Bulk Modulus Research Articles

Compressive and Tensile Behavior of High-Ductility Alkali-Activated Composites with Polyethylene Terephthalate Powder

Researchers have been engaged in the study of high-ductility concrete (HDC) due to its excellent ductility and cracking control ability. This study combines the concepts of HDC and alkali-activated composites (AAC) to develop high-ductility alkali-activated composites (HDAAC) using polyethylene terephthalate (PET) powder. Experimental investigations were conducted to assess the compressive and tensile properties of HDAAC, focusing on the impact of varying PET powder content (0%, 15%, 30%, and 45%) and fly ash/slag ratios (FA/GGBS, 6:4, 7:3, and 8:2). The results indicated that the compressive strength of HDAAC ranged from approximately 30 MPa to about 100 MPa, with the specimens maintaining good integrity after axial compression failure due to the bridging action of PE fibers. The replacement of quartz powder (QP) with PET powder slightly decreased the compressive strength and elastic modulus of HDAAC, albeit mitigating its brittleness under compression. An increase in GGBS content enhanced the compressive strength and elastic modulus of HDAAC due to the increased formation of the C-A-S-H reaction products, leading to reduced porosity and a denser microstructure. Under axial tension, HDAAC exhibited typical multiple-cracking behavior with significant pseudo-strain hardening. Increases in the PET content and FA/GGBS ratio resulted in finer cracks, indicating excellent crack control and deformation capabilities. The initial cracking strength, tensile strength, and ultimate tensile strain ranged from 3.0 MPa to 4.6 MPa, 4.2 MPa to 8.2 MPa, and 4.1% to 7.2%, respectively. Despite a decrease in the initial cracking strength and tensile strength with higher PET content, the ultimate tensile strain of HDAAC slightly increased. Observations under a scanning electron microscope revealed a distinct interfacial transition zone near the PET powder, leading to poor bonding with the alkali-activated matrix. In contrast, QP dissolved on the surface in highly alkaline environments, forming better interface properties. These variations in interface properties can be used to interpret the variations in the mechanical performance of HDAAC.

An experimental and numerical investigation into compressive failure of pyramidal lattice sandwich structures fabricated using stereolithography technology

AbstractThe pyramid lattice sandwich structure, characterized by high load‐bearing capacity, lightweight nature, and fully open internal space, is considered an extremely promising super‐strong structure. Stereolithography technology was utilized to achieve the monolithic formation of single‐layer multi‐cell pyramidal lattice sandwich structures. Quasi‐static compression tests and finite element simulations were conducted to characterize the compressive properties and failure modes. Results indicate that the compressive strength, compressive modulus, specific strength, and specific stiffness of the single‐layer multi‐cell pyramidal lattice sandwich structure increase as the relative density increases. Moreover, fracture failure was observed in the structures with various relative densities. Additionally, the compressive failure of multi‐layer density gradient pyramidal lattice sandwich structures was investigated. Experimental and numerical findings indicate that the optimal density gradient scheme for the ZCMLG structure is I‐III‐II, resulting in a peak compression force that is 342.14% and 288.55% higher than that of the ZAMLG and ZBMLG structures, respectively.

Elastic behaviour of bamboo at nano- and microscale

This paper presents an anatomy-based numerical multiscale approach for modelling the mechanical behaviour of Moso bamboo, addressing limitations in previous research where the intricate microstructure was often simplified. The mechanical response of bamboo culms is predicted at the nano and microscale considering the orthotropic behaviour of cellulose microfibrils in different layers of tissues, deviating from conventional isotropic assumptions. Through nano and microscale finite element models, the impact of chemical composition and microfibril angle on elastic properties of different layers of the fibre and parenchyma cells are explored at two different levels of moisture content. At low moisture content, fibres within vascular bundles exhibit significantly higher longitudinal and transverse elastic moduli compared to parenchyma cells. When the moisture content is high, the properties of the fibre and parenchyma cells are less different. Anisotropic behaviour at the nanoscale contributes to a more accurate prediction of the mechanical properties of bamboo culms at the microscale, particularly in the transverse direction in moist conditions. This study lays the groundwork for forthcoming research in modelling the mechanical behaviour of bamboo culm at meso and macroscales.

Speed of sound measurement and mapping in transparent materials by impulsive stimulated Brillouin microscopy

Impulsive stimulated Brillouin scattering (ISBS) is a variant of stimulated Brillouin scattering, which can overcome the shortcomings of the long acquisition time of traditional Brillouin microscopy. We introduce the difference between ISBS and other Brillouin microscopies in calculating longitudinal modulus. The Brillouin frequency shift obtained by ISBS is only related to the system parameters and the speed of sound (SOS) in the sample, not to the refractive index. Non-contact SOS measurement of homogeneous samples is an important application of Brillouin scattering, used in the early study of Brillouin spectroscopy and the mechanical properties of liquids. However, the measurement requires prior knowledge of the sample refractive index, which limits the measurement of the unknown refractive index sample. Here, we propose a method to measure the SOS based on ISBS, which in principle avoids the need for refractive index parameters. The SOS of several liquids are measured and compared with the standard values. The mean relative standard deviation is 1.13%. Moreover, we measure the SOS of a mixture of ethanol and water to demonstrate an application of measuring SOS without refractive index information. We also demonstrate the high spatial resolution of ISBS with a methanol-filled PDMS sample.

Structural stability, mechanical, and thermodynamic properties under pressure of B2-type CuM (M = Be, Al, and Zn) alloys: a DFT investigation

In this work, we systematically examined the structural stability, mechanical properties, and thermodynamic behavior of B2-type CuBe alloy, and compared the results with isostructural Cu-based alloys (CuAl and CuZn) by employing first-principles calculations in the pressure range of −22 to 100 GPa. This study revealed the stable existence of CuBe alloy at low-density expansion states (e.g. ∼ −20 GPa), indicating its superior structural stability compared to CuAl and CuZn. The pressure dependence of properties such as cell parameter a (a/a 0) and density ρ (ρ/ρ 0), elastic parameters (elastic constants C ij , bulk modulus B, shear modulus G, and Young's modulus E), deduced parameters (B/G ratio, Poisson's ratio ν, Vickers hardness, sound velocity, and Debye termperature ΘD), and thermodynamic parameters (free energy F, entropy S, and heat capacity C v) were investigated. All CuM (M = Be, Al, and Zn) alloys had more difficulty undergoing uniaxial stress than shear stress. External pressure reduced the ductility of the CuBe alloy, while excess pressure (P > 50 GPa) resulted in increased ductility, which was similar to CuAl but different from CuZn. The hardness and ΘD values demonstrated consistent variation corresponding to the ductility changes. Thermodynamic parameters were minimally affected by pressure, and the stronger interactions led to greater F in the CuBe alloy. These findings offer confidence for the future design of ordered Cu-Be alloys with exceptional properties.

Mechanical properties of recycled aggregate concrete containing brick particles

To investigate the mechanical properties of recycled aggregate concrete containing brick particles(RACB), compressive strength tests were conducted on RACBs with different water cement ratios and recycled fine aggregate substitution rates. The changes in compressive strength, elastic modulus, and peak strain of RACB with recycled fine aggregate substitution rates were analyzed, and a stress–strain equation was established. A damage model was established using ultrasonic nondestructive testing technology to reveal the damage mechanism of RACB. Results show that the basic mechanical properties of RACB reach the best when the replacement rate of recycled fine aggregate (r) is 30%. The model parameter a of the stress–strain curve equation is consistent with the change rule of elastic modulus with r. The model parameter b has a quadratic function relationship with r, reflecting the brittleness of RACB. The initial damage of RACB is relatively large, and the cracks penetrate the recycled coarse aggregate, and lead to specimen failure.

Image‐based inertial impact test for viscoelastic constitutive identification: A digital replica for error quantification

AbstractPolymers find widespread use in applications where they are subjected to impact loading. Therefore, understanding the time dependence of their mechanical response is critical to the design of structures subjected to these high strain rate environments. However, characterising these materials on microsecond time scales has proven challenging. Traditional experimental techniques rely on satisfying a number of limiting assumptions and typically do not provide direct measurements of the material parameters. Here, we propose a novel implementation of the image‐based inertial impact (IBII) test to extract viscoelastic constitutive parameters on these microsecond time scales using the stress gauge implementation of the virtual fields method. We validate the experiment using a digital replica approach in which the constitutive parameters are first extracted on a finite element model of an IBII test on a viscoelastic material. The finite element data are then used to synthetically deform computer‐generated grid images, which are then polluted with grey‐level noise to simulate the images that would be captured in a real‐life experiment. These images are processed identically to a physical experiment, and the identification is repeated using the full‐field displacements extracted from the computer‐generated images to determine the ideal processing parameters. Parameter identification was found to strongly depend on the processing parameters used to extract the kinematic fields from full‐field images, emphasising the need for computational validation before attempting a physical experiment to extract constitutive parameters. The IBII experimental method was found to be capable of simultaneously identifying the bulk modulus and the shear modulus along with their associated time constant.

Revisiting thermodynamics in (LiF, NaF, KF, CrF2)–CrF3 by first-principles calculations and CALPHAD modeling

The thermodynamic description of the (LiF, NaF, KF, CrF2)–CrF3 systems has been revisited, aiming for a better understanding of the effects of Cr on the FLiNaK molten salt. First-principles calculations based on density functional theory (DFT) were performed to determine the electronic and structural properties of each compound, including the formation enthalpy, volume, and bulk modulus. DFT-based phonon calculations were carried out to determine the thermodynamic properties of compounds, for example, enthalpy, entropy, and heat capacity as functions of temperature. Phonon-based thermodynamic properties show a good agreement with experimental data of binary compounds LiF, NaF, KF, CrF3, and CrF2, establishing a solid foundation to determine thermodynamic properties of ternary compounds as well as to verify results estimated by the Neumann-Kopp rule. Additionally, DFT-based ab initio molecular dynamics (AIMD) simulations were employed to predict the mixing enthalpies of liquid salts. Using DFT-based results and experimental data in the literature, the (LiF, NaF, KF, CrF2)–CrF3 system has been remodeled in terms of the CALculation of PHAse Diagrams (CALPHAD) approach using the modified quasichemical model with quadruplet approximation (MQMQA) for liquid. Calculated phase stability in the present work shows an excellent agreement with experiments, indicating the effectiveness of combining DFT-based total energy, phonon, and AIMD calculations, and CALPHAD modeling to provide the thermodynamic description in complex molten salt systems.

Physical and mechanical characteristics deterioration and crack evolution of sandy mudstone in an open-pit mine under multiple freeze–thaw cycles

In open-pit mines located in cold regions north of the 38°N latitude, there are significant freeze–thaw phenomena in slope rocks. This study conducted freeze–thaw cycle tests, considering the number of freeze–thaw cycles and the freezing temperature, on sandy mudstone commonly found in the slopes of open-pit mines. The investigation focused on the effects of freeze–thaw cycles on the physical and mechanical properties and acoustic emission (AE) characteristics of sandy mudstone. The results show that, with an increase in the number of freeze–thaw cycles and a decrease in freezing temperature, the sandy mudstone specimens exhibit nonlinear exponential changes in mass loss rate, P-wave velocity loss rate, peak strain, uniaxial compressive strength (UCS) and elastic modulus, and the amplitude of these changes gradually decreases. The stress–strain curves of specimens shift gradually from apparently brittle to plastic. Simultaneously, the microstructure changes from dense to loose, the micro surface transitions from flat to rough, and cracks and pore defects gradually develop. The peak AE ringing counts, cumulative AE ringing counts, crack initiation stress, and crack damage stress of the specimens all decrease with an increase in the number of freeze–thaw cycles and a decrease in freezing temperature. This suggests a shift from brittle failure to ductile failure. However, the ratio of crack initiation stress and crack damage stress to peak stress does not vary significantly with the number of freeze–thaw cycles and freezing temperature.

Effect of titanium dioxide as nanomaterials on mechanical and durability properties of rubberised concrete by applying RSM modelling and optimizations

The use of rubber aggregates derived from discarded rubber tyres in concrete is a pioneering approach to replacing natural aggregate (NA) and promoting sustainable building practices. Recycled aggregate in concrete serves the dual purpose of alleviating the accumulation of discarded rubber tyres on the planet and providing a more sustainable alternative to decreasing natural aggregate. Due to fact that the crumb rubber (CR) decreases the strength when used in concrete, incorporating titanium dioxide (TiO2) as a nanomaterial to counteract the decrease in strength of crumb rubber concrete is a potential solution. Response Surface Methodology was developed to generate sixteen RUNs which contains different mix design by providing two input parameters like TiO2 at 1%, 1.5%, and 2% by cement weight and CR at 10%, 20%, and 30% as substitutions for volume of sand. These mixtures underwent testing for 28 days to evaluate their mechanical, deformation, and durability properties. Moreover, the compressive strength, tensile strength, flexural strength and elastic modulus were recorded by 51.40 MPa, 4.47 MPa, 5.91 MPa, and 40.15 GPa when 1.5% TiO2 and 10% CR were added in rubberised concrete after 28 days respectively. Furthermore, the incorporation of TiO2 led to reduced drying shrinkage and sorptivity in rubberized concrete, especially with increased TiO2 content. The study highlights that TiO2 inclusion refines pore size and densifies the interface between cement matrix and aggregate in hardened rubberized concrete. This transformative effect results in rubberized concrete demonstrating a commendable compressive strength comparable to normal concrete.

Numerical simulation on cellular structure and mechanical properties of tungsten particles/polymethyl methacrylate microcellular composites

AbstractMicrocellular composites combine the advantages of composite material and microcellular material. Introducing the inclusion phase into the polymer matrix can optimize the cellular structure and improve the mechanical properties of microcellular materials. This paper focuses on rigid W particles reinforced PMMA microcellular materials, combining compression experiments and meso FE simulations to investigate the structure–property relationship of cellular structure and compressive properties for W/PMMA microcellular composites. The results indicate that W particles promote heterogeneous nucleation, reducing the cell size to 3 μm, and reinforce the PMMA matrix. W particles (10 → 60 wt%) are linearly and exponentially related to compressive modulus and compressive strength of W/PMMA microcellular composites, increased by 49.3% and 19.8%. Void porosity (71% → 48%) is quadratic related to compressive properties of W/PMMA microcellular composites, increased by 109%. Cell sizes (5 → 1 μm, especially smaller than the W particle sizes) are exponentially related to compressive properties of W/PMMA microcellular composites, increased by 38.5%. This work provides theoretical support for the regulation of cellular structure and optimization of mechanical properties of microcellular materials.

Pressure Effects on the Structural, Electronic, Elastic, Optical, and Vibrational Properties of YMg Intermetallic Compounds:A First-Principles Study

Abstract The properties of YMg in B2 structure have been comprehensively analysed using the first-principles plane-wave pseudopotential method. Specifically, the structural, electronic, elastic, vibrational, and optical properties were investigated using the generalized gradient approximation (GGA) method in the context of density functional theory. The Vienna ab initio simulation package (VASP) was utilized for these calculations. The computed lattice parameter (3.803 Å) and bulk modulus (41.33 GPa) are consistent with the earlier data on ambient pressure. The electronic band structure and energy-dependent density of states reveal the metallic nature of the titled compounds. The Born stability requirements confirmed the mechanical stability. The analysis of Pugh's and Poisson's ratios and Cauchy's pressure reveals that YMg is ductile under the pressures in consideration. According to several anisotropy indices, the compound is noticeably anisotropic both in ambient and under pressure. Our investigation includes an analysis of several fundamental mechanical parameters of the material, including the bulk modulus, the pressure derivative of the Zener anisotropy factor, Poisson's ratio, isotropic shear modulus and Young's modulus with a particular focus on their dependence on pressure. We have determined that the elastic constants obtained remain mechanically stable, satisfying the Born Stability conditions even at high pressures of up to 60 GPa. To explore the dynamic stability of YMg, we analysed the material's phonon dispersion curves. The examined compound displays stability under dynamic conditions from 0 GPa to 30 GPa, as evidenced by its positive vibration frequencies. However, this stability is not sustained under higher pressure, as the compound becomes unstable after 30 GPa to 70 GPa. 
The electronic band structure and density of states diagrams demonstrate YMg's metallic properties. At atmospheric pressure (0 GPa), the total density of states (TDOS) near the Fermi level is approximately 1.63 states/eV, with pressure application reducing DOS. The dielectric function, refractive index, and energy loss spectra are examined within the 0–20 eV energy range. YMg exhibits its highest absorption between 4 and 11 eV. The peak optical conductivity is observed around 0.78 eV (equivalent to 1589.5409 nm), while the most significant energy loss occurs at 11.90 eV, roughly corresponding to 2.8 Hz in the ultraviolet spectrum. Moreover, we extensively analyzed the material's phonon thermodynamic and optical properties, providing insights into its behavior under various conditions. The outcomes acquired at zero pressure are generally coherent with the current theoretical values.

First-principles study on the structural, elastic, electronic, optical and thermophysical properties of NaNO3 and K-doped NaNO3

Abstract The present work represents the structural, electronic, elastic, and thermophysical properties of pure and K-doped NaNO3 obtained using DFT calculations. The estimated structural properties of NaNO3 correspond well with the existing reported values. Electronic characteristics such as band structure and density of statesof pure and doped NaNO3 are analyzed where the calculated band gaps for pure and K-doped NaNO3 are found to be 3.05 eV and 2.90 eV, respectively. The Berry–phase calculations carried out on both systems showed the existence of ferroelectric polarization, where an enhanced spontaneous polarization value of 36 μC/cm2 for K-doped NaNO3, as compared to 20 μC/cm2 for intrinsic NaNO3. The thermophysical properties such as bulk modulus (B0), Debye temperature (θD), and specific heat capacity (Cv) were calculated over a wide temperature range from 0K to 800 K. The linear optical properties namely the dielectric constant, refractive index, absorption coefficient, extinction coefficient and electron energy loss function are calculated in wide energy range from 0 to 30 eV and discussed in detail.

An Injectable, Self-Healing, Adhesive Multifunctional Hydrogel Promotes Bacteria-Infected Wound Healing

Bacterial infections have a serious impact on public health. It is urgent to develop antibacterial hydrogels with good biocompatibility to reduce the use of antibiotics. In this study, poly(lipoic acid-co-sodium lipoate)–phytic acid (P(LA-SL)-PA) hydrogels are prepared by a simple mixture of the natural small molecules lipoic acid (LA) and phytic acid (PA) in a mild and green reaction environment. The crosslinking network is constructed through the connection of covalent disulfide bonds as well as the hydrogen bonds, which endow the injectable and self-healing properties. The P(LA-SL)-PA hydrogels exhibit an adjustable compression modulus and adhesion. The in vitro agar plates assay indicates that the antibacterial rate of hydrogels against Escherichia coli and Staphylococcus aureus is close to 95%. In the rat-infected wound model, the P(LA-SL)-PA hydrogels adhere closely to the tissue and promote epithelialization and collagen deposition with a significant effect on wound healing. These results prove that the P(LA-SL)-PA hydrogels could act as effective wound dressings for promoting the healing of infected wounds.

Properties of road subbase materials manufactured with geopolymer solidified waste drilling mud

In this study, geopolymer was adopted as an eco-friendly binding material to solidify waste drilling mud to fabricate geopolymer solidified waste drilling mud (GSWDM) as a pavement material in the subbase. Using precursor dosage, Na2SiO3 solution dosage, and slag powder (SP) dosage as parameters of mix proportion, the optimal mix proportions of GSWDM were determined through compressive strength tests. Based on a series of tests of unconfined compressive strength, splitting tensile strength, elastic modulus, and compressive resilient modulus, the effects of the SP percentage in the precursor and curing age on the mechanical properties of GSWDM were analyzed. The results indicated that all the mechanical properties of GSWDM were improved with the increasing SP percentage in the precursor. The 28-day unconfined compressive strength, splitting tensile strength, elastic modulus, and compressive resilient modulus of GSWDM were improved by 80.8%, 56.3%, 65.3%, and 76.72%, respectively, when the SP percentage in the precursor increased from 60% to 100%. A nonlinear increase in the mechanical properties of GSWDM was observed as the curing age increased, with a significant increase in the curing age from 7 days to 14 days and a slight increase in the curing age from 14 days to 28 days. Moreover, the microstructure of GSWDM was denser as the curing age and the SP percentage in the precursor grew. The results of this study verified that GSWDM can be used as construction material for road subbase.

Real and In Silico Microgels Show Comparable Bulk Moduli Below and Above the Volume Phase Transition.

The compressibility of soft colloids influences their phase behavior and flow properties, especially in concentrated suspensions. Particle compressibility, which is proportional to the reciprocal of the bulk modulus K, is a key parameter for soft polymer-based particles that can be compressed in crowded environments. Here, microgels with different degrees of cross-linking, i.e.,softness, are investigated below and above their volume phase transition temperature (VPTT). By combining molecular dynamics simulations with small-angle neutron scattering with contrast variation, a change in the particle bulk moduli of two orders of magnitude is observed. The degree of cross-linking has a significant impact on the bulk modulus of the swollen microgel, while above the VPTT the values of K are almost independent of the cross-linking density. The excellent agreement between experimental results and simulations also highlight that the model microgels from computer simulationspossess both the internal architecture and the elastic properties of real polymeric networks. This paves the way to a systematic use of simulations to investigate the behavior of dense microgelsuspensions below and above their VPTT.

Investigation of the Influence of Alloy Atomic Doping on the Properties of Cu-Sn Alloys Based on First Principles

In order to design Cu-Sn alloys with excellent overall performance, the structural stability, mechanical properties, and electronic structure of X-doped Cu-Sn alloys were systematically calculated using first-principles calculations. The calculation results of the cohesive energy indicate that the Cu-Sn-X structures formed by X atoms (X = Ag, Ca, Cd, Mg, Ni, Zr) doping into Cu-Sn can stably exist. The Cu-Sn-Ni structure is the most stable, with a cohesive energy value of −3.84 eV. Doping of X atoms leads to a decrease in the bulk modulus, Possion’s ratio and B/G ratio. However, doping Ag and Ni atoms can improve the shear modulus, Young’s modulus, and strain energy of the dislocation. The doping of Ni has the highest enhancement on shear modulus, Young’s modulus, and strain energy of the dislocation, with respective values as follows: 63.085 GPa, 163.593 GPa, and 1.689 W/J·m−1. The analysis of electronic structure results shows that the covalent bond between Cu and X is the reason for the performance differences in Cu-Sn-X structures.

Thermal decomposition of oxygen‐containing Ta3N5${\rm {Ta}}_3{\rm {N}}_5$

AbstractTransition metal nitrides, especially tantalum nitrides, are pivotal for applications in extreme environments demanding excellent mechanical properties and thermodynamic stability. Among them, ‐TaN, a high‐pressure polymorph of tantalum nitride with its exceptional bulk modulus (362 GPa) and hardness (31.7 GPa) promises to have many technological uses. Another nitride, , has gained importance as a photocatalyst for water splitting using visible light. The Ta–N phase diagram indicates that the thermal decomposition of pure leads to the formation of ‐TaN. However, usually has some amount of oxygen as an impurity mainly due to its synthesis route. We found that the ‐TaN phase, which is usually observed at high pressures, is formed during the thermal decomposition of oxygen containing . The presence of ‐TaN is verified using several experimental techniques such as X‐ray diffraction, Raman spectra, high‐angle annular dark field scanning transmission electron microscopy (STEM‐HAADF), and electron energy loss spectroscopy (EELS). Elemental distribution analyzed through energy dispersion X‐ray spectroscopy (XEDS) in STEM reveals about 7 at.% of oxygen in ‐TaN. First‐principle calculations are performed to examine the thermodynamic stability of oxygen substituted ‐TaN and pure ‐TaN via formation enthalpies, elastic constants, and phonon dispersion calculations. The computational studies confirm that oxygen in ‐TaN enhances its thermodynamic stability. The calculated electron localization functions establish the bonding characteristics between Ta, N, and O, confirming the same.

Tunable Chemochromism and Elastic Properties in Intercalated MoO3: Au-, Cr-, Fe-, Ge-, Mn-, and Ni-MoO3.

Chemical tunability of the elastic constants of α-MoO3, a two-dimensional layered oxide, is demonstrated with mutability on the order of tens of GPa, simply by choice of a metal intercalant including Au, Cr, Fe, Ge, Mn, and Ni. Using Brillouin laser light scattering from confined acoustic phonons in nanometer-thick materials, the in-plane angular dispersion of the quantized acoustic phonon branches of 2D layered, intercalated MoO3 is measured and used to determine the bulk modulus (K), Young's moduli (E11, E22, and E33), each of the nine independent elastic tensor elements (cij), and the thickness. Intercalation of metals generally reduces the anisotropy in MoO3 except in Ge-MoO3, for which the in-plane longitudinal elastic anisotropy is unaffected. Chemochromism from transparent white (MoO3 and Fe-MoO3) to near black (Ni-MoO3) to brilliant dark blue (Ge-MoO3) is demonstrated and is associated with a reduction in electronic band gap with intercalation and an increase in absorption >600 nm for some intercalants (Cr-, Ge-, and Mn-MoO3).

Lightweight, mechanically robust and scalable cellulose-based foam enabled by organic-inorganic network and air drying

Lightweight and high-strength cellulose-based foams have gained increasing momentum due to their combination of sustainability and high performance. However, complex modification to cellulose fibers can sacrifice the environmental friendliness and further limit productional scalability. Here, we engineer lightweight yet strong cellulose-based foams made from mechanically treated microfibrillated cellulose (MFC), reinforced by organic-inorganic network, and scaled by surfactant foaming combined with air drying. Consisting of strong coordination and extensive secondary interaction within the organic-inorganic network, the resulting cellulose composite foams achieve both a high compressive modulus of 451.3 kPa and a yield strength of 25.1 kPa at a low density of 32.9 mg cm−3, which exceed other MFC-based foams based on surfactant foaming. In addition, the incorporation of the organic-inorganic network has no negative effect on the scalability, recyclability, or biodegradability of cellulose composites foam, making closed-loop material recycling possible. The life-cycle assessment reveals that replacing petroleum-based foams with our cellulose composite foams result in substantial reductions in carbon emissions. The structural design and manufacturing of our cellulose-based foam can stimulate market interest for cellulose foam and the development of the bioeconomy.