For titanium oxide

Most precursors used for titanium oxide preparation, especially for film production, are based on titanium alkoxides. A variety of mixed enolate-aUcoxide titanium complexes exist, such as 26a-f, 27, 28 and 29a-e, which are typical CVD precursors for titanium oxide. 

Let us finally turn to a brief discussion of the third term, Ti02 (i.e., titanium dioxide). Ti02 has three different crystal structures [18] rutile, anatase, and brookite only the former two of them are commonly used in photocatalysis. Like for many other metal oxides (also for titanium oxide) have the respective structural, optical, and electronic properties... 

The standard dissolution procedure for titanium oxides is the ammonium sulfate-sulfuric acid mixture developed by Rahm [24]. The most commonly used method in industry is based on the use of metallic aluminum as the reductant, and ferric ammonium sulfate as the titrant. The use of ferric ion as the reagent is preferred, since relatively few species will interfere with its reaction with reduced titanium solutions. 

Figure 2.9. The qualitative behavior of the ground state energy of titanium oxide and nickel oxide calculated with a VB model that includes some ionic contribution (amount X). A pure valence bond wavefunction has = 0 and a molecular orbital state has A = 1. For titanium oxide the MO model predicts an energy closer to the real value than a VB calculation. For nickel oxide the valence bond model is more realistic.

For titanium oxides and zinc oxides, similar hydrolysis and dissolution processes must be considered [39, 41] ... 

Table 4. Comparison of calculated (Calc) and experimental (Exp) unit cell parameters and bulk moduli for titanium oxides according to the MS-Q model (Swamy and Gale 2000).

Titanium oxide monolayer on y-AljOj is a potential support for noble metals [1-4]. Many studies have shown that two-dimensional transition metal oxide overlayers are formed when one metal oxide (Vj05, Nb205, MoOj, etc.) is deposited on an oxide support (AljOj, TiO, etc.) [5-7]. The influence of the molecular structures of surface metal oxide species on the catalytic properties of supported metal oxide catalyst has been examined [8-9]. It has been demonstrated that the formation and location of the surface metal oxide species are controlled by the surface hydroxyl chemistry. Moreover, thin-layer oxide catalysts have been synthesized on alumina by impregnation technique with alkoxide precursor [10]. It has been found for titanium oxide, by using Raman spectroscopy, that a monolayer structure is formed for titanium contents below 17% and that polymeric titanium oxide surface species only posses Ti-O-Ti bonds and not Ti=0 bonds. Titanium is typically ionic in its oxy-compounds, and while it can exist in lower oxidation states, the ionic form TF is generally observed in octahedral coordination [11-12]. However, there is no information available about the Ti coordination and structure of this oxide in a supported monolayer. In this work we have studied the structural evolution of the titanium oxy-hydroxide overlayer obtained from alkoxide precursor, during calcination. 

For titanium oxides low in oxygen, more powerful methods must be employed, as will be seen below. 

The numbers of papers focusing on the determination of inorganic UV filters is very scarce, perhaps due to the fact that only two compounds, Ti02 and ZnO, are currently used as UV filters. Atomic spectroscopy techniques, such as atomic absorption spectromety (AAS) (Mason, 1980), inductive coupled plasma atomic emission spectrometry (ICP-AES) (Salvador et al, 2000) and X-ray fluorescence spectrometry (XRFS) (Kawauchi et al, 1996) have been used for titanium oxide determination, whereas to our knowledge zinc oxide has only been determined by AAS (Salvador et al, 2000). 

Titanium forms dihalides TiXj, for example titanium(II) chloride, formed by heating titanium metal and the tetrachloride to about 1200 K. TiCl2 is a black solid, which disproportionates on standing to TiCl4 + Ti. Since it reduces water to hydrogen, there is no aqueous chemistry for titanium(II). A solid oxide TiO is known. 

Titanium dioxide is extensively used for both house paint and artist s paint, because it is permanent and has good covering power. Titanium oxide pigment accounts for the largest use of the element. Titanium paint is an excellent reflector of infrared, and is extensively used in solar observatories where heat causes poor seeing conditions. 

The apparent viscosity, defined as du/dj) drops with increased rate of strain. Dilatant fluids foUow a constitutive relation similar to that for pseudoplastics except that the viscosities increase with increased rate of strain, ie, n > 1 in equation 22. Dilatancy is observed in highly concentrated suspensions of very small particles such as titanium oxide in a sucrose solution. Bingham fluids display a linear stress—strain curve similar to Newtonian fluids, but have a nonzero intercept termed the yield stress (eq. 23) ... 

Commercial metal anodes for the chlorine industry came about after the late 1960s when a series of worldwide patents were awarded (6—8). These were based not on the use of the platinum-group metals (qv) themselves, but on coatings comprised of platinum-group metal oxides or a mixture of these oxides with valve metal oxides, such as titanium oxide (see Platinum-GROUP metals, compounds Titanium compounds). In the case of chlor-alkaH production, the platinum-group metal oxides that proved most appropriate for use as coatings on anodes were those of mthenium and iridium. 

Ruthenium—Titanium Oxides. The x-ray diffractioa studies of mthenium—titanium oxide coatiags show that the coatiag components are preseat as the metal dioxides, each ia the mtile form as weU as ia soHd solutioa with each other (13). The developmeat of the crystal stmcture begias to occur at a bake temperature of about 400°C. By foUowiag the diffractioa line for the mtile stmcture, an iacrease ia crystallinity can be seen as temperatures are iacreased to the 600—700°C range. Above these temperatures, the peak begias to separate iato two separate peaks, iadicative of phase separatioa iato iadividual mtile oxides, oae rich ia mthenium and one rich ia titanium. 

EBHP is mixed with a catalyst solution and fed to a horizontal compartmentalized reactor where propylene is introduced into each compartment. The reactor operates at 95—130°C and 2500—4000 kPa (360—580 psi) for 1—2 h, and 5—7 mol propylene/1 mol EBHP are used for a 95—99% conversion of EBHP and a 92—96% selectivity to propylene oxide. The homogeneous catalyst is made from molybdenum, tungsten, or titanium and an organic acid, such as acetate, naphthenate, stearate, etc (170,173). Heterogeneous catalysts consist of titanium oxides on a siUca support (174—176). 

For resistance to actinic degradation, the use of certain forms of titanium oxide is an alternative to chrome salts. Another approach has been the use of polymerized methylol melamine on cotton (145). In this case, the action of sunlight leads to gradual breakdown of the melamine polymer after several years. After this, actinic degradation of cotton proceeds as it does in unprotected cotton. 

Precipitation of a hydrated titanium oxide by mixing aqueous solutions of titanium chloride with alkaU forms the precipitation seeds, which are used to initiate precipitation in the Mecklenburg (50) variant of the sulfate process for the production of pigmentary titanium dioxide. Hydrolysis of aqueous solutions of titanium chloride is also used for the preparation of high purity (>99.999%) titanium dioxide for electroceramic appHcations (see Ceramics). In addition, hydrated titanium dioxide is used as a pure starting material for the manufacture of other titanium compounds. 

Iron Titanates. Ferrous metatitanate [12168-52-4] FeTiO, mp ca 1470°C, density 472(0), an opaque black soHd having a metallic luster, occurs in nature as the mineral ilmenite. This ore is used extensively as a feedstock for the manufacture of titanium dioxide pigments. Artificial ilmenite may be made by heating a mixture of ferrous oxide and titanium oxide for several hours at 1200°C or by reducing a titanium dioxide/ferric oxide mixture at 450°C. 

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

The role of antimony oxide is not entirely understood. On its own it is a rather weak fire retardant although it appears to function by all of the mechanisms listed above. It is, however, synergistic with phosphorus and halogen compounds and consequently widely used. Other oxides are sometimes used as alternatives or partial replacements for antimony oxide. These include titanium dioxide, zinc oxide and molybdenic oxide. Zinc borate has also been used. 

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