US20110212037A1 - Process for producing purified essential oil - Google Patents
Process for producing purified essential oil Download PDFInfo
- Publication number
- US20110212037A1 US20110212037A1 US13/127,763 US200913127763A US2011212037A1 US 20110212037 A1 US20110212037 A1 US 20110212037A1 US 200913127763 A US200913127763 A US 200913127763A US 2011212037 A1 US2011212037 A1 US 2011212037A1
- Authority
- US
- United States
- Prior art keywords
- oil
- essential oil
- active carbon
- purified
- producing
- 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.)
- Abandoned
Links
- 239000000341 volatile oil Substances 0.000 title claims abstract description 190
- 238000000034 method Methods 0.000 title claims abstract description 104
- 230000008569 process Effects 0.000 title claims abstract description 49
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 111
- 239000000796 flavoring agent Substances 0.000 claims abstract description 110
- 235000019634 flavors Nutrition 0.000 claims abstract description 108
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 97
- 239000000356 contaminant Substances 0.000 claims abstract description 75
- 239000003905 agrochemical Substances 0.000 claims abstract description 65
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 claims abstract description 38
- 239000000126 substance Substances 0.000 claims abstract description 30
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- 235000005074 zinc chloride Nutrition 0.000 claims abstract description 19
- LLEMOWNGBBNAJR-UHFFFAOYSA-N biphenyl-2-ol Chemical compound OC1=CC=CC=C1C1=CC=CC=C1 LLEMOWNGBBNAJR-UHFFFAOYSA-N 0.000 claims description 78
- 239000000203 mixture Substances 0.000 claims description 72
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- 239000004306 orthophenyl phenol Substances 0.000 claims description 39
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- FAPWYRCQGJNNSJ-UBKPKTQASA-L calcium D-pantothenic acid Chemical compound [Ca+2].OCC(C)(C)[C@@H](O)C(=O)NCCC([O-])=O.OCC(C)(C)[C@@H](O)C(=O)NCCC([O-])=O FAPWYRCQGJNNSJ-UBKPKTQASA-L 0.000 description 1
- MKJXYGKVIBWPFZ-UHFFFAOYSA-L calcium lactate Chemical compound [Ca+2].CC(O)C([O-])=O.CC(O)C([O-])=O MKJXYGKVIBWPFZ-UHFFFAOYSA-L 0.000 description 1
- 239000001527 calcium lactate Substances 0.000 description 1
- 229960002401 calcium lactate Drugs 0.000 description 1
- 235000011086 calcium lactate Nutrition 0.000 description 1
- 229960002079 calcium pantothenate Drugs 0.000 description 1
- 239000001506 calcium phosphate Substances 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 239000003729 cation exchange resin Substances 0.000 description 1
- 229940112822 chewing gum Drugs 0.000 description 1
- 235000019219 chocolate Nutrition 0.000 description 1
- 229940043350 citral Drugs 0.000 description 1
- 235000000484 citronellol Nutrition 0.000 description 1
- FDJOLVPMNUYSCM-WZHZPDAFSA-L cobalt(3+);[(2r,3s,4r,5s)-5-(5,6-dimethylbenzimidazol-1-yl)-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl] [(2r)-1-[3-[(1r,2r,3r,4z,7s,9z,12s,13s,14z,17s,18s,19r)-2,13,18-tris(2-amino-2-oxoethyl)-7,12,17-tris(3-amino-3-oxopropyl)-3,5,8,8,13,15,18,19-octamethyl-2 Chemical compound [Co+3].N#[C-].N([C@@H]([C@]1(C)[N-]\C([C@H]([C@@]1(CC(N)=O)C)CCC(N)=O)=C(\C)/C1=N/C([C@H]([C@@]1(CC(N)=O)C)CCC(N)=O)=C\C1=N\C([C@H](C1(C)C)CCC(N)=O)=C/1C)[C@@H]2CC(N)=O)=C\1[C@]2(C)CCC(=O)NC[C@@H](C)OP([O-])(=O)O[C@H]1[C@@H](O)[C@@H](N2C3=CC(C)=C(C)C=C3N=C2)O[C@@H]1CO FDJOLVPMNUYSCM-WZHZPDAFSA-L 0.000 description 1
- 235000016213 coffee Nutrition 0.000 description 1
- 235000013353 coffee beverage Nutrition 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 239000006071 cream Substances 0.000 description 1
- 238000012364 cultivation method Methods 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- NEFBYIFKOOEVPA-UHFFFAOYSA-K dicalcium phosphate Chemical compound [Ca+2].[Ca+2].[O-]P([O-])([O-])=O NEFBYIFKOOEVPA-UHFFFAOYSA-K 0.000 description 1
- 229940038472 dicalcium phosphate Drugs 0.000 description 1
- 229910000390 dicalcium phosphate Inorganic materials 0.000 description 1
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
- PXEDJBXQKAGXNJ-QTNFYWBSSA-L disodium L-glutamate Chemical compound [Na+].[Na+].[O-]C(=O)[C@@H](N)CCC([O-])=O PXEDJBXQKAGXNJ-QTNFYWBSSA-L 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000004862 elemi Substances 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- 239000000284 extract Substances 0.000 description 1
- ZNOLGFHPUIJIMJ-UHFFFAOYSA-N fenitrothion Chemical compound COP(=S)(OC)OC1=CC=C([N+]([O-])=O)C(C)=C1 ZNOLGFHPUIJIMJ-UHFFFAOYSA-N 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- WTEVQBCEXWBHNA-JXMROGBWSA-N geranial Chemical compound CC(C)=CCC\C(C)=C\C=O WTEVQBCEXWBHNA-JXMROGBWSA-N 0.000 description 1
- HIGQPQRQIQDZMP-UHFFFAOYSA-N geranil acetate Natural products CC(C)=CCCC(C)=CCOC(C)=O HIGQPQRQIQDZMP-UHFFFAOYSA-N 0.000 description 1
- HIGQPQRQIQDZMP-DHZHZOJOSA-N geranyl acetate Chemical compound CC(C)=CCC\C(C)=C\COC(C)=O HIGQPQRQIQDZMP-DHZHZOJOSA-N 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 229950002441 glucurolactone Drugs 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 229910001385 heavy metal Inorganic materials 0.000 description 1
- 235000012907 honey Nutrition 0.000 description 1
- 235000015243 ice cream Nutrition 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 230000001939 inductive effect Effects 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 238000000752 ionisation method Methods 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 229930007744 linalool Natural products 0.000 description 1
- UWKAYLJWKGQEPM-UHFFFAOYSA-N linalool acetate Natural products CC(C)=CCCC(C)(C=C)OC(C)=O UWKAYLJWKGQEPM-UHFFFAOYSA-N 0.000 description 1
- 229940040145 liniment Drugs 0.000 description 1
- 239000000865 liniment Substances 0.000 description 1
- 239000007937 lozenge Substances 0.000 description 1
- BJEPYKJPYRNKOW-UHFFFAOYSA-N malic acid Chemical compound OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 description 1
- MEBQXILRKZHVCX-UHFFFAOYSA-N methidathion Chemical compound COC1=NN(CSP(=S)(OC)OC)C(=O)S1 MEBQXILRKZHVCX-UHFFFAOYSA-N 0.000 description 1
- 229960001952 metrifonate Drugs 0.000 description 1
- 235000020124 milk-based beverage Nutrition 0.000 description 1
- 239000008368 mint flavor Substances 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- 229930003658 monoterpene Natural products 0.000 description 1
- 235000002577 monoterpenes Nutrition 0.000 description 1
- 235000005152 nicotinamide Nutrition 0.000 description 1
- 239000011570 nicotinamide Substances 0.000 description 1
- 235000001968 nicotinic acid Nutrition 0.000 description 1
- 229960003512 nicotinic acid Drugs 0.000 description 1
- 239000011664 nicotinic acid Substances 0.000 description 1
- 150000004045 organic chlorine compounds Chemical class 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 239000005373 porous glass Substances 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 239000001103 potassium chloride Substances 0.000 description 1
- 235000011164 potassium chloride Nutrition 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- FITIWKDOCAUBQD-UHFFFAOYSA-N prothiofos Chemical compound CCCSP(=S)(OCC)OC1=CC=C(Cl)C=C1Cl FITIWKDOCAUBQD-UHFFFAOYSA-N 0.000 description 1
- RADKZDMFGJYCBB-UHFFFAOYSA-N pyridoxal hydrochloride Natural products CC1=NC=C(CO)C(C=O)=C1O RADKZDMFGJYCBB-UHFFFAOYSA-N 0.000 description 1
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 235000019192 riboflavin Nutrition 0.000 description 1
- 229960002477 riboflavin Drugs 0.000 description 1
- 239000002151 riboflavin Substances 0.000 description 1
- 235000011888 snacks Nutrition 0.000 description 1
- 235000019812 sodium carboxymethyl cellulose Nutrition 0.000 description 1
- 229920001027 sodium carboxymethylcellulose Polymers 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- GCLGEJMYGQKIIW-UHFFFAOYSA-H sodium hexametaphosphate Chemical compound [Na]OP1(=O)OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])O1 GCLGEJMYGQKIIW-UHFFFAOYSA-H 0.000 description 1
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 238000001256 steam distillation Methods 0.000 description 1
- 230000001954 sterilising effect Effects 0.000 description 1
- 238000004659 sterilization and disinfection Methods 0.000 description 1
- UVGUPMLLGBCFEJ-SWTLDUCYSA-N sucrose acetate isobutyrate Chemical compound CC(C)C(=O)O[C@H]1[C@H](OC(=O)C(C)C)[C@@H](COC(=O)C(C)C)O[C@@]1(COC(C)=O)O[C@@H]1[C@H](OC(=O)C(C)C)[C@@H](OC(=O)C(C)C)[C@H](OC(=O)C(C)C)[C@@H](COC(C)=O)O1 UVGUPMLLGBCFEJ-SWTLDUCYSA-N 0.000 description 1
- 238000000194 supercritical-fluid extraction Methods 0.000 description 1
- XOAAWQZATWQOTB-UHFFFAOYSA-N taurine Chemical compound NCCS(O)(=O)=O XOAAWQZATWQOTB-UHFFFAOYSA-N 0.000 description 1
- 235000007586 terpenes Nutrition 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- MYVIATVLJGTBFV-UHFFFAOYSA-M thiamine(1+) chloride Chemical compound [Cl-].CC1=C(CCO)SC=[N+]1CC1=CN=C(C)N=C1N MYVIATVLJGTBFV-UHFFFAOYSA-M 0.000 description 1
- 239000003053 toxin Substances 0.000 description 1
- 231100000765 toxin Toxicity 0.000 description 1
- 108700012359 toxins Proteins 0.000 description 1
- NFACJZMKEDPNKN-UHFFFAOYSA-N trichlorfon Chemical compound COP(=O)(OC)C(O)C(Cl)(Cl)Cl NFACJZMKEDPNKN-UHFFFAOYSA-N 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 235000019871 vegetable fat Nutrition 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 235000019163 vitamin B12 Nutrition 0.000 description 1
- 239000011715 vitamin B12 Substances 0.000 description 1
- 235000019158 vitamin B6 Nutrition 0.000 description 1
- 239000011726 vitamin B6 Substances 0.000 description 1
- 235000019154 vitamin C Nutrition 0.000 description 1
- 239000011718 vitamin C Substances 0.000 description 1
- 229940011671 vitamin b6 Drugs 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
- C11B9/00—Essential oils; Perfumes
- C11B9/02—Recovery or refining of essential oils from raw materials
- C11B9/022—Refining
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L2/00—Non-alcoholic beverages; Dry compositions or concentrates therefor; Their preparation
- A23L2/52—Adding ingredients
- A23L2/56—Flavouring or bittering agents
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L27/00—Spices; Flavouring agents or condiments; Artificial sweetening agents; Table salts; Dietetic salt substitutes; Preparation or treatment thereof
- A23L27/10—Natural spices, flavouring agents or condiments; Extracts thereof
- A23L27/12—Natural spices, flavouring agents or condiments; Extracts thereof from fruit, e.g. essential oils
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L27/00—Spices; Flavouring agents or condiments; Artificial sweetening agents; Table salts; Dietetic salt substitutes; Preparation or treatment thereof
- A23L27/10—Natural spices, flavouring agents or condiments; Extracts thereof
- A23L27/12—Natural spices, flavouring agents or condiments; Extracts thereof from fruit, e.g. essential oils
- A23L27/13—Natural spices, flavouring agents or condiments; Extracts thereof from fruit, e.g. essential oils from citrus fruits
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D15/00—Separating processes involving the treatment of liquids with solid sorbents; Apparatus therefor
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
- B01J20/02—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material
- B01J20/20—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material comprising free carbon; comprising carbon obtained by carbonising processes
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2002/00—Food compositions, function of food ingredients or processes for food or foodstuffs
Definitions
- the present invention relates to a process for producing a purified essential oil, a purified essential oil obtained by the process, a flavor composition comprising the purified essential oil, and food, drink, or oral care products, each comprising the purified essential oil and/or the flavor composition.
- the present invention relates to a process for producing a purified essential oil having excellent safety and high quality by efficiently removing a harmful contaminant such as residual agricultural chemicals contained in an essential oil without causing poor balance of flavor which the essential oil originally has, and decrease in flavor strength, a purified essential oil obtained by the process, a flavor composition comprising the purified essential oil, and food, drink, or oral care products, each comprising the purified essential oil and/or the flavor composition.
- Essential oil is an organic substance comprising a volatile odorant substance, extracted form a plant.
- the essential oil is obtained by treating a plant as a raw material with steam distillation, compression, extraction and the like, and recovering an oil comprising volatile odorant ingredients.
- citrus oil using citrus as a raw material is that monoterpene hydrocarbon which is a scent ingredient contained in citrus, and other terpene hydrocarbons are unstable to heat and light. For this reason, a so-called “cold press method” which recovers an oil by compressing citrus (particularly, coat of citrus) without applying heat is generally widely employed as a preparation method of the citrus oil.
- the essential oil obtained above is generally used without modification as flavor or fragrance in various uses including cosmetic or food.
- the essential oil is purified and used.
- a purification method in such a case, a method by distillation, a method of treating with a porous adsorbent, a cleaning treatment method, a filtration treatment method, and the like are employed.
- inorganic adsorbents such as active carbon, silica gel, alumina and zeolite
- organic adsorbents such as styrene-divinylbenzene copolymer adsorbent and acryl absorbent, ion-exchange resins, porous glasses, and the like are used (see Non-Patent Document 1).
- the essential oil is derived from natural plant, and should be inherently safe. However, a harmful contaminant such as agricultural chemicals, different from altered substances formed by chemical change and the like of the ingredients during storage and impurities originally contained in the essential oil, are sometimes detected, and the countermeasure becomes the problem.
- the cause that agricultural chemicals are detected from the essential oil includes the case where agricultural chemicals used in the course of growth of a plant or used in the course of storage and distribution of the plant harvested are attached to and adsorbed on the plant as a raw material, and the agricultural chemicals move into the essential oil and remain therein, and the case where a plant absorbs agricultural chemicals not decomposed and accumulated in the soil among agricultural chemicals used in the past, from root, and the agricultural chemicals move into the essential oil and remain therein.
- a method of conducting supercritical extraction of dried plant raw material, a method of conducting extraction treatment of a plant using a hydrophobic extractant, and the like are known as a method for producing a plant extract in which agricultural chemicals do not remain.
- those methods are a method that residual agricultural chemicals are avoided from being contained in a plant extract when preparing a plant extract by an extraction treatment of a plant. Therefore, the method cannot be applied to an essential oil, particularly citrus oil, in which scent ingredients are recovered by a compression method without using extraction.
- this method is a method for removing residual agricultural chemicals from a plant extract obtained by previously conducting an extraction treatment, such as a tea extract, and an essential oil obtained by compression without using extraction is not an intended material to be treated.
- Patent Document 2 A method of cleaning an essential oil with an alkaline aqueous solution (Patent Document 2) and a method of treating an essential oil with a strong ion-exchange resin (Patent Document 3) are known as the method for removing residual agricultural chemicals from an essential oil.
- the method of cleaning an essential oil with an alkaline aqueous solution has the problem that alkali-soluble flavor ingredients in the essential oil move into the alkaline aqueous solution, causing poor balance of flavor of the essential oil and considerable decrease in flavor strength, and the quality of the essential oil is greatly decreased.
- the method of treating an essential oil with a strong ion-exchange resin has various problems that (a) because the strong ion-exchange resin is hydrophilic while the essential oil is hydrophobic, it is difficult to increase contact efficiency of the essential oil to the strong ion-exchange resin, and removal efficiency of residual agricultural chemicals is low; (b) there is a concern that water incorporates into the essential oil; (c) there is a concern that aldehydes which are important flavor ingredients in the essential oil are ethanolated, thereby inducing a polymerization reaction; (d) in the case where the strong ion-exchange resin is a cationic ion-exchange resin, loss of acidic flavor compounds in the essential oil occurs, on the other hand, in the case where the strong ion-exchange resin is an anionic ion-exchange resin, loss of alkaline flavor compounds in the essential oil occurs, and poor balance of flavor of the essential oil and decrease in flavor strength are easy to occur; and (e) there is a concern that dissolution of
- Non-Patent Document 1 describes that in the case where coloration, precipitation, turbidity, deteriorated odor and the like occurred by chemical change and alternation of ingredients contained in the essential oil during storage, the essential oil is purified with an adsorbent such as active carbon, thereby improving flavor.
- Non-Patent Document 1 does not describe the preparation of an essential oil having excellent safety, free of contaminant such as agricultural chemicals by treating an essential oil contaminated with a contaminant such as agricultural chemicals with active carbon.
- Patent Document 1 JP-A-2000-72790
- Patent Document 2 WO 2007/117902
- Patent Document 3 WO 2007/001697
- Non-Patent Document 1 Journals of Patent Office, “Published collection of well-known prior arts (Flavor or Fragrance)”, Part 1, General of Flavor or Fragrance, Jan. 29, 1999, pages 4-5 and 72
- An object of the present invention is to provide a process for producing a purified essential oil, that can obtain a purified essential oil having excellent safety and high quality with high productivity by smoothly removing a contaminant from an essential oil comprising the contaminant such agricultural chemicals in a simple operation while maintaining good balance of flavor which the essential oil originally has and flavor strength without causing loss and deterioration of flavor ingredients contained in the essential oil.
- an object of the present invention is to provide a purified essential oil having excellent safety and quality, free of a contaminant such as agricultural chemicals and having good balance of flavor and high flavor strength.
- an object of the present invention is to provide a flavor composition comprising the purified essential oil having excellent safety and quality, products such as a food, drink, or oral care products, each comprising the purified essential oil and/or the flavor composition.
- the present inventors have made various investigations to achieve the above objects. As a result, they have found that when an essential oil comprising a contaminant is treated with an active carbon, the contaminant contained in the essential oil can be efficiently removed in an extremely simple operation while preventing poor balance of flavor and decrease in flavor strength, and a purified essential oil having excellent safety and quality can be produced with high productivity.
- the present inventors have further found that the method for removing a contaminants contained in an essential oil by the active carbon is very effective to the removal of residual agricultural chemicals from the essential oil.
- the method for removing a contaminant by treating the essential oil with an active carbon is also effective to any essential oil such as citrus oil, spice oil and herb oil, and above all, the method is more effective to the removal of a contaminant, particularly residual agricultural chemicals, contained in citrus oil.
- the present inventors have further found that in removing a contaminant contained in an essential oil with an active carbon, a temperature range exceeding the coagulation temperature of the essential oil and in which volatilization of the essential oil is low can be employed, and above all, when active carbon treatment is conducted at low temperature of from ⁇ 30° C. to 5° C., the removal rate of a contaminant such as agricultural chemicals, contained in the essential oil is further improved.
- an activated active carbon is preferably used from the point of high removal rate of a contaminant, and of such activated active carbon, active carbon activated with a chemical, particularly active carbon activated with zinc chloride, exhibits higher removal rate of a contaminant, particularly residual agricultural chemicals, and is therefore more preferably used.
- active carbon activated with a chemical particularly active carbon activated with zinc chloride
- the present invention is as follows.
- a process for producing a purified essential oil wherein an essential oil comprising a contaminant is treated with an active carbon to remove the contaminant.
- a food or drink comprising the purified essential oil according to (12) and/or the flavor composition according to (13).
- An oral care product comprising the purified essential oil according to (12) and/or the flavor composition according to (13).
- a contaminant contained in an essential oil can be efficiently removed with active carbon in an extremely simple operation while preventing poor balance of flavor and decrease in flavor strength, and therefore, a purified essential oil having excellent safety and quality can be produced with high productivity.
- the process of the present invention is extremely effective to the removal of agricultural chemicals from an essential oil comprising the agricultural chemicals as a contaminant.
- the purified essential oil obtained in the present invention does not contain a harmful contaminant such as agricultural chemicals, or if contained, contains the harmful contaminant in an extremely slight amount to an extent of not impairing humans and animals, and therefore it is excellent in safety.
- the process of the present invention is effective to any essential oil such as citrus oil, spice oil and herb oil, and above all, the contaminant, particularly residual agricultural chemicals, contained in the citrus oil can be removed with high removal rate.
- the contaminant such as agricultural chemicals, contained in the essential oil can be removed with higher removal rate.
- the activated active carbon particularly, active carbon activated with a chemical
- active carbon activated with zinc chloride is used as the active carbon for removing a contaminant
- the contaminant particularly residual agricultural chemicals
- the present invention relates to a process for producing a purified essential oil, comprising treating an essential oil comprising a contaminant with an active carbon, thereby removing the contaminant.
- contaminant used in the present description means substances that do not correspond to substances constituting a plant itself which is a raw material of an essential oil and substances derived from the substances (for example, substances formed by chemical change and alternation of substances constituting a plant), and is a generic name of substances that are harmful to humans and animals or substances that have a concern to be harmful.
- the kind of the contaminant contained in the essential oil is not particularly limited.
- Representative examples of the contaminant include agricultural chemicals, heavy metals, fungi, and toxins derived from fungus. Of those, the present invention is suitable for the removal of agricultural chemicals from the essential oil in which the agricultural chemicals remain therein.
- the kind of agricultural chemicals contained in the essential oil is not particularly limited, and can be any agricultural chemicals so long as it is agricultural chemicals capable of being removed by the process of the present invention.
- the agricultural chemicals include ortho-phenyl phenol, chloroneb, simazine, carbaryl, chlorpyrifos, imazalil, thiabendazole, diphenyl, trichlorfon, fenitrothion, prothiofos and methidathion.
- the agricultural chemicals contained in the essential oil may be any one kind of those, or may be two or more kinds of those.
- the process of the present invention is effective to the removal of agricultural chemicals such as ortho-phenyl phenol, chloroneb, simazine, carbaryl, chlorpyrifos, imazalil, thiabendazole and diphenyl, the residual agricultural chemicals thereof becoming the problem in the citrus oil, from the citrus oil comprising those agricultural chemicals, and is particularly suitable to the removal of ortho-phenyl phenol from the citrus oil comprising the ortho-phenyl phenol as residual agricultural chemicals.
- agricultural chemicals such as ortho-phenyl phenol, chloroneb, simazine, carbaryl, chlorpyrifos, imazalil, thiabendazole and diphenyl
- the kind of the essential oil used in the process of the present invention is not particularly limited, and any essential oil can be used so long as it is an essential oil that can achieve the object of the present invention. Above all, one kind or a mixture of two or more kinds of citrus oil, spice oil and herb oil is preferably used.
- citrus oil examples include lemon oil, sweet orange oil, bitter orange oil, lime oil, grapefruit oil, bergamot oil, mandarin oil, Yuzu oil (Citrus junos oil) and Sudachi oil (Citrus sudachi oil).
- spice oil examples include allspice, anise oil, star anise oil, bitter almond oil, blackcurrant oil, cinnamon oil, clove oil, ginger oil, mustard oil and pepper oil.
- herb oil examples include sweet basil oil, celery oil, clary sage oil, eucalyptus oil, peppermint oil, mint oil and spearmint oil.
- the essential oil used in the present invention may consist of any one kind of the above-described oils, and may be a mixture of two or more kinds of those.
- the kind of a contaminant, particularly the kind of agricultural chemicals, contained in the essential oil, and the content of the contaminant vary depending on the kind of a plant which is a raw material of an essential oil, production area of a plant, cultivation method of plant, storage/distribution methods, a preparation method of an essential oil from a plant, and the like.
- a plant which is a raw material of an essential oil
- production area of a plant production area of a plant
- cultivation method of plant storage/distribution methods
- a preparation method of an essential oil from a plant and the like.
- ortho-phenol which is one kind of agricultural chemicals frequently remains in an amount of a range of from 0.01 to 70 ppm when measured with gas chromatograph/mass spectrometry-mass spectrometry (GC/MS-MS).
- GC/MS-MS gas chromatograph/mass spectrometry-mass spectrometry
- powdery active carbon for example, powdery active carbon, granular active carbon (crushed carbon, granulate carbon, pelletized carbon), spherical active carbon and fibrous active carbon can be used as the active carbon.
- the powdery active carbon and/or the granular active carbon are preferably used from the points that the removal effect of a contaminant from an essential oil is high, and handling property, adsorption efficiency and economical efficiency are excellent.
- the origin of the active carbon used in the process of the present invention is not particularly limited.
- active carbon produced using palm shell, woody material (sawdust, wood chip and the like), coal or petroleum can be used.
- the active carbon using palm shell or woody material as a raw material is preferably used from the viewpoints of safety and environmental pollution prevention when the purified essential oil is used in food uses.
- the active carbon used in the process of the present invention may be activated active carbon or may be non-activated active carbon.
- the activated active carbon shows high removal rate of a contaminant from the essential oil, and is therefore preferably used.
- Active carbon activated with a gas such as steam and active carbon activated with a chemical can be used as the activated active carbon.
- the active carbon activated with a chemical particularly, the active carbon activated with zinc chloride, shows higher removal rate of contaminant, particularly residual agricultural chemicals, from the essential oil, and is therefore preferably used.
- examples of the active carbon that can be used in the process of the present invention include “Kyouryoku Shirasagi”, “Seisei Shirasagi” and “Tokusei Shirasagi” (each is zinc chloride-activated powdery active carbon), manufactured by Japan EnviroChemicals, Ltd.; “Shirasagi A”, “Shirasagi M”, “Shirasagi C” and “Shirasagi P” (each is steam-activated powdery active carbon), manufactured by the same company; “Shirasagi WH 2 c” (steam-activated granular active carbon) manufactured by the same company; “Kuraray Coal GL” and “Kuraray Coal GW” (steam-activated active carbon: powdery and granular), manufactured by Kurary Chemical Co., Ltd.; “Taiko S”, “Taiko SG” and “Taiko SGP” (each is zinc chloride-activated powder active carbon), manufactured by Futamura Chemical
- a purified essential oil by removing a contaminant such as agricultural chemicals, contained in the essential oil with the active carbon
- the following methods can be employed: a method for recovering a purified essential oil by adding active carbon to an essential oil comprising a contaminant, followed by stirring for a given time, and then separating the active carbon (batch method); and a method for recovering a purified essential oil by passing an essential oil comprising a contaminant through a column filled with the active carbon, thereby adsorbing the contaminant on the column (column method).
- the active carbon is generally added in an amount of preferably 0.1% by mass or more, and more preferably from 0.5 to 20% by mass, based on the mass of the essential oil comprising a contaminant, although varying depending on the kind of the essential oil, the kind and the content of the contaminant in the essential oil, the kind of the active carbon, and the like.
- the active carbon is added in an amount of from 20 to 3,000 parts by mass, particularly from about 50 to 1,500 parts by mass, per 1 part by mass of the contaminant.
- flow down rate and the like of the essential oil in the active carbon-filled column are adjusted according to the kind of the essential oil, the kind and the content of the contaminant in the essential oil, the kind of the active carbon, the filling amount of the active carbon in the column, and the like, so that the contaminant in the essential oil is sufficiently removed.
- the treatment time by the active carbon is preferably from 10 minutes to 5 hours.
- the purified essential oil obtained by the removal treatment of the contaminant with the active carbon can be directly used in the respective uses, or as may be necessary, the edible solvent as used in the method ( ⁇ ) is added to the essential oil, and the resulting dilute liquid can be used in the respective uses.
- Examples of the edible solvent used in the method ( ⁇ ) include ethanol, water, glycerin, medium-chain triglyceride and vegetable fat or oil. One kind or two or more kinds of those can be used.
- the edible solvent used here may be used in the respective uses in the form of an edible solvent solution of the purified essential oil without separating from the purified essential oil after completion of the removal treatment of the contaminant with the active carbon, or may be distilled away from the purified essential oil by distillation under reduced pressure, or the like.
- non-edible solvent used in the method ( ⁇ ) examples include organic solvents such as hexane, ethyl acetate, acetone, butanol, propanol and methanol. One kind or two or more kinds of those solvents can be used.
- the non-edible solvent used here is distilled away by distillation under reduced pressure or the like after completion of the removal treatment of the contaminant with active carbon.
- the removal treatment is conducted in a range of a temperature that the temperature (liquid temperature) of an essential oil liquid comprising a contaminant or a diluted essential oil solution is higher than the coagulation point of the essential oil and volatilization of the essential oil is small, regardless as to whether the treatment is conducted by the batch method or the column method, and regardless as to whether the treatment is conducted by any one of the above ( ⁇ ) to ( ⁇ ).
- the treatment with active carbon is conducted at a temperature such that the temperature (liquid temperature) of the essential oil or the essential oil solution, comprising a contaminant is a range of from ⁇ 30° C. to 5° C., preferably from ⁇ 25° C. to 5° C., and particularly preferably from ⁇ 25° C. to 2° C.
- the temperature can be smoothly removed with higher removal rate.
- the purified essential oil obtained by the process of the present invention does not have poor balance of flavor and decrease in flavor strength, maintains flavor and flavor strength that the essential oil originally has, has excellent flavor, does not contain contaminant or if contained, contains an extremely slight amount to an extent of not impairing humans and animals. Therefore, the purified essential oil has excellent safety.
- the purified essential oil obtained by the process of the present invention may be used as a flavor material without any modification, or may be used in the form of a flavor composition by appropriately combining with the conventional other flavor materials.
- the kind and the blending ratio of the other flavor material in the combination are not particularly limited, and in response to the kind and the like of the purified essential oil obtained by the process of the present invention, other flavor materials adapting thereto can be appropriately selected and used.
- Various foods, drinks, and oral care products can be prepared using the purified essential oil obtained by the process of the present invention and/or a flavor composition obtained by blending the purified essential oil with the other flavor materials.
- the food or drink include drinks such as fruit juice drink, sports drink, carbonated drink, milk beverage, teas drink, alcoholic drinks and health drink; frozen sweets such as ice creams, sherbets and ice candies; favorite foods such as Japanese and western confectioneries, chewing gums, chocolates, breads, coffee and tea; foods or drinks such as various snacks; and candies, although not limiting thereto.
- the oral care products include dentifrice, dental rinse, gingival massage cream, local endermic liniment, lozenge and chewing gum.
- MS model name “Quatro micro GC”, manufactured by Micromass
- a 0 is the content (ppm) of ortho-phenyl phenol in an essential oil (citrus oil) before purification treatment
- a 1 is the content (ppm) of ortho-phenyl phenol in an essential oil (citrus oil) after purification treatment.
- Example 1 by using “Seisei Shirasagi” which is active carbon activated with zinc chloride, as the active carbon, the ortho-phenyl phenol was efficiently removed with higher removal rate.
- the contaminant in removing the contaminant (residual agricultural chemicals and the like) contained in the essential oil (grapefruit cold press oil) by treating with active carbon, the contaminant (residual agricultural chemicals) can be effectively removed at a temperature in a range of from ⁇ 25° C. to 40° C. Above all, it was found that when the treatment is conducted at a temperature of room temperature or lower, particularly from ⁇ 25° C. to 5° C., the removal rate of ortho-phenyl phenol (agricultural chemical) is improved, and particularly, the removal rate in a temperature range of from ⁇ 25° C. to 2° C. is high.
- Example 4 Ingredients of the grapefruit cold press oil in which ortho-phenyl phenol remained therein (oil before subjecting to the treatment with active carbon) used in Example 4 were analyzed (analysis of flavor ingredients) with GC/MS-MS by the method described above, and additionally, in Example 4 (1), components of:
- purified grapefruit cold press oil obtained by the treatment of adding zinc chloride-activated powdery active carbon (Seisei Shirasagi) in an amount of 8% by mass, followed by stirring at room temperature (25° C.) for 1 hour (hereinafter referred to as “purified grapefruit oil (A)”), and
- purified grapefruit cold press oil obtained by the treatment of adding zinc chloride-activated powdery active carbon (Seisei Shirasagi) in an amount of 8% by mass, followed by stirring at a temperature of ⁇ 25° C. for 1 hour (hereinafter referred to as “purified grapefruit oil (B)”),
- C 0 is the content (ppm) of each ingredient in the essential oil (grapefruit oil) before subjecting to purification treatment
- C 1 is the content (ppm) of each ingredient in the essential oil (purified grapefruit oil) after conducting purification treatment.
- purified citrus oil obtained by treating the citrus oil (grapefruit cold press oil) in which agricultural chemical (ortho-phenyl phenol) remained therein with silica gel
- the residual ratio of nootkatone was extremely low, and almost all of nootkatone was lost.
- octanal, nonanal and decanal were lost in considerable amounts, causing poor balance of flavor, and decrease of flavor strength.
- fruit juice drink was prepared by using the ingredients shown in Table 4 below in amounts of the formulation shown in Table 4, uniformly mixing at 25° C., and then cooling to 5° C. The drink obtained had good orange flavor.
- carbonated drink was prepared by using the ingredients shown in Table 6 below in amounts of the formulation shown in Table 6, uniformly mixing at 15° C. under pressure, and then cooling to 5° C.
- the carbonated drink thus obtained had good taste and aroma since carboxylic acid was matched up with lemon flavor.
- health drink was prepared by using the ingredients shown in Table 7 below in amounts of the formulation shown in Table 7, uniformly mixing at 25° C., and then cooling to 5° C. The health drink thus obtained had good grapefruit flavor.
- dentifrice was prepared by using the ingredients shown in Table 8 below in amounts of the formulation shown in Table 8, uniformly mixing at 25° C., and then cooling to room temperature. The dentifrice thus obtained had lemon flavor.
- dental rinse was prepared by using the ingredients shown in Table 9 below in amounts of the formulation shown in Table 9, uniformly mixing at 25° C., and then cooling to 5° C.
- the dental rinse thus obtained had orange flavor.
- candy was manufactured by using the ingredients shown in Table 10 below in amounts of the formulation shown in Table 10, melt kneading at 100° C., extruding into a rod shape having a diameter of about 1.5 cm, solidifying by cooling, and then cutting to a given length (about 2 cm).
- the candy thus obtained had grapefruit flavor, had good aroma and good taste.
- sucrose acetate isobutylate (“SAM”, manufactured by Eastman Kodak Company), 1.67 g of the orange flavor composition prepared in Example 6, 3.33 g of middle-chain triglyceride (MCT OIL) (“PANACET 810”, manufactured by Ougi Chemical Co., Ltd.) and 0.2 g of an elemi resin were placed in a 200 ml beaker, and dissolved by heating, thereby obtaining a mixture comprising the orange flavor composition.
- SAM sucrose acetate isobutylate
- MCT OIL middle-chain triglyceride
- PANACET 810 manufactured by Ougi Chemical Co., Ltd.
- fruit juice drink was prepared by using the ingredients shown in Table 11 below in amounts of the formulation shown in Table 11, uniformly mixing at 25° C., and then cooling to 5° C.
- the drink thus obtained had orange flavor, and maintained high appearance of preference property.
- Citrus flavor composition was prepared by using the ingredients shown in Table 12 in the formulation shown in Table 12, and uniformly mixing at 25° C.
- the present invention is extremely useful as a process for producing a purified essential oil having excellent safety and high quality.
Abstract
It is provided a process for producing a purified essential oil excellent in safety and quality with high productivity from an essential oil comprising a harmful contaminant such as an agricultural chemical by simply and smoothly removing the contaminant with high removal rate without causing poor balance of flavor which the essential oil originally has, decrease of flavor strength and the like. It relates to a process for producing a purified essential oil by treating an essential oil comprising a contaminant with an active carbon to remove the contaminant and the removal rate of the contaminant is further improved by using an active carbon activated with a chemical, particularly an active carbon activated with zinc chloride, in the treatment, or by conducting the treatment at a low temperature of room temperature or lower, particularly at −25° C. to 5° C.
Description
- The present invention relates to a process for producing a purified essential oil, a purified essential oil obtained by the process, a flavor composition comprising the purified essential oil, and food, drink, or oral care products, each comprising the purified essential oil and/or the flavor composition.
- In more detail, the present invention relates to a process for producing a purified essential oil having excellent safety and high quality by efficiently removing a harmful contaminant such as residual agricultural chemicals contained in an essential oil without causing poor balance of flavor which the essential oil originally has, and decrease in flavor strength, a purified essential oil obtained by the process, a flavor composition comprising the purified essential oil, and food, drink, or oral care products, each comprising the purified essential oil and/or the flavor composition.
- Essential oil (essential oil or natural essential oil) is an organic substance comprising a volatile odorant substance, extracted form a plant. The essential oil is obtained by treating a plant as a raw material with steam distillation, compression, extraction and the like, and recovering an oil comprising volatile odorant ingredients.
- Of essential oils, citrus oil using citrus as a raw material is that monoterpene hydrocarbon which is a scent ingredient contained in citrus, and other terpene hydrocarbons are unstable to heat and light. For this reason, a so-called “cold press method” which recovers an oil by compressing citrus (particularly, coat of citrus) without applying heat is generally widely employed as a preparation method of the citrus oil.
- The essential oil obtained above is generally used without modification as flavor or fragrance in various uses including cosmetic or food. However, in the case where troubles such as coloration, precipitation, turbidity, deteriorated odor and the like occurred by chemical change and alternation of ingredients contained in the essential oil during storage, the essential oil is purified and used. As the purification method in such a case, a method by distillation, a method of treating with a porous adsorbent, a cleaning treatment method, a filtration treatment method, and the like are employed. In the case of treating with a porous adsorbent, inorganic adsorbents such as active carbon, silica gel, alumina and zeolite, organic adsorbents such as styrene-divinylbenzene copolymer adsorbent and acryl absorbent, ion-exchange resins, porous glasses, and the like are used (see Non-Patent Document 1).
- The essential oil is derived from natural plant, and should be inherently safe. However, a harmful contaminant such as agricultural chemicals, different from altered substances formed by chemical change and the like of the ingredients during storage and impurities originally contained in the essential oil, are sometimes detected, and the countermeasure becomes the problem.
- The cause that agricultural chemicals are detected from the essential oil includes the case where agricultural chemicals used in the course of growth of a plant or used in the course of storage and distribution of the plant harvested are attached to and adsorbed on the plant as a raw material, and the agricultural chemicals move into the essential oil and remain therein, and the case where a plant absorbs agricultural chemicals not decomposed and accumulated in the soil among agricultural chemicals used in the past, from root, and the agricultural chemicals move into the essential oil and remain therein.
- A method of conducting supercritical extraction of dried plant raw material, a method of conducting extraction treatment of a plant using a hydrophobic extractant, and the like are known as a method for producing a plant extract in which agricultural chemicals do not remain. However, those methods are a method that residual agricultural chemicals are avoided from being contained in a plant extract when preparing a plant extract by an extraction treatment of a plant. Therefore, the method cannot be applied to an essential oil, particularly citrus oil, in which scent ingredients are recovered by a compression method without using extraction.
- A method wherein a plant extract, in which organic chlorine compound type agricultural chemicals remain therein, is dissolved in a mixed solution of a lower aliphatic alcohol and water in a volume ratio of from 10:90 to 80:20, and then the resulting solution is contacted with a porous adsorbing resin having a modal radius of pores of from 30 to 120 angstroms, the porous adsorbing resin comprising a three-dimensional copolymer of styrene and divinylbenzene and the like, thereby adsorbing residual agricultural chemicals in the solution on the adsorbing resin, and the plant extract is recovered from the treated solution is known as a method for removing agricultural chemicals remained in a plant extract (Patent Document 1). However, in the case of this method, effective ingredients having similar properties to those of residual agricultural chemicals, contained in the plant extract are adsorbed on the absorbing resin together with the residual agricultural chemicals. As a result, there is a problem that absorption loss is large, resulting in decrease in yield of a plant extract.
- Furthermore, this method is a method for removing residual agricultural chemicals from a plant extract obtained by previously conducting an extraction treatment, such as a tea extract, and an essential oil obtained by compression without using extraction is not an intended material to be treated.
- A method of cleaning an essential oil with an alkaline aqueous solution (Patent Document 2) and a method of treating an essential oil with a strong ion-exchange resin (Patent Document 3) are known as the method for removing residual agricultural chemicals from an essential oil.
- However, the method of cleaning an essential oil with an alkaline aqueous solution has the problem that alkali-soluble flavor ingredients in the essential oil move into the alkaline aqueous solution, causing poor balance of flavor of the essential oil and considerable decrease in flavor strength, and the quality of the essential oil is greatly decreased.
- The method of treating an essential oil with a strong ion-exchange resin has various problems that (a) because the strong ion-exchange resin is hydrophilic while the essential oil is hydrophobic, it is difficult to increase contact efficiency of the essential oil to the strong ion-exchange resin, and removal efficiency of residual agricultural chemicals is low; (b) there is a concern that water incorporates into the essential oil; (c) there is a concern that aldehydes which are important flavor ingredients in the essential oil are ethanolated, thereby inducing a polymerization reaction; (d) in the case where the strong ion-exchange resin is a cationic ion-exchange resin, loss of acidic flavor compounds in the essential oil occurs, on the other hand, in the case where the strong ion-exchange resin is an anionic ion-exchange resin, loss of alkaline flavor compounds in the essential oil occurs, and poor balance of flavor of the essential oil and decrease in flavor strength are easy to occur; and (e) there is a concern that dissolution of the strong ion-exchange resin occurs by the essential oil.
- As described above, Non-Patent Document 1 describes that in the case where coloration, precipitation, turbidity, deteriorated odor and the like occurred by chemical change and alternation of ingredients contained in the essential oil during storage, the essential oil is purified with an adsorbent such as active carbon, thereby improving flavor. However, Non-Patent Document 1 does not describe the preparation of an essential oil having excellent safety, free of contaminant such as agricultural chemicals by treating an essential oil contaminated with a contaminant such as agricultural chemicals with active carbon.
- Under the above circumstances, development of a method capable of producing a purified essential oil having excellent safety and high quality with good productivity by smoothly removing a contaminant such as agricultural chemicals contained in the essential oil in a simple operation while maintaining good balance of flavor which an essential oil originally has and flavor strength without causing loss and deterioration of flavor ingredients contained in the essential oil is being demanded.
- Patent Document 1: JP-A-2000-72790
- Patent Document 2: WO 2007/117902
- Patent Document 3: WO 2007/001697
- Non-Patent Document 1: Journals of Patent Office, “Published collection of well-known prior arts (Flavor or Fragrance)”, Part 1, General of Flavor or Fragrance, Jan. 29, 1999, pages 4-5 and 72
- An object of the present invention is to provide a process for producing a purified essential oil, that can obtain a purified essential oil having excellent safety and high quality with high productivity by smoothly removing a contaminant from an essential oil comprising the contaminant such agricultural chemicals in a simple operation while maintaining good balance of flavor which the essential oil originally has and flavor strength without causing loss and deterioration of flavor ingredients contained in the essential oil.
- In addition, an object of the present invention is to provide a purified essential oil having excellent safety and quality, free of a contaminant such as agricultural chemicals and having good balance of flavor and high flavor strength.
- In addition, an object of the present invention is to provide a flavor composition comprising the purified essential oil having excellent safety and quality, products such as a food, drink, or oral care products, each comprising the purified essential oil and/or the flavor composition.
- The present inventors have made various investigations to achieve the above objects. As a result, they have found that when an essential oil comprising a contaminant is treated with an active carbon, the contaminant contained in the essential oil can be efficiently removed in an extremely simple operation while preventing poor balance of flavor and decrease in flavor strength, and a purified essential oil having excellent safety and quality can be produced with high productivity.
- The present inventors have further found that the method for removing a contaminants contained in an essential oil by the active carbon is very effective to the removal of residual agricultural chemicals from the essential oil.
- The present inventors have further found that the method for removing a contaminant by treating the essential oil with an active carbon is also effective to any essential oil such as citrus oil, spice oil and herb oil, and above all, the method is more effective to the removal of a contaminant, particularly residual agricultural chemicals, contained in citrus oil.
- The present inventors have further found that in removing a contaminant contained in an essential oil with an active carbon, a temperature range exceeding the coagulation temperature of the essential oil and in which volatilization of the essential oil is low can be employed, and above all, when active carbon treatment is conducted at low temperature of from −30° C. to 5° C., the removal rate of a contaminant such as agricultural chemicals, contained in the essential oil is further improved.
- The present inventors have further found that as the active carbon used in the removal of a contaminant contained in the essential oil, an activated active carbon is preferably used from the point of high removal rate of a contaminant, and of such activated active carbon, active carbon activated with a chemical, particularly active carbon activated with zinc chloride, exhibits higher removal rate of a contaminant, particularly residual agricultural chemicals, and is therefore more preferably used. The present invention has been completed based on those various findings.
- Specifically, the present invention is as follows.
- (1) A process for producing a purified essential oil, wherein an essential oil comprising a contaminant is treated with an active carbon to remove the contaminant.
- (2) The process for producing a purified essential oil according to (1), wherein the contaminant is a residual agricultural chemical.
- (3) The process for producing a purified essential oil according to (1) or (2), wherein the agricultural chemical is one kind or two or more kinds selected from ortho-phenyl phenol, chloroneb, simazine, carbaryl, chlorpyrifos, imazalil, thiabendazole and diphenyl.
- (4) The process for producing a purified essential oil according to any one of (1) to (3), wherein the essential oil is one kind or a mixture of two or more kinds selected from citrus oil, spice oil and herb oil
- (5) The process for producing a purified essential oil according to (4), wherein the citrus oil is one kind or a mixture of two or more kinds selected from lemon oil, sweet orange oil, bitter orange oil, lime oil, grapefruit oil, bergamot oil, mandarin oil, Yuzu oil (Citrus junos oil) and Sudachi oil (Citrus sudachi oil).
- (6) The process for producing a purified essential oil according to (4), wherein the spice oil is one kind or a mixture of two or more kinds selected from allspice, anise oil, star anise oil, bitter almond oil, blackcurrant oil, cinnamon oil, clove oil, ginger oil, mustard oil and pepper oil.
- (7) The process for producing a purified essential oil according to (4), wherein the herb oil is one kind or a mixture of two or more kinds selected from sweet basil oil, celery oil, clary sage oil, eucalyptus oil, peppermint oil, mint oil and spearmint oil.
- (8) The process for producing a purified essential oil according to any one of (1) to (7), wherein the essential oil is treated with the active carbon at a temperature of from −30° C. to 5° C.
- (9) The process for producing a purified essential oil according to any one of (1) to (8), wherein the active carbon is an activated active carbon.
- (10) The process for producing a purified essential oil according to (9), wherein the activated active carbon is an active carbon activated with a chemical.
- (11) The process for producing a purified essential oil according to (10), wherein the chemical is zinc chloride.
- (12) A purified essential oil obtained by the production process according to any one of (1) to (11).
- (13) A flavor composition comprising the purified essential oil according to (12).
- (14) A food or drink comprising the purified essential oil according to (12) and/or the flavor composition according to (13).
- (15) An oral care product comprising the purified essential oil according to (12) and/or the flavor composition according to (13).
- According to the process of the present invention, a contaminant contained in an essential oil can be efficiently removed with active carbon in an extremely simple operation while preventing poor balance of flavor and decrease in flavor strength, and therefore, a purified essential oil having excellent safety and quality can be produced with high productivity.
- In particular, the process of the present invention is extremely effective to the removal of agricultural chemicals from an essential oil comprising the agricultural chemicals as a contaminant. The purified essential oil obtained in the present invention does not contain a harmful contaminant such as agricultural chemicals, or if contained, contains the harmful contaminant in an extremely slight amount to an extent of not impairing humans and animals, and therefore it is excellent in safety.
- The process of the present invention is effective to any essential oil such as citrus oil, spice oil and herb oil, and above all, the contaminant, particularly residual agricultural chemicals, contained in the citrus oil can be removed with high removal rate.
- In the process of the present invention, when the treatment of an essential oil with an active carbon is conducted at low temperature, particularly from −30° C. to 5° C., the contaminant such as agricultural chemicals, contained in the essential oil can be removed with higher removal rate.
- In the process of the present invention, when the activated active carbon, particularly, active carbon activated with a chemical, above all, active carbon activated with zinc chloride, is used as the active carbon for removing a contaminant, the contaminant, particularly residual agricultural chemicals, can be extremely smoothly removed with further high removal rate.
- The present invention is described in detail below.
- The present invention relates to a process for producing a purified essential oil, comprising treating an essential oil comprising a contaminant with an active carbon, thereby removing the contaminant.
- The term “contaminant” used in the present description means substances that do not correspond to substances constituting a plant itself which is a raw material of an essential oil and substances derived from the substances (for example, substances formed by chemical change and alternation of substances constituting a plant), and is a generic name of substances that are harmful to humans and animals or substances that have a concern to be harmful.
- The kind of the contaminant contained in the essential oil is not particularly limited. Representative examples of the contaminant include agricultural chemicals, heavy metals, fungi, and toxins derived from fungus. Of those, the present invention is suitable for the removal of agricultural chemicals from the essential oil in which the agricultural chemicals remain therein.
- The kind of agricultural chemicals contained in the essential oil is not particularly limited, and can be any agricultural chemicals so long as it is agricultural chemicals capable of being removed by the process of the present invention. Examples of the agricultural chemicals include ortho-phenyl phenol, chloroneb, simazine, carbaryl, chlorpyrifos, imazalil, thiabendazole, diphenyl, trichlorfon, fenitrothion, prothiofos and methidathion. The agricultural chemicals contained in the essential oil may be any one kind of those, or may be two or more kinds of those.
- Of those, the process of the present invention is effective to the removal of agricultural chemicals such as ortho-phenyl phenol, chloroneb, simazine, carbaryl, chlorpyrifos, imazalil, thiabendazole and diphenyl, the residual agricultural chemicals thereof becoming the problem in the citrus oil, from the citrus oil comprising those agricultural chemicals, and is particularly suitable to the removal of ortho-phenyl phenol from the citrus oil comprising the ortho-phenyl phenol as residual agricultural chemicals.
- The kind of the essential oil used in the process of the present invention is not particularly limited, and any essential oil can be used so long as it is an essential oil that can achieve the object of the present invention. Above all, one kind or a mixture of two or more kinds of citrus oil, spice oil and herb oil is preferably used.
- More specifically, examples of the citrus oil include lemon oil, sweet orange oil, bitter orange oil, lime oil, grapefruit oil, bergamot oil, mandarin oil, Yuzu oil (Citrus junos oil) and Sudachi oil (Citrus sudachi oil).
- Examples of the spice oil include allspice, anise oil, star anise oil, bitter almond oil, blackcurrant oil, cinnamon oil, clove oil, ginger oil, mustard oil and pepper oil.
- Examples of the herb oil include sweet basil oil, celery oil, clary sage oil, eucalyptus oil, peppermint oil, mint oil and spearmint oil.
- The essential oil used in the present invention may consist of any one kind of the above-described oils, and may be a mixture of two or more kinds of those.
- The kind of a contaminant, particularly the kind of agricultural chemicals, contained in the essential oil, and the content of the contaminant vary depending on the kind of a plant which is a raw material of an essential oil, production area of a plant, cultivation method of plant, storage/distribution methods, a preparation method of an essential oil from a plant, and the like. For example, in the citrus oil obtained by a cold press method, ortho-phenol which is one kind of agricultural chemicals frequently remains in an amount of a range of from 0.01 to 70 ppm when measured with gas chromatograph/mass spectrometry-mass spectrometry (GC/MS-MS). The process of the present invention is extremely effective to the removal of ortho-phenyl phenol from citrus oil in which the ortho-phenyl phenol remains, obtained by the cold press method.
- In the process of the present invention, for example, powdery active carbon, granular active carbon (crushed carbon, granulate carbon, pelletized carbon), spherical active carbon and fibrous active carbon can be used as the active carbon. Of those, the powdery active carbon and/or the granular active carbon are preferably used from the points that the removal effect of a contaminant from an essential oil is high, and handling property, adsorption efficiency and economical efficiency are excellent.
- The origin of the active carbon used in the process of the present invention is not particularly limited. For example, active carbon produced using palm shell, woody material (sawdust, wood chip and the like), coal or petroleum can be used. Of those, the active carbon using palm shell or woody material as a raw material is preferably used from the viewpoints of safety and environmental pollution prevention when the purified essential oil is used in food uses.
- The active carbon used in the process of the present invention may be activated active carbon or may be non-activated active carbon. Of those, the activated active carbon shows high removal rate of a contaminant from the essential oil, and is therefore preferably used. Active carbon activated with a gas such as steam and active carbon activated with a chemical (zinc chloride, phosphoric acid or the like) can be used as the activated active carbon. Of those, the active carbon activated with a chemical, particularly, the active carbon activated with zinc chloride, shows higher removal rate of contaminant, particularly residual agricultural chemicals, from the essential oil, and is therefore preferably used.
- Although not limited, examples of the active carbon that can be used in the process of the present invention include “Kyouryoku Shirasagi”, “Seisei Shirasagi” and “Tokusei Shirasagi” (each is zinc chloride-activated powdery active carbon), manufactured by Japan EnviroChemicals, Ltd.; “Shirasagi A”, “Shirasagi M”, “Shirasagi C” and “Shirasagi P” (each is steam-activated powdery active carbon), manufactured by the same company; “Shirasagi WH2c” (steam-activated granular active carbon) manufactured by the same company; “Kuraray Coal GL” and “Kuraray Coal GW” (steam-activated active carbon: powdery and granular), manufactured by Kurary Chemical Co., Ltd.; “Taiko S”, “Taiko SG” and “Taiko SGP” (each is zinc chloride-activated powder active carbon), manufactured by Futamura Chemical Co., Ltd.; and “Diahope S80S”, manufactured by Calgon Mitsubishi Chemical Corporation.
- In producing a purified essential oil by removing a contaminant such as agricultural chemicals, contained in the essential oil with the active carbon, the following methods can be employed: a method for recovering a purified essential oil by adding active carbon to an essential oil comprising a contaminant, followed by stirring for a given time, and then separating the active carbon (batch method); and a method for recovering a purified essential oil by passing an essential oil comprising a contaminant through a column filled with the active carbon, thereby adsorbing the contaminant on the column (column method).
- In the case of producing the purified essential oil by the batch method, the active carbon is generally added in an amount of preferably 0.1% by mass or more, and more preferably from 0.5 to 20% by mass, based on the mass of the essential oil comprising a contaminant, although varying depending on the kind of the essential oil, the kind and the content of the contaminant in the essential oil, the kind of the active carbon, and the like. In the case where the content of the contaminant contained in the essential oil is the basis, it is preferred that the active carbon is added in an amount of from 20 to 3,000 parts by mass, particularly from about 50 to 1,500 parts by mass, per 1 part by mass of the contaminant.
- In the case of producing the purified essential oil by the column method, flow down rate and the like of the essential oil in the active carbon-filled column are adjusted according to the kind of the essential oil, the kind and the content of the contaminant in the essential oil, the kind of the active carbon, the filling amount of the active carbon in the column, and the like, so that the contaminant in the essential oil is sufficiently removed.
- In any of the batch method and the column method, the treatment time by the active carbon is preferably from 10 minutes to 5 hours.
- In removing the contaminant contained in the essential oil with the active carbon, the following methods can be employed. (α) A method of directly using the essential oil comprising the contaminant without diluting with a solvent and treating the same with the active carbon; (β) a method of mixing an edible solvent with the essential oil comprising the contaminant to dilute the essential oil, and treating the resulting dilute liquid with the active carbon; (γ) a method of adding a non-edible solvent to the essential oil comprising the contaminant to dilute the essential oil, and treating the resulting dilute liquid with the active carbon; and (δ) a method of diluting the essential oil comprising the contaminant with an essential oil free of a contaminant, and treating the resulting dilute liquid with the active carbon.
- In the case of employing the methods (α) and (δ), the purified essential oil obtained by the removal treatment of the contaminant with the active carbon can be directly used in the respective uses, or as may be necessary, the edible solvent as used in the method (β) is added to the essential oil, and the resulting dilute liquid can be used in the respective uses.
- Examples of the edible solvent used in the method (β) include ethanol, water, glycerin, medium-chain triglyceride and vegetable fat or oil. One kind or two or more kinds of those can be used. The edible solvent used here may be used in the respective uses in the form of an edible solvent solution of the purified essential oil without separating from the purified essential oil after completion of the removal treatment of the contaminant with the active carbon, or may be distilled away from the purified essential oil by distillation under reduced pressure, or the like.
- Examples of the non-edible solvent used in the method (γ) include organic solvents such as hexane, ethyl acetate, acetone, butanol, propanol and methanol. One kind or two or more kinds of those solvents can be used. The non-edible solvent used here is distilled away by distillation under reduced pressure or the like after completion of the removal treatment of the contaminant with active carbon.
- In removing the contaminant by treating the essential oil comprising a contaminant with active carbon, the removal treatment is conducted in a range of a temperature that the temperature (liquid temperature) of an essential oil liquid comprising a contaminant or a diluted essential oil solution is higher than the coagulation point of the essential oil and volatilization of the essential oil is small, regardless as to whether the treatment is conducted by the batch method or the column method, and regardless as to whether the treatment is conducted by any one of the above (α) to (δ). Above all, the treatment with active carbon is conducted at a temperature such that the temperature (liquid temperature) of the essential oil or the essential oil solution, comprising a contaminant is a range of from −30° C. to 5° C., preferably from −25° C. to 5° C., and particularly preferably from −25° C. to 2° C. By employing the temperature, the contaminant can be smoothly removed with higher removal rate.
- The purified essential oil obtained by the process of the present invention does not have poor balance of flavor and decrease in flavor strength, maintains flavor and flavor strength that the essential oil originally has, has excellent flavor, does not contain contaminant or if contained, contains an extremely slight amount to an extent of not impairing humans and animals. Therefore, the purified essential oil has excellent safety.
- The purified essential oil obtained by the process of the present invention may be used as a flavor material without any modification, or may be used in the form of a flavor composition by appropriately combining with the conventional other flavor materials. The kind and the blending ratio of the other flavor material in the combination are not particularly limited, and in response to the kind and the like of the purified essential oil obtained by the process of the present invention, other flavor materials adapting thereto can be appropriately selected and used.
- Various foods, drinks, and oral care products can be prepared using the purified essential oil obtained by the process of the present invention and/or a flavor composition obtained by blending the purified essential oil with the other flavor materials. Examples of the food or drink include drinks such as fruit juice drink, sports drink, carbonated drink, milk beverage, teas drink, alcoholic drinks and health drink; frozen sweets such as ice creams, sherbets and ice candies; favorite foods such as Japanese and western confectioneries, chewing gums, chocolates, breads, coffee and tea; foods or drinks such as various snacks; and candies, although not limiting thereto. Examples of the oral care products include dentifrice, dental rinse, gingival massage cream, local endermic liniment, lozenge and chewing gum.
- The present invention is described specifically below by Examples and the like, but it should be understood that the invention is not limited to the following Examples and the like.
- In the following Examples and Comparative Examples, quantitative determination of residual agricultural chemicals (ortho-phenyl phenol) in the essential oil (various citrus oils) and quantitative determination of each ingredient contained in the essential oil (each flavor ingredient) were conducted by gas chromatograph/mass spectrometry-mass spectroscopy (GC/MS-MS) employing the following apparatus and conditions.
- GC model name: “Agilent Technologies HP6890N”, manufactured by Agilent Technologies
- GC column name: “DB-5MS” (30 m×0.25 mm I.D., thickness: 0.25 μm), manufactured by Agilent Technologies
- MS model name: “Quatro micro GC”, manufactured by Micromass
- GC conditions
-
- Injection method: Splitless
- Injection amount: 2 μL
- Injection inlet temperature: 250° C.
- Column temperature: 50° C. for 1 minute→Heating to 125° C. at 15° C./min→Heating to 300° C. at 5° C./min, and then maintaining at 300° C. for 9 minutes
- Flow rate: 1.0 ml/min
- MS-MS conditions
-
- Ion source temperature: 180° C.
- Ionization method: EI+ mode
- Ionization voltage: 70 eV
- In the following Examples and Comparative Examples, the removal rate of ortho-phenyl phenol from the essential oil (each citrus oil) was obtained by the following mathematical formula (1):
-
Ortho-phenyl phenol removal rate (%)={(A 0 −A 1)/A 0}×100 (1) - wherein A0 is the content (ppm) of ortho-phenyl phenol in an essential oil (citrus oil) before purification treatment, and A1 is the content (ppm) of ortho-phenyl phenol in an essential oil (citrus oil) after purification treatment.
- (1) Five kinds of adsorbents shown in Table 1 were added to 5 g of grapefruit cold press oil in which ortho-phenyl phenol remains (ortho-phenyl phenol concentration=49.1 ppm) respectively in an amount of 1% by mass, 2% by mass, 4% by mass or 8% by mass, based on the mass of the grapefruit cold press oil, followed by well suspending and then stirring at room temperature (25° C.) for 1 hour. The adsorbent was filtered to recover the grapefruit cold press oil.
- (2) The content of ortho-phenyl phenol in the grapefruit cold press oil after the treatment with the adsorbent, recovered in (1) above was analyzed with GC/MS-MS by the method described above, and removal rate (%) of the ortho-phenyl phenol was obtained according to the mathematical formula (1) above. The results obtained are shown in Table 1.
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TABLE 1 Removal Rate (%) of Ortho-Phenyl Phenol Comparative Comparative Example 1 Example 2 Example 3 Example 1 Example 2 Kind of adsorbent POLYCLAR Kuraray Coal PLUS 7305) Seisei Shirasagi1) Shirasagi A2) GM3) Silica gel 3A4) (Polyvinyl Amount of adsorbent added (Active carbon) (Active carbon) (Active carbon) (Silica gel) pyrrolidone) 1% by mass 14 11 14 13 11 2% by mass 33 25 22 2 10 4% by mass 47 33 37 0 14 8% by mass 69 44 53 0 27 1)Manufactured by Japan EnviroChemcials, Ltd. (Zinc chloride-activated powdery active carbon) 2)Manufactured by Japan EnviroChemcials, Ltd. (Steam-activated powdery active carbon) 3)Manufactured by Kuraray Chemical Co., Ltd. (Steam-activated powdery active carbon) 4)Manufactured by Fuji Silysia Chemical Ltd. (Crushed silica gel) 5)Manufactured by ISP Japan Ltd. (Polyvinyl pyrrolidone) - (3) As shown in Table 1, in Examples 1 to 3, by treating the grapefruit cold oil in which ortho-phenyl phenol (agricultural chemical) remained therein with active carbon, the removal rate of the ortho-phenyl phenol was greatly increased as compared with Comparative Examples 1 and 2 in which the grapefruit cold press oil was treated with other adsorbent comprising silica gel or polyvinyl pyrrolidone.
- Above all, in Example 1, by using “Seisei Shirasagi” which is active carbon activated with zinc chloride, as the active carbon, the ortho-phenyl phenol was efficiently removed with higher removal rate.
- (1) Zinc chloride-activated powdery active carbon (“Seisei Shirasagi”, manufactured by Japan EnviroChemicals, Ltd.) as an adsorbent was added to 5 g of grapefruit cold press oil in which ortho-phenyl phenol remained therein (ortho-phenyl phenol concentration=49.1 ppm) in an amount of 1% by mass, 2% by mass, 4% by mass or 8% by mass, based on the mass of the grapefruit cold press oil, followed by well suspending and stirring at the respective temperatures for 1 hour as shown in Table 2. Then, the adsorbent was filtered to recover the grapefruit cold press oil.
- (2) The content of ortho-phenyl phenol in the grapefruit cold press oil after the treatment with the zinc chloride-activated powdery active carbon, recovered in (1) above was analyzed with GC/MS-MS by the method described above, and the removal rate (%) of the ortho-phenyl phenol was obtained according to the mathematical formula (1) above. The results obtained are shown in Table 2.
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TABLE 2 Removal rate (%) of Ortho-Phenyl Phenol Treatment temperature (° C.) Amount of active carbon1) added −50° C. −25° C. −5° C. 2° C. 25° C.2) 40° C. 60° C. 1% by mass 20 23 23 18 14 9 8 2% by mass —3) 40 37 37 33 23 —3) 4% by mass —3) 63 48 58 47 40 —3) 8% by mass —3) 86 77 80 69 61 —3) 1)Zinc chloride-activated powdery active carbon (“Seisei Shirasagi”, manufactured by Japan EnviroChemicals Ltd. 2)Room temperature 3)Not conducted - (3) As shown in Table 2, in removing the contaminant (residual agricultural chemicals and the like) contained in the essential oil (grapefruit cold press oil) by treating with active carbon, the contaminant (residual agricultural chemicals) can be effectively removed at a temperature in a range of from −25° C. to 40° C. Above all, it was found that when the treatment is conducted at a temperature of room temperature or lower, particularly from −25° C. to 5° C., the removal rate of ortho-phenyl phenol (agricultural chemical) is improved, and particularly, the removal rate in a temperature range of from −25° C. to 2° C. is high.
- (1) Ingredients of the grapefruit cold press oil in which ortho-phenyl phenol remained therein (oil before subjecting to the treatment with active carbon) used in Example 4 were analyzed (analysis of flavor ingredients) with GC/MS-MS by the method described above, and additionally, in Example 4 (1), components of:
- (A) purified grapefruit cold press oil obtained by the treatment of adding zinc chloride-activated powdery active carbon (Seisei Shirasagi) in an amount of 8% by mass, followed by stirring at room temperature (25° C.) for 1 hour (hereinafter referred to as “purified grapefruit oil (A)”), and
- (B) purified grapefruit cold press oil obtained by the treatment of adding zinc chloride-activated powdery active carbon (Seisei Shirasagi) in an amount of 8% by mass, followed by stirring at a temperature of −25° C. for 1 hour (hereinafter referred to as “purified grapefruit oil (B)”),
- were analyzed (analysis of flavor ingredients) with GC/MS-MS by the method described above, and the residual ratio of each main flavor ingredient contained in the purified grapefruit oils (A) and (B) was obtained. The results obtained are shown in Table 3.
- The residual ratio of each ingredient (each flavor ingredient or ortho-phenyl phenol) in Table 3 was obtained by the following mathematical formula (2).
-
Residual ratio of each ingredient (%)=(C 1 /C 0)×100 (2) - wherein C0 is the content (ppm) of each ingredient in the essential oil (grapefruit oil) before subjecting to purification treatment, and C1 is the content (ppm) of each ingredient in the essential oil (purified grapefruit oil) after conducting purification treatment.
- (2) (i) 30 g of the same grapefruit cold press oil in which ortho-phenyl phenol remained therein (oil before subjecting to purification treatment) as used in Example 4 was passed through a column (inner diameter of column: 15 mm, length of silica gel filled portion: 120 mm) filled with 15 g of silica gel (crushed silica gel “Silica Gel 3A”, manufactured by Fiji Silysia Chemical Ltd.) at 25° C., thereby obtaining purified grapefruit oil having the residual ratio of ortho-phenyl phenol of 23% (removal rate of ortho-phenyl phenol: 77%) (hereinafter referred to as “purified grapefruit oil (C)”) as shown in Table 3 below.
- (ii) The purified grapefruit oil (C) obtained in (i) above was analyzed (analysis of flavor ingredients) with GC/MS-MS by the method described above, and the residual ratio of each main flavor ingredient contained in the purified grapefruit oil (C) was obtained by the mathematical formula (2) above. The results obtained are shown in Table 3.
-
TABLE 3 Residual Ratio of Flavor Component and Ortho-Phenyl Phenol Kind of Citrus Oil Non-purified Purified Purified Purified grapefruit grapefruit grapefruit grapefruit oil1) oil2) oil3) oil4) Flavor ingredient Nootkatone 100% 100% 82% 7% Octanal 100% 100% 100% 79% Nonanal 100% 100% 100% 69% Decanal 100% 100% 100% 77% Dodecanal 100% 100% 100% 100% Linalool 100% 100% 93.5% 100% Agricultural chemical: Ortho-phenyl phenol 100% 31% 14% 23% (Removal rate: 69%) (Removal rate: 86%) (Removal rate: 77%) 1)Grapefruit cold press oil before subjecting to the treatment with active carbon 2)Purified grapefruit cold press oil obtained by adding zinc chloride-activated active carbon powder in an amount of 8% by mass, and stirring at room temperature (25° C.) for 1 hour 3)Purified grapefruit cold press oil obtained by adding zinc chloride-activated active carbon powder in an amount of 8% by mass, and stirring at −25° C. for 1 hour 4)Purified grapefruit cold press oil obtained by passing through a silica gel column at 25° C. - (3) As shown in Table 3, in the purified citrus oils (purified grapefruit oil (A) and purified grapefruit oil (B)) obtained by treating citrus oil (grapefruit cold press oil) in which agricultural chemical (ortho-phenyl phenol) remained therein with active carbon, the agricultural chemical (ortho-phenyl phenol) is smoothly removed with high removal rate. Additionally, decrease in flavor ingredients contained in the citrus oil (purified grapefruit oils (A) and (B)) is extremely small (residual ratio of flavor ingredients is extremely high), and poor balance of flavor and decrease in flavor strength did not almost occur.
- Contrary to this, in the purified citrus oil (purified grapefruit oil (C)) obtained by treating the citrus oil (grapefruit cold press oil) in which agricultural chemical (ortho-phenyl phenol) remained therein with silica gel, in the case of increasing the removal rate of the agricultural chemical (ortho-phenyl phenol) (in the case where the residual ratio of ortho-phenyl phenol was low as 23%), of the flavor ingredients contained in the citrus oil (purified grapefruit oil (C)), the residual ratio of nootkatone was extremely low, and almost all of nootkatone was lost. Additionally, octanal, nonanal and decanal were lost in considerable amounts, causing poor balance of flavor, and decrease of flavor strength.
- (4) Ten skilled panelists conducted functional evaluation on flavor strength and odor quality of grapefruit cold press oil before subjecting to the treatment with active carbon, and flavor strength and odor quality of the purified grapefruit oil (B) obtained by adding active carbon (Seisei Shirasagi) in an amount of 8% by mass and adsorption-treating at −25° C. for 1 hour under stirring. As a result, nine panelists of ten panelists judged that there is no great difference between the grapefruit oil before subjecting to the treatment with active carbon and the purified grapefruit oil (B) treated with active carbon.
- Furthermore, the same ten panelists conducted functional evaluation on flavor strength and odor quality of the purified grapefruit oil (C) obtained by purification-treating with silica gel. As a result, all the ten panelists judged that poor balance of flavor caused, flavor inherent in the grapefruit oil was lost, and flavor strength was greatly decreased.
- (1) 80 g of steam-activated powdery active carbon (“Shirasagi A”, manufactured by Japan EnviroChemicals, Ltd.) was added to 1 kg of lemon cold press oil, and suspended therein, followed by stirring at −25° C. for 30 minutes. 20 g of diatomaceous earth filter aid (“Celite 545”, manufactured by Showa Chemical Industry Co., Ltd.) was then added, and the solid contents were removed by pressure filtration, thereby obtaining 900 g of purified lemon cold press oil.
- (2) 100 g of a 60% ethanol aqueous solution was mixed with 100 g of the purified lemon oil obtained in (1) above, followed by liquid separation, and an ethanol layer was recovered. The ethanol layer recovered was used as a lemon flavor composition.
- (1) 50 g of steam-activated powdery active carbon (“Shirasagi A”, manufactured by Japan EnviroChemicals, Ltd.) was added to 1 kg of orange cold press oil, and suspended therein, followed by stirring at 5° C. for 1 hour. 30 g of diatomaceous earth filter aid (“Celite 545”, manufactured by Showa Chemical Industry Co., Ltd.) was then added, and the solid contents were removed by pressure filtration, thereby obtaining 900 g of purified orange oil.
- (2) 100 g of the purified orange oil obtained in (1) above was distilled under reduced pressure, thereby recovering 50 g of limonene.
- (3) Distillation reside after recovering the limonene in (2) above was extracted with 80 g of a 60% ethanol aqueous solution, followed by liquid separation, and an ethanol layer was recovered. The ethanol layer recovered was used as an orange flavor composition.
- (1) 300 g of ethanol and 40 g of zinc chloride-activated powdery active carbon (“Seisei Shirasagi”, manufactured by Japan EnviroChemicals, Ltd.) were added to 500 g of grapefruit oil, and the resulting mixture was stirred at 10° C. for 1 hour. 40 g of diatomaceous earth filter aid (“Celite 545”, manufactured by Showa Chemical Industry Co., Ltd.) was then added, and the solid contents were removed by pressure filtration, thereby obtaining purified grapefruit oil.
- (2) 200 g of ion-exchanged water was added to the purified grapefruit oil obtained in (1) above, and then allowed to stand. Ethanol layer was recovered, and the ethanol layer recovered was used as a grapefruit flavor composition.
- Using the orange flavor composition prepared in Example 6, fruit juice drink was prepared by using the ingredients shown in Table 4 below in amounts of the formulation shown in Table 4, uniformly mixing at 25° C., and then cooling to 5° C. The drink obtained had good orange flavor.
-
TABLE 4 Formulation (g) of Fruit Juice Drink High-fructose glucose syrup 107.0 Citric acid 1.0 Sodium citrate 0.3 Orange-concentrated juice 51.8 Water-soluble orange flavor 1.0 Orange flavor composition prepared in Example 6 0.15 Water Remainder Total 1000.0 - Using the lemon flavor composition prepared in Example 5, sports drink was prepared by using the ingredients shown in Table 5 below in amounts of the formulation shown in Table 5, uniformly mixing at 25° C., and then cooling to 5° C. The drink thus obtained had lemon flavored fresh aroma.
-
TABLE 5 Formulation (g) of Sports Drink Sugar 31.0 Glucose 15.7 Citric acid 1.0 Calcium Lactate 0.679 Sodium citrate 0.3 Sodium chloride 0.28 Potassium chloride 0.22 Vitamin C 0.864 Sodium L-glutamate 0.03 Niacin 0.013 Calcium pantothenate 0.007 Vitamin B6 0.022 Vitamin B12 0.00006 Lemon flavor 1.0 Lemon Flavor composition prepared in Example 5 0.1 Purified water Remainder Total 1000.0 - Using the lemon flavor composition prepared in Example 5, carbonated drink was prepared by using the ingredients shown in Table 6 below in amounts of the formulation shown in Table 6, uniformly mixing at 15° C. under pressure, and then cooling to 5° C. The carbonated drink thus obtained had good taste and aroma since carboxylic acid was matched up with lemon flavor.
-
TABLE 6 Formulation (g) of Carbonated Drink High-fructose glucose syrup 127.0 Citric acid 1.24 Purified water 200.0 Lemon flavor 1.0 Lemon flavor composition prepared in Example 5 0.1 Carbonated water Remainder Total 1000.0 - Using the grapefruit flavor composition prepared in Example 7, health drink was prepared by using the ingredients shown in Table 7 below in amounts of the formulation shown in Table 7, uniformly mixing at 25° C., and then cooling to 5° C. The health drink thus obtained had good grapefruit flavor.
-
TABLE 7 Formulation (g) of Health Drink White sugar 20.0 Sorbit 3.0 Citric acid 0.25 DL-malic acid 0.05 Aminoethylsulfonic acid 0.50 Glucuronolactone 0.50 Thiamine chloride 0.002 Riboflavin 0.005 Pyridoxine chloride 0.005 Caffeine 0.05 Nicotinic-acid amide 0.02 Purified honey 2.0 Grapefruit flavor 1.0 Grapefruit flavor composition prepared in Example 7 0.1 Purified water Remainder Total 1000.0 - Using the lemon flavor composition prepared in Example 5, dentifrice was prepared by using the ingredients shown in Table 8 below in amounts of the formulation shown in Table 8, uniformly mixing at 25° C., and then cooling to room temperature. The dentifrice thus obtained had lemon flavor.
-
TABLE 8 Formulation (g) of Dentifrice Dicalcium phosphate 10.0 Sodium lauryl sulfate 2.0 Sodium carboxymethyl cellulose 0.5 Saccharine sodium 0.02 Mint flavoring agent 1.0 Citrus mint flavor 5.0 Flavor composition described in Example 4 0.5 Glycerin Remainder Total 100 - Using the orange flavor composition prepared in Example 6, dental rinse was prepared by using the ingredients shown in Table 9 below in amounts of the formulation shown in Table 9, uniformly mixing at 25° C., and then cooling to 5° C. The dental rinse thus obtained had orange flavor.
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TABLE 9 Formulation (part by mass) of Dental Rinse Ethyl alcohol 10.0 Polyoxyethylene hydrogenated castor oil 2.0 Mint flavoring agent 0.5 Saccharine sodium 0.02 Citrus flavor 0.25 Orange flavor composition prepared in Example 6 0.1 Glycerin 10.0 Purified water Remainder Total 100.0 - Using the grapefruit flavor composition prepared in Example 7, candy was manufactured by using the ingredients shown in Table 10 below in amounts of the formulation shown in Table 10, melt kneading at 100° C., extruding into a rod shape having a diameter of about 1.5 cm, solidifying by cooling, and then cutting to a given length (about 2 cm). The candy thus obtained had grapefruit flavor, had good aroma and good taste.
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TABLE 10 Formulation (part by mass) of Candy Sugar powder 50 Starch syrup 33 Citric acid 1 Grapefruit flavor 0.25 Grapefruit flavor composition prepared in Example 7 0.01 Purified water Remainder Total 100 - (1) 5.0 g of sucrose acetate isobutylate (“SAM”, manufactured by Eastman Kodak Company), 1.67 g of the orange flavor composition prepared in Example 6, 3.33 g of middle-chain triglyceride (MCT OIL) (“PANACET 810”, manufactured by Ougi Chemical Co., Ltd.) and 0.2 g of an elemi resin were placed in a 200 ml beaker, and dissolved by heating, thereby obtaining a mixture comprising the orange flavor composition.
- (2) 250 g gum arabic and 648 g of water were placed in a 1 liter beaker, and dissolved by heating, followed by sterilization. Thus, a gum arabic aqueous solution was prepared.
- (3) The mixture prepared in (1) above was added to the gum arabic aqueous solution prepared in (2) above, followed by stirring at 5,000 to 12,000 rpm for 30 minutes. The resulting mixture was further treated with a high pressure homogenizer under the condition of 100 to 300 kg/cm2, thereby preparing a flavor emulsion (cloudy).
- Using the flavor emulsion (cloudy) prepared in Example 15, fruit juice drink was prepared by using the ingredients shown in Table 11 below in amounts of the formulation shown in Table 11, uniformly mixing at 25° C., and then cooling to 5° C. The drink thus obtained had orange flavor, and maintained high appearance of preference property.
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TABLE 11 Formulation (g) of Fruit Juice Drink Using Flavor Emulsion (Cloudy) High-fructose glucose syrup 107.0 Citric acid 1.0 Sodium citrate 0.3 Orange concentrated juice 51.8 Water-soluble orange flavor 1.0 Flavor emulsion (cloudy) prepared in Example 15 0.52 Water Remainder Total 1000.0 - Citrus flavor composition was prepared by using the ingredients shown in Table 12 in the formulation shown in Table 12, and uniformly mixing at 25° C.
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TABLE 12 Formulation (g) of Citrus Flavor Composition Decanol 0.25 Dodecanol 0.25 Decanal 1.40 Dodecanal 0.75 Citral 1.85 Geranyl acetate 2.00 Terpenyl acetate 2.00 Linalyl acetate 2.50 Citronellol 2.00 Orange flavor composition prepared in Example 6 1000.00 - Agricultural chemicals and other contaminants, contained in an essential oil can be removed simply with high removal rate by the present invention, without causing poor balance of flavor and decrease in flavor strength, of the essential oil. Therefore, the present invention is extremely useful as a process for producing a purified essential oil having excellent safety and high quality.
- Although the present invention has been described in detail and by reference to the specific embodiments, it is apparent to one skilled in the art that various modifications or changes can be made without departing the spirit and scope of the present invention. The present application is based on Japanese Patent Application No. 2008-288699 filed Nov. 11, 2008, the disclosure of which is incorporated herein by reference in its entity.
Claims (15)
1. A process for producing a purified essential oil, wherein an essential oil comprising a contaminant is treated with an active carbon to remove the contaminant.
2. The process for producing a purified essential oil according to claim 1 , wherein the contaminant is a residual agricultural chemical.
3. The process for producing a purified essential oil according to claim 2 , wherein the agricultural chemical is one kind or two or more kinds selected from ortho-phenyl phenol, chloroneb, simazine, carbaryl, chlorpyrifos, imazalil, thiabendazole and diphenyl.
4. The process for producing a purified essential oil according to claim 1 , wherein the essential oil is one kind or a mixture of two or more kinds selected from citrus oil, spice oil and herb oil
5. The process for producing a purified essential oil according to claim 4 , wherein the citrus oil is one kind or a mixture of two or more kinds selected from lemon oil, sweet orange oil, bitter orange oil, lime oil, grapefruit oil, bergamot oil, mandarin oil, Yuzu oil (Citrus junos oil) and Sudachi oil (Citrus sudachi oil).
6. The process for producing a purified essential oil according to claim 4 , wherein the spice oil is one kind or a mixture of two or more kinds selected from allspice, anise oil, star anise oil, bitter almond oil, blackcurrant oil, cinnamon oil, clove oil, ginger oil, mustard oil and pepper oil.
7. The process for producing a purified essential oil according to claim 4 , wherein the herb oil is one kind or a mixture of two or more kinds selected from sweet basil oil, celery oil, clary sage oil, eucalyptus oil, peppermint oil, mint oil and spearmint oil.
8. The process for producing a purified essential oil according to claim 1 , wherein the essential oil is treated with the active carbon at a temperature of from −30° C. to 5° C.
9. The process for producing a purified essential oil according to claim 1 , wherein the active carbon is an activated active carbon.
10. The process for producing a purified essential oil according to claim 9 , wherein the activated active carbon is an active carbon activated with a chemical.
11. The process for producing a purified essential oil according to claim 10 , wherein the chemical is zinc chloride.
12. A purified essential oil obtained by the production process according to claim 1 .
13. A flavor composition comprising the purified essential oil according to claim 12 .
14. A food or drink comprising the purified essential oil according to claim 12 and/or the flavor composition according to claim 13 .
15. An oral care product comprising the purified essential oil according to claim 12 and/or the flavor composition according to claim 13 .
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US (2) | US20110212037A1 (en) |
JP (1) | JP5352194B2 (en) |
TW (1) | TWI440710B (en) |
WO (1) | WO2010055864A1 (en) |
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CN111204734A (en) * | 2020-01-20 | 2020-05-29 | 上海应用技术大学 | Flaky biomass carbon material and preparation method thereof |
CN114159985A (en) * | 2021-12-30 | 2022-03-11 | 江苏久膜高科技股份有限公司 | Composite membrane for purifying lavender essential oil and preparation method thereof |
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- 2009-11-11 US US13/127,763 patent/US20110212037A1/en not_active Abandoned
- 2009-11-11 TW TW098138209A patent/TWI440710B/en not_active IP Right Cessation
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Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8791282B2 (en) | 2011-06-28 | 2014-07-29 | Givudan S.A. | Ionic liquids for agricultural residue removal |
DE102013000530A1 (en) * | 2013-01-14 | 2014-07-17 | Beiersdorf Ag | Purifying perfume oil useful for producing allergy potential-free cosmetic- and/or dermatological formulations, comprises passing the perfume oil to be cleaned through an activated carbon fixed bed |
CN111204734A (en) * | 2020-01-20 | 2020-05-29 | 上海应用技术大学 | Flaky biomass carbon material and preparation method thereof |
CN114159985A (en) * | 2021-12-30 | 2022-03-11 | 江苏久膜高科技股份有限公司 | Composite membrane for purifying lavender essential oil and preparation method thereof |
Also Published As
Publication number | Publication date |
---|---|
US20120219672A1 (en) | 2012-08-30 |
TWI440710B (en) | 2014-06-11 |
US9580668B2 (en) | 2017-02-28 |
TW201026844A (en) | 2010-07-16 |
JP5352194B2 (en) | 2013-11-27 |
JP2010116434A (en) | 2010-05-27 |
WO2010055864A1 (en) | 2010-05-20 |
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