US3524451A - Process for increasing the filling capacity of tobacco - Google Patents
Process for increasing the filling capacity of tobacco Download PDFInfo
- Publication number
- US3524451A US3524451A US720406A US72040668A US3524451A US 3524451 A US3524451 A US 3524451A US 720406 A US720406 A US 720406A US 72040668 A US72040668 A US 72040668A US 3524451 A US3524451 A US 3524451A
- Authority
- US
- United States
- Prior art keywords
- tobacco
- liquid
- filling capacity
- percent
- milliliters
- 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 102
- 235000002637 Nicotiana tabacum Nutrition 0.000 title description 102
- 238000000034 method Methods 0.000 title description 39
- 239000007788 liquid Substances 0.000 description 68
- 239000007789 gas Substances 0.000 description 23
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 17
- 238000009835 boiling Methods 0.000 description 12
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 9
- 235000019504 cigarettes Nutrition 0.000 description 9
- 239000002245 particle Substances 0.000 description 7
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- 239000000945 filler Substances 0.000 description 6
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
- 238000010025 steaming Methods 0.000 description 6
- 230000008016 vaporization Effects 0.000 description 6
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 5
- 238000005470 impregnation Methods 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 235000019505 tobacco product Nutrition 0.000 description 5
- 238000009834 vaporization Methods 0.000 description 5
- 239000012467 final product Substances 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-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 aliphatic alcohols Chemical class 0.000 description 3
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 235000019506 cigar Nutrition 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000011067 equilibration Methods 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 210000003462 vein Anatomy 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
- XXROGKLTLUQVRX-UHFFFAOYSA-N allyl alcohol Chemical compound OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- BTANRVKWQNVYAZ-UHFFFAOYSA-N butan-2-ol Chemical compound CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 description 2
- HGCIXCUEYOPUTN-UHFFFAOYSA-N cyclohexene Chemical compound C1CCC=CC1 HGCIXCUEYOPUTN-UHFFFAOYSA-N 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- FDPIMTJIUBPUKL-UHFFFAOYSA-N pentan-3-one Chemical compound CCC(=O)CC FDPIMTJIUBPUKL-UHFFFAOYSA-N 0.000 description 2
- 230000000391 smoking effect Effects 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 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
- HFGHRUCCKVYFKL-UHFFFAOYSA-N 4-ethoxy-2-piperazin-1-yl-7-pyridin-4-yl-5h-pyrimido[5,4-b]indole Chemical compound C1=C2NC=3C(OCC)=NC(N4CCNCC4)=NC=3C2=CC=C1C1=CC=NC=C1 HFGHRUCCKVYFKL-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 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
- 241000220010 Rhode Species 0.000 description 1
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical group ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 238000007605 air drying Methods 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 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
- 230000000052 comparative effect Effects 0.000 description 1
- 239000013068 control sample Substances 0.000 description 1
- 150000004292 cyclic ethers Chemical class 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
- 229960003750 ethyl chloride Drugs 0.000 description 1
- 239000000796 flavoring agent Substances 0.000 description 1
- 235000019634 flavors Nutrition 0.000 description 1
- 238000013467 fragmentation Methods 0.000 description 1
- 238000006062 fragmentation reaction Methods 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- DMEGYFMYUHOHGS-UHFFFAOYSA-N heptamethylene Natural products C1CCCCCC1 DMEGYFMYUHOHGS-UHFFFAOYSA-N 0.000 description 1
- 150000002430 hydrocarbons Chemical class 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 class 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- VOVZXURTCKPRDQ-CQSZACIVSA-N n-[4-[chloro(difluoro)methoxy]phenyl]-6-[(3r)-3-hydroxypyrrolidin-1-yl]-5-(1h-pyrazol-5-yl)pyridine-3-carboxamide Chemical compound C1[C@H](O)CCN1C1=NC=C(C(=O)NC=2C=CC(OC(F)(F)Cl)=CC=2)C=C1C1=CC=NN1 VOVZXURTCKPRDQ-CQSZACIVSA-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
- 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
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 230000001007 puffing effect Effects 0.000 description 1
- 239000000523 sample Substances 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
- 229940029284 trichlorofluoromethane Drugs 0.000 description 1
- 229930195735 unsaturated hydrocarbon Natural products 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
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
- Y10S131/901—Organic liquid employed in puffing tobacco
Definitions
- Tobacco is impregnated with a volatile organic liquid and then heated by rapidly passing a stream of hot gas in contact therewith to volatilize the liquid and expand the tobacco.
- the hot tobacco contacting gas is at a temperature at least 30 F. above the boiling point of the said liquid.
- PROCESS FOR INCREASING TI-IE 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.
- 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.
- an object of this invention is to provide a process for increasing the filling capacity of tobacco to an extent not heretofore readily obtainable.
- a further object of this invention is the provision of a process for increasing the filling capacity of tobacco which avoids the shattering of the tobacco particles and the attendant formation of fines.
- a further object of this invention is the provision of a process for expanding tobacco which may be readily carried out on conventional commercial equipment without the necessity of using high pressure.
- An additional object of this invention is the provision of a process for increasing the filling capacity of tobacco which is broadly applicable to the treatment of leaf, strips, cut filler,
- a cured tobacco product in the form of cut filler, leaf, strips, stems, veins or reconstituted tobacco is contacted with a sufficient quantity of a volatile organic liquid to thoroughly impregnate it.
- the tobacco is allowed to remain in contact with the volatile liquid, i.e., equilibrated, for a time sufficient for thorough impregnation to occur.
- the impregnated tobacco is brought into contact with a stream of gas which has been heated to an elevated temperature substantially above the boiling point of the volatile organic liquid whereby the liquid is rapidly volatilized and then separated from the tobacco by the gaseous stream in the form of a vapor.
- the moisture content of the resulting tobacco may then be further adjusted to the original level by conventional procedures.
- the bulk density of the final tobacco product is significantly less than that of the starting tobacco whereby its filling capacity is substantially increased.
- the entire process is readily carried out at atmospheric pressure.
- the hot gas used for vaporizing and removing the volatile liquid from the tobacco in the vapor state is preferably heated to a temperature at least F. higher than the boiling point of the volatile organic liquid under the pressures obtained during heating in order to effect the desired expansion and rapid removal of liquid.
- the process of this 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. lf the entire blend is to be treated, then cut filler is preferably utilized.
- the volatile organic liquids that may be used for impregnating tobacco in accordance with this invention preferably are those which are chemically inert to the tobacco being treated and unreactive toward the hot gas that comes into contact therewith during the vaporization step.
- the organic liquid may be miscible or wholly or partially immiscible with water and may be selected from a number of the well-known organic liquids that are available to the industry. As indicated, the liquid should be readily volatile, without leaving a residue, and have a boiling point under prevailing pressures at least 30 F. lower than the temperature of the hot gas used to treat the impregnated tobacco so that the tobacco particles are properly expanded and the liquid is rapidly removed in the vapor state.
- Illustrative suitable inert organic liquids are: aromatic hydrocarbons such as benzene and toluene; ketones such as acetone, methyl ethyl ketone, methyl isopropyl ketone, diethyl ketone and diacetyl; aliphatic or cyclic ethers such as methyl ethyl ether, diethyl ether, dipropyl ether, diisopropyl ether, methyl butyl ether, ethyl butyl ether, ethylene glycol dimethyl ether, and tetrahydrofuran; aliphatic alcohols such as methanol, ethanol, propanol, 2-propanol, sec-butyl alcohol, t-butyl alcohol, t-amyl alcohol, and allyl alcohol; aliphatic hydrocarbons such as butane, pentane, hexane, heptane, and the corresponding unsaturated hydrocarbons;
- Preferred classes of liquids are those not miscible with water in all proportions such as aliphatic hydrocarbons having 3 to 6 carbon atoms and the halogen substituted alkane hydrocarbons having 1-2 carbon atoms and the halocycloalkanes having 34 carbon atoms.
- the amount of volatile organic liquid used to impregnate the tobacco will depend upon a number of factors such as the physical state of the tobacco being treated, the particular organic liquid used and the degree of impregnation desired. Generally speaking, the amount of liquid used is that which will thoroughly impregnate the tobacco without leaving any substantial excess of liquid which can be separated and drained away from the body of tobacco treated. Generally speaking, the amount of liquid used to achieve such impregnation will range between about one-third to about three times the amount of tobacco treated on a weight basis. Expressed in another way,.the weight ratio of liquid to tobacco may be between l-to-3 and 3,-to-l.
- the tobacco be allowed to equilibrate, i.e., remain in contact, with the liquid for a period of time.
- this time will depend upon the physical state of the tobacco and the particular liquid that may be selected for impregnation.
- the contact time may be longer than for the treatment of more finely divided tobacco particles such as cut 'filler. Periods from a few minutes to as long as 24 hours are satisfactory.
- a feature of the invention is that no special equipment is required for subjecting the tobacco to the initial impregnation step and it may be carried out in any suitable type of tank,
- the equilibration should be carried out at reduced temperatures or elevated pressures so that the liquid does not vaporize or escape during the equilibration step.
- a hot gas is passed through the tobacco in order to rapidly vaporize the liquid.
- the hot gas is preferably steam but may be any other gas which is inert to the tobacco and the volatile liquid.
- the temperature of the gas is preferably 30 F. above the boiling point of the organic liquid and it is rapidly passed through the body of the impregnated tobacco in order to effect rapid vaporization of the liquid from the tobacco. This causes expansion without concomitant fragmentation of the tobacco particles.
- This step in the process is also preferably carried out under ordinary pressures and in any convenient type of equipment.
- the hot gas is passed through the tobacco until substantially all of the volatile liquid has been vaporized and then driven off in the form of a vapor.
- steam at about 212 F. may be used.
- the temperature of the hot gas can be higher (e.g., superheated steam). Gas temperatures above about 400 F. should be avoided since they may adversely affect the flavor and aroma of the tobacco being treated.
- This tobacco product having decreased bulk density, is particularly useful for the manufacture of smoking products such as cigarettes, cigars and pipe tobacco.
- the bulk density having been decreased, considerable savings in tobacco cost are obtained in the manufacture of these smoking products without sacrificing quality.
- 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 ofa given weight of tobacco, 100 grams, is determined. Experiments have shown that this apparatus will accurately determine the volume (filling capacity) of a given amount of cut tobacco with good reproducibility.
- the pressure on the tobacco applied by the piston in all examples was 2.30 pounds per square inch applied for five seconds, at which time the volume reading was taken. This pressure corresponds closely to the pressure normally applied by the wrapping paper to tobacco in cigarettes.
- the moisture content of the tobacco affects the filling capacity values determined by this method, therefore comparative filling capacities were obtained at similar moisture contents.
- EXAMPLE A cured cut cigarette tobacco containing 12.3 percent moisture and having a' filling capacity of 458 milliliters when determined by the procedure previously indicated was mixed with a sufficient amount of ethanol (boiling point about 173 F.) to thoroughly impregnate the tobacco.
- the alcoholtreated tobacco was equilibrated in a closed container for about 20 hours, after which time a stream of steam having a temperature of 212 F. was passed through the alcohol-treated tobacco for a period of five minutes. After this time the tobacco had expanded and the alcohol had been completely removed by vaporization. The moisture content of the tobac co was then adjusted to 10.9 percent.
- the resulting tobacco was suitable for use in the manufacture of cigarettes and had a filling capacity of 517 milliliters, which represents an increase of approximately 12.9 percent over the original tobacco.
- Example 2 The procedure of Example 1 was repeated except that acetone (B.P., about 134 F.) was used as the volatile organic liquid and the treated tobacco was steamed for three minutes with the final moisture content being adjusted to 1 1.1 percent.
- the filling capacity was 533 milliliters, representing an increase of approximately 19.7 percent over the untreated tobacco.
- EXAMPLE 3 The process of Example 1 was repeated except that ethyl ether (B.P., about 94.2 F.) was used as the liquid, the steaming was carried out for two minutes, and the moisture content of the final tobacco was adjusted to 9.7 percent.
- the filling capacity of the tobacco product was 614 milliliters, representing an increase of approximately 34.1 percent.
- EXAMPLE 4 The process of Example 1 was repeated except that the organic liquid was benzene (B.P., about 176 F.) and the treated tobacco was steamed for five minutes and the moisture content of the final product was adjusted to 12.0 percent. The filling capacity of the product was 522 milliliters, representing an increase of approximately 14.0 percent.
- Example 1 The process of Example 1 was repeated using hexane (B.P., about 156 F.) as the organic liquid, steaming for five minutes and adjusting the moisture content of the final product to 12.1 percent.
- the filling capacity was 576 milliliters, representing an increase of approximately 25.8 percent.
- Example 6 The process of Example 1 was repeated except that pentane (B.P., about F.) was the organic liquid, the product was steamed for two minutes, and the moisture content of the final tobacco was adjusted to 12.1 percent.
- the filling capacity was 704 milliliters, representing an increase of approximately 53.7 percent.
- Example 7 The process of Example 6 was repeated except that the steaming was carried out for only one minute and the moisture content was adjusted to 9.6 percent.
- the filling capacity of the final tobacco was 921 milliliters, representing an increase of approximately 101.0 percent.
- Example 8 The process of Example 1 was repeated utilizing dichloromethane (B.P., about 104 F.) as the liquid and steaming for 75 seconds, with final moisture readjustment to 10.0 percent.
- the filling capacity of the product was 605 milliliters, corresponding to an increase of approximately 32.2 percent.
- Example 9 The process of Example 1 was repeated employing Freon- 1 1 (trichloromonofluoromethanc, B.P., about 75 F.) as the organic liquid.
- Freon- 1 1 trichloromonofluoromethanc, B.P., about 75 F.
- the mixture of tobacco and Freon-11 was stored under slight superatmospheric pressure to prevent vaporization during the equilibration process. After storage, steaming was effected for two minutes and the moisture in the final product was adjusted to 10.1 percent.
- the filling capacity of the final tobacco was 682 milliliters, representing an increase of approximately 46.8 percent.
- EXAMPLE I0 Shredded flue-cured tobacco stems (200 grams) were treated with 250 milliliters of pentane and equilibrated overnight in a closed container. The treated tobacco was then exposed to steam at 212 F. for a period of one minute and dried in air. The moisture content of the resulting tobacco was 13.5 percent and its filling capacity was 921 milliliters. A control sample which had not been treated with the pentane had a moisture content of 14.0 and a filling capacity of 466 milliliters. Thus, the filling capacity due to the pentane treatment followed by steaming was increased approximately 98.6 percent.
- Example II The experiment of Example was repeated except that ethyl ether was used as the organic liquid.
- the moisture content of the final tobacco was 14.0 percent and the filling capacity was 563 milliliters, representing an increase of approximately 21 percent over the control.
- EXAMPLE 12 The experiment of Example 10 was repeated using shredded burley tobacco stems with pentane as the organic liquid. The final product had a moisture content of 12.5 percent and a filling capacity of 1036 milliliters. The control which had not been subjected to pentane had a moisture content of 12.6 percent and a filling capacity of 743 milliliters. Thus, the pentanetreated and steamed sample showed an increase in filling capacity over the control of approximately 39.4 percent.
- Example 13 The process of Example 12 was repeated using shredded burley tobacco stems and ethyl ether as the organic liquid. The final moisture content was 13.1 percent and the filling capacity was 821 milliliters, representing a 10.5 percent increase over the control.
- steam has been indicated in the foregoing examples as the hot gas for volatilizing the liquid in the moistened tobacco, it will be readily apparent that otherheated gases such as nitrogen, carbon dioxide, methane, etc., which are inert to the tobacco and to the liquid may be employed. Also, if desired, superheated steam may be employed to advantage to effect a more rapid vaporization and removal of the organic liquid, particularly those having higher boiling points.
- a process for increasing the filling capacity of tobacco which comprises contacting tobacco with a sufficient quantity of a volatile organic liquid to impregnate same, thereafter without substantially increasing the pressure rapidly passing a gas into contact with said impregnated tobacco, said gas being heated to a temperature of at least 30 F. above the boiling point of said liquid at the gas contacting pressure, whereby said liquid in the tobacco is essentially completely and rapidly vaporized within said tobacco and said tobacco is expanded and separating the vaporized liquid from the tobacco in the vapor state.
- a process for increasing the filling capacity of tobacco which comprises admixing tobacco with a volatile organic liquid, the amount of liquid being sufficient to wet the tobacco, equilibrating the mixture to permit the liquid to substantially completely impregnate the tobacco particles, rapidly passing a stream of gas through the tobacco while still wet with said liquid, said gas having a temperature at least 30 F. above the boiling point of said liquid at the pressure at which the gas is passed through the tobacco, whereby the liquid is rapidly removed therefrom in the vapor state and the tobacco is expanded and separating the vaporized liquid from the tobacco.
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- Manufacture Of Tobacco Products (AREA)
Description
United States Patent Inventor Appl. No. Filed Patented Assignee PROCESS FOR INCREASING THE FILLING CAPACITY OF TOBACCO 8 Claims, No Drawings U.S. Cl 131/140 Int. Cl A24b 3/18 Field of Search 131/143,
References Cited UNITED STATES PATENTS 8/1956 Baer Baer l3l/l40UX 283,622 8/1883 Lierreich et a1 13 l/143UX 1,577,768 3/1926 Smith 131/143 2,117,558 5/1938 Hyatt 131/143X 2,227,863 1/1941 Rhodes 131/143 3,223,090 12/1965 Strubel et al 131/140 FOREIGN PATENTS 646,439 8/1962 Canada 131/143 OTHER REFERENCES A.P.C. application of Boehme et a1., Ser. No. 304,214, published May 11, 1943 (aband) Primary Examiner-Melvin D. Rein Attorney-Pendleton, Neuman, Williams & Anderson ABSTRACT: Tobacco is impregnated with a volatile organic liquid and then heated by rapidly passing a stream of hot gas in contact therewith to volatilize the liquid and expand the tobacco. The hot tobacco contacting gas is at a temperature at least 30 F. above the boiling point of the said liquid.
PROCESS FOR INCREASING TI-IE 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.
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.
Accordingly, an object of this invention is to provide a process for increasing the filling capacity of tobacco to an extent not heretofore readily obtainable.
A further object of this invention is the provision of a process for increasing the filling capacity of tobacco which avoids the shattering of the tobacco particles and the attendant formation of fines.
A further object of this invention is the provision of a process for expanding tobacco which may be readily carried out on conventional commercial equipment without the necessity of using high pressure.
An additional object of this invention is the provision of a process for increasing the filling capacity of tobacco which is broadly applicable to the treatment of leaf, strips, cut filler,
stems or veins.
Further additional objects will appear from the following description and the accompanying claims.
In accordance with one embodiment of this invention, a cured tobacco product in the form of cut filler, leaf, strips, stems, veins or reconstituted tobacco is contacted with a sufficient quantity of a volatile organic liquid to thoroughly impregnate it. The tobacco is allowed to remain in contact with the volatile liquid, i.e., equilibrated, for a time sufficient for thorough impregnation to occur. Thereafter, the impregnated tobacco is brought into contact with a stream of gas which has been heated to an elevated temperature substantially above the boiling point of the volatile organic liquid whereby the liquid is rapidly volatilized and then separated from the tobacco by the gaseous stream in the form of a vapor. The moisture content of the resulting tobacco may then be further adjusted to the original level by conventional procedures. The bulk density of the final tobacco product is significantly less than that of the starting tobacco whereby its filling capacity is substantially increased. The entire process is readily carried out at atmospheric pressure. The hot gas used for vaporizing and removing the volatile liquid from the tobacco in the vapor state is preferably heated to a temperature at least F. higher than the boiling point of the volatile organic liquid under the pressures obtained during heating in order to effect the desired expansion and rapid removal of liquid.
The process of this 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. lf the entire blend is to be treated, then cut filler is preferably utilized.
The volatile organic liquids that may be used for impregnating tobacco in accordance with this invention preferably are those which are chemically inert to the tobacco being treated and unreactive toward the hot gas that comes into contact therewith during the vaporization step. The organic liquid may be miscible or wholly or partially immiscible with water and may be selected from a number of the well-known organic liquids that are available to the industry. As indicated, the liquid should be readily volatile, without leaving a residue, and have a boiling point under prevailing pressures at least 30 F. lower than the temperature of the hot gas used to treat the impregnated tobacco so that the tobacco particles are properly expanded and the liquid is rapidly removed in the vapor state.
Illustrative suitable inert organic liquids are: aromatic hydrocarbons such as benzene and toluene; ketones such as acetone, methyl ethyl ketone, methyl isopropyl ketone, diethyl ketone and diacetyl; aliphatic or cyclic ethers such as methyl ethyl ether, diethyl ether, dipropyl ether, diisopropyl ether, methyl butyl ether, ethyl butyl ether, ethylene glycol dimethyl ether, and tetrahydrofuran; aliphatic alcohols such as methanol, ethanol, propanol, 2-propanol, sec-butyl alcohol, t-butyl alcohol, t-amyl alcohol, and allyl alcohol; aliphatic hydrocarbons such as butane, pentane, hexane, heptane, and the corresponding unsaturated hydrocarbons; the cyclo aliphatic hydrocarbons such as cyclobutane, cyclopentane, cyclohexane and cyclohexene; the halo-hydrocarbons 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, flourobenzene, and the Freon liquids represented by trichloromonofluoromethane, dichlorodifluoromethane, monobromotrifluoromethane, monochlorodifluoromethane, trichlorotrifluoroethane, dichlorotetrafluoroethane, v octafluorocyclobutane, and tetrachlorodifluoroethane.
Preferred classes of liquids are those not miscible with water in all proportions such as aliphatic hydrocarbons having 3 to 6 carbon atoms and the halogen substituted alkane hydrocarbons having 1-2 carbon atoms and the halocycloalkanes having 34 carbon atoms.
The amount of volatile organic liquid used to impregnate the tobacco will depend upon a number of factors such as the physical state of the tobacco being treated, the particular organic liquid used and the degree of impregnation desired. Generally speaking, the amount of liquid used is that which will thoroughly impregnate the tobacco without leaving any substantial excess of liquid which can be separated and drained away from the body of tobacco treated. Generally speaking, the amount of liquid used to achieve such impregnation will range between about one-third to about three times the amount of tobacco treated on a weight basis. Expressed in another way,.the weight ratio of liquid to tobacco may be between l-to-3 and 3,-to-l.
After the tobacco has been impregnated with the organic liquid, it is preferred that, the tobacco be allowed to equilibrate, i.e., remain in contact, with the liquid for a period of time. Here again this time will depend upon the physical state of the tobacco and the particular liquid that may be selected for impregnation. In the case of leaf, stems or strips, the contact time may be longer than for the treatment of more finely divided tobacco particles such as cut 'filler. Periods from a few minutes to as long as 24 hours are satisfactory.
The temperature and pressure conditions under which the tobacco is contacted with the organic liquid do not appear'to be critical, and generally speaking, ordinary room temperatures and pressures are entirely satisfactory. As a matter of fact, a feature of the invention is that no special equipment is required for subjecting the tobacco to the initial impregnation step and it may be carried out in any suitable type of tank,
drum or other container. However, in the case ofliquids having a low boiling point or high vapor pressure, the equilibration should be carried out at reduced temperatures or elevated pressures so that the liquid does not vaporize or escape during the equilibration step.
After the tobacco has become thoroughly impregnated with the organic liquid, a hot gas is passed through the tobacco in order to rapidly vaporize the liquid. The hot gas is preferably steam but may be any other gas which is inert to the tobacco and the volatile liquid. As previously indicated, the temperature of the gas is preferably 30 F. above the boiling point of the organic liquid and it is rapidly passed through the body of the impregnated tobacco in order to effect rapid vaporization of the liquid from the tobacco. This causes expansion without concomitant fragmentation of the tobacco particles. This step in the process is also preferably carried out under ordinary pressures and in any convenient type of equipment. The hot gas is passed through the tobacco until substantially all of the volatile liquid has been vaporized and then driven off in the form of a vapor. Where low boiling liquids such as pentane or Freon-l1 are used, steam at about 212 F. may be used. With the high boiling liquids the temperature of the hot gas can be higher (e.g., superheated steam). Gas temperatures above about 400 F. should be avoided since they may adversely affect the flavor and aroma of the tobacco being treated.
By the process of this invention it is possible to increase the filling capacity of cured tobacco by as much as to 100 percent or even more. This tobacco product, having decreased bulk density, is particularly useful for the manufacture of smoking products such as cigarettes, cigars and pipe tobacco. The bulk density having been decreased, considerable savings in tobacco cost are obtained in the manufacture of these smoking products without sacrificing quality.
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 ofa given weight of tobacco, 100 grams, is determined. Experiments have shown that this apparatus will accurately determine the volume (filling capacity) of a given amount of cut tobacco with good reproducibility. The pressure on the tobacco applied by the piston in all examples was 2.30 pounds per square inch applied for five seconds, at which time the volume reading was taken. This pressure corresponds closely to the pressure normally applied by the wrapping paper to tobacco in cigarettes. The moisture content of the tobacco affects the filling capacity values determined by this method, therefore comparative filling capacities were obtained at similar moisture contents.
For a more complete understanding of this invention, reference will now be made to several examples which are illustrative thereof:
EXAMPLE] A cured cut cigarette tobacco containing 12.3 percent moisture and having a' filling capacity of 458 milliliters when determined by the procedure previously indicated was mixed with a sufficient amount of ethanol (boiling point about 173 F.) to thoroughly impregnate the tobacco. The alcoholtreated tobacco was equilibrated in a closed container for about 20 hours, after which time a stream of steam having a temperature of 212 F. was passed through the alcohol-treated tobacco for a period of five minutes. After this time the tobacco had expanded and the alcohol had been completely removed by vaporization. The moisture content of the tobac co was then adjusted to 10.9 percent. The resulting tobacco was suitable for use in the manufacture of cigarettes and had a filling capacity of 517 milliliters, which represents an increase of approximately 12.9 percent over the original tobacco.
EXAMPLE 2 The procedure of Example 1 was repeated except that acetone (B.P., about 134 F.) was used as the volatile organic liquid and the treated tobacco was steamed for three minutes with the final moisture content being adjusted to 1 1.1 percent. The filling capacity was 533 milliliters, representing an increase of approximately 19.7 percent over the untreated tobacco.
EXAMPLE 3 The process of Example 1 was repeated except that ethyl ether (B.P., about 94.2 F.) was used as the liquid, the steaming was carried out for two minutes, and the moisture content of the final tobacco was adjusted to 9.7 percent. The filling capacity of the tobacco product was 614 milliliters, representing an increase of approximately 34.1 percent.
EXAMPLE 4 The process of Example 1 was repeated except that the organic liquid was benzene (B.P., about 176 F.) and the treated tobacco was steamed for five minutes and the moisture content of the final product was adjusted to 12.0 percent. The filling capacity of the product was 522 milliliters, representing an increase of approximately 14.0 percent.
EXAMPLES The process of Example 1 was repeated using hexane (B.P., about 156 F.) as the organic liquid, steaming for five minutes and adjusting the moisture content of the final product to 12.1 percent. The filling capacity was 576 milliliters, representing an increase of approximately 25.8 percent.
EXAMPLE 6 The process of Example 1 was repeated except that pentane (B.P., about F.) was the organic liquid, the product was steamed for two minutes, and the moisture content of the final tobacco was adjusted to 12.1 percent. The filling capacity was 704 milliliters, representing an increase of approximately 53.7 percent.
EXAMPLE7 The process of Example 6 was repeated except that the steaming was carried out for only one minute and the moisture content was adjusted to 9.6 percent. The filling capacity of the final tobacco was 921 milliliters, representing an increase of approximately 101.0 percent.
EXAMPLE 8 The process of Example 1 was repeated utilizing dichloromethane (B.P., about 104 F.) as the liquid and steaming for 75 seconds, with final moisture readjustment to 10.0 percent. The filling capacity of the product was 605 milliliters, corresponding to an increase of approximately 32.2 percent.
EXAMPLE9 The process of Example 1 was repeated employing Freon- 1 1 (trichloromonofluoromethanc, B.P., about 75 F.) as the organic liquid. The mixture of tobacco and Freon-11 was stored under slight superatmospheric pressure to prevent vaporization during the equilibration process. After storage, steaming was effected for two minutes and the moisture in the final product was adjusted to 10.1 percent. The filling capacity of the final tobacco was 682 milliliters, representing an increase of approximately 46.8 percent.
EXAMPLE I0 Shredded flue-cured tobacco stems (200 grams) were treated with 250 milliliters of pentane and equilibrated overnight in a closed container. The treated tobacco was then exposed to steam at 212 F. for a period of one minute and dried in air. The moisture content of the resulting tobacco was 13.5 percent and its filling capacity was 921 milliliters. A control sample which had not been treated with the pentane had a moisture content of 14.0 and a filling capacity of 466 milliliters. Thus, the filling capacity due to the pentane treatment followed by steaming was increased approximately 98.6 percent.
EXAMPLEII The experiment of Example was repeated except that ethyl ether was used as the organic liquid. The moisture content of the final tobacco was 14.0 percent and the filling capacity was 563 milliliters, representing an increase of approximately 21 percent over the control.
EXAMPLE 12 The experiment of Example 10 was repeated using shredded burley tobacco stems with pentane as the organic liquid. The final product had a moisture content of 12.5 percent and a filling capacity of 1036 milliliters. The control which had not been subjected to pentane had a moisture content of 12.6 percent and a filling capacity of 743 milliliters. Thus, the pentanetreated and steamed sample showed an increase in filling capacity over the control of approximately 39.4 percent.
EXAMPLE 13 The process of Example 12 was repeated using shredded burley tobacco stems and ethyl ether as the organic liquid. The final moisture content was 13.1 percent and the filling capacity was 821 milliliters, representing a 10.5 percent increase over the control.
EXAMPLE [4 the following table:
! Data based on average of 50 cigarettes (70 mm.). 2 Cigarettes stored at 63% humidity for 94 hours.
While steam has been indicated in the foregoing examples as the hot gas for volatilizing the liquid in the moistened tobacco, it will be readily apparent that otherheated gases such as nitrogen, carbon dioxide, methane, etc., which are inert to the tobacco and to the liquid may be employed. Also, if desired, superheated steam may be employed to advantage to effect a more rapid vaporization and removal of the organic liquid, particularly those having higher boiling points.
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.
lclaim: 1. A process for increasing the filling capacity of tobacco which comprises contacting tobacco with a sufficient quantity of a volatile organic liquid to impregnate same, thereafter without substantially increasing the pressure rapidly passing a gas into contact with said impregnated tobacco, said gas being heated to a temperature of at least 30 F. above the boiling point of said liquid at the gas contacting pressure, whereby said liquid in the tobacco is essentially completely and rapidly vaporized within said tobacco and said tobacco is expanded and separating the vaporized liquid from the tobacco in the vapor state.
2. The process of claim 1 in which said gas is steam.
3. The process of claim 1 in which the weight ratio of liquid to tobacco in the gas contacting step is between about 3 to l and l to 3.
4. The process of claim 1 in which the liquid is a halogenated hydrocarbon.
5. The process of claim 1 in which the liquid is a fluorohydrocarbon.
6. The process of claim 1 in which the liquid is a hydrocarbon.
7. A process for increasing the filling capacity of tobacco which comprises admixing tobacco with a volatile organic liquid, the amount of liquid being sufficient to wet the tobacco, equilibrating the mixture to permit the liquid to substantially completely impregnate the tobacco particles, rapidly passing a stream of gas through the tobacco while still wet with said liquid, said gas having a temperature at least 30 F. above the boiling point of said liquid at the pressure at which the gas is passed through the tobacco, whereby the liquid is rapidly removed therefrom in the vapor state and the tobacco is expanded and separating the vaporized liquid from the tobacco.
8. The process of claim 1 in which the organic liquid is trichloromonofiuoromethane.
Priority Applications (15)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US720406A US3524451A (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 |
| DE19691917552 DE1917552C3 (en) | 1968-04-10 | 1969-04-01 | Process for increasing the filling capacity of tobacco |
| NO1375/69A NO122519B (en) | 1968-04-10 | 1969-04-01 | |
| 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 |
|---|---|---|---|
| US720406A US3524451A (en) | 1968-04-10 | 1968-04-10 | Process for increasing the filling capacity of tobacco |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US05/558,674 Reissue USRE30693E (en) | 1975-03-17 | 1975-03-17 | Process for increasing the filling capacity of tobacco |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3524451A true US3524451A (en) | 1970-08-18 |
Family
ID=24893914
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US720406A Expired - Lifetime US3524451A (en) | 1968-04-10 | 1968-04-10 | Process for increasing the filling capacity of tobacco |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US3524451A (en) |
Cited By (29)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3683937A (en) * | 1970-12-24 | 1972-08-15 | Reynolds Leasing Corp | Tobacco expansion process |
| US3693631A (en) * | 1971-04-28 | 1972-09-26 | Reynolds Leasing Corp | Tobacco expansion process |
| US3753440A (en) * | 1972-03-07 | 1973-08-21 | Reynolds Tobacco Co R | Tobacco expansion process |
| US3771533A (en) * | 1970-08-31 | 1973-11-13 | Philip Morris Inc | Process for puffing tobacco |
| DE2503636A1 (en) * | 1974-02-05 | 1975-08-14 | Airco Inc | METHOD AND DEVICE FOR EXTENDING ORGANIC SUBSTANCES |
| DE2515561A1 (en) * | 1974-04-15 | 1975-10-30 | Reynolds Tobacco Co R | SMOKE MATERIAL |
| 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 |
| DE2903300A1 (en) * | 1979-01-29 | 1980-07-31 | Reemtsma H F & Ph | METHOD FOR IMPROVING THE FILLABILITY OF 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 |
| US4821747A (en) * | 1986-04-23 | 1989-04-18 | R. J. Reynolds Tobacco Company | Process for treating tobacco and similar organic materials |
| US4870980A (en) * | 1987-04-10 | 1989-10-03 | R. J. Reynolds Tobacco Company | Tobacco expansion process and apparatus |
| US4924888A (en) * | 1987-05-15 | 1990-05-15 | R. J. Reynolds Tobacco Company | Smoking article |
| US4962773A (en) * | 1987-08-13 | 1990-10-16 | R. J. Reynolds Tobacco Company | Process for the manufacture tobacco rods containing expanded tobacco material |
| US5012826A (en) * | 1989-08-04 | 1991-05-07 | R. I. Reynolds Tobacco Company | Method of expanding tobacco |
| US5031644A (en) * | 1989-12-29 | 1991-07-16 | R. J. Reynolds Tobacco Company | Tobacco expansion process and product |
| US5037663A (en) * | 1981-10-14 | 1991-08-06 | Colorado State University Research Foundation | Process for increasing the reactivity of cellulose-containing materials |
| 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 |
| US5590667A (en) * | 1995-07-28 | 1997-01-07 | Scw, Inc. | Tobacco expansion method |
| 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 |
| CN104799433A (en) * | 2015-02-16 | 2015-07-29 | 广东省金叶科技开发有限公司 | Method for treating tea stems to prepare filter stick flavor increasing particles by microwave expansion technology |
| WO2020001496A1 (en) * | 2018-06-26 | 2020-01-02 | 中国科学院理化技术研究所 | Efficient preparation method for expanded shag |
| CN110638084A (en) * | 2018-06-26 | 2020-01-03 | 中国科学院理化技术研究所 | A low-carbon and environmentally friendly low-temperature expansion process for cut tobacco |
| US20210161197A1 (en) * | 2019-06-27 | 2021-06-03 | China Tobacco Guangdong Industrial Co., Ltd. | Heat-not-burn tobacco matrix for preventing cut tobacco from falling and application thereof |
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1968
- 1968-04-10 US US720406A patent/US3524451A/en not_active Expired - Lifetime
Cited By (34)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3771533A (en) * | 1970-08-31 | 1973-11-13 | Philip Morris Inc | Process for puffing tobacco |
| US3683937A (en) * | 1970-12-24 | 1972-08-15 | Reynolds Leasing Corp | Tobacco expansion process |
| US3693631A (en) * | 1971-04-28 | 1972-09-26 | Reynolds Leasing Corp | Tobacco expansion process |
| US3753440A (en) * | 1972-03-07 | 1973-08-21 | Reynolds Tobacco Co R | Tobacco expansion process |
| DE2503636A1 (en) * | 1974-02-05 | 1975-08-14 | Airco Inc | METHOD AND DEVICE FOR EXTENDING ORGANIC SUBSTANCES |
| DE2515561A1 (en) * | 1974-04-15 | 1975-10-30 | Reynolds Tobacco Co R | SMOKE MATERIAL |
| 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 |
| DE2903300A1 (en) * | 1979-01-29 | 1980-07-31 | Reemtsma H F & Ph | METHOD FOR IMPROVING THE FILLABILITY OF TOBACCO |
| US4388932A (en) * | 1980-12-31 | 1983-06-21 | Philip Morris, Incorporated | Process for improving filling power of expanded tobacco |
| US5037663A (en) * | 1981-10-14 | 1991-08-06 | Colorado State University Research Foundation | Process for increasing the reactivity of cellulose-containing materials |
| 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 |
| US4870980A (en) * | 1987-04-10 | 1989-10-03 | R. J. Reynolds Tobacco Company | Tobacco expansion process and apparatus |
| US4924888A (en) * | 1987-05-15 | 1990-05-15 | R. J. Reynolds Tobacco Company | Smoking article |
| US4962773A (en) * | 1987-08-13 | 1990-10-16 | R. J. Reynolds Tobacco Company | Process for the manufacture tobacco rods containing expanded tobacco material |
| US5076293A (en) * | 1989-06-19 | 1991-12-31 | R. J. Reynolds Tobacco Company | Process and apparatus for the treatment of tobacco material |
| US5012826A (en) * | 1989-08-04 | 1991-05-07 | R. I. Reynolds Tobacco Company | Method of expanding tobacco |
| 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 |
| US5590667A (en) * | 1995-07-28 | 1997-01-07 | Scw, Inc. | Tobacco expansion method |
| 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 |
| CN104799433A (en) * | 2015-02-16 | 2015-07-29 | 广东省金叶科技开发有限公司 | Method for treating tea stems to prepare filter stick flavor increasing particles by microwave expansion technology |
| CN104799433B (en) * | 2015-02-16 | 2018-11-23 | 广东省金叶科技开发有限公司 | A method of filter stick perfumed granules are prepared using microwave expansion technical treatment tea stalk |
| WO2020001496A1 (en) * | 2018-06-26 | 2020-01-02 | 中国科学院理化技术研究所 | Efficient preparation method for expanded shag |
| CN110638083A (en) * | 2018-06-26 | 2020-01-03 | 中国科学院理化技术研究所 | Efficient preparation method of expanded cut tobacco |
| CN110638084A (en) * | 2018-06-26 | 2020-01-03 | 中国科学院理化技术研究所 | A low-carbon and environmentally friendly low-temperature expansion process for cut tobacco |
| CN110638083B (en) * | 2018-06-26 | 2021-12-07 | 中国科学院理化技术研究所 | Efficient preparation method of expanded cut tobacco |
| US20210161197A1 (en) * | 2019-06-27 | 2021-06-03 | China Tobacco Guangdong Industrial Co., Ltd. | Heat-not-burn tobacco matrix for preventing cut tobacco from falling and application thereof |
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