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Determination by refractive

Why are sugar and alcohol content in foods commonly determined by refractive index determinations ... [Pg.71]

Carless, J.E., Swarbrick, J. (1964) The solubility of benzaldehyde in water as determined by refractive index measurements. J. Pharm. Pharmacol. 16, 633-634. [Pg.428]

Another important finding was made by Miers (1904), who determined, by refractive index measurements, the solution concentrations near the faces of... [Pg.225]

In syrups, the solids content (Brix, or refracto-metric dry solids (RDS)) is determined by refractive index measurement. Tables correlating refractive index with sucrose and invert content are published in the International Commission for Uniform Methods of Sugar Analysis and AO AC methods books. [Pg.4730]

Cloud point temperature (CP, determined at 1 K min- ) and coexistence ( determined by refractive index of the low and high polymer concentration phases after 24 h equilibration) curves obtained for a binary mixture of a comb-shaped poly[oligo(2-ethyl-2-oxazoline) methacrylate] in water.The coexistence curve is fitted to guide the eye (Weber et al., 2013). (Source-. Reprinted with permission from Wiley.)... [Pg.20]

The values for the D sodium line of the atomic and structural constants and of the bond refractions, as determined by the author, are collected in Tables XI,2A and XI,2B respectively. [Pg.1034]

Separations based upon differences in the physical properties of the components. When procedures (1) or (2) are unsatisfactory for the separation of a mixture of organic compounds, purely physical methods may be employed. Thus a mixture of volatile liquids may be fractionally distilled (compare Sections 11,15 and 11,17) the degree of separation may be determined by the range of boiling points and/or the refractive indices and densities of the different fractions that are collected. A mixture of non-volatile sohds may frequently be separated by making use of the differences in solubilities in inert solvents the separation is usually controlled by m.p. determinations. Sometimes one of the components of the mixture is volatile and can be separated by sublimation (see Section 11,45). [Pg.1092]

Specifications and Analytical Methods. The commercial aqueous solution is specified as 34% minimum butynediol, as determined by bromination or refractive index. Propargyl alcohol is limited to 0.2% and formaldehyde to 0.7%. [Pg.106]

Solution Polymers. Acryflc solution polymers are usually characterized by their composition, solids content, viscosity, molecular weight, glass-transition temperature, and solvent. The compositions of acryflc polymers are most readily determined by physicochemical methods such as spectroscopy, pyrolytic gas—liquid chromatography, and refractive index measurements (97,158). The solids content of acryflc polymers is determined by dilution followed by solvent evaporation to constant weight. Viscosities are most conveniently determined with a Brookfield viscometer, molecular weight by intrinsic viscosity (158), and glass-transition temperature by calorimetry. [Pg.171]

Glass-transition temperatures are commonly determined by differential scanning calorimetry or dynamic mechanical analysis. Many reported values have been measured by dilatometric methods however, methods based on the torsional pendulum, strain gauge, and refractivity also give results which are ia good agreement. Vicat temperature and britde poiat yield only approximate transition temperature values but are useful because of the simplicity of measurement. The reported T values for a large number of polymers may be found ia References 5, 6, 12, and 13. [Pg.260]

The concentration of a pure sugar solution is determined by measurements of polarization (optical rotation), refractive index, and density. [Pg.9]

It should be noted that low-loss spectra are basically connected to optical properties of materials. This is because for small scattering angles the energy-differential cross-section dfj/dF, in other words the intensity of the EEL spectrum measured, is directly proportional to Im -l/ (E,q) [2.171]. Here e = ei + iez is the complex dielectric function, E the energy loss, and q the momentum vector. Owing to the comparison to optics (jqj = 0) the above quoted proportionality is fulfilled if the spectrum has been recorded with a reasonably small collection aperture. When Im -l/ is gathered its real part can be determined, by the Kramers-Kronig transformation, and subsequently such optical quantities as refraction index, absorption coefficient, and reflectivity. [Pg.59]

Determination of the optical constants and the thickness is affected by the problem of calculating three results from two ellipsometric values. This problem can be solved by use of the oscillator fit in a suitable wavenumber range or by using the fact that ranges free from absorption always occur in the infrared. In these circumstances the thickness and the refractive index outside the resonances can be determined - by the algorithm of Reinberg [4.317], for example. With this result only two data have to be calculated. [Pg.274]

Sodium dodecyl sulfate present in hydrophilic ointments has been determined by TLC on silica gel with flame ionization detection, which was considered better than the colorimetric method. TLC is preferred to HPLC in this case due to the low sensitivity of the refractive index detector that makes difficult the analysis of small amounts of sodium dodecyl sulfate [284]. [Pg.283]

The free oil can be determined by an ion exchange HPLC technique. A solution of the sample in ethyl alcohol is analysed by high-performance ion exchange chromatography using a specially prepared ion exchange resin stationary phase, ethanol mobile phase, and differential refractive index detection. [Pg.440]

Spherical rollers were machined from AISI 52100 steel, hardened to a Rockwell hardness of Rc 60 and manually polished with diamond paste to RMS surface roughness of 5 nm. Two glass disks with a different thickness of the silica spacer layer are used. For thin film colorimetric interferometry, a spacer layer about 190 nm thick is employed whereas FECO interferometry requires a thicker spacer layer, approximately 500 nm. In both cases, the layer was deposited by the reactive electron beam evaporation process and it covers the entire underside of the glass disk with the exception of a narrow radial strip. The refractive index of the spacer layer was determined by reflection spectroscopy and its value for a wavelength of 550 nm is 1.47. [Pg.12]


See other pages where Determination by refractive is mentioned: [Pg.444]    [Pg.1244]    [Pg.524]    [Pg.309]    [Pg.55]    [Pg.261]    [Pg.444]    [Pg.1244]    [Pg.524]    [Pg.309]    [Pg.55]    [Pg.261]    [Pg.203]    [Pg.1032]    [Pg.101]    [Pg.176]    [Pg.368]    [Pg.370]    [Pg.371]    [Pg.311]    [Pg.133]    [Pg.270]    [Pg.372]    [Pg.24]    [Pg.487]    [Pg.60]    [Pg.302]    [Pg.61]    [Pg.747]    [Pg.302]    [Pg.141]    [Pg.104]    [Pg.260]    [Pg.486]    [Pg.375]    [Pg.445]    [Pg.185]    [Pg.304]    [Pg.4]   


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