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Temperature thermal degradation

Polymer T,°C TJC Softening temperature,°C Thermal degradation temperature,°C... [Pg.314]

The porous electrodes in PEFCs are bonded to the surface of the ion-exchange membranes which are 0.12- to 0.25-mm thick by pressure and at a temperature usually between the glass-transition temperature and the thermal degradation temperature of the membrane. These conditions provide the necessary environment to produce an intimate contact between the electrocatalyst and the membrane surface. The early PEFCs contained Nafton membranes and about 4 mg/cm of Pt black in both the cathode and anode. Such electrode/membrane combinations, using the appropriate current coUectors and supporting stmcture in PEFCs and water electrolysis ceUs, are capable of operating at pressures up to 20.7 MPa (3000 psi), differential pressures up to 3.5 MPa (500 psi), and current densities of 2000 m A/cm. ... [Pg.578]

Methylene chloride is one of the more stable of the chlorinated hydrocarbon solvents. Its initial thermal degradation temperature is 120°C in dry air (1). This temperature decreases as the moisture content increases. The reaction produces mainly HCl with trace amounts of phosgene. Decomposition under these conditions can be inhibited by the addition of small quantities (0.0001—1.0%) of phenoHc compounds, eg, phenol, hydroquinone, -cresol, resorcinol, thymol, and 1-naphthol (2). Stabilization may also be effected by the addition of small amounts of amines (3) or a mixture of nitromethane and 1,4-dioxane. The latter diminishes attack on aluminum and inhibits kon-catalyzed reactions of methylene chloride (4). The addition of small amounts of epoxides can also inhibit aluminum reactions catalyzed by iron (5). On prolonged contact with water, methylene chloride hydrolyzes very slowly, forming HCl as the primary product. On prolonged heating with water in a sealed vessel at 140—170°C, methylene chloride yields formaldehyde and hydrochloric acid as shown by the following equation (6). [Pg.519]

Fig. 11. Thermal degradation temperature of standard PHB and PHB obtained from Bacillus aryahhattai by Thermo-gravimetric analysis (TGA)... Fig. 11. Thermal degradation temperature of standard PHB and PHB obtained from Bacillus aryahhattai by Thermo-gravimetric analysis (TGA)...
While physicochemical and spectroscopic techniques elucidate valuable physical and structural information, thermal analysis techniques offer an additional approach to characterize NOM with respect to thermal stability, thermal transitions, and even interactions with solvents. Information such as thermal degradation temperature (or peak temperature), glass transition temperature, heat capacity, thermal expansion coefficient, and enthalpy can be readily obtained from thermal analysis these properties, when correlated with structural information, may serve to provide additional insights into NOM s environmental reactivity. [Pg.785]

Specific heat (J/(kg K)d Thermal degradation temperature, °C Low temperature embrittlement, °C Water absorption, %... [Pg.47]

ILs are defined as organic salts having a melting point (Tm) below 100°C [1-5]. In order to use these ILs as non-volatile electrolyte solutions, it is necessary to maintain the liquid phase over a wide temperature range. Consequently, Tm and the thermal degradation temperature (Tfj of ILs are important properties for ILs as electrochemical media. In this section, the thermal properties of ILs, especially of imidazolium salts, are summarized. The difference between ILs and general electrolyte solutions based on molecular solvents is clarified. Recent results on the correlation between the structure and properties of ILs will also be mentioned. [Pg.47]

It is known [1], that the intensive thermal degradation temperature Td characterizes the polymer s thermostability. As the characteristic of thermostability according to [2] limiting temperature is accepted at which chemical change of polymer reflected on its properties takes place. The thermostability is determined with the aid of thermogravimetric analysis (TGA). Hereafter under Td a sample of 5%-th mass loss temperature obtained in TGA testing will be understand. [Pg.73]

Figure 3 shows a thermogravimetric analysis performed on the two molding compounds. The scans show that the molding compound based on the stable bromine CEN has a 15-20°C increase in thermal degradation temperature over the standard compound. Even though the stable bromine CEN is more thermally stable than standard resins, it still supplies the bromine necessary to achieve the desired flame retardancy properties. [Pg.402]

Another mechanism for the formation of acids is through thermal degradation. There is no easy solution to this problem, so the operational temperatures of the commercial aircraft hydraulic systems must be maintained well below the thermal degradation temperatures of the phosphate ester hydraulic fluids, reported as being above 200°C [26]. [Pg.367]

The catalysts can also be bonded onto each face of the membrane under pressure and at a temperature (22) usually between the glass transition temperature and the thermal degradation temperature of the membrane (17,23,24). At such temperatures the membrane softens and can flow under pressure, such that the adhesion force of the membrane is at a maximum, and an intimate contact between the catalyst and the membrane can be achieved (17). The heating process is rather short, so that the membrane is not over-dehydrated. A dehydrated membrane gives poor bonding (17). [Pg.451]

The physical properties of the polymer often dictate the spinning method that must be used for fiber formation. For example, if the melt temperature is above the thermal degradation temperature, the polymers cannot be melt spun. Such polymers must be liquified with... [Pg.457]

A low shear heat screw is recommended, with L/D = 18 to 22 and a compression ratio from 2.0 to 2.6. The screw should be protected against corrosion and wear, by either plating or nitrating. If any scratch is observed on the surface of the barrel, screw, or nozzle, it must be repaired immediately, otherwise owing to resin retention, it may cause burn marks or black spots on the moldings. The resin temperature may be checked with a few air shots. Due to thermal degradation, temperatures above 210°C may cause burn marks, black spots or mold-rust. [Pg.713]

Polyphenylene ether resins were developed in the early 60 s but could not be processed because the thermal degradation temperature was a few degrees below the melt temperature required for processing. Later discovery that PS can act as a plasticizer lead to the introduction of PPE/PS, one of the most successful blend (Noryl , Prevex , Luranyl ). [Pg.723]

In semicrystalline polymers, such as chitin and CS, the value of the glass transition temperature characteristic of the amorphous material was controversial even as to whether polysaccharides exhibit a glass transition temperature (Eg). For many natural polymers, Eg is above the thermal degradation temperature [10]. For chitin, some authors have not observed a glass transition [11], while others report an apparent a-relaxation at 236 °C for a-chitin [12] and 170 °C for P-chitin [13] using DMTA measurements. Lee et al. [14] report an apparent a-relaxation at 182 °C for 3-chitin by dielectric measurements. [Pg.16]

Thermal Stability and Conductivity. Thermal degradation temperature of PMMA, PS, and PVA (poly(vinyl alcohol)) nanocomposites shifts up by 10-100°C. During combustion [179], nanoparticles form a network of char layers that retards the transport of decomposition products. The thermal conductivity of epoxy composites is four times higher than that of the neat epoxy resin with 5 wt% loads. [Pg.599]

This method is applicable to blends containing polymers with significantly different thermal degradation temperatures. It has been used for analysis of carbon black distribution in NR-SBR and NR-BR blends (Hess et al 1985a Hess and Chirico, 1977). [Pg.576]


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See also in sourсe #XX -- [ Pg.47 ]

See also in sourсe #XX -- [ Pg.105 , Pg.107 , Pg.108 , Pg.112 , Pg.113 ]




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