I need it for this bleachTry, oh, Amazon,, B&H, Adorama, ebay ....
It's pretty nasty stuff - out of curiosity, what's the intended use?
And why do you want this particular bleach?
Yeah, I am going to try to make RGB reflection holograms on Lippmann plates. I have had two from @amphetadreamer / jonhilty.com that I will be using.I take it you are experimenting with holography?
I would be lying if I pretended I knew what you're saying.Its mentioned as the best holographic bleach for reflection holograms out there. Others seem a lot more dangerous, like mercuric chloride? I dont know any other alternatives for reflection hologram processing
Yeah I figured that out and now I am just going to use EDTA bleach. I hope it works.You are aware of the safety hazards with PBQ and have access to appropriate measures to deal with them?
Since I could not order from Thermo Scientific, I found photographers formulary sells what I need and will get it to me as long as I do that DEA form. 10 measly grams is enough for 5 plates. The amount of potassium bromide used is also outrageous for a one time use bleach.
In the meantime, I am going to try to synthesize it with hydrogen peroxide and alcohol with hydroquinone. Any suggestions on how?
I see it done with bromate, sulfuric acid or potassium dichromate, and hydroquinone. I dont have the first two ingredients tho.
Keep in mind that quinone and its preparation are dangerous not only because of the caustic nature of the reagents, but the relatively high vapor pressure of PBQ and its relatively higher toxicity. I wouldn't attempt synthesizing it without proper equipment and safety gear.
If you go that route, I suggest you prepare it in situ rather than trying to isolate and purify the product. This could possibly be done by mixing HQ (MW 110g/mol, PBQ MW 108g/mol) and citric acid and adding hydrogen peroxide in 10-40% molar excess to the HQ (3% H2O2 is about 0.8-0.9 mol/L). The reaction should progress at room temp, but it might require gentle heating (up to 50C, otherwise you risk volatilizing and steam distilling the benzoquinone out of solution). Typically the reaction is carried out in acid medium,so the citric acid satisfies that requirement. Do not add the KBr before the reaction is complete or you will produce molecular bromine! That said, halogen salts are used as catalysts in the oxidation of aromatics, so a small amount (5-10% of the HQ mass) of the bromide could be added to facilitate the conversion. Expect a small amount of oxidized junk, the reaction goes through an intermediate quinhydrone, which might precipitate as green-brown needles.
Green has terrible spread, why is it oriented horizontal?
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