Polyvinyl chloride thermal

Anderson, R.C. Alarie, Y. "Acute Lethal Effects of Polyvinyl-chloride Thermal Decomposition Products in Normal and Cannulated Mice, Abstracts... 

Wong KL, Stock F, Alarie YC. 1983. Evaluation of the pulmonary toxicity of plasticized polyvinyl chloride thermal decomposition products in guinea pigs by repeated CO2 challenges. Toxicol Appl Pharmacol 70 236-248. 

Polyvinyl chloride (p.v.c.) P.V.C. is one of the two most important plastics in terms of tonnage and shows many properties typical of rigid amorphous thermoplastics. More individually, it softens at about 70°C, burns only with difficulty and is thermally unstable. To reduce this instability, stabilisers are invariably compounded into the polymer. 

The most common backbone structure found in commercial polymers is the saturated carbon-carbon structure. Polymers with saturated carbon-carbon backbones, such as polyethylene, polypropylene, polystyrene, polyvinyl chloride, and polyacrylates, are produced using chain-growth polymerizations. The saturated carbon-carbon backbone of polyethylene with no side groups is a relatively flexible polymer chain. The glass transition temperature is low at -20°C for high-density polyethylene. Side groups on the carbon-carbon backbone influence thermal transitions, solubility, and other polymer properties. 

Thermal Effects in Addition Polymerizations. Table 13.2 shows the heats of reaction (per mole of monomer reacted) and nominal values of the adiabatic temperature rise for complete polymerization. The point made by Table 13.2 is clear even though the calculated values for T dia should not be taken literally for the vinyl addition polymers. All of these pol5Tners have ceiling temperatures where polymerization stops. Some, like polyvinyl chloride, will dramatically decompose, but most will approach equilibrium between monomer and low-molecular-weight polymer. A controlled polymerization yielding high-molecular-weight pol)mier requires substantial removal of heat or operation at low conversions. Both approaches are used industrially. 

This comprehensive article supplies details of a new catalytic process for the degradation of municipal waste plastics in a glass reactor. The degradation of plastics was carried out at atmospheric pressure and 410 degrees C in batch and continuous feed operation. The waste plastics and simulated mixed plastics are composed of polyethylene, polypropylene, polystyrene, polyvinyl chloride, acrylonitrile butadiene styrene, and polyethylene terephthalate. In the study, the degradation rate and yield of fuel oil recovery promoted by the use of silica alumina catalysts are compared with the non-catalytic thermal degradation. 9 refs. lAPAN... 

Thermal stabilizers combat degradation by removing the hydrogen chloride that is generated. Additionally, we treat polyvinyl chloride more gently than we do polyolefins. We use milder processing conditions (lower temperatures and lower shear rates) and add lubricants to... 

Polyvinyl chloride resin, because of its inherent thermal instability and wide range of applications, requires us to develop additive recipes based on specific application and processing requirements. Typical additive packages include stabilizers, plasticizers, waxes, processing aids, pigments, and mineral additives. 

The Roles of Hydrogen Chloride in the Thermal and Photochemical Degradation of 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 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. 

Polyvinyl chloride is processed into a number of forms by including additives. Additives are used to vary the properties of PVC so that it can be made soft and flexible or hard and rigid. Additives are also used to inhibit decomposition as a result of exposure to sunlight, ozone, and chemicals. Plasticizers are the primary additive included in PVC materials. Di(2-ethylhexyl) phthalate (DEHP) and a host of other phthalates are the most common plasticizers. Plasticizers impart flexibility, thermal stability, strength, and resilience to PVC compounds. PVCs without plasticizers are classified as UPVC the letters stand for unplasticized polyvinyl chloride. UPVC is rigid and used for conduit, containers, gutters, and floor tiles. Other common PVC additives are biocides, lubricants, and pigments. 

Polyvinyl Chloride. It is well-known how various attempts have been made to stabilise PVC against dehydrochlorination by salts, usually of divalent metal ions - as long chain alkylcarboxylates of Cd(II), Ba(U), Zn(II) [96]. Biswas and Moitra [102] recently established that the 3d metal ions incorporated in PVC-DMG-complex enhance the thermal stability of PVC in the order. 

Polyvinyl Halides. Chlorinated Polyvinyl Chloride It was produced in Germany up to three decades ago, but this was primarily a 1,1-disubstituted product of increased solubility for dry-spinning of fibers. Goodrich has developed a light-activated suspension chlorination process which produces 1,2-dichlorinated structures of increased hot strength, thermal stability, and flame resistance. 

Lead compounds are generally added to polyvinyl chloride in electrical formulations in order to stabilize them against thermal decomposition 7 p.h.r. of National Lead Tribase XL modified tribasic lead sulfate was used throughout the present study. Since the stabilizer itself is an ionic impurity, it is remarkable to note that it actually increases volume resistivity (Table IV). 

Vinyl Chloride. [CAS 75-fl I -4. This compound is produced by alkaline dehydrnchlorinaiion of ethylene dichloride, or by thermal cracking of EDC, or l.l-dichloroethane. Vinyl chloride is polymerized in various ways to polyvinyl chloride (PVC). It is also copolymerized with various other monomers to make a variety of useful resins. The copolymers with about J to 20vinyl acetate are the most important. Demand for vinyl chloride is high, approximating 8 billion pounds (3.6 billion kilograms) per year. 

The authors demonstrated that polyvinyl chloride segments of these graft and block copolymers are more stable than PVC homopolymers prepared according to traditional ways. These last ways lead to disproportionation reactions giving unsaturations at the ends of polymers and these ends are responsible for the poor thermal stability of the polymers. In the present method, termination occurring essentially by transfer reaction, no unsaturations are observed and the authors showed an improvement in stability of the PVC segments of about 20 °C (Scheme 39). 

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