ALBERT

All Library Books, journals and Electronic Records Telegrafenberg

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 34 (1996), S. 157-163 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: From data in the literature on relative rates of copolymerization it has been possible to evaluate two constants, Q and e, characteristic of an individual monomer, which appear to account satisfactorily for its behavior in copolymerization. The constant Q describes the “general monomer reactivity” and is apparently related to possibilities for stabilization in a radical adduct. The constant e takes account of polar factors influencing copolymerization.
    Additional Material: 5 Tab.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 27 (1989), S. 253-258 
    ISSN: 0887-6258
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 3
    ISSN: 1045-4861
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: Bone-implant displacements can be caused by rigid body motion and by differences in material properties of the implant and bone. In the present study of the tibial component in total knee replacement, we tested a series of tibial component fixation designs to determine how certain design features influenced the magnitude of the tangential displacement between the component and supporting bone in a canine model. The transverse expansion of the proximal tibia under static axial loading was measured in the intact tibia and then in the same bone following implantation of tibial components with different interface characteristics: cementless flat smooth, cementless flat porous-coated, cementless flat porous-coated with screws, cementless pegged porous-coated, cementless pegged porous-coated with screws, cemented pegged, and cemented pegged with screws. In all cases, the magnitude of the transverse expansion increased with higher applied loads. When the statistical analysis was restricted to the cementless interfaces, the presence/absence of the porous coating, the presence/absence of pegs, and the use of screws had no significant influence on tibial expansion. However, in an analysis including the cemented and cementless pegged components, tibial expansion was reduced with the use of screws. The magnitude of the interface motion due to these displacement incompatibilities was approximately fivefold lower than the amount of interface motion related to rigid body motion found in a separate study with the canine model. The measured expansion was similar in the intact tibiae and the implanted tibiae, suggesting that the transverse constraint in the canine proximal tibia must be provided by the surrounding cortical ring rather than the subchondral bone. © 1994 John Wiley & Sons, Inc.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 43 (1991), S. 801-815 
    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 ambient temperature structure-property orientation behavior in two different polyureaurethane polymers (one cross-linked and one linear) was measured by using infrared dichroism along with mechanical response. Thin films (plaques) thermally compression-molded from TDI-polypropylene (PO) flexible water-blown polyurea-urethane foams and solution-cast TDI-PO polyurea-urethane elastomers were studied. Segmental orientation was measured as a function of elongation and relaxation, as well as of hysteresis behavior. The level of strain was 50-70% for the plaques and up to 240% for the elastomer. The soft segments for both materials exhibited a low state of orientation with elongation. Small changes in orientation with time and upon cyclic straining were also observed for the soft segments. Significant transverse orientation upon stretching was observed in the hard segments of the plaques and up to elongations of 100% for the elastomer. The transverse behavior of the hard segments in the plaques pressed from the foams was attributed to both the smaller hard domains as well as to the polyurea aggregates that have been reported to be present in flexible foams. This transverse behavior also suggested that the smaller hard domains and the polyurea aggregates possess a lamellarlike structure. At low strain levels (up to 50%), only small amounts of orientation hysteresis as well as mechanical hysteresis were observed for the hard segments of the plaques as well as for the elastomer. No significant relaxation in orientation was detected for the hard segments of both materials at a 30% strain level.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 50 (1993), S. 293-301 
    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: Samples of flexible water-blown slabstock polyurethane foams were compressed under constant load to study the effects of cycling moisture content on creep behavior and compare this behavior with the creep response where either a constant high or low moisture environment existed at the same temperature. Three sets of foams were tested: (1) 4 pph water content slabstock foam; (2) 5 pph water content slabstock foam; and (3) 2 pph water content molded foam. As the moisture conditions were cycled from low to high humidity while maintaining constant temperature in an environmental chamber, the compressive strain increased in subsequent steps with larger increases observed during the desorption portion of the humidity cycling. All three sets of foams showed similar behavior at a given temperature. At a temperature of 40°C, the strain levels under cyclic moisture conditions surpassed those levels observed at the highest constant relative humidity. During the first absorption step, the creep level increased. During any subsequent absorption step, the creep level either increased very little or none at all. Finally, during any desorption step, the creep level increased. This overall phenomenon of enhanced creep under cyclic moisture levels is attributed to water interacting with the hydrogen bonded structure within the foam. These hydrophillic interactions, principally promoted within the hard segment regions due to high hydrogen bonding, are disrupted causing slippage and increased in strain. As the foam is rapidly dired, regions of free volume are induced by the loss of water thus causing further increases in strain Prior to the reestablishment of well ordered hydrogen bonding. Further support to this proposition was given by the results obtained at a temperature of 90° C where it is well known that hydrogen bonds are much more mobile. Here, the strain levels under cyclic moisture conditions were nearly the same as those under constant high relative humidity. Weakening of the hydrogen bonds by means such as increased temperature resulted in similar strain levels to those under cyclic moisture levels. © 1993 John Wiley & Sons, Inc.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 52 (1994), S. 569-576 
    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 compression creep behavior was monitored at constant temperature and/or relative humidity for two slabstock foams with different hard-segment content. The tests were performed by applying a constant load (free falling weight) and then monitoring the strain as a function of time over a 3-h time period. A near linear relationship is obtained for linear strain versus log time after a short induction period for both foams and at most conditions studied (except at temperatures near and above 125°C). The slope of this relationship or the initial creep rate is dependent on the initial strain level, espcially in the range of 10-60% deformation. This dependence is believed to be related to the cellular structs buckling within this range of strain. At deformations greater than 60% and less than 10%, the solid portion of the foam is thought to control the compressive creep behavior in contrast to the cellular texture. Increasing relative humidity does cause a greater amount of creep to occur and is believed to be a result of water acting as a plasticizer. For low humidities increasing the temperature from 30 to 85°C, a decrease in the rate of creep is observed at a 65% initial deformation. At 125°C, an increase in the creep rate is seen and is believed to be related to chemical as well as additional structural changes taking place in the solid portion of the foams. The creep rate is higher for the higher hard-segment foam (34 wt %) than that of the lower (21 wt %) at all of the conditions studied and for the same initial deformation level. This difference is principally attributed to the greater amount of hydrogen bonds available for disruption in the higher hard-segment foam. © 1994 John Wiley & Sons, Inc.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 52 (1994), S. 1459-1476 
    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: Characterization of a series of flexible polyurethane foams that contain LiCl in their formulation is discussed. These foams were developed in order to provide an alternative method to produce foams without physical blowing agents and still attempt to maintain specific important physical properties. Three high water content foams of varying LiCl content have been characterized by utilizing several morphological techniques as well as by their viscoelastic behavior. From a morphological standpoint, it appears that by adding LiCl to the formulation, there is less formation of urea-rich aggregates that occur when LiCl is absent. Also, the hard segments are more dispersed as single units within the network. The cellular texture of the LiCl-containing foams also shows a greater amount of cellular window material than the same foam without LiCl. Both of these changes due to LiCl addition are believed to bring about a significant increase in the amount of viscoelastic decay. This decay has been observed in tensile stress relaxation, compression load relaxation, and compressive creep studies. Temperature also has a more significant effect on the compression load relaxation behavior of foams with LiCl in their formulation than when absent. These differences in viscoelastic behavior between foams with and without LiCl in their formulation are attributed to the greater mobility of the hard segments in the presence of the LiCl additive serving as a localized “hard segment” plasticizer that also promotes more phase mixing in the foams. © 1994 John Wiley & Sons, Inc.
    Additional Material: 17 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 17 (1973), S. 1631-1633 
    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: 1 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 45 (1992), S. 1983-1994 
    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: Wholly aromatic polyamides, including poly(1,4-phenyleneisophthalamide) and poly(1,4-phenyleneterephthalamide) are N-methylated to render them soluble in N,N-dimethylformamide, a common size-exclusion chromatography eluent. The procedure N-methylates 50-55% of the total amide linkages in these two examples, permitting reproducible measurement of their absolute molecular weight distributions using differential viscometry detection. There is no observable degradation in molecular weight resulting from the N-methylation, provided the excess methylating reagent is destroyed shortly after completion of the derivatization by quenching with potassium acetate. The validity of the molecular weight data obtained by the method is confirmed by light-scattering measurements on derivatized polymer and by comparison to the molecular weight of underivatized polymer that can be approximated from the intrinsic viscosity in concentrated sulfuric acid. The method is applicable to a variety of wholly aromatic polyamide structures. Examples are given.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 35 (1988), S. 601-629 
    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: A series of four TDI-polypropylene oxide (PO) water-blown flexible polyurethane foams was produced in which the water content was varied from 2 to 5 pph at a constant isocyanate index of 110. A portion of each foam was thermally compression molded into a plaque. The morphology of both the foams and plaques was investigated using dynamic mechanical spectroscopy (DMS), differential scanning calorimetry (DSC), transmission electron microscopy (TEM), scanning electron microscopy (SEM), swelling, wide angle X-ray scattering (WAXS), and small angle X-ray scattering (SAXS). A high degree of microphase separation occurs in these foams, and its degree is nearly independent of water (hard segment) content. In the foam with the lowest water content the morphology possesses many similarities to that of typical linear segmented urethane elastomers. Small hard segment domains are present with a correlation distance of about 7.0 nm. When the water content is increased a binodal distribution of hard segment material appears. There are the small hard segment domains typical of segmented urethane elastomers as well as larger “hard aggregates” greater than 100 nm in size. The larger domains are thought to be aggregates of rich polyurea that develop by precipitation during the foaming reaction. WAXS patterns of the foams suggest urea and possibly hard segment ordering that may be of a paracrystalline nature but certainly lacking in true 3-dimensional crystallinity.
    Additional Material: 15 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...