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Potassium iron sulfide

Antimony trisulfide, carbon disulfide vapour, chromium(II) sulfide and hydrogen sulfide all ignite in contact with fluorine at ambient temperature, the solids becoming incandescent [1]. Iron(II) sulfide reacts violently on mild warming, and barium sulfide, potassium sulfide or zinc sulfide all incandesce in the gas, as does molybdenum(III) sulfide at 200°C [2],... [Pg.1520]

Iron (III), Fe 3 Ammonia solution Ammonium sulfide Potassium cyanide... [Pg.538]

Separate acids from incompatible materials such as bases, active metals (ex. sodium, magnesium, potassium) and from chemicals which can generate toxic gases when combined (ex. sodium cyanide and iron sulfide). [Pg.34]

Nearly all alkali metal compounds are soluble in water. Sulfide and phosphate compounds are usually insoluble. How, then, do you account for the fact that sodium sulfide and potassium phosphate are soluble, while iron sulfide and calcium phosphate are insoluble Why do some ions form soluble compounds, while other ions form insoluble compounds ... [Pg.330]

Ignition or explosive reaction with metals (e.g., aluminum, antimony powder, bismuth powder, brass, calcium powder, copper, germanium, iron, manganese, potassium, tin, vanadium powder). Reaction with some metals requires moist CI2 or heat. Ignites with diethyl zinc (on contact), polyisobutylene (at 130°), metal acetylides, metal carbides, metal hydrides (e.g., potassium hydride, sodium hydride, copper hydride), metal phosphides (e.g., copper(II) phosphide), methane + oxygen, hydrazine, hydroxylamine, calcium nitride, nonmetals (e.g., boron, active carbon, silicon, phosphoms), nonmetal hydrides (e.g., arsine, phosphine, silane), steel (above 200° or as low as 50° when impurities are present), sulfides (e.g., arsenic disulfide, boron trisulfide, mercuric sulfide), trialkyl boranes. [Pg.315]

Froth flotation is used to raise the low mineral concentrations in ores to concentrations that can be more economically processed. A concentration of 25-30% is suitable for economical smelting of copper. The froth flotation technique was originally developed in about 1910 to raise the copper concentrations of the strip-mined ores of Bingham Canyon, near Salt Lake City [9], and was further perfected for the differential separation of lead, zinc, and iron sulfides at Trail, B.C., at about the same time [10]. Flotation technologies are now widely used for separations such as the beneficiation of low grade Florida phosphate ores from 30-40% to 60-70% concentrations of calcium phosphate (BPL), and the separation of about 98% potassium chloride from sylvinite, a natural mixture of potassium and sodium chlorides. It is also used for bitumen separation from tar sand, removal of slate from coal, and removal of ink from repulped paper stock preparatory to the manufacture of recycled paper stock. More details of these separations are discussed in the relevant chapters. [Pg.395]

BROMURO de AZUFRE (Spanish) (13172-31-1) Combustible liquid. Reacts with moisture in air, steam, or oxidizers, emitting fumes of hydrogen bromide and sulfur dioxide. Reacts with water, forming hydrobromic acid and fumes of hydrogen bromide and sulfur dioxide. Violent reaction with strong oxidizers, chromyl chloride, diethylzinc, dimethyl sulfoxide, lead dioxide, nitric acid, potassium. Incompatible with hexafluoroisopropylide-neaminolithium, iron sulfide, nickel, red phosphorus. Attacks most metals in the presence of moisture. [Pg.204]

BUTENE OXIDE (106-88-7) Forms explosive mixture with air (flash point -7°F/-22°C). Unless inhibited, violent polymerization can be caused by elevated temperatures, sunlight, acids, aluminum chlorides, bases, iron, tin, potassium, sodium, sodium hydroxide, or certain salts. Reacts violently with oxidizers, alcohols. Reacts with hydroxides, metal chlorides, oxides. Flow or agitation of substance may generate electrostatic charges due to low conductivity. Storage tanks and other equipment should be absolutely dry and free from air, ammonia, acetylene, hydrogen sulfide, rust, and other contaminants. [Pg.217]

Potassium amyl xanthate Potassium ethyl xanthate Sodium isobutyl xanthate Sodium isopropyl xanthate flotation collector, gold ore Sodium di-s-butyl dithiophosphate flotation collector, iron sulfide Ammonium dibutyl dithiophosphate flotation collector, lead Ammonium dibutyl dithiophosphate Sodium diethyidithiocarbamate... [Pg.5295]

Dinitrotoluene is oxidized to 2,4-dinitrobenzoic acid [610-30-0] by potassium permanganate or chromic acid, and is reduced to 2,4-diaminotoluene by iron and acetic acid. It is reduced partially by zinc chloride and hydrochloric acid to 2-amino-4-nitrotoluene [99-55-8] and by ammonium sulfide to 4-amino-2-nitrotoluene [119-32-4],... [Pg.71]

The iodate is a poison potassium iodide, however, is used in foodstuffs. Thus the iodate must be completely removed frequently by a final reduction with carbon. After re-solution in water, further purification is carried out before recrystallization. Iron, barium, carbonate, and hydrogen sulfide are used to effect precipitation of sulfates and heavy metals. [Pg.534]

At room temperature, sulfur unites readily with copper, silver, and mercury and vigorously with sodium, potassium, calcium, strontium, and barium to form sulfides. Iron, chromium, tungsten, nickel, and cobalt react much less readily. In a finely divided state, zinc, tin, iron, and aluminum react with sulfur on heating (19). [Pg.117]

The modem process uses a potassium-sulfate-promoted vanadium(V) oxide catalyst on a silica or kie,selguhr support. The SO2 is obtained either by burning pure sulfur or by roasting sulfide minerals (p. 651) notably iron pyrite, or ores of Cu, Ni and Zn during the production of these metals. On a worldwide basis about 65% of the SO2 comes from the burning of sulfur and some 35% by the roasting of sulfide ores but in some countries (e.g, the UK) over 95% conies from the former. [Pg.708]


See other pages where Potassium iron sulfide is mentioned: [Pg.585]    [Pg.481]    [Pg.389]    [Pg.88]    [Pg.182]    [Pg.893]    [Pg.220]    [Pg.478]    [Pg.1258]    [Pg.132]    [Pg.269]    [Pg.561]    [Pg.585]    [Pg.341]    [Pg.418]    [Pg.975]    [Pg.230]    [Pg.1031]    [Pg.233]    [Pg.689]    [Pg.41]    [Pg.824]    [Pg.700]    [Pg.535]    [Pg.1540]    [Pg.442]    [Pg.326]    [Pg.332]   
See also in sourсe #XX -- [ Pg.1507 ]




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