scholarly journals Influence of Compression Direction on the Shape-Memory Effect of Micro-Cylinder Arrays Prepared from Semi-Crystalline Polymer Networks

MRS Advances ◽  
2016 ◽  
Vol 1 (27) ◽  
pp. 1985-1993 ◽  
Author(s):  
Yi Jiang ◽  
Liang Fang ◽  
Karl Kratz ◽  
Andreas Lendlein

ABSTRACTMicrostructured polymeric surfaces capable of a thermally-induced shape-memory effect (SME) can perform on demand changes of surface properties such as wettability or adhesion.In this study, we explored the influence of the applied compression direction during programming, i.e. vertical compression and tilted compression, on the SME of microstructured crosslinked poly[ethylene-co-(vinyl acetate)] (cPEVA) films comprising arrays of micro-cylinders with a height of 10 µm and different diameters of 10 µm, 25 µm, and 50 µm. The shape recovery of the microstructures during heating was visualized online by optical microscopy, while atomic force microscopy (AFM) was utilized to investigate the temperature-induced shape change of single micro-cylinders. Here, the changes in micro-cylinder height and the characteristic angle θ were followed and analyzed for quantification of the shape-memory performance. Both compression modes resulted in almost flat programmed surfaces as indicated by high shape fixity ratios of Rf ≥ 93±1%. A nearly complete recovery of the micro-cylinders was obtained for all investigated cPEVA samples documented by high shape recovery values of Rr ≥ 97±1%, while the obtained shape change of the micro-cylinders during recovery almost reversely recalled the applied deformation during programming. The presented capability of SMP microstructured substrates to memorize the way of deformation during programming could be a new tool for controlling particular shape changes of microstructures during recovery and in such a way the generated local recovery forces can be adjusted.

2021 ◽  
Vol 22 (11) ◽  
pp. 5892
Author(s):  
Axel T. Neffe ◽  
Candy Löwenberg ◽  
Konstanze K. Julich-Gruner ◽  
Marc Behl ◽  
Andreas Lendlein

Shape-memory hydrogels (SMH) are multifunctional, actively-moving polymers of interest in biomedicine. In loosely crosslinked polymer networks, gelatin chains may form triple helices, which can act as temporary net points in SMH, depending on the presence of salts. Here, we show programming and initiation of the shape-memory effect of such networks based on a thermomechanical process compatible with the physiological environment. The SMH were synthesized by reaction of glycidylmethacrylated gelatin with oligo(ethylene glycol) (OEG) α,ω-dithiols of varying crosslinker length and amount. Triple helicalization of gelatin chains is shown directly by wide-angle X-ray scattering and indirectly via the mechanical behavior at different temperatures. The ability to form triple helices increased with the molar mass of the crosslinker. Hydrogels had storage moduli of 0.27–23 kPa and Young’s moduli of 215–360 kPa at 4 °C. The hydrogels were hydrolytically degradable, with full degradation to water-soluble products within one week at 37 °C and pH = 7.4. A thermally-induced shape-memory effect is demonstrated in bending as well as in compression tests, in which shape recovery with excellent shape-recovery rates Rr close to 100% were observed. In the future, the material presented here could be applied, e.g., as self-anchoring devices mechanically resembling the extracellular matrix.


2008 ◽  
Vol 47-50 ◽  
pp. 690-693 ◽  
Author(s):  
Da Wei Zhang ◽  
Jin Song Leng ◽  
Yan Ju Liu

This paper is concerned about the synthesis of shape memory styrene copolymer and the investigation of the influence of radialization dosage on its shape memory effect. As one of novel actuators in smart materials, shape memory polymers (SMPs) have been investigated intensively. Styrene copolymer with proper cross-linking degree can exhibit shape memory effect (SME). In this paper, the influence of radialization on shape memory effect of styrene copolymer was investigated through altering the dosage of radialization. The radialization dosage of styrene copolymer was determined by changed radicalization time. The glass transition temperature (Tg) of styrene copolymerwas measured by Dynamic Mechanical Analysis (DMA). The shape memory performance of styrene copolymer with different radiated dosage was also evaluated. Results indicated that the shape memory polymer (SMP) was synthesized successfully. The Tg increased from 60°C to 65°C followed by increasing the radialization dosage. Moreover, the SMP experienced good SME and the largest reversible strain of the SMP reached as high as 150%. When heating above Tg+30°C (different copolymers performed different Tg), the shape recovery speed of the copolymers increased with increasing the radialization dosage. However, the recovery speed decreased with increasing the radialization dosage at the same temperature of 95°C.


Author(s):  
Axel T. Neffe ◽  
Candy Löwenberg ◽  
Konstanze K. Julich-Gruner ◽  
Marc Behl ◽  
Andreas Lendlein

Shape-memory hydrogels (SMH) are as multifunctional, actively-moving polymers of interest in biomedicine. In loosely crosslinked polymer networks gelatin chains may form triple helices, which can act as temporary netpoints in SMH, depending on the presence of salts. Here, we show programming and initiation of the shape-memory effect of such networks based on a thermomechanical process compatible with the physiological environment. The SMH were synthesized by reaction of glycidylmethacrylated gelatin with OEG α,ω-dithiols of varying crosslinker length and amount. Triple helicalization of gelatin chains is shown directly by wide-angle X-ray scattering and indirectly via the mechanical behavior at different temperatures. The ability to form triple helices increased with the molar mass of the crosslinker. Hydrogels had storage moduli of 0.27-23 kPa and Young’s moduli of 215-360 kPa at 4 °C. The hydrogels were hydrolytically degradable, with full degradation to water soluble products within one week at 37 °C and pH = 7.4. A thermally-induced shape-memory effect is demonstrated in bending as well as in compression tests, in which shape recovery with excellent shape recovery rates Rr close to 100% were observed. In the future, the material presented here could be applied e.g. as self-anchoring devices mechanically resembling the extracellular matrix.


2014 ◽  
Vol 936 ◽  
pp. 140-144 ◽  
Author(s):  
Jia Ying ◽  
Masaaki Nishikawa ◽  
Masaki Hojo

The relationship of annealing and shape memory effect of uniaxially oriented shape memory polyurethane was studied; meanwhile a new method of adjusting shape recovery ratio by annealing was proposed for further consideration. Experiments were designed to compare the influence on length change from annealing and shape memory effect with shape memory polyurethane film at 65°C. We found that for shape memory polyurethane which had residual strain from material processing procedure, annealing and shape memory effect have the same effect on its length change if they are both carried out at the same temperature. It is because annealing and shape memory effect have the same mechanism, which is the change of state from low conformational entropy states to the recovery of a stable high entropy state in the polymer. Moreover, it is proved by experiment that shape recovery ratio of shape memory polyurethane can be adjusted by annealing.


2004 ◽  
Vol 449-452 ◽  
pp. 1273-1276 ◽  
Author(s):  
Masahiko Ikeda ◽  
S. Komatsu ◽  
Yuichiro Nakamura ◽  
Y. Kobayashi

Using Ti-40mass%Ta-0, -4, -8 and -12mass%Sn alloys, the effect of Sn addition on phase constitution in the solution treated and quenched state and isochronal heat treatment behavior is studied by electrical resistivity and Vickers hardness measurements and X-ray diffactometry. To confirm shape memory effect of some of these alloys, shape-recovery test was also performed. Orthorhombic martensite, ” was identified in Ti-40Sn-0 to 8Sn alloy quenched from 1173K, while phase was identified in STQed Ti-40Ta-12Sn alloy. On isochronal heat treatment, increases of resistivity at LN and resistivity ratio were observed in only 8Sn alloy, because these increases are due to reverse-transformation of ” to phase. From result of shape recovery test, shape memory effect was observed in Ti-40Ta-4 and 8Sn alloys


2010 ◽  
Vol 654-656 ◽  
pp. 2150-2153 ◽  
Author(s):  
Hideki Hosoda ◽  
Makoto Taniguchi ◽  
Tomonari Inamura ◽  
Hiroyasu Kanetaka ◽  
Shuichi Miyazaki

Effects of single- and multi-step aging on mechanical properties and shape memory properties of Ti-6Mo-8Al (mol%) biomedical shape memory alloy were studied using tensile tests at room temperature (RT). The solution-treated alloy at RT was two phase of bcc β and martensite α". Tensile tests revealed that the solution-treated alloy exhibited good shape memory effect. As for the single-step aging, (1) pseudoelastic shape recovery by unloading was observed after aging at 623K, (2) the alloy became brittle after aging at 773K due to ω embrittlement, and (3) strength was improved with small shape memory effect by aging at 1023K. On the other hand, after a multistep aging at 773K-1023K-1123K, the alloy was strengthened and showed perfect shape recovery. The improvement must be achieved by the formation of fine and uniform hcp α precipitates.


2005 ◽  
Vol 475-479 ◽  
pp. 2399-2402 ◽  
Author(s):  
Xili Lu ◽  
Wei Cai ◽  
Lian Cheng Zhao

Poly(L-lactide) (PLLA) was synthesized by the ring-opening polymerization of L-lactide and the shape memory behavior was studied using DSC and bending test experiments. The results indicate that the specimen shows the shape memory effect (SME), the small crystalline phase of PLLA and the mobility of amorphous phase may be responsible for the SME. The shape recovery of samples decreases and approaches to steady with the testing number increases.


1983 ◽  
Vol 21 ◽  
Author(s):  
C. M. Wayman

ABSTRACTInvestigations of the shape memory effect in alloys forming thermoelastic martensites with various crystal structures (2H, 3R, 9R and 18R) reveal that universal behavior exists. A unified explanation of the martensite deformation processes and subsequent shape recovery is now in hand, even though the various martensites are both internally twinned and internally faulted and, in addition, have different crystal structures. In cases studied to date, an initial parent phase single crystal transforms into self-accommodating arrangements of martensite variants (plates) which are characterized by “plate groups.” Each group consists of four variants. The average shape deformation in a plate group is essentially zero.Upon stressing below the Mf temperature the martensite undergoes deformation by detwinning (2H and 3R only), variant-variant coalescence and twinning processes, and further group-to-group coalescence. The deformed specimen eventually becomes a single crystal of martensite consisting of that particular habit plane variant whose shape deformation permits maximum extension in the direction of the applied stress. The deformed martensite persists after unloading has occurred; reverse rearrangements of twins and variants do not occur. Specimens deformed below Mf regain their initial shape characteristic of the initial parent phase upon heating from As to Af, during which the single crystal of martensite obtained by stressing the 24-variant configuration transforms back to the original parent phase single crystal in a unique manner, which is basically a simple “unshearing” process. The unshearing is the essence of the memory.The two-way shape memory effect results after the initial martensitic transformation upon cooling is preprogrammed by the introduction of stresses which preferentially bias the transformation so that only a single variant of martensite forms upon cooling. The shape change of this single variant causes the characteristic spontaneous “bending” upon cooling. The characteristic “unbending upon heating is as with the conventional “one-way” shape memory effect.


2021 ◽  
Vol 7 (2) ◽  
pp. 2-10
Author(s):  
Alexander Shelyakov ◽  
Nikolay Sitnikov ◽  
Irina Khabibullina ◽  
Kirill Borodako ◽  
Oleg Sevryukov

Rapidly quenched quasibinary TiNi–TiCu system alloys with high copper contents (above 20 at.%) exhibit excellent shape memory effect and have considerably narrower hysteresis as compared with the TiNi binary alloy, this advantage being of special importance for cyclic load applications, e.g. for microelectromechanics (MEMS). The aim of this work is to study the effect of annealing parameters and copper content on the shape memory effect in TiNiCu alloys. Thin amorphous ribbons of TiNi-TiCu alloys with copper contents of 25 to 40 at.% were produced by planar flow casting at a melt cooling rate of about 106 K/s. The alloys were crystallized by isothermal annealing with variable duration and by exposing specimens to a short (10 ms) electric pulse. Increasing the copper content to above 30 at.% considerably reduces the plasticity and shape memory effect of the alloys. However, significant reduction of annealing duration greatly improves the shape memory performance due to prevention of the formation of brittle Ti-Cu phases in the alloys structure.


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