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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Colloid & polymer science 278 (2000), S. 187-194 
    ISSN: 1435-1536
    Keywords: Key words Poly(vinyl alcohol) ; Borax ; Dynamic light scattering ; Viscoelasticity
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract  The reentrant behavior of Poly(vinyl alcohol) (PVA)–borax aqueous semidilute solutions with a PVA concentration of 20 g/l and borax concentrations varies from 0.0 to 0.20 M was investigated using dynamic light scattering (DLS) and dynamic viscoelastic measurements. Two (fast and slow modes) and three (fast, middle, and slow) relaxation modes of PVA semidilute aqueous solutions without and with the presence of borax, respectively, were observed from DLS measurements. The fast and middle relaxation modes were q 2-dependent (q is the scattering vector) characteristic of diffusive behavior; however, the slow modes were q 3-dependent, characteristic of intraparticle dynamics. The experimental results showed that the slow relaxation mode dominates the DLS relaxation. The DLS slow mode relaxation time, τs, and the viscoelastic modulus G′(ω) and G′′(ω) data had a similar trend and demonstrated reentrant behavior as the borax concentration was increased from 0.0 to 0.20 M, i.e. τs, G′(ω), and G′′(ω) fluctuated with increasing borax concentration. The excluded-volume effect of polymers, charge repulsion among borate ions bound on PVA molecules, and intermolecular cross-linking didiol–borate complexation caused an expansion of the polymer chain; however, the screening effect of free Na+ ions on the negative charge of the borate ions bound on PVA and intramolecular cross-linking didiol–borate complexation led to a shrinkage of the polymer chain. The reentrant behavior was the consequence of the balance between expansion and shrinkage of the PVA–borate complex.
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of polymer research 5 (1998), S. 67-76 
    ISSN: 1572-8935
    Keywords: Poly(vinyl alcohol) ; Borax ; Dynamic light scattering ; Dilute solutions
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Abstract Poly(vinyl alcohol)-borate (PVA-borate) complexes in dilute aqueous solutions were investigated by dynamic light scattering (DLS). Two relaxation modes obtained, were scattering vector-q2 dependent and diffusive. The amplitude of slow mode was independent of borax concentration. In the very dilute PVA concentration regime ( [PVA] 〈 5 g/L), the PVA di-diol-borate complexation was dominated by intra-molecular reaction, and the fast mode correlation length ςf which corresponds to the polymer chain dimension increased rapidly with borax concentrations lower than 0.06 M, and reached an asymptote in the higher borax concentration regime. However, for a dilute PVA aqueous solution with higher PVA content (i.e., [PVA] = 9 g/L), both intra-and inter-molecular PVA di-diol-borate complexations might happen. The chain expansion and shrinkage of PVA-borate complex with increasing borax concentration was observed due to the balance between the electrostatic repulsion of the charged diol-borate complexes and the intra-molecular crosslink induced by the intra-molecular di-diol-borate complexation.
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  • 3
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995), S. 1884-1894 
    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: Two series of unsaturated polyesters (UPE from isophthalic acid, fumaric acid, and propylene glycol) were prepared. In series-A resins, UPEs wee thickened with isocyanate-terminated saturated aliphatic polyestes, i.e., an isocyanate-terminated polycaprolactone diol (PE-di-OL), through reaction of the isocyanate group with the hydroxyl group of the UPE. In series-B resins, the UPEs were mixed with saturated aliphatic polyesters i.e., PE-di-OL. The curing reaction of these two series of UPEs with styrene was studied by using differential scanning calorimetry (DSC) and gel permeation chromatography (GPC). The DSC data show that for a fixed PE-di-OL molecular weight, the curing reaction rate of series-A UPE is faster than that of series-B UPE. The variation of microgel size during curing ws studied by GPC. These results revealed that microgel formation has a great effect on the kinetics of cure for the unsaturated polyester-styrene system. The curing of these two series of UPEs is found to strongly depend on the compatibility of the components in the curing system.
    Additional Material: 9 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Macromolecular Chemistry and Physics 196 (1995), S. 1307-1318 
    ISSN: 1022-1352
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A series of unsaturated polyesters were synthesized with various chemical structures and molecular weights. The effects of molecular weight and degree of unsaturation on the curing reaction of these polyesters with styrene were studied by means of dynamic light scattering and differential scanning calorimetry. Two modes of size distribution of the microgel particles formed during the curing reaction were found from dynamic light scattering data. The small particles consist of primary unsaturated polyester molecules. The large ones consists of microgel particles formed by linking adjacent polyester molecules. The size and structure of the microgel particles depend strongly on the polymer chain length and the number of vinyl groups in each unsaturated polyester chain. The experimental results of this study revealed that microgel formation has a great effect on the curing reaction of unsaturated polyester resins.
    Additional Material: 6 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 57 (1995), S. 7-23 
    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: The effect of low-profile additives (LPA), i.e., poly(vinyl acetate) (PVAC) and poly(methyl methacrylate) (PMMA), on the curing reaction of unsaturated polyester (UPE) resins was studied by gel permeation chromatography (GPC) and differential scanning calorimetry (DSC). The curing reaction profiles were determined by DSC, while GPC was used to investigate the variation of the sizes of microgel particles during the early stage of curing reaction in UPE-styrene resins. The DSC experimental results indicated that the curing reaction rate decreased as the concentration of LPA increased. At a fixed LPA concentration, the curing reaction rate was slower for resins mixed with LPA possessing worse compatibility with UPE resins. During the early stage of curing reaction, the size and structure of the UPE microgels formation strongly depended on the concentration of LPA and also on the compatibility of the components in the curing system. The experimental results of this study revealed that the concentration of LPA and the compatibility of LPA with UPE resins had a strong influence on the polyester microgel formation and the curing behavior. © 1995 John Wiley & Sons, Inc.
    Additional Material: 8 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 61 (1996), S. 2423-2435 
    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: Poly(ether sulfone imide)s (PEI) with molecular weight Mn ∼ 104 were synthesized from 3,3′,4,4′-benzophenone tetracarboxylic dianhydride and amine terminated poly(ether sulfone) having molecular weights ranging from Mn ∼ 400 to Mn ∼ 4000. Thus, the PEIs had the same molecular weight but various imide and ether sulfone contents. The PEIs were mixed with a stoichiometric mixture of diglycidyl ether bis-phenol-A (DGEBA)/diamino diphenyl sulfone (DDS). The effect of PEI on the curing reaction of DGEBA/DDS and the morphology of the polymer blend were studied by differential scanning calorimetry (DSC) and optical microscopy. In the DGEBA/DDS/PEI blend with a fixed PEI molecular weight and PEI concentration but with various imide content, the experimental data revealed the PEI with a higher content of ether sulfone had a lower Tg and a better compatibility with solvents and epoxy resins; the curing reaction rate of DGEBA/DDS/PEI was faster for PEI with a higher imide content; the DSC data of cured DGEBA/DDS/PEI showed two Tgs, indicating phase separation between PEI and cured epoxy resins; and the data of optical microscopy showed that the compatibility of PEI with epoxy resins increased with the content of ether sulfone in PEI. © 1996 John Wiley & Sons, Inc.
    Additional Material: 9 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 62 (1996), S. 827-834 
    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: Polyurethanes were synthesized from polyester and butanediol with three different diisocyanates, i.e., 4,4´-diphenylmethane diisocyanate (MDI), m-xylene diisocyanate (XDI), and 2,4-toluene diiscynate (TDI). The effect of chemical structures of diisocyate compounds on the degree of crystallinity and the thermal stability were observed. Differential scanning calorimetry (DSC) and small-angle X-ray scattering (SAXS) were used to determine the degree of crystallinity of the hard segment. The thermal degradation of polyurethanes was studied by the thermogravimetric method. It has been shown that the polyurethane hard-segment crystallinity decreases in the following order: MDI〉 XDI〉 TDI〉. The experimental results also indicated that polyurethanes with aralkyl diisocyanates, i.e., XDI, had the best thermal stability. The polyurethanes synthesized from aromatic diisocyanates, i.e., MDI and TDI, had worse thermal stability than from XDI. However, owing to the higher degree of hard-segment crystallinity for polyurethanes from MDI, these polyurethanes had a better thermal stability than those based on TDI. © 1996 John Wiley & Sons, Inc.
    Additional Material: 8 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 53 (1994), S. 1165-1177 
    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 unsaturated polyesters were synthesized with various chemical structures and molecular weights. These unsaturated polyesters were used to study the curing reaction with styrene by using gel permeation chromatography and differential scanning calorimetry. The variation of the size of microgel particles during the curing reaction in unsaturated polyester-styrene resins was studied by using gel permeation chromatography. The size and structure of the microgels depend strongly on the polymer chain length and the number of vinyl groups on each unsaturated polyester chain. Using the differential scanning calorimetric method, the conversion of styrene and polyester vinyl groups during the reaction was measured. The experimental results of this study revealed that microgel formation has a great effect on the curing reaction of unsaturated polyester resins. © 1994 John Wiley & Sons, Inc.
    Additional Material: 9 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 18 (1980), S. 695-701 
    ISSN: 0360-6384
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 3 Ill.
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