Method for determining parameters of a gas-selective electrode

• US 7,799,202 B2
• Filed: 08/02/2005
• Issued: 09/21/2010
• Est. Priority Date: 08/03/2004
• Status: Active Grant

• Current Assignee: Hach Lange GmbH (Danaher Corporation)
• Original Assignee: Hach Lange GmbH (Danaher Corporation)
• Inventors: Bittner, Klaus, Stellmach-Hanulok, Aurelia, Kussmann, Michael, Hahn, Markus, Golitz, Andreas, Battefeld, Manfred
• Primary Examiner(s): Olsen; Kaj K
• Application Number:
  US11/195,010
• Publication Number:
  US 20060027464A1
• Time in Patent Office: 1,876 Days
• Field of Search: 204/416, 204/417, 204/431, 204/432, 205/775, 205/780.5, 700/2, 702/22, 702/23, 73/10.6
• US Class Current: 205/780.5
• CPC Class Codes: G01N 27/4163 checking the operation of, or calibrating, the measuring apparatus G01N27/3274, G01N27/4175 and G01N33/0006 take precedence

Abstract

Gas-selective electrodes in liquid analyzing devices have a characteristic curve K with a linear portion L and a non-linear portion NL. In the non-linear portion NL, the characteristic previously could only be estimated so that determinations of the concentration were rather inexact. According to the present application, the electrode is rinsed with an acid and the zero point voltage U_N at the electrode is determined during the rinsing. Using the zero point voltage U_N, the non-linear portion NL of the characteristic K is determined with high precision so that even low concentrations c can be determined with great accuracy.

Claims

1. A method for determining parameters of a characteristic curve of a gas-selective electrode in an automatic liquid analyzing device, the method comprising the following steps:

rinsing the electrode with an acid, and

determining a zero point voltage U_N present at the electrode during the acid rinsing, wherein a depletion signal is output when the zero point voltage U_N reaches a predetermined depletion value.

2. The method of claim 1, wherein the acid rinsing is performed during an automatic cleaning of the electrode.

3. The method of claim 1, wherein the electrode is an ammonia electrode.

4. The method of claim 1, wherein the rinsing acid is citric acid.

5. The method of claim 1, further including:

determining a non-linear portion NL of the characteristic curve K of the electrode by interpolating the characteristic curve K between a linear portion L and the zero point voltage U_N according to an exponential function.

6. The method of claim 5, wherein the exponential interpolation function is:

U=U_N(1−

e<sup>(E/UN(log c−

F))</sup>)

where

U is an output electrode voltage,

U_N is the zero point voltage of the electrode,

E is a constant quantifying the curvature of the exponential function,

c is a concentration of the measuring gas,

the linear and the non-linear portions L, NL of the characteristic curve K transition at a limit point G,

c_G is a limit concentration at the limit point G,

F is a position of the exponential function on a concentration axis,

the transition at the limit point G is differentiable, and

at least one of the limit point concentration c_G and the constant of curvature E is fixed.

7. The method of claim 6, wherein the constant of curvature E is fixed.

8. An apparatus for performing the method of claim 1.

9. An automatic liquid sample analysis device comprising:

a gas-selective electrode;

a means for rinsing the electrode with an acid;

a control processor for determining a characteristic curve K of the gas-selective electrode, the control processor being programmed to;

determine a zero point voltage U_N present at the gas-selective electrode during an acid rinse; and

output a depletion signal in response to the zero point voltage U_N reaching a predetermined depletion value.

10. The apparatus of claim 9 wherein the processor is further programmed to:

determine a non-linear portion NL of the characteristic curve K between a linear portion L and the zero point voltage U_N by interpolating with the interpolation function;

U=U_N(1−

e<sup>(E/UN(log c−

F))</sup>)

where

U is an output electrode voltage, U_N is the zero point voltage of the gas-selective electrode,

E is a electrode specific constant of curvature of the exponential function,

c is a concentration of the measuring gas,

the linear and the non-linear portions L, NL of the characteristic curve K transition at a limit point G,

c_G is a limit concentration at the limit point G,

F is a position of the exponential function on a concentration axis,

a transition at the limit point G is differentiable, and

at least one of the limit point concentration c_G and the constant of curvature E is fixed.

11. The apparatus of claim 9 wherein the processor is further programmed to:

determine a concentration from an output of the gas-selective electrode after the acid rinsing and during sampling of a sample using the determined concentration curve K.