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Hydration, continuous

Hooton (H48) noted some pitfalls in the experimental determination of permeabilities and in the practical utilization of the results. In an experimental determination, accurate results will not be obtained unless the sample has been vacuum saturated and, even if it is, equilibrium flow in accordance with d Arcy s law may not occur because water is being used up to continue hydration. In practice, a concrete sample is probably not often saturated throughout if it is not, capillary forces, as well as the pressure difference. alTect the rate of flow. Applications of results obtained with pastes to concrete are further complicated by the presence in the latter of cracks, poorly compacted areas and other inhomogeneities. [Pg.274]

Nephrotoxicity may be prevented or diminished by prehydration with 21 of normal saline administered over a 6-8 h period, followed by continued hydration during and after the cisplatin infusion. Nausea and vomiting may be managed with antiemetics. Electrolyte concentration should be monitored and supplemented as needed. Treatment for an anaphylactic reaction would include antihistamines, administered with or without epinephrine. If accidental exposure to the eyes or skin occurs, the affected skin area should be washed thoroughly with soap and water, and eyes should be flushed with copious amounts of tepid water for at least 15 min. Seizures should be treated with diazepam, lorazepan, phenobarbital, or phenytoin. [Pg.616]

The air management system is shown in Fig. 7.1b. A side channel compressor is used for low pressure experiments (below 130 kPa), while a centralized air compression plant is used to study the effect of ah pressure on stack performance (between 130 and 250 kPa). An important issue to be considered is the cell humidification to guarantee that the stack works properly, since the electrolyte membrane needs to be continuously hydrated (see Sects. 3.2 and 4.5). That humidification is... [Pg.199]

Phase Transitions in Lipid Assemblies. The rich polymorphism of amphiphilic systems, of which the multilamellar and the Hn phases are only two structures, was made evident from the seminal work of Luzzati and co-workers. Since that early work, an immense variety of water-induced phase transitions have been observed and rationalized in terms of an apparently systematic connection between water content and polar group molecular area. Therefore, the recent observation of a double transition—Hn to lamellar back to Hn—from continual hydration of dioleoylphosphatidyl-ethanolamine (40) was a surprise. Furthermore, an estimate of the cost of uncurling the monolayer in the formation of bilayers based on the previously described bending modulus far exceeds the osmotic work that actually produced the transition. Although this transition sequence can successfully be accounted for by simple thermodynamical principles, it, in fact, contains many geometry-dependent free energy contributions that we simply do not yet understand (41). [Pg.191]

The structure of the 4BS paste at a distance of about 250 pm from the plate surface changes after 2 h of soaking in 1.25 rel. dens. H2SO4 solution (see Fig. 9.28). Figure 9.28a shows a picture of a 4BS crystal with hydrated and then partially sulfated surface. At a certain pH level, 4BS crystals react with water forming hydroxy-sulfates in the form of small particles (Fig. 9.28b). The latter may merge with the hydrated layers of the adjacent 4BS crystals (Fig. 9.28a). Thus, a continuous hydrated porous structure is formed, which is then sulfated. [Pg.435]

As already mentioned in previous sections, the sulfonic acid groups in PFSA membranes exhibit remarkably high acidity. In the presence of water, the membrane hydrates to form a continuous hydrated domain in which protons are solvated by water with the inunobDized anionic group (R-SOs ) as counter-ions [8], High italic conductivity of Nafion membranes can also be achieved in solvent environments other than pure water. In 1994, the first attempt was made to... [Pg.53]

Figure 5.4 Modelling the influences of the modulus of the fibre (a) and its diameter (b) on the changes in strength of FRC composites over time, due to continued hydration leading to the densening and strengthening of the ITZ (after Katz [26]). Figure 5.4 Modelling the influences of the modulus of the fibre (a) and its diameter (b) on the changes in strength of FRC composites over time, due to continued hydration leading to the densening and strengthening of the ITZ (after Katz [26]).

See other pages where Hydration, continuous is mentioned: [Pg.1489]    [Pg.251]    [Pg.460]    [Pg.87]    [Pg.245]    [Pg.334]    [Pg.616]    [Pg.667]    [Pg.37]    [Pg.42]    [Pg.109]    [Pg.109]    [Pg.431]    [Pg.35]    [Pg.345]    [Pg.192]    [Pg.242]    [Pg.318]    [Pg.156]    [Pg.40]    [Pg.336]    [Pg.424]    [Pg.425]    [Pg.645]    [Pg.175]   
See also in sourсe #XX -- [ Pg.243 ]




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Alkenes continued) hydration

Azines—continued bicyclic, covalent hydration

Continuous hydration-condensation reaction

Covalent hydration continuous-flow technique

Covalent hydration—continued

Covalent hydration—continued of 1,3,6,8-tetraazanaphthalene

Covalent hydration—continued of pteridines

Covalent hydration—continued of pteridines, amino

Covalent hydration—continued of pteridines, chloro

Covalent hydration—continued of pteridines, dihydro

Covalent hydration—continued of pteridines, hydroxy

Covalent hydration—continued of pteridines, mercapto

Covalent hydration—continued of purines

Covalent hydration—continued of pyrazinopyrazines

Covalent hydration—continued of quinazoline 3-oxides

Covalent hydration—continued of quinazolines

Covalent hydration—continued of tetraazanaphthalenes

Covalent hydration—continued of triazanaphthalenes

Covalent hydration—continued qualitative aspects

Covalent hydration—continued quantitative aspects

Covalent hydration—continued rapid-reaction technique

Covalent hydration—continued rate of equilibration

Covalent hydration—continued ring-opening

Covalent hydration—continued spectra, changes

Covalent hydration—continued test for

Pyridine—continued hydrates

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