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Polycarbonate thermally stabilized

Peak Notation Assignment of Main Peaks Molecular Weight Retention Index Relative Intensity [Pg.268]


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]

Direct insertion probe pyrolysis mass spectrometry (DPMS) utilises a device for introducing a single sample of a solid or liquid, usually contained in a quartz or other non-reactive sample holder, into a mass spectrometer ion source. A direct insertion probe consists of a shaft having a sample holder at one end [70] the probe is inserted through a vacuum lock to place the sample holder near to the ion source of the mass spectrometer. The sample is vaporized by heat from the ion source or by heat from a separate heater that surrounds the sample holder. Sample molecules are evaporated into the ion source where they are then ionized as gas-phase molecules. In a recent study, Uyar et al. [74] used such a device for studying the thermal stability of coalesced polymers of polycarbonate, PMMA and polylvinyl acetate) (PVAc) [75] and their binary and ternary blends [74] obtained from their preparation as inclusion compounds in cyclodextrins. [Pg.426]

Three flame retardants were compared in this study, namely, a brominated polycarbonate oligomer (58% bromine), a brominated polystyrene (68% bromine), and a brominated triaryl phosphate ester (60% bromine plus 4% phosphorus). These are described in Table I. Figures 1 and 2 compare the thermal stability of the brominated phosphate with commercial bromine-containing flame retardants by thermogravimetric analysis (TGA) and by differential scanning calorimetry (DSC). The brominated phosphate melts at 110°C and shows a 1% weight loss at 300°C. Brominated polycarbonate and brominated polystyrene are polymeric and are not as volatile at elevated temperatures as the monomeric flame retardants. [Pg.255]

Requirements for CD-quality material are polycarbonate with low levels of chemical impurities, low particle levels, thermal stability, excellent mold release, excellent clarity, as well as constant flow and constant mechanical behavior (for reproducibility). There exists a time/cost balance. High molecular weight polycarbonate offers a little increase in physical property but the flow rate is slow, making rapid production of CDs difficult. The molecular weight where good mechanical strength and reasonable flow occurs, and that allows for short cycles, is in the range of 16,000-28,000 Da. [Pg.101]

Peng S, Dong L, Zhuang Y, Chen C (2001) Method for improving thermal stability of aliphatic polycarbonate using organic silanes, CN 1306022. CAN 137 34001... [Pg.45]

Yu T, Zhou Y, Liu K, Zhao Y, Chen E, Wang E, Wang D (2009) Improving thermal stability of biodegradable aliphatic polycarbonate by metal ion coordination. Polym Degrad Stab 94 253-258... [Pg.46]

Much attention has been paid to the synthesis of fluorine-containing condensation polymers because of their unique properties (43) and different classes of polymers including polyethers, polyesters, polycarbonates, polyamides, polyurethanes, polyimides, polybenzimidazoles, and epoxy prepolymers containing pendent or backbone-incorporated bis-trifluoromethyl groups have been developed. These polymers exhibit promise as film formers, gas separation membranes, seals, soluble polymers, coatings, adhesives, and in other high temperature applications (103,104). Such polymers show increased solubility, glass-transition temperature, flame resistance, thermal stability, oxidation and environmental stability, decreased color, crystallinity, dielectric constant, and water absorption. [Pg.539]

BPA polycarbonate becomes plastic at temperatures around 220°C, The viscosity decreases as the temperature increases, exhibiting Newtonian behavior, with the melt viscosity essentially independent of the shear rate, At the normal injection molding temperature of 270-3l5°C, the melt viscosity drops from 1.100 to 360 Pa j s (11.000 to 3,600 poise). Because the viscosity of polycarbonate can only be reduced by increasing the temperature, the ultimate limit on molecular weight is controlled by the processing conditions and the thermal stability of the polymer. [Pg.1336]

The lanthanides find some use as stabilizers for polymers. The coating of polycarbonate with a poly(vinyl alcohol) film containing CeCl3 inhibits photodegradation of the polycarbonate.151 The naphthenates of cerium, lanthanum and yttrium act as thermal stabilizers for polyorgano-siloxanes.152... [Pg.1027]

The degradation and combustion behavior of polycarbonate/POSS hybrid system has been reported recently.48 Different loading contents of trisilanolphenyl-POSS (TPOSS) were melt blended with polycarbonate matrix (PC). The data shown in Table 8.4 indicate that no improvement in thermal stability parameters (i.e., onset decomposition temperature and peak decomposition temperature) was observed compared to the neat polycarbonate. The thermo-oxidative degradation process of the hybrid system proved to be a complicated process, which includes hydrolysis/alcoholysis of the carbonate linkage, free radical oxidative chain degradation, reformation, and branching and cross-linking reactions. [Pg.197]

Ultramarine blues, reds and violets are acid sensitive. As such, their thermal and weathering properties are adversely affected in acidic media. Silica-encapsulated versions offer marked improvement in thermal stability and some improvement in weathering properties. The treated versions allow broad polymer usage, even in engineering plastics such as polycarbonate, and provide sufficient durability for automotive interior applications. Weatherability is highly dependent upon the degree of exposure to acid or alkaline conditions. [Pg.137]

Note-. 2 - sufficient thermal stability and limited reactivity with polymer allows broad use, 1 = marginal thermal stability or potential reactivity with polymer restricts use, 0 = generally unsuitable for use. FPVC, Flexible Polyvinyl Chloride RPVC, Rigid Polyvinyl Chloride PS, Polystyrene LDPE, Low Density Polyethylene HDPE, High Density Polyethylene PP, Polypropylene ABS, Acrylonitrile-butadiene-styrene copolymer PET, Polyethylene terephthalate PA, Polyamide PC, Polycarbonate... [Pg.142]

Applications for the Stabaxol stabilizers include thermoplastic polyester urethanes, polyesteramide thermoplastic elastomers, castable polyester urethanes, polyester polyols, monofilament PET fibers, polycarbonates, polycarbonate/PETblends, EVA copolymers and poly(caprolactones). The thermal stabilization of poly(ethylene sulfide) is also accomplished with 4 % hexamethylenebis(t-butyl)carbodiimide and 2 % diphenylacetylene. Also, alternating carbon monoxide/ethylene copolymers are stabilized using aromatic carbodiimides. ... [Pg.272]

The main advantage of polyimides is that they retain their structural strength to temperatures approaching 350 C, but they also have good outgassing characteristics in vacuum. For such applications the thermal stability of a PTFE filler is a limitation, and 5% of molybdenum disulphide may be added to a polyimide for friction reduction. The wear resistance of this material was inferior to some of the filled nylons, acetals and polycarbonates, and it would probably be chosen mainly for its high temperature stability. [Pg.222]

Glass and plastic vessels (but not nitrocellulose centrifuge pots) can be dried in an oven at the following temperatures, which depend on the thermal stability of the material polyvinyl chloride 70 °C polystyrene 70 °C polyethylene 80 °C high density polyethylene 120 °C polyallomer 130 °C polypropylene 130 °C polycarbonate 135 °C teflon 180 °C and glass 200 °C. [Pg.20]

Although polycarbonate is an engineering thermoplastic material which provides high toughness, flexibility and thermal stability, it suffers from certain limitations due to poor chemical resistance and low flow characteristics in injection moulding. These shortcomings can be circumvented by blending PC... [Pg.352]


See other pages where Polycarbonate thermally stabilized is mentioned: [Pg.268]    [Pg.371]    [Pg.268]    [Pg.371]    [Pg.479]    [Pg.591]    [Pg.324]    [Pg.810]    [Pg.11]    [Pg.865]    [Pg.317]    [Pg.322]    [Pg.241]    [Pg.253]    [Pg.264]    [Pg.541]    [Pg.458]    [Pg.210]    [Pg.18]    [Pg.25]    [Pg.279]    [Pg.279]    [Pg.281]    [Pg.281]    [Pg.469]    [Pg.1336]    [Pg.244]    [Pg.46]    [Pg.33]    [Pg.114]    [Pg.119]    [Pg.576]    [Pg.93]    [Pg.811]   


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Polycarbonate thermal

R25 Polycarbonate (thermally stabilized)

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