US3410282A - Filter medium for removing hydrogen cyanide from tobacco smoke - Google Patents
Filter medium for removing hydrogen cyanide from tobacco smoke Download PDFInfo
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- US3410282A US3410282A US622470A US62247067A US3410282A US 3410282 A US3410282 A US 3410282A US 622470 A US622470 A US 622470A US 62247067 A US62247067 A US 62247067A US 3410282 A US3410282 A US 3410282A
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- filter
- tobacco smoke
- smoke
- hydrogen cyanide
- filters
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- 239000000779 smoke Substances 0.000 title description 55
- LELOWRISYMNNSU-UHFFFAOYSA-N hydrogen cyanide Chemical compound N#C LELOWRISYMNNSU-UHFFFAOYSA-N 0.000 title description 39
- 241000208125 Nicotiana Species 0.000 title description 38
- 235000002637 Nicotiana tabacum Nutrition 0.000 title description 38
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 20
- 229920002301 cellulose acetate Polymers 0.000 description 20
- 235000019504 cigarettes Nutrition 0.000 description 19
- 150000003839 salts Chemical class 0.000 description 19
- -1 amine salt Chemical group 0.000 description 14
- 239000000654 additive Substances 0.000 description 10
- 229910052799 carbon Inorganic materials 0.000 description 10
- 239000000243 solution Substances 0.000 description 9
- 239000002253 acid Substances 0.000 description 8
- 150000001412 amines Chemical class 0.000 description 8
- 239000000463 material Substances 0.000 description 8
- 239000007787 solid Substances 0.000 description 8
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 6
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 6
- 150000001734 carboxylic acid salts Chemical class 0.000 description 6
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 6
- 239000013618 particulate matter Substances 0.000 description 6
- URAYPUMNDPQOKB-UHFFFAOYSA-N triacetin Chemical compound CC(=O)OCC(OC(C)=O)COC(C)=O URAYPUMNDPQOKB-UHFFFAOYSA-N 0.000 description 6
- 230000000996 additive effect Effects 0.000 description 5
- 239000007789 gas Substances 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 4
- 150000007513 acids Chemical class 0.000 description 4
- 125000000217 alkyl group Chemical group 0.000 description 4
- 125000004432 carbon atom Chemical group C* 0.000 description 4
- JQVDAXLFBXTEQA-UHFFFAOYSA-N dibutylamine Chemical compound CCCCNCCCC JQVDAXLFBXTEQA-UHFFFAOYSA-N 0.000 description 4
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 4
- 239000000835 fiber Substances 0.000 description 4
- 239000002245 particle Substances 0.000 description 4
- 238000009987 spinning Methods 0.000 description 4
- 239000012808 vapor phase Substances 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 230000002939 deleterious effect Effects 0.000 description 3
- 239000001087 glyceryl triacetate Substances 0.000 description 3
- 235000013773 glyceryl triacetate Nutrition 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 230000000391 smoking effect Effects 0.000 description 3
- 238000001179 sorption measurement Methods 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- 229960002622 triacetin Drugs 0.000 description 3
- SCOUYYCCBDRYLF-UHFFFAOYSA-N 2-(2-hydroxyethylamino)ethanol;2-hydroxypropane-1,2,3-tricarboxylic acid Chemical compound OCCNCCO.OC(=O)CC(O)(C(O)=O)CC(O)=O SCOUYYCCBDRYLF-UHFFFAOYSA-N 0.000 description 2
- PANKGRJVPCVYOA-UHFFFAOYSA-N C(C)(=O)[O-].[NH4+].C(C)O.C(C)O Chemical compound C(C)(=O)[O-].[NH4+].C(C)O.C(C)O PANKGRJVPCVYOA-UHFFFAOYSA-N 0.000 description 2
- RDOINTNNKBQCAS-UHFFFAOYSA-N C([O-])([O-])=O.[NH4+].C(C)O.C(C)O.[NH4+] Chemical compound C([O-])([O-])=O.[NH4+].C(C)O.C(C)O.[NH4+] RDOINTNNKBQCAS-UHFFFAOYSA-N 0.000 description 2
- 229920000742 Cotton Polymers 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- DMQBXILIOGFOOB-UHFFFAOYSA-N [NH4+].C(C)O.C(CC(O)(C(=O)[O-])CC(=O)[O-])(=O)[O-].[NH4+].[NH4+] Chemical compound [NH4+].C(C)O.C(CC(O)(C(=O)[O-])CC(=O)[O-])(=O)[O-].[NH4+].[NH4+] DMQBXILIOGFOOB-UHFFFAOYSA-N 0.000 description 2
- CBTVGIZVANVGBH-UHFFFAOYSA-N aminomethyl propanol Chemical compound CC(C)(N)CO CBTVGIZVANVGBH-UHFFFAOYSA-N 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- 239000001913 cellulose Substances 0.000 description 2
- 210000004081 cilia Anatomy 0.000 description 2
- 230000001419 dependent effect Effects 0.000 description 2
- QUSNBJAOOMFDIB-UHFFFAOYSA-O ethylaminium Chemical compound CC[NH3+] QUSNBJAOOMFDIB-UHFFFAOYSA-O 0.000 description 2
- IMTHXCRWRZBSKR-UHFFFAOYSA-N ethylazanium;2-methylidenebutanedioate Chemical compound CC[NH3+].CC[NH3+].[O-]C(=O)CC(=C)C([O-])=O IMTHXCRWRZBSKR-UHFFFAOYSA-N 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- BOQCCAZJWHZMBG-UHFFFAOYSA-N n-ethylethanamine;2-hydroxypropanoic acid Chemical compound CCNCC.CC(O)C(O)=O BOQCCAZJWHZMBG-UHFFFAOYSA-N 0.000 description 2
- 230000001473 noxious effect Effects 0.000 description 2
- 239000012071 phase Substances 0.000 description 2
- 239000004014 plasticizer Substances 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 150000000000 tetracarboxylic acids Chemical class 0.000 description 2
- 150000003628 tricarboxylic acids Chemical class 0.000 description 2
- 229940058020 2-amino-2-methyl-1-propanol Drugs 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 241000518994 Conta Species 0.000 description 1
- XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical compound N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 206010040880 Skin irritation Diseases 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- MQFIKAWTCOXAAY-UHFFFAOYSA-N acetic acid;n-butylbutan-1-amine Chemical compound CC([O-])=O.CCCC[NH2+]CCCC MQFIKAWTCOXAAY-UHFFFAOYSA-N 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 150000003973 alkyl amines Chemical class 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 239000012876 carrier material Substances 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 238000004737 colorimetric analysis Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000010410 dusting Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000002657 fibrous material Substances 0.000 description 1
- 239000000796 flavoring agent Substances 0.000 description 1
- 235000019634 flavors Nutrition 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000010907 mechanical stirring Methods 0.000 description 1
- 239000002808 molecular sieve Substances 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 235000019645 odor Nutrition 0.000 description 1
- 230000009965 odorless effect Effects 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 230000008520 organization Effects 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 239000012266 salt solution Substances 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 230000036556 skin irritation Effects 0.000 description 1
- 231100000475 skin irritation Toxicity 0.000 description 1
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 235000019505 tobacco product Nutrition 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
- A24D3/14—Use of materials for tobacco smoke filters of organic materials as additive
Definitions
- Tobacco smoke filtering mediums containing at least one amine salt for selectivity removing hydrogen cyanide from tobacco smoke.
- the particular salts are produced by reacting a primary alkyl or hydroxyalkyl amine conta ning no more than 8 carbon atoms with a carboxylic acid.
- Activated carbon does not remove cigarette smoke vapor selectively even though it has more afifinity for some vapor components than others.
- the adsorption of vapors by carbon is dependent upon the boiling point of the. vapor being adsorbed, that is, the least volatile vapors will be more readily adsorbed and retained by activated carbon addltives as opposed to the more volatile vapors.
- Th1s IS a definite disadvantage since several of the least volatile vapors in cigarette smoke are those which give flavor and taste to the smoke and are neither deleterious nor harmful to the smoker. Therefore, the removal of these vapors Patented Nov. 12, 1968 ICC is highly undesirable and if permitted to occur can result in what has commonly been referred to as a carbon or dry taste.
- the adsorption of vapors by carbon in a cigarette filter therefore is a physical phenomenon dependent upon temperature and pressure. Since the temperature of a cigarette filter increases as the burning zone of the cigarette approaches the filter during the smoking of a cigarette, the temperature of the carbon in the filter is raised causing the more volatile vapors adsorbed on the carbon to be eluted from the carbon. Thus, the carbon particles do not remove the more volatile vapors elfectively. In addition, as stated above, the less volatile gases which contribute to the taste and aroma of the smoke, and are generally neither deleterious or harmful, are also removed by carbon filters.
- carboxylic acid salts are prepared by reacting primary or secondary alkyl and hydroxyalkylamines containing no more than 8 carbon atoms with an acid.
- Some amines which have been found particularly eifective are: ethylamine, dibutylamine, 2-amino-2-methyl-l-propanol, ethanolamine, and diethanolamine.
- the acids used in the preparation of the salts can be mono-, di-, tri-, and tetracarboxylic acids which include the following: carbonic, acetic, itaconic, lactic, succinic, citric, and pyromellitic acids.
- filters incorporating these amine salts of a carboxylic acid provide a means for selectively removing hydrogen cyanide from cigarette smoke vapors without the use of activated carbons, silica gel, molecular sieve or other materials commonly used for the physical adsorption of vapor. It has been found that such acid salts are capable of chemically reacting on contact with the hydrogen cyanide vapor to neutralize the vapor thereby assuring that cyanide is not later released or otherwise eluted from the filter due to the increase in temperature of the filter during the smoking of the cigarette.
- such means employed for selectively removing hydrogen cyanide from the vapor phase of tobacco smoke does so without decreasing the capacity of the filter for removing solid particulate matter such as tar from the tobacco smoke.
- the additive for the filter element is an odorless, nonvolatile, nonirritant which can be applied to such materials as cellulose acetate without subsequent degradation of the material, it can be used freely without fear of its affecting the taste of the tobacco smoke or entering the smoke stream.
- the carboxylic acid salts of certain alkyl or hydroxyalkylamines may be applied by sifting, dusting, shaking, or from a plasticizer dispersion such as glyceryl triacetate. It may also be applied from any other suitable liquid by any convenient method such as by spraying or rolling on the carrier filter medium. Furthermore, more than one salt may be used as a mixture if desired.
- the fibrous media upon which the additives of this invention may be used is preferably a crimped continuous filament cellulose acetate tow, preferably of a denier per filament of about 1.620.
- such salts may be equally effectively employed upon filters which are made from other base materials such as paper, cotton, propylene and polyethylene fibers, or any other suitable material that can be formed into tobaco smoke filters.
- the carboxylic acid salts of aliphatic amines may be applied to the paper, tow or other carrier materials in the amount of from about 10-150 mg. (milligrams) per filter, the preferred amount being about 20 to 60 mg.
- the salt is enabled to take advantage of the large surface area which provides the contact necessaryy for effective hydrogen cyanide removal.
- a fibrous filtering unit which is capable of selectively removing hydrogen cyanide from a gaseous medium by spinning the fibers of the filter from a dope of cellulose acetate which contains an additive of the water-soluble, organic salts. Since these organic salts are embedded in the cellulose acetate fibers as the fibers are being spun, the necessity of including additional processing steps, materials and equipment into the manufacturing operation is alleviated.
- the selected Water-soluble salts if properly prepared, can be mixed with selective types of cellulose acetate dopes and spun to give a filament that readily neutralizes the hydrogen cyanide in tobacco smoke. It has been found, for example, rather unexpectedly that the salts are not masked by the acetate to a degree which would prevent their etfective removal of hydrogen cyanide when employed in tobacco smoke filters.
- the spinning solution or dope from which the filaments containing the organic salt are spun can be produced in any one of several manners. In its broadest aspect, this can be accomplished by adding directly to the cellulose acetate solution one or more of the carboxylic acid salts selected from the groups that are prepared from primary or secondary alkyl and hydroxyalkylamines which contain no more than 8 carbon atoms which are reacted with a suitable acid. More specifically, these salts are added to an acetone solution of cellulose acetone solution of cellulose acetate in the amount of from about to 30 percent based on weight of the cellulose acetate. After the carboxylic acid salts have been added to the acetone solution of cellulose acetate, the mix is uniformly dispersed. The spinning solution containing the carboxylic acid salt is now ready to be spun into filaments on a conventional spinning machine after which it can be formed into a tobacco smoke filter by any suitable manner.
- EXAMPLE I With methanol as sol-vent, a solution of ethanol ammonium citrate was prepared by adding a ratio of three moles ethanolamine to one mole of citric acid. The solution was added to commercial creped-paper filters and after evaporation of the methanol, the 10 mm. filters each contained 60 mg. of the salt.
- EXAMPLE II An aqueous solution of dibutylamine was titrated to neutrality with 5% aqueous acetic acid. The resulting salt solution was pipetted onto 10 mm. cellulose acetate filters such that each filter contained 60 mg. of the salt. When the filters were dry they were tested as in Example I. The elfect of this filter on the ciliatoxicity of tobacco smoke and its ability to remove HCN is shown in Table 1.
- EXAMPLE III Diethanol ammonium carbonate was prepared by adding 50 mg. diethanolamine in CH OH to a 20 mm. cellulose acetate filter and passing CO through the filter for twenty minutes. The filters were attached to cigarettes and tested as in Example I with the results being given in Table 1.
- EXAMPLE V Diethanol ammonium acetate, ethyl ammonium itaconate, 1,1-dimethyl ethanol ammonium malonate, ethyl ammonium pyromellitate and diethyl ammonium lactate were prepared as in Example I in a ratio of one amino group per carboxyi group. Crimped cellulose acetate tow was spread out to a length of approximately 15 in. The tow was sprayed with a 50-50 w./w.% aqueous solution of the salt and dried. The tow was then sprayed with triacetin, compacted, wrapped with a paper tape to form a rod and allowed to stand until firm. The triacetin cures the tow making a rigid rod and leaving the salt evenly distributed throughout the tow. After the rod became firm it was cut to a 20 mm. length and attached to a cigarette for testing as in Example I with the results being given in Table 1.
- a filter so produced is a highly selective one which is capable of removing substantial amounts of the solid particulate matter, such as tar, found in tobacco smoke as the smoke moves through the interstices of the filter, while at the same time selectively removing hydrogen cyanide from the vapor phase of the tobacco smoke by neutralizing or reducing it to a solid by-product which cannot later be eluted from the filter.
- the salt particles may also be embedded within the cellulose filaments of the filter eliminates sifting out and companion problems that have been heretofore present in filters containing solid additives.
- these amine salts may be incorporated in any of the known filter fibrous media used in the making of tobacco smoke filters such as, for example, cellulose acetate or paper.
- the hereinabove described method for the selective removal of hydrogen cyanide from the vaporous phase of tobacco smoke has been found to be both surprising and effective in its ability to remove this highly undesirable component from tobacco smoke and still provide the tobacco smoke with a taste and aroma most desirable for the ultimate smoker.
- a tobacco smoke filter element adapted for selective removal of deleterious and noxious materials from tobacco smoke which comprises a carrier medium having as an additive thereon at least one amine salt, said salt group consisting of primary alkyl amines and hydroxyalkyl amines containing no more than 8 carbon atoms with a carboxylic acid.
- a tobacco smoke filter of claim 1 wherein the amine is selected from the group consisting of ethylamine, 2- amino 2 methyl 1 propanol, ethanolamine, and diethanolamine.
- a tobacco smoke filter of claim 2 wherein the carboxylic acid is selected from the group consisting of carbonic, acetic, lactic, malonic, itaconic, succinic, citric, and pyromellitic acids.
- the tobacco smoke filter element of claim 1 wherein the carrier medium is selected from the group consisting of paper, cotton, cellulose acetate, polypropylene and polyethylene.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Cigarettes, Filters, And Manufacturing Of Filters (AREA)
Description
United States Patent 3,410,282 FILTER MEDIUM FOR REMOVING HYDROGEN CYANIDE FROM TOBACCO SMOKE Theodore Roosevelt Walker and John Edward Kiefer,
Kingsport, Tenn., assignors to Eastman Kodak Company, Rochester, N .Y., a corporation of New Jersey No Drawing. Filed Mar. 13, 1967, Ser. No. 622,470 6 Claims. (Cl. 131267) ABSTRACT OF THE DISCLOSURE Tobacco smoke filtering mediums containing at least one amine salt for selectivity removing hydrogen cyanide from tobacco smoke. The particular salts are produced by reacting a primary alkyl or hydroxyalkyl amine conta ning no more than 8 carbon atoms with a carboxylic acid.
It has been known for some time that tobacco smoke contains certain harmful components including hydrogen cyanide which, for obvious reasons, should be removed from tobacco smoke. It is well known, for example, that hydrogen cyanide is an extremely harmful ciliatoxic compound which contributes nothing beneficial to the pleasant taste or aroma of the smoke or to the smoker. It has therefore been the desire of the tobacco industry to provide an effective and practical tobacco smoke filter which is capable of selectively removing hydrogen cyanide from cigarette smoke without at the same time adversely affecting the pleasant taste and aroma found in the smoke.
The search for a suitable yet inexpensive filtermg medium which could be used with any tobacco product, and especially with cigarettes, led to the development of the so-called fibrous filter unit. These fibrous filters, and particularly those made of cellulose acetate tow, have been found to be very effective for removing solid particulate matter commonly referred to as tar from tobacco smoke. However, it is difiicult, if not impossible, to remove certain undesirable components, such as hydrogen cyanide, which is found in tobacco smoke by use of such filters.
It has been known that certain gas adsorbing additives in the form of finely divided particles can be dispersed within the fibrous filter for removing such undesirable gases. These particles of solid materials were generally placed on the surface of a fibrous material in either a dry or liquid state. Numerous solid adsorbing materials were tried with activated carbon and certain silica gels being the ones most often used.
However, there are certain limitations and disadvantages to using activated carbon in a cigarette filter for removing cigarette smoke vapors. Activated carbon does not remove cigarette smoke vapor selectively even though it has more afifinity for some vapor components than others. In general, the adsorption of vapors by carbon is dependent upon the boiling point of the. vapor being adsorbed, that is, the least volatile vapors will be more readily adsorbed and retained by activated carbon addltives as opposed to the more volatile vapors. Th1s IS a definite disadvantage since several of the least volatile vapors in cigarette smoke are those which give flavor and taste to the smoke and are neither deleterious nor harmful to the smoker. Therefore, the removal of these vapors Patented Nov. 12, 1968 ICC is highly undesirable and if permitted to occur can result in what has commonly been referred to as a carbon or dry taste.
The adsorption of vapors by carbon in a cigarette filter therefore is a physical phenomenon dependent upon temperature and pressure. Since the temperature of a cigarette filter increases as the burning zone of the cigarette approaches the filter during the smoking of a cigarette, the temperature of the carbon in the filter is raised causing the more volatile vapors adsorbed on the carbon to be eluted from the carbon. Thus, the carbon particles do not remove the more volatile vapors elfectively. In addition, as stated above, the less volatile gases which contribute to the taste and aroma of the smoke, and are generally neither deleterious or harmful, are also removed by carbon filters. Furthermore, since the removal of solid particulate matter commonly called tar is also of prime importance, cigarette filters containing activated carbon additives for the removal of vapors do not fulfill the requirement for the removal of solid particulate matter such as tar. Thus the problem of the tobacco industry; namely, how to economically produce a filter which is capable of selectively removing vapors such as hydrogen cyanide from the vapor phase of tobacco smoke, has todate remained unsolved.
It has been reported that certain amines when applied to cigarette filters remove noxious gases from the smoke more selectively than carbon; however, there are several decided disadvantages to their use in filters. For example, amines are notorious for their offensive odors and this property alone eliminates most of them from consideration Another disconcerting property of amines is their strong basicity which causes skin irritation; therefore if they are to be used in cigarette filters, they must be prevented from entering the smoke stream. Amine filters also tend to impart an off-taste to the smoke which may be due to the imbalance caused by absorption of acids by the amine. Furthermore, they cannot be used as additives to cellulose acetate, the most widely used filter medium, because they degrade it.
According to this invention it has been found that the aforementioned difficulties of the prior art tobacco smoke filters can be substantially overcome by the use of an amine salt of a carboxylic acid dispersed on a carrier inserted into a stream of tobacco smoke and arranged to provide interstices for the passage of smoke therethrough, serves to selectively remove hydrogen cyanide from the smoke. These carboxylic acid salts are prepared by reacting primary or secondary alkyl and hydroxyalkylamines containing no more than 8 carbon atoms with an acid. Some amines which have been found particularly eifective are: ethylamine, dibutylamine, 2-amino-2-methyl-l-propanol, ethanolamine, and diethanolamine. The acids used in the preparation of the salts can be mono-, di-, tri-, and tetracarboxylic acids which include the following: carbonic, acetic, itaconic, lactic, succinic, citric, and pyromellitic acids.
As will be apparent, filters incorporating these amine salts of a carboxylic acid provide a means for selectively removing hydrogen cyanide from cigarette smoke vapors without the use of activated carbons, silica gel, molecular sieve or other materials commonly used for the physical adsorption of vapor. It has been found that such acid salts are capable of chemically reacting on contact with the hydrogen cyanide vapor to neutralize the vapor thereby assuring that cyanide is not later released or otherwise eluted from the filter due to the increase in temperature of the filter during the smoking of the cigarette. Furthermore, such means employed for selectively removing hydrogen cyanide from the vapor phase of tobacco smoke does so without decreasing the capacity of the filter for removing solid particulate matter such as tar from the tobacco smoke. Since the additive for the filter element is an odorless, nonvolatile, nonirritant which can be applied to such materials as cellulose acetate without subsequent degradation of the material, it can be used freely without fear of its affecting the taste of the tobacco smoke or entering the smoke stream.
The carboxylic acid salts of certain alkyl or hydroxyalkylamines may be applied by sifting, dusting, shaking, or from a plasticizer dispersion such as glyceryl triacetate. It may also be applied from any other suitable liquid by any convenient method such as by spraying or rolling on the carrier filter medium. Furthermore, more than one salt may be used as a mixture if desired. The fibrous media upon which the additives of this invention may be used is preferably a crimped continuous filament cellulose acetate tow, preferably of a denier per filament of about 1.620. However, it will be appreciated that such salts may be equally effectively employed upon filters which are made from other base materials such as paper, cotton, propylene and polyethylene fibers, or any other suitable material that can be formed into tobaco smoke filters.
The carboxylic acid salts of aliphatic amines may be applied to the paper, tow or other carrier materials in the amount of from about 10-150 mg. (milligrams) per filter, the preferred amount being about 20 to 60 mg. By uniform application to the surface of the fibrous media the salt is enabled to take advantage of the large surface area which provides the contact necesary for effective hydrogen cyanide removal.
It also has been found that it is possible to produce a fibrous filtering unit which is capable of selectively removing hydrogen cyanide from a gaseous medium by spinning the fibers of the filter from a dope of cellulose acetate which contains an additive of the water-soluble, organic salts. Since these organic salts are embedded in the cellulose acetate fibers as the fibers are being spun, the necessity of including additional processing steps, materials and equipment into the manufacturing operation is alleviated. The selected Water-soluble salts, if properly prepared, can be mixed with selective types of cellulose acetate dopes and spun to give a filament that readily neutralizes the hydrogen cyanide in tobacco smoke. It has been found, for example, rather unexpectedly that the salts are not masked by the acetate to a degree which would prevent their etfective removal of hydrogen cyanide when employed in tobacco smoke filters.
The spinning solution or dope from which the filaments containing the organic salt are spun can be produced in any one of several manners. In its broadest aspect, this can be accomplished by adding directly to the cellulose acetate solution one or more of the carboxylic acid salts selected from the groups that are prepared from primary or secondary alkyl and hydroxyalkylamines which contain no more than 8 carbon atoms which are reacted with a suitable acid. More specifically, these salts are added to an acetone solution of cellulose acetone solution of cellulose acetate in the amount of from about to 30 percent based on weight of the cellulose acetate. After the carboxylic acid salts have been added to the acetone solution of cellulose acetate, the mix is uniformly dispersed. The spinning solution containing the carboxylic acid salt is now ready to be spun into filaments on a conventional spinning machine after which it can be formed into a tobacco smoke filter by any suitable manner.
The subject mater which is regarded as the invention is clearly pointed out and distinctly claimed in the concluding portion of the specification. The invention, however, as to its organization and operation, together with the further objects and advantages thereof will best be understood by reference to the following examples which are preferred embodiments of our invention.
EXAMPLE I With methanol as sol-vent, a solution of ethanol ammonium citrate was prepared by adding a ratio of three moles ethanolamine to one mole of citric acid. The solution was added to commercial creped-paper filters and after evaporation of the methanol, the 10 mm. filters each contained 60 mg. of the salt.
They were attached to king size cigarettes and the cigaretes smoked by an automatic smoking device which removed particulate matter from the smoke by means of a Cambridge filter. By a colorimetric test the smoke vapors were shown to contain 76% less HCN than vapors from an unfiltered cigarette smoked in the same manner.
In addition ciliatoxicity of the vapor phase of smoke from these filtered cigaretes was determined by the method which was described by Spears, Tryfiates, and Schultz at the 18th Tobacco Chemists Research Conference (1964) [see Science, 153, No. 3741, 1248 (1966)]. This method uses clam gill cilia as the test specimen. This test showed that the filter reduced ciliastasis of the gas phase of smoke by 80%.
EXAMPLE II An aqueous solution of dibutylamine was titrated to neutrality with 5% aqueous acetic acid. The resulting salt solution was pipetted onto 10 mm. cellulose acetate filters such that each filter contained 60 mg. of the salt. When the filters were dry they were tested as in Example I. The elfect of this filter on the ciliatoxicity of tobacco smoke and its ability to remove HCN is shown in Table 1.
EXAMPLE III Diethanol ammonium carbonate was prepared by adding 50 mg. diethanolamine in CH OH to a 20 mm. cellulose acetate filter and passing CO through the filter for twenty minutes. The filters were attached to cigarettes and tested as in Example I with the results being given in Table 1.
EXAMPLE IV Seven hundred grams (3 /3 moles) of citric acid was added slowly with mechanical stirring to a solution of ml. water in 1051 g. (10 moles) diethanolamine. An ice bath kept the temperature from rising above 50 C. The pH of this preparation was 7.3 measured as a 5% aqueous solution. Since diethanol ammonium citrate is a liquid, it was rolled onto cellulose acetate tow by a method'developed for the application of plasticizers. The effect of this filter on the ciliatoxicity of tobacco smoke and its ability to remove HCN is shown in Table 1.
EXAMPLE V Diethanol ammonium acetate, ethyl ammonium itaconate, 1,1-dimethyl ethanol ammonium malonate, ethyl ammonium pyromellitate and diethyl ammonium lactate were prepared as in Example I in a ratio of one amino group per carboxyi group. Crimped cellulose acetate tow was spread out to a length of approximately 15 in. The tow was sprayed with a 50-50 w./w.% aqueous solution of the salt and dried. The tow was then sprayed with triacetin, compacted, wrapped with a paper tape to form a rod and allowed to stand until firm. The triacetin cures the tow making a rigid rod and leaving the salt evenly distributed throughout the tow. After the rod became firm it was cut to a 20 mm. length and attached to a cigarette for testing as in Example I with the results being given in Table 1.
TABLE 1 Mg. Filter Inhibition of HCN Filter Additive Additive Medium Cilia Fre- Removal quency percent percent Ethanol ammonium citrate 62 Paper 5 76 Dibutyl ammonium acetate 60 Cellulose acetate. 0 85 Diethanol ammonium carbonate 74 d 8 89 Diethanol ammonium citrate 78 3 82 Ethyl ammonium itaconate 65 10 82 1,1-dimethyl ethanol ammonium malonat 71 12 79 Ethyl ammonium pyromellitate 78 8 85 Diethanol ammonium acetate 68 4 90 Diethyl ammonium lactate 65 8 80 None 0 Paper 62 0 Do 0 Cellulose acetate 58 0 Dom. 0 one 65 0 Carbon 113 Cellulose acetate 35 55 From the foregoing description and illustrative eX- 15 being produced by reacting an amine selected from the amples it is apparent the inventive concept of incorporating certain amine salts of organic acids with the fibrous carrier media of a tobacco smoke filter offers numerous de-toxicating advantages over those filters previously used in the tobacco industry. For example, a filter so produced is a highly selective one which is capable of removing substantial amounts of the solid particulate matter, such as tar, found in tobacco smoke as the smoke moves through the interstices of the filter, while at the same time selectively removing hydrogen cyanide from the vapor phase of the tobacco smoke by neutralizing or reducing it to a solid by-product which cannot later be eluted from the filter. Furthermore, the fact that the salt particles may also be embedded within the cellulose filaments of the filter eliminates sifting out and companion problems that have been heretofore present in filters containing solid additives. Furthermore, these amine salts may be incorporated in any of the known filter fibrous media used in the making of tobacco smoke filters such as, for example, cellulose acetate or paper. Thus, the hereinabove described method for the selective removal of hydrogen cyanide from the vaporous phase of tobacco smoke has been found to be both surprising and effective in its ability to remove this highly undesirable component from tobacco smoke and still provide the tobacco smoke with a taste and aroma most desirable for the ultimate smoker.
What is claimed and desired to be secured by the United States Letters Patent is:
1. A tobacco smoke filter element adapted for selective removal of deleterious and noxious materials from tobacco smoke which comprises a carrier medium having as an additive thereon at least one amine salt, said salt group consisting of primary alkyl amines and hydroxyalkyl amines containing no more than 8 carbon atoms with a carboxylic acid.
2. A tobacco smoke filter according to claim 1 in which the carboxylic acid is an acid selected from the group consisting of mono-, di-, tri-, or tetracarboxylic acids.
3. A tobacco smoke filter of claim 1 wherein the amine is selected from the group consisting of ethylamine, 2- amino 2 methyl 1 propanol, ethanolamine, and diethanolamine.
4. A tobacco smoke filter of claim 2 wherein the carboxylic acid is selected from the group consisting of carbonic, acetic, lactic, malonic, itaconic, succinic, citric, and pyromellitic acids.
5. The tobacco smoke filter element of claim 1 wherein the filter element contains from about 10-150 mg. of
, said salt per filter element.
6. The tobacco smoke filter element of claim 1 wherein the carrier medium is selected from the group consisting of paper, cotton, cellulose acetate, polypropylene and polyethylene.
References Cited UNITED STATES PATENTS 2,920,416 1/1960 Kinnavy 131-266 X 2,956,329 10/1960 Touey 131-266 X 2,968,306 1/1961 Touey et al 131266 3,127,901 4/ 1964 Whitefield et al 131267 3,144,024 8/1964 Eichwald et al. 131-267 3,246,655 4/1966 Spears et al 131--266 X SAMUEL KOREN, Primary Examiner.
DENNIS J. DONOHUE, Assistant Examiner.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US622470A US3410282A (en) | 1967-03-13 | 1967-03-13 | Filter medium for removing hydrogen cyanide from tobacco smoke |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US622470A US3410282A (en) | 1967-03-13 | 1967-03-13 | Filter medium for removing hydrogen cyanide from tobacco smoke |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3410282A true US3410282A (en) | 1968-11-12 |
Family
ID=24494286
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US622470A Expired - Lifetime US3410282A (en) | 1967-03-13 | 1967-03-13 | Filter medium for removing hydrogen cyanide from tobacco smoke |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US3410282A (en) |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3658070A (en) * | 1970-10-01 | 1972-04-25 | Nicholas R Diluzio | Tobacco smoke filters |
| US3716063A (en) * | 1970-09-25 | 1973-02-13 | Brown & Williamson Tobacco Corp | Selective gas phase filter material |
| USRE28858E (en) * | 1970-09-25 | 1976-06-15 | Brown & Williamson Tobacco Corporation | Selective gas phase filter material |
| US4022223A (en) * | 1973-07-26 | 1977-05-10 | Philip Morris Incorporated | Smoking article |
| EP0383018A3 (en) * | 1989-02-13 | 1990-11-07 | B.A.T. Cigarettenfabriken Gmbh | Process for impregnating tobacco smoke filter fibres with polycarboxylic acid or salts thereof |
| WO2002047498A1 (en) * | 2000-11-28 | 2002-06-20 | Lorillard Licensing Company, Llc | A smoking article including a filter for selectively removing carbonyls |
| US20080245376A1 (en) * | 2005-08-27 | 2008-10-09 | John Travers | Process For Making Filter Tow |
| CN103393219A (en) * | 2013-08-14 | 2013-11-20 | 中国烟草总公司郑州烟草研究院 | Modified natural plant filter tip additive material capable of selectively reducing burst size of hydrogen cyanide in main stream smoke of cigarettes and preparation method of modified natural plant filter tip additive material |
Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2920416A (en) * | 1958-07-23 | 1960-01-12 | Wallace A Erickson & Co | Treatment of tobacco smoke |
| US2956329A (en) * | 1954-12-15 | 1960-10-18 | Eastman Kodak Co | Manufacture of filamentary tobacco smoke filter |
| US2968306A (en) * | 1956-02-29 | 1961-01-17 | Eastman Kodak Co | Tobacco smoke filter capable of selective removal of aldehydes |
| US3127901A (en) * | 1960-07-22 | 1964-04-07 | Whitefield Harry | Absorbing composition for tobacco smoke |
| US3144024A (en) * | 1960-04-11 | 1964-08-11 | Darby Food Corp | Impregnated filter means for tobacco articles |
| US3246655A (en) * | 1963-03-19 | 1966-04-19 | Lorillard Co P | Selective cigarette filters |
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1967
- 1967-03-13 US US622470A patent/US3410282A/en not_active Expired - Lifetime
Patent Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2956329A (en) * | 1954-12-15 | 1960-10-18 | Eastman Kodak Co | Manufacture of filamentary tobacco smoke filter |
| US2968306A (en) * | 1956-02-29 | 1961-01-17 | Eastman Kodak Co | Tobacco smoke filter capable of selective removal of aldehydes |
| US2920416A (en) * | 1958-07-23 | 1960-01-12 | Wallace A Erickson & Co | Treatment of tobacco smoke |
| US3144024A (en) * | 1960-04-11 | 1964-08-11 | Darby Food Corp | Impregnated filter means for tobacco articles |
| US3127901A (en) * | 1960-07-22 | 1964-04-07 | Whitefield Harry | Absorbing composition for tobacco smoke |
| US3246655A (en) * | 1963-03-19 | 1966-04-19 | Lorillard Co P | Selective cigarette filters |
Cited By (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3716063A (en) * | 1970-09-25 | 1973-02-13 | Brown & Williamson Tobacco Corp | Selective gas phase filter material |
| USRE28858E (en) * | 1970-09-25 | 1976-06-15 | Brown & Williamson Tobacco Corporation | Selective gas phase filter material |
| US3658070A (en) * | 1970-10-01 | 1972-04-25 | Nicholas R Diluzio | Tobacco smoke filters |
| US4022223A (en) * | 1973-07-26 | 1977-05-10 | Philip Morris Incorporated | Smoking article |
| EP0383018A3 (en) * | 1989-02-13 | 1990-11-07 | B.A.T. Cigarettenfabriken Gmbh | Process for impregnating tobacco smoke filter fibres with polycarboxylic acid or salts thereof |
| WO2002047498A1 (en) * | 2000-11-28 | 2002-06-20 | Lorillard Licensing Company, Llc | A smoking article including a filter for selectively removing carbonyls |
| US6481442B1 (en) * | 2000-11-28 | 2002-11-19 | Lorillard Licensing Company, Llc | Smoking article including a filter for selectively removing carbonyls |
| US20080245376A1 (en) * | 2005-08-27 | 2008-10-09 | John Travers | Process For Making Filter Tow |
| US8308624B2 (en) * | 2005-08-27 | 2012-11-13 | Celanese Acetate Limited | Process for making filter tow |
| CN103393219A (en) * | 2013-08-14 | 2013-11-20 | 中国烟草总公司郑州烟草研究院 | Modified natural plant filter tip additive material capable of selectively reducing burst size of hydrogen cyanide in main stream smoke of cigarettes and preparation method of modified natural plant filter tip additive material |
| CN103393219B (en) * | 2013-08-14 | 2014-09-24 | 中国烟草总公司郑州烟草研究院 | Modified natural plant filter tip additive material capable of selectively reducing burst size of hydrogen cyanide in main stream smoke of cigarettes and preparation method of modified natural plant filter tip additive material |
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