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Standard fibre

Figure 7. Influence of the polarization preservation in a fibre interferometer. Right Standard fibre use leads to a complex pulse response associated with fringe degradations with polarization crosstalk. Left Using polarization preserving fibre, the two polarization modes give rise to contrasted fringes and can be separated using a polarizer. Figure 7. Influence of the polarization preservation in a fibre interferometer. Right Standard fibre use leads to a complex pulse response associated with fringe degradations with polarization crosstalk. Left Using polarization preserving fibre, the two polarization modes give rise to contrasted fringes and can be separated using a polarizer.
Lorentz corrections. As can be seen, there are significant changes in the resolved parameters, particularly the peak positions and peak heights the effect on peak width is less marked. The standard fibre correction (LOR 1) gives the most reasonable results, the correction (LOR 2), suggested for the equatorial trace of a fibre specimen, is not considered to be realistic. [Pg.156]

Determination of the fibre type, including checking of the stated fibre type, is one of the most important preliminary tests. If no IR spectrometer is available, standard fibres can be most readily identified using the characteristic reactions according to Stratmann. For modified fibres or high-performance and speciality fibres the more complicated classification on the basis of solubility groups and their subdivisions or other methods of analysis have to be used. [Pg.152]

Qualitative analysis of standard fibres by means of microscopy and characteristic reactions can be carried out as follows ... [Pg.152]

Approximate values in °C (d = decomposition). Standard fibres emphasized. [Pg.167]

It is as if the displacements of the central point of the octahedron were relocated to every ligand site. The elementary function space of the displacements of the central atom, which transforms as the translational irrep, Tu, is called the standard fibre. This fibre is attached to every site of the cluster, and the set of these fibres is the fibre bundle. The action of the group permutes fibres of the bundle. The following induction theorem holds ... [Pg.149]

Theorem 14 Consider a standard fibre, consisting of a function space that is invariant under the action of the group. In a cluster of equivalent sites, we can form a fibre bundle by associating this standard fibre with every site position. The induced representation of the fibre bundle is then the direct product of the irrep of the standard fibre with the positional representation. [Pg.149]

All the SiC fibres are circular in cross-section with diameters of 15 p,m or less. The earliest SiC fibres, the Nicalon 100 series, showed all the fracture characteristics of a glassy structure, although TEM studies showed the presence of very small SiC grains of less than 2 nm as well as even smaller free carbon particles. The Nicalon 200 series became the standard fibre used for most ceramic matrix composites. The fibre has a diameter of 15 p.m and also shows a glassy fracture morphology, as Fig. 2 reveals. [Pg.78]

The analysis of the radial intensity distribution along the azimuthal angle j in the q region around 12 nm of Fig. 11.8a-c reveals that during the development of the fibrillar morphology, for deformations lower than the critical value at which transformation of y form into mesophase is complete, there is a portion of the crystalline lamellae which tend to orient with the chain axes nearly perpendicular to the stretching direction instead than parallel, contrary to what expected in the standard fibre morphology. [Pg.308]

As the author pointed out in the first edition of this book, the likelihood of discovering new important general purpose materials was remote but special purpose materials could be expected to continue to be introduced. To date this prediction has proved correct and the 1960s saw the introduction of the polysulphones, the PPO-type materials, aromatic polyesters and polyamides, the ionomers and so on. In the 1970s the new plastics were even more specialised in their uses. On the other hand in the related fields of rubbers and fibres important new materials appeared, such as the aramid fibres and the various thermoplastic rubbers. Indeed the division between rubbers and plastics became more difficult to draw, with rubbery materials being handled on standard thermoplastics-processing equipment. [Pg.9]

In addition to standard grades varying in the ABS/PC ratio, fire-retarded, glass-fibre-reinforced and glass-fibre-reinforced fire-retarded grades are available. Typical properties of three grades of ABS-PC alloys are given in Table 20.9. [Pg.579]

The classification as a carcinogen need not apply to fibres with a length weighted geometric mean diameter less two standard errors greater than 6 pm Sodium dichromate Sodium dichromate dihydrate... [Pg.95]

The first step in the analysis of this situation is the transformation of the applied stresses on to the fibre axis. Referring to Fig. 3.10 it may be seen that Ox and Oy may be resolved into the x, y axes as follows (the reader may wish to refer to any standard Strength of Materials text such as Benham, Crawford and Armstrong for more details of this stress transformation) ... [Pg.184]

As stated in Section I, columns should be selected so the low molar mass portions of the samples in question can be sufficiently separated from the elution interval of the system peaks. This task cannot always be accomplished, e.g., dimethylacetamide often replaces dimethylformamide as a GPC eluent the analyzed, mostly polar, samples require a neutral salt (e.g., FiBr) (7). The calibration is usually carried out with poly(methylmethacrylate) standards... [Pg.439]

PP/Uvasil 299 fibres were analysed by 1II NMR after dissolution (toluene)/precipitation (methanol) and PP/Uvasil 299 pellets after reflux extraction with precipitation (methanol) of the oligomers [619]. The dried extracts were redissolved in CDCI3, containing the DMP internal standard. The method allows quantification of the high-MW HALS at very low levels (0.044 0.001 %). [Pg.150]

Identification of dyes on dyed textiles is traditionally carried out by destructive techniques [493], TLC is an outstanding technique for identification of extracted dyestuffs and examination of inks. Figure 4.9 shows HPTLC/SERRS analysis of acridine orange [492], Wright et al. [494] have described a simple and rapid TLC-videodensitometric method for in situ quantification of lower halogenated subsidiary colours (LHSC) in multiple dye samples. The results obtained by this method were compared with those obtained by an indirect TLC-spectrophotometric method and those from HPLC. The total time for the TLC-videodensitometric assay of five standards and four samples applied to each plate was less than 45 min. The method is applicable for use in routine batch-certification analysis. Loger et al. [495,496] have chromatographed 19 basic dyes for PAN fibres on alumina on thin-layer with ethanol-water (5 2) and another 11 dyes on silica gel G with pyridine-water... [Pg.229]


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See also in sourсe #XX -- [ Pg.149 ]




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