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Laser light scattering solution

The molecular weight and its distribution have been determined by laser light scattering, employing a new apparatus for ETFE dissolution and solution clarification at high temperature diisobutyl adipate is the solvent at 240°C. The molecular weight of molten ETEE is determined by high temperature rheometry (21). [Pg.366]

Static (multi-angle laser) light scattering (SLS or MALLs) Molecular weight, radius of gyration, Rg solution conformation and flexibility. Solutions need to be clear of supramolecular aggregates. Rg more sensitive to conformation than s. [3]... [Pg.213]

Wu, C Laser Light Scattering Characterization of Special Intractable Macromolecules in Solution. Vol 137, pp. 103-134,... [Pg.216]

The concentration of the polymer molecules eluting from SEC columns is continuously monitored by a detector. The most widely used detector in SEC is the differential reftactometer (DRI), which measures the difference in refractive index between solvent and solute. Other detectors commonly used for SEC are functional group detectors ultraviolet (UV) and infrared (IR), and absolute molecular weight detectors low angle laser light scattering (LALLS) and in-line continuous viscometers. Applications of these detectors to SEC analysis will be discussed later in the Multiple Detectors Section. Other detectors also being used are the densimeter (11-19) and the mass detector (20-23). [Pg.5]

Chu, B., Zhou, Z., Wu, G., Farrell, Jr., H.M. (1995). Laser light scattering of model casein solutions effects of high temperature. Journal of Colloid and Interface Science, 170, 102-112. [Pg.221]

The solution behavior of poly(amic acids) was until recently, probably the least understood aspect of the soluble polyimide precursor. However, the advent of sophisticated laser light scattering and size exclusion chromatography instrumentation has allowed elucidation of the solution behavior of poly(amic adds). In the early days of polyimide chemistry, when most molecular weight characterization was based on viscosity determinations, a decrease in viscosity was associated with molecular weight degradation [15, 28, 29]. Upon combination of the two monomers an increase in the viscosity to the stoichiometric equivalence point is observed, followed by a decrease in the solution viscosity as a... [Pg.120]

The first data on polymer systems were collected via (laser-) light-scattering techniques [1] and turbidity measurements, further developed by Derham et al. [2,3]. Techniques based on the glass-transition of the polymer-blend constituents were also tested, such as DSC, Dynamic Mechanical Spectroscopy, and Dielectric relaxation [4]. Films made from solutions of... [Pg.576]

EOS models were derived for polymer blends that gave the first evidence of the severe pressure - dependence of the phase behaviour of such blends [41,42], First, experimental data under pressure were presented for the mixture of poly(ethyl acetate) and polyfvinylidene fluoride) [9], and later for in several other systems [27,43,44,45], However, the direction of the shift in cloud-point temperature with pressure proved to be system-dependent. In addition, the phase behaviour of mixtures containing random copolymers strongly depends on the exact chemical composition of both copolymers. In the production of reactor blends or copolymers a small variation of the reactor feed or process variables, such as temperature and pressure, may lead to demixing of the copolymer solution (or the blend) in the reactor. Fig. 9.7-1 shows some data collected in a laser-light-scattering autoclave on the blend PMMA/SAN [46],... [Pg.580]

Fig. 11. Low-angle-laser-light-scattering results of polyacrylamides in 0.1 M Na2S04-solution at 25 °C. Note at K c/Re = 0 the molecular weight should be Mw = oo definition... Fig. 11. Low-angle-laser-light-scattering results of polyacrylamides in 0.1 M Na2S04-solution at 25 °C. Note at K c/Re = 0 the molecular weight should be Mw = oo definition...

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See also in sourсe #XX -- [ Pg.115 ]




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