CN101731748B - 神农香菊叶的提取方法及其提取物在卷烟中的应用 - Google Patents
神农香菊叶的提取方法及其提取物在卷烟中的应用 Download PDFInfo
- Publication number
- CN101731748B CN101731748B CN2008101975376A CN200810197537A CN101731748B CN 101731748 B CN101731748 B CN 101731748B CN 2008101975376 A CN2008101975376 A CN 2008101975376A CN 200810197537 A CN200810197537 A CN 200810197537A CN 101731748 B CN101731748 B CN 101731748B
- Authority
- CN
- China
- Prior art keywords
- dendranthema
- leaves
- indium
- extract
- extracting
- 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.)
- Active
Links
- 241000723353 Chrysanthemum Species 0.000 title claims abstract description 46
- 235000007516 Chrysanthemum Nutrition 0.000 title claims abstract description 46
- 229910052738 indium Inorganic materials 0.000 title claims abstract description 44
- APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 title claims abstract description 44
- 235000019504 cigarettes Nutrition 0.000 title claims abstract description 30
- 238000000034 method Methods 0.000 title claims abstract description 19
- 239000000284 extract Substances 0.000 claims abstract description 76
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 55
- 238000000605 extraction Methods 0.000 claims abstract description 18
- 239000000463 material Substances 0.000 claims abstract description 17
- 239000000341 volatile oil Substances 0.000 claims abstract description 16
- 239000002304 perfume Substances 0.000 claims abstract description 15
- 238000001035 drying Methods 0.000 claims abstract description 13
- 238000010992 reflux Methods 0.000 claims abstract description 9
- 238000001914 filtration Methods 0.000 claims abstract description 4
- 239000007788 liquid Substances 0.000 claims abstract description 4
- 239000000706 filtrate Substances 0.000 claims abstract description 3
- 240000005250 Chrysanthemum indicum Species 0.000 claims description 23
- 235000018959 Chrysanthemum indicum Nutrition 0.000 claims description 22
- 239000000243 solution Substances 0.000 claims description 16
- 108090000790 Enzymes Proteins 0.000 claims description 14
- 102000004190 Enzymes Human genes 0.000 claims description 14
- 229940088598 enzyme Drugs 0.000 claims description 14
- 235000012054 meals Nutrition 0.000 claims description 14
- 108010059892 Cellulase Proteins 0.000 claims description 11
- 229940106157 cellulase Drugs 0.000 claims description 11
- 239000002904 solvent Substances 0.000 claims description 11
- 241000208125 Nicotiana Species 0.000 claims description 7
- 235000002637 Nicotiana tabacum Nutrition 0.000 claims description 7
- 230000006837 decompression Effects 0.000 claims description 7
- 239000004519 grease Substances 0.000 claims description 7
- 239000008055 phosphate buffer solution Substances 0.000 claims description 7
- 238000002360 preparation method Methods 0.000 claims description 7
- 238000004064 recycling Methods 0.000 claims description 7
- 238000001256 steam distillation Methods 0.000 claims description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 7
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 238000005520 cutting process Methods 0.000 claims description 2
- 239000000945 filler Substances 0.000 claims description 2
- 238000010438 heat treatment Methods 0.000 claims description 2
- 239000002994 raw material Substances 0.000 claims description 2
- 230000000694 effects Effects 0.000 abstract description 14
- 239000000796 flavoring agent Substances 0.000 abstract description 7
- 235000019634 flavors Nutrition 0.000 abstract description 6
- 238000001704 evaporation Methods 0.000 abstract description 2
- 239000000843 powder Substances 0.000 abstract 2
- GAMYVSCDDLXAQW-AOIWZFSPSA-N Thermopsosid Natural products O(C)c1c(O)ccc(C=2Oc3c(c(O)cc(O[C@H]4[C@H](O)[C@@H](O)[C@H](O)[C@H](CO)O4)c3)C(=O)C=2)c1 GAMYVSCDDLXAQW-AOIWZFSPSA-N 0.000 description 11
- 229930003944 flavone Natural products 0.000 description 11
- 235000011949 flavones Nutrition 0.000 description 11
- VHBFFQKBGNRLFZ-UHFFFAOYSA-N vitamin p Natural products O1C2=CC=CC=C2C(=O)C=C1C1=CC=CC=C1 VHBFFQKBGNRLFZ-UHFFFAOYSA-N 0.000 description 11
- 150000002212 flavone derivatives Chemical class 0.000 description 10
- 239000000203 mixture Substances 0.000 description 9
- 239000003205 fragrance Substances 0.000 description 8
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 6
- 239000002131 composite material Substances 0.000 description 6
- 239000003546 flue gas Substances 0.000 description 6
- CDOSHBSSFJOMGT-UHFFFAOYSA-N linalool Chemical compound CC(C)=CCCC(C)(O)C=C CDOSHBSSFJOMGT-UHFFFAOYSA-N 0.000 description 6
- 238000004458 analytical method Methods 0.000 description 5
- HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 description 4
- GHVNFZFCNZKVNT-UHFFFAOYSA-N decanoic acid Chemical compound CCCCCCCCCC(O)=O GHVNFZFCNZKVNT-UHFFFAOYSA-N 0.000 description 4
- RRAFCDWBNXTKKO-UHFFFAOYSA-N eugenol Chemical compound COC1=CC(CC=C)=CC=C1O RRAFCDWBNXTKKO-UHFFFAOYSA-N 0.000 description 4
- DCAYPVUWAIABOU-UHFFFAOYSA-N hexadecane Chemical compound CCCCCCCCCCCCCCCC DCAYPVUWAIABOU-UHFFFAOYSA-N 0.000 description 4
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 4
- LQERIDTXQFOHKA-UHFFFAOYSA-N nonadecane Chemical compound CCCCCCCCCCCCCCCCCCC LQERIDTXQFOHKA-UHFFFAOYSA-N 0.000 description 4
- 230000000391 smoking effect Effects 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- OGLDWXZKYODSOB-UHFFFAOYSA-N α-phellandrene Chemical compound CC(C)C1CC=C(C)C=C1 OGLDWXZKYODSOB-UHFFFAOYSA-N 0.000 description 4
- WEEGYLXZBRQIMU-UHFFFAOYSA-N Eucalyptol Chemical compound C1CC2CCC1(C)OC2(C)C WEEGYLXZBRQIMU-UHFFFAOYSA-N 0.000 description 3
- 238000003556 assay Methods 0.000 description 3
- 229960005233 cineole Drugs 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 3
- 238000001819 mass spectrum Methods 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- BRHDDEIRQPDPMG-UHFFFAOYSA-N trans-furanoid linalool oxide Natural products CC(C)(O)C1CCC(C)(C=C)O1 BRHDDEIRQPDPMG-UHFFFAOYSA-N 0.000 description 3
- 238000010792 warming Methods 0.000 description 3
- LGNSZMLHOYDATP-UHFFFAOYSA-N (+)-4-Carene Chemical compound C1=CC(C)CC2C(C)(C)C12 LGNSZMLHOYDATP-UHFFFAOYSA-N 0.000 description 2
- LFJQCDVYDGGFCH-JTQLQIEISA-N (+)-β-phellandrene Chemical compound CC(C)[C@@H]1CCC(=C)C=C1 LFJQCDVYDGGFCH-JTQLQIEISA-N 0.000 description 2
- LFJQCDVYDGGFCH-SNVBAGLBSA-N (+/-)-beta-Phellandrene Natural products CC(C)[C@H]1CCC(=C)C=C1 LFJQCDVYDGGFCH-SNVBAGLBSA-N 0.000 description 2
- WXQGPFZDVCRBME-QEJZJMRPSA-N (-)-thujopsene Chemical compound C([C@@]1(C)CC=C2C)CCC(C)(C)[C@]11[C@H]2C1 WXQGPFZDVCRBME-QEJZJMRPSA-N 0.000 description 2
- JZQKTMZYLHNFPL-BLHCBFLLSA-N (2E,4E)-deca-2,4-dienal Chemical compound CCCCC\C=C\C=C\C=O JZQKTMZYLHNFPL-BLHCBFLLSA-N 0.000 description 2
- 239000001490 (3R)-3,7-dimethylocta-1,6-dien-3-ol Substances 0.000 description 2
- JSNRRGGBADWTMC-UHFFFAOYSA-N (6E)-7,11-dimethyl-3-methylene-1,6,10-dodecatriene Chemical compound CC(C)=CCCC(C)=CCCC(=C)C=C JSNRRGGBADWTMC-UHFFFAOYSA-N 0.000 description 2
- DCSCXTJOXBUFGB-JGVFFNPUSA-N (R)-(+)-Verbenone Natural products CC1=CC(=O)[C@@H]2C(C)(C)[C@H]1C2 DCSCXTJOXBUFGB-JGVFFNPUSA-N 0.000 description 2
- DCSCXTJOXBUFGB-SFYZADRCSA-N (R)-(+)-verbenone Chemical compound CC1=CC(=O)[C@H]2C(C)(C)[C@@H]1C2 DCSCXTJOXBUFGB-SFYZADRCSA-N 0.000 description 2
- CDOSHBSSFJOMGT-JTQLQIEISA-N (R)-linalool Natural products CC(C)=CCC[C@@](C)(O)C=C CDOSHBSSFJOMGT-JTQLQIEISA-N 0.000 description 2
- WUOACPNHFRMFPN-SECBINFHSA-N (S)-(-)-alpha-terpineol Chemical compound CC1=CC[C@@H](C(C)(C)O)CC1 WUOACPNHFRMFPN-SECBINFHSA-N 0.000 description 2
- HEVGGTGPGPKZHF-UHFFFAOYSA-N 1-(1,2-dimethyl-3-methylidenecyclopentyl)-4-methylbenzene Chemical compound CC1C(=C)CCC1(C)C1=CC=C(C)C=C1 HEVGGTGPGPKZHF-UHFFFAOYSA-N 0.000 description 2
- 239000001278 2-(5-ethenyl-5-methyloxolan-2-yl)propan-2-ol Substances 0.000 description 2
- JZQKTMZYLHNFPL-UHFFFAOYSA-N 2-trans-4-trans-decadienal Natural products CCCCCC=CC=CC=O JZQKTMZYLHNFPL-UHFFFAOYSA-N 0.000 description 2
- HOBBEYSRFFJETF-UHFFFAOYSA-N 4-Acetyl-1-methylcyclohexene Chemical compound CC(=O)C1CCC(C)=CC1 HOBBEYSRFFJETF-UHFFFAOYSA-N 0.000 description 2
- IJALWSVNUBBQRA-UHFFFAOYSA-N 4-Isopropyl-3-methylphenol Chemical compound CC(C)C1=CC=C(O)C=C1C IJALWSVNUBBQRA-UHFFFAOYSA-N 0.000 description 2
- NPBVQXIMTZKSBA-UHFFFAOYSA-N Chavibetol Natural products COC1=CC=C(CC=C)C=C1O NPBVQXIMTZKSBA-UHFFFAOYSA-N 0.000 description 2
- 239000005770 Eugenol Substances 0.000 description 2
- UVMRYBDEERADNV-UHFFFAOYSA-N Pseudoeugenol Natural products COC1=CC(C(C)=C)=CC=C1O UVMRYBDEERADNV-UHFFFAOYSA-N 0.000 description 2
- OVKDFILSBMEKLT-UHFFFAOYSA-N alpha-Terpineol Natural products CC(=C)C1(O)CCC(C)=CC1 OVKDFILSBMEKLT-UHFFFAOYSA-N 0.000 description 2
- HICYDYJTCDBHMZ-UHFFFAOYSA-N alpha-longipinene Chemical compound C12C3C(C)=CCC1C3(C)CCCC2(C)C HICYDYJTCDBHMZ-UHFFFAOYSA-N 0.000 description 2
- OGLDWXZKYODSOB-SNVBAGLBSA-N alpha-phellandrene Natural products CC(C)[C@H]1CC=C(C)C=C1 OGLDWXZKYODSOB-SNVBAGLBSA-N 0.000 description 2
- 229940088601 alpha-terpineol Drugs 0.000 description 2
- HAVYZKHVTLAPDZ-RCHZWEEESA-N beta-Humulene Natural products C\C1=C\CC(C)(C)\C=C\CC(=C)CCC1 HAVYZKHVTLAPDZ-RCHZWEEESA-N 0.000 description 2
- PHWISBHSBNDZDX-UHFFFAOYSA-N beta-Sesquiphellandrene Natural products CC(C)=CCCC(C)C1CCC(=C)C=C1 PHWISBHSBNDZDX-UHFFFAOYSA-N 0.000 description 2
- UAHWPYUMFXYFJY-UHFFFAOYSA-N beta-myrcene Chemical compound CC(C)=CCCC(=C)C=C UAHWPYUMFXYFJY-UHFFFAOYSA-N 0.000 description 2
- LFJQCDVYDGGFCH-UHFFFAOYSA-N beta-phellandrene Natural products CC(C)C1CCC(=C)C=C1 LFJQCDVYDGGFCH-UHFFFAOYSA-N 0.000 description 2
- PHWISBHSBNDZDX-LSDHHAIUSA-N beta-sesquiphellandrene Chemical compound CC(C)=CCC[C@H](C)[C@H]1CCC(=C)C=C1 PHWISBHSBNDZDX-LSDHHAIUSA-N 0.000 description 2
- 239000012159 carrier gas Substances 0.000 description 2
- RFFOTVCVTJUTAD-UHFFFAOYSA-N cineole Natural products C1CC2(C)CCC1(C(C)C)O2 RFFOTVCVTJUTAD-UHFFFAOYSA-N 0.000 description 2
- CCRCUPLGCSFEDV-UHFFFAOYSA-N cinnamic acid methyl ester Natural products COC(=O)C=CC1=CC=CC=C1 CCRCUPLGCSFEDV-UHFFFAOYSA-N 0.000 description 2
- 229960002217 eugenol Drugs 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 150000002500 ions Chemical class 0.000 description 2
- RGFNRWTWDWVHDD-UHFFFAOYSA-N isobutyl butyrate Chemical compound CCCC(=O)OCC(C)C RGFNRWTWDWVHDD-UHFFFAOYSA-N 0.000 description 2
- 229930007744 linalool Natural products 0.000 description 2
- CCRCUPLGCSFEDV-BQYQJAHWSA-N methyl trans-cinnamate Chemical compound COC(=O)\C=C\C1=CC=CC=C1 CCRCUPLGCSFEDV-BQYQJAHWSA-N 0.000 description 2
- VSMOENVRRABVKN-UHFFFAOYSA-N oct-1-en-3-ol Chemical compound CCCCCC(O)C=C VSMOENVRRABVKN-UHFFFAOYSA-N 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 description 2
- 230000001953 sensory effect Effects 0.000 description 2
- WXQGPFZDVCRBME-UHFFFAOYSA-N thujopsene Natural products CC1=CCC2(C)CCCC(C)(C)C22C1C2 WXQGPFZDVCRBME-UHFFFAOYSA-N 0.000 description 2
- DCSCXTJOXBUFGB-UHFFFAOYSA-N verbenone Natural products CC1=CC(=O)C2C(C)(C)C1C2 DCSCXTJOXBUFGB-UHFFFAOYSA-N 0.000 description 2
- NPNUFJAVOOONJE-ZIAGYGMSSA-N β-(E)-Caryophyllene Chemical compound C1CC(C)=CCCC(=C)[C@H]2CC(C)(C)[C@@H]21 NPNUFJAVOOONJE-ZIAGYGMSSA-N 0.000 description 2
- HAVYZKHVTLAPDZ-PRUKLFJYSA-N β-humulene Chemical compound C\C1=C\CC(C)(C)\C=C/CC(=C)CCC1 HAVYZKHVTLAPDZ-PRUKLFJYSA-N 0.000 description 2
- YKFLAYDHMOASIY-UHFFFAOYSA-N γ-terpinene Chemical compound CC(C)C1=CCC(C)=CC1 YKFLAYDHMOASIY-UHFFFAOYSA-N 0.000 description 2
- OPFTUNCRGUEPRZ-UHFFFAOYSA-N (+)-beta-Elemen Natural products CC(=C)C1CCC(C)(C=C)C(C(C)=C)C1 OPFTUNCRGUEPRZ-UHFFFAOYSA-N 0.000 description 1
- BQSLMQNYHVFRDT-CABCVRRESA-N (-)-gamma-Elemene Natural products CC(C)=C1CC[C@](C)(C=C)[C@@H](C(C)=C)C1 BQSLMQNYHVFRDT-CABCVRRESA-N 0.000 description 1
- BCTBAGTXFYWYMW-UHFFFAOYSA-N (3-R!)-2,2,6t-Trimethyl-6c-vinyl-tetrahydro-pyran-3r-ol Natural products CC1(C)OC(C)(C=C)CCC1O BCTBAGTXFYWYMW-UHFFFAOYSA-N 0.000 description 1
- IHPKGUQCSIINRJ-CSKARUKUSA-N (E)-beta-ocimene Chemical compound CC(C)=CC\C=C(/C)C=C IHPKGUQCSIINRJ-CSKARUKUSA-N 0.000 description 1
- DSSYKIVIOFKYAU-XCBNKYQSSA-N (R)-camphor Chemical compound C1C[C@@]2(C)C(=O)C[C@@H]1C2(C)C DSSYKIVIOFKYAU-XCBNKYQSSA-N 0.000 description 1
- BRHDDEIRQPDPMG-PSASIEDQSA-N (±)-cis-Linalyl oxide Chemical compound CC(C)(O)[C@H]1CC[C@@](C)(C=C)O1 BRHDDEIRQPDPMG-PSASIEDQSA-N 0.000 description 1
- VSMOENVRRABVKN-MRVPVSSYSA-N 1-Octen-3-ol Natural products CCCCC[C@H](O)C=C VSMOENVRRABVKN-MRVPVSSYSA-N 0.000 description 1
- XBGUIVFBMBVUEG-UHFFFAOYSA-N 1-methyl-4-(1,5-dimethyl-4-hexenylidene)-1-cyclohexene Chemical compound CC(C)=CCCC(C)=C1CCC(C)=CC1 XBGUIVFBMBVUEG-UHFFFAOYSA-N 0.000 description 1
- YDXQPTHHAPCTPP-UHFFFAOYSA-N 3-Octen-1-ol Natural products CCCCC=CCCO YDXQPTHHAPCTPP-UHFFFAOYSA-N 0.000 description 1
- SATQWIIUJKWZNO-UHFFFAOYSA-N 5-(3,3-dimethyloxiran-2-yl)-3-methylpent-1-en-3-ol Chemical compound C=CC(O)(C)CCC1OC1(C)C SATQWIIUJKWZNO-UHFFFAOYSA-N 0.000 description 1
- IKYKEVDKGZYRMQ-IUQGRGSQSA-N 9,12,15-Octadecatrien-1-ol Chemical compound CC\C=C\C\C=C\C\C=C\CCCCCCCCO IKYKEVDKGZYRMQ-IUQGRGSQSA-N 0.000 description 1
- NVEQFIOZRFFVFW-UHFFFAOYSA-N 9-epi-beta-caryophyllene oxide Natural products C=C1CCC2OC2(C)CCC2C(C)(C)CC21 NVEQFIOZRFFVFW-UHFFFAOYSA-N 0.000 description 1
- 241001647745 Banksia Species 0.000 description 1
- 235000002566 Capsicum Nutrition 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- YDDGKXBLOXEEMN-IABMMNSOSA-L Chicoric acid Natural products C1=C(O)C(O)=CC=C1\C=C\C(=O)O[C@@H](C([O-])=O)[C@H](C([O-])=O)OC(=O)\C=C\C1=CC=C(O)C(O)=C1 YDDGKXBLOXEEMN-IABMMNSOSA-L 0.000 description 1
- 235000008495 Chrysanthemum leucanthemum Nutrition 0.000 description 1
- 244000192528 Chrysanthemum parthenium Species 0.000 description 1
- 235000000604 Chrysanthemum parthenium Nutrition 0.000 description 1
- 241000723346 Cinnamomum camphora Species 0.000 description 1
- 244000018436 Coriandrum sativum Species 0.000 description 1
- 235000002787 Coriandrum sativum Nutrition 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- WEEGYLXZBRQIMU-WAAGHKOSSA-N Eucalyptol Chemical compound C1C[C@H]2CC[C@]1(C)OC2(C)C WEEGYLXZBRQIMU-WAAGHKOSSA-N 0.000 description 1
- 241000201295 Euphrasia Species 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- 239000006002 Pepper Substances 0.000 description 1
- 235000016761 Piper aduncum Nutrition 0.000 description 1
- 235000017804 Piper guineense Nutrition 0.000 description 1
- 244000203593 Piper nigrum Species 0.000 description 1
- 235000008184 Piper nigrum Nutrition 0.000 description 1
- 241000220317 Rosa Species 0.000 description 1
- KMJLGCYDCCCRHH-UHFFFAOYSA-N Spathulenol Natural products CC1(O)CCC2(C)C1C3C(CCC2=C)C3(C)C KMJLGCYDCCCRHH-UHFFFAOYSA-N 0.000 description 1
- 244000223014 Syzygium aromaticum Species 0.000 description 1
- 235000016639 Syzygium aromaticum Nutrition 0.000 description 1
- 150000007824 aliphatic compounds Chemical class 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- FAMPSKZZVDUYOS-UHFFFAOYSA-N alpha-Caryophyllene Natural products CC1=CCC(C)(C)C=CCC(C)=CCC1 FAMPSKZZVDUYOS-UHFFFAOYSA-N 0.000 description 1
- YHBUQBJHSRGZNF-HNNXBMFYSA-N alpha-bisabolene Natural products CC(C)=CCC=C(C)[C@@H]1CCC(C)=CC1 YHBUQBJHSRGZNF-HNNXBMFYSA-N 0.000 description 1
- QDUJKDRUFBJYSQ-UHFFFAOYSA-N alpha-elemene Natural products CC(C)C1=CC(=C(C)C)CCC1(C)C=C QDUJKDRUFBJYSQ-UHFFFAOYSA-N 0.000 description 1
- VYBREYKSZAROCT-UHFFFAOYSA-N alpha-myrcene Natural products CC(=C)CCCC(=C)C=C VYBREYKSZAROCT-UHFFFAOYSA-N 0.000 description 1
- 230000001754 anti-pyretic effect Effects 0.000 description 1
- 239000002221 antipyretic Substances 0.000 description 1
- NPNUFJAVOOONJE-UHFFFAOYSA-N beta-cariophyllene Natural products C1CC(C)=CCCC(=C)C2CC(C)(C)C21 NPNUFJAVOOONJE-UHFFFAOYSA-N 0.000 description 1
- 229930003493 bisabolene Natural products 0.000 description 1
- 229930008380 camphor Natural products 0.000 description 1
- 229960000846 camphor Drugs 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 229940117948 caryophyllene Drugs 0.000 description 1
- NPNUFJAVOOONJE-UONOGXRCSA-N caryophyllene Natural products C1CC(C)=CCCC(=C)[C@@H]2CC(C)(C)[C@@H]21 NPNUFJAVOOONJE-UONOGXRCSA-N 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 235000009508 confectionery Nutrition 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- FRMCCTDTYSRUBE-HYFYGGESSA-N ent-spathulenol Chemical compound C1CC(=C)[C@H]2CC[C@@](C)(O)[C@@H]2[C@H]2C(C)(C)[C@H]21 FRMCCTDTYSRUBE-HYFYGGESSA-N 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 235000008384 feverfew Nutrition 0.000 description 1
- -1 flavone compound Chemical class 0.000 description 1
- 235000013355 food flavoring agent Nutrition 0.000 description 1
- WTRAORJBWZMQIV-UHFFFAOYSA-N gamma-bisabolene Natural products CC(C)CCCC(C)=C1CCC(C)=CC1 WTRAORJBWZMQIV-UHFFFAOYSA-N 0.000 description 1
- BQSLMQNYHVFRDT-LSDHHAIUSA-N gamma-elemene Chemical compound CC(C)=C1CC[C@@](C)(C=C)[C@H](C(C)=C)C1 BQSLMQNYHVFRDT-LSDHHAIUSA-N 0.000 description 1
- RVOXATXFYDNXRE-UHFFFAOYSA-N gamma-elemene Natural products CC(=C1CCC(C)(C(C1)C(=C)C)C(=C)C)C RVOXATXFYDNXRE-UHFFFAOYSA-N 0.000 description 1
- 238000002290 gas chromatography-mass spectrometry Methods 0.000 description 1
- 239000001307 helium Substances 0.000 description 1
- 229910052734 helium Inorganic materials 0.000 description 1
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 description 1
- WBJNXHBNDYASJD-UHFFFAOYSA-N hexadec-7-yne Chemical compound CCCCCCCCC#CCCCCCC WBJNXHBNDYASJD-UHFFFAOYSA-N 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 210000004185 liver Anatomy 0.000 description 1
- 229930003658 monoterpene Natural products 0.000 description 1
- 150000002773 monoterpene derivatives Chemical class 0.000 description 1
- 235000002577 monoterpenes Nutrition 0.000 description 1
- 229940038384 octadecane Drugs 0.000 description 1
- 150000002924 oxiranes Chemical class 0.000 description 1
- 150000002926 oxygen Chemical class 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 208000011580 syndromic disease Diseases 0.000 description 1
- RBNWAMSGVWEHFP-UHFFFAOYSA-N trans-p-Menthane-1,8-diol Chemical compound CC(C)(O)C1CCC(C)(O)CC1 RBNWAMSGVWEHFP-UHFFFAOYSA-N 0.000 description 1
- 238000000870 ultraviolet spectroscopy Methods 0.000 description 1
- IHPKGUQCSIINRJ-UHFFFAOYSA-N β-ocimene Natural products CC(C)=CCC=C(C)C=C IHPKGUQCSIINRJ-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Fats And Perfumes (AREA)
Abstract
本发明公开了神农香菊叶的提取方法及其提取物在卷烟中的应用,属于烟用香料技术领域。神农香菊叶的提取方法按以下步骤依次进行:(1)粉碎成粗粉;(2)将神农香菊叶粗粉进行酶解;(3)将酶解后混合料液提取挥发油至完全,得到黄色透明油状物,将其溶解到乙醇中,得提取液A;(4)将提取挥发油的剩余混合料液过滤,滤出液挥干,得干浸膏;过滤残渣置于烘箱中低温烘干;(5)将上述干浸膏与残渣合并,对干浸膏和残渣回流提取所得即为提取香原料B。将提取液A按0.01-0.08%的比例进行加香;将提取香原料B制成溶液,以0.05-0.2%的比例进行加料。本发明方法简单,实施容易,能对卷烟产生良好的加香加料效果。
Description
技术领域
本发明属于烟用香料技术领域,具体涉及一种从废弃的神农香菊叶中提取香精香料的方法,及其提取物在卷烟中的应用。
背景技术
神农香菊叶为菊科植物神农香菊Dendranthema indicum(L)Des Monl.vararomaticum的干燥叶,“神农香菊”系菊科菊属(Dendranthema)的一个新变种,为神农架地区特有植物,具有平肝明目、清热解毒、散风降压的功效,民间作辛凉解表、清热药。因其具有特殊的浓郁香气,民间以其花、叶阴干作香囊。神农香菊花作为香原料已在卷烟中得到应用,但其叶一般废弃不用。对于神农香菊叶的开发研究,未见报道。
发明内容
针对现有技术的上述不足,本申请人要解决的技术问题是提供一种神农香菊叶的提取方法,从废物中提取了有用的宝物。本申请人要解决的另一技术问题是将提取物应用到卷烟中,使其产生良好的加香加料效果。
本发明的技术方案是:神农香菊叶的提取方法按以下步骤依次进行:
(1)将神农香菊叶粉碎成小于20目的粗粉;
(2)配制含有1~2%复合酶的pH为3.0~5.0的磷酸缓冲溶液,将神农香菊叶粗粉以1:12的比例添加到上述缓冲溶液中,水温40~50℃,进行酶解3~5小时;
(3)将酶解后的神农香菊叶混合料液进行水蒸汽蒸馏提取挥发油至完全,得到黄色透明油状物,将其溶解到100倍量的75%乙醇中,所得到的乙醇溶液即是神农香菊叶的提取液A;
(4)将提取挥发油的剩余混合料液过滤,滤出液90℃-100℃下加热挥发溶剂至干,得干浸膏;过滤残渣置于烘箱中低温烘干;
(5)将上述干浸膏与残渣合并,用其重量10~14倍量的60~95%乙醇作溶剂,对干浸膏和残渣回流提取2次,每次1.0~2.0小时,过滤,合并两次所得滤液,将滤液减压回收乙醇至小体积,浓缩至稠膏状,80℃-90℃下干燥,所得干物质即为神农香菊叶的提取香原料B。
所述的复合酶由纤维素酶和果胶酶组成,复合酶中纤维素酶:果胶酶=3:1。所述的纤维素酶和果胶酶为工业生产酶。
用上述方法提取的神农香菊叶提取物的应用,其特别之处在于:将神农香菊叶的提取液A按0.01-0.08%的比例添加到配方烟丝中进行加香;将神农香菊叶的提取香原料B按现有技术的方法加热制成溶液,以0.05-0.2%的比例添加到烟叶中进行加料。
本发明方法简单,实施容易,将废弃的神农香菊叶子加以利用,并能对卷烟产生良好的加香加料效果,成本低廉,使用方便,是一种绿色生产的积极措施。
具体实施方式
下面结合实施例对本发明的有关技术问题作进一步详细的描述。
本申请人通过研究发现,神农香菊叶的挥发油提取物和黄酮类提取物与其花具有相似的化学成分和香味特征,将其应用于卷烟中,可产生良好的加香加料效果,从而完成了本发明。本发明先用生物酶处理技术对神农香菊叶进行预处理,然后提取挥发油,再对其黄酮类化合物进行提取,选取了最佳工艺,充分提取了可用成分。本发明的方法简单实用,技术措施得当,充分提取了神农香菊叶中的可用成分挥发油提取物和黄酮类提取物。本发明的提取物具有与神农香菊花相似的化学成分和香味特征,将其应用于卷烟中,可产生良好的加香加料效果。
下面是本申请人提取工艺的几个实施例。
实施例1.
将神农香菊的花粉碎成小于20目的粗粉,用PH为3.5的磷酸缓冲溶液配制含有1.0%的复合酶溶液,纤维素酶:果胶酶=3:1;将粉碎成粗粉的神农香菊叶5千克以1:12的比例添加该溶液,水温控制在40±0.5℃,进行酶解3.5小时;将酶解后的神农香菊叶混合料液进行水蒸汽蒸馏提取挥发油至完全,得到黄色透明油状物,将其溶解到100倍量的75%乙醇中,得到提取液A;将剩余混合料液过滤,滤出液挥干,得干浸膏,残渣置于烘箱中低温烘干,干浸膏与残渣合并,用8倍量95%乙醇作溶剂,回流提取2次,每次提1.5小时,滤过,合并两次所得滤液,减压回收乙醇至小体积,浓缩至稠膏状,干燥,即得提取香原料B;
实施例2.
将神农香菊的花粉碎成小于20目的粗粉,用PH为4.5的磷酸缓冲溶液配制含有1.2%的复合酶溶液,纤维素酶:果胶酶=3:1;将粉碎成粗粉的神农香菊叶5千克以1:12的比例添加该溶液,水温控制在40±0.5℃,进行酶解5.0小时;将酶解后的神农香菊叶混合料液进行水蒸汽蒸馏提取挥发油至完全,得到黄色透明油状物,将其溶解到100倍量的75%乙醇中,得到提取液A;将剩余混合料液过滤,滤出液挥干,得干浸膏,残渣置于烘箱中低温烘干,干浸膏与残渣合并,用12倍量95%乙醇作溶剂,回流提取2次,每次提1.0小时,滤过,合并两次所得滤液,减压回收乙醇至小体积,浓缩至稠膏状,干燥,即得提取香原料B;
实施例3.
将神农香菊的花粉碎成小于20目的粗粉,用PH为5.0的磷酸缓冲溶液配制含有1.5%的复合酶溶液,纤维素酶:果胶酶=3:1;将粉碎成粗粉的神农香菊叶5千克以1:12的比例添加该溶液,水温控制在40±0.5℃,进行酶解4.0小时;将酶解后的神农香菊叶混合料液进行水蒸汽蒸馏提取挥发油至完全,得到黄色透明油状物,将其溶解到100倍量的75%乙醇中,得到提取液A;将剩余混合料液过滤,滤出液挥干,得干浸膏,残渣置于烘箱中低温烘干,干浸膏与残渣合并,用12倍量70%乙醇作溶剂,回流提取2次,每次提1.5小时,滤过,合并两次所得滤液,减压回收乙醇至小体积,浓缩至稠膏状,干燥,即得提取香原料B;
实施例4.
将神农香菊的花粉碎成小于20目的粗粉,用PH为3.0的磷酸缓冲溶液配制含有2.0%的复合酶溶液,纤维素酶:果胶酶=3:1;将粉碎成粗粉的神农香菊叶5千克以1:12的比例添加该溶液,水温控制在40±0.5℃,进行酶解3.0小时;将酶解后的神农香菊叶混合料液进行水蒸汽蒸馏提取挥发油至完全,得到黄色透明油状物,将其溶解到100倍量的75%乙醇中,得到提取液A;将剩余混合料液过滤,滤出液挥干,残渣置于烘箱中低温烘干,干浸膏与残渣合并,用10倍量70%乙醇作溶剂,回流提取2次,每次提2.0小时,滤过,合并两次所得滤液,减压回收乙醇至小体积,浓缩至稠膏状,干燥,即得提取香原料B;
实施例5.
将神农香菊的花粉碎成小于20目的粗粉,用PH为4.0的磷酸缓冲溶液配制含有1.8%的复合酶溶液,纤维素酶:果胶酶=3:1;将粉碎成粗粉的神农香菊叶5千克以1:12的比例添加该溶液,水温控制在40±0.5℃,进行酶解4.0小时;将酶解后的神农香菊叶混合料液进行水蒸汽蒸馏提取挥发油至完全,得到黄色透明油状物,将其溶解到100倍量的75%乙醇中,得到提取液A;将剩余混合料液过滤,滤出液挥干,得干浸膏,残渣置于烘箱中低温烘干,干浸膏与残渣合并,用10倍量60%乙醇作溶剂,回流提取2次,每次提1.5小时,滤过,合并两次所得滤液,减压回收乙醇至小体积,浓缩至稠膏状,干燥,即得提取香原料B;
本申请人对神农香菊提取液A进行了分析测定,具体结果如下:
气质联用仪分析方法:分别取供试品溶液3μL,进行GC-MS分析,分析条件为:色谱柱:DB-WAX(30m×0.32mm×0.25μm)石英毛细管柱;程序升温:60℃,保持3分钟,先以3℃/分钟升温至120℃,再以1℃/分钟升温至140℃,保持3min,最后以8℃/分钟升温至240℃,保持5分钟;进样口温度250℃;载气:99.999%氦气;载气流速:1.2mL/min;分流比30:1;溶剂延时3min。质谱条件:离子源:EI源;离子源温度:230℃;四级杆温度:150℃;电子能量:70eV;倍增管电压:1.2KV;接口温度:250℃;质量扫描范围30-450amu。
分析结果:通过HP MSD化学工作站检索NIST标准质谱图库,同时结合有关质谱图文献解析,寻找神农香菊叶挥发油中特征香成分。按各峰的质谱图经计算机质谱数据库检索,并按各峰的质谱裂片图与文献资料核对,确定了其中57个组分,其中有36种特征香成分与神农香菊花的一致(见表1)。
由表可知,神农香菊叶挥发性成分主要为单萜、倍半萜类及其含氧衍生物和脂肪族化合物等烟叶香气物质的重要前体物;另外芳樟醇具有似芫荽香气,增加烟气的木香与青香;松油醇是烟草中本身含有的制香物质,对卷烟的吸味有着重要的影响,具有松针香气;桉树脑是重要的烟草天然味香成分,可以赋予卷烟新鲜、樟脑样和胡椒样的吸味;丁香子酚是现在卷烟加香常用的香味成分,赋予卷烟辛甜气息;这些成分与香气前提物质共同构成了提取液A的特征香气。
表1 提取液A中与神农香菊花挥发油一致的成分表
编号 | 化合物名称 | 化学式 |
1 | α-Phellandrene,α-水芹烯 | C10H16 |
2 | cis-Linalool oxide,顺-芳樟醇氧化物 | C10H18O2 |
3 | 3,7-dimethyl-1,6-Octadien-3-ol,芳樟醇 | C10H18O |
4 | Verbenone,马鞭草烯酮 | C10H14O |
5 | Spathulenol,匙叶桉油烯醇 | C15H24O |
6 | 2,2’-methylenebis[6-(1,1-dimethylethyl)-4-methyl-Phenol,2,2’-二亚甲基二[6-(1,1-二甲基乙基)-4-甲基-苯酚 | C23H32O2 |
7 | α-Terpineol,α-松油醇 | C10H18O |
8 | n-Decanoic acid,正癸酸 | C10H20O2 |
9 | n-Hexadecanoic acid,十六烷酸 | C16H32O2 |
10 | cis-Linaloloxide,顺-芳樟醇氧化物 | C10H18O2 |
11 | 4-Acetyl-1-methylcyclohexene,4-乙酰基-1-甲基-环己烯 | C9H14O |
12 | 3-Methyl-4-isopropylphenol,3-甲基-4-异丙基苯酚 | C10H14O |
13 | Eugenol,丁子香酚 | C10H12O2 |
14 | Caryophyllene,石竹烯 | C15H24 |
15 | 7,11-dimethyl-3-methylene-1,6,10-Dodecatriene,7,11-二甲基-3-亚甲基-1,6,10-十二碳三烯 | C15H24 |
16 | γ-Elemene,γ-榄烯 | C15H24 |
17 | 7-Hexadecyne,7-十六炔 | C16H30 |
18 | 9,12,15-Octadecatrien-1-ol,9,12,15-十八烷二亚乙基四胺-1醇 | C18H32O |
19 | Hexadecane,十六烷 | C16H34 |
20 | Nonadecane,十九烷 | C19H40 |
21 | Butanoic acid-2-methyl-propyl ester,丁酸-2-甲基丙酯 | C8H16O2 |
22 | Benzaldehyde,苯甲醛 | C7H6O |
23 | Myrcene,月桂烯 | C10H16 |
24 | 1-Octen-3-ol,1-辛烯-3-醇 | C8H16O |
25 | β-Phellandrene,β-水芹烯 | C8H16 |
26 | Eucalyptol,桉树脑 | C10H18O |
27 | β-ocimene,β-罗勒烯 | C10H16 |
28 | cis-Bisabolene epoxide,顺-环氧红没药烯 | C15H24O |
29 | γ-Terpinene,γ-松油烯 | C10H16 |
30 | (+)-4-Carene,(+)-4-蒈烯 | C10H16 |
31 | 2,4-Decadienal,2,4-癸二烯醛 | C10H16O |
32 | 2,6,6,9-tetramethyl-tricyclo[5.4.0.0(2,8)]-undec-9-ene,2,6,6,9-四甲基-三环[5.4.0.0(2.8)]-十一碳-9-烯 | C15H24 |
33 | Methyl cinnamate,肉桂酸甲酯 | C10H10O2 |
34 | β-sesquiphellandrene,β-倍半水芹烯 | C15H24 |
35 | Thujopsene,罗汉柏烯 | C15H24 |
36 | β-Humulene,β-律草烯 | C15H24 |
申请人对提取物B进行了分析测定,具体结果如下:
浸膏得率的测定:精密量取供试品溶液20mL,至干燥至恒重的蒸发皿上,于水浴上蒸干,在105℃干燥3h,移至干燥器中冷却1h,迅速称定重量,计算浸膏得率。
有效成分含量的测定:总黄酮的测定方法参照《中国药典》2005年版一部附录VA之紫外-可见分光光度法。
结果分析:以干浸膏得率为考察指标,影响提取效果的因素顺序为:乙醇浓度>乙醇用量>回流时间。经方差分析,乙醇浓度对干浸膏得率有显著性影响。以总黄酮得率为考察指标,影响提取效果的因素顺序为:乙醇浓度>乙醇用量>回流时间。经方差分析,乙醇浓度对总黄酮得率有显著性影响。神农香菊叶(除油)总黄酮提取物的最佳提取工艺为:用10倍量95%乙醇作溶剂,回流提取2次,每次1.5小时,在最佳工艺条件下神农香菊(除油)总黄酮提取物的浸膏得率为9.30±0.05%,总黄酮含量为4.50±0.21%,在相同条件下,我们对神农香菊花进行提取,其浸膏得率为14.10±0.05%,总黄酮含量为6.50±0.20%,由此可见,神农香菊叶的浸膏得率和提取物中总黄酮的含量比较接近神农香菊,如能对神农香菊叶进行提取利用,可大大降低神农香菊烟用香原料的成本。
本申请人用中档空白(未加料加香)烟丝,采用提取液A和B组合应用加香加料,并对样品卷烟进行了评吸对比实验。空白卷烟是用同样方式处理的加入等量的稀释溶剂的卷烟,表上所标示的施加量是空白卷烟和本发明的烟用提取物均采用的加香或者加料的比例。本实验方案中只是列举单独使用的效果,还可根据具体的烟丝配方进行两种提取物的组合应用。
根据评吸结果,提取液A在表现淡雅风格方面及柔和烟气、增加顺畅感、改善口感方面有比较明显效果,能与卷烟本草香互相提携,并且其用量低,但用量到0.08%后,香气有所压抑。适合用量0.01-0.08%。
表2、提取液A在卷烟中的应用
表3、提取物B在卷烟中的应用
根据评吸结果,可以看出提取物B在表现淡雅风格方面不突出,对柔和烟气、增加顺畅感、改善口感方面效果比较明显,但最大用量到0.5%后,香气有所压抑。适合用量0.05-0.2%。
同时,我们对相同条件下提取的神农香菊花的提取物也进行了感官评吸,根据评吸结果,花的提取液A在表现淡雅风格方面突出,对柔和烟气、增加顺畅感、改善口感方面有比较明显效果,能与卷烟本草香互相提携;而花的提取物B具有增香效果,同时在烟气中能较完美的揉合神农香菊所独具的特殊香气,赋予卷烟淡雅风格。由此可见,神农香菊的叶和花的提取物不仅在成分上有大致相同之处,在卷烟中应用后的感官评价结果也有相同之处,它们都能对卷烟产生良好的评吸效果,如增香、柔和烟气、改善口感等,因此,神农香菊叶的提取物在卷烟中的应用也极具开发价值。
Claims (3)
1.一种神农香菊叶的提取方法,其特征在于所述的提取方法按以下步骤依次进行:
(1)将神农香菊叶粉碎成小于20目的粗粉;
(2)配制含有1~2%复合酶的pH为3.0~5.0的磷酸缓冲溶液,将神农香菊叶粗粉以1∶12的比例添加到上述缓冲溶液中,水温40~50℃,进行酶解3~5小时;所述复合酶由纤维素酶和果胶酶组成,复合酶中纤维素酶∶果胶酶=3∶1;
(3)将酶解后的神农香菊叶混合料液进行水蒸汽蒸馏提取挥发油至完全,得到黄色透明油状物,将其溶解到100倍量的75%乙醇中,所得到的乙醇溶液即是神农香菊叶的提取液A;
(4)将提取挥发油的剩余混合料液过滤,滤出液90℃-100℃下加热挥发溶剂至干,得干浸膏;过滤残渣置于烘箱中低温烘干;
(5)将上述干浸膏与残渣合并,用其重量10~14倍量的60~95%乙醇作溶剂,对干浸膏和残渣回流提取2次,每次1.0~2.0小时,过滤,合并两次所得滤液,将滤液减压回收乙醇至小体积,浓缩至稠膏状,80℃-90℃下干燥,所得到的干物质即为神农香菊叶的提取香原料B。
2.根据权利要求1所述的神农香菊叶的提取方法,其特征在于:所述的纤维素酶和果胶酶为工业生产酶。
3.一种用权利要求1方法提取的神农香菊叶提取物在卷烟中的应用,其特征在于:将神农香菊叶的提取液A按0.01-0.08%的比例添加到配方烟丝中进行加香;将神农香菊叶的提取香原料B按现有技术的方法加热制成溶液,以0.05-0.2%的比例添加到烟叶中进行加料。
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN2008101975376A CN101731748B (zh) | 2008-11-05 | 2008-11-05 | 神农香菊叶的提取方法及其提取物在卷烟中的应用 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN2008101975376A CN101731748B (zh) | 2008-11-05 | 2008-11-05 | 神农香菊叶的提取方法及其提取物在卷烟中的应用 |
Publications (2)
Publication Number | Publication Date |
---|---|
CN101731748A CN101731748A (zh) | 2010-06-16 |
CN101731748B true CN101731748B (zh) | 2012-07-18 |
Family
ID=42456164
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN2008101975376A Active CN101731748B (zh) | 2008-11-05 | 2008-11-05 | 神农香菊叶的提取方法及其提取物在卷烟中的应用 |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN101731748B (zh) |
Families Citing this family (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101928642B (zh) * | 2010-06-22 | 2012-10-03 | 武汉神农天香生物科技有限公司 | 一种植物神农香菊的全草中提取分离香料和药用成分的方法 |
CN101889728B (zh) * | 2010-07-03 | 2012-07-18 | 中国烟草总公司郑州烟草研究院 | 一种乙醇提取烘烤发酵麦芽浸膏的方法及其在烟草中的应用 |
CN102423112A (zh) * | 2011-07-23 | 2012-04-25 | 云南烟草科学研究院 | 松油醇溶液在卷烟烟丝中的应用 |
CN102827693B (zh) * | 2012-08-16 | 2013-10-09 | 湖北中烟工业有限责任公司 | 烟用花香香韵香精 |
CN102823939B (zh) * | 2012-09-17 | 2016-03-30 | 福建中烟工业有限责任公司 | 一种野茄子叶提取液的制备方法及其在卷烟中的应用 |
CN103060091A (zh) * | 2012-12-14 | 2013-04-24 | 湖北中烟工业有限责任公司 | 毛蕊花提取物的制备方法 |
CN103070475B (zh) * | 2013-01-10 | 2015-05-20 | 川渝中烟工业有限责任公司 | 雪茄烟叶添加剂及其生产方法 |
CN103211297B (zh) * | 2013-04-03 | 2015-04-08 | 红云红河烟草(集团)有限责任公司 | 一种猕猴桃提取物的制备方法及其在卷烟中的应用 |
CN103211290A (zh) * | 2013-05-13 | 2013-07-24 | 湖北中烟工业有限责任公司 | 提高全梗再造烟叶质量的方法 |
CN103361174B (zh) * | 2013-07-29 | 2014-11-26 | 湖北中烟工业有限责任公司 | 一种茵陈烟用香料及其制备方法 |
CN104382226B (zh) * | 2014-11-11 | 2017-02-15 | 湖北中烟工业有限责任公司 | 一种白肋烟精提物的制备方法 |
CN105001993A (zh) * | 2015-07-17 | 2015-10-28 | 王再青 | 一种提高檀香精油提取率的方法 |
CN105287676A (zh) * | 2015-10-26 | 2016-02-03 | 湖北来凤腾升香料化工有限公司 | 一种用微波辅助制备来凤香菊浸膏的酶解方法 |
CN105176692A (zh) * | 2015-10-26 | 2015-12-23 | 湖北来凤腾升香料化工有限公司 | 一种用微波辅助制备来凤香菊精油的酶解方法 |
CN105602729A (zh) * | 2015-11-23 | 2016-05-25 | 江西中烟工业有限责任公司 | 一种郁金香香精的提取方法 |
CN108546594A (zh) * | 2018-04-12 | 2018-09-18 | 江西中烟工业有限责任公司 | 一种泥蒿烟用香料的制备方法和应用 |
CN108264965B (zh) * | 2018-04-12 | 2021-06-08 | 江西中烟工业有限责任公司 | 一种泥蒿酶解提取物的制备方法及其在卷烟中的应用 |
CN109875018A (zh) * | 2018-10-31 | 2019-06-14 | 华宝香精股份有限公司 | 一种结合dhpm及酶解技术制备大青叶香精的方法 |
CN113633019B (zh) * | 2020-05-11 | 2023-04-28 | 中国烟草总公司郑州烟草研究院 | 一种雪茄风味烟草提取物及其制备方法 |
CN114681650B (zh) * | 2020-12-30 | 2024-05-07 | 象鼻山香(杭州)生物科技有限公司 | 一种具有除臭功能的组合物及其制备方法 |
Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1749379A (zh) * | 2005-10-18 | 2006-03-22 | 中南大学 | 从柑桔类果皮中提取桔子油和果胶的方法 |
CN1837201A (zh) * | 2006-02-21 | 2006-09-27 | 张守政 | 从茶叶中提取茶多酚、茶氨酸、茶多糖、茶色素的方法 |
CN1875794A (zh) * | 2006-07-04 | 2006-12-13 | 云南瑞升烟草技术(集团)有限公司 | 烟用功能添加剂及其制备方法 |
CN101016559A (zh) * | 2007-01-13 | 2007-08-15 | 方佳洪 | 生产薯蓣皂素的零排方法 |
CN101204249A (zh) * | 2007-12-11 | 2008-06-25 | 广东中烟工业公司 | 一种烟草浸膏的制备方法 |
CN101229211A (zh) * | 2008-01-31 | 2008-07-30 | 广东药学院 | 一种西兰花种子提取物及其制备方法 |
CN101270142A (zh) * | 2008-04-17 | 2008-09-24 | 大连大学 | 油茶皂素的制备方法 |
-
2008
- 2008-11-05 CN CN2008101975376A patent/CN101731748B/zh active Active
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1749379A (zh) * | 2005-10-18 | 2006-03-22 | 中南大学 | 从柑桔类果皮中提取桔子油和果胶的方法 |
CN1837201A (zh) * | 2006-02-21 | 2006-09-27 | 张守政 | 从茶叶中提取茶多酚、茶氨酸、茶多糖、茶色素的方法 |
CN1875794A (zh) * | 2006-07-04 | 2006-12-13 | 云南瑞升烟草技术(集团)有限公司 | 烟用功能添加剂及其制备方法 |
CN101016559A (zh) * | 2007-01-13 | 2007-08-15 | 方佳洪 | 生产薯蓣皂素的零排方法 |
CN101204249A (zh) * | 2007-12-11 | 2008-06-25 | 广东中烟工业公司 | 一种烟草浸膏的制备方法 |
CN101229211A (zh) * | 2008-01-31 | 2008-07-30 | 广东药学院 | 一种西兰花种子提取物及其制备方法 |
CN101270142A (zh) * | 2008-04-17 | 2008-09-24 | 大连大学 | 油茶皂素的制备方法 |
Also Published As
Publication number | Publication date |
---|---|
CN101731748A (zh) | 2010-06-16 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN101731748B (zh) | 神农香菊叶的提取方法及其提取物在卷烟中的应用 | |
Rao et al. | Water soluble fractions of rose-scented geranium (Pelargonium species) essential oil | |
Farsam et al. | Composition of the essential oils of wild and cultivated Satureja khuzistanica Jamzad from Iran | |
Chamorro et al. | Study of the chemical composition of essential oils by gas chromatography | |
Rao et al. | Chemical profiles of primary and secondary essential oils of palmarosa (Cymbopogon martinii (Roxb.) Wats var. motia Burk.) | |
Zoghbi et al. | Volatile constituents from leaves and flowers of Alpinia speciosa K. Schum. and A. purpurata (Viell.) Schum. | |
Ahmad et al. | Extraction, separation and identification of chemical ingredients of Elephantopus scaber L. using factorial design of experiment | |
Khan et al. | Determination of chemical constituents of leaf and stem essential oils of Artemisia monosperma from central Saudi Arabia | |
Hassanpouraghdam et al. | Essential oil constituents of Lavandula officinalis Chaix. from Northwest Iran | |
Shamspur et al. | The effects of onion and salt treatments on essential oil content and composition of Rosa damascena Mill | |
Kuiate et al. | Chemical composition and antidermatophytic properties of volatile fractions of hexanic extract from leaves of Cupressus lusitanica Mill. from Cameroon | |
Rana et al. | Chemical constituents of the volatile oil of Murraya koenigii leaves | |
Uraku | Leaves by gas chromatography-mass spectrometry (GC-MS) method | |
Zhu et al. | Comparative studies on flavor substances of leaves and pericarps of Zanthoxylum bungeanum Maxim. at different harvest periods | |
Khan et al. | Essential oil composition of Taxus wallichiana Zucc. from the Northern Himalayan region of India | |
Gretšušnikova et al. | Comparative analysis of the composition of the essential oil from the shoots, leaves and stems the wild Ledum palustre L. from Estonia | |
Lal et al. | Identification of a stable rhizome essential oil-rich variety (Jor Lab SM-2) of Homalomena aromatica schott., through biometrical method | |
Bhardwaj et al. | Effect of seasonal variation on chemical composition and physicochemical properties of Hedychium spicatum rhizomes essential oil | |
Lago et al. | Microclimatic factors and phenology influences in the chemical composition of the essential oils from Pittosporum undulatum Vent. leaves | |
Rout et al. | Comparison of extraction methods of Mimusops elengi L. flowers | |
KR101694484B1 (ko) | 한방 꽃의 향취를 재현한 향료 조성물 | |
KR20120109021A (ko) | 감국꽃의 향취를 재현한 향료 조성물 및 이를 함유하는 피부 외용제 조성물 | |
Angmor et al. | Studies on Cinnamomum zeylanicum–part I. The essential oil components of C. Zeylanicum nees grown in Ghana | |
Hu et al. | Variations in volatile oil yields and compositions of Magnolia zenii Cheng flower buds at different growth stages | |
CN114041623B (zh) | 一种旱烟特征致香成分、其制备方法和用途 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
C14 | Grant of patent or utility model | ||
GR01 | Patent grant |