Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Nickel nucleation

The above authors have established that the procedure with the polymeric membrane is not satisfactory. At high current densities, metallic nickel nucleates on the polymeric membrane. Although a reasonable loading of a suspended silica carrier could be achieved, a considerable fraction of the nickel was deposited on the polymeric membrane. The chromia layer method was observed to yield much better results. [Pg.219]

Since the rate of formation of cementite is determined by nucleation, and therefore proceeds more rapidly in fine-grained steels, it follows that the T-T-T diagram will show a more rapid onset of austenite decomposition than in steels of the same composition, but a coarser grain size. The shape of the T-T-T curve is also a function of the steel composition, and is altered by the presence of alloying elements at a low concenuation. This is because the common alloying elements such as manganese, nickel and clrromium decrease... [Pg.187]

Because oxides are usually quite brittle at the temperatures encountered on a turbine blade surface, they can crack, especially when the temperature of the blade changes and differential thermal contraction and expansion stresses are set up between alloy and oxide. These can act as ideal nucleation centres for thermal fatigue cracks and, because oxide layers in nickel alloys are stuck well to the underlying alloy (they would be useless if they were not), the crack can spread into the alloy itself (Fig. 22.3). The properties of the oxide film are thus very important in affecting the fatigue properties of the whole component. [Pg.223]

The carbonyl process developed in 1899 by L. Mond is still used, though it is mainly of historic interest. In this the heated oxide is first reduced by the hydrogen in water gas (H2 + CO). At atmospheric pressure and a temperature around 50°C, the impure nickel is then reacted with the residual CO to give the volatile Ni(CO)4. This is passed over nucleating pellets of pure nickel at a temperature of 230°C when it decomposes, depositing nickel of 99.95% purity and leaving CO to be recycled. [Pg.1146]

Martensitic phase transformations are discussed for the last hundred years without loss of actuality. A concise definition of these structural phase transformations has been given by G.B. Olson stating that martensite is a diffusionless, lattice distortive, shear dominant transformation by nucleation and growth . In this work we present ab initio zero temperature calculations for two model systems, FeaNi and CuZn close in concentration to the martensitic region. Iron-nickel is a typical representative of the ferrous alloys with fee bet transition whereas the copper-zink alloy undergoes a transformation from the open to close packed structure. ... [Pg.213]

Steels and stainless steels show preferential nucleation of pits at inclusions, most notably sulphide inclusions ". Other sulphur-rich regions in ferrous and nickel-based alloys may also lead to premature failure. It has been shown that accumulation of sulphur on the surface of these materials retards passivity and enhances dissolution of the metal. These effects occur in any solution in which the metal shows an active region and they are also preferential pitting sites in the presence of chloride. A recent notion for... [Pg.145]

Where particulate matter (in the form of corrosion products of iron oxide) is present in returning condensate, it often contains copper, nickel, and zinc oxides as well. This debris can initiate foaming (through steam bubble nucleation mechanisms) leading to carryover. It certainly contributes to boiler surface deposits, and the Cu usually also leads to copper-induced corrosion of steel. [Pg.231]

There have been many instances of examination of the effect of additive product on the initiation of nucleation and growth processes. In early work on the dehydration of crystalline hydrates, reaction was initiated on all surfaces by rubbing with the anhydrous material [400]. An interesting application of the opposite effect was used by Franklin and Flanagan [62] to inhibit reaction at selected crystal faces of uranyl nitrate hexa-hydrate by coating with an impermeable material. In other reactions, the product does not so readily interact with reactant surfaces, e.g. nickel metal (having oxidized boundaries) does not detectably catalyze the decomposition of nickel formate [222],... [Pg.36]

The a—time curves for the oxidation reactions [60] of both nickel maleate (534—568 K) and nickel fumarate (548—583 K) were similar to those characteristic of each reactant in vacuum, though E values were reduced to 150 10 kJ mole-1. It was concluded that the distributions of nucleation sites and subsequent patterns of product development were little altered by the change in composition of product from Ni/C (and Ni3C) to NiO. This difference, however, significantly changed the temperature coefficient and stoichiometry of the interface processes, since all carbonaceous material in the reactants was converted to CO2. A constant value of E (150 kJ mole-1) was thus found for the oxidations of the four nickel salts studied [60], the maleate, fumarate, formate and malonate. [Pg.227]

Sigmoid curves, attributable to nucleation and growth reactions, were observed for the decompositions of cobalt phthalate and silver mellitate these are marked in Table 16. The decomposition of nickel terephthalate [88] obeys the Avrami—Erofe ev equation [eqn. (6)], for which n is 1.0— 1.5 and E = 226 8 kJ mole-1. Decompositions of Co—Ni mixed mellitates are discussed in Sect. 7. [Pg.228]

Although some progress has been made in determining the geometry of interface advance through interpretation of observed f(a)—time relationships for individual salts, the reasons for differences between related substances have not always been established. Nickel carboxylates, for which the most extensive sequence of comparative rate studies has been made [40,88,375,502,1106,1107,1109], show a wide variety of kinetic characteristics, but the controlling factors have not yet been satisfactorily determined. Separate measurements of the rates of nucleation and of growth are not usually practicable. [Pg.229]

Figure 5.5. Electron micrographs of different types of diamond film grown on silicon. The white bar shows the scale in micrometres (p.m) (thousandths of a millimetre), (a) The initial stages of diamond growth on a nickel substrate, showing individual diamond crystallites nucleating in scratches and crevices created on the surface by mechanical abrasion, (b) a randomly oriented him,... Figure 5.5. Electron micrographs of different types of diamond film grown on silicon. The white bar shows the scale in micrometres (p.m) (thousandths of a millimetre), (a) The initial stages of diamond growth on a nickel substrate, showing individual diamond crystallites nucleating in scratches and crevices created on the surface by mechanical abrasion, (b) a randomly oriented him,...
Figure 2.26 Heat transfer characteristics for stable nucleate boiling of sodium on a polished, flat, horizontal, nickel plate containing a single cylindrical artificial cavity. (From Deane Rohsenow, 1969. Copyright 1969 by American Society of Mechanical Engineers, New York. Reprinted with permission.)... Figure 2.26 Heat transfer characteristics for stable nucleate boiling of sodium on a polished, flat, horizontal, nickel plate containing a single cylindrical artificial cavity. (From Deane Rohsenow, 1969. Copyright 1969 by American Society of Mechanical Engineers, New York. Reprinted with permission.)...

See other pages where Nickel nucleation is mentioned: [Pg.321]    [Pg.338]    [Pg.14]    [Pg.15]    [Pg.66]    [Pg.72]    [Pg.2452]    [Pg.761]    [Pg.301]    [Pg.330]    [Pg.124]    [Pg.146]    [Pg.275]    [Pg.769]    [Pg.1045]    [Pg.1061]    [Pg.15]    [Pg.84]    [Pg.85]    [Pg.209]    [Pg.212]    [Pg.221]    [Pg.226]    [Pg.229]    [Pg.285]    [Pg.773]    [Pg.775]    [Pg.198]    [Pg.498]    [Pg.104]    [Pg.104]    [Pg.110]   
See also in sourсe #XX -- [ Pg.366 ]




SEARCH



Nickel formate, decomposition nucleation

© 2024 chempedia.info