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Sulfide Ion (S²⁻)

  • Page ID
    97285
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    Acid Equilibria

    Sulfide is a strong base, so solutions of sulfide in water are basic, due to hydrolysis. Sulfide solutions develop the characteristic rotten-egg odor of \(\ce{H2S}\) as a result of this hydrolysis.

    \[\ce{S2^{-}(aq) + H2O(l) <=> HS^{-}(aq) + OH^{-}(aq) } \nonumber \]

    with \(K_b = 8.3\) and

    \[\ce{H^{-}(aq) + H2O(l) <=> H2S(aq) + OH^{-}(aq)} \nonumber \]

    with \(K_b = 1 \times 10^{-7}\).

    Solubility

    Many sulfide salts are insoluble in acidic or basic solution:

    • Acidic: \(\ce{PbS}\), \(\ce{Bi2S3}\), \(\ce{CuS}\), \(\ce{CdS}\), \(\ce{HgS}\), \(\ce{As2S3}\), \(\ce{Sb2S3}\), \(\ce{SnS2}\)
    • Basic: \(\ce{CoS}\), \(\ce{FeS}\), \(\ce{MnS}\), \(\ce{NiS}\), \(\ce{ZnS}\)

    Those salts that are insoluble in acidic solution are also insoluble in basic solution.

    A common test for aqueous sulfide ion involves acidification to form \(\ce{H2S}\), then exposure to moistened lead acetate paper to form black \(\ce{PbS}\) on the paper:

    \[\ce{Pb(OAc)2 + H2S -> PbS + 2HOAc} \nonumber \]

    Oxidation-Reduction:

    \(\ce{S2^{-}}\) or \(\ce{H2S}\) can be oxidized to yellow elemental sulfur in a colloidal form with fairly mild oxidizing agents, including nitric acid.


    This page titled Sulfide Ion (S²⁻) is shared under a CC BY-NC-SA 4.0 license and was authored, remixed, and/or curated by James P. Birk.

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