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  • Physics  (34)
  • ossification of the posterior longitudinal ligament  (1)
  • 1
    ISSN: 1436-2023
    Keywords: Key words: bone histomorphometry ; iliac bone biopsy ; ossification of the posterior longitudinal ligament
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract: To investigate whether there was any abnormal systemic bone metabolism in patients with ossification of the posterior longitudinal ligament (OPLL), we measured various histomorphometric indices of the iliac trabecular bones in 19 patients with OPLL (14 men, 5 women). For each index, the Z-score for each patient was calculated, using the SD and mean value for non-OPLL control group (n = 159) who underwent orthopaedic surgeries and had no systemic disease, age-matched for each decade. A Z-score of 1.0 meant that the observed data deviated 1 SD from the normal average, and a distribution from −2 to +2 was considered normal. All the averaged Z-scores were within ±1.0 and there were no significant differences between the OPLL and the control groups. There was also no difference in Z-score among three types of OPLL (segmental, continuous, and mixed). From these results, we concluded that there was no common abnormal bone metabolism affecting the bone histomorphometry of the iliac bone in OPLL patients. However, in two patients, the Z-score for bone volume (BV/TV) was more than 2.0, with increased osteoid volume (OV/TV) and increased trabecular thickness, suggesting that there was some abnormal bone metabolism in these two patients with OPLL.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 815-820 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Photopolymerization of cyclohexene oxide in the presence of electron acceptors was studied in a bulk system (in liquid as well as in solid states). The polymerization was proved to proceed by a cationic mechanism in both states by the effect of inhibitors. In a liquid phase the light intensity dependence of the rate of polymerization and the molecular weight distribution showed a contribution of a free ionic polymerization. Any discontinuous phenomenon in the rate as well as in the molecular weight was not discerned between liquid(above -36°C) and plastic crystal (between -36 and -81°C) phases. A quantum yield of monomer consumption as high as 8 × 103 was observed in the plastic crystal phase. Below -81°C in the normal crystal phase the rate as well as the molecular weight was remarkably suppressed.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 20 (1982), S. 1709-1716 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Radiation-induced cationic polymerization of styrene was studied in methylene chloride in the presence of triphenylsulfonium hexafluorophosphate. Acceleration in polymerization and an increase in molecular weight at a low temperature (-78°C) were observed in the presence of triphenylsulfonium salt. A study of pulse radiolysis revealed that both effects are due mainly to PF-6, which forms ion pairs with the cationic species involved in the polymerization.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 1859-1865 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Photopolymerization of a mixture of cyclohexene oxide and nitroethylene was carried out with the purpose of carrying out cationic and anionic polymerizations simultaneously in the same system. The excitation of the charge transfer band by light of wavelength longer than 390 nm gives rise to the polymerization of both monomers. No polymer was obtained in the dark. Additives affect the composition of the polymer, the rates of polymerization, and the molecular weight distributions. These data show that cationic polymerization of cyclohexene oxide and anionic polymerization of nitroethylene occurs simultaneously in this system.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The effect of homogeneity of polymerization phase and monomer concentration on the temperature dependence of initial polymerization rate was studied in the radiation-induced radical polymerization of binary systems consisting of glass-forming monomer and solvent. In the polymerization of a completely homogeneous system such as HEMA-propylene glycol, a maximum and a minimum in polymerization rates as a function of temperature, characteristic of the polymerization in glass-forming systems, were observed for all monomer concentrations. However, in the heterogeneous polymerization systems such as HEMA-triacetin and HEMA-isoamyl acetate, maximum and minimum rates were observed in monomer-rich compositions but not at low monomer concentrations. Furthermore, in the HEMA-dioctyl phthalate polymerization system, which is extremely heterogeneous, no maximum and minimum rates were observed at any monomer concentration. The effect of conversion on the temperature dependence of polymerization rate in homogeneous bulk polymerization of HEMA and GMA was investigated. Maximum and minimum rates were observed clearly in conversions less than 10% in the case of HEMA and less than 50% in the case of GMA, but the maximum and minimum changed to a mere inflection in the curve at higher conversions. A similar effect of polymer concentration on the temperature dependence of polymerization rate in the GMA-poly(methyl methacrylate) system were also observed. It is deduced that the change in temperature dependence of polymerization rate is attributed to the decrease in contribution of mutual termination reaction of growing chain radicals to the polymerization rate.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 1149-1156 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The radiation-induced polymerization of binary systems consisting of glass-forming monomer and glass-forming solvent in supercooled phase was studied. The initial polymerization rates were markedly affected by Tg (glass transition temperature) and Tv of the system (30-50°C higher than Tg), which turned to be functions of the composition. The composition and temperature dependence of initial polymerization rate in binary glass-forming systems were much affected by homogeneity of the polymerization system and the Tg of the glass-forming solvent. The composition and temperature dependences in the glycidyl methacrylate-triacetin system as a typical homogeneous polymerization system were studied in detail, and the polymerizations of hydroxyethyl methacrylate-triacetin and hydroxyethyl methacrylate-isoamyl acetate systems were studied for the heterogeneous polymerization systems; the former illustrates the combination of lower Tg monomer and higher Tg solvent and the latter typifies a system consisting of higher Tg monomer and lower Tg solvent. All experimental results for the composition and temperature dependence of initial polymerization rate in binary glass-forming systems could be explained by considering the product of the effect of the physical effect relating to Tv and Tg of the system and the effect of composition in normal solution polymerization at higher temperature, which was also the product of a dilution effect and a chemical or physical acceleration effect.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 1811-1818 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The effect of temperature and composition on the inflection point in the time-conversion curve and the saturated conversion was investigated in the radiation-induced radical polymerization of binary systems consisting of a glass-forming monomer and a solvent. In the polymerization of completely homogeneous systems such as glycidyl methacrylate (GMA)-triacetin and hydroxyethyl methacrylate (HEMA)-propylene glycol systems, the time-conversion curve has an inflection point at polymerization temperatures between Tvm (Tv of monomer system) and Tvp (Tv of polymer system). Such conversions at the inflection point changed monotonically between 0 and 100% in this temperature range. Tv was found to be 30-50°C higher than Tg (glass transition temperature) and a monotonic function of composition (monomer-polymer-solvent). The acceleration effect continued to 100% conversion above Tvp, and no acceleration effect was observed below Tvm. The saturated conversion in homogeneous systems changed monotonically between 0 and 100% for polymerization temperatures between Tgm (Tg of monomer system) and Tgp (Tg of polymer system). Tg was also a monotonic function of composition. No saturation in conversion was observed above Tgp, and no polymerization occurred below Tgm. In the polymerization of completely heterogeneous systems such as HEMA-dioctyl phthalate, no acceleration effect was observed at any temperature and composition. The saturated conversion was 100% above Tg of pure HEMA, and no polymerization occurred below this temperature in this system.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 13 (1975), S. 77-85 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Initiation and propagation mechanisms of the spontaneous polymerization of the system nitroethylene-isobutyl vinyl ether were studied. An equimolar mixture of these two monomers gives white precipitates below room temperature, though they react explosively to give viscous products at higher temperature. The precipitate was found to be composed of a polynitroethylene and a cycloadduct of these two monomers. The isolated cycloadduct product is so reactive that it not only polymerizes itself spontaneously but also initiates the polymerization of nitroethylene. The polymerization of the cycloadduct was revealed to proceed without termination to produce an alternate copolymer of these two monomers. These results indicate that the explosive spontaneous polymerization of this system consists of three elementary reaction processes; (1) cycloaddition reaction between two monomers, (2) anionic polymerization of nitroethylene induced by the cycloadduct, and (3) the living ring-opening polymerization of the cyclo-adduct.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 20 (1982), S. 2151-2158 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The radiation-induced cationic polymerization of styrene in methylene chloride is promoted by the addition of (C6H5)2IPF6, while the polymerization is inhibited in the presence of (C6H5)2ICl. The pulse radiolysis study reveals that both the yield and the lifetime of styrene dimer radical cation are increased by the addition of (C6H5)2IPF6, and, on the contrary, both are decreased in the presence of (C6H5)2ICl. The kinetic plots for the decay of the dimer radical cation in the presence and absence of the salts show that the decay is predominantly due to the neutralization with Cl-. The lengthening of the lifetime of the dimer radical cation in the presence of (C6H5)2IPF6 is believed to be due to the stabilization toward Cl- by the ion-pair formation with PF6-. Slow formation of the dimer radical cation was also observed in the presence of (C6H5)2IPF6, which is attributable to the oxidation of radical species by the salt followed by the charge transfer to monomer. Such a slow formation of radical cation in the presence of (C6H5)2IPF6 was confirmed with biphenyl in methylene chloride.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 4 (1966), S. 2028-2029 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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