Big Chemical Encyclopedia

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

Articles Figures Tables About

Normal-order sequence

The normal orderly sequence of events in cardiac contraction is initiated by a primary pacemaker, the sinoatrial (SA) node,21 which is located near the surface at the junction of the right atrium and the superior vena cava. One of its properties is automaticity. The normal firing frequency is 60-100 impulses/minute. The established rhythm is conducted to the atrioventricular (AV) node. This node serves to slow the beat somewhat so that atrial contraction can occur before the ventricle is stimulated. The AV node is in the septum (dividing wall) between the atria. The impulse is conducted from the AV node to a common bundle of fibers (Bundle of His) that cross the right atrium to the left ventricle. From there a division of fibers directs impulses along the septum dividing the ventricles, down to the lateral walls and the apex of the heart. The branching of the common bundle leads into the Purkinje fibers that innervate the heart musculature of the ventricles. [Pg.479]

Extended normal-order sequence of operator strings 201... [Pg.177]

Of course, the number of permutations, which are required to bring a given operator string into a certain sequence, determines the sign of the expression Each interchange of two (particle-hole) creation or annihilation operators leads to an additional phase factor (—1) and, possibly, to a contraction of terms. For applications, therefore, it is reasonable to define a (so-called) normal-order sequence which specifies the relative position of the (particle-hole) creation or annihilation operators more precisely we write this sequence symbolically as... [Pg.190]

With this notation and the vacuum amplitudes (46), we can summarize the result of this section by saying that the wave operator as well as any effective operator and matrix element can be written always as perturbation expansion, independent of the particular shell structure of the system. More often than not, moreover, we shall be interested only in the vacuum amplitudes on the rhs of Eq. (46), i.e. only in the completely contracted terms of the operator product [(fl) Aeff(fl ) ], once it has been brought into its normal-order sequence. In fact, these are the... [Pg.200]

If applied to the reference state normal order enables us immediately to recognize those terms which survive in the computation of the vacuum amplitudes. The same applies for any model function and, hence, for real multidimensional model spaces, if a proper normal-order sequence is defined for all the particle-hole creation and annihilation operators from the four classes of orbitals (i)-(iv) in Subsection 3.4. In addition to the specification of a proper set of indices for the physical operators, such as the effective Hamiltonian or any other one- or two-particle operator, however, the definition and classification of the model-space functions now plays a crucial role. In order to deal properly with the model-spaces of open-shell systems, an unique set of indices is required, in particular, for identifying the operator strings of the model-space functions (a)< and d )p, respectively. Apart from the particle and hole states (with regard to the many-electron vacuum), we therefore need a clear and simple distinction between different classes of creation and annihilation operators. For this reason, it is convenient for the derivation of open-shell expansions to specify a (so-called) extended normal-order sequence. Six different types of orbitals have to be distinguished hereby in order to reflect not only the classification of the core, core-valence,... orbitals, following our discussion in Subsection 3.4, but also the range of summation which is associated with these orbitals. While some of the indices refer a class of orbitals as a whole, others are just used to indicate a particular core-valence or valence orbital, respectively. [Pg.201]

With this definition of the orbital indices, we now say that any (given) string of creation and annihilation operators obeys an extended normal-order sequence,... [Pg.202]

In fact, the definition of the extended normal-order sequence (50) is very crucial to our implementation of the GOLDSTONE program. Therefore, in order to make this convention more transparent for the reader, let us consider the effective one-particle part of the operator (47), F = /). Using the definitions of the... [Pg.202]

Brings an operator expression into normal-order i.e. into an extended normal-order-sequence as defined in Eq. (50). [Pg.208]

Bose has described reactions between acid chlorides 214 and Schiff bases 215 where the stereoselectivity depends on the order of addition of the reagents (Scheme 9.68) [117]. When the condensation was conducted by a normal addition sequence (i.e. acid chloride last), only the cis /1-lactam (216b) was formed. However,... [Pg.335]

Systematic error is evident in the clear ellipticity of the distribution. The time ordered sequence shows a non-random "walk" between systematic error quadrants. An excursion from one systematic quadrant to another and a subsequent return is evident. The distribution is non-normal, with too few points in the central region. [Pg.266]

Routing and Production Monitoring In some facilities, batches are individually scheduled. However, in most facilities, production is scheduled by product runs (also called process orders), where a run is the production of a stated quantity of a given product. From the stated quantity and the standard yield of each batch, the number of batches can be determined. As this is normally more than one batch of product, a production run is normally a sequence of some number of batches of the same product. [Pg.48]

Almost all elements form thermodynamically stable halides. The normal stability sequence is F > Cl > Br >1, which in covalent compounds follows the expected order of bond strengths, and in ionic compounds that of the lattice energies. The thermodynamic stability of fluorides (and the kinetic reactivity of F2) is... [Pg.178]

The development of a qualified down-scale model of a process module is integral to the approach of process validation using bench-scale experiments, as described earlier. We have developed down-scale models of process steps ranging from various types of process chromatography for protein purification to separation by precipitation and filtration. These down-scale models have been utilized to evaluate the effects of relevant process parameters on product-quality attributes. The normal logical sequence of process development, of course, is bench scale to pilot scale to full scale. However, for many plasma protein purification processes, a reverse order needs to be followed. As licensed full-scale processes already exist, the full-scale process steps need to be scaled down to construct small process models in order to evaluate the robustness of process parameters on the product without impacting full-scale production. These models can also be utilized to evaluate process changes, improvements, and optimizations easily and economically. [Pg.123]

Ordering implies a comparison, and instead of actual structures, one normally compares sequences of numbers characterizing a molecular graph of a chemical structure. Frequently the required sequences are derived from an enumeration of selected graph invariants. If the selected invariants lead to integers, then the ordering theory of Muirhead (1903) is most suited for these special cases ... [Pg.14]

These five phases are true smectic phases and in normal phase sequences would be expected to be found in the order shown in Scheme I the nematic and isotropic (I) phases are included for completeness. [Pg.201]

Bose has described reactions between acid chlorides ISl and Schiff bases 152 in which the stereoselectivity depends on the order of addition of the reagents (Scheme 5.42) [86]. When the condensation was conducted by a normal addition sequence (i.e. acid chloride last), only the cis /i-lactam 153a was formed. If, however, the inverse addition technique (triethylamine last) was used, 30% cis 153a and 70% trans 153b yS-lactams were obtained under the same conditions. When the reaction was conducted in a microwave oven with chlorobenzene as the solvent, the ratio of trans 153b to cis 153a yS-lactams was 90 10, irrespective of the order of addition, and isomerization to the thermodynamically more stable trans j8-lactam 153b did not occur. [Pg.266]

In general, a given sequence of creation and annihilation operators is said to be normal ordered, if all the creation operators appear left of all annihilation operators. Such an ordering of the operator strings simplifies the manipulation of operator products as well as the evaluation of their matrix elements, as the action of these operators can be read off immediately. In the particle-hole formalism, its hereby obvious that we can annihilate only those particles or holes which exist initially in fact, an existing hole is nothing else than that there is no electron in this hole state. In this formalism, therefore, an operator in second quantization is normal ordered with regard to the reference state [Pg.190]

Evaluation of the operator products as they occur either on the rhs of fhe Bloch Eq. (23) or in fhe definifion of fhe effective operators (15) and (49). The aim of this step is to bring all the creation and annihilation operators (in each term of the expansions) into the extended normal-order form (50). The resulf is a sequence of normal-ordered operator ferms (briefly referred to as Feynman-Goldstone diagrams). [Pg.204]


See other pages where Normal-order sequence is mentioned: [Pg.190]    [Pg.191]    [Pg.196]    [Pg.198]    [Pg.209]    [Pg.190]    [Pg.191]    [Pg.196]    [Pg.198]    [Pg.209]    [Pg.875]    [Pg.169]    [Pg.453]    [Pg.257]    [Pg.258]    [Pg.324]    [Pg.306]    [Pg.394]    [Pg.439]    [Pg.48]    [Pg.699]    [Pg.449]    [Pg.449]    [Pg.138]    [Pg.439]    [Pg.166]    [Pg.204]    [Pg.391]    [Pg.23]    [Pg.131]    [Pg.879]    [Pg.207]   
See also in sourсe #XX -- [ Pg.190 ]




SEARCH



Normal-order sequence extended

© 2024 chempedia.info