Sodium ethyl xanthate (SEX)[1] is an organosulfur compound with the chemical formula . It is a pale yellow powder, which is usually obtained as the dihydrate. Sodium ethyl xanthate is used in the mining industry as a flotation agent.[2] A closely related potassium ethyl xanthate (KEX) is obtained as the anhydrous salt.
Akin to the preparation of most xanthates, sodium ethyl xanthate can be prepared by treating sodium ethoxide with carbon disulfide:[3]
Sodium ethyl xanthate is a pale yellow powder. Its aqueous solutions are stable at high pH if not heated. It rapidly hydrolyses at pH less than 9 at 25 °C. It is the conjugate base of the ethyl xanthic acid, a strong acid with pKa of 1.6 and pKb estimated as 12.4 for the conjugate base.[4] Sodium ethyl xanthate easily adsorbs on the surface of many sulfide minerals,[5] a key step in froth flotation.
Xanthates are susceptible to hydrolysis and oxidation[6] at low pH:
Oxidation gives diethyl dixanthogen disulfide:
Sodium ethyl xanthate can be identified through optical absorption peaks in the infrared (1179, 1160, 1115, 1085 cm−1) and ultraviolet (300 nm) ranges. There are at least six chemical detection methods:
Sodium ethyl xanthate can also be quantified using gravimetry, by weighing the lead xanthate residue obtained after reacting SEX with 10% solution of lead nitrate. There are also several electrochemical detection methods, which can be combined with some of the above chemical techniques.[8]
Sodium ethyl xanthate is used in the mining industry as flotation agent for recovery of metals, such as copper, nickel, silver or gold, as well as solid metal sulfides or oxides from ore slurries. This application was introduced by Cornelius H. Keller in 1925. Other applications include defoliant, herbicide, and an additive to rubber to protect it against oxygen and ozone.[9]
In 2000, Australia produced up to 10,000 tonnes of sodium ethyl xanthate and imported about 6,000 tonnes, mostly from China.[10] The material produced in Australia is the so-called 'liquid sodium ethyl xanthate' that refers to a 40% aqueous solution of the solid.[11] It is obtained by treating carbon disulfide with sodium hydroxide and ethanol. Its density is 1.2 g/cm3 and the freezing point is −6 °C.[12]
Sodium ethyl xanthate has moderate oral and dermal toxicity in animals and is irritating to eyes and skin.[13] It is especially toxic to aquatic life and therefore its disposal is strictly controlled.[14] Median lethal dose for (male albino mice, oral, 10% solution at pH~11) is 730 mg/kg of body weight, with most deaths occurring in the first day. The most affected organs were the central nervous system, liver and spleen.[15]
Since 1993, sodium ethyl xanthate is classified as a Priority Existing Chemical in Australia, meaning that its manufacture, handling, storage, use or disposal may result in adverse health or environment effects. This decision was justified by the widespread use of the chemical in industry and its decomposition to the toxic and flammable carbon disulfide gas. From two examples of sodium ethyl xanthate spillage in Australia, one resulted in evacuation of 100 people and hospitalization of 6 workers who were exposed to the fumes. In another accident, residents of the spillage area complained of headache, dizziness, and nausea.[16] Consequently, during high-risk sodium ethyl xanthate handling operations, workers are required by the Australian regulations to be equipped with protective clothing, anti-static gloves, boots and full-face respirators or self-contained breathing apparatus.[17]