Pockets

The shaded areas in Fig. 6.24, known as pockets, represent areas of additional process-to-process heat transfer. Remember that the profile of the grand composite curve represents residual heating and cooling demands after recovering heat within the shifted temperature intervals in the problem table algorithm. In these pockets in Fig. 6.24, a local surplus of heat in the process is used at temperature differences in excess of AT ,in to satisfy a local deficit. ... 

Figure 15.4 A plant for the production of animal feed. The heat pump encroaches into a pocket in the gremd composite curve. (From Smith and Linnhojf, Trans. IChemE, ChERD, 66 195, 1988 reproduced by permission of the Institution of Chemical Engineers.)...

The war itself also drove the development of improved and miniaturised electronic components for creating oscillators and amplifiers and, ultimately, semiconductors, which made practical the electronic systems needed in portable eddy current test instruments. The refinement of those systems continues to the present day and advances continue to be triggered by performance improvements of components and systems. In the same way that today s pocket calculator outperforms the large, hot room full of intercormected thermionic valves that I first saw in the 50 s, so it is with eddy current instrumentation. Today s handheld eddy current inspection instrument is a powerful tool which has the capability needed in a crack detector, corrosion detector, metal sorter, conductivity meter, coating thickness meter and so on. 

All metal parts exposed to the room are made of stainless steel and motors and transmissions are IP 65 to withstand the eflfect of the cleaning agents. The design also takes into account the special considerations necessary for food processing machinery with regards to easy accessibility to all parts and the lack of corners, edges, pockets or other food traps , so that the mechanical system can be easily cleaned. 

We noted in Section VII-2B that, given the set of surface tension values for various crystal planes, the Wulff theorem allowed the construction of fhe equilibrium or minimum firee energy shape. This concept may be applied in reverse small crystals will gradually take on their equilibrium shape upon annealing near their melting point and likewise, small air pockets in a crystal will form equilibrium-shaped voids. The latter phenomenon offers the possible advantage that adventitious contamination of the solid-air interface is less likely. 

Extraction of a ligand from the binding pocket of a protein. The force (represented by an arrow) applied to the ligand (shown in van der Waals spheres) leads to its dissociation from the binding pocket of the protein (a slice of the protein represented as a molecular surface is shown). 

The simulations also revealed that flapping motions of one of the loops of the avidin monomer play a crucial role in the mechanism of the unbinding of biotin. The fluctuation time for this loop as well as the relaxation time for many of the processes in proteins can be on the order of microseconds and longer (Eaton et al., 1997). The loop has enough time to fluctuate into an open state on experimental time scales (1 ms), but the fluctuation time is too long for this event to take place on the nanosecond time scale of simulations. To facilitate the exit of biotin from its binding pocket, the conformation of this loop was altered (Izrailev et al., 1997) using the interactive molecular dynamics features of MDScope (Nelson et al., 1995 Nelson et al., 1996 Humphrey et al., 1996). 

We assume in the following that the ligand is bound in a binding pocket of depth 6 —a = 7 A involving a potential barrier AU = 25 kcal/mol, similar to that of streptavidin (Chilcotti et al., 1995). We also assume that the diffusion coefficient of the ligand is similar to the diffusion coefficient of the heme group in myoglobin (Z) = 1 A /ns) as determined from Mofibauer spectra (Nadler and Schulten, 1984). 

The molecular surface of receptor site regions cannot be derived from the structure infoi mation of the molecule, bth represents the form ofthe active site of a protein surrounded by a ligand. This surface representation is employed in drug design in order to illustrate the volume of the pocket region or the molecular interaction layers [186. ... 

The distillation heads Fig. 22(F) and Fig. 22(G) can be fitted with thermometers having a ground-glass cone just above the bulb (Fig. 22(M)). These are expensive, and it is usually more convenient to fit a thermometer pocket (Fig. 22(N)) which consists of a small well , fitting as shown into the neck of the flask. A small volume of mercury is placed in the well just to cover the bulb of a conventional thermometer, and thus provides excellent thermal contact between the thermometer and the sides of the pocket. 

Enzyme like binding pocket 3-t-2 addition of OSO4 to olefin. 

To explain how solid acids such as Nafion-H or HZSM-5 can show remarkable catalytic activity in hydrocarbon transformations, the nature of activation at the acidie sites of such solid acids must be eon-sidered. Nafion-H contains acidic -SO3H groups in clustered pockets. In the acidic zeolite H-ZSM-5 the active Bronsted and Tewis acid sites are in close proximity (—2.5 A). 

Heating Kemp s acid with appropriate aromatic diamines yields bis-imides with two convergently oriented carboxylic acid groups on the edges of a hydrophobic pocket. Dozens of interesting molecular complexes have been obtained from such compounds and can be traced in the Journal of the American Chemical Society under the authorship of J. Rebek, Jr., (1985 and later e.g. T. Tjivikua, 1990 B). 

When we consider sources of methane we have to add old methane methane that was formed millions of years ago but became trapped beneath the earth s surface to the new methane just de scribed Firedamp an explosion hazard to miners oc curs in layers of coal and is mostly methane Petroleum deposits formed by microbial decomposi tion of plant material under anaerobic conditions are always accompanied by pockets of natural gas which IS mostly methane... 

To test the null hypothesis, you reach into your pocket, retrieve a penny, and determine its mass. If the mass of this penny is 2.512 g, then you have proved that the null hypothesis is incorrect. Finding that the mass of your penny is 3.162 g, however, does not prove that the null hypothesis is correct because the mass of the next penny you sample might fall outside the limits set by the null hypothesis. 

Occlusions, which are a second type of coprecipitated impurity, occur when physically adsorbed interfering ions become trapped within the growing precipitate. Occlusions form in two ways. The most common mechanism occurs when physically adsorbed ions are surrounded by additional precipitate before they can be desorbed or displaced (see Figure 8.4a). In this case the precipitate s mass is always greater than expected. Occlusions also form when rapid precipitation traps a pocket of solution within the growing precipitate (Figure 8.4b). Since the trapped solution contains dissolved solids, the precipitate s mass normally increases. The mass of the precipitate may be less than expected, however, if the occluded material consists primarily of the analyte in a lower-molecular-weight form from that of the precipitate. 

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