I've worked as a professional chemist and as a teacher, but I've always loved chemistry as a hobby.
Figured it would be nice to share with those interested :)
I've got no agenda, no real plan, I just do whatever seems fun to me on any given day. With that in mind topics will bounce around a lot and I might shelf a project for months before coming back to it... Might even sometimes stray away from chemistry.
Subscribe if you like what I do, or consider becoming a member on here or a patron if you're feeling extra generous.
Feel free to ask me anything (legal) in the comments and I'll do my best to respond!
NOTE: Nothing on this channel should be attempted or recreated without professional training or unless I specifically state otherwise in the specific video. Many of these procedures are EXTREMELY dangerous without professional training/supervision.
PS: Do not contact with any requests regarding controlled substances. I will not respond.
Пікірлер
Effects like ghb?
I would like to know more about platinum cure silicone . as well as how to stop cure inhiation like how/what's in inhibitx . thank you for a great video
I don't think your explanation and the reaction given are true. First, any crosslinking would require a molecule with at least two functional groups, and ethanol has only one. Second, your reaction has oxygen as a product. Ask yourself - is really any gas produced? Keep in mind that the stoichiometry you've provided dictates that for each mole of ethanol reacting (ca. 50 ml) you'd get over 20 liters of oxygen. That's quite an off-gas, I'd say.
Cat litter to silicone would make a catchy title.
I’m just here for the software optimisation content 🥲
It would have been nice to see some qualitative analysis of the end and product and intermediates to proove it's a fully substituted product.
I inhaled that yellow gas much, years ago
What about a coffee maker and.. never mind 🤣😭😭😂😂😭😭😭
I read it as Making SIlicon and I was like huh? we are going to journey to a star today
i remember when i mixed NaOH sol with SiO2 kitty litter, i would usually find a thick disc of some kind of SiO2 polymer at the bottom, it was quite heat resistant. some crude aerogel
the Best Synthesis Clip ever,.....
What happens if you replace the ethanol with a different alcohol, like methanol or isopropanol?
Definitely a useful material. I wonder how much the process could be adapted, such as producing a slower curing pourable mix, or maybe making a gel or a foam?
I wonder how well alcohol would permeate without agitation. Could put the sodium silicate in a mold and add the alcohol on the surface. Or more likely, use this to make thin sheets.
What reaction is used in RTV silicones?
Do it's physical properties make it a non Newtonian solid? Lol
Very interesting! What would happen if you use a longer alcohol for linking? Something like polyethylene glycol?
Cool! 😁😃 So how does high heart resident silicone work!?
As a kid, I loved throwing bouncy balls to confuse my cat at playtime.
Are you sure you are producing oxygen as a side product? To me it looks a bit sus that you are making Si-C bonds that easily. It looks more like Si-O-C, which would not produce oxygen gas, and is thermodynamically more favorable too.
How does this relate to silicone lubricants.
Video with the acetate method. DIY Silicon Caulk!
Sodium metasilicate (crystalline Na2SiO3) isn't usually sold to regular customers as it is because it's corrosive. If you bought your waterglass at a hardware store, it probably is an amorphous silicate variant much more rich in silica which is safer to handle. It is also good for making bouncy balls, though. When I was in middle school I used to make them all the time from silica-rich waterglass and denaturated alcohol. Now I wonder what happens if I use metasilicate.
Like this comment
I did this in an oven, heating the calcium sulfite and sodium nitrate to 250C for an hour, packed down in the glass container and covered with 2 layers of foil to slow down the oxidation of my product. Once complete, I did the sulfuric acid test on the unprocesses product and it spontaneously produced the NO2 gas. However once I removed the sulfate/sulfite and recrystallized the product from water it doesnt pass the sulfuric acid test unless heated, implying its nitrate. My final product is a very slightly yellow crystalline powder, which could be nitrite but without evolving the NO2 from reaction with H2SO4 at room temperature I'm thinking its nitrate. Any suggestions as to why I passed the H2SO4 test before purifying the product, but not after?
I may be stupid but how does sodium hydroxide dissolve silicon dioxide which is just glass?
Strong alkalis just dissolve silicon dioxide creating silicates. Molten NaOH easily dissolves glass and concentrated NaOH solutions can dissolve regular sand under high pressure. If silica is in the form of silica gel it is even easier, you can easily dissolve silica gel cat litter in concentrated sodium hydroxide solution. It's an acid-base reaction, silicon dioxide is a very weak acidic oxide.
NurdRage covered the reaction in his sodium series. It's a common problem when working with NaOH, especially at higher temperatures. -- it likes to dissolve your glassware unless you completely eliminate water from your reaction. I've lost a few flasks to it. NurdRage starts his reactions by destroying ALL of the water with sodium metal.
I just went down a bit of a rabbit hole on the subject of silicone's environmental impact. It's a mixed bag, but not an unmanageable one the way plastic is. It generally breaks down even slower than plastics (I'm sure there are exceptions due to how varied both can be), but that can be a positive for reusable items. It's terrible for disposable items, but ffs we gotta stop with that anyway. But at EOL, it can generally be incinerated safely, unlike plastic, since it mostly produces sand, carbon oxides and water, unlike all of the plasticizers and softeners and adjuncts added to make most plastics useful. Sure, produces carbon dioxide and monoxide, but compared to plastics... Not that it create much energy when incinerated, but the toxic outgassing is less. In a future without plastics, maybe we'd use more silicone and have a collection system for it so it goes into incinerators instead of landfills? Or maybe we'd find a recycling system that uses it as a relatively clean source of silica for glassmaking or more silicone?
I tried this with potassium silicate, but it didn't work.
Where did you hear that you can put alkanes into silicates like that? I am pretty sure what's going on is alkoxide formation with the ethanol, which then condense with silanols.
I think you're right.. honestly I just took the word of a paper I found and when I couldn't make the mechanism work myself I just figured the author knew better than I did. Should have added some disclaimer about my uncertainty.. I'll look into it a bit more but your idea sounds much more feasible as a mechanism. Weirdly there's not a ton of info on this process despite it being so simple and accessible
@@integral_chemistry Ah yeah, I was wondering if there was something I missed, would be neat to turn Q groups into T or D groups like that...
honestly....didn't know that a "modified Silane" is still more or less silicone... I'm a boatbuilder and a lot of "marine-grade (/-fit) polymers are silanes....like "bostik" or "Sika-Flex" kinda shook thats its still basically silicone....sure there are differences but its always like "no don't use silicone, use this-and-that" chemically at least similar....very interesting care to make a video on the "marine sealants/ caulks"? I for one would find that highly entertaining :)
Yes, so many plastics are just slight variations on side chains used. Sometimes they can have quite dramatic effects!
Lookup the incredibly weird "Silicones, the answer"
Well.... that was certainly a thing. Well worth the brain damage, i'm sure...
Hey man, just wanted to say you kind of cracked open the world of chemistry for me and i love you for that, thank you.
Could the reaction be something like this? 2 Na2SiO3 + CH3-CH2-OH → NaSiO2-CH2-CH2-NaSiO2 + 2 NaOH + 1/2 O2
Or this? 12 Na2SiO3 + 7 CH3-CH2-OH → 6 NaSiO2-CH2-CH2-NaSiO2 + 8 NaOH + 2 Na2CO3 + 5 H2O
great. now my fuck dolls are bouncy..
Please explain to me how ethanol can crosslink your polymer? it looks like you are making and partially hydrolysing tetraethoxysiloxane?
Also you do not have any Si-C bonds as far as I can see, does this qualify as a polysiloxane?
That's actually a good question.. let me go back to the little paper I found on this and see if I can come back with a good answer. Technically this was from what looked like a undergrad-level lab activity, and I wasn't actually able to find any formal literature on this reaction. I'll look into it a bit more and see what I can find
@@integral_chemistry you can use cyclopentadimethyldisiloxane (dimethicone) and some catalyst to do it pretty easily :) nit/lice removal solution is mainly that
sihg!
How can Si-O bonds turn into Si-C bonds from Na-silicate and EtOH? I think there is something wrong with the mechanism, and no cross linking could be explained like that either. Could you provide any reference? Thank you for all the chemistry on this channel!!!
No problem at all! And yeah I spent about an hour last night toying with this reaction to try and make it make sense to me, as I always assumed cross-linking could only be achieved by acid hydrolysis. In the end I just decided to copy the mechanism from my source instead of trying to make my own.. Anyway yeah I'll try and put the link in the video description, maybe someone else can sus it out.
so you're telling me sand+drain cleaner+booze makes a bouncy ball?
Yessir! I almost did this video starting from sand but I decided to keep it short
So that's why silicone caulk smells like vinegar.
Yes exactly!^ I didn't even know why until I did this video
How is ethylamine made tho
Near where I live there was an armaments works during WW1. A fire started in some empty sacks which ignited sacks full of TNT, which started an exponential burn which resulted in a detonation of a few hundred tonnes of TNT killing 108 people. So if you have enough TNT stacked together and set light to it then it can detonate. I'd guess that with a large enough mass the flame front accelerates into the mass until it goes supersonic.
This reminded me of the movie FLubber.
Dude I totally forgot about that movie 😅
Cool, now try making silicon from scratch
Oh christ 😅 honestly a thermite-type reaction could do it, the tough part would be collecting it afterward
@@integral_chemistry The longer the cooling time the larger the silicon pieces. You can also recrystallize silicon from molten metals like molten zinc, that way you can extract it from the reaction mixture.
This is such a PERFECT video for people to actually replicate as their first home chem project
Right? I've been wanting to do more accessible stuff lately as I realized I've been straying into projects no normal person would ever be able to put together at home, and the initial point of the channel was to try and make chemistry more accessible 😅
Daaaamn i'll give this a shot when back home
Lmk how it goes!
Wait... it's that simple? Now I wonder if any medieval alchemists managed to make silicone that way. The ingredients have been readily available for centuries.
I hadn't thought of that but maybe. I'm curious now how long ago they discovered that you could dissolve silicon dioxide in lye.. that would definitely be the tougher part I'd think
I doubt it. We have the distinct advantage of good pure reagents these days. That's relatively recent. They certainly didn't have pure ingredients in the middle ages.
@@nolanwhite1971Lye, silica, and ethanol have been available in high purity for quite some time tho
@@integral_chemistry Earliest reports of dissolved silica goes back to the 1500s, though waterglass was only properly studied in the 1800s.
@@nolanwhite1971 alchemists' had quite pure H2SO4 for a long time, but I am not sure about NaOH. Most old NaOH/KOH making processes are heavily contaminated with NaCO3/KCO3, good for soap making, but would produce contaminated water glass, which can be cleaned but I don't think they knew or cared much. They had really pure 96% alcohol though, but they did not have any 100% ethanol.
Neat, I didn't really understand silicone polymerization mechanism (not that I tried, but still). I see, that during actual polymerization the silicone loses water, but I am wondering, what prevents single silane molecule to lose water and become like ketone (dimethyl silanone). And if it does only tiny bit, why is this not preferred.
I'll be honest I'm still struggling to understand this mechanism myself. I tried for a while last night to put my own version together but I couldn't balance it, nor explain electron movement. In the end I just gave up and copied the mechanism from the literature. I'll probably just post a link in the video description and see if anyone else can figure that one out
This looks really cool and all, however, I didn't understand a single concept, yet the bouncy ball kept my attention the entire time. 😅
LMAO it was surprisingly fun to play around with. Took me until this video to realized I haven't played with one of these in years
@@integral_chemistry 1 inch bouncy balls were in gum ball type of vending machine for 25 cents as a kid. Kinda learned geometry and not to bounce it around the house. The one thing I remember is when the ball bounced it would reverse the spin. Like it could grip the surface and put the energy into reverse spin. They were fun to play with my friends and the game was don't look stupid trying to chase the ball. We had a lot of fun chasing around the ball and laughing at each other. Thank you 🙏
What would happen if you used sugar alcohols instead of ethanol?
I don't think it would work tbh. I tried a few other alcohols and each time I just got a sort of noncohesive slime.. which I guess was cool in it's own way tbh