International Journal for Radiation Physics and Chemistry最新文献

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Thermoluminescence isothermal decay in γ-irradiated CaSO4 : Dy phosphors—kinetics, and distribution of trap depths γ辐照CaSO4: Dy磷的热释光等温衰减动力学及俘获深度分布
International Journal for Radiation Physics and Chemistry Pub Date : 1976-01-01 Epub Date: 2002-10-09 DOI: 10.1016/0020-7055(76)90006-1
O. Fiorella, M. Mangia, E. Oliveri
{"title":"Thermoluminescence isothermal decay in γ-irradiated CaSO4 : Dy phosphors—kinetics, and distribution of trap depths","authors":"O. Fiorella,&nbsp;M. Mangia,&nbsp;E. Oliveri","doi":"10.1016/0020-7055(76)90006-1","DOIUrl":"https://doi.org/10.1016/0020-7055(76)90006-1","url":null,"abstract":"<div><p>In this paper our experiments on isothermal decay of thermoluminescence of the main peak of CaSO<sub>4</sub> : Dy phosphors at various temperatures and <sup>60</sup>Co γ doses are described. The decays are not monoexponential; however, as the shape of the decay curves at a same temperature is dose independent, first-order kinetics may be assumed. Consequently, the decay curves at 100 rad are broken down in exponential terms and for each term the decay constant and the related partial light sum are obtained. These results are interpreted, at first, by trying to associate with the peak a multilevel distribution of trap depths; however, the activation energies and the frequency factors for these levels are physically unacceptable. Subsequently, on the hypothesis of a continuous trap distribution, the decay curves are best fitted as a whole; in this way a frequency factor of 3 × 10<sup>12</sup> s<sup>−1</sup> and a trap distribution with an approximately gaussian main peak centred at about 1 &gt; ṡ37 eV and three other minor peaks are obtained. To check the consistency of the results, a theoretical glow curve is synthesized and a single peak fairly similar to the experimental one emerges.</p></div>","PeriodicalId":100688,"journal":{"name":"International Journal for Radiation Physics and Chemistry","volume":"8 4","pages":"Pages 441-447"},"PeriodicalIF":0.0,"publicationDate":"1976-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0020-7055(76)90006-1","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"91629348","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 23
Pulse radiolysis of aqueous solutions of tetraphenylphosphonium ions 脉冲辐射解四苯基磷离子水溶液
International Journal for Radiation Physics and Chemistry Pub Date : 1976-01-01 Epub Date: 2002-10-09 DOI: 10.1016/0020-7055(76)90017-6
H. Horii, S. Fujita, T. Mori, S. Taniguchi
{"title":"Pulse radiolysis of aqueous solutions of tetraphenylphosphonium ions","authors":"H. Horii,&nbsp;S. Fujita,&nbsp;T. Mori,&nbsp;S. Taniguchi","doi":"10.1016/0020-7055(76)90017-6","DOIUrl":"10.1016/0020-7055(76)90017-6","url":null,"abstract":"<div><p>The reactions of tetraphenylphosphonium ion (Ar<sub>4</sub>P<sup>+</sup>) with e<sub>aq</sub><sup>−</sup>, H atoms and OH radicals have been investigated. The absorption spectra of three transient species were obtained. Ar<sub>4</sub>P· radicals formed by the reaction: Ar<sub>4</sub>P<sup>+</sup> + e<sub>aq</sub><sup>−</sup> → Ar<sub>4</sub>P· have a maximum absorption at 305 nm [<em>ε</em><sub>305</sub> = (9400 ± 300) dm<sup>3</sup> mol<sup>−1</sup> cm<sup>−1</sup>] and decays by second-order kinetics with the rate constant 2<em>k</em> = (2·7 ±0·4) × 10<sup>9</sup> dm<sup>3</sup> mol<sup>−1</sup> s<sup>−1</sup>. H atoms and OH radicals form transient adducts to the phenyl groups of the Ar<sub>4</sub>P<sup>+</sup> ion with the rate constants of (1·5 ± 0·3) × 10<sup>9</sup> dm<sup>3</sup> mol<sup>−1</sup> s<sup>−1</sup> and (3·0±0·3) × 10<sup>9</sup> dm<sup>3</sup> mol<sup>−1</sup> s<sup>−1</sup>, respectively. Both adducts have broad absorption spectra at 300≈380 nm (<em>λ</em><sub>max</sub> = 340 nm) with the molar extinction coefficients <em>ε</em><sub>340</sub> = 5400±300 dm<sup>3</sup> mol<sup>−1</sup> cm<sup>−1</sup> for the H adduct and <em>ε</em><sub>340</sub> = 3500±200 dm<sup>3</sup> mol<sup>−1</sup> cm<sup>−1</sup> for the OH adduct.</p></div>","PeriodicalId":100688,"journal":{"name":"International Journal for Radiation Physics and Chemistry","volume":"8 4","pages":"Pages 521-522"},"PeriodicalIF":0.0,"publicationDate":"1976-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0020-7055(76)90017-6","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"88178588","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 8
Formation and role of excited states in radiolysis—A foreword 放射性溶解中激发态的形成和作用——前言
International Journal for Radiation Physics and Chemistry Pub Date : 1976-01-01 Epub Date: 2002-10-09 DOI: 10.1016/0020-7055(76)90055-3
Ajit Singh
{"title":"Formation and role of excited states in radiolysis—A foreword","authors":"Ajit Singh","doi":"10.1016/0020-7055(76)90055-3","DOIUrl":"10.1016/0020-7055(76)90055-3","url":null,"abstract":"","PeriodicalId":100688,"journal":{"name":"International Journal for Radiation Physics and Chemistry","volume":"8 1","pages":"Pages xi-xiii"},"PeriodicalIF":0.0,"publicationDate":"1976-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0020-7055(76)90055-3","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"79120749","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
γ-radiolysis of myo-inositol hexasulphate (free acid) in aqueous solution 六硫酸肌醇(游离酸)在水溶液中的γ-辐射分解
International Journal for Radiation Physics and Chemistry Pub Date : 1976-01-01 Epub Date: 2002-10-09 DOI: 10.1016/0020-7055(76)90021-8
M. Balakrishnan, W.J. Criddle, B.J. Jones
{"title":"γ-radiolysis of myo-inositol hexasulphate (free acid) in aqueous solution","authors":"M. Balakrishnan,&nbsp;W.J. Criddle,&nbsp;B.J. Jones","doi":"10.1016/0020-7055(76)90021-8","DOIUrl":"10.1016/0020-7055(76)90021-8","url":null,"abstract":"<div><p>The effects of <em>γ</em>-radiation on aqueous solutions of myo-inositol hexasulphate in the free acid form have been studied. The results have been explained on the basis of radical initiated chain processes which lead to the observed high <em>G</em>-values for the ultimate inorganic product namely the sulphate ion and to low hydrogen peroxide yields. In addition, steady-state competition procedures and pulse radiolysis experiments show that the reaction between the OH and the substrate is slow.</p></div>","PeriodicalId":100688,"journal":{"name":"International Journal for Radiation Physics and Chemistry","volume":"8 5","pages":"Pages 549-553"},"PeriodicalIF":0.0,"publicationDate":"1976-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0020-7055(76)90021-8","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"80972390","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Luminescence de recombinaison consecutive a la photoionisation d'une solution organique vitreuse-nouvelle methode experimentale 有机玻璃溶液光离子化后的连续复合发光-一种新的实验方法
International Journal for Radiation Physics and Chemistry Pub Date : 1976-01-01 Epub Date: 2002-10-09 DOI: 10.1016/0020-7055(76)90020-6
D. Ceccaldi
{"title":"Luminescence de recombinaison consecutive a la photoionisation d'une solution organique vitreuse-nouvelle methode experimentale","authors":"D. Ceccaldi","doi":"10.1016/0020-7055(76)90020-6","DOIUrl":"10.1016/0020-7055(76)90020-6","url":null,"abstract":"<div><p>In this paper, we describe a new experimental method which is used to determine the effect of temperature on the mechanisms related to the detrapping of electrons trapped in a glass. The studied samples are organic vitreous solutions of an aromatic molecule (TMPD) inside a non-polar glass (3-MP or MCH). The intensity of the isothermal luminescence (ITL) following the photoionization of the sample at 77K is increased when applying thermal jumps <em>ΔT</em>≲2K (the rise time is ⋍s).</p><p>A general kinetical theory is used to explain the shapes of the luminescence curves perturbed by thermal jumps. It is shown that the experimental observations can be explained in terms of a slow diffusion of the trapped electrons towards a tunneling detrapping zone. When applying a thermal jump <em>ΔT</em>, the intensity of luminescence is multiplied by <em>X</em> such as: <span><span><span><math><mtext>X = </mtext><mtext>exp</mtext><mtext> </mtext><mtext>ΔT</mtext><mtext>T</mtext><mtext>E</mtext><mtext>kT</mtext><mtext>+ Y</mtext><mtext>1+Y</mtext></math></span></span></span>.</p><p>This relationship is in good agreement with experience. The thermal detrapping activation energy <em>E</em> and the tunnelling effect ratio <em>Y</em> can be determined through this formula. The shapes of the kinetic curves at <em>T</em> = 77K and <em>T</em> = 77·50K are compared in the case of 3-MP glassy samples (near the glass transition, <em>T</em><sub><em>g</em></sub> = 77K). It is concluded that there is a slow diffusion of trapped electrons (as it was already shown); the diffusion activation energy (<em>E</em><sub><em>d</em></sub> = 0·65eV) is found to be very close to viscosity activation energy (<em>E</em> = 0·65eV) as given by Willard. This last result seems to support the hypothesis according to which the diffusion of trapped electrons is the consequence of the diffusion of the trapping cavities (at <em>T</em><sub><em>g</em></sub>).</p></div>","PeriodicalId":100688,"journal":{"name":"International Journal for Radiation Physics and Chemistry","volume":"8 5","pages":"Pages 539-548"},"PeriodicalIF":0.0,"publicationDate":"1976-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0020-7055(76)90020-6","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"73633173","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 2
Radiolysis of monocrystalline, liquid and aqueous solutions of methane sulphonic acid 甲烷磺酸单晶、液体和水溶液的辐射分解
International Journal for Radiation Physics and Chemistry Pub Date : 1976-01-01 Epub Date: 2002-10-09 DOI: 10.1016/0020-7055(76)90036-X
T.E. Eriksen, J. Lind, T. Gillbro
{"title":"Radiolysis of monocrystalline, liquid and aqueous solutions of methane sulphonic acid","authors":"T.E. Eriksen,&nbsp;J. Lind,&nbsp;T. Gillbro","doi":"10.1016/0020-7055(76)90036-X","DOIUrl":"10.1016/0020-7055(76)90036-X","url":null,"abstract":"<div><p>A study of the radiolysis of monocrystalline, liquid and aqueous solutions of methane sulphonic acid is reported. E.S.R.-measurements on γ-irradiated single crystals show that two radicals ·CH<sub>2</sub>SO<sub>2</sub>(OH) and CH<sub>3</sub>ŻSO<sub>2</sub>(OH)<sup>−</sup> are formed. Sulphonic acid-water mixtures were investigated by pulse radiolysis. A short-lived transient absorption with maximum at 450 nm is assigned to the radical ion CH<sub>3</sub>ŻSO<sub>2</sub>(OH)<sup>−</sup> (<em>ϵ</em> = 1740 dm<sup>3</sup> mol<sup>−1</sup> cm<sup>−1</sup>). Two longer-lived transient absorptions at 263 and 347 nm in concentrated solution were shifted to 242 and 332 nm respectively with increasing water concentration.</p><p>The 242/263 nm absorption is ascribed to the ·CH<sub>2</sub>SO<sub>3</sub><sup>−</sup> radical and its protonated form and the 332/347 nm absorption to the CH<sub>3</sub>SO<sub>2</sub>· radical formed by the decomposition of the CH<sub>3</sub>ŻSO<sub>2</sub>(OH)<sup>−</sup> radical ion. The interpretation of E.S.R. and optical spectra is based on the assumption of a hydrogen bonding structure of the sulphonic acid.</p></div>","PeriodicalId":100688,"journal":{"name":"International Journal for Radiation Physics and Chemistry","volume":"8 6","pages":"Pages 655-659"},"PeriodicalIF":0.0,"publicationDate":"1976-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0020-7055(76)90036-X","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"75129986","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Excitation in the radiation chemistry of inorganic gases 无机气体辐射化学中的激发
International Journal for Radiation Physics and Chemistry Pub Date : 1976-01-01 Epub Date: 2002-10-09 DOI: 10.1016/0020-7055(76)90061-9
C. Willis, A.W. Boyd
{"title":"Excitation in the radiation chemistry of inorganic gases","authors":"C. Willis,&nbsp;A.W. Boyd","doi":"10.1016/0020-7055(76)90061-9","DOIUrl":"10.1016/0020-7055(76)90061-9","url":null,"abstract":"<div><p>Gas phase radiation chemistry yield data and electron impact cross-section data are used to derive excitation mechanisms and to discuss the role of excited states in the radiation chemistry of O<sub>2</sub>, N<sub>2</sub>, N<sub>2</sub>O, CO, CO<sub>2</sub>, H<sub>2</sub>S, H<sub>2</sub>O and NH<sub>3</sub>. For each of these systems available cross-sections for ionization and neutral excitation are listed, together with relevant reaction rate data and a summary of the radiation chemistry studies at both high and low dose rates. In general, fairly complete mechanisms are derived and further tested by energy balance calculations. In order to present as complete a picture as possible, a summary of rates and products of ion-neutralization reactions is given at the end of the paper.</p></div>","PeriodicalId":100688,"journal":{"name":"International Journal for Radiation Physics and Chemistry","volume":"8 1","pages":"Pages 71-111"},"PeriodicalIF":0.0,"publicationDate":"1976-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0020-7055(76)90061-9","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"76932469","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 151
Note from the editor-in-chief 总编辑注
International Journal for Radiation Physics and Chemistry Pub Date : 1976-01-01 Epub Date: 2002-10-09 DOI: 10.1016/0020-7055(76)90053-X
A. Charlesby
{"title":"Note from the editor-in-chief","authors":"A. Charlesby","doi":"10.1016/0020-7055(76)90053-X","DOIUrl":"https://doi.org/10.1016/0020-7055(76)90053-X","url":null,"abstract":"","PeriodicalId":100688,"journal":{"name":"International Journal for Radiation Physics and Chemistry","volume":"8 1","pages":"Pages vii-viii"},"PeriodicalIF":0.0,"publicationDate":"1976-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0020-7055(76)90053-X","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"136548763","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Observation of excited states in the radiolysis of liquid hydrocarbons 液态烃辐射分解激发态的观察
International Journal for Radiation Physics and Chemistry Pub Date : 1976-01-01 Epub Date: 2002-10-09 DOI: 10.1016/0020-7055(76)90056-5
J.K. Thomas
{"title":"Observation of excited states in the radiolysis of liquid hydrocarbons","authors":"J.K. Thomas","doi":"10.1016/0020-7055(76)90056-5","DOIUrl":"10.1016/0020-7055(76)90056-5","url":null,"abstract":"<div><p>Various picosecond and nanosecond pulse radiolysis studies of excited states in alkane and erene liquids are described. In particular, the origin of the excited states is sought after. In alkanes ion neutralization gives rise to excited triplet states of solutes. Singlet energy transfer from excited alkanes to solutes gives rise to the excited singlet states of the solutes. In aromatic liquids both the excited singlet and triplet state of the solvent are observed, and energy transfer to solutes is readily established. The role of ion neutralization in the formation of excited states is proportionally less pronounced as the observed yield of ions is low. However, indirect experiments suggest that the ion neutralization reaction is too rapid for conventional observation, and even in arenes large yields of excited states are formed by ion neutralization.</p></div>","PeriodicalId":100688,"journal":{"name":"International Journal for Radiation Physics and Chemistry","volume":"8 1","pages":"Pages 1-12"},"PeriodicalIF":0.0,"publicationDate":"1976-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0020-7055(76)90056-5","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"82223142","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 29
Reactions of OH radicals with tris(1,10-phenanthroline)iron(II) studied by pulse radiolysis 脉冲辐射解法研究羟基自由基与三(1,10-菲罗啉)铁(II)的反应
International Journal for Radiation Physics and Chemistry Pub Date : 1976-01-01 DOI: 10.1016/0020-7055(76)90004-8
E. S. Floryan, P. Pagsberg
{"title":"Reactions of OH radicals with tris(1,10-phenanthroline)iron(II) studied by pulse radiolysis","authors":"E. S. Floryan, P. Pagsberg","doi":"10.1016/0020-7055(76)90004-8","DOIUrl":"https://doi.org/10.1016/0020-7055(76)90004-8","url":null,"abstract":"","PeriodicalId":100688,"journal":{"name":"International Journal for Radiation Physics and Chemistry","volume":"172 1","pages":"425-426"},"PeriodicalIF":0.0,"publicationDate":"1976-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"75466785","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 7
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