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Polymer substrates polyethylene

Organic photoreceptors can be prepared in either a flexible web or drum format. Webs are usually prepared on polymer substrates, polyethylene tere-phthalate being the most common. The substrates are between 100 to 200 pm in thickness and coated with a conducting surface layer. The substrates often contain layers on the reverse side for reduced curl, static discharge prevention, and control of frictional characteristics. The web configuration is also widely used for laboratory studies. For drums, the substrate is a metal cylinder, usually Al. Recently, however, drums of a poly(phenylene sulfide) resin doped with conductive C black have been developed (Kawata and Hikima, 1996). Drums are widely used in low- and mid-volume applications. Drums, however, are not well suited for research purposes. Thus, the preparation and characterization of drum photoreceptors is usually related to a specific application. [Pg.110]

Sihcone products dominate the pressure-sensitive adhesive release paper market, but other materials such as Quilon (E.I. du Pont de Nemours Co., Inc.), a Werner-type chromium complex, stearato chromic chloride [12768-56-8] are also used. Various base papers are used, including polyethylene-coated kraft as well as polymer substrates such as polyethylene or polyester film. Sihcone coatings that cross-link to form a film and also bond to the cellulose are used in various forms, such as solvent and solventless dispersions and emulsions. Technical requirements for the coated papers include good release, no contamination of the adhesive being protected, no blocking in roUs, good solvent holdout with respect to adhesives appHed from solvent, and good thermal and dimensional stabiUty (see Silicon COMPOUNDS, silicones). [Pg.102]

Friedrich et al. also used XPS to investigate the mechanisms responsible for adhesion between evaporated metal films and polymer substrates [28]. They suggested that the products formed at the metal/polymer interface were determined by redox reactions occurring between the metal and polymer. In particular, it was shown that carbonyl groups in polymers could react with chromium. Thus, a layer of chromium that was 0.4 nm in thickness decreased the carbonyl content on the surface of polyethylene terephthalate (PET) or polymethylmethacrylate (PMMA) by about 8% but decreased the carbonyl content on the surface of polycarbonate (PC) by 77%. The C(ls) and 0(ls) spectra of PC before and after evaporation of chromium onto the surface are shown in Fig. 22. Before evaporation of chromium, the C(ls) spectra consisted of two components near 284.6 eV that were assigned to carbon atoms in the benzene rings and in the methyl groups. Two additional... [Pg.273]

Electric discharge methods are known [31] to be very effective for nonactive polymer substrates such as polystyrene, polyethylene, polypropylene, etc. They are successfully used for cellulose-fiber modification to decrease the melt viscosity of cellulose-polyethylene composites [32] and to improve the mechanical properties of cellulose-polypropylene composites [28]. [Pg.795]

The two polymer substrates investigated as part of the study of DBDPO mixtures were polypropylene (PP) and linear high density polyethylene (HDPE). while both PP and HDPE decompose by similar random chain scission, radical mechanisms, chain transfer occurs much more teadily during the pyrolysis of PP because of the presence of the tertiary hydrogens. In addition, only primary chain end radicals are formed when the HDPE chain cleaves homolytically. Therefore, a comparison of the PP/DBDPO and the HDPE/DBDPO mixtures volatile product distributions was undertaken. [Pg.118]

When the reactions of alkyl bromides (n-Q-Cg) with phenoxide were carried out in the presence of cosolvent catalyst 51 (n = 1 or 2,17 % RS) under triphase conditions without stirring, rates increased with decreased chain length of the alkyl halide 82). The substrate selectivity between 1-bromobutane and 1-bromooctane approached 60-fold. Lesser selectivity was observed for polymer-supported HMPA analogue 44 (5-fold), whereas the selectivity was only 1,4-fold for polymer-supported phosphonium ion catalyst 1. This large substrate selectivity was suggested to arise from differences in the effective concentration of the substrates at the active sites. In practice, absorption data showed that polymer-supported polyethylene glycol) 51 and HMPA analogues 44 absorbed 1-bromobutane in preference to 1-bromooctane (6-7 % excess), while polymer-supported phosphonium ion catalyst 1 absorbed both bromides to nearly the same extent. [Pg.91]

The interfaces formed by evaporating copper, nickel and chromium layers on polystyrene, polyvinyl alcohol, polyethylene oxide, polyvinyl methyl ether, polyvinyl acetate and polymethyl methacrylate have been studied with X-ray photoemission spectroscopy (XPS). At submonolayer coverages of the metals, the peak positions and widths of the metallic electron core levels vary significantly from one polymer substrate to another. Most of... [Pg.349]

Characterizing the mechanisms involved in the photodegradation of the various polymers that compose organic cells offers the advisability of reviewing the majority of the mechanisms involved in the photodegradation of polymers. MDMO and MDMO-PPV can be used as an active layer, whereas polymers like polyethylene terephthalate (PET) are used as substrates, and various materials are sounded for encapsulation PC, ceramic on PC, and nanocomposites. [Pg.571]

Disposable IR cards with a thin polymer film window are available for the qualitative analysis of liquids. (These cards were originally manufactured by 3M , but are now available from International Crystal Laboratories, Garfield, NJ, and other suppliers.) Two polymer substrates are available polytetrafluoroethylene for the 4000-1300 wavenumber region and polyethylene for the lower wavenumber region. The absorption spectra for these two materials are displayed in Fig. 4.19(b) and (c). A thin film can be deposited onto the polymer window by evaporation from solution or by smearing the liquid onto the polymer. A major advantage of these cards is that the polymer films do not dissolve in water therefore... [Pg.247]

For polymer materials, the relatively poor temperatme tolerance is a severe problem that hinders their applications. Common polymer substrates, such as polyethylene and polyethylene terephthalate can only withstand a maximal temperature of 80 and 150"C, respectively. They are obviously too low for high-temperature fabrication methods, such as chemical vapor deposition and thermal annealing. This dilemma is currently compromised by conducting a transfer process where the devices are first fabricated at high... [Pg.6]

One of the principal reasons for failure of the adhesion bonds is a specific adsorption reaction of the medium with the material to be cemented at the boundary with the adhesive. There is an adsorption substitution of adhesive-substrate bonds by medium-substrate bonds. Surface structural defects that are present in each solid are the first to be subjected to adsorption. It is to be expected that the probability of appearance of such defects is higher at an interface of two materials with different properties. The rate of penetration of the medium along the polymer-substrate interface frequently substantially exceeds the rate of diffusion of the medium in pure polymer [212]. Adsorption substitution of the polymer macromolecules by water molecules on the metal surface explains the low water resistance of such adhesive-bonded joints as fluoroplastic-steel or polyethylene-steel [34]. The adhesion strength, which decreases during hold-up of adhesive-bonded joints in water, is frequently reestablished after the joints are dried [213]. [Pg.268]

Spectroscopic methods have been reviewed elsewhere but recent applications of ESCA for study of polymers are interesting. Much of the work in this area has been carried out by Clark, who has reviewed his and other work. " The ESCA method has proved particularly useful for studies of RF plasma modification of polymer surfaces. - Briggs et al. have used X-ray photoelectron spectroscopy to study surface oxidation of polyethylene and its effect on adhesion and Hiraoka and Lee used ESCA to study surface changes in polymers under electron impact and u.v. irradiation. Finally, Ratner et al. used ESCA to follow the grafting of water-compatible polymers into polymer substrates. [Pg.295]

Polymer electrolyte is composed of polymer substrate and metal salt. Possible polymer substrates include polyethylene oxide, poly vinylidene fluoride, poly(methyl methacrylate), polyvinylidene chloride, and polyacrylonitrile. Examples of cations of metal salt are li, Na, K, and Mg. Possible anions are BF, SCN, SO3CF3, AsF PF and NfCFjSOj). An inorganic modifier such as nanopartide Ti02 can be added to increase mechanical properties of supercapadtor. Mass is divided so that polymer substrate is 30 to 90 wt%, metal salt is to 2 to 30 wt%, and nanotube modifier is 3 to 30 wt%. [Pg.237]


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See also in sourсe #XX -- [ Pg.6 ]




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