Chemical nature of particles

Table 13.1 shows the physical and chemical nature of particles, from molecular level to 10 mm size. Table 13.1 can be divided into three sections ... 

TABLE 13.1 The Physical and Chemical Nature of Particles, from Molecular Level to 10 mm Size... 

Chemical Nature of Particles. The chemical nature of particle surfaces is an important aspect of the coagulation rate because it determines whether two particles will join to form a new, larger particle after a collision. The tendency of two particles to stick is expressed by using an experimentally determined parameter known as the collision efficiency factor, the sticking efficiency, or the stickiness, and denoted by the symbol a. It is usually thought of as the probability that two colliding particles will stick (31). 

With increasing attention being paid to the chemical nature of particles and the effect that they may have on gas analysis, it may be necessary to remove particles from the air sample upstream of the bubbler. In fact, it may also be necessary to remove undesired gases before the bubbler if they are known to interfere with the determination of a particular analyte. 

For carbon-black fillers, structure, particle size, particle porosity, and overall physico-chemical nature of particle surface are important factors in deciding cure rate and degree of reinforcement attainable. The pH of the carbon black has a profound influence. Acidic blacks (channel blacks) tend to retard the curing process while alkaline blacks (furnace blacks) produce a rate-enhancing effect in relation to curing, and may even give rise to scorching. 

Hamaker constant Chemical nature of particles and medium... 

Fluidyibsorbamy. Fluids like ink penetrate into paper during the printing process. The further the ink penetrates, the less glossy the print. The degree of penetration in paper is generally a function of the paper porosity and wettabiUty by the fluid. It can be controlled by the particle size, shape, and chemical nature of the filler or filler surface. In particular, plate-like fillers, such as clays, tend to produce the best fluid holdout because they tend to overlap and reduce the porosity at the paper surface (see Inks). 

If an adsorbed chemical group (anchor) is more strongly bound to the surface than a solvent molecule would be at that site, an equiHbrium expression may be written for the displacement of solvent by adsorbate. Adsorption is particularly strong if the chemical nature of the adsorbed group is similar to that of the particle surface for example, in aqueous systems perfluoroalkane groups adsorb weU on polytetrafluoroethene particles and aromatic polyethene oxides adsorb weU on polystyrene. 

Plasticization, whether internal (by copolymerization) or external (with additives), is also extremely important for proper performance at the time of apphcation. The ease of coalescence and the wetting characteristics of the polymer emulsion particles are related to their softness and the chemical nature of the plasticizer. 

The stmcture of residual char particles after devolatilization depends on the nature of the coal and the pyrolysis conditions such as heating rate, peak temperature, soak time at the peak temperature, gaseous environment, and the pressure of the system (72). The oxidation rate of the chat is primarily influenced by the physical and chemical nature of the chat, the rate of diffusion and the nature of the reactant and product gases, and the temperature and pressure of the operating system. The physical and chemical characteristics that influence the rate of oxidation ate chemical stmctural variations, such as the... 

As might be expected, large differences in the removabiUty of soHd particulate soil are due to differences in the chemical nature of the particle surface. Thus, kon oxides, lampblacks, and clays, all of the same particle size, differ greatly in thek redeposition behavior and the manner in which they are removed. 

Analysis of thermal decomposition of molecules on hot surfaces of solids is of considerable interest not only for investigation of mechanisms of heterogeneous decomposition of molecules into fragments which interact actively with solid surfaces. It is of importance also for clarifying the role of the chemical nature of a solid in this process. Furthermore, pyrolysis of molecules on hot filaments made of noble metals, tungsten, tantalum, etc., is a convenient experimental method for producing active particles. Note that it allows continuous adjustment of the intensity of the molecular flux by varying the temperature of the filament [8]. 

The darkness associated with dense interstellar clouds is caused by dust particles of size =0.1 microns, which are a common ingredient in interstellar and circum-stellar space, taking up perhaps 1% of the mass of interstellar clouds with a fractional number density of 10-12. These particles both scatter and absorb external visible and ultraviolet radiation from stars, protecting molecules in dense clouds from direct photodissociation via external starlight. They are rather less protective in the infrared, and are quite transparent in the microwave.6 The chemical nature of the dust particles is not easy to ascertain compared with the chemical nature of the interstellar gas broad spectral features in the infrared have been interpreted in terms of core-mantle particles, with the cores consisting of two populations, one of silicates and one of carbonaceous, possibly graphitic material. The mantles, which appear to be restricted to dense clouds, are probably a mixture of ices such as water, carbon monoxide, and methanol.7... 

In this group of disperse systems we will focus on particles, which could be solid, liquid or gaseous, dispersed in a liquid medium. The particle size may be a few nanometres up to a few micrometres. Above this size the chemical nature of the particles rapidly becomes unimportant and the hydrodynamic interactions, particle shape and geometry dominate the flow. This is also our starting point for particles within the colloidal domain although we will see that interparticle forces are of great importance. 

Sorption of pharmaceuticals onto the surface of particulate matter or their distribution between two phases (water and either sludge, sediment or soil) depends on many factors, the most important being liquid phase pH and redox potential, the stereochemical structure and chemical nature of both the pharmaceutical compound and the sorbent, the lipophilicity of the sorbed molecules (excellent sorption at log Kov > 4, low sorption at log < 2.4), the sludge-water distribution coefficient Kd Kd > 2 L g SS good sorption, < 0.3 L g SS low sorption), the extent of neutral and ioiuc species present in the wastewater and the characteristics of the suspended particles. Moreover, the presence of humic and fulvic substances may alter the surface properties of the sludge, as well as the number of sites available for sorption and reactions, thereby enhancing or suppressing sorption of PhCs [38, 55, 61]. 

More so, inasmuch as the surface treatment can, generally speaking, lead to a displacement of the Fermi level, it follows that if the condition (27) is satisfied for a given sample, the condition (28) may be satisfied for another sample of the same material (which has undergone a different treatment). This means that particles of a given kind may act as donors or acceptors depending not only on the chemical nature of the semiconductor, but also on the biography of the adsorbent sample. 

The heat produced by the reaction of a pyrolant is dependent on various physicochemical properties, such as the chemical nature of the fuel and oxidizer, the fractions in which they are mixed, and their physical shapes and sizes. Metal particles are commonly used as fuel components of pyrolants. When a metal particle is oxidized by gaseous oxidizer fragments, an oxide layer is formed that coats the particle. If the melting point of the oxide layer is higher than that of the metal particle, the metal oxide layer prevents further supply of the oxidizer fragments to the metal, and so the oxidation remains incomplete. If, however, the melting point of the oxide layer is lower than that of the metal particle, the oxide layer is easily removed and the oxidation reaction can continue. 

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