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Metal acetylides calcium acetylide

Metal acetylides or carbides Calcium carbide 3.97/46 See Caesium acetylide Mineral acids Rubidium acetylide Acids Uranium dicarbide Hydrogen chloride... [Pg.1349]

Metal acetylides incandesce on heating in selenium vapour barium acetylide at 150°C, calcium acetylide and strontium acetylide at 500°C and thorium carbide at an unstated temperature. [Pg.1906]

Catalytic forms of copper, mercury and silver acetylides, supported on alumina, carbon or silica and used for polymerisation of alkanes, are relatively stable [3], In contact with acetylene, silver and mercury salts will also give explosive acetylides, the mercury derivatives being complex [4], Many of the metal acetylides react violently with oxidants. Impact sensitivities of the dry copper derivatives of acetylene, buten-3-yne and l,3-hexadien-5-yne were determined as 2.4, 2.4 and 4.0 kg m, respectively. The copper derivative of a polyacetylene mixture generated by low-temperature polymerisation of acetylene detonated under 1.2 kg m impact. Sensitivities were much lower for the moist compounds [5], Explosive copper and silver derivatives give non-explosive complexes with trimethyl-, tributyl- or triphenyl-phosphine [6], Formation of silver acetylide on silver-containing solders needs higher acetylene and ammonia concentrations than for formation of copper acetylide. Acetylides are always formed on brass and copper or on silver-containing solders in an atmosphere of acetylene derived from calcium carbide (and which contains traces of phosphine). Silver acetylide is a more efficient explosion initiator than copper acetylide [7],... [Pg.222]

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]

Several of the mono- and di-alkali metal acetylides and copper acetylides ignite at ambient temperature or on slight warming, with either liquid or vapour. The alkaline earth, iron, uranium and zirconium carbides ignite in the vapour on heating. See Calcium acetylide Halogens... [Pg.106]

FERRIC OXIDE (1309-37-1) FcjO, Violent reactions with powdered aluminum (thermite reaction), hydrogen peroxide, calcium disilicide (thermite reaction), ethylene oxide (may cause explosive polymerization), calcium hypochlorite, hydrazine, hydrogen trisulfide, powdered magnesium. Contact with carbon monoxide may cause fire or explosion. Incompatible with calcium carbide (powdered), chlorides, guanidinium perchlorate, metal acetylides. Contact with the explosive hydrazinium diperchlorate or ammonium perchlorate can increase heat-, mechanical shock-, or friction sensitivity. Incompatible with aluminum-magnesium-zinc alloys. Spent material... [Pg.496]

LEAD PROTOXIDE (1317-36-8) PbO An oxidizer. Explosive reaction with 90% peroxyformic acid, mbidium acetylide. Reacts violently with strong oxidizers, aluminum carbide boron, chlorine, fluorine, dichloromethylsilane, calcium sulfide, hydrogen peroxide, hydrogen trisulfide (ignition), hydroxylamine (ignition), lithium carbide, metal acetylides, metal powders (e.g., aluminum, molybdenum, sodium, zirconium, etc.), perchloric acid, red phosphoms, selenium oxychloride, sodium. [Pg.631]

ACIDE CHLORHYDRIQUE (French) (7647-01-0) Hydrogen chloride gas is quickly absorbed in water, forming hydrochloric acid. Hydrochloric acid is a strong acid. Violent reaction with bases, strong oxidizers (with release of chlorine gas), acetic anhydride, cesium cyanotridecahydrodecaborate(2-), ethylidine difluoride, hexalithium disilicide, metal acetylides. sodium, silicon dioxide, tetraselenium tetranitride, and many organic materials. Incompatible with aliphatic amines, alkanolamines, alkylene oxides, aluminum, aluminum-titanium alloys, aromatic amines, amides, 2-aminoethanol, ammonia, ammonium hydroxide, calcium phosphide, chlorosulfonic acid, ethylene diamine, ethyleneimine, epichlorohydrin, isocyanates, metal acetylides, metal carbides, oleum, organic anhydrides, perchloric acid,... [Pg.24]


See other pages where Metal acetylides calcium acetylide is mentioned: [Pg.113]    [Pg.1647]    [Pg.1715]    [Pg.1908]    [Pg.1393]    [Pg.1716]    [Pg.1996]    [Pg.106]    [Pg.1647]    [Pg.1715]    [Pg.1908]    [Pg.670]    [Pg.772]    [Pg.827]    [Pg.130]    [Pg.85]    [Pg.154]    [Pg.245]    [Pg.245]    [Pg.555]    [Pg.557]    [Pg.559]    [Pg.560]    [Pg.629]    [Pg.630]    [Pg.630]    [Pg.631]    [Pg.631]    [Pg.748]    [Pg.751]    [Pg.768]    [Pg.783]    [Pg.28]    [Pg.28]    [Pg.114]   
See also in sourсe #XX -- [ Pg.594 ]




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Acetylide

Acetylides

Acetylides calcium acetylide

Calcium metal

Calcium, Metallic

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