Aerosol forming component

Information

  • Patent Grant
  • 10765147
  • Patent Number
    10,765,147
  • Date Filed
    Monday, April 27, 2015
    9 years ago
  • Date Issued
    Tuesday, September 8, 2020
    4 years ago
Abstract
An aerosol forming component for volatilizing a liquid in an aerosol delivery device is disclosed. The aerosol forming component includes a first aerosol-forming member configured to be heated up to a first operating temperature and thereafter to a second higher operating temperature, and a second aerosol-forming member configured to be heated up to at least the first operating temperature as the first aerosol-forming member reaches the second higher operating temperature so that liquid volatilized from the two aerosol-forming members mix with one another.
Description
CROSS-REFERENCE TO RELATED APPLICATIONS

The present application is a National Phase entry of PCT Application No. PCT/GB2015/051213, filed on 27 Apr. 2015, which claims priority to GB Patent Application No. 1407426.4, filed on 28 Apr. 2014, which are hereby fully incorporated herein by reference.


TECHNICAL FIELD

The disclosure relates to an aerosol forming component and an aerosol delivery device comprising such an aerosol forming component. The disclosure also relates to a method for volatilizing liquids from an aerosol delivery device.


BACKGROUND

The use of a heating component to effect volatilization of a liquid material from an aerosol delivery device for subsequent inhalation by a user is known. Such devices comprise a single heating element or a heating component composed of multiple heating elements which are activated simultaneously. However, the use of such heating elements has disadvantages.


Liquid material intended for use in an aerosol delivery device which comprises a heating element typically comprises several constituents having variable volatilities. As a result, when the heating element(s) is activated, the more volatile constituents vaporize before the less volatile constituents. This can result in asynchronous release of constituents from the aerosol delivery device, and deposition of the more volatile constituents in the aerosol delivery device, mouth cavity or throat of the user.


For example, nicotine-containing solution for use in an aerosol delivery device as an alternative to the use of a smoking article typically comprises water, which has a boiling point of 100° C.; nicotine, which has a boiling point of 247° C.; and glycerol, which has a boiling point of 290° C. Upon contact with an activated heating element, the water, being the most volatile, will vaporize first, followed by the nicotine, and then the glycerol. Depending on the composition of the liquid material at least a portion, most or all of the nicotine may be vaporized together with the water. This asynchronous release of substances results in a relatively high concentration of nicotine in the gas and particle phase of the generated condensation aerosol in an early stage of the inhalation, yet most of this nicotine will never reach the lungs of the user, but rather will be deposited in the aerosol delivery device, mouth cavity or throat of the user as a result of dissociation from the glycerol.


SUMMARY

According to an aspect of the present disclosure, there is provided an aerosol forming component for volatilizing a liquid in an aerosol delivery device, comprising a first aerosol-forming member configured to be heated up to a first operating temperature and thereafter to a second higher operating temperature, and a second aerosol-forming member configured to be heated up to at least the first operating temperature as the first aerosol-forming member reaches the second higher operating temperature so that liquid volatilized from the two aerosol-forming members mix with one another.


In one embodiment, the first aerosol-forming member may reach the second operating temperature substantially at the same time as the second aerosol-forming member reaches the first operating temperature such that liquid volatilized from the two aerosol-forming members mix with one another.


In one embodiment, the aerosol-forming members may be configured to have different heating rates, such that by activating the aerosol-forming members simultaneously, the first aerosol forming member reaches the second operating temperature substantially at the same time as the second aerosol-forming member reaches the first operating temperature.


In another embodiment, the first aerosol-forming member may be activated prior to activation of the second aerosol-forming member such that the first aerosol forming member reaches the second operating temperature substantially at the same time as the second aerosol-forming member reaches the first operating temperature.


In yet another embodiment, the first aerosol-forming member may be located upstream of the second aerosol-forming member with respect to the flow of air through the aerosol delivery device in use.


In an alternative embodiment, the first and second aerosol-forming members may be located next to each other in a direction transverse to the flow of air through the aerosol forming component in use.


In one embodiment, the aerosol forming component may further comprise a liquid for volatilization, wherein the liquid comprises one or more aerosol generating means and one or more low boiling point fraction(s).


The liquid may comprises nicotine and/or one or more volatile acids.


In one embodiment, the aerosol generating means are volatilized from the first aerosol-forming member as it reaches the second operating temperature and the one or more low boiling point fraction(s) are volatilized from the second aerosol-forming member when it reaches its first operating temperature such that the one or more low boiling point fraction(s) settles on the aerosol generating means.


According to another aspect, there is provided an aerosol delivery device comprising an aerosol forming component as described above.


The aerosol delivery device may comprise a housing comprising an air inlet and an air outlet, an aerosol chamber in fluid communication with the air inlet and the air outlet, and a power source to which the aerosol forming members are electrically connected and a controller for controlling activation of the aerosol-forming members.


According to yet another aspect of the invention there is provided a method for volatilizing a liquid within an aerosol delivery device comprising a first and a second aerosol-forming member, the method comprises heating up the first aerosol-forming member to a first operating temperature and thereafter to a second higher operating temperature, and heating up the second aerosol-forming member to at least the first operating temperature as the first aerosol-forming member reaches the second higher operating temperature so that liquid volatilized from the aerosol-forming members mix with one another.


The method may further comprise heating up the first aerosol-forming member to a first operating temperature and thereafter to a second higher operating temperature, and heating up the second aerosol-forming member so that it reaches the first operating temperature substantially at the same time as the first aerosol-forming member reaches its second operating temperature.


In one embodiment, the aerosol-forming members are configured to have different heating rates, and the method comprises activating the aerosol-forming members simultaneously and the first aerosol forming member reaches the second operating temperature substantially at the same time as the second aerosol-forming member reaches the first operating temperature.


In another embodiment, the first aerosol-forming member is activated prior to activation of the second aerosol-forming member such that the first aerosol forming member reaches the second operating temperature substantially at the same time as the second aerosol-forming member reaches the first operating temperature.





BRIEF DESCRIPTION OF THE DRAWINGS

Embodiments of the disclosure will now be described, by way of example only, with reference to the accompanying drawings, in which:



FIG. 1A shows a front view of an aerosol delivery device according to the disclosure.



FIG. 1B shows a side view of the aerosol delivery devices.



FIG. 1C shows a top view of the aerosol delivery device.



FIG. 2 show a cross-sectional side view of an aerosol delivery device component according to the disclosure.



FIG. 3 shows a cross-sectional view of the aerosol delivery device component transverse to the plane of view of FIG. 2.



FIG. 4 shows a front planar view of the aerosol delivery device component partially without a housing.





DETAILED DESCRIPTION

The term “aerosol generating means” as used herein means a substance which rapidly creates or promotes an aerosol upon reaching volatilization temperature.


The term “capillary structure” as used herein refers to any structure through which liquid can travel as a result of capillary action.


The term “upstream” as used herein is with reference to the flow of air and aerosol through the aerosol delivery device in use.


The term “activated” as used herein with regard to an aerosol-forming member means the initiation of supply of an electric current to the aerosol-forming member so that it heats up to an operating temperature.


The term “operating temperature” as used herein means a temperature at which at least one of the constituents of a liquid material is volatilized upon contact with, or being placed in close proximity to the activated aerosol-forming member.


The term “sequentially” as used herein is with reference to the supply of electrical energy from an energy store to the aerosol-forming members in a serial fashion, so that the first aerosol-forming member (i.e. the aerosol-forming member located most upstream with respect to the flow of air through the aerosol delivery device in use) is activated first; followed by activation of the second aerosol-forming member, which is located downstream of the first member; followed by activation of the third aerosol forming member, which is located downstream of the second member, etc.


The term “aerosol delivery device” as used herein refers to a device capable of generating and delivering aerosol to a user.


The term “capillary gap” as used herein is considered to be any gap that brings about a liquid transport by virtue of the capillary action of its boundary walls.


Referring now to FIGS. 1A, 1B and 1C, an embodiment of an aerosol delivery device 1 according to the invention is shown from different views. The size and form of such aerosol delivery device 1 may be configured so that they can be easily and conveniently handled by the user, for example, the aerosol delivery device 1 may have a volume of around 10-50 cm3.


The aerosol delivery device 1 may be of any design which is suitable for creation and delivery of vaporized liquid material.


As shown in FIGS. 1A to 1C, the aerosol delivery device 1 comprises an aerosol delivery device component 2 with a mouthpiece 3, an energy store component 4 having a power source and a controller (not shown) connected to an electrical circuit (not shown). The aerosol delivery device component 2 is shown in more detail in FIG. 2 and it is configured to be detachably attached to the energy store component 4 by the use of a snap-in hook 2a for insertion into a corresponding lug on the energy store component (not shown). However, it should be understood that any means of achieving this may be used, for example a snap connector comprising one or more snap-in hooks and corresponding latching lugs, or a tongue and groove arrangement.


The power source of the energy store component 4 may be a cylindrical lithium ion cell of size 18650 with a storage capacity of 1650 mAh and a current load of up to 30 A. Any power source which is suitable for activating aerosol-forming members located in the aerosol delivery device component 2 and effecting volatilization of the liquid material may be used, such as one or more batteries. Furthermore, aerosol delivery devices of smaller size may use flat lithium polymer pouch cells.


The controller of the energy store component 4 controls the flow of electric current from the power source to the aerosol delivery device component 2 as described below.


The aerosol delivery device component 2 comprises a housing 5 as seen in FIG. 2. A space inside the housing is divided by a partitioning wall 6 into an aerosol chamber 7 and a liquid reservoir 8. The liquid reservoir 8 contains a liquid material 8a, and an air cushion 9. In FIG. 2 the liquid reservoir 8 has a capacity of around 4 cm3, and the liquid charge is around 3.6 mls, however it should be understood that the present disclosure is not limited to these parameters.


The liquid material may comprise one or more stimulants, such as nicotine or one or more therapeutics. The stimulant or therapeutic may be included in the liquid material in the amount of 0.1-5%; 0.5-2%; 0.5-5%; 0.8-3%; or 1-2% by weight.


The liquid material may additionally comprise one or more aerosol generating means, such as polyhydric alcohols, glycerol, propylene glycol, triethylene glycol, triethyl citrate or high boiling point hydrocarbons. The aerosol generating means may be included in the liquid material in the amount of 5-95%, 5-15%; 6-12%; 8-10% or around 10% by weight.


The liquid material may additionally comprise one or more low boiling point fractions, such as water or ethanol. Such fractions can reduce viscosity of the liquid material, and may comprise 5-95% or more than 50%, 60%, 70%, 80%, 82% or 84% by weight of the liquid material in total.


The liquid material may comprise one or more additional constituents, such as lactic acid, succinic acid, levulinic acid, benzoic acid, phenyl acetic acid, acetic acid, formic acid. When the liquid material comprises nicotine, such an acid may be added to protonate the nicotine.


The liquid material may further comprise one or more flavorants. As used herein, the terms “flavor” and “flavorant” refer to materials which, where local regulations permit, may be used to create a desired taste or aroma in a product for adult consumers. In some embodiments, the flavor or flavorant may be menthol, citrus, vanillin, aniseed, transanethole, benzaldehyde or acetylaldehyde.


Referring again to FIG. 2, an inlet passage created by a tubular structure 10 fluidly communicates with the aerosol chamber 7 via a nozzle 20, and the other side of the aerosol chamber 7 fluidly communicates with an outlet aperture 3a formed in the mouthpiece 3. The inlet passage is ideally located at the opposite end of the aerosol delivery device 1 to the mouthpiece 3, as this prevents entry of rainwater in use. The inlet passage may comprise a flow restrictor 10a such as a fiber composite (such as that provided by Filtrona Fibertec GmbH) similar to that found in the filter of a cigarette, which imparts to the user a feeling similar to that of a drawing on a cigarette upon inhalation through the aerosol delivery device.


An aerosol forming component is located in the aerosol chamber 7. The aerosol forming component comprises at least two aerosol-forming members. In FIG. 2, the aerosol forming component is composed of five aerosol-forming members, 11A-11E. The nozzle 20 directs air inhaled by the user via the inlet passage pass or across the five aerosol-forming members 11A-11E.


The aerosol-forming members 11A-11E may be of any design which is suitable for effecting vaporization of the liquid material 8a in an aerosol delivery device upon application of electrical input.


The aerosol forming-members 11A-11E may also be any shape suitable for purpose, and may be shaped so as to increase the surface area available for volatizing or evaporating the liquid material 8a. In one embodiment, the aerosol-forming members 11A-11E may comprise a sheet of material having a single layer that is configured to wick and heat the liquid material 8a. Thus, the sheet of material can absorb liquid material from the solution reservoir 8 and thereafter heat it up so that it vaporizes or evaporates and forms a vapor. The sheet of material is sheet-like in nature and may have a rectangular shape. However, it should be understood that the sheet of material may be of any shape, for example, circular, oval or square. The sheet of material comprises two opposing major surfaces. The sheet of material may comprise an open-pored structure, foam structure or interconnecting network of pores, all of which form a capillary structure.


The aerosol-forming members 11A-11E may be made of a homogenous, granular, fibrous or flocculent sintered metal(s) so as to form said capillary structure. In another embodiment, the aerosol-forming members 11A-11E comprise an open-pored metallic foam which also forms a capillary structure. Alternatively, the aerosol-forming members 11A-11E may be formed from a mesh material providing a capillary structure. The aerosol-forming members 11A-11E may be made of stainless steel such as AISI 304 or AISA 316 or heat conducting alloys such as NiCr alloys. The capillary structure is exposed at least on one of the major surfaces of each aerosol-forming member 11A-11E. For example, the aerosol-forming members 11A-11E may be formed with a capillary structure that extends completely throughout the aerosol-forming members 11A-11E such that it is exposed on both major surfaces of the sheet of material of each aerosol-forming member 11A-11E. In another embodiment, the aerosol-forming members 11A-11E are configured such that the capillary structure does not extend completely throughout each of the aerosol-forming members 11A-11E. For example, the capillary structure may only be exposed on one of the major surfaces or a section of both or either of the major surfaces of each aerosol-forming member 11A-11E.


The material from which the aerosol-forming members 11A-11E are formed is heatable in that it comprises sufficient electrical resistivity so that when an electric current is passed through, the aerosol-forming member heats up to a temperature sufficient to cause the liquid material 8a held in the capillary structure to evaporate or vaporize. In the embodiments wherein the sheet of material of each aerosol-forming member 11A-11E comprises a single layer as described above, the aerosol-forming members 11A-11E can be considered to comprise a heating element formed with a capillary structure such that the heating element and the capillary structure are integrated and form a single entity or unit.


In the above described embodiments wherein the sheet of material of each aerosol-forming member 11A-11E comprises a single layer configured to wick and heat a solution, the sheet of material can be described as comprising a heating element and a wick that are arranged in the same surface.


In an alternative un-illustrated embodiment, the aerosol-forming members comprise a sheet of material that is sheet-like in nature and formed from a plurality of layers. For example, each aerosol-forming member may comprise a first heatable layer acting as a heating element. This first layer is formed from a material that is configured to be heated up. Each aerosol-forming member may further comprise a second layer formed with an open-pored structure, foam structure, mesh structure, or interconnecting network of pores, all of which form a capillary structure. The capillary structure enables each aerosol-forming member to wick or absorb a liquid material. This second layer may be made of a homogenous, granular, fibrous or flocculent sintered metal(s) all of which form said capillary structure. The aerosol-forming members may be made of stainless steel, oxidized metals, glass, ceramic, carbon and/or cotton. In all these embodiments, the second layer acts as a wick.


The first layer (heating element) and the second layer (wick having a capillary structure) of each aerosol-forming member are laid on top of each other so as to form a sheet of material having two opposing major surfaces, wherein the capillary structure is exposed on one of the major surfaces.


In an alternative un-illustrated embodiment, the sheet of material of each aerosol-forming member comprises a third layer that is similar to the second layer in that it comprises a capillary structure. The second and the third layers of each aerosol-forming member sandwich the first layer such that the capillary structure is exposed on both major surfaces of the sheet of material of each aerosol-forming member.


In the embodiments wherein the sheet of material of each aerosol-forming member is formed from a plurality of layers as described above, the first layer acting as the heating element and the second and/or third layer(s) acting as the wick are parallel and connected to each other. The layers may be connected to each other by mechanical or chemical means. In one embodiment, the layers are sintered to one another.


The sheet of material of each aerosol-forming member according to any of the above described embodiments has thickness or depth that falls within the range of 20-500 μm. Alternatively, the thickness falls within the range of 50 to 200 μm. The thickness or depth should be understood as meaning the distance between the major surfaces of the sheet of material.


The opposing free ends of each aerosol forming member 11A-11E is mounted onto, or in connection with, a support plate 12, and arranged so that the aerosol forming members 11A-11E extend into the aerosol chamber 7 as can be seen in FIG. 2. Thus, a major portion of each aerosol-forming member 11A-11E is suspended in the aerosol chamber 7. The support plate 12 may be a printed circuit board electrically connecting each aerosol-forming member to the battery in the energy store component 4 so that each aerosol-forming member 11A-11E can be selectively activated. This is achieved by an end portion of the support plate 12 forming electrical connectors 17 which are configured to slot into a corresponding electrical socket (not shown) of the energy store component 4. As can be seen in FIG. 4, the aerosol delivery device component 2 comprise six electrical connectors 17, one of which is an earth, with the remaining five connectors being capable of each activating one of the five aerosol-forming members 11A-11E. The electrical socket (not shown) of the energy store component 4 is electrically connected to the battery (not shown).



FIG. 3 shows a cross-sectional view of the aerosol delivery device component 2 according to the invention. As can be appreciated from FIG. 3, the aerosol forming members 11A-11E are curved or bent such that they have an omega-shaped (Ω-shaped) cross-section. Each aerosol forming member 11A-E has opposing ends, 23a and 23b. The opposing ends 23a and 23b are mounted to the support plate 12 so that the aerosol forming members 11A-11E extend into the aerosol chamber 7. The ends 23a, 23b are sandwiched between the support plate 12 and the partitioning wall 6, thereby creating gaps between the support plate 12 and the partitioning wall 6 proximate to the ends 23a and 23b of each aerosol-forming member. These gaps have sufficient width so as to provide a capillary effect, and thus are referred to as capillary gaps 16. Supply apertures 13 are formed in the partitioning wall 6 such that the liquid reservoir 8 and capillary gaps 16 are in fluid communication.


Operation of the aerosol delivery device will now be described with reference to the drawings in FIGS. 1 to 4.


The coupling of the aerosol delivery device component 2 to the energy store component 4 by the user is registered by the controller (not shown), which may result in certain preparatory operations, such as activating one or more of the aerosol-forming members 11A-11E with the object of supplying them with fresh liquid material. Once completed, the controller may be configured to operate a light emitting diode (not shown) so as to indicate to the user that the aerosol delivery device 1 is ready for use.


The aerosol delivery device 1 may then be activated as a result of the user inhaling through the device. This can be achieved by a pressure sensor or flow sensor located in the air passage of the aerosol delivery device 1. Alternatively, the user may activate the aerosol delivery device 1 manually, by depressing a button or other activation mechanism (not shown) on the aerosol delivery device 1.


In either case, activation of the aerosol delivery device 1 results in the controller activating the aerosol forming members 11A-11E in a differential fashion by operating the battery so that it supplies an electric current to the aerosol-forming members 11A-11E via the printed circuit board. As the controller activates each aerosol-forming member 11A-11E an electric current flows through the selected aerosol-forming members such that they each increase in temperature. The controller may operate a transistor located in the energy store component 4 so as to control the flow of electric current to the aerosol-forming members 11A-11E.


Each aerosol forming member is heated for a period of time during activation, the duration of which depends upon the specifications of the aerosol forming members, and on the quantity and composition of the liquid material to be vaporized. In some embodiments, the heating period is between 1 and 1.8 seconds, less than 1 second, less than 0.8 second or less than 0.5 second.


The operating temperature of the aerosol-forming members 11A-11E will depend upon the composition of the liquid material 8a to be vaporized, or more specifically, upon the boiling points of the constituents of the liquid material 8a. It is also envisaged that the operating temperature may rise stepwise during the heating period when the constituents of the liquid material 8a has different boiling points. For example, if the liquid material comprises water, nicotine and glycerol, the aerosol delivery device 1 may be configured such that the operating temperature may rise from ambient temperature to a first operating temperature of approximately 100-140° C., and thereafter the operating temperature may rise to a second operating temperature of approximately 290-330° C.


In one embodiment, the aerosol delivery device 1 is configured such that the aerosol-forming members 11A-11E are deactivated, i.e. the controller stops the battery from supplying an electric current to the aerosol-forming members, before all liquid material 8a held in the capillary structure of each aerosol-forming member have been vaporized so as to avoid their capillary structure from drying out which could result in a temperature runaway and overheating of the aerosol-forming members.


It is envisaged that the aerosol delivery device may be configured such that the operating temperature(s) differs from one inhalation or puff to another. This configuration is suitable if the composition of the liquid material changes from one inhalation or puff to another. The composition of the liquid material 8a may change from one inhalation or puff to another due to localized vaporization effects occurring during refill of liquid material into the capillary structure after the aerosol-forming members have been activated. These vaporization effects cause the aerosol-forming members to cool down quickly as heat is consumed to vaporize the liquid material 8a.


The electric current is supplied from the battery to each aerosol forming member, in a serial fashion, wherein the first (most upstream) aerosol forming member 11E is activated, followed by activation of the second aerosol forming member 11D (i.e. the aerosol forming member located immediately downstream to the first aerosol forming member), etc. This configuration enables less volatile constituents, for example aerosol generating means such as glycerol which has a relatively high boiling point, vaporized by the first aerosol-forming member 11E to interact with more volatile constituents, for example water or nicotine having a lower boiling point, vaporized by the second aerosol-forming member 11D as will now be described in more detail.


The first aerosol-forming member 11E is activated such that its temperature increases to a first operating temperature causing the more volatile constituents to vaporize from the capillary structure of the first aerosol-forming member 11E. Thereafter, the temperature of the first aerosol-forming member 11E is increased to a higher second operating temperature such that aerosol generating means which is less volatile than the other constituents of the liquid material 8a is vaporized. When the vaporized aerosol generating means has vaporized it mixes with ambient air drawn in by the user into the aerosol chamber 7, and condenses so as to form an aerosol. The formed aerosol travels across the second aerosol-forming member 11D due to the air flow generated by the user inhaling. The second aerosol-forming member 11D is activated after the first aerosol-forming member 11D such that the temperature of the second aerosol-forming member 11D increases to the first operating temperature substantially at the same time as the first aerosol-forming member 11E reaches its second operating temperature. This has the effect that the aerosol formed by the first aerosol-forming member 11E passes over the second aerosol-forming member 11D as the more volatile constituents are being vaporized or has just been vaporized from the second aerosol-forming member 11D. The vapor of the more volatile constituents of the second aerosol-forming member 11D is directed towards the aerosol formed from the first aerosol-forming member 11E causing the vapor of the more volatile constituents to condense onto the aerosol formed by the first aerosol-forming member 11E. The remaining aerosol-forming members 11C, 11B, 11A are activated in a serial or sequential fashion respectively so as to achieve the same effect. Advantageously, the amount of more volatile constituents condensing on structural walls and internal constituents of the aerosol delivery device is reduced compared those aerosol delivery devices known from the prior art.


An example will now be described of the above configuration wherein the liquid material comprises water, nicotine and glycerol. The first aerosol-forming member 11E is activated and heated up passed a first operating temperature of 100-140° C. towards a second operating temperature close to the boiling point of glycerol, 290-330° C. so that all constituents of the liquid material vaporize. As glycerol has a higher boiling point than nicotine and water, it will vaporize last. The vapor of glycerol condenses as it cools down and mixes with ambient air drawn in by the user into the aerosol chamber 7 so as to form aerosol glycerol particles. The aerosol glycerol particles then travel with the air flow generated by the user inhaling.


The second aerosol-forming member 11D is activated after the first aerosol-forming member 11E such that it is heated up to the first operating temperature close to the boiling point of water and nicotine 100-140° C. The second aerosol-forming member 11D is activated after the first aerosol-forming member 11E such that the temperature of the second aerosol-forming member 11D increases to the first operating temperature substantially at the same time as the first aerosol-forming member 11E reaches its second operating temperature. Thus, water and nicotine vaporize from the second aerosol-forming member 11D as aerosol glycerol particles from the first aerosol-forming member 11E passes over the second aerosol-forming member 11D. This causes the vapor of water and nicotine from the second aerosol-forming member 11D to condense onto the aerosol glycerol particles vaporized from the first aerosol-forming member 11E. After most of the water and nicotine have been vaporized from the second aerosol-forming member 11D it is heated up further to the second operating temperature close to the boiling point of glycerol, 290-330° C., so that glycerol vaporizes and thereafter condenses so as to form aerosol glycerol particles. The aerosol glycerol particles of the second aerosol-forming member 11D mixes with the aerosol glycerol particles of the first aerosol-forming member 11E as the user inhales so as to form a relatively enriched air flow of aerosol glycerol particles. The air flow enriched with aerosol glycerol particles travels towards the third aerosol-forming member 11C as the user inhales.


The third aerosol-forming member 11C is activated after the second aerosol-forming member 11D to the first operating temperature close to the boiling point of water and nicotine 100-140° C. The third aerosol-forming member 11C is activated after the second aerosol-forming member 11D such that the temperature of the third aerosol-forming member 11C increases to the first operating temperature substantially at the same time as the second aerosol-forming member 11D reaches its second operating temperature. Thus, water and nicotine vaporize from the third aerosol-forming member 11C as aerosol glycerol particles from the first and second aerosol-forming member 11E, 11D pass over the third aerosol-forming member 11C. This causes the vapor of water and nicotine from the third aerosol-forming member 11C to condense onto the aerosol glycerol particles of the first and second aerosol-forming member 11E, 11D. The third aerosol-forming member 11C is then heated up to the second operating temperature and the remaining aerosol-forming members 11B and 11A are activated thereafter in a similar serial fashion.


The aerosol formed by the aerosol forming component as described above is then drawn through a cooler 14, see FIG. 2, as the user continues to inhale so as to cool down the aerosol and to reduce the vapor pressure of the aerosol vapor phase. The cooler 14 can comprise a pore body which is substantially permeable to particles of the aerosol formed. Suitable materials include porous wadding, fleece-like synthetic material (such as Viledon® Filtermatten) synthetic non-wovens manufactured from polyolefin or polyester fibers, or an open-cellular foam material. The pore body may also comprise a regenerator material. Suitable materials have a relatively large surface or heat exchange surface which is capable of absorbing a large amount of heat rapidly without substantial flow losses. Examples include metal wool, metal chips, metal mesh, wire knits, open cell metal foams and fills made from metallic or ceramic granular material such as aluminum granules. Fills of activated charcoal granules could be used as an alternative. Thereafter, the aerosol passes through an absorber 15. The absorber may comprise an open-pore structure which may be similar to the cooler 14. The absorber 15 is intended to absorb condensate deposits from the vapor phase. The absorber material may comprise one or more absorbents such as citric acid which is binding the nicotine.


Flavorings such as menthol may be added to the cooler 14 and/or absorber 15. The cooler 14 and the absorber 15 are configured to refine the aerosol formed by the aerosol generating component to an extent that makes the aerosol more enjoyable to the user.


Finally, the aerosol is drawn into the mouth of the user.


After one inhalation or puff, the controller may prevent the aerosol forming component from being immediately activated so as to allow the aerosol forming members 11A-11E to cool down and replenish the aerosol forming members with liquid material 8a. This period may last for a few seconds, and may be indicated to the user by, for example, a light emitting diode.


Providing an aerosol forming component composed of two or more aerosol forming members wherein the aerosol-forming member most upstream member is activated prior to the second (and any subsequent) aerosol-forming member, improves aerosol formation process as a larger amount of more volatile constituents such as nicotine is carried by the aerosol particles. Differential activation of the aerosol forming members 11A-11E creates a temperature gradient along the aerosol forming component, akin to the temperature gradient that inherently occurs between the distillation zone and burning tip of a smoking article. This results in improved volatilization of the liquid material, and as a result, less volatile constituents of the material are vaporized approximately synchronously with the more volatile constituents. This has the benefit of avoiding or reducing condensation, and therefore deposition, of the more volatile constituents in the aerosol delivery device, mouth cavity or throat of the user.


It should be understood that the present disclosure is not limited to the aerosol forming component comprising a plurality of aerosol-forming members activated sequentially.


In another un-illustrated embodiment, the aerosol-forming members are configured to be activated simultaneously. In such an embodiment the aerosol-forming members are configured to have different heating rates. This may be achieved by forming the aerosol-forming members out of different materials. The aerosol-forming member most upstream is then configured to have the highest heating rate and the heating rate of each aerosol-forming member decreases in a downstream direction. When activating all aerosol-forming members simultaneously, the aerosol-forming members reach the first operating temperature in a serial fashion and the second operating temperature in a serial fashion in a direction of the airflow due to the decrease in heating rates. This has a similar effect to that described with reference to FIGS. 1A to 4 in that when activating all aerosol-forming members simultaneously a first aerosol-forming member is heated up to a first operating temperature and thereafter to a second higher operating temperature, and a second aerosol-forming member located downstream from the first aerosol-forming member with respect to the airflow is heated up to the first operating temperature at substantially the same time as the first aerosol-forming member reaches the second operating temperature so that liquid volatilized from the aerosol-forming members mix with one another.


Although in the embodiments described above the aerosol-forming members are located one after another in the direction of the airflow such that one is more upstream than another, the present disclosure is not limited to such an arrangement. For example, in an un-illustrated embodiment, the aerosol forming component comprise a plurality of aerosol-forming members located next to each other in a direction transverse to the air flow, in other words one aerosol-forming member is not upstream or downstream relative to another aerosol-forming member. In such an embodiment, at least one of the aerosol-forming members is configured to be activated prior to another aerosol-forming member such that the at least one aerosol-forming member reaches the second operating temperature substantially at the same time as the other aerosol-forming member reaches the first operating temperature so that liquid volatilized from the aerosol-forming members mix with one another.


In yet another alternative un-illustrated embodiment, the aerosol forming component comprise a plurality of aerosol-forming members that are located next to each other in a direction transverse to the air flow. The aerosol-forming members are configured to comprise different heating rates such that when activating the aerosol-forming members simultaneously one aerosol-forming member reaches the second operating temperature substantially at the same time as another aerosol-forming member reaches the first operating temperature so that liquid volatilized from the aerosol-forming members mix with one another.


It should be understood that the embodiments of the aerosol forming component according to the present disclosure improve the aerosol formation process as a larger amount of more volatile constituents such as nicotine is carried by the aerosol particles. The aerosol-forming members being heated to the operational temperatures at different time points creates a temperature gradient within the aerosol forming component, akin to the temperature gradient that inherently occurs between the distillation zone and burning tip of a smoking article. This results in improved volatilization of the liquid material, and as a result, less volatile constituents of the material are vaporized approximately synchronously with the more volatile constituents. This has the benefit of avoiding or reducing condensation, and therefore deposition, of the more volatile constituents in the aerosol delivery device, mouth cavity or throat of the user.


In the embodiments according to the present disclosure, one aerosol-forming member is described to reach a second operating temperature at substantially the same time as another aerosol-forming member reaches a first operating temperature. “Substantially at the same time” is to be understood as a period of time that allows for the liquid vaporized from one aerosol-forming member as it reaches the second temperature to mix with liquid vaporized from another aerosol-forming member as it reaches the first operating temperature. The period of time may be less than 1 second (s), 0.75 s, 0.5 s, 0.1 s, 75 ms or 50 ms.


It should also be understood that one aerosol-forming member reaches a second operating temperature at substantially the same time as another aerosol-forming member reaches a first operating temperature during a single puff, drag or inhalation by the user or during one activation cycle.


In order to address various issues and advance the art, the entirety of this disclosure shows by way of illustration various embodiments in which that which is claimed may be practiced and provide for superior aerosol forming components, aerosol delivery devices and methods of volatilizing a liquid within an aerosol delivery device. The advantages and features of the disclosure are of a representative sample of embodiments only, and are not exhaustive and/or exclusive. They are presented only to assist in understanding and teach the claimed features. It is to be understood that advantages, embodiments, examples, functions, features, structures, and/or other aspects of the disclosure are not to be considered limitations on the disclosure as defined by the claims or limitations on equivalents to the claims, and that other embodiments may be utilized and modifications may be made without departing from the scope and/or spirit of the disclosure. Various embodiments may suitably comprise, consist of, or consist essentially of, various combinations of the disclosed elements, components, features, parts, steps, means, etc. In addition, the disclosure includes other inventions not presently claimed, but which may be claimed in future.

Claims
  • 1. An aerosol forming component for volatilizing a liquid in an aerosol delivery device, comprising: a first aerosol-forming member controlled to be heated up to a first operating temperature and thereafter to a second higher operating temperature; anda second aerosol-forming member controlled separated from the first aerosol-forming member to be heated up to reach the first operating temperature substantially at the same time as the first aerosol-forming member reaches the second higher operating temperature so that liquid volatilized from the first aerosol-forming member mixes with liquid volatilized from the second aerosol-forming member, wherein the first aerosol-forming member is located upstream of the second aerosol-forming member with respect to a flow of air through the aerosol delivery device in use, wherein the first and second aerosol-forming members each comprise a heater element and a wick, and wherein the heater element and the wick of each of the first and second aerosol-forming members are arranged in a common surface; further comprising: a housing comprising an air inlet and an air outlet; an aerosol chamber in fluid communication with the air inlet and the air outlet; a power source to which the first and second aerosol forming members are electrically connected; and a controller for controlling activation of the first and second aerosol-forming members.
  • 2. The aerosol forming component according to claim 1, wherein the first and second aerosol-forming members are configured to have different heating rates, such that by activating the first and second aerosol-forming members simultaneously, the first aerosol forming member reaches the second operating temperature substantially at the same time as the second aerosol-forming member reaches the first operating temperature.
  • 3. The aerosol forming component according to claim 1, wherein the first aerosol-forming member is activated prior to activation of the second aerosol-forming member such that the first aerosol forming member reaches the second operating temperature substantially at the same time as the second aerosol-forming member reaches the first operating temperature.
  • 4. The aerosol forming component according to claim 1, further comprising a liquid for volatilization, wherein the liquid comprises one or more substances which create or promote an aerosol upon reaching volatilization temperature.
  • 5. The aerosol forming component according to claim 1, wherein the liquid comprises nicotine.
  • 6. The aerosol forming component according to claim 4, wherein the liquid comprises one or more volatile acids.
  • 7. The aerosol forming component according to claim 4, wherein the aerosol generating means are volatilized from the first aerosol-forming member as the first aerosol-forming member reaches the second operating temperature and the one or more low boiling point fraction(s) are volatilized from the second aerosol-forming member when the second aerosol-forming member reaches the first operating temperature such that the one or more low boiling point fraction(s) settles on the aerosol generating means.
  • 8. An aerosol delivery device comprising an aerosol forming component according to claim 1.
Priority Claims (1)
Number Date Country Kind
1407426.4 Apr 2014 GB national
PCT Information
Filing Document Filing Date Country Kind
PCT/GB2015/051213 4/27/2015 WO 00
Publishing Document Publishing Date Country Kind
WO2015/166219 11/5/2015 WO A
US Referenced Citations (192)
Number Name Date Kind
2057353 Whittemore Oct 1936 A
2809634 Murai Oct 1957 A
3111396 Ball Nov 1963 A
3402724 Blount Sep 1968 A
3431393 Katsuda Mar 1969 A
3433632 Elbert Mar 1969 A
3521643 Toth Jul 1970 A
3604428 Moukaddem Sep 1971 A
3804100 Fariello Apr 1974 A
3964902 Fletcher Jun 1976 A
4009713 Simmons Mar 1977 A
4031906 Knapp Jun 1977 A
4094119 Sullivan Jun 1978 A
4145001 Weyenberg Mar 1979 A
4161283 Hyman Jul 1979 A
4193513 Bull Mar 1980 A
4503851 Brauroth Mar 1985 A
4588976 Jaselli May 1986 A
4676237 Wood Jun 1987 A
4677992 Bliznak Jul 1987 A
4735217 Gerth Apr 1988 A
4830028 Lawson May 1989 A
4848374 Chard Jul 1989 A
4885129 Leonard Dec 1989 A
4917301 Munteanu Apr 1990 A
4922901 Brooks May 1990 A
4947874 Brooks Aug 1990 A
4947875 Brooks Aug 1990 A
4978814 Honour Dec 1990 A
5027837 Clearman Jul 1991 A
5046514 Bolt Sep 1991 A
5060671 Counts Oct 1991 A
5095647 Zobele Mar 1992 A
5095921 Losee Mar 1992 A
5096921 Bollinger Mar 1992 A
5099861 Clearman et al. Mar 1992 A
5121881 Lembeck Jun 1992 A
5167242 Turner Dec 1992 A
5179966 Losee Jan 1993 A
5247947 Clearman Sep 1993 A
5269327 Counts Dec 1993 A
5322075 Deevi Jun 1994 A
5388574 Ingebrethsen Feb 1995 A
5390864 Alexander Feb 1995 A
5408574 Deevi Apr 1995 A
5479948 Counts Jan 1996 A
5497792 Prasad Mar 1996 A
5501236 Hill Mar 1996 A
5505214 Collins Apr 1996 A
5530225 Hajaligol Jun 1996 A
5540241 Kim Jul 1996 A
5553791 Alexander Sep 1996 A
5636787 Gowhari Jun 1997 A
5649554 Sprinkel Jul 1997 A
5659656 Das Aug 1997 A
5666977 Higgins Sep 1997 A
5692291 Seetharama Dec 1997 A
5743251 Howell et al. Apr 1998 A
5865185 Collins Feb 1999 A
5878752 Adams Mar 1999 A
6040560 Fleischhauer Mar 2000 A
6058711 Maciaszek May 2000 A
6095505 Miller Aug 2000 A
6155268 Takeuchi Dec 2000 A
6275650 Lambert Aug 2001 B1
6652804 Neuann Nov 2003 B1
6681998 Sharpe Jan 2004 B2
6701921 Sprinkel Mar 2004 B2
6790496 Levander Sep 2004 B1
7100618 Dominquez Sep 2006 B2
7112712 Ancell Sep 2006 B1
7263282 Meyer Aug 2007 B2
7400940 McRae Jul 2008 B2
7540286 Cross Jun 2009 B2
7767698 Warchol Aug 2010 B2
7832410 Hon Nov 2010 B2
7992554 Radomski Aug 2011 B2
8156944 Hon Apr 2012 B2
8365742 Hon Feb 2013 B2
8375957 Hon Feb 2013 B2
8393331 Hon Mar 2013 B2
8430106 Potter et al. Apr 2013 B2
8490628 Hon Jul 2013 B2
8511318 Hon Aug 2013 B2
8752545 Buchberger Jun 2014 B2
8689805 Hon Aug 2014 B2
8833364 Buchberger Sep 2014 B2
8910640 Sears Dec 2014 B2
8948578 Buchberger Feb 2015 B2
9609894 Abramov Apr 2017 B2
9623205 Buchberger Apr 2017 B2
10010695 Buchberger Jul 2018 B2
10045562 Buchberger Aug 2018 B2
20010042546 Umeda et al. Nov 2001 A1
20020005207 Wrenn Jan 2002 A1
20020016370 Shytle Feb 2002 A1
20020079309 Cox et al. Jun 2002 A1
20030005620 Shytle Jan 2003 A1
20030049025 Neumann Mar 2003 A1
20030079309 Cox Jun 2003 A1
20030106552 Sprinkel Jun 2003 A1
20030108342 Sherwood Jun 2003 A1
20030200964 Blakely Oct 2003 A1
20030202169 Liu Oct 2003 A1
20040031485 Rustad Feb 2004 A1
20040129793 Nguyen Jul 2004 A1
20040210151 Tsukashima Oct 2004 A1
20040226568 Takeuchi Nov 2004 A1
20050063686 Whittle Mar 2005 A1
20050145260 Inagaki Jul 2005 A1
20050194013 Wright Sep 2005 A1
20050204799 Koch Sep 2005 A1
20050268911 Cross Dec 2005 A1
20060078477 Althouse Apr 2006 A1
20060137681 Von Hollen Jun 2006 A1
20070014549 Demarest et al. Jan 2007 A1
20070045288 Nelson Mar 2007 A1
20070062548 Horstmann Mar 2007 A1
20070102013 Adams May 2007 A1
20070107879 Radomsnki May 2007 A1
20070155255 Galauner Jul 2007 A1
20070267031 Hon Nov 2007 A1
20080092912 Robinson et al. Apr 2008 A1
20080156326 Belcastro Jul 2008 A1
20080216828 Wensley Sep 2008 A1
20080241255 Rose Oct 2008 A1
20090090472 Radomski Apr 2009 A1
20090095311 Han Apr 2009 A1
20090188490 Han Jul 2009 A1
20090241947 Bedini Oct 2009 A1
20090272379 Thorens Nov 2009 A1
20090293892 Williams Dec 2009 A1
20100059070 Potter Mar 2010 A1
20100065653 Potter Mar 2010 A1
20100083959 Siller Apr 2010 A1
20100108059 Axelsson et al. May 2010 A1
20100236546 Yamada Sep 2010 A1
20100242974 Pan Sep 2010 A1
20110011396 Fang Jan 2011 A1
20110126848 Zuber Jun 2011 A1
20110155153 Thorens Jun 2011 A1
20110192914 Ishigami Aug 2011 A1
20110226236 Buchberger Sep 2011 A1
20110277757 Terry Nov 2011 A1
20110036363 Urtsev Dec 2011 A1
20110290267 Yamada Dec 2011 A1
20110297166 Takeuchi Dec 2011 A1
20110303231 Li Dec 2011 A1
20120145169 Wu Jun 2012 A1
20120260927 Liu Oct 2012 A1
20120285476 Hon Nov 2012 A1
20130074857 Buchberger Mar 2013 A1
20130081623 Buchberger Apr 2013 A1
20130087160 Gherge Apr 2013 A1
20130142782 Rahmel Jun 2013 A1
20130192615 Tucker Aug 2013 A1
20130213419 Tucker Aug 2013 A1
20130284192 Peleg Oct 2013 A1
20130333700 Buchberger Dec 2013 A1
20130340779 Liu Dec 2013 A1
20140000638 Sebastian Jan 2014 A1
20140060528 Liu Mar 2014 A1
20140060554 Collett Mar 2014 A1
20140060555 Chang Mar 2014 A1
20140182608 Egoyants Jul 2014 A1
20140202454 Buchberger Jul 2014 A1
20140202476 Egoyants Jul 2014 A1
20140209105 Sears Jul 2014 A1
20140216485 Egoyants Aug 2014 A1
20140238396 Buchberger Aug 2014 A1
20140238423 Tucker Aug 2014 A1
20140238424 Tucker Aug 2014 A1
20140261490 Kane Sep 2014 A1
20140270726 Egoyants Sep 2014 A1
20140270730 DePiano Sep 2014 A1
20140283825 Buchberger Sep 2014 A1
20140286630 Buchberger Sep 2014 A1
20140299125 Buchberger Oct 2014 A1
20140338680 Abramov Nov 2014 A1
20150114411 Buchberger Apr 2015 A1
20150157055 Lord Jun 2015 A1
20150181934 Lyubomirskiy Jul 2015 A1
20150196058 Lord Jul 2015 A1
20150208728 Lord Jul 2015 A1
20160073693 Reevell Mar 2016 A1
20160106154 Lord Apr 2016 A1
20160106155 Reevell Apr 2016 A1
20170006916 Qiuming Jan 2017 A1
20170042245 Buchberger Feb 2017 A1
20170197043 Buchberger Jul 2017 A1
20170197044 Buchberger Jul 2017 A1
20170197046 Buchberger Jul 2017 A1
Foreign Referenced Citations (134)
Number Date Country
508244 Dec 2010 AT
510405 Apr 2012 AT
510504 Apr 2012 AT
6391373 Jun 1975 AU
6393173 Jun 1975 AU
2309376 Nov 2000 CA
698603 Sep 2009 CH
2092880 Jan 1992 CN
2220168 Feb 1996 CN
1205849 Jan 1999 CN
2719043 Aug 2005 CN
1694765 Nov 2005 CN
201238609 May 2009 CN
201375023 Jan 2010 CN
101648041 Feb 2010 CN
101878958 Nov 2010 CN
202172846 Mar 2012 CN
102655773 Sep 2012 CN
202722498 Feb 2013 CN
202750708 Feb 2013 CN
105310114 Feb 2016 CN
106102863 Nov 2016 CN
1950439 Apr 1971 DE
3148335 Jul 1983 DE
3218760 Dec 1983 DE
3936687 May 1992 DE
29719509 Jan 1998 DE
19630619 Feb 1998 DE
19654945 Mar 1998 DE
10330681 Jun 2004 DE
202006013439 Oct 2006 DE
202013100606 Feb 2013 DE
019736 May 2014 EA
022685 Feb 2016 EA
280262 Aug 1988 EP
0358002 Mar 1990 EP
0358114 Mar 1990 EP
0444553 Sep 1991 EP
04888488 Jun 1992 EP
0845220 Jun 1998 EP
0295122 Dec 1998 EP
0893071 Jan 1999 EP
1166814 Jan 2002 EP
1166847 Jan 2002 EP
1736065 Dec 2006 EP
1757921 Feb 2007 EP
2018886 Jan 2009 EP
2022349 Feb 2009 EP
2113178 Nov 2009 EP
2340729 Jul 2011 EP
2698070 Feb 2014 EP
2907397 Apr 2014 EP
2762019 Aug 2014 EP
2835062 Feb 2015 EP
960469 Apr 1950 FR
25575 Mar 1912 GB
1313525 Apr 1973 GB
1196511 Dec 2014 HK
1226611 Oct 2017 HK
S57-052456 Mar 1982 JP
S59-106340 Jan 1986 JP
61-096765 May 1986 JP
S61-096763 May 1986 JP
2124081 May 1990 JP
H5-103836 Apr 1993 JP
H05-309136 Nov 1993 JP
H6-315366 Nov 1994 JP
H8-511176 Oct 1995 JP
H08-299862 Nov 1996 JP
11089551 Apr 1999 JP
2011518567 Jan 2002 JP
2004332069 Nov 2004 JP
2005-538159 Dec 2005 JP
2005537918 Dec 2005 JP
2009-509523 Mar 2009 JP
2009-537119 Oct 2009 JP
2012-249854 Dec 2012 JP
1020050037919 Apr 2006 KR
20130006714 Nov 2013 KR
2336001 Nov 2005 RU
2311859 Dec 2007 RU
89927 Dec 2009 RU
94815 Jun 2010 RU
103281 Apr 2011 RU
115629 May 2012 RU
122000 Nov 2012 RU
124120 Jan 2013 RU
132318 Sep 2013 RU
2509516 Mar 2014 RU
WO9527412 Oct 1995 WO
WO9632854 Oct 1996 WO
WO9748293 Dec 1997 WO
WO98017131 Apr 1998 WO
WO200009188 Feb 2000 WO
WO200021598 Apr 2000 WO
WO2000050111 Aug 2000 WO
WO2002051468 Jul 2002 WO
WO2002058747 Aug 2002 WO
WO2003028409 Apr 2003 WO
WO 2003050405 Jun 2003 WO
WO2003083283 Oct 2003 WO
WO 2003101454 Dec 2003 WO
WO2004022128 Mar 2004 WO
WO2004022242 Mar 2004 WO
WO2004022243 Mar 2004 WO
WO2005106350 Nov 2005 WO
WO2006082571 Aug 2006 WO
WO 2007042941 Apr 2007 WO
WO 2007131449 Nov 2007 WO
WO2007141668 Dec 2007 WO
WO2008038144 Apr 2008 WO
WO2009015410 Feb 2009 WO
WO2009118085 Oct 2009 WO
WO 2009132793 Nov 2009 WO
WO2010045670 Apr 2010 WO
WO2010045671 Apr 2010 WO
WO 2011050943 May 2011 WO
WO 2011109849 Sep 2011 WO
WO 2012025496 Mar 2012 WO
WO 2013034453 Mar 2013 WO
WO 2013034460 Mar 2013 WO
WO 2013057185 Apr 2013 WO
WO 2013082173 Jun 2013 WO
WO 2013098395 Jul 2013 WO
WO2013116558 Aug 2013 WO
WO2013116572 Aug 2013 WO
WO2014130695 Aug 2013 WO
WO2013152873 Oct 2013 WO
WO 2014012906 Jan 2014 WO
WO2014061477 Apr 2014 WO
WO 2014140320 Sep 2014 WO
WO 2014150131 Sep 2014 WO
WO 2015114328 Aug 2015 WO
WO 2015165812 Nov 2015 WO
Non-Patent Literature Citations (71)
Entry
International Search Report and Written Opinion dated Feb. 6, 2013 for PCT/EP0212/070647 filed Oct. 18, 2012.
Chinese Office Action for Chinese Application No. 201480024978.X dated Jan. 18, 2017.
European Search Report for European Application No. 15178588 dated Apr. 14, 2016.
International Preliminary Report on Patentability, dated Apr. 22, 2014, for International Patent Application No. PCT/EP2012/070647, filed Oct. 18, 2012.
International Search Report and Written Opinion for International Application No. PCT/EP2012/003103, dated Nov. 26, 2012.
International Search Report and Written Opinion for PCT/AT/2012/000017 dated Jul. 3, 2012.
International Search Report and Written Opinion for PCT/GB2014/051333 dated Jul. 17, 2014.
International Search Report and Written Opinion, International Application No. PCT/GB2014/051332 dated Jul. 21, 2014.
International Search Report and Written Opinion, International Application No. PCT/GB2014/051334 dated Jul. 21, 2014.
IPRP mailed Aug. 5, 2015 for International Application No. PCT/GB2014/051333.
IPRP, International Application No. PCT/GB2014/051332 mailed Nov. 12, 2015.
IPRP, International Application No. PCT/GB2014/051334 mailed Nov. 12, 2015.
Japanese Notice of Reasons for Rejection for Japanese Application No. 2015-137361 dated May 31, 2016.
Russian Search Report for Russian Application No. 2015146843/12 (072088) date completed Apr. 24, 2017.
Russian Office Action, Application No. 2014120213/12, dated Oct. 26, 2016, 7 pages.
Russian Office Action, Application No. 2014120213/12, dated Sep. 22, 2017, 11 pages.
Chinese Office Action, Application No. 201480024988.3, dated Dec. 30, 2016, 26 pages.
Chinese Office Action, Application No. 201480024988.3, dated Sep. 11, 2017, 21 pages.
European Extended Search Report, Application No. 17189951.1, dated Jan. 4, 2018, 8 pages (11 pages with translation).
Plasma polymerization (the company Diener electronic GmbH+Co. KG), www.plasma.de, retrieved on Oct. 17, 2017, 19 pages.
International Preliminary Report on Patentability (WIPO English Translation), dated Aug. 13, 2013 for International Patent Application No. PCT/AT2012/000017, filed Feb. 2, 2012.
Pulmonary Pharmacoloy: Delivery Devices and Medications, dated Sep. 6, 2017, 2 pages, available at www.cdeu.org/cecourses/z98207/ch4.htm.
Dunn P and Reay D, Heat Pipes, 4th edition, 1994, ISBN 0080419038, 14 pages.
Application and File History for U.S. Appl. No. 13/125,343, filed Apr. 21, 2011 inventor Buchberger.
Japanese Notice of Reasons for Rejection dated Sep. 8, 2015 for Japanese Application No. 2014179732.
Japanese Notice of Reasons for Rejection dated Oct. 15, 2013 for Japanese Application No. 2011532464.
Application and File History for U.S. Appl. No. 14/306,831, filed Jun. 17, 2014, inventor Buchberger.
European Search Report for European Application No. 16166656 dated Oct. 11, 2016.
Notice of Opposition Letter from EPO. Opposition against: EP2358418 dated Mar. 1, 2017.
Rudolph G, BAT Cigarettenfabriken GmbH, 1987, The Influence of CO2 on the Sensory Characteristics of the Favor-System, http://legacy.library.ucsf.edu/tid/sla51f00.
Application and File History for U.S. Appl. No. 15/470,078, filed Mar. 27, 2017, inventor Buchberger.
Application and File History for U.S. Appl. No. 15/470,095, filed Mar. 27, 2017, inventor Buchberger.
International Search Report for International Application No. PCT/AT2009/000413 dated Jan. 25, 2010.
Chinese First Office Action for Chinese Application No. 200980152395.4 dated Dec. 3, 2012.
Chinese Second Office Action for Chinese Application No. 200980152395.4 dated Aug. 20, 2013.
Japanese Reasons for Rejection for Japanese Application No. 2016134648 dated May 23, 2017.
Japanese Decision to Grant, Application No. 2016-134648, dated May 22, 2018, 3 pages (4 pages with translation).
Japanese Office Action, Application No. 2016-564977, dated Dec. 5, 2017, 3 pages (6 pages with translation).
Japanese Search Report, Application No. 2016-864977, dated Oct. 25, 2017, 9 pages (19 pages with translation).
Chinese Office Action, Application No. 201580022356.8, dated Jul. 18, 2018, 8 pages (15 pages with translation).
International Search Report for International Application No. PCT/AT2009/000414 dated Jan. 26, 2010.
Kynol, Kynol Standard Specifications of Activated Carbon Fiber Products, 2 pages, as retrieved on Sep. 19, 2013.
Application and File History for U.S. Appl. No. 14/296,803, filed Jun. 5, 2014 inventor Buchberger.
Application and File History for U.S. Appl. No. 15/454,156, filed Mar. 9, 2017, inventor Buchberger.
International Search Report for corresponding International Application No. PCT/GB2015/051213 dated Jul. 16, 2015; 5 pages.
Written Opinion of the International Searching Authority for corresponding International Application No. PCT/GB2015/051213 dated Jul. 16, 2015; 9 pages.
Written Opinion of the International Preliminary Examining Authority for corresponding International Application No. PCT/GB2015/051213 dated Mar. 29, 2016; 10 pages.
International Preliminary Report on Patentability for corresponding International Application No. PCT/GB2015/051213 dated Jul. 14, 2016; 21 pages.
Chinese Search Report, Application No. 201610086101.4, dated Apr. 25, 2018, 1 page.
Chinese Office Action, 201610086101.4, dated May 4, 2018, 3 pages.
Chinese Office Action and Search Report, Application No. 201610371843.1, dated Sep. 30, 2018, 6 pages (11 pages with translation).
Japanese Decision to Grant, Application No. JP2016-134648, dated May 22, 2018, 6 pages.
International Search Report and Written Opinion, Application No. PCT/GB2017/051139, dated Aug. 9, 2017, 16 pages.
International Preliminary Report on Patentability, Application No. PCT/GB2017/051139, dated Aug. 6, 2018, 8 pages.
Application and File History for U.S. Appl. No. 15/997,113, filed Jun. 4, 2018, Inventor: Buchberger.
Application and File History for U.S. Appl. No. 14/594,065, filed Jan. 9, 2015, Inventor: Buchberger.
Application and File History for U.S. Appl. No. 16/096,554, filed Oct. 25, 2018, Inventor: Fraser.
Company Filtrona Richmond, Inc., www.filtronaporoustechnologies.com, dated Nov. 19, 2008, 1 page.
Japanese Search Report, Application No. 2011-532464, dated Sep. 19, 2013, 116 pages.
Japanese Search Report, Application No. 2014-179732, dated Aug. 25, 2015, 5 pages.
Japanese Search Report, Application No. 2016-134648, dated Apr. 14, 2017, 26 pages.
Russian Decision to Grant, Application No. 2011120430/14, dated Apr. 1, 2014, 10 pages.
European Search Report, Application No. 18205608.5, dated Jul. 12, 2019, 7 pages.
European Communication, Application No. 17189951.1, dated Jan. 25, 2019, 4 pages.
Japanese Office Action and Search Report, Application No. 2018-088088, dated Feb. 28, 2019, 25 pages.
Japanese Decision to Grant, Application No. 2011-532464, dated Aug. 5, 2014, 3 pages (6 pages with translation).
Chinese Notification to Grant Patent, Application No. 201610086101.4, dated Oct. 25, 2018, 2 pages.
Russian Search Report, Application No. 2018137501, dated Apr. 29, 2019, 12 pages.
Russian Search Report, Application No. 2018137583/12, dated Jun. 24, 2019, 2 pages.
Notice of Opposition on behalf of JT International S.A., Opposition against EP 3117860 (Application No. 16166656.5), dated Oct. 30, 2019, 39 pages.
Australian Examination Report, Application No. 2017256084, dated Nov. 20, 2019, 3 pages.
Related Publications (1)
Number Date Country
20170042245 A1 Feb 2017 US