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  • Polymer and Materials Science  (186)
  • EARTH RESOURCES AND REMOTE SENSING
  • SPACE RADIATION
  • 1995-1999  (127)
  • 1960-1964  (68)
Collection
Publisher
Years
Year
  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 3 (1960), S. 213-223 
    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 interaction between a carbon black filler and styrene-butadiene rubber is increased if the material is heated after milling. This effect has been attributed to the polymeric free radicals which are presented after milling but which require a high temperature to increase their mobility to the point where they can react. The extent of interaction increases with time of heating and with the amount of milling before heating. The postulated mechanism is supported by the experimental activation energies and by the predictable influence of free radical scavengers on the system.
    Additional Material: 12 Ill.
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  • 2
    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: An improved cell which permits the measurement of permeabilities of membranes to gases over a wide range of temperatures and gas pressures is described. The measurements are made by the variable volume method, under constant pressure differential across the membrane. The cell lends itself particularly well to routine tests, because it does not require calibration or the use of vacuum techniques. The performance of the cell is discussed, and typical experimental results are presented. A modified permeability cell of the same type for high-pressure studies is also described. Measurements with this apparatus show that the rate of gas permeation obeys, in some cases, a single from of Fick's law, even under pressure differentials across the membrane as high as 800 psi (54 atm.). The paper also compares permeability data obtained by the variable volume and the variable pressure methods. The permeability of 0.002 in.-thick Alathon 15 polyethylene to oxygen and nitrogen was determined between 0 and 50°C. by the two methods, using the same sample of membrane in situ, and the measurements were found to agree within experimental error. Permeabilites of 0.010 in.-thick samples of Alathon 15 polyethylene to nitrogen, oxygen, helium, and carbon dioxide obtained in the same temperature range by the variable volume method were 15-30% higher than the corresponding data determined by the variable pressure method. This discrepancy could be due to the fact that the variable pressure measurements with the thicker membrances may not have been made under true steady-state conditions, although permeabilities were determined from apparently linear sections of permeated gas pressure vs. time curves. A critical re-examination of the methods used to determine permeability constants is suggested.
    Additional Material: 13 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 33 (1995), S. 853-862 
    ISSN: 0887-624X
    Keywords: peroxide crosslinking of LLDPE ; extraction and swelling measurements of crosslinked LLDPE ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Extraction and swelling experiments were carried out in order to measure the crosslinkability by dicumyl peroxide (DCP) of new homogeneous linear low-density polyethylenes (LLDPEs) with different molecular weight, branch content, and length of branches. Considering that the tertiary radicals are most probable macroradicals, our results indicate that tertiary carbons in LLDPEs could be either sites for scission reaction of effective coupling, depending upon degree of branching and to a lesser extent on degree of crosslinking. In the range of branching between 16 and n CH3/1000 C (n - 31 for low DCP concentration and decreases with DCP content approaching the value of 23 for the range above ca. 6 DCP moles per number average PE mole), the tertiary carbons seem to be rather the sites for effective coupling. In this range of branching an increase of crosslinkability with branch concentration and molecular weight of PE is due to the increase of crosslinking efficiency, but the scission probability is very low. At branch content exceeding the value of n CH3/1000 C, the dominant reaction on tertiary carbons is scission, leading to a small decrease of crosslinkability with increasing branch content. The possible mechanisms favoring tertiary carbons for either coupling or scission are discussed. © 1995 John Wiley & Sons, Inc.
    Additional Material: 9 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 33 (1995), S. 915-920 
    ISSN: 0887-624X
    Keywords: 1H NMR spectroscopy ; 13C NMR spectroscopy ; condensation water ; curing ; melamine ; formaldehyde ; resins ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 1H and 13C NMR have been used for the quantitative determination of methylene-ether bridges in melamine-formaldehyde (MF) resins. The amount of methylene-ether bridges was determined by 13C NMR from the number of monomethylolated amino groups consumed in the condensation reactions and is in agreement with that calculated from the condensation water contents. This latter method, which involves a combination of 1H and 13C NMR, is based on the amount of condensation water released during the formation of both methylene and methylene-ether bridges. © 1995 John Wiley & Sons, Inc.
    Additional Material: 4 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 34 (1996), S. 2363-2370 
    ISSN: 0887-624X
    Keywords: polyamides ; ester aminolysis ; nylon-6,6 ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A new route for nylon-6,6 synthesis has been studied. The process is grounded on the synthesis of an α-amino ω-ester monoamide precursor (AME-6,6) easily available in reacting in the bulk hexamethylene diamine and dimethyl adipate at a low temperature (T ≅ 50°C) preferably in the presence of a phenol derivative. In such conditions AME-6,6 precipitates with a very good yield (90-95%). One of the greatest advantages of AME-6,6 is to keep the stoichiometric balance for further polyamidation; that is not the case in other processes. Moreover AME-6,6 is very stable, e.g., even stored at room temperature under air during 50 days. Polyamides-6,6 have been obtained from AME-6,6 (used freshly prepared or after storage) in glass laboratory reactors by direct heating under vacuum (T = 270°C) with number-average molecular weights of roughly 20,000. © 1996 John Wiley & Sons, Inc.
    Additional Material: 8 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 34 (1996), S. 2439-2454 
    ISSN: 0887-624X
    Keywords: radiation ; nitrile rubber ; NMR ; ESR ; radicals ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The mechanism of radiation-induced structural changes in nitrile rubber with different acrylonitrile contents were investigated by ESR, NMR, and FTIR. To investigate new structures solid-state NMR methods had to be used due to crosslinking of the irradiated rubbers, and higher probe temperatures were used to obtain better resolution. The radicals generated on the acrylonitrile groups were found to abstract hydrogen from the adjacent butadiene units resulting in the formation of allylic radicals. These allylic radicals reacted to form intermolecular crosslinks and cyclisation. Cyclisation of the butadiene units were found to occur in the initial stages of the irradiation. Radiation yields of radicals increased with acrylonitrile content from 1.42, 1.58, to 2.42 for 18, 30, and 45% acrylonitrile rubbers. The radiation yields for intermolecular crosslinking were higher in rubbers with higher acrylonitrile contents, giving G values of 17.8, 21.3, and 24.5 for 18, 30, and 45% acrylonitrile rubbers, respectively. However, the crosslink clustering was found to be less in the rubbers with a higher acrylonitrile content. © 1996 John Wiley & Sons, Inc.
    Additional Material: 15 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 33 (1995), S. 949-955 
    ISSN: 0887-624X
    Keywords: linear low-density polyethylene ; side reactions during peroxide crosslinking of LLDPE ; FTIR measurements of sol fractions ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: FTIR measurements of sol fractions were carried out in order to assess side reactions during dicumyl peroxide (DCP) crosslinking of linear low density polyethylenes (LLDPEs) with homogeneous distribution of short chain branching. The changes of methyl and olefinic unsaturation concentration were measured as a function of degree of branching and DCP content. The changes of methyl and vinylidene concentration indicate that the scission probability has greater significance for the samples with initial branch content above 31 CH3/1000 C and increases with increasing DCP concentration. The analysis of trans-vinylene concentration indicates that the probability of disproportionation also increases with increasing DCP content. The changes of methyl concentration in the sol fraction of the sample containing initially ca. 23 CH3/1000 C with increasing DCP content could be interpreted using the dependence of crosslinking efficiency on branch content found previously for some range of branch concentration. © 1995 John Wiley & Sons, Inc.
    Additional Material: 9 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 35 (1997), S. 807-811 
    ISSN: 0887-624X
    Keywords: miniemulsion ; droplet nucleation ; oil-soluble initiator ; water-soluble inhibitor ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 5 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 247 (1997), S. 45-59 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: In this paper we reviewed some of our work on the photo induced coloration of Poly(p-phenylene sulfide) (PPS) and compared it to recent results obtained from the thermal treatment of resins that varied in molecular weight and ionic content. The results from this study suggest that coloration of amorphous PPS films after UV irradiation is caused by products different from those that cause coloration in semicrystalline PPS after thermoxidation. In addition, we found that polymer end group chemistry and resin molecular weights play important roles in the thermoxidative coloration of PPS, but only nominally influence the photooxidative coloration of the resin. PPS coloration may arise from the accumulation of specific, colored products (e.g., phenyl-phenyl moieties) and the possible presence of intermolecular aggregates. The mechanism and extent by which these structures occur in UV irradiated or heated PPS are likely dependent upon the polymer morphology of the samples tested.
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  • 10
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 2413-2421 
    ISSN: 0887-6266
    Keywords: positron annihilation ; polyimide ; ion implantation ; membrane ; permeability ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: 6FDA-pMDA polyimide membranes were implanted with 140 keV N+ ions to fluences between 2 × 1014 and 5 × 1015 cm-2. Variable energy positron annihilation spectra were taken and spectral features compared to previously reported changes in gas permeability and permselectivity of these membranes as a function of ion fluence. Positron data corroborate the explanation of these changes in terms of molecular damage caused by the implant: for fluences up to about 1 × 1015 cm-2, the concentration of irradiation-induced defects merely increases with implant fluence; while fluences exceeding this threshold value create a second type of positron annihilation site, thereby marking a distinct change in the structure of the polymer, which is responsible for the vast improvement of gas permselectivity data found at the same threshold fluence. PACS codes: 78.70.Bj - positron annihilation; 61.82.Pv - polymers, organic compounds; 61.72.Ww - doping and impurity implantation. © 1998 John Wiley & Sons, Inc. J. Polym. Sci. B Polym. Phys. 36: 2413-2421, 1998
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