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Polarization mixed

Arosolvan process. A/-meth5i-2-pyrr a polar mixing compo-nent, either NMP—glycol, 60 vertical multi-stage the quantity of mix-ing... [Pg.78]

HPC exhibited a notable increase in adsorption with increasing NaCl concentration. Entrapment in the interlayer of recovered sodium montmorillonite did not vary with salinity the extent of entrapment was greater with the 4 M.S. HE and HP celluloses than either of the 2.0 M.S. polymers. Mixed ethers of HEC (2 M.S.) containing an anionic (carboxymethyl) or cationic (3-0-2-hydroxypropyltrimethylaramonium chloride) group at 0.4 M.S. levels did not adsorb from fresh water. Adsorption of these polar mixed ethers increased with increasing electrolyte until electrostatic and solvation effects were negated in 0.54N NaCl solutions and the adsorbed amounts typical of a 2 M.S. HEC were observed. Interlayer entrapments comparable to the equivalent M.S. HEC were observed at lower (0.18N) electrolyte concentrations. [Pg.95]

Hartmann-Hahn match, and cross-polarization mixing time are discussed in relation to obtaining quantitative NMR results. [Pg.118]

Figure 3.36. Different types of holographic gratings, (a) Both writing beams have the same polarization intensity grating. (b) The writing beams are left and right circularly polarized linear polarization grating, (c) The writing beams are s and p polarized mixed-polarization grating. Figure 3.36. Different types of holographic gratings, (a) Both writing beams have the same polarization intensity grating. (b) The writing beams are left and right circularly polarized linear polarization grating, (c) The writing beams are s and p polarized mixed-polarization grating.
Fig. 11 0 Competition by ligands for Ihe ir bonding d orbilul of a central metal atom. Relative overtop is symbolized by the shaded areas, (a) Equal aod strong tr bonds resulting from equal and good overlap of Ihe two carbon monoxide sr orbitals with the meial J orbital (b) Superior overlap of carbon monoxide t orbital wilh polarized metal d orbiial compared lo poorer overlap between ligand <1 and metal d orbitals. Polarization (mixing of higher energy wave functions) occurs so as to maximize total overlap Recall that the overlap integral includes both spatial and intensive properties Ihe represemation above is a graphic simplification. Fig. 11 0 Competition by ligands for Ihe ir bonding d orbilul of a central metal atom. Relative overtop is symbolized by the shaded areas, (a) Equal aod strong tr bonds resulting from equal and good overlap of Ihe two carbon monoxide sr orbitals with the meial J orbital (b) Superior overlap of carbon monoxide t orbital wilh polarized metal d orbiial compared lo poorer overlap between ligand <1 and metal d orbitals. Polarization (mixing of higher energy wave functions) occurs so as to maximize total overlap Recall that the overlap integral includes both spatial and intensive properties Ihe represemation above is a graphic simplification.
In this section we give a brief description of the generalized scheme of NOPO. As an entangler we consider the combination of two processes in a triply resonant cavity, namely, the type-II parametric down-conversion in y ( 2)-medium and polarization mixing between subharmonics in lossless symmetric quarter-wave plate. The Hamiltonian describing intracavity interactions is... [Pg.109]

Centrosymmetric crystals can be transformed into chiral or polar mixed crystals and this enables us to obtain novel means for absolute asymmetric synthesis. The principle is based on selective introduction of a guest molecule into a centrosymmetric host structure, thus reducing the symmetry of the mixed crystal. Crystallization of (E)-cinnamamide (space group P2i/c) in the presence of (E)-... [Pg.10]

These matrix elements express the strong polarization-mixing effects that are observed in resonant scattering from magnetized samples. The occurrence of optical activity crucially depends on the orientation of m relative to the incident... [Pg.11]

Figure 6 Polymerization of bioactive functionalized monomers using polar mixed reaction solvents, (a) Polymerization of unprotected carbohydrate-functionalized oxanorbornene monomers, (b) Poiymerization of cyclooctene monomers bearing sulfated carbohydrates using highly active catalyst 9. (c) Peptide-functionalized norbornene monomers were polymerized using defined cataiyst 10. DCE, 1,2-dichloroethane Pbf, 2,2,4,6,7-pentamethyl-dihydrobenzofuran-5-sulfonyi. Figure 6 Polymerization of bioactive functionalized monomers using polar mixed reaction solvents, (a) Polymerization of unprotected carbohydrate-functionalized oxanorbornene monomers, (b) Poiymerization of cyclooctene monomers bearing sulfated carbohydrates using highly active catalyst 9. (c) Peptide-functionalized norbornene monomers were polymerized using defined cataiyst 10. DCE, 1,2-dichloroethane Pbf, 2,2,4,6,7-pentamethyl-dihydrobenzofuran-5-sulfonyi.

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See also in sourсe #XX -- [ Pg.119 ]




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