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  • Polymer and Materials Science  (559)
  • FLUID MECHANICS AND HEAT TRANSFER  (147)
  • Inorganic Chemistry  (76)
  • 1985-1989  (782)
  • 1980-1984
  • 1925-1929
  • 1988  (380)
  • 1987  (402)
Collection
Keywords
Publisher
Years
  • 1985-1989  (782)
  • 1980-1984
  • 1925-1929
Year
  • 1
    Electronic Resource
    Electronic Resource
    Crystallinities of copolymers of ethylene and 1-alkenes (1988)
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 26 (1988), S. 1271-1286 
    Details
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Random copolymers of ethylene with 1-butene, 1-octene, and 1-octadecene have been prepared using a homogeneous vanadium-based catalyst system. Comonomer contents determined by 13C-NMR analysis of polymer solutions are in the range 1-10 mol%. Crystallinities were estimated by means of density measurements, x-ray diffraction, differential scanning calorimetry, laser Raman spectroscopy, and CPMAS 13C-NMR spectroscopy. The results are compared with those obtained for heterogeneous copolymers of ethylene containing 1-4 mol% 1-butene. As the comonomer content is increased, the crystallinity decreases. The dimension perpendicular to the 110 plane in orthorhombic crystallites decreases linearly with crystallinity. This decrease in crystallite size is accompanied by an increase in the size of the orthorhombic unit cell. For copolymers containing large amounts of 1-octene and 1-octadecene, a second crystalline form appears. Differences in estimates of crystallinity are discussed in terms of looser packing in highly branched copolymers and the extent to which the second crystalline form participates in the phase structure.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/polb.1988.090260611
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    Paper (German National Licenses)
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  • 2
    Electronic Resource
    Electronic Resource
    Thermal behavior of cast polyurethane elastomers (1988)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 35 (1988), S. 1803-1815 
    Details
    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: Thermal properties like glass transition temperature (Tg), initial decomposition temperature (idt), integral procedural decomposition temperature (ipdt), and temperature at various % weight loss of a number of polyurethane systems are reported in this paper. Glass transition temperature was determined on TMA, and other thermal properties were determined by thermogravimetry. The experiments were designed to understand various factors such as length of chain extender moiety, flexibility of chain extender units by substitution of ether link in the diol chain, nature of bonds (unsaturation) in the extender unit, and nature of diisocyanates.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1988.070350708
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  • 3
    Electronic Resource
    Electronic Resource
    Consistent values of rate parameters in free radical polymerization systems (1988)
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 26 (1988), S. 293-297 
    Details
    ISSN: 0887-6258
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pol.1988.140260704
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  • 4
    Electronic Resource
    Electronic Resource
    Ethylene polymerization over organochromium catalysts: A comparison between closed and open pentadienyl ligands (1987)
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 25 (1987), S. 2063-2075 
    Details
    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.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pola.1987.080250804
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  • 5
    Electronic Resource
    Electronic Resource
    Adsorption of low density lipoproteins onto selected biomedical polymers (1987)
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 21 (1987), S. 683-700 
    Details
    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.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/jbm.820210602
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  • 6
    Electronic Resource
    Electronic Resource
    A SIMS calibration exercise using multi-element (Cr, Fe and Zn) implanted GaAs (1987)
    Chichester [u.a.] : Wiley-Blackwell
    Surface and Interface Analysis 10 (1987), S. 338-342 
    Details
    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.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/sia.740100705
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  • 7
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    Effects of multiple rows and noncircular orifices on dilution jet mixing (1987)
    In:  Other Sources
    Details
    Publication Date: 2011-08-19
    Keywords: FLUID MECHANICS AND HEAT TRANSFER
    Type: Journal of Propulsion and Power (ISSN 0748-4658); 3; 219-226
    Format: text
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    NASA TECHNICAL REPORTS
  • 8
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    Structure of unsteady flows at leading- and trailing-edges: Flow visualization and its interpretation (1987)
    In:  CASI
    Details
    Publication Date: 2017-10-02
    Description: Unsteady two- and three-dimensional flow structure at leading and trailing edges of bodies can be characterized effectively using recently developed techniques for acquisition and interpretation of flow visualization. The techniques addressed here include: flow image/surface pressure correlations; 3-D reconstruction of flow structure from flow images; and interactive interpretation of flow images with theoretical simulations. These techniques can be employed in conjunction with: visual correlation and ensemble-averaging, both within a given image and between images; recognition of patterns from images; and estimates of velocity eigenfunctions from images.
    Keywords: FLUID MECHANICS AND HEAT TRANSFER
    Type: AGARD, Aerodynamic and Related Hydrodynamic Studies Using Water Facilities; 13 p
    Format: text
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    NASA TECHNICAL REPORTS
  • 9
    Electronic Resource
    Electronic Resource
    Flame retardation of poly(ethylene terephthalate) containing poly(4-bromo styrene), poly(vinyl bromide), and poly(vinylidene bromide)Issued as NRCC No. 27244. (1987)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 33 (1987), S. 2041-2052 
    Details
    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.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1987.070330616
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  • 10
    Electronic Resource
    Electronic Resource
    Polymer compatibility and interpolymer association in the poly(acrylic acid)-polyacrylamide-water ternary system (1988)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 35 (1988), S. 707-716 
    Details
    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: Polyacrylamide and poly(acrylic acid) form a water-insoluble phase when solutions of the two having concentrations that are not too low are mixed. The insoluble complex contains nearly stoichiometric 1 : 1 ratios of acrylamide and acrylic acid. The phase behavior of the ternary system was studied as a function of the degree of neutralization, α, of poly(acrylic acid). The complex is not formed when α is high. The formation of the complex was studied by measurement of pH increases observed when poly(acrylic acid) was titrated with polyacrylamide to infer a degree of linkage, θ, between the two polymers. A Hill plot of the data showed that the association was cooperative when the molecular weight was high.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1988.070350311
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