Sulfur-nitrogen compounds hydrogen sulfide

Direct conversion of target compounds (sulfur and nitrogen compounds, hydrogen sulfide, polyaromatics, etc.) to an easily removable or desirable product. 

The influence of these inhibitors is known to increase in the following order saturated hydrocarbons, monoaromatics < condensed aromatics, oxygen compounds, hydrogen sulfide < organic sulfur compounds < basic nitrogen compounds. Three of these inhibitor classes are discussed here. 

The problem of the synthesis of highly substituted olefins from ketones according to this principle was solved by D.H.R. Barton. The ketones are first connected to azines by hydrazine and secondly treated with hydrogen sulfide to yield 1,3,4-thiadiazolidines. In this heterocycle the substituents of the prospective olefin are too far from each other to produce problems. Mild oxidation of the hydrazine nitrogens produces d -l,3,4-thiadiazolines. The decisive step of carbon-carbon bond formation is achieved in a thermal reaction a nitrogen molecule is cleaved off and the biradical formed recombines immediately since its two reactive centers are hold together by the sulfur atom. The thiirane (episulfide) can be finally desulfurized by phosphines or phosphites, and the desired olefin is formed. With very large substituents the 1,3,4-thiadiazolidines do not form with hydrazine. In such cases, however, direct thiadiazoline formation from thiones and diazo compounds is often possible, or a thermal reaction between alkylideneazinophosphoranes and thiones may be successful (D.H.R. Barton, 1972, 1974, 1975). 

Lead dioxide Aluminum carbide, hydrogen peroxide, hydrogen sulfide, hydroxylamine, ni-troalkanes, nitrogen compounds, nonmetal halides, peroxoformic acid, phosphorus, phosphorus trichloride, potassium, sulfur, sulfur dioxide, sulfides, tungsten, zirconium... 

Sulfurization of unsaturated compounds and meicaptans is normally carried out at atmospheric pressure, in a mild or stainless steel, batch-reaction vessel equipped with an overhead condenser, nitrogen atmosphere, an agitator, heating media capable of 120—215°C temperatures and a scmbber (typically caustic bleach or diethanolamine) capable of handling hydrogen sulfide. If the reaction iavolves the use of H2S as a reactant or the olefin or mercaptan is a low boiling material, a stainless steel pressurized vessel is recommended. 

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 ... 

Raw material input to petroleum refineries is primarily crude oil however, petroleum refineries use and generate an enormous number of chemicals, many of which leave the facilities as discharges of air emissions, wastewater, or solid waste. Pollutants generated typically include VOCs, carbon monoxide (CO), sulfur oxides (SOJ, nitrogen oxides (NOJ, particulates, ammonia (NH3), hydrogen sulfide (HjS) metals, spent acids, and numerous toxic organic compounds. 

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... 

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