Technical field
[0001] The present disclosure relates to an aerosol delivery system such as a smoking substitute
system.
Background
[0002] The smoking of tobacco is generally considered to expose a smoker to potentially
harmful substances. It is generally thought that a significant amount of the potentially
harmful substances are generated through the heat caused by the burning and/or combustion
of the tobacco and the constituents of the burnt tobacco in the tobacco smoke itself.
[0003] 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 order to avoid the smoking of tobacco.
[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] Smoking substitute systems, which may also be known as electronic nicotine delivery
systems, may comprise electronic systems that permit a user to simulate the act of
smoking by producing an aerosol, also referred to as a "vapour", which is drawn into
the lungs through the mouth (inhaled) and then exhaled. The inhaled aerosol typically
bears nicotine and/or flavourings without, or with fewer of, the odour and health
risks associated with traditional 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 experience and satisfaction
to those experienced with traditional smoking and tobacco products.
[0007] The popularity and use of smoking substitute systems has grown rapidly in the past
few years. Although originally marketed as an aid to assist habitual smokers wishing
to quit tobacco smoking, consumers are increasingly viewing smoking substitute systems
as desirable lifestyle accessories. Some smoking substitute systems are designed to
resemble a traditional cigarette and are cylindrical in form with a mouthpiece at
one end. Other smoking substitute systems do not generally resemble a cigarette (for
example, the smoking substitute device may have a generally box-like form).
[0008] There are a number of different categories of smoking substitute systems, each utilising
a different smoking substitute approach. A smoking substitute approach corresponds
to the manner in which the substitute system operates for a user.
[0009] One approach for a smoking substitute system is the so-called "vaping" approach,
in which a vaporisable liquid, typically referred to (and referred to herein) as "e-liquid",
is heated by a heater to produce an aerosol vapour which is inhaled by a user. An
e-liquid typically includes a base liquid as well as nicotine and/or flavourings.
The resulting vapour therefore typically contains nicotine and/or flavourings. The
base liquid may include propylene glycol and/or vegetable glycerine.
[0010] A typical vaping smoking substitute system includes a mouthpiece, a power source
(typically a battery), a tank or liquid reservoir for containing e-liquid, as well
as a heater. In use, electrical energy is supplied from the power source to the heater,
which heats the e-liquid to produce an aerosol (or "vapour") which is inhaled by a
user through the mouthpiece.
[0011] Vaping smoking substitute systems can be configured in a variety of ways. For example,
there are "closed system" vaping smoking substitute systems which typically have a
heater and a sealed tank which is pre-filled 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 device which includes the power source, wherein the device is configured
to be physically and electrically coupled to a component including the tank and the
heater. In this way, when the tank of a component has been emptied, the device can
be reused by connecting it to a new component. Another subset of closed system vaping
smoking substitute systems are completely disposable and intended for one-use only.
[0012] There are also "open system" vaping smoking substitute systems which typically have
a tank that is configured to be refilled by a user, so the system can be used multiple
times.
[0013] An example vaping smoking substitute system is the myblu
™ e-cigarette. The myblu
™ e cigarette is a closed system which includes a device and a consumable component.
The device and consumable component are physically and electrically coupled together
by pushing the consumable component into the device. The device includes a rechargeable
battery. The consumable component includes a mouthpiece, a sealed tank which contains
e-liquid, as well as a vaporiser, which for this system is a heating filament coiled
around a portion of a wick which is partially immersed in the e-liquid. The system
is activated when a microprocessor on board the device detects a user inhaling through
the mouthpiece. When the system is activated, electrical energy is supplied from the
power source to the vaporiser, which heats e-liquid from the tank to produce a vapour
which is inhaled by a user through the mouthpiece.
[0014] Another example vaping smoking substitute system is the blu PRO
™ e-cigarette. The blu PRO
™ e cigarette is an open system which includes a device, a (refillable) tank, and a
mouthpiece. The device and tank are physically and electrically coupled together by
screwing one to the other. The mouthpiece and refillable tank are physically coupled
together by screwing one into the other, and detaching the mouthpiece from the refillable
tank allows the tank to be refilled with e-liquid. The system is activated by a button
on the device. When the system is activated, electrical energy is supplied from the
power source to a vaporiser, which heats e-liquid from the tank to produce a vapour
which is inhaled by a user through the mouthpiece.
[0015] An alternative to the "vaping" approach is the so-called Heated Tobacco ("HT") approach
in which tobacco (rather than an e-liquid) is heated or warmed to release vapour.
HT is also known as "heat not burn" ("HNB"). The tobacco may be leaf tobacco or reconstituted
tobacco. In the HT approach the intention is that the tobacco is heated but not burned,
i.e. the tobacco does not undergo combustion.
[0016] The heating, as opposed to burning, of the tobacco material is believed to cause
fewer, or smaller quantities, of the more harmful compounds ordinarily produced during
smoking. Consequently, the HT approach may reduce the odour and/or health risks that
can arise through the burning, combustion and pyrolytic degradation of tobacco.
[0017] A typical HT smoking substitute system may include a device and a consumable component.
The consumable component may include the tobacco material. The device and consumable
component may be configured to be physically coupled together. In use, heat may be
imparted to the tobacco material by a heating element of the device, wherein airflow
through the tobacco material causes components in the tobacco material to be released
as vapour. A vapour may also be formed from a carrier in the tobacco material (this
carrier may for example include propylene glycol and/or vegetable glycerine) and additionally
volatile compounds released from the tobacco. The released vapour may be entrained
in the airflow drawn through the tobacco.
[0018] As the vapour passes through the consumable component (entrained in the airflow)
from the location of vaporization to an outlet of the component (e.g. a mouthpiece),
the vapour cools and condenses to form an aerosol for inhalation by the user. The
aerosol may contain nicotine and/or flavour compounds.
[0019] Upon exhalation, nicotine, flavor components and other components that have not been
deposited in the lungs or lost in the respiratory tract leave the body and enter the
ambient air. This is undesirable for the several reasons. For example, it poses the
risk of passive 'smoking' to others. Specifically, it risks the inhalation of the
second-hand vapour by others, thus risking the intake of nicotine or other potentially
harmful substances by those who do not specifically intend or wish to intake them.
This is especially problematic in confined spaces and/or around children or those
with a health condition, for which the nicotine or other components may be particularly
harmful. However, passive 'smoking' is considered undesirable by many non-users of
cigarettes or smoking substitute devices, regardless of their age or health status.
The exhalation of vapour from smoking substitute systems can therefore cause social
difficulty for the user.
[0020] Moreover, there are rules and laws in many jurisdictions that include public bans
on smoking, which extend to a ban on vaping and the use of smoking substitutes in
some jurisdictions. The rationale behind such rules and laws is typically based on
the potential risk that smoking and vaping pose to others via passive smoking.
[0021] Accordingly, there is a need for an improved aerosol delivery device/system which
addresses at least some of the problems of the known devices and systems.
Summary
[0022] According to a first aspect, there is provided an aerosol generating system comprising:
aerosol generating means configured to generate an aerosol for delivery to a user
during inhalation;
a mouthpiece for exhalation of air into the system;
a filter configured to filter exhaled air entering the system through the mouthpiece
during a user exhalation, wherein a bypass channel is configured to direct exhaled
air to the filter whilst bypassing the aerosol generating means;
one or more exhalation airflow sensors configured to detect an airflow property of
exhaled air passing through the filter; and
a controller configured to determine a state of the filter based on the detected airflow
property of exhaled air.
[0023] By monitoring a property of the exhaled air passing through the filter, the aerosol
generating system is configured to monitor (i.e., sense, detect, or measure) a property
that provides an accurate indicator of the instantaneous state of the filter. One
or more exhalation airflow sensors such as conventional airflow sensors may be employed
for this purpose, such that the monitoring does not require costly, complex or bulky
component parts to be incorporated into the aerosol generating system. However, the
present inventors have recognised that, by intelligently locating the one or more
sensors so that they can detect an airflow rate of exhaled air passing through the
filter, those sensors can provide highly useful information regarding the state of
the filter and therefore can provide the user with accurate and dynamic information
to ensure that the filtration of exhaled air that the system is providing is always
sufficiently high standard. As a result, the user can ensure but they are using a
suitable filter at all times, which will enable the system to clean and purify the
exhaled air as it passes through the system, before it is exhaled into the surrounding
environment. Therefore, the user can ensure that the system is not outputting any
remnant vapour or other contaminants that could adversely affect other people in the
vicinity, should those other people inhale the airstream that the aerosol generating
system outputs. Therefore, the overall safety, reliability, and social acceptability
of using an aerosol generating system such as a smoking substitute system is improved.
[0024] Optional features will now be set out. These are applicable singly or in any combination
with any aspect.
[0025] The aerosol generating means (also referred to herein as the "vaporiser") may be
configured to generate the aerosol for delivery to the user via the mouthpiece during
the user inhalation i.e. the mouthpiece may be for both inhalation of vapour/aerosol
from the system and exhalation of exhaled air into the system.
[0026] The exhalation airflow sensor(s) may, for example, be in the form of a pressure sensor
or an acoustic sensor.
[0027] At least one of the one or more exhalation airflow sensors may be provided in the
bypass channel and/or in the filter.
[0028] The system may comprise an exhalation port extending from the filter to the exterior
of the system. Accordingly, an exhalation pathway may extend from the mouth piece,
through the bypass channel to the filter and from the filter to the exterior of the
system via with exhalation port.
[0029] At least one of the one or more exhalation airflow sensors may be provided in the
exhalation port.
[0030] The filter may removably connectable within the system. The filter may be provided
in a filter chamber or cavity. The filter cavity or chamber may have an opening e.g.
a sealable opening through which the filter can be removed and replaced.
[0031] The filter may comprise a porous filter material which may be fibrous material, a
meshed material or may be porous network. For example the porous filter material may
comprise cellulose acetate tow.
[0032] The system may further comprise a one-way valve that is configured to prevent the
flow of exhaled air from the mouthpiece to the aerosol generating means. The one-way
valve may be provided in or close to the mouthpiece. The one-way valve may be configured
to direct the exhaled air into or through the bypass channel.
[0033] The one or more exhalation airflow sensors may be configured to detect one or more
properties of the exhaled air selected from the airflow rate, pressure or volume through
the filter.
[0034] Additionally/alternatively, the one or more exhalation airflow sensors may be configured
to detect one or more properties selected from a drop in air flow rate, pressure or
volume across the filter. For example, a first exhalation airflow sensor may be provided
in the bypass channel upstream of the filter and a second exhalation airflow sensor
may be provided in the exhalation port downstream of the filter and the controller
may be configured to calculate a difference in values between the first and second
exhalation airflow sensors to calculate a drop of the airflow rate, pressure or volume
of the exhaled air across the filter.
[0035] The controller may be configured to determine a saturation level of the filter based
on the detected airflow property. In general terms, a filter that is saturated or
approaching saturation may act as a (partial) barrier to the flow of exhaled air and
therefore may decrease the flow rate, pressure or volume of the exhaled air.
[0036] The controller may be configured to determine that the filter should be replaced
based on the detected airflow parameter. If the controller determines that the filter
is saturated or approaching saturation, based on the detected parameter, it may determine
that it is appropriate for the filter to be changed in order to ensure a high level
of reliability of the filtration that the aerosol generating system is configured
to provide, on an ongoing basis.
[0037] The controller may be configured to determine that the filter should be replaced
by comparing the detected exhaled airflow property with a predefined threshold. The
predefined, or predetermined, threshold may comprise a minimum acceptable flow rate/pressure/volume
of exhaled air across the filter. If the exhaled air is flowing at a flow rate/pressure/volume
that is less than the predefined threshold, the controller may determine that the
filter is saturated or becoming saturated and therefore presenting an unacceptably
significant (or, unacceptably impenetrable) barrier for the exhaled air to pass through,
such that the filter should be replaced. In a similar manner, if the controller determines
that the drop in rate/pressure/volume of the exhaled air across the filter exceeds
a predefined threshold, replacement of the filter may be indicated.
[0038] By determining that the filter should be replaced, the controller is configured to
pre-empt and therefore prevent problems that may otherwise occur if a saturated filter
was allowed to remain in the system for too long. For example, a saturated filter
may allow some or all of the exhalation airflow to pass by the filter without being
sufficiently cleaned or purified by the filter.
[0039] The controller may be configured to output an alert based on determined state of
the filter e.g. if the filter is deemed to be at or approaching saturation. The alert
may be output via a feedback means within the system and/or via a remote device that
is communicatively connected to the controller. The alert may be a visual alert and/or
an audible alert and/or a haptic alert.
[0040] The system may comprise an aerosol delivery device and a component for containing
an aerosol precursor. The filter may be (removably) provided within the device. For
example, the device may comprise the filter chamber/cavity for receiving the filter.
Accordingly, the exhalation port may be provided in the device.
[0041] The device comprises a source of power which may be a battery. The source of power
may be a capacitor. The power source may be a rechargeable power source. The device
may comprise a charging connection for connection to an external power supply for
recharging of the power source within the device.
[0042] The device may comprise a device body for housing the power source and/or other electrical
components. The device body may be an elongate body i.e. with a greater length than
depth/width. It may have a greater width than depth.
[0043] The device body may have a length of between 5 and 30 cm e.g. between 5 and 10 cm
such as between 7 and 9 cm. The maximum depth of the device body may be between 5
and 15 mm e.g. between 9 and 12 mm.
[0044] The device body may have a front surface that is curved in the transverse dimension.
The device body may have a rear surface that is curved in the transverse dimension.
The curvatures of the front surface and rear surface may be of the opposite sense
to one another. Both front and rear surfaces may be convex in the transverse dimension.
They may have an equal radius of curvature.
[0045] The device body may have a substantially oval transverse cross-sectional shape.
[0046] The device body may have a linear longitudinal axis.
[0047] The front and/or rear surface of the device body may include at least one visual
user feedback element, for example one or more lights e.g. one or more LEDs. These
may be configured to provide the user alert, based on the determined state of the
filter.
[0048] In some embodiments, the device body may include an illumination region configured
to allow light provided by the visual user feedback element (e.g. one or more lights/LEDs)
within the device body to shine through.
[0049] The device may comprise a movement detection unit (e.g. an accelerometer) for detecting
a movement of the device.
[0050] The device may comprise a haptic feedback generation unit (e.g. an electric motor
and a weight mounted eccentrically on a shaft of the electric motor). The haptic feedback
generation unit may be configured to provide the user alert, based on the determined
state of the filter.
[0051] The device may include the controller.
[0052] The controller may be configured to identify an operation of the device; and control
the one or more lights contained within the device body, (e.g. to illuminate the illumination
region) based on the operation of the device identified.
[0053] The controller may be configured to control the haptic feedback generation unit to
generate the haptic feedback in response to the detection of movement of the device
by the movement detection unit.
[0054] 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.
The memory may store the predefined threshold, to which the airflow property of exhaled
air is compared, by the controller, for determining a state of the filter.
[0055] The device may comprise a wireless interface, which may be configured to communicate
wirelessly with anotherdevice, 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.
[0056] The device may comprise an inhalation airflow (i.e. puff) sensor that is configured
to detect a puff (i.e. inhalation from a user). The inhalation airflow 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
inhalation airflow sensor may, for example, be in the form of a pressure sensor or
an acoustic sensor.
[0057] The controller may control power supply to the aerosol generating means/vaporiser
in response to airflow detection by the inhalation airflow sensor. The control may
be in the form of activation of the vaporiser in response to a detected inhalation
airflow.
[0058] The device may comprise an electrical connection (e.g. one or more contact pins)
for connection of the power source to the vaporiser.
[0059] The device may comprise a chassis within the device body and one or more of the electrical
components of the device (e.g. one or more of the power source, charging connection,
visual feedback element, movement detection unit, haptic feedback generation unit,
controller, memory, wireless interface, inhalation airflow sensor, exhalation airflow
sensor(s) and/or electrical connection) may be mounted on or affixed to the chassis.
[0060] The component of the system may be an aerosol-delivery (e.g. a smoking substitute)
consumable i.e. in some embodiments the component may be a consumable component for
engagement with the aerosol-delivery (e.g. a smoking substitute) device to form the
aerosol-delivery (e.g. s smoking substitute) system.
[0061] The device may be configured to receive the consumable component. The device and
the consumable component may be configured to be physically coupled together. For
example, the consumable component may be at least partially received in a recess of
the device (e.g. in a recess defined by the device housing). There may be a snap engagement
between the device and the consumable component. Alternatively, the device and the
consumable component may be physically coupled together by screwing one onto the other,
or through a bayonet fitting.
[0062] Thus, the consumable component may comprise one or more engagement portions for engaging
with the device.
[0063] The device and consumable component may be coupled together by magnetic attraction.
For example, the device may comprise at least one magnet whilst the component may
comprise a magnet or ferrous plate.
[0064] The consumable component may comprise the aerosol generating means, hereinafter referred
to as the vaporiser. The vaporiser may comprise a heating element. Alternatively,
the vaporiser may comprise an ultrasonic or flow expansion unit, or an induction heating
system.
[0065] The consumable component may comprise an electrical interface for interfacing with
a corresponding electrical interface of the device. One or both of the electrical
interfaces may include one or more electrical contacts. Thus, when the device is engaged
with the consumable component, the electrical interface may be configured to transfer
electrical power from the power source to the vaporiser (e.g. heating element) of
the consumable component. The electrical interface may also be used to identify the
consumable component from a list of known types. The electrical interface may additionally
or alternatively be used to identify when the consumable component is connected to
the device.
[0066] The device may alternatively or additionally be able to detect information about
the consumable component via an RFID reader, a barcode or QR code reader. This interface
may be able to identify a characteristic (e.g. a type) of the consumable. In this
respect, the consumable component 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.
[0067] In other embodiments, the component may be integrally formed with the aerosol-delivery
(e.g. a smoking substitute) device to form the aerosol-delivery (e.g. s smoking substitute)
system.
[0068] In such embodiments, the aerosol former (e.g. e-liquid) may be replenished by re-filling
a tank that is integral with the device (rather than replacing the consumable). Access
to the tank (for re-filling of the e-liquid) may be provided via e.g. an opening to
the tank that is sealable with a closure (e.g. a cap).
[0069] The smoking substitute system may comprise an inhalation airflow path therethrough,
the inhalation airflow path extending from an air inlet to an outlet. The air inlet
may be provided in the device body. The outlet may be at the mouthpiece of the component.
In this respect, a user may draw fluid (e.g. air) into and along the inhalation airflow
path by inhaling at the outlet (e.g. using the mouthpiece).
[0070] The smoking substitute system may also comprise an exhalation airflow path that extends
from the mouthpiece to the filter via the bypass channel. It may then extend from
the filter to the exterior of the system via the exhalation port. The bypass channel
may separate the inhalation airflow path from the exhalation airflow path.
[0071] The inhalation airflow path passes the vaporiser between the air inlet and the outlet.
The vaporiser may be provided in the component. The exhalation airflow path bypasses
the vaporiser.
[0072] The inhalation airflow path may comprise a first portion extending from the air inlet
towards the vaporiser. A second portion of the inhalation airflow path passes the
vaporiser (e.g. over or around the vaporiser) to a conduit that extends to the outlet.
The conduit may extend along the axial centre of the component.
[0073] References to "downstream" in relation to the inhalation airflow path are intended
to refer to the direction towards the outlet/mouthpiece. Thus the second portion of
the inhalation airflow path is downstream of the first portion of the airflow path.
Conversely, references to "upstream" are intended to refer to the direction towards
the air inlet. Thus the first portion of the inhalation airflow path (and the air
inlet) is upstream of the second portion of the inhalation airflow path (and the outlet/mouthpiece).
[0074] References to "upper", "lower", "above" or "below" are intended to refer to the component
when in an upright/vertical orientation i.e. with elongate (longitudinal/length) axis
of the component vertically aligned and with the mouthpiece vertically uppermost.
[0075] The component may comprise a tank for housing the aerosol precursor (e.g. a liquid
aerosol precursor). The aerosol precursor may comprise an e-liquid, for example, comprising
a base liquid and e.g. nicotine. The base liquid may include propylene glycol and/or
vegetable glycerine.
[0076] The conduit may extend through the tank with the conduit walls defining an inner
region of the tank. In this respect, the tank may surround the conduit e.g. the tank
may be annular.
[0077] As discussed above, the inhalation airflow path passes (e.g. passes over or around)
the vaporiser between the air inlet and the outlet. The vaporiser may be within a
vaporiser chamber.
[0078] The vaporiser may comprise a wick. The wick may form the base of the tank so that
the aerosol precursor may be in contact with the wick. The wick may comprise one or
more channels on its upper surface (facing the tank), the channels being in fluid
communication with the tank.
[0079] The wick may have a length and width defining its upper surface with a depth aligned
with the longitudinal axis of the component. Thus the upper surface and opposing lower
surface of the wick may lie in respective planes that are perpendicular to the longitudinal
axis of component and longitudinal to the first and third portions of the airflow
path.
[0080] The wick may comprise a porous material e.g. a ceramic material. A portion of the
wick e.g. at least a portion of the lower surface and/or at least a portion of at
least one side wall extending between the upper and lower surface (in a depth direction)
may be exposed to airflow in the second portion of the inhalation airflow path.
[0081] The heating element may be in the form of a heater track on the wick e.g. on the
lower surface of the wick.
[0082] In other embodiments, the wick may be a cylindrical, porous wick e.g. formed of cotton
or ceramic. It may be oriented so as to extend in the direction of the width dimension
of the component (perpendicular to the longitudinal axis of the component). Thus the
wick may extend in a direction perpendicular to the direction of airflow in the airflow
path. Opposing ends of the wick may protrude into the tank and a central portion (between
the ends) may extend across the airflow path so as to be exposed to airflow. Thus,
fluid may be drawn (e.g. by capillary action) along the wick, from the tank to the
exposed portion of the wick. The heating element may be in the form of a filament
wound about the wick (e.g. the filament may extend helically about the wick). The
filament may be wound about the exposed portion of the wick.
[0083] The heating element is electrically connected (or connectable) to the power source.
Thus, in operation, the power source may supply electricity to (i.e. apply a voltage
across) the heating element so as to heat the heating element. This may cause liquid
stored in the wick (i.e. drawn from the tank) to be heated so as to form a vapour
and become entrained in airflow along the inhalation airflow path. This vapour may
subsequently cool to form an aerosol e.g. in the conduit.
[0084] In some embodiments, the filter may be provided in the component rather than the
device. In these embodiments, the component comprises the filter chamber and the at
least one exhalation air flow sensors. The exhalation port may extend from the filter
chamber to the exterior of the system entirely through the component or the exhalation
port may extend from the component through the device to the exterior of the system.
[0085] In some embodiments, the system further comprises a remote device that is communicatively
coupled to the aerosol generating system, wherein the controller of the aerosol generating
system is configured to output an alert to the remote device regarding a determined
state of the filter.
[0086] For example, the remote device may comprise a mobile device such as a mobile phone.
The remote device may be configured to run a software programme or software application
that is configured for communication with the controller.
[0087] According to a second aspect, a method is provided of monitoring the state of a filter
in an aerosol generating system according to said first aspect. The method comprises
detecting an airflow property of exhaled air passing through the filter; and determining
a state of the filter based on the detected airflow property of exhaled air. The method
may further comprise determining whether the filter should be replaced, based on the
detected airflow property. The method may further comprise issuing a user alert if
it has been determined that the filter should be replaced.
[0088] The method may be a computer-implemented method.
[0089] According to a third aspect, a computer-readable medium is provided containing instructions
configured to, when executed by a processor or by an application installed on a mobile
device, cause the processor or application to perform the method of the second aspect.
[0090] In a fourth aspect there is provided a method of using the aerosol-delivery (e.g.
smoking substitute) system according to the first aspect, the method comprising engaging
the consumable component with an aerosol-delivery (e.g. smoking substitute) device
(as described above) having a power source so as to electrically connect the power
source to the consumable component (i.e. to the vaporiser of the consumable component).
[0091] The invention includes the combination of the aspects and preferred features described
except where such a combination is clearly impermissible or expressly avoided.
BRIEF DESCRIPTION OF THE DRAWINGS
[0092] So that further aspects and features thereof may be appreciated, embodiments will
now be discussed in further detail with reference to the accompanying figures, in
which:
- Fig. 1A is a front schematic view of a smoking substitute system;
- Fig. 1B is a front schematic view of a device of the system;
- Fig. 1C is a front schematic view of a component of the system;
- Fig. 2A is a schematic of the electrical components of the device;
- Fig. 2B is a schematic of the parts of the component;
- Fig. 3 is a further schematic of the component having a filter;
- Fig. 4 is schematic of the device having a filter.
DETAILED DESCRIPTION OF THE EMBODIMENTS
[0093] Aspects and embodiments will now be discussed with reference to the accompanying
figures. Further aspects and embodiments will be apparent to those skilled in the
art.
[0094] Fig. 1A shows a first embodiment of a smoking substitute system 100. In this example,
the smoking substitute system 100 includes a device 102 and a component 104. The component
104 may alternatively be referred to as a "pod", "cartridge" or "cartomizer". It should
be appreciated that in other examples (i.e. open systems), the device may be integral
with the component. In such systems, a tank of the aerosol delivery system may be
accessible for refilling the device.
[0095] In this example, the smoking substitute system 100 is a closed system vaping system,
wherein the component 104 includes a sealed tank 106 and is intended for single-use
only. The component 104 is removably engageable with the device 102 (i.e. for removal
and replacement). Fig. 1A shows the smoking substitute system 100 with the device
102 physically coupled to the component 104, Fig. 1B shows the device 102 of the smoking
substitute system 100 without the component 104, and Fig. 1C shows the component 104
of the smoking substitute system 100 without the device 102.
[0096] The device 102 and the component 104 are configured to be physically coupled together
by pushing the component 104 into a cavity at an upper end 108 of the device 102,
such that there is an interference fit between the device 102 and the component 104.
In other examples, the device 102 and the component may be coupled by screwing one
onto the other, or through a bayonet fitting.
[0097] The component 104 includes a mouthpiece at an upper end 109 of the component 104,
and one or more air inlets (not shown) in fluid communication with the mouthpiece
such that air can be drawn into and through the component 104 along an inhalation
pathway when a user inhales through the mouthpiece. The tank 106 containing e-liquid
is located at the lower end 111 of the component 104.
[0098] The lower end 110 of the device 102 also includes a light 116 (e.g. an LED) located
behind a small translucent cover. The light 116 may be configured to illuminate when
the smoking substitute system 100 is activated and/or when charging. Whilst not shown,
the component 104 may identify itself to the device 102, via an electrical interface,
RFID chip, or barcode.
[0099] The lower end 110 of the device 102 also includes a charging connection 115, which
is usable to charge a battery within the device 102. The charging connection 115 can
also be used to transfer data to and from the device, for example to update firmware
thereon.
[0100] Figs. 2A and 2B are schematic drawings of the device 102 and component 104. As is
apparent from Fig. 2A, the device 102 includes a power source 118, a controller 120,
a memory 122, a wireless interface 124, an electrical interface 126, and, optionally,
one or more additional components 128.
[0101] The power source 118 is preferably a battery, more preferably a rechargeable battery.
The controller 120 may include a microprocessor, for example. The memory 122 preferably
includes non-volatile memory. The memory may include instructions which, when implemented,
cause the controller 120 to perform certain tasks or steps of a method.
[0102] The wireless interface 124 is preferably configured to communicate wirelessly with
another device, for example a mobile device, e.g. via Bluetooth
®. To this end, the wireless interface 124 could include a Bluetooth
® antenna. Other wireless communication interfaces, e.g. WiFi
®, are also possible. The wireless interface 124 may also be configured to communicate
wirelessly with a remote server.
[0103] The electrical interface 126 of the device 102 may include one or more electrical
contacts. The electrical interface 126 may be located in a base of the aperture in
the upper end 108 of the device 102. When the device 102 is physically coupled to
the component 104, the electrical interface 126 is configured to transfer electrical
power from the power source 118 to the component 104 (i.e. upon activation of the
smoking substitute system 100).
[0104] The electrical interface 126 may also be used to identify the component 104 from
a list of known components. For example, the component 104 may be a particular flavour
and/or have a certain concentration of nicotine (which may be identified by the electrical
interface 126). This can be indicated to the controller 120 of the device 102 when
the component 104 is connected to the device 102. Additionally, or alternatively,
there may be a separate communication interface provided in the device 102 and a corresponding
communication interface in the component 104 such that, when connected, the component
104 can identify itself to the device 102.
[0105] The additional components 128 of the device 102 may comprise the light 116 discussed
above.
[0106] The additional components 128 of the device 102 also comprises the charging connection
115 configured to receive power from the charging station (i.e. when the power source
118 is a rechargeable battery). This may be located at the lower end 110 of the device
102.
[0107] The additional components 128 of the device 102 may, if the power source 118 is a
rechargeable battery, include a battery charging control circuit, for controlling
the charging of the rechargeable battery. However, a battery charging control circuit
could equally be located in a charging station (if present).
[0108] The additional components 128 of the device 102 may include an inhalation airflow
sensor for detecting airflow in inhalation pathway through the smoking substitute
system 100, e.g. caused by a user inhaling through a mouthpiece portion 136 of the
component 104. The smoking substitute system 100 may be configured to be activated
when airflow is detected by the inhalation airflow sensor. This inhalation airflow
sensor could alternatively be included in the component 104. The inhalation airflow
sensor can be used to determine, for example, how heavily a user draws on the mouthpiece
or how many times a user draws on the mouthpiece in a particular time period.
[0109] The additional components 128 of the device 102 may include a user input, e.g. a
button. The smoking substitute system 100 may be configured to be activated when a
user interacts with the user input (e.g. presses the button). This provides an alternative
to the inhalation airflow sensor as a mechanism for activating the smoking substitute
system 100.
[0110] The additional components 128 of the system may additionally include the filter and
one or more exhalation airflow sensors as discussed below in relation to Figure 4
[0111] As shown in Fig. 2B, the component 104 includes the tank 106, an electrical interface
130, a vaporiser 132, one or more air inlets 134, a mouthpiece 136, and one or more
additional components 138.
[0112] The electrical interface 130 of the component 104 may include one or more electrical
contacts. The electrical interface 126 of the device 102 and an electrical interface
130 of the component 104 are configured to contact each other and thereby electrically
couple the device 102 to the component 104 when the lower end 111 of the component
104 is inserted into the upper end 108 of the device 102 (as shown in Fig. 1A). In
this way, electrical energy (e.g. in the form of an electrical current) is able to
be supplied from the power source 118 in the device 102 to the vaporiser 132 in the
component 104.
[0113] The vaporiser 132 is configured to heat and vaporise e-liquid contained in the tank
106 using electrical energy supplied from the power source 118. As will be described
further below, the vaporiser 132 includes a heating filament/heater track and a wick.
The wick draws e-liquid from the tank 106 and the heating filament heats/heater track
the e-liquid to vaporise the e-liquid.
[0114] The one or more air inlets 134 are preferably configured to allow air to be drawn
into the smoking substitute system 100, when a user inhales through the mouthpiece
136. When the component 104 is physically coupled to the device 102, the air inlets
134 receive air, which flows to the air inlets 134 along a gap between the device
102 and the lower end 111 of the component 104.
[0115] In operation, a user activates the smoking substitute system 100, e.g. through interaction
with a user input forming part of the device 102 or by inhaling through the mouthpiece
136 as described above. Upon activation, the controller 120 may supply electrical
energy from the power source 118 to the vaporiser 132 (via electrical interfaces 126,
130), which may cause the vaporiser 132 to heat e-liquid drawn from the tank 106 to
produce a vapour which is inhaled by a user through the mouthpiece 136.
[0116] An example of one of the one or more additional components 138 of the component 104
is an interface for obtaining an identifier of the component 104. As discussed above,
this interface may be, for example, an RFID reader, a barcode, a QR code reader, or
an electronic interface which is able to identify the component. The component 104
may, therefore 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 electronic interface
in the device 102.
[0117] The additional components 138 of the component may further include the filter and
one or more exhalation airflow sensors as discussed below in relation to Figure 3.
[0118] It should be appreciated that the smoking substitute system 100 shown in figures
1A to 2B is just one exemplary implementation of a smoking substitute system. For
example, the system could otherwise be in the form of an entirely disposable (single-use)
system or an open system in which the tank is refillable (rather than replaceable).
[0119] Fig. 3 is a schematic view of an example of the component 104 described above. The
component 104 comprises a tank 106 for storing e-liquid, a mouthpiece portion 136
and a conduit 140 extending along a longitudinal axis of the component 104. In the
illustrated embodiment the conduit 140 is in the form of a tube having a substantially
circular transverse cross-section (i.e. transverse to the longitudinal axis). The
tank 106 surrounds the conduit 140, such that the conduit 140 extends centrally through
the tank 106.
[0120] A component housing 142 defines an outer casing of the component 104. The component
housing 142 extends from a lower shell 158 at the lower end 111 of the component 104
to the mouthpiece portion 136 at the upper end 109 of the component 104. The component
housing may define a lip or shoulder which acts as a stop feature when the component
104 is inserted into the device 102 (i.e. by contact with an upper edge of the device
102).
[0121] The tank 106, the conduit 140 and the mouthpiece portion 136 are integrally formed
with each other so as to form a single unitary component and may e.g. be formed by
way of an injection moulding process. Such a component may be formed of a thermoplastic
material.
[0122] The mouthpiece portion 136 comprises a mouthpiece aperture 148 defining an outlet
of the conduit 140. The vaporiser 132 is downstream of the inlet 134 of the component
104 and is fluidly connected to the mouthpiece aperture 148 (i.e. outlet) by the conduit
140.
[0123] In some embodiments, the vaporiser 132 comprises a porous ceramic wick and a heater
track (not shown) printed onto the bottom surface (facing the inlet 34) of the ceramic
wick. The vaporiser 132 forms the base of the tank 106 so that the aerosol precursor
is in contact with the wick and liquid aerosol precursor can move axially into the
wick.
[0124] In other embodiments, the vaporiser 132 comprises a porous cylindrical wick with
a coiled heating filament, the wick extending into an annular portion of the tank
surrounding the vaporiser so that liquid aerosol precursor can move radially into
the wick.
[0125] The aerosol precursor is heated by the heater track or heating filament (when activated
e.g. by detection of inhalation), which causes the aerosol precursor to be vaporised
and to be entrained in air flowing past the wick. This vaporised liquid may cool to
form an aerosol in the conduit 140, which may then be inhaled by a user.
[0126] The lower shell 158 of the component housing 142 has an opening that accommodates
the electrical interface 119 of the consumable component 102 comprising two electrical
contacts 136a, 136b that are electrically connected to the heater track. In this way,
when the consumable component 104 is engaged with the device 102, power can be supplied
from the power source 118 of the device to the heater track/heating filament.
[0127] The component housing 142 defines a filter chamber 220 that is in fluid communication
with the mouthpiece aperture 148 via a bypass channel 221.
[0128] The component 104 further comprises a bypass valve, such as a one-way valve, (not
shown) for directing air into the bypass channel 221 so that exhaled air does not
pass the vaporiser 132.
[0129] The valve may be provided in or close to the mouthpiece aperture 148.
[0130] Figure 3 shows the filter chamber 220 in the mouthpiece portion 136 of the component
104 but it may be provided in any location within the component e.g. adjacent the
tank 106 or adjacent the vaporiser 132.
[0131] An exhalation port 223 extends from the filter chamber 220 to the exterior of the
system through the component housing 142.
[0132] Figure 4 shows an alternative embodiment in which the filter chamber 220' is provided
in the device 102 rather than in the component 104. In this embodiment, the bypass
channel 221 extends from proximal the mouthpiece aperture 148', through the component
104 (avoiding the vaporiser 132) and into the device.
[0133] When a user exhales, exhaled air is forced into the system via the mouthpiece aperture
148. Therefore, the user does not have to exhale (and therefore does not have to release
leftover/remnant vapour that may contain nicotine, contaminants and/or smells/flavours)
into their ambient environment.
[0134] The filter chamber 220, 220' contains a filter formed of filter material e.g. a porous
filter material which may be fibrous material, a meshed material or may be porous
network. For example the porous filter material may comprise cellulose acetate tow.
[0135] The filter is removably located within the filter chamber 220 and can be replaced.
For example, the filter chamber 220' may comprise an opening which is in communication
with the cavity for receiving the consumable component 104 so that the filter can
be replaced by removing the component 104 from the device 102 to reveal the opening.
[0136] In general terms, the filter material is configured to purify the exhaled air and
in particular to remove remnants of the vapour that was previously generated by the
vaporiser 132.
[0137] As a result, when the exhaled air exits component 104 or device 102 via the exhalation
outlet 222, 222', it will comprise substantially clean, purified air, and will comprise
little or no remnant of the vapour that the vaporiser 132 previously generated.
[0138] At least one exhalation airflow sensor (not specifically shown) is provided in the
system - it may be provided in the component 104 or in the device. The at least one
exhalation sensor is configured to detect an airflow rate of exhaled air passing through
the filter within the filter chamber 220, 220'. The sensor may therefore be referred
to as an "airflow sensor". It may be a pressure sensor.
[0139] The at least one exhalation airflow sensor is provided in, or in communication with
the bypass channel 221, 221' and/or filter chamber 220, 220' and/or the exhalation
port 223, 223' which leads from the filter chamber 220, 220' to the exhalation outlet
222, 222'.
[0140] The system may comprise a first exhalation airflow sensor upstream of the filter
chamber 220, 220' and a second exhalation sensor downstream of the filter chamber
220, 220', for comparison purposes i.e. to detect an airflow rate/pressure/volume
drop across the filter/filter chamber 220, 220'.
[0141] The exhalation airflow sensor(s) is/are in communication with a controller 12 in
the device 102. The controller is configured to use the data regarding the detected
drop in airflow rate/pressure volume of exhaled air through the filter in the filter
chamber 220, 220' to determine a saturation state of the filter.
[0142] In general terms, when the filter becomes (or approaches becoming) saturated, the
airflow rate of an exhaled airstream passing through the filter will reduce, because
it has become more difficult for the airstream to pass through the filter.
[0143] The controller 12 may be configured to compare a detected drop in airflow rate/pressure/volume
of exhaled air passing through the filter within the filter chamber 220, 220' to a
predetermined thresholds. The controller 12 is configured to provide an output indicating
saturation of the filter when the detected drop in airflow rate/pressure/volume exceeds
a predetermined threshold.
[0144] The output may provide an indication to the user via feedback means, for example
comprising the LED 116 on the device when the filter is at or approaching saturation.
[0145] While exemplary embodiments have been described above, many equivalent modifications
and variations will be apparent to those skilled in the art when given this disclosure.
Accordingly, the exemplary embodiments set forth above are considered to be illustrative
and not limiting.
[0146] 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.
[0147] 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%.
[0148] 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.