The thermally induced unidirectional shape-shape-memory effect is an effect classified within the new so-called smart materials. Polymers with thermally induced shape-memory effect are new materials, whose applications are recently being studied in different fields of science (e.g., medicine), communications and entertainment.
There are currently reported and commercially used systems. However, the possibility of programming other polymers is present, due to the number of copolymers that can be designed: the possibilities are almost endless.
See also: Shape-memory polymer. Polymers with thermally induced shape-memory effect are those polymers that respond to external stimuli and because of this have the ability to change their shape. The thermally induced shape-memory effect results from a combination of proper processing and programming of the system.
This effect can be observed in polymers with very different chemical composition, which opens a great possibility of applications.
In the first step the polymers are processed by means of common techniques, such as injection or extrusion, thermoforming, at a temperature (THigh) at which the polymer melts, obtaining a final shape which is called "permanent" shape.
The next step is called system programming and involves heating the sample to a transition temperature (TTrans). At that temperature the polymer is deformed, reaching a shape called "temporary". Immediately afterwards the temperature of the sample is lowered.
The final step of the effect involves the recovery of the permanent shape. The sample is heated to the transition temperature (TTrans) and within a short time the recovery of the permanent shape is observed.
This effect is not a natural property of the polymer, but results from proper programming of the system with the appropriate chemistry.
For a polymer to exhibit this effect, it must have two components at the molecular level: bonds (chemical or physical) to determine the permanent shape and "trigger" segments with a TTrans to fix the temporary shape.
It should first be noted that the first inelastic mechanism of these polymers is the mobility of the chains and the conformational rearrangement of the groups. Then the effect on semi-crystalline and amorphous polymers must be distinguished. In both cases, anchor points must be created that act as "triggers" for the effect. In the case of amorphous polymers, these will be the knots or "tangles" of the chains, and in the case of semi-crystalline polymers, the crystals themselves will form these anchor points.
By modifying the shape of the material under minimal critical stress, the chains slide and a metastable structure is created, which increases the organization and order of the chains (lower entropy), when the deformation load is eliminated, the anchor points provide a storage mechanism for macroscopic stresses in the form of small localized stresses and decreasing entropy.
In the glassy state the rotational motions of the molecules are frozen and impeded, as the temperature increases and the glassy state is reached, these motions thaw and rotations and relaxations occur, the molecules take the form that is entropically most favorable to them, the one with the lowest energy. These movements are called relaxation process and the formation of "random strings" to eliminate stresses is called shape-memory loss.
A polymer will exhibit the shape-memory effect if it is susceptible to being stabilized in a given state of deformation, preventing the molecules from slipping and regaining their higher entropy (lower energy) form. This can be achieved almost entirely by creating crosslinking or vulcanization, these new bonds act as anchors and prevent the relaxation of the chains, the anchor points can be physical or chemical.
The unidirectional shape-shape-memory effect was first observed by Chand and Read in 1951 in a Gold-Cadmium alloy and in 1963 Buehler described this effect for nitinol, which is an equiatomic Nickel-Titanium alloy.
This effect in metals and ceramics is based on a change in the crystal structure, called martensitic phase transition. The disadvantage of these materials is that it is an equiatomic alloy and deviations of 1% in the composition modify the transition temperature by approximately 100 K.
Some metals and ceramics present the effect bidirectionally, which means that at a certain temperature there is a shape and this can be changed by changing the temperature, but if the first temperature is recovered, also the first shape is recovered. This is achieved by training the material for each shape at each temperature.
Metals and ceramics with thermally induced bidirectional shape-memory effect have had great application in medical implants, sensors, transducers, etc. Many present a risk however due to their high toxicity.
To obtain the effect, it is necessary to achieve a phase separation, one of these phases works as the trigger for the temporary form, using a transition temperature that can be Tm or Tg and in this effect is called TTrans. A second phase has the higher transition temperature and above this temperature the polymer melts and is processed by conventional methods.The ratio of the elements forming the phase separation largely regulates the TTrans transition temperature; this is much easier to control than in metallic alloys.
An example of this is the poly(ethylene oxide-ethylene terephthalate) or EOET copolymer. The polyethylene terephthalate (PET) segment has a relatively high Tg and its Tm is commonly referred to as the "hard" segment, whereas polyethylene ethylene oxide (PEO), has a relatively low Tm and Tg and is referred to as the "soft" segment. In the final polymer these segments separate into two phases in the solid state. PET has a high degree of crystallinity and the formation of these crystals provides for the flow and rearrangement of the PEO chains as they are stretched at temperatures higher than their Tm.
If crosslinking with slight vulcanization is desired, standardized methods for each polymer must be taken into account. In the case of PCO, for example, it is a polymer without shape-shape-memory effect because it does not present a clear "plateau", but the addition of a minimum amount of peroxide (~1%) provides PCO with all the requirements to present this effect.
Some polymers fatigue first, so each system can be evaluated with a simple experiment that consists of programming the system 10 or 20 times in a row and measuring the recovery in % and time.
Polymers that can crystallize are (with the exception of PP) guarantee to obtain this effect, mainly due to their ordering capacity, which is reflected in the crystallinity, the crystals have affinity for their constituent elements and form new bonds these achieve anchoring forces that give stability to the temporary form.
To analyze the behavior of the crystals in this type of polymers, the WAXS and DSC techniques are used; these techniques help to determine what percentage of the polymer are crystals and how they are organized. This is due to the fact that the crystallinity decreases as the crosslinking increases, since the chains lose the ability to arrange themselves and order is essential to achieve crystallinity.
A second problem present when crosslinking molecules is melting, since an excess of crosslinking modifies the molecule in such a way that it stops melting (similar to a thermoset) and therefore the temporary shape cannot be obtained.
The control of curing either by electromagnetic waves or with peroxides is very important since it increases the TTrans and decreases the crystallinity, determining factors in the shape-shape-memory effect.
In the case of biocompatible semicrystalline systems such as poly(ε-caprolactone) and poly(n-butyl acrylate), crosslinked by photopolymerization it has been reported that the crystallization behavior is affected by the cooling rate, as in any other semicrystalline polymer, but the heat of crystallization remains independent of the cooling rate.
The influence of the crosslinking of the molecules, the cooling rate and the crystallization behavior are specific to each system and impossible to enumerate since the synthesis possibilities are almost infinite.
Crystallizable polymers such as oligo(ε-caprolactone) can have amorphous segments such as poly(n-butyl acrylate) and the molecular mass ratio of each determine the behavior of the system in programming temporary form and recovery to permanent form.
If the polymeric system is amorphous, then the anchor points of the crystalline structure are not available and the only way to ensure the stability of the temporary shape is through chain entanglements (physical entanglements and not chemical crosslinking), in addition to the possibility of crosslinking.
In the glassy state, the movements of the long chain segments are frozen, the movements of these segments depend on an activation temperature that brings the polymer to a smoothing and elastic state, the rotation on the carbon bonds and the movements of the chains no longer have strong impediments to accommodate and acquire the conformation that requires less energy, the chains then "unravel" forming random strings, without order and therefore with higher entropy.
If a polymer sample is stretched for a short time in the elastic range, when the load is removed, the sample will recover its original shape, but if the load remains for a sufficiently long period, the chains rearrange and the original shape is not recovered, the result is an irreversible deformation, also called relaxation process (in this case: creep).
In order for a polymer to exhibit the thermally induced shape-memory effect, it is necessary to fix the chains with anchor points to avoid these relaxation processes that inelastically modify the system.
Amorphous polymers do not have a crystallization temperature (Tm) like semi-crystalline polymers and have only a glass transition temperature (Tg). This has a decisive influence on the behavior of shape-shape-memory polymer systems.
A crystalline copolymer system alone can result in the crosslinker-treated copolymer losing its crystallinity and becoming practically amorphous.
An amorphous polymer depends on the level of crosslinking or the degree of polymerization to exhibit this effect. In the case of poly(norbornene), which is a linear, amorphous polymer, with a content of 70 to 80% of trans bonds in commercial products, molecular mass of approximately 3x106 g mol−1 and Tg of approximately 35 to 45°C. Because it achieves an unusually high degree of polymerization, chain entanglements can be relied upon as anchor points to achieve the thermally induced shape-memory effect. Therefore, this polymer relies solely on physical anchor points. When heated up to Tg, the material abruptly changes from a rigid state to a tapered state (softens). To achieve the effect, the shape must be changed rapidly to avoid rearrangement of the segments of the polymer chains and immediately cool the material also very rapidly below Tg. Reheating the material back to Tg will show the recovery of the original shape.
In designing copolymers for thermally induced shape-memory effect it is very important to keep in mind that a slight change in chemical structure (cis/trans ratios, tacticity, molecular mass, etc.) produces a significant change in the shape-memory polymer. An example is the copolymer of poly(methylmethacrylate-co-methacrylic acid) or poly(MAA-co-MMA) compared to poly(MAA-co-MMA)-PEG, where PEG is short for poly(ethylene glycol) which forms complexes in the copolymer.
Changes in the morphology of the material including PEG provide shape-memory effect to the copolymer, showing two phases, the three-dimensional network providing a stable phase and the reversible phase formed by the amorphous part of the PEG-PMAA complexes. The complexes show a high modulus storage capacity, so when a PEG of higher molecular mass is introduced into the copolymer, an increase in the elastic modulus, higher modulus in the glassy state and faster recovery are observed.
Its properties can be studied with differential scanning calorimetry (DSC), wide-angle X-ray diffraction (WAXD) and dynamic mechanical analysis (DMA) techniques to determine its physicochemical arrangement.
Most of the applications of polymers with this effect are only suggestions for now, many possibilities have been proposed, but so far only a few have been used, the most important being medical devices and automotive elements, although the greatest success has been achieved with heat-shrinkable polyethylene, which is also an exception in the programming step, since it is processed in a different way.