Titanium spectra

Figure 22 presents the spectra of the common oxides of titanium. The two common forms of TiOj, anatase and rutile, give clearly distinguishable spectra. These distinctions in the spectra have been confirmed in several samples extending over a wide range of crystallite size. The packing within the first coordination shells of anatase and rutile is different and may account for the spectral differences. The tetravalent titanium spectra are... 

Explain the appearance of this titanium spectrum of a solution of TiCU. obtained at 25.55 MHz in a 9.4 T magnet. The scale markers are 1000 Hz each. 

Surface concentration data show that the effective thickness of /Mactoglobulin on gold is approximately 15 A. A reduced intensity by a factor of two of the Amide II bands in the titanium spectrum indicates that even thinner films are formed on this surface. 

Figure B2.1.3 Output of a self-mode-locked titanium-sapphire oscillator (a) non-collinear intensity autocorrelation signal, obtained with a 100 pm p-barium borate nonlinear crystal (b) intensity spectrum.

Samples were tested on in a melt of salts (75% Na SO, 25% NaCl) at 950°C in an air atmosphere for 24 hours. Micro X-rays spectrum by the analysis found that the chemical composition of carbides of an alloy of the ZMI-3C and test alloys differs noticeably. In the monocarbide of phase composition of an alloy of the ZMI-3C there increased concentration of titanium and tungsten is observed in comparison with test alloys containing chemical composition tantalum. The concentration of more than 2% of tantalum in test alloys has allowed mostly to deduce tungsten from a mono carbide phase (MC) into solid solution. Thus resistance of test alloys LCD has been increased essentially, as carbide phase is mostly sensitive aggressive environments influence. The critical value of total molybdenum and tungsten concentration in MC should not exceed 15%. 

Consider first blue sapphire Al203 Ti(III), Fe(III) (Fig. 2). In the absence of Fe(III) the absorption spectrum is easy to interpret. The weak band with a maximum at about 500 nm is due to the t2 —> e crystal-field transition on Ti(III) (3d ), the strong band at 2<280nm is due to a Ti(III)-0( — II) LMCT transition. The absorption band in the region around 700 nm in the case of the codoped crystal cannot be due to Fe(III). It has been ascribed to MMCT, i.e. to a transition within an iron-titanium pair ... 

Pure pigments and dyes can be identified from their IR spectrum. Some reference spectra are given in the Hummel and Scholl collection [9]. Other than simple white pigments or solvent soluble types, identification of pigments in finished products is particularly difficult. Raman spectroscopy can aid the positive identification of pigments such as titanium dioxide. 

Table 7 shows the calculated weight percent of calcium carbonate and titanium dioxide in the white-colored paint sample. These levels are based on the calcium and titanium levels shown in Table 6. Calcium carbonate was evident by the FTIR spectrum acquired from the dried paint sample, shown in Figure 13. (Flad it been available, Raman spectroscopy, which gives ready access to the low wavenumber region, could have been used to confirm the presence (and polymorphic form) of titanium dioxide [4].) Given the white color of the paint, it is likely that the titanium present was present as titanium dioxide, and this was assumed in the calculations. The calculated weight percentage of calcium carbonate in the dried paint is 21.7 wt%, and 12.6 wt% in the paint containing the solvents. The titanium dioxide levels were calculated to be 30.6 and 17.7 wt% in the dried and solvent-containing paint sample, respectively.

The sunblocks zinc oxide, titanium dioxide, and iron oxide are inorganic chemicals that are not absorbed into the skin. These substances consist of opaque particles that reflect both visible and ultraviolet light. In addition, zinc oxide blocks virtually the entire UVA and UVB spectrum and thus offers overall protection. The particulate nature of these sunblocks enhances their effectiveness at reflecting sunlight. The smaller the particle size, the greater the surface area available for reflection, and the more effective the sun protection offered by the formulation. 

Fragalia and co-workers have reported the details of the He(I) and He(II) excited photoelectron spectra of Cp2Ti(CO)2 and concluded that evidence exists for significant backbonding between the Ti 3d orbitals and empty carbonyl v orbitals. Further, there is no evidence of important overlap between Ti and Cp orbitals. A small electrostatic perturbation of the Cp ligands is caused by the titanium atom (85). Bohm has described an elaborate study of the low energy PE spectrum of Cp2Ti(CO)2 (1) by means of semiempirical MO calculations (86). 

FIGURE 3.9 EPR of titanium citrate. The citrate complex of the Ti(III) ion at pH 9 is a general-purpose strong reductant of metalloproteins. This 3d system gives an S = 1/2 EPR spectrum with. -values just below ge. The axial signal below 3300 gauss is from Ni(I) in factor F-430. 

Because of the high sensitivity of Ti-containing luminescence centers to their local environments, photoluminescence spectroscopy can be applied to discriminate between various kinds of tetrahedral or near-tetrahedral titanium sites, such as perfectly closed Ti(OSi)4 and defective open Ti(OSi)3(OH) units. Lamberti et al. (49) reported an emission spectrum of TS-1 with a dominant band at 495 nm, with a shoulder at 430 nm when the sample was excited at 250 nm. When the excitation wavelength was 300 nm, the emission spectrum was characterized by a dominant band at 430 nm with a shoulder at 495 nm. These spectra and their dependence on the excitation wavelength clearly indicate the presence of two slightly different families of luminescent Ti species, which differ in their local environments, in agreement with EXAFS measurements carried out on the same samples. 

A direct correlation between the concentration of the titanium oxo species and epoxidation activity was proposed by Lin and Frei (133). Loading TS-1/H202 with propene after evacuation, they observed by FTIR difference spectroscopy the loss of the bands characterizing propene (at 1646 cm-1) and TiOOH (at 837 and 3400 cm-1). Figure 48 is the infrared difference spectrum recorded immediately after loading the propene on TS-1/H202 Fig. 49 includes the spectra recorded 80 and 320 min later. 

Spin trapping by PBN has also been employed to detect radical formation in a photo-Kolbe reaction in which acetic acid is irradiated (A > 360 nm) in the presence of platinized titanium dioxide powder (Kraeutler et al, 1978). The nitroxide observed was considered to be (PBN—Me ), but the published spectrum clearly shows the presence of a second species spectral overlap might therefore be an alternative to solvent polarity as an explanation of the discrepancy between the observed splitting parameters and those previously reported for this species. Where poor resolution obtains, it is important that... 

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