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Newest chemical elements get proposed names
Hugenucleium is G1  |
3-1-2012 at 02:36
by: Adas |
Recovery of K2SO4 from K2SO4/H2SO4/HNO3
[rquote=231599&tid=18402&author=hissingnoise]Heating converts bisulphate to sulphate - small ... |
2-1-2012 at 05:32
by: Adas |
Recovery of K2SO4 from K2SO4/H2SO4/HNO3
Distill off the acids, crystals will stay. And they are probably (mostly) hydrogensulfates, not sulf ... |
2-1-2012 at 05:02
by: Adas |
Esterification Reaction
NaOH can easily eat through your glassware, I wouldn't do it. |
1-1-2012 at 03:36
by: Adas |
Have you told anyone about the forum?
I mentioned SM to 3 people I know very well, but none of them is really interested in this forum, be ... |
31-12-2011 at 16:38
by: Adas |
Esterification Reaction
These salts are pretty unreactive. Nothing to be worry about  |
31-12-2011 at 14:23
by: Adas |
Esterification Reaction
Just try to remove the reaction water using anhydrous salts (MgSO4, CaCl2...) - water removal is mos ... |
31-12-2011 at 13:42
by: Adas |
things to do with copper carbonate?
Thank you, bbartlog!  |
31-12-2011 at 06:51
by: Adas |
things to do with copper carbonate?
What about toxicity to humans? Because I am now a bit afraid to work with Cu compounds, as they migh ... |
31-12-2011 at 02:02
by: Adas |
Drying acetic acid
AFAIK, DCM [i]is[/i] flammable. And I think this may describe the greenish colour of the flame, but ... |
30-12-2011 at 13:13
by: Adas |
Maximum NaClO % from brine electrolysis
[rquote=231317&tid=18377&author=hissingnoise]You could always bubble chlorine into a cold hy ... |
29-12-2011 at 13:23
by: Adas |
Copper Citrate Production
1. Too slow.
2. I am not sure, just test it. |
29-12-2011 at 11:46
by: Adas |
Copper Citrate Production
Cu + H2O2 + citric acid, if you want to waste H2O2 :/
Purchasing some CuSO4 is far more economical. |
29-12-2011 at 10:36
by: Adas |
Copper Citrate Production
Start from copper sulfate:
CuSO4 + NaHCO3 ----> CuCO3 + CO2 + H2O
CuCO3 is insoluble, so wash ... |
29-12-2011 at 10:26
by: Adas |
Org Synth: Trymethylamine
Peach, why these complex procedures? The easiest thing is to make HCl salt, and when needed, release ... |
29-12-2011 at 09:30
by: Adas |
Amine Peroxides - the others
What about this one made of acetamide?
[img]http://img839.imageshack.us/img839/7427/peroxidacet ... |
29-12-2011 at 06:35
by: Adas |
Org Synth: Trymethylamine
[rquote=231269&tid=18366&author=Dr.Bob]Simplest would be excess ethyl iodide and ammonia in ... |
29-12-2011 at 06:15
by: Adas |
Exotic Primaries - Complex Salts
Formatik, please, upload your videos on MediaFire next time if you can. It is free and I must not wa ... |
29-12-2011 at 03:34
by: Adas |
NaOH + CH2O
I am sorry to bring up an old topic, but I want to ask what happens, if anhydrous CH2O and NaOH reac ... |
28-12-2011 at 05:52
by: Adas |
Is milk acidic or basic?
[rquote=231134&tid=18221&author=Formatik]I recently tested the pH of raw egg yolk and found ... |
28-12-2011 at 02:41
by: Adas |
New Energetic Materials - Current Research
Yesterday I got an idea of making biuret dioxime. I don't think it's impossible, but I can't find an ... |
27-12-2011 at 02:46
by: Adas |
Nitroglycerin discoloration
Have you tried neutralizing the NG with soda? |
26-12-2011 at 14:04
by: Adas |
Reaction between SO3 and nitrates
[rquote=230754&tid=18336&author=hissingnoise]Fixed it L-E . . . (Christmas spirit --- hic?)
... |
23-12-2011 at 12:26
by: Adas |
Reaction between SO3 and nitrates
[rquote=230734&tid=18336&author=hissingnoise]No is the short answer!
SO<sub>3</sub ... |
23-12-2011 at 09:57
by: Adas |
MgSO4 to sulfuric acid
[rquote=230738&tid=18333&author=Bot0nist]He reads, I suggest you do the same...
http://en.m ... |
23-12-2011 at 09:54
by: Adas |
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