US3524452A - Process for increasing the filling capacity of tobacco - Google Patents
Process for increasing the filling capacity of tobacco Download PDFInfo
- Publication number
- US3524452A US3524452A US720068A US72006868A US3524452A US 3524452 A US3524452 A US 3524452A US 720068 A US720068 A US 720068A US 72006868 A US72006868 A US 72006868A US 3524452 A US3524452 A US 3524452A
- Authority
- US
- United States
- Prior art keywords
- tobacco
- water
- liquid
- parts
- freon
- 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 - Lifetime
Links
- 241000208125 Nicotiana Species 0.000 title description 207
- 235000002637 Nicotiana tabacum Nutrition 0.000 title description 207
- 238000000034 method Methods 0.000 title description 33
- 238000011049 filling Methods 0.000 title description 30
- 239000007788 liquid Substances 0.000 description 114
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 94
- 239000007789 gas Substances 0.000 description 77
- CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 description 52
- 239000000945 filler Substances 0.000 description 21
- 239000000203 mixture Chemical class 0.000 description 19
- 238000005470 impregnation Methods 0.000 description 18
- 238000010438 heat treatment Methods 0.000 description 14
- 239000003570 air Substances 0.000 description 13
- 235000019504 cigarettes Nutrition 0.000 description 12
- 239000007921 spray Substances 0.000 description 12
- 238000009835 boiling Methods 0.000 description 11
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
- 239000002245 particle Substances 0.000 description 5
- 239000000796 flavoring agent Substances 0.000 description 4
- 235000019634 flavors Nutrition 0.000 description 4
- 229910052736 halogen Inorganic materials 0.000 description 4
- 125000005843 halogen group Chemical group 0.000 description 4
- 238000011084 recovery Methods 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- -1 alkanols Chemical group 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 150000005826 halohydrocarbons Chemical class 0.000 description 3
- 229930195733 hydrocarbon Natural products 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 3
- 238000003860 storage Methods 0.000 description 3
- 235000019505 tobacco product Nutrition 0.000 description 3
- SYBYTAAJFKOIEJ-UHFFFAOYSA-N 3-Methylbutan-2-one Chemical compound CC(C)C(C)=O SYBYTAAJFKOIEJ-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- RGSFGYAAUTVSQA-UHFFFAOYSA-N Cyclopentane Chemical compound C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 2
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 150000001338 aliphatic hydrocarbons Chemical group 0.000 description 2
- XXROGKLTLUQVRX-UHFFFAOYSA-N allyl alcohol Chemical compound OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 description 2
- BTANRVKWQNVYAZ-UHFFFAOYSA-N butan-2-ol Chemical compound CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 description 2
- 235000019506 cigar Nutrition 0.000 description 2
- HGCIXCUEYOPUTN-UHFFFAOYSA-N cyclohexene Chemical compound C1CCC=CC1 HGCIXCUEYOPUTN-UHFFFAOYSA-N 0.000 description 2
- 230000001419 dependent effect Effects 0.000 description 2
- 239000008246 gaseous mixture Substances 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- FDPIMTJIUBPUKL-UHFFFAOYSA-N pentan-3-one Chemical compound CCC(=O)CC FDPIMTJIUBPUKL-UHFFFAOYSA-N 0.000 description 2
- 238000002791 soaking Methods 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- 229940029284 trichlorofluoromethane Drugs 0.000 description 2
- 230000008016 vaporization Effects 0.000 description 2
- SLGOCMATMKJJCE-UHFFFAOYSA-N 1,1,1,2-tetrachloro-2,2-difluoroethane Chemical compound FC(F)(Cl)C(Cl)(Cl)Cl SLGOCMATMKJJCE-UHFFFAOYSA-N 0.000 description 1
- BOSAWIQFTJIYIS-UHFFFAOYSA-N 1,1,1-trichloro-2,2,2-trifluoroethane Chemical compound FC(F)(F)C(Cl)(Cl)Cl BOSAWIQFTJIYIS-UHFFFAOYSA-N 0.000 description 1
- SCYULBFZEHDVBN-UHFFFAOYSA-N 1,1-Dichloroethane Chemical compound CC(Cl)Cl SCYULBFZEHDVBN-UHFFFAOYSA-N 0.000 description 1
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 1
- DDMOUSALMHHKOS-UHFFFAOYSA-N 1,2-dichloro-1,1,2,2-tetrafluoroethane Chemical compound FC(F)(Cl)C(F)(F)Cl DDMOUSALMHHKOS-UHFFFAOYSA-N 0.000 description 1
- MPPPKRYCTPRNTB-UHFFFAOYSA-N 1-bromobutane Chemical compound CCCCBr MPPPKRYCTPRNTB-UHFFFAOYSA-N 0.000 description 1
- PZHIWRCQKBBTOW-UHFFFAOYSA-N 1-ethoxybutane Chemical compound CCCCOCC PZHIWRCQKBBTOW-UHFFFAOYSA-N 0.000 description 1
- CXBDYQVECUFKRK-UHFFFAOYSA-N 1-methoxybutane Chemical compound CCCCOC CXBDYQVECUFKRK-UHFFFAOYSA-N 0.000 description 1
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 1
- PITMOJXAHYPVLG-UHFFFAOYSA-N 2-acetyloxybenzoic acid;n-(4-ethoxyphenyl)acetamide;1,3,7-trimethylpurine-2,6-dione Chemical compound CCOC1=CC=C(NC(C)=O)C=C1.CC(=O)OC1=CC=CC=C1C(O)=O.CN1C(=O)N(C)C(=O)C2=C1N=CN2C PITMOJXAHYPVLG-UHFFFAOYSA-N 0.000 description 1
- BSPCSKHALVHRSR-UHFFFAOYSA-N 2-chlorobutane Chemical compound CCC(C)Cl BSPCSKHALVHRSR-UHFFFAOYSA-N 0.000 description 1
- MSXVEPNJUHWQHW-UHFFFAOYSA-N 2-methylbutan-2-ol Chemical compound CCC(C)(C)O MSXVEPNJUHWQHW-UHFFFAOYSA-N 0.000 description 1
- VOPWNXZWBYDODV-UHFFFAOYSA-N Chlorodifluoromethane Chemical compound FC(F)Cl VOPWNXZWBYDODV-UHFFFAOYSA-N 0.000 description 1
- PMPVIKIVABFJJI-UHFFFAOYSA-N Cyclobutane Chemical compound C1CCC1 PMPVIKIVABFJJI-UHFFFAOYSA-N 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- QSJXEFYPDANLFS-UHFFFAOYSA-N Diacetyl Chemical group CC(=O)C(C)=O QSJXEFYPDANLFS-UHFFFAOYSA-N 0.000 description 1
- 239000004338 Dichlorodifluoromethane Substances 0.000 description 1
- ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 1
- XOBKSJJDNFUZPF-UHFFFAOYSA-N Methoxyethane Chemical compound CCOC XOBKSJJDNFUZPF-UHFFFAOYSA-N 0.000 description 1
- 239000004341 Octafluorocyclobutane Substances 0.000 description 1
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical group ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 1
- 238000007605 air drying Methods 0.000 description 1
- 150000001350 alkyl halides Chemical class 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical group 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- RJCQBQGAPKAMLL-UHFFFAOYSA-N bromotrifluoromethane Chemical compound FC(F)(F)Br RJCQBQGAPKAMLL-UHFFFAOYSA-N 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- HRYZWHHZPQKTII-UHFFFAOYSA-N chloroethane Chemical compound CCCl HRYZWHHZPQKTII-UHFFFAOYSA-N 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 238000010908 decantation Methods 0.000 description 1
- 230000006735 deficit Effects 0.000 description 1
- 230000032798 delamination Effects 0.000 description 1
- FJBFPHVGVWTDIP-UHFFFAOYSA-N dibromomethane Chemical compound BrCBr FJBFPHVGVWTDIP-UHFFFAOYSA-N 0.000 description 1
- PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 description 1
- 235000019404 dichlorodifluoromethane Nutrition 0.000 description 1
- 229940087091 dichlorotetrafluoroethane Drugs 0.000 description 1
- POLCUAVZOMRGSN-UHFFFAOYSA-N dipropyl ether Chemical compound CCCOCCC POLCUAVZOMRGSN-UHFFFAOYSA-N 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000011067 equilibration Methods 0.000 description 1
- 150000002170 ethers Chemical group 0.000 description 1
- 229960003750 ethyl chloride Drugs 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- DMEGYFMYUHOHGS-UHFFFAOYSA-N heptamethylene Natural products C1CCCCCC1 DMEGYFMYUHOHGS-UHFFFAOYSA-N 0.000 description 1
- QTBFPMKWQKYFLR-UHFFFAOYSA-N isobutyl chloride Chemical compound CC(C)CCl QTBFPMKWQKYFLR-UHFFFAOYSA-N 0.000 description 1
- ULYZAYCEDJDHCC-UHFFFAOYSA-N isopropyl chloride Chemical compound CC(C)Cl ULYZAYCEDJDHCC-UHFFFAOYSA-N 0.000 description 1
- 150000002576 ketones Chemical group 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- PYLWMHQQBFSUBP-UHFFFAOYSA-N monofluorobenzene Chemical compound FC1=CC=CC=C1 PYLWMHQQBFSUBP-UHFFFAOYSA-N 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- SNMVRZFUUCLYTO-UHFFFAOYSA-N n-propyl chloride Chemical compound CCCCl SNMVRZFUUCLYTO-UHFFFAOYSA-N 0.000 description 1
- 239000008239 natural water Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- BCCOBQSFUDVTJQ-UHFFFAOYSA-N octafluorocyclobutane Chemical compound FC1(F)C(F)(F)C(F)(F)C1(F)F BCCOBQSFUDVTJQ-UHFFFAOYSA-N 0.000 description 1
- 235000019407 octafluorocyclobutane Nutrition 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 230000001007 puffing effect Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 230000000391 smoking effect Effects 0.000 description 1
- 239000002195 soluble material Substances 0.000 description 1
- 238000004326 stimulated echo acquisition mode for imaging Methods 0.000 description 1
- 239000008399 tap water Substances 0.000 description 1
- 235000020679 tap water Nutrition 0.000 description 1
- RKSOPLXZQNSWAS-UHFFFAOYSA-N tert-butyl bromide Chemical compound CC(C)(C)Br RKSOPLXZQNSWAS-UHFFFAOYSA-N 0.000 description 1
- NBRKLOOSMBRFMH-UHFFFAOYSA-N tert-butyl chloride Chemical compound CC(C)(C)Cl NBRKLOOSMBRFMH-UHFFFAOYSA-N 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- KFUSEUYYWQURPO-OWOJBTEDSA-N trans-1,2-dichloroethene Chemical compound Cl\C=C\Cl KFUSEUYYWQURPO-OWOJBTEDSA-N 0.000 description 1
- UBOXGVDOUJQMTN-UHFFFAOYSA-N trichloroethylene Natural products ClCC(Cl)Cl UBOXGVDOUJQMTN-UHFFFAOYSA-N 0.000 description 1
- 229930195735 unsaturated hydrocarbon Natural products 0.000 description 1
- 238000009834 vaporization Methods 0.000 description 1
- 210000003462 vein Anatomy 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
Images
Classifications
-
- A—HUMAN NECESSITIES
- A24—TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
- A24B—MANUFACTURE OR PREPARATION OF TOBACCO FOR SMOKING OR CHEWING; TOBACCO; SNUFF
- A24B3/00—Preparing tobacco in the factory
- A24B3/18—Other treatment of leaves, e.g. puffing, crimpling, cleaning
- A24B3/182—Puffing
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S131/00—Tobacco
- Y10S131/902—Inorganic chemical agents employed in puffing tobacco
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S131/00—Tobacco
- Y10S131/903—Fixing the product after puffing
Definitions
- the filling capacity stream of tobacco is in-' creased by adjusting the moisture content of tobacco, wetting the tobacco with an inert organic liquid and rapidly vaporizing the liquid from the tobacco by passing the stream of tobacco into contact with a rapidly moving stream of gas heated to a temperature substantially above the boiling point of the organic liquid.
- the tobacco expansion occurs in the disclosed technique in a period ofless than about 4 seconds.
- Tobacco leaves when harvested, contain a considerable quantity of water and during the tobacco curing process this water is removed by drying resulting in shrinkage of the leaf structure.
- the tobacco regains very little, if any, of the shrinkage resulting from drying so that a significant loss in the filling capacity of the tobacco is the result.
- the tobacco has a bulk density which is in excess of that necessarily required for making satisfactory cigars or cigarettes.
- frequently shreds are laminiated together to form dense hard particles which occupy far less volume than the original shreds would occupy. This is, of course, wasteful.
- a further object of the invention is to provide a process for significantly increasing the filling capacity of tobacco which process can be efficiently conducted while maintaining processing costs at a minimum.
- a still further object of the present invention is to provide a process for increasing the filling capacity of tobacco which process can be conducted in a continuous manner using readily available equipment.
- a moist, cured tobacco having a water content in the range of about 10 to 100 parts of water per 100 parts of tobacco is employed.
- the water content of the tobacco is within the range of 13 to 50 parts per 100 parts of tobacco and most preferably within the range of 18 to 30 parts per .100 parts of tobacco.
- 100 parts of tobacco means tobacco on a water-free basis.
- a cured tobacco having a natural water content of 12.3% is described herein as having about 14.] parts of water per 100 parts of tobacco.
- the lower moisture limit of the tobacco to be treated is for the main imposed by the fragility of the tobacco; tobacco which is too dry tends to disintegrate and to produce fines.
- the amount of water employed can be large enough to permit the tobacco to be soaking wet; however, the use of water in amounts such that the tobacco is very wet is preferably avoided because of mechanical difficulties in handling such wet masses of tobacco.
- the upper limit of 100 parts of moisture per 100 parts of tobacco is a practical preferred operating limit.
- the moistening operation can be carried out at ambient temperatures and also at elevated temperatures. It is usually preferred to maintain the tobacco below about 170 F. in order to avoid impairing flavor. In general, the moistening is carried out at ambient atmospheric temperatures such as 60 F. to F.
- the water can be added to the tobacco by any technique which results in a substantially uniform moistened mass, such as by spraying or soaking.
- the tobacco is then contacted with sufficient quantity of a volatile organic liquid for a time sufficient to accomplish thorough impregnation of the tobacco.
- the impregnation can be carried out at any suitable temperature but preferably is carried out at a temperature below about 170 F. in order to avoid impairing the flavor of the tobacco. It has been observed that the time needed to impregnate substantially uniformly the mass of tobacco is temperature dependent; also the time of impregnation is dependent upon the particle size of the tobacco. The larger the particle size the longer the time.
- the illustrative times for strips and shreds are: F., 0.5 to 1 hour; 100 F., 12-24 hours; 75 F., 40-100 hours.
- the or ganic liquid is one having a boiling point below that of water.
- lt is thought that in addition to helping to expand tobacco structure the inert organic liquid helps to set the cells in expanded condition.
- the organic liquid should not be one which does combine irreversibly to a significant degree with the tobacco; in other words it must not alter the smoking qualities of the product to an undesirable extent, i.e., it should be chemically inert.
- the liquid falls into the classes of aliphatic hydrocarbons, aromatic hydrocarbons, alkanols, ketones, aliphatic esters, ethers, halogen substituted hydrocarbons and mixtures thereof. It is preferred to operate with the lower boiling members of these classes. lt is intended that lower boiling include those liquids having a boiling point below about 231 F. (1l0.7 C.) and preferably below about F. (68.5 C.).
- Illustrative suitable inert organic liquids are: benzene and toluene; acetone, methyl ethyl ketone, methyl isopropyl ketone, diethyl ketone and diacetyl; methyl ethyl ether, diethyl ether, dipropyl ether, diisopropyl ether, methyl butyl ether, ethyl butyl ether, ethylene glycol dimethyl ether, and tetrahydrofuran; methanol, ethanol, propanol, isopropanol, sec-butyl alcohol, t-butyl alcohol, t-amyl alcohol, and allyl alcohol; butane, pentane, hexane, heptane, and the corresponding unsaturated hydrocarbons; and cyclobutane, cyclopentane, cyclohexane and cyclohexene.
- the halogen substituted hydrocarbons may be aliphatic, cycloaliphatic or aromatic in nature. One or more halogen atoms may be present in each halohydrocarbon molecule. Two or more different halogens may be present in a single halohydrocarbon molecule.
- lllustrative halohydrocarbons are ethyl chloride, propyl chloride, isopropyl chloride, vinylidene chloride, n-butyl bromide, isobutyl chloride, sec-butyl chloride, t-butyl chloride, t-butyl bromide, methylene chloride, methylene bromide, chloroform, carbon tetrachloride, ethylene dichloride, ethylidene chloride,
- inert organic liquids are aliphatic hydrocarbons having 3 to 6 carbon atoms and the halogen substituted alkane hydrocarbons (halo-alkane) having l-2 carbon atoms and the halocycloalkanes having 3-4 carbon atoms.
- Those compounds generally known as Freon fluorocarbons are especially preferred.
- lllustrative of the preferred Freon liquids are trichloromonofluoromethane, dichlorodifluoromethane, monobromotrifluoromethane, monochlorodifluoromethane, dichlorotetrafluoroethane, tetrachlorodifluoroethane.
- the amount of impregnating inert organic liquid is controlled for optimum results; broadly speaking it is between 15 parts of liquid per 100 parts of tobacco and about the maximum impregnation amount of liquid.
- the maximum impregnation amount is the maximum amount which can be taken up by the tobacco.
- the amount of impregnating liquid used is between about 25 parts and about 350 parts per 100 parts of tobacco.
- the temperature and pressure conditions under which the tobacco is contacted with the organic liquid are not critical, and generally speaking, ordinary room temperatures and pressures are entirely satisfactory. No special equipment is required for impregnating the tobacco with the inert organic liquid and impregnation can be carried out in any suitable type of tank, drum or other container. However, in the case of liquids having a low boiling point or high vapor pressure, the impregnation should be carried out at reduced temperatures or elevated pressures so that the liquid does not vaporize during the equilibration step.
- the organic liquid is rapidly removed therefrom. This is accomplished by passing a hot gas through the impregnated tobacco to rapidly remove the organic liquid in a short period, such as on the order of a few seconds, as for example a period of less than about 4 seconds. in order to obtain the desired volume increase of tobacco and avoid impairing flavor quality, it is particularly advantageous to remove the organic impregnating liquid rapidly.
- Use of hot gas at a temperature of between 250 F. and 400 F. effectively removes the impregnating liquid very rapidly so as to cause expansion of the tobacco structure while avoiding shattering the tobacco into dust or fines.
- the expansion of the structure also causes delamination of laminated shreds which serves to increase the filling capacity and also improves the burning qualities of the filler.
- the organic liquid removal is preferably carried out at substantially atmospheric pressure but it can be carried out at super-atmospheric pressures when using very low boiling liquid.
- the gas is employed at a temperature at least about 200 F. higher than the boiling point of the organic liquid employed for impregnation. The temperature of the gas thus depends on the boiling point of the organic impregnating liquid. It is preferred to avoid use of gas temperatures higher than about 400 F. so as to avoid flavor impairment of the tobacco composition.
- the gas is preferably maintained at a temperature below about 350 F.
- the hot gas is preferably a mixture of vaporized organic liquid and steam, but other hot gases such as, for example, air, nitrogen, carbon dioxide, gaseous organic liquid or mixtures thereof or any other gas which is inert with respect to the tobacco and the volatile organic impregnating liquid can be advantageously employed.
- the organic liquid can be recovered, condensed and recycled for further use.
- the expanded tobacco is then reordered to the water content desired for the particular end use. By reordering it is meant that the moisture content ofthe expanded tobacco is adjusted to a desired value such as, for example, 12-13% for cut filler for cigarette makmg.
- Tobacco moistener l is a unit adapted for adding water from line 2 to cured tobacco feed from line 3.
- Moistener 1 may add the water by means of spraying, or passage through a pool of water with provisions made for draining off excess water and for a period of time during which the water diffuses throughout the mass of tobacco. ln order to maintain the water soluble components in the tobacco, any water which is drained from the moist tobacco is recycled by way of line 2, thus preventing net extraction of soluble material from the tobacco. In some instances the tobacco may already have a moisture content equal to the desired water content of the moist tobacco.
- moistener 1 would be bypassed (by way ofline 3A
- the moist tobacco is passed by way of conveyor line 4 to impregnator 6 which can, for example, be a closed cylinder provided with a screw for moving the moist tobacco therethrough.
- impregnator 6 which can, for example, be a closed cylinder provided with a screw for moving the moist tobacco therethrough.
- the moist tobacco is impregnated with organic liquid from line 7.
- the organic liquid can be added in much the same manner as is the water in moistener 1.
- any drained liquid from impregnator 6 is recycled (via line 7A) to line 7 in order to reduce losses of liquid soluble components from the tobacco.
- lmpregnator 6 is adapted to operate at moderately elevated temperatures such as F usually at autogenous pressure.
- lmposed pressures can be used to help maintain the organic liquid in the liquid state and to increase the impregnation rate.
- 700 pounds of cut filler tobacco, pounds of water and 1200 pounds of Freon 11 can be introduced into impregnator 6 with the tobacco remaining in the impregnator for approximately 30 minutes.
- the moist, impregnated tobacco is then passed by way of line 8 to line 9 for introduction into tobacco expander 13.
- a gaseous mixture such as Freon and steam is passed from gas heater 11 by way of line 9 into expander 13 where the hot gas and the moist impregnated tobacco are thoroughly intermingled.
- Fan 12 is employed for flowing the hot gas through expander 13. lllustratively, when expanding 700 pounds of moist, impregnated tobacco per hour a gaseous mixture of 280,000 pounds of Freon 11 and 38,700 pounds of steam per hour are introduced into expander 13 at a temperature of about 340 F. and a linear velocity of approximately 27 feet per second. With an expander unit of 84 feet in height, the moist impregnated tobacco is contacted with the hot gas for approximately 3.1 seconds.
- the tobacco is expanded (increased in filling capacity) with the hot gas carrying the expanded tobacco into separator 14.
- Separator 14 can be any conventional form of separator such as a cyclone type.
- the expanded tobacco product is withdrawn from separator 14 by way of line 16 and passed, if desired, for processing economy, into a residual liquid removal operation in unit 17.
- the expanded tobacco is contacted with steam introduced through line 18 in an amount sufficient to vaporize all of the residual organic liquid.
- the condensed steam from residual removal operation 17 is passed by way of line 19 to a recovery operation for recovery of the organic liquid content.
- the organic liquid-free tobacco from residual liquid removal operation 17 is reordered to a water content suitable for storage or immediate use. If reordering is desired, the liquid-free tobacco is passed to reordering operation 21 where it is brought to the desired moisture content by drying or moistening operations well known to the tobacco industry. The reordered expanded tobacco composition (product) is then passed to storage for subsequent use through line 22.
- the heating gas and organic liquid vapor and water vapor removed from the moist impregnated tobacco are recycled from separator 14 via line 28 to gas heater 11, thence to expander 13 via line 9. Excess gases from the recycle circuit are bled by way of line 23 into liquid recovery operation 24. Here the water and liquid are condensed. Water is removed by way of line 26 and organic liquid is recycled to impregnator 6 by way of line 27. Where organic liquid immiscible with water is employed, simple decantation is used for separation. Distillation is used for recovery of organic liquids which are miscible with water.
- the moist tobacco was dipped in F reon-MF liquid utilizing a total of 8 liters of the liquid (300 parts of Freon-MF per 100 parts of tobacco).
- the tobacco was sealed in a pressure vessel, which was then heated 75 minutes by water at 133 F internal pressure was 30 pounds per square inch, gauge, at the end of the heating period.
- the vessel was then cooled by water at 50 F. for minutes, and 2650 milliliters of excess liquid Freon-MF was drained from the vessel affording a net impregnation of 201 parts of F reon-MF per 100 parts of tobacco.
- the tobacco was then intimately contacted in a vertical column with a hot gas mixture, comprising air, water vapor, and gaseous Freon-MF, at a gas inlet temperature of 330 F. for a contact time of about 2 seconds.
- a hot gas mixture comprising air, water vapor, and gaseous Freon-MF, at a gas inlet temperature of 330 F. for a contact time of about 2 seconds.
- Tobacco from the hot gas contacting was reordered with a water spray and bulked overnight (allowed to stand in a closed vessel overnight to equilibrate the moisture).
- the vessel was then cooled by water at 50 F. for minutes, and 3150 milliliters of excess liquid Freon-MF was drained from the vessel providing a net impregnation of 182 parts of Freon-MF per 100 parts of tobacco.
- the tobacco was then intimately contacted in a vertical column with a hot gas mixture, comprising air, water vapor, and Freon-MF gas, at a gas inlet temperature of 330 F. for a contact time of about 1 second.
- Tobacco feed rate was uniform over a period of 20 minutes. Tobacco from the hot gas contacting was reordered with'a water spray and bulked overnight.
- Flue-cured cut filler 5700 grams containing 11.3% moisture, was sprayed with 570 milliliters of water and bulked 25 one hour (24 parts water per 100 parts of tobacco).
- the moist tobacco was dipped in Freon-MF liquid comprising that drained from a previous run, using a total of 12 liters of the liquid (350 parts Freon-MF per 100 parts of tobacco).
- the tobacco was sealed ina pressure vessel, which was then heated for 90 minutes by water at 134 F.; internal pressure was 37 pounds per square inch, gauge, at the end of the heating period. The vessel was then cooled by water at F.
- Treated product 5 0 EXAMPLE 5 Burley cut filler 3920 grams containing 11.6% moisture, was sprayed with 392 milliliters of water and bulked overnight (24.4 parts of water per 100 parts of tobacco).
- the moist tobacco was dipped in Freon-MF liquid comprising that drained from a previous run, using a total of 7 liters of the I liquid.
- the tobacco was sealed in a pressure vessel, which was then heated for 90 minutes by water at 127 F internal pressure was 26 pounds per square inch, gauge, at the end of the heating period. The vessel was then cooled by water at 50 F.
- Tobacco feed rate was uniform over a period of 7 minutes. Tobacco from the hot gas contacting was reordered with a water spray and bulked overnight.
- the tobacco was then intimately contacted by passing it through a vertical column with a hot gas mixture, comprising air, water vapor, and Freon-MF gas, at a gas inlet temperature of 347 F. for a contact time of about 0.7 seconds.
- a hot gas mixture comprising air, water vapor, and Freon-MF gas
- the tobacco feed rate was uniform over a period of 16 minutes.
- Tobacco from the hot gas contacting was reordered with a water spray and bulked overnight.
- the impregnated tobacco was then intimately contacted by passing it through a vertical column with a hot gas mixture, comprising air, water vapor, and Freon-MF gas, at a gas inlet temperature of 347 F. for a contact time of about 0.7 seconds.
- a hot gas mixture comprising air, water vapor, and Freon-MF gas
- the tobacco feed rate was uniform over a period of 13 minutes.
- Tobacco from the hot gas contacting was reordered with a water spray and bulked overnight.
- the impregnated tobacco was then intimately contacted by passing it through a vertical column with a hot gas mixture, comprising air, water vapor, and Freon-MF gas, at a gas inlet temperature of 347 F. for a contact time of the tobacco with the hot gases ofabout 0.7 seconds.
- the tobacco feed rate was uniform over a period of 12 l/4 minutes. Tobacco from the hot gas contacting was cooled and reordered with a water spray, and bulked overnight.
- Flue-cured cut filler 5700 grams containing 17.3% moisture, was placed in a pressure vessel, and 10 liters of Freon-MF liquid, comprising that drained from a previous run, was poured over the tobacco (313 parts Freon-MF per parts of tobacco).
- the vessel was sealed and heated for one hour by water at 147 F.; internal pressure was 40 pounds per square inch, gauge, at the end of the heating period.
- the vessel was then cooled by water at 50 F. for 16 minutes, and 4000 milliliters of excess liquid Freon-MF was drained from the vessel giving a net impregnation of 188 parts of Freon-MF per 100 parts of tobacco.
- the liquid-impregnated tobacco was then intimately contacted by passing it through a vertical column with a hot gas mixture, comprising air, water vapor, and Freon-MF gas, at a gas inlet temperature of 343 F. for a contact time of about 0.65 seconds.
- a hot gas mixture comprising air, water vapor, and Freon-MF gas
- the tobacco feed rate was uniform over a period of 12 3/4 minutes.
- Tobacco from the hot gas contacting was cooled, and reordered with a water spray, and bulked overnight.
- Flue-cured cut filler 5700 grams containing 17.6% moisture, was placed in a pressure vessel and 8 liters of Freon- MF liquid, comprising that drained from a previous run, was poured over the tobacco, and 2000 milliliters of excess liquid Freon-MF was drained from the vessel.
- the vessel was then sealed and heated for one hour by water at 151 F.; internal Control 11. 3 463 pressure was 31 pounds per square inch, gauge, at the end of the heating period.
- the vessel was then cooled by water at 50 F. for 6 minutes, and 1500 milliliters more excess liquid Freon-MF was drained from the vessel.
- the tobacco was then intimately contacted by passing it through a vertical column with a flowing hot gas mixture, comprising air, water vapor, and Freon-MF gas, at a gas inlet temperature of 339 F. for a contact time of tobacco with hot gas of about 0.65 seconds.
- the tobacco feed rate was uniform over a period of 10 minutes. Tobacco from the hot gas contacting was reordered with a water spray and bulked overnight.
- the treated tobacco was then intimately contacted with a flowing hot gas mixture, comprising air, water vapor, isopropanol vapor, and Freon-MF gas.
- a flowing hot gas mixture comprising air, water vapor, isopropanol vapor, and Freon-MF gas.
- Tobacco from the hot gas contacting was reordered with a water spray and bulked overnight.
- the process of the present invention can be applied to cured tobacco in the form of leaf (including veins and stems), strips (leaf with stems removed) or cut filler (strips shredded for cigarette making).
- leaf or strips the types or grades of tobacco can be selected for which the process is most effective, thereby achieving results near the maximum while holding processing costs to a minimum.
- stems are preferred rather than leaf, and in any event stems can be processed separately. If the entire blend is to be treated, then cut filler is preferably utilized.
- a process of increasing the filling capacity of tobacco which comprises providing a stream of tobacco moistened with a volatile organic liquid, flowing said moistened tobacco stream into a rapidly moving stream of a gas heated to a temperature substantially above the boiling point of the organic liquid at the prevailing pressure whereby the liquid is rapidly volatilized and the tobacco is expanded in a period of less than about 4 seconds, and separating the expanded tobacco from the hot gas and volatized liquid stream.
- a process of increasing the filling capacity of tobacco which comprises contacting tobacco having a moisture content of between 10 and 100 parts of water per 100 parts of tobacco (dry basis) with a volatile organic liquid in an amount to impregnate the moist tobacco with said liquid, suspending the moist tobacco impregnated with said organic liquid in a stream of rapidly moving gas heated to a temperature substantially above the boiling point of the organic liquid at the prevailing pressure whereby the organic liquid is rapidly vaporized within the tobacco and the tobacco is expanded in a period of less than about 4 seconds, and then separating the tobacco from the gas stream containing vapors of said organic liquid.
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- Manufacture Of Tobacco Products (AREA)
Description
United States Patent Inventors Glenn Philip Moser Winston-Salem, North Carolina; Grant Mathews Stewart, Winston-Salem, North Carolina Appl. No. 720,068
Filed April 10, 1968 Patented Aug. 18, 1970 Assignee RJ. Reynolds Tobacco Company Winston-Salem, North Carolina a Corp. of New Jersey PROCESS FOR INCREASING THE FILLING A.P.C. application of Boehme et a1., Ser. No. 304,214, published May 11, 1943.
Primary Examiner-Melvin D. Rein Attorney- Pendleton, Neuman, Williams and Anderson ABSTRACT: The filling capacity stream of tobacco is in-' creased by adjusting the moisture content of tobacco, wetting the tobacco with an inert organic liquid and rapidly vaporizing the liquid from the tobacco by passing the stream of tobacco into contact with a rapidly moving stream of gas heated to a temperature substantially above the boiling point of the organic liquid. The tobacco expansion occurs in the disclosed technique in a period ofless than about 4 seconds.
26 3 WATER i? 6115 RCOVERY SEPARATOR E x p TOBACCO PRODUCT LIQUID 6 REORDERING RESIDUAL L r EREMOVAL g F- 3 I?) L R WATER 27 -28 ORGAN/C LIQUID 7 STEAM a 13 7A 4 {I 2 I IMPREGNATOR 1 WATER 3 6) TOBACCO gge g MOISTENER GAS HEATER PROCESS FOR INCREASING THE FILLING CAPACITY OF TOBACCO This invention relates to a process for treating tobacco to increase its filling capacity.
Tobacco leaves, when harvested, contain a considerable quantity of water and during the tobacco curing process this water is removed by drying resulting in shrinkage of the leaf structure. In the usual process of preparing tobacco for storage and subsequent cigar and cigarette manufacture, the tobacco regains very little, if any, of the shrinkage resulting from drying so that a significant loss in the filling capacity of the tobacco is the result. Thus, the tobacco has a bulk density which is in excess of that necessarily required for making satisfactory cigars or cigarettes. Also, in the cutting of strips for making cut filler for cigarettes, frequently shreds are laminiated together to form dense hard particles which occupy far less volume than the original shreds would occupy. This is, of course, wasteful.
Several procedures have been suggested in the prior art for increasing the normal filling capacity of dried or cured tobacco. Certain of these processes involve puffing operations in which tobacco is subjected to high pressure steam followed by sudden release of the pressure. Also, it has been suggested that the filling capacity of tobacco may be increased, i.e., bulk density reduced, by exposing the tobacco particles to the vapors of an organic liquid or to an organic liquid followed by air drying at ordinary temperatures. However, these prior procedures have not been wholly satisfactory because (a) they are not effective for expanding the filling capacity to any great extent or (b) they result in a shattering of the tobacco particles so that considerable waste incident to the formation of fines results.
The copending application of James Donald Fredrickson, Serial No. 720,406 filed April 10,1968, discloses and claims a process for increasing the filling capacity of tobacco by moistening tobacco with a volatile organic liquid and then heating the moistened tobacco by means of a hot gas to volatilize the liquid and expand the tobacco. The present invention affords improvements on the Fredrickson process. Thus, it is a principal object of the present invention to provide a process for significantly and consistently increasing the filling capacity of tobacco in convenient manner.
A further object of the invention is to provide a process for significantly increasing the filling capacity of tobacco which process can be efficiently conducted while maintaining processing costs at a minimum.
A still further object of the present invention is to provide a process for increasing the filling capacity of tobacco which process can be conducted in a continuous manner using readily available equipment.
ln accordance with this invention, a moist, cured tobacco having a water content in the range of about 10 to 100 parts of water per 100 parts of tobacco is employed. Preferably, the water content of the tobacco is within the range of 13 to 50 parts per 100 parts of tobacco and most preferably within the range of 18 to 30 parts per .100 parts of tobacco. The term 100 parts of tobacco means tobacco on a water-free basis. To illustrate, a cured tobacco having a natural water content of 12.3% is described herein as having about 14.] parts of water per 100 parts of tobacco. The lower moisture limit of the tobacco to be treated is for the main imposed by the fragility of the tobacco; tobacco which is too dry tends to disintegrate and to produce fines. The amount of water employed can be large enough to permit the tobacco to be soaking wet; however, the use of water in amounts such that the tobacco is very wet is preferably avoided because of mechanical difficulties in handling such wet masses of tobacco. The upper limit of 100 parts of moisture per 100 parts of tobacco is a practical preferred operating limit. The moistening operation can be carried out at ambient temperatures and also at elevated temperatures. It is usually preferred to maintain the tobacco below about 170 F. in order to avoid impairing flavor. In general, the moistening is carried out at ambient atmospheric temperatures such as 60 F. to F. The water can be added to the tobacco by any technique which results in a substantially uniform moistened mass, such as by spraying or soaking.
When the moisture content of the tobacco is within the desired range, the tobacco is then contacted with sufficient quantity of a volatile organic liquid for a time sufficient to accomplish thorough impregnation of the tobacco. The impregnation can be carried out at any suitable temperature but preferably is carried out at a temperature below about 170 F. in order to avoid impairing the flavor of the tobacco. It has been observed that the time needed to impregnate substantially uniformly the mass of tobacco is temperature dependent; also the time of impregnation is dependent upon the particle size of the tobacco. The larger the particle size the longer the time. The illustrative times for strips and shreds are: F., 0.5 to 1 hour; 100 F., 12-24 hours; 75 F., 40-100 hours.
A variety of organic liquids that can be evaporatively removed can be used for impregnation but preferably the or ganic liquid is one having a boiling point below that of water. lt is thought that in addition to helping to expand tobacco structure the inert organic liquid helps to set the cells in expanded condition. The organic liquidshould not be one which does combine irreversibly to a significant degree with the tobacco; in other words it must not alter the smoking qualities of the product to an undesirable extent, i.e., it should be chemically inert. Broadly the liquid falls into the classes of aliphatic hydrocarbons, aromatic hydrocarbons, alkanols, ketones, aliphatic esters, ethers, halogen substituted hydrocarbons and mixtures thereof. It is preferred to operate with the lower boiling members of these classes. lt is intended that lower boiling include those liquids having a boiling point below about 231 F. (1l0.7 C.) and preferably below about F. (68.5 C.).
Illustrative suitable inert organic liquids are: benzene and toluene; acetone, methyl ethyl ketone, methyl isopropyl ketone, diethyl ketone and diacetyl; methyl ethyl ether, diethyl ether, dipropyl ether, diisopropyl ether, methyl butyl ether, ethyl butyl ether, ethylene glycol dimethyl ether, and tetrahydrofuran; methanol, ethanol, propanol, isopropanol, sec-butyl alcohol, t-butyl alcohol, t-amyl alcohol, and allyl alcohol; butane, pentane, hexane, heptane, and the corresponding unsaturated hydrocarbons; and cyclobutane, cyclopentane, cyclohexane and cyclohexene.
The halogen substituted hydrocarbons may be aliphatic, cycloaliphatic or aromatic in nature. One or more halogen atoms may be present in each halohydrocarbon molecule. Two or more different halogens may be present in a single halohydrocarbon molecule. lllustrative halohydrocarbons are ethyl chloride, propyl chloride, isopropyl chloride, vinylidene chloride, n-butyl bromide, isobutyl chloride, sec-butyl chloride, t-butyl chloride, t-butyl bromide, methylene chloride, methylene bromide, chloroform, carbon tetrachloride, ethylene dichloride, ethylidene chloride,
acetylene dichloride, trichloroethylene and fluorobenzene.
Preferred classes of inert organic liquids are aliphatic hydrocarbons having 3 to 6 carbon atoms and the halogen substituted alkane hydrocarbons (halo-alkane) having l-2 carbon atoms and the halocycloalkanes having 3-4 carbon atoms. Those compounds generally known as Freon fluorocarbons are especially preferred. lllustrative of the preferred Freon liquids are trichloromonofluoromethane, dichlorodifluoromethane, monobromotrifluoromethane, monochlorodifluoromethane, dichlorotetrafluoroethane, tetrachlorodifluoroethane.
The amount of impregnating inert organic liquid is controlled for optimum results; broadly speaking it is between 15 parts of liquid per 100 parts of tobacco and about the maximum impregnation amount of liquid. The maximum impregnation amount is the maximum amount which can be taken up by the tobacco. In general the amount of impregnating liquid used is between about 25 parts and about 350 parts per 100 parts of tobacco. As with water there is a tendency to octafluorocyclobutane, vand trichlorotrifluoroethane,
impart mechanical difficulties in the handling of the tobacco impregnated with the higher amounts of liquid.
When operating with the preferred organic liquids it is preferred to use between about 40 and 250 parts per 100 parts of tobacco.
The temperature and pressure conditions under which the tobacco is contacted with the organic liquid are not critical, and generally speaking, ordinary room temperatures and pressures are entirely satisfactory. No special equipment is required for impregnating the tobacco with the inert organic liquid and impregnation can be carried out in any suitable type of tank, drum or other container. However, in the case of liquids having a low boiling point or high vapor pressure, the impregnation should be carried out at reduced temperatures or elevated pressures so that the liquid does not vaporize during the equilibration step.
After the tobacco has been thoroughly impregnated with the organic liquid the organic liquid is rapidly removed therefrom. This is accomplished by passing a hot gas through the impregnated tobacco to rapidly remove the organic liquid in a short period, such as on the order of a few seconds, as for example a period of less than about 4 seconds. in order to obtain the desired volume increase of tobacco and avoid impairing flavor quality, it is particularly advantageous to remove the organic impregnating liquid rapidly. Use of hot gas at a temperature of between 250 F. and 400 F. effectively removes the impregnating liquid very rapidly so as to cause expansion of the tobacco structure while avoiding shattering the tobacco into dust or fines. When processing cigarette cut filler, the expansion of the structure also causes delamination of laminated shreds which serves to increase the filling capacity and also improves the burning qualities of the filler. The organic liquid removal is preferably carried out at substantially atmospheric pressure but it can be carried out at super-atmospheric pressures when using very low boiling liquid. The gas is employed at a temperature at least about 200 F. higher than the boiling point of the organic liquid employed for impregnation. The temperature of the gas thus depends on the boiling point of the organic impregnating liquid. It is preferred to avoid use of gas temperatures higher than about 400 F. so as to avoid flavor impairment of the tobacco composition. The gas is preferably maintained at a temperature below about 350 F. The hot gas is preferably a mixture of vaporized organic liquid and steam, but other hot gases such as, for example, air, nitrogen, carbon dioxide, gaseous organic liquid or mixtures thereof or any other gas which is inert with respect to the tobacco and the volatile organic impregnating liquid can be advantageously employed.
After evaporative removal of the organic impregnating liquid from the tobacco the organic liquid can be recovered, condensed and recycled for further use. The expanded tobacco is then reordered to the water content desired for the particular end use. By reordering it is meant that the moisture content ofthe expanded tobacco is adjusted to a desired value such as, for example, 12-13% for cut filler for cigarette makmg.
The process of the invention is further described with reference to the drawing, the single figure of which illustrates in block diagrammatic form an embodiment of the process of the invention.
Tobacco moistener l is a unit adapted for adding water from line 2 to cured tobacco feed from line 3. Moistener 1 may add the water by means of spraying, or passage through a pool of water with provisions made for draining off excess water and for a period of time during which the water diffuses throughout the mass of tobacco. ln order to maintain the water soluble components in the tobacco, any water which is drained from the moist tobacco is recycled by way of line 2, thus preventing net extraction of soluble material from the tobacco. In some instances the tobacco may already have a moisture content equal to the desired water content of the moist tobacco. In this case moistener 1 would be bypassed (by way ofline 3A The moist tobacco is passed by way of conveyor line 4 to impregnator 6 which can, for example, be a closed cylinder provided with a screw for moving the moist tobacco therethrough. Here the moist tobacco is impregnated with organic liquid from line 7. The organic liquid can be added in much the same manner as is the water in moistener 1. Also, any drained liquid from impregnator 6 is recycled (via line 7A) to line 7 in order to reduce losses of liquid soluble components from the tobacco. lmpregnator 6 is adapted to operate at moderately elevated temperatures such as F usually at autogenous pressure. lmposed pressures can be used to help maintain the organic liquid in the liquid state and to increase the impregnation rate. lllustratively, 700 pounds of cut filler tobacco, pounds of water and 1200 pounds of Freon 11 can be introduced into impregnator 6 with the tobacco remaining in the impregnator for approximately 30 minutes.
The moist, impregnated tobacco is then passed by way of line 8 to line 9 for introduction into tobacco expander 13. A gaseous mixture such as Freon and steam is passed from gas heater 11 by way of line 9 into expander 13 where the hot gas and the moist impregnated tobacco are thoroughly intermingled. A sufficient flow of gas is used to effect evaporative removal of the impregnated liquid from the tobacco at a rapid rate. Fan 12 is employed for flowing the hot gas through expander 13. lllustratively, when expanding 700 pounds of moist, impregnated tobacco per hour a gaseous mixture of 280,000 pounds of Freon 11 and 38,700 pounds of steam per hour are introduced into expander 13 at a temperature of about 340 F. and a linear velocity of approximately 27 feet per second. With an expander unit of 84 feet in height, the moist impregnated tobacco is contacted with the hot gas for approximately 3.1 seconds.
In expander unit 13 the tobacco is expanded (increased in filling capacity) with the hot gas carrying the expanded tobacco into separator 14. Separator 14 can be any conventional form of separator such as a cyclone type. The expanded tobacco product is withdrawn from separator 14 by way of line 16 and passed, if desired, for processing economy, into a residual liquid removal operation in unit 17. Conveniently the expanded tobacco is contacted with steam introduced through line 18 in an amount sufficient to vaporize all of the residual organic liquid. The condensed steam from residual removal operation 17 is passed by way of line 19 to a recovery operation for recovery of the organic liquid content.
Normally, the organic liquid-free tobacco from residual liquid removal operation 17 is reordered to a water content suitable for storage or immediate use. If reordering is desired, the liquid-free tobacco is passed to reordering operation 21 where it is brought to the desired moisture content by drying or moistening operations well known to the tobacco industry. The reordered expanded tobacco composition (product) is then passed to storage for subsequent use through line 22.
The heating gas and organic liquid vapor and water vapor removed from the moist impregnated tobacco are recycled from separator 14 via line 28 to gas heater 11, thence to expander 13 via line 9. Excess gases from the recycle circuit are bled by way of line 23 into liquid recovery operation 24. Here the water and liquid are condensed. Water is removed by way of line 26 and organic liquid is recycled to impregnator 6 by way of line 27. Where organic liquid immiscible with water is employed, simple decantation is used for separation. Distillation is used for recovery of organic liquids which are miscible with water.
The significant increase in the filling capacity of tobacco achieved in accordance with this invention is readily apparent from the data of the following examples. In order to measure the filling capacity of a cut filler tobacco product as described in the following examples, a compressometer is used which is essentially composed of a cylinder 9.5 centimeters in diameter with a graduated scale on the side. A piston 9.4 centimeters in diameter slides in the cylinder. Pressure is applied to the piston and volume in milliliters of a given weight of tobacco, 100 grams, is determined. Experiments have shown that this EXAMPLE 1 Regular blended cigarette cut filler, 4500 grams containing 12.7% moisture (14.5 parts of water per 100 parts of tobacco), was sprayed with 1125 milliliters of water and bulked one hour. The moist tobacco was dipped in F reon-MF liquid utilizing a total of 8 liters of the liquid (300 parts of Freon-MF per 100 parts of tobacco). The tobacco was sealed in a pressure vessel, which was then heated 75 minutes by water at 133 F internal pressure was 30 pounds per square inch, gauge, at the end of the heating period. The vessel was then cooled by water at 50 F. for minutes, and 2650 milliliters of excess liquid Freon-MF was drained from the vessel affording a net impregnation of 201 parts of F reon-MF per 100 parts of tobacco. The tobacco was then intimately contacted in a vertical column with a hot gas mixture, comprising air, water vapor, and gaseous Freon-MF, at a gas inlet temperature of 330 F. for a contact time of about 2 seconds. Tobacco from the hot gas contacting was reordered with a water spray and bulked overnight (allowed to stand in a closed vessel overnight to equilibrate the moisture).
Percent Filling Increased Percent Capacity, Filling Moisture m1./100 g. Capacity Control- 12. 7 422 Treated product 12. 4 596 41 EXA M PLE 2 Regular blended cigarette cut filler, 4500 grams containing 12.7% moisture, was sprayed with 450 milliliters of water and bulked overnight (26 parts of water per 100 parts of tobacco). The moist tobacco was dipped in Freon-MF liquid comprising that drained from a previous run, utilizing a total of 8 liters of the liquid (300 parts of Freon-MF per 100 parts of tobacco). The tobacco was sealed in a pressure vessel, which was then heated for 90 minutes by water at 133 F.; internal pressure was 31 pounds per square inch, gauge, at the end of the heating period. The vessel was then cooled by water at 50 F. for minutes, and 3150 milliliters of excess liquid Freon-MF was drained from the vessel providing a net impregnation of 182 parts of Freon-MF per 100 parts of tobacco. The tobacco was then intimately contacted in a vertical column with a hot gas mixture, comprising air, water vapor, and Freon-MF gas, at a gas inlet temperature of 330 F. for a contact time of about 1 second. Tobacco feed rate was uniform over a period of 20 minutes. Tobacco from the hot gas contacting was reordered with'a water spray and bulked overnight.
Regular blended cigarette cut filler, 4500 grams containing 12.1% moisture, was sprayed with 225 milliliters of water and bulked overnight (19.3 parts of water per 100 parts of tobac co). The moist tobacco was dipped in Freon-MF liquid com- 75 Treated product prising that drained from a previous run, using a total of 8 liters of the liquid (298 parts of Freon-MF per 100 parts of tobacco). The tobacco was sealed in a pressure vessel, which was then heated for 90 minutes by water at 133 F. The vessel was then cooled by water at 50 F. for 40 minutes, and 4200 milliliters of excess liquid Freon-MF was drained from the vessel providing a net impregnation of 142 parts of Freon-MF per 100 parts of tobacco. The tobacco was then intimately contactcd by passing it through a vertical column with a hot gas mixture, comprising air, water vapor, and Freon-MFgas, at a gas inlet temperature of 341 F. for a contact time of about 0.75 seconds. Tobacco from the hot gas contacting was reordered with a water spray and bulked overnight.
Flue-cured cut filler, 5700 grams containing 11.3% moisture, was sprayed with 570 milliliters of water and bulked 25 one hour (24 parts water per 100 parts of tobacco). The moist tobacco was dipped in Freon-MF liquid comprising that drained from a previous run, using a total of 12 liters of the liquid (350 parts Freon-MF per 100 parts of tobacco). The tobacco was sealed ina pressure vessel, which was then heated for 90 minutes by water at 134 F.; internal pressure was 37 pounds per square inch, gauge, at the end of the heating period. The vessel was then cooled by water at F. for 12 minutes and 3100 milliliters of excess liquid Freon-MF was 35 drained from the vessel giving a net impregnation of 259 parts of Freon-MF per 100 parts of tobacco. The tobacco was then intimately contacted by passing it through a vertical column with a hot gas mixture comprising air, water vapor, and F reon- MF gas, at a gas inlet temperature of 343 F. for a contact time M 0 of about 0.7 seconds. Tobacco feed rate was uniform over a period-of 17 minutes. Tobacco from the hot gas contacting was reordered with a water spray and bulked overnight.
Treated product 5 0 EXAMPLE 5 Burley cut filler, 3920 grams containing 11.6% moisture, was sprayed with 392 milliliters of water and bulked overnight (24.4 parts of water per 100 parts of tobacco). The moist tobacco was dipped in Freon-MF liquid comprising that drained from a previous run, using a total of 7 liters of the I liquid. The tobacco was sealed in a pressure vessel, which was then heated for 90 minutes by water at 127 F internal pressure was 26 pounds per square inch, gauge, at the end of the heating period. The vessel was then cooled by water at 50 F.
for 20 minutes, and 2700 milliliters of excess liquid Freon-MF was drained from the vessel. The tobacco was then intimately contacted by passing it through a vertical column with a hot gas mixture, comprising air, water vapor, and F reon-MF gas,
at a gas inlet temperature of 335 F. for a contact time of about 0.7 seconds. Tobacco feed rate was uniform over a period of 7 minutes. Tobacco from the hot gas contacting was reordered with a water spray and bulked overnight.
Percent Filling Increased Percent Capacity, Filling Moisture mL/IOO g. Capacity Control 11.6 427 ..L
Turkish cut filler, 5700 grams containing 11.6% moisture was sprayed with 570 milliliters of water and bulked one hour (24.4 parts water per 100 parts of tobacco). The moist tobacco was dipped in Freon-MF liquid comprising that drained from a previous run, using a total of 11 liters of the liquid (322 parts Freon-MF per 100 parts of tobacco). The tobacco was sealed in a pressure vessel, which was then heated for 90 minutes by water at 127 F.; internal pressure was 27 pounds per square inch, gauge, at the end of the heating period. The vessel was then cooled by water at 50 F. for 12 minutes, and 4500 milliliters of excess liquid Freon-MF was drained from the vessel giving a net impregnation of 190 parts of Freon-M F per 100 parts of tobacco. The tobacco was then intimately contacted by passing it through a vertical column with a hot gas mixture, comprising air, water vapor, and Freon-MF gas, at a gas inlet temperature of 339 F. for a contact time of about 0.7 seconds. Tobacco feed rate was uniform over a period of 13 minutes. Tobacco from the hot gas contacting was reordered with a water spray and bulked overnight.
Regular blended cigarette cut filler, 5700 grams containing 18.75% moisture, was dipped in Freon-MF liquid comprising that drained from a previous run, using a total of liters of the liquid (318 parts Freon-MF per 100 parts of tobacco). The tobacco was sealed in a pressure vessel, which was then heated for 45 minutes by water at 149 F.; internal pressure was 40 pounds per square inch, gauge, at the end of the heating period. The vessel was then cooled by water at 50 F. for minutes, and 4950 milliliters of excess liquid Freon-MF was drained from the vessel giving a net impregnation of 161 parts of Freon-MF per 100 parts of tobacco. The tobacco was then intimately contacted by passing it through a vertical column with a hot gas mixture, comprising air, water vapor, and Freon-MF gas, at a gas inlet temperature of 347 F. for a contact time of about 0.7 seconds. The tobacco feed rate was uniform over a period of 16 minutes. Tobacco from the hot gas contacting was reordered with a water spray and bulked overnight.
Regular blended cigarette cut filler, 5700 grams containing 18.85% moisture, was placed in a pressure vessel, and 8 liters of Freon-MF liquid, comprising that drained from a previous run, was introduced into the vessel (225 parts Freon-MF per 100 parts of tobacco). The vessel was sealed and heated for one hour by water at 149 F.; internal pressure was 39 pounds per square inch, gauge, at the end of the heating period. The vessel was then cooled by water at 50 F. for 8 minutes, and 4300 milliliters of excess liquid Freon-MF was drained from the vessel giving a net impregnation of 118 parts of Freon-MF per 100 parts of tobacco. The impregnated tobacco was then intimately contacted by passing it through a vertical column with a hot gas mixture, comprising air, water vapor, and Freon-MF gas, at a gas inlet temperature of 347 F. for a contact time of about 0.7 seconds. The tobacco feed rate was uniform over a period of 13 minutes. Tobacco from the hot gas contacting was reordered with a water spray and bulked overnight.
Regular blended cigarette cut filler, 5700 grams containing 18.1% moisture, was placed in a pressure vessel and 8 liters of Freon-MF liquid, comprising that drained from a previous run, was poured over the tobacco, and 2700 milliliters of excess liquid Freon-MF was drained from the vessel. The vessel was then sealed and heated for one hour by water at 151 F.; internal pressure was 39 pounds per square inch, gauge, at the end ofthe heating period. The vessel was then cooled by water at 50 F. for 11 minutes, and 2400 milliliters more excess liquid Freon-MF was drained from the vessel. The impregnated tobacco was then intimately contacted by passing it through a vertical column with a hot gas mixture, comprising air, water vapor, and Freon-MF gas, at a gas inlet temperature of 347 F. for a contact time of the tobacco with the hot gases ofabout 0.7 seconds. The tobacco feed rate was uniform over a period of 12 l/4 minutes. Tobacco from the hot gas contacting was cooled and reordered with a water spray, and bulked overnight.
Flue-cured cut filler, 5700 grams containing 17.3% moisture, was placed in a pressure vessel, and 10 liters of Freon-MF liquid, comprising that drained from a previous run, was poured over the tobacco (313 parts Freon-MF per parts of tobacco). The vessel was sealed and heated for one hour by water at 147 F.; internal pressure was 40 pounds per square inch, gauge, at the end of the heating period. The vessel was then cooled by water at 50 F. for 16 minutes, and 4000 milliliters of excess liquid Freon-MF was drained from the vessel giving a net impregnation of 188 parts of Freon-MF per 100 parts of tobacco. The liquid-impregnated tobacco was then intimately contacted by passing it through a vertical column with a hot gas mixture, comprising air, water vapor, and Freon-MF gas, at a gas inlet temperature of 343 F. for a contact time of about 0.65 seconds. The tobacco feed rate was uniform over a period of 12 3/4 minutes. Tobacco from the hot gas contacting was cooled, and reordered with a water spray, and bulked overnight.
Flue-cured cut filler, 5700 grams containing 17.6% moisture, was placed in a pressure vessel and 8 liters of Freon- MF liquid, comprising that drained from a previous run, was poured over the tobacco, and 2000 milliliters of excess liquid Freon-MF was drained from the vessel. The vessel was then sealed and heated for one hour by water at 151 F.; internal Control 11. 3 463 pressure was 31 pounds per square inch, gauge, at the end of the heating period. The vessel was then cooled by water at 50 F. for 6 minutes, and 1500 milliliters more excess liquid Freon-MF was drained from the vessel. The tobacco was then intimately contacted by passing it through a vertical column with a flowing hot gas mixture, comprising air, water vapor, and Freon-MF gas, at a gas inlet temperature of 339 F. for a contact time of tobacco with hot gas of about 0.65 seconds. The tobacco feed rate was uniform over a period of 10 minutes. Tobacco from the hot gas contacting was reordered with a water spray and bulked overnight.
Percent Increased Capacity, Filling Moisture ml./100 g. Capacity Control 11. 3 463 Treated product 12. 3 704 52 Filling Percent EXAMPLE l2 Flue-cured cut filler, 5700 grams containing 17.4% moisture, was placed in a pressure vessel, and 6 liters of Freon-MF liquid, comprising that drained from a previous run, was poured over the tobacco. The vessel was sealed and heated for one hour by water at 145 F.; internal pressure was 33 pounds per square inch, gauge, at the end of the heating period. The vessel was then cooled by water at 50 F. for 10 minutes, and 2000 milliliters of excess liquid Freon-MF was Percent Increased Filling Capacity Filling Capacity, mL/IOO g.
Percent Moisture Treated product 12. 0 720 56 EXAMPLE l3 Flue-cured cut filler, 5700 grams, was placed in a pressure vessel and 28 liters of a mixture consisting of three parts Freon-MF and one part isopropanol, by volume, was poured over the tobacco. The vessel was then sealed and heated for one hour by hot water (140 F.); internal pressure was 60 pounds per square inch, gauge, at the end of the heating period. Pressure was relieved by draining off the excess liquid with consequent flashing off of vapors; 13.2 liters of the liquid was collected. The vessel was further cooled by tap water and an additional 2.3 liters of excess liquid drained from the vessel. The treated tobacco was then intimately contacted with a flowing hot gas mixture, comprising air, water vapor, isopropanol vapor, and Freon-MF gas. Tobacco from the hot gas contacting was reordered with a water spray and bulked overnight.
Percent Increased Filling Capacity Filling Percent Capacity, Moisture mL/lOO g.
Control 387 Treated product 1 Including alcohol.
The process of the present invention can be applied to cured tobacco in the form of leaf (including veins and stems), strips (leaf with stems removed) or cut filler (strips shredded for cigarette making). By using leaf or strips, the types or grades of tobacco can be selected for which the process is most effective, thereby achieving results near the maximum while holding processing costs to a minimum. Where treatment of stems is not necessary, strips are preferred rather than leaf, and in any event stems can be processed separately. If the entire blend is to be treated, then cut filler is preferably utilized.
The advantages of the invention are readily apparent from the foregoing. By the process of the invention, the filling capacity of tobacco can be significantly increased with the attending economic advantages. Vaporization and removal of the organic liquid from the impregnated tobacco at high temperatures and short contact times permits the advantages of the invention to be realized with the use of minimum size equipment and with high production rates.
Those modifications and equivalents which fall within the spirit of the invention and the scope of the appended claims are to be considered part of the invention.
We claim:
1. A process of increasing the filling capacity of tobacco which comprises providing a stream of tobacco moistened with a volatile organic liquid, flowing said moistened tobacco stream into a rapidly moving stream of a gas heated to a temperature substantially above the boiling point of the organic liquid at the prevailing pressure whereby the liquid is rapidly volatilized and the tobacco is expanded in a period of less than about 4 seconds, and separating the expanded tobacco from the hot gas and volatized liquid stream.
2. The process of Claim 1 in which the organic liquid is a halogenated hydrocarbon.
3. The process of Claim 1 in which the organic liquid is trichloromonofluoromethane. I
4. The process of Claim 1 in which the amount of organic liquid in the moistened tobacco flowed to the gas stream is at least 15 parts by weight of liquid per parts by weight of tobacco (dry basis).
5. The process of Claim 1 wherein at least a portion of the volatized liquid separated from the expanded tobacco is heated and recycled as the gas stream into which said moistened tobacco is flowed.
6. A process of increasing the filling capacity of tobacco which comprises contacting tobacco having a moisture content of between 10 and 100 parts of water per 100 parts of tobacco (dry basis) with a volatile organic liquid in an amount to impregnate the moist tobacco with said liquid, suspending the moist tobacco impregnated with said organic liquid in a stream of rapidly moving gas heated to a temperature substantially above the boiling point of the organic liquid at the prevailing pressure whereby the organic liquid is rapidly vaporized within the tobacco and the tobacco is expanded in a period of less than about 4 seconds, and then separating the tobacco from the gas stream containing vapors of said organic liquid.
7. The process recited in Claim 6 wherein the last mentioned gas stream including said vapors is at least in part heated and recycled to form at least a part of the first mentioned stream in which the tobacco is suspended.
8. The process of Claim 6 in which the tobacco has an initial moisture content of between 13 and 50 parts of water per 100 parts of tobacco (dry basis) and the organic liquid content of the impregnated tobacco when initially contacted with the hot suspending gas is in excess of about 15 parts per 100 parts of tobacco (dry basis).
9. The process of Claim 6 in which the tobacco is shredded tobacco.
10. The process of Claim 6 in which the tobacco is shredded tobacco and the amount of organic liquid in the moistened tobacco when initially suspended in the hot gas is between about 25 and 350 parts of liquid per 100 parts of tobacco (dry basis).
Priority Applications (15)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US720068A US3524452A (en) | 1968-04-10 | 1968-04-10 | Process for increasing the filling capacity of tobacco |
| IE358/69A IE32990B1 (en) | 1968-04-10 | 1969-03-19 | Process for preparing tobacco |
| GB05117/69A GB1222308A (en) | 1968-04-10 | 1969-03-21 | Process for preparing tobacco |
| IL31884A IL31884A (en) | 1968-04-10 | 1969-03-24 | Process for increasing filling capacity of tobacco |
| NO1375/69A NO122519B (en) | 1968-04-10 | 1969-04-01 | |
| DE19691917552 DE1917552C3 (en) | 1968-04-10 | 1969-04-01 | Process for increasing the filling capacity of tobacco |
| SE04711/69A SE348358B (en) | 1968-04-10 | 1969-04-02 | |
| DK186969AA DK123803B (en) | 1968-04-10 | 1969-04-02 | Method for increasing the fullness of tobacco. |
| FI690988A FI49105C (en) | 1968-04-10 | 1969-04-03 | Procedure for increasing the filling capacity of tobacco. |
| CH517369A CH509047A (en) | 1968-04-10 | 1969-04-03 | Process for increasing the filling capacity of tobacco |
| NL6905416A NL137540C (en) | 1968-04-10 | 1969-04-08 | |
| FR6911125A FR2006020A1 (en) | 1968-04-10 | 1969-04-10 | |
| CH379170A CH536606A (en) | 1968-04-10 | 1970-03-13 | Increasing the packing bulk of tobacco |
| FR7147735A FR2119789A6 (en) | 1968-04-10 | 1971-12-31 | Tobacco treatment process |
| MY197262A MY7200062A (en) | 1968-04-10 | 1972-12-31 | Process for preparing tobacco |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US720068A US3524452A (en) | 1968-04-10 | 1968-04-10 | Process for increasing the filling capacity of tobacco |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3524452A true US3524452A (en) | 1970-08-18 |
Family
ID=24892505
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US720068A Expired - Lifetime US3524452A (en) | 1968-04-10 | 1968-04-10 | Process for increasing the filling capacity of tobacco |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US3524452A (en) |
Cited By (37)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3612066A (en) * | 1970-02-05 | 1971-10-12 | Reynolds Tobacco Co R | Denicotinizing process |
| US3710803A (en) * | 1969-10-15 | 1973-01-16 | Research Corp | Method for turgor conditioning tobacco |
| US3765425A (en) * | 1971-09-02 | 1973-10-16 | Brown & Williamson Tobacco Corp | Puffing of tobacco |
| US3881498A (en) * | 1971-01-27 | 1975-05-06 | Hauni Werke Koerber & Co Kg | Apparatus for increasing the volume of moist tobacco |
| US3882874A (en) * | 1969-09-22 | 1975-05-13 | Reynolds Tobacco Co R | Tobacco expansion process |
| US3957063A (en) * | 1971-01-27 | 1976-05-18 | Hauni-Werke Korber & Co., Kg | Method and apparatus for increasing the volume of moist tobacco |
| US3978867A (en) * | 1971-01-27 | 1976-09-07 | Hauni-Werke Korber & Co., Kg | Apparatus for increasing the volume of moist tobacco |
| US4076030A (en) * | 1975-12-22 | 1978-02-28 | R. J. Reynolds Tobacco Company | Method for utilizing tobacco stems in smoking products |
| US4095605A (en) * | 1976-09-02 | 1978-06-20 | Reynolds Leasing Corporation | Recovery system for use with a batch process for increasing the filling capacity of tobacco |
| US4148325A (en) * | 1975-08-18 | 1979-04-10 | British-American Tobacco Company Limited | Treatment of tobacco |
| US4167191A (en) * | 1977-09-27 | 1979-09-11 | Brown & Williamson Tobacco Corporation | Tobacco drying process |
| US4195647A (en) * | 1977-09-03 | 1980-04-01 | Hauni-Werke Korber & Co. Kg. | Method and apparatus for increasing the volume of tobacco or the like |
| US4202357A (en) * | 1978-10-27 | 1980-05-13 | Philip Morris Incorporated | Reordering expanded tobacco by water mist |
| US4211243A (en) * | 1977-02-22 | 1980-07-08 | Kikkoman Shoyu Co., Ltd. | Process for producing expanded tobacco stems |
| US4336814A (en) * | 1977-08-08 | 1982-06-29 | Philip Morris Incorporated | Process for expanding tobacco |
| US4388932A (en) * | 1980-12-31 | 1983-06-21 | Philip Morris, Incorporated | Process for improving filling power of expanded tobacco |
| US4532945A (en) * | 1982-09-21 | 1985-08-06 | Philip Morris Incorporated | Process for increasing and maintaining the filling power of tobacco |
| USRE32014E (en) * | 1977-08-08 | 1985-10-29 | Philip Morris, Inc. | Process for expanding tobacco |
| US4821747A (en) * | 1986-04-23 | 1989-04-18 | R. J. Reynolds Tobacco Company | Process for treating tobacco and similar organic materials |
| US5031644A (en) * | 1989-12-29 | 1991-07-16 | R. J. Reynolds Tobacco Company | Tobacco expansion process and product |
| US5056537A (en) * | 1989-09-29 | 1991-10-15 | R. J. Reynolds Tobacco Company | Cigarette |
| US5065774A (en) * | 1989-08-18 | 1991-11-19 | R. J. Reynolds Tobacco Company | Process for expanding tobacco under moderate conditions |
| US5076293A (en) * | 1989-06-19 | 1991-12-31 | R. J. Reynolds Tobacco Company | Process and apparatus for the treatment of tobacco material |
| US5095922A (en) * | 1990-04-05 | 1992-03-17 | R. J. Reynolds Tobacco Company | Process for increasing the filling power of tobacco material |
| US5095923A (en) * | 1991-04-11 | 1992-03-17 | R. J. Reynolds Tobacco Company | Tobacco expansion process using 1,1,1,2-tetrafluoroethane |
| US5259403A (en) * | 1992-03-18 | 1993-11-09 | R. J. Reynolds Tobacco Company | Process and apparatus for expanding tobacco cut filler |
| EP0629353A3 (en) * | 1993-06-14 | 1995-05-31 | Reynolds Tobacco Co R | Tobacco expansion method and apparatus. |
| US5497794A (en) * | 1993-03-29 | 1996-03-12 | Japan Tobacco Inc. | Cigarette |
| US5590667A (en) * | 1995-07-28 | 1997-01-07 | Scw, Inc. | Tobacco expansion method |
| US5819754A (en) * | 1995-12-29 | 1998-10-13 | R. J. Reynolds Tobacco Company | Tobacco expansion processes and apparatus |
| US6067994A (en) * | 1997-10-07 | 2000-05-30 | R.J. Reynolds Tobacco Company | Tobacco expansion batch forming, unloading and expansion agent purging process and apparatus |
| DE3725309C2 (en) * | 1986-08-01 | 2002-10-02 | American Tobacco Co | Method and device for expanding tobacco |
| US20040182404A1 (en) * | 2003-03-20 | 2004-09-23 | Poindexter Dale Bowman | Method of expanding tobacco using steam |
| RU2306093C1 (en) * | 2006-03-21 | 2007-09-20 | Олег Иванович Квасенков | Method for producing of exploded tobacco |
| EP2692247A4 (en) * | 2011-03-31 | 2014-11-12 | Japan Tobacco Inc | DEVICE AND METHOD FOR EXPANSION OF TOBACCO |
| US9986753B2 (en) | 2016-10-06 | 2018-06-05 | Alfonso Campalans | Quad apparatus, method and system |
| WO2024143892A1 (en) | 2022-12-27 | 2024-07-04 | 주식회사 케이티앤지 | Smoking material including expanded shred tobacco, method for preparing same, and smoking article comprising same |
-
1968
- 1968-04-10 US US720068A patent/US3524452A/en not_active Expired - Lifetime
Cited By (39)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3882874A (en) * | 1969-09-22 | 1975-05-13 | Reynolds Tobacco Co R | Tobacco expansion process |
| US3710803A (en) * | 1969-10-15 | 1973-01-16 | Research Corp | Method for turgor conditioning tobacco |
| US3612066A (en) * | 1970-02-05 | 1971-10-12 | Reynolds Tobacco Co R | Denicotinizing process |
| US3881498A (en) * | 1971-01-27 | 1975-05-06 | Hauni Werke Koerber & Co Kg | Apparatus for increasing the volume of moist tobacco |
| US3957063A (en) * | 1971-01-27 | 1976-05-18 | Hauni-Werke Korber & Co., Kg | Method and apparatus for increasing the volume of moist tobacco |
| US3978867A (en) * | 1971-01-27 | 1976-09-07 | Hauni-Werke Korber & Co., Kg | Apparatus for increasing the volume of moist tobacco |
| US3765425A (en) * | 1971-09-02 | 1973-10-16 | Brown & Williamson Tobacco Corp | Puffing of tobacco |
| US4148325A (en) * | 1975-08-18 | 1979-04-10 | British-American Tobacco Company Limited | Treatment of tobacco |
| US4076030A (en) * | 1975-12-22 | 1978-02-28 | R. J. Reynolds Tobacco Company | Method for utilizing tobacco stems in smoking products |
| US4095605A (en) * | 1976-09-02 | 1978-06-20 | Reynolds Leasing Corporation | Recovery system for use with a batch process for increasing the filling capacity of tobacco |
| US4211243A (en) * | 1977-02-22 | 1980-07-08 | Kikkoman Shoyu Co., Ltd. | Process for producing expanded tobacco stems |
| US4336814A (en) * | 1977-08-08 | 1982-06-29 | Philip Morris Incorporated | Process for expanding tobacco |
| USRE32014E (en) * | 1977-08-08 | 1985-10-29 | Philip Morris, Inc. | Process for expanding tobacco |
| US4195647A (en) * | 1977-09-03 | 1980-04-01 | Hauni-Werke Korber & Co. Kg. | Method and apparatus for increasing the volume of tobacco or the like |
| US4167191A (en) * | 1977-09-27 | 1979-09-11 | Brown & Williamson Tobacco Corporation | Tobacco drying process |
| US4202357A (en) * | 1978-10-27 | 1980-05-13 | Philip Morris Incorporated | Reordering expanded tobacco by water mist |
| US4388932A (en) * | 1980-12-31 | 1983-06-21 | Philip Morris, Incorporated | Process for improving filling power of expanded tobacco |
| US4532945A (en) * | 1982-09-21 | 1985-08-06 | Philip Morris Incorporated | Process for increasing and maintaining the filling power of tobacco |
| US4821747A (en) * | 1986-04-23 | 1989-04-18 | R. J. Reynolds Tobacco Company | Process for treating tobacco and similar organic materials |
| US4944316A (en) * | 1986-04-23 | 1990-07-31 | Oskar Stuhl | Process for treating tobacco and similar organic materials |
| DE3725309C2 (en) * | 1986-08-01 | 2002-10-02 | American Tobacco Co | Method and device for expanding tobacco |
| US5076293A (en) * | 1989-06-19 | 1991-12-31 | R. J. Reynolds Tobacco Company | Process and apparatus for the treatment of tobacco material |
| US5065774A (en) * | 1989-08-18 | 1991-11-19 | R. J. Reynolds Tobacco Company | Process for expanding tobacco under moderate conditions |
| US5056537A (en) * | 1989-09-29 | 1991-10-15 | R. J. Reynolds Tobacco Company | Cigarette |
| US5031644A (en) * | 1989-12-29 | 1991-07-16 | R. J. Reynolds Tobacco Company | Tobacco expansion process and product |
| US5095922A (en) * | 1990-04-05 | 1992-03-17 | R. J. Reynolds Tobacco Company | Process for increasing the filling power of tobacco material |
| US5095923A (en) * | 1991-04-11 | 1992-03-17 | R. J. Reynolds Tobacco Company | Tobacco expansion process using 1,1,1,2-tetrafluoroethane |
| US5259403A (en) * | 1992-03-18 | 1993-11-09 | R. J. Reynolds Tobacco Company | Process and apparatus for expanding tobacco cut filler |
| US5497794A (en) * | 1993-03-29 | 1996-03-12 | Japan Tobacco Inc. | Cigarette |
| EP0629353A3 (en) * | 1993-06-14 | 1995-05-31 | Reynolds Tobacco Co R | Tobacco expansion method and apparatus. |
| US5590667A (en) * | 1995-07-28 | 1997-01-07 | Scw, Inc. | Tobacco expansion method |
| US5819754A (en) * | 1995-12-29 | 1998-10-13 | R. J. Reynolds Tobacco Company | Tobacco expansion processes and apparatus |
| US6067994A (en) * | 1997-10-07 | 2000-05-30 | R.J. Reynolds Tobacco Company | Tobacco expansion batch forming, unloading and expansion agent purging process and apparatus |
| US20040182404A1 (en) * | 2003-03-20 | 2004-09-23 | Poindexter Dale Bowman | Method of expanding tobacco using steam |
| US7556047B2 (en) | 2003-03-20 | 2009-07-07 | R.J. Reynolds Tobacco Company | Method of expanding tobacco using steam |
| RU2306093C1 (en) * | 2006-03-21 | 2007-09-20 | Олег Иванович Квасенков | Method for producing of exploded tobacco |
| EP2692247A4 (en) * | 2011-03-31 | 2014-11-12 | Japan Tobacco Inc | DEVICE AND METHOD FOR EXPANSION OF TOBACCO |
| US9986753B2 (en) | 2016-10-06 | 2018-06-05 | Alfonso Campalans | Quad apparatus, method and system |
| WO2024143892A1 (en) | 2022-12-27 | 2024-07-04 | 주식회사 케이티앤지 | Smoking material including expanded shred tobacco, method for preparing same, and smoking article comprising same |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| AS | Assignment |
Owner name: ARJAY HOLDINGS, INC., 1036 ELKTON ROAD, NEWARK, DE Free format text: ASSIGNMENT OF ASSIGNORS INTEREST.;ASSIGNOR:REYNOLDS LEASING CORPORATION;REEL/FRAME:004273/0242 Effective date: 19840507 |