Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

INDEX Chlorine

Classification and Labeling. According to Directive EEC 67/548, Annex I, chlorine (Index no. 017-001-00-7) is classified as toxic and dangerous to the environment. The R and S phrases are ... [Pg.150]

Dichloroacetic acid [79-43-6] (CI2CHCOOH), mol wt 128.94, C2H2CI2O2, is a reactive intermediate in organic synthesis. Physical properties are mp 13.9°C, bp 194°C, density 1.5634 g/mL, and refractive index 1.4658, both at 20°C. The Hquid is totally miscible in water, ethyl alcohol, and ether. Dichloroacetic acid K = 5.14 X 10 ) is a stronger acid than chloroacetic acid. Most chemical reactions are similar to those of chloroacetic acid, although both chlorine... [Pg.88]

Table 11. Effect of Chlorine and Antimony Oxide on the Oxygen Index of Unsaturated Polyesters... Table 11. Effect of Chlorine and Antimony Oxide on the Oxygen Index of Unsaturated Polyesters...
Chlorine. Nearly all chlorine compounds are readily soluble in water. As a result, the major reservoir for this element in Figure 1 is the ocean (5). Chloride, as noted earHer, is naturally present at low levels in rain and snow, especially over and near the oceans. Widespread increases in chloride concentration in mnoff in much of the United States can be attributed to the extensive use of sodium chloride and calcium chloride for deicing of streets and highways. Ref. 19 points out the importance of the increased use of deicing salt as a cause of increased chloride concentrations in streams of the northeastern United States and the role of this factor in the chloride trends in Lake Ontario. Increases in chloride concentration also can occur as a result of disposal of sewage, oil field brines, and various kinds of industrial waste. Thus, chloride concentration trends also can be considered as an index of the alternation of streamwater chemistry by human development in the industrialized sections of the world. Although chlorine is an essential element for animal nutrition, it is of less importance for other life forms. [Pg.201]

Water Quality Maintenance. In addition to controlling algae and microorganisms such as bacteria, proper swimming pool maintenance requires control of free and combined available chlorine, pH, alkalinity, hardness, and saturation index. Ranges for various swimming pool parameters (Table 2) are recommended by The National Spa and Pool Institute (14). [Pg.297]

Paraffin carbon chain length Nominal chlorine contents, %w / w Color hazen (APHA) Viscosity, mPa-s (=cP) Density, g/mL Thermal stability, %w/wHCl Volatihty, %w/w Refractive index... [Pg.42]

The light chlorophenols, normally have a purity greater than 98.5%, but they often reach over 99%, or even 99.5% with direct phenol chlorination. The APHA color test is always below 100. For 2,4,6-ttichlorophenol, the 2,4,5-trichlorophenol content constitutes an essential quaUty index and should be under 20 mg/kg. None of the light chlorophenols contain any polychlorodibenzoparadioxins or polychlorodibenzofurans. [Pg.80]

Additives for lubricating oils providing a combination of viscosity index improvement (VII) and dispersancy have also been reported. These additives are prepared from ethyleneamines by reaction with various Vll-type polymers that have been chlorinated or modified in some other way to provide an ethyleneamine reaction site. Antimst additives for lubricating oils have been prepared by reaction of polyamines with fatty acids followed by reaction with polyalkylenesuccinic anhydrides (178,179). [Pg.47]

Solvent — The transition energy responsible for the main absorption band is dependent on the refractive index of the solvent, the transition energy being lower as the refractive index of the solvent increases. In other words, the values are similar in petroleum ether, hexane, and diethyl ether and much higher in benzene, toluene, and chlorinated solvents. Therefore, for comparison of the UV-Vis spectrum features, the same solvent should be used to obtain all carotenoid data. In addition, because of this solvent effect, special care should be taken when information about a chromophore is taken from a UV-Vis spectrum measured online by a PDA detector during HPLC analysis. [Pg.467]

As 1,2,5-thiadiazole analogues, potent HlV-1 reverse transcriptase inhibitors, some simple 1,2,5-oxadiazoles, compounds 4-6 (Fig. 9), have been synthesized using the traditional Wieland procedure as key for the heterocycle formation [121]. Such as thiadiazole parent compounds, derivative with chlorine atoms on the phenyl ring, i.e., 5, showed the best anti-viral activity. Selectivity index (ratio of cytotoxic concentration to effective concentration) ranked in the order of 5 > 6 > 4. The activity of Fz derivative 6 proved the N-oxide lack of relevance in the studied bioactivity. These products have been claimed in an invention patent [122]. On the other hand, compound 7 (Fig. 9) was evaluated for its nitric oxide (NO)-releasing property (see below) as modulator of the catalytic activity of HlV-1 reverse transcriptase. It was found that NO inhibited dose-dependently the enzyme activity, which is hkely due to oxidation of Cys residues [123]. [Pg.279]

The SEC mechanism demands only an isocratic (constant composition) solvent system with normally a single solvent. The most frequently used organic solvents are THF, chloroform, toluene, esters, ketones, DMF, etc. The key solvent parameters of interest in SEC are (i) solubility parameter (ii) refractive index (iii) UV/IR absorbance (iv) viscosity and (v) boiling point. Sample solutions are typically prepared at concentrations in the region of 0.5-5 mg mL-1. In general an injection volume of 25-100p,L per 300 x 7.5 mm column should be employed. For SEC operation with polyolefins chlorinated solvents (for detector sensitivity and increased boiling point) and elevated temperatures (110 to 150 °C) are required to dissolve olefin polymer. HFIP is the preferred solvent for SEC analysis of polyesters and polyamides. [Pg.259]

We have recently evaluated the chlorendic imide/hindered phenol for its effect on the oxygen index of polyethylene, and we found only a miniscule increase, not considred statistically significant, in comparison to the same loading of chlorine as chlorendic anhydride. We believe that if the antioxidant approach to flame retardancy is to be successful, special high temperature antioxidant structures must be designed for this purpose. [Pg.102]

Some synonyms in the Alphabetical index are followed by bracketed notations. These notations provide additional clarifying information about the entry such as composition, modifications to the agents (e.g., thickened, dusty, binary), or a note for historical context. For example, "White Star" was a gas blend that was employed by the British in World War I consisting of 50% phosgene and 50% chlorine. The entry appears as ... [Pg.617]

The second structural property described by the 4ypc index is the substitution pattern on the benzene ring. The value of the 4ypc index increases sharply with the degree of substitution, while in the isomeric classes of substituted benzenes it increases with the proximity of substituents. Thus, this structural parameter has also been found to be very useful in describing activities and properties of polysubstituted benzenes [103], chlorinated benzenes [279], and polychlorinated biphenyls [286]. [Pg.263]


See other pages where INDEX Chlorine is mentioned: [Pg.455]    [Pg.455]    [Pg.723]    [Pg.461]    [Pg.306]    [Pg.500]    [Pg.509]    [Pg.300]    [Pg.42]    [Pg.43]    [Pg.272]    [Pg.491]    [Pg.2037]    [Pg.2305]    [Pg.261]    [Pg.210]    [Pg.798]    [Pg.70]    [Pg.164]    [Pg.170]    [Pg.201]    [Pg.277]    [Pg.445]    [Pg.183]    [Pg.141]    [Pg.334]    [Pg.251]    [Pg.283]    [Pg.318]    [Pg.151]    [Pg.109]    [Pg.30]    [Pg.37]    [Pg.202]    [Pg.442]    [Pg.220]   
See also in sourсe #XX -- [ Pg.375 ]

See also in sourсe #XX -- [ Pg.375 ]

See also in sourсe #XX -- [ Pg.375 ]




SEARCH



Chlorinated benzenes INDEX

Chlorinated hydrocarbons 14 INDEX

INDEX chlorine compounds

© 2024 chempedia.info