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Surface of particles

The contact angles of water and adhesive resin on wood are higher in the case of freshly harvested wood compared to stored chips. This means that the surface of particles from this fresh wood is more hydrophobic. This influences the wetting and the penetration negatively and with this the gluability. Reason for this lower wettability of freshly harvested wood is a higher content of some wood chemical components, or wood extractives, as has been determined by water extraction. This result, however, must not be confused with the better wettability of a freshly cut surface, independently if it is freshly harvested or stored wood. [Pg.1084]

Reactions of the general type A + B -> AB may proceed by a nucleation and diffusion-controlled growth process. Welch [111] discusses one possible mechanism whereby A is accepted as solid solution into crystalline B and reacts to precipitate AB product preferentially in the vicinity of the interface with A, since the concentration is expected to be greatest here. There may be an initial induction period during solid solution formation prior to the onset of product phase precipitation. Nuclei of AB are subsequently produced at surfaces of particles of B and growth may occur with or without maintained nucleation. [Pg.71]

This equation has been used for estimating migration velocities of radionuclides (e.g. 66). Here Pr is the density of the rock (kg/m3), p the density of water, e the fissure porosity, af the specific surface of fissures in the bedrock (m2/m3) and ap the specific surface of particles used in the Kd determinations (m2/m3). The distribution coefficient Kd represents ar. equilibrium value for the particular rock under the pertinent conditions. [Pg.291]

Mass transfer from a fluid to the surface of particles... [Pg.651]

Phosphate is also ubiquitous as a minor component within the crystal lattices of other minerals or adsorbed onto the surface of particles such as clays, calcium carbonate, or ferric oxyhydroxides (Ruttenberg, 1992). Therefore, in general, transport of these other particulate phases represents an important transport pathway of P as well. [Pg.363]

A large fraction of the hazardous waste generated in industry is in the form of dilute aqueous solutions. The special challenges of separation in highly dilute solutions may be met by the development of new, possibly liquid-filled, membranes by processes involving selective concentration of toxic chemicals on the surfaces of particles or by the use of reversed micelles. [Pg.136]

Now, we show the relation between the ratio of 8 to Tq, 8/ro and the volume fraction of carbon black (p in Table 18.1, when the diameter of the hard particle (including carbon black, the GH layer and a little more contribution from the cross-links at the surface of particle) is tq and the distance between the hard particles is 8. In the carbon black-filled rubber (ip g 0.23-0.25), the fact that the stress of the filled system is 10-15 times larger than that of the unfilled rubber as shown in Figure 18.1 indicates that more than 90% of the stress of the system is supported by the supernetwork and the remainder of the stress results from the matrix rubber. In the present calculation, however, we can ignore the contribution from the matrix mbber. [Pg.533]

The sacrificial core approach entails depositing a coating on the surface of particles by either the controlled surface precipitation of inorganic molecular precursors from solution or by direct surface reactions [2,3,5,6,8,9,33-35,38], followed by removal of the core by thermal or chemical means. Using this approach, micron-size hollow capsules of yttrium compounds [2], silica spheres [38], and monodisperse hollow silica nanoparticles [3,35] have been generated. [Pg.515]

Th is extremely insoluble and adheres to the surface of particles in the ocean soon after it forms from the decay of Because these particles continuously settle from the water column, °Th is rapidly removed from the oceans to the seafloor. The combined process of surface adsorption, followed by particle settling, is termed scavenging. Measurement of the very low °Th concentrations in seawater that result from this... [Pg.499]

Snow line The distance from the Sun at which water is stable on the surface of particles leading to comets. The presence of a large planetary mass such as Jupiter can then direct comets onto Earth, providing a source of cometary molecules to a prebiotic Earth... [Pg.190]

Vp/Ap =(volume of particle)/(external surface of particle) = R/3 for spheres... [Pg.752]

In the capillaries of variable cross section or the lattice of the interconnected sites and bonds of the various size the situation is essentially different. At the beginning, the mercury is at the external surface of particles of a sample, and only the pores that are directly contiguous to external surface can be filled according to the considered model of a bunch of capillaries. The cavities with windows of size rw (F>HgX which are adequate to an equilibrium condition but inside the bulk of a sample, can be filled only under a condition of their connection to an external surface through a circuit of cavities with windows of size V > rwP already filled with mercury. Therefore, the condition for the filling of a cavity with a window of the size rm can be expressed as the requirement of a direct contact of a considered cavity with mercuiy. Accordingly, under each pressure PHg, all windows of size rWl are only poten-... [Pg.321]

The surfaces of colloidal particles are often charged and these changes can arise from a number of sources. Chemically bound ionogenic species may be found on the surface of particles such as rubber or paint latex particles. Charged species may be physically adsorbed if ionic surface active materials, for example, have been added. A charged surface may occur on a crystal lattice. An example is the isomorphous substitution of lower valency cations such as aluminium for silicon in the lattice structure of clays. A further example is the adsorption of lattice ions... [Pg.52]

The mean hydrodynamic boundary layer generated on the surface of particles undergoing a dissolution process... [Pg.148]

Richardson and Mijkle 63 1 have shown that, at high concentrations, the results of sedimentation and fluidisation experiments can be represented in a manner similar to that used by Carman" 4 1 for fixed beds, discussed in Chapter 4. Using the interstitial velocity and a linear dimension given by the reciprocal of the surface of particles per unit volume of fluid, the Reynolds number is defined as ... [Pg.277]

Ri suspension Drag force per unit surface of particle N/m2 ML- T-2... [Pg.289]

Brunauer-Emmett-Teller (BET) adsorption describes multi-layer Langmuir adsorption. Multi-layer adsorption occurs in physical or van der Waals bonding of gases or vapors to solid phases. The BET model, originally used to describe this adsorption, has been applied to the description of adsorption from solid solutions. The adsorption of molecules to the surface of particles forms a new surface layer to which additional molecules can adsorb. If it is assumed that the energy of adsorption on all successive layers is equal, the BET adsorption model [36] is expressed as Eq. (6) ... [Pg.174]

Theoretical work on inhomogeneous molecular distributions is as yet incomplete, but McNulty et al 6) have made some calculations on adsorbed molecules on the surface of particles. Their conclusion was that the angular distributions have structure and that the inelastic scattering intensity in the forward and backward directions is particularly sensitive to particle size. [Pg.371]

This has been whimsically described as the Great Particle Conspiracy. An important set of these processes involves the incorporation of trace metals into biogenic hard and soft parts. Another involves the adsorption of metals onto the surfaces of particles. Although some metals can theoretically be removed by abiotic precipitation into mineral phases, continuing research confirms that most of the trace metal removal is biologically mediated. [Pg.270]


See other pages where Surface of particles is mentioned: [Pg.271]    [Pg.295]    [Pg.1579]    [Pg.178]    [Pg.179]    [Pg.630]    [Pg.227]    [Pg.27]    [Pg.883]    [Pg.506]    [Pg.507]    [Pg.335]    [Pg.315]    [Pg.249]    [Pg.48]    [Pg.491]    [Pg.339]    [Pg.448]    [Pg.254]    [Pg.617]    [Pg.210]    [Pg.735]    [Pg.12]    [Pg.447]    [Pg.271]    [Pg.23]    [Pg.33]    [Pg.16]    [Pg.251]    [Pg.370]   
See also in sourсe #XX -- [ Pg.14 ]




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Adhesion of Cylindrical Particles to Rough Surfaces

Atomic Imaging of particle surfaces

Calculation of Metal Surface Area, Dispersion, and Particle Diameter

Deposition of Colloid Particles at Heterogeneous Surfaces

Deposition of Particles on Surfaces

Diffusion Boundary Layer Near the Surface of a Particle

Effects of Surface Roughness on Interactions with Particles

Effects on Polymer Conformation due to the Presence of Particle Surfaces and Interparticle Spacing

Energy Loss in the Interaction of Atomic Particles with Solid Surfaces

Experimental Methods for Measurement of Particle-Surface Adhesion

Flotation of Solid Particles to Liquid Surface

Mass transfer from a fluid to the surface of particles

Nonlinear, Band-structure, and Surface Effects in the Interaction of Charged Particles with Solids

Particle Flotation Technology (of Solid Particles to Liquid Surface)

Particle surfaces

Potential Energy of Interaction Between Particles and Surfaces

Preparation and Deposition of Particles on Surface

Prevention of particle deposition on bubble surface at angles

Reactions of Gases at Particle Surfaces

Shape factors of single particles specific surface

Sols of Silica Particles with Modified Surfaces

Specific surface area of particle

Spectroscopy as a Probe of Surface Electrochemistry at Metal Catalyst Particles

Surface Charge of Colloidal Particles

Surface Chemistry of Particles

Surface Cleaning of Particles

Surface Modification of Silica Particle

Surface and bulk diffusion of active particles

Surface area of particles

Surface modification of inorganic particles

Surface modification of particles

Surface modification of polymer particles

Surfaces of Nanosized Semiconductor Particles

Synthesis with Supported Metal Particles by Use of Surface Organometallic Chemistry Characterization and some Applications in Catalysis

The Capture of Particles Due to Surface and Hydrodynamic Forces

The Particle Surface as a Carrier of Functional Groups

Wetting of Pigment Particle Surfaces

Zeta Potential of Soil Particle Surfaces

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