Sreetips, in the beginning the solution was evaporated too far - past the point of supersaturation. This is why from that point we see ribbons of metallic gold fighting to stay in solution, and the sparkles and flakes later on. In the end you’re not losing anything other than that gold that got caught in the filter paper.
Mr. Sreetips my 16y.o. son gave the best compliment you can get from a modern teen. "Hey dad, that's actually really interesting..." & he honestly meant it!
Yep at age 16 I certainly agree sir. Definitely keep that one close and softly but determined give him the the quality rules of life. Be strong be proud do your best we all make mistakes but as long as we learn from them. Life can be beautiful. Especially love your family unconditionally! Because as we all know , when shit hits the fan in a big way. It’s always family that will be there from the beginning to the end 👍🇦🇺❤️
it must be super saturated causing that effect.. When solvents are heated they have a higher carry capacity & when they cool down they precipitate.. 2:00 what an awesome visual of the gold... you can see the covalent bond pulling mass together coupled with super saturation & cooling
my theory of why gold was coming out after you evap it down to drive the nitric is, as you evap the nitric you also drive off some HC and only so much gold can be held by the solution per ml so as the nitric and HC gets evapped gold has no choice but to come out cause it has nothing to hold it. Kind of like how the air can only hold so much moisture and when it reaches saturation the moisture drops as rain/snow.
Your commentary ads a lot to the entertainment value of your videos. You make this interesting in every way. I never thought that anticipation for the next part would be so suspenseful 😂
Talk about being on the edge of your seat, when it started foaming I was right there with you saying no don't do that! Man the stratification of the concentrate and HCL was fascinating to see, have a good one sir!
You never fail to entertain with your videos. The last monster series and now this one have been a joy to watch. Looking forward to the melt and pour, the last one had me on the edge of my seat. You must have nerves of steel, or gold maybe. Thanks for sharing your work with us.
Redox!! You got things so concentrated that the H2AuCl4 underwent auto redox to 2HCl + Au(s) + Cl2(g) -- a source of the frantic bubbling even after it had cooled down. So Cool!! It's a tribute to your Chemical skill that the ceiling of your fume hood, seen in the previous video, is so clean...
Well that was just fascinating. Another example of the complex nanoparticle makeup of chloroauric acid solutions. As already mentioned you supersaturated the solution and it wanted to spit out nanoparticle gold as well as crystalline metal. That accounts for the intense colours which are a result of the Rayleigh scattering of light and a reason why modern medicine uses gold as a very sensitive indicator based on its weird optical properties. It appears you also forced it into gold(iii)chloride and possibly gold oxychloride + gold(iii)oxide when you added the peroxide. Those compounds don't like to hang together but the high concentration forces them to crash out of the solution. They're fairly unstable but they all have interesting optical properties due to the gold. Loved seeing microscopic gold rain in the beaker! Outstanding and without losing any gold either (except the tiny amount in the filter paper.). No contamination by the look of it at all.
I guess there's no way to avoid it. Everyone I've watched that makes it big on TH-cam at some point goes from making videos of what they are doing to doing things for a video. When that happens they learn all kinds of tricks to maximize earnings, such as making shorter videos or bigger batches. And I guess it's the way of things, but it makes me sad every time and it feels like the end of something good. That said, I've really enjoyed your videos and your calm demeanor and methodical ways. I do hope you are successful in what your trying to do now, and that you squese every last penny out of YT. I don't think you have to much time left before things start to change, so make a race out of it. love from Norway, Shalom !
@@sreetips If you serve through it, then perhaps it now is a job. But if you are only increasing your wealth, maybe even unnecessarily so, then perhaps you should retire. Ask God and He will guide you as He sees fit, for a greater purpose. Greater than both of us probably 😊
Good advice. I find myself worshipping wealth instead of Him. The world (the Devil) has a way of pulling you in and away from the spirit. And he uses GOLD to do it.
At the near boil over I was starting to think you were on the verge of having to pause the video to change drawers lol Your videos are always facsinating to watch thanks for sharing👍
I think we’re seeing a very good demonstration of saturation. The HCl can only hold so much gold. It’s lighter than the much denser liquid below so it stratifies. As you add more HCl the upper layer gets larger and the bottom layer gets smaller. I’m only at 5:38 as I write this. My guess is that when it’s all done you’ll have about the same volume you had before you began your denox reduction.
Not only immicible, but your concentrated solution was super saturated. Gold was falling in and out on the convective currents. When you added cold HCl, it created a site of nucleation at the interface of hot and concentrated and cold and free of solute. Very very cool
im thinking supersaturated mixture causing the gold to crash out when disturbed...no knowledge of refining and only basic chem understanding but just a thought
Hello Mr. Sreetips! Love seeing your work and your method. The results are always spectacular! I have a tip for washing out beakers and such: use a spray bottle, it breaks the surface tension in pretty much the entire beaker and washes them good without awkward wrist movements!
That solution got super saturated after the nitric acid boil-off, that's why the gold precipitated out of it, specially when you rehydrated it with cold hydrochloric acid.
When added HCl to the syrup, you've actually salted out the chloroauric acid from the saturated soln. Also, all the HNO3 should've been evap completely after soln reached >122° C (the boiling temp of azeotropic 68% HNO3 / 32% H2O is 121°) The same for HCl is 108°C at 20% conc azeotrope, beyond that temp no free HCl should be in soln. And no excess HCl means the chloroauric acid will decompose, especially at elevated temp. You should have some excess of HCl to shift the equilibrium. After gold is reduced, more oxidizer is needed to put it back to soln
I'd assume that some of the gold chloride crystalized as the solution evaporated and became over saturated, which then decomposed to metallic gold due to excessive heat. Evaporation should always be done at low heat and never boiling. This is your major mistake, Sreetips. Boiling should only be used for rinsing and never for dissolving or evaporating.
Hey, Love this one sreetips! Maybe a word of caution. Your supersaturated solution is very hot, above the boiling point of water. I am no expert, but it might be possible to cause a steam explosion (yes maybe small) that could spew your extremely valuable solution around. But, it may be that the density of the Auric chloride keeps the water on top. Beautiful work BTW.
Hydrating with HCl while driving off the nitric, and keeping the volume no less than half your original HCl volume, should achieve the same result as reducing to syrup if you drive all the fumes off. With the benefit of no super saturated solution and gold crashing out.
I see many commented with the same thought i had. Not enough liquid to keep that much gold in solution. Might have just put in some nitric & reformed aqua regia. Almost lookslike your gonna have to do it all over again. Ty for taking us along
This is better than watching a magician, because this is all real. Physics on display in some rarely seen procedures. That gold precipitate early in the video looked like a swarm of mermaids in the ocean. There is a degree of art to refining, so many unexpected results over the years. This is top top tier content.
The problem is that it would likely precipitate some of the contamination from the original 995 bar as well. Perhaps filtering prior to evap would take care of some of it, but I doubt it would be as efficient. Plus you'd need to factor in the energy cost of heating the solution compared to SMB or gas generator.
There's no contamination. That layer is set up from water, from the melting ice, being far less dense than your chloroauric acid. Your best bet was to using your magnetic stir bar to keep the solution, with ice, circulating while you add your SMB. It'd have allowed you to add your SMB at a small and steady rate with out the big -risky- fizz up.
Sreetips, It's pretty similar to what happened when you heated it to dryness: the chloroauric acid crashes out because of oversaturation. However, it doesn't like to be in its solid form and would likely be shedding chlorine or HCL gas to precipitate out the elemental gold. The science of supersaturation is a bit weird, though -- at least it's not possible to actually lose any of your gold this way :)
Cant Wait for the pour dude, Id be shaking :) Good luck with it and thanks for letting us take part in your journey and a Happy New Year to you Sreetips and family.
I've often wondered how the term Aqua Regia came about. Did they get tired of saying "its a 3 to 1 mixture of hydrochloric acid and nitric acid." and "We've got to call it something COOL!" lol... Thanks for your vids and channel. Talk about a mesmerizing experience seeing that Gold shine.
Mr Sreetips you got some serious guts refining 24 ounces of Gold … the glass beaker company must award you to have so much trust in those glass beakers …. Love and respect from India
Mr sreetips im a new subscriber love the content, keep them coming, been very educational and enjoyable could I ask if we could get a transcript in your videos with a list of chemicals used and there concentrations just as an easy reference to what you use
I think this solution needs 2 Sulfuric gas refinements...Not only was the Nitric driven off but the syrup had a little too much HCL driven off also...But with 2 SO2 refinements, that'll be the purest .9999 49.7 oz Ag bar in history!!
i agree. after boiling away the nitric it wasn't oquaregia anylonger and when you added hydroclric the gold couldn't stay in solution and started coming out. there was just to much gold in solution. i'm no chemist it just stands to reason.
9:38 What would happen if you let it reduce and evaporate to zero liquid at room temp? Would all the gold still be there or would some have evaporated?
Chloroauric acid is not stable at high temperatures: with prolonged boiling it will decompose to gold, hydrochloric acid, and chlorine. I made a solid sample of chloroauric acid for fun a few years ago, and this was an issue I ran into repeatedly then. The only way to obtain solid HAuCl4 is evaporation under vacuum followed by drying over KOH.
@@sreetips Your experience matches mine: its not too difficult to get some HAuCl4 to crystallize out. However, getting a completely dry sample is much more difficult. The crystals you got look much nicer than mine (I let the syrup dry out over NaOH for a few months-- it turned to a brick when I came back to it)
Feel like sulfamic acid would be better than evaporating down to a super concentrated solution to neutralize the nitric since once it cools that gold drops out of solution
Hey streetips got a question? What would happen if you just boiled the solution till it was a slug or dry powder. Could you heat it up and melt it into gold? What im trying to say is could you skip the stump out step? Thanks love your vidios
Evaporating to dryness, then trying to melt the crystals into metallic gold. I’ve never tried it, but my guess is that the gold would go up in purple smoke.
Now I know this may be a stupid question because I'm not at all familiar with chemistry. Is gold in solution as heavy as solid gold or the same as water? This is the only channel I watch in regards to chemistry and I can't seem to get enough of it. You may get a laugh out of my question but I have always wondered since watching sreetips. Thanks
Well that was fun! 🤣 I kept thinking your heart must be racing a mile a minute. I wonder if you could have used that gas infusion to precipitate it out? I can almost hear you as the color change occurred! 🤔
Hello I’m new to this and was wondering ?? I don’t have to many components and I wanted the bacily put everything into nitric acid first to remove the maximum amount of silver before I try to remove the gold, will this effect the gold for example I know it won’t be a problem for Ic chips but if I have exposed gold like on boards would the nitric acid take the gold or am I safe just to do a nitric bath first on everything, the reason I ask as I have limited resources and can’t afford to do everything separately
Syrup, while a chemist might say, we have this Supersaturated gold salt solution, we add some hydrochloric to get it just fully saturated 10:15 I guess the boil of nitric was so efficienr it broke some of the salts into some other salt which is why you needed to rehydrate with H2O2.
I don't know what the difference is between this solution and the one you made with the 24oz bar, but this seems much more brown. The other solution was an insane orange color that was almost glowing. Then you really evaporated this to a crazy concentration. It was cool to see, but kind of scary. I hope all goes well in part 3.
It's so interesting to see what difference a change in scale produces. It was so weird to see that syrup re-hydration have that reaction with the gold coming out of solution like that. I'm stabbing in the dark here, but is it possible that this amount of gold has added sufficiently large amounts of gold isotopes to cause this reaction to differ from previous smaller scale purifications?
Once again, Sreetips is using too much heat here. You should always evaporate a solution on low heat and not boiling. The solution became over saturated, causing some gold chloride to crystallize and then decompose to metallic gold due to the excessive heat.
*@**6:32**: By boiling your Agua-Regia solution down (Too Much ????) you have changed the PH Levels, thus causing some of the dissolved Gold to precipitate out of solution because the density of your brew is now so low that the Gold has nowhere to go.*
Hot solutions can hold more than cold solutions, like when we were kids we made those rock candy sticks with sugar water that we supersaturated with sugar and when it cooled off the sugar would condense on the stick.
It's absolutely incredible, I'm not sure anybody's documented f****** around with huge amounts of gold before and just seeing what happens, this is amazing research honestly.
Tune in tomorrow for the exciting conclusion. Will our lab coat hero pour a perfect bar? Will he perform another purification and S0² precipitation? Same Sreet Time Same Sreet channel
I believe you fully saturated the solution when you boiled it down and crashed gold out of solution by over boiling to a syrup. I recommend figuring out the amount of liquid you will need to keep the gold from crashing out for future experiments. 👍 I always love your vids though, no matter what. Especially when Mrs Sreetips gets involved. 😁
Oh... And you should have added a healthy muriatic dose and then restarted the nitric trickle... Reform aqua regia to re-dissolve the gold. ... For future reference. 🤘
You mention possible contamination. Was the ice distilled water or tap? Maybe one of your other ingredient? How “pure” is your acids or you stump out? Is it possible they had trace contaminates?
Tap water. I think there was some platinum group metals in that gold bar. That would explain the weird layering during the re-hydration and the layering during the precipitation.
That watch is a fine example of the importance of working under a laminar flow hood. Even working outdoors can be dangerous. Yet working indoors without proper ventilation is a slow death wish.
That is terrifying when the unexpected happens during a refining. I just had a disaster happen with a 3 ounce refining where some of the karate stamps where not accurate so I over inquarted. It crumbled and some of it even settled as the purple colloidal gold. My refining turned into a recovery process. Still working on it!
... p.s.: forgot this... I recommend to stir the solution while precipitate the gokd with SMB. It would take to long to explain, but believe me you will need much less SMB. And its good to save in times like these
I'm not sure.. just thinking a bit. When you dissolve larger batches of Gold it's obvious your concentration of salts increases judging by the colour of your solutions. I think when you percipitate then probably more PGM's percipitate with the Gold.
Yeah I also had the impression this solution was also more red than the orange we are used to of ChloroAuricacid @@sreetips The solution?: Just dilute before percipitation with 4 liters of Distilled water and split the batch up to be safe for boil overs? I see Asian refiners always dilute their solution before percipitation of Gold.
Another amazing video thank you for showing us these things also on top of that is that 52 oz bar of gold going to be a giveaway LOL I know better than that just a joke sir I hope everything continues to be well for you and your family and happy New Year's to you
Probably a stupid question. When you said there might be contaminates. The ice cubes you were using. Were they from distilled water? Would that mean the difference? I don't know. Just wondering. Enjoy your video's. Thanks again. 😎👍🇨🇦
Sreetips, in the beginning the solution was evaporated too far - past the point of supersaturation. This is why from that point we see ribbons of metallic gold fighting to stay in solution, and the sparkles and flakes later on. In the end you’re not losing anything other than that gold that got caught in the filter paper.
Mr. Sreetips my 16y.o. son gave the best compliment you can get from a modern teen. "Hey dad, that's actually really interesting..." & he honestly meant it!
You're teaching him right.
@darrellsmith5395 Much appreciated... I'm trying my best.
If i learned chemistry this way i would have been paying serious attention haha
Wish I had someone show me this stuff when I was 16. Well done sir. 💪🫡
Yep at age 16 I certainly agree sir. Definitely keep that one close and softly but determined give him the the quality rules of life. Be strong be proud do your best we all make mistakes but as long as we learn from them. Life can be beautiful. Especially love your family unconditionally! Because as we all know , when shit hits the fan in a big way. It’s always family that will be there from the beginning to the end 👍🇦🇺❤️
it must be super saturated causing that effect.. When solvents are heated they have a higher carry capacity & when they cool down they precipitate..
2:00 what an awesome visual of the gold... you can see the covalent bond pulling mass together coupled with super saturation & cooling
I just wanted to add the theraputic qualities of your videos, so soothing
Thank you for making monster bars lately. Us subscribers really appreciate it! I have the flu right now and TH-cam is getting me thru it.
my theory of why gold was coming out after you evap it down to drive the nitric is, as you evap the nitric you also drive off some HC and only so much gold can be held by the solution per ml so as the nitric and HC gets evapped gold has no choice but to come out cause it has nothing to hold it. Kind of like how the air can only hold so much moisture and when it reaches saturation the moisture drops as rain/snow.
Saturation is the term hehe
Yeah, def want more HCl when evaporating down that far, preferably before it drops out of solution.
That's what happens.
It doesn’t work in that way
I'm glad you mentioned it. I was thinking the exact same thing. It has happened before only when the concentration was far less.
Your commentary ads a lot to the entertainment value of your videos. You make this interesting in every way. I never thought that anticipation for the next part would be so suspenseful 😂
Beautiful color and effect, was holding my breath when you were adding the SMB during the foam reaction. Nice work Sreetips.
Talk about being on the edge of your seat, when it started foaming I was right there with you saying no don't do that! Man the stratification of the concentrate and HCL was fascinating to see, have a good one sir!
By far the most beautiful and intriguing reactions you've done yet. And the resulting Crystaline gold was jaw dropping. Good form, laddy!
You never fail to entertain with your videos. The last monster series and now this one have been a joy to watch. Looking forward to the melt and pour, the last one had me on the edge of my seat. You must have nerves of steel, or gold maybe. Thanks for sharing your work with us.
Hello Mrs and Mr sreetips.
Thank you Sir. Great clip as always.
God bles , and take care.
Arne
MEGA MONSTER SCIENCE!!! this is by far my favorite series from you. just incredible
Redox!! You got things so concentrated that the H2AuCl4 underwent auto redox to 2HCl + Au(s) + Cl2(g) -- a source of the frantic bubbling even after it had cooled down. So Cool!! It's a tribute to your Chemical skill that the ceiling of your fume hood, seen in the previous video, is so clean...
Most amazing 50 plus bar I've ever seen. Congratulations
This video had me on the edge of my seat Senior!
Well that was just fascinating. Another example of the complex nanoparticle makeup of chloroauric acid solutions. As already mentioned you supersaturated the solution and it wanted to spit out nanoparticle gold as well as crystalline metal. That accounts for the intense colours which are a result of the Rayleigh scattering of light and a reason why modern medicine uses gold as a very sensitive indicator based on its weird optical properties.
It appears you also forced it into gold(iii)chloride and possibly gold oxychloride + gold(iii)oxide when you added the peroxide. Those compounds don't like to hang together but the high concentration forces them to crash out of the solution. They're fairly unstable but they all have interesting optical properties due to the gold. Loved seeing microscopic gold rain in the beaker! Outstanding and without losing any gold either (except the tiny amount in the filter paper.). No contamination by the look of it at all.
I guess there's no way to avoid it. Everyone I've watched that makes it big on TH-cam at some point goes from making videos of what they are doing to doing things for a video. When that happens they learn all kinds of tricks to maximize earnings, such as making shorter videos or bigger batches. And I guess it's the way of things, but it makes me sad every time and it feels like the end of something good.
That said, I've really enjoyed your videos and your calm demeanor and methodical ways. I do hope you are successful in what your trying to do now, and that you squese every last penny out of YT. I don't think you have to much time left before things start to change, so make a race out of it.
love from Norway, Shalom !
I feel the same way. My wonderful hobby now feels like a job. I may retire soon. Feels like work.
@@sreetips If you serve through it, then perhaps it now is a job. But if you are only increasing your wealth, maybe even unnecessarily so, then perhaps you should retire. Ask God and He will guide you as He sees fit, for a greater purpose. Greater than both of us probably 😊
Good advice. I find myself worshipping wealth instead of Him. The world (the Devil) has a way of pulling you in and away from the spirit. And he uses GOLD to do it.
At the near boil over I was starting to think you were on the verge of having to pause the video to change drawers lol
Your videos are always facsinating to watch thanks for sharing👍
I almost had to change mine! lol
lol
This community has a great sense of humor
Really enjoy watching your videos I’m a welder and a coin collector. Thank you for your service Sir
Thank you
I think we’re seeing a very good demonstration of saturation. The HCl can only hold so much gold. It’s lighter than the much denser liquid below so it stratifies. As you add more HCl the upper layer gets larger and the bottom layer gets smaller. I’m only at 5:38 as I write this. My guess is that when it’s all done you’ll have about the same volume you had before you began your denox reduction.
You are welcome. Demonstrably entertaining! With a couple of “edge of my seat” moments knowing what’s at stake. Thank you Sir!👍👍🤟
Wow, those layers in the evaporated solution and the ribbons of gold crystals coming out of solution looked amazing. Fascinating video ❤
Awesome! Can't wait to see the results of the 50 ounce bar of gold. Never fails to amuse me!
Not only immicible, but your concentrated solution was super saturated. Gold was falling in and out on the convective currents. When you added cold HCl, it created a site of nucleation at the interface of hot and concentrated and cold and free of solute. Very very cool
im thinking supersaturated mixture causing the gold to crash out when disturbed...no knowledge of refining and only basic chem understanding but just a thought
I think the bar had some PGMs.
@@sreetipsooo yeh thats a great thought! Either way keep up the great content. I always enjoy watching and learning from your videos
Hello Mr. Sreetips!
Love seeing your work and your method. The results are always spectacular!
I have a tip for washing out beakers and such: use a spray bottle, it breaks the surface tension in pretty much the entire beaker and washes them good without awkward wrist movements!
You had 2" first timers" in one episode. Frankly. It was my first time too😂
Fantastic outcome so far.
Thank you for taking the time to make these videos Thank you❤ I have wanted to learn how to do this SAFELY You are very awesome
great videos . have learned a lot. good work.
That solution got super saturated after the nitric acid boil-off, that's why the gold precipitated out of it, specially when you rehydrated it with cold hydrochloric acid.
I’d expect it’s crystals of chloroauric acid.
@@chemistryofquestionablequa6252 If it were chloroauric acid crystals, they would dissolve after more HCl was added.
@@chemistryofquestionablequa6252yeah - i think thats what my man is saying
I suspect PGMs.
Correct, with a few particles of metallic gold. But not a bunch as seen here. Theres something else amiss.
When added HCl to the syrup, you've actually salted out the chloroauric acid from the saturated soln.
Also, all the HNO3 should've been evap completely after soln reached >122° C (the boiling temp of azeotropic 68% HNO3 / 32% H2O is 121°)
The same for HCl is 108°C at 20% conc azeotrope, beyond that temp no free HCl should be in soln.
And no excess HCl means the chloroauric acid will decompose, especially at elevated temp. You should have some excess of HCl to shift the equilibrium.
After gold is reduced, more oxidizer is needed to put it back to soln
I'd assume that some of the gold chloride crystalized as the solution evaporated and became over saturated, which then decomposed to metallic gold due to excessive heat. Evaporation should always be done at low heat and never boiling. This is your major mistake, Sreetips. Boiling should only be used for rinsing and never for dissolving or evaporating.
16:20 he is adding sugar to the forbidden iced tea
Hey, Love this one sreetips! Maybe a word of caution. Your supersaturated solution is very hot, above the boiling point of water. I am no expert, but it might be possible to cause a steam explosion (yes maybe small) that could spew your extremely valuable solution around. But, it may be that the density of the Auric chloride keeps the water on top. Beautiful work BTW.
Absolutely, moving slow with this is highly advisable.
Hydrating with HCl while driving off the nitric, and keeping the volume no less than half your original HCl volume, should achieve the same result as reducing to syrup if you drive all the fumes off. With the benefit of no super saturated solution and gold crashing out.
Well done sir this was a very interesting drop I'm looking forward to seeing how this bar looks in the end thank you for sharing this six stars
I see many commented with the same thought i had. Not enough liquid to keep that much gold in solution. Might have just put in some nitric & reformed aqua regia. Almost lookslike your gonna have to do it all over again. Ty for taking us along
This is better than watching a magician, because this is all real. Physics on display in some rarely seen procedures. That gold precipitate early in the video looked like a swarm of mermaids in the ocean. There is a degree of art to refining, so many unexpected results over the years. This is top top tier content.
Oh Lord, what have we done??? L0L. Never a dull moment watching you playing with precious metals. Cool stuff Sreetips...
I'm wondering if the precipitation seen @6:00 and onward can be developed into a way to precipitate the gold on a larger scale.
The problem is that it would likely precipitate some of the contamination from the original 995 bar as well. Perhaps filtering prior to evap would take care of some of it, but I doubt it would be as efficient. Plus you'd need to factor in the energy cost of heating the solution compared to SMB or gas generator.
There's no contamination. That layer is set up from water, from the melting ice, being far less dense than your chloroauric acid. Your best bet was to using your magnetic stir bar to keep the solution, with ice, circulating while you add your SMB. It'd have allowed you to add your SMB at a small and steady rate with out the big -risky- fizz up.
so fun going along with sreetips on this journey.
Thank you for doing these videos
Sreetips, It's pretty similar to what happened when you heated it to dryness: the chloroauric acid crashes out because of oversaturation. However, it doesn't like to be in its solid form and would likely be shedding chlorine or HCL gas to precipitate out the elemental gold. The science of supersaturation is a bit weird, though -- at least it's not possible to actually lose any of your gold this way :)
Wow heaps of stump killer but that is going along just dandy. See you in PT3.👍🇦🇺
“Imbecile” 😂 that made me laugh 🤣
Cant Wait for the pour dude, Id be shaking :) Good luck with it and thanks for letting us take part in your journey and a Happy New Year to you Sreetips and family.
I've often wondered how the term Aqua Regia came about. Did they get tired of saying "its a 3 to 1 mixture of hydrochloric acid and nitric acid." and "We've got to call it something COOL!" lol... Thanks for your vids and channel. Talk about a mesmerizing experience seeing that Gold shine.
Happy New Year Sreetips!
Happy New Year!
Mr Sreetips you got some serious guts refining 24 ounces of Gold … the glass beaker company must award you to have so much trust in those glass beakers …. Love and respect from India
It is a little nerve racking have that much gold in a glass container. Metal and glass are not a good combination.
Always great content thank you, what's the name of the book you have mentioned in the past where you learned all this.
Refining Precious Metal wastes
Looking good sreetips, great job 👍
Mr sreetips im a new subscriber love the content, keep them coming, been very educational and enjoyable could I ask if we could get a transcript in your videos with a list of chemicals used and there concentrations just as an easy reference to what you use
I think this solution needs 2 Sulfuric gas refinements...Not only was the Nitric driven off but the syrup had a little too much HCL driven off also...But with 2 SO2 refinements, that'll be the purest .9999 49.7 oz Ag bar in history!!
Great show, can't wait.
Great videos by the way, I watch you all the time. This part about gold really interests me
You are a brave man! I would be scared to death handling that quantity at once. Bravo!
i agree. after boiling away the nitric it wasn't oquaregia anylonger and when you added hydroclric the gold couldn't stay in solution and started coming out. there was just to much gold in solution. i'm no chemist it just stands to reason.
9:38 What would happen if you let it reduce and evaporate to zero liquid at room temp? Would all the gold still be there or would some have evaporated?
It would still be there.
Chloroauric acid is not stable at high temperatures: with prolonged boiling it will decompose to gold, hydrochloric acid, and chlorine. I made a solid sample of chloroauric acid for fun a few years ago, and this was an issue I ran into repeatedly then. The only way to obtain solid HAuCl4 is evaporation under vacuum followed by drying over KOH.
I made some by mistake once. But I can’t remember how I did it.
It was jewelers tool drawer sweeps about 5 months ago.
@@sreetips Your experience matches mine: its not too difficult to get some HAuCl4 to crystallize out. However, getting a completely dry sample is much more difficult. The crystals you got look much nicer than mine (I let the syrup dry out over NaOH for a few months-- it turned to a brick when I came back to it)
Feel like sulfamic acid would be better than evaporating down to a super concentrated solution to neutralize the nitric since once it cools that gold drops out of solution
Hey streetips got a question?
What would happen if you just boiled the solution till it was a slug or dry powder. Could you heat it up and melt it into gold?
What im trying to say is could you skip the stump out step?
Thanks love your vidios
The acid would just crystalize. en.wikipedia.org/wiki/Chloroauric_acid#/media/File:Chloroauric_acid.jpg
Evaporating to dryness, then trying to melt the crystals into metallic gold. I’ve never tried it, but my guess is that the gold would go up in purple smoke.
Now I know this may be a stupid question because I'm not at all familiar with chemistry. Is gold in solution as heavy as solid gold or the same as water?
This is the only channel I watch in regards to chemistry and I can't seem to get enough of it. You may get a laugh out of my question but I have always wondered since watching sreetips. Thanks
A solution that contains dissolved gold will be much heavier than the same volume of liquid with no gold.
@@sreetips Law of conservation of mass.
Can you do a video on the equipment/supplies you used and where to buy it
I bought all my glassware on eBay.
I wonder if that initial surface precipitate was gold coming out of a super saturated solution
Well that was fun! 🤣 I kept thinking your heart must be racing a mile a minute. I wonder if you could have used that gas infusion to precipitate it out? I can almost hear you as the color change occurred! 🤔
Intriguing reactions! Wow I could feel the stress too! So fun
Goooood evening from central Florida! Hope everyone has a great night!
Goooood evening!
6:13 that would make a pretty snow globe
its so pretty, its everywhere , better get to it NOW ,hell mabe im worng
Hello I’m new to this and was wondering ?? I don’t have to many components and I wanted the bacily put everything into nitric acid first to remove the maximum amount of silver before I try to remove the gold, will this effect the gold for example I know it won’t be a problem for Ic chips but if I have exposed gold like on boards would the nitric acid take the gold or am I safe just to do a nitric bath first on everything, the reason I ask as I have limited resources and can’t afford to do everything separately
Nitric does not dissolve gold.
Syrup, while a chemist might say, we have this Supersaturated gold salt solution, we add some hydrochloric to get it just fully saturated 10:15
I guess the boil of nitric was so efficienr it broke some of the salts into some other salt which is why you needed to rehydrate with H2O2.
I don't know what the difference is between this solution and the one you made with the 24oz bar, but this seems much more brown. The other solution was an insane orange color that was almost glowing. Then you really evaporated this to a crazy concentration. It was cool to see, but kind of scary. I hope all goes well in part 3.
It's so interesting to see what difference a change in scale produces. It was so weird to see that syrup re-hydration have that reaction with the gold coming out of solution like that. I'm stabbing in the dark here, but is it possible that this amount of gold has added sufficiently large amounts of gold isotopes to cause this reaction to differ from previous smaller scale purifications?
Once again, Sreetips is using too much heat here. You should always evaporate a solution on low heat and not boiling. The solution became over saturated, causing some gold chloride to crystallize and then decompose to metallic gold due to the excessive heat.
Mr Sreetips. You know a lot more than you make out. You are far more accomplished than an amateur hobbyist. You are just very modest.
11:00 20% h2o2 could redissolve precipitated gold later when rinsing with water
*@**6:32**: By boiling your Agua-Regia solution down (Too Much ????) you have changed the PH Levels, thus causing some of the dissolved Gold to precipitate out of solution because the density of your brew is now so low that the Gold has nowhere to go.*
Hot solutions can hold more than cold solutions, like when we were kids we made those rock candy sticks with sugar water that we supersaturated with sugar and when it cooled off the sugar would condense on the stick.
It's absolutely incredible, I'm not sure anybody's documented f****** around with huge amounts of gold before and just seeing what happens, this is amazing research honestly.
Tune in tomorrow for the exciting conclusion. Will our lab coat hero pour a perfect bar? Will he perform another purification and S0² precipitation?
Same Sreet Time
Same Sreet channel
I believe you fully saturated the solution when you boiled it down and crashed gold out of solution by over boiling to a syrup. I recommend figuring out the amount of liquid you will need to keep the gold from crashing out for future experiments. 👍
I always love your vids though, no matter what. Especially when Mrs Sreetips gets involved. 😁
Oh... And you should have added a healthy muriatic dose and then restarted the nitric trickle... Reform aqua regia to re-dissolve the gold. ... For future reference. 🤘
I showed her this comment, brought a big smile, she said thanks!
I dont know why but 18:38 makes me think, "Prospector Sreetips" lol
You mention possible contamination. Was the ice distilled water or tap?
Maybe one of your other ingredient?
How “pure” is your acids or you stump out? Is it possible they had trace contaminates?
Tap water. I think there was some platinum group metals in that gold bar. That would explain the weird layering during the re-hydration and the layering during the precipitation.
That watch is a fine example of the importance of working under a laminar flow hood. Even working outdoors can be dangerous. Yet working indoors without proper ventilation is a slow death wish.
That is terrifying when the unexpected happens during a refining. I just had a disaster happen with a 3 ounce refining where some of the karate stamps where not accurate so I over inquarted. It crumbled and some of it even settled as the purple colloidal gold. My refining turned into a recovery process. Still working on it!
I’ve had that happen
... p.s.: forgot this...
I recommend to stir the solution while precipitate the gokd with SMB. It would take to long to explain, but believe me you will need much less SMB. And its good to save in times like these
Amazing !! Supersaturation of GOLD !!! The gold try to escape
it would be super convenient if in these multi part series, you had the other parts linked in the description
I’ll get to it. After producing four videos in four days, I’m just plain wiped out! I have a severe case of OMS (Old Man Syndrome).
Wicked separation with the syrup and hcl! Almost got messy!
This has got to be the best gold processing video yet.
Sreetips, you actually invented a way to precipitate Gold with Hydrochloric Acid...Brilliant!!!
Forbidden fruit punch. Such a pretty color. Fascinating
I'm not sure.. just thinking a bit. When you dissolve larger batches of Gold it's obvious your concentration of salts increases judging by the colour of your solutions. I think when you percipitate then probably more PGM's percipitate with the Gold.
You’re the first to call it correctly: the gold had PGMs in it.
Yeah I also had the impression this solution was also more red than the orange we are used to of ChloroAuricacid @@sreetips The solution?: Just dilute before percipitation with 4 liters of Distilled water and split the batch up to be safe for boil overs? I see Asian refiners always dilute their solution before percipitation of Gold.
Another amazing video thank you for showing us these things also on top of that is that 52 oz bar of gold going to be a giveaway LOL I know better than that just a joke sir I hope everything continues to be well for you and your family and happy New Year's to you
1:23 it would be nice to know the water displacement of the gold bar prior to you putting all that in solution.
looks like you boiled it down to beyond saturation and when you added the acid it caused the molecules to come out of solution.
Very neat reaction. Didn't see that coming
Probably a stupid question. When you said there might be contaminates. The ice cubes you were using. Were they from distilled water? Would that mean the difference? I don't know. Just wondering. Enjoy your video's. Thanks again. 😎👍🇨🇦
He uses distilled water
No, contaminants in tap water are parts per million. I think the gold bar had some PGMs (Platinum Group Metals).
I’ve since switched to tsp water. Not enough junk to affect a precious metals assay.
Hope you go a bit hotter on the gold melt next bar, so you can avoid some of the banding from the last bar.
At my level (amateur) that’s the best I’m going to get
I dig the John Wayne gloves. Nice work Mr. Sreetips.
Very cool episode today sreetips
Thanks