Sciencemadness Discussion Board
Not logged in [Login ]
Go To Bottom

Printable Version  
Author: Subject: can this work??[ammonia related]
HenningBasse
Harmless
*




Posts: 12
Registered: 22-1-2007
Location: Earth\'s Bottom
Member Is Offline

Mood: XTC

[*] posted on 5-2-2007 at 20:07
can this work??[ammonia related]


so , i've setup a little lab with few glassware and reagents , and i wanna make ammonia solution (like NH4Cl or NH4OH) to make some qualitative analysis

so , here are my thoughts about my recent experiment

Urea + NaOH (6 molar or more) +H2O (potable water)--heat-on-baker-->NH3(g) + NH4+(l) + NH2COO- + H2O

strong ammonia odor was released

then i added some 6 M HCl , got some redish brown precipitate (i tought it was some like NH2COOH) , and a strong ammonia smell decantate...so i filtered it and got this "ammonia liquid" .....but maybe its mixed with some urea that wasn't reacted with OH....

can u help me about key reaction CO(NH2)2 + OH --->NH3 + NH2COOH?? it's the right and unique way??? please some analytical and inorganic chemists help me out!! thx anyway
View user's profile View All Posts By User This user has MSN Messenger
Ozone
International Hazard
*****




Posts: 1269
Registered: 28-7-2005
Location: Good Olde USA
Member Is Offline

Mood: Integrated

[*] posted on 5-2-2007 at 20:59


Welcome to Science Madness.

Please check the Search feature before posting; this can get you to what you want much faster. Since direct NH3 from urea and the reactions involved have not to my knowledge been addressed, I'll let you off the hook;).

Another thread dealing with ammonia generation/concentration is here:

http://www.sciencemadness.org/talk/viewthread.php?tid=7464#p...

I'll also add that NaOH + amino acid + heat (glutamine, for example) will also yield NH3 (see deamidation). A paper describing the original urea assay is attached.

Cheers,

O3

Attachment: Urea Assay_01.pdf (599kB)
This file has been downloaded 778 times





-Anyone who never made a mistake never tried anything new.
--Albert Einstein
View user's profile View All Posts By User
HenningBasse
Harmless
*




Posts: 12
Registered: 22-1-2007
Location: Earth\'s Bottom
Member Is Offline

Mood: XTC

[*] posted on 5-2-2007 at 22:11


i realized that there's no NH2COOH precipitate since at low pH , the amine is already protonated NH3+COOH , so its quite soluble in acidic solution

(damn , feel bad for pass out that fault)
View user's profile View All Posts By User This user has MSN Messenger
HenningBasse
Harmless
*




Posts: 12
Registered: 22-1-2007
Location: Earth\'s Bottom
Member Is Offline

Mood: XTC

[*] posted on 5-2-2007 at 22:13


ehh , yeah , sorry about that Ozone , but really im not a new user here , this is just a new account...but anyway i must entered to some "welcome" forum....:(
View user's profile View All Posts By User This user has MSN Messenger
HenningBasse
Harmless
*




Posts: 12
Registered: 22-1-2007
Location: Earth\'s Bottom
Member Is Offline

Mood: XTC

[*] posted on 5-2-2007 at 22:37


a more theoretical approach

View user's profile View All Posts By User This user has MSN Messenger
guy
National Hazard
****




Posts: 982
Registered: 14-4-2004
Location: California, USA
Member Is Offline

Mood: Catalytic!

[*] posted on 5-2-2007 at 22:54


Quote:
Originally posted by HenningBasse
a more theoretical approach

It should be NH2COO- + NH3

[Edited on 2/6/2007 by guy]




View user's profile View All Posts By User
HenningBasse
Harmless
*




Posts: 12
Registered: 22-1-2007
Location: Earth\'s Bottom
Member Is Offline

Mood: XTC

[*] posted on 5-2-2007 at 23:09


Quote:
Originally posted by guy
Quote:
Originally posted by HenningBasse
a more theoretical approach

It should be NH2COO- + NH3

[Edited on 2/6/2007 by guy]


yeah , that's right , just i did it quickly on chemdraw :P
View user's profile View All Posts By User This user has MSN Messenger

  Go To Top