Fluorides borates

Sulfate The coprecipitation of relatively few anions with carbonate minerals has been studied and, with the exception of sulfate, these studies have generally not been as detailed as many of those with cations. However, coprecipitation reactions can be important for the removal of ions such as fluoride, borate, and phosphate from seawater (e.g., Morse and Cook, 1978 Okumura et al., 1983). It is also probable that anions will eventually gain a greater stature in the study of diagenesis... 

This section will discuss insecticides, acaricides, and repellents having toxicological characteristics distinct from the insecticides discussed in the previous section. It discusses pyrethroids, fluorides, borates, chlordimeform, propargite, substituted haloaromatic urea compounds, chlorobenzilate, cyhexa-tin, methoprene, sulfur, diethyltoluamide, aUcyl phthalates, and benzyl benzoate. 

In food, drinking water and drinks there are numerous inorganic anions. Some anions are forms of organogenic elements (such as carbonates and hydrogen carbonates), of essential elements (chlorides, phosphates, sulfates, iodides, fluorides, borates) and of non-essential elements (bromides). These and many other anions are mostly beneficial or harmless, and toxic effects exhibit only if present in food, drinking water and drinks in large quantities. Toxic effects can also result from an excessive accidental intake of these anions (fluorides, iodides and bromides). 

Uses. Lithium fluoride is used primarily in the ceramic industry to reduce firing temperatures and improve resistance to thermal shock, abrasion, and acid attack (see Ceramics). Another use of LiF is in flux compositions with other fluorides, chlorides, and borates for metal joining (17) (see Solders). 

The presence of inorganic salts may enhance or depress the aqueous solubiUty of boric acid it is increased by potassium chloride as well as by potassium or sodium sulfate but decreased by lithium and sodium chlorides. Basic anions and other nucleophiles, notably borates and fluoride, greatly increase boric acid solubihty by forrning polyions (44). 

A large number of electrolytic treatments of magnesium, anodic or a.c., have been developed, in which adherent white or grey films consisting of fluoride, oxide, hydroxide, aluminate or basic carbonate are deposited from alkaline solutions containing caustic alkali, alkali carbonates, phosphates, pyrophosphates, cyanides, aluminates, oxalates, silicates, borates, etc. Some films are thin, and some are relatively thick. All are more or less absorbent and act as good bases for paint, though none contributes appreciable inhibition. All can, however, absorb chromates with consequent improvement of protective efficiency. 

Phosphate, arsenate, and vanadate interfere. Borate, fluoride, and large amounts of aluminium, calcium, magnesium, and the alkali metals have no effect in the determination, but large amounts of iron (> 5 per cent) appear to produce slightly low results. 

In 1888, Turpin prepd a series of cool expls which were permissable, by incorporating materials such as alkali chlorides, Na or K bicarbonate (up to 50% content), fluorides, acetates, oxalates, Ba carbonate. 10H2O, chromates, hyposulfites, stannic acid, boric acid, borates, etc, in the expls listed above eg, a) K chiorate 45, double salt of Ca and K acetochlorate 35, tar 18, charcoal 5, and alkali bicarbonate or oxalate I5ps b) K chlorate 15, double salt of K and Amm chlorobichromate 35 K or Na nitrate 10, tar 18, charcoal 5, and K or Na bicarbonate 15ps... 

Aluminium borohydride Aluminium chloride Aluminium chlorate Ammonium tetrachloroaluminate Aluminium fluoride Aluminium trihydroxide Aluminium ammonium sulphate Aluminium potassium sulphate Aluminium nitride Aluminium nitrate Sodium aluminate Aluminium sodium aluminate Aluminium phosphate Aluminium phosphide Aluminium borate Aluminium oxychloride Aluminium fluorosilicate Aluminium magnesium silicate Aluminium sulphate... 

The most general method for the simultaneous analysis of oxyanions by gas chromatography is the formation of trimethylsilyl derivatives. Trimethylsilyl derivatives of silicate, carbonate, oxalate, borate, phosphite, phosphate, orthophosphate, arsenite, arsenate, sulfate and vanadate, usually as their ammonium salts, are readily prepared by reaction with BSTFA-TMCS (99 1). Fluoride can be derivatized in aqueous solution with triethylchlorosilane and the triethylfluorosilane formed extracted into an immiscible organic solvent for analysis by gas chromatography [685). 

These rod-shaped ligands share a sterically efficient terminal N-donor and their divalent Co chemistry is well established. They will be discussed here only with selected examples. [Co (NCMe)6](TFPB)2 (TFPB- = tetrakis(3,5-bis(trifhioromethyl)phenyl)borate)) has been synthesized and characterized in the solid state along with a number of other divalent transition metal analogs.357 As a result of the extremely poor coordinating ability of the anion and facile loss of MeCN ligands from the cation, the salt is an excellent source of naked Co2+ ions. Thermolysis up to 100 °C leads to the loss of one MeCN and formation of a r -bound nitrile, whereas above 130 °C decomposition occurs with loss of MeCN and abstraction of fluoride from the anion to form CoF2. 

A further spectrophotometric method [3, 4] for water soluble boron in soil, boron is extracted from soil with boiling water. Borate in the extract is converted to fluoroborate by the action of orthophosphoric acid and sodium fluoride. The concentration of fluoroborate is measured spectrophotometrically as the blue complex formed with methylene blue and which is extracted into 1, 2-dichloroethane. Nitrates and nitrites interfere they are removed by reduction with zinc powder and orthophosphoric acid. 

Thus, heptafulvalene (522) was isolated in 33 and 65% yield after thermolysis of 517 in diglyme and its photolysis in THF, respectively [193]. An almost quantitative yield of 522 resulted when a mixture of 1-, 2- and 3-chloro-l,3,5-cycloheptatriene (518a) was treated with KOtBu in THF [206]. Even on variation ofthe concentration of the starting material and the temperature of the reaction, 522 turned out to be the exclusive product [207]. Also, the treatment of (trimethylsilyl)tropylium tetrafluoro-borate (519) with tetrabutylammonium fluoride [208] and the gas-phase pyrolysis of 7-acetoxynorbornadiene and 7-acetoxy-l,3,5-cycloheptatriene [209] afforded high yields of 522. Further, 522 was observed on FVT of N-nitroso-N-(7-norbornadienyl)-urea at 350 °C, which is believed to be converted into 7-diazonorbornadiene initially. Its decomposition should proceed via 7-norbornadienylidene to bicyclo[3.2.0]hepta-l(2),3,6,-triene (514) (Scheme 6.103) and then on to 5 [210]. The intermediacy of 514 is also suspected in the formation of 522 from 7-acetoxynorbornadiene. 

Borides The electrolysis (at 950-1100°C) of a mixture of a borate and a transition metal fluoride (or alkaline-earth fluoride with the transition metal oxide) resulted in the synthesis of several borides (Ca, Sr, Y, Th, Ti, V, etc.). 

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