REFRACTIVE INDEX OF He4: LIQUID

1958 ◽  
Vol 36 (7) ◽  
pp. 884-898 ◽  
Author(s):  
M. H. Edwards

Changes in the phase refractive index n with temperature have been measured between 1.6 and 4.2° K at λ = 5462.27 Å, for liquid He4 at its saturated vapor pressure, using a metal optical cryostat and a Jamin interferometer. A novel adaptation of the Jamin interferometer has been made so that, in addition, an absolute determination of the group refractive index, nG, could be made using white light of "effective wavelength" 5595 ± 40 Å. When the dispersion correction is made, the phase index for the Hg green line at T55E = 3.700° K is n = 1.026124 ± 0.000035. The relative measurements have been adjusted to this value. The more than 200 experimental points show a random scatter of less than 5 × 10−6 in index. Using Kerr's density data the polarizability is thus (N0α) = (0.12454 ± 0.00021) cm3 mole−1 at λ = 5462.27 Å, for liquid He4 at 3.7 °K. Within experimental error (N0α) is found to be independent of temperature. Thus the refractive index data may be considered as a measurement of the liquid density and coefficient of expansion.The region near the λ-point is of special interest. The expansion coefficient determined from the refractive index, βn, may be represented within experimental error by 103βnI = +41.5 + 14.5 log|T−Tλ| for T > Tλ, from about 0.1° above Tλ to within 0.01° of Tλ; and by 103βnII = −1.5 + 14.5 log |T−Tλ| for T < Tλ, from about 0.1° below Tλ to within 0.002° of Tλ. This implies that the density–temperature curve has both a vertical tangent and a point of inflection at the λ-point; and that the maximum in density occurs about 0.001° above the λ-point.

1960 ◽  
Vol 33 (4) ◽  
pp. 1132-1141
Author(s):  
Lawrence A. Wood ◽  
Irving Madorsky ◽  
Rolf A. Paulson

Abstract The procedure described attains its accuracy and precision by the refinement and improvement of conventional simple operations over a periods of years. The trend in analysis recently is, of course, toward the use of rapid physical methods. In a great many instances these involve relative measurements requiring the initial establishment of reference materials with compositions determined by methods such as the one here described, which bases the numbers derived solely on readings of an analytical balance. In fact, as already mentioned, one of the principal applications of the present method has been in the establishment of the relation between refractive index and styrene content for SBR polymers so that refractive index measurements can be used in routine determinations of bound styrene content.


2018 ◽  
Vol 58 (1) ◽  
pp. 9
Author(s):  
Filip Dvořáček

The main aim of the research was to evaluate numeric procedures of the indirect determination of the group refractive index of air and to choose the suitable ones for requirements of ordinary and high accuracy distance measurement in geodesy and length metrology. For this purpose, 10 existing computation methods were derived from various authors’ original publications and all were analysed for wide intervals of wavelengths and atmospheric parameters. The determination of the phase and the group refractive indices are essential parts in the evaluation of the first velocity corrections of laser interferometers and electronic distance meters. The validity of modern procedures was tested with respect to updated CIPM-2007 equations of the density of air. The refraction model of Leica AT401 laser tracker was analysed.


1983 ◽  
Vol 27 ◽  
Author(s):  
L. Salamanca-Riba ◽  
B.S. Elman ◽  
M.S. Dresselhaus ◽  
T. Venkatesan

ABSTRACTRutherford backscattering spectrometry (RBS) is used to characterize the stoichiometry of graphite intercalation compounds (GIC). Specific application is made to several stages of different donor and acceptor compounds and to commensurate and incommensurate intercalants. A deviation from the theoretical stoichiometry is measured for most of the compounds using this non-destructive method. Within experimental error, the RBS results agree with those obtained from analysis of the (00ℓ) x-ray diffractograms and weight uptake measurements on the same samples.


Photonics ◽  
2021 ◽  
Vol 8 (2) ◽  
pp. 41
Author(s):  
Najat Andam ◽  
Siham Refki ◽  
Hidekazu Ishitobi ◽  
Yasushi Inouye ◽  
Zouheir Sekkat

The determination of optical constants (i.e., real and imaginary parts of the complex refractive index (nc) and thickness (d)) of ultrathin films is often required in photonics. It may be done by using, for example, surface plasmon resonance (SPR) spectroscopy combined with either profilometry or atomic force microscopy (AFM). SPR yields the optical thickness (i.e., the product of nc and d) of the film, while profilometry and AFM yield its thickness, thereby allowing for the separate determination of nc and d. In this paper, we use SPR and profilometry to determine the complex refractive index of very thin (i.e., 58 nm) films of dye-doped polymers at different dye/polymer concentrations (a feature which constitutes the originality of this work), and we compare the SPR results with those obtained by using spectroscopic ellipsometry measurements performed on the same samples. To determine the optical properties of our film samples by ellipsometry, we used, for the theoretical fits to experimental data, Bruggeman’s effective medium model for the dye/polymer, assumed as a composite material, and the Lorentz model for dye absorption. We found an excellent agreement between the results obtained by SPR and ellipsometry, confirming that SPR is appropriate for measuring the optical properties of very thin coatings at a single light frequency, given that it is simpler in operation and data analysis than spectroscopic ellipsometry.


2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Pavel Malakhovsky ◽  
Dmitry Murausky ◽  
Dmitry Guzatov ◽  
Sergey Gaponenko ◽  
Mikhail Artemyev

Abstract We examined systematically how self-assembled monolayers (SAMs) of different mercaptoacids affect the spectral shift of the localized surface plasmon resonance in silver nanoplates and nanospheres. We observed a clear trend in the magnitude of a redshift with a molecular length or the SAM thickness within a homologous series of aliphatic mercaptoacids: the thicker shell the stronger the red shift. Using classic Mie theory for plasmonic core-dielectric shell spheres and oblate spheroids we developed the method for determination of a pseudo-refractive index in SAM of different molecules and obtained a good correlation with the reference refractive indices for bulk long-chain aliphatic acids, but only in case of silver nanoplates. Calculations for silver core–shell nanospheres gave overestimated values of refractive index perhaps due to restrictions of Mie theory on the minimum particle size.


2020 ◽  
Vol 8 ◽  
pp. 100065
Author(s):  
Laurent Lamaignère ◽  
Guido Toci ◽  
Barbara Patrizi ◽  
Matteo Vannini ◽  
Angela Pirri ◽  
...  

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