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M-band

Fig. 3. Attenuation of infrared as a function of normalized concentration caused by CO absorption in the 4.6 p.m band. = 6.6E3 ppm m,... Fig. 3. Attenuation of infrared as a function of normalized concentration caused by CO absorption in the 4.6 p.m band. = 6.6E3 ppm m,...
There are two main kinds of dye aggregates, characterized by their typical spectral properties J-aggregates and H-aggregates. The absorption band maximum (f-band) of the J-aggregates is shifted bathochromicaHy with respect to that of an isolated molecule (M-band) the absorption maximum of the H-aggregates is shifted hypsochromicaHy (H-band). The dyes can also form dimers with a shorter absorption wavelength (D-band). [Pg.494]

FIGURE 17.21 A drawing of the arrangement of the elastic protein titin in the skeletal mnscle sarcomere. Titin filaments originate at the periphery of the M band and extend along the myosin filaments to the Z lines. These titin filaments produce the passive tension existing in myofibrils that have been stretched so that the thick and thin filaments no longer overlap and cannot interact. (Adapted from Ohtsuki, ., Maruyama, K, and Ebashi,. S ., 1986. Advances ia Protein Chemisti y 38 1—67.)... [Pg.550]

Band, m. volume binding.—n. band ribbon, tape, strap, strip, belt, hoop hinge bond, tie, ligament, -achst, m. banded agate, ribbon agate. [Pg.56]

Band-feder, /. flat spring, -fdrderer, m. belt conveyor, -kante, /. edge of a band, band head, -mass, n. tape measure, -stabl, m. band steel, strip steel, bandstreifig, a. banded, streaked, striped. Band-trockuer, m. belt drier, -wunn, m. tapeworm. [Pg.56]

Bund, m. band, tie hoop, collar, flange alliance. — n. bundle, bunch. [Pg.85]

Streifen, m. band, strip, stripe, stria streak, vein (in marble, etc.) strap, -gefiige, n. banded structure, -kohle, /. banded coal, -spektrum, n. band spectrum. [Pg.432]

The challenges of achieving high QE over the 0.3-1.1 m band is summarized in Eig. 14, which shows the optical absorption depth of photons in silicon with the range of thickness of different regions of a CCD. Figure 14, which we like to call the beautiful plot captures the information needed for understanding the QE of silicon CCDs. [Pg.142]

This is the usual situation in a high field. It is characterized by the fact that transitions between different M bands of the spectrum are highly improbable because of the vanishingly small relevant density of states or because of the high number of spins that have to be rearranged in order to distribute a Zeeman quantum over... [Pg.302]

M. Band and T. Treasure, Ion-Selective Electrodes in Medicine and Medical Research, in Ion-Selective Electrode Methodology (ed. A. K. Covington),... [Pg.133]

Henner, D.J. Yang, M Band, L. Shimotsu, H. Ruppen, M. Ferrari, E. Proc. 5th Inti. Symp. on Genetics of Industrial Microorganisms 1986, p81. [Pg.94]

Petrek M, Otyepka M, Bands P et al (2006) CAVER a new tool to explore routes from protein clefts, pockets and cavities. BMC Bioinformatics 7 316-325... [Pg.162]

Figure 1 shows that photoirradiation of the samples pretreated at 350°, 450°, 550° C causes an increase in intensity of the 540-600-nm H+M-M+ band. This indicates the formation of additional M+ cation radicals under these conditions. The slight increase in intensity of the 540-600-nm band for the sample treated at 550° C, compared with the samples treated at 350° and 450° C, is apparently limited by the number of proton-donating sites and MH+ ions associated with it. The absence of H+M-M+ after M+ cation radicals are formed (sample treated at 750° C) can be caused by the complete absence of proton-donating sites and consequently by the impossibility of forming MH+ ions. Special attention should be paid to the effects caused by photoirradiation of the samples heat treated at 200° and 650°C. The appearance of H+M-M+ in the first case can be explained by assuming that the photoirradiation itself produces some M+ cation radicals from excess of MH+ ions. In the second case excess M+ cation radicals are observed on photoirradiation. The 540-600-nm band was observed after treatment at 650° C in type Y zeolites only (see Table I). [Pg.248]

Kurbatov and Neuimin attributed the 1.39-m band to adsorbed CHC13. They account for its decreasing intensity by postulating that the band is unique for the adsorbed state and disappears when liquid CHC13 is formed... [Pg.34]

C. Further A-Band Analysis C-Protein, Titin, and the Vertebrate M-Band. 61... [Pg.17]


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See also in sourсe #XX -- [ Pg.27 , Pg.64 ]




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Filament Structure and the M-Band

M-C bands

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