Memory Polymer (memory + polymer)

Distribution by Scientific Domains
Distribution within Polymers and Materials Science

Kinds of Memory Polymer

  • shape memory polymer


  • Selected Abstracts


    Modeling the Relaxation Mechanisms of Amorphous Shape Memory Polymers

    ADVANCED MATERIALS, Issue 31 2010
    Thao. D. Nguyen
    Abstract In this progress report, we review two common approaches to constitutive modeling of thermally activated shape memory polymers, then focus on a recent thermoviscoelastic model that incorporates the time-dependent effects of structural and stress relaxation mechanisms of amorphous networks. An extension of the model is presented that incorporates the effects of multiple discrete structural and stress relaxation processes to more accurately describe the time-dependent behavior. In addition, a procedure is developed to determine the model parameters from standard thermomechanical experiments. The thermoviscoelastic model was applied to simulate the unconstrained recovery response of a family of (meth)acrylate-based networks with different weight fractions of the crosslinking agent. Results showed significant improvement in predicting the temperature-dependent strain recovery response. [source]


    Tunable Nanowrinkles on Shape Memory Polymer Sheets

    ADVANCED MATERIALS, Issue 44 2009
    Chi-Cheng Fu
    Controllable biaxial and uniaxial nanowrinkles (see figure) are fabricated by a simple two-step approach , metal deposition and subsequent heating , based on shape memory polymer (prestressed polystyrene) sheets. The wavelengths of the wrinkles can be tuned by controlling the thickness of deposited metal. The ready integration of the nanowrinkles into microchannels and their effectiveness in surface enhanced sensing is demonstrated. [source]


    Melt spun thermoresponsive shape memory fibers based on polyurethanes: Effect of drawing and heat-setting on fiber morphology and properties

    JOURNAL OF APPLIED POLYMER SCIENCE, Issue 4 2007
    Jasmeet Kaursoin
    Abstract Thermoresponsive shape memory (SMP) fibers were prepared by melt spinning from a polyester polyol-based polyurethane shape memory polymer (SMP) and were subjected to different postspinning operations to modify their structure. The effect of drawing and heat-setting operations on the shape memory behavior, mechanical properties, and structure of the fibers was studied. In contrast to the as-spun fibers, which were found to show low stress built up on straining to temporary shape and incomplete recovery to the permanent shape, the drawn and heat-set fibers showed significantly higher stresses and complete recovery. The fibers drawn at a DR of 3.0 and heat-set at 100°C gave stress values that were about 10 times higher than the as-spun fibers at the same strain and showed complete recovery on repeated cycling. This improvement was likely due to the transformation brought about in the morphology of the permanent shape of the SMP fibers from randomly oriented weakly linked regions of hard and soft segments to the well-segregated, oriented and strongly H-bonded regions of hard-segments. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 2172,2182, 2007 [source]


    Shape Memory Effect of Bacterial Poly[(3-hydroxybutyrate)- co -(3-hydroxyvalerate)],

    MACROMOLECULAR RAPID COMMUNICATIONS, Issue 13 2005
    Young Baek Kim
    Abstract Summary: A bacterial poly[(3-hydroxybutyrate)- co -(3-hydroxyvalerate)] biosynthesized by Pseudomonas sp. HJ-2 was found to be a shape memory polymer. Permanent shapes were set by annealing at room temperature the samples that had been pre-treated above 95,°C in specified shapes. The temporary shapes were set by stretching and holding the elongated samples. Thermal shrinkage began at 45,°C and stopped at 75,°C to recover to their permanent shapes. Apparently, the orientation induced the formation of hard segments that were responsible for setting the temporary shapes. The shape memory effect of this polymer was explained based on the DSC and XRD results at different phases. The recovery of a coil shape upon heating a strip of HJ-2 PHB35V, demonstrating the polymers shape memory effect. [source]


    Thermomechanical studies of aluminum nitride filled shape memory polymer composites

    POLYMER COMPOSITES, Issue 3 2007
    Muhammad Yasar Razzaq
    High thermal conductivity polyurethane shape memory polymer (SMP) composites filled with aluminum nitride (AlN) were fabricated, and their thermal and thermomechanical properties were studied. The purpose of this microstructure is to improve the thermal properties of the SMPs at low filler content. Morphology of AlN filler in polyurethane SMP matrix and the resulting thermal conductivity was also investigated. Thermal studies have shown that AlN is an effective filler for reinforcement of the polyurethane SMP and that it does not deteriorate the stable physical crosslink structure of the polyurethane, which is necessary to store the elastic energy in the service process of the shape memory material. The thermal conductivities of these SMP composites in relation to filler concentration and temperature were investigated, and it was found that the thermal conductivity can increase up to 50 times in comparison with that of the pure SMP. Furthermore, differential scanning calorimetry tests have shown a significant decrease in the glass transition temperature of the switching segment. Dynamic mechanical studies have shown that the storage modulus of the composites increase with higher AlN content in both glassy and rubbery state. Damping peak decreases and also the curve of damping becomes broader with increasing filler content. Strain fixity rate which expresses the ability of the specimens to fix their strain has been improved slightly in the presence of AlN filler but the final recovery rate of the shape memory measurement has decreased evidently. POLYM. COMPOS., 28:287,293, 2007. © 2007 Society of Plastics Engineers [source]


    Triple-Shape Polymeric Composites (TSPCs)

    ADVANCED FUNCTIONAL MATERIALS, Issue 16 2010
    Xiaofan Luo
    Abstract In this paper, the fabrication and characterization of triple-shape polymeric composites (TSPCs) that, unlike traditional shape memory polymers (SMPs), are capable of fixing two temporary shapes and recovering sequentially from the first temporary shape (shape 1) to the second temporary shape (shape 2), and eventually to the permanent shape (shape 3) upon heating, are reported. This is technically achieved by incorporating non-woven thermoplastic fibers (average diameter ,760 nm) of a low- Tm semicrystalline polymer into a Tg -based SMP matrix. The resulting composites display two well-separated transitions, one from the glass transition of the matrix and the other from the melting of the fibers, which are subsequently used for the fixing/recovery of two temporary shapes. Three thermomechanical programming processes with different shape fixing protocols are proposed and explored. The intrinsic versatility of this composite approach enables an unprecedented large degree of design flexibility for functional triple-shape polymers and systems. [source]


    Modeling the Relaxation Mechanisms of Amorphous Shape Memory Polymers

    ADVANCED MATERIALS, Issue 31 2010
    Thao. D. Nguyen
    Abstract In this progress report, we review two common approaches to constitutive modeling of thermally activated shape memory polymers, then focus on a recent thermoviscoelastic model that incorporates the time-dependent effects of structural and stress relaxation mechanisms of amorphous networks. An extension of the model is presented that incorporates the effects of multiple discrete structural and stress relaxation processes to more accurately describe the time-dependent behavior. In addition, a procedure is developed to determine the model parameters from standard thermomechanical experiments. The thermoviscoelastic model was applied to simulate the unconstrained recovery response of a family of (meth)acrylate-based networks with different weight fractions of the crosslinking agent. Results showed significant improvement in predicting the temperature-dependent strain recovery response. [source]