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  • 1
    Electronic Resource
    Electronic Resource
    Role of Surface Effects in the Inelastic Background of X-ray Photoelectron Spectroscopy (1996)
    Chichester [u.a.] : Wiley-Blackwell
    Surface and Interface Analysis 24 (1996), S. 490-496 
    Details
    ISSN: 0142-2421
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: We have derived a new deconvolution formula to obtain the original no-loss XPS spectra, the so-called source function, by taking surface effects into account. With this formula the primary XPS spectra of Au 4d and Au 4f are carried out from the experimental data. The primary excitation spectra are compared to the results derived by Tougaard’s method in which surface effects were neglected. The present result is markedly different from Tougaard’s result, which consists of a tail extending ∽50 eV below the peak. The result reveals that the influence of surface effects on the background removal of the spectra is considerably significant for the energy range ∽50 eV below the peak energy. It is also found that the large tail in Tougaard’s results can be essentially removed when surface effects are considered.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Isolation and quantitative analysis of hydroxylysine glycosides (1989)
    Springer
    Chromatographia 28 (1989), S. 497-501 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Collagen metabolites ; Amino acid derivatives ; Glycosides
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Methods are described for the isolation of galactosyl hydroxylysine and glucosylgalactosyl hydroxylysine from collagen and for the quantitative analysis of these hydroxylysine glycosides. The isolation procedure, based upon gel filtration and preparative ionpaired reversed-phase high-performance liquid chromatography, is simple and rapid in comparison with existing methods, allowing the production of tens of milligrams of each glycoside in a single day. Quantitative analysis of the hydroxylysine glycosides is effected by reversed-phase high-performance liquid chromatography with precolumn derivatization (usingo-phthal-dialdehyde) and fluorescence detection.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02261068
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  • 3
    Electronic Resource
    Electronic Resource
    Characterization of azo-containing polydimethylsiloxanes and their copolymers with methyl methacrylate (1996)
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 34 (1996), S. 2613-2620 
    Details
    ISSN: 0887-624X
    Keywords: polydimethylsiloxane ; poly(methyl methacrylate) ; block copolymer ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Azo group-containing polydimethylsiloxanes (PDMS-ACP), macroazoinitiators, were prepared by polycondensation reaction of 4,4′-azobis-4-cyanopentanoyl chloride (ACPC) with hydroxybutyl-terminated polydimethylsiloxane (PDMS) of varying molecular weights. The activation energy (Ea), activation enthalpy (ΔH
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Role of surfactant in composite latex particle morphology (1992)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 45 (1992), S. 487-499 
    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: Composite particles were prepared by seeded emulsion polymerization at 70°C using K2S2O8 as initiator and two different nonionic surfactants. Monodisperse polystyrene latex particles were used as seed and methyl methacrylate was used as second-stage monomer. When the surfactant, polyethylene oxide-propylene oxide (Pluronic F-108), was used, the final particle morphology showed that the PMMA (core) was partially covered by polystyrene. However, when nonyphenol polyethylene oxide (Igepal Co-990) was used as surfactant, one observed a reversed type of encapsulation (i.e., PS core is partially engulfed by PMMA). The interfacial tensions of the polymer phase against water containing the appropriate surfactant were measured by the drop-volume method and used in a mathematical model based on thermodynamic analysis to predict the equilibrium particle morphology. The observed particle morphologies were found to differ from the predicted morphologies at low conversion of the second-stage monomer but agreed with it at higher conversion.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1992.070450313
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  • 5
    Electronic Resource
    Electronic Resource
    Characterization of carboxylated poly(butyl acrylate) latices produced by a semibatch process (1996)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 62 (1996), S. 585-594 
    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: Several carboxylated poly(butyl acrylate) latices prepared by a semibatch emulsion poly-merization process were characterized in this study. A significant amount of polyelectrolyte was found in the latex product containing 10% AA, designated as AA10. On the other hand, latices containing 0.1% AA (AA0.1), 0.1% MAA (MAAC.1), and 10% MAA (MAA10) showed very low levels of polyelectrolyte in water. Based on the critical flocculation concentration data, it can be concluded that incorporation of 10% AA or 10% MAA into the emulsion polymers can greatly improve the chemical stability of the latex products, especially at higher pH. The data of the pH and conductometric titration experiments show that the MAA unit can be distributed more uniformly in the latex particles in comparision with the AA unit. This result is further confirmed by determination of the Tg's of the emulsion polymers by means of thermally stimulated current (TSC). © 1996 John Wiley & Sons, Inc.
    Additional Material: 12 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    The effect of hexane treatment on the permeation of silicone-coated polyethersulfone membranesIssued as NRCC No. 31483. (1990)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 41 (1990), S. 2169-2176 
    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 polyethersulfone membranes were cast from casting solutions including poly(vinyl pyrrolidone) additive. The membranes were further dried, silicone-coated, and used for the permeation study with hydrogen and nitrogen gases. It has been found that solvent hexane which was included in the silicone rubber solution for surface coating increased the pore size on the membranes surface when poly(vinyl pyrrolidone) was present in the membrane. The above effect counteracted the pore size decrease by silicone coating, and, as a result, an H2/N2 permeability ratio of only 8.9 was achieved as compared with 28, which was obtained when the base polyethersulfone membrane was prepared from a casting solution without poly(vinyl pyrrolidone) additive.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1990.070410921
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  • 7
    Electronic Resource
    Electronic Resource
    The influence of molecular weight on the large deformation behavior of SBS triblock copolymer elastomers (1977)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 21 (1977), S. 629-643 
    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: Engineering stress-strain properties were determined for two polystyrene-polybutadiene-polystyrene (SBS) triblock copolymer elastomers, one consisting of blocks of molecular weight 7000/43000/7000 and the other, 16000/85000/17000. In addition, various blends of these two materials were prepared in order to vary the number-average molecular weight of the blocks in a systematic way while maintaining polystyrene content in the range of 25-28 wt %. Samples were solvent cast from benzene or benzene/heptane mixtures and annealed before testing. Ring specimens were extended to rupture at varying strain rates on an Instron tensile tester. Results indicate that number-average molecular weight has a marked influence on stress-strain behavior over the range of molecular weights and testing conditions employed. The observed behavior is consistent with a systematic increase in the proportion of a mixed interfacial region between the pure polystyrene and polybutadiene domain as molecular weight decreases. The interfacial region contributes to mechanical hystersis, rate sensitivity, and toughness in the SBS materials. Scanning electron photomicrographs of fracture surfaces also showed systematic changes with molecular weight.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1977.070210305
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  • 8
    Electronic Resource
    Electronic Resource
    Nylon 4/PVA blend membrane for dialysis (1991)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 43 (1991), S. 1795-1804 
    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: To improve the hydrophilicity and enhance the transport flux of nylon 4 membrane for dialysis, this study attempts to utilize blending nylon 4 with poly(vinyl alcohol) (PVA). The instability of PVA in water can be obtained more easily than by other methods, such as chemical, γ-ray irradiated crosslinking, or high-temperature treatment used by previous researchers. The effects of maturation time of the casting solution, nylon 4/PVA ratios, and casting solvent compositions on esterification of PVA, salt permeability, water content, partition coefficient, diffusivity, and mechanical strength of membrances are studied. The membrane, prepared by casting solution of nylon 4/PVA = 9/1 wt % formic acid with 24-h maturation time, possesses permeabilities of NaCl and urea, 33.14 and 19.67 × 10-5 cm2/min, respectively.
    Additional Material: 14 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1991.070431003
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  • 9
    Electronic Resource
    Electronic Resource
    Retention of fullerenes by octadecyl silica. Correlation with NMR spectra at low temperatures (1995)
    Springer
    Chromatographia 40 (1995), S. 507-512 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Fullerenes ; Retention vs NMR spectra ; C18 phases ; Low temperature separations
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The temperature effect on the retention of fullerenes in the range 80°C to −70°C in liquid chromatography (LC) has been examined using octadecylsilica stationary phases (ODS). It has been found that the maximum retention temperature lies around −10°C with a highly carbon loaded ODS phase. Solid state CPMAS NMR measurements on the stationary phases indicated that the relaxation time at the 30 ppm methylene signal changes with the temperature and has a minimum relaxation time at the temperature which closely matches the maximum retention temperature observed in chromatography. The interpretation of both NMR spectroscopic and LC chromatographic data are discussed.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02290260
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  • 10
    Electronic Resource
    Electronic Resource
    Effect of temperature on the mechanism of retention of fullerenes in liquid chromatography using various alkyl bonded stationary phases (1996)
    Springer
    Chromatographia 42 (1996), S. 56-62 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Fullerences ; Alkyl bonded silica phases ; Retention vs. column temperature ; CP-MAS NMR
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The temperature-dependency of the separation of fullerenes in liquid chromatography (LC) has been examined using various alkyl bonded stationary phases. It has been found that a maximum retention temperature exists with long alkyl bonded stationary phases, whereas there is no similar effect with the newly synthesized alkyl bonded phases which have two phenyl groups at the base of the bonded phase. The interpretation of the retention behavior of fullerenes in the low temperature region on alkyl bonded stationary phases is discussed using information obtained by CP-MAS solid-state NMR spectroscopy and LC.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02271056
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