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Shell enhancements

Torres and co-workers have investigated the cubic NLO properties of various metallotriazo-lehemiporphyrazines.190-194 Early THG studies at 1,340 nm and 1,907 nm with CHCI3 solutions show that metal ions with partially filled d-shells enhance 7 when compared to the uncomplexed macrocycles.190,191 However, later 1,064 nm THG studies with LB films of some Co11 complexes indicate that metallation has no significant effects on the NLO responses.192 More recently,... [Pg.642]

In support of the entire Metz operation the 8ist Chemical Battalion fired j 1,118 rounds of ammunition. During part of the time a shortage of artillery shell enhanced the role of the 4.2-inch mortar. ... [Pg.477]

It should be noted that solvent co-intercalation took place intensively in EC -I- DEC, in which lithium ion is solvated not only by EC, but also by DEC. In the other solvent systems, lithium ions are solvated exclusively by EC molecules, and solvent co-intercalation was less vigorous. These results may suggest that the degree of solvent co-intercalation is greatly enhanced by the solvation of linear alkyl carbonates such as DEC and DMC to lithium ions. However, it is not easy at present to explain why the presence of linear alkyl carbonates in the solvation shell enhances solvent co-intercalation. More detailed information about the structures and the ion-solvent interactions of lithium ion in non-aqueous solutions are necessary to answer this question. [Pg.214]

The Langevin model has been employed extensively in the literature for various numerical and physical reasons. For example, the Langevin framework has been used to eliminate explicit representation of water molecules [22], treat droplet surface effects [23, 24], represent hydration shell models in large systems [25, 26, 27], or enhance sampling [28, 29, 30]. See Pastor s comprehensive review [22]. [Pg.234]

Petroleum sulfonates are widely used as solubilizers, dispersants (qv), emulsifiers, and corrosion inhibitors (see Corrosion and corrosion inhibitors). More recentiy, they have emerged as the principal surfactant associated with expanding operations in enhanced oil recovery (66). Alkaline-earth salts of petroleum sulfonates are used in large volumes as additives in lubricating fluids for sludge dispersion, detergency, corrosion inhibition, and micellar solubilization of water. The chemistry and properties of petroleum sulfonates have been described (67,68). Principal U.S. manufacturers include Exxon and Shell, which produce natural petroleum sulfonates, and Pilot, which produces synthetics. [Pg.241]

Some processes have large heat transfer requirements. This may result in large inventories of material within the heat transfer equipment. If the material is thermally unstable it would be inherently safer to reduce the residence time in the heat exchanger. Options to minimize heat exchanger inventory include the use of different types of heat exchangers. Inventories in shell and tube heat exchangers can be reduced by the use of turbulators in the tubes to enhance heat transfer coefficients, and by placing the more hazardous material on the tube side. [Pg.71]

The presence of sulfur is found to enhance the formation of graphitic carbon shells around cobalt-containing particles, so that cobalt or cobalt carbide particles encapsulated in graphitic polyhedra are found throughout the soot along with the single-layer nano-... [Pg.53]

Multi-stage preheating, pre-calciners, kiln combustion system improvements, enhancement of internal heat transfer in kiln, kiln shell loss reduction, optimize heat transfer in clinker cooler, use of waste fuels Blended cements, cogeneration... [Pg.755]

In the above example, a relatively complex steam generator of the watertube type has been adopted. Where lower-quality steam for process or fuel heating is required, a simpler shell (or firetube) design may be appropriate. In some cases, supplementary firing may be provided for the boiler, so further increasing plant complexity and with it the need for enhanced control and maintenance requirements. [Pg.198]

At the limiting concentration the enhancer will bind all available water in hydration shells, leaving none to participate in the solution of the drug substance. [Pg.208]

Nanoparticles of Mn and Pr-doped ZnS and CdS-ZnS were synthesized by wrt chemical method and inverse micelle method. Physical and fluorescent properties wra cbaractmzed by X-ray diffraction (XRD) and photoluminescence (PL). ZnS nanopatlicles aniKaled optically in air shows higher PL intensity than in vacuum. PL intensity of Mn and Pr-doped ZnS nanoparticles was enhanced by the photo-oxidation and the diffusion of luminescent ion. The prepared CdS nanoparticles show cubic or hexagonal phase, depending on synthesis conditions. Core-shell nanoparticles rahanced PL intensity by passivation. The interfacial state between CdS core and shell material was unchan d by different surface treatment. [Pg.757]

Fig. 6 shows PL spectra of CdS nanoparticles and CdS-ZnS core-shell nanoparticles. In PL spectrum of CdS nanoparticles, the emission band is seen at around 400nm. The emission band of CdS-ZnS core-shell nanoparticles is higher dian that of CdS ones at around 400nm. The PL enhancement of CdS-ZnS core-shell nanoparticl is due to passivation which means that surface atoms are bonded to the shell material of similar lattice constant and much larger band gap [9], Althou the sur ce treatment conditions are different, the ranission band of CdS-ZnS core-shell nanoparticles is same in PL spectra of Fig. 6(b). This indicates that interfacial state between CdS core and shell material was unchan d by different surfaKs treatment. [Pg.760]

Figure 11. Infrared resonance enhanced photodissociation spectrum of V (OCO)5 obtained by monitoring loss of CO2. The antisymmetric stretch of outer-shell CO2 is near 2349 cm (the value in free CO2, indicated by the dashed vertical line). The vibration shifts to 2375 cm for inner-shell CO2. Figure 11. Infrared resonance enhanced photodissociation spectrum of V (OCO)5 obtained by monitoring loss of CO2. The antisymmetric stretch of outer-shell CO2 is near 2349 cm (the value in free CO2, indicated by the dashed vertical line). The vibration shifts to 2375 cm for inner-shell CO2.

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See also in sourсe #XX -- [ Pg.176 , Pg.177 ]




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