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Author: Subject: NHN synthesis not working
B(a)P
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[*] posted on 31-7-2023 at 17:13


Quote: Originally posted by ManyInterests  
Quote: Originally posted by B(a)P  
I recently saw this on youtube.
https://www.youtube.com/watch?v=enJAVGGTPQ4
Interestingly they use hydrazine sulfate directly (using sodium hydroxide to generate the hydrazine in the solution) with nickel nitrate. I have not tested this approach myself, curious if anyone else has though?


That's how I've been doing it all the time. He used Isopropyl alcohol while I used ethanol. It is possible to use methanol as well, but ethanol has the best yields.

When I freebase my hydrazine sulfate with sodium hydroxide and ethanol, I also need to filter out whatever solids that are left behind (my process for hydrazsulfate always has a little sodium sulfate in it). One thing that he is doing that I must do next is add nickel nitrate until I get that excess added and used up all my hydrazine freebase. since I didn't know you could do that (and easily get rid of the surplus, since NHN is water insoluble).


Where did they say they used isopropyl alcohol to liberate hydrazine? My understanding was they dissolved hydrazine sulfate in water then added sodium hydroxide to pH 8, heated the solution, then added the nickel nitrate solution. The isopropyl alcohol was used to wash the product.
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[*] posted on 31-7-2023 at 18:17


Quote: Originally posted by ManyInterests  
How fast does it burn? Does it instaneously vanish with a bright flash? Then that is probably good enough.

I need to make more NHN soon, since I am running out. The last time I made it, one of the batches I made seemed sub par. I wonder how well it would work as a cap on its own. I need to test them.


Here you can see the video..

Attachment: 20230801_073927~2.mp4 (4.7MB)
This file has been downloaded 155 times

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ManyInterests
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[*] posted on 31-7-2023 at 20:08


Quote:
Where did they say they used isopropyl alcohol to liberate hydrazine? My understanding was they dissolved hydrazine sulfate in water then added sodium hydroxide to pH 8, heated the solution, then added the nickel nitrate solution. The isopropyl alcohol was used to wash the product.


I stand corrected. I was confusing videos in my mind with one where Chemplayer freebases hydrazine with IPA and Ethanol in two separate attempts.

I did remember that Raid said he did liberate it with just water. I might do that next time if it is easier. Just keeping in mind that the pH needs to be 8 or thereabouts. I'm probably going to continue to use the old ethanol method since it worked for me quite a few times.

Quote:
Here you can see the video..

Attachment: 20230801_073927~2.mp4 (4.7MB)
This file has been downloaded 3 times


I always lit my NHN from the top and not the bottom, but that is some slow burning stuff. I think there is something wrong with it, but sadly I cannot tell what... :\
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[*] posted on 6-4-2024 at 18:28


I need to bump this thread back up due to a series of rather... irritating events. I wanted to make more NHN and since I had been quite experienced in making it and seen numerous setbacks and know how to deal with them, but my last two synthesis, especially my latest, has been a failure and I really don't understand why.

So here are the number of reagents used:

Hydrazine sulfate: 43.25g
95% ethanol: 150ml
sodium hydroxide: 26.4g

I had freebased my hydrazine the same way as I done before. Added the ethanol to the sulfate, mixed it thoroughly, then added the sodium hydroxide (I did it in one fell swoop). Everything was put in the fridge for days so it was ice cold to begin with, and I did it while everything was in an ice bath to keep things cool. The temperature never rose above 9C the whole time.

I mixed in a covered beaker and allowed it to settle, then mixed and such for 35 minutes to allow all the hydrazine to freebase. Then I filtered off the sulfate into a flask and heated it up (also covered) with strong stirring. I need to mention that the heating on my mantle is a bit unpredictable. When it was reaching the 60C the temperature then almost immediately shot up to 75C. Also since I was doing this on a windy day on my balcony, my flask tipped as well, it loosed up the plastic wrap that I was using to seal it and I saw fumes come out (no inhalation, I am fine). But when I added the nickel nitrate solution (I added more water to it, but it is still very emerald green, as pictured).

I am really confused as to what is happening here. My last attempt worked, but it yielded barely 4g. The last successful time I made it was in 2022 and I made two attempts that yielded 11.4g (of excellent quality NHN) and of 15.5g (of poor quality NHN that I had to get rid of) respectively. All other previous successful synthesis of mine also yielded much higher amounts of high quality NHN.

The first times I attempted they failed due to my hydrazine synthesis not working. But when I made the hydrazine sulfate for this they absolutely WERE hydrazine. I am really baffled.

Any thoughts? Any help?

Edit: Maybe I freebased my hydrazine wrong and it was destroyed by the temperature spike?

Edit2: when I added the nickel nitrate to the hydrazine solution It didn't turn torquoise blue. It remained green. Normally in a successful synthesis it would be immediately purple.

Edit3: upon further thing, this probably is a hydrazine issue. Either the original synthesis, or I was too cavalier with the freebasing.

IMG_20240406_222009100 - Copy.jpg - 1.7MB

[Edited on 7-4-2024 by ManyInterests]

[Edited on 7-4-2024 by ManyInterests]

[Edited on 7-4-2024 by ManyInterests]
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[*] posted on 6-4-2024 at 20:53


Are you sure the free-basing reaction took place at all? If your reagents are dry and cold enough, the reaction may not start. What’s your source of hydrazine sulfate and nickel nitrate?



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[*] posted on 7-4-2024 at 04:49


Quote: Originally posted by Sir_Gawain  
Are you sure the free-basing reaction took place at all? If your reagents are dry and cold enough, the reaction may not start. What’s your source of hydrazine sulfate and nickel nitrate?


That could be my problem. It could have been too cold. All regents were very cold except for the nickel nitrate solution, it was at room temperature.

The Hydrazine sulfate I made myself with the Hoffman rearrangement of urea. The nickel nitrate was purchased from a chemical supplier online. It was Nickel(II)nitrate hexahydrate.

I had successfully made hydrazine sulfate many times before and they all made NHN. At this point I will believe that you are right. No freebasing occurred because everything was too cold.

Edit: This is one aspect that I as unaware would happen. I had no idea that that freebasing needs some decent temperature. I remember being warned that it can get hot and you can lose your hydrazine, I didn't store ingredients in the fridge previously, I think this was the mistake I made this time. Not my nickel nitrate solution being too concentrated or maybe even the temperature spike on the mantle.

[Edited on 7-4-2024 by ManyInterests]
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