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Titanium analysis

These can be used where the additive has an element that is clearly different from the filler, and where the amount of additive is sufficient for the sensitivity of the technique being employed. Thus, carbon analysis can be used for many additives on silica surfaces, and titanium analysis is possible for organo-titanates on many fillers. This approach does not distinguish between surface and admixed additive though. [Pg.159]

Madey and co-workers followed the reduction of titanium with XPS during the deposition of metal overlayers on TiOi [87]. This shows the reduction of surface TiOj molecules on adsorption of reactive metals. Film growth is readily monitored by the disappearance of the XPS signal from the underlying surface [88, 89]. This approach can be applied to polymer surfaces [90] and to determine the thickness of polymer layers on metals [91]. Because it is often used for chemical analysis, the method is sometimes referred to as electron spectroscopy for chemical analysis (ESCA). Since x-rays are very penetrating, a grazing incidence angle is often used to emphasize the contribution from the surface atoms. [Pg.308]

Figure C2.17.6. Transmission electron micrograph and its Fourier transfonn for a TiC nanocrystal. High-resolution images of nanocrystals can be used to identify crystal stmctures. In tliis case, tire image of a nanocrystal of titanium carbide (right) was Fourier transfonned to produce tire pattern on tire left. From an analysis of tire spot geometry and spacing, one can detennine that tire nanocrystal is oriented witli its 11001 zone axis parallel to tire viewing direction [217]. Figure C2.17.6. Transmission electron micrograph and its Fourier transfonn for a TiC nanocrystal. High-resolution images of nanocrystals can be used to identify crystal stmctures. In tliis case, tire image of a nanocrystal of titanium carbide (right) was Fourier transfonned to produce tire pattern on tire left. From an analysis of tire spot geometry and spacing, one can detennine that tire nanocrystal is oriented witli its 11001 zone axis parallel to tire viewing direction [217].
The second form consists of Pt metal but the iridium is present as iridium dioxide. Iridium metal may or may not be present, depending on the baking temperature (14). Titanium dioxide is present in amounts of only a few weight percent. The analysis of these coatings suggests that the platinum metal acts as a binder for the iridium oxide, which in turn acts as the electrocatalyst for chlorine discharge (14). In the case of thermally deposited platinum—iridium metal coatings, these may actually form an intermetallic. Both the electrocatalytic properties and wear rates are expected to differ for these two forms of platinum—iridium-coated anodes. [Pg.121]

There are many colorimetric methods used for trace analysis of peroxides using reagents such as ferrous ion, leuco base of methylene blue, yy -diphenylcarbohydrazide, titanium(IV), iodide ion, and Ai,A7-dimethyl- -phenylenediamine. The latter two are the most commonly used reagents... [Pg.132]

The analytical chemistry of titanium has been reviewed (179—181). Titanium ores can be dissolved by fusion with potassium pyrosulfate, followed by dissolution of the cooled melt in dilute sulfuric acid. For some ores, even if all of the titanium is dissolved, a small amount of residue may still remain. If a hiU analysis is required, the residue may be treated by moistening with sulfuric and hydrofluoric acids and evaporating, to remove siUca, and then fused in a sodium carbonate—borate mixture. Alternatively, fusion in sodium carbonate—borate mixture can be used for ores and a boiling mixture of concentrated sulfuric acid and ammonium sulfate for titanium dioxide pigments. For trace-element deterrninations, the preferred method is dissolution in a mixture of hydrofluoric and hydrochloric acids. [Pg.134]

The 1-alkoxytitatranes can be synthesized by the reaction of equimolar amounts of tetraalkyl titanates and triethanolamine (105). X-ray crystallographic analysis of the soHd isolated from the reaction of one mole of triethanolamine and one mole of TYZOR TPT confirms the stmcture as a centrosymmetric dimer having a Ti isopropoxy nitrilotriethoxy ratio of 1 1 1. The titanium atoms have achieved a coordination number of six via a rather unsymmetrical titanium—oxygen bridge (106). [Pg.147]

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%. [Pg.437]

Such significant increase of accuracy may be explained on the base of analysis of the numerical values of the theoretical correction coefficients and calculated for 1, , and for analytical pai ameter lQ.j,yipj.j,jj- Changing from lines intensities for the ratios of analytical element line intensity to the intensity of the line most effecting the result of analytical element (chromium in this case) measurement enables the decreases of the error 5 or even 10 times practically to the level of statistics of the count rate. In case of chromium the influencing elements will be titanium, tungsten or molybdenum. [Pg.442]

The first equation ignores the existence of the intermediate titanium oxides, which is reasonable for this analysis of die oxidation mechanism.)... [Pg.267]

B. A. Prine, Analysis of Titanium/Carbon Steel Heat Exchanger Fire, Paper presented at AIChE Loss Prevention Symposium, Aug. 1991. [Pg.46]

A chiral titanium complex with 3-cinnamoyl-l,3-oxazolidin-2-one was isolated by Jagensen et al. from a mixture of TiCl 2(0-i-Pr)2 with (2R,31 )-2,3-0-isopropyli-dene-l,l,4,4-tetraphenyl-l,2,3,4-butanetetrol, which is an isopropylidene acetal analog of Narasaka s TADDOL [48]. The structure of this complex was determined by X-ray structure analysis. It has the isopropylidene diol and the cinnamoyloxazolidi-none in the equatorial plane, with the two chloride ligands in apical (trans) position as depicted in the structure A, It seems from this structure that a pseudo-axial phenyl group of the chiral ligand seems to block one face of the coordinated cinnamoyloxazolidinone. On the other hand, after an NMR study of the complex in solution, Di Mare et al, and Seebach et al, reported that the above trans di-chloro complex A is a major component in the solution but went on to propose another minor complex B, with the two chlorides cis to each other, as the most reactive intermediate in this chiral titanium-catalyzed reaction [41b, 49], It has not yet been clearly confirmed whether or not the trans and/or the cis complex are real reactive intermediates (Scheme 1.60). [Pg.39]

A solution of 1.0 mmol of 2-acetyl alkenoate in 2.5 mL of CH2C1, is added slowly to a solution of 4.0 mmol of titanium(IV) chloride in 7.5 mL of CH-CL under an atmosphere of nitrogen at — 78 °C. The mixture instantaneously turns deep red. and is stirred at — 78 °C before being quenched by the addition of 5 mL of sat. aq potassium carbonate. The mixture is then partitioned between 10 mL of bt20 and 10 mL of water. The aqueous phase is extracted with three 10-mL portions of Et2(), and the extracts are combined, washed with 10 mL of brine, and dried over anhyd potassium carbonate. Concentration under reduced pressure gives the crude product. Product analysis is by capillary GC. [Pg.351]

Tin plate, thickness of tin coating on, determination by x-ray spectrography, 148, 149, 157, 158 Tissues, determination of dry weight by absorptiometry, 297-300 Tissue sections, biological, determination of mineral elements in, 301-305 Titanium, as internal standard in vanadium determination, 188 determination by x-ray emission spectrography, 222, 329 trace analysis by x-ray emission spectrography, 163, 225-229 Topaz, as analyzing crystal, 116-118, 220, 318-327 Total reflection, 112, 117... [Pg.354]

The reduction of gun erosion by the use of additives to the gun powder has been studied at the US Naval Ordnance Station (NOS), Indian Head, Md. During the investigation of one of the additives, namely titanium dioxide (Ti02) or Swedish additive, it was necessary to determine small amts of Ti in gun powder residues taken from the gun after firing. As only very small amts of Ti were expected in the samples, the very sensitive technique of NAA was used for the analysis (Ref 2)... [Pg.365]

Chemical vapor deposition processes are complex. Chemical thermodynamics, mass transfer, reaction kinetics and crystal growth all play important roles. Equilibrium thermodynamic analysis is the first step in understanding any CVD process. Thermodynamic calculations are useful in predicting limiting deposition rates and condensed phases in the systems which can deposit under the limiting equilibrium state. These calculations are made for CVD of titanium - - and tantalum diborides, but in dynamic CVD systems equilibrium is rarely achieved and kinetic factors often govern the deposition rate behavior. [Pg.275]

As an example of the use of MIXCO.TRIAD, an analysis of comonomer triad distribution of several ethylene-propylene copolymer samples will be delineated. The theoretical triad Intensities corresponding to the 2-state B/B and 3-state B/B/B mixture models are given In Table VI. Abls, et al (19) had earlier published the HMR triad data on ethylene-propylene samples made through continuous polymerization with heterogeneous titanium catalysts. The data can be readily fitted to the two-state B/B model. The results for samples 2 and 5 are shown In Table VII. The mean deviation (R) between the observed and the calculated Intensities Is less than 1% absolute, and certainly less than the experimental error In the HMR Intensity determination. [Pg.184]


See other pages where Titanium analysis is mentioned: [Pg.1126]    [Pg.275]    [Pg.1126]    [Pg.275]    [Pg.543]    [Pg.120]    [Pg.324]    [Pg.134]    [Pg.432]    [Pg.468]    [Pg.4]    [Pg.263]    [Pg.268]    [Pg.655]    [Pg.237]    [Pg.176]    [Pg.315]    [Pg.967]    [Pg.973]    [Pg.826]    [Pg.131]    [Pg.1268]    [Pg.410]    [Pg.696]    [Pg.761]    [Pg.44]    [Pg.32]    [Pg.104]    [Pg.112]    [Pg.122]    [Pg.454]    [Pg.81]    [Pg.105]    [Pg.158]   
See also in sourсe #XX -- [ Pg.292 ]




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