High accuracy absorbance spectrophotometers

• US 10,151,633 B2
• Filed: 02/09/2017
• Issued: 12/11/2018
• Est. Priority Date: 02/09/2017
• Status: Active Grant

• Current Assignee: Battelle Savannah River Alliance LLC
• Original Assignee: Savannah River Nuclear Solutions LLS
• Inventors: O'Rourke, Patrick E., Lascola, Robert J., Immel, David, Kyser, III, Edward A., Plummer, Jean R.
• Primary Examiner(s): Bologna, Dominic J
• Application Number:
  US15/428,639
• Publication Number:
  US 20180224334A1
• Time in Patent Office: 670 Days
• CPC Class Codes: G01J 2003/102 Plural sources
• CPC Class Codes: G01J 2003/284 Spectral construction
• CPC Class Codes: G01J 2003/2866 Markers; Calibrating of scan
• CPC Class Codes: G01J 3/0297 Constructional arrangements for removing other types of optical noise or for performing calibration
• CPC Class Codes: G01J 3/10 Arrangements of light sources specially adapted for spectrometry or colorimetry
• CPC Class Codes: G01J 3/28 Investigating the spectrum using colour filters G01J3/51
• CPC Class Codes: G01J 3/42 Absorption spectrometry; Double beam spectrometry; Flicker spectrometry; Reflection spectrometry beam switching arrangements G01J3/08
• CPC Class Codes: G01J 3/427 Dual wavelengths spectrometry
• CPC Class Codes: G01N 21/274 Calibration, base line adjustment, drift correction
• CPC Class Codes: G01N 21/31 Investigating relative effect of material at wavelengths characteristic of specific elements or molecules, e.g. atomic absorption spectrometry G01N21/72 takes precedence
• CPC Class Codes: G01N 21/3103 Atomic absorption analysis
• CPC Class Codes: G01N 21/55 Specular reflectivity
• CPC Class Codes: G01N 21/64 Fluorescence; Phosphorescence
• CPC Class Codes: G01N 21/65 Raman scattering

Abstract

Spectrophotometers and spectroscopy processes are described that can provide for in-line calibration at every spectral acquisition as well as for continuous response correction during sample processing. The spectrophotometers include multiple polychromatic light sources that include characteristic emission spectra for use as an internal wavelength drift calibration system that is independent of environmental factors. Correction functions provided by the internal calibration process can be applied continuously and across an entire sample spectrum. The intensity response of each spectrometer in a spectrophotometer can also be monitored and continuously corrected for stray light, dark current, readout noise, etc.

Claims

1. A spectrophotometer comprising:

a first light source configured to emit a first emission spectrum that spans a first wavelength range, the first emission spectrum comprising a plurality of characteristic atomic emissions;

a second light source configured to emit a second emission spectrum that spans a second wavelength range;

a beam splitter configured to combine light emitted from the first light source with light emitted from the second light source and split the combined light to form a sample beam and a reference beam;

a sample cell downstream of and in optical communication with the beam splitter;

a sample spectrometer downstream of and in optical communication with the sample cell;

a reference spectrometer downstream of and in optical communication with the beam splitter; and

a processor in communication with the sample spectrometer and the reference spectrometer, the processor being configured to map the characteristic atomic emissions of the first light source to a first set of responses of the sample spectrometer and to a second set of responses of the reference spectrometer, the processor being further configured to compare and interpolate the first set of responses with the second set of responses and to thereby obtain a correction function, the processor being further configured to apply the correction function to raw sample data communicated to the processor from the sample spectrometer and the reference spectrometer.

2. The spectrophotometer of claim 1, wherein the first light source comprises a xenon lamp.

3. The spectrophotometer of claim 1, wherein the second light source comprises a tungsten-halogen lamp.

4. The spectrophotometer of claim 1, the sample spectrometer comprising a diode array, the first set of responses comprising photoelectric responses of diodes of the diode array.

5. The spectrophotometer of claim 1, the reference spectrometer comprising a diode array, the second set of responses comprising photoelectric responses of diodes of the diode array.

6. The spectrophotometer of claim 1, further comprising light source balancers upstream of and in optical communication with the beam splitter.

7. The spectrophotometer of claim 1, wherein the beam splitter comprises a window that is half reflective and half transmissive to the combined light.

8. The spectrophotometer of claim 1, further comprising a check filter slot.

9. The spectrophotometer of claim 1, further comprising a light attenuator downstream of the beam splitter and in optical communication with the reference spectrometer.

10. The spectrophotometer of claim 1, further comprising one or ore external standards.

11. A method for determining an absorbance spectrum, the method comprising:

combining a first emission spectrum of a first light source with a second emission spectrum of a second light source to form a combined spectra, the first emission spectrum comprising a plurality of characteristic atomic emissions;

splitting the combined spectra to form a sample beam and a reference beam;

directing the sample beam through a sample cell and to a sample spectrometer, the sample spectrometer developing a first data set in response to the sample beam;

directing the reference beam to a reference spectrometer, the reference spectrometer developing a second data set in response to the reference beam;

communicating the first and second data sets to a processor, the processor mapping the characteristic atomic emissions of the first light source to the first data set and to the second data set, the processor further comparing and interpolating the results of the mapping and thereby obtaining a correction function.

12. The method of claim 11, further comprising placing a sample in the sample cell and directing a second sample beam through the sample cell including the sample and to the sample spectrometer, the sample spectrometer developing a third data set in response to the second sample beam, the method further comprising communicating the third data set to the processor, the processor applying the correction function to the third data set and obtaining an absorbance spectrum for the sample.

13. The method of claim 12, further comprising subtracting a blank spectrum from the corrected third data set.

14. The method of claim 12, further comprising correcting the third data set for at least one of dark current and stray light.

15. The method of claim 11, wherein the plurality of characteristic atomic emissions comprise characteristic xenon emissions.

16. The method of claim 11, further comprising attenuating the reference beam.

17. The method of claim 11, wherein the step of mapping the characteristic atomic emissions of the first light source to the first data set and to the second data set comprises binning the first data set and the second data set into multi-point response windows and subjecting the multi-point response windows to spline interpolations.

18. The method of claim 17, wherein the multi-point response windows include a 5-point response window.

19. The method of claim 11, wherein the mapping results in development of 10 or more calibration signals from each of the first data set and the second data set.

20. The method of claim 11, wherein the correction function is a third order polynomial.