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Metal location

Apart from the instruments described in previous paragraphs, there are others that, while not directly connected with cathodic protection as such, are extremely useful tools to a corrosion engineer. They include pH meters. Redox probes, protective-coating test instruments and buried-metal-location instruments. [Pg.255]

Cinnamaldehyde on Pt/Carbon Catalysts The Effects of Metal Location, and Dispersion on... [Pg.71]

This technology has broad applicability. For instance, using the same carbon support, test results show that a new Pt/C catalyst with edge-metal location and low dispersion resulted in 36% more activity than ESCAT 20 in a standard nitrobenzene (SNB) test (Figure 6). Using the same technology with a different carbon support yielded a catalyst with 57% more activity than ESCAT 20 in SNB test (16,17). [Pg.119]

Catalyst Condition/ Metal Location Dispersion, (%) / metal crystallite Size(nm) Reaction Time (hours) Product Distribution% ... [Pg.501]

Figure 1 Effect of Pd metal location and oxidation state on reaction rate. Figure 1 Effect of Pd metal location and oxidation state on reaction rate.
These six metals located beneath the iron triad on the periodic chart are very much alike. The first three are called the light platinum triad. The heavy platinum triad includes the other two and platinum itself. They are usually found together in nature and are used for similar things. All are shiny and beautiful and they do not tarnish or rust. [Pg.54]

Gold is classed as a heavy, noble metal located just below copper and silver in group 11 of the periodic table. Gold is a good conductor of electricity as well as an excellent heat reflector of infrared radiation, which makes it an efircient thin coating on glass in skyscrapers to reflect the heat of sunhght. [Pg.166]

Tin is a soft, silvery-white metal located in the carbon group, similar in appearance to ftesh-cut aluminum. When polished, it takes on a bluish tint caused by a thin protective coating of oxidi2ed tin. This property makes it useful as a coating for other metals, ft is malleable and ductile, meaning it can be pounded, rolled, and formed into many shapes, as well as pulled into wites through a die. [Pg.201]

Metal location is but one of a number of applications for scanning electron microscope studies in catalysis. Other applications are the study of the morphology of platinum-rhodium gauzes used in the oxidation of ammonia and the poisoning of catalysts, in which the scanning electron microscope results show the location of poisons such as compounds containing sulfur, phosphorus, heavy metals, or coke relative to the location of the catalytic components. [Pg.114]

Metals frequently used as catalysts are Fe, Ru, Pt, Pd, Ni, Ag, Cu, W, Mn, and Cr and some of their alloys and intermetallic compounds, such as Pt-Ir, Pt-Re, and Pt-Sn [5], These metals are applied as catalysts because of their ability to chemisorb atoms, given an important function of these metals is to atomize molecules, such as H2, 02, N2, and CO, and supply the produced atoms to other reactants and reaction intermediates [3], The heat of chemisorption in transition metals increases from right to left in the periodic table. Consequently, since the catalytic activity of metallic catalysts is connected with their ability to chemisorb atoms, the catalytic activity should increase from right to left [4], A Balandin volcano plot (see Figure 2.7) [3] indicates apeak of maximum catalytic activity for metals located in the middle of the periodic table. This effect occurs because of the action of two competing effects. On the one hand, the increase of the catalytic activity with the heat of chemisorption, and on the other the increase of the time of residence of a molecule on the surface because of the increase of the adsorption energy, decrease the catalytic activity since the desorption of these molecules is necessary to liberate the active sites and continue the catalytic process. As a result of the action of both effects, the catalytic activity has a peak (see Figure 2.7). [Pg.429]

Two commercially important species of Louisiana crayfish, Procambarus clarkii and P. acutus, from the Atchafalaya River Basin, from open ponds, and from the sediment and water of these environments, were sampled three times during two consecutive fishing (production) seasons [19]. The abdominal muscle and hepatopancreatic tissue were analyzed separately. Lead, Hg, and Cd, if present, were in concentrations below the limit of detection (LoD). The heptato-pancreatic tissue contained (in p,gkg 1) Ba<8, Cu 11-15, and Fe < 640. Abdominal muscle samples had <3 p,gkg 1 of most metals. Locations with the highest levels of metal residues in sediment were not necessarily locations where crayfish had the highest levels in their tissues. [Pg.444]

Fe(ni)/Fe(II), Ag(I)/Ag(0), and Hg(II)/Hg(0). Figure 1 reports the reduction potential of different metals compared with both the valence band potential and the conduction band potential. All metals located above the conduction band can theoretically be reduced (Chen and Ray, 2001). [Pg.72]

Another series of related mesomorphic metallodendrimers, having the metal located at the core of the dendrimer, were also reported [285]. The dendritic ligands were obtained by condensation of the corresponding 1,3-dione with aminopropanol, and the dicopper complexes were then formed by the reaction with copper(ii) acetate (Fig. 60). These Ugands, also based on the first generation Frechet-Percec dendron motif, were not themselves mesomorphic, but upon complexation, mesophases were observed whose sta-... [Pg.119]

Figure 9 Hydrocarbon emissions in the ECE/EUDC test from a 1.2-liter-enginc vehicle fitted with catalysts containing different platinum-group metals located under the floor. Figure 9 Hydrocarbon emissions in the ECE/EUDC test from a 1.2-liter-enginc vehicle fitted with catalysts containing different platinum-group metals located under the floor.
Figure 2. Ribbon diagram of the ASV IN catalytic domain, with explicitly shown active site side chains for both Zn (black) and Mn (grey) complexes. The metal locations and corresponding coordinated water molecules are indicated in the same colors. Figure 2. Ribbon diagram of the ASV IN catalytic domain, with explicitly shown active site side chains for both Zn (black) and Mn (grey) complexes. The metal locations and corresponding coordinated water molecules are indicated in the same colors.
The metals/semi-metals located at the foot of groups IIIA, IVA and VA have several features in common large metallic radii and low surface energies (see table 1). [Pg.333]

A way to limit the direct ligand chemical effect is to associate metals located close together in the periodic table, i.e. having similar electronic... [Pg.405]


See other pages where Metal location is mentioned: [Pg.339]    [Pg.256]    [Pg.535]    [Pg.72]    [Pg.74]    [Pg.270]    [Pg.39]    [Pg.211]    [Pg.614]    [Pg.129]    [Pg.183]    [Pg.114]    [Pg.429]    [Pg.67]    [Pg.3]    [Pg.279]    [Pg.72]    [Pg.74]    [Pg.73]    [Pg.50]    [Pg.73]   
See also in sourсe #XX -- [ Pg.297 , Pg.298 , Pg.299 , Pg.300 , Pg.301 , Pg.302 , Pg.303 , Pg.304 , Pg.305 , Pg.306 , Pg.307 , Pg.308 , Pg.309 ]




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