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Fusion Linear systems

An extensive review of linear systems, including several topics (Z-pinches, liners, fusion burners...) not discussed in this paper, was given by Krakowski. In addition, the reader is referred to proceedings of two conferences on linear systems held in the United States in 1977. [Pg.214]

At the present time, the long linear open field line systems discussed above do not appear to be particularly attractive for pure fusion systems, due primarily to high axial particle and/or energy loss rates as well as other difficulties relating to both physics and technology issues. As fission-fusion hybrid systems the outlook is not so pessimistic and, indeed, linear systems possess virtues that may make them quite attractive for such an application. [Pg.229]

Based on the relatively poor pure fusion reactor outlook for long linear devices, U.S. Department of Energy support of such work was virtually eliminated at the end of 1979. Certain elements of the linear program having relevance to other ongoing fusion projects were continued (e.g., multiple mirror confinement studies), while in other instances, a natural transition was made from open linear systems research to closed system (CT) studies. [Pg.229]

There remain several very interesting aspects of linear systems physics clearly worthy of investigation. In view of the relatively small amount of funds available for non-mainline fusion research, however, it appears unlikely that experiments of the scale required to establish proof-of-principle will be carried out. [Pg.229]

As pointed out by Flory [16], the principle of equal reactivity, according to which the opportunity for reaction (fusion or scission) is independent of the size of the participating polymers, implies an exponential decay of the number of polymers of size / as a function of /. Indeed, at the level of mean-field approximation in the absence of closed rings, one can write the free energy for a system of linear chains [11] as... [Pg.520]

The dynamic mechanical behavior indicates that the glass transition of the rubbery block is basically independent of the butadiene content. Moreover, the melting temperature of the semicrystalline HB block does not show any dependence on composition or architecture of the block copolymer. The above findings combined with the observation of the linear additivity of density and heat of fusion of the block copolymers as a function of composition support the fact that there is a good phase separation of the HI and HB amorphous phases in the solid state of these block copolymers. Future investigations will focus attention on characterizing the melt state of these systems to note if homogeneity exists above Tm. [Pg.152]

Fig. 4.1. Fundamentals of the ubiquitin system. Adapted from Ref [5]. Figure 4.1 shows the fundamentals of the ubiquitin system. (1) Ubiquitin is synthesized in linear chains or as the N-terminal fusion with small ribosomal subunits that are cleaved by de-ubiquitylating enzymes to form the active protein. Ubiquitin is then activated in an ATP-dependent manner by El where a thiolester linkage is formed. It is then transthiolated to the active-site cysteine of an E2. E2s interact with E3s and with substrates and mediate either the indirect (in the case of HECT E3s) or direct transfer of ubiquitin to substrate. A number of factors can affect this process. We know that interactions with Hsp70 can facilitate ubiquitylation in specific instances and competition for lysines on substrates with the processes of acetylation and sumoylation may be inhibitory in certain instances. (2) For efficient proteasomal targeting to occur chains of ubiquitin linked internally through K48 must be formed. This appears to involve multiple... Fig. 4.1. Fundamentals of the ubiquitin system. Adapted from Ref [5]. Figure 4.1 shows the fundamentals of the ubiquitin system. (1) Ubiquitin is synthesized in linear chains or as the N-terminal fusion with small ribosomal subunits that are cleaved by de-ubiquitylating enzymes to form the active protein. Ubiquitin is then activated in an ATP-dependent manner by El where a thiolester linkage is formed. It is then transthiolated to the active-site cysteine of an E2. E2s interact with E3s and with substrates and mediate either the indirect (in the case of HECT E3s) or direct transfer of ubiquitin to substrate. A number of factors can affect this process. We know that interactions with Hsp70 can facilitate ubiquitylation in specific instances and competition for lysines on substrates with the processes of acetylation and sumoylation may be inhibitory in certain instances. (2) For efficient proteasomal targeting to occur chains of ubiquitin linked internally through K48 must be formed. This appears to involve multiple...
In addition to this discussion of "planar Moebiane" and the one earlier in this chapter of "linear Moebiane" and its cylindrical counterpart, attention is now directed to some other selected molecules of mathematical interest. Although the existence of molecules, formed by the edge fusion of benzene modules (generally referred to as "benzenoids"), in which it is not possible to assign a coherent system of conjugated single and double bonds that span the molecule was illustrated in Chapter 2, these have always had an odd number of "triple points" [59] e.g., see phenalene ( 11 in Table 1 of... [Pg.160]

The formation of linearly fused tricycles serves to illustrate a variant of the SDNC. In these systems (28) the double bond must be directed away from both ring fusions. This was accomplished by placing the silyl group at a ring position again poised to direct the collapse of the intermediate cation (29 equation 20). [Pg.765]

Magnus was the first to develop extensive synthetic applications of the Pauson-Khand preparation of the bicyclo[3.3.0]oct-l-en-3-one system. His efforts amply demonstrate the degree to which the high level of functionality in the Pauson-Khand products can be directly utilized in building more complex structures. A formal synthesis of the antitumor sesquiterpene coriolin illustrates a very efficient sequence for construction of the third ring in the linearly fused triquinane series in the presence of considerable functionality (Schemes 10 and 18). A synthesis of the related triquinane hirsutic acid utilizes the observation that the proper stereochemical relationship between the substituents at C-7 and the ring-fusion carbon (C-5) of the bicyclo[3.3.0]oct-l-en-3-one system, while not controllable in the cycloaddition reaction itself, may be readily established by acid- or base-catalyzed equilibration (equation 54 and Scheme 19). ... [Pg.1060]

Starch is a polysaccharide formed by two polymers of glucose linear amylose and branched amylopectin. The gelatinization process can be regarded as a fusion of fhe crystalline starch regions in the presence of enough wafer and heafing. Starch retrogradation is a recrystallization process that is controlled by diffusion and depends on solute mobility in the system. [Pg.312]


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Fusion linear systems, application

Fusion systems

Linear systems

Linearized system

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