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  • 1
    Electronic Resource
    Electronic Resource
    A calculation relating galvanism and marginal breakdown (1976)
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 10 (1976), S. 971-973 
    Details
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/jbm.820100614
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  • 2
    Electronic Resource
    Electronic Resource
    Initial adsorption of trimethylsilane on Ge(100) surfaces (1998)
    Chichester [u.a.] : Wiley-Blackwell
    Surface and Interface Analysis 26 (1998), S. 113-120 
    Details
    ISSN: 0142-2421
    Keywords: XPS ; x-ray photoelectron spectroscopy ; Ge ; adsorption ; trimethylsilane ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: Trimethylsilane (TMSiH) was adsorbed onto a Ge(100) surface at a temperature of -150±3°C and x-ray photoelectron spectroscopy (XPS) was used to study the resulting surface species as functions of the TMSiH exposure in Langmuir (L). The core-level C 1s, Si 2p and Ge 3d photoelectrons were monitored after each dosing. It was observed that the C-C bonds are the dominant species formed at the low doses of TMSiH. The second abundant species at the low coverage is the C-Ge bond. This indicated dissociative adsorption of TMSiH molecules onto a clean Ge(100) surface, which is similar to the adsorption of TMSiH molecules onto an Si(100) surface. As the dose increases, the Si-C species gradually increase due to physisorbed TMSiH on top of the C-C- and C-Ge-covered surface. This study clearly reveals the growth processes of TMSiH on a Ge(100) surface. The electronegativities of C, Si and Ge and the bond strengths of C-C, C-Si and C-Ge were invoked to discuss the initial formation of C-C and C-Ge on the Ge(100) surface. © 1998 John Wiley & Sons, Ltd.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Kinetics of sol-to-gel transition for poloxamer polyols (1991)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 43 (1991), S. 283-292 
    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: Kinetics of gelation for aqueous solutions of poloxamers 407 and 288 were determined using pulse shearometry. The principle of this method for determining the shear modulus of a semisolid was based on generation of a torsional force that is transmitted through the poloxamer sample at discrete time intervals. Three distinct linear phases were observed for the log dynamic shear modulus (G′) vs. time profiles as poloxamer 407 and 288 solutions of varying concentrations were allowed to passively warm at room temperature to a temperature exceeding the sol-to-gel transition temperature, Tm. The beginning of the second exponential phase coincided with the onset of the gelation process as determined by visual observation. Although gelation appeared visually to be complete at the beginning of the third exponential phase of the log G′ vs. time profiles, this last exponential phase may indicate the rate of formation of the polymer network. A comparison of poloxamer 407 [30% (w/w); Tm = 10.9°C] and poloxamer 288 [37% (w/w); Tm = 11.1°C] would suggest that the concentration of poloxamer required to achieve approximately the same gelation temperature for poloxamers having a similar ratio of poly(oxypropylene):poly(oxyethylene) units decreases with increasing molecular weight of the poly(oxypropylene) hydrophobe contained in the copolymer. Results of these preliminary studies suggest that the gelation process was significantly (p 〈 .05) more rapid for poloxamer 407 at a 30% (w/w) concentration compared to a 30% (w/w) solution of poloxamer 288 when the poloxamer solutions were allowed to passively warm at room temperature. In addition, it appears that the rate of gelation for the poloxamer solutions studied was dependent on the rate of heat transfer through the polymer solution.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1991.070430207
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  • 4
    Electronic Resource
    Electronic Resource
    Physical modification of polyacrylonitrile precursor fiber: Its effect on mechanical properties (1994)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 52 (1994), S. 1667-1674 
    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: Polyacrylonitrile precursor fiber of a special grade for making carbon fibers was modified by stretching in the prestabilization stage to various extents. The effect of such stretching on tensile properties of the original precursor fiber, intermediate (oxidized) fiber, and resultant carbon fiber prepared through a continuous process was monitored. Improvements in tensile modulus of fibers at various stages were observed with increasing stretch ratios. However, no obvious enhancement of tensile strength of final carbon fibers was found. © 1994 John Wiley & Sons, Inc.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1994.070521201
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  • 5
    Electronic Resource
    Electronic Resource
    Conversion of polyacrylonitrile fibers to activated carbon fibers: Effect of activation (1996)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 60 (1996), S. 923-929 
    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: Polyacrylonitrile (PAN)-based activated carbon fibers were developed with the idea of increasing their potential and efficiency in industrial applications. The PAN-based fibers were first oxidized in air in a continuous multistage stabilization process, and then subjected to a continuous, low temperature carbonization and activation treatment in a mixture of steam and argon. The effect of the activation condition on the specific surface area, elemental composition, as well as the morphological structure of activated carbon fibers was studied. The surface area of the carbon fibers increased remarkably after the steam activation. It was found that steam activation promoted the elimination of nitrogen from the fiber. The bulk oxygen content of the fibers increased upon activation, probably due to formation of carbon-oxygen functionalities on the surface of the activated carbon fibers. The surface oxygen level of activated carbon fibers was greater than the bulk analysis of oxygen. It was observed that activation decayed the order of the carbon structure. © 1996 John Wiley & Sons, Inc.
    Additional Material: 3 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Continuous carbonization of polyacrylonitrile-based oxidized fibers: Aspects on mechanical properties and morphological structure (1994)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 52 (1994), S. 945-950 
    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: By following the progression of continuous carbonization (300-1250°C) of polyacrylonitrile (PAN)-based oxidized fibers, variations in tensile mechanical properties and morphological structure are reported in detail along the carbonization line. The tensile strength and Young's modulus of the fibers generally increase throughout the carbonization stage. Meanwhile, the fiber diameter displays a significant decrease. The preferred orientation of carbon layer planes is observed to increase remarkably for temperatures over 400°C. In a similar manner, the stacking size increases significantly but reaches saturation around 600°C, a changing point corresponding to that observed for the variation of the Young's modulus. However, beyond about 1200°C, the stacking size again displays a marked increase. Results thus obtained are interpreted in relation to each other. Possible implications are also discussed. © 1994 John Wiley & Sons, Inc.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1994.070520712
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  • 7
    Electronic Resource
    Electronic Resource
    Conversion of polyacrylonitrile fibers to activated carbon fibers: Effect of preoxidation extent (1996)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 62 (1996), S. 1771-1773 
    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
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1996.070621031
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  • 8
    Electronic Resource
    Electronic Resource
    Aspects on interaction between multistage stabilization of polyacrylonitrile precursor and mechanical properties of carbon fibers (1995)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 56 (1995), S. 289-300 
    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 progression of polyacrylonitrile (PAN) fibers on multistage stabilization stage has been monitored by following the variations in density, elemental composition, morphological aspect, and mechanical properties. The effects of various processing conditions during the multistage stabilization on the mechanical properties of final carbon fibers were evaluated in detail. To achieve an optimal extent of stabilization of PAN fibers is critical as the final mechanical properties of carbon fibers are concerned. This aim can be realized by adjusting and matching the temperatures in each step and the processing rates during multistage stabilization. Imposing stretching on multistage stabilization is beneficial to mechanical properties of carbon fibers. © 1995 John Wiley & Sons, Inc.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1995.070560221
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  • 9
    Electronic Resource
    Electronic Resource
    Surface analyses of polyacrylonitrile-based activated carbon fibers by X-ray photoelectron spectroscopy (1996)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 62 (1996), S. 1987-1991 
    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: In this work, polyacrylonitrile (PAN)-based activated carbon fibers (ACFs) were developed by the common processes of stabilization, carbonization, and steam activation. Those fibers were successively subjected to heat treatment in a vacuum at high temperature and reactivation in steam. The changes in specific surface area and surface chemical characteristics were studied. The vaccum treatment reduced the surface area dramatically, while the surface nitrogen decreased after activation in steam and the surface oxygen was lowered upon the vaccum treatment. By curve-fitting the X-ray photoelectron spectroscopy (XPS) of C1s, O1s, and N1s, it was shown that the forms and compositions of the oxygen-containing functionalities seemed not to be affected significantly by the above-mentioned heat-treat-ment processes, whereas the nitrogen-containing functionalities showed some changes with these treatments. © 1996 John Wiley & Sons, Inc.
    Additional Material: 4 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Adhesion of synthetic organic polymer on soft tissue. I. A fast setting polyurethane adhesivePresented in part at the 165th National Meeting, American Chemical Society, Dallas, Texas, 1973. (1974)
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 8 (1974), S. 35-43 
    Details
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: Conventional polyurethane prepolymers have been shown to adhere to living biological tissues. However, their setting is not sufficiently expedient to permit convenient applications in vivo. A prepolymer prepared from the highly reactive 6-chloro-2,4,5-trifluoro-1,3-phenylene diisocyanate, castor oil, and a trace of pyridine has afforded an adhesive which sets in about 2 min in vivo. The fast setting has resulted in poor adhesion on biological tissue. The bonding has been improved by the inclusion of tolylene diisocyanate in the composition without affecting the fast curing rate of the prepolymer. The dispersion of the adhesive and its cohesion after solidification have been adjusted by other minor additives. Preliminary evaluation on animals indicates that this adhesive is most useful as a hemostatic coating in hepatic lacerations.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/jbm.820080105
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