Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Process and system for facilitating chemical identification in detector

A technology for chemical substances and detection parameters, which is used in the calibration of instruments, instruments, measuring devices, etc., and can solve the problem of ions not being completely resolved.

Inactive Publication Date: 2017-08-01
SMITHS DETECTION WATFORD LTD
View PDF3 Cites 1 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0010] However, it has been found that a problem with the use of PCE as a dopant in negative mode IMS detectors is that it interacts with O in the reaction region. 2 – interacts with free electrons, resulting in the production of two different reactant ions, Cl – and Cl – .OOH
However, when the moisture level in the drift region is high, and depending on the environmental conditions, it has been found that these two ions are not thoroughly resolved in the IMS spectrum

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Process and system for facilitating chemical identification in detector
  • Process and system for facilitating chemical identification in detector
  • Process and system for facilitating chemical identification in detector

Examples

Experimental program
Comparison scheme
Effect test

Embodiment Construction

[0027] exist figure 1 In the example shown in , the first part 101 of the method involves the ionization of a sample containing or consisting essentially of isoflurane in a PCE-doped IMS detector to form the PCE-associated reactant ion Cl – and Cl – .OOH. Isoflurane, whose chemical structure is shown below, is known for its use as an anesthetic, is frequently used in veterinary anesthesia, and usually exists as a racemic mixture of (R) and (S) optical isomers .

[0028]

[0029] Isoflurane is particularly advantageous for its PCE-related reactant ion Cl – and Cl – .OOH reacts with both without significant bias towards producing distinct isoflurane monomer ions. Thus, a sample containing or consisting essentially of isoflurane is introduced into a PCE-doped IMS detector, which reacts with the PCE-associated Cl- and Cl-.OOH reactant ions present in the reaction zone to be ionized. After ionization, isoflurane forms a negative monomer ion. The negative isoflurane monom...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

No PUM Login to View More

Abstract

The present disclosure relates to a process for facilitating the identification of target chemicals which may be detected by means of an ion mobility spectrometer and a system for implementing the same. In an aspect of the disclosure, there is provided a process for determining the ratio of CI" to CI".OOH reactant ion species formed in a pentachloroethane doped ion mobility spectrometer operating in negative mode, said process comprising: i) introducing a sample comprising or consisting essentially of isoflurane into a pentachloroethane doped ion mobility spectrometer; ii) collecting data relevant to the detection of two isoflurane monomer ions formed following reaction with CI" and CI".OOH reactant ion species present in the pentachloroethane doped ion mobility spectrometer; and iii) determining the ratio of CI" to CI".OOH reactant ion species formed in the pentachloroethane doped ion mobility spectrometer based on an evaluation of the data collected.

Description

technical field [0001] The present invention relates to methods for facilitating the identification of target chemical species that can be determined by means of ion mobility spectrometry. More specifically, the present invention relates to a method involving the use of isoflurane to facilitate the identification of target chemical species in a sample that is doped with pentachloroethane using a negative mode ion mobility spectrometer (pentachloroethane doped negative mode ion mobility spectrometer ) for analysis. Background technique [0002] Ion mobility spectrometry (IMS) is an analytical technique capable of separating gas-phase ions based on the ratio of ion size to charge caused by the ion-carrier gas interaction in an electric field. IMS is capable of identifying chemical species based on the ionized chemical species passing through a drift chamber separating the ionizer and detector. The output of the IMS detector can be visualized as a "mobility spectrum" plotted ...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
IPC IPC(8): G01N27/62
CPCG01N27/622G01N33/0057H01J49/0009
Inventor I·普罗奇诺P·D·阿诺德
Owner SMITHS DETECTION WATFORD LTD
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products