Polyvinyl chloride hydrocarbon ester

It is a colorless to straw-yellow, oily liquid with a peppermint-like odor. It will darken and form a solid residue an exposure arxl aging. It is miscible with most organic liquids and it is a good solvent for such substances os nitrocellulose, ethylcellulose, law-viscosity cellulose acetate, polyvinyl chloride, vinyl resins, hydrocarbons, raw linseed oil, kauri gum, rosin, ester gum and synthetic rubber. It will only partly dissolve shellac and dewaxed dammar. 

Plasticizers are most commonly liquid esters of low volatUity, which are blended into rigid thermoplastic polymers to make them soft and flexible. Most are esters of phthatic, phosphoric, and adipic acids. Major use is in polyvinyl chloride (PVC) elastoplastics. Another major use, rarely mentioned in the literature, is the addition of hydrocarbon oils to rubber to improve processability. Plasticizers are also used to improve melt processabUity and toughness of rigid plastics such as cellulose esters and ethers, and they are used in a variety of specialized apphcations. In some cases, they perform dual functions such as thermal stabilization or flame retardance. This gives the individual processor the ability to tailor properties for each produet. 

Vinyl resins (1934) n. According to common chemical nomenclature, all resins and polymers made from monomers containing the vinyl group, H2C=CHX. In the chemical literature, polystyrene, polyolefins, polymethyl methacrylate and many other styrenic, ethenic, and acrylic co-polymers are classified as vinyls. In the plastics literature, the above materials are given their own classifications and the term vinyl is restricted to compounds in which X, above, is not H, a hydrocarbon radical, nor an acrylic-type ester. In daily use, the term vinyl plastics refers primarily to polyvinyl chloride and its co-polymers, and secondarily to the following polyvinyl acetal, polyvinyl acetate, poly-vinyl alcohol, polyvinyl but-yral, poly(n-vinylcar-bazole), polyvinyl dichloride, polyvinyl formal, polyvinylidene chloride, polyisobutylvinyl ether, and poly (1-vinylpyrrolidone). Mishra MKM, Yagd Y (1998) Handbook of vinyl polymerization. Marcel Dekker, New York. 

Most plasticizers are used with polyvinyl chloride (PVC). Some go into such plastics as cellulosics, nylon, polyolefins, and styrenics. Plasticizers are typically di- and tri-esters of aromatic or aliphatic acids and anhydrides. Epoxidized oil, phosphate esters, hydrocarbon oils, and some other materials also function as plasticizers. In some cases, it is difficult to discern whether a particular polymer additive functions as a plasticizer, lubricant, or flame retardant. The most popular plasticizers are the phthalates, followed by the epoxies, adipates, azelates, trimeflitates, phosphates, polyesters, and others. There are a number of discrete chemical compounds within each of these categories. As a result, the total number of plasticizers available is substantial. 

Vinyl (PVC) - Polyvinyl Chloride has good to excellent resistance to amines and aromatics, inorganic acids, bases and salts. However, this low-cost elastomer has poor resistance to halogenated hydrocarbons, ketones and esters. 

Polymer solutions (i.e., polymers dissolved in low molecular weight solvents) are widely used in industrial compoimds of varying complexity. Synthetic hydrocarbon elastomers are often marketed as oil-extended rubber , which are solutions of the basic elastomer with hydrocarbon mineral oils. Polyvinyl chloride is often marketed in a plasticized form, which are solutions involving low molecular weight esters. Many additives dissolve in polymers forming polymer solutions. In this chapter, we consider the fundamental thermodynamics and rheology of polymer solutions as well as important applications. 

A significant number of works are concerned with the development of new membranes for the separation of mixtures of aromatic/alicyclic hydrocarbons [10,11,77-109]. For example, the following works can be mentioned. A mixture of cellulose ester and polyphosphonate ester (50 wt%) was used for benzene/cyclohexane separation [113]. High values of the separation factor and flux were achieved (up to 2 kg/m h). In order to achieve better fluxes and separation factors the attention was shifted to the modification of polymers by grafting technique. Grafted membranes were made of polyvinylidene fluoride with 4-vinyl pyridine or acrylic acid by irradiation [83]. 2-Hydroxy-3-(diethyl-amino) propyl methacrylate-styrene copolymer membranes with cyanuric chloride were prepared, which exhibited a superior separation factor /3p= 190 for a feed aromatic component concentration of 20 wt%. Graft copolymer membranes based on 2-hydroxyethyl methylacrylate-methylacrylate with thickness 10 pm were prepared [85]. The membranes yielded a flux of 0.7 kg/m h (for feed with 50 wt% of benzene) and excellent selectivity. Benzene concentration in permeate was about 100 wt%. A membrane based on polyvinyl alcohol and polyallyl amine was prepared [87]. For a feed containing 10 wt% of benzene the blend membrane yielded a flux of 1-3 kg/m h and a separation factor of 62. 

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