Device and method for cavity detected high-speed diffusion chromatography
A chromatography sensor device is provided that includes a first loading chamber into which a sample fluid can be inserted, a second loading chamber into which a buffer fluid can be inserted, a diffusion column adapted to communicate with the first loading chamber and the second loading chamber and having walls lined with a chromatography stationary phase, a first high finesse optical cavity communicating with the diffusion column at a first distance from the gate, a second high finesse optical cavity communicating with the diffusion column at a second distance from the gate; and one or more lasers for generating laser frequencies for exciting the first and second high finesse optical cavities, whereby the sample fluid may diffuse into the diffusion column containing the buffer fluid and the one or more lasers and associated detectors may be used to detect a molecule of interest in the sample fluid.
1. A chromatography sensor device comprising:
a loading chamber configured to receive a sample fluid;
a diffusion column configured to communicate with the loading chamber, wherein the diffusion column has walls lined with a chromatography stationary phase material, and wherein the chromatography stationary phase material lining the walls defines a pathway through the diffusion column that is configured to contain a buffer fluid;
a gate that divides the diffusion column from the loading chamber, wherein the gate is configured to be opened to allow the sample fluid in the loading chamber to diffuse through the diffusion column without being transported by a mobile phase; and
one or more analyte detection devices located at fixed distances from the gate, said analyte detection devices being configured to detect an analyte in sample fluid as it diffuses through the diffusion column.
2. The device of claim 1 , wherein the buffer fluid is a gas and the sample fluid is a gas.
3. The device of claim 1 , wherein the buffer fluid is a liquid and the sample fluid is a liquid.
4. The device of claim 1 , further comprising an estimator that receives signals from the detection devices and provides estimated concentrations of different analyte species present in the sample fluid.
5. The device of claim 1 , wherein the diffusion column is formed from two removable plates supported in a monolithic spacer.
6. The device of claim 1 , further including one or more additional diffusion columns configured to communicate with the loading chamber, wherein each diffusion column of the device has walls that are lined with a different chromatography stationary phase material.
7. A method for estimating the concentration of different molecules present in a sample fluid, the method comprising the steps of:
providing a chromatography sensor device according to claim 1 ;
introducing a sample fluid into the loading chamber of the chromatography sensor device;
opening the gate that divides the diffusion column from the loading chamber;
allowing the sample fluid to diffuse along the diffusion column lined with the chromatography stationary phase and containing the buffer fluid without entraining the sample fluid in a mobile phase; and
detecting analytes present in the sample fluid using detectors provided at two or more fixed distances from the gate.
8. The method of claim 7 , wherein the buffer fluid is a gas and the sample fluid is a gas.
9. The method of claim 7 , wherein the buffer fluid is a liquid and the sample fluid is a liquid.
10. The method of claim 7 , wherein the loading chamber and the diffusion column are operated at pre-determined fixed temperatures.
11. The method of claim 7 , wherein the loading chamber and diffusion column are operated at programmed time-varying temperatures.
12. The method of claim 7 , wherein the step of detecting comprises:
exciting first and second optical cavities communicating with the diffusion column with light from one or more lasers; and
detecting optical absorption losses at laser wavelengths in the optical cavities using the detectors.
13. The method of claim 12 wherein the detection step further comprises:
estimating a concentration of different molecules present in the sample fluid based on detected absorption losses as a function of time.
14. A chromatography sensor device comprising:
a loading chamber configured to receive a sample fluid;
a diffusion column configured to communicate with the loading chamber, wherein the diffusion column has walls lined with a chromatography stationary phase material, and wherein the chromatography stationary phase material lining the walls defines a pathway through the diffusion column that is configured to contain a buffer fluid;
a gate that divides the diffusion column from the loading chamber, wherein the gate is configured to be opened to allow the sample fluid in the loading chamber to diffuse through the diffusion column without being transported by a mobile phase;
a first optical cavity communicating with the diffusion column at a first distance from the gate;
a second optical cavity communicating with the diffusion column at a second distance from the gate; and
detection devices associated with each optical cavity, said detection devices being configured to detect an analyte in sample fluid as it diffuses through the diffusion column.
15. The device of claim 14 , further comprising a second loading chamber configured to receive a buffer fluid, and wherein the diffusion column is configured to communicate with the second loading chamber.
16. The device of claim 14 , wherein the buffer fluid is a gas and the sample fluid is a gas.
17. The device of claim 14 , wherein the buffer fluid is a liquid and the sample fluid is a liquid.
18. The device of claim 14 , further comprising a plurality of mirrors associated with each optical cavity and a removable mirror cap associated with each optical cavity which is removable to allow for replacement of said plurality of mirrors.
19. The device of claim 18 , further comprising a PZT actuator associated with each optical cavity that moves at least one mirror in order to adjust an optical cavity mode.
20. A chromatography sensor device comprising:
a loading chamber configured to receive a sample fluid;
a diffusion column configured to communicate with the loading chamber, wherein the diffusion column has walls lined with a chromatography stationary phase material, and wherein the chromatography stationary phase material lining the walls defines a pathway through the diffusion column that is configured to contain a buffer fluid;
a gate that divides the diffusion column from the loading chamber, wherein the gate is configured to be opened to allow the sample fluid in the loading chamber to diffuse through the diffusion column without being transported by a mobile phase;
a first optical cavity communicating with the diffusion column at a first distance from the gate;
a second optical cavity communicating with the diffusion column at a second distance from the gate;
one or more lasers for generating laser frequencies for exciting the first and second optical cavities; and
detection devices associated with each optical cavity, said detection devices being configured to detect an analyte in sample fluid as it diffuses through the diffusion column.
21. The device of claim 20 , wherein the buffer fluid is a gas and the sample is a gas.
22. The device of claim 20 , wherein the buffer fluid is a liquid and the sample fluid is a liquid.
23. The device of claim 20 , wherein only one laser is used within the device, and the device further includes an optical frequency comb in optical communication with each cavity.
24. The device of claim 20 , further comprising optics and electronics for locking frequencies of the lasers to resonant optical frequencies of the optical cavities.
25. The device of claim 20 , wherein the diffusion column is formed from two removable plates supported in a monolithic spacer.
26. The device of claim 20 , wherein the detection devices are configured to detect the absorption losses of the lasers in the optical cavities using either direct cavity transmission (DCT), cavity ring-down spectroscopy (CRDS), noise immune cavity enhanced-optical heterodyne molecular spectroscopy (NICE-OHMS), or integrated cavity output spectroscopy (ICOS).