CA2567295A1 - Application of mesoporous molecular sieves as selective smoke filtration additives - Google Patents
Application of mesoporous molecular sieves as selective smoke filtration additives Download PDFInfo
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- CA2567295A1 CA2567295A1 CA002567295A CA2567295A CA2567295A1 CA 2567295 A1 CA2567295 A1 CA 2567295A1 CA 002567295 A CA002567295 A CA 002567295A CA 2567295 A CA2567295 A CA 2567295A CA 2567295 A1 CA2567295 A1 CA 2567295A1
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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
- A24D3/166—Silicic acid or silicates
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Abstract
A smoking article includes a filter element having MCM-41 as a mesoporous molecular sieve. Also, a smokable article includes a smokable material and a wrapping paper having MCM-41 as the mesoporous molecular sieve. The mesoporous molecular sieve may be used in combination with charcoal or impregnated with copper oxide to further enhance filtration.
Description
Application of Mesoporous Molecular Sieves as Selective Smoke Filtration Additives by Rodney D. Schluter and Lamar Perry CROSS-REFERENCE TO RELATED APPLICATIONS
This international patent application claims Paris Convention priority to and benefit from, currently pending, U.S. Patent Application serial number 10/860,775, filed on 03 June 2004.
STATEMENT REGARDING FEDERALLY SPONSORED RESEARCH OR
DEVELOPMENT
Not applicable.
REFERENCE TO A "SEQUENTIAL LISTING," A TABLE, OR A COMPUTER
PROGRAM LISTING APPENDIX SUBMITTED ON A COMPACT DISC
Not applicable.
BACKGROUND OF THE INVENTION
1. Field of the Invention The present invention relates to a smoking article having a filter element and/or smokable material containing a highly structured mesoporous molecular sieve, and more specifically, a smoking article having a filter element and/or smokable material containing a highly porous amorphous silica (hereinafter referred to as "MCM-41 "), as the highly structured mesoporous molecular sieve for filtering vapor phase constituents in mainstream smoke.
This international patent application claims Paris Convention priority to and benefit from, currently pending, U.S. Patent Application serial number 10/860,775, filed on 03 June 2004.
STATEMENT REGARDING FEDERALLY SPONSORED RESEARCH OR
DEVELOPMENT
Not applicable.
REFERENCE TO A "SEQUENTIAL LISTING," A TABLE, OR A COMPUTER
PROGRAM LISTING APPENDIX SUBMITTED ON A COMPACT DISC
Not applicable.
BACKGROUND OF THE INVENTION
1. Field of the Invention The present invention relates to a smoking article having a filter element and/or smokable material containing a highly structured mesoporous molecular sieve, and more specifically, a smoking article having a filter element and/or smokable material containing a highly porous amorphous silica (hereinafter referred to as "MCM-41 "), as the highly structured mesoporous molecular sieve for filtering vapor phase constituents in mainstream smoke.
2. Description of the Related Art Typical smoking articles, such as cigarettes, have a cylindrical filter element axially aligned with a cylindrical tobacco-filled rod. The filter element, and even the tobacco-filled rod, incorporate various materials that work to remove particular components from the mainstream smoke. Often, these materials are non-selective, thereby removing desirable components from the mainstream smoke and resulting in an undesirable taste.
Certain cigarettes have filter elements which incorporate materials such as carbon.
Exemplary cigarettes and filters are described in U.S. Patent Pub. No.
2003/0159703, to Yang, et al., and U.S. Patent Pub. No. 2003/0154993, to Paine, III et al.
Generally, surface area is inversely proportional to carbon particle size. If the particle size is too large, there may be insufficient surface area to accomplish the desired filtration. This factor must be taken into careful consideration when selecting a particular carbon particle size. Also, filter elements which incorporate carbon often yield a metallic flavor during smoking. Carbon is often impregnated with a flavorant in an attempt to camouflage the metallic flavor and may actually block the pores, an impediment to filtration, and finding a preferred flavorant loading percentage is difficult and inefficient. Furthermore, filter elements which incorporate carbon vary in proportion of micropores to mesopores, where the term "microporous"
generally refers to such materials having pore sizes of about 20A or less, while the term "mesoporous"
generally refers to such materials with pore sizes of about 20-500A. Uniform pore size distribution is more favorable. By having a more uniform pore size distribution, more of the porosity can be assured to be in the mesoporous range (2-50nm), which is more effective at filtering smoke than microporous materials. A variety of pore sizes is more likely to filter a variety of compounds, and filters for specific analytes are more desirable.
A smoking article with a filter element capable of filtering vapor phase components that is efficient to produce and does not yield a metallic flavor is desired.
Also, a filter element with a mesoporous molecular sieve that has uniform pore size is desired.
SUMMARY OF THE INVENTION
In view of known deficiencies associated with earlier smoking article filter elements, a smoking article with a mesoporous molecular sieve to filter vapor phase constituents from mainstream tobacco smoke is provided.
It has been found that a family of highly ordered mesoporous molecular sieves, manufactured by the Mobil Corporation and identified as M41 S, are useful in smoking article filter elements. M41 S materials are non-crystalline surfactant templated silica having a narrow pore size distribution. MCM-41 is a highly porous surfactant templated silica gel belonging to the M41 S family, and contains a highly organized hexagonal array of uniform pores with controllable diameters from about 15 A to about 100 A. The term "hexagonal"
encompasses materials that exhibit mathematically perfect hexagonal symmetry and materials with significant observable deviations from perfection. MCM refers to Mobil Composition of Matter or Mobil Crystalline Material, and was developed as a catalyst substrate by Mobil.
The surface chemistry of siliceous MCM-41 is comprised of silanol groups (SiOH), and may be synthesized using cetyltrimethylammonium chloride (CTAC1), H20, Na20, and SiOZ. The formed MCM-41 may be utilized as a mesoporous molecular sieve in smoking articles. MCM-41 has a highly condensed surface with less SiOH groups than silica, and its uniqueness is in the shape it adopts by forming around a template which is subsequently removed. The use of mesopores as an absorbent is taught by U.S. Patent No.
5,580,370, to Kuma, et al. Furthermore, MCM-41 has a large surface area, where the BET
surface area is approximately 1000 m2/g, and thus has a high sorption capacity. ("BET" refers to Brunaur, Emmett, and Teller, three scientists who optimized the theory for measuring surface areas.) MCM-41 is effective for reducing levels of alcohols, aldehydes, ketones, nitriles, and naphthalene.
It is an object of the present invention to provide a smoking article with a filter element having a mesoporous molecular sieve, MCM-41. A preferred smoking article is a cigarette with MCM-41 disposed within the filter element.
It is another object to provide a smokable material in a smokable rod of the smoking article having the mesoporous molecular sieve, MCM-41. A preferred smoking article is a cigarette and a preferred smokable material is tobacco. In this embodiment, MCM-41 is disposed within the smokable material in the rod.
It is yet another object to provide the filter element and the smokable material in the smokable rod of the smoking article both having the mesoporous molecular sieve, MCM-4 1.
In this embodiment, MCM-41 is disposed within the filter element and throughout the smokable material in the rod.
It is still yet a further object to provide either or both the filter element or the smokable material in the smokable rod of the smoking article having the mesoporous molecular sieve, MCM-41, in combination with charcoal, an ion-exchange resin, or both.
It is still yet another object to provide either or both the filter element or the smokable material in the smokable rod of the smoking article having an impregnated mesoporous molecular sieve, MCM-4 1. MCM-41 can be impregnated with copper oxide for greater HCN
and H2S reduction.
BRIEF DESCRIPTION OF THE DRAWINGS
The aspects and advantages of the present invention will be better understood when the detailed description of the preferred embodiment is taken in conjunction with the accompanying drawings, in which:
Certain cigarettes have filter elements which incorporate materials such as carbon.
Exemplary cigarettes and filters are described in U.S. Patent Pub. No.
2003/0159703, to Yang, et al., and U.S. Patent Pub. No. 2003/0154993, to Paine, III et al.
Generally, surface area is inversely proportional to carbon particle size. If the particle size is too large, there may be insufficient surface area to accomplish the desired filtration. This factor must be taken into careful consideration when selecting a particular carbon particle size. Also, filter elements which incorporate carbon often yield a metallic flavor during smoking. Carbon is often impregnated with a flavorant in an attempt to camouflage the metallic flavor and may actually block the pores, an impediment to filtration, and finding a preferred flavorant loading percentage is difficult and inefficient. Furthermore, filter elements which incorporate carbon vary in proportion of micropores to mesopores, where the term "microporous"
generally refers to such materials having pore sizes of about 20A or less, while the term "mesoporous"
generally refers to such materials with pore sizes of about 20-500A. Uniform pore size distribution is more favorable. By having a more uniform pore size distribution, more of the porosity can be assured to be in the mesoporous range (2-50nm), which is more effective at filtering smoke than microporous materials. A variety of pore sizes is more likely to filter a variety of compounds, and filters for specific analytes are more desirable.
A smoking article with a filter element capable of filtering vapor phase components that is efficient to produce and does not yield a metallic flavor is desired.
Also, a filter element with a mesoporous molecular sieve that has uniform pore size is desired.
SUMMARY OF THE INVENTION
In view of known deficiencies associated with earlier smoking article filter elements, a smoking article with a mesoporous molecular sieve to filter vapor phase constituents from mainstream tobacco smoke is provided.
It has been found that a family of highly ordered mesoporous molecular sieves, manufactured by the Mobil Corporation and identified as M41 S, are useful in smoking article filter elements. M41 S materials are non-crystalline surfactant templated silica having a narrow pore size distribution. MCM-41 is a highly porous surfactant templated silica gel belonging to the M41 S family, and contains a highly organized hexagonal array of uniform pores with controllable diameters from about 15 A to about 100 A. The term "hexagonal"
encompasses materials that exhibit mathematically perfect hexagonal symmetry and materials with significant observable deviations from perfection. MCM refers to Mobil Composition of Matter or Mobil Crystalline Material, and was developed as a catalyst substrate by Mobil.
The surface chemistry of siliceous MCM-41 is comprised of silanol groups (SiOH), and may be synthesized using cetyltrimethylammonium chloride (CTAC1), H20, Na20, and SiOZ. The formed MCM-41 may be utilized as a mesoporous molecular sieve in smoking articles. MCM-41 has a highly condensed surface with less SiOH groups than silica, and its uniqueness is in the shape it adopts by forming around a template which is subsequently removed. The use of mesopores as an absorbent is taught by U.S. Patent No.
5,580,370, to Kuma, et al. Furthermore, MCM-41 has a large surface area, where the BET
surface area is approximately 1000 m2/g, and thus has a high sorption capacity. ("BET" refers to Brunaur, Emmett, and Teller, three scientists who optimized the theory for measuring surface areas.) MCM-41 is effective for reducing levels of alcohols, aldehydes, ketones, nitriles, and naphthalene.
It is an object of the present invention to provide a smoking article with a filter element having a mesoporous molecular sieve, MCM-41. A preferred smoking article is a cigarette with MCM-41 disposed within the filter element.
It is another object to provide a smokable material in a smokable rod of the smoking article having the mesoporous molecular sieve, MCM-41. A preferred smoking article is a cigarette and a preferred smokable material is tobacco. In this embodiment, MCM-41 is disposed within the smokable material in the rod.
It is yet another object to provide the filter element and the smokable material in the smokable rod of the smoking article both having the mesoporous molecular sieve, MCM-4 1.
In this embodiment, MCM-41 is disposed within the filter element and throughout the smokable material in the rod.
It is still yet a further object to provide either or both the filter element or the smokable material in the smokable rod of the smoking article having the mesoporous molecular sieve, MCM-41, in combination with charcoal, an ion-exchange resin, or both.
It is still yet another object to provide either or both the filter element or the smokable material in the smokable rod of the smoking article having an impregnated mesoporous molecular sieve, MCM-4 1. MCM-41 can be impregnated with copper oxide for greater HCN
and H2S reduction.
BRIEF DESCRIPTION OF THE DRAWINGS
The aspects and advantages of the present invention will be better understood when the detailed description of the preferred embodiment is taken in conjunction with the accompanying drawings, in which:
FIG. 1 is a graph showing total particulate matter normalized percentage reductions of various vapor phase analytes when utilizing MCM-41 in a cigarette filter.
FIG. 2 is a graph showing total particulate matter normalized percentage reductions of mainstream smoke carbonyls.
FIG. 3 is a graph showing selected vapor phase analytes percentage reductions of MCM-41 and Sorbite.
FIG. 4 is a graph showing mainstream smoke carbonyl percentage reductions of MCM-41 and Sorbite.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
While this invention is susceptible of embodiments in many different forms, there are shown in the figures and will herein be described in detail, preferred embodiments of the invention with the understanding that the present disclosure is to be considered as an exemplification of the principles of the invention, and is not intended to limit the broad aspects of the invention to the embodiments illustrated.
The present invention provides for an article for smoking with a mesoporous molecular sieve, MCM-4 1, to filter vapor phase constituents from mainstream tobacco smoke. Vapor phase constituents to be filtered contact MCM-41 and are retained within the pores, thereby providing a separation of the undesirable constituents from the remainder of the vapor. MCM-41 is typically a black or white granular material with a density of =0.3g/cm3 and a BET surface area of =1000m2/g. Although pore wall thickness may vary, MCM-41 typically has a uniform pore diameter of ;zz:3.7nm, when cetyltrimethyl ammonium bromide is used.
The following examples are given for illustrative purposes only and are not to be deemed as limitative of the scope of the invention.
FIG. 2 is a graph showing total particulate matter normalized percentage reductions of mainstream smoke carbonyls.
FIG. 3 is a graph showing selected vapor phase analytes percentage reductions of MCM-41 and Sorbite.
FIG. 4 is a graph showing mainstream smoke carbonyl percentage reductions of MCM-41 and Sorbite.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
While this invention is susceptible of embodiments in many different forms, there are shown in the figures and will herein be described in detail, preferred embodiments of the invention with the understanding that the present disclosure is to be considered as an exemplification of the principles of the invention, and is not intended to limit the broad aspects of the invention to the embodiments illustrated.
The present invention provides for an article for smoking with a mesoporous molecular sieve, MCM-4 1, to filter vapor phase constituents from mainstream tobacco smoke. Vapor phase constituents to be filtered contact MCM-41 and are retained within the pores, thereby providing a separation of the undesirable constituents from the remainder of the vapor. MCM-41 is typically a black or white granular material with a density of =0.3g/cm3 and a BET surface area of =1000m2/g. Although pore wall thickness may vary, MCM-41 typically has a uniform pore diameter of ;zz:3.7nm, when cetyltrimethyl ammonium bromide is used.
The following examples are given for illustrative purposes only and are not to be deemed as limitative of the scope of the invention.
Example 1 To evaluate the adsorptive properties of MCM-41, MCM-41 was tested in hand-made cavity filters and compared to semolina (inert flour granules used to simulate a granule-filled cavity). Hand-made cavity filters can be made by first removing the cellulose acetate (CA) filter of a cigarette. Shortened segments of CA on the tobacco and mouth end of the filter create a cavity to hold the granular material.
The MCM-41 sample sets were prepared according to usual synthesis procedure, except for minor modifications. MCM-41 was developed by Exxon/Mobil, but sainple sets for experiment purposes were developed in the laboratory. Water, the surfactant cetyltrimethyl ammonium bromide (CTAB), and tetraethyl orthosilicate (TEOS) were mixed, in order, in a 250mL glass bottle until a cloudy white suspension was achieved. CTAB and TEOS were combined with a surfactant:silica mole ratio of 1:2. The solution's surfactant concentration, by total weight, equaled 25%. Concentrated sulfuric acid was added drop wise until the mixture changed to a clear liquid. The solution was stirred at approximately 400 rpm for .5 hours, and then placed under static autogenous conditions (121 C, 1 8psi) for 1 hour. The resulting gel was removed from the autoclave and allowed to cool before being washed thoroughly with deionized water. The washed material was heated at 570 C for six to eight hours in air, resulting in a porous material with a BET surface area of = 1300m2/g.
Sample sets of cigarettes containing 50mg of a granular additive in a hand-made cavity filter were prepared using either MCM-41 synthesized as described above or semolina.
Each sample set was pressure drop selected to decrease smoke delivery variances. Samples were conditioned (65% relative humidity and 75 C for 48 hours) and analyzed for total measured vapor phase (TMVP), mainstream smoke (MSS) HCN, and MSS carbonyl deliveries.
The MCM-41 sample sets were prepared according to usual synthesis procedure, except for minor modifications. MCM-41 was developed by Exxon/Mobil, but sainple sets for experiment purposes were developed in the laboratory. Water, the surfactant cetyltrimethyl ammonium bromide (CTAB), and tetraethyl orthosilicate (TEOS) were mixed, in order, in a 250mL glass bottle until a cloudy white suspension was achieved. CTAB and TEOS were combined with a surfactant:silica mole ratio of 1:2. The solution's surfactant concentration, by total weight, equaled 25%. Concentrated sulfuric acid was added drop wise until the mixture changed to a clear liquid. The solution was stirred at approximately 400 rpm for .5 hours, and then placed under static autogenous conditions (121 C, 1 8psi) for 1 hour. The resulting gel was removed from the autoclave and allowed to cool before being washed thoroughly with deionized water. The washed material was heated at 570 C for six to eight hours in air, resulting in a porous material with a BET surface area of = 1300m2/g.
Sample sets of cigarettes containing 50mg of a granular additive in a hand-made cavity filter were prepared using either MCM-41 synthesized as described above or semolina.
Each sample set was pressure drop selected to decrease smoke delivery variances. Samples were conditioned (65% relative humidity and 75 C for 48 hours) and analyzed for total measured vapor phase (TMVP), mainstream smoke (MSS) HCN, and MSS carbonyl deliveries.
Cigarettes with cavities containing 50mg of either semolina or MCM-41 were analyzed for TMVP smoke deliveries. TABLE A shows the results for selected vapor phase smoke compounds, comparing semolina with MCM-4 1:
TABLE A. Vapor Phase Smoke Analysis Data (Ng/cig) T Semolina (50 MCM-41 (50 Analyte mg/tip) mg/tip) H dro en sulfide 21.0 22.3 H dro en cyanide 76.4 68.1 Methanol 79.5 30.4 Acetaldehyde 647.0 536.1 Vinyl chloride 0.0 0.0 1,3-Butadiene 55.6 54.2 Acetonitrile 69.6 33.6 Propylene oxide 2.9 1.8 Acrolein 82.0 45.8 Furan 27.9 22.4 Pro ionaideh de 62.7 33.3 Acetone 228.5 91.1 Acrylonitrile 10.3 6.0 Carbon disulfide 3.8 4.0 Iso rene 396.4 371.5 Propionitrile 11.6 4.5 i-But raideh de 18.1 10.0 Methacrylonitrile 2.2 1.2 n-But raideh de 6.5 3.5 Methyl ethyl ketone 48.3 15.0 Crotonaldeh de 12.6 6.8 Benzene 35.1 33.3 Toluene 35.1 28.1 Styrene 3.0 1.3 Total TMVP 1936.1 1424.3 TPM m /ci 13.1 12.7 TMVP/TPM 147.8 112.1 (pg/mg) MCM-41 showed a greater reduction of analytes in the TMVP/TPM of 112.1 g/mg.
TMVP/TPM was higher with semolina (147.8 g/mg). FIG. 1 shows computed total particulate matter (TPM) normalized percentage reductions for various vapor phase constituents. These data suggest that the MCM-41 sample exhibited high filtration efficiencies for nitriles, ketones, and aldehydes when compared to the semolina control.
TABLE A. Vapor Phase Smoke Analysis Data (Ng/cig) T Semolina (50 MCM-41 (50 Analyte mg/tip) mg/tip) H dro en sulfide 21.0 22.3 H dro en cyanide 76.4 68.1 Methanol 79.5 30.4 Acetaldehyde 647.0 536.1 Vinyl chloride 0.0 0.0 1,3-Butadiene 55.6 54.2 Acetonitrile 69.6 33.6 Propylene oxide 2.9 1.8 Acrolein 82.0 45.8 Furan 27.9 22.4 Pro ionaideh de 62.7 33.3 Acetone 228.5 91.1 Acrylonitrile 10.3 6.0 Carbon disulfide 3.8 4.0 Iso rene 396.4 371.5 Propionitrile 11.6 4.5 i-But raideh de 18.1 10.0 Methacrylonitrile 2.2 1.2 n-But raideh de 6.5 3.5 Methyl ethyl ketone 48.3 15.0 Crotonaldeh de 12.6 6.8 Benzene 35.1 33.3 Toluene 35.1 28.1 Styrene 3.0 1.3 Total TMVP 1936.1 1424.3 TPM m /ci 13.1 12.7 TMVP/TPM 147.8 112.1 (pg/mg) MCM-41 showed a greater reduction of analytes in the TMVP/TPM of 112.1 g/mg.
TMVP/TPM was higher with semolina (147.8 g/mg). FIG. 1 shows computed total particulate matter (TPM) normalized percentage reductions for various vapor phase constituents. These data suggest that the MCM-41 sample exhibited high filtration efficiencies for nitriles, ketones, and aldehydes when compared to the semolina control.
Large percentage reductions were shown for the analytes Propionitrile (58%), Methanol (59%), Methyl Ethyl Ketone (66%), and Propionaldehyde (43%). Overall, TMVP
deliveries were reduced by 24% when utilizing MCM-41.
Mainstream smoke (MSS) carbonyl deliveries for semolina and MCM-41 are compared in TABLE B:
TABLE B. MSS Carbonyl Deliveries ( g/cig) Analyte Semolina MCM-41 (50 mg/tip) (50 mg/tip) Acetaldeh de 701.7 444.8 Acetone 276.4 72.4 Acrolein 115.1 46.2 Butanone 84.6 17.9 But raideh de 45.8 14.1 Crotonaldeh de 28.0 10.9 Formaldehyde 55.7 34.4 Pro ionaideh de 58.2 24.5 Total 1366.0 664.0 TPM m /ci 13.1 12.7 Total/TPM 104.3 52.3 (pg/mg) MCM-41 yielded less carbonyl in the mainstream smoke delivery than did semolina:
52.3 g/mg compared with 104.3 g/mg, respectively. TPM normalized percentage reduction for mainstream smoke carbonyls is shown in FIG. 2. The data indicates that the sample displayed an increased affinity for MSS carbonyls versus the semolina control. The MCM-41 sample reduced mainstream smoke carbonyl deliveries by a total of 49%
compared to the semolina sample. MCM-41 reductions above 50% were calculated, versus the control, for the analytes acrolein, acetone, butanone, and butyraldehyde. Measured formaldehyde deliveries, when using MCM-41, showed a 34% reduction versus semolina.
deliveries were reduced by 24% when utilizing MCM-41.
Mainstream smoke (MSS) carbonyl deliveries for semolina and MCM-41 are compared in TABLE B:
TABLE B. MSS Carbonyl Deliveries ( g/cig) Analyte Semolina MCM-41 (50 mg/tip) (50 mg/tip) Acetaldeh de 701.7 444.8 Acetone 276.4 72.4 Acrolein 115.1 46.2 Butanone 84.6 17.9 But raideh de 45.8 14.1 Crotonaldeh de 28.0 10.9 Formaldehyde 55.7 34.4 Pro ionaideh de 58.2 24.5 Total 1366.0 664.0 TPM m /ci 13.1 12.7 Total/TPM 104.3 52.3 (pg/mg) MCM-41 yielded less carbonyl in the mainstream smoke delivery than did semolina:
52.3 g/mg compared with 104.3 g/mg, respectively. TPM normalized percentage reduction for mainstream smoke carbonyls is shown in FIG. 2. The data indicates that the sample displayed an increased affinity for MSS carbonyls versus the semolina control. The MCM-41 sample reduced mainstream smoke carbonyl deliveries by a total of 49%
compared to the semolina sample. MCM-41 reductions above 50% were calculated, versus the control, for the analytes acrolein, acetone, butanone, and butyraldehyde. Measured formaldehyde deliveries, when using MCM-41, showed a 34% reduction versus semolina.
TABLE C shows a summary of mean polycyclic aromatic hydrocarbon (PAH) deliveries in particulate phase smoke:
TABLE C. The Mean Levels of PAHs for the Cigarette Sam ples Semolina MCM-41 Naphthalene 365.6 284.5 Fluorene 127.2 134.9 Phenanthrene 103.4 113.7 Anthracene 40.3 43.6 Fluoranthene 58.7 61.5 Pyrene 38.4 39.1 Benzofluorene 30.3 32.0 Benzanthracene 16.8 17.2 Chrysene 17.2 18.2 Benzofluoranthene 7.0 7.3 Benzo e rene 3.7 3.8 Benzo[a]pyrene (BAP) 5.8 6.1 Pe lene 0.6 0.7 Dibenzanthracene 0.2 0.2 Benzo e lene 1.1 1.2 Total PAH (ng/cig) 816.4 763.9 TPM m /ci 11.3 11.8 Puff Number 6.9 6.8 PAH per TPM
n /m 72.0 64.6 BAP per TPM
n /m 0.52 0.51 When comparing the semolina with MCM-41, total particulate matter (TPM) normalized results suggest naphthalene deliveries were reduced by =29%. This effect may be due to the fact that naphthalene is the smallest and most volatile of the PAHs measured, demonstrating MCM-41's high affinity for small and volatile compounds. All other PAH
compounds analyzed failed to show an appreciable affinity for the MCM-41 sample versus the control.
To summarize, the MCM-41 samples were found to be an effective adsorbent for select constituents found in mainstream smoke. Significant reductions were observed for nitrile, aldehyde, and ketone deliveries. In addition, PAH deliveries indicate reduction for naphthalene. MCM-41 has an affinity for molecules that form strong intermolecular bonds, and therefore, no reductions were observed for the analytes 1,3-butadiene, isoprene, furan, and benzene. The MCM-41 samples exhibited high filtration efficiencies for nitriles, aldehydes, and ketones when compared to the semolina control. In addition, MCM-displayed selectivity for naphthalene.
Example 2 To evaluate the filtration efficiency of MCM-41, MCM-41 and Sorbite, a coal-based activated carbon derived from semi-anthracite coal, available from Calgon Carbons, were placed in hand-made cavity filtered cigarettes, the properties of which are explained above, and the filtration efficiencies of both were compared. Semolina was utilized as a control.
The highly porous nature of MCM-41 invited the comparison to activated carbons, such as Sorbite. The MCM-41 samples were prepared according to the above-stated method. Sorbite was used without modification.
Three sample sets were prepared with hand-made cavity filtered cigarettes.
TABLE D
lists the filter additives and loadings for each sample:
TABLE D. Loadin Amounts for Filter Components Filter Components Loading (mg) MCM-41/Semolina 50/50 Sorbite/Semolina 50/50 Semolina Control 100 The samples were pressure drop selected to diminish variances in aerosol deliveries. After conditioning, the samples were analyzed for total measured vapor phase (TMVP), polycyclic aromatic hydrocarbon (PAH), and mainstream smoke carbonyl (MSS carbonyl) deliveries.
All three samples were analyzed for TMVP. TABLE E lists vapor phase deliveries for each sample:
TABLE E. Vapor Phase Smoke Analysis Data ( g/cig) Semolina Sorbite/Semolina MCM-41/Semolina 1,3-Butadiene 69.8 69.8 69.7 Acetaldehyde 627.1 636.2 541.9 Acetone 294.7 216.5 120.9 Acetonitrile 84.2 69.6 45.2 Acrolein 75.9 50.6 43.4 Acrylonitrile 13.3 10.0 8.7 Benzene 58.9 31.6 41.2 Carbon Disulfide 4.1 3.9 3.9 Crotonaldehyde 21.6 6.3 8.3 Furan 41.4 39.1 38.9 H dro en Cyanide 78.0 73.3 70.7 H dro en Sulfide 20.0 15.1 19.9 Iso rene 551.4 426.2 473.7 Methacrylonitrile 2.5 1.5 1.3 Methanol 80.9 72.3 34.9 Methyl Ethyl Ketone 68.4 32.0 17.1 Pro ionaldeh de 58.2 45.7 39.4 Propionitrile 13.6 8.1 5.2 Propylene Oxide 3.8 3.8 3.0 Styrene 5.8 2.5 3.6 Toluene 62.7 23.8 35.7 Vinyl Chloride BQL BQL BQL
I-Bu raldeh de 28.7 21.0 18.2 N-Butyraldehyde 8.7 5.3 4.4 TMVP 2273.1 1863.7 1648.7 TPM 12.6 12.8 12.5 TMVP/TPM 180.4 145.6 131.9 A direct comparison of the vapor phase data for MCM-41 and Sorbite reveals that, while activated carbons are a good general adsorbent for a broad range of analytes, MCM-41 is selective for the more polar analytes such as nitriles, aldehydes, ketones, and alcohols. This affinity for polar molecules can be explained by their strong intermolecular bonding with pendant hydroxide groups on the surface of the silica, and FIG. 3 displays the selectivity of MCM-41.
All three samples were also analyzed for mainstream smoke carbonyls with the deliveries listed in TABLE F:
TABLE F. MSS Carbonyl Deliveries (Ng/cig) Semolina Sorbite/Sem* MCM41/Sem*
Acetaldeh de 641.5 561.2 539.8 Acetone 256.7 164.2 104.9 Acrolein 106.7 64.4 67.4 Butanone 74.7 33.0 24.8 But raldeh de 40.8 19.8 18.5 Crotonaldeh de 27.2 16.7 11.6 Formaldehyde 51.8 43.6 40.1 Pro ionaideh de 53.9 33.6 35.0 Total Carbon Is 1253.3 936.6 842.0 Total Carbon Is/TPM 99.5 73.2 67.4 *Sem= Semolina TABLE F shows mainstream smoke carbonyl deliveries comparing semolina, Sorbite/semolina, and MCM-4 1 /semolina. MCM-41 delivered 842.0 g/cigarette total carbonyls, while Sorbite delivered more carbonyls: 936.6 g/cigarette. FIG. 4 shows normalized percentage reductions for mainstream smoke carbonyls of MCM-41 and Sorbite.
These results were consistent with the results of the vapor phase analyses.
Reductions observed for the surfactant templated silica were (at a minimum) comparable to reductions for the Sorbite samples. A few analytes, such as acetone and crotonaldehyde, had greater reductions.
Deliveries of polycyclic aromatic hydrocarbons (PAHs) were measured because of known reductions in naphthalene for samples containing MCM-4 1. TABLE G shows a complete list of PAH test results:
TABLE G. Polycyclic Aromatic Hydrocarbons (PAH) Analysis Data (pg/cig) PAHS - FTC Semolina Sorbite/Sem MCM41/Sem Anthrecene 40.8 41.4 42.1 Benzanthracene 16.4 16.9 17.2 Benzo a rene 6.2 6.2 6.2 Benzo e rene 4.4 4.6 4.5 Benzofluoranthene 7.4 7.5 7.4 Benzofluorene 28.5 28.7 30.6 Benzo e lene 1.2 1.2 1.2 Chrysene 18.8 19.0 19.4 Dibenzanthracene 0.2 0.2 0.2 Fluoranthene 47.0 45.8 49.4 Fluorene 130.0 126.0 131.5 Naphthalene 453.0 198.0 271.0 Pe iene 0.6 0.6 0.6 Phenanthrene 111.0 110.5 111.0 Pyrene 39.5 39.0 39.9 PAHS TPM 13.3 12.7 13.2 Total PAH 904.9 645.3 732.0 Total PAH / TPM 68.3 50.7 55.4 Total particulate matter (TPM) normalized reductions of naphthalene versus a semolina control for MCM-41 was =40%, and for Sorbite was =54%. No other reductions in PAHs were observed. Although naphthalene is the smallest and most volatile of the PAH analytes measured, reductions in naphthalene are presumably due to its volatility and not its size. The pore diameter of MCM-41 is large relative to anthracene, the next smallest analyte measured, in which no reductions were observed. These numbers reflect the capacity of Sorbite to adsorb non-polar molecules.
To summarize, the MCM-41 sample was found to be more selective for polar smoke constituents and outperformed the Sorbite for the removal of nitriles, ketones, alcohols, and aldehydes. The Sorbite sample was more selective for non-polar smoke constituents such as benzene, toluene, styrene, isoprene, and naphthalene. MCM-41 can compliment Sorbite and other additives, such as an ion-exchange resin, as a co-additive.
A sample of MCM-41 was prepared using the process as described in EXAMPLE 1.
Additionally, copper nitrate was introduced into the MCM-41 reaction solution with a concentration of 3% by weight. The resulting gel was calcined at 400 C, forming a copper oxide impregnated MCM-41 having the same high surface area and vapor phase capacity as pure MCM-41, but with the added ability to reduce hydrogen cyanide and hydrogen sulfide.
Compared to the semolina control as previously described, copper oxide impregnated MCM-41 showed a 56% reduction in HCN ad a 35% reduction in H2S.
The foregoing detailed description is given primarily for clearness of understanding and no unnecessary limitations are to be understood therefrom, for modifications will become obvious to those skilled in the art upon reading this disclosure, and may be made without departing from the spirit of the invention and scope of the appended claims.
TABLE C. The Mean Levels of PAHs for the Cigarette Sam ples Semolina MCM-41 Naphthalene 365.6 284.5 Fluorene 127.2 134.9 Phenanthrene 103.4 113.7 Anthracene 40.3 43.6 Fluoranthene 58.7 61.5 Pyrene 38.4 39.1 Benzofluorene 30.3 32.0 Benzanthracene 16.8 17.2 Chrysene 17.2 18.2 Benzofluoranthene 7.0 7.3 Benzo e rene 3.7 3.8 Benzo[a]pyrene (BAP) 5.8 6.1 Pe lene 0.6 0.7 Dibenzanthracene 0.2 0.2 Benzo e lene 1.1 1.2 Total PAH (ng/cig) 816.4 763.9 TPM m /ci 11.3 11.8 Puff Number 6.9 6.8 PAH per TPM
n /m 72.0 64.6 BAP per TPM
n /m 0.52 0.51 When comparing the semolina with MCM-41, total particulate matter (TPM) normalized results suggest naphthalene deliveries were reduced by =29%. This effect may be due to the fact that naphthalene is the smallest and most volatile of the PAHs measured, demonstrating MCM-41's high affinity for small and volatile compounds. All other PAH
compounds analyzed failed to show an appreciable affinity for the MCM-41 sample versus the control.
To summarize, the MCM-41 samples were found to be an effective adsorbent for select constituents found in mainstream smoke. Significant reductions were observed for nitrile, aldehyde, and ketone deliveries. In addition, PAH deliveries indicate reduction for naphthalene. MCM-41 has an affinity for molecules that form strong intermolecular bonds, and therefore, no reductions were observed for the analytes 1,3-butadiene, isoprene, furan, and benzene. The MCM-41 samples exhibited high filtration efficiencies for nitriles, aldehydes, and ketones when compared to the semolina control. In addition, MCM-displayed selectivity for naphthalene.
Example 2 To evaluate the filtration efficiency of MCM-41, MCM-41 and Sorbite, a coal-based activated carbon derived from semi-anthracite coal, available from Calgon Carbons, were placed in hand-made cavity filtered cigarettes, the properties of which are explained above, and the filtration efficiencies of both were compared. Semolina was utilized as a control.
The highly porous nature of MCM-41 invited the comparison to activated carbons, such as Sorbite. The MCM-41 samples were prepared according to the above-stated method. Sorbite was used without modification.
Three sample sets were prepared with hand-made cavity filtered cigarettes.
TABLE D
lists the filter additives and loadings for each sample:
TABLE D. Loadin Amounts for Filter Components Filter Components Loading (mg) MCM-41/Semolina 50/50 Sorbite/Semolina 50/50 Semolina Control 100 The samples were pressure drop selected to diminish variances in aerosol deliveries. After conditioning, the samples were analyzed for total measured vapor phase (TMVP), polycyclic aromatic hydrocarbon (PAH), and mainstream smoke carbonyl (MSS carbonyl) deliveries.
All three samples were analyzed for TMVP. TABLE E lists vapor phase deliveries for each sample:
TABLE E. Vapor Phase Smoke Analysis Data ( g/cig) Semolina Sorbite/Semolina MCM-41/Semolina 1,3-Butadiene 69.8 69.8 69.7 Acetaldehyde 627.1 636.2 541.9 Acetone 294.7 216.5 120.9 Acetonitrile 84.2 69.6 45.2 Acrolein 75.9 50.6 43.4 Acrylonitrile 13.3 10.0 8.7 Benzene 58.9 31.6 41.2 Carbon Disulfide 4.1 3.9 3.9 Crotonaldehyde 21.6 6.3 8.3 Furan 41.4 39.1 38.9 H dro en Cyanide 78.0 73.3 70.7 H dro en Sulfide 20.0 15.1 19.9 Iso rene 551.4 426.2 473.7 Methacrylonitrile 2.5 1.5 1.3 Methanol 80.9 72.3 34.9 Methyl Ethyl Ketone 68.4 32.0 17.1 Pro ionaldeh de 58.2 45.7 39.4 Propionitrile 13.6 8.1 5.2 Propylene Oxide 3.8 3.8 3.0 Styrene 5.8 2.5 3.6 Toluene 62.7 23.8 35.7 Vinyl Chloride BQL BQL BQL
I-Bu raldeh de 28.7 21.0 18.2 N-Butyraldehyde 8.7 5.3 4.4 TMVP 2273.1 1863.7 1648.7 TPM 12.6 12.8 12.5 TMVP/TPM 180.4 145.6 131.9 A direct comparison of the vapor phase data for MCM-41 and Sorbite reveals that, while activated carbons are a good general adsorbent for a broad range of analytes, MCM-41 is selective for the more polar analytes such as nitriles, aldehydes, ketones, and alcohols. This affinity for polar molecules can be explained by their strong intermolecular bonding with pendant hydroxide groups on the surface of the silica, and FIG. 3 displays the selectivity of MCM-41.
All three samples were also analyzed for mainstream smoke carbonyls with the deliveries listed in TABLE F:
TABLE F. MSS Carbonyl Deliveries (Ng/cig) Semolina Sorbite/Sem* MCM41/Sem*
Acetaldeh de 641.5 561.2 539.8 Acetone 256.7 164.2 104.9 Acrolein 106.7 64.4 67.4 Butanone 74.7 33.0 24.8 But raldeh de 40.8 19.8 18.5 Crotonaldeh de 27.2 16.7 11.6 Formaldehyde 51.8 43.6 40.1 Pro ionaideh de 53.9 33.6 35.0 Total Carbon Is 1253.3 936.6 842.0 Total Carbon Is/TPM 99.5 73.2 67.4 *Sem= Semolina TABLE F shows mainstream smoke carbonyl deliveries comparing semolina, Sorbite/semolina, and MCM-4 1 /semolina. MCM-41 delivered 842.0 g/cigarette total carbonyls, while Sorbite delivered more carbonyls: 936.6 g/cigarette. FIG. 4 shows normalized percentage reductions for mainstream smoke carbonyls of MCM-41 and Sorbite.
These results were consistent with the results of the vapor phase analyses.
Reductions observed for the surfactant templated silica were (at a minimum) comparable to reductions for the Sorbite samples. A few analytes, such as acetone and crotonaldehyde, had greater reductions.
Deliveries of polycyclic aromatic hydrocarbons (PAHs) were measured because of known reductions in naphthalene for samples containing MCM-4 1. TABLE G shows a complete list of PAH test results:
TABLE G. Polycyclic Aromatic Hydrocarbons (PAH) Analysis Data (pg/cig) PAHS - FTC Semolina Sorbite/Sem MCM41/Sem Anthrecene 40.8 41.4 42.1 Benzanthracene 16.4 16.9 17.2 Benzo a rene 6.2 6.2 6.2 Benzo e rene 4.4 4.6 4.5 Benzofluoranthene 7.4 7.5 7.4 Benzofluorene 28.5 28.7 30.6 Benzo e lene 1.2 1.2 1.2 Chrysene 18.8 19.0 19.4 Dibenzanthracene 0.2 0.2 0.2 Fluoranthene 47.0 45.8 49.4 Fluorene 130.0 126.0 131.5 Naphthalene 453.0 198.0 271.0 Pe iene 0.6 0.6 0.6 Phenanthrene 111.0 110.5 111.0 Pyrene 39.5 39.0 39.9 PAHS TPM 13.3 12.7 13.2 Total PAH 904.9 645.3 732.0 Total PAH / TPM 68.3 50.7 55.4 Total particulate matter (TPM) normalized reductions of naphthalene versus a semolina control for MCM-41 was =40%, and for Sorbite was =54%. No other reductions in PAHs were observed. Although naphthalene is the smallest and most volatile of the PAH analytes measured, reductions in naphthalene are presumably due to its volatility and not its size. The pore diameter of MCM-41 is large relative to anthracene, the next smallest analyte measured, in which no reductions were observed. These numbers reflect the capacity of Sorbite to adsorb non-polar molecules.
To summarize, the MCM-41 sample was found to be more selective for polar smoke constituents and outperformed the Sorbite for the removal of nitriles, ketones, alcohols, and aldehydes. The Sorbite sample was more selective for non-polar smoke constituents such as benzene, toluene, styrene, isoprene, and naphthalene. MCM-41 can compliment Sorbite and other additives, such as an ion-exchange resin, as a co-additive.
A sample of MCM-41 was prepared using the process as described in EXAMPLE 1.
Additionally, copper nitrate was introduced into the MCM-41 reaction solution with a concentration of 3% by weight. The resulting gel was calcined at 400 C, forming a copper oxide impregnated MCM-41 having the same high surface area and vapor phase capacity as pure MCM-41, but with the added ability to reduce hydrogen cyanide and hydrogen sulfide.
Compared to the semolina control as previously described, copper oxide impregnated MCM-41 showed a 56% reduction in HCN ad a 35% reduction in H2S.
The foregoing detailed description is given primarily for clearness of understanding and no unnecessary limitations are to be understood therefrom, for modifications will become obvious to those skilled in the art upon reading this disclosure, and may be made without departing from the spirit of the invention and scope of the appended claims.
Claims (54)
1. A smoking article, comprising:
a smokable material circumscribed with a wrapping material to form a smokable rod; and, an axially aligned filter element, wherein said filter element includes a mesoporous molecular sieve.
a smokable material circumscribed with a wrapping material to form a smokable rod; and, an axially aligned filter element, wherein said filter element includes a mesoporous molecular sieve.
2. The article of claim 1, wherein said mesoporous molecular sieve is disposed within said filter element.
3. The article of claim 1, wherein said filter element includes a plurality of filter cavities, wherein one or more of said filter cavities includes a mesoporous molecular sieve.
4. The article of claim 1, wherein said mesoporous molecular sieve is MCM-41.
5. The article of claim 1, wherein said mesoporous molecular sieve is a surfactant templated silica gel having an organized hexagonal array of uniform pores.
6. The article of claim 5, wherein said uniform pores have diameters of from about 15A
to about 100A.
to about 100A.
7. A smoking article, comprising:
a smokable material circumscribed with a wrapping material to form a smokable rod; and, an axially aligned filter element, wherein said smokable material includes a mesoporous molecular sieve, said mesoporous molecular sieve being disposed within said smokable rod.
a smokable material circumscribed with a wrapping material to form a smokable rod; and, an axially aligned filter element, wherein said smokable material includes a mesoporous molecular sieve, said mesoporous molecular sieve being disposed within said smokable rod.
8. The article of claim 7, wherein said wrapping material is coated with said mesoporous molecular sieve.
9. The article of claim 7, wherein said mesoporous molecular sieve is MCM-41.
10. The article of claim 7, wherein said mesoporous molecular sieve is a surfactant templated silica gel having an organized hexagonal array of uniform pores.
11. The article of claim 10, wherein said uniform pores have diameters of from about 15A
to about 100A.
to about 100A.
12. A smoking article, comprising:
a smokable material circumscribed with a wrapping material to form a smokable rod; and, an axially aligned filter element, wherein said smokable material, said wrapping material, and said filter element include a mesoporous molecular sieve, said mesoporous molecular sieve being disposed within said smokable material and said filter element and coated on said wrapping material.
a smokable material circumscribed with a wrapping material to form a smokable rod; and, an axially aligned filter element, wherein said smokable material, said wrapping material, and said filter element include a mesoporous molecular sieve, said mesoporous molecular sieve being disposed within said smokable material and said filter element and coated on said wrapping material.
13. The article of claim 12, wherein said mesoporous molecular sieve is MCM-41.
14. The article of claim 12, wherein said mesoporous molecular sieve is a surfactant templated silica gel having an organized hexagonal array of uniform pores
15. The article of claim 14, wherein said uniform pores have diameters of from about 15A
to about 100A.
to about 100A.
16. A cigarette, comprising:
a tobacco rod with a filter element attached thereto; and a mesoporous molecular sieve.
a tobacco rod with a filter element attached thereto; and a mesoporous molecular sieve.
17. The cigarette of claim 16, wherein said mesoporous molecular sieve is disposed within said filter element.
18. The cigarette of claim 16, wherein said filter element includes a plurality of filter cavities.
19. The cigarette of claim 18, wherein one or more of said filter cavities includes said mesoporous molecular sieve.
20. The cigarette of claim 16, wherein said filter element is attached in axial alignment with a tobacco-filled smokable rod, said smokable rod including said mesoporous molecular sieve disposed therein.
21. The cigarette of claim 20, wherein said filter element and said smokable rod are circumscribed with a wrapping paper, said wrapping paper coated with said mesoporous molecular sieve.
22. The cigarette of claim 16, wherein said mesoporous molecular sieve is MCM-41.
23. The cigarette of claim 16, wherein said mesoporous molecular sieve is a surfactant templated silica gel having an organized hexagonal array of uniform pores.
24. The cigarette of claim 23, wherein said uniform pores have diameters from about 15A
to about 100A.
to about 100A.
25. A smoking article, comprising:
a smokable material circumscribed with a wrapping material to form a smokable rod; and, an axially aligned filter element, wherein said smoking article includes a mesoporous molecular sieve and a plurality of additives.
a smokable material circumscribed with a wrapping material to form a smokable rod; and, an axially aligned filter element, wherein said smoking article includes a mesoporous molecular sieve and a plurality of additives.
26. The article of claim 25, wherein said mesoporous molecular sieve and said additives are disposed within said smokable material.
27. The article of claim 25, wherein said mesoporous molecular sieve and said additives are disposed within said filter element.
28. The article of claim 25, wherein said mesoporous molecular sieve and said additives are disposed within said smokable material and said filter element.
29. The article of claim 25, wherein said filter element includes a plurality of filter cavities, and wherein one or more of said filter cavities includes said mesoporous molecular sieve and said additives.
30. The article of claim 25, wherein said mesoporous molecular sieve is MCM-41.
31. The article of claim 25, wherein said mesoporous molecular sieve is a surfactant templated silica gel having an organized array of uniform pores.
32. The article of claim 31, wherein said uniform pores have diameters from about 15A to about 100A.
33. The article of claim 25, wherein one of said additives is an activated carbon.
34. The article of claim 33, wherein said activated carbon is a Sorbite.
35. The article of claim 25, wherein one of said additives is an ion-exchange resin.
36. A smoking article, comprising:
a smokable material circumscribed with a wrapping material to form a smokable rod; and, an axially aligned filter element, wherein said smoking article includes a mesoporous molecular sieve impregnated with copper oxide.
a smokable material circumscribed with a wrapping material to form a smokable rod; and, an axially aligned filter element, wherein said smoking article includes a mesoporous molecular sieve impregnated with copper oxide.
37. The article of claim 36, wherein said mesoporous molecular sieve impregnated with copper oxide is disposed within said smokable material.
38. The article of claim 36, wherein said filter element includes said mesoporous molecular sieve impregnated with copper oxide disposed therein.
39. The article of claim 36, wherein said filter element is comprised of a plurality of filter cavities, and wherein one or more of said filter cavities includes said mesoporous molecular sieve impregnated with copper oxide.
40. The article of claim 36, wherein said mesoporous molecular sieve impregnated with copper oxide is disposed within said smokable material and said filter element.
41. The article of claim 36, wherein said mesoporous molecular sieve is MCM-41.
42. The article of claim 36, wherein said mesoporous molecular sieve is a surfactant templated silica gel having an organized array of uniform pores.
43. The article of claim 42, wherein said uniform pores have diameters from about 15A to about 100A.
44. A filter for a smoking article, comprising:
a filter element with a mesoporous molecular sieve; and a plurality of additives disposed within said filter element.
a filter element with a mesoporous molecular sieve; and a plurality of additives disposed within said filter element.
45. The filter of claim 44, wherein said mesoporous molecular sieve and said additives are disposed within said filter element.
46. The filter of claim of 44, including a plurality of filter cavities.
47. The filter of claim 46, wherein at least one of said filter cavities includes a mesoporous molecular sieve and at least one of said filter cavities includes said additives.
48. The filter of claim 44, wherein said mesoporous molecular sieve is MCM-41.
49. The filter of claim 44, wherein said mesoporous molecular sieve is a surfactant templated silica gel having an organized array of uniform pores.
50. The filter of claim 49, wherein said uniform pores have diameters from about 15A to about 100A
51. The filter of claim 44, wherein one of said additives is an activated carbon.
52. The filter of claim 51, wherein said activated carbon is a Sorbite.
53. The filter of claim 44, wherein one of said additives is an ion-exchange resin.
54. The filter of claim 44, wherein said mesoporous molecular sieve is impregnated with copper oxide.
Applications Claiming Priority (3)
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US10/860,775 | 2004-06-03 | ||
US10/860,775 US20050268925A1 (en) | 2004-06-03 | 2004-06-03 | Application of mesoporous molecular sieves as selective smoke filtration additives |
PCT/US2005/015022 WO2005120261A1 (en) | 2004-06-03 | 2005-04-29 | Application of mesoporous molecular sieves as selective smoke filtration additives |
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US8434498B2 (en) | 2009-08-11 | 2013-05-07 | R. J. Reynolds Tobacco Company | Degradable filter element |
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CN101934234B (en) * | 2010-09-13 | 2012-07-04 | 中南大学 | Mesoporous molecular sieve catalyst for catalytic cracking of waste plastics as well as preparation method and application thereof |
US8973588B2 (en) | 2011-07-29 | 2015-03-10 | R.J. Reynolds Tobacco Company | Plasticizer composition for degradable polyester filter tow |
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US20130167851A1 (en) | 2011-12-28 | 2013-07-04 | Balager Ademe | Method of filter assembly for smoking article |
US20160073686A1 (en) | 2014-09-12 | 2016-03-17 | R.J. Reynolds Tobacco Company | Tobacco-derived filter element |
US10226066B2 (en) | 2016-03-07 | 2019-03-12 | R.J. Reynolds Tobacco Company | Rosemary in a tobacco blend |
CN106858717A (en) * | 2017-04-10 | 2017-06-20 | 滁州卷烟材料厂 | The filter tip of carbonyls in a kind of selectivity reducing cigarette fume |
CN113576027A (en) * | 2021-08-25 | 2021-11-02 | 上海烟草集团有限责任公司 | Composite filter stick for reducing propionaldehyde in cigarette smoke and cigarette |
CN113558290A (en) * | 2021-08-26 | 2021-10-29 | 上海烟草集团有限责任公司 | Method for reducing acetone in cigarette smoke |
CN114669272A (en) * | 2022-02-24 | 2022-06-28 | 昆明理工大学 | Adsorbent for synergistically removing dust, hydrogen fluoride and hydrogen chloride in copper smelting flue gas and preparation method thereof |
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- 2005-04-29 CN CNA2005800182850A patent/CN101010013A/en active Pending
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- 2005-05-24 PE PE2005000571A patent/PE20060071A1/en not_active Application Discontinuation
- 2005-05-27 UY UY28928A patent/UY28928A1/en not_active Application Discontinuation
- 2005-06-01 GT GT200500131A patent/GT200500131A/en unknown
- 2005-06-01 AR ARP050102248A patent/AR050414A1/en unknown
- 2005-06-02 SV SV2005002133A patent/SV2005002133A/en not_active Application Discontinuation
- 2005-06-02 TW TW094118086A patent/TW200614926A/en unknown
- 2005-06-03 PA PA20058635701A patent/PA8635701A1/en unknown
-
2006
- 2006-12-01 ZA ZA200610096A patent/ZA200610096B/en unknown
Also Published As
Publication number | Publication date |
---|---|
BRPI0511750A (en) | 2008-01-02 |
SV2005002133A (en) | 2011-03-22 |
PA8635701A1 (en) | 2006-10-13 |
RU2006146202A (en) | 2008-07-20 |
RU2337596C1 (en) | 2008-11-10 |
CN101010013A (en) | 2007-08-01 |
GT200500131A (en) | 2006-01-10 |
TW200614926A (en) | 2006-05-16 |
EP1750530A1 (en) | 2007-02-14 |
PE20060071A1 (en) | 2006-02-12 |
UY28928A1 (en) | 2006-01-31 |
ZA200610096B (en) | 2008-07-30 |
WO2005120261A1 (en) | 2005-12-22 |
US20050268925A1 (en) | 2005-12-08 |
AR050414A1 (en) | 2006-10-25 |
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