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1. |
CONDUCTANCES OF CONCENTRATED AQUEOUS SOLUTIONS OF MIXED ELECTROLYTES |
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Canadian Journal of Chemistry,
Volume 36,
Issue 10,
1958,
Page 1325-1331
A. N. Campbell,
E. M. Kartzmark,
A. G. Sherwood,
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摘要:
Equivalent conductances, viscosities, and densities were determined for solutions equimolar in two of the three salts lithium nitrate, ammonium nitrate, and silver nitrate. The three possible combinations of two salts were each studied at 25 °C and at 35 °C.The observed conductances and viscosities were compared with those of the single salt solutions at the same total ion concentration. The conductances were lower than the mean of the conductances of the single salt solutions. The viscosities were also lower than the mean viscosities.
ISSN:0008-4042
DOI:10.1139/v58-196
出版商:NRC Research Press
年代:1958
数据来源: NRC
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2. |
SOME THERMODYNAMIC CONSIDERATIONS OF THE EFFECTS OF STRESS ON METAL ELECTRODE POTENTIALS |
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Canadian Journal of Chemistry,
Volume 36,
Issue 10,
1958,
Page 1332-1337
E. A. Flood,
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摘要:
It is shown that the change in thermodynamic potential of a solid when elastically strained by the application of the principal stressespx,py, andpzis given by the equationwherevis the volume per unit mass andis the shear strain work done on unit mass of the solid, atTand (px + py + pz)constant, as the relative values ofpx,py, andpzvary, i.e., as the values of the principal stresses vary from their mean.
ISSN:0008-4042
DOI:10.1139/v58-197
出版商:NRC Research Press
年代:1958
数据来源: NRC
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3. |
MICROCALORIMETRY OF THE ADSORPTION OF WATER VAPOR ON SODIUM CHLORIDE |
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Canadian Journal of Chemistry,
Volume 36,
Issue 10,
1958,
Page 1338-1345
Henry M. Papée,
Keith J. Laidler,
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摘要:
Using a microcalorimeter of the Calvet type, measurements have been made of the heats of adsorption of water vapor on microcrystals of sodium chloride, the rate of heat production being followed as a function of time. With crystals of surface areas between 1 and 15 square meters per gram it was found that three distinct processes occurred, in the following order: (1) simple adsorption of water on the surface, (2) decrease in the surface area, and (3) penetration of water into the lattice. During the second stage no adsorption could be detected. On crystals with larger surface areas there was considerable overlapping of the three phenomena, but the general mechanisms appear to be the same.
ISSN:0008-4042
DOI:10.1139/v58-198
出版商:NRC Research Press
年代:1958
数据来源: NRC
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4. |
L'ARYLATION DES QUINONES PAR LES SELS DE DIAZONIUM : IV SUR LA RÉACTION DE CES SELS AVEC LA 2,5-DIHYDROXY-p-BENZOQUINONE ET LA SYNTHÉSE DE LA 3-HYDROXY-2,5-BISPHENYL-p-BENZOQUINONE |
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Canadian Journal of Chemistry,
Volume 36,
Issue 10,
1958,
Page 1346-1349
P. Brassard,
P. L'Écuyer,
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摘要:
not available
ISSN:0008-4042
DOI:10.1139/v58-199
出版商:NRC Research Press
年代:1958
数据来源: NRC
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5. |
LIGHT ABSORPTION STUDIES: PART XI ELECTRONIC ABSORPTION SPECTRA OF NITROBENZENES |
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Canadian Journal of Chemistry,
Volume 36,
Issue 10,
1958,
Page 1350-1361
W. F. Forbes,
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摘要:
The spectra of nitrobenzenes are discussed in terms of previously proposed hypotheses relating electronic interactions and ultraviolet absorption spectra.
ISSN:0008-4042
DOI:10.1139/v58-200
出版商:NRC Research Press
年代:1958
数据来源: NRC
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6. |
LIGHT ABSORPTION STUDIES: PART XII. ULTRAVIOLET ABSORPTION SPECTRA OF BENZALDEHYDES |
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Canadian Journal of Chemistry,
Volume 36,
Issue 10,
1958,
Page 1362-1370
J. C. Dearden,
W. F. Forbes,
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摘要:
The electronic spectra of benzaldehydes in the region 220–360 mμ are recorded and discussed in terms of previously stated hypotheses. The formyl group is shown to endow benzene derivatives with spectral properties similar to those of the acetyl group in acetophenones, except that steric interactions are slightly modified.
ISSN:0008-4042
DOI:10.1139/v58-201
出版商:NRC Research Press
年代:1958
数据来源: NRC
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7. |
LIGHT ABSORPTION STUDIES: PART XIII. THE ELECTRONIC ABSORPTION SPECTRA OF RING-SUBSTITUTED ANILINES |
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Canadian Journal of Chemistry,
Volume 36,
Issue 10,
1958,
Page 1371-1380
W. F. Forbes,
I. R. Leckie,
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摘要:
A spectral analysis of benzene derivatives in terms of steric and electronic interactions is extended to ring-substituted anilines.
ISSN:0008-4042
DOI:10.1139/v58-202
出版商:NRC Research Press
年代:1958
数据来源: NRC
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8. |
SUR LA SYNTHÈSE DE QUELQUES XANTHONES POLYSUBSTITUÈES |
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Canadian Journal of Chemistry,
Volume 36,
Issue 10,
1958,
Page 1381-1383
R. Constantin,
P. L'Écuyer,
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摘要:
La synthése de la 4,6,7-triméthoxy- et de la 1-méthyl-4,6,7-triméthoxy-9-xanthone a été réalisée en faisant agir un mélande d'anhydride acétique et d'acide sulfurique sur l'acide 6-(2′-méthoxy)- ou 6-(2′-methoxy-5′-méthylphénoxy)-vératrique. La préparation de ces deux acides a été effectuée en condensant le 6-bromovératrate de méthyle avec le guaїacolate ou l'isocréosolate de potassium en présence de cuivre. La 1-carboxy-4,6,7-triméthoxy-9-xanthone, un produit de dégradation de la cularine, a été obtenue en oxydant la 1-méthyl-4,6,7-triméthoxy-9-xanthone par l'acide chromique en solution dans l'acide éthanoique
ISSN:0008-4042
DOI:10.1139/v58-203
出版商:NRC Research Press
年代:1958
数据来源: NRC
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9. |
THE KINETICS OF MOLECULAR SIEVE ACTION. SORPTION OF NITROGEN–METHANE MIXTURES BY LINDE MOLECULAR SIEVE 4A |
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Canadian Journal of Chemistry,
Volume 36,
Issue 10,
1958,
Page 1384-1397
H. W. Habgood,
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摘要:
This system illustrates "partial molecular sieve action". Methane has a higher affinity for the sorbent and hence is preferentially sorbed at equilibrium, while nitrogen diffuses through the crystal more rapidly and thus is preferentially taken up during the early stages of sorption. Measurements were made with the pure gases and with mixtures at 0 °and −79.4 °C. The sorption isotherms fit Langmuir equations and the isosteric heats of sorption are essentially independent of concentration. The sorption rates for the pure gases may be characterized by diffusion coefficients,D, calculated in the usual manner assuming the flux of diffusion to be proportional to the concentration gradient. The resultant values forDincrease with increasing sorbate concentration. Diffusion of a mixture may be formally characterized byD's for each component. While that for methane is approximately the same as for methane alone,Dfor nitrogen in mixtures is much larger than for the pure gas and also varies with composition. This, as well as the existence of a temporary maximum in the amount of nitrogen sorbed, may be explained by considering the driving force for diffusion to be the gradient in chemical potential rather than in concentration.
ISSN:0008-4042
DOI:10.1139/v58-204
出版商:NRC Research Press
年代:1958
数据来源: NRC
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10. |
RADIATION CHEMISTRY OF SOLUTIONS: II DOSE-RATE, ENERGY, AND TEMPERATURE DEPENDENCE OF A LEUCO TRIARYLMETHANE DOSIMETER SOLUTION |
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Canadian Journal of Chemistry,
Volume 36,
Issue 10,
1958,
Page 1398-1404
W. A. Armstrong,
G. A. Grant,
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摘要:
The dose-rate, energy, and temperature dependence of the system l0−4 M4,4′-(5-chloro-2-thenylidene)bis[N,N-dimethylaniline], l0−4 Mferrous ammonium sulphate, 0.1 Msodium chloride, and 7 × 10−3 Mhydrochloric acid has been investigated. No energy dependence was observed in the range 0.16 to 2.0 Mev and no dose-rate dependence was observed in the range 4 to 230 rads/minute. However, with dose rates of 400 to 1200 rads/minute, postirradiation dye fading was observed. In the dosage range 0 to 1000 rads this fading is not extremely serious. The system is slightly temperature dependent at temperatures lower than 30 °C and markedly dependent at higher temperatures. Dye yields of samples irradiated at 30 °C were 10% higher than those of samples irradiated at 15° but 33% lower than those of samples irradiated at 45°.
ISSN:0008-4042
DOI:10.1139/v58-205
出版商:NRC Research Press
年代:1958
数据来源: NRC
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