Polymeric materials polyvinyl chloride

Vinyl chloride has been known for over a hundred years and its polymerization to polyvinyl chloride (PVC) was achieved in 1912. Industrial-scale production of this plastic began in 1927. PVC is still the most versatile plastic. One of the reasons for this is the numerous variations made possible by the method of manufacture of the polymer, namely by copolymerization with other monomers and their processing. Thus, PVC can be thermoformed on all conventional processing machines if the slight thermal damage is taken into consideration. Machining is easy and the material can be bonded, bent, welded, printed and thermoformed. 

The family of dialkyl peroxides includes dicumyl peroxide, which accounts for one-third of the volume of dialkyls world-wide and is the workhorse of this family of peroxides. Dicumyl peroxide is commonly used as a catalyst in polyester resin systans and for cross-linking polyethylene. Benzoyl peroxide is the most common of the diacyl peroxides. It is also used as a catalyst for curing polyester resins. Hydroperoxides are generally used as a raw material to produce other organic peroxides. The most common peroxides in this family include cumene hydroperoxide and t-butyl hydroperoxide. Ketone peroxides are mixtures of peroxides and hydroperoxides that are commonly used for room-temperature curing of polyester resins. Methyl ethyl ketone peroxide (MEKP) is the major product in this family. Peroxydicarbonates are largely used to initiate polymerization of polyvinyl chloride (PVC). 

At one time, acetylene was one of the most important organic raw materials in the chemical industry. At present, the chief use of acetylene is in the manufacture of other chemicals for polymer production, such as vinyl chloride, H2C=CHC1, which is polymerized to polyvinyl chloride (PVC). We will discuss polymers and polymerization reactions in the next chapter. 

The paper discusses the application of dynamic indentation method and apparatus for the evaluation of viscoelastic properties of polymeric materials. The three-element model of viscoelastic material has been used to calculate the rigidity and the viscosity. Using a measurements of the indentation as a function of a current velocity change on impact with the material under test, the contact force and the displacement diagrams as a function of time are plotted. Experimental results of the testing of polyvinyl chloride cable coating by dynamic indentation method and data of the static tensile test are presented. 

Quite naturally, novel techniques for manufacturing composite materials are in principal rare. The polymerization filling worked out at the Chemical Physics Institute of the USSR Academy of Sciences is an example of such techniques [49-51], The essence of the technique lies in that monomer polymerization takes place directly on the filler surface, i.e. a composite material is formed in the polymer forming stage which excludes the necessity of mixing constituents of a composite material. Practically, any material may be used as a filler the use of conducting fillers makes it possible to obtain a composite material having electrical conductance. The material thus obtained in the form of a powder can be processed by traditional methods, with polymers of many types (polyolefins, polyvinyl chloride, elastomers, etc.) used as a matrix. 

Various polymeric materials were tested statically with both gaseous and liquefied mixtures of fluorine and oxygen containing from 50 to 100% of the former. The materials which burned or reacted violently were phenol-formaldehyde resins (Bakelite) polyacrylonitrile-butadiene (Buna N) polyamides (Nylon) polychloroprene (Neoprene) polyethylene polytriflu-oropropylmethylsiloxane (LS63) polyvinyl chloride-vinyl acetate (Tygan) polyvinylidene fluoride-hexafluoropropylene (Viton) polyurethane foam. Under dynamic conditions of flow and pressure, the more resistant materials which binned were chlorinated polyethylenes, polymethyl methacrylate (Perspex) polytetraflu-oroethylene (Teflon). 

The initial halogenated polymeric materials were obtained from the polyvinyl chloride-polyvinylidene chloride, PVC-PVDC (Rovil fiber) and chlorinated polyvinyl chloride, PVC. Dehydrochlorination was performed in the presence of a base solution in a polar organic solvent (dimethylsulfoxide, acetone or tetrahydro-furane). The products were filtered and extracted with water in a Soxhlet apparatus until all chloride ions were removed. Thermal treatment was performed in a tubular furnace in CO flow at 10 cm min". ... 

Carbon materials were obtained from polymeric precursors produced by chemical dehydrochlorination of polyvinyl chloride-polyvinyUdene chloride and chlorinated polyvinyl chloride in the presence of a strong base, followed by subsequent thermal treatment under relatively mild conditions. The sorbents obtained have three types of pores ultra-micropores, miaopores, and mesopores. hi this respect, they differ substantially from microporous activated carbons such as Saran, conventionally prepared from chlorinated polymers by thermal treatment without chemical dehydrochlorination. 

Polymers containing polar groups, such as polyvinyl chloride (PVC), and condensation polymers, such as Nylon 66, are more susceptible to attack than other polymers. Most commerical suppliers of polymeric materials supply data sheets which indicate resistance (and lack thereof) to common solvents. 

Ethynes are industrially used as a starting material for polymers, e.g. vinyl flooring, plastic piping. Teflon and acrylics. Polymers are large molecules, which are prepared hy linking many small monomers. Polyvinyl chloride, also commonly known as PVC, is a polymer produced from the polymerization of vinyl chloride. 

Polymerized vinyl chloride as a homopolymer is hard and brittle, making it difficult to work and impractical as a commercial material. In 1926, Waldo Lonsbury Semon (1898—1999) was working for B. F. Goodrich searching for a synthetic rubber that could adhere to metal objects. Semon examined vinyl chloride and found that when polyvinyl chloride powder was mixed in certain solvents, he obtained a stiff gel that could be molded into a plastic material. The material s hardness and pliability depended on the mix of solvent and polyvinyl chloride. Semon... 

Sodium ion-selective field-effect transistors (Na+ ISFETs) were prepared by using three different types of polymeric matrix materials, such as polyvinyl chloride, bio-compatible polymer (polyurethane) and Urushi (natural oriental lacquer). Their electrochemical characteristics were discussed in connection with their characteristics of polymeric matrix membranes. 

ACS, Polymeric Materials Science Engineering Fall Meeting 1999. Volume 81. Conference proceedings. New Orleans, La., 22nd-26th Aug.1999, p.542-3 SILANE-MODIFIED POLYVINYL CHLORIDE PERVAPORATION MEMBRANES Silverstein M S Sluszny A Narkis M Technion-Israel Institute of Technology (ACS,Div.of Polymeric Materials Science Engng.)... 

The chemicals used for coating and laminating are polymeric materials, either naturally occurring or produced synthetically. These include natural and synthetic rubbers, polyvinyl chloride, polyvinyl alcohol, acrylic, phenohc resins, polyurethanes, silicones, fluorochemicals, epoxy resins and polyesters." Coating formulations typically include auxiliaries such as plasticizers, adhesion promoters, viscosity regulators, pigments, fillers, flame retardants, catalysts and the like. ... 

Giving the vinyl group a name allows chemists to use simple trivial names for compounds like vinyl chloride, the material that polymerizes to give PVC (polyvinyl chloride) but the importance of the name lies more in the difference in reactivity (Chapter 17) between vinyl and allyl groups. 

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). 

Most UF membranes are made from polymeric materials, such as, polysulfone, polypropylene, nylon 6, PTFE, polyvinyl chloride, and acryhc copolymer. Inorganic materials such as ceramics, carbon-based membranes, and zirconia, have been commercialized by several vendors. The important characteristics for membrane materials are porosity, morphology, surface properties, mechanical strength, and chemical resistance. The membrane is tested with dilute solutions of well-characterized macromolecules, such as proteins, polysaccharides, and surfactants of known molecular weight and size, to determine the MWCO. 

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