Phase aluminum oxide

Adsorption HPLC is the classification in which the highly polar silica particles are exposed (no adsorbed or bonded liquid phase). Aluminum oxide particles fit this description too and are also readily available as the stationary phase. As mentioned earlier, this classification can also be thought of as normal phase... 

Microstructurc. Crystal size, porosity, and impurity phases play a major role in fixing the fracture characteristics and toughness of an abrasive grain. As an example, rapidly cooled fused aluminum oxide has a microcrystalline stmcture promoting toughness for heavy-duty grinding appHcations, whereas the same composition cooled slowly has a macrocrystalline stmcture more suitable for medium-duty grinding. 

The Beckstead-Derr-Price model (Fig. 1) considers both the gas-phase and condensed-phase reactions. It assumes heat release from the condensed phase, an oxidizer flame, a primary diffusion flame between the fuel and oxidizer decomposition products, and a final diffusion flame between the fuel decomposition products and the products of the oxidizer flame. Examination of the physical phenomena reveals an irregular surface on top of the unheated bulk of the propellant that consists of the binder undergoing pyrolysis, decomposing oxidizer particles, and an agglomeration of metallic particles. The oxidizer and fuel decomposition products mix and react exothermically in the three-dimensional zone above the surface for a distance that depends on the propellant composition, its microstmcture, and the ambient pressure and gas velocity. If aluminum is present, additional heat is subsequently produced at a comparatively large distance from the surface. Only small aluminum particles ignite and bum close enough to the surface to influence the propellant bum rate. The temperature of the surface is ca 500 to 1000°C compared to ca 300°C for double-base propellants. 

Aluminum-containing propellants deflver less than the calculated impulse because of two-phase flow losses in the nozzle caused by aluminum oxide particles. Combustion of the aluminum must occur in the residence time in the chamber to meet impulse expectations. As the residence time increases, the unbumed metal decreases, and the specific impulse increases. The soHd reaction products also show a velocity lag during nozzle expansion, and may fail to attain thermal equiUbrium with the gas exhaust. An overall efficiency loss of 5 to 8% from theoretical may result from these phenomena. However, these losses are more than offset by the increase in energy produced by metal oxidation (85—87). 

The term alumina hydrates or hydrated aluminas is used in industry and commerce to designate aluminum hydroxides. These compounds are tme hydroxides and do not contain water of hydration. Several forms are known a general classification is shown in Figure 1. The most weU-defined crystalline forms ate the trihydroxides, Al(OH) gibbsite [14762-49-3], bayerite [20257-20-9], and nordstrandite [13840-05-6], In addition, two aluminum oxide—hydroxides, AIO(OH), boelimite [1318-23-6] and diaspote [14457-84-2], have been clearly defined. The existence of several other forms of aluminum hydroxides have been claimed. However, there is controversy as to whether they ate truly new phases or stmctures having distorted lattices containing adsorbed or intedameUar water and impurities. 

The vapor-phase conversion of aniline to DPA over a soHd catalyst has been extensively studied (18,22). In general, the catalyst used is pure aluminum oxide or titanium oxide, prepared under special conditions (18). Promoters, such as copper chromite, nickel chloride, phosphoric acid, and ammonium fluoride, have also been recommended. Reaction temperatures are usually from 400 to 500°C. Coke formed on the catalyst is removed occasionally by burning. In this way, conversions of about 35% and yields of 95% have been reported. Carba2ole is frequently a by-product. 

In the dyestuff industry, anthraquinone still ranks high as an intermediate for the production of dyes and pigments having properties unattainable by any other class of dyes or pigments. Its cost is relatively high and will remain so because of the equipment and operations involved in its manufacture. As of May 1991, anthraquinone sold for 4.4/kg in ton quantities. In the United States and abroad, anthraquinone is manufactured by a few large chemical companies (62). At present, only two processes for its production come into consideration manufacture by the Friedel-Crafts reaction utilizing benzene, phthahc anhydride, and anhydrous aluminum chloride, and by the vapor-phase catalytic oxidation of anthracene the latter method is preferred. 

The small (10 -lm) coating particles are typically aluminum oxide [1344-28-1/, Al O. These particles can have BET surface areas of 100 to 300 m /g. The thermal and physical properties of alumina crystalline phases vary according to the starting phase (aluminum hydroxide or hydrate) and thermal treatment (see ALUMINUM COMPOUNDS, ALUMINUM OXIDE). 

The chloroform phase is then removed, the aqueous phase extracted twice more with 200 ml of chloroform and the united extracts shaken out 4 times, each time with 200 ml of 2N sodium hydroxide solution. The alkaline solution is then rendered acid to Congo red reagent, using hydrochloric acid and extracted 3 times with chloroform. After drying over sodium Sulfate and evaporating the solvent, the residue is chromatographed on aluminum oxide (Activity Stage V). The substance eluted with benzene and benzene/chloroform (1 1) is recrystallized from chloroform/hexane (1 1) MP 107° to 109°C. 

Aluminum oxide, A1203, is known almost universally as alumina. It exists with a variety of crystal structures, many of which form important ceramic materials (see Section 14.22). As a-alumina, it is the very hard, stable, crystalline substance corundum impure microcrystalline corundum is the purple-black abrasive known as emery. Some impure forms of alumina are beautiful, rare, and highly prized (Fig. 14.25). A less dense and more reactive form of the oxide is y-alumina. This form absorbs water and is used as the stationary phase in chromatography. 

Alumina - Alumina forms a variety of oxides and hydroxides whose structures have been characterized by X-ray diffraction (16). From the catalytic viewpoint y-alumina is the most important. This is a metastable phase that is produced from successive dehydration of aluminum trihydroxide (gibbsite) to aluminum oxide hydroxide (boehmite) to y-alumina, or from dehydration of boehmite formed hydrothermally. y-alumina is converted into a-alumina (corundum) at temperatures around 1000 C. 

Chapter 3 through Chapter 8 deal with the basic aspects of the practical uses of PLC. Chapter 3 describes sorbent materials and precoated layers for normal or straight phase (adsorption) chromatography (silica gel and aluminum oxide 60) and partition chromatography (silica gel, aluminum oxide 150, and cellulose), and precoated layers for reversed-phase chromatography (RP-18 or C-18). Properties of the bulk sorbents and precoated layers, a survey of commercial products, and examples of substance classes that can be separated are given. 

Aluminum Oxide Bulk Materials for Straight Phase PLC... 

Another fairly important stationary phase in straight phase PLC is aluminum oxide. Comparable with silica gel also in the case of aluminum oxides, hydroxyl groups at the surface of this adsorbent are responsible for the selective retention of sample molecules. The relevant physical parameters for the characterization of aluminum oxides suitable for straight phase PLC are the following ... 

To achieve better separation efficiency and reproducibility compared with handmade layers also in the case of aluminum oxides, precoated plates are available for straight phase PLC. They are listed in Table 3.4. 

Substance classes that can be separated by straight phase adsorption PLC on aluminum oxide stationary phases are, for example, alkaloids [17]. 

Aluminum oxides, similar to silica gels, are available as bulk materials and as precoated plates, to be used not only for straight phase adsorption chromatography, but also for partition PLC (see Table 3.3 and Table 3.4). In particular, the aluminum oxide type 150 (i.e., mean pore diameter 150 A [15 tun]) is suitable for partition chromatographic purposes. 

Porous aluminum oxide can be used as a template for the production of nanowires and nanotubes. For example, metals can be deposited on the pore walls by the following procedures deposition from the gas phase, precipitation from solution by electrochemical reduction or with chemical reducing agents, or by pyrolysis of substances that have previously been introduced into the pores. Wires are obtained when the pore diameters are 25 nm, and tubes from larger pores the walls of the tubes can be as thin as 3 nm. For example, nanowires and nanotubes of nickel, cobalt, copper or silver can be made by electrochemical deposition. Finally, the aluminum oxide template can be removed by dissolution with a base. 

Dang et al. (1994) observed that the experimentally determined solubility lines for Zn2+ in 14 soil solutions from southern Queensland with soil pH from 7.45-8.98 and 0.08-2.07% CaC03 were not undersaturated with respect to the solubility of any known mineral form of Zn. Therefore, they suggested that Zn2+ activity was mainly controlled by adsorption-desorption reactions in these soils. Similar observation on solubility of Cr(VI) in arid soils was reported by Rai et al. (1989). In the absence of a solubility controlling solid phase, Cr(VI) aqueous concentrations under slightly alkaline conditions may be primarily controlled by adsorption/desorption reactions (Rai et al., 1989). Chromuim(VI) is adsorbed by iron and aluminum oxides, and kaolinite and its adsorption decreases with increasing pH. 

Figure 1 shows the powder X-ray diffraction (XRD) pattern of the as-prepared Li(Nio.4Coo.2Mno.4)02 material. All of the peaks could be indexed based on the a-NaFeC>2 structure (R 3 m). The lattice parameters in hexagonal setting obtained by the least square method were a=2.868A and c=14.25A. Since no second-phase diffraction peaks were observed from the surface-coated materials and it is unlikely that the A1 ions were incorporated into the lattice at the low heat-treatment temperature (300°C), it is considered that the particle surface was coated with amorphous aluminum oxide. 

Temperature of the fluidized bed is another parameter that could influence the heat transfer coefficient. Increasing bed temperature affects not only the physical properties of the gas and solid phases, but also increases radiative heat transfer. Yoshida et al. (1974) obtained measurements up to 1100°C for bubbling beds of aluminum oxide particles with 180 pm diameter. Their results, shown in Fig. 6, indicate an increase of over 100% in the heat transfer coefficient as the bed temperature increased from 500 to 1000°C. Very similar results were reported by Ozkaynak et al. (1983) who obtained measurements for bubbling beds of sand particles (dp = 1030 pm) at temperatures up to 800°C. 

As pH rises, the metal content of drainage water tends to decrease. Some metals precipitate directly from solution to form oxide, hydroxide, and oxy-hydroxide phases. Iron and aluminum are notable is this regard. They initially form colloidal and suspended phases known as hydrous ferric oxide (hfo, FeOOH n O) and hydrous aluminum oxide (HAO, AlOOH nH.2O), both of which are highly soluble under acidic conditions but nearly insoluble at near-neutral pH. 

Many barium aluminosilicate-based compositions will eventually react with the chromium oxide or aluminum oxide scales on the metal interconnect or metal edge rails to form barium chromate or a celsian phase at the interface [6], This can cause a mechanical weakness that is easily delaminated. Also, compositions that contain boron can react over time with water (steam) to produce B2(OH)2 or B(OH)3 gas. This can decompose the glass and greatly limit the lifetime of the seal. Thus many of the new investigations have emphasized low or no boron glass compositions. 

Af-dipropyl-p- toluidine, 2 550t a, a -dinitroanthraquinones, 9 315—316 a-alumina, 2 406t 14 103. See also Corundum transition to, 2 403 a-aluminum-iron—silicon alloys, 2 317 intermetallic phases, 2 316t a-aluminum oxide-hydroxide. 

P-aluminum-iron-silicon alloys, 2 317 intermetallic phases, 2 316t P-aluminum oxide-hydroxide. 

Similarly, isomorphous replacement of the A1 atom by Mg atoms in networks of aluminum oxide octahedra leads to a negatively charged lattice. Clays are representative examples where such atomic substitution causes the charge at the phase boundary. Sparingly soluble salts also carry a surface charge because of lattice imperfections. 

Like formaldehyde, acetaldehyde easily forms polymers, in this case paraldehyde and metaldehyde. Paraldehyde will form when hydrochloric or sulfuric acid is added to acetaldehyde. Polymerization of acetaldehyde to mec-aldehyde occurs in the gaseous phase in the presence of aluminum oxide or silicon dioxide catalyst. 

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