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Sodium hydrosulfide is the chemical compound with the formula NaHS. This compound is the product of the half -neutralization of hydrogen sulfide with a sodium-derived base. NaHS is a useful reagent for the synthesis of organic and inorganic sulfur compounds. It is a colorless solid that typically smells like H2S due to hydrolysis by atmospheric moisture. In contrast with Na2S, which is insoluble in organic solvents, NaHS, being a 1:1 electrolyte, is more soluble. Alternatively, in place of NaHS, H2S can be treated with an organic amine to generate an ammonium salt. Solutions of SH- are sensitive to oxygen, converting mainly to polysulfides, indicated by the appearance of yellow.
[edit] Structure and propertiesCrystalline NaHS undergoes two phase transitions. At temperatures above 360K, NaHS adopts the NaCl structure, which implies that the HS- behaves as a spherical anion due to its rapid rotation leading to equal occupancy of eight equivalent positions. Below 360K, a rhombohedral structure forms, and the HS- sweeps out a discoidal shape. Below 114K, the structure becomes monoclinic. The analogous rubidium and potassium compounds behave similarly.[1] NaHS has a relatively low melting point of 350 °C. In addition to the aforementioned anhydrous forms, it can be obtained as two different hydrates, NaHS.2H2O and NaHS.3H2O. These three species are all colorless and behave similarly, but not identically. [edit] PreparationThe usual laboratory synthesis entails treatment of NaOMe with hydrogen sulfide:[2]
Industrially, NaOH is employed as the base. The quality of the NaHS can be assayed by iodometric titration, exploiting the ability of HS– to reduce I2. [edit] ApplicationsThousands of tons of NaHS are produced annually. Its main uses are in paper manufacture as a makeup chemical for sulfur used in the Kraft process, as a flotation agent in copper mining where it is used to activate oxide mineral species, and in the leather industry for the removal of hair from hides. [edit] References
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