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Characteristics, structural

Azo dyes make up the major proportion of the direct dyes apart from these, only a few azine, phthalocyanine, and nonazo metal-complex dyes possess a certain significance. The following structural characteristics are necessary for high substantivity  [Pg.159]

The experimental procedures for determining particle size and shape [Pg.6]

Observation of the movement of particles in response to an applied force (see Chapter 2). [Pg.6]

Direct observation of particle images (microscopy and electron microscopy) (see Chapter 3). [Pg.6]

Measurements which relate to the total surface area of the particles (gas adsorption and adsorption from solution) (see Chapters 5 and 6). [Pg.6]

While isolating human PS-PLAi cDNA we found a similar cDNA, designated PS-PLAiAC, with four extra bases (GTAC) inserted at the boundary of the exon-intron junction (nt 1122) [23]. The insertion of these four bases caused a frame shift, resulting in the loss of about 80 amino acid residues at the C-terminus (Fig. 2.1). The mRNA having this sequence was found in various human tissues and cell lines [23]. Although it is not clear whether the short form of the enzyme is actually expressed at the protein level, experiments using the recombinant proteins prepared with the baculovirus system revealed the functional difference of the two isoforms (see below) [23]. [Pg.29]


Settlement and. structural characteristics of landfills. The settlement of landfills depends on the initial compaction, characteristics of wastes, degree of decomposition, and effects of consolidation when the leachate and gases are formed in the landfill. The height of the completed fill will also influence the initial compaction and degree of consolidation. [Pg.2257]

Dynamic structural characteristics can also be interpreted in terms of resonance. There is a substantial barrier to rotation about the C—N single bonds in carboxamides. A frequently observed consequence is the nonidentity of NMR peaks due to the syn and anti... [Pg.10]

In order for a substitution to occur, a n-complex must be formed. The term a-complex is used to describe an intermediate in which the carbon at the site of substitution is bonded to both the electrophile and the hydrogen that is displaced. As the term implies, a a bond is formed at the site of substitution. The intermediate is a cyclohexadienyl cation. Its fundamental structural characteristics can be described in simple MO terms. The a-complex is a four-7t-electron delocalized system that is electronically equivalent to a pentadienyl cation (Fig. 10.1). There is no longer cyclic conjugation. The LUMO has nodes at C-2 and C-4 of the pentadienyl structure, and these positions correspond to the positions meta to the site of substitution on the aromatic ring. As a result, the positive chargex)f the cation is located at the positions ortho and para to the site of substitution. [Pg.553]

In this section the rosins and rosin derivative resins, coumarone-indene and hydrocarbon resins, polyterpene resins and phenolic resins will be considered. The manufacture and structural characteristics of natural and synthetic resins will be first considered. In a second part of this section, the characterization and main properties of the resins will be described. Finally, the tackifier function of resins in rubbers will be considered. [Pg.597]

Most researchers were not apparently aware of earlier CNT preparations in the context of ultra-thin vapour-grown carbon fibres (VGCF). This type of CNT is termed pyrolytic (PCNT) and its preparation shows promise of large-scale synthesis. Needless to say, it is of practical importance to provide sufficient CNTs at reasonable cost. This chapter highlights the preparation methods, structural characteristics and current commercial status of PCNTs and includes a description of the devices used hitherto to obtain aligned PCNTs. By way of... [Pg.143]

An alternative form of the right-handed double helix is A-DNA. A-DNA molecules differ in a number of ways from B-DNA. The pitch, or distance required to complete one helical turn, is different. In B-DNA, it is 3.4 nm, whereas in A-DNA it is 2.46 nm. One turn in A-DNA requires 11 bp to complete. Depending on local sequence, 10 to 10.6 bp define one helical turn in B-form DNA. In A-DNA, the base pairs are no longer nearly perpendicular to the helix axis but instead are tilted 19° with respect to this axis. Successive base pairs occur every 0.23 nm along the axis, as opposed to 0.332 nm in B-DNA. The B-form of DNA is thus longer and thinner than the short, squat A-form, which has its base pairs displaced around, rather than centered on, the helix axis. Figure 12.13 shows the relevant structural characteristics of the A- and B-forms of DNA. (Z-DNA, another form of DNA to be discussed shortly, is also depicted in Figure 12.13.) A comparison of the structural properties of A-, B-, and Z-DNA is summarized in Table 12.1. [Pg.367]

The majority of analgesics can be classified as either central or peripheral on the basis of their mode of action. Structural characteristics usually follow the same divisions the former show some relation to the opioids while the latter can be recognized as NSAlD s. The triamino pyridine 17 is an analgesic which does not seem to belong stmcturally to either class. Reaction of substituted pyridine 13 (obtainable from 12 by nitration ) with benzylamine 14 leads to the product from replacement of the methoxyl group (15). The reaction probably proceeds by the addition elimination sequence characteristic of heterocyclic nucleophilic displacements. Reduction of the nitro group with Raney nickel gives triamine 16. Acylation of the product with ethyl chlorofor-mate produces flupirtine (17) [4]. [Pg.102]

Structural characteristics of compounds with X Me = 8 are collected in Table 17. Na3NbF8 and Na3TaF8 compounds that form similar crystal structure [77], The structure of Na3TaF8 was determined by Hoard et al. [136], by means of X-ray diffraction of a single crystal. Na3TaF8 is composed of sodium cations and isolated complex ions TaF83, in an Archimedean antiprism configuration, as shown in Fig. 23. [Pg.60]

Most of the M3MeOF6 type compounds belong to the highest symmetry class, except for Na3NbOF6. The main structural characteristics of the M3MeOF6 type compounds are collected in Table 20. [Pg.65]

Among the different families of tantalum and niobium complex fluorides and oxyfluorides, the family of compounds with an X Me ratio equal to 6 is the largest. Table 22 presents the main structural characteristics of hexafluoroniobates and hexafluorotantalates. All known cases of niobium- and tantalum-containing formulary analogs have the same crystal structure type, at least at ambient temperature. [Pg.70]

Dioxytetrafluoroniobates (-tantalates) of alkali metals for the general M3Me02F4 type also belong to the family characterized by X Me=6. Structural characteristics of the compounds are collected in Table 26. [Pg.78]

Table 28 presents structural characteristics of compounds with X Me ratios between 6 and 5 (5.67, 5.5, 5.33, 5.25). According to data provided by Kaidalova et al. [197], MsNbsC Fu type compounds contain one molecule of water to form M5Nb303Fi4-H20, where M = K, Rb, Cs, NH4. Cell parameters for both anhydrous compounds [115] and crystal-hydrates [197] were, nevertheless, found to be identical. Table 28 includes only anhydrous compound compositions because IR absorption spectra of the above compounds display no bands that refer to vibrations of the water molecule... [Pg.82]

Table 28. Structural characteristics of compounds with X Me ratios between 6 and 5. Table 28. Structural characteristics of compounds with X Me ratios between 6 and 5.
Table 32. Structural characteristics of M Ta OsFf, compounds (M = NH4, K, Rb) and Cs7TasOnF2i, with 4 < X Me<5 (all compounds have orthorhombic syngony). Table 32. Structural characteristics of M Ta OsFf, compounds (M = NH4, K, Rb) and Cs7TasOnF2i, with 4 < X Me<5 (all compounds have orthorhombic syngony).
Table 36 presents structural characteristics of oxyfluoride compounds with X Me < 3. [Pg.104]

Table 38. Structural characteristics of MeX2 type compounds. Table 38. Structural characteristics of MeX2 type compounds.
Sodium reduction development directions, 336 diluted melts, 331-332 of K-Salt, 327-328 principals, 326 Solid-phase interaction mechanism, 34-37 niobium oxyfluorides, 26-31 tantalum oxyfluorides, 32-34 Solubility diagrams (NH4)5Nb3OF18, 22 K2NbF7 in HF solutions, 14 K2TaF7 in HF solutions, 14 RbsNbjOF,, 22-23 Solubility of peroxides, 307 Specific conductivity, 153, 164 Spontaneous polarization, 223 Structural characteristics for X Me=8, 61,... [Pg.388]

In Section 4.5, we discuss the optical properties of clusters formed by sexi-thienyl molecules adopting the herringbone structure characteristic of their crystal structure [34]. The theoretical results arc compared to corresponding experimental measurements. [Pg.372]

The availability of high-intensity, tunable X-rays produced by synchrotron radiation has resulted in the development of new techniques to study both bulk and surface materials properties. XAS methods have been applied both in situ and ex situ to determine electronic and structural characteristics of electrodes and electrode materials [58, 59], XAS combined with electron-yield techniques can be used to distinguish between surface and bulk properties, In the latter procedure X-rays are used to produce high energy Auger electrons [60] which, because of their limited escape depth ( 150-200 A), can provide information regarding near surface composition. [Pg.227]

Kuznetsov GK, Irgen LA (1976) In Thermodynamic and structural characteristics of polymer interphases, Naukova Dumka, Kiev, p 94... [Pg.60]

The basics observed in molded products are always the same only the extent of the features varies depending on the process variables, material properties, and cavity contour. That is the inherent hydrodynamic skin-core structure characteristic of all IM products. However, the ratio of skin thickness to core thickness will vary basically with process conditions and material characteristics, flow rate, and melt-mold temperature difference. These inherent features have given rise to an increase in novel commercial products and applications via coinjection, gas-assisted, low pressure, fusible-core, in-mold decorating, etc. [Pg.468]


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