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Fluoride carbonates

The chlorides, bromides, nitrates, bromates, and perchlorate salts ate soluble in water and, when the aqueous solutions evaporate, precipitate as hydrated crystalline salts. The acetates, iodates, and iodides ate somewhat less soluble. The sulfates ate sparingly soluble and ate unique in that they have a negative solubitity trend with increasing temperature. The oxides, sulfides, fluorides, carbonates, oxalates, and phosphates ate insoluble in water. The oxalate, which is important in the recovery of lanthanides from solutions, can be calcined directly to the oxide. This procedure is used both in analytical and industrial apptications. [Pg.541]

CARBON OXYFLUORIDE see CARBONYL FLUORIDE CARBON REMOVER, LIQUID CARBON TETRABROMIDE CARBON TETRACHLORIDE... [Pg.207]

CYANOGEN BROMIDE CYANOGEN CHLORIDE CYANOGEN FLUORIDE CARBON MONOXIDE CARBONYL SULFIDE CARBON OXYSELENIDE CARBON DIOXIDE CARBON DISULFIDE CARBON SELENOSULFIDE CYANOGEN... [Pg.203]

I. Cabasso, Y. Yuan, and X. Xu. Gas diffusion electrodes based on poly(vinylidene fluoride) carbon blends. US Patent 5783325 (1998). [Pg.295]

In aqueous media lutetium occurs as tripositive Lu3+ ion. All its compounds are in +3 valence state. Aqueous solutions of all its salts are colorless, while in dry form they are white crystalline solids. The soluble salts such as chloride, bromide, iodide, nitrate, sulfate and acetate form hydrates upon crystallization. The oxide, hydroxide, fluoride, carbonate, phosphate, and oxalate of the metal are insoluble in water. The metal dissolves in acids forming the corresponding salts upon evaporation of the solution and crystallization. [Pg.510]

Tojo, T. Fluorine - Carbon and Fluoride - Carbon Materials Marcel Dekker New York. 1995 Chapter 9. [Pg.166]

Organogermanes R, GeX (X = H, MeO, Cl, Br) do not react with antimony(V) fluoride/carbon, but allyl —germanium bond breaking occurs under mild conditions (24 h at 25 C in diethyl ether), and in high yields (80-85%), leading to the corresponding fluorogermanes.101... [Pg.522]

Nakajima, T. Fluorine-C.arhon and Fluoride-Carbon Materials Chemistry, Physics, and Applications Dekker New York, 1995. [Pg.483]

Nakajima T (ed) (1994) Fluorine-carbon and fluoride-carbon materials. Chemistry physics and applications. Marcel Dekker, New York Pirronello V, Avema D (1998) Astronom Astrophys 196 201 Pirronello V, Liu C, Shen L, Vidali G (1997a) Astrophys J Lett 475 L69 Pirronello V, Biham O, Liu C, Shen L, Vidali G (1997b) Astrophys J Lett 483 L131 Pirronello V, Liu C, Roser JE, Vidali G (1999) Astronom Astrophys 344 681 Somoraj GA (1994) Introduction to surface chemistry and catalysis. Wiley-Interscience, New York Smoluchowski R (1983) J Phys Chem 21 4229... [Pg.53]

Adcock, W. and Abeywickrema, A.N., Concerning the origin of substituent-induced fluorine-19 chemical shifts in aliphatic fluorides carbon-13 and fluorine-19 nuclear magnetic resonance study of l-fluoro-4-phenylbicyclo[2,2,2]octanes substituted in the arene ring, J. Org. Chem., 47, 2945, 1982. [Pg.443]

The fluorine produced is either immediately used to prepare other final products or is first liquefied and delivered in steel cylinders where required. When fluorine is liquefied it is first led from the electrolyzer through a steel coil cooled to — 90 °C by dry ice. It then passes through a coil submerged in liquid oxygen, (— 183 °C) to separate the remaining traces of hydrogen fluoride, carbon dioxide and tetrafluoromethane. The product still contains a small... [Pg.383]

R. Yazami, In Fluorine-Carbon, Fluoride-Carbon Materials, by T. Nakajima (Ed.), Marcel Dekker, Inc., New York, NY, 1995, Chapter 7. [Pg.520]

The chloride, bromide, bromate, perchlorate, nitrate, acetate, and iodide salts are all soluble in water, the sulfates sparingly soluble, and the fluorides, carbonates, oxalates, and phosphates insoluble. [Pg.38]

Complex Ion Formation. Formation of complexes of lead with the various anions such as chloride, fluoride, carbonate, bicarbonate, and hydroxide increases the concentration of lead in natural waters by preventing lead from taking part in other chemical reactions, primarily adsorption, that would lower its... [Pg.237]

M. Kawaguchi and N. Bartlett, Syntheses, Structures, and Intercalation Chemistry of B/C/N Materials Based on the Graphite Network, Fluorine-Carbon and Fluoride Carbon Materials, ed. T. Nakajima, Marcel Dekker Inc., New York (1995) 187-238. [Pg.603]

Apart from the fluorides, halogen compounds are very sensitive to radiolysis and evidence suggests that the predominant primary process is one of rupture at the carbon-halogen With fluorides, carbon-carbon bond... [Pg.203]

Ammonium uranyl carbonate (AUC) process This process was developed in the 1960 s in the Federal Republic of Germany. It comprises the simultaneous feeding of uranium(Vl) fluoride, carbon dioxide and ammonia into an aqueous ammonium carbonate solution at 70°C, whereupon tetra-ammonium tricarbonato-dioxo-uranate (ammonium uranyl carbonate) precipitates out ... [Pg.612]


See other pages where Fluoride carbonates is mentioned: [Pg.365]    [Pg.114]    [Pg.41]    [Pg.294]    [Pg.10]    [Pg.294]    [Pg.11]    [Pg.13]    [Pg.136]    [Pg.138]    [Pg.522]    [Pg.531]    [Pg.301]    [Pg.88]    [Pg.17]    [Pg.17]    [Pg.62]    [Pg.1332]    [Pg.62]    [Pg.172]    [Pg.11]    [Pg.13]    [Pg.236]    [Pg.294]    [Pg.110]    [Pg.114]    [Pg.62]   
See also in sourсe #XX -- [ Pg.17 ]




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Asymmetric carbon-fluoride bond

Asymmetric carbon-fluoride bond formation

Calcium carbonates fluoride

Carbon fluoride oxide

Carbon fluorides

Carbon fluorides

Carbon monoxide complex with hydrogen fluoride

Carbon tetrachloride reaction with hydrogen fluoride

Carbon-fluoride bond formation

Carbon-fluoride bond, stability

Carbon-sulfur bonds tetrabutylammonium fluoride

Carbonic ester fluorides

Fluorides carbon halides

Fluorides carbon—sulfur bonds

Fluorides of Beryllium, Boron, and Carbon

Lithium-Carbon Fluoride Battery

Methyl fluoride carbon

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