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Plastic matrices

Halogenated Epoxy Matrix Plastics in Filament-Wound Composites... [Pg.481]

Figure 1. Water absorption of bulk matrix plastics containing chlorine... Figure 1. Water absorption of bulk matrix plastics containing chlorine...
Competition between matrix plasticity and grain boundary/interfacial separation due to the flow of the glass phase. [Pg.228]

Our study is outlined in five parts, (a) Two polystyrene plastics were reinforced at different fiber contents alternately with polyester, asbestos, and glass fibers, (b) The mechanical/physical properties of the resultant monofiber-reinforced plastics were determined and compared, (c) Combinations of fibers were then used to fabricate multifiber-rein-forced structures to exploit simultaneously the particular advantages of the different reinforcements, (d) The effect of each fabrication stage on the molecular weight and molecular weight distribution of the matrix plastics was established and (e) a linear mathematical model was formulated to predict the properties of multifiber structures and forecasted values compared with corresponding values experimentally obtained from (c) above. [Pg.387]

Matrix Plastic Foams. The matrix for plastic foams includes rigid polyurethane foam, urethane-modified isocyanurate foam, unsaturated polyester-polyurethane hybrid foam, and vinyl ester-polyurethane hybrid foam. [Pg.164]

In the photorefractive polymer composites described above, the value of the glass transition temperature is of great importance because it needs to be in a range where the electro-active chromophores can be reoriented by the photorefractive space-charge charge field. Adjustment of Tg is done though the addition of a plasticizer. Examples of plasticizers are shown in Fig. 23. As for the polymer matrixes, plasticizers can be photoconducting or inert. ECZ (molecule (a) in Fig. 23) is widely used with PVK. Inert plasticizers such as BBP (molecule (c) in Fig. 23) have also been combined with PVK [86]. [Pg.145]

Regardless of the mechanism, the results most clearly illustrate that a alone does not provide an adequate mechanism to explain the role of moisture in governing food stability. Model systems are perfect for studying the complexities of reactant mobility as a determinant for reaction rate. What is lacking is a study that examines multiple aspects of mobility in correlation to the rate of a chemical reaction. Changes in moisture content and affect matrix plasticity and thus mobility, solute solvency, rotational mobility, and translational mobility. Each of these aspects of mobility may or may not each have an effect on reaction rate, depending on the reaction and the chemical constituents within the system. [Pg.361]

Other variables investigated with respect to fracture toughness include processing parameters, e.g.. production schedules and postcure cycles [166.171] for thermosets, and cooling rates for thermoplastics [171] matrix composites, and moisture content. A study [171] on composites based on epoxy and vinyl ester matrices has shown that whilst matrix plasticization improves mode I fracture toughness, mode II fracture toughnc.ss deteriorates due to interface degradation. The sensitivity of (Jut to water absorption has been demonstrated even for matrices that absorb very small amounts of water such as pol propy lene [168]. [Pg.571]

A tool for ultra-high-density optical memory and a fruitful spectroscopic method of detecting properties of matrix plastics. Various kinds of materials have been used for establishing the relationship between PHB phenomena and properties of materials. As an example, dye molecules in amorphous plastic systems have been used because of their high-quantum yield and good processability. See amorphous plastic. [Pg.404]

A significant development is a technique for pulping or fibrillation that greatly increases the surface area of short-length fibers of para-aramid, and renders them suitable for reinforcement of plastics and elastomers. A typical staple fiber will have a surface area of about 0.1 m /g, but the compounding process increases this to 7-9 mVg, so increasing the area available for adhesion to the matrix plastic. The bond achieved will... [Pg.68]

The gradual growth of the total USA plastic [RP and URP (unreinforced plastic)] industry for over a century has been spectacular evolving into today s routine to sophisticated high performance products (parts). Examples of these products are in building and construction (34 wt%), transportation (33%), sports and appliances (14%), electrical and electronic (10%), and others (9%). Use is made of thermoplastic (TP) and thermoset (TS) plastic matrixes. Plastics data source, such as the Society of Plastics Industry s (SPI s) suite of economic studies and statistics, provide current, comprehensive data, and analysis of the domestic and international trade markets for USA plastic materials, processing, machinery, and moldmaking industries that follows the ups and downs of the overall local and worldwide economy (www.plasticsdatasource.org or tel. 800.541.0736). [Pg.483]

Similarly, there are three primary classes of polymer materials usually referred to in the general class of plastics by consumers and industry. Their design is often that of a composite, where a polymer matrix (plastic material) forms a dominant phase around a filler material. The filler is present in order to increase mechanical properties, and decrease material costs. [Pg.187]

The oxygen diffusion coefficient as a function of water activity for 98L-PLA is presented in Fig. 3a. An exponential increase of the oxygen diffusion coefficients from 2 X 10 " to 9 X 10 " m /s at 23°C can be observed as water activity increased from 0 to 0.9. The observed increase of the oxygen diffusion coefficient in the range of = 0-0.9 can be attributed to the plasticization effect on the amorphous phase by the water molecules. Plasticization effects tend to increase the mobility of the oxygen molecules in the polymer matrix. Plasticization effects are evidenced by a reduction of the polymer s 7 g [43]. [Pg.355]

Plasticity The ability to deform plastically. Ability to irreversibly deform under an applied stress by motion within the tape matrix. Plastic deformation causes rearrangement within the tape structure, and thus the tape does not revert to its original shape when the applied stress is removed. [Pg.272]


See other pages where Plastic matrices is mentioned: [Pg.103]    [Pg.241]    [Pg.241]    [Pg.104]    [Pg.481]    [Pg.53]    [Pg.201]    [Pg.477]    [Pg.42]    [Pg.43]    [Pg.35]    [Pg.514]    [Pg.514]    [Pg.559]    [Pg.775]    [Pg.424]    [Pg.20]    [Pg.29]    [Pg.191]    [Pg.192]    [Pg.142]    [Pg.146]    [Pg.36]    [Pg.462]    [Pg.207]    [Pg.12]    [Pg.20]    [Pg.29]    [Pg.191]    [Pg.192]    [Pg.84]    [Pg.3451]   
See also in sourсe #XX -- [ Pg.265 ]




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