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Japanese nuclear reactor problems
[quote]But, as with any engineering project, you have to draw a line somewhere otherwise nothing wou ... |
16-3-2011 at 17:23
by: madscientist |
Reactions
You need to learn the material, not just ask others to do your homework for you. That's called [i]ch ... |
16-3-2011 at 07:32
by: madscientist |
Japanese nuclear reactor problems
ScienceHideout: when fuel rods are exposed, they begin to melt. When they are completely molten, it' ... |
15-3-2011 at 15:34
by: madscientist |
Japanese nuclear reactor problems
I think they're more concerned about a decrease in surface area at this point. Anything that joins t ... |
15-3-2011 at 14:12
by: madscientist |
Japanese nuclear reactor problems
And although as time goes on, the material becomes less fissile, the surface area decreases as the r ... |
15-3-2011 at 11:35
by: madscientist |
Japanese nuclear reactor problems
"Don't worry, the situation is under control," they said. Kaboom. "Oh, not much radiation leaking," ... |
14-3-2011 at 17:01
by: madscientist |
DMF substitute in Wacker oxidation?
Are you sure about this? A google search revealed that dimethylfumurate has been banned by the EU, b ... |
10-3-2011 at 07:22
by: madscientist |
DMF substitute in Wacker oxidation?
It should work. Even protic solvents such as t-BuOH have been used. But I would read a review paper ... |
9-3-2011 at 10:12
by: madscientist |
How to stabilize freshly prepared H2O2?
Phosphoric acid is a common stabilizer. But be careful your source is clean. It's frequently contami ... |
7-3-2011 at 13:00
by: madscientist |
Keeping OTC chemicals OTC and bringing back home chemistry
[quote]not so much synthesize, more like possess and preserve. I can concentrate and preserve and as ... |
7-3-2011 at 07:27
by: madscientist |
Trimethylsulfonium bromide and its use for the methylation of phenols
Great work Nicodem! It's nice to know we can methylate phenols in an amateur environment without dea ... |
6-3-2011 at 11:46
by: madscientist |
New Energetic Materials - Current Research
[i]Where are your references?[/i] Your source doesn't cite a single one! |
2-3-2011 at 18:53
by: madscientist |
Hydrazine
[quote]I believe he was banned last time for spewing inane procedures that he had pulled out of his ... |
2-3-2011 at 18:51
by: madscientist |
Security of reagent orders from chemical companies in this age of chemophobia, paranoia and the oppressive health and safety nan
[quote].I've taught classes of kids older than you.[/quote]
And plenty who taught your generation ... |
28-2-2011 at 23:09
by: madscientist |
Iso-Butyl Nitrite
Back on topic, please! |
25-2-2011 at 23:26
by: madscientist |
Protecting phenols in a grignard reaction
Benzyl ethers can be cleaved in other ways too - strong acids, oxidation to benzoate and removal wit ... |
23-2-2011 at 15:53
by: madscientist |
Preparation of elemental phosphorus
Perhaps I'm overlooking something obvious, but it seems the use of SiO<sub>2</sub> with ... |
18-2-2011 at 11:27
by: madscientist |
Amateur chemist set off explosion near my home
The Energetic Materials section is not going anywhere.
There may be no real point in making PETN. ... |
16-2-2011 at 13:17
by: madscientist |
priming mixture for loading percussion caps
Every other post in this thread mentions firearms. Weapons discussion is forbidden on Sciencemadness ... |
16-2-2011 at 10:56
by: madscientist |
Amateur chemist set off explosion near my home
The Energetics Materials section does have a lot of problem posts. Please use the "Report" button on ... |
16-2-2011 at 10:38
by: madscientist |
Strong acids
garage_chemist, here's an excerpt from the Sixth Edition of Cotton's Advanced Inorganic Chemistry (p ... |
15-2-2011 at 17:06
by: madscientist |
L-tryptophan decarboxylation
Esters react with amines to form amides - I would use a different solvent. |
15-2-2011 at 09:22
by: madscientist |
LED Dangers - Unbelievable Paranoia!
Attention: anyone who wants to argue about atmospheric sciences should take it elsewhere. |
13-2-2011 at 11:46
by: madscientist |
Hofmann degradation and Amide hydrolysis
Crap - I meant to say "With hydrolysis of amides..." Sorry!  |
12-2-2011 at 13:35
by: madscientist |
Hofmann degradation and Amide hydrolysis
With amides, deprotonation doesn't yield a reaction, hence it's unimportant. With the Hofmann rearra ... |
12-2-2011 at 12:27
by: madscientist |
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