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Alloys containing palladium

In dentistry, palladium alloys are widely used as alternatives to base metal alloys in the manufacture of crowns and bridges as weU as the replacement of lost or damaged teeth (see Dental materials). Such alloys contain over 80% palladium, and hence offer significant cost benefits over alloys containing a high proportion of gold. [Pg.174]

The corrosion behaviour of amorphous alloys has received particular attention since the extraordinarily high corrosion resistance of amorphous iron-chromium-metalloid alloys was reported. The majority of amorphous ferrous alloys contain large amounts of metalloids. The corrosion rate of amorphous iron-metalloid alloys decreases with the addition of most second metallic elements such as titanium, zirconium, vanadium, niobium, tantalum, chromium, molybdenum, tungsten, cobalt, nickel, copper, ruthenium, rhodium, palladium, iridium and platinum . The addition of chromium is particularly effective. For instance amorphous Fe-8Cr-13P-7C alloy passivates spontaneously even in 2 N HCl at ambient temperature ". (The number denoting the concentration of an alloy element in the amorphous alloy formulae is the atomic percent unless otherwise stated.)... [Pg.633]

The addition of beryllium and silicon to nickel-palladium alloys gives very good high-temperature brazes, especially for alloys containing aluminium and titanium. [Pg.937]

We have, then, another example of an alloy and reaction in which the simple d-band theory has to be modified in a rather speculative way in order to explain experimental results. Actually, this is unnecessary for the formic acid reaction if we take the more recent value of about 0.4 for the number of d-band holes per palladium atom. This is not a satisfactory solution, because it is then difficult to explain the low activation energy for the parahydrogen conversion on Pd-Au alloys containing between 40 and 60% Pd. [Pg.161]

Mishchenko, A. P. and M. E. Sarylova. 1981. Hydrogen permeability and catalytic activity of a membrane catalyst from a palladium alloy containing 6% ruthenium in relation to hydrogenation of 1,3-pcntadicnc. Met. i Splavy Membrane Kak. Katalyz. M. 75-81. [Pg.146]

H. Palladium. Palladium (mp 1,SS2°C), is soft and ductile but work-hardens. At elevated temperatures, the diffusion of hydrogen through palladium is rapid, which forms the basis of a method for the purification of hydrogen. The best performance is obtained from a palladium-silver alloy containing about 18% silver because, unlike pure Pd, this alloy does not undergo a phase transition in the presence of hydrogen. Palladium is not as inert as platinum and is attacked by sulfuric and nitric acids. [Pg.312]

Silver and gold have an interesting influence. Addition of silver to palladium at first increases the solubility of hydrogen despite the fact that hydrogen is insoluble in pure silver. The maximum solubility is reached with 40 per cent, of silver, after which it falls. At 138° C. an alloy containing 40 per cent, of silver and 60 per cent, of palladium absorbs four times as much hydrogen as pure palladium. With 70 per cent, of silver the solubility of hydrogen is reduced to zero. [Pg.179]

With gold, palladium likewise yields no compounds, the freezing-point curve falling continuously, and lying concave to the axis of concentration. The hardness of the alloys increases up to 70 per cent, of palladium and then decreases. Alloys containing more than 10 per cent, of palladium are white.3... [Pg.192]

Alloys of palladium and gold, containing from 60 to 90 per cent, of the latter metal, are known as rhotanium, and, on account of their high melting-point, strength, and incorrodibility, have been recommended as substitutes for platinum. [Pg.192]

An alloy containing 5 parts by weight of palladium and 4 of silver was found by Graham3 to be still capable of absorbing hydrogen. [Pg.193]

Palladium silver alloys admit of receiving a high polish, and retain their bright surface. An alloy containing 38 per cent, of palladium, the remainder being silver, was formerly used for dental purposes. [Pg.193]

Interesting support to the belief that the compound Pd2Pb can exist is afforded by the results of experiments 5 to determine the difference of potential between various alloys and pure lead in a normal solution of lead nitrate. The alloys were prepared by melting the palladium and lead under a mixture of lithium chloride and either potassium or barium chloride. Alloys containing less than 33 per cent, of palladium have a potential practically identical with that of pure lead, whilst those containing more than this amount of palladium exhibit a higher potential, which at first rapidly increases with the palladium. Between 20 and 90 per cent, of palladium the alloys are harder than the individual components, a maximum occurring with 65 per cent, of palladium. [Pg.193]

Palladium Monosilicide, PdSi, is obtained as brilliant bluish grey fragments on treating any Pd-Si alloy, containing above 60 per cent, of silicon, with dilute potash. The free silicon dissolves, leaving the silicide as residue. Density 7-31 at 15° C. [Pg.207]

Synthesis of alloyed silver-palladium bimetallic nanoparticles was achieved by /-irradiation of aqueous solutions containing a mixture of Ag and Pd metal ions using different Ag/Pd ratios. The synthesis of alloys implies the simultaneous radio-induced reduction of silver and palladium ions. The nanoparticles were characterized by UV-visible spectroscopy, transmission electron microscopy (TEM) and energy dispersive X-ray spectroscopy (EDS). The Ag-Pd nanoparticles display a face-centered cubic (fee) crystalline structure. The lattice parameter was measured for several Ag/Pd ratios and was found to closely follow Vegard s law, which indicates the formation of homogeneous alloys. In order to avoid the simultaneous reduction of silver and palladium ions which leads to alloyed bimetallic nanoparticles. [Pg.358]

Metal- and alloy-containing membranes are currently applied mainly in ultrapure hydrogen production. Pilot plants with palladium alloy tubular membrane catalyst were used in Moscow for hydrogenation of acetylenic alcohols into ethylenic ones. In the Topchiev Institute of Petrochemical Synthesis, a laboratory-scale reactor of the same type was tested... [Pg.453]

The XRD pattern of the coprecipitated catalyst (PdZr-c, trace 5) show palladium reflections indicating the presence of palladium crystallites, while the reflections due to zirconia phases are greatly broadened, which suggests amorphous phases. XRD line broadening and electron microscopy indicated that the catalysts prepared by oxidation of the glassy alloy were made up of small poorly crystalline palladium domains of about 5-7 nm lateral dimension. These domains were flilly integrated in predominantly amorphous zirconia. Although the coprecipitated catalyst contained palladium particles of about similar size (8 nm). [Pg.288]

A possible solution to avoid this phenomenon is represented by the use of a Pd-alloy containing another metal, such as silver. The role of silver is explained by its electron donating behaviour, being largely similar to the one of the hydrogen atom in palladium. Silver and hydrogen atoms would compete for the filling of electron holes [42]. [Pg.32]

The most important problem associated with the use of pure palladium membranes is the hydrogen embrittlement phenomenon. When the temperature is below 300 °C and the pressure below 2.0 MPa, the 3-hydride phase may nucleate from the a-phase, resulting in severe lattice strains (see Figure 13.3), so that a pure palladium membrane becomes brittle after a few cycles of oc (3 transitions. Such a problem can be overcome by using Pd-alloy containing another metal, such as silver. The palladium alloys have a reduced critical temperature for the oc-P phase transition. Pd-Ag membranes can operate in hydrogen atmosphere at temperatures below 300 °C without observing... [Pg.113]

An alloy contains atoms of more than one element and has the properties of a metal. In a solution alloy the components are randomly dispersed. In a heterogeneous alloy the components are not evenly di rsed and can be distinguished at a macroscopic level In an intermetallic compound the components have interacted to form a compound substance, as in CU3AS 12.39 Statement (b) is false. 12.41 (a) True (b) false (c) false 12.43 (a) Nickel or palladium, substitutional alloy (b) copper, substitutional alloy (c) silver, substitutional alloy 12.45 (a) True (b) false (c) false (d) false... [Pg.1120]


See other pages where Alloys containing palladium is mentioned: [Pg.367]    [Pg.427]    [Pg.367]    [Pg.427]    [Pg.384]    [Pg.127]    [Pg.461]    [Pg.932]    [Pg.160]    [Pg.184]    [Pg.431]    [Pg.691]    [Pg.25]    [Pg.292]    [Pg.384]    [Pg.736]    [Pg.437]    [Pg.97]    [Pg.887]    [Pg.1]    [Pg.305]    [Pg.683]    [Pg.675]    [Pg.324]    [Pg.325]    [Pg.349]    [Pg.350]    [Pg.725]    [Pg.1079]    [Pg.109]    [Pg.84]    [Pg.1489]   
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