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Polydispersity mode

Under periodic operation, the polydispersity is greater by between 15-30% and the wave form of the forcing function has little effect. There is a small increase in both R and with respect to their steady-state values and the conversion appears to be little affected by the mode of operation of the reactor. [Pg.262]

The fracture strength and mode of fracture of a material have been found to be related to a number of characteristics of the polymer molecules of which it is made up. These include, among others, constitution, molar mass, polydispersity, crystallinity, and degree of crosslinking. Other factors which also affect fracture strength and mode of fracture are temperature, strain rate, and geometry of the specimen, all of which are decided upon prior to testing the material. [Pg.98]

The growing polymer chains have the most probable distribution defined by Equation (13.26). Typically, is large enough that PD 2 for the growing chains. It remains 2 when termination occurs by disproportionation. Example 13.5 shows that the polydispersity drops to 1.5 for termination by pure combination. The addition rules of Section 13.2.2 can be applied to determine 1.5 < PD < 2 for mixed-mode terminations, but disproportionation is the predominant form for commercial polymers. [Pg.484]

Few dispersions in everyday use are monodisperse and this will mean modification to Equation (3.54). A general expectation resulting from polydispersity is that denser packing may be achieved.22 The simplest case occurs for bi- or multimodal systems with very large size differences between each mode, several orders of magnitude for example. To calculate the zero shear viscosity of systems containing 1, 1 3, and... [Pg.85]

Fig. 12. The rheological functions G ((o) and G"(co) for an H-shaped PI of arm molecular weigh 20 kg mol and backbone 110 kg mol" [46]. The high-frequency arm-retraction modes can be seen as the shoulder from co 10 to co 10 together with a low-frequency peak due to the cross-bar dynamics at co 10. The smooth curves are the predictions of a model which takes Eq. (33) as the basis for the arm-retraction times and a Doi-Edwards reptation spectrum with fluctuations for the backbone. The reptation time is correctly predicted, as is the spectrum from the arm modes, though the low frequency form is more polydisperse than the simple theory predicts... Fig. 12. The rheological functions G ((o) and G"(co) for an H-shaped PI of arm molecular weigh 20 kg mol and backbone 110 kg mol" [46]. The high-frequency arm-retraction modes can be seen as the shoulder from co 10 to co 10 together with a low-frequency peak due to the cross-bar dynamics at co 10. The smooth curves are the predictions of a model which takes Eq. (33) as the basis for the arm-retraction times and a Doi-Edwards reptation spectrum with fluctuations for the backbone. The reptation time is correctly predicted, as is the spectrum from the arm modes, though the low frequency form is more polydisperse than the simple theory predicts...
Pileni MP, Motte L, Petit C (1992) Synthesis of Cadmiiun-Sulfide Insitu in Reverse Micelles - Influence of the Preparation Modes on Size, Polydispersity, and Photochemical Reactions. Chem Mater 4 338-345... [Pg.231]

If the signal can be expressed as a sum over exponentials, as in the case of solutions of polydisperse polymers, high-, low-, and band-pass filters which are exponentials in the time domain influence the amplitudes, but not the diffusion time constants of the respective modes [80,81]. [Pg.56]

Fig. 15 Variation of Kc with test speed in CT specimens of iPP with Mw of 455 kg mol 1 and a polydispersity of 5.4, tested in air, along with an indication of the mode of crack propagation [19]... Fig. 15 Variation of Kc with test speed in CT specimens of iPP with Mw of 455 kg mol 1 and a polydispersity of 5.4, tested in air, along with an indication of the mode of crack propagation [19]...
Fig. 21 The critical stress intensity for mode I crack initiation at different temperatures as a function of test speed in a iPP with Mw of 248 kg mol1 and a polydispersity of 5.2 and a similar material containing approximately 80 wt% y3 phase. The arrows mark ductile-brittle transitions in the y3 modified specimens [24]... Fig. 21 The critical stress intensity for mode I crack initiation at different temperatures as a function of test speed in a iPP with Mw of 248 kg mol1 and a polydispersity of 5.2 and a similar material containing approximately 80 wt% y3 phase. The arrows mark ductile-brittle transitions in the y3 modified specimens [24]...
The study that we describe below was inspired by our work on fitting the dynamic susceptibilities measurements for real assemblies of fine particles. Those data typically describe polydisperse systems in the low-frequency bandwidth a>/2% = 1 — 103 Hz. As To 10 s or smaller, then, using formula (4.132) for estimations, one concludes that the frequency interval mentioned becomes a dispersion range for the interwell (superparamagnetic) mode at coto< ct > 1, that is, a > 10. For temperatures up to 300 K, this condition holds for quite a number of nanomagnetic systems. [Pg.473]

Application of the two-mode models for a CSTR to the above kinetics results in a set of nonlinear algebraic equations, which when solved gives the MWD and the polydispersity index (PDI). For the case of premixed feed, Fig. 17 shows the variation of the MWD with n, where MWD is defined as... [Pg.272]

The transition between normal and steric-FFF mode depends on the particle size and lies for standard separation parameters at around 1 pm diameter (see Fig. 6). In this range, the elution behavior reverses, and the retention time is not any longer unique to a particle size. Consequently, the particle size determination of the size range can be erroneous, which can be a significant problem with polydisperse samples. However, most samples have sizes where the operation of one of the modes can be clearly assigned (see Fig. 6). The transition range between normal and steric-FFF mode has been considered in detail by Myers and Giddings [68]. [Pg.77]


See other pages where Polydispersity mode is mentioned: [Pg.194]    [Pg.228]    [Pg.194]    [Pg.228]    [Pg.296]    [Pg.218]    [Pg.260]    [Pg.62]    [Pg.61]    [Pg.145]    [Pg.426]    [Pg.15]    [Pg.227]    [Pg.215]    [Pg.229]    [Pg.295]    [Pg.38]    [Pg.294]    [Pg.21]    [Pg.181]    [Pg.291]    [Pg.109]    [Pg.307]    [Pg.517]    [Pg.236]    [Pg.233]    [Pg.293]   
See also in sourсe #XX -- [ Pg.194 ]




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Polydispersed

Polydispersion

Polydispersity

Polydispersiveness

Polydispersivity

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