Active Member Posts: 4692 Joined: March 1st, 2011, 7:56 pm Location: Decatur,Ala. November 4th, 2011, 8:49 pm
did you add water to the AP solution? if you are relying on H2O2 as your only source of oxygen then the white crystals are more than likely tin(II)chloride.this poses no problem to the process.the best advise i can give you is for you to cap everything and stop the process and read up on the AP process here on the forum.how large is your reaction vessel.how large is the batch you have run.do you have an air supply to the solution.answer these question for a better answer on perhaps your next step.
"knowledge is power"
joekelly Member Posts: 7 Joined: November 4th, 2011, 5:36 pm Location: Portland, Oregon November 4th, 2011, 10:29 pm
Active Member Posts: 4692 Joined: March 1st, 2011, 7:56 pm Location: Decatur,Ala. November 5th, 2011, 1:17 am
after that much material has been run through such a low volume of solution im surprised your getting any reaction at all,especially without a fish bubbler.your solution is loaded with tin, it probably has been to the saturation point a few times. as you add H2O2 it also dilutes the acid somewhat and allows tin to precipitate out as a white crystal.when you start back (please read and be familiar with the process first) add fresh hcl acid (muriatic acid) and used solution in these proportions new hcl to used solution 3:1. 3 quarts fresh acid and 1 quart used solution and add a fish bubbler as oxygen is the key that drives the reaction.first filter all solids you have now from solution (white stuff and gold flakes).put this in an old pyrex coffee pot and add a cup of fresh hcl acid and warm it up. do not do any of this indoors without a fumehood and never in your living space.if the white stuff is tin(II)chloride it shouldnt change much but this will clean any tin metal or copper metal in your foils.let it all settle and decant slowly into another glass vessel so you dont pour out any gold foils.dont worry about getting it all,its ok to leave a little.next add water and warm till a slow boil then remove from heat and let everything settle.decant this slowly into another glass vessel and neutralize with baking soda slowly then discard.anything thats left is now ok to refine even if it still has white crystals or not as it will not effect the process of dissolving with hcl/cl and you will leave it behind in the filter anyway.
"knowledge is power"