System for minimizing electrical discharge during ESI operation

Patent metadata

Field	Value
Publication number	US-10818486-B2
Application number	US-201616062936-A
Country	US
Kind code	B2
Filing date	Dec 8, 2016
Priority date	Dec 18, 2015
Publication date	Oct 27, 2020
Grant date	Oct 27, 2020

Abstract

Methods and systems are provided for reducing the occurrence of unwanted electrical discharge when operating an electrospray ion source to generate ions for mass spectrometric analysis. In accordance with various aspects of the applicant's teachings, the methods and systems described herein can provide for controlling the ion emission current so as to limit the onset of avalanche of electrical discharge between the electrospray electrode and the counter electrode under ionization conditions that typically tend to increase the likelihood of such discharge (arcing), while nonetheless providing for maximal ionization efficiency. In various aspects, emission currents between the electrospray electrode and the counter electrode through which the ions are transmitted to a downstream mass analyzer can be maintained at elevated levels, below 10 μA, for example, without the electric potential between the electrospray electrode and the counter electrode initiating the electrical discharge avalanche that results from the dielectric breakdown of the air gap therebetween, which can cause sputtering and effect the long-term operation of the ESI source.

First claim

What is claimed is:

1. An electrospray ion source assembly for generating ions for analysis by a mass spectrometer, comprising:
an ion source housing defining an ionization chamber, the ionization chamber configured to be disposed in fluid communication with a sampling orifice of a mass spectrometer system, the sampling orifice formed in a counter electrode;
at least one heater for heating the ionization chamber;
an electrospray electrode defining an axial bore therethrough for transmitting a liquid sample received from a sample source at an inlet end of the electrospray electrode to an outlet end for discharging the liquid sample from the electrospray electrode into the ionization chamber;
a power source configured to provide an electrical voltage to an electrical circuit containing the electrospray electrode and the counter electrode so as to generate an ion emission current between the electrospray electrode and the sampling orifice as at least a portion of the liquid sample is ionized upon being discharged from the electrospray electrode; and
the ion emission current configured to limit the onset of electrical discharge between the electrospray electrode and the counter electrode without substantially altering the electrical voltage provided to the electrical circuit by the power source, by:
a shunt electrode disposed between an LC column and the outlet end of the electrospray electrode, the shunt electrode configured to be in electrical communication with the liquid sample, wherein at least a portion of the electrical current between the power source and the electrospray electrode is diverted to the shunt electrode based on the conductivity of the portion of the liquid sample between the outlet end of the electrospray electrode and the shunt electrode.

2. The electrospray ion source assembly of claim 1 , wherein the shunt electrode comprises a plurality of shunt electrodes disposed at different distances upstream from the inlet end of the electrospray electrode, wherein one of the plurality of the shunt electrodes is selectively grounded based on the conductivity of the liquid sample.

3. The electrospray ion source assembly of claim 1 , wherein the electrospray electrode comprises a metallized silica capillary.

4. The electrospray ion source assembly of claim 3 , wherein the shape of the outlet end of the electrospray electrode is controlled so as to reduce the electric field thereat.

5. The electrospray ion source assembly of claim 1 , wherein the ion emission current is below about 10 μA.

6. The electrospray ion source assembly of claim 1 , wherein the ion emission current is in a range of about 0.5 μA to about 10 μA.

7. The electrospray ion source assembly of claim 1 , wherein a flow rate of the liquid sample in the electrospray electrode is maintained in a range of less than 1 mL/min.

8. The electrospray ion source assembly of claim 1 , wherein the power source is configured to provide a DC voltage in a range of about 2000 V to about 6000 V to the electrospray electrode.

9. A mass spectrometer system, comprising:
a liquid chromatography (LC) column for providing a liquid sample to be analyzed;
an electrospray ion source in fluid communication with the LC column, the electrospray ion source comprising:
an ion source housing defining an ionization chamber;
at least one heater for heating the ionization chamber;
an electrospray electrode defining an axial bore therethrough for transmitting a liquid sample received from a sample source at an inlet end of the electrospray electrode to an outlet end for discharging the liquid sample from the electrospray electrode into the ionization chamber; and

a mass analyzer for analyzing the ions generated by the ion source, wherein the ions are received by the mass analyzer through a sampling orifice in a counter electrode, the sampling orifice being in fluid communication with the ionization chamber;
a power source configured to provide an electrical voltage to an electrical circuit containing the electrospray electrode and the counter electrode so as to generate an ion emission current between the electrospray electrode and the sampling orifice as at least a portion of the liquid sample is ionized upon being discharged from the electrospray electrode; and
the ion emission current configured to prevent arcing between the electrospray electrode and the counter electrode without substantially altering the electrical voltage provided to the electrical circuit by the power source, by:
a shunt electrode disposed between the LC column and the outlet end of the electrospray electrode, the shunt electrode configured to be in electrical communication with the liquid sample, wherein at least a portion of the electrical current between the power source and the electrospray electrode is diverted to the shunt electrode based on the conductivity of the portion of the liquid sample between the outlet end of the electrospray electrode and the shunt electrode.

10. The mass spectrometer system of claim 9 , wherein ion emission current is below about 10 μA without substantially altering the voltage provided by the power source.

11. A method for operating an electrospray ion source of a mass spectrometer system, the method comprising:
transmitting a liquid sample from an inlet end of an electrospray electrode to an outlet end of the electrospray electrode, the outlet end being disposed in an ionization chamber so as to discharge the liquid sample from the outlet end of the electrospray electrode into the ionization chamber, the ionization chamber being in fluid communication with a sampling orifice formed in a counter electrode of a mass spectrometer system;
heating the ionization chamber;
operating a power source to provide an electrical voltage (electromotive force) to an electrical circuit containing the electrospray electrode and the counter electrode so as to generate an ion emission current between the electrospray electrode and the sampling orifice as at least a portion of the liquid sample is ionized upon being discharged from the electrospray electrode; and
controlling the ion emission current so as to limit the onset of electrical discharge between the electrospray electrode and the counter electrode without substantially altering the electrical voltage provided to the electrical circuit by the power source, by:
providing a shunt electrode disposed between an LC column and the outlet end of the electrospray electrode, the shunt electrode configured to be in electrical communication with the liquid sample, wherein at least a portion of the electrical current between the power source and the electrospray electrode is diverted to the shunt electrode based on the conductivity of the portion of the liquid sample between the outlet end of the electrospray electrode and the shunt electrode.

12. The method of claim 11 , wherein controlling the ion emission current comprises adjusting a distance between the shunt electrode and the electrospray electrode, wherein the distance is based on the conductivity of the liquid sample.

13. The method of claim 11 , wherein the ion emission current is maintained in a range of about 0.5 μA to about 10 μA.

14. The method of claim 11 , wherein the electrospray electrode comprises a metallized silica capillary.

15. The method of claim 11 , wherein the shape of the outlet end of the electrospray electrode is controlled so as to reduce the electric field thereat.

16. The method of claim 11 , wherein a flow rate of the liquid sample in the electrospray electrode is maintained in a range of less than 1 mL/min.

Assignees

• Dh Technologies Dev Pte Ltd

Inventors

• Corr John J
• Covey Thomas R
• Kovarik Peter

Classifications

• H01J49/0477

  using a hot fluid · CPC title

• G01N30/7266

  by electric field, e.g. electrospray · CPC title

• H01J49/044

  with means for preventing droplets from entering the analyzer; Desolvation of droplets · CPC title

• G01N30/72

  Mass spectrometers {(mass spectrometers per se H01J49/00)} · CPC title

• H01J49/165 Primary

  Electrospray ionisation · CPC title