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61.
62.
Ezio Martuscelli 《Macromolecular Symposia》1996,104(1):59-64
Scientific, and technological developments of polymers will tend to increase their attitude to substitute different materials (ceramics, metals, glasses. wood). Substitution and penetration process of polymers will follow different routes mostly having as objective the realization of systems specific functions suitable then to be more and more market oriented. The possibilities to realize these goals will require strong efforts of basic and applied research. 相似文献
63.
Appropriately substituted allylic sulfides, sulfones, bromides, phosphonates, stannanes and peroxides, vinyl ethers and thionocarbonyl compounds are effective chain transfer agents in free radical polymerizations. These compounds function by a radical addition-fragmentation mechanism by which fragments derived from the chain transfer agents are installed at both ends of polymer chains. This provides a convenient method for preparing both mono- and di-end functional oligomers and polymers. Allylic peroxides fragment to give epoxy end groups while the other allylic compounds give rise to macromonomers by introducing terminal double bonds. 相似文献
64.
Barbara Immirzi Mario Malinconico Ezio Martuscelli Maria G. Volpe 《Macromolecular Symposia》1994,78(1):243-258
Reactive polymer blending of poly(β-hydroxybutyrate) (PHB) and its valerate copolymers (PHBV) are reported, following two different methodologies, namely polymerization of rubber inclusions in the preformed matrix or reactive melt blending of preformed polymers. As second phase, poly(butyl acrylate) (PBA) and polycaprolactone (PCL) are used. The results of spectroscopic, thermal, mechanical and morphological analysis indicate the existence of chemical interactions between the blend components. Such interactions are also responsible of a drastic change in the morphology. 相似文献
65.
Dynamic-mechanical data at various temperatures and for different blend compositions are presented for the system iPP/HOCP. The data, in all cases corresponding to the molten state, are relevant not only in view of the processing but especially because they allow some considerations on the blend structure. The data, looked at in different ways (namely the complex viscosity as a function both of frequency and temperature and in the form of Cole-Cole plots), seem to indicate that the system is always in a single phase. This appears somehow in contrast to some microscopic observations recently reported in literature: the discrepancy may be, however, also due to changes in the miscibility due to the applied stress. 相似文献
66.
Elisabetta Princi Silvia Vicini Enrico Pedemonte Noemi Proietti Donatella Capitani Anna Laura Segre Loredana D'Orazio Gennaro Gentile Carmen Polcaro Ezio Martuscelli 《Macromolecular Symposia》2004,218(1):343-352
Conversion of dihydroxyl groups to dialdehyde by periodate oxidation is a useful method widely used in derivatization of cellulose to activate the polymer to further reactions as grafting polymerization. To investigate the cellulose behavior at different level of oxidation and to better understand the influence of the crystallinity on the effects induced by oxidative reactions on different cellulose materials, linen and cotton textiles have been oxidized with periodate solutions in different conditions. Oxidized cellulose samples have been characterized by several techniques: solid-state 13C NMR, Wide Angle X-Ray diffraction, and SEM. Moreover the mechanical properties of the untreated and oxidized yarns have been evaluated by means of tensile tests, the oxidation degree has been measured by means of the hydroxylamine hydrochloride method. 相似文献
67.
68.
Ion trap tandem mass spectrometry study of dexamethasone transformation products on light activated TiO2 surface 总被引:3,自引:0,他引:3
Paola Calza Ezio Pelizzetti Mariacarla Brussino Claudio Baiocchi 《Journal of the American Society for Mass Spectrometry》2001,12(12):1286-1295
The photocatalytic transformation of dexamethasone and the formation of its intermediate compounds have been studied using titanium dioxide as a photocatalyst. The degradation of dexamethasone occurs easily through the formation of several hydroxy derivatives whose characterization has been made by HPLC/MS/MS. Even if both oxidative and reductive processes can be operating, only oxidative products have been identified in air saturated aqueous suspensions. A pattern of reaction pathways accounting for the observed intermediates is proposed. The obtained experimental evidence may be rationalized postulating the existence of a double initial mechanism. A single oxidation step resulting from the attack by one ·OH radical leading to the formation of five hydroxy-derivatives and a concomitant attack involving two ·OH radicals leading to the hydroxylation of the quinoid moiety of the molecule. 相似文献
69.
Salvatore Cabiddu Enzo Cadoni Stefana Melis Gioanna Gelli Maria Grazia Cabiddu Claudia Fattuoni Stefania De Montis Sandra Ianelli 《Tetrahedron》2001,57(52):10365-10375
The reaction of benzoxathiole-3-oxide with LDA in THF or THF/hexane or THF/HMPA gave a carbanion which was reacted with methyl iodide, aromatic aldehydes or carbon dioxide. The conformational stability (-diastereoselectivity) of the carbanion and the asymmetric induction due to the prochiral electrophiles (β-diastereoselectivity) was studied. The temperature and the solvent effects on the - and β-diastereoselectivity are discussed. 相似文献
70.