Ferrous salt

Absolute diethyl ether. The chief impurities in commercial ether (sp. gr. 0- 720) are water, ethyl alcohol, and, in samples which have been exposed to the air and light for some time, ethyl peroxide. The presence of peroxides may be detected either by the liberation of iodine (brown colouration or blue colouration with starch solution) when a small sample is shaken with an equal volume of 2 per cent, potassium iodide solution and a few drops of dilute hydrochloric acid, or by carrying out the perchromio acid test of inorganic analysis with potassium dichromate solution acidified with dilute sulphuric acid. The peroxides may be removed by shaking with a concentrated solution of a ferrous salt, say, 6-10 g. of ferrous salt (s 10-20 ml. of the prepared concentrated solution) to 1 litre of ether. The concentrated solution of ferrous salt is prepared either from 60 g. of crystallised ferrous sulphate, 6 ml. of concentrated sulphuric acid and 110 ml. of water or from 100 g. of crystallised ferrous chloride, 42 ml. of concentrated hydiochloric acid and 85 ml. of water. Peroxides may also be removed by shaking with an aqueous solution of sodium sulphite (for the removal with stannous chloride, see Section VI,12). 

Di-teo-propyl ether. The commercial product usually contains appreciable quantities of peroxides these should be removed by treatment with an acidified solution of a ferrous salt or with a solution of sodium sulphite (see under Diethyl ether). The ether is then dried with anhydrous calcium chloride and distilled. Pure di-iao-propyl ether has b.p. 68-5°/760 mm. 

Upon boiling the alkaline ferrous salt solution, some ferric ions are inevitably produced by the action of the air upon the addition of dilute siilphurio acid, thus dissolving the ferrous and ferric hydroxides, the ferrocyanides reacts with the ferric salt producing ferric ferrocyanide (Prussian blue) ... 

Glycohc acid also undergoes reduction or hydrogenation with certain metals to form acetic acid, and oxidation by hydrogen peroxide ia the presence of ferrous salts to form glyoxylic acid [298-12A], HCOCOOH, and ia the presence of ferric salts ia neutral solution to form oxaHc acid, HOOCCOOH formic acid, HCOOH and Hberate CO2 and H2O. These reduction and oxidation reactions are not commercially significant. 

Rea.ctlons, When free (R-R, R -tartaric acid (4) is heated above its melting point, amorphous anhydrides are formed which, on boiling with water, regenerate the acid. Further heating causes simultaneous formation of pymvic acid, CH COCOOH pyrotartaric acid, HOOCCH2CH(CH2)COOH and, finally, a black, charred residue. In the presence of a ferrous salt and hydrogen peroxide, dihydroxymaleic acid [526-84-1] (7) is formed. Nitrating the acid yields a dinitro ester which, on hydrolysis, is converted to dihydroxytartaric acid [617 8-1] (8), which upon further oxidation yields tartronic acid [80-69-3] (9). 

Iron oxide yellows can also be produced by the direct hydrolysis of various ferric solutions with alkahes such as NaOH, Ca(OH)2, and NH. To make this process economical, ferric solutions are prepared by the oxidation of ferrous salts, eg, ferrous chloride and sulfate, that are available as waste from metallurgical operations. The produced precipitate is washed, separated by sedimentation, and dried at about 120°C. Pigments prepared by this method have lower coverage, and because of their high surface area have a high oil absorption. 

Transparent yeUow pigment is composed of needle particles of EeO(OH) having a thickness of 2—5 nm, a width of 10—20 nm, and a length of 50—100 nm. They are prepared by the precipitation process from a very diluted solution of ferrous salt, eg, 6 wt % ferrous sulfate, foUowed by the oxidation of the precipitate with atmospheric oxygen at a temperature of less than 25°C. The precipitate is left to mature for about one day, then filtered, dried, and milled. 

The PGM concentrate is attacked with aqua regia to dissolve gold, platinum, and palladium. The more insoluble metals, iridium, rhodium, mthenium, and osmium remain as a residue. Gold is recovered from the aqua regia solution either by reduction to the metallic form with ferrous salts or by solvent-extraction methods. The solution is then treated with ammonium chloride to produce a precipitate of ammonium hexachloroplatinate(IV),... 

Acid. The reaction requires only enough acid to generate the ferrous ion which is needed to participate in the first step. Alternatively, a ferrous salt can be added directiy. Generally 0.05 to 0.2 equivalents of either hydrochloric or sulfuric acid is used, but both acids have their drawbacks. Hydrochloric acid can cause the formation of chlorinated amines and sulfuric acid can cause the rearrangement of intermediate aryUiydroxylamines to form hydroxyaryl amines. Occasionally an organic carboxyUc acid such as acetic or formic acid is used when there is a danger of hydrolysis products being formed. 

Neutral or alkaline salts, eg, KCl, K SO, K CO, or Na PO, are often present in synthetic latices in quantities of - <1%, based on the weight of the mbber. During emulsion polymerization the salts help control viscosity of the latex and, in the case of alkaline salts, the pH of the system. Many polymerizations are carried out at high pH, requiring the use of fixed alkaH, eg, KOH or NaOH. Very small amounts of ferrous salts can be employed as a component of the initiator system, in which case a sequesteriag agent, eg, ethyldiaminotetraacetic acid (EDTA) may be iacluded to complex the iron. Water-soluble shortstops, eg, potassium dithiocarbamate, may also be iacluded ia very small amounts (ca 0.1 parts). 

The most suitable oxidizing agent is potassium ferricyanide, but ferric chloride, hydrogen peroxide ia the presence of ferrous salts, ammonium persulfate, lead dioxide, lead tetraacetate or chromate, or silver and cupric salts may be useful. Water mixed, eg, with methanol, dimethylformamide, or glycol ethers, is employed as reaction medium. 

The yellow oxides are prepared by precipitating hydrated ferric oxide from a ferrous salt usiag an alkaU, followed by oxidation. The shades obtained range from light lemon yellow to orange, depending on the conditions used for the precipitation and oxidation. Yellow oxides contain about 85% Fe202 and 15% water of hydration. 

Other pharmaceutical chemicals such as calcium gluconate, ferrous salts, nikethamide, glycerophosphates, chloral hydrate, saccharin, antihistamines (including meclozine, and buclozine), tranquilizers (including meprobamate and chloropromazine), antifilarials, diethylcarbamazine citrate, and oral antidiabetics, including tolbutamide and chloropropamide ... 

Two other methods worth discussing are wet air oxidation and regeneration by steam. Wet oxidation may be defined as a process in which a substance in aqueous solution or suspension is oxidized by oxygen transferred from a gas phase in intimate contact with the liquid phase. The substance may be organic or inorganic in nature. In this broad definition, both the well known oxidation of ferrous salts to ferric salts by exposure of a solution to air at room temperature and the adsorption of oxygen by alkaline pyrogallol in the classical Orsat gas analysis would be considered wet oxidations. 

Chemical Designations - Synonyms Ferrous oxalate dihydrate, Ferrox, Iron protoxalate. Oxalic acid (ferrous salt) Chemical Eormula FeC204 2H20. 

Ferrous ammonium sulfate, 68 Ferrous cliloride, 68 Ferrous ferrite, 69 Ferrous salts, 69 Ferrous sulfate, 69 Fesil Group ASA, 196 Fibrous glass, 69... 

Fission of the Oxazirane Ring with Ferrous Salts... 

A direct attack on the oxazirane ring occurs with ferrous salts. Oxaziranes are decomposed by aqueous solutions of ferrous ammonium sulfate even at room temperature. The reaction follows a radical-chain mechanism because le.ss than stoichiometric amounts of the ferrous salt cause the decomposition, 2-icrt-Butyl-3-phenyloxazirane (9) and 1 equivalent of ferrous salt give ferf-butylbenzamide in 98%... 

Oxaziranes derived from isobutyraldehyde react with ferrous salts to give only substituted formamides fEq. (23)], The chain propagating radical 30 thus suffers fission with elimination of the isopropyl group. An H-transfer would lead to substituted butyramides, which are not found. Here is seen a parallel to the fragmentation of alkoxyl radicals, where the elimination of an alkyl group is also favored over hydrogen. The formulation of the oxazirane fission by a radical mechanism is thus supported. 

The composition of the products is reminiscent of the decomposition of the trialkyl-oxaziranes by ferrous salts. Here also the nitrogen atom is dealkylated and the carbon atom of the oxazirane ring is found as a ketone group. 

The mechanism proposed by Emmons thus corresponds in part to the decomposition of the trialkyl-oxaziranes by ferrous salts. By radical attack on the 7V-alkyl group of the oxazirane, the radical 32 is formed which rearranges with ring opening to 33. Radical 33 propagates the chain by attack on a further molecule of oxazirane. It takes up an H-atom and is decomposed to ketone and ammonia. The aldehyde produced from the M-alkyl group is converted to tar. 

Eisenoxydul-hydrat, n. ferrous hydroxide, iron(ll) hydroxide, -oxyd, n. ferrosoferric oxide, iron(II,III) oxide, magnetic iron oxide (FeaOi). -salz, n. ferrous salt, iron(II) salt, -sulfat, n. ferrous sulfate, iron(II) sulfate, -verbindung, /. ferrous compound, iron(ll) compound. 

Reduction of unsaturated carbonyl compounds to the saturated carbonyl is achieved readily and in high yield. Over palladium the reduction will come to a near halt except under vigorous conditions (73). If an aryl carbonyl compound, or a vinylogous aryl carbonyl, such as in cinnamaldehyde is employed, some reduction of the carbonyl may occur as well. Carbonyl reduction can be diminished or stopped completely by addition of small amounts of potassium acetate (i5) to palladium catalysts. Other effective inhibitors are ferrous salts, such asferroussulfate, at a level of about one atom of iron per atom of palladium. The ferrous salt can be simply added to the hydrogenation solution (94). Homogeneous catalysts are not very effective in hydrogenation of unsaturated aldehydes because of the tendencies of these catalysts to promote decarbonylation. 

The inspector s working standard for the surface finish of blast-cleaned steel is now the new British Standard . In the special circumstances where absolute freedom from soluble contaminants such as ferrous sulphate is necessary, the specification should include reference to a test for removal of such residual salts, e.g. the potassium ferricyanide test . The area to be sampled should be wetted with a fine spray of distilled water and the paper held against it. The development of blue spots on the paper indicates the presence of ferrous salts on the surface. 

Higher homologs tend to hydrolyze to original aldehyde redn to carbonyl and hydroxy compds ferrous salts catalyze decompn to free radicals thermal decompn involves homolytic and hetero-... 

Highly expl decompd by ferrous salts, Ag, Pd and Pt stable in storage distillable under vacuum... 

Note According to Thrope (Ref 3), the anhydr ferrous salt is very sensitive in 1901, it caused a fire at Huddersfield... 

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