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Polycarbonate thermal

Thermal Properties. ABS is also used as a base polymer in high performance alloys. Most common are ABS—polycarbonate alloys which extend the property balance achievable with ABS to offer even higher impact strength and heat resistance (2). [Pg.203]

Polymerization by Transimidization Reaction. Exchange polymerization via equihbrium reactions is commonly practiced for the preparation of polyesters and polycarbonates. The two-step transimidization polymerization of polyimides was described in an early patent (65). The reaction of pyromellitic diimide with diamines in dipolar solvents resulted in poly(amic amide)s that were thermally converted to the polyimides. High molecular weight polyimides were obtained by employing a more reactive bisimide system (66). The intermediate poly(amic ethylcarboamide) was converted to the polyimide at 240°C. [Pg.403]

Minor and potential new uses include flue-gas desulfurization (44,45), silver-cleaning formulations (46), thermal-energy storage (47), cyanide antidote (48), cement additive (49), aluminum-etching solutions (50), removal of nitrogen dioxide from flue gas (51), concrete-set accelerator (52), stabilizer for acrylamide polymers (53), extreme pressure additives for lubricants (54), multiple-use heating pads (55), in soap and shampoo compositions (56), and as a flame retardant in polycarbonate compositions (57). Moreover, precious metals can be recovered from difficult ores using thiosulfates (58). Use of thiosulfates avoids the environmentally hazardous cyanides. [Pg.30]

A recently introduced polycarbonate-based blend offers a low coefficient of thermal expansion. This new thermoplastic is designed for large sheet applications such as doors or siding. Its high dimensional stability will eliminate warping from exposure to varying temperatures. [Pg.334]

Independently at the General Electric Company in America, work was being carried out in search of thermally and hydrolytically stable thermosetting resins. As a by-product from this work the research team at General Electric also produced polycarbonates from bis-phenol A so that by 1958 production of bis-phenol A polycarbonates was being carried out in both Germany and the USA. [Pg.557]

Typical figures for the basic thermal properties of polycarbonates are summarised in Table 20.5. [Pg.571]

Polycarbonates based on tetramethylbisphenol A are thermally stable and have a high Vicat softening point of 196°C. On the other hand they have lower impact and notched impact resistance than the normal polymer. Blends with styrene-based polymers were introduced in 1980, and compared with PC/ABS blends, are claimed to have improved hydrolytic resistance, lower density and higher heat deflection temperatures. Suggested applications are as dishes for microwave ovens and car headlamp reflectors. [Pg.579]

It has already been shown (e.g. Chapters 20 and 21) that the insertion of a p-phenylene into the main chain of a linear polymer increased the chain stiffness and raised the heat distortion temperature. In many instances it also improved the resistance to thermal degradation. One of the first polymers to exploit this concept commercially was poly(ethylene terephthalate) but it was developed more with the polycarbonates, polysulphone, poly(phenylene sulphides) and aromatic polyketones. [Pg.730]

Low smoke emission (roughly comparable to that of a polycarbonate). Very low coefficient of thermal expansion in the flow direction (0-15 cm/ cm/°C) but correspondingly higher in the transverse direction (27-76 cm/ cm/°C). [Pg.735]

Other topics recently studied by XPS include the effects of thermal treatment on the morphology and adhesion of the interface between Au and the polymer trimethylcy-clohexane-polycarbonate [2.72] the composition of the surfaces and interfaces of plasma-modified Cu-PTFE and Au-PTFE, and the surface structure and the improvement of adhesion [2.73] the influence of excimer laser irradiation of the polymer on the adhesion of metallic overlayers [2.74] and the behavior of the Co-rich binder phase of WC-Co hard metal and diamond deposition on it [2.75]. [Pg.28]

Hollomon s ethos, combined with his ferocious energy and determination, and his sustained determination to recruit only the best researchers to join his group, over the next 15 years led to a sequence of remarkable innovations related to materials, including man-made diamond, high-quality thermal insulation, a vacuum circuit-breaker, products based on etched particle tracks in irradiated solids, polycarbonate plastic and, particularly, the Lucalox alumina envelope for a metal-vapour lamp. (Of course many managers besides Hollomon were involved.) A brilliant, detailed account of these innovations and the arrangements that made them possible was later written by Guy Suits and his successor as director, Arthur Bueche (Suits and Bueche 1967). Some of these specific episodes will feature later in this book, but it helps to reinforce the points made here about Hollomon s coneeption of broad research on materials if I point out that the invention of translucent alumina tubes for lamps was... [Pg.9]

The occurrence of thermal failures in a plastic depends not only on the cyclic frequency and applied stress level but also on the thermal and damping characteristics of the material. For example, polycarbonate has very little... [Pg.141]

McNeill and Basan [151] studied the thermal degradation of blends of PVC with bisphenol-A polycarbonate. The structure of bisphenol-A polycarbonate is given in Eq. (42). [Pg.333]

The lower thermal stability of natural fibers, up to 230°C, the thermal stability is only small, which limits the number of thermoplastics to be considered as matrix materials for natural fiber composites. Only those thermoplastics whose processing temperature does not exceed 230°C are usable for natural fiber reinforced composites. These are, most of all, polyolefines, such as polyethylene and polypropylene. Technical thermoplastics, such as poyamides, polyesters, and polycarbonates, require... [Pg.803]


See other pages where Polycarbonate thermal is mentioned: [Pg.268]    [Pg.371]    [Pg.284]    [Pg.268]    [Pg.371]    [Pg.284]    [Pg.478]    [Pg.479]    [Pg.539]    [Pg.150]    [Pg.410]    [Pg.279]    [Pg.279]    [Pg.281]    [Pg.281]    [Pg.283]    [Pg.285]    [Pg.468]    [Pg.469]    [Pg.66]    [Pg.50]    [Pg.57]    [Pg.327]    [Pg.333]    [Pg.335]    [Pg.337]    [Pg.489]    [Pg.341]    [Pg.107]    [Pg.566]    [Pg.567]    [Pg.580]    [Pg.8]    [Pg.591]   


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Aliphatic polycarbonates thermal properties

Amorphous polycarbonate, thermal

Amorphous polycarbonate, thermal properties

Polycarbonate (thermally stabilized)

Polycarbonate Thermal expansion coefficient

Polycarbonate resin, thermal degradation

Polycarbonate thermal conductivity

Polycarbonate thermal diffusivity

Polycarbonate thermal properties

Polycarbonate, thermal decomposition

Polycarbonates thermal degradation

Polycarbonates thermal properties

R25 Polycarbonate (thermally stabilized)

Semicrystalline polycarbonate, thermal

Thermally depolymerizable polycarbonates

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