Sulfides antimony sulfide

Mixtures with gold(III) sulfide, antimony sulfide or mercury(II) sulfide ignite on grinding. 

The heat sensitivity (above) may explain the explosions which occur on contact of many readily oxidisable materials with this powerful oxidant. Such materials include ammonia, potassium arsenic, antimony sulfur, charcoal (adsorptive heating may also contribute) calcium phosphide, phosphine, phosphorus hydrogen sulfide, antimony sulfide, barium sulfide, mercury sulfide and tin sulfide [1], Various organic materials (paper, cork, rubber, turpentine, etc.) behave similarly [2]. Mixtures with hydrogen detonate on ignition [1]. 

Antimony sulfide Antimony (V) sulfide Antimony sulfide golden Cl 77061 Golden antimony sulfide... 

Other early match-like devices were based on the property of various combustible substances mixed with potassium chlorate to ignite when moistened with strong acid. More important was the property of chlorates to form mixtures with combustibles of low ignition point which were ignited by friction (John Walker, 1827). However, such matches containing essentially potassium chlorate, antimony sulfide, and later sulfur (lucifers), mbbed within a fold of glass powder-coated paper, were hard to initiate and unreHable. 

Iron Precipitation. Rich sulfide ore or Hquated antimony sulfide (cmde antimony) is reduced to metal by iron precipitation. This process, consisting essentially of heating molten antimony sulfide ia cmcibles with slightly more than the theoretical amount of fine iron scrap, depends on the abihty of iron to displace antimony from molten antimony sulfide. Sodium sulfate and carbon are added to produce sodium sulfide, or salt is added to form a light fusible matte with iron sulfide and to faciHtate separation of the metal. Because the metal so formed contains considerable iron and some sulfur, a second fusion with some Hquated antimony sulfide and salt foHows for purification. 

Microbiological leaching of copper and uranium has been commercially developed and research has iadicated that microorganisms may be used to oxidize complex antimony sulfide minerals (22,23). If this technology is developed commercially, it may aHow for the exploitation of many low grade antimony deposits. 

Antimony Trisulfide. Antimony(III) sulfide (antimony sesquisulftde) [1345-04-6] SbS, exists as a black crystalline soHd, stibnite [1317-86-8] and as an amorphous red to yeUow-orange powder. Stibnite melts at 550°C and has Ai i° 298 175 kJ/mol (—41.8 kcal/mol)) A°29g, 182 J/(182 mol-K) [43.5 cal/(43.5 mol-K)] for the amorphous soHd AH° 298 1 147 kJ/mol (—35.1 kcal/mol) (38). The crystal stmcture of stibnite contains two distiucdy different antimony sites and consists of two parallel Sb S chains that are linked together to form cmmpled sheets (two per unit cell). 

Formulations of this type have completely replaced earlier "strike anywhere matches based on (poi.sonous) white P4, sulfur, and KCIO3. though safety matches" still use a match head which is predominantly KCIO3 struck against the side of the match-box which has been covered with a paste of (non-toxic) red P (49.5%), antimony sulfide (27.6%). FeiOr (l.2%) and gum arabic (2I,7%). About lO" matches are used annually in the UK alone. 

Antimon-saure, /. antimonic acid, -saureanhy-drid, n. antimonic anhydride, antimony pent-oxide. -silber, n. antimonial silver, dyscrasite. -silberblende,/. pyrargyrite. -silberglanz, m. stephanite. -spiegel, m. antimony mirror, -sulfid, n. antimony sulfide, specif, antimony pentasulfide, antimony(V) sulfide, -sulfiir, n. antimony trisulfide, antimony(III) sulfide, -yerblndung,/. antimony compound, -wasser--stoff, m. antimony hydride, stibine. -weiss, n. antimony white (Sb Oa). -zinnober, m. kermes mineral. 

Schwefel-. of sulfur, sulfur, sulfuric, sulfide of, thio-. siilfo-. -abdruck, m. sulfiir print, -alkali, n. alkali siilfide. -alkohol, m. siilfur alcohol, thiol carbon disulfide (old name), -ammonium, -ammon, n. ammonium sulfide, -antlmon, n. antimony sulfide, -antimonblei, n, antimony lead sulfide (Min.) boulanger-ite. 

SpiessglanZ kermes, m. kermesite kermes mineral, -kbnig, m. regulus of antimony, -leber,/. livex of antimony, hepar antimonii. -metall, n. antimony, -mittel, n. antimonial remedy, -mohr, m. aethiops antimonialis (old pharmaceutical preparation of mercury and antimony sulfides). -ocker, m, antimony ocher, -oxyd,n. antimon> trioxide. -safran,... 

Perkins Explosive. A primary mixt patented in Engl in 1870 contg amorph P, metallic sulfides (such as antimony sulfide), and K chlorate or nitrate... 

Chlorates are useful oxidizing agents. Potassium chlorate is used as an oxidant in fireworks and in matches. The heads of safety matches consist of a paste of potassium chlorate, antimony sulfide, and sulfur, with powdered glass to create friction when the match is struck as mentioned in Section 15.1, the striking strip contains red phosphorus, which ignites the match head. 

Red phosphorus is found in the striking surface of matchboxes. The red heads contain antimony sulfide. 

Semimetal that occurs as a tin-type, brittle form and as a yellow, unstable, nonmetallic form. Its main use is in alloys to harden other metals. Without the addition of antimony, lead would have remained the "softy" of the Periodic Table. But with antimony, lead ruled the print world and later found use in the production of rechargeable batteries. It can be found in older ceramic glazing (yellow orange). Everyday encounters antimony sulfide in match heads and red rubber, antimony oxide is used as a flame retardant. Pure antimony is starting to become of interest in the electronics sector. 

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