EP4146018A1 - Matériau de génération d'aérosol - Google Patents

Matériau de génération d'aérosol

Info

Publication number
EP4146018A1
EP4146018A1 EP21726696.4A EP21726696A EP4146018A1 EP 4146018 A1 EP4146018 A1 EP 4146018A1 EP 21726696 A EP21726696 A EP 21726696A EP 4146018 A1 EP4146018 A1 EP 4146018A1
Authority
EP
European Patent Office
Prior art keywords
generating material
aerosol generating
aerosol
particles
active substance
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
EP21726696.4A
Other languages
German (de)
English (en)
Inventor
Biniam TESFATSION
David Bishop
Simon Poynton
Tatiana BETSON
Ugurhan Yilmaz
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Nicoventures Trading Ltd
Original Assignee
Nicoventures Trading Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Nicoventures Trading Ltd filed Critical Nicoventures Trading Ltd
Publication of EP4146018A1 publication Critical patent/EP4146018A1/fr
Pending legal-status Critical Current

Links

Classifications

    • A—HUMAN NECESSITIES
    • A24—TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
    • A24C—MACHINES FOR MAKING CIGARS OR CIGARETTES
    • A24C5/00—Making cigarettes; Making tipping materials for, or attaching filters or mouthpieces to, cigars or cigarettes
    • A24C5/01—Making cigarettes for simulated smoking devices
    • 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
    • A24B15/10—Chemical features of tobacco products or tobacco substitutes
    • A—HUMAN NECESSITIES
    • A24—TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
    • A24B—MANUFACTURE OR PREPARATION OF TOBACCO FOR SMOKING OR CHEWING; TOBACCO; SNUFF
    • A24B13/00—Tobacco for pipes, for cigars, e.g. cigar inserts, or for cigarettes; Chewing tobacco; Snuff
    • A24B13/02—Flakes or shreds of tobacco
    • 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
    • A24B15/10—Chemical features of tobacco products or tobacco substitutes
    • A24B15/12—Chemical features of tobacco products or tobacco substitutes of reconstituted tobacco
    • A24B15/14—Chemical features of tobacco products or tobacco substitutes of reconstituted tobacco made of tobacco and a binding agent not derived from tobacco
    • 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
    • A24B15/186—Treatment of tobacco products or tobacco substitutes by coating with a coating composition, encapsulation of tobacco particles
    • 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
    • A24B15/281—Treatment of tobacco products or tobacco substitutes by chemical substances the action of the chemical substances being delayed
    • 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
    • A24B15/285—Treatment of tobacco products or tobacco substitutes by chemical substances characterised by structural features, e.g. particle shape or size
    • 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
    • A24B15/301—Treatment of tobacco products or tobacco substitutes by chemical substances by organic substances by aromatic compounds
    • 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
    • A24B15/302—Treatment of tobacco products or tobacco substitutes by chemical substances by organic substances by natural substances obtained from animals or plants
    • 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
    • A24B15/302—Treatment of tobacco products or tobacco substitutes by chemical substances by organic substances by natural substances obtained from animals or plants
    • A24B15/303—Plant extracts other than tobacco
    • 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
    • A24B15/34—Treatment of tobacco products or tobacco substitutes by chemical substances by organic substances containing a carbocyclic ring other than a six-membered aromatic ring
    • 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
    • A24B15/42—Treatment of tobacco products or tobacco substitutes by chemical substances by organic and inorganic substances
    • 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
    • A24D1/00—Cigars; Cigarettes
    • A24D1/20—Cigarettes specially adapted for simulated smoking devices
    • A—HUMAN NECESSITIES
    • A24—TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
    • A24F—SMOKERS' REQUISITES; MATCH BOXES; SIMULATED SMOKING DEVICES
    • A24F40/00—Electrically operated smoking devices; Component parts thereof; Manufacture thereof; Maintenance or testing thereof; Charging means specially adapted therefor
    • A24F40/10—Devices using liquid inhalable precursors
    • A—HUMAN NECESSITIES
    • A24—TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
    • A24F—SMOKERS' REQUISITES; MATCH BOXES; SIMULATED SMOKING DEVICES
    • A24F40/00—Electrically operated smoking devices; Component parts thereof; Manufacture thereof; Maintenance or testing thereof; Charging means specially adapted therefor
    • A24F40/20—Devices using solid inhalable precursors
    • A—HUMAN NECESSITIES
    • A24—TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
    • A24F—SMOKERS' REQUISITES; MATCH BOXES; SIMULATED SMOKING DEVICES
    • A24F40/00—Electrically operated smoking devices; Component parts thereof; Manufacture thereof; Maintenance or testing thereof; Charging means specially adapted therefor
    • A24F40/30—Devices using two or more structurally separated inhalable precursors, e.g. using two liquid precursors in two cartridges

Definitions

  • the invention relates to aerosol generating material for inclusion in an aerosol provision system, such as an apparatus for heating aerosol generating material to volatilise at least one component of the aerosol generating material, the aerosol generating material including an active substance and a volatile component incorporated by infusion.
  • an aerosol provision system such as an apparatus for heating aerosol generating material to volatilise at least one component of the aerosol generating material, the aerosol generating material including an active substance and a volatile component incorporated by infusion.
  • the invention also relates to methods for preparing such compositions.
  • Smoking articles such as cigarettes, cigars and the like burn tobacco during use to create tobacco smoke. Attempts have been made to provide alternatives to these articles by creating products that release compounds without combusting. Examples of such products are so-called “heat not burn” products or tobacco heating devices or products, which release compounds by heating, but not burning, smokeable material.
  • flavours in smoking articles to add specific desirable flavours to the aerosol generated by the smoking article. This has been achieved in a variety of different ways, including the use of crushable capsules that contain flavour compositions.
  • an aerosol generating material comprising at least one particle comprising an active substance, and a volatile component, wherein the volatile component has a vapour pressure at 20°C which is greater than or equal to the vapour pressure of the active substance at 20°C, wherein the volatile component is incorporated into the aerosol generating material by infusion, and wherein the release of the active substance from the aerosol generating material is controlled by competition with the release of the volatile component.
  • the aerosol generating material is for inclusion in an aerosol provision system.
  • the active substance is nicotine.
  • the particles comprising the active substance are tobacco particles.
  • the vapour pressure of the volatile component is at least 6 Pa at 20°C.
  • the volatile component is a volatile flavour.
  • the volatile component is selected from the group consisting of menthol, limonene, linalool, camphene and eucalyptol.
  • the volatile component does not have a distinctive or characteristic flavour.
  • the pH of the aerosol generating material is from about 4 to about 9.5.
  • the pH of the aerosol generating material is increased by the addition of one or more bases or a basic buffer system.
  • the one or more base is selected from the group consisting of hydroxides, carbonates and hydrogen carbonates, optionally wherein the one or more base is selected from the group consisting of: potassium hydroxide, sodium hydroxide, sodium carbonate and sodium bicarbonate.
  • the particles comprising an active substance have an average diameter no greater than 3 mm, no greater than 1 mm, no greater than 0.5 mm, or no greater than 0.3 mm.
  • the aerosol generating material further comprises one or more aerosol forming agent.
  • the aerosol forming agent is selected from the group consisting of glycerol, propylene glycol and glyceryl triacetate.
  • the aerosol generating material further comprises one or more binder.
  • the one or more binder is selected from the group consisting of: thermoreversible gelling agents, such as gelatin; starches; polysaccharides; pectins; celluloses; cellulose derivatives, such as carboxymethylcellulose; and alginates.
  • a precursor composition comprising the particles comprising an active substance is granulated or spheronised to form an agglomerated structure.
  • a precursor composition comprising the particles comprising an active substance is extruded to form an agglomerated structure.
  • the aerosol generating material is in the form of granules.
  • an aerosol provision system comprising an aerosol generating material according to the first aspect.
  • the system is an aerosol generating material heating system comprising an aerosol generating material which is to be heated to volatilise constituents, and optionally including a filter or filter element.
  • the system is a hybrid system comprising an aerosol generating material which is to be heated to volatilise constituents, and a liquid which is to be heated to form a vapour, and optionally including a filter or filter element.
  • the aerosol generating material consists of one or more particles of aerosol generating material.
  • the aerosol generating material is heated by the vapour.
  • the liquid is a nicotine-free liquid.
  • the device includes a means for heating the liquid to form a vapour, but does not include a separate means for heating the aerosol generating material.
  • a method for preparing an aerosol generating material comprising particles comprising an active substance and a volatile component for use in an aerosol provision system, the method comprising forming an agglomerated structure comprising the particles comprising an active substance and incorporating the volatile component into the agglomerated structure by infusion, wherein the volatile component has a vapour pressure at 20°C which is greater than or equal to the vapour pressure of the active substance at 20°C.
  • the aerosol generating material is formed from a precursor composition comprising particles comprising an active substance and resultant composition is infused with the volatile component.
  • the precursor composition is granulated or spheronised to form the agglomerated structure.
  • the precursor composition is extruded to form the agglomerated structure.
  • an apparatus for heating aerosol generating material to volatilise at least one component of the aerosol generating material, and a nicotine-free liquid which is to be heated to form a vapour wherein the aerosol generating material comprises a aerosol generating material according to the first aspect, and wherein the aerosol generating material is heated by the vapour.
  • the apparatus includes a means for heating the liquid to form a vapour, but not including a separate means for heating the aerosol generating material.
  • the pH is increased by the addition of one or more bases or a basic buffer system.
  • a particle incorporating a volatile component by infusion wherein the volatile component has a vapour pressure at 20°C which is greater than or equal to the vapour pressure of the active substance at 20°C, for use in controlling the release of nicotine in an aerosol generating material.
  • Figure 1 is a flow chart showing key steps of a process according to embodiments of the present invention
  • Figure 2 is a schematic representation of some extruded granules
  • Figure 3 is a schematic cross-sectional view of a product for heating aerosol generating material to volatilise at least one component of the aerosol generating material;
  • Figure 4 is a schematic view of a hybrid system for heating aerosol generating material to volatilise at least one component of the aerosol generating material; and
  • Figure 5 is a schematic cross-sectional view of an example of a cartridge containing multiple particles of aerosol generating material.
  • the invention relates to an aerosol generating material comprising and active substance and a volatile component added to the composition by infusion.
  • the composition is able to release the volatile component and active substance when heated.
  • the aerosol generating material is in particulate or monolithic form.
  • the material is an agglomerated structure. This means that they are a mass or cluster formed by fusing or adhering multiple particles to one another.
  • the aerosol generating material is able to provide a consistent and extended release of the active substance from the aerosol generating material as a result of the presence of a volatile component that has a vapour pressure at 20°C that is greater than or equal to the vapour pressure of the active substance at 20°C.
  • a volatile component that has a vapour pressure at 20°C that is greater than or equal to the vapour pressure of the active substance at 20°C.
  • the active substance and volatile component compete to volatise from the aerosol generating material.
  • the presence of the volatile component which is readily volatilised upon heating is thought to supress the volatilisation of the active substance, slowing its release from the aerosol generating material.
  • the active substance such as nicotine
  • the active substance is generally seen to be rapidly volatilise, providing an initial rapid release of the active substance which is then followed by a sharp drop off in nicotine release, leading to an inconsistent delivery and user experience. Therefore, in some embodiments of the invention, the presence of the volatile component controls the release of the active substance(s) from the aerosol generating material. This is an unexpected and highly beneficial effect of the compositions described herein.
  • the composition comprises a volatile component added by infusion. Upon heating of the infused aerosol generating material, the volatile component within the porous surface of the material is released for delivery in the aerosol generated by heating the aerosol generating material.
  • the aerosol generating material is infused with the volatile component.
  • the volatile component is transferred during infusion and is provided in pores of the particles of the aerosol generating material.
  • the process of infusion depends upon the low vapour pressure and/or high volatility of the volatile component that is provided in either solid form or liquid form.
  • the volatile component volatilises from the solid or liquid form.
  • the volatilised volatile component is deposited on the surface of the material, and in particular in the pores of the material, thus forming an aerosol generating material that has been infused with the volatile component.
  • the active substance as used herein may be a physiologically active material, which is a material intended to achieve or enhance a physiological response.
  • the active substance may for example be selected from nutraceuticals, nootropics, psychoactives.
  • the active substance may be naturally occurring or synthetically obtained.
  • the active substance may comprise for example nicotine, caffeine, taurine, theine, vitamins such as B6 or B12 or C, melatonin, cannabinoids, or constituents, derivatives, or combinations thereof.
  • the active substance may comprise one or more constituents, derivatives or extracts of tobacco, cannabis or another botanical.
  • the active substance comprises nicotine.
  • the active substance comprises caffeine, melatonin or vitamin B12.
  • the active substance may comprise or be derived from one or more botanicals or constituents, derivatives or extracts thereof.
  • botanical includes any material derived from plants including, but not limited to, extracts, leaves, bark, fibres, stems, roots, seeds, flowers, fruits, pollen, husk, shells or the like.
  • the material may comprise an active compound naturally existing in a botanical, obtained synthetically. The material maybe in the form of liquid, gas, solid, powder, dust, crushed particles, granules, pellets, shreds, strips, sheets, or the like.
  • Example botanicals are tobacco, eucalyptus, star anise, hemp, cocoa, cannabis, fennel, lemongrass, peppermint, spearmint, rooibos, chamomile, flax, ginger, ginkgo biloba, hazel, hibiscus, laurel, licorice (liquorice), matcha, mate, orange skin, papaya, rose, sage, tea such as green tea or black tea, thyme, clove, cinnamon, coffee, aniseed (anise), basil, bay leaves, cardamom, coriander, cumin, nutmeg, oregano, paprika, rosemary, saffron, lavender, lemon peel, mint, juniper, elderflower, vanilla, wintergreen, beefsteak plant, curcuma, turmeric, sandalwood, cilantro, bergamot, orange blossom, myrtle, cassis, valerian, pimento, mace, damien, marjoram, olive, lemon
  • the mint may be chosen from the following mint varieties: Mentha Arventis, Mentha c.v., Mentha niliaca, Mentha piperita, Mentha piperita citrata c.v., Mentha piperita c.v, Mentha spicata crispa, Mentha cardifolia, Mentha longifolia, Mentha suaveolens variegata, Mentha pulegium, Mentha spicata c.v. and Mentha suaveolens
  • the active substance comprises or is derived from one or more botanicals or constituents, derivatives or extracts thereof and the botanical is tobacco. In some embodiments, the active substance comprises or is derived from one or more botanicals or constituents, derivatives or extracts thereof and the botanical is selected from eucalyptus, star anise, cocoa and hemp.
  • the active substance comprises or is derived from one or more botanicals or constituents, derivatives or extracts thereof and the botanical is selected from rooibos and fennel. Particles of active substance
  • the aerosol generating material comprises a particle or particles comprising an active substance.
  • particles of an active substance are also referred to as “active particles”.
  • the active substance is a plant derived active substance.
  • the particles of active substance maybe plant particles comprising the active substance.
  • the particles of active substance may comprise the active substance deposited in or on particles of carrier material.
  • the active substance is nicotine.
  • the nicotine particles may be particles of tobacco material.
  • the nicotine particles may comprise a carrier material and nicotine.
  • the particles comprising the active substance present in the aerosol generating material have a size small enough to ensure that multiple such particles can be agglomerated to form an aerosol provision system having desired dimensions based upon their intended use.
  • Smaller particles of active substance have a greater surface area to volume ratio and they may therefore exhibit enhanced release of the active substance compared to particles of larger sizes.
  • the size of the active particles (and of other particles in the precursor composition) will have an effect on the porosity and density of the agglomerated structures and the aerosol generating material.
  • the size of the active particles maybe selected to produce a more porous agglomerated structure, which will have an impact on the release of the active substance.
  • the size of the active particles is another factor that may be adjusted in order to influence the release of the active substance, in particular where the aerosol generating material has an agglomerated structure made by granulation as opposed to extrusion.
  • the preferred size of the active particles may also depend upon the method used to form the agglomerated structures.
  • extrusion processes can be sensitive to the size of the particles within the composition being extruded.
  • the particles in the precursor composition, including the active particles, such as tobacco particles it maybe desirable for the particles in the precursor composition, including the active particles, such as tobacco particles, to have an average particle size of no greater than about 3 mm, of no greater than 1 mm, of no greater than about 0.5 mm, or to have an average particle size of no greater than about 0.3 mm, when measured by sieving.
  • the active particles in the precursor composition and/or in the aerosol generating material may be desirable for the active particles in the precursor composition and/or in the aerosol generating material to have an average particle size of no greater than about 3 mm, of no greater than 1 mm, of no greater than about 0.5 mm, or to have an average particle size of no greater than about 0.3 mm, when measured by sieving.
  • the average particle size is within the range of about 0.1 to about 3 mm, of about 0.1 to about 1 mm, of about 0.1 to about 0.5 mm, of about 0.1 to about 0.4 mm, or in the range of about 0.2 to about 0.3 mm.
  • At least about 90% of the particles of the precursor composition will have a particle size within the range of about 0.1 to about 3 mm, or of about 0.1 to about 1 m, or of about 0.1 to about 0.5 mm. In some embodiments, at least about 90% of the active particles of the precursor composition will have a particle size within the range of about 0.1 to about 3 mm, or of about 0.1 to about 1 mm, or of about 0.1 to 0.5 mm. In some embodiments, none of the particles in the precursor composition have a particle size greater than 5 mm, greater than 4 mm, greater than 2 mm, greater than 1.5 mm, or greater than about 1 mm.
  • the active particles are particles of plant material. Where the active substance is or includes nicotine, the active particles may be particles of tobacco material (referred to herein as tobacco particles).
  • Particles of the desired size may be formed by grinding, shredding, cutting or crushing plant material such as tobacco material.
  • Suitable machinery to create such plant particles includes, for example, shredders, cutters, or mills, such as hammer mills, roller mills or other types of commercially available milling machinery.
  • the size of the plant particles is selected to provide particles which can be readily prepared from a variety of different types of plant material, which can be formed into agglomerated structures using the processes described herein and having the properties described herein, and which provide a source of active substances that are readily released.
  • the chopping of the tobacco to form the tobacco particles enhances the release of tobacco constituents including volatile flavours and aromatic constituents, as well as nicotine.
  • the increased surface area of the tobacco particles is also thought to aid volatilisation.
  • the smaller tobacco particles also improve the homogeneity of agglomerated structures formed therefrom together with other components.
  • the tobacco material used to form the tobacco particles may be any type of tobacco and any part of the tobacco plant, including tobacco lamina, stem, stalk, ribs, scraps and shorts or mixtures of two or more thereof. Suitable tobacco materials include the following types: Virginia or flue-cured tobacco, Burley tobacco, Oriental tobacco, or blends of tobacco materials, optionally including those listed here.
  • the tobacco may be expanded, such as dry-ice expanded tobacco (DIET), or processed by any other means.
  • the tobacco material may be reconstituted tobacco material.
  • the tobacco may be pre-processed or unprocessed, and may be, for instance, solid stems (SS); shredded dried stems (SDS); steam treated stems (STS); or any combination thereof.
  • the tobacco material may be fermented, cured, uncured, toasted, or otherwise pre-treated. pH Adjustment
  • the aerosol generating material is formed from a precursor composition comprising the active particles, wherein the pH of the active particles has been adjusted to a basic pH.
  • the pH maybe adjusted to at least about 7.5.
  • the pH may be adjusted by the addition of one or more bases.
  • the pH may be adjusted by the use of a buffer solution.
  • the active substance in the pH-adjusted material is nicotine.
  • the aerosol generating material comprises active particles and one or more bases or a basic buffer system, so that the nicotine particles have a basic pH.
  • the pH may be at least about 7.5.
  • the purpose of adjusting the pH of the active particles and/or of the precursor composition is to provide the active substance in a chemical form that is readily released from the aerosol generating material, and/or they are readily transferred to the aerosol generated by the smoking article.
  • the pH of the active particles is adjusted to at least about 7.5, at least about 8, at least about 8.5, at least about 9, at least about 9.5 or at least about 10.
  • the pH is adjusted to no higher than about 14, no higher than about 13.5, no higher than about 13, no higher than about 12.5, no higher than about 12, no higher than about 11.5, no higher than about 11, no higher than about 10.5 or no higher than about 10.
  • the pH of the active particles is adjusted to from about 8 to about 10, or from about 8.5 to about 9.5.
  • the pH of the aerosol generating material is at least about 7.5, at least about 8, at least about 8.5, at least about 9, at least about 9.5 or at least about 10. In some embodiments, the pH is no higher than about 14, no higher than about 13.5, no higher than about 13, no higher than about 12.5, no higher than about 12, no higher than about 11.5, no higher than about 11, no higher than about 10.5 or no higher than about 10. In some embodiments, the pH of the aerosol generating material is adjusted to from about 8 to about 10, or from about 8.5 to about 9.5.
  • the pH of the aerosol generating material is adjusted to from about 7.5 to about 10, or from about 8 to about 9, or to about 8.5, about 9, about 9.5 or about 10.
  • the base used to adjust the pH is a hydroxide or a carbonate.
  • Hydroxides used may be monoacidic bases, diacidic bases or triacidic bases.
  • Suitable bases include, for example, potassium hydroxide, calcium hydroxide, silver hydroxide, ammonium hydroxide, magnesium hydroxide, sodium carbonate, sodium bicarbonate (also known as sodium hydrogen carbonate), and potassium carbonate.
  • the base may be added in the form of a liquid, such as an aqueous or non-aqueous solution or suspension, or in the form of a solid, such as a powder.
  • a liquid such as an aqueous or non-aqueous solution or suspension
  • a solid such as a powder.
  • the pH of the particles comprising a volatile component is not adjusted.
  • the aerosol generating material is formed from a precursor composition comprising particles comprising an active substance.
  • the precursor composition further comprises a pH adjuster.
  • the pH of the precursor composition will be adjusted (compared to the pH of the particles without the pH adjuster) once water is added to the composition.
  • the pH of the precursor composition or of the aerosol generating material refers to the pH once water is added to the composition where the composition is dry.
  • the buffer system used to adjust the pH is a mixture of a weak base and its conjugate acid.
  • Suitable buffer systems include, for example, ones having a pH of at least about 7.5, at least about 8, at least about 8.5 or at least about 9.
  • the pH of the buffer system is from about 8 to about 10, or from about 8.5 to about 9.5.
  • Suitable buffer systems include, for example, those based on ammonia, carbonates or hydroxides, with suitable counterions.
  • An example of a specific buffer system is a mixture of ammonia and ammonium chloride.
  • the aerosol generating material having an agglomerated structure are formed from a precursor composition comprising active particles.
  • the precursor composition and/or the aerosol generating material does not include a binder or binding additive.
  • the precursor composition comprises a binder or binding additive.
  • the binding additive may be selected to assist in the formation of an agglomerated structure by helping to adhere the particles to each other and to other components in the composition.
  • Suitable binding additives include, for example, thermoreversible gelling agents such as gelatin, starches, polysaccharides, pectins, alginates, wood pulp, celluloses, and cellulose derivatives such as carboxymethylcellulose.
  • the precursor composition and/ or the aerosol generating material further comprises a diluent.
  • the diluent may be in solid or liquid form. In some embodiments, the diluent is inert or substantially inert.
  • the agglomerated structure formed from the precursor composition may have an increased surface area by including in the precursor composition particles of an inert filler material.
  • Suitable inert fillers maybe porous or non-porous.
  • the precursor composition and/or the aerosol generating material further comprises at least one aerosol forming agent which may be, for instance, a polyol aerosol generator or a non-polyol aerosol generator, preferably a non polyol aerosol generator. It may be a solid or liquid at room temperature, but preferably is a liquid at room temperature.
  • Suitable polyols include sorbitol, glycerol, and glycols like propylene glycol or triethylene glycol.
  • Suitable non-polyols include monohydric alcohols, high boiling point hydrocarbons, acids such as lactic acid, and esters such as diacetin, triacetin, triethyl citrate or isopropyl myristate.
  • a combination of aerosol forming agents may be used, in equal or differing proportions. Glycerol and propylene glycol may be particularly preferred.
  • the precursor composition and/ or aerosol generating material may include a flavour- modifier, to modify the flavour provided by the active particles or to add flavour.
  • the flavour-modifier may be included in the precursor composition. Alternatively or in addition, the flavour- modifier may be added to or applied to the agglomerated structure.
  • flavour and “flavourant” refer to materials which, where local regulations permit, may be used to create a desired taste, aroma or other somatosensorial sensation in a product for adult consumers. They may include naturally occurring flavour materials, botanicals, extracts of botanicals, synthetically obtained materials, or combinations thereof (e.g., tobacco, cannabis, licorice (liquorice), hydrangea, eugenol, Japanese white bark magnolia leaf, chamomile, fenugreek, clove, maple, matcha, menthol, Japanese mint, aniseed (anise), cinnamon, turmeric, Indian spices, Asian spices, herb, wintergreen, cherry, berry, red berry, cranberry, peach, apple, orange, mango, clementine, lemon, lime, tropical fruit, papaya, rhubarb, grape, durian, dragon fruit, cucumber, blueberry, mulberry, citrus fruits, Drambuie, bourbon, scotch,
  • the flavour may be imitation, synthetic or natural ingredients or blends thereof. They may be in any suitable form, for example, liquid such as an oil, solid such as a powder, or gas.
  • the flavour comprises menthol, spearmint and/ or peppermint.
  • the flavour comprises flavour components of cucumber, blueberry, citrus fruits and/or redberry.
  • the flavour comprises eugenol.
  • the flavour comprises flavour components extracted from tobacco.
  • the flavour comprises flavour components extracted from cannabis.
  • the flavour may comprise a sensate, which is intended to achieve a somatosensorial sensation which are usually chemically induced and perceived by the stimulation of the fifth cranial nerve (trigeminal nerve), in addition to or in place of aroma or taste nerves, and these may include agents providing heating, cooling, tingling, numbing effect.
  • a suitable heat effect agent may be, but is not limited to, vanillyl ethyl ether and a suitable cooling agent may be, but not limited to eucolyptol, WS-3.
  • the precursor composition and/ or the aerosol generating material further comprises a preservative.
  • Suitable preservatives would be readily known to the skilled person and would include, for example, those that are safe for use in products producing inhalable aerosols.
  • Examples of preservatives that might be used include: propylene glycol, carvacrol, thymol, L-menthol, 1,8-cineole, phenoxyethanol, PhytoCide, sorbic acid and its salts, sodium hydroxymethylglycinate, ethylhexylglycerin, parabens and vitamins such as vitamin E or vitamin C.
  • neither the precursor composition nor the aerosol generating material includes a gelling agent.
  • the aerosol generating material is in particulate form, being small, separate particles. In most embodiments, multiple particles will be incorporated into an apparatus in order to have the desired effect on the aerosol of the apparatus.
  • the particulate aerosol generating material has an average size (as measured by sieving) of from about 0.5 mm to about 4 mm. In some embodiments, it may be preferable for the granules to have an average size of from about 0.7 mm to about 3 mm.
  • the aerosol generating material is in monolithic form, being larger articles. In most embodiments, a single monolithic component will be incorporated into an apparatus in order to have the desired effect on the aerosol of the apparatus.
  • the monolithic components are roughly spherical or cylindrical in shape. They may have a diameter of from about 4 mm to about 10 mm. In some embodiments, the diameter may be from about 5 mm to about 8 mm. Cylindrical components may additionally have a length of from about 5 mm to about 80 mm, from about 15 mm to about 50 mm, or from about 20 mm to about 30 mm.
  • FIG. 1 is a flow chart showing the key steps in the processes of some embodiments of the present invention.
  • a tobacco starting material which may be pre-treated or pre- processed, is ground to the desired particle size.
  • the pH is optionally adjusted, either by adding one or more bases or by adding a buffer solution to the tobacco particles.
  • any additional components may be added to the precursor material. These additional components maybe in liquid form or is solid form. Additional solid components are preferably in particulate or powder form. The additional components may be added before, during or after the pH adjustment step. An agglomerated structure is then formed from the resultant precursor composition, by adhering the pH-adjusted tobacco particles and optional other components to form multi-particle entities.
  • water may be added to the precursor composition as a processing aid. For example, the presence of water may help to dissolve components of the precursor composition, such as the pH adjusting agent and sugars, and/or it may assist with binding or improve agglomeration.
  • the agglomerated structure maybe formed from the precursor composition by a process including one or more steps selected from the group consisting of granulation, extrusion and spheronisation.
  • a volatile component is added to the particles by infusion.
  • Granulation Granulation of the precursor composition involves the binding or fusing together of the particles of the precursor composition to form larger, multi-particle entities which are referred to herein as agglomerated structures.
  • the multi-particle entities formed by granulation are called granules and they may have various geometric shapes, including, for example, the general form of spheres, cylinders, and the like.
  • the granulation step used is wet granulation.
  • wet granulation granules are formed by the addition of a granulation liquid onto a powder bed. Agitation in the system, along with the wetting of the components within the precursor composition, results in the aggregation of the particles to produce wet granules.
  • the granulation liquid may be at least partially removed by drying to provide dry granules.
  • the granulation liquid may be water-based or solvent-based. Suitable granulation liquids include, for example, water, glycerol, ethanol and isopropanol, either alone or in combination.
  • the granulation liquid comprises an aerosol forming agent, such as glycerol or one of the other agents mentioned herein, and/ or a binder or binding agent. In some embodiments, no water is added to the precursor composition to aid granulation.
  • the granulation step used is dry granulation.
  • dry granulation granules are formed without using a granulation liquid. This type of process has the advantage that it does not expose the precursor composition to moisture and so there is no requirement to expose the granules to heat in order to dry them.
  • Forming granules by dry granulation involves compacting and densifying the precursor composition, usually under high pressure.
  • Extrusion of the precursor composition involves the feeding of the precursor composition through an orifice to produce an extruded agglomerate.
  • the process which applies pressure to the precursor composition combined with shear forces, results in agglomerated structures.
  • Extrusion may be performed using one of the main classes of extruders: screw, sieve and basket, roll, ram and pin barrel extruders.
  • a single screw or twin screw extruder maybe used.
  • Forming the aerosol generating material by extrusion has the advantage that this processing combines mixing, conditioning, homogenizing and moulding of the precursor composition.
  • the free-flowing precursor composition is exposed to elevated pressure and temperature and is forced though an orifice, such as a shaping nozzle or die, to form an extruded agglomerate.
  • the extruded agglomerate has a rod-like form and/ or it may be cut into segments of a desired length as it exits the orifice. A rod-like extruded agglomerate may subsequently be cut into segments of desired length.
  • the precursor composition is exposed to temperatures from about 40°C to about 150°C, or from about 8o°C to about 130°C, or from about 6o°C to about 95°C within the extruder. In some embodiments, including those using double extrusion, the precursor composition is exposed to temperatures from about 70°C to about 95°C within the extruder. In some embodiments, including those using single extrusion, the precursor composition is exposed to temperatures from about 6o°C to about 8o°C within the extruder.
  • the composition maybe exposed to pressures (immediately before the die or nozzle) ranging from about 2 bar to about too bar, or from about 5 bar to about 60 bar, depending on the design of the die or nozzle being used.
  • the aerosol generating material formed from the extruded agglomerate exhibit good heat transfer and mass transfer, which has a positive impact on the release of the active substance and the volatile component.
  • the extrusion may be a generally dry process, with the precursor composition being a dry or substantially dry material that includes active particles, as well as optionally other particulate materials including, for example, base, diluent, solid aerosol forming agents, solid flavour modifiers, etc.
  • liquids may be added to the precursor composition during the extrusion process.
  • water may be added to the precursor composition, for example as a processing aid to assist dissolution or solubilisation of components of the composition, or to aid binding or agglomeration.
  • a wetting agent may be added to the precursor composition.
  • the liquid volatile component may be added to the precursor composition as a liquid component. This maybe in addition to or instead of applying the liquid volatile component to the agglomerated structures once they have been formed (as shown in Figure 1).
  • the liquid added to the precursor composition may be an aerosol forming agent such as glycerol or others discussed herein.
  • the liquid When liquid is added to the precursor composition in this manner, the liquid is applied not only on the surface, but, as a result of the extruder pressure combined with the intensive mixing by high shear forces, the extruded agglomerate becomes impregnated with the liquid.
  • the liquid is an aerosol forming agent
  • this can result in a high availability of the aerosol forming agent in the agglomerated product to enhance evaporation and release of the active substance and other volatile components from the agglomerated structure.
  • This same integration or impregnation of the agglomerated structure can be achieved if the liquid volatile component is added to the precursor composition and is extruded with the other components such as the active particles.
  • the amount of aerosol forming agent incorporated into the aerosol generating material may be at least about 1% by weight, at least about 1.5% by weight, at least about 2% by weight, at least about 3% by weight, at least about 5%, at least about 10%, at least about 15% or at least about 20% by weight.
  • the amount of aerosol forming agent incorporated into the aerosol generating material may be up to about 30% by weight and even up to about 40% by weight.
  • High amounts of aerosol forming agent such as at least about 10% or at least about 20% by weight, may be advantageous where the aerosol generating material is to generate an aerosol in addition to releasing the active substance(s) and volatile components.
  • Smaller amounts of aerosol forming agent such as up to about 5% by weight, may be sufficient where the aerosol generating material’s primary function is to releasing the active substance(s) and volatile components carried by the material into an existing aerosol or air flow.
  • the extruded agglomerate will be shaped by the nozzle or die through which it is forced. In some embodiments, the extruded agglomerate is cut into pieces of desired length. The pieces formed in this way may be used as the aerosol generating material or they may undergo further processing.
  • the nozzle or die is shaped to provide a solid strand of extruded agglomerate.
  • the extruded agglomerate may have the form of a solid cylindrical rod.
  • the extruded agglomerate may have different cross- sectional shapes, including oval, polygonal (such as triangular, square, etc.), and stars.
  • the extruded composition is formed into a desired shape selected to enhance or promote the release of the active substance and volatile components, for example by providing a form having a large surface area per unit volume.
  • This large surface area maybe provided on the outer surface of the extruded agglomerate, for example by selecting cross-sectional shapes with large perimeter.
  • the large surface area may be provided through the creation of channels within the extruded agglomerate.
  • the nozzle is shaped to provide an extruded agglomerate with inner channels.
  • These inner channels provide further surface area and can enhance active substance and volatile component release.
  • Aerosol generating material formed from such shaped extruded agglomerate sections have an inner channel structure which have advantageous adjustable strand ventilation properties and a significantly enlarged inner surface leading to improved heat and mass transfer.
  • such shaped compositions exhibit better, more uniform release of active substance and flavour by evaporation.
  • the structure with inner channels exhibits significantly improved strength in both the radial and axial directions, which is beneficial for the further processing of the extruded agglomerate, for example when it is cut into segments.
  • extruded agglomerates with different physical properties may be prepared, including different heat transfer properties, draft resistance, and capable of producing different aerosols and/ or of modifying aerosols being drawn through the extruded agglomerate.
  • the extruded agglomerate is shaped upon discharge from the extruder.
  • the extruded agglomerate is cut to an initial length, for example l metre, and allowed to cool before then being cut into sections of the desired length to provide the nicotine delivery composition in the form of particles of the desired dimensions.
  • the extruded agglomerate maybe cooled just before or just as it leaves the extruder.
  • the cooling is intensive and involves exposing the extruded agglomerate, which will be at an elevated temperature, for example from about 30°C to about ioo°C, or from about 40°C to about 70°C, to a cooling means that will reduce the temperature to within a range of from about o°C to about 70°C, from about o°C to about 50°C, from about 5°C to about 25°C or from about 5°C to about 15°C.
  • This rapid cooling of the extruded agglomerate may enhance the internal and external stability of the extruded agglomerate.
  • it is the nozzle or die that is cooled to achieve this effect.
  • extrusion of the precursor composition includes reducing the temperature of the precursor composition before it reaches the nozzle or die.
  • Such cooling of the precursor composition may result in the formation of an extruded agglomerate with beneficial properties, or may improve the strand-shaping process, for example where channels are to be formed within the extruded agglomerate strand.
  • spheronisation is used to further process extruded segments.
  • These segments are typically cylindrically-shaped and are cut or broken into uniform lengths following extrusion. They are then gradually transformed into spherical shapes by spheronisation. This shaping occurs as a result of plastic deformation and spheronisation can lead to spherical agglomerated structures, often with a nearly uniform diameter.
  • a volatile component is added to the particles by infusion.
  • the volatile component is provided in a solid or liquid form.
  • the low vapour pressure and high volatility of the volatile component causes the volatile component to transfer from the solid or liquid and to be deposited on the surface of the particles.
  • the volatile component may reside within pores on and within the particles.
  • the process of infusion involves addition/inclusion of the volatile component (either in solid form and having a specified PSD, or in liquid form) into a sealed container containing particles of aerosol generating material.
  • the contents is retained in the sealed container for a specified period of time under a controlled environment.
  • the volatile component is menthol and solid particles of menthol are used for infusion.
  • Agglomerated structures formed from nicotine particles, such as tobacco particles are placed into a container with particles of menthol.
  • the container is sealed and maintained at a constant temperature and humidity for a predetermined period of time.
  • the menthol volatilises and is adsorbed within the pores of the agglomerate structure.
  • equilibrium will be reached and the amount of volatile component present in and on the agglomerated structures will remain constant. At this point, there is no value is further infusion of the agglomerated structures.
  • gentle heating may be beneficial.
  • a similar process may be carried out with alternative active substances and/or with alternative volatile components having the required volatility and vapour pressure and/ or with volatile components in liquid form.
  • the volatile component is used in liquid form, there may be some adsorption of the volatile component in liquid form, as well as infusion. Incorporation into an apparatus
  • One or more particles of the aerosol generating material may be incorporated into an aerosol provision system, such as an apparatus for heating aerosol generating material to volatilise at least one component of the aerosol generating material.
  • the aerosol generating material may comprise, consist essentially of, or consist of an aerosol generating material as described herein.
  • the aerosol generating material used in the aerosol provision system further comprises one or more other aerosol generating materials, such as tobacco material.
  • an aerosol provision system includes non-combustible aerosol provision systems that release compounds from an aerosol generating material without combusting the aerosol-generating material, such as tobacco heating products, and hybrid systems to generate aerosol using a combination of aerosol-generating materials.
  • a “non-combustible” aerosol provision system is one where a constituent aerosol-generating material of the aerosol provision system (or component thereof) is not combusted or burned in order to facilitate delivery of at least one substance to a user.
  • the delivery system is a non-combustible aerosol provision system, such as a powered non-combustible aerosol provision system.
  • the non-combustible aerosol provision system is an electronic cigarette, also known as a vaping device or electronic nicotine delivery system (END), although it is noted that the presence of nicotine in the aerosol generating material is not a requirement.
  • the non-combustible aerosol provision system is an aerosol-generating material heating system, also known as a heat-not-burn system. An example of such a system is a tobacco heating system.
  • the non-combustible aerosol provision system is a hybrid system to generate aerosol using a combination of aerosol-generating materials, one or a plurality of which may be heated.
  • Each of the aerosol-generating materials may be, for example, in the form of a solid, liquid or gel and may or may not contain nicotine.
  • the hybrid system comprises a liquid or gel aerosol-generating material and a solid aerosol-generating material.
  • the solid aerosol-generating material may comprise, for example, tobacco or a non tobacco product.
  • the non-combustible aerosol provision system may comprise a non combustible aerosol provision device and a consumable for use with the non combustible aerosol provision device.
  • the disclosure relates to consumables comprising aerosol- generating material and configured to be used with non-combustible aerosol provision devices. These consumables are sometimes referred to as articles throughout the disclosure.
  • the non-combustible aerosol provision system such as a non-combustible aerosol provision device thereof, may comprise a power source and a controller.
  • the power source may, for example, be an electric power source or an exothermic power source.
  • the exothermic power source comprises a carbon substrate which may be energised so as to distribute power in the form of heat to an aerosol-generating material or to a heat transfer material in proximity to the exothermic power source.
  • the non-combustible aerosol provision system may comprise an area for receiving the consumable, an aerosol generator, an aerosol generation area, a housing, a mouthpiece, a filter and/ or an aerosol-modifying agent.
  • the consumable for use with the non-combustible aerosol provision device may comprise aerosol-generating material, an aerosol-generating material storage area, an aerosol-generating material transfer component, an aerosol generator, an aerosol generation area, a housing, a wrapper, a filter, a mouthpiece, and/ or an aerosol-modifying agent.
  • the aerosol generating material maybe positioned within the apparatus or device so that the active substance and volatile components that are released become entrained in an aerosol generated by the apparatus or device upon use, modifying the properties of the aerosol. Additionally or alternatively, the aerosol generating material may itself generate an aerosol during use, said aerosol including the released active substance and volatile components.
  • one or more particles of aerosol generating material are included in an aerosol provision system to volatilise components of the aerosol generating by heating but not combusting the material (i.e., a tobacco heating product or so-called Heat-not-Burn product).
  • the aerosol generating material is heated to generate an aerosol.
  • one or more particles of aerosol generating material are to be heated by such products.
  • one or more particles of aerosol generating material may be incorporated into tobacco material to form the material to be heated.
  • the one or more particles of aerosol generating material may be dispersed within the tobacco material, such as cut tobacco or reconstituted tobacco, to contribute to the active substances and flavour imparted by the tobacco.
  • the tobacco included in the material to be heated by the aerosol generating material heating system consists or consists essentially of one or more particles of aerosol generating material.
  • the aerosol generating material maybe heated directly. Where there are multiple particles of aerosol generating material, these may be held in a container or cartridge. At least portions of the container or cartridge may be permeable to air, to allow air to flow over or through the particles of aerosol generating material.
  • FIG 3 shows a cross-sectional view of an example of a tobacco heating product for heating an aerosol generating material.
  • the apparatus 11 has a heating chamber 14 which in use contains the aerosol generating material to be heated and volatilised.
  • the aerosol generating material is in the form of a monolithic nicotine delivery composition 13.
  • the aerosol generating material could however be multiple particles of aerosol generating material held in the heating chamber or provided in a cartridge like the one illustrated in Figure 5.
  • the apparatus 11 of Figure 3 further has an electronics/power chamber 16 which may, for example, contain electrical control circuitry and/or a power source (not shown).
  • the electrical control circuitry may include a controller, such as a microprocessor arrangement, configured and arranged to control the heating of the aerosol generating material via a heating element (not shown).
  • the electrical control circuitry may in use receive a signal from for example a puff-actuated sensor which is sensitive to for example changes in pressure or changes in rate of air flow that occur upon initiation of a draw on the apparatus 11 by a user.
  • the electrical control circuitry can then operate so as to cause heating of the aerosol generating material “on demand”.
  • Various arrangements for a puff-actuated sensor are available, including for example a thermistor, an electro-mechanical device, a mechanical device, an optical device, an opto-mechanical device and a micro electro mechanical systems (MEMS) based sensor.
  • the apparatus may have a manually operable switch for a user to initiate a puff.
  • the heating chamber 14 is contained within the housing 12. There may be a support and/ or insulating means (not shown) positioned between the heating chamber 14 and the housing 12, for example to assist in heat-insulating the housing 12 from the heating chamber 14, so that the housing 12 does not become hot or at least too hot to touch during use.
  • the housing 12 includes an inlet 15 through which air is drawn into the apparatus.
  • the housing 12 also includes an outlet 17 at a mouthpiece 18 of the apparatus 11. Air is drawn into the apparatus 11 through the inlet 15, travels through the apparatus picking up the active substance and other volatile constituents released by the aerosol generating material 13, and the resulting aerosol generated by the apparatus 11 leaves the apparatus 11 through the outlet 19 and is inhaled by the user.
  • one or more particles of the aerosol generating material are included in a so-called hybrid product for heating aerosol generating material to volatilise at least one component of an aerosol generating material.
  • the aerosol generating material is heated to generate an aerosol, in addition to the heating of a liquid, such as a nicotine-containing liquid or a nicotine- free liquid, which is heated by a heat source to form an aerosol or vapour.
  • the aerosol or vapour formed from the liquid is drawn over or through the aerosol generating material, picking up the active substance(s) and other volatilised components.
  • the aerosol or vapour formed from the liquid is not drawn over or through the aerosol generating material.
  • the material to be heated comprises the aerosol generating material and tobacco material, such as cut tobacco.
  • tobacco material such as cut tobacco.
  • one or more particles of aerosol generating material maybe incorporated into tobacco.
  • the one or more particles of aerosol generating material may be dispersed within the tobacco material, such as cut tobacco or reconstituted tobacco, to contribute to the flavour and active substances provided by the tobacco.
  • the aerosol generating material of the hybrid system consists of the particle of aerosol generating material.
  • FIG 4 shows a cross-sectional view of an example of a hybrid product for heating an aerosol generating material and a liquid.
  • the apparatus 21 has a housing 22 containing a chamber 24 which in use contains the aerosol generating material to be heated and volatilised.
  • the aerosol generating material is in the form of a monolithic aerosol generating material 23.
  • the aerosol generating material could however be multiple particles of aerosol generating material held in the chamber or provided in a cartridge like the one illustrated in Figure 5.
  • the housing 22 also contains a liquid reservoir 25 containing a liquid 26 to be heated to form a vapour.
  • the apparatus 21 further has an electronics/power chamber 27 which may, for example, contain electrical control circuitry and/or a power source (not shown).
  • the electrical control circuitry may include a controller, such as a microprocessor arrangement, configured and arranged to control the heating of the aerosol generating material and of the liquid 26 via one or more heating elements (not shown).
  • the electrical control circuitry may allow the apparatus 21 to be puff-actuated, so as to cause heating of the aerosol generating material “on demand”.
  • the apparatus 22 may have a manually operable switch for a user to initiate a puff.
  • the housing 22 also includes an inlet 28 through which air is drawn into the apparatus.
  • the housing 22 also includes an outlet 29 at a mouthpiece 30 of the apparatus 21.
  • Air is drawn into the apparatus 21 through the inlet 28, travels through the apparatus picking up the vapour created by heating the liquid 26 in the liquid reservoir 25, and active substance(s) and volatile component released by the aerosol generating material 23, and the resulting aerosol generated by the apparatus 21 leaves the apparatus 21 through the outlet 29 and is inhaled by the user.
  • the hybrid device 21 shown schematically in Figure 4 represents just one possible configuration of such an apparatus.
  • the relative positions of the liquid reservoir 25 and the aerosol generating material chamber 24 can be changed, as can the path of the air flowing through the apparatus.
  • the liquid reservoir is positioned upstream of the aerosol generating material to be volatilised.
  • the liquid reservoir may be positioned downstream of the aerosol generating material to be volatilised.
  • the two sources of aerosol in the apparatus may be arranged side- by-side, etc.
  • the vapour produced by heating the liquid in the liquid reservoir flows over or through the aerosol generating material comprising or consisting of one or more aerosol generating material.
  • the elevated temperature of the vapour causes the active substance and volatile components to be released.
  • the aerosol generating material maybe separately heated by a heating means.
  • a hybrid device in which the vapour created by heating a liquid heats the aerosol generating material in order to volatilise at least one component of the aerosol generating material.
  • the liquid is a nicotine-free liquid.
  • the liquid contains nicotine.
  • the device does not include a separate means for heating the aerosol generating material.
  • the vapour produced by heating the liquid in the liquid reservoir does not flows over or through the aerosol generating material. Rather, this vapour and the aerosol generated by heating the aerosol generating material only mix after they are both formed.
  • the tobacco heating products and hybrid products described herein may, in some embodiments, include aerosol generating material in the form of containers or cartridges containing the aerosol generating material. These containers or cartridges may be removable. They may replace both the chamber holding the aerosol generating material and the aerosol generating material in the apparatus described above with reference to Figures 3 and 4, and in the alternative embodiments discussed.
  • a tobacco segment cartridge 31 comprising a housing 32 defining a cavity within which are held one or more particles of aerosol generating material (not shown).
  • the housing 32 may, for example be made from moulded plastic or the like.
  • ventilation holes 33 are provided in the housing 32 of the cartridge 31.
  • the cartridge 31 may further comprise heating means that is heatable by a suitable means in order to heat the one or more particles of aerosol generating material held therein.
  • menthol was used as the volatile component with which tobacco granules were infused to form a nicotine delivery composition.
  • Discrete menthol particles were used as the source of the volatile component.
  • the infusion step utilised the low vapour pressure of menthol to cause a transfer of menthol from the discrete menthol particles to pockets of menthol residing within the porous surface of the tobacco granules which are later released when the nicotine delivery composition is heated to generate an aerosol.
  • the process of infusion involved the addition of particles of menthol into a bag containing tobacco granules and left for a specified period of time under a controlled environment.
  • the performance of the mentholated infused granules was tested to assess the impact of the incorporation of the menthol in the composition when the granules were incorporated into a Hybrid device.
  • the extruded tobacco granules were formed from a feedstock comprising ground tobacco particles, sodium carbonate (Na 2 C0 3 ), carboxymethyl cellulose (CMC) and water.
  • the pH of the feedstock used was 8.5 for each of the samples produced.
  • the study used a range of menthol loading levels, as shown in the table below.
  • the nicotine delivery composition was incorporated into a Hybrid device, with 430 mg of the nicotine delivery composition included in the pod.
  • the liquid included in the device to form the aerosol for the purpose of this experiment was a proxy, non- flavoured liquid.
  • the figures show the average menthol delivery per puff over the course of 60 puffs. The data shows that the nicotine delivery composition provides a steady release of the volatile component, menthol.
  • the delivery system described herein can be implemented as a combustible aerosol provision system, a non-combustible aerosol provision system or an aerosol-free delivery system.

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Abstract

L'invention concerne un matériau de génération d'aérosol destiné à être inclus dans un système de fourniture d'aérosol, tel qu'un appareil pour chauffer un matériau de génération d'aérosol pour volatiliser au moins un composant de celui-ci, le matériau de génération d'aérosol comprenant une substance active et un composant volatil incorporé par infusion. L'invention concerne également des procédés pour la préparation de telles compositions et un appareil comprenant de tels matériaux.
EP21726696.4A 2020-05-05 2021-05-04 Matériau de génération d'aérosol Pending EP4146018A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GBGB2006645.2A GB202006645D0 (en) 2020-05-05 2020-05-05 Aerosol generating material
PCT/GB2021/051065 WO2021224603A1 (fr) 2020-05-05 2021-05-04 Matériau de génération d'aérosol

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EP4146018A1 true EP4146018A1 (fr) 2023-03-15

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US (1) US20230165298A1 (fr)
EP (1) EP4146018A1 (fr)
JP (1) JP2023523911A (fr)
KR (1) KR20230005379A (fr)
CA (1) CA3173500A1 (fr)
GB (1) GB202006645D0 (fr)
MX (1) MX2022013097A (fr)
WO (1) WO2021224603A1 (fr)

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GB202204807D0 (en) * 2022-04-01 2022-05-18 Nicoventures Trading Ltd A component comprising an aerosol-generating material and uses thereof
GB202303474D0 (en) * 2023-03-09 2023-04-26 British American Tobacco Investments Ltd Aerosol generating material
WO2024200568A1 (fr) * 2023-03-29 2024-10-03 Jt International Sa Procédé

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WO2021224603A1 (fr) 2021-11-11
KR20230005379A (ko) 2023-01-09
JP2023523911A (ja) 2023-06-08
US20230165298A1 (en) 2023-06-01
CA3173500A1 (fr) 2021-11-11
GB202006645D0 (en) 2020-06-17
MX2022013097A (es) 2023-01-04

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