BRPI0619196A2 - cápsulas - Google Patents
cápsulas Download PDFInfo
- Publication number
- BRPI0619196A2 BRPI0619196A2 BRPI0619196-7A BRPI0619196A BRPI0619196A2 BR PI0619196 A2 BRPI0619196 A2 BR PI0619196A2 BR PI0619196 A BRPI0619196 A BR PI0619196A BR PI0619196 A2 BRPI0619196 A2 BR PI0619196A2
- Authority
- BR
- Brazil
- Prior art keywords
- groups
- capsule
- capsule according
- alkyl
- reactive
- Prior art date
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- 239000002775 capsule Substances 0.000 title claims abstract description 46
- 239000000835 fiber Substances 0.000 claims abstract description 20
- 239000004753 textile Substances 0.000 claims abstract description 20
- 239000002245 particle Substances 0.000 claims abstract description 19
- 239000003094 microcapsule Substances 0.000 claims description 29
- -1 2-chloroethylsulfonyl Chemical group 0.000 claims description 22
- 239000000463 material Substances 0.000 claims description 19
- 239000004744 fabric Substances 0.000 claims description 15
- 125000002091 cationic group Chemical group 0.000 claims description 13
- 239000003795 chemical substances by application Substances 0.000 claims description 10
- 239000011159 matrix material Substances 0.000 claims description 10
- 239000004480 active ingredient Substances 0.000 claims description 9
- 239000000975 dye Substances 0.000 claims description 9
- 239000000203 mixture Substances 0.000 claims description 9
- 239000000126 substance Substances 0.000 claims description 7
- 150000001875 compounds Chemical class 0.000 claims description 6
- 239000003205 fragrance Substances 0.000 claims description 5
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 claims description 4
- SPSSDDOTEZKOOV-UHFFFAOYSA-N 2,3-dichloroquinoxaline Chemical compound C1=CC=C2N=C(Cl)C(Cl)=NC2=C1 SPSSDDOTEZKOOV-UHFFFAOYSA-N 0.000 claims description 4
- OMRXVBREYFZQHU-UHFFFAOYSA-N 2,4-dichloro-1,3,5-triazine Chemical compound ClC1=NC=NC(Cl)=N1 OMRXVBREYFZQHU-UHFFFAOYSA-N 0.000 claims description 4
- SUPFNMXTAGSTIP-UHFFFAOYSA-N 2-chloro-4,6-difluoropyrimidine Chemical compound FC1=CC(F)=NC(Cl)=N1 SUPFNMXTAGSTIP-UHFFFAOYSA-N 0.000 claims description 4
- ORLGPUVJERIKLW-UHFFFAOYSA-N 5-chlorotriazine Chemical compound ClC1=CN=NN=C1 ORLGPUVJERIKLW-UHFFFAOYSA-N 0.000 claims description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 4
- 239000011149 active material Substances 0.000 claims description 4
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 239000007844 bleaching agent Substances 0.000 claims description 4
- 239000003054 catalyst Substances 0.000 claims description 4
- 239000003814 drug Substances 0.000 claims description 4
- 229920000642 polymer Polymers 0.000 claims description 4
- 125000001424 substituent group Chemical group 0.000 claims description 4
- 102000004190 Enzymes Human genes 0.000 claims description 3
- 108090000790 Enzymes Proteins 0.000 claims description 3
- 239000012190 activator Substances 0.000 claims description 3
- 230000000845 anti-microbial effect Effects 0.000 claims description 3
- 230000002538 fungal effect Effects 0.000 claims description 3
- 239000012669 liquid formulation Substances 0.000 claims description 3
- 239000000123 paper Substances 0.000 claims description 3
- 239000000049 pigment Substances 0.000 claims description 3
- GIKMWFAAEIACRF-UHFFFAOYSA-N 2,4,5-trichloropyrimidine Chemical compound ClC1=NC=C(Cl)C(Cl)=N1 GIKMWFAAEIACRF-UHFFFAOYSA-N 0.000 claims description 2
- XPVPPZLJRZSNTD-UHFFFAOYSA-N 5-fluorotriazine Chemical compound FC1=CN=NN=C1 XPVPPZLJRZSNTD-UHFFFAOYSA-N 0.000 claims description 2
- 239000006096 absorbing agent Substances 0.000 claims description 2
- 238000010521 absorption reaction Methods 0.000 claims description 2
- 230000000975 bioactive effect Effects 0.000 claims description 2
- 230000008859 change Effects 0.000 claims description 2
- 239000000084 colloidal system Substances 0.000 claims description 2
- 239000003063 flame retardant Substances 0.000 claims description 2
- 238000009472 formulation Methods 0.000 claims description 2
- 239000000077 insect repellent Substances 0.000 claims description 2
- 239000007788 liquid Substances 0.000 claims description 2
- 239000006249 magnetic particle Substances 0.000 claims description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- 125000001453 quaternary ammonium group Chemical group 0.000 claims description 2
- 239000007787 solid Substances 0.000 claims description 2
- 239000010457 zeolite Substances 0.000 claims description 2
- 239000002981 blocking agent Substances 0.000 claims 1
- 238000004040 coloring Methods 0.000 claims 1
- 239000002979 fabric softener Substances 0.000 claims 1
- 239000002184 metal Substances 0.000 claims 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims 1
- 125000000524 functional group Chemical group 0.000 abstract description 8
- 230000008021 deposition Effects 0.000 abstract description 2
- 239000011162 core material Substances 0.000 description 11
- 238000000034 method Methods 0.000 description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- 239000000178 monomer Substances 0.000 description 8
- 239000008346 aqueous phase Substances 0.000 description 7
- 150000002924 oxiranes Chemical group 0.000 description 7
- 239000000839 emulsion Substances 0.000 description 6
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 6
- 239000012071 phase Substances 0.000 description 6
- 229920000742 Cotton Polymers 0.000 description 5
- 239000011230 binding agent Substances 0.000 description 5
- 239000006229 carbon black Substances 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- 239000004215 Carbon black (E152) Substances 0.000 description 4
- 239000004971 Cross linker Substances 0.000 description 4
- 229920000858 Cyclodextrin Polymers 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- 150000001412 amines Chemical class 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- RRAFCDWBNXTKKO-UHFFFAOYSA-N eugenol Chemical compound COC1=CC(CC=C)=CC=C1O RRAFCDWBNXTKKO-UHFFFAOYSA-N 0.000 description 4
- 229930195733 hydrocarbon Natural products 0.000 description 4
- 150000002430 hydrocarbons Chemical class 0.000 description 4
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 4
- 238000006116 polymerization reaction Methods 0.000 description 4
- 238000005406 washing Methods 0.000 description 4
- 229920006107 Beetle™ Polymers 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- IVJISJACKSSFGE-UHFFFAOYSA-N formaldehyde;1,3,5-triazine-2,4,6-triamine Chemical compound O=C.NC1=NC(N)=NC(N)=N1 IVJISJACKSSFGE-UHFFFAOYSA-N 0.000 description 3
- 238000005755 formation reaction Methods 0.000 description 3
- 150000003944 halohydrins Chemical class 0.000 description 3
- 239000002105 nanoparticle Substances 0.000 description 3
- 235000019645 odor Nutrition 0.000 description 3
- HFHDHCJBZVLPGP-UHFFFAOYSA-N schardinger α-dextrin Chemical compound O1C(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(O)C2O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC2C(O)C(O)C1OC2CO HFHDHCJBZVLPGP-UHFFFAOYSA-N 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
- KUDUQBURMYMBIJ-UHFFFAOYSA-N 2-prop-2-enoyloxyethyl prop-2-enoate Chemical compound C=CC(=O)OCCOC(=O)C=C KUDUQBURMYMBIJ-UHFFFAOYSA-N 0.000 description 2
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 2
- NPBVQXIMTZKSBA-UHFFFAOYSA-N Chavibetol Natural products COC1=CC=C(CC=C)C=C1O NPBVQXIMTZKSBA-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 239000005770 Eugenol Substances 0.000 description 2
- UVMRYBDEERADNV-UHFFFAOYSA-N Pseudoeugenol Natural products COC1=CC(C(C)=C)=CC=C1O UVMRYBDEERADNV-UHFFFAOYSA-N 0.000 description 2
- NJSSICCENMLTKO-HRCBOCMUSA-N [(1r,2s,4r,5r)-3-hydroxy-4-(4-methylphenyl)sulfonyloxy-6,8-dioxabicyclo[3.2.1]octan-2-yl] 4-methylbenzenesulfonate Chemical compound C1=CC(C)=CC=C1S(=O)(=O)O[C@H]1C(O)[C@@H](OS(=O)(=O)C=2C=CC(C)=CC=2)[C@@H]2OC[C@H]1O2 NJSSICCENMLTKO-HRCBOCMUSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O ammonium group Chemical group [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
- 150000008064 anhydrides Chemical group 0.000 description 2
- 125000000129 anionic group Chemical group 0.000 description 2
- 239000013011 aqueous formulation Substances 0.000 description 2
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
- PFKFTWBEEFSNDU-UHFFFAOYSA-N carbonyldiimidazole Chemical compound C1=CN=CN1C(=O)N1C=CN=C1 PFKFTWBEEFSNDU-UHFFFAOYSA-N 0.000 description 2
- 150000007942 carboxylates Chemical class 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- GQOKIYDTHHZSCJ-UHFFFAOYSA-M dimethyl-bis(prop-2-enyl)azanium;chloride Chemical group [Cl-].C=CC[N+](C)(C)CC=C GQOKIYDTHHZSCJ-UHFFFAOYSA-M 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- 238000005538 encapsulation Methods 0.000 description 2
- 229960002217 eugenol Drugs 0.000 description 2
- 235000019253 formic acid Nutrition 0.000 description 2
- LEQAOMBKQFMDFZ-UHFFFAOYSA-N glyoxal Chemical compound O=CC=O LEQAOMBKQFMDFZ-UHFFFAOYSA-N 0.000 description 2
- 239000012948 isocyanate Substances 0.000 description 2
- 150000002513 isocyanates Chemical class 0.000 description 2
- 239000003550 marker Substances 0.000 description 2
- 238000010907 mechanical stirring Methods 0.000 description 2
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 2
- 125000005395 methacrylic acid group Chemical group 0.000 description 2
- 239000011859 microparticle Substances 0.000 description 2
- 229920000205 poly(isobutyl methacrylate) Polymers 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 230000000717 retained effect Effects 0.000 description 2
- 239000002002 slurry Substances 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- 239000000516 sunscreening agent Substances 0.000 description 2
- 125000003396 thiol group Chemical group [H]S* 0.000 description 2
- 239000007762 w/o emulsion Substances 0.000 description 2
- 210000002268 wool Anatomy 0.000 description 2
- NVKZKCWZPSNZFD-UHFFFAOYSA-N (2,5-dioxopyrrolidin-1-yl) carbonochloridate Chemical compound ClC(=O)ON1C(=O)CCC1=O NVKZKCWZPSNZFD-UHFFFAOYSA-N 0.000 description 1
- CUNWUEBNSZSNRX-RKGWDQTMSA-N (2r,3r,4r,5s)-hexane-1,2,3,4,5,6-hexol;(z)-octadec-9-enoic acid Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO.OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO.CCCCCCCC\C=C/CCCCCCCC(O)=O.CCCCCCCC\C=C/CCCCCCCC(O)=O.CCCCCCCC\C=C/CCCCCCCC(O)=O CUNWUEBNSZSNRX-RKGWDQTMSA-N 0.000 description 1
- MYWOJODOMFBVCB-UHFFFAOYSA-N 1,2,6-trimethylphenanthrene Chemical compound CC1=CC=C2C3=CC(C)=CC=C3C=CC2=C1C MYWOJODOMFBVCB-UHFFFAOYSA-N 0.000 description 1
- QLAJNZSPVITUCQ-UHFFFAOYSA-N 1,3,2-dioxathietane 2,2-dioxide Chemical compound O=S1(=O)OCO1 QLAJNZSPVITUCQ-UHFFFAOYSA-N 0.000 description 1
- 150000003923 2,5-pyrrolediones Chemical class 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- JJBFVQSGPLGDNX-UHFFFAOYSA-N 2-(2-methylprop-2-enoyloxy)propyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC(C)COC(=O)C(C)=C JJBFVQSGPLGDNX-UHFFFAOYSA-N 0.000 description 1
- ZXIYZDSEASMXPI-UHFFFAOYSA-N 2-(methylamino)ethane-1,1,1-triol Chemical compound CNCC(O)(O)O ZXIYZDSEASMXPI-UHFFFAOYSA-N 0.000 description 1
- SLAMLWHELXOEJZ-UHFFFAOYSA-N 2-nitrobenzoic acid Chemical compound OC(=O)C1=CC=CC=C1[N+]([O-])=O SLAMLWHELXOEJZ-UHFFFAOYSA-N 0.000 description 1
- ZEYUSQVGRCPBPG-UHFFFAOYSA-N 4,5-dihydroxy-1,3-bis(hydroxymethyl)imidazolidin-2-one Chemical compound OCN1C(O)C(O)N(CO)C1=O ZEYUSQVGRCPBPG-UHFFFAOYSA-N 0.000 description 1
- XOJWAAUYNWGQAU-UHFFFAOYSA-N 4-(2-methylprop-2-enoyloxy)butyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCCOC(=O)C(C)=C XOJWAAUYNWGQAU-UHFFFAOYSA-N 0.000 description 1
- DBCAQXHNJOFNGC-UHFFFAOYSA-N 4-bromo-1,1,1-trifluorobutane Chemical compound FC(F)(F)CCCBr DBCAQXHNJOFNGC-UHFFFAOYSA-N 0.000 description 1
- SAPGBCWOQLHKKZ-UHFFFAOYSA-N 6-(2-methylprop-2-enoyloxy)hexyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCCCCOC(=O)C(C)=C SAPGBCWOQLHKKZ-UHFFFAOYSA-N 0.000 description 1
- FIHBHSQYSYVZQE-UHFFFAOYSA-N 6-prop-2-enoyloxyhexyl prop-2-enoate Chemical compound C=CC(=O)OCCCCCCOC(=O)C=C FIHBHSQYSYVZQE-UHFFFAOYSA-N 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 1
- 102100021971 Bcl-2-interacting killer Human genes 0.000 description 1
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 1
- 241000207199 Citrus Species 0.000 description 1
- 239000001116 FEMA 4028 Substances 0.000 description 1
- 101000970576 Homo sapiens Bcl-2-interacting killer Proteins 0.000 description 1
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- NQTADLQHYWFPDB-UHFFFAOYSA-N N-Hydroxysuccinimide Chemical class ON1C(=O)CCC1=O NQTADLQHYWFPDB-UHFFFAOYSA-N 0.000 description 1
- CNCOEDDPFOAUMB-UHFFFAOYSA-N N-Methylolacrylamide Chemical compound OCNC(=O)C=C CNCOEDDPFOAUMB-UHFFFAOYSA-N 0.000 description 1
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 1
- OKKRPWIIYQTPQF-UHFFFAOYSA-N Trimethylolpropane trimethacrylate Chemical compound CC(=C)C(=O)OCC(CC)(COC(=O)C(C)=C)COC(=O)C(C)=C OKKRPWIIYQTPQF-UHFFFAOYSA-N 0.000 description 1
- 229920006322 acrylamide copolymer Polymers 0.000 description 1
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- 230000009471 action Effects 0.000 description 1
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- 150000001298 alcohols Chemical class 0.000 description 1
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- 125000005211 alkyl trimethyl ammonium group Chemical group 0.000 description 1
- NBZANZVJRKXVBH-GYDPHNCVSA-N alpha-Cryptoxanthin Natural products O[C@H]1CC(C)(C)C(/C=C/C(=C\C=C\C(=C/C=C/C=C(\C=C\C=C(/C=C/[C@H]2C(C)=CCCC2(C)C)\C)/C)\C)/C)=C(C)C1 NBZANZVJRKXVBH-GYDPHNCVSA-N 0.000 description 1
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- YAMHXTCMCPHKLN-UHFFFAOYSA-N imidazolidin-2-one Chemical compound O=C1NCCN1 YAMHXTCMCPHKLN-UHFFFAOYSA-N 0.000 description 1
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- CDOSHBSSFJOMGT-UHFFFAOYSA-N linalool Chemical compound CC(C)=CCCC(C)(O)C=C CDOSHBSSFJOMGT-UHFFFAOYSA-N 0.000 description 1
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- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
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- FBCQUCJYYPMKRO-UHFFFAOYSA-N prop-2-enyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC=C FBCQUCJYYPMKRO-UHFFFAOYSA-N 0.000 description 1
- 235000018102 proteins Nutrition 0.000 description 1
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- 125000004076 pyridyl group Chemical group 0.000 description 1
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- JJMIAJGBZGZNHA-UHFFFAOYSA-N sodium;styrene Chemical compound [Na].C=CC1=CC=CC=C1 JJMIAJGBZGZNHA-UHFFFAOYSA-N 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- YBBRCQOCSYXUOC-UHFFFAOYSA-N sulfuryl dichloride Chemical class ClS(Cl)(=O)=O YBBRCQOCSYXUOC-UHFFFAOYSA-N 0.000 description 1
- 230000034005 thiol-disulfide exchange Effects 0.000 description 1
- 229940098465 tincture Drugs 0.000 description 1
- 238000005292 vacuum distillation Methods 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J13/00—Colloid chemistry, e.g. the production of colloidal materials or their solutions, not otherwise provided for; Making microcapsules or microballoons
- B01J13/02—Making microcapsules or microballoons
- B01J13/04—Making microcapsules or microballoons by physical processes, e.g. drying, spraying
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J13/00—Colloid chemistry, e.g. the production of colloidal materials or their solutions, not otherwise provided for; Making microcapsules or microballoons
- B01J13/02—Making microcapsules or microballoons
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
- C11D17/0039—Coated compositions or coated components in the compositions, (micro)capsules
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M23/00—Treatment of fibres, threads, yarns, fabrics or fibrous goods made from such materials, characterised by the process
- D06M23/12—Processes in which the treating agent is incorporated in microcapsules
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B82—NANOTECHNOLOGY
- B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
- B82Y30/00—Nanotechnology for materials or surface science, e.g. nanocomposites
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M2400/00—Specific information on the treatment or the process itself not provided in D06M23/00-D06M23/18
- D06M2400/01—Creating covalent bondings between the treating agent and the fibre
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2982—Particulate matter [e.g., sphere, flake, etc.]
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2982—Particulate matter [e.g., sphere, flake, etc.]
- Y10T428/2984—Microcapsule with fluid core [includes liposome]
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2982—Particulate matter [e.g., sphere, flake, etc.]
- Y10T428/2984—Microcapsule with fluid core [includes liposome]
- Y10T428/2985—Solid-walled microcapsule from synthetic polymer
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2982—Particulate matter [e.g., sphere, flake, etc.]
- Y10T428/2989—Microcapsule with solid core [includes liposome]
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2982—Particulate matter [e.g., sphere, flake, etc.]
- Y10T428/2991—Coated
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Dispersion Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Textile Engineering (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Chemical Or Physical Treatment Of Fibers (AREA)
- Fats And Perfumes (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP05111412 | 2005-11-29 | ||
| EP05111412.2 | 2005-11-29 | ||
| PCT/EP2006/068664 WO2007063001A1 (en) | 2005-11-29 | 2006-11-20 | Capsules |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BRPI0619196A2 true BRPI0619196A2 (pt) | 2011-09-20 |
Family
ID=36127283
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BRPI0619196-7A BRPI0619196A2 (pt) | 2005-11-29 | 2006-11-20 | cápsulas |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US8747999B2 (enExample) |
| EP (1) | EP1954795B8 (enExample) |
| JP (1) | JP5209487B2 (enExample) |
| KR (1) | KR101366569B1 (enExample) |
| CN (1) | CN101316924B (enExample) |
| AU (1) | AU2006319236B2 (enExample) |
| BR (1) | BRPI0619196A2 (enExample) |
| DE (1) | DE602006007875D1 (enExample) |
| TW (1) | TWI424109B (enExample) |
| WO (1) | WO2007063001A1 (enExample) |
Families Citing this family (32)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PT103265B (pt) * | 2005-04-22 | 2007-02-28 | Univ Do Minho | Microcápsulas com grupos funcionais reactivos de ligação a fibras têxteis e processo de aplicação e fixação |
| GB0623748D0 (en) * | 2006-11-28 | 2007-01-10 | Ciba Sc Holding Ag | Microcapsules, their use and processes for their manufacture |
| CA2734294A1 (fr) * | 2008-08-13 | 2010-02-18 | Long Lasting Innovation - L2I (Societe A Responsabilite Limitee) | Procede pour la fixation de molecules actives sur un support, element actif obtenu par ce procede et composition chimique pour la mise en oeuvre de ce procede |
| US8816023B2 (en) | 2008-08-13 | 2014-08-26 | Ppg Industries Ohio, Inc | Lightweight particles and compositions containing them |
| CN101461359B (zh) * | 2009-01-15 | 2012-07-04 | 中国农业大学 | 一种制备控释型纳米级农药的方法 |
| KR101356265B1 (ko) * | 2009-04-17 | 2014-02-06 | 바스프 에스이 | 방향제를 위한 캐리어 시스템 |
| GB0909909D0 (en) | 2009-06-09 | 2009-07-22 | Chrisal Nv | Microcapsules containing microrgnisms |
| AR083328A1 (es) * | 2010-07-20 | 2013-02-21 | Procter & Gamble | Particula de suministro |
| DE102010062286A1 (de) * | 2010-12-01 | 2012-06-06 | Rudolf Gmbh | Polykationische Kolloidpartikel, Verfahren zu deren Herstellung und deren Verwendung zur Modifizierung von Substraten |
| US9241513B2 (en) * | 2011-08-26 | 2016-01-26 | The Hong Kong Polytechnic University | Item of clothing for daily pharmacological treatment of a fungal infection |
| CN103987827A (zh) * | 2011-12-16 | 2014-08-13 | 荷兰联合利华有限公司 | 织物处理 |
| US20130340885A1 (en) * | 2012-06-22 | 2013-12-26 | Chromatic Technologies, Inc. | Thermochromic Level Indicator |
| US9809004B2 (en) * | 2014-07-18 | 2017-11-07 | E I Du Pont De Nemours And Company | Breathable protective apparel |
| CN104313765A (zh) * | 2014-11-04 | 2015-01-28 | 常熟市新达纬编厂 | 一种抗紫外线面料 |
| CN104404774B (zh) * | 2014-12-16 | 2016-10-05 | 江南大学 | 一种基于层层静电自组装的微胶囊多功能整理剂合成和应用工艺 |
| US9656233B2 (en) * | 2015-01-16 | 2017-05-23 | Encapsys, Llc | Reversible microcapsule filter cake |
| US10405541B2 (en) | 2015-04-22 | 2019-09-10 | International Business Machines Corporation | Encapsulated payloads bonded to polymeric materials |
| JP6659016B2 (ja) * | 2015-10-23 | 2020-03-04 | 花王株式会社 | マイクロカプセル |
| US9902799B2 (en) | 2015-11-11 | 2018-02-27 | Prc-Desoto International, Inc. | Urethane-modified prepolymers containing pendent alkyl groups, compositions and uses thereof |
| WO2017192407A1 (en) | 2016-05-02 | 2017-11-09 | Roman Bielski | Microcapsules for controlled delivery of an active pharmaceutical ingredient |
| KR101852870B1 (ko) * | 2016-07-22 | 2018-06-11 | 다이텍연구원 | 나노 / 마이크로캡슐이 혼입된 코스메틱 섬유 및 그 가공 방법 |
| JP6986571B2 (ja) | 2017-01-24 | 2021-12-22 | アグファ・ナームローゼ・フェンノートシャップAgfa Nv | カチオン分散基により安定化されたカプセル |
| US10280348B2 (en) | 2017-01-31 | 2019-05-07 | Prc-Desoto International, Inc. | Low density aerospace compositions and sealants |
| CN107374981B (zh) * | 2017-06-09 | 2020-07-07 | 雅弗生物实验室有限公司(加拿大) | 一种面/眼膜基材及其制备方法 |
| EP3587467A1 (de) | 2018-06-25 | 2020-01-01 | Rudolf GmbH | Funktionelle mehrwandige kern-schale-partikel |
| MX2021009603A (es) | 2019-02-11 | 2021-10-26 | Ppg Ind Ohio Inc | Impresion tridimensional de tapas de sellado. |
| DE102019107633A1 (de) | 2019-03-25 | 2020-10-29 | Sphera Technology Gmbh | Mehrkomponentensystem und Verfahren zur Herstellung eines Mehrkomponentensystems |
| US20230090216A1 (en) * | 2020-01-29 | 2023-03-23 | Huntsman Advanced Materials Switzerland Gmbh | Functionalized particles |
| DE102020124955B4 (de) | 2020-09-24 | 2025-04-03 | Cosa Group Gmbh | Elektronikeinheit mit einem integrierten Schaltkreis und Verfahren zu deren Herstellung |
| CN112898811B (zh) * | 2021-02-02 | 2022-07-19 | 三棵树(上海)新材料研究有限公司 | 一种抗菌自修复微胶囊及其制备方法和在涂料中的应用 |
| JP7672848B2 (ja) | 2021-03-16 | 2025-05-08 | 花王株式会社 | 繊維製品処理剤組成物 |
| CN113338030A (zh) * | 2021-06-08 | 2021-09-03 | 东华大学 | 一种基于纳米胶囊原位固化技术的芳香纺织品及其制备方法 |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB9110408D0 (en) * | 1989-08-24 | 1991-07-03 | Allied Colloids Ltd | Polymeric compositions |
| AU730956B2 (en) * | 1996-12-23 | 2001-03-22 | Ciba Specialty Chemicals Water Treatments Limited | Particles containing absorbed liquids and methods of making them |
| DE19932144A1 (de) * | 1999-07-09 | 2001-01-11 | Basf Ag | Mikrokapselzubereitungen und Mikrokapseln enthaltende Wasch- und Reinigungsmittel |
| AU2001246459A1 (en) * | 2000-02-23 | 2001-09-03 | Henkel Kommanditgesellschaft Auf Aktien | Microcapsules and/or nanocapsules |
| DE10027634A1 (de) * | 2000-06-06 | 2001-12-13 | Basf Ag | Verwendung von kationisch modifizierten, teilchenförmigen, hydrophoben Polymeren als Zusatz zu Spül- oder Pflegemitteln für Textilien und als Zusatz zu Waschmitteln |
| GB0029198D0 (en) * | 2000-11-30 | 2001-01-17 | Ciba Sc Holding Ag | Liquid dispersion polymer compositions their preparation and their use |
| GB0110989D0 (en) * | 2001-05-04 | 2001-06-27 | Polytek Hong Kong Ltd | Process of entrapping colorants |
| JP2003001100A (ja) * | 2001-06-04 | 2003-01-07 | Microcapsules Technologies | 陽イオン性マイクロカプセルを製造する方法 |
| GB0329129D0 (en) * | 2003-12-16 | 2004-01-21 | Unilever Plc | Laundry composition |
| EP1637188A1 (en) * | 2004-08-20 | 2006-03-22 | Firmenich Sa | Improved liquid/sprayable compositions comprising fragranced aminoplast capsules |
-
2006
- 2006-11-20 EP EP06819614A patent/EP1954795B8/en not_active Not-in-force
- 2006-11-20 WO PCT/EP2006/068664 patent/WO2007063001A1/en not_active Ceased
- 2006-11-20 CN CN2006800447767A patent/CN101316924B/zh not_active Expired - Fee Related
- 2006-11-20 BR BRPI0619196-7A patent/BRPI0619196A2/pt not_active IP Right Cessation
- 2006-11-20 DE DE602006007875T patent/DE602006007875D1/de active Active
- 2006-11-20 AU AU2006319236A patent/AU2006319236B2/en not_active Ceased
- 2006-11-20 KR KR1020087013402A patent/KR101366569B1/ko not_active Expired - Fee Related
- 2006-11-20 JP JP2008541720A patent/JP5209487B2/ja not_active Expired - Fee Related
- 2006-11-20 US US12/085,270 patent/US8747999B2/en not_active Expired - Fee Related
- 2006-11-27 TW TW095143672A patent/TWI424109B/zh not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| TW200806848A (en) | 2008-02-01 |
| EP1954795B8 (en) | 2009-08-26 |
| US8747999B2 (en) | 2014-06-10 |
| CN101316924B (zh) | 2012-01-11 |
| KR101366569B1 (ko) | 2014-03-14 |
| KR20080077616A (ko) | 2008-08-25 |
| CN101316924A (zh) | 2008-12-03 |
| JP2009517551A (ja) | 2009-04-30 |
| DE602006007875D1 (de) | 2009-08-27 |
| TWI424109B (zh) | 2014-01-21 |
| US20090155195A1 (en) | 2009-06-18 |
| EP1954795B1 (en) | 2009-07-15 |
| AU2006319236B2 (en) | 2012-07-19 |
| EP1954795A1 (en) | 2008-08-13 |
| AU2006319236A1 (en) | 2007-06-07 |
| WO2007063001A1 (en) | 2007-06-07 |
| JP5209487B2 (ja) | 2013-06-12 |
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Legal Events
| Date | Code | Title | Description |
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| B07A | Application suspended after technical examination (opinion) [chapter 7.1 patent gazette] | ||
| B08F | Application dismissed because of non-payment of annual fees [chapter 8.6 patent gazette] |
Free format text: REFERENTE A 10A ANUIDADE. |
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| B08K | Patent lapsed as no evidence of payment of the annual fee has been furnished to inpi [chapter 8.11 patent gazette] |
Free format text: EM VIRTUDE DO ARQUIVAMENTO PUBLICADO NA RPI 2386 DE 27-09-2016 E CONSIDERANDO AUSENCIA DE MANIFESTACAO DENTRO DOS PRAZOS LEGAIS, INFORMO QUE CABE SER MANTIDO O ARQUIVAMENTO DO PEDIDO DE PATENTE, CONFORME O DISPOSTO NO ARTIGO 12, DA RESOLUCAO 113/2013. |