Abstract:
A method and apparatus are described that permit an analyte concentration to be estimated from a measurement in the presence of compounds that interfere with the measurement. The method reduces the error in the analyte concentration in the presence of interferents. The method includes the use of a set of measurements obtained for a large population having a range of known analyte and interfering compound concentrations. From a sample measurement, which may or may not be one of the population, likely present interferents are identified, and a calibration vector is calculated.
Abstract:
A measuring device for determining the concentration of such gas components from a gas mixture, which includes collision dilation of the absorption lines constituting the absorption spectral bands for measuring objects. The device comprises a non-dispersive concentration measuring sensor (20), which includes: a measuring chamber (6) containing a gas mixture to be analyzed; a radiation source (17) for emitting over a wavelength range which includes an absorption spectral band used in concentration determination; a detector (18) receiving radiation that has passed through the measuring chamber and for producing a first signal (7) therefrom; as well as an optical bandpass filter (16) positioned between the detector and the radiation source. The measuring device further comprises a second measuring sensor (4) for identifying the viscosity or some other viscosity-related feature of a gas mixture to be analyzed and for producing a second signal (9). Both signals (7, 9) are delivered to a calculating unit (8), which uses at least a second signal for performing the corrections required for the first signal. In addition, the device is provided with a display means (10).
Abstract:
A method and apparatus for the determination of spectral samples is disclosed wherein spectral measurements are taken, normalization of the spectral measurements takes place, and a bilinear modeling is performed to extract spectral data. Once this data is derived, the interference quantitization levels are determined using multiple linear regression analysis, and are then removed from the sample readings in order to determine a more precise level of analyte spectra, such as analyte levels of glucose in serum or whole blood.
Abstract:
A method is disclosed of making an on-line gas analysis of a multicomponent gas emission flow by (a) continuously sequestering a sample flow from the gas emission flow, which sample flow may be filtered to substantially eliminate solid or liquid particles, diluted to lower its dew point to below room temperature, and changed in either temperature and/or pressure to be substantially the same in temperature and pressure as that of gases used to create reference transmission frequency spectral data employed in step (d); (b) continuously irradiating the sample flow with an electromagnetic radiation beam while modulating the amplitude of infrared frequencies in the audio frequency range of the beam, either prior to or immediately subsequent to irradiation of the sample flow, to produce electromagnetic signals having discernible amplitude variations resulting from spectral interference patterns; (c) detecting and collecting the signals at a sufficiently high rate to substantially completely distinguish between adjacent spectral pattern amplitude peaks without mutual spectral interference and to permit analysis of the signals in real time; and (d) analyzing the signals in real time by (i) mathematically manipulating the signals in accordance with Beer's Law to create reformed background-corrected data, and (ii) applying reference transmission frequency spectral data to the reformed data for each suspected gaseous component to give a linear quantitative measure of the presence of each and every suspected gas component in the gas emission flow.
Abstract:
A non-dispersive infrared gas analyzer is disclosed that accurately measures the concentration levels of a plurality of gases within a gas mixture. The analyzer includes first and second sample cells and is utilized advantageously for the measurement of NO.sub.x and hydrocarbon gas present in the exhaust of an automobile engine. The gas mixture of the exhaust is chilled before entering the first sample cell to remove a substantial amount of the water vapor from that sample cell to facilitate measurement of the NO.sub.x gas. The second sample cell receives the gas mixtue in an unchilled state to allow for accurate measurement of the hydrocarbon gas. The analyzer includes processors which are utilized to further correct the NO.sub.x measurement and which also interact with each other to provide an output data stream that is representative of the concentration levels of the gases that are being analyzed.
Abstract:
A gas analyzer for performing gas analysis on a sample gas containing contaminants which normally interfere with the operation of the analyzer is disclosed comprising a source of radiant energy; means for directing radiant energy through a sample gas; a disposable gas cell; a detector for receiving radiant energy; and a circuit for analyzing the output of the detector and indicating the concentration of predetermined constituents in the sample gas. The gas cell comprises a disposable sample gas cell having a sample enclosure for containing a sample gas volume; sample windows defining a portion of a sample gas optical path extending from the source of radiant energy through the sample gas volume to the detector; an inlet for supplying sample gas to the sample gas volume and an outlet for exhausting sample gas from the sample gas volume. The disposable sample cell is provided with inlet and exhaust manifolds having cross-sectional areas that minimize dead space and insure laminar flow, minimizing stagnant areas. Specifically, the cross-sectional areas of the inlet and outlet manifolds are relatively constant, the cross-sectional area of the outlet being larger than the cross-sectional area of the inlet, and the inlet and outlet manifolds vary in cross-sectional shape from elongate shapes proximate the windows to a shape having roughly equilateral dimensions distal to the windows. The analyzer and the gas cell are provided with a number of inter-related features that make the analyzer self aligning and eliminates the necessity of recalibrating the analyzer each time a sample cell is replaced.
Abstract:
A method and system for correcting the effect of intensity fluctuations of the transmitted light in an absorption spectroscopy system used for the detection or measurement of chemical species in a medium, whereby one or more modulation bursts are imposed onto a light beam that passes through the medium. This burst signal may be obtained by modulating the bias current of a tunable diode laser, and the modulation burst signal may be optimally at the second harmonic of the modulation frequency of a wavelength modulated beam to allow usage of the same signal path processing used for the spectroscopic detection of the measurand for a second harmonic detection system. The burst signal can be controlled using a smooth window function to minimise the effects of non-linear perturbations that are inherent in tunable diode laser wavelength modulation spectroscopy systems, of optical interference fringes (etalons) and of the residual light absorption by background chemical species or the measurand at the wavelength coinciding with the modulation burst.
Abstract:
A method of determining a concentration of a gas in a sample and/or of the composition of a gas by means of a spectrometer includes measuring an absorption signal of the gas as a function of the wavelength. The wavelength substantially continuously runs through a wavelength range and is superimposed by a harmonic wavelength modulation, wherein the influence of the wavelength modulation on the absorption signal via the light source modulation properties and the detection properties of the spectrometer is dependent on the device properties of the respective spectrometer. The method includes converting the absorption signal into at least one first derivative signal; deriving a gas concentration measurement parameter from the first derivative signal; determining the concentration and/or composition of the gas from at least the gas concentration measurement parameter and from a calibration function compensating for influences of state variables of the gas and of the spectrometer properties.
Abstract:
A differential absorption spectrum for a reactive gas in a gas mixture can be generated for sample absorption data by subtracting background absorption data set from the sample absorption data. The background absorption data can be characteristic of absorption characteristics of the background composition in a laser light scan range that includes a target wavelength. The differential absorption spectrum can be converted to a measured concentration of the reactive gas using calibration data. A determination can be made whether the background composition has substantially changed relative to the background absorption data, and new background absorption data can be used if the background composition has substantially changed. Related systems, apparatus, methods, and/or articles are also described.
Abstract:
A method and apparatus are described that permit an analyte concentration to be estimated from a measurement in the presence of compounds that interfere with the measurement. The method reduces the error in the analyte concentration in the presence of interferents. The method includes the use of a set of measurements obtained for a large population having a range of known analyte and interfering compound concentrations. From a sample measurement, which may or may not be one of the population, likely present interferents are identified, and a calibration vector is calculated.