Chlorine description

Although every redox titrimetric method has its own unique considerations, the following description of the determination of total residual chlorine in water provides an instructive example of a typical procedure. 

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 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 distinctive odor of trichloroethylene may not necessarily provide adequate warning of exposure, because it quickly desensitizes olfactory responses. EataUties have occurred when unprotected workers have entered unventilated areas with high vapor concentrations of trichloroethylene or other chlorinated solvents. Eor a complete description of proper entry to vessels containing any chlorinated solvent, see ASTM D4276-84, Standard Practice for Confined Area Entry (34). 

The solid disulfide reacts explosively with chlorine or bromine. At low temperatures in certain non-aqueous solvents, e.g. chloroform, CISCSN3 and BrSCSN3 are probably formed, but the extreme instability of these compounds has precluded their exact analysis and description. However, the reaction between cyanogen bromide and the potassium salt of the thiol yields the well-defined cyanide NCSCSN3,... 

The remaining four elements form molecular solids. The atoms of white phosphorus, sulfur, and chlorine are strongly bonded into small molecules (formulas, P4, S8, and Cl2, respectively) but only weak attractions exist between the molecules. The properties are all appropriate to this description. Of course there is no simple trend in the properties since the molecular units are so different. 

Some formulas, such as the formula for table salt, are very simple. You don t need a picture, just a description of the two elements that make it up sodium and chlorine. The formula is ... 

The synthesis gas is mainly used for the production of methanol (70%). Another part (20%) is used for electricity production. Waste gas products are incinerated the fate of any chlorine is not clear from the various descriptions available. Inorganic materials are converted into a slag, with low leaching characteristics (landfill class 1 according to the German TA Siedlungsabfall). 

From the description above it already can be deduced that this plant can deal with a lot of waste types and hence is rather robust in terms of acceptance criteria. S VZ has experience with treating mixed plastics waste, waste derived fuel (a mixture of plastics, wood and paper), the shredder light fraction of car wrecks, and the plastic fraction from shredded white goods and electronics. SVZ can handle on average 2% chlorine in MPW, with short-term excursions to 6%. The overall chlorine content has to be controlled by a right blend with other waste types. SVZ does not favour a high... 

The chlorination of methyl chloroformate in sunlight was first reported by Hentschel, but without a detailed description of either the procedure or the results. The first step of the present procedure for the preparation of trichloromethyl chloroformate utilizes an ultraviolet light source and affords a simple and reproducible way to obtain this reagent. Although trichloromethyl chloroformate may also be synthesized by photochemical chlorination of methyl formate,the volatility of methyl formate causes losses during the reaction and increases the hazard of forming an explosive mixture of its vapor and chlorine gas. The preparation of trichloromethyl chloroformate by chlorination of methyl chloroformate in the dark with diacetyl peroxide as initiator has been reported. However, the procedure consists of several steps, and the overall yield is rather low. 

Clearly, it would be inadequate to refer to this compound as you know, that thing with five carbons and an OH coming off the side with a chlorine on a double bond. First of all, there are too many other compounds that fit that fuzzy description. And even if we could come up with a very adequate description that could only be this one compound, it would take way too long (probably an entire paragraph) to describe. By following the rules of nomenclature, we can unambiguously describe this molecule with just a few letters and numbers Z-2-chloropent-2-en-l-ol. 

Such a reaction would occur if we exposed a metal surface to either oxygen or chlorine. A MX film would build up on the metal surface and growth of a film would occur by diffusion. In the initial description, we ignored vacancy and interstltleil diffusion and presented only the charged particles, M + and 0= as the diffusing species (see section 4.5.). In actuality, the metal diffuses as the interstitial, Mi2+, and the anion as Oi=. ... 

The precise structural role played by the water molecules in these cements is not clear. In the zinc oxychloride cement, water is known to be thermally labile. The 1 1 2 phase will lose half of its constituent water at about 230 °C, and the 4 1 5 phase will lose water at approximately 160 C to yield a mixture of zinc oxide and the 1 1 2 phase. Water clearly occurs in these cements as discrete molecules, which presumably coordinate to the metal ions in the cements in the way described previously. However, the possible complexities of structure for these systems, which may include chlorine atoms in bridging positions between pairs of metal atoms, make it impossible to suggest with any degree of confidence which chemical species or what structural units are likely to be present in such cements. One is left with the rather inadequate chemical descriptions of the phases used in even the relatively recent original literature on these materials, from which no clear information on the role of water can be deduced. 

In the results the emissions of mercury appear to have a very substantial contribution for the human toxicity impact score. These emissions are caused by the coproduction of chlorine and sodium hydroxide by electrolysis using a mercury cell. However, this technique is phased out. Therefore, the process descriptions in the Ecoinvent database do not represent up to date technology. In the Ecoinvent database the process for PVC production, in which chlorine is used as one of the compounds, is an aggregated processes based on, seemingly outdated, data from PlasticsEurope. These outdated data also influence the impacts related to waste treatment by incineration because sodium hydroxide is necessary for the waste incineration process. 

In this section we give a simple and qualitative description of chemisorption in terms of molecular orbital theory. It should provide a feeling for why some atoms such as potassium or chlorine acquire positive or negative charge upon adsorption, while other atoms remain more or less neutral. We explain qualitatively why a molecule adsorbs associatively or dissociatively, and we discuss the role of the work function in dissociation. The text is meant to provide some elementary background for the chapters on photoemission, thermal desorption and vibrational spectroscopy. We avoid theoretical formulae and refer for thorough treatments of chemisorption to the literature [2,6-8],... 

The description of ISAT presented above follows closely the presentation in Pope (1997), and has been employed successfully in transported PDF studies of combusting systems (Saxena and Pope 1998 Saxena and Pope 1999 Xu and Pope 2000) and vapor-phase chlorination (Shah and Fox 1999 Raman et al. 2001 Raman et al. 2003). A commercial version of ISAT is described in Masri et al. (2003) and has the following additional features ... 

Yin, G. Ni, Y., (1998) Quantitative description of the chloride effect on chlorine dioxide generation from the C102-H0C1 reaction. Canadian Journal of Chemical Engineering, 76, 921-926. 

Note. For a full description of the toxicology of this compound, see the entry for chlorodiphenyl, 42% chlorine immediately preceding this entry. Special characteristics of the 54% chlorine compound are given below. 

While the situation with respect to simple vinyl polymers is straightforward, the tacticity and geometrical arguments are more complicated for more complex polymers. Here we will only briefly consider this situation. Before we move to an illustration of this let us view two related chloride-containing materials pictured below. We notice that by inserting a methylene between the two chlorine-containing carbons the description of the structure changes from racemic to meso. Thus, there exists difficulty between the historical connection of meso with isotactic and racemic with syndiotactic. 

The primary purpose of this chapter is to provide public health officials, physicians, toxicologists, and other interested individuals and groups with an overall perspective on the toxicology of chlorine dioxide and chlorite. It contains descriptions and evaluations of toxicological studies and epidemiological investigations and provides conclusions, where possible, on the relevance of toxicity and toxicokinetic data to public health. 

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