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Functions, excess standard

ACTIVITIES, EXCESS GIBBS FUNCTIONS, AND STANDARD STATES FOR NON ELECTROLYTES... [Pg.357]

From this equation, the temperature dependence of is known, and vice versa (21). The ideal-gas state at a pressure of 101.3 kPa (1 atm) is often regarded as a standard state, for which the heat capacities are denoted by CP and Real gases rarely depart significantly from ideaHty at near-ambient pressures (3) therefore, and usually represent good estimates of the heat capacities of real gases at low to moderate, eg, up to several hundred kPa, pressures. Otherwise thermodynamic excess functions are used to correct for deviations from ideal behavior when such situations occur (3). [Pg.235]

As is stated in the standard, all characteristics are important and need to be controlled. However, some need special attention as excessive variation may affect product safety, compliance with government regulations, fit, form, function, appearance, or the quality of subsequent operations. Designating such characteristics with special symbols alerts planners and operators to take particular care. It also alerts those responsible for dispo-sitioning nonconforming product to exercise due care when reaching their decisions. [Pg.366]

In the absence of simplifying assumptions a non-closed form analytical solution of these equations giving the concentration of each species as a function of time has been accomplished through the use of Bessel functions U1 ). Simplifying assumptions, such as a large hydroxyl excess, are acceptable theoretically but are not helpful in determining the rate constants of coatings materials with standard compositions. [Pg.243]

A simple and successful approximation for the excess free energy functional is to first assume that the excess free energy functional is only a functional of the average site density profile, denoted p(r), and then invoke standard approximations, similar to those used for simple liquids, for FEX- With a judicious choice of Fkx[Pm], the free energy functional can be exactly decomposed as... [Pg.123]

Under the Food Quality Protection Act (FQPA), the U.S. EPA evaluates the potential for people to be exposed to more than one pesticide at a time from a group of chemicals with an identified common mechanism of toxicity. As part of the examinations, to clarify whether some or all of the pyrethroids share a common mechanism of toxicity, a comparative FOB (functional observational battery) studies with 12 pyrethroids were carried out under standardized conditions [15]. The FOB was evaluated at peak effect time following oral administration of non-lethal doses of pyrethroids to rats using com oil as vehicle. Four principal components were observed in the FOB data [22], Two of these components described behaviors associated with CS syndrome (lower body temperature, excessive salivation, impaired mobility) and the others described behaviors associated with the T syndrome (elevated body temperature, tremor myoclonus). From the analysis, pyrethroids can be divided into two main groups (Type I T syndrome and Type II CS syndrome) and a third group (Mixed Type) that did not induce a clear typical response. Five other pyrethroids were also classified by an FOB study conducted in the same manner [16]. The results of these classifications are shown in Table 1. The FOB results for all non-cyano pyrethroids were classified as T syndrome, and the results of four ot-cyano pyrethroids were classified as CS syndrome however, three of the ot-cyano pyrethroids, esfenvalerate, cyphenothrin, and fenpropathrin, were classified as Mixed Type. [Pg.86]

Figure 16 is a graph of Zn and Se coverages per cycle for ZnSe deposits as a function of the Zn potential. The Se deposition was carried out by first depositing two monolayers at -0.9 V and then reducing off the excess at -0.9 V. The drop in coverage above -0.8 V is due to decreased stability of the Zn (Fig. 11). A plateau in both the Zn and Se coverages is evident between -1.2 and -0.9 V, however, the Zn coverage per cycle is nearly 3/4 ML, while the Se remains at 1/2 ML. The standard potential for Zn deposition is about -1.0 V (vs. Ag/AgCl), and given that a mM solution of ZnS04 was used, bulk deposition would not be expected until -1.1 V. The reason for the disparity between the Zn and Se in the... Figure 16 is a graph of Zn and Se coverages per cycle for ZnSe deposits as a function of the Zn potential. The Se deposition was carried out by first depositing two monolayers at -0.9 V and then reducing off the excess at -0.9 V. The drop in coverage above -0.8 V is due to decreased stability of the Zn (Fig. 11). A plateau in both the Zn and Se coverages is evident between -1.2 and -0.9 V, however, the Zn coverage per cycle is nearly 3/4 ML, while the Se remains at 1/2 ML. The standard potential for Zn deposition is about -1.0 V (vs. Ag/AgCl), and given that a mM solution of ZnS04 was used, bulk deposition would not be expected until -1.1 V. The reason for the disparity between the Zn and Se in the...

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See also in sourсe #XX -- [ Pg.86 ]




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