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CR-Scientific


Lead Acetate - Lab Notes


WARNING!  Soluble lead compounds are toxic.
If you choose to attempt this or any of the procedures described on this site, you do so entirely at your own risk.  In order to use this web site and/or any information contained herein, you must read and agree to the Terms of Use.


Lead acetate [Pb(CH3COO)2], or "salt of Saturn" as alchemists and early chemists called it, finds use in qualitative chemical analysis and also in the manufacture of other lead compounds, such as litharge (PbO;  used in assaying and refining silver and gold).  Lead acetate forms colored complexes with some of the anthocyanin pigments (for example, see http://www.crscientific.com/newsletter-10.html), as well as producing colorful chromates, antimonates, iodides, and other compounds.  It is very useful in the laboratory.

Lead acetate crystals
Figure 1.  Colorless crystals of lead acetate.  A concentrated Pb(OAc)2 solution became syrupy when heat-evaporated down to a fraction of its volume.  To avoid the possibility of complete solidification upon cooling, some dilute, aqueous Pb(OAc)2 was added.  The resulting solution was allowed to cool to room temperature, yielding the crystals shown above.

While irrational fear is counter-productive, it's important to avoid being cavalier with soluble lead compounds.   Though lead salts are not as toxic as their mercury counterparts, ingestion, inhalation, or skin absorption can still cause death or neurological and physiological damage.  Lead acetate is absorbed through skin.  Vinyl, latex, or nitrile gloves should be worn when handling the compound or its solutions.  If lead acetate contacts bare skin, it should be washed off immediately with water.  


Figure 2. Pb metal often contains appreciable amounts of Sn and Sb. These form insoluble compounds (e.g., SnO2xH2O) when treated with certain acids, especially under oxidizing conditions.  A traditional means of separating Pb, Sn, and Sb involves concentrated HNO3;  the Pb stays in solution as lead nitrate.



  Figure 3.  Crystals of lead acetate on a microscope slide.
Magnification ca. 40x.  Macroscopically, crystals of this
compound are almost colorless, acquiring a slight beige
tint if basic lead carbonate (etc) is present.

 
Lead acetate (or sometimes, lead nitrate) is used to make "sulfide test paper".  The presence of H2S causes the moistened paper to turn black;  the aqueous Pb2+ ions react with S2- to form the black, insoluble PbS.  This is a very sensitive test.  Decades ago, when lead paint was in common use, white-painted houses sometimes displayed the same effect;  white siding slowly turned black due to atmospheric H2S.  
Pb(OAc)2 , upon exposure to atmospheric CO2, becomes partially insoluble (Merck Index, 10th Edition, entries for "lead acetate" and "lead subacetate").  It tends to acquire an ivory or off-white tinge in the process.
Efflorescent compounds (including lead acetate) can be messy to crystallize by simple evaporation, since concentrated solutions tend to creep up the sides of the container.  This can leave crystal growths on the edges, on the rim, and even on the surrounding bench top.  It seems that the growing crystals have a wick-like effect on the mother liquor, drawing it up the walls of the crystallizing dish.


Figure 4. In experiments with other compounds, we have noted
that certain ones "climb" up the walls of the crystallizing dish as
the mother liquor evaporates.  This property was also observed
when trying to crystallize lead acetate by complete evaporation at
room temperature.  The results are shown in the photograph. 

It probably didn't help that seed crystals were not used.  There
were no nucleation points in the center of the dish, so the big
crystals accumulated near the edges.


Nearly all the carbonates, acetates, oxides, and hydroxides of lead are converted to PbO upon heating above 500°C, though Pb3O4 ("red lead") is typically an intermediate stage, especially if there is much air access to the sample and the heating is applied for a long time.  Lead chloride, however, remains chemically unchanged.  Oxychlorides, where present, tend to decompose back into PbCl2 and PbO on strong heating.  PbCl2 boils around 950°C (presenting a toxic inhalation hazard), though some will of course vaporize at lower temperatures (ventilation required!). 
Many lead compounds are reducible to Pb metal by roasting in the presence of charcoal in a reducing flame.  The laboratory must be ventilated well when performing such operations.  Even PbO can volatilize appreciably if heated strongly enough.
Containers that have been used to hold lead compounds or solutions should be presumed to have some residue in them, even when they look empty.  The treatment and recycling of laboratory-scale Pb wastes may be the subject of a future article.




Again, a word of caution-- soluble lead salts are toxicLead compounds must be stored in a securely locked cabinet where children, animals, and untrained personnel cannot get to them.  They must be labeled conspicuously as to their toxicity.  
If planning to handle or work with lead compounds, please find and download the relevant material safety data sheets (MSDS).
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Legal Notice:   In order to use this website or any information contained herein, you must read and agree to the Terms of UseMalicious or negligent use,  handling, or disposal of toxic materials can invite criminal prosecution.



Works Cited:

Merck Index, 10th Edition.  Rahway, New Jersey: Merck and Company, Inc., 1983.




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