Really great videos, very comprehensive and well explained. I'm surprised there aren't more subscribers to the channel. I will say however that I'm glad you shortened the intro, the old one was a bit too loud and long and I always had to skip it.
I have used a nitrile glove with a small hole slit into it as a gasket for vacuum filtration when my büchner ring broke. It worked quite well in a pinch.
It can sometimes be used ok, but as you can see from this video it usually results in a rather crappy vacuum filtration. The air gets in around the sides and ruins the vacuum. That's why you're taught to use the correct filter size for vacuum filtrations. But sometimes it does make things easier (when you're priority isn't to get the best vacuum filtration).
great vid interesting I tried this myself using nickel 2 chloride and alu foil reacting it with hci and water to form the ni metal, althought didn't know your suppose to charge it with a base before use no wonder it didn't work look forward to the follow up vid.
Interesting. I wonder if this procedure would produce pyrophoric and very finely divided Mn, V, Co, Cr, Ti, and lanthanide metals (e.g. Ce) from their oxalates?
The reduction potential for Oxylate is -.44 volts which is the same for Iron. Driving off CO2 helps force the reaction to metal. Zinc and Chromium are -.76 volts so probably mostly oxide result. Interesting if this method yields alloys for metal mixtures like heating Tin Oxalate (-.1) with Copper Oxalate (+.3) to make bronze.
An excellent vacuum vessel is a pressure cooker. I have used a pressure cooker and a vacuum pump for refrigeration to save two cell phones that have been dropped in water With excellent results.
You should really start doing the glassware/chemical unboxings you've been mentioning. You could also do a NurdRage inspired video and going through the essential lab equipment. :)
Did you get around to using the decompensated nickel oxalate as a catalyst? If so, how did that work out? Was thinking about doing something very similar...
Oh, but why wasn't nickel(II) chloride available for you? I remember my local chemical vendor selling a very old bottle of nickel(II) chloride at quite a loss. Usually it's about $18 dollars converted from my currency, but she sold it at, I remember, $9-$10 for 500g
Hi Doug! Can we talk directly? I have some insider knowledge of this stuff and I’m very interested to know uses, toxicity’s, and the complexity of recreating what you’ve done here! Hope to hear soon!
Love your vids vary well done! As for speeding up drying you might try using a stoneware Crockpot with a layer of sand or salt between your drying plate instead :)
Doug's Lab Cody from Cody's Lab uses that method especially to evaporate the nitric from gold solutions. Just be carefull-the metal edge tends to rust when exposed to acid.
Dont get stoneware. It can and will easily break. Get a corningware pyroceramic dish. It can survive hell and back. And can even be directly used for evaporation and/or drying. It is used by me, religiously. Search goldrefiningforum.com for 'corning pyroceram' and a "whats what" thread will be shown with tons of info on them
I always wanted to try to make Raney Nickel the traditional way but never got around to it. It can't be that hard to make a 50-50 alloy of aluminium and nickel yet I've never seen anyone try it, neither on youtube or on message boards. I was thinking either to heat a half half mixture of finely divided aluminium and nickel in a crucible with lid flushed with welding-grade argon in a homemade PID-controlled (20$ ebay china) ceramics oven (using Kanthal resistor wire), or to heat said mixture using an induction coil. Once you have the NiAl alloy it merely requires crushing it up and digesting in 20% NaOH to dissolve the aluminium in the alloy and you're left with classic Raney Nickel, also very pyrophoric.
Can it actually be used as a substitute for nickel in the hydrogenation of gasoline? How can the catalyst be recovered after hydrogenation back to nickel?
@@DIGITALVHS Probably to make some MDMA lmao. I guess the pyrophoric nickel could be used on the methylenedioxy-phenyl-2-nitropropene in place of the usual Pd/C, Raney nickel or mercury amalgams for the last step of the synthesis; reduction to the amine.
I have analar grade Nickle chloride, over a Kg of the emerald green, and yes, your solution was a very "dirty dark green"..so I imagine you are right, it was not all that pure, also, if you had pressed that paper catch towel down snug into the circumference of the Buchner filter..( and that's pronounced "Bookner" not "buke ner" by the way) it would have helped your filtration by stopping air leaks..are you using a water aspirator for your vacuum?..it's never much good with fine ppt's like that..
Hi Doug, I probably missed the explanation, but when you made the fine nickel powder, does it need to be hot to self ignite in air as you demonstrated, or would it ignite at room temperature? If you let it cool, would it oxidize relatively quickly, or could you store it for a long time?
+Dana Wold With pyrophoric iron made from oxalate you can make it and then seal the test tube with a waxed cork and sprinkle the iron the next day from a cold test tube and it will still produce a shower of sparks. You just melt some wax from a burning candle over the cork and then press the cork into the test tube making an airtight seal. With nickel it isn't safe to breathe any of the nickel oxide smoke. See page 3. nj.gov/health/eoh/rtkweb/documents/fs/1341.pdf
+Dana Wold I don't know about nickel but pyrophoric iron made from the oxalate, by melting some wax from a burning candle over a cork and then pressing the cork into the test tube it will keep for the next day. Sprinkled from a cold test tube, it will still make a shower of sparks. You wouldn't want to breathe the smoke from burning nickel though. See page 3 - Fire Hazards nj.gov/health/eoh/rtkweb/documents/fs/1341.pdf
Heating Nickel Oxalate gives just Nickel and CO2. The citric won't decompose cleanly and gives maleic acid nickel salts. Nickel Formate broke down into Nickel Hydroxide and Carbon Monoxide et al. We used ctric acid in our gold plating tank as sacrificial chem at anode.
Please can you help me with my project? I want to produce a chemical name is potassium tetraoxalate dihydrate and I dont know manufacturing process or any possible catalyst mabe used in this process. I have spent a year and found nothing about this process. Please help me I'm really frustrated
Adding Sodium Borohydride solution precips Nickel Boride Hydride which is more active than Raney Nickel. Also borohydride is an easy source of Hydrogen.
+Doug´s Lab What do think about posting a video on how to make a beautiful lime-green light-sensitive complex compound called potassium ferrioxalate trihydrate? If don´t know what it´s needed besides oxalic acid, I can tell you.
@@petevenuti7355 Yup, small crystals and solutions of ferrioxalate are light sensitive, decomposing into ferrooxalate, oxalate and carbon dioxide. If you leave it exposed to UV a lot longer you will eventually be left with iron(III) hydroxide.
Raney alloys are just that, not pure Nickel. The product of digesting NiAl with NaOH is Ni5Al but Al can be replaced with La or Ca. Ni5Ca was the metal hydride storage for nickel metalhydride batteries (other electrode in battery is NiO2. Raney alloys can also be non-nickel like FeTi (which has the highest Hydrogen storage).
Llizard CZ White phosphorous is in a higher orbital state and is therefore less stable than red phosphorous.It seems like it would automatically decay but i guess not.
Random Experiments International You don't need pressure or days...I have done it before by heating red phosphorous in an inert atmosphere with a torch for only a few seconds.
Really great videos, very comprehensive and well explained. I'm surprised there aren't more subscribers to the channel. I will say however that I'm glad you shortened the intro, the old one was a bit too loud and long and I always had to skip it.
+Xei I agree! Glad you like the change. I'm always listening :)
I have used a nitrile glove with a small hole slit into it as a gasket for vacuum filtration when my büchner ring broke. It worked quite well in a pinch.
love the coffe filter in the buchner idea. going to steal that and use it for silver cement. much obliged!
It can sometimes be used ok, but as you can see from this video it usually results in a rather crappy vacuum filtration. The air gets in around the sides and ruins the vacuum. That's why you're taught to use the correct filter size for vacuum filtrations. But sometimes it does make things easier (when you're priority isn't to get the best vacuum filtration).
great vid interesting I tried this myself using nickel 2 chloride and alu foil reacting it with hci and water to form the ni metal, althought didn't know your suppose to charge it with a base before use no wonder it didn't work look forward to the follow up vid.
Great video ! I wonder what kind of reaction (reduction ?) you'll be doing with this Nickel catalyst and H2 :D
Question: isn't the metal hydride in Nickel Metal Hydride batteries the same as Raney Nickel hydrogenation catalyst?
Interesting. I wonder if this procedure would produce pyrophoric and very finely divided Mn, V, Co, Cr, Ti, and lanthanide metals (e.g. Ce) from their oxalates?
The reduction potential for Oxylate is -.44 volts which is the same for Iron. Driving off CO2 helps force the reaction to metal. Zinc and Chromium are -.76 volts so probably mostly oxide result. Interesting if this method yields alloys for metal mixtures like heating Tin Oxalate (-.1) with Copper Oxalate (+.3) to make bronze.
An excellent vacuum vessel is a pressure cooker. I have used a pressure cooker and a vacuum pump for refrigeration to save two cell phones that have been dropped in water With excellent results.
Good and very much useful video for me
Nickel oxalate used as a catalyst in vegetables oils hydrogenation process???
You should really start doing the glassware/chemical unboxings you've been mentioning. You could also do a NurdRage inspired video and going through the essential lab equipment. :)
+WeekendScience Sounds like a good 2500 subscriber special!
Did you get around to using the decompensated nickel oxalate as a catalyst? If so, how did that work out? Was thinking about doing something very similar...
Nice experiment! I'd be afraid of those highly toxic particles of nickel oxide.
Nickel is more toxic to women than men.
Did you ever do anything with the Nickel Oxalate? It would be nice to see a hydrogenation using fine Nickel particles.
I want to information about nickel oxalate? Can you help me
Oh, but why wasn't nickel(II) chloride available for you? I remember my local chemical vendor selling a very old bottle of nickel(II) chloride at quite a loss. Usually it's about $18 dollars converted from my currency, but she sold it at, I remember, $9-$10 for 500g
Hi Doug! Can we talk directly? I have some insider knowledge of this stuff and I’m very interested to know uses, toxicity’s, and the complexity of recreating what you’ve done here! Hope to hear soon!
99% nickel welding rods would be a good thing to use.
Really
Love your vids vary well done!
As for speeding up drying you might try using a stoneware Crockpot with a layer of sand or salt between your drying plate instead :)
+Adam Outlaw Hmm, I'll have to keep an eye out for one of those at the thrift store.
Doug's Lab Cody from Cody's Lab uses that method especially to evaporate the nitric from gold solutions. Just be carefull-the metal edge tends to rust when exposed to acid.
Dont get stoneware. It can and will easily break. Get a corningware pyroceramic dish. It can survive hell and back. And can even be directly used for evaporation and/or drying. It is used by me, religiously. Search goldrefiningforum.com for 'corning pyroceram' and a "whats what" thread will be shown with tons of info on them
I always wanted to try to make Raney Nickel the traditional way but never got around to it. It can't be that hard to make a 50-50 alloy of aluminium and nickel yet I've never seen anyone try it, neither on youtube or on message boards. I was thinking either to heat a half half mixture of finely divided aluminium and nickel in a crucible with lid flushed with welding-grade argon in a homemade PID-controlled (20$ ebay china) ceramics oven (using Kanthal resistor wire), or to heat said mixture using an induction coil. Once you have the NiAl alloy it merely requires crushing it up and digesting in 20% NaOH to dissolve the aluminium in the alloy and you're left with classic Raney Nickel, also very pyrophoric.
Induction coil sounds better. Please post it if you do it!
Pyrophoric is Raney Nickel which burns with Hydrogen and Aluminum also. Ditto Ni2BH2 (Ni+2 + BH4-).
Can it actually be used as a substitute for nickel in the hydrogenation of gasoline? How can the catalyst be recovered after hydrogenation back to nickel?
Alexander Shulgin
1 year ago
hi doug when you make a hydrogenation?
I second this idea.
With a name like Alexander Shulgin I wonder for what purpose he wants to know that for...
@@DIGITALVHS Probably to make some MDMA lmao. I guess the pyrophoric nickel could be used on the methylenedioxy-phenyl-2-nitropropene in place of the usual Pd/C, Raney nickel or mercury amalgams for the last step of the synthesis; reduction to the amine.
I have analar grade Nickle chloride, over a Kg of the emerald green, and yes, your solution was a very "dirty dark green"..so I imagine you are right, it was not all that pure, also, if you had pressed that paper catch towel down snug into the circumference of the Buchner filter..( and that's pronounced "Bookner" not "buke ner" by the way) it would have helped your filtration by stopping air leaks..are you using a water aspirator for your vacuum?..it's never much good with fine ppt's like that..
Thanks for making these videos, their awesome!
+grouchfan Thanks for watching my videos. You're awesome! :)
Hi Doug, I probably missed the explanation, but when you made the fine nickel powder, does it need to be hot to self ignite in air as you demonstrated, or would it ignite at room temperature? If you let it cool, would it oxidize relatively quickly, or could you store it for a long time?
+Dana Wold With pyrophoric iron made from oxalate you can make it and then seal the test tube with a waxed cork and sprinkle the iron the next day from a cold test tube and it will still produce a shower of sparks. You just melt some wax from a burning candle over the cork and then press the cork into the test tube making an airtight seal. With nickel it isn't safe to breathe any of the nickel oxide smoke. See page 3. nj.gov/health/eoh/rtkweb/documents/fs/1341.pdf
+Dana Wold
I don't know about nickel but pyrophoric iron made from the oxalate, by melting some wax from a burning candle over a cork and then pressing the cork into the test tube it will keep for the next day. Sprinkled from a cold test tube, it will still make a shower of sparks. You wouldn't want to breathe the smoke from burning nickel though. See page 3 - Fire Hazards
nj.gov/health/eoh/rtkweb/documents/fs/1341.pdf
can we prepare his fine powder for other metals like this?
Instead of oxalic acid. I will use citric acid to make nickel citrate???
It s possible pllz tell me sir
Heating Nickel Oxalate gives just Nickel and CO2. The citric won't decompose cleanly and gives maleic acid nickel salts. Nickel Formate broke down into Nickel Hydroxide and Carbon Monoxide et al. We used ctric acid in our gold plating tank as sacrificial chem at anode.
Pls one day u put hydrogenation of vegetable oil(triglycerides )oils process video.thank u sir
Please can you help me with my project? I want to produce a chemical name is potassium tetraoxalate dihydrate and I dont know manufacturing process or any possible catalyst mabe used in this process. I have spent a year and found nothing about this process. Please help me I'm really frustrated
Good afternoon. Tell me what color should be the nickel powder is pyrophoric?
hi doug when you make a hydrogenation?
Free my nigga Chem Player!
@ What's the problem with showing, for example, the hydrogenation of 2,5-dimethoxynitrostyrene?
Sir,make Vidio for hydratropik aldehyde.
Adding Sodium Borohydride solution precips Nickel Boride Hydride which is more active than Raney Nickel. Also borohydride is an easy source of Hydrogen.
I stand out in the hood. Last time I loaded up my glass, burner and stirrer a drive-by happened.
Have you tested the catalytic activity? How?
I too bought one of those Crappy-ASS Filter aids. Much better to use a rubber stopper with a hole in it.
+Doug´s Lab What do think about posting a video on how to make a beautiful lime-green light-sensitive complex compound called potassium ferrioxalate trihydrate? If don´t know what it´s needed besides oxalic acid, I can tell you.
Light sensitive?
@@petevenuti7355 Yup, small crystals and solutions of ferrioxalate are light sensitive, decomposing into ferrooxalate, oxalate and carbon dioxide. If you leave it exposed to UV a lot longer you will eventually be left with iron(III) hydroxide.
hope you don't mind me asking but what was your percent yield?
Does that work for zinc oxalate as well?
Is Doug Cody's little brother?
is this known as raney nickel
Raney alloys are just that, not pure Nickel. The product of digesting NiAl with NaOH is Ni5Al but Al can be replaced with La or Ca. Ni5Ca was the metal hydride storage for nickel metalhydride batteries (other electrode in battery is NiO2.
Raney alloys can also be non-nickel like FeTi (which has the highest Hydrogen storage).
Is that lime green color Nickel Carbonate's usual color?
+Erik Probably since it's Pottery grade, it's surely used in pottery glaze to give a green color !
Do you know of any ways of reducing white phosphorus to red phosphorus?
You cannot reduce white phosphorus into red as far as i know they are both in the same oxidation state.
Llizard CZ White phosphorous is in a higher orbital state and is therefore less stable than red phosphorous.It seems like it would automatically decay but i guess not.
+Magneto! White phosphorus is turned into red phosphorus by heating it under pressure for days. That's quite difficult to achieve in the home lab.
Random Experiments International You don't need pressure or days...I have done it before by heating red phosphorous in an inert atmosphere with a torch for only a few seconds.
+Magneto! You're talking about turning red to white phosphorus. That's very easy, but you want to do it the other way around.
Buy yourself a set of nesting rubber funnel adapters off eBay, Doug. That flat thing you used for the filtration is atrocious.
Ditch the rubber ring and get a rubber stopper with a big hole in it?
Why couldn’t you just add a solution of oxalic acid to the nickel carbonate?
It would form a mix of side products that would be a pain to separate.
Colgate toothpaste
Wth who unsubscribed me from the channel?
Stop please, for all of our sanity
balance your equations REEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEE