Concerning the battery charger thing. I must admit that, in dealing with electrolytic systems for 45 years (daily for at least 20 of those years), I've never used a battery charger. I always used plating rectifiers. I may be dense, but I can't see any difference in the marked polarity on a battery charger than that on a plating rectifier. Many of you have used battery chargers, mainly for the sulfuric cell. Did you hook the lead marked positive to the gold plated parts? Did the gold strip? If so, the positive on a battery charger is the same as the positive of a plating rectifier or battery.
Dr.Poe,
As is yours, my main purpose on this forum is to teach. However, due to my attachment to the members of the forum, my 2nd self-appointed purpose is to help protect them. I do what I can to keep them safe and from wasting money. I also search out untruthful statements and try to nip them in the bud. This vast PM subject is difficult enough without creating confusion.
The confusion over the question of, "where is the metal from a negative complex deposited - cathode or anode", still exists. You say anode and most of us say cathode (what if I am right about the battery charger?). I will try to convince you otherwise.
At least once, you said that the gold from a complex negative ion would deposit on the anode and that a simple positive gold ion would deposit on the cathode. Do you still believe this? I can't see that the marked polarity of a battery charger would alter your statement. You are saying that these 2 types of ion species are plated on different electrodes. Wouldn't this infer that, if you had gold and, say, nickel, in a chloride matrix, you would deposit gold (complex negative ion) on the anode and nickel (simple positive ion) on the cathode, simultaneously?? Wouldn't that be a wonderful way to separate metal alloys. Just pick the right solution and you've got a little refining machine. Surely, Wohlwill would have discovered that immediately and his first patent would have been totally different.
Unfortunately, that doesn't work. Metals always deposit on one electrode only, the cathode, no matter what the ion polarity is. Negative ions migrate to the anode but they don't deposit there. To deposit metal, anywhere, the negative ions must somehow be constantly replenished in the cathode film. This is done by mixing (stirring, pumping, heating, u'sonics, etc). It is also done by having a high concentration of metal in the solution. The anode and anything touching it is under a constant, strong, oxidizing pressure from the power supply, which overcomes the reduction needed to deposit metal. However, when you turn the power supply off, the gold would now be able to be reduced and could quickly cement onto the steel anode. Maybe, that's what you and the Ferrells are seeing.
According to Modern Electroplating, the following metals are commonly plated from negative complex ions - Au, Ag, Cu(CN), Zn, Cd, Sn, and Cr. Nickel and copper(acid) are often plated from simple positive ions. In every case, all are plated on the cathode, ONLY.
Dr.Poe,
As is yours, my main purpose on this forum is to teach. However, due to my attachment to the members of the forum, my 2nd self-appointed purpose is to help protect them. I do what I can to keep them safe and from wasting money. I also search out untruthful statements and try to nip them in the bud. This vast PM subject is difficult enough without creating confusion.
The confusion over the question of, "where is the metal from a negative complex deposited - cathode or anode", still exists. You say anode and most of us say cathode (what if I am right about the battery charger?). I will try to convince you otherwise.
At least once, you said that the gold from a complex negative ion would deposit on the anode and that a simple positive gold ion would deposit on the cathode. Do you still believe this? I can't see that the marked polarity of a battery charger would alter your statement. You are saying that these 2 types of ion species are plated on different electrodes. Wouldn't this infer that, if you had gold and, say, nickel, in a chloride matrix, you would deposit gold (complex negative ion) on the anode and nickel (simple positive ion) on the cathode, simultaneously?? Wouldn't that be a wonderful way to separate metal alloys. Just pick the right solution and you've got a little refining machine. Surely, Wohlwill would have discovered that immediately and his first patent would have been totally different.
Unfortunately, that doesn't work. Metals always deposit on one electrode only, the cathode, no matter what the ion polarity is. Negative ions migrate to the anode but they don't deposit there. To deposit metal, anywhere, the negative ions must somehow be constantly replenished in the cathode film. This is done by mixing (stirring, pumping, heating, u'sonics, etc). It is also done by having a high concentration of metal in the solution. The anode and anything touching it is under a constant, strong, oxidizing pressure from the power supply, which overcomes the reduction needed to deposit metal. However, when you turn the power supply off, the gold would now be able to be reduced and could quickly cement onto the steel anode. Maybe, that's what you and the Ferrells are seeing.
According to Modern Electroplating, the following metals are commonly plated from negative complex ions - Au, Ag, Cu(CN), Zn, Cd, Sn, and Cr. Nickel and copper(acid) are often plated from simple positive ions. In every case, all are plated on the cathode, ONLY.