Elements of Chromotherapy, the Administration of Ultra-violet, Infra-red, and Luminous Rays through Color FiltersElements of Chromotherapy, the Administration of Ultra-violet, Infra-red, and Luminous Rays through Color Filters. By HowatR. Douglas, L.R.C.P. (Edin.), L.R.C.S. (Edin.), L.R.F.P.S. (Glas.), with a Foreword by GauvainHenrySir, M.D., M.Chir., F.R.C.S. A volume of 106 pages, with 20 illustrations. Published by The Actinic Press, Ltd., London, 1938. Price: 8∕6d.

Radiology ◽  
1938 ◽  
Vol 30 (4) ◽  
pp. 519-519
Keyword(s):  
2015 ◽  
Vol 9 (1) ◽  
pp. 2303-2310
Author(s):  
Abderrahim Benchaib ◽  
Abdesselam Mdaa ◽  
Izeddine Zorkani ◽  
Anouar Jorio

The vanadium dioxide VO₂ currently became very motivating for the nanotechnologies’ researchers. It makes party of the intelligent materials because these optical properties abruptly change semiconductor state with metal at a critical  temperature θ = 68°C. This transition from reversible phase is carried out from a monoclinical structure characterizing its semiconductor state at low temperature towards the metal state of this material which becomes tétragonal rutile for  θ ˃ 68°C ; it is done during a few nanoseconds. Several studies were made on this material in a massive state and a thin layer. We will simulate by Maple the constant optics of a thin layer of VO₂ thickness z = 82 nm for the metal state according to the energy ω of the incidental photons in the energy interval: 0.001242 ≤ ω(ev) ≤ 6, from the infra-red (I.R) to the ultra-violet (U.V) so as to be able to control the various technological nano applications, like the detectors I.R or the U.V,  the intelligent windows to  increase  the energy efficiency in the buildings in order to save the cost of energy consumption by electric air-conditioning and the paintings containing nano crystals of this material. The constant optics, which we will simulate, is: the index of refraction, the reflectivity, the transmittivity, the coefficient of extinction, the dielectric functions ԑ₁ real part and  ԑ₂  imaginary part of the permittivity complexes ԑ of this material and the coefficient absorption. 


2015 ◽  
Vol 8 (2) ◽  
pp. 2148-2155 ◽  
Author(s):  
Abderrahim Benchaib ◽  
Abdesselam Mdaa ◽  
Izeddine Zorkani ◽  
Anouar Jorio

The vanadium dioxide is a material thermo chromium which sees its optical properties changing at the time of the transition from the phase of semiconductor state ↔ metal, at a critical temperature of 68°C. The study of the optical properties of a thin layer of VO₂ thickness 82 nm, such as the dielectric function, the index of refraction, the coefficient ofextinction, the absorption’s coefficient, the reflectivity, the transmittivity, in the photonic spectrum of energy ω located inthe interval: 0.001242 ≤ ω (ev) ≤ 6, enables us to control well its practical utility in various applications, like the intelligentpanes, the photovoltaic, paintings for increasing energy efficiency in buildings, detectors of infra-red (I.R) or ultra-violet(U.V). We will make simulations with Maple and compare our results with those of the literature


Polymers ◽  
2021 ◽  
Vol 13 (5) ◽  
pp. 829
Author(s):  
Galina M. Mamardashvili ◽  
Dmitriy A. Lazovskiy ◽  
Ilya A. Khodov ◽  
Artem E. Efimov ◽  
Nugzar Z. Mamardashvili

New coordination oligomers and polymers of Sn(IV)-tetra(4-sulfonatophenyl)porphyrin have been constructed by the chelation reaction of its diaxialphenolates with Cu2+. The structure and properties of the synthesized polyporphyrin arrays were investigated by 1H Nuclear Magnetic Resonance (1H NMR), Infra Red (IR), Ultra Violet - Visible (UV-Vis) and fluorescence spectroscopy, mass spectrometry, Powder X-Rays Diffraction (PXRD), Electron Paramagnetic Resonance (EPR), thermal gravimetric, elemental analysis, and quantum chemical calculations. The results show that the diaxial coordination of bidentate organic ligands (L-tyrazine and diaminohydroquinone) leads to the quenching of the tetrapyrrole chromophore fluorescence, while the chelation of the porphyrinate diaxial complexes with Cu2+ is accompanied by an increase in the fluorescence in the organo-inorganic hybrid polymers formed. The obtained results are of particular interest to those involved in creating new ‘chemo-responsive’ (i.e., selectively interacting with other chemical species as receptors, sensors, or photocatalysts) materials, the optoelectronic properties of which can be controlled by varying the number and connection type of monomeric fragments in the polyporphyrin arrays.


Hydrogen ◽  
2021 ◽  
Vol 2 (2) ◽  
pp. 160-206
Author(s):  
Ernest Ilisca

Hydrogen molecules exist in the form of two distinct isomers that can be interconverted by physical catalysis. These ortho and para forms have different thermodynamical properties. Over the last century, the catalysts developed to convert hydrogen from one form to another, in laboratories and industries, were magnetic and the interpretations relied on magnetic dipolar interactions. The variety concentration of a sample and the conversion rates induced by a catalytic action were mostly measured by thermal methods related to the diffusion of the o-p reaction heat. At the turning of the new century, the nature of the studied catalysts and the type of measures and motivations completely changed. Catalysts investigated now are non-magnetic and new spectroscopic measurements have been developed. After a fast survey of the past studies, the review details the spectroscopic methods, emphasizing their originalities, performances and refinements: how Infra-Red measurements characterize the catalytic sites and follow the conversion in real-time, Ultra-Violet irradiations explore the electronic nature of the reaction and hyper-frequencies driving the nuclear spins. The new catalysts, metallic or insulating, are detailed to display the operating electronic structure. New electromagnetic mechanisms, involving energy and momenta transfers, are discovered providing a classification frame for the newly observed reactions.


1883 ◽  
Vol 36 (228-231) ◽  
pp. 137-138

M. Fievez has recently sent me a map of the solar spectrum from C to A* inclusive, and as part of this region is one which I have been measuring, I have examined the new publication with great interest. Photography and eye measurements do not exactly coincide in the detail of the grouping of the little a group as far as A, and A itself is shown by M. Fievez’s map as wanting some details which appear in the photographs. Thus in the photographs there are some seventeen lines, whilst in M. Fievez’s map there are but thirteen. Between A and a there are several lines of marked intensity in the photograph which are not shown in the new map. The wave-lengths of the different lines from above “ a ” to A are not the same as those given by Fievez, when they are taken from comparison photo-graphs of the 1st order of the red and 2nd of the ultra-violet on the same plate, or when checked by photographs of the 2nd order of the red with the 3rd order of the green taken in a similar manner. In my paper, “Phil. Trans.,” Part II, 1880, I gave a method of using mirrors by which this could be effected, but since Professor Rowland introduced his concave gratings this is much more readily carried out. He has kindly furnished me with gratings for the purpose, having about 14,400 lines to the inch, with focal distances of 7 feet 6 inches and 12 feet 6 inches respectively. These have been employed in determining the wave-lengths of this part of the spectrum. Cornu’s map was used as a reference for the ultra-violet wave-lengths, and Ångström’s map for those in the blue and green. The two maps may be taken as equally exact. The determination of A has been made by Maseart, Smyth, and others, besides Ångström and Langley, with discordant results. I think the above may be taken as accurate as are Cornu’s and Ångström maps.


Since March, 1909--in connection with the Glass Workers' Cataract Committee of the Royal Society--I have been experimenting on the effect of adding various metallic oxides to the constituents of glass in order to cut off the invisible rays at the ultra-violet and the infra-red ends of the spectrum. The work has been done chiefly in my own laboratory. I have been aided by Mr. Harry Powell, of the Whitefriars Glass Works, who prepared several pots of coloured glass from my formulae on a much larger scale than could be made outside a glass works. From these glasses cylinders and sheets were made. The main object of this research is to prepare a glass which will cut off those rays from highly heated molten glass, which damage the eyes of workmen, without obscuring too much light or materially affecting the colours of objects seen through the glass when fashioned into spectacles, but the work necessitated an examination of the screening properties of glass plates for ultra-violet and luminous light, and therefore the research was enlarged so as to embrace the three forms of radiation.


1991 ◽  
Vol 20 (11) ◽  
pp. 8-10
Author(s):  
David Pelling

The optical rotation of quartz has been measured over a large band of wavelengths. We have Gumlich’s original work over the range from λ = 2·140 μ to λ = 0·21935 μ , repeated and extended into the ultra-violet by Soret and Sarasin and Guye. More recently a series of accurate measurements covering the same range was published by Lowry, and then Duclaux and Jeantet gave a series of results for a range in the ultra-violet from λ = 0·30876 μ to λ = 0·1853980 μ . Finally, Lowry and Coode-Adams, having improved the accuracy of their original method, succeeded in obtaining a very accurate set of readings extending from λ = 2·5170 μ in the infra-red to λ = 0·2280 μ in the ultra-violet, reaching thus just up to the region measured by Duclaux and Jeantet. Various attempts have been made to fit these results into a formula. Gumlich found it possible to represent his results by a formula of the type ω = α 1 /λ 2 + α 2 /λ 4 + α 3 /λ 6 + α 4 /λ 8 + α 5 /λ 10 , but Kettler had almost equal success with the simpler form ω = (λ 2 α)/β.


2003 ◽  
Vol 25 (2) ◽  
pp. 201 ◽  
Author(s):  
C Marks ◽  
F Busana ◽  
F Gigliotti ◽  
M Lindeman

MAMMALS do not normally visually perceive infrared (IR) or ultra-violet (UV) light that exists on either side of the visual spectrum from 390 to 760 nanometers (nm) (Wolken 1975). There is no evidence to suggest that nocturnal mammals have become more sensitive to long wavelength light as an adaptive response (Lythgoe 1979), although some reptiles can sense longer wavelength, thermal IR radiation (Barrett et al. 1970). Because it is not perceived, and is unlikely to affect animal behaviour, IR observation can be an invaluable tool for wildlife researchers. This paper describes the construction and use of simple IR radiation sources that can be used for non-invasive behavioural observations of captive and free-ranging mammals.


The spectra of many diatomic free radicals like those of CH, OH, NH, C 2 , CN have been known and identified as such almost since the beginning of molecular spectroscopy. They occur readily in emission in a variety of flames (including the ordinary Bunsen burner) and in electric discharges. It was through the study of these spectra that our knowledge of the structure of diatomic molecules was developed and in particular that the different coupling conditions between the electron spin and the other angular momenta were recognized. Most of the resonance transitions of the diatomic free radicals lie in the visible or near ultra-violet region where a detailed high-resolution study is easily possible. It is for this reason also that these spectra play a most prominent part in the spectra of astrophysical sources: comets, low-temperature stars and the interstellar medium. The spectra of free polyatomic radicals have become recognized and analyzed only in the last ten or fifteen years. The reason for this delay is the much greater complexity of the spectra of polyatomic as compared to the spectra of diatomic molecules combined with the greater difficulty of exciting these spectra in emission. Ordinary polyatomic molecules can easily be studied in infra-red absorption or by means of the Raman effect. The infra-red and Raman spectra are simpler than the electronic spectra and their interpretation has been established for a long time; but up to now no infra-red (or Raman) spectrum of a free polyatomic radical has been obtained. One is entirely dependent on electronic spectra for the study of the structure of polyatomic free radicals, and these electronic spectra exhibit many complexities.


Sign in / Sign up

Export Citation Format

Share Document