Patent application number | Description | Published |
20100002207 | LITHOGRAPHIC APPARATUS AND DEVICE MANUFACTURING METHOD - A lithographic apparatus includes a projection system configured to project an image onto a substrate, a substrate table configured to support the substrate, a first chamber that at least partially surrounds the projection system, and a second chamber that at least partially surrounds the substrate table and a first frame. The apparatus includes a base frame configured to support the second chamber, and an intermediate frame coupled to the base frame. The intermediate frame is configured to separate the first chamber and the second chamber. The apparatus includes a support coupled to the first frame. The support is configured to support the first chamber through a coupled opening in the intermediate frame and the second chamber. | 01-07-2010 |
20100290015 | EX-SITU REMOVAL OF DEPOSITION ON AN OPTICAL ELEMENT - A collector assembly with a radiation collector, a cover plate and a support member connecting the radiation collector to the cover plate are provided. The cover plate is designed to cover an opening in a collector chamber. The collector chamber opening may be large enough to pass the radiation collector and the support member. The removed radiation collector can be cleaned with different cleaning procedures, which may be performed in a cleaning device. Such cleaning device may for example consist of the following: a circumferential hull designed to provide an enclosure volume for circumferentially enclosing at least the radiation collector; an inlet configured to provide at least one of a cleaning gas and a cleaning liquid to the enclosure volume to clean at least said radiation collector; and an outlet configured to remove said at least one of said cleaning gas and said cleaning liquid from the enclosure volume. | 11-18-2010 |
20120140196 | EX-SITU REMOVAL OF DEPOSITION ON AN OPTICAL ELEMENT - A collector assembly with a radiation collector, a cover plate and a support member connecting the radiation collector to the cover plate are provided. The cover plate is designed to cover an opening in a collector chamber. The collector chamber opening may be large enough to pass the radiation collector and the support member. The removed radiation collector can be cleaned with different cleaning procedures, which may be performed in a cleaning device. Such cleaning device may for example consist of the following: a circumferential hull designed to provide an enclosure volume for circumferentially enclosing at least the radiation collector; an inlet configured to provide at least one of a cleaning gas and a cleaning liquid to the enclosure volume to clean at least said radiation collector; and an outlet configured to remove said at least one of said cleaning gas and said cleaning liquid from the enclosure volume. | 06-07-2012 |
Patent application number | Description | Published |
20150125010 | STEREO WIDENING OVER ARBITRARILY-CONFIGURED LOUDSPEAKERS - A system and method are disclosed for effective and simple stereo widening over arbitrarily-configured speakers and its real-time implementation. According to one embodiment, the system includes five processing units: (1) elevation processing unit; (2) side signal or difference signal processing unit; (3) center signal processing unit; (4) binaural signal processing unit; and (5) stereo limiter (to prevent the clipping) unit. Any of the five processing units may be included or omitted depending on the application. In general, embodiments of the present invention provide effective and simple stereo widening schemes with good audio quality results, but without having substantial requirements on the speakers' positional configuration. For example, the proposed schemes can apply to both symmetric and non-symmetric stereo loudspeakers. | 05-07-2015 |
20150126255 | UNIVERSAL RECONFIGURABLE ECHO CANCELLATION SYSTEM - A universal reconfigurable system and method are provided for reducing nonlinear echo and residual echo, and for echo leakage prevention in various time-varying and complex environments is proposed in this invention. According to one embodiment an echo cancellation system includes (1) an adaptive linear filter implemented in either time-domain or frequency-domain; (2) a nonlinear echo suppression; (3) echo leakage prevention; (4) direct current (DC), low frequency residual echo and noise reduction; (5) time-domain nonlinear processor (NLP) to reduce the residual echo; and (6) frequency-domain NLP to further reduce the residual echo. The echo cancellation system is universally applicable to acoustic echo cancellation (AEC) and/or electrical echo cancellation applications. In terms of AEC, this invention is reconfigurable for one or more microphones and/or one or more reference channels. The numbers of microphones and reference channels are user configurable. | 05-07-2015 |
20150146890 | ADAPTIVE BASS PROCESSING SYSTEM - An effective and simple psychoacoustic bass generation system generates a harmonic signal having inter-modulation controllable to remain below a threshold level and includes a high-pass filter configured to pass harmonics which are reproducible with fidelity by the loudspeaker or other transducer and a loudness matching block configured to compensate the loudness of the desired harmonics to match the loudness of the original signal. | 05-28-2015 |
Patent application number | Description | Published |
20080208018 | Apparatuses for Noninvasive Determination of in vivo Alcohol Concentration using Raman Spectroscopy - Methods and apparatuses for the determination of an attribute of the tissue of an individual use non-invasive Raman spectroscopy. For example, the alcohol concentration in the blood or tissue of an individual can be determined non-invasively. A portion of the tissue is illuminated with light, the light propagates into the tissue where it is Raman scattered within the tissue. The Raman scattered light is then detected and can be combined with a model relating Raman spectra to alcohol concentration in order to determine the alcohol concentration in the blood or tissue of the individual. Correction techniques can be used to reduce determination errors due to detection of light other than that from Raman scattering from the alcohol in the tissue. Other biologic information can be used in combination with the Raman spectral properties to aid in the determination of alcohol concentration, for example age of the individual, height of the individual, weight of the individual, medical history of the individual and his/her family, ethnicity, skin melanin content, or a combination thereof. The method and apparatus can be highly optimized to provide reproducible and, preferably, uniform radiance of the tissue, low tissue sampling error, depth targeting of the tissue layers or sample locations that contain the attribute of interest, efficient collection of Raman spectra from the tissue, high optical throughput, high photometric accuracy, large dynamic range, excellent thermal stability, effective calibration maintenance, effective calibration transfer, built-in quality control, and ease-of-use. | 08-28-2008 |
20080319286 | Optical Probes for Non-Invasive Analyte Measurements - An optical probe for non-invasively measuring an analyte property in a biological sample of a subject, comprises a plurality of illumination fibers that deliver source light from an optical probe input to a sample interface, a plurality of collection fibers that deliver light returned from the sample interface to an optical probe output, and wherein the illumination and collection fibers are oriented substantially perpendicular to the sample interface and the illumination and collection fibers are stacked in a plurality of linear rows to provide a stack of fibers arranged in a rectangular pattern. The optical probe is amenable to manufacturing on a scale consistent with a commercial product. | 12-25-2008 |
20090003764 | Method of Making Optical Probes for Non-Invasive Analyte Measurements - An optical probe for non-invasively measuring an analyte property in a biological sample of a subject, comprises a plurality of illumination fibers that deliver source light from an optical probe input to a sample interface, a plurality of collection fibers that deliver light returned from the sample interface to an optical probe output, and wherein the illumination and collection fibers are oriented substantially perpendicular to the sample interface and the illumination and collection fibers are stacked in a plurality of linear rows to provide a stack of fibers arranged in a rectangular pattern. The optical probe is amenable to manufacturing on a scale consistent with a commercial product. Methods of making such probes are described. | 01-01-2009 |
20090234204 | Methods for Noninvasive Determination of in vivo Alcohol Concentration using Raman Spectroscopy - Methods and apparatuses for the determination of an attribute of the tissue of an individual use non-invasive Raman spectroscopy. For example, the alcohol concentration in the blood or tissue of an individual can be determined non-invasively. A portion of the tissue is illuminated with light, the light propagates into the tissue where it is Raman scattered within the tissue. The Raman scattered light is then detected and can be combined with a model relating Raman spectra to alcohol concentration in order to determine the alcohol concentration in the blood or tissue of the individual. Correction techniques can be used to reduce determination errors due to detection of light other than that from Raman scattering from the alcohol in the tissue. Other biologic information can be used in combination with the Raman spectral properties to aid in the determination of alcohol concentration, for example age of the individual, height of the individual, weight of the individual, medical history of the individual and his/her family, ethnicity, skin melanin content, or a combination thereof. The method and apparatus can be highly optimized to provide reproducible and, preferably, uniform radiance of the tissue, low tissue sampling error, depth targeting of the tissue layers or sample locations that contain the attribute of interest, efficient collection of Raman spectra from the tissue, high optical throughput, high photometric accuracy, large dynamic range, excellent thermal stability, effective calibration maintenance, effective calibration transfer, built-in quality control, and ease-of-use. | 09-17-2009 |
20100010325 | System for Noninvasive Determination of Analytes in Tissue - An apparatus and method for noninvasive determination of analyte properties of human tissue by quantitative infrared spectroscopy to clinically relevant levels of precision and accuracy. The system includes subsystems optimized to contend with the complexities of the tissue spectrum, high signal-to-noise ratio and photometric accuracy requirements, tissue sampling errors, calibration maintenance problems, and calibration transfer problems. The subsystems can include an illumination/modulation subsystem, a tissue sampling subsystem, a data acquisition subsystem, a computing subsystem, and a calibration subsystem. The invention can provide analyte property determination and identity determination or verification from the same spectroscopic information, making unauthorized use or misleading results less likely than in systems that use separate analyte and identity determinations. The invention can be used to control and monitor individuals accessing controlled environments. | 01-14-2010 |
Patent application number | Description | Published |
20110178420 | METHODS AND APPARATUSES FOR IMPROVING BREATH ALCOHOL TESTING - Some embodiments of the present invention provide methods and apparatuses for improving the performance and utility of breath alcohol measurements through the use of multivariate spectroscopy. In some embodiments, the spectroscopic breath measurement can be combined with multivariate spectroscopic tissue alcohol and/or tissue biometric measurements in order to overcome the limitations encountered by existing breath alcohol measurement devices. | 07-21-2011 |
20110282167 | SYSTEM FOR NONINVASIVE DETERMINATION OF ALCOHOL IN TISSUE - An apparatus and method for non-invasive determination of attributes of human tissue by quantitative infrared spectroscopy to clinically relevant levels of precision and accuracy. The system includes subsystems optimized to contend with the complexities of the tissue spectrum, high signal- to-noise ratio and photometric accuracy requirements, tissue sampling errors, calibration maintenance problems, and calibration transfer problems. The subsystems include an illumination/modulation subsystem, a tissue sampling subsystem, a calibration maintenance subsystem, an FTIR spectrometer subsystem, a data acquisition subsystem, and a computing subsystem. | 11-17-2011 |
20120078473 | Apparatus and Method for Controlling Operation of Vehicles or Machinery by Intoxicated or Impaired Individuals - The present invention discloses apparatuses and methods for non-invasive determination of attributes of human tissue by quantitative infrared spectroscopy. The embodiments of the present invention include subsystems optimized to contend with the complexities of the tissue measurements. The subsystems can include an illumination/modulation subsystem, a tissue sampling subsystem, a calibration maintenance subsystem, a data acquisition subsystem, and a computing subsystem. Embodiments of the present invention provide analyte property determination and identity determination or verification from the same spectroscopic information, making unauthorized use or misleading results less likely that in systems that include separate analyte and identity determinations. The invention can be used to prevent operation of automobiles or other equipment unless the operator has an acceptable alcohol concentration, and to limit operation of automobiles or other equipment to authorized individuals who are not intoxicated or drug-impaired. | 03-29-2012 |
20130110311 | SYSTEM FOR NONINVASIVE MEASUREMENT OF AN ANALYTE IN A VEHICLE DRIVER | 05-02-2013 |
Patent application number | Description | Published |
20130317328 | Methods and Apparatuses for Noninvasive Determination of in vivo Alcohol Concentration using Raman Spectroscopy - Methods and apparatuses for the determination of an attribute of the tissue of an individual use non-invasive Raman spectroscopy. For example, the alcohol concentration in the blood or tissue of an individual can be determined. A portion of the tissue is illuminated with light, which propagates into the tissue where it is Raman scattered. The Raman scattered light is detected and can be combined with a model relating Raman spectra to alcohol concentration to determine the alcohol concentration in the blood or tissue. Correction techniques can reduce determination errors due to detection of light other than that from Raman scattering from the alcohol in the tissue. Other biologic information can be used with the Raman spectral properties to aid in the determination of alcohol concentration, for example age, height, weight, medical history and his/her family, ethnicity, skin melanin content, or a combination thereof. The method and apparatus can be optimized to provide reproducible and uniform radiance of the tissue, low tissue sampling error, depth targeting of the tissue layers or sample locations that contain the attribute of interest, efficient collection of Raman spectra, optical throughput, photometric accuracy, large dynamic range, thermal stability, calibration maintenance, calibration transfer, built-in quality control, and ease-of-use. | 11-28-2013 |
Patent application number | Description | Published |
20140155760 | REMOTE AND LOCAL TRANSFER OF INFORMATION IN NONINVASIVE HYDRATION MEASUREMENTS - An apparatus and method for non-invasive determination of hydration, hydration state, total body water, or water concentration by quantitative spectroscopy. The system includes subsystems optimized to contend with the complexities of the tissue spectroscopy, high signal-to-noise ratio and photometric accuracy requirements, tissue sampling errors, calibration maintenance, and calibration transfer. The subsystems include an illumination subsystem, a tissue sampling subsystem, a spectrometer subsystem, a data acquisition subsystem, a computing subsystem, and a calibration subsystem. The system can include a plurality of measurement devices, configured to communicate with each other and with a remote receiver or centralized server. The invention contemplates novel ways to arrange various subsystems and to provide operability and communication among them. | 06-05-2014 |
20140171759 | NONINVASIVE DETERMINATION OF INTRAVASCULAR AND EXCTRAVASCULAR HYDRATION USING NEAR INFRARED SPECTROSCOPY - An apparatus and method for non-invasive determination of hydration, hydration state, total body water, or water concentration by quantitative spectroscopy. The system includes subsystems optimized to contend with the complexities of the tissue spectroscopy, high signal-to-noise ratio and photometric accuracy requirements, tissue sampling errors, calibration maintenance, and calibration transfer. The subsystems include an illumination subsystem, a tissue sampling subsystem, a spectrometer subsystem, a data acquisition subsystem, a computing subsystem, and a calibration subsystem. | 06-19-2014 |
20150160121 | Calibration Transfer and Maintenance in Spectroscopic Measurements of Ethanol - Methods of producing a plurality of spectroscopic measurement devices, comprising producing a calibration model that includes the expected range of measurement variation across the plurality of devices; producing the devices; installing the calibration model on each device. Most standard methods focus on ways to reduce the number of replicate samples that are required to be taken on a given instrument or class of instruments. The present methods can reduce that number to zero by anticipating the expected range of instrument variation in manufacturing in the field. This can be important when measuring live biological samples as it is impractical to maintain standard humans, cells, etc. This is in contrast to measurements on dry agricultural products where a standard, sealed dry sample can be maintained for months/years when required. | 06-11-2015 |