Rugged dissolved carbon dioxide monitor for high purity water

• US 4,801,551 A
• Filed: 10/06/1986
• Issued: 01/31/1989
• Est. Priority Date: 10/06/1986
• Status: Expired due to Fees

• Current Assignee: Westinghouse Electric Corporation (Paramount Global (f/k/a ViacomCBS Inc.))
• Original Assignee: Westinghouse Electric Corporation (Paramount Global (f/k/a ViacomCBS Inc.))
• Inventors: Carlson, Gerald L., Bellows, James C., Byers, William A.
• Primary Examiner(s): Marcus, Michael S.
• Assistant Examiner(s): McMahon, Timothy M.
• Application Number:
  US06/915,605
• Time in Patent Office: 848 Days
• Field of Search: 436/133, 436/150, 436/68
• US Class Current: 436/133
• CPC Class Codes: G01N 27/06 of a liquid involving electrolysis G01N27/26
• CPC Class Codes: G01N 33/18 Water
• CPC Class Codes: G01N 33/1813 Specific cations in water, e.g. heavy metals
• CPC Class Codes: Y10T 436/204998 Inorganic carbon compounds

Abstract

A continuous on-line monitor of carbon dioxide dissolved in high purity water includes a cation conductivity cell and associated bridge for measuring first and second cation conductivities at first and second temperature and a heater for heating the sample from the first to the second temperature. A microcomputer calculates first and second concentrations of a fully dissociated acid alone and carbon dioxide alone, respectively, which will produce the first measured cation conductivity at the first temperature and then determines the actual carbon dioxide concentration from the first and second concentrations and the second measured cation conductivity.

Claims

1. A method of determining dissolved carbon dioxide concentration in a sample, comprising the steps of:

(a) measuring a first cation conductivity in the sample at a first temperature;

(b) measuring a second cation conductivity in the sample at a second temperature different from the first temperature; and

(c) determining an actual concentration of carbon dioxide in the sample in dependence upon the first and second measured cation conductivities.

2. A method as recited in claim 1, wherein step (c) comprises the steps of:

(ci) determining a first concentration of a fully dissociated acid which will produce the first measured cation conductivity at the first temperature;

(cii) determining a second concentration of carbon dioxide which will produce the first measured cation conductivity at the first temperature; and

(ciii) determining the actual concentration of carbon dioxide in dependence upon the first and second concentrations and the second measured cation conductivity.

3. A method as recited in claim 2, wherein the fully dissociated acid is one of hydrogen sulfate and hydrogen chloride.

4. A method as recited in claim 2,

wherein step (ciii) comprises the steps of:

(ciii1) determining a first predicted cation conductivity of the first concentration of tne fully dissociated acid alone at the second temperature;

(ciii2) determining a second predicted cation conductivity of the second concentration of carbon dioxide alone at the second temperature;

(ciii3) calculating a first difference between the first predicted and second measured cation conductivities;

(ciii4) calculating a second difference between the first and second predicted cation conductivities;

(ciii5) calculating a ratio factor by dividing the first difference by the second difference; and

(ciii6) calculating the actual concentration of carbon dioxide by multiplying the second concentration of carbon dioxide by the ratio factor.

5. A method as recited in claim 4, wherein the fully dissociated acid is one of hydrogen sulfate and hydrogen chloride.

6. A method as recited in claim 2,

wherein step (ciii) comprises the steps of:

(ciii1) determining a first predicted cation conductivity of the first concentration of the fully dissociated acid at the second temperature;

(ciii2) determining a second predicted cation conductivity of the second concentration of carbon dioxide alone at the second temperature;

(ciii3) determining a first slope of a first line connecting first and second points representing the first measured and first predicted cation conductivities, respectively, plotted versus temperature;

(ciii4) determining a second slope of a second line connecting the first point and a third point representing the second predicted cation conductivity, plotted versus temperature;

(ciii5) determining a third slope of a third line connecting the first point and a fourth point representing the second measured cation conductivity, plotted versus temperature; and

(ciii6) determining the actual concentration of carbon dioxide from the first, second and third slopes.

7. A method as recited in claim 6, wherein the fully dissociated acid is one of hydrogen sulfate and hydrogen chloride.

8. A method as recited in claim 6,

wherein step (ciii6) comprises the steps of:

(ciii6A) determining a fourth slope of a fourth line connecting fourth and fifth points representing the first and second slopes, respectively, plotted versus carbon dioxide concentration, where the fourth point has zero carbon dioxide concentration; and

(ciii6B) determining the actual concentration of carbon dioxide which corresponds to an X-coordinate of a sixth point on the fourth line, the third slope corresponding to a Y-coordinate of the sixth point.

9. A method as recited in claim 8, wherein the fully dissociated acid is one of hydrogen sulfate and hydrogen chloride.

10. A methodf for determining carbon dioxide concentration in a sample of water used for electrical power generation, comprising the steps of:

(a) measuring a first cation conductivity of the sample at a first temperature;

(b) determining a first concentration of sulfate which alone will produce the first measured cation conductivity at the first temperature;

(c) determining a second concentration of carbon dioxide which alone will produce the first measured cation conductivity at the first temperature;

(d) heating the sample to a second temperature different from the first temperature;

(e) measuring a second cation conductivity of the sample at the second temperature;

(f) determining first and second predicted cation conductivities of the first and second concentrations of sulfate alone and carbon dioxide alone, respectively, at the second temperature; and

(g) determining the actual carbon dioxide concentration in dependence upon the second concentration of carbon dioxide and differences between the second measured and first and second predicted cation conductivities.