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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 23 (1990), S. 1420-1429 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 23 (1990), S. 4696-4706 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Bulletin of mathematical biology 36 (1974), S. 17-28 
    ISSN: 1522-9602
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Mathematics
    Notes: Abstract Calculations based upon the membrane dipole model have been carried out and indicate the possibility of cooperative behavior during the membrane excitation process. An explicit expression is obtained for the critical electric field,E, which must be present to initiate the cooperative structural transition assumed to occur during membrane excitation. An hypothesis concerning the occurrence of two distinct phase transitions in the membrane resulting in the rapid influx of sodium ions and sodium ion inactivation, respectively, is presented.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 41 (1990), S. 2813-2828 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Several types of interpenetrating polymer networks (IPNs) from polyurethane/polymethyl methacrylate (LPU/PMMA) on the basis of lignin were prepared. All composites were judged to possess two phase morphology. The composition and the presence of crosslinking were found to influence the thermal and mechanical properties of the solvent-cast films. The mechanical properties were assessed by dynamic mechanical analysis and by tensile testing, and they were found to vary consistently with composition and the presence of crosslinks. The modulus behavior of the different IPNs could be explained by models which accounted for either dual phase continuity or phase inversion.
    Additional Material: 7 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 17 (1977), S. 647-651 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Multiblock , block copolymers of bisphenol-A-polycarbon ate and bisphenol-A-polysulfone were prepared by three different synthesis routes. The in situ method consisted of forming the polycarbonate block in the presence of hydroxyl terminated polysulfone oligorner. The coupled oligomer technique utilized phosgene to link up the two preformed oligomers to high molecular weight. In one case, a perfectly alternating block copolymer was formed by reacting a ∼9, 000 Mn chloroformate terminated polycarbonate with a ∼9, 000 Mn hydroxyl terminated polysulfone. Block sizes from ∼4, 000 to ∼26, 000 were investigated. The oligomers and copolymers were characterized by potentiometric titrations and UV end group analysis. Membrane osmometry and gel permeation chromatography were also employed. Dynamic mechanical behavior of solvent cast and compression molded films was assessed via rheovibron measurements. The copolymers were ductile and transparent and displayed essentially only a single intermediate glass transition temperature, that is, microphase separation was not observed. This is in contrast to simple physical blends of the homopolymers or oligomers, which are opaque and display two glass transition temperatures.
    Additional Material: 3 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 25 (1985), S. 934-941 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The equilibrium phase behavior of the partially miscible system polystyrene-polybutadiene-chloroform was studied at 25°C and 1 atm pressure by using gel permeation chromatography to analyze the conjugate phases. Three narrow molecular weight distribution samples of each polymer were used to provide nine examples of the system for study. The Flory-Huggins theory was used to determine the polymer-polymer interaction parameter χ23, When literature values of the two polymer-solvent interaction parameters χ12 and χ13 were used, the χ23 values generally were found to be negative and to show no distinct concentration dependence. No significant improvement was found when the literature value of only the polybutadiene-chloroform interaction parameter was used to simultaneously generate values of χ23 and χ12. Values of χ23 at the critical point, χ23,cr, were found to increase with increasing polymer concentration.
    Additional Material: 4 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 37 (1989), S. 2961-2971 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: A series of five fractions with number average molecular weights (M̄n) between 1500 and 10,000 daltons were isolated from a Kraft hydroxypropyl lignin (HPL). From 1H-NMR and UV analysis the chemical properties of the HPLs were found to vary slightly with molecular weight. The hydroxyl content decreased while the glass transition temperature (Tg) increased as the HPL molecular weight increased. The Fox-Flory equation adequately described the M̄n vs. Tg relationship. The HPL fractions were used as polyols for the preparation of solvent-cast polyurethane networks (PU) in film form. The Tg of the PUs increased from 40° to 120°C as the M̄n of the polyol rose from 1500 to 10,000 daltons. The molecular weight between crosslinks (M̄c) of the networks was determined by swelling. An observed decrease in M̄c with an increase in M̄n was related to the functionality of the system. The strength properties of films prepared from fractionated HPLs were superior to those prepared from nonfractionated HPLs.
    Additional Material: 4 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 36 (1988), S. 759-772 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: A series of polyurethane (PU) films was prepared from chain-extended hydroxypropyl lignins (CEHPL). In appearance, these films ranged from brittle and dark brown to rubbery and bronze. The thermal, mechanical, and network properties of these PUs were investigated by DMTA and DSC analysis. All films exhibited single Tg's which varied between -53° and 101°C, depending on lignin content. From swelling experiments, molecular weight between crosslinks (Mc) was determined and found to vary over 2.5 orders of magnitude. The Mc's were related to the change in Tg that accompanied network formation. Stress-strain experiments showed a variation in Young's modulus between 7 and 1300 MPa. Most of the variation in material properties was related to lignin content and to a lesser extent to diisocyanate type, hexamethylene diisocyanate, or toluene diisocyanate. The source of the CEHPL had no effect on the observed properties. From these results it was concluded that the properties of PUs can be controlled and engineered for a wide variety of practical uses.
    Additional Material: 8 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 25 (1987), S. 325-337 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Equilibrium phase diagrams of narrow molecular weight distribution samples of polystyrene and polyisoprene in the presence of toluene at 45°C and 1 atm pressure were established by means of gel permeation chromatography. The polymer-polymer interaction parameter was evaluated on the basis of the Flory-Huggins approach. The influence of polymer molecular weight and polymer-solvent interaction parameters on (i) the shape and location of the binodal curve, (ii) the location of the critical point, and (iii) the polymer-polymer interaction parameter was investigated.
    Additional Material: 3 Ill.
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  • 10
    ISSN: 0887-6266
    Keywords: soluble high-performance fully cyclized polyimides ; molecular weight characterization ; size exclusion chromatography (SEC) ; LALLS ; in-line viscosity detection ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Six different soluble high-performance aromatic polyimides, each prepared by solution imidization to three controlled average molecular weights, were analyzed by size exclusion chromatography (SEC) using on-line parallel coupled refractometric and viscometric detectors. N-methylpyrrolidone (NMP) with 0.06 M LiBr and NMP stirred over P2O5 were used as mobile phase for four of the polyimides; NMP with 0.06 M LiBr and NMP stirred over P2O5 were used as mobile phases for four of the polyimides; NMP with 0.06 M LiBr tetrahydrofuran (THF) and chloroform served as mobile phases for the other two polyimides. For all the samples the stationary phase in the SEC columns was cross-linked polystyrene beads. Molecular weight averages of the polyimides were calculated using universal SEC calibration with polystyrene standards in each solvent. The agreement of the calculated molecular weight averages in the different solvents confirms that the universal SEC calibrations are valid for these semiflexible polymers. There was good agreement with weightaverage molecular weights obtained by low-angle laser light scattering (LALLS) performed in pure NMP. Intrinsic viscosity and molecular weight data for a series of nine samples of one polyimide covering a Mw = 20,000-70,000 g mol-1 interval were treated to obtain Mark-Houwink-Sakurada constants. Unperturbed chain dimensions of this polyimide were obtained by application of the Stockmayer-Fixman extrapolation procedure to these data. ©1995 John Wiley & Sons, Inc.
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