The three above-identified patent applications are hereby incorporated herein by reference.
This invention relates to methods and apparatus for identifying and characterizing substances in general, and more particularly to methods and apparatus for identifying and characterizing substances using Raman spectroscopy.
Raman spectroscopy is an effective tool for identifying and characterizing a vast array of substances.
In Raman spectroscopy, laser light of a known wavelength (typically infrared or near infrared) is directed at a specimen. The laser light (also sometimes referred to as the Raman pump) interacts with the electron clouds in the molecules of the specimen and, as a result of this interaction, experiences selected wavelength shifting. The precise nature of this wavelength shifting depends upon the materials present in the specimen. A unique wavelength signature (typically called the Raman signature) is produced by each specimen. This unique Raman signature permits the specimen to be identified and characterized. More specifically, the spectrum of light returning from the specimen is analyzed with a spectrometer so as to identify the Raman-induced wavelength shifting in the Raman pump light, and then this wavelength signature is compared (e.g., by a computer) with a library of known Raman signatures, whereby to identify the precise nature of the specimen.
Raman spectroscopy is widely used in scientific, commercial and public safety areas.
Recent technological advances have made it possible to significantly reduce the size and cost of Raman spectroscopy systems. This has in turn increased the range of practical applications for Raman spectroscopy. For example, portable units have recently become available for various field uses, such as the on-site identification of potentially hazardous substances.
In some instances it can be desirable for the Raman spectroscopy system to have its optical probe head (i.e., the light launch and collector portions of the system) separated from the main body of the Raman system (e.g., the laser, spectrometer, computer, etc.). For example, this can be useful in situations where the entire Raman spectroscopy system will not conveniently fit adjacent to the specimen. In this case, the optical probe head is typically connected to the main body of the Raman system by a flexible optical connector.
Additionally, in some instances it can be desirable for the optical probe head to be disposable. For example, where specimen purity is of concern, or where the specimen may be highly toxic, it may be desirable for the optical probe head to be replaced after use.
As noted above, where the Raman spectroscopy system has its optical probe head separated from the main body of the Raman system, the optical probe head is typically connected to the main body of the Raman system by a flexible optical connector. This flexible optical connector generally comprises a long, thin light guide, or guides, to deliver the excitation light to the specimen and to collect the Raman signature from the specimen. It is also generally desirable that the light guide, or guides, be flexible, rugged, and compact.
Conventional optical fibers have traditionally been used as the light guide(s) to deliver the excitation light to the specimen and to collect the Raman signature from the specimen. However, the amorphous nature of the glass used in a conventional optical fiber (and, specifically, the non-linear coefficients of the optical fiber's refractive index), together with the high optical power of the pump laser, typically causes a relatively broadband spurious background noise signal, having a significant intensity, to be generated as the pump light travels through the fiber.
As a result, where a single conventional optical fiber is used to both deliver the pump light to the specimen and to collect the Raman signature from the specimen, the relatively broadband spurious background noise signal from the fiber is superimposed on the Raman signature of the specimen. See
For this reason, one optical fiber (the excitation fiber) is generally used to deliver the excitation light to the specimen, and another optical fiber (the collection fiber) is generally used to collect the Raman signature from the specimen. See
In any case, the complexity of a two fiber and filter construction (i.e., excitation fiber, filter and collection fiber) increases the cost of the optical probe head and makes a disposable optical probe head significantly less feasible.
Accordingly, a primary object of the present invention is to provide an improved Raman spectroscopy system which overcomes the aforementioned shortcomings of currently available systems.
Another object of the present invention is to provide an improved optical probe assembly which is configured so as to avoid generating a significant relatively broadband spurious background noise signal when delivering the pump light to the specimen.
In one preferred embodiment of the present invention, there is provided an improved Raman spectroscopy system which comprises an improved optical probe assembly utilizing a single light guide to both deliver pump light to the specimen and to collect the Raman signature from the specimen, with the single light guide being constructed so as to minimize any relatively broadband spurious background noise signal when delivering pump light to the specimen. As a result, the signal-to-noise ratio of the Raman signature will remain robust even where only a single light guide is used, thereby maintaining sensitivity of the system and enhancing specimen selectivity.
In one preferred form of the invention, the optical probe assembly preferably comprises an optical guide comprising a core region and a surrounding cladding region, wherein the core region is constructed so as to minimize the creation of any relatively broadband spurious background noise signal when passing the pump light, and the cladding region is constructed so as to satisfy wave guiding reflection requirements.
The improved optical probe assembly is preferably disposable due to its simplicity.
In another form of the present invention, there is provided an optical probe assembly for conveying Raman pump light to a specimen and for conveying a Raman signature from the specimen to an optical spectrum analyzer, the optical probe assembly comprising a light guide, wherein the light guide comprises a core region and a surrounding cladding region, wherein the core region is constructed so as to minimize the creation of a relatively broadband spurious background noise signal when conveying the Raman pump light to the specimen, and the cladding region is constructed so as to satisfy the wave guiding reflection requirements of the Raman pump light and the Raman signature.
In another form of the present invention, there is provided a Raman spectroscopy system comprising:
a laser for producing Raman pump light;
an optical probe assembly for conveying the Raman pump light to a specimen and for conveying a Raman signature from the specimen to an optical spectrum analyzer, the optical probe assembly comprising a light guide, wherein the light guide comprises a core region and a surrounding cladding region, wherein the core region is constructed so as to minimize the creation of a relatively broadband spurious background noise signal when conveying the Raman pump light to the specimen, and the cladding region is constructed so as to satisfy wave guiding reflection requirements of the Raman pump light and the Raman signature; and
an optical spectrum analyzer for receiving the Raman signature of a specimen and identifying and characterizing the specimen based upon the spectrum of the Raman signature.
In another form of the present invention, there is provided a method for conducting Raman spectroscopy comprising:
producing Raman pump light;
conveying the Raman pump light through an optical probe assembly to a specimen and conveying a Raman signature from the specimen through the optical probe assembly to an optical spectrum analyzer, the optical probe assembly comprising a light guide, wherein the light guide comprises a core region and a surrounding cladding region, wherein the core region is constructed so as to minimize the creation of a relatively broadband spurious background noise signal when conveying the Raman pump light to the specimen, and the cladding region is constructed so as to satisfy wave guiding reflection requirements of the Raman pump light and the Raman signature; and
identifying and characterizing the specimen based upon the spectrum of the Raman signature.
These and other objects and features of the present invention will be more fully disclosed or rendered obvious by the following detailed description of the preferred embodiments of the invention, which is to be considered together with the accompanying drawings wherein like numbers refer to like parts and further wherein:
Looking first at
Laser 15 may comprise any laser suitable for use in Raman spectroscopy. By way of example but not limitation, laser 15 may comprise one or more >300 mW, 785 nm semiconductor lasers with limited linewidths (e.g., ˜2 cm−1). The output of laser 15 is delivered into the optical probe assembly 20 for delivery to the specimen.
Optical probe assembly 20 generally comprises a light guide 30 for delivering excitation (pump) light to the specimen and for collecting the Raman signature from the specimen, a lens 35 for efficient delivery of light to the specimen and for efficient collection of light from the specimen, and a dichroic beam splitter 38 for directing at least some of the returning light to optical spectrum analyzer 25.
Light guide 30 preferably comprises a core region 40 and a cladding region 45 (
Light guide 30 preferably comprises a liquid-filled structure, e.g., a capillary structure.
In one preferred form of the invention, core region 40 comprises heavy water (D2O). The “low Raman cross-section” of heavy water (D2O) ensures that the high power excitation (pump) light does not generate spurious Raman signals in the region of interest (e.g., near infrared). In other words, by making core region 40 out of heavy water (D2O), the pump light can be delivered from laser 15 to specimen 10 without creating a significant relatively broadband spurious background noise signal. As a result, a single light guide, i.e., the heavy water (D2O) filled light guide 30, can be used to carry both the excitation laser light to specimen 10 and to collect the Raman signature from specimen 10.
Using heavy water (D2O) to form the core region 40 also makes it possible to achieve low loss for both the excitation laser being delivered to specimen 10 and the Raman signature being collected from specimen 10. A plot of the loss spectrum of D2O versus H2O is shown in
Thus, heavy water (D2O) has the dual advantages of generating a minimal relatively broadband spurious background noise signal, and relatively little optical loss, in the wavelength range of interest (e.g., 780 nm to 1100 nm). Other solvents generally produce a substantial relatively broadband spurious background noise signal, and/or exhibit relatively high optical loss, in the wavelength range of interest (e.g., 780 nm to 1100 nm). However, the present invention is intended to encompass core regions formed out of liquids in addition to heavy water (D2O) which are capable of generating a minimal relatively broadband spurious background noise signal, and relatively little optical loss, in the wavelength range of interest.
As noted above, cladding region 45 is constructed so as to satisfy wave guiding reflection requirements. Where core region 40 comprises heavy water (D2O), which has an optical index of ˜1.32, cladding region 45 has a cladding index of less than 1.32. Cladding region 45 may be made from a plastic material (e.g., Dupont TeflonAF or other appropriate polymers), etc.
Light guide 30 may also comprise a photonic crystal structure, with cladding region 45 comprising engineered photonic bandgap (crystal) structures.
After the return light is received by light guide 30, some of the returning light is directed through dichroic beam splitter 38 and into optical spectrum analyzer 25. The dichroic beam splitter 38 is used to spatially separate the reflected pump signal from the specimen's Raman signature.
Thus, novel light guide 30 allows the co-propagation of the high intensity laser (pump) light with the Stokes-shifted Raman signature from the specimen, while introducing a minimal relatively broadband spurious background noise signal onto the collected signature. The light can be either multi-mode (e.g., with a core size of ˜100-200 μm and a numerical aperture of >0.3), or single-mode, depending on the spatial mode properties of the laser used.
Light guide 30 can include a ruggedized external sheath 50 for environmental protection.
It is to be understood that the present invention is by no means limited to the particular constructions herein disclosed and/or shown in the drawings, but also comprises any modifications or equivalents within the scope of the invention.
This patent application: (i) is a continuation-in-part of prior U.S. patent application Ser. No. 10/826,706, filed Apr. 16, 2004 now U.S. Pat. No. 7,110,109 by Kevin J. Knopp et al. for RAMAN SPECTROSCOPY SYSTEM AND METHOD AND SPECIMEN HOLDER THEREFOR; (ii) is a continuation-in-part of pending prior U.S. patent application Ser. No. 11/117,940, filed Apr. 29, 2005 by Peidong Wang et al. for METHOD AND APPARATUS FOR CONDUCTING RAMAN SPECTROSCOPY; and (iii) claims benefit of prior U.S. Provisional Patent Application Ser. No. 60/698,270, filed Jul. 11, 2005 by Kevin J. Knopp et al. for DISPOSABLE OPTICAL PROBE FOR RAMAN SPECTROSCOPY.
Number | Name | Date | Kind |
---|---|---|---|
3017513 | Messelt | Jan 1962 | A |
3906241 | Thompson | Sep 1975 | A |
4045119 | Eastgate | Aug 1977 | A |
5026160 | Dorain et al. | Jun 1991 | A |
5048959 | Morris et al. | Sep 1991 | A |
5483337 | Barnard et al. | Jan 1996 | A |
5651018 | Mehuys et al. | Jul 1997 | A |
5675689 | Nath | Oct 1997 | A |
5734165 | Unal et al. | Mar 1998 | A |
5828450 | Dou et al. | Oct 1998 | A |
6069689 | Zeng et al. | May 2000 | A |
6249349 | Lauer | Jun 2001 | B1 |
6303934 | Daly et al. | Oct 2001 | B1 |
6608677 | Ray et al. | Aug 2003 | B1 |
6803328 | McCullough | Oct 2004 | B2 |
6862092 | Ibsen et al. | Mar 2005 | B1 |
6977723 | Lemmo et al. | Dec 2005 | B2 |
20020033944 | Sharts et al. | Mar 2002 | A1 |
20030002548 | Boscha | Jan 2003 | A1 |
20030002839 | Clow et al. | Jan 2003 | A1 |
20030085348 | Megerle | May 2003 | A1 |
20030197860 | Rice | Oct 2003 | A1 |
20040039274 | Benaron et al. | Feb 2004 | A1 |
20040109230 | Matsushita et al. | Jun 2004 | A1 |
20040165183 | Marquardt et al. | Aug 2004 | A1 |
20040165254 | Tokura et al. | Aug 2004 | A1 |
20040252299 | Lemmo et al. | Dec 2004 | A9 |
20040263843 | Knopp et al. | Dec 2004 | A1 |
20050083521 | Kamerman | Apr 2005 | A1 |
20060023209 | Lee et al. | Feb 2006 | A1 |
20060170917 | Vakhshoori et al. | Aug 2006 | A1 |
Number | Date | Country |
---|---|---|
WO 02101365 | Dec 2002 | WO |
Number | Date | Country | |
---|---|---|---|
20070024848 A1 | Feb 2007 | US |
Number | Date | Country | |
---|---|---|---|
60698270 | Jul 2005 | US |
Number | Date | Country | |
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Parent | 10826706 | Apr 2004 | US |
Child | 11484534 | US | |
Parent | 11117940 | Apr 2005 | US |
Child | 10826706 | US |