WO2022264355A1 - 香味成型体及びその製造方法、たばこ材料の製造方法、並びにたばこ製品の製造方法 - Google Patents
香味成型体及びその製造方法、たばこ材料の製造方法、並びにたばこ製品の製造方法 Download PDFInfo
- Publication number
- WO2022264355A1 WO2022264355A1 PCT/JP2021/023020 JP2021023020W WO2022264355A1 WO 2022264355 A1 WO2022264355 A1 WO 2022264355A1 JP 2021023020 W JP2021023020 W JP 2021023020W WO 2022264355 A1 WO2022264355 A1 WO 2022264355A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- flavor
- tobacco
- alcohol
- raw material
- molding
- Prior art date
Links
- 241000208125 Nicotiana Species 0.000 title claims abstract description 132
- 235000002637 Nicotiana tabacum Nutrition 0.000 title claims abstract description 132
- 239000000796 flavoring agent Substances 0.000 title claims abstract description 122
- 235000019634 flavors Nutrition 0.000 title claims abstract description 122
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 46
- 239000000463 material Substances 0.000 title claims abstract description 34
- 235000019505 tobacco product Nutrition 0.000 title claims description 31
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 108
- 239000000843 powder Substances 0.000 claims abstract description 68
- 238000000748 compression moulding Methods 0.000 claims abstract description 21
- 239000000203 mixture Substances 0.000 claims abstract description 21
- 239000002245 particle Substances 0.000 claims abstract description 21
- 238000002156 mixing Methods 0.000 claims abstract description 14
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 8
- 239000002994 raw material Substances 0.000 claims description 68
- 238000000034 method Methods 0.000 claims description 42
- 238000000465 moulding Methods 0.000 claims description 37
- 230000006835 compression Effects 0.000 claims description 30
- 238000007906 compression Methods 0.000 claims description 30
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 claims description 24
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 18
- 239000002612 dispersion medium Substances 0.000 claims description 17
- 235000019445 benzyl alcohol Nutrition 0.000 claims description 8
- 238000003860 storage Methods 0.000 abstract description 12
- 239000011230 binding agent Substances 0.000 description 11
- 239000001913 cellulose Substances 0.000 description 11
- 235000010980 cellulose Nutrition 0.000 description 11
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- 238000011156 evaluation Methods 0.000 description 9
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- 230000000052 comparative effect Effects 0.000 description 8
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- 150000001298 alcohols Chemical class 0.000 description 6
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- 239000002002 slurry Substances 0.000 description 5
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- 229920000168 Microcrystalline cellulose Polymers 0.000 description 4
- 229920002472 Starch Polymers 0.000 description 4
- 235000019504 cigarettes Nutrition 0.000 description 4
- 150000002148 esters Chemical class 0.000 description 4
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- 235000020357 syrup Nutrition 0.000 description 4
- 239000006188 syrup Substances 0.000 description 4
- OWEGMIWEEQEYGQ-UHFFFAOYSA-N 100676-05-9 Natural products OC1C(O)C(O)C(CO)OC1OCC1C(O)C(O)C(O)C(OC2C(OC(O)C(O)C2O)CO)O1 OWEGMIWEEQEYGQ-UHFFFAOYSA-N 0.000 description 3
- GUBGYTABKSRVRQ-PICCSMPSSA-N Maltose Natural products O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1O[C@@H]1[C@@H](CO)OC(O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-PICCSMPSSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- BTANRVKWQNVYAZ-UHFFFAOYSA-N butan-2-ol Chemical compound CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- -1 for example Chemical compound 0.000 description 3
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 3
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- 238000005507 spraying Methods 0.000 description 3
- SRBFZHDQGSBBOR-IOVATXLUSA-N D-xylopyranose Chemical compound O[C@@H]1COC(O)[C@H](O)[C@H]1O SRBFZHDQGSBBOR-IOVATXLUSA-N 0.000 description 2
- 241000196324 Embryophyta Species 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- PYMYPHUHKUWMLA-UHFFFAOYSA-N arabinose Natural products OCC(O)C(O)C(O)C=O PYMYPHUHKUWMLA-UHFFFAOYSA-N 0.000 description 2
- SRBFZHDQGSBBOR-UHFFFAOYSA-N beta-D-Pyranose-Lyxose Natural products OC1COC(O)C(O)C1O SRBFZHDQGSBBOR-UHFFFAOYSA-N 0.000 description 2
- 238000005520 cutting process Methods 0.000 description 2
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- 229930195729 fatty acid Natural products 0.000 description 2
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- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 239000013081 microcrystal Substances 0.000 description 2
- 150000008163 sugars Chemical class 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- HDTRYLNUVZCQOY-UHFFFAOYSA-N α-D-glucopyranosyl-α-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OC1C(O)C(O)C(O)C(CO)O1 HDTRYLNUVZCQOY-UHFFFAOYSA-N 0.000 description 1
- SNICXCGAKADSCV-JTQLQIEISA-N (-)-Nicotine Chemical compound CN1CCC[C@H]1C1=CC=CN=C1 SNICXCGAKADSCV-JTQLQIEISA-N 0.000 description 1
- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical compound OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 1
- AFPLNGZPBSKHHQ-UHFFFAOYSA-N Betulaprenol 9 Natural products CC(C)=CCCC(C)=CCCC(C)=CCCC(C)=CCCC(C)=CCCC(C)=CCCC(C)=CCCC(C)=CCCC(C)=CCO AFPLNGZPBSKHHQ-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- WQZGKKKJIJFFOK-QTVWNMPRSA-N D-mannopyranose Chemical compound OC[C@H]1OC(O)[C@@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-QTVWNMPRSA-N 0.000 description 1
- 102000004190 Enzymes Human genes 0.000 description 1
- 108090000790 Enzymes Proteins 0.000 description 1
- 239000004386 Erythritol Substances 0.000 description 1
- UNXHWFMMPAWVPI-UHFFFAOYSA-N Erythritol Natural products OCC(O)C(O)CO UNXHWFMMPAWVPI-UHFFFAOYSA-N 0.000 description 1
- 229930091371 Fructose Natural products 0.000 description 1
- RFSUNEUAIZKAJO-ARQDHWQXSA-N Fructose Chemical compound OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@@H]1O RFSUNEUAIZKAJO-ARQDHWQXSA-N 0.000 description 1
- 239000005715 Fructose Substances 0.000 description 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 1
- YKVWPZJHENXDAJ-VOTSOKGWSA-N Megastigmatrienone Chemical compound CC1=CC(=O)CC(C)(C)C1\C=C\C=C YKVWPZJHENXDAJ-VOTSOKGWSA-N 0.000 description 1
- 241000935974 Paralichthys dentatus Species 0.000 description 1
- 238000003332 Raman imaging Methods 0.000 description 1
- HDTRYLNUVZCQOY-WSWWMNSNSA-N Trehalose Natural products O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@@H]1O[C@@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 HDTRYLNUVZCQOY-WSWWMNSNSA-N 0.000 description 1
- TVXBFESIOXBWNM-UHFFFAOYSA-N Xylitol Natural products OCCC(O)C(O)C(O)CCO TVXBFESIOXBWNM-UHFFFAOYSA-N 0.000 description 1
- HDTRYLNUVZCQOY-LIZSDCNHSA-N alpha,alpha-trehalose Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 HDTRYLNUVZCQOY-LIZSDCNHSA-N 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- PYMYPHUHKUWMLA-WDCZJNDASA-N arabinose Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)C=O PYMYPHUHKUWMLA-WDCZJNDASA-N 0.000 description 1
- 238000000149 argon plasma sintering Methods 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 235000019506 cigar Nutrition 0.000 description 1
- 230000001143 conditioned effect Effects 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- UNXHWFMMPAWVPI-ZXZARUISSA-N erythritol Chemical compound OC[C@H](O)[C@H](O)CO UNXHWFMMPAWVPI-ZXZARUISSA-N 0.000 description 1
- 235000019414 erythritol Nutrition 0.000 description 1
- 229940009714 erythritol Drugs 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 235000012907 honey Nutrition 0.000 description 1
- 238000007602 hot air drying Methods 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 239000000832 lactitol Substances 0.000 description 1
- 235000010448 lactitol Nutrition 0.000 description 1
- VQHSOMBJVWLPSR-JVCRWLNRSA-N lactitol Chemical compound OC[C@H](O)[C@@H](O)[C@@H]([C@H](O)CO)O[C@@H]1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O VQHSOMBJVWLPSR-JVCRWLNRSA-N 0.000 description 1
- 229960003451 lactitol Drugs 0.000 description 1
- 239000008101 lactose Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- VQHSOMBJVWLPSR-WUJBLJFYSA-N maltitol Chemical compound OC[C@H](O)[C@@H](O)[C@@H]([C@H](O)CO)O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O VQHSOMBJVWLPSR-WUJBLJFYSA-N 0.000 description 1
- 239000000845 maltitol Substances 0.000 description 1
- 235000010449 maltitol Nutrition 0.000 description 1
- 229940035436 maltitol Drugs 0.000 description 1
- HEBKCHPVOIAQTA-UHFFFAOYSA-N meso ribitol Natural products OCC(O)C(O)C(O)CO HEBKCHPVOIAQTA-UHFFFAOYSA-N 0.000 description 1
- 229960002715 nicotine Drugs 0.000 description 1
- SNICXCGAKADSCV-UHFFFAOYSA-N nicotine Natural products CN1CCCC1C1=CC=CN=C1 SNICXCGAKADSCV-UHFFFAOYSA-N 0.000 description 1
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- AFPLNGZPBSKHHQ-MEGGAXOGSA-N solanesol Chemical compound CC(C)=CCC\C(C)=C\CC\C(C)=C\CC\C(C)=C\CC\C(C)=C\CC\C(C)=C\CC\C(C)=C\CC\C(C)=C\CC\C(C)=C\CO AFPLNGZPBSKHHQ-MEGGAXOGSA-N 0.000 description 1
- 229940100515 sorbitan Drugs 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
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- 230000000638 stimulation Effects 0.000 description 1
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- HEBKCHPVOIAQTA-SCDXWVJYSA-N xylitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)CO HEBKCHPVOIAQTA-SCDXWVJYSA-N 0.000 description 1
- 229960002675 xylitol Drugs 0.000 description 1
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Classifications
-
- A—HUMAN NECESSITIES
- A24—TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
- A24B—MANUFACTURE OR PREPARATION OF TOBACCO FOR SMOKING OR CHEWING; TOBACCO; SNUFF
- A24B15/00—Chemical features or treatment of tobacco; Tobacco substitutes, e.g. in liquid form
- A24B15/18—Treatment of tobacco products or tobacco substitutes
- A24B15/28—Treatment of tobacco products or tobacco substitutes by chemical substances
- A24B15/30—Treatment of tobacco products or tobacco substitutes by chemical substances by organic substances
- A24B15/32—Treatment of tobacco products or tobacco substitutes by chemical substances by organic substances by acyclic compounds
-
- A—HUMAN NECESSITIES
- A24—TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
- A24B—MANUFACTURE OR PREPARATION OF TOBACCO FOR SMOKING OR CHEWING; TOBACCO; SNUFF
- A24B13/00—Tobacco for pipes, for cigars, e.g. cigar inserts, or for cigarettes; Chewing tobacco; Snuff
-
- A—HUMAN NECESSITIES
- A24—TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
- A24B—MANUFACTURE OR PREPARATION OF TOBACCO FOR SMOKING OR CHEWING; TOBACCO; SNUFF
- A24B15/00—Chemical features or treatment of tobacco; Tobacco substitutes, e.g. in liquid form
- A24B15/10—Chemical features of tobacco products or tobacco substitutes
-
- A—HUMAN NECESSITIES
- A24—TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
- A24B—MANUFACTURE OR PREPARATION OF TOBACCO FOR SMOKING OR CHEWING; TOBACCO; SNUFF
- A24B15/00—Chemical features or treatment of tobacco; Tobacco substitutes, e.g. in liquid form
- A24B15/10—Chemical features of tobacco products or tobacco substitutes
- A24B15/12—Chemical features of tobacco products or tobacco substitutes of reconstituted tobacco
- A24B15/14—Chemical features of tobacco products or tobacco substitutes of reconstituted tobacco made of tobacco and a binding agent not derived from tobacco
-
- A—HUMAN NECESSITIES
- A24—TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
- A24B—MANUFACTURE OR PREPARATION OF TOBACCO FOR SMOKING OR CHEWING; TOBACCO; SNUFF
- A24B15/00—Chemical features or treatment of tobacco; Tobacco substitutes, e.g. in liquid form
- A24B15/10—Chemical features of tobacco products or tobacco substitutes
- A24B15/16—Chemical features of tobacco products or tobacco substitutes of tobacco substitutes
-
- A—HUMAN NECESSITIES
- A24—TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
- A24B—MANUFACTURE OR PREPARATION OF TOBACCO FOR SMOKING OR CHEWING; TOBACCO; SNUFF
- A24B15/00—Chemical features or treatment of tobacco; Tobacco substitutes, e.g. in liquid form
- A24B15/18—Treatment of tobacco products or tobacco substitutes
- A24B15/28—Treatment of tobacco products or tobacco substitutes by chemical substances
-
- A—HUMAN NECESSITIES
- A24—TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
- A24B—MANUFACTURE OR PREPARATION OF TOBACCO FOR SMOKING OR CHEWING; TOBACCO; SNUFF
- A24B15/00—Chemical features or treatment of tobacco; Tobacco substitutes, e.g. in liquid form
- A24B15/18—Treatment of tobacco products or tobacco substitutes
- A24B15/28—Treatment of tobacco products or tobacco substitutes by chemical substances
- A24B15/285—Treatment of tobacco products or tobacco substitutes by chemical substances characterised by structural features, e.g. particle shape or size
-
- A—HUMAN NECESSITIES
- A24—TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
- A24B—MANUFACTURE OR PREPARATION OF TOBACCO FOR SMOKING OR CHEWING; TOBACCO; SNUFF
- A24B15/00—Chemical features or treatment of tobacco; Tobacco substitutes, e.g. in liquid form
- A24B15/18—Treatment of tobacco products or tobacco substitutes
- A24B15/28—Treatment of tobacco products or tobacco substitutes by chemical substances
- A24B15/30—Treatment of tobacco products or tobacco substitutes by chemical substances by organic substances
Definitions
- the present invention relates to a flavor molding and its manufacturing method, a tobacco material manufacturing method, and a tobacco product manufacturing method.
- Patent Literature 1 discloses a method for adding flavoring, in which leaf tobacco particles are suspended in a dispersion medium and then added to raw leaf tobacco by spraying or the like. .
- Patent Documents 2 and 3 disclose tablet oral tobacco.
- molding is generally performed using a binder.
- Patent Document 4 tobacco shreds having a cut width of 0.6 to 1 mm are aged in an air atmosphere under sealed conditions, and a polyol is added to the shredded tobacco after maturing, thereby enhancing an ester aroma component. It is also disclosed that a tobacco material can be produced in which the composition of components contributing to flavor and taste does not easily change over time.
- the binder used in the molding of oral tobacco tablets improves the moldability (strength) of tablets, but may reduce the flavor. Therefore, it is desired to develop a flavor molding having sufficient strength and good flavor.
- the present invention provides a molded flavor product that is easy to store and transport, suppresses volatilization of flavor components during storage and transport, has sufficient strength, and has a good flavor, and a tobacco material using the molded flavor product. and to provide tobacco products.
- the present invention includes the following embodiments.
- a method for producing a flavor molded body comprising:
- a method of manufacturing tobacco material comprising:
- a method of manufacturing a tobacco product comprising:
- a flavor molded article which is easy to store and transport, suppresses volatilization of flavor components during storage and transport, has sufficient strength, and has a good flavor, and a flavor molded body using the flavor molded body.
- tobacco materials and tobacco products can be provided.
- the method for producing a molded flavor product includes the following steps.
- a step of mixing a tobacco powder raw material having an average particle size of 100 ⁇ m or less with an alcohol having 2 to 7 carbon atoms to form a mixture (hereinafter also referred to as an “alcohol mixing step”); a step of compression molding the mixture (hereinafter , also referred to as a “compression molding step”); a step of removing at least part of the alcohol from the mixture (hereinafter also referred to as an “alcohol removal step”).
- a tobacco powder raw material having an average particle size of 100 ⁇ m or less is mixed with an alcohol having 2 to 7 carbon atoms and then compression-molded, so a flavor molding having sufficient strength can be obtained.
- the resin composition derived from the tobacco powder raw material migrates to the surface of the tobacco powder raw material, and is transferred to the tobacco powder raw material through the resin composition. are bound to each other, it is presumed that a flavor molding having sufficient strength can be obtained.
- the method according to the present embodiment compression molding is performed using an alcohol having 2 to 7 carbon atoms, so there is no need to use a general binder during molding, and most of the alcohol used is removed. , it is possible to obtain a flavor molding having sufficient strength and good flavor. Therefore, the molded flavor product manufactured by the method according to the present embodiment is suitable as oral tobacco.
- leaf tobacco fine powder generated when leaf tobacco is chopped in the production of tobacco products can be used.
- fine powder of leaf tobacco is generated in the process of cutting leaf tobacco.
- Most of the fine powder is transported to a restructuring plant and restructured into a sheet in the sheet making process.
- a flavor molding can be produced using the fine powder.
- the molded flavor product can be transported to a restructuring plant and used as a starting material in the papermaking sheet process. Alternatively, it can be reused by adding it to the raw material kneading process in the production of tobacco granule raw materials.
- the leaf tobacco fine powder By forming the leaf tobacco fine powder into a flavor molding in this manner, storage and transportation are facilitated, and volatilization of flavor components during storage and transportation is suppressed. Furthermore, since the method according to the present embodiment does not use a general binder at the time of molding, the flavor molded body produced by this method does not produce any flavor other than tobacco-derived flavor, and is easy to use in the recycling process. .
- the method according to the present embodiment may include steps other than the alcohol mixing step, compression molding step, and alcohol removal step. Further, the alcohol removing step may be performed during the compression molding step or after the compression molding step, as long as it is after the alcohol mixing step.
- a tobacco powder raw material having an average particle size of 100 ⁇ m or less is mixed with an alcohol having 2 to 7 carbon atoms to form a mixture.
- Tobacco powder raw materials include leaf tobacco, leaf veins, trunks, roots, flowers and the like.
- As the leaf tobacco as described above, for example, fine powder of leaf tobacco generated when cutting leaf tobacco in the production of tobacco products can be used.
- the type of leaf tobacco is not particularly limited, and may be yellow variety, burley variety, native variety, oriental leaves, fermented leaves thereof, or the like. These tobacco powder raw materials may be used alone or in combination of two or more.
- the average particle size of the tobacco powder raw material is 100 ⁇ m or less. When the average particle size is 100 ⁇ m or less, a molded flavor product having sufficient strength without being deformed over time can be obtained.
- the average particle size is preferably 5 to 80 ⁇ m, more preferably 10 to 60 ⁇ m, even more preferably 20 to 50 ⁇ m.
- the average particle size is measured using a light scattering method.
- the carbon number of the alcohol is 2 to 7, preferably 2 to 5, more preferably 2 to 3.
- the alcohol at least one alcohol selected from the group consisting of ethanol, 2-propanol and benzyl alcohol is preferable from the viewpoint of obtaining a molded flavor having higher strength, and ethanol is most preferable.
- this step it is preferable to mix 1 to 20 parts by mass of the alcohol with 100 parts by mass of the tobacco powder raw material.
- a flavor molding having higher strength can be obtained.
- Compression molding can be easily performed by mixing 20 parts by mass or less of the alcohol with 100 parts by mass of the tobacco powder raw material.
- cellulose powder or the like may be added to the tobacco powder raw material.
- the strength of the molded flavor product is further improved.
- the method of mixing the tobacco powder raw material with the alcohol is not particularly limited, but for example, it can be mixed using a general mixer such as a V-type mixer.
- compression molding process In this step, the mixture obtained in the alcohol mixing step is compression-molded.
- the compression molding machine used for compression molding is not particularly limited, for example, a rotary tableting machine or the like can be used.
- the conditions for compression molding are not particularly limited, it is desirable to mold at a compression pressure of 2 kN or more, for example. As described above, at least part of the alcohol may be removed by natural drying or the like during compression molding.
- the shape of the molded body obtained by compression molding is not particularly limited, but may be tablet-shaped, plate-shaped, cylindrical, rod-shaped, spherical, or the like.
- Alcohol removal step In this step, at least part of the alcohol is removed from the mixture.
- at least part of the alcohol may be removed from the mixture during the compression molding step, or may be removed from the compact obtained after the compression molding step.
- the alcohol at 10 to 40°C it is preferable to remove at least part of the alcohol at 10 to 40°C.
- the temperature at which at least part of the alcohol is removed is more preferably 15 to 35°C, still more preferably 20 to 30°C.
- at least part of the alcohol at 10 to 40° C. for example, at least part of the alcohol can be removed by drying at 10 to 40° C. for 30 to 120 minutes.
- At least part of the alcohol can be removed by, for example, an electric oven, hot air drying, tunnel dryer, natural drying, or the like.
- the alcohol contained in the mixture (molded body) is preferably removed, more preferably 95% by mass or more is removed, and 99% by mass or more is removed. More preferably, it is especially preferred that all alcohol is removed.
- flavor molding The flavor molded article according to the present embodiment is manufactured by the flavor molded article manufacturing method according to the embodiment.
- the flavor molded product can be easily stored and transported, the volatilization of flavor components is suppressed during storage and transport, and it has sufficient strength and good flavor.
- the compression breaking strength of the flavor molded product with a wedge-shaped plunger is preferably 10 to 200N.
- the compressive breaking strength is 10 N or more, the shape can be maintained without easily collapsing, so storage and transportation are easy. Further, when the compressive breaking strength is 200 N or less, the flavor molding can be more easily disintegrated in the dispersion medium, and the suspension of the tobacco powder raw material can be easily prepared.
- the range of compressive breaking strength is also suitable for use as oral tobacco. More preferably, the compressive breaking strength is 20 to 150N. In addition, the compressive breaking strength is a value specifically measured by a method described later.
- the shape of the flavor molded body according to the present embodiment is not particularly limited, but may be tablet-shaped, plate-shaped, cylindrical, rod-shaped, spherical, or the like.
- the flavor molded article according to the present embodiment may be a flavor molded article formed by combining a plurality of tobacco powder raw materials having an average particle size of 100 ⁇ m or less with the resin composition derived from the tobacco powder raw material interposed therebetween. can.
- the resin composition is extracted from the inside of the particles of the tobacco powder raw material, migrates to the particle surfaces, and the particles are adhered to each other by the resin contained in the resin composition, so that sufficient strength is obtained.
- the resin derived from the tobacco powder raw material functions as a binder, the flavor molding does not need to contain a general binder and has a good flavor. It can be confirmed by Raman imaging or the like that the plurality of tobacco powder raw materials are bonded to each other through the resin composition derived from the tobacco powder raw material.
- the resin composition derived from the tobacco powder raw material can contain resins such as solanesol, neophthaladiene, and megastigmatrienone.
- the resin composition may contain one kind of the resin, or may contain two or more kinds.
- the resin composition derived from the tobacco powder raw material may contain a flavor component such as nicotine contained in the tobacco powder raw material.
- the flavor molded product according to the present embodiment is a flavor molded product containing tobacco powder raw materials having an average particle size of 100 ⁇ m or less and a cellulose content of 5 to 15% by mass, wherein at least one of the cellulose It can be a flavor molding in which the part is dehydrated and condensed. It is presumed that some hydroxyl groups of cellulose contained in the tobacco powder raw material are dehydrated and condensed with nearby cellulose to obtain a flavor molding having sufficient strength.
- a preferred compression breaking strength range (10 to 200N) for the flavor molding according to the present embodiment The cellulose content of the tobacco powder raw material can be measured by the TAPPI method or the like. Moreover, it can be confirmed by NMR spectrum analysis or the like that at least part of the cellulose is dehydrated and condensed.
- the molded flavor material according to the present embodiment is produced by adding the molded flavor material to a dispersion medium, producing a tobacco material in which the tobacco powder raw material is dispersed in the dispersion medium, and converting the tobacco material into a tobacco product.
- a dispersion medium producing a tobacco material in which the tobacco powder raw material is dispersed in the dispersion medium, and converting the tobacco material into a tobacco product.
- the flavor molded product according to the present embodiment is suitable as oral tobacco.
- leaf tobacco fine powder generated when leaf tobacco is chopped in the production of tobacco products can be used.
- the manufacturing method of tobacco material according to this embodiment includes the following steps.
- a step of producing a flavor molded body by the method for producing a flavor molded body according to the present embodiment a step of adding the flavor molded body to a dispersion medium and manufacturing a tobacco material in which the tobacco powder raw material is dispersed in the dispersion medium.
- the method for producing a tobacco material according to the present embodiment it is possible to easily and efficiently produce a tobacco material used for imparting flavor to tobacco products.
- the flavor molded product according to the present embodiment is used instead of using a finely powdered tobacco raw material as the tobacco raw material, the tobacco raw material can be easily stored and transported, and volatilization of the flavor component during storage and transport is suppressed. be done. Furthermore, since the flavor molded article according to the present embodiment is easily disintegrated in a dispersion medium, a dispersion liquid of tobacco powder raw materials can be easily prepared.
- Dispersion media to which flavor moldings are added include, for example, water, monohydric alcohols, polyhydric alcohols, sugar alcohols, sugars, and polyhydric alcohol esters.
- Monohydric alcohols include monohydric fats such as methanol, ethanol, 1-propanol, 2-propanol, 1-butanol, 2-butanol, 2-methyl-1-propanol, 2,2-dimethylethanol, cyclohexanol, etc.
- monohydric alcohols having aromatic substituents such as group alcohols and benzyl alcohol; monohydric alcohols containing one or more halogen elements; and monohydric alcohols having one or more ether bonds.
- polyhydric alcohols include glycerin and propylene glycol.
- sugar alcohols include sorbitol, maltitol, xylitol, erythritol, lactitol, sorbitan, xylose, arabinose, mannose and trehalose.
- sugars include lactose, sugar, coupling sugar, glucose, enzyme starch syrup, acid-saccharified starch syrup, maltose starch syrup, maltose, isomerized sugar, fructose, reduced maltose, reduced starch syrup, and honey.
- polyhydric alcohol esters include fatty acid polyhydric alcohol esters such as fatty acid triglycerides. Among these, water or a combination of water and a substance soluble in water is preferable as the dispersion medium.
- the amount of the flavor molding to be added to the dispersion medium is not particularly limited, but may be, for example, 5 to 100 parts by mass with respect to 100 parts by mass of the dispersion medium.
- the tobacco material produced by the method according to the present embodiment can be in the form of a slurry in which the tobacco powder raw material for the flavor molded product is dispersed in a dispersion medium.
- a method for manufacturing a tobacco product according to this embodiment includes the following steps.
- the method for manufacturing a tobacco product according to the present embodiment it is possible to evenly impart flavor to the tobacco product.
- the tobacco material is manufactured by the tobacco material manufacturing method according to the present embodiment, the above-described effects based on the tobacco material manufacturing method according to the present embodiment can be obtained.
- Tobacco products to which tobacco materials are added are not particularly limited, but examples include leaf tobacco, dried leaf tobacco, flavored leaf tobacco, shredded tobacco, cigarettes, cigars, pipes, hookah, hookah, buccal tobacco, and snuff.
- the method of adding the tobacco material is not particularly limited, but spraying the tobacco material onto the tobacco product using a sprayer is preferable because the flavor components contained in the tobacco material can be more uniformly imparted to the tobacco product.
- the compressive strength at break of the compression molded product was measured and the flavor was evaluated by the following methods.
- Compression breaking strength was measured with a wedge-shaped plunger using a tablet hardness tester for the produced compression molding. Specifically, a wedge-shaped plunger (trade name: TH-1, manufactured by AS ONE Co., Ltd.) is gradually lowered against the compression molded body, and the strength when the compression molded body is compressed and broken is measured as tablet hardness. Measurement was performed three times using a meter (trade name: TH-1, manufactured by AS ONE Corporation). The average value of the values measured three times was taken as the compressive breaking strength (N).
- a slurry was prepared by adding 6 times the amount of water to the weight of the produced compression-molded body and suspending it. 2.8 g of the slurry was added to 20 g of a commercially available tobacco product (cut tobacco) by spraying to impart flavor to the tobacco product. The tobacco product was then conditioned at 22° C. and 60% relative humidity for 24 hours. Cigarettes were produced using the harmonized tobacco products, and sensory evaluations of flavor were carried out. The sensory evaluation was conducted by well-trained panelists. Further, when a cigarette was prepared in the same manner as the slurry except that the tobacco powder raw material was used as it was instead of the compacted body, and sensory evaluation was performed (Reference), the sugar odor and orange taste increased.
- Example 1 3 parts by mass of ethanol was added to 100 parts by mass of a tobacco powder raw material consisting of leaf tobacco (Brazilian fluke) having an average particle size of 30 ⁇ m and mixed. The resulting mixture was molded into tablets using a compression molding machine (trade name: TDP 0, manufactured by LFA Machines Oxford Ltd.). The obtained molded body was dried at 20° C. for 2 days to remove the ethanol contained in the molded body to obtain a compression molded body. The compressive breaking strength of the compression-molded body was measured by the method described above. Table 1 shows the results.
- Example 2 to 4 A compression molded body was produced in the same manner as in Example 1, except that the amount of ethanol added was changed as shown in Table 1, and the compression breaking strength was measured. Moreover, the flavor evaluation of the flavor molding of Example 3 was performed by the method described above. Table 1 shows the results.
- Example 5 A compression molded body was produced in the same manner as in Example 3 except that the molded body after molding with a compression molding machine was dried at 40° C. for 2 hours to remove ethanol contained in the molded body, and the compression breaking strength was measured. Moreover, the flavor evaluation was performed by the said method. Table 1 shows the results.
- Example 1 A compression molded body was produced in the same manner as in Example 1, except that ethanol was not mixed with the tobacco powder raw material, and the compression breaking strength was measured. Table 1 shows the results.
- Example 2 Example 1, except that 40 parts by mass of microcrystalline cellulose (trade name: cellulose, microcrystal, manufactured by Alfa aesar) as a binder was added instead of ethanol to 100 parts by mass of the tobacco powder raw material and mixed. A compression-molded body was produced in the same manner, and the compression breaking strength was measured. Table 1 shows the results.
- microcrystalline cellulose trade name: cellulose, microcrystal, manufactured by Alfa aesar
- Example 4 A compression-molded body was produced and compressed in the same manner as in Example 3, except that a tobacco powder raw material consisting of leaf tobacco having an average particle size of 0.68 mm (particle size: 0.35 to 1.0 mm) was used as the tobacco powder raw material. Breaking strength was measured. However, after molding, the molded body expanded with time, and the shape of the molded body could not be maintained, so the compressive breaking strength could not be measured.
- Comparative Example 1 in which ethanol was not added, had a lower compressive breaking strength than the examples in which ethanol was added.
- Comparative Example 2 in which 40 parts by mass of microcrystalline cellulose was added as a binder, had a lower compressive breaking strength than the Examples in which ethanol was added.
- Comparative Example 3 in which 80 parts by mass of microcrystalline cellulose was added as a binder, the compression breaking strength was high, but the stimulation and fiber odor derived from the binder were conspicuous in the flavor evaluation, and the flavor was inferior to that of Examples. was bad.
- Comparative Example 4 in which the tobacco powder raw material had an average particle size of more than 100 ⁇ m, the shape of the molded product could not be maintained after molding, and the compression molded product was unsatisfactory.
- Example 6 A compression molded body was produced in the same manner as in Example 1, except that 5 parts by mass of benzyl alcohol was added instead of ethanol to 100 parts by mass of the tobacco powder raw material, and the compression breaking strength was measured. Table 2 shows the results.
- Example 7 A compression molded body was produced in the same manner as in Example 6, except that the amount of benzyl alcohol added was changed as shown in Table 2, and the compression breaking strength was measured. Table 2 shows the results.
- Example 9 A compression molded body was produced in the same manner as in Example 1, except that 3 parts by mass of 2-propanol was added instead of ethanol to 100 parts by mass of the tobacco powder raw material, and the compression breaking strength was measured. Table 2 shows the results.
- Example 10-12 A compression molded body was produced in the same manner as in Example 9, except that the amount of benzyl alcohol added was changed as shown in Table 2, and the compression breaking strength was measured. Table 2 shows the results.
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Abstract
Description
前記混合物を圧縮成型する工程と、
前記混合物から前記アルコールの少なくとも一部を除去する工程と、
を含む、香味成型体の製造方法。
前記香味成型体を分散媒体に添加し、該分散媒体中に前記たばこ粉末原料が分散したたばこ材料を製造する工程と、
を含む、たばこ材料の製造方法。
前記たばこ材料をたばこ製品に添加する工程と、
を含む、たばこ製品の製造方法。
本実施形態に係る香味成型体の製造方法は、以下の工程を含む。平均粒子径が100μm以下のたばこ粉末原料に、炭素数2~7のアルコールを混合して混合物を形成する工程(以下、「アルコール混合工程」ともいう。);前記混合物を圧縮成型する工程(以下、「圧縮成型工程」ともいう。);前記混合物から前記アルコールの少なくとも一部を除去する工程(以下、「アルコール除去工程」ともいう。)。
本工程では、平均粒子径が100μm以下のたばこ粉末原料に、炭素数2~7のアルコールを混合して混合物を形成する。たばこ粉末原料としては、葉たばこ、葉脈部、幹部、根、花等が挙げられる。前記葉たばことしては、前述したように、例えばたばこ製品の製造において葉たばこを裁刻する際に発生する葉たばこの細粉を用いることができる。前記葉たばこの種類は特に限定されず、黄色種、バーレー種、在来種、オリエント葉等や、それらの発酵葉等であることができる。これらのたばこ粉末原料は一種を用いてもよく、二種以上を併用してもよい。
本工程では、前記アルコール混合工程で得られた混合物を圧縮成型する。圧縮成型に用いられる圧縮成型機は特に限定されないが、例えば回転式打錠機等を用いることができる。圧縮成型の条件は特に限定されないが、例えば2kN以上の圧縮圧力で成形することが望ましい。なお、前述したように、例えば圧縮成型中に前記アルコールの少なくとも一部が自然乾燥等により除去されてもよい。
本工程では、前記混合物から前記アルコールの少なくとも一部を除去する。ここで、前述したように、前記アルコールの少なくとも一部の除去は、前記圧縮成型工程中に前記混合物に対して行われてもよく、前記圧縮成型工程後に得られた成型体に対して行われてもよい。
本実施形態に係る香味成型体は、本実施形態に係る香味成型体の製造方法により製造される。該香味成型体は保存や輸送が容易であり、保存や輸送中の香味成分の揮発が抑制され、十分な強度を有し、かつ香味が良好である。
本実施形態に係るたばこ材料の製造方法は、以下の工程を含む。本実施形態に係る香味成型体の製造方法により、香味成型体を製造する工程;前記香味成型体を分散媒体に添加し、該分散媒体中に前記たばこ粉末原料が分散したたばこ材料を製造する工程。本実施形態に係るたばこ材料の製造方法によれば、たばこ製品に対して香味を付与する際に用いられるたばこ材料を簡便かつ効率よく製造することができる。特に、たばこ原料として微粉末状のたばこ原料を用いる代わりに本実施形態に係る香味成型体を使用するため、たばこ原料の保存や輸送が容易であり、保存や輸送中の香味成分の揮発が抑制される。さらに、本実施形態に係る香味成型体は分散媒体中で容易に崩壊するため、簡便にたばこ粉末原料の分散液を調製することができる。
本実施形態に係るたばこ製品の製造方法は、以下の工程を含む。本実施形態に係るたばこ材料の製造方法によりたばこ材料を製造する工程;前記たばこ材料をたばこ製品に添加する工程。本実施形態に係るたばこ製品の製造方法によれば、たばこ製品に対して香味をムラなく付与することができる。特に、本実施形態に係るたばこ材料の製造方法によりたばこ材料を製造するため、前述した本実施形態に係るたばこ材料の製造方法に基づく効果が得られる。
作製した圧縮成型体に対して錠剤硬度計を用いてクサビ型プランジャにより圧縮破断強度の測定を行った。具体的には、圧縮成型体に対してクサビ型プランジャ(商品名:TH-1、アズワン株式会社製)を徐々に下していき、圧縮成型体を圧縮して破断した際の強度を錠剤硬度計(商品名:TH-1、アズワン株式会社製)を用いて3回測定した。3回測定した値の平均値を圧縮破断強度(N)とした。
作製した圧縮成型体の質量に対して6倍量の水を加えて懸濁したスラリーを調製した。該スラリー2.8gを、市販のたばこ製品(刻みたばこ)20gにスプレーにより添加し、たばこ製品に香味を付与した。その後、該たばこ製品を22℃、相対湿度60%の条件で24時間調和した。調和後のたばこ製品を用いてシガレットを作製し、香味に関する官能評価を実施した。なお、官能評価は十分に訓練がなされたパネラーにより実施した。また、圧縮成型体の代わりにたばこ粉末原料をそのまま用いてスラリーを調製した以外同様にシガレットを作製し、官能評価を実施した場合(Reference)、糖臭味、オレンジ感が増した。
平均粒子径が30μmの葉たばこ(ブラジル産黄色種)からなるたばこ粉末原料100質量部に対して、3質量部のエタノールを加えて混合した。得られた混合物を圧縮成型機(商品名:TDP 0、LFA Machines Oxford Ltd製)により錠剤形状に成型した。得られた成型体を20℃で2日間乾燥し、成型体に含まれるエタノールを除去することで、圧縮成型体を得た。該圧縮成型体について、前記方法により圧縮破断強度を測定した。結果を表1に示す。
エタノールの添加量を表1に示すように変更した以外は、実施例1と同様に圧縮成型体を作製し、圧縮破断強度を測定した。また、実施例3の香味成型体について、前記方法により香味評価を行った。結果を表1に示す。
圧縮成型機で成型後の成型体を40℃で2時間乾燥し、成型体に含まれるエタノールを除去した以外は、実施例3と同様に圧縮成型体を作製し、圧縮破断強度を測定した。また、前記方法により香味評価を行った。結果を表1に示す。
前記たばこ粉末原料にエタノールを混合しなかったこと以外は、実施例1と同様に圧縮成型体を作製し、圧縮破断強度を測定した。結果を表1に示す。
前記たばこ粉末原料100質量部に対して、エタノールの代わりに結合剤である微結晶セルロース(商品名:セルロース,微結晶、Alfa aesar製)40質量部を加えて混合した以外は、実施例1と同様に圧縮成型体を作製し、圧縮破断強度を測定した。結果を表1に示す。
前記たばこ粉末原料100質量部に対して、エタノールの代わりに結合剤である微結晶セルロース(商品名:セルロース,微結晶、Alfa aesar製)80質量部を加えて混合した以外は、実施例1と同様に圧縮成型体を作製し、圧縮破断強度を測定した。また、前記方法により香味評価を行った。結果を表1に示す。
たばこ粉末原料として、平均粒子径0.68mm(粒子径:0.35~1.0mm)の葉たばこからなるたばこ粉末原料を用いた以外は、実施例3と同様に圧縮成型体を作製し、圧縮破断強度を測定した。しかし、成型後、経時と共に成型体が膨張し、成型体の形状を維持できなかったため、圧縮破断強度の測定を実施することができなかった。
前記たばこ粉末原料100質量部に対して、エタノールの代わりにベンジルアルコールを5質量部添加した以外は、実施例1と同様に圧縮成型体を作製し、圧縮破断強度を測定した。結果を表2に示す。
ベンジルアルコールの添加量を表2に示すように変更した以外は、実施例6と同様に圧縮成型体を作製し、圧縮破断強度を測定した。結果を表2に示す。
前記たばこ粉末原料100質量部に対して、エタノールの代わりに2-プロパノールを3質量部添加した以外は、実施例1と同様に圧縮成型体を作製し、圧縮破断強度を測定した。結果を表2に示す。
ベンジルアルコールの添加量を表2に示すように変更した以外は、実施例9と同様に圧縮成型体を作製し、圧縮破断強度を測定した。結果を表2に示す。
Claims (10)
- 平均粒子径が100μm以下のたばこ粉末原料に、炭素数2~7のアルコールを混合して混合物を形成する工程と、
前記混合物を圧縮成型する工程と、
前記混合物から前記アルコールの少なくとも一部を除去する工程と、
を含む、香味成型体の製造方法。 - 前記アルコールが、エタノール、2-プロパノール及びベンジルアルコールからなる群から選択される少なくとも一種のアルコールである、請求項1に記載の香味成型体の製造方法。
- 前記混合物を形成する工程において、前記たばこ粉末原料100質量部に対して前記アルコールを1~20質量部混合する、請求項1又は2に記載の香味成型体の製造方法。
- 前記アルコールの少なくとも一部を除去する工程において、10~40℃で前記アルコールの少なくとも一部を除去する、請求項1~3のいずれか一項に記載の香味成型体の製造方法。
- 錠剤硬度計を用いて測定される、前記香味成型体のくさび型プランジャによる圧縮破断強度が10~200Nである、請求項1~4のいずれか一項に記載の香味成型体の製造方法。
- 前記たばこ粉末原料が、たばこ製品の製造において葉たばこを裁刻する際に発生する葉たばこの細粉である、請求項1~5のいずれか一項に記載の香味成型体の製造方法。
- 前記香味成型体が口腔たばこである、請求項1~6のいずれか一項に記載の香味成型体の製造方法。
- 請求項1~6のいずれか一項に記載の方法により、香味成型体を製造する工程と、
前記香味成型体を分散媒体に添加し、該分散媒体中に前記たばこ粉末原料が分散したたばこ材料を製造する工程と、
を含む、たばこ材料の製造方法。 - 請求項8に記載の方法によりたばこ材料を製造する工程と、
前記たばこ材料をたばこ製品に添加する工程と、
を含む、たばこ製品の製造方法。 - 請求項1~7のいずれか一項に記載の方法により製造される香味成型体。
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KR1020237041217A KR20240004756A (ko) | 2021-06-17 | 2021-06-17 | 향미 성형체 및 그 제조 방법, 담배 재료의 제조 방법, 및 담배 제품의 제조 방법 |
JP2023528875A JPWO2022264355A1 (ja) | 2021-06-17 | 2021-06-17 | |
EP21946032.6A EP4356760A1 (en) | 2021-06-17 | 2021-06-17 | Flavor molded article and production method therefor, tobacco material production method, and tobacco product production method |
CN202180098843.8A CN117396081A (zh) | 2021-06-17 | 2021-06-17 | 香味成型体及其制造方法、烟草材料的制造方法、以及烟草制品的制造方法 |
US18/521,520 US20240090563A1 (en) | 2021-06-17 | 2023-11-28 | Flavor molded article and production method therefor, tobacco material production method, and tobacco product production method |
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Citations (5)
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JP2011504733A (ja) * | 2007-11-28 | 2011-02-17 | フィリップ モリス ユーエスエイ インコーポレイテッド | 経口摂取のための無煙圧縮タバコ製品 |
JP2012085643A (ja) | 2003-11-07 | 2012-05-10 | Us Smokeless Tobacco Co Llc | タバコ組成物 |
WO2013098920A1 (ja) | 2011-12-26 | 2013-07-04 | 日本たばこ産業株式会社 | 増強されたエステル香気成分及び香喫味に寄与する成分を含むたばこ材料の製造方法および該方法により製造されたたばこ材料を含むたばこ製品 |
JP2013544521A (ja) * | 2010-12-01 | 2013-12-19 | アール・ジエイ・レイノルズ・タバコ・カンパニー | 無煙タバコ香錠剤及び無煙タバコ製品を形成するための射出成形プロセス |
WO2014185103A1 (ja) | 2013-05-13 | 2014-11-20 | 日本たばこ産業株式会社 | たばこ材料、該たばこ材料が添加されたたばこ製品及びたばこ材料の製造方法 |
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US20120189889A1 (en) | 2011-01-24 | 2012-07-26 | Dukjung Kim | Secondary battery |
JP2013098920A (ja) | 2011-11-04 | 2013-05-20 | Sony Corp | 欠陥補正装置、欠陥補正方法および撮像装置 |
JP2014185103A (ja) | 2013-03-22 | 2014-10-02 | L'oreal Sa | 縮合剤を用いる毛髪の持続的着色 |
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2021
- 2021-06-17 JP JP2023528875A patent/JPWO2022264355A1/ja active Pending
- 2021-06-17 KR KR1020237041217A patent/KR20240004756A/ko unknown
- 2021-06-17 EP EP21946032.6A patent/EP4356760A1/en active Pending
- 2021-06-17 CN CN202180098843.8A patent/CN117396081A/zh active Pending
- 2021-06-17 WO PCT/JP2021/023020 patent/WO2022264355A1/ja active Application Filing
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JP2012085643A (ja) | 2003-11-07 | 2012-05-10 | Us Smokeless Tobacco Co Llc | タバコ組成物 |
JP2011504733A (ja) * | 2007-11-28 | 2011-02-17 | フィリップ モリス ユーエスエイ インコーポレイテッド | 経口摂取のための無煙圧縮タバコ製品 |
JP2013544521A (ja) * | 2010-12-01 | 2013-12-19 | アール・ジエイ・レイノルズ・タバコ・カンパニー | 無煙タバコ香錠剤及び無煙タバコ製品を形成するための射出成形プロセス |
JP2017079764A (ja) | 2010-12-01 | 2017-05-18 | アール・ジエイ・レイノルズ・タバコ・カンパニー | 無煙タバコ香錠剤及び無煙タバコ製品を形成するための射出成形プロセス |
WO2013098920A1 (ja) | 2011-12-26 | 2013-07-04 | 日本たばこ産業株式会社 | 増強されたエステル香気成分及び香喫味に寄与する成分を含むたばこ材料の製造方法および該方法により製造されたたばこ材料を含むたばこ製品 |
WO2014185103A1 (ja) | 2013-05-13 | 2014-11-20 | 日本たばこ産業株式会社 | たばこ材料、該たばこ材料が添加されたたばこ製品及びたばこ材料の製造方法 |
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US20240090563A1 (en) | 2024-03-21 |
CN117396081A (zh) | 2024-01-12 |
JPWO2022264355A1 (ja) | 2022-12-22 |
KR20240004756A (ko) | 2024-01-11 |
EP4356760A1 (en) | 2024-04-24 |
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