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Iron-reducing agents

Several proteins that exist in food (e.g., lactoferrin, ferritin, transferritin, heme protein) possess strong binding sites for iron. Reducing agents (ascorbate, cysteine, superoxide anion) to low pH causes release of iron from proteins and accelerates lipid oxidation (34). Some amino acids and peptides found in muscle foods (e.g., carnosine) are capable of chelating metal ions and inhibit their prooxidant activity (35, 36). [Pg.482]

Special iron-reducing agents can be very effective in reducing or preventing add sludge formation in heavier oil reservoirs and can be considered for spedal applications. However, the iron control additives listed in table 6-8 are the most common and can be used for most applications encountered. [Pg.87]

High-temperature iron control (iron-reducing) agent... [Pg.128]

The alkali metal tetrahydridoborates are salts those of sodium and potassium are stable in aqueous solution, but yield hydrogen in the presence of a catalyst. They are excellent reducing agents, reducing for example ion(III) to iron(II). and silver ions to the metal their reducing power is used in organic chemistry, for example to reduce aldehydes to alcohols. They can undergo metathetic reactions to produce other borohydrides, for example... [Pg.147]

Reduction products vary depending on the reducing agent, for example dinitrogen oxide is obtained with sulphurous acid, nitrogen is obtained when the gas is passed over heated metals (e.g. copper and iron) and ammonia is produced when the gas reacts with aqueous chromiumfll) salts. [Pg.231]

In aqueous solution arsenic(lll) oxide is a reducing agent being oxidised to arsenate(V) by halogens, chlorate(I), nitric acid and even iron(III) chloride. [Pg.236]

In strongly acid solution, substances which are normally reducing agents reduce sulphur dioxide solution or sulphites, for example iron(II) and zinc ... [Pg.292]

The process of extraction requires first smelting (to obtain the crude metal) and then refining. In smelting, iron ore (usually an oxide) is mixed with coke and limestone and heated, and hot air (often enriched with oxygen) is blown in from beneath (in a blast furnace). At the lower, hotter part of the furnace, carbon monoxide is produced and this is the essential reducing agent. The reduction reactions occurring may be represented for simplicity as ... [Pg.391]

Iron is a good reducing agent (see the value just given) it... [Pg.392]

In this oxidation state, iron is quite readily oxidised by mild oxidising agents, and hence in many of the reactions it is a mild reducing agent. For acid conditions... [Pg.395]

On the technical scale, the cheaper iron and hydrochloric acid is employed as the reducing agent ... [Pg.559]

Iron(II) ediylenediaminetetraacetic acid [15651 -72-6] Fe(EDTA) or A/,Ar-l,2-ethaiiediylbis[A[-(carboxymethyl)glyciQato]ferrate(2—), is a colorless, air-sensitive anion. It is a good reducing agent, having E° = —0.1171, and has been used as a probe of outer sphere electron-transfer mechanisms. It can be prepared by addition of an equivalent amount of the disodium salt, Na2H2EDTA, to a solution of iron(II) in hydrochloric acid. Diammonium [56174-59-5] and disodium [14729-89-6] salts of Fe(EDTA) 2— are known. [Pg.439]

Reaction of free-base porphyrin compounds with iton(II) salts in an appropriate solvent results in loss of the two N—H protons and insertion of iron into the tetradentate porphyrin dianion ligand. Five-coordinate iton(III) porphyrin complexes (hemins), which usually have the anion of the iton(II) salt for the fifth or axial ligand, ate isolated if the reaction is carried out in the presence of air. Iron(II) porphyrin complexes (hemes) can be isolated if the reaction and workup is conducted under rigorously anaerobic conditions. Typically, however, iton(II) complexes are obtained from iton(III) porphyrin complexes by reduction with dithionite, thiolate, borohydtide, chromous ion, or other reducing agents. [Pg.441]

Colorimetric. A sensitive method for the deterrnination of small concentrations of dissolved iron is the spectrophotometric deterrnination of the orange-red tris(1,10-phenanthroline)iron (IT) complex. Other substituted phenanthrolines can be even more sensitive. Only the inon(II) complexes of these Ligands are highly colored. The sample is first treated with an excess of reducing agent. The complexes are stable from pH 2 ndash 9 and analysis preferably is done at about pH 3.5. [Pg.444]

Cementation. A metal can be removed from solution by displacing it with a mote active metal. This simple, inexpensive method has been commonly used to recover copper from dilute (1—3 kg/m ) solution using shredded iron and de-tinned iron cans as reducing agent. [Pg.171]

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

Miscellaneous. Chloroplatinic acid is used in the production of automobile catalysts. Platino-type prints based on reduction of Pt(II) to Pt(0) by a photosensitive reducing agent such as iron(III) oxalate are used in art photography (261,262). Infrared imaging devices based on a platinum siLicide detector have been developed (263). [Pg.185]


See other pages where Iron-reducing agents is mentioned: [Pg.520]    [Pg.191]    [Pg.390]    [Pg.334]    [Pg.84]    [Pg.85]    [Pg.84]    [Pg.85]    [Pg.520]    [Pg.191]    [Pg.390]    [Pg.334]    [Pg.84]    [Pg.85]    [Pg.84]    [Pg.85]    [Pg.101]    [Pg.107]    [Pg.111]    [Pg.223]    [Pg.232]    [Pg.628]    [Pg.11]    [Pg.278]    [Pg.279]    [Pg.283]    [Pg.366]    [Pg.438]    [Pg.440]    [Pg.68]    [Pg.506]    [Pg.167]    [Pg.169]    [Pg.384]    [Pg.539]    [Pg.539]    [Pg.89]   
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