Wide Range Of Strains Research Articles

Ultra-fast light repair, ultrasensitive, large strain detection range PDA@RGO/EVA composites fiber flexible strain sensor

The sensor fabricated from high-molecular polymer is soft, lightweight, and biocompatible; however, traditional high-molecular polymers suffer from viscoelasticity and poor cycle stability. To address these issues, it is essential to develop flexible matrix materials that can overcome viscoelasticity, ensuring high sensitivity and long-term use under large strains for next-generation wearable intelligent devices. In this study, ethylene-vinyl acetate (EVA) with a shape memory effect was utilized as the substrate for a flexible sensor，the shape memory effect of EVA can eliminate the residual strain generated by each long time of use to improve its service life. A polydopamine@reduced graphene oxide (PDA@RGO)/EVA fiber flexible strain sensor was fabricated through melt extrusion, swelling ultrasound, and in-situ polymerization techniques. The resulting sensor exhibits high sensitivity (gauge factor=1801.21), a wide strain detection range (strain = 193 %), and excellent stability and durability (2000 cycles). Notably, the PDA@RGO/EVA fiber flexible strain sensor demonstrates exceptional dual thermal and light repair functions, with light repair achieving a repair speed of 5 seconds, 100 % electrical performance repair efficiency, and perfect consistency in relative resistance response before and after repair. Furthermore, the PDA@RGO/EVA strain sensor can monitor finger and wrist movements in real-time with high accuracy, highlighting its significant potential application in the wearable technology field.

Characterization of quantum dot-like emitters in programmable arrays of nanowrinkles of 1L-WSe2

When combined with nanostructured substrates, two-dimensional semiconductors can be engineered with strain to tailor light–matter interactions on the nanoscale. Recently, room-temperature nanoscale exciton localization with controllable wrinkling in 1L-WSe2 was achieved using arrays of gold nanocones. Here, the characterization of quantum dot-like states and single-photon emitters in the 1L-WSe2/nanocone system is reported. The nanocones induce a wide range of strains, and as a result, a diverse ensemble of narrowband, potential single-photon emitters is observed. The distribution of emitter energies reveals that most reside in two spectrally isolated bands, leaving a less populated intermediate band that is spectrally isolated from the ensembles. The spectral isolation is advantageous for high-purity quantum light emitters, and anti-bunched emission from one of these states is confirmed up to 25 K. Although the spatial distribution of strain is expected to influence the orientation of the transition dipoles of the emitters, multimodal emission polarization anisotropy and atomic force microscopy reveal that the macroscopic orientation of the wrinkles is not a good predictor of dipole orientation. Finally, the emission is found to change with thermal cycling from 4 to 290 K and back to 4 K, highlighting the need to control factors such as temperature-induced strain to enhance the robustness of this quantum emitter platform. The initial characterization here shows that controlled nanowrinkles of 1L-WSe2 generate quantum light in addition to uncovering potential challenges that need to be addressed for their adoption into quantum photonic technologies.

Highly compressible porous polyethyleneimine/chitosan composite aerogel with excellent mechanical properties as wide detection range sensors for human motion monitoring

AbstractBiomass three‐dimensional composite aerogels have garnered significant attention in the realm of wearable electronic skin owing to their favorable properties, including excellent human compatibility, environmentally benign degradability, and continuous porous architecture. However, conventional biomass aerogels suffer from inadequate mechanical flexibility, susceptibility to irreversible deformation under high compressive stress, and limited reusability, thereby constraining their applicability in sensing technologies. To address these limitations, this study presents the development of porous CCS/KH560/PEI/CNT‐COOH (CKPC) composite aerogels through a freeze–drying process. Chemical crosslinking was achieved using silane coupling agent (KH560) with carboxymethyl chitosan (CCS) and polyethyleneimine (PEI), while carboxylated carbon nanotubes (CNT‐COOH) were incorporated as conductive fillers. This approach successfully overcame the issues of poor mechanical properties, low elasticity, and unbalanced sensitivity‐sensing range trade‐off in chitosan‐based aerogel sensors. The results revealed that the porous CKPC aerogels exhibited a remarkable mechanical compressive strain of 86.3% while maintaining structural integrity post‐unloading. The CKPC composite aerogel‐based sensor demonstrated a high sensitivity of 42.9 within a wide strain range of 60%–76.3%, accompanied by a stable and repeatable electrical signal response across varying strains. The porous structure of the CKPC conductive aerogel sensor holds promising applications in human motion monitoring and flexible electronics.

A high-sensitivity balloon-type optical fiber sensor enables wide-range strain sensing with the assistance of CNN

A balloon-type optical fiber sensor (OFS) for strain measurement was proposed, and the measurement range was significantly increased with the assistance of convolutional neural networks (CNN). The presented OFS was prepared by bending a Mach-Zehnder structure based on polarization-maintaining fibers into a balloon-type, which exhibits a sensitivity of 26.3 pm/με under the strain range from 0 to 300 με. The CNN-based signal analysis method can effectively extract the data information in the spectral, and the strain range that can be measured is greatly enlarged to 0–2000 με, while the accuracy of the measurement can be guaranteed. Further, the temperature sensitivity of the OFS is −0.0252 nm/°C; the lower temperature sensitivity can effectively suppress the crosstalk problem caused by temperature changes during strain measurement. The proposed method remarkably increases the strain measurement range of OFS, which is conducive to the application and development of OFSs.

Linear Film Strain Sensors with Nanosphere‐on‐Fiber Hetero‐Modulus Microstructure for Human‐Bionic Finger Interfacing

AbstractStretchable film strain sensors show potential applications in healthcare and human‐machine interfacing, while poor signal linearity restricts their practical applications owing to inaccurate and instable strain indication. Signal sensitivity and linearity can be improved via constructing hetero‐modulus microstructure on elastomeric substrate to some extent, though it is challenging to construct hetero‐structure with distinct modulus differences for electrical signal linearity modulation over a wide strain range. Herein, a simple strategy is proposed to tune signal sensitivity, linearity, and detection range of stretchable strain sensors by adjusting the distribution of rigid polystyrene (PS) nanospheres coated on electrospun thermoplastic polyurethane (TPU) fiber mats. Heterostructure characteristics can be controlled by spray coating times of PS nanospheres, which are immobilized onto the fiber mats by weak swelling of TPU and the linking layer of reduced graphene oxide (rGO) between TPU and PS induced by hydrogen bonding and π–π stacking. Relatively, the sensors with moderate spray coating times of PS nanospheres show balanced signal sensitivity and linearity over a strain range of 0–80%, as well as fast response to tensile strain and good signal reproducibility. Such elastomeric film strain sensors can be used for monitoring physiological activities and interfacing human hand and bionic fingers.

Evaluation of the Humoral Response after Immunization with a Chimeric Subunit Vaccine against Shiga Toxin-Producing Escherichia coli in Pregnant Sows and Their Offspring.

Shiga toxin-producing Escherichia coli (STEC) poses a significant public health risk due to its zoonotic potential and association with severe human diseases, such as hemorrhagic colitis and hemolytic uremic syndrome. Ruminants are recognized as primary reservoirs for STEC, but swine also contribute to the epidemiology of this pathogen, highlighting the need for effective prevention strategies across species. Notably, a subgroup of STEC that produces Shiga toxin type 2e (Stx2e) causes edema disease (ED) in newborn piglets, economically affecting pig production. This study evaluates the immunogenicity of a chimeric protein-based vaccine candidate against STEC in pregnant sows and the subsequent transfer of immunity to their offspring. This vaccine candidate, which includes chimeric proteins displaying selected epitopes from the proteins Cah, OmpT, and Hes, was previously proven to be immunogenic in pregnant cows. Our analysis revealed a broad diversity of STEC serotypes within swine populations, with the cah and ompT genes being prevalent, validating them as suitable antigens for vaccine development. Although the hes gene was detected less frequently, the presence of at least one of these three genes in a significant proportion of STEC suggests the potential of this vaccine to target a wide range of strains. The vaccination of pregnant sows led to an increase in specific IgG and IgA antibodies against the chimeric proteins, indicating successful immunization. Additionally, our results demonstrated the effective passive transfer of maternal antibodies to piglets, providing them with immediate, albeit temporary, humoral immunity against STEC. These humoral responses demonstrate the immunogenicity of the vaccine candidate and are preliminary indicators of its potential efficacy. However, further research is needed to conclusively evaluate its impact on STEC colonization and shedding. This study highlights the potential of maternal vaccination to protect piglets from ED and contributes to the development of vaccination strategies to reduce the prevalence of STEC in various animal reservoirs.

Nanocomposite hydrogel for skin motion sensing – An antifreezing, nanoreinforced hydrogel with decorated AuNP as a multicrosslinker

In this study, we present a nanocomposite hydrogel designed for skin motion sensing. The hydrogel is based on poly(acrylamide) crosslinked with gold nanoparticles covalently bound to the polymer matrix, yielding a robust, highly elastic and conductive material. The choice of amino acid derivative – N,N’-diacryloylcystine salt (BISS) – as a crosslinker allows for the introduction of gold nanoparticles, due to the presence of sulfide groups in its structure. During the nanoparticle modification process, covalent bonds between gold and sulfur atoms are formed as the disulfide bond is cleaved. In result of this self-assembly process, a multifunctional Au–BISS crosslinker is formed, enhancing the material’s mechanical properties and introducing electrical conductivity. To confer anti-freezing properties and limit water evaporation, a binary mixture of water and glycerol was used. The resultant hydrogel exhibits high elasticity, strain sensitivity across a wide strain range and various types of deformation (elongation, bending, compression) with exceptional response time (120 ms) and recovery time (90 ms). The material’s cold-resistance, resilience, and conductivity make it well-suited for real-time monitoring of joint movements and speech recognition, with potential applications in electronic skin and healthcare monitoring devices.

Ag–thiolate interactions to enable an ultrasensitive and stretchable MXene strain sensor with high temporospatial resolution

High-sensitivity strain sensing elements with a wide strain range, fast response, high stability, and small sensing areas are desirable for constructing strain sensor arrays with high temporospatial resolution. However, current strain sensors rely on crack-based conductive materials having an inherent tradeoff between their sensing area and performance. Here, we present a molecular-level crack modulation strategy in which we use layer-by-layer assembly to introduce strong, dynamic, and reversible coordination bonds in an MXene and silver nanowire-matrixed conductive film. We use this approach to fabricate a crack-based stretchable strain sensor with a very small sensing area (0.25 mm2). It also exhibits an ultrawide working strain range (0.001–37%), high sensitivity (gauge factor ~500 at 0.001% and >150,000 at 35%), fast response time, low hysteresis, and excellent long-term stability. Based on this high-performance sensing element and facile assembly process, a stretchable strain sensor array with a device density of 100 sensors per cm2 is realized. We demonstrate the practical use of the high-density strain sensor array as a multichannel pulse sensing system for monitoring pulses in terms of their spatiotemporal resolution.

Unified Understanding of Nonlinear Rheology near the Jamming Transition Point.

When slowly sheared, jammed packings respond elastically before yielding. This linear elastic regime becomes progressively narrower as the jamming transition point is approached, and rich nonlinear rheologies such as shear softening and hardening or melting emerge. However, the physical mechanism of these nonlinear rheologies remains elusive. To clarify this, we numerically study jammed packings of athermal frictionless soft particles under quasistatic shear γ. We find the universal scaling behavior for the ratio of the shear stress σ and the pressure P, independent of the preparation protocol of the initial configurations. In particular, we reveal shear softening σ/P∼γ^{1/2} over an unprecedentedly wide range of strain up to the yielding point, which a simple scaling argument can rationalize.

Mussel-adhesive chemistry inspired conductive hydrogel with self-adhesion, biocompatibility, self-recovery and fatigue-resistance performances as flexible sensing electronics

Conductive hydrogels are ideal candidates for wearable strain sensors due to their intrinsic stretchability and conductivity. However, it’s still a challenge to fabricate a conductive hydrogel with a combination performance of high mechanical strength, self-adhesion, sensitivity, self-recovery capability, fatigue-resistant ability and biocompatibility. Herein, a dual-network hydrogel (TG/P-LP) composed of 2,2,6,6-tetra-methylpiperidine-1-oxyl (TEMPO)-oxidized cellulose nanofibers (TOCNs) supported graphene (GN), Laponite-oxidized polydopamine (LP) and polyacrylic acid-co-poly acrylamide (P) hydrogel matrix was synthesized via a facile in-situ radical polymerization process. The optimized biocompatible TG/P-LP hydrogel exhibits a high mechanical strength, self-adhesive performance, intrinsic self-recovery capability (95.7 % in 60 min) and anti-fatigue property. The hydrogel-based strain sensor exhibits a wide strain range (0 ∼ 600 %) and a high sensitivity (GF = 12). This work designs a novel hydrogel-based sensor with excellent mechanical properties, long-term fatigue resistance, high strain sensitivity and wearability, demonstrating enormous potential in the applications of human motion detection and human–machine interaction.

Ultra-sensitive strain sensor with film-nanowire double layers for health monitoring and smart clothing

Flexible wearable strain sensors are becoming increasingly popular due to their ability to monitor physiological signals and to detect motion in a wide range of applications. However, the development of strain sensors with high sensitivity and wide sensing range remains a challenge. Herein, a film-nanowire double sensoring layer structure (FNDLS) crack strain sensor with high sensitivity, wide strain range and fast response is proposed. The FNDLS with hierarchical synergistic are integrated onto fabrics using a heat pressing process. The FNDLS has a very low initial resistance and a high density of channel cracks to have the high sensitivity of the strain sensor and to extend the strain range of the strain sensor through the synergistic bridging effect of the AgNWs. Due to this structure, the sensitivity of the sensor can reach 70945, the strain range can reach about 40 %, and response time is less than 129 ms. Furthermore, the sensor demonstrates exceptional cycling stability and favourable frequency characteristics. Its superior performance makes it suitable for monitoring pulse waves and detecting motion through smart clothing.

A universal solvent-replacement strategy to convert alginate hydrogels into mechanically strong and transparent alginate eutectogels for sensitive strain sensors

Eutectogels based on natural polymers have attracted significant attention as an alternative to easily dehydrated hydrogels and expensive ionogels in the development of flexible strain sensors. The feasibility of employing eutectogels derived from pure natural polymers could be greatly enhanced if their mechanical properties satisfy the requirements of applications. Herein, alginate eutectogels (AEs) with high mechanical properties (tensile strain 217 % and strength 2.26 MPa at fracture), and excellent transparency (over 90 %) are acquired via CaCl2 inducing ionic crosslinking and subsequent deep eutectic solvents (DESs, composed of glycerol and choline chloride) initiating physical crosslinking with a universal solvent- replacement strategy. Among them, sodium alginate, a natural polysaccharide polymer, is selected as representative supporting scaffolds and forms water-insoluble alginate hydrogels (AHs) in CaCl2 coagulation bath. The exchange of DESs with water of AHs not only restrengthens the polymer network by physical crosslinking, but also endows the obtained AEs with long-term solvent retention and high temperature resistance. In addition, the AEs not only have high reliability but also exhibit better linear sensitivity in a wide strain range (0–200 %). In particular, the AEs display multiple sensitivity to stretching, bending, and human motions, demonstrating feasibility as sensitive strain sensors.

High‐performance XSBR‐based flexible strain sensors enabled by pleated microcrack structure

AbstractFlexible strain sensors are attracting attention in areas such as medical monitoring sensing and rehabilitation therapy monitoring due to their powerful ability to sense, process, transmit and display complex information. However, it is an urgent challenge to realize the trade‐off between excellent performances such as high sensitivity, high linearity, wide strain sensing range and high durability. Herein, we prepare stretchable conductive composites with wrinkle composite micro‐crack structure by combining carboxystyrene butadiene rubber (XSBR) layer and carboxymethyl cellulose@Ag nanowire‐CNTs (CMC@AgNWs‐CNTs) conductive layer. Based on interfacial interactions, it can be adapted to different needs by adjusting the thickness of the strain sensing layer. When the thickness of the strain sensing layer is 4 μm, the strain sensor has a wide sensing range (strain capacity up to 300%) and high sensitivity (strain sensing factor of 484). At a thickness of 8 μm, the strain sensing performance exhibits a wide strain range, high linear fit and good cyclic stability. This work provides a new research idea to improve the comprehensive performance of flexible strain sensors and the contradiction between wide sensing range, high sensitivity and high linearity.

Dynamic globularization behavior of the dual-phase TiZrV medium entropy alloy during hot working

Globularization is an advantageous way to improve the formability of dual-phase materials. Dynamic globularization behavior of the TiZrV medium entropy alloy (MEA) with dual-phase was investigated at the temperature range of 500 ℃ ∼ 700 ℃ and strain rate of 0.1 s-1 ∼ 10 s-1 by the double-cone compression test. The finite element software was used to simulate the hot compression process of the double-cone specimen. Transmission electron microscope (TEM) was used to study the deformation microstructure features. The double-cone test can produce a wide strain range and corresponding deformation microstructure. The highest globularization ratio of 72.4% was obtained under the strain of about 0.88 at 500 ℃ and 10 s-1. The hot deformation mechanism map in the temperature range of 500 ℃ ∼ 700 ℃ and the strain range of 0.2 ∼ 1.2 at 10 s-1 was constructed by combining the double-cone test with finite element simulation. The hot deformation mechanism map is divided primarily into two parts. At 500 ℃, in the strain region of 0.2 ∼ 0.88, the deformation mechanism is dynamic recovery (DRV), and in the strain region of 0.88 ∼ 1.2, the deformation mechanism is dynamic recrystallization (DRX). It is considered that DRX plays a key role in dynamic globularization of the TiV phase during hot working and its production is summarized.

Broadly Reactive Nanobody Targeting the H3 Hemagglutinin of the Influenza A Virus.

Monoclonal antibodies and recombinant antibody fragments are a very promising therapeutic tool to combat infectious diseases. Due to their unique paratope structure, nanobodies (VHHs) hold several advantages over conventional monoclonal antibodies, especially in relation to viral infections. Influenza A viruses (IAVs) remain a major threat to public health. The hemagglutinin (HA) protein is the main protective and immunodominant antigen of IAVs. In this study, three broadly reactive nanobodies (D9.2, E12.2, and D4.2) to H3N2 influenza strains were isolated and Fc-fusion proteins (VHH-Fcs) were obtained and characterized in vitro. This modification improved the nanobodies' binding activity and allowed for their interaction with a wider range of strains. The D9.2-Fc antibody showed a 100% protection rate against mortality in vivo in a mouse lethal model. Furthermore, we demonstrated that the observed protection has to do with Fc-FcγR interactions. These results indicate that D9.2-Fc can serve as an effective antiviral agent against the H3N2 influenza infection.

Glycyrrhizic Acid Nanoparticles Subside the Activity of Methicillin-Resistant Staphylococcus aureus by Suppressing PBP2a.

Staphylococcus aureus and methicillin-resistant Staphylococcus aureus (MRSA) are classified as high-risk infections that can lead to death, particularly among older individuals. Nowadays, plant nanoparticles such as glycyrrhizic acid are recognized as efficient bactericides against a wide range of bacterial strains. Recently, scientists have shown interest in plant extract nanoparticles, derived from natural sources, which can be synthesized into nanomaterials. Interestingly, glycyrrhizic acid is rich in antioxidants as well as antibacterial agents, and it exhibits no adverse effects on normal cells. In this study, glycyrrhizic acid nanoparticles (GA-NPs) were synthesized using the hydrothermal method and characterized through physicochemical techniques such as UV-visible spectrometry, DLS, zeta potential, and TEM. The antimicrobial activity of GA-NPs was investigated through various methods, including MIC assays, anti-biofilm activity assays, ATPase activity assays, and kill-time assays. The expression levels of mecA, mecR1, blaR1, and blaZ genes were measured by quantitative RT-qPCR. Additionally, the presence of the penicillin-binding protein 2a (PBP2a) protein of S. aureus and MRSA was evaluated by a Western blot assay. The results emphasized the fabrication of GA nanoparticles in spherical shapes with a diameter in the range of 40-50 nm. The data show that GA nanoparticles exhibit great bactericidal effectiveness against S. aureus and MRSA. The treatment with GA-NPs remarkably reduces the expression levels of the mecA, mecR1, blaR1, and blaZ genes. PBP2a expression in MRSA was significantly reduced after treatment with GA-NPs. Overall, this study demonstrates that glycyrrhizic acid nanoparticles have potent antibacterial activity, particularly against MRSA. This research elucidates the inhibition mechanism of glycyrrhizic acid, which involves the suppressing of PBP2a expression. This work emphasizes the importance of utilizing plant nanoparticles as effective antimicrobial agents against a broad spectrum of bacteria.

High-density, highly sensitive sensor array of spiky carbon nanospheres for strain field mapping

While accurate mapping of strain distribution is crucial for assessing stress concentration and estimating fatigue life in engineering applications, conventional strain sensor arrays face a great challenge in balancing sensitivity and sensing density for effective strain mapping. In this study, we present a Fowler-Nordheim tunneling effect of monodispersed spiky carbon nanosphere array on polydimethylsiloxane as strain sensor arrays to achieve a sensitivity up to 70,000, a sensing density of 100 pixel cm−2, and logarithmic linearity over 99% within a wide strain range of 0% to 60%. The highly ordered assembly of spiky carbon nanospheres in each unit also ensures high inter-unit consistency (standard deviation ≤3.82%). Furthermore, this sensor array can conformally cover diverse surfaces, enabling accurate acquisition of strain distributions. The sensing array offers a convenient approach for mapping strain fields in various applications such as flexible electronics, soft robotics, biomechanics, and structure health monitoring.

High-Spatial-Resolution and Wide-Range Strain Distributed Sensor Based on Exposed-SMF Using Efficient Adaptive Zero Padding

High-Spatial-Resolution and Wide-Range Strain Distributed Sensor Based on Exposed-SMF Using Efficient Adaptive Zero Padding

Self‐Repairable Hybrid Piezoresistive‐Triboelectric Sensor Cum Nanogenerator Utilizing Dual‐Dynamic Reversible Network in Mechanically Robust Modified Natural Rubber

AbstractThe greener alternatives to tactile‐integrated multimodal sensors with self‐powered and self‐healing abilities are highly desirable for all‐in‐one autonomous sensing systems, particularly impressive in diverse application ranges including smart home, healthcare, and e‐skin. The dynamically self‐healable, stretchable piezoresistive sensors, and triboelectric nanogenerators (TENGs) reported herein are constructed by a facile, industrially viable method of grafting imidazolium ions on epoxidized natural rubber (ENR) backbone. Owing to cation‐π and π–π interaction between the percolated carbon nanotubes (CNTs)‐network and the imidazolium ions formed by non‐covalent interactions, the interfacial adhesion between the filler and elastomer is shown to improve considerably. The sensors show high piezoresistive strain sensitivity, reversible ionic network‐assisted self‐healability (efficiency ≈80%) and wide‐ranging detectability for precise monitoring of human movements. Both the healed and pristine sensors feature low hysteresis and stable electrical outputs over a wide strain range (≤200%). While achieving rapid self‐healing efficiency, the substrates are shown to exhibit remarkable robustness for harsh climates owing to significant mechanical toughness. Supported by excellent triboelectric tactile sensitivity (2.12 V N−1), the multifunctional TENG‐enabled sensor yields superior power density (0.16 mW cm−2). Moreover, the TENG module exhibits high force sensitivity and ease of operation that are considered versatile for all‐weather integrated tactile solutions for future technology.

Reversible reorientation of martensite variants in stress-induced martensite aged Co35Ni35Al30 single crystals

The paper reports the temperature dependence of the reversible reorientation of martensite variants during loading/unloading along the [001]B2||[001]L10-direction in compression in stress-induced martensite (SIM) aged at 423 K for 0.5 h under a compressive stress of 500 MPa applied along the [110]B2||[100]L10-direction Co35Ni35Al30 single crystals. A wide temperature range of reversible strain from 203 K to 413 K (210 K) is observed due to the stabilisation of the tetragonal L10-martensite variant V1 ([001]B2||[001]L10) during SIM-aging in these single crystals. The reversible strain in the range of 157 K (203 K<Tt<As=Af=360 K) is because of the reorientation of the L10-martensite variants V1-V2/V3. The superelasticity at Tt>Af=360 K occurred due to the stress-induced B2-L10(V2/V3) martensitic transformation (MT). Rubber-like behaviour develops in the range of 52 K (203 K<Tt<Mf*=255 K) and is characterised by a narrow stress hysteresis of 13 MPa and a reversible strain of −12.0 % due to the movement of the twinning boundaries (reversible twinning) in L10-martensite. The reversible strain reaches −10.2 % in the temperature range from Mf*=255 K to As=Af=360 K. This strain is associated with a new mechanism of L10-martensite variant reorientation, which occurs through a sequence of reverse and forward stress-induced L10(V1)-B2-L10(V2/V3) MTs and leads to the stages on the stress–strain curves. The reverse L10(V1)-B2 MT at loading and forward B2-L10(V1) MT at unloading on the first stage of the stress–strain curves are characterised by low critical stresses of 8–23 MPa, a narrow stress hysteresis of 3–19 MPa and a completely reversible strain of −6.0 %, which is stable for 100 loading/unloading cycles.