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・ Sodium tetraphenylborate
・ Sodium tetrasulfide
・ Sodium tetrathionate
・ Sodium thioantimoniate
・ Sodium thiocyanate
・ Sodium thiopental
・ Sodium thiosulfate
・ Sodium triacetoxyborohydride
・ Sodium triethylborohydride
・ Sodium trifluoromethanesulfinate
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・ Sodium triphosphate
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・ Sodium cocoate
・ Sodium cyanate
Sodium cyanide
・ Sodium cyanoborohydride
・ Sodium cyclamate
・ Sodium cyclopentadienide
・ Sodium decavanadate
・ Sodium dehydroacetate
・ Sodium diacetate
・ Sodium dichloroisocyanurate
・ Sodium dichromate
・ Sodium diethyldithiocarbamate
・ Sodium dihydrogen arsenate
・ Sodium dithionate
・ Sodium dithionite
・ Sodium dithiophosphate
・ Sodium diuranate


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Sodium cyanide : ウィキペディア英語版
Sodium cyanide

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Sodium cyanide is an inorganic compound with the formula NaCN. It is a white, water-soluble solid. Cyanide has a high affinity for metals, which leads to the high toxicity of this salt. Its main application, in gold mining, also exploits its high reactivity toward metals. When it is treated with acid, it forms the toxic gas hydrogen cyanide:
: NaCN + H2SO4 → HCN + NaHSO4
==Production and chemical properties==
Sodium cyanide is produced by treating hydrogen cyanide with sodium hydroxide:〔Andreas Rubo, Raf Kellens, Jay Reddy, Norbert Steier, Wolfgang Hasenpusch "Alkali Metal Cyanides" in Ullmann's Encyclopedia of Industrial Chemistry 2006 Wiley-VCH, Weinheim, Germany. 〕
:HCN + NaOH → NaCN + H2O
Worldwide production was estimated at 500,000 tons in the year 2006. Formerly it was prepared by the Castner-Kellner process involving the reaction of sodium amide with carbon at elevated temperatures.
: NaNH2 + C → NaCN + H2
The structure of solid NaCN is related to that of sodium chloride.〔Wells, A.F. (1984) Structural Inorganic Chemistry, Oxford: Clarendon Press. ISBN 0-19-855370-6.〕 The anions and cations are each six-coordinate. Potassium cyanide (KCN) adopts a similar structure. Each Na+ forms pi-bonds to two CN groups as well as two "bent" Na---CN and two "bent" Na---NC links.
Because the salt is derived from a weak acid, NaCN readily reverts to HCN by hydrolysis: the moist solid emits small amounts of hydrogen cyanide, which smells like bitter almonds (not everyone can smell it—the ability thereof is due to a genetic trait). Sodium cyanide reacts rapidly with strong acids to release hydrogen cyanide. This dangerous process represents a significant risk associated with cyanide salts. It is detoxified most efficiently with hydrogen peroxide (H2O2) to produce sodium cyanate (NaOCN) and water:〔
:NaCN + H2O2 → NaOCN + H2O

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