Polyvinylchloride additives

In the field of plastics, the annual production of polyvinylchloride (PVC) is second only to polyethylene. PVC has long been used in various areas, ranging from agriculture and industry to medical equipment and daily life, due to its well-developed production techniques, easy processing, and low price. However, PVC has its own disadvantages, mainly its low stability toward heat and ultraviolet (UV) light. Also, pure PVC is a very hard material that cannot be easily processed and practically used. Common PVC plastics contain various amounts of plasticizers and other additives, including modifiers, stabilizers, and lubricants. 

II. B polyethylene glycol, ethylene oxide, polystyrene, diisocyanates (urethanes), polyvinylchloride, chloroprene, THF, diglycolide, dilac-tide, <5-valerolactone, substituted e-caprolactones, 4-vinyl anisole, styrene, methyl methacrylate, and vinyl acetate. In addition to these species, many copolymers have been prepared from oligomers of PCL. In particular, a variety of polyester-urethanes have been synthesized from hydroxy-terminated PCL, some of which have achieved commercial status (9). Graft copolymers with acrylic acid, acrylonitrile, and styrene have been prepared using PCL as the backbone polymer (60). 

During WWII, the Germans developed several illuminating mixtures, containing 14-28% of polyvinylchloride (either additionally chlorinated or not) together with 17-35% of magnesium powder, 50-61% of oxidizer and 1 to 5% of vaseline or synthetic wax (Ref 3)... 

When tested in other polymers, maleimides did not affect the rate of cross-linking in polydimethylsiloxane, polyisobutylene, and polyvinylchloride. In polyethylene, the addition of 5 wt.% of m-phenylene dimaleimide increased the G(X) from 1.8 to 7.2. In the polyvinylacetate the effect was even more pronounced the dose for gelation was reduced by about a factor of 50. Contrary to the cross-link enhancing effect found for m-phenylene dimaleimide, cross-linking was retarded in polyvinyl acetate by the addition of monomaleimides. When analyzing the mechanism of the reaction it was concluded that monomaleimides are not expected to affect cross-linking in saturated polymers. ... 

Another important addition polymer is polyvinylchloride (PVC), which is tough and easily molded. Floor tiles, shower curtains, and pipes are most often made of PVC, shown in Figure 12.30. The addition polymer polyvinylidene chloride (trade name Saran), shown in Figure 12.31, is used as plastic wrap for food. The large chlorine atoms in this polymer help it stick to surfaces such as glass by dipole—induced dipole attractions, as we saw in Section 7.1. 

Water uptake in plasticized polyvinylchloride based ion selective membranes is found to be a two stage process. In the first stage water is dissolved in the polymer matrix and moves rapidly, with a diffusion coefficient of around 10 6 cm2/s. During the second stage a phase transformation occurs that is probably water droplet formation. Transport at this stage shows an apparent diffusion coefficient of 2 x 10 8 cm2/s at short times, but this value changes with time and membrane addititives in a complex fashion. The results show clear evidence of stress in the membranes due to water uptake, and that a water rich surface region develops whose thickness depends on the additives. Hydrophilic additives are found to increase the equilibrium water content, but decrease the rate at which uptake occurs. 

In the additive approach, the loss index is increased by placing a high-loss material in contact with a low-loss material. The high-loss material heats and transfers its heat to the low-loss load. Some examples of such additives are carbon black in rubber, NaCl in urea-formaldehyde glue for wood and polyvinylchloride in polyurethane foam (2). 

Infusion sets components (dripping chamber, and infusion line) are produced using different plastic materials, which may vary in their photon absorbing ability [e.g., clear polyvinylchloride (PVC) tubing or opalescent PE tubing]. Additionally, the thickness of the tubing walls also influences the transmission of incident radiation. 

Aqueous solutions of sorbic acid without the addition of antioxidants are rapidly decomposed when stored in polypropylene, polyvinylchloride, and polyethylene containers. 

Hydrocarboxylation of the Ce-Cs a-olefins with cobaltcarbonyl/pyridine catalysts at 200 °C and 20 MPa gives predominantly the linear carboxylic acids. The acids and their esters are used as additives for lubricants. The Ce-Cio a-olefins are hydroformylated to odd-numbered linear primary alcohols, which are converted to polyvinylchloride (PVC) plasticizers with phthalic anhydride. Oligomerization of (preferably) 1 -decene, applying BF3 catalysts, gives oligomers used as synthetic lubricants known as poly-a-olefins (PAO) or synthetic hydrocarbons (SHC) [11, 12]. The C10-C12 a-olefins can be epoxidized by peracids this opens up a route to bifunctional derivatives or ethoxylates as nonionic surfactants [13]. 

Evolved gas analysis, particularly in the form of TGA-DTA-MS, has obvious synthetic polymer applications. It has been applied to study the thermal behavior of homopolymers, copolymers, polymeric blends, composites, residual polymers, solvents, additives, and toxic degradation polymers. In the latter context, hydrogen chloride evolution from heated polyvinylchloride materials is readily quantified by TGA-DTA-MS and such data are of major significance in... 

Thennoplastics are heat softening materials which can be repeatedly heated, made mobile and then reset to a solid state by cooling. Under conditions of fabrication these materials can be moulded (shaped in a mould) by temperature and pressure. Examples of thermoplastics are more numerous than thermosets, e.g. polyethylene, polyvinylchloride, polystyrene, polypropylene, nylon, polyester, polyvinylidene chloride, polycarbonate. Thermoplastics may be further divided into homopolymers which involve one type of monomer, e.g. ethylene polymerised to polyethylene, and copolymers, terpolymers, etc., which involve two or more monomers of different chemical substances. Polymerisation producing thermoplastics and thermoset materials usually follows two basic chemical mechanisms, i.e. condensation and addition polymerisation. 

The thermal volatilization analysis of a mixture of polyvinylchloride and polystyrene is given in Fig. 81. The first peak corresponds to the elimination of HC1 and the second to that of styrene. Dehydrochlorination is retarded in the mixture. The production of styrene is also retarded styrene evolution, in fact, does not occur below 350°C. This contrasts with the behaviour of polyvinylchloride-polymethylmethacrylate mixtures for which methacrylate formation accompanies dehydrochlorination. The observed behaviour implies that, if chlorine radical attack on polystyrene occurs, the polystyrene radicals produced are unable to undergo depolymerization at 300° C. According to McNeill et al. [323], structural changes leading to increased stability in the polystyrene must take place. This could also occur by addition of Cl to the aromatic ring, yielding a cyclohexadienyl-type radical which is unable to induce depolymerization of the styrene chain. 

It can be concluded that our understanding of the photodegradation of polyvinylchloride both in vacuo and in the presence of air is at present limited and that additional work is required. 

Polyvinylchloride (PVC) is commercially the most signihcant member of the family of vinyl resins. The other important members of this group are chlorinated-PVC (CPVC) and polyvinylidene chloride (PVDC). PVC is one of the most widely used, commodity type thermoplastics with an annual consumption of over 5 Mton/y in the USA. The excellent versatility of PVC is attributed to its blending capability with a variety of plasticizers, additives and fillers to yield products ranging from very flexible to very rigid types. In addition, PVC has a low cost advantage and a reasonably good balance of properties, which... 

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