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  • 1
    Digitale Medien
    Digitale Medien
    s.l. : American Chemical Society
    Macromolecules 12 (1979), S. 479-483 
    ISSN: 1520-5835
    Quelle: ACS Legacy Archives
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    s.l. : American Chemical Society
    Macromolecules 19 (1986), S. 828-833 
    ISSN: 1520-5835
    Quelle: ACS Legacy Archives
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    Oxford UK : Blackwell Science Ltd
    Journal of oral rehabilitation 28 (2001), S. 0 
    ISSN: 1365-2842
    Quelle: Blackwell Publishing Journal Backfiles 1879-2005
    Thema: Medizin
    Notizen: Dielectric characterization evaluated the influence of sorbed moisture on urethane dimethacrylate (UDMA) polymer matrix and unsilanated and silanated zirconia-silica (ZS)-filled UDMA composites. The moisture content (MC) of samples tested ranged from 0 to 7·32% with maximum values for UDMA, silanated and unsilanated ZS-filled UDMA were 3·72, 6·0 and 7·32%, respectively. Dielectric spectra were measured from 0·053 to 100 kHz and from −180 to 180 ¯C. Small MC stiffened the polymers, which was shown by a shift of β-peaks to higher temperatures, a decrease in the half width of bands and an increase in the change of activation energies. Higher MC resulted in water plasticizing the polymer by shifting the β-peaks to lower temperatures. Maximum water sorption restricted the motion of the polymer chains and the b-peaks shifted to higher temperatures. Further, increasing MC shifted the a-relaxation to lower temperatures in both UDMA and composites. However, in composites with unsilanated ZS, a new relaxation occurred at high temperatures and low frequencies which was attributed to Maxwell–Wagner–Sillars (MWS) polarization. Thus, in UDMA, water occurs as fragments that form non-freezing clusters. However, in unsilanated ZS–UDMA composites, bulk water can exist at the polymer–filler interface and form disordered structures of ice at low temperatures which can evaporate at high temperatures. Silanated ZS–UDMA composites function similarly to UDMA at low MC but are more plasticized at high temperatures.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 4
    Digitale Medien
    Digitale Medien
    Oxford, UK : Blackwell Science Ltd
    Journal of oral rehabilitation 27 (2000), S. 0 
    ISSN: 1365-2842
    Quelle: Blackwell Publishing Journal Backfiles 1879-2005
    Thema: Medizin
    Notizen: The polymer–filler interaction of a dental composite was examined by dielectric measurements to determine how a non-compatible inorganic phase modifies the molecular behaviour of the polymer chains and how modification of this phase by silanation can affect these molecular behaviours. Urethane dimethacrylate (UDMA) monomer and zirconia–silica (ZS) powder were used as organic and inorganic phases, respectively. 3-Acryloxypropyltrimethoxysilane (MAPM) and 4-aminobutyltriethoxysilane (ABTE) were used as silanating coupling agents. The components of the composite were mixed in different ratios after treating the filler with from 0 to 30 times the minimum uniform coverage with the silane, then the composite was made into thin films. The dielectric spectra of five replicas for each filler–monomer ratio were measured, and three replicas were measured for each silane and for each amount of silane used to treat the filler. Increasing the filler concentration in the composites decreased the intensity of Tan(Δ) for the α- and β-relaxations, where the β-relaxations also became broader and the α-relaxations were totally obstructed. The α-relaxations were shifted to higher temperatures, while the β-relaxations were shifted to lower temperatures. Filler treatment with small amounts of MAPM shifted the α-relaxations to higher temperatures; they were shifted back to lower temperatures when the filler was treated with large amounts of silane. Filler treatment with large amounts of ABTE (30-fold) caused an extra peak to emerge in the high-temperature region. It can be concluded that increasing filler concentration restricts the mobility of the main chains and decreases the thickness of the surface layer, while allowing more movement of the local chains. Filler treatment with MAPM was shown to be a compatible coupling agent with the ZS and the UDMA systems. Such compatibility was observed through the effectiveness of the chemical linkage of the silane to the filler and the polymer without forming a separate inter-phase. Filler treatment with ABTE was shown to be an incompatible coupling agent for the ZS-filled UDMA system. The incompatibility was observed by the occurrence of a new peak that characterizes an inter-phase.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 5
    Digitale Medien
    Digitale Medien
    Springer
    Colloid & polymer science 255 (1977), S. 714-714 
    ISSN: 1435-1536
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie , Maschinenbau
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 6
    Digitale Medien
    Digitale Medien
    Springer
    Journal of materials science 27 (1992), S. 990-1000 
    ISSN: 1573-4803
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Maschinenbau
    Notizen: Abstract The “basic longitudinal texture”, which is present everywhere on the fracture surfaces of glassy thermosets and is the finest texture observed on such surfaces, consists of low ridges and shallow grooves that are aligned parallel with the direction of crack propagation. The periodicity of the basic longitudinal texture, i.e., the average lateral separation between the ridges (or grooves), has been found to be characteristic of materials. This and other properties were measured for a series of rigid epoxy specimens made from diglycidyl ether of bisphenol-A and methylhexahydrophthalic anhydride. For the series of epoxies studied, the glass transition temperatures varied from 76 to 143 °C, the room temperature Young's modulus varied from 2.29 to 2.97 G Pa, the room temperature yield stress in compression varied from 99 to 128 M Pa, the room temperature Knoop hardness numbers varied from 133.5 to 163.5, the rubbery modulus at 200'C varied from 12.8 to 21.6 MPa, and the periodicity of the basic longitudinal texture varied from 205 to 368 nm. Only properties of the liquid state, namely glass transition temperature and the rubbery modulus, correlated well with periodicity of the basic longitudinal texture. This suggests that the basic longitudinal texture is the remnant left on the fracture surfaces of a liquid state that must have developed during fracture. This suggests in turn that liquefaction is an intrinsic part of the brittle fracture of polymer network glasses.
    Materialart: Digitale Medien
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  • 7
    Digitale Medien
    Digitale Medien
    Springer
    Journal of materials science 22 (1987), S. 1934-1940 
    ISSN: 1573-4803
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Maschinenbau
    Notizen: Abstract The temperature changes as a result of rapid hydrostatic pressure applications are reported for high density polyethylene (HDPE) and low density polyethylene (LDPE) in the reference temperature range from 298 to 423 K and in the pressure range from 13.8 to 200 MN m−2. The adiabatic temperature changes were found to be a function of pressure and temperature. A curve fitting analysis showed that the empirical curve (∂/∂P) =ab(ΔP)b−1 described the experimental thermoelastic coefficients obtained from the experiments. The data were analyzed by determining the predicted thermoelastic coefficients derived from the Thomson equation (∂/∂P)θ = αT 0/ϱC p. The experimental and predicted Grüneisen parameter γ T were also determined.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 8
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 14 (1974), S. 352-356 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: The effect of insoluble gel material, crystalline aggregates, and suspension particle membranes on the physical and mechanical properties of solution cast films of suspension PVC has been studied. The chemical structure and morphology of the insoluble gel material was also studied. The suspension particle membranes are found to contain significant amounts of hydroxyl and carbonyl groups but are still predominately PVC. These particles affect the transparency of cast films as well as the surface topography by forming discrete clusters upon drying which are uniformly distributed throughout the films. Finally, insoluble gel material is found to have no significant effect on the low and high speed mechanical properties of the films.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 9
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 26 (1986), S. 1060-1065 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: The adiabatic temperature changes for poly(methyl methacrylate) (PMMA) and high-density polyethylene are reported as the result of rapid compressive stress applications at different temperatures. A specially-modified Instron capillary rheometer was used in the experiments. Results were examined by determining the experimental thermoelastic coefficients (δT/δ). These were compared with the predicted coefficients from the equation (δT/δ) = ∝LTo/ρCp. Good agreement was found for ambient temperature, and deviations were found for higher temperatures. High-density polyethylene showed higher temperature changes than PMMA, the causes for which are also discussed.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 10
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 33 (1987), S. 2151-2163 
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: The temperature changes as a result of rapid hydrostatic pressure applications are reported for poly(hexamethylene adipamide) (nylon 66) and poly(oxymethylene) (POM) in the reference temperature range from 298 to 423 K and in the pressure range from 13.8 to 200 MN/m2. The adiabatic temperature changes were found to be a function of pressure and temperature. A curve fitting analysis showed that the empirical curve (∂T/∂P) = ab(ΔP)b-1 described the experimental thermoelastic coefficients obtained from the experiments. The data were analyzed by determining the predicted thermoelastic coefficients derived from the Thomson equation (∂T/∂P) = αT0/ρCp. The experimental and predicted Grüneisen parameter γT were also determined. The relationship between the thermal effects and the chain molecular motion is discussed by including dynamic mechanical analysis and DSC measurements for the nylon 66 and POM samples.
    Zusätzliches Material: 8 Ill.
    Materialart: Digitale Medien
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