CA2026539C - Cigarette and smokable filler material therefor - Google Patents
Cigarette and smokable filler material thereforInfo
- Publication number
- CA2026539C CA2026539C CA002026539A CA2026539A CA2026539C CA 2026539 C CA2026539 C CA 2026539C CA 002026539 A CA002026539 A CA 002026539A CA 2026539 A CA2026539 A CA 2026539A CA 2026539 C CA2026539 C CA 2026539C
- Authority
- CA
- Canada
- Prior art keywords
- filler
- cigarette
- smokable
- component
- tobacco
- 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.)
- Expired - Fee Related
Links
- 239000000463 material Substances 0.000 title claims abstract description 321
- 239000000945 filler Substances 0.000 title claims abstract description 222
- 235000019504 cigarettes Nutrition 0.000 title claims abstract description 132
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims abstract description 132
- 235000002637 Nicotiana tabacum Nutrition 0.000 claims abstract description 119
- 239000011159 matrix material Substances 0.000 claims abstract description 84
- 239000002245 particle Substances 0.000 claims abstract description 68
- 229910000019 calcium carbonate Inorganic materials 0.000 claims abstract description 61
- 229920000615 alginic acid Polymers 0.000 claims abstract description 43
- 235000010443 alginic acid Nutrition 0.000 claims abstract description 42
- FHVDTGUDJYJELY-UHFFFAOYSA-N 6-{[2-carboxy-4,5-dihydroxy-6-(phosphanyloxy)oxan-3-yl]oxy}-4,5-dihydroxy-3-phosphanyloxane-2-carboxylic acid Chemical compound O1C(C(O)=O)C(P)C(O)C(O)C1OC1C(C(O)=O)OC(OP)C(O)C1O FHVDTGUDJYJELY-UHFFFAOYSA-N 0.000 claims abstract description 39
- 229940072056 alginate Drugs 0.000 claims abstract description 38
- 239000000443 aerosol Substances 0.000 claims abstract description 34
- 239000011230 binding agent Substances 0.000 claims abstract description 27
- 239000000284 extract Substances 0.000 claims abstract description 16
- 241000208125 Nicotiana Species 0.000 claims abstract 19
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 36
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 18
- 239000011256 inorganic filler Substances 0.000 claims description 12
- 229910003475 inorganic filler Inorganic materials 0.000 claims description 12
- 235000010407 ammonium alginate Nutrition 0.000 claims description 11
- 239000000728 ammonium alginate Substances 0.000 claims description 11
- KPGABFJTMYCRHJ-YZOKENDUSA-N ammonium alginate Chemical compound [NH4+].[NH4+].O1[C@@H](C([O-])=O)[C@@H](OC)[C@H](O)[C@H](O)[C@@H]1O[C@@H]1[C@@H](C([O-])=O)O[C@@H](O)[C@@H](O)[C@H]1O KPGABFJTMYCRHJ-YZOKENDUSA-N 0.000 claims description 11
- 239000011872 intimate mixture Substances 0.000 claims description 11
- 230000015572 biosynthetic process Effects 0.000 claims description 10
- 235000011187 glycerol Nutrition 0.000 claims description 9
- 239000004088 foaming agent Substances 0.000 claims description 3
- MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 claims description 2
- 244000061176 Nicotiana tabacum Species 0.000 description 100
- 239000000203 mixture Substances 0.000 description 57
- 239000002002 slurry Substances 0.000 description 47
- 238000000034 method Methods 0.000 description 28
- 239000000779 smoke Substances 0.000 description 28
- 239000000796 flavoring agent Substances 0.000 description 24
- 230000000391 smoking effect Effects 0.000 description 20
- 239000007921 spray Substances 0.000 description 15
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 14
- 239000003575 carbonaceous material Substances 0.000 description 14
- 239000008399 tap water Substances 0.000 description 14
- 235000020679 tap water Nutrition 0.000 description 14
- 239000003795 chemical substances by application Substances 0.000 description 13
- 235000013355 food flavoring agent Nutrition 0.000 description 13
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 12
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 10
- 238000004519 manufacturing process Methods 0.000 description 10
- 235000019634 flavors Nutrition 0.000 description 9
- -1 polypropylene Polymers 0.000 description 9
- 229940088417 precipitated calcium carbonate Drugs 0.000 description 9
- 239000007787 solid Substances 0.000 description 9
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 8
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- 229910002092 carbon dioxide Inorganic materials 0.000 description 7
- 230000035699 permeability Effects 0.000 description 7
- 239000000243 solution Substances 0.000 description 7
- BHPQYMZQTOCNFJ-UHFFFAOYSA-N Calcium cation Chemical compound [Ca+2] BHPQYMZQTOCNFJ-UHFFFAOYSA-N 0.000 description 6
- 229910001424 calcium ion Inorganic materials 0.000 description 6
- 150000004676 glycans Chemical class 0.000 description 6
- 229920001903 high density polyethylene Polymers 0.000 description 6
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- 235000010987 pectin Nutrition 0.000 description 6
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- 239000005017 polysaccharide Substances 0.000 description 6
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 6
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- 238000002485 combustion reaction Methods 0.000 description 5
- 239000007789 gas Substances 0.000 description 5
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- 239000011368 organic material Substances 0.000 description 5
- 238000002360 preparation method Methods 0.000 description 5
- 150000003839 salts Chemical class 0.000 description 5
- NOOLISFMXDJSKH-UTLUCORTSA-N (+)-Neomenthol Chemical compound CC(C)[C@@H]1CC[C@@H](C)C[C@@H]1O NOOLISFMXDJSKH-UTLUCORTSA-N 0.000 description 4
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 4
- 241000581364 Clinitrachus argentatus Species 0.000 description 4
- NOOLISFMXDJSKH-UHFFFAOYSA-N DL-menthol Natural products CC(C)C1CCC(C)CC1O NOOLISFMXDJSKH-UHFFFAOYSA-N 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- 241000202807 Glycyrrhiza Species 0.000 description 4
- 235000001453 Glycyrrhiza echinata Nutrition 0.000 description 4
- 235000006200 Glycyrrhiza glabra Nutrition 0.000 description 4
- 235000017382 Glycyrrhiza lepidota Nutrition 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- 235000009470 Theobroma cacao Nutrition 0.000 description 4
- 244000299461 Theobroma cacao Species 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 4
- 239000012298 atmosphere Substances 0.000 description 4
- 239000001110 calcium chloride Substances 0.000 description 4
- 229910001628 calcium chloride Inorganic materials 0.000 description 4
- 239000001768 carboxy methyl cellulose Substances 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- 239000000835 fiber Substances 0.000 description 4
- 239000000446 fuel Substances 0.000 description 4
- 229940010454 licorice Drugs 0.000 description 4
- 229940041616 menthol Drugs 0.000 description 4
- 235000013379 molasses Nutrition 0.000 description 4
- 238000012856 packing Methods 0.000 description 4
- 235000013772 propylene glycol Nutrition 0.000 description 4
- 239000002356 single layer Substances 0.000 description 4
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 3
- 239000001856 Ethyl cellulose Substances 0.000 description 3
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
- DPXJVFZANSGRMM-UHFFFAOYSA-N acetic acid;2,3,4,5,6-pentahydroxyhexanal;sodium Chemical compound [Na].CC(O)=O.OCC(O)C(O)C(O)C(O)C=O DPXJVFZANSGRMM-UHFFFAOYSA-N 0.000 description 3
- 159000000007 calcium salts Chemical class 0.000 description 3
- 150000001720 carbohydrates Chemical class 0.000 description 3
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 239000000428 dust Substances 0.000 description 3
- 235000019325 ethyl cellulose Nutrition 0.000 description 3
- 229920001249 ethyl cellulose Polymers 0.000 description 3
- 239000010410 layer Substances 0.000 description 3
- 239000000395 magnesium oxide Substances 0.000 description 3
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 3
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 3
- 229910000027 potassium carbonate Inorganic materials 0.000 description 3
- 235000019812 sodium carboxymethyl cellulose Nutrition 0.000 description 3
- MWOOGOJBHIARFG-UHFFFAOYSA-N vanillin Chemical compound COC1=CC(C=O)=CC=C1O MWOOGOJBHIARFG-UHFFFAOYSA-N 0.000 description 3
- FGQOOHJZONJGDT-UHFFFAOYSA-N vanillin Natural products COC1=CC(O)=CC(C=O)=C1 FGQOOHJZONJGDT-UHFFFAOYSA-N 0.000 description 3
- 235000012141 vanillin Nutrition 0.000 description 3
- 238000009736 wetting Methods 0.000 description 3
- JOOXCMJARBKPKM-UHFFFAOYSA-N 4-oxopentanoic acid Chemical compound CC(=O)CCC(O)=O JOOXCMJARBKPKM-UHFFFAOYSA-N 0.000 description 2
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical group [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- 240000008886 Ceratonia siliqua Species 0.000 description 2
- 235000013912 Ceratonia siliqua Nutrition 0.000 description 2
- 229920002907 Guar gum Polymers 0.000 description 2
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- 229920000161 Locust bean gum Polymers 0.000 description 2
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 2
- HDSBZMRLPLPFLQ-UHFFFAOYSA-N Propylene glycol alginate Chemical compound OC1C(O)C(OC)OC(C(O)=O)C1OC1C(O)C(O)C(C)C(C(=O)OCC(C)O)O1 HDSBZMRLPLPFLQ-UHFFFAOYSA-N 0.000 description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 238000013019 agitation Methods 0.000 description 2
- 150000001450 anions Chemical class 0.000 description 2
- 238000001354 calcination Methods 0.000 description 2
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- 238000005266 casting Methods 0.000 description 2
- 239000003610 charcoal Substances 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 239000000686 essence Substances 0.000 description 2
- 239000006260 foam Substances 0.000 description 2
- 235000010417 guar gum Nutrition 0.000 description 2
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- 229960002154 guar gum Drugs 0.000 description 2
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 2
- 230000003993 interaction Effects 0.000 description 2
- 150000002500 ions Chemical class 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 235000010420 locust bean gum Nutrition 0.000 description 2
- 239000000711 locust bean gum Substances 0.000 description 2
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 2
- 239000001095 magnesium carbonate Substances 0.000 description 2
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 2
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 2
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- 235000010482 polyoxyethylene sorbitan monooleate Nutrition 0.000 description 2
- SCVFZCLFOSHCOH-UHFFFAOYSA-M potassium acetate Chemical compound [K+].CC([O-])=O SCVFZCLFOSHCOH-UHFFFAOYSA-M 0.000 description 2
- 235000010409 propane-1,2-diol alginate Nutrition 0.000 description 2
- 239000000770 propane-1,2-diol alginate Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000012798 spherical particle Substances 0.000 description 2
- 235000000346 sugar Nutrition 0.000 description 2
- URAYPUMNDPQOKB-UHFFFAOYSA-N triacetin Chemical compound CC(=O)OCC(OC(C)=O)COC(C)=O URAYPUMNDPQOKB-UHFFFAOYSA-N 0.000 description 2
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 description 1
- IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical compound CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 description 1
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- 238000004438 BET method Methods 0.000 description 1
- BCZXFFBUYPCTSJ-UHFFFAOYSA-L Calcium propionate Chemical compound [Ca+2].CCC([O-])=O.CCC([O-])=O BCZXFFBUYPCTSJ-UHFFFAOYSA-L 0.000 description 1
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- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- SWESETWDPGZBCR-UHFFFAOYSA-N Ethylvanillin glucoside Chemical compound CCOC1=CC(C=O)=CC=C1OC1C(O)C(O)C(O)C(CO)O1 SWESETWDPGZBCR-UHFFFAOYSA-N 0.000 description 1
- 229930091371 Fructose Natural products 0.000 description 1
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- RJDOZRNNYVAULJ-UHFFFAOYSA-L [O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[F-].[F-].[Mg++].[Mg++].[Mg++].[Al+3].[Si+4].[Si+4].[Si+4].[K+] Chemical compound [O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[F-].[F-].[Mg++].[Mg++].[Mg++].[Al+3].[Si+4].[Si+4].[Si+4].[K+] RJDOZRNNYVAULJ-UHFFFAOYSA-L 0.000 description 1
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- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
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- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 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
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- QXJJQWWVWRCVQT-UHFFFAOYSA-K calcium;sodium;phosphate Chemical compound [Na+].[Ca+2].[O-]P([O-])([O-])=O QXJJQWWVWRCVQT-UHFFFAOYSA-K 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
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- 235000010418 carrageenan Nutrition 0.000 description 1
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- 235000019506 cigar Nutrition 0.000 description 1
- 229940001468 citrate Drugs 0.000 description 1
- 235000015165 citric acid Nutrition 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 238000004320 controlled atmosphere Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000008120 corn starch Substances 0.000 description 1
- 229910001647 dawsonite Inorganic materials 0.000 description 1
- SHFGJEQAOUMGJM-UHFFFAOYSA-N dialuminum dipotassium disodium dioxosilane iron(3+) oxocalcium oxomagnesium oxygen(2-) Chemical compound [O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[Na+].[Na+].[Al+3].[Al+3].[K+].[K+].[Fe+3].[Fe+3].O=[Mg].O=[Ca].O=[Si]=O SHFGJEQAOUMGJM-UHFFFAOYSA-N 0.000 description 1
- CVOQYKPWIVSMDC-UHFFFAOYSA-L dipotassium;butanedioate Chemical compound [K+].[K+].[O-]C(=O)CCC([O-])=O CVOQYKPWIVSMDC-UHFFFAOYSA-L 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000002657 fibrous material Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 229940050410 gluconate Drugs 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 239000001087 glyceryl triacetate Substances 0.000 description 1
- 235000013773 glyceryl triacetate Nutrition 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 229940093915 gynecological organic acid Drugs 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 239000011121 hardwood Substances 0.000 description 1
- 230000020169 heat generation Effects 0.000 description 1
- IPCSVZSSVZVIGE-UHFFFAOYSA-M hexadecanoate Chemical compound CCCCCCCCCCCCCCCC([O-])=O IPCSVZSSVZVIGE-UHFFFAOYSA-M 0.000 description 1
- 229940005740 hexametaphosphate Drugs 0.000 description 1
- 235000019534 high fructose corn syrup Nutrition 0.000 description 1
- 239000003906 humectant Substances 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 235000010977 hydroxypropyl cellulose Nutrition 0.000 description 1
- 239000001863 hydroxypropyl cellulose Substances 0.000 description 1
- 235000010979 hydroxypropyl methyl cellulose Nutrition 0.000 description 1
- 239000001866 hydroxypropyl methyl cellulose Substances 0.000 description 1
- 229920003088 hydroxypropyl methyl cellulose Polymers 0.000 description 1
- UFVKGYZPFZQRLF-UHFFFAOYSA-N hydroxypropyl methyl cellulose Chemical compound OC1C(O)C(OC)OC(CO)C1OC1C(O)C(O)C(OC2C(C(O)C(OC3C(C(O)C(O)C(CO)O3)O)C(CO)O2)O)C(CO)O1 UFVKGYZPFZQRLF-UHFFFAOYSA-N 0.000 description 1
- 239000010954 inorganic particle Substances 0.000 description 1
- 229910001867 inorganic solvent Inorganic materials 0.000 description 1
- 239000003049 inorganic solvent Substances 0.000 description 1
- 229940001447 lactate Drugs 0.000 description 1
- 229940040102 levulinic acid Drugs 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 1
- 239000000347 magnesium hydroxide Substances 0.000 description 1
- 229910001862 magnesium hydroxide Inorganic materials 0.000 description 1
- HCWCAKKEBCNQJP-UHFFFAOYSA-N magnesium orthosilicate Chemical compound [Mg+2].[Mg+2].[O-][Si]([O-])([O-])[O-] HCWCAKKEBCNQJP-UHFFFAOYSA-N 0.000 description 1
- 239000000391 magnesium silicate Substances 0.000 description 1
- 229910052919 magnesium silicate Inorganic materials 0.000 description 1
- 235000019792 magnesium silicate Nutrition 0.000 description 1
- 239000001630 malic acid Substances 0.000 description 1
- 235000011090 malic acid Nutrition 0.000 description 1
- 229910001437 manganese ion Inorganic materials 0.000 description 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical class C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 229940016286 microcrystalline cellulose Drugs 0.000 description 1
- 235000019813 microcrystalline cellulose Nutrition 0.000 description 1
- 239000008108 microcrystalline cellulose Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 229940049964 oleate Drugs 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 239000012766 organic filler Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 239000013618 particulate matter Substances 0.000 description 1
- 239000010451 perlite Substances 0.000 description 1
- 235000019362 perlite Nutrition 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 239000000244 polyoxyethylene sorbitan monooleate Substances 0.000 description 1
- 229920000053 polysorbate 80 Polymers 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229960003975 potassium Drugs 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 235000011056 potassium acetate Nutrition 0.000 description 1
- 229960004109 potassium acetate Drugs 0.000 description 1
- 235000010408 potassium alginate Nutrition 0.000 description 1
- 239000000737 potassium alginate Substances 0.000 description 1
- MZYRDLHIWXQJCQ-YZOKENDUSA-L potassium alginate Chemical compound [K+].[K+].O1[C@@H](C([O-])=O)[C@@H](OC)[C@H](O)[C@H](O)[C@@H]1O[C@@H]1[C@@H](C([O-])=O)O[C@@H](O)[C@@H](O)[C@H]1O MZYRDLHIWXQJCQ-YZOKENDUSA-L 0.000 description 1
- 239000001103 potassium chloride Substances 0.000 description 1
- 235000011164 potassium chloride Nutrition 0.000 description 1
- 239000001508 potassium citrate Substances 0.000 description 1
- 229960002635 potassium citrate Drugs 0.000 description 1
- QEEAPRPFLLJWCF-UHFFFAOYSA-K potassium citrate (anhydrous) Chemical compound [K+].[K+].[K+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O QEEAPRPFLLJWCF-UHFFFAOYSA-K 0.000 description 1
- 235000011082 potassium citrates Nutrition 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 238000005086 pumping Methods 0.000 description 1
- YGSDEFSMJLZEOE-UHFFFAOYSA-M salicylate Chemical compound OC1=CC=CC=C1C([O-])=O YGSDEFSMJLZEOE-UHFFFAOYSA-M 0.000 description 1
- 229960001860 salicylate Drugs 0.000 description 1
- 239000003352 sequestering agent Substances 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 235000010413 sodium alginate Nutrition 0.000 description 1
- 239000000661 sodium alginate Substances 0.000 description 1
- 229940005550 sodium alginate Drugs 0.000 description 1
- 229920001027 sodium carboxymethylcellulose Polymers 0.000 description 1
- 239000001509 sodium citrate Substances 0.000 description 1
- NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 1
- FQENQNTWSFEDLI-UHFFFAOYSA-J sodium diphosphate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OP([O-])([O-])=O FQENQNTWSFEDLI-UHFFFAOYSA-J 0.000 description 1
- MZSDGDXXBZSFTG-UHFFFAOYSA-M sodium;benzenesulfonate Chemical class [Na+].[O-]S(=O)(=O)C1=CC=CC=C1 MZSDGDXXBZSFTG-UHFFFAOYSA-M 0.000 description 1
- 239000011122 softwood Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 229940114926 stearate Drugs 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 229940086735 succinate Drugs 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 239000006188 syrup Substances 0.000 description 1
- 235000020357 syrup Nutrition 0.000 description 1
- 229940095064 tartrate Drugs 0.000 description 1
- 235000019818 tetrasodium diphosphate Nutrition 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 229960002622 triacetin Drugs 0.000 description 1
- 239000001069 triethyl citrate Substances 0.000 description 1
- VMYFZRTXGLUXMZ-UHFFFAOYSA-N triethyl citrate Natural products CCOC(=O)C(O)(C(=O)OCC)C(=O)OCC VMYFZRTXGLUXMZ-UHFFFAOYSA-N 0.000 description 1
- 235000013769 triethyl citrate Nutrition 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- 238000009423 ventilation Methods 0.000 description 1
- 239000010455 vermiculite Substances 0.000 description 1
- 235000019354 vermiculite Nutrition 0.000 description 1
- 229910052902 vermiculite Inorganic materials 0.000 description 1
- 230000004580 weight loss Effects 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 235000010493 xanthan gum Nutrition 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 229940082509 xanthan gum Drugs 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- UHVMMEOXYDMDKI-JKYCWFKZSA-L zinc;1-(5-cyanopyridin-2-yl)-3-[(1s,2s)-2-(6-fluoro-2-hydroxy-3-propanoylphenyl)cyclopropyl]urea;diacetate Chemical compound [Zn+2].CC([O-])=O.CC([O-])=O.CCC(=O)C1=CC=C(F)C([C@H]2[C@H](C2)NC(=O)NC=2N=CC(=CC=2)C#N)=C1O UHVMMEOXYDMDKI-JKYCWFKZSA-L 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A24—TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
- A24D—CIGARS; CIGARETTES; TOBACCO SMOKE FILTERS; MOUTHPIECES FOR CIGARS OR CIGARETTES; MANUFACTURE OF TOBACCO SMOKE FILTERS OR MOUTHPIECES
- A24D1/00—Cigars; Cigarettes
-
- 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
- A24B15/165—Chemical features of tobacco products or tobacco substitutes of tobacco substitutes comprising as heat source a carbon fuel or an oxidized or thermally degraded carbonaceous fuel, e.g. carbohydrates, cellulosic material
-
- A—HUMAN NECESSITIES
- A24—TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
- A24D—CIGARS; CIGARETTES; TOBACCO SMOKE FILTERS; MOUTHPIECES FOR CIGARS OR CIGARETTES; MANUFACTURE OF TOBACCO SMOKE FILTERS OR MOUTHPIECES
- A24D1/00—Cigars; Cigarettes
- A24D1/18—Selection of materials, other than tobacco, suitable for smoking
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Cigarettes, Filters, And Manufacturing Of Filters (AREA)
- Manufacture Of Tobacco Products (AREA)
- Paper (AREA)
Abstract
A combustible smokable filler material includes an agglomerated matrix of an inorganic component (e.g., particles of calcium carbonate) and an organic component (e.g., an alginate). The smokable filler material also includes a binding agent, and an aerosol forming material. Tobacco extracts and/or pieces of tobacco laminae can be incorporated into the smokable filler material, and/or the smokable filler material can be blended with tobacco cut filler. Cigarettes are provided by wrapping the smokable filler material in a paper wrapping material. A typical paper wrapping material has a porosity of less than about 5 CORESTA units.
Description
20265~9 ~ 1 RBP File No. 4109-07g Title: CIGARET~E AND ~MO~ART.~ FILLER MATl;~RTAT. TEIEREFOR
FIELD OF THE lNV~;N'l'lON
The present invention relates to cigarettes and other smoking articles, and in particular to cigarettes, which when smoked, yield relatively low levels of incomplete combustion products, generate low amounts of sidestream "tar" and odor, and sustain smolder during FTC
smoking conditions.
Popular smoking articles, such as cigarettes, have a lo substantially cylindrical rod shaped structure and include a roll or charge of smokable material, such as shredded tobacco material (e.g., in cut filler form), wrapped in a paper wrapper, thereby forming a so-called "smokable rod". Normally, a cigarette has a cylindrical filter element aligned in an end-to-end relationship with the smokable rod. Typically, a filter element includes cellulose acetate tow circumscribed by plug wrap, and is attached to the smokable rod using a circumscribing tipping material.
Typically, cigarettes are employed by the smoker by lighting one end thereof and burning the smokable rod.
As such, smoke normally is provided by burning smokable material, which typically is tobacco cut filler. The smoker then receives mainstream smoke (e.g., mainstream tobacco smoke) into his/her mouth by drawing on the Y-119A-R&D:1 2026~3!3 _ - 2 opposite end (e.g., the filter end) of the cigarette. As such, the smoker is provided with the pleasures of smoking (e.g., smoking taste, feel, satisfaction, and the like).
During the time that the cigarette is burning, sidestream smoke is generated. Sidestream smoke is smoke which directly enters the atmosphere from the lit end of the cigarette. Sidestream smoke diffuses into the atmosphere, and the characteristic visible nature and odor thereof may be perceived negatively by some individuals. The relative amount of visible sidestream smoke generated by a burning cigarette is related to the amount of sidestream "tar" generated by that burning cigarette. Typical commercially available cigarettes which burn tobacco cut filler, and have lengths of about 84 mm (e.g., having a smokable rod length of about 57 mm and a filter element length of about 27 mm), often yield about 25 to about 35 mg of sidestream "tar" per cigarette. See, Proctor et al, Analyst, Vol. 113, p.
1509 (1988), for an apparatus and technique for determining the sidestream "tar" of a cigarette.
Numerous cigarettes which reportedly yield relatively low levels of visible sidestream smoke have been proposed. See, for example, U.S. Patent Nos.
4,637,410 to Luke; 4,624,268 to Baker et al: 4,407,308 to Baker; 4,231,377 to Cline et al; 4,420,002 to Cline;
4,450,847 to Owens; 4,108,151 to Martin; 4,225,636 to Cline; 4,433,697 to Cline; 4,461,311 to Mathews et al;
and 4,561,454 to Guess.
Through the years, there have been proposed various methods for altering the composition of mainstream tobacco smoke. For example, many tobacco substitute materials have been proposed, and a substantial listing of such materials can be found in U.S. Patent No.
4,079,742 to Rainer et al. ln addition, tobacco Y-119A-R&D:2 -~ tR~ ks A- substitute smoking materials having the tradcna~ Cytrel and NSM were introduced in Europe during the 1970's.
Numerous references have proposed articles which generate flavored vapor and/or visible aerosol. Most of 5 such articles have employed a combustible fuel source to provide an aerosol and/or to heat an aerosol forming material. See, for example, the background art cited in U.S. Patent No. 4,714,082 to Banerjee et al.
Smoking articles which are capable of providing the lo pleasures associated with cigarette smoking, by heating but not necessarily burning tobacco, and without delivering considerable quantities of incomplete combustion products, are described in U.S. Patent Nos.
4,714,082 to Banerjee et al; 4,756,318 to Clearman et al;
and 4,793,365 to Sensabaugh, Jr. et al. Such smoking articles employ a combustible fuel element for heat generation; and aerosol forming substances positioned physically separate from, and in a heat exchange relationship with, the fuel element. During use, heat 20 generated by the fuel element acts to volatilize the aerosol forming substances, thereby providing an aerosol which resembles tobacco smoke. Such smoking articles yield extremely low levels of visible sidestream smoke as well as low levels of FTC "tar".
It would be desirable to provide a good tasting cigarette which provides good smoking satisfaction, provides relatively low mainstream gas phase yields, provides relatively low levels of incomplete combustion products, sustains smolder during FTC smoking conditions, and generates low levels of sidestream "tar" and hence low levels of visible sidestream smoke.
Y-119A-R&D:3 ~ ~ 4 ~ 2026533 SUMMARY OF THE INVENTION
The present invention relates to smoking articles incorporating tobacco in cut filler form and/or in a processed form. Preferred smoking articles have the form of a cigarette having two essential components: (i) a roll or charge of smokable material, and (ii) an outer wrapping material (e.g., a paper wrapper) circumscribing the roll of smokable material. Cigarettes of the present invention incorporate a smokable filler material lo (described in greater detail hereinafter) as at least a portion of the smokable material thereof.
The preferred wrapping material, which surrounds the roll of smokable material to thereby form a "smokable rod", is a low air permeability cigarette paper wrapper.
Highly preferred wrappers having a low air permeability or low porosity exhibit a porosity below about 5 CORESTA
units. A CORESTA unit is a measure of the linear air velocity which passes through a 1 cm2 area of wrapper at a constant pressure of 1 centibar. See CORESTA Publication ISO/TC 126/SC I N159E (1986).
One form of smokable material is a tobacco-containing smokable filler material. Such a smokable material of the present invention comprises an intimate mixture of (i) tobacco (e.g., shredded tobacco laminae, pieces of tobacco stems, milled tobacco laminae, tobacco fines, tobacco dust, or a tobacco extract or other form of processed tobacco), and (ii) an agglomerated matrix filler having, in intimate contact, an organic component and an inorganic component. Preferably, the agglomerated matrix filler is provided in particulate form. The organic component is an alginate or other organic material capable of providing an agglomerated matrix filler which is essentially insoluble in water at ambient conditions. Normally, the inorganic component is calcium Y-119A-R&D:4 2026~39 -carbonate. The smokable filler material includes a binding agent in intimate contact with the agglomerated matrix filler and tobacco. As such, the binding agent acts to maintain particles of the tobacco and agglomerated matrix filler together to form the smokable filler material. Such a tobacco-containing smokable filler material also can include certain flavoring agents (e.g., cocoa, licorice, organic acids, menthol, and the like) and/or aerosol forming materials (e.g., glycerin, propylene glycol, and the like) in intimate contact therewith. The tobacco-containing smokable filler material can be cast as a sheet from an aqueous slurry, provided as a sheet using a paper-making process, or provided in extruded form. Such a tobacco-containing smokable filler material can be employed individually as the sole smokable material of the cigarette, or that tobacco-containing smokable filler material can be physically mixed with (i.e., blended) or otherwise employed with other smokable materials, such as tobacco cut filler.
Another form of smokable filler material of the present invention comprises an intimate mixture of agglomerated matrix filler having, in intimate contact, an organic component and an inorganic component.
Preferably, the agglomerated matrix filler is provided in particulate form. The organic component is an alginate or other organic material capable of providing an agglomerated inorganic filler material which is essentially insoluble in water at ambient conditions.
Normally, the inorganic component is calcium carbonate.
The smokable filler material includes a binding agent in intimate contact with the agglomerated matrix filler. As such, the binding agent acts to maintain particles of agglomerated matrix filler together to form the smokable filler material. Such a smokable filler material also Y-119A-R&D:5 -6- ~6~39 can include certain flavoring agents and/or aerosol forming materials in intimate contact therewith. The smokable filler material can be cast as a sheet from an aqueous slurry, provided as a sheet using a paper-making process, or provided in extruded form. Such a smokable filler material can be physically mixed with or otherwise employed with tobacco-cont~i n ing smokable materials and/or tobacco cut filler.
Nore specifically, a smokable filler material for a cigarette according to the invention may have incorporated therein an intimate mixture of agglomerated matrix filler having an inorganic component, and tobacco. The agglomerated matrix filler may be in an agglomerated form having particles of inorganic filler component spaced within a continuous or semi-continuous phase of organic component prior to formation of the intimate mixture.
In another aspect, a smokable filler material for a cigarette may have incorporated therein agglomerated matrix filler having an inorganic filler component and organic component. The agglomerated matrix filler may be in an agglomerated form having particles of inorganic filler component spaced within a continuous or semi-continuous phase of organic component prior to formation of the smokable filler material.
According to a further aspect of the invention, a smokable filler material for a cigarette may have incorporated therein an intimate mixture of (i) agglomerated matrix filler having particles of inorganic component spaced within a continuous or semi-continuous phase of an organic binding component, the agglomerated matrix filler being essentially insoluble in water at ambient conditions, and (ii) tobacco; the agglomerated matrix filler being in an agglomerated form prior to formation of the intimate mixture.
-6a- 2026539 According to a still further aspect of the invention, a smokable filler material for a cigarette may have incorporated therein agglomerated matrix filler having particles of inorganic component spaced within a continuous or semi-continuous phase of an organic binding component, the agglomerated matrix filler being essentially insoluble in water at ambient conditions, and being in an agglomerated form prior to formation of the smokable filler material.
BRIEF DESCRIPTION OF THE DRAWINGS
Figures 1 through 4 are longitudinal sectional views of smoking articles of the present invention.
DETATT.~D DESCRIPTION OF THE PREFERRED EMBODIMENTS
A preferred embodiment of a cigarette and smokable filler material of the present invention is shown in Figure 1. The cigarette 10 includes a generally cylindrical rod 15. The rod includes a roll of smokable material 20 wrapped in at least one layer of circumscribing outer wrapping material 25 (e.g., paper). The rod 15 is hereinafter referred to as a "smokable rod". The ends of the smokable rod are open to exposed the smokable material which is to be burned. The smokable rod is used by lighting one end thereof, and aerosol (e.g., smoke) is provided as a result of the combustion of the burning smokable material. As such, the smokable rod burns from the lit end thereof towards the opposite end thereof.
The cigarette 10 also includes a filter element 30 positioned adjacent one end of the smokable rod 15 such that the filter element and smokable rod are axially aligned in an end-to-end relationship, preferably abutting one another. Filter element 30 has a generally cylindrical shape, and the diameter thereof is essentially equal to the diameter of the smokable rod.
The ends of the filter element are open to permit the passage of air and smoke therethrough. The preferred filter element has at least two filter segments. As shown in Figure 1, a first filter segment is positioned adjacent the smokable rod, and preferably includes a carbonaceous filter material 35 circumscribed by a wrapping material 37; while a second filter segment is positioned at the extreme mouthend of the cigarette, and preferably includes a filter material 40, such as a gathered non-woven polypropylene web or cellulose acetate tow, circumscribed by a wrapping material 45. The filter material 40 of the segment preferably is a material which provides an aesthetically pleasing, white appearance.
Each of the filter segments is manufactured using known filter rod making machinery. The two segments are combined using known plug tube combining techniques, and are held together using circumscribing wrap 50 so as to form the filter element.
The filter element 30 normally is attached to the smokable rod 15 by tipping material 55, which circumscribes both the entire length of the filter element and an adjacent region of the smokable rod. The inner surface of the tipping material 55 is fixedly secured to the outer surface of the plug wrap 50 and the outer surface of the wrapping material 25 of the smokable rod, using a suitable adhesive. The cigarette 10 can be manufactured using known cigarette making techniques and equipment. Optionally, a ventilated or air diluted cigarette is provided with an air dilution means such as a series of perforations 65 which extend through the tipping material 55, plug wrap 50 and wrapping material 37. Such ventilation can be provided to the cigarette Y-119A-R&D:7 using known techniques, such as laser perforation techniques.
Another preferred embodiment of a cigarette and smokable filler material of the present invention is shown in Figure 2. The cigarette 10 is generally similar to the cigarette described with reference to Figure 1, except that the smokable material has the form of a blend which is provided in a segmented fashion. At one end of the smokable rod 15 (i.e., at the end of the cigarette to lo be lit) is located a first segment 70 of smokable material. At the other end of the smokable rod 15 (i.e., at the end of the smokable rod adjacent the filter element) is located a second segment 75 of smokable material. Each segment is defined or identified in terms of its composition (i.e., the composition of each segment is different). The segments are aligned in an abutting, end-to-end relationship; however, there can be a certain amount of intermixing of smokable materials in the region where the two segments meet. The length which each segment of smokable material extends along the smokable rod can vary. However, the relative longitudinal length of the first segment relative to the second segment normally ranges from about 1:2 to about 2:1, with about 1:1 being preferred. Such smokable rods can be manufactured using apparatus described in U.S. Patent Nos. 4,009,722 to Wahle et al and 4,516,585 to Pinkham.
For preferred cigarettes of the type shown in Figure 2, the first segment 70 normally includes of tobacco in some type of smokable form. Such a form of tobacco includes tobacco cut filler (e.g., tobacco laminae, processed tobacco materials, volume expanded tobacco filler, reconstituted tobacco filler materials, and the like, and blends thereof), and blends thereof with other smokable materials. Examples of processed tobacco materials are deproteinated reconstituted tobacco Y-119A-R&D:8 materials described in U.S. Patent Nos. 4,887,618 to Bernasek et al and 4,941,484 to Clapp et al. Preferred cigarettes also have a second segment 75 which includes a smokable material or blend of smokable materials different in overall composition from the overall composition of the smokable material(s) of the first segment 70. The first segment 70 and/or the second segment 75 include at least one smokable filler material of the present invention.
Another preferred embodiment of a cigarette of the present invention is shown in Figure 3. The cigarette 10 is generally similar to the cigarette described with reference to Figures 1 and 2, except that the smokable material 20, which incorporates smokable filler material of the present invention is wrapped or contained in a processed tobacco sheet 80, or other inner wrapper material. The processed tobacco sheet 80 normally is a reconstituted tobacco sheet which is manufactured using a paper-making process, and a single layer of the sheet circumscribes the smokable material 20. The smokable material 20 wrapped in the processed tobacco sheet 80 is in turn wrapped in a single layer of circumscribing outer wrapping material 25 (e.g., cigarette paper).
Another preferred embodiment of a cigarette of the present invention is shown in Figure 4. The cigarette 10 is generally similar to the cigarette described with reference to Figures 1, 2 and 3, except that the filter element includes three segments. Segment 85, positioned between first filter material 35 and filter material 40, preferably is composed of a particulate matter such as Y-119A-R&D:9 activated carbon granules, magnesium silicate granules, silica gel particles, or the like.
The smokable material employed in the manufacture of the smokable rod can vary, and most preferably has the form of cut filler. As used herein, the term "cut filler" in referring to smokable materials is meant to include smokable materials which have a form suitable for use in the manufacture of smokable rods for cigarettes.
As such, cut filler can include smokable materials which are blended and are in a form ready for cigarette manufacture. Smokable materials normally are employed in the form of strands or shreds as is common in cigarette manufacture. For example, cut filler can be employed in the form of strands or shreds cut from sheet-like or "strip" materials. Such strip materials are cut into widths ranging from about 1/5 inch to about 1/60 inch, preferably from about 1/25 inch to about 1/35 inch.
Generally, the resulting strands or shreds have lengths which range from about 0.25 inch to about 3 inches. Cut filler also can have an extruded form (e.g., extruded strands) or other physically processed form.
The smokable rods of cigarettes of the present invention include smokable filler material of the present invention. The smokable filler material can be employed in cut filler form.
One preferred type of smokable filler material of the present invention comprises an agglomerated matrix filler including an agglomerated matrix of an organic component and an inorganic component in intimate contact.
The agglomerated matrix filler is in turn intimately mixed with a binding agent to provide the smokable filler material. Such a smokable filler material most preferably includes as part of the ultimate mixture, at least one aerosol forming material and/or at least one flavoring agent. If desired, other agents, which have Y-119A-R&D:10 the ability to alter the composition of the aerosol generated by the smokable filler material, can be incorporated into that smokable filler material. The agglomerated matrix filler normally includes about 2 to about 99, preferably about 5 to about 20 weight parts inorganic component for each weight part of organic component. Such a smokable filler material normally includes about 60 to about 90, preferably about 65 to about 85 weight percent agglomerated matrix filler; up to about 20, preferably about 2 to about 10 weight percent binding agent; up to about 20, preferably about 3 to about 15 weight percent aerosol forming material; and sufficient amounts of flavoring agent to provide the desired flavor characteristics. If desired, a carbonaceous material (e.g., pyrolyzed alpha cellulose) can be incorporated into the smokable filler material, usually in amounts of up to about 10, and sometimes up to about 30 weight percent, based on the total dry weight of the smokable filler material. However, such further carbonaceous material is not a necessary component of the smokable filler material, and the smokable filler material can be absent of such carbonaceous material.
Such a smokable filler material is combustible and can be employed with (e.g., blended with) another smokable material (e.g., tobacco cut filler) in order to provide a cigarette of the present invention.
One preferred type of tobacco-containing smokable filler material of the present invention comprises an agglomerated matrix filler including an agglomerated matrix of an organic component and an inorganic component, which agglomerated matrix filler is in turn intimately mixed with some form of tobacco and binding agent, to provide smokable filler material. Such a tobacco-containing smokable filler material preferably includes as part of the ultimate mixture, at least one Y-119A-R&D:ll - 12 _ 2026539 aerosol forming material and/or at least one flavoring agent. If desired, other agents, which have the ability to alter the composition of the aerosol generated by the smokable filler material, can be incorporated into that smokable filler material. The agglomerated matrix filler normally includes about 2 to about 99, preferably about 5 to about 20 weight parts inorganic component for each weight part of organic component. Such a tobacco-containing smokable filler material normally includes up to about 75, typically up to about 50 weight percent of some form of tobacco; up to about 80, preferably about 20 to about 60 weight percent agglomerated matrix filler; up to about 20, preferably about 2 to about 10 weight percent binding agent; up to about 20, preferably about 3 to about 15 weight percent aerosol forming material; and sufficient amounts of flavoring agent to provide desired flavor characteristics. If desired, a carbonaceous material (e.g., pyrolyzed alpha cellulose~ can be incorporated into the smokable filler material, usually in amounts of up to about 10, and sometimes up to about 30 weight percent, based on the total dry weight of the smokable filler material. However, such further carbonaceous material is not a necessary component of the smokable filler material, and the smokable filler material can be absent of such carbonaceous material. Such a smokable filler material is combustible and can be employed individually as the sole smokable material of a cigarette of the present invention.
Another preferred type of smokable filler material of the present invention comprises an agglomerated matrix filler of an organic component and an inorganic component. The agglomerated matrix filler is intimately mixed with a binding agent and at least one aerosol forming material to provide the smokable filler material.
Y-119A-R~D:12 Such a smokable filler material most preferably includes as part of the ultimate mixture, at least one flavoring agent and some form of tobacco. The agglomerated matrix filler normally includes about 2 to about 99 weight parts inorganic component for each part of organic component.
Such a smokable filler material normally includes up to about 20, preferably about 3 to about 15 weight percent binding agent; greater than about 20, preferably about 25 to about 80, more preferably about 30 to about 50 weight percent aerosol forming material; and less than about 80, preferably about 30 to about 70 weight percent filler component including the previously described agglomerated matrix filler. In particular, the filler component can include (i) all of the previously described agglomerated matrix filler, or (ii) a blend of the previously described agglomerated matrix filler with an inorganic filler material (e.g., precipitated calcium carbonate) and/or an organic filler material (e.g., tobacco).
Amounts of flavoring agent sufficient to provide the desired flavor characteristics to the smokable filler material can be incorporated into the smokable material.
If desired, a carbonaceous material (e.g., pyrolyzed alpha cellulose) can be incorporated into the smokable material, usually in amounts of up to about 10, and sometimes up to about 30 weight percent, based on the total dry weight of the smokable material. However, such further carbonaceous material is not a necessary component of the smokable material, and the smokable material can be absent of such carbonaceous material.
The smokable filler material is combustible and can be blended with other smokable materials.
The tobacco-containing smokable filler materials of the present invention have some form of tobacco incorporated therein during its manufacture. The tobacco which is employed to provide such a tobacco-containing Y-119A-R&D:13 `~ - 14 - 202653~
smokable filler material can have a variety of forms, including tobacco extracts, tobacco fines or dust, shredded or comminuted tobacco laminae, tobacco stems, volume expanded tobacco filler and other forms of processed tobacco, and the like, and combinations thereof. Tobacco extracts are processed forms of tobacco and are provided by extracting a tobacco material using a solvent such as water, carbon dioxide, a hydrocarbon, or a halocarbon, as well as various other organic and inorganic solvents. Tobacco extracts can include spray dried extracts; freeze dried extracts; heat treated extracts; tobacco essences, such as those essences described in European Patent Publication No. 0326370 published August 2, 1989; and aroma oils and extracts described in U.S. Patent No. 4,506,682 to Mueller and Canadian Patent Application No. 596,617 filed April 13, 1989.
The smokable filler materials of the present invention incorporate a binding agent. Examples of suitable binding agents include hydroxypropylcellulose such as Klucel H from Aqualon Co.; hydroxypropyl-methylcellulose such as Methocel K4MS from The Dow Chemical Co.; hydroxyethylcellulose such as Natrosol 250 MRCS from Aqualon Co.; microcrystalline cellulose such as Avicel from FMC; methylcellulose such as Methocel A4M
from The Dow Chemical Co.; and sodium carboxymethyl-cellulose such as CMC 7HF and CMC 7H4F from Hercules Inc.
Especially preferred binding agents include the alginates, such as ammonium alginate, sodium alginate, propylene glycol alginate and potassium alginate. The alginates, and particularly the high viscosity alginates, can be employed in conjunction with controlled levels of free calcium ions. Other binding agents include starches Y-119A-R&D:14 -- 15 - 2026~39 (e.g., corn starch), carrageenan, guar gum, locust bean gum, pectins and xanthan gum. Combinations or blends of binding agents (e.g., a mixture of guar gum and locust bean gum) can be employed.
The smokable filler materials of the present invention can have at least one aerosol forming material and/or at least one flavoring agent incorporated therein.
The preferred aerosol forming materials include polyols (e.g, glycerin, propylene glycol or triethylene glycol), and any other materials which yield a visible aerosol, or combinations thereof. The aerosol forming material can be provided as a portion of the binding agent (e.g., when the binding agent is propylene glycol alginate).
Combinations of aerosol forming materials can be employed. The flavoring agents can vary, and include menthol, vanillin, citric acid, malic acid, cocoa, licorice, and the like, as well as combinations thereof.
See, Leffingwell et al, Tobacco Flavoring for Smoking Products (1972).
It is sometimes desirable to incorporate a caramelizing material into the smokable filler materials of the present invention. Caramelizing materials can act to improve (i) the integrity of the ash and fire cone of the cigarette, (ii) the appearance of the smokable filler material, and (iii) the flavor characteristics of the mainstream smoke of the cigarette. The caramelizing material can be incorporated into the smokable filler material during the preparation of that material and/or applied to the surface of that material (e.g., as a powder) after the manufacture thereof. Normally, the amount of caramelizing material which is employed to treat a particular smokable filler material is such that the resulting material which incorporates the caramelizing material includes up to about 20 weight parts of caramelizing material and greater than about 80 Y-119A-R&D:15 weight parts of the smokable material which is treated.
Examples of suitable caramelizing materials include sugars, such as glucose, fructose and sucrose; and compositions such as Carob Powder Code 1739 from M. F.
Neal, Inc.
The smokable filler materials of the present invention can be surface treated with certain substances.
For example, the smokable filler materials can have powdered substances applied to the surface thereof.
Exemplary substances include cocoa powder, licorice powder, powdered inorganic materials (e.g., potassium carbonate or iron oxide), tobacco dust, finely divided tobacco laminae, or the like, or blends thereof. The surface treatment of the smokable filler materials can provide to those materials improved color and appearance, improved as characteristics, and improved flavor characteristics.
The agglomerated matrix filler has an inorganic component and an organic component. For example, calcium carbonate agglomerated using an alginate has an inorganic component and an organic component. Other inorganic components include calcium sulfate, magnesium oxide and magnesium carbonate. Ammonium alginate is an especially preferred alginate. Such an agglomerated matrix filler can be provided by preparing an aqueous slurry of calcium carbonate particles and hydrated alginate, and drying the slurry to form an agglomerated matrix of calcium carbonate (i.e., a matrix of a plurality of calcium carbonate particles spaced within a continuous or semi-continuous phase of alginate). If desired, the slurrycan be volume expanded by incorporating a foaming agent therein. Examples of suitable foaming agents include linear sodium benzene sulfonates, linear alkyl sulfates and linear alkyl ethoxy sulfates. Preferably, a high solids content aqueous slurry of calcium carbonate and Y-119A-R&D:16 alginate is spray dried to provide agglomerated particles (e.g., normally spherical particles) of calcium carbonate particles and alginate. Alternatively, the slurry can be dried by the application of heat to provide a solid mass of agglomerated calcium carbonate and alginate, and the solid mass can be ground to yield particles of the desired size. Preferably, the amount of calcium carbonate relative to alginate ranges from about 99:1 to about 2:1, preferably about 20:1 to about 5:1, on a dry lo weight basis. Typically, the particles of calcium carbonate agglomerated using alginate are essentially insoluble in water under ambient conditions. In particular, the essentially insoluble character of the alginate in the agglomerated matrix filler tends to limit to a great degree any propensity of the agglomerated matrix filler to lose its agglomerated character when contacted with water under ambient conditions. The agglomerated matrix filler is rendered insoluble due to the interaction of the alginate with calcium ions of the calcium carbonate. If desired, the agglomerated matrix filler can be treated with a dilute solution of acid to decompose a portion of the calcium carbonate and the resulting calcium ions can act to render insoluble the alginate component of the agglomerated matrix filler.
The agglomerated matrix filler having an inorganic component and an organic component can incorporate a variety of other organic components. For example, the organic component can be pectin, which has a tendency to become essentially water insoluble upon interaction with calcium ions. Alternatively, agglomerated matrix filler having a polysaccharide organic component can be treated with divalent ions (e.g., calcium, barium, cobalt, iron or manganese ions) or trivalent ions (e.g., iron or aluminum ions) to render the polysaccharide essentially water insoluble. As yet another example, a slurry of Y-119A-R&D:17 - 202653~
polysaccharide material (e.g., ethylcellulose) and inorganic component particles can be provided in a non-aqueous solvent (e.g., alcohol) and dried, resulting in the formation of an agglomerated matrix filler which is essentially water insoluble.
Other inorganic materials can be incorporated as fillers in the smokable filler materials of the present invention. Such inorganic materials often have a fibrous, flake, crystalline, amorphous, hollow or particulate form. Examples of inorganic filler materials include calcium carbonate, calcium sulfate particles, magnesium oxide, magnesium hydroxide, perlite, synthetic mica, vermiculite, clays, thermally stable carbon fibers, zinc oxide, dawsonite, low density hollow spheres of calcium carbonate, glass spheres, glass bubbles, thermally stable carbon microspheres, calcium sulfate fibers, hollow ceramic microspheres, alumina, calcium carbonate particles agglomerated using a carbonaceous component, low density processed calcium carbonate, and the like.
The agglomerated matrix filler has the form of an agglomerated matrix of an inorganic component and a carbonaceous component. The inorganic component thereof can include particles of calcium carbonate, calcium sulfate, magnesium oxide, magnesium carbonate, and the like. A particularly preferred agglomerated matrix filler is agglomerated calcium carbonate, and most preferably, agglomerated precipitated calcium carbonate.
Such an agglomerated matrix filler is prepared by providing an aqueous slurry of calcium carbonate particles and a binding material, and drying the slurry to form an agglomerated matrix of calcium carbonate (i.e., a matrix of a plurality of calcium carbonate particles spaced within a continuous or semi-continuous phase of binding material). Calcium carbonate particles Y-119A-R&D:18 which are employed to provide the agglomerated matrix typically exhibit a surface area of less than about 20 m2/g, frequently less than about 10 m2/g, and sometimes less than about 1 m2/g, as determined using the Brunauer, Emmett and Teller (BET) method described in J. Am. Chem.
Soc., Vol. 60, p. 309 (1938). Typical binding materials are organic materials, such as cellulosic derivatives (e.g., sodium carboxymethylcellulose), and preferably are sugar containing materials, such as molasses, high fructose corn syrup, or Carob Powder Code 1739 from M. F.
Neal, Inc. Other organic materials, such as pectins, alginates and the other previously described organic materials, also can be employed.
Preferably, a high solids content aqueous slurry (e.g, about 40 to about 55 weight percent solids content slurry) of calcium carbonate and binding material is spray dried to provide agglomerated particles (e.g., normally spherical particles) of calcium carbonate particles and binding material. Alternatively, the slurry can be dried by the application of heat to provide a solid mass of agglomerated calcium carbonate and binding material, and the solid mass can be ground to yield particles of the desired size. Preferably, the amount of calcium carbonate relative to binding material ranges from about 20:1 to about 2:1, more preferably about 15:1 to about 4:1, on a dry weight basis.
Normally, the inorganic particles agglomerated using saccharide and polysaccharide materials tend to lose their agglomerated character when contacted with water under ambient conditions, as a result of the propensity of the saccharide and polysaccharide materials to be soluble in water.
The agglomerated matrix of inorganic component and organic binding material is subjected to heat treatment.
As such, volatile components from the organic binding Y-119A-R&D:19 ~ - 20 - 202653~
material are expelled, and the organic binding material is calcined to form an essentially water insoluble, clean burning carbonaceous component. Normally, the heat treatment of the agglomerated matrix filler is provided under controlled atmosphere, in order to minimize or prevent oxidation of the binding material. Preferably, the heat treatment provides a binding material which is in the form of a carbonaceous material, and in turn, provides a means for agglomerating the particles of inorganic component into a matrix form. In particular, the particles of agglomerated calcium carbonate and binding material can be heat-treated (e.g., to a temperature of up to about 625C, and usually up to about 600C) using an oven, a fluidized bed, rotary calciner, belt calciner, or the like. For example, particles of spray dried calcium carbonate particles agglomerated using molasses can be heated in a fluidized bed having gaseous nitrogen flowing therethrough, heated at temperatures sufficient to heat the particles to about 300C to about 625C, and collected. The agglomerated matrix of inorganic component and organic binding material can be subjected to heat treatment sufficient to calcine the organic binding material by subjecting the agglomerated matrix to very high temperatures (e.g., up to about 900C) for a short time period and under conditions sufficient to avoid decomposition of the inorganic component (e.g., when the inorganic component is calcium carbonate). However, if the inorganic component is calcium carbonate, and the calcium carbonate undergoes some decomposition during the calcining step, the agglomerated material can be re-carbonated by (i) exposing that material to carbon dioxide atmosphere, or Y-119A-R&D:20 ~026539 (ii) dispersing that material in water and bubbling carbon dioxide into the dispersion.
After the calcining process, the agglomerated calcium carbonate particles normally have a calcium carbonate content of greater than about 80, frequently greater than about 90 weight percent and a carbon content of greater than about 3 weight percent. Normally, the resulting agglomerated particles are screened to sizes of about -50/+325 US Mesh, and often about -80/+200 U.S.
Mesh. Preferred agglomerated calcium carbonate particles which have been calcined are essentially insoluble in water, are spherical in shape, are free flowing, and exhibit a bulk density of about 0.1 g/cm3 to about 1.1 g/cm3, frequently about 0.3 g/cm3 to about 1 g/cm3~, using mercury intrusion techniques. As such, calcined agglomerated calcium carbonate particles provide an inorganic material having a bulk density less than about 2 g/cm3, and preferably less than about 1 g/cm3, which includes an inorganic component having a bulk density greater than about 2.5 g/cm3. Normally, such calcined agglomerated calcium carbonate particles exhibit a surface area of less than about 30 m2/g, and often about 10 m2/g to about 25 m2/g, as determined using the BET
method.
If desired, the bulk density of the calcined agglomerated inorganic filler can be lowered by digesting away part of the inorganic component with an acidulant.
For example, calcined agglomerated can be dispersed in water, and an aqueous hydrochloric acid solution can be added to the resulting slurry which is agitated. The acid reacts with the calcium carbonate, and essentially does not react with the carbonaceous component. Thus, the carbonaceous component acts to hold together the remaining calcium carbonate, while a portion of the Y-119A-R&D:21 calcium carbonate reacts to produce carbon dioxide gas and water soluble calcium chloride.
Another type of inorganic material which can be incorporated into smokable filler materials of the S present invention is a low density inorganic filler.
Such a filler is provided by providing particles of a calcium salt, decomposing the anion of the salt and contacting the particles with carbon dioxide. Examples of suitable salts include calcium propionate, succinate, tartrate, stearate, salicylate, palmitate, oleate, lactate, gluconate, citrate, ascorbate, acetylsalicylate and benzoate. Other suitable salts include calcium salts of saccharides and polysaccharides. Such salts are subjected to conditions sufficient to decompose the anion thereof, which usually involves subjecting the salt to heat treatment under carbon dioxide atmosphere.
One method for providing a low density inorganic filler involves heating calcium lactate particles screened to -80/+170 US Mesh at about 600C for about 8 hours under a steady 228 ml/min. flow of carbon dioxide gas, so as to provide a material which has undergone about a 65 percent weight loss. About 20 weight parts of the material is charged into about 80 weight parts water and the resulting slurry is contacted with sufficient hydrochloric acid solution to lower the pH thereof to about 6.8. The material then is removed from the water, washed with water, dried, and screened to a particle size of -80/+170 US Mesh. Such material is greater than about 95 weight percent calcium carbonate, and exhibits a bulk density of about 0.4 g/cm3, as determined using mercury intrusion techniques.
Typically, the smokable filler materials of the present invention are provided by forming an aqueous slurry of binding agent and the other components of that smokable filler material, casting the slurry as a sheet, Y-119A-R&D:22 _ - 23 - 2026539 and drying the cast material to form a relatively dry, workable sheet. Techniques and equipment for casting a slurry as a sheet will be apparent to the skilled artisan. Other materials, such as calcium acetate, potassium carbonate, pH control agents, urea, amino acids, potassium chloride and/or calcium hydroxide, can be incorporated into the slurry. Sequestering agents (e.g., diammonium hydrogen orthophosphate, sodium citrate, potassium hexametaphosphate or tetrasodium pyrophosphate) can be incorporated into the slurry in amounts sufficient to control the free calcium ion concentration of the slurry. The cast material can be dried at ambient temperatures or at elevated temperatures. Further, an aqueous solution of calcium salts can be applied to the cast slurry. The resulting dried sheet can be cut or broken into "strip" form, and later can be cut or shredded into cut filler form.
The smokable filler materials of the present invention can be provided using a paper-making process. In particular, an aqueous slurry of a cellulosic material (e.g., softwood pulp, hardwood pulp, flax fibers and/or shredded tobacco stems) and the previously described filler can be cast as a mat on a fibrous belt or wire screen, and dried to the desired moisture level.
Normally, a slurry, dispersion or solution of flavoring agents, tobacco extracts, tobacco parts, aerosol forming materials, and the like, can be applied to the mat (e.g., as a spray), and the resulting mat can be dried further to form a sheet. The resulting dried sheet can be cut or broken in "strip" form, and later can be cut or shredded into cut filler form. Techniques and equipment for making a paper-type sheet will be apparent to the skilled artisan.
The smokable filler materials of the present invention can be extruded into the desired shape using Y-119A-R&D:23 suitable extrusion techniques. See, for example, the types of processes described in U.S. Patent No.4,880,018 to Graves, Jr. et al. Alternatively, an aqueous slurry of the components of the smokable and an alginate binding agent can be extruded into an aqueous solution of calcium ions (e.g., an aqueous solution of calcium chloride), collected and dried. If desired, extruded smokable filler materials can be physically processed (e.g., subjected to treatment using rollers, etc.) and formed into the desired shape.
The smokable rods of cigarettes of the present invention often include a physical mixture or blend of smokable materials. The blend can include two or more smokable filler materials of the present invention, or a physical mixture of at least one smokable filler material of the present invention with at least one other smokable material. Certain preferred cigarettes often include within such a blend, a sufficient amount of at least one of the smokable filler materials of the present invention such that the smokable material within each cigarette comprises at least about 1 percent of the carbonaceous material, based on the total weight of the blend. In particular, cigarettes having such types of smokable filler materials and having low porosity paper outer wrappers (e.g., having outer wrappers having less than about 5 CORESTA units) have the propensity to sustain smolder (e.g., not self-extinguish), when smoked under FTC smoking conditions. FTC smoking conditions consist of 35 ml puffs of 2 second duration, taken every 60 seconds.
The smokable filler materials of the present invention can be blended with tobacco cut filler. The type of tobacco can vary, and can include flue-cured, Burley, Maryland and Oriental tobaccos, as well as the Y-119A-R&D:24 2026~39 rare and specialty tobaccos, and blends thereof. Such tobacco cut filler can be provided in the form of tobacco laminae; volume expanded or puffed tobacco laminae;
processed tobacco stems such as cut-rolled or cut-puffed stems; reconstituted tobacco materials, such as (i) deproteinated tobacco materials described in U.S. Patent Nos. 4,887,618 to Bernasek et al and 4,941,484 to Clapp et al, (ii) a phosphate-containing reconstituted tobacco material described in U.S. Patent Nos. 3,353,541 and 3,420,241 to Hind et al, and 3,386,449 to Hind, (iii) a reconstituted tobacco material described in Tobacco Encyclopedia, edit. by Voges, p. 389, TJI (1984), or blends thereof.
Smokable materials can be cased and top dressed as is conventional during various stages of cigarette manufacture. For example, flavoring agents can be applied to the smokable material as is commonly performed - when cigarette cut filler is processed. Suitable flavoring agents include vanillin, cocoa, licorice, menthol, and the like. Flavor modifying agents can be applied to the smokable material. A flavor modifying agent in the form of levulinic acid can be applied to the smokable filler material (e.g., in amounts ranging from about 0.01 to about 2 percent, normally from about 0.1 to about 1 percent, preferably about 0.2 to about 0.6 percent, based on the dry weight of the smokable material). Another flavor modifying agent in the form of potassium carbonate can be applied to the smokable material (e.g., in amounts of less than about 5 percent, Y-119A-R&D:25 - 26 - 2026~39 normally about 2 to about 3 percent, based on the dry weight of the smokable material). Aerosol forming materials and humectants, such as glycerin and propylene glycol, can be applied to the smokable material. Such components conveniently are applied to the smokable material as casing and top dressing components.
The preferred wrapping material which provides the smokable rod is a cigarette wrapping material having a low air permeability value. Such a wrapping material normally has an air permeability of less than about 5 CORESTA units, often less than about 3 CORESTA units, and frequently less than about 1 CORESTA unit. Typical wrapping materials are cigarette paper wrappers.
Suitable wrapping materials are cigarette paper wrappers available as DD-71-1, DD-71-6, MTR-1021, P-2831-60-2, P-2831-60-3, P-2831-60-4, P-2831-60-5, P-2674-110, P-2831-60-1 and DD-100-2 from Kimberly-Clark Corp.
Suitable low porosity cigarette paper wrappers are commercially available, and can have various levels of burn chemicals, fluxing agents, etc., incorporated therein. Particularly preferred are cigarette paper wrappers which include an amount of a polymeric film forming agent sufficient to provide a paper having the desirably low air permeability value. For example, a sufficient amount of a solution of a polymeric (e.g., carboxymethyl cellulose or ethylcellulose) film forming agent can be applied to a paper wrapper. The selection of the polymeric film forming agent will be apparent to the skilled artisan.
The optional polymeric film forming agent can be applied to the paper wrapper during the manufacture of the paper, or applied as a print or paint after manufacture of the paper is complete. Typically, the film forming agent is applied to the paper as a dilute solution (e.g., at a concentration of about 0.2 to about Y-119A-R&D:26 ~ - 27 - 2026539 5 weight percent relative to the solvent) for ease of processing. The amount of film forming agent applied to the paper wrapper depends upon factors such as the permeability of the paper and the film forming capabilities of the film forming agent. Typically, the amount of film forming agents employed ranges from about 1 to about 10 percent, based on the dry weight of the paper. For example, a 5 weight percent solution of ethylcellulose in ethanol or sodium carboxymethyl-cellulose in water can be applied to cigarette paperusing a size press, and the paper can be dried to provide a non-wetting, moisture resistant paper wrapper having a porosity of less than about 1 CORESTA unit, preferably less than about 0.5 CORESTA unit.
The smokable rods and the resulting cigarettes can be manufactured in any known configuration using known cigarette making techniques and equipment. Smokable rods often include smokable material wrapped in a single layer of wrapping material, although a double layer of two types of wrapping materials can be employed.
Cigarettes having smokable rods which are double wrapped with two layers of wrapping material preferably include one of the previously described low porosity paper wrappers as the outer wrappers. The inner wrapper can vary, but typically is a tobacco-containing wrapping material. Exemplary inner wrappers are paper wrappers which include about 3 parts Java tobacco stem parts and about 1 part wood pulp, and are available from Kimberly-Clark Corp. as P-2249-115 and P-2831-23-3.
Other suitable inner wrapping materials include tobacco parts and carbonaceous materials, and are available from Kimberly-Clark Corp. as P-2540-94-A, P-2540-94-C and Y-119A-R&D:27 - 2026~39 P-2540-94-D. The inner wrapping materials (i) can include burn chemicals (e.g., potassium citrate, potassium acetate or potassium succinate), and/or (ii) act as a substrate for flavors (e.g., menthol or vanillin) or flavor precursors (e.g., vanillin glucoside or ethylvanillin glucoside).
Typically, the smokable rod has a length which ranges from about 30 mm to about 70 mm, preferably about 35 to about 60 mm; and a circumference of about 17 mm to about 27 mm, preferably about 22 mm to about 25 mm.
Short smokable rods (i.e., having lengths from about 30 to about 50 mm) can be employed, particularly when smokable materials having a relatively high packing density are employed.
The packing density of the smokable material contained within the outer wrapping material can vary.
Typical packing densities for smokable rods of cigarettes of the present invention range from about 150 to about 400 mg/cm3. Normally, packing densities of such smokable rods range from about 200 to about 380 mg/cm3, frequently about 250 to about 360 mg/cm3, particularly when relatively short (i.e., less than 50 mm long) smokable rods are employed.
The cigarettes of the present invention preferably include a filter element, and most preferably a filter element having more than one segment. For example, a preferred filter element has two or more filter segments.
Typically, the segments of the preferred filter elements each have lengths which ranges from about 10 mm to about 30 mm; and circumferences of about 17 mm to about 27 mm, preferably about 22 mm to about 25 mm. The plug wrap which circumscribes the filter material of each filter segment typically is a conventional paper plug wrap, and can be either air permeable or essentially air impermeable.
Y-119A-R&D:28 - 29 - 2026~39 Preferred filter materials of one of the filter ,egments include carbonaceous materials (e.g., activated carbon particles, charcoal particles, or carbon paper).
An example of a particularly preferred filter material is provided by gathering a tobacco/carbon paper available as P-144-BAC from Kimberly-Clark Corp. Such filter materials reduce the levels of certain gas phase components from the mainstream smoke which passes to the mouth of the smoker. As such, preferred filter materials of that segment act to reduce the levels of any smoke components which may provide an off-taste or other undesirable characteristics to the mainstream smoke.
Preferred filter materials of another of the filter segments normally include fibrous materials. An example of a suitable filter material is a gathered nonwoven polypropylene web. A particularly preferred nonwoven polypropylene sheet-like web is available as PP-100-F
from Kimberly-Clark Corp. Another example of a suitable filter material is a cellulose acetate tow. Particularly preferred cellulose acetate tow items include (i) 8 denier per filament/40,000 total denier, and (ii) 8 denier per filament/15,000 total denier, (iii) 8 denier per filament/25,000 total denier, and (iv) 8 denier per filament/30,000 total denier. Plasticizers, such as triacetin, propylene glycol or triethyl citrate, can be combined with the filler materials.
Another filter segment can have a filter material in the form of a gathered web of nonwoven thermoplastic (i.e., hydrophobic) fibers in intimate contact with a water soluble tobacco extract so as to provide an extract-containing filter material. A highly preferred web is a nonwoven web of polypropylene fibers available as PP 200 SD from Kimberly-Clark Corp. Such segments can Y-119A-R&D:29 _ - 30 - 2026539 provide enhanced flavor characteristics to the mainstream smoke which passes therethrough.
Yet another filter segment can include a tobacco paper material as the filter material. For example, a filter material can have the form of a gathered web of tobacco paper available as P-144-B from Kimberly-Clark Corp.
The filter element segments suitable for use in this invention can be manufactured using known cigarette filter making techniques. Filter elements can be manufactured from cellulose acetate tow using known techniques. Filter elements can be manufactured from carbon paper, tobacco paper and a sheet-like nonwoven polypropylene web using filter making techniques described in U.S. Patent No. 4,807,809 to Pryor et al.
Alternatively, particles of charcoal or activated carbon can be incorporated into the filter element using a so-called "triple filter" configuration by positioning the particles between two segments of suitable filter materials.
The filter elements can have low, moderate or high filtration efficiencies. Preferred filter elements have minimal mainstream aerosol (i.e., smoke) removal efficiencies while maintaining the desirable draw characteristics of the cigarette. Such minimal smoke removal efficiencies are provided by "low efficiency filter elements. Low efficiency filter elements have a minimal ability to remove mainstream smoke particulates.
See, Keith in Schemeltz's The Chemistry of Tobacco and Tobacco Smoke, p. 157 (1972). Generally, low efficiency filter elements provide less than about 40 weight percent mainstream smoke particulate removal efficiency.
Y-119A-R&D:30 `~ 2026539 Tipping material circumscribes the filter element and an adjacent region of the smokable rod such that the tipping material extends about 3 mm to about 6 mm along the length of the smokable rod. Typically, the tipping material is a conventional paper tipping material.
Tipping materials of varying porosities can be employed.
For example, the tipping material can be essentially air impermeable, air permeable, or treated (e.g., by mechanical or laser perforation techniques) so as to have a region of perforations, openings or vents thereby providing a means for providing air dilution to the cigarette. The total surface area of the perforations and the positioning of the perforations along the periphery of the cigarette can be varied in order to control the performance characteristics of the cigarette.
For air diluted or ventilated cigarettes of the present invention, the amount of air dilution can vary.
Typically, the amount of air dilution for an air-diluted cigarette is greater than about 25 percent, and frequently greater than about 40 percent. The upper limit for air dilution for a cigarette typically is less than about 75 percent, more frequently less than about 65 percent. As used herein, the term "air dilution" is the ratio (expressed as a percentage) of the volume of air drawn through the air dilution means to the total volume of air and aerosol (i.e., smoke) drawn through the cigarette and exiting the extreme mouthend portion of the cigarette. See, Selke et al, Beitr. Zur Tabak. In., Vol.
FIELD OF THE lNV~;N'l'lON
The present invention relates to cigarettes and other smoking articles, and in particular to cigarettes, which when smoked, yield relatively low levels of incomplete combustion products, generate low amounts of sidestream "tar" and odor, and sustain smolder during FTC
smoking conditions.
Popular smoking articles, such as cigarettes, have a lo substantially cylindrical rod shaped structure and include a roll or charge of smokable material, such as shredded tobacco material (e.g., in cut filler form), wrapped in a paper wrapper, thereby forming a so-called "smokable rod". Normally, a cigarette has a cylindrical filter element aligned in an end-to-end relationship with the smokable rod. Typically, a filter element includes cellulose acetate tow circumscribed by plug wrap, and is attached to the smokable rod using a circumscribing tipping material.
Typically, cigarettes are employed by the smoker by lighting one end thereof and burning the smokable rod.
As such, smoke normally is provided by burning smokable material, which typically is tobacco cut filler. The smoker then receives mainstream smoke (e.g., mainstream tobacco smoke) into his/her mouth by drawing on the Y-119A-R&D:1 2026~3!3 _ - 2 opposite end (e.g., the filter end) of the cigarette. As such, the smoker is provided with the pleasures of smoking (e.g., smoking taste, feel, satisfaction, and the like).
During the time that the cigarette is burning, sidestream smoke is generated. Sidestream smoke is smoke which directly enters the atmosphere from the lit end of the cigarette. Sidestream smoke diffuses into the atmosphere, and the characteristic visible nature and odor thereof may be perceived negatively by some individuals. The relative amount of visible sidestream smoke generated by a burning cigarette is related to the amount of sidestream "tar" generated by that burning cigarette. Typical commercially available cigarettes which burn tobacco cut filler, and have lengths of about 84 mm (e.g., having a smokable rod length of about 57 mm and a filter element length of about 27 mm), often yield about 25 to about 35 mg of sidestream "tar" per cigarette. See, Proctor et al, Analyst, Vol. 113, p.
1509 (1988), for an apparatus and technique for determining the sidestream "tar" of a cigarette.
Numerous cigarettes which reportedly yield relatively low levels of visible sidestream smoke have been proposed. See, for example, U.S. Patent Nos.
4,637,410 to Luke; 4,624,268 to Baker et al: 4,407,308 to Baker; 4,231,377 to Cline et al; 4,420,002 to Cline;
4,450,847 to Owens; 4,108,151 to Martin; 4,225,636 to Cline; 4,433,697 to Cline; 4,461,311 to Mathews et al;
and 4,561,454 to Guess.
Through the years, there have been proposed various methods for altering the composition of mainstream tobacco smoke. For example, many tobacco substitute materials have been proposed, and a substantial listing of such materials can be found in U.S. Patent No.
4,079,742 to Rainer et al. ln addition, tobacco Y-119A-R&D:2 -~ tR~ ks A- substitute smoking materials having the tradcna~ Cytrel and NSM were introduced in Europe during the 1970's.
Numerous references have proposed articles which generate flavored vapor and/or visible aerosol. Most of 5 such articles have employed a combustible fuel source to provide an aerosol and/or to heat an aerosol forming material. See, for example, the background art cited in U.S. Patent No. 4,714,082 to Banerjee et al.
Smoking articles which are capable of providing the lo pleasures associated with cigarette smoking, by heating but not necessarily burning tobacco, and without delivering considerable quantities of incomplete combustion products, are described in U.S. Patent Nos.
4,714,082 to Banerjee et al; 4,756,318 to Clearman et al;
and 4,793,365 to Sensabaugh, Jr. et al. Such smoking articles employ a combustible fuel element for heat generation; and aerosol forming substances positioned physically separate from, and in a heat exchange relationship with, the fuel element. During use, heat 20 generated by the fuel element acts to volatilize the aerosol forming substances, thereby providing an aerosol which resembles tobacco smoke. Such smoking articles yield extremely low levels of visible sidestream smoke as well as low levels of FTC "tar".
It would be desirable to provide a good tasting cigarette which provides good smoking satisfaction, provides relatively low mainstream gas phase yields, provides relatively low levels of incomplete combustion products, sustains smolder during FTC smoking conditions, and generates low levels of sidestream "tar" and hence low levels of visible sidestream smoke.
Y-119A-R&D:3 ~ ~ 4 ~ 2026533 SUMMARY OF THE INVENTION
The present invention relates to smoking articles incorporating tobacco in cut filler form and/or in a processed form. Preferred smoking articles have the form of a cigarette having two essential components: (i) a roll or charge of smokable material, and (ii) an outer wrapping material (e.g., a paper wrapper) circumscribing the roll of smokable material. Cigarettes of the present invention incorporate a smokable filler material lo (described in greater detail hereinafter) as at least a portion of the smokable material thereof.
The preferred wrapping material, which surrounds the roll of smokable material to thereby form a "smokable rod", is a low air permeability cigarette paper wrapper.
Highly preferred wrappers having a low air permeability or low porosity exhibit a porosity below about 5 CORESTA
units. A CORESTA unit is a measure of the linear air velocity which passes through a 1 cm2 area of wrapper at a constant pressure of 1 centibar. See CORESTA Publication ISO/TC 126/SC I N159E (1986).
One form of smokable material is a tobacco-containing smokable filler material. Such a smokable material of the present invention comprises an intimate mixture of (i) tobacco (e.g., shredded tobacco laminae, pieces of tobacco stems, milled tobacco laminae, tobacco fines, tobacco dust, or a tobacco extract or other form of processed tobacco), and (ii) an agglomerated matrix filler having, in intimate contact, an organic component and an inorganic component. Preferably, the agglomerated matrix filler is provided in particulate form. The organic component is an alginate or other organic material capable of providing an agglomerated matrix filler which is essentially insoluble in water at ambient conditions. Normally, the inorganic component is calcium Y-119A-R&D:4 2026~39 -carbonate. The smokable filler material includes a binding agent in intimate contact with the agglomerated matrix filler and tobacco. As such, the binding agent acts to maintain particles of the tobacco and agglomerated matrix filler together to form the smokable filler material. Such a tobacco-containing smokable filler material also can include certain flavoring agents (e.g., cocoa, licorice, organic acids, menthol, and the like) and/or aerosol forming materials (e.g., glycerin, propylene glycol, and the like) in intimate contact therewith. The tobacco-containing smokable filler material can be cast as a sheet from an aqueous slurry, provided as a sheet using a paper-making process, or provided in extruded form. Such a tobacco-containing smokable filler material can be employed individually as the sole smokable material of the cigarette, or that tobacco-containing smokable filler material can be physically mixed with (i.e., blended) or otherwise employed with other smokable materials, such as tobacco cut filler.
Another form of smokable filler material of the present invention comprises an intimate mixture of agglomerated matrix filler having, in intimate contact, an organic component and an inorganic component.
Preferably, the agglomerated matrix filler is provided in particulate form. The organic component is an alginate or other organic material capable of providing an agglomerated inorganic filler material which is essentially insoluble in water at ambient conditions.
Normally, the inorganic component is calcium carbonate.
The smokable filler material includes a binding agent in intimate contact with the agglomerated matrix filler. As such, the binding agent acts to maintain particles of agglomerated matrix filler together to form the smokable filler material. Such a smokable filler material also Y-119A-R&D:5 -6- ~6~39 can include certain flavoring agents and/or aerosol forming materials in intimate contact therewith. The smokable filler material can be cast as a sheet from an aqueous slurry, provided as a sheet using a paper-making process, or provided in extruded form. Such a smokable filler material can be physically mixed with or otherwise employed with tobacco-cont~i n ing smokable materials and/or tobacco cut filler.
Nore specifically, a smokable filler material for a cigarette according to the invention may have incorporated therein an intimate mixture of agglomerated matrix filler having an inorganic component, and tobacco. The agglomerated matrix filler may be in an agglomerated form having particles of inorganic filler component spaced within a continuous or semi-continuous phase of organic component prior to formation of the intimate mixture.
In another aspect, a smokable filler material for a cigarette may have incorporated therein agglomerated matrix filler having an inorganic filler component and organic component. The agglomerated matrix filler may be in an agglomerated form having particles of inorganic filler component spaced within a continuous or semi-continuous phase of organic component prior to formation of the smokable filler material.
According to a further aspect of the invention, a smokable filler material for a cigarette may have incorporated therein an intimate mixture of (i) agglomerated matrix filler having particles of inorganic component spaced within a continuous or semi-continuous phase of an organic binding component, the agglomerated matrix filler being essentially insoluble in water at ambient conditions, and (ii) tobacco; the agglomerated matrix filler being in an agglomerated form prior to formation of the intimate mixture.
-6a- 2026539 According to a still further aspect of the invention, a smokable filler material for a cigarette may have incorporated therein agglomerated matrix filler having particles of inorganic component spaced within a continuous or semi-continuous phase of an organic binding component, the agglomerated matrix filler being essentially insoluble in water at ambient conditions, and being in an agglomerated form prior to formation of the smokable filler material.
BRIEF DESCRIPTION OF THE DRAWINGS
Figures 1 through 4 are longitudinal sectional views of smoking articles of the present invention.
DETATT.~D DESCRIPTION OF THE PREFERRED EMBODIMENTS
A preferred embodiment of a cigarette and smokable filler material of the present invention is shown in Figure 1. The cigarette 10 includes a generally cylindrical rod 15. The rod includes a roll of smokable material 20 wrapped in at least one layer of circumscribing outer wrapping material 25 (e.g., paper). The rod 15 is hereinafter referred to as a "smokable rod". The ends of the smokable rod are open to exposed the smokable material which is to be burned. The smokable rod is used by lighting one end thereof, and aerosol (e.g., smoke) is provided as a result of the combustion of the burning smokable material. As such, the smokable rod burns from the lit end thereof towards the opposite end thereof.
The cigarette 10 also includes a filter element 30 positioned adjacent one end of the smokable rod 15 such that the filter element and smokable rod are axially aligned in an end-to-end relationship, preferably abutting one another. Filter element 30 has a generally cylindrical shape, and the diameter thereof is essentially equal to the diameter of the smokable rod.
The ends of the filter element are open to permit the passage of air and smoke therethrough. The preferred filter element has at least two filter segments. As shown in Figure 1, a first filter segment is positioned adjacent the smokable rod, and preferably includes a carbonaceous filter material 35 circumscribed by a wrapping material 37; while a second filter segment is positioned at the extreme mouthend of the cigarette, and preferably includes a filter material 40, such as a gathered non-woven polypropylene web or cellulose acetate tow, circumscribed by a wrapping material 45. The filter material 40 of the segment preferably is a material which provides an aesthetically pleasing, white appearance.
Each of the filter segments is manufactured using known filter rod making machinery. The two segments are combined using known plug tube combining techniques, and are held together using circumscribing wrap 50 so as to form the filter element.
The filter element 30 normally is attached to the smokable rod 15 by tipping material 55, which circumscribes both the entire length of the filter element and an adjacent region of the smokable rod. The inner surface of the tipping material 55 is fixedly secured to the outer surface of the plug wrap 50 and the outer surface of the wrapping material 25 of the smokable rod, using a suitable adhesive. The cigarette 10 can be manufactured using known cigarette making techniques and equipment. Optionally, a ventilated or air diluted cigarette is provided with an air dilution means such as a series of perforations 65 which extend through the tipping material 55, plug wrap 50 and wrapping material 37. Such ventilation can be provided to the cigarette Y-119A-R&D:7 using known techniques, such as laser perforation techniques.
Another preferred embodiment of a cigarette and smokable filler material of the present invention is shown in Figure 2. The cigarette 10 is generally similar to the cigarette described with reference to Figure 1, except that the smokable material has the form of a blend which is provided in a segmented fashion. At one end of the smokable rod 15 (i.e., at the end of the cigarette to lo be lit) is located a first segment 70 of smokable material. At the other end of the smokable rod 15 (i.e., at the end of the smokable rod adjacent the filter element) is located a second segment 75 of smokable material. Each segment is defined or identified in terms of its composition (i.e., the composition of each segment is different). The segments are aligned in an abutting, end-to-end relationship; however, there can be a certain amount of intermixing of smokable materials in the region where the two segments meet. The length which each segment of smokable material extends along the smokable rod can vary. However, the relative longitudinal length of the first segment relative to the second segment normally ranges from about 1:2 to about 2:1, with about 1:1 being preferred. Such smokable rods can be manufactured using apparatus described in U.S. Patent Nos. 4,009,722 to Wahle et al and 4,516,585 to Pinkham.
For preferred cigarettes of the type shown in Figure 2, the first segment 70 normally includes of tobacco in some type of smokable form. Such a form of tobacco includes tobacco cut filler (e.g., tobacco laminae, processed tobacco materials, volume expanded tobacco filler, reconstituted tobacco filler materials, and the like, and blends thereof), and blends thereof with other smokable materials. Examples of processed tobacco materials are deproteinated reconstituted tobacco Y-119A-R&D:8 materials described in U.S. Patent Nos. 4,887,618 to Bernasek et al and 4,941,484 to Clapp et al. Preferred cigarettes also have a second segment 75 which includes a smokable material or blend of smokable materials different in overall composition from the overall composition of the smokable material(s) of the first segment 70. The first segment 70 and/or the second segment 75 include at least one smokable filler material of the present invention.
Another preferred embodiment of a cigarette of the present invention is shown in Figure 3. The cigarette 10 is generally similar to the cigarette described with reference to Figures 1 and 2, except that the smokable material 20, which incorporates smokable filler material of the present invention is wrapped or contained in a processed tobacco sheet 80, or other inner wrapper material. The processed tobacco sheet 80 normally is a reconstituted tobacco sheet which is manufactured using a paper-making process, and a single layer of the sheet circumscribes the smokable material 20. The smokable material 20 wrapped in the processed tobacco sheet 80 is in turn wrapped in a single layer of circumscribing outer wrapping material 25 (e.g., cigarette paper).
Another preferred embodiment of a cigarette of the present invention is shown in Figure 4. The cigarette 10 is generally similar to the cigarette described with reference to Figures 1, 2 and 3, except that the filter element includes three segments. Segment 85, positioned between first filter material 35 and filter material 40, preferably is composed of a particulate matter such as Y-119A-R&D:9 activated carbon granules, magnesium silicate granules, silica gel particles, or the like.
The smokable material employed in the manufacture of the smokable rod can vary, and most preferably has the form of cut filler. As used herein, the term "cut filler" in referring to smokable materials is meant to include smokable materials which have a form suitable for use in the manufacture of smokable rods for cigarettes.
As such, cut filler can include smokable materials which are blended and are in a form ready for cigarette manufacture. Smokable materials normally are employed in the form of strands or shreds as is common in cigarette manufacture. For example, cut filler can be employed in the form of strands or shreds cut from sheet-like or "strip" materials. Such strip materials are cut into widths ranging from about 1/5 inch to about 1/60 inch, preferably from about 1/25 inch to about 1/35 inch.
Generally, the resulting strands or shreds have lengths which range from about 0.25 inch to about 3 inches. Cut filler also can have an extruded form (e.g., extruded strands) or other physically processed form.
The smokable rods of cigarettes of the present invention include smokable filler material of the present invention. The smokable filler material can be employed in cut filler form.
One preferred type of smokable filler material of the present invention comprises an agglomerated matrix filler including an agglomerated matrix of an organic component and an inorganic component in intimate contact.
The agglomerated matrix filler is in turn intimately mixed with a binding agent to provide the smokable filler material. Such a smokable filler material most preferably includes as part of the ultimate mixture, at least one aerosol forming material and/or at least one flavoring agent. If desired, other agents, which have Y-119A-R&D:10 the ability to alter the composition of the aerosol generated by the smokable filler material, can be incorporated into that smokable filler material. The agglomerated matrix filler normally includes about 2 to about 99, preferably about 5 to about 20 weight parts inorganic component for each weight part of organic component. Such a smokable filler material normally includes about 60 to about 90, preferably about 65 to about 85 weight percent agglomerated matrix filler; up to about 20, preferably about 2 to about 10 weight percent binding agent; up to about 20, preferably about 3 to about 15 weight percent aerosol forming material; and sufficient amounts of flavoring agent to provide the desired flavor characteristics. If desired, a carbonaceous material (e.g., pyrolyzed alpha cellulose) can be incorporated into the smokable filler material, usually in amounts of up to about 10, and sometimes up to about 30 weight percent, based on the total dry weight of the smokable filler material. However, such further carbonaceous material is not a necessary component of the smokable filler material, and the smokable filler material can be absent of such carbonaceous material.
Such a smokable filler material is combustible and can be employed with (e.g., blended with) another smokable material (e.g., tobacco cut filler) in order to provide a cigarette of the present invention.
One preferred type of tobacco-containing smokable filler material of the present invention comprises an agglomerated matrix filler including an agglomerated matrix of an organic component and an inorganic component, which agglomerated matrix filler is in turn intimately mixed with some form of tobacco and binding agent, to provide smokable filler material. Such a tobacco-containing smokable filler material preferably includes as part of the ultimate mixture, at least one Y-119A-R&D:ll - 12 _ 2026539 aerosol forming material and/or at least one flavoring agent. If desired, other agents, which have the ability to alter the composition of the aerosol generated by the smokable filler material, can be incorporated into that smokable filler material. The agglomerated matrix filler normally includes about 2 to about 99, preferably about 5 to about 20 weight parts inorganic component for each weight part of organic component. Such a tobacco-containing smokable filler material normally includes up to about 75, typically up to about 50 weight percent of some form of tobacco; up to about 80, preferably about 20 to about 60 weight percent agglomerated matrix filler; up to about 20, preferably about 2 to about 10 weight percent binding agent; up to about 20, preferably about 3 to about 15 weight percent aerosol forming material; and sufficient amounts of flavoring agent to provide desired flavor characteristics. If desired, a carbonaceous material (e.g., pyrolyzed alpha cellulose~ can be incorporated into the smokable filler material, usually in amounts of up to about 10, and sometimes up to about 30 weight percent, based on the total dry weight of the smokable filler material. However, such further carbonaceous material is not a necessary component of the smokable filler material, and the smokable filler material can be absent of such carbonaceous material. Such a smokable filler material is combustible and can be employed individually as the sole smokable material of a cigarette of the present invention.
Another preferred type of smokable filler material of the present invention comprises an agglomerated matrix filler of an organic component and an inorganic component. The agglomerated matrix filler is intimately mixed with a binding agent and at least one aerosol forming material to provide the smokable filler material.
Y-119A-R~D:12 Such a smokable filler material most preferably includes as part of the ultimate mixture, at least one flavoring agent and some form of tobacco. The agglomerated matrix filler normally includes about 2 to about 99 weight parts inorganic component for each part of organic component.
Such a smokable filler material normally includes up to about 20, preferably about 3 to about 15 weight percent binding agent; greater than about 20, preferably about 25 to about 80, more preferably about 30 to about 50 weight percent aerosol forming material; and less than about 80, preferably about 30 to about 70 weight percent filler component including the previously described agglomerated matrix filler. In particular, the filler component can include (i) all of the previously described agglomerated matrix filler, or (ii) a blend of the previously described agglomerated matrix filler with an inorganic filler material (e.g., precipitated calcium carbonate) and/or an organic filler material (e.g., tobacco).
Amounts of flavoring agent sufficient to provide the desired flavor characteristics to the smokable filler material can be incorporated into the smokable material.
If desired, a carbonaceous material (e.g., pyrolyzed alpha cellulose) can be incorporated into the smokable material, usually in amounts of up to about 10, and sometimes up to about 30 weight percent, based on the total dry weight of the smokable material. However, such further carbonaceous material is not a necessary component of the smokable material, and the smokable material can be absent of such carbonaceous material.
The smokable filler material is combustible and can be blended with other smokable materials.
The tobacco-containing smokable filler materials of the present invention have some form of tobacco incorporated therein during its manufacture. The tobacco which is employed to provide such a tobacco-containing Y-119A-R&D:13 `~ - 14 - 202653~
smokable filler material can have a variety of forms, including tobacco extracts, tobacco fines or dust, shredded or comminuted tobacco laminae, tobacco stems, volume expanded tobacco filler and other forms of processed tobacco, and the like, and combinations thereof. Tobacco extracts are processed forms of tobacco and are provided by extracting a tobacco material using a solvent such as water, carbon dioxide, a hydrocarbon, or a halocarbon, as well as various other organic and inorganic solvents. Tobacco extracts can include spray dried extracts; freeze dried extracts; heat treated extracts; tobacco essences, such as those essences described in European Patent Publication No. 0326370 published August 2, 1989; and aroma oils and extracts described in U.S. Patent No. 4,506,682 to Mueller and Canadian Patent Application No. 596,617 filed April 13, 1989.
The smokable filler materials of the present invention incorporate a binding agent. Examples of suitable binding agents include hydroxypropylcellulose such as Klucel H from Aqualon Co.; hydroxypropyl-methylcellulose such as Methocel K4MS from The Dow Chemical Co.; hydroxyethylcellulose such as Natrosol 250 MRCS from Aqualon Co.; microcrystalline cellulose such as Avicel from FMC; methylcellulose such as Methocel A4M
from The Dow Chemical Co.; and sodium carboxymethyl-cellulose such as CMC 7HF and CMC 7H4F from Hercules Inc.
Especially preferred binding agents include the alginates, such as ammonium alginate, sodium alginate, propylene glycol alginate and potassium alginate. The alginates, and particularly the high viscosity alginates, can be employed in conjunction with controlled levels of free calcium ions. Other binding agents include starches Y-119A-R&D:14 -- 15 - 2026~39 (e.g., corn starch), carrageenan, guar gum, locust bean gum, pectins and xanthan gum. Combinations or blends of binding agents (e.g., a mixture of guar gum and locust bean gum) can be employed.
The smokable filler materials of the present invention can have at least one aerosol forming material and/or at least one flavoring agent incorporated therein.
The preferred aerosol forming materials include polyols (e.g, glycerin, propylene glycol or triethylene glycol), and any other materials which yield a visible aerosol, or combinations thereof. The aerosol forming material can be provided as a portion of the binding agent (e.g., when the binding agent is propylene glycol alginate).
Combinations of aerosol forming materials can be employed. The flavoring agents can vary, and include menthol, vanillin, citric acid, malic acid, cocoa, licorice, and the like, as well as combinations thereof.
See, Leffingwell et al, Tobacco Flavoring for Smoking Products (1972).
It is sometimes desirable to incorporate a caramelizing material into the smokable filler materials of the present invention. Caramelizing materials can act to improve (i) the integrity of the ash and fire cone of the cigarette, (ii) the appearance of the smokable filler material, and (iii) the flavor characteristics of the mainstream smoke of the cigarette. The caramelizing material can be incorporated into the smokable filler material during the preparation of that material and/or applied to the surface of that material (e.g., as a powder) after the manufacture thereof. Normally, the amount of caramelizing material which is employed to treat a particular smokable filler material is such that the resulting material which incorporates the caramelizing material includes up to about 20 weight parts of caramelizing material and greater than about 80 Y-119A-R&D:15 weight parts of the smokable material which is treated.
Examples of suitable caramelizing materials include sugars, such as glucose, fructose and sucrose; and compositions such as Carob Powder Code 1739 from M. F.
Neal, Inc.
The smokable filler materials of the present invention can be surface treated with certain substances.
For example, the smokable filler materials can have powdered substances applied to the surface thereof.
Exemplary substances include cocoa powder, licorice powder, powdered inorganic materials (e.g., potassium carbonate or iron oxide), tobacco dust, finely divided tobacco laminae, or the like, or blends thereof. The surface treatment of the smokable filler materials can provide to those materials improved color and appearance, improved as characteristics, and improved flavor characteristics.
The agglomerated matrix filler has an inorganic component and an organic component. For example, calcium carbonate agglomerated using an alginate has an inorganic component and an organic component. Other inorganic components include calcium sulfate, magnesium oxide and magnesium carbonate. Ammonium alginate is an especially preferred alginate. Such an agglomerated matrix filler can be provided by preparing an aqueous slurry of calcium carbonate particles and hydrated alginate, and drying the slurry to form an agglomerated matrix of calcium carbonate (i.e., a matrix of a plurality of calcium carbonate particles spaced within a continuous or semi-continuous phase of alginate). If desired, the slurrycan be volume expanded by incorporating a foaming agent therein. Examples of suitable foaming agents include linear sodium benzene sulfonates, linear alkyl sulfates and linear alkyl ethoxy sulfates. Preferably, a high solids content aqueous slurry of calcium carbonate and Y-119A-R&D:16 alginate is spray dried to provide agglomerated particles (e.g., normally spherical particles) of calcium carbonate particles and alginate. Alternatively, the slurry can be dried by the application of heat to provide a solid mass of agglomerated calcium carbonate and alginate, and the solid mass can be ground to yield particles of the desired size. Preferably, the amount of calcium carbonate relative to alginate ranges from about 99:1 to about 2:1, preferably about 20:1 to about 5:1, on a dry lo weight basis. Typically, the particles of calcium carbonate agglomerated using alginate are essentially insoluble in water under ambient conditions. In particular, the essentially insoluble character of the alginate in the agglomerated matrix filler tends to limit to a great degree any propensity of the agglomerated matrix filler to lose its agglomerated character when contacted with water under ambient conditions. The agglomerated matrix filler is rendered insoluble due to the interaction of the alginate with calcium ions of the calcium carbonate. If desired, the agglomerated matrix filler can be treated with a dilute solution of acid to decompose a portion of the calcium carbonate and the resulting calcium ions can act to render insoluble the alginate component of the agglomerated matrix filler.
The agglomerated matrix filler having an inorganic component and an organic component can incorporate a variety of other organic components. For example, the organic component can be pectin, which has a tendency to become essentially water insoluble upon interaction with calcium ions. Alternatively, agglomerated matrix filler having a polysaccharide organic component can be treated with divalent ions (e.g., calcium, barium, cobalt, iron or manganese ions) or trivalent ions (e.g., iron or aluminum ions) to render the polysaccharide essentially water insoluble. As yet another example, a slurry of Y-119A-R&D:17 - 202653~
polysaccharide material (e.g., ethylcellulose) and inorganic component particles can be provided in a non-aqueous solvent (e.g., alcohol) and dried, resulting in the formation of an agglomerated matrix filler which is essentially water insoluble.
Other inorganic materials can be incorporated as fillers in the smokable filler materials of the present invention. Such inorganic materials often have a fibrous, flake, crystalline, amorphous, hollow or particulate form. Examples of inorganic filler materials include calcium carbonate, calcium sulfate particles, magnesium oxide, magnesium hydroxide, perlite, synthetic mica, vermiculite, clays, thermally stable carbon fibers, zinc oxide, dawsonite, low density hollow spheres of calcium carbonate, glass spheres, glass bubbles, thermally stable carbon microspheres, calcium sulfate fibers, hollow ceramic microspheres, alumina, calcium carbonate particles agglomerated using a carbonaceous component, low density processed calcium carbonate, and the like.
The agglomerated matrix filler has the form of an agglomerated matrix of an inorganic component and a carbonaceous component. The inorganic component thereof can include particles of calcium carbonate, calcium sulfate, magnesium oxide, magnesium carbonate, and the like. A particularly preferred agglomerated matrix filler is agglomerated calcium carbonate, and most preferably, agglomerated precipitated calcium carbonate.
Such an agglomerated matrix filler is prepared by providing an aqueous slurry of calcium carbonate particles and a binding material, and drying the slurry to form an agglomerated matrix of calcium carbonate (i.e., a matrix of a plurality of calcium carbonate particles spaced within a continuous or semi-continuous phase of binding material). Calcium carbonate particles Y-119A-R&D:18 which are employed to provide the agglomerated matrix typically exhibit a surface area of less than about 20 m2/g, frequently less than about 10 m2/g, and sometimes less than about 1 m2/g, as determined using the Brunauer, Emmett and Teller (BET) method described in J. Am. Chem.
Soc., Vol. 60, p. 309 (1938). Typical binding materials are organic materials, such as cellulosic derivatives (e.g., sodium carboxymethylcellulose), and preferably are sugar containing materials, such as molasses, high fructose corn syrup, or Carob Powder Code 1739 from M. F.
Neal, Inc. Other organic materials, such as pectins, alginates and the other previously described organic materials, also can be employed.
Preferably, a high solids content aqueous slurry (e.g, about 40 to about 55 weight percent solids content slurry) of calcium carbonate and binding material is spray dried to provide agglomerated particles (e.g., normally spherical particles) of calcium carbonate particles and binding material. Alternatively, the slurry can be dried by the application of heat to provide a solid mass of agglomerated calcium carbonate and binding material, and the solid mass can be ground to yield particles of the desired size. Preferably, the amount of calcium carbonate relative to binding material ranges from about 20:1 to about 2:1, more preferably about 15:1 to about 4:1, on a dry weight basis.
Normally, the inorganic particles agglomerated using saccharide and polysaccharide materials tend to lose their agglomerated character when contacted with water under ambient conditions, as a result of the propensity of the saccharide and polysaccharide materials to be soluble in water.
The agglomerated matrix of inorganic component and organic binding material is subjected to heat treatment.
As such, volatile components from the organic binding Y-119A-R&D:19 ~ - 20 - 202653~
material are expelled, and the organic binding material is calcined to form an essentially water insoluble, clean burning carbonaceous component. Normally, the heat treatment of the agglomerated matrix filler is provided under controlled atmosphere, in order to minimize or prevent oxidation of the binding material. Preferably, the heat treatment provides a binding material which is in the form of a carbonaceous material, and in turn, provides a means for agglomerating the particles of inorganic component into a matrix form. In particular, the particles of agglomerated calcium carbonate and binding material can be heat-treated (e.g., to a temperature of up to about 625C, and usually up to about 600C) using an oven, a fluidized bed, rotary calciner, belt calciner, or the like. For example, particles of spray dried calcium carbonate particles agglomerated using molasses can be heated in a fluidized bed having gaseous nitrogen flowing therethrough, heated at temperatures sufficient to heat the particles to about 300C to about 625C, and collected. The agglomerated matrix of inorganic component and organic binding material can be subjected to heat treatment sufficient to calcine the organic binding material by subjecting the agglomerated matrix to very high temperatures (e.g., up to about 900C) for a short time period and under conditions sufficient to avoid decomposition of the inorganic component (e.g., when the inorganic component is calcium carbonate). However, if the inorganic component is calcium carbonate, and the calcium carbonate undergoes some decomposition during the calcining step, the agglomerated material can be re-carbonated by (i) exposing that material to carbon dioxide atmosphere, or Y-119A-R&D:20 ~026539 (ii) dispersing that material in water and bubbling carbon dioxide into the dispersion.
After the calcining process, the agglomerated calcium carbonate particles normally have a calcium carbonate content of greater than about 80, frequently greater than about 90 weight percent and a carbon content of greater than about 3 weight percent. Normally, the resulting agglomerated particles are screened to sizes of about -50/+325 US Mesh, and often about -80/+200 U.S.
Mesh. Preferred agglomerated calcium carbonate particles which have been calcined are essentially insoluble in water, are spherical in shape, are free flowing, and exhibit a bulk density of about 0.1 g/cm3 to about 1.1 g/cm3, frequently about 0.3 g/cm3 to about 1 g/cm3~, using mercury intrusion techniques. As such, calcined agglomerated calcium carbonate particles provide an inorganic material having a bulk density less than about 2 g/cm3, and preferably less than about 1 g/cm3, which includes an inorganic component having a bulk density greater than about 2.5 g/cm3. Normally, such calcined agglomerated calcium carbonate particles exhibit a surface area of less than about 30 m2/g, and often about 10 m2/g to about 25 m2/g, as determined using the BET
method.
If desired, the bulk density of the calcined agglomerated inorganic filler can be lowered by digesting away part of the inorganic component with an acidulant.
For example, calcined agglomerated can be dispersed in water, and an aqueous hydrochloric acid solution can be added to the resulting slurry which is agitated. The acid reacts with the calcium carbonate, and essentially does not react with the carbonaceous component. Thus, the carbonaceous component acts to hold together the remaining calcium carbonate, while a portion of the Y-119A-R&D:21 calcium carbonate reacts to produce carbon dioxide gas and water soluble calcium chloride.
Another type of inorganic material which can be incorporated into smokable filler materials of the S present invention is a low density inorganic filler.
Such a filler is provided by providing particles of a calcium salt, decomposing the anion of the salt and contacting the particles with carbon dioxide. Examples of suitable salts include calcium propionate, succinate, tartrate, stearate, salicylate, palmitate, oleate, lactate, gluconate, citrate, ascorbate, acetylsalicylate and benzoate. Other suitable salts include calcium salts of saccharides and polysaccharides. Such salts are subjected to conditions sufficient to decompose the anion thereof, which usually involves subjecting the salt to heat treatment under carbon dioxide atmosphere.
One method for providing a low density inorganic filler involves heating calcium lactate particles screened to -80/+170 US Mesh at about 600C for about 8 hours under a steady 228 ml/min. flow of carbon dioxide gas, so as to provide a material which has undergone about a 65 percent weight loss. About 20 weight parts of the material is charged into about 80 weight parts water and the resulting slurry is contacted with sufficient hydrochloric acid solution to lower the pH thereof to about 6.8. The material then is removed from the water, washed with water, dried, and screened to a particle size of -80/+170 US Mesh. Such material is greater than about 95 weight percent calcium carbonate, and exhibits a bulk density of about 0.4 g/cm3, as determined using mercury intrusion techniques.
Typically, the smokable filler materials of the present invention are provided by forming an aqueous slurry of binding agent and the other components of that smokable filler material, casting the slurry as a sheet, Y-119A-R&D:22 _ - 23 - 2026539 and drying the cast material to form a relatively dry, workable sheet. Techniques and equipment for casting a slurry as a sheet will be apparent to the skilled artisan. Other materials, such as calcium acetate, potassium carbonate, pH control agents, urea, amino acids, potassium chloride and/or calcium hydroxide, can be incorporated into the slurry. Sequestering agents (e.g., diammonium hydrogen orthophosphate, sodium citrate, potassium hexametaphosphate or tetrasodium pyrophosphate) can be incorporated into the slurry in amounts sufficient to control the free calcium ion concentration of the slurry. The cast material can be dried at ambient temperatures or at elevated temperatures. Further, an aqueous solution of calcium salts can be applied to the cast slurry. The resulting dried sheet can be cut or broken into "strip" form, and later can be cut or shredded into cut filler form.
The smokable filler materials of the present invention can be provided using a paper-making process. In particular, an aqueous slurry of a cellulosic material (e.g., softwood pulp, hardwood pulp, flax fibers and/or shredded tobacco stems) and the previously described filler can be cast as a mat on a fibrous belt or wire screen, and dried to the desired moisture level.
Normally, a slurry, dispersion or solution of flavoring agents, tobacco extracts, tobacco parts, aerosol forming materials, and the like, can be applied to the mat (e.g., as a spray), and the resulting mat can be dried further to form a sheet. The resulting dried sheet can be cut or broken in "strip" form, and later can be cut or shredded into cut filler form. Techniques and equipment for making a paper-type sheet will be apparent to the skilled artisan.
The smokable filler materials of the present invention can be extruded into the desired shape using Y-119A-R&D:23 suitable extrusion techniques. See, for example, the types of processes described in U.S. Patent No.4,880,018 to Graves, Jr. et al. Alternatively, an aqueous slurry of the components of the smokable and an alginate binding agent can be extruded into an aqueous solution of calcium ions (e.g., an aqueous solution of calcium chloride), collected and dried. If desired, extruded smokable filler materials can be physically processed (e.g., subjected to treatment using rollers, etc.) and formed into the desired shape.
The smokable rods of cigarettes of the present invention often include a physical mixture or blend of smokable materials. The blend can include two or more smokable filler materials of the present invention, or a physical mixture of at least one smokable filler material of the present invention with at least one other smokable material. Certain preferred cigarettes often include within such a blend, a sufficient amount of at least one of the smokable filler materials of the present invention such that the smokable material within each cigarette comprises at least about 1 percent of the carbonaceous material, based on the total weight of the blend. In particular, cigarettes having such types of smokable filler materials and having low porosity paper outer wrappers (e.g., having outer wrappers having less than about 5 CORESTA units) have the propensity to sustain smolder (e.g., not self-extinguish), when smoked under FTC smoking conditions. FTC smoking conditions consist of 35 ml puffs of 2 second duration, taken every 60 seconds.
The smokable filler materials of the present invention can be blended with tobacco cut filler. The type of tobacco can vary, and can include flue-cured, Burley, Maryland and Oriental tobaccos, as well as the Y-119A-R&D:24 2026~39 rare and specialty tobaccos, and blends thereof. Such tobacco cut filler can be provided in the form of tobacco laminae; volume expanded or puffed tobacco laminae;
processed tobacco stems such as cut-rolled or cut-puffed stems; reconstituted tobacco materials, such as (i) deproteinated tobacco materials described in U.S. Patent Nos. 4,887,618 to Bernasek et al and 4,941,484 to Clapp et al, (ii) a phosphate-containing reconstituted tobacco material described in U.S. Patent Nos. 3,353,541 and 3,420,241 to Hind et al, and 3,386,449 to Hind, (iii) a reconstituted tobacco material described in Tobacco Encyclopedia, edit. by Voges, p. 389, TJI (1984), or blends thereof.
Smokable materials can be cased and top dressed as is conventional during various stages of cigarette manufacture. For example, flavoring agents can be applied to the smokable material as is commonly performed - when cigarette cut filler is processed. Suitable flavoring agents include vanillin, cocoa, licorice, menthol, and the like. Flavor modifying agents can be applied to the smokable material. A flavor modifying agent in the form of levulinic acid can be applied to the smokable filler material (e.g., in amounts ranging from about 0.01 to about 2 percent, normally from about 0.1 to about 1 percent, preferably about 0.2 to about 0.6 percent, based on the dry weight of the smokable material). Another flavor modifying agent in the form of potassium carbonate can be applied to the smokable material (e.g., in amounts of less than about 5 percent, Y-119A-R&D:25 - 26 - 2026~39 normally about 2 to about 3 percent, based on the dry weight of the smokable material). Aerosol forming materials and humectants, such as glycerin and propylene glycol, can be applied to the smokable material. Such components conveniently are applied to the smokable material as casing and top dressing components.
The preferred wrapping material which provides the smokable rod is a cigarette wrapping material having a low air permeability value. Such a wrapping material normally has an air permeability of less than about 5 CORESTA units, often less than about 3 CORESTA units, and frequently less than about 1 CORESTA unit. Typical wrapping materials are cigarette paper wrappers.
Suitable wrapping materials are cigarette paper wrappers available as DD-71-1, DD-71-6, MTR-1021, P-2831-60-2, P-2831-60-3, P-2831-60-4, P-2831-60-5, P-2674-110, P-2831-60-1 and DD-100-2 from Kimberly-Clark Corp.
Suitable low porosity cigarette paper wrappers are commercially available, and can have various levels of burn chemicals, fluxing agents, etc., incorporated therein. Particularly preferred are cigarette paper wrappers which include an amount of a polymeric film forming agent sufficient to provide a paper having the desirably low air permeability value. For example, a sufficient amount of a solution of a polymeric (e.g., carboxymethyl cellulose or ethylcellulose) film forming agent can be applied to a paper wrapper. The selection of the polymeric film forming agent will be apparent to the skilled artisan.
The optional polymeric film forming agent can be applied to the paper wrapper during the manufacture of the paper, or applied as a print or paint after manufacture of the paper is complete. Typically, the film forming agent is applied to the paper as a dilute solution (e.g., at a concentration of about 0.2 to about Y-119A-R&D:26 ~ - 27 - 2026539 5 weight percent relative to the solvent) for ease of processing. The amount of film forming agent applied to the paper wrapper depends upon factors such as the permeability of the paper and the film forming capabilities of the film forming agent. Typically, the amount of film forming agents employed ranges from about 1 to about 10 percent, based on the dry weight of the paper. For example, a 5 weight percent solution of ethylcellulose in ethanol or sodium carboxymethyl-cellulose in water can be applied to cigarette paperusing a size press, and the paper can be dried to provide a non-wetting, moisture resistant paper wrapper having a porosity of less than about 1 CORESTA unit, preferably less than about 0.5 CORESTA unit.
The smokable rods and the resulting cigarettes can be manufactured in any known configuration using known cigarette making techniques and equipment. Smokable rods often include smokable material wrapped in a single layer of wrapping material, although a double layer of two types of wrapping materials can be employed.
Cigarettes having smokable rods which are double wrapped with two layers of wrapping material preferably include one of the previously described low porosity paper wrappers as the outer wrappers. The inner wrapper can vary, but typically is a tobacco-containing wrapping material. Exemplary inner wrappers are paper wrappers which include about 3 parts Java tobacco stem parts and about 1 part wood pulp, and are available from Kimberly-Clark Corp. as P-2249-115 and P-2831-23-3.
Other suitable inner wrapping materials include tobacco parts and carbonaceous materials, and are available from Kimberly-Clark Corp. as P-2540-94-A, P-2540-94-C and Y-119A-R&D:27 - 2026~39 P-2540-94-D. The inner wrapping materials (i) can include burn chemicals (e.g., potassium citrate, potassium acetate or potassium succinate), and/or (ii) act as a substrate for flavors (e.g., menthol or vanillin) or flavor precursors (e.g., vanillin glucoside or ethylvanillin glucoside).
Typically, the smokable rod has a length which ranges from about 30 mm to about 70 mm, preferably about 35 to about 60 mm; and a circumference of about 17 mm to about 27 mm, preferably about 22 mm to about 25 mm.
Short smokable rods (i.e., having lengths from about 30 to about 50 mm) can be employed, particularly when smokable materials having a relatively high packing density are employed.
The packing density of the smokable material contained within the outer wrapping material can vary.
Typical packing densities for smokable rods of cigarettes of the present invention range from about 150 to about 400 mg/cm3. Normally, packing densities of such smokable rods range from about 200 to about 380 mg/cm3, frequently about 250 to about 360 mg/cm3, particularly when relatively short (i.e., less than 50 mm long) smokable rods are employed.
The cigarettes of the present invention preferably include a filter element, and most preferably a filter element having more than one segment. For example, a preferred filter element has two or more filter segments.
Typically, the segments of the preferred filter elements each have lengths which ranges from about 10 mm to about 30 mm; and circumferences of about 17 mm to about 27 mm, preferably about 22 mm to about 25 mm. The plug wrap which circumscribes the filter material of each filter segment typically is a conventional paper plug wrap, and can be either air permeable or essentially air impermeable.
Y-119A-R&D:28 - 29 - 2026~39 Preferred filter materials of one of the filter ,egments include carbonaceous materials (e.g., activated carbon particles, charcoal particles, or carbon paper).
An example of a particularly preferred filter material is provided by gathering a tobacco/carbon paper available as P-144-BAC from Kimberly-Clark Corp. Such filter materials reduce the levels of certain gas phase components from the mainstream smoke which passes to the mouth of the smoker. As such, preferred filter materials of that segment act to reduce the levels of any smoke components which may provide an off-taste or other undesirable characteristics to the mainstream smoke.
Preferred filter materials of another of the filter segments normally include fibrous materials. An example of a suitable filter material is a gathered nonwoven polypropylene web. A particularly preferred nonwoven polypropylene sheet-like web is available as PP-100-F
from Kimberly-Clark Corp. Another example of a suitable filter material is a cellulose acetate tow. Particularly preferred cellulose acetate tow items include (i) 8 denier per filament/40,000 total denier, and (ii) 8 denier per filament/15,000 total denier, (iii) 8 denier per filament/25,000 total denier, and (iv) 8 denier per filament/30,000 total denier. Plasticizers, such as triacetin, propylene glycol or triethyl citrate, can be combined with the filler materials.
Another filter segment can have a filter material in the form of a gathered web of nonwoven thermoplastic (i.e., hydrophobic) fibers in intimate contact with a water soluble tobacco extract so as to provide an extract-containing filter material. A highly preferred web is a nonwoven web of polypropylene fibers available as PP 200 SD from Kimberly-Clark Corp. Such segments can Y-119A-R&D:29 _ - 30 - 2026539 provide enhanced flavor characteristics to the mainstream smoke which passes therethrough.
Yet another filter segment can include a tobacco paper material as the filter material. For example, a filter material can have the form of a gathered web of tobacco paper available as P-144-B from Kimberly-Clark Corp.
The filter element segments suitable for use in this invention can be manufactured using known cigarette filter making techniques. Filter elements can be manufactured from cellulose acetate tow using known techniques. Filter elements can be manufactured from carbon paper, tobacco paper and a sheet-like nonwoven polypropylene web using filter making techniques described in U.S. Patent No. 4,807,809 to Pryor et al.
Alternatively, particles of charcoal or activated carbon can be incorporated into the filter element using a so-called "triple filter" configuration by positioning the particles between two segments of suitable filter materials.
The filter elements can have low, moderate or high filtration efficiencies. Preferred filter elements have minimal mainstream aerosol (i.e., smoke) removal efficiencies while maintaining the desirable draw characteristics of the cigarette. Such minimal smoke removal efficiencies are provided by "low efficiency filter elements. Low efficiency filter elements have a minimal ability to remove mainstream smoke particulates.
See, Keith in Schemeltz's The Chemistry of Tobacco and Tobacco Smoke, p. 157 (1972). Generally, low efficiency filter elements provide less than about 40 weight percent mainstream smoke particulate removal efficiency.
Y-119A-R&D:30 `~ 2026539 Tipping material circumscribes the filter element and an adjacent region of the smokable rod such that the tipping material extends about 3 mm to about 6 mm along the length of the smokable rod. Typically, the tipping material is a conventional paper tipping material.
Tipping materials of varying porosities can be employed.
For example, the tipping material can be essentially air impermeable, air permeable, or treated (e.g., by mechanical or laser perforation techniques) so as to have a region of perforations, openings or vents thereby providing a means for providing air dilution to the cigarette. The total surface area of the perforations and the positioning of the perforations along the periphery of the cigarette can be varied in order to control the performance characteristics of the cigarette.
For air diluted or ventilated cigarettes of the present invention, the amount of air dilution can vary.
Typically, the amount of air dilution for an air-diluted cigarette is greater than about 25 percent, and frequently greater than about 40 percent. The upper limit for air dilution for a cigarette typically is less than about 75 percent, more frequently less than about 65 percent. As used herein, the term "air dilution" is the ratio (expressed as a percentage) of the volume of air drawn through the air dilution means to the total volume of air and aerosol (i.e., smoke) drawn through the cigarette and exiting the extreme mouthend portion of the cigarette. See, Selke et al, Beitr. Zur Tabak. In., Vol.
4, p. 193 (1978).
Cigarettes of the present invention, when smoked, provide a flavorful mainstream aerosol. The mainstream aerosol of such cigarettes can yield low levels of incomplete combustion products as well as low levels of gas phase components. The cigarettes burn at an acceptable rate, and maintain static smolder, at least Y-119A-R~D:31 when smoked under FTC smoking conditions. The cigarettes, when smoked, have an ash and fire cone which is not overly cohesive, and hence, is not overly long.
However, the cigarettes also provide an ash and fire cone which exhibit good integrity.
Cigarettes of the present invention, when smoked, generally yield less than about 20 mg, preferably less than about 10 mg of sidestream "tar" per cigarette, as determined using the apparatus and techniques described by Proctor et al, Analyst, Vol. 113, p. 1509 (1988).
Such cigarettes normally provide more than about 5 puffs, preferably more than about 6 puffs per cigarette, when smoked under FTC conditions. Normally, cigarettes of the present invention provide less than about 20 puffs, and often less than about 15 puffs, when smoked under FTC
conditions.
The following examples are provided in order to further illustrate the invention but should not be construed as limiting the scope thereof. Unless otherwise noted, all parts and percentages are by weight.
A. Preparation of a Tobacco-Containing Smokable Filler Material A filler is provided as follows:
Into a high shear blender is charged about 500 parts tap water and about 5 parts of a high viscosity ammonium alginate available as Amoloid HV from Kelco Division of Merck & Co., Inc. The resulting mixture is agitated at ambient temperature so as to disperse the alginate in the water and hydrate the alginate. Then, about 95 parts of precipitated calcium carbonate available as USP Light from Pfizer Inc. is added to the water/alginate mixture.
Y-119A-R&D:32 - 20265~9 The resulting slurry is agitated at moderate rate for about 10 minutes until a consistent slurry is provided.
The slurry is spray dried using an Anhydro Type Lab Sl spray dryer having an air atomized nozzle at an inlet temperature of about 290C and an outlet temperature of about 220F. The spray dryer is equipped with a Masterflex Pump System using a Model 7016-20 head supplied by Cole-Parmer Instrument Co. The nozzle air pressure is 4 psi, and the liquid feed rate is that provided by setting the pump speed control to 2. The resulting spray dried particles have a generally spherical shape. The particles are screened to a particle size of -80/+325 U.S. Mesh.
The spray dried particles are free flowing, are essentially insoluble in water at ambient temperature, resist wetting, and remain in an agglomerated state when contacted with water under ambient conditions. The particles each are an agglomerated matrix of a plurality of precipitated calcium carbonate particles spaced within an alginate.
The smokable material is provided as follows:
Into a high shear blender containing 225 parts tap water and set at low speed is charged about 5 parts of a high viscosity ammonium alginate available as Amoloid HV
from Kelco Division of Merck & Co., Inc. The resulting mixture is agitated at ambient temperature so as to disperse the alginate in the water and hydrate the alginate. Then, 20 parts glycerin and 25 parts tap water are charged into the water/alginate mixture. Then, 17.2 parts of the previously described agglomerated calcium carbonate is charged into the mixture. The resulting slurry is agitated until a consistent slurry is provided.
The slurry is cast to about a 0.025 inch thickness onto a high density polyethylene sheet and air dried.
The resulting sheet light brown color and a flexible Y-119A-R&D:33 ~026~39 _ character. The sheet is cut at 32 cuts per inch using a paper shredder.
The shreds of sheet are dusted with about 8.5 parts of finely divided Pennsylvania cigar tobacco laminae.
B. Preparation of a Cigarette Cigarettes substantially as shown in Figure 3 are provided as follows:
The cigarettes each have a length of about 84 mm and a circumference of about 24.8 mm, and include a smokable rod having a length of about 57 mm, a first filter segment having a length of about 15 mm and a second filter segment having a length of about 12 mm. The first and second filter segments form a filter element. Each filter segment is attached to each smokable rod using nonporous tipping paper. For each cigarette, the tipping paper circumscribes the filter element and about a 4 mm length of the smokable rod in the region adjacent the filter element. The filter elements are ventilated to about 60 percent air dilution by providing a ring of perforations through the tipping paper and plug wrap of the filter element circumscribing the cigarette about 12 mm from the extreme mouthend thereof.
The smokable rod includes the previously described tobacco-containing smokable material in cut filler form.
The first filter segment is provided by gathering a 11.75 inch wide web of tobacco and carbon paper available as (P-144-BAC) from Kimberly-Clark Corp. using the filter rod forming apparatus described in Example 1 of U.S.
Patent No. 4,807,809 to Pryor et al. The plug wrap for the filter segment is available as Reference No. 5831 from Ecusta Corp. The first filter segment is positioned adjacent the smokable rod.
Y-119A-R&D:34 The second filter segment is provided by gathering a 11.75 inch wide web of non-woven polypropylene web available as PP-100-F from Kimberly-Clark Corp. using the filter rod forming apparatus described in Example 1 of U.S. Patent No. 4,807,809 to Pryor et al. The plug wrap for the filter segment is available as Reference No. 5831 from Ecusta Corp. The second filter segment is positioned adjacent the first filter segment, at the extreme mouth end of the cigarette.
The cigarette outer paper wrapper exhibits an air permeability of about 0 CORESTA unit. The cigarette paper is available as P-2831-60-1 from Kimberly-Clark Corp.
The inner wrapper of the smokable rod is a tobacco-containing paper available as P-2831-23-3 from Kimberly-Clark Corp.
Smokable cigarette rods are provided using known techniques. In particular, the smokable material is circumscribed by a single layer of paper wrap. The weight of the smokable material within each cigarette rod is about 1 g.
The cigarettes are employed by burning the smokable rod such that the smokable material within the paper wrapper burns to yield smoke. When employed, such cigarettes yield very low levels of visible sidestream smoke and essentially no sidestream odor. The cigarettes do not self-extinguish during the smolder period experienced during FTC smoking conditions.
Particles of calcium carbonate agglomerated with an alginate are provided as follows:
Into a blender is charged about 750 ml tap water, and then about 20 g glycerin. While the mixture is Y-119A-R&D:35 -gently agitated, about 10 g of the ammonium alginate described in Example 1 is slowly added thereto, so as to disperse the alginate in the water. The resulting mixture is transferred into a 1 liter jar, sealed, and gently rolled overnight to hydrate the alginate.
A slurry of 250 g precipitated calcium carbonate available as Code No. 2A from Pfizer Inc. in 250 g tap water is provided. Then, the slurry is added to 200 g of the water/glycerin/alginate mixture. The resulting slurry is agitated gently so as to provide a slurry having a smooth texture.
The slurry is cast onto a high density polyethylene sheet at a thickness of about 0.04 inch, and air dried to provide pieces of dried sheet about 6 inches by about 6 inches in size. The resulting dried sheet is hand ground to a fine particle size and screened to -50 US Mesh.
Particles of calcined agglomerated calcium carbonate are provided as follows:
Into a low shear mixer are charged about 832 parts tap water at ambient temperature, about 757 parts precipitated particulate calcium carbonate available as Albacar 5970 from Pfizer Inc., and about 267 parts molasses. The calcium carbonate has a rosettic structure and an average particle size (i.e., diameter) of about 2 microns. The molasses is available as Refiner's Syrup from Savannah Sugar Co., and has a solids/water content of about 3.7:1. The resulting mixture is agitated for about 5 to about 10 minutes to provide a slurry having a solids content of about 52 percent and a viscosity of about 1,200 cps as measured by a Brookfield LVT
viscometer with cylindrical LV spindle No. 4.
The slurry is spray dried by continuously pumping the slurry at about 6 lbs./min. at a feed pressure of about 475 to about 500 psig to a spray dryer. The spray dryer is a Bowen Type commercial unit equipped with an Y-119A-R&D:36 SD-046 nozzle, and operated in a commercial mode. The inlet temperature is about 470F, and the outlet temperature is about 260F. The resulting spray dried particles have a generally spherical shape, and a moisture content of below about 2 percent. The particles are screened to a particle size of -70/+200 US Mesh.
The spray dried particles are placed on a 12 inch by 36 inch steel tray to a thickness of about 0.5 inch. The tray then is passed into a continuous belt furnace at a rate of about 8 to about 12 inches/min., and is subjected to heating under nitrogen atmosphere at above about 600C
for about 10 minutes, and at above about 400C for about 20 minutes. The oven is set at about 720C, and the tray is subjected to a maximum air temperature of about 670C
during that time. The heated particles are removed from the furnace into a cooling zone for about 1 hour under nitrogen atmosphere, and cooled to ambient temperature.
The calcined particles so collected are black, are spherical in shape, are free flowing, and resist wetting.
The particles are about 93 percent calcium carbonate, and exhibit a bulk density of about 0.5 g/cm3. The particles each are an agglomerated matrix of a plurality of precipitated calcium carbonate particles spaced within a carbonaceous material.
A tobacco-containing smokable filler material is prepared as follows:
Into a high shear blender is charged about 225 ml tap water, and into the water is dispersed about 5 g of the ammonium alginate described in Example 1. The resulting mixture is gently agitated at ambient temperature for about 15 minutes, until the alginate is hydrated. Then, about 20 g glycerin is added to the mixture, followed by about 25 ml tap water. To the mixture is added about 16.7 g of an "American blend" of tobacco cut filler which has been ground to a powder.
Y-119A-R&D:37 Then, about 25 ml tap water is added to the mixture. The resulting mixture is agitated until a smooth slurry results. To the slurry is added a mixture of about 13.8 g of the calcined agglomerated calcium carbonate and about 13.8 g calcium carbonate agglomerated with ammonium alginate. The resulting slurry is agitated until the slurry exhibits a smooth texture. The resulting slurry is cast onto a high density polyethylene sheet at a thickness of about 0.025 inch and air dried.
A. Preparation of an Agglomerated Matrix Filler Into about 500 parts tap water at ambient temperature and maintained at high shear in a blender is charged about 5 parts ammonium alginate available as Amoloid HV. The mixture is agitated until the alginate is fully hydrated. The mixture is then transferred to an egg beater type mixer. Then, about 94.5 parts precipitated calcium carbonate, as described in Example 1, is charged into the mixture. Agitation is continued until the mixture achieves a smooth consistency. Then about 0.5 parts sodium dodecyl sulfate, from Aldrich Chemical Co., is charged into the mix. Agitation is continued for about 15 minutes at which time the mixture foams.
The slurry is cast to about a 0.05 inch thickness onto a high density polyethylene sheet and air dried.
The resulting sheet is white and very brittle. It is ground and sieved to obtain a -30/+lO0 US Mesh particle size fraction. This material does not lose its structure when emersed in water. This is because the binder has become water insoluble. The material has a tap density, as measured with a graduated cylinder, of about Y-119A-R&D:38 0.26 g/cm3. The tap density of the original calcium carbonate, measured by the same method, is about 0.46 g/cm3.
B. Preparation of a Smokable Filler Material Into about 200 parts tap water at ambient temperature and maintained at high shear in a blender is charged about 3.33 parts ammonium alginate as Amoloid HV
and then about 4.5 parts glycerin. The mixture is agitated for about 15 minutes until the components are fully hydrated. The mixture is then transferred to an egg beater type mixer and agitated. Separately, about 60 parts of the above described agglomerated calcium carbonate is mixed with about 400 parts tap water and the resulting slurry is added to the mix. The mix is agitated gently until a smooth consistency is reached.
The mix is then cast to about 0.05 inch thickness onto a high density polyethylene sheet. The resulting sheet is white and flexible. The resulting density of the sheet is about 0.39 g/cm3. The density of a comparable sheet made with the original non-agglomerated precipitated calcium carbonate is about 0.96 g/cm3. This smokable filler material then is shredded into strips about 1/32 inch wide to provide a smokable cut filler.
An agglomerated matrix filler is provided as follows:
Into about 20 parts tap water at ambient temperature and maintained at high shear in a blender is charged about 5 parts HM Sugarles Pectin, Type LM-20 AS-Z, available from Hercules Chemicals. The mixture is agitated until the pectin is fully hydrated. The mixture Y-119A-R&D:39 is then transferred to an egg beater type mixer.
Separately about 60 parts of precipitated calcium carbonate, as described in Example 1, is added to about 200 parts tap water. To this is added about 0.3 parts polyoxyethylene sorbitan mono-oleate available as Tween 80 from Sigma Chemical Co. is charged into the mixture.
This slurry is then charged into the pectin mixture and agitated for about 15 minutes during which time the mixture foams.
The foamed slurry is cast to about a 0.05 inch thickness onto a high density polyethylene sheet and air dried. After drying the sheet, it is sprayed with a 5 percent aqueous solution of calcium chloride such that the resulting sheet now contains about 1 part calcium chloride. The resulting sheet is white and very brittle.
It is ground and sieved to obtain a -30/+100 US Mesh particle size fraction. The material has a tap density, as measured with a graduated cylinder, of about 0.28 g/cm3. The tap density of the original calcium carbonate, measured by the same method, is about 0.46 g/cm3.
The resulting agglomerated matrix filler is used to manufacture a smokable filler material, in much the same manner as described in Example 1.
Y-119A-R&D:40
Cigarettes of the present invention, when smoked, provide a flavorful mainstream aerosol. The mainstream aerosol of such cigarettes can yield low levels of incomplete combustion products as well as low levels of gas phase components. The cigarettes burn at an acceptable rate, and maintain static smolder, at least Y-119A-R~D:31 when smoked under FTC smoking conditions. The cigarettes, when smoked, have an ash and fire cone which is not overly cohesive, and hence, is not overly long.
However, the cigarettes also provide an ash and fire cone which exhibit good integrity.
Cigarettes of the present invention, when smoked, generally yield less than about 20 mg, preferably less than about 10 mg of sidestream "tar" per cigarette, as determined using the apparatus and techniques described by Proctor et al, Analyst, Vol. 113, p. 1509 (1988).
Such cigarettes normally provide more than about 5 puffs, preferably more than about 6 puffs per cigarette, when smoked under FTC conditions. Normally, cigarettes of the present invention provide less than about 20 puffs, and often less than about 15 puffs, when smoked under FTC
conditions.
The following examples are provided in order to further illustrate the invention but should not be construed as limiting the scope thereof. Unless otherwise noted, all parts and percentages are by weight.
A. Preparation of a Tobacco-Containing Smokable Filler Material A filler is provided as follows:
Into a high shear blender is charged about 500 parts tap water and about 5 parts of a high viscosity ammonium alginate available as Amoloid HV from Kelco Division of Merck & Co., Inc. The resulting mixture is agitated at ambient temperature so as to disperse the alginate in the water and hydrate the alginate. Then, about 95 parts of precipitated calcium carbonate available as USP Light from Pfizer Inc. is added to the water/alginate mixture.
Y-119A-R&D:32 - 20265~9 The resulting slurry is agitated at moderate rate for about 10 minutes until a consistent slurry is provided.
The slurry is spray dried using an Anhydro Type Lab Sl spray dryer having an air atomized nozzle at an inlet temperature of about 290C and an outlet temperature of about 220F. The spray dryer is equipped with a Masterflex Pump System using a Model 7016-20 head supplied by Cole-Parmer Instrument Co. The nozzle air pressure is 4 psi, and the liquid feed rate is that provided by setting the pump speed control to 2. The resulting spray dried particles have a generally spherical shape. The particles are screened to a particle size of -80/+325 U.S. Mesh.
The spray dried particles are free flowing, are essentially insoluble in water at ambient temperature, resist wetting, and remain in an agglomerated state when contacted with water under ambient conditions. The particles each are an agglomerated matrix of a plurality of precipitated calcium carbonate particles spaced within an alginate.
The smokable material is provided as follows:
Into a high shear blender containing 225 parts tap water and set at low speed is charged about 5 parts of a high viscosity ammonium alginate available as Amoloid HV
from Kelco Division of Merck & Co., Inc. The resulting mixture is agitated at ambient temperature so as to disperse the alginate in the water and hydrate the alginate. Then, 20 parts glycerin and 25 parts tap water are charged into the water/alginate mixture. Then, 17.2 parts of the previously described agglomerated calcium carbonate is charged into the mixture. The resulting slurry is agitated until a consistent slurry is provided.
The slurry is cast to about a 0.025 inch thickness onto a high density polyethylene sheet and air dried.
The resulting sheet light brown color and a flexible Y-119A-R&D:33 ~026~39 _ character. The sheet is cut at 32 cuts per inch using a paper shredder.
The shreds of sheet are dusted with about 8.5 parts of finely divided Pennsylvania cigar tobacco laminae.
B. Preparation of a Cigarette Cigarettes substantially as shown in Figure 3 are provided as follows:
The cigarettes each have a length of about 84 mm and a circumference of about 24.8 mm, and include a smokable rod having a length of about 57 mm, a first filter segment having a length of about 15 mm and a second filter segment having a length of about 12 mm. The first and second filter segments form a filter element. Each filter segment is attached to each smokable rod using nonporous tipping paper. For each cigarette, the tipping paper circumscribes the filter element and about a 4 mm length of the smokable rod in the region adjacent the filter element. The filter elements are ventilated to about 60 percent air dilution by providing a ring of perforations through the tipping paper and plug wrap of the filter element circumscribing the cigarette about 12 mm from the extreme mouthend thereof.
The smokable rod includes the previously described tobacco-containing smokable material in cut filler form.
The first filter segment is provided by gathering a 11.75 inch wide web of tobacco and carbon paper available as (P-144-BAC) from Kimberly-Clark Corp. using the filter rod forming apparatus described in Example 1 of U.S.
Patent No. 4,807,809 to Pryor et al. The plug wrap for the filter segment is available as Reference No. 5831 from Ecusta Corp. The first filter segment is positioned adjacent the smokable rod.
Y-119A-R&D:34 The second filter segment is provided by gathering a 11.75 inch wide web of non-woven polypropylene web available as PP-100-F from Kimberly-Clark Corp. using the filter rod forming apparatus described in Example 1 of U.S. Patent No. 4,807,809 to Pryor et al. The plug wrap for the filter segment is available as Reference No. 5831 from Ecusta Corp. The second filter segment is positioned adjacent the first filter segment, at the extreme mouth end of the cigarette.
The cigarette outer paper wrapper exhibits an air permeability of about 0 CORESTA unit. The cigarette paper is available as P-2831-60-1 from Kimberly-Clark Corp.
The inner wrapper of the smokable rod is a tobacco-containing paper available as P-2831-23-3 from Kimberly-Clark Corp.
Smokable cigarette rods are provided using known techniques. In particular, the smokable material is circumscribed by a single layer of paper wrap. The weight of the smokable material within each cigarette rod is about 1 g.
The cigarettes are employed by burning the smokable rod such that the smokable material within the paper wrapper burns to yield smoke. When employed, such cigarettes yield very low levels of visible sidestream smoke and essentially no sidestream odor. The cigarettes do not self-extinguish during the smolder period experienced during FTC smoking conditions.
Particles of calcium carbonate agglomerated with an alginate are provided as follows:
Into a blender is charged about 750 ml tap water, and then about 20 g glycerin. While the mixture is Y-119A-R&D:35 -gently agitated, about 10 g of the ammonium alginate described in Example 1 is slowly added thereto, so as to disperse the alginate in the water. The resulting mixture is transferred into a 1 liter jar, sealed, and gently rolled overnight to hydrate the alginate.
A slurry of 250 g precipitated calcium carbonate available as Code No. 2A from Pfizer Inc. in 250 g tap water is provided. Then, the slurry is added to 200 g of the water/glycerin/alginate mixture. The resulting slurry is agitated gently so as to provide a slurry having a smooth texture.
The slurry is cast onto a high density polyethylene sheet at a thickness of about 0.04 inch, and air dried to provide pieces of dried sheet about 6 inches by about 6 inches in size. The resulting dried sheet is hand ground to a fine particle size and screened to -50 US Mesh.
Particles of calcined agglomerated calcium carbonate are provided as follows:
Into a low shear mixer are charged about 832 parts tap water at ambient temperature, about 757 parts precipitated particulate calcium carbonate available as Albacar 5970 from Pfizer Inc., and about 267 parts molasses. The calcium carbonate has a rosettic structure and an average particle size (i.e., diameter) of about 2 microns. The molasses is available as Refiner's Syrup from Savannah Sugar Co., and has a solids/water content of about 3.7:1. The resulting mixture is agitated for about 5 to about 10 minutes to provide a slurry having a solids content of about 52 percent and a viscosity of about 1,200 cps as measured by a Brookfield LVT
viscometer with cylindrical LV spindle No. 4.
The slurry is spray dried by continuously pumping the slurry at about 6 lbs./min. at a feed pressure of about 475 to about 500 psig to a spray dryer. The spray dryer is a Bowen Type commercial unit equipped with an Y-119A-R&D:36 SD-046 nozzle, and operated in a commercial mode. The inlet temperature is about 470F, and the outlet temperature is about 260F. The resulting spray dried particles have a generally spherical shape, and a moisture content of below about 2 percent. The particles are screened to a particle size of -70/+200 US Mesh.
The spray dried particles are placed on a 12 inch by 36 inch steel tray to a thickness of about 0.5 inch. The tray then is passed into a continuous belt furnace at a rate of about 8 to about 12 inches/min., and is subjected to heating under nitrogen atmosphere at above about 600C
for about 10 minutes, and at above about 400C for about 20 minutes. The oven is set at about 720C, and the tray is subjected to a maximum air temperature of about 670C
during that time. The heated particles are removed from the furnace into a cooling zone for about 1 hour under nitrogen atmosphere, and cooled to ambient temperature.
The calcined particles so collected are black, are spherical in shape, are free flowing, and resist wetting.
The particles are about 93 percent calcium carbonate, and exhibit a bulk density of about 0.5 g/cm3. The particles each are an agglomerated matrix of a plurality of precipitated calcium carbonate particles spaced within a carbonaceous material.
A tobacco-containing smokable filler material is prepared as follows:
Into a high shear blender is charged about 225 ml tap water, and into the water is dispersed about 5 g of the ammonium alginate described in Example 1. The resulting mixture is gently agitated at ambient temperature for about 15 minutes, until the alginate is hydrated. Then, about 20 g glycerin is added to the mixture, followed by about 25 ml tap water. To the mixture is added about 16.7 g of an "American blend" of tobacco cut filler which has been ground to a powder.
Y-119A-R&D:37 Then, about 25 ml tap water is added to the mixture. The resulting mixture is agitated until a smooth slurry results. To the slurry is added a mixture of about 13.8 g of the calcined agglomerated calcium carbonate and about 13.8 g calcium carbonate agglomerated with ammonium alginate. The resulting slurry is agitated until the slurry exhibits a smooth texture. The resulting slurry is cast onto a high density polyethylene sheet at a thickness of about 0.025 inch and air dried.
A. Preparation of an Agglomerated Matrix Filler Into about 500 parts tap water at ambient temperature and maintained at high shear in a blender is charged about 5 parts ammonium alginate available as Amoloid HV. The mixture is agitated until the alginate is fully hydrated. The mixture is then transferred to an egg beater type mixer. Then, about 94.5 parts precipitated calcium carbonate, as described in Example 1, is charged into the mixture. Agitation is continued until the mixture achieves a smooth consistency. Then about 0.5 parts sodium dodecyl sulfate, from Aldrich Chemical Co., is charged into the mix. Agitation is continued for about 15 minutes at which time the mixture foams.
The slurry is cast to about a 0.05 inch thickness onto a high density polyethylene sheet and air dried.
The resulting sheet is white and very brittle. It is ground and sieved to obtain a -30/+lO0 US Mesh particle size fraction. This material does not lose its structure when emersed in water. This is because the binder has become water insoluble. The material has a tap density, as measured with a graduated cylinder, of about Y-119A-R&D:38 0.26 g/cm3. The tap density of the original calcium carbonate, measured by the same method, is about 0.46 g/cm3.
B. Preparation of a Smokable Filler Material Into about 200 parts tap water at ambient temperature and maintained at high shear in a blender is charged about 3.33 parts ammonium alginate as Amoloid HV
and then about 4.5 parts glycerin. The mixture is agitated for about 15 minutes until the components are fully hydrated. The mixture is then transferred to an egg beater type mixer and agitated. Separately, about 60 parts of the above described agglomerated calcium carbonate is mixed with about 400 parts tap water and the resulting slurry is added to the mix. The mix is agitated gently until a smooth consistency is reached.
The mix is then cast to about 0.05 inch thickness onto a high density polyethylene sheet. The resulting sheet is white and flexible. The resulting density of the sheet is about 0.39 g/cm3. The density of a comparable sheet made with the original non-agglomerated precipitated calcium carbonate is about 0.96 g/cm3. This smokable filler material then is shredded into strips about 1/32 inch wide to provide a smokable cut filler.
An agglomerated matrix filler is provided as follows:
Into about 20 parts tap water at ambient temperature and maintained at high shear in a blender is charged about 5 parts HM Sugarles Pectin, Type LM-20 AS-Z, available from Hercules Chemicals. The mixture is agitated until the pectin is fully hydrated. The mixture Y-119A-R&D:39 is then transferred to an egg beater type mixer.
Separately about 60 parts of precipitated calcium carbonate, as described in Example 1, is added to about 200 parts tap water. To this is added about 0.3 parts polyoxyethylene sorbitan mono-oleate available as Tween 80 from Sigma Chemical Co. is charged into the mixture.
This slurry is then charged into the pectin mixture and agitated for about 15 minutes during which time the mixture foams.
The foamed slurry is cast to about a 0.05 inch thickness onto a high density polyethylene sheet and air dried. After drying the sheet, it is sprayed with a 5 percent aqueous solution of calcium chloride such that the resulting sheet now contains about 1 part calcium chloride. The resulting sheet is white and very brittle.
It is ground and sieved to obtain a -30/+100 US Mesh particle size fraction. The material has a tap density, as measured with a graduated cylinder, of about 0.28 g/cm3. The tap density of the original calcium carbonate, measured by the same method, is about 0.46 g/cm3.
The resulting agglomerated matrix filler is used to manufacture a smokable filler material, in much the same manner as described in Example 1.
Y-119A-R&D:40
Claims (36)
1. A cigarette comprising:
(a) smokable filler material having incorporated therein an intimate mixture of (i) agglomerated matrix filler having an inorganic component, and (ii) tobacco; the agglomerated matrix filler being in an agglomerated form having particles of inorganic filler component spaced within a continuous or semi-continuous phase of organic component prior to formation of the intimate mixture; and (b) a wrapping material circumscribing the smokable filler material.
(a) smokable filler material having incorporated therein an intimate mixture of (i) agglomerated matrix filler having an inorganic component, and (ii) tobacco; the agglomerated matrix filler being in an agglomerated form having particles of inorganic filler component spaced within a continuous or semi-continuous phase of organic component prior to formation of the intimate mixture; and (b) a wrapping material circumscribing the smokable filler material.
2. The cigarette of claim 1 wherein the smokable filler material includes a binding agent.
3. The cigarette of claim 2 wherein the binding agent includes ammonium alginate.
4. The cigarette of any one of claims 1, 2, and 3 wherein the tobacco has the form of a tobacco extract.
5. The cigarette of any one of claims 1, 2, and 3 wherein the tobacco has the form of a tobacco extract, further including tobacco cut filler.
6. The cigarette of any one of claims 1, 2, and 3 wherein the tobacco has the form of a tobacco extract wherein the smokable filler material includes an aerosol forming material.
7. The cigarette of claim 1 wherein the wrapping material is a paper having a porosity of less than about 5 CORESTA
units.
units.
8. The cigarette of claim 1 or 7 wherein the agglomerated matrix filler comprises a calcium carbonate component and an alginate component.
9. The cigarette of claim 1 or 7 wherein the agglomerated matrix filler comprises a calcium carbonate component and an alginate component, the cigarette further including tobacco cut filler.
10. The cigarette of claim 1 wherein the agglomerated matrix filler comprises about 10 to about 99 weight parts of a calcium carbonate component for each weight part of organic component.
11. The cigarette of claim 1 further including tobacco cut filler.
12. A cigarette comprising:
(a) smokable filler material having incorporated therein agglomerated matrix filler having an inorganic filler component and an organic component; the agglomerated matrix filler being in an agglomerated form having particles of inorganic filler component spaced within a continuous or semi-continuous phase of organic component prior to formation of the smokable filler material; and (b) a wrapping material circumscribing the smokable filler material.
(a) smokable filler material having incorporated therein agglomerated matrix filler having an inorganic filler component and an organic component; the agglomerated matrix filler being in an agglomerated form having particles of inorganic filler component spaced within a continuous or semi-continuous phase of organic component prior to formation of the smokable filler material; and (b) a wrapping material circumscribing the smokable filler material.
13. The cigarette of claim 12 wherein the smokable filler material includes a binding agent.
14. The cigarette of claim 13 wherein the binding agent includes ammonium alginate.
15. The cigarette of claim 12 wherein the wrapping material is a paper having a porosity of less than about 5 CORESTA
units.
units.
16. The cigarette of claim 12 or 15 wherein the agglomerated matrix filler comprises a calcium carbonate component and an alginate component.
17. The cigarette of claim 12 or 15 wherein the agglomerated matrix filler comprises a calcium carbonate component and an alginate component, the cigarette further including tobacco cut filler.
18. The cigarette of claim 12 wherein the agglomerated matrix filler comprises about 10 to about 99 weight parts of a calcium carbonate component for each weight part of organic component.
19. The cigarette of claim 12 further including tobacco cut filler.
20. A smokable filler material comprising an agglomerated matrix filler material (i) having particles of an inorganic component spaced within a continuous or semi-continuous phase of an organic component, and (ii) being in an agglomerated form prior to formation of the intimate mixture.
21. The smokable filler material of claim 20 including a binding agent.
22. The smokable filler material of claim 21 wherein the binding agent includes an alginate.
23. The smokable filler material of claim 20 or 21 including an aerosol forming material.
24. The smokable filler material of claim 20 or 21 including an aerosol forming material, wherein the aerosol forming material includes glycerin.
25. The smokable filler material of claim 20 or 21 including tobacco.
26. The smokable filler material of claim 20 or 21 including tobacco, wherein the tobacco has the form of an extract.
27. The smokable filler material of claim 20 wherein the inorganic component includes particles of calcium carbonate.
28. The smokable filler material of claims 20 or 27 wherein the organic component includes an alginate.
29. The smokable filler material of claims 20 or 27 wherein the organic component includes an alginate, wherein the material includes diammonium hydrogen orthophosphate.
30. The smokable filler material of claims 20 or 27 wherein the organic component includes an alginate, wherein the material includes residual foaming agent.
31. A cigarette comprising:
(a) smokable filler material having incorporated therein an intimate mixture of (i) agglomerated matrix filler having particles of inorganic component spaced within a continuous or a semi-continuous phase of an organic binding component, the agglomerated matrix filler being essentially insoluble in water at ambient conditions, and (ii) tobacco; the agglomerated matrix filler being in an agglomerated form prior to formation of the intimate mixture; and (b) wrapping material circumscribing the smokable filler material.
(a) smokable filler material having incorporated therein an intimate mixture of (i) agglomerated matrix filler having particles of inorganic component spaced within a continuous or a semi-continuous phase of an organic binding component, the agglomerated matrix filler being essentially insoluble in water at ambient conditions, and (ii) tobacco; the agglomerated matrix filler being in an agglomerated form prior to formation of the intimate mixture; and (b) wrapping material circumscribing the smokable filler material.
32. The cigarette of claim 31 wherein the smokable filler material includes an aerosol forming material.
33. The cigarette of claim 1 or 31 wherein the agglomerated matrix filler comprises a calcium carbonate component and an alginate component.
34. The cigarette of claim 31 wherein the agglomerated matrix filler comprises about 10 to about 99 weight parts of an inorganic component for each weight part of organic component.
35. A cigarette comprising:
(a) smokable filler material having incorporated therein agglomerated matrix filler having particles of inorganic component spaced within a continuous or a semi-continuous phase of an organic binding component, the agglomerated matrix filler being essentially insoluble in water at ambient conditions, the agglomerated matrix filler being in an agglomerated form prior to formation of the smokable filler material; and (b) a wrapping material circumscribing the smokable filler material.
(a) smokable filler material having incorporated therein agglomerated matrix filler having particles of inorganic component spaced within a continuous or a semi-continuous phase of an organic binding component, the agglomerated matrix filler being essentially insoluble in water at ambient conditions, the agglomerated matrix filler being in an agglomerated form prior to formation of the smokable filler material; and (b) a wrapping material circumscribing the smokable filler material.
36. The cigarette of claim 35 wherein the agglomerated matrix filler comprises a calcium carbonate component and an alginate component.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US414,833 | 1989-09-29 | ||
US07/414,833 US5074321A (en) | 1989-09-29 | 1989-09-29 | Cigarette |
US07/567,521 US5129408A (en) | 1990-08-15 | 1990-08-15 | Cigarette and smokable filler material therefor |
US567,521 | 1990-08-15 |
Publications (2)
Publication Number | Publication Date |
---|---|
CA2026539A1 CA2026539A1 (en) | 1991-03-30 |
CA2026539C true CA2026539C (en) | 1995-11-14 |
Family
ID=27022734
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA002026539A Expired - Fee Related CA2026539C (en) | 1989-09-29 | 1990-09-28 | Cigarette and smokable filler material therefor |
Country Status (7)
Country | Link |
---|---|
EP (1) | EP0419975A3 (en) |
JP (1) | JPH03180166A (en) |
KR (1) | KR910005792A (en) |
CN (1) | CN1026751C (en) |
CA (1) | CA2026539C (en) |
HU (1) | HUT57562A (en) |
RU (1) | RU1829919C (en) |
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GB1483461A (en) * | 1974-07-16 | 1977-08-17 | Ici Ltd | Smoking mixtures |
GB2143150B (en) * | 1983-06-15 | 1986-07-30 | British American Tobacco Co | Smoking articles |
-
1990
- 1990-09-15 EP EP19900117780 patent/EP0419975A3/en not_active Withdrawn
- 1990-09-27 JP JP2255490A patent/JPH03180166A/en active Pending
- 1990-09-28 HU HU906262A patent/HUT57562A/en unknown
- 1990-09-28 KR KR1019900015476A patent/KR910005792A/en not_active Withdrawn
- 1990-09-28 CA CA002026539A patent/CA2026539C/en not_active Expired - Fee Related
- 1990-09-28 RU SU904831189A patent/RU1829919C/en active
- 1990-09-29 CN CN90108150A patent/CN1026751C/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
HUT57562A (en) | 1991-12-30 |
RU1829919C (en) | 1993-07-23 |
HU906262D0 (en) | 1991-03-28 |
CN1050491A (en) | 1991-04-10 |
KR910005792A (en) | 1991-04-27 |
CA2026539A1 (en) | 1991-03-30 |
EP0419975A3 (en) | 1991-08-07 |
EP0419975A2 (en) | 1991-04-03 |
CN1026751C (en) | 1994-11-30 |
JPH03180166A (en) | 1991-08-06 |
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