Manny,

 

Thank you. This is getting at what I need to know.  My understanding is that 
aluminum oxide a few nanometers thick forms almost instantaneously on exposure 
of an uncoated aluminum sample to air, and then it’s done.  Does your message 
below imply that exposure to salt fog increases the amount of corrosion of bare 
aluminum alloy, above and beyond that which forms instantaneously upon exposure 
to air?

 

Thank you,

 

-- 

 

Ken Javor

Ph: (256) 650-5261

 

 

From: Manny Barron <[email protected]>
Date: Wednesday, December 4, 2024 at 10:01 PM
To: Ken Javor <[email protected]>
Cc: <[email protected]>
Subject: Re: [PSES] Chromate conversion coatings on aluminum alloy, need for

 

When I worked in the military defense industry many years ago, I specified that 
6061 aluminum alloy be coated in accordance with MIL-C-5541 Class 3, this 
requirement had been around for many many years (1950s ?).  The purpose of the 
thin Class 3 coating was two-fold:  1) to provide corrosion protection, and 2) 
to provide some level of electrical conductivity (although the exact value was 
never specified), while the purpose of the much thicker Class 1A coating was 
primarily to provide robust corrosion protection.

 

But I understand that MIL-C-5541 has been retired and has been replaced with 
MIL-DTL-5541 (2006?).  And the purpose of the Class 3 section is similar to 
MIL-C-5541, except that:  a) other non-hazardous coatings are now allowed in 
order to comply with RoHS, and b) a numerical value is now specified for the 
electrical conductivity requirement along with how to test its compliance.  
Plus there is now an additional requirement for electrical conductivity after 
168 hours of salt-fog testing.

 

This is my understanding of these Mil-Specs. 

 

Manny Barron

 

 

 

 

On Wed, Dec 4, 2024 at 3:36 PM Ken Javor <[email protected]> wrote:

Looking for expert opinion, or better yet an ancient tome describing this 
phenomenon in detail.

 

We have a contractor building a vehicle out of aluminum alloy, with no coating 
of any kind.  Standard practice in our industry is MIL-C-5541 class 3 chromate 
conversion coating when good rf bonding is required.

 

Concern is what happens with no coating.

 

My understanding until very recently was that absent the coating, the aluminum 
oxide that forms would act as an insulator at low voltages. That is, the issue 
of a MIL-B-5087 class H bond (shock hazard – green wire connection) is not at 
issue, because vehicle primary power voltage will punch right through the few 
nanometers of aluminum oxide.  But for class R (rf concerns) the oxide layer 
might look like an open circuit, because the rf potentials are millivolts, and 
cannot punch through. 

 

I procured a couple identical plates of 6061 aluminum, with the intent of 
dipping one of them, leaving the other uncoated, and measuring the difference 
in resistance across bonds with these sheets, using a milliohm meter with 
controlled applied voltage. The controlled voltage is worst case 20 mv, but 
with careful attention, can be held to 200 uV.  Careful attention was applied.

 

To my surprise, I got single digit milliohm resistance across a bond between 
some copper shim stock and the bare, uncoated aluminum plate with no more than 
200 uV applied potential.

 

So the question is, is the chromate conversion only for environmental factors, 
such as salt fog? Or maybe to mitigate dissimilar metal connections? Is the 
fact that it is softer an aid in achieving a gas-tight spot?

 

Why are chromate conversion coatings almost universally applied to vehicle 
sheet aluminum?

 

Thank you,

 

-- 

 

Ken Javor

Ph: (256) 650-5261

 

 

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