Thank you for your content.Over the years, it has been highly enjoyable and satisfying.Watching you do your processes, Something about your purification process. Separating the amalgamit's really is therapeutic. I have been watching for over a decade now.Probably not as long as others but long enough to say I consider you a brother... Much love and all the blessings to you and yours!!!
It’s not the utensils. Thieves will re-upload my videos as their own creation. Early on one person had downloaded my entire video collection (even the one of my wife receiving her wedding anniversary gift) and re-upload my videos to their channel. I was baffled and didn’t realize you could do that. Caused me to stop posting for six months. But then I discovered how to report it and get them removed. Now I have “content ID” and any of my videos that get re-uploaded by thieves, gets reported to me. So you see, the utensils are NOT what they’re after. It’s the highly valuable video content that they want. And the only way I can think of to prevent the theft is to brand my videos. Like I said. It’s a giant pain, wish I didn’t have to do it. But this is the world we live in. People constantly looking to get something, for nothing.
I really enjoyed the Darth Vader imitations while emptying the water in the sink, but loved the visuals with the silver creamer melts, Loved tonight's video!!! Oh ya I met a young man named Sree last week at work. didn't think I would ever meet someone with that name.
Sodium chloride brine electrolysis would negate the need for inquaurtation. It converts the gold and other constituent metals into a very finely divided mud. I don't know how silver would react to the nacient chloride reaction, but it takes the gold plating layers off of plated phosphor bronze quite readily. There is no need to process the bulk of the core base metals, so there is also the effect of concentrating the gold content by leaving much of the base metals behind. If nothing else, it reduces the requirements for acids in the processes afterward.
I have had difficulty, in the past, converting Silver Chloride into a viable aqueous suspension, that is suitable for dropping out clean Silver. It's doable, just a pain. For what it's worth.
Man!!! You make it look so easy, Brother! I don't know if I'm going to live long enough to get to where you are now! Seriously, you are a ROCK STAR, in Alchemaic Sciences!
It is so satisfying watching u do the whole process of refining the gold, I could watching u for hours explaining it all u r so good at refining silver and gold, love your channel it's amazing and awesome 👌 👏 👍 fantastic job.
I already know you wanted to throw one of those bracelets in the batch to push your estimated yield up to 93.3 😉. As for the refining, very well done sir! That gold looked clean on the first drop!
I was looking at Tomoko's Enterprize channel and saw where he got some silver crystals from you and made a king about 3 years ago and I saw where you started a chess set about 6 years ago. Someone on that channel said it would be neat to see a silver and gold chess set. Still just learning refining, using a torch or a home made furnace, home made vacuum chamber, how to identify the jewelry and everything else. It takes time learning all that and casting the metals is an art. It was nice to see some of your crystals get cast into something.
I like how at 29:24 when you add the first spoon of SMB and the first gold starts to precipitate, all he ice in the beaker jams up to the top of the liquid.
@@johnschruben3586 I remember the video, mrs sreetips was really upset. To be fair I'll have to add, that it was just a reproduction of a 20 Dollar gold coin, not a original coin wich would have had numismatic value. If I remember it right, sreetips once mentioned he does not melt or dissolve coins. There is no need to refine them since the issuing county guarantees for the right precious metal content of the coins, so it's a known quantity of precious metals to calculate with.
I also had an idea....... A Centrifugal separation using a Maytage washing machine, that has a Stainless Steel drum and no agitator in the middle to get in the way. Waiting for gravity to drop parcipitates is almost unendurable. At my age time is a valuable commodity! What are your thoughts? Comercial centrifuges can't do large capacity solutions. I figured a way to be able to use 8,1,000 ml beakers at a time, in the drum of the washer. They would be able to pivot as the washer sped up.
Hi. I'm new here and really love your channel. I have a question though, maybe 2. I have a lot of e-waste material like mainboards and old pci cards and old gold painted watches and so on, kilos and kilos. I figured I remove the components that could be of value as they are, such as EPROMs, Coils, Tantalum Caps, Inductors and some ICs. Most of the other components, such as resistors and caps are not worth a lot and I left them on the boards. Now the idea is to break the boards apart so they fit into my plastic container in order to give it a chembath so I can extract all the metals from the boards and the 9k jewlery. From the videos I've seen so far I know that Nitric Acid will break down every metal, except Gold if I just give it enough time and some bublling action or heat it up, please correct me if I'm wrong here, maybe I missed something but as far as my monkey brain understands, Nitric Acid breaks the metals such as Tin, Silver, Copper and Aluminum (or Aluminium) apart. I suspect there could be some other metals on the boards or inside the watches that don't get dissolved in Nitric Acid? Anyways, if I'm correct the Nitric Acid should take out everything that isn't Gold, I would pour the solution into another container for later possible silver extraction (using copper rods). Once I see no more stuff reacting with the Nitric Acid I would prepare 3 parts of Clohidric Acid and 1 part of Nitric Acid in order to obtain the Agua Regia to dissolve whatever gold is left on the boards/jewelry. Bubble action again, or heating it up to make it faster ofc, and transfering the solution into another container until there is no more yellowy reaction going on in my fist container (there should be no gold left then I guess). I would then add sodium metabisulfite to precipitate the gold from the agua regia solution and heat the obtained powder in my table furnace into a blob. Please tell me if the plan is correct and I understood everything correctly, or maybe explain a different, better approach. Could I maybe directly make Agua Regia, extract all metals with it and then just precipitate the gold and toss teh rest? I don't trust ChatGPT and don't wanna blow up my workshop xD. Really looking forward to a professional opinion from someone that does this stuff by the day.
I don't do this by the day, but I think I am pretty knowledgeable about this. Nitric acid will also leave Pt group metals (PGMs) next to the gold. As far as I know, those are pretty rare in computers, so no real need to worry about it, just so you are aware (and don't toss them away). Basically, you are correct. You will get better results with the first method, but the second method (direct to AR) is quicker, but you will toss silver (and possibly PGMs).
Missed something on inspection! I think what you didn't catch in the melt showed up in the filter! Nice to see the strait forward process for high purity end result!
Have you ever thought about melting metal with a solar death ray? People frame up a lense from an old big screen tv and use it to focus the sun. It might be hard to control but it would save on gas. Also you could do larger amounts, the beam is about an inch wide and will slice through anything.
Aqua regia does dissolve lead (just about anything), but the added sulfuric acid will precipitate lead as lead sulfate (highly insoluble). Besides that, silver will precipitate as silver chloride as that also is insoluble, one of the reasons to remove it with nitric acid before going to AR.
Afternoon Gunny! Have you ever had issues with the inquartation process? I'm working with some 18K, maybe a bit better. It doesn't seem to want to mix well with the copper I'm using for inquartation. I've melted and stirred it twice now and I'm still getting copper shot in my quenching pot. Any ideas?
QUESTION: If I have been paying attention well enough, could you alternatively take the inquarted gold/silver to your silver cell for extraction of the gold, and then take the gold residue straight from the silver cell feed bag into the aqua regia process for refining (with associated rinses and sulfuric acid lead removal step)? Thank you for all your educational videos.
Question for you @sreetips which you may have addressed in a past video. How long could you store the gold in solution after dissolving the gold in aquaregia (spelling?) and boiling off the excess nitric? Can it be store indefinitely or is there a time frame it should be precipitated out?
@@sreetips Good to know. Thank you sir for being such a great teacher, my kids and I quite enjoy your video's! My oldest will be starting chemistry soon and is hoping to be able to use the knowledge she has gathered from watching you to bolster what she is going to be learning in school.
That’s fantastic. I was interested in chemistry when I was in school fifty five years ago. Had a small chemistry lab set up in my basement. I took a chem class in high school and got a D. It was too much study and memorizing. I wanted to get down to business and do reactions. My channel is an extension of that. Now that I’m grown up, I can do what I love.
how do you work out the cost of refining the gold and other metals? not so much the buying of jewellery, the flux and acids and materials used while refining?
I don’t know those costs. We buy gold so very cheap at local sales that those costs don’t matter. I wish I could publish some videos on that but Mrs sreetips has asked me not to
Yard sales and estate sales, mostly. People are clueless about gold and silver. They believe, incorrectly, that paper dollars are more valuable. This misconception creates some fantastic buying opportunities.
@@sreetips That's awesome! How much cash do you think it would take to setup a small refinery operation for a beginner using home-made stands and thrifted wares? Of course I understand there are some pretty hefty premiums for quality glass, but I like the way you've been able to seemingly keep your overhead cost for equipment moderate.
I accumulated it as I needed it. Type lab glassware on eBay. Sometimes you can find a bunch for cheap. The first thing you need before glassware is a fume hood. No way to safely do these reactions without one.
@@sreetips Understood! These are incredibly damaging substances for every part of the body that I'm aware of! Thanks for all your help and thanks for making content of these scientific processes. That SO2 reaction was TO DIE FOR!
Quick question regarding your calculations. Where is the 1.265 for 14K and 0.635 for 10K derived from? If you're inquarting, would it not be simply taking the weight of each Karet multiple it by 25% to get the amount of silver would be needed to lower the Karet for recovery via HNO3?
@@sreetips I see. Correct me if I am wrong. If I have a 38 gram of 14K bracelet. The gold content of that bracelet can be calculated by part to whole division. 14k/24k equals 0.58 or 58% of pure gold. Then would you inquart 0.145 of silver to knock down the karat?
38g x .583 = 22.15g pure gold times 3 equals 66.45 - (38g - 22.15) = (66.45 - 15.85) = 50.55g x .95 = 48.02g sterling to properly inquart 38g of 14k. Or just multiply 38g time 1.265 = 48.07g sterling to properly inquart 38g of 14k. The last digits are insignificant.
Hello Mr. Sreetips. Silly question here. Can gold somehow be in gas form? I know it's stupid, but I feel like some of the gold is flying away of the beaker in gas form. Is it possible to place a stannous chloride soaked paper on top of the beaker during the aqua regia process in your next videos to check this? Thanks.
Can you inquart with gold plated scrap? I've seen you use several base metals to inquart. Using scrap plated material could allow you to recover the gold more easily in the plated stuff and provide the needed base metal.
Thanks for sharing with us Sreetips 🤠 Excellent Work 🐉 God Bless 🙏 I can't wait to get out and do some metal detecting at the lakes here Find some scrap gold.
Yeah, I have been guilty of getting too excited and jumping the gun. The results are that you end up spending even more time and chemicals redoing. Definitely frustrating.
Is the silver incourtation absolutely necessary for the acids and heat to purify the gold? It won’t chemically react the same I’m assuming? Have you ever tried??
Putting scrap gold directly into Aqua Regia can be done. But it makes a very dirty solution and passivation can occur (hard crust of silver chloride forms and shield the metals from the acids. Both problem are completely eliminated with inquartation.
Have you ever extracted and refined gold from gold ore? I know there’s several videos on TH-cam be about it. It would be interesting to see your procedure.
Hello me again, I have a question i dont think you have ever addressed before. What happens if you have your loaded aqua regia with gold , and just leave it to evaporate ? No MSB or such, just let it air dry out? If i was to guess it would crystallize, but again i,m guessing. Thanks
Dear sir : Ty for your excellent video , I was wondering why u don't use the urea to kil the nitric, what u do instead of using urea? Thank you for your reply
Incremental nitric dosing; adding just the right amount of nitric to just dissolve the gold. But if I do over-shoot with nitric, then the best method, by far, is evaporation down to a syrupy stage until all the excess nitric has been driven off. Adding urea to kill excess nitric is antiquated and no longer used by modern refiners.
@@sreetips I saw a label on your bottle of the stannous cloride in the video written on it the ingredients of the that cloride but it wasn't readable, Would you please provide me with that ingredients or how to make a good stannous cloride to test the gold, That would be very kind of u sir.
QUESTION. I have a vintage class ring, 1944. The inside is stamped “BALFOUR GOLDFLEX”. After watching a boatload of your videos I can tell you know way more than you let on, lol. Do you happen to know ow what goldflex is? Thanks
@@sreetips thanks for the response. I’ve seen too many conflicting descriptions on the internet. I’ve seen people say it’s nothing, but I’ve also seen some say it’s 8k. It was definite worth asking someone with your kind of experience in the precious metals, though, so thank you. Love watching your refining videos. Keep on keeping on!
Is it safe to pour Nitric acid into a hot beaker after a decantation? I heard that there could be risk of beaker crack when adding cold liquid into hot beaker. This is what bing copilot says: " For standard laboratory glassware like borosilicate glass, which is designed to withstand thermal stress, a temperature difference of around 100°C (212°F) can still be risky. If the beaker is at 150°C (302°F) and you pour a liquid at 0°C (32°F), the sudden change can cause it to crack."
If there’s liquid in there, I’ve never had a problem. But I did sit a two liter beaker on the heat for just a few minutes dry. When I added some liquid it cracked. So I’d say never add liquid, hot or cold, to a hot dry beaker.
Hello teacher I'm doing the same thing in Korea. These days I have a problem. In winter, the purity was 99.9%, but as the weather warmed up, silver started to show. Teacher you put ice in the video, is this related to Agcl?
Hello, just came across your channel. May I ask exaclty what it is that you are doing? Are you taking gold from junk-electronics and refining it? Or are you growing gold in a home lab?
I’m refining the gold from pieces of broken and scrap karat gold jewelry. I buy the scrap gold at local sales, then refine it and my videos. It’s my hobby.
Kevin I'm curious, have you ever attempted an AP base metal extraction in lieu of a nitric extraction after inquartation? I would imagine it costing a LOT less in reagents at the cost of a week bubbling outside. Just a thought for a potential video. It's how I've done mine (on smaller scales) to save from spending the pretty penny on nitric or making enough to do a batch.
@@sreetips ya I don't know why I didn't think of that on your end (cause you always work with silver), I always use copper myself for inquartation when needed.
Amazing that the I've cubes sink to the bottom whole gold in solution nut as soon as you release it the ice cubes fly to the surface Great work as usual
New to the channel and fascinated with it all. I’m sure it’s been explained elsewhere, but I’m wondering if you precipitate the silver back out of solution? Is it difficult? Is it worthwhile? Is it just the cost of doing business when you refine the gold? Edit: never mind I think I need to check out the silver videos..
He takes the silver waste and either runs it thru a silver cell or cements it out in copper to be refined in a stock pot refining video very little goes to waste on this channel you will enjoy his catalogue of videos for sure look for his silver cell videos they explain the silver recovery I hope you remember to take breaks periodically as u get stuck into the videos
What were the little white blobs, you pulled out with a tweezer? Just curious. It looked like Borax. I have the same thing occur. I'm going to melt some 14K and 18K today. Thought I'd try the Copper inquartation you demonstrated.
@sreetips Absolutely! Fume hood is robust! Also a full face respirator, gloves and Flame and Chem resistant lab coat! I watch your tutorials, Gunny. Hard to miss the warnings at the beginning of each one! I'm glad for them and your safety precautions. I've looked at other sites, occasionally. It is distressing to see some sticking their hands in a beaker with fuming Nitric and not be wearing gloves! YIKES! Also the guys decanting catalytic ceramics. No respirator, no gloves, just sucking in the dust! Unbelievable! I am in the practice of studying each process, researching ect. As well as SREETIPS, the Gold Refining Forum is a solid referencing source. Thanks for that as well! It was your suggestion to me, to become a supporting member. Your videos are extremely well done and you always give us a heads up, when a potentially energetic reaction will occur. That's why I'm a devoted follower. You do it RIGHT!
Would you concider to use metric numbers in length as well not just only in weights? When I hear 7 inch, it doesn´t mean anything in Europe. Thank you Mr Sreetips. Greetings from Sweden.
Good afternoon again good sir. Quick question, as always lol. What ratio would you say you use when adding sulfuric acid to precipitate and lead? Or are you just adding a squirt, so to speak? Thank you as always, can never get enough of these videos. One more question. When inquarting, say you don't have enough gold to make 6k gold (I have some grips for a 1911 I won at auction for 120 bucks that have 20% of their weight being made up of 8k gold and I don't have enough gold to get to 6k)... is there much harm in having a higher ratio of silver to gold?
@@sreetips I have found that my autism often leads me to not fully communicating all the important information, my apologies for that. I should have noted the 8k gold is 'welded' on top of the silver. It could just be my limited knowledge but I don't see a real option other than melting it all together. It is a very ornate design going across the entire surface so cutting it out isn't an option.
If the 8k gold is welded to a piece of silver, then I’d just boil the whole thing in dilute nitric. The silver will dissolve completely, the 8k gold is low enough gold concentration that the nitric will get all the silver out of the gold too. If you boil it long enough
Are the torches/burners you use oxy-acetylene? Could it all be done using a metal melting furnace? Also, is the burner you use with the ceramic and glassware an induction burner or coil?
Another AMAZING educational efficient video. You r the BEST on tha Tube!!! 💯💯💯 I do have something I hope you can help me out with, I unfortunately do not use Nitric due to cost and availability, what options/substitutes do u recommend inplace of the Nitric boils for refining karat gold? I usually dissolve in acid peroxide bleach, and just tested a new method of Potassium Nitrate and HCL as a Aqua Regia substitute, if I can find a sub for the Nitric boils I'll b SUPER happy. Thanks in advance, speaking on behalf of your viewers we REALLY appreciate you sharing your knowledge and experience! I can't imagine how many you have educated! You are truly a gift to us! We can not thank you enough! God Bless, I wish u and your family all the best!
What's your ph on the orange disolved hold solution and the clear solution, post precipitation pre rinse? Just wondering how acidic it still is. How much it drops during precip.
Sreetips: Regarding Sterling silver, if it is 88-90% silver, what price per ounce, as a percent of spot, would you pay for silverware and still consider it to be a good deal? Also, when appraising silverware, what would you deduct for components that are not sterling, like knife blades? Thanks!
80% of spot. I figure 10g of sterling for the weight of the handle. But if you end up paying 100% it’s still a good deal because silver is grossly undervalued.
Also, if your stannous tests smoke yellow, its because of excess nitric correct? Thats what i believed anyway, i added a lot of SMB (to avoid Urea), and my 1st drop had gray/brown crystals with gold mud inside rhem and beside them. Luckily hot water fixed it all in the end, but thats the 2nd time in hundreds of runs over years that i had those crystals, first time a decade ago, they were green/yellow crystals. This time, I just remember my stannous test smoking yelleow, and having to add a whole lot of SMB before any color change or gold drop. It was a scary moment that still has me puzzled 5 days later. I tell myself it was to much nitric (im usually using Sodium Nitrate), and then to much SMB to neutralize it. But im honestly unsure. Good news is you rarely, or likely never lose the gold in solution forever. But sometimes you must worker 10x harder to get the gold back because you made a mistake. And that day i made some mistake. But the fix was easy, fortunately for me.
I use evaporation to drive off excess nitric. It’s far superior than adding reagents to kill excess nitric. It’s easy to do, it works every time, just takes a little longer.
I'm getting a yellow precipitate coming Ng from my gold while dissolving in the aqua regia. Do you have an idea as to what this is? Does it contain any gold?
Probably silver chloride. I just filter it out, pass it through the same filter a second time if it’s still cloudy. Then I add the filter to my paper storage for later processing.
I was thinking it might be similar to the way they get it from spark plugs. I was just curious cause I’m in the pool and Spa business and we throw away hundreds of these cells every year thank you sir.
Refining platinum group metals requires a lot more chemistry and highly specialized equipment. Gold and silver are like a cookie recipe compared to PGMs. Not suitable for a hobby refiner to risk it.
I dig how ya monogram EVERYTHING, I have a looooong name, having caught the names of 3 U.S Generals.. So "NOT YOURES" in sharpie on all my tools/items will usually suffice ... And if cans/bottles full of un-labeled chemical/organic solvent: "NOT BOOZE" And if within $pendy bottle of Tequila: "NOT YOURE BOOZE"...;) I really DIG watchin ya work away in youre own personal Alembic. Its truly fascinating stuff. Ive picked up quite a bit from yee, even though Im not in the precious metals game whatsoever (Aside from firearms/Hand-loading ammo I suppose?..;)
Back to the yeller stuff. Love the colors of both the blue and red/yellow and then to the bright yellow. Last two nitric boils could have been saved to reuse. $ wasted...
Excuse My ignorance, so allá these si refining, same as "growing silver cristals" you are not creating artificially the environment so the silver or gold can "grow" it's a refinament technique where You end up with les matireal but more puré, rigth ? You don't start with 200 grms and end up with a 1,3 kilos of silver. Please correct me, i want to learn.
I refine gold. I use sterling silver, that I buy at estate sales, to refine the scrap gold. I recover the silver from that, melt into shot, and run it through my silver cell. Silver is a by-product of my gold refining. The cell converts the impure silver (about 980 parts per thousand silver) to high purity four nines fine (9999 parts per ten thousand) pure elemental silver metal. So I’m refining the impure silver, into high purity silver, not creating silver out of thin air. When it’s full, I harvest the pure silver crystal, put it away and forget about it. Then I repeat the whole thing again.
30:59 Thank you for your informative and thorough content! Can you point me to books or websites that have written directions on refining karat gold into “pure” gold? Thanks again.
Ran the numbers for those who are thinking of bidding on the bracelets. The melt value of the Charleston bracelet is about $450, and the melt value of the San Marco is a bit over $460. Don't low-ball the senior chief!
Thank you for your content.Over the years, it has been highly enjoyable and satisfying.Watching you do your processes, Something about your purification process.
Separating the amalgamit's really is therapeutic. I have been watching for over a decade now.Probably not as long as others but long enough to say I consider you a brother... Much love and all the blessings to you and yours!!!
Thank you
I just wanted to bring your attention to the fact that your ice cube tray did not have your name on it .
Painting my name on everything is a giant pain. Wish I didn’t have to do it.
Thank you
Lmfao!!! Well spotted
You really have to do that step???? I didn't think your utensils were so sought after @@sreetips
It’s not the utensils. Thieves will re-upload my videos as their own creation. Early on one person had downloaded my entire video collection (even the one of my wife receiving her wedding anniversary gift) and re-upload my videos to their channel. I was baffled and didn’t realize you could do that. Caused me to stop posting for six months. But then I discovered how to report it and get them removed. Now I have “content ID” and any of my videos that get re-uploaded by thieves, gets reported to me. So you see, the utensils are NOT what they’re after. It’s the highly valuable video content that they want. And the only way I can think of to prevent the theft is to brand my videos. Like I said. It’s a giant pain, wish I didn’t have to do it. But this is the world we live in. People constantly looking to get something, for nothing.
These inquartation melts are always so satisfying to watch plus the refining process is fascinating 👍🏻
I really enjoyed the Darth Vader imitations while emptying the water in the sink, but loved the visuals with the silver creamer melts, Loved tonight's video!!! Oh ya I met a young man named Sree last week at work. didn't think I would ever meet someone with that name.
"Mrs. Sreetips has directed me . . . " LOL! She Who Must Be Obeyed!🐞 We all have one.
Sodium chloride brine electrolysis would negate the need for inquaurtation. It converts the gold and other constituent metals into a very finely divided mud. I don't know how silver would react to the nacient chloride reaction, but it takes the gold plating layers off of plated phosphor bronze quite readily. There is no need to process the bulk of the core base metals, so there is also the effect of concentrating the gold content by leaving much of the base metals behind. If nothing else, it reduces the requirements for acids in the processes afterward.
I have had difficulty, in the past, converting Silver Chloride into a viable aqueous suspension, that is suitable for dropping out clean Silver. It's doable, just a pain. For what it's worth.
Man!!! You make it look so easy, Brother! I don't know if I'm going to live long enough to get to where you are now! Seriously, you are a ROCK STAR, in Alchemaic Sciences!
That gold in aqua regia... Wow. It's gorgeous!
Was about to go to bed and got the alert I'm definitely not going to bed yet lolol 9:45 pm was when it alerted me my favorite on TH-cam by far
It is so satisfying watching u do the whole process of refining the gold, I could watching u for hours explaining it all u r so good at refining silver and gold, love your channel it's amazing and awesome 👌 👏 👍 fantastic job.
How much do you think you spend on one batch of converting impure to pure gold?(not counting the metals) Gas for torches, liquids, electricity, etc.?
I’d say around fifty bucks, all in
Wow thats actually not bad! I would assume you try to buy your reagent in bulk.
I already know you wanted to throw one of those bracelets in the batch to push your estimated yield up to 93.3 😉. As for the refining, very well done sir! That gold looked clean on the first drop!
It’s mesmerizing to watch that gold and silver melt into the pot… The honey pot 😊
I love honeypots
I was looking at Tomoko's Enterprize channel and saw where he got some silver crystals from you and made a king about 3 years ago and I saw where you started a chess set about 6 years ago. Someone on that channel said it would be neat to see a silver and gold chess set. Still just learning refining, using a torch or a home made furnace, home made vacuum chamber, how to identify the jewelry and everything else. It takes time learning all that and casting the metals is an art. It was nice to see some of your crystals get cast into something.
I began learning to cast using lost-wax. But I lost interest. I’d still like to try it.
I like how at 29:24 when you add the first spoon of SMB and the first gold starts to precipitate, all he ice in the beaker jams up to the top of the liquid.
Have you ever accidentally scrapped a jewelry item that Mrs. Sreetips wanted to save?
considering she buys most of it she probably gets first picks
One time he embedded a diamond into a collectible coin she wanted to preserve. She was not amused.
Shut up… idiot
@@johnschruben3586
I remember the video, mrs sreetips was really upset.
To be fair I'll have to add, that it was just a reproduction of a 20 Dollar gold coin, not a original coin wich would have had numismatic value. If I remember it right, sreetips once mentioned he does not melt or dissolve coins. There is no need to refine them since the issuing county guarantees for the right precious metal content of the coins, so it's a known quantity of precious metals to calculate with.
No. Mr ST wouldn't be here now
I also had an idea....... A Centrifugal separation using a Maytage washing machine, that has a Stainless Steel drum and no agitator in the middle to get in the way.
Waiting for gravity to drop parcipitates is almost unendurable. At my age time is a valuable commodity! What are your thoughts?
Comercial centrifuges can't do large capacity solutions. I figured a way to be able to use 8,1,000 ml beakers at a time, in the drum of the washer. They would be able to pivot as the washer sped up.
Hi. I'm new here and really love your channel. I have a question though, maybe 2. I have a lot of e-waste material like mainboards and old pci cards and old gold painted watches and so on, kilos and kilos. I figured I remove the components that could be of value as they are, such as EPROMs, Coils, Tantalum Caps, Inductors and some ICs. Most of the other components, such as resistors and caps are not worth a lot and I left them on the boards. Now the idea is to break the boards apart so they fit into my plastic container in order to give it a chembath so I can extract all the metals from the boards and the 9k jewlery. From the videos I've seen so far I know that Nitric Acid will break down every metal, except Gold if I just give it enough time and some bublling action or heat it up, please correct me if I'm wrong here, maybe I missed something but as far as my monkey brain understands, Nitric Acid breaks the metals such as Tin, Silver, Copper and Aluminum (or Aluminium) apart. I suspect there could be some other metals on the boards or inside the watches that don't get dissolved in Nitric Acid? Anyways, if I'm correct the Nitric Acid should take out everything that isn't Gold, I would pour the solution into another container for later possible silver extraction (using copper rods). Once I see no more stuff reacting with the Nitric Acid I would prepare 3 parts of Clohidric Acid and 1 part of Nitric Acid in order to obtain the Agua Regia to dissolve whatever gold is left on the boards/jewelry. Bubble action again, or heating it up to make it faster ofc, and transfering the solution into another container until there is no more yellowy reaction going on in my fist container (there should be no gold left then I guess). I would then add sodium metabisulfite to precipitate the gold from the agua regia solution and heat the obtained powder in my table furnace into a blob. Please tell me if the plan is correct and I understood everything correctly, or maybe explain a different, better approach. Could I maybe directly make Agua Regia, extract all metals with it and then just precipitate the gold and toss teh rest? I don't trust ChatGPT and don't wanna blow up my workshop xD. Really looking forward to a professional opinion from someone that does this stuff by the day.
I don't do this by the day, but I think I am pretty knowledgeable about this. Nitric acid will also leave Pt group metals (PGMs) next to the gold. As far as I know, those are pretty rare in computers, so no real need to worry about it, just so you are aware (and don't toss them away). Basically, you are correct.
You will get better results with the first method, but the second method (direct to AR) is quicker, but you will toss silver (and possibly PGMs).
I’ve done trimmed circuit cards fingers by dissolving the base metals out with hot dilute nitric.
Just curious why you continue to use the torch and melt dish method. Why don't you invest in an electric or propane furnace?
Personal preference.
@@sreetips fair nuff 👍🏻
Missed something on inspection! I think what you didn't catch in the melt showed up in the filter! Nice to see the strait forward process for high purity end result!
Have you ever thought about melting metal with a solar death ray? People frame up a lense from an old big screen tv and use it to focus the sun. It might be hard to control but it would save on gas. Also you could do larger amounts, the beam is about an inch wide and will slice through anything.
I’ve seen those videos, melting rocks.
I am new to this. So aqua regia does not dissolve lead and some other basic metals? These are all the black particals in the filter paper?
Aqua regia does dissolve lead (just about anything), but the added sulfuric acid will precipitate lead as lead sulfate (highly insoluble). Besides that, silver will precipitate as silver chloride as that also is insoluble, one of the reasons to remove it with nitric acid before going to AR.
Those black specks were hematite
Thank you
Oh yea! This makes my day complete! Great video. Thank you for sharing.
Afternoon Gunny! Have you ever had issues with the inquartation process? I'm working with some 18K, maybe a bit better. It doesn't seem to want to mix well with the copper I'm using for inquartation. I've melted and stirred it twice now and I'm still getting copper shot in my quenching pot. Any ideas?
That’s normal
Gooooood evening from central Florida! Hope everyone has a great night!
Goooood evening!
I am from Central Florida as well. Nearly 25 years in Orlando now living near Bartow FL.
@@richardhulbert9480 Dade City here... howdy neighbor! 👋😎🌴🌴
QUESTION: If I have been paying attention well enough, could you alternatively take the inquarted gold/silver to your silver cell for extraction of the gold, and then take the gold residue straight from the silver cell feed bag into the aqua regia process for refining (with associated rinses and sulfuric acid lead removal step)? Thank you for all your educational videos.
No, the material going into the silver cell must be relatively high purity to begin with or else the cell will quickly become fouled.
I've been watching your videos for so long now that I can tell from the thumbnail how clean that gold is. Beautiful.
Question for you @sreetips which you may have addressed in a past video. How long could you store the gold in solution after dissolving the gold in aquaregia (spelling?) and boiling off the excess nitric? Can it be store indefinitely or is there a time frame it should be precipitated out?
Forever, as far as I know.
@@sreetips Good to know. Thank you sir for being such a great teacher, my kids and I quite enjoy your video's! My oldest will be starting chemistry soon and is hoping to be able to use the knowledge she has gathered from watching you to bolster what she is going to be learning in school.
That’s fantastic. I was interested in chemistry when I was in school fifty five years ago. Had a small chemistry lab set up in my basement. I took a chem class in high school and got a D. It was too much study and memorizing. I wanted to get down to business and do reactions. My channel is an extension of that. Now that I’m grown up, I can do what I love.
how do you work out the cost of refining the gold and other metals? not so much the buying of jewellery, the flux and acids and materials used while refining?
I don’t know those costs. We buy gold so very cheap at local sales that those costs don’t matter. I wish I could publish some videos on that but Mrs sreetips has asked me not to
It never ceases to amaze me at how much "junk" is left over in some of these steps. Where do you find your gold pieces?
Yard sales and estate sales, mostly. People are clueless about gold and silver. They believe, incorrectly, that paper dollars are more valuable. This misconception creates some fantastic buying opportunities.
@@sreetips That's awesome! How much cash do you think it would take to setup a small refinery operation for a beginner using home-made stands and thrifted wares? Of course I understand there are some pretty hefty premiums for quality glass, but I like the way you've been able to seemingly keep your overhead cost for equipment moderate.
I accumulated it as I needed it. Type lab glassware on eBay. Sometimes you can find a bunch for cheap. The first thing you need before glassware is a fume hood. No way to safely do these reactions without one.
@@sreetips Understood! These are incredibly damaging substances for every part of the body that I'm aware of! Thanks for all your help and thanks for making content of these scientific processes. That SO2 reaction was TO DIE FOR!
Quick question regarding your calculations. Where is the 1.265 for 14K and 0.635 for 10K derived from? If you're inquarting, would it not be simply taking the weight of each Karet multiple it by 25% to get the amount of silver would be needed to lower the Karet for recovery via HNO3?
No, because the karat gold contains silver and base metals that must be accounted for when calculating the amount of silver to add.
@@sreetips I see. Correct me if I am wrong. If I have a 38 gram of 14K bracelet. The gold content of that bracelet can be calculated by part to whole division. 14k/24k equals 0.58 or 58% of pure gold. Then would you inquart 0.145 of silver to knock down the karat?
38g x .583 = 22.15g pure gold times 3 equals 66.45 - (38g - 22.15) = (66.45 - 15.85) = 50.55g x .95 = 48.02g sterling to properly inquart 38g of 14k. Or just multiply 38g time 1.265 = 48.07g sterling to properly inquart 38g of 14k. The last digits are insignificant.
@@sreetips Thank you for taking time out of your day to break the calculations down.
Hello Mr. Sreetips. Silly question here. Can gold somehow be in gas form?
I know it's stupid, but I feel like some of the gold is flying away of the beaker in gas form. Is it possible to place a stannous chloride soaked paper on top of the beaker during the aqua regia process in your next videos to check this?
Thanks.
Yes, there are losses all along the way. Boiling the gold solution will cause finely atomized droplets of gold to exit the beaker and go up the stack.
Beautiful gold. Thanks for your fantastic content.
@29:30 can someone explain why the ice moves up so rapidly?
They freeze to the bottom of the beaker, then release when the solution warms
Can you share details about the respirator/filters you use in which circumstances?
I’m working in a fume hood that draws the harmful gases away from me. I wear a 3MP95 mask when melting metals so I don’t have to breath the smoke.
Can you inquart with gold plated scrap? I've seen you use several base metals to inquart. Using scrap plated material could allow you to recover the gold more easily in the plated stuff and provide the needed base metal.
No, gold plated is junk metals including tin and sometimes lead.
@ 8:00 Darth Sreetips. You gotta admit it's catchy 😆
Sithtips
Thanks for sharing with us Sreetips 🤠 Excellent Work 🐉 God Bless 🙏 I can't wait to get out and do some metal detecting at the lakes here Find some scrap gold.
LOL, for a minute I thought I was hearing Darth Vader doing the melting of the shot 😉 That's a novel approach mr Sreetips 😆
What is the liquid you drop on the test strip to check if there is gold? Thanks.
Stannous chloride testing solution.
Yeah, I have been guilty of getting too excited and jumping the gun. The results are that you end up spending even more time and chemicals redoing. Definitely frustrating.
Is the silver incourtation absolutely necessary for the acids and heat to purify the gold? It won’t chemically react the same I’m assuming? Have you ever tried??
Putting scrap gold directly into Aqua Regia can be done. But it makes a very dirty solution and passivation can occur (hard crust of silver chloride forms and shield the metals from the acids. Both problem are completely eliminated with inquartation.
I never get tired of watching your videos thank you
Have you ever extracted and refined gold from gold ore?
I know there’s several videos on TH-cam be about it. It would be interesting to see your procedure.
I’ve never worked with gold ore. Yield are measured in grams per ton
Hello me again, I have a question i dont think you have ever addressed before. What happens if you have your loaded aqua regia with gold , and just leave it to evaporate ? No MSB or such, just let it air dry out? If i was to guess it would crystallize, but again i,m guessing. Thanks
It can be evaporated to dryness, will form orange chloroauric acid crystals.
@@sreetips interesting? Will it still weigh the same as metallic gold? Thank you for this response, your my go to instructor for alchemy .
Wow this just opened a very new complex set of science for me to look into , thank you Mr Sreetips
Yes, the mass won’t change. A volume of liquid that has gold dissolved in it will weight more than the same volume of liquid with no gold in it.
@@sreetips I still have a long way to go learning how to make monoatomic gold. But i will get there. Cheers
Thank you Sir. Always a pleasure to watch this process.
This is honestly one of the best channels on TH-cam. You should try to make a nice cuban link out of what youve made so far
Dear sir :
Ty for your excellent video ,
I was wondering why u don't use the urea to kil the nitric, what u do instead of using urea?
Thank you for your reply
Incremental nitric dosing; adding just the right amount of nitric to just dissolve the gold. But if I do over-shoot with nitric, then the best method, by far, is evaporation down to a syrupy stage until all the excess nitric has been driven off. Adding urea to kill excess nitric is antiquated and no longer used by modern refiners.
@@sreetips thank u sir for your answer
U are very experienced .with all my respect.
Can I use the white Crystal's of stannous cloride to do the gold test ?
Thanks again for answering.
I use stannous testing solution.
@@sreetips I saw a label on your bottle of the stannous cloride in the video written on it the ingredients of the that cloride but it wasn't readable,
Would you please provide me with that ingredients or how to make a good stannous cloride to test the gold,
That would be very kind of u sir.
QUESTION. I have a vintage class ring, 1944. The inside is stamped “BALFOUR GOLDFLEX”. After watching a boatload of your videos I can tell you know way more than you let on, lol. Do you happen to know ow what goldflex is? Thanks
I’ve never seen “goldflex” but during that time karat gold would be marked 10k. So I’d be suspicious.
@@sreetips thanks for the response. I’ve seen too many conflicting descriptions on the internet. I’ve seen people say it’s nothing, but I’ve also seen some say it’s 8k. It was definite worth asking someone with your kind of experience in the precious metals, though, so thank you. Love watching your refining videos. Keep on keeping on!
Is it safe to pour Nitric acid into a hot beaker after a decantation? I heard that there could be risk of beaker crack when adding cold liquid into hot beaker.
This is what bing copilot says: " For standard laboratory glassware like borosilicate glass, which is designed to withstand thermal stress, a temperature difference of around 100°C (212°F) can still be risky. If the beaker is at 150°C (302°F) and you pour a liquid at 0°C (32°F), the sudden change can cause it to crack."
If there’s liquid in there, I’ve never had a problem. But I did sit a two liter beaker on the heat for just a few minutes dry. When I added some liquid it cracked. So I’d say never add liquid, hot or cold, to a hot dry beaker.
Hello teacher I'm doing the same thing in Korea. These days I have a problem. In winter, the purity was 99.9%, but as the weather warmed up, silver started to show. Teacher you put ice in the video, is this related to Agcl?
I thought you started inquarting with copper and liked that better. What made you go back to silver?
Because I refine silver also. First step is to dissolve the silver, so why not use it to refine the gold. Like refining both metals simultaneously
Hello, just came across your channel. May I ask exaclty what it is that you are doing? Are you taking gold from junk-electronics and refining it? Or are you growing gold in a home lab?
I’m refining the gold from pieces of broken and scrap karat gold jewelry. I buy the scrap gold at local sales, then refine it and my videos. It’s my hobby.
Wow, very impressive! @@sreetips
Could the junk in the filter be lead from the jewelry? Ty SREETIPS for answering us. 👍🤙❤️
Hematite.
What happens if you let the gold laden solution evap all the way? Will the gold be left as a powder ?
You’d end up with burnt orange chloroauric acid crystals. I did this by accident last summer.
Kevin I'm curious, have you ever attempted an AP base metal extraction in lieu of a nitric extraction after inquartation? I would imagine it costing a LOT less in reagents at the cost of a week bubbling outside.
Just a thought for a potential video.
It's how I've done mine (on smaller scales) to save from spending the pretty penny on nitric or making enough to do a batch.
The hydrochloric acid would immediately react with the silver and form a hard crust of silver chloride - passivation.
@@sreetips ya I don't know why I didn't think of that on your end (cause you always work with silver), I always use copper myself for inquartation when needed.
kind of addicted to watching that aqua regia phase and nitric boils cleaning things up... then that ... ok, so I'm hooked !
Where can I buy concentrated nitric acid ?
Amazing that the I've cubes sink to the bottom whole gold in solution nut as soon as you release it the ice cubes fly to the surface
Great work as usual
They were frozen to the bottom of the beaker. The heat from the reaction causes them to release and float to the surface.
What would happen if you added the stump out to the warm solution?
The gold would precipitate.
New to the channel and fascinated with it all.
I’m sure it’s been explained elsewhere, but I’m wondering if you precipitate the silver back out of solution?
Is it difficult? Is it worthwhile? Is it just the cost of doing business when you refine the gold?
Edit: never mind I think I need to check out the silver videos..
He takes the silver waste and either runs it thru a silver cell or cements it out in copper to be refined in a stock pot refining video very little goes to waste on this channel you will enjoy his catalogue of videos for sure look for his silver cell videos they explain the silver recovery I hope you remember to take breaks periodically as u get stuck into the videos
I recover the silver from my silver jar, melt into shot, and run it through my silver cell.
@@sreetips the silver cell videos are on my playlist for the weekend. True alchemy; it’s incredible
what is the orange and yellow fumes at 9:40 ?
Nitrogen dioxide
What were the little white blobs, you pulled out with a tweezer? Just curious. It looked like Borax. I have the same thing occur.
I'm going to melt some 14K and 18K today. Thought I'd try the Copper inquartation you demonstrated.
Those were pieces of plastic that were inside some gold balls.
Wade, make sure and do it in a fume hood. No way to safely do reactions without one.
@sreetips Absolutely! Fume hood is robust! Also a full face respirator, gloves and Flame and Chem resistant lab coat! I watch your tutorials, Gunny. Hard to miss the warnings at the beginning of each one! I'm glad for them and your safety precautions.
I've looked at other sites, occasionally. It is distressing to see some sticking their hands in a beaker with fuming Nitric and not be wearing gloves! YIKES! Also the guys decanting catalytic ceramics. No respirator, no gloves, just sucking in the dust! Unbelievable! I am in the practice of studying each process, researching ect. As well as SREETIPS, the Gold Refining Forum is a solid referencing source. Thanks for that as well! It was your suggestion to me, to become a supporting member.
Your videos are extremely well done and you always give us a heads up, when a potentially energetic reaction will occur. That's why I'm a devoted follower. You do it RIGHT!
Would you concider to use metric numbers in length as well not just only in weights?
When I hear 7 inch, it doesn´t mean anything in Europe.
Thank you Mr Sreetips.
Greetings from Sweden.
Greetings, I’ll do it!
Good afternoon again good sir. Quick question, as always lol. What ratio would you say you use when adding sulfuric acid to precipitate and lead? Or are you just adding a squirt, so to speak? Thank you as always, can never get enough of these videos.
One more question. When inquarting, say you don't have enough gold to make 6k gold (I have some grips for a 1911 I won at auction for 120 bucks that have 20% of their weight being made up of 8k gold and I don't have enough gold to get to 6k)... is there much harm in having a higher ratio of silver to gold?
I add a half a milliliter.
8k gold can be boiled in hot nitric as is. No need to add additional silver to the gold.
@@sreetips Awesome! Added that to the 'recipe' book. Thank you kindly!
@@sreetips I have found that my autism often leads me to not fully communicating all the important information, my apologies for that. I should have noted the 8k gold is 'welded' on top of the silver. It could just be my limited knowledge but I don't see a real option other than melting it all together. It is a very ornate design going across the entire surface so cutting it out isn't an option.
If the 8k gold is welded to a piece of silver, then I’d just boil the whole thing in dilute nitric. The silver will dissolve completely, the 8k gold is low enough gold concentration that the nitric will get all the silver out of the gold too. If you boil it long enough
Are the torches/burners you use oxy-acetylene? Could it all be done using a metal melting furnace? Also, is the burner you use with the ceramic and glassware an induction burner or coil?
The electric burners in my fume hood are cheap electric burners. Oxy/acetylene torch. I’ve used melt furnaces,
Did the hydrochloric acid turn yellow when you first poured it in due to left over nitric acid caught in the gold even after the water boil ?
Yes
Another AMAZING educational efficient video. You r the BEST on tha Tube!!! 💯💯💯
I do have something I hope you can help me out with, I unfortunately do not use Nitric due to cost and availability, what options/substitutes do u recommend inplace of the Nitric boils for refining karat gold? I usually dissolve in acid peroxide bleach, and just tested a new method of Potassium Nitrate and HCL as a Aqua Regia substitute, if I can find a sub for the Nitric boils I'll b SUPER happy.
Thanks in advance, speaking on behalf of your viewers we REALLY appreciate you sharing your knowledge and experience! I can't imagine how many you have educated! You are truly a gift to us! We can not thank you enough! God Bless, I wish u and your family all the best!
I always use nitric acid. Never tried potassium nitrate.
Why does adding ice sometimes put Silver Chloride in the Gold?
Because silver chloride is slightly soluble in hot aqua regia. Adding ice causes it to come out of solution so that it can be filtered out.
What's your ph on the orange disolved hold solution and the clear solution, post precipitation pre rinse? Just wondering how acidic it still is. How much it drops during precip.
Probably pH1 for both
Hello Mrs and Mr Sreetips.
First a clip from you...Then out to use my detectors 🙂
God bless you 🌸🌸
Sreetips ive seen other people use urea to neutralize the acid. Does that take away from the final weight by using that?
Urea isn’t used by modern refiners. Evaporation is a far superior method to remove excess nitric.
Sreetips: Regarding Sterling silver, if it is 88-90% silver, what price per ounce, as a percent of spot, would you pay for silverware and still consider it to be a good deal? Also, when appraising silverware, what would you deduct for components that are not sterling, like knife blades? Thanks!
80% of spot. I figure 10g of sterling for the weight of the handle. But if you end up paying 100% it’s still a good deal because silver is grossly undervalued.
The Ring doorbell sound made my dog bark!
Also, if your stannous tests smoke yellow, its because of excess nitric correct? Thats what i believed anyway, i added a lot of SMB (to avoid Urea), and my 1st drop had gray/brown crystals with gold mud inside rhem and beside them. Luckily hot water fixed it all in the end, but thats the 2nd time in hundreds of runs over years that i had those crystals, first time a decade ago, they were green/yellow crystals. This time, I just remember my stannous test smoking yelleow, and having to add a whole lot of SMB before any color change or gold drop. It was a scary moment that still has me puzzled 5 days later.
I tell myself it was to much nitric (im usually using Sodium Nitrate), and then to much SMB to neutralize it. But im honestly unsure. Good news is you rarely, or likely never lose the gold in solution forever. But sometimes you must worker 10x harder to get the gold back because you made a mistake. And that day i made some mistake. But the fix was easy, fortunately for me.
I use evaporation to drive off excess nitric. It’s far superior than adding reagents to kill excess nitric. It’s easy to do, it works every time, just takes a little longer.
My question is that blowout can it be added to the current batch or not? if not why?
What blowout? Not sure what you’re asking.
I'm getting a yellow precipitate coming Ng from my gold while dissolving in the aqua regia. Do you have an idea as to what this is? Does it contain any gold?
Probably silver chloride. I just filter it out, pass it through the same filter a second time if it’s still cloudy. Then I add the filter to my paper storage for later processing.
Do you use Distilled water for the ice cubes in this video?
Tap water
I have to say that I consider your videos better than any other and I recomend to my friends and family that they watch your videos.
Thank you!
Awesome as always just wondering if you would maybe do a show on refining iridium from old pool cell chlorine generators?????
I don’t have a clue on how to refine iridium.
I was thinking it might be similar to the way they get it from spark plugs. I was just curious cause I’m in the pool and Spa business and we throw away hundreds of these cells every year thank you sir.
Refining platinum group metals requires a lot more chemistry and highly specialized equipment. Gold and silver are like a cookie recipe compared to PGMs. Not suitable for a hobby refiner to risk it.
Another great video, keep up the good work sir.
19:40 Could those be lead balls that precipitated out from the sulfuric acid?
Hematite
Just wondering, why don't you ever use silver shot for inquarting?
It’s not recommended - palladium follows the silver and could build up.
@@sreetips
Thx.
I dig how ya monogram EVERYTHING, I have a looooong name, having caught the names of 3 U.S Generals..
So "NOT YOURES" in sharpie on all my tools/items will usually suffice ...
And if cans/bottles full of un-labeled chemical/organic solvent: "NOT BOOZE"
And if within $pendy bottle of Tequila: "NOT YOURE BOOZE"...;)
I really DIG watchin ya work away in youre own personal Alembic. Its truly fascinating stuff. Ive picked up quite a bit from yee, even though Im not in the precious metals game whatsoever (Aside from firearms/Hand-loading ammo I suppose?..;)
For the decade plus I've been watching, the first spoonful of SMB is always my favorite reaction 👌🏻
Would you be interested in refining a bunch of gold off antique china dishware
Unfortunately I don’t offer any refining services.
Amazing how fast the copper goes into solution!
Does stompout change the PH? Does it neutralize the acid?
Maybe a little, but I’ve never measured it. My guess is that it’s pH1 before and after precipitation.
Why do high end beakers not shatter because of thermal shock?
Borosilicate glass
But they’re not bullet proof. I put one on the heat for about a minute dry. When I added some water the beaker cracked.
what filter paper do you use?
Whatman number two medium flow
Ahh man been waiting for a new show lol, great vid
Can i ask what size buechner funnel you use?
I use 11cm in this video
I think silver inquarted gold is one of the most beautiful metals. i want a to plate my 1911 with it instead of nickel. (it looks alot like nickel)
It has a certain luster that’s very appealing.
Back to the yeller stuff. Love the colors of both the blue and red/yellow and then to the bright yellow.
Last two nitric boils could have been saved to reuse. $ wasted...
You got us….” To be continued….” Good video, keep up the great work
The paper squares are a good reference for size 0.5cm²
Excuse My ignorance, so allá these si refining, same as "growing silver cristals" you are not creating artificially the environment so the silver or gold can "grow" it's a refinament technique where You end up with les matireal but more puré, rigth ? You don't start with 200 grms and end up with a 1,3 kilos of silver. Please correct me, i want to learn.
I refine gold. I use sterling silver, that I buy at estate sales, to refine the scrap gold. I recover the silver from that, melt into shot, and run it through my silver cell. Silver is a by-product of my gold refining. The cell converts the impure silver (about 980 parts per thousand silver) to high purity four nines fine (9999 parts per ten thousand) pure elemental silver metal. So I’m refining the impure silver, into high purity silver, not creating silver out of thin air. When it’s full, I harvest the pure silver crystal, put it away and forget about it. Then I repeat the whole thing again.
Never get tired of watching that gold drop out of solution.
30:59
Thank you for your informative and thorough content! Can you point me to books or websites that have written directions on refining karat gold into “pure” gold?
Thanks again.
Try the goldrefiningforum.com
@@sreetips
Thank you sir.
Just looking at this man work you know its more for fun than for profit hehe. Good on ya, great men content!
Ran the numbers for those who are thinking of bidding on the bracelets. The melt value of the Charleston bracelet is about $450, and the melt value of the San Marco is a bit over $460. Don't low-ball the senior chief!