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Oxidizing agent halogens

Alkali metals Moisture, acetylene, metal halides, ammonium salts, oxygen and oxidizing agents, halogens, carbon tetrachloride, carbon, carbon dioxide, carbon disul-flde, chloroform, chlorinated hydrocarbons, ethylene oxide, boric acid, sulfur, tellurium... [Pg.1207]

DUPLEX Disks extend corrosion resistance to highly oxidizing agents, halogens except free fluorine, and virtually all other corrosives. A sheet of PIPE is used as a barrier on the service side of the disk. See page 12. Additionally, these disks are processed to accommodate temperatures to 392E without insulation. [Pg.420]

When the temperature rises, polyphenylene sulfide can be attacked by hot strong acids and bases, chlorinated solvents, oxidizing agents, halogens, amines. For example, a given grade is unusable after a few months in 10% nitric acid at 90°C. After 1 year at 90°C in 37% hydrochloric acid, the retention of tensile strength is 29%. [Pg.552]

They are attacked by chlorine water, strong oxidizing agents, halogens, certain chlorinated solvents, amines... [Pg.585]

Ignites spontaneously on exposure to air. Reacts violently with water, oxidizing agents, halogenated hydrocarbons, alcohols, and other oxygen-containing compounds.1... [Pg.228]

Oxidizing agents Halogens Oxidize thiol groups to disulphides, sulphox-ides or disulphoxides... [Pg.139]

Dimethylacetamide is incompatible with carbon tetrachloride, oxidizing agents, halogenated compounds, and iron. It attacks plastic and rubber. Contact with strong oxidizers may cause fire. [Pg.253]

The reactivity of the halogens decreases m the order F2 > CI2 > Br2 > I2 Fluo rme is an extremely aggressive oxidizing agent and its reaction with alkanes is strongly exothermic and difficult to control Direct fluonnation of alkanes requires special equip ment and techniques is not a reaction of general applicability and will not be discussed further... [Pg.166]

The high fluorine content contributes to resistance to attack by essentially all chemicals and oxidizing agents however, PCTFE does swell slightly ia halogenated compounds, ethers, esters, and selected aromatic solvents. Specific solvents should be tested. PCTFE has the lowest water-vapor transmission rate of any plastic (14,15), is impermeable to gases (see also Barrierpolymers), and does not carbonize or support combustion. [Pg.393]

An unshared electron pair on phosphoms reacts with oxidizing agents, eg, hydrogen peroxide, sulfur, or halogens. [Pg.358]

Halogen Displacement. Poly(phenylene oxide)s can also be prepared from 4-halo-2,6-disubstituted phenols by displacement of the halogen to form the ether linkage (48). A trace of an oxidizing agent or free radical initiates the displacement reaction. With 4-bromo-2,6-dimethylphenol, the reaction can be represented as in equation 10 ... [Pg.329]

Halogen-substituted succinimides are a class of products with important appHcations. /V-Bromosuccinimide [128-08-5] mp 176—177°C, is the most important product ia this group, and is prepared by addition of bromine to a cold aqueous solution of succinimide (110,111) or by reaction of succinimide with NaBr02 iu the presence of HBr (112). It is used as a bromination and oxidation agent ia the synthesis of cortisone and other hormones. By its use it is possible to obtain selective bromine substitution at methylene groups adjacent to double bonds without addition reactions to the double bond (113). [Pg.536]

Generally these derivatives are rather unstable and behave as oxidizing and halogenating agents. 1-Iodoimidazoles are more stable than other analogs. [Pg.110]

Oxaziridines are powerful oxidizing agents. Free halogen is formed from hydrobromic acid (B-67MI50800). Reduction by iodide in acidic media generally yields a carbonyl compound, an amine and two equivalents of iodine from an oxaziridine (1). With 2-alkyl-, 2-acyl and with N-unsubstituted oxaziridines the reaction proceeds practically quantitatively and has been used in characterization. Owing to fast competing reactions, iodide reduction of 2-aryloxaziridines does not proceed quantitatively but may serve as a hint to their presence. [Pg.208]

Chlorine is a member of the halogen (salt-forming) group of elements and is derived from chlorides by the action of oxidizing agents and, most frequently, by electrolysis. As a gas, it combines directly with nearly all elements. At 10 C, 1 volume of water dissolves about 3.10 volumes of chlorine at 30 C, only 1.77 volumes of CI2 are dissolved in 1 volume of water. [Pg.464]


See other pages where Oxidizing agent halogens is mentioned: [Pg.556]    [Pg.205]    [Pg.53]    [Pg.217]    [Pg.950]    [Pg.293]    [Pg.950]    [Pg.242]    [Pg.420]    [Pg.126]    [Pg.1595]    [Pg.556]    [Pg.205]    [Pg.53]    [Pg.217]    [Pg.950]    [Pg.293]    [Pg.950]    [Pg.242]    [Pg.420]    [Pg.126]    [Pg.1595]    [Pg.98]    [Pg.409]    [Pg.41]    [Pg.204]    [Pg.426]    [Pg.272]    [Pg.207]    [Pg.367]    [Pg.454]    [Pg.72]    [Pg.426]    [Pg.432]    [Pg.32]    [Pg.47]    [Pg.135]    [Pg.166]    [Pg.581]    [Pg.674]    [Pg.2315]    [Pg.292]    [Pg.72]   
See also in sourсe #XX -- [ Pg.215 , Pg.216 , Pg.533 , Pg.556 ]

See also in sourсe #XX -- [ Pg.246 , Pg.247 , Pg.592 , Pg.617 ]




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1-oxide halogenation

Halogen oxidants

Halogenating agents

Halogenating agents oxidations

Halogenating agents oxidations

Halogenation oxidation

Halogens oxides

Halogens oxidizers

Oxidation agent

Oxidation halogens

Oxidation oxidizing agent

Oxidative halogenation

Oxidizing agents

Oxidizing agents oxidants

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