Field of the Invention
[0001] The present invention relates to a vapour generating system for a smoking substitute
apparatus and, in addition, a smoking substitute apparatus that is able to deliver
nicotine to a user in an effective manner.
Background
[0002] The smoking of tobacco is generally considered to expose a smoker to potentially
harmful substances. It is thought that a significant amount of the potentially harmful
substances are generated through the burning and/or combustion of the tobacco and
the constituents of the burnt tobacco in the tobacco smoke itself.
[0003] Low temperature combustion of organic material such as tobacco is known to produce
tar and other potentially harmful by-products. There have been proposed various smoking
substitute systems in which the conventional smoking of tobacco is avoided.
[0004] Such smoking substitute systems can form part of nicotine replacement therapies aimed
at people who wish to stop smoking and overcome a dependence on nicotine.
[0005] Known smoking substitute systems include electronic systems that permit a user to
simulate the act of smoking by producing an aerosol (also referred to as a "vapour")
that is drawn into the lungs through the mouth (inhaled) and then exhaled. The inhaled
aerosol typically bears nicotine and/or a flavourant without, or with fewer of, the
health risks associated with conventional smoking.
[0006] In general, smoking substitute systems are intended to provide a substitute for the
rituals of smoking, whilst providing the user with a similar, or improved, experience
and satisfaction to those experienced with conventional smoking and with combustible
tobacco products.
[0007] The use of smoking substitute systems has grown rapidly in the past few years as
an aid to assist habitual smokers wishing to quit tobacco smoking. There are a number
of different categories of smoking substitute systems, each utilising a different
smoking substitute approach. Some smoking substitute systems are designed to resemble
a conventional cigarette and are cylindrical in form with a mouthpiece at one end.
Other smoking substitute devices do not generally resemble a cigarette (for example,
the smoking substitute device may have a generally box-like form, in whole or in part).
[0008] One approach is the so-called "vaping" approach, in which a vaporisable liquid, or
an aerosol former, sometimes typically referred to herein as "e-liquid", is heated
by a heating device (sometimes referred to herein as an electronic cigarette or "e-cigarette"
device) to produce an aerosol vapour which is inhaled by a user. The e-liquid typically
includes a base liquid, nicotine and may include a flavourant. The resulting vapour
therefore also typically contains nicotine and/or a flavourant. The base liquid may
include propylene glycol and/or vegetable glycerine.
[0009] A typical e-cigarette device includes a mouthpiece, a power source (typically a battery),
a tank for containing e-liquid and a heating device. In use, electrical energy is
supplied from the power source to the heating device, which heats the e-liquid to
produce an aerosol (or "vapour") which is inhaled by a user through the mouthpiece.
[0010] E-cigarettes can be configured in a variety of ways. For example, there are "closed
system" vaping smoking substitute systems, which typically have a sealed tank and
heating element. The tank is prefilled with e-liquid and is not intended to be refilled
by an end user. One subset of closed system vaping smoking substitute systems include
a main body which includes the power source, wherein the main body is configured to
be physically and electrically couplable to a consumable including the tank and the
heating element. In this way, when the tank of a consumable has been emptied of e-liquid,
that consumable is removed from the main body and disposed of. The main body can then
be reused by connecting it to a new, replacement, consumable. Another subset of closed
system vaping smoking substitute systems are completely disposable, and intended for
one-use only.
[0011] There are also "open system" vaping smoking substitute systems which typically have
a tank that is configured to be refilled by a user. In this way the entire device
can be used multiple times.
[0012] An example vaping smoking substitute system is the myblu
™ e-cigarette. The myblu
™ e-cigarette is a closed system which includes a main body and a consumable. The main
body and consumable are physically and electrically coupled together by pushing the
consumable into the main body. The main body includes a rechargeable battery. The
consumable includes a mouthpiece and a sealed tank which contains e-liquid. The consumable
further includes a heater, which for this device is a heating filament coiled around
a portion of a wick. The wick is partially immersed in the e-liquid, and conveys e-liquid
from the tank to the heating filament. The system is controlled by a microprocessor
on board the main body. The system includes a sensor for detecting when a user is
inhaling through the mouthpiece, the microprocessor then activating the device in
response. When the system is activated, electrical energy is supplied from the power
source to the heating device, which heats e-liquid from the tank to produce a vapour
which is inhaled by a user through the mouthpiece.
Summary of the Invention
[0013] It is apparent that the tank or reservoir which contains the e-liquid can only hold
a certain amount of that liquid; once the liquid is used up the tank must be refilled
or discarded. Accordingly maximum efficiency in utilizing all the e-liquid contained
in the tank is a priority for sustainability and user satisfaction.
[0014] Furthermore, during usage, the liquid in the tank is carried by the wick or other
vaporiser element; it is inevitable that in certain conditions some of that liquid
will be lost for example by leakage, displacement through sudden force application
and so on. Such lost liquid can in some circumstances leak from the smoking substitute
apparatus or system, leading either to damage (via corrosion or other effects) or
simply user discomfort.
[0015] It is therefore desirable to limit such leakage and liquid loss.
[0016] The present disclosure has been devised in the light of the above considerations.
[0017] According to a first preferred aspect there is provided a vapour generating system
for use in a smoking substitute apparatus, the system comprising: a reservoir configured
to retain a vaporisable liquid; a wick in contact with the reservoir, the wick configured
to absorb vaporisable liquid from the reservoir; a heater, connected to the wick and
configured to vaporise the vaporisable liquid absorbed by the wick; and an expandable
absorbent body which, in its unexpanded form, is separated from the wick via an air
gap and wherein the expandable absorbent body, in its expanded form, is configured
to contact the wick.
[0018] In some embodiments, the expanded form of the absorbent body corresponds to a form
in which it has expanded by at least 60% of its maximum expansion. In other embodiments,
the expanded form of the absorbent body corresponds to a form in which it has expanded
by at most 40% of its maximum expansion.
[0019] It may be preferred that the system further comprises a cavity, which is sealed from
the reservoir by at least the wick, containing the absorbent body.
[0020] The absorbent body may optionally be provided as an annular cylinder.
[0021] A second preferred aspect of the present invention provides a smoking substitute
apparatus having: an air inlet; an outlet; a flow passage formed between the air inlet
and the outlet; a vapour generating system according to the first aspect; and a vaporisation
chamber in communication with the flow passage, wherein at least part of the wick
and the heater of the vapour generating system are positioned within the vaporization
chamber.
[0022] A third preferred aspect of the present invention provides use of a vapour generating
system as described herein in the generation of a vapour, wherein: in an initial operation
of the system, the reservoir retains the vaporisable liquid and the wick absorbs vaporisable
liquid from the reservoir, and the heater vaporises the vaporisable liquid absorbed
by the wick, the expandable absorbent body being separated from the wick via said
air gap; and during use, the expandable absorbent body gradually captures liquid lost
from the reservoir and/or wick and expands so that, in a subsequent operation of the
system, the expandable absorbent body contacts the wick to allow liquid in the expandable
absorbent body to move into the wick for vaporisation.
[0023] The smoking substitute apparatus may be comprised by or within a cartridge configured
for engagement with a main body, the cartridge and main body together forming a smoking
substitute system. The smoking substitute apparatus may be removably engageable with
the main body (which may also be referred to herein as the base unit).
[0024] The smoking substitute apparatus may be in the form of a consumable. The consumable
may be configured for engagement with a main body. When the consumable is engaged
with the main body, the combination of the consumable and the main body may form a
smoking substitute system such as a closed smoking substitute system. For example,
the consumable may comprise components of the system that are disposable, and the
main body may comprise non-disposable or non-consumable components (e.g. power supply,
controller, sensor, etc.) that facilitate the generation and/or delivery of aerosol
by the consumable. In such an embodiment, the aerosol precursor (e.g. e-liquid) may
be replenished by replacing a used consumable with an unused consumable.
[0025] Alternatively, the smoking substitute apparatus may be a non-consumable apparatus
(e.g. that is in the form of an open smoking substitute system). In such embodiments
an aerosol former (e.g. e-liquid) of the system may be replenished by re-filling,
e.g. a reservoir of the smoking substitute apparatus, with the aerosol precursor (rather
than replacing a consumable component of the apparatus).
[0026] In light of this, it should be appreciated that some of the features described herein
as being part of the smoking substitute apparatus may alternatively form part of a
main body for engagement with the smoking substitute apparatus. This may be the case
in particular when the smoking substitute apparatus is in the form of a consumable.
[0027] Where the smoking substitute apparatus is in the form of a consumable, the main body
and the consumable may be configured to be physically coupled together. For example,
the consumable may be at least partially received in a recess of the main body, such
that there is an interference fit between the main body and the consumable. Alternatively,
the main body and the consumable may be physically coupled together by screwing one
onto the other, or through a bayonet fitting, or the like.
[0028] Thus, the smoking substitute apparatus may comprise one or more engagement portions
for engaging with a main body. In this way, one end of the smoking substitute apparatus
may be coupled with the main body, whilst an opposing end of the smoking substitute
apparatus may define a mouthpiece of the smoking substitute system.
[0029] In the present invention, the vapour generating system comprises a reservoir configured
to store an aerosol precursor, such as an e-liquid. The e-liquid may, for example,
comprise a base liquid. The e-liquid may further comprise nicotine. The base liquid
may include propylene glycol and/or vegetable glycerine. The e-liquid may be substantially
flavourless. That is, the e-liquid may not contain any deliberately added additional
flavourant and may consist solely of a base liquid of propylene glycol and/or vegetable
glycerine and nicotine.
[0030] The reservoir may be in the form of a tank. At least a portion of the tank may be
light-transmissive. For example, the tank may comprise a window to allow a user to
visually assess the quantity of e-liquid in the tank. A housing of the smoking substitute
apparatus may comprise a corresponding aperture (or slot) or window that may be aligned
with a light-transmissive portion (e.g. window) of the tank. The reservoir may be
referred to as a "clearomizer" if it includes a window, or a "cartomizer" if it does
not.
[0031] The outlet may be at a mouthpiece of the smoking substitute apparatus. In this respect,
a user may draw fluid (e.g. air) into and through the passage by inhaling at the outlet
(i.e. using the mouthpiece). The passage may be at least partially defined by the
tank. The tank may substantially (or fully) define the passage, for at least a part
of the length of the passage. In this respect, the tank may surround the passage,
e.g. in an annular arrangement around the passage.
[0032] Alternatively or additionally, a cavity containing the present absorbent body may
substantially (or fully) define the passage, for at least a part of the length of
the passage. In this respect, the cavity may surround the passage, e.g. in an annular
arrangement around the passage.
[0033] The vaporisation chamber may be arranged to be in fluid communication with the inlet
and outlet of the passage. The vaporisation chamber may be an enlarged portion of
the passage. In this respect, the air as drawn in by the user may entrain the generated
vapour in a flow away from heater. The entrained vapour may form an aerosol in the
vaporisation chamber, or it may form the aerosol further downstream along the passage.
The vaporisation chamber may be at least partially defined by the tank. The tank may
substantially (or fully) define the vaporisation chamber, and thus may form the enclosure.
In this respect, the tank may surround the vaporisation chamber, e.g. in an annular
arrangement around the vaporisation chamber.
[0034] In use, the user may puff on a mouthpiece of the smoking substitute apparatus, i.e.
draw on the smoking substitute apparatus by inhaling, to draw in an air stream therethrough.
The part of the air flow which bypasses the vaporisation chamber (dilution air flow)
may combine with the other part of the air flow (main air flow) for diluting the aerosol
contained therein. The dilution air flow may be directly inhaled by the user without
passing through the passage of the smoking substitute apparatus.
[0035] As a user puffs on the mouthpiece, vaporised e-liquid entrained in the passing air
flow may be drawn towards the outlet of the passage. The vapour may cool, and thereby
nucleate and/or condense along the passage to form a plurality of aerosol droplets,
e.g. nicotine-containing aerosol droplets. A portion of these aerosol droplets may
be delivered to and be absorbed at a target delivery site, e.g. a user's lung, whilst
a portion of the aerosol droplets may instead adhere onto other parts of the user's
respiratory tract, e.g. the user's oral cavity and/or throat. Typically, in some known
smoking substitute apparatuses, the aerosol droplets as measured at the outlet of
the passage, e.g. at the mouthpiece, may have a droplet size, dso, of less than 1µm.
[0036] In some embodiments of the invention, the dso particle size of the aerosol particles
is preferably at least 1 µm, more preferably at least 2 µm. Typically, the dso particle
size is not more than 10 µm, preferably not more than 9 µm, not more than 8 µm, not
more than 7 µm, not more than 6 µm, not more than 5 µm, not more than 4 µm or not
more than 3 µm. It is considered that providing aerosol particle sizes in such ranges
permits improved interaction between the aerosol particles and the user's lungs.
[0037] The particle droplet size, dso, of an aerosol may be measured by a laser diffraction
technique. For example, the stream of aerosol output from the outlet of the passage
may be drawn through a Malvern Spraytec laser diffraction system, where the intensity
and pattern of scattered laser light are analysed to calculate the size and size distribution
of aerosol droplets. As will be readily understood, the particle size distribution
may be expressed in terms of d
10, dso and d
90, for example. Considering a cumulative plot of the volume of the particles measured
by the laser diffraction technique, the d
10 particle size is the particle size below which 10% by volume of the sample lies.
The dso particle size is the particle size below which 50% by volume of the sample
lies. The d
90 particle size is the particle size below which 90% by volume of the sample lies.
Unless otherwise indicated herein, the particle size measurements are volume-based
particle size measurements, rather than number-based or mass-based particle size measurements.
[0038] The spread of particle size may be expressed in terms of the span, which is defined
as (d
90-d
10)/d
50. Typically, the span is not more than 20, preferably not more than 10, preferably
not more than 8, preferably not more than 4, preferably not more than 2, preferably
not more than 1, or not more than 0.5.
[0039] The smoking substitute apparatus (or main body engaged with the smoking substitute
apparatus) may comprise a power source. The power source may be electrically connected
(or connectable) to a heater of the smoking substitute apparatus (e.g. when the smoking
substitute apparatus is engaged with the main body). The power source may be a battery
(e.g. a rechargeable battery). A connector in the form of e.g. a USB port may be provided
for recharging this battery.
[0040] When the smoking substitute apparatus is in the form of a consumable, the smoking
substitute apparatus may comprise an electrical interface for interfacing with a corresponding
electrical interface of the main body. One or both of the electrical interfaces may
include one or more electrical contacts. Thus, when the main body is engaged with
the consumable, the electrical interface of the main body may be configured to transfer
electrical power from the power source to a heater of the consumable via the electrical
interface of the consumable.
[0041] The electrical interface of the smoking substitute apparatus may also be used to
identify the smoking substitute apparatus (in the form of a consumable) from a list
of known types. For example, the consumable may have a certain concentration of nicotine
and the electrical interface may be used to identify this. The electrical interface
may additionally or alternatively be used to identify when a consumable is connected
to the main body.
[0042] Again, where the smoking substitute apparatus is in the form of a consumable, the
main body may comprise an identification means, which may, for example, be in the
form of an RFID reader, a barcode or QR code reader. This identification means may
be able to identify a characteristic (e.g. a type) of a consumable engaged with the
main body. In this respect, the consumable may include any one or more of an RFID
chip, a barcode or QR code, or memory within which is an identifier and which can
be interrogated via the identification means.
[0043] The smoking substitute apparatus or main body may comprise a controller, which may
include a microprocessor. The controller may be configured to control the supply of
power from the power source to the heater of the smoking substitute apparatus (e.g.
via the electrical contacts). A memory may be provided and may be operatively connected
to the controller. The memory may include non-volatile memory. The memory may include
instructions which, when implemented, cause the controller to perform certain tasks
or steps of a method.
[0044] The main body or smoking substitute apparatus may comprise a wireless interface,
which may be configured to communicate wirelessly with another device, for example
a mobile device, e.g. via Bluetooth
®. To this end, the wireless interface could include a Bluetooth
® antenna. Other wireless communication interfaces, e.g. WiFi
®, are also possible. The wireless interface may also be configured to communicate
wirelessly with a remote server.
[0045] A puff sensor may be provided that is configured to detect a puff (i.e. inhalation
from a user). The puff sensor may be operatively connected to the controller so as
to be able to provide a signal to the controller that is indicative of a puff state
(i.e. puffing or not puffing). The puff sensor may, for example, be in the form of
a pressure sensor or an acoustic sensor. That is, the controller may control power
supply to the heater of the consumable in response to a puff detection by the sensor.
The control may be in the form of activation of the heater in response to a detected
puff. That is, the smoking substitute apparatus may be configured to be activated
when a puff is detected by the puff sensor. When the smoking substitute apparatus
is in the form of a consumable, the puff sensor may be provided in the consumable
or alternatively may be provided in the main body.
[0046] The term "flavourant" is used to describe a compound or combination of compounds
that provide flavour and/or aroma. For example, the flavourant may be configured to
interact with a sensory receptor of a user (such as an olfactory or taste receptor).
The flavourant may include one or more volatile substances.
[0047] The flavourant may be provided in solid or liquid form. The flavourant may be natural
or synthetic. For example, the flavourant may include menthol, liquorice, chocolate,
fruit flavour (including e.g. citrus, cherry etc.), vanilla, spice (e.g. ginger, cinnamon)
and tobacco flavour. The flavourant may be evenly dispersed or may be provided in
isolated locations and/or varying concentrations.
[0048] The present inventors consider that a flow rate of 1.3 L min
-1 is towards the lower end of a typical user expectation of flow rate through a conventional
cigarette and therefore through a user-acceptable smoking substitute apparatus. The
present inventors further consider that a flow rate of 2.0 L min
-1 is towards the higher end of a typical user expectation of flow rate through a conventional
cigarette and therefore through a user-acceptable smoking substitute apparatus. Embodiments
of the present invention therefore provide an aerosol with advantageous particle size
characteristics across a range of flow rates of air through the apparatus.
[0049] The aerosol may have a Dv50 of at least 1.1 µm, at least 1.2 µm, at least 1.3 µm,
at least 1.4 µm, at least 1.5 µm, at least 1.6 µm, at least 1.7 µm, at least 1.8 µm,
at least 1.9 µm or at least 2.0 µm.
[0050] The aerosol may have a Dv50 of not more than 4.9 µm, not more than 4.8 µm, not more
than 4.7 µm, not more than 4.6 µm, not more than 4.5 µm, not more than 4.4 µm, not
more than 4.3 µm, not more than 4.2 µm, not more than 4.1 µm, not more than 4.0 µm,
not more than 3.9 µm, not more than 3.8 µm, not more than 3.7 µm, not more than 3.6
µm, not more than 3.5 µm, not more than 3.4 µm, not more than 3.3 µm, not more than
3.2 µm, not more than 3.1 µm or not more than 3.0 µm.
[0051] A particularly preferred range for Dv50 of the aerosol is in the range 2-3 µm.
[0052] The air inlet, flow passage, outlet, and the vaporisation chamber may be configured
so that, when the air flow rate inhaled by the user through the apparatus is 1.3 L
min
-1, the average magnitude of velocity of air in the vaporisation chamber is in the range
0-1.3 ms
-1. The average magnitude velocity of air may be calculated based on knowledge of the
geometry of the vaporisation chamber, and the flow rate.
[0053] When the air flow rate inhaled by the user through the apparatus is 1.3 L min
-1, the average magnitude of velocity of air in the vaporisation chamber may be at least
0.001 ms
-1, or at least 0.005 ms
-1, or at least 0.01 ms
-1, or at least 0.05 ms
-1.
[0054] When the air flow rate inhaled by the user through the apparatus is 1.3 L min
-1, the average magnitude of velocity of air in the vaporisation chamber may be at most
1.2 ms
-1, at most 1.1 ms
-1, at most 1.0 ms
-1, at most 0.9 ms
-1, at most 0.8 ms
-1, at most 0.7 ms
-1 or at most 0.6 ms
-1.
[0055] The air inlet, flow passage, outlet, and the vaporisation chamber may be configured
so that, when the air flow rate inhaled by the user through the apparatus is 2.0 L
min
-1, the average magnitude of velocity of air in the vaporisation chamber is in the range
0-1.3 ms
-1. The average magnitude velocity of air may be calculated based on knowledge of the
geometry of the vaporisation chamber, and the flow rate.
[0056] When the air flow rate inhaled by the user through the apparatus is 2.0 L min
-1, the average magnitude of velocity of air in the vaporisation chamber may be at least
0.001 ms
-1, or at least 0.005 ms
-1, or at least 0.01 ms
-1, or at least 0.05 ms
-1.
[0057] When the airflow rate inhaled by the user through the apparatus is 2.0 L min
-1, the average magnitude of velocity of air in the vaporisation chamber may be at most
1.2 ms
-1, at most 1.1 ms
-1, at most 1.0 ms
-1, at most 0.9 ms
-1, at most 0.8 ms
-1, at most 0.7 ms
-1 or at most 0.6 ms
-1.
[0058] When the calculated average magnitude of velocity of air in the vaporisation chamber
is in the ranges specified, it is considered that the resultant aerosol particle size
is advantageously controlled to be in a desirable range. It is further considered
that the configuration of the apparatus can be selected so that the average magnitude
of velocity of air in the vaporisation chamber can be brought within the ranges specified,
at the exemplary flow rate of 1.3 L min
-1 and/or the exemplary flow rate of 2.0 L min
-1.
[0059] The aerosol generator described herein comprises a vaporiser element which can be
loaded with aerosol precursor, the vaporiser element being heatable by a heater and
presenting a vaporiser element surface to air in the vaporisation chamber. A vaporiser
element region may be defined as a volume extending outwardly from the vaporiser element
surface to a distance of 1 mm from the vaporiser element surface.
[0060] The air inlet, flow passage, outlet, and the vaporisation chamber may be configured
so that, when the air flow rate inhaled by the user through the apparatus is 1.3 L
min
-1, the average magnitude of velocity of air in the vaporiser element region is in the
range 0-1.2 ms
-1. The average magnitude of velocity of air in the vaporiser element region may be
calculated using computational fluid dynamics.
[0061] When the air flow rate inhaled by the user through the apparatus is 1.3 L min
-1, the average magnitude of velocity of air in the vaporiser element region may be
at least 0.001 ms
-1, or at least 0.005 ms
-1, or at least 0.01 ms
-1, or at least 0.05 ms
-1.
[0062] When the air flow rate inhaled by the user through the apparatus is 1.3 L min
-1, the average magnitude of velocity of air in the vaporiser element region may be
at most 1.1 ms
-1, at most 1.0 ms
-1, at most 0.9 ms
-1, at most 0.8 ms
-1, at most 0.7 ms
-1 or at most 0.6 ms
-1.
[0063] The air inlet, flow passage, outlet, and the vaporisation chamber may be configured
so that, when the air flow rate inhaled by the user through the apparatus is 2.0 L
min
-1, the average magnitude of velocity of air in the vaporiser element region is in the
range 0-1.2 ms
-1. The average magnitude of velocity of air in the vaporiser element region may be
calculated using computational fluid dynamics.
[0064] When the airflow rate inhaled by the user through the apparatus is 2.0 L min
-1, the average magnitude of velocity of air in the vaporiser element region may be
at least 0.001 ms
-1, or at least 0.005 ms
-1, or at least 0.01 ms
-1, or at least 0.05 ms
-1.
[0065] When the airflow rate inhaled by the user through the apparatus is 2.0 L min
-1, the average magnitude of velocity of air in the vaporiser element region may be
at most 1.1 ms
-1, at most 1.0 ms
-1, at most 0.9 ms
-1, at most 0.8 ms
-1, at most 0.7 ms
-1 or at most 0.6 ms
-1.
[0066] When the average magnitude of velocity of air in the vaporiser element region is
in the ranges specified, it is considered that the resultant aerosol particle size
is advantageously controlled to be in a desirable range. It is further considered
that the velocity of air in the vaporiser element region is more relevant to the resultant
particle size characteristics than consideration of the velocity in the vaporisation
chamber as a whole. This is in view of the significant effect of the velocity of air
in the vaporiser element region on the cooling of the vapour emitted from the vaporiser
element surface.
[0067] Additionally or alternatively is it relevant to consider the maximum magnitude of
velocity of air in the vaporiser element region.
[0068] Therefore, the air inlet, flow passage, outlet, and the vaporisation chamber may
be configured so that, when the air flow rate inhaled by the user through the apparatus
is 1.3 L min
-1, the maximum magnitude of velocity of air in the vaporiser element region is in the
range 0-2.0 ms
-1.
[0069] When the air flow rate inhaled by the user through the apparatus is 1.3 L min
-1, the maximum magnitude of velocity of air in the vaporiser element region may be
at least 0.001 ms
-1, or at least 0.005 ms
-1, or at least 0.01 ms
-1, or at least 0.05 ms
-1.
[0070] When the air flow rate inhaled by the user through the apparatus is 1.3 L min
-1, the maximum magnitude of velocity of air in the vaporiser element region may be
at most 1.9 ms
-1, at most 1.8 ms
-1, at most 1.7 ms
-1, at most 1.6 ms
-1, at most 1.5 ms
-1, at most 1.4 ms
-1, at most 1.3 ms
-1 or at most 1.2 ms
-1.
[0071] The air inlet, flow passage, outlet, and the vaporisation chamber may be configured
so that, when the air flow rate inhaled by the user through the apparatus is 2.0 L
min
-1, the maximum magnitude of velocity of air in the vaporiser element region is in the
range 0-2.0 ms
-1.
[0072] When the air flow rate inhaled by the user through the apparatus is 2.0 L min
-1, the maximum magnitude of velocity of air in the vaporiser element region may be
at least 0.001 ms
-1, or at least 0.005 ms
-1, or at least 0.01 ms
-1, or at least 0.05 ms
-1.
[0073] When the air flow rate inhaled by the user through the apparatus is 2.0 L min
-1, the maximum magnitude of velocity of air in the vaporiser element region may be
at most 1.9 ms
-1, at most 1.8 ms
-1, at most 1.7 ms
-1, at most 1.6 ms
-1, at most 1.5 ms
-1, at most 1.4 ms
-1, at most 1.3 ms
-1 or at most 1.2 ms
-1.
[0074] It is considered that configuring the apparatus in a manner to permit such control
of velocity of the airflow at the vaporiser permits the generation of aerosols with
particularly advantageous particle size characteristics, including Dv50 values.
[0075] Additionally or alternatively is it relevant to consider the turbulence intensity
in the vaporiser chamber in view of the effect of turbulence on the particle size
of the generated aerosol. For example, the air inlet, flow passage, outlet, and the
vaporisation chamber may be configured so that, when the air flow rate inhaled by
the user through the apparatus is 1.3 L min
-1, the turbulence intensity in the vaporiser element region is not more than 1%.
[0076] When the air flow rate inhaled by the user through the apparatus is 1.3 L min
-1, the turbulence intensity in the vaporiser element region may be not more than 0.95%,
not more than 0.9%, not more than 0.85%, not more than 0.8%, not more than 0.75%,
not more than 0.7%, not more than 0.65% or not more than 0.6%.
[0077] It is considered that configuring the apparatus in a manner to permit such control
of the turbulence intensity in the vaporiser element region permits the generation
of aerosols with particularly advantageous particle size characteristics, including
Dv50 values.
[0078] Following detailed investigations, the inventors consider, without wishing to be
bound by theory, that the particle size characteristics of the generated aerosol may
be determined by the cooling rate experienced by the vapour after emission from the
vaporiser element (e.g. wick). In particular, it appears that imposing a relatively
slow cooling rate on the vapour has the effect of generating aerosols with a relatively
large particle size. The parameters discussed above (velocity and turbulence intensity)
are considered to be mechanisms for implementing a particular cooling dynamic to the
vapour.
[0079] More generally, it is considered that the air inlet, flow passage, outlet, and the
vaporisation chamber may be configured so that a desired cooling rate is imposed on
the vapour. The particular cooling rate to be used depends of course on the nature
of the aerosol precursor and other conditions. However, for a particular aerosol precursor
it is possible to define a set of testing conditions in order to define the cooling
rate, and by extension this imposes limitations on the configuration of the apparatus
to permit such cooling rates as are shown to result in advantageous aerosols. Accordingly,
the air inlet, flow passage, outlet, and the vaporisation chamber may be configured
so that the cooling rate of the vapour is such that the time taken to cool to 50 °C
is not less than 16 ms, when tested according to the following protocol. The aerosol
precursor is an e-liquid consisting of 1.6% freebase nicotine and the remainder a
65:35 propylene glycol and vegetable glycerine mixture, the e-liquid having a boiling
point of 209 °C. Air is drawn into the air inlet at a temperature of 25 °C. The vaporiser
is operated to release a vapour of total particulate mass 5 mg over a 3 second duration
from the vaporiser element surface in an air flow rate between the air inlet and outlet
of 1.3 L min
-1.
[0080] Additionally or alternatively, the air inlet, flow passage, outlet, and the vaporisation
chamber may be configured so that the cooling rate of the vapour is such that the
time taken to cool to 50 °C is not less than 16 ms, when tested according to the following
protocol. The aerosol precursor is an e-liquid consisting of 1.6% freebase nicotine
and the remainder a 65:35 propylene glycol and vegetable glycerine mixture, the e-liquid
having a boiling point of 209 °C. Air is drawn into the air inlet at a temperature
of 25 °C. The vaporiser is operated to release a vapour of total particulate mass
5 mg over a 3 second duration from the vaporiser element surface in an air flow rate
between the air inlet and outlet of 2.0 L min
-1.
[0081] Cooling of the vapour such that the time taken to cool to 50 °C is not less than
16 ms corresponds to an equivalent linear cooling rate of not more than 10 °C/ms.
[0082] The equivalent linear cooling rate of the vapour to 50 °C may be not more than 9
°C/ms, not more than 8 °C/ms, not more than 7 °C/ms, not more than 6 °C/ms or not
more than 5 °C/ms.
[0083] Cooling of the vapour such that the time taken to cool to 50 °C is not less than
32 ms corresponds to an equivalent linear cooling rate of not more than 5 °C/ms.
[0084] The testing protocol set out above considers the cooling of the vapour (and subsequent
aerosol) to a temperature of 50 °C. This is a temperature which can be considered
to be suitable for an aerosol to exit the apparatus for inhalation by a user without
causing significant discomfort. It is also possible to consider cooling of the vapour
(and subsequent aerosol) to a temperature of 75 °C. Although this temperature is possibly
too high for comfortable inhalation, it is considered that the particle size characteristics
of the aerosol are substantially settled by the time the aerosol cools to this temperature
(and they may be settled at still higher temperature).
[0085] Accordingly, the air inlet, flow passage, outlet, and the vaporisation chamber may
be configured so that the cooling rate of the vapour is such that the time taken to
cool to 75 °C is not less than 4.5 ms, when tested according to the following protocol.
The aerosol precursor is an e-liquid consisting of 1.6% freebase nicotine and the
remainder a 65:35 propylene glycol and vegetable glycerine mixture, the e-liquid having
a boiling point of 209 °C. Air is drawn into the air inlet at a temperature of 25
°C. The vaporiser is operated to release a vapour of total particulate mass 5 mg over
a 3 second duration from the vaporiser element surface in an air flow rate between
the air inlet and outlet of 1.3 L min
-1.
[0086] Additionally or alternatively, the air inlet, flow passage, outlet, and the vaporisation
chamber may be configured so that the cooling rate of the vapour is such that the
time taken to cool to 75 °C is not less than 4.5 ms, when tested according to the
following protocol. The aerosol precursor is an e-liquid consisting of 1.6% freebase
nicotine and the remainder a 65:35 propylene glycol and vegetable glycerine mixture,
the e-liquid having a boiling point of 209 °C. Air is drawn into the air inlet at
a temperature of 25 °C. The vaporiser is operated to release a vapour of total particulate
mass 5 mg over a 3 second duration from the vaporiser element surface in an air flow
rate between the air inlet and outlet of 2.0 L min
-1.
[0087] Cooling of the vapour such that the time taken to cool to 75 °C is not less than
4.5 ms corresponds to an equivalent linear cooling rate of not more than 30 °C/ms.
[0088] The equivalent linear cooling rate of the vapour to 75 °C may be not more than 29
°C/ms, not more than 28 °C/ms, not more than 27 °C/ms, not more than 26 °C/ms, not
more than 25 °C/ms, not more than 24 °C/ms, not more than 23 °C/ms, not more than
22 °C/ms, not more than 21 °C/ms, not more than 20 °C/ms, not more than 19 °C/ms,
not more than 18 °C/ms, not more than 17 °C/ms, not more than 16 °C/ms, not more than
15 °C/ms, not more than 14 °C/ms, not more than 13 °C/ms, not more than 12 °C/ms,
not more than 11 °C/ms or not more than 10 °C/ms.
[0089] Cooling of the vapour such that the time taken to cool to 75 °C is not less than
13 ms corresponds to an equivalent linear cooling rate of not more than 10 °C/ms.
[0090] It is considered that configuring the apparatus in a manner to permit such control
of the cooling rate of the vapour permits the generation of aerosols with particularly
advantageous particle size characteristics, including Dv50 values.
[0091] The invention includes the combination of the aspects and preferred features described
except where such a combination is clearly impermissible or expressly avoided.
Summary of the Figures
[0092]
Figure 1 is a schematic front view of a smoking substitute system, according to a
first reference arrangement, in an engaged position;
Figure 2 is a schematic front view of the smoking substitute system of the first reference
arrangement in a disengaged position;
Figure 3 is a schematic longitudinal cross sectional view of a smoking substitute
apparatus of the first reference arrangement;
Figure 4 is an enlarged schematic cross sectional view of part of the air passage
and vaporisation chamber of the first reference arrangement;
Figure 5 shows a schematic cross sectional view of a smoking substitute apparatus
of a second reference arrangement;
Figure 6 shows a schematic cross sectional view of a smoking substitute apparatus
of a third reference arrangement;
Figure 7A shows a schematic cross sectional view of a smoking substitute apparatus
of the present invention, with the absorbent material in the unexpanded position;
and Figure 7B shows a schematic cross sectional view of the same smoking substitute
apparatus with the absorbent material in the expanded position.
Detailed Description of the Invention
[0093] Further background to the present invention and further aspects and embodiments of
the present invention will now be discussed with reference to the accompanying figures.
Further aspects and embodiments will be apparent to those skilled in the art. The
contents of all documents mentioned in this text are incorporated herein by reference
in their entirety.
[0094] Figures 1 and 2 illustrate a smoking substitute system in the form of an e-cigarette
system 110. The system 110 comprises a main body 120 of the system 110, and a smoking
substitute apparatus in the form of an e-cigarette consumable (or "pod") 150. In the
illustrated reference arrangement the consumable 150 (sometimes referred to herein
as a smoking substitute apparatus) is removable from the main body 120, so as to be
a replaceable component of the system 110. The e-cigarette system 110 is a closed
system in the sense that it is not intended that the consumable should be refillable
with e-liquid by a user.
[0095] As is apparent from Figures 1 and 2, the consumable 150 is configured to engage the
main body 120. Figure 1 shows the main body 120 and the consumable 150 in an engaged
state, whilst Figure 2 shows the main body 120 and the consumable 150 in a disengaged
state. When engaged, a portion of the consumable 150 is received in a cavity of corresponding
shape in the main body 120 and is retained in the engaged position by way of a snap-engagement
mechanism. In other embodiments, the main body 120 and consumable 150 may be engaged
by screwing one into (or onto) the other, or through a bayonet fitting, or by way
of an interference fit.
[0096] The system 110 is configured to vaporise an aerosol precursor, which in the illustrated
reference arrangement is in the form of a nicotine-based e-liquid 160. The e-liquid
160 comprises nicotine and a base liquid including propylene glycol and/or vegetable
glycerine. In the present embodiment, the e-liquid 160 is flavoured by a flavourant.
In other embodiments, the e-liquid 160 may be flavourless and thus may not include
any added flavourant.
[0097] Figure 3 shows a schematic longitudinal cross sectional view of a reference arrangement
of the smoking substitute apparatus forming part of the smoking substitute system
shown in Figures 1 and 2. In Figure 3, the e-liquid 160 is stored within a reservoir
in the form of a tank 152 that forms part of the consumable 150. In the illustrated
reference arrangement, the consumable 150 is a "single-use" consumable 150. That is,
upon exhausting the e-liquid 160 in the tank 152, the intention is that the user disposes
of the entire consumable 150. The term "single-use" does not necessarily mean the
consumable is designed to be disposed of after a single smoking session. Rather, it
defines the consumable 150 is not arranged to be refilled after the e-liquid contained
in the tank 152 is depleted. The tank may include a vent (not shown) to allow ingress
of air to replace e-liquid that has been used from the tank. The consumable 150 preferably
includes a window 158 (see Figures 1 and 2), so that the amount of e-liquid in the
tank 152 can be visually assessed. The main body 120 includes a slot 157 so that the
window 158 of the consumable 150 can be seen whilst the rest of the tank 152 is obscured
from view when the consumable 150 is received in the cavity of the main body 120.
The consumable 150 may be referred to as a "clearomizer" when it includes a window
158, or a "cartomizer" when it does not.
[0098] In some embodiments, the e-liquid (i.e. aerosol precursor) may be the only part of
the system that is truly "single-use". That is, the tank may be refillable with e-liquid
or the e-liquid may be stored in a non-consumable component of the system. For example,
in such embodiments, the e-liquid may be stored in a tank located in the main body
or stored in another component that is itself not single-use (e.g. a refillable cartomizer).
[0099] The external wall of tank 152 is provided by a casing of the consumable 150. The
tank 152 annularly surrounds, and thus defines a portion of, a passage 170 that extends
between a vaporiser inlet 172 and an outlet 174 at opposing ends of the consumable
150. In this respect, the passage 170 comprises an upstream end at the end of the
consumable 150 that engages with the main body 120, and a downstream end at an opposing
end of the consumable 150 that comprises a mouthpiece 154 of the system 110.
[0100] When the consumable 150 is received in the cavity of the main body 120 as shown in
Figure 3, a plurality of device air inlets 176 are formed at the boundary between
the casing of the consumable and the casing of the main body. The device air inlets
176 are in fluid communication with the vaporiser inlet 172 through an inlet flow
channel 178 formed in the cavity of the main body which is of corresponding shape
to receive a part of the consumable 150. Air from outside of the system 110 can therefore
be drawn into the passage 170 through the device air inlets 176 and the inlet flow
channels 178.
[0101] When the consumable 150 is engaged with the main body 120, a user can inhale (i.e.
take a puff) via the mouthpiece 154 so as to draw air through the passage 170, and
so as to form an airflow (indicated by the dashed arrows in Figure 3) in a direction
from the vaporiser inlet 172 to the outlet 174. Although not illustrated, the passage
170 may be partially defined by a tube (e.g. a metal tube) extending through the consumable
150. In Figure 3, for simplicity, the passage 170 is shown with a substantially circular
cross-sectional profile with a constant diameter along its length. In some embodiments,
the passage may have other cross-sectional profiles, such as oval shaped or polygonal
shaped profiles. Further, in other embodiments, the cross sectional profile and the
diameter (or hydraulic diameter) of the passage may vary along its longitudinal axis.
[0102] The smoking substitute system 110 is configured to vaporise the e-liquid 160 for
inhalation by a user. To provide this operability, the consumable 150 comprises a
heater having a porous wick 162 and a resistive heating element in the form of a heating
filament 164 that is helically wound (in the form of a coil) around a portion of the
porous wick 162. The porous wick 162 extends across the passage 170 (i.e. transverse
to a longitudinal axis of the passage 170 and thus also transverse to the air flow
along the passage 170 during use) and opposing ends of the wick 162 extend into the
tank 152 (so as to be immersed in the e-liquid 160). In this way, e-liquid 160 contained
in the tank 152 is conveyed from the opposing ends of the porous wick 162 to a central
portion of the porous wick 162 so as to be exposed to the airflow in the passage 170.
[0103] The helical filament 164 is wound about the exposed central portion of the porous
wick 162 and is electrically connected to an electrical interface in the form of electrical
contacts 156 mounted at the end of the consumable that is proximate the main body
120 (when the consumable and the main body are engaged). When the consumable 150 is
engaged with the main body 120, electrical contacts 156 make contact with corresponding
electrical contacts (not shown) of the main body 120. The main body electrical contacts
are electrically connectable to a power source (not shown) of the main body 120, such
that (in the engaged position) the filament 164 is electrically connectable to the
power source. In this way, power can be supplied by the main body 120 to the filament
164 in order to heat the filament 164. This heats the porous wick 162 which causes
e-liquid 160 conveyed by the porous wick 162 to vaporise and thus to be released from
the porous wick 162. The vaporised e-liquid becomes entrained in the airflow and,
as it cools in the airflow (between the heated wick and the outlet 174 of the passage
170), condenses to form an aerosol. This aerosol is then inhaled, via the mouthpiece
154, by a user of the system 110. As e-liquid is lost from the heated portion of the
wick, further e-liquid is drawn along the wick from the tank to replace the e-liquid
lost from the heated portion of the wick.
[0104] The filament 164 and the exposed central portion of the porous wick 162 are positioned
across the passage 170. More specifically, the part of passage that contains the filament
164 and the exposed portion of the porous wick 162 forms a vaporisation chamber. In
the illustrated example, the vaporisation chamber has the same cross-sectional diameter
as the passage 170. However, in some embodiments the vaporisation chamber may have
a different cross sectional profile compared with the passage 170. For example, the
vaporisation chamber may have a larger cross sectional diameter than at least some
of the downstream part of the passage 170 so as to enable a longer residence time
for the air inside the vaporisation chamber.
[0105] Figure 4 illustrates in more detail the vaporisation chamber and therefore the region
of the consumable 150 around the wick 162 and filament 164. The helical filament 164
is wound around a central portion of the porous wick 162. The porous wick extends
across passage 170. E-liquid 160 contained within the tank 152 is conveyed as illustrated
schematically by arrows 401, i.e. from the tank and towards the central portion of
the porous wick 162.
[0106] When the user inhales, air is drawn from through the inlets 176 shown in Figure 3,
along inlet flow channel 178 to vaporisation chamber inlet 172 and into the vaporisation
chamber containing porous wick 162. The porous wick 162 extends substantially transverse
to the airflow direction. The airflow passes around the porous wick, at least a portion
of the airflow substantially following the surface of the porous wick 162. In examples
where the porous wick has a cylindrical cross-sectional profile, the airflow may follow
a curved path around an outer periphery of the porous wick 162.
[0107] At substantially the same time as the airflow passes around the porous wick 162,
the filament 164 is heated so as to vaporise the e-liquid which has been wicked into
the porous wick. The airflow passing around the porous wick 162 picks up this vaporised
e-liquid, and the vapour-containing airflow is drawn in direction 403 further down
passage 170.
[0108] The power source of the main body 120 may be in the form of a battery (e.g. a rechargeable
battery such as a lithium ion battery). The main body 120 may comprise a connector
in the form of e.g. a USB port for recharging this battery. The main body 120 may
also comprise a controller that controls the supply of power from the power source
to the main body electrical contacts (and thus to the filament 164). That is, the
controller may be configured to control a voltage applied across the main body electrical
contacts, and thus the voltage applied across the filament 164. In this way, the filament
164 may only be heated under certain conditions (e.g. during a puff and/or only when
the system is in an active state). In this respect, the main body 120 may include
a puff sensor (not shown) that is configured to detect a puff (i.e. inhalation). The
puff sensor may be operatively connected to the controller so as to be able to provide
a signal, to the controller, which is indicative of a puff state (i.e. puffing or
not puffing). The puff sensor may, for example, be in the form of a pressure sensor
or an acoustic sensor.
[0109] Although not shown, the main body 120 and consumable 150 may comprise a further interface
which may, for example, be in the form of an RFID reader, a barcode or QR code reader.
This interface may be able to identify a characteristic (e.g. a type) of a consumable
150 engaged with the main body 120. In this respect, the consumable 150 may include
any one or more of an RFID chip, a barcode or QR code, or memory within which is an
identifier and which can be interrogated via the interface.
[0110] An apparatus according to an embodiment of the invention may be configured such that
in use, at least part of the air flow drawn by a user through the apparatus from the
air inlet to the outlet bypasses the vaporisation chamber defined by the enclosure.
A second reference arrangement of an apparatus, shown in Figure 5, provides an example
of how such a bypassing air flow may be created. Accordingly, some embodiments of
the invention may include one or a combination of the features of the second reference
arrangement (and variations thereof) where such features are combinable with the present
invention. This second reference arrangement is described below.
[0111] Figure 5 illustrates a schematic longitudinal cross sectional view of a second reference
arrangement of the smoking substitute apparatus forming part of the smoking substitute
system shown in Figures 1 and 2. The arrangement illustrated in Figure 5 differs from
the first reference arrangement illustrated in Figure 3 in that the substitute smoking
apparatus includes two bypass passages 180 in addition to the vaporiser passage 170.
The bypass air passages extend between the plurality of device air inlets 176 and
two outlets 184. In other variations of the second reference arrangement, the number
of bypass passages 180 and corresponding outlets 184 may be greater or smaller than
in the illustrated example. Furthermore, there may be more or fewer air inlets and
there may be more or fewer outlets.
[0112] In Figure 5 for simplicity, the bypass passage 180 is shown with a substantially
circular cross-sectional profile with a constant diameter along its length. In some
variations of the second reference arrangement, the bypass passage 180 may have other
cross-sectional profiles, such as oval shaped or polygonal shaped profiles. Further,
in some variations of the second reference arrangement, the cross sectional profile
and the diameter (or hydraulic diameter) of the bypass passage 180 may vary along
its longitudinal axis.
[0113] The provision of a bypass passage 180 means that a part of the air drawn through
the smoking substitute apparatus 150a when a user inhales via the mouthpiece 154 is
not drawn through the vaporisation chamber. This has the effect of reducing the flow
rate through the vaporisation chamber in correspondence with the respective flow resistances
presented by the vaporiser passage 170 and the bypass passage 180. This can reduce
the correlation between the flow rate through the smoking substitute apparatus 150a
(i.e. the user's draw rate) and the particle size generated when the e-liquid 160
is vaporised and subsequently forms an aerosol. Therefore, the smoking substitute
apparatus 150a of the second reference arrangement can deliver a more consistent aerosol
to a user.
[0114] Furthermore, the smoking substitute apparatus 150a of the second reference arrangement
is capable of producing an increased particle droplet size, dso, based on typical
inhalation rates undertaken by a user, compared to the first reference arrangement
of Figure 3. Such larger droplet sizes may be beneficial for the delivery of vapour
to a user's lungs. The preferred ratio between the dimensions of the bypass passage
180 and the dimensions of the vaporiser passage 170, and hence flow rate in the respective
passages may be determined from representative user inhalation rates and from the
required air flow rate through the vaporisation chamber to deliver a desired droplet
size. For example, an average total flow rate of 1.3 litres per minute may be split
such that 0.8 litres per minute passes through the bypass air channel 180, and 0.5
litres per minute passes through the vaporiser channel 170, a bypass:vaporiser flow
rate ratio of 1.6:1. Such a flow rate may provide an average droplet size, dso, of
1-3 µm (more preferably 2-3 µm) with a span of not more than 20 (preferably not more
than 10). Alternative flow rate ratios may be provided based on calculations and measurements
of user flow rate, vaporiser flow rate, and average droplet size dso. A bypass:vaporiser
flow rate ratio of between 0.5:1 and 20:1, typically at an average total flow rate
of 1.3 litres per minute may be advantageous depending on the configuration of the
smoking substitute apparatus.
[0115] The bypass passage and vaporiser passage extend from a common device inlet 176. This
has the benefit of ensuring more consistent airflow through the bypass passage 180
and vaporiser passage 170 across the lifetime of the smoking substitute apparatus
150a, since any obstruction that impinges on an air inlet 176 will affect the airflow
through both passages equally. The impact of inlet manufacturing variations can also
be reduced for the same reason. This can therefore improve the user experience for
the smoking substitute apparatus 150a. Furthermore, the provision of a common device
inlet 176 simplifies the construction and external appearance of the device.
[0116] The bypass passage 180 and vaporiser passage 170 separate upstream of the vaporisation
chamber. Therefore, no vapour is drawn through the bypass passage 180. Furthermore,
because the bypass passage leads to outlet 184 that is separate from outlet 174 of
the vaporiser passage, substantially no mixing of the bypass air and vaporiser air
occurs within the smoking substitute apparatus 150a. Such mixing could otherwise lead
to excessive cooling of the vapour and hence a build-up of condensation within the
smoking substitute apparatus 150a. Such condensation could have adverse implications
for delivering vapour to the user, for example by causing the user to draw liquid
droplets rather than vapour when "puffing" on the mouthpiece 154.
[0117] A further example of a bypass air flow is presented by a third reference arrangement.
Accordingly, in some embodiments, the apparatus may include one or a combination of
features of a third reference arrangement (and variations thereof), shown schematically
in Figure 6, where such features are combinable with the present invention. This third
reference arrangement is described below.
[0118] Figure 6 illustrates a longitudinal cross sectional view of a consumable 250 according
to a further arrangement. In Figure 6, the consumable 250 is shown attached, at a
first end of the consumable 250, to the main body 120 of Figure 1 and Figure 2. More
specifically, the consumable 250 is configured to engage and disengage with the main
body 120 and is interchangeable with the first reference arrangement 150 as shown
in Figures 3 and 4. Furthermore, the consumable 250 is configured to interact with
the main body 120 in the same manner as the first reference arrangement 150 and the
user may operate the consumable 250 in the same manner as the first reference arrangement
150.
[0119] The consumable 250 comprises a housing. The consumable 250 comprises an aerosol generation
chamber 280 in the housing. As shown in Figure 6, the aerosol generation chamber 280
takes the form of an open ended container, or a cup, with a single chamber outlet
282 opened towards the outlet 274 of the consumable 250.
[0120] In the illustrated third reference arrangement, the housing has a plurality of air
inlets 272 defined or opened at the sidewall of the housing. An outlet 274 is defined
or opened at a second end of the consumable 250 that comprises a mouthpiece 254. A
pair of passages 270 each extend between the respective air inlets 272 and the outlet
274 to provide flow passage for an air flow 412 as a user puffs on the mouthpiece
254. The chamber outlet 282 is configured to be in fluid communication with the passages
270. The passages 270 extend from the air inlets 272 towards the first end of the
consumable 250 before routing back to towards the outlet 274 at the second end of
the consumable 250. That is, a portion of each of the passages 270 axially extends
alongside the aerosol generation chamber 280. The path of the air flow path 412 is
illustrated in Figure 6. In variations of the third reference arrangement, the passages
270 may extend from the air inlet 272 directly to the outlet 274 without routing towards
the first end of consumable 250, e.g. the passages 270 may not axially extend alongside
the aerosol generation chamber 280.
[0121] In some other variations of the third reference arrangement, the housing may not
be provided with any air inlet for an air flow to enter the housing. For example,
the chamber outlet may be directly connected to the outlet of the housing by an aerosol
passage and therefore said aerosol passage may only convey aerosol as generated in
the aerosol generation chamber. In these variations, the discharge of aerosol may
be driven at least in part by the pressure increase during vaporisation of aerosol
form.
[0122] Referring back to the third reference arrangement of Figure 6, the chamber outlet
282 is positioned downstream from the heater in the direction of the vapour and/or
aerosol flow 414 and serves as the only gas flow passage to the internal volume of
the aerosol generation chamber 280. In other words, the aerosol generation chamber
280 is sealed against air flow except for having the chamber outlet 282 in communication
with the passages 270, the chamber outlet 282 permitting, in use, aerosol generated
by the heater to be entrained into an air flow along the passage 270. In some other
variations of the third reference arrangement, the sealed aerosol generation chamber
280 may comprise a plurality of chamber outlets 282 each arranged in fluid commutation
with the passages 270. In the illustrated third reference arrangement, the aerosol
generation chamber 280 does not comprise any aperture upstream of the heater that
may serve as an air flow inlet (although in some arrangements a vent may be provided).
In contrast with the consumable 150 as shown in Figures 3 and 4, the passages 270
of the consumable 250 allow the air flow, e.g. an entire amount of air flow, entering
the housing to bypass the aerosol generation chamber 280. Such arrangement allows
aerosol precursor to be vaporised in absence of the air flow. Therefore, the aerosol
generation chamber may be considered to be a "stagnant" chamber. For example, the
volumetric flowrate of vapour and/or aerosol in the aerosol generation chamber is
configured to be less than 0.1 litre per minute. The vaporised aerosol precursor may
cool and therefore condense to form an aerosol in the aerosol generation chamber 280,
which is subsequently expulsed into or entrained with the air flow in passages 270.
In addition, a portion of the vaporised aerosol precursor may remain as a vapour before
leaving the aerosol generation chamber 280, and subsequently forms an aerosol as it
is cooled by the air flow in the passages 270. The flow path of the vapour and/or
aerosol 414 is illustrated in Figure 6.
[0123] In the illustrated third reference arrangement, the chamber outlet 282 is configured
to be in fluid communication with a junction 290 at each of the passages 270 through
a respective vapour channel 292. The junctions 290 merge the vapour channels 292 with
their respective passages 270 such that vapour and/or aerosol formed in the aerosol
generation chamber 280 may expand or entrain into the passages 270 through junction
inlets of said junctions 290. The vapour channels form a buffering volume to minimise
the amount of air flow that may back flow into the aerosol generation chamber 280.
In some other variations of the third reference arrangement (not illustrated), the
chamber outlet 282 may directly open towards the junction 290 at the passage, and
therefore in such variations the vapour channel 292 may be omitted.
[0124] In some variations of the third reference arrangement (not illustrated), the chamber
outlet may be closed by a one way valve. Said one way valve may be configured to allow
a one way flow passage for the vapour and/or aerosol to be discharged from the aerosol
generation chamber, and to reduce or prevent the air flow in the passages from entering
the aerosol generation chamber.
[0125] In the illustrated third reference arrangement, the aerosol generation chamber 280
is configured to have a length of 20mm and a volume of 680mm
3. The aerosol generation chamber is configured to allow vapour to be expulsed through
the chamber outlet at a rate greater than 0.1mg/second. In other variations of the
third reference arrangement the aerosol generation chamber may be configured to have
an internal volume ranging between 68mm
3 to 680mm3, wherein the length of the aerosol generation chamber may range between
2mm to 20mm.
[0126] As shown in Figure 6, a part of each of the passages 270 axially extends alongside
the aerosol generation chamber 280. For example, the passages 270 are formed between
the aerosol generation chamber 280 and the housing. Such an arrangement reduces heat
transfer from the aerosol generation chamber 280 to the external surfaces of the housing.
[0127] The aerosol generation chamber 280 comprises a heater extending across its width.
The heater comprises a porous wick 262 and a heating filament 264 helically wound
around a portion of the porous wick 162. A tank 252 is provided in the space between
the aerosol generation chamber 280 and the outlet 274, the tank being for storing
a reservoir of aerosol precursor. Therefore in contrast with the reference arrangement
as shown in Figures 3 and 4, the tank 252 in the third reference arrangement does
not substantially surround the aerosol generation chamber nor the passage 270. Instead,
as shown in Figure 6, the tank is substantially positioned above the aerosol generation
chamber 280 and the porous wick 262 when the consumable 250 is placed in an upright
orientation during use. The end portions of the porous wick 262 each extend through
the sidewalls of the aerosol generation chamber 280 and into a respective liquid conduit
266 which is in fluid communication with the tank 252. The wick 262, saturated with
aerosol precursor, may prevent gas flow passage into the liquid conduits 266 and the
tank 252. Such an arrangement may allow the aerosol precursor stored in the tank 252
to convey towards the porous wick 262 through the liquid conduits 266 by gravity.
The liquid conduits 266 are configured to have a hydraulic diameter that allow a controlled
amount of aerosol precursor to flow from the tank 252 towards the porous wick 262.
More specifically, the size of liquid conduits 266 are selected based on the rate
of aerosol precursor consumption during vaporisation. For example, the liquid conduits
266 are sized to allow a sufficient amount of aerosol precursor to flow towards and
replenish the wick, yet not so large as to cause excessive aerosol precursor to leak
into the aerosol generation chamber. The liquid conduits 266 are configured to have
a hydraulic diameter ranging from 0.01 mm to 10mm or 0.01 mm to 5mm. Preferably, the
liquid conduits 266 are configured to have a hydraulic diameter in the range of 0.1mm
to 1mm.
[0128] The heating filament is electrically connected to electrical contacts 256 at the
base of the aerosol generation chamber 280, sealed to prevent air ingress or fluid
leakage. As shown in Figure 6, when the first end of the consumable 250 is received
into the main body 120, the electrical contacts 256 establish electrical communication
with corresponding electrical contacts of the main body 120, and thereby allow the
heater to be energised.
[0129] The vaporised aerosol precursor, or aerosol in the condensed form, may discharge
from the aerosol generation chamber 280 based on pressure difference between the aerosol
generation chamber 280 and the passages 270. Such pressure difference may arise form
i) an increased pressure in the aerosol generation chamber 280 during vaporisation
of aerosol form, and/or ii) a reduced pressure in the passage during a puff.
[0130] For example, when the heater is energised and forms a vapour, it expands in to the
stagnant cavity of the aerosol generation chamber 280 and thereby causes an increase
in internal pressure therein. The vaporised aerosol precursor may immediately begin
to cool and may form aerosol droplets. Such increase in internal pressure causes convection
inside the aerosol generation chamber which aids expulsing aerosol through the chamber
outlet 282 and into the passages 270.
[0131] In the illustrated third reference arrangement, the heater is positioned within the
stagnant cavity of the aerosol generation chamber 280, e.g. the heater is spaced from
the chamber outlet 282. Such arrangement may reduce or prevent the amount of air flow
entering the aerosol generation chamber, and therefore it may minimise the amount
of turbulence in the vicinity of the heater. Furthermore, such arrangement may increase
the residence time of vapour in the stagnant aerosol generation chamber 280, and thereby
may result in the formation of larger aerosol droplets. In some other variations of
the third reference arrangement, the heater may be positioned adjacent to the chamber
outlet and therefore that the path of vapour 414 from the heater to the chamber outlet
282 is shortened. This may allow vapour to be drawn into or entrained with the air
flow in a more efficient manner.
[0132] The junction inlet at each of the junctions 290 opens in a direction orthogonal or
non-parallel to the air flow. That is, the junction inlet each opens at a sidewall
of the respective passages 270. This allows the vapour and/or aerosol from the aerosol
generation chamber 280 to entrain into the air flow at an angle, and thus improving
localised mixing of the different streams, as well as encouraging aerosol formation.
The aerosol may be fully formed in the air flow and be drawn out through the outlet
at the mouthpiece.
[0133] With the absence of, or much reduced, air flow in the aerosol generation chamber,
the aerosol as generated by the illustrated third reference arrangement has a median
droplet size dso of at least 1µm. More preferably, the aerosol as generated by the
illustrated third reference arrangement has a median droplet size dso of ranged between
2µm to 3µm.
[0134] The present invention is an improvement, not illustrated in Figures 1-6, that can
be applied to each of the described reference arrangements (and of course to many
more). Each of their features can therefore be understood as, in effect, features
of embodiments of the present invention.. The present invention is schematically illustrated
in Figures 7A and 7B, although it will be appreciated that the geometry of the described
components may be varied to fit with the other parts of the device to which the present
invention is applied. For simplicity, it is illustrated in a device similar to that
of the reference arrangements illustrated in Figures 3, 4 and 5.
[0135] In view of that, parts of the embodiment illustrated in Figures 7A and 7B corresponding
to parts of the reference arrangements illustrated in Figures 3, 4 and 5 will be given
the same reference numerals as in Figures 3, 4 and 5, suffixed with 'A'.
[0136] In the present invention, there is provided an expandable absorbent body which, in
its unexpanded form, is separated from the wick via an air gap and wherein the expandable
absorbent body, in its expanded form, is configured to contact the wick. This expandable
absorbent body is positioned and adapted to 'catch' (i.e. absorb) vapourisable liquid
which escapes or leaks from the tank without being transported by the wick for vaporisation,
or which leaks from the wick itself. Because of the air gap separating it from the
wick in its unexpanded form, it does not leach liquid from the wick or tank in a normal
use case. In general the absorbent body is made from an absorbent material, and the
terms can be used interchangeably.
[0137] In the absorbent body's unexpanded form, it simply absorbs leaked liquid. This provides
an advantage in that said liquid does not leak further into (or even out of) the smoking
substitute apparatus.
[0138] Ideally, the absorbent body expands as it absorbs more and more liquid. That is,
it gradually transforms from its unexpanded for to its expanded form (i.e. it gradually
expands) by absorption of liquid.
[0139] Once in its expanded form, the absorbent body contacts the wick. This forms a fluid
pathway by which liquid in the absorbent body can be drawn into the wick by the same
capillary action by which liquid from the tank is drawn into the wick (and hence to
the vaporization chamber for vaporization). Accordingly at least some of the liquid
which would otherwise have been lost or wasted can be used, improving the efficiency
of the device.
[0140] It can be understood that the absorbent body has an empty configuration, in which
it has absorbent zero liquid (0% expanded), and a maximally expanded configuration,
in which it has reached its absorption capacity and hence has expanded as much as
it can through liquid absorption (100% expanded). In this configuration it has reached
full absorbent capacity and cannot absorb any more liquid.
[0141] The expanded form of the absorbent body, in which it comes into contact with the
wick, is not necessarily the same as the maximum possible expansion of the body. Indeed
it is preferable that the absorbent body is designed such that its full absorbent
capacity is not reached in normal circumstances, as at that capacity leakage of the
type the body is intended to avoid may occur.
[0142] It may be preferable in some embodiments for the expanded form to be equivalent to
a relatively high level of expansion, for example in arrangements where a significant
level of leakage is expected (and hence where high expansion of the body can be expected,
ensuring usage of the absorbs liquid). For example, the expanded form may be equivalent
to an expansion which is at least 50% of the maximum expansion, for example at least
60%, at least 70% or at least 80% of the maximum expansion.
[0143] On the other hand, in other embodiments it may be preferable for the expanded form
to be equivalent to a relatively low level of expansion, for example in arrangements
where a relatively small level of leakage is expected (and hence where low expansion
of the body can be expected; in order to use the absorbed liquid, then, such allow
expansion needs to be sufficient to induce contact between the absorbent body and
the wick). For example, the expanded form may be equivalent to an expansion which
is at most 50% of the maximum expansion, for example at most 40%, at most 30% or at
most 20% of the maximum expansion.
[0144] Turning to Figures 7A and 7B, in which an embodiment of the invention is schematically
illustrated in cross section: Figure 7A shows the unexpanded form and Figure 7B shows
the expanded form.
[0145] In Figures 7A, the absorbent body 500 is located in a cavity 502 formed separate
from the tank 152a which contains the e-liquid 160a. The cavity 502 is sealed from
that tank by the wick 162a. In a normal operation mode, liquid 160a is drawn into
the wick 162a by capillary action, indicated by arrows 401a. Air flows into the vaporization
chamber (arrow 402a), where as explained above it entrains vapour generated by the
wick. It then flows onward, arrow 403a, to a flow passage 170a which leads to the
outlet and ultimately to the user.
[0146] An air gap 503 separates the absorbent body 500 from the wick 162a. This gap means
that there is not direct absorption of liquid 160a by the absorbent body 500 from
the tank 152a, which would somewhat defeat the object of the absorbent body 500.
[0147] The cavity 502 and preferably also the absorbent body 500 may for example provided
with an annular cross section (that is, it is an annular cylinder), surrounding the
flow passage upstream of the wick 162a. It may be that the interior wall of the cavity
502 defines the wall of that flow passage. However it will be recognised that the
shape of the absorbent body and the cavity may vary significantly depending on the
geometry of the smoking substitute apparatus or vapour generating system in which
they will be located.
[0148] The shape and location of the cavity and absorbent body may also be adapted depending
on the location of likely leakage points. For example, it may be that two cavities
and absorbent bodies are needed, to catch leaks from the tank/wick interfaces.
[0149] In some embodiments, the cavity 502 may be filled in at least one dimension by the
absorbent body 500. This can act to encourage or even force expansion of the absorbent
body 500 in the other dimensions. Most preferably, the absorbent body is sized to
fill the cavity 502 in all but one direction, thus inducing maximum expansion in that
direction. Suitably that direction is towards the wick 162a.
[0150] In order to more effectively catch liquid which leaks or is otherwise lost from the
tank 152a or the wick 162a, the cavity 502 and hence the absorbent body 500 may be
provided at a location which is gravitationally below the tank 152a and/or the wick
162a when the vapour generating system of the present invention is in normal use.
This means that, in normal use, leaked liquid will be carried to the absorbent body
by the action of gravity, making the absorption more efficient.
[0151] In Figure 7B there is illustrated the situation after some period of usage, and hence
some leakage of liquid into the cavity 502 and thus the absorbent body 500 has occurred.
The level of liquid 160a in the tank 152a has reduced. The absorbent body 500 has
expanded (it is in its expanded form), and contacts the wick 162a. Air gap 503 has
now gone, filled by the expanding absorbent body 500.
[0152] In this expanded form, the absorbent body 500 contacts the wick 162a. In particular
it contacts the wick at is two longitudinal ends; those ends are also in contact with
the tank 152a. Accordingly, liquid 160a absorbed by the absorbent body 500 can be
drawn into the wick 162a by capillary action (indicated by arrows 501), supplementing
the supply of liquid 160a from the tank 152a by capillary action 401a.
[0153] It will be recognised that, in general, the tank 152a provides direct liquid contact
between the liquid 160a and the wick 162a. Accordingly it may be that capillary transport
from the tank into and through the wick 162a encounters a lower force boundary than
capillary transport from the absorbent body 500 into and through the wick 162a. This
means that liquid is preferentially drawn from the tank 152a instead of from the absorbent
body 500 when both routes are available (i.e. when the absorbent body 500 is in its
expanded form and contacts the wick 162a).
[0154] However it can be envisaged that the absorbent body 500 is chosen and adapted such
that liquid is preferentially drawn from it, rather than from the tank 152a, when
both routes are available.
[0155] When all the liquid 160a in the tank 152a is used, the capillary supply 501 from
the absorbent body 500 may be the sole source of liquid 160a for the wick 162a.
[0156] The present invention also relates to the use of a vapour generating system as described
herein. Such a use may comprise an initial operation mode, which occurs for example
when the system is first engaged/used, and a subsequent operation mode, which occurs
for example after the system has been in use for some time (not necessarily in a single
session also including the initial operation mode). In the initial operation of the
system, the reservoir retains the vaporisable liquid and the wick absorbs vaporisable
liquid from the reservoir, and the heater vaporises the vaporisable liquid absorbed
by the wick, the expandable absorbent body being separated from the wick via said
air gap. It is this separation that characterises the initial operation of the system;
in that operation, due to the air gap, the wick does not (as explained above) draw
liquid from the absorbent body. It cannot do so. On the other hand, in the subsequent
operation of the system, that is not the case. As explained above, during use the
expandable absorbent body gradually captures liquid lost from the reservoir and/or
wick and expands so that, in the subsequent operation of the system, the expandable
absorbent body contacts the wick to allow liquid in the expandable absorbent body
to move into the wick for vaporisation.
[0157] The features disclosed in the foregoing description, or in the following claims,
or in the accompanying drawings, expressed in their specific forms or in terms of
a means for performing the disclosed function, or a method or process for obtaining
the disclosed results, as appropriate, may, separately, or in any combination of such
features, be utilised for realising the invention in diverse forms thereof.
[0158] While the invention has been described in conjunction with the exemplary embodiments
described above, many equivalent modifications and variations will be apparent to
those skilled in the art when given this disclosure. Accordingly, the exemplary embodiments
of the invention set forth above are considered to be illustrative and not limiting.
Various changes to the described embodiments may be made without departing from the
spirit and scope of the invention.
[0159] For the avoidance of any doubt, any theoretical explanations provided herein are
provided for the purposes of improving the understanding of a reader. The inventors
do not wish to be bound by any of these theoretical explanations.
[0160] Any section headings used herein are for organizational purposes only and are not
to be construed as limiting the subject matter described.
[0161] Throughout this specification, including the claims which follow, unless the context
requires otherwise, the words "have", "comprise", and "include", and variations such
as "having", "comprises", "comprising", and "including" will be understood to imply
the inclusion of a stated integer or step or group of integers or steps but not the
exclusion of any other integer or step or group of integers or steps.
[0162] It must be noted that, as used in the specification and the appended claims, the
singular forms "a," "an," and "the" include plural referents unless the context clearly
dictates otherwise. Ranges may be expressed herein as from "about" one particular
value, and/or to "about" another particular value. When such a range is expressed,
another embodiment includes from the one particular value and/or to the other particular
value. Similarly, when values are expressed as approximations, by the use of the antecedent
"about," it will be understood that the particular value forms another embodiment.
The term "about" in relation to a numerical value is optional and means, for example,
+/- 10%.
[0163] The words "preferred" and "preferably" are used herein refer to embodiments of the
invention that may provide certain benefits under some circumstances. It is to be
appreciated, however, that other embodiments may also be preferred under the same
or different circumstances. The recitation of one or more preferred embodiments therefore
does not mean or imply that other embodiments are not useful, and is not intended
to exclude other embodiments from the scope of the disclosure, or from the scope of
the claims.