The present disclosure provides methods of identifying or certifying an animal that consumed a traceable diet comprising a C.sub.1 metabolizing microorganism.

The present invention relates to a method for determining the origin of glutamic acid in a sample and, in a broader sense, relates to a method for determining the origin of an amino acid. The present invention makes it possible to measure the stable isotope ratio, with a considerably higher accuracy than that of conventional methods, by measuring the δ13C of glutamic acid (amino acid) by elemental analysis-stable isotope ratio mass spectrometry (EA-IRMS) and measuring the δ15N by gas chromatography-stable isotope ratio mass spectrometry (GC-IRMS). In addition, the present invention makes it possible to determine the origin of glutamic acid (amino acid) by comparing the stable isotope ratio of the glutamic acid (amino acid) whose origin is unclear with the stable isotope ratio of glutamic acid (amino acid) whose origin is clear.

Systems and methods of surface logging a well use a plurality of polymeric taggants distinguishable from each other. The systems and methods can include adding each of the plurality of polymeric taggants in a repeating sequence to a circulating drilling fluid while drilling the well and taking a sample drill cuttings carried by the circulating drilling fluid. The systems and methods can also include measuring concentrations of individual polymeric taggants attached to the drill cuttings in the sample and identifying a depth associated with the sample based on the measured concentrations of individual polymeric taggants and on the sequence.

In a mass spectrometry apparatus, an electric field is applied to an injected specimen to ionize the specimen, and mass spectrometry of the specimen is performed. In an emitter which ionizes the specimen, a flashing process to increase a temperature of the emitter is repeatedly performed at a short-time interval during an injection period of the specimen. A flashing current controller controls a flashing current value to be applied to the emitter to increase, in a long term, a flashing temperature which the emitter reaches in the flashing process.

A method of performing mass spectrometry includes accumulating, over an accumulation time, ions produced from components eluting from a chromatography column and transferring the accumulated ions to a mass analyzer. During an acquisition, a mass spectrum of detected ions derived from the transferred ions is acquired. An elution profile is obtained from a series of acquired mass spectra including the acquired mass spectrum and a plurality of previously-acquired mass spectra. The elution profile includes a plurality of detection points representing intensity of the detected ions as a function of time. A current signal state of the elution profile is classified based on a subset of detection points included in the plurality of detection points. The accumulation time for a next acquisition of a mass spectrum is set based on the classified current signal state of the elution profile.

A system for separation of components of a natural gas product uses a first separation column to receive the natural gas product and to provide first stage components including a first component gas, uses a gas converter to provide second stage components that includes third component gas from at least a second component gas of such first stage components, and uses a second separation column to provide third stage components that includes the first component gas, the third component gas, and one or more additional carbon-based components provided in or over a period of time associated with the separation of the components of the natural gas product.

A polyhydric phenol resin is provided. The polyhydric phenol resin comprises a polyhydric phenol resin component and a first component. When the polyhydric phenol resin is characterized in a high-performance liquid chromatography (HPLC), the first component is eluted at a retention time ranging from 27.1 minutes to 28.0 minutes, and based on the total area of the chromatographic peaks of the polyhydric phenol resin, the area percentage of the chromatographic peak of the first component at the corresponding retention time in the spectrum ranges from 1.0% to 20%.

Provided are ion detectors and systems that may employ such ion detectors such as mass spectrometers and other instruments. The ion detectors include a deflector that serves to generate an electric field with designed shape and strength that causes the ions passing into the detector to move along a deflection path. By selectively deflecting the charged ions from an initial propagation axis, the deflector effectively removes unwanted neutral particles from the ion path and reduces background in the resulting spectra.

A system for separation of components of a natural gas product uses a first separation column to receive the natural gas product and to provide first stage components including a first component gas, uses a gas converter to provide second stage components that includes third component gas from at least a second component gas of such first stage components, and uses a second separation column to provide third stage components that includes the first component gas, the third component gas, and one or more additional carbon-based components provided in or over a period of time associated with the separation of the components of the natural gas product.

A gas chromatograph mass spectrometer includes a separator that separates a sample, and a mass analyzer that performs mass spectrometry on the sample introduced from the separator, the mass analyzer includes a filament and an ionization chamber into which thermal electrons from the filament and the sample from the separator are introduced, and an opening through which the thermal electrons emitted from the filament pass and which is formed in the ionization chamber or in a member arranged between the ionization chamber and the filament has a maximum diameter of less than 3 mm.