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In the laboratory it is occasionally used as a source of chlorine, with elimination of ethene and chloride. Via several steps, 1,2-dichloroethane is a precursor to 1,1,1-trichloroethane . Historically, before leaded petrol was phased out, chloroethanes were used as an additive in petrol to prevent lead buildup in engines.
This page contains tables of azeotrope data for various binary and ternary mixtures of solvents. The data include the composition of a mixture by weight (in binary azeotropes, when only one fraction is given, it is the fraction of the second component), the boiling point (b.p.) of a component, the boiling point of a mixture, and the specific gravity of the mixture.
Chloroethane is produced by hydrochlorination of ethylene: [11]. C 2 H 4 + HCl → C 2 H 5 Cl. At various times in the past, chloroethane has also been produced from ethanol and hydrochloric acid, from ethane and chlorine, or from ethanol and phosphorus trichloride, but these routes are no longer economical.
Depending on the effluent nature, an increase of the conductivity of the solution may be required: the value of 1000 mS/cm is commonly taken as a threshold. [13] Salts like sodium chloride or sodium sulfate can be added to the solution, acting as electrolytes, thus raising the conductivity. Typical values of salts concentration are in the range ...
A dealkalizer contains strong base anion exchange resin that exchanges chloride (the Cl – ion of the NaCl) for carbonate (CO − 3), bicarbonate (H C O − 3) and sulfate (SO 2− 4). As water passes through the anion resin the carbonate, bicarbonate and sulfate ions are exchanged for chloride ions.
The solution travels to a tank that separates the hydrogen gas based on its low density. [1] Only water and sodium chloride are used. The simplified chemical reaction is: NaCl + H 2 O + energy → NaOCl + H 2 [citation needed] That is, energy is added to sodium chloride (table salt) in water, producing sodium hypochlorite and hydrogen gas.