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  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 34 (1996), S. 349-356 
    ISSN: 0887-6266
    Keywords: phase separation ; thermoplastic-modified epoxies ; polyetherimide-modified epoxies ; Flory-Huggins equation ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The miscibility of polyetherimides (PEIs) with epoxy monomers based on diglycidylether of bisphenol-A (DGEBA), and with reactive mixtures based on stoichiometric amounts of DGEBA and an aromatic diamine (DA) {either 4,4′-diaminodiphenylsulfone (DDS) or 4,4′-methylenebis[3-chloro 2,6-diethylaniline] (MCDEA)}; was experimentally studied. Cloud-point curves (temperature vs. composition) are reported for PEI-DGEBA and PEI-DGEBA-DA initial mixtures. Cloud-point conversions are reported for the reactive mixtures, for various PEI amounts and polycondensation temperatures. A thermodynamic model based on the Flory-Huggins-Staverman approach, taking polydispersity of both components into account, was used to analyze the experimental information. A single relationship between the interaction parameter and temperature, χ(T), could fit experimental results of mixtures of two commercial PEIs with DGEBA. The addition of DDS led to a decrease in miscibility whereas MCDEA improved the initial miscibility. In both cases, the interaction parameter decreased with conversion, meaning that PEI was more compatible with oligomeric species than with the mixture of starting monomers. The phase separation process in initially miscible rubber- or thermoplastic-modified thermosetting polymers is the result of two factors: increase in the average molar size of the thermosetting oligomer (main driving force favoring demixing), and variation of the interaction parameter with conversion, which may act to increase or decrease the cloud-point conversion determined by the first factor. © 1996 John Wiley & Sons, Inc.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 29 (1995), S. 1545-1555 
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: This study was designed to evaluate the interfacial interactions between proteins and cells and a model surface which varied in its surface energy. The adsorption of proteins from single and binary solutions was studied using ellipsometry and the adhesion and spreading of L929 fibroblasts has been quantified using image analysis. The results demonstrated that after 24 h incubation, multilayer adsorbed fibrinogen appeared to produce a surface most conducive to cell adhesion and spreading on both the hydrophilic and hydrophobic regions of the material. Fibronectin on its own did not produce an optimal surface for cell spreading. Albumin produced a suitable surface for cell spreading on the hydrophilic part of the surface, but created a highly unsuitable surface on the hydrophobic region of the specimens. Competition between proteins for adsorption to the surface and changes in protein conformation was evident, particularly on the hydrophobic part of the material, and this was shown to influence cell adhesion and spreading. © 1995 John Wiley & Sons, Inc.
    Additional Material: 9 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 9 (1974), S. 418-421 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: When subjected to electron-impact, chloromethyl aryl sulphones (II, X = Cl) fragment predominantly by the loss of CH2Cl from the molecular ion followed by the loss of SO2 and in most cases the appropriate metastable peaks are present to confirm the transitions. In addition, alkyl-oxygen bond formation in the molecular ion was revealed by the presence of prominent peaks corresponding to the [R—φ-SO]+ ions. In most spectra no evidence for aryl-oxygen bond formation could be found and thus the presence of the chlorine atom was able to effectively reverse the direction of skeletal rearrangement reported for aryl methyl sulphones.
    Additional Material: 1 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 8 (1974), S. 175-178 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Upon electron-impact aryl methyl sulphones (I) rearranged to form aryl-oxygen bonds. The mode of fragmentation of the intermediate ester (II) to give [aryl O]+ or [aryl OH]+ ions was found to be markedly influenced by the nature of the aryl substituent.
    Additional Material: 2 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 9 (1974), S. 1217-1222 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A simple computerized electron distribution difference method has been developed using a conventional mass spectrometer and an on-line computer. Using the system, ionization potentials for various propyl halides were measured and found to agree well with photoionization data. The appearance potentials for [C3H7]+ agreed well with literature values, except for 1-propyl bromide and 1- propyliodide which gave values approximately 0.7 eV lower than previous reports. The results are interpreted to indicate threshold formation of the sec-propyl ion from all propul halides.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
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