Hydrocarbons, hydrocarbon ethers

Benzene 80.1 2.28b 3 3 Aromatics, hydrocarbons, hydrocarbons Ether, ethyl acetate, to remove from crystals Suspected... 

Solubility soluble in chlorinated hydrocarbons, hydrocarbons, ethers, alcohols, pyridine, and other commonly used organic solvents insoluble in water. 

Almost insoluble in cold water. Higher alcohols (including benzyl alcohol), higher phenols (e.g., naphthols), metaformaldehyde, paraldehyde, aromatic aldehydes, higher ketones (including acetophenone), aromatic acids, most esters, ethers, oxamide and domatic amides, sulphonamides, aromatic imides, aromatic nitriles, aromatic acid anhydrides, aromatic acid chlorides, sulphonyl chlorides, starch, aromatic amines, anilides, tyrosine, cystine, nitrocompounds, uric acid, halogeno-hydrocarbons, hydrocarbons. 

Acid anhydrides Carbohydrates Quinones Hydrocarbons Ethers... 

Saturated and aromatic hydrocarbons Ethers Anhydrous calcium chloride anhydrous calcium sulphate metallic sodium phosphorus pentoxide. 

CaH/ Hydrocarbons, ethers, amines, esters, higher alcohols 1 X 10-5 0.85 Impossible... 

Na-Pb alloy Hydrocarbons, ethers (Eor solvents only) 0.08 Impossible... 

Typical nonsieve, polar adsorbents are siUca gel and activated alumina. Kquilihrium data have been pubUshed on many systems (11—16,46,47). The order of affinity for various chemical species is saturated hydrocarbons < aromatic hydrocarbons = halogenated hydrocarbons < ethers = esters = ketones < amines = alcohols < carboxylic acids. In general, the selectivities are parallel to those obtained by the use of selective polar solvents in hydrocarbon systems, even the magnitudes are similar. Consequendy, the commercial use of these adsorbents must compete with solvent-extraction techniques. 

Hydrocarbon crown ethers coordinate cations however, both the perfluoro crown ethers and the perfluorocryptands coordinate anions. For example, perfluoro crown ethers and perfluorocryptands tenaciously encapsulate O and F (60,61). 

Ma.nufa.cture. The preparation of sulfuryl chloride is carried out by feeding dry sulfur dioxide and chlorine into a water-cooled glass-lined steel vessel containing a catalyst, eg, activated charcoal. Alternatively, chlorine is passed into Hquefted sulfur dioxide at ca 0°C in the presence of a dissolved catalyst, eg, camphor, a terpene hydrocarbon, an ether, or an ester. The sulfuryl chloride is purified by distillation the commercial product is typically 99 wt % pure, as measured by ASTM distillation method D850. 

Table 2. Properties of Selected Monoterpene Hydrocarbons and Ethers...

Poly(vinyhdene chloride) also dissolves readily in certain solvent mixtures (82). One component must be a sulfoxide or A/,Al-diaIk5lamide. Effective cosolvents are less polar and have cycHc stmctures. They include aUphatic and aromatic hydrocarbons, ethers, sulfides, and ketones. Acidic or hydrogen-bonding solvents have an opposite effect, rendering the polar aprotic component less effective. Both hydrocarbons and strong hydrogen-bonding solvents are nonsolvents for PVDC. 

Solubility. One of PVP s more outstanding attributes is its solubility in both water and a variety of organic solvents. PVP is soluble in alcohols, acids, ethyl lactate, chlorinated hydrocarbons, amines, glycols, lactams, and nitroparaffins. SolubiUty means a minimum of 10 wt % PVP dissolves at room temperature (moisture content of PVP can influence solubiUty). PVP is insoluble in hydrocarbons, ethers, ethyl acetate, j -butyl-4-acetate, 2-butanone, acetone, cyclohexanone, and chlorobenzene. Both solvent polarity and H-bonding strongly influence solubiUty (77). 

Esters are most commonly prepared by the reaction of a carboxyHc acid and an alcohol with the elimination of water. Esters are also formed by a number of other reactions utilizing acid anhydrides, acid chlorides, amides, nitriles, unsaturated hydrocarbons, ethers, aldehydes, ketones, alcohols, and esters (via ester interchange). Detailed reviews of esterification are given in References 1—9. 

The thermoset polyimides are a family of heat-resistant polymers with acceptable properties up to 260°C (500°F). They are unaffected by dilute acids, aromatic and ahphatic hydrocarbons, esters, ethers, and alcohols but are attacked by dilute alkahes and concentrated inorganic acids. 

The chemical resistance of PCTFE is good but not as good as that of PTFE. Under certain circumstances substances such as chlorosulphonic acid, molten caustic alkalis and molten alkali metal will adversely affect the material. Alcohols, acids, phenols and aliphatic hydrocarbons have little effect but certain aromatic hydrocarbons, esters, halogenated hydrocarbons and ethers may cause swelling at elevated temperatures. 

Materials of these types have T s of some 290-300°C and some grades are claimed to be stable to about 400°C. Whilst resistant to hydrocarbons, halogenated hydrocarbons, ethers and acids the polymers are soluble in such materials as dimethylformamide, N-methylpyrrolidone and pyridine. Bases can cause stress cracking. These non-crystalline polymers are tough at temperatures as low as -46°C whilst at 260°C they have the strength shown by PTFE at room temperature. The polymers also exhibit excellent electrical insulation properties. 

Can Coating Ketones, Alcohols, Aromatic Hydrocarbons, Ethers... 

These four solvents can thus be termed protogenic solvents, whilst bromine trifluoride and sulphur dioxide which do not contain hydrogen are non-protonic solvents. Non-ionising solvents include hydrocarbons, ethers, esters and higher alcohols the lower alcohols, especially methanol and ethanol, do show slight ionising properties with appropriate solutes. 

Electrochemical fluorination is an important technique for obtaining saturated perfluoroheterocycles. Incorporation of a partially fluorinated group into hydrocarbon ethers enhances their stability toward fluorination with CoF3 and this approach has been extended toward electrochemical fluorination [89MI1 90JFC(49)409]. Adduct (6) obtained by free radical... 

Solubility. No quant data is in the literature. In Ref 11, p 19 die order of decreasing soly is given as w, ketones, ales)) esters) organic acids, aliphatic nitro compds) ethers, chlorinated hydrocarbons, hydrocarbons. Within each class the solubility decreases with increasing chain length... 

---