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641 results about "Mass spectrography" patented technology

Mass spectrograph. n. An instrument used to determine the masses of atoms or molecules, in which a beam of charged particles is passed through an electromagnetic field that separates particles of different masses.

Laser desorption ion source

Atmospheric pressure, intermediate pressure and vacuum laser desorption ionization methods and ion sources are configured to increase ionization efficiency and the efficiency of transmitting ions to a mass to charge analyzer or ion mobility analyzer. An electric field is applied in the region of a sample target to accumulate ions generated from a local ion source on a solid or liquid phase sample prior to applying a laser desorption pulse. The electric field is changed just prior to or during the desorption laser pulse to promote the desorption of charged species and improve the ionization efficiency of desorbed sample species. After a delay, the electric field may be further changed to optimize focusing and transmission of ions into a mass spectrometer or ion mobility analyzer. Charged species may also be added to the region of the laser desorbed sample plume to promote ion-molecule reactions between the added ions and desorbed neutral sample species, increasing desorbed sample ionization efficiency and / or creating desired product ion species. The cycling of electric field changes is repeated in a timed sequence with one or more desorption laser pulse occurring per electric field change cycle. Embodiments of the invention comprise atmospheric pressure, intermediate pressure and vacuum pressure laser desorption ionization source methods and devices for increasing the analytical flexibility and improving the sensitivity of mass spectrometric analysis.
Owner:PERKINELMER HEALTH SCIENCES INC +1

Open probe method and device for sample introduction for mass spectrometry analysis

An open probe method for sample introduction into a mass spectrometer is disclosed, comprising the steps of: loading a sample holder with sample compounds to be analyzed; heating a probe oven; introducing said sample compounds in said sample holder into said heated probe oven; flowing inert gas into said heated probe oven; vaporizing said sample in said heated probe oven by the combined effect of oven temperature and inert gas flow; entraining said vaporized sample in said inert gas; and, transferring said vaporized sample in inert gas into an ion source of a mass spectrometer; wherein said heated probe oven remains open to the ambient atmosphere during sample introduction and analysis; said inert gas is flowing in said heated probe oven in two directions of a transfer line to a mass spectrometer ion source and to the oven opening; said vaporized sample in inert gas is transferred through a heated transfer line directly into the ionization chamber of an ion source of a mass spectrometer. An apparatus for this method of sample introduction is also disclosed. The primary advantage of this method and apparatus is that the heated probe oven remains open to the ambient atmosphere during sample introduction and analysis thereby enabling faster sample analysis.
Owner:AMIRAV AVIV

Compositions and methods for analyzing biomolecules using mass spectroscopy

Compositions and methods for mass spectroscopy are disclosed. The compositions and methods relate to the analysis of proteins and other biopolymers using mass spectroscopy, particularly matrix-assisted laser desorption time-of-flight mass spectrometry (MALDI-TOF MS).
Owner:LIFE TECH CORP

Method for detecting volatile organic compound in cigarette filter

The invention provides a method for detecting volatile organic compound in a cigarette filter, which comprises the following steps: a) preparing a sample; b) preparing a matrix correcting agent; c) preparing an interior label solution; d) preparing a standard sample; e) preparing a standard working solution; f) performing detection by using headspace-gas chromatography/ mass-spectrography; and g) calculating a detection result of the volatile organic compound in the sample. The invention establishes the method for detecting the volatile organic compound residue in the cigarette filter for the first time. By using the saturation sodium chloride aqueous solution as the matrix correcting agent and the fluorobenzene as the interior label, the matrix effect of a solid absorption matrix (namely the cigarette filter) is efficiently reduced and the error caused by the poor repeatability of the pre-treatment and the low precision of instrument is reduced. In the whole process, no organic solvent is used. The method has the advantages of environmental friendliness, energy-saving and low consumption. The detecting method has few interference factors and good repeatability, is accurate in measuring result, is simple to operate, and can be used for obviously increasing the sensitivity of headspace analysis.
Owner:ZHENGZHOU TOBACCO RES INST OF CNTC

Laser desorption ion source

Atmospheric pressure, intermediate pressure and vacuum laser desorption ionization methods and ion sources are configured to increase ionization efficiency and the efficiency of transmitting ions to a mass to charge analyzer or ion mobility analyzer. An electric field is applied in the region of a sample target to accumulate ions generated from a local ion source on a solid or liquid phase sample prior to applying a laser desorption pulse. The electric field is changed just prior to or during the desorption laser pulse to promote the desorption of charged species and improve the ionization efficiency of desorbed sample species. After a delay, the electric field may be further changed to optimize focusing and transmission of ions into a mass spectrometer or ion mobility analyzer. Charged species may also be added to the region of the laser desorbed sample plume to promote ion-molecule reactions between the added ions and desorbed neutral sample species, increasing desorbed sample ionization efficiency and / or creating desired product ion species. The cycling of electric field changes is repeated in a timed sequence with one or more desorption laser pulse occurring per electric field change cycle. Embodiments of the invention comprise atmospheric pressure, intermediate pressure and vacuum pressure laser desorption ionization source methods and devices for increasing the analytical flexibility and improving the sensitivity of mass spectrometric analysis.
Owner:PERKINELMER HEALTH SCIENCES INC +1

Electronic cigarette liquid and quality detecting method thereof

The invention relates to electronic cigarette liquid and a quality detecting method. The raw materials of the electronic cigarette liquid are cigarette industry finished cigarette tobacco supercritical fluid extracting substances, other components are added, even mixing is carried out according to weight percentage, and then the liquid is prepared. According to the formula, the liquid comprises 10%-30% of finished cigarette tobacco extracting substances, 5%-15% of tobacco flavor, 2%-10% of deionized water and 10%-30% of glycerine, and the rest is propylene glycol. A gas chromatography-mass spectrography method is used for analyzing the extracting substances, a chromatographic peak area normalization method is used for determining the relative content of various volatile components, and according to the key chemical components which determine characteristic aroma style and the magnitude of the relative content, the quality of the electronic cigarette liquid is evaluated. According to the electronic cigarette liquid, the cigarette finished cigarette tobacco supercritical fluid extracting substances are used as main components, the aroma and the taste of an electronic cigarette are made similar to the taste and sense judgment of a traditional cigarette to the maximum degree, and the problem that single cigarette regulated cigarette liquid taste is single and is not harmonious is solved. Meanwhile, cigarette liquid flavor component evaluation is objective and accurate through the gas chromatography-mass spectrography method.
Owner:CHINA TOBACCO YUNNAN IND

Chromatograph on-line analysis method for source rock by closed ball milling, heating analysis and cold trap trapping

The invention discloses a chromatograph on-line analysis method for source rock by closed ball milling, heating analysis and cold trap trapping, which is used for analyzing light fraction compound and percentage composition thereof in the dispersed organic matter of the source rock, and is characterized by comprising the following steps: carrying out vacuum sealing and ball milling on a source rock sample, carrying out ball milling, crushing, then heating to 300DEG C, and carrying out thermal desorption; blowing the pyrolysed hydrocarbon to a liquid helium cold trap by utilizing helium; placing the cold trap into a chromatograph furnace; and trapping, then carrying out chromatograph or Chromatographic-MS on-line analysis to obtain the qualitative data of chromatograph fine separation and / or Chromatographic-MS analysis of the light fraction in the source rock. The separation degree of the sample can approximate to the separation effect of the light dydrocarbon chromatograph separation of crude oil; the invention has good repeatability, reduces the volatilization loss of the light fraction in the crushing process because of the large volume of the sample before being put in a ball milling tank; and the qualitative analysis result can be used for researching the maturity and the environment of sedimentation of the source rock and carrying out oil source comparison.
Owner:PETROCHINA CO LTD

Mass spectrometric analysis method and system using the method

A tandem analysis system is provided for ionizing a substance, performing mass spectrometric analysis of various ion types generated, selecting and dissociating an ion type, the ion type having a specific mass-to-charge ratio, and thereby, repeating mass spectrometric analysis measurement on the ion of the ion type over n-th stages. A processing judges control content for the analysis next to MSn (the n-th stage mass spectrometric analysis) within a predetermined time, based on ion intensity being represented by an ion peak with respect to the mass-to-charge ratio of each ion in the MSn result. An ion detection unit judges isotope-peak from the measured ionized data. Assuming that the MS1 count number of a parent-ion peptide measured during a certain constant time-interval is I, a data processing unit makes the MS2 integration number-of-times or analysis time of the peptide proportional to 1 / I.
Owner:HITACHI HIGH-TECH CORP

Laser desorption ion source

Atmospheric pressure, intermediate pressure and vacuum laser desorption ionization methods and ion sources are configured to increase ionization efficiency and the efficiency of transmitting ions to a mass to charge analyzer or ion mobility analyzer. An electric field is applied in the region of a sample target to accumulate ions generated from a local ion source on a solid or liquid phase sample prior to applying a laser desorption pulse. The electric field is changed just prior to or during the desorption laser pulse to promote the desorption of charged species and improve the ionization efficiency of desorbed sample species. After a delay, the electric field may be further changed to optimize focusing and transmission of ions into a mass spectrometer or ion mobility analyzer. Charged species may also be added to the region of the laser desorbed sample plume to promote ion-molecule reactions between the added ions and desorbed neutral sample species, increasing desorbed sample ionization efficiency and / or creating desired product ion species. The cycling of electric field changes is repeated in a timed sequence with one or more desorption laser pulse occurring per electric field change cycle. Embodiments of the invention comprise atmospheric pressure, intermediate pressure and vacuum pressure laser desorption ionization source methods and devices for increasing the analytical flexibility and improving the sensitivity of mass spectrometric analysis.
Owner:PERKINELMER HEALTH SCIENCES INC +1

Affinity capture mass spectroscopy with a porous silicon biosensor

Affinity Capture-Mass Spectroscopy (AC-MS), an analytical technique which couples the sensitivity of a label-free binding detected biosensor, and the information richness of mass spectroscopy is described. A 3-dimensional porous silicon bio-surface is used to capture proteins, DNA, or small molecules while acquiring a label-free, time resolved signal linearly proportional to the amount of binding. A switch to dissociative buffer conditions then frees the captured molecule for analysis by mass spectroscopy. In particular, techniques for use with electrospray mass spectroscopy are described.
Owner:SILICON KINETICS
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