In this video we show how to make a dye sensitized solar cell based on titanium dioxide and anthocyanin found in raspberries.
First get some titanium dioxide (anatase structure), about 0.5g will do. Then mix it with drops of vinegar until it has the consistency of thin paint or liquid corrector fluid. Add a drop of dishwashing detergent. This is to make it stick to the glass.
Now get a piece of indium tin oxide glass. The indium tin oxide glass was purchased from delta technologies http://www.delta-technologies.com/
using a multimeter set to measure resistance, find the conductive side by measuring the resistance of the glass. The side that's conductive will have a much lower resistance than the non-conductive side.
Tape the glass on three sides onto a flat surface, conductive side up. there should be able 5mm of tape on each edge. The tape will serve as a spacer guide for the titanium dioxide.
In this video we make a sodium oxalate, a simple primary standard for the standardization of potassium permanganate titrant.
The reaction is pretty simple. 120g of oxalic acid is dissolved in 300mL of boiling water and mixed with 80g of sodium hydroxide dissolved in 200mL of water. The sodium oxalate precipitates out and is allowed to cool. It is filtered and dried.
Sodium oxalate will be used in an upcoming video to standardize potassium permanganate solution that will in turn be used to titrate hydrogen peroxide.
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https://www.youtube.com/watch?v=227KdtAK1yU
An improved method to make "Hot Ice" sodium acetate from vinegar and baking soda.
Boiling down the sodium acetate solution to exactly the right level is key to making sodium acetate work. Since most of you don't have precise glassware like I do, you can follow this new method of boiling to get the concentration just right.
Simply make a raw sodium acetate solution like in our previous video at this link: http://www.youtube.com/watch?v=jpEZWdPIg9o
But instead of boiling down 90%, just watch the surface of the boiling liquid.
As you pass the key concentration for making hot ice, a crust of sodium acetate will start to form on the surface. As soon as you see this crust take it off heating. While it is still hot, stir the mixture and add a small amount of water, usually just a spoonful or so, to redissolve the crust.
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In this video we make copper formate, a useful precursor to copper conductive ink.
We simply dissolve 65g of copper sulfate in 250mL of water and 33g of sodium carbonate in 150mL of water. Then we mix the two together. Copper carbonate hydroxide precipitates and we filter that off. Then we react the copper carbonate hydroxide with formic acid to create copper formate.
Copper formate has the useful property that it decomposes into copper metal (along with carbon dioxide and hydrogen) when heated. The copper produced this way isn't well bonded and not very conductive. But in upcoming videos additives may be added to improve the quality of the product.
Related videos:
Silver conductive ink: https://www.youtube.com/watch?v=EBlqPS8boLI
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https://www.youtube.com/watch?v=auyCK8-DMP0
In this video we react brake fluid with potassium chlorate.
Related videos:
Previous video: https://www.youtube.com/watch?v=Enf76lBNUIY
Making potassium chlorate from bleach: https://www.youtube.com/watch?v=JtxQT7aVDeg
Chemists lights a barbecue with potassium chlorate:
https://www.youtube.com/watch?v=eRtaPlEcEUU
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https://www.youtube.com/watch?v=CgBWnDTcE2o
Make Potassium Nitrate from Instant Cold Packs and Potassium Hydroxide
Warning: This reaction will produce large quantities of toxic ammonia gas. Perform the reaction outside or in a fume hood. Potassium hydroxide is highly corrosive; wear gloves when working with it.
Also note that this video is for those interested in the chemistry, it's not cheaper/better/easier than buying it.
Take 60g of potassium hydroxide and combine it with 80g of ammonium nitrate. We showed how to obtain ammonium nitrate from instant cold packs in a previous video. Potassium hydroxide is sold online to make homemade soaps and for biodiesel.
Now add 30ml of water and gently heat the mixture. It will first bubble as it releases ammonia gas and then continue heating until it boils. Let it cool and evaporate to dryness.
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https://www.youtube.com/watch?v=XxhZkDAOeQ8
In this video we discuss the idea behind the short path distillation apparatus.
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In this video we make silver powder using electrochemistry.
The process is pretty simple. Make a solution of 1g silver nitrate in 50mL water. Submerge an anode made of pure silver (i'm using silver coins) and a cathode of carbon. Connect the anode (silver) to the positive terminal of a variable power supply and connect the cathode (carbon) to the negative terminal. Apply a current and raise it until the cathode just starts to bubble hydrogen and then lower it about 25%. Magnetic stirring and a stir bar should be applied to constantly shred the silver dendrites as they grow.
Eventually the anode will be consumed and the solution is decanted to recover the silver powder. The silver powder is washed a few times with water and then dried by heating on the hot plate.
Related videos:
Restoring Silver by electrochemistry: https://www.youtube.com/watch?v=57iwtmT4LNQ
Toning Silver by Anodization : https://www.youtube.com/watch?v=GajkqaSr01c
Make zinc powder: https://www.youtube.com/watch?v=3X9c6epL7HQ
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In this video we make luminol from domestically available chemicals.
The process pretty complicated and dangerous at parts and so should only performed by, or under the direct supervision of, an experienced chemist.
First we obtain diethylhexyl phthalate by refluxing 50g of finely cut vinyl gloves in enough isopropanol to completely cover them for at least one hour, preferably three to four.
The alcohol solution of diethylhexyl phthalate is filtered and the supernatant is boiled until it reduces to half its volume. An equal amount of water along with 10g of sodium hydroxide is added and the mixture boiled for an hour. This causes the diethylhexyl phthalate to hydrolyze into phthalic acid and 2-ethylhexanol. After the solution cools it will phase separate into an aqueous layer containing disodium phthalate and an organic layer containing the alcohols.
Retaining just the aqueous layer, 25mL of 12 molar hydrochloric acid is added to precipitate the phthalic acid. Chilling may be necessary. The supernatant is discarded and the residue of wet phthalic acid is purified and converted into phthalic anhydride by heating it to 300 Celsius. First the water boils off and then the phthalic anhydride evaporates and condenses on the sides of the beaker. At this point a flask of cold water is placed over the beaker to allow the phthalic anhydride to deposit on it. Periodically the phthalic anhydride deposits are harvested until no more can be obtained.
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https://www.youtube.com/watch?v=58Ve69s0qD0
In this video we get Guanidine Carbonate and Hydrochloride from no-lye hair relaxants
Related videos:
Aspirator vacuum pump: https://www.youtube.com/watch?v=tYLlkTDstmo
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