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  • Polymer and Materials Science  (229)
  • 1990-1994  (229)
  • 1991  (229)
  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 42 (1991), S. 225-232 
    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 micelle-forming monomers of sodium 6-acrylamidocaproate (Na 6-AAC), sodium 11-acrylamidoundecanoate (Na 11-AAU), sodium 11-(N-methylacrylamido) undecanoate (Na 11-MAAU), and sodium 11-(N-ethylacrylamido) undecanoate (Na 11-EAAU) have been synthesized and polymerized. Except poly(Na 6-AAC), the molecular weights of the other three poly(sodium acrylamidoalkanoate) s were over 106. They behave as strong anionic polyelectrolytes in aqueous solutions. Their solution properties, such as viscosity, charge density, and radius of gyration, were investigated. The performance of these anionic polyelectrolytes as coagulant aids in water treatment were assessed by jar test. Poly(Na 6-AAC) and poly (Na 11-AAU) were superior to poly (Na 11-MAAU) and poly (Na 11-EAAU) in terms of flocs settling. All these four anionic polyelectrolytes tested in water treatment are as effective as a commercially available cationic polyamine organic coagulant (Hyperfloc CP 753).
    Additional Material: 6 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim [u.a.] : Wiley-Blackwell
    Materials and Corrosion/Werkstoffe und Korrosion 42 (1991), S. 403-409 
    ISSN: 0947-5117
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Description / Table of Contents: Korrosionsmechanismen von gesintertem nichtrostendem Stahl (AISI 316L) in NatriumchloridlösungDas elektrochemische Verhalten eines gesinterten nichtrostenden Stahls wurde mit dem von Schmiedematerial derselben Zusammensetzung verglichen. Die elektrochemischen Messungen umfaßten die Änderung des Korrosionspotentials mit der Zeit, die anodische und kathodische Polarisation und die Strom/Zeit-Transienten. Ein weiterer Vergleich erstreckte sich auf die Sinterlegierung vor und nach Stabilisierung des Korrosionspotentials. Die geringe Korrosionsbeständigkeit des gesinterten nichtrostenden Stahls ist bedingt durch die Bildung eines Elements zwischen der freien Oberfläche und der inneren Oberfläche der untereinander verbundenen Poren. Die freie (äußere) Oberfläche wird demnach durch die Poren kathodisch geschützt, während innerhalb der Poren, wegen der Größe der reaktionsfähigen Oberfläche, die Korrosion verstärkt wird.
    Notes: The electrochemical behaviour of a sintered stainless steel and of a wrought AISI type stainless steel of the same composition were compared. The electrochemical measurements used were the evolution of the corrosion potential vs time, the anodic and cathodic polarizations and the current-time transients. Comparisons were also performed for the sintered alloy before and after stabilization of the corrosion potential. The low corrosion resistance of the sintered stainless steel is due to the formation of a galvanic couple between the free surface and the inside of the interconnected pores. Hence the free surface is cathodically protected by the pores, but reciprocally the corrosion increases inside the pores where the reactive area is very large.
    Additional Material: 12 Ill.
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  • 3
    ISSN: 0323-7648
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Der Einfluß der Art des Lösungsmittels auf die Bildungsgeschwindigkeit von 2-Difurfurylidenketon bei Verwendung von Wasser, Methanol, Ethanol und Propanol als Katalysatorlösungsmittel wurde untersucht. Es wurde gefunden, daß die Reaktion in wäßriger Lösung wegen der geringen Löslichkeit der Reaktanten und der Zwischenprodukte sehr langsam abläuft.
    Notes: The influence of solvent nature upon the formation rate of 2-difurfurylidene ketone with the use of water, methanol, ethanol, and propanol as catalyst solvent was studied. It was verified that the reaction proceeds slowly in aqueous medium due to the low solubility of the reactants and intermediates.
    Additional Material: 2 Ill.
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  • 4
    ISSN: 0323-7648
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Das Verhalten von hochgequollenen Hydrogelen auf Basis eines Copolymers von Acrylsäure und Acrylamid in Lösungen von niedermolekularen Salzen wurde untersucht. Eine Erklärung für den Mechanismus des Gelkollaps und die Quellung in Lösungen verschiedener Salze wird gegeben. Die Abhängigkeiten der Sorptionsgeschwindigkeit und der Menge der sorbierten Cupferionen von der Teilchengröße des trockenen Pulvers sowie vom Quellungsgrad wurden festgestellt.
    Notes: The behaviour of highly swelling hydrogels based on a copolymer of acrylic acid and acrylamide has been studied in solutions of low molecular weight salts. An explanation of the mechanism for gel collapse and swelling in solutions of various metals is presented. The dependences of the sorption rate and the amount of sorbed copper ions on the particle size of the dry powder and on the swelling coefficient were established.
    Additional Material: 5 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 42 (1991), S. 1525-1535 
    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: Styrene-acrylic acid copolymers exhibit miscibility with various aliphatic, crystalline polyamides (e.g., nylon 6, 11, and 12) at 20% acrylic acid content in the copolymer. At 8% acrylic acid, phase separation is observed with the crystalline polyamides. At 14% acrylic acid, partial miscibility is observed with each polyamide, resulting in the Tg's of the constituents shifted toward the other constituent. The miscibility of the styrene-acrylic acid copolymers ( 〉 14 wt % AA) can be ascribed to hydrogen bonding interactions with the polyamides. Styrene-acrylic acid (20% AA) copolymers are miscible with other nylons with alternating amide orientation along the chain (e.g., nylon 6,6 and nylon 6,9). These samples tend to crosslink upon exposure to temperatures above the polyamide melting point unlike the nylon 6, 11, and 12 blends in which branching may only occur. Nylon 11/styrene-acrylic acid blends were chosen for crystallization rate studies. A melting point depression of nylon 11 occurs with addition of the styrene-acrylic acid (20% AA). The Flory-Huggins interaction parameter from the melting point depression is calculated to be -0.27. The crystallization rate of nylon 11 is significantly reduced with the addition of the miscible SAA copolymers (20% AA). The spherulitic growth rate equation predicts this behavior based on a Tg increase with SAA addition.
    Additional Material: 10 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 43 (1991), S. 951-966 
    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 use of zinc stearate as an ionic plasticizer has been demonstrated to function effectively in a segmented ionene cationomer thereby permitting its melt processability. The ionene polymer is prepared by reacting dimethylamino-terminated polytetramethylene oxide (PTMO) oligomers with various benzyl dihalide compounds, leading to a segmented cationomer. Since the unplasticized ionene polymer undergoes degradation near the softening temperature (ca. 180°C), an ionic plasticizer was incorporated as a means of lowering the softening temperature to prevent degradation and permit melt processability. Zinc stearate was utilized in this study as it has been demonstrated to function well in other ionomers (essentially anionomers) in this capacity. Through the utilization of melt rheological and solid-state morphological investigations, it has been clearly shown that zinc stearate will function effectively as an ionic plasticizer in these quite different ionomer materials by lowering the softening temperature to ca. 120°C, thereby permitting melt processability. In addition, due to the crystallization of the zinc stearate following cooling, this same species also serves to enhance the mechanical properties in the solid state.
    Additional Material: 15 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 43 (1991), S. 1315-1321 
    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: Novel 2,2′,6,6′-tetrabromo-3,3′,5,5′-tetramethyl-4,4′-biphenol (TBTMBP), and its epoxy derivatives, were synthesized to incorporate the stable meta-brominated phenol moiety into epoxy resin systems. In electronic encapsulation and laminate applications, epoxy systems derived from TBTMBP have exhibited superior hydrolytic and thermal stability as compared with the conventional ortho-brominated epoxy resins. These properties have resulted in an extended device life for semiconductors and a high Tg with excellent blister resistance for the printed circuit board, while meeting flame retardancy requirements as well.
    Additional Material: 6 Tab.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 43 (1991), S. 1999-2004 
    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: Wood-polymer composites (WPC) of Geronggang (GE; Cratoxylon arborescens), a light tropical hardwood, impregnated with methyl methacrylate (MMA) and styrene-co-acrylonitrile (3 : 2; STAN), were prepared by in situ polymerization using γ radiation or catalystheat treatment. The dynamic flexural storage modulus, E′, for oven-dried GE, moist GE, and GE-MMA and GE-STAN composites decreased with increasing temperature. The percentage decreases for GE with 10 and 16.5% moisture contents were 74.5 and 98.2%, respectively, which were higher than those for GE and GE composites, which ranged between 40 and 50%. The impregnated polymers were not as effective as water in acting as plasticizers, due to their nonpolar nature and much higher molecular weights. The α-transition peaks for moist GE and GE composites were more distinct and were shifted to lower temperatures than those for oven-dried GE. The values ranged between 75 and 150°C for moist GE and between 102 and 170°C for the GE composites. The α-transitions of the catalyst-heat-treated GE composites were lower than that of the radiation-induced counterparts. GE-STAN composites were also observed to have lower α-transition temperatures than those for GE-MMA for the respective treatment process, which seems to suggest that STAN interacted to a greater extent with cell wall components than did MMA.
    Additional Material: 4 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 43 (1991), S. 1659-1671 
    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: Polystyrenes, polyacrylates, and poly(3,4-isoprenes) incorporating the hexafluorodimethylcarbinol functionality have been synthesized, characterized, and tested as microsensor coatings on a surface acoustic wave (SAW) device for dimethyl methylphosphonate (DMMP) vapor absorption sensitivity. The syntheses involved monomer functionalization and polymerization or hexafluoroacetone reaction with preformed polymer. All fluoroalcohol functionalized polymer coatings displayed sub parts per million level sensitivity with the slope of the absorption isotherm steepest at low DMMP concentrations. The order of sensitivity for the isomeric polystyrene fluoroalcohols (meta 〉 para ≫ ortho) paralleled that of the relative free hydroxyl to hydrogen-bonded hydroxyl content. Strong hydrogen bonding between the fluoroalcohol polymers and DMMP vapor was observed by IR spectroscopy. Acylation of the fluoroalcohol group markedly reduced the DMMP sensitivity.
    Additional Material: 6 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 43 (1991), S. 2057-2065 
    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: Wood-polymer composites (WPC) of Geronggang (GE; Cratoxylon arborescens), a light tropical hardwood, impregnated with methyl methacrylate (MMA), styrene-co-acrylonitrile (3: 2; STAN), methyl methacrylate-co-bis (2-chloroethyl) vinyl phosphonate (3 : 1; MVP) and methyl methacrylate-co-bis (chloropropyl)-2-propene phosphonate (3:1;MPP), were prepared by in situ polymerization using γ-radiation or catalyst-heat treatment. Thermal characterization of these WPC by limiting oxygen index measurements (LOI), thermogravimetry (TG), and differential scanning calorimetry (DSC) showed that the impregnants greatly modified the wood properties. The LOI values of the GE-MVP and GE-MPP composites were much higher than that for GE and the other composites, indicating the effectiveness of the phosphonates as flame retardants. Concomitantly, the flaming characteristics also compared favorably against that for GE and the other composites. The decomposition temperature and maximum rate of weight loss determined by TG for GE-MVP and GE-MPP were substantially reduced, whereas the char yields were greatly higher. These observations again indicate that phosphonates imparted flame-retarding properties to their composites. The thermal properties of GE-MMA and GE-STAN composites were not vastly different from that of untreated GE. Flame retardancy in the phosphonate-containing composites was effected through both the condensed- and gaseous-phase mechanisms due to the presence of phosphorus and chlorine, respectively. Indication of grafting of polymer to wood was found for GE-STAN, GE-MVP, and GE-MPP composites, but not for GE-MMA. Composites prepared by γ-radiation or by the catalyst-heat treatment had similar thermal characteristics.
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