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  • Polymer and Materials Science  (275)
  • LUNAR AND PLANETARY EXPLORATION  (111)
  • 1985-1989  (386)
  • 1980-1984
  • 1970-1974
  • 1950-1954
  • 1987  (386)
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  • 1985-1989  (386)
  • 1980-1984
  • 1970-1974
  • 1950-1954
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  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 25 (1987), S. 2063-2075 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Divalent organochromium compounds, Cr(Lig)2, often become active catalysts for the polymerization of ethylene when deposited onto an oxide carrier such as silica or aluminophosphate. Hydroxyl groups are thought to react, releasing one ligand and binding the chromium to the surface. The behavior of the catalyst is then governed by the remaining ligand and the type of carrier. In this study two types of ligands were investigated: cyclopentadienyl and its open ring analog dimethylpentadienyl. This small difference in the type of ligand produces a fundamental difference in the polymerization mechanism. For comparison the mixed ligand chromocene, with one open and one closed ligand, was also synthesized and tested for polymerization.
    Additional Material: 3 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 21 (1987), S. 683-700 
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: This study examines the interaction of human low density lipoprotein (LDL) with a select group of biomedical polymers. The adsorption characteristics of LDL on cured filler-free poly(dimethyl Siloxane) (C-PDMS), Biomer, Cardiomat 610, Kraton 1650, poly(hydroxyethyl methacrylate) (PHEMA) and glass are presented. Adsorption of LDL to charged hydrophilic glass control surfaces occurred rapidly, reaching plateau concentrations within one minute (0.19 ± 0.01 ug/cm2). Adsorption of LDL to polymer surfaces appeared to be dependent upon both the polymer hydrophobicity (or apolar nature), and flexibility (or dynamic nature) at the interface. Increased surface concentrations were observed for Biomer (0.32 ± 0.01 ug/cm2) as well as other polymers which exhibited both hydrophobic and elastomeric próperties. Temperature changes between 25°C and 37°C were found to significantly influence the surface concentration of LDL on Biomer (0.16 ± 0.01 ug/cm2 at 25°C versus 0.32 ± 0.01 ug/cm2 at 37°C). A lipid core phase transition at 36°C was believed to be responsible for the temperature influence. Preliminary competitive adsorption studies of LDL with albumin (HSA) and serum on silicone surfaces suggests that LDL adsorption occurred rapidly and preferentially (0.25 ± 0.01 ug/cm2 for LDL alone; 0.33 ± 0.01 ug/cm2 for LDL + HSA; 0.15 ± 0.01 ug/cm2 LDL + serum). Preliminary studies on the role of LDL in calcification were not conclusive. It can be concluded that LDL adsorption is dependent upon polymer hydrophobicity, flexibility and temperature. Competitive adsorption experiments suggests that LDL may have substantial influence on protein adsorption.
    Additional Material: 10 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Surface and Interface Analysis 10 (1987), S. 338-342 
    ISSN: 0142-2421
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: Multi-element (52Cr, 56Fe and 66Zn) implanted GaAs samples have been prepared specially for SIMS calibration. Absolute chemical measurements gave retained ion doses which agreed to within 12% of the nominal implanted dose (2.0 × 1014 atoms cm-2). Comparative SIMS depth profiles with five instruments gave Cr mode depth data which showed a variability of 5%. After data normalization to a common mode depth (168 nm) the shape of all profiles showed good agreement. SIMS anàlysis of similar samples containing lower dose implants (1.0 × 1013 atoms cm-2) showed that ∼50% of the Cr was contained in the near surface region (0-0.03 μm). This surface peak was not observed in profiles of samples which had been singly implanted with Cr. It is proposed that the Cr surface peak results from radiation enhanced out-diffusion initiated by the subsequent Fe implant. Whilst the high dose multi-implant samples showed a similar Cr surface accumulation, its magnitude in relation to the ion implanted dose, was smaller. These samples therefore form reliable calibration specimens for the simultaneous determination of the secondary ion responses of Cr, Fe and Zn in GaAs.
    Additional Material: 4 Ill.
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  • 4
    Publication Date: 2019-07-12
    Description: Observations of electrostatic waves in the magnetosphere of Uranus are discussed with attention focused on the Bernstein emissions. The most intense Bernstein waves were observed near the magnetic equator of the planet, even though the tilt of the Uranian magnetic moment is very large relative to the rotational axis. In addition to the Bernstein modes, a number of highly sporadic emissions were detected in the vicinity of the Miranda L shell.
    Keywords: LUNAR AND PLANETARY EXPLORATION
    Type: Journal of Geophysical Research (ISSN 0148-0227); 92; 15225-15
    Format: text
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  • 5
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 25 (1987), S. 1825-1846 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The thermal degradation behavior of polyacrylamide and poly(acrylamide-co-acrylate) was studied by differential scanning calorimetry, thermogravimetric analysis, gas chromatography/mass spectrometry, and carbon-13 solid state nuclear magnetic resonance. The degradation products over the temperature range of 115-450°C were characterized. Mechanisms are proposed for the degradation processes involved.
    Additional Material: 18 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 25 (1987), S. 2643-2664 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The rapid defluorination of fluoropolymer surfaces by their exposure to a hydrogen plasma excited by an inductively coupled RF field has been studied using ESCA. The results are interpreted in terms of a reaction/depth profile; the reaction is not uniform with depth leading to the formation of an approximately 20 Å thick boundary layer of defluorinated material.
    Additional Material: 11 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 25 (1987), S. 3105-3115 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Melting points of copolymers of ethylene and 1-alkenes ranging from 1-butene to 1-octadecene have been determined. The copolymers were prepared by means of a homogeneous Et3Al2Cl3/VOCl3 initiating system so that in individual samples, comonomer contents do not vary with molecular weight. Evidence is presented for a random distribution of comonomer units in the copolymers. Melting points determined by differential scanning calorimetry are essentially independent of branch length at low comonomer contents. At higher comonomer contents (5-9 mol% 1-alkene), melting points decrease in the order 1-butene 〉 1-octene 〉 1-octadecene copolymers. The weight fraction of ethylene sequences drops to less than 60% in copolymers with 1-octadecene of high comonomer content and this results in a reduction in the crystallite thicknesses attained by these copolymers.
    Additional Material: 5 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 33 (1987), S. 2333-2344 
    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 simple, activity-based solution model is used to develop thermodynamically proper correlation forms for the description of the rate and equilibrium behavior of nonideal polyamidations. The approach is especially useful in systems for which limited equilibrium and kinetic data are available. This model is applied to the nylon 6,6 system. the resulting correlation is valid for water concentrations from 1 to 90 mol% and for temperatures from 200 to 265°C. The equilibrium correlation is a function of the water mole fraction and temperature. At a fixed temperature, there is a maximum in the apparent equilibrium constant at a water concentration of approximately 10 mol%. There is an apparent inversion in the sign of the heat of amidation, as well as a continuous change in the apparent rate of polymerization from second to third order in carboxyl concentration at low water content.
    Additional Material: 7 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 34 (1987), S. 2345-2345 
    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
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 33 (1987), S. 2041-2052 
    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 pyrolysis and gaseous combustion of poly(ethylene terephthalate) (PET) incorporating poly(4-bromostyrene), poly(vinyl bromide), and poly(vinylidene bromide) has been studied using thermogravimetry, flammability limit evaluation, and hydrogen bromide (HBr) evolution techniques. The data obtained have been compared with limiting oxygen index (LOI) flammability data to elucidate flame retardation mechanisms. All the organo bromides studied (applied either via topical treatment or radiation grafting) released HBr on pyrolysis which is capable of inhibiting the gas phase combustion reactions. Condensed phase interactions were also detected which were capable of altering the gaseous pyrolysates. Thermal stability considerations suggest that, although the aliphatic bromides are excellent sources of HBr, they are not ideal flame retardants for PET.
    Additional Material: 5 Ill.
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