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  • Polymer and Materials Science  (278)
  • SPACE RADIATION  (135)
  • Physics  (73)
  • STRUCTURAL MECHANICS  (72)
  • ASTROPHYSICS
  • 1970-1974  (345)
  • 1960-1964  (140)
  • 1972  (345)
  • 1963  (140)
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  • 1970-1974  (345)
  • 1960-1964  (140)
Year
  • 11
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 6 (1972), S. 405-441 
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: Porcelain inlays coupled by a silane treatment to composite resins which were used as cementing media and in turn retained by an undercut were evaluated as to their marginal integrity and retention against conventionally restored teeth. These included restorations in teeth with undercuts of resins, composites, and porcelain inlays cemented with zinc oxyphosphate cements.The evaluations were determined by isotope penetration during thermal cycling (180 cycles from 12 to 50°C), scanning electron microscopy of sectioned restorations, and mechanical pull tests.The results showed improved retentive qualities and markedly improved resistance to marginal penetration. Improved adaptation of the composite to the tooth surface was produced by the mechanical action of seating the porcelain inlay.
    Additional Material: 29 Ill.
    Type of Medium: Electronic Resource
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  • 12
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 6 (1972), S. 413-423 
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: The effect of surface contamination on the morphology and orientation of poly-L-alanine on a glass-ceramic and the (1010) and (1011) crystal faces of L-quart is dealt with both microscopically and graphically. “Cleaning” with an r. f. plasma cleaner and contamination with pure nitrogen results in a change in the number of active sites with a corresponding change in the relative orientation of the polymer and the strength of bonding.
    Additional Material: 7 Ill.
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  • 13
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Letters 10 (1972), S. 415-421 
    ISSN: 0449-2986
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 14
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Letters 1 (1963), S. 77-78 
    ISSN: 0449-2986
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 15
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Letters 10 (1972), S. 327-340 
    ISSN: 0449-2986
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 7 Ill.
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  • 16
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Letters 10 (1972), S. 409-414 
    ISSN: 0449-2986
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 3 Ill.
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  • 17
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 10 (1972), S. 2621-2637 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Chromocene deposited on silica supports of high surface area forms a highly active catalyst for polymerization of ethylene. Polymerization is believed to occur by a coordinated anionic mechanism previously outlined. The catalyst formation step liberates cyclopentadiene and leads to a new divalent chromium species containing a cyclopentadienyl ligand. The catalyst has a very high chain-transfer response to hydrogen which permits facile preparation of a full range of molecular weights. Catalyst activity increases with an increase in silica dehydration temperature, chromium content on silica, and ethylene reaction pressure. The temperature-activity profile is characterized by a maximum near 60°C, presumably caused by a deactivation mechanism involving silica hydroxyl groups. A value of 72 was estimated for the ethylene-propylene reactivity ratio (r1). Linear, highly saturated polymers are normally prepared below 100°C. By contrast with other commercial polyethylenes, the chromocene catalyst produces polyethylenes of relatively narrow molecular weight distribution. Above 100°C, unsaturated, branched polymers or oligomers are formed by a simultaneous polymerization-isomerization process.
    Additional Material: 3 Ill.
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  • 18
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Letters 10 (1972), S. 561-567 
    ISSN: 0449-2986
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 3 Ill.
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  • 19
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A: General Papers 1 (1963), S. 951-964 
    ISSN: 0449-2951
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A study was made of the effect of polymerization temperature on the syndiotacticity of polyvinyl formate. Vinyl formate was polymerized with ultraviolet light initiation in the temperature range from -20 to +30°C. The value of (Ep  -  Et)/2 obtained, 4.5 kcal./mole, is characteristic of those values obtained by other workers for the free radical-initiated polymerization of vinyl acetate. A linear relationship was found to exist between the viscosities of the polyvinyl formates and those of the derived polyvinyl alcohols. The degree of polymerization of polyvinyl formate may be calculated from the equation: [η] = 4.42 × 10-3 DP0.63. The low temperature polymerization of vinyl for- mate results in more syndiotactic polymer, as shown by x-ray diffraction. Polyvinyl for-mate obtained at more elevated polymerization temperatures did not demonstrate the same degree of order. No difference was found between the infrared spectra of the polyvinyl formates. The polyvinyl alcohol derived from polyvinyl formate polymerized at low temperatures (0 to -35°C.) exhibits water resistance and forms a colored iodine complex similar to that obtained with the syndioactic polyvinyl alcohol derived from polyvinyl trifluoroacetate. Conventional polyvinyl alcohol and that derived from polyvinyl acetate polymerized at -30°C. do not exhibit the same properties. Minor differences in the 1,2-glycol content in the various polyvinyl alcohols do not account for the differences in the observations. The amount of head-to-head addition in various vinyl aliphatic esters seems to be related to the inductive strength of the acid portion of the ester. No difference was found between the crystallinities of the various polyvinyl alcohols, as measured by film density. Heat treatment increases the crystallinities about the same amount, but the water resistance of the stereoregular materials remains higher. From the good correlation between the observations made on polyvinyl formate and the derived polyvinyl alcohol, it is concluded that syndiotactic polyvinyl formate, and hence syndiotactic polyvinyl alcohol, is obtained by the low temperature free radical-initiated polymerization of vinyl formate. Increased syndiotacticity is more readily obtained in polyvinyl formate than in polyvinyl acetate, indicating the greater influence of inductive effect compared with the steric effect in controlling stereoregularity during free-radical propagation.
    Additional Material: 5 Ill.
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  • 20
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The stereochemical composition of the free radical alternating isobutene-maleic anhydride (IB/MA), isobutene-dimethyl fumarate (IB/DMF), and isobutene-dimethyl maleate (IB/DMM) copolymers was investigated by proton magnetic resonance. In contrast to the singlet gem-dimethyl resonance found in polyisobutene or in the alternating isobutene/acrylonitrile copolymer, the gem-dimethyl resonance of IB/MA, hydrolyzed IB/MA, and esterified IB/MA is a quadruplet with peaks of approximately equal intensity. The multiplicity of the spectra is consistent with the presence of equal amounts of threo-di-isotactic and threo-di-syndiotactic triads, disproving previous claims that such copolymers are predominantly threo-di-isotactic. The spectrum of the analogous IB/DMF indicates that the copolymer is composed entirely of erythro-di- isotactic and erythro-di-syndiotactic triads. This result is consistent with the exclusive trans opening of the dimethyl fumarate double bond and provides the first example for the stereospecific double bond opening of a noncyclic monomer in free radical polymerization. In contrast, the spectrum of IB/DMM shows that the dimethyl maleate double bond opens approximately 93% cis and 7% trans during copolymerization. Since the stereochemical composition of IB/DMF and IB/DMM is not the same, it is concluded that the radicals formed from dimethyl maleate and/or dimethyl fumarate do not equilibrate freely among all the possible configurations before isobutene addition.
    Additional Material: 6 Ill.
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