The aim of the present study was to examine effects of black liquor-montmorillonite (BL-Mnt) complexes on the mechanical and thermal properties of epichlorohydrin rubber. Considering the stability effect of lignin and the barrier property of clay minerals, a significant enhancement of thermo-oxidative aging properties of ECO/BL-Mnt composites was expected. Poly (epichlorohydrin-co-ethylene oxide) (ECO) composites filled with BL-Mnt complex were prepared by mechanical mixing on a two-roll mill. The ECO/BL-Mnt composites were characterized using X-ray diffraction (XRD), transmission electron microscopy (TEM), thermogravimetric analysis (TGA), and differential scanning calorimetry (DSC). Both XRD and TEM data showed that the filler particles were well dispersed throughout the ECO/BL-Mnt composites. The tensile strength, elongation at break, and 100% modulus of the rubber composite were 14.0 MPa, 457%, and 3.9 MPa, respectively, at a 50% loading of BL-Mnt. The retention of tensile strength was 99% after thermal oxidative aging in an air-circulating oven for 72 h at 100°C. Evidence indicated that ECO/BL-Mnt composites with good mechanical properties and thermo-oxidative aging properties were obtained.

The rheological characteristics of purified bentonite suspensions as a function of exchangeable cation $({\text{Ca}}^{2+},{\text{NH}}_4^{+},{\text{Li}}^{+})$$({\rm{C}}{{\rm{a}}^{2 + }},{\rm{NH}}_4^ + ,\;{\rm{L}}{{\rm{i}}^ + })$ are studied at three different clay concentrations (40 gL−1, 60 gL−1, 80 gL−1). A Herschel-Bulkley model is used to determine rheological parameters such as yield value, consistency and fluidification index. The flow curves are typical for shear thinning fluids but differ on two points; presence of yield stress and/or thixotropy. The Li suspensions are not yield stress fluid, and the thixotropy is weakly expressed only for the 80 gL−1 suspension. On the contrary, Ca-clay suspension flow curves always present yield stress and a large thixotropic area. The NH4-clay suspensions exhibit an intermediate behavior as there is no thixotropy, but a yield stress appears for the most concentrated suspension. These differences in macroscopic mechanical properties are discussed with reference to the suggested microscopic clay organization in suspension.

Mud shale is characterized by low strength and strong swelling, with rheological effects and deformation caused by drilling fluid and formation water. Establishing a rheological model to characterize the deformation characteristics is key to solving the problem of wellbore stability. The influence of moisture content on rock strength and creep mechanical properties were studied by means of water absorption, uniaxial compression, and creep tests. The tests showed that with the increase in moisture content, the elastic modulus and strength of hard brittle mud shale decreased. Further, under the same load, the instantaneous strain increased with increasing moisture content. Meanwhile, under various loading stresses, rock creep exhibited non-linear characteristics, which can be divided into three different creep stages: attenuated creep, stable creep, and accelerated creep. Starting with a non-linear viscous dashpot, and then introducing aging degradation and water-bearing weakening effects, based on the water-bearing creep characteristics of hard brittle shale as well as the modeling ideas of the classic component combination model, a new improved creep model based on the Nishihara model was established to describe the characteristics of the accelerated creep stage of hard brittle mud shale with various moisture contents. Subsequently, the Levenberg–Marquardt non-linear, least-squares method was adopted to invert the creep parameters. The results showed that the simulated creep curves achieved by employing the new creep model were consistent with the experimental results, thereby confirming the ability of the new non-linear creep model to provide a theoretical reference for the study of wellbore stability of hard brittle mud shale.

Enhancement of the physico-chemical properties of elastomers can be achieved by the addition of fillers, such as silica, but the search for less expensive alternative materials continues. The objective of this study was to investigate natural or organically modified clay minerals as such an alternative. Organo-clays modified by quaternary ammonium cations with three methyl groups and longest alkyl chains of different lengths were prepared by ion-exchange reaction of the commercial product JP A030 (Envigeo, Slovakia) based on Jelšový Potok bentonite with organic salts: tetramethylammonium (TMA) chloride, octyltrimethylammonium (OTMA) bromide, and octadecyltrimethylammonium (ODTMA) bromide. Physico-chemical characterizations of the organo-clays used as fillers in rubber nanocomposites and their mechanical properties were measured using Fourier transform infrared (IR) spectroscopy, which provided information on the chemical composition of the mineral and on the amount of organic moieties adsorbed. X-ray diffraction analysis (XRD) was used to monitor the arrangement of organic chains in galleries of montmorillonite and showed that the longest-chain alkylammonium ODTMA+ ions were intercalated between layers, adopting a pseudotrimolecular conformation, while OTMA+ and TMA+ were in monomolecular arrangement. Surface areas were measured by sorption of N2 and ethylene glycol monoethyl ether. Natural rubber-clay nanocomposites were prepared by melt intercalation, in some cases also with addition of silica, a conventional reinforcing filler. The microstructure of montmorillonite in these composites was characterized by XRD analysis. The effect of clay and organo-clays loading from 1 to 10 phr (parts by weight per hundred parts of rubber) on stress at break, strain at break, and Modulus 100 (M100) was investigated by tensile tests. Filler ODTMA-JP A030 appears to be the most effective among the organoclays; surprisingly similar values of composite elongation and strength were obtained with unmodified bentonite JP A030.

The negative effects of dye-contaminated wastewater on humans and the environment are well known, so the wastewater must be treated carefully before discharge into the environment. To overcome those impacts, the search for environmentally friendly and low-cost materials is essential, especially in developing countries The objective of the present study was to determine the feasibility of using bauxite from Malaysia as a new and efficient ceramic, hollow-fiber membrane for the degradation of reactive dyes in wastewater. A porous, hollow-fiber membrane was fabricated from bauxite (BHFM) using a phase-inversion technique, followed by sintering at various temperatures. The BHFM consisted of two types of voids, having either a finger-like or a sponge-like structure. As the sintering temperature was increased, the porosity of the BHFM decreased from 46.5 to 9.5%. The greatest mechanical strength of 308.1 MPa was achieved when the BHFM was loaded with 55 wt.% of bauxite and sintered at 1450°C. The remaining 45 wt.% consisted of solvent, polymer binder, and dispersant. The BHFM functioned well as a membrane for microfiltration and a support membrane for ultrafiltration. BHFM with loading of 45 wt.%, 50 wt.%, and 55 wt.% successfully eliminated 90%, 94%, and 98% of 10 ppm reactive dye (RB5) when sintered at the highest temperature.

The aim of the work was to study the effect of organo-montmorillonite (OMt) on the properties of hydrogenated nitrile rubber (HNBR)/OMt nanocomposites. The nanocomposites were prepared by a melt intercalation method. The structure of the composites was studied by transmission electron microscopy (TEM) and X-ray diffraction (XRD). The behavior of stress-strain, aging resistance, solvent resistance, and the dynamic mechanical properties of HNBR/OMt nanocomposites were investigated. The TEM and XRD results showed that the OMt layers were dispersed homogeneously in the HNBR matrix. The HNBR/OMt nanocomposites showed excellent mechanical properties which were attributed to the nanometer scale dispersion and strong interaction between the HNBR and OMt. The composites possessed excellent aging resistance and oil resistance, which improved with OMt content. Dynamic mechanical analysis showed that the glass-transition temperature, Tg, of the HNBR/OMt nanocomposites was increased and the nanocomposites had a good rolling resistance in comparison to pure HNBR. The composites displayed better dynamic mechanical properties.

To investigate the influence of clay mineral microstructures on mechanical properties across varying hydration levels, this study employed molecular dynamics simulations to conduct uniaxial tensile strength tests in three orthogonal directions (x, y, z) using illite, montmorillonite and kaolinite. The moisture content was varied from 0% to 10% in 1% increments and from 0% to 50% in 10% increments. The observations highlight the role of water molecules in disrupting the inherent microscopic atomic structure of clay minerals, leading to diminished stability and a decline in tensile strength. As moisture content increased, there was a pronounced increase in the layer spacing of all three clay minerals, indicative of their hydration expansion behaviour. Concurrently, discernible reductions in both the tensile strength and Young's modulus of the clay minerals were observed.

Uniaxial and isothermal compression tests of kaolinite were carried out using molecular dynamics simulations. Five different temperatures (300, 400, 500, 600 and 700 K) and pressures ranging from 0.0001 to 50 GPa were selected to study the temperature and pressure effects on the mechanical properties of kaolinite. As kaolinite may undergo a phase transition at ~1572 K, a highest temperature of 700 K was chosen to avoid such structural change. The Young's modulus, strength and elastic constants of kaolinite under various temperatures were calculated, and the relative change of the elastic constant C33 with temperature was found to be almost 12 times greater than the relative change of the interlayer constant C11. The microstructures under various compressive strains were tracked and they exhibited various failure modes in three directions. The temperature and pressure effects on the mechanical properties of three crystal directions were analysed. The results showed that the Young's modulus of the z-direction is the most affected by temperature; however, the influence of temperature on the strengths of the three crystal directions was the same. In addition, the structure of the z-direction was the most sensitive to temperature under the same hydrostatic pressure due to the weak interactions between layers.

Plants acclimate to various types of mechanical stresses through thigmomorphogenesis and alterations in their mechanical properties. Although resemblance between wind- and touch-induced responses provides the foundation for studies where wind influence was mimicked by mechanical perturbations, factorial experiments revealed that it is not always straightforward to extrapolate results induced by one type of perturbation to the other. To investigate whether wind-induced changes in morphological and biomechanical traits can be reproduced, we subjected Arabidopsis thaliana to two vectorial brushing treatments. Both treatments significantly affected the length, mechanical properties and anatomical tissue composition of the primary inflorescence stem. While some of the morphological changes were found to be in line with those induced by wind, changes in the mechanical properties exhibited opposite trends irrespective of the brushing direction. Overall, a careful design of the brushing treatment gives the possibility to obtain a closer match to wind-induced changes, including a positive tropic response.

With the aim of optimizing the traditional construction process of a fiber-reinforced lattice structure, the present study modified a previously proposed technique called “truss stacking and node gluing.” To explicitly investigate the structural compressive properties (compressive strength and compressive modulus under the flat pressure), the geometrical parameters, material properties, and topological configuration were examined in detail. Additionally, the present study conducted the relevant theoretical analyses to predict the possible destruction modes and compressive properties. All the samples were tested with a universal testing machine at a rate of 2 mm/min using the ASTM-C365 standard. The results showed that compressive properties are positively related to the relative density and negatively related to the aspect ratio. It was also found that the compressive performance for different materials was in the following order (from good to bad): cotton-fiber reinforced epoxy composite (CREC), jute-fiber reinforced epoxy composite (JREC), and nylon-fiber reinforced epoxy composite (NREC). Furthermore, the mixed topological structure performed as well as the square structure, and they both overmatched the diamond structure. Lastly, the accuracy of the theoretical analysis was evaluated by comparing the theoretical values and the experimental values.

Al0.1CoCrFeNi high-entropy alloy (HEA) was synthesized successfully from elemental powders by mechanical alloying (MA) and subsequent consolidation by spark plasma sintering (SPS). The alloying behavior, microstructure, and mechanical properties of the HEA were assessed using X-ray diffraction, electron microscope, hardness, and compression tests. MA of the elemental powders for 8 h has resulted in a two-phased microstructure: α-fcc and β-bcc phases. On the other hand, the consolidated bulk Al0.1CoCrFeNi-HEA sample reveals the presence of α-fcc and Cr23C6 phases. The metastable β-bcc transforms into a stable α-fcc during the SPS process due to the supply of thermal energy. The hardness of the consolidated bulk HEA samples is found to be 370 ± 50 HV0.5, and the yield and ultimate compressive strengths are found to be 1420 and 1600 MPa, respectively. Such high strength in the Al0.1CoCrFeNi HEA is attributed to the grain refinement strengthening.

The effects of the Mg/Si ratio and aging treatment on the strength and electrical conductivity of Al–Mg–Si 6201 conductor alloys were investigated. Four experimental alloys with different Mg/Si ratios of 2, 1.5, 1, and 0.86 and with a constant Mg level of 0.65 wt% were prepared. It was revealed that excessive Si (a low Mg/Si ratio) increased the peak strength, while the corresponding electrical conductivity decreased. To fulfill the minimum required electrical conductivity (52.5% IACS), the alloys with low Mg/Si ratios required a longer aging time after peak aging to improve electrical conductivity. The alloy with an Mg/Si ratio of ~1 was the best candidate, exhibiting the highest strength up to 54% IACS. On the high end of electrical conductivity (54–56% IACS), the alloy with an Mg/Si ratio of ~1.5 provides a better compromise between strength and electrical conductivity. Furthermore, the strengthening mechanisms and the factors influencing electrical conductivity were discussed for further optimization.

The CoCrNiMox (x = 0, 0.1, and 0.2 in molar ratio) medium entropy alloys (MEAs) were fabricated by vacuum arc melting, followed by cold rolling and annealing treatments. The X-ray diffraction (XRD), electron back-scattered diffraction (EBSD), and transmission electron microscopy (TEM) were employed to characterize the microstructures. It has been shown that the CoCrNi MEA has a single FCC phase and the Mo-containing MEAs contain (Cr, Mo)-rich σ precipitates. In addition, the Mo addition caused significant grain refinement, due to the fact that the presence of σ phase exerts a strong pinning effect on the grain boundary migration. The hardness testing results indicate an increment in Vickers hardness from 187.5 ± 4.5 Hv of CoCrNi alloy to 309.5 ± 10.3 Hv of CoCrNiMo0.2 alloy. The yield strength and ultimate tensile strength also increase from 339 ± 2 to 644 ± 5 MPa and from 810 ± 5 to 1071 ± 17 MPa, respectively, but the elongation drops from 88.4 ± 4.0% to 29.5 ± 7.6%. The grain refinement and the precipitation of σ phase make synergistic contribution to the reinforcement of Mo-containing CoCrNi-based MEAs. The details and explanations in this study may guide the future design and research of the CoCrNi-based quaternary alloys with enhanced properties.

In the present paper, the authors investigated the microstructures and mechanical properties of dual-phase Co–Ti–V-based superalloys with different additions of Ru. The results showed that with the increase of Ru contents, the size of γ′ precipitates of the alloy gradually raised, the volume fraction of γ′ phase slightly, and the lattice misfit between γ/γ′ phases increased. Ru was enriched in the γ′ phase, and the elemental partition coefficients (KX = Cγ′/Cγ) of Ti and V increased with the increment of Ru. The Ru contents have no remarkable influence on the solvus temperatures of γ′ in the Co–Ti–V alloys. The yield strength at 1000 °C of the Co–10Ti–11V–0.5Ru alloy was the highest, while the yield strength of the 1Ru alloy was the smallest. Transmission electron microscopy and scanning electron microscopy observations showed that the γ′ shape in the compressed specimen containing 0.5Ru remain integrated, while the γ′ in other alloys were cut into several parts.

In the present work, the effect of annealing temperature on the microstructure, mechanical and tribological properties of NiCr–WC–Co coatings produced by the high-velocity oxy-fuel (HVOF) technique has been investigated. X-ray diffraction and scanning electron microscopy revealed the dissolution of WC into the NiCr matrix to form W2C and Cr3C2 with the annealing process. This dissolution became complete at 800 °C. The mechanical properties of the coatings were investigated using nano-indentation and Vickers fracture toughness measurements. These measurements suggested that the hardness, Young's modulus, and fracture toughness values increased because of the newly formed carbide phases as a result of the dissolution of the WC particles. The overall properties of the coatings were found to be optimum for annealing temperatures of 800 °C. The wear mechanism appears to be abrasive in the as-sprayed coating, and it becomes a combination of an abrasive and oxidative wear with increasing the annealing temperature.

The influence of excess Al2O3 on 3:2 mullite produced from α-Al2O3 and pyrophyllite powder was examined. A mixture consisting of 28 wt.% dehydroxylated pyrophyllite and 72 wt.% α-Al2O3 was milled in an attrition mill. The milled powders were sintered by spark plasma sintering (SPS) at 1600°C for 10, 20 and 30 min. Subsequently, the samples were heated at 1350°C for 2 h to determine the influence of the excess Al2O3 on the microstructure. No glassy phase was detected in the sample containing 72 wt.% Al2O3 and sintered at 1600°C for 20 min. The sample with 72 wt.% Al2O3 had greater hardness and fracture toughness compared to 3:2 mullite. The greatest hardness and fracture toughness of 12.43 GPa and 2.71 MPa m–0.5, respectively, were obtained in the sample containing 72 wt.% Al2O3 sintered at 1600°C for 20 min.

TiAl alloys are potential structural high-temperature structural materials at a service temperature of ~900 °C, while poor ductility at room temperature and high creep rate at the elevated temperature limits the applications. To improve the room-temperature and high-temperature mechanical properties of Ti–44Al–5Nb–3Cr–1.5Zr, Mo and B were introduced into this system and Ti–44Al–5Nb–3Cr–1.5Zr–xMo–yB alloys were proposed. And then, we, respectively, studied the microstructures and mechanical properties of Ti–44Al–5Nb–3Cr–1.5Zr–xMo–0B and Ti–44Al–5Nb–3Cr–1.5Zr–1Mo–yB to elucidate the role for the addition of Mo and B. It is found that Mo can increase the fraction of B2 phase in the alloys and the microstructures of the alloys are greatly refined by the addition of B. The compression test results indicate that Mo has a positive influence on the high-temperature compressive properties of TiAl-based alloys, whereas B addition can improve their room-temperature compressive properties of Ti–44Al–5Nb–3Cr–1.5Zr–1Mo–yB alloys; the morphology of borides in each sample should be the structural origin for these phenomena.

In this investigation, the superalloy IN718 has been prepared by additive manufacturing (AM) following a selective laser melting technique, and the post-AM heat treatments have been optimized. The microstructure of additively manufactured (AM) IN718 is characterized by the presence of dendritic and cellular features with large spatial heterogeneity along and across the build plane. Along the build direction, the 〈100〉 fiber texture dominates. Heat treatment involving two-step solution treatment, and subsequently, two-step aging treatment was specifically designed to facilitate the precipitation of δ phase at the grain boundaries to make the material resistant to grain boundary sliding (GBS). The AM IN718 showed dynamic strain aging (DSA) at three different temperatures, while the critical strain for the onset of serration was extended to a higher value after the heat treatment.

In this paper, CNTs reinforced foam aluminum matrix composites with small pore diameter were prepared by powder metallurgy method. When the mass fraction of CNTs was 0.75%, the tensile strength, flexural strength and compressive yield strength of the materials were 3.4 times, 2.4 times and 2.4 times of pure foam aluminum, respectively, reaching the maximum value, which obviously improved the mechanical properties of aluminum foam. The tensile property model of foam aluminum matrix composites was built to predict the properties of the composites, and the effects of defects and reinforcement on the mechanical properties of the composites were compared. The results show that the tensile fitting is consistent with the measured results when the mass fraction of CNTs is less than 0.75%, but the weakening effect of defects on the strength of aluminum foam is much greater than the enhancement of CNTs. With the increase of CNTs mass fraction, the damping loss factor of foam aluminum composites increases, dislocation damping and grain boundary damping play a role in advance, and the damping peak moves to the low temperature region.