Review of optical scintillation methods of measuring the refractive-index spectrum, inner scale and surface fluxes

1992 ◽  
Vol 2 (3) ◽  
pp. 179-201 ◽  
Author(s):  
Reginald J Hill
1996 ◽  
Vol 50 (8) ◽  
pp. 1047-1057 ◽  
Author(s):  
John E. Bertie ◽  
Zhida Lan

The previously reported nonreproducibility of the intensity of the OH stretching band of liquid water has been explored. It was found that it can be eliminated in measurements with the Circle® multiple ATR cell by ensuring that the ATR rod is coaxial with the glass liquid holder. It was also found that normal laboratory temperature variations of a few degrees change the intensity by ⩽∼1% of the peak height. A new imaginary refractive index spectrum of water has been determined between 4000 and 700 cm1 as the average of spectra calculated from ATR spectra recorded by four workers in our laboratory over the past seven years. It was obtained under experimental and computational conditions superior to those used previously, but is only marginally different from the spectra reported in 1989. In particular, the integrated intensities of the fundamentals are not changed significantly from those reported in 1989. The available imaginary refractive index, k, values between 15,000 and 1 cm−1 have been compared. The values that are judged to be the most reliable have been combined into a recommended k spectrum of H2O(l) at 25 °C between 15,000 and 1 cm−1, from which the real refractive index spectrum has been calculated by Kramers–Kronig transformation. The recommended values of the real and imaginary refractive indices and molar absorption coefficients of liquid water at 25 ± 1 °C are presented in graphs and tables. The real and imaginary dielectric constants and the real and imaginary molar polarizabilities in this wavenumber range can be calculated from the tables. Conservatively estimated probable errors of the recommended k values are given. The precision with which the values can be measured in one laboratory and the relative errors between regions are, of course, far smaller than these probable errors. The recommended k values should be of considerable value as interim standard intensities of liquid water, which will facilitate the transfer of intensities between laboratories.


2018 ◽  
Vol 879 ◽  
pp. 227-233
Author(s):  
Weeratouch Pongruengkiat ◽  
Thitika Jungpanich ◽  
Kodchakorn Ittipornnuson ◽  
Suejit Pechprasarn ◽  
Naphat Albutt

Refractive index and Abbe number are major physical properties of optical materials including glasses and transparent polymers. Refractive index is, in fact, not a constant number and is varied as a function of optical wavelength. The full refractive index spectrum can be obtained using a spectrometer. However, for optical component designers, three refractive indices at the wavelengths of 486.1 nm, 589.3 nm and 656.3 nm are usually sufficient for most of the design tasks, since the rest of the spectrum can be predicted by mathematical models and interpolation. In this paper, we propose a simple optical instrumental setup that determines the refractive indices at three wavelengths and the Abbe number of solid and liquid materials.


1998 ◽  
Vol 37 (22) ◽  
pp. 5169 ◽  
Author(s):  
Mitsunori Saito ◽  
Norihisa Matsumoto ◽  
Jiro Nishimura

2021 ◽  
pp. 000370282110367
Author(s):  
Thomas G. Mayerhöfer ◽  
Vladimir Ivanovski ◽  
Jürgen Popp

We suggest a new modality of infrared spectroscopy termed Infrared Refraction Spectroscopy, which is complimentary to absorption spectroscopy. The beauty of this new modality lies not only in its simplicity but also in the fact that it closes an important gap: It allows to quantitatively interpret reflectance spectra by simplest means. First, the refractive index spectrum is calculated from reflectance by neglecting absorption. The change of the refractive index is proportional to concentration, and the spectra with features similar to second derivative absorbance spectra can simply be computed by numerically deriving the refractive index spectra, something which can be easily carried out by standard spectra software packages. The peak values of the derived spectra indicate oscillator positions and are approximately proportional to the concentration in a similar way as absorbance is. In contrast to absorbance spectra, there are no baseline ambiguities for first derivative refractive index spectra, and in refractive index spectra, instead of integrating over a band area, a simple difference of two refractive index values before and after an absorption leads to a quantity that correlates perfectly linearly with concentration in the absence of local field effects.


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