Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

E system

In some cases, the temperature of the system may be larger than the critical temperature of one (or more) of the components, i.e., system temperature T may exceed T. . In that event, component i is a supercritical component, one that cannot exist as a pure liquid at temperature T. For this component, it is still possible to use symmetric normalization of the activity coefficient (y - 1 as x - 1) provided that some method of extrapolation is used to evaluate the standard-state fugacity which, in this case, is the fugacity of pure liquid i at system temperature T. For highly supercritical components (T Tj,.), such extrapolation is extremely arbitrary as a result, we have no assurance that when experimental data are reduced, the activity coefficient tends to obey the necessary boundary condition 1... [Pg.58]

Th c total en ergy of th e system. called the Hamilton iari, is ih c sum of th e kin elic an d poten tial energies (equation 24). [Pg.69]

Gamma/Phi Approach For many XT E systems of interest the pressure is low enough that a relatively simple equation of state, such as the two-term virial equation, is satisfactoiy for the vapor phase. Liquid-phase behavior, on the other hand, may be conveniently described by an equation for the excess Gibbs energy, from which activity coefficients are derived. The fugacity of species i in the liquid phase is then given by Eq. (4-102), written... [Pg.535]

Expansion Joints All the foregoing applies to stiff piping systems, i.e., systems without expansion joints (see detail 1 of Fig. 10-169). When space hmitations, process requirements, or other considerations result in configurations of insufficient flexibihty, capacity... [Pg.1001]

TOF detector systems usually have smaller solid angles and sensitivity than AF - E systems, because of the long TOF system in front of the energy detector and the limited size of the stop detector. They also have worse detection limits for very light elements (hydrogen), because of the low probability of obtaining start and stop signals for particles of very low atomic number [3.172]. [Pg.167]

CCF means different things to different people. Smith and Watson (1980) define CCF as the inability of multiple components to perform when needed to cause the loss of one or moi e systems. Virolainen (1984) criticizes some CCF analyses for including design errors and poor quality as CCF and points out that the phenomenological methods do not address physical and statistical dependencies. Here, CCF is classed as known deterministic coupling (KDC), known stochastic coupling (KSC), and unknown stochastic coupling (USC). [Pg.124]

K. V. Schubert, R. Strey. Small-angle neutron scattering from microemulsion near the disorder Une in water/formamide-octane-C,E systems. J Chem Phys 95 8532-8545, 1991. [Pg.740]

Volta potentials are measured by means of voltaic cells, i.e., systems composed of conducting, condensed phases in series, with a gas, liquid dielectric (e.g., decane) or a vacuum (in the case of solid conductors such as metals) gap situated between two condensed phases. The gap, g, may contain a gas such as pure air or nitrogen, saturated with vapors of the liquids present. Owing to the presence of a dielectric, special methods are necessary for the investigation of voltaic cells (see Section IV). [Pg.16]

The response of a controller to an error depends on its mode. In the proportional mode (P), the output signal is proportional to the detected error, e. Systems with proportional control often exhibit pronounced oscillations, and for sustained changes in load, the controlled variable attains a new equilibrium or steady-state position. The difference between this point and the set point is the offset. Proportional control always results in either an oscillatory behaviour or retains a constant offset error. [Pg.98]

O Heam. E. Battaglia, G. De Souza, E.B. Kuhar, M.J. and Molliver, M.E. Systemic MDA and MDMA, psychotropic substituted amphetamines, produce serotonin neurotoxicity. Abstr Soc Neurosci 12 1233, 1986. [Pg.302]

According to the patient s parameters what does he have (i.e., systemic inflammatory response syndrome, sepsis, or septic shock) ... [Pg.1190]

Moderately inferior to corresponding chlorine analog in this particular test. c Paralyzing effect decreased, but toxicity remained unchanged. d Exposure time 68 hours under same conditions 16% were affected by DDT. e Systemic poison, applied in soil supporting plants. [Pg.168]

Screening—to set priority (ranking) for detailed evaluation needs (based on building s location, type and use of the building, building age, A/M/E systems, etc). [Pg.57]

This argument, however, ignores an essential aspect of the second law, which is valid only for closed systems, i.e., systems for which neither matter nor energy can be exchanged with the environment. The chemical and physical processes which led to biogenesis on the primeval Earth did not take placed in closed systems, but in open ones. Matter and energy exchange were in fact essential for the successful execution of reaction sequences, as for example in the formation and synthesis of biomonomers. [Pg.239]

The objects of statistical mechanics however, are not single systems, but ensembles of many, say v, physically similar systems, i.e. systems with Hamiltonians H(qi,pi,t). The distribution of such a virtual ensemble over the phase space will be described by means of the density function q(qi,Pi, t), called the phase density. It is a real non-negative quantity and will always be normalized to unity, i.e. [Pg.436]

Rivas, J. M. and Ullrich, S. E., Systemic suppression of delayed-type hypersensitivity by supernatants from UV-irradiated keratinocytes. An essential role for keratinocyte-derived IL-10, J. Immunol 149, 3865-3871, 1992. [Pg.273]

Figure 1. A pH-pE diagram for the S-H20-H -e system at 298.15 K. The activities of the predominant sulphur compounds in solution are 101. Figure 1. A pH-pE diagram for the S-H20-H -e system at 298.15 K. The activities of the predominant sulphur compounds in solution are 101.
Figure 4. A pH-pE diagram for the Cu-Cl -H O-H -e system at 298.15 K. The activity of Cl is 101 the activities of the predominant copper solution species are 10 6. The diagram can represent only the most stable chloride complexes of cuprous and cupric and not the proportions of the various complexes. Figure 4. A pH-pE diagram for the Cu-Cl -H O-H -e system at 298.15 K. The activity of Cl is 101 the activities of the predominant copper solution species are 10 6. The diagram can represent only the most stable chloride complexes of cuprous and cupric and not the proportions of the various complexes.

See other pages where E system is mentioned: [Pg.29]    [Pg.45]    [Pg.76]    [Pg.96]    [Pg.97]    [Pg.159]    [Pg.159]    [Pg.218]    [Pg.268]    [Pg.316]    [Pg.268]    [Pg.230]    [Pg.727]    [Pg.167]    [Pg.188]    [Pg.2]    [Pg.100]    [Pg.1033]    [Pg.1459]    [Pg.23]    [Pg.14]    [Pg.62]    [Pg.122]    [Pg.693]   
See also in sourсe #XX -- [ Pg.136 ]




SEARCH



Addition of Cl- to the Ag E-pH System

Assay Systems and Models (e.g., Knock-out Mice)

Compounds of Aromatic Ring Systems E. O. Fischer and H. P. Fritz

Coupling ES Systems with Other Energy Devices

E Nonisothermal and Compositionally Nonuniform Systems

E,Z system

E,Z system of nomenclature

E. coli expression system

Electrical and other support systems (ES)

H*-e system

H20-H*-e system

Kimizuka, E. Takayama-Muromachi and K. Siratori, The systems

Naming Alkenes Using the E,Z System

Naming Stereoisomeric Alkenes by the E-Z Notational System

Q-e system

Skill 12.1o-Recognize that inorganic and organic compounds (e.g., water, salt, carbohydrates, lipids, proteins, nucleic acids) are essential to processes within living systems

Systems (e.g., H2O C2H6, C3H8, or i-C4Hio) with Upper Quadruple Points

The (E)-(Z) System for Designating Alkene Diastereomers

The Sulfuric Acid Solvent System R. J. Gillespie and E. A. Robinson

© 2024 chempedia.info