Classifications

• • A—HUMAN NECESSITIES
  • A24—TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
  • A24B—MANUFACTURE OR PREPARATION OF TOBACCO FOR SMOKING OR CHEWING; TOBACCO; SNUFF
  • A24B15/00—Chemical features or treatment of tobacco; Tobacco substitutes, e.g. in liquid form
  • A24B15/18—Treatment of tobacco products or tobacco substitutes
  • A24B15/28—Treatment of tobacco products or tobacco substitutes by chemical substances
  • A24B15/30—Treatment of tobacco products or tobacco substitutes by chemical substances by organic substances

Definitions

• a smoking mixture comprises solid combustible material other than tobacco and as a flavourant a compound of the formula wherein X represents the atoms necessary to complete a carbocyclic or heterocyclic ring of or 6 carbon atoms and X represents an alkyl radical preferably of l to 4 carbon atoms.
• the solid combustible material may be a smokeproducing carbohydrate, for example a-cellulose, a cellulose ether e.g. methylcellulose, hydroxyethyl cellulose or carboxymethyl cellulose or a modified cellulose e.g. an oxidised cellulose. It may also be a sugar, starch, alginate, pectine or a natural gum.
• the solid combustible material is a thermally degraded carbohydrate, especially thermally degraded cellulose, manufactured for example by the process described and claimed in our UK. Pat. No. 1,1 13,979 by subjecting carbohydrate to catalysed degradation at 100 to 250C until the weight of degraded material is less than 90 percent of the dry weight of the original carbohydrate.
• Preferred degradation catalysts in such a process include sulphuric acid, sulphamic acid and ammonium sulphamare.
• the solid combustible material may also be a condensation product manufactured by acid or base catalysed condensation of a compound of the formula R COCH .CH COR (or a precursor thereof) wherein R and R which may be the same or different, each represents a hydrogen atom or an alkyl, hydroxyalkyl or formyl group.
• R and R which may be the same or different, each represents a hydrogen atom or an alkyl, hydroxyalkyl or formyl group.
• Preferred such products are condensates of succinaldehyde or acetonyl acetone or a condensate from a precursor of (l) containing a furan ring structure.
• the smoking mixtures may also contain other ingredients such as are normally used to impart desired physical properties and burning characteristics for example inorganic fillers, binders, plasticise'rs, humectants, colorants, glow-controlling catalysts, ash improv- 2 ers, nicotine, medicaments, and other flavourants besides those of the formulae (A) or (B).
• ingredients such as are normally used to impart desired physical properties and burning characteristics for example inorganic fillers, binders, plasticise'rs, humectants, colorants, glow-controlling catalysts, ash improv- 2 ers, nicotine, medicaments, and other flavourants besides those of the formulae (A) or (B).
• (A) for the flavourant compound heterocyclic rings completed by the atoms represented by X are preferably furan or pyran rings.
• flavourant compounds of for mula (A) are:
• corylone (Z-hydroxy-3-methyl-2-cyclopenten-l-one) malton (3-hydroxy-2-methyl-pyran-4-one) dihydromaltol (3-hydroxy-2-methyl( 5,6H-)pyran- 4-one) ethylmaltol (3-hydroxy-2-ethyl-pyran-4-one) a-hydroxy-B-methyl-y-hexen
• a specific example of a flavourant compound of formula (B) is isomaltol (3-hydroxy-2-acetyl-furan).
• flavourant compound may be incorporated with the solid combustible material by any desired technique.
• a solution of the flavourant compound in a volatile solvent may be sprayed on to the combustible material formulated with other ingredients into film or shred form.
• the smoke from the smoking mixture of the invention is more tobaccolike in flavour than that from the solid combustible material alone.
• the proportion of the said flavourant required to produce the tobacco-like flavour is small, generally less than 2% by weight.
• maltol, isomaltol, dihydromaltol and ethylmaltol are preferably used at 0.7 to 1.5 percent by weight.
• Corylone however is a much stronger flavourant and is preferably used in proportions of 0.01 to 0.3 percent by weight.
• the smoking mixtures may be blended with tobacco, for example in proportions containing up to 50 percent of tobacco.
• Such blends are less hazardous to health than the tobacco, when this is smoked alone, and are preferably in flavour to the corresponding blends containing no flavourant compound.
• EXAMPLE 1 9 parts of glycerol and 2 parts of ammonium sulphate were dissolved in 400 parts of water. 12 parts of SCMC were added to the stirred solution and stirring continued for ten minutes. To this stirred solution was added a mixture of 28.6 parts of magnesite, 16.5 parts of calcium carbonate, 5 parts of bentonite and 26.9 parts of a material prepared by heat treating a-cellulose in the presence of ammonium sulphamate until a weight loss of 25% occurred. Stirring was continued for at least one hour.
• the resulting slurry was cast on glass plates to give a film with a dry basis weight of 48-52 grams per sq.metre.
• the film was shredded and sprayed with 0.01 parts of corylone (2-hydroxy-3-methyl-2-cyclopentenl-one) in diethyl ether solution.
• the ether was evaporated off, the shred humidified and blended with its own weight of flue cured Virginian Tobacco. This blend was made into cigarettes.
• Example 1 was repeated using 0.05 parts corylone.
• EXAMPLE 3 8.7 parts of glycerol and 2 parts of ammonium sulphate were dissolved in 360 parts of water. 1 1.6 parts of SCMC were added to the stirred solution and stirring continued for minutes. Thereafter a solution of 3- parts of l-nicotine and 3 parts of lactic acid in 40 parts of water was added with stirring followed by the addition of a mixture of 26 parts of magnesite, 14.7 parts.
• the resulting slurry was cast on glass plates to give a film with a dry basis weight of 48-52 grams per sq.metre.
• the film was shredded and sprayed with 0.01 parts of corylone in diethyl ether solution.
• the ether was removed by evaporation, the shred humidified and blended with its own weight of Flue-cured Virginian tobacco. This blend was made into cigarettes.
• EXAMPLE 4 5.32 parts of a material prepared by heat treating a-cellulose in the presence of ammonium sulphamate until a weight loss of 25 percent occurred was mixed with 60 parts of water and ground in a disintegrator. 1.18 parts of glycerol followed by 0.2 parts of maltol and 0.4 parts of ammonium sulphate in 20 parts of water were added to the stirred mix. A dry mixture consisting of 3.28 parts of calcium carbonate and 0.98 parts of bentonite was then added bollowed by 2.98 parts of sodium carboxymethyl cellulose and 5.66 parts of magnesite and the resultant slurry stirred for at least 1 hour. The slurry was then cast to give a film with a dry basis weight of 48-52 grams per sq. metre.
• the film was shredded and the shred blended with flue-cured tobacco to give a blend containing 50 percent of tobacco.
• the blend was made up into cigarettes. v
• a similar flavour is produced by using isomaltol, dihydromaltol, ethylmaltol or Z-hydroxy-B-methylyhexenolactone in place of maltol.
• a smoking mixture comprising a thermally degraded carbohydrate tobacco substitute and, as a flavourant, a compound of the formula wherein X represents the atoms necessary to complete a carbocyclic or heterocyclic ring of 5 or 6 carbon atoms and X represents an alkyl radical preferably of 1 to 4 carbon atoms said thermally degraded carbohydrate being obtained by subjecting a carbohydrate material to a catalysed degradation process at a temperature of at least 100C until the weight of the degraded material is approximately percent or less of the dry weight of the original carbohydrate.
• a smoking mixture according to claim 1 wherein the solid combustible material is a thermally degraded cellulose.
• flavourant is corylone

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• Health & Medical Sciences (AREA)
• General Health & Medical Sciences (AREA)
• Toxicology (AREA)
• Chemical & Material Sciences (AREA)
• Chemical Kinetics & Catalysis (AREA)
• General Chemical & Material Sciences (AREA)
• Manufacture Of Tobacco Products (AREA)
• Paper (AREA)

Priority Applications (1)

Applications Claiming Priority (1)

Publications (1)

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Citations (4)

• 1971
  • 1971-12-15 GB GB5823071A patent/GB1364103A/en not_active Expired
• 1972
  • 1972-11-22 US US308743A patent/US3884245A/en not_active Expired - Lifetime
  • 1972-12-08 DE DE2260283A patent/DE2260283A1/de active Pending
  • 1972-12-14 JP JP47125770A patent/JPS4867500A/ja active Pending
  • 1972-12-15 CA CA159,170A patent/CA970644A/en not_active Expired

Patent Citations (4)

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