Ferric oxide hydrated

The Penniman-Zoph process involves the preparation of seeds or nucleating particles by the alkaU precipitation of ferrous sulfate. The reaction is carried out at alow temperature using an excess of ferrous ions. The hydroxide is then oxidized to the seeds of hydrated ferric oxide ... 

Iron Browns. Iron browns are often prepared by blending red, yellow, and black synthetic iron oxides to the desired shade. The most effective mixing can be achieved by blending iron oxide pastes, rather than dry powders. After mixing, the paste has to be dried at temperatures around 100°C, as higher temperatures might result in the decomposition of the temperature-sensitive iron yellows and blacks. Iron browns can also be prepared directiy by heating hydrated ferric oxides in the presence of phosphoric acid, or alkaU phosphates, under atmospheric or increased pressure. The products of precipitation processes, ie, the yellows, blacks, and browns, can also be calcined to reds and browns. 

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. 

Supporting the hydrated ferric oxide chips is a combination of a perforated, heavy metal support plate and a coarse support packing material. This material may consist of scrap pipe thread protectors and 2-3-in. sections of small diameter pipe. This provides support for the bed, while offering some protection against detrimental pressure surges. 

The product, ferrous hydroxide, is commonly further oxidised to magnetite (Fej04) or a hydrated ferric oxide (FeOOH), i.e. rust. 

In rusting, the initial corrosion product of iron is ferrous hydroxide. Reacting with oxygen and water, it forms higher oxides, mainly hydrated ferric oxide and magnetite. Rust formed in industrial or marine environments contains corrosion-promoting salts and is particularly dangerous. Rust is not considered a satisfactory base over which to paint and it too must be removed. 

For steel, passivation is achieved by the surface formation of a tough, adherent mixture of oxides. The passive film is primarily gamma-magnetite (y-Fe203) but also contains gamma-hydrated ferric oxide (y-FeOOH). The film thickness is perhaps 15 A to 30 A (angstrom units). 

In the goethite process, the precipitation of iron from solution occurs in the form of hydrated ferric oxide, FeOOH. The commercial development of the process was due to Societe de La Vielle Montagne. The process basically involves the reduction of iron to the ferrous state, and this is followed by oxidation by air at a temperature of around 90 °C and at a pH controlled at around 3.0. The reaction can chemically be shown as ... 

The core of the iron storage protein ferritin consists of a hydrated ferric oxide-phosphate complex. Various models have been proposed which feature Fe111 06 oct., Fe111 O4 tet. or Fe111 O4 tet. Fe111 06 oct. complexing the first listed is preferred by Gray (99) on the basis of the electronic absorption spectrum. The protein very closely related to ferritin which occurs in the mold Phycomyces blakesleeanus contains... 

Penniman-Zoph A process for making a yellow iron oxide pigment. Hydrated ferric oxide seed is added to a solution of ferrous sulfate and the suspension circulated over scrap iron, with air being passed through. Hydrated ferric oxide deposits on the seed crystals, giving a finely divided, yellow pigment ... 

Typically, mammalian ferritins can store up to 4500 atoms of iron in a water-soluble, nontoxic, bioavailable form as a hydrated ferric oxide mineral core with variable amounts of phosphate. The iron cores of mammalian ferritins are ferrihydrite-like (5Fe203 -9H20) with varying degrees of crystallinity, whereas those from bacterioferritins are amorphous due to their high phosphate content. The Fe/phosphate ratio in bacterioferritins can range from 1 1 to 1 2, while the corresponding ratio in mammalian ferritins is approximately 1 0.1. 

To the best of our knowledge, there is one host which conforms to the structure of an Archimedean dual. Harrison was the first to point out that the quaternary structure of ferritin, a major iron storage protein in animals, bacteria, and plants, corresponds to the structure of a rhombic dodecahedron. [45] This protein, which is approximately 12.5 nm in diameter, consists of 24 identical polypeptide subunits (Fig. 9.18), and holds up to 4500 iron atoms in the form of hydrated ferric oxide with... 

Both humic acids and fulvic acids have a strong affinity for particulate and crystalline substances possessing oxygen atoms at their surfaces and they have been reported to bring about the dissolution of iron phosphate, calcium phosphate (61), uranium dioxide (65), hydrated magnesium alumino-silicates (66) and limonite, a complex mixture of hydrated ferric oxides (67). 

After lapse of time, the hydrated ferric oxide ceases to have any sulphuretted hydrogen-absorbing power, so the gas is diverted through other hydrated oxide, and the spent oxide removed and placed in the open air, when, after moistening with water and exposure, the following reaction takes place.—... 

In ordinary commercial purification of water gas, 100 tons of hydrated ferric oxide will effectively purify 200,000 cubic feet of crude water gas per 24 hours this allows of keeping 20-30 tons of revivified oxide in reserve, available to replace the working oxide as it becomes spent . 

III) Methylamlne In water reacts with ferric chloride to precipitate hydrated ferric oxide. 

It oxidizes slowly in the atmosphere, eventually forming the reddish-hrown hydrated ferric oxide, Fe203 nH20. 

Metastability of Hydrolyzed Iron (III) Solutions The low solubility of ferric hydroxide has been alluded to in the Introduction. Feitknecht and Michaelis (29) have observed that aU ferric perchlorate solutions to which base has been added are unstable with respect to eventual precipitation of various forms of hydrated ferric oxides. In 3 M NaC104 at 25° C the two phase system reaches an apparent equilibrium after 200 hours, according to Biedermann and Schindler (6), who obtained a reproducible solubility product constant for ferric hydroxide at varying degrees of hydrolysis. It appears that many of the solutions used in the equilibrium studies of Hedstrom (9) and Biedermann (22) were metastable, and should eventually have produced precipitates. Nevertheless, since the measured potentials were reversible, the conclusions reached about the species present in solution remain valid. 

Insol in w, ale. or eth sol In acids occurs in nature as mineral magnetite. Can be prepd in pure state by dehydrating pptd hydrated ferric oxide, followed by reduction with hydrogen. 

Within tissues of animals, plants, and fungi much of the iron is packaged into the red-brown water-soluble protein ferritin, which stores Fe(III) in a soluble, nontoxic, and readily available form.61 64 Although bacteria store very little iron,65 some of them also contain a type of ferritin.66-67 On the other hand, the yeast S. cerevisieae stores iron in polyphosphate-rich granules, even though a ferritin is also present.65 Ferritin contains 17-23% iron as a dense core of hydrated ferric oxide 7 nm in diameter surrounded by a protein coat made up of twenty-four subunits of mo-... 

If a soap is added to a lead hydrogen arsenate-hydrated ferric oxide mixture considerable damage and leaf drop is caused, especially if the soap contains a strong base, as in the case of commercial potash fish-oil soap or potassium oleate. Laboratory tests show that more soluble arsenic is formed than with a soap of a weak base such as triethanolamine oleate.7 The addition of cryolite to an arsenate inhibits the formation of soluble arsenic 8 fluosilicates cause decomposition. These fluorine... 

SSzni of coneentrated aqueous ammonia is added with stir-ring. When the hydrated ferric oxide settles well, most of the supernatant liquid is carefully decanted, and the precipitate is filtered off and washed several times with boiling water. 

Yellow ochres are earths composed essentially of clay coloured by hydrated ferric oxide they may contain siliceous sand, calcium carbonate, small proportions of manganese oxides, and sometimes basic ferric sulphate and calcium and barium sulphates. Chalk, gypsum and heavy spar may be added fraudulently and the colour may be " improved by artificial organic dyes, vegetable colours or chrome yellow. 

An artificial pigment analogous to the ochres is Mars yellow, consisting of a mixture of hydrated ferric oxide with calcium sulphate, alumina or zinc oxide of analogous composition are the pigments derived from it by more or less pronounced heating (Mars orange, red, brown, violet, purple). 

This is a variety of ochre containing large proportions of hydrated ferric oxide and oxides of manganese and also small quantities of humous substances. 

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