49353 results about "Humidity" patented technology

Embodiments of the present invention provide a unique surgical handpiece having improved operation, durability and reliability. In one embodiment, the present invention provides a motorized handheld surgical instrument having one or more sensors for sensing motion, position, pressure, humidity, and various other environmental conditions relevant to the operation and maintenance of the surgical instrument.

A control system for automatically detecting moisture on the windshield of a vehicle. The automatic moisture detecting system includes an optical system for imaging a portion of the windshield on to an image array sensor, such as a CMOS active pixel sensor. The voltages of each of the pixels which represents the illumination level is converted to a corresponding gray scale value by an analog digital converter. The gray scale values corresponding to the image are stored in memory. The spatial frequency composition of the gray scale values are analyzed to determine the amount of rain present. In order to provide a control signal to control the operation of the windshield wipers of the vehicle as a function of the amount of moisture present. The system is also adapted to detect the level of fog both on the interior of the windshield as well as the exterior of the windshield. By providing a system for automatically detecting the presence of fog on the interior and exterior of the windshield, serious performance limitations of known automatic rain sensors are eliminated.

A fuel cell gas management system including a cathode humidification system for transferring latent and sensible heat from an exhaust stream to the cathode inlet stream of the fuel cell; an anode humidity retention system for maintaining the total enthalpy of the anode stream exiting the fuel cell equal to the total enthalpy of the anode inlet stream; and a cooling water management system having segregated deionized water and cooling water loops interconnected by means of a brazed plate heat exchanger.

A system and method for detecting, monitoring and analyzing physiological characteristics. Signals from a subject are acquired from a suite of sensors, such as temperature, carbon dioxide, humidity, light, movement, electromagnetic and vibration sensors, in a passive, non-invasive manner. The signals are processed, and physiological characteristics are isolated for analysis. The system and method are to analyze sleep patterns, as well as to prevent bed sores or detect conditions such as illness, restless leg syndrome, periodic leg movement, sleep walking, or sleep apnea. However, numerous other applications of the invention are also disclosed.

A humidifier and humidity sensor for use with a breathing assistance apparatus. The humidity sensor senses absolute humidity, relative humidity and/or temperature at both the patient end and humidifier end. The humidifier may also include provision to both control independently the humidity and temperature of the gases. Further, a chamber manifold facilitates easy connection of the humidifier to various outlets, inlets and sensors. A heated conduit provides a more effective temperature profile along its length.

Systems and methods for modeling the behavior of an enclosure for use by a control system of an HVAC system are described. A model for the enclosure that describes the behavior of the enclosure for use by the control system is updated based on a weather forecast data. The weather forecast data can include predictions more than 24 hours in the future, and can include predictions such as temperature, humidity and/or dew point, solar output, precipitation. The model for the enclosure can also be updated based on additional information and data such as historical weather data such as temperature, humidity, wind, solar output and precipitation, occupancy data, such as predicted and/or detected occupancy data, calendar data, and data from the one or more weather condition sensors that sense current parameters such as temperature, humidity, wind, precipitation, and/or solar output. The model for the enclosure can be updated based also on an enclosure model stored in a database, and/or on enclosure information from a user. The model can be updated based on active testing of the enclosure which can be performed automatically or in response to user input. The testing can include heating and/or cooling the enclosure at times when the enclosure is not likely to be occupied.

A pressure support system that comprises a patient circuit, a docking assembly, and a tank. The patient circuit delivers a pressurized flow of breathable gas to a patient. The docking assembly has an inlet and an outlet that is adapted to receive the pressurized flow of breathable gas, and is also adapted to be connected with the patient circuit. The tank is constructed and arranged to be removably connected with the docking assembly, and enables the pressurized flow of breathable gas to pass therethrough. The tank is also adapted to contain a liquid such that a humidity level of the pressurized flow of breathable gas is elevated as the pressurized flow of breathable gas passes therethrough.

A humidifier for a respiratory apparatus for delivering a humidified flow of breathable gas to a patient includes a humidifier chamber configured to store a supply of water to humidify the flow of breathable gas, the humidifier chamber comprising a first heating element configured to heat the supply of water; a relative humidity sensor to detect a relative humidity of ambient air and generate signals indicative of the ambient relative humidity; a first temperature sensor to detect a temperature of ambient air and generate signals indicative of the ambient temperature; and a controller configured to determine an absolute humidity of the ambient air from the signals generated by the relative humidity sensor and the first temperature sensor and to control the first heating element to provide a predetermined relative humidity to the flow of breathable gas. A method of humidifying a flow of breathable gas to be provided to a patient includes determining an absolute humidity of ambient air used to form the flow of breathable gas; and controlling a temperature of a supply of water that humidifies the flow of breathable gas to provide a predetermined absolute humidity corresponding to a predetermined temperature and a predetermined relative humidity of the flow to be delivered to the patient.

The present invention relates to a wetness monitoring system that includes a data collection device that sends wetness measurement data to a central computer that detects changes in wetness measurement data caused by the presence of urine or other dielectric fluids. The data collection device includes a semi-reusable sensor and reusable data collector that are worn on a garment of the person. The data collector includes an internal power source so that the person can live a normal ambulatory life. The data collector has an electrical circuit that uses the changing resistance characteristics in the sensor to gather wetness measurement data. The data collector periodically generates and transmits a signal containing the actual wetness measurement data. The signals are coded to identify the particular data collector or person sending the signal. The data collector is programmed to conserve power by sending signals less frequently during periods when the sensor is clearly dry. Signals are sent more frequently when the sensor is damp or a wetness event may have occurred. The central computer receives the signals containing the wetness measurement data and compares the measurement data to an adjustable wetness sensitivity level to determine if a wetness event has occurred. When the central computer determines that a wetness event has occurred, the computer displays the name of the particular person wearing the data collector and the approximate time that the wetness event occurred. The system then pages an appropriate healthcare worker to inform them that the particular individual needs attention and tracks the approximate response times to ensure that the patient is continuously receiving prompt care.

An ambulatory medical device for detecting acceleration, temperature, and/or humidity conditions in or around the medical device is provided. The medical device includes one or more acceleration, thermal, and/or humidity sensors which detect acceleration, temperature, and/or humidity conditions in or around the medical device. In response to detected conditions, the medical device may, among other things, alter the operation of the device, provide an alarm or warning to the user, or transmit data about the detected conditions to another device.

The invention comprises use of Dynamically Switchable Bypass (DSB) elements in association with one or more Light Emitting Diodes (LEDs) in arrays for illumination circuits to provide rugged, reliable lighting. The DSBs are selected from Transient Voltage Suppressors, including Silicon, Metal Oxide Varistors, and Multi Layer Varistors as well as Zener Diodes. The DSBs are not used as circuit protecting devices, but rather as alternative paths for electric current to bypass failed LEDs. Bi-directional TVSs are used as alternative electric paths for circuits using Alternating Current (AC) and parallel LED arrays that light on both phases of AC. Zener Diodes are used in parallel to, but in the opposite polarity orientation to, one or more LEDs in DC or rectified AC circuits. The inventive paired DSB/LED elements overcomes the black-out problems of prior series LED illumination systems, making possible the use of robust LEDs in illumination systems where reliability, long life, low power consumption, low heat output, resistance to shock, vibration, and humidity, and self-diagnosis are important. The DSB elements have breakdown voltages slightly higher than the LED(s) they support, so that when an LED fails, the conduction through the DSB begins. Because the conduction voltage of the DSB so nearly matches the conduction voltage of the LED(s), the remainder of the circuit continues to function as normal. The system is self-diagnostic in that any LED failure presents itself as a dark LED rather than as a whole string of dark LEDs. DSBs may be used with incandescent bulbs.

A method and apparatus for extracting CO₂ from air comprising an anion exchange material formed in a matrix exposed to a flow of the air, and for delivering that extracted CO₂ to controlled environments. The present invention contemplates the extraction of CO2 from air using conventional extraction methods or by using one of the extraction methods disclosed; e.g., humidity swing or electro dialysis. The present invention also provides delivery of the CO₂ to greenhouses where increased levels of CO₂ will improve conditions for growth. Alternatively, the CO₂ is fed to an algae culture.

An improved moisture management system for installation over doors and windows in buildings that included exterior, stucco-covered, curtain walls comprising an integrally formed, three sided, elongated track including a base, an upright front wall that includes at its base weep holes for the removal of entrained moisture as well as a longitudinal forward extending finish stop above the weep holes, and an upright rear wall at opposing elongated edges of the base, and, extending angularly downward from the outside of the base, and integrally formed therewith, a drip plate that permits ready drainage of water exiting the moisture management system through the weep holes in the upright front wall. Preferably, elongated striations in the front faces of both the front and rear upright walls as well as holes in the upright front wall above the finish stop provide improved adherence of sealants and adhesives used in the installation process.

This disposable device for securing an ostomy bag to a stoma created in a patient, of the type comprising means for joining the ostomy bag to an adhesive seal (5) which is applied on the patient via a contact face, a through-passage (8) communicating with the stoma being formed in the adhesive seal (5), of which the contact face on the patient is at least partially covered by an adhesive composition, is characterized in that the adhesive seal (5) additionally comprises means (15, 16, 17, 18, 19) for detecting wetness of the adhesive composition and means for triggering an alarm when a predetermined level of wetness is reached in the adhesive composition.

A container for a product uses a location circuit for determining the location of the container, a storage element for storing a container identification code, a plurality of data acquisition components for acquiring status of at least two characteristics of at least one of the container, the product and a user of the product, and a communication interface for generating and sending a communication signal including (a) the container identification code from the storage element, (b) the location of the container from the location circuit, and (c) the status of the at least two characteristics from the data acquisition components. The container may be an auto-injector for containing a medicament, or a case for containing an item such as an auto-injector. Generally, the location circuit uses the global positioning system (GPS). The data acquisition components are chosen from a camera, and at least one sensor for sensing at least one of a thermal image, vibration, temperature, humidity, a chemical and an audio signal. The characteristic may be use of the product, or lack of use of at least one of the container and the product.

An improved method and an improved instrument for analyte determination that uses infrared radiation naturally emitted by subject are disclosed. The method is based on Thermal Emission Spectroscopy (TES) whereby the spectral signal is measured in reference to a body's physiological and ambient parameters. The instrument that realizes the method incorporates temperature and humidity sensors. Ambient environmental parameters and subject parameters as disclosed allow normalization of spectrally specific analyte signal for grater precision and accuracy of analytes concentration determination. Such improvement leads to a universal calibration in, for example, non-invasive blood glucose measurements in human subjects.