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Solvents quality parameter

The present review deals mainly with two examples of polyelectrolyte phase behavior as discussed above. As an example for an H-type precipitation, the solution properties of polyvinylpyridinium chains are monitored as function of added inert salt. Here, we focus on the determination of the effective charge density and of the solvent quality parameter which are supposed to play a central role for the understanding of polyelectrolyte solution without specific counterion interactions. The second system under investigation comprises the interaction of polyacrylic acid with alkaline earth cations which exhibit very specific interactions, thus representing an example for type L-precipitation. Here the coil dimensions close to the phase boundary are compared to those close to type H-precipitation with inert added salt. [Pg.32]

Qualitatively, the phase diagram fits very well to the phase diagram known for single-chain polyelectrolytes, the phase boundaries are only slightly shifted. In principle, the parameter space for polyelectrol ffes has far more dimensions, such as the solvent quality parameter, the valency of monomers or counterions, and additional salt concentration in the system. Especially for multivalent counterions, one can expect an even more complex picture, since correlation effects are known to play an important role even for single chains. [Pg.218]

Figure 2.6 Illustration of the effect of solvent quality parameter on chain geometry. Figure 2.6 Illustration of the effect of solvent quality parameter on chain geometry.
FIGURE 6.9 Dependence of viscoelastic parameters on solvent quality. The (A) static force, (B) drag coefficient at 10 kHz, (C) dynamic spring constant, and (D) dispersion parameter are shown as a function of the surface-sphere distance. The results for water, propanol, and a 50/50 water/propanol mixture are given. Reprinted with permission from Benmouna and Johannsmann (2004). [Pg.217]

At Merck KGaA in Darmstadt (Germany), in-line UV spectroscopy has been used for monitoring a distillation setup for solvent purification." A transmission probe was implemented at the top of the column. Solarization-resistant UV fibers guided the light to a diode array spectrometer. From the spectra, a quality parameter was extracted and fed to the process control system (PCS). As an example, the quality parameter would exhibit a transient behavior upon column startup. Below a defined threshold value of the parameter, the PCS would assume sufficient product quality and switch the exit stream from waste to product collection. The operation of the spectrometer does not take place in a direct manner, but rather via the PCS. [Pg.96]

The deterioration of the solvent qnality, that is, the weakening of the attractive interactions between the polymer segments and solvent molecules, brings about the reduction in the coil size down to the state when the interaction between polymer segments and solvent molecules is the same as the mutual interaction between the polymer segments. This situation is called the theta state. Under theta conditions, the Flory-Huggins parameter % assumes a value of 0.5, the virial coefficient A2 is 0, and exponent a in the viscosity law is 0.5. Further deterioration of solvent quality leads to the collapse of coiled structure of macromolecules, to their aggregation and eventually to their precipitation, the phase separation. [Pg.454]

Q Qo T V V0 Vf Vm x = Bn0m composition of solvent in the network Q = C>a/( a + b) composition of solvent outside the network Q0 = a/C a + < ) temperature expressed in energy units (i.e. kT) volume of the network sample volume of the network sample in the reference state total volume of system volume of micelles inside the network parameter characterizing solvent quality x > 0 corresponds to good solvent x < 0 to poor solvent x = 0 at 0-point... [Pg.126]

In addition to test kits used in EPA-approved screening methods, a variety of other test kits are available from several manufacturers, for example, immunoassay test kits for BTEX in soil and water and for chlorinated solvents in water colorimetric kits for the detection of lead kits for a wide range of water quality parameter manufactured by Hach Company. [Pg.175]

Fig. 42 Ratio R p/Rgi as a function of the interaction parameter x in a semi-logarithmic scale for the 127-unit alternating and protein-like chains in the corresponding multichain systems. The parameter x is similar to the Flory-Huggins interaction parameter X and characterizes solvent quality in an integral manner. Sufficiently large values of x (X > 1) correspond to a poor solvent. Solvent quality becomes poorer with decreasing temperature or with increasing x. Adapted from [212]... Fig. 42 Ratio R p/Rgi as a function of the interaction parameter x in a semi-logarithmic scale for the 127-unit alternating and protein-like chains in the corresponding multichain systems. The parameter x is similar to the Flory-Huggins interaction parameter X and characterizes solvent quality in an integral manner. Sufficiently large values of x (X > 1) correspond to a poor solvent. Solvent quality becomes poorer with decreasing temperature or with increasing x. Adapted from [212]...
Abstract Polyelectrolyte block copolymers form micelles and vesicles in aqueous solutions. Micelle formation and micellar structure depends on various parameters like block lengths, salt concentration, pH, and solvent quality. The synthesis and properties of more complicated block and micellar architectures such as triblock- and graft copolymers, Janus micelles, and core-shell cylinder brushes are reviewed as well. Investigations reveal details of the interactions of polyelectrolyte layers and electro-steric stabilization forces. [Pg.173]

An API is closely controlled in terms of crystal form, polymorph identity, particle size, impurity profile and content, solvent, and water levels. All of these quality parameters are defined in creating a drug product that has the desired pharmacological properties (e.g., tablet dissolution rate to give needed blood levels) and desired physical properties (e.g., stability and compatibility with drug delivery systems). [Pg.177]

Direct experimental data providing the temperature dependence of are not available in the literature. However, as discussed earlier, the dependence of 0 on the quality of the solvent (change in the values of the polymer-solvent interaction parameter) is expected to suggest the trend with temperature also. The experimental determination of

silica particles having polystyrene as the free polymer, indicated [5] that the amount of polymer required to produce phase separation decreased by a factor of three when the theta solvent cyclohexane (x = 0.5) is replaced by the good solvent toluene (x < 0.5). This implies that increased temperatures (reduced values for x) should lead to lower values of the amounts of polymer required for phase separation. It can be safely concluded that the available experimental and theoretical information thus far, exhibits the trend of smaller values of the limiting polymer concentration at higher temperatures. [Pg.239]

Official quality parameters comprise acidity, peroxide value, halogenated solvents, ultraviolet adsorption and sensory assessment. In addition to these official parameters important roles and high values are attributed to the content of the chlorophyll and carotene pigments and phenol antioxidants, as well as to the correlated induction time value. The significance of olive oil quality parameters is explained in Table 2.1. The phenol content and the related induction period, defined as the delay in the commencement of oxidation in an oil , merits particular comment the longer the induction period, the better the oil. Resistance... [Pg.33]

It is known that the coil-globule transition in flexible polymers is well explained by the theory of the type discussed [22]. Note that the chain length and the solvent quality come into the theory in the following combined form x = BN1/2/l3, which is the only dimensionless parameter governing the transition. The presence of the master curve (see Fig. 3.5 below) implies that the phase behavior of the thermodynamic limit with N —> oo is readily discussed from the measurement of shorter chains via finite-size scaling. [Pg.45]


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