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Copolymers polyphenylenes

Ethylene Chlorotrifluoroethylene Copolymer Polyphenylene Ether, Modified 9... [Pg.1594]

Common conductive polymers are poly acetylene, polyphenylene, poly-(phenylene sulfide), polypyrrole, and polyvinylcarba2ole (123) (see Electrically conductive polymers). A static-dissipative polymer based on a polyether copolymer has been aimounced (124). In general, electroconductive polymers have proven to be expensive and difficult to process. In most cases they are blended with another polymer to improve the processibiUty. Conductive polymers have met with limited commercial success. [Pg.296]

The main experimental techniques used to study the failure processes at the scale of a chain have involved the use of deuterated polymers, particularly copolymers, at the interface and the measurement of the amounts of the deuterated copolymers at each of the fracture surfaces. The presence and quantity of the deuterated copolymer has typically been measured using forward recoil ion scattering (FRES) or secondary ion mass spectroscopy (SIMS). The technique was originally used in a study of the effects of placing polystyrene-polymethyl methacrylate (PS-PMMA) block copolymers of total molecular weight of 200,000 Da at an interface between polyphenylene ether (PPE or PPO) and PMMA copolymers [1]. The PS block is miscible in the PPE. The use of copolymers where just the PS block was deuterated and copolymers where just the PMMA block was deuterated showed that, when the interface was fractured, the copolymer molecules all broke close to their junction points The basic idea of this technique is shown in Fig, I. [Pg.223]

Fig. 11. Effect of polyolefin primers on bond strength of ethyl cyanoacrylate to plastics. All assemblies tested in accordance with ASTM D 4501 (block shear method). ETFE = ethylene tetrafluoroethylene copolymer LDPE = low-density polyethylene PFA = polyper-fluoroalkoxycthylene PBT = polybutylene terephthalate, PMP = polymethylpentene PPS = polyphenylene sulfide PP = polypropylene PS = polystyrene PTFE = polytetrafluoroethylene PU = polyurethane. From ref. [73]. Fig. 11. Effect of polyolefin primers on bond strength of ethyl cyanoacrylate to plastics. All assemblies tested in accordance with ASTM D 4501 (block shear method). ETFE = ethylene tetrafluoroethylene copolymer LDPE = low-density polyethylene PFA = polyper-fluoroalkoxycthylene PBT = polybutylene terephthalate, PMP = polymethylpentene PPS = polyphenylene sulfide PP = polypropylene PS = polystyrene PTFE = polytetrafluoroethylene PU = polyurethane. From ref. [73].
MPPO Modified polyphenylene oxide PP-co-PE Ethylene/propylene copolymer... [Pg.762]

Engineering polymers are often used as a replacement for wood and metals. Examples include polyamides (PA), often called nylons, polyesters (saturated and unsaturated), aromatic polycarbonates (PCs), polyoxymethylenes (POMs), polyacrylates, polyphenylene oxide (PPO), styrene copolymers, e.g., styrene/ acrylonitrile (SAN) and acrylonitrile/butadiene/styrene (ABS). Many of these polymers are produced as copolymers or used as blends and are each manufactured worldwide on the 1 million tonne scale. [Pg.66]

Dendrimers, or arborols, or cascade, or cauliflower, or starburst polymers, were first synthesized in the early 1980s [3,4]. In 1985 Tomalia et al. [5] and Newkome et al. [6] presented the first papers dealing with dendrimers. A multitude of dendrimers have been presented in the literature ranging from polyami-doamine [7,8],poly(propylene imine) [9,10], aromatic polyethers [11-13] and polyesters [14, 15], aUphatic polyethers [16] and polyesters [17], polyalkane [18-19], polyphenylene [20], polysilane [21] to phosphorus [22] dendrimers. Combinations of different monomers as well as architectural modifications have also been presented. For example, chirality has been incorporated in dendrimers [23,24]. Copolymers of linear blocks with dendrimer segments (dendrons) [25-27] and block-copolymers of different dendrons have been described [28]. [Pg.5]

Sulfonated poly(4-substituted benzoyl-1,4-phenylene) homopolymers and copolymers using concentrated sulfuric acid or fuming sulfuric acid have been shown to form sulfonated polymers with variable degrees of sulfonation. To improve film formation of the sulfonated polyphenylenes, multiblock copolymers have been synthesized by reacting a more flexible poly(arylene ether sulfone) with sulfonated poly-phenylenes. ... [Pg.361]

The effect of blending LDPE with EVA or a styrene-isoprene block copolymer was investigated (178). The properties (thermal expansion coefficient. Young s modulus, thermal conductivity) of the foamed blends usually lie between the limits of the foamed constituents, although the relationship between property and blend content is not always linear. The reasons must he in the microstructure most polymer pairs are immiscible, but some such as PS/polyphenylene oxide (PPO) are miscible. Eor the immiscible blends, the majority phase tends to be continuous, but the form of the minor phase can vary. Blends of EVA and metallocene catalysed ethylene-octene copolymer have different morphologies depending on the EVA content (5). With 25% EVA, the EVA phase appears as fine spherical inclusions in the LDPE matrix. The results of these experiments on polymer films will apply to foams made from the same polymers. [Pg.4]

PS (polystyrene), PVC [poly(vinyl chloride)], PC (bisphenol A polycarbonate) PMMA [poly (methyl methacrylate)], PB (polybutadiene), SAN (styrene-acrylonitrile copolymer),NBR (acrylonitrile-butadiene rubber), PPE (polyphenylene ether), SBR (styrene-butadiene rubber)... [Pg.366]

Several flexible polymers, such as natural rubber (NR) synthetic rubber (SR) polyalkyl acrylates copolymers of acrylonitrile, butadiene, and styrene, (ABS) and polyvinyl alkyl ethers, have been used to improve the impact resistance of PS and PVC. PS and copolymers of ethylene and propylene have been used to increase the ductility of polyphenylene oxide (PPO) and nylon 66, respectively. The mechanical properties of several other engineering plastics have been improved by blending them with thermoplastics. [Pg.131]

Propylene oxide is one of the raw materials used to manufacture rubbery and crystalline polyepoxides. R. J. Herold and R. A. Livigni describe propylene oxide polymerization with hexacyanometalate salt complexes as catalyst. Polyphenylene oxide is made by copper catalyzed oxidative coupling of 2,6-dimethylphenol. G. D. Cooper, J. G. Bennett, and A. Factor discuss the preparation of copolymers of PPO by oxidative coupling of dimethylphenol with methylphenylphenol and with diphenylphenol. [Pg.11]

Polyurethane-based FTPEs are produced by reacting fluorinated polyether diols with aromatic disocyanates. The resulting block copolymers contain fluorinated polyether soft segments.68 Another possible method of preparation of fluorinated TPE is dynamic vulcanization. Examples are a blend of a perfluoroplastic and a perfluoroelastomer containing curing sites or a combination of VDF-based fluo-roelastomers and thermoplastics, such as polyamides, polybutylene terephtalate, and polyphenylene sulhde.69 70... [Pg.156]

Polystyrene is one of the most widely used thermoplastic materials ranking behind polyolefins and PVC. Owing to their special property profile, styrene polymers are placed between commodity and speciality polymers. Since its commercial introduction in the 1930s until the present day, polystyrene has been subjected to numerous improvements. The main development directions were aimed at copolymerization of styrene with polar comonomers such as acrylonitrile, (meth)acrylates or maleic anhydride, at impact modification with different rubbers or styrene-butadiene block copolymers and at blending with other polymers such as polyphenylene ether (PPE) or polyolefins. [Pg.25]

MABS polymers (methyl methacrylate-acrylonitrile-butadiene-styrene) together with blends composed of polyphenylene ether and impact-resistant polystyrene (PPE/PS-I) also form part of the styrenic copolymer product range. Figure 2.1 provides an overview of the different classes of products and trade names. A characteristic property is their amorphous nature, i.e. high dimensional stability and largely constant mechanical properties to just below the glass transition temperature, Tg. [Pg.26]

FIGURE 9.4 Dependence of constants (a, b, and c present Henry constant, sorption affinity constant, and Langmuir sorption capacity respectively) of the model of dual-mode sorption of hydrocarbons by glassy polyphenylene oxides on boiling temperatures of hydrocarbons Z), is pDMePO, poly-2,6-dimethyl-l,4-phenylene oxide o is pDPhPO, poly-2,6-diphenyl-l,4-phenylene oxide is pDMePO/pDPhPO copolymer (97.5/2.5% mol) v is pDMePO/pDPhPO copolymer (75/25% mol). (From analysis of results presented in Lapkin, A.A., Roschupkina, O.P., and Ilinitch, O.M., J. Membr. Sci., 141, 223, 1998.)... [Pg.237]

For the devices presented here, the wrapped copolymer PPyVPV and a wrapped copolymer of poly thiophene and polyphenylene derivative, PTP, were used as the emitting materials SPAN and EB were used as the redox materials ITO and Al were used as electrodes. Figure 9.11 shows the schematic diagram of the device structure of the color-variable bipolar/ac light-emitting devices. [Pg.257]

ETFE 8 General Purpose Polystyrene 6-9 HDPE 8 Impact Polystyrene 9 lonomer 8 LDPE 8 MDPE 8 Polyimide 7 Polymethylpentene 8 Polyphenylene Sulfide 8 Polypropylene 5-9 PVC 8 PVDC 7 SAN Copolymer 5-9 UHMWPE 8 Aluminum Chlorohydroxide elevated temoerature ... [Pg.943]


See other pages where Copolymers polyphenylenes is mentioned: [Pg.148]    [Pg.230]    [Pg.389]    [Pg.97]    [Pg.148]    [Pg.338]    [Pg.41]    [Pg.31]    [Pg.287]    [Pg.95]    [Pg.453]    [Pg.254]    [Pg.148]    [Pg.5]    [Pg.7]    [Pg.643]    [Pg.56]    [Pg.159]    [Pg.14]    [Pg.210]    [Pg.26]    [Pg.99]    [Pg.367]    [Pg.42]    [Pg.491]    [Pg.23]    [Pg.254]    [Pg.293]    [Pg.8]   
See also in sourсe #XX -- [ Pg.81 ]




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Polyphenylenes

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