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Polyvinylchloride compounds

Panchal J, et al. Effect of hyperdispersants in polyethylene masterbatch and rigid polyvinylchloride compound. ANTEC 2007, conference proceedings. Society of Plastics Engineers 2007. [Pg.266]

EFFECT OF HYPERDISPERSANTS IN POLYETHYLENE MASTERBATCH AND RIGID POLYVINYLCHLORIDE COMPOUND... [Pg.395]

SOLSPERSE 3000, a hyperdispersant originally developed for the dispersion of titanium dioxide in airdrying paints [5], was identified as showing benefit in the processing of rigid Polyvinylchloride compound. In the case of the Polyethylene masterbatch study, a novel hyperdispersant, SOLPLUS DP310 was developed. This hyperdispersant optimizes both the polymer chain chemistry and the molecular weight to achieve effective dispersion. [Pg.396]

The compounds obtained in solid state have the general formula [MefSCNf JR., (R-cations of cyanine dyes) and could be embedded into polyvinylchloride matrix. Using the matrix as work element of electrodes shows the anionic function concerning the anionic thiocyanate complexes of Pd, Hg, Zn and the response to sepai ately present thiocyanate and metallic ions is not exhibited. [Pg.35]

A better combination of fiber and polymer is achieved by an impregnation of [44] the reinforcing fabrics with polymer matrixes compatible with the polymer. Polymer solutions [40,45] or dispersions [46] of ]ow viscosity are used for this purpose. For a number of interesting polymers, the lack of solvents limits the use of the method of impregnation [44]. When cellulose fibers are impregnated with a bytyl benzyl phthalate plasticized polyvinylchloride (PVC) dispersion, excellent partitions can be achieved in polystyrene (PS). This significantly lowers the viscosity of the compound and the plasticator and results in cosolvent action for both PS and PVC [46]. [Pg.796]

Di- and mono-esters of phthalic acid, an ortho-dicarboxylic acid derivative of benzene. These compounds are widely used as industrial plasticizers to coat polyvinylchloride surfaces of plastics used in food packaging and medical devices (iv drip bags, blood storage bags, etc.) and are common environmental contaminants. Several phthalate mono-esters are peroxisome proliferator chemicals and can activate the peroxisome proliferator-activated receptor PPAR. [Pg.976]

Acrylic and allyfic compounds These have been reported to enhance cross-linking in polyvinylchloride [84], PE [85], PP [86], polyisobutylene, and EP copolymers [87], butadiene-styrene copolymers, and NR [88] each compounded with 50 phr of carbon black. [Pg.864]

Highly halogenated organic compounds such as polychlorinated biphenyls and perchloroethylene appear to be too highly oxidised and low in energy content to serve as sources of electrons and energy for microbial metabolism. Bacteria are more likely to use them as electron acceptors in cell-membrane-based respiration processes [154]. The environmental fate of halogenated polymers such as polyvinylchloride or Teflon may depend on the question of whether it will be appropriate to sustain de-halorespiration processes. [Pg.434]

The largest volume of polymeric materials used for wire and cable insulation are thermoplastics, namely, polyethylene (PE) and polyvinylchloride (PVC), and to a lesser degree elastomeric compounds. The main reason for the prevalence of PE and PVC in wire and cable insulation is their easy processing and relatively... [Pg.181]

Xing, B., and J. J. Pignatello, Dual-mode sorption of low-polarity compounds in glassy polyvinylchloride and soil organic matter , Environ. Sci. Technol., 31,792-799 (1997). [Pg.1252]

Pancreas powder, penicillin, pharmaceuticals, phosphate ores, plastics, polyvinylchloride (PVC), potash, potassium compounds, protein pigments, pyrites, pyrocatechol Raisin seeds, reduced ores, refractoiy materials, rice starch, rock salt... [Pg.363]

The principal use of chlorine is in the production of organic compounds. Of these the production of PVC t polyvinylchloride) is probably ihe single largest consumer although chlorinated solvents as a class account for larger tonnage. See also Chlorinated Organics and Polyvinyl Chloride (PVC). [Pg.371]

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). [Pg.313]

A traditional area of application for Pb(OR)2 is also the technology of polymers, where they are recommended for the stabilization of vinyl polymers, polyvinylchloride, and so on. [715, 1271], Cresolate is also used for the purification of oil from sulfur-containing compounds [715], A number of pub-... [Pg.310]

Ethylene glycol (EG) may be obtained from cellulose by many ways, for instance, by the catalytic conversion over carbide catalysts [71], It is the simplest linear polyol available and often serves as a model for more complex substrates. Many reports are therefore available on the telomerization of EG. The possible telomer products are shown in Scheme 14, the linear mono-telomer typically being the desired compound. The mono-telomer can be used, after saturation of the double bonds, as a plasticizer alcohol in polyvinylchloride production, whereas application in cosmetics and surfactants has also been indicated [72]. Early examples include the work of Dzhemilev et al., who first reported on the telomerization of butadiene with EG in 1980, yielding a mixture of the mono- and di-telomers and butadiene dimers using a palladium catalyst activated by AlEt3 [73]. Kaneda also reported the use of EG in... [Pg.66]

Polyvinylchloride (PVC). Kim et al. (H) analyzed the volatiles of polyvinylchloride (PVC), one of the most versatile packaging materials. The major precursors for the formation of the volatile compounds were considered to be PVC polymer, bis-(2-ethylhexyl) adipate (DOA), bis-2-(ethyl hexyl) phthalate (DOP) and tris-nonylphenyl phosphite and epoxidized soybean oil. [Pg.400]

Elements Ge, Sn, and Pb form many interesting varieties of organometallic compounds, some of which are important commercial products. For example, EuPb is an anti-knock agent, and organotin compounds are employed as polyvinylchloride (PVC) stabilizers against degradation by light and heat. Some examples and advances are discussed in the present section. [Pg.549]

The synthesis as well as the recycling and disposal of halogenated compounds such as Polyvinylchloride (PVC), flame retardants (for example Tetrabromobisphenol A), y-Hexachlorocydohexane (y-HCH), Hexachlorobenzene (HCB) leads to the formation of byproducts and residues. Polymers, for example, as well as printed circuit boards or shredder residues include problematic substances which, for ecological reasons, cannot be passed on to the environment but have to be supplied to a specific and proper recycling or disposal process. Prior to this background so called "Supercritical Fluids" are of special interest. Supercritical fluids can be used for the synthesis of polymers in an enviromentally friendly way as well as for recycling and disposal processes. [Pg.163]

The major use of vinyl chloride (also known as vinyl chloride monomer, VCM) is in the production of the ubiquitous plastic, PVC or polyvinylchloride, which began to be used in the 1940s. This polymer is used in a wide variety of products ranging from cling film, bottles, car components, pipes, electrical insulation, and window frames. Unfortunately, vinyl chloride, which is used to make the plastic, is a hazardous chemical. For this reason and because PVC is an organochlorine compound, it has received a bad press. It has important properties, however, such as flexibility, toughness, and durability, that make it an extremely useful and versatile material. [Pg.168]

Funatsu K. and Sato M., "Measurement of slip velocity and normal stress difference of polyvinylchloride, Adv. in Rheol., 4 (Mexico 1984) 465-472. Knappe W. and E. Krumbock, "Evaluation of slip flow of PVC compounds by capillary rheometry," Adv. in Rheol., 3 (Mexico 1984) 417-424. de Smedt C., Nam S., "The processing benefits of fluoroelastomer appUcation in LLDPE," Plast. Rubber Process. Appl. 8,11 (1987). [Pg.387]

At temperatures below 240 °C, there is essentially no gas evolution, with the exception of some HjO after long heating time. In the range 250-300 °C, small amounts of low hydrocarbons (AN, MAN, propionitrile) evolve. These compounds are supposed to proceed from depolymerization of uncyclized parts of the polymer. Hydrogen cyanide starts to evolve after 70 min at 250 °C and after 30 min at 300 °C. The early evolution of HCN has frequently been ascribed to dehydrocyanation (analog to dehydrochlorination from polyvinylchloride), either within a molecule, leading to unsaturation ... [Pg.25]


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See also in sourсe #XX -- [ Pg.79 ]




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