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Oxide layer thickness

Distance liquid and gas ports 3 mm Silicon oxide layer thickness 200-500 pm... [Pg.584]

The character of the oxide layers influences the kinetics and mechanism of the electrochemical reactions occurring on the platinum anode surface. The relation between the rate of oxygen evolution and oxide layer thickness is complex. In the region where the a-oxides exist, the reaction rate decreases with increasing oxide layer thickness. In the region where the P-oxides exist, the reaction rate depends little on oxide layer thickness or, according to some data, increases with increasing oxide layer thickness. [Pg.546]

Substituting this in Eq. (35), the rate of growth of the oxide is seen to be constant, i.e., the oxide layer thickness increases linearly with time. [Pg.418]

The oxide layer thickness can be determined in a number of ways. Direct microscopic observation has been demonstrated by Takahashi et aV9 Results of other methods can be made to agree... [Pg.426]

The depth profiling technique used on samples with a barrier film before and after the addition of chloride to the buffering borate electrolyte showed no indication of either chloride penetration or significant reduction of the average oxide layer thickness.123 This, of course, does not rule out the possibility of the formation, by any of the mechanisms suggested above, of pinholes with radii much smaller than that of the ion-gun beam, through which the entire active dissolution could take place, or the possibility that the beam missed pits formed sporadically across the surface. If pinholes which are not visible were formed, the dissolution should proceed in them with extremely high true current densities. [Pg.442]

Experiments done in the absence of an external stress showed that the effects of degradation crosslinking are significant at relatively short times of UV exposure, and confirmed that the photodegradation is essentially in the surface layers. The oxidized layer thickness appeared to remain more or less constant after a certain exposure. [Pg.263]

Cluster Efficiency by Erlang s Formula Applied to the Oxide Layer Thickness Problem25... [Pg.293]

FIGURE 7.7 Values of 8/r for several metals where 8 is the oxide layer thickness and r is the radius of a pyrophoric particle, including 8.). [Pg.406]

Figure 8. Tafel plots for the cathodic and anodic current densities for various values of the impurity states of energy E° for an oxide layer thickness of 20 A. (Reprinted from Ref 53.)... Figure 8. Tafel plots for the cathodic and anodic current densities for various values of the impurity states of energy E° for an oxide layer thickness of 20 A. (Reprinted from Ref 53.)...
In P", (a), the oxide packing arrangement comprises close packed layers in a cubic close packed,. .. ABC. .., stacking sequence, which continues throughout the structure. The spinel blocks are four oxide layers thick and contain AP" ions (and stabilising Li, Mg ions) distributed over tetrahedral and octahedral sites, as in spinel, MgAl204. These sites... [Pg.26]

Film Thickness, nm Film Roughness, nm Oxide Layer Thickness, nm Oxide Layer Roughness, nm... [Pg.210]

Fig. 7. Schematic representation of charged cation interstitial (ci) and anion interstitial (ai) bulk concentration profiles within the oxide, leading to defect currents of cation and anion interstitials and subsequent chemical reaction leading to a continual increase in oxide layer thickness, L, with time, t. Fig. 7. Schematic representation of charged cation interstitial (ci) and anion interstitial (ai) bulk concentration profiles within the oxide, leading to defect currents of cation and anion interstitials and subsequent chemical reaction leading to a continual increase in oxide layer thickness, L, with time, t.
Our conclusions thus are that whenever the boundary concentrations C(0) and C(L) are fixed in value by the interfacial reactions, the current is inversely proportional to L and the concentration is a linear function of the position x within the oxide. Considering xjL to be a dimensionless normalized position within the oxide, we can conclude further that the defect concentration is a linear function of this normalized position. It requires only a few more easy steps (cf. Sect. 1.13) to show that the corresponding oxide layer thickness would increase as the square root of the time under these conditions. [Pg.48]

Enumerated Parabolic Law (i.e., rate of oxidation of metal decreases as oxide layer thickness increases)... [Pg.7]

Schultze and Vetter (257) investigated the influence of oxide layer thickness and temperature on the OER overpotential. Following the Gurney-Gerischer theory of charge transfer (252, 253) and assuming the following reaction sequence ... [Pg.84]

R. Williams. A.M. Goodman, Appt Phys. Lett 25 (1974) 531 SD (a) before oxidation, (b) after oxidation till oxide layer thickness > 3 nm. [Pg.734]

As substrate for the sample preparation, silicon wafers from Wacker Chemie AG (Munich, Germany) with a natural silicon oxide layer (thickness 3.8 nm) and a surface roughness of 0.3 nm is used. The wafers are split into small pieces of about 1x1 cm. The pieces are cleaned in a bath sonicator for 20 min in CHCl they are dried in a atmosphere. [Pg.89]

This is a combined organic-inorganic membrane that comprises a macropor-ous a-alumina substrate (tubular or multichannel), an intermediate mesopor-ous inorganic titanium oxide layer (thickness 1 pm) and a microporous Nafion polymer top-layer (thickness less than 0.1 pm). The overall performance and... [Pg.606]

Figure 5. Internal oxidation after oxidation at 1200°C in Nb-20Ti-llSi-5Ge-6Cr-3Fe-2.5Al-2Hf-1.3Sn in (a) cast and heat-treated alloy and (b) in P/M processed alloy. Notice the preferential oxidation of 3 and the interface in relation to the Nb5Si3 phase clear in (a). Oxide layer thickness in (a) was > 100pm and was lost during polishing. Figure 5. Internal oxidation after oxidation at 1200°C in Nb-20Ti-llSi-5Ge-6Cr-3Fe-2.5Al-2Hf-1.3Sn in (a) cast and heat-treated alloy and (b) in P/M processed alloy. Notice the preferential oxidation of 3 and the interface in relation to the Nb5Si3 phase clear in (a). Oxide layer thickness in (a) was > 100pm and was lost during polishing.
Table I Etched thickness and oxidized layer thickness as a function of the rotation speed (treatment during 4 min). Table I Etched thickness and oxidized layer thickness as a function of the rotation speed (treatment during 4 min).
Stirring Rotation Speed rot/min Etched Thickness nm Oxide Layer Thickness nm... [Pg.387]

The results show that for all rotation speeds the etched thickness is higher than the oxide layer thickness. For speeds higher than 168 rot/min the thickness of the oxide layer is not homogeneous and it does not stick. The combination of etching and oxide growth during the same process step allows to perform in the same time decontamination of the surface and growth of the passivation layer. [Pg.387]


See other pages where Oxide layer thickness is mentioned: [Pg.2752]    [Pg.81]    [Pg.520]    [Pg.479]    [Pg.426]    [Pg.148]    [Pg.212]    [Pg.321]    [Pg.291]    [Pg.323]    [Pg.28]    [Pg.288]    [Pg.80]    [Pg.95]    [Pg.267]    [Pg.169]    [Pg.246]    [Pg.81]    [Pg.25]    [Pg.201]    [Pg.298]    [Pg.148]    [Pg.52]    [Pg.267]    [Pg.234]    [Pg.236]   
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