INDEX difference between

In general, the multiphasic heterogenous nature of the impact grade styrene-based polymers is the root cause of their opaque-turbid nature. In determining the transparency of the blends, size and the size-distribution pattern of the dispersed phase along with the refractive index difference between the continuous and the dispersed phases are two very important criterion [133]. 

In this study, four Styragel columns were utilized one column had a nominal porosity rating of 10, two colvtmns of 10, and the fourth column of 10 A. The refractometer was maintained at 37°C. A 5 ml syphon was used to monitor a solvent flow rate of 1 ml/min. The instrviment was run at the highest sensitivity setting because the refractive index difference between our solvent and polymer was only moderate and because a number of samples analyzed had a broad molecular weight distribution (MWD). 

Figure 1. Schematic of the optical fiber system. Excitation light is launched into the fiber. Due to the refractive index differences between the fiber core and cladding materials, the light is internally reflected and travels through the fiber with minimal loss (see inset). The emitted light is carried back from the fluorescent sensor located on the tip of the fiber to a CCD camera detector. Reprinted with permission from Science, 2000, 287, 451-452. Copyright 2000 AAAS.

The ideal HPLC detector should have the same characteristics as those required for GC detectors, i.e. rapid and reproducible response to solutes, a wide range of linear response, high sensitivity and stability of operation. No truly universal HPLC detector has yet been developed but the two most widely applicable types are those based on the absorption of UV or visible radiation by the solute species and those which monitor refractive index differences between solutes dissolved in the mobile phase and the pure mobile phase. Other detectors which are more selective in their response rely on such solute properties as fluorescence, electrical conductivity, diffusion currents (amperometric) and radioactivity. The characteristics of the various types of detector are summarized in Table 4.14. 

In general, measuring beads requires less laser power than measuring cells because of their higher index of refraction (n 1.5 for polystyrene beads vs. n 1.37 for cells).15 The optical force imparted to a particle scales with the difference in index of refraction between the particle and the fluidic medium.16 For bead measurements, we typically operate at a laser power of 2.5 W, whereas for cell measurements the laser is operated at 10 W to obtain similar displacements. These relative power levels are in line with the comparative refractive index differences between the two different particle types and water. 

Those experimentalists who use spectrophotometry or spectrofluorimetry to measure rates of biochemical reactions should always be mindful that bubble clearance frequently displays first-order kinetics. This applies to bubbles adhering to the inside wall of the cuvette as well as bubbles released from solution itself. The presence of bubbles within a cuvette may introduce artifactual kinetic behavior resulting (a) from refractive index differences between the gas trapped in the bubbles and that of the test solution, and (b) from the high reflectance of the air/water interface surrounding some bubbles. 

There are small changes in serum albumin concentration with age, with concomitant small effects on protein binding of some highly bound drugs such as naproxen, salicylate, and warfarin. For such drugs the free concentration rather than the total plasma concentration is a better predictor of drug dose requirements, particularly for drugs with low therapeutic index (difference between the therapeutic... 

Where n is the refractive index difference between the polymer in... 

In dark-field, as in direct observation microscopy, the refractive index difference between... 

Coleman et al. 2471 reported the spectra of different proportions of poly(vinylidene fluoride) PVDF and atactic poly(methyl methacrylate) PMMA. At a level of 75/25 PVDF/PMMA the blend is incompatible and the spectra of the blend can be synthesized by addition of the spectra of the pure components in the appropriate amounts. On the other hand, a blend composition of 39 61 had an infrared spectrum which could not be approximated by absorbance addition of the two pure spectra. A carbonyl band at 1718cm-1 was observed and indicates a distinct interaction involving the carbonyl groups. The spectra of the PVDF shows that a conformational change has been induced in the compatible blend but only a fraction of the PVDF is involved in the conformational change. Allara M9 250 251) cautioned that some of these spectroscopic effects in polymer blends may arise from dispersion effects in the difference spectra rather than chemical effects. Refractive index differences between the pure component and the blend can alter the band shapes and lead to frequency shifts to lower frequencies and in general the frequency shifts are to lower frequencies. 

Here h is the thickness of the ultracentrifuge centerpiece (usually 12 mm), n — n0 is the refractive index difference between the solution (n) and the solvent (n0), and A is the wavelength of light used (generally 546 /a). Thus with the Rayleigh optical system one can obtain n, which can be expressed as... 

Liquid chromatographs are equipped with a means to continuously monitor the column effluent and recognize the presence of solute. Only small sample sizes are used with most HPLC columns, so a detector must have high sensitivity. The type of detector that has the most universal application is the differential refiractometer. This device continuously monitors the refractive index difference between the mobile phase (pure solvent) and the mobile phase containing sample (column effluent). The sensitivity of this detector is on the order of 0.1 ju,g, which, compared to other detectors, is only moderately sensitive. The major advantage of the refractometer detector is its versatility its main limitation is that there must be at least 10 7 refractive index units between the mobile phase and sample. 

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