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Adsorbents particle

The saturation coverage during chemisorption on a clean transition-metal surface is controlled by the fonnation of a chemical bond at a specific site [5] and not necessarily by the area of the molecule. In addition, in this case, the heat of chemisorption of the first monolayer is substantially higher than for the second and subsequent layers where adsorption is via weaker van der Waals interactions. Chemisorption is often usefLil for measuring the area of a specific component of a multi-component surface, for example, the area of small metal particles adsorbed onto a high-surface-area support [6], but not for measuring the total area of the sample. Surface areas measured using this method are specific to the molecule that chemisorbs on the surface. Carbon monoxide titration is therefore often used to define the number of sites available on a supported metal catalyst. In order to measure the total surface area, adsorbates must be selected that interact relatively weakly with the substrate so that the area occupied by each adsorbent is dominated by intennolecular interactions and the area occupied by each molecule is approximately defined by van der Waals radii. This... [Pg.1869]

If < 1, then binding is anticooperative, for example when an electrically charged particle adsorbs at an initially neutral surface the accumulated charge repels subsequent arrivals and makes their incorjDoration more difficult [58]. [Pg.2825]

Fig. 17. SoHd particles adsorbed at the oil-water iaterface serve as stabilizers for an emulsion. Fig. 17. SoHd particles adsorbed at the oil-water iaterface serve as stabilizers for an emulsion.
The identification of particles adsorbed on solid surfaces and recognition of their properties is one of the fundamental problems in research on adsorption and heterogeneous catalysis. Desorption of the adsorbed species from a surface and its subsequent analysis is an important method for solv-... [Pg.343]

Let us consider a surface on which particles are adsorbed on sites with different activation energy of desorption, and the distribution of these energies over the surface is discrete so that ni0 particles are initially in a state with an activation energy of desorption Edt, n particles with an energy Ed/, etc. Such a model corresponds to a concept of adsorption on different crystal planes each of which is homogeneous, or to a concept of different adsorption states of the particles adsorbed on a single crystal (26, 88). [Pg.381]

Depending on the nature of the system, the adsorption process can be either reversible or irreversible. In the first case an adsorption equilibrium exists between the particles adsorbed on the adsorbent s surface and the particles in the electrolyte (or in any other phase contacting with the adsorbent). After removing the substance from the electrolyte, adsorbed particles leave the surface and reenter into the electrolyte. In the case of an irreversible adsorption, the adsorbed particles remain at the surface even if their concentration in the bulk phase drops to zero. In this case the adsorbed particles can be removed from the surface only by means of a chemical reaction... [Pg.157]

Without sonication, Pt particles adsorb primarily on the external surface of SBA-15 and at the mesopore openings. Sonication promotes homogeneous inclusion and deposition of Pt nanoparticles on the inner surface of the support mesopores, because ca. 90% of the total surface area is from the inner pore walls. Heat treatment... [Pg.154]

Let us start with a definition. Semiconductor chemical sensor is an electronic device designed to monitor the content of particles of a certain gas in surrounding medium. The operational principle of this device is based on transformation of the value of adsorption directly into electrical signal. This signal corresponds to amount of particles adsorbed from surrounding medium or deposited on the surface of operational element of the sensor due to heterogeneous diemical reaction. [Pg.5]

In this example, a simple mechanism for breaking a colloid was chosen. The eggshells are made of porous calcium carbonate, their surface covered with innumerable tiny pores. The particles of fat in the broth accumulate in these small pores. Removing the eggshells from the broth (each with oil particles adsorbed on their surfaces) removes the dispersed medium from the broth. One of the two components of the colloid is removed, preventing the colloid from persisting. [Pg.510]

In air, endrin is expected to be associated primarily with particulate matter, based on its low vapor pressure and high Koc (Kenaga 1980). However, small amounts of endrin in the atmosphere may exist in the vapor phase (Eisenreich et al. 1981). Because of its low solubility (200 pg/L, see Table 3-2), endrin would not be expected to be removed significantly from the atmosphere by wet deposition. Particle-adsorbed endrin will be removed from the atmosphere by both wet and dry deposition. In recent studies in the Great Lakes area, endrin was found in 5% of 450 wet deposition (rain/snow) samples collected between 1986-1991, at volume weighted mean concentrations ranging from 0.02 to 0.98 ng/L (ppt) (Chan et al. 1994). [Pg.115]

Fig. 6-4. Electron energy levels of an adsorbate particle broadened by interaction with adsorbent metal crystal M adsorbent metal R = atomic adsorbate particle = adsorbed particle W= probability density of electron energy states x = distance to adsorbate particle, xq = distance to adsorbed particle. Fig. 6-4. Electron energy levels of an adsorbate particle broadened by interaction with adsorbent metal crystal M adsorbent metal R = atomic adsorbate particle = adsorbed particle W= probability density of electron energy states x = distance to adsorbate particle, xq = distance to adsorbed particle.
Here, is the mean streaming velocity of particles approaching the wall and (1 — a) is the fraction of fluid particles reflected at the wall, so the first term represents the distribution of particles adsorbed. The velocity distribution functions, /(v), are assumed to be Maxwellian,... [Pg.81]

Figure 4.6. Definition of the contact angle 0 for a particle adsorbed at the water-oil interface. Case where the particle is preferentially wetted by (a) water and by (b) oil. Figure 4.6. Definition of the contact angle 0 for a particle adsorbed at the water-oil interface. Case where the particle is preferentially wetted by (a) water and by (b) oil.
One-Step Activation Process. In a one-step activation process, the sensitizing and nucleating solutions are combined into one solution. It is assumed that when this solution is made up, it contains various Sn-Pd chloride complexes (24). These complexes may subsequently transform into colloidal particles of metallic Pd or a metallic alloy (Sn/Pd) to form a colloidal dispersion (19,28). This dispersion is unstable. It may be stabilized by addition of an excess of Sn ions. In this case, Pd particles adsorbed on the nonconductor surface are surrounded by Sn ions. The latter must be removed by solubilizing before electroless plating so that the catalytic Pd on the surface will become exposed, freely available, to subsequent plating. An example of such a solubilizing solution is a mixture of fluoroboric and oxalic acids in a dilute solution, or just plain NaOH or HCl. [Pg.155]

In this case the quantity n indicates how many times the number of reactive particles adsorbed per unit surface increases under illumination (other external conditions remaining the same). Evidently, the rate of the heterogeneous reaction in which these particles participate will be a function of fi and thus will be sensitive to illumination. If An = Ap = 0 (photo-electrically inactive absorption of light), then according to (41) m = 1, and illumination has no effect on the reaction rate. [Pg.245]

In colloidal systems, van der Waals forces play a prominent role. When any two particles (neutral or with charges) come very close to each other, the van der Waals forces will be strongly dependent on the surrounding medium. In a vacuum, two identical particles will always exhibit an attractive force. On the other hand, if two different particles are present in a medium (in water), then there may be repulsion forces. This can be due to one particle adsorbing with the medium more strongly than with the other particle. One example will be silica particles in water medium and plastics (as in wastewater treatment). It is critical to understand under what conditions it is possible that colloidal particles remain suspended. For example, if paint aggregates in the container, then it is obviously useless for its intended purpose. [Pg.142]

The investigation of the exact ECS of small particles adsorbed on a flat (monociystalhne) substrate appears to be an excellent way to determine the relative orientation dependence of y(0) and from there the relative step and step interaction energies, provided the ECS exhibits all orientations, such that the conversion to y(0) is unique [1-4]. In that sense ECS studies are an important supplement to studies of transient morphological shapes which normally yield the product of mobility x energy. [Pg.48]

Paunov VN. Novel method for determining the three-phase contact angle of colloid particles adsorbed at air-water and oil-water interfaces. Langmuir 2003 19 7970-7976. [Pg.202]

Sehnert SS, Risby TH. 1988. Chromatographic modeling of the release of particle-adsorbed molecules into synthetic alveolar surfactant. Environ Health Perspect 78 185-195. [Pg.76]

The solution composition and the nature of particles adsorbed and reduced on the electrode, as well as e-caprolactam additive, affected the electroreduction of cadmium ions [232, 233]. [Pg.783]

In practice, container walls are usually present, and the liquid is rarely free from dust particles, adsorbed gas, absorbed gas, and foreign ions. Heterogeneous nucleation refers to the formation of nuclei on a foreign object. [Pg.35]

Hexa- and other higher brominated biphenyls are expected to be present in the particle-adsorbed state in the atmosphere. These PBBs photolyze in solution and in soil (Hill et al. 1982 Ruzo and Zabik 1975 Trotter 1977). Since PBBs present in surface soil are known to photolyze, particle-sorbed PBBs present in the atmosphere may also undergo photolysis. The importance of the photochemical reaction under sunlight illumination conditions for the degradation/transformation of PBBs in air cannot be evaluated due the lack of information. [Pg.333]

The soil particles adsorb the red pigment, which is why it is important to remove as much suspended solid matter as possible from the water before you add your indicator. Any soil particles suspended in the water will cause the indicator to turn blackish. [Pg.550]

In contrast to spatial distribution, the equilibrium energy distribution of adsorbed particles cannot be violated to any substantial degree by reaction since energy is rapidly transferred between adsorbed particles and solids. Therefore, the activated complex method may be applied to rates of surface reactions. For this we consider the activated complex (transition state) of a surface reaction as a likeness of adsorbed particle (21). But, assuming that each adsorbed particle occupies only one site, it is necessary, even in the simplest kinetic model, to consider that activated complexes are able to occupy not only one, but also several surface sites (21). For example, the usual picture of a reaction between two particles adsorbed on neighboring sites involves, in fact, the notion that the activated complex occupies both sites. When the activated complex occupies several sites, this does not create any difficulty for the theory since the surface concentration of activated complexes is an infinitesimal quantity, and so the possibility of overlapping the required sites is excluded. [Pg.185]

This scheme means that H20 can be formed as a result of an impact of a H2 molecule upon an adsorbed O atom, stage 5, or in the reaction between particles adsorbed on the adjacent sites of the surface, stage 4. [Pg.190]

In scheme (53) I denotes an intermediate particle adsorbed on site Z, At, A2, B and B2 are the molecules of gaseous reaction participants. [Pg.200]

Since this formulation includes standard values of thermodynamic functions, we shall define the standard state of a particle adsorbed on a nonuniform surface and the standard state of a free site. A uniform surface with one substance adsorbed is at its standard state at coverage 1/2 (Section IV). In order to apply this definition to each site of a nonuniform surface, we shall restate it as follows a surface site is in its standard state if the probability that it is occupied is 1/2 (in other words, if it is occupied and is vacant equally often). [Pg.209]

Garvey et al.85) made a similar sedimentation study on poly(vinyl alcohol) adsorbed on polystyrene latex particles. Adsorbance of the polymer was also measured. Both the thickness of the adsorbed layer and the adsorbance increased linearly with the square root of the molecular weight. The volume occupied by a polymer molecule in the adsorbed layer was approximately equal to that of the effective hydrodynamic sphere in bulk solution. However, the measured values of LH were greater than the hydrodynamic diameters of the polymer coils in solution. Thus, it may be concluded that adsorbed poly(vinyl alcohol) assumes a conformation elongated in the direction normal to the surface. [Pg.46]


See other pages where Adsorbents particle is mentioned: [Pg.405]    [Pg.74]    [Pg.97]    [Pg.101]    [Pg.177]    [Pg.22]    [Pg.150]    [Pg.624]    [Pg.257]    [Pg.173]    [Pg.925]    [Pg.151]    [Pg.69]    [Pg.294]    [Pg.106]    [Pg.254]    [Pg.69]    [Pg.153]    [Pg.135]    [Pg.41]    [Pg.208]    [Pg.143]   
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Adsorbed particles

Adsorbed particles

Adsorbed particles, coverage

Adsorbed redox particle

Adsorbent particles, bound

Adsorbent within particles

Adsorbents particle size distribution

Electron energy levels of adsorbed particles

Electron level of adsorbed particles

Interaction Forces (Energies) Between Particles or Droplets Containing Adsorbed Non-ionic Surfactants and Polymers

Particle density, general properties adsorbents

Particles with Adsorbed Polymer Layers

Polymeric surfactants steric stabilization, particle -adsorbed layer

Quasi-Particle Properties of Hole Levels in Solids and Adsorbate Systems

Rates of Adsorption into Adsorbent Particles

Repulsion, adsorbed particles

Silica particles polymers adsorbed

Slab adsorbent particle

Transfer Resistance of Adsorbent Particles

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