Method and apparatus for measuring localized corrosion and other heterogeneous electrochemical processes

• US 6,132,593 A
• Filed: 06/08/1998
• Issued: 10/17/2000
• Est. Priority Date: 06/08/1998
• Status: Expired due to Term

• Current Assignee: Tan, Yong-Jun
• Original Assignee: Tan, Yong-Jun
• Inventors: Tan, Yong-Jun
• Primary Examiner(s): Bell, Bruce F.
• Application Number:
  US09/093,576
• Time in Patent Office: 862 Days
• Field of Search: 204/404, 205/775.5, 205/777, 205/776.5, 205/794.5, 205/776, 324/71.1, 324/71.2, 324/693, 324/700, 324/425, 324/348
• US Class Current: 205/776.5
• CPC Class Codes: G01N 17/02 Electrochemical measuring systems for weathering, corrosion or corrosion-protection measurement
• CPC Class Codes: G01N 17/04 Corrosion probes

Abstract

An electrochemical method for measuring localized corrosion and other heterogeneous electrochemical processes is described. A multi-sensor electrode namely the wire beam electrode, integrated by coupling all its wire terminals together, is used to simulate a conventional one-piece metal electrode surface in electrochemical behavior. The working surface of the wire beam electrode is exposed to an electrolyte as a conventional one-piece electrode to allow heterogeneous electrochemical processes such as localized corrosion to occur. Electrochemical parameters at local areas of the wire beam electrode surface are detected by means of wires located at those areas. A zero resistance ammeter is inserted between each selected wire terminal and all other coupled wire terminals to measure the coupling current flowing into or out the selected wire, and thus a coupling current distribution map is produced. A high impedance voltmeter is used to measure the electrochemical potential of each temporarily uncoupled wire versus a reference electrode, and thus an electrochemical potential distribution map is produced. A polarization resistance measuring apparatus is used to measure the polarization resistance of each temporarily uncoupled wire, and thus a polarization resistance distribution map is produced. These electrochemical parameters and maps are used to determine the kinetics of heterogeneous electrochemical processes using equations described in this disclosure. This method and apparatus can be used to measure various forms of heterogeneous electrochemical processes such as localized corrosion, cathodic and anodic protection, electroplating, electro-machining, electrotyping and electrowinning.

Claims

1. A method for measuring localized corrosion and other heterogeneous electrochemical processes comprising the steps of:

forming an integrated multi-sensor wire beam electrode system whose working surface simulates a conventional one piece metal electrode surface in electrochemical behavior;

exposing the working surface of the wire beam electrode to an electrolyte as a conventional one-piece electrode surface to allow localized corrosion or other heterogeneous electrochemical processes to occur;

measuring local electrochemical parameters from local areas of the wire beam electrode surface by means of wires located at these local areas using read-out means;

calculating local electrochemical kinetics of localized corrosion and other heterogeneous processes by means of kinetic equations derived based on the wire beam electrode concept.

2. The method of claim 1, wherein the wire beam electrode is fabricated from an array of at least three identical or dissimilar metallic sensors, whose terminals are all coupled together to form an integrated working surface;

whose working surface simulates the shape, the metallurgical composition and electrochemical behavior of a conventional one-piece electrode surface.

3. The method of claim 1, wherein the step of measuring local electrochemical parameters is carried out by operatively connecting each of the individual wire sensors in a wire beam electrode to an electronic/computational system, such that each individual wire sensor is measured for the coupling current flowing into or out of the selected wire sensor, for the electrochemical potential of the selected wire sensor versus the reference electrode, for the polarization resistance of the selected wire sensor, and for the Tafel constants of the selected wire sensor.

4. The method of claim 1, wherein the step of calculating local electrochemical kinetics was carried out by fitting local electrochemical parameters to equation 1:

space="preserve" listing-type="equation">I.sub.ka =I.sub.k exp[2.3(E.sub.sys -E.sub.k)/b.sub.ak ] (1)

or by fitting local electrochemical parameters to equation 2;

##EQU2## or by fitting local electrochemical parameters to equation 3;

space="preserve" listing-type="equation">I.sub.ka =I.sub.gk (

     3)

where I_ka is total electrochemical anodic reaction current which describes overall electrochemical corrosion reaction kinetics over the surface of a selected wire k in the wire beam electrode;

where E_k and I_k are the open circuit potential and open circuit electrochemical corrosion current of the wire sensor k;

where E_sys is the overall electrochemical corrosion potential of the whole wire beam electrode system;

where I_gk is the galvanic current flowing into or out the wire sensor k;

where b_ak and b_ck are the Tafel slopes of wire sensor k.

5. An apparatus for measuring localized corrosion and other heterogeneous electrochemical processes comprising:

an integrated wire beam electrode system whose terminals are all coupled together to simulate a conventional one piece metal electrode surface in electrochemical behavior;

a zero resistance ammeter which is inserted between each selected wire terminal of a wire beam electrode and all other coupled wire terminals to measure the coupling current flowing into or out the selected wire;

a high impedance voltmeter which is used to measure the electrochemical potential of each temporarily uncoupled wire versus a reference electrode;

a polarization resistance measuring apparatus which is used to measure the polarization resistance of each temporarily uncoupled wire.