Tracer gas sensing device comprising a gas discharge cell having cell walls defining a discharge volume and a tracer gas inlet into the discharge volume, an optical spectrometer arrangement having a radiation source on a first side of the discharge cell for emitting radiation into the discharge cell and a radiation detector on a second side of the discharge cell opposite to the first side for detecting radiation which was emitted by the radiation source through the discharge volume, and electrodes on opposing sides of the discharge cell for generating a plasma within the discharge cell, said electrodes being unexposed plasma electrodes. The discharge cell may be a dielectric barrier discharge cell and the electrodes may be powered by an AC power source.

A method and system for testing a liquid sample for an organic compound is disclosed, the method including the steps of collecting the liquid sample from a liquid source; transmitting light having a wavelength of between about 190 nanometers and about 310 nanometers into the liquid sample; measuring absorption/transmission of the light by the organic compound in the liquid sample; and determining a concentration of the organic compound within the liquid sample based on the absorption/transmission of the light by the organic compound. The system can include a spectrophotometer for measuring the absorption of UV light by the organic compound, an ion exchange column for removing ion contaminants from the liquid sample, and a vacuum degasser unit for removing gases and other impurities from the liquid sample.

Disclosed is a method for measuring the absorbance of light of a substance in a solution in a measuring cell, said method comprising the steps of: transmitting a first light beam from a light source towards a beam splitter; dividing the first light beam into a signal light ray and a reference light ray by the beam splitter; modulating the signal light ray; modulating the reference light ray; providing the measuring cell such that the signal light ray passes through the measuring cell; detecting a signal in a detector, which signal is the combined signal intensity of the signal light ray and the reference light ray detected by the detector; performing synchronous detection of the detected signal in order to reconstruct the intensities of the signal light ray and the reference light ray from the combined signal detected by the detector, said synchronous detection being based on the modulation performed to the signal light ray and the reference light ray. Disclosed also is a measuring device for carrying out said method

Highly quantitative methods for determining the concentration of residual phase transfer catalysts (PTCs) in radiotracer or radiopharmaceutical doses are described. The methods comprise mixing aliquots of the doses that can contain residual PTCs with a sodium and/or potassium salt; extracting a residual PTC/salt complex into an organic phase; and detecting the amount of PTC/salt complex in the organic phase. The detecting can involve visual colorimetry or measuring the absorbance or transmittance of the organic phase when the sodium and/or potassium salt comprises a chromophoric ion, or measuring the resistance of the organic phase. Also described are devices for use in performing the methods.

A system for monitoring vibrations in a target region of interest may include a pulsed laser transmitter assembly, interferometric, telescope, and receiver optics, a photo-EMF detector assembly, signal conditioning/processing electronics, and a monitoring circuit/display. The detector assembly, which has a photo-EMF detector and amplifier circuits, generates an output signal indicative of the vibrations. A laser module outputs a source beam at a PRF of at least 2 Hz. A beam splitter device splits the source beam into separate interrogating and reference beams. The mirror directs the reference beam onto the photo-EMF detector for interference with a reflected return signal. The telescope optics generates an amplified return signal, and directs the amplified return signal to the photo-emf detector. The monitoring computer compares the output signal from the signal processor to a baseline to ascertain a difference therebetween, and generates a diagnostic signal indicative of the difference.

A spectrometry device includes a switch and a converter. The switch acquires a first reception signal and a second reception signal that respectively include information relating to an optical spectrum and switches between outputting the first reception signal and outputting the second reception signal based on control by a controller. The converter converts the first reception signal or the second reception signal output from the switch into a digital signal.

A method of detecting a geometrical phase change of an intrinsic property of a molecular isomerization includes a series of steps, such as simulating molecular isomerization of the molecule through application of a single shaped pulse to generate a molecular polarization. The steps include separating the real and imaginary parts of a nonlinear susceptibility in a detected molecular signal by controlling a phase of a reference field. The steps include assigning a phase function to obtain separation of the real and imaginary parts. Furthermore, a broadened vibrational lineshape is calculated. The step of identifying conical intersections also occurs. Various pathways of a wave packet in an excited state potential energy surface is discussed and may include multiple laser pulses and methods of detection. The spectral phase may be used to create interference of the wave packet in the excited state to identify and control a wavepacket's pathway and control photoisomerization.

An indicator and method of use thereof, and indicator system and method of use thereof are provided to determine the degree of an oxidative treatment. An indicator is incorporated into the oxidative treatment. The object and the indicator are subjected to the oxidative treatment. A discoloration of the indicator occurs based on an oxidation of the polymer by a process condition of the oxidative treatment oxidizing the polymer. The discoloration of the indicator is measured against a threshold color value to determine the degree of the oxidative treatment.

A method for analyzing a plurality of molecules with cryogenic vibrational spectroscopy including the steps of providing a packet of molecules in a ionized form, injecting the packet into an ion mobility section, spatially separating the ions of the packet into subpackets according to their collisional cross section (CCS), recompressing the subpackets, by removing an empty space between them, loading the ions into a cryogenic ion trap by keeping subpackets with different collisional cross section in a respective separate compartment, cooling the ions in collisions with a buffer gas, tagging the ions by attaching a messenger molecule, sending a pulse to the trap to excite vibrations of the cold, trapped, and messenger-tagged ions, and separately ejecting ion subpacket from the trap into an extraction region of a time-of-flight mass spectrometer and measuring the number of remaining messenger-tagged ions and untagged ions for each subpacket.

An object of the present invention is to provide a curcumin-containing preparation that enables efficient curcumin ingestion. The object is achieved by a curcumin-containing preparation comprising amorphous curcumin and being substantially free of crystalline curcumin, wherein, in an infrared absorption spectrum with curve fitting by a Voigt function, a ratio (Cp/Ap) is 0.25 or less, the ratio (Cp/Ap) being a ratio of peak intensity Cp having the maximum in the range of 1508.00 to 1513.00 cm.sup.1 to peak intensity Ap having the maximum in the range of 1513.50 to 1517.00 cm.sup.1.