1513 results about "Calibration curve" patented technology

An active-pulse blood analysis system has an optical sensor that illuminates a tissue site with multiple wavelengths of optical radiation and outputs sensor signals responsive to the optical radiation after attenuation by pulsatile blood flow within the tissue site. A monitor communicates with the sensor signals and is responsive to arterial pulses within a first bandwidth and active pulses within a second bandwidth so as to generate arterial pulse ratios and active pulse ratios according to the wavelengths. An arterial calibration curve relates the arterial pulse ratios to a first arterial oxygen saturation value and an active pulse calibration curve relates the active pulse ratios to a second arterial oxygen saturation value. Decision logic outputs one of the first and second arterial oxygen saturation values based upon perfusion and signal quality.

A method is provided for determining optimal stimulus pulsewidth and stimulus amplitude for stimulating nerves with at least one electrode (17). The method comprises: providing a predetermined calibration curve comprising a set of pulsewidth and amplitude values; and delivering sets of pulsewidths and amplitude values which are part of the calibration curve to the at least one electrode (17) to determine at least the optimal pulsewidth. A pulsewidth (70) and an amplitude can be efficiently selected that is efficacious and provides an ample clinical usage range (UR).

A method for determining an unknown starting quantity of a target nucleic acid sequence in a test sample comprises amplifying the unknown starting quantity of the target nucleic acid sequence in the test sample and known starting quantities of a calibration nucleic acid sequence in respective calibration samples; and determining a respective threshold value for each of the nucleic acid sequences using a derivative of a growth curve derived for the sequence. The starting quantity of the target nucleic acid sequence in the test sample is determined using the threshold value determined for the target sequence and a calibration curve derived from the threshold values determined for the known starting quantities of the calibration nucleic acid sequences.

A method for selecting an adjustment for at least one drive voltage used to drive an OLED display to reduce power consumption including operating the display to produce a calibration curve which depicts the drive voltage versus current or luminance, and selecting the adjustment for the drive voltage based upon the calibration curve so as to reduce the power consumed by the OLED display while maintaining desired luminance throughout the lifetime of the OLED display.

The present disclosure includes a pulse oximeter attachment having an accessible memory. In one embodiment, the pulse oximeter attachment stores calibration data, such as, for example, calibration data associated with a type of a sensor, a calibration curve, or the like. The calibration data is used to calculate physiological parameters of pulsing blood.

A method for determining a soluble human ST2 in a sample conveniently at a high sensitivity and an assay kit are provided. By an immunological method comprising a step for bringing a sample into contact with an immobilized antibody formed by binding to an insoluble support a first anti-human ST2 antibody which binds specifically to a non-denatured human ST2, a step for labelling a first reaction product generated in the previous step by reacting said first reaction product with a second anti-human ST2 antibody which binds specifically to a non-denatured human ST2 by recognizing a site different from the site on ST2 where said first anti-human ST2 antibody binds and which is labelled with a label, and a step for determining the amount of the label on said first reaction product which has been labelled, a soluble human ST2 in a sample is determined. In addition, a recombinant ST2 is employed as a standard to prepare a calibration curve, based on which the ST2 in a sample is quantified.

The invention discloses a method for estimating an SOC of a lithium battery. The method comprises the following steps of (S1) obtaining an SOH value of the battery, and determining the current maximum available capacity CN of the battery; (S2) calculating a current SOC value of the battery online by using an ampere-hour integral method; (S3) starting a corresponding offline model parameter according to a sampling temperature T and an estimated value of the current SOC of the battery, and calculating current open-circuit voltage OCV by combining the current sampling current I and terminal voltage U; (S4) obtaining a real value SOC (t)* of the current SOC of the battery according to the estimated value of the current SOC of the battery in the step (S2), the current open-circuit voltage OCV in the step (S3) and an OCV-SOC calibration curve; (S5) correcting the current estimated SOC value of the ampere-hour integral method by using the real value SOC (t)* of the current SOC of the battery, and further carrying out calculation by using the ampere-hour integral method; and (S6) repeating the steps (S3), (S4) and (S5). According to the method, piecewise correction is carried out on a traditional algorithm for estimating the SOC by the ampere-hour integral method, an accumulative error of the ampere-hour integral method is effectively eliminated, and the estimation accuracy of the SOC is improved.

An optical method for measuring the temperature of a substrate material with a temperature dependent band edge. In this method both the position and the width of the knee of the band edge spectrum of the substrate are used to determine temperature. The width of the knee is used to correct for the spurious shifts in the position of the knee caused by: (i) thin film interference in a deposited layer on the substrate; (ii) anisotropic scattering at the back of the substrate; (iii) the spectral variation in the absorptance of deposited layers that absorb in the vicinity of the band edge of the substrate; and (iv) the spectral dependence in the optical response of the wavelength selective detection system used to obtain the band edge spectrum of the substrate. The adjusted position of the knee is used to calculate the substrate temperature from a predetermined calibration curve. This algorithm is suitable for real-time applications as the information needed to correct the knee position is obtained from the spectrum itself. Using a model for the temperature dependent shape of the absorption edge in GaAs and InP, the effect of substrate thickness and the optical geometry of the method used to determine the band edge spectrum, are incorporated into the calibration curve.

What is disclosed is a system and method for image-based determination of concentration of CO and CO₂ in a vehicle's exhaust gas in an emissions testing environment. In one embodiment, the present method involves receiving an IR image of the exhaust plume of a motor vehicle intended to be tested for CO and CO₂ concentrations. The IR image has been captured using a mid-wave infrared camera with at least one optical filter tuned to the infrared absorption band of CO and CO₂. The images are pre-processed to isolate pixels which contain the exhaust plume. The intensity values of pixels in those isolated regions are normalized and concentrations of CO and CO₂ are determined via a calibration curve which relates pixel intensities to concentrations. The concentrations are compared to an emissions standard set for the vehicle to determine whether the vehicle is a gross polluter.

The present invention is an apparatus and method for determining the remaining service life of electrochemical energy generation and storage device including batteries, supercapacitors, DSSC solar cells and fuel cell. Measurements are performed by passing ultrasonic oscillations through the test object. The apparatus of the present invention comprises two arrays of transmitting and receiving ultrasonic probes between which the object being tested is affixed. Polyurethane tips are used for matching the acoustic resistance of the probes with the test object body. The apparatus includes means for positioning the transmitting and the receiving probe arrays relative to each other. The apparatus includes an electromagnetic means for measuring the test object thickness. The calibration characteristic for determining the remaining service life of a the test object are established from the signal values from the ultrasonic probes related to the number of charge-discharge cycles obtained at various charge values. A three-dimensional approximating dependence surface is constructed using the normalized signals from the receiving probes. The average value of this surface is determined. The remaining service life of the test object is determined using a calibration curve based on the average level of the surface

The sample measuring face of a dielectric resonator (20) is placed near a standard sample having a known dielectric constant at a fixed interval D. While appropriately varying the dielectric constant and thickness of the standard sample under the above condition, the variation of the resonance frequency of the dielectric resonator (20) is measured for each varied dielectric constant and thickness to draw a calibration curve of the varied resonance frequency depending on the dielectric constant and thickness. Under the same condition where calibration curve is drawn, the variation of the resonance frequency of the dielectric resonator (20) for a sample having a known thickness is measured. The dielectric constant of the sample is found from the measurement value and the calibration curve. The dielectric constant of not only a sheetlike sample but also a three-dimensional molded article or a liquid sample can be measured easily.

In order to allow detecting backscattered electrons (BSEs) generated from the bottom of a hole for determining whether a hole with a super high aspect ratio is opened or for inspecting and measuring the ratio of the top diameter to the bottom diameter of a hole, which are typified in 3D-NAND processes of opening a hole, a primary electron beam accelerated at a high accelerating voltage is applied to a sample. Backscattered electrons (BSEs) at a low angle (e.g. a zenith angle of five degrees or more) are detected. Thus, the bottom of a hole is observed using “penetrating BSEs” having been emitted from the bottom of the hole and penetrated the side wall. Using the characteristics in which a penetrating distance is relatively prolonged through a deep hole and the amount of penetrating BSEs is decreased to cause a dark image, a calibration curve expressing the relationship between a hole depth and the brightness is given to measure the hole depth.

A probe for measuring the viscosity and/or temperature of high temperature liquids, such as molten metals, glass and similar materials comprises a rod which is an acoustical waveguide through which a transducer emits an ultrasonic signal through one end of the probe, and which is reflected from (a) a notch or slit or an interface between two materials of the probe and (b) from the other end of the probe which is in contact with the hot liquid or hot melt, and is detected by the same transducer at the signal emission end. To avoid the harmful effects of introducing a thermally conductive heat sink into the melt, the probe is made of relatively thermally insulative (non-heat-conductive) refractory material. The time between signal emission and reflection, and the amplitude of reflections, are compared against calibration curves to obtain temperature and viscosity values.

The measurement instrument includes an attribute information output section to output attribute information about the attributes of the measurement instrument as an electric physical value. The attribute information is based on at least one of the conditions including a resistance of the attribute information output section, a location of the attribute information output section, and the size of a region on which the attribute information output section is formed. The attribute information may be used to select the calibration curve suitable for the measurement instrument. The attribute information may be one that relates to a specific measurement standard applied to the measurement instrument.

Method for measuring the global ion concentration of a body fluid that comprises application of a stable DC voltage between first and second electrodes of a cell for measuring the global ion concentration of a body fluid so as to cause electrochemical hydrolysis reactions of the body fluid water to occur at the level of said first and second electrodes, measurement of a hydrolysis current generated by said electrochemical hydrolysis reactions of the water and determination of the global ion concentration of the body fluid by comparison with a previously defined calibration curve. The measuring cell comprises a fluid channel having an internal cross-section smaller than or equal to 1.5 mm.

A system and a method of measuring a particle's size in a select aerosol using the optical diameter of the particle to perform a mobility and/or aerodynamic diameter conversion without any knowledge about the particle's shape and its optical properties in the aerosol being characterized. In one example embodiment of the invention, the method includes generating a set of calibration data and finding the optimal refractive index and shape that best fits the calibration data. In addition, the method includes creating a new calibration curve that provides a mobility-equivalent or aerodynamic-equivalent diameter.

This invention relates to a method of obtaining optimal focus for exposing a photoresist in an EUV lithography with an EUV mask containing a pattern with an assist feature. The invention also relates to an EUV mask with a special focus test target for monitoring focus in EUV lithography, and a method of fabricating this EUV mask by designing the special focus test target. The EUV mask contains a repeating pattern, wherein the repeating pattern has two different pitches, i.e. a first pitch and a second pitch, and contains an assist feature between main features. Because the two different pitches have different focus offsets, the difference between linewidths of said gratings provides a calibration curve which is a measure of focus. The method for monitoring focus is performing an EUV exposure using a focus position with a pre-determined focus position as calibrated using the linewidth difference between the two gratings. The EUV mask for monitoring focus of present invention is applicable to both test and product masks.

The invention relates to the field of two-phase/multi-phase flow measurement, aims to realize the non-intrusive and high precision synchronization acquisition of the flow parameters of a liquid film in (outside) a pipeline and temperature field distribution, and is used for the deep study of a liquid film flow characteristic, a heat transfer characteristic and the like. The employed technical scheme is that according to the liquid film temperature field and flow field simultaneous measurement method based on laser induced fluorescence, when a liquid film with dissolved fluorescent dye forms a dynamic liquid film in a pipeline inner/outer wall or a flat panel, a liquid film fluorescence image is taken through a high speed camera, for a same taken fluorescence image, based on a high speed calibration parameter, the geometric feature of the liquid film fluorescence image is accurately extracted, and flow field characteristics comprising a liquid film thickness and a velocity are obtained. At the same time, based on a calibrated temperature-fluorescence intensity calibration curve, laser intensity calibration and a fluorescence intensity extraction method, a liquid film fluorescence image brightness is accurately extracted, and the instantaneous and time averaged temperature field distribution of the liquid film are obtained. The method is mainly applied to a two-phase/multi-phase flow measurement occasion.

Provided is a polycarbonate-polyorganosiloxane copolymer, including a specific polycarbonate block unit (A) and a specific polyorganosiloxane block unit (B), in which in a differential molecular weight distribution curve obtained from measurement of the polyorganosiloxane block unit (B) by gel permeation chromatography using the polystyrene calibration curve, the curve having an axis of abscissa indicating a logarithmic value log(M) of a molecular weight M and an axis of ordinate indicating dw/d log(M) obtained by differentiating a concentration fraction w with respect to the logarithmic value log(M) of the molecular weight, (1) a dw/d log(M) value becomes maximum in a range of 3.4≦log(M)≦4.0, and (2) in the differential molecular weight distribution curve, a ratio of a value obtained by integrating the dw/d log(M) value over a range of 4.0≦Log(M)≦4.5 to a value obtained by integrating the dw/d log(M) value over the entire range of the log(M) is 6% or more and 40% or less.