Potassium iron fluoride

Potassium iron fluoride, 441 Potassium manganese fluoride, 441 Potassium molybate, 440-444, 450, 466f, 471 Potassium nickel fluoride, 454f Potassium sulphide, selenide, telluride. See Fluorites... 

Hirakawa, K., and T. HasMmoto Magnetic properties of potassium iron group fluorides KMFj. J. Phys. Soc. Japan 15, 2063 (1960). 

In 1808 Sir Humphry Davy tried in vain to decompose zirconia with the electric current, but Berzelius (36) finally obtained the metal in 1824 by heating a dry mixture of potassium and potassium zirconium fluoride in a very small closed iron tube placed inside a platinum crucible. After the quiet reaction had taken place, he cooled the tube and placed it in distilled water, whereupon, to use his own words, There fell from the tube a black powder as fast as the salt dissolved, and at the same time there was evolved a small quantity of hydrogen.. . . The zirconium obtained in this manner is easily deposited. It can be washed with water without oxidizing. Washed and dried, it forms a black powder resembling charcoal, which cannot be compressed nor polished like a metal (15). 

Aluminium alloys well with up to about 3-5 per cent, of tantalum, which has no effect, however, on the mechanical strength, ductility, and working properties of aluminium.3 Reduction of tantalum pentoxide by the thermite process yields hard, brittle alloys.1 A substance the composition of which corresponds with the formula TaAls has been obtained by reducing potassium tantalum fluoride, K2TaF7, with aluminium filings at a high temperature. It is described as an iron-grey crystalline powder, of density 7-02, which is scarcely attacked by acids.5... 

The potassium promoter is usually added as the carbonate but it was shown that the hydroxide, nitrate, fluoride, and the like, gave simQar results [15]. Highly-dispersed catalysts are formed when potassium/iron complex salts such as K Fe(C0)4 are supported on AljOj orSiOj [58]. After reduction,... 

Platinum is attacked only slowly by fluorine. Copper and steel can be used as containers lor the gas they are attacked by it, but become coated with a thin layer of copper fluoride or iron fluoride which then protects them against further attack. Fluorine was first made in 1886 by the French chemist Henri Moissan (1852-1907), by the electrolysis of a solution of potassium fluoride, KF, m liquid hydrogen fluoride, HF. In recent years methods for its commercial production and transport (in steel tanks) have been developed, and it is now used in chemical industry in moderate quantities. 

M S04 Mn2(S04>3 24H2O manganese(II) carbonate hydroxyphenylacetic acid manganese hydroxide monoammonium phosphate potassium tm(II) sulphate ammonium sulphate yellow lead monoxide ammonium hydrogen fluoride potassium iron(III) sulphate mercury(n) isocyanate hexamethylbenzene tetramethyldiamino-benzophenone... 

Several breakdown processes have been used in which the ore is reacted with a fused or sintered fluorinating agent such as potassium hydrogen fluoride or sodium silicofluoride. The most important of these is the Copaux-Kawecki process for opening beryl ore. This is in many ways a unique process and other processes are unlikely to have many features in common with it apart from the problems associated with the handling of toxic fluorides. Since the fluorine is in combination with sodium, as the simple fluoride or as stable complexes with silicon and iron, the severe corrosion conditions inherent in many other fluorination reactions are almost absent in this case. 

Procedure. A drop of the add test solution is placed in a porcelain micro crucible coated with paraffine. The yellow solution is decolorized by adding a few crystals of potassium fluoride. Then a drop of the reagent solution is added. In the presence of iron salts, a red or pink coloration appears. In the absence of ferrous salts, the solution remains colorless, or a precipitate (complex potassium ferric fluoride) may separate. 

A number of mineral substances are gaseous at the magmatic temperatures of volcanoes and are mobilized with volcanic gases. These kinds of substances condense near the mouths of volcanic fiimaroles and are called sublimates. Elemental sulfur is a common sublimate. Some oxides, particularly of iron and silicon, are deposited as sublimates. Most other sublimates consist of chloride and sulfate salts. The cations most commonly involved are monovalent cations of ammonium ion, sodium, and potassium magnesium calcium aluminum and iron. Fluoride and chloride sublimates are sources of gaseous HF and HCl formed by their reactions at high temperatures with water, such as the following ... 

Once purification of the niobium has been effected, the niobium can be reduced to the metallic form. The double fluoride salt with potassium, K2NbFy, can be reduced using sodium metal. The reaction is carried out in a cylindrical iron vessel filled with alternating layers of K NbF and oxygen-free sodium ... 

Use of excess sodium drives the reaction, usually done under an argon or helium blanket, to completion. After cooling, the excess sodium is leached with alcohol and the sodium and potassium fluorides are extracted with water, leaving a mass of metal powder. The metal powder is leached with hydrochloric acid to remove iron contamination from the cmcible. 

Tetrapotassium peroxodiphosphate is produced by electrolysis of a solution containing dipotassium phosphate and potassium fluoride (52). Alkalinity favors the formation of the P20 g anion, whereas the PO anion is produced in larger yields in acidic solution. It is therefore possible to obtain an 80% yield of K4P20g by choosing the proper conditions. The tetrapotassium peroxodiphosphate can be crysta11i2ed from solution by evaporation of water to form a slurry. The crystals can be separated from the slurry and dried. The material is noncorrosive and cannot be catalyticaHy decomposed by iron ions. 

The conversion of octachloronaphthalene to octafluoronaphthalene with potassium fluoride and either 18-crown-6, dibenzo-18-crown-6, cis,j>m,cis-dicyclohexano-18-crown-6, cis,anti,cis-dicyclohexano-l 8-crown-6, or irons,syn,trails-dicyclohexano-18-crown-6 demonstrates that 18-crown-6 or dibenzo-18-crown-5 increases the yield and selecuvity and decreases the reaction time [55] Treatment of 3,4-dichloro-],2,5-thiadiazole with potassium fluonde in sulfolane with and without 18-crown-6 present shows that less severe conditions can be used with either 18-crown-6 or dibenzo-18-crown-6 to form 3,4-difluoro-l,2,5-thiadiazole (equation 34)... 

Brom-benzol, n. bromobenzene. calcium, n. calcium bromide, -cyan, n. cyanogen bromide, bromocyanogen. -dampf, tn. bromine vapor, -eisen, n. iron bromide, -fiasche, /. bromine bottle, -fluor, n. bromine fluoride, -gehalt, tn. bromine content, -gold, n. gold bromide, -goldkalium, n. potassium auri-bromide, potassium bromoaurate. bromhaltig, a. contaim ng bromine, Brom-hydrat, n. hydrobromide bromine hydrate. -hydrin, n. bromohydrin. 

Dissolved mineral salts The principal ions found in water are calcium, magnesium, sodium, bicarbonate, sulphate, chloride and nitrate. A few parts per million of iron or manganese may sometimes be present and there may be traces of potassium salts, whose behaviour is very similar to that of sodium salts. From the corrosion point of view the small quantities of other acid radicals present, e.g. nitrite, phosphate, iodide, bromide and fluoride, have little significance. Larger concentrations of some of these ions, notably nitrite and phosphate, may act as corrosion inhibitors, but the small quantities present in natural waters will have little effect. Some of the minor constituents have other beneficial or harmful effects, e.g. there is an optimum concentration of fluoride for control of dental caries and very low iodide or high nitrate concentrations are objectionable on medical grounds. 

Mesitaldehyde may be prepared from mesitylmagnesium bromide by the reaction with orthoformate esters3 or ethoxy-methyleneaniline 3 from acetylmesitylene by oxidation with potassium permanganate,4 from mesitoyl chloride by reduction,5 from mesityllithium by the reaction with iron pentacarbonyl and from mesitylene by treatment with formyl fluoride and boron trifluoride,7 by treatment with carbon monoxide, hydrogen chloride, and aluminum chloride,8 or by various applications of the Gatterman synthesis.9-11... 

It is therefore possible to determine cations such as Ca2+, Mg2+, Pb2+, and Mn2+ in the presence of the above-mentioned metals by masking with an excess of potassium or sodium cyanide. A small amount of iron may be masked by cyanide if it is first reduced to the iron(II) state by the addition of ascorbic acid. Titanium(IV), iron(III), and aluminium can be masked with triethanolamine mercury with iodide ions and aluminium, iron(III), titanium(lV), and tin(II) with ammonium fluoride (the cations of the alkaline-earth metals yield slightly soluble fluorides). 

Discussion. This method is based upon the precipitation of lead chlorofluoride, in which the chlorine is determined by Volhard s method, and from this result the fluorine content can be calculated. The advantages of the method are, the precipitate is granular, settles readily, and is easily filtered the factor for conversion to fluorine is low the procedure is carried out at pH 3.6-5.6, so that substances which might be co-predpitated, such as phosphates, sulphates, chromates, and carbonates, do not interfere. Aluminium must be entirely absent, since even very small quantities cause low results a similar effect is produced by boron ( >0.05 g), ammonium (>0.5 g), and sodium or potassium ( > 10g) in the presence of about 0.1 g of fluoride. Iron must be removed, but zinc is without effect. Silica does not vitiate the method, but causes difficulties in filtration. 

This reaction takes place quite rapidly on boiling, and hence hydrochloric add cannot be used in oxidations which necessitate boiling with excess of cerium(lV) sulphate in add solution sulphuric add must be used in such oxidations. However, direct titration with cerium(IV) sulphate in a dilute hydrochloric add medium, e.g. for iron(II) may be accurately performed at room temperature, and in this respect cerium(IV) sulphate is superior to potassium permanganate [cf. (2) above]. The presence of hydrofluoric add is harmful, since fluoride ion forms a stable complex with Ce(lV) and decolorises the yellow solution. 

The cobalt complex is usually formed in a hot acetate-acetic acid medium. After the formation of the cobalt colour, hydrochloric acid or nitric acid is added to decompose the complexes of most of the other heavy metals present. Iron, copper, cerium(IV), chromium(III and VI), nickel, vanadyl vanadium, and copper interfere when present in appreciable quantities. Excess of the reagent minimises the interference of iron(II) iron(III) can be removed by diethyl ether extraction from a hydrochloric acid solution. Most of the interferences can be eliminated by treatment with potassium bromate, followed by the addition of an alkali fluoride. Cobalt may also be isolated by dithizone extraction from a basic medium after copper has been removed (if necessary) from acidic solution. An alumina column may also be used to adsorb the cobalt nitroso-R-chelate anion in the presence of perchloric acid, the other elements are eluted with warm 1M nitric acid, and finally the cobalt complex with 1M sulphuric acid, and the absorbance measured at 500 nm. 

Antimony, arsenic, selenium, tellurium, iridium, iron, molybdenum, osmium, potassium, rhodium, tungsten (and when primed with charcoal,) aluminium, copper, lead, magnesium, silver, tin, zinc. Interaction of lithium or calcium with chlorine tri- or penta-fluorides is hypergolic and particularly energetic. 

When nitryl fluoride is passed at ambient temperature over molybdenum, potassium, sodium, thorium, uranium or zirconium, glowing or white incandescence occurs. Mild warming is needed to initiate similar reactions of aluminium, cadmium, cobalt, iron, nickel, titanium, tungsten, vanadium or zinc, and 200-300°C for lithium or manganese. 

Ferric chloride hexahydrate Iron chloride, hexahydrate (8,9) (10025-77-1) Potassium fluoride (8,9) (7789-23-3)... 

Quinoline Salicylic acid Silicon Dinitrogen tetroxide, linseed oil, maleic anhydride, thionyl chloride Iodine, iron salts, lead acetate Alkali carbonates, calcium, chlorine, cobalt(II) fluoride, manganese trifluoride, oxidants, silver fluoride, sodium-potassium alloy... 

In all 28 parameters were individually mapped alkalinity, aluminum, antimony, arsenic, barium, boron, bromide, cadmium, calcium, chloride, chromium, conductivity, copper, fluoride, hardness, iron, lead, magnesium, manganese, nitrate, pH, potassium, selenium, sodium, sulphate, thallium, uranium, and zinc. These parameters constitute the standard inorganic analysis conducted at the DENV Analytical Services Laboratory. 

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