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Void Evidence

The occurrence of voids has been thoroughly documented in thick laminates [2], In almost all cases, they are apparently associated with the prepreg surface. The exact mechanism of void formation depends on the system, but in the most general case it can include mechanical entrapment as well as nucleation of stable voids in the resin phase. [Pg.185]


FIG. 47 A 45 ° FIB micrograph of the tin nodule shown in Fig. 46, which has been milled out on three sides by an FIB beam to show the microstructure of the tin film in regions around the nodule structure. Note the voiding evident at the film/substrate interface. (Courtesy of G. Galyon and L. Palmer, IBM Corporation.)... [Pg.906]

Evidence suggests that there is a threshold tensile stress at which void nucleation occurs and spall fracture initiates. Materials subject to transient internal tensions can support tensile stresses significantly in excess of this threshold level, however. Such behavior is a consequence of kinetics and inertia associated with the nucleation and growth of voids during spall. A fairly large body of experimental and theoretical literature on spall phenomena exists and many aspects of the effect are reasonably well understood. Review articles on spall (Curran et al., 1977 Davision and Graham, 1979 Curran, 1982 Meyer and Aimone, 1983 Novikov, 1981) provide access to most of the literature on the subject. [Pg.267]

The interlayer voids are frequently attacked, to yield a periodic sequence of filled and empty spaces. The stage of a compound is defined as the ratio of host layers to guest layers, so that a first-stage compound, in which every interlayer void is filled, is the most concentrated. There is evidence that the staging concept may be, to some extent, an idealization, as is illustrated in Fig. 2. [Pg.282]

Monte Carlo simulations and energy minimization procedures of the non-bonding interactions between rigid molecules and fixed zeolite framework provide a reasonable structural picture of DPP occluded in acidic ZSM-5. Molecular simulations carried out for DPB provide evidence of DPB sorption into the void space of zeolites and the preferred locations lay in straight channels in the vicinity of the intersection with the zigzag channel in interaction with H+ cation (figure 1). [Pg.378]

Although many designs and materials to date have shown promise, some limitations are becoming evident. Pre-formed synthetics fail to fill the entire void space following removal of the NP, leaving open the potential for device migration... [Pg.210]

In Fig. 25b, the simulated marker particles were released from the bottom surface, which generates path lines that show more detail of the flow inside the WS, at lower radial coordinate values. The path lines reinforce the trends seen in Fig. 25a, and it is also possible to see some evidence of flow through the center voids of the particles. Most evident is the mix of spiraling and axial flow between the center front and center right particles. [Pg.369]

We now have clear evidence that selenium can be introduced specifically into proteins as selenocysteine and into a subset of tRNA species as mnm Se U or Se2U. The pathways and molecular mechanisms for insertion of selenium into these molecules have been well established in several model systems, the best studied being E. coli. The role for selenium in selenoproteins (i.e., the need for selenium over sulfur) is thought to be its ability to act as a more reactive nucleophile and perhaps a more rapid catalyst. However, a void in our knowledge exists for the specific need for selenium-modified tRNAs. Mutation of either selD or ybbB did not alter the growth characteristics of E. coli- however, no thorough analysis of the bacterial stress response has been carried out in any of these mutants. Clearly, further study is needed to better define the role for selenium in wobble codon usage for a subset of tRNA species. [Pg.139]

After either oral or intravenous administration of [ Cjondansetron to rats the majority (about 80 %) of the radioactive dose is voided in the faeces, the remainder of the dose being excreted in the urine. In the dog, faecal elimination accounts for about half of the dose and is independent of the route of administration. Evidence from animals with cannulated bile-ducts indicates that the major route of excretion is via the bile. In both species, less than 5 % of the dose is excreted unchanged in urine, suggesting that extensive metabolism of ondansetron occurs. [Pg.263]

The results show that Au is distributed throughout the specimens and ionic Au is partly associated with a root void and possibly filaments (rootlets) within the specimen. This is the first direct evidence for ionic Au in any regolith material and is consistent with Au mobilisation within the rhizosphere. Natural ionic Au species in... [Pg.72]


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