Potassium oxides, names

Potassium perchlorate (KP KCIO4) is a weU-known oxidizer, used as an oxidizer component of black powder. Since KP produces potassium oxides and condensed products, the high molecular mass Mg of the combustion products is not favorable for its use as an oxidizer in rocket propellants. A mixture of 75 % KP with 25 % asphalt pitch was used as a rocket propellant named Galcit, which was the original prototype of a composite propellant in the 1940 s. Potassium chlorate (KCIO3) is also a crystalline oxidizer, and although it has a lower oxygen content compared... 

Metallic oxidants, namely, chromic acid and potassium permanganate, may be used to oxidize alkanes to alcohols or ketones, but these reagents have only limited synthetic value. Alkaline KMnC>4 is rather ineffective, mainly because of the insolubility of alkanes in the aqueous solution of the reagent. Oxidations in acidic solutions such as aqueous CF3COOH,108 or the use of special reagents such as benzyltriethylammonium permanganate109 may give better results. 

This Table names a large number of homoatomic and binary compounds and species, and some heteropolynuclear entities, and thus may be used as a reference for names of simple compounds and a source of examples to guide in the naming of further compounds. It may be necessary to browse the Table to find (families of) compounds that match those of interest. For example, all the oxides of potassium are named corresponding compounds of the other alkali metals, not included here, are named analogously. Several silicon and germanium hydride species are named names for corresponding tin and lead species are not necessarily included. 

Compounds consisting of two elements, or of an element and a radical only, binary compounds, are designated by compound names made up of the name of the more electro-positive, followed by that of the more electro-negative, in which the termination ide has been substituted for tbe terminations ine. on, ogen, ygm, orus, turn, and ur. For example the compound of potassium and chlorine is called potassium chloride, that of potassium and oxygen, potassium oxide, that of potassium and phosphorus, potassium phosphide. 

In the trade, potassium-containing compounds or salts that are applied primarily as a source of this nutrient or that find use in industry are referred to as potash. The name derives from an early production method in which potassium carbonate, leached from wood ashes, was crystallized by evaporating the leachate in large iron pots. The salt potassium chloride (muriate, muriate of potash, or KCl) is now the major source of the element (95%) other important salts are potassium sulfate (potassium sulphate, K2SO4, or sulphate of potash), potassium magnesium sulfates of varying K/Mg ratios, and potassium nitrate (KNO3). The fertilizer industry expresses the potassium content of fertilizer salts in terms of the potassium oxide (K2O) content, not as the K content. Muriate thus contains 60 percent + of K2O—which equates with 49.8 percent-h of potassium (K). 

By the interaction of aleohols or glyeols with potassium iodide and 95 per eent. orthophosphoric aeid (the last named is prepared from the eommercial 85 per eent. aeid and phosphoric oxide), for example ... 

Ninhydrin (also named 1 2 3-triketoindane or 1 2 3-triketohydrindene hydrate) is prepared most simply from the inexpensive phthahc anhydride (I). The latter is condensed with acetic anhydride In the presence of potassium acetate to give phthalylacetlc acid (II) reaction of the latter with sodium methoxide in methanol yields 1 3-indanedionecarboxyhc acid, which is decomposed upon warming with dilute hydrochloric or sulphuric acid to indane-1 3-dione (or 1 3-diketohydrindene) (HI). Selenium dioxide oxidation of (III) afibrds indane-1 2 3-trione hydrate (ninhydrin) (IV). 

Seaweeds. The eadiest successful manufacture of iodine started in 1817 using certain varieties of seaweeds. The seaweed was dried, burned, and the ash lixiviated to obtain iodine and potassium and sodium salts. The first process used was known as the kelp, or native, process. The name kelp, initially apphed to the ash of the seaweed, has been extended to include the seaweed itself. About 20 t of fresh seaweed was used to produce 5 t of air-dried product containing a mean of 0.38 wt % iodine in the form of iodides of alkah metals. The ash obtained after burning the dried seaweed contains about 1.5 wt % iodine. Chemical separation of the iodine was performed by lixiviation of the burned kelp, followed by soHd-Hquid separation and water evaporation. After separating sodium and potassium chloride, and sodium carbonate, the mother Hquor containing iodine as iodide was treated with sulfuric acid and manganese dioxide to oxidize the iodide to free iodine, which was sublimed and condensed in earthenware pipes (57). 

Prussian Blue. Reaction of [Fe(CN)3] with an excess of aqueous h on(Ill) produces the finely divided, intensely blue precipitate Pmssian Blue [1403843-8] (tetrairon(Ill) tris(hexakiscyanoferrate)), Fe4[Fe(CN)3]. Pmssian Blue is identical to Turnbull s Blue, the name which originally was given to the material produced by reaction of [Fe(CN)3] with excess aqueous h on(Il). The soHd contains or has absorbed on its surface a large and variable number of water molecules, potassium ions (if present in the reaction), and h on(Ill) oxide. The h on(Il) centers are low spin and diamagnetic h on(Ill) centers are high spin. Variations of composition and properties result from variations in reaction conditions. Rapid precipitation in the presence of potassium ion affords a colloidal suspension of Pmssian Blue [25869-98-1] which has the approximate composition KFe[Fe(CN)3]. Pmssian Blue compounds are used as pigments in inks and paints and its formation on sensitized paper is utilized in the production of blueprints. 

Dry basis natural mbber compound recipe, in part by wt high ammonia natural latex mbber concentrate, 100.0 potassium hydroxide, 0.5 Nacconal 90F (alkylarenesulfonate (AHied Chemical Co.)), 1.0 zinc oxide, 3.0 sulfur, 1.0 ZMBT, 1.0 zinc diethyldithiocarbamate (ZEDC) (trade names Ethazate (Uniroyal, Inc.), Ethyl Zimate (R. T. Vanderbilt), 0.3 antioxidant, as indicated. Wet-basis natural mbber compound recipe, in parts by wt natural latex (NC 356), 167.9 potassium hydroxide, 2.5 Nacconal 90F, 5.0 zinc oxide, 5.45 sulfur, 1.65 ZMBT, 2.0 ZEDC, 2.0 antioxidant, as indicated. AH films poured from freshly mixed compounds, dried overnight in place, then lifted and dried 1 h in air at 50°C before curing. 

Polyether Polyols. Polyether polyols are addition products derived from cyclic ethers (Table 4). The alkylene oxide polymerisation is usually initiated by alkah hydroxides, especially potassium hydroxide. In the base-catalysed polymerisation of propylene oxide, some rearrangement occurs to give aHyl alcohol. Further reaction of aHyl alcohol with propylene oxide produces a monofunctional alcohol. Therefore, polyether polyols derived from propylene oxide are not truly diftmctional. By using sine hexacyano cobaltate as catalyst, a more diftmctional polyol is obtained (20). Olin has introduced the diftmctional polyether polyols under the trade name POLY-L. Trichlorobutylene oxide-derived polyether polyols are useful as reactive fire retardants. Poly(tetramethylene glycol) (PTMG) is produced in the acid-catalysed homopolymerisation of tetrahydrofuran. Copolymers derived from tetrahydrofuran and ethylene oxide are also produced. 

The primary Cr—O bonded species is cbromium (VT) oxide, CrO, which is better known as chromic acid [1115-74-5], the commercial and common name. This compound also has the aliases chromic trioxide and chromic acid anhydride and shows some similarity to SO. The crystals consist of infinite chains of vertex-shared CrO tetrahedra and are obtained as an orange-red precipitate from the addition of sulfuric acid to the potassium or sodium dichromate(VI). Completely dry CrO is very dark red to red purple, but the compound is deflquescent and even traces of water give the normal mby red color. Cbromium (VT) oxide is a very powerful oxidi2er and contact with oxidi2able organic compounds may cause fires or explosions. 

The chemistry of ethyl alcohol is largely that of the hydroxyl group, namely, reactions of dehydration, dehydrogenation, oxidation, and esterification. The hydrogen atom of the hydroxyl group can be replaced by an active metal, such as sodium, potassium, and calcium, to form a metal ethoxide (ethylate) with the evolution of hydrogen gas (see Alkoxides, metal). 

Resoles are usually those phenolics made under alkaline conditions with an excess of aldehyde. The name denotes a phenol alcohol, which is the dominant species in most resoles. The most common catalyst is sodium hydroxide, though lithium, potassium, magnesium, calcium, strontium, and barium hydroxides or oxides are also frequently used. Amine catalysis is also common. Occasionally, a Lewis acid salt, such as zinc acetate or tin chloride will be used to achieve some special property. Due to inclusion of excess aldehyde, resoles are capable of curing without addition of methylene donors. Although cure accelerators are available, it is common to cure resoles by application of heat alone. 

In 1794 the Finnish chemist J. Gadolin, while examining a mineral that had recently been discovered in a quarry at Ytterby, near Stockholm, isolated what he thought was a new oxide (or earth ) which A. G. Ekeberg in 1797 named yttria. In fact it was a mixture of a number of metal oxides from which yttrium oxide was separated by C. G. Mosander in 1843. This is actually part of the fascinating story of the rare earths to which we shall return in Chapter 30. The first sample of yttrium metal, albeit very impure, was obtained by F. Wohler in 1828 by the reduction of the trichloride by potassium. 

In 1789 M. H. Klaproth examined pitchblende, thought at the time to be a mixed oxide ore of zinc, iron and tungsten, and showed that it contained a new element which he named uranium after the recendy discovered planet, Uranus. Then in 1828 J. J. Berzelius obtained an oxide, from a Norwegian ore now known as thorite he named this thoria after the Scandinavian god of war and, by reduction of its tetrachloride with potassium, isolated the metal thorium. The same method was subsequendy used in 1841 by B. Peligot to effect the first preparation of metallic uranium. 

When the terpene a-fenchene (isopinene) is hydrated by means of acetic and sulphuric acids, it yields an isomer of fenchyl alcohol, which is known as isofenchyl alcohol (q.v.), and which on oxidation yields iso-fenchone, as fenchyl alcohol yields fenchone. The two ketones, fenchone and isofenchone, are sharply differentiated by isofenchone yielding iso-fenchocamphoric acid, Cj Hj O, on oxidation with potassium permanganate, which is not the case with fenchone. According to Aschan,i the hydrocarbon found in turpentine oil, and known as /9-pinolene (or cyclo-fenchene—as he now proposes to name it), when hydrated in the usual manner, yields both fenchyl and isofenchyl alcohols, which on oxidation yield the ketones fenchone and isofenchone. According to Aschan the relationships of these bodies are expressed by the following formulae —... 

Lithium forms the following compounds lithium oxide, LiaO lithium hydroxide, LiOH lithium sulfide, Li2S. Name and write the formulas of the corresponding sodium and potassium compounds. 

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