JPH048366A - Granular aromatic deodorant - Google Patents
Granular aromatic deodorantInfo
- Publication number
- JPH048366A JPH048366A JP2108763A JP10876390A JPH048366A JP H048366 A JPH048366 A JP H048366A JP 2108763 A JP2108763 A JP 2108763A JP 10876390 A JP10876390 A JP 10876390A JP H048366 A JPH048366 A JP H048366A
- Authority
- JP
- Japan
- Prior art keywords
- acid
- zinc
- parts
- perfume
- deodorizing
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 125000003118 aryl group Chemical group 0.000 title claims abstract description 28
- 239000002781 deodorant agent Substances 0.000 title abstract 2
- 230000001877 deodorizing effect Effects 0.000 claims abstract description 31
- 239000002253 acid Substances 0.000 claims abstract description 16
- 150000003752 zinc compounds Chemical class 0.000 claims abstract description 9
- 150000007524 organic acids Chemical class 0.000 claims abstract description 8
- 125000001931 aliphatic group Chemical group 0.000 claims abstract description 5
- 239000003205 fragrance Substances 0.000 claims description 18
- 239000008187 granular material Substances 0.000 claims description 6
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 abstract description 13
- 239000011787 zinc oxide Substances 0.000 abstract description 7
- FMRLDPWIRHBCCC-UHFFFAOYSA-L Zinc carbonate Chemical compound [Zn+2].[O-]C([O-])=O FMRLDPWIRHBCCC-UHFFFAOYSA-L 0.000 abstract description 6
- 229920000642 polymer Polymers 0.000 abstract description 6
- 239000011667 zinc carbonate Substances 0.000 abstract description 6
- 235000004416 zinc carbonate Nutrition 0.000 abstract description 6
- 229910000010 zinc carbonate Inorganic materials 0.000 abstract description 6
- 230000000873 masking effect Effects 0.000 abstract description 5
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 abstract description 4
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 abstract description 4
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 abstract description 3
- 229910052725 zinc Inorganic materials 0.000 abstract description 3
- 239000011701 zinc Substances 0.000 abstract description 3
- 244000178870 Lavandula angustifolia Species 0.000 abstract description 2
- 235000010663 Lavandula angustifolia Nutrition 0.000 abstract description 2
- 239000001102 lavandula vera Substances 0.000 abstract description 2
- 235000018219 lavender Nutrition 0.000 abstract description 2
- WGIWBXUNRXCYRA-UHFFFAOYSA-H trizinc;2-hydroxypropane-1,2,3-tricarboxylate Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O.[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O WGIWBXUNRXCYRA-UHFFFAOYSA-H 0.000 abstract description 2
- 239000011592 zinc chloride Substances 0.000 abstract description 2
- 235000005074 zinc chloride Nutrition 0.000 abstract description 2
- 239000011746 zinc citrate Substances 0.000 abstract description 2
- 235000006076 zinc citrate Nutrition 0.000 abstract description 2
- 229940068475 zinc citrate Drugs 0.000 abstract description 2
- SRWMQSFFRFWREA-UHFFFAOYSA-M zinc formate Chemical compound [Zn+2].[O-]C=O SRWMQSFFRFWREA-UHFFFAOYSA-M 0.000 abstract description 2
- NWONKYPBYAMBJT-UHFFFAOYSA-L zinc sulfate Chemical compound [Zn+2].[O-]S([O-])(=O)=O NWONKYPBYAMBJT-UHFFFAOYSA-L 0.000 abstract description 2
- 229960001763 zinc sulfate Drugs 0.000 abstract description 2
- 229910000368 zinc sulfate Inorganic materials 0.000 abstract description 2
- HJSYJHHRQVHHMQ-TYYBGVCCSA-L zinc;(e)-but-2-enedioate Chemical compound [Zn+2].[O-]C(=O)\C=C\C([O-])=O HJSYJHHRQVHHMQ-TYYBGVCCSA-L 0.000 abstract description 2
- ZPEJZWGMHAKWNL-UHFFFAOYSA-L zinc;oxalate Chemical compound [Zn+2].[O-]C(=O)C([O-])=O ZPEJZWGMHAKWNL-UHFFFAOYSA-L 0.000 abstract description 2
- 239000002304 perfume Substances 0.000 abstract 6
- 238000006243 chemical reaction Methods 0.000 abstract 1
- 238000000465 moulding Methods 0.000 abstract 1
- 239000000203 mixture Substances 0.000 description 16
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 15
- 239000001993 wax Substances 0.000 description 12
- 239000003795 chemical substances by application Substances 0.000 description 9
- 235000019645 odor Nutrition 0.000 description 9
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 8
- -1 diphenyl ether tetracarboxylic acid Chemical class 0.000 description 8
- 239000000178 monomer Substances 0.000 description 7
- 238000001514 detection method Methods 0.000 description 6
- 239000011230 binding agent Substances 0.000 description 5
- 229920001400 block copolymer Polymers 0.000 description 5
- 229920000578 graft copolymer Polymers 0.000 description 5
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 5
- ARCGXLSVLAOJQL-UHFFFAOYSA-N trimellitic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C(C(O)=O)=C1 ARCGXLSVLAOJQL-UHFFFAOYSA-N 0.000 description 5
- 235000014692 zinc oxide Nutrition 0.000 description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
- 150000007513 acids Chemical class 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000001530 fumaric acid Substances 0.000 description 4
- 229920001519 homopolymer Polymers 0.000 description 4
- YDSWCNNOKPMOTP-UHFFFAOYSA-N mellitic acid Chemical compound OC(=O)C1=C(C(O)=O)C(C(O)=O)=C(C(O)=O)C(C(O)=O)=C1C(O)=O YDSWCNNOKPMOTP-UHFFFAOYSA-N 0.000 description 4
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 4
- 229920005604 random copolymer Polymers 0.000 description 4
- 241000207199 Citrus Species 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- UJMDYLWCYJJYMO-UHFFFAOYSA-N benzene-1,2,3-tricarboxylic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1C(O)=O UJMDYLWCYJJYMO-UHFFFAOYSA-N 0.000 description 3
- 125000002843 carboxylic acid group Chemical group 0.000 description 3
- 239000001913 cellulose Substances 0.000 description 3
- 229920002678 cellulose Polymers 0.000 description 3
- 235000020971 citrus fruits Nutrition 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 239000005038 ethylene vinyl acetate Substances 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 150000002894 organic compounds Chemical class 0.000 description 3
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 3
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 125000000542 sulfonic acid group Chemical group 0.000 description 3
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 3
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 2
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 2
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 2
- 239000001856 Ethyl cellulose Substances 0.000 description 2
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 description 2
- 229920002125 Sokalan® Polymers 0.000 description 2
- 235000021355 Stearic acid Nutrition 0.000 description 2
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- CVGUHCZVNLAROZ-UHFFFAOYSA-N acetic acid;phthalic acid;sulfuric acid Chemical class CC(O)=O.OS(O)(=O)=O.OC(=O)C1=CC=CC=C1C(O)=O CVGUHCZVNLAROZ-UHFFFAOYSA-N 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 229910021529 ammonia Inorganic materials 0.000 description 2
- 159000000032 aromatic acids Chemical class 0.000 description 2
- 238000003287 bathing Methods 0.000 description 2
- 239000001055 blue pigment Substances 0.000 description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
- 150000001735 carboxylic acids Chemical class 0.000 description 2
- 229920002301 cellulose acetate Polymers 0.000 description 2
- HNEGQIOMVPPMNR-IHWYPQMZSA-N citraconic acid Chemical compound OC(=O)C(/C)=C\C(O)=O HNEGQIOMVPPMNR-IHWYPQMZSA-N 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- 229920001249 ethyl cellulose Polymers 0.000 description 2
- 235000019325 ethyl cellulose Nutrition 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 229910000037 hydrogen sulfide Inorganic materials 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 2
- UTOPWMOLSKOLTQ-UHFFFAOYSA-N octacosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCC(O)=O UTOPWMOLSKOLTQ-UHFFFAOYSA-N 0.000 description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 2
- 239000012188 paraffin wax Substances 0.000 description 2
- WLJVNTCWHIRURA-UHFFFAOYSA-N pimelic acid Chemical compound OC(=O)CCCCCC(O)=O WLJVNTCWHIRURA-UHFFFAOYSA-N 0.000 description 2
- 239000004584 polyacrylic acid Substances 0.000 description 2
- 229920002689 polyvinyl acetate Polymers 0.000 description 2
- 239000011118 polyvinyl acetate Substances 0.000 description 2
- 229920002451 polyvinyl alcohol Polymers 0.000 description 2
- CYIDZMCFTVVTJO-UHFFFAOYSA-N pyromellitic acid Chemical compound OC(=O)C1=CC(C(O)=O)=C(C(O)=O)C=C1C(O)=O CYIDZMCFTVVTJO-UHFFFAOYSA-N 0.000 description 2
- 239000001054 red pigment Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000000344 soap Substances 0.000 description 2
- 239000008117 stearic acid Substances 0.000 description 2
- 235000002906 tartaric acid Nutrition 0.000 description 2
- 239000011975 tartaric acid Substances 0.000 description 2
- 239000001052 yellow pigment Substances 0.000 description 2
- ONDPHDOFVYQSGI-UHFFFAOYSA-N zinc nitrate Chemical compound [Zn+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O ONDPHDOFVYQSGI-UHFFFAOYSA-N 0.000 description 2
- OYHQOLUKZRVURQ-NTGFUMLPSA-N (9Z,12Z)-9,10,12,13-tetratritiooctadeca-9,12-dienoic acid Chemical compound C(CCCCCCC\C(=C(/C\C(=C(/CCCCC)\[3H])\[3H])\[3H])\[3H])(=O)O OYHQOLUKZRVURQ-NTGFUMLPSA-N 0.000 description 1
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 description 1
- RTBFRGCFXZNCOE-UHFFFAOYSA-N 1-methylsulfonylpiperidin-4-one Chemical compound CS(=O)(=O)N1CCC(=O)CC1 RTBFRGCFXZNCOE-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- OBETXYAYXDNJHR-UHFFFAOYSA-N 2-Ethylhexanoic acid Chemical compound CCCCC(CC)C(O)=O OBETXYAYXDNJHR-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- SHHKMWMIKILKQW-UHFFFAOYSA-N 2-formylbenzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1C=O SHHKMWMIKILKQW-UHFFFAOYSA-N 0.000 description 1
- ZMPRRFPMMJQXPP-UHFFFAOYSA-N 2-sulfobenzoic acid Chemical compound OC(=O)C1=CC=CC=C1S(O)(=O)=O ZMPRRFPMMJQXPP-UHFFFAOYSA-N 0.000 description 1
- KVAXJTKYJLYPPP-UHFFFAOYSA-N 2-sulfopentanoic acid Chemical compound CCCC(C(O)=O)S(O)(=O)=O KVAXJTKYJLYPPP-UHFFFAOYSA-N 0.000 description 1
- WBGKAOURNYRYBT-UHFFFAOYSA-N 2-sulfopropanoic acid Chemical compound OC(=O)C(C)S(O)(=O)=O WBGKAOURNYRYBT-UHFFFAOYSA-N 0.000 description 1
- HNNQYHFROJDYHQ-UHFFFAOYSA-N 3-(4-ethylcyclohexyl)propanoic acid 3-(3-ethylcyclopentyl)propanoic acid Chemical compound CCC1CCC(CCC(O)=O)C1.CCC1CCC(CCC(O)=O)CC1 HNNQYHFROJDYHQ-UHFFFAOYSA-N 0.000 description 1
- SDGNNLQZAPXALR-UHFFFAOYSA-N 3-sulfophthalic acid Chemical compound OC(=O)C1=CC=CC(S(O)(=O)=O)=C1C(O)=O SDGNNLQZAPXALR-UHFFFAOYSA-N 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
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- 239000004606 Fillers/Extenders Substances 0.000 description 1
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- 239000000025 natural resin Substances 0.000 description 1
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 125000002270 phosphoric acid ester group Chemical group 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920005596 polymer binder Polymers 0.000 description 1
- 239000002491 polymer binding agent Substances 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- UORVCLMRJXCDCP-UHFFFAOYSA-N propynoic acid Chemical compound OC(=O)C#C UORVCLMRJXCDCP-UHFFFAOYSA-N 0.000 description 1
- 229910052979 sodium sulfide Inorganic materials 0.000 description 1
- GRVFOGOEDUUMBP-UHFFFAOYSA-N sodium sulfide (anhydrous) Chemical compound [Na+].[Na+].[S-2] GRVFOGOEDUUMBP-UHFFFAOYSA-N 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 150000003628 tricarboxylic acids Chemical class 0.000 description 1
- 150000003751 zinc Chemical class 0.000 description 1
- 239000004246 zinc acetate Substances 0.000 description 1
- LRXTYHSAJDENHV-UHFFFAOYSA-H zinc phosphate Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O LRXTYHSAJDENHV-UHFFFAOYSA-H 0.000 description 1
- 229910000165 zinc phosphate Inorganic materials 0.000 description 1
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 1
Abstract
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明は、顆粒状芳香脱臭剤に関し、更に詳しくは、各
種悪臭発生源の悪臭除去に有用な顆粒状芳香脱臭剤に関
する。DETAILED DESCRIPTION OF THE INVENTION (Industrial Application Field) The present invention relates to a granular aromatic deodorizer, and more particularly to a granular aromatic deodorizer useful for removing malodors from various malodor sources.
(従来の技術及びその問題点) 従来、各種の悪臭源に対して使用する脱臭剤とる。(Conventional technology and its problems) Conventionally, deodorizing agents have been used against various sources of bad odors.
一方、悪臭をマスキングして悪臭をあまり感じさせない
ものとして芳香剤が使用されている。On the other hand, air fresheners are used to mask bad odors so that they are less noticeable.
前記脱臭剤の場合には、僅かでも悪臭が残ると、その悪
臭が感じらt、物理的には大部分の悪臭源を除去するも
のの、官能的には悪臭の除去効果が少なく、又、悪臭の
除去効果の持続性がなく、いずれ悪臭の除去効果が失わ
れる。In the case of the above-mentioned deodorizer, if even a small amount of bad odor remains, the bad odor will not be felt, and although it physically removes most of the sources of bad odor, it has little effect on removing bad odor sensually. The odor removal effect is not sustainable, and the odor removal effect will eventually be lost.
又、前記芳香剤の場合には、悪臭は減少しないので、用
途、場所によっては一層不快な臭気を感じさせるという
欠点がある、
従って、本発明の目的は、脱臭効果及びマスキング効果
の両方を有し、脱臭効果がなくなっても、マスキング効
果によって消臭効果を持続させる芳香脱臭剤を提供する
ことである。Furthermore, in the case of the above-mentioned fragrances, the bad odor does not decrease, so there is a drawback that depending on the use and location, the fragrance may make the user feel even more unpleasant. Therefore, the object of the present invention is to use a fragrance that has both a deodorizing effect and a masking effect. However, it is an object of the present invention to provide an aromatic deodorizing agent that maintains the deodorizing effect by a masking effect even if the deodorizing effect is lost.
(問題点を解決する為の手段) 上記目的は以下の本発明によって達成される。(Means for solving problems) The above objects are achieved by the present invention as described below.
即ち、本発明は、香料と亜鉛化合物と有機酸とを顆粒状
に成形してなることを特徴とする特許芳香脱臭剤である
。That is, the present invention is a patented aromatic deodorizer characterized by forming a fragrance, a zinc compound, and an organic acid into granules.
(作 用)
香料と脱臭剤を顆粒状に成形することによって、脱臭剤
の脱臭効果を失うことなく、香料によってマスキング効
果を発揮させることが出来る。(Function) By forming the fragrance and deodorizer into granules, the masking effect can be exerted by the fragrance without losing the deodorizing effect of the deodorizer.
(好ましい実施態様)
次に好ましい実施態様を挙げて本発明を更に詳細に説明
する。(Preferred Embodiments) Next, the present invention will be described in more detail by citing preferred embodiments.
本発明において使用する香料とは、後述する脱臭成分と
化学反応しない香料であり、例えば、シトラス、フロー
ラル、ローズ、ラベンダー、サンダール等の名称で一般
的に使用されている香料が使用出来る。又、これらの香
料として、他物質でマイクロカプセル化したものを使用
すれば、芳香持続時間を長期に維持することが出来て好
ましい。The fragrance used in the present invention is a fragrance that does not chemically react with the deodorizing component described below, and for example, fragrances commonly used under names such as citrus, floral, rose, lavender, sandal, etc. can be used. It is also preferable to use these fragrances that have been microencapsulated with other substances because the fragrance duration can be maintained for a long period of time.
上記香料の使用量は任意であるが、好適には後述の脱臭
成分100重量部当たり0.5〜50重量部程度である
。The amount of the fragrance to be used is arbitrary, but preferably about 0.5 to 50 parts by weight per 100 parts by weight of the deodorizing component described below.
本発明で使用する個々の脱臭成分それ自体はいずれも公
知の化合物であり、亜鉛化合物としては、種々の亜鉛化
合物、例えば、酸化亜鉛、硫酸亜鉛、塩化亜鉛、リン酸
亜鉛、硝酸亜鉛、炭酸亜鉛等の無機亜鉛化合物、酢酸亜
鉛、シュウ酸亜鉛、クエン酸亜鉛、フマル酸亜鉛、ギ酸
亜鉛等の有機亜鉛塩が使用出来るが、特に好ましいもの
は亜鉛華(酸化亜鉛)及び炭酸亜鉛である。The individual deodorizing components used in the present invention are all known compounds, and the zinc compounds include various zinc compounds, such as zinc oxide, zinc sulfate, zinc chloride, zinc phosphate, zinc nitrate, and zinc carbonate. Inorganic zinc compounds such as zinc acetate, zinc oxalate, zinc citrate, zinc fumarate, zinc formate and other organic zinc salts can be used, and particularly preferred are zinc white (zinc oxide) and zinc carbonate.
本発明で使用する有機酸とは、脂肪族酸、芳香族酸及び
ポリマー酸が挙げられる。The organic acids used in the present invention include aliphatic acids, aromatic acids, and polymeric acids.
脂肪族酸として好ましいのは脂肪族ポリカルボン酸であ
り、例えば、シュウ酸、マロン酸、コハク酸、グルタル
酸、アジピン酸、ピメリン酸、フマル酸、マレイン酸、
メチルマレイン醪、メチルフマル駿、イタコン駿、シト
ラコン酸、メサモノ駿、アセチレン酸、リンゴ駿、メチ
ルリンゴ酸、クエン酸、インクエン酸、酒石酸等のジ又
はトリカルボン酸又はそれらの塩であり、本発明におい
て特に好ましいものはクエン酸及びフマル酸である。Preferred aliphatic acids are aliphatic polycarboxylic acids, such as oxalic acid, malonic acid, succinic acid, glutaric acid, adipic acid, pimelic acid, fumaric acid, maleic acid,
Di- or tricarboxylic acids such as methyl maleic acid, methyl fumaric acid, itaconic acid, citraconic acid, mesamonic acid, acetylenic acid, malic acid, methylmalic acid, citric acid, incitric acid, tartaric acid, or salts thereof, and in the present invention, particularly Preferred are citric acid and fumaric acid.
芳香族酸として好ましいのは芳香族ポリカルボン酸であ
り、例えば、フタル酸、テレフタル酸、イソフタル酸、
トリメリット酸、1,2.3−ベンゼントリカルボン酸
、1,3.5−ベンゼントリカルボン酸、ピロメリット
酸、ベンゼンヘキサカルボン酸、ナフタレンジカルボン
酸、ナフタレントリカルボン酸、ナフタレンテトラカル
ボン酸、ジフェニルテトラカルボン酸、ジフェニルエー
テルテトラカルボン酸、アゾベンゼンテトラカルボン酸
等の芳香族ポリカルボン酸或いはそれらの無水物であり
、本発明において特に好ましい芳香族ポリカルボン酸は
、ベンゼントリカルボン酸、特にトリメリット酸である
。Preferred aromatic acids are aromatic polycarboxylic acids, such as phthalic acid, terephthalic acid, isophthalic acid,
Trimellitic acid, 1,2.3-benzenetricarboxylic acid, 1,3.5-benzenetricarboxylic acid, pyromellitic acid, benzenehexacarboxylic acid, naphthalene dicarboxylic acid, naphthalene tricarboxylic acid, naphthalenetetracarboxylic acid, diphenyltetracarboxylic acid , diphenyl ether tetracarboxylic acid, azobenzenetetracarboxylic acid, and their anhydrides, and a particularly preferred aromatic polycarboxylic acid in the present invention is benzenetricarboxylic acid, particularly trimellitic acid.
ポリマー酸としてはその分子中にスルホン酸基、カルボ
ン駿基、硫酸エステル基、燐酸エステル基、フェノール
性水酸基を有するものであり、例えば下言己のものを包
含する。Polymeric acids include those having a sulfonic acid group, a carboxylic acid group, a sulfuric acid ester group, a phosphoric acid ester group, and a phenolic hydroxyl group in the molecule, and include, for example, those mentioned below.
イ、カルボン酸基を有するポリマー クエン酸、酒石酸
、フタル酸等の多価カルボン酸と、エチレングリコール
、1.4ブタンジオール、ジエチレングリコール等の多
価アルコールとを酸過剰で反応させて得られる末端カル
ボキシル基ポリエステル;各種多価カルボン酸で変性し
た酸性セルロース誘導体;多価カルボン酸のビニルエー
テルエステルモノマー等の単独重合体または他の一般的
なモノマーとのランダム共重合体、ブロック共重合体、
グラフト共重合体等;アクリル酸またはメタクリル酸等
のモノマーの単独重合体または他の一般的なモノマーと
のランダム共重合体、ブロック共重合体、グラフト共重
合体等;無水マレイン酸、イタコン酸等のα、β−不飽
和とニルモノマー等の単独重合体または他の一般的なモ
ノマーとのランダム共重合体、ブロック共重合体、グラ
フト共重合体等;
ロ、スルホン酸基を有するポリマー
エチルセルロース酢酸水素硫酸水素フタル酸エステル、
セルロース酢酸水素硫酸水素フタル酸、エチルセルロー
ス水素スルホ安息香酸エステル、スルホンベンジルセル
ロース酢酸エステル、エチルスルホエチルセルロース酢
酸エステル等の如きセルロース誘導体;ポリビニルアル
コールまたはビニルアルコール共重合体のスルホン酸化
合物(例えば、0−スルホ安息香酸、スルホプロピオン
酸、スルホバレリック酸、スルホベンズアルデヒド、ス
ルホフタル酸等)によるスルホン酸変性ポリマー等;
ハ、水酸基を有するポリマー
その他スルホン酸やフェノール基を含有するモノマーの
単独重合体または他の一般的なモノマーとのランダム共
重合体、ブロック共重合体、グラフト共重合体等;
その他カルボキシル基またはスルホン酸基またはフェノ
ール基含有化合物による各種重合体の酸性変性物等が挙
げられる。B. Polymer having a carboxylic acid group Terminal carboxyl obtained by reacting a polycarboxylic acid such as citric acid, tartaric acid, or phthalic acid with a polyhydric alcohol such as ethylene glycol, 1.4-butanediol, or diethylene glycol in excess of acid. Base polyester; acidic cellulose derivatives modified with various polyvalent carboxylic acids; homopolymers such as vinyl ether ester monomers of polyvalent carboxylic acids, or random copolymers and block copolymers with other common monomers,
Graft copolymers, etc.; homopolymers of monomers such as acrylic acid or methacrylic acid, or random copolymers, block copolymers, graft copolymers, etc. with other common monomers; maleic anhydride, itaconic acid, etc. Random copolymers, block copolymers, graft copolymers, etc. of α,β-unsaturation and homopolymers such as nil monomers, block copolymers, graft copolymers, etc.; b. Polymers having sulfonic acid groups, ethyl cellulose hydrogen acetate hydrogen sulfate phthalate,
Cellulose derivatives such as cellulose hydrogen acetate hydrogen sulfate phthalate, ethyl cellulose hydrogen sulfobenzoate, sulfonebenzyl cellulose acetate, ethyl sulfoethyl cellulose acetate, etc.; sulfonic acid compounds of polyvinyl alcohol or vinyl alcohol copolymers (e.g., 0-sulfonate); benzoic acid, sulfopropionic acid, sulfovaleric acid, sulfobenzaldehyde, sulfophthalic acid, etc.); C. Polymers with hydroxyl groups and other homopolymers of monomers containing sulfonic acid or phenol groups or other general Random copolymers, block copolymers, graft copolymers, etc. with other monomers; and acidic modified products of various polymers with compounds containing carboxyl groups, sulfonic acid groups, or phenol groups.
特に好ましいものは、カルボン酸基を有するポリマーで
ある。Particularly preferred are polymers with carboxylic acid groups.
以上の如き亜鉛化合物と有機酸とからなる脱臭成分は、
それらの使用比率も重要であって、合計量を100重量
部とすれば、亜鉛化合物が10〜90重量部に対し、有
機酸が90〜10重量部の割合であり、この様な組み合
わせ及び配合比において、本発明の目的が最良に達成さ
れる。使用比率が上記範囲から外れると、脱臭効果が不
充分となるので好ましくない。The deodorizing component consisting of a zinc compound and an organic acid as described above is
Their usage ratio is also important, and if the total amount is 100 parts by weight, the ratio of the zinc compound is 10 to 90 parts by weight and the organic acid is 90 to 10 parts by weight. In this ratio, the objectives of the invention are best achieved. If the usage ratio is outside the above range, the deodorizing effect will be insufficient, which is not preferable.
本発明の顆粒状芳香脱臭剤は、上記の成分を混合し、こ
れに必要に応じて適当な樹脂液をバインダーとして混合
し、顆粒状に成形することによって得られる。The granular aromatic deodorizing agent of the present invention can be obtained by mixing the above-mentioned components, optionally adding a suitable resin liquid as a binder, and forming the mixture into granules.
使用するバインダーとしては、低融点の有機化合物、ワ
ックス或いは合成樹脂や天然樹脂の水溶液或いは有機溶
剤溶液が適当であり、特に低融点の有機化合物やワック
スは、後に乾燥を必要としないので好ましい。この様な
バインダーとしては、ステアリン酸、ラウリン酸、リノ
ール酸、ナフテン酸、2−エチルへキソイン酸、オクチ
ル酸等の中〜高級脂肪酸、これらの脂肪酸の亜鉛、カル
シウム、マグネシウム、アルミニウム、鉛、錫、リチウ
ム等の金属塩、ポリエチレンワックス、ポリプロピレン
ワックス、マイクロクリスタリンワックス、ポリエチレ
ングリコール、ヒドロキシステアリン酸エチレンビスア
ミド(K−3ワツクス)、モンタン酸ワックス、エチレ
ン−酢酸ビニル共重合体ワックス等が挙げられる。勿論
、これら以外の低融点有機化合物も使用出来る。その他
ポリビニルアルコール、ポリアクリル酸、カルボキシメ
チルセルロース等のポリマーバインダーも使用すること
が出来る。The binder used is suitably a low melting point organic compound, wax, or an aqueous or organic solvent solution of a synthetic resin or natural resin. Low melting point organic compounds and waxes are particularly preferred since they do not require subsequent drying. Such binders include medium to higher fatty acids such as stearic acid, lauric acid, linoleic acid, naphthenic acid, 2-ethylhexoic acid, and octylic acid, and zinc, calcium, magnesium, aluminum, lead, and tin of these fatty acids. , metal salts such as lithium, polyethylene wax, polypropylene wax, microcrystalline wax, polyethylene glycol, hydroxystearate ethylene bisamide (K-3 wax), montan acid wax, ethylene-vinyl acetate copolymer wax, and the like. Of course, low melting point organic compounds other than these can also be used. Other polymer binders such as polyvinyl alcohol, polyacrylic acid, and carboxymethyl cellulose can also be used.
以上の如きバインダーは前記の脱臭成分100重量部当
たり、約5〜100重量部の割合で使用するのが好まし
く、使用量が上記範囲より少ないと顆粒状脱臭剤を得る
ことが困難となり、又、上記範囲を超える使用量では、
脱臭成分の脱臭効果が妨げられる。It is preferable to use the binder as described above in a proportion of about 5 to 100 parts by weight per 100 parts by weight of the deodorizing component. If the amount used is less than the above range, it will be difficult to obtain a granular deodorizing agent. If the amount used exceeds the above range,
The deodorizing effect of the deodorizing component is hindered.
本発明の顆粒状芳香脱臭剤は上記の如き脱臭成分及び芳
香剤をバインダーと均一に混合し、加熱又は少量の液体
を加えて混合物を可塑化し、これを適当なサイズに顆粒
状に造粒することによって得られる。好ましい造粒機は
、適当なサイズの孔を有するスクリーンメツシュを有す
る押圧機である。得られる顆粒状芳香脱臭剤は、いずれ
の太きさでもよいが、−船釣には0.5〜5mmの直径
が好ましい。The granular aromatic deodorizer of the present invention is produced by uniformly mixing the deodorizing component and aromatic agent described above with a binder, plasticizing the mixture by heating or adding a small amount of liquid, and granulating it into granules of an appropriate size. obtained by A preferred granulator is a press having a screen mesh with appropriately sized holes. The resulting granular aromatic deodorizer may have any diameter, but a diameter of 0.5 to 5 mm is preferred for boat fishing.
本発明の顆粒状芳香脱臭剤は上記の成分を必須成分とす
るが、その他従来公知の樹脂用の各種添加剤、例えば、
着色剤、充填剤、体質顔料、可塑剤、安定剤、紫外線吸
収剤等は必要に応じて任意に配合し得る。The granular aromatic deodorizing agent of the present invention has the above-mentioned components as essential components, and various other conventionally known additives for resins, such as
Colorants, fillers, extender pigments, plasticizers, stabilizers, ultraviolet absorbers, etc. may be optionally blended as necessary.
本発明の顆粒状芳香脱臭剤は、上記成分を単に混合し押
出造粒方法等によっても得ることができ、得られる顆粒
状芳香脱臭剤の粒径は約0. 1〜5mm程度が好適で
あるが、用途によっては更に細か(でも粗くてもよい。The granular aromatic deodorizer of the present invention can also be obtained by simply mixing the above components and extrusion granulation, etc. The particle size of the granular aromatic deodorizer obtained is about 0. Approximately 1 to 5 mm is suitable, but it may be finer (but coarser) depending on the purpose.
(実施例)
次に実施例を挙げて本発明を更に具体的に説明する。尚
、文中、部又は%とあるのは特に断りの無い限り重量基
準である。(Example) Next, the present invention will be described in more detail with reference to Examples. In the text, parts or percentages are based on weight unless otherwise specified.
実施例1
重量比が10:3の炭酸亜鉛及びクエン酸からなる混合
物90部にマイクロカプセル化芳香剤シトラス10部、
青色顔料0.1部及びポリアクリル酸エステルエマルジ
ョン50部(固形分30%)を混合し、ミキサーで混合
後、乾燥して本発明の顆粒状芳香脱臭剤を得た。この顆
粒状芳香脱臭剤の脱臭性を調べたところ下記の如くであ
った。Example 1 10 parts of microencapsulated fragrance citrus in 90 parts of a mixture of zinc carbonate and citric acid in a weight ratio of 10:3,
0.1 part of blue pigment and 50 parts of polyacrylic acid ester emulsion (solid content 30%) were mixed in a mixer and dried to obtain a granular aromatic deodorizer of the present invention. The deodorizing properties of this granular aromatic deodorizer were investigated and the results were as follows.
ヱ2匹三ロm区駄
上記顆粒状芳香脱臭剤3gを300mf2の三角フラス
コに入れ、次いで350ppmのアンモニア水100m
J2を入れ、口をパラフィンでシールし、アンモニアを
完全にガス化させた。その後、25℃に保存し、一定時
間経過後のフラスコ内のアンモニアCppm)を北川式
検知管で測定した結果は下記の通りであった。Put 3g of the above granular aromatic deodorizer into a 300mf2 Erlenmeyer flask, then add 100ml of 350ppm ammonia water.
J2 was added, the mouth was sealed with paraffin, and the ammonia was completely gasified. Thereafter, the flask was stored at 25°C, and the ammonia (Cppm) in the flask after a certain period of time was measured using a Kitagawa detector tube.The results were as follows.
上旦遺 λ旦止 主旦遺
ブランク 250 250 250本x皿昂1
20 15 2
「 −の ・
上記顆粒状芳香脱臭剤3gを300mβの三角フラスコ
に入れ、次いで800ppmの硫化ナトリウム水溶液1
+nJ2及び1規定の硫酸0.1mβを入れ、口をパラ
フィンでシールし、硫化水素を完全にガス化させた。そ
の後、25℃に保存し、一定時間経過後のフラスコ内の
硫化水素(ppm)を北川式検知管で測定した結果は下
記の通りであった。Jodan-e λdan-stop Shudan-e blank 250 250 250 pieces x plate 1
20 15 2 "-Pour 3 g of the above granular aromatic deodorizer into a 300 mβ Erlenmeyer flask, then add 1 800 ppm aqueous sodium sulfide solution.
+nJ2 and 0.1 mβ of 1N sulfuric acid were added, the mouth was sealed with paraffin, and hydrogen sulfide was completely gasified. Thereafter, the flask was stored at 25°C, and after a certain period of time, the hydrogen sulfide (ppm) in the flask was measured using a Kitagawa detector tube.The results were as follows.
上旦且 2旦止 亘旦止
ブランク 155 155 155本X皿五
6 非検出 非検出実施例2〜3
下記の成分を使用し、他は実施例1と同様にして本発明
の顆粒状芳香脱臭剤を得、実施例1と同様にしてその性
能を測定したところ下記の通りであった。155 155 155 pieces x 5 plates
6 Non-detection Non-detection Examples 2 to 3 A granular aromatic deodorizer of the present invention was obtained using the following components and in the same manner as in Example 1, and its performance was measured in the same manner as in Example 1. It was as follows.
夾五丞l
酸化亜鉛及びフマル酸の8部2混合物 95部芳香剤フ
ローラル 5部黄色顔料
0.2部ポリ酢酸ビニルエマルジョ
ン(固形分30%)30部
ヱ2j三タ111誌駈
ブランク
本l■翁
上旦遠
主旦遺 主旦孜
ブランク
本光肌易
夾施■ユ
炭酸亜鉛及びトリメリット酸の5部5混合物20部
芳香剤森林浴 80部赤色顔料
0.5部ポリ酢酸ビニルエ
マルジョン(固形分30%)30部
非検出
非検出
ブランク 250
本X皿易 130
硫化j1ト1庫4拭駈
よ旦臆
1旦遺 旦旦止
ブランク 155 155 155杢立皿M
35 非検出 非検出実施例4
酸化亜鉛及びフマル酸の8部2混合物 95部芳香剤フ
ローラル 5部黄色顔料
0.2部上記混合物75部に対して
ヒドロキシステアリン酸エチレンビスアマイド(K−3
ワツクス)15部とエチレン−酢酸ビニル共重合体(フ
ローパック)5部を加え、他は実施例1と同様にして本
発明の顆粒状芳香脱臭剤を得た。このものも前記実施例
1と同様な脱臭効果を有していた。8 parts 2 parts mixture of zinc oxide and fumaric acid 95 parts fragrance floral 5 parts yellow pigment
0.2 parts polyvinyl acetate emulsion (solid content 30%) 30 parts 2J Santa 111 magazine blank book l 5 parts of mellitic acid 20 parts of a mixture of 5 parts Aromatic forest bathing 80 parts Red pigment 0.5 parts Polyvinyl acetate emulsion (solid content 30%) 30 parts Non-detection Non-detection Blank 250 bottles 155 155 155 heathered plate M
35 Non-detection Non-detection Example 4 8 parts 2 mixture of zinc oxide and fumaric acid 95 parts fragrance floral 5 parts yellow pigment
0.2 parts Hydroxystearate ethylene bisamide (K-3
A granular aromatic deodorizer of the present invention was obtained in the same manner as in Example 1, except that 15 parts of wax) and 5 parts of ethylene-vinyl acetate copolymer (Flow Pack) were added. This product also had the same deodorizing effect as Example 1.
実施例5
炭酸亜鉛及びトリメリット酸の5:5混合物20部
芳香剤森林浴 80部赤色顔料
0.5部上記混合物75部
に対してモンタン酸ワックス(OP−ワックス)15部
、金属石鹸(ステアリン酸亜鉛)5部及びエチレン−酢
酸ビニル共重合体(フローバック)5部を加え、他は実
施例1と同様にして本発明の顆粒状芳香脱臭剤を得た。Example 5 20 parts of a 5:5 mixture of zinc carbonate and trimellitic acid Aromatic forest bathing 80 parts Red pigment 0.5 parts Montanic acid wax (OP-wax) 15 parts, Metallic soap (stearic acid) 75 parts of the above mixture A granular aromatic deodorizer of the present invention was obtained in the same manner as in Example 1 except that 5 parts of zinc) and 5 parts of ethylene-vinyl acetate copolymer (flowback) were added.
このものも前記実施例1と同様な脱臭効果を有していた
。This product also had the same deodorizing effect as Example 1.
実施例&
重量比610:3の炭酸亜鉛及びクエン酸からなる混合
物90部にマイクロカプセル化芳香剤シトラス10部及
び青色顔料0.1部を加え、これを三井三池製作所製ヘ
ンシェルミキサーにて1゜500rpmで3分間混合後
、この混合物75部にヒドロキシステアリン酸エチレン
ビスアマイド(K−3ワツクス)15部と金属石鹸(ス
テアリン酸亜鉛)5部を加え、ヘンシェルミキサーで1
.50Orpmで回転させながら、DIDA5部を加え
、約3分間混合し、その後ヘンシェルミキサーを約90
℃に加熱し、回転を750rpmにして、ワックス組成
物が融解して全体がブロック状の固まった時点を終点と
し、生成物をヘンシェルミキサーから取り畠した。これ
を熱いうちに造粒機(不二パウダル製、エックベレッタ
ーEAKS−1型)に移し、スクリーンメツシュ2mm
にて押出造粒し、本発明の顆粒状芳香脱臭剤を得た。こ
のものも前記実施例1と同様な脱臭効果を有していた。Example & Add 10 parts of microencapsulated fragrance Citrus and 0.1 part of blue pigment to 90 parts of a mixture consisting of zinc carbonate and citric acid in a weight ratio of 610:3, and mix the mixture at 1° with a Mitsui Miike Henschel mixer. After mixing at 500 rpm for 3 minutes, 15 parts of hydroxystearate ethylene bisamide (K-3 wax) and 5 parts of metal soap (zinc stearate) were added to 75 parts of this mixture, and the mixture was mixed with a Henschel mixer for 1 hour.
.. While rotating at 50 rpm, add 5 parts of DIDA, mix for approximately 3 minutes, then turn the Henschel mixer at approximately 90 rpm.
℃, the rotation was set to 750 rpm, and the end point was when the wax composition melted and the whole solidified into a block shape, and the product was removed from the Henschel mixer. Transfer this to a granulator (Eckberetter EAKS-1 type, manufactured by Fuji Paudal) while it is hot, and make a screen mesh of 2 mm.
The mixture was extruded and granulated to obtain the granular aromatic deodorizing agent of the present invention. This product also had the same deodorizing effect as Example 1.
(効果)
以上の様に本発明によれば、脱臭剤を顆粒状に成形する
ことによって、脱臭剤の脱臭効果を失うことなく、香料
によってマスキング効果を発揮させることが出来る。(Effect) As described above, according to the present invention, by forming the deodorizing agent into granules, the masking effect can be exerted by the fragrance without losing the deodorizing effect of the deodorizing agent.
他1名1 other person
Claims (3)
なることを特徴とする顆粒状芳香脱臭剤。(1) A granular aromatic deodorizer characterized by forming a fragrance, a zinc compound, and an organic acid into granules.
機酸90〜10重量部からなる請求項1に記載の顆粒状
芳香脱臭剤。(2) The granular aromatic deodorizer according to claim 1, wherein the deodorizing component comprises 10 to 90 parts by weight of a zinc compound and 90 to 10 parts by weight of an organic acid.
請求項1に記載の顆粒状芳香脱臭剤。(3) The granular aromatic deodorizer according to claim 1, wherein the organic acid is an aliphatic or aromatic polycarboxylic acid.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2108763A JPH048366A (en) | 1990-04-26 | 1990-04-26 | Granular aromatic deodorant |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2108763A JPH048366A (en) | 1990-04-26 | 1990-04-26 | Granular aromatic deodorant |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH048366A true JPH048366A (en) | 1992-01-13 |
Family
ID=14492878
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2108763A Pending JPH048366A (en) | 1990-04-26 | 1990-04-26 | Granular aromatic deodorant |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH048366A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5430021A (en) * | 1994-03-18 | 1995-07-04 | Pharmavene, Inc. | Hydrophobic drug delivery systems |
JP2005082585A (en) * | 2003-09-11 | 2005-03-31 | Kao Corp | Highly volatile composite particle |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5299218A (en) * | 1976-02-17 | 1977-08-19 | Toshio Tooyama | Deodrant for excrementitious matter |
JPS6377452A (en) * | 1986-09-22 | 1988-04-07 | 東レ株式会社 | Aromatic deodorizing agent |
JPH01171556A (en) * | 1987-12-28 | 1989-07-06 | Sekisui Chem Co Ltd | Deodorizing aromatic agent |
JPH01198549A (en) * | 1988-02-03 | 1989-08-10 | Dainichiseika Color & Chem Mfg Co Ltd | Granular deodorant |
-
1990
- 1990-04-26 JP JP2108763A patent/JPH048366A/en active Pending
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5299218A (en) * | 1976-02-17 | 1977-08-19 | Toshio Tooyama | Deodrant for excrementitious matter |
JPS6377452A (en) * | 1986-09-22 | 1988-04-07 | 東レ株式会社 | Aromatic deodorizing agent |
JPH01171556A (en) * | 1987-12-28 | 1989-07-06 | Sekisui Chem Co Ltd | Deodorizing aromatic agent |
JPH01198549A (en) * | 1988-02-03 | 1989-08-10 | Dainichiseika Color & Chem Mfg Co Ltd | Granular deodorant |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5430021A (en) * | 1994-03-18 | 1995-07-04 | Pharmavene, Inc. | Hydrophobic drug delivery systems |
JP2005082585A (en) * | 2003-09-11 | 2005-03-31 | Kao Corp | Highly volatile composite particle |
JP4515063B2 (en) * | 2003-09-11 | 2010-07-28 | 花王株式会社 | High volatility composite particles |
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