A method and apparatus is provided for concentration determination of at least one component in an acid catalyst for hydrocarbon conversion containing an unknown concentration of an acid, an acid-soluble-oil (ASO), and water. An instrument configured for measuring a property of the acid catalyst, has responsivities to concentrations of one of the acid, ASO, and water, substantially independent of the concentrations of the others of the acid catalyst, ASO, and water. A temperature detector is configured to generate temperature data for the acid catalyst. A processor is configured to capture data generated by the temperature detector and the instrument, and to use the data in combination with a model to determine a temperature compensated concentration of the one of the acid, the ASO, and the water. Optionally, one or more other instruments configured for measuring other properties of the liquid mixture may also be used.

Techniques for generating magnetic resonance (MR) images of a subject from MR data obtained by a magnetic resonance imaging (MRI) system, the techniques including: obtaining input MR data obtained by imaging the subject using the MRI system; generating a plurality of transformed input MR data instances by applying a respective first plurality of transformations to the input MR data; generating a plurality of MR images from the plurality of transformed input MR data instances and the input MR data using a non-linear MR image reconstruction technique; generating an ensembled MR image from the plurality of MR images at least in part by: applying a second plurality of transformations to the plurality of MR images to obtain a plurality of transformed MR images; and combining the plurality of transformed MR images to obtain the ensembled MR image; and outputting the ensembled MR image.

Explosives concealed within electronic devices, such as smartphones and tablet PCs, are detected using NQR spectroscopy. For example, a suspect electronic device can be placed inside a NQR scanner and be subject to interrogation electromagnetic radiation at varying frequencies. The electronic device is exposed to interrogation electromagnetic radiation at frequencies that correspond to chemical components of various explosives. In the event that an explosive chemical component is present inside the electronic device, irradiating the electronic device with interrogation electromagnetic radiation at the specific NQR frequency of that explosive chemical component will cause the explosive chemical component to emit feedback electromagnetic radiation at that frequency. Consequently, the NQR scanner can measure the feedback electromagnetic radiation and determine that the frequency of the feedback electromagnetic radiation indicates the presence of the explosive chemical component inside the electronic device.

In a method to determine a complete parameter of a pulse sequence composed of multiple pulse sequence modules for operating a magnetic resonance examination apparatus parameter information of the pulse sequence modules is stored in a memory in leaves and nodes of a tree structure, and the parameter information stored in the tree structure is evaluated to determine the complete parameter of the pulse sequence.

In a method to determine a complete parameter of a pulse sequence composed of multiple pulse sequence modules for operating a magnetic resonance examination apparatus parameter information of the pulse sequence modules is stored in a memory in leaves and nodes of a tree structure, and the parameter information stored in the tree structure is evaluated to determine the complete parameter of the pulse sequence.

Systems and methods for magnetic field-dependent relaxometry using magnetic resonance imaging (“MRI”) are provided. Relaxation parameters, including longitudinal relaxation time (“T1”) and transverse relaxation time (“T2”), are estimated from magnetic resonance signal data acquired at multiple different magnetic field strengths using the same MRI system. By measuring these relaxation parameters as a function of magnetic field strength, T1 dispersion data, T2 dispersion data, or both, are generated. Based on this dispersion data, quantitative physiological parameters can be estimated. As one example, iron content can be estimated from T2 dispersion data.

In a magnetic resonance method and apparatus to determine a subject-specific B1 distribution of an examination subject in a measurement volume in the magnetic resonance apparatus, a first measurement data set of the examination subject is acquired using a first pulse sequence, a second measurement data set of the examination subject is acquired using a second pulse sequence, and a third measurement data set of the examination subject is acquired using a third pulse sequence. A first phase is determined from the first measurement data set, a second phase from the second measurement data set and a third phase from the third measurement data set. A relevant phase shift is calculated from the first phase, the second phase and the third phase, and the B1 distribution are determined from the calculated relevant phase shift.

In a magnetic resonance method and apparatus to determine a subject-specific B1 distribution of an examination subject in a measurement volume in the magnetic resonance apparatus, a first measurement data set of the examination subject is acquired using a first pulse sequence, a second measurement data set of the examination subject is acquired using a second pulse sequence, and a third measurement data set of the examination subject is acquired using a third pulse sequence. A first phase is determined from the first measurement data set, a second phase from the second measurement data set and a third phase from the third measurement data set. A relevant phase shift is calculated from the first phase, the second phase and the third phase, and the B1 distribution are determined from the calculated relevant phase shift.

The invention features methods for detecting the hydration state or vascular volume of a subject using a device capable of nuclear magnetic resonance (NMR) measurement. The methods involve exposing a portion of a tissue of the subject in vivo to a magnetic field and RF pulse from the device to excite hydrogen nuclei of water within the tissue portion, and measuring a relaxation parameter of the hydrogen nuclei in the tissue portion, the relaxation parameter being a quantitative measure of the hydration state or vascular volume of the subject as a whole. The invention also features devices and computer-readable storage media for performing the methods of the invention.

A method for determining a B.sub.0 map for, for example, performing an imaging magnetic resonance measurement using a magnetic resonance apparatus, includes measuring an original magnetic field distribution in a measurement volume of the magnetic resonance apparatus, and computing a final B.sub.0 map that describes a magnetic field distribution produced in the measurement volume of the magnetic resonance apparatus by setting a shim state. The magnetic field distribution produced in the measurement volume of the magnetic resonance apparatus by setting the shim state differs from the original magnetic field distribution.