Method for calibration of a pH measuring element

• US 5,658,451 A
• Filed: 11/28/1995
• Issued: 08/19/1997
• Est. Priority Date: 02/01/1995
• Status: Expired due to Term

• Current Assignee: Avl Medical Instruments AG (Roche Holding AG)
• Original Assignee: Avl Medical Instruments AG (Roche Holding AG)
• Inventors: Leiner, Marco Jean-Pierre
• Primary Examiner(s): TUNG, TA HSUNG
• Application Number:
  US08/563,277
• Time in Patent Office: 630 Days
• Field of Search: 204/400, 204/401, 204/403, 204/416, 204/418, 204/419, 204/420, 205/775, 205/787.5, 205/792, 436/8, 436/9, 436/11, 436/19
• US Class Current: 205/787.5
• CPC Class Codes: G01N 27/4165 for pH meters
• CPC Class Codes: Y10T 436/10 Composition for standardization, calibration, simulation, stabilization, preparation or preservation; processes of use in preparation for chemical testing
• CPC Class Codes: Y10T 436/100833 Simulative of a gaseous composition
• CPC Class Codes: Y10T 436/102499 Blood gas standard or control

Abstract

In a method for calibration of a pH measuring element whose ion-permeable, hydrophilic polymer layer is brought into contact with an aqueous solution prior to calibration, the aqueous solution is displaced or replaced by a gaseous calibrating medium, and residues of the aqueous solution remaining in the ion-permeable polymer layer. The gaseous calibrating medium contains a known amount of at least one component which is acid or basic in aqueous solution which reacts with the remaining residues of the aqueous solution in the polymer layer, such that a defined pH value is established in the polymer layer, which is employed for calibration of the measuring element.

Claims

1. A method for calibration of a pH measuring element which includes an ion-permable, hydrophilic polymer layer, said method comprising the steps of:

a) contacting said polymer layer with an aqueous solution prior to calibration, said aqueous solution containing stable organic or inorganic compounds as weak acid or basic reacting buffer components;

b) displacing or replacing said aqueous solution by a gaseous calibrating medium, residues of said aqueous solution remaining in said ion-permeable, hydrophilic polymer layer, and wherein said gaseous calibrating medium contains a known amount of at least one component which reacts acid or basic in aqueous solution;

c) enabling reaction of said at least one acid or basic component of said gaseous calibrating medium with said buffer components of said remaining residues of said aqueous solution in said polymer layer, such that a defined pH value is established in said polymer layer; and

d) employing said defined pH value of step c) for calibration of said pH measuring element.

2. A method according to claim 1, wherein said buffer components are inorganic and organic compounds reacting acid or basic in aqueous environment, as well as their salts selected from the group consisting of carbonates, phosphates, phthalates, borates, tartrates, citrates, amines, bis(2-hydroxyethyl)amino-tris (hydroxymethyl)-methane (BIS-TRIS), tris(hydroxymethyl), amino-methane (TRIS), N-tris (hydroxymethyl)-methyl-2-aminoethane sulfonic acid (TES), 4-(2-hydroxyethyl)-piperazine-1-ethane sulfonic acid (HEPES) and 3-morpholinopropane sulfonic acid (MOPS).

3. A method according to claim 2, including adding a neutral salt to said aqueous solution of step a) in order to match the ionic strength of said aqueous solution with the ionic strength of a sample to be measured with said pH measuring element.

4. A method according to claim 3, wherein said neutral salt is selected from the group consisting of NaCl, KCl, and LiCl.

5. A method according to claim 1, including adding a neutral salt to said aqueous solution of step a) in order to match the ionic strength of said aqueous solution with the ionic strength of a sample to be measured with said pH measuring element.

6. A method according to claim 1, wherein ionic or nonionic detergents are added to said aqueous solution in step a).

7. A method according to claim 1, wherein biocides from a group consisting of NaN₃, Mergal K9N, Proclin 300, Bronidox L, and Nuosept C are added to the aqueous solution in step a).

8. A method for calibration of a pH measuring element which includes an ion-permeable, hydrophilic polymer layer and for simultaneously calibrating at least one gas measuring element from the group consisting of CO₂, O₂, SO₂, NH₃, and H₂ S measuring elements, comprising the steps of:

a) contacting said polymer layer with an aqueous solution prior to calibration, said aqueous solution containing stable organic or inorganic compounds as weak acid or basic reacting buffer components;

b) displacing or replacing said aqueous solution by a gaseous calibrating medium, residues of said aqueous solution remaining in said ion-permeable, hydrophilic polymer layer, and wherein said gaseous calibrating medium contains a known amount of at least one component which reacts acid or basic in aqueous solution and further contains the at least one gas component for calibration of said at least one gas measuring element at a concentration corresponding to a normal range of the gas partial pressure of a sample to be measured with said gas measuring element;

c) enabling reaction of said at least one acid or basic component of said gaseous calibrating medium with said buffer components of said remaining residues of said aqueous solution in said polymer layer, such that a defined pH value is established in said polymer layer;

d) employing said defined pH value of step c) for calibration of said pH measuring element; and

e) calibrating said at least one gas measuring element with said at least one gas component.

9. A method according to claim 8, wherein said buffer components are inorganic and organic compounds reacting acid or basic in aqueous environment, as well as their salts of a group consisting of carbonates, phosphates, phthalates, borates tartrates, citrates, amines, bis(2-hydroxyethyl)amino-tris (hydroxymethyl)-methane (BIS-TRIS), tris(hydorxymethyl) amino-methane (TRIS), N-tris (hydroxymethyl)-methyl-2-aminoethane sulfonic acid (TES), 4-(2-hydroxyethyl)-piperazine-1-ethane sulfonic acid (HEPES) and 3-morpholinopropane sulfonic acid (MOPS).

10. A method according to claim 8, including adding a neutral salt to said aqueous solution of step a) in order to match the ionic strength of said aqueous solution with the ionic strength of a sample to be measured with said measuring element.

11. A method according to claim 8, wherein a given CO₂ partial pressure in said gaseous calibrating medium of step b) is used both as said gas component for calibrating said CO₂ measuring element in step e) and as said acid reacting component for calibration of said pH measuring element in step d).

12. A method according to claim 8, wherein O₂ is used as additional gaseous component in step b) for calibrating said O₂ measuring element in step d).

13. A method according to claim 8, wherein ionic or nonionic detergents are added to said aqueous solution in step a).

14. A method according to claim 8, wherein biocides from a group consisting of NAN₃, Mergal K9N, Proclin 300, Bronidox L, and Nuosept C are added to the aqueous solution in step a).