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  • GEOPHYSICS  (163)
  • Polymer and Materials Science  (67)
  • Lunar and Planetary Science and Exploration  (64)
  • EARTH RESOURCES AND REMOTE SENSING  (32)
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  • 11
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 15 (1971), S. 811-828 
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: An attempt has been made to rationalize the variables in the preparation procedure of Loeb-Sourirajan-type reverse-osmosis membranes. The quaternary phase diagram of the system cellulose acetate-acetone-formamide-water was determined and has proved a useful tool in the discussion of membrane structures and properties. A mechanism based on differences in the precipitation rate of the polymer during the membrane formation process has been suggested to explain the observed asymmetry in the membrane structure. The porosity of the membrane has been ascribed to the relative rates of water entering and solvent leaving the cast film. The effects of the casting solution composition, the evaporation time, the wash bath temperature, and the annealing procedure have been studied. X-Ray diffraction and electron microscopy were used to supplement flux and retention data of membranes made from a cellulose acetate-formamide-acetone casting solution.
    Zusätzliches Material: 14 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 12
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 14 (1970), S. 1197-1214 
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Batch and flow recirculation cells were used to study the properties of high-flux ultrafiltration membranes with different macromolecular solutions. At low pressures, solutions of completely retained macromolecular solutes have a flux which is approximately the same as the flux of pure solvent. At higher pressures, the solution flux levels off. The flux, at the leveling-off period, is approximately inversely proportional to the solution concentration. In this plateau region the flux increases with temperature and agitation of the solution but decreases with time. These results are explained by the formation of a gel layer on the membrane surface during the filtration of macromolecular solutions. In ultrafiltration, in contrast to dialysis and GPC, a linear polymer penetrates the selective barrier more readily than does a globular protein of the same molecular weight. The difference may arise from the liquid shear stresses within the barrier medium due to the movement of fluid relative to the pore walls, which is large only in ultrafiltration. Also, retention of polymers was found to decrease with pressure and to increase with agitation of the solution.
    Zusätzliches Material: 13 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 13
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: A black charcoal-like material having cation exchange and adsorption properties was prepared by the controlled pyrolysis of starch in the presence of a commercial phytic acid solution. Resins with binding capacities of 0.7-5.7 meq/g of calcium were prepared by varying the phytic acid to starch ratio, the temperature, or the duration of heating of the reaction mixture. SEM photomicrographs of some of these new materials showed that they are composed of particles similar in size and shape to the starting starch granules. These resins also removed atrazine from aqueous solutions. © 1995 John Wiley & Sons, Inc.This article is a US Government work and , as such, is in the public domain in the United States of America.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 14
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 39 (1990), S. 655-678 
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Polystyrene (PS) and polyethylene (PE), along with their reactive counterparts, i.e., polystyrene having oxazoline reactive groups (OPS) and polyethylene with carboxylic acid groups (CPE), were melt blended in a Rheomix mixer. These blends were prepared by mixing these polymers in various proportions under a variety of conditions. In an alternate procedure the OPS, CPE graft polymer (OPS-g-CPE) was prepared by melt blending these two polymers beforehand, and subsequently this grafted polymer was used as a compatibilizer for PS-PE blends. The effects of the addition of OPS and CPE, on the one hand, and OPS-g-CPE, on the other hand, on the compatibility of PS-PE blends were investigated. The morphology of these blends was examined with a scanning electron microscope (SEM) and related to their tensile properties. The PS-PE blends are found to have the typical coarse morphology of incompatible blends and poor tensile properties while their reactive counterparts, OPS-CPE blends, have fine grain microstructure and show improved tensile strength throughout the range and improved elongation in the PE-rich blends. Relatively low concentrations of the reactive pair, oxazoline and carboxylic acid, are shown to be necessary to produce improved compatibility. The preblended graft copolymer OPS-g-CPE imparts compatibility to PS-PE blends also but not as effectively. This suggests that the addition of OPS and CPE during melt mixing of PS and PE forms OPS-g-CPE polymer at the interface and that these ingredients act as “in situ reactive compatibilizers” which improve physical properties.
    Zusätzliches Material: 10 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 15
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 41 (1990), S. 1299-1313 
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Functionalization of molten linear low-density polyethylene (LLDPE) with 2-(dimethylamino)ethyl methacrylate (DMAEMA) was studied in an intermeshing co-rotating twin-screw extruder using a peroxide initiator. The influence of monomer concentration, initiator concentration, reaction temperature, the screw speed, and the mean reaction residence time on the grafting reaction was investigated in order to determine the reaction conditions necessary to obtain a controlled degree of grafting, DG, while minimizing homopolymerization and crosslinking. Relatively high grafting levels can be obtained without excessive polyethylene crosslinking by using high monomer concentrations, wm, with low initiator concentrations, wI. DG increased with increasing monomer concentration when wm exceeded a certain value. Processing temperatures between 130 and 160°C are optimal to achieve high grafting efficiency, GE. Too high a processing temperature resulted in both low DG and GE. An optimal reaction residence time of about 5 min was found for wm = 23 wt % and wI = 0.56 wt % to obtain relatively high DG and GE. The melt flow index of the reaction product, MFI, increased with increasing wm at constant wI. This suggests that the DMAEMA monomer has the ability to suppress crosslinking of the LLDPE chains. The ability of the DMAEMA monomer to compete for initiator and polymer radicals and reduce LLDPE crosslinking was further demonstrated by the study of sequential addition of monomer and initiator along the extruder. The competition among the three reactions (i.e., the desired grafting, homopolymerization, and crosslinking) is discussed.
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 16
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 48 (1993), S. 1199-1208 
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Using organic peroxide initiators in the melt grafting of monomers containing amino groups onto polyethylenes is known to cause serious discoloration of the resulting polymers. To eliminate the discoloration while preserving the controlled degree of grafting, a nonoxidative and hydrogen-abstracting initiator with appropriate thermal stability is needed. In this study, the hydrogen-abstracting capability of three azo initiators with suitable decomposition rates in the melt grafting temperature ranges was evaluated using polyethylene cross-linking and polypropylene degradation experiments (called “hydrogen-abstracting experiments”). Among the three azo initiators tested, only a phenylazo initiator, 2 - phenylazo - 2,4 - dimethyl - 4 - methoxyl - valeronitrile (V-19), demonstrated strong hydrogen-abstracting capability from polymer backbones. These three azo initiators were used in the melt grafting of 2 - (N, N - dimethylamino) ethyl methacrylate (DMAEMA) and 2-(N-t -butylamino) ethyl methacrylate (tBAEMA) onto a linear low-density polyethylene (LLDPE). In agreement with the results obtained from the hydrogen-abstraction experiments, only V-19 led to a considerable amount of grafting of both DMAEMA and tBAEMA onto LLDPE. As expected, polymers grafted with V-19 showed significantly reduced discoloration compared with those grafted with peroxide initiators. Further examination of the grafting results indicated that the initiator efficieny, defined as the number of grafted monomer units per radical generated from initiator decomposition, was higher with the phenylazo initiator than with peroxide initiators. The hydrogen-abstracting capability of the phenyl free radical generated from the decomposition of V-19 was estimated to be higher than peroxide and methyl free radicals produced in the decomposition of peroxide initiatros. © 1993 John Wiley & Sons, Inc.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 17
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 62 (1996), S. 1807-1818 
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Very few polymeric systems are suitable for preparing engineering parts using reaction injection molding (RIM) processing. A new two-component metallocene catalyst, which is able to polymerize bulk styrene at high rates to the syndiotactic form, was studied. The catalyst used in this work was based on monocyclopentadienyl analogs of titanium (Cp*TiMe3), which was used in conjunction with a boron cocatalyst [B(C6F5)3]. When separate streams of the catalyst and cocatalyst, dissolved in either styrone or styrene/toluene solutions, met in a mixhead, the styrene polymerized rapidly to form crystalline, syndiotactic polystyrene (s-PS). Using a bench scale RIM device, the monomer conversion during polymerization was monitored through the quasi-adiabatic temperature rise, recorded by a rapid data acquisition system. The rate equation was found to be second order with respect to the monomer concentration and first order with respect to the catalyst concentration, given some assumptions. The s-PS was brittle and attempts were made to incorporate elastomer toughening into the reacting system. Several potential problems associated with using this system for RIM process discussed. © 1996 John Wiley & Sons, Inc.
    Zusätzliches Material: 10 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 18
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 15 (1971), S. 411-417 
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: A simple method is presented for correction of polydispersity obtained by gel permeation chromatography. The method proposed utilizes well-characterized polystyrene standards for both instrument calibration and construction of a correction curve which is then used for calculation of weight-average and number-average molecular weights and polydispersity of samples to be characterized.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 19
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 21 (1977), S. 2375-2392 
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: The techniques of Auger electron spectroscopy (AES) and x-ray photoelectron spectroscopy (XPS) have been used to study the locus of failure of epoxy resin joints. The effects of a long water immersion and the application of a silane-based primer have also been studied. Results indicated that for dry joints fracture occurred near an epoxy resin/metal interface while with water-soaked unprimed joints, fracture occurred interfacially between the adhesive and iron oxide. The application of the primer to the metal surface prior to bonding prevented the formation of a water-formed oxide although fracture was then found to occur through the primer.
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 20
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 22 (1978), S. 1991-2009 
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: The kinetics of drug release from a series of partial esters of vinyl acetate-maleic anhydride has been investigated. These polymers in their un-ionized forms are hydrophobic and water insoluble, but in their ionized forms they are water soluble. Polymer dissolution is pH sensitive, and different half-esters have a characteristic pH range above which they are soluble and below which they are insoluble. When films are placed in buffered media, they erode at a constant rate that depends on the pH of dissolution of the polymer and on the pH of the buffered medium. Dissolution of the polymer is limited to the polymer-buffer medium interface, and drugs dissolved or uniformly dispersed in the polymer are released by zero-order kinetics. A detailed model has been developed that successfully correlates dissolution behavior and various experimental parameters.
    Zusätzliches Material: 16 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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