Polyvinyl hydrocarbons

Polyvinyl chloride Polyvinyl chloride (PVC) and chlorinated polyvinyl chloride (CPVC) pipe and tubing are available in sizes 12 in and smaller for PVC and 4 in and smaller for CPVC. They have excellent resistance at room temperature to salts, ammonium hydroxide, and sulfuric, nitric, acetic, and hydrochloric acid but may be damaged by ketones, aromatics, and some chlorinated hydrocarbons. 

Unplasticized polyvinyl chlorides (type I) have excellent resistance to oxidizing acids other than concentrated and to most nonoxidizing acids. Resistance is good to weak and strong alkahne materials. Resistance to chlorinated hydrocarbons is not good. Polyvinyhdene chloride, known as Saran, has good resistance to chlorinated hydrocarbons. 

Polyvinyl chloride acetate copolymers Tough Very good Excellent Excellent (Aliphatic hydrocarbon, good aromatic hydrocarbon, poor) Fair, ISO F Very good Easy... 

PVC/PVA copolymer solutions Polyvinyl chloride/polyvinyl acetate copolymers can be readily dissolved in blends of aromatic hydrocarbon,... 

In a comprehensive study of trichloroethylene emission sources from industry conducted for EPA, the major source was degreasing operations, which eventually release most of the trichloroethylene used in this application to the atmosphere (EPA 1985e). Degreasing operations represented the largest source category of trichloroethylene emissions in 1983, accounting for about 91% of total trichloroethylene emissions. Other emission sources include relatively minor releases from trichloroethylene manufacture, manufacture of other chemicals (similar chlorinated hydrocarbons and polyvinyl chloride), and solvent evaporation losses from adhesives, paints, coatings, and miscellaneous uses. 

Polyvinyl benzene or styrene is the simplest Aromatic hydrocarbon which can be polymerised. Styrene was obtained by steam distillation of resin from the tree Styrax officinalis. In 1920s Staudinger gave the name styrene. Patent for polymerisation of styrene was taken out in 1911 by Matthews. 

Uses Solvent for nitrocellulose, ethyl cellulose, polyvinyl butyral, rosin, shellac, manila resin, dyes fuel for utility plants home heating oil extender preparation of methyl esters, formaldehyde, methacrylates, methylamines, dimethyl terephthalate, polyformaldehydes methyl halides, ethylene glycol in gasoline and diesel oil antifreezes octane booster in gasoline source of hydrocarbon for fuel cells extractant for animal and vegetable oils denaturant for ethanol in formaldehyde solutions to inhibit polymerization softening agent for certain plastics dehydrator for natural gas intermediate in production of methyl terLbutyl ether. 

Ahling B.. Bjorseth, A., and Lunde, G. Formation of chlorinated hydrocarbons during combustion of polyvinyl chloride. Chemosphere, 7(10) 799-806, 1978. 

Olefins or alkenes are defined as unsaturated aliphatic hydrocarbons. Ethylene and propylene are the main monomers for polyolefin foams, but dienes such as polyisoprene should also be included. The copolymers of ethylene and propylene (PP) will be included, but not polyvinyl chloride (PVC), which is usually treated as a separate polymer class. The majority of these foams have densities <100 kg m, and their microstructure consists of closed, polygonal cells with thin faces (Figure la). The review will not consider structural foam injection mouldings of PP, which have solid skins and cores of density in the range 400 to 700 kg m, and have distinct production methods and properties (456). The microstructure of these foams consists of isolated gas bubbles, often elongated by the flow of thermoplastic. However, elastomeric and microcellular foams of relative density in the range 0.3 to 0.5, which also have isolated spherical bubbles (Figure lb), will be included. The relative density of a foam is defined as the foam density divided by the polymer density. It is the inverse of the expansion ratio . 

Chlorine (from the Greek chloros for yellow-green ) is the most abundant halogen (0.19 w% of the earth s crust) and plays a key role in chemical processes. The chlor-alkali industry has been in operation since the 1890s and improvements in the technology are still important and noticeable, for example, the transition from the mercury-based technology to membrane cells [60]. Most chlorine produced today is used for the manufacture of polyvinyl chloride, chloroprene, chlorinated hydrocarbons, propylene oxide, in the pulp and paper industry, in water treatment, and in disinfection processes [61]. A summary of typical redox states of chlorine, standard potentials for acidic aqueous media, and applications is given in Scheme 2. 

Degradation of elastomers used in transfer lines and hoses by aromatic fuel components is undesirable. For this reason, elastomers used in fuel storage and distribution systems are often made of hydrocarbon-resistant elastomers such as Viton , polyvinyl chloride (PVC) and Teflon . 

As an example of thermolysis, consider the burnout of polyvinyl alcohol from a barium titanate compact in air. Initially, there is loss of hydroxyl and hydrogen side groups, leaving a conjugated hydrocarbon ... 

Original Anionic Pathway to New PA(PO)a Star-Shaped Block Polymers Based on Polyvinyl or Polydiene Hydrocarbons and Polyoxirane... 

This type of plasticization is important and several groups of polymers have been suggested for this method polymer hydrocarbons polymer halogen-containing hydrocarbons polymers containing ester groups polyvinyl ethers and acetals, and some other polymers of different constitution. 

Previous work hod shown that low temperature coke is formed from cools hooted to between 450° and 500° C. by a process of nudeation and growth of spherical bodies in the plastic vitrinite. An essentially similar process has now been found to occur with coke-oven and petroleum pitches, with polyvinyl chloride, and with some polynuclear hydrocarbons, all of which yield carbons which grophitize readily at high temperatures. The process is probably general for the initial stages of formation of such carbons from the liquid phase. Some control of the solidification process has been achieved on the laboratory scale, and the physical and chemical structure of the spherulites has been investigated. 

Recent work in this Division has shown that various substances other than vitrinites, such as pitches from coal tars and petroleum tars, polyvinyl chloride, and polynuclear hydrocarbons, develop similar mosaic structures on heating. In fact this effect occurs with most high carbon materials which pass through a plastic stage during carbonization. 

Eq. (5) in conjunction with Eqs. (8) and (9) have, so far, provided adequate representation of experimental isotherms6 32, which are characterized by an initial con vex-upward portion but tend to become linear at high pressures. Values of K, K2 and s0 have been deduced by appropriate curve-fitting procedures for a wide variety of polymer-gas systems. Among the polymers involved in recent studies of this kind, one may cite polyethylene terephthalate (PET) l2 I4), polycarbonate (PC) 19 22,27), a polyimide l6,17), polymethyl and polyethyl methacrylates (PMMA and PEMA)l8), polyacrylonitrile (PAN)15), a copolyester 26), a polysulphone 23), polyphenylene oxide (PPO)25), polystyrene (PS) 27 28), polyvinyl acetate 29) and chloride 32) (PVAc and PVC), ethyl cellulose 24) (EC) and cellulose acetate (CA) 30,3I>. A considerable number of gases have been used as penetrants, notably He, Ar, N2, C02, S02 and light hydrocarbons. 

The photodimerization of cinnamic acid and similar molecules is observed in crystals, but reactions of the same type occur in some polymers as well. Polymers such as polystyrene are made of long, saturated hydrocarbon chains with pendant groups in close contact dangling from the chain these chromophores can then interact in bimolecular photoaddition reactions. Polyvinyl car bazole and its derivatives are important examples of polymers which lead to such bimolecular interactions (e.g. exciplex formation). 

An interesting class of polyeleclrolytes, denoted by polysoaps, is obtained by attaching soap-like molecules to the polymer chain. Such a polysoap is for instance produced by the quaternization of polyvinyl-pyridine with /r-dodecyl bromide. The polysoap molecules differ from ordinary poly electrolytes in that they may reach protein-like compactness in solution. They behave like prefabricated soap micelles and solubilize hydrocarbons and other compounds insoluble in water,... 

While unaffected by water, styrofoam is dissolved by many organic solvents and is unsuitable for high-temperature applications because its heat-distortion temperature is around 77°C. Molded styrofoam objects are produced commercially from expandable polystyrene beads, but this process does not appear attractive for laboratory applications because polyurethane foams are much easier to foam in place. However, extruded polystyrene foam is available in slabs and boards which may be sawed, carved, or sanded into desired shapes and may be cemented. It is generally undesirable to join expanded polystyrene parts with cements that contain solvents which will dissolve the plastic and thus cause collapse of the cellular structure. This excludes from use a large number of cements which contain volatile aromatic hydrocarbons, ketones, or esters. Some suitable cements are room-temperature-vulcanizing silicone rubber (see below) and solvent-free epoxy cements. When a strong bond is not necessary, polyvinyl-acetate emulsion (Elmer s Glue-All) will work. 

Examples are the sulfonating of polyethylene film with chloro-sulfonic acid (60) the sulfonating of sheets of phenolformaldehyde resin (77) the treatment of a film consisting of polystyrene and polyvinylchloride with concentrated sulfuric acid (4) the sulfonating of films consisting of aliphatic vinylpolymers with chlorosulfonic acid (125) the sulfonating of copolymers of a monovinyl- and a polyvinyl compound (30). Also are used copolymers of aromatic monovinyl-compounds and linear aliphatic polyene hydrocarbons (3) copolymers of an unsaturated aromatic compound and an unsaturated aliphatic compound (76), and of reaction products of poly olefines and partially polymerized styrene (173). 

Polyvinyl chloride Dimethyl formamide, Alcohols, hydrocarbons, butyl... 

Polyvinyl acetate Aromatic hydrocarbons, ketones, chlorinated hydrocarbons, alcohols Petrol... 

Polyvinyl alcohol Formamide, water Ether, alcohols, petrol, benzene, esters, ketones, hydrocarbons... 

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