Manganese salt

The Mn-salt/bicarbonate system is also catalytically active in ionic hquids. Epoxidation of a range of alkenes with 30% aqueous H2O2 can be accomphshed with 

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Oxidation of manganese dioxide to higher valence states takes place in the fusion process of Mn02 and KOH. A tetravalent manganese salt identified as K MnO [12142-27-7] (63) which disproportionates spontaneously is formed. 

Unsymmetrical dialkyl peroxides are obtained by the reaction of alkyl hydroperoxides with a substrate, ie, R H, from which a hydrogen can be abstracted readily in the presence of certain cobalt, copper, or manganese salts (eq. 30). However, this process is not efficient since two moles of the hydroperoxide are consumed per mole of dialkyl peroxide produced. In addition, side reactions involving free radicals produce undesired by-products (44,66). 

The manganese salt (M = Mn), ie, manganese 2B (PR 48 4) is a bluish red, characteri2ed by superior masstone lightfastness and outdoor durabiUty, and finds use in some automotive and other high quaUty industrial finishes. It is also used in some plastics, because of reasonably good heat stabiUty, and a variety of printing inks. 

Branched-chain acids have a wide variety of industrial uses as paint driers (7), vinyl stabilizers (8), and cosmetic products (9). Cobalt and manganese salts of 2-ethyIhexanoic acid and neodecanoic acid are used as driers for paint, varnishes, and enamels litbium, magnesium, calcium, and aluminum salts of 2-ethyIhexanoic acid are used in the formation of greases and lubricants (see Driers and metallic soaps). Derivatives of isostearic acid have been used as pour point depressants in two-cycle engine oils, as textile lubricants, and in cosmetic formulations. Further industrial appHcations can be found (10). 

Monoazo Pigments. In combination with other groups, the a2o linkage, —N=N—, imparts color to many dyes and pigments (see Azo Dyes). The simplest of these, ie, the Hansa yellows, toluidine reds, and naphthol reds, do not have the lightfastness and heat stabiUty required for plastics. Permanent YeUow FGL and Permanent Red 2B are stable enough for vinyls, polyethylene, polypropylene, and ceUulosics (11). Permanent Red 2B is available as the calcium, barium, or manganese salt. 

The EBDCs are prepared by reaction of EDA with carbon disulfide in the presence of sodium or ammonium hydroxide initially, then with 2inc and/or manganese salts, as appropriate (156—160). A continuous process has recendy been reported (161). The common names of these salts are nabam [142-59-6] (Na salt), amobam (ammonium salt), 2ineb [12122-67-7] (Zn salt), maneb [12427-38-2] (Mn salt), andmanco2eb. 

Terephthalic acid is made by air oxidation of /i-xylene in acetic acid with cobalt and manganese salts of metal bromide at 200 °C and 400 tit. 

Mangan-reserve, /. (Calico) manganese resist, -salz, n. manganese salt. 

The catalytic oxidation of long-chain paraffins (C18-C30) over manganese salts produces a mixture of fatty acids with different chain lengths. Temperature and pressure ranges of 105-120°C and 15-60 atmospheres are used. About 60 wt% yield of fatty acids in the range of C12-C14 is obtained. These acids are used for making soaps. The main source for fatty acids for soap manufacture, however, is the hydrolysis of fats and oils (a nonpetroleum source). Oxidation of paraffins to fatty acids may be illustrated as ... 

Iron salts (and to a lesser extent manganese salts) are found in many surface water supplies and industrial water. Both ferrous (Fe2+) and ferric (Fe3+) iron may be present in the water, depending on the pH. 

Aeration towers are often simply constructed wooden towers with or without the benefit of a forced-air draft, over which the well water is distributed. Typically, the tower holds 8 to 10 trays, each with a 3- to 4-inch (7.6-10.2 cm) bed depth of volcanic lava or coke media to provide the total 30 to 36" (76-91 cm) depth required. The lava or coke acts as a catalyst for the further precipitation of iron and manganese salts. These salts can be readily oxidized provided there is sufficient alkalinity present. If in doubt, ensure a minimum of 120 to 150 ppm total alkalinity (T Aik or M Aik) as CaC03. 

The paraffin wax is oxidized by air in a liquid phase process at 110-130°C. Catalysts for this radical reaction are cobalt or manganese salts [54]. The quality of the obtained mixture of homologous carboxylic acids is impaired by numerous byproducts such as aldehydes, ketones, lactones, esters, dicarboxylic acids, and other compounds. These are formed despite a partial conversion of the paraffin and necessitate an expensive workup of the reaction product [50,55]. 

Addition of phosphonyl radicals onto alkenes or alkynes has been known since the sixties [14]. Nevertheless, because of the interest in organic synthesis and in the initiation of free radical polymerizations [15], the modes of generation of phosphonyl radicals [16] and their addition rate constants onto alkenes [9,12,17] has continued to be intensively studied over the last decade. Narasaka et al. [18] and Romakhin et al. [19] showed that phosphonyl radicals, generated either in the presence of manganese salts or anodically, add to alkenes with good yields. 

Rather than natural ores as in Leclanche batteries, electrolytic manganese dioxide (EMD), which is produced by anodic oxidation of Mn ions at graphite electrodes in solutions of manganese salts, is used as the active material for the positive... 

It is essential to mix thoroughly the spent oxidant and the silica gel with a spatula while washing. This process does not cause any manganese salt to pass into the filtrate. 

The variety of functions of the catalyst is pronounced, in particular, in the technological catalytic oxidation of -paraffins to aliphatic acids [5]. This technology consists of several stages among which the central place is occupied by oxidation. It is conducted at 380 420 K in a series of reactors, with a mixture of salts of aliphatic acids of K+ and Mn2+ or Na+ and Mn2+ as the catalyst. The alkaline metal salt stabilizes (makes it more soluble and stable) the manganese salt [152]. Studies have revealed the multifunctional role of the catalyst (manganese ions) (Mn) [152-154]. 

This reaction was studied in most detail by Narasaka and coworkers (313). These authors demonstrated that silyl nitronates can be oxidized by different triva-lent manganese salts (acetate, acetylacetonate, etc.), but Mn(pic)3 is the oxidizing agent of choice. 

Manganese salt tetrahydrate, Cl4HI0MnO4.4H2O, manganese benzoate. Pale-red powder. Sol in water, ale. Also occurs with 3H20. 

Likewise, the lightfastness of an azo pigment lake is controlled to a certain extent by the metal cation manganese salts are usually most lightfast. 

The term refers to azo colorants bearing sulfonic and/or carboxylic acid functions, which are used as pigments after being rendered insoluble by conversion into insoluble alkali earth or manganese salts. ... 

Diazotization of the aminosulfonic acid and subsequent coupling onto the sodium salt of 2-hydroxy-3-naphthoic acid initially affords the monoazo compound in the form of its soluble sodium salt. Subsequent reaction with chlorides or sulfates of alkaline earth metals or with a manganese salt, frequently in the presence of a dispersion agent, or rosin or its derivatives, at elevated temperature yields the insoluble BONA pigment lake. 

P.R.48 4, the manganese salt, affords red shades, which are noticeably on the bluish side of P.R.48 3 and yellower than P.R.48 2. The pigment is used in a variety of applications, especially in paints. In order to produce opaque shades of red, P.R.48 4 is frequently combined with Molybdate Orange. The pigment is considerably more lightfast and durable than other P.R.48 types, especially in full shades. 

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