Interfacial Behavior Research Articles

Moiré superlattice effects on interfacial mechanical behavior: A concise review

AbstractThe moiré superlattice, arising from the interface of mismatched single crystals, intricately regulates the physical and mechanical properties of materials, giving rise to phenomena such as superconductivity and superlubricity. This study delves into the profound impact of moiré superlattices on the interfacial mechanical behavior of van der Waals (vdW) layered materials, with a particular focus on tribological properties. A comprehensive review of continuum modeling approaches for vdW layered materials is presented, accentuating the incorporation of moiré superlattice effects in theoretical models to unravel their distinctive interfacial frictional behavior and thermodynamic properties. The exploration of moiré superlattices has significantly advanced our fundamental understanding of interface phenomena in vdW layered materials. This progress provides crucial theoretical insights that can inform the design of multifunctional devices based on the unique properties of twisted layered materials.

Understanding the foam stability mechanisms of complex formed by soy protein isolate and different charged polysaccharides: Air/water interfacial behavior and rheological characteristics

This study evaluated the foaming properties, the dynamic adsorption behavior at the air/water (A/W) interface and the foam rheological characteristics of complexes formed by soy protein isolate (SPI) and different charged polysaccharides, including chitosan (CS), guar gum (GUG) and gellan gum (GEG). The results showed that the SPI/CS10 had the highest initial foam volume (26.67 mL), which were 3.89 %, 100.08 % and 70.19 % higher than that of single SPI, SPI/GUG and SPI/GEG complexes, respectively. Moreover, three charged polysaccharides could all significantly improve the foam stability of complexes. Among them, foams stabilized by SPI/GEG10 were the most stable that the foam volume slightly changed (approximately 1 mL) and no drainage occurred throughout the whole recording process. The interfacial behavior analysis showed that SPI/CS10 had higher diffusion (Kdiff) and rearrangement rate (KR) but lower penetration rate (KP) at the A/W interface compared with single SPI, while SPI/GUG10 and all SPI/GEG complexes showed higher KR and KP but lower Kdiff. In addition, SPI/CS10 was beneficial to concurrently enhance the elastic strength and solid-like behavior of foam system, while all SPI/GEG complexes could improve the elastic strength of foam system but was not conducive to the solid-like behavior.

A multiscale experimental study of CFRP-UHPFRC interfacial bond behaviour: Failure mechanisms and a fibre volume dependent bond-slip law

Carbon fiber reinforced polymer (CFRP) materials are being increasingly used with ultra high performance fiber reinforced concrete (UHPFRC) to construct composite structural members making use of their unique properties. As the interfacial bond behaviour between CFRP and UHPFRC plays a key role in the design of such members, it was investigated in detail by multiscale experiments of single shear pull-off tests of 26 CFRP-UHPFRC bonded joints with different bond lengths and widths of CFRP laminates and 0.5–4% volume fraction (Vsf) of straight high-strength steel fibers (length = 13 mm, diameter = 0.2 mm). 12 CFRP-normal strength concrete (NSC) bonded joints were also tested for comparison. The surface strain evolution and the interfacial debonding process were captured and analysed by the digital image correlation (DIC). The complex microscale failure mechanisms, such as the mortar cracking, the CFRP-UHPFRC interfacial debonding, and the steel fibers’ slipping and pulling out of the mortar, were visualised and analysed by the 3D micro X-ray Computed Tomography (μXCT) scanning. It was found that the debonded layer of mortar under the laminates was much thinner than that in the CFRP-NSC bonded joints, due to the lack of coarse aggregates in UHPFRC. The peak pulling forces for the specimens with Vsf = 0.5%, 1%, 2%, and 4% were 9%, 21%, 28%, and 29% higher than those without steel fibers, respectively. An empirical bond strength model and an interfacial bond-slip model were proposed based on the test results, accounting for Vsf, the material properties, and the laminate to UHPFRC width ratio. Finally, the proposed bond-slip model was applied in finite element modelling to simulate the flexural behaviour of an FRP-UHPFRC composite deck in the literature, with the interfacial debonding failure and the ultimate loads successfully predicted.

Structural design, interfacial behavior and mechanical properties of bimetallic nacre-like structures by laser powder-bed fusion

The nacre-like (NL) structure exhibits unique performance in preventing the catastrophic crack growth and improving the strengthening/toughening of the overall structure. In this study, the In718/316LSS bimetallic NL structures were first fabricated by a powder laying-absorption multiple-material additive manufacturing technology based on laser powder-bed fusion, and the stress release mechanism was revealed. The NL structures with optimal geometric parameters was obtained by calculation and simulation: the hard-phase inclination angle of 15 °, the hard-phase volume fraction of 70%, and the lamellar length-width ratio of 2. Due to the remelting effect, the same-layer bimetallic interfaces in NL structures showed strong metallurgical bonding with significantly grain refinement. The interlocking NL structure exhibited superior mechanical properties of 751.82 MPa in tensile strength and 25.14% in elongation, compared with the base alloys and the non-interlocking NL structure. Moreover, abnormal variation of work hardening rate in NL structures attributed to the stress concentration and release behavior, caused by the multi-cracks initiation and cracks deflection during deformation of the interlocking structure. By the stress concentration-release effect, the NL structure not only achieved the strengthening and toughening, but also improved the crack tolerance to avoid the sudden fracture failure.

Formation of interfacial molecular film and metal‐trapping function of azacalixarene‐containing copolymers having spherulite‐forming ability

AbstractThe interfacial molecular film behavior of a newly synthesized copolymer having spherulite‐forming ability and consisting of an azacalixarene moiety and a polyethylene glycol linker was investigated. Furthermore, the ability of the azacalixarene ring in the copolymer Langmuir monolayer to trap metals from the subphase was examined. The copolymer formed a monolayer at the air/water interface with high‐density packing. In addition, the corresponding copolymer formed a stable interfacial monolayer whose behavior did not change significantly as the temperature of the subphase changed. The monolayer morphology exhibited a dot‐like crystalline domain. When the subphase contained cadmium ions, the cyclic moiety showed the ability to trap the metal cations. In this case, the distortion angle of the cup‐shaped conformation of the cyclic moiety in the organized molecular film expanded after metal trapping.Highlights LB film of a copolymer containing azacalixarene and PEG units was prepared. The copolymer formed a dense packing in the LB film. Copolymer film formed a surface morphology containing crystalline grains. The copolymer trapped Cd ions in the azacalixarene ring from the subphase. Due to trapping of Cd ions, the distortion angle of the ring widened by 7°.

Adsorption Layer Properties and Foam Behavior of Aqueous Solutions of Whey Protein Isolate (WPI) Modified by Vacuum Cold Plasma (VCP)

For years, cold plasma processing has been used as a non-thermal technology in industries such as food. As interfacial properties of protein play a remarkable role in many processes, this study investigates the effect of cold plasma on the foaming and interfacial behavior of WPI. The objective of this study is to evaluate the effect of different gases (air, 1:1 argon–air mixture, and sulfur hexafluoride (SF6)) used in low-pressure cold plasma (VCP) treatments of whey protein isolate (WPI) on the surface and foaming behavior of aqueous WPI solutions. Dynamic surface dilational elasticity, surface tension isotherms, surface layer thickness, and the foamability and foam stability were investigated in this study. VCP treatment did not significantly affect the adsorption layer thickness. However, an increase in induction time, surface pressure equilibrium value, and aggregated size is observed after SF6VCP treatment, which can be attributed to the reaction of WPI with the reactive SF6 species of the cold plasma. The surface dilational elastic modulus increased after VCP treatment, which can be related to the increased mechanical strength of the protein layer via sulfonation and aggregate formation. VCP treatment of WPI increases the foam stability, while the average diameter of foam bubbles and liquid drainage in the foam depends on the gas used for the cold plasma.

Ultrafast piezocapacitive soft pressure sensors with over 10 kHz bandwidth via bonded microstructured interfaces

Flexible pressure sensors can convert mechanical stimuli to electrical signals to interact with the surroundings, mimicking the functionality of the human skins. Piezocapacitive pressure sensors, a class of most widely used devices for artificial skins, however, often suffer from slow response-relaxation speed (tens of milliseconds) and thus fail to detect dynamic stimuli or high-frequency vibrations. Here, we show that the contact-separation behavior of the electrode-dielectric interface is an energy dissipation process that substantially determines the response-relaxation time of the sensors. We thus reduce the response and relaxation time to ~0.04 ms using a bonded microstructured interface that effectively diminishes interfacial friction and energy dissipation. The high response-relaxation speed allows the sensor to detect vibrations over 10 kHz, which enables not only dynamic force detection, but also acoustic applications. This sensor also shows negligible hysteresis to precisely track dynamic stimuli. Our work opens a path that can substantially promote the response-relaxation speed of piezocapacitive pressure sensors into submillisecond range and extend their applications in acoustic range.

Revolutionizing Dental Implant Research: A Systematic Review on Three-Dimensional In Vitro Models.

Dental implants have been clinically used for almost five decades with high success rates. In vitro research models used in implant dentistry are limited to two-dimensional experiments, which are reproducible and well adapted to evaluate a single parameter but do not reproduce the complexity of clinical settings. On the contrary, the in vivo research models using animals offer similar histological and anatomical features to humans, and tissue healing can be close to a clinical situation, but those models are usually accompanied with ethical concerns, and their outcomes could not be extrapolated to humans because of interspecies variabilities. This makes the development of novel in vitro models that recapitulate physiological events occurring during dental implant placement of particular interest for current research in dentistry. Also, such models could be challenged by setting a pathological environment (peri-implantitis) to better understand the disease and eventually serve as a platform to evaluate novel treatment modalities. The aim of this systematic literature review was to cover all the in vitro three-dimensional (3D) complex models available for research in implant dentistry. To accomplish this, a comprehensive search of the literature present on Scopus and PubMed databases was done using specific keywords, as well as inclusion/exclusion criteria. Out of 1334 articles found, we have finally included 27 articles in this review with publication dates between 2001 and 2022. In those articles, the 3D models were designed to study tissue-implant interface behavior in bone or gingival tissue. The articles focused on simulating implant integration, evaluating the effect of different conditions on implant integration, or developing an infection model for the implant integration process. The methods used involved implant material and cells organized in a specific 3D structure. The 3D models developed were able to simulate the process of dental implant osseo- and soft tissue integration and lead to results comparable with conventional in vitro and in vivo models. A relatively limited number of articles were obtained, which indicates that this is an emerging field, highly dependent on progresses made in biotechnologies and tissue engineering, and that further investigation is needed to enhance these 3D in vitro models.

The effect of shear rate and overconsolidation ratios on undrained clay–suction caisson interface behaviors

The interface resistance during installation is crucial for the stability and safety of suction caisson in offshore geotechnical engineering, which is strongly affected by the penetration rate and soil–structure interface mechanical properties. This research conducts a series of clay–structure interface shear tests using modified direct simple shear device to fully study the mechanical behavior of clay–suction caisson interface. The effect of shear rate, over consolidation ratios (OCRs), interface boundary conditions, stress levels, and interface roughness were considered. Results show that as the OCR increases, the strength of both the clay and interface increase but show distinct patterns under constant volume (CV) and constant normal load (CNL) boundary condition. It was found that the interface strength is positively related to interface roughness and shear rate impact both the clay and corresponding interface strength. Under CNL conditions, the strength of normally consolidated (NC) clay decreases with rising shear rate, while the over consolidated (OC) clay demonstrate a opposite trend. In contrast, the effect of shear rate on interface behavior gets complicated owing to the combination of roughness, stress levels, and OCRs. Under CV conditions, the shear strength of clay and interface exhibits a logarithmic growth relationship with shear rates. The result of this work can provide a basis for interface resistance evaluation for suction caisson installation in clay.

Vicinal (111) surfaces at Si solid-liquid interface during unidirectional solidification

The solid-liquid interfaces of silicon grains have been observed by an in-situ system. Two silicon seeds having different crystallographic orientations (as ⟨100⟩, ⟨110⟩, and ⟨111⟩) along the growth direction were placed side by side in a silica crucible for the direct comparison of interface behavior during the melt-growth process. Experimental evidence proved the existence of flat {111} surfaces at different grain orientations during crystallization. The difference in the interface positions of the two grains was used to calculate the undercooling of the {111} surfaces. The growth rate-undercooling relationship was linear in all experiments, showing that the observed flat surfaces were planes vicinal to {111} facets, growing through a step flow mode. The terrace length was constant but different from one experiment to another. Therefore, this work indicates that it is crucial to consider the vicinal surface kinetics in the analysis of Si facet planes and grooves during the melt-growth process.

A new peridynamic interface model for fracture analysis of imperfect interface

In this study, a new peridynamic interface model is proposed for the imperfect interface fracture analysis. The peridynamic interface bonds are defined for the imperfect interface modeling, and formations of bond normal and tangential interface forces are given. An extended critical bond energy density-based criterion is proposed for interface bonds failure analysis, and mixed-mode fracture mode is considered. Three specimens bonded with the imperfect interface are analyzed to verify the peridynamic interface model. The bonded deformation and fracture behaviors of imperfect interface are predicted with the proposed model, and compared to those from the theoretical and FEM results. The comparisons demonstrate that the proposed peridynamic interface model can well capture the deformation and fracture behaviors of the imperfect interface.

Understanding the Interfacial and Self-Assembly Behavior of Multiblock Copolymers for Developing Compatibilizers toward Mechanical Recycling of Polymer Blends

Understanding the Interfacial and Self-Assembly Behavior of Multiblock Copolymers for Developing Compatibilizers toward Mechanical Recycling of Polymer Blends

Fabrication of GNPs sprayed carbon fiber and its effects on the interfacial and mechanical behavior of reinforced epoxy multiscale laminated composite

AbstractThe current research compares the effects of modifying carbon fiber [via spraying graphene nanoplates (GNPs)] and/or GNPs reinforcement on the mechanical and interfacial behavior of carbon fiber epoxy composites. Using a spraying method, the epoxy matrix was reinforced, and carbon fiber was modified with 0.2 and 1 wt% of GNPs, respectively. Tensile, interlaminar, and dynamic mechanical analyses (DMA) tests were conducted on the composite to assess the role of GNPs in enhancing mechanical, interfacial, and thermomechanical properties. The obtained results indicate that the spraying technique effectively enhanced the ultimate tensile strength (UTS) and interlaminar fracture toughness (ILFT) of the composite. The UTS improved by 31%, while the ILFT significantly improved by 38%. Additionally, assessing the modulus gradient through the interface shows improved interfacial interaction between modified carbon fiber and reinforced epoxy. Scanning electron microscopy examination of the fractured surfaces indicated that the existence of nanofillers with high surface area contributed to significant improvements in adhesion between the modified fiber and reinforced epoxy matrix, leading to enhanced interfacial, mechanical, and thermomechanical properties of CFRPs for structural applications.Highlights Incorporation of surface modified carbon fibers and GNPs reinforcement in the epoxy matrix to enhance the interfacial interaction. Evaluation of the effects of GNP nanofiller on interfacial and mechanical performance of the composite. Fracture surfaces in ILSS, tensile, and mode I test were analyzed using FESEM. Utilization of nanoscale modulus mapping for the fiber‐matrix interface assessment.

Exploring the effect of relaxation time, natural surfactant, and potential determining ions (Ca2+, Mg2+, and SO42−) on the dynamic interfacial tension behavior of model oil-brine systems

This study examined how the concentration of asphaltene and divalent ions in various salinities affects the interfacial tension (IFT) between a model oil/brine using the pendant drop method. The oleic phase consisted of a mixture of toluene and n-heptane (heptol), to which asphaltene was added to investigate how asphaltene molecules affect the surface properties. The base fluid was prepared with a salinity of 40,000 ppm, and two additional solutions with concentrations of 4000 ppm (low salinity) and 80,000 ppm (high salinity) were created. The results revealed that increasing the concentration of asphaltene within certain salinity ranges led to a decrease in IFT. The lowest IFT was observed at the 40,000 ppm salinity level, indicating that at this optimal salinity, the maximum asphaltene concentration migrated to the heptol/brine interface, reducing the IFT from 23 mN/m to 16 mN/m. Additionally, a 0.5% wt of asphaltene demonstrated a significant concentration of micellization of natural surfactants, suggesting that the interface was nearly saturated with asphaltene. Consequently, concentrations higher than this value did not significantly alter the IFT. In the final part of the study, the impact of divalent ions was investigated, revealing that as the concentration of Ca2+ ions increased up to fourfold, the IFT decreased to 15 mN/m, about 10% less than the base case. This value represented the lowest IFT compared to Mg2+ and SO42−. Moreover, modeling the results indicated that the relaxation time decreased with increasing salinity, suggesting that higher salinity accelerated the process of asphaltene absorption at the interface.

Macro and mesoscopic shear behavior of interface between sand and concrete with different JRC under cyclic load

Macro and mesoscopic shear behavior of interface between sand and concrete with different JRC under cyclic load

Testing and identification method for the interfacial heat transfer coefficient between CFRTP and tools under fast hot-stamping conditions

Carbon fiber reinforced thermoplastic composites (CFRTP) are increasingly applied in automobile structures. Hot-stamping is a fast forming process for complex components of CFRTP. During hot-stamping process, the variations of temperature field occur in entire forming process, which ultimately have an impact on the forming quality and dimensional precision of the part. The interfacial heat transfer behaviour between CFRTP and tools directly determines the temperature distribution in the part. However, the existing heat transfer testing and identification methods are designed for sheet metal, which may not be applicable for CFRTP due to the differences in material properties and forming processes. Therefore, in this work, a new test device was developed to reproduce the interfacial heat transfer behaviour of CFRTP under various hot-stamping conditions, and an inverse identification method of the interfacial heat transfer coefficient (IHTC) between CFRTP and tools was proposed. The influences of contact conditions on the IHTC were investigated, including the interfacial contact pressure, interfacial clearance, heating temperature of tools and sheets. The results showed that the IHTC demonstrated a positive correlation with the contact pressure. However, the IHTC would significantly decrease with the existence of a clearance at the interface. Within the entire heat transfer process, it was also found that an increase in tool temperature resulted in a decrease in the IHTC, while initial sheet temperature didn't exert a significant influence. Furthermore, the reliability of proposed testing and identification methods had been verified by the hot-stamping for U-shaped CFRTP parts. The temperature error between the simulation and experiment was less than 5 %.

Closely Packed Core-Shell Micelle Structures of Double Hydrophilic Miktoarm Star Copolymers at the Air-Water Interface.

The aggregation behavior of amphiphilic block copolymers at the air-water interface has been extensively studied, but less attention was given to that of star copolymers. In this work, we studied the interfacial aggregation behavior of two double hydrophilic pH- and temperature-responsive miktoarm star copolymers of poly[di(ethylene glycol) methyl ether methacrylate]-poly[2-(dimethylamino)ethyl methacrylate] (PDEGMA3-PDMAEMA3 and PDEGMA4-PDMAEMA7, the subscripts denote arm numbers) with different molecular weights. The effects of subphase pH and temperature on the monolayer isotherms and hysteresis curves of the two star copolymers and the morphologies of their Langmuir-Blodgett (LB) films were studied by the Langmuir film balance technique and atomic force microscopy, respectively. At the air-water interface, the two star copolymers tend to form closely packed micelles. These micelles exhibit a core-shell structure, where the small hydrophobic core consists of cross-linker of ethylene glycol dimethacrylate (EGDMA) and the carbon backbones of PDEGMA and PDMAEMA arms and the short hydrophilic shell is composed of di(ethylene glycol) and tertiary amine side groups. With increasing subphase pH, the surface pressure versus molecular area isotherms shift toward larger mean molecular areas as a result of the enhanced interface adsorption of nonprotonated tertiary amine groups. The isotherm shift of PDEGMA3-PDMAEMA3 monolayers is primarily attributed to high density of tertiary amine groups in the shells, while that of PDEGMA4-PDMAEMA7 is mainly attributed to high density of di(ethylene glycol) groups in the shells. The hysteresis degrees in the monolayers of the two copolymers under alkaline and neutral conditions are greater than those under acidic conditions due to the decreased protonation degree of the tertiary amine groups. At 10 °C, the mobility of the shells is poor and the isotherms are located on the right. Above the lower critical solution temperature, di(ethylene glycol) groups contract, which causes a slight shift of the isotherms toward smaller mean molecular areas.

Effect of Soil-Structure Interaction on the Response of Machine Foundation Subjected to Seismic Loading: A Review Study

This review provides a detailed look at the current knowledge and approaches related to Dynamic Soil-Structure Interaction (DSSI) in machine foundation design, focusing on its substantial impact on seismic response and structural stability. The significance of this interaction in structural design, especially in areas prone to seismic activity, is pivotal. The paper begins by exploring various modeling methods, like the Finite Element Method (FEM), highlighting their importance in understanding the intricate aspects of DSSI, such as energy loss and interface behavior. It is evident from the studies that FEM is particularly effective in analyzing settlement under reciprocating loads. Soil-structure interaction (SSI) is a complex phenomenon that can positively and negatively affect the seismic performance of machine foundations. Several factors, including embedment depth, soil stiffness, and foundation properties, govern the influence of SSI. This review discusses the dual nature of SSI and highlights the importance of considering the interaction between soil properties, foundation design, seismic loads, and interaction effects. In addition, it identifies the limitations of the current research and advocates for more accurate and inclusive models and extensive empirical studies to address real-world complexities and uncertainties. In conclusion, this review offers crucial insights and foundational knowledge for future innovative design solutions and advanced research methodologies and significantly contributes to developing resilient and reliable structural designs in seismic-prone regions. The emphasis is on the need for more nuanced and comprehensive studies to further the understanding and application of DSSI in machine foundation design.  

Quantum Dots on a String: In Situ Observation of Branching and Reinforcement Mechanism of Electrospun Fibers.

Immobilization of quantum dots (QDs) on fiber surfaces has emerged as a robust approach for preserving their functional characteristics while mitigating aggregation and instability issues. Despite the advancement, understanding the impacts of QDs on jet-fiber evolution during electrospinning, QDs-fiber interface, and composites functional behavior remains a knowledge gap. The study adopts a high-speed imaging methodology to capture the immobilization effects on the QDs-fiber matrix. In situ observations reveal irregular triangular branches within the QDs-fiber matrix, exhibiting distinctive rotations within a rapid timeframe of 0.00667ms. The influence of FeQDs on Taylor cone dynamics and subsequent fiber branching velocities is elucidated. Synthesis phenomena are correlated with QD-fiber's morphology, crystallinity, and functional properties. PAN-FeQDs composite fibers substantially reduced (50-70%) nano-fibrillar length and width while their diameter expanded by 17%. A 30% enhancement in elastic modulus and reduction in adhesion force for PAN-FeQDs fibers is observed. These changes are attributed to chemical and physical intertwining between the FeQDs and the polymer matrix, bolstered by the shifts in the position of C≡N and C═C bonds. This study provides valuable insights into the quantum dot-fiber composites by comprehensively integrating and bridging jet-fiber transformation, fiber structure, nanomechanics, and surface chemistry.

Stabilizing Interfacial Behaviors of Ni‐rich Cathodes by Upcycling of Oyster Shells Waste

AbstractLayered lithium oxides (LNCM), with over 60% Ni, are promising cathode materials for electric vehicles due to their high capacity. however, reliable cycling retention cannot easily achieved owing to the instability of the interface. Here, recycled oyster shell (OS) is employed as an efficient precursor for the surface modification of LNCM cathodes; subsequently, Ca‐based artificial cathode–electrolyte interphases (CEI) are obtained at the LNCM interfaces through a simple calcination process. When the pulverized OS is calcined with LNCM cathode materials at elevated temperatures, CaCO3 is converted to CaO via thermal decomposition at the LNCM interface, which effectively protects the unstable interface. Microscopic analyses indicate the nanodomain island‐type CEI layers embedded after OS calcination. The OS‐coated LNCM cathode materials increase the cycling retention after 100 cycles (93.8% vs. 62.7%) and decrease the internal cell pressure by preventing electrolyte decomposition. Incorporating Ca into the LNCM cathode materials also inhibits microcrack formation because of the improvement in particle hardness and the remarkable decrease in the irreversible dissolution of transition metals from LNCM cathodes, considering that Ca plays a crucial role in scavenging fluoride species. Consequently, recycling OS as a functional LNCM precursor is an innovative approach for enhanced cycling retention.