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Iron salt

The reaction mechanism for these products is not clearly understood, but the introduction of organo-metallic compounds (barium or iron salts in colloidal suspension) has been shown to have a beneficiai action on the combustion of diesel fuel in engines and reduce smoke. However, these products cause deposits to form because they are used in relatively large proportions (on the order 0.6 to 0.8 weight %) to be effective. [Pg.353]

The hammer and the surface on which the lithium is flattened should be free from rust traces of iron salts may cause rapid decomposition of the alkyllithium. [Pg.12]

Kota 1. If more than 100 mg of the iron salt is used as catalyst for the conversion of lithium, the separation of the layers during the work-up may be difficult, owing to the formation of iron hydroxide gel. [Pg.108]

Salicylic acid Iodine, iron salts, lead acetate... [Pg.1212]

Iron (III) chloride hexahydrate [10025-77-17, FeCl36H2 0, is a brown-yeUow to orange material that crystallizes from a solution of iron or iron salt dissolved ia hydrochloric acid that coataias an oxidant such as Cfy or nitric acid. The monoclinic crystals contain the complex salt... [Pg.436]

Most iron salts and compounds may be safely handled following common safe laboratory practices. Some compounds are irritants. A more serious threat is ingestion of massive quantities of iron salts which results in diarrhea, hemorrhage, fiver damage, heart damage, and shock. A lethal dose is 200 250 mg/kg of body weight. The majority of the victims of iron poisoning are children under five years of age. [Pg.444]

Hydroperoxides are generally used with reducing agents, eg, iron salts, in redox emulsion polymerization systems. [Pg.134]

In the direct precipitation process, the seeds of iron(III) oxide are added to an iron salt solution, most often iron(II) sulfate, which is subsequendy oxidized by air. The released sulfuric acid is removed by the addition of metallic iron with which it reacts to iron(II) sulfate. The overall reaction shows that ferrous sulfate is not consumed during the process. It only helps to oxidize metallic iron to ferric oxide ... [Pg.12]

Transparent red iron oxide is composed mainly of hematite, a-Ee202, having primary particles about 10 nm. It is prepared by a precipitation reaction from a dilute solution of an iron salt at a temperature around 30°C, foUowed by a complete oxidation in the presence of some seeding additives,... [Pg.16]

Tolypomycins. The addition of small amounts of iron salts to the fermentation medium increases the production of tolypomycin Y (48) (7,203,204), the stmcture of which was arrived at by chemical degradation (205,206) and confirmed by x-ray crystallographic analysis (207) (Fig. 5). Mild acid hydrolysis of tolypomycin Y yields tolypomycinone [22356-23-6] (49, R = H), C27H42NO23, and tolyposamine [34174-76-0] C23H23NO2, (50). Further hydrolysis of tolypomycinone using acid yields tolyponone [24317-12-2] (51), which is also formed upon mild acid hydrolysis of rifamycia S. [Pg.499]

In a variation of this method, isolation of the ben2hydrol derivative is not required. The methane base undergoes oxidative condensation in the presence of acid with the same or a different arylamine direcdy to the dye. New fuchsine [3248-91 -7] Cl Basic Violet 2 (16), is prepared by condensation of two moles of o-toluidine with formaldehyde in nitrobenzene in the presence of iron salts to give the corresponding substituted diphenylmethane base. This base is also not isolated, but undergoes an oxidative condensation with another mole of o-toluidine to produce the dye. [Pg.272]

The treatment units used for color removal are the same as those used for turbidity removal. However, the pH must be increased prior to filtration so that the metal hydroxides are removed by the filters. At low pH values, metal ions or their soluble complexes readily pass through the filters and form insoluble species in storage tanks and in the distribution system. For iron salts, it is important that the pH be greater than 6 as the oxidation of iron(II) to iron(III) occurs rapidly above this pH in the presence of dissolved oxygen or other strong oxidants (18). [Pg.278]

Once the green, nonalum modifications of the chromium ion have formed, reversion to the hexaaquo form on cooling is sufficiendy slow that on chilling to 5°C a cmde ferrous ammonium sulfate can be crystallised, removing neady all the iron from the system. This cmde iron salt is treated with makeup ammonium sulfate, heated again to retain the chromium impurities in the green noncrystallisahle form, and then cooled to separate the bulk of the iron as a technical ferrous ammonium sulfate, which is sold for fertiliser and other purposes. The mother Hquor from this crystallisation is returned to the filtration step. [Pg.117]

Brown oxides are manufactured either by blending mixtures of the red, yellow, and black oxides or by precipitation of an iron salt with alkaU followed by partial oxidation of the precipitate. The result is a mixture of red Fe202 [1309-37-1] and black Fe O [1309-38-2] FeO Fe202-... [Pg.452]

One method of generating hydroxyl radicals is by a dding a soluble iron salt to an acid solution of hydrogen peroxide (Fenton s reagent) (176—180), ie ... [Pg.383]

Chemical precipitation can remove 95 percent of the suspended solids, up to 50 percent of the soluble organics and the bulk of the heavy metals in a wastewater. Removal of soluble organics is a function of the coagulant chemical, with iron salts yielding best results and lime the poorest. Metal removal is primarily a function of pH and the ionic state of the metal. Guidance is available from solubihty product data. [Pg.2215]

Deposits contained organic acids formed by oxidation of rolling oils. Up to 40% by weight of the lumps shown in Fig. 4.27A and B was iron oxides, hydroxides, and organic-acid iron salts. Acidic species concentrated in the deposits. [Pg.91]


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