US3126011A - Tobacco composition and smoking unit - Google Patents
Tobacco composition and smoking unit Download PDFInfo
- Publication number
- US3126011A US3126011A US3126011DA US3126011A US 3126011 A US3126011 A US 3126011A US 3126011D A US3126011D A US 3126011DA US 3126011 A US3126011 A US 3126011A
- Authority
- US
- United States
- Prior art keywords
- tobacco
- smoking
- cigarette
- solid
- sodium
- 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
- 235000002637 Nicotiana tabacum Nutrition 0.000 title claims description 52
- 239000000203 mixture Substances 0.000 title claims description 26
- 230000000391 smoking effect Effects 0.000 title claims description 18
- 244000061176 Nicotiana tabacum Species 0.000 title 1
- 241000208125 Nicotiana Species 0.000 claims description 51
- 239000007787 solid Substances 0.000 claims description 24
- 239000002245 particle Substances 0.000 claims description 17
- 238000002844 melting Methods 0.000 claims description 13
- 230000008018 melting Effects 0.000 claims description 13
- -1 ALKALI METAL SALT Chemical class 0.000 claims description 5
- 229910019142 PO4 Inorganic materials 0.000 claims description 5
- 150000001642 boronic acid derivatives Chemical class 0.000 claims description 4
- 150000004760 silicates Chemical class 0.000 claims description 4
- 239000002253 acid Substances 0.000 claims description 3
- 229910052783 alkali metal Inorganic materials 0.000 claims description 3
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims description 2
- 235000019504 cigarettes Nutrition 0.000 description 14
- 150000003839 salts Chemical class 0.000 description 11
- 239000000779 smoke Substances 0.000 description 8
- 230000000711 cancerogenic effect Effects 0.000 description 6
- 231100000315 carcinogenic Toxicity 0.000 description 6
- 229910052500 inorganic mineral Inorganic materials 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 239000011707 mineral Substances 0.000 description 5
- 235000010755 mineral Nutrition 0.000 description 5
- 239000000654 additive Substances 0.000 description 4
- 239000000470 constituent Substances 0.000 description 4
- 230000002939 deleterious effect Effects 0.000 description 4
- PYUBPZNJWXUSID-UHFFFAOYSA-N pentadecapotassium;pentaborate Chemical compound [K+].[K+].[K+].[K+].[K+].[K+].[K+].[K+].[K+].[K+].[K+].[K+].[K+].[K+].[K+].[O-]B([O-])[O-].[O-]B([O-])[O-].[O-]B([O-])[O-].[O-]B([O-])[O-].[O-]B([O-])[O-] PYUBPZNJWXUSID-UHFFFAOYSA-N 0.000 description 4
- 235000021317 phosphate Nutrition 0.000 description 4
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 4
- 241000894007 species Species 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 239000011269 tar Substances 0.000 description 4
- MOMKYJPSVWEWPM-UHFFFAOYSA-N 4-(chloromethyl)-2-(4-methylphenyl)-1,3-thiazole Chemical compound C1=CC(C)=CC=C1C1=NC(CCl)=CS1 MOMKYJPSVWEWPM-UHFFFAOYSA-N 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 231100000357 carcinogen Toxicity 0.000 description 3
- 239000003183 carcinogenic agent Substances 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 238000002485 combustion reaction Methods 0.000 description 3
- JKWMSGQKBLHBQQ-UHFFFAOYSA-N diboron trioxide Chemical compound O=BOB=O JKWMSGQKBLHBQQ-UHFFFAOYSA-N 0.000 description 3
- 150000004677 hydrates Chemical class 0.000 description 3
- 230000001473 noxious effect Effects 0.000 description 3
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 3
- NVIFVTYDZMXWGX-UHFFFAOYSA-N sodium metaborate Chemical compound [Na+].[O-]B=O NVIFVTYDZMXWGX-UHFFFAOYSA-N 0.000 description 3
- 235000019983 sodium metaphosphate Nutrition 0.000 description 3
- 229910011255 B2O3 Inorganic materials 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- WDECIBYCCFPHNR-UHFFFAOYSA-N chrysene Chemical compound C1=CC=CC2=CC=C3C4=CC=CC=C4C=CC3=C21 WDECIBYCCFPHNR-UHFFFAOYSA-N 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- XPPKVPWEQAFLFU-UHFFFAOYSA-J diphosphate(4-) Chemical compound [O-]P([O-])(=O)OP([O-])([O-])=O XPPKVPWEQAFLFU-UHFFFAOYSA-J 0.000 description 2
- 235000011180 diphosphates Nutrition 0.000 description 2
- 239000002360 explosive Substances 0.000 description 2
- 239000003906 humectant Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 230000001575 pathological effect Effects 0.000 description 2
- YNPNZTXNASCQKK-UHFFFAOYSA-N phenanthrene Chemical compound C1=CC=C2C3=CC=CC=C3C=CC2=C1 YNPNZTXNASCQKK-UHFFFAOYSA-N 0.000 description 2
- 125000005575 polycyclic aromatic hydrocarbon group Chemical group 0.000 description 2
- 229910000027 potassium carbonate Inorganic materials 0.000 description 2
- BBEAQIROQSPTKN-UHFFFAOYSA-N pyrene Chemical compound C1=CC=C2C=CC3=CC=CC4=CC=C1C2=C43 BBEAQIROQSPTKN-UHFFFAOYSA-N 0.000 description 2
- 238000000197 pyrolysis Methods 0.000 description 2
- 229940048084 pyrophosphate Drugs 0.000 description 2
- 239000002002 slurry Substances 0.000 description 2
- FQENQNTWSFEDLI-UHFFFAOYSA-J sodium diphosphate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OP([O-])([O-])=O FQENQNTWSFEDLI-UHFFFAOYSA-J 0.000 description 2
- 229940048086 sodium pyrophosphate Drugs 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 235000019818 tetrasodium diphosphate Nutrition 0.000 description 2
- 239000001577 tetrasodium phosphonato phosphate Substances 0.000 description 2
- DXBHBZVCASKNBY-UHFFFAOYSA-N 1,2-Benz(a)anthracene Chemical compound C1=CC=C2C3=CC4=CC=CC=C4C=C3C=CC2=C1 DXBHBZVCASKNBY-UHFFFAOYSA-N 0.000 description 1
- WKCZSFRAGKIIKN-UHFFFAOYSA-N 2-(4-tert-butylphenyl)ethanamine Chemical compound CC(C)(C)C1=CC=C(CCN)C=C1 WKCZSFRAGKIIKN-UHFFFAOYSA-N 0.000 description 1
- 241001156002 Anthonomus pomorum Species 0.000 description 1
- FMMWHPNWAFZXNH-UHFFFAOYSA-N Benz[a]pyrene Chemical compound C1=C2C3=CC=CC=C3C=C(C=C3)C2=C2C3=CC=CC2=C1 FMMWHPNWAFZXNH-UHFFFAOYSA-N 0.000 description 1
- XTEGARKTQYYJKE-UHFFFAOYSA-M Chlorate Chemical class [O-]Cl(=O)=O XTEGARKTQYYJKE-UHFFFAOYSA-M 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 239000004111 Potassium silicate Substances 0.000 description 1
- VSYMNDBTCKIDLT-UHFFFAOYSA-N [2-(carbamoyloxymethyl)-2-ethylbutyl] carbamate Chemical compound NC(=O)OCC(CC)(CC)COC(N)=O VSYMNDBTCKIDLT-UHFFFAOYSA-N 0.000 description 1
- 239000002250 absorbent Substances 0.000 description 1
- 230000002745 absorbent Effects 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 229910021538 borax Inorganic materials 0.000 description 1
- 229910052810 boron oxide Inorganic materials 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 235000019506 cigar Nutrition 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 230000001427 coherent effect Effects 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- LHRCREOYAASXPZ-UHFFFAOYSA-N dibenz[a,h]anthracene Chemical compound C1=CC=C2C(C=C3C=CC=4C(C3=C3)=CC=CC=4)=C3C=CC2=C1 LHRCREOYAASXPZ-UHFFFAOYSA-N 0.000 description 1
- UQGFMSUEHSUPRD-UHFFFAOYSA-N disodium;3,7-dioxido-2,4,6,8,9-pentaoxa-1,3,5,7-tetraborabicyclo[3.3.1]nonane Chemical compound [Na+].[Na+].O1B([O-])OB2OB([O-])OB1O2 UQGFMSUEHSUPRD-UHFFFAOYSA-N 0.000 description 1
- GVEPBJHOBDJJJI-UHFFFAOYSA-N fluoranthrene Natural products C1=CC(C2=CC=CC=C22)=C3C2=CC=CC3=C1 GVEPBJHOBDJJJI-UHFFFAOYSA-N 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- PMYUVOOOQDGQNW-UHFFFAOYSA-N hexasodium;trioxido(trioxidosilyloxy)silane Chemical compound [Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[O-][Si]([O-])([O-])O[Si]([O-])([O-])[O-] PMYUVOOOQDGQNW-UHFFFAOYSA-N 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000011147 inorganic material Substances 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- 150000002605 large molecules Chemical class 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- HZRMTWQRDMYLNW-UHFFFAOYSA-N lithium metaborate Chemical compound [Li+].[O-]B=O HZRMTWQRDMYLNW-UHFFFAOYSA-N 0.000 description 1
- PAZHGORSDKKUPI-UHFFFAOYSA-N lithium metasilicate Chemical compound [Li+].[Li+].[O-][Si]([O-])=O PAZHGORSDKKUPI-UHFFFAOYSA-N 0.000 description 1
- 229910052912 lithium silicate Inorganic materials 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 125000003367 polycyclic group Chemical group 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- OQZCJRJRGMMSGK-UHFFFAOYSA-M potassium metaphosphate Chemical compound [K+].[O-]P(=O)=O OQZCJRJRGMMSGK-UHFFFAOYSA-M 0.000 description 1
- 229940099402 potassium metaphosphate Drugs 0.000 description 1
- NNHHDJVEYQHLHG-UHFFFAOYSA-N potassium silicate Chemical compound [K+].[K+].[O-][Si]([O-])=O NNHHDJVEYQHLHG-UHFFFAOYSA-N 0.000 description 1
- 235000019353 potassium silicate Nutrition 0.000 description 1
- 229910052913 potassium silicate Inorganic materials 0.000 description 1
- JVUYWILPYBCNNG-UHFFFAOYSA-N potassium;oxido(oxo)borane Chemical compound [K+].[O-]B=O JVUYWILPYBCNNG-UHFFFAOYSA-N 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 230000001698 pyrogenic effect Effects 0.000 description 1
- PWZUUYSISTUNDW-VAFBSOEGSA-N quinestrol Chemical compound C([C@@H]1[C@@H](C2=CC=3)CC[C@]4([C@H]1CC[C@@]4(O)C#C)C)CC2=CC=3OC1CCCC1 PWZUUYSISTUNDW-VAFBSOEGSA-N 0.000 description 1
- 210000002345 respiratory system Anatomy 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000011684 sodium molybdate Substances 0.000 description 1
- 235000015393 sodium molybdate Nutrition 0.000 description 1
- TVXXNOYZHKPKGW-UHFFFAOYSA-N sodium molybdate (anhydrous) Chemical compound [Na+].[Na+].[O-][Mo]([O-])(=O)=O TVXXNOYZHKPKGW-UHFFFAOYSA-N 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- 239000004328 sodium tetraborate Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- TWQULNDIKKJZPH-UHFFFAOYSA-K trilithium;phosphate Chemical compound [Li+].[Li+].[Li+].[O-]P([O-])([O-])=O TWQULNDIKKJZPH-UHFFFAOYSA-K 0.000 description 1
- 239000003039 volatile agent 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
- A24B15/00—Chemical features or treatment of tobacco; Tobacco substitutes, e.g. in liquid form
- A24B15/18—Treatment of tobacco products or tobacco substitutes
- A24B15/24—Treatment of tobacco products or tobacco substitutes by extraction; Tobacco extracts
- A24B15/241—Extraction of specific substances
- A24B15/246—Polycyclic aromatic compounds
-
- A—HUMAN NECESSITIES
- A24—TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
- A24B—MANUFACTURE OR PREPARATION OF TOBACCO FOR SMOKING OR CHEWING; TOBACCO; SNUFF
- A24B15/00—Chemical features or treatment of tobacco; Tobacco substitutes, e.g. in liquid form
- A24B15/18—Treatment of tobacco products or tobacco substitutes
- A24B15/28—Treatment of tobacco products or tobacco substitutes by chemical substances
-
- A—HUMAN NECESSITIES
- A24—TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
- A24B—MANUFACTURE OR PREPARATION OF TOBACCO FOR SMOKING OR CHEWING; TOBACCO; SNUFF
- A24B15/00—Chemical features or treatment of tobacco; Tobacco substitutes, e.g. in liquid form
- A24B15/18—Treatment of tobacco products or tobacco substitutes
- A24B15/28—Treatment of tobacco products or tobacco substitutes by chemical substances
- A24B15/287—Treatment of tobacco products or tobacco substitutes by chemical substances by inorganic substances only
Definitions
- This invention relates to smoking compositions and to smokable articles including a novel class of inorganic material intimately associated with tobacco whereby the pyrogenesis of deleterious high-molecular weight substances normally encountered during the burning of tobacco particles is substantially reduced.
- known carcinogens contain at least four condensed benzene rings per molecule and may include derivatives and substitution products of benzanthracene, phenanthrene, pyrene, chrysene and other types of condensed-ring aromatic hydrocarbons.
- Certain of these highly carcinogenic compounds such as 1,2,5,6-dibenzanthracene and deriva tives of 3,4benzpyrene have been identified, whereas others are as yet unidentified or have not been resolved into individual molecular species.
- Such deleterious polycyclic hydrocarbons are undoubtedly of pyrogenic origin since they cannot be isolated from raw tobacco prior to the pyrolysis thereof.
- Such noxious substances are ordinarily carried as dispersed droplets or solid particles in the effluent smoke stream and thence into the smokers respiratory system along with the aroma and taste producing constituents of the smoke. Aside from their alleged pathological effect it appears that certain constituents of tars are in part responsible for a sharp, irritating taste imparted to smoke from a cigarette or the like.
- a tobacco composition including a novel treating solid which functions to substantially reduce the concentration in the smoke effluent from the mixture those deleterious high-molecular weight compounds, particularly polycyclic aromatic compounds, pyrogenetically or otherwise produced.
- Another object of the invention is the provision of a composition including tobacco intimately associated with a novel inorganic treating agent capable of lowering the burning temperature of the tobacco.
- the instant invention is the result of my discovery that the presence in smoking tobacco of certain inoxious incombustible solids capable of melting endothermically at a temperature at or below the burning temperature of the tobacco results in an improved smoking composition.
- innoxious refers not only to the quality of being noninjurious to health but also to the quality of being inoffensive to the senses.
- solids which melt endothermically at temperatures as low as about 300 C. may be used in the practice of the invention with some "benefit, nevertheless the melting of such a material will occur a distance from the advance of the flame-front and greater dissipation of the heat loss will occur than when the material employed undergoes endothermic melting at or within about C. of the flamefront temperature.
- the theoretically ideal material for the purposes of the instant invention is one which melts at the temperature of the flame-front for the particular tobacco-solid mix.
- materials melting endothermically from about 450 C. up to about the normal burning temperature of the particular tobacco in the absence of an added solid are particularly satisfactory for the purpose of my invention.
- Suitable solids for the purpose of my invention include innoxious solids melting endothermically without evolution of noxious volatiles and being non-explosive and nonoxidizing at the combustion temperature of the tobaccosolid mixture, the melting point of the pure solid being between about 4501000 C. and particularly from about 450 to 880 C. :30" C.
- Preferred solids are borates, phosphates, silicates, and hydrates thereof with cations selected from potassium, lithium, and sodium.
- Species include sodium tetraborate, soodium pyrophosphate, sodium disilicate, lithium metaborate, lithium silicate, lithium orthophosphate, potassium carbonate, potassium metaphosphate, and hydrates thereof.
- sodium molybdate, sodium pyrovanadate, boron oxide or hydrates thereof are also suitable.
- salts normally melting above the preferred range, suitable up to about 1000" C. may be used.
- potassium metaborate and potassium silicate, sodium pyrophosphate will generally be beneficially incorporated in the tobacco although they melt within the range of from about 880 1000" C.
- Nitrates and chlorates melting within the expressed temperature ranges are unsatisfactory because of their oxidizing nature and tendency to promote explosive combustion. Chlorides as well as sulfates are unsatisfactory because of possible evolution of noxious gases.
- the invention in its broadest aspect is not restricted to any specific quantity or range of quantities of salt additives.
- the optimum quantity is that which lowers the burning temperature of the tobacco mineral mixture to about 800 C. or more preferably to 720 C., or lower. In general from about 1 to 20%, and particularly from about 3 to 10%, based on the weight of tobacco, produces outstanding benefits.
- the specific amount of any particular meltable additive needed to reduce the burning temperature to a predetermined level will vary with the type of tobacco and the moisture content in the mixture. Other factors to be considered in determining the ratio of solid to tobacco include ability of the mixture to sustain burning, analysis of combustion product distribution, and taste and aroma of the eifluent smoke.
- the solid is preferably incorporated in the smoking unit in finely divided form, usually less than about microns and preferably having a substantial portion between about 0.5 and 2.0 microns. in general the more highly subdivided the solid the greater the adhesion to the tobacco. It has been found that coarser particles, for example 44 micron particles, are more prone than more finely-divided particles to pass into the smokers mouth.
- coarser particles for example 44 micron particles
- the particular range of particle size used in a tobaccosolid mix will depend on such factors as moisture content, presence of tacky humectants, presence of an agent to bind the mineral to the tobacco surface, mode of application to the tobacco, size of tobacco particles, presence of and nature of filter-tip in the smoking unit, quantity of solid used and locus of solid placement.
- a filter is preferably employed in a smoking unit when tobacco is treated by the process herein taught.
- the filter may be fibrous and/ or include absorbents such as silica, clay or the like.
- the purpose of the filter is to prevent any inspiration of finely-divided particles which may occur if the smoking unit is subjected to dry warm weather for prolonged periods.
- the filter imposes a bed of material capable of entraining the particle which might otherwise be drawn into the smokers mouth.
- the filter may be omitted.
- Example I A cigarette of the present invention is prepared by admixing 1.0 gram of pre-humected cigarette tobacco (a blend adapted to burn at a peak temperature of about 880 C.) with 0.05 gram of pulverized sodium metaphosphate and packing the tobacco mix into a cylindrical cigarette-paper having a fibrous filter-tip.
- Example 11 0.04 gram of the potassium pentaborate is intermingled with 1.0 gram of cigarette tobacco and the mixture is made into a cigarette as in Example I.
- Example III A dilute aqueous solution of sodium metaborate is sprayed on shredded blended tobacco in amount sufficient to leave a residue of 0.05 gram of the salt (calculated as NaBO resident on each 1.0 gram of tobacco (moisturefree basis).
- the invention is not restricted to any method of commingling the tobacco and solid, any suitable means for intimately associating the components being satisfactory.
- a slurry of salt particles may be added to leaf or particulated tobacco, suitably by spraying a slurry of the mineral particles onto the tobacco.
- Water-soluble salts may be dissolved prior to spraying onto the tobacco.
- a salt, watersoluble or water-insoluble can be incorporated into socalled homogenized leaf tobacco by forming comrninuted tobacco and salt into a coherent sheet-like mass with the aid of a suitable binder.
- a smoking mixture consisting essentially of tobacco shreds having mixed therewith from 3% to 10% by weight of finely-divided solid particles of an alkali metal salt of an acid selected from the group consisting of silicates, phosphates and borates, and which has a melting point within the range of 450 C. to 1000 C., said tobacco shreds consisting essentially of naturally occurring tobacco.
- a smoking mixture comprising essentially tobacco shreds having uniformly mixed therewith from 3% to 10% by weight of finely-divided solid particles of sodium metaphosphate as the sole phosphate additive.
- a smoking mixture comprising essentially tobacco shreds having uniformly mixed therewith from 3% to 10% by weight of finely-divided solid particles of potassium pentaborate.
- a smoking mixture comprising essentially tobacco shreds having uniformly mixed therewith from 3% to 10% by Weight of finely-divided solid particles of sodium metaborate.
- a cigarette consisting essentially of shreds of tobacco having incolporated therewith from 3% to 10% by weight of finely-divided solid particles of an alkali-metal salt of an acid selected from the group consisting of silicates, phosphates and borates and which has a melting point within the range of 450 C. to 1000 C., said tobacco shreds consisting essentially of naturally occurring tobacco.
- a smoking tobacco mixture comprising tobacco and about 1 percent to about 10 percent by weight of the tobacco of boric oxide, said boric oxide serving to lower the maximum burning temperature of the tobacco.
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Toxicology (AREA)
- Inorganic Chemistry (AREA)
- Manufacture Of Tobacco Products (AREA)
Description
United States Patent Walter Linwood Haden, .lru, Metuchen, NJ, assignor to Minerals & Chemicals Philipp Corporation, a corporation of Maryland No Drawing. Filed Nov. 14, 1957, Ser. No. 696,314
9 Claims. (Cl. 13117) This invention relates to smoking compositions and to smokable articles including a novel class of inorganic material intimately associated with tobacco whereby the pyrogenesis of deleterious high-molecular weight substances normally encountered during the burning of tobacco particles is substantially reduced.
There exists strong clinical, statistical and pathological evidence that certain constituents of tobacco smoke condensate are potentially carcinogenic when deposited on human tissue. These carcinogens have been reported to be mixtures of essentially neutral high-molecular weight polycyclic aromatic hydrocarbons, the carcinogenic potency of any mixture depending on the species present. Several general types of polycyclic aromatic hydrocarbons are present in a carcinogenic fraction of such smoke condensate, or tar, and undoubtedly many individual molecular species are hence present. In general, known carcinogens contain at least four condensed benzene rings per molecule and may include derivatives and substitution products of benzanthracene, phenanthrene, pyrene, chrysene and other types of condensed-ring aromatic hydrocarbons. Certain of these highly carcinogenic compounds such as 1,2,5,6-dibenzanthracene and deriva tives of 3,4benzpyrene have been identified, whereas others are as yet unidentified or have not been resolved into individual molecular species. Such deleterious polycyclic hydrocarbons are undoubtedly of pyrogenic origin since they cannot be isolated from raw tobacco prior to the pyrolysis thereof.
Such noxious substances are ordinarily carried as dispersed droplets or solid particles in the effluent smoke stream and thence into the smokers respiratory system along with the aroma and taste producing constituents of the smoke. Aside from their alleged pathological effect it appears that certain constituents of tars are in part responsible for a sharp, irritating taste imparted to smoke from a cigarette or the like.
There is strong indication that the generation of these allegedly carcinogenic compounds is favored by high temperatures, whereby they are present in greater quantity in the tars from a cigarette than in the tars from a cigar or pipe, which when smoked develop peak temperatures several hundred degrees lower than that of a cigarette. At the peak temperature of about 880 C. :35 C. developed in a conventional cigarette when puffed such carcinogens are generated in potentially dangerous quantities. There is good evidence that the lowering of this peak to 800 C. or less results in decreased generation of the potentially carcinogenic substances with substantial benefits accruing from lowering the burning temperature to about 720 C. or less.
Accordingly, it is a principal object of the instant invention to provide a tobacco composition including a novel treating solid which functions to substantially reduce the concentration in the smoke effluent from the mixture those deleterious high-molecular weight compounds, particularly polycyclic aromatic compounds, pyrogenetically or otherwise produced.
It is another object of the invention to incorporate a novel treating solid in smoking tobacco to permit the pyrolysis of said tobacco to take place to a lower tem- 3,126,011 Patented Mar. 24, 1964 I perature than would be encountered in the absence of said treating solid.
Another object of the invention is the provision of a composition including tobacco intimately associated with a novel inorganic treating agent capable of lowering the burning temperature of the tobacco.
It is another object of the invention to provide smoking units including such compositions which inherently possess the ability to simultaneously improve the aroma of the smoke from the tobacco and substantially prevent the generation of deleterious high-molecular weight polycyclic compounds.
Other objects will be apparent from an inspection of the following description of the invention.
The instant invention is the result of my discovery that the presence in smoking tobacco of certain inoxious incombustible solids capable of melting endothermically at a temperature at or below the burning temperature of the tobacco results in an improved smoking composition. The term innoxious as used herein refers not only to the quality of being noninjurious to health but also to the quality of being inoffensive to the senses. Although solids which melt endothermically at temperatures as low as about 300 C. may be used in the practice of the invention with some "benefit, nevertheless the melting of such a material will occur a distance from the advance of the flame-front and greater dissipation of the heat loss will occur than when the material employed undergoes endothermic melting at or within about C. of the flamefront temperature. The theoretically ideal material for the purposes of the instant invention is one which melts at the temperature of the flame-front for the particular tobacco-solid mix. In general, materials melting endothermically from about 450 C. up to about the normal burning temperature of the particular tobacco in the absence of an added solid are particularly satisfactory for the purpose of my invention.
Suitable solids for the purpose of my invention include innoxious solids melting endothermically without evolution of noxious volatiles and being non-explosive and nonoxidizing at the combustion temperature of the tobaccosolid mixture, the melting point of the pure solid being between about 4501000 C. and particularly from about 450 to 880 C. :30" C. Preferred solids are borates, phosphates, silicates, and hydrates thereof with cations selected from potassium, lithium, and sodium. Species include sodium tetraborate, soodium pyrophosphate, sodium disilicate, lithium metaborate, lithium silicate, lithium orthophosphate, potassium carbonate, potassium metaphosphate, and hydrates thereof. Also suitable are sodium molybdate, sodium pyrovanadate, boron oxide or hydrates thereof. When the composition of the ash constituents originating in the tobacco or treating agents is such that additives normally melting above 880 :30 C. form lower melting mixtures, salts normally melting above the preferred range, suitable up to about 1000" C. may be used. For this reason potassium metaborate and potassium silicate, sodium pyrophosphate, will generally be beneficially incorporated in the tobacco although they melt within the range of from about 880 1000" C.
Nitrates and chlorates melting within the expressed temperature ranges are unsatisfactory because of their oxidizing nature and tendency to promote explosive combustion. Chlorides as well as sulfates are unsatisfactory because of possible evolution of noxious gases.
It will be understood that the invention in its broadest aspect is not restricted to any specific quantity or range of quantities of salt additives. The optimum quantity is that which lowers the burning temperature of the tobacco mineral mixture to about 800 C. or more preferably to 720 C., or lower. In general from about 1 to 20%, and particularly from about 3 to 10%, based on the weight of tobacco, produces outstanding benefits. The specific amount of any particular meltable additive needed to reduce the burning temperature to a predetermined level will vary with the type of tobacco and the moisture content in the mixture. Other factors to be considered in determining the ratio of solid to tobacco include ability of the mixture to sustain burning, analysis of combustion product distribution, and taste and aroma of the eifluent smoke.
The solid is preferably incorporated in the smoking unit in finely divided form, usually less than about microns and preferably having a substantial portion between about 0.5 and 2.0 microns. in general the more highly subdivided the solid the greater the adhesion to the tobacco. It has been found that coarser particles, for example 44 micron particles, are more prone than more finely-divided particles to pass into the smokers mouth. Of course the particular range of particle size used in a tobaccosolid mix will depend on such factors as moisture content, presence of tacky humectants, presence of an agent to bind the mineral to the tobacco surface, mode of application to the tobacco, size of tobacco particles, presence of and nature of filter-tip in the smoking unit, quantity of solid used and locus of solid placement.
A filter, either of the well-known type which is integral with the smoking unit or of the holder type including a filter, is preferably employed in a smoking unit when tobacco is treated by the process herein taught. The filter may be fibrous and/ or include absorbents such as silica, clay or the like. The purpose of the filter is to prevent any inspiration of finely-divided particles which may occur if the smoking unit is subjected to dry warm weather for prolonged periods. The filter imposes a bed of material capable of entraining the particle which might otherwise be drawn into the smokers mouth. However, by proper selection of moisture content and, in some cases, inclusion of about 2 to 4% (based on the weight of the tobacco) of humectant or by otherwise bonding the minerals to the tobacco surface the filter may be omitted.
Although the description of the invention has been made with particular reference to cigarettes, it will be understood that the practice as herein taught is applicable to any smoking unit.
The following examples are given only for the sake of further illustrating the invention and are not to be construed as limiting the scope thereof.
Example I A cigarette of the present invention is prepared by admixing 1.0 gram of pre-humected cigarette tobacco (a blend adapted to burn at a peak temperature of about 880 C.) with 0.05 gram of pulverized sodium metaphosphate and packing the tobacco mix into a cylindrical cigarette-paper having a fibrous filter-tip.
Example 11 0.04 gram of the potassium pentaborate is intermingled with 1.0 gram of cigarette tobacco and the mixture is made into a cigarette as in Example I.
Example III A dilute aqueous solution of sodium metaborate is sprayed on shredded blended tobacco in amount sufficient to leave a residue of 0.05 gram of the salt (calculated as NaBO resident on each 1.0 gram of tobacco (moisturefree basis).
Furthermore, the invention is not restricted to any method of commingling the tobacco and solid, any suitable means for intimately associating the components being satisfactory. For example, when the salt is water-insoluble or substantially water-insoluble a slurry of salt particles may be added to leaf or particulated tobacco, suitably by spraying a slurry of the mineral particles onto the tobacco. Water-soluble salts may be dissolved prior to spraying onto the tobacco. Likewise, a salt, watersoluble or water-insoluble, can be incorporated into socalled homogenized leaf tobacco by forming comrninuted tobacco and salt into a coherent sheet-like mass with the aid of a suitable binder.
Obviously, many modifications and variations of the invention as hereinbefore set forth may be made without departing from the spirit and scope thereof, and therefore, only such limitations should be imposed as are indicated in the appended claims.
I claim:
1. A smoking mixture consisting essentially of tobacco shreds having mixed therewith from 3% to 10% by weight of finely-divided solid particles of an alkali metal salt of an acid selected from the group consisting of silicates, phosphates and borates, and which has a melting point within the range of 450 C. to 1000 C., said tobacco shreds consisting essentially of naturally occurring tobacco.
2. A smoking mixture comprising essentially tobacco shreds having uniformly mixed therewith from 3% to 10% by weight of finely-divided solid particles of sodium metaphosphate as the sole phosphate additive.
3. A smoking mixture comprising essentially tobacco shreds having uniformly mixed therewith from 3% to 10% by weight of finely-divided solid particles of potassium pentaborate.
4. A smoking mixture comprising essentially tobacco shreds having uniformly mixed therewith from 3% to 10% by Weight of finely-divided solid particles of sodium metaborate.
5. A cigarette consisting essentially of shreds of tobacco having incolporated therewith from 3% to 10% by weight of finely-divided solid particles of an alkali-metal salt of an acid selected from the group consisting of silicates, phosphates and borates and which has a melting point within the range of 450 C. to 1000 C., said tobacco shreds consisting essentially of naturally occurring tobacco.
6. The cigarette of claim 5 in which said salt is sodium metaphosphate.
7. The cigarette of claim 5 in which said salt is potassium pentaborate.
8. The cigarette of claim 5 in which said salt is sodium metaborate.
9. A smoking tobacco mixture comprising tobacco and about 1 percent to about 10 percent by weight of the tobacco of boric oxide, said boric oxide serving to lower the maximum burning temperature of the tobacco.
References Cited in the file of this patent UNITED STATES PATENTS 467,055 Schneider Jan. 12, 1892 604,338 Rickard et a1 May 17, 1898 1,996,002 Seaman Mar. 26, 1935 2,029,494 Loewenthal Feb. 4, 1936 2,108,860 Kaufi'man Feb. 22, 1938 2,329,927 Morton Sept. 21, 1943 2,613,673 Sartoretto et al. Oct. 14, 1952 2,776,916 Ericcson Jan. 8, 1957 2,786,471 Graybeal Mar. 26, 1957 2,808,057 Jaksch Oct. 1, 1957 2,839,065 Milton June 17, 1958 2,914,072 Tyrer Nov. 24, 1959 FOREIGN PATENTS 671,126 Germany Jan. 31, 1939 869,465 Germany Nov. 12, 1953 OTHER REFERENCES Making Cigarettes Safe, from Time, Apr. 22, 1957 (p UNITED STATES PATENT OFFICE CERTIFICATE OF CORRECTION Patent No. 3,126,011 March 24, 1964 Walter Linwood Haden, Jr.
It is hereby certified that error appears in the above numbered patent requiring correction and that the said Letters Patent should read as corrected below.
Column 2, line 47, for "soodium pyrophosphate" read sodium pyrophosphate line 49, for "potassium carbonate" read potassium pentaborate column 2, line 54,
for "above 8803 30 C, read above 880-1530 Co Signed and sealed this 14th day of July 1964,
(SEAL) Attest:
ESTON G. JOHNSON EDWARD J. BRENNER Attesting Officer Commissioner of Patents
Claims (1)
1. A SMOKING MIXTURE CONSISTING ESSENTIALLY OF TOBACCO SHREDS HAING MIXED THEREWITH FROM 3% TO 10% BY WEIGHT OF FINELY-DIVIDED SOLID PARTICLES OF AN ALKALI METAL SALT OF AN ACID SELECTED FROM THE GROUP CONSISTING OF SILICATES, PHOSPHATES AND BORATES, AND WHICH HAS A MELTING POINT WITHIN THE RANGE OF 450*C. TO 1000*C., SAID TOBACCO SHREDS CONSISTING ESSENTIALLY OF NATURALLY OCCURRING TOBACO.
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3126011A true US3126011A (en) | 1964-03-24 |
Family
ID=3455179
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US3126011D Expired - Lifetime US3126011A (en) | Tobacco composition and smoking unit |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US3126011A (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3474792A (en) * | 1966-08-05 | 1969-10-28 | Eastman Kodak Co | Treatment of smoking tobacco with chlorate salts |
| US3577997A (en) * | 1969-03-20 | 1971-05-11 | American Chemosol Corp | Tobacco treatment with citric acid and deuterium oxide |
| EP0034922B1 (en) * | 1980-02-21 | 1985-05-22 | Philip Morris Incorporated | Tobacco treatment |
| US20040112394A1 (en) * | 2002-07-18 | 2004-06-17 | Val Krukonis | Reduction of constituents in tobacco |
| EP1432322A4 (en) * | 2001-08-31 | 2010-08-18 | Philip Morris Prod | Tobacco smoking mixture for smoking articles such as cigarettes |
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| US467055A (en) * | 1892-01-12 | Cured tobacco | ||
| US604338A (en) * | 1898-05-17 | Art of treating tobacco-leaves | ||
| US1996002A (en) * | 1933-05-25 | 1935-03-26 | Seaman Stewart Elmer | Decreasing inflammability of cigarettes |
| US2029494A (en) * | 1933-02-13 | 1936-02-04 | Fed Tobacco Corp | Treatment of tobacco |
| US2108860A (en) * | 1934-11-12 | 1938-02-22 | Paul Bechtner | Method of and substance for treating tobacco smoke |
| DE671126C (en) * | 1936-04-01 | 1939-01-31 | Leopold Oppenheimer Dipl Ing | Process for bleaching tobacco |
| US2329927A (en) * | 1938-04-28 | 1943-09-21 | Joseph B Morton | Method of and composition for treating cigarettes, cigarette paper, and tobacco |
| US2613673A (en) * | 1946-07-11 | 1952-10-14 | Int Cigar Mach Co | Tobacco sheet material and method of producing the same |
| DE869465C (en) * | 1950-10-31 | 1953-11-12 | Kurt Koerber & Co K G | Procedure for deleting the cigarette residue |
| US2776916A (en) * | 1954-08-23 | 1957-01-08 | Ralph L Ericsson | Tobacco composition |
| US2786471A (en) * | 1953-04-13 | 1957-03-26 | Graybeal Kenneth Wayne | Cigarettes |
| US2808057A (en) * | 1955-03-11 | 1957-10-01 | Matthias F Jaksch | Cigarette and filter therefor |
| US2839065A (en) * | 1956-05-21 | 1958-06-17 | Union Carbide Corp | Filter for tobacco smoke |
| US2914072A (en) * | 1955-01-31 | 1959-11-24 | Tyrer Daniel | Process of improving the smoking qualities of tobacco |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US467055A (en) * | 1892-01-12 | Cured tobacco | ||
| US604338A (en) * | 1898-05-17 | Art of treating tobacco-leaves | ||
| US2029494A (en) * | 1933-02-13 | 1936-02-04 | Fed Tobacco Corp | Treatment of tobacco |
| US1996002A (en) * | 1933-05-25 | 1935-03-26 | Seaman Stewart Elmer | Decreasing inflammability of cigarettes |
| US2108860A (en) * | 1934-11-12 | 1938-02-22 | Paul Bechtner | Method of and substance for treating tobacco smoke |
| DE671126C (en) * | 1936-04-01 | 1939-01-31 | Leopold Oppenheimer Dipl Ing | Process for bleaching tobacco |
| US2329927A (en) * | 1938-04-28 | 1943-09-21 | Joseph B Morton | Method of and composition for treating cigarettes, cigarette paper, and tobacco |
| US2613673A (en) * | 1946-07-11 | 1952-10-14 | Int Cigar Mach Co | Tobacco sheet material and method of producing the same |
| DE869465C (en) * | 1950-10-31 | 1953-11-12 | Kurt Koerber & Co K G | Procedure for deleting the cigarette residue |
| US2786471A (en) * | 1953-04-13 | 1957-03-26 | Graybeal Kenneth Wayne | Cigarettes |
| US2776916A (en) * | 1954-08-23 | 1957-01-08 | Ralph L Ericsson | Tobacco composition |
| US2914072A (en) * | 1955-01-31 | 1959-11-24 | Tyrer Daniel | Process of improving the smoking qualities of tobacco |
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Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3474792A (en) * | 1966-08-05 | 1969-10-28 | Eastman Kodak Co | Treatment of smoking tobacco with chlorate salts |
| US3577997A (en) * | 1969-03-20 | 1971-05-11 | American Chemosol Corp | Tobacco treatment with citric acid and deuterium oxide |
| EP0034922B1 (en) * | 1980-02-21 | 1985-05-22 | Philip Morris Incorporated | Tobacco treatment |
| US4589428A (en) * | 1980-02-21 | 1986-05-20 | Philip Morris Incorporated | Tobacco treatment |
| EP1432322A4 (en) * | 2001-08-31 | 2010-08-18 | Philip Morris Prod | Tobacco smoking mixture for smoking articles such as cigarettes |
| US20040112394A1 (en) * | 2002-07-18 | 2004-06-17 | Val Krukonis | Reduction of constituents in tobacco |
| US7798151B2 (en) * | 2002-07-18 | 2010-09-21 | Us Smokeless Tobacco Co. | Reduction of constituents in tobacco |
| US20110067715A1 (en) * | 2002-07-18 | 2011-03-24 | Us Smokeless Tobacco Co. | Reduction of constituents in tobacco |
| US8555895B2 (en) | 2002-07-18 | 2013-10-15 | U.S. Smokeless Tobacco Company Llc | Reduction of constituents in tobacco |
| US10045557B2 (en) | 2002-07-18 | 2018-08-14 | Us Smokeless Tobacco Co. | Reduction of constituents in tobacco |
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