International Journal of Radiation Applications and Instrumentation. Part C. Radiation Physics and Chemistry最新文献

筛选
英文 中文
Estimation of zirconium in Fe and Ti based alloys through formation of Zr-90m at 14.7 MeV neutrons 通过在14.7 MeV中子下形成Zr-90m来估计Fe和Ti基合金中的锆
G.R. Pansare, P.M. Dighe, V.N. Bhoraskar
{"title":"Estimation of zirconium in Fe and Ti based alloys through formation of Zr-90m at 14.7 MeV neutrons","authors":"G.R. Pansare,&nbsp;P.M. Dighe,&nbsp;V.N. Bhoraskar","doi":"10.1016/1359-0197(92)90027-D","DOIUrl":"10.1016/1359-0197(92)90027-D","url":null,"abstract":"<div><p>Neutrons of 14.7 MeV energy were bombarded on natural zirconium target and cross-section for formation of <sup>90m</sup>Zr through the nuclear reactions <sup>90</sup>Zr(n, n′)<sup>90m</sup>Zr and <sup>91</sup>Zr(n, 2n)<sup>90m</sup>Zr was measured. The cross-section value (σ = 470 ± 30 mb) was later on used for estimation of zirconium concentration, varying from a few hundred to a few thousand ppm, in iron and titanium based alloys.</p><p>An estimation sensitivity aroung 150 μg, in 1 g of sample weight, was achieved for both iron and titanium matrices which is much higher compared to an earlier reported value for geological samples.</p></div>","PeriodicalId":14262,"journal":{"name":"International Journal of Radiation Applications and Instrumentation. Part C. Radiation Physics and Chemistry","volume":"40 3","pages":"Pages 213-216"},"PeriodicalIF":0.0,"publicationDate":"1992-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/1359-0197(92)90027-D","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"81419227","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
Effect of 60Co-gamma radiation on the binding properties in furs 60co - γ辐射对毛皮结合性能的影响
R.K. Raina
{"title":"Effect of 60Co-gamma radiation on the binding properties in furs","authors":"R.K. Raina","doi":"10.1016/1359-0197(92)90032-B","DOIUrl":"10.1016/1359-0197(92)90032-B","url":null,"abstract":"<div><p>New Zealand white rabbit pelts were pickled by the usual procedure and were tanned with basic aluminium sulphate, basic chromium sulphate and their combinations. Tanned furs were irradiated with <sup>60</sup>Co-gamma radiations in the dose range of 5.0–114.0 kGy. The effect of radiation on the binding properties of various added substances like mineral tannins, fats, moisture and shrinkage temperature has been assessed by their comparison with the control samples. The results of these investigations show that radiation on furs causes detannage, increases the moisture and bound fat content and decreases the shrinkage temperature of the furs.</p></div>","PeriodicalId":14262,"journal":{"name":"International Journal of Radiation Applications and Instrumentation. Part C. Radiation Physics and Chemistry","volume":"40 3","pages":"Pages 245-247"},"PeriodicalIF":0.0,"publicationDate":"1992-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/1359-0197(92)90032-B","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"80735303","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
Paramagnetic molecular centers in the gamma-irradiated precipitates obtained in the system AlCl3-beta-alanine-NaOH alcl3 - β -丙氨酸- naoh体系中γ辐照沉淀物的顺磁分子中心
Takialdin A. Himdan, Vesna Noethig-Laslo, Halka Bilinski
{"title":"Paramagnetic molecular centers in the gamma-irradiated precipitates obtained in the system AlCl3-beta-alanine-NaOH","authors":"Takialdin A. Himdan,&nbsp;Vesna Noethig-Laslo,&nbsp;Halka Bilinski","doi":"10.1016/1359-0197(92)90029-F","DOIUrl":"10.1016/1359-0197(92)90029-F","url":null,"abstract":"<div><p>The presented results are the continuation of our work on paramagnetic molecular centers in the model clay compounds. Here it was attempted to incorporate β-alanine in the aluminium hydroxide matrix. A series of precipitates were prepared with the highest ratio of β-alanine/Al = 0.22 obtained at pH = 7.</p><p>X-ray diffraction analysis revealed in addition to amorphous precipitates, microcrystalline samples of four different X-ray patterns in nine precipitates, indicating variations in the structure of aluminium hydroxide matrix with incorporated β-alanine. Selected samples were exposed to γ-irradiation at 77 K, and at room temperature (293 K) in the presence and in the absence of air. In all the samples of amorphous structure no stable paramagnetic centers were determined by ESR after γ-irradiation in air.</p><p>In all samples of microcrystalline structure similar stable paramagnetic centers were determined by ESR after γ-irradiation in air and in the evacuated tubes. These paramagnetic centers that we were unable to identify due to the poor resolution of the lines in the ESR spectrum can be most probably ascribed to structural defects introduced into the aluminium hydroxide matrix by β-alanine.</p><p>In all amorphous samples γ-irradiated in the absence of air, the radical C̊H<sub>2</sub>CH<sub>2</sub>COOH formed by abstraction of amino group from the β-alanine was determined by ESR. The radical was unstable in air. Thus in the absence of air β-alanine may be considered as a storage site for the γ-irradiation energy in the amorphous aluminium hydroxides.</p></div>","PeriodicalId":14262,"journal":{"name":"International Journal of Radiation Applications and Instrumentation. Part C. Radiation Physics and Chemistry","volume":"40 3","pages":"Pages 225-231"},"PeriodicalIF":0.0,"publicationDate":"1992-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/1359-0197(92)90029-F","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"83338962","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
Solvent effects on the formation of cross-linking microspheres in γ-irridiated solutions 溶剂对γ-辐照溶液中交联微球形成的影响
Yukihiko Naka , Yukio Yamamoto , Koichiro Hayashi
{"title":"Solvent effects on the formation of cross-linking microspheres in γ-irridiated solutions","authors":"Yukihiko Naka ,&nbsp;Yukio Yamamoto ,&nbsp;Koichiro Hayashi","doi":"10.1016/1359-0197(92)90062-K","DOIUrl":"10.1016/1359-0197(92)90062-K","url":null,"abstract":"<div><p>Solvent effects on the formation of cross-linking microspheres by the radiation-induced polymerization are described. Polymerization of some bi- and tri-vinyl monomers in several organic solvents was tested. Diethylene glycol dimethacrylate (2G) is the unique monomer that gives microspheres. The distance between two vinyl groups of monomer molecules is one of the important factors for the formation of microspheres. The comparison of the solvent properties for the preparation of microspheres suggests that the forms of the monomer molecules in the solutions are also important, that is, the stretched form is favorable. Alcohols, except <em>t</em>-butanol, are not favorable as the solvents for the preparation of microspheres because of not only solubility but also an occurrence of the chain transfer reaction. The chain transfer reactions to the solvents and additives interfere with the formation of microspheres.</p></div>","PeriodicalId":14262,"journal":{"name":"International Journal of Radiation Applications and Instrumentation. Part C. Radiation Physics and Chemistry","volume":"40 2","pages":"Pages 83-88"},"PeriodicalIF":0.0,"publicationDate":"1992-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/1359-0197(92)90062-K","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"78855402","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
Polymerization of spin-casted epoxy films induced by electron beam or UV irradiation 电子束或紫外线辐照诱导自旋铸造环氧树脂膜聚合
I. Fujita , Y. Tanaka , J. Takezaki
{"title":"Polymerization of spin-casted epoxy films induced by electron beam or UV irradiation","authors":"I. Fujita ,&nbsp;Y. Tanaka ,&nbsp;J. Takezaki","doi":"10.1016/1359-0197(92)90075-Q","DOIUrl":"10.1016/1359-0197(92)90075-Q","url":null,"abstract":"<div><p>Polymerization of spin-casted epoxy oligomer resin-films was initiated by electron beam (EB) or UV irradiation and the conversion to polymer was studied as a function of the thickness of the film. The film thickness was varied from 1 to 25 μm. In the EB-irradiation, the number of oligomer molecules reacted per 100 eV of energy absorption (<em>G</em>-value) increased with increasing thickness up to 10 μm but did not change above this value. In the UV-irradiation, the <em>G</em>-value increased linearly with increasing film thickness. The result was explained by the difference in the penetrating power of the two radiations. The <em>G</em>-values and the quantum yields of the polymerization in the EB- and the UV-irradiations were compared on the basis of the same energy absorbed in the systems; it was found that the EB-irradiation was more effective than the UV-irradiation. Some anomalous polymerization behaviors were observed in thin, spin-casted films.</p></div>","PeriodicalId":14262,"journal":{"name":"International Journal of Radiation Applications and Instrumentation. Part C. Radiation Physics and Chemistry","volume":"40 2","pages":"Pages 161-165"},"PeriodicalIF":0.0,"publicationDate":"1992-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/1359-0197(92)90075-Q","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"85789523","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
Localization and migration of excess electron in aromatic substituted polyacetylenes in solution 芳香族取代聚乙炔溶液中多余电子的定位和迁移
Masaaki Ogasawara , Takashi Suganuma , Naonori Junke , Hitoshi Yamaoka , Hiroshi Yoshida
{"title":"Localization and migration of excess electron in aromatic substituted polyacetylenes in solution","authors":"Masaaki Ogasawara ,&nbsp;Takashi Suganuma ,&nbsp;Naonori Junke ,&nbsp;Hitoshi Yamaoka ,&nbsp;Hiroshi Yoshida","doi":"10.1016/1359-0197(92)90067-P","DOIUrl":"10.1016/1359-0197(92)90067-P","url":null,"abstract":"<div><p>Optical absorption spectra of radical anions of poly(1-phenyl-1-propyne)(PPPr) and poly(phenylacetylene)(PPA) were studied in 2-methyltetrahydrofuran (MTHF). The radical anions of the polymers were obtained by γ-radiolysis at 77 K (and 4 K) and pulse radiolysis at ambient temperature and 140 K. There were two different trapping sites for electrons in PPPr dissolved in MTHF. The electron produced by ionizing radiation was initially trapped by a site to form the radical anion which gave rise to an absorption spectrum with λ<sub>max</sub> at 390 and 560 nm and a shoulder at <em>ca</em> 800 nm. In liquids or warmed matrices, the spectrum relaxed to a new one which was similar to that of the radical anion of <em>trans-β</em>-methylstyrene, a model compound of the polymer. The result suggested that an electron trapped by a shallow site was ultimately localised on a deeper site of the size of a monomer unit. In contrast, the absorption spectrum of PPA<sup>-</sup> showed a strong IR band which was attributed to a dimer-type radical anion. It was concluded therefore that the excess electron was delocalized over two monomer units in PPA. The difference was interpreted in terms of the twisted main chain structure of PPPr arising from the repulsive interactions between bulky phenyl groups and methyl groups of the polymer.</p></div>","PeriodicalId":14262,"journal":{"name":"International Journal of Radiation Applications and Instrumentation. Part C. Radiation Physics and Chemistry","volume":"40 2","pages":"Pages 111-116"},"PeriodicalIF":0.0,"publicationDate":"1992-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/1359-0197(92)90067-P","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"78785080","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
Publications and patents of Koichiro Hayashi 林光一郎的出版物和专利
{"title":"Publications and patents of Koichiro Hayashi","authors":"","doi":"10.1016/1359-0197(92)90061-J","DOIUrl":"https://doi.org/10.1016/1359-0197(92)90061-J","url":null,"abstract":"","PeriodicalId":14262,"journal":{"name":"International Journal of Radiation Applications and Instrumentation. Part C. Radiation Physics and Chemistry","volume":"40 2","pages":"Pages vii-xvi"},"PeriodicalIF":0.0,"publicationDate":"1992-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/1359-0197(92)90061-J","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"136893456","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
On the degradation of polysilanes in solution. Flash photolysis and pulse radiolysis studies 聚硅烷在溶液中的降解研究。闪光光解和脉冲辐射解的研究
Carmen Peinado, Thomas Wollny, Wolfram Schnabel
{"title":"On the degradation of polysilanes in solution. Flash photolysis and pulse radiolysis studies","authors":"Carmen Peinado,&nbsp;Thomas Wollny,&nbsp;Wolfram Schnabel","doi":"10.1016/1359-0197(92)90065-N","DOIUrl":"10.1016/1359-0197(92)90065-N","url":null,"abstract":"<div><p>Polysilanes (catena-polysilicons) of the structure—SiR<sup>1</sup>R<sup>2</sup>—(R<sup>1</sup>, methyl; R<sup>2</sup>, phenyl, n-propyl, n-hexyl, β-phenethyl) and a copolymer (repeating units:—SiMe<sub>2</sub>—and—SiPhe<sub>2</sub>—) were irradiated with UV light (347 nm) or 15 MeV electrons. The dominant feature in both photolysis and radiolysis is main-chain scission. Typical quantum yields of main-chain scission determined by light scattering (LS) measurements are: φ(<em>S</em>) = 0.2 [poly(methyl-n-hexyl silane)] and φ(<em>S</em>) = 0.5 [poly(methyl-β-phenethyl silane)]. The radius of gyration <em>r</em><sub>G</sub> depends on <em>M</em><sub>W</sub> as <em>r</em><sub>G</sub> ∝ <em>M</em><sup><em>v</em></sup><sub>W</sub>; <em>v</em> = 0.5. Flash photolysis and pulse radiolysis studies in conjunction with optical absorption and LS measurements revealed that main-chain cleavage occurs very rapidly (τ&lt;20 ns). The resulting polymer fragments exhibit transient optical absorption probably originating from free radicals. The rate of decrease in LS intensity after the pulse corresponds to the rate of separation of fragments generated by main-chain cleavage. Regarding solutions of polysilane in liquids of bad solvent quality the rate of fragment separation is determined by the lifetime of contact pairs corresponding to physical interactions between polymer segments [at 23°C <em>ca</em> 100 μs in a 66/34 (v/v) mixture of 1,4-dioxane/1-propanol]. Moreover, it turned out that in benzene solution main-chain scission is sensitized by energy transfer from solvent to polysilane.</p></div>","PeriodicalId":14262,"journal":{"name":"International Journal of Radiation Applications and Instrumentation. Part C. Radiation Physics and Chemistry","volume":"40 2","pages":"Pages 101-106"},"PeriodicalIF":0.0,"publicationDate":"1992-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/1359-0197(92)90065-N","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"82962262","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
Elastic modulus formulae for a crosslinked network 交联网络的弹性模量公式
A. Charlesby
{"title":"Elastic modulus formulae for a crosslinked network","authors":"A. Charlesby","doi":"10.1016/1359-0197(92)90068-Q","DOIUrl":"10.1016/1359-0197(92)90068-Q","url":null,"abstract":"<div><p>The usual formula for the elastic modulus <em>E</em> of a crosslinked highly elastic network <em>E</em> = 3 <em>ρ</em>R<em>T</em>/<em>M</em><sub>c</sub> involves molecular weight between crosslinks <em>M</em><sub>c</sub>. It has to be modified by several factors such as the fraction not involved in any external stress and the initial molecular weight distribution. Several correction terms have been proposed. In this paper a fuller calculation is made for two initial molecular weight distributions, uniform and random, to see how far these corrections are valid. Even at high degrees of crosslinking a very significant proportion of the network does not participate in this elastic deformation.</p><p>It may appear preferable to relate the elastic modulus <em>E</em> to the number of effective segments between crosslinks, independent of their molecular weight <em>M</em><sub>c</sub><em>E</em> = 3<em>ρkTQ</em>(1 − <em>s</em><sup>2</sup>)<em>p</em> where <em>Q</em> is the number of crosslinked monomer units per unit volume, and (1 − <em>s</em><sup>2</sup>)<em>p</em> is a correction factor to allow for segments which are ineffective in an elastic deformation.</p></div>","PeriodicalId":14262,"journal":{"name":"International Journal of Radiation Applications and Instrumentation. Part C. Radiation Physics and Chemistry","volume":"40 2","pages":"Pages 117-120"},"PeriodicalIF":0.0,"publicationDate":"1992-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/1359-0197(92)90068-Q","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"75477185","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: 9
Effect of solid phase on the selectivity of alkyl radical formation by gamma-irradiation of branched alkanes 固相对支链烷烃γ辐照形成烷基自由基选择性的影响
Hitoshi Koizumi, Masatoshi Hashino, Tsuneki Ichikawa, Hiroshi Yoshida
{"title":"Effect of solid phase on the selectivity of alkyl radical formation by gamma-irradiation of branched alkanes","authors":"Hitoshi Koizumi,&nbsp;Masatoshi Hashino,&nbsp;Tsuneki Ichikawa,&nbsp;Hiroshi Yoshida","doi":"10.1016/1359-0197(92)90072-N","DOIUrl":"10.1016/1359-0197(92)90072-N","url":null,"abstract":"<div><p>ESR and electron spin echo measurements of alkyl radicals generated by γ-irradiation of glassy and crystalline branched alkanes C<sub>10</sub> ≈ C<sub>13</sub> have been carried out to elucidate the effect of molecular structure and solid phase on the selectivity of alkyl radical formation. Alkyl radicals generated and stabilized at 77 K in the glassy alkanes are secondary penultimate radicals. Tertiary radicals and secondary radicals other than the penultimate one are not generated either by hydrogen abstraction or from ionized or exited molecules. In the crystalline alkanes, however, a small amount of secondary internal radicals are generated in addition to the predominant formation of the secondary penultimate radicals. It is concluded that the detachment of C-H hydrogen preferentially takes place at the location where the motion of carbon atoms assisting the detachment of the C-H hydrogen easily occurs.</p></div>","PeriodicalId":14262,"journal":{"name":"International Journal of Radiation Applications and Instrumentation. Part C. Radiation Physics and Chemistry","volume":"40 2","pages":"Pages 145-150"},"PeriodicalIF":0.0,"publicationDate":"1992-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/1359-0197(92)90072-N","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"86850614","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
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
相关产品
×
本文献相关产品
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信