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Polyethylene stabilization

Table 6 Temperature Effect on Thermal Destruction of Polyethylene Stabilized by Fiberglass of Varying Alkalinity... Table 6 Temperature Effect on Thermal Destruction of Polyethylene Stabilized by Fiberglass of Varying Alkalinity...
Figure 5. High-density polyethylene (2% rutile Ti02, 0.5% LS). Elongation retention as a function of 45° south direct Florida exposure for high density polyethylene stabilized with 0.50% of various light stabilizers. Pigmented rutile TiOt. Figure 5. High-density polyethylene (2% rutile Ti02, 0.5% LS). Elongation retention as a function of 45° south direct Florida exposure for high density polyethylene stabilized with 0.50% of various light stabilizers. Pigmented rutile TiOt.
Fig. 62. Kinetics of the increase in carbonyl groups (> C = O) in the photodestruction of polyethylene. 1) Low-pressure polyethylene 2) high-pressure polyethylene 3) high-pressure polyethylene stabilized with a mixture of phenyl-0 -naphthylamine, diphenyl-p-phenylenediamlne, and carbon black. Fig. 62. Kinetics of the increase in carbonyl groups (> C = O) in the photodestruction of polyethylene. 1) Low-pressure polyethylene 2) high-pressure polyethylene 3) high-pressure polyethylene stabilized with a mixture of phenyl-0 -naphthylamine, diphenyl-p-phenylenediamlne, and carbon black.
Kozlov, G. V, Ovcharenko, E. N., Zaikov, G. E. (2008). The Fractal Model of Modified Polyethylene Stability to Cracking. Teoreticheskie Ocnovy Khimicheskoi Tekhnolo-gii, 42(4), 453-456. [Pg.182]

Figure 13.24 Oxidation temperature (from dynamic data) as a function of OIT for a medium-density polyethylene stabilized with a hindered phenol. Drawn after data from Karlsson, Assargren and Gedde (1990). Figure 13.24 Oxidation temperature (from dynamic data) as a function of OIT for a medium-density polyethylene stabilized with a hindered phenol. Drawn after data from Karlsson, Assargren and Gedde (1990).
E. Richaud, X. Colin, C. Monchy-Leroy, L. Audouin, J. Verdu. Polyethylene stabilization against thermal oxidation by a trimethylquinoleine oligomer. Polymer Degradation and Stability 9A(3), 410-420 (2009). [Pg.86]

Physical Stabilization Process. Cellulai polystyrene [9003-53-6] the outstanding example poly(vinyl chloride) [9002-86-2] copolymers of styrene and acrylonitrile (SAN copolymers [9003-54-7]) and polyethylene [9002-88-4] can be manufactured by this process. [Pg.405]

Heat stabilizers protect polymers from the chemical degrading effects of heat or uv irradiation. These additives include a wide variety of chemical substances, ranging from purely organic chemicals to metallic soaps to complex organometaUic compounds. By far the most common polymer requiring the use of heat stabilizers is poly(vinyl chloride) (PVC). However, copolymers of PVC, chlorinated poly(vinyl chloride) (CPVC), poly(vinyhdene chloride) (PVDC), and chlorinated polyethylene (CPE), also benefit from this technology. Without the use of heat stabilizers, PVC could not be the widely used polymer that it is, with worldwide production of nearly 16 million metric tons in 1991 alone (see Vinyl polymers). [Pg.544]

Rigid Applications. The use of the lead stabilizers is very limited in the United States but, they are stiU used in several rigid PVC appHcations in Europe and Asia. The highest use of lead stabilizers in rigid PVC is for pipe and conduit appHcations. Tribasic lead sulfate is the primary heat stabilizer with lead stearates included to provide lubrication. The lead products are typically fully formulated, usually including lubricants and pigments for pipe extmsion appHcations. These lead one-packs, when used at about 1.8—2.5 phr, provide all of the stabilizer and lubrication needed to process the polymer. A lead one-pack contains tribasic lead sulfate, dibasic lead stearate calcium stearate, polyethylene wax, paraffin wax, ester wax, and pigments. [Pg.552]

Triisopropan olamine is used in natural mbber cross-linking and as a color stabilizer for polyethylene formulations. Chain termination of polybutadiene with triisopropan olamine gives improved cold-flow properties. [Pg.11]

Substituted amides (not of the alkanolamide variety) are sold to diverse low volume markets. They have some utility ki polymers such as polyethylene, ethylene-vinyl acetate copolymers, acryUc polymers, PVC, polyamides, and polyesters. They have been found effective as pharmaceutical processkig aids, defoamers (qv), antimicrobials, pesticides, kisect repellents, dispersion stabilizers, and corrosion inhibitors. [Pg.186]

Antioxidants. The 1,2-dihydroquinolines have been used in a variety of ways as antioxidants (qv). For example, l,2-dihydro-2,2,4-trimethylquinoline along with its 6-decyl [81045-48-9] and 6-ethoxy [91-53-2] derivatives have been used as antio2onants (qv) and stabilizers (68). A polymer [26780-96-1] of l,2-dihydro-2,2,4-trimethylquinoline is used in resins, copolymers, lubricant oils, and synthetic fibers (69). These same compounds react with aldehydes and the products are useful as food antioxidants (70). A cross-linked polyethylene prepared with peroxides and other monomers in the presence of l,2-dihydro-6-ethoxyquinoline produces polymers with a chemically bonded antioxidant (71). [Pg.393]

Nearly all polymeric materials require the addition of antioxidants to retain physical properties and to ensure an adequate service life. The selection of an antioxidant or system of antioxidants is dependent upon the polymer and the anticipated end use. A product that will not be exposed to the elements for a long period of time such as polyethylene grocery bags does not need a long term stabilizer polyethylenes used to iasulate communication cable must be stabilized for many years of service. [Pg.228]

Polyolefins. Low concentrations of stabilizers (<0.01%) are added to polyethylene and polypropylene after synthesis and prior to isolation to retard oxidation of the polymers exposed to air. [Pg.228]

Ozonc-rcsjstant elastomers which have no unsaturation are an exceUent choice when their physical properties suit the appHcation, for example, polyacrylates, polysulfides, siHcones, polyesters, and chlorosulfonated polyethylene (38). Such polymers are also used where high ozone concentrations are encountered. Elastomers with pendant, but not backbone, unsaturation are likewise ozone-resistant. Elastomers of this type are the ethylene—propylene—diene (EPDM) mbbers, which possess a weathering resistance that is not dependent on environmentally sensitive stabilizers. Other elastomers, such as butyl mbber (HR) with low double-bond content, are fairly resistant to ozone. As unsaturation increases, ozone resistance decreases. Chloroprene mbber (CR) is also quite ozone-resistant. [Pg.238]

Siding. The resin most used for siding is poly(vinyl chloride) homopolymer, compounded with modifiers, stabilizers, and pigments. Modifiers are most often acryhc esters, followed by chlorinated polyethylene or ethylene—vinyl acetate, used at 6—8 phr (parts per hundred resin). The modifier increases the impact strength of the rigid PVC. [Pg.334]

The demands on insulating materials in soil and fresh water are relatively low. Anodically evolved oxygen makes the use of aging-resistant insulating materials necessary. These consist of special types of rubber (neoprene) and stabilized plastics of polyethylene, and polyvinylchloride, as well as cast resins such as acrylate, epoxy, polyester resin and many others. [Pg.217]

PL can be used as a sensitive probe of oxidative photodegradation in polymers. After exposure to UV irradiation, materials such as polystyrene, polyethylene, polypropylene, and PTFE exhibit PL emission characteristic of oxidation products in these hosts. The effectiveness of stabilizer additives can be monitored by their effect on PL efficiency. [Pg.379]


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See also in sourсe #XX -- [ Pg.318 ]




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