキシルオキシ)−2−ヒドロキシ]−フェニル−6−(4−メトキシフェニル)−1,3,5−トリアジン(INCI:ビス−エチルヘキシルオキシルフェノールメトキシフェニルトリアジン)、これはCIBA-Chemikalien GmbH社からTinosorb TM Sの商品名で入手可能である;
− ジオクチルブチルアミドトリアゾン(INCI:ジエチルヘキシルブタミドトリアゾン)、これはSigma 3 V社からUVASORB HEBの商品名で入手可能である;
− 4,4’,4’’−(1,3,5−トリアジン−2,4,6−トリイルトリアミノ)−トリス−安息香酸トリス(2−エチルヘキシルエステル)、また以下のようにも呼称される:2,4,6−トリス−[アニリノ−(p−カルボ−2’−エチル−1’−ヘキシルオキシ)]−1,3,5−トリアジン(INCI:エチルヘキシルトリアゾン)、これはBASF Aktiengesellschaft社からUVINUL TM T 150の商品名で市販されている;
− 2−[4,6−ビス(2,4−ジメチルフェニル)−1,3,5−トリアジン−2−イル]−5−(オクチルオキシ)フェノール(CAS番号:2725−22−6)。
− 3−ベンジリデンカンファー誘導体、有利に3−(4−メチルベンジリデン)カンファー、3−ベンジリデンカンファー;
− 4−アミノ安息香酸誘導体、有利に4−(ジメチルアミノ)−安息香酸(2−エチルヘキシル)エステル、4−(ジメチルアミノ)安息香酸アミルエステル;
− 2,4,6−トリアニリノ−(p−カルボ−2’−エチル−1’−ヘキシルオキシ)−1,3,5−トリアジン;
− ベンザルマロン酸のエステル、有利に4−メトキシベンザルマロン酸ジ(2−エチルヘキシル)エステル;
− ケイ皮酸のエステル、有利に4−メトキシケイ皮酸(2−エチルヘキシル)エステル、4−メトキシケイ皮酸イソペンチルエステル;
− ベンゾフェノンの誘導体、有利に2−ヒドロキシ−4−メトキシベンゾフェノン、2−ヒドロキシ−4−メトキシ−4’−メチルベンゾフェノン、2,2’−ジヒドロキシ−4−メトキシベンゾフェノン、及び
− ポリマーに結合したUVフィルター。
x、y及びzは2〜130、特に15〜100の範囲内の整数を表し、かつx及びzは同じであるが但しyとは独立して選択される]
を有する水溶性又は水分散性ポリオキシエチレン−ポリオキシプロピレンブロックポリマー(CTFA名称:ポラキサマー(polaxamer)、CAS番号:9003−11−6)である。
以下の試薬を表面変性剤として使用することができる:
プロピルトリメトキシシラン、プロピルトリエトキシシラン、オクチルトリメトキシシラン(OCTMO)、オクチルトリエトキシシラン、ヘキサデシルトリメトキシシラン、ヘキサデシルトリエトキシシラン、ジメチルポリシロキサン。オクチルトリメトキシシラン及びオクチルトリエトキシシランの使用が特に有利である。
1.表面変性
出発材料として、WO2004/056927により製造される熱分解により製造された二酸化ケイ素−二酸化チタン混合酸化物を使用する。
分散液の製造
TEGOSOFT(登録商標)TN278.25gを500mlのPEビーカー内に装入し、試験すべき二酸化チタン粉末21.75gを溶解機(Pendraulik type LM34 No. 29490、ディスク直径6cm)を用いて470rpmで撹拌し、その後、3000rpmで5分間分散させる。
7.25質量%分散液の透明度をData Color SF600 Plus分光光度計を用いて測定する。分散液を12μmスパイラルブレードを用いてErichsen Testing Equipment K Control Coater施与装置、施与速度2を用いて、ラッカー塗装された黒色厚紙に施与する。施与1回につき3つの測定点を測定する。前記の3つの測定値の平均を算出する。装置を保護するために、測定をディスタンスリングを用いて行う。
3質量%分散液のUV−Visスペクトルを、取外し可能な10μm石英ガラスセル中で、光度計球を有するSpecord 200 UV-Vis分光光度計(Analytik Jena AG)を用いて測定する。この目的のために、上記の油性分散液をTego-soft TNで希釈する。
粘度をブルックフィールドレオメーターRVDV-III+cPを用いて測定する。測定を、RVスピンドルセットを有するPE混合ビーカー(350ml)中で10rpmで実施する。1分後、値をmPasで読み取る。/分、1分後)
施与に関する試験の結果
− 改善された透明度
− 320nmでの比較可能な透過率又は吸収
− 380nmでの増加した透過率及びそれに応じて低減した白塗り
− 低減した増粘作用。これにより高度に充填された分散液の製造が可能になる。
− 改善された透明度
− 320nmでの比較可能な透過率又は吸収
− 380nmでの増加した透過率及びそれに応じて低減した白塗り
− 若干の場合において著しく低減した増粘作用。これにより高度に充填された分散液の製造が可能になる。
Claims (5)
- シランで表面変性された、二酸化ケイ素で被覆され熱分解により製造された二酸化チタンであって、前記シランが、
a)(RO)3Si(CnH2n+1)及び(RO)3Si(CnH2n−1)の型のオルガノシラン(式中、R=アルキル、n=1〜20を示す。)、
b)R’x(RO)ySi(CnH2n+1)及びR’x(RO)ySi(CnH2n−1)の型のオルガノシラン(式中、R=アルキル、R’=アルキルまたはシクロアルキル、n=1〜20、x+y=3、x=1、2、y=1、2を示す。)、
c)X3Si(CnH2n+1)及びX3Si(CnH2n−1)の型のハロオルガノシラン(式中、X=Cl、Br、n=1〜20を示す)、
d)X2(R’)Si(CnH2n+1)及びX2(R’)Si(CnH2n−1)の型のハロオルガノシラン(式中、X=Cl、Br、R’=アルキルまたはシクロアルキル、n=1〜20を示す。)、
e)X(R’)2Si(CnH2n+1)及びX(R’)2Si(CnH2n−1)の型のハロオルガノシラン(式中、X=Cl、Br、R’=アルキルまたはシクロアルキル、n=1〜20を示す。)、
f)(RO)3Si(CH2)m−R’型のオルガノシラン
(式中、R=アルキル、m=0または1〜20、
R’=メチル、アリール
−C4F9、−OCF2−CHF−CF3、−C6F13、−O−CF2−CHF2
−NH2、−N3、−SCN、−CH=CH2、−NH−CH2−CH2−NH2、
−N−(CH2−CH2−NH2)2
−OOC(CH3)C=CH 2
−NH−COO−CH3、−NH−COO−CH2−CH3、−NH−(CH2)3Si(OR)3 (式中、R=アルキルを示す。)
−Sx−(CH2)3Si(OR)3 (式中、R=アルキル、x=1または2を示す。)
−SH
g)(R’’)x(RO)ySi(CH2)m−R’型のオルガノシラン
(式中、
R’’=アルキルまたはシクロアルキルであり、x=1または2、y=1または2、x+y=3、m=0または1〜20
R’=メチル、アリール
−C4F9、−OCF2−CHF−CF3、−C6F13、−O−CF2−CHF2
−NH2、−N3、−SCN、−CH=CH2、−NH−CH2−CH2−NH2、
−N−(CH2−CH2−NH2)2
−OOC(CH3)C=CH 2
−NH−COO−CH3、−NH−COO−CH2−CH3、−NH−(CH2)3Si(OR)3 (式中、R=アルキルを示す。)
−Sx−(CH2)3Si(OR)3 (式中、R=アルキル、x=1または2を示す。)
−SH
−NR’R’’R’’’(R’=アルキル、アリール;R’’=H、アルキル、アリール;R’’’=H、アルキル、アリール、ベンジル、C2H4NR’’’’R’’’’’、ここで、R’’’’=H、アルキル及びR’’’’’=H、アルキル)を示す。)、
h)X3Si(CH2)m−R’型のハロオルガノシラン
(式中、X=Cl、Br、m=0または1〜20
R’=メチル、アリール
−C4F9、−OCF2−CHF−CF3、−C6F13、−O−CF2−CHF2
−NH2、−N3、−SCN、−CH=CH2、
−NH−CH2−CH2−NH2
−N−(CH2−CH2−NH2)2
−OOC(CH3)C=CH 2
−NH−COO−CH3、−NH−COO−CH2−CH3、−NH−(CH2)3Si(OR)3 (式中、R=アルキルを示す。)
−Sx−(CH2)3Si(OR)3 (式中、R=アルキル、x=1または2を示す。)
−SHを示す。)、
i)(R)X2Si(CH2)m−R’型のハロオルガノシラン
(式中、X=Cl、Br、R=アルキル、m=0または1〜20
R’=メチル、アリール
−C4F9、−OCF2−CHF−CF3、−C6F13、−O−CF2−CHF2
−NH2、−N3、−SCN、−CH=CH2、−NH−CH2−CH2−NH2、
−N−(CH2−CH2−NH2)2
−OOC(CH3)C=CH 2
−NH−COO−CH3、−NH−COO−CH2−CH3、−NH−(CH2)3Si(OR)3、ここで、R=アルキルを示す、
−Sx−(CH2)3Si(OR)3、ここで、R=アルキル、x=1または2を示す、
−SHを示す。)、
j)(R)2XSi(CH2)m−R’型のハロオルガノシラン
(式中、X=Cl、Br、R=アルキル、m=0または1〜20
R’=メチル、アリール
−C4F9、−OCF2−CHF−CF3、−C6F13、−O−CF2−CHF2
−NH2、−N3、−SCN、−CH=CH2、−NH−CH2−CH2−NH2、
−N−(CH2−CH2−NH2)2
−OOC(CH3)C=CH 2
−NH−COO−CH3、−NH−COO−CH2−CH3、−NH−(CH2)3Si(OR)3 (式中、R=アルキルを示す。)
−Sx−(CH2)3Si(OR)3 (式中、R=アルキル、x=1または2を示す。)
−SHを示す。)、
k)以下の型
(式中、R=アルキル、ビニル、アリール、R’=アルキル、ビニル、アリールを示す。)、
l)D3、D4、D5の型の環式ポリシロキサン、ここで、D3、D4及びD5は−O−Si(CH3)2−の型の単位を3、4又は5個有する環式ポリシロキサンである、
及びm)以下の型
(式中、R=アルキル、アリール、H、R’=アルキル、アリール、H、R’’=アルキル、アリール、H、
R’’’=アルキル、アリール、Hを示す。)からなる群から選択された少なくとも1種のシランである、二酸化ケイ素で被覆され熱分解により製造された二酸化チタン。 - 前記シランで表面変性された、請求項1記載の、二酸化ケイ素で被覆され熱分解により製造された二酸化チタンの製造法において、フレーム加水分解により製造され、かつ二酸化ケイ素で被覆された二酸化チタンに、前記シランを噴霧し、引き続き温度処理することを特徴とする製造法。
- 前記シランで表面変性された、請求項1記載の、二酸化ケイ素で被覆され熱分解により製造された二酸化チタンの製造法において、フレーム加水分解により製造され、かつ二酸化ケイ素で被覆された二酸化チタンに、第一に水を噴霧し、その後、前記シランを噴霧し、引き続き温度処理することを特徴とする製造法。
- 前記シランで表面変性された、請求項1記載の、二酸化ケイ素で被覆され熱分解により製造された二酸化チタンの製造法において、フレーム加水分解により製造され、かつ二酸化ケイ素で被覆された二酸化チタンを蒸気形の前記シランで処理し、その後熱処理することを特徴とする製造法。
- 日焼け防止用配合物において、前記シランで表面変性された、請求項1記載の、二酸化ケイ素で被覆され熱分解により製造された二酸化チタンを0.1〜25質量%の量で含有することを特徴とする日焼け防止用配合物。
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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EP04030586A EP1674517B1 (de) | 2004-12-23 | 2004-12-23 | Oberflächenmodifizierte pyrogen hergestellte Titandioxide |
EP04030586.4 | 2004-12-23 |
Publications (2)
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JP2006213915A JP2006213915A (ja) | 2006-08-17 |
JP5150051B2 true JP5150051B2 (ja) | 2013-02-20 |
Family
ID=34927950
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JP2005372186A Expired - Fee Related JP5150051B2 (ja) | 2004-12-23 | 2005-12-26 | 表面変性され、熱分解により製造された二酸化チタン |
Country Status (13)
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US (1) | US20060159635A1 (ja) |
EP (1) | EP1674517B1 (ja) |
JP (1) | JP5150051B2 (ja) |
KR (1) | KR101254491B1 (ja) |
CN (1) | CN100584897C (ja) |
AT (1) | ATE384763T1 (ja) |
AU (1) | AU2005247006B2 (ja) |
CA (1) | CA2531608C (ja) |
DE (1) | DE502004006066D1 (ja) |
ES (1) | ES2299790T3 (ja) |
MY (1) | MY141212A (ja) |
SG (1) | SG123756A1 (ja) |
TW (1) | TWI306839B (ja) |
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US20060159635A1 (en) | 2006-07-20 |
DE502004006066D1 (de) | 2008-03-13 |
MY141212A (en) | 2010-03-31 |
KR101254491B1 (ko) | 2013-04-22 |
EP1674517A1 (de) | 2006-06-28 |
CA2531608A1 (en) | 2006-06-23 |
SG123756A1 (en) | 2006-07-26 |
EP1674517B1 (de) | 2008-01-23 |
ES2299790T3 (es) | 2008-06-01 |
TWI306839B (en) | 2009-03-01 |
TW200640791A (en) | 2006-12-01 |
CA2531608C (en) | 2012-07-17 |
KR20060073485A (ko) | 2006-06-28 |
AU2005247006B2 (en) | 2008-01-24 |
JP2006213915A (ja) | 2006-08-17 |
AU2005247006A1 (en) | 2006-07-13 |
CN1800270A (zh) | 2006-07-12 |
CN100584897C (zh) | 2010-01-27 |
ATE384763T1 (de) | 2008-02-15 |
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