Open main menu
Home
Random
Recent changes
Special pages
Community portal
Preferences
About Wikipedia
Disclaimers
Incubator escapee wiki
Search
User menu
Talk
Dark mode
Contributions
Create account
Log in
Editing
Lead(II) nitrate
(section)
Warning:
You are not logged in. Your IP address will be publicly visible if you make any edits. If you
log in
or
create an account
, your edits will be attributed to your username, along with other benefits.
Anti-spam check. Do
not
fill this in!
== Applications == Lead nitrate has been used as a heat stabiliser in nylon and polyesters, as a coating for [[thermography|photothermographic]] paper, and in [[rodenticide]]s.<ref name="greenwood"/> Heating lead nitrate is convenient means of making [[nitrogen dioxide]]: :<chem>2 Pb(NO_3)_2->[\Delta]2PbO + 4NO_2 +O_2 </chem> In the [[gold cyanidation]] process, addition of lead(II) nitrate solution improves the [[Tank leaching|leaching]] process. Only limited amounts (10 to 100 milligrams lead nitrate per kilogram gold) are required.<ref>{{cite journal|first = Fathi|last = Habashi|title = Recent advances in gold metallurgy|year = 1998 |journal=Revisa de la Facultad de Ingeniera, Universidad Central de Venezuela|volume=13|issue=2|pages=43β54}}</ref><ref>{{cite web|url = http://www.e-goldprospecting.com/html/auxiliary_agents_in_gold_cyani.html|title = Auxiliary agents in gold cyanidation|publisher = Gold Prospecting and Gold Mining|access-date = 2008-01-05}}</ref> In organic chemistry, it may be used in the preparation of [[isothiocyanate]]s from [[dithiocarbamate]]s.<ref name="OrgSynDains">{{OrgSynth|author =Dains, F. B.|author2 =Brewster, R. Q.|author3 =Olander, C. P. |title = Phenyl isothiocyanate|collvol = 1|collvolpages = 447|prep = cv1p0447}}</ref> Its use as a [[bromide]] scavenger during [[SN1 reaction|S<sub>N</sub>1 substitution]] has been reported.<ref name="OrgSynRapoport"> {{OrgSynth|author = Rapoport, H.|author2 = Jamison, T.|collvol = 9|collvolpages = 344|prep = cv9p0344|year = 1998|title = (S)-N-(9-Phenylfluoren-9-yl)alanine and (S)-Dimethyl-N-(9-phenylfluoren-9-yl)aspartate}}</ref>
Edit summary
(Briefly describe your changes)
By publishing changes, you agree to the
Terms of Use
, and you irrevocably agree to release your contribution under the
CC BY-SA 4.0 License
and the
GFDL
. You agree that a hyperlink or URL is sufficient attribution under the Creative Commons license.
Cancel
Editing help
(opens in new window)