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Letter 10897
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Anders Sundman |
Patrick,
Are you following the stict steps of activation in 3:1 HNO3-HF to red fuming and the dicromate? Are you controlling the HF content closely?. Your acid copper doesn't seem to be the problem. Please give us more info to better help.
Regards,
Guillermo Marrufo
Monterrey, NL, Mexico
Thank you very much for your advise.
As pretreatment I've been using this cleaning process for both titanium cathode and copper anode:
1. Thorough washing in detergent solution
2. NaOH 10%
3. H2SO4/HCl 10%
Rinsing after each step.
After your replies I've also been trying the activation process with 1:3 HNO3:HF solution. There was a reaction taking place with gas formation(green). It was obvoius that the solution etch the outer layer of the titanium electrode, it was smaller afterwards. Is the purpose to remove a TiO2 layer?
Unfortunately the plating wasn't much more successful afterwards. I still get the very porous dark copper that falls apart. It seems like there is a thin bright copper layer right next to the cathode, but when running the process for a longer time it is also converted into this porous material. Two times I've succeeded getting a thin bright deposit, but only when running the plating for a short while.
I have the option of depositing another metal layer on top of the electrode and now I'm thinking of what metal to use. Platinum or palladium should be good I guess, I want it to be a good copper seed material and at the same time very inert in the electrolyte. Another option may be to make the whole electrode in stainless steel. What materials are the best when it comes to copper seed properties?
One last question, what current density range should be used for a bright solid deposit according to you?
Best regards,
Patrik Moller
- Lund, Sweden

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