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  • Articles: DFG German National Licenses  (10)
  • 1990-1994  (10)
  • 1965-1969
  • 1915-1919
  • 1993  (10)
  • Chemistry  (10)
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  • Articles: DFG German National Licenses  (10)
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Years
  • 1990-1994  (10)
  • 1965-1969
  • 1915-1919
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  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 31 (1993), S. 129-134 
    ISSN: 0887-624X
    Keywords: ionomers ; telechelic polymers ; quaternary ammonium sulfonate ; thermal stability ; degradation ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The thermal stability of telechelic polystyrenes bearing quaternary ammonium iodide or ammonium sulfonate end groups is presented. It appears that the ammonium iodide functions are stable below 200°C. Above that temperature, the polystyrene irreversibly looses its functional end groups. The weight loss then observed leads to the conclusion that a Hofmann-type degradation mechanism is likely to take place. In contrast, the ammonium sulfonate-terminated polystyrene begins to degrade at 180°C and leads to a polymer which is no longer end-capped with sulfonic acid or sulfonate groups. This behavior is of importance, especially for the study of multiblock ionic copolymers which are prepared by blending two telechelic polymers, one of them bearing sulfonic acid end groups and the other one tertiary amine functional groups. © 1993 John Wiley & Sons, Inc.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 39 (1993), S. 745-756 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: The flow field inside an orifice flowmeter with a beta ratio of 0.50 operating at a Reynolds number of 91,100 has been studied using a three-color, 3-D laser Doppler anemometer system. Mean velocity measurements show large radial velocities leading into the orifice, the fluid separating from the orifice plate at the throat, the presence of a vena contracta farther downstream, flow reattachment to the pipe wall 5.3 pipe radii (R) downstream, the presence of a small upstream recirculation zone, and both a primary and secondary recirculation zone downstream of the orifice plate. The static wall pressure distribution attains a minimum pressure at 1.5 R, which does not coincide with the location of the vena contracta (0.75 R). Distributions of the entire Reynolds stress tensor are presented along with calculated values of turbulence kinetic energy, turbulence kinetic energy production, vorticity, and turbulence induced accelerations. These data are analyzed to interpret the complex turbulent flow field.
    Additional Material: 16 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 31 (1993), S. 719-727 
    ISSN: 0887-6266
    Keywords: phase separation of crystalline and miscible polymer blends ; blends of poly(ε-caprolactone) and poly(styrene-co-acrylonitrile) phase separation of ; differential scanning calorimetry (DSC) of blends of poly(ε-caprolactone) and poly(styrene-co-acrylonitrile) ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The phase separation of a crystalline and miscible polymer blend, poly(ε-caprolactone) /poly(styrene-co-acrylonitrile) (PCL/SAN), has been studied by differential scanning calorimetry (DSC), using a SAN containing 28.3% of acrylonitrile units. Several phenomena can be associated with the occurrence of phase separation depending upon the composition of the mixture. Following annealing at high temperatures, below and above the phase separation temperature Tc, three cases can be distinguished. In Case I, there is no sign of crystallization during quenching and DSC scanning, but a melting peak is observed at Tc, and above. In Case II, there is no crystallization on quenching but it does occur during the DSC run; the shift of the crystallization peak can then be related to Tc. In Case III, there is crystallization on quenching, and additional crystallization during the DSC run; the change of area of the crystallization peak is indicative of Tc. From these observations, the phase diagram of the system was determined. © 1993 John Wiley & Sons, Inc.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 31 (1993), S. 255-264 
    ISSN: 0887-6266
    Keywords: polyethylene, UHMW, crystal orientation in drawn films of ; x-ray diffraction study of crystal orientation in drawn films of UHMW polyethylene ; crystal orientation of UHMW polyethylene in drawn films ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A wide-angle x-ray diffraction (WAXD) study of the development of molecular orientation in the crystalline phase of ultra-high-molecular weight polyethylene films prepared by the gelation-crystallization method is presented. WAXD scans of the undrawn films show that the lamellae are oriented in the plane of the films. Upon drawing at 130°C, the orientation of the molecular chains changes from the direction normal to the film surface (ND) to the elongation direction. The decrease of the 200/020 intensity ratio at low draw ration (λ 〈10) indicates that double orientation develops during the transformation from the lamellar to the fibrillar morphology, with the a-axis oriented parallel to ND. The orientation distributions of the 110, 200, 020, and 002 planes of the orthorhombic unit cell of polyethylene were studied and characterized by the coefficients of a Legendre polynomial series. At a draw ratio of 4.5, the second-order coefficient, 〈P2(cos χ〉, already gets close to its limiting value, but it is shown that higher order coefficients of the polynomial series can be used to describe the evolution of the orentation, even up to λ = 50. The coefficients relative to the molecular chain orientation, 〈Pn(cos χ)〉c, can be calculated from different crystalline reflections. Curve-fitting calculations were made in order to improve the correlation between the results obtained from the orientation distribution of the 110, 020, and 002 planes. A Person VII function was found to give a better fit of the experimental curves than Gaussian or Lorentzian equations. © 1993 John Wiley & Sons, Inc.
    Additional Material: 8 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 47 (1993), S. 1621-1631 
    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 dense films and membranes was prepared using different processes; their surface morphology was investigated by transmission electron microscopy using the replication technique. On the basis of TEM results, SEM observations of cross sections of membranes and gas-separation properties of membranes, two kinds of membrane morphology are evidenced in relation to their preparation conditions and final properties. The first one gives an ultrafiltration-type membrane. Large nodules are observed on the surface of the membranes. It is suggested that these are formed by liquid-liquid separation that occurs by nucleation and growth of the polymer-rich phase. The second one yields gas-separation-type membranes. No nodules are evident at the surface of these membranes. The skin is formed by a step that concentrates the initial solution. It is followed by the transformation of the solution in the glassy state. Liquid - liquid separation takes place below the first skin layers by nucleation and growth of the polymer-poor phase. © 1993 John Wiley & Sons, Inc.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 48 (1993), S. 85-97 
    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: Normally brittle polystyrene (PS) can be toughened effectively by the inclusion of a few weight percent of low molecular weight polybutadiene (PB). The PB, which can be made to phase separate into submicron sized, randomly dispersed pools, locally plasticizes the glassy phase in the vicinity of a growing craze; the resulting reduction in craze flow stress and increased craze velocity lead to significant enhancement of toughness when strain rates are below approximately 10-1 s-1. Craze velocities were measured in PS containing 1 to 5 wt % of a low molecular weight PB (2300 g/mol). The results were compared to a version of the interface convolution mechanism for craze growth that has been modified to account for the localized plasticization effect of the low molecular weight diluent. Addition of 5 wt % PB led to craze velocities that are three orders of magnitude larger than observed for pure PS. The model deviated significantly from the experimental data at the higher and of the PB concentration range studied here, but it did exhibit the general form of the observed dependence of craze velocity on PB content. © 1993 John Wiley & Sons, Inc.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 27 (1993), S. 207-216 
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: We have partially characterized surface glycoproteins of the canine heartworm, Dirofilaria immitis. Histochemical studies indicated the presence of neutral and acidic mucopolysaccharides at the blood-cuticle interface. Fluorescein isothiocyanate-conjugated lectin binding patterns suggested the presence of α-D-glucosyl and/ or α-D-mannosyl, β-galactosyl, N-acetylneuraminyl and N-acetylated-D-hexosaminyl (sialic and glucuronic acids, respectively) terminal residues among the constituent sugars of the glycocalyx. An additional goal of this study was to assess the significance of each carbohydrate in parasite hemocompatibility by using scanning electron microscopy, internal reflection infrared spectroscopy, and comprehensive contact angle measurements. Each carbohydrate identified in the glycocalyx was selectively cleaved with the appropriate exoglycosidase. Heartworms bearing native and enzyme-altered surfaces were exposed to platelet-rich canine plasma. Activation and aggregation of platelets were significantly increased on enzyme-treated surfaces as compared with native surfaces. Enzyme-induced cleavage of carbohydrate residues was associated with an increase in critical surface tension or a loss in cuticular structural integrity or both. Hemocompatibility of the heartworm cuticle depends on the retention of a stable saccharide-rich layer that minimizes interaction with plasma proteins and platelets; thus, carbohydrate residues on the glycocalyx may contribute to parasite hemocompatibility. The presence of similar low-critical-surface-tension coatings with high mechanical integrity may impart thromboresistance to other polyphenolic or chitinous substances. © 1993 John Wiley & Sons, Inc.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 0570-0833
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 25 (1993), S. 199-203 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Rate constants have been measured in aqueous solutions for the reactions of the carbonate radical, CO3·-, with several saturated alcohols and one cyclic ether as a function of temperature. Arrhenius pre-exponential factors ranged from 2×108 to 1×109 l mol-1 s-1 and activation energies ranged from 16 to 29 kJ mol-1. The results suggest that the reactions are not pure hydrogen abstraction, but involve an additional interaction of the radical with the —OH or —O— linkage. © 1993 John Wiley & Sons, Inc.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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