JPH05123387A - Deodorant and its manufacture - Google Patents
Deodorant and its manufactureInfo
- Publication number
- JPH05123387A JPH05123387A JP3086629A JP8662991A JPH05123387A JP H05123387 A JPH05123387 A JP H05123387A JP 3086629 A JP3086629 A JP 3086629A JP 8662991 A JP8662991 A JP 8662991A JP H05123387 A JPH05123387 A JP H05123387A
- Authority
- JP
- Japan
- Prior art keywords
- extract
- tea
- deodorant
- added
- adsorbent
- 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.)
- Granted
Links
- 239000002781 deodorant agent Substances 0.000 title claims abstract description 39
- 238000004519 manufacturing process Methods 0.000 title claims description 5
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims abstract description 42
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 claims abstract description 33
- 241001122767 Theaceae Species 0.000 claims abstract description 28
- 239000011668 ascorbic acid Substances 0.000 claims abstract description 14
- 235000010323 ascorbic acid Nutrition 0.000 claims abstract description 14
- 229960005070 ascorbic acid Drugs 0.000 claims abstract description 14
- 238000001179 sorption measurement Methods 0.000 claims abstract description 11
- 235000013616 tea Nutrition 0.000 claims description 32
- 238000000034 method Methods 0.000 claims description 25
- 239000004480 active ingredient Substances 0.000 claims description 21
- 235000006468 Thea sinensis Nutrition 0.000 claims description 16
- 235000020333 oolong tea Nutrition 0.000 claims description 16
- 239000003463 adsorbent Substances 0.000 claims description 14
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 10
- 239000011347 resin Substances 0.000 claims description 8
- 229920005989 resin Polymers 0.000 claims description 8
- 238000001914 filtration Methods 0.000 claims description 5
- 230000002378 acidificating effect Effects 0.000 claims description 4
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 claims description 3
- 239000011975 tartaric acid Substances 0.000 claims description 3
- 235000002906 tartaric acid Nutrition 0.000 claims description 3
- IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 claims 1
- 239000000787 lecithin Substances 0.000 claims 1
- 229940067606 lecithin Drugs 0.000 claims 1
- 235000010445 lecithin Nutrition 0.000 claims 1
- 239000011259 mixed solution Substances 0.000 claims 1
- 230000001877 deodorizing effect Effects 0.000 abstract description 27
- 239000007788 liquid Substances 0.000 abstract description 17
- 238000000605 extraction Methods 0.000 abstract description 14
- 239000000463 material Substances 0.000 abstract description 4
- 238000010521 absorption reaction Methods 0.000 abstract description 3
- 239000002253 acid Substances 0.000 abstract description 2
- 239000003795 chemical substances by application Substances 0.000 abstract description 2
- 238000011084 recovery Methods 0.000 abstract 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 24
- 230000000052 comparative effect Effects 0.000 description 18
- 239000000126 substance Substances 0.000 description 18
- ADRVNXBAWSRFAJ-UHFFFAOYSA-N catechin Natural products OC1Cc2cc(O)cc(O)c2OC1c3ccc(O)c(O)c3 ADRVNXBAWSRFAJ-UHFFFAOYSA-N 0.000 description 13
- 235000005487 catechin Nutrition 0.000 description 13
- 235000019441 ethanol Nutrition 0.000 description 13
- GVJHHUAWPYXKBD-UHFFFAOYSA-N (±)-α-Tocopherol Chemical compound OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-UHFFFAOYSA-N 0.000 description 8
- 230000000694 effects Effects 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 150000001765 catechin Chemical class 0.000 description 7
- 238000012360 testing method Methods 0.000 description 7
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 6
- 229950001002 cianidanol Drugs 0.000 description 6
- 150000008442 polyphenolic compounds Chemical class 0.000 description 6
- 235000013824 polyphenols Nutrition 0.000 description 6
- PFTAWBLQPZVEMU-DZGCQCFKSA-N (+)-catechin Chemical compound C1([C@H]2OC3=CC(O)=CC(O)=C3C[C@@H]2O)=CC=C(O)C(O)=C1 PFTAWBLQPZVEMU-DZGCQCFKSA-N 0.000 description 5
- 235000009569 green tea Nutrition 0.000 description 5
- 238000006386 neutralization reaction Methods 0.000 description 5
- 229920001864 tannin Polymers 0.000 description 5
- 235000018553 tannin Nutrition 0.000 description 5
- 239000001648 tannin Substances 0.000 description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 description 4
- 244000269722 Thea sinensis Species 0.000 description 4
- XMOCLSLCDHWDHP-IUODEOHRSA-N epi-Gallocatechin Chemical compound C1([C@H]2OC3=CC(O)=CC(O)=C3C[C@H]2O)=CC(O)=C(O)C(O)=C1 XMOCLSLCDHWDHP-IUODEOHRSA-N 0.000 description 4
- 235000019225 fermented tea Nutrition 0.000 description 4
- 229930003935 flavonoid Natural products 0.000 description 4
- 235000017173 flavonoids Nutrition 0.000 description 4
- 150000002215 flavonoids Chemical class 0.000 description 4
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 4
- GVJHHUAWPYXKBD-IEOSBIPESA-N α-tocopherol Chemical compound OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-IEOSBIPESA-N 0.000 description 4
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 3
- XMOCLSLCDHWDHP-UHFFFAOYSA-N L-Epigallocatechin Natural products OC1CC2=C(O)C=C(O)C=C2OC1C1=CC(O)=C(O)C(O)=C1 XMOCLSLCDHWDHP-UHFFFAOYSA-N 0.000 description 3
- 229930003427 Vitamin E Natural products 0.000 description 3
- 150000001413 amino acids Chemical class 0.000 description 3
- 238000004332 deodorization Methods 0.000 description 3
- WIGCFUFOHFEKBI-UHFFFAOYSA-N gamma-tocopherol Natural products CC(C)CCCC(C)CCCC(C)CCCC1CCC2C(C)C(O)C(C)C(C)C2O1 WIGCFUFOHFEKBI-UHFFFAOYSA-N 0.000 description 3
- 229910000037 hydrogen sulfide Inorganic materials 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000003960 organic solvent Substances 0.000 description 3
- 238000000926 separation method Methods 0.000 description 3
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 3
- 235000017557 sodium bicarbonate Nutrition 0.000 description 3
- 229940088594 vitamin Drugs 0.000 description 3
- 229930003231 vitamin Natural products 0.000 description 3
- 235000013343 vitamin Nutrition 0.000 description 3
- 239000011782 vitamin Substances 0.000 description 3
- 235000019165 vitamin E Nutrition 0.000 description 3
- 239000011709 vitamin E Substances 0.000 description 3
- 229940046009 vitamin E Drugs 0.000 description 3
- JLPULHDHAOZNQI-ZTIMHPMXSA-N 1-hexadecanoyl-2-(9Z,12Z-octadecadienoyl)-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCC\C=C/C\C=C/CCCCC JLPULHDHAOZNQI-ZTIMHPMXSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- ZZZCUOFIHGPKAK-UHFFFAOYSA-N D-erythro-ascorbic acid Natural products OCC1OC(=O)C(O)=C1O ZZZCUOFIHGPKAK-UHFFFAOYSA-N 0.000 description 2
- 102000004190 Enzymes Human genes 0.000 description 2
- 108090000790 Enzymes Proteins 0.000 description 2
- 229930003268 Vitamin C Natural products 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 238000007259 addition reaction Methods 0.000 description 2
- 229910021529 ammonia Inorganic materials 0.000 description 2
- 235000009508 confectionery Nutrition 0.000 description 2
- 238000004042 decolorization Methods 0.000 description 2
- DZYNKLUGCOSVKS-UHFFFAOYSA-N epigallocatechin Natural products OC1Cc2cc(O)cc(O)c2OC1c3cc(O)c(O)c(O)c3 DZYNKLUGCOSVKS-UHFFFAOYSA-N 0.000 description 2
- 150000002632 lipids Chemical class 0.000 description 2
- 230000000873 masking effect Effects 0.000 description 2
- 239000012046 mixed solvent Substances 0.000 description 2
- 230000003472 neutralizing effect Effects 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 229940083466 soybean lecithin Drugs 0.000 description 2
- 229930003799 tocopherol Natural products 0.000 description 2
- 235000010384 tocopherol Nutrition 0.000 description 2
- 239000011732 tocopherol Substances 0.000 description 2
- 229960001295 tocopherol Drugs 0.000 description 2
- 235000019154 vitamin C Nutrition 0.000 description 2
- 239000011718 vitamin C Substances 0.000 description 2
- PFTAWBLQPZVEMU-ZFWWWQNUSA-N (+)-epicatechin Natural products C1([C@@H]2OC3=CC(O)=CC(O)=C3C[C@@H]2O)=CC=C(O)C(O)=C1 PFTAWBLQPZVEMU-ZFWWWQNUSA-N 0.000 description 1
- PFTAWBLQPZVEMU-UKRRQHHQSA-N (-)-epicatechin Chemical compound C1([C@H]2OC3=CC(O)=CC(O)=C3C[C@H]2O)=CC=C(O)C(O)=C1 PFTAWBLQPZVEMU-UKRRQHHQSA-N 0.000 description 1
- 235000012984 Aspalathus linearis Nutrition 0.000 description 1
- 240000006914 Aspalathus linearis Species 0.000 description 1
- 240000006439 Aspergillus oryzae Species 0.000 description 1
- 235000002247 Aspergillus oryzae Nutrition 0.000 description 1
- 235000019224 Camellia sinensis var Qingmao Nutrition 0.000 description 1
- 235000009024 Ceanothus sanguineus Nutrition 0.000 description 1
- 241000723438 Cercidiphyllum japonicum Species 0.000 description 1
- 244000223760 Cinnamomum zeylanicum Species 0.000 description 1
- 240000003553 Leptospermum scoparium Species 0.000 description 1
- 235000015459 Lycium barbarum Nutrition 0.000 description 1
- VCUFZILGIRCDQQ-KRWDZBQOSA-N N-[[(5S)-2-oxo-3-(2-oxo-3H-1,3-benzoxazol-6-yl)-1,3-oxazolidin-5-yl]methyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C1O[C@H](CN1C1=CC2=C(NC(O2)=O)C=C1)CNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F VCUFZILGIRCDQQ-KRWDZBQOSA-N 0.000 description 1
- FKRUMFFNBGSGGM-MIYUYXAISA-N Oolonghomobisflavan B Natural products O=C(O[C@H]1[C@H](c2cc(O)c(O)c(O)c2)Oc2c(Cc3c(O)c4c(O[C@@H]([C@H](OC(=O)c5cc(O)c(O)c(O)c5)C4)c4cc(O)c(O)c(O)c4)cc3O)c(O)cc(O)c2C1)c1cc(O)c(O)c(O)c1 FKRUMFFNBGSGGM-MIYUYXAISA-N 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- XJNDVCUPPHDQHB-UHFFFAOYSA-N [N].CN1C(=O)N(C)C(=O)C2=C1N=CN2C Chemical compound [N].CN1C(=O)N(C)C(=O)C2=C1N=CN2C XJNDVCUPPHDQHB-UHFFFAOYSA-N 0.000 description 1
- 238000007792 addition Methods 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 150000001447 alkali salts Chemical class 0.000 description 1
- 229940087168 alpha tocopherol Drugs 0.000 description 1
- 230000004075 alteration Effects 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 235000006708 antioxidants Nutrition 0.000 description 1
- 239000003125 aqueous solvent Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 235000020279 black tea Nutrition 0.000 description 1
- 239000004566 building material Substances 0.000 description 1
- 125000004403 catechin group Chemical group 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 235000017803 cinnamon Nutrition 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 229920002770 condensed tannin Polymers 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000006911 enzymatic reaction Methods 0.000 description 1
- LPTRNLNOHUVQMS-UHFFFAOYSA-N epicatechin Natural products Cc1cc(O)cc2OC(C(O)Cc12)c1ccc(O)c(O)c1 LPTRNLNOHUVQMS-UHFFFAOYSA-N 0.000 description 1
- 235000012734 epicatechin Nutrition 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- -1 ethyl alcohol Chemical compound 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000000855 fermentation Methods 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 229940094952 green tea extract Drugs 0.000 description 1
- 235000020688 green tea extract Nutrition 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229920001461 hydrolysable tannin Polymers 0.000 description 1
- 244000144972 livestock Species 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- BJFGFQSYHAXQPO-YUTGENNUSA-N oolong homobisflavan A Natural products O=C(O[C@@H]1[C@H](c2cc(O)c(O)c(O)c2)Oc2c(Cc3c(O)cc(O)c4c3O[C@@H]([C@H](OC(=O)c3cc(O)c(O)c(O)c3)C4)c3cc(O)c(O)c(O)c3)c(O)cc(O)c2C1)c1cc(O)c(O)c(O)c1 BJFGFQSYHAXQPO-YUTGENNUSA-N 0.000 description 1
- BJFGFQSYHAXQPO-UHFFFAOYSA-N oolonghomobisflavan a Chemical compound OC1=C(O)C(O)=CC(C2C(CC3=C(O)C=C(O)C(CC=4C=5OC(C(OC(=O)C=6C=C(O)C(O)=C(O)C=6)CC=5C(O)=CC=4O)C=4C=C(O)C(O)=C(O)C=4)=C3O2)OC(=O)C=2C=C(O)C(O)=C(O)C=2)=C1 BJFGFQSYHAXQPO-UHFFFAOYSA-N 0.000 description 1
- FKRUMFFNBGSGGM-UHFFFAOYSA-N oolonghomobisflavan b Chemical compound OC1=C(O)C(O)=CC(C2C(CC3=C(O)C(CC=4C=5OC(C(OC(=O)C=6C=C(O)C(O)=C(O)C=6)CC=5C(O)=CC=4O)C=4C=C(O)C(O)=C(O)C=4)=C(O)C=C3O2)OC(=O)C=2C=C(O)C(O)=C(O)C=2)=C1 FKRUMFFNBGSGGM-UHFFFAOYSA-N 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 235000020339 pu-erh tea Nutrition 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000006722 reduction reaction Methods 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
- 229910000162 sodium phosphate Inorganic materials 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 229940092665 tea leaf extract Drugs 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 229960000984 tocofersolan Drugs 0.000 description 1
- 238000005809 transesterification reaction Methods 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- 150000003722 vitamin derivatives Chemical class 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 238000004065 wastewater treatment Methods 0.000 description 1
- 239000002076 α-tocopherol Substances 0.000 description 1
- 235000004835 α-tocopherol Nutrition 0.000 description 1
Landscapes
- Disinfection, Sterilisation Or Deodorisation Of Air (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は茶葉の抽出物を有効成分
とする消臭剤に関するものであり、特に消臭特性が改善
された消臭剤ならびにその製造方法に関するものであ
る。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a deodorant containing a tea leaf extract as an active ingredient, and more particularly to a deodorant having improved deodorant properties and a method for producing the same.
【0002】[0002]
【従来の技術および発明が解決しようとする課題】従
来、消臭方法として様々な方法が知られているが、大別
すると、マスキング法、化学的脱臭法、物理的吸着法お
よび生物的脱臭法の4種に分けることができる。2. Description of the Related Art Conventionally, various methods have been known as deodorizing methods. They are roughly classified into a masking method, a chemical deodorizing method, a physical adsorption method and a biological deodorizing method. Can be divided into four types.
【0003】以上の4種の脱臭方法を消臭機構的に説明
すると、マスキング法は香料を用いる方法であり、化学
的脱臭法は、酸化、還元、中和、付加反応を利用した方
法である。更に物理的吸着法は、活性炭やシリカゲル等
の多孔性物質により匂いのもととなる物質を吸着除去す
る方法であり、また生物的脱臭法は微生物や酵素を用い
る脱臭法である。Explaining the above four kinds of deodorizing methods in terms of deodorizing mechanism, the masking method is a method using a fragrance, and the chemical deodorizing method is a method utilizing oxidation, reduction, neutralization and addition reaction. .. Further, the physical adsorption method is a method of adsorbing and removing a substance that is a source of odor with a porous substance such as activated carbon or silica gel, and the biological deodorizing method is a deodorizing method using microorganisms or enzymes.
【0004】ところで、近年、消臭剤として、茶樹を含
むツバキ科植物の抽出物を有効成分が注目されている
が、この茶抽出物の消臭作用は前記の消臭法の中では化
学的脱臭法に属するものと考えられ、主な消臭作用は、
ポリフェノール(カテキン、タンニン類)やフラボノイ
ドに起因するものと推定される。特に、フェノール基を
有する物質は多くの錯化合物を作る性質があり、硫化水
素、アミン類等と結合し易いことがよく知られている。
従来から茶抽出物を用いた消臭剤としては種々のものが
知られているが、その大部分は緑茶の有効成分を使用し
たものである。By the way, in recent years, as the deodorant, an active ingredient of an extract of theaceae plant containing tea trees has been attracting attention, and the deodorizing action of this tea extract is chemical in the above deodorant method. It is considered to belong to the deodorizing method, and the main deodorizing action is
It is presumed to be caused by polyphenols (catechin, tannins) and flavonoids. In particular, it is well known that a substance having a phenol group has a property of forming many complex compounds and easily binds to hydrogen sulfide, amines and the like.
Various deodorants using a tea extract have been conventionally known, but most of them are those using an active ingredient of green tea.
【0005】本発明は、従来知られている消臭剤にも増
して消臭効果にすぐれた消臭剤、ならびに製造工程上に
おいても効率的かつ経済的に有利な方法を提供すること
を目的とする。It is an object of the present invention to provide a deodorant having an excellent deodorizing effect as compared with conventionally known deodorants, and an efficient and economically advantageous method in the manufacturing process. And
【0006】[0006]
【課題を解決するための手段】すなわち、本発明による
消臭剤は、茶の抽出物に対してクエン酸および所望によ
りアスコルビン酸を複合的に含有させてなることを特徴
とするものである。That is, the deodorant according to the present invention is characterized in that a tea extract is combined with citric acid and optionally ascorbic acid.
【0007】さらに本発明による消臭剤の製造方法は、
茶を弱塩基性の抽出剤を用いて抽出処理し、得られた抽
出液にクエン酸ならびに所望によりアスコルビン酸を添
加して弱酸性の第1抽出液を調製し、次いで、前記第1
抽出液を吸着材に接触させることによって、第1抽出液
中の有効成分を前記吸着材に吸着させて、その残部から
なる第2抽出液を調製し、前記吸着済みの吸着材から前
記有効成分を脱着させて回収し、このようにして得られ
た脱着回収成分と前記第2抽出液とを混合して消臭剤と
することを特徴とするものである。Further, the method for producing a deodorant according to the present invention comprises:
The tea is subjected to extraction treatment with a weakly basic extractant, and citric acid and optionally ascorbic acid are added to the obtained extract to prepare a weakly acidic first extract, and then the first extract is prepared.
The active ingredient in the first extract is adsorbed on the adsorbent by bringing the extract into contact with the adsorbent to prepare a second extract consisting of the rest, and the active ingredient is extracted from the adsorbed adsorbent. Is desorbed and recovered, and the desorbed and recovered component thus obtained is mixed with the second extract to form a deodorant.
【0008】本発明による消臭剤においては、後述する
ように、茶の内でも特にウーロン茶を抽出原料とするこ
とによって消臭効果の向上を図ることができる。In the deodorant according to the present invention, as will be described later, it is possible to improve the deodorizing effect by using oolong tea as an extraction raw material among teas.
【0009】一般に、茶の種類を分類すると、非発酵茶
(緑茶類)と半発酵茶(ウーロン茶等の中国茶類)及び
発酵茶(紅茶類)の三種に大別されるが、この中で半発
酵茶は茶葉中の酵素により短期間で作られる弱発酵茶
(ウーロン茶)と、麹菌により長期間堆積して作られる
後発酵茶(プーアル茶等)に細分類される。以上の各種
茶類の中で、特に消臭に関与する有効成分としては、ポ
リフェノール(カテキン、タンニン類)やフラボノイド
などが挙げられる。本発明においては、これらの茶種の
すべてに適用可能であるが、有効成分の主たる消臭作用
としては、たとえば、フラボノイド、タンニン類のフ
ェノール基と−NHとの結合によるもの、フラボノイ
ド類のうち、下記の基Generally, the types of tea are classified into three types, non-fermented tea (green teas), semi-fermented teas (Chinese teas such as oolong tea) and fermented teas (black teas). Semi-fermented tea is subdivided into weakly fermented tea (oolong tea), which is produced in a short period of time by enzymes in the tea leaves, and post-fermented tea (puer tea, etc.) produced by long-term deposition by koji mold. Among the various teas mentioned above, polyphenols (catechins, tannins), flavonoids and the like are mentioned as active ingredients particularly involved in deodorization. In the present invention, although it is applicable to all of these tea species, the main deodorizing action of the active ingredient is, for example, flavonoids, those resulting from the binding of a phenol group of tannins with -NH, and flavonoids. , The following groups
【0010】[0010]
【化1】 の−SH、−NHとの縮合、重合、付加反応によるも
の、 アミノ酸の[Chemical 1] Of -SH, -NH by condensation, polymerization, addition reaction,
【0011】[0011]
【化2】 と−SH、−NHとの中和反応によるもの、 有機酸と−NHの中和反応によるもの、 糖類の悪臭物質の吸収、吸着、溶解作用、 タンニン類のエステル化、エステル交換反応、 等の化学的、物理的な作用が複合的に働いて、茶の消臭
効果が発揮されるものと推定される。[Chemical 2] And -SH, -NH neutralization reaction, organic acid and -NH neutralization reaction, sugar malodorous substance absorption, adsorption, dissolution action, tannin esterification, transesterification, etc. It is presumed that the deodorizing effect of tea is exerted by the combined action of chemical and physical actions.
【0012】さらに本発明者の知見によれば、茶種によ
って有効成分の含有組成が異なり、たとえば、ポリフェ
ノール類の有効成分の含有量において、下記表のような
差異がある。Further, according to the knowledge of the present inventor, the content composition of the active ingredient differs depending on the tea species, and for example, the content of the active ingredient of polyphenols has the following differences.
【0013】 (mg/g) 成分 緑茶 ウーロン茶 紅 茶 プーアル茶 Flavan3-01類 130.0 mg/g 69.7 56.7 8.5 Proanthocyanidin類 5.2 7.2 5.1 0.7 Hydrolysable tannin 類 13.0 18.2 25.8 5.3 Theasinensin類 − 1.4 12.6 − Theaflavin類 − 1.0 10.7 − 合計 148.3 87.5 99.9 14.5 また、化学反応に関与する物質としてアミノ酸類と抗酸
化性物性であるビタミン類(特にEとC)の含有量につ
いては、茶の種類によって次表のような差異がみられ
る。(Mg / g) Ingredient Green tea Oolong tea Red tea Pu'er tea Flavan3-01s 130.0 mg / g 69.7 56.7 8.5 Proanthocyanidins 5.2 7.2 5.1 0.7 Hydrolysable tannins 13.0 18.2 25.8 5.3 Theasinensins-1.4 12.6-Theaflavins-1.0 10.7 -Total 148.3 87.5 99.9 14.5 Regarding the content of amino acids and vitamins that have antioxidant properties (especially E and C) as substances involved in the chemical reaction, there are differences as shown in the following table depending on the type of tea. Be done.
【0014】 (乾物中%) 茶の種類 全窒素 全アミノ酸 ビタミンC ビタミンE 玉露 6.49% 5.15 186 mg/g 24 mg/g 緑 茶 上 5.48 5.25 484 35 下 4.68 2.88 312 56 上 4.24 3.98 32 42 ウーロン茶 下 3.92 0.77 52 − 上 4.04 1.18 57 − 包 種 茶 下 4.26 1.57 64 − (註)ビタミンEとしてはα−トコフェロールが多い。(% In dry matter) Tea type Total nitrogen Total amino acids Vitamin C Vitamin E Gyokuro 6.49% 5.15 186 mg / g 24 mg / g Green tea Top 5.48 5.25 484 35 Bottom 4.68 2.88 312 56 Top 4.24 3.98 32 42 Oolong tea Bottom 3.92 0.77 52 − Upper 4.04 1.18 57 − Wrapped under tea 4.26 1.57 64 − (Note) Vitamin E is mostly α-tocopherol.
【0015】更にウーロン茶の銘柄別の成分値を示すと
次表の通りである。Further, the component values of oolong tea for each brand are shown in the following table.
【0016】 (乾物中%) 品名 全窒素 カフェイン 可溶分 粗タンニン 遊離アミノ酸 武夷仏手 2.89% 2.59 40.8 12.93 544.8 mg/100g 黄金桂 3.43 2.34 39.0 16.03 1004.8 武夷肉桂 3.38 2.21 37.0 11.32 1501.5 次に、消臭効果に最も関係の深い成分であると考えられ
るカテキン類の含量値をウーロン茶の品種別に表わした
ものを示す。(% Dry matter) Product name Total nitrogen Caffeine Soluble content Crude tannin Free amino acid Wuyi Buddha 2.89% 2.59 40.8 12.93 544.8 mg / 100g Golden katsura 3.43 2.34 39.0 16.03 1004.8 Wuyi cinnamon 3.38 2.21 37.0 11.32 1501.5 The contents of catechins, which are considered to be the components most closely related to the odor effect, are shown for each oolong tea variety.
【0017】 (乾物中%) 品種 −ECG −EC −EGCG −EGC 合計 上 1.66 % 0.29 3.75 0.92 6.62 中 1.16 0.33 3.60 1.01 6.10 下 1 1.16 0.22 2.92 1.22 5.52 下 2 0.96 0.21 2.93 1.08 5.21 (註)−ECG =エピカテキンガレート −EC =エピカテキン −EGCG=エピガロカテキンガレート −EGC =エピガロカテキン 以上の4種類のカテキンが従来知られていた茶のカテキ
ン類であるが、最近ウーロン茶特有の新カテキン重合物
として次の2種のカテキンが同定されている。式(1)
はウーロンホモビスフラバンAであり、式(2)はウー
ロンホモビスフラバンBの化学構造式である。(% Of dry matter) Variety- ECG- EC- EGCG- EGC Total Top 1.66% 0.29 3.75 0.92 6.62 Mid 1.16 0.33 3.60 1.01 6.10 Bottom 1 1.16 0.22 2.92 1.22 5.52 Bottom 2 0.96 0.21 2.93 1.08 5.21 (Note) -ECG = Epicatechin gallate-EC = Epicatechin-EGCG = Epigallocatechin gallate-EGC = Epigallocatechin The above four catechins are tea catechins that have been conventionally known, but recently a new catechin polymer unique to oolong tea. The following two catechins have been identified as Formula (1)
Is oolong homobisflavan A, and formula (2) is a chemical structural formula of oolong homobisflavan B.
【0018】[0018]
【化3】 [Chemical 3]
【0019】[0019]
【化4】 本発明者は、上記のような各種の茶の成分組成の知見に
加えて、さらに茶抽出成分と他の添加成分との複合的な
組み合わせがもたらす消臭効果に関してさらに研究した
結果、茶抽出成分に対してクエン酸を別途含有させるこ
とによって、消臭効果が一層すぐれたものになることを
見出した。さらに、本発明者の知見によれば、弱塩基性
の抽出剤で茶の抽出液を得た後さらにこれを中和し弱酸
性にする工程とこの中和工程に際して上記クエン酸を添
加する方法を採用することによって消臭効果が向上する
という知見を得ている。さらにまた、本発明において
は、茶抽出成分を一旦吸着剤(特に多孔性吸着樹脂)に
吸着させてさらにこれを脱着回収する工程を複合的に採
用することによって消臭効果に悪影響を及ぼすことなく
有効成分の含有率を増大させることができることを見出
した。[Chemical 4] The present inventor, in addition to the knowledge of the component composition of various teas as described above, as a result of further research on the deodorizing effect brought about by the complex combination of the tea extract component and other additive components, the tea extract component On the other hand, it was found that the deodorizing effect is further improved by adding citric acid separately. Furthermore, according to the knowledge of the present inventor, a step of obtaining a tea extract with a weakly basic extractant and then neutralizing it to make it weakly acidic and a method of adding the citric acid during the neutralizing step It has been found that the deodorizing effect is improved by adopting Furthermore, in the present invention, the deodorizing effect is not adversely affected by the combined use of the step of once adsorbing the tea extract component on the adsorbent (particularly the porous adsorbent resin) and further desorbing and collecting the adsorbent. It has been found that the content of active ingredient can be increased.
【0020】本発明における抽出原料としては、茶の内
でも特にウーロン茶がすぐれた効果を発揮する上で好ま
しい。ウーロン茶は緑茶とは異なる成分組成を有し、特
にウーロン茶特有のカテキンが存在し、更には半醗酵過
程での酵素反応により、未知の有効成分の生成等が推察
され、これらの成分が複合されて消臭効果に影響を与え
ていることが考えられるが、本発明においては、上記の
ように、中和段階で添加するクエン酸(およびアスコル
ビン酸)が、抗酸化性物質であるカテキン類、アスコル
ビン酸(ビタミンC)、トコフェロール(ビタミンE)
などの有効成分との間で相乗効果を発揮して、消臭効果
を向上させることが認められる。Of the teas, oolong tea is particularly preferable as the extraction raw material in the present invention because of its excellent effect. Oolong tea has a different component composition from green tea, in particular there is catechin peculiar to oolong tea, and further, due to an enzymatic reaction in the semi-fermentation process, the formation of unknown active ingredients is inferred, and these ingredients are combined. Although it is considered that the deodorizing effect is affected, in the present invention, as described above, the citric acid (and ascorbic acid) added in the neutralization step is catechins and ascorbin which are antioxidants. Acid (vitamin C), tocopherol (vitamin E)
It is recognized that a synergistic effect is exhibited with the active ingredients such as to improve the deodorizing effect.
【0021】本発明による方法においては、まず、茶の
有効成分を弱塩基性に調製されたエチルアルコールなど
のアルコールや他の有機溶媒系抽出剤、または有機溶媒
と水系溶媒との混合溶媒からなる抽出剤により抽出す
る。弱塩基性にすることによって抽出効率が向上する
が、この場合に添加する弱塩基性塩類としては、たとえ
ば重炭酸ナトリウムやリン酸ナトリウムなどが用いられ
得る。抽出剤のpHとしては、7.0〜8.2程度が適
当である。また、抽出剤中には、保護物質として、大豆
レシチンなどの脂質成分を含有させることが、消臭効果
の効力を維持させる上において好ましい。この脂質成分
は、消臭作用成分、特にビタミン類の変質を防止し、し
たがって消臭効果の向上とその維持において有効であ
る。本発明においては、上記抽出工程を、たとえば攪拌
機付ジャケット式密閉型缶に茶葉を投入し、上記抽出剤
で加温しながら抽出を行うことができる。ただし、この
場合、カテキン類の他に脂溶性ビタミンであるトコフェ
ロールの抽出効率を増大するためには、水のエタノール
の混合溶媒を抽出剤として使用することが望ましい。In the method of the present invention, first, the active ingredient of tea is composed of a weakly basic alcohol such as ethyl alcohol, another organic solvent-based extractant, or a mixed solvent of an organic solvent and an aqueous solvent. Extract with an extractant. The extraction efficiency is improved by making it weakly basic. As the weakly basic salts added in this case, for example, sodium bicarbonate or sodium phosphate can be used. The pH of the extractant is preferably about 7.0 to 8.2. In addition, it is preferable that the extractant contains a lipid component such as soybean lecithin as a protective substance in order to maintain the effect of the deodorizing effect. This lipid component prevents alteration of deodorant components, especially vitamins, and is therefore effective in improving and maintaining the deodorant effect. In the present invention, the extraction step can be carried out, for example, by putting tea leaves in a jacketed closed can with a stirrer and heating with the extractant. However, in this case, in order to increase the extraction efficiency of tocopherol, which is a fat-soluble vitamin, in addition to catechins, it is desirable to use a mixed solvent of water and ethanol as an extractant.
【0022】抽出完了後、適宜、遠心分離法などにより
固液分離を行って、抽出液にクエン酸ならびに所望によ
りアスコルビン酸を添加して弱酸性の第1抽出液を調製
する。アスコルビン酸は茶抽出物中に含まれているので
別途添加する必要は必ずしもないが、ウーロン茶を使用
する場合は比較的その含有量が少ないので、アスコルビ
ン酸を別途添加することが好ましい。この場合の弱酸性
の範囲としては、pH5.5〜6.8程度が適当であ
る。また、上記のようなクエン酸ならびにアスコルビン
酸の添加は消臭効果の向上とともに消臭剤の色調を良好
なものに調整する上においても有効である。After completion of the extraction, solid-liquid separation is appropriately carried out by a centrifugal separation method or the like, and citric acid and optionally ascorbic acid are added to the extract to prepare a weakly acidic first extract. Since ascorbic acid is contained in the tea extract, it is not always necessary to add it separately, but when oolong tea is used, its content is relatively small, so it is preferable to add ascorbic acid separately. In this case, the range of weak acidity is preferably pH 5.5 to 6.8. Further, the addition of citric acid and ascorbic acid as described above is effective not only for improving the deodorizing effect but also for adjusting the color tone of the deodorant to a good one.
【0023】さらに上記のようにして得られた第1抽出
液を吸着材で処理することによって、第1抽出液中の有
効成分を吸着材に吸着させて、一方、その残部からなる
第2抽出液を調製する。この場合に使用する吸着材とし
ては、多孔性吸着樹脂を用いることが好ましい。この吸
着工程によってカテキンなどのポリフェノール類が効果
的に吸着される。Further, by treating the first extract obtained as described above with an adsorbent, the active ingredient in the first extract is adsorbed on the adsorbent, while the second extract consisting of the remaining part is adsorbed. Prepare the liquid. The adsorbent used in this case is preferably a porous adsorbent resin. By this adsorption step, polyphenols such as catechin are effectively adsorbed.
【0024】次に、吸着済みの吸着材をエチルアルコー
ルなどの有機溶媒により洗浄することによって吸着され
ている有効成分を脱着・溶出させて、溶媒成分を蒸発留
去することにより有効成分を回収する。Next, the adsorbed material that has been adsorbed is washed with an organic solvent such as ethyl alcohol to desorb and elute the adsorbed active ingredient, and the solvent ingredient is removed by evaporation to recover the active ingredient. ..
【0025】このようにして有効成分の含有率が高めら
れた濃縮物である脱着回収成分と前記第2抽出液とを混
合し、さらに必要に応じて、脱色、濾過、濃縮などの工
程を経ることによって本発明の消臭剤を得る。In this way, the desorbed and recovered component, which is a concentrate in which the content of the active ingredient is increased, and the second extract are mixed, and if necessary, the steps such as decolorization, filtration and concentration are performed. Thus, the deodorant of the present invention is obtained.
【0026】[0026]
【実施例】以下、本発明を実施例に基づいて説明する
が、本発明はこれら実施例の記載に限定されるものでは
ない。実施例1 試験用小型抽出缶に水10リットルおよび95%エチル
アルコール10kgを仕込み、60℃に加温し、これに炭
酸水素ナトリウム15gと大豆レシチン10gを添加し
混合し溶解させる。この溶液のpHは7.6〜8.2で
あり、この溶液中にウーロン茶葉500gを投入し、3
0分間抽出した後、25℃に急冷し、次いで遠心分離機
により固液分離を行う。得られた抽出液(これをA液と
いう)にアスコルビン酸約10gとクエン酸約3gを添
加して中和しpHを5.8〜6.2に下げて色調を調整
した後、水を添加して全体を15リットルとする。次い
でこの液を多孔性吸着樹脂(PH−20)のカラムに通
し、カテキン等の成分をこれに吸着させ、処理液約15
リットルを得た(この液をB液という)。EXAMPLES The present invention will be described below based on examples, but the present invention is not limited to the description of these examples. Example 1 A small test can was charged with 10 liters of water and 10 kg of 95% ethyl alcohol, heated to 60 ° C., and 15 g of sodium hydrogencarbonate and 10 g of soybean lecithin were added and mixed to dissolve them. The pH of this solution is 7.6 to 8.2, and 500 g of oolong tea leaves are added to this solution to
After extracting for 0 minutes, it is rapidly cooled to 25 ° C., and then solid-liquid separation is performed by a centrifuge. About 10 g of ascorbic acid and about 3 g of citric acid were added to the obtained extract (this is referred to as solution A) to neutralize it, lower the pH to 5.8 to 6.2 to adjust the color tone, and then add water. And make the whole 15 liters. Then, this solution is passed through a column of a porous adsorption resin (PH-20) to adsorb components such as catechin to this, and a treatment solution of about 15
1 liter was obtained (this liquid is called liquid B).
【0027】次に上記の多孔性吸着樹脂を15%エチル
アルコールで洗浄後、80%エチルアルコールを通し、
吸着されているカテキン等の成分を脱着し溶出させる。
このようにして得られたエチルアルコール処理液を蒸発
によりアルコール分を留去し、残渣濃縮液5リットルを
得てさらにこの濃縮液に先に得たB液に加え、水を添加
して全体を20リットルにしたのち、活性炭で脱色後、
濾過、濃縮を行い、所定の濃度に調整して消臭剤を得
た。実施例2 実施例1で得た抽出液(A液)にアスコルビン酸約10
gとクエン酸約2g、さらに酒石酸約1gを添加し、p
Hを5.8〜6.2に調整し、さらに安定剤としてホス
ピタンCを添加し、さらに水を加えて全体を15リット
ルにする。Next, after washing the above porous adsorption resin with 15% ethyl alcohol, 80% ethyl alcohol was passed through the resin.
The adsorbed components such as catechin are desorbed and eluted.
The ethyl alcohol-treated solution thus obtained was evaporated to distill off the alcohol content to obtain 5 liters of a concentrated solution of the residue, and to this concentrated solution, the solution B was added, and water was added to make the whole. After making 20 liters, decolorize with activated carbon,
The deodorant was obtained by filtering and concentrating and adjusting the concentration to a predetermined level. Example 2 About 10 parts of ascorbic acid was added to the extract (solution A) obtained in Example 1.
g, citric acid about 2 g, and tartaric acid about 1 g are added, and p
The H is adjusted to 5.8 to 6.2, hospitane C is further added as a stabilizer, and further water is added to make the whole 15 liters.
【0028】次いで、この液を活性炭で脱色後、濾過、
濃縮を行い、所定の濃度に調整して消臭剤を得た。実施例3 試験用小型抽出缶に水40リットルを入れ、70℃に加
温し、これに炭酸水素ナトリウム30gを添加し溶解さ
せる。この溶液のpHは8.0であり、この溶液にウー
ロン茶1kgを投入し、30分間抽出した後、25℃に急
冷し、次いで遠心分離機により固液分離を行う。得られ
た抽出液にアスコルビン酸約20gとクエン酸約5gを
添加して中和し、pHを6.0に下げ色調を調整した
後、さらに水を加えて70リットルとする。Next, after decolorizing this liquid with activated carbon, filtration,
After concentration, the concentration was adjusted to a predetermined value to obtain a deodorant. Example 3 40 liters of water was placed in a small test canister and heated to 70 ° C., and 30 g of sodium hydrogen carbonate was added to and dissolved therein. The pH of this solution is 8.0, and 1 kg of oolong tea is added to this solution, which is extracted for 30 minutes, rapidly cooled to 25 ° C., and then solid-liquid separated by a centrifuge. About 20 g of ascorbic acid and about 5 g of citric acid are added to the obtained extract for neutralization, the pH is lowered to 6.0 to adjust the color tone, and water is further added to make 70 liters.
【0029】次いでこの液を多孔性吸着樹脂(PH−2
0)のカラムに通し、ポリフェノール等を吸着させ、処
理液約60リットルを得た(この液をA液と称する)。Next, this liquid was added to a porous adsorption resin (PH-2
It was passed through the column of 0) to adsorb polyphenol and the like to obtain about 60 liters of the treatment liquid (this liquid is referred to as liquid A).
【0030】次に多孔性吸着樹脂を15%エチルアルコ
ールで洗浄後、80%エチルアルコールを通すことによ
りポリフェノール等を脱着溶出させる。このエチルアル
コール処理液は蒸発によりアルコール分を留去し、残渣
濃縮液10リットルを得、このものをさきに得たA液に
加え、加水して100リットルとした後、活性炭で脱色
後、濾過、濃縮を行い、所定の濃度に調整して消臭剤を
得た。比較試験 上記本発明の実施例により得られた消臭剤の消臭効果を
試験した。この比較試験においては、下記の表に記載し
た悪臭物質を用い、検知管により消臭率を測定した。比
較例としては、市販されている下記の緑茶抽出物を主要
成分とする消臭剤を使用した。Next, the porous adsorption resin is washed with 15% ethyl alcohol, and then 80% ethyl alcohol is passed through to desorb and elute polyphenol and the like. The ethyl alcohol-treated solution was evaporated to remove the alcohol content, to obtain 10 liters of the concentrated residue, which was added to the solution A obtained above and water was added to make 100 liters, followed by decolorization with activated carbon and filtration. Then, it was concentrated and adjusted to a predetermined concentration to obtain a deodorant. Comparative test The deodorant effect of the deodorant obtained by the above-mentioned examples of the present invention was tested. In this comparative test, the malodorous substances listed in the table below were used, and the deodorizing rate was measured with a detector tube. As a comparative example, a deodorant containing the following commercially available green tea extract as a main component was used.
【0031】比較例1:フレッシュシライマツ(白井松
新薬株式会社製) 比較例2:サンカアキン(三井農林株式会社製) 比較例3:サンフラボン(太陽化学株式会社製) また、試験用臭気物質としてはアンモニア、トリメチル
アミン、硫化水素、メチルメルカプタンの4物質を使用
した。Comparative Example 1: Fresh Shiramatsu (manufactured by Shiraimatsu Shinyaku Co., Ltd.) Comparative Example 2: Sankaakin (manufactured by Mitsui Norin Co., Ltd.) Comparative Example 3: Sanflavone (manufactured by Taiyo Kagaku Co., Ltd.) Also, as an odor substance for testing. Used four substances of ammonia, trimethylamine, hydrogen sulfide and methyl mercaptan.
【0032】試験装置としては、北川式検知管を用い、
減圧下において、2分から60分に亘る段階的な測定を
行うことにより残渣濃度を調べ、消臭率を求めた。結果
を表1〜4に示す。As the test device, a Kitagawa type detector tube is used.
The residue concentration was examined by performing a stepwise measurement from 2 minutes to 60 minutes under reduced pressure, and the deodorizing rate was obtained. The results are shown in Tables 1 to 4.
【0033】 表 1(アンモニアの消臭率) 経過時間 試料 2分 5分 10分 30分 60分 実施例1 79 82 95 98 99 実施例2 77 80 94 98 99 実施例3 75 80 96 98 99 比較例1 70 78 88 97 98 比較例2 72 76 85 96 98 比較例3 70 74 84 95 97 表 2(トリメチルアミンの消臭率) 経過時間 試料 2分 5分 10分 30分 60分 実施例1 81 92 95 97 99 実施例2 83 89 96 96 99 実施例3 85 90 97 98 99 比較例1 80 88 92 96 98 比較例2 78 86 90 95 97 比較例3 72 80 88 92 95 表 3(硫化水素の消臭率) 経過時間 試料 2分 5分 10分 30分 60分 実施例1 35 46 56 63 68 実施例2 38 43 58 59 60 実施例3 44 52 60 62 66 比較例1 10 12 13 14 16 比較例2 15 18 20 26 30 比較例3 16 20 22 28 32 表 4(メチルメルカプタンの消臭率) 経過時間 試料 2分 5分 10分 30分 60分 実施例1 75 81 90 97 98 実施例2 76 80 89 94 91 実施例3 80 85 92 95 97 比較例1 74 80 90 94 95 比較例2 78 82 90 94 95 比較例3 65 70 88 90 92 上記比較試験結果から明らかなように、本発明による消
臭剤は従来の茶抽出物を有効成分とする消臭剤と比較し
て消臭効果にすぐれるとともに、特に本発明の消臭剤
は、短時間の内に消臭効果が発現する傾向が見られる点
で即効性にもすぐれている。 Table 1 (Ammonia deodorizing rate) Elapsed time Sample 2 minutes 5 minutes 10 minutes 30 minutes 60 minutes Example 1 79 82 95 98 99 Example 2 77 80 94 98 99 Example 3 75 80 96 98 99 Comparison Example 1 70 78 88 97 98 Comparative Example 2 72 76 85 96 98 Comparative Example 3 70 74 84 95 97 Table 2 (Deodorization rate of trimethylamine) Elapsed time Sample 2 minutes 5 minutes 10 minutes 30 minutes 60 minutes Example 1 81 92 95 97 99 Example 2 83 89 96 96 99 Example 3 85 90 97 98 99 Comparative Example 1 80 88 92 96 98 Comparative Example 2 78 86 90 95 97 Comparative Example 3 72 80 88 92 95 Table 3 (Discharge of hydrogen sulfide Odor rate) Elapsed time Sample 2 minutes 5 minutes 10 minutes 30 minutes 60 minutes Example 1 35 46 56 63 68 Example 2 38 43 58 59 60 Example 3 44 52 60 62 66 Comparative Example 1 10 12 13 14 16 Comparative Example 2 15 18 20 26 30 Comparative Example 3 16 20 22 28 32 Table 4 (Deodorization rate of methyl mercaptan) Elapsed time Sample 2 minutes 5 minutes 10 minutes 30 minutes 60 minutes Example 1 75 81 90 97 98 Example 2 76 80 89 94 91 Example 3 80 85 92 95 97 Comparative Example 1 74 80 90 94 95 Comparative Example 2 78 82 90 94 95 Comparative Example 3 65 70 88 90 92 As is clear from the results of the above comparative tests, the deodorant according to the present invention is a deodorant containing a conventional tea extract as an active ingredient. The deodorant effect is superior to that of the agent, and in particular, the deodorant of the present invention is also excellent in immediate effect in that the deodorant effect tends to be exhibited within a short period of time.
【0034】本発明による消臭剤は、消臭特性にすぐれ
るとともに茶の抽出物を有効成分としているので、その
用途としては、ガム、キャンデーなどの菓子類や畜産加
工品、水産加工品等の食品用をはじめ、建材、繊維製
品、冷蔵庫用、自動車内装品、生理用品、排水処理等広
範囲に亘る消臭剤として有用である。Since the deodorant according to the present invention has excellent deodorant properties and contains tea extract as an active ingredient, it is used as a confectionery such as gum and candy, processed livestock products, and processed marine products. It is useful as a deodorant for a wide range of applications including food products, building materials, textile products, refrigerators, automobile interior parts, sanitary products, and wastewater treatment.
Claims (9)
よりアスコルビン酸を複合的に含有させてなることを特
徴とする消臭剤。1. A deodorant characterized by comprising citric acid and optionally ascorbic acid in a complex manner with respect to an extract of tea.
の消臭剤。2. The deodorant according to claim 1, which further contains tartaric acid.
載の消臭剤。3. The deodorant according to claim 1, wherein the tea is oolong tea.
し、 得られた抽出液にクエン酸ならびに所望によりアスコル
ビン酸を添加して弱酸性の第1抽出液を調製し、 次いで、前記第1抽出液を吸着材に接触させることによ
って、第1抽出液中の有効成分を前記吸着材に吸着させ
て、その残部からなる第2抽出液を調製し、 前記吸着済みの吸着材から前記有効成分を脱着させて回
収し、 このようにして得られた脱着回収成分と前記第2抽出液
とを混合して消臭剤とすることを特徴とする、消臭剤の
製造方法。4. Tea is extracted with a weakly basic extractant, and citric acid and optionally ascorbic acid are added to the resulting extract to prepare a weakly acidic first extract, By contacting the first extract with an adsorbent, the active ingredient in the first extract is adsorbed on the adsorbent to prepare a second extract consisting of the rest of the adsorbent, A method for producing a deodorant, which comprises desorbing and recovering the active ingredient, and mixing the desorbed and recovered component thus obtained with the second extract to obtain a deodorant.
求項4に記載の方法。5. The method according to claim 4, wherein lecithin is added to the first extract.
る、請求項4に記載の方法。6. The method according to claim 4, wherein tartaric acid is further added to the first extract.
載の方法。7. The method of claim 4, wherein the tea is oolong tea.
る、請求項4に記載の方法。8. The method according to claim 4, wherein a porous adsorption resin is used as the adsorbent.
合液を、さらに活性炭で脱色後、濾過する工程を含む、
請求項4に記載の方法。9. A step of filtering the mixed solution of the desorbed and recovered component and the second extract after further decolorizing with activated carbon,
The method of claim 4.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3086629A JP3001283B2 (en) | 1991-04-18 | 1991-04-18 | Deodorant and method for producing the same |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3086629A JP3001283B2 (en) | 1991-04-18 | 1991-04-18 | Deodorant and method for producing the same |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH05123387A true JPH05123387A (en) | 1993-05-21 |
JP3001283B2 JP3001283B2 (en) | 2000-01-24 |
Family
ID=13892323
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP3086629A Expired - Fee Related JP3001283B2 (en) | 1991-04-18 | 1991-04-18 | Deodorant and method for producing the same |
Country Status (1)
Country | Link |
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JP (1) | JP3001283B2 (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH11228325A (en) * | 1998-02-17 | 1999-08-24 | Hiromi Nishii | Liquid agent composition compounded with plant extract |
JP2000302634A (en) * | 1999-04-27 | 2000-10-31 | Ichimaru Pharcos Co Ltd | Cosmetic composition |
JP2001198200A (en) * | 2000-01-19 | 2001-07-24 | Kobayashi Pharmaceut Co Ltd | Composition for deodorizing menstrual odor |
JP2007111437A (en) * | 2005-10-24 | 2007-05-10 | Taiyo Kagaku Co Ltd | High functional filter and its manufacturing method |
JP2020156792A (en) * | 2019-03-27 | 2020-10-01 | 保土谷化学工業株式会社 | Deodorizer containing iron-polyphenol composite and deodorization method using the deodorizer |
-
1991
- 1991-04-18 JP JP3086629A patent/JP3001283B2/en not_active Expired - Fee Related
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH11228325A (en) * | 1998-02-17 | 1999-08-24 | Hiromi Nishii | Liquid agent composition compounded with plant extract |
JP2000302634A (en) * | 1999-04-27 | 2000-10-31 | Ichimaru Pharcos Co Ltd | Cosmetic composition |
JP2001198200A (en) * | 2000-01-19 | 2001-07-24 | Kobayashi Pharmaceut Co Ltd | Composition for deodorizing menstrual odor |
JP2007111437A (en) * | 2005-10-24 | 2007-05-10 | Taiyo Kagaku Co Ltd | High functional filter and its manufacturing method |
JP2020156792A (en) * | 2019-03-27 | 2020-10-01 | 保土谷化学工業株式会社 | Deodorizer containing iron-polyphenol composite and deodorization method using the deodorizer |
Also Published As
Publication number | Publication date |
---|---|
JP3001283B2 (en) | 2000-01-24 |
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