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  • Polymer and Materials Science  (370)
  • 1995-1999  (370)
  • 1996  (370)
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  • 1995-1999  (370)
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  • 1
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: Although it is well accepted that implant success is dependent on various surface properties, little is known about the effect of surface roughness on cell metabolism or differentiation, or whether the effects vary with the maturational state of the cells interacting with the implant. In the current study, we examined the effect of titanium (Ti) surface roughness on chondrocyte proliferation, differentiation, and matrix synthesis using cells derived from known stages of endochondral development. Chondrocytes derived from the resting zone (RCs) and growth zone (GCs) of rat costochondral cartilage were cultured on Ti disks that were prepared as follows: HF-HNO3-treated and washed (PT); PT-treated and electropolished (EP); fine sand-blasted, HCl-H2SO4-etched, and washed (FA); coarse sand-blasted, HCl-H2SO4-etched, and washed (CA); or Ti plasma-sprayed (TPS). Based on surface analysis, the Ti surfaces were ranked from smoothest to roughest: EP, PT, FA, CA, and TPS. Cell proliferation was assessed by cell number and [3H]-thymidine incorporation, and RNA synthesis was assessed by [3H]-uridine incorporation. Differentiation was determined by alkaline phosphatase specific activity (AL-Pase). Matrix production was measured by [3H]-proline incorporation into collagenase-digestible (CDP) and noncollagenase-digestible (NCP) protein and by [35S]-sulfate incorporation into proteoglycan. GCs required two trypsinizations for complete removal from the culture disks; the number of cells released by the first trypsinization was generally decreased with increasing surface roughness while that released by the second trypsinization was increased. In RC cultures, cell number was similarly decreased on the rougher surfaces; only minimal numbers of RCs were released by a second trypsinization. [3H]-thymidine incorporation by RCs decreased with increasing surface roughness while that by GCs was increased. [3H]-Uridine incorporation by both GCs and RCs was greater on rough surfaces. Conversely, ALPase in the cell layer and isolated cells of both cell types was significantly decreased. GC CDP and NCP production was significantly decreased on rough surfaces while CDP production by RC cells was significantly decreased on smooth surfaces. [35S]-sulfate incorporation by RCs and GCs was decreased on all surfaces compared to tissue culture plastic. The results of this study indicate that surface roughness affects chondrocyte proliferation, differentiation, and matrix synthesis, and that this regulation is cell maturation dependent. © 1996 John Wiley & Sons, Inc.
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  • 2
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: Titanium (Ti) surface roughness affects proliferation, differentiation, and matrix production of MG-63 osteoblast-like cells. Cytokines and growth factors produced in the milieu surrounding an implant may also be influenced by its surface, thereby modulating the healing process. This study examined the effect of surface roughness on the production of two factors known to have potent effects on bone, prostaglandin E2 (PGE2) and transforming growth factor β1 (TGF-β1). MG-63 cells were cultured on Ti disks of varying roughness. The surfaces were ranked from smoothest to roughest: electropolished (EP), pretreated with hydrofluoric acid-nitric acid (PT), fine sand-blasted, etched with HCl and H2SO4, and washed (EA), coarse sand-blasted, etched with HCl and H2SO4, and washed (CA), and Ti plasma-sprayed (TPS). Cells were cultured in 24-well polystyrene (plastic) dishes as controls and to determine when confluence was achieved. Media were collected and cell number determined 24 h postconfluence. PGE2 and TGF-β1 levels in the conditioned media were determined using commercial radioimmunoassay and enzyme-linked immunosorbent assay kits, respectively. There was an inverse relationship between cell number and Ti surface roughness. Total PGE2 content in the media of cultures grown on the three roughest surfaces (FA, CA, and TPS) was significantly increased 1.5-4.0 times over that found in media of cultures grown on plastic or smooth surfaces. When PGE2 production was expressed per cell number, CA and TPS cultures exhibited six- to eightfold increases compared to cultures on plastic and smooth surfaces. There was a direct relationship between TGF-β1 production and surface roughness, both in terms of total TGF-β1 per culture and when normalized for cell number. TGF-β1 production on rough surfaces (CA and TPS) was three to five times higher than on plastic. These studies indicate that substrate surface roughness affects cytokine and growth factor production by MG-63 cells, suggesting that surface roughness may modulate the activity of cells interacting with an implant, and thereby affect tissue healing and implant success. © 1996 John Wiley & Sons, Inc.
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  • 3
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Surface and Interface Analysis 24 (1996), S. 204-210 
    ISSN: 0142-2421
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: Atomic force microscopy (AFM) shows that PTFE-on-silicon wafer tribological transfer films consist of narrow ribbons of PTFE, 〈1 μm wide and 〈10 nm high, aligned with the film draw direction. Within the ribbons the PTFE molecular chains are also aligned with the draw direction. Such materials are of interest as substrates for the epitaxial crystallization of polymers and small molecules. X-ray photoelectron spectroscopy demonstrates that the amount of PTFE put down increases with deposition temperature and pressure. The XPS azimuthal angle dependence at low electron take-off angle is consistent with the aligned ribbon morphology. Azimuthal and polar angle dependence and charging studies show that hydrocarbon contamination observed in the XPS spectrum is located on top of the silicon wafer substrate, in the channels between the PTFE ribbons. Imaging XPS confirms the pressure dependence of PTFE coverage, and at low deposition pressure reveals tracks of PTFE ∽100 μm wide, aligned with the film draw direction. Together with the AFM data this leads to a description of PTFE transfer films as fractal materials.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 62 (1996), S. 1819-1833 
    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: Multiblock copolymers offer the possibility to combine the properties of different polymers. Thus, new materials with tailor-made unique properties are available by coupling of different suitable polymeric segments. The goal of the work discussed in this paper was to combine advantageous properties of liquid-crystalline polymers (LCP) with those of polysulfone (PSU). Therefore, liquid crystalline poly(ethylene terephthalate-co-1,4-oxybenzoates) were connected with PSU oligomers. Chemically homogeneous multiblock copolymers with high molecular weight were obtained by a melt transesterification procedure. It was demonstrated by wide angle x-ray scattering (WAXS), polarizing microscopy, transmission electron microscopy (TEM), and differential scanning calorimetry (DSC) that the properties of the multiblock copolymers (solid phase structure, phase behavior, morphology, glass transition, and melting behavior) can be balanced by the segment length of the incorporated blocks. The investigations clearly reveal the existence of a two-phase structure. However, a change of properties compared to the corresponding homopolymers refers to certain interactions between the phase due to the chemical connection of the LCP and PSU segments. © 1996 John Wiley & Sons, Inc.
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  • 5
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Es wird über die Synthese, die Charakterisierung und die Koordinationseigenschaften der im Titel genannten Polymerliganden berichtet. Die polymeren Chelate wurden durch Polykondensation von Übergangsmetallionen (M) mit polymeren Schiffschen Basen (L) hergestellt. Die Analysenergebnisse weisen auf eine Formel (ML)n für die Chelate hin. Die Polychelate sind stabil und unlöslich in gebräuchlichen organischen Lösemitteln. Die geometrische Anordnung der Liganden um das zentrale Metallion wird auf der Basis von Messungen der magnetischen Suszeptibilitäten und UV-Reflexionsspektren beschrieben. Die Ligandenfeldaufspaltungsparameter 10 Dq, der interelektronische Abstoßungsparameter B, der nephelauxetrische Parameter β und die Ligandenfeldaufspaltungsenergien wurden für die Ni(II)- und Co(II)-Chelate berechnet. Alle Chelate sind gegenüber mäßig konzentrierten Säuren und verdiinntem Alkali bei Umgebungstemperaturen bestandig und zeigen unterschiedliche thermische Stabilität. IR-Spektren zufolge ist der Ligand in der Regel über die Carbonylsauerstoffatome (C=O) und die phenolischen OH-Gruppen unter Austausch der Wasserstoffionen durch die Metallionen koordiniert.
    Notes: The synthesis, characterization and coordination aspects of the title polymer ligands are reported. The polymeric chelates were prepared by polycondensations of transition metal ions (M) with a poly(Schiff's base) (L). The analytical data propose a (ML)n formula for the chelates. All the polychelates are stable and insoluble in common organic solvents. The geometry around the central metal ion in each chelate is proposed on the basis of measurements of magnetic susceptibilities and UV reflectance spectra. The ligand field splitting parameters 10 Dq, the interelectronic repulsion parameter B, the nephelauxetric parameter β and ligand field splitting energies (L.F.S.E.) have been calculated for Ni(II) and Co(II) chelates. All chelates are resistant to moderately concentrated acids and dilute alkalies at ambient temperature. They exhibit thermal stabilities to varying degrees. IR spectra show that the ligand usually coordinates via the carbonyl oxygen (C=O) and the phenolic OH with replacement of hydrogen by metal ions.
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  • 6
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 34 (1996), S. 649-656 
    ISSN: 0887-6266
    Keywords: liquid crystalline polymer ; quasielastic neutron scattering ; gelation ; rotational dynamics ; poly(γ-benzyl L-glutamate) ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Quasielastic neutron scattering has been used to study the motion of protons in two solutions of poly(γ-benzyl L-glutamate) (PBLG) and deuterated benzyl alcohol (DBA) as they are brought from the high temperature (cholesteric and isotropic) phase towards the gel. Quasielastic neutron scattering results demonstrate that, in both the isotropic and cholesteric phases, the local rotational dynamics of the polymer are continuous in the high temperature phases, but become more constrained as the system approaches and enters the gel phase. The results also show that the energetics of the rotational motion of the protons below the gelation threshold are independent of the initial phase and the protons are not rendered immobile in the gel phase. © 1996 John Wiley & Sons, Inc.
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  • 7
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 34 (1996), S. 1881-1891 
    ISSN: 0887-6266
    Keywords: crosslinking ; poly(p-phenylene benzobis thiazole) ; PBZT ; methyl pendant PBZT ; 13C solid state NMR ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: In order to influence the compressive strength of the rigid rod polymeric fibers, methyl pendent poly(p-phenylene benzobisthiazole) fibers have been heat treated in the 400 to 550°C temperature range in air and in nitrogen for varying times to achieve intermolecular crosslinking. These fibers have been examined using Fourier transform infrared (FTIR) spectroscopy, 13C solid-state nuclear magnetic resonance (NMR) swelling behavior, and scanning electron microscopy. 13C NMR has also been carried out on solutions of as-spun fibers. Fibers heat-treated at 400°C, both in nitrogen and in air, up to heat-treatment times of 60 min are insoluble in 99% chlorosulfonic acid, however no direct evidence of crosslinking has been obtained for these fibers using spectroscopic techniques, suggesting that in these fibers the degree of crosslinking must be very low. Evidence that methyl groups are precursors to certain crosslinks was first seen via a weak methylene resonance in 13C solid-state NMR, corresponding to about 2% of the original methyl intensity, in a sample heat-treated at 450°C in air. Fibers heat-treated in nitrogen at 550°C for 10 minutes do not exhibit any swelling in chlorosulfonic acid, are brittle, have lost most methyl groups; however, some CH2 groups form. In this fiber, the carbon intensity for the CH2 group in the 13C solid-state NMR is 18% of the intensity for the CH3 group in the as-spun fiber. The fibers heat-treated at 400 and 450°C show a fibrillar morphology, while the fibrillar morphology is not observed in the fibers heat-treated at 550°C in nitrogen for 10 min. Based on this work, it is our judgment that if heat treatment of this material is to improve compressive strength, the heat treatment protocol of time and temperature will probably be critical and the highest temperatures of exposure will probably lie in the 450 to 550°C range. © 1996 John Wiley & Sons, Inc.
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  • 8
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 34 (1996), S. 2987-2997 
    ISSN: 0887-6266
    Keywords: small molecule diffusion ; fluorescence nonradiative energy transfer ; glass transition temperature ; rubbery polymer ; probe shape effects ; probe flexibility effects ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A novel experimental approach involving fluorescence nonradiative energy transfer (NRET) is employed to study the Fickian diffusion of small molecules in rubbery poly(isobutyl methacrylate) (PiBMA) films near the glass transition, using a formalism that directly relates the small molecule translational diffusion coefficient, D, to changes in the normalized nonradiative energy transfer efficiency, EN. Values of D for pyrene, 1,3-bis-(1-pyrene) propane (BPP), 1,3-bis-(1-pyrene) decane (BPD), 9,10-bis-phenyl ethynyl anthracene (BPEA), diphenyl Disperse Red 4 (DPDR4), and decacyclene in PiBMA are measured over temperatures ranging from approximately Tg to Tg + 25°C. Among these chromophores, significant differences in both the magnitude and temperature dependence of D are observed which are attributed to differences in molecule shape and flexibility, as well as molar volume. Other factors being equal, chromophore flexibility was shown both to increase the magnitude of D and to decrease its dependence on temperature, as does an increase in aspect ratio. For BPD, these effects are attributed to the ability of the flexible molecule to diffuse in a piecewise manner, requiring the cooperative mobility of fewer polymer chain segments than a rigid molecule of the same molar volume. For BPEA and DPDR4, this deviation from D being dominated by molar volume effects is attributed the to high aspect ratio of these elongated molecules. © 1996 John Wiley & Sons, Inc.
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  • 9
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Surface and Interface Analysis 24 (1996), S. 419-421 
    ISSN: 0142-2421
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: Time-of-flight secondary ion mass spectrometry (ToF-SIMS) studies, utilizing both laterial imaging and shallow depth profiling, of a 50:50 poly(vinyl chloride)/poly(methyl methacrylate) (PVC:PMMA) blend have confirmed the presence of a thin overlayer of PMMA on the phase-separated bulk morphology.
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  • 10
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Surface and Interface Analysis 24 (1996), S. 723-728 
    ISSN: 0142-2421
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: Crystalline regions of poly(ethylene terephthalate) (PET) are associated with the trans glycol conformation of the polymer repeat unit. Amorphous regions are largely associated with the gauche conformation. We describe experiments which follow the development of trans conformers at the surface and in the bulk of amorphous PET films (∽150 nm thick) annealed above the glass transition temperature Tg. X-ray photoelectron spectroscopy was used to probe the surface region to a depth of ∽5 nm and Fourier transform infrared spectroscopy (FTIR) to examine changes in the bulk. For PET samples annealed at 90 °C no conformational change was observed either at the surface or in the bulk after 120 min. At 95 and 110 °C the gauche to trans conformational change was over in ∽30 min (surface) and 〉120 min (bulk) and ∽15 minutes (surface) and ∽30 min (bulk), respectively. Hence the surface rearranges faster than the bulk, consistent with increased mobility at the surface due to the polymer chains being less constrained. This is analogous with the phenomenon of surface premelting in crystalline solids. A comparison of reflection-absorption infrared spectroscopy and transmission FTIR data demonstrates the occurrence of molecular reorientation in the bulk in addition to conformational change.
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