1000 resultados para Fournier, Joseph Anthelme (1854-1928) -- Procès -- France -- Paris (France)
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"Notice biographique sur le cheykh êl-Mohdy": t. 2, p. [7]-122.
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Mode of access: Internet.
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Goldsmiths'-Kress no. 31737.2.
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"Notice sur la vie et les ouvrages de ... Lagrange par M. Delambre"; t. 1, introduction pages 9-51.
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With: France et Rhin / par P.J. Proudhon. Paris : Librairie Internationale : A. Lacroix, Verboeckhoven & Cie, 1868.
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Mode of access: Internet.
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I. Chemistry of the aliphatic series newly tr. and rev. from the German ed. (after Prof. Edgar F. Smiths's 3d American ed.) by Percy E. Spielman. 1916. ...II. Chemistry of the carbocyclic compounds, tr. from the 11th German ed., by E.E. Fournier d'Albe. 1922. ...III. Heterocyclic compounds, Tr. from the 11th German ed., by E.E. Fournier d'Albe. 1923.
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Mode of access: Internet.
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Jean Baptiste Joseph, barão de Fourier, publicou em Paris no ano de 1822 a sua ópera magna “Théorie Analytique de la Chaleur”. Nesta obra Fourier demonstrava que a condução do calor nos corpos sólidos podia ser descrita através de uma série infinita de senos e co‐senos. O trabalho estimulou investigações nos mais variados campos da ciência e da técnica, tendo ressaltado que o tipo de formulação matemática empregada por Fourier era um pré‐requisito para a solução de fenómenos que exibiam natureza periódica. O método de exprimir funções periódicas em termos de somas de senos e co‐senos recebe o nome de Análise Harmónica. O princípio de Fourier é basicamente o seguinte: sendo dado um sinal (função) periódico representá‐lo como série de senos e co‐senos. Obviamente que se o sinal já for um seno ou co‐seno nada mais haverá para dizer (eventualmente, um termo médio não‐nulo); mas o nosso intuito é o de extrair informação de onde a haja, i.e., de funções não‐sinusoidais. Aos vários termos da série de Fourier, cada um deles de argumento múltiplo inteiro do período da função original, dá‐se‐lhes o nome de harmónicos, sendo a ordem destes precisamente o valor desse múltiplo.
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Référence bibliographique : Rol, 57341
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Référence bibliographique : Rol, 60189
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La version intégrale de ce mémoire est disponible uniquement pour consultation individuelle à la Bibliothèque de musique de l’Université de Montréal (http://www.bib.umontreal.ca/MU).
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The structures of two substituted acetylene compounds have been characterized from their microwave rotational spectra. In the first study, two structures of 6-methyl-3-heptyne have been determined. This compound can be thought of as an ethyl group separated from an isobutyl group by a C≡C spacer. Both structures have the ethyl and isobutyl groups eclipsed, consistent with the dominant interaction determining the orientation about the acetylene axis being the weak dispersion attraction between the end groups. One structure is with the isobutyl group in a symmetric conformation and the other with the isobutyl group asymmetric. In addition, the microwave spectrum of the butane analogue 3,5-octadiyne has been observed. This compound consists of two ethyl groups separated by two C≡C spacers. The study is still in progress, but it appears that the ethyl end groups are freely rotating. Therefore, it seems that the dispersion attractions between the end groups are too weak at this longer distance of about 7 Å. The structures of several fluorocarbons have also been studied by microwave spectroscopy. The structures of perfluoropentane and perfluorohexane have been shown to be helical, like the polymer polytetrafluoroethylene (Teflon©). The structure of perfluoropropane and two conformers of 1H-heptafluoropropane have been determined to be non-helical. It is apparent that the steric and dipole repulsions between fluorine atoms that have been attributed to the helical structure of longer fluorocarbon chains are not sufficient in a three carbon chain to cause a twist in the structures.
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Resumen: Descripción: calle de Constantinopla con personajes en camello y vendedores