Method of monitoring constituents in conversion coating baths

• US 5,753,101 A
• Filed: 08/01/1996
• Issued: 05/19/1998
• Est. Priority Date: 08/01/1996
• Status: Expired due to Fees

• Current Assignee: Technic, Inc.
• Original Assignee: Technic, Inc.
• Inventors: Ludwig, Frank A.
• Primary Examiner(s): Gorgos, Kathryn L.
• Assistant Examiner(s): Leader, William T.
• Application Number:
  US08/690,769
• Time in Patent Office: 656 Days
• Field of Search: 205/81, 205/82, 205/83, 205/101, 205/794, 205/794.5, 205/780, 205/781, 205/786, 148/241, 204/402, 204/412, 204/434
• US Class Current: 205/781
• CPC Class Codes: C23C 22/77 Controlling or regulating of the coating process
• CPC Class Codes: G01N 27/49 Systems involving the determination of the current at a single specific value, or small range of values, of applied voltage for producing selective measurement of one or more particular ionic species

Abstract

A method for monitoring the constituents present in conversion coating bath solutions. The method involves using specific ac and dc voltammetry and using platinum or other noble metal working electrodes. First, a selected dc potential is applied to a working electrode which has been subjected to pretreatment and which is present as an in-tank sensor in the bath being analyzed. A constant ac signal is superimposed on the dc potential. The dc potential is then swept over a chosen range at a selected sweep rate. The various constituents in the bath are then monitored by measuring dc current and the ac current at one or more reference phase angles with respect to the constant ac signal between the working electrode and a reference electrode as the dc potential is varied. The resulting dc and ac spectra provide a useful measurement of the make-up of the constituents in the bath solutions.

Claims

1. A method for monitoring the constituents present in a conversion coating solution used in a non-electrolytic conversion coating process wherein a conversion coating is applied to a metal substrate, said method comprising the steps of:

(a) applying a selected dc potential to a working electrode which has been subjected to annealing and anodic pretreatment, said working electrode being positioned within said solution containing said constituents, said dc potential producing a dc current; and

wherein hydrogen gas is produced at said working electrode and said conversion coating precipitates at said working electrode;

(b) superimposing a constant ac voltage on said dc potential applied to said working electrode, said ac voltage having an amplitude and a frequency and producing an ac current;

(c) varying said dc potential at a chosen sweep rate over a chosen range; and

(d) measuring said dc and/or said ac current or a harmonic of ac current at one or more reference phase angles with respect to said constant ac voltage between said working electrode and a reference electrode positioned within said solution as said dc potential is varied over said range, said measurement of dc and/or ac current in relation to varying dc potential being expressed as a dc and/or an ac current spectra which is used to determine and monitor said constituents in said solution.

2. A method for monitoring constituents present in a solution according to claim 1 wherein said solution is a zinc phosphate, chromate, iron phosphate, or manganese phosphate conversion coating solution.

3. A method for monitoring constituents present in a solution according to claim 2 wherein said solution is a zinc phosphate conversion coating solution.

4. A method for monitoring the constituents present in a solution according to claim 3 where the working electrode is platinum and anodic pretreatment of said working electrode comprises treating said working electrode with a dc anodic potential of about +2.0 volts for 5 seconds.

5. A method for monitoring the constituents present in a solution according to claim 1 wherein said working electrode is selected from the group of noble metals and noble metal alloys consisting of platinum, gold, indium or alloys containing a major percentage of a noble metal.

6. A method for monitoring the constituents present in a solution used in a conversion coating process according to claim 5 wherein said working electrode is platinum.

7. A method for monitoring the constituents present in a solution according to claim 5 wherein, prior to said anodic pretreatment, said noble metal or noble metal alloy of said working electrode is annealed in an oxidizing flame or gas furnace at temperatures just below the melting point of said noble metal or noble metal alloy.

8. A method for monitoring the constituents present in a solution according to claim 1 wherein said anodic pretreatment of said working electrode comprises treating said working electrode with a dc anodic potential up to +3.5 volts for 2 to 30 seconds.

9. A method for monitoring the constituents present in a solution according to claim 8 wherein said working electrode is platinum and said anodic pretreatment of said working electrode comprises treating said working electrode with a dc anodic potential of about +2.0 volts for 5 seconds.

10. A method according to claim 9 wherein said solution comprises nitrite as a constituent and said nitrite constituent is monitored, and wherein said selected dc potential applied to said working electrode is a dc sweep signal which is swept from +2.0 volts to -1.0 volt and back to +2.0 volts at a rate of 50 mv/second.

11. A method for monitoring the nitrite constituent present in a solution according to claim 10 wherein said constant ac voltage superimposed on said dc potential is a sinusoidal waveform having an amplitude of 25 mv root mean square and a frequency of 500 Hz and the second harmonic response current is measured.

12. A method for monitoring the nitrite constituent present in a solution according to claim 11 wherein said reference phase angle is 0 degrees.

13. A method for monitoring the constituents present in a solution according to claim 1 wherein said selected dc potential applied to said working electrode is a dc sweep signal which is swept over a maximum range of about +2.0 volts to -2.5 volts and reversed to voltages of up to about +2.0 volts at a rate of between about 10 to 1,000 mv/second.

14. A method for monitoring the constituents present in a solution according to claim 1 wherein said constant ac voltage superimposed upon said dc potential is a sinusoidal waveform having an amplitude of between 5 and 100 mv root mean square and a frequency of between about 30 to 20,000 Hz.

15. A method for monitoring the constituents present in a solution according to claim 1 wherein said reference phase angle is between 0 and 90 degrees.

16. A method according to claim 1 wherein said solution is a zinc phosphating solution comprising nitrite as a constituent and said nitrite constituent is monitored, and wherein said selected dc potential applied to said working electrode is a dc sweep signal which is swept from +2.0 volts to -1.0 volt and back to +2.0 volts at a rate of 50 mv/second.

17. A method according to claim 1 wherein said solution is a zinc phosphating solution comprising nitrite as a constituent and said nitrite constituent is monitored, and wherein said constant ac voltage superimposed on said dc potential is a sinusoidal waveform having an amplitude of 25 mv root mean square and a frequency of 500 Hz.

18. A method according to claim 1 wherein said solution is a zinc phosphating solution comprising nitrite as a constituent and said nitrite constituent is monitored, and wherein said ac current or a harmonic thereof is used to determine and monitor the nitrite constituent.