Patent classifications
G01N24/08
METHOD AND APPARATUS FOR HIGH-THROUGHPUT NUCLEAR MAGNETIC RESONANCE MEASUREMENTS ON BOREHOLE MATERIALS
A method for NMR measurements on borehole materials, e.g., sidewall cores, is based on performing a standard measurement in substantially homogeneous magnetic fields with a sensitivity volume covering an entire sample and a measurement on a fragment of the sample (local measurement), the fragment having a predetermined volume independent of the irregularities of the sample shape (e.g., irregular shaped edges). The fragment of the sample is selected using a switchable static magnetic field gradient or a localized radio-frequency magnetic field. The homogeneous and the local measurement data are processed jointly to obtain volume normalized NMR relaxation data (in porosity units), the processing also using a calibration sample data. A measurement apparatus with an automated sample transfer can be used to implement the method in order to perform high-throughput NMR relaxation measurements that do not require independent measurement of the sample volume.
Metabolomics profiling of central nervous system injury
A method of diagnosing central nervous system injuries such as acquired brain injury (ABI) and/or acquired spinal cord injury (ASI), including mild TBI (concussion or blast wave), mild ASI (contusion, stretch or partial cord transection), non-TBI brain injury and/or non-TSI spinal cord injury in a subject (animal or human). The method includes (a) obtaining a biological test sample from the subject, identifying metabolites in the subject's sample using metabolomics thereby obtaining a subject's metabolite matrix and generating a subject's profile using the patient's metabolite matrix; and (b) using multivariate statistical analysis and machine learning to compare the subject's profile with predetermined set of profiles of CNS injuries and a predetermined set of profiles of controls to determine if the subject has a CNS injury.
Methods and systems for characterizing properties of reservoir rock
Methods and systems are provided that combine NMR and IR spectroscopy measurements on a rock sample to determine data representing at least one property of the rock sample. In one embodiment, cuttings can be split into first and second lots. Results of an NMR measurement performed on the first lot of cuttings without cleaning can be analyzed to determine pore volume of the cuttings. Results of an IR spectroscopy measurement performed on the second lot of cuttings after solvent cleaning can be analyzed to determine matrix density of the cuttings. Porosity can be determined from the pore volume and matrix density of the cuttings. In another embodiment, combined NMR and IR spectroscopy measurements can be performed on an unprepared rock sample (without solvent cleaning) to characterize properties of kerogen in the rock sample and porosity. In another aspect, a method is provided that employs multi-nucleic NMR measurements to determine porosity.
DIGITAL RETORT MEASUREMENT SYSTEMS AND METHODS
Tools and methods are used to determine the oil, water, and solids volume fractions in a drilling fluid at the rig site. The volume fractions can be determined in-line with returned drilling fluid by using an NMR magnet and a flow line or sample chamber that receives a fluid sample and loads it into the NMR magnet. Using an RF probe, spectrometer, and computing device, data processing and interpretation of NMR data from the spectrometer is performed, while also raising a flag when iron contamination exceeds a predefined threshold.
Method for comprehensively characterizing lower limit of oil accumulation of deep marine carbonate reservoir
A method, system and device for comprehensively characterizing a lower limit of oil accumulation of a deep marine carbonate reservoir is provided, aiming to solve the problem that the prior art cannot: accurately determine the lower limit of oil accumulation of the deep marine carbonate reservoir, which leads to the difficulty in predicting and identifying deep effective reservoirs. The method includes: determining lower limit porosity and permeability for oil accumulation based on a boundary line; determining lower limit porosity and permeability for oil accumulation based on a movable oil ratio of a core sample; determining a lower limit pore throat radius for oil accumulation based on a mercury injection experiment; and comprehensively characterizing the lower limit of oil accumulation of a deep marine carbonate reservoir to be predicted. The method, system and device can predict and identify deep effective reservoirs.
METHOD, DEVICE, AND SYSTEM FOR DETECTING SWEETNESS OF FRUIT, AND STORAGE MEDIUM
A method (100), a device (400), and a system for detecting the sweetness of fruit, and a storage medium. The method (100) comprises: using magnetic resonance diffusion weighted imaging to acquire an apparent diffusion coefficient (ADC) of fruit to be detected when same is undamaged (S110); determining an effective ADC of said fruit according to the ADC of said fruit (S120); and determining the sweetness of said fruit according to the effective ADC (S130). The ADC of fruit to be detected may be acquired on the basis of magnetic resonance imaging when said fruit is undamaged, and the ADC is used to determine the sweetness of the fruit, thus achieving non-destructive and reliable fruit sweetness detection.
METHOD, DEVICE, AND SYSTEM FOR DETECTING SWEETNESS OF FRUIT, AND STORAGE MEDIUM
A method (100), a device (400), and a system for detecting the sweetness of fruit, and a storage medium. The method (100) comprises: using magnetic resonance diffusion weighted imaging to acquire an apparent diffusion coefficient (ADC) of fruit to be detected when same is undamaged (S110); determining an effective ADC of said fruit according to the ADC of said fruit (S120); and determining the sweetness of said fruit according to the effective ADC (S130). The ADC of fruit to be detected may be acquired on the basis of magnetic resonance imaging when said fruit is undamaged, and the ADC is used to determine the sweetness of the fruit, thus achieving non-destructive and reliable fruit sweetness detection.
PH-SENSOR
The present disclosure relates to a pH-sensor for determining and/or monitoring a pH value of a medium, having a sensor unit with a wall in contact with the medium, and at least one pH-sensitive material, which has at least one spin state that changes as a function of a pH value. The at least one pH-sensitive material is arranged in or on a region of the wall in such a way that the at least one spin state is subjected to a change in the pH value of the medium. The pH-sensor also includes a spin-sensitive unit, which is configured to detect a variable associated with the at least one spin state, wherein the spin-sensitive unit is arranged in an environment of the at least one pH-sensitive material such that the spin-sensitive unit is subjected to a change in the spin state of the at least one pH-sensitive material.
PH-SENSOR
The present disclosure relates to a pH-sensor for determining and/or monitoring a pH value of a medium, having a sensor unit with a wall in contact with the medium, and at least one pH-sensitive material, which has at least one spin state that changes as a function of a pH value. The at least one pH-sensitive material is arranged in or on a region of the wall in such a way that the at least one spin state is subjected to a change in the pH value of the medium. The pH-sensor also includes a spin-sensitive unit, which is configured to detect a variable associated with the at least one spin state, wherein the spin-sensitive unit is arranged in an environment of the at least one pH-sensitive material such that the spin-sensitive unit is subjected to a change in the spin state of the at least one pH-sensitive material.
METHOD FOR CONDUCTING SOLID STATE NMR ON MACROMOLECULE-CONTAINING SOLID STATE FORMULATIONS
Disclosed herein is a method of conducting direct detection .sup.1H solid state NMR (“ssNMR”) on a macromolecule-containing solid state formulation. The method includes conducting a .sup.1H spin-lattice relaxation time (“T.sub.1”) experiment on the solid state formulation at various temperatures to generate a T.sub.1 value at each temperature, converting the T.sub.1 values to .sup.1H spin-lattice relaxation rate (“R.sub.1”), and plotting R.sub.1 versus temperature to generate a relaxation rate curve for the solid state formulation. The relaxation rate curve can be analyzed to determine the molecular mobility of the macromolecule in the solid state formulation, the degree of aggregation in the solid state formulation, and/or the stability of the solid state formulation.