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  • 1
    ISSN: 1435-1528
    Keywords: Rheology ; liquid crystal ; monodomain ; instability ; conoscopy ; shear
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Abstract We have measured the shear-induced rotation of the nematic director in a liquid crystalline polymer using poly benzyl glutamate (PBG) as model system. PBG is a well characterized synthetic poly (α amino acid) with rigid chain architecture and well defined conformations. For the experiments it is important to start out with a sample in which the molecules are highly aligned with a uniform director. This so-called monodomain morphology is obtained by use of strong magnetic fields and surface modifications of the sample holders. When shearing the monodomain at a constant rate, the macromolecules rotate initially homogeneously until a periodic director pattern develops. These spatially periodic structures emerge in a narrow range of shear strain and, as shearing continues, disintegrate into a chaotic texture. By varying the initial monodomain director with respect to the flow direction (but within the shear planes) we could show that the periodic patterns do not depend on the shear direction; they are governed by the director of the initial monodomain. We observe conoscopically that at high shear rates the texture becomes uniformly aligned. The molecules are aligned preferentially with an angle of about 4° to the shear direction (against vorticity direction). Interestingly, this agrees very well with predictions made by Larson (1990).
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Rheologica acta 35 (1996), S. 645-655 
    ISSN: 1435-1528
    Keywords: Rheology ; polymers ; poly-dispersity ; linear viscoelasticity ; relaxation time
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Abstract The relaxation of slightly poly-disperse linear flexible polymers has been expressed in a simplified blending rule which is presumed to be a weighted linear superposition of the relaxation spectra of mono-disperse components which constitute the blend. Discrete components are characterized by their molecular weight M i,weight fraction w i,and relaxation time spectrum H i(λ). ). In contrast to broadly distributed blends in which the small molecules mobilize the large ones and vice versa, we introduce the term “slightly polydisperse” for blends with molecular weight distributions narrow enough to have very little change in the longest relaxation times of each molecular weight component. The properties of this blending rule are analyzed and dynamic data is calculated for slightly poly-disperse polystyrene. As an application, the blending rule is used to determine the characteristic mono-disperse parameters (BSW parameters) of two materials, poly (vinyl methyl ether) and polycarbonate, for which we could not determine their BSW parameters directly since they were not available in nearly monodisperse form. The proposed blending rule can only be applied to systems in which all components are above the entanglement molecular weight, i.e. M i≫M c.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0009-286X
    Keywords: Chemistry ; Industrial Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 30 (1990), S. 408-415 
    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 that takes the streamline finite difference method for modeling fully developed multilayer polymer flows and adds to it a simple means of accounting for nonisothermal conditions. In industrial practice, temperature control is often used to match material viscosities and, thereby, to avoid flow instabilities. By numerically calculating both viscosity ratios and normal stress difference ratios, the numerical method allows one to judge the relative stability of different flows and to choose an intelligent set of experiments when designing a coextrusion process. The algorithm has been successfully tested for a number of polymer melt constitutive equations in flows where the viscosity jumps no more than two orders of magnitude between fluids. Results for a rheologically well characterized polystyrene low-density polyethylene system and for an industrially interesting high-density polyethylene/Ultem system show that the common practice of matching zero-shear viscosities is overly simplistic when interface shear rate, conduction, normal stress, and flow rate effects are taken into account.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 33 (1987), S. 1585-1600 
    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: Linear viscoelastic properties are found to be a sensitive measure of flow-induced structural changes in a block copolymer. Styrene-butadiene-styrene block copolymer (SBS) with 26% polystyrene (PS) forms a macrostructure in the quiescent state with grains of the order of 1-10 μm. Within each grain, phase separation gives rise to a regular two-phase microstructure with cylindrical PS domains with radius of the order of 200 Å. Large-amplitude oscillatory shear (γ = 4.5) at temperatures between 139 and 181°C was applied to after the grain structure with the objectives of removing the discontinuities at the grain boundaries and of aligning the domains into a continuous ultrastructure. The SBS behaved like a solid (tan δ 〈 1 at low ω) before and like a liquid (tan δ 〉 1) after shear modification. This change expressed itself in the removal of the long relaxation times from the linear viscoelastic spectrum; the intermediate and low relaxation times were not affected by the shear modification. The viscoelastic spectrum slowly recovered during annealing with recovery times of the order of the longest relaxation time of the quiescent structure. Birefringence studies showed that the SBS did not recover into its original grain structure but into a highly oriented domain structure. The discontinuities at the grain boundaries could not be removed completely.
    Additional Material: 14 Ill.
    Type of Medium: Electronic Resource
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  • 6
    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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  • 7
    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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  • 8
    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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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 72 (1960), S. 522-522 
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 48 (1935), S. 610-614 
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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