Patent application number | Description | Published |
20090015750 | Large scale liquid crystal structures - A liquid crystal structure ( | 01-15-2009 |
20100001795 | Baseband Predistortion Device And Method - The present invention discloses a baseband predistorter and baseband predistortion method. The baseband predistorter comprising: an address generator for calculating an address of a phase basic lookup table and an address of an amplitude basic lookup table; a parameter determining unit for determining a phase translational amount, an amplitude translational amount, a phase curvature adjustment amount and an amplitude curvature adjustment amount; a phase translating unit for changing the address in accordance with the phase translational amount; an amplitude translating unit for changing the address in accordance with the amplitude translational amount; a phase basic lookup table searching section for determining a corresponding phase output; an amplitude basic lookup table searching section, for determining a corresponding amplitude output; a phase curvature adjusting section, for adjusting the phase output; and an amplitude curvature adjusting section, for adjusting the amplitude output. | 01-07-2010 |
20100039100 | Nonlinear Degree Measuring Apparatus And Method For A Power Amplifier, Predistortion Compensation Apparatus - This invention relates to a nonlinear degree measuring apparatus and method for a power amplifier, and a predistortion compensation apparatus. The nonlinear degree measuring apparatus comprises a delayer ( | 02-18-2010 |
20110068868 | Amplifier Device and Predistortion Control Method - This invention relates to an amplifier device and a predistortion control method. The amplifier device comprises a predistortion unit, a predistortion control unit, and an amplifier unit, of which the predistortion control unit controls the predistortion unit in accordance with a signal fed back from the amplifier unit. The predistortion control method comprises determining power of a left side lobe of two side lobes of a frequency spectrum of the signal fed back from the amplifier unit; determining power of a right side lobe of two side lobes of a frequency spectrum of the signal fed back from the amplifier unit; determining a cost function in accordance with the power of the first and right side lobes, and controlling the predistortion unit in accordance with the cost function. | 03-24-2011 |
20110080553 | ELECTRICALLY CONTROLLED MEDIUM FOR MODULATING LIGHT - An electrically controlled medium for modulating light includes two plastic thin film layers ( | 04-07-2011 |
20110187455 | Adaptive Digital Predistortion Device and Method - The present invention relates to an adaptive digital predistortion device and method. The adaptive digital predistortion device comprising: a predistortion unit for predistorting an input signal according to a predistortion parameter stored in a look-up table; a cost function generation unit for generating a cost function; a fixed segment point determination unit for determining a fixed segment point; and an update unit for updating parameters (u | 08-04-2011 |
20130315082 | METHOD AND APPARATUS FOR SEARCHING CARRIER FREQUENCIES - A method and apparatus for searching carrier frequencies (CFs) including determining all CFs to be measured within a frequency band according to a predetermined frequency interval; selecting part of the CFs as Sampling Measurement CFs (SMCFs) according to a predetermined band search step, and for each of the SMCFs, calculating initial peak to average ratio (PAR) of the SMCFs; weighting the initial PAR of each of the SMCFs by using initial PARs of SMCFs left and right neighboring each of the SMCFs, to obtain a determined PAR of each of the SMCFs; ordering the determined PARs of all the SMCFs, and selecting, in a descending order of the determined PARs, a predetermined number of SMCFs and frequencies to be measured left and right neighboring the selected SMCFs as a search result. | 11-28-2013 |
Patent application number | Description | Published |
20080201871 | ANTIMICROBIAL COLORANTS - Quaternary ammonium salts were incorporated into anthraquinone dyes via a stable linkage. The structure of the antimicrobial colorants were characterized by Fourier Transform Infrared (FTIR), Nuclear Magnetic Resonance (NMR) and UV-vis spectrometry. The dyes demonstrated excellent antimicrobial ability against both gram-negative and gram-positive bacteria in aqueous solution, as indicated by very low minimum inhibitory concentration (MIC). The colorants showed excellent stability in water under light, continuous heating as well as acidic and alkaline conditions. | 08-28-2008 |
20090197084 | BIOCIDAL FIBERS - The present invention provides graft biocidal N-halamine polymers. The biocidal polymers are prepared by contacting precursor graft polymers with a halogen source. The precursor graft polymers are prepared by grafting a polymer, such as a polyolefin, with a vinyl monomer under suitable conditions, for example, a reactive extrusion condition. In one embodiment, the graft polymerization is carried out in the presence of a vinyl monomer and a radical initiator. The biocidal polymers have potent antimicrobial activities against a broad spectrum of microorganisms and virus, such as | 08-06-2009 |
20100233458 | THERMOPLASTIC POLYMER MICROFIBERS, NANOFIBERS AND COMPOSITES - The present invention provides methods of making micron, submicron or nanometer dimension thermoplastic polymer microfibrillar composites and fibers, and methods of using the thermoplastic polymer microfibers and nanofibers in woven fabrics, biocidal textiles, biosensors, membranes, filters, protein support and organ repairs. The methods typically include admixing a thermoplastic polymer and a matrix material to form a mixture, where the thermoplastic and the matrix are thermodynamically immiscible, followed by extruding the mixture under conditions sufficient to form a microfibrillar composite containing a plurality of the thermoplastic polymer microfibers and/or nanofibers embedded in the matrix material. The microfibers and/or nanofibers are isolated by removing the surrounding matrix. In one embodiment, the microfibrillar composite formed is further extended under conditions sufficient to form a drawn microfibrillar and/or nanofibrillar composite with controlled diameters. | 09-16-2010 |
Patent application number | Description | Published |
20090299545 | METHOD AND SYSTEM FOR MICROFLUIDIC DEVICE AND IMAGING THEREOF - A biological substrate, e.g., microfluidic chip. The substrate includes a rigid substrate material, which has a surface region capable of acting as a handle substrate. The substrate also has a deformable fluid layer coupled to the surface region. One or more well regions are formed in a first portion of the deformable fluid layer and are capable of holding a fluid therein. The one or more channel regions are formed in a second portion of the deformable fluid layer and are coupled to one or more of the well regions. An active region is formed in the deformable fluid layer. At least three fiducial markings are formed within the non-active region and disposed in a spatial manner associated with at least one of the well regions. A control layer is coupled to the fluid layer. | 12-03-2009 |
20100119154 | IMAGE PROCESSING METHOD AND SYSTEM FOR MICROFLUIDIC DEVICES - A method for processing an image of a microfluidic device. The method includes receiving a first image of a microfluidic device. The first image corresponds to a first state. Additionally, the method includes receiving a second image of the microfluidic device. The second image corresponds to a second state. Moreover, the method includes transforming the first image and the second image into a third coordinate space. Also, the method includes obtaining a third image based on at least information associated with the transformed first image and the transformed second image, and processing the third image to obtain information associated with the first state and the second state. | 05-13-2010 |
20100166608 | METHOD AND SYSTEM FOR MICROFLUIDIC DEVICE AND IMAGING THEREOF - A biological substrate, e.g., microfluidic chip. The substrate includes a rigid substrate material, which has a surface region capable of acting as a handle substrate. The substrate also has a deformable fluid layer coupled to the surface region. One or more well regions are formed in a first portion of the deformable fluid layer and are capable of holding a fluid therein. The one or more channel regions are formed in a second portion of the deformable fluid layer and are coupled to one or more of the well regions. An active region is formed in the deformable fluid layer. At least three fiducial markings are formed within the non-active region and disposed in a spatial manner associated with at least one of the well regions. A control layer is coupled to the fluid layer. | 07-01-2010 |
20120045087 | ANALYSIS ENGINE AND DATABASE FOR MANIPULATING PARAMETERS FOR FLUIDIC SYSTEMS ON A CHIP - Systems for managing workflows to perform chemical or biological reactions using microfluidic devices. | 02-23-2012 |
20120242825 | METHOD AND SYSTEM FOR MICROFLUIDIC DEVICE AND IMAGING THEREOF - A method for producing an image of an object within a chamber of a microfluidic device includes providing the microfluidic device having x, y, and z dimensions and a chamber depth center point located along the z dimension. The chamber depth center point is located a known z dimension distance from a fiducial marking embedded within the microfluidic device. The method also includes placing the microfluidic device within an imaging system that includes an optical device capable of detecting the fiducial marking. The optical device defines an optical path axially aligned with the z dimension and has a focal plane perpendicular to the optical path. When the focal plane is moved along the optical path, the fiducial marking is maximally detected when the focal plane is at the z depth in comparison to when the focal plane is not substantially in-plane with the z depth. | 09-27-2012 |
20120245888 | METHODS AND SYSTEMS FOR IMAGE PROCESSING OF MICROFLUIDIC DEVICES - A method of processing data associated with fluorescent emissions from a microfluidic device. The method includes performing an auto-focus process associated with a first image of the microfluidic device and performing an auto-exposure process associated with the first image of the microfluidic device. The method also includes capturing a plurality of images of the microfluidic device. The plurality of images are associated with a plurality of thermal cycles. The method further includes performing image analysis of the plurality of captured images to determine a series of optical intensities and performing data analysis of the series of optical intensities to provide a series of change in threshold values. | 09-27-2012 |
20130078610 | METHOD AND SYSTEM FOR THERMAL CYCLING OF MICROFLUIDIC SAMPLES - A thermal cycler for a microfluidic device includes a controller operable to provide a series of electrical signals, a heat sink, and a heating element in thermal communication with the heat sink and operable to receive the series of electrical signals from the controller. The thermal cycler also includes a thermal chuck in thermal communication with the heating element. The thermal chuck comprises a heating surface operable to make thermal contact with the microfluidic device. The heating surface is characterized by a temperature ramp rate between 2.5 degrees Celsius per second and 5.5 degrees Celsius per second and a temperature difference between a first portion of the heating surface supporting a first portion of the microfluidic device and a second portion of the heating surface supporting a second portion of the microfluidic device is less than 0.25° C. | 03-28-2013 |
20130266204 | METHOD AND SYSTEM FOR MICROFLUIDIC DEVICE AND IMAGING THEREOF - A biological substrate, e.g., microfluidic chip. The substrate includes a rigid substrate material, which has a surface region capable of acting as a handle substrate. The substrate also has a deformable fluid layer coupled to the surface region. One or more well regions are formed in a first portion of the deformable fluid layer and are capable of holding a fluid therein. The one or more channel regions are formed in a second portion of the deformable fluid layer and are coupled to one or more of the well regions. An active region is formed in the deformable fluid layer. At least three fiducial markings are formed within the non-active region and disposed in a spatial manner associated with at least one of the well regions. A control layer is coupled to the fluid layer. | 10-10-2013 |
20140133732 | METHODS AND SYSTEMS FOR IMAGE PROCESSING OF MICROFLUIDIC DEVICES - A method of processing data associated with fluorescent emissions from a microfluidic device. The method includes performing an auto-focus process associated with a first image of the microfluidic device and performing an auto-exposure process associated with the first image of the microfluidic device. The method also includes capturing a plurality of images of the microfluidic device. The plurality of images are associated with a plurality of thermal cycles. The method further includes performing image analysis of the plurality of captured images to determine a series of optical intensities and performing data analysis of the series of optical intensities to provide a series of change in threshold values. | 05-15-2014 |
20140154787 | METHOD AND APPARATUS FOR BIOLOGICAL SAMPLE ANALYSIS - A method of adjusting amplification curves in a PCR experiment includes receiving a plurality of amplification curves for a sample and computing a first parameter for each of the plurality of amplification curves. The method also includes computing a second parameter for each of the plurality of amplification curves and computing a third parameter using at least a portion of the first or second parameters. The method further includes computing an offset for each of the plurality of amplification curves. The offset is a function of the first parameter and the third parameter. Moreover, the method includes adjusting at least one of the plurality of amplification curves by subtracting the offset. | 06-05-2014 |
Patent application number | Description | Published |
20110185594 | SHOE UPPER, THE METHOD FOR PREPARING THE SAME AND THE USE THEREOF - The present invention pertains to a shoe upper, the method for preparing the same and the use thereof. This invention provides a method for preparing shoe upper by spraying polyurethane reaction system, avoids the complicated steps of cutting, shaping, stitching and bonding, simplify the production process, reduces the equipment requirements, saves cost and improves the production efficiency. | 08-04-2011 |
20130140373 | POLYURETHANE BALLAST LAYER, THE METHOD FOR PREPARING THE SAME AND THE USE THEREOF - The present invention relates to a polyurethane ballast layer, the method for preparing the same and a railway comprising the polyurethane ballast layer. The polyurethane ballast layer provided in this invention comprises a polyurethane-filled ballast layer and a polyurethane external protective layer, wherein the polyurethane-filled ballast layer comprises ballasts and polyurethane foam filled in the space among the ballasts. The polyurethane ballast layer provided in this invention can reduce the probability of ballast crashing, shifting and cracking under heavy load, and separate the ballast track from the outside environment to prevent rain, snow and wastes from entering into the internal space of the ballast track bed. Furthermore, the polyurethane ballast layer can keep the polyurethane foam filled in the ballasts layer away from water in the outside environment to avoid hydrolysis. The polyurethane ballast layer presented in this invention can be used in the railway ballast track bed to extend the track bed maintenance cycle, and save maintenance cost significantly. | 06-06-2013 |
20130335718 | METHOD FOR MEASURING DISTORTION OF PROJECTION OBJECTIVE - A method for measuring distortion of a projection objective, which includes: obtaining a plurality of first positional deviations between two groups of patterns formed respectively after two exposures performed in a same exposure field during a stepping and exposing process of the reticle stage (S | 12-19-2013 |