Switched reluctance motor
11716002 · 2023-08-01
Assignee
Inventors
- Aleksandr S. Nagorny (Canoga Park, CA, US)
- Siavash Sadeghi (Northridge, CA, US)
- David James Fleming (Cardiff, CA, US)
- Michael Bruce Moir (Newbury, CA, US)
Cpc classification
H02K5/04
ELECTRICITY
H02K19/103
ELECTRICITY
International classification
H02K1/24
ELECTRICITY
A61M16/00
HUMAN NECESSITIES
A61M16/08
HUMAN NECESSITIES
H02K5/04
ELECTRICITY
Abstract
A stator assembly has coils in a distributed winding configuration. A poly-phase switched reluctance motor assembly may include a stator assembly with multiple coils in a distributed winding configuration. The stator assembly may have a central bore into which a rotor assembly having multiple poles is received and configured to rotate. A method of controlling a switched reluctance motor may include at least three phases wherein during each conduction period a first phase is energized with negative direction current, a second phase is energized with positive current and there is at least one non-energized phase. During each commutation period either the first phase or second phase switches off to a non-energized state and one of the non-energized phases switches on to an energized state with the same direction current as the first or second phase that was switched off. The switched reluctance motor may include a distributed winding configuration.
Claims
1. A poly-phase switched reluctance motor assembly comprising: a stator assembly including a plurality of coils and a stator with a central bore; and a rotor assembly having a plurality of rotor poles, the rotor assembly being arranged within the central bore of the stator assembly and configured to rotate therein, wherein the plurality of coils are configured in a distributed winding configuration, wherein the stator includes a plurality of projecting stator teeth forming a plurality of stator slots therebetween, wherein the stator assembly defines a stator central angle and the rotor assembly defines a rotor central angle, the stator central angle and the rotor central angle having a difference in a range of 5 degrees to 30 degrees, and wherein the stator assembly is configured to operate with at least three phases that have direct current applied, at least in part, as a positive direction current and a negative direction current.
2. The poly-phase switched reluctance motor assembly of claim 1, wherein each of the plurality of stator slots comprises a coil segment of one of the plurality of coils.
3. The poly-phase switched reluctance motor assembly of claim 1, wherein the plurality of coils includes a coil group for each phase of the poly-phase switched reluctance motor and each of the coils in each coil group includes a pair of coil segments, the coil segments for each coil group being uniformly distributed between the stator slots.
4. The poly-phase switched reluctance motor assembly of claim 3, wherein each coil group comprises at least one coil.
5. The poly-phase switched reluctance motor assembly of claim 1, wherein the stator has an outer diameter less than 50 mm.
6. The poly-phase switched reluctance motor assembly of claim 5, wherein the stator has an outer diameter less than or equal to 45 mm.
7. The poly-phase switched reluctance motor assembly of claim 1, wherein a width of each rotor pole is wider than a width of one of the plurality of stator teeth.
8. The poly-phase switched reluctance motor assembly of claim 1, wherein each rotor pole width is equal.
9. The poly-phase switched reluctance motor assembly of claim 1, wherein each stator tooth width is equal.
10. The poly-phase switched reluctance motor assembly of claim 1, wherein the difference between the stator central angle and the rotor central angle is about 27 degrees.
11. The poly-phase switched reluctance motor assembly of claim 1, wherein each of the stator teeth comprises teeth tips.
12. A positive airway pressure device comprising a poly-phase switched reluctance motor assembly according to claim 1, wherein the positive airway pressure device is configured to provide a supply of pressurized breathable gas.
13. A system for treating a respiratory disorder comprising: a therapy device comprising a poly-phase switched reluctance motor assembly according to claim 1, the therapy device being configured to provide a supply of pressurized breathable gas; an air delivery conduit; and a patient interface configured to receive the supply of pressurized gas from the therapy device via the air delivery conduit and to deliver the supply of pressurized gas to a patient.
14. The system of claim 13, further comprising a humidifier configured to humidify the supply of pressurized gas.
15. A stator assembly for a poly-phase switched reluctance motor comprising: a plurality of stator teeth separated by stator slots and surrounding a central bore; and a plurality of coils that are configured in a distributed winding configuration, the plurality of coils include a coil group for each phase of the poly-phased switched reluctance motor, wherein the central bore is configured to receive a rotor assembly having a plurality of rotor poles and a number of stator slots, wherein the stator assembly defines a stator central angle and the rotor assembly defines a rotor central angle, the stator central angle and the rotor central angle having a difference in a range of 5 degrees to 30 degrees, and wherein the stator assembly is configured to operate with at least three phases that have direct current applied, at least in part, as a positive direction current and a negative direction current.
16. The stator assembly of claim 15, wherein each of the stator slots comprises a coil segment of one of the coils of the plurality of coils.
17. The stator assembly of claim 16, wherein each of the coil segments of a coil group are uniformly distributed between the stator slots.
18. The stator assembly of claim 15, wherein each coil group comprises at least one coil.
19. The stator assembly of claim 15, wherein a width of each of the stator teeth of the plurality of stator teeth is less than a width of a rotor pole.
20. The stator assembly of claim 15, wherein the rotor poles of the received rotor assembly have widths that are equal.
21. The stator assembly of claim 15, wherein each stator tooth width is equal.
22. The stator assembly of claim 15, wherein the stator has an outer diameter less than 50 mm.
23. The stator assembly of claim 22, wherein the stator has an outer diameter less than or equal to 45 mm.
24. The stator assembly of claim 15, wherein the difference between the stator central angle and the rotor central angle is about 27 degrees.
25. The stator assembly of claim 15, wherein each of the stator teeth comprises teeth tips.
26. The stator assembly of claim 15, wherein the stator assembly is a component of the poly-phase switched reluctance motor in a blower.
27. The stator assembly of claim 15, wherein the stator assembly is a component of the poly-phase switched reluctance motor in a flow generator of a respiratory therapy device.
28. A method of controlling a switched reluctance motor, the switched reluctance motor comprising at least three phases, the method comprising: during each conduction period energizing a first phase with a first current, energizing a second phase with a second current and having at least one non-energized phase; and during each commutation period switching off one of the first phase or the second phase to a non-energized state and switching on one of the non-energized phases to an energized state with a same direction current as the first or second phase that was switched off, wherein the switched reluctance motor has a stator assembly defining a stator central angle and a rotor assembly defining a rotor central angle, the stator central angle and the rotor central angle having a difference in a range of 5 to 30 degrees.
29. The method of claim 28, wherein the switched reluctance motor includes a distributed winding configuration.
30. The method of claim 28, wherein the difference between the stator central angle and the rotor central angle is about 27 degrees.
31. The method of claim 28, wherein the switched reluctance motor has a plurality of stator teeth, each comprising teeth tips.
32. The method of claim 28, wherein the switched reluctance motor is a component of a therapy device configured to supply pressurized gas.
Description
7 BRIEF DESCRIPTION OF THE SEVERAL VIEWS OF THE DRAWINGS
(1) The present technology is illustrated by way of example, and not by way of limitation, in the figures of the accompanying drawings, in which like reference numerals refer to similar elements including:
7.1 Motor
(2)
(3)
(4)
(5)
(6)
(7)
(8)
(9)
(10)
(11)
(12)
(13)
(14)
(15)
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(19)
(20)
7.2 Motor Assembly
(21)
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7.3 System
(29)
7.4 PAP Device
(30)
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7.5 Humidifier
(35)
(36)
8 DETAILED DESCRIPTION OF EXAMPLES OF THE TECHNOLOGY
(37) Before the present technology is described in further detail, it is to be understood that the technology is not limited to the particular examples described herein, which may vary. It is also to be understood that the terminology used in this disclosure is for the purpose of describing only the particular examples discussed herein, and is not intended to be limiting.
8.1 Switched Reluctance Motor
8.1.1 Stator
(38) In one form, the present technology comprises a switched reluctance motor including a stator having distributed coil windings. In a case of a distributed windings configuration, the coils are placed or wound into the slots. With such a distributed winding, each coil winding may encircle or encompass at least two stator teeth (or more) while skipping over at least one stator slot (or more). The coils may have full pitch or fractional pitch. The number of slots that are occupied with the coils of one phase depend on the number of rotor poles and a winding distribution parameter. The winding distribution parameter indicates how many adjacent slots are occupied with coil segments of the same phase.
(39) In the exemplary stator assemblies as shown in
(40)
(41)
(42) Although
Total number of stator slots=number of phases×number of rotor poles×winding distribution parameter.
Thus, the total number of stator slots may be a multiple of number of phases and number of rotor poles of the motor. Moreover, the total number of stator slots may be a multiple of a winding distribution parameter.
(43) The stator is formed as a lamination stack for example of steel laminations such as silicon steel e.g. M19 grade silicon steel (M19_29G). The rotor may be formed of the same material as the stator or another type of ferromagnetic material like ferrite or iron cobalt alloys. The coils may be formed of any wire gauge preferably in the range of 26 to 32 gauge wire, for example, each of the coils may be formed from American wire gauge (AWG) 30. The number of turns of the wire is determined by the voltage of the motor. For example the coils may include 30-40 turns per coils such as 34 turns per coil. In some cases, each turn of the coil may have one or more wires in hand such as a number in a range of 2 to 10 wires in hand per turn. For example, it may have six wires in hand per turn. Thus, in one example winding, the wire may be AWG 30, and each coil may have 34 turns with 6 wires in hand. However, a skilled addressee would understand that the coils may be formed of other material and include a different number of turns per coil and number of wires etc.
(44) A SR motor having a distributed winding configuration distributes the flux between the teeth that each of the phase coils is associated rather than concentrating the flux in a single stator tooth. This results in the radial electromagnetic forces acting between the stator and the rotor being distributed along the stator teeth that are associated with the energized coils. Thus, in the three phase stator arrangement illustrated in
(45) The SR motor including a distributed winding configuration of the present technology may have a low aligned to unaligned inductance ratio, such as an inductance ratio of less than 3, or less than 2.5 e.g. between 2 and 2.5.
(46) Advantageously the SR motor including a distributed winding configuration according to the present technology allows for smaller lower power SR motors to be made that produce enough torque to run small high speed devices (up to 60,000 rpm). A small SR motor is understood to mean a SR motor having a stator outer diameter of less than 50 mm, such as 48 mm, 47 mm, 46 mm, 45 mm, 44 mm, 43 mm or less. However, it is to be understood that a SR motor having a distributed winding configuration may also be used in larger motors than have stator outer diameters greater than 50 mm.
8.1.2 Rotor
(47) The rotor includes at least two rotor poles 130, 230, the rotor poles form rotor teeth that extend out from a central rotor core. In
(48) In some versions of the present technology, each stator tooth may have tooth tips 213a, 213b (labeled in
(49) The central angles of the stator and rotor poles may be as significant as absolute width values of the teeth. For example, in some typical motor designs, the central angle of the stator and rotor poles may be approximately the same or have a very small difference between them such as a few degrees. However, in some versions of the present technology, the angles may be significantly different, such as having an angle difference of more than several degrees (e.g., more than 5 degrees such as in a difference range from 3 degrees to 40 degrees, or such as in a difference range of 5 degrees to 30 degrees. For example, the stator central angle, such as the angle formed from the center of the stator with imaginary lines extending radially to the edges of a stator's tooth or stator's tips (see, e.g., angle SA illustrated in
(50) The rotor may be formed of a suitable material such as silicon steel e.g. M19 grade silicon steel (M19_29G) or another type of ferromagnetic material like ferrite or iron cobalt alloys.
8.1.3 Motor Control
(51) As mentioned previously, torque in SR motors is proportional to the difference in a phase self-inductances in an aligned and non-aligned position when the appropriate phase is energized. It has been determined that using a distributed stator winding configuration in a SR motor of the present technology may produce a significant mutual inductance variation between certain positions of the rotor. This mutual inductance may be utilized to produce a higher torque at small power (less than hundred watts such as 90 Watts, 60 Watts or 50 Watts) SR motor design.
(52) The stator of the SR motor of the present technology includes at least three motor phases. Due to the mutual inductance producing a large portion of the torque, the SR motor of the present technology may be configured to energize two phases at the same time during each conduction period. A first phase may be energized with a positive direction current and a second phase may be energized with a negative direction current resulting in a net flux increase in the motor and producing a higher torque. Two phases are energised at the same time and follow a specific sequence to cause the rotor to rotate. Each phase of the motor may be energized with the same current value during at least two consecutive conduction periods. For example in some configurations one of the two energized phases is switched off to a non-energized state and one of the non-energized phases is switched on to an energized state during each commutation period. The timing of the commutation period or switching is controlled to facilitate smooth rotation of the motor and reduce cogging.
(53)
(54)
(55)
Where Ta the instantaneous torque value, i.sub.a, i.sub.b and i.sub.c are instantaneous values of the current in phases A, B and C respectively. L.sub.aa is the total inductance of phase A. L.sub.ab is the mutual inductance between phases A and B and L.sub.ac is the mutual inductance between phases A and C respectively.
(56) In contrast in a conventional SR motor, where only the self-inductance component is producing the torque, i.e.
(57)
(58) A method of controlling a switched reluctance motor comprising at least three phases may include during each conduction period energizing a first phase with a negative direction current, energizing a second phase with a positive current and having at least one non-energized phase and during each commutation period switching off one of the first phase or the second phase to a non-energized state and switching on one of the non-energized phases to an energized state with the same direction current as the first or second phase that was switched off. The switched reluctance motor may include a distributed winding configuration as described above.
(59) In some aspects of the present technology the SR motor may be controlled using a sensorless control. In this arrangement when the rotor passes the non-energized phase, the back EMF, induced in the phase can be detected and filtered in order to remove the noise. The signal is proportional to the rotor angle and may be used to estimate the position of the rotor.
8.1.4 Motor Assembly
(60) An example of a motor assembly 3002 that may be implemented with the switched reluctance motor technology described herein is illustrated in
(61) As seen in more detail in the cross sectional view of
(62) The rotor assembly 3150 may include a rotor in any configuration as previously described such as the rotor configuration also illustrated in
8.2 Treatment Systems
(63) In one form, the present technology comprises apparatus for treating a respiratory disorder. The apparatus may comprise a flow generator or blower including a switched reluctance motor for supplying pressurised respiratory gas, such as air, to the patient 1000 via an air delivery tube 4170 leading to a patient interface 3000.
8.3 Therapy
(64) In one form, the present technology comprises method for treating a respiratory disorder comprising the step of applying positive pressure to the entrance of the airways of a patient 1000 using a pressure device including a switched reluctance motor.
8.3.1 Nasal CPAP for OSA
(65) In one form, the present technology comprises a method of treating Obstructive Sleep Apnea in a patient by applying nasal continuous positive airway pressure to the patient using a patient interface.
(66) In certain embodiments of the present technology, a supply of air at positive pressure is provided to the nasal passages of the patient via one or both nares.
(67) A patient interface 3000 is provided as seen in
8.4 PAP Device 4000
(68) As shown in
(69) The pneumatic path of the PAP device 4000 preferably comprises an inlet air filter 4112, an inlet muffler 4122, a controllable pressure device 4140 capable of supplying air at positive pressure (preferably a blower 4142) including a motor 4144, and an outlet muffler 4124. One or more transducers 4270 such as pressure sensors 4274, flow sensors 4272 and speed sensors 4276 are included in the pneumatic path.
(70) The preferred pneumatic block 4020 comprises a portion of the pneumatic path that is located within the external housing 4010.
(71) The PAP device 4000 may include an electrical power supply 4210, one or more input devices 4220, a central controller 4230, a therapy device controller 4240, a therapy device 4245, one or more protection circuits 4250, memory 4260, transducers 4270, data communication interface 4280 and one or more output devices 4290. Electrical components 4200 may be mounted on a single Printed Circuit Board Assembly (PCBA) 4202. In an alternative form, the PAP device 4000 may include more than one PCBA 4202.
(72) The central controller 4230 of the PAP device 4000 is programmed to execute one or more algorithm modules 4300, preferably including a pre-processing module 4310, a therapy engine module 4320, a therapy control module 4330, and further preferably a fault condition module 4340.
8.4.1 PAP Device Mechanical & Pneumatic Components 4100
8.4.1.1 Air Filter(s) 4110
(73) A PAP device in accordance with one form of the present technology may include an air filter 4110, or a plurality of air filters 4110.
(74) In one form, an inlet air filter 4112 is located at the beginning of the pneumatic path upstream of a blower 4142. See
(75) In one form, an outlet air filter 4114, for example an antibacterial filter, is located between an outlet of the pneumatic block 4020 and a patient interface 3000. See
8.4.1.2 Muffler(s) 4120
(76) In one form of the present technology, an inlet muffler 4122 is located in the pneumatic path upstream of a blower 4142. See
(77) In one form of the present technology, an outlet muffler 4124 is located in the pneumatic path between the blower 4142 and a patient interface 3000. See
8.4.1.3 Pressure Device 4140
(78) In a preferred form of the present technology, a pressure device 4140 for producing a flow of air at positive pressure is a controllable blower 4142. For example the blower may include a switched reluctance motor 4144 with one or more impellers housed in a volute. The blower may be preferably capable of delivering a supply of air, for example about 120 litres/minute, at a positive pressure in a range from about 4 cmH.sub.2O to about 20 cmH.sub.2O, or in other forms up to about 30 cmH.sub.2O.
(79) The pressure device 4140 is under the control of the therapy device controller 4240.
8.4.1.4 Transducer(s) 4270
(80) In one form of the present technology, one or more transducers 4270 are located upstream of the pressure device 4140. The one or more transducers 4270 are constructed and arranged to measure properties of the air at that point in the pneumatic path.
(81) In one form of the present technology, one or more transducers 4270 are located downstream of the pressure device 4140, and upstream of the air circuit 4170. The one or more transducers 4270 are constructed and arranged to measure properties of the air at that point in the pneumatic path.
(82) In one form of the present technology, one or more transducers 4270 are located proximate to the patient interface 3000.
8.4.1.5 Anti-Spill Back Valve 4160
(83) In one form of the present technology, an anti-spill back valve is located between the humidifier 5000 and the pneumatic block 4020. The anti-spill back valve is constructed and arranged to reduce the risk that water will flow upstream from the humidifier 5000, for example to the motor 4144.
8.4.1.6 Air Circuit 4170
(84) An air circuit 4170 in accordance with an aspect of the present technology is constructed and arranged to allow a flow of air or breathable gasses between the pneumatic block 4020 and the patient interface 3000.
8.4.1.7 Oxygen Delivery 4180
(85) In one form of the present technology, supplemental oxygen 4180 is delivered to a point in the pneumatic path.
(86) In one form of the present technology, supplemental oxygen 4180 is delivered upstream of the pneumatic block 4020.
(87) In one form of the present technology, supplemental oxygen 4180 is delivered to the air circuit 4170.
(88) In one form of the present technology, supplemental oxygen 4180 is delivered to the patient interface 3000.
8.4.2 PAP Device Electrical Components 4200
8.4.2.1 Power Supply 4210
(89) Power supply 4210 supplies power to the other components of the basic PAP device 4000: the input device 4220, the central controller 4230, the therapy device 4245, and the output device 4290.
(90) In one form of the present technology, power supply 4210 is internal of the external housing 4010 of the PAP device 4000. In another form of the present technology, power supply 4210 is external of the external housing 4010 of the PAP device 4000.
(91) In one form of the present technology power supply 4210 provides electrical power to the PAP device 4000 only. In another form of the present technology, power supply 4210 provides electrical power to both PAP device 4000 and humidifier 5000.
8.4.2.2 Input Device(s) 4220
(92) A PAP device 4000 may include one or more input devices 4220. Input devices 4220 comprises buttons, switches or dials to allow a person to interact with the PAP device 4000. The buttons, switches or dials may be physical devices, or software devices accessible via a touch screen. The buttons, switches or dials may, in one form, be physically connected to the external housing 4010, or may, in another form, be in wireless communication with a receiver that is in electrical connection to the central controller 4230.
(93) In one form the input device 4220 may be constructed and arranged to allow a person to select a value and/or a menu option.
8.4.2.3 Central Controller or Processor 4230
(94) In one form of the present technology, the central controller or processor 4230 is a dedicated electronic circuit configured to receive input signal(s) from the input device 4220, and to provide output signal(s) to the output device 4290 and/or the therapy device controller 4240.
(95) In one form, the central controller 4230 is an application-specific integrated circuit. In another form, the central controller 4230 comprises discrete electronic components.
(96) In one form of the present technology, the central controller 4230 is a processor suitable to control a PAP device 4000 such as an x86 INTEL processor.
(97) A processor 4230 suitable to control a PAP device 4000 in accordance with another form of the present technology includes a processor based on ARM Cortex-M processor from ARM Holdings. For example, an STM32 series microcontroller from ST MICROELECTRONICS may be used.
(98) Another processor 4230 suitable to control a PAP device 4000 in accordance with a further alternative form of the present technology includes a member selected from the family ARM9-based 32-bit RISC CPUs. For example, an STR9 series microcontroller from ST MICROELECTRONICS may be used.
(99) In certain alternative forms of the present technology, a 16-bit RISC CPU may be used as the processor 4230 for the PAP device 4000. For example a processor from the MSP430 family of microcontrollers, manufactured by TEXAS INSTRUMENTS, may be used.
(100) The processor 4230 is configured to receive input signal(s) from one or more transducers 4270, and one or more input devices 4220.
(101) The processor 4230 is configured to provide output signal(s) to one or more of an output device 4290, a therapy device controller 4240, a data communication interface 4280 and humidifier controller 5250.
(102) In some forms of the present technology, the processor 4230, or multiple such processors, is configured to implement the one or more methodologies described herein such as the one or more algorithms 4300 expressed as computer programs stored in a non-transitory computer readable storage medium, such as memory 4260. In some cases, as previously discussed, such processor(s) may be integrated with a PAP device 4000. However, in some forms of the present technology the processor(s) may be implemented discretely from the flow generation components of the PAP device 4000, such as for purpose of performing any of the methodologies described herein without directly controlling delivery of a respiratory treatment. For example, such a processor may perform any of the methodologies described herein for purposes of determining control settings for a ventilator or other respiratory related events by analysis of stored data such as from any of the sensors described herein.
(103) Preferably PAP device 4000 includes a clock 4232 that is connected to the central controller 4230.
8.4.2.4 Therapy Device 4245
(104) In one form of the present technology, the therapy device 4245 is configured to deliver therapy to a patient 1000 under the control of the central controller 4230. Preferably the therapy device 4245 is a positive air pressure device 4140.
8.4.2.5 Therapy Device Controller 4240
(105) In one form of the present technology, therapy device controller 4240 is a therapy control module 4330 such as for pressure control that forms part of the algorithms 4300 executed by the processor 4230.
(106) In one form of the present technology, therapy device controller 4240 is a dedicated motor control integrated circuit. For example, in one form a MC33035 brushless DC motor controller, manufactured by ONSEMI is used.
8.4.2.6 Protection Circuits 4250
(107) Preferably a PAP device 4000 in accordance with the present technology comprises one or more protection circuits 4250.
(108) One form of protection circuit 4250 in accordance with the present technology is an electrical protection circuit.
(109) One form of protection circuit 4250 in accordance with the present technology is a temperature or pressure safety circuit.
8.4.2.7 Memory 4260
(110) In accordance with one form of the present technology the PAP device 4000 includes memory 4260, preferably non-volatile memory. In some forms, memory 4260 may include battery powered static RAM. In some forms, memory 4260 may include volatile RAM.
(111) Preferably memory 4260 is located on PCBA 4202. Memory 4260 may be in the form of EEPROM, or NAND flash.
(112) Additionally or alternatively, PAP device 4000 includes removable form of memory 4260, for example a memory card made in accordance with the Secure Digital (SD) standard.
(113) In one form of the present technology, the memory 4260 acts as a non-transitory computer readable storage medium on which is stored computer program instructions expressing the one or more methodologies described herein, such as the one or more algorithms 4300.
8.4.2.8 Transducers 4270
(114) Transducers may be internal of the device, or external of the PAP device. External transducers may be located for example on or form part of the air delivery circuit, e.g. the patient interface. External transducers may be in the form of non-contact sensors such as a Doppler radar movement sensor that transmit or transfer data to the PAP device.
8.4.2.8.1 Flow
(115) A flow transducer 4272 in accordance with the present technology may be based on a differential pressure transducer, for example, an SDP600 Series differential pressure transducer from SENSIRION. The differential pressure transducer is in fluid communication with the pneumatic circuit, with one of each of the pressure transducers connected to respective first and second points in a flow restricting element. Other flow sensors may also be implemented such as a hot wire flow sensor.
(116) In use, a signal representing total flow Qt from the flow transducer 4272 is received by the processor 4230.
8.4.2.8.2 Pressure
(117) A pressure transducer 4274 in accordance with the present technology is located in fluid communication with the pneumatic circuit. An example of a suitable pressure transducer is a sensor from the HONEYWELL ASDX series. An alternative suitable pressure transducer is a sensor from the NPA Series from GENERAL ELECTRIC.
(118) In use, a signal from the pressure transducer 4274, is received by the processor 4230. In one form, the signal from the pressure transducer 4274 is filtered prior to being received by the processor 4230.
8.4.2.8.3 Motor Speed
(119) In one form of the present technology a motor speed signal 4276 is generated. A motor speed signal 4276 is preferably provided by therapy device controller 4240. Motor speed may, for example, be generated by a speed sensor, such as a Hall effect sensor.
8.4.2.9 Data Communication Systems
(120) In one preferred form of the present technology, a data communication interface 4280 is provided, and is connected to processor 4230. Data communication interface 4280 is preferably connectable to remote external communication network 4282. Data communication interface 4280 is preferably connectable to local external communication network 4284. Preferably remote external communication network 4282 is connectable to remote external device 4286. Preferably local external communication network 4284 is connectable to local external device 4288.
(121) In one form, data communication interface 4280 is part of processor 4230. In another form, data communication interface 4280 is an integrated circuit that is separate from processor 4230.
(122) In one form, remote external communication network 4282 is the Internet. The data communication interface 4280 may use wired communication (e.g. via Ethernet, or optical fibre) or a wireless protocol to connect to the Internet.
(123) In one form, local external communication network 4284 utilises one or more communication standards, such as Bluetooth, or a consumer infrared protocol.
(124) In one form, remote external device 4286 is one or more computers, for example a cluster of networked computers. In one form, remote external device 4286 may be virtual computers, rather than physical computers. In either case, such remote external device 4286 may be accessible to an appropriately authorised person such as a clinician.
(125) Preferably local external device 4288 is a personal computer, mobile phone, tablet or remote control.
8.4.2.10 Output Devices Including Optional Display, Alarms
(126) An output device 4290 in accordance with the present technology may take the form of one or more of a visual, audio, and haptic output. A visual output may be a Liquid Crystal Display (LCD) or Light Emitting Diode (LED) display. An audio output may be a speaker or audio tone emitter.
8.4.2.10.1 Display Driver 4292
(127) A display driver 4292 receives as an input the characters, symbols, or images intended for display on the display 4294, and converts them to commands that cause the display 4294 to display those characters, symbols, or images.
8.4.2.10.2 Display 4294
(128) A display 4294 is configured to visually display characters, symbols, or images in response to commands received from the display driver 4292. For example, the display 4294 may be an eight-segment display, in which case the display driver 4292 converts each character or symbol, such as the figure “0”, to eight logical signals indicating whether the eight respective segments are to be activated to display a particular character or symbol.
8.4.3 PAP Device Algorithms 4300
8.4.3.1 Pre-Processing Module 4310
(129) An pre-processing module 4310 in accordance with the present technology receives as an input, raw data from a transducer, for example a flow or pressure transducer, and preferably performs one or more process steps to calculate one or more output values that will be used as an input to another module, for example a therapy engine module 4320.
(130) In one form of the present technology, the output values include the interface or mask pressure Pm, the respiratory flow Qr, and the leak flow Ql.
(131) In various forms of the present technology, the pre-processing module 4310 comprises one or more of the following algorithms: pressure compensation algorithm 4312, vent flow calculation algorithm 4314, leak flow algorithm 4316 and respiratory flow algorithm 4318.
(132) A pressure compensation algorithm 4312 may receive as an input a signal indicative of the pressure in the pneumatic path proximal to an outlet of the pneumatic block. The pressure compensation algorithm 4312 estimates the pressure drop in the air circuit 4170 and provides as an output an estimated pressure, Pm, in the patient interface 3000.
(133) A vent flow calculation algorithm 4314 may receive as an input an estimated pressure, Pm, in the patient interface 3000 and estimates a vent flow of air, Qv, from a vent 3400 in a patient interface 3000.
(134) A leak flow algorithm 4316 may receive as an input a total flow, Qt, and a vent flow Qv, and provides as an output a leak flow Ql by calculating an average of Qt-Qv over a period sufficiently long to include several breathing cycles, e.g. about 10 seconds.
(135) A respiratory flow algorithm 4318 may receive as an input a total flow, Qt, a vent flow, Qv, and a leak flow, Ql, and estimates a respiratory flow of air, Qr, to the patient, by subtracting the vent flow Qv and the leak flow Ql from the total flow Qt.
8.4.3.2 Therapy Engine Module 4320
(136) In one form of the present technology, a therapy engine module 4320 may receive as inputs one or more of a pressure, Pm, in a patient interface 3000, and a respiratory flow of air to a patient, Qr, and provides as an output, one or more therapy parameters, such as a CPAP treatment pressure Pt, a level of pressure support, and a target ventilation.
(137) In various forms of the present technology, the therapy engine module 4320 comprises one or more of the following algorithms: phase determination 4321, waveform determination 4322, ventilation determination 4323, flow limitation determination 4324, Apnea/hypopnea determination 4325, Snore determination 4326, Patency determination 4327 and Therapy parameter determination 4328.
(138) A phase determination algorithm 4321 may receive as an input a signal indicative of respiratory flow, Qr, and provides as an output a phase of a breathing cycle of a patient 1000. The phase output may be a discrete variable with values of one of inhalation, mid-inspiratory pause, and exhalation. Alternatively the phase output is a continuous variable, for example varying from 0 to 1, or 0 to 2 Pi.
(139) In one form, the phase output is determined to have a discrete value of inhalation when a respiratory flow Qr has a positive value that exceeds a positive threshold. In one form, a phase is determined to have a discrete value of exhalation when a respiratory flow Qr has a negative value that is more negative than a negative threshold.
(140) A waveform determination algorithm 4322 may receive as an input a value indicative of current patient ventilation, Vent, and provides as an output a waveform of pressure vs. phase. A ventilation determination algorithm 4323 may receive as an input a respiratory flow Qr, and determines a measure indicative of patient ventilation, Vent. For example the ventilation determination algorithm 4323 may determine a current value of patient ventilation, Vent, as half the low-pass filtered absolute value of respiratory flow, Qr.
(141) A flow limitation determination algorithm 4324 may receive as an input a respiratory flow signal Qr and provides as an output a metric of the extent to which the inspiratory portion of the breath exhibits inspiratory flow limitation.
(142) An Apnea/hypopnea determination algorithm 4325 may receive as an input a respiratory flow signal Qr and provide as an output a flag that indicates that an apnea or an hypopnea has been detected.
(143) An apnea may be said to have been detected when a function of respiratory flow Qr falls below a flow threshold for a predetermined period of time. The function may determine a peak flow, a relatively short-term mean flow, or a flow intermediate of relatively short-term mean and peak flow, for example an RMS flow. The flow threshold may be a relatively long-term measure of flow.
(144) A hypopnea may be said to have been detected when a function of respiratory flow Qr falls below a second flow threshold for a predetermined period of time. The function may determine a peak flow, a relatively short-term mean flow, or a flow intermediate of relatively short-term mean and peak flow, for example an RMS flow. The second flow threshold may be a relatively long-term measure of flow. The second flow threshold is greater than the flow threshold used to detect apneas.
(145) A snore determination algorithm 4326 may receive as an input a respiratory flow signal Qr and provides as an output a metric of the extent to which snoring is present. Preferably the snore determination algorithm 4326 comprises the step of determining the intensity of the flow signal in the range of 30-300 Hz. Further preferably, snore determination algorithm 4326 comprises a step of filtering the respiratory flow signal Qr to reduce background noise, e.g. the sound of airflow in the system from the blower. The snore determination algorithm 4326 may comprise comparing the noise generated during inspiration to the noise generated during expiration to determine the occurrence of snore, where the noise generated during expiration is considered to relate to the intrinsic device noise.
(146) In one form an airway patency algorithm 4327 may receive as an input a respiratory flow signal Qr, and determines the power of the signal in the frequency range of about 0.75 Hz and about 3 Hz. The presence of a peak in this frequency range is taken to indicate an open airway. The absence of a peak is taken to be an indication of a closed airway.
(147) In one form, the frequency range within which the peak is sought is the frequency of a small forced oscillation in the treatment pressure Pt. In one implementation, the forced oscillation is of frequency 2 Hz with amplitude about 1 cmH.sub.2O.
(148) In another form, an airway patency algorithm 4327 may receive as an input a respiratory flow signal Qr, and determines the presence or absence of a cardiogenic signal. The absence of a cardiogenic signal is taken to be an indication of a closed airway.
(149) A therapy parameter determination algorithm 4328 determines a target treatment pressure Pt to be delivered by the PAP device 4000. The therapy parameter determination algorithm 4328 receives as an input one of more of the following: i. A measure of respiratory phase; ii. A waveform; iii. A measure of ventilation; iv. A measure of inspiratory flow limitation; v. A measure of the presence of apnea and/or hypopnea; vi. A measure of the presence of snore; and vii. A measure of the patency of the airway.
(150) The therapy parameter determination algorithm 4328 determines the treatment pressure Pt as a function of indices or measures of one or more of flow limitation, apnea, hypopnea, patency, and snore. In one implementation, these measures are determined on a single breath basis, rather than on an aggregation of several previous breaths.
(151)
(152) At step 4530, the processor 4230 compares the measure of flow limitation with a third threshold. If the measure of flow limitation exceeds the third threshold, indicating inspiratory flow is limited, the method 4500 proceeds to step 4550; otherwise, the method 4500 proceeds to step 4560.
(153) At step 4550, the processor 4230 increases the treatment pressure Pt by a predetermined pressure increment ΔP, provided the increased treatment pressure Pt would not exceed an upper limit Pmax. In one implementation, the predetermined pressure increment ΔP and upper limit Pmax are 1 cmH.sub.2O and 20 cmH.sub.2O respectively. The method 4500 then returns to step 4520.
(154) At step 4560, the processor 4230 decreases the treatment pressure Pt by a decrement, provided the decreased treatment pressure Pt would not fall below a lower limit Pmin, such as a Pmin of 4 cmH.sub.2O. The method 4500 then returns to step 4520. In one implementation, the decrement is proportional to the value of Pt-Pmin, so that the decrease in Pt to the lower limit Pmin in the absence of any detected events is exponential. Alternatively, the decrement in Pt could be predetermined, so the decrease in Pt to the lower limit Pmin in the absence of any detected events is linear.
8.4.3.3 Therapy Control Module 4330
(155) A therapy control module 4330 in accordance with one aspect of the present technology may receive as an input a target treatment pressure Pt, and controls a therapy device 4245 to deliver that pressure. The therapy control module 4330 may receive as an input an EPAP pressure and an IPAP pressure, and controls a therapy device 4245 to deliver those respective pressures.
8.4.3.4 Detection of Fault Conditions
(156) In one form of the present technology, a processor executes one or more methods for the detection of fault conditions serving as a fault condition module 4340. Preferably the fault conditions detected by the one or more methods includes at least one of the following: Power failure (no power, or insufficient power) Transducer fault detection Failure to detect the presence of a component Operating parameters outside recommended ranges (e.g. pressure, flow, temperature, PaO.sub.2) Failure of a test alarm to generate a detectable alarm signal.
(157) Upon detection of the fault condition, the corresponding algorithm signals the presence of the fault by one or more of the following: Initiation of an audible, visual &/or kinetic (e.g. vibrating) alarm Sending a message to an external device Logging of the incident
8.5 Humidifier 5000
8.5.1 Humidifier Overview
(158) As shown in
(159) One or more transducers or sensors 5270, such as a temperature sensor, a relative humidity sensor, an absolute humidity sensor, a flow sensor or other such sensors may be present at one or more locations along the air path to measure the temperature, relative humidity, absolute humidity or flow rate at different locations to assist in controlling the humidifier and an optional heated air delivery conduit 4172. For example the heater plate 5120 may comprise a temperature sensor to measure the temperature of the heating plate. The one or more transducers or sensors 5270 may also be located external to the air path to measure the ambient conditions such as ambient temperature, ambient relative humidity and/or ambient absolute humidity.
(160) A heated air delivery conduit 4172 may comprise a heating element 4173 within or around the heated air delivery conduit 4172. For example wires may be positioned between the film and supporting ribs of a heated tube. The heated air delivery conduit 4172 may also comprise one or more transducers or sensors 5270 as described above.
8.6 Glossary
(161) For the purposes of the present technology disclosure, in certain forms of the present technology, one or more of the following definitions may apply. In other forms of the present technology, alternative definitions may apply.
(162) Air: In certain forms of the present technology, air supplied to a patient may be atmospheric air, and in other forms of the present technology atmospheric air may be supplemented with oxygen.
(163) Continuous Positive Airway Pressure (CPAP): CPAP treatment will be taken to mean the application of a supply of air or breathable gas to the entrance to the airways at a pressure that is continuously positive with respect to atmosphere, and preferably approximately constant through a respiratory cycle of a patient. In some forms, the pressure at the entrance to the airways will vary by a few centimeters of water within a single respiratory cycle, for example being higher during inhalation and lower during exhalation. In some forms, the pressure at the entrance to the airways will be slightly higher during exhalation, and slightly lower during inhalation. In some forms, the pressure will vary between different respiratory cycles of the patient, for example being increased in response to detection of indications of partial upper airway obstruction, and decreased in the absence of indications of partial upper airway obstruction.
(164) Controller: A device, or portion of a device that adjusts an output based on an input. For example one form of controller has a variable that is under control—the control variable—that constitutes the input to the device. The output of the device is a function of the current value of the control variable, and a set point for the variable. A servo-ventilator may include a controller that has ventilation as an input, a target ventilation as the set point, and level of pressure support as an output. Other forms of input may be one or more of oxygen saturation (SaO.sub.2), partial pressure of carbon dioxide (PCO.sub.2), movement, a signal from a photoplethysmogram, and peak flow. The set point of the controller may be one or more of fixed, variable or learned. For example, the set point in a ventilator may be a long term average of the measured ventilation of a patient. Another ventilator may have a ventilation set point that changes with time. A pressure controller may be configured to control a blower or pump to deliver air at a particular pressure.
(165) Therapy: Therapy in the present context may be one or more of positive pressure therapy, oxygen therapy, carbon dioxide therapy, control of dead space, and the administration of a drug.
(166) Transducers: A device for converting one form of energy or signal into another. A transducer may be a sensor or detector for converting mechanical energy (such as movement) into an electrical signal. Examples of transducers include pressure sensors, flow sensors, carbon dioxide (CO.sub.2) sensors, oxygen (O.sub.2) sensors, effort sensors, movement sensors, noise sensors, a plethysmograph, and cameras.
(167) Volute: The casing of the centrifugal pump that receives the air being pumped by the impeller, slowing down the flow rate of air and increasing the pressure. The cross-section of the volute increases in area towards the discharge port.
(168) Apnea: Preferably, apnea will be said to have occurred when flow falls below a predetermined threshold for a duration, e.g. 10 seconds. An obstructive apnea will be said to have occurred when, despite patient effort, some obstruction of the airway does not allow air to flow. A central apnea will be said to have occurred when an apnea is detected that is due to a reduction in breathing effort, or the absence of breathing effort.
(169) Breathing rate: The rate of spontaneous respiration of a patient, usually measured in breaths per minute.
(170) Effort (breathing): Preferably breathing effort will be said to be the work done by a spontaneously breathing person attempting to breathe.
(171) Expiratory portion of a breathing cycle: The period from the start of expiratory flow to the start of inspiratory flow.
(172) Flow limitation: Preferably, flow limitation will be taken to be the state of affairs in a patient's respiration where an increase in effort by the patient does not give rise to a corresponding increase in flow. Where flow limitation occurs during an inspiratory portion of the breathing cycle it may be described as inspiratory flow limitation. Where flow limitation occurs during an expiratory portion of the breathing cycle it may be described as expiratory flow limitation.
(173) Hypopnea: Preferably, a hypopnea will be taken to be a reduction in flow, but not a cessation of flow. In one form, a hypopnea may be said to have occurred when there is a reduction in flow below a threshold for a duration. In one form in adults, the following either of the following may be regarded as being hypopneas: (i) a 30% reduction in patient breathing for at least 10 seconds plus an associated 4% desaturation; or (ii) a reduction in patient breathing (but less than 50%) for at least 10 seconds, with an associated desaturation of at least 3% or an arousal.
(174) Patency (airway): The degree of the airway being open, or the extent to which the airway is open. A patent airway is open. Airway patency may be quantified, for example with a value of one (1) being patent, and a value of zero (0), being closed.
(175) Positive End-Expiratory Pressure (PEEP): The pressure above atmosphere in the lungs that exists at the end of expiration.
(176) Peakflow (Qpeak): The maximum value of flow during the inspiratory portion of the respiratory flow waveform.
(177) Respiratory flow, airflow, patient airflow, respiratory airflow (Qr): These synonymous terms may be understood to refer to the PAP device's estimate of respiratory airflow, as opposed to “true respiratory flow” or “true respiratory airflow”, which is the actual respiratory flow experienced by the patient, usually expressed in litres per minute.
(178) Upper airway obstruction (UAO): includes both partial and total upper airway obstruction. This may be associated with a state of flow limitation, in which the level of flow increases only slightly or may even decrease as the pressure difference across the upper airway increases (Starling resistor behaviour).
(179) Ventilation (Vent): A measure of the total amount of gas being exchanged by the patient's respiratory system, including both inspiratory and expiratory flow, per unit time. When expressed as a volume per minute, this quantity is often referred to as “minute ventilation”. Minute ventilation is sometimes given simply as a volume, understood to be the volume per minute.
(180) Flow rate: The instantaneous volume (or mass) of air delivered per unit time. While flow rate and ventilation have the same dimensions of volume or mass per unit time, flow rate is measured over a much shorter period of time. Flow may be nominally positive for the inspiratory portion of a breathing cycle of a patient, and hence negative for the expiratory portion of the breathing cycle of a patient. In some cases, a reference to flow rate will be a reference to a scalar quantity, namely a quantity having magnitude only. In other cases, a reference to flow rate will be a reference to a vector quantity, namely a quantity having both magnitude and direction. Flow will be given the symbol Q. Total flow, Qt, is the flow of air leaving the PAP device. Vent flow, Qv, is the flow of air leaving a vent to allow washout of exhaled gases. Leak flow, Ql, is the flow rate of unintentional leak from a patient interface system. Respiratory flow, Qr, is the flow of air that is received into the patient's respiratory system.
(181) Leak: Preferably, the word leak will be taken to be a flow of air to the ambient. Leak may be intentional, for example to allow for the washout of exhaled CO.sub.2. Leak may be unintentional, for example, as the result of an incomplete seal between a mask and a patient's face.
(182) Pressure: Force per unit area. Pressure may be measured in a range of units, including cmH.sub.2O, g-f/cm.sup.2, hectopascal. 1cmH.sub.2O is equal to 1 g-f/cm.sup.2 and is approximately 0.98 hectopascal. In this specification, unless otherwise stated, pressure is given in units of cmH.sub.2O. For nasal CPAP treatment of OSA, a reference to treatment pressure is a reference to a pressure in the range of about 4-20 cmH.sub.2O, or about 4-30 cmH.sub.2O. The pressure in the patient interface is given the symbol Pm.
(183) Sound Power: The energy per unit time carried by a sound wave. The sound power is proportional to the square of sound pressure multiplied by the area of the wavefront. Sound power is usually given in decibels SWL, that is, decibels relative to a reference power, normally taken as 10.sup.−12 watt.
(184) Sound Pressure: The local deviation from ambient pressure at a given time instant as a result of a sound wave travelling through a medium. Sound power is usually given in decibels SPL, that is, decibels relative to a reference power, normally taken as 20×10.sup.−6 pascal (Pa), considered the threshold of human hearing.
8.7 Other Remarks
(185) A portion of the disclosure of this patent document contains material which is subject to copyright protection. The copyright owner has no objection to the facsimile reproduction by anyone of the patent document or the patent disclosure, as it appears in the Patent and Trademark Office patent file or records, but otherwise reserves all copyright rights whatsoever.
(186) Unless the context clearly dictates otherwise and where a range of values is provided, it is understood that each intervening value, to the tenth of the unit of the lower limit, between the upper and lower limit of that range, and any other stated or intervening value in that stated range is encompassed within the technology. The upper and lower limits of these intervening ranges, which may be independently included in the intervening ranges, are also encompassed within the technology, subject to any specifically excluded limit in the stated range. Where the stated range includes one or both of the limits, ranges excluding either or both of those included limits are also included in the technology.
(187) Furthermore, where a value or values are stated herein as being implemented as part of the technology, it is understood that such values may be approximated, unless otherwise stated, and such values may be utilized to any suitable significant digit to the extent that a practical technical implementation may permit or require it.
(188) Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this technology belongs. Although any methods and materials similar or equivalent to those described herein can also be used in the practice or testing of the present technology, a limited number of the exemplary methods and materials are described herein.
(189) When a particular material is identified as being preferably used to construct a component, obvious alternative materials with similar properties may be used as a substitute. Furthermore, unless specified to the contrary, any and all components herein described are understood to be capable of being manufactured and, as such, may be manufactured together or separately.
(190) It must be noted that as used herein and in the appended claims, the singular forms “a”, “an”, and “the” include their plural equivalents, unless the context clearly dictates otherwise.
(191) All publications mentioned herein are incorporated by reference to disclose and describe the methods and/or materials which are the subject of those publications. The publications discussed herein are provided solely for their disclosure prior to the filing date of the present application. Nothing herein is to be construed as an admission that the present technology is not entitled to antedate such publication by virtue of prior invention. Further, the dates of publication provided may be different from the actual publication dates, which may need to be independently confirmed.
(192) Moreover, in interpreting the disclosure, all terms should be interpreted in the broadest reasonable manner consistent with the context. In particular, the terms “comprises” and “comprising” should be interpreted as referring to elements, components, or steps in a non-exclusive manner, indicating that the referenced elements, components, or steps may be present, or utilized, or combined with other elements, components, or steps that are not expressly referenced.
(193) The subject headings used in the detailed description are included only for the ease of reference of the reader and should not be used to limit the subject matter found throughout the disclosure or the claims. The subject headings should not be used in construing the scope of the claims or the claim limitations.
(194) Although the technology herein has been described with reference to particular embodiments, it is to be understood that these embodiments are merely illustrative of the principles and applications of the technology. In some instances, the terminology and symbols may imply specific details that are not required to practice the technology. For example, although the terms “first” and “second” may be used, unless otherwise specified, they are not intended to indicate any order but may be utilised to distinguish between distinct elements. Furthermore, although process steps in the methodologies may be described or illustrated in an order, such an ordering is not required. Those skilled in the art will recognize that such ordering may be modified and/or aspects thereof may be conducted concurrently or even synchronously.
(195) Further example versions of the technology may be considered in the following descriptive paragraphs:
(196) Example 1. A poly-phase switched reluctance motor assembly comprising:
(197) a stator assembly including a plurality of coils and a stator with a central bore, and
(198) a rotor assembly having a plurality of poles, the rotor assembly being arranged within the central bore of the stator assembly and configured to rotate therein,
(199) wherein the plurality of coils are configured in a distributed winding configuration,
(200) wherein the stator includes a plurality of projecting stator teeth forming a plurality of stator slots therebetween, and
(201) wherein a total number of stator slots is a multiple of number of phases and number of rotor poles of the motor.
(202) Example 2. The poly-phase switched reluctance motor assembly of Example 1 wherein each of the plurality of stator slots comprises a coil segment from one of the plurality of coils.
(203) Example 3. The poly-phase switched reluctance motor assembly according to any one of Examples 1-2, wherein the total number of stator slots further comprises a multiple of a winding distribution parameter, such that the total number of stator slots satisfies an equation consisting of:
Total number of stator slots=number of phases×number of rotor poles×winding distribution parameter.
(204) Example 4. The poly-phase switched reluctance motor assembly according to any one of Examples 1-3, wherein the plurality of coils includes a coil group for each phase of the poly-phase switched reluctance motor and each of the coils in a coil group includes a pair of coil segments, the coil segments for each coil group are uniformly distributed between the stator slots.
(205) Example 5. The poly-phase switched reluctance motor assembly according to Example 4, wherein each coil group comprises at least one coil.
(206) Example 6. The poly-phase switched reluctance motor assembly according to any one of Examples 1-5, including at least three motor phases and wherein in use two motor phases are energized and at least one phase is non-energized during a conduction period.
(207) Example 7. The poly-phase switched reluctance motor assembly according to Example 6, wherein one of the two energized phases is switched off to a non-energized state and one of the non-energized phases is switched on to an energized state during each commutation period.
(208) Example 8. The poly-phase switched reluctance motor assembly according to any one of Examples 6 or 7, wherein one of the two energized phases is provided with a positive direction current and the other of the two energized phases is provided with a negative direction current.
(209) Example 9. The poly-phase switched reluctance motor assembly according to Example 8, wherein each phase of the motor is energized with a current value during at least two consecutive conduction periods.
(210) Example 10. The poly-phase switched reluctance motor assembly according to any one of Examples 1-9, having an inductance ratio of less than 3.
(211) Example 11. The poly-phase switched reluctance motor assembly according to Example 10, wherein the inductance ratio is between 2 and 2.5.
(212) Example 12. The poly-phase switched reluctance motor assembly according to any one of Examples 1-11, wherein the stator has an outer diameter less than 50 mm.
(213) Example 13. The poly-phase switched reluctance motor assembly according to Example 12, wherein the stator has an outer diameter less than or equal to 45 mm.
(214) Example 14. The poly-phase switched reluctance motor assembly according to any one of Examples 1-13, wherein width of each rotor pole is wider than width of one of the plurality of stator teeth.
(215) Example 15. The poly-phase switched reluctance motor assembly according to any one of Examples 1-14, wherein the distributed winding configuration comprises a plurality of phases with at least one phase of the plurality of phases comprising a plurality of coil winding groups.
(216) Example 16. The poly-phase switched reluctance motor assembly according to any one of Examples 1-15 wherein each rotor pole width is equal.
(217) Example 17. The poly-phase switched reluctance motor assembly according to any one of Examples 1-16 wherein each stator slot width is equal.
(218) Example 18. The poly-phase switched reluctance motor assembly of any one of Examples 1-17 wherein the stator assembly and rotor assembly are configured to have a difference between a stator central angle and a rotor central angle in a difference range of 5 to 30 degrees.
(219) Example 19. The poly-phase switched reluctance motor assembly of Example 18 wherein the difference between a stator central angle and a rotor central angle is about 27 degrees.
(220) Example 20. The poly-phase switched reluctance motor assembly of any one of Examples 1-19 wherein each of the stator teeth comprises teeth tips.
(221) Example 21. A stator assembly for a poly-phase switched reluctance motor comprising
(222) a plurality of stator teeth separated by stator slots and surrounding a central bore,
(223) a plurality of coils that are configured in a distributed winding configuration, the plurality of coils includes a coil group for each phase of the poly-phased switched reluctance motor,
(224) wherein the central bore is configured to receive a rotor assembly having a plurality of poles and a total number of stator slots is a multiple of number of phases and number of rotor poles of the motor.
(225) Example 22. The stator assembly according to Example 21, wherein each of the stator slots comprises a coil segment of one of the coils of the plurality of coils.
(226) Example 23. The stator assembly according to any one of Examples 21-22, wherein each coil group comprises at least one coil.
(227) Example 24. The stator assembly according to any one of Examples 21-23, wherein a width of each of the stator teeth of the plurality of stator teeth is less than a width of a rotor pole.
(228) Example 25. The stator assembly according to any one of Examples 21-24, wherein the distributed winding configuration comprises a plurality of phases with at least one phase of the plurality of phases comprising a plurality of coil winding groups.
(229) Example 26. The stator assembly according to any one of Examples 21-25 wherein rotor poles of the received rotor assembly have widths that are equal.
(230) Example 27. The stator assembly according to any one of Examples 21-26 wherein each stator tooth width is equal.
(231) Example 28. The stator assembly according to any one of Examples 21-27, wherein the total number of stator slots comprises a further multiple of a winding distribution parameter such that the total number of stator slots satisfies an equation consisting of:
Total number of stator slots=number of phases×number of rotor poles×winding distribution parameter.
(232) Example 29. The stator assembly according to any one of Examples 21-28, wherein each of the coil segments for a coil group are uniformly distributed between the stator slots.
(233) Example 30. The stator assembly according to any one of Examples 21-29, having an inductance ratio of less than 3.
(234) Example 31. The stator assembly according to Example 30, wherein the inductance ratio is between 2 and 2.5.
(235) Example 32. The stator assembly according to any one of Examples 21-31, wherein the stator has an outer diameter less than 50 mm.
(236) Example 33. The stator assembly according to Example 32, wherein the stator has an outer diameter less than or equal to 45 mm.
(237) Example 34. The stator assembly of any one of Examples 21-33 wherein the stator assembly and rotor assembly are configured to have a difference between a stator central angle and a rotor central angle in a difference range of 5 to 30 degrees.
(238) Example 35. The stator assembly of Example 34 wherein the difference between the stator central angle and the rotor central angle is about 27 degrees.
(239) Example 36. The stator assembly of any one of Examples 21-35 wherein each of the stator teeth comprises teeth tips.
(240) Example 37. A positive airway pressure device comprising a poly-phase switched reluctance motor according to any one of Examples 1-20 configured to provide a supply of pressurized breathable gas.
(241) Example 38. A system for treating a respiratory disorder comprising:
(242) a therapy device comprising a poly-phase switched reluctance motor according to any one of Examples 1-20 configured to provide a supply of pressurized breathable gas;
(243) an air delivery conduit; and
(244) a patient interface configured to receive the supply of pressurized gas from the therapy device via the air delivery conduit and deliver the supply of pressurized gas to a patient.
(245) Example 39. The system according to Example 38 further comprising a humidifier configured to humidify the supply of pressurized gas.
(246) Example 40. A method of controlling a switched reluctance motor, the switched reluctance motor comprising at least three phases, the method comprising:
(247) during each conduction period energizing a first phase with a negative direction current, energizing a second phase with a positive current and having at least one non-energized phase; and
(248) during each commutation period switching off one of the first phase or the second phase to a non-energized state and switching on one of the non-energized phases to an energized state with a same direction current as the first or second phase that was switched off.
(249) Example 41. The method according to Example 40, wherein the switched reluctance motor includes a distributed winding configuration.
(250) Example 42. The method of any one of Examples 40-41 wherein the switched reluctance motor has a total number of stator slots that is a multiple of number of phases and number of rotor poles.
(251) Example 43. The method of Example 42 wherein the total number of stator slots further comprises a multiple of a winding distribution parameter.
(252) Example 44. The method of any one of Examples 40-43 wherein the switched reluctance motor has a stator assembly and rotor assembly configured to have a difference between a stator central angle and a rotor central angle in a difference range of 5 to 30 degrees.
(253) Example 45. The method of Example 44 wherein the difference between the stator central angle and the rotor central angle is about 27 degrees.
(254) Example 46. The method of any one of Examples 40-45 wherein the switched reluctance motor has a plurality of stator teeth, each comprising teeth tips.
(255) Example 47. The method of any one of Examples 40-46 wherein the switched reluctance motor has only three phases.
(256) Example 48. The method of any one of Examples 40-47 wherein the switched reluctance motor is a component of a therapy device configured to supply pressurized gas.
(257) It is therefore to be understood that numerous modifications may be made to the illustrative embodiments and that other arrangements may be devised without departing from the spirit and scope of the technology.