With a tweak to the setup.and electrodes used, one can make many of their own common cleaners as DIY projects, such as NaOH, HCl, and ammonia cleaner/disinfectant like lysol, mopping cleaners, mold/mildew remover, Clorox etc etc. Though it wont b exact, the main active chemical can be made for basically all items like this and with it being stronger it's just as, if not more so, effective. You can even use made NaOH to make your own soap easily, which works MUCH better than store bought which is mostly fillers and very little actual soap. Can be used for dishes, hand soap, or even laundry and what I've made is more potent than the "Gojo" hand cleaner/grease remover that's super expensive anyone ever covered in grease from car mechanicing will know what that is. But mine cost about 16 cents to make, just a few days of patience. I have a channel but all my content was basically removed because of stupid reasons...I dont make content though I'd like to. If ppl were interested in something like this, I could attempt a little mini series on how to
@ckimsey77Ай бұрын
n1msu: drain cleaner is usually 5% NaOH, so this would probably get u to that maybe a little higher, but u cant make concentrated NaOH this way as the product equilibrium is based on the salt concentration when a proper salt bridge isnt used (see my full explanation comment below). However, being highly contaminated with salt and at low concentration (drain cleaner also contains proteins/digestive enzymes and catalysts that aid in making it much more effective) it wouldnt work very well as this use. Concentrated hydroxide, however, will power through nearly anything on it's own, but this particular method would not get you there. Buying pure NaOH sid pellets is quits cheap by the pound, so u can dissolve and make your own pure NaOH solution as weak or strong as u want...juzt add and dissolve slowly if making very concentrated....NaOH dissolving releases tremendous beat, and too much too fast can heat the water to the point of boiling or melting its container ic plastic (dont use metal with con. NaOH ESPECIALLY aluminum, use plastic or glass, preferably glass if being stored) High con. NaOH of pH 12.5-14 will even eat away and etch pyrex chemistry glassware which is VERY chemically inert obviously, if heated and left in long contact. Hot chemicals are super dangerous, WAY more so than same at room temperature as heat increases reaction rate by magnitudes...roughly doubling the rate every 8-10 degree increase. This is why a very cold battery wont hardly put out any current bc the rate is decreased thousands of times over due to temp. decrease. So if you ever attempt to boil down NaOH solution to concentrate it, be VERY CAREFUL and use protective gear as this splashing on you will not end well (if NaOH gets in your eye, it most likely will do permanent damage and can cause complete blindness if not cleaned out immediately). Besides the super acids, strong bases like NaOH is actually way more harmful to you than acids as they react with more tissue types at a much higher rate ESPECIALLY EYES. Acid in eyes is bad, but if rinsed out quickly you'll b fine...NaOH in eyes your screwed Whatever you do, please NEVER try to concentrate sulfuric acid by boiling... first off it wont work unless done in proper distillation set up with the full works of lab glassware contained/set up properly with all needed equipment, and mainly if tried not contained....the boiling point is well above 300 degrees C, and H2SO4 has a bad tendency to superheat, getting hotter than its boiling temp then suddenly violently boiling/splashing out all at once. Boiling sulfuric not only would cause bad burns as a liquid contact at nearly 500 degrees, but the reaction rate at that temp would near instantly start dissolving tissues rapidly. It would be a bad time for sure...
@ckimsey77Ай бұрын
Reply to Anarhuseynow's comment and ppl's. ?s below it. Hes *mostly right, a "salt bridge" is needed to generate NaOH in one and HCl in other...the coloration of the side bubbling chlorine is due to dissolved Cl2 in the solution. Bleach, or sodium hypochlorite, is an ionic species like NaCl and is colorless in water...the Cl2 is the color source. Now why "partial" correct....at low salt concentrations you oxidize 2 water molecules at + terminal (remove electron) generating O2 gas and 4 H+ ions due to electron loss. Equally 4 electrons must be given to solution because 4 was removed at + terminal, so the - terminal reduces 2 waters into 2 H2 gas molecules which bubble out and 4 OH- hydroxide ions. Notice total charge remains neutral as 4 H+ and 4 OH- were generated...but this isnt what we want because we want NaOH not H2 gas, yet these H+ and OH- will simply react back into 4 H2O molecules. The salt bridge prevents the OH- from migrating toward the + terminal and likewise the H+ from attracting toward the - terminal preventing the H+ and OH- from being able to come into contact. With a real salt bridge, this isolated the cells from mixing while allowing current flow, so H+ stays in its side generating HCl, and other side keeps its OH- generating NaOH...so u make hydrochloric acid and sodium hydroxide win win...(the membrane allows selectively passage of Na+ and Cl-, which will switch sides as the H+ and OH- build up to maintain neutral overall charge in each half cell). His piece of foam/cotton or whatever is NOT an ion exchange membrane or proper salt bridge, in other words it wouldnt stop the H+ from going to the - terminal and reacting with the OH- back into water. The reason he still gets NaOH isnt because his salt bridge works at all, but notice I said above a "weak concentration" of NaCl....with a minuscule amt of dissolved Cl- from the salt, theres billions times billions of water molecules in contact with the + terminals service for every one Cl- ion. So the chances a water is oxidized is nearly 100% since theres so many more in contact (the few Cl- will be oxidized as well, but when it is a highly unstable Cl free radical is generated which quickly chain reacts w surrounding water which eventually leads to a H+ anyway and reforming the Cl-). As in a concentrated salt suction used here, the negative Cl- is attracted to the positive terminal and all of them diffuse toward it. When dissolved salt concentration is high enough, all the Cl- migrate to the + terminal and surround it pushing back the H2O molecules which are overall charge neutral and not attracted to the terminal. Here, there's mich more Cl- in contact with the electrode material than water, so more Cl- gets oxidized...and since the concentration of these is very high, it's much more likely the generated Cl free radical finds another Cl free radical just generated beside it than a water molecule, so the two Cl radicals combine into Cl2 gas and dissolve into the water eventually escaping as Cl2 gas (Cl2 is soluble in water, but not by a large amt so most leaves as Cl2 gas). Since we have Cl- being removed as Cl2 gas, we now are generating a net + charge in the cell as - charges are removed at the + terminal (remember b4 H+ was being generated here) and negative charges (OH-) are being generated at the other. Since Cl- is being removed, the Na+ has lost its negative partner as table salt and now will pair with the new made OH- instead generating our NaOH. To balance charged species though, a hydroxide anion must be generated for every Cl- removed. A few H+ is still made which neutralizes a few of the OH- back into water, so without a salt bridge this process is inefficient because energy is being wasted creating undesired side reactions...and as it runs and Cl- concentration falls, more and more O2 gas and H+ will be generated at the terminal reacting more and more OH- back into water further decreasing efficiency and wasting electricity. Theres no need to even bother using 2 separate containers if u just desire NaOH and can properly vent the Cl2 gas safely, and dont mind a little extra power consumption from the inefficiency...as I've examined his "salt bridge" is doing nothing here...its the high salt concentration that's favoring Cl2 generation over O2 and H+ causing NaOH to be generated. However keep in mind in this method your end result solution, though caustic with the desired NaOH, will be highly contaminated with unreacted NaCl salt and dissolved Cl2 gas. The Cl2 can be driven out with heating, but separating the NaCl out from the NaOH is for the home hobbyists quite impossible. For a much more pure end product a proper salt bridge ion exchange with separate cells must be used, or the chloromercuric cell (not sure of exact name, but uses single cell with mercury and works on different mechanism, but will create high purity and results). Hope that helped answer you guys questions under this posters comment, as I didnt see that he had ever responded with an explanation. I am a R&D chem. engr. so if anyone has questions feel free to ask I'll be glad to help. Have a good one you guys
@AliciaDenizzzАй бұрын
So not iodized salt is the one that isn’t like sand??
@MekdesRedae2 ай бұрын
Can u understand me how it is and what did it make
@nicholsjones2 ай бұрын
Use Liquid Ass for the liquid!! THANKS!!!
@fxeditors3 ай бұрын
Damnnn
@abrahamcarreon-ms8jx4 ай бұрын
We all going to die enyway😂
@NoLimitAyan4 ай бұрын
does this show all colours of PH?
@denelson834 ай бұрын
Same pigment found in red cabbage.
@BHUPENDRAJOGI264 ай бұрын
What's the price of this watch??
@paulissus89745 ай бұрын
How difficult to carry out electrolysis on (NaOH)?
@SexKing-hj9nv4 ай бұрын
From what iv seen people heat the NaOH to boiling point (i think its roughtly 320c) and then apply current to it, sodium metal then forms. Im not sure if thier are any solvents/ electrolytes that can be used to avoid heating the NaOH however you would have no luck with water as the sodium ions would just react with the H2O to reform NaOH, this does however make NaOH a good electrolyte to use if your just trying to make oxygen and hydrogen as it is regenerative and doesn't release toxic gas like table salt!
@ajanthaajai53226 ай бұрын
❤ Amazing..... Awesome guys...
@gunat20406 ай бұрын
Super
@kristelmaefortes84207 ай бұрын
Amazing!
@wscamel2267 ай бұрын
why graphite electrode ?
@user-mh1zp7pv7d6 ай бұрын
Because graphite is a good conductor of electricity cause each carbon has 3 bonds and carbon has four electrons on its outer shell. As only 3 electrons are shared one is free. That's why it's being used.
@_namantharu7 ай бұрын
Me coming here after Watching Dr, Stone😅
@xanninjagaming94547 ай бұрын
Us movement
@macbobXD7 ай бұрын
Pow: you are making a minibomb without realizing it
@doublememes6887 ай бұрын
Output wattage kitni hai?
@Mr.Ak328007 ай бұрын
Does Positive side hydrochloric acid?
@RavindraSingh-jj3scАй бұрын
Nope
@lawabidingcitizen51538 ай бұрын
1kg of caustic soda is like 4€ though, and much less work
@mastermindenterpriseslimit75559 ай бұрын
Guess I'll just go buy some do i can make my damn soap
@mastermindenterpriseslimit75559 ай бұрын
I certainly won't be able to do THIS, correctly...
@arayanchandra48459 ай бұрын
Great guys I loved it! Thank you
@remsangichhakchhuak238410 ай бұрын
Can we use different flowers
@ritika1010010 ай бұрын
But green shows that it's neutral
@ishannilanga250911 ай бұрын
What is the supplied Voltage
@gagnant49 ай бұрын
They used a USB plug so it would be 5V DC @ either .5amps or .9amps
@fernandoalexandrodesouzape796711 ай бұрын
Burning wood is literally making ash and some green house gas
@NeonNanoTech11 ай бұрын
I tried the same experiment and tested presence of sodium hydroxide with aluminum foil nothing happened
@user-es2qs7ne3f10 ай бұрын
And me did it but nothing happened
@babla694209 ай бұрын
You need to boil it at 75° celsius to evaporate water from it to make lye more concentrated. Measure its ph until it reaches 13 or 14
@user-sm4vo9mr7z11 ай бұрын
Can we use this naoh for saponification
@SexKing-hj9nv4 ай бұрын
If you intend to use it for soap I don't see why not if your doing it just becuase you can. the byproducts should all be non toxic apart from hypochlorite that forms from the chlorine, however I think this is a very low amount and is just essentially bleech and while toxic I doubt it will cause harm at this conceneration and would likely react with products in the soap anyway (wouldn't likely really be that toxic unless inhaled or injested even at higher concentrations), the rest of the chlorine should leave the solution as it is gaseous, same with the hydrogen and oxygen that are formed (though not toxic). The only remaining product that could be found would be the starting product NaCl, or table salt, which is obviously not toxic. DO HOWEVER BE VERY VERY CAREFUL WITH WHICH ELECTRODES YOU USE, iron will not last long as it will rapidly rust and leech into the solution, DO NOT BE TEMPTED TO USE STAINLESS STEAL EVER, stainless steel has chromium in it and can easily form hexavalent chromium, an extremely TOXIC and CARCINOGENIC (causes cancer) substance. Some however claim it to be safe for electrolysis of NaOH, but do you really want to take the risk with such a toxic substance? General rule of thumb is dont fuck with chromium unless you really know what you are doing, most labs wouldn't even fuck with some forms of chromium unless they have no other choice! Good electrodes tend to be very expensive like platinum however you can use carbon rods in a pinch but they wont be very good! With sodium hydroxide being very cheap I would suggest you just buy some in bulk (you can get it for under $15-20 a KG with it getting cheaper and cheaper the more you buy) im fairly sure you don't need that much for making soap anyway, I doubt you would save that much money away after factoring in the cost of electricity, even if you exlude the inital costs of the equipment. And you dont risk any exposure to chlorides that could form :)
@janardansingh994611 ай бұрын
We need to give the electricity for how many hours...??
@shreshth6913 ай бұрын
You have to give electricity Until there is salt in the bottle
@BlessedNetha Жыл бұрын
Jesus Christ our Lord and Savior is coming very soon. Please repent and preach the Gospel before it's too late. God bless you all. John 3:16 For God so loved the world, that He gave His only begotten Son, that whosoever believeth in Him should not perish, but have everlasting life. 1 John 5:12 Whoever has the Son has life; whoever does not have the Son of God does not have life. John 8:36 So if the Son sets you free, you will be free indeed. Romans 3:23 For all have sinned and fall short of the glory of God Romans 6:23 NLT “For the wages of sin is death, but the free gift of God is eternal life through Christ Jesus our Lord.” Matthew 11:15 Whoever has ears, let them hear. Revelation 22:12 And, behold, I come quickly; and my reward is with me, to give every man according as his work shall be. Romans 8:28 And we know that in all things God works for the good of those who love Him, who have been called according to His purpose
@RigzangTshomo-co5ul Жыл бұрын
What is the name of paper that you r using
@unknownartistaman786 Жыл бұрын
Thnx
@unknownartistaman786 Жыл бұрын
Awesome experiment and explaination
@petrlaskevic1948 Жыл бұрын
What did you put the usb in? In a computer?
@subhendusarkar9299 Жыл бұрын
Fake
@subhendusarkar9299 Жыл бұрын
Water : salt ratio?
@MANOJKUMAR-ev4gl10 ай бұрын
Depends upon the concentration of water or salt...
@subhendusarkar9299 Жыл бұрын
Chemical reaction formula?
@subhendusarkar9299 Жыл бұрын
GV?
@subhendusarkar9299 Жыл бұрын
Sir calculation
@x86_architecture10 Жыл бұрын
In case you are wondering, in order to convert the sodium hydroxide liquid into a powder, you have to boil the water until all you are left with is lye.
Пікірлер
Thanks :)
Could one use a periwinkle as an indicator?
With a tweak to the setup.and electrodes used, one can make many of their own common cleaners as DIY projects, such as NaOH, HCl, and ammonia cleaner/disinfectant like lysol, mopping cleaners, mold/mildew remover, Clorox etc etc. Though it wont b exact, the main active chemical can be made for basically all items like this and with it being stronger it's just as, if not more so, effective. You can even use made NaOH to make your own soap easily, which works MUCH better than store bought which is mostly fillers and very little actual soap. Can be used for dishes, hand soap, or even laundry and what I've made is more potent than the "Gojo" hand cleaner/grease remover that's super expensive anyone ever covered in grease from car mechanicing will know what that is. But mine cost about 16 cents to make, just a few days of patience. I have a channel but all my content was basically removed because of stupid reasons...I dont make content though I'd like to. If ppl were interested in something like this, I could attempt a little mini series on how to
n1msu: drain cleaner is usually 5% NaOH, so this would probably get u to that maybe a little higher, but u cant make concentrated NaOH this way as the product equilibrium is based on the salt concentration when a proper salt bridge isnt used (see my full explanation comment below). However, being highly contaminated with salt and at low concentration (drain cleaner also contains proteins/digestive enzymes and catalysts that aid in making it much more effective) it wouldnt work very well as this use. Concentrated hydroxide, however, will power through nearly anything on it's own, but this particular method would not get you there. Buying pure NaOH sid pellets is quits cheap by the pound, so u can dissolve and make your own pure NaOH solution as weak or strong as u want...juzt add and dissolve slowly if making very concentrated....NaOH dissolving releases tremendous beat, and too much too fast can heat the water to the point of boiling or melting its container ic plastic (dont use metal with con. NaOH ESPECIALLY aluminum, use plastic or glass, preferably glass if being stored) High con. NaOH of pH 12.5-14 will even eat away and etch pyrex chemistry glassware which is VERY chemically inert obviously, if heated and left in long contact. Hot chemicals are super dangerous, WAY more so than same at room temperature as heat increases reaction rate by magnitudes...roughly doubling the rate every 8-10 degree increase. This is why a very cold battery wont hardly put out any current bc the rate is decreased thousands of times over due to temp. decrease. So if you ever attempt to boil down NaOH solution to concentrate it, be VERY CAREFUL and use protective gear as this splashing on you will not end well (if NaOH gets in your eye, it most likely will do permanent damage and can cause complete blindness if not cleaned out immediately). Besides the super acids, strong bases like NaOH is actually way more harmful to you than acids as they react with more tissue types at a much higher rate ESPECIALLY EYES. Acid in eyes is bad, but if rinsed out quickly you'll b fine...NaOH in eyes your screwed Whatever you do, please NEVER try to concentrate sulfuric acid by boiling... first off it wont work unless done in proper distillation set up with the full works of lab glassware contained/set up properly with all needed equipment, and mainly if tried not contained....the boiling point is well above 300 degrees C, and H2SO4 has a bad tendency to superheat, getting hotter than its boiling temp then suddenly violently boiling/splashing out all at once. Boiling sulfuric not only would cause bad burns as a liquid contact at nearly 500 degrees, but the reaction rate at that temp would near instantly start dissolving tissues rapidly. It would be a bad time for sure...
Reply to Anarhuseynow's comment and ppl's. ?s below it. Hes *mostly right, a "salt bridge" is needed to generate NaOH in one and HCl in other...the coloration of the side bubbling chlorine is due to dissolved Cl2 in the solution. Bleach, or sodium hypochlorite, is an ionic species like NaCl and is colorless in water...the Cl2 is the color source. Now why "partial" correct....at low salt concentrations you oxidize 2 water molecules at + terminal (remove electron) generating O2 gas and 4 H+ ions due to electron loss. Equally 4 electrons must be given to solution because 4 was removed at + terminal, so the - terminal reduces 2 waters into 2 H2 gas molecules which bubble out and 4 OH- hydroxide ions. Notice total charge remains neutral as 4 H+ and 4 OH- were generated...but this isnt what we want because we want NaOH not H2 gas, yet these H+ and OH- will simply react back into 4 H2O molecules. The salt bridge prevents the OH- from migrating toward the + terminal and likewise the H+ from attracting toward the - terminal preventing the H+ and OH- from being able to come into contact. With a real salt bridge, this isolated the cells from mixing while allowing current flow, so H+ stays in its side generating HCl, and other side keeps its OH- generating NaOH...so u make hydrochloric acid and sodium hydroxide win win...(the membrane allows selectively passage of Na+ and Cl-, which will switch sides as the H+ and OH- build up to maintain neutral overall charge in each half cell). His piece of foam/cotton or whatever is NOT an ion exchange membrane or proper salt bridge, in other words it wouldnt stop the H+ from going to the - terminal and reacting with the OH- back into water. The reason he still gets NaOH isnt because his salt bridge works at all, but notice I said above a "weak concentration" of NaCl....with a minuscule amt of dissolved Cl- from the salt, theres billions times billions of water molecules in contact with the + terminals service for every one Cl- ion. So the chances a water is oxidized is nearly 100% since theres so many more in contact (the few Cl- will be oxidized as well, but when it is a highly unstable Cl free radical is generated which quickly chain reacts w surrounding water which eventually leads to a H+ anyway and reforming the Cl-). As in a concentrated salt suction used here, the negative Cl- is attracted to the positive terminal and all of them diffuse toward it. When dissolved salt concentration is high enough, all the Cl- migrate to the + terminal and surround it pushing back the H2O molecules which are overall charge neutral and not attracted to the terminal. Here, there's mich more Cl- in contact with the electrode material than water, so more Cl- gets oxidized...and since the concentration of these is very high, it's much more likely the generated Cl free radical finds another Cl free radical just generated beside it than a water molecule, so the two Cl radicals combine into Cl2 gas and dissolve into the water eventually escaping as Cl2 gas (Cl2 is soluble in water, but not by a large amt so most leaves as Cl2 gas). Since we have Cl- being removed as Cl2 gas, we now are generating a net + charge in the cell as - charges are removed at the + terminal (remember b4 H+ was being generated here) and negative charges (OH-) are being generated at the other. Since Cl- is being removed, the Na+ has lost its negative partner as table salt and now will pair with the new made OH- instead generating our NaOH. To balance charged species though, a hydroxide anion must be generated for every Cl- removed. A few H+ is still made which neutralizes a few of the OH- back into water, so without a salt bridge this process is inefficient because energy is being wasted creating undesired side reactions...and as it runs and Cl- concentration falls, more and more O2 gas and H+ will be generated at the terminal reacting more and more OH- back into water further decreasing efficiency and wasting electricity. Theres no need to even bother using 2 separate containers if u just desire NaOH and can properly vent the Cl2 gas safely, and dont mind a little extra power consumption from the inefficiency...as I've examined his "salt bridge" is doing nothing here...its the high salt concentration that's favoring Cl2 generation over O2 and H+ causing NaOH to be generated. However keep in mind in this method your end result solution, though caustic with the desired NaOH, will be highly contaminated with unreacted NaCl salt and dissolved Cl2 gas. The Cl2 can be driven out with heating, but separating the NaCl out from the NaOH is for the home hobbyists quite impossible. For a much more pure end product a proper salt bridge ion exchange with separate cells must be used, or the chloromercuric cell (not sure of exact name, but uses single cell with mercury and works on different mechanism, but will create high purity and results). Hope that helped answer you guys questions under this posters comment, as I didnt see that he had ever responded with an explanation. I am a R&D chem. engr. so if anyone has questions feel free to ask I'll be glad to help. Have a good one you guys
So not iodized salt is the one that isn’t like sand??
Can u understand me how it is and what did it make
Use Liquid Ass for the liquid!! THANKS!!!
Damnnn
We all going to die enyway😂
does this show all colours of PH?
Same pigment found in red cabbage.
What's the price of this watch??
How difficult to carry out electrolysis on (NaOH)?
From what iv seen people heat the NaOH to boiling point (i think its roughtly 320c) and then apply current to it, sodium metal then forms. Im not sure if thier are any solvents/ electrolytes that can be used to avoid heating the NaOH however you would have no luck with water as the sodium ions would just react with the H2O to reform NaOH, this does however make NaOH a good electrolyte to use if your just trying to make oxygen and hydrogen as it is regenerative and doesn't release toxic gas like table salt!
❤ Amazing..... Awesome guys...
Super
Amazing!
why graphite electrode ?
Because graphite is a good conductor of electricity cause each carbon has 3 bonds and carbon has four electrons on its outer shell. As only 3 electrons are shared one is free. That's why it's being used.
Me coming here after Watching Dr, Stone😅
Us movement
Pow: you are making a minibomb without realizing it
Output wattage kitni hai?
Does Positive side hydrochloric acid?
Nope
1kg of caustic soda is like 4€ though, and much less work
Guess I'll just go buy some do i can make my damn soap
I certainly won't be able to do THIS, correctly...
Great guys I loved it! Thank you
Can we use different flowers
But green shows that it's neutral
What is the supplied Voltage
They used a USB plug so it would be 5V DC @ either .5amps or .9amps
Burning wood is literally making ash and some green house gas
I tried the same experiment and tested presence of sodium hydroxide with aluminum foil nothing happened
And me did it but nothing happened
You need to boil it at 75° celsius to evaporate water from it to make lye more concentrated. Measure its ph until it reaches 13 or 14
Can we use this naoh for saponification
If you intend to use it for soap I don't see why not if your doing it just becuase you can. the byproducts should all be non toxic apart from hypochlorite that forms from the chlorine, however I think this is a very low amount and is just essentially bleech and while toxic I doubt it will cause harm at this conceneration and would likely react with products in the soap anyway (wouldn't likely really be that toxic unless inhaled or injested even at higher concentrations), the rest of the chlorine should leave the solution as it is gaseous, same with the hydrogen and oxygen that are formed (though not toxic). The only remaining product that could be found would be the starting product NaCl, or table salt, which is obviously not toxic. DO HOWEVER BE VERY VERY CAREFUL WITH WHICH ELECTRODES YOU USE, iron will not last long as it will rapidly rust and leech into the solution, DO NOT BE TEMPTED TO USE STAINLESS STEAL EVER, stainless steel has chromium in it and can easily form hexavalent chromium, an extremely TOXIC and CARCINOGENIC (causes cancer) substance. Some however claim it to be safe for electrolysis of NaOH, but do you really want to take the risk with such a toxic substance? General rule of thumb is dont fuck with chromium unless you really know what you are doing, most labs wouldn't even fuck with some forms of chromium unless they have no other choice! Good electrodes tend to be very expensive like platinum however you can use carbon rods in a pinch but they wont be very good! With sodium hydroxide being very cheap I would suggest you just buy some in bulk (you can get it for under $15-20 a KG with it getting cheaper and cheaper the more you buy) im fairly sure you don't need that much for making soap anyway, I doubt you would save that much money away after factoring in the cost of electricity, even if you exlude the inital costs of the equipment. And you dont risk any exposure to chlorides that could form :)
We need to give the electricity for how many hours...??
You have to give electricity Until there is salt in the bottle
Jesus Christ our Lord and Savior is coming very soon. Please repent and preach the Gospel before it's too late. God bless you all. John 3:16 For God so loved the world, that He gave His only begotten Son, that whosoever believeth in Him should not perish, but have everlasting life. 1 John 5:12 Whoever has the Son has life; whoever does not have the Son of God does not have life. John 8:36 So if the Son sets you free, you will be free indeed. Romans 3:23 For all have sinned and fall short of the glory of God Romans 6:23 NLT “For the wages of sin is death, but the free gift of God is eternal life through Christ Jesus our Lord.” Matthew 11:15 Whoever has ears, let them hear. Revelation 22:12 And, behold, I come quickly; and my reward is with me, to give every man according as his work shall be. Romans 8:28 And we know that in all things God works for the good of those who love Him, who have been called according to His purpose
What is the name of paper that you r using
Thnx
Awesome experiment and explaination
What did you put the usb in? In a computer?
Fake
Water : salt ratio?
Depends upon the concentration of water or salt...
Chemical reaction formula?
GV?
Sir calculation
In case you are wondering, in order to convert the sodium hydroxide liquid into a powder, you have to boil the water until all you are left with is lye.
Bro you just made hcl and naclo
1000th like awesome channel
Great..!!
Bro super
Fake. Nathi. Ne
Did you make it in alcohol?