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Copolymers materials

Figure 12.25 The 129Xc diffusion coefficient for Xe absorbed in the copolymer material PBT/PTMO as a function of the diffusion time. One sample was slowly cooled down from the melt and contained many large spherulites. The other was quickly cooled down and contained only small spherulites... Figure 12.25 The 129Xc diffusion coefficient for Xe absorbed in the copolymer material PBT/PTMO as a function of the diffusion time. One sample was slowly cooled down from the melt and contained many large spherulites. The other was quickly cooled down and contained only small spherulites...
The earlier sections of this review have attempted to review the synthesis and characterization of the segmented copolymer materials as well as to highlight fundamental efforts related to a number of structure-property relationships. Polyimide-siloxane copolymers are high performance materials that have been driven by applications frequently identified with aerospace. However, this section will also include surface phenomena which are critical for certain electronic applications and high performance blends utilizing imide-siloxane copolymers. [Pg.89]

Low monomer content PS materials are commercially available with specified styrene monomer levels of 150 ppm (mg/kg) that have actual contents of 100 ppm (ex. BASF O suffix materials 168 NO, 143 IO). These materials can be used for injection molding or extrusion and are priced above normal styrene monomer content materials (those where styrene < 500 mg/kg). High impact polystyrene copolymer materials (HIPS) use normal monomer level polystyrene since there has been no commercial market for such materials. [Pg.427]

The SBS copolymer materials were kindly supplied by the Small Development Company, Torrance, California. The characteristics of the additive-free samples are given in Table I. [Pg.219]

Scheme 2 depicts the two routes to introduction of organic functionality under discussion. The template in each case is a long-chain amine such as M-dodecylamine (we have also used n-decylamine and M-octylamine and other workers have used block copolymer materials as templates) in a solvent system of c. 50 50 ethanol water by volume. Addition of silanes and ageing for c. 18 h at room temperature affords the crude product from which the template can be removed by refluxing in a suitable solvent. [Pg.204]

Based on the tensile impact data in Table IX, we used Run 46 with Aerosol A-196 surfactant to scale up in the pilot plant. We took the 70/30 rubber to copolymer material and diluted it with copolymer to lower the final rubber content to 15% of the polymer this was done during milling. [Pg.282]

The most important monomers for the production of polyolefins, in terms of industrial capacity, are ethylene, propylene and butene, followed by isobutene and 4-methyl-1-pentene. Higher a-olefins, such as 1-hexene, and cyclic monomers, such as norbornene, are used together with the monomers mentioned above, to produce copolymer materials. Another monomer with wide application in the polymer industry is styrene. The main sources presently used and conceivably usable for olefin monomer production are petroleum (see also Chapters 1 and 3), natural gas (largely methane plus some ethane, etc.), coal (a composite of polymerized and cross-linked hydrocarbons containing many impurities), biomass (organic wastes from plants or animals), and vegetable oils (see Chapter 3). [Pg.222]

Some two stage emulsion graft copolymer materials synthesized and characterized by DMS include) the series poly (methyl methacrylate)/poly(n-butyl acrylate) (PMMA/ PnBA) synthesized by Dickie (14) and the series poly(ethyl methacrylate)/poly(n-butyl acrylate) (PEMA/PnBA) synthesized by Sperling et al. (1) The present study will continue the development of the PEMA/PnBA damping materials by incorporating a common comonomer) ethyl acrylate (EA)) in both stages of the emulsion polymerization. [Pg.308]

Of the reported materials, the only commercially available resists are one of the MMA-MAA/MMA-MACl compositions and a t-butyl methacrylate copolymer material (13). In this work, we have chosen to examine the copolymer mixture, which crosslinks at a temperature of 160°C compared to 250 C for the single copolymer. We have carried out experiments to optimize its use for direct write electron beam lithography. [Pg.87]

Urethane-urea copolymer materials shown in Figure 16,12 are also promising for the application of near-field recording. " Figures 16.25a and... [Pg.533]

The vast majority of applications and theoretical treatments of ion exchange are concerned with the established copolymer materials previously described. However, an introduction to resin exchangers would be incomplete without a brief reference to some other more specialized products. [Pg.32]

Fig. 19.10 Inspection of the pH reagent immobilized in a cellulose acetate film and deposited onto a polycarbonate copolymer material upon immersion in solutions of low (a) and high (b) pH... Fig. 19.10 Inspection of the pH reagent immobilized in a cellulose acetate film and deposited onto a polycarbonate copolymer material upon immersion in solutions of low (a) and high (b) pH...
The solubility parameter concept has been used to correlate many physical phenomena. Miscibility of solvents with polymers, diffusion of solvents within polymers, effects of intermolecular forces on the glass transition temperature and interfacial interactions within copolymer materials would be included, just to mention a few examples. In many cases, meaningful interpretation of results was facilitated with the use of the solubility parameter. [Pg.67]

In the following sections, an overview of recent results regarding the synthesis by CRP of conjugated rod-coil suitable for flexible organic electronic systems, more specifically for photovoltaic devices, is presented. We will be particularly focusing on model semiconducting block copolymer materials and on small band gap copolymers. [Pg.245]

The accumulation of proteins on contact lenses has long been viewed as an undesirable event. In this study, the effect of polymer composition on both the total amount of protein on the materials, and on the specific proteins on each polymer composition was documented. The importance of these factors for biological response is not known, so this situation remains a fertile area for investigation. This study also demonstrated that a linear variation in material composition will not necessarily result in a linear variation in absorbed layer protein composition. The minima and maxima noted at intermediate copolymer compositions have strong implications for both understanding the mechanism of protein adsorption and for biological response. Investigation is underway to explore further protein interaction with hydrophobic-hydrophilic copolymer materials. [Pg.457]

IMPREGNATION OF SOFT SOUND WOOD WITH MONOMERS, which are then polymerized in situ by 7 radiation, was a method used in many laboratories during the 1960s in an effort to obtain wood-plastic composites. The process was attractive in two respects there was a large choice of consolidants, and radiation-induced polymerization had many advantages. Various vinyl monomers are cured by 7 rays. By proper selection of the polymer or copolymer, materials can be tailor made for specific applications. The radiation process presents several advantages over the chemically catalyzed polymerization of monomers in wood. [Pg.217]

The respective gel fraction of the irradiated CL-AGE copolymer materials was evaluated as follows. First, a 10 to 40 milligram sample of the irradiated CL-AGE copolymer free film was immersed and stirred in 200 ml of THF at room temperature for 72 hours. Then, the sample was removed from THF and dried in a vacuum oven at room temperature for 96 hours and the weight of the dried sample was measured. The gel content was given by the percent ratio of the final dried gel weight to the initial weight. [Pg.478]

Extensive and excellent literature [24, 25], can be found on block copolymers and their microphase separation. After a brief reminder of some necessary bases, we will focus here on the conditions allowing to access specific patterns at the free surface of a thin film. This concerns mostly really thin films, a regime in which the film structure will be strongly affected by its interfaces on the one hand, and by the commensurability of the film thickness T with a (small) integer number of d, the size of the microphase separation-induced period. This natural nanoscopic dimension constitutes a strong, almost inflexible constraint on the nanostructure of block copolymer materials, whatever their shaping, which will have specific consequences in the case of thin films. [Pg.74]


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See also in sourсe #XX -- [ Pg.281 ]




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