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Titanium oxide supports

DOSCH ET AL. Hydrous Titanium Oxide-Supported Catalysts... [Pg.287]

Figure 5 Electron micrograph showing pits in titanium oxide support produced by nickel particles during reaction in 1 Torr hydrogen at 1070 K. Inset shows the electron diffraction pattern of the support under these conditions. Figure 5 Electron micrograph showing pits in titanium oxide support produced by nickel particles during reaction in 1 Torr hydrogen at 1070 K. Inset shows the electron diffraction pattern of the support under these conditions.
Isobutyraldehyde can be synthesized selectively from methanol and ethanol in one step by using titanium oxide-supported vanadium oxide (V205/Ti02) as a catalyst. This catalyst is also capable of synthesizing isobutyraldehyde from methanol and n-propyl alcohol. The reactions of methanol and w-propyl... [Pg.186]

Catalysts such as titanium oxide supported on pumice require activation to function properly. By adding about 2 per cent by volume of nitrogen oxides to a mixture of anthracene vapor containing a four-fold excess of air over that theoretically required oxidation occurs smoothly over titanium oxide at 400° to 500° C.88... [Pg.442]

The principal steps in the process proposed by the UKAEA for recovery of uranium from seawater are shown in Fig. 5.20. The titania recovery system consists of 60 beds, 1.3 ft (0.4 m) deep, each with a flow area of 188,000 ft (17,500 m ), filled with hydrous titanium oxide supported on an inert carrier. The inventory of the entire system is 71 million lb (32.2 million kg) of Ti, valued at 71 million in 1966. [Pg.263]

Huang, S.-Y., Ganesan, R, and Popov, B. N. 2010. Electro catalytic activity and stabihty of niobium-doped titanium oxide supported platinum catalyst for polymer electrolyte membrane fuel cells. Appl. Catal, B 96 224-231. [Pg.29]

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). [Pg.140]

It is carried out in the Hquid phase at 100—130°C and catalyzed by a soluble molybdenum naphthenate catalyst, also in a series of reactors with interreactor coolers. The dehydration of a-phenylethanol to styrene takes place over an acidic catalyst at about 225°C. A commercial plant (50,51) was commissioned in Spain in 1973 by Halcon International in a joint venture with Enpetrol based on these reactions, in a process that became known as the Oxirane process, owned by Oxirane Corporation, a joint venture of ARCO and Halcon International. Oxirane Corporation merged into ARCO in 1980 and this process is now generally known as the ARCO process. It is used by ARCO at its Channelview, Texas, plant and in Japan and Korea in joint ventures with local companies. A similar process was developed by Shell (52—55) and commercialized in 1979 at its Moerdijk plant in the Netherlands. The Shell process uses a heterogeneous catalyst of titanium oxide on siHca support in the epoxidation step. Another plant by Shell is under constmction in Singapore (ca 1996). [Pg.484]

Titanium dioxide supported gold catalysts exhibit excellent activity for CO oxidation even at temperatures as low as 90 K [1]. The key is the high dispersion of the nanostructured gold particles over the semiconducting Ti02 support. The potential applications of ambient temperature CO oxidation catalysts include air purifier, gas sensor and fuel cell [2]. This work investigates the effects of ozone pretreatment on the performance of Au/Ti02 for CO oxidation. [Pg.413]

Recently, it is reported that Xi02 particles with metal deposition on the surface is more active than pure Ti02 for photocatalytic reactions in aqueous solution because the deposited metal provides reduction sites which in turn increase the efficiency of the transport of photogenerated electrons (e ) in the conduction band to the external sjistem, and decrease the recombination with positive hole (h ) in the balance band of Xi02, i.e., less defects acting as the recombination center[l,2,3]. Xhe catalytic converter contains precious metals, mainly platinum less than 1 wt%, partially, Pd, Re, Rh, etc. on cordierite supporter. Xhus, in this study, solutions leached out from wasted catalytic converter of automobile were used for precious metallization source of the catalyst. Xhe XiOa were prepared with two different methods i.e., hydrothermal method and a sol-gel method. Xhe prepared titanium oxide and commercial P-25 catalyst (Deagussa) were metallized with leached solution from wasted catalytic converter or pure H2PtCl6 solution for modification of photocatalysts. Xhey were characterized by UV-DRS, BEX surface area analyzer, and XRD[4]. [Pg.469]

Propose a way to apply titanium oxide in very highly dispersed form onto an alumina support. [Pg.407]

The tltanla-based thin film catalyst models were constructed by first oxidizing the titanium surface In 5 x 10 torr of O2 for approximately 30 minutes at 775 K. This produced an AES llneshape consistent with fully oxidized TIO2. The metal was then vapor deposited onto the oxide support with the latter held at 130 K. The thickness of the metal overlayer and Its cleanliness were verified by AES. After various annealing and adsorption procedures, these thin films were further characterized using SSIMS, AES and TDS. For comparison, some work was done with Pt on Al20s. In this case a Mo foil covered with AI2O3 replaced the Tl(OOOl) substrate. [Pg.81]

The process has been commercially implemented in Japan since 1977 [1] and a decade later in the U.S., Germany and Austria. The catalysts are based on a support material (titanium oxide in the anatase form), the active components (oxides of vanadium, tungsten and, in some cases, of molybdenum) and modifiers, dopants and additives to improve the performance, especially stability. The catalyst is then deposited over a structured support based on a ceramic or metallic honeycomb and plate-type structure on which a washcoat is then deposited. The honeycomb form usually is an extruded ceramic with the catalyst either incorporated throughout the stmcture (homogeneous) or coated on the substrate. In the plate geometry, the support material is generally coated with the catalyst. [Pg.8]

The key effect of oxide supports on the catalytic activities of metal particles is exerted through the interface between oxides and metal particles. The key objective of this study is to develop synthesis methodologies for tailoring this interface. Here, an SSG approach was introduced to modify the surface of mesoporous silica materials with ultrathin films of titanium oxide so that the uniform deposition of gold precursors on ordered mesoporous silica materials by DP could be achieved without the constraint of the low lEP of silica. The surface sol-gel process was originally developed by Kunitake and coworkers.This novel technology enables molecular-scale control of film thickness over a large 2-D substrate area and can be viewed as a solution-based... [Pg.62]


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Hydrous titanium oxide supported

Hydrous titanium oxide supported catalysts

Oxidation supports

Oxide supports

Oxides titanium oxide

Titanium oxide supports hydrous

Titanium oxidized

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