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Loss mechanisms transition

Both 1st- and 2nd-order rate expressions gave statistically good fits for the control samples, while the treated samples were statistically best analyzed by 2nd-order kinetics. The rate constants, lst-order activation parameters, and char/residue yields for the untreated samples were related to cellulose crystallinity. In addition, AS+ values for the control samples suggested that the pyrolytic reaction proceeds through an ordered transition state. The mass loss rates and activation parameters for the phosphoric acid-treated samples implied that the mass loss mechanism was different from that for the control untreated samples. The higher rates of mass loss and... [Pg.335]

A further possibility is that molecules undergo a nonradiative transition from the excited singlet states to the triplet states (intersystem crossing). This is the origin of some loss mechanisms for dye lasers. [Pg.57]

The y Relaxation. In common with many other polymers (8) both PPO and PS display significant loss maxima below room temperature at the frequencies under consideration. Whereas the process responsible for the a loss is at least qualitatively understood in terms of a main chain relaxation associated with the glass transition, y losses can often only tentatively be attributed to specific mechanisms. In PPO, for example, it does not seem unreasonable to propose that the y loss is associated with librations in the two pendant methyl groups this view is somewhat reinforced by the observation that in the dielectric measurements the relaxational strengths of the y and a loss processes are comparable. As the latter can be well interpreted (6) in terms of a dipolar relaxation of the main chain in which the entire dipolar contributions arise from the methyl groupings, it seems plausible to assume that the same dipoles are responsible for the y loss mechanism. In polystyrene there is a similar... [Pg.49]

Analysis of the ft transition of MT copolyamides (described in [1], Sect. 5) shows that in the mechanical loss ft transition of MT Ii copolyamides, in the low-temperature range part of the involved motions are those of CH2 units. At higher temperatures phenyl ring motions (oscillations then jr-flips), coupled with amide group motions, occur. [Pg.349]

The light output of a LED is given by the injection current and the radiative efficiency and is governed by two primary loss mechanisms. A large fraction of the recombination at room temperature is by non-radiative transitions at defects (see Section 8.3.5). The thermal quenching of the photoluminescence is lower in the alloys than in... [Pg.379]

Transition from the Initial dry to subsequent wet environment caused an Initial Increase In the tan 5 and loss mechanical properties for the sample as shown In Figure 5. This behavior may be explained In terms of a plasticizing effect. [Pg.103]

The apparent activation energies ( ACT) of the dynamic mechanical transitions can be calculated from the temperature at the maximum in the loss modulus T(G"max) as a function of frequency. A typical Arrhenius plot (see Fig. 2) of the apparent activation energy of the soft segment glass transition for 73 series polymers yields E/ ct values of approximately 75 + 5 kcal/mole (314 kJ/mole) over a frequency range of 2 decades. [Pg.347]

Dynamic mechanical transition temperatures were measured at the maximum in the loss modulus at 0.1 Hz. [Pg.352]

REELS provides information concerning higher energy loss mechanisms than HREELS such as plasmons, interband transitions and characteristic energy losses. EXELES is a technique used in TEM (transmission electron microscopes). It provides information similar to EXAFS (X-ray absorption fine structure), (i.e. data regarding the immediate neighbourhood of atoms of certain elements in the sample). EXELES is bulk sensitive. [Pg.535]


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Mechanical loss

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