Solubility tetrachloroethane

Solubility and Solvent Resistance. The majority of polycarbonates are prepared in methylene chloride solution. Chloroform, i7j -l,2-dichloroethylene, yy -tetrachloroethane, and methylene chloride are the preferred solvents for polycarbonates. The polymer is soluble in chlorobenzene or o-dichlorobenzene when warm, but crystallization may occur at lower temperatures. Methylene chloride is most commonly used because of the high solubiUty of the polymer (350 g/L at 25°C), and because this solvent has low flammabiUty and toxicity. Nonhalogenated solvents include tetrahydrofuran, dioxane, pyridine, and cresols. Hydrocarbons (qv) and aUphatic alcohols, esters (see Esters, organic), or ketones (qv) do not dissolve polycarbonates. Acetone (qv) promotes rapid crystallization of the normally amorphous polymer, and causes catastrophic failure of stressed polycarbonate parts. 

SolubiHty of the three commercial polysulfones foUows the order PSF > PES > PPSF. At room temperature, all three of these polysulfones as weU as the vast majority of other aromatic sulfone-based polymers can be readily dissolved in a few highly polar solvents to form stable solutions. These solvents include NMP, DMAc, pyridine, and aniline. 1,1,2-Trichloroethane and 1,1,2,2-tetrachloroethane are also suitable solvents but are less desirable because of their potentially harmful health effects. PSF is also readily soluble in a host of less polar solvents by virtue of its lower solubiHty parameter. 

The process of post-chlorinating PVC was carried out during World War II in order to obtain polymers soluble in low-cost solvents and which could therefore be used for fibres and lacquers. The derivate was generally prepared by passing chlorine through a solution of PVC in tetrachloroethane at between 50°C and 100°C. Solvents for the product included methylene dichloride, butyl acetate and acetone. These materials were of limited value because of their poor colour, poor light stability, shock brittleness and comparatively low softening point. 

The solubility parameter of poly(ethylene terephthalate) is about 21.8 MPa but because it is a highly crystalline material only proton donors that are capable of interaction with the ester groups are effective. A mixture of phenol and tetrachloroethane is often used when measuring molecular weights, which are about 20 000 in the case of commercial polymers. 

Poly(alkylene terephthalate)s are soluble only in solvents such as 1,1,2,2-tetrachloroethane-phenol or o-cresol-CHCl3 mixtures, o-chlorophenol,... 

Amorphous bisphenol-A polyarylates are soluble in dioxane and in chlorinated solvents such as CH2C12, 1,2-dichlororethane, 1,1,2-trichloroethane, and 1,1,2,2-tetrachloroethane while semicrystalline and liquid crystalline wholly aromatic polyesters are only sparingly soluble in solvents such as tetrachloroethane-phenol mixtures or pentafluorophenol, which is often used for inherent viscosity determinations. 

In principle, 13C 1-NMR is a more suitable technique than H NMR for identification and characterisation of extracted flame retardants (FRs) as many FRs are partially or totally brominated. However, the solubility of many bromine-containing FRs is often insufficient for 13C NMR experiments in common solvents, such as CDCI3 and tetrachloroethane (TCE), and therefore 13C s-NMR is frequently called in. 

SOLUBILITY IN WATER Negligible. Soluble in acetone, CH3(C1), tetrachloroethane, ethylbenzoate, and ether. 

Soluble in ethanol, ether (U.S. EPA, 1985) miscible with chlorinated hydrocarbons such as chloroform, carbon tetrachloride, and tetrachloroethane. 

The ARS Technologies, Inc., Ferox process is an in situ remediation technology for the treatment of chlorinated hydrocarbons, leachable heavy metals, and other contaminants. The process involves the subsurface injection and dispersion of reactive zero-valence iron powder into the saturated or unsaturated zones of a contaminated area. ARS Technologies claims that Ferox is applicable for treating the following chemicals trichloroethene (TCE), 1,1,1-trichloroethane (TCA), carbon tetrachloride, 1,1,2,2-tetrachloroethane, lindane, aromatic azo compounds, 1,2,3-trichloropropane, tetrachloroethene (PCE), nitro aromatic compounds, 1,2-dichloroethene (DCE), vinyl chloride, 4-chlorophenol, hexachloroethane, tribromomethane, ethylene dibromide (EDB), polychlorinated biphenyls (PCBs), Freon-113, unexploded ordinances (UXO), and soluble metals (copper, nickel, lead, cadmium, arsenic, and chromium). 

Incubation of l,l,2,2,-tetrachloro[l,2- 4C]ethane with a reconstituted monooxygenase system or with intact rat liver microsomes led to the formation of a metabolite capable of binding covalently to proteins and other nucleophiles. The only soluble metabolite detected upon incubation of 1,1,2,2-tetrachloroethane with a reconstituted system was dichloroacetic acid. Pronase digestion of the C-labcllcd microsomal proteins indicated the presence of several derivatized amino acids, which were hydrolysed by alkali to yield dichloroacetic acid. The results are consistent with biotransformation of 1,1,2,2-tetrachloroethane by cytochrome P450 to dichloroacetyl chloride, which can bind covalently to various nucleophiles or hydrolyse to dichloroacetic acid (Halpert, 1982). 

All the flexible polyquinolines are readily soluble in chlorinated hydrocarbons such as methylene chloride and chloroform. Semirigid polyquinolines are soluble in tetrachloroethane or / /-cresol, but rigid polyquinolines are soluble only in strong acids like sulfuric and trifluoromethane sulfonic acid. Dilute solution properties of polyquinolines have been investigated by techniques such as membrane osmometry, light scattering, viscometry, and gel-permeation chromatography (96,97). 

There are striking differences in physical properties between the atactic and isotactic forms. The atactic material is soft, elastic, somewhat sticky, and rather soluble in solvents such as 1,1,2,2-tetrachloroethane. Isotactic polypropene is a hard, clear, strong crystalline polymer that melts at 175°. It is practically insoluble in all organic solvents at room temperature, but will dissolve to the extent of a few percent in hot 1,1,2,2-tetrachloroethane. That the difference between the atactic and isotactic polymers arises from differences in the configurations of the methyl groups on the chains is shown in a... 

Inherent viscosities of the polymers were determined at a concentration of 0.23 gram/100 ml in 60/40 phenol/tetrachloroethane at 25 °C. Polyesters for solubility determinations were prepared by conventional... 

Reported aqueous solubilities of 1,1,1,2-tetrachloroethane at various temperatures... 

FIGURE 5.1.1.10.1 Logarithm of mole fraction solubility (In x) versus reciprocal temperature for 1,1,1,2-tetrachloroethane. 

Methylation- or combined methylation-ethylation reactions were used for structure analysis of polysaccharides. The alkylation of dextran can be applied to the investigation of the branching pattern, i.e. the number and length of side chains (Sect. 2.2) [22,23]. The methylation is carried out in liquid ammonia with sodium iodide and methyl iodide, yielding products that are soluble in chloroform and tetrachloroethane [257]. 

The product from Run A was found to be completely soluble in s-tetrachloroethane at room temperature, whereas poly(chloro-p-xylyl-ene) is insoluble in this solvent at all temperatures. These marked changes in solubility characteristics are considered excellent evidence for the formation of random copolymers rather than block copolymers or mixtures of homopolymers. 

Methyltriphenylphosphonium heptahydrodiborate(l —) is a white, crystalline, air-sensitive compound. It is moderately stable at room temperature, but decomposes readily at 100°. It is soluble in methylene chloride, chloroform, and 1,1,2,2-tetrachloroethane, but insoluble in benzene, pentane, tetrahydrofuran (THF), diethyl ether, dimethyl ether, and diglyme [bis(2-methoxyethyl) ether]. 

The Span 80 with an HLB (hydrophilic-lipophilic balance number) of 4,3, which is an oil soluble liquid, was used as surfactant. The effect of the continuous medium was investigated by employing 1,1,2,2-tetrachloroethane, toluene, or decane, which have various degrees of hydrophobicity. The amounts of the components used are listed in Table 3. At room temperature (20 °C), concen-... 

The compound consists of colorless crystals which melt at 35.7°. A supercooled melt shows a refractive index = 1.5313. The compound is very sensitive toward hydrolysis. It is readily soluble in benzene, nitrobenzene, and tetrachloroethane. 

In general, starch triacetates are soluble in acetic acid and, except perhaps for potato starch triacetate, are soluble in chloroform, 1,1,2-tri-chloroethane, tetrachloroethane, and other halogenated hydrocarbons. High grade starch triacetates do not appear to be soluble in ethyl acetate or alcohol, while some controversy exists as to the extent of their solubility in pyridine and acetone. Waxy com starch triacetate, perhaps due to its smaller molecular weight, is readily soluble in a wide variety of organic solvents. 

Staudinger and Husemann determined the osmotic pressure of solutions of a potato starch acetate which had been fractionated into four parts by precipitation of its chloroform solution with ether. The molecular weights of the fractions ranged from 45,000 to 275,000. All of the fractions were soluble in chloroform, but fractions of low molecular weight were also soluble in acetone. For various concentrations of solute in either chloroform or acetone, the osmotic pressure did not increase in direct proportion to the solute concentration, but the deviation from van t Hoff s law was the smallest in the case of the acetone solutions. Osmotic pressure measurements on amylose and amylopectin tri-acetates dissolved in tetrachloroethane have been made by Meyer and co-workers, who have deduced molecular weights for these substances of approximately 78,000 and 300,000, respectively (see above discussion of the purity of these fractions). 

All of the polyformals were soluble in hot tetrachloroethane and insoluble in methanol, ethyl acetate, and naphtha. 

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