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Thermal equilibrimn

In Sect. 4.2.7 it will be shown that the emission of the backgroimd decays also at T = 1.3 K biexponentiaUy with time constants of 600 ns and 110 ps. This is due to the fact that both states I and II are not in a fast thermal equilibrimn. By time-resolved emission spectroscopy one can separate the super-imposed emissions of the two states. Details are discussed in Sect. 4.2.8. [Pg.135]

These normal modes evolve independently of each other. Their classical equations of motion are Uk = —co Uk, whose general solution is given by Eqs (6.81). This bath is assumed to remain in thermal equilibrimn at all times, implying the phase space probability distribution (6.77), the thermal averages (6.78), and equilibrium time correlation functions such as (6.82). The quantum analogs of these relationships were discussed in Section 6.5.3. [Pg.458]

We will consider a process in which the external field is switched on at the distant past, when the system was at thermal equilibrimn, p(tp — oo) = pec = exp(—)6. M)/Tr exp(—Referring to this initial time, Eq. (18.79) represents the deviation from thermal equilibrium caused by the external field, written as a sum of terms of increasing orders in this field... [Pg.694]

Prom chemical point of view, what these motor proteins do is they catalyze the reaction of hydrolysis of ATP each act of hydrolysis yields energy about 14 ksT. Motor proteins use this energy to perform directed walk in one particular chosen direction (instead of random walk in random direction in thermal equilibrimn). [Pg.79]

There are very well established natural laws, ealled the laws of thermodynamies, working behind the scenes. Along with a few other features, these laws state that objects in contact with each other, absent arty external heating or cooling, will reach a state called thermal equilibrium, in whieh their temperatures will be eqtral. Under normal kitchen conditions, half an hoirr is more than errough to reach this thermal equilibrimn, so all objects in contact with air will have identical temperatiues. Why then, do they feel so different ... [Pg.268]

In thermal equilibrimn the partition of the total energy into the different modes is governed by the Maxwell-Boltzmann distribution, so that the probability p q) that a mode contains the eneigy qhv is... [Pg.9]

In Sect. 2.1 it was shown that in a closed cavity a radiation field exists with a spectral energy density p v) that is determined by the temperature T of the cavity walls and by the eigenfrequencies of the cavity modes. In the optical region, where the wavelength X is small compared with the dimension L of the cavity, we obtained the Planck distribution (2.13) at thermal equilibrimn for p(v). The number of modes per imit volume,... [Pg.241]

A non-thermal, non-equilibrium plasma is characterized by an electron temperature much larger than the ion temperature Jj and the neutral gas temperature T T. Typical non-thermal, non-equilibrimn plasmas... [Pg.2796]

The higher conversion of methanol synthesis was obtained by applying more effective heat removal to keep reaction temperature as low as possible [17]. The removal of methanol product during the reaction also shifts the equilibrimn to higher conversion. Consequently, the higher total carbon conversion in SC-Ce can be illustrated in terms of both more effective heat transfer and high molecular diffusion efficiency. The more effective heat transfer resulted from the higher thermal conductivity of the SC phase which... [Pg.374]

The environment is a large equilibrimn system in which the state variables (To, po) and the chemical potential of the chemical components contained in it remain constant, when, in a thermodynamic process, heat and materials are exchanged between another system and the environment. It is important that no chemical reactions can take place between the environmental chemical components. The environment is free of irreversibilities, and the exergy of the environment is equal to zero. The enviromnent is part of the surroimdings of any thermal system. [Pg.248]

The statistical mechanics of systems not in thermal equilibrium. One of the main purposes ot non-equilibrium statistical mechanics is to calculate transport coelSclents and inverse transport coefficients, such as conductivity and viscosity, from first principles and to provide a basis tor transport theory. The non-equilibrium systems easiest to understand are those near thermal equilibrium. For systems tar from equilibrimn, such possibilities as chaos, turbulence, and selforganization can arise due to nonlinearity. [Pg.565]

When the adsorption temperature is increased to 373 K and then to 473 K, there is a decrease in the time required to establish equilibrium and a decrease in the region of coverage in which slow adsorption is observed [29]. At 573 K and 673 K, equilibrimn is established rapidly at all coverages. The time to establish thermal equilibrium in this case is determined solely by the inertia of the calorimeter. When using probes, the molecular diameter of which is much larger than that of NH3, other diffusional problems also occur. [Pg.53]


See other pages where Thermal equilibrimn is mentioned: [Pg.287]    [Pg.66]    [Pg.287]    [Pg.66]    [Pg.167]    [Pg.213]    [Pg.338]    [Pg.422]    [Pg.253]    [Pg.349]    [Pg.330]    [Pg.37]    [Pg.384]    [Pg.180]    [Pg.281]    [Pg.282]    [Pg.180]   
See also in sourсe #XX -- [ Pg.12 ]




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