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Type size structures

We have considered briefly the important macroscopic description of a solid adsorbent, namely, its speciflc surface area, its possible fractal nature, and if porous, its pore size distribution. In addition, it is important to know as much as possible about the microscopic structure of the surface, and contemporary surface spectroscopic and diffraction techniques, discussed in Chapter VIII, provide a good deal of such information (see also Refs. 55 and 56 for short general reviews, and the monograph by Somoijai [57]). Scanning tunneling microscopy (STM) and atomic force microscopy (AFT) are now widely used to obtain the structure of surfaces and of adsorbed layers on a molecular scale (see Chapter VIII, Section XVIII-2B, and Ref. 58). On a less informative and more statistical basis are site energy distributions (Section XVII-14) there is also the somewhat laige-scale type of structure due to surface imperfections and dislocations (Section VII-4D and Fig. XVIII-14). [Pg.581]

The discussion of diffraction so far has made no reference to the size of the 2D grating. It has been assumed that the grating is infinite. In analogy with optical or X-ray diffraction, finite sizes of the ordered regions on the surface (finite-sized gratings) broaden the diffracted beams. From an analysis of the diffracted-beam shapes, the types of structural disorder in the surface region can be identified and quantified. - ... [Pg.257]

Bonded repair sizes, shapes and configurations vary greatly depending on the type of structure and size and location of damage. Typically the damaged area is removed and replacement details of like material and size are prepared to fit. Larger doublers and possibly triplers are installed over the replacement details to hold them in place and transfer load to them. Fig. 23 shows a typical bonded repair for a small damaged area on honeycomb bonded structure. [Pg.1170]

Surface preparation is of prime importance, and optimum performance of modern protection coatings can be achieved only if the surface of the steel has been adequately treated. The method of surface preparation depends on the shape and size of the structure or component. Thus it is preferable to blast-clean an openwork steel structure by manual methods, since with this type of structure automatic blast cleaning would lead to excessive impingement of the abrasive on the machine itself. [Pg.45]

The telluride halides crystallize in monoclinic lattices, but only In-TeBr and InTel are isotypic 162). InTeCl forms a layer type of structure, as do InSCl and its analogs, but, owing to the size of the Te atom and the enhanced covalency of the In-Te bond, only a coordination number of 4 for indium is realized. The structure is built up of strongly distorted, InTesraCli/j tetrahedra that share the corners and edges occupied by Te atoms. The Cl atoms are coordinated to one tetrahedron each, and do not take part in the layer formation 324, 325). [Pg.388]

N2 adsorption-desorption isotherms revealed that MCs had hi surface area (>1200 m /g) and large pore volume (>1.0 cm /g). From SAXS patterns of the prepared materials, it was confirmed that pores of SBA-15 and CMK-3 retained highly ordered 2-dimensional hexagonal type arrangement [5], while MCM-48 had 3-dimensional cubic type pore structure. It should be noted that a new scattering peak of (110) appeared in the CMK-1 after the removal of MCM-48 template. Furthermore, the pore size of CMK-1 and the wall thickness of MCM-48 were found to be 2.4 nm and 1.3 nm, respectively. This result demonstrates that a systematic transformation of pore structure occurred during the replication process from MCM-48 to CMK-1 [6]. [Pg.610]

PHA synthases are the key enzymes of PHA biosynthesis. These enzymes catalyze the covalent linkage between the hydroxyl group of one and the carboxyl group of another hydroxyalkanoic acid. The substrates of PHA synthases are the coenzyme A thioesters of hydroxyalkanoic acids there is no evidence that PHA synthases can utilize either free hydroxyalkanoic acids or other derivatives of hydroxyalkanoic acids. With respect to size, structure, and substrate specificity, three different types of PHA synthases (I, II, and III) can be distinguished (see below). [Pg.85]

While antibodies display similar structures - in fact, various types of IgGs are commonly used in immunoassays, antigens and proteins show tremendous variations in size, structure and charge strongly effecting the array performance. [Pg.491]

Figure 9.3 shows the relationship between ionic radius and proton affinity in a graphical way for monatomic ions having a — 1 charge. It is clear that to a good approximation there is a correlation between the size of the anion and its proton affinity. While this is in no way a detailed study, it is clear that the smaller (and thus harder] the negative ion (with the same type of structure) the more strongly it binds a proton. [Pg.304]

In case of [M(edt)2] based salts, the size of the small anion is similar to the size of the CsMes ligand of the cation and only type I structural motives (D+ A D+ A-chains) were observed. For the intermediate size anionic complexes, [M(tdx)2], [M(mnt)2] and [Ni(a-tpdt)2], the most common structural motive obtained in salts based on those anions is also of type I. For the larger anionic complexes, [M(bdx)2] and [M(dmix)2], types III and IV chain arrangements were observed. In both cases anion molecules (type IV) or face-to-face pair of anions (type III) alternate with side-by-side pairs of cations. The complexes [M(mnt)2] and [M(dmix)2] (M = Ni, Pd and Pt) frequently present dimerization in the solid state [19], and they are the only anions where the chain arrangements present face-to-face pairs of anions (structural motives II and III). The variety of structural... [Pg.103]

Increasing the size of PAHs makes their deposition on surfaces difficult because they can neither be sublimed nor made sufficiently soluble for solution processing. A precursor route has thus been designed according to which molecules are deposited on a surface and transformed into the final disc-type adsorbate structures in a thermal solid-state reaction with the substrate surface acting as a template.1261 An exciting example is the hexaether 41 (scheme 11) which is sublimed onto a Cu-(1U) sur-... [Pg.326]

In order to facilitate satisfactory dye uptake, the molecular size of a disperse dye must be kept small monoazo structures are therefore exceptionally important, particularly in the coloration of polyester and cellulose triacetate. In the yellow shade area, molecular size generally poses no problem and the various available coupling components can all be used without making the molecule too large. A very simple example of the type of structure employed using a phenolic coupling component is Cl Disperse Yellow 3 (4-72). This dye is known to cause skin sensitisation when on nylon [85] and can also provoke an allergic reaction [86]. [Pg.212]

The first kind of simplification exclusively concerns the size of the basis set used in the linear combination of one center orbitals. Variational principle is still fulfilled by this type of "ab initio SCF calculation, but the number of functions applied is not as large as necessary to come close to the H. F. limit of the total energy. Most calculations of medium-sized structures consisting for example of some hydrogens and a few second row atoms, are characterized by this deficiency. Although these calculations belong to the class of "ab initio" investigations of molecular structure, basis set effects were shown to be important 54> and unfortunately the number of artificial results due to a limited basis is not too small. [Pg.16]

CHA (-34, -44, -47), ERI (-17), GIS (-43), LEV (-35), LTA (-42), FAU (-37) and SOD (-20). Also shown is the pore size and saturation water pore volume for each structure type. The structures include the first very large pore molecular sieve, VPl-5, with an 18-ring one-dimensional channel with a free pore opening of 1.25 nm [29], large pore (0.7-0.8nm), intermediate pore (0.6nm), small pore (0.4 nm) and very small pore (0.3 nm) materials. Saturation water pore volumes vary from 0.16 to 0.35cm /g, comparable to the pore volume range observed in zeolites (see Chapter 2 for detailed structures). [Pg.9]

Tropocollagen molecules are firmly linked together, particularly at their ends, by covalent networks of altered lysine side chains. The number of these links increases with age. Type IV collagens form networks with a defined mesh size. The size-selective filtering effect of the basal membranes in the renal glomeruli is based on this type of structure (see p. 322). [Pg.344]

These motivations strengthen the interest for eatalysis towards the development of ordered assemblies of ID nanostruetures for oxide materials, e.g. metal-oxide catalysts in which the 3D macro-structure is constituted by an ordered assembling of regular ID structures with nanometric size. Note that this type of structure is significantly different from that of metal-oxide supported over other metal-oxides, such as monolayer-type V202/Ti02 materials. See also later, when the concept of nanostructured metal-oxide films is defined. [Pg.84]

Several studies have considered the influence of filler type, size, concentration and geometry on shear yielding in highly loaded polymer melts. For example, the dynamic viscosity of polyethylene containing glass spheres, barium sulfate and calcium carbonate of various particle sizes was reported by Kambe and Takano [46]. Viscosity at very low frequencies was found to be sensitive to the network structure formed by the particles, and increased with filler concentration and decreasing particle size. However, the effects observed were dependent on the nature of the filler and its interaction with the polymer melt. [Pg.171]

Carbon black Finely divided carbon made by incomplete combustion or decomposition of natural gas or petroleum-based oils in different types of equipment. According to the process and raw material used, it can be furnace (e.g., HAF), thermal (e.g., MT), or channel carbon black (e.g., EPC), each having different characteristics, such as particle size, structure, and morphology. The addition of different types of carbon blacks to rubber compounds results in different processing behavior and vulcanizate properties. [Pg.251]


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See also in sourсe #XX -- [ Pg.378 ]




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Sized Structures

Type size

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