Chlorine active

Active alkali Active chlorine Active dry yeast Active dry yeasts Active oxygen (AO)... 

Displacement of activated chlorine atoms also proceeds with certain types of organic compounds, but only in the presence of Lewis acid catalysts. Particular examples include epoxides, polyhydric alcohols, trialkylphosphites (12), and P-aminocrotonates (13). These additives are commonly used in conjunction with metallic stabilizers to provide complete, high performance, commercial stabilizer packages. 

Phosphites. Tertiary phosphites are also commonly used and are particularly effective ia most mixed metal stabilizers at a use level of 0.25—1.0 phr. They can take part ia a number of different reactions duting PVC processing they can react with HCl, displace activated chlorine atoms on the polymer, provide antioxidant functionaHty, and coordinate with the metals to alter the Lewis acidity of the chloride salts. Typical examples of phosphites are triphenyl phosphite [101 -02-0], diphenyl decyl phosphite [3287-06-7], tridecyl phosphite [2929-86-4], and polyphosphites made by reaction of PCl with polyols and capping alcohols. The phosphites are often included in commercial stabilizer packages. 

Trisodium phosphate is strongly alkaline many of its appHcations depend on this property. For example, many heavy-duty cleaning compositions contain trisodium phosphate as a primary alkalinity source. The crystalline dodecahydrate itself is marketed as a cleaning compound and paint remover. Traditionally, trisodium phosphate has been used in water softening to remove polyvalent metal ions by precipitation as insoluble phosphates. Because the hypochlorite complex of trisodium phosphate provides solutions that are strongly alkaline and contain active chlorine, it is used in disinfectant cleaners, scouring powders, and automatic dishwashing formulations. 

Halogen donors are chemicals that release active chlorine or bromine when dissolved in water. After release, the halogen reaction is similar to that of chlorine or bromide from other sources. SoHd halogen donors commonly used in cooling water systems include l-bromo-3-chloro-5,5-dimethyIhydantoin, l,3-dichloro-5,5-dimethyIhydantoin, and sodium dichloroisocyanurate. 

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. 

In solutions, the concentration of available chlorine in the form of hypochlorite or hypochlorous acid is called free-available chlorine. The available chlorine in the form of undissociated A/-chloro compounds is called combined-available chlorine. Several analytical methods can be used to distinguish between free- and combined-available chlorine (8). Bleaches that do not form hypochlorite in solution like chlorine dioxide and nonchlorine bleaches can be characterized by thek equivalent available chlorine content. This can be calculated from equation 5 by substituting the number of electrons accepted divided by two for the number of active chlorine atoms. It can also be measured by iodomettic titration. 

In many patent orHterature descriptions, a stabilized chlorine dioxide solution or component is used or described. These stabilized chlorine dioxide solutions are in actuaHty a near neutral pH solution of sodium chlorite that may contain buffer salts or additives to obtain chlorite stabiHty in the pH 6—10 range. The uv spectra of these solutions is identical to that of sodium chlorite. These pH adjusted chlorite solutions can produce the active chlorine dioxide disinfectant from a number of possible organic or inorganic chemical and microbiological reactions that react, acidify, or catalyze the chlorite ion. 

The chloroisocyanurates can be used in the bleaching of cotton, synthetics, and their blends they do, however, attack proteinaceous fibers, such as silk or wool, presumably via active chlorine reaction with the peptide (amide) linkage. However, the chloroisocyanurates can be used as shrink-proofing agents in wool finishing (131), (see Textiles Wool). The same action of chlorine upon proteins contributes to the effectiveness of chloroisocyanurates in automatic dishwashers. 

Organism Peracetic acid Active chlorine Benzalkonium chloride... 

Water Tests. In colorfastness to water, ISO 10S-E01, the test specimen is placed in contact with the chosen adjacent fabrics, immersed in water, and placed wet between glass plates and left for 4 h at 37°C. After drying, the effect on the test specimen and stain on adjacents are assessed. The test, colorfastness to seawater, ISO 10S-E02, is the same as EOl but uses 30 g/L anhydrous sodium chloride solution instead of water. To test for colorfastness to chlorinated seawater/swimming baths water, ISO 10S-E03, the specimen is immersed in sodium hypochlorite solution containing either 100, 50, or 20 mg of active chlorine per Hter at pH 7.5 for 1 h at 27°C, rinsed, dried, and assessed. 

The distribution of chlorine atoms along the polymer chain has been studied in great detail. The distribution in various functional types is shown in Table 4 (18). High density polyethylene chlorosulfonated to 35% G1 and 1% S has been found to contain only 1.7% highly active chlorines, ie, reactive to weak bases. AH of these are attributed to the chlorine in the sulfonyl chloride group and those in beta position to SO2GI. No vicinal chlorides groups were found (19). 

Photometric methods are simple and rapid for the determination of components of active chlorine. But photometric reagents not always are enough sensitive and reliable. 

Authors are designed row sensitive and selective test-systems for analysis of heavy metals, active chlorine, phenols, nitrates, nitrites, phosphate etc. for analysis of objects of an environment and for control of ions Ee contents in the technological solutions of KH PO, as well as for testing some of pharmacological psychotropic daigs alkaloids (including opiates), cannabis as well as pharmaceutical preparations of phenothiazines, barbiturates and 1,4-benzodiazepines series too. 

Hypochlorous acid is a weak chlorinating agent. In acidic solution, it is converted to a much more active chlorinating agent Although early mechanistic studies suggested that Cl" " might be formed under these conditions, it has since been shown that this is not the... 

Activated fluorine is replaced in preference to activated chlorine m the Sf,jAr reaction (equation 3). 

Elimination of a molecule of methyl chloride takes place also in several other cy-clizations of organyl methyl tellurides containing active chlorine atoms, e.g., in the synthesis of tellurocoumarin (84JHC1281) and telluroisocoumarin (80JOC3535). 

Diuretic activity can be retained in the face of replacement of one of the sulfonamide groups by a carboxylic acid or amide. Reaction of the dichlorobenzoic acid, 174, with chlorsulfonic acid gives the sulfonyl chloride, 175 this is then converted to the amide (176). Reaction of that compound with furfuryl ine leads to nucleophilic aromatic displacement of the highly activated chlorine at the 2 position. There is thus obtained the very potent diuretic furosemide (177). ... 

Nafimidone (93), an anticonvulsant compound, also contains an imidazole moiety It seems to have been discovered by accident during a search for antifungal agents Its synthesis is straightforward involving displacement with imidazole of the activated chlorine atom of chloro-methyl-p-naphthylketone (92) [32]... 

Bleich-beize, /. bleaching mordant, -chlor, n. chlorine for bleaching active chlorine. 

Chloro-5-nitrobenzamido)-5-methylphenol (5), which possesses an activated chlorine atom, cyclizes in aqueous sodium hydroxide to the dibenzoxazepinone 6.41... 

Several authors (8,9) suggested that PSCs could play a major role in the depletion of ozone over Antarctica by promoting the release of active chlorine from its reservoir species, mainly by the following reaction ... 

In these reagents chloramine T — a white powder containing approximately 25 % active chlorine - is used as a substitute for hypochlorite or chlorine gas. The reactions take place in either acid (hydrochloric acid, sulfuric acid, trichloroacetic acid) or alkaline medium (sodium hydroxide). 

Treatment with chlorine gas converts amines to chloramines, whose active chlorine oxidizes iodide to iodine. This then forms the well-known, deep blue iodine-starch complex [13]. 

Presumably the active chlorine of the chloramines formed by reaction with chlorine gas or hypochlorite reacts with TDM in the presence of acetic acid to yield dark blue, mesomerically stabilized quinoid reaction products that possibly rearrange to yield triphenylmethane dyestuffs. 

The action of chlorine gas produces, for example, chloramine derivatives from herbicides, amino acids, peptides and proteins the active chlorine of these derivatives then... 

Substances containing active chlorine or bromine oxidize iodide ions — if necessary under the influence of UV light - to iodine, which reacts with starch to yield the well-known intense blue starch-iodine inclusion complex. 

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