US3802441A - Tobacco smoke filter additive - Google Patents
Tobacco smoke filter additive Download PDFInfo
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- US3802441A US3802441A US00220743A US22074372A US3802441A US 3802441 A US3802441 A US 3802441A US 00220743 A US00220743 A US 00220743A US 22074372 A US22074372 A US 22074372A US 3802441 A US3802441 A US 3802441A
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- zinc oxide
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- carbonate
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
- B01J20/28—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof characterised by their form or physical properties
- B01J20/28014—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof characterised by their form or physical properties characterised by their form
- B01J20/28033—Membrane, sheet, cloth, pad, lamellar or mat
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- A—HUMAN NECESSITIES
- A24—TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
- A24D—CIGARS; CIGARETTES; TOBACCO SMOKE FILTERS; MOUTHPIECES FOR CIGARS OR CIGARETTES; MANUFACTURE OF TOBACCO SMOKE FILTERS OR MOUTHPIECES
- A24D3/00—Tobacco smoke filters, e.g. filter-tips, filtering inserts; Filters specially adapted for simulated smoking devices; Mouthpieces for cigars or cigarettes
- A24D3/06—Use of materials for tobacco smoke filters
- A24D3/16—Use of materials for tobacco smoke filters of inorganic materials
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
- B01J20/28—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof characterised by their form or physical properties
- B01J20/28014—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof characterised by their form or physical properties characterised by their form
- B01J20/28023—Fibres or filaments
Definitions
- a cigarette or other tobacco smoke filter which has a filamentary or fibrous cellulose acetate support carrying a stabilized mixture of zinc oxide and an alkali carbonate salt.
- the zinc oxide and the carbonate salt are dispersed in a plasticizer to form the stabilized mixture by a milling operation.
- the invention is directed to improvements relating to filters for tobacco smoke.
- the filters are intended for use attached either to' cigarettes, cigars, or cigarillos, or as a separate cartridge filter for pipes, cigarettes, or cigar holders. Further, the filters may be employed attached to smoking articles formed from reconstituted tobacco.
- tobacco smoke consists of a gaseous or vapor phase in which are suspended liquid or semi-liquid droplets or solid particles, which form the visible smoke stream.
- Conventional cigarette filters are formed from cellulosic fibers or convoluted creped paper formed into a cylindrical plug to remove varying proportions of the droplets passing therethrough. For the most part, they do not effectively remove gaseous molecules.
- Such gaseous molecules including hydrogen cyanide and hydrogen sulfide can be considered as gases or highly volatile liquids. ln the brief period of time in which they are carried from the tobacco combustion zone to the smokers mouth, there is relatively little time for the gases to condense into droplets. Consequently, these materials are almost entirely found in the vaporized state as they leave the smoking article and enter the smokers mouth.
- the smooth and generally non-porous nature of commonly used fibrous filtering materials may capture tobacco smoke droplets, but do not present a sufficient surface area to effectively adsorb gaseous molecules.
- a primary object of the present invention to provide an improved filter additive adapted to be combined with a filter material for removing substantial quantities of volatile constituents, particularly hydrogen cyanide and hydrogen sulfide from the smoke of burning tobacco.
- a tobacco smoke filter comprising a support or carrier of fibrous, filamentary or sheet filtering material, carrying a mixture comprising zinc oxide and a carbonate salt selected from the group consisting of sodium carbonate, potassium carbonate or mixtures thereof.
- a carbonate salt selected from the group consisting of sodium carbonate, potassium carbonate or mixtures thereof.
- Such filter may be connected at one end to an outer wrapper having a charge of tobacco therein.
- To produce the filter a stable suspension of zinc oxide, sodium or potassium carbonate and a liquid plasticizer is formed and the suspension is thereafter sprayed on the filter support.
- FIG. 1 is a graph illustrating the unexpected selective filtration property with respect to hydrogen cyanide, of the filter of the invention
- FIG. 2 is a graph depicting the unexpected selective filtration characteristic with respect to hydrogen sulfide, of the filter of the invention.
- FIG. 3 is a graph illustrating the unexpected selective filtration properties with respect to hydrogen cyanide of the improved filter material as compared to expected efficiencies for predetermined loadings of additive.
- the tobacco smoke filter of the invention is produced by treating a tobacco smoke filtering material formed from, for example, fibrous, filamentary or sheet material with a mixture of zinc oxide and either sodium carbonate, potassium carbonate or mixtures thereof.
- a tobacco smoke filtering material formed from, for example, fibrous, filamentary or sheet material with a mixture of zinc oxide and either sodium carbonate, potassium carbonate or mixtures thereof.
- a stable suspension of the mixture is formed.
- the stable suspension is formed by intimately combining, with agitation, zinc oxide and sodium carbonate solids and a liquid plasticizer.
- liquid plasticizers may be employed such as: triethylene glycol diacetate, triethylene citrate, triacetin, and glycerol derivatives.
- the concentration of solids in the dispersed plasticizer is from about lOto 40 per cent of the combined weight of the solids and plasticizer.
- the additive solids and liquid plasticizer are introduced into a ball mill, and milled for a sufficient period of time to form a sprayable dispersion stable for at least four to five days.
- the milling step is carried on for at least about 16 hours to insure that a sufficiently reduced solids particle size is obtained.
- the stable additive plasticizer dispersion permits both deposition of the additive on tobacco smoke filter material, such as conventional cellulose acetate tow, and also simultaneous addition of a plasticizer to the tow, which causes a fiber-to-fiber bond to form.
- tobacco smoke filter material such as conventional cellulose acetate tow
- plasticizer to the tow
- organic water-soluble zinc acetate and sodium acetate salts were added to creped paper in an aqueous solution. It is a feature of the present invention that a stable, sprayable dispersion containing a filter additive and a plasticizer is applied to conventional cellulose acetate tow, both to enhance the selective filtration properties of the resulting filter, and also to provide a strengthened and more resilient filter as a result of the plasticizing action of the dispersion.
- the molar ratio of zinc oxide to sodium and/or potassium carbonate in the additive mixture may be varied widely, nevertheless, the described ranges are deemed to be most practical and efficient.
- the molar ratio of zinc oxide to sodium and /or potassium carbonate in the filter additive is from about 25:1 to 1:25.
- Enhanced selective removal characteristics are obtained when the molar ratio of zinc oxide to sodium carbonate is from about 8:1 to 1:5 as is shown by FIG. 3.
- B Amount of hydrogen cyanide left after acetate filtration.
- C Amount of hydrogen cyanide left after zinc oxide filtration.
- D Amount of hydrogen cyanide delivered smoker, after sodium carbonate filtration.
- E; E;, E] E,,, E E are parameters which account for the fact that what is filtered by one component cannot be removed by the other components.
- FIG. No. 3 also shows why the molar ratio range of 8:1 to 1:5, zinc oxide to sodium carbonate, is preferred. Obtaining a filter efficiency of percent and more is simple. One merely adds sufficient zinc oxide and sodium carbonate to stay above and right of the 80 percent contour.
- FIG. 3 shows the greatest separation of the 50 percent and 80 percent contours when the above molar ratios are within 8:] to 1:5.
- a 1% variation in additive amount or ratio causes relatively small changes in total filter efficiency in the preferred molar ratio range.
- a 1 percent variation outside the preferred range results in greater variations in efficiency.
- the preferred molar ratio range allows better control over the 50 percent 80 percent filter efficiency range.
- sufficient zinc oxide and sodium and/or potassium carbonate are employed in the tobacco smoke filter to provide from about 2 to 25 milligrams (mgs.) of solids mixture per cigarette. It is particularly preferred to employ from about 3 to 10 mgs. of the zinc oxide-sodium carbonate mixture per cigarette. As illustrated in FIG. 3, generally at least about 30 micromoles of additive are preferably employed in a filter section.
- the above-described, bloomed, tow was then sprayed using a conventional laboratory atomizer with a stable dispersion formed by milling a mixture of 200 grams of zinc oxide, 50 grams sodium carbonate and 550 grams of plasticizer for 24 hours.
- the molar ratio of zinc oxide to sodium carbonate in the dispersion was 5:1.
- the plasticizer employed was a mixture of 6 parts by weight triethylene glycol diacetate and 5 parts by weight polyethylene glycol.
- the sprayed tow was then gathered, and placed into the tobacco cavity of a manual cigarette making machine.
- the cigarette-maker employed was the revolutionary LAREDO cigarette-maker, described in U.S. Pat. No. 3,491,768 issued Jan. 27, I970.
- the filter-rod of the invention was fabricated as one would fabricate a cigarette in the LAREDO cigarette-maker.
- the resulting rods were cured for at least four hours, and thereafter severed into 21 mm. segments.
- the 21 mm. filters were inserted in the tipping cavity of a standard 84 mm. cigarette.
- Cigarettes made by the above procedures were smoked mechanically, using a conventional smoking machine which smoked the cigarettes to tipping plus 3 mm., employing FTC procedures.
- the filters fabricated by the above procedures contained 4 mgs. of zinc oxide and 0.9 mgs. of sodium carbonate.
- the proportions of hydrogen cyanide and hydrogen sulfide removed from the smoke were determined by standard analytical methods.
- EXAMPLE II rods were formed into cigarettes, and tested according to the procedure of Example I.
- the results of the tests are illustrated in the graphs of I FIGS. 1 and 2.
- the weight per cent of cyanide or sulfide removed [as compared to untreated smoke] is plotted against weight loading in milligrams of zinc oxide and/or sodium carbonate in the filter section.
- typical removal levels for hydrogen cyanide by zinc oxide range from 23 to 58 per cent, while the removal levels for sodium carbonate range from 48 to 62 per cent.
- the expected additive effects of a filter section contain ing equal loadings by weight of zinc oxide and sodium carbonate is represented by a median line. Since the Gram Molecular Weight for zinc oxide and sodium carbonate is almost identical, the graph also represents the expected smoke selective removal properties at equimolar concentrations.
- the actual removal efficiency for the filter additive with respect to hydrogen cyanide was over 30 per cent greater than the expected additive result.
- the theory behind the synergistic interaction is not presently understood. It is postulated, however, that the more uniform deposition of finely divided additive on the filter section provided by the stable dispersion initially formed is at least partially responsible. However, dusted mixtures of additive have yielded somewhat unexpected selective removal efficiencies also.
- the actual removal efficiency with respect to hydrogen sulfide is found to be per cent better than that expected by the combination of individual ingredients.
- EXAMPLE IV A stable dispersion of 73.5 parts plasticizer, 19.8 parts zinc oxide and 6.8 parts potassium carbonate (parts by weight) was formed in accordance with the procedures set forth in Example I.
- Filters containing 6 mg of zinc oxide and 2 mg of potassium carbonate (molar ratio of 4.4/1) were formed and tested as per Example 1.
- the removal efficiencies, 73% for HCN and 82% for H S, are comparable to an equivalent zinc oxide/sodium carbonate treated filter.
- COMPARATIVE EXAMPLE I A stable dispersion of 74.8 parts plasticizer, 20.2 parts zinc oxide and 5.0 parts calcium carbonate was formed and tested as per Example 1. Filters containing 6 mg zinc oxide and 1.6 mg calcium carbonate (molar ratio of 4.6/1 were substantially ineffective for removing hydrogen cyanide or hydrogen sulfide. Selective removal efficiencies for hydrogen cyanide and hydrogen sulfide were 22% and 12% respectively.
- COMPARATIVE EXAMPLE II A stable dispersion of 74.6 parts plasticizer, 20.3 parts zinc oxide and 5.1 parts magnesium carbonate were formed and tested according to Example 1. Filters containing 6 mg zinc oxide and 1.5 mg of magnesium carbonate (molar ratio of 4.1/1 were not effective for removing hydrogen cyanide or hydrogen sulfide with removal efficiencies of 28% and 2% respectively.
- An improved tobacco smoke filter comprising a carrier of fibrous or filamentary cellulose acetate on which is supported a stabilized mixture comprising a plasticizer, zinc oxide and a carbonate salt selected from the group consisting of sodium carbonate. potassium carbonate or mixtures thereof; and said molar ratio of zinc oxide to said carbonate salt being from about 25 to l to l to 25, said mixture resulting from the intimate dispersion of said zinc oxide and carbonate salt in said plasticizer by a milling operation.
- a smoking article comprising a charge of tobacco enrobed in an outer wrapper and a filter connected to one end of said wrapper, wherein said filter comprises a carrier of fibrous or filamentary cellulose acetate on which is supported a stabilized mixture comprising a plasticizer, zinc oxide and a carbonate salt selected from the group consisting of potassium carbonate, sodium carbonate or mixtures thereof, and said molar ratio of said zinc oxide to said carbonate salt being from about 25 to l to l to 25, said mixture resulting from the intimate dispersion of said zinc oxide and carbonate salt in said plasticizer by a milling operation.
- said mixture comprises from about 90 to 60 percent by weight liquid plasticizer and from about 10 to 40 percent by weight of said mixture of zinc oxide and carbonate salt, said weights based on the combined weight of said mixture and plasticizer.
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- Analytical Chemistry (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Inorganic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
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Abstract
A cigarette or other tobacco smoke filter is disclosed which has a filamentary or fibrous cellulose acetate support carrying a stabilized mixture of zinc oxide and an alkali carbonate salt. The zinc oxide and the carbonate salt are dispersed in a plasticizer to form the stabilized mixture by a milling operation.
Description
United States Patent 1 Hammersrnith TOBACCO SMOKE FILTER ADDITIVE [75] Inventor: James R. Hammer-smith,
Jeffersonville, Ind.
[73] Assignee: Brown & Williamson Tobacco Corporation, Louisville, Ky.
[22] Filed: Jan. 26, 1972 [21] Appl. No.: 220,743
[52] US. Cl 131/109, 131/267, 131/266 51 Int. Cl, A24b /02 [58] Field of Search 131/261-269,
l3l/10l0.9, 17, 140
[56] References Cited UNITED STATES PATENTS 2/1969 Sublett et a1 131/266 11/1965 Spears et a1. 131/266 Z/IYC OXIDE EXPECTED ms/wwz 1451 Apr. 9, 1974 3,021,242 2/1962 Touey 131/266 X 3,550,600 12/1970 Horsewell et a1. 131/267 3,251,365 5/1966 Keith et a1. 131/109 X 3,618,619 11/1971 Kiefer 131/266 X 3.426.763 2/1969 Sloan et a1. 131/266 Primary ExaminerMelvin D. Rein Attorney, Agent, or Firm-Finnegan, Henderson, Farabow & Garrett [5 7 ABSTRACT A cigarette or other tobacco smoke filter is disclosed which has a filamentary or fibrous cellulose acetate support carrying a stabilized mixture of zinc oxide and an alkali carbonate salt. The zinc oxide and the carbonate salt are dispersed in a plasticizer to form the stabilized mixture by a milling operation.
7 Claims, 3 Drawing Figures l 1 l 1 l PATENTEDAPR 91914 3,802,441
saw 3 er 3 X X EXPERIMENTAL EFF/(VE/VC) TOBACCO SMOKE FILTER ADDITIVE BACKGROUND OF THE INVENTION The invention is directed to improvements relating to filters for tobacco smoke. The filters are intended for use attached either to' cigarettes, cigars, or cigarillos, or as a separate cartridge filter for pipes, cigarettes, or cigar holders. Further, the filters may be employed attached to smoking articles formed from reconstituted tobacco.
As is well known, tobacco smoke consists of a gaseous or vapor phase in which are suspended liquid or semi-liquid droplets or solid particles, which form the visible smoke stream. Conventional cigarette filters are formed from cellulosic fibers or convoluted creped paper formed into a cylindrical plug to remove varying proportions of the droplets passing therethrough. For the most part, they do not effectively remove gaseous molecules. t I
Such gaseous molecules, including hydrogen cyanide and hydrogen sulfide can be considered as gases or highly volatile liquids. ln the brief period of time in which they are carried from the tobacco combustion zone to the smokers mouth, there is relatively little time for the gases to condense into droplets. Consequently, these materials are almost entirely found in the vaporized state as they leave the smoking article and enter the smokers mouth. The smooth and generally non-porous nature of commonly used fibrous filtering materials may capture tobacco smoke droplets, but do not present a sufficient surface area to effectively adsorb gaseous molecules.
In an attempt to improve the adsorptive properties of conventional tobacco smoke filters, various adsorbents have been proposed for ordinary filtering materials. In U. S. Pats. No. 3,251,365 and 3,460,543, it is disclosed that zinc oxide particles may'be added to a filter for a smoking article. However, zinc oxide particles, per se, are not efficient in removing gaseous components, particularly hydrogen cyanide and hydrogen sulfide from tobacco smoke, except at unacceptably high levels.
Various carbonates, including sodium carbonate, are described as being useful to reduce the temperature of burning tobacco in various prior art patents, such as U. S. Pat. No. 3,034,932. Tests have shown, however, that sodium carbonate, magnesium carbonate and calcium carbonate in either the hydrous or anhydrous form, have very limited effectiveness in removing volatile components from smoke, particularly hydrogen cyanide. Sodium carbonate has proven particularly inefficient in removing hydrogen sulfide from tobacco smoke.
In US. Pat. No. 3,550,600 it is disclosed that a mixture of hydrated zinc acetate and sodium acetate removes volatile compounds from tobacco smoke, including hydrogen cyanide and hydrogen sulfide. While the above metal organic salts provide satisfactory selective removal of volatile constituents, there remains an additional need for providing selective removal of volatile smoke constituents, employing inexpensive and readily available additives, such as inorganic salts. It is well known that inorganic salts are difficult to admix with the organic plasticizers commonly employed to deposit additives on cellulose acetate filter material. As illustrated hereinbelow, attempts to substitute sodium carbonate for the sodium acetate of the -600 Patent described above have proved unsatisfactory. Severe reductions in selective removal of gaseous components, particularly hydrogen sulfide are noted.
SUMMARY OF THE INVENTION It is, therefore, a primary object of the present invention to provide an improved filter additive adapted to be combined with a filter material for removing substantial quantities of volatile constituents, particularly hydrogen cyanide and hydrogen sulfide from the smoke of burning tobacco.
It is another object of the invention to provide an im proved filter employing inexpensive additive material for removing volatile or gaseous tobaccosmoke constituents.
The above, and other beneficial objects and advantages are obtained in accordance with the present invention by a tobacco smoke filter comprising a support or carrier of fibrous, filamentary or sheet filtering material, carrying a mixture comprising zinc oxide and a carbonate salt selected from the group consisting of sodium carbonate, potassium carbonate or mixtures thereof. Such filter may be connected at one end to an outer wrapper having a charge of tobacco therein. To produce the filter a stable suspension of zinc oxide, sodium or potassium carbonate and a liquid plasticizer is formed and the suspension is thereafter sprayed on the filter support.
BRIEF DESCRIPTION OF THE DRAWINGS FIG. 1 is a graph illustrating the unexpected selective filtration property with respect to hydrogen cyanide, of the filter of the invention;
FIG. 2 is a graph depicting the unexpected selective filtration characteristic with respect to hydrogen sulfide, of the filter of the invention; and
FIG. 3 is a graph illustrating the unexpected selective filtration properties with respect to hydrogen cyanide of the improved filter material as compared to expected efficiencies for predetermined loadings of additive.
DESCRIPTION OF THE PREFERRED EMBODIMENTS The tobacco smoke filter of the invention is produced by treating a tobacco smoke filtering material formed from, for example, fibrous, filamentary or sheet material with a mixture of zinc oxide and either sodium carbonate, potassium carbonate or mixtures thereof. In order to facilitate application of the additive mixture onto conventinal cigarette filtering material, such as cellulose acetate tow, a stable suspension of the mixture is formed.
Although the following discussion is directed to zinc oxide and sodium carbonate additives, it is also applicable to potassium carbonate and zinc oxide additives and other carbonate and zinc oxide mixtures. In genera], the stable suspension is formed by intimately combining, with agitation, zinc oxide and sodium carbonate solids and a liquid plasticizer. Conventional liquid plasticizers may be employed such as: triethylene glycol diacetate, triethylene citrate, triacetin, and glycerol derivatives.
For practical use, generally, the concentration of solids in the dispersed plasticizer is from about lOto 40 per cent of the combined weight of the solids and plasticizer. In preparing the stable suspension, the additive solids and liquid plasticizer are introduced into a ball mill, and milled for a sufficient period of time to form a sprayable dispersion stable for at least four to five days. The milling step is carried on for at least about 16 hours to insure that a sufficiently reduced solids particle size is obtained.
The stable additive plasticizer dispersion permits both deposition of the additive on tobacco smoke filter material, such as conventional cellulose acetate tow, and also simultaneous addition of a plasticizer to the tow, which causes a fiber-to-fiber bond to form. Previously, organic water-soluble zinc acetate and sodium acetate salts were added to creped paper in an aqueous solution. It is a feature of the present invention that a stable, sprayable dispersion containing a filter additive and a plasticizer is applied to conventional cellulose acetate tow, both to enhance the selective filtration properties of the resulting filter, and also to provide a strengthened and more resilient filter as a result of the plasticizing action of the dispersion.
Although the molar ratio of zinc oxide to sodium and/or potassium carbonate in the additive mixture may be varied widely, nevertheless, the described ranges are deemed to be most practical and efficient. In general, the molar ratio of zinc oxide to sodium and /or potassium carbonate in the filter additive is from about 25:1 to 1:25. Enhanced selective removal characteristics are obtained when the molar ratio of zinc oxide to sodium carbonate is from about 8:1 to 1:5 as is shown by FIG. 3.
The following discussion demonstrates the unpredicted selective removal efficiencies obtained with the tobacco smoke filter of the invention. The expected filter efficiency for hydrogen cyanide is derived as follows:
where E,= Fractional efficiency of acetate tow only.
E Fractional efficiency of zinc oxide only. E,, Fractional efficiency of sodium carbonate only.
A Amount of hydrogen cyanide presented to the filter. B Amount of hydrogen cyanide left after acetate filtration. C Amount of hydrogen cyanide left after zinc oxide filtration. D Amount of hydrogen cyanide delivered smoker, after sodium carbonate filtration. Considering that which is filtered by one component cannot be filtered by the other component, the following is derived:
1. D=A(1-E,)=C(1E,,)
=A(1- Er)(l E,) (131 En) l E: n) f z n' f Z f n Z Therefore, the total filter efficiency, E,, is: 11. E, E,+ E, E, E,E,E,, E,E E E,, E E
to the EfEzEn is the term for interaction which increases overall filtration performance when all three components are present.
E; E;, E] E,,, E E" are parameters which account for the fact that what is filtered by one component cannot be removed by the other components.
Since E, is a mechanical filtration, it is assumed that E is a constant independent of the chemical filtration, E and E Thus values for only E, or E are found from the equation:
where t z or n and E, is the total filtration with z or n.
Once the values for E and E, versus the amount of zinc oxide and sodium carbonate are known, then total efficiency contours can be plotted for any mixture on the filter. This is shown in FIG. No. 3. The experimental E E E, term has been found to be much greater than predicted and the total filtration efficiency is raised proportional to [(E E E experimental (E,E E,,) calculated].
FIG. No. 3 also shows why the molar ratio range of 8:1 to 1:5, zinc oxide to sodium carbonate, is preferred. Obtaining a filter efficiency of percent and more is simple. One merely adds sufficient zinc oxide and sodium carbonate to stay above and right of the 80 percent contour.
Controlling the filter efficiency between 50 percent and 80 percent is difficult. FIG. 3 shows the greatest separation of the 50 percent and 80 percent contours when the above molar ratios are within 8:] to 1:5. A 1% variation in additive amount or ratio causes relatively small changes in total filter efficiency in the preferred molar ratio range. A 1 percent variation outside the preferred range results in greater variations in efficiency. Thus, the preferred molar ratio range allows better control over the 50 percent 80 percent filter efficiency range.
Furthermore, with regard to filter efficiences beyond the 25:1 to 1:25 molar ratio range, the required amount of mixture is near the predicted requirements. Within the 25:1 to 1:25 molar ratio range, high efficiencies are achieved with much reduced amounts of additive on the filter tow.
In general, sufficient zinc oxide and sodium and/or potassium carbonate are employed in the tobacco smoke filter to provide from about 2 to 25 milligrams (mgs.) of solids mixture per cigarette. It is particularly preferred to employ from about 3 to 10 mgs. of the zinc oxide-sodium carbonate mixture per cigarette. As illustrated in FIG. 3, generally at least about 30 micromoles of additive are preferably employed in a filter section.
Comparative tests with mixtures of zinc oxide and calcium or magnesium carbonate illustrate the criticality of employing Group IA metal carbonates. Selective removal efficiencies for hydrogen cyanide and hydrogen sulfide were only a fraction of those obtained with Group 1A metal carbonates, especially sodium and potassium carbonate.
The following examples are illustrative only, and are not limitive of scope:
EXAMPLE I In order to demonstrate the efficiency with which the improved filter selectively removes volatile smoke constituents, particularly hydrogen cyanide and hydrogen sulfide, a 30 centimeter (cm.) length of unbloomed 3.3Y-44,000 cellulose acetate tow was bloomed by hand. The end of the tow was squared, and 6- centimeter lengths were cut off. The tow weights were adjusted by end-trimming to 400 mgs.
The above-described, bloomed, tow was then sprayed using a conventional laboratory atomizer with a stable dispersion formed by milling a mixture of 200 grams of zinc oxide, 50 grams sodium carbonate and 550 grams of plasticizer for 24 hours. The molar ratio of zinc oxide to sodium carbonate in the dispersion was 5:1. The plasticizer employed was a mixture of 6 parts by weight triethylene glycol diacetate and 5 parts by weight polyethylene glycol.
The sprayed tow was then gathered, and placed into the tobacco cavity of a manual cigarette making machine. The cigarette-maker employed was the revolutionary LAREDO cigarette-maker, described in U.S. Pat. No. 3,491,768 issued Jan. 27, I970. The filter-rod of the invention was fabricated as one would fabricate a cigarette in the LAREDO cigarette-maker. The resulting rods were cured for at least four hours, and thereafter severed into 21 mm. segments. The 21 mm. filters were inserted in the tipping cavity of a standard 84 mm. cigarette.
Cigarettes made by the above procedures were smoked mechanically, using a conventional smoking machine which smoked the cigarettes to tipping plus 3 mm., employing FTC procedures.
The filters fabricated by the above procedures contained 4 mgs. of zinc oxide and 0.9 mgs. of sodium carbonate. The proportions of hydrogen cyanide and hydrogen sulfide removed from the smoke were determined by standard analytical methods.
Analysis of the tobacco smoke shows an 80 per cent reduction of hydrogen cyanide, and an 89 percent reduction of hydrogen sulfide, as compared to a control filter-rod fabricated by the above procedures, but
formed without the filter additive.
EXAMPLE II rods were formed into cigarettes, and tested according to the procedure of Example I.
The results of the tests are illustrated in the graphs of I FIGS. 1 and 2. The weight per cent of cyanide or sulfide removed [as compared to untreated smoke] is plotted against weight loading in milligrams of zinc oxide and/or sodium carbonate in the filter section. As illustrated in FIG. 1, typical removal levels for hydrogen cyanide by zinc oxide range from 23 to 58 per cent, while the removal levels for sodium carbonate range from 48 to 62 per cent. As further illustrated in FIG. 1, the expected additive effects of a filter section contain ing equal loadings by weight of zinc oxide and sodium carbonate is represented by a median line. Since the Gram Molecular Weight for zinc oxide and sodium carbonate is almost identical, the graph also represents the expected smoke selective removal properties at equimolar concentrations.
As seen in FIG. 1, the actual removal efficiency for the filter additive with respect to hydrogen cyanide was over 30 per cent greater than the expected additive result. The theory behind the synergistic interaction is not presently understood. It is postulated, however, that the more uniform deposition of finely divided additive on the filter section provided by the stable dispersion initially formed is at least partially responsible. However, dusted mixtures of additive have yielded somewhat unexpected selective removal efficiencies also. As depicted in FIG. 2, the actual removal efficiency with respect to hydrogen sulfide is found to be per cent better than that expected by the combination of individual ingredients. Again, while the nature of the interaction between the additives is not presently understood, it is postulated that the uniform fine particle dispersion formed allows a more uniform deposition of additive on the filter plug, resulting in a greater surface area of particles presented to the tobacco smoke stream passing therethrough. Prior art methods of introducing solid particles onto filter plugs tended to produce aggregates or agglomerates thereon, thus reducing the surface area of the particles and their selective removal efficiency.
The data graphically presented in FIGS. 1 and 2 is presented in tabular form in Table 1.
TABLE I Synergism of Zinc Oxide/Sodium Carbonate Removal Efficiencies Amount Per Filter Additive mg micro moles HCN H 8 Zinc Oxide 2.l 26 23 Sodium Carbonate 3.2 30 48 8 Zinc Oxide/Sodium 3.8/0.2 47/2 63 54 Carbonate 4.0/0.9 49/9 89 EXAMPLE III In U.S. Pat. No. 3,550,600 there are presented data showing satisfactory properties of a filter formed from zinc acetate and sodium acetate. A test was conducted substituting sodium carbonate monohydrate for the sodium acetate. The filters were formed, attached to the cigarettes, and smoked as described in U.S. Pat. No. 3,550,600. Table 2 summarizes theresults obtained.
i" TABLE 2 Wt. each Smoke Component component removed Test Run Additive I in filter HCN H 3 1. zinc acetate 1 5 60 82 sodium acetate 5 2. zinc acetate 5 62 2] 3 sodium carbonate 5 53 9 monohydrate zinc acetate 5 The results indicate that the substitution of sodium carbonate for sodium acetate causes a 71 percent drop in selective removal efficiency with respect to hydrogen sulfide, and a 7 percent drop with respect to hydrogen cyanide. Notwithstanding the adverse test results, it has been discovered that the further substitution of zinc oxide for zinc acetate provides unexpectedly enfor hydrogen cyanide, and 70 percent for hydrogen sulfide.
EXAMPLE IV A stable dispersion of 73.5 parts plasticizer, 19.8 parts zinc oxide and 6.8 parts potassium carbonate (parts by weight) was formed in accordance with the procedures set forth in Example I.
Filters containing 6 mg of zinc oxide and 2 mg of potassium carbonate (molar ratio of 4.4/1) were formed and tested as per Example 1. The removal efficiencies, 73% for HCN and 82% for H S, are comparable to an equivalent zinc oxide/sodium carbonate treated filter.
COMPARATIVE EXAMPLE I A stable dispersion of 74.8 parts plasticizer, 20.2 parts zinc oxide and 5.0 parts calcium carbonate was formed and tested as per Example 1. Filters containing 6 mg zinc oxide and 1.6 mg calcium carbonate (molar ratio of 4.6/1 were substantially ineffective for removing hydrogen cyanide or hydrogen sulfide. Selective removal efficiencies for hydrogen cyanide and hydrogen sulfide were 22% and 12% respectively.
COMPARATIVE EXAMPLE II A stable dispersion of 74.6 parts plasticizer, 20.3 parts zinc oxide and 5.1 parts magnesium carbonate were formed and tested according to Example 1. Filters containing 6 mg zinc oxide and 1.5 mg of magnesium carbonate (molar ratio of 4.1/1 were not effective for removing hydrogen cyanide or hydrogen sulfide with removal efficiencies of 28% and 2% respectively.
This invention is not to be limited except as set forth in the following claims.
Having thus described my invention, what is claimed is:
1. An improved tobacco smoke filter comprising a carrier of fibrous or filamentary cellulose acetate on which is supported a stabilized mixture comprising a plasticizer, zinc oxide and a carbonate salt selected from the group consisting of sodium carbonate. potassium carbonate or mixtures thereof; and said molar ratio of zinc oxide to said carbonate salt being from about 25 to l to l to 25, said mixture resulting from the intimate dispersion of said zinc oxide and carbonate salt in said plasticizer by a milling operation.
2. The invention in accordance with claim 1, in which the molar ratio of zinc oxide to sodium carbonate is from about 8:1 to 1:5.
3. The invention in accordance with claim 1 in which said mixture comprises from about to 60 percent by weight liquid plasticizer and from about 10 to 40 percent by weight of said mixture of zinc oxide and carbonate salt, said weights based on the combined weight of said mixture and plasticizer.
4. A smoking article comprising a charge of tobacco enrobed in an outer wrapper and a filter connected to one end of said wrapper, wherein said filter comprises a carrier of fibrous or filamentary cellulose acetate on which is supported a stabilized mixture comprising a plasticizer, zinc oxide and a carbonate salt selected from the group consisting of potassium carbonate, sodium carbonate or mixtures thereof, and said molar ratio of said zinc oxide to said carbonate salt being from about 25 to l to l to 25, said mixture resulting from the intimate dispersion of said zinc oxide and carbonate salt in said plasticizer by a milling operation.
5. The invention in accordance with claim 4 in which the molar ratio of zinc oxide to sodium carbonate is from about 8:1 to 1:5.
6. The invention in accordance with claim 4 wherein at least about 30 micromoles of said mixture is deposited on said filter carrier.
7. The invention in accordance with claim 4 in which said mixture comprises from about 90 to 60 percent by weight liquid plasticizer and from about 10 to 40 percent by weight of said mixture of zinc oxide and carbonate salt, said weights based on the combined weight of said mixture and plasticizer.
Claims (6)
- 2. The invention in accordance with claim 1, in which the molar ratio of zinc oxide to sodium carbonate is from about 8:1 to 1:5.
- 3. The invention in accordance with claim 1 in which said mixture comprises from about 90 to 60 percent by weight liquid plasticizer and from about 10 to 40 percent by weight of said mixture of zinc oxide and carbonate salt, said weights based on the combined weight of said mixture and plasticizer.
- 4. A smoking article comprising a charge of tobacco enrobed in an outer wrapper and a filter connected to one end of said wrapper, wherein said filter comprises a carrier of fibrous or filamentary cellulose acetate on which is supported a stabilized mixture comprising a plasticizer, zinc oxide and a carbonate salt selected from the group consisting of potassium carbonate, sodium carbonate or mixtures thereof, and said molar ratio of said zinc oxide to said carbonate salt being from about 25 to 1 to 1 to 25, said mixture resulting from the intimate dispersion of said zinc oxide and carbonate salt in said plasticizer by a milling operation.
- 5. The invention in accordance with claim 4 in which the molar ratio of zinc oxide to sodium carbonate is from about 8:1 to 1:5.
- 6. The invention in accordance with claim 4 wherein at least about 30 micromoles of said mixture is deposited on said filter carrier.
- 7. The invention in accordance with claim 4 in which said mixture comprises from about 90 to 60 percent by weight liquid plasticizer and from about 10 to 40 percent by weight of said mixture of zinc oxide and carbonate salt, said weights based on the combined weight of said mixture and plasticizer.
Priority Applications (11)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US00220743A US3802441A (en) | 1972-01-26 | 1972-01-26 | Tobacco smoke filter additive |
GB4161672A GB1400197A (en) | 1972-01-26 | 1972-09-07 | Tobacco smoke filter additive |
ZA728844A ZA728844B (en) | 1972-01-26 | 1972-12-14 | Improved tobacco smoke filter |
AU50149/72A AU463557B2 (en) | 1972-01-26 | 1972-12-15 | Improved tobacco smoke filter |
CA159,407A CA959369A (en) | 1972-01-26 | 1972-12-19 | Tobacco smoke filter additive |
DE19722263178 DE2263178C3 (en) | 1972-01-26 | 1972-12-22 | Tobacco smoke filters |
FI3664/72A FI55604C (en) | 1972-01-26 | 1972-12-28 | FILTER FOER TOBAKSROEK |
DK3973AA DK130764B (en) | 1972-01-26 | 1973-01-04 | Filter for tobacco smoke. |
CH80073A CH573719A5 (en) | 1972-01-26 | 1973-01-19 | |
BE794461A BE794461A (en) | 1972-01-26 | 1973-01-24 | IMPROVED FILTER FOR TOBACCO SMOKE |
NL7301195A NL167845C (en) | 1972-01-26 | 1973-01-26 | METHOD FOR MANUFACTURING A FILTER FOR TOBACCO SMOKING AND SMOKE ARTICLES THEREFORE |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US00220743A US3802441A (en) | 1972-01-26 | 1972-01-26 | Tobacco smoke filter additive |
Publications (1)
Publication Number | Publication Date |
---|---|
US3802441A true US3802441A (en) | 1974-04-09 |
Family
ID=22824769
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US00220743A Expired - Lifetime US3802441A (en) | 1972-01-26 | 1972-01-26 | Tobacco smoke filter additive |
Country Status (10)
Country | Link |
---|---|
US (1) | US3802441A (en) |
AU (1) | AU463557B2 (en) |
BE (1) | BE794461A (en) |
CA (1) | CA959369A (en) |
CH (1) | CH573719A5 (en) |
DK (1) | DK130764B (en) |
FI (1) | FI55604C (en) |
GB (1) | GB1400197A (en) |
NL (1) | NL167845C (en) |
ZA (1) | ZA728844B (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20030138497A1 (en) * | 2000-01-14 | 2003-07-24 | Shiseido Co., Ltd. | Inorganic antibacterial/antifungal agents |
EP1541044A1 (en) * | 2002-09-19 | 2005-06-15 | Japan Tobacco Inc. | Filter for cigarette |
US20070224134A1 (en) * | 2006-03-22 | 2007-09-27 | The Procter & Gamble Company | Oral zinc compositions |
EP2130444A1 (en) | 2008-06-06 | 2009-12-09 | Xavier Wertz | Smokable material and smokable articles |
US20170342598A1 (en) * | 2014-12-11 | 2017-11-30 | Solvay Acetow Gmbh | Polymer composition comprising basic additive, process and articles comprising said polymer composition |
WO2018033476A1 (en) * | 2016-08-17 | 2018-02-22 | Philip Morris Products S.A. | Aerosol-generating article having novel tobacco substrate |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4763674A (en) * | 1986-04-16 | 1988-08-16 | Hercules Incorporated | Method and device for controlling hydrogen cyanide and nitric oxide concentrations in cigarette smoke |
EP0250806A3 (en) * | 1986-06-30 | 1988-06-01 | Hercules Incorporated | Method and device for removing nitric oxide from cigarette smoke |
GB201112539D0 (en) | 2011-07-21 | 2011-08-31 | British American Tobacco Co | Porous carbon and methods of production thereof |
Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3021242A (en) * | 1957-12-16 | 1962-02-13 | Eastman Kodak Co | Bonding additives onto filament filters |
US3217719A (en) * | 1962-04-16 | 1965-11-16 | Lorillard Co P | Cigarette filters containing selective adsorbents |
US3251365A (en) * | 1963-03-04 | 1966-05-17 | Ii Charles H Keith | Tobacco smoke filter |
US3426763A (en) * | 1965-07-21 | 1969-02-11 | Eastman Kodak Co | Tobacco smoke filter having a coated carbon additive |
US3428055A (en) * | 1965-04-09 | 1969-02-18 | Eastman Kodak Co | Filter elements and additive therefor |
US3550600A (en) * | 1967-03-29 | 1970-12-29 | Brown & Williamson Tobacco | Cigarette filters |
US3618619A (en) * | 1970-03-03 | 1971-11-09 | Eastman Kodak Co | Tobacco smoke filters |
-
1972
- 1972-01-26 US US00220743A patent/US3802441A/en not_active Expired - Lifetime
- 1972-09-07 GB GB4161672A patent/GB1400197A/en not_active Expired
- 1972-12-14 ZA ZA728844A patent/ZA728844B/en unknown
- 1972-12-15 AU AU50149/72A patent/AU463557B2/en not_active Expired
- 1972-12-19 CA CA159,407A patent/CA959369A/en not_active Expired
- 1972-12-28 FI FI3664/72A patent/FI55604C/en active
-
1973
- 1973-01-04 DK DK3973AA patent/DK130764B/en not_active IP Right Cessation
- 1973-01-19 CH CH80073A patent/CH573719A5/xx not_active IP Right Cessation
- 1973-01-24 BE BE794461A patent/BE794461A/en not_active IP Right Cessation
- 1973-01-26 NL NL7301195A patent/NL167845C/en not_active IP Right Cessation
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3021242A (en) * | 1957-12-16 | 1962-02-13 | Eastman Kodak Co | Bonding additives onto filament filters |
US3217719A (en) * | 1962-04-16 | 1965-11-16 | Lorillard Co P | Cigarette filters containing selective adsorbents |
US3251365A (en) * | 1963-03-04 | 1966-05-17 | Ii Charles H Keith | Tobacco smoke filter |
US3428055A (en) * | 1965-04-09 | 1969-02-18 | Eastman Kodak Co | Filter elements and additive therefor |
US3426763A (en) * | 1965-07-21 | 1969-02-11 | Eastman Kodak Co | Tobacco smoke filter having a coated carbon additive |
US3550600A (en) * | 1967-03-29 | 1970-12-29 | Brown & Williamson Tobacco | Cigarette filters |
US3618619A (en) * | 1970-03-03 | 1971-11-09 | Eastman Kodak Co | Tobacco smoke filters |
Cited By (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20030138497A1 (en) * | 2000-01-14 | 2003-07-24 | Shiseido Co., Ltd. | Inorganic antibacterial/antifungal agents |
EP1541044A1 (en) * | 2002-09-19 | 2005-06-15 | Japan Tobacco Inc. | Filter for cigarette |
US20050161054A1 (en) * | 2002-09-19 | 2005-07-28 | Japan Tobacco Inc. | Cigarette filter |
EP1541044A4 (en) * | 2002-09-19 | 2005-11-16 | Japan Tobacco Inc | Filter for cigarette |
US7487782B2 (en) | 2002-09-19 | 2009-02-10 | Japan Tobacco Inc. | Cigarette filter |
US8778311B2 (en) * | 2006-03-22 | 2014-07-15 | The Procter & Gamble Company | Oral zinc compositions |
US20070224134A1 (en) * | 2006-03-22 | 2007-09-27 | The Procter & Gamble Company | Oral zinc compositions |
EP2130444A1 (en) | 2008-06-06 | 2009-12-09 | Xavier Wertz | Smokable material and smokable articles |
US20170342598A1 (en) * | 2014-12-11 | 2017-11-30 | Solvay Acetow Gmbh | Polymer composition comprising basic additive, process and articles comprising said polymer composition |
CN112375259A (en) * | 2014-12-11 | 2021-02-19 | 索尔维阿塞托有限公司 | Polymer composition comprising basic additive, method and article comprising said polymer composition |
US11352716B2 (en) * | 2014-12-11 | 2022-06-07 | Rhodia Acetow Gmbh | Polymer composition comprising basic additive, process and articles comprising said polymer composition |
CN112375259B (en) * | 2014-12-11 | 2023-10-03 | 索尔维阿塞托有限公司 | Polymer composition comprising an alkaline additive, method and article comprising said polymer composition |
US11920260B2 (en) | 2014-12-11 | 2024-03-05 | Rhodia Acetow Gmbh | Polymer composition comprising basic additive, process and articles comprising said polymer composition |
WO2018033476A1 (en) * | 2016-08-17 | 2018-02-22 | Philip Morris Products S.A. | Aerosol-generating article having novel tobacco substrate |
US11399563B2 (en) | 2016-08-17 | 2022-08-02 | Philip Morris Products S.A. | Aerosol-generating article having novel tobacco substrate |
Also Published As
Publication number | Publication date |
---|---|
FI55604C (en) | 1979-09-10 |
ZA728844B (en) | 1973-10-31 |
BE794461A (en) | 1973-07-24 |
NL167845B (en) | 1981-09-16 |
NL167845C (en) | 1982-02-16 |
GB1400197A (en) | 1975-07-16 |
NL7301195A (en) | 1973-07-30 |
DK130764C (en) | 1975-09-15 |
AU463557B2 (en) | 1975-07-31 |
DK130764B (en) | 1975-04-14 |
CH573719A5 (en) | 1976-03-31 |
DE2263178B2 (en) | 1977-04-28 |
CA959369A (en) | 1974-12-17 |
DE2263178A1 (en) | 1973-08-02 |
FI55604B (en) | 1979-05-31 |
AU5014972A (en) | 1974-07-11 |
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