Hi, I'm new, so please take my lack of experience into consideration when reading my response.
The original poster earlier in the thread mentioned going with a sulfuric cell instead. Do you have a way to test out a sulfuric cell to see if it would be suitable? I ran a small-scale test of some very low grade pins. It was meant to be a small-scale test, but I ended up processing over 1kg, through a <100mL cell. Having a multimeter inline, in Current reading mode, really helped visualize how strong or weak the reaction was going once the solution got cloudy and dark. Things I'm uncertain about in your case:
1. the inside surfaces of hollow items - I don't know how important it is for there to be a "line of sight" from the gold surface to the electrode. I wonder if only the outside surface will deplate.
2. The parts where the plating is not exposed to air - I very much doubt that this plating will be removed.
3. chemical compatibility - I know copper is safe enough in Sulfuric acid, and I didn't have any problems with the nickel-plated copper with partial gold pins that I experimented with. But literature says that copper, and metals above it (more reactive) in the reactivity series are weak to sulfuric.
I think where "AP" comes into play, is if you have scrap which is mostly copper, since you can recover the copper salts that crash out, "recycle/refresh" the solution, and fairly cheaply be ready to add more pins to digest.
Hmm, so after typing that out, it seems like we have several good ways to deal with copper base metals. I'm not sure what the experienced consensus would be on ferrous base metal gold plated things.