Fatigue Resistance Properties Research Articles

A tough soft–hard interface in the human knee joint driven by multiscale toughening mechanisms

Joining heterogeneous materials in engineered structures remains a significant challenge due to stress concentration at interfaces, which often leads to unexpected failures. Investigating the complex, multiscale-graded structures found in animal tissue provides valuable insights that can help address this challenge. The human meniscus root-bone interface is an exemplary model, renowned for its exceptional fatigue resistance, toughness, and interfacial adhesion properties throughout its lifespan. Here, we investigated the multiscale graded mineralization structure and their strengthening mechanisms within the 30-micron soft-hard interface at the root-bone junction. This graded interface, featuring interdigitated structures and an exponential increase in modulus, undergoes a phase transition from amorphous calcium phosphate (ACP) to gradually matured hydroxyapatite (HAP) crystals, regulated by location-specific distributed biomolecules. In coordination with collagen fibril deformation and reorientation, the in situ tensile mechanical experiments and molecular dynamic simulations revealed that immature ACP particles debond from the collagenous matrix and translocate to dissipate energy, while the progressively matured HAP crystals with high stiffness pins propagating cracks, thereby enhancing both the toughness and fatigue resistance of the interface. To further validate our findings, we built biomimetic soft-hard interfaces with phase-transforming mineralization which exhibited boosted strength, toughness, and interface adhesion. This interface model is generalizable to other material joints and provides a blueprint for developing robust soft-hard composites across various applications.

Comprehensive Review: Optimization of Epoxy Composites, Mechanical Properties, & Technological Trends

Epoxy composites play a crucial role in modern materials technologies, with their exceptional properties such as high strength and thermal and chemical resistance, making them ideal for a wide range of industrial applications, including aerospace, automotive, construction, and energy. This review article provides a comprehensive overview of the current trends and advancements in epoxy composites, focusing on mechanical properties and their optimization. Attention is given to technological innovations, including the use of nanotechnologies, hybrid reinforcement, and eco-friendly materials, which are key to enhancing the performance and sustainability of these materials. The analysis shows that the introduction of nanomaterials, such as graphene, titanium dioxide, and silicon dioxide, can significantly improve the strength, fatigue resistance, and electrical properties of epoxy composites, opening new possibilities in advanced technologies. Another significant contribution is the development of hybrid composites, which combine different types of fibers, such as carbon, aramid, and glass fibers, enabling the optimization of key properties, including interlayer strength and delamination resistance. The article also highlights the importance of environmental innovations, such as bio-based resins and self-healing mechanisms, which enable more sustainable and long-term effective use of composites. The combination of theoretical knowledge with practical applications provides valuable guidance for designing materials with precisely defined properties for future industrial use. This text thus offers a comprehensive view of the possibilities of epoxy composites in the context of increasing demands for performance, reliability, and environmental sustainability.

Tri-Prism Origami Enabled Soft Modular Actuator for Reconfigurable Robots.

Soft actuators hold great potential for applications in surgical operations, robotic manipulation, and prosthetic devices. However, they are limited by their structures, materials, and actuation methods, resulting in disadvantages in output force and dynamic response. This article introduces a soft pneumatic actuator capable of bending based on triangular prism origami. The origami creases are crafted by utilizing fabrics to gain swift response and fatigue-resistant properties. By connecting two actuators in series, combined motions including extension and diversified compound bending can be achieved, facilitating control in complex scenarios. After modularizing the soft actuator via mortise and tenon structures, several actuators can be programmed to execute a variety of intricate tasks by adjusting the timing sequences of their contraction and expansion. We showcase its applications in reconfigurable robots, and the results confirm that such a design is adequate for flexibly performing tasks such as soft gripping, navigational movement, and obstacle avoidance. These findings highlight the significance of our actuator in developing soft robots for versatile tasks.

Poly(lactide)/poly(butylene adipate-co-terephthalate)/carbon nanotubes composites with robust mechanical properties, fatigue-resistance and dielectric properties.

A styrene-glycidylmethacrylate-1-allyl-3-vinylimidazole epoxy functionalized ionomer (EFI) was synthesized, and the EFI and carbon nanotubes (CNTs) were co-introduced into poly(lactide)/poly(butylene-adipate-co-terephtalate) (PLA/PBAT) blends to fabricate high performance composites with excellent mechanical properties, fatigue-resistance and dielectric properties. It is revealed that EFI can improve the interaction force between PLA and PBAT by inducing the interfacial crosslink reaction, thereby improving the melt strength of the samples. EFI can also refine the dispersion of CNT in the composites owing to the non-covalent force between EFI and CNT, promote the formation of filler network inside composites, which is demonstrated by DMA and rheological test results. The CNT can be anchored at the interface between PLA and PBAT owing to the interaction between EFI and CNT, and the synergistic effect of CNT and EFI on the interfacial structure and phase structure can significantly enhance the mechanical properties of the materials. When the CNT content is 3 wt%, the composite has a tensile strength of 30.4 MPa and an elongation at break of 279.3 %, which are 30 % and 48 % higher than that of PLA/PBAT blend, and it also exhibits excellent dielectric properties with a dielectric constant of 25.2 and a dielectric loss of 11.6. Moreover, the composites also have excellent fatigue resistance owing to the refined interfacial structure and compact CNT network.

Unexpected large remnant polarization in Sn-doped Bi4Ti3O12 ferroelectric film by chemical solution deposition

The A-site rare earth-doped Bi4Ti3O[Formula: see text] (BTO) has been highly interested in nonvolatile ferroelectric random memory devices, piezoelectric devices, electro-optical devices, capacitors, sensors, transducers, etc., due to its low coercive field and superior fatigue resistance properties. However, single B-site doping has not received corresponding attention. In this work, BTO and Bi4Ti[Formula: see text]Sn[Formula: see text]O[Formula: see text] (BTS) thin films were prepared by sol–gel method, in which the doping of Sn effectively restrained the grain growth and decreased the grain size, as well as diminished the formation of oxygen vacancies and enhanced the breakdown field. This leads to a significant enhancement of the ferroelectric properties of the BTO films. The final BTS films exhibit excellent saturation P–E loops with a remnant polarization (2[Formula: see text]) of 94.4[Formula: see text][Formula: see text]C/cm2 and a coercive field (2[Formula: see text]) of 0.69[Formula: see text]MV/cm at a maximum electric field of 2.8[Formula: see text]MV/cm. The ferroelectric fatigue and dielectric properties of BTS film were also characterized. The results suggest that doping of Sn at B-site can effectively improve the breakdown strength and enhance the ferroelectric properties of the BTO film.

Anomaly detection by X-ray tomography and probabilistic fatigue assessment of aluminum brackets manufactured by PBF-LB

The assessment of safety-critical components for fatigue applications is a key requirement for metal additive manufacturing (AM) applications. Material anomalies play a relevant role in determining the fatigue resistance properties of a component. X-ray computed tomography (CT) helps collect important information on these flaws, such as their size and position within a part.In this study, we discuss how to employ anomaly data detected on an AlSi10Mg bracket manufactured by laser-powder bed fusion to describe the prospective allowable life of a component under a given operating condition.A statistical analysis was conducted on the specimens and component to derive the correlation between different resolution scans and analyze the uncertainties of the micro-CT measurements. The full-scale non-destructive evaluation (NDE) can be constrained to large voxel sizes. Eventually, the authors proposed a fully probabilistic route for assessment instead of a simple deterministic assessment based on safety factors. This assessment enables designers to consider the uncertainties of the assessment (uncertainties of micro-CT detection and the model for fatigue strength).

A Stretchable Conductive Material with High Fatigue Resistance for Strain Sensors.

Intrinsically stretchable conductive materials based on elastic substrates and conductive components play important roles in biomedical applications, such as exercise rehabilitation monitoring and disease prediction. A persistent challenge is to combine high fatigue resistance with excellent mechanical properties in stretchable conductive materials. Herein, we present a stretchable conductive material with both good fatigue resistance and high tensile properties (∼3170%) based on poly(acrylic acid)-phytic acid-trehalose-polypyrrole (denoted as PPTP). The as-prepared PPTP hydrogel electrode showed no obvious cracking or delamination after 400 loading and unloading cycles and maintained good electrical signal transmission function after 1000 cycles. We further collected stable signals for human motion and handwriting using the stretchable hydrogel electrode as a strain sensor, demonstrating the potential application of the PPTP stretchable hydrogel electrode in biomedicine.

Continuous Phase Separation Induced Tough Hydrogel Fibers with Ultrahigh Conductivity for Multidimensional Soft Electronics

AbstractConductive hydrogel fibers exhibit great potential in soft robots, bioelectronics, and human–machine interfaces due to the unique combination of electrical conductivity, high water content, tissue‐like mechanical properties, and 1D structure. Despite significant advances in hydrogel technologies, the typical conductive hydrogel fibers show low conductivity (<10 S cm−1), weak mechanical properties, and water stability, which makes it challenging to satisfy the requirements of practical applications. Here, a facile strategy is proposed to construct hydrogel fibers with ultrahigh conductivity and toughness by exploiting the synergistic effects of freezing‐thawing, salting‐out, and drying‐annealing. The continuous phase separation induced by the combined processes results in hierarchical structures, promoting the formation of interconnected conductive networks and increasing the fiber's crystallinity and crystal domain size. The prepared conductive hydrogel fibers exhibited ultrahigh conductivity (≈958 S cm−1), excellent mechanical properties (strength (≈6.2 MPa), stretchability (>300%), and toughness (≈10 MJ m−2)), high water content (≈75%), outstanding water stability, and fatigue resistance properties. In addition, the processibility of conductive hydrogel yarns and fabrics are demonstrated and their potential application in bioelectronics. Overall, this work presents a preparation strategy for conductive hydrogel fibers, which will facilitate the advancement of soft electronics and may inspire structural construction in other polymers.

Investigation of torsional and fatigue resistance properties based on triply periodic minimal surfaces (TPMS)

Abstract Triply periodic minimal surfaces (TPMS) are algebraic surfaces found in nature, defined by implicit functions, and exhibit exceptional properties in various fields such as mechanics, computer graphics, and tissue engineering. This study focuses on four common minimal surface structures: Gyroid, Diamond, I-WP, and Schwarz P structures, and presents two methods for converting these surfaces into TPMS cells. These four surface structures are converted into TPMS cells, which are then organized into TPMS cylindrical units for finite element analysis. Through a comparison of the torsional mechanical properties of different minimal surfaces using the finite element method, the stress-strain curves of TPMS were generated. The findings suggest that the Schwarz P cylindrical structure remains within the elastic deformation stage under the same load, with a stress-load curve exhibiting a smaller slope, indicating superior torsional resistance. Additionally, a fatigue strength analysis of various minimal surface structures revealed that, under equivalent load conditions, the fatigue life of the Schwarz P cylindrical structure tends towards infinity.

Substituent effects on the mechanochromic behaviour of pyrene-based AIEgens

It is extremely significant and desirable to integrate the fascinating properties of mechanochromism and aggregation-induced emission (AIE) in one simple molecule. Herein, pyrene-based aggregation-induced emission luminogens (AIEgens) with mechanofluorochromic (MFC) properties solve the traditionally existing aggregation-caused quenching (ACQ) challenge. Three cyanoethylene-functionalized pyrene-based derivatives were designed and synthesized. All compounds exhibit remarkable aggregation-enhanced emission (AEE) activity by a 3–20 times enhancement in mixed H2O/THF solutions. More importantly, high fluorescence efficiency was recorded in the solid state, especially for the luminogen 2c, with more than 200 times observed increased efficiency from 0.3% in solution to 69.8% in the solid state. Meanwhile, excellent mechanochromism properties and reversibility against the grinding treatment was systematically investigated. The excellent fatigue resistance properties are a necessity for potential applications in the field of anti-counterfeiting fluorescent inks and for the encryption of security information.

DEVELOPMENT OF HYDROGENATED SBR-BASED VULCANIZATE WITH SUPERIOR TIRE TREAD PERFORMANCE

ABSTRACT Currently, the tire industry is exploring eco-friendly tires with improved rolling resistance, traction, abrasion resistance, and fatigue properties. The present study investigates the potentiality of the hydrogenated styrene butadiene rubber (HSBR), a special and modified grade of styrene butadiene rubber (SBR) as a tyre tread material. The rheological, mechanical, dynamic mechanical, abrasion resistance, fatigue resistance, aging resistance and ozone resistance properties of the developed HSBR-based composites were critically evaluated and compared with those of conventional rubbers such as natural rubber (NR), emulsion styrene butadiene rubber (ESBR) and solution styrene butadiene rubber (SSBR) based composites. Interestingly, the HSBR-based vulcanizates exhibited superior modulus, tensile strength, abrasion resistance, fatigue crack growth resistance, resistance to thermo-oxidative aging, and ozone resistance as compared to the conventional SBR–based vulcanizates. The modulus at 300% elongation of the HSBR-based vulcanizate was approximately 74% and 11% higher than that of the ESBR- and SSBR-based composites, respectively, whereas the improvements in tensile strength were approximately 88% and 64% and the improvements in abrasion resistance were approximately 250% and 200% than that of the ESBR and SSBR vulcanizates, respectively. The tensile strength and fatigue resistance characteristics of the HSBR vulcanizate were also nearly similar to those of the NR vulcanizate. The findings demonstrate that HSBR can be a potential tire tread material with robust physico-mechanical properties and durability.

Fabrication of anti-freezing and self-healing hydrogel sensors based on carboxymethyl guar gum and poly(ionic liquid)

As classical soft materials, conductive hydrogels have attracted wide attention in the field of strain sensors due to their unique flexibility and conductivity. However, there are still challenges in developing conductive hydrogels with comprehensive mechanical strength, self-healing ability and sensitive sensing properties. In this paper, a novel PAV/CMGG hydrogel was prepared by a simple one-pot method through the introduction of 1-vinyl-3-butylimidazolium bromide (VBIMBr), acrylic acid (AA), carboxymethyl guar gum (CMGG) and AlCl3. The coordination bond between Al3+ and –COO− groups on PAA and CMGG, the hydrogen bond between PAA and CMGG, and the electrostatic interaction between [VBIM]+ and –COO− endow the hydrogel with good mechanical properties, self-recovery ability, fatigue resistance and great self-healing properties. PAV/CMGG hydrogel had good conductivity of 2.31 S/m which could successfully light up the bulb. The hydrogel as the strain sensor had not only a wide strain sensing capability (strain ranging from 0 to 800 %), but also a high strain sensitivity (gauge factor (GF) = 28.50 for the strain ranging from 600 to 800 %). This study can provide inspiration for the construction of new high-performance flexible sensors.

Topological Rearrangement-Induced Mesoscale Phase Redistribution to Enhance the Fatigue Resistance of Polymer Blends.

Maintaining a high modulus to simultaneously withstand deformation and increase fatigue resistance to restrict crack propagation in a material presents a significant challenge. In this work, a straightforward strategy was developed to address this issue in polymers. A dynamic network was incorporated into a permanent one prior to the formation of the latter, and two incompatible polymer networks were created to prevent common phase separation. The mechanical and fatigue resistance properties were substantially enhanced by the exact modulation of the soft and hard phase distribution by precise control over the densities of dynamic and permanent networks as well as the number of reprocessing steps. The experimental results demonstrated a nearly 9-fold increase in the fatigue life of polyurethane compared with traditional design methods and a 2.5 times increase in modulus. This strategy shows potential for the design of fatigue-resistant thermosetting and thermoplastic materials. The results offer new insight into the development of durable, high-performance materials that are reprocessable and compatible.

Super-Durable, Tough Shape-Memory Polymeric Materials Woven from Interlocking Rigid-Flexible Chains.

Developing advanced engineering polymers that combine high strength and toughness represents not only a necessary path to excellence but also a major technical challenge. Here for the first time a rigid-flexible interlocking polymer (RFIP) is reported featuring remarkable mechanical properties, consisting of flexible polyurethane (PU) and rigid polyimide (PI) chains cleverly woven together around the copper(I) ions center. By rationally weaving PI, PU chains, and copper(I) ions, RFIP exhibits ultra-high strength (twice that of unwoven polymers, 91.4±3.3MPa), toughness (448.0±14.2MJ m-3), fatigue resistance (recoverable after 10000 cyclic stretches), and shape memory properties. Simulation results and characterization analysis together support the correlation between microstructure and macroscopic features, confirming the greater cohesive energy of the interwoven network and providing insights into strengthening toughening mechanisms. The essence of weaving on the atomic and molecular levels is fused to obtain brilliant and valuable mechanical properties, opening new perspectives in designing robust and stable polymers.

Mechanically Robust and Electrically Conductive Hybrid Hydrogel Electrolyte Enabled by Simultaneous Dual In Situ Sol-Gel Technique and Free Radical Copolymerization.

Mechanically robust and ionically conductive hydrogels poly(acrylamide-co-2-acrylamido-2-methylpropanesulfonate-lithium)/TiO2/SiO2 (P(AM-co-AMPSLi)/TiO2/SiO2) with inorganic hybrid crosslinking are fabricated through dual in situ sol-gel reaction of vinyltriethoxysilane (VTES) and tetrabutyl titanate (TBOT), and in situ radical copolymerization of acrylamide (AM), 2-acrylamide-2-methylpropanesulfonate-lithium (AMPSLi), and vinyl-SiO2. Due to the introduction of the sulfonic acid groups and Li+ by the reaction of AMPS with Li2CO3, the conductivity of the ionic hydrogel can reach 0.19Sm-1. Vinyl-SiO2 and nano-TiO2 are used in this hybrid hydrogel as both multifunctional hybrid crosslinkers and fillers. The hybrid hydrogels demonstrate high tensile strength (0.11-0.33MPa) and elongation at break (98-1867%), ultrahigh compression strength (0.28-1.36MPa), certain fatigue resistance, self-healing, and self-adhesive properties, which are due to covalent bonds between TiO2 and SiO2, as well as P(AM-co-AMPSLi) chains and SiO2, and noncovalent bonds between TiO2 and P(AM-co-AMPSLi) chains, as well as the organic frameworks. Furthermore, the specific capacitance, energy density, and power density of the supercapacitors based on ionic hybrid hydrogel electrolytes are 2.88Fg-1, 0.09Whkg-1, and 3.07kWkg-1 at a current density of 0.05Ag-1, respectively. Consequently, the ionic hybrid hydrogels show great promise as flexible energy storage devices.

A super-stretchable and anti-fatigue silicone gel by regulating chain entanglement and cross-link density

Applications of silicone gel in flexible devices and soft machines require it to maintain excellent stretchability and antifatigue. However, the reported fatigue threshold of traditional silicone gels is in the range of 1–100 J m−2 and the stretchability below 2000 %. Herein, we report a simple strategy for constructing soft polydimethylsiloxane gels, which possesses high stretchability up to 8300 %, and high fatigue resistance (321 J m−2). This is achieved by controlling the ratio of chemical crosslinking and physical entanglement in the polydimethylsiloxane gels. The symbiotic relationship of this combination includes: extending the polymer chains helps them unfold to increase softness and intrinsic toughness; controlling the physical entanglement and chemical cross-linking helps to further increase the tensile rate and fatigue threshold, and adding small-molecule dimethyl PDMS as a solvent further increases fatigue resistance and tensile properties. This work provides a facile approach for developing super-stretchable and anti-fatigue silicone gel, which promises wide range of applicant in flexible devices and soft machines.

Dynamic Metal-Coordinated Adhesive and Self-Healable Antifreezing Hydrogels for Strain Sensing, Flexible Supercapacitors, and EMI Shielding Applications.

Dynamic metal-coordinated adhesive and self-healable hydrogel materials have garnered significant attention in recent years due to their potential applications in various fields. These hydrogels can form reversible metal-ligand bonds, resulting in a network structure that can be easily broken and reformed, leading to self-healing capabilities. In addition, these hydrogels possess excellent mechanical strength and flexibility, making them suitable for strain-sensing applications. In this work, we have developed a mechanically robust, highly stretchable, self-healing, and adhesive hydrogel by incorporating Ca2+-dicarboxylate dynamic metal-ligand cross-links in combination with low density chemical cross-links into a poly(acrylamide-co-maleic acid) copolymer structure. Utilizing the reversible nature of the Ca2+-dicarboxylate bond, the hydrogel exhibited a tensile strength of up to ∼250 kPa and was able to stretch to 15-16 times its original length. The hydrogel exhibited a high fracture energy of ∼1500 J m-2, similar to that of cartilage. Furthermore, the hydrogel showed good recovery, fatigue resistance, and fast self-healing properties due to the reversible Ca2+-dicarboxylate cross-links. The presence of Ca2+ resulted in a highly conductive hydrogel, which was utilized to design a flexible resistive strain sensor. This hydrogel can strongly adhere to different substrates, making it advantageous for applications in flexible electronic devices. When adhered to human body parts, the hydrogel can efficiently detect limb movements. The hydrogel also exhibited excellent performance as a solid electrolyte for flexible supercapacitors, with a capacitance of ∼260 F/g at 0.5 A/g current density. Due to its antifreezing and antidehydration properties, this hydrogel retains its flexibility at subzero temperatures for an extended period. Additionally, the porous network and high water content of the hydrogel impart remarkable electromagnetic attenuation properties, with a value of ∼38 dB in the 14.5-20.5 GHz frequency range, which is higher than any other hydrogel without conducting fillers. Overall, the hydrogel reported in this study exhibits diverse applications as a strain sensor, solid electrolyte for flexible supercapacitors, and efficient material for electromagnetic attenuation. Its multifunctional properties make it a promising candidate for use in various fields as a state-of-the-art material.

A strategy for tough and fatigue-resistant hydrogels via loose cross-linking and dense dehydration-induced entanglements

Outstanding overall mechanical properties are essential for the successful utilization of hydrogels in advanced applications such as human-machine interfaces and soft robotics. However, conventional hydrogels suffer from fracture toughness-stiffness conflict and fatigue threshold-stiffness conflict, limiting their applicability. Simultaneously enhancing the fracture toughness, fatigue threshold, and stiffness of hydrogels, especially within a homogeneous single network structure, has proven to be a formidable challenge. In this work, we overcome this challenge through the design of a loosely cross-linked hydrogel with slight dehydration. Experimental results reveal that the slightly-dehydrated, loosely cross-linked polyacrylamide hydrogel, with an original/current water content of 87%/70%, exhibits improved mechanical properties, which is primarily attributed to the synergy between the long-chain structure and the dense dehydration-induced entanglements. Importantly, the creation of these microstructures does not require intricate design or processing. This simple approach holds significant potential for hydrogel applications where excellent anti-fracture and fatigue-resistant properties are necessary.

Investigation of four nickel titanium endodontic instruments, with cyclic fatigue resistance, scanning electron microscopy, and energy dispersive x-ray spectroscopy.

The aim of this study was to compare of four different nickel-titanium (Ni-Ti) endodontic files and evaluate in terms of cyclic fatigue resistance and metallurgical properties. Four different type Ni-Ti root canal files Protaper Next X2 (PTN) (Dentsply Maillefer, Ballaigues, Switzerland), One Curve (OC) #25.06 (Micro Mega, Besancon, France), EndoPlus Flex Plus Gold X2 (EPG) (Turkuaz Dental, Denizli, Turkey), and EndoPlus Flex Plus Blue #25.06 (EPB) (Turkuaz Dental, Denizli, Turkey) files were tested for cyclic fatigue resistance (n = 20). During experiments artificial zirconia block canal was used. The artificial canal designed with curvature 60° and 5-mm radius. The number of cyclic to fracture (NCF) was noted. Fractured length (FL) parts of Ni-Ti files were recorded to assessment of fracture volumetric point. All fractured surfaces of Ni-Ti files were assessed by scanning electron microscope (SEM) to confirm the type of fractures. Descriptive evaluation become accomplished for the fundamental composition of units with the aid of using energy-dispersive x-ray spectroscopy (EDX). NCF data were evaluated via Bonferroni test with post hoc multiple comparison method. OC showed the highest NCF values (p < .05). The standardization of the study was confirmed as the FL of files was statistically similar in length (p > .05). SEM analysis confirmed that all scanned samples were fractured due to cyclic fatigue. EDX analysis confirmed that EPB established the poorest Ni content file. RESEARCH HIGHLIGHTS: The cyclic fatigue-related failure of One Curve was significantly more resistant than Protaper Next and EndoPlus files. Scanning electron microscopy images showed that One Curve and Protaper Next have round tips Energy dispersive x-ray spectroscopy showed that all four endodontic instruments mainly have Nickel and Titanium elements.

Physically Crosslinked Poly(methacrylic acid)/Gelatin Hydrogels with Excellent Fatigue Resistance and Shape Memory Properties.

Hydrogels endure various dynamic stresses, demanding robust mechanical properties. Despite significant advancements, matching hydrogels' strength to biological tissues and plastics is often challenging without applying potentially harmful crosslinkers. Using hydrogen bonds as sacrificial bonds offers a promising strategy to produce tough, versatile hydrogels for biomedical and industrial applications. Poly(methacrylic acid) (PMA)/gelatin hydrogels were synthesized by thermally induced free-radical polymerization and crosslinked only by physical bonds, without adding any chemical crosslinker. The addition of gelatin increased the formation of hydrophobic domains in the structure of the hydrogels, which acted as permanent crosslinking points. The increase in PMA and gelatin contents generally led to a lower equilibrium water content (WC), higher thermal stability and better mechanical properties. The values of tensile strength and toughness reached up to 1.44 ± 0.17 MPa and 4.91 ± 0.51 MJ m-3, respectively, while the compressive modulus and strength reached up to 0.75 ± 0.06 MPa and 24.81 ± 5.85 MPa, respectively, with the WC being higher than 50 wt.%. The obtained values for compressive mechanical properties are comparable with super-strong hydrogels reported in the literature. In addition, hydrogels exhibited excellent fatigue resistance and biocompatibility, as well as great shape memory properties, which make them prominent candidates for a wide range of biomedical applications.