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Head stacking

Fig. 52. Schematic illustrations of three possibilities of head-to-head stacking of sorboyl groups in aggregates of lipid 27 [367]... Fig. 52. Schematic illustrations of three possibilities of head-to-head stacking of sorboyl groups in aggregates of lipid 27 [367]...
The alkaline earth metal cations with a large diameter (Sr, Ba ) and benzo-15-crown-5 stilbene derivatives are characterized by the formation of the 2 1 sandwich-type complexes (Scheme 10). In the case of Ba2+ the sandwich complex possesses the highest stability. According to the NMR studies and X-ray analysis of the sandwich complex of 8, molecules of dye are arranged in a head-to-head stacking. [Pg.242]

Deep-Well Turbine and Canned Version. By stacking up the stages, heads up to 1100 m (3500 ft) can be achieved. The deep-weU pump is submerged into the weU, and Hquid comes into contact with the pump body and the weU walls. Alternatively, a pump pit may be of dry design, and a can, ie, an enclosure around the pump, having connections to the source of Hquid is provided (Fig. 9). [Pg.294]

Fig. 2. Rigid foam laminating line 1, material tank 2, agitator 3, metering pump 4, heat exchanger 5, bottom facet toU 6, bottom facet alignment device 7, top facet toU 8, top facet alignment device 9, mixing head 10, traverse assembly 11, top nip toU 12, bottom nip toU 13, take-up conveyor top belt with adjustable height 14, take-up conveyor bottom belt 15, curing oven 16, laminate 17, side-trim saws 18, cutoff saw (traversing) 19, laminated-panel stack... Fig. 2. Rigid foam laminating line 1, material tank 2, agitator 3, metering pump 4, heat exchanger 5, bottom facet toU 6, bottom facet alignment device 7, top facet toU 8, top facet alignment device 9, mixing head 10, traverse assembly 11, top nip toU 12, bottom nip toU 13, take-up conveyor top belt with adjustable height 14, take-up conveyor bottom belt 15, curing oven 16, laminate 17, side-trim saws 18, cutoff saw (traversing) 19, laminated-panel stack...
When comparable amounts of oil and water are mixed with surfactant a bicontinuous, isotropic phase is formed [6]. This bicontinuous phase, called a microemulsion, can coexist with oil- and water-rich phases [7,1]. The range of order in microemulsions is comparable to the typical length of the structure (domain size). When the strength of the surfactant (a length of the hydrocarbon chain, or a size of the polar head) and/or its concentration are large enough, the microemulsion undergoes a transition to ordered phases. One of them is the lamellar phase with a periodic stack of internal surfaces parallel to each other. In binary water-surfactant mixtures, or in... [Pg.686]

Effects of performance changes, 201-203 Head curve for single pump, 198 Relations between head, horsepower, capacity and speed, 200 Temperature rise 207-209 Viscosity corrections, 203-207 Purging, flare stack systems, 535 Reciprocating pumps, 215—219 Flow patterns, 219 Specification form, 219 Relief areas, 437 External fires, 451, 453 Sizing, 434, 436... [Pg.629]

Crystals of benzoic acid contain pairs of molecules held together head to head by hydrogen bonds. These pairs then stack in planes that are held together by dispersion forces. [Pg.776]

P2j Z = 2 D = 1.57 R = 0.048 for 931 intensities. The base exists in the thioxo form, with C-8=S and N-7 protonated. The 8-thio substituent causes the base to assume the syn (—102.6°) orientation. The o-ribosyl group is 2T3 (174.8 °, 44.1 °). The exocyclic, C-4 -C-5 bond orientation is trans (—173.2°). This does not favor intramolecular hydrogen-bonding of 0-5 to N-3 of the syn base. The C=S distance is 166.8 pm. The S atom is involved in a weak, acceptor hydrogen-bond to a water molecule, S H-O(w) = 361 pm. The bases are stacked head-to-tail, with overlap of the C=S bonds and the purine ring, in contrast to the known, related structure l-/ -D-ribofuranosyl-2-thioxo-3ff-benzimidazole,197 where similar head-to-tail stacking of the bases involves overlap of the base rings only. [Pg.318]

C36H60O30,C3H7O3S-,Na+,9 H20 Cyclomaltohexaose-sodium 1-pro-panesulfonate, nonahydrate (ACDPRS)129 P212121 Z= 2 Dx = 1.42 R = 0.08 for 2,219 intensities. This structure is a channel type, with the molecules of cyclomaltohexaose stacked head-to-tail. It is almost isomorphous with the sodium benzenesulfonate complex.275... [Pg.354]

The assay sashay is like betting on coin tosses with the following rules. We toss two coins. If the first one comes up heads, I win, and the second coin is irrelevant. If the first one comes up tails, we have to decide whether the toss counts. To do that, we look at the second coin. If it also comes up tails, the toss does not count and we call it a draw. With these rules, I will win 50 per cent of the time and it will be a draw 25 per cent of the time. You win only if both the first coin comes up heads and the second comes up tails, which will only happen 25 per cent of the time. So the odds are heavily stacked in my favour. If you doubt this, please get in touch. I will be happy to play you for real money. Using these standards to judge the effectiveness of a medication is voodoo science to the nth degree. [Pg.53]

Figure 7.4 is a photograph of a portion of the peptide controls slide printer. A stack of microscope slides, ready for printing, is at the far left. The slides are automatically ejected from the stack, one at a time. The slides are moved on a conveyer to the right, positioning them under the print head. The print head has eight nozzles, out of which microliter-sized droplets are ejected onto an underlying slide. The slide conveyer then places a new slide under the nozzles, and the process repeats. [Pg.130]

The crystal structures of (EDT-TTFBr2)2MX4 and (EDO-TTFBr2)2MX4 are quite similar, although the space group symmetry is different in these two systems. However, this difference comes only from the conformation of terminal six-membered rings of the donor molecules, which plays no important role in the physical properties of the present salts. The donor molecules are stacked in a head-to-tail manner to form quasi-one-dimensional columns as shown in Fig. 6a. [Pg.88]

FIGURE 31 -10 Cerebral amino acids and carbohydrates incorporate 13C label from infused glucose. The top panel shows a 13C NMR spectrum obtained from a gray-matter-rich volume in the human head. (From reference [141].) The right panel shows label incorporation into brain glycogen and glucose in humans. (From reference [142].) The stack plot illustrates the rate of label incorporation into many compounds and carbons in the rat brain. (From reference [ 143].) In all studies, glucose labeled at the 1 or 6 position was administered intravenously. [Pg.552]


See other pages where Head stacking is mentioned: [Pg.45]    [Pg.253]    [Pg.67]    [Pg.403]    [Pg.382]    [Pg.317]    [Pg.95]    [Pg.45]    [Pg.253]    [Pg.67]    [Pg.403]    [Pg.382]    [Pg.317]    [Pg.95]    [Pg.350]    [Pg.513]    [Pg.299]    [Pg.104]    [Pg.152]    [Pg.160]    [Pg.194]    [Pg.197]    [Pg.50]    [Pg.366]    [Pg.716]    [Pg.226]    [Pg.149]    [Pg.853]    [Pg.1339]    [Pg.797]    [Pg.160]    [Pg.160]    [Pg.155]    [Pg.161]    [Pg.172]    [Pg.164]    [Pg.210]    [Pg.233]    [Pg.267]    [Pg.313]    [Pg.354]    [Pg.1]    [Pg.208]    [Pg.45]   
See also in sourсe #XX -- [ Pg.198 ]




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