IP Library Granted Patent US 11,828,739
Granted Patent B2
US 11,828,739 · App. 17/457,120 · Granted Nov 28, 2023

Large volume gas chromatography injection port

Inventors: Kelly Renee McPartland (West Hartford, CT); Martin L. Spartz (Ellington, CT)
Assignee: MLS ACQ, Inc.
G01N30/74G01J3/42G01N21/3504G01N30/12G01N30/16G01N30/20G01N30/30G01N30/32G01N30/40G01N30/7206G01N2021/3595G01N2030/008G01N2030/025G01N2030/121G01N2030/128G01N2030/328G01N2030/402G01N2030/743
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Quick Facts
Patent No.
US 11,828,739
App. No.
17/457,120
Granted
Nov 28, 2023
Kind
B2
Abstract

A method and system for sample analysis involve a temporally-resolving separation of sample components. In the method, solvent vapors are condensed prior to entering a temporally-resolving separator, a GC column, for example, and solvent-depleted vapors are directed to the separator where constituents are resolved in time. A system for analyzing a sample comprises an injection port, a temporally-resolving separator (e.g., a GC column) and a conduit connecting the two. The injection port is at a temperature sufficiently high to vaporize the solvent and analytes present in a sample. The conduit is configured and/or operated to condense the solvent, while maintaining the analytes in the vapor phase.

Claims (42)

1. A sample analysis method, comprising:

vaporizing a solvent and analytes present in a sample;

condensing solvent vapors upstream of a temporally-resolving separator to produce a solvent-depleted vapor component;

passing the solvent-depleted vapor component through the temporally-resolving separator, thereby resolving in time analytes present in the solvent-depleted vapor component; and

analyzing the time-resolved analytes with a Fourier transform infrared spectrometer.

2. The sample analysis method of claim 1 , further comprising evacuating the condensed solvent vapors.

3. The sample method of claim 1 , wherein the solvent is water and is present in the sample in an amount of at least 99 volume percent.

4. The sample analysis method of claim 1 , wherein the sample is provided by direct injection and without sample splitting.

5. The sample analysis method of claim 1 , wherein the solvent vapor is condensed in a transfer line upstream of the temporally-resolving separator.

6. The sample analysis method of claim 1 , wherein the temporally-resolving separator is a GC column.

7. The sample analysis method of claim 1 , wherein at least a portion of solvent vapors condenses on inner surfaces of a transfer line.

8. A sample analysis method, comprising:

vaporizing a sample containing a solvent and analytes from a thermal desorption tube or a cryo-trap;

condensing solvent vapors upstream of a temporally-resolving separator to produce a solvent-depleted vapor component; and

passing the solvent-depleted vapor component through the temporally-resolving separator, thereby resolving in time analytes present in the solvent-depleted vapor component.

9. The sample analysis method of claim 8 , wherein the method does not employ a secondary thermal desorption tube.

10. The sample analysis method of claim 8 , further comprising a mass spectrometry or an optical spectrometry analyzer.

11. The sample analysis method of claim 8 , wherein solvent vapors are condensed downstream of the thermal desorption tube or the cryo-trap.

12. A sample analysis system, comprising:

an injection port;

a temporally-resolving separator;

a conduit connecting the injection port and the temporally-resolving separator; and

a Fourier transform infrared spectrometer for analyzing time-resolved analytes from the temporally-resolving separator,

wherein,

the injection port is at a temperature sufficiently high to vaporize a solvent and analytes present in a sample; and

the conduit is configured to condense the solvent and maintain the analytes in the vapor phase.

13. The sample analysis system of claim 12 , wherein the temporally-resolving separator is a GC column.

14. The sample analysis system of claim 12 , further comprising an arrangement for cooling or heating or both cooling and heating the conduit and/or heating the injection port.

15. The sample analysis system of claim 12 , further comprising an arrangement for removing the condensed solvent from an interior of the conduit.

16. The sample analysis system of claim 12 , wherein the conduit includes one or more changes in cross section.

17. The sample analysis system of claim 12 , further comprising a controller.

18. The sample analysis system of claim 12 , further comprising an arrangement for detecting a temperature of the conduit or for detecting a temperature of the injection port or for detecting a temperature of both the conduit and the injection port.

19. The sample analysis system of claim 12 , wherein the conduit is configured to condense solvent vapors on inner conduit surfaces.

20. A sample analysis system, comprising:

a thermal desorption tube or a cryo-trap;

a conduit for passing vapors from the thermal desorption tube or the cryotrap to a temporally-resolving separator,

wherein,

the conduit is configured to condense the solvent and maintain the analytes in the vapor phase.

21. The sample analysis system of claim 20 , wherein the system does not employ a secondary thermal desorption tube.

22. The sample analysis system of claim 20 , further comprising a mass spectrometry or an optical spectrometry analyzer.

23. The sample analysis method of claim 8 , wherein the sample is not introduced via an injection port.

24. The sample analysis system of claim 20 , wherein the system does not include an injection port.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 16, 2021
From: MCPARTLAND, KELLY RENEE; SPARTZ, MARTIN L.
To: MLS ACQ, INC. D/B/A MAX ANALYTICAL TECHNOLOGIES
Reel/Frame 058406/0625 →
Continuity (4)
Continuation 16115732 · Aug 29, 2018
Provisional Application 62554350 · Sep 5, 2017
Provisional Application 62551590 · Aug 29, 2017
Related Publication 20220082538A1 · Mar 17, 2022