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1.
Summary A method for the determination of low-level radium isotopes in mineral and environmental water samples by alpha-spectrometry has been developed. Radium-225, which is in equilibrium with its mother 229Th, was used as a yield tracer. Radium were preconcentrated from water samples by coprecipitation with BaSO4and iron (III) hydroxide at pH 8-9 using ammonia solution, then isolated from uranium, thorium and iron using a Microthene-TOPO chromatography column at 8M HCl, separated from barium in a cation-exchange resin column using 0.05M 1,2-cyclohexylenedinitrilotetraacetic acid monohydrate at pH 8.5 as an eluant, and finally electrodeposited on a stainless steel disc in a medium of 0.17M (NH4)2C2O4at pH 2.6 and current density of 400 mA. cm-2, and counted bya-spectrometry. Optimum experimental conditions for radium separation, purification and electrodeposition have been studied and discussed in the paper. The lower limits of detection of the method are 0.11 mBq. l-1for 226Ra, 228Ra and 224Ra, respectively, if 2 l of water are analyzed. The method has been checked with a certified reference material IAEA-Soil-6 supplied by the International Atomic Energy Agency and reliable results were obtained. Eighteen water samples collected in Italy have been analyzed with the method, the mean radiochemical yields for radium were 86.2±6.5%. The obtained radium concentrations were in the range of 0.50-60.8 mBq. l-1for 226Ra, of 0.10-25.7 mBq. l-1for 228Ra, and of£LLD-7.97 mBq. l-1for 224Ra. The 228Ra/226Ra and 224Ra/226Ra ratios were in the range of 0.189-4.45 and£LLD-0.941, respectively.  相似文献   
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Powdered samples of cotton, flax and viscose from textile fibres were subjected to electron beam irradiation (20-400 KGy). ESR signals were observed after irradiation. The intensity of the signals depended on the administered dose and exhibited an exponential decay with time. The ESR spectra, whose pattern depended drastically on the crystallinity of the samples, indicated the simultaneous presence of at least three carbon-centred radical species. When the whole irradiated textile fibres were quenched in a solution of glycidyl methacrylate (GMA) a significant increase of the weight was observed, the increase being strongly dependent on the administered dose and on the time interval elapsed between irradiation and quenching. Spectroscopic characterisation evidenced that GMA acted as cellulose radicals scavenger on the unsubstituted carbon of the double bond and was covalently linked to the fibre through a new C-C bond while maintaining unaltered the ester and the epoxide groups, available for further derivatisations. Because irradiation of the whole textile fibres in the range 20-200 KGy does not result in significant degradation of the material, GMA quenching of fibres irradiated in this dose range may represent an attractive route to their functionalisation.  相似文献   
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A hydroxylactone ((1R,5S)‐1‐hydroxy‐3,6‐dioxabicyclo [3.2.1] octan‐2‐one, abbreviated as LAC) obtained from catalytic pyrolysis of cellulose was investigated as a monomer in the synthesis of polyesters by ring‐opening polymerization (ROP) with L ‐lactide. Although stannous octoate resulted inactive, ROP initiated by zirconium (IV) acetylacetonate afforded novel copolyesters from LAC and lactide mixtures in the bulk at 110 °C. Copolymers were obtained with different LAC content (from 19 to 45%) with a random microstructure as established by detailed NMR analysis. FTIR spectrometry confirmed the presence in the polymer chain of the OH groups originally present in LAC, which do not react during polymerization due to steric hindrance and inter/intramolecular hydrogen bonding. Reaction with trichloroacetylisocyanide proved that OH groups of the polyesters can be readily derivatized. The application of LAC as a comonomer enables the insertion of the alcohol functionality in polylactide avoiding protection/deprotection steps and potentially expanding the realm of biomaterials affordable from carbohydrate feedstock. © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 247–257, 2009  相似文献   
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1,2,3,4,6-Penta-O-galloyl-β-D-glucopyranose (PGG) is a polyphenolic compound found in substantial amounts in a number of medicinal herbs. We report (i) its conformational analysis by solution NMR and molecular dynamics calculation and (ii) theoretical study of its interaction with a model membrane bilayer. The galloyl groups B and E appear to play important roles in the interaction with the phospholipid bilayer.  相似文献   
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Irradiation of a number of different sutures largely employed in the clinical practice with either high energy electrons or with γ-rays followed by quenching with glycidyl methacrylate (GMA) conveniently led to derivatization through a radical-based process. The radicals involved were detected by means of ESR spectroscopy and were characterized on the basis of their ESR spectral parameters which were also found to be consistent with the hfs constants predicted by DFT calculations. Evidence of the GMA derivatization of the sutures was obtained via(13)C CP-MAS NMR spectroscopy, while its extent was evaluated gravimetrically.  相似文献   
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In this exploratory paper we propose a framework for the deduction apparatus of multi-valued logics based on the idea that a deduction apparatus has to be a tool to manage information on truth values and not directly truth values of the formulas. This is obtained by embedding the algebraic structure V defined by the set of truth values into a bilattice B. The intended interpretation is that the elements of B are pieces of information on the elements of V. The resulting formalisms are particularized in the framework of fuzzy logic programming. Since we see fuzzy control as a chapter of multi-valued logic programming, this suggests a new and powerful approach to fuzzy control based on positive and negative conditions.  相似文献   
10.
A short and efficient synthesis of novel tetracyclic Kynurenic acid analogues, isolated from chestnut honey, is described. The crucial step of the strategy was a MW-assisted cyclization of enamines of ethyl dioxohexahydropyrrolizine and 2,3-dioxooctahydroindolizine carboxylates to obtain 2,3,6,11b-tetrahydro-1H-pyrrolizino[2,1-b]quinoline-5,11-dione and 5,8,91,011,11a-hexahydroindolizino[2,1-b]quinoline-6,12-dione, respectively. Because of its modular nature, the synthetic strategy can have value as a general method for the preparation of compounds containing these new heterocyclic scaffolds.  相似文献   
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