WO2023111366A1 - Support pour parfum longue durée - Google Patents
Support pour parfum longue durée Download PDFInfo
- Publication number
- WO2023111366A1 WO2023111366A1 PCT/ES2021/070892 ES2021070892W WO2023111366A1 WO 2023111366 A1 WO2023111366 A1 WO 2023111366A1 ES 2021070892 W ES2021070892 W ES 2021070892W WO 2023111366 A1 WO2023111366 A1 WO 2023111366A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- fragrance
- support
- range
- excipient
- vinyl acetate
- Prior art date
Links
- 239000003205 fragrance Substances 0.000 title claims abstract description 209
- 230000005923 long-lasting effect Effects 0.000 title abstract description 4
- 239000000546 pharmaceutical excipient Substances 0.000 claims abstract description 56
- 239000005038 ethylene vinyl acetate Substances 0.000 claims abstract description 45
- -1 polyethylene Polymers 0.000 claims abstract description 42
- 239000004698 Polyethylene Substances 0.000 claims abstract description 40
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 claims abstract description 40
- 229920000573 polyethylene Polymers 0.000 claims abstract description 39
- 229920000642 polymer Polymers 0.000 claims abstract description 33
- 239000011159 matrix material Substances 0.000 claims abstract description 26
- SESFRYSPDFLNCH-UHFFFAOYSA-N benzyl benzoate Chemical compound C=1C=CC=CC=1C(=O)OCC1=CC=CC=C1 SESFRYSPDFLNCH-UHFFFAOYSA-N 0.000 claims abstract description 20
- 238000004806 packaging method and process Methods 0.000 claims abstract description 13
- 229960002903 benzyl benzoate Drugs 0.000 claims abstract description 10
- HIQIXEFWDLTDED-UHFFFAOYSA-N 4-hydroxy-1-piperidin-4-ylpyrrolidin-2-one Chemical compound O=C1CC(O)CN1C1CCNCC1 HIQIXEFWDLTDED-UHFFFAOYSA-N 0.000 claims abstract description 9
- 239000000203 mixture Substances 0.000 claims description 60
- 238000000034 method Methods 0.000 claims description 46
- 238000002347 injection Methods 0.000 claims description 22
- 239000007924 injection Substances 0.000 claims description 22
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims description 20
- 229920001577 copolymer Polymers 0.000 claims description 19
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 14
- 239000005977 Ethylene Substances 0.000 claims description 14
- 239000008240 homogeneous mixture Substances 0.000 claims description 11
- 239000007787 solid Substances 0.000 claims description 11
- 239000004753 textile Substances 0.000 claims description 9
- 235000020971 citrus fruits Nutrition 0.000 claims description 8
- 241000207199 Citrus Species 0.000 claims description 7
- 238000005470 impregnation Methods 0.000 claims description 7
- 229920001519 homopolymer Polymers 0.000 claims description 5
- 229920005638 polyethylene monopolymer Polymers 0.000 claims description 5
- 238000005507 spraying Methods 0.000 claims description 4
- 229920001903 high density polyethylene Polymers 0.000 claims description 3
- 239000004700 high-density polyethylene Substances 0.000 claims description 3
- 238000002156 mixing Methods 0.000 claims description 3
- NOOLISFMXDJSKH-UTLUCORTSA-N (+)-Neomenthol Chemical compound CC(C)[C@@H]1CC[C@@H](C)C[C@@H]1O NOOLISFMXDJSKH-UTLUCORTSA-N 0.000 claims description 2
- 235000001674 Agaricus brunnescens Nutrition 0.000 claims description 2
- 240000007154 Coffea arabica Species 0.000 claims description 2
- NOOLISFMXDJSKH-UHFFFAOYSA-N DL-menthol Natural products CC(C)C1CCC(C)CC1O NOOLISFMXDJSKH-UHFFFAOYSA-N 0.000 claims description 2
- 240000004760 Pimpinella anisum Species 0.000 claims description 2
- 235000012550 Pimpinella anisum Nutrition 0.000 claims description 2
- 244000299461 Theobroma cacao Species 0.000 claims description 2
- 235000009470 Theobroma cacao Nutrition 0.000 claims description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 2
- 235000016213 coffee Nutrition 0.000 claims description 2
- 235000013353 coffee beverage Nutrition 0.000 claims description 2
- 235000013365 dairy product Nutrition 0.000 claims description 2
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 claims description 2
- 229940041616 menthol Drugs 0.000 claims description 2
- 238000010298 pulverizing process Methods 0.000 claims description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 claims 1
- 229910052782 aluminium Inorganic materials 0.000 claims 1
- 229910052802 copper Inorganic materials 0.000 claims 1
- 239000010949 copper Substances 0.000 claims 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 claims 1
- 229910052737 gold Inorganic materials 0.000 claims 1
- 239000010931 gold Substances 0.000 claims 1
- 229910052759 nickel Inorganic materials 0.000 claims 1
- 229910052697 platinum Inorganic materials 0.000 claims 1
- 229910052709 silver Inorganic materials 0.000 claims 1
- 239000004332 silver Substances 0.000 claims 1
- 239000004744 fabric Substances 0.000 abstract description 4
- 238000013268 sustained release Methods 0.000 abstract description 4
- 239000012730 sustained-release form Substances 0.000 abstract description 4
- 238000013270 controlled release Methods 0.000 abstract description 3
- 238000004519 manufacturing process Methods 0.000 abstract 1
- DQXBYHZEEUGOBF-UHFFFAOYSA-N but-3-enoic acid;ethene Chemical compound C=C.OC(=O)CC=C DQXBYHZEEUGOBF-UHFFFAOYSA-N 0.000 description 25
- 239000000047 product Substances 0.000 description 9
- 239000000758 substrate Substances 0.000 description 9
- 239000000463 material Substances 0.000 description 7
- 239000002245 particle Substances 0.000 description 7
- 239000002304 perfume Substances 0.000 description 7
- 238000000113 differential scanning calorimetry Methods 0.000 description 6
- 230000000717 retained effect Effects 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 5
- ZFOZVQLOBQUTQQ-UHFFFAOYSA-N Tributyl citrate Chemical compound CCCCOC(=O)CC(O)(C(=O)OCCCC)CC(=O)OCCCC ZFOZVQLOBQUTQQ-UHFFFAOYSA-N 0.000 description 4
- 238000010521 absorption reaction Methods 0.000 description 4
- 238000002844 melting Methods 0.000 description 4
- 230000008018 melting Effects 0.000 description 4
- 230000002459 sustained effect Effects 0.000 description 4
- 229920001169 thermoplastic Polymers 0.000 description 4
- HDDLVZWGOPWKFW-UHFFFAOYSA-N trimethyl 2-hydroxypropane-1,2,3-tricarboxylate Chemical compound COC(=O)CC(O)(C(=O)OC)CC(=O)OC HDDLVZWGOPWKFW-UHFFFAOYSA-N 0.000 description 4
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 238000005899 aromatization reaction Methods 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 238000005538 encapsulation Methods 0.000 description 3
- 230000014759 maintenance of location Effects 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 239000008188 pellet Substances 0.000 description 3
- 239000004014 plasticizer Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- QZCLKYGREBVARF-UHFFFAOYSA-N Acetyl tributyl citrate Chemical compound CCCCOC(=O)CC(C(=O)OCCCC)(OC(C)=O)CC(=O)OCCCC QZCLKYGREBVARF-UHFFFAOYSA-N 0.000 description 2
- ZCTQGTTXIYCGGC-UHFFFAOYSA-N Benzyl salicylate Chemical compound OC1=CC=CC=C1C(=O)OCC1=CC=CC=C1 ZCTQGTTXIYCGGC-UHFFFAOYSA-N 0.000 description 2
- 239000004804 Butyryltrihexylcitrate Substances 0.000 description 2
- 235000005979 Citrus limon Nutrition 0.000 description 2
- 244000131522 Citrus pyriformis Species 0.000 description 2
- 241000675108 Citrus tangerina Species 0.000 description 2
- 240000000560 Citrus x paradisi Species 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- 244000179970 Monarda didyma Species 0.000 description 2
- 235000010672 Monarda didyma Nutrition 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- 239000004793 Polystyrene Substances 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- DOOTYTYQINUNNV-UHFFFAOYSA-N Triethyl citrate Chemical compound CCOC(=O)CC(O)(C(=O)OCC)CC(=O)OCC DOOTYTYQINUNNV-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 239000011111 cardboard Substances 0.000 description 2
- 238000009792 diffusion process Methods 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- HNMCSUXJLGGQFO-UHFFFAOYSA-N hexaaluminum;hexasodium;tetrathietane;hexasilicate Chemical compound [Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].S1SSS1.S1SSS1.[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-] HNMCSUXJLGGQFO-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 229920002223 polystyrene Polymers 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 230000002035 prolonged effect Effects 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 238000003892 spreading Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000004416 thermosoftening plastic Substances 0.000 description 2
- WEAPVABOECTMGR-UHFFFAOYSA-N triethyl 2-acetyloxypropane-1,2,3-tricarboxylate Chemical compound CCOC(=O)CC(C(=O)OCC)(OC(C)=O)CC(=O)OCC WEAPVABOECTMGR-UHFFFAOYSA-N 0.000 description 2
- 239000001069 triethyl citrate Substances 0.000 description 2
- VMYFZRTXGLUXMZ-UHFFFAOYSA-N triethyl citrate Natural products CCOC(=O)C(O)(C(=O)OCC)C(=O)OCC VMYFZRTXGLUXMZ-UHFFFAOYSA-N 0.000 description 2
- 235000013769 triethyl citrate Nutrition 0.000 description 2
- TUUQISRYLMFKOG-UHFFFAOYSA-N trihexyl 2-acetyloxypropane-1,2,3-tricarboxylate Chemical compound CCCCCCOC(=O)CC(C(=O)OCCCCCC)(OC(C)=O)CC(=O)OCCCCCC TUUQISRYLMFKOG-UHFFFAOYSA-N 0.000 description 2
- GWVUTNGDMGTPFE-UHFFFAOYSA-N trihexyl 2-butanoyloxypropane-1,2,3-tricarboxylate Chemical compound CCCCCCOC(=O)CC(C(=O)OCCCCCC)(OC(=O)CCC)CC(=O)OCCCCCC GWVUTNGDMGTPFE-UHFFFAOYSA-N 0.000 description 2
- APVVRLGIFCYZHJ-UHFFFAOYSA-N trioctyl 2-hydroxypropane-1,2,3-tricarboxylate Chemical compound CCCCCCCCOC(=O)CC(O)(C(=O)OCCCCCCCC)CC(=O)OCCCCCCCC APVVRLGIFCYZHJ-UHFFFAOYSA-N 0.000 description 2
- 239000000341 volatile oil Substances 0.000 description 2
- BSXJTDJJVULBTQ-UHFFFAOYSA-N 2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9,9-heptadecafluorononan-1-ol Chemical compound OCC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F BSXJTDJJVULBTQ-UHFFFAOYSA-N 0.000 description 1
- YISKDBXJCGZLEP-UHFFFAOYSA-N 9-acetyl-10-hydroxy-11-octylnonadecane-8,9,10-tricarboxylic acid Chemical compound CCCCCCCCC(CCCCCCCC)(C(O)=O)C(O)(C(O)=O)C(CCCCCCCC)(C(C)=O)C(O)=O YISKDBXJCGZLEP-UHFFFAOYSA-N 0.000 description 1
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- 241000951471 Citrus junos Species 0.000 description 1
- 240000007108 Fuchsia magellanica Species 0.000 description 1
- 235000010254 Jasminum officinale Nutrition 0.000 description 1
- 240000005385 Jasminum sambac Species 0.000 description 1
- 235000007265 Myrrhis odorata Nutrition 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 241000220317 Rosa Species 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- 240000006909 Tilia x europaea Species 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- IRERQBUNZFJFGC-UHFFFAOYSA-L azure blue Chemical compound [Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[S-]S[S-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-] IRERQBUNZFJFGC-UHFFFAOYSA-L 0.000 description 1
- IKZZIQXKLWDPCD-UHFFFAOYSA-N but-1-en-2-ol Chemical compound CCC(O)=C IKZZIQXKLWDPCD-UHFFFAOYSA-N 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 239000003610 charcoal Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000000806 elastomer Substances 0.000 description 1
- 239000008393 encapsulating agent Substances 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 239000000796 flavoring agent Substances 0.000 description 1
- 235000019634 flavors Nutrition 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 239000008241 heterogeneous mixture Substances 0.000 description 1
- YOBAEOGBNPPUQV-UHFFFAOYSA-N iron;trihydrate Chemical compound O.O.O.[Fe].[Fe] YOBAEOGBNPPUQV-UHFFFAOYSA-N 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 238000011068 loading method Methods 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 229920001684 low density polyethylene Polymers 0.000 description 1
- 239000004702 low-density polyethylene Substances 0.000 description 1
- 230000000873 masking effect Effects 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 230000009965 odorless effect Effects 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 239000012255 powdered metal Substances 0.000 description 1
- 238000012797 qualification Methods 0.000 description 1
- 230000001953 sensory effect Effects 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- UJMBCXLDXJUMFB-UHFFFAOYSA-K trisodium;5-oxo-1-(4-sulfonatophenyl)-4-[(4-sulfonatophenyl)diazenyl]-4h-pyrazole-3-carboxylate Chemical compound [Na+].[Na+].[Na+].[O-]C(=O)C1=NN(C=2C=CC(=CC=2)S([O-])(=O)=O)C(=O)C1N=NC1=CC=C(S([O-])(=O)=O)C=C1 UJMBCXLDXJUMFB-UHFFFAOYSA-K 0.000 description 1
- 235000013799 ultramarine blue Nutrition 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 239000012855 volatile organic compound Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000003643 water by type Substances 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/04—Homopolymers or copolymers of ethene
- C08L23/08—Copolymers of ethene
- C08L23/0846—Copolymers of ethene with unsaturated hydrocarbons containing other atoms than carbon or hydrogen atoms
- C08L23/0853—Vinylacetate
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L9/00—Disinfection, sterilisation or deodorisation of air
- A61L9/015—Disinfection, sterilisation or deodorisation of air using gaseous or vaporous substances, e.g. ozone
- A61L9/04—Disinfection, sterilisation or deodorisation of air using gaseous or vaporous substances, e.g. ozone using substances evaporated in the air without heating
- A61L9/042—Disinfection, sterilisation or deodorisation of air using gaseous or vaporous substances, e.g. ozone using substances evaporated in the air without heating with the help of a macromolecular compound as a carrier or diluent
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L9/00—Disinfection, sterilisation or deodorisation of air
- A61L9/01—Deodorant compositions
- A61L9/013—Deodorant compositions containing animal or plant extracts, or vegetable material
Definitions
- fragrance diffusion can be enhanced, for example, by heating the fragrance, including the fragrance in a volatile carrier, by the use of membranes, or by a combination thereof.
- the diffusion of fragrances and their overall intensity is governed by their equilibrium vapor pressure. Fragrances with a high equilibrium vapor pressure have high volatility and evaporate quickly.
- the useful life of a fragrance device is limited by the amount of fragrance that can be dispensed from the device.
- one of the difficulties in selecting a carrier that allows uniform fragrance distribution at a selected rate is that some carriers and fragrances evaporate too quickly or conversely too slowly and/or insufficiently to create the desired fragrance. , in a large room.
- Controlled release of fragrances may traditionally require pre-packaging of encapsulated fragrances in the final product.
- encapsulation can be functional, sometimes encapsulation can lead to unbalanced fragrance release profiles, due to chemical incompatibility of the fragrance with the encapsulating agents or maldistribution of the fragrance in the encapsulated particles or substances.
- encapsulation is expensive and therefore increases the cost of the underlying product.
- US4515909 is one of the first documents to describe a fragrance article comprising polymeric substrates.
- Said article comprises an ethylene-vinyl acetate (EVA) copolymer impregnated with a diffusing agent and a fragrance, wherein said copolymer contains between 15% to 30% of the vinyl acetate monomer, by weight, and about 85% to 70% ethylene monomer, by weight.
- EVA ethylene-vinyl acetate
- the spreading agent that can be used in said article is selected from the group consisting of benzyl benzoate, benzyl salicylate and mixtures thereof, said spreading agent being absorbed in the EVA copolymer in an amount by weight of approximately 1% up to the 10%.
- the patent, US4515909 also describes a method for preparing this fragrance article that first comprises mixing the EVA copolymer and the diffusing agent for a time interval between 1 to 5 hours at a temperature range between 50-76 °C, until that said diffusing agent is completely absorbed by the copolymer. Subsequently, the generated impregnated copolymer can be obtained in the form of a pellet and this is placed in contact with the fragrance at room temperature until the fragrance is absorbed by the previously impregnated copolymer (pellet).
- the impregnated pellets can also be molded in various shapes, such as EVA sheets with dimensions 1 cm x 1.5 cm x 0.3 cm, to be subsequently impregnated with a specific fragrance until each sheet has absorbed 30%. by weight of said fragrance, for a period of at least two hours.
- EP 1479757B1 describes a method for imparting to fabrics that are washed in a washing machine for one or more wash cycles and/or to fabrics that are dried in a tumble dryer for one or more drying cycles. , a fragrance with long-lasting unsightly properties.
- EP1479757B1 describes a method for imparting said fragrance using a hollow bag/envelope/package inside that comprises multiple solid or viscoelastic particles with a total weight of 2 g to 50 g, each particle having an average effective diameter. from 0.5mm-10mm.
- Said unblown polymeric particles for fragrances consist of a solid/viscous porous particle comprising, by weight, EVA (30%) with a ratio of ethylene:vinyl acetate units of 60:40, PE low density (50%) and a fragrance (20%).
- strips or transparent tapes with a thickness between 1-200 thousandths of an inch (0.025-5 mm), which comprise a substrate that contains at least one copolymer of a define, at least one derivative of a define and a fragrance, wherein said substrate is substantially free of homopolymeric material, said homopolymeric material being, for example, polystyrene, polyethylene, polypropylene or other homopolymers known in the state of the art.
- the copolymer is selected from the group consisting of ethylene-vinyl acetate, propylene-vinyl acetate, and a mixture thereof, and the define derivative is selected from saturated carboxylic acid vinyl esters, saturated carboxylic acid propenyl esters , olefinically unsaturated organic acids and esters, and mixtures thereof.
- the method of preparing these substrates in the form of strips or tapes that is carried out by means of the homogeneous mixture of the copolymer, the perfume, a suitable solvent (such as toluene), and optionally an adjuvant.
- the obtained mixture is then deposited by casting or coating on a silicone release liner, followed by drying at an elevated temperature to remove the solvent. After drying, the strip or tape can be retained in the release liner, or removed from the release liner for use in the applications described herein.
- WO 2008/153680 A has the disadvantage that it requires the use of organic solvents to be able to apply the perfume to the substrate, followed by the application of high temperatures for their evaporation.
- This fragrance dispensing device comprises an electrical resistance, plug or other power source and fragrance in a thermoplastic polymer or carrier.
- the thermoplastic polymer or carrier also has metal inclusions, such as powdered metal.
- the thermoplastic carrier is selected from the group consisting of ethylene vinyl acetate (EVA), ethyl vinyl alcohol, high density polyethylene, low density polyethylene, polystyrene, acrylic polymers, polycarbonates, polyurethanes, nylons, blends and copolymers of the foregoing.
- fragrance articles that are easy to hold or handle by hand, that can provide controlled and sustained release over time, as well as sufficient to create the desired fragrance in a large room or enclosed space, in containers or containers, would be desirable.
- the first aspect of the invention is related to a fragrance support comprising at least:
- an excipient where the excipient is selected from the list consisting of benzyl benzoate and isopropyl myristate; where the fragrance is impregnated in the polymeric matrix and where the excipient is present in the fragrance support in a weight range from 1-35%, preferably between 2-30%.
- the good compatibility of the excipients with the polymeric matrix helps to retain and/or absorb the fragrance in the polymeric matrix, which facilitates a prolonged release of the fragrance over time. Likewise, it facilitates the release of the fragrance both during transport and during its use in open rooms and releases fragrances of a different nature in a sustained manner, such as citrus, floral, wild or marine fragrances.
- the support of the first aspect of the invention does not comprise an electrical resistance, a plug or another power source.
- the term "fragrance carrier” comprises a compact solid that has no voids or spaces.
- the fragrance support does not comprise any envelope or bag having an interior compartment.
- the fragrance support is a compact solid that can be spherical, tablet or rectangular in shape.
- the fragrance support is a compact solid in the shape of a sphere, the 3 dimensions that define it will have the same width or diameter (1) with a range between 1.5 and 15 cm or is a compact tablet-shaped or rectangular-shaped solid, where said support can have a width or diameter (1) within a range between 1.5 and 15 cm and/or a height (2) within a range between 0.5 up to 3 cm and/or a depth (3) in a range between 2-15 cm.
- the width or diameter (1) is measured taking the ends furthest from the center of the tablet as a reference point, as indicated in figures 1-3. Said dimensions facilitate its handling and that it can be used both in large spaces and in small-sized containers or packaging.
- the dimensions of the previous embodiment make it possible to obtain a light support that is easy to transport and to incorporate into different types of packaging, such as envelopes, boxes, bags, cardboard tubes, or any package or container that may be included in its inside the support of the first aspect.
- the packaging, containers or containers can be selected from the list consisting of cardboard, plastic, crystal, glass or metal.
- polymeric matrix or substrate includes a primary phase that comprises a material composed of at least two polymers in which a secondary phase is embedded that can comprise fragrances, excipients, solid particles, liquids, or gels.
- a secondary phase is embedded that can comprise fragrances, excipients, solid particles, liquids, or gels.
- the polymeric components of the primary phase must not completely dissolve or fuse with each other, they must be physically identifiable as they form a heterogeneous mixture.
- the terms polymer matrix or substrate can be used interchangeably.
- Fragrance holder has the advantages that it can release a wide range of fragrances over a long period of time in a sustained manner.
- the support for fragrance of the first aspect can sustainably retain and release fragrances of different natures such as citrus, floral, wild or marine fragrances, while it can comprise a concentration by weight of each of them, to ensure long duration. both during transport and during use in open rooms.
- Fragrance support also has the advantage that it can release fragrance in a controlled manner at a rate that is adequate for human sensory satisfaction and/or malodour masking.
- the second aspect of the invention is related to a process for obtaining the fragrance support according to the first aspect of the invention, which comprises at least the following stages: a) the ethylene-vinyl acetate copolymer is impregnated with a mixture that it comprises a fragrance and an excipient, at a temperature in a range from 10 to 90 °C; b) the product obtained in the previous stage is mixed with polyethylene until a homogeneous mixture is obtained in a temperature range from 40 to 80 °C; c) the mixture obtained in the previous stage is injected inside an injection mould; d) is removed from the fragrance support of the finished mould, after completion of step c) of the injection mould.
- the process of the second aspect allows the ethylene-vinyl acetate (EVA) copolymer to be impregnated with the fragrance and the excipient in a single stage, reducing process times while allowing the correct impregnation and absorption of both in the EVA and the matrix of the support so that the fragrances are retained and are subsequently released in a sustained manner over time for a long period of time.
- EVA ethylene-vinyl acetate
- the third aspect of the invention is related to the support obtainable through the process of the second aspect.
- the fourth aspect of the invention is related to the use of the support for fragrance of the first aspect and of the fragrance obtainable through the process of the second aspect, in the aromatization of commercial premises, clothing, textile, furniture or merchandise stores, as well as to flavor containers, containers or packaging adapted to be closed suitable for clothing, textiles, pieces, decorative objects or furniture.
- Figure 1 3-dimensional representation of a particular embodiment of the support for fragrances with a spherical shape.
- Figure 2 Representation in 3 dimensions of a particular embodiment of the tablet-shaped support for fragrances.
- Figure 3 Representation in 3 dimensions of a particular embodiment of the support for fragrances with a rectangular shape.
- the first aspect of the invention is related to a fragrance support comprising at least: (i) a polymer matrix containing;
- an excipient where the excipient is selected from the list consisting of benzyl benzoate and isopropyl myristate; where the fragrance is impregnated in the polymer matrix and where the excipient is present in the fragrance support in a weight range from 1-35%, preferably between 2-30%
- the polymeric matrix does not contain metals in the form of aluminum powder.
- the fragrance is impregnated and/or retained in the polymeric matrix, preferably the fragrance is impregnated and/or retained in the EVA comprised in the polymeric matrix.
- the excipient is selected from the list consisting of benzyl benzoate, isopropyl myristate and mixtures thereof, where the mixtures thereof comprise benzyl benzoate and isopropyl myristate in a Weight ratio from 80/20 to 20/80.
- fragrance and the excipient are retained in the polymeric matrix.
- the fragrance carrier further comprises one or more additives.
- the additives can be selected from plasticizers, diluents and/or colorants.
- the additive is a dye selected from the list consisting of, Yellow Oxide (Cl 77492), Red Oxide (Cl 77491), Green Oxide (Cl 77288), Ultramarine Blue (Cl 77007), Ultramarine Pink (Cl 77007), Ultramarine Violet (Cl 77007), Titanium Dioxide (Cl 77891), Zinc Oxide (Cl 77949), Black Oxide (Cl 77499), Charcoal (Cl 77268), Tartrazine Yellow (Cl 19140), Egg Yellow ( Cl.
- Plasticizers can also be added to polymeric materials that are used in embodiments of the invention.
- Plasticizers can be selected from a list consisting of; Bis(n-butyl)phthalate, polyethylene glycol with molecular weight (Mn) ranging from 200-6000, Triethylcitrate (TEC), Acetyltriethylcitrate (ATEC), Tributylcitrate (TBC), Acetyltributylcitrate (ATBC), Trioctylcitrate (TOC), Acetyltrioctylcitrate ( ATOC),
- Trihexylcitrate THC
- Acetyltrihexylcitrate HAC
- Butyryltrihexylcitrate BTHC, trihexyl o-butyrylcitrate
- Trimethylcitrate TMC
- tricetic acid ester of glycerin and citric acid THC
- the polymeric matrix is present in the fragrance carrier in a percentage by weight from 45-92%, more preferably in a percentage by weight from 50-90%.
- polyethylene polymer includes polyethylene homopolymers and polyethylene copolymers having a density from 945-980 kg/m 3 , preferably from 950-975 kg/m 3 and/or a point of melting point measured by DSC between 120-150 °C, preferably melting point measured by DSC (differential scanning calorimetry) is between 125-140 °C.
- the DSC measurement was carried out with a heating rate of 10 degrees per minute.
- the polyethylene copolymers can be copolymers of polyethylene and polypropylene.
- the polyethylene polymer used in the invention can have a hardness, measured with a durometer according to the ISO 868 method on the D scale, in a range between 75-90, preferably between 63-72.
- the polyethylene polymer is a polyethylene homopolymer. In another more preferred embodiment the polyethylene polymer consists of a polyethylene homopolymer. In another even more preferred embodiment, the polyethylene polymer is a high density polyethylene homopolymer.
- polyethylene is present in the fragrance carrier in a percentage by weight from 3-25%, more preferably in a percentage by weight from 5-20%.
- the fragrance carrier of the first aspect has good fragrance retention and release despite its high polyethylene content.
- EVA Ethylene vinyl acetate copolymers
- EVA ethylene vinyl acetate copolymer and (EVA) comprises between 20-40% by weight of vinyl acetate and/or between 80-60% by weight of ethylene.
- EVA used in the invention can have a hardness measured with a durometer according to the ASTM D 2240 method, on the A scale, in a range between 75-90, preferably between 78-85.
- the supports that comprise a copolymer of ethylene and vinyl acetate comprise vinyl acetate in a range between 20-40% by weight and/or ethylene in a range between 80-60% by weight. of provide better fragrance release over a long period of time without the need to use an electrical resistance, a plug or another power source.
- the EVA copolymer has a melting point, measured by DSC, in a range between 55-85 °C, preferably between 60-80 °C. Melting point measurement by DSC was carried out at a temperature rise rate of 10 C/min.
- the EVA copolymer has a density measured by the ASTM D 1505 method, in a range between 0.92-0.98 g/cm 3 .
- the EVA is present on the fragrance carrier in a percentage by weight from 25-80%, more preferably in a percentage by weight from 30-75%.
- fragrance comprises, fragrances or fragrance compositions, fragrances based on water or natural oils, which may be volatile and may be transmitted to the olfactory system.
- fragrance and perfume can mean one or more different fragrance molecules as mixtures or blends of fragrance molecules.
- fragrance can include one or more aromatic properties, such as fragrance materials such as top fragrance, mid fragrance, or base fragrance; these fragrances or their compositions are often used, such as including but not limited to essential oils, aromatic essential oils, various scents, fragrance family floral, citrus fragrance family, marine fragrance family and/or wild and floral fragrance family.
- suitable fragrances include, but are not limited to Smoky, Aldehyde, Aliaceous, Musky, Woody, Animal, Anise, Powdery, Balsamic/Menthol, Cocoa, Coffee, Coniferous, Leather, Sweet, Spicy, Fruity, Gourmande, Mushroom/Earthy, Dairy, Marine/Ozonic, Oriental, Earthy, Toasty, Green, Vinous
- fragrance is preferably in liquid or oil form.
- the floral family of fragrances is one of the most popular and extensive of all perfume families. This family includes all the perfumes whose main theme is the olfactory representation of a single flower (soliflore) or a set of vandalized flowers (bouquet). Enriching them with accessory notes, they give rise to subgroups such as green floral, aquatic, fruity, white flower, floral-aldehyde, spicy and floriental fragrances. The most classic and iconic floral notes are three: rose, jasmine and neroli.
- the family of citrus fragrances also known as Hes Southernde, is characterized by being eminently composed of top notes from citrus fruit peels such as bergamot, lemon, orange, tangerine or grapefruit. They are usually soft and fresh fragrances, with an acid touch. Probably the most iconic fragrances that can be included in this family are the traditional cologne waters, made up of fresh and volatile notes, the common notes in this type of perfume are; lemon, orange, lime, grapefruit, bergamot, tangerine, yuzu, petitgrain, neroli, orange blossom.
- the fragrance is present in the fragrance carrier in a range between 3-25% by weight.
- the second aspect of the invention is related to a process for obtaining the fragrance support according to the first aspect of the invention, which comprises at least the following stages: a) the ethylene-vinyl acetate copolymer is impregnated with a mixture that it comprises a fragrance and an excipient, at a temperature in a range from 10 to 90 °C; preferably in a range from 20-80 °C; b) the mixture obtained in the previous stage is maintained in a temperature range between 10 to 90 °C; preferably in a range from 20-80 °C, for a period of time between 2-7 hours; c) the product obtained in the previous stage is mixed with polyethylene until a homogeneous mixture is obtained in a temperature range from 10 to 90 °C; preferably in a range from 20-80 °C; d) the mixture obtained in the previous stage is injected inside an injection mold at a temperature in a range between 110-140 °C; and e) is removed from the finished mold fragrance support, after completion of
- the ethylene vinyl acetate (EVA) copolymer of step a) of the second aspect of the invention corresponds to and is the same as the EVA copolymer of the first aspect of the invention.
- the polyethylene of step b) of the second aspect of the invention corresponds to and is the same as the polyethylene of the first aspect of the invention.
- the excipient and fragrance are mixed in an excipient/fragrance weight ratio in a range from 2.5-0.1, preferably in a range from 2-0.3, plus preferably in a range from 2-0.5.
- the impregnation step b) is carried out by spraying, pulverizing or spraying techniques.
- the mixing process of stage b) is carried out in a time range from 15 to 180 min, depending on the fragrance and the composition to be prepared. Preferably, between 15 min and 120 min.
- the ethylene vinyl acetate copolymer and the polyethylene polymer used are preferably in the form of a squawk.
- the mold has the dimensions of the fragrance holder.
- said process comprises at least the following stages: a) the ethylene-vinyl acetate copolymer is impregnated with a mixture comprising a fragrance and an excipient, a a temperature in a range from 10 to 90 °C; preferably in a range from 20-80 °C, where the excipient is selected from the list consisting of benzyl benzoate and isopropyl myristate; and where optionally weight ratio of ethylene vinyl acetate copolymer to excipient is from 20:1 to 1:1; b) the product obtained in the previous stage is mixed with a polyethylene polymer until a homogeneous mixture is obtained in a temperature range from 10 to 90 °C; preferably in a range from 20-80 °C; c) the product obtained in the previous stage is mixed with polyethylene until a homogeneous mixture is obtained in a temperature range from 10 to 90 °C; preferably in a range
- said process comprises at least the following stages: a) the ethylene-vinyl acetate copolymer is impregnated with a mixture comprising a fragrance and an excipient, a a temperature in a range from 10 to 90 °C; preferably in a range from 20-80 °C, where the excipient is selected from the list consisting of benzyl benzoate and isopropyl myristate; where the weight ratio of ethylene vinyl acetate copolymer to excipient is from 20:1 to 1:1 and where the mixture of fragrance and excipient comprises a weight concentration of the excipient in the mixture from 35% to 65% ; b) the product obtained in the previous stage is mixed with a polyethylene polymer until a homogeneous mixture is obtained in a temperature range from 10 to 90 °C; preferably in a range from 20-80 °C; c) the product obtained in the previous stage is mixed with polyethylene until
- said process comprises at least the following stages: a) the ethylene-vinyl acetate copolymer is impregnated with a mixture comprising a fragrance and an excipient, a a temperature in a range from 10 to 90 °C; preferably in a range from 20-80 °C; where the excipient is selected from the list consisting of benzyl benzoate and isopropyl myristate; where the weight ratio of the ethylene vinyl acetate copolymer to the mixture, fragrance and excipient, is from 8:1 to 0:4; and optionally where the mixture of fragrance and excipient comprises a weight concentration of the excipient in the mixture from 35% to 65%, b) the product obtained in the previous stage is mixed with a polyethylene polymer until a homogeneous mixture in a temperature range from 10 to 90 °C; preferably from 20-80 °C; c) the product obtained in the previous stage
- the weight ratio of the ethylene and vinyl acetate copolymer to the mixture, fragrance and excipient is from 8:1 to 0:4 and/or the fragrance and excipient mixture comprises a weight concentration of the excipient in the mixture from 35% to 65%.
- the fragrance is mixed with the excipient in the appropriate proportions as described in the first aspect of the invention.
- the EVA copolymer is impregnated with the newly obtained mixture of fragrance and excipient, for a time range from 15 min to 90 min in a mixer at a temperature in a range between 10-90 °C, preferably between 15-75°C.
- the polyethylene polymer is added to the same mixer, where they are mixed for a period of time between 15-60 min at a temperature in a range between 10-60 °C, preferably between 15-40 °C.
- the mixture obtained is injected into an injection mold that works at an injection temperature range between 110-140 °C.
- the fragrance support obtained has the advantage that it retains both the fragrance and the excipient once the last stages d) and e) have been completed, providing a fragrance support that allows the prolonged release of the fragrance over time for at least 1 month, more preferably for 2 months, without the need to heat the support or connect said support to any electrical device.
- the process of the second aspect allows the ethylene-vinyl acetate (EVA) copolymer to be impregnated with the fragrance and the excipient in a single stage, reducing process times while allowing the correct impregnation and absorption of both in the EVA and the matrix of the support so that they are retained and are released in a sustained manner over time for a long period of time. Preferably for at least 1 month, more preferably for at least 2 months, most preferably for at least 3 months.
- the correct impregnation and absorption, as well as its sustained release, are carried out even after the injection and extraction stages of the mold c) and d) respectively.
- Carrying out stage a) in which the impregnation of the EVA copolymer with the excipient and the fragrance is carried out in a single stage also facilitates the retention of the fragrance in the polymeric matrix during and after the injection process, obtaining shorter processes, reducing fragrance loss during injection, obtaining better retention and absorption of the fragrance and better release of the fragrance in the final fragrance support once the process is completed.
- the process of the second aspect allows the preparation of these supports with polyethylene polymers, which showed incompatibility, as indicated in the state of the art, in the preparation of articles, supports or substrates for fragrances.
- the third aspect of the invention is related to the support obtainable through the process of the second aspect.
- the fourth aspect of the invention is related to the use of the support for fragrance of the first aspect in the aromatization of commercial premises, clothing stores, textiles, furniture or merchandise, as well as to aromatize containers, containers or packaging adapted to be closed suitable for clothing, textiles, pieces, decorative objects or furniture.
- the support of the first aspect as well as the support obtained from the process of the second aspect, has the advantage that it does not leave residues on clothing, textiles, packaging or materials that are in its vicinity, therefore it does not cause deterioration to said items. materials or packaging.
- the fourth aspect of the invention is related to the use of the support for fragrance of the first aspect or the support for fragrance obtained from the second aspect in the aromatization of commercial premises, clothing, textiles, furniture or merchandise stores, as well as to aromatize containers, containers or packaging adapted to be closed, being these suitable for clothing, textiles, pieces, decorative objects or furniture.
- Example 1 support composition for fragrance comprising fragrance from the wild family.
- 1 % by weight refers to the total fragrance support.
- the wild fragrance is mixed with the excipient.
- the EVA copolymer is impregnated with the newly obtained mixture of fragrance and excipient, for 25 min in a mixer at a temperature in a range between 21-48 °C.
- the mixture is then kept at that temperature for 4 hours.
- the polyethylene polymer is added to the same mixer and this is mixed for 30 min at a temperature in a range between 21-48 °C.
- the mixture obtained is injected into an injection mold that works at a temperature range between 110-140 °C.
- the EVA used has a ratio of % VA (vinyl acetate) between 25-30%.
- Example 2 Support composition for fragrance comprising fragrance from the marine family.
- the Marina fragrance is mixed with the excipient.
- the EVA copolymer is impregnated with the newly obtained mixture of fragrance and excipient, for 25 min in a mixer at a temperature in a range between 21-55 °C, the mixture is maintained at that temperature for 4 hours.
- the polyethylene polymer is added to the same mixer and this is mixed for 30 min at a temperature in a range between 21-55 °C.
- the mixture obtained is injected into an injection mold that works at a temperature range between 110-140 °C.
- the EVA used has a ratio of % VA (vinyl acetate) between 25-30%.
- Example 3 Support composition for fragrance comprising fragrance from the citrus family.
- 1 % by weight refers to the total fragrance support.
- the citrus fragrance is mixed with the excipient.
- the EVA copolymer is impregnated with the newly obtained mixture of fragrance and excipient, for 25 min in a mixer at a temperature in a range between 21-35 °C and a stirring speed in a range from 200- 1000 rpm. The mixture is then kept at that temperature for 5 hours.
- the polyethylene polymer is added to the same mixer and this is mixed for 30 min at a temperature in a range between 21-35 °C.
- the mixture obtained is injected into an injection mold that works at a temperature range between 110-140 °C.
- the EVA used has a ratio of % VA (vinyl acetate) between 25-30%.
- Example 4 support composition for fragrance comprising fragrance of the floral family.
- 1 % by weight refers to the total fragrance support.
- the floral fragrance is mixed with the excipient.
- the EVA copolymer is impregnated with the newly obtained mixture of fragrance and excipient, for 25 min in a mixer at a temperature in a range between 21-70 °C. the mixture is then maintained at that temperature for 3.5 hours.
- the Polyethylene polymer is added to the same mixer and this mixture is mixed for 30 min at a temperature in a range between 21-70 °C.
- the mixture obtained is injected into an injection mold that works at a temperature range between 110-140 °C.
- the EVA used has a ratio of % VA (vinyl acetate) between 25-30%.
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Abstract
La présente invention se rapporte à un support pour parfum longue durée et le procédé d'obtention de ce dernier. Le support selon l'invention comprend au moins: i) une matrice polymère qui contient; - un copolymère d'éthylène et d'acétate de vinyle et - un polymère de polyéthylène; ii) un parfum; et iii) un excipient, lequel excipient est sélectionné dans la liste qui est constituée de benzoate de benzyle et de myristate d'isopropyle; lequel parfum est imprégné dans la matrice polymère et l'excipient est présent dans le support pour des parfums dans une plage en poids comprise entre 1 et 35%. Ledit support peut assurer une libération contrôlée et soutenue dans le temps, et peut créer le parfum désiré de manière suffisante dans une pièce de grande taille ou dans des lieux fermés, dans des contenants ou des récipients adaptés pour être fermés ou dans les différents types d'emballages pour le transport. La présente invention se rapporte également à l'utilisation dudit support pour parfumer des locaux commerciaux, des magasins de vêtements, de textiles, de meubles ou de marchandises, ainsi que pour parfumer des contenants, des récipients ou des emballages adaptés pour être fermés, étant donné qu'ils sont appropriés pour des vêtements, des textiles, des pièces, des objets de décoration ou des meubles.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
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PCT/ES2021/070892 WO2023111366A1 (fr) | 2021-12-15 | 2021-12-15 | Support pour parfum longue durée |
ES202490041A ES2977008A2 (es) | 2021-12-15 | 2021-12-15 | Soporte para fragancia de uso duradero |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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PCT/ES2021/070892 WO2023111366A1 (fr) | 2021-12-15 | 2021-12-15 | Support pour parfum longue durée |
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WO2023111366A1 true WO2023111366A1 (fr) | 2023-06-22 |
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PCT/ES2021/070892 WO2023111366A1 (fr) | 2021-12-15 | 2021-12-15 | Support pour parfum longue durée |
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WO (1) | WO2023111366A1 (fr) |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4515909A (en) | 1982-02-16 | 1985-05-07 | Kiyohito Sawano | Resinous composition for the prolonged release of fragrant substances |
EP1479757B1 (fr) | 2003-05-20 | 2008-01-02 | INTERNATIONAL FLAVORS & FRAGRANCES INC. | Methode conferant une fragrance substantive et optionnellement des proprietes anti-statiques aux textiles pendant la procedure de lavage et/ou de sechage |
US20080292509A1 (en) * | 2007-05-23 | 2008-11-27 | D Amico Daniel | Disposable Air Freshener Including Gel or Polymer Fragrance Support |
WO2008153680A1 (fr) | 2007-05-21 | 2008-12-18 | S. C. Johnson & Son, Inc. | Procedes de diffusion de parfum au moyen d'un 'ruban' d'acetate de vinyle-ethylene |
US20100254829A1 (en) * | 2009-04-01 | 2010-10-07 | Harris Neal F | Attachment to air moving device or system for the purpose of scenting spaces |
-
2021
- 2021-12-15 ES ES202490041A patent/ES2977008A2/es active Pending
- 2021-12-15 WO PCT/ES2021/070892 patent/WO2023111366A1/fr active Application Filing
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4515909A (en) | 1982-02-16 | 1985-05-07 | Kiyohito Sawano | Resinous composition for the prolonged release of fragrant substances |
EP1479757B1 (fr) | 2003-05-20 | 2008-01-02 | INTERNATIONAL FLAVORS & FRAGRANCES INC. | Methode conferant une fragrance substantive et optionnellement des proprietes anti-statiques aux textiles pendant la procedure de lavage et/ou de sechage |
WO2008153680A1 (fr) | 2007-05-21 | 2008-12-18 | S. C. Johnson & Son, Inc. | Procedes de diffusion de parfum au moyen d'un 'ruban' d'acetate de vinyle-ethylene |
US20080292509A1 (en) * | 2007-05-23 | 2008-11-27 | D Amico Daniel | Disposable Air Freshener Including Gel or Polymer Fragrance Support |
US8119072B2 (en) | 2007-05-23 | 2012-02-21 | Scent2Market Inc. | Disposable air freshener including gel or polymer fragrance support |
US20100254829A1 (en) * | 2009-04-01 | 2010-10-07 | Harris Neal F | Attachment to air moving device or system for the purpose of scenting spaces |
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