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  • 1
    ISSN: 1435-1528
    Keywords: Relaxation time spectrum ; monodisperse polymer ; self-similarity ; polybutadiene melt
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Abstract The relaxation behavior of polymers with long linear flexible chains of uniform length has been investigated by means of dynamic mechanical analysis. The relaxation time spectrum (H(λ)) follows a scaling relationship with two self-similar regions, one for the entanglement and terminal zone, and a second one for the transition to the glass. This can be described in its most general form (termed “BSW spectrum”) as H(λ) = H e λne + H g λ− n g for λ 〈 λmax and H(λ) = 0 for λmax 〈 λ, where H e , H g , n e , n g are material constants and λmax is the molecular weight dependent cut-off of the self-similar behavior. In this study, the dynamic mechanical response has been measured and analyzed for four highly entangled, nearly monodisperse polybutadienes with molecular weights from 20000 to 200000. The data are well represented by the BSW spectrum with scaling exponents of n e = 0.23 and n g = 0.67. The values of the exponents obtained in this work are about the same as those found for polystyrene samples in a previous study. This suggests that the two types of polymers have a similar relaxation pattern. However, at this point further refinement of the experiments is needed before being able to draw definite conclusions about the universality of the exponents.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Rheologica acta 36 (1997), S. 330-344 
    ISSN: 1435-1528
    Keywords: Relaxation time spectrum ; monodisperse polymers ; hypergeometric function ; incomplete gamma function ; linear viscoelasticity ; polymer dynamics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Abstract The linear viscoelastic material functions of linear flexible polymers of uniform length are calculated from the BSW spectrum (Baumgaertel et al., 1990, 1992), and explicit analytic expressions are presented for several of the most common material functions for transient and dynamic experiments. However, numerical calculations are presented whenever needed. The BSW spectrum was determined from experimental G″, G″ data of two sets of molten polymers of narrow molecular weight distribution, polystyrene and polybutadiene. The purpose of the mapping is to show a wide range of viscoelastic behavior which otherwise is not available in such comprehensive form. Experimental check of these predictions is still needed in most cases. Also, some insight into the predictions for the non-linear (including the non-equilibrium) viscoelastic behavior is achieved by studying two particular experiments: the start-up of uniaxial extension at constant rate and the start-up of shear flow at constant rate.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0887-624X
    Keywords: Ziegler-Natta catalysts ; ansa-metallocene catalyst ; thermoplastic elastomeric poly(propylene) ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Racemic-anti-[ethylidene(1-η5-tetramethylcyclopentadienyl) (1-η5-indenyl)dimethyltitanium (6) has been synthesized and its molecular structure determined by x-ray diffraction methods. The two Ti=Me(1) and Ti=Me(2) units have bond distances differing by 0.08 Å and their proton NMR resonances are separated by over 1 ppm. Using this compound and methylaluminoxane (MAO) as the activator, at 25°C the 6/MAO catalyst produced polypropylene having crystalline domain with physical crosslinks. The polymers obtained at lower polymerization temperatures are rheologically liquids. The behaviors of this catalyst system resembles closely the previously reported rac-[anti-ethylidene(1-η5-tetramethylcyclopentadienyl) (1-η5-indenyl)dichlorotitanium (4)/MAO system. The structure of 6 determined here furnishes tangible support for the proposed two-state (isomeric)-switching propagation mechanism. Addition of MAO to 6 causes broadening of the Me(1) resonance in the 1H-NMR spectra, and 6 is decomposed by Ph3C+B(C6F5)-4. © 1992 John Wiley & Sons, Inc.
    Additional Material: 19 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 142 (1925), S. 257-268 
    ISSN: 0863-1786
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 8 (1985), S. 440-443 
    ISSN: 0935-6304
    Keywords: Gas chromatography ; GC/MS ; Capillary column, fused silica ; EI-MS/CI-MS ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In order to facilitate the gas chromatographic determination of butyric as well as other short chain fatty acids, triglycerides containing these fatty acids were transbutylated and transpentylated to give FABES (fatty acid butyl esters) and FAPES (fatty acid pentyl esters), respectively. This method allows the molecular weight of the compounds to be increased while their polarity is decreased. Short chain esters elute sufficiently separated from the solvent; due to the decreased polarity, elution of long chain fatty acids is only slightly retarded compared to the corresponding methyl esters. Quantitative evaluation over a large series of injections proved the linearity of correction factors in both cases, FABES and FAPES, with a slight deviation for 16:0 and 18:0, respectively. Structural characterization was performed by GC/MS. It was shown that there are characterstic fragmentations for FABES as well as for FAPES. The El-mass spectra give structural information about the alcohol and acid moieties, the ester molecule and the Cl-spectra indicate the molecular weight. The absence of abundant highly characteristic peaks in the spectra of these esters makes the detection of FABES or FAPES in complex mixtures more difficult than the detection of FAMES with their very characteristic ions at m/z 74 and 87.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 26 (1986), S. 543-553 
    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: A systematic design of the classical “coat hanger” die is proposed and tested experimentally. The objectives of the design are 1. distribution of the polymer over the width of the die before it reaches the final lip section for thickness adjustment, 2. invariance of distribution to flow rate, 3. invariance to changes in polymer viscosity, and 4. uniform average residence time. The die design is based on a flow model which assumes power-law viscosity, steady shear flow In each cross-section, uniform temperature, and separation of the flows into a manifold component and a component in a slit section of uniform height. The design corrects for an oversimplification of the pressure gradient that was applied in previous studies; and it differs from previous designs by suggesting a rectangular cross-section for the manifold. Applications to side-fed dies for extrusion blow molding and to a sheet extrusion die achieved uniform distribution and did not require any additional flow corrections (such as choker bars or flexible lips). With the new design, the lip region of the die can freely be used for thickness control, fine tuning, or further shaping of the extrudate.
    Additional Material: 16 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 27 (1987), S. 1698-1702 
    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: Dynamic mechanical measurements allow direct determination of the instant at which a network polymer gels. In such an experiment, the evolution of G′(t,ω0) and G″ (t,ω0) is measured in small amplitude oscillatory shear as a function of cross-linking time t. The frequency ω0 is kept constant throughout. At the beginning of the experiment, G″ is orders of magnitude larger than G′, and at completion of reaction, this order is reversed. It recently has been suggested by Tung and Dynes that the gel point (GP) might occur at the time at which G′ and G″ cross each other. However, there is much dispute whether GP occurs exactly at the crossover or just somewhere in its vicinity. This study resolves the dispute by modeling the rheological behavior at GP: There is only one class of network polymers for which GP coincides with the crossover. This class of polymers exhibits, when reaching GP, power law relaxation G(t) ∼ t-n with a specific exponent value n = 1/2. Examples are stoichiometrically balanced network polymers and networks with excess cross-linker, however, only at temperatures much above the glass transition. Otherwise, the power law behavior would be masked by vitrification. Power law relaxation seems to be property of polymers at GP in general. However, some polymers have a different exponent value, n ≠ 1/2, in which case the crossover occurs before GP (for n 〈 1/2) or after GP (for n 〉 1/2); i.e. the crossover cannot be used for detecting GP. While there are no networks known to us with n 〈 1/2, recent experiments showed that network polymers that are lean on cross-linker exhibit power law relaxation with n 〉 1/2. A new method is suggested for measuring GP of these imbalanced networks.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 28 (1988), S. 444-452 
    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: A numerical method has been developed for simulating fully developed multilayer shear flows of non-Newtonian fluids with arbitrary viscosity functions. Poiseuille and combined Poiseuille/Couette flows in both slits arid annuli may be modeled. The method employs a finite difference system where grid points lie on streamlines and move to their correct positions as the solution procedure converges. Interfaces are easily handled as particular stream lines with the equation of motion replaced by a boundary condition. The method is stable for high interface viscosity ratios and readily handles a large number of layers. Many authors have employed power law models to model multi-layer non-Newtonian flows. We find that the power law is sufficient to predict pressure gradients and interface positions in most cases, but gives unrealistically flat velocity profiles, even when truncated at finite viscosity. Results are presented for the Carreau fluid and for the rubber-like liquid with shear thinning via Wagner's strain functional.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 45 (1992), S. 451-459 
    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: Reaction of methylenedianiline and maleic anhydride in acetone, followed by cyclodehydration in the presence of acetic anhydride and 1,4-diazabicyclo [2.2.2] octane as a catalyst, affords a mixture of compounds, Desbimid, with maleimide, isomaleimide, and acetamide groups. Dissolution of this mixture in styrene and 2-hydroxyethyl methacrylate results in clear liquid resins. The viscosity of the formulated resins ranges from 100-1700 mPas at 25°C depending on the concentration of Desbimid. These systems can be processed and cured at ambient temperatures until demoulding and postcured at temperatures up to 200 or 250°C. The flexural modulus, flexural strength, and elongation at break of a number of cured formulations are found between 3500-3800 N/mm2, 90-115 N/mm2, and 2.7-3.5%, respectively.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 27 (1987), S. 1390-1398 
    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: A numerical method is described for calculating the stress a viscoelastic melt exhibits in a flow, based on approximate kinematics. The method assumes that the kinematics are reasonably close to those of a shear-thinning fluid such as the Carreau model. The strain history of a given flow and the resulting stress are calculated via a tracking method from finite element kinematics. Fullfield flow birefringence experiments were done for lowdensity polyethylene and polystyrene flowing past a thin plate divider in a 1.254-mm planar slit die. By digitally analyzing birefringence photographs of the flow field, the birefringence was measured over two dimensions. These birefringence results are in good agreement with birefringence fields calculated from the numerical simulations and the stress-optical law. The flow fields were most highly oriented in a region surrounding the weld interface just downstream of the plate divider. This orientation relaxed farther downstream, with polystyrene relaxing faster than low-density polyethylene.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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