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Primary phase separation

Let us briefly review the primary treatment methods used. Pretreatment usually starts with phase separation if the effluent is a heterogeneous mixture. [Pg.310]

Polymer alloys are generally named polymer blends within the polymer community. In a recent overview of such blends, Robeson (1994) points out that the primary reason for the surge of academic and industrial interest in polymer blends is directly related to their potential for meeting end-use requirements . He points out that, in general, miscible polymer pairs confer better properties, mechanical ones in particular, than do phase-separated pairs. For instance, the first commercial... [Pg.326]

The application of this procedure is best seen by performing an FMEA on a simple two-phase separator. Table 14-3 lists those process upsets that can be sensed before an undesirable event leading to a source of condition occurs. For overpressure, primary protection is provided by a high pressure sensor that shuts in the inlet (PSH). If this device fails, secondary protection is provided by a relief valve (PSV). [Pg.400]

The separation of mixtures involving N-methyl-JLtetrahydropyridines into their pure components by means of gas-liquid chromatography was discussed in a report by Holik et al. (87). They found that, using tris(/3-cyanoethoxymethyl)-y-picoline as the stationary phase, the primary factors involved in the specific retention volumes of these enamines is the electronic effect of a methyl substituent and the nitrogen atom on the carbon-carbon double bond. It was observed that 1,3-dimethyl-Zl -tetrahydropyridine (141) has a smaller specific retention volume and, hence, is eluted before... [Pg.50]

In the case of the higher temperature crystallization, as will be shown in Sect. 4, the theory of Doi et al. is applicable without doubt since the primary phase separation involves the transition from the isotropic to nematic phase, but in the case of the glass crystallization near Tg described above its applicability is unclear since the observed data may correspond to the secondary phase separation. However, if the secondary phase separation occurs, the primary phase separation must have proceeded prior to that. In a rapidly quenched glass even if the primary phase separation had already taken place, it would be still incomplete, so that it will re-start by heating. [Pg.203]

Fig. 25 Annealing time evolution of the difference SAXS intensity in the induction period (a) and the crystallization period (b) for the melt crystallization of PET at 244 °C [18]. This system corresponds to crystallization from the metastable state where a nucle-ation and growth type of primary phase separation first occurs followed by the spinodal decomposition type secondary phase separation... Fig. 25 Annealing time evolution of the difference SAXS intensity in the induction period (a) and the crystallization period (b) for the melt crystallization of PET at 244 °C [18]. This system corresponds to crystallization from the metastable state where a nucle-ation and growth type of primary phase separation first occurs followed by the spinodal decomposition type secondary phase separation...
Conformational and phase transitions can potentially be indicative of the primary structure of thermosensitive macromolecules. Indeed, depending on the relative location of H- and P-blocks, as well as on the variation of their length, the chains can either undergo conformational transition accompanied by phase separation, or they can exhibit only the conformational changes without macroscopic phase transitions, i.e. the behaviour observed in the case of protein-like HP-copolymers. Therefore, the solution behaviour of separated fractions of these NVCl/NVIAz-copolymers in an aqueous medium at different temperatures is very important. [Pg.115]

In the primary structure of alternating block-copolymers the hydrophobic H-type blocks could be too short to facilitate the efficient cooperative hydrophobic interactions responsible for promoting the phase separation. [Pg.117]

PVA and TaM -for the 88%-hydrolyzed PVA. The same dependence was found for the adsorbed layer thickness measured by viscosity and photon correlation spectroscopy. Extension of the adsorption isotherms to higher concentrations gave a second rise in surface concentration, which was attributed to multilayer adsorption and incipient phase separation at the interface. The latex particle size had no effect on the adsorption density however, the thickness of the adsorbed layer increased with increasing particle size, which was attributed to changes in the configuration of the adsorbed polymer molecules. The electrolyte stability of the bare and PVA-covered particles showed that the bare particles coagulated in the primary minimum and the PVA-covered particles flocculated in the secondary minimum and the larger particles were less stable than the smaller particles. [Pg.77]

A similar reaction has been conducted under fluorous biphasic conditions, using a perfluoroalkylated bipyridine as ligand to ensure that the copper species resides in the fluorous phase [22], The oxidation of a range of primary alcohols to the corresponding aldehydes was found to be possible, an example of which is shown in Scheme 9.11. The catalyst could be successfully recycled by phase separation, with analytically pure products being isolated even after... [Pg.188]


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See also in sourсe #XX -- [ Pg.127 ]




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