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Surface morphologies

In order to classify the various patterns as a function of the laser energy absorbed by the surface, the Laser Intensity Factor (LIF), is defined [11]  [Pg.294]


SEM Scanning electron microscopy [7, 10, 14] A beam of electrons scattered from a surface is focused Surface morphology... [Pg.313]

Annis B K, Noid D W, Sumpter B G, Reffner J R and Wunderlich B 1992 Application of atomic force microscopy (AFM) to a block copolymer and an extended chain polyethylene Makromol. Chem., Rapid. Commun. 13 169 Annis B K, Schwark D W, Reffner J R, Thomas E L and Wunderlich B 1992 Determination of surface morphology of diblock copolymers of styrene and butadiene by atomic force microscopy Makromol. Chem. 193 2589... [Pg.1727]

Detemiining compositions is possible if the distribution of elements over the outer layers of the sample and the surface morphology is known. Two limiting cases are considered, namely a homogeneous composition tliroughout the outer layers and an arrangement in which one element covers the other. [Pg.1855]

Fig. 5. The effect of ultrasonic irradiation on the surface morphology and particle size ofNi powder. Initial particle diameters (a) before ultrasound were i 160 fim-, (b) after ultrasound, fim. High velocity interparticle coUisions caused by ultrasonic irradiation of slurries are responsible for the smoothing... Fig. 5. The effect of ultrasonic irradiation on the surface morphology and particle size ofNi powder. Initial particle diameters (a) before ultrasound were i 160 fim-, (b) after ultrasound, fim. High velocity interparticle coUisions caused by ultrasonic irradiation of slurries are responsible for the smoothing...
Imaging of Surfaces—Analysis of Surface Morphology. Several important techniques can help answer the question what does the surface look like This question is often the first one to be posed ia the characterization of a new surface or iaterface. Physical imaging of the surface is necessary to distinguish the relevant features important for understanding the whole surface and is essential for accurate iaterpretation of data from other surface analysis techniques which might later be appHed to a more limited region of the surface or iaterface. [Pg.270]

Platinum—Iridium. There are two distinct forms of 70/30 wt % platinum—iridium coatings. The first, prepared as prescribed in British patents (3—5), consists of platinum and iridium metal. X-ray diffraction shows shifted Pt peaks and no oxide species. The iridium [7439-88-5] is thus present in its metallic form, either as a separate phase or as a platinum—iridium intermetallic. The surface morphology of a platinum—iridium metal coating shown in Figure 2 is cracked, but not in the regular networked pattern typical of the DSA oxide materials. [Pg.121]

The deposition of ions at the cathode creates a depletion layer across which the ions must migrate in order to deposit. This layer can vary in thickness according to surface morphology. The depletion layer is more or less defined as the region where the ion concentration differs from that of the bulk solution by >1%. The layer thickness can be decreased by agitation. [Pg.527]

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]

Figure 1.3 Surface morphology of AI2 O3 single erystal after evaporation in vaeuo at 2000° C. (a) the basal plane, and (b) a plane normal to the basal plane. Note the formation of ledges on the (0110) plane... Figure 1.3 Surface morphology of AI2 O3 single erystal after evaporation in vaeuo at 2000° C. (a) the basal plane, and (b) a plane normal to the basal plane. Note the formation of ledges on the (0110) plane...
Another example of static SIMS used in a more quantitative role is in the analysis of extmded polymer blends. The morphology of blended polymers processed by extrusion or molding can be affected by the melt temperature, and pressure, etc. The surface morphology can have an effect on the properties of the molded polymer. Adhesion, mechanical properties, and physical appearance are just a few properties affected by processing conditions. [Pg.556]

In a molded polymer blend, the surface morphology results from variations in composition between the surface and the bulk. Static SIMS was used to semiquan-titatively provide information on the surface chemistry on a polycarbonate (PC)/polybutylene terephthalate (PBT) blend. Samples of pure PC, pure PBT, and PC/PBT blends of known composition were prepared and analyzed using static SIMS. Fn ment peaks characteristic of the PC and PBT materials were identified. By measuring the SIMS intensities of these characteristic peaks from the PC/PBT blends, a typical working curve between secondary ion intensity and polymer blend composition was determined. A static SIMS analysis of the extruded surface of a blended polymer was performed. The peak intensities could then be compared with the known samples in the working curve to provide information about the relative amounts of PC and PBT on the actual surface. [Pg.556]

S. Suresh and R. O. Ritchie, A Geometric Model for Fatigue Crack Closure Induced by Fracture Surface Morphology , Metallurgical Transactions, 13A, 1982, pp. 1627 1631. [Pg.533]

A more recent process, the P2 etch [60], which uses ferric sulfate as an oxidizer in place of sodium dichromate avoids the use of toxic chromates, but still provides a similar oxide surface morphology (Fig. 15) allowing a mechanically interlocked interface and strong bonding [9]. The P2 treatment has wide process parameter windows over a broad range of time-temperature-solution concentration conditions and mechanical testing confirms that P2-prepared surfaces are, at a minimum, equivalent to FPL-prepared specimens and only slightly inferior to PAA-prepared surfaces [61]. [Pg.964]

Fig. 1.91 Variation in possible erosion corrosion surface morphology (a) single phase attack of mild steel in water (b) droplet erosion corrosion of 12% Cr steel... Fig. 1.91 Variation in possible erosion corrosion surface morphology (a) single phase attack of mild steel in water (b) droplet erosion corrosion of 12% Cr steel...
Naoi and co-workers [55], with a QCM, studied lithium deposition and dissolution processes in the presence of polymer surfactants in an attempt to obtain the uniform current distribution at the electrode surface and hence smooth surface morphology of the deposited lithium. The polymer surfactants they used were polyethyleneglycol dimethyl ether (molecular weight 446), or a copolymer of dimethylsilicone (ca. 25 wt%) and propylene oxide (ca. 75 wt%) (molecular weight 3000) in LiC104-EC/DMC (3 2, v/v). [Pg.348]


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