Beta decay of 100/400 Zr produced in neutron-induced fission of natural uranium
- Authors: Kamoto, Thokozani
- Date: 2016
- Language: English
- Type: Thesis , Masters , MSc
- Identifier: http://hdl.handle.net/10962/3024 , vital:20353
- Description: Fission fragments, produced by neutron bombardment of natural uranium at the Physics Department, Jyväskylä, Finland, are studied in this work. The data had been sorted into 25 Y — y coincidence matrices which were then analysed. In this work we aimed to identify the fission products using Y-Y coincidence analysis and then study the beta-decay of some of the fission products. Sixteen fission products ranging from A = 94 to A = 136 were identified. Out of these fission products beta decay of the A = 100 (100/40 Zr – 100/41 Nb – 100/42 Mo) chain was studied in greater detail. We have also studied the variation of the relative intensities as a function of time of the 159-, 528-, 600-, 768-, 928- and 1502-keV Y-rav lines in 100/42 Mo and the profiles of the relative intensities have been modelled with the variation of the activity of 100/41 Nb against time. Configuration assignments of 100 Zr and 100/42 Mo are discussed.
- Full Text:
- Date Issued: 2016
- Authors: Kamoto, Thokozani
- Date: 2016
- Language: English
- Type: Thesis , Masters , MSc
- Identifier: http://hdl.handle.net/10962/3024 , vital:20353
- Description: Fission fragments, produced by neutron bombardment of natural uranium at the Physics Department, Jyväskylä, Finland, are studied in this work. The data had been sorted into 25 Y — y coincidence matrices which were then analysed. In this work we aimed to identify the fission products using Y-Y coincidence analysis and then study the beta-decay of some of the fission products. Sixteen fission products ranging from A = 94 to A = 136 were identified. Out of these fission products beta decay of the A = 100 (100/40 Zr – 100/41 Nb – 100/42 Mo) chain was studied in greater detail. We have also studied the variation of the relative intensities as a function of time of the 159-, 528-, 600-, 768-, 928- and 1502-keV Y-rav lines in 100/42 Mo and the profiles of the relative intensities have been modelled with the variation of the activity of 100/41 Nb against time. Configuration assignments of 100 Zr and 100/42 Mo are discussed.
- Full Text:
- Date Issued: 2016
In-beam spectroscopy of ⁷²Ge
- Authors: Henninger, Katharine Rose
- Date: 2012
- Subjects: Nuclear shapes , Hyperfine structure
- Language: English
- Type: Thesis , Masters , MSc
- Identifier: vital:5559 , http://hdl.handle.net/10962/d1018233
- Description: The high-spin states of the nucleus ⁷²Ge were populated via the ⁷°Zn(a,2n)⁷²Ge fusion-evaporation reaction at a beam-energy of 30 MeV. The ')'-decays were observed with the AFRODITE spectrometer array at iThemba LABS (Faure, South Africa). Twenty-seven new transitions, 18 new levels and 2 new bands were added to the ⁷²Ge level scheme, and several corrections were made to t he previously-known level scheme. Transitions were characterised using Directional Correlation from Oriented states (DCO) and polarisation measurements, and spin-parity assignments were made for 7 new levels. Spin and parity were also reassigned to a previously-known structure. One of the new bands was ident ified as part of an octupole-vibrational band. No tetrahedral states were observed in the scheme despite N = 40 and Z = 32 having been identified as tetrahedral magic numbers. The meaning of the new 14⁺ yrast level for the underlying structure of the ground state band is discussed
- Full Text:
- Date Issued: 2012
- Authors: Henninger, Katharine Rose
- Date: 2012
- Subjects: Nuclear shapes , Hyperfine structure
- Language: English
- Type: Thesis , Masters , MSc
- Identifier: vital:5559 , http://hdl.handle.net/10962/d1018233
- Description: The high-spin states of the nucleus ⁷²Ge were populated via the ⁷°Zn(a,2n)⁷²Ge fusion-evaporation reaction at a beam-energy of 30 MeV. The ')'-decays were observed with the AFRODITE spectrometer array at iThemba LABS (Faure, South Africa). Twenty-seven new transitions, 18 new levels and 2 new bands were added to the ⁷²Ge level scheme, and several corrections were made to t he previously-known level scheme. Transitions were characterised using Directional Correlation from Oriented states (DCO) and polarisation measurements, and spin-parity assignments were made for 7 new levels. Spin and parity were also reassigned to a previously-known structure. One of the new bands was ident ified as part of an octupole-vibrational band. No tetrahedral states were observed in the scheme despite N = 40 and Z = 32 having been identified as tetrahedral magic numbers. The meaning of the new 14⁺ yrast level for the underlying structure of the ground state band is discussed
- Full Text:
- Date Issued: 2012
Prototypes of black wattle tannins and their stereochemistry
- Authors: Drewes, Siegfried Ernst
- Date: 1963
- Subjects: Tannins -- Anthocyanidis Stereochemistry
- Language: English
- Type: Thesis , Doctoral , PhD
- Identifier: vital:4460 , http://hdl.handle.net/10962/d1011437
- Description: A number of interrelated flavonoid compounds, present in trace quantities in mature black wattle (Acacia mearnsii De Wild) bark, have been isolated and identified for the first time. They include a) the resorcinol-pyrogallol analogues, (+)-leuco-robinetinidin (7,5',4',5'-tetrahydroxyflavan-3,4-diol), dihydrorobinetin (7,5',4',5'-tetrahydroxyflavan-3-ol-4-one) and robtein (2',4',5,4,5- pentahydroxychalcone) and b) the resorcinol-catechol analogues, (+)-leuco-fisetinidin (7,3',4'-trihydroxyflavan-3,4-diol), fustin (7,3',4'-trihydroxyflavan-3-ol-4-one), (-)-fisetinidol (7,3',4'trihydroxyflavan- 3-ol), butein (2',4',3,4-tetrahydroxychalcone) and butin (7,5',4'-trihydroxyflavan-4-one). In addition, two flavonol glycosides, myricitrin (3,5,7,3',4',5'-hexahydroxyflavone-3-rhamnoside ) and quercitrin (5,5,7,5',4'-pentahydroxyflavone-3-rhamnoside), which belong to the phloroglucinol-pyrogallol and phloroglucinolcatechol class of flavonoids respectively, were isolated from immature bark. These represent the only glycosides isolated hitherto from wattle bark or heartwood extracts. Summary, p. i.
- Full Text:
- Date Issued: 1963
- Authors: Drewes, Siegfried Ernst
- Date: 1963
- Subjects: Tannins -- Anthocyanidis Stereochemistry
- Language: English
- Type: Thesis , Doctoral , PhD
- Identifier: vital:4460 , http://hdl.handle.net/10962/d1011437
- Description: A number of interrelated flavonoid compounds, present in trace quantities in mature black wattle (Acacia mearnsii De Wild) bark, have been isolated and identified for the first time. They include a) the resorcinol-pyrogallol analogues, (+)-leuco-robinetinidin (7,5',4',5'-tetrahydroxyflavan-3,4-diol), dihydrorobinetin (7,5',4',5'-tetrahydroxyflavan-3-ol-4-one) and robtein (2',4',5,4,5- pentahydroxychalcone) and b) the resorcinol-catechol analogues, (+)-leuco-fisetinidin (7,3',4'-trihydroxyflavan-3,4-diol), fustin (7,3',4'-trihydroxyflavan-3-ol-4-one), (-)-fisetinidol (7,3',4'trihydroxyflavan- 3-ol), butein (2',4',3,4-tetrahydroxychalcone) and butin (7,5',4'-trihydroxyflavan-4-one). In addition, two flavonol glycosides, myricitrin (3,5,7,3',4',5'-hexahydroxyflavone-3-rhamnoside ) and quercitrin (5,5,7,5',4'-pentahydroxyflavone-3-rhamnoside), which belong to the phloroglucinol-pyrogallol and phloroglucinolcatechol class of flavonoids respectively, were isolated from immature bark. These represent the only glycosides isolated hitherto from wattle bark or heartwood extracts. Summary, p. i.
- Full Text:
- Date Issued: 1963
A comparative study of the catechin components in the barks of wattle species related to Acacia Mernsii
- Authors: Maihs, Edwin Alfred
- Date: 1962
- Subjects: Wattles (Plants) Acacia mearnsii Acacia
- Language: English
- Type: Thesis , Doctoral , PhD
- Identifier: vital:4482 , http://hdl.handle.net/10962/d1012793
- Description: The distribution of flavonoid constituents in the barks of Acacia mearnsii De Wild.(black wattle) , A· decurens Willd. (green wattle), A. dealbata Link.(silver wattle) and A. pycnantha Benth.(golden wattle) has been studied. Bark extracts of the four wattle species have been fractionated into low molecular weight fractions containing mainly catechins and other low molecular weight constituents, and high molecular weight fractions containing the bulk of the polymerized tannins. The low molecular weight fractions have been further fractionated by "preparative paper chromatography". (-)-Robinetinidol, (-)-7:3': 4': 5'-tetrahydroxy flavan- 3-ol, a new naturally occurring catechin, (+)-catechin and (+)-gallocatechin have been isolated from the barks of A. mearnsii, A. dealbata and A. pycnantha. (-)-Epicatechin and (-)-epigallocatechin have been identified in the bark extracts of A. dealbata and A. pycnantha, but appeared to be absent in the barks of A. mearnsii and A. decurrens. (-)-Epicatechin has been isolated fron A. dealbata, and both (-}-epicatechin and (-)-epigallocatechin were isolated from A. pycnantha. (-)-Epicatechin gallate, (-)-epigallocatechin gallate and gallic acid were isolated from A. pycnantha only. These three constituents appeared to be absent in the barks of the three other wattle species. (-)-Epigallocatechin, (-)-epicatechin gallate and (-)-epigallocatechin gallate which were not available for direct comparison, were subsequently isolated from green tea where they are present as major phenolic constituents. A method for the quantitative estimation of polyphenolic substances on two dimensional paper chromatograms has been developed, and a photoelectric densitometer constructed. Two spray reagents, ammoniacal silver nitrate and bisdiazotised benzidine, were found to give straight line relationships of instrument deflection against log concentration for flavonoid substances. This estimation method for the first time supplied means for a detailed study of the concentration of catechin constituents in the bark extracts of A. mearnsii, A. decurrens, A. dealbata, A. pycnantha and of A. mearnsii x A. decurrens hybrids. The concentration of catechin constituents has been shown to vary considerably between species whereas variation within species was small. In the latter respect silver wattle is an exception. Taxonomic significance may possibly be attached to the distribution of catechin constituents in the bark of the four Acacia species. The concentration of (-)-robinetinidol, which appears to be the characteristic compound of these Acacias, progressively decreases in the sequence black-, black x green hybrid, green-, silver- and golden wattle, while the number of catechin constituents of the "phloroglucinol series" increases in the same sequence. It thus appears, that by the examination of their bark components, a differentiation between species of a subgenera may be possible. Two tannins, constituents D and B, which are related to the leuco-anthocyanidins (flavan-3:4-diols) have been found in the barks of the four wattle species. One of the two, constituent D, was isolated in a pure form from the barks of A. mearnsii and A. pycnantha. Constituent D was found to generate robinetinidin and an orange pigment, the structure of which has not yet been fully identified. Compound D and its acetyl- and methoxyl derivatives did not crystallize. From the results of alkaline-, acidic- and enzymatic degradations, colour reactions and light-absorption studies, combustion analysis of the compound and its derivatives and molecular weight estimations, constituent D is surmised to be a dimer of 7:3': 4': 5'-tetrahydroxyflavan-3:4-diol (leuco-robinetinidin), The isolation of this complex leuco-anthocyanidin tannin represents the first isolation of a flavonoid tannin from commercial vegetable tannin sources. The second tannin obtained from the bark of A.mearnsii, "constituent B" appears to consist of two overlapping substances, which have not yet been separated. The tannin (B) was found to have an average molecular weight of 676 and it is considered likely that both substances may be dimolecular. On heating with mineral acid robinetinidin, fisetinidin and an orange pigment are generated, the pigment being identical with the pigment generated from constituent D. It may therefore be assumed that "Constituent B" consists of a mixture of complex leuco-robinetinidins and leucofisetinidins. The distribution of complex leuco-anthocyanidins in the bark extracts of Acacia mearnsii, A. decurrens, A. dealbata and A. pycnantha has been examined. A correlation between the distribution of leuco-anthocyanidins in the bark of the four wattle species, and accepted systematics, does not, apparently, exist.
- Full Text:
- Date Issued: 1962
- Authors: Maihs, Edwin Alfred
- Date: 1962
- Subjects: Wattles (Plants) Acacia mearnsii Acacia
- Language: English
- Type: Thesis , Doctoral , PhD
- Identifier: vital:4482 , http://hdl.handle.net/10962/d1012793
- Description: The distribution of flavonoid constituents in the barks of Acacia mearnsii De Wild.(black wattle) , A· decurens Willd. (green wattle), A. dealbata Link.(silver wattle) and A. pycnantha Benth.(golden wattle) has been studied. Bark extracts of the four wattle species have been fractionated into low molecular weight fractions containing mainly catechins and other low molecular weight constituents, and high molecular weight fractions containing the bulk of the polymerized tannins. The low molecular weight fractions have been further fractionated by "preparative paper chromatography". (-)-Robinetinidol, (-)-7:3': 4': 5'-tetrahydroxy flavan- 3-ol, a new naturally occurring catechin, (+)-catechin and (+)-gallocatechin have been isolated from the barks of A. mearnsii, A. dealbata and A. pycnantha. (-)-Epicatechin and (-)-epigallocatechin have been identified in the bark extracts of A. dealbata and A. pycnantha, but appeared to be absent in the barks of A. mearnsii and A. decurrens. (-)-Epicatechin has been isolated fron A. dealbata, and both (-}-epicatechin and (-)-epigallocatechin were isolated from A. pycnantha. (-)-Epicatechin gallate, (-)-epigallocatechin gallate and gallic acid were isolated from A. pycnantha only. These three constituents appeared to be absent in the barks of the three other wattle species. (-)-Epigallocatechin, (-)-epicatechin gallate and (-)-epigallocatechin gallate which were not available for direct comparison, were subsequently isolated from green tea where they are present as major phenolic constituents. A method for the quantitative estimation of polyphenolic substances on two dimensional paper chromatograms has been developed, and a photoelectric densitometer constructed. Two spray reagents, ammoniacal silver nitrate and bisdiazotised benzidine, were found to give straight line relationships of instrument deflection against log concentration for flavonoid substances. This estimation method for the first time supplied means for a detailed study of the concentration of catechin constituents in the bark extracts of A. mearnsii, A. decurrens, A. dealbata, A. pycnantha and of A. mearnsii x A. decurrens hybrids. The concentration of catechin constituents has been shown to vary considerably between species whereas variation within species was small. In the latter respect silver wattle is an exception. Taxonomic significance may possibly be attached to the distribution of catechin constituents in the bark of the four Acacia species. The concentration of (-)-robinetinidol, which appears to be the characteristic compound of these Acacias, progressively decreases in the sequence black-, black x green hybrid, green-, silver- and golden wattle, while the number of catechin constituents of the "phloroglucinol series" increases in the same sequence. It thus appears, that by the examination of their bark components, a differentiation between species of a subgenera may be possible. Two tannins, constituents D and B, which are related to the leuco-anthocyanidins (flavan-3:4-diols) have been found in the barks of the four wattle species. One of the two, constituent D, was isolated in a pure form from the barks of A. mearnsii and A. pycnantha. Constituent D was found to generate robinetinidin and an orange pigment, the structure of which has not yet been fully identified. Compound D and its acetyl- and methoxyl derivatives did not crystallize. From the results of alkaline-, acidic- and enzymatic degradations, colour reactions and light-absorption studies, combustion analysis of the compound and its derivatives and molecular weight estimations, constituent D is surmised to be a dimer of 7:3': 4': 5'-tetrahydroxyflavan-3:4-diol (leuco-robinetinidin), The isolation of this complex leuco-anthocyanidin tannin represents the first isolation of a flavonoid tannin from commercial vegetable tannin sources. The second tannin obtained from the bark of A.mearnsii, "constituent B" appears to consist of two overlapping substances, which have not yet been separated. The tannin (B) was found to have an average molecular weight of 676 and it is considered likely that both substances may be dimolecular. On heating with mineral acid robinetinidin, fisetinidin and an orange pigment are generated, the pigment being identical with the pigment generated from constituent D. It may therefore be assumed that "Constituent B" consists of a mixture of complex leuco-robinetinidins and leucofisetinidins. The distribution of complex leuco-anthocyanidins in the bark extracts of Acacia mearnsii, A. decurrens, A. dealbata and A. pycnantha has been examined. A correlation between the distribution of leuco-anthocyanidins in the bark of the four wattle species, and accepted systematics, does not, apparently, exist.
- Full Text:
- Date Issued: 1962
Guibourtacacidin: a new Leuco-anthocyanidin from Rhodesian copalwood; (Guibourtia coleosperma)
- Authors: De Bruyn, Guustaaf Cornelis
- Date: 1962
- Subjects: Phanerogams , Angiosperms , Flavonoids , Anthocyanidins
- Language: English
- Type: Thesis , Masters , MSc
- Identifier: vital:4459 , http://hdl.handle.net/10962/d1011043
- Description: A new leuco-anthocyanidin, (+)-7,4'dihydroxyflavan- 3:4-diol has been isolated from the heartwood of Guibourtia coleosperma. The heartwood extractives were fractionated by enrichment procedures involving fractional precipitation and Craig partitioning, to give a high RF (subscript) low molecular weight fraction containing the above leuco -anthocyanidin. This was further fractionated by "preparative" paper chromatography . The leuco-anthocyanidin was amorphous and present in low proportion (0.004%) in the wood. On boiling with alcoholic hydrochloric acid the compound gave an anthocyanidin which was identified as 3,7,4'-trihydroxyflavylium chloride. The degradation products formed by alkali fusion, on a micro-scale, were resorcinol and ♭-resorcylic acid, and also p (underscore)-hydroxybenzoic acid. This indicated resorcinol and phenol A and B nuclei respectively. The formation of amorphous dimethyl ether and tetra-acetoxy derivatives indicated two phenolic and two alcoholic hydroxyl groups. The above indicates that the compound was 7,4'-dihydroxyflavan- 3:4- diol and a molecular weight estimation showed it to be monomeric. Comparison of the infrared absorption spectra of the natural dimethyl ether with synthetic (±) dimethoxyflavan- 3:4-diol, to which a tentative 2:3- trans- 3:4-cis conformation had been assigned (Phatak and Kulkarni 94), showed close identity. Crystalline (±)-7, 4 '-dihydroxyflavan- 3:4 - diol was synthesised by catalytic hydrogenation over platinum oxide of the corresponoing (±) -7,4'-dihydroxyflavanonol. The flavanonol was synthesised by sodium hyposulphite reduction of the 7,4 ' -dihydroxyflavonol. The infrared absorption spectra of the natural and synthetic diols were similar but not identical. Chromatographic evidence showed the apparent identity of the synthetic and natural flavan- 3:4- diols, and two possible configurations were assigned for the natural flavan-3:4-diol. The new leuco-anthocyanidin was observed to form an O(underscore)-ethyl ether derivative on manipulation in ethanol. A monomeric leuco- fisetinidin from the heartwood was identified, by two dimensional paper chromatography, as (+) - mollisacacidin. The condensed tannins found also in the heartwood of G.(underscore)- coleosperma appear to be polymeric forms of leuco - fisetinidin and leuco - guibourtinidin. These polymeric tannins form a large proportion of the heartwood extractives and furnish high yields of fisetinidin and guibourtinidin chlorides on boiling with alcoholic hydrochloric acid. Examination of some other members of the Guibourtia spp . by paper chromatography showed that only G (underscore). coleosperma contained the new leuco - anthocyanidin as well as a leuco - fisetinidin. G. (underscore) tessmannii and G. (underscore) demeusii heartwoods contained only leuco-fisetinidin and the related polymers and a close chemical relationship to G.(underscore) coleosperma is thus apparent. G.(underscore) arnoldiana on the other hand is not chemically interrelated with the above members since it appeared to contain only leuco - cyanidin. (±) - 7,4 ' -Dihydroxyflavan- 4-ol was synthesised by hydrogenation of the corresponding flavanone over platinum oxide. Observations were made regarding its reddenig and ease of condensation.
- Full Text:
- Date Issued: 1962
- Authors: De Bruyn, Guustaaf Cornelis
- Date: 1962
- Subjects: Phanerogams , Angiosperms , Flavonoids , Anthocyanidins
- Language: English
- Type: Thesis , Masters , MSc
- Identifier: vital:4459 , http://hdl.handle.net/10962/d1011043
- Description: A new leuco-anthocyanidin, (+)-7,4'dihydroxyflavan- 3:4-diol has been isolated from the heartwood of Guibourtia coleosperma. The heartwood extractives were fractionated by enrichment procedures involving fractional precipitation and Craig partitioning, to give a high RF (subscript) low molecular weight fraction containing the above leuco -anthocyanidin. This was further fractionated by "preparative" paper chromatography . The leuco-anthocyanidin was amorphous and present in low proportion (0.004%) in the wood. On boiling with alcoholic hydrochloric acid the compound gave an anthocyanidin which was identified as 3,7,4'-trihydroxyflavylium chloride. The degradation products formed by alkali fusion, on a micro-scale, were resorcinol and ♭-resorcylic acid, and also p (underscore)-hydroxybenzoic acid. This indicated resorcinol and phenol A and B nuclei respectively. The formation of amorphous dimethyl ether and tetra-acetoxy derivatives indicated two phenolic and two alcoholic hydroxyl groups. The above indicates that the compound was 7,4'-dihydroxyflavan- 3:4- diol and a molecular weight estimation showed it to be monomeric. Comparison of the infrared absorption spectra of the natural dimethyl ether with synthetic (±) dimethoxyflavan- 3:4-diol, to which a tentative 2:3- trans- 3:4-cis conformation had been assigned (Phatak and Kulkarni 94), showed close identity. Crystalline (±)-7, 4 '-dihydroxyflavan- 3:4 - diol was synthesised by catalytic hydrogenation over platinum oxide of the corresponoing (±) -7,4'-dihydroxyflavanonol. The flavanonol was synthesised by sodium hyposulphite reduction of the 7,4 ' -dihydroxyflavonol. The infrared absorption spectra of the natural and synthetic diols were similar but not identical. Chromatographic evidence showed the apparent identity of the synthetic and natural flavan- 3:4- diols, and two possible configurations were assigned for the natural flavan-3:4-diol. The new leuco-anthocyanidin was observed to form an O(underscore)-ethyl ether derivative on manipulation in ethanol. A monomeric leuco- fisetinidin from the heartwood was identified, by two dimensional paper chromatography, as (+) - mollisacacidin. The condensed tannins found also in the heartwood of G.(underscore)- coleosperma appear to be polymeric forms of leuco - fisetinidin and leuco - guibourtinidin. These polymeric tannins form a large proportion of the heartwood extractives and furnish high yields of fisetinidin and guibourtinidin chlorides on boiling with alcoholic hydrochloric acid. Examination of some other members of the Guibourtia spp . by paper chromatography showed that only G (underscore). coleosperma contained the new leuco - anthocyanidin as well as a leuco - fisetinidin. G. (underscore) tessmannii and G. (underscore) demeusii heartwoods contained only leuco-fisetinidin and the related polymers and a close chemical relationship to G.(underscore) coleosperma is thus apparent. G.(underscore) arnoldiana on the other hand is not chemically interrelated with the above members since it appeared to contain only leuco - cyanidin. (±) - 7,4 ' -Dihydroxyflavan- 4-ol was synthesised by hydrogenation of the corresponding flavanone over platinum oxide. Observations were made regarding its reddenig and ease of condensation.
- Full Text:
- Date Issued: 1962
- «
- ‹
- 1
- ›
- »