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US2809637A - Improved tobacco products and cigarette paper and methods of making same - Google Patents

Improved tobacco products and cigarette paper and methods of making same Download PDF

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Publication number
US2809637A
US2809637A US196339A US19633950A US2809637A US 2809637 A US2809637 A US 2809637A US 196339 A US196339 A US 196339A US 19633950 A US19633950 A US 19633950A US 2809637 A US2809637 A US 2809637A
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Prior art keywords
complex
chlorophyll
chloroplastic
paper
cigarette paper
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US196339A
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William J Hale
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Verdurin Co
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Verdurin Co
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    • AHUMAN NECESSITIES
    • A24TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
    • A24BMANUFACTURE OR PREPARATION OF TOBACCO FOR SMOKING OR CHEWING; TOBACCO; SNUFF
    • A24B15/00Chemical features or treatment of tobacco; Tobacco substitutes, e.g. in liquid form
    • A24B15/18Treatment of tobacco products or tobacco substitutes
    • A24B15/28Treatment of tobacco products or tobacco substitutes by chemical substances
    • A24B15/30Treatment of tobacco products or tobacco substitutes by chemical substances by organic substances
    • A24B15/302Treatment of tobacco products or tobacco substitutes by chemical substances by organic substances by natural substances obtained from animals or plants
    • A24B15/303Plant extracts other than tobacco
    • AHUMAN NECESSITIES
    • A24TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
    • A24BMANUFACTURE OR PREPARATION OF TOBACCO FOR SMOKING OR CHEWING; TOBACCO; SNUFF
    • A24B15/00Chemical features or treatment of tobacco; Tobacco substitutes, e.g. in liquid form
    • A24B15/18Treatment of tobacco products or tobacco substitutes
    • A24B15/28Treatment of tobacco products or tobacco substitutes by chemical substances
    • A24B15/281Treatment of tobacco products or tobacco substitutes by chemical substances the action of the chemical substances being delayed
    • A24B15/282Treatment of tobacco products or tobacco substitutes by chemical substances the action of the chemical substances being delayed by indirect addition of the chemical substances, e.g. in the wrapper, in the case
    • AHUMAN NECESSITIES
    • A24TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
    • A24BMANUFACTURE OR PREPARATION OF TOBACCO FOR SMOKING OR CHEWING; TOBACCO; SNUFF
    • A24B15/00Chemical features or treatment of tobacco; Tobacco substitutes, e.g. in liquid form
    • A24B15/18Treatment of tobacco products or tobacco substitutes
    • A24B15/28Treatment of tobacco products or tobacco substitutes by chemical substances
    • A24B15/42Treatment of tobacco products or tobacco substitutes by chemical substances by organic and inorganic substances

Definitions

  • chloroplastic complex embraces generally the total composition of plant chloroplast exclusive of the cellulosic components and includes Waxes, sterols and phospholipids.
  • the phospholipids play no chemical role in the present invention but present or exert no deleterious effect.
  • chloroplastic complex is to be understood as dcfining the entire unresolved catalyst and pigment within the stroma of chloroplasts of living plant cells.

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  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Toxicology (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Agronomy & Crop Science (AREA)
  • Botany (AREA)
  • Manufacture Of Tobacco Products (AREA)

Description

E/HROVED TOBACCO PRODUCTS AND CIGA- ISRETTE PAPER AND METHODS OF MAKING J. Hale, Midland, Mich, assignor to Verdnrin Company, Detroit, Mich, a corporation of Michigan No Drawing. Application November 17, 1950, Serial No. 196,339
8 Claims. (Cl. 131-9) This invention relates to methods of treating tobacco and improved tobacco compositions and appurtenances. In my earlier patent U. S. 2,460,284 issued February 1, 1949 it was shown that when cured tobacco receives an additional treatment with solubilized chlorophyll, or it related compounds, the finished tobacco, in the process of smoking, undergoes a fuller oxidation by reason of a continuous supply of activated oxygen evolved directly from the chlorophyll distributed throughout the tobacco. In like manner my patent U. S. 2,460,285 issued February 1, 1949 discloses the fuller oxidation or" cigarette paper when said paper carries a small portion of solubilized chlorophyll distributed therethrough. To the accomplishment of ends above cited it was found most practical to spray tobacco, as well as its wrapper, with an alcoholic solution of chlorophyll, or with an aqueous solution of Water-soluble chlorophyll, such as chlorophyllins, and allow the material to dry.
The procedure here described leads to a highly extended surface of chlorophyll, preferably in that of-its most active formwater-solution chlorophyllin. In the presence of air, however, there is ever a tendency of the chlorophyllin to undergo decomposition by way of autoxidation, especially in summer weather. Hence it has become necessary to seek some means of protecting chlorophyllin if there is to be any assurance of its readiness at all times to function as an oxidant.
In nature herself we have the answer. Here we find not alone a protectant to the porphyrin, chlorophyll, but also a protectant to this protectant. The first protectant, as well known, is made up of carotenoids, notably alpha, beta and gamma carotenes, which function both in speeding up the oxidizing action of chlorophyll and in repressing excessive oxygen from destroying chlorophyll. The second protectant is alpha tocopherol (vitamin E) which protects both chlorophyll and especially the carotenoids against their own oxidation. There are still other protectants, among the concomitants of chlorophyll in nature, not the least of which is vitamin K, especially protective against oxidation of unsaturated molecules even when it is present in less than one-millionth part. Both vitamin E and vitamin K are known structurally as quinoids.
Commercial chlorophyll is extracted directly from dried green leaves, chiefly alfalfa. Degradation of verdure through the action of an association of solvents leads to complete break-down of the chloroplasts that constitute the seat of oxidative-reductive activity resident in a living plant. In this break-down chlorophyll, its congeners and concomitants together with enzyme aggregates, are totally resolved into the individual components and separated chromatographically. Heretofore, no practical application of the entire oxidativereductive unit existant in the stroma of chloroplast has been possible, simply for the reason that up to within a few years this truly physiological unit had not been 1 isolatable as such.
ice
Fortunately, of late, the Berkman chlorophyll-unit as described in U. S. Patent 2,567,362 issued Sept. 11, 1951; has come into the market. This unit is composed of chlorophyll-a; chlorophyll-b; alpha, beta and gamma carotenes; lycopene; xanthophyll; alpha tocopherol (vitamin E); methyl phytyl naphthoquinone (vitamin K) and certain lipids, the last named serving chiefly as protective coating. The whole of this unit may be described as the physiological unit of plant life, and a complex pigment nuclei embedded in a phospholipid. In this context thi physiological unit will be described as chlorophyll-carotenoid-quinoid complex. This complex embraces generally the total composition of plant chloroplast exclusive of the cellulosic components and includes Waxes, sterols and phospholipids. The phospholipids play no chemical role in the present invention but present or exert no deleterious effect. Hence more explicitly the term chloroplastic complex is to be understood as dcfining the entire unresolved catalyst and pigment within the stroma of chloroplasts of living plant cells.
Resolution of the chloroplastic complex into respective green chlorophyll and orange carotenoid fractions may readily be effected, but the original aggregate is most outstanding to all purposes. Primarily is this chloroplastic complex noted for its stability to light and heat and for its oxidative activity operative without danger to its own self-oxidation.
Closeness of composition between this physiological unit or chloroplastic complex, as now securable in the market, and the actual unit or complex as existant within the green leaf has been well demonstrated through chemical analysis; and studies carried out to compare the oxidizing effect of said chloroplastic complex over against that of just plain chlorophyll of commerce gave most interesting results as is illustrated by the following experiments.
Experiment 1 Into a three-necked flask, carrying 1 gram of sodiun copper chlorophyllin dissolved in 1000 cc. of distilled water at 30 C., and properly fitted with inlet and outlet tubes and thermometer, was passed a current of 10,000 cc. of carbon monoxide and 25,000 cc. of air at same temperature, and in the course of one hour. The resulting car bon dioxide, collected in lime water amounted to 2.10 grams (complete oxidation of 10 liters of carbon monoxide would have yielded 19.80 grams of the CO2).
Experiment 2 Into the same flask, as in Experiment 1, there was admitted 1 gram of the physiological chlorophyll unit suspended in 1000 cc. of distilled water, at 30 C. and a current of 10,000 cc. of carbon monoxide and 25,000 cc. of air at the same temperature, passed through the flask in the course of one hour. The carbon dioxide collected from effluent gas weighed 4.56 grams. Complete oxidation of these 12.50 grams (10,000 cc.) of carbon monoxide would have yielded 19.8 grams of CO2.
Hence the oxidation of carbon monoxide by chloro phyll, though siow enough at 30 C. is actually doubled (or is twice as eitective) under the influence of the physiological chlorophyll unit. Difficult as it is in dealing with an insoluble agent the marked efiectiveness here of the chloroplastic complex is clearly demonstrated. So great is the effectiveness of this chloroplastie complex, and other analogous porphyrin-carotenoid-quinoid complexes, that even when adsorbed chromatographically upon an adsorbent, it can be shown that its efiect upon passing vapors is in no way repressed. Rather, it is increased. Certain toxic vapors such as carbon monoxide and aldehydic vapors from burning tobacco were proved to be greatly reduced by an adsorbed chloroplasti-c 7 'weight of total cigarette.
afforded this chloroplastic complex by the refractory nature of adsorbent itself. Thus, there is established a novel a procedure for contacting, for example, tobacco and its wrappers with an oxidative catalyst, not highly diminuted and dispersed through the actually combustible cellulosic or other organic media, but one that is encased within a shield resistant to confiagration up to the point where interior of shield reaches the temperature of decomposition of catalyst.
It is here that cigarette paper ofiers an ideal locale for experimental observation. Some 20-45% of the weight of cigarette paper is made up of. calcium carbonate to promote slow and even burning of paper and likewise to present a'highly desirable whiteness to the paper itself. The weight of cigarette paper is approximately of the In the earlier patent, above cited, the cigarette paper as such inthe early pulp stage was sprayed with chlorophyll solution and the green-colc-red pulp finished by impregnation with calcium-carbonate. The result is, of course, a green-colored cigarette paper. By employing this new procedure it is possible to introduce ordinary chlorophyll into the calcium carbonate or filler and in turn tointroduce this filler into cigarette at time of finishing'said paper. The result is still a greencolored cigarette, little more to be preferred over the procedure' outlined in the earlier patent. V
Whenthe physiological chlorophyll unit, i. e.,'the chloroplastic complex, or a chemically similar unit of porphyrin-carotenoid-quinoid type, is made to enter this pic- V ture, an entirely new panorama is presented. This insoluble chloroplastic complex cannot be applied as a spray. It can, however, be triturated with calcium carbonate; and as an adsorbent this calcium carbonate (as 7 well also as other earth metal bases) withdraws to itself more deeply the green chlorophyll and next following the orange carotenoids, with the result that the triturate of calcium carbonate with chloroplastic complex is of the faintest yellow if there is only so .much as 20 times as much base as organic complex. I'n'the finished cigarette paper the concentration of the chloroplastic complex in the weight of calcium carbonate used will scarcely exceed 1 part in 200. Hence the color of finished cigarette paper will differ only slightly (on the yellowish gray side) from the generally accepted white paper.
This invention, therefore, comprehends the employment of chlorophyll-carotenoid-quinoid lipidized calcium carbonate, or other White insoluble oxides or carbonates herein suited, intermingled withcigarette paper at the end of the pulp stage in manufacture. The percentage of chloroplastic complex in total weight of paper, on dry basis, may varybetween the. limits of approximately of 1% to not in excess of 2% for the attainment of ends heredesired, namely, a fuller oxidation of the more volatile aldehydic vapors as Well also as oxidation of greater portion of carbon monoxide issuing from the cigarette both in primary smoke (entering the mouth) and in secondary smoke (escapingdirectly from the lighted cigarette). 1 a
This invention comprehends further the employment of cigarette paper so impregnated with chlorophyll-carotenoid-quinoid-lipidized calcium carbonate in the wrap ping for, shredded tobacco likewise impregnated with similar percentage of chlorophyll-carotenoid-quinoid-lipidized calcium carbonate or with. the usual form of shredded tobacco not so impregnated.
The marketable advantage of this invention resides in the blanking out of the somewhat undesirable green tinge in color of cigarette paper that has been treated with generally procurable water-soluble chlorophyll or even with solubilized chlorophyll as cited in my above mentioned patents.
The practical advantage-of this invention resides in the graded diffusion 'of various components of the chloroplastic complex within the calcium carbonate particles such that the green or chlorophyllic portion becomes more deeply adsorbed whereas the orange or carotenoid portion left on the surface of said particles constitutes the more heat-resistantportion and servesto protect longer the interior portion, yetboth at all times functioning together syngertistically as oxidants for toxic vapors that pass near or over the particles.
The cahracterizing feature ofth'is' invention resides in the depositing of an insoluble active oxidant within the interstices of an inorganic refractory adsorbent thereby to increase protection of the entire oxidant against light and heat, as contrasted with same oxidant contained within the interstices ofan easily charrable and decomposable organic medium as is tobacco and its wrapper, and as set forth in my. above mentioned patents The' composite oxidant here is far more effective than ordinary chlorophyll be it highly dispersed throughout the organic medium or actually carriedin the filler. At all events this invention presents a means of materially prolonging the i oxidizing action of chlorophyll.
" generally, does not exceed 20 to 25% of the weight of i pulp and filler well intermingled; hereby, the total weight triturate once it is prepared.
The method of procedure in carrying out this invention comprehendssimply a trituration of desired quantity of chloroplastic complex with the given quantity of precipitated calcium carbonate, or similar white base; the latter dry cigarette paper pulp. On the basis of grams'of cigarette paper pulp (dry basis), 25 grams of precipitated calcium carbonate will be triturated thronghly with 0.1 gram of chloroplastic complex (in fine powder), and the of finished paper will carry of 1% oxidant.
Another method of applying the triturate of precipitated chalk and chloroplastic complex comprises dusting the cigarette paper with the triturate just prior to passing the paper through the final finishing rolls. However, the distribution or. interspersion of the triturateis not as well assured by this procedure.
In'the case of shredded tobacco a much smaller proportion of' calcium carbonate is called for; hence approximately this same precentage of chloroplastic complex will need-be triturated with only a few grams oflcalcium carbonate and the triturate throroughly rubbed into the tobacco. a
Another practical procedure, somewhat saving in cost,
contributory to involvement of the maximum number of calcium carbonate particles, consists in triturating green leaves directly with calcium carbonate or other white inert adsorbent. If the leaves have lost too much of their water content a trace of water or other solvent may be added, whereupon it will be found that the active chloro- I plastic complex Will largely havebeen adsorbed by the calcium carbonate and this light yellow-colored tritur'ate can be employed exactly as in previous instances. 7 quantity of such triturate to be used in' any specific case can only be determined bya chemical analysis of said A point of distinction between the present invention and my previous invention lies in the state of insolubility' of the chlorophyll and'in the intimate contact of the or'-' ganic medium with each factor of the complex, exactly as present in the green leaf. In line with earlier patent it is perfectly possible to introduce in .an inert adsorbent a solubilized chlorophyllin, followed with' any one or more of the carotenoid.class; this association, however,
lends only a modicum ofprotection to the chlorophyllin', as when. once separated from its congeners and concomitants, it never again is capable of, resisting for any,
The
length of time the destructive action of oxygen and heat. Thus, too, solubilized chlorophyllin does not surrender its bleeding out properties as when paper so treated comes in contact with the mouth.
I claim:
1. A method of enhancing the smoking quality of cigarettes which comprises impregnating the paper Wrapper thereof with an insoluble earth metal hydroxide or carbonate adsorbent carrying a water-insoluble chloroplastic complex as directly securable from chloroplasts of green leaves, the quantity of said complex not exceeding substantially 2% of the dry weight of the cigarette wrapper.
2. A method of enhancing the smoking quality of cigarettes which comprises impregnating the paper wrapper thereof with precipitated calcium carbonate previously triturated with a water-insoluble chloroplastic complex as directly derived from green leaves, the quantity of said complex comprising between approximately of 1% to about 2% of the weight of the paper.
3. An article of manufacture including a triturate comprising an inert refractory inorganic adsorbent and a water-insoluble chloroplastic complex derived from green leaves, and an organic medium chosen from the group consisting of cellulose and tobacco, said triturate being interspersed with said organic medium to facilitate the combustive oxidation of the latter and its decomposition products.
4. An article of manufacture comprising a triturate including an inert refractory organic adsorbent and a Water insoluble chloroplastic complex derived directly from green leaves, and an organic medium interspersed with said triturate, said organic medium being chosen from the group consisting of purified cellulose and tobacco, whereby said organic medium will undergo speedier and more complete combustive oxidation due to the presence of said complex.
5. A method of effecting fuller oxidation of an organic medium, chosen from the group consisting of purified cellulose and tobacco, in the presence of air, comprising the step of interspersion in said organic medium of a triturate of a refractory inorganic adsorbent with a water-insoluble chloroplastic complex.
6. A cigarette comprising shredded tobacco and a paper 6 wrapper, means interspersed throughout said tobacco and wrapper to effect fuller oxidation thereof, said means including an inert inorganic adsorbent and a water-insoluble chloroplastic complex adsorbed within said adsorbent, the quantity of said complex per se not exceeding substantially 2% of the dry weight of the cigarette.
7. A cigarette paper including 10% to 25% of its Weight of an adsorbent selected from the group comprising insoluble earth metal hydroxides and insoluble earth metal carbonates, and a Water-insoluble chloroplastic complex directly derived from green leaves; said complex being carried by said adsorbent and said complex being present in an amount not exceeding substantially 2% of the dry weight of the paper.
8. As an article of manufacture, thin cellulosic sheets adapted for use as cigarette paper comprising an adsorbent selected from the group comprising insoluble earth metal hydroxides, and insoluble earth metal carbonates having incorporated therewith as a triturate a chloroplastic complex derived directly from green leaves, said complex being present in an amount not more than substantially 2% of the dry weight of the paper.
References Cited in the file of this patent UNITED STATES PATENTS 1,462,480 Bosse July 24, 1923 1,581,618 Sulzberger Apr. 20, 1926 1,638,700 Molofsky Aug. 9, 1927 1,842,266 Hicks Ian. 19, 1932 1,870,259 McKee Aug/9, 1932 2,188,319 Sierners Jan. 30, 1940 2,305,828 Kuhn Dec. 22, 1942 2,333,658 Mattill et al. Nov. 9, 1943 2,349,590 Hickman May 23, 1944 2,433,593 Buxton Dec. 30, 1947 2,460,284 Hale I Feb. 1, 1949 2,460,285 Hale I1 Feb. 1, 1949 2,493,288 Hall Jan. 3, 1950 2,513,002 Chenicek June 27, 1950 2,567,362 Berkman et al. Sept. 11, 1951 FOREIGN PATENTS 485,188 Great Britain May 13, 1938

Claims (1)

1. A METHOD OF ENCHANCING THE SMOKING QUALITY OF CIGARETTES WHICH COMPRISES IMPREGNATING THE PAPER WRAPPER THEREOF WITH AN INSOLUBLE EARTH METAL HYDROXIDE OR CARBONATE ADSORBENT CARRYING A WATER-INSOLUBLE CHLOROPLASTIC COMPLEX AS DIRECTLY SECURABLE FROM CHLOROPLASTS OF GREEN LEAVES, THE QUANTITY OF SAID COMPLEX NOT EXCEEDING SUBSTANTIALLY 2% OF THE DRY WEIGHT OF THE CIGARETTE WRAPPER.
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Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3087500A (en) * 1960-10-10 1963-04-30 Jacobson George Cigarette filters
US3106211A (en) * 1957-11-18 1963-10-08 Reynolds Metals Co Tobacco product
US3112754A (en) * 1961-10-30 1963-12-03 Robert Harper J Method of making a tobacco substtute
US3312226A (en) * 1964-02-26 1967-04-04 Philip Morris Inc Smoking tobacco composition
US3339558A (en) * 1966-10-28 1967-09-05 Haskett Barry F Smoking article and filter therefor containing vitamin a
US3656489A (en) * 1969-08-26 1972-04-18 Eldon Stahly Method of treating tobacco smoke to eliminate metal carbonyl content thereof
US3667478A (en) * 1969-07-17 1972-06-06 Nelson J Waterbury Filter cigarette incorporating vitamin a

Citations (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1462480A (en) * 1920-09-17 1923-07-24 Frederick J Bosse Smoking mixture
US1581618A (en) * 1921-04-30 1926-04-20 Sulzberger Nathan Paper
US1638700A (en) * 1926-10-23 1927-08-09 Silmo Chemical Company Inc Fish-oil product and method of making the same
US1842266A (en) * 1931-04-14 1932-01-19 Calvin S Hicks Toracco mixture
US1870259A (en) * 1929-03-14 1932-08-09 Ralph H Mckee Paper and process of manufacturing the same
GB485188A (en) * 1935-08-14 1938-05-13 Gerhard Madaus Process for obtaining dry stable therapeutic preparation containing the volatile constituents of freshly gathered plants
US2188319A (en) * 1937-05-28 1940-01-30 Mckesson & Robbins Inc Adsorbate and method of making the same
US2305828A (en) * 1937-03-23 1942-12-22 Kuhn Alfred Dry trituration
US2333658A (en) * 1942-06-22 1943-11-09 Lever Brothers Ltd Antioxidant for fats and oils
US2349590A (en) * 1941-11-06 1944-05-23 Distillation Products Inc Tocopherol-containing composition and process of preparation
US2433593A (en) * 1943-11-19 1947-12-30 Nopco Chem Co Antioxidants and method of producing same
US2460285A (en) * 1944-08-01 1949-02-01 Nat Agrol Company Inc Tobacco products and method of making them
US2460284A (en) * 1944-08-01 1949-02-01 Nat Agrol Company Inc Tobacco composition and method of making it
US2493288A (en) * 1950-01-03 Synergistic antioxhjants anx the
US2513002A (en) * 1947-03-27 1950-06-27 Universal Oil Prod Co Stabilization of crops
US2567362A (en) * 1945-05-03 1951-09-11 Sophia S Berkman Method of extracting pigments from plants

Patent Citations (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2493288A (en) * 1950-01-03 Synergistic antioxhjants anx the
US1462480A (en) * 1920-09-17 1923-07-24 Frederick J Bosse Smoking mixture
US1581618A (en) * 1921-04-30 1926-04-20 Sulzberger Nathan Paper
US1638700A (en) * 1926-10-23 1927-08-09 Silmo Chemical Company Inc Fish-oil product and method of making the same
US1870259A (en) * 1929-03-14 1932-08-09 Ralph H Mckee Paper and process of manufacturing the same
US1842266A (en) * 1931-04-14 1932-01-19 Calvin S Hicks Toracco mixture
GB485188A (en) * 1935-08-14 1938-05-13 Gerhard Madaus Process for obtaining dry stable therapeutic preparation containing the volatile constituents of freshly gathered plants
US2305828A (en) * 1937-03-23 1942-12-22 Kuhn Alfred Dry trituration
US2188319A (en) * 1937-05-28 1940-01-30 Mckesson & Robbins Inc Adsorbate and method of making the same
US2349590A (en) * 1941-11-06 1944-05-23 Distillation Products Inc Tocopherol-containing composition and process of preparation
US2333658A (en) * 1942-06-22 1943-11-09 Lever Brothers Ltd Antioxidant for fats and oils
US2433593A (en) * 1943-11-19 1947-12-30 Nopco Chem Co Antioxidants and method of producing same
US2460285A (en) * 1944-08-01 1949-02-01 Nat Agrol Company Inc Tobacco products and method of making them
US2460284A (en) * 1944-08-01 1949-02-01 Nat Agrol Company Inc Tobacco composition and method of making it
US2567362A (en) * 1945-05-03 1951-09-11 Sophia S Berkman Method of extracting pigments from plants
US2513002A (en) * 1947-03-27 1950-06-27 Universal Oil Prod Co Stabilization of crops

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3106211A (en) * 1957-11-18 1963-10-08 Reynolds Metals Co Tobacco product
US3087500A (en) * 1960-10-10 1963-04-30 Jacobson George Cigarette filters
US3112754A (en) * 1961-10-30 1963-12-03 Robert Harper J Method of making a tobacco substtute
US3312226A (en) * 1964-02-26 1967-04-04 Philip Morris Inc Smoking tobacco composition
US3339558A (en) * 1966-10-28 1967-09-05 Haskett Barry F Smoking article and filter therefor containing vitamin a
US3667478A (en) * 1969-07-17 1972-06-06 Nelson J Waterbury Filter cigarette incorporating vitamin a
US3656489A (en) * 1969-08-26 1972-04-18 Eldon Stahly Method of treating tobacco smoke to eliminate metal carbonyl content thereof

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