MXPA00001755A - Polymeric wick composition for air freshener candle product - Google Patents
Polymeric wick composition for air freshener candle productInfo
- Publication number
- MXPA00001755A MXPA00001755A MXPA/A/2000/001755A MXPA00001755A MXPA00001755A MX PA00001755 A MXPA00001755 A MX PA00001755A MX PA00001755 A MXPA00001755 A MX PA00001755A MX PA00001755 A MXPA00001755 A MX PA00001755A
- Authority
- MX
- Mexico
- Prior art keywords
- candle wick
- wick according
- candle
- ingredient
- air
- Prior art date
Links
- 239000002386 air freshener Substances 0.000 title claims abstract description 27
- 239000000203 mixture Substances 0.000 title abstract description 40
- 239000004615 ingredient Substances 0.000 claims abstract description 22
- -1 polyethylene Polymers 0.000 claims abstract description 19
- 239000000945 filler Substances 0.000 claims abstract description 9
- 239000004698 Polyethylene (PE) Substances 0.000 claims abstract description 5
- 229920000573 polyethylene Polymers 0.000 claims abstract description 5
- 240000000969 Verbascum thapsus Species 0.000 claims description 18
- 239000000843 powder Substances 0.000 claims description 14
- 229920002678 cellulose Polymers 0.000 claims description 13
- 235000010980 cellulose Nutrition 0.000 claims description 13
- 239000003205 fragrance Substances 0.000 claims description 12
- 239000001913 cellulose Substances 0.000 claims description 11
- 150000004676 glycans Polymers 0.000 claims description 11
- 229920001282 polysaccharide Polymers 0.000 claims description 11
- 239000005017 polysaccharide Substances 0.000 claims description 11
- 150000004804 polysaccharides Polymers 0.000 claims description 11
- 239000005792 Geraniol Substances 0.000 claims description 8
- GLZPCOQZEFWAFX-YFHOEESVSA-N Geraniol Natural products CC(C)=CCC\C(C)=C/CO GLZPCOQZEFWAFX-YFHOEESVSA-N 0.000 claims description 8
- 229930008393 geraniol Natural products 0.000 claims description 8
- 229940113087 geraniol Drugs 0.000 claims description 8
- GLZPCOQZEFWAFX-JXMROGBWSA-N β-Geraniol Chemical compound CC(C)=CCC\C(C)=C\CO GLZPCOQZEFWAFX-JXMROGBWSA-N 0.000 claims description 8
- 210000001736 Capillaries Anatomy 0.000 claims description 7
- 239000000654 additive Substances 0.000 claims description 7
- 238000000034 method Methods 0.000 claims description 7
- 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 6
- 229960004873 LEVOMENTHOL Drugs 0.000 claims description 6
- 229940041616 Menthol Drugs 0.000 claims description 6
- 230000000996 additive Effects 0.000 claims description 5
- 239000000835 fiber Substances 0.000 claims description 5
- 238000000465 moulding Methods 0.000 claims description 5
- 239000004743 Polypropylene Substances 0.000 claims description 3
- 229920002472 Starch Polymers 0.000 claims description 3
- 229920001155 polypropylene Polymers 0.000 claims description 3
- 235000019698 starch Nutrition 0.000 claims description 3
- 238000011049 filling Methods 0.000 claims description 2
- 239000000416 hydrocolloid Substances 0.000 claims description 2
- 239000000077 insect repellent Substances 0.000 claims description 2
- 229920000098 polyolefin Polymers 0.000 claims description 2
- 235000000346 sugar Nutrition 0.000 claims description 2
- 150000008163 sugars Chemical group 0.000 claims description 2
- 230000001225 therapeutic Effects 0.000 claims 1
- 238000010348 incorporation Methods 0.000 abstract description 2
- 239000001993 wax Substances 0.000 description 11
- 150000001299 aldehydes Chemical class 0.000 description 6
- WVDDGKGOMKODPV-UHFFFAOYSA-N benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 6
- HEDRZPFGACZZDS-UHFFFAOYSA-N chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 6
- KJPRLNWUNMBNBZ-QPJJXVBHSA-N cinnamic aldehyde Natural products O=C\C=C\C1=CC=CC=C1 KJPRLNWUNMBNBZ-QPJJXVBHSA-N 0.000 description 6
- 239000000470 constituent Substances 0.000 description 6
- 150000002576 ketones Chemical class 0.000 description 6
- 150000002894 organic compounds Chemical class 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
- 229920000642 polymer Polymers 0.000 description 5
- 238000002360 preparation method Methods 0.000 description 5
- QMVPMAAFGQKVCJ-SNVBAGLBSA-N (R)-(+)-citronellol Natural products OCC[C@H](C)CCC=C(C)C QMVPMAAFGQKVCJ-SNVBAGLBSA-N 0.000 description 4
- CDOSHBSSFJOMGT-JTQLQIEISA-N (R)-linalool Natural products CC(C)=CCC[C@@](C)(O)C=C CDOSHBSSFJOMGT-JTQLQIEISA-N 0.000 description 4
- NEHNMFOYXAPHSD-JTQLQIEISA-N (S)-(-)-citronellal Natural products O=CC[C@@H](C)CCC=C(C)C NEHNMFOYXAPHSD-JTQLQIEISA-N 0.000 description 4
- VAJVDSVGBWFCLW-UHFFFAOYSA-N 3-phenylpropan-1-ol Chemical compound OCCCC1=CC=CC=C1 VAJVDSVGBWFCLW-UHFFFAOYSA-N 0.000 description 4
- KSMVZQYAVGTKIV-UHFFFAOYSA-N Decanal Chemical compound CCCCCCCCCC=O KSMVZQYAVGTKIV-UHFFFAOYSA-N 0.000 description 4
- RRAFCDWBNXTKKO-UHFFFAOYSA-N Eugenol Chemical compound COC1=CC(CC=C)=CC=C1O RRAFCDWBNXTKKO-UHFFFAOYSA-N 0.000 description 4
- UIIMBOGNXHQVGW-UHFFFAOYSA-M NaHCO3 Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 238000002485 combustion reaction Methods 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 238000005755 formation reaction Methods 0.000 description 4
- WTEVQBCEXWBHNA-JXMROGBWSA-N geranial Chemical compound CC(C)=CCC\C(C)=C\C=O WTEVQBCEXWBHNA-JXMROGBWSA-N 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 239000012188 paraffin wax Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- KIUPCUCGVCGPPA-UHFFFAOYSA-N (5-methyl-2-propan-2-ylcyclohexyl) carbonochloridate Chemical compound CC(C)C1CCC(C)CC1OC(Cl)=O KIUPCUCGVCGPPA-UHFFFAOYSA-N 0.000 description 3
- OOCCDEMITAIZTP-QPJJXVBHSA-N Cinnamyl alcohol Chemical compound OC\C=C\C1=CC=CC=C1 OOCCDEMITAIZTP-QPJJXVBHSA-N 0.000 description 3
- CBOQJANXLMLOSS-UHFFFAOYSA-N Ethylvanillin Chemical compound CCOC1=CC(C=O)=CC=C1O CBOQJANXLMLOSS-UHFFFAOYSA-N 0.000 description 3
- 229940117916 cinnamic aldehyde Drugs 0.000 description 3
- 229940073505 ethyl vanillin Drugs 0.000 description 3
- 238000001125 extrusion Methods 0.000 description 3
- YGYAWVDWMABLBF-UHFFFAOYSA-N phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- GRWFGVWFFZKLTI-IUCAKERBSA-N (-)-α-pinene Chemical compound CC1=CC[C@@H]2C(C)(C)[C@H]1C2 GRWFGVWFFZKLTI-IUCAKERBSA-N 0.000 description 2
- 239000001490 (3R)-3,7-dimethylocta-1,6-dien-3-ol Substances 0.000 description 2
- MBAOABFNWSOOLU-UHFFFAOYSA-N 3,3-dimethoxyprop-1-enylbenzene Chemical compound COC(OC)C=CC1=CC=CC=C1 MBAOABFNWSOOLU-UHFFFAOYSA-N 0.000 description 2
- HUMNYLRZRPPJDN-UHFFFAOYSA-N Benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 description 2
- RWCCWEUUXYIKHB-UHFFFAOYSA-N Benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 2
- 229920002301 Cellulose acetate Polymers 0.000 description 2
- 229920000742 Cotton Polymers 0.000 description 2
- ZYGHJZDHTFUPRJ-UHFFFAOYSA-N Coumarin Chemical compound C1=CC=C2OC(=O)C=CC2=C1 ZYGHJZDHTFUPRJ-UHFFFAOYSA-N 0.000 description 2
- 240000003624 Cymbopogon nardus Species 0.000 description 2
- 235000018791 Cymbopogon nardus Nutrition 0.000 description 2
- 239000005770 Eugenol Substances 0.000 description 2
- 229960002217 Eugenol Drugs 0.000 description 2
- 241000134874 Geraniales Species 0.000 description 2
- JARKCYVAAOWBJS-UHFFFAOYSA-N Hexanal Chemical compound CCCCCC=O JARKCYVAAOWBJS-UHFFFAOYSA-N 0.000 description 2
- BJIOGJUNALELMI-ONEGZZNKSA-N Isoeugenol Natural products COC1=CC(\C=C\C)=CC=C1O BJIOGJUNALELMI-ONEGZZNKSA-N 0.000 description 2
- 240000006240 Linum usitatissimum Species 0.000 description 2
- 235000004431 Linum usitatissimum Nutrition 0.000 description 2
- XPCTZQVDEJYUGT-UHFFFAOYSA-N Maltol Chemical compound CC=1OC=CC(=O)C=1O XPCTZQVDEJYUGT-UHFFFAOYSA-N 0.000 description 2
- OSWPMRLSEDHDFF-UHFFFAOYSA-N Methyl salicylate Chemical compound COC(=O)C1=CC=CC=C1O OSWPMRLSEDHDFF-UHFFFAOYSA-N 0.000 description 2
- 238000006845 Michael addition reaction Methods 0.000 description 2
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 2
- DTUQWGWMVIHBKE-UHFFFAOYSA-N Phenylacetaldehyde Chemical compound O=CCC1=CC=CC=C1 DTUQWGWMVIHBKE-UHFFFAOYSA-N 0.000 description 2
- SATCULPHIDQDRE-UHFFFAOYSA-N Piperonal Chemical compound O=CC1=CC=C2OCOC2=C1 SATCULPHIDQDRE-UHFFFAOYSA-N 0.000 description 2
- 239000004793 Polystyrene Substances 0.000 description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N Stearic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
- MWOOGOJBHIARFG-UHFFFAOYSA-N Vanillin Chemical compound COC1=CC(C=O)=CC=C1O MWOOGOJBHIARFG-UHFFFAOYSA-N 0.000 description 2
- HRHOWZHRCRZVCU-AATRIKPKSA-N [(E)-hex-2-enyl] acetate Chemical compound CCC\C=C\COC(C)=O HRHOWZHRCRZVCU-AATRIKPKSA-N 0.000 description 2
- 150000001241 acetals Chemical class 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 235000013871 bee wax Nutrition 0.000 description 2
- 239000012166 beeswax Substances 0.000 description 2
- 235000019445 benzyl alcohol Nutrition 0.000 description 2
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- 235000000484 citronellol Nutrition 0.000 description 2
- RGSFGYAAUTVSQA-UHFFFAOYSA-N cyclopentane Chemical compound C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 239000000446 fuel Substances 0.000 description 2
- VLKZOEOYAKHREP-UHFFFAOYSA-N hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 2
- 229930007744 linalool Natural products 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- KWOLFJPFCHCOCG-UHFFFAOYSA-N methylphenylketone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 2
- PMZURENOXWZQFD-UHFFFAOYSA-L na2so4 Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
- YHQGMYUVUMAZJR-UHFFFAOYSA-N p-Mentha-1,3-diene Chemical compound CC(C)C1=CC=C(C)CC1 YHQGMYUVUMAZJR-UHFFFAOYSA-N 0.000 description 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
- 229920002223 polystyrene Polymers 0.000 description 2
- 229920002689 polyvinyl acetate Polymers 0.000 description 2
- 239000011118 polyvinyl acetate Substances 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- 239000012429 reaction media Substances 0.000 description 2
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 2
- 235000017557 sodium bicarbonate Nutrition 0.000 description 2
- 229910052938 sodium sulfate Inorganic materials 0.000 description 2
- 235000011152 sodium sulphate Nutrition 0.000 description 2
- ULDHMXUKGWMISQ-VIFPVBQESA-N (+)-(4S)-carvone Chemical compound CC(=C)[C@H]1CC=C(C)C(=O)C1 ULDHMXUKGWMISQ-VIFPVBQESA-N 0.000 description 1
- NFLGAXVYCFJBMK-RKDXNWHRSA-N (+)-Isomenthone Natural products CC(C)[C@H]1CC[C@@H](C)CC1=O NFLGAXVYCFJBMK-RKDXNWHRSA-N 0.000 description 1
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- HMKKIXGYKWDQSV-SDNWHVSQSA-N 2-Pentyl-3-phenyl-2-propenal Chemical compound CCCCC\C(C=O)=C/C1=CC=CC=C1 HMKKIXGYKWDQSV-SDNWHVSQSA-N 0.000 description 1
- XSAYZAUNJMRRIR-UHFFFAOYSA-N 2-acetylnaphthalene Chemical compound C1=CC=CC2=CC(C(=O)C)=CC=C21 XSAYZAUNJMRRIR-UHFFFAOYSA-N 0.000 description 1
- PJXHBTZLHITWFX-UHFFFAOYSA-N 2-heptylcyclopentan-1-one Chemical compound CCCCCCCC1CCCC1=O PJXHBTZLHITWFX-UHFFFAOYSA-N 0.000 description 1
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- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
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- ROWKJAVDOGWPAT-UHFFFAOYSA-N acetoin Chemical compound CC(O)C(C)=O ROWKJAVDOGWPAT-UHFFFAOYSA-N 0.000 description 1
- CSCPPACGZOOCGX-UHFFFAOYSA-N acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating Effects 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- 238000007792 addition Methods 0.000 description 1
- 229930006725 alpha-pinene Natural products 0.000 description 1
- 229940095076 benzaldehyde Drugs 0.000 description 1
- NGHOLYJTSCBCGC-VAWYXSNFSA-N benzyl (E)-3-phenylprop-2-enoate Chemical compound C=1C=CC=CC=1/C=C/C(=O)OCC1=CC=CC=C1 NGHOLYJTSCBCGC-VAWYXSNFSA-N 0.000 description 1
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- 235000009120 camo Nutrition 0.000 description 1
- 229930006739 camphene Natural products 0.000 description 1
- 229930007890 camphor Natural products 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000004203 carnauba wax Substances 0.000 description 1
- 235000013869 carnauba wax Nutrition 0.000 description 1
- 229930007075 carvone Natural products 0.000 description 1
- 235000005607 chanvre indien Nutrition 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 229940114081 cinnamate Drugs 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 238000000748 compression moulding Methods 0.000 description 1
- 235000009508 confectionery Nutrition 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000000875 corresponding Effects 0.000 description 1
- 229960000956 coumarin Drugs 0.000 description 1
- 235000001671 coumarin Nutrition 0.000 description 1
- QSJXEFYPDANLFS-UHFFFAOYSA-N diacetyl Chemical group CC(=O)C(C)=O QSJXEFYPDANLFS-UHFFFAOYSA-N 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 229930002886 farnesol Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 150000002194 fatty esters Chemical class 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 229930007855 geranyl acetone Natural products 0.000 description 1
- HNZUNIKWNYHEJJ-FMIVXFBMSA-N geranyl acetone Chemical compound CC(C)=CCC\C(C)=C\CCC(C)=O HNZUNIKWNYHEJJ-FMIVXFBMSA-N 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N glycolaldehyde Chemical compound OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 239000000665 guar gum Substances 0.000 description 1
- 229960002154 guar gum Drugs 0.000 description 1
- 235000010417 guar gum Nutrition 0.000 description 1
- 150000002373 hemiacetals Chemical class 0.000 description 1
- 239000011487 hemp Substances 0.000 description 1
- 235000012765 hemp Nutrition 0.000 description 1
- 239000008079 hexane Substances 0.000 description 1
- 229920001903 high density polyethylene Polymers 0.000 description 1
- 239000004700 high-density polyethylene Substances 0.000 description 1
- 125000001183 hydrocarbyl group Chemical group 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000003456 ion exchange resin Substances 0.000 description 1
- 229920003303 ion-exchange polymer Polymers 0.000 description 1
- 229930002839 ionones Natural products 0.000 description 1
- 235000001510 limonene Nutrition 0.000 description 1
- 229930007650 limonene Natural products 0.000 description 1
- 229940087305 limonene Drugs 0.000 description 1
- 229920001684 low density polyethylene Polymers 0.000 description 1
- 239000004702 low-density polyethylene Substances 0.000 description 1
- 229940049920 malate Drugs 0.000 description 1
- BJEPYKJPYRNKOW-UHFFFAOYSA-L malate(2-) Chemical compound [O-]C(=O)C(O)CC([O-])=O BJEPYKJPYRNKOW-UHFFFAOYSA-L 0.000 description 1
- 229940043353 maltol Drugs 0.000 description 1
- 235000012766 marijuana Nutrition 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 229930007503 menthone Natural products 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 229960001047 methyl salicylate Drugs 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- UAVOCTDYPKOULU-UHFFFAOYSA-N methylchloranuidyl formate Chemical compound C[Cl-]OC=O UAVOCTDYPKOULU-UHFFFAOYSA-N 0.000 description 1
- 239000004200 microcrystalline wax Substances 0.000 description 1
- 235000019808 microcrystalline wax Nutrition 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000006011 modification reaction Methods 0.000 description 1
- 229940067137 musk ketone Drugs 0.000 description 1
- 239000000025 natural resin Substances 0.000 description 1
- 230000001264 neutralization Effects 0.000 description 1
- 230000001473 noxious Effects 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- MYMOFIZGZYHOMD-UHFFFAOYSA-N oxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 230000002085 persistent Effects 0.000 description 1
- 229940100595 phenylacetaldehyde Drugs 0.000 description 1
- 125000000286 phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 1
- 229940081310 piperonal Drugs 0.000 description 1
- 229920001490 poly(butyl methacrylate) polymer Polymers 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920005594 polymer fiber Polymers 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 230000002028 premature Effects 0.000 description 1
- 238000000197 pyrolysis Methods 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 230000035943 smell Effects 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 230000002459 sustained Effects 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 229930007823 thymol Natural products 0.000 description 1
- 229960000790 thymol Drugs 0.000 description 1
- WBYWAXJHAXSJNI-VOTSOKGWSA-M trans-cinnamate Chemical compound [O-]C(=O)\C=C\C1=CC=CC=C1 WBYWAXJHAXSJNI-VOTSOKGWSA-M 0.000 description 1
- 238000005292 vacuum distillation Methods 0.000 description 1
- 229940117960 vanillin Drugs 0.000 description 1
- 235000012141 vanillin Nutrition 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 230000016776 visual perception Effects 0.000 description 1
Abstract
This invention provides a wick composition which is comprised of a polymeric strand such as polyethylene, which has a content of particulate polysaccharidic filler ingredient and air freshener ingredient. The wick is adapted for incorporation in a candle body. When the wick is ignited, it combusts with a controlled release of the air freshener ingredient into the atmosphere.
Description
POLYMERIC COMPOSITION OF PABILO FOR REFRIGERATING AIR CANDLE PRODUCTS
BACKGROUND OF THE INVENTION This invention relates generally to the dispersion of an air freshener of a candle product. More specifically, this invention relates to a wick composition having an air freshening constituent content which is released under wick combustion conditions. The candles have been known and used since the first civilizations. A conventional candle is formed of a solid or semi-solid body of wax such as paraffin wax, beeswax, and contains a fibrous wick of axially embedded fuel. When the wick of a candle is lit, the heat generated melts the solid wax, and the resulting liquid flows to the wick by capillary action and burns. More recently, waxes have been developed that are pleasant to smell as well as to the sense of sight. This type of candles, usually incorporates a fragrance oil in the body of the wax. As the wax melts into a lit candle, there is a release of the fragrance oil from the accumulation of the liquid wax. Conventional fragrance candles have disadvantages due to cost and other considerations. The incorporation of fragrance oil in candle wax is difficult to achieve in an amount that ensures the release of an adequate level of fragrance in the atmosphere during burning of the candle. In addition, the incorporated fragrance tends to migrate and prematurely volatilize from the body of the wax. The fragrance also softens the body of the candle, and there is an undesirable loss of rigidity in the structure of the candle. There is a continuing interest to develop an improved fragrance and other types of air freshener candles. Accordingly, it is an object of this invention to provide an air freshening candle product which releases air freshener in the atmosphere only under burning conditions of the lit candle. It is a further object of the invention to provide a wick composition which has an air freshening constituent content, and which is adapted to be incorporated into a candle body. It is a further object of this invention to provide a wicking composition which can be produced by a continuous molding process. Other objects and advantages of the present invention will be apparent from the description and the appended examples. Publications of interest of background in connection with the present invention include U.S. Patent Nos. 1,974,037; 2,090,297; 2,818,615; 2,829,511; 3,560,122; 3,630,697; and 3,940,233; incorporated by reference.
The E.U.A. No. 2,829,511, describes a wick structure composed of a central cord of cellulose acetate in combination with an external mesh of cotton fibers. The E.U.A. No. 3,560,122 discloses a wick composition which is composed of paraffin wax, polyethylene, and particulate palladium clay. DESCRIPTION OF THE INVENTION One or more objectives of the present invention are achieved by providing a wick composition comprising a polymeric yarn which contains (a) between about 2-40 weight percent of the polysaccharide filling ingredient in particles, and (b) between about 0.05-20 weight percent of air freshening ingredient. The wick composition is usually an elongated yarn having a diameter between about 0.2-0.8 centimeters. In another embodiment, this invention provides a candle product having an axial wick component which comprises a polymeric yarn containing (a) between about 2-40 weight percent particulate polysaccharide filler ingredient, and (b) ) between about 0.05-20 percent by weight of air freshening ingredient. The polymeric matrix of a wick composition of the invention is preferably selected from the class of thermoplastic resins which are generally adapted for the formation of fibers by processes such as extrusion or compression molding. It is preferred that the polymer be composed of elements which do not turn into noxious vapors, such as carbon, hydrogen and oxygen, under combustion conditions.
Equipment and processes for forming polymer fibers by extrusion are described in publications such as U.S. Patent Nos. 3,065,502; 3,351,695; 3,577,588; 4,134,714; 4,302,409; and 5,320,798; incorporated by reference. A polymeric wick yarn can be composed of multiple filaments. Suitable fiber forming polymers include polyolefin hydrocarbyl derivatives such as high and low density polyethylene, high and low density polypropylene, polybutene, polystyrene, and the like. Other suitable types of polymers include polyvinyl acetate, and acrylate resins such as polymethyl acrylate, polymethyl methacrylate, polybutyl methacrylate, poly (ethylacrylate / ethylene), and the like. Other types of polymers such as thermosetting resins can be used, by pressure molding a resin powder mixture, polysaccharide filler and cooling ingredients.
Other components may be included in a wicking composition such as stearic acid, polyoxyalkylene glycol, and the like. The polysaccharide filler ingredient of a wick composition of the invention, usually has the form of powder, or the form of fine fibers which have an average height between about 0.3-3 centimeters. The term "polysaccharide", as used herein, means that it includes neutral products such as sugars, starches, hydrocolloid gums, celluloses, and the like. A cellulose filler ingredient can be obtained from vegetable sources such as cotton, flax, flax fiber, hemp, jute, wood pulp, and the like. A cellulose filler may be in the form of substituted derivatives such as cellulose acetate or methyl cellulose. The term "celluloseX" as used herein, refers to a β-glucosidic polysaccharide corresponding to the formula: wherein n is an integer which provides an average molecular weight between about 100,000-2,000,000. of the present invention can be produced using conventional candle making methods such as molding, submerging, and the like The fuel body of a candle product is usually a thermoplastic blend of organic materials such as beeswax, paraffin wax , mountain wax, carnauba wax, microcrystalline wax, fatty alcohols, fatty acids, fatty esters, natural and synthetic resins and the like, a wick usually extends longitudinally through a candle body, more than a single wick can be used in one separate relationship, but usually a single wicking component is centrally arranged in a configured candlestick body. n candle wick, the wick is adapted to burn gradually, so that the wick and body of the candle is consumed. When in a candle body, a wick structure of the present invention, after being turned on, has sufficient porosity to absorb the wax of the candle cast in the wick by means of capillary action for combustion during the use of the candle. The transport of the molten wax can be improved by one or more capillary openings extending axially along the surface of the wick filament. The term "air freshener", as used herein, means that it includes fragrances such as geraniol, insect repellents such as citronella, and therapeutic agents such as menthol. An air freshener of a wick composition of the present invention can be any inherently volatile organic compound which is capable of dispersing in the atmosphere when the wicking composition is burned. Suitable volatile air freshening compounds include limonene, α-terpinene, α-pinene, camphene, undecanol, 4-isopropylcyclohexanol, geraniol, linalool, citronellol, farnesol, menthol, 3-trans-isoalkanecyclohexane., benzyl alcohol, 2-phenylethyl alcohol, 3-phenylpropanol, 3-methyl-5-phenylpentanol, cinnamic alcohol, isoborneol, thymol, eugenol, isoeugenol, anise alcohol, methyl salicylate, and the like. Other suitable air-flavoring compounds include aldehydes and ketones such as hexanal, decanal, 2-methyldecanal, trans-2-hexanal, acetoin, diacetyl, geranial, citronellal, methoxydihydro-citronellal, menthone, carvone, camphor, fenone, ionone, irona, damascone, cedrile methyl ketone, muscone, civetone, carboxyaldehyde of 2,4-dimethyl-3-cyclohexane, 2-heptylcyclopentanone, cis-jasmona, dihydrojasmone, cyclopentadecanone, benzaldehyde, phenylacetaldehyde, dehydrocinlaldehyde, cinnamaldehyde, α-amylcinnamaldehyde, acetophenone, benzylacetone , benzophenone, piperonal, and the like. Other suitable air freshening compounds include esters such as trans-2-hexenyl acetate, allyl 3-cyclopropionate, methyl cinnamate, benzyl cinnamate, phenylethyl cinnamate, and the like. Other suitable air freshening compounds include crystalline fragrance materials with a high vapor pressure, such as vanillin, ethyl vanillin, coumarin, tonal, caloe, heliotropene, musk xylol, musk ketone, benzophenone, raspberry ketone, beta methyl naphthyl ketone, phenylethyl salicylate, veltol, maltol, maple lactone, proeugenol acetate, evernil, and the like. The present invention also contemplates a wick composition in which the air freshener is a constituent of a non-volatile air freshening release additive. The constituent of air freshener is released by pyrolysis under wicking conditions. The term "non-volatile", as used herein, refers to an organic compound which has a low pressure vapor under ambient conditions. Chemical bonding of a volatile alcohol air freshener such as geraniol or menthol, to another organic compound to form a non-volatile organic derivative, can be completed by the formation of a carbonate ester ligation (as illustrated in Example V) : OO
II II R-OCCL + HO-R1? R-OCO-R1
The chemical linkage of an aldehyde, such as citronellal, or a ketone, such as fencone, to another organic compound, may be completed by the formation of a hemiacetal (ketal) and / or acetal (ketal) ligation under acidic conditions: HO- CH2 OH HO-CH2 III R-CHO + HO-CH-R1? R-CH- O- CH-R1 H +
HO-CH2 R2 O -CH2 I \ / I R2-CO-R3 + HO-CH-R1? CIH "/ \ I R3 O - CH-R1 Chemical bonding of an ester such as air freshener of cinnamate Phenylethyl malate to another organic compound, can be completed by a Michael addition reaction under alkaline conditions: R1O2C-CH = CH- R + HO-R2> OH-
R1O2C-CH3-CH-O-R:
The Michael addition reaction is described in publications such as E.U.A. 2,415,040 and E.U.A. 5,569,779, incorporated by reference. Another chemical means for the formation of a ligation between an air freshener of volatile alcohol and another organic compound is by the use of an alcohol derivative of epichlorohydrin under alkaline reaction conditions: O / \ RO-CH2-CH-CH2 + HO -R1? OH "OH R-O-CH3-CH-CH2-O-R1
A wick composition of the present invention provides significant advantages not previously contemplated in the candle making art.
A wick composition of the invention can be efficiently manufactured in large volume by means of a continuous molding process such as filament forming extrusion. The air freshener ingredient is released only when the composition of the wick is burning. The air flavoring is released at a steady sustained rate. Since there is no need for an air freshener such as a fragrance oil dispersed within a candle product of the present invention, there is no premature loss of air freshener by migration and evaporation of the candle body, and there is no softening or loss of rigidity in the body of the sail. The following examples further illustrate the present invention. The specific components and ingredients are presented as usual and various modifications may be derived in view of the above description within the scope of the invention. EXAMPLE I This example illustrates the preparation of a wick composition according to the present invention. The cellulose powder was impregnated with geraniol, and the combination is mixed with polyethylene powder (MP 120EC). The mixture contains 18 weight percent cellulose powder and 1.5 weight percent geraniol. The mixture was passed through an extruder under heat and pressure to form a continuous wick composition yarn having a diameter of 5 millimeters, and having multiple capillary openings axially along the yarn surface. A cut thread section was completely consumed when it is turned on. The combustion of the wick releases a floral aroma that is characteristic of geraniol. A formed paraffin candle (MP 63EC) is drilled in the center, and a section of the wick was inserted. When the wick was lit, the flame persisted until the candle was consumed. A floral rose scent was released during the burning of the candle. Similar results were obtained when the starch or guar gum was substituted for the cellulose powder. EXAMPLE II This Example illustrates the preparation of a wick composition according to the present invention. The polypropylene powder (MP 110EC) was mixed with a combination of cellulose powder and ethyl vanillin. The mixture contains 22 weight percent cellulose powder and 3 weight percent ethyl vanillin. The mixture was passed through an extruder under heat and pressure to form a continuous wick composition yarn having a diameter of 3 milliliters, and having multiple axial capillary openings along the surface of the yarn. A section of cut string was completely consumed when it was turned on. In the atmosphere a sweet aroma similar to that of vanilla was detected during the burning of the wick. A release of similar air freshener is observed when the wick burns inside a candle body. EXAMPLE III This example illustrates the preparation of polysaccharide derivatives releasing non-volatile air freshener from ketone and aldehyde air flavoring constituents.
Glucose (180 g) was dissolved in dimethylformamide (4 liters), and Amberlite 1R-120 (100 g) was added. The mixture was heated to 80 ° C, and cinnamaldehyde dimethyl acetal (178 g) was added in portions over a period of three hours. After the addition, the mixture was heated for an additional hour. The ion exchange resin was removed by filtration, and the solvent and excess of cinnamaldehyde dimethyl acetal were removed by vacuum distillation. The residual material was recrystallized with 95% ethanol to give 150 g of the 4-6-0-cinnamylidene-D-glucopyranose product. Following the same procedure, the acetal and ketal derivatives of D-glucopyranose were synthesized from the following aldehydes and ketones:
Decanal Mentona Geranial Fencone Citronella acetophenone benzaldehyde benzophenone phenylacetaldehyde Camphor dihydro cinnamaldehyde geranylacetone
The polyethylene powder (MO 120EC) was mixed with 10 weight percent cellulose powder, and 2 weight percent air freshening release additive of 4-6-0-cinnamylidene-D-glucopyranose. the mixture was passed through an extruder under heat and pressure to form a continuous wick composition yarn having a diameter of 3.5 millimeters. A section of the thread was lit, and the flame persists until the wick section is completely consumed. A slight essence of cinnamaldehyde could be felt in the atmosphere. When a wick composition contains 4 percent of the air freshener release additive, the aroma of cinnamaldehyde is strong and persistent. Similar olfactory results were obtained with each of the aldehyde and ketone air freshener release derivatives synthesized as additives in the wick compositions of the present invention. EXAMPLE IV This Example illustrates the preparation of methyl chloroformate.
A reactor in an ice / dry bath (-75EC) was charged with liquid phosgene (117 g). Menthol (130 g) dissolved in 500 mL of cyclopentane was added by dripping to the phosgene with stirring. The reaction medium was heated to reflux for six hours at room temperature. Excess phosgene and cyclopentane were removed under reduced pressure. The recovered menthyl chloroformate was dissolved in diethyl ether (300 mL), and the solution was washed with aqueous sodium bicarbonate, and then with distilled water. The liquid medium was dried over sodium sulfate, and the solvent was removed under reduced pressure to produce a purified menthyl chloroformate. EXAMPLE V The Example illustrates the preparation of a non-volatile air freshening release bicarbonate ester with alcohol air freshening constituents.
To a cooled solution of pyridine (25 mL) in chloroform (500 mL) was added with glycoaldehyde stirring (10 g, 0.167 mol) A solution of menthyl chloroformate (36.5 g;
0. 167 moles) in chloroform (100 mL). Stirring was continued for 30 minutes at OEC, then for 18 hours at room temperature: The reaction medium was washed with aqueous sodium bicarbonate, and then dried over sodium sulfate. The solvent was removed under reduced pressure. The residual product was recrystallized from chloroform: hexane to yield 16 g of 2.5-bis (menthyl-carbonyloxy) -1,4-dioxane. Following the same procedure, the dicarbonate ester derivatives of the following alcohols were synthesized: geraniol Eugenol linalool 3-phenylpropanol citronellol cinnamyl alcohol benzyl alcohol terpineol
The polystyrene powder (MP 115EC) was mixed with 30 weight percent cellulose powder, and 6 weight percent air freshener release additive from 2,5-bis (menthylcarbonyloxy) -1,4-dioxane . The mixture was passed through an extruder under heat and pressure to form a continuous wick composition yarn having a diameter of 4 millimeters, and having multiple capillary openings along the yarn surface.
A section of thread cut is lit, and the flame persists until the wick section is completely consumed. A distinct menthol aroma is detected in the atmosphere. Similar olfactory results are obtained with each of the other aldehyde and ketone air freshener release derivatives synthesized as additives in wick compositions of the present invention.
The release of similar air freshener was obtained when a wick burns inside a candle body. Similar results were obtained when the polymer ingredient is polyvinyl acetate.
Claims (18)
- CLAIMS 1. A candle wick comprising a polymeric thread which contains (a) between 2 and 40 weight percent particulate polysaccharide filler ingredient, and (b) between 0.05 and 30 weight percent refreshing ingredient of air which is released only when the wick burns.
- 2. The candle wick according to claim 1, which is produced by means of a continuous molding process.
- The candle wick according to claim 1, wherein the polymeric thread is a filament which has at least one capillary opening extending axially along the surface of the filament.
- 4. The candle wick according to claim 1, wherein the polymeric thread comprises polyolefin filament.
- The candle wick according to claim 1, wherein the polymeric yarn is selected from the group consisting of polyethylene and polypropylene filaments.
- 6. The candle wick according to claim 1, wherein the polymeric thread comprises multiple filaments.
- The candle wick according to claim 1, wherein the particulate polysaccharide filling comprises powder or fine fibers.
- 8. The candle wick according to claim 1, wherein the polysaccharide filler is selected from the group consisting of sugars, starches, hydrocolloid gums and celluloses.
- 9. The candle wick according to claim 1, wherein the polysaccharide filler comprises cellulose or a cellulose derivative.
- The candle wick according to claim 1, wherein the air freshener comprises a fragrance ingredient.
- 11. The candle wick according to claim 1, wherein the air freshener comprises an insect repellent ingredient.
- 12. The candle wick according to claim 1, wherein the air freshener comprises a therapeutic ingredient.
- 13. The candle wick according to claim 1, wherein the air freshening ingredient comprises geraniol.
- 14. The candle wick according to claim 1, wherein the air freshening ingredient comprises citranelal.
- 15. The candle wick according to claim 1, wherein the air freshening ingredient comprises menthol.
- 16. The candle wick according to claim 1, wherein the air freshening ingredient has the form of a non-volatile air freshening release additive, and wherein the air freshener is released into the atmosphere when it burns. the wick
- 17. The candle wick according to claim 1, which is an elongated polymeric thread having a diameter between 0.2 and 0.8. and which is adapted to be incorporated in a sail product.
- 18. A candle product having an axial wick according to any of claims 1 to 17.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US08915160 | 1997-08-20 |
Publications (1)
Publication Number | Publication Date |
---|---|
MXPA00001755A true MXPA00001755A (en) | 2001-05-17 |
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