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Thin metallic alloys

Thin films of metals, alloys and compounds of a few micrometres diickness, which play an important part in microelectronics, can be prepared by die condensation of atomic species on an inert substrate from a gaseous phase. The source of die atoms is, in die simplest circumstances, a sample of die collision-free evaporated beam originating from an elemental substance, or a number of elementary substances, which is formed in vacuum. The condensing surface is selected and held at a pre-determined temperature, so as to affect die crystallographic form of die condensate. If diis surface is at room teiiiperamre, a polycrystalline film is usually formed. As die temperature of die surface is increased die deposit crystal size increases, and can be made practically monocrystalline at elevated temperatures. The degree of crystallinity which has been achieved can be determined by electron diffraction, while odier properties such as surface morphology and dislocation sttiicmre can be established by electron microscopy. [Pg.3]

It was quite recently reported that La can be electrodeposited from chloroaluminate ionic liquids [25]. Whereas only AlLa alloys can be obtained from the pure liquid, the addition of excess LiCl and small quantities of thionyl chloride (SOCI2) to a LaCl3-sat-urated melt allows the deposition of elemental La, but the electrodissolution seems to be somewhat Idnetically hindered. This result could perhaps be interesting for coating purposes, as elemental La can normally only be deposited in high-temperature molten salts, which require much more difficult experimental or technical conditions. Furthermore, La and Ce electrodeposition would be important, as their oxides have interesting catalytic activity as, for instance, oxidation catalysts. A controlled deposition of thin metal layers followed by selective oxidation could perhaps produce cat-alytically active thin layers interesting for fuel cells or waste gas treatment. [Pg.300]

Typical marine propellers are fixed pitch and small in diameter with veiy thin, but broad, blade sections. They are made from either cast metal, corrosion-resistant metal alloys such as copper, or composite materials. Marine propellers normally operate at 60 percent efficiency due to the proximity of the ship s hull, which limits the overall diameter of the propeller and disturbs the efficient flow of water through the blades. As a result, the blades have to be veiy wide to produce adequate thrust. Marine propeller designers use innovations such as overlapping blades and wheel vanes to offset those problems and improve efficiency. [Pg.957]

P. Mazzoldi, G. Mattel, C. Maurizio, E. Cattaruzza, F. Gonella, in E. Knystautas (ed.) Metal Alloy Nanoclusters by Ion Implantation in Silica, in Engineering Thin Films and Nanostructures with Ion Beams, Chapter 7, CRC Press, New York, 2005, 82. [Pg.289]

Environmental tests have been combined with conventional electrochemical measurements by Smallen et al. [131] and by Novotny and Staud [132], The first electrochemical tests on CoCr thin-film alloys were published by Wang et al. [133]. Kobayashi et al. [134] reported electrochemical data coupled with surface analysis of anodically oxidized amorphous CoX alloys, with X = Ta, Nb, Ti or Zr. Brusic et al. [125] presented potentiodynamic polarization curves obtained on electroless CoP and sputtered Co, CoNi, CoTi, and CoCr in distilled water. The results indicate that the thin-film alloys behave similarly to the bulk materials [133], The protective film is less than 5 nm thick [127] and rich in a passivating metal oxide, such as chromium oxide [133, 134], Such an oxide forms preferentially if the Cr content in the alloy is, depending on the author, above 10% [130], 14% [131], 16% [127], or 17% [133], It is thought to stabilize the non-passivating cobalt oxides [123], Once covered by stable oxide, the alloy surface shows much higher corrosion potential and lower corrosion rate than Co, i.e. it shows more noble behavior [125]. [Pg.274]

Basically, three kinds of membranes are being studied inorganic oxide membranes, polymer-based membranes, and metal and metal alloy membranes. Some combinations of these are also used, such as impregnating inorganic oxide membranes with catalytic materials. A key term in this held is permselective membrane, which is a thin material that can allow a certain component of a mixture, but not other components, to pass through (or permeate) from one side to the other. [Pg.84]

The use of EM (except in the special case of SEM) demands that the catalyst, whether mono-or multi-phasic, be thin enough to be electron transparent. But, as we show below, this seemingly severe condition by no means restricts its applicability to the study of metals, alloys, oxides, sulfides, halides, carbons, and a wide variety of other materials. Most catalyst powder preparations and supported metallic catalysts, provided that representative thin regions are selected for characterization, are found to be electron transparent and thus amenable to study by EM without the need for further sample preparation. [Pg.198]

Gasgnier, M. (1995) The intricate world of rare erath thin films metals, alloys, intermetallics, chemical compounds. In Handbook on the Physics and Chemistry of Rare Earths, eds. Gschneidner. Jr., K.A. and Eyring, L. (Elsevier, Amsterdam, The Netherlands), Vol. 20, p. 105. [Pg.612]

When the powder is isostatically compacted at elevated temperatnres, the process is called hot isostatic pressing (HIP). In this case, the flexible dies are often made of thin metals, and high-pressnre gases snch as argon are nsed to heat the part rapidly and rednce thermal losses. Pressnre np to 100 MPa and temperatnres in excess of 2000°C are possible nsing HIP, and parts up to 600 kg can be fabricated. A schematic diagram of a typical HIP apparatus is shown in Figure 7.18. Metals that are processed commercially by HIP include various specialty steels, superalloys, hard metals, refractory alloys, and beryllium. We will see in Section 7.2 that HIP is also particularly useful for the densification of ceramic components. [Pg.703]


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