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52055
Poor adhesion of Cobalt plating, copper
substrate
May 6, 2009
I am working for an automotive part manufacturer. we are trying to
plate Co onto Cu substrate. the process is as follows, Co strike
layer (0.5 micron 4ASD), then Co plating (3-5 micron, 4ASD). We just
noticed that the bonding strength between Co strike layer and Co
plating was poor but the bonding strength between Co strike layer and
substrate was good. The bonding strength was slightly improved when I
lowered the current density of Co strike layer from 4 4ASD to 3
ASD.
I just wonder what the possible reasons are for this problem and how
to improve it? many thanks.
Adam
Adam Zhang
Plating shop employee - Nagoya, Japan

May 8, 2009
It could be any number of reasons, but the most probable is the
strike is slightly passivating in the air because it is taking too
long to get from the strike rinse tanks to the plating tank. It is
very much like nickel.
There is also a possibility that you have some organic contamination
in the strike tank. pH of the plating tank can be extremely
important. What are you using? I assume that this is a cobalt sulfate
tank.
James Watts
- FL
First of two simultaneous responses -- May 8, 2009
Hello Adam,
lower more down the ASF for the Strike process. Also wondering me
which kind of Co-Strike u r using, are you doing the strike in the
same solution like the proper Co-Process?
Regards,
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Dominik Michalek
- Mexico City, Mexico
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July 2009 -
Seeking Job in Australia, Preferred NSW-Sydney
Area
Hello to all, might anyone read this
inquiry, I'd like to move to Australia for personal reasons.
Therefore I look for a company to hire me as Electroplater.
Have 13+ years experience in Waste Water Treatment, Plating
Technologies, R&D, Project Management, Plant Management,
Service, Training, Analytical. Most experience in
Automotive, PCB and Rotogravure processes. I hope someone
can help me. Thanks in advance.
Regards, Dominik_Michalek at hotmail.com
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Second of two simultaneous responses -- May 11, 2009
Thanks James.
Yes, I use Sulfate bath for Co plating but Chloride bath for the
strike layer.
I was thinking of two possible reasons, pH, as you suggested, and
internal stress. If latter is the case, probably I can do nothing
about it at the time being.
As to the passivation, this is very important information. Many
thanks. May I ask another question regarding to this: how to
re-activate the Co coating? by acid dipping?
Adam Zhang
- Japan
May 15, 2009
Although it is widely assumed nickel and cobalt are very similar
in their metal deposition characteristics, do not be lulled into a
false sense of security; they do have a lot of subtle
differences.
For instance, cobalt tends to be more highly stressed than nickel
when deposited from comparative solutions, so using cobalt chloride
may be one of your problems. Personally I would suggest you use a
cobalt sulphmate strike - since this is not a well known system I
suggest you base your formulation on a nickel sulphamate
strike.
I would also tend to use a sulphamate bath in place of a sulphate one
for the same reasons as above.
Regarding reactivation of cobalt, I have never had any real problems
with it, with the caveat that I never let it really passivate. If you
are having a problem, it may be worthwhile you reactivating it in the
plating bath by using an anodic "etching" with about 2ASF for about
30 seconds followed by conventional cathodic deposition. This will be
dependent on teh bath pH, so I would suggest you use a lower pH
system in preference to a higher one.
One thing I found was that the conventional nickel brighteners are
nowhere as good with cobalt.
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Trevor Crichton
R&D practical scientist - UK
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