1. |
THE RATE OF DEHYDRATION OF COPPER SULPHATE PENTAHYDRATE AT LOW PRESSURES OF WATER VAPOR |
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Canadian Journal of Chemistry,
Volume 31,
Issue 2,
1953,
Page 107-119
G. B. Frost,
R. A. Campbell,
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摘要:
The rate of dehydration of copper sulphate pentahydrate has been determined over a range of low pressures of water vapor. It has been found that as the pressures are increased, the rate at first drops very rapidly; this drop is followed by a period of marked acceleration, which is followed in turn by a gradual decline. Copper sulphate pentahydrate has been found to be similar in this respect to manganous oxalate dihydrate, which has been hitherto regarded as unique in its behavior. The observed effects are probably due to amorphous to crystalline transitions occurring during induction periods, the durations of which have also been found to depend on water vapor pressure.
ISSN:0008-4042
DOI:10.1139/v53-015
出版商:NRC Research Press
年代:1953
数据来源: NRC
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2. |
THE FISSION YIELD OF I131IN THE THERMAL NEUTRON FISSION OF U235 |
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Canadian Journal of Chemistry,
Volume 31,
Issue 2,
1953,
Page 120-125
Rosalie M. Bartholomew,
F. Brown,
R. C. Hawkings,
W. F. Merritt,
L. Yaffe,
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摘要:
The fission yield of I131has been investigated using improved extraction techniques and disintegration rate measurements. The value obtained for the fission yield is (3.1 ± 0.1)%. This is relative to a Ba140reference fission yield of 6.1%. The half-life for I131has been determined and found to be 8.05 ± 0.01 days.
ISSN:0008-4042
DOI:10.1139/v53-016
出版商:NRC Research Press
年代:1953
数据来源: NRC
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3. |
THE BIOGENESIS OF ALKALOIDS: VII. THE FORMATION OF HORDENINE AND N-METHYLTYRAMINE FROM TYROSINE IN BARLEY |
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Canadian Journal of Chemistry,
Volume 31,
Issue 2,
1953,
Page 126-128
Edward Leete,
Léo Marion,
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摘要:
Feedingdl-tyrosine-2-C14to sprouting barley resulted in the formation of radioactive hordenine and N-methyltyramine in the roots. Isolation and degradation of these alkaloids showed that all the activity was located in the α-carbon atom of the side chain, thus indicating that tyrosine is a precursor of N-methyltyramine and hordenine.
ISSN:0008-4042
DOI:10.1139/v53-017
出版商:NRC Research Press
年代:1953
数据来源: NRC
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4. |
THE REACTION OF ACTIVE NITROGEN WITH ACETYLENE |
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Canadian Journal of Chemistry,
Volume 31,
Issue 2,
1953,
Page 129-133
J. Versteeg,
C. A. Winkler,
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摘要:
The main products of this reaction were hydrogen cyanide and polymer that contained approximately 32% nitrogen. Yields of these substances increased to constant values with increase of acetylene flow rate. Some cyanogen and methane were also formed. The yield of cyanogen passed through a maximum with increased flow rate of acetylene, but the methane yields were quite erratic.
ISSN:0008-4042
DOI:10.1139/v53-018
出版商:NRC Research Press
年代:1953
数据来源: NRC
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5. |
ISOLATION OF THE ALDOBIURONIC ACID, 3-(XYLOPYRANOSYL) -α-D-GLUCURONOPYRANOSIDE, FROM WHEAT STRAW HOLOCELLULOSE AND SYNTHESIS OF ITS β-ISOMER |
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Canadian Journal of Chemistry,
Volume 31,
Issue 2,
1953,
Page 134-144
C. T. Bishop,
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摘要:
Extraction of wheat straw holocellulose with 4% potassium hydroxide removed a polysaccharide fraction containingD-xylose (77.2%),L-arabinose (6.9%), and uronic acid anhydride (7.9%). Hydrolysis of this polysaccharide with dilute acid produced a degraded polysaccharide which was precipitated by ethanol after removing freeD-xylose from the hydrolyzate by fermentation withHansenulasuaveolans. Prolonged hydrolysis of the degraded polysaccharide yielded an aldobiuronic acid which was shown to be 3-(xylopyranosyl)-α-D-glucuronopyranoside. The β-isomer of this compound was synthesized fromD-glucurone andD-xylose and its structure was confirmed by degradative studies after methylation. The enzyme β-glucuronidase did not hydrolyze the α- or β-isomers of this aldobiuronic acid.
ISSN:0008-4042
DOI:10.1139/v53-019
出版商:NRC Research Press
年代:1953
数据来源: NRC
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6. |
MICRODETERMINATION OF COBALT COLORIMETRICALLY AS THE 1-NITROSO-2-NAPHTHOL COMPLEX |
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Canadian Journal of Chemistry,
Volume 31,
Issue 2,
1953,
Page 145-149
W. E. Nichol,
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摘要:
An advantage of determining cobalt with 1-nitroso-2-naphthol is that the reagent is relatively stable and forms a very stable cobalt complex. Also this cobalt complex has maximum absorption in the visible spectrum which allows determination visually or with ordinary colorimeters.The procedure is based on decreasing the iron interference by the removal of part of the iron as phosphate and on a simple purification of the carbon tetrachloride solution of the 1-nitroso-2-naphthol cobalt complex which eliminates traces of palladium, iron, etc.The method has the same order of accuracy as theo-nitrosocresol method but preparation of reagents and the analysis in general require less time.
ISSN:0008-4042
DOI:10.1139/v53-020
出版商:NRC Research Press
年代:1953
数据来源: NRC
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7. |
THE DIFFUSION OF POLYISOBUTYLENE IN DIFFERENT SOLVENTS |
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Canadian Journal of Chemistry,
Volume 31,
Issue 2,
1953,
Page 150-152
C. Luner,
C. A. Winkler,
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摘要:
The diffusion coefficient of polyisobutylene inn-heptane has been found to decrease at first, then to increase with increasing molecular weight.
ISSN:0008-4042
DOI:10.1139/v53-021
出版商:NRC Research Press
年代:1953
数据来源: NRC
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8. |
SYNTHESIS OF ORGANIC DEUTERIUM COMPOUNDS: IV. METHYL-d3BROMIDE |
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Canadian Journal of Chemistry,
Volume 31,
Issue 2,
1953,
Page 153-157
B. Nolin,
L. C. Leitch,
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摘要:
Silver acetate-d3and bromine react readily in the dry state in a sealed tube to give methyl-d3bromide in high yield. This method is more convenient than the reduction of carbon dioxide to deuterated methyl alcohol with lithium aluminum deuteride, followed by the conversion of the alcohol into the halide, or other methods hitherto reported.
ISSN:0008-4042
DOI:10.1139/v53-022
出版商:NRC Research Press
年代:1953
数据来源: NRC
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9. |
PHOTOLYSIS OF ACETONE – HYDROGEN HLORIDE MIXTURES |
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Canadian Journal of Chemistry,
Volume 31,
Issue 2,
1953,
Page 158-170
R. J. Cvetanović,
E. W. R. Steacie,
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摘要:
The photolysis of acetone – hydrogen chloride mixtures has been investigated at 150 °C. and at room temperature. A strong suppression of ethane formation with a corresponding large increase in the formation of methane results from additions of relatively very small amounts of hydrogen chloride to acetone. The importance of the reactionsandhas been demonstrated. The collision yield of reaction (1) at 28 °C. is 2 × 10−4, and, therefore, the upper limit for E1is 5.1 kcal. per mole. The effects observed at 150° and 28° indicate that, on the assumption of a zero activation energy and a steric factor of unity for combination of methyl radicals, E1 = 2.1 ± 1 kcal. per mole, andP1is approximately 7 × 10−3.
ISSN:0008-4042
DOI:10.1139/v53-023
出版商:NRC Research Press
年代:1953
数据来源: NRC
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10. |
PHOTOLYSIS OF MIXTURES OF ACETONE AND SOME CHLORINATED METHANES |
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Canadian Journal of Chemistry,
Volume 31,
Issue 2,
1953,
Page 171-180
R. J. Cvetanović,
F. A. Raal,
E. W. R. Steacie,
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摘要:
Additions of carbon tetrachloride to acetone show in photolysis an apparent anomaly: methane formation is strongly increased and the formation of ethane correspondingly lowered. In this manner a hydrogen abstraction reaction is simulated. The cause of the anomaly and its bearing on the photolysis of acetone with other chlorinated methanes has been investigated.
ISSN:0008-4042
DOI:10.1139/v53-024
出版商:NRC Research Press
年代:1953
数据来源: NRC
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