Abstract: A therapy system configured to wash out or flush out the oral and/or nasal cavity to reduce the effective dead space and reduce the work of breathing. The system may displace the expired air in the oral and/or nasal cavity with atmospheric air, or air with altered concentrations, for example, increased humidity, or oxygen levels. A sealed oral interface is provided to the mouth of a patient to supply a volume of pressurized gas. A control system to synchronize the supply of pressurized gas with the patients respiratory cycle. The supply of respiratory gas may be provided during only a portion of the respiratory cycle.

Abstract: The present disclosure relates to a composition that includes a first oxide having a phosphate, a ratio of Brønsted acid sites to Lewis acid sites between 0.05 and 1.00, and a total acidity between 50 ?mol/g and 300 ?mol/g, where the phosphate is at least one of a functional group covalently bonded to the first oxide and/or an anion ionically bonded to the first oxide.

Abstract: A therapy system configured to wash out or flush out the oral and/or nasal cavity to reduce the effective dead space and reduce the work of breathing. The system may displace the expired air in the oral and/or nasal cavity with atmospheric air, or air with altered concentrations, for example, increased humidity, or oxygen levels. A sealed oral interface is provided to the mouth of a patient to supply a volume of pressurized gas. A control system to synchronize the supply of pressurized gas with the patients respiratory cycle. The supply of respiratory gas may be provided during only a portion of the respiratory cycle.

Abstract: The present disclosure relates to a composition that includes a first oxide having a phosphate, a ratio of Brønsted acid sites to Lewis acid sites between 0.05 and 1.00, and a total acidity between 50 ?mol/g and 300 ?mol/g, where the phosphate is at least one of a functional group covalently bonded to the first oxide and/or an anion ionically bonded to the first oxide.

Abstract: A respiratory treatment apparatus implements pressure delivery control settings by improved set-up procedures. In such an embodiment, a processor may automate setting of parameters for delivering a controlled flow of breathable gas. Data sets of pressure delivery parameter settings may be associated with one or more respiratory pathology indicators. The respiratory pathology indicators may each represent a different respiratory condition diagnosis. The processor may then prompt for an input of at least one of the respiratory pathology indicators. In response to the input, a particular set of pressure delivery parameter settings associated with the input respiratory pathology indicator may then serve as a basis for setting controls for delivering a controlled flow of breathable gas for respiratory treatment.

Abstract: A device (102) provides respiratory treatment for SDB (including mild OSA) and other respiratory conditions. A flow generator warms and humidifies gas at controlled flow levels. For example, the device (102) delivers breathable gas to the upper airway at flow rates of about 10-35 Liters/minute. Levels of flow rate, temperature and/or humidification of the device any be automatically adjusted in response to the detection of SDB events. The device may aim automatically deliver adjustments of any of the levels in accordance with detected phases of respiratory cycles. In some embodiments, the device automatically delivers distinct levels to either of the nares based on independent control of flow to each nare. A warm-up procedure controls temperature and humidity at a desired target during a ramp-up of flow to the set therapy level. A cool-down procedure controls temperature above the dewpoint to avoid condensation internal to the device and patient interface.

Abstract: A device (102) provides respiratory treatment for SDB (including mild OSA) and other respiratory conditions. A flow generator warms and humidifies gas at controlled flow levels. For example, the device (102) delivers breathable gas to the upper airway at flow rates of about 10-35 Liters/minute. Levels of flow rate, temperature and/or humidification of the device may be automatically adjusted in response to the detection of SDB events. The device may also automatically deliver adjustments of any of the levels in accordance with detected phases of respiratory cycles. In some embodiments, the device automatically delivers distinct levels to either of the nares based on independent control of flow to each nare. A warm-up procedure controls temperature and humidity at a desired target during a ramp-up of flow in the set therapy level. A cool-down procedure controls temperature above the dewpoint to avoid condensation internal to the device and patient interface.

Abstract: A Process for the purification of renewable oils. The process may also be applied to petroleum oils such as used motor oil and the like. The process involves centrifuging the renewable oil in a centrifugal device producing a minimum of 7000 RCF, then contacting the oil with a mixture containing water, a straight chain hydro-treated ester compound, and a phosphate derivative at a minimum temperature of 100° C. for 10 minutes, then raising temperature to approximately between 120° C. and 130° C. to complete reaction. The mixture is then again centrifuged in a centrifugal device producing a minimum of 7000 RCF.

Abstract: A method for determining a location and trajectory for a new wellbore relative to an adjacent wellbore includes: receiving controllable variable data and uncontrollable variable data related to fracturing a formation by a stimulation operation in a first wellbore penetrating the formation; receiving pressure communication event or pressure non-communication event identification data related to identification of a pressure communication event or pressure non-communication event in a second wellbore penetrating the formation in response to the fracturing; extracting features from the controllable and uncontrollable variable data to provide extracted features; detecting a pressure communication event using the extracted features and the pressure communication event or pressure non-communication event identification data using an analytic technique; identifying one or more quantified causes of the detected pressure communication event using an artificial intelligence technique; and determining the location and tr

Abstract: Methods and apparatus for assessing the condition of and treating patients for heart failure by the delivery of continuous positive airway pressure are disclosed. Treatment of obstruction due to reflex vocal cord closure often experienced by heart failure patients is distinguished from treatment of upper airway obstruction typically associated with Obstructive Sleep Disorder. Treatment may also be implemented by delivering synchronized cardiac pressure oscillations superimposed on a respiratory pressure level to provide assistance for the heart. Heart treatment pressure dose indicator may be calculated for prescribing and monitoring the delivery of treatment. The apparatus may also generate data to track heart failure condition that may be indicative of the degree of severity of heart failure based upon breathing patterns to assist in the diagnosis and management of heart failure patients.

Abstract: The present disclosure relates to a composition that includes a first oxide having a phosphate, a ratio of Brønsted acid sites to Lewis acid sites between 0.05 and 1.00, and a total acidity between 50 ?mol/g and 300 ?mol/g, where the phosphate is at least one of a functional group covalently bonded to the first oxide and/or an anion ionically bonded to the first oxide.

Abstract: A device (102) provides respiratory treatment for SDB (including mild OSA) and other respiratory conditions. A flow generator warms and humidifies gas at controlled flow levels. For example, the device (102) delivers breathable gas to the upper airway at flow rates of about 10-35 Liters/minute. Levels of flow rate, temperature and/or humidification of the device may be automatically adjusted in response to the detection of SDB events. The device may also automatically deliver adjustments of any of the levels in accordance with detected phases of respiratory cycles. In some embodiments, the device automatically delivers distinct levels to either of the nares based on independent control of flow to each nare. A warm-up procedure controls temperature and humidity at a desired target during a ramp-up of flow to the set therapy level. A cool-down procedure controls temperature above the dewpoint to avoid condensation internal to the device and patient interface.

Abstract: A projectile includes a body and a power generator secured to the body. The power generator includes a stator and a ring including at least one magnet and extending radially around and freely rotatable about at least a portion of the stator. A power generator for a projectile is also provided.

Abstract: A device (102) provides respiratory treatment for SDB (including mild OSA) and other respiratory conditions. A flow generator warms and humidifies gas at controlled flow levels. For example, the device (102) delivers breathable gas to the upper airway at flow rates of about 10-35 Liters/minute. Levels of flow rate, temperature and/or humidification of the device may be automatically adjusted in response to the detection of SDB events. The device may also automatically deliver adjustments of any of the levels in accordance with detected phases of respiratory cycles. In sane embodiments, the device automatically delivers distinct levels to either of the nares based on independent control of flow to each nare. A warm-up procedure controls temperature and humidity at a desired target during a ramp-up of flow to the set therapy level. A cool-down procedure controls temperature above the dewpoint to avoid condensation internal to the device and patient interface.

Abstract: A computer-implemented method and building automation system, the building automation system including a network of electronic devices connected in electronic communication. The method includes initiating an electronic security scan of the controller. The controller electronically assesses security vulnerabilities of the controller, including identifying one or more of a validation of whether the controller is protected by a firewall or other network security device, identifying which communication ports are open, identifying and verifying an Ethernet and Wi-Fi configuration of the controller, determining whether any routers communicating with the controller are protected by the firewall or other network security device, determining whether the controller is running an up-to-date software or firmware version, and determining a listing of software applications and versions installed on the controller.

Abstract: Systems and methods for automatically generating and providing a compliance notification for a document in response to a compliance request received from an electronic device via a network. A governance system is constructed to communicate with a first governing agent device, a first principal device and a second principal device via the Internet. The first governing agent device provides a first document to the governance system, and the governance system compares the first document with stored permissions and at least one permission generated in real-time by a first personal robot representative. The governance system provides a result of the comparison to the first governing agent device.

Abstract: A device (102) provides respiratory treatment for SDB (including mild OSA) and other respiratory conditions. A flow generator warms and humidifies gas at controlled flow levels. For example, the device (102) delivers breathable gas to the upper airway at flow rates of about 10-35 Liters/minute. Levels of flow rate, temperature and/or humidification of the device may be automatically adjusted in response to the detection of SDB events. The device may also automatically deliver adjustments of any of the levels in accordance with detected phases of respiratory cycles. In some embodiments, the device automatically delivers distinct levels to either of the nares based on independent control of flow to each nare. A warm-up procedure controls temperature and humidity at a desired target during a ramp-up of flow to the set therapy level. A cool-down procedure controls temperature above the dewpoint to avoid condensation internal to the device and patient interface.

Abstract: Devices and systems provide methods for detecting respiratory related effort from movements associated with the head or face. In one embodiment, a strain signal is measured by one or more sensors. A processor may analyze the head strain signal to detect respiratory related effort. Detection of effort may serve as a basis for identifying sleep disordered breathing events. For example, the analysis may serve as part of a detector to identify central or obstructive apneas or central or obstructive hypopneas. Sensors may be integrated with headgear to support them at desired locations of the face or head. Strain from head movement may be detected by measuring, for example, tension of the headgear or force applied against the headgear. The headgear may serve as an independent support for the sensors or as a component of a respiratory treatment apparatus, such as a mask or cannula.

Abstract: A method for controlling operation of a CPAP apparatus. The apparatus has a blower, a patient interface, an air delivery conduit for delivering air from the blower to the patient interface, a sensor for determining the pressure in the patient interface, and a control mechanism that causes air to be delivered at a desired pressure to the patient interface and that detects transitions between inhalation and exhalation of a respiratory cycle of a patient in order to synchronise the blower output with the patient's efforts. In one form the CPAP apparatus provides pressure in accordance with a bi-level waveform with at least one characterising parameter of the waveform being automatically adjusted in accordance with indications of sleep disordered breathing. The indications of sleep disordered breathing can be one or more of snoring, apnea, hypopnea, and flow limitation.

Abstract: Embodiments provide an electrical connector having the ability for a high circuit count. An example electrical connector includes a plurality of contact traces extending along a circumference of a tapered post, on a plurality of respective planes perpendicular to a post axis. The electrical connector also includes a tapered cup positioned over the tapered post, having a plurality of inward facing terminal contacts corresponding to the plurality of contact traces, wherein the terminal contacts are configured to maintain contact as the tapered cup rotates about the post axis.