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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 235 (1996), S. 35-45 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Ein Phenolharz-Polyurethan-Copolymeres wurde aus einem Phenolharz, einem geschützten Polyurethan und p-Toluolsulfonsäure hergestellt. Dieses Copolymere weist trotz großer Härte eine gute Verarbeitbarkeit (einschließlich Topfzeit und Reaktivität) auf. Die Synthese des Copolymeren wurde mit IR-Spektroskopie verfolgt. Es wurde gefunden, daß die Isocyanatgruppe des Polyurethans nach Abspaltung der Schutzgruppe mit der Hydroxygruppe des Phenolharzes reagierte. Glasfaserverstärkte Verbundwerkstoffe offenbarten bei SEM-Untersuchungen eine hervorragende Verbindung zwischen Faser und Matrix. Ein Überlappungspeak im DMA-Diagram wies auf Wechselwirkungen zwischen Phenolharz und Polyurethan hin, die die Härte des Phenolharzes verbessern.
    Notes: A phenolic resin/polyurethane copolymer was synthesized by reaction of a phenolic resin, a blocked-polyurethane and p-toluene sulfonic acid. The copolymer provides a good balance between the processability (including pot life, reactivity) and toughness. The reactions that proceeded during the synthesis of the copolymer was investigated by IR spectroscopy. It was found that blocked polyurethane reacted with the hydroxy group of the phenolic resin. Glass fiber-reinforced composites showed excellent bonding between fiber and matrix as revealed by SEM photographs. An overlap peak was found from the DMA diagram; it indicated that an interaction existed between phenolic resin and polyurethane and that improved the toughness of the phenolic resin.
    Additional Material: 7 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Computational Chemistry 19 (1998), S. 1555-1566 
    ISSN: 0192-8651
    Keywords: molecular dynamics simulation ; semiflexible models ; macromolecules ; constraint dynamics ; helix folding ; Chemistry ; Theoretical, Physical and Computational Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Computer Science
    Notes: Semiflexible models are often used to study macromolecules containing stable structural elements. Based on rigid body dynamics, we developed a rigid fragment constraint dynamics algorithm for the simulation of semiflexible macromolecules. Stable structural elements are treated as rigid fragments. Rigid fragment constraints, defined as combinations of distance constraints and position constraints, are introduced to limit internal molecular motion to the required mode. The constraint forces are solved separately for each rigid fragment constraint and iteratively until all constraint conditions are satisfied within a given tolerance at each time step, as is done for the bond length constraint in the SHAKE algorithm. The orientation of a rigid fragment is represented by the quaternion parameters, and both translation and rotation are solved by the leap-frog formulation. We tested the algorithm with molecular dynamics simulations of a series of peptides and a small protein. The computation cost for the constraints is roughly proportional to the size of the molecule. In the microcanonical ensemble simulation of polyvalines, the total energy was conserved satisfactorily with time steps as large as 20 fs. A helix folding simulation of a synthetic peptide was carried out to show the efficiency of the algorithm in a conformational search.   © 1998 John Wiley & Sons, Inc.   J Comput Chem 19: 1555-1566, 1998
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  • 3
    Electronic Resource
    Electronic Resource
    Brookfield, Conn. : Wiley-Blackwell
    Polymer Composites 16 (1995), S. 215-223 
    ISSN: 0272-8397
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Fatigue behavior of carbon fiber reinforced poly(etheretherketone)(PEEK) laminates was investigated. The static tensile measurement, tension-tension fatigue loading tests, and residual tensile strength measurement of the [0/45/90/-45]2s AS-4/PEEK laminates were performed at various levels of stress amplitudes. The influences of stress amplitude on the fatigue life and the residual tensile strength were investigated. The experimental results for fatigue life and residual tensile strength under different stress amplitudes are analyzed by the median rank method. The S-N curves at various survival probabilities are also presented by the pooled Weibull distribution function. Furthermore, a residual strength degradation model is used to predict the residual strength for the composites subjected to a number of fatigue cycles and to simulate the effects of the stress amplitude on the fatigue life. The agreement between experiment and theory is good.
    Additional Material: 17 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Electrophoresis 16 (1995), S. 1474-1478 
    ISSN: 0173-0835
    Keywords: Capillary isoelectric focusing ; Imaging detection ; Laser induced fluorescence ; Proteins ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: A simple laser-induced fluorescence (LIF) imaging detector and an ultrasensitive LIF imaging detector are described for capillary isoelectric focusing (CIEF). An argon ion laser beam of 496.5 nm is used as excitation source. In the simple LIF imaging detector, the excitation beam is directed into a capillary column by an optic fiber array. In the ultrasensitive LIF imaging detector, the laser beam is first expanded, then is focused into the 4.5 cm long capillary column by a cylindrical lens. Fluorescence emission is detected by a charge-coupled device (CCD) camera. The feasibility and performance of the LIF imaging detector system for CIEF are first verified with a naturally fluorescent protein, b-phycoerythrin. Then, the ultrasensitive LIF imaging system is used as a detector for CIEF of proteins labeled with fluorescein isothiocyanate (FITC). Three FITC-labeled proteins (i) α-D-galatosylated FITC-albumin, (ii) insulin-FITC, and (iii) casein-FITC, are used as model samples. Fluorescence images of the model samples are measured during the CIEF process. The focusing of the protein samples is complete in about 1.5 min. The ultrasensitive detector's detection limits for the FITC-labeled proteins are at the level of 10-10 M, and the mass detection limits are about 4.5 × 10-17 mole, even though only 10% of the fluorescence emission is collected. Therefore, the method is capable of separating and detecting 10-11 M or amole (10-18 mole) level protein samples with a band-pass filter more specific to the fluorescence light. Potential applications of the LIF imaging system in addition to quantitation of separated fluorescent species in various capillary electrophoresis methods can also include investigation of interaction between analytes focused in a capillary column.
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  • 5
    ISSN: 0323-7648
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: X-ray methods have been used to investigate the structure of fibers of aromatic copolyimides prepared from 3,3′,4,4′-biphenyltetracarboxylic dianhydride (BPDA), o-tolidine (OTOL) and p-phenylene diamine (PPD). We have shown previously that the non-periodic layer lines in the X-ray fiber diagrams of these copolymers are indicative of a random comonomer sequence. In the present paper, we analyze the shifts in the layer line positions that occur with increasing draw ratio. These changes are to be understood primarily in terms of increases in the correlation lengths for the stiff chain conformation. At high draw ratios there is also evidence for the development of a more extended chain conformation, probably due to torsional variation changes in the torsion angles. It is shown that the data are sufficiently sensitive to allow quantitative analysis of these separate effects, and their dependence on comonomer ratio.
    Additional Material: 9 Ill.
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  • 6
    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: In this paper the swelling and melting behavior of several polymers, particularly acrylic fibers, is studied by thermomicroscopy and differential scanning calorimetry in detail. It is confirmed that the protrusion peak on the tail part of the DSC thermogram of swelling polymers is closely associated with the macromolecular entanglements. The proposed swelling DSC method is proved to be very effective for studying polymer entanglements. It is also shown that the melting point, whether of paracrystalline region or of entanglement structural unit, can be well fitted to Flory's melting point depression theory.
    Additional Material: 3 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 45 (1992), S. 871-886 
    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 texture of a polymer (on fiber) is effectively developed by heat and stress. In this article, the chief material studied is acrylics, usually polyacrylonitile copolymer (PAC fiber) produced by Jingshan Jinglun Fiber Production Plant. In industry, the Jinglun acrylic fiber is heat treated, using saturated steam, at a temperature of 120-130°C to enhance its loop strength, reduce shrinkage, and stabilize crimp. At 140°C, the fiber becomes tacky and its good textile properties seem to deteriorate. At 150-160°C, the texture of the fiber seems to be deeply modified. Tested by differential scanning calorimetry (DSC) with the fiber immersed in a swelling agent (usually termed swelling DSC, abbreviated as SDSC), in addition to the entanglement peaks situated on the latter part of the thermogram of the Jinglun fiber, a new endothermic peak before the crystalline peak (actually, paracrystalline in the case of acrylic fiber) was discovered. The elastic recovery properties of the treated fiber under partially swelling conditions were improved. This seems to indicate that this preparacrystalline peak might also be concerned with entanglements.
    Additional Material: 18 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 42 (1991), S. 1779-1791 
    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 relationships among internal stress, lattice deformation, and the moduli of polymers, such as poly(ethylene terephthalate) (PET), polypropylene (PP), polyethylene (PE), polyacryonitrile (PAN), and poly(p-phenylene terephthalamide) (PPTA), have been studied systematically. Compared to small molecule crystals, polymer crystals have many more defects and their parameters of the crystal unit cells and the density of the crystalline region are easy to vary to a certain extent. During the processing, external stresses were put on the polymer fibers and polymer molecules were drastically deformed, which induced polymer crystallization and preferred orientation. After processing, there are many macromolecules frozen in the nonequilibrium status, which is the cause of internal stress. Heat treatment could give energy to the macromolecules to release the internal stress and to approach thermodynamic equilibrium. For polymer crystals, the higher the annealing temperature, the shorter the lengths of the unit cell axes, the more integral and regular the crystal lattice, and the smaller the unit cell volume. Crystalline modulus changes not only with different kinds of polymer materials, but also with measurement temperature and processing history. Polymer processing, mainly drawing, causes orientation and internal stress which causes lattice deformation and raises tensile modulus of polymer materials.
    Additional Material: 7 Ill.
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  • 9
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The fast atom bombardment (FAB) mass spectra and low-energy collisional activation mass spectra of ions generated under FAB were investigated for twelve bisbenzylisoquinoline (BBI) alkaloids. The relative molecular mass of the free base and diquaternary BBI alkaloids can be obtained from FAB data. However, monoquaternary ammonium salts produce only an [M  -  X]+ ion and the relative molecular mass cannot be determined. For Type A (single ether linkage) BBI alkaloids, fragmentation occurs primarily from benzylic and ether cleavages. Thus, the total number of aromatic substituents (OH, OCH3 or OCH2O) can be determined for rings A-B, C-D, E and F. For Type B (two either linkages) BBI alkaloids, fragmentation occurs primarily from double benzylic cleavages. Hence only the total number of aromatic substituents can be determined for the upper half of the Type B BBI alkaloids, i.e. rings A-B and C-D. An unknown alkaloid was examined to illustrate the utility of the fragmentation schemes.
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  • 10
    ISSN: 0894-3230
    Keywords: cryptand ; fluorescence titration ; lanthanide coordination ; proton transfer ; Chemistry ; Theoretical, Physical and Computational Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Lanthanide [lanthanum(III), 2; europium(III), 3; and gadolinium(III), 4] cryptates of a tris-phenylphenol N8O3 Schiff-base cryptand (H3L) were synthesized by transmetallation with [Na(H3L)]ClO4·3H2O (1) and characterized by spectroscopic and crystal structure analyses. Both 3 and 4 are isomophous and isostructural. The complexes crystallize in the triclinic space group P-1 with cell parameters for 3 of a = 14.9833(2), b = 15.42670(10), c = 16.3770(3) Å, α = 75.3760(10), β = 68.2640(10), γ = 77.0540(10)° and Z = 2 and for 4 of a = 14.9976(3), b = 15.4417(3), c = 16.35350(10) Å, α = 75.4980(10), β = 68.3180(10), γ = 76.8790(10)° and Z = 2. The structures reveal that one lanthanide ion is unsymmetrically encapsulated in the cryptand cavity with a second ligand (solvent DMF). Solution NMR and solid structural studies demonstrated that there are intracavity and intermolecular proton transfer processes during lanthanide complexation towards the cryptand. A fluorimetric titration in acetonitrile for Eu(III) ion to 1 afforded a novel fluorescence intensity (IF)-equivalents of Eu(III) ion (x) plot signaling a quenching (0 〈 x 〈 0.2)-enhancement (0.2 〈 x 〈 1) change with formation of the kinetically stable 1:1 cryptate. An energy-transfer mechanism is discussed. Copyright © 1998 John Wiley & Sons, Ltd.
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