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Phenols, Properties Unsaturated

Separations based upon differences in the chemical properties of the components. Thus a mixture of toluene and anihne may be separated by extraction with dilute hydrochloric acid the aniline passes into the aqueous layer in the form of the salt, anihne hydrochloride, and may be recovered by neutralisation. Similarly, a mixture of phenol and toluene may be separated by treatment with dilute sodium hydroxide. The above examples are, of comse, simple apphcations of the fact that the various components fah into different solubihty groups (compare Section XI,5). Another example is the separation of a mixture of di-n-butyl ether and chlorobenzene concentrated sulphuric acid dissolves only the w-butyl other and it may be recovered from solution by dilution with water. With some classes of compounds, e.g., unsaturated compounds, concentrated sulphuric acid leads to polymerisation, sulphona-tion, etc., so that the original component cannot be recovered unchanged this solvent, therefore, possesses hmited apphcation. Phenols may be separated from acids (for example, o-cresol from benzoic acid) by a dilute solution of sodium bicarbonate the weakly acidic phenols (and also enols) are not converted into salts by this reagent and may be removed by ether extraction or by other means the acids pass into solution as the sodium salts and may be recovered after acidification. Aldehydes, e.g., benzaldehyde, may be separated from liquid hydrocarbons and other neutral, water-insoluble hquid compounds by shaking with a solution of sodium bisulphite the aldehyde forms a sohd bisulphite compound, which may be filtered off and decomposed with dilute acid or with sodium bicarbonate solution in order to recover the aldehyde. [Pg.1091]

Heteroatom functionalized terpene resins are also utilized in hot melt adhesive and ink appHcations. Diels-Alder reaction of terpenic dienes or trienes with acrylates, methacrylates, or other a, P-unsaturated esters of polyhydric alcohols has been shown to yield resins with superior pressure sensitive adhesive properties relative to petroleum and unmodified polyterpene resins (107). Limonene—phenol resins, produced by the BF etherate-catalyzed condensation of 1.4—2.0 moles of limonene with 1.0 mole of phenol have been shown to impart improved tack, elongation, and tensile strength to ethylene—vinyl acetate and ethylene—methyl acrylate-based hot melt adhesive systems (108). Terpene polyol ethers have been shown to be particularly effective tackifiers in pressure sensitive adhesive appHcations (109). [Pg.357]

Previous studies in conventional reactor setups at Philip Morris USA have demonstrated the significant effectiveness of nanoparticle iron oxide on the oxidation of carbon monoxide when compared to the conventional, micron-sized iron oxide, " as well as its effect on the combustion and pyrolysis of biomass and biomass model compounds.These effects are derived from a higher reactivity of nanoparticles that are attributed to a higher BET surface area as well as the coordination of unsaturated sites on the surfaces. The chemical and electronic properties of nanoparticle iron oxide could also contribute to its higher reactivity. In this work, we present the possibility of using nanoparticle iron oxide as a catalyst for the decomposition of phenolic compounds. [Pg.222]

Very recently, attempts have been made to develop PP/EOC TP Vs. In order to make TPVs based on PP/EOC blend systems, phenolic resin is ineffective because the latter needs the presence of a double bond to form a crosslinked network structure. Peroxides can crosslink both saturated and unsaturated polymers without any reversion characteristics. The formation of strong C-C bonds provides substantial heat resistance and good compression set properties without any discoloration. However, the activity of peroxide depends on the type of polymer and the presence of other ingredients in the system. It has been well established that PP exhibits a (3-chain scission reaction (degradation) with the addition of peroxide. Hence, the use of peroxide only is limited to the preparation of PP-based TPVs. Lai et al. [45] and Li et al. [46] studied the fracture and failure mechanism of a PP-metallocene based EOC based TPV prepared by a peroxide crosslinking system. Rajesh et al. [Pg.229]

As hydroxyl substitution products possessing both acid and alcohol properties the phenols yield salts, esters and ethers. The salts and esters have been sufficiently considered. The ethers of phenols, especially of those which contain an unsaturated side chain, include several important compounds. [Pg.621]

The materials employed for making hollow microspheres include inorganic materials such as glass and silica, and polymeric materials such as epoxy resin, unsaturated polyester resin, silicone resin, phenolics, polyvinyl alcohol, polyvinyl chloride, polyjM-opylene and polystyrene, among others, commercial jx oducts available are glass, silica, phenolics, epoxy resin, silicones, etc. Table 36 shows low-density hollow spheres. Table 37 shows physical properties of glass microspheres, and Table 38 shows comparison of some fillers on the physical properties of resulting foams (10). [Pg.148]

Polymerization reactions involve the union of a number of similar molecules to form a single complex molecule. A polymer is any compound, each molecule of which is formed out of a number of molecules which are all alike, and which are called monomers. In many cases polsonerization can be reversed and the poisoner be resolved to the monomer. Many polymerization reactions which are of industrial importance involve in the initial stages condensations, that is, reactions in which elimination of water or other simple molecules takes place. Compounds which polymerize have some type of unsaturation in the molecule. Olefins, unsaturated halides, esters, aldehydes, dicarboxylic acids, anhydrides, amino acids and amides are among the important groups of compounds which are used in industrial polymerization reactions. The commercial products produced by polymerization reactions may be conveniently classified into (a) resinotds, or synthetic resins (b) elastomers, which possess rubber-like properties and (c) fibroids, used as textile fibers. Two types of resinoids are illustrated in this experiment Bakelite, formed from phenol and formaldehyde, and methacrylate resin formed from an unsaturated ester. [Pg.343]

Alcohols and phenols contain the hydroxyl group (—O—H) as their functional group. Alcohols may be considered to be derived from saturated or unsaturated hydrocarbons by the replacement of at least one H atom by a hydroxyl group. The properties of alcohols result from a hydroxyl group attached to an aliphatic carbon atom, —C—O—H. Ethanol (ethyl alcohol) is the most common example (Figure 27-14). [Pg.1066]

The polymer eomponent, whieh is a thermosetting resin, forms eross-linked bonds between chains of molecules, whieh enhanees the eharacteristic of the produet. Unsaturated polyesters and vinyl esters are primarily used as resin systems. Epoxies are also used in some eases, but the eure eyele is longer. Phenolic resins have gained importanee these days because of their inherent properties, especially in applications that require lower flammability, reduced smoke generation, and higher thermal stability. New resin systems such as... [Pg.283]

Since the introduction of the first commercial thermoset, Bakelite, based on phenol formaldehyde condensation, a wide range of thermoset materials have been introduced. These are typically designed for specific properties related to their chemistry and processability. Some commercially important thermosets include phenolics, ureas, melamines, epoxy resins, unsaturated polyesters, silicones, rubbers, polyurethanes, acrylics, cyanates, polyimides, and benzocyclobutenes. ... [Pg.3031]


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See also in sourсe #XX -- [ Pg.622 ]




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Phenols, properties

Unsaturated phenols

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