Dynamic Mechanical Analysis Results Research Articles

Preparation and Properties of Epoxy Adhesives with Fast Curing at Room Temperature and Low-Temperature Resistance.

Developing a highly efficient multifunctional epoxy adhesive is still an enormous challenge, which can rapidly cure at room temperature and has excellent low-temperature resistance performance and is crucial for the epoxy adhesive and electrical sealing fields during severe cold seasons. Herein, diglycidyl phthalate (DP) was synthesized with phthalic anhydride (PA) and epichlorohydrin (ECH) to enhance the curing rate and low-temperature resistance of bisphenol A diglycidyl ether (DGEBA) adhesive. The modified DP/DGEBA adhesives were systematically analyzed by gel time, mechanical properties, and aging resistance (time, temperature, and dry/wet treatment). The results showed that DP with highly active ester groups significantly accelerates the curing speed of DP/DGEBA. DP's rigid aromatic ring-benzene ring and flexible group-ester group gave the adhesive better low-temperature resistance. When the addition of DP was 10 wt % (based on the mass of DGEBA), the gel time of DP/DGEBA epoxy adhesives was reduced by 58 min compared to unmodified DGEBA epoxy adhesive, and after aging at low temperature (-20 °C) for 7 days, the tensile shear strengths of polyvinyl chloride (PVC) and aluminum plate increased by 76.2 and 80.6%, respectively. The results of non-isothermal curing kinetics and dynamic mechanical analysis suggested that when the amount of DP was 10 wt %, the reaction activation energy of DP/DGEBA epoxy adhesive decreased by 4.0%, and the cross-linking density increased by 8.9%. Moreover, the toughness of the modified adhesive was also improved. This study opens up a feasible way for the development of a low temperature-resistant epoxy adhesive cured rapidly at room temperature in practical application.

Spectral analysis and dynamic properties of polyurethanes dyed with rhodamine 6G and rhodamine B as matrices of a solid-state laser element

A comparison was carried out of the nature of intermolecular interactions, elastic properties and gas permeability of the crosslinked polyurethanes doped with xanthene dyes and original polyurethane using IR spectroscopy, dynamic mechanical analysis (DMA) and electron paramagnetic resonance (EPR). The introduced dye can be considered as useful microimpurity which, however, can affect the efficiency of the laser. In IR spectra of polyurethanes the complex band of stretching vibrations of C=O groups is sensitive to the nature of intermolecular interaction of urethane groups. From the analysis of that band it is shown that in the presence of dyes, self-association of urethane groups within the hard segment predominates and the interaction of urethane groups with the oligoether component decreases, which can contribute to increasing the mobility of the flexible component. A decrease in the dynamic storage modulus (E’) and a decrease in the glass transition temperature (Tc) of polyurethanes in the presence of dyes is shown by the DMA method. The results of both DMA and IR spectroscopy indicate a greater increase in the mobility of the elastic component with the introduction of the rhodamine B dye, covalently bound to the polyurethane chain. According to nitroxyl paramagnetic probe data the introduction of both rhodamine B and rhodamine 6G dyes into polyurethanes increases their permeability to vapors of low-molecular weight compounds, but rhodamine 6G has a more prominent effect on this characteristic. This is consistent with DMA data indicating a greater increase in the Mc value in the presence of rhodamine 6G in polyurethane. The obtained results make it possible to determine the optimal composition of the active laser medium and are important in assessing the radiation resistance of the polymer matrix. Its increase is facilitated by a decrease in the storage modulus and an increase in the gas permeability of the polymer, leading to a decrease in pressure in the area of local heating.

Bio-spiroacetal polyurethane covalent adaptive network with close-loop recycling, self-healing and reprocessability

Conventional polyurethanes from non-renewable resources have been widely used for their excellent mechanical properties and thermal stability, which are difficult to be reprocessed and recycled due to the permanent crosslinked networks. In this study, dynamic acetal bonds were synthesized using bio-based vanillin and then embedded in polymer with castor oil to construct bio-based recyclable polyurethane. The ratio of castor oil to bio-spiroacetal diols was varied to control the thermodynamics and mechanical performance of bio-based polyurethanes. Experimental results of dynamic mechanical analysis, differential scanning calorimetry, tensile test and stress relaxation test suggested that a decrease in the content of acetal diols as a hard segment, led to a decrease in the glass transition temperature and tensile strength. Additionally, the activation energy initially increased and then decreased. The reversibility of the acetal structure endowed green polyurethane materials with the ability of reprocessing, self-repairing and closed-loop recycling.

Structuring restricted amorphous molecular chains in the reinforced cellulose film by uniaxial stretching

The construction of the preferred orientation structure by stretching is an efficient strategy to fabricate high-performance cellulose film and it is still an open issue whether crystalline structure or amorphous molecular chain is the key factor in determining the enhanced mechanical performance. Herein, uniaxial stretching with constant width followed by drying in a stretching state was carried out to cellulose hydrogels with physical and chemical double cross-linking networks, achieving high-performance regenerated cellulose films (RCFs) with an impressive tensile strength of 154.5 MPa and an elastic modulus of 5.4 GPa. The hierarchical structure of RCFs during uniaxial stretching and drying was systematically characterized from micro- to nanoscale, including microscopic morphology, crystalline structure as well as relaxation behavior at a molecular level. The two-dimensional correlation spectra of dynamic mechanical analysis and Havriliak-Negami fitting results verified that the enhanced mechanical properties of RCFs were mainly attributed to the stretch-induced tight packing and restricted relaxation of amorphous molecular chains. The new insight concerning the contribution of molecular chains in the amorphous region to the enhancement of mechanical performance for RCFs is expected to provide valuable guidance for designing and fabricating high-performance eco-friendly cellulose-based films.

Thermophysical Properties of Composite Metal-Filled Copolymers of Polyvinylpyrrolidone

The effect of the presence of finely dispersed metal fillers of various natures (Zn, Co, Ni) on the thermophysical characteristics (Vick heat resistance, glass transition temperature) of polyvinylpyrrolidone block copolymers with 2-hydroxyethylmethacrylate was studied. It was found that the heat resistance of the obtained composites significantly exceeds the heat resistance of unfilled copolymers and is in the range of 360-395K, depending on the nature and content of the metal filler. The change in heat resistance correlates with the change in glass transition temperature, which was evaluated according to the results of thermomechanical and dynamic mechanical thermal analyses. The results of this work are an additional source to characterize the structure of metal-filled copolymers: they confirm the participation of metal filler particles in the formation of the nodes of the copolymer spatial network, and also prove the formation of a different polymer network structure in the interfacial layer on the surface of the metal particle and in the polymer volume.

The impacts of CaCO3 deposition in natural wood on its viscoelastic properties

In this study, we discuss the methods used for depositing calcium carbonate (CaCO3) and the resulting 2D and 3D particle distributions of CaCO3 in two types of wood, which were quantified using scanning electron microscopy (SEM) and X-ray computed tomography (CT). We also present the results of dynamic mechanical analysis (DMA), which was used to measure the impact of CaCO3 deposition on the viscoelastic properties of the wood. X-ray CT scanning showed that CaCO3 deposits inside the wood scaffold with increased amounts as the deposition cycles were iterated. However, DMA results did not indicate significant improvement in storage moduli (E′) of CaCO3 deposited wood. SEM images revealed that the particles did not fill all the voids to provide stress transfer between the wood scaffold and the particles, indicating a lack of composite action between the wood and CaCO3 components. To address this issue, we hypothesized that heat-pressing would lead to a mechanical bond between the particles and the matrix. After heat-pressing, DMA results showed a dramatic increase in E′ not only in CaCO3 deposited wood samples but also in control wood samples. In other words, the densification of the structure led to significant increases in E′, primarily due to densification, while the impact of the presence of CaCO3 particles was minimal. This is mainly because the volume fraction of the deposited CaCO3 particles is small as compared to the total volume of the composite.

Temperature-Controlled Chain Dynamics in Polyimide Doped with CoCl2 Probed Using Dynamic Mechanical Analysis.

Cobalt(II) chloride (CoCl2) being in the vicinity of polyimide chains entails modifications in terms of the molecular dynamics, which are mainly governed by the possible presence of amic acid residual groups, by the transition-metal-type characteristics of cobalt and by the CoCl2 content. Polyimide was synthesized using poly(amic acid) according to the reaction of 2,2'-bis(3,4-dicarboxylphenyl)hexafluoropropane dianhydride (6FDA) with 3,3'-dimethyl-4,4'-diaminodiphenylmethane (MMDA) in N,N-dimethylacetamide. CoCl2 was added before the thermal imidization of the poly(amic acid). An experimental approach was designed to establish the interaction between the polyimide and CoCl2 and whether the interaction depends on the quantity of the salt. Evidence for the existence of residual amic acid groups was obtained using second derivative Fourier Transform Infrared Spectroscopy (FTIR) and with the help of 2D correlation spectroscopy (2D-COS). Moreover, FTIR, along with X-ray photoelectron spectroscopy (XPS), revealed the interaction between the polymer and CoCl2, primarily in the form of Co(II)-N coordinated bonds. Nevertheless, the coordination of cobalt with suitable atoms from the amic acid groups is not precluded. The results of dynamic mechanical analysis (DMA) featured a specific relaxation assigned to the presence of CoCl2 in the polymeric film and demonstrated that its (non)reinforcing effect depends on its content in the polyimide.

Molecular Interaction Study in the Binary Liquid Mixture of PEO and DMF by Ultrasonic Technique

The non‐destructive ultrasonic technique is a great employ for knowing the solute–solvent interaction in the polymer blend. By the ultrasonic velocity and attenuation evaluation, the visco‐elastic behaviors of the polymer solution have been assessed and compared with the results of conventional dynamic mechanical analysis. In the present research work, a comprehensive ultrasonic investigation of molecular interaction in a polymeric mixture of Poly (ethylene oxide) PEO and dimethyformamide (DMF) at 333 K has been executed by using the information provided by the literature. For this purpose, ultrasonic waves of two different frequencies such as 2 and 5 MHz have been implemented. Several acoustical parameters such as adiabatic compressibility, acoustic impedance, relaxation time, and ultrasonic attenuation coefficient (𝛼/𝑓2) are explored. Thermodynamic parameters like relative association and intermolecular free path length are also estimated. The evaluated values have been associated with the previous experimental results. The non‐ideal approach of the solution is analyzed and discussed in detail.

Evaluation of Starch-Garlic Husk Polymeric Composites through Mechanical, Thermal, and Thermo-Mechanical Tests.

The present work evaluates the influence of different properties of composite materials from natural sources. Films were prepared using the evaporative casting technique from corn starch reinforced with a waste material such as garlic husk (GH), using glycerin as a plasticizer. The results of the syntheses carried out demonstrated the synergy between these materials. In the morphological analysis, the compatibility and adequate dispersion of the reinforcer in the matrix were confirmed. Using Fourier transform infrared spectroscopy (FTIR), the interaction and formation of bonds between the matrix and the reinforcer were confirmed by the presence of some signals such as S-S and C-S. Similarly, thermogravimetric analysis (TGA) revealed that even at low concentrations, GH can slightly increase the decomposition temperature. Finally, from the results of dynamic mechanical analysis (DMA), it was possible to identify that the storage modulus increases significantly, up to 115%, compared to pure starch, especially at low concentrations of the reinforcer.

Effect of microstructure tuning by rapid heat cycle molding on the photodegradation behavior of isotactic polypropylene

AbstractRapid heat cycling molding (RHCM) is an injection molding technique that improves the product quality of isotactic polypropylene (iPP) by tuning the microstructure, but its effect on the photodegradation stability remains to be investigated. In this work, the effect of RHCM tuned microstructure on the photodegradation behavior of iPP was investigated and compared with conventional injection molding (CIM). Differential scanning calorimetry (DSC), x‐ray diffraction (XRD), Fourier transform infrared spectrometer (FTIR), atomic force microscopy (AFM), and shore durometer (D scale) were used to examine the photodegradation behavior of iPP samples. The results showed that RHCM increased the crystallinity, crystal size, and β‐crystal content of iPP samples. With the increase of photodegradation time, iPP samples injected with RHCM showed higher stability in terms of microstructure and surface quality. The relative changes in CI and Ra of RHCM90 were reduced by 48% and 40% after 800 h of UV irradiation, respectively. In addition, the combined results of dynamic mechanical analysis (DMA) and UV–visible absorption spectrum showed that RHCM promoted the development of crystalline structure and reduced the mobility of the surface chain segments as well as UV absorption coefficient. These combined effects contributed positively to its photodegradation stability.

Biomass- and Carbon Dioxide-Derived Polyurethane Networks for Thermal Interface Material Applications.

Recent environmental concerns have increased demand for renewable polymers and sustainable green resource usage, such as biomass-derived components and carbon dioxide (CO2). Herein, we present crosslinked polyurethanes (CPUs) fabricated from CO2- and biomass-derived monomers via a facile solvent-free ball milling process. Furan-containing bis(cyclic carbonate)s were synthesized through CO2 fixation and further transformed to tetraols, denoted FCTs, by aminolysis and utilized in CPU synthesis. Highly dispersed polyurethane-based hybrid composites (CPU-Ag) were also manufactured using a similar ball milling process. Due to the malleability of the CPU matrix, enabled by transcarbamoylation (dynamic covalent chemistry), CPU-based composites are expected to present very low interfacial thermal resistance between the heat sink and heat source. The characteristics of the dynamic covalent bond (i.e., urethane exchange reaction) were confirmed by the results of dynamic mechanical thermal analysis and stress relaxation analysis. Importantly, the high thermal conductivity of the CPU-based hybrid material was confirmed using laser flash analysis (up to 51.1 W/m·K). Our mechanochemical approach enables the facile preparation of sustainable polymers and hybrid composites for functional application.

The synthesis of an epoxy-terminated hyperbranched polysiloxane toughener and its application at low temperature

To improve the low-temperature toughness of epoxy resins, in this study, an epoxy-terminated hyperbranched polysiloxane (EPTS-12) was synthesized and introduced into the epoxy resin as a toughener. The structure of EPTS-12 was characterized by Fourier transform infrared spectroscopy (FT-IR) and nuclear magnetic resonance (1H NMR), and the fractured surfaces of the modified resins were observed by a scanning electron microscope (SEM). With the content of EPTS-12 at 5 wt%, under room temperature (RT) and − 72 °C, the maximum values of elongation at break were 14.19% and 16.06%, increasing by 35.66% and 74.19% respectively. The test results of dynamic mechanical analysis (DMA) also showed that the toughness of the modified epoxy resins was improved. The SEM images of the fractured surfaces of the modified resins were used to investigate the toughening mechanism of the toughener (EPTS-12). With the virtue of a simple synthesis process, low cost, and good reproducibility, this toughener can further expand the application of epoxy resins.

The synthesis of a secondary branched epoxy‐modified silicone resin and its application at low temperature

AbstractTo enhance the fracture toughness of epoxy resin at low temperature, a secondary branched epoxy‐terminated silicone resin (ESR‐6) was synthesized and incorporated into bisphenol A epoxy resin at different contents. The structure of ESR‐6 was characterized by Fourier transform infrared spectroscopy and nuclear magnetic resonance (1H NMR), and the fracture surface of the composites was observed by scanning electron microscope (SEM) and atomic force microscopy. At room temperature and − 70°C, the maximum values of elongation at break were 15.78% and 12.55% with 10 wt% ESR. Compared with those of neat epoxy resin, the values of elongation at break of the composite were increased by 50.86% and 36.12%. The results of dynamic mechanical analysis also showed that the toughness of the modified resin had been improved. The SEM images of the fracture surfaces suggested that the fracture mode of the modified resin changed from brittle one to plastic one because of the addition of ESR‐6, which further confirmed the toughening effect of ESR‐6. These research results may provide a new strategy for enhancing the low‐temperature toughness of epoxy resins.

Experimental study on mechanical, damping and corrosion properties of Inconel 718 hard-faced stainless steel 304 using cold metal transfer

Cold Metal Transfer process is used to hard-face the Inconel 718 alloy onto the Stainless Steel 304 material. The optimized parameters from the Bead on Plate trials were determined as a wire feed rate of 7 m/min, deposition speed of 15 cm/min, welding current, and voltage of 175 A and 14.9 V, respectively. Hard-facing is carried out with the sinewave weaving technique along 30 % of overlapping beads. The analysis is focused on revealing the hard-faced specimens' microstructural, mechanical, and electrochemical corrosion properties. The hard-face layer exhibits grains of mixed modes, including columnar, cellular, and fine equiaxed grains. The increased heat transfer disintegrates grain formation and reduces secondary arm spacing development. SEM-Elemental mapping shows the reduction of Niobium (3.61 %) segregation and laves formation. The overlay layer has a maximum hardness of 343.1 HV0.5 over the base substrate with 204 HV0.5. The impact test reveals the hard-faced layer absorbs more energy (26.3 %) than the substrate. Dynamic Mechanical Analysis results indicate overlay layer enhancing damping properties. The electrochemical corrosion test findings suggest that the hard-faced layer's high corrosion potential (Ecorr = 8.533 mV) corresponds to a high corrosion resistance. Phase and intermetallic formations, distribution of elements, fractured and corrosive surface morphologies are analyzed using SEM, EDX, and elemental mapping results.

Polyurea-Graphene Nanocomposites-The Influence of Hard-Segment Content and Nanoparticle Loading on Mechanical Properties.

Polyurethane and polyurea-based adhesives are widely used in various applications, from automotive to electronics and medical applications. The adhesive performance depends strongly on its composition, and developing the formulation-structure-property relationship is crucial to making better products. Here, we investigate the dependence of the linear viscoelastic properties of polyurea nanocomposites, with an IPDI-based polyurea (PUa) matrix and exfoliated graphene nanoplatelet (xGnP) fillers, on the hard-segment weight fraction (HSWF) and the xGnP loading. We characterize the material using scanning electron microscopy (SEM) and dynamic mechanical analysis (DMA). It is found that changing the HSWF leads to a significant variation in the stiffness of the material, from about 10 MPa for 20% HSWF to about 100 MPa for 30% HSWF and about 250 MPa for the 40% HSWF polymer (as measured by the tensile storage modulus at room temperature). The effect of the xGNP loading was significantly more limited and was generally within experimental error, except for the 20% HSWF material, where the xGNP addition led to about an 80% increase in stiffness. To correctly interpret the DMA results, we developed a new physics-based rheological model for the description of the storage and loss moduli. The model is based on the fractional calculus approach and successfully describes the material rheology in a broad range of temperatures (-70 °C-+70 °C) and frequencies (0.1-100 s-1), using only six physically meaningful fitting parameters for each material. The results provide guidance for the development of nanocomposite PUa-based materials.

Investigation of Thermal, Mechanical and Shape Memory Properties of 3D-Printed Functionally Graded Nanocomposite Materials.

In this study, a 3D-printed photocurable resin was developed by incorporating graphene nanoplatelets functionalised with melamine to investigate the thermal, mechanical, fracture and shape memory behaviours. The objective of this work was to produce a printed functionally graded nanocomposite material that has a smart temperature-responsive structure; presents good thermal stability, strength and fracture toughness; and can demonstrate shape-changing motions, such as sequential transformations, over time. The functionalised graphene nanoplatelets were examined via thermogravimetric analysis, Fourier transform infrared spectroscopy, Raman spectroscopy and ultraviolet-visible spectroscopy. Thermogravimetric analysis showed that the degradation temperature of the nanocomposite containing 0.1 wt% of functionalised graphene nanoplatelets at the weight loss of 5% was 304 °C, greater than that of the neat one by 29%. Dynamic mechanical analysis results showed property enhancements of the storage modulus and glass transition temperature. Fracture toughness, tensile strength and impact resistance were improved by 18%, 35% and 78%, respectively. The shape memory tests were performed to obtain the temperature-time recovery behaviour of the 3D-printed structures. The addition of functionalised graphene nanoplatelets demonstrated an enhancement in the shape recovery ratios. Generally, the five subsequent cycles were notably stable with a high recovery ratio of 97-100% for the flat shape and circular shape of the M-GNP specimens. On the other hand, these values were between 91% and 94% for the corresponding neat specimens.

Phase morphology, rheological behavior and mechanical properties of supertough biobased poly(lactic acid) reactive ternary blends

Poly(lactic acid) (PLA) is one of the most promising bio-based polyester with great potential to replace for the petroleum-based polymers, which can significantly reduce greenhouse gas emissions. However, the inherent brittleness of PLA seriously restricts its broad applications. Herein, PLA/poly(ε-caprolactone) (PCL)/ethylene methyl acrylate-glycidyl methacrylate (EMA-GMA) ternary blends with different phase structures were prepared through reactive blending. The reactions between the epoxy groups of EMA-GMA and the carboxyl and hydroxyl end groups of PLA and PCL and were evidenced from the Fourier transform infrared spectroscopy, dynamic mechanical analysis and rheological results. The atomic force microscopy (AFM) images clearly revealed the formation of stack structure of the PCL and EMA-GMA minor phases in PLA/PCL/EMA-GMA (80/15/5) blend, and core-shell particle structures in PLA/PCL/EMA-GMA (80/10/10) and (80/5/15) blends. In terms of elongation at break and impact toughness, PLA/PCL/EMA-GMA (80/5/15) blend presents the best properties among all the compositions. Moreover, it also behaved excellent stiffness-toughness balance. The toughening mechanism can be ascribed to the formation of core-shell structure and the existence of interfacial adhesion in the ternary blends. This work can provide guide for the preparation and design of PLA-based partially renewable supertough materials that can compete with conventional petro-derived plastics.

Synthesis and characterization of low dielectric constant polybenzoxazines with different fluorine contents

AbstractThe rapid development of integrated circuits puts forward higher requirements for low dielectric constant polymers. In this study, two fluorinated benzoxazine monomers, bis‐(3,4‐dihydro‐3‐(4‐fluoro‐3‐(trifluoromethyl)phenyl)‐2H‐1,3‐benzoxazine)isopropane (BA‐ftfa) and bis‐(3,4‐dihydro‐3‐(4‐fluoro‐3‐(trifluoromethyl)phenyl)‐2H‐1,3‐benzoxazine)isoperfluoropropane (BAF‐ftfa), were successfully synthesized. Differential scanning calorimeter (DSC) was used to monitor the thermal curing behaviors of the monomers and their mixtures. Five groups of polybenzoxazine samples with different fluorine content (25% ~ 35%) were obtained by copolymerizing the two monomers with different mass ratios. The effects of fluorine content on dielectric properties were investigated and the results show that PBAF‐ftfa with the highest fluorine content has the lowest dielectric constant of 2.53 at 1 MHz. Furthermore, the results of thermogravimetric analysis (TGA) and dynamic mechanical analysis (DMA) show that all polymers possess excellent thermal stability and exhibit high glass transition temperatures over than 180°C.

Design, fabrication and characterization of dynamic covalent polymer networks containing reversible Diels-Alder adducts derived from vegetable oil and furfural

The exploration of novel bio-based functional polymers has high application value and confirms to sustainable development strategies following the increasing shortage of fossil resources. In this research, several different recyclable bio-based dynamic covalent polymer networks (DCPNs) containing dynamic Diels-Alder bonds from vegetable oil and furan were designed and fabricated via a simple preparation process. The reprocessability, shape memory, molecular structures, thermal properties and mechanical properties of the DCPNs were all investigated. 1H nuclear magnetic resonance (1H-NMR) and Fourier transform infrared spectroscopy (FTIR) analysises demonstrated the target reactive products were all successfully synthesized. Variable-temperature FTIR and differential scanning calorimetry revealed the changing rule of dynamic Diels-Alder bond molecular structures with temperature. The DCPNs possess controllable tensile properties including superior ductility and certain rigidity via adjusting fatty chain component, which is in accordance with the result of dynamic mechanical analysis. Thermal gravimetric analysis demonstrated the DCPNs had excellent thermostability, and the main peak decomposition temperatures were all above 460 °C. The nature of the dynamic Diels-Alder bonds could make shattered DCPNs be reprocessed multiple times under relatively mild conditions. The DCPNs displayed certain shape memory properties, and the shape fixation and recovery ratio at the last two cycles were kept above 95.53% and 84.58%, respectively. This work will help with the development on this kind of bio-based polymers containing dynamic Diels-Alder covalent bonds.

Nanoscale dynamic mechanical analysis on interfaces of biological composites

Biological composites incorporate structural arrays of rigid-elastic reinforcements made of minerals or crystalline biopolymers, which are connected by thin, compliant, and viscoelastic macromolecular matrix material. The near-interface regions of these biological composites grant them energy dissipation capabilities against dynamic mechanical loadings, which promote various biomechanical functions such as impact adsorption, fracture toughness, and mechanical signal filtering. Here, we employ theoretical modeling and finite-element simulations to analyze the mechanical response of the near-interface in biological composites to nanoscale dynamic mechanical analysis (DMA). We identified the dominating load-bearing mechanisms of the near-interface region and employed these insights to introduce simple semi-empirical formulations for approaching the mechanical properties (storage and loss moduli) of the biological composite from the nanoscale DMA results. Our analysis paves the way for the nanomechanical characterization of biological composites in diverse natural materials systems, which can also be employed for bioinspired and biomedical configurations.