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Chlorine as oxidant

Potassium Nitrate. Potassium nitrate [7757-79-17, KNO, is produced commercially in the United States based on the reaction of potassium chloride and nitric acid (qv) (35). Ammonia (qv) oxidation is the source for the nitric acid and the reaction is manipulated chemically to yield chlorine as a co-product. The process is operated at an elevated temperature to drive the reaction to completion according to the following equation ... [Pg.534]

Pyrotechnic mixtures may also contain additional components that are added to modify the bum rate, enhance the pyrotechnic effect, or serve as a binder to maintain the homogeneity of the blended mixture and provide mechanical strength when the composition is pressed or consoHdated into a tube or other container. These additional components may also function as oxidizers or fuels in the composition, and it can be anticipated that the heat output, bum rate, and ignition sensitivity may all be affected by the addition of another component to a pyrotechnic composition. An example of an additional component is the use of a catalyst, such as iron oxide, to enhance the decomposition rate of ammonium perchlorate. Diatomaceous earth or coarse sawdust may be used to slow up the bum rate of a composition, or magnesium carbonate (an acid neutralizer) may be added to help stabilize mixtures that contain an acid-sensitive component such as potassium chlorate. Binders include such materials as dextrin (partially hydrolyzed starch), various gums, and assorted polymers such as poly(vinyl alcohol), epoxies, and polyesters. Polybutadiene mbber binders are widely used as fuels and binders in the soHd propellant industry. The production of colored flames is enhanced by the presence of chlorine atoms in the pyrotechnic flame, so chlorine donors such as poly(vinyl chloride) or chlorinated mbber are often added to color-producing compositions, where they also serve as fuels. [Pg.347]

Chlorine. Chlorine is a weU known disinfectant for water and wastewater treatment, however, it can react with organics to form toxic chlorinated compounds such as the tribalomethanes bromodichloromethane, dibromochloromethane, chloroform [67-66-3] and bromoform [75-25-2]. Chlorine dioxide [10049-04-4] may be used instead since it does not produce the troublesome chlorinated by-products as does chlorine. In addition, by-products formed by chlorine dioxide oxidation tend to be more readHy biodegradable than those of chlorine, however, chlorine dioxide is not suitable for waste streams containing cyanide. [Pg.163]

Even when their shells are closed, the animals continue to sense their environment, and as soon as the oxidant level decreases, they reopen and resume siphoning. Continuous chlorination often fails to eradicate these macrofouling creatures because of iatermptions ia the feed, which can occur for various reasons, such as chlorine tank changeover or plugging of feedlines. If the iatermption lasts long enough (1 h or possibly less), the animals have time to reoxygenate their tissues between the extended periods of chlorination. Any oxidant, such as chlorine, bromine, or ozone, eUcits the same response from these creatures. Therefore, only continuous, unintermpted appHcations are successful. [Pg.273]

The total concentration or amount of chlorine-based oxidants is often expressed as available chorine or less frequendy as active chlorine. Available chlorine is the equivalent concentration or amount of Cl needed to make the oxidant according to equations 1—4. Active chlorine is the equivalent concentration or amount of Cl atoms that can accept two electrons. This is a convention, not a description of the reaction mechanism of the oxidant. Because Cl only accepts two electrons as does HOCl and monochloramines, it only has one active Cl atom according to the definition. Thus the active chlorine is always one-half of the available chlorine. The available chlorine is usually measured by iodomettic titration (7,8). The weight of available chlorine can also be calculated by equation 5. [Pg.142]

Chlorine dioxide yields of 95% or greater have been demonstrated. The use of chlorine as an oxidant has distinct advantages because it is usually present in municipal water treatment plants for water disinfection. [Pg.486]

By similar procedures diazirines were prepared not only from simple aliphatic ketones but also from hydroxyketones and )3-aminoketones (B-67MI50800), and so were a large number of diazirines from steroidal ketones (65JA2665). Permanganate, bromine, chlorine and hypochlorite were used as oxidants. A one-step preparation of diazirines from ketones like 3-nonanone, ammonia and chlorine has been claimed in a patent (66USP3290289). 3,3-Diazirinedicarboxylic acid derivatives like (286) were obtained directly from oxime tosylates by the action of two moles of O-ethoxyamine (81AG(E)200). [Pg.233]

Chlorinated organics are hydrocarbons that have one or many chlorine atoms. Oxidation of chlorinated hydrocarbons yields COj, water vapor and hydrogen chloride (HCl) gas. Some typical chlorinated organics are TCE and PCE. These organics have calorific values as low as 5,000 BTU/lb. [Pg.479]

This last reaction is typical of many in which F3CIO can act as a Lewis base by fluoride ion donation to acceptors such as MF5 (M = P, As, Sb, Bi, V, Nb, Ta, Pt, U), M0F4O, Sip4, BF3, etc. These products are all white, stable, crystalline solids (except the canary yellow PtFe ) and contain the [F2CIO] cation (see Fig. 17.26h) which is isostructural with the isoelectronic F2SO. Chlorine trifluoride oxide can also act as a Lewis acid (fluoride ion acceptor) and is therefore to be considered as amphoteric (p. 225). For example KF, RbF and CsF yield M [F4C10] as white solids whose stabilities increase with increasing size of M+. Vibration spectroscopy establishes the C4 structure of the anion (Fig. 17.29g). [Pg.877]

Gaseous fluorine is also prepared by electrolysis of molten fluoride salts but simpler methods are available for the preparation of bromine and iodine. Chemical oxidation, usually with chlorine as the oxidizing agent, provides Br2 and I2 economically because chlorine is a relatively inexpensive chemical. The reactions are... [Pg.356]

Similiar problems of regioselectivity as in reduction reactions are encountered in oxidation reactions of porphyrins and chlorins. The oxidation of chlorins to isobacteriochlorins can be directed by insertion of zinc(II) or nickel(II) into the macrocycle. Again here, the metal-free chlorins give the bacteriochlorins whereas the metal chlorins, e.g. 1, give isobacteriochlorins, e.g. 3.15a,b I 7... [Pg.647]

Chlorination. When 75 was treated with chlorine in the presence of aluminium chloride, initial chlorination took place at the 5-position, but the reaction was rather unselective 5,8-di-, 5,7,8-tri-, and 5,6,7,8-tetra-chloroisoquinolines were also formed (64JOC329). Perchlorination has been achieved by initial reaction of the isoquinoline-aluminium chloride complex with chlorine, as above, followed by treatment with phosphorus pentachloride at 270°C in an autoclave [66JCS(C)2328]. Treatment of 1,8-dimethylisoquinoline with NCS gave the 5-chloro derivative (91NKK-1193). Meisenheimer reaction of isoquinoline 2-oxides with phosphoryl chloride gave 1-chloroisoquinoline (84MI2). [Pg.296]

The use of chlorine as an oxidizing agent for the conversion of sulphoxides into sulphones is completely unsuccessful under anhydrous conditions. In aqueous solutions, the sulphone is formed but this is usually part of a complex mixture of chlorinated sulphoxides, chlorinated sulphones and sulphonyl chlorides89, so that the reaction is usually not very useful as a preparative method for alkyl sulphones. Dimethyl sulphone has however been obtained in 70% yield in one isolated case90. In methanol solution dibenzyl sulphoxide is cleanly oxidized to dibenzyl sulphone and benzyl sulphonyl chloride in reasonable overall yield91. [Pg.979]

Chiral thietane dioxides, synthesis of 449 Chiral thiete dioxides, synthesis of 449 Chlorine compounds, as oxidizing agents... [Pg.1198]

The oxidation number of an element in a monatomic ion is the same as its charge. For example, the oxidation number of magnesium is +2 when it is present as Mg2+ ions, and the oxidation number of chlorine is — 1 when it is present as Cl" ions. The oxidation number of the elemental form of an element is 0 so magnesium metal has oxidation number 0 and chlorine in the form of Cl2 molecules also has oxidation number 0. When magnesium combines with chlorine, the oxidation numbers change as follows ... [Pg.103]


See other pages where Chlorine as oxidant is mentioned: [Pg.301]    [Pg.337]    [Pg.34]    [Pg.301]    [Pg.618]    [Pg.170]    [Pg.301]    [Pg.337]    [Pg.34]    [Pg.301]    [Pg.618]    [Pg.170]    [Pg.311]    [Pg.219]    [Pg.23]    [Pg.309]    [Pg.436]    [Pg.278]    [Pg.151]    [Pg.156]    [Pg.158]    [Pg.96]    [Pg.790]    [Pg.26]    [Pg.283]    [Pg.451]    [Pg.252]    [Pg.465]    [Pg.634]    [Pg.865]    [Pg.262]    [Pg.557]    [Pg.370]    [Pg.316]    [Pg.247]    [Pg.982]    [Pg.993]   
See also in sourсe #XX -- [ Pg.169 , Pg.184 ]




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A-chlorination

Chlorination oxidation

Chlorination oxidative

Chlorine Oxidation

Chlorine as an oxidant

Chlorine oxides

Chlorine oxidizer

Oxidants chlorine

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