Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Particle size external surface

Although a number of filler characteristics influence composite properties, particle size, specific surface area, and surface energetics must again be mentioned here. All three also influence interfacial interactions. In the case of large particles and weak adhesion, the separation of the matrix/ filler interface is easy, debonding takes place under the effect of a small external load. Small particles form aggregates which cause a deterioration in the mechanical properties of the composites. Specific surface area, which depends on the particle size distribution of the filler, determines the size of the contact surface between the polymer and the filler. The size of this surface plays a crucial role in interfacial interactions and the formation of the interphase. [Pg.116]

Particles consist of both internal and external surface area. The external surface area represents that caused by exterior topography, whereas the internal surface area measures that caused by microcracks, capillaries, and closed voids inside the particles. Since the chosen surface area technique should relate to the ultimate use of the data, not all techniques are useful for fine powders. The commonly used approaches are permeametry and gas adsorption according to the Brunauer, Emmet, and Teller (BET) equation [9]. Because of simplicity of operation and speed of operation, permeametry methods have received much attention. The permeametry apparatus consists of a chamber for placing the material to be measured and a device to force fluid to flow through the powder bed. The pressure drop and rate of flow across the powder bed are measured and related to an average particle size and surface area. Especially for porous powders, permeametry data include some internal surface area, thus decreasing their value. [Pg.134]

Circulating fluidized-beds do not contain any in-bed tube bundle heating surface. The furnace enclosure and internal division wall-type surfaces provide the required heat removal. This is possible because of the large quantity of soflds that are recycled internally and externally around the furnace. The bed temperature remains uniform, because the mass flow rate of the recycled soflds is many times the mass flow rate of the combustion gas. Operating temperatures for circulating beds are in the range of 816 to 871°C. Superficial gas velocities in some commercially available beds are about 6 m/s at full loads. The size of the soflds in the bed is usually smaller than 590 p.m, with the mean particle size in the 150—200 p.m range (81). [Pg.527]

The relationship between adsorption capacity and surface area under conditions of optimum pore sizes is concentration dependent. It is very important that any evaluation of adsorption capacity be performed under actual concentration conditions. The dimensions and shape of particles affect both the pressure drop through the adsorbent bed and the rate of diffusion into the particles. Pressure drop is lowest when the adsorbent particles are spherical and uniform in size. External mass transfer increases inversely with d (where, d is particle diameter), and the internal adsorption rate varies inversely with d Pressure drop varies with the Reynolds number, and is roughly proportional to the gas velocity through the bed, and inversely proportional to the particle diameter. Assuming all other parameters being constant, adsorbent beds comprised of small particles tend to provide higher adsorption efficiencies, but at the sacrifice of higher pressure drop. This means that sharper and smaller mass-transfer zones will be achieved. [Pg.291]

The additive should provide a thin layer of solids having high porosity (0.85 to 0.90) over the filter medium s external surface. Suspension particles will ideally form a layered cake over the filter aid cake layer. The high porosity of the filter aid layer will ensure a high filtration rate. Porosity is not determined by pore size alone. High porosity is still possible with small size pores. [Pg.107]

Finally, one must know the effect of catalyst particle size on Kw. For a pore diffusion-controlled reaction, activity should be inversely proportional to catalyst particle diameter, that is directly proportional to external catalyst surface area. [Pg.75]

The shape of an object is a descriptor of the outline of its external surface only. Thus the shape of an object is a property that reflects the recognized pattern of relationships among all the points that constitute its external surface. The difference between the shapes of two objects arises from the differences between the patterns of relationships among these point coordinates corresponding to the two shapes. While the size of an object, for example a material particle, is an indicator of the quantity of matter contained in it, its shape is concerned with the pattern according to which this quantity of matter is assembled together. Shape is an intrinsic rather than an extrinsic characteristic in that it is not additive. [Pg.121]

The packing itself may consist of spherical, cylindrical, or randomly shaped pellets, wire screens or gauzes, crushed particles, or a variety of other physical configurations. The particles usually are 0.25 to 1.0 cm in diameter. The structure of the catalyst pellets is such that the internal surface area far exceeds the superficial (external) surface area, so that the contact area is, in principle, independent of pellet size. To make effective use of the internal surface area, one must use a pellet size that minimizes diffusional resistance within the catalyst pellet but that also gives rise to an appropriate pressure drop across the catalyst bed. Some considerations which are important in the handling and use of catalysts for fixed bed operation in industrial situations are discussed in the Catalyst Handbook (1). [Pg.426]

In spite of such positive effects of the presence of ammonia during preparation, the particles sizes remain important on Au/FAU-2, comparable to particles previously described for similar Au/zeolites [1,2]. Noticeably, they are much bigger than expected from the insertion of the Au particles inside the pores. On the contrary, very small gold nanoparticles with a mean diameter of about 2 nm are obtained on the BEA support, that can be due to the textural properties and high external surface area of this support made... [Pg.90]

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 electronic microscopy method on the EM-125 (fig. 1) for definition of ZnCFO particles size and characteristic of its surface was applied. Known zinc oxide was chosen as the object of comparison. The electronic photos of powders testify, that new composite and zinc oxide have external similarity under the form of particles, wide range on dispersiveness (0,4-6,0 microns for zinc oxide, fig. la 0,3-6,0 microns for ZnCFO, fig. lb) also contain as crystal as amorphous phases in their structure. [Pg.191]


See other pages where Particle size external surface is mentioned: [Pg.137]    [Pg.288]    [Pg.12]    [Pg.155]    [Pg.105]    [Pg.64]    [Pg.212]    [Pg.149]    [Pg.155]    [Pg.348]    [Pg.330]    [Pg.253]    [Pg.2173]    [Pg.101]    [Pg.475]    [Pg.476]    [Pg.421]    [Pg.397]    [Pg.538]    [Pg.164]    [Pg.65]    [Pg.76]    [Pg.442]    [Pg.376]    [Pg.384]    [Pg.248]    [Pg.59]    [Pg.101]    [Pg.225]    [Pg.380]    [Pg.96]    [Pg.132]    [Pg.521]    [Pg.191]    [Pg.212]    [Pg.541]    [Pg.127]    [Pg.112]    [Pg.105]   
See also in sourсe #XX -- [ Pg.13 , Pg.14 ]




SEARCH



Particle size surface

Particle surfaces

© 2024 chempedia.info