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Surface blocking

The geometric factor can be illustrated by considering the amount of sunlight (or radiative heat) received by Earth from the Sun. If you draw a huge sphere with a radius of 150 million km (93 million miles) around the sun that passes through Earth, the geometric factor for the Sun to Earth would he the ratio of the area on that sphere s surface blocked by Earth to the surface area of the sphere. Obviously, Earth receives only a tiny fraction of the total energy emitted from the Sun. [Pg.613]

Optimum conditions for the formation of CdS by the acidic method on metallic A1 substrate at 25 °C have been reported as follows pH 2.3, potential -1 V vs. SCE, and electrolysis time > 2 h [44]. Thermal treatment improved the characteristics of the films and their photovoltaic properties, which were evaluated by evaporating a CU2S layer on the CdS/Al film, to form a heterojunction cell. The influence of the deposition substrate on the formation and morphology of CdS was found to be important. The aluminum substrates gave the best results among Pt, Mo, and Al. In the case of molybdenum, surface blocking by adsorbed sulfur was considered. [Pg.92]

As shown in the reaction Scheme (6.16), the reaction that yields the poisoning intermediate is a chemical reaction, and no electrons are implied in the process. Additionally, the reaction takes place at open circuit, i.e., without potential control. This property has been used to measure the total amount of poisoning intermediate that can be accumulated on the surface. The amount and fraction of the surface blocked... [Pg.180]

This would be consistent with a transformation of a COad-rich (2 x 2)(2CO + O) adsorbate phase [Schiffer et al., 1997] into an oxygen-rich, but stiU COad-containing phase, for example the (2 x 2)(CO + 20) phase known from UHV experiments [Narloch et al., 1994], CO adsorption on the Ru(OOOl) surface at 0.7 V is essentially inhibited [Wang et al., 2001], most likely as a result of surface blocking by OHad/ Oad species. [Pg.486]

Because of the lower adsorption energies on the Pt monolayer islands, the steady-state coverage on the islands is relatively low, and surface blocking plays no role. [Pg.491]

The first aspect of biocompatibility is a natural immune response. When a foreign object enters the blood stream, it can be attacked by the body s defense system. The first step is protein adsorption on an object surface. It is believed that the amount and type of protein adsorption is one of the most important steps determining whether the object is tolerated or rejected by the body. The next step is cell adhesion, which may cause aggregation and activation of platelets and triggering of the blood coagulation system with resulting thrombus formation. It may not only lead to sensor failure via surface blocking but directly threatens the patient s health. [Pg.126]

The phosphate backbone of DNA molecules often results in undesirable electrostatic interactions with the substrate. Although the electrostatic interactions of DNA can be utilized for physical adsorption of DNA to the surface, this process can also lead to the nonspecific physical adsorption of target DNA on the surface. Rather than sample DNA hybridizing to the probe, it can adsorb to the surface and lead to interferences with the final detection call. Nonspecific adsorption effects have primarily been examined by the microarray community. Blocking strategies have been developed to prevent these nonspecific interactions. Succinic anhydride (SA) and bovine serum albumin (BSA) are two common methods to prevent nonspecific adsorption on amine modified surfaces. Blocking strategies are desired to react with or pas-... [Pg.173]

Kaolinite is easily cleaved perpendicular to the c direction, since the interactions between the aluminosilicate layers are much weaker than the intralayer interactions. Therefore as a part of this work the structure and surface energy, of the resulting 001 surface are considered. The surface energy may be evaluated from the energy of a single layer surface block of clay in a vacuum, U, and the energy of a portion of the bulk clay, U, containing the same number of atoms as the surface block. [Pg.91]

Rogozhnikov [95] has analyzed the impedance response of an Ag electrode in cyanide solutions. The impedance spectra have shown time evolution of the surface blocking. Time evolution of the active Ag electrode area after immersion in CN containing solutions has been analyzed by Baltrunas et al. [96]. A time of20-60 s was required for settling down the blocking (dependent also on CN concentration). [Pg.924]

EXAMPLE 13.6 An Entropic Model for Steric Stabilization Due to Adsorbed Polymer Layers. Picture a flat surface to which rigid rods are attached by ball-and-socket-type joints. The free ends of the rods can lie anywhere on the surface of a hemisphere. The approach of a second surface blocks access to some of the sites on the cap of the hemisphere. Outline the qualitative argument that converts this physical picture to a theory for stabilization. What are some of the shortcomings of the model ... [Pg.619]

In the case of surface-block dendrimers, the dendrimer periphery exhibits different functionalities in specific molecular segments. They are formed by coupling of dendrons differing in the nature of their terminal functionalities to a common core unit (cf. Section 3.2.1) [6, 10]. [Pg.28]

Phosphorus-containing surface-block dendrimers can be prepared by a method developed by Majoral et al. [57] (Fig. 3.9). [Pg.62]

Fig. 3.8 Convergent synthesis of a bifunctionalised dendrimer with two different peripheral groups in separate molecular segments (surface-block dendrimers)... Fig. 3.8 Convergent synthesis of a bifunctionalised dendrimer with two different peripheral groups in separate molecular segments (surface-block dendrimers)...
Surface-block dendrimer with different peripheral groups in separate segments of the molecule. [Pg.72]

Figure 3.2 Operation of the scanning electrochemical microscope illustrating diffusion of a redox mediator to the microscope tip (a) when the tip is far from any surface (b) when the tip is near an insulator and the insulating surface blocks transport of the mediator to the tip (c) when the tip is near a conducting surface that regenerates the mediator, this causing an enhanced current... Figure 3.2 Operation of the scanning electrochemical microscope illustrating diffusion of a redox mediator to the microscope tip (a) when the tip is far from any surface (b) when the tip is near an insulator and the insulating surface blocks transport of the mediator to the tip (c) when the tip is near a conducting surface that regenerates the mediator, this causing an enhanced current...
Chiche et a/.[56] have studied the oligomerization of butene over a series of zeolite (HBeta and HZSM-5), amorphous silica alumina and mesoporous MTS-type aluminosilicates with different pores. The authors found that MTS catalyst converts selectively butenes into a mixture of branched dimers at 423 K and 1.5-2 MPa. Under the same reaction conditions, acid zeolites and amorphous silica alumina are practically inactive due to rapid deactivation caused by the accumulation of hydrocarbon residue on the catalyst surface blocking pores and active sites. The catalytic behaviour observed for the MTS catalyst was attributed to the low density of sites on their surface along with the absence of diffusional limitations due to an open porosity. This would result in a low concentration of reactive species on the surface with short residence times, and favour deprotonation and desorption of the octyl cations, thus preventing secondary reaction of the olefinic products. [Pg.132]

These apparent discrepancies can be resolved as follows. First, the values at lower temperatures (S/Nis = 0.25 and 0.33) (96, 104, 111) are smaller because hydrogen atoms from the dissociative chemisorption of H2S remain adsorbed on the nickel surface blocking sites for further sulfur adsorption. At higher temperatures hydrogen desorbs allowing sulfur atoms to cover most or all of the nickel sites, and thus higher S/Nis ratios (e.g., 0.6-0.7) are observed. [Pg.160]

Figure 17 Schematic of an idealized corrosion product deposit on a corroding surface l is the pore length, eA the fracture of the surface area exposed to the corrosion environment (1 — eA) is the fraction of the surface blocked by corrosion product deposit. Figure 17 Schematic of an idealized corrosion product deposit on a corroding surface l is the pore length, eA the fracture of the surface area exposed to the corrosion environment (1 — eA) is the fraction of the surface blocked by corrosion product deposit.

See other pages where Surface blocking is mentioned: [Pg.56]    [Pg.603]    [Pg.385]    [Pg.181]    [Pg.284]    [Pg.429]    [Pg.432]    [Pg.491]    [Pg.494]    [Pg.558]    [Pg.477]    [Pg.95]    [Pg.187]    [Pg.339]    [Pg.164]    [Pg.489]    [Pg.146]    [Pg.77]    [Pg.365]    [Pg.312]    [Pg.62]    [Pg.62]    [Pg.40]    [Pg.210]    [Pg.81]    [Pg.444]    [Pg.327]    [Pg.315]    [Pg.217]    [Pg.2]   
See also in sourсe #XX -- [ Pg.229 ]




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Block copolymer thin film surface

Block copolymers (cont surface behavior of films

Block copolymers surface energies

Block surface morphology

Copolymer, block surface-induced ordering

Dendrimer surface-block

Dendritic block copolymers surface

Electron transfer at surfaces through a blocking layer

Partially blocked surface

Surface Energies of the Block Copolymers

Surface blocking agents

Surface forces from amphiphilic block copolymers

Surface instability of compressed or bent blocks

Surface properties block copolymers

Surface three-block copolymer

Surface treatments styrene block copolymers

Surface-block copolymers

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