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  • Polymer and Materials Science  (1,920)
  • 2005-2009
  • 1985-1989  (1,063)
  • 1970-1974  (857)
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  • 1
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 6 (1972), S. 59-79 
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: Advantages of a hollow-fiber hemodialyzer have been well described. The goal of this program was to provide a working model of a noncellulosic hollow fiber artificial kidney with nonthrombogenic blood-contacting surfaces, low blood-priming volume and low pressure drop, a satisfactory rate of urea transport, and high rate of ultrafiltration of water. Also, the reliability and utility of these devices was to be demonstrated through clinical evaluation.
    Additional Material: 9 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Acta Polymerica 36 (1985), S. 624-627 
    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: Unter Hernziehung unterschiedlicher Präparationsmethoden wurde die Struktur verdünnter und konzentrierter (0,01 bis 9,8%) Lösungen des starkettigen Polyamidohydrazid (PAH) mittels Elektronenmikroskopie in zwei Lösungsmitteln (DMSO und DMAA) untersucht. Beginnend mit der Konzentration 0,01% erfolgt unterschiedliche Strukturierung in diesen Lösungsmitteln, die bezüglich des Polymers eine unterschiedliche Güte aufweisen. Die Ergebnisse wurden früheren Untersuchungen zur Rheologie konzentrierter PAH-Lösungen in den genannten Lösungsmitteln gegenüber gestellt.
    Notes: The structure of dilute and concentrated solutions (0.01-9.8%) of rigid-chain polyamidohydrazide (PAH) in dimethylsulphoxide and dimethylacetamide was investigated by electron microscopy using various preparation techniques. Starting with a 0.01% concentration, PAH shows two distinct types of structuration in the solvents. The results are compared with previously studied rheological properties of PAH in these solvents.
    Additional Material: 5 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 23 (1989), S. 571-589 
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: This study was performed to test the feasibility of using a biodegradable delivery system for the local controlled release of sodium fluoride as a mechanism for the stimulation of local bone growth. Sodium fluoride grains were mixed with poly-DL-lactic acid (PLA), and the mixture was then dissolved in acetone. After driving off the solvent, sheets of this material were rolled into rods 3.2 mm in diameter and 28.6 mm long. These were inserted into the intramedullary canals of the right femora of adult New Zealand White rabbits. A sham implant, made the same way but containing no fluoride, was inserted into the contralateral left leg. The effects of three different concentrations of sodium fluoride, 0.125 g NaF/g PLA, 0.250 g NaF/g PLA, and 0.500 g NaF/g PLA, were determined after a 4-week implantation period. In a second set of experiments, the concentration was fixed at 0.500 g NaF/g PLA with implantation durations of 4, 8, and 16 weeks. Expressed in terms of property ratios (experimental/control), bending strengths of the femora were significantly raised in most groups with the notable exception of Group 3 (0.500 g NaF/g PLA, 4 weeks). Cross-sectional area ratios in the distal femora were increased in all groups compared to right/left values for a normal unoperated group (p 〈 0.05), with the highest ratio being 1.50 (SD = 0.44) for Group 4 (0.500 g NaF/g PLA, 8 weeks). Only Group 4 animals showed significant (p 〈 0.05) increases in midshaft area ratio and none had responses proximally. Growth rates, measured by sequential fluorochrome labeling of bone followed the area ratio data and were only significant for the distal femora.
    Additional Material: 7 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 24 (1986), S. 2541-2551 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Trichroic infrared absorption has been measured for oriented phase I poly(vinylidene fluoride). In addition to intensity differences, frequency shifts in the plane transverse to the draw direction are apparent. Shifts up to 10 cm-1 in one-way drawn phase I are found for the CF2 stretching vibration (880 cm-1) between the direction normal to the film surface (thickness direction) and the remaining directions. Annealing the highly oriented films produces no major changes in the unique three-dimensional structure. A model based on crystal defect structures is proposed to explain the unusual frequency shift behavior in the phase I PVDF. Possible conformations and a mechanism of formation of the defects are discussed.
    Additional Material: 11 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 445-454 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The fundamental vibrational frequencies of an isolated chain of cis-1,4-polybutadiene have been calculated. Infrared and polarized Raman data are used in the force constant refinement routine. The assignments of the vibrational frequencies are discussed in terms of the potential energy distribution.
    Additional Material: 5 Ill.
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  • 6
    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: Durch die Synthese von cyclischen Acrylaten wurde eine Reihe von Monomeren erhalten, die hohe Reaktivitäten der Copolymerisation bei gleichzeitiger Fähigkeit zur radikalischen Ringöffnungspolymerisation aufweisen. Sie wurden polymerisiert, um einen Pyruvatester in die Polymerkette einzuführen. Eine Reihe von Spiromethylencyclohexadienen wurde hergestellt, um neben der Carbonylgruppe und gespannten Ringen weitere Gruppen zu finden, die die radikalische Ringöffnungspolymerisation fördern. Bei ihrer Polymerisation wurden Polymere mit einer p-Phenylengruppe in der Kette erhalten.
    Notes: In order to find a series of monomers with high reactivities in copolymerization and still undergo free radical ringopening polymerization, a series of cyclic acrylates were synthesized and polymerized to insert a pyruvate ester into the backbone of the polymer. In order to discover groups other than the carbonyl groups and strained rings that would promote free radical ring-opening polymerization, a series of spiro methylenecyclohexadienes were prepared and polymerized to give a polymer with a p-phenylene group in the backbone.
    Additional Material: 1 Tab.
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  • 7
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Acrylonitrile (AN) was graft-polymerized onto gelatinized cationic starch (CS) possessing diethylaminoethyl ether groups by cerium (IV) initiation to give stable latexlike copolymer dispersions. Dispersions of the latex copolymers, having up to 50% grafted polyacrylonitrile (PAN), air- and heat-dry on glass to clear, adhesive films. Sonification of up to 8% dispersions at 20 Khz reduced their viscosities from 1500-3000 cP to 15-40 cP. Scanning electron microscopy revealed that both nonsonified and sonified dispersions consist of ball-like particles measuring about 0.05-0.15 μ in diameter when dry. The films are formed by coalescence of these particles. The degree to which AN grafts onto CS at ambient temperature is related to the nitrogen content of CS, gelatinization time of CS at 95°C, sequence of AN and cerium(IV) addition, concentration of cerium (IV), concentration of AN, and severity of reaction agitation. Number-average molecular weight values of PAN were about 106 when grafting was conducted under stirring and about 5 × 105 when conducted under shaking action.
    Additional Material: 3 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 1213-1224 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The synthetic details of solution polymerization in benzene and bulk polymerization of vinylferrocene are reported. In benzene solutions, with azobisisobutyronitrile (AIBN) as the initiator, small yields of low-polydispersity low molecular weight (M̄n ≃ 5000) polyvinylferrocene is obtained. However, high yields can be obtained by continuous or multiple AIBN addition. Higher molecular weight polymers and binodal polymers can be obtained as the monomer concentration is increased. In bulk polymerizations, yields of 80% can be obtained. The molecular weight increases as temperature decreases from 80 to 60°C in bulk polymerizations, and an increasing amount of insoluble polymer results. The soluble portion is often binodal, the higher molecular weight node consisting of an increasingly branched structure. Lower molecular weight polymer was readily fractionated into narrow fractions from benzene-methanol systems, but higher molecular weight polymer proved impossible to fractionate into narrow fractions due to branching.
    Additional Material: 3 Ill.
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  • 9
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Lithiated isopropylidene-telechelic polyisobutylenes (i.e., PIBs capped with end groups) are most interesting novel intermediates for further transformations, e.g., functionalization, polymerization. This report concerns model lithiation experiments of 2,4,4-trimethyl-1-pentene (TM1P) that guided us toward the subsequent quantitative lithiation of isopropylidene-telechelic PIBs. Thus, lithiation of TM1P with, n-, s-, and t-butyllithium, in the presence of various complexing agents (i.e., TMEDA, t-BuOK, 1,2-DPE, CH3OCH2CH2OCH3, THF, and 12-crown-4) followed by silylation with Me3SiCl (for the purpose of quantitation) gave three products: 2(trimethylsilylmethyl)-4,4-dimethyl-1-pentene (TM1P-Si), 2(trimethylsilylmethyl)-4,4-dimethyl-2-pentene (TM2P-Si2). The relative product composition strongly depends on the BuLi/complexing agent ratio and temperature. Among the different butyllithiums and complexing agents the best overall results were obtained with the s-BuLi/TMEDA combination. Complete lithiation of TM1P with minimum dilithiation was obtained using the molar ratio [s-BuLi]: [TMEDA]: [TM1P] = 2 : 2 : 1. The apparent activation energy of lithiation by s-BuLi/TMEDA was found to be 6.7 ± 0.8 kcal/mol. Guided by TM1P model experiments, quantitative monolithiation of isopropylidene-capped polyisobutylene (including ca. 4% chain and isomerization) was achieved using the molar ratio [s-BuLi] : [TMEDA] : [C—C] = 5 : 4 : 1.
    Additional Material: 10 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 25 (1987), S. 203-214 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The free radical polymerization of o-methacryloyloxybenzoic acid using acetone and benzene as solvents, in the interval 30-120°C, is investigated. The polymerization in benzene has a precipitant character. However, when acetone is used as solvent, at reaction temperatures higher than 60-70°C, the polymerization deviates from the classic free radical mechanism and, beside the addition of monomer molecules to growing chain ends, the release of salicylic acid and the formation of cyclic anhydride structures of glutaric type in the main chain has been detected. The microstructure of polymers obtained has also been studied by the transformation into the corresponding poly(methyl methacrylate)s.
    Additional Material: 6 Ill.
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