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Polyolefins light stabilizers

The 2-imino-4-thiazolines may be used as ultraviolet-light stabilizers of polyolefin compositions (1026). 2-Aminothiazole improves adhesive properties of wood to wood glue (271). Cbmpound 428 exhibits antioxidant properties (Scheme 242) (1027). Ammonium N-(2-thiazolyl)dithio-carbamate (429) is a bactericide and fungicide used in industrial products such as lumber, paint, plastics, and textiles (1037). Compound 430 is reported (1038) to form an excellent volume of foam coating in aluminum pans when ignited with propane. [Pg.170]

Sesamex [51-14-9] (Sesoxane) (30) is a synergist oflow toxicity, acute oral LD q (rat) = 2000 2270 mg/kg, for pyrethrins and allethrin. 6,7-Dihydroxy 4-methylcoumarin has been offered as an antioxidant for phenoHcs and polymers, and as an anthelmintic. 2,4,5-Trihydroxybutyrophenone has been available as an antioxidant and light stabilizer for polyolefins, waxes, and foods. Isoflavones, eg (31), have been patented as components of antioxidant compositions for foods and cosmetics (qv) (97). [Pg.381]

Hindered Amines. Hiadered amines are extremely effective ia protecting polyolefins and other polymeric materials against photodegradation. They usually are classified as light stabilizers rather than antioxidants. [Pg.226]

It has been only found that some antioxidants and light stabilizers show the ability for partial inhibition of thermal destruction of the polyolefins. [Pg.83]

Organic phosphites POR(OR )OR where R=Ci—C30 represents aliphatic, cycloaliphatic, or aromatic radical, are also able of inhibiting the thermal destruction of polyolefin [19]. Of light stabilizers, benzo-phenone derivatives have the ability for inhibiting thermal destruction of polyolefins, too. [Pg.83]

Light stabilizers improve the long-term durability of plastics, especially polyolefins. Polymeric hindered amines, such as Tinuvin 622, and Chimasorb 944, are commonly used in polyolefins as light stabilisers. [Pg.325]

The hindered-amine light stabilizers for polymers are piperidine derivatives. An example of these products is bis-(2.2,6,6-tetramethyl-4-pipendinyl)sebaeale, tradenained Tinuviii 770, useful as a light stabilizer for polyolefins and styrenics. [Pg.1389]

PY 151, Cl NO. 13980 Yellow H4G Green shade good fastness to light and solvents finds use in PVC and polyolefins heat stability to 425°F... [Pg.119]

The earliest data on solution of stabilizer permanency problems by means of polymerization of functionalized monomers having double bonds C=C were published in the late 1960s. They deal with results concerning stabilization of rubber [50-53] (experience from the chemical modification of rubber were successfully exploited in this case) and with light stabilization of polyolefins [54]. [Pg.87]

Various polyesters derived from phosphorous or phosphoric acids were prepared. Efiicient polyphosphites were synthesised in the early 196(. Polyphosphite prepared from 152 and 4,4 -isopropylidenebis(cyclohexanol) was tested as a thermal stabilizer for PC [199] or as secondary AO for radiation sterilized EPM [200]. Built-in phosphites obtained by transesterification of triallcylphosphite with 4,4 -isopro-pylidenebisphenol or 4,4 -thiobisphenol possess antioxidant properties in polyolefins. Stabilizer containing phosphite moiety 153 was prepared from tris(2-hydroxy-ethyl)isocyanate, decyl alcohol and triphenylphosphite [201]. Various phosphites were derived firom polynuclear phenols or dihydric phenols. For example, a polycondensate prepared by reaction of phosphorus trichloride with 2,5-di-rert-butylhydroquinone was tested as heat and light stabilizer for PP [202], A linear polyester with a built-in phenolic moiety was synthesised from (2,6-di-tm-butyl-4-methylphenyl)bis(6-hydroxyhexyl)phosphite and dimethyl terephthalate [203]. [Pg.109]

A great attention was paid to grafting of light stabilizers onto polyolefins. 2-Hydroxy-4-methacryloyloxybenzophenone was grafted onto LDPE, HDPE, PP, poly(4-methylpent-l-ene) or ABS in extruders in the presence of peroxides or onto LDPE or PP in the melt without peroxide. Grafting on PS was very efficient. [Pg.115]

Poly[styrene-co-(2-hydroxy-4 -vinylbenzophenone)] was less efficient in PS than 2-hydroxy-4-methoxybenzophenone [334]. Similarly, PE films doped with 4-dodecyloxy-2-hydroxybenzophenone (0.1 mol%) were more stable than PE doped with copolymers of ethylene with polymerisable benzophenones having a comparable content of chromophores [54]. The efficiency of a SAN type LS, a terpolymer of 2-hydroxy-4-(4-vinylbenzyloxy)benzophenone with acrylonitrile and styrene did not exceed that of conventional LS [84]. No efficiency loss of 2-hydroxy-4-methacryloyloxybenzophenone in ABS was observed after bonding into a terpolymer with styrene and acrylonitrile. The homopolymer was slightly inferior to both the monomer and terpolymer [84]. A better protection of PP was provided by poly[(2-hydroxy-3-allyl-4-methoxyphenylbenzophenone)-co-dibutyl maleate] than with 2-hydroxy-3-allyl-4-methoxybenzophenone [335] (stabilization tests were performed in the presence of phenolic antioxidants). A comparable or better light stabilizing efficiency of poly[vinyl acetate-co-(5-methylacryloyloxy salicylate)] or poly(2-allylphenyl salicylate-co-dioctyl maleate) than that of alkyl-phenyl salicylates was observed in polyolefins [335]. [Pg.154]

Sevini, E. Marcato, B. Chromatographic determination of some hindered amine light stabilizers in polyolefins. J. Chromatogr. 1983, 260, 507-512. [Pg.397]

Used as a thermo/light-stabilizing phenolic antioxidant in the manufacture (compounding and end use) of white, light-colored, and transparent vulcanizates based on natural or synthetic rubber, PS, polyolefins, and pentaplast. Also used in POM and ABS thermoplastics because of its low volatility and migration properties. [Pg.74]

Polyolefins - An Arrhenius model has been developed for lifetime prediction of the light stability of polypropylene . Photooxidation processes in blends of polypropylene with poly(butylene terephthalate) (PBT) are complicated by the thermal sensitivity of the polypropylene and the screening effect of the terephthalate ester . This effect is shown in Scheme 1. [Pg.357]

Hindered Amine Light Stabilizers (HALS) are a new class of highly efficient stabilizers protecting polyolefins and other polymers against light-induced deterioration. They were initially developed into commercial products in our laboratories. In this review we describe the details of how they were synthesized, evaluated and developed. [Pg.37]

As a partially hindered amine, 3 showed light-stabilizing activity lower than that of piperazine or piperidine HALS, but comparable to commercial benzophenones. Like HALS, they are strongly synergistic with benzophenones and benzotriazoles in polyolefins. [Pg.95]

It is well known that HALS compounds (sterically hindered amine light stabilizers) exert excellent photostabilizing effect on polyolefins (1-3). Most of the authors agree that N-oxyl radicals formed from HALS compounds play an important role in the photostabilizing process (4-6). [Pg.109]

Other alloys with steel and other metals Electroplating Coins and jewelry Nickel-cadmium batteries Catalysts for hydrogenation Light stabilizer in polyolefins... [Pg.69]

This volume is including information about thermal and thermooxidative degradation of polyolefine nanocomposites, modeling of catalytic complexes in the oxidation reactions, modeling the kinetics of moisture adsorption by natural and synthetic polymers, new trends, achievements and developments on the effects of beam radiation, structural behaviour of composite materials, comparative evaluation of antioxidants properties, synthesis, properties and application of polymeric composites and nanocomposites, photodegradation and light stabilization of polymers, wear resistant composite polymeric materials, some macrokinetic phenomena, transport phenomena in polymer matrix, liquid crystals, flammability of polymeric materials and new flame retardants. [Pg.434]


See other pages where Polyolefins light stabilizers is mentioned: [Pg.170]    [Pg.314]    [Pg.17]    [Pg.112]    [Pg.162]    [Pg.715]    [Pg.66]    [Pg.166]    [Pg.477]    [Pg.197]    [Pg.1138]    [Pg.1641]    [Pg.1642]    [Pg.280]    [Pg.92]    [Pg.12]    [Pg.663]    [Pg.153]    [Pg.122]    [Pg.152]    [Pg.155]    [Pg.529]    [Pg.362]    [Pg.37]    [Pg.50]    [Pg.57]    [Pg.59]    [Pg.297]    [Pg.218]   
See also in sourсe #XX -- [ Pg.105 , Pg.114 ]




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