Hydrogen cyanide sulfide

Compounds with active hydrogen add to the carbonyl group of acetone, often followed by the condensation of another molecule of the addend or loss of water. Hydrogen sulfide forms hexamethyl-l,3,5-trithiane probably through the transitory intermediate thioacetone which readily trimerizes. Hydrogen cyanide forms acetone cyanohydrin [75-86-5] (CH2)2C(OH)CN, which is further processed to methacrylates. Ammonia and hydrogen cyanide give (CH2)2C(NH2)CN [19355-69-2] ix.orn. 6<55i the widely used polymerization initiator, azobisisobutyronitrile [78-67-1] is made (4). 

Health nd SMety Factors. The lowest pubhshed human oral toxic dose is 430 mg/kg, causing nervous system disturbances and gastrointestinal symptoms. The LD q (rat, oral) is 750 mg/kg (183). Thiocyanates are destroyed readily by soil bacteria and by biological treatment systems in which the organisms become acclimatized to thiocyanate. Pyrolysis products and combustion products can include toxic hydrogen cyanide, hydrogen sulfide, sulfur oxides, and nitrogen oxides. 

Himethylformamide [68-12-2] can be produced from the reaction of hydrogen cyanide and methanol. Adenine [73-24-5] can be prepared from hydrogen cyanide in Hquid ammonia. Thioformamide [115-08-2] can be produced from hydrogen cyanide and hydrogen sulfide. 

Emissions to the atmosphere from ammonia plants include sulfur dioxide (SOj), nitrogen oxides (NOJ, carbon monoxide (CO), carbon dioxide (COj), hydrogen sulfide (HjS), volatile organic compounds (VOCs), particulate matter, methane, hydrogen cyanide, and ammonia. The two primary sources of pollutants, with typical reported values, in kilograms per ton (kg/t) for the important pollutants, are as follows ... 

Carbon dioxide, carbonyl sulfide, hydrogen cyanide, propylene, and butadiene... 

Hydrogen cyanide (anhydrous), 15, 89 Hydrogen peroxide, 13, 94 16, 31 16, 4 Hydrogen sulfide, 16, 81 Hydrolysis... 

Seif-Test D.4B Write the formulas for (a) cesium sulfide tetrahydrate (b) manganese(VII) oxide (c) hydrogen cyanide (a poisonous gas) (d) disulfur dichloride. 

It is apparent that a new synthetic methodology, preferably catalytic, is needed for the synthesis of this important class of 2-(perfinoroalkyl)ethane thiols. In this context, a variety of catalysts was examined to determine if they wonld catalyze the hydrogenolysis of 2-(perfinorohexyl)ethane thiocyanate. In the conrse of this study, much to our surprise, it was discovered that a carbon supported Pd-Sn would catalyze the reaction. It is known that palladium and other group Vtll metal catalysts are poisoned by the product thiol, traces of hydrogen sulfide byproduct, and the hydrogen cyanide co-prodnct (6), but our observations are that this catalyst is surprisingly robust in the reaction medium. 

The thiol was obtained in >98% yield with trace amounts of the disulfide at 175°C and 700 psig H2 reactor pressnre in 1.5 honrs at a 900 1 substrate catalyst molar ratio. As discussed above, it is known that palladinm and other groups 8 to 10 metal catalysts are poisoned by the prodnct thiol, traces of hydrogen sulfide byproduct, and hydrogen cyanide coprodnct (6), bnt it is surprising that this catalyst is so robnst The effects of solvents, temperature, pressure, catalyst, and recycle will be discnssed. The characterization of the catalyst by various techniques will help to explain some of these observations. 

It is well known that palladium on carbon catalysts are poisoned by hydrogen cyanide and thiol products or hydrogen sulfide (6). Therefore, it was of interest to investigate the reduction of perfluoroalkyl thiocyanates as a function of tin concentration, keeping the concentration of palladium and reaction conditions constant. Figure 15.1 delineates the % conversion vs. Sn/Pd ratio, under the same reaction conditions of 175°C, 700 psig H2 for 2 hours with 5% Pd on carbon catalysts in ethyl acetate solvent at a 1000 1 substrate catalyst molar ratio. The increase in... 

In the blast furnace, the reaction of the nitrogen in the blast with coke leads to the formation of poisonous chemicals such as hydrogen cyanide and cyanogens, and each cubic meter of the blast furnace gas contains from 200 to 2000 mg of these compounds. The blast furnace gas is scrubbed with water in the dust collection system the cyanide compounds dissolve in the water, which is then discharged after the compounds have been destroyed. Another poisonous emission in blast furnace operations is hydrogen sulfide. The sulfur present in the coke is converted into calcium sulfide in the slag, the water-quenching of... 

DIAMOX A process for removing hydrogen sulfide and hydrogen cyanide from coke oven gas by absorption in aqueous ammonia. Developed by Mitsubishi Chemical Industries and Mitsubishi Kakoki Kaisha and operated in Japan. 

F-S [Ferrous sulfate] A process for removing ammonia, hydrogen sulfide, and hydrogen cyanide from coke-oven gas by scrubbing with aqueous ferrous sulfate solution obtained from steel pickling. A complex series of reactions in various parts of the absorption tower yield ammonium sulfate crystals and hydrogen sulfide (for conversion to sulfur or sulfuric acid) as the end products. Developed in Germany by F. J. Collin A.G. 

Fu maks-Rhodaks A combination of the Fumaks and Rhodaks processes for removing both hydrogen sulfide and hydrogen cyanide from coke-oven gas. Developed by the Osaka Gas Company and marketed by Sumitomo Chemical Engineering Company. 

Weedon, F.R, A.Hartzell, and C.Setterstrom. 1940. Toxicity of ammonia, chlorine, hydrogen cyanide, hydrogen sulfide and sulfur dioxide gases. V. Animals. Contrib. Boyce Thompson Inst. 11 365-385. 

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