Total organic carbon analysis
The present invention provides an apparatus and method for measuring carbon (any one or all of TC, TOC, or TIC) in a sample matrix. In an embodiment, a method for measuring carbon in a sample composition is provided. The method comprises providing an apparatus comprising a reaction chamber and a diamond coated electrode, wherein the diamond coated electrode is doped with boron. The apparatus further comprises a detector. In addition, the method comprises contacting the sample composition with the electrode. The method further comprises applying an alternating current to the electrode at a sufficient voltage to produce carbon dioxide. Moreover, the method comprises measuring the amount of carbon dioxide produced.
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1. Field of the Invention
This invention relates generally to the field of measuring carbon in a sample composition. More particularly, this invention relates to measuring carbon as Total Organic Carbon (TOC), Total Inorganic Carbon (TIC) or Total Carbon (TC) using electrochemical oxidation.
2. Background of the Invention
The need to measure carbon in aqueous samples exists in matrixes from ultra-pure water to waste water and industrial solutions for a variety of reasons. Historically, the analysis equipment to accurately measure carbon in an aqueous solution involved large equipment and hazardous reagents, such as strong acid and oxidizing agents. The use of electrochemical oxidation of carbon may eliminate at least one of these reagents and, when combined with a detection technique to quantify the resultant carbon dioxide gas (e.g., in solution, measured in a headspace or purged from the sample and transported with carrier gas to a detector), promises a versatile, easy to use, and cost-effective alternative for accurately determining TOC levels in a solution. Thus, the development of a safe and cost-effective electrochemical device capable of oxidizing organic carbon and allowing determination of TOC in a sample composition would represent a significant advance in the art.
Electrodes are used in the typical electrochemical cell for oxidation of carbon. The most common working electrode material has typically been carbon-based or made from metals such as platinum, silver, gold, mercury, or nickel. Drawbacks to such electrodes include poor oxidation. Further drawbacks include the self-consuming nature (e.g., reduction/oxidation) of the electrodes themselves. To overcome these limitations, conductive diamond film electrodes have been developed. Diamond film electrodes include a substrate material coated with diamond or diamond-like film wherein the diamond coated electrodes are doped to provide conductivity (e.g., boron doped). Drawbacks to the conventional diamond or diamond-like film electrodes include the tendency of electrodes to fail due to contamination and corrosion. Additional drawbacks include insufficient oxidation. Consequently, there still remains a need for a method and apparatus for measuring carbon using electrochemical oxidation with reduced electrode contamination and corrosion.
BRIEF SUMMARYThese and other needs in the art are addressed in one embodiment by an apparatus for measuring the carbon concentration of a sample. The apparatus comprises a reaction chamber and a detection system, whereby varying control algorithms allows for the determination of carbon as Total Organic Carbon (TOC), Total Inorganic Carbon (TIC) or Total Carbon (TC). In addition, the apparatus comprises a set of diamond coated electrodes, wherein the diamond coated electrodes may be doped to provide conductivity (e.g., doped with boron).
In another embodiment, these and other needs in the art are addressed by a method for measuring carbon in a sample composition. The method comprises providing an apparatus comprising a reaction chamber with a set of diamond coated electrodes, wherein the diamond coated electrodes may be doped with boron. The apparatus further comprises a detection system to determine CO2 concentrations in the gas phase, liquid phase or a combination of the two. In addition, the method comprises contacting the sample composition with the electrode. The method further comprises applying a sufficiently controlled voltage to the electrode to produce carbon dioxide. Moreover, the method comprises measuring the amount of carbon dioxide produced.
The foregoing has outlined rather broadly the features and technical advantages of the present invention in order that the detailed description of the invention that follows may be better understood. Additional features and advantages of the invention will be described hereinafter that form the subject of the claims of the invention. It should be appreciated by those skilled in the art that the conception and the specific embodiments disclosed may be readily utilized as a basis for modifying or designing other structures for carrying out the same purposes of the present invention. It should also be realized by those skilled in the art that such equivalent constructions do not depart from the spirit and scope of the invention as set forth in the appended claims.
BRIEF DESCRIPTION OF THE DRAWINGSFor a detailed description of the preferred embodiments of the invention, reference will now be made to the accompanying drawings in which:
The following description details a method and an apparatus for measuring carbon in an aqueous sample composition. Without being limited by theory, the method and apparatus are capable of measuring carbon with minimum contamination to the electrodes resulting in longer effective use and superior cost efficiency. Two electrodes provide the oxidation capability. The control system for these electrodes may optimize the self-cleaning nature of the electrodes. The apparatus may be configured to process discrete samples or for continuous sampling using appropriate electrode geometries. The geometries include but are not limited to batch or flow through designs. The geometries may include fixed or variable gap electrodes of any design that allows the electrodes electrical isolation.
In an embodiment as shown in
In an embodiment, the diamond coated substrates of inner and outer elements 205, 210 are doped with a doping material. Without limitation, examples of suitable doping materials include boron, zinc, nitrogen, phosphorous, and sulfur. In an embodiment, the doping material is boron. The diamond coated substrates may be doped by any suitable method such as during chemical vapor deposition.
As further illustrated in
It is to be further understood that the configuration of electrode 102 is not limited to the configuration illustrated in
As shown in
As shown in
As further shown in
As shown in
In an alternative embodiment, the carbon dioxide may be dried in a drier to remove moisture prior to being measured by detector 106. Without limitation, examples of suitable driers include a dryer permeation tube or an anhydrous tube. In another alternative embodiment, the carbon dioxide may be passed through a scrubber to remove acid vapors from the carbon dioxide. In further embodiments, the carbon dioxide may be directed into a trap, from which it is released into detector 106. Any suitable trap may be used that may retain carbon dioxide until a suitable amount of carbon dioxide is accumulated prior to release to detector 106.
As further shown in
In an embodiment as illustrated in
Although the present invention and its advantages have been described in detail, it should be understood that various changes, substitutions and alterations may be made herein without departing from the spirit and scope of the invention as defined by the appended claims.
Claims
1. An apparatus for measuring carbon in a sample composition, comprising:
- a reaction chamber;
- a diamond coated electrode, wherein the diamond coated electrode is doped with a doping material;
- and a detector.
2. The apparatus of claim 1, further comprising two electrodes.
3. The apparatus of claim 1, wherein the electrode comprises an inner element and an outer element.
4. The apparatus of claim 3, wherein the inner element comprises a rod, and the outer element comprises a tube.
5. The apparatus of claim 3, wherein the inner element comprises a mesh tube, and wherein the outer element comprises a mesh tube.
6. The apparatus of claim 3, wherein the electrode comprises an insulator disposed between the inner element and the outer element.
7. The apparatus of claim 1, wherein the doping material is boron.
8. The apparatus of claim 1, wherein the detector comprises a gas phase detector.
9. The apparatus of claim 1, wherein the apparatus further comprises a gas diffusion membrane and a collection chamber.
10. The apparatus of claim 9, wherein the gas diffusion membrane allows carbon dioxide to diffuse from the reaction chamber to the collection chamber.
11. The apparatus of claim 9, wherein the detector is disposed in the collection chamber.
12. The apparatus of claim 1, wherein the apparatus further comprises a carbon dioxide trap.
13. The apparatus of claim 1, wherein an alternating current voltage is applied to the electrode.
14. The apparatus of claim 13, wherein the alternating current voltage is applied at a frequency between about 1 Hz and about 100 Hz.
15. The apparatus of claim 13, wherein the alternating current voltage is applied from about 5 volts to about 300 volts.
16. A method for measuring carbon in a sample composition, comprising:
- (A) providing an apparatus comprising: a reaction chamber; a diamond coated electrode, wherein the diamond coated electrode is doped with a doping material; and a detector;
- (B) contacting the sample composition with the electrode;
- (C) applying an alternating current to the electrode at a sufficient voltage to produce carbon dioxide; and
- (D) measuring the amount of carbon dioxide produced.
17. The method of claim 16, wherein the apparatus comprises two electrodes.
18. The method of claim 16, wherein the electrode comprises an inner element and an outer element.
19. The method of claim 18, wherein the inner element comprises a rod, and the outer element comprises a tube.
20. The method of claim 18, wherein the inner element comprises a mesh tube, and wherein the outer element comprises a mesh tube.
21. The method of claim 18, wherein the electrode comprises an insulator disposed between the inner element and the outer element.
22. The method of claim 16, wherein the doping material is boron.
23. The method of claim 16, further comprising feeding a carrier gas to the reaction chamber at a sufficient rate to transport the carbon dioxide to the detector.
24. The method of claim 16, wherein step (C) further comprises diffusing the carbon dioxide through a gas diffusion membrane to a collection chamber.
25. The method of claim 24, further comprising feeding a carrier gas to the collection chamber at a sufficient rate to transport the carbon dioxide to the detector.
26. The method of claim 24, wherein the detector is disposed in the collection chamber.
27. The method of claim 16, further comprising trapping the carbon dioxide prior to measuring the amount of carbon dioxide.
28. The method of claim 16, wherein step (D) further comprises measuring the amount of carbon dioxide with a liquid phase detector.
Type: Application
Filed: Feb 9, 2006
Publication Date: Aug 9, 2007
Applicants: OI Analytical (College Station, TX), O I Corporation (College Station, TX)
Inventors: Gary Erickson (College Station, TX), Karl Williams (Bryan, TX)
Application Number: 11/350,420
International Classification: G01N 33/00 (20060101);