Chemical calibration method and system
View Patent ↗An explosive and narcotics detection system using an ion mobility spectrometer detects the presence of vapor or trace particles of target chemicals. The calibration of the spectrometer depends in part on the stability of a calibrant chemical that may be periodically injected together with sample gas into the ionization region of the spectrometer. The calibrant chemical produces a signal with a drift time that is known relative to target chemicals and may be used to calibrate the expected target chemical drift times. A new calibrant chemical, 5-nitrovanillin, is disclosed for this purpose.
1. A method for calibrating drift time for an ion mobility spectrometer that is open to the atmosphere, the ion mobility spectrometer including a gas ionization region with a sample gas inlet tube and sample gas outlet tube open to the atmosphere, a drift region with an inlet and outlet for a drift gas flow and pneumatically coupled to the ionization region, a charge collecting surface at the end of the drift region opposite the ionization region, and an electric field generator for providing an electric field between said ionization region and said charge collecting surface in order to transport ions in between, the method comprising:
heating a solid phase sample of a calibrant chemical to produce a calibrant gas using a temperature controlled oven in pneumatic communication with said ionization region, wherein said calibrant chemical includes 5-nitrovanillin, also known as 4-hydroxy-3-methoxy-5-nitrobenzaldehyde, CAS number 6635-20-7;
determining the drift time of ions of said calibrant chemical through said ion mobility spectrometer; and
determining the expected drift time of a target chemical using a pre-determined ratio of the reduced mobilities of said target chemical and said calibrant chemical.
2. The method of claim 1 , wherein said temperature-controlled oven is operated at a temperature between 40 degrees Celsius and the melting point of 5-nitrovanillin.
3. The method of claim 1 , wherein said calibrant gas is injected into said ionization region using a carrier gas including at least one of pressurized ambient air and pressurized dry air.
4. The method of claim 1 , wherein said solid phase sample of calibrant chemical has a purity greater than 90%.
5. The method of claim 1 , wherein said drift time is determined based on the difference in the ion charge arrival time at said charge collecting surface and the time of either a pulsed ionization event or the opening of an electronic ion gate.
6. The method of claim 1 , wherein said drift time is discarded if an amplitude of calibrant chemical ion charge is less than 1% of a possible full scale detection amplitude or greater than 30% of the possible full scale detection amplitude.
7. The method of claim 1 , wherein said drift time is discarded if an ion charge peak corresponding to lactic acid or oxide derivatives thereof appears in the spectrum of drift time with an amplitude greater than half the amplitude of the ion charge peak corresponding to 5-nitrovanillin.
8. A system for calibrating drift time, comprising:
an ion mobility spectrometer that is open to the atmosphere, the ion mobility spectrometer including a gas ionization region with a sample gas inlet tube and sample gas outlet tube open to the atmosphere, a drift region with an inlet and outlet for a drift gas flow and pneumatically coupled to the ionization region, a charge collecting surface at the end of the drift region opposite the ionization region, and an electric field generator for providing an electric field between said ionization region and said charge collecting surface in order to transport ions in between;
a temperature controlled oven in pneumatic communication with said ionization region that heats a solid phase sample of a calibrant chemical to produce a calibrant gas, wherein said calibrant chemical includes 5-nitrovanillin, also known as 4-hydroxy-3-methoxy-5-nitrobenzaldehyde, CAS number 6635-20-7; and
an analysis unit that determines the drift time of said calibrant chemical through said ion mobility spectrometer and determines the expected drift time of a target chemical using pre-determined ratio of the reduced mobilities of said target chemical and said calibrant chemical.
9. The system of claim 8 , wherein said temperature-controlled oven is operated at a temperature between 40 degrees Celsius and the melting point of 5-nitrovanillin.
10. The system of claim 8 , wherein said calibrant gas is injected into said ionization region using a carrier gas including at least one of pressurized ambient air and pressurized dry air.
11. The system of claim 8 , wherein said solid phase sample of calibrant chemical has a purity greater than 90%.
12. The system of claim 8 , wherein said drift time is determined based on the difference in the ion charge arrival time at said charge collecting surface and the time of either a pulsed ionization event or the opening of an electronic ion gate.
13. The system of claim 9 , wherein said drift time is discarded if the amplitude of calibrant chemical ion charge is less than 1% of the possible full scale detection amplitude or greater than 30% of the possible full scale detection amplitude.
14. The system of claim 9 , wherein said drift time is discarded if an ion charge peak corresponding to lactic acid or oxide derivatives thereof appears in the spectrum of drift time with an amplitude greater than half the amplitude of the ion charge peak corresponding to 5-nitrovanillin.
15. A method for calibrating drift time for an ion mobility spectrometer that is open to the atmosphere, comprising:
heating a solid phase sample of a calibrant chemical to produce a calibrant gas using a temperature controlled oven in pneumatic communication with an ionization region of the ion mobility spectrometer, wherein said calibrant chemical includes 5-nitrovanillin;
determining the drift time of said calibrant chemical through said ion mobility spectrometer; and
determining the expected drift time of a target chemical using a pre-determined ratio of the reduced mobilities of said target chemical and said calibrant chemical.
16. The method of claim 15 , wherein said temperature-controlled oven is operated at a temperature between 40 degrees Celsius and the melting point of 5-nitrovanillin.
17. The method of claim 15 , wherein said calibrant gas is injected into an ionization region of the ion mobility spectrometer using a carrier gas including at least one of pressurized ambient air and pressurized dry air.
18. The method of claim 15 , wherein said solid phase sample of calibrant chemical has a purity greater than 90%.
19. The method of claim 15 , wherein said drift time is determined based on the difference in the ion charge arrival time at a charge collecting surface of the ion mobility spectrometer and the time of either a pulsed ionization event or the opening of an electronic ion gate.
20. The method of claim 15 , wherein said drift time is discarded if an amplitude of calibrant chemical ion charge is less than 1% of a possible full scale detection amplitude or greater than 30% of the possible full scale detection amplitude.
21. The method of claim 15 , wherein said drift time is discarded if an ion charge peak corresponding to lactic acid or oxide derivatives thereof appears in the spectrum of drift time with an amplitude greater than half the amplitude of the ion charge peak corresponding to 5-nitrovanillin.