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V K-edge XANES spectra of a Vj05-Ti02 catalyst , Mn, -1V2 2xMo2jt06

V KI curves of three alumina with different grain sizes, obtained by the Double T orsion method .

V Ki diagram of a polycrystalline zirconia ceramic .

V Ki laws and SEM micrographs of HAP before ageing water at 37 C during

V l signal amplifier

V l-19. Absorption coefficients of 1I02. is given in units of I mol 1 cm, base 10, room temperature. The absorption spectrum is obtained by the flash photolysis of mixtures ll2 , lie, and 02. The continuous nature of the spectrum indicates a repulsive upper state. From I lochanadel ct al. , reprinted by permission. Copyright 1072 by the American Institute of Physics.

V l-I9. Absorption coollicicnls of IIOj, is given in units of I mol cin , base It , room temperature. The absorption spectrum is obtained by the flash photolysis of mixtures II2O, I le, and O2. The continuous nature of the spectrum iiidieates a repulsive upper stale. From I loehanadel el al. 72 by the American Institute of Physics.

V lead-acid battery

V lead-add battery

V lead-add battery relationship of discharge time with energy density and Ah capacity

V liquid state NMR spectra of the synthesis gels of V-MFI samples after aging. A, V-MFI,

V maintenance-free semi-sealed SLI track battery.

V MAS NMR of 3.5wt vanadium V0, Al203 catalyst after calcination at 700 C. Spinning rate 14kHz. Bo 9.40T.

V MAS NMR of8wt vanadium VO AbOs catalyst prior to reaction . Spinning rate 14kHz. 60 9.40T.

V MAS NMR spectra of three different VO, Ti02 catalysts. Vanadia loadings are 6wt V2O5. Adapted from ref reprinted with permission from the American Chemical Society.

V MAS NMR spectra, the peaks to negative intensity correspond to Al atoms in the support.

V MAS spectra of the uncalcined and calcined 5 V-MCM samples For comparison, of crystalline V O, is shown

V mEP for Cl para-H2 surface vs. reaction coordinates.

V NMR of TMP adsorbed on mTS-1.0 and H-mTS-1.0 mesoporous Ti02-Si02 catalysts .

V NMR shift vs. pH in four ionic media.

V NMR spectra at different V

V NMR spectra of a series of V2O5 catalysts supported on Ti02 Zr02 after heating at 250 C for 2 h. showing the evolution of the distorted octahedral V-0 species , by permission of the

V NMR spectra of media and cell-associated firactions of the yeast S. cerevisiae exposed to 5.0 mM vanadate at pH 4.0 . The arrow indicates the chemical shift of the orthovanadate resonance at -541 ppm. Reproduced ft om with permission from the American Chemical Society.

V NMR spectrum of sodium cholate-treated human hemolysate. Resonance assignments for the phospholipids indicated on the spectra were confirmed by adding authentic phospholipids to the NMR samples and selective hydrolysis of alkenylacyl Lipids 3 . 765-770.

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