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Copolymer compounds

Copolymers of chlorotrifluoroethylene and ethylene were introduced by Allied Chemicals under the trade name Halar in the early 1970s. This is essentially a 1 1 alternating copolymer compounded with stabilising additives. The polymer has mechanical properties more like those of nylon than of typical fluoroplastic, with low creep and very good impact strength. Furthermore the polymers have very good chemical resistance and electrical insulation properties and are resistant to burning. They may be injection moulded or formed into fibres. [Pg.375]

In addition to the broad categories of TPs and TSs, TPs can be further classified in terms of their structure, as either crystalline, amorphous, or liquid crystalline. Other classes (terms) include elastomers, copolymers, compounds, commodity resins, engineering plastics, or neat plastics. Additives, fillers, and reinforcements are other classifications that relate directly to plastics properties and performance. [Pg.340]

High Vinyl Poly(Bd) SBS Block Copolymer Compound with 30%... [Pg.420]

A modification of the condensation copolymer compounds involves incorporating anionic character into the polymer chain by use of sulfonated monomers. The necessary hydrophilicity is provided by the sulfonated blocks (Fig. 7.8). Like the other polyester condensation polymers, these anionic products can be applied by exhaust or padding. The exhaustion efficiency can be significantly improved by adding small amounts of magnesium chloride to the application bath. [Pg.93]

C CP/MAS spectroscopy is a convenient prehminary tool proving the formation of the IC [20,21]. Using this simple technique, it was possible to confirm the formation of CD inclusion complexes with many different copolymer compounds, e.g. PPO-PEO-PPO [22], PEO-poly[(i )-3-hydroxybutyrate]-PEO [23], PCL-PPG-PCL [24], as well as ferrocene derivatives [25] as guest molecules. Recently, C and Si CP/MAS sohd state NMR spectra were used for characterization of the inclusion complex of polysilsesquioxane with P-cy-clodextrin [26]. SaalwSchter reported using H Fast-MAS sohd state NMR techniques for elucidating the dynamics of the poly(dimethylsiloxane) (PDMS) in-... [Pg.97]

New diene copolymers can be expected. Butadiene-acrylic acid and butadiene-methylvinylp3mdine copolymers have been reported. One of the former copolymers, compounded with zinc oxide, formed a vulcanizate with a tensile strength of over 8,000 psi, the highest on record. The latter copol3rmer has been quaternized with active halogen compounds to form a new type of elastomeric material. ... [Pg.1035]

General Description Kraton Polymers are a range of unhydrogenated styrenic block copolymers, compounds with an unsaturated rubber midblock (styrene-butadiene-styrene [SBS] and styrene-isoprene-styrene [SIS])J ° ]... [Pg.177]

Reactor TPO Reactor TPOs made by sequential copolymerization of PP and EP copolymer Compounding with fillers and additives needed Excellent dispersion Lower need for rubber than compounded TPO Improved melt-flow Need special catalyst and reactor technologies Somewhat higher cost Reactor elastomer may not be quite as efficient as compounded TPO for low temperature toughness... [Pg.1759]

The vulcanized properties of a number of tread rubber candidates including the block copolymers, compounded in a HAF tread compound are shown in Table 1. [Pg.25]

Process Analysis - Diffusion. - Water diffusion in methacrylate based copolymer hydrogels and incorporaion of vitamin B12, aspirin or chlorhexidine Diacetate into such copolymer hydrogels were investigated." The diffusion of water into cylinders of poly-2-hydroxyethyl methacrylate (PHEMA) and copolymers of (HEMA) with tetrahydrofurfuryl methacrylate (THFMA), butyl- methacrylate (BMA), and cyclohexyl methacrylate (CHMA) were studied over a range of copolymer compounds." The diffusion of water into the polymers was found to follow a Fickian, or case 1 mechanism. The diffusion coefficients of water were determined from mass measurements and NMR imaging studies. They were found to vary from 1.7 0.2 x 10 " m s for polyHEMA at 37°C to lower values for the copolymers. The mass of water absorbed at equilibrium relative to the mass of dry polymer varied from 52-58 wt% for polyHEMA to lower values for the copolymers. [Pg.492]

Optimum high temperature color stability for copolymer compounds 0.5 phr Naugard XLl 0.5 phr Naugard 10... [Pg.203]

Most plasticizers have a significant negative impact on the physical properties and compression set of copolymer compounds. Trimellitates, like Plasthall 810TM, ADK Cizer C-9N, and UL-100, or polyester plasticizer Plasthall P670, have performed best in copolymers. The use of these plasticizers in copolymer compounds should be limited to 5-10 phr to minimize interference with peroxide curing systems. [Pg.208]

As a result, the way a copolymer compound is formulated differs considerably from that of the terpolymer. Since stabilization is necessary, Naugard 445 is added, but at a 1 phr level. The Armeen 18D level remains at 0.5 phr, the stearic acid level is held around 1 phr, and if possible, the Vanfre VAM is eliminated. Vanfre should be added to a peroxide-cured copolymer if release is a problem, and then at the minimum level necessary. [Pg.215]

Sheet-off imU rolls must be kept cool to eliminate sticking to the rolls. Zinc and calcium stearate, and metal oxide dusting agents should be avoided with terpolymers because of the potential for forming ionic crosslinks. Soapstone, talc. Crystal 2000, or other commercially available dusting agents that do not contain divalent metal ions can be used. AEM copolymer compounds can be dropped from the internal mixer at 5°C to 10°C higher than terpolymer compounds. [Pg.216]

Chem. Descrip. Alkoxylated copolymer compounded with a hydrophobe Uses Surf, tension mrfoifier and antifoam/defoamerfor semi-syn. and syn. metalworking compds. [Pg.471]

The combination of Uvasorb HA88 FD and Uvasorb HA77 DF gives very high light stability to polyolefins tapes and to the talc filled Polypropylene copolymer compounds usually used for automotive applications. [Pg.95]


See other pages where Copolymer compounds is mentioned: [Pg.56]    [Pg.314]    [Pg.284]    [Pg.352]    [Pg.523]    [Pg.75]    [Pg.536]    [Pg.86]    [Pg.165]    [Pg.89]    [Pg.118]   


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