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State space defined

We will use Cartesian sums and tensor products to build and decompose representations in Chapters 5 and 7. Tensor products are useful in combining different aspects of one particle. For instance, when we consider both the mobile and the spin properties of an electron (in Section 11.4) the state space is the tensor product of the mobile state space defined in Chapter 3)... [Pg.70]

The polyad model for acetylene is an example of a hybrid scheme, combining ball-and-spring motion in a two-dimensional configuration space [the two Franck-Condon active modes, the C-C stretch (Q2) and the tram-bend (Q4)] with abstract motion in a state space defined by the three approximate constants of motion (the polyad quantum numbers). This state space is four dimensional the three polyad quantum numbers reduce the accessible dimensionality of state space from the seven internal vibrational degrees of freedom of a linear four-atom molecule to 7 - 3 = 4. [Pg.595]

We consider a two state system, state A and state B. A state is defined as a domain in phase space that is (at least) in local equilibrium since thermodynamic variables are assigned to it. We assume that A or B are described by a local canonical ensemble. There are no dark or hidden states and the probability of the system to be in either A or in B is one. A phenomenological rate equation that describes the transitions between A and B is... [Pg.276]

More abstractly the condition Tr (p+p ) = iV implies that the part of the Hilbert space defined by the projection operator p should be fully contained in the part defined by the projection operator p+. If we now vary p slightly so that this condition is no longer fulfilled, Eq. II.GO shows that the pure spin state previously described by the Slater determinant becomes mixed up with states of higher quantum numbers S = m+1,. . . . The idea of the electron pairing in doubly occupied orbitals is therefore essential in the Hartree-Fock scheme in order to secure that the Slater determinant really represents a pure spin state. This means, however, that, in the calculation of the best spin orbitals y>k(x), there is a new auxiliary condition of the form... [Pg.231]

The wave function is an irreducible entity completely defined by the Schrbdinger equation and this should be the cote of the message conveyed to students. It is not useful to introduce any hidden variables, not even Feynman paths. The wave function is an element of a well defined state space, which is neither a classical particle, nor a classical field. Its nature is fully and accurately defined by studying how it evolves and interacts and this is the only way that it can be completely and correctly understood. The evolution and interaction is accurately described by the Schrbdinger equation or the Heisenberg equation or the Feynman propagator or any other representation of the dynamical equation. [Pg.28]

The E-state indices may define chemical spaces that are relevant in similarity/ diversity search in chemical databases. This similarity search is based on atom-type E-state indices computed for the query molecule [55]. Each E-state index is converted to a z score, Z =(% -p )/0 , where is the ith E-state atomic index, p is its mean and O is its standard deviation in the entire database. The similarity was computed with the EucHdean distance and with the cosine index and the database used was the Pomona MedChem database, which contains 21000 chemicals. Tests performed for the antiinflamatory drug prednisone and the antimalarial dmg mefloquine as query molecules demonstrated that the chemicals space defined by E-state indices is efficient in identifying similar compounds from drug and drug-tike databases. [Pg.103]

This exercise underscores one more time that there is no unique way to define state variables. Since our objective here is to understand the association between transfer function and state space models, we will continue our introduction with the ss2tf () and tf2ss o functions. [Pg.234]

The use of step () and impulse () on state space models is straightforward as well. We provide here just a simple example. Let s go back to the numbers that we have chosen for Example 4.1, and define... [Pg.235]

A partial differential equation is then developed for the number density of particles in the phase space (analogous to the classical Liouville equation that expresses the conservation of probability in the phase space of a mechanical system) (32>. In other words, if the particle states (i.e. points in the particle phase space) are regarded at any moment as a continuum filling a suitable portion of the phase space, flowing with a velocity field specified by the function u , then one may ask for the density of this fluid streaming through the phase space, i.e. the number density function n(z,t) of particles in the phase space defined as the number of particles in the system at time t with phase coordinates in the range z (dz/2). [Pg.235]

The classical problem is no less daunting The initial state is defined in terms of the 3N coordinates and 3N momenta of the N particles, which together define a 6iV-dimensional phase space. Each point in this phase space defines a specific microstate. Evolution of the system is described by the trajectory of the starting point through phase space. Not only is it beyond the capabilities of the most powerful computer to keep track of these fluctuations, but should only one of the starting parameters be defined incorrectly, the model fatally diverges very rapidly from the actual situation. [Pg.407]

The phase space for three-dimensional motion of a single particle is defined in terms of three cartesian position coordinates and the three conjugate momentum coordinates. A point in this six-dimensional space defines the instantaneous position and momentum and hence the state of the particle. An elemental hypothetical volume in six-dimensional phase space dpxd Pydpzdqxdqydqz, is called an element, in units of (joule-sec)3. For a system of N such particles, the instantaneous states of all the particles, and hence the state of the system of particles, can be represented by N points in the six-dimensional space. This so-called /r-space, provides a convenient description of a particle system with weak interaction. If the particles of a system are all distinguishable it is possible to construct a 6,/V-dimensional phase space (3N position coordinates and 3N conjugate momenta). This type of phase space is called a E-space. A single point in this space defines the instantaneous state of the system of particles. For / degrees of freedom there are 2/ coordinates in /i-space and 2Nf coordinates in the T space. [Pg.433]

Geometric control is based in a coordinate transformation defined in the state space. This coordinate change allows the transformation of the affine system (3) into a called normal form, which can be partially or totally linearizable. However, how to know the degree of linearizability of the affine system In other words, how to know if the affine system is partially or totally linearizable Next, some notions are defined in order to answer this question. [Pg.175]

Diagnostic observers consist in the definition of a set of observers from which it is possible to define residuals specific of only one failure [8]. Parity relations are relations derived from an input-output model or a state-space model [11] checking the consistency of process outputs and known process inputs. [Pg.205]

When the steady state becomes unstable, the system moves away from it and often undergoes sustained oscillations around the unstable steady state. In the phase space defined by the system s variables, sustained oscillations generally correspond to the evolution toward a limit cycle (Fig. 1). Evolution toward a limit cycle is not the only possible behavior when a steady state becomes unstable in a spatially homogeneous system. The system may evolve toward another stable steady state— when such a state exists. The most common case of multiple steady states, referred to as bistability, is of two stable steady states separated by an unstable one. This phenomenon is thought to play a role in differentiation [30]. When spatial inhomogeneities develop, instabilities may lead to the emergence of spatial or spatiotemporal dissipative stmctures [15]. These can take the form of propagating concentration waves, which are closely related to oscillations. [Pg.258]

The formulation described above provides a useful framework for treating feedback control of combustion instability. However, direct application of the model to practical problems must be exercised with caution due to uncertainties associated with system parameters such as and Eni in Eq. (22.12), and time delays and spatial distribution parameters bk in Eq. (22.13). The intrinsic complexities in combustor flows prohibit precise estimates of those parameters without considerable errors, except for some simple well-defined configurations. Furthermore, the model may not accommodate all the essential processes involved because of the physical assumptions and mathematical approximations employed. These model and parameter uncertainties must be carefully treated in the development of a robust controller. To this end, the system dynamics equations, Eqs. (22.12)-(22.14), are extended to include uncertainties, and can be represented with the following state-space model ... [Pg.361]

I. is the identity matrix and z is defined by z (k-v)AT), is determined. In the second step, this model is transformed into a discrete-time state space model. This is achieved by making an approximate realization of the markov parameters (the impulse responses) of the ARX model ( ). The order of the state space model is determined by an evaluation of the singular values of the Hankel matrix (12.). [Pg.150]

The Transition State Hypothesis. The general idea that a transition state is located at a saddle point on the PES, as detailed in Section 1.3, is familiar to most organic chemists. However, the original concept of a transition state started out as something rather different. In the development of both transition state and RRKM theory, the transition state was defined as the location of a plane (actually a hyperplane) in phase space, perpendicular to the reaction coordinate. ... [Pg.938]

Now we consider more general shortcuts in the state space with the intermediate state defined by... [Pg.70]

The state of a classical system can be completely described by specifying the positions and momenta of all particles. Space being three-dimensional, each particle has associated with it six coordinates - a system of N particles is thus characterized by 6N coordinates. The 6N-dimensional space defined by these coordinates is called the phase space of the system. At any instant in time, the system occupies one point in phase space... [Pg.70]

In order to define the correct state space for a qubit, one must determine... [Pg.307]

The set of states and the probability distribution together fully define the stochastic variable, but a number of additional concepts are often used. The average or expectation value of any function /(X) defined on the same state space is... [Pg.5]

The idea that a universal principle should be able to provide the a priori probability in each case and thereby establish the link between the mathematical probability and the actual world, lost ground during the nineteenth century. An important argument was that in the case of a continuous state space the prescription is not even well-defined since it depends on the choice of variable. A uniform distribution in velocity space is not the same as a uniform distribution in the energy scale. This difficulty has been beautifully demonstrated by Bertrand ). Take a fixed circle of... [Pg.20]

Averages are defined for functions A on the same state space such a function consists of a sequence... [Pg.31]


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See also in sourсe #XX -- [ Pg.3 ]




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