Metal Substrate Research Articles

Influence of Bond Coat Roughness on Adhesion of Thermal Barrier Coatings Deposited by the Electron Beam–Physical Vapour Deposition Process

Thermal barrier coatings (TBCs) are effective protective and insulative coatings on hot section components of turbine engines. The quality and subsequent performance of the TBCs are strongly dependent on the adhesion between the coating and the metal substrate. The adhesion strength of TBCs varies depending on the substrate materials and coating, the coating technique used, the coating application parameters, the substrate surface treatments, and environmental conditions. Therefore, the roughness of the substrate surface has a significant effect on the performance of the TBC system. In this work, the roughness and microstructure of the 7YSZ (7 wt.% yttria-stabilised zirconia) top coat under different bond coat roughness treatments were studied. The purpose of this paper was to investigate the influence of the roughness of the bond coat on the adhesion of 7YSZ TBCs prepared by the electron beam–physical vapour deposition (EB-PVD) process. The VPA (vapour phase aluminium) bond coat was deposited on Inconel 718 nickel superalloy substrate using the above-the-pack technique. The ceramic top coat was applied to the bond coat using the EB-PVD process. The dependence between the TBC coating roughness and the bond coat roughness was determined. Adhesion strength measurements were performed according to the ASTM C 633 standard test method. The highest adhesion value observed in the tensile adhesion tests was 105 MPa. However, it was not determined whether the surface roughness of the bond coat affects the adhesion of the 7YSZ top coat.

Docking interactions determine substrate specificity of members of a widespread family of protein phosphatases

How protein phosphatases achieve specificity for their substrates is a major outstanding question. PPM family serine/threonine phosphatases are widespread in bacteria and eukaryotes, where they dephosphorylate target proteins with a high degree of specificity. In bacteria, PPM phosphatases control diverse transcriptional responses by dephosphorylating anti-anti-sigma factors of the STAS domain family, exemplified by B. subtilis phosphatases SpoIIE, which controls cell-fate during endospore formation, and RsbU, which initiates the General Stress Response. Using a combination of forward genetics, biochemical reconstitution, and AlphaFold2 structure prediction, we identified a conserved, tripartite substrate docking interface comprised of three variable loops on the surface of the PPM phosphatase domains of SpoIIE and RsbU that recognize the three-dimensional structure of the substrate protein. Non-conserved amino acids in these loops facilitate the accommodation of the cognate substrate and prevent dephosphorylation of the non-cognate substrate. Together, single-amino acid substitutions in these three elements cause an over five-hundred fold change in specificity. Our data additionally suggest that substrate-docking interactions regulate phosphatase specificity through a conserved allosteric switch element that controls the catalytic efficiency of the phosphatase by positioning the metal cofactor and substrate. We hypothesize that this is a generalizable mechanistic model for PPM family phosphatase substrate specificity. Importantly, the substrate docking interface with the phosphatase is only partially overlapping with the much more extensive interface with the upstream kinase, suggesting the possibility that kinase and phosphatase specificity evolved independently.

Development of anti-corrosion coating with sandwich-like microvascular network for realization of self-healing and self-reporting properties based on coaxial electrospinning

Biomimetic microvascular networks prepared by coaxial electrospinning technology have attracted much attention as a novel form of carrier for encapsulating active substances. However, the poor interfacial bonding strength between traditional electrospinning materials and metal substrates limits its application in anti-corrosion coatings. Herein, a novel poly(vinyl alcohol) grafted phytic acid (PVA-PA) electrospinning solution was synthesized. And a sandwich-like microvascular network (SMN) was prepared by coaxial electrospinning technology, which used PVA-PA solution as the shell material, epoxy resin 51 (E51), tetraphenylethylene (TPE) and polyamide resin as the core materials, respectively. Owing to the high porosity of SMN, epoxy resin can be directly spin-coated on it to form a composite coating (PVA-PA/SMN/EP). It is proved that due to the strong chelation and coordination interaction between PA and mild steel, the pull-out adhesion of the PVA-PA/SMN/EP composite coatings on mild steel was increased by 0.92 MPa. In addition, by systematically optimizing the relative viscosity, miscibility, conductivity, and saturated vapor pressure between the two jets of the core solution and the shell solution in coaxial electrospinning, the microvascular structure of the coaxial electrospinning nanofibers was improved and the fluidity of the internal active substances was maintained. When the PVA-PA/SMN/EP composite coating generates microcracks, the active substances encapsulated in the SMN flow out, in which the three-dimensional crosslinked network formed by the curing of E51 and polyamide resin enhances the spatial interactions between TPE molecules, which results in TPE emitting a bright blue fluorescence. This work provides a new approach for the development of the next generation of smart anti-corrosion coatings.

Electrosynthesis of Transition Metal Coordinated Polymers for Active and Stable Oxygen Evolution

AbstractTransition metal coordination polymers (TM‐CP) are promising inexpensive and flexible electrocatalysts for oxygen evolution reaction in water electrolysis, while their facile synthesis and controllable regulation remain challenging. Here we report an anodic oxidation‐electrodeposition strategy for the growth of TM‐CP (TM=Fe, Co, Ni, Cr, Mn; CP=polyaniline, polypyrrole) films on a variety of metal substrates that act as both catalyst supports and metal ion sources. An exemplified bimetallic NiFe‐polypyrrole (NiFe‐PPy) features superior mechanical stability in friction and exhibits high activity with long‐term durability in alkaline seawater (over 2000 h) and anion exchange membrane electrolyzer devices at current density of 500 mA cm−2. Spectroscopic and microscopic analysis unravels the configurations with atomically distributed metal sites induced by d‐π conjugation, which transforms into a mosaic structure with NiFe (oxy)hydroxides embedded in PPy matrix during oxygen evolution. The superior catalytic performance is ascribed to the anchoring effect of PPy that inhibits metal dissolution, the strong substrate‐to‐catalyst interaction that ensures good adhesion, and the Fe/Ni−N coordination that modulates the electronic structures to facilitate the deprotonation of *OOH intermediate. This work provides a general strategy and mechanistic insight into building robust inorganic/polymer composite electrodes for oxygen electrocatalysis.

Local high temperature phenomena near the complex interfaces of thermal barrier coatings based on non-Fourier model

Thermal barrier coatings (TBCs) consist of a metal substrate (Sub), a bond coat (BC), and a ceramic top coat (TC). The ceramic coating is a porous dielectric layer with a significant relaxation time that cannot be ignored. In high-temperature environments, an irregularly shaped thermally grown oxide layer (TGO) forms between the BC and the TC. Therefore, using non-Fourier model to describe the thermal contact process of TBCs with complex interface can get more accurate results. However, it is difficult to obtain the analytical solution of this model. This paper introduces a finite volume method based on unstructured meshes to address the non-Fourier heat transfer process in the complex interfaces of multilayer TBCs. The gradient reconstruction technique is employed to calculate the cell derivatives on the surface. The method's reliability is confirmed through a comparison with a two-dimensional analytical solution. The results indicate that the thermal wave travels at a limited speed within the TC layer. After passing through the interface, the thermal wave travels very fast within the BC and Sub layers, due to the influence of thermal wave reflection and superposition, obvious local high temperature will be formed near the interface. In addition, the effects of thermal conductivity, relaxation time and interface shapes on the non-Fourier heat conduction process of TBCs are also discussed. The results of this paper are useful for the structural design and failure mechanism research in TBCs.

Electrosynthesis of Transition Metal Coordinated Polymers for Active and Stable Oxygen Evolution.

Transition metal coordination polymers (TM-CP) are promising inexpensive and flexible electrocatalysts for oxygen evolution reaction in water electrolysis, while their facile synthesis and controllable regulation remain challenging. Here we report an anodic oxidation-electrodeposition strategy for the growth of TM-CP (TM=Fe, Co, Ni, Cr, Mn; CP=polyaniline, polypyrrole) films on a variety of metal substrates that act as both catalyst supports and metal ion sources. An exemplified bimetallic NiFe-polypyrrole (NiFe-PPy) features superior mechanical stability in friction and exhibits high activity with long-term durability in alkaline seawater (over 2000 h) and anion exchange membrane electrolyzer devices at current density of 500 mA cm-2. Spectroscopic and microscopic analysis unravels the configurations with atomically distributed metal sites induced by d-π conjugation, which transforms into a mosaic structure with NiFe (oxy)hydroxides embedded in PPy matrix during oxygen evolution. The superior catalytic performance is ascribed to the anchoring effect of PPy that inhibits metal dissolution, the strong substrate-to-catalyst interaction that ensures good adhesion, and the Fe/Ni-N coordination that modulates the electronic structures to facilitate the deprotonation of *OOH intermediate. This work provides a general strategy and mechanistic insight into building robust inorganic/polymer composite electrodes for oxygen electrocatalysis.

Self-stacked small molecules for ultrasensitive, substrate-free Raman imaging in vivo.

Raman spectroscopy using surface-enhanced Raman scattering (SERS) nanoprobes represents an ultrasensitive and high-precision technique for in vivo imaging. Clinical translation of SERS nanoprobes has been hampered by biosafety concerns about the metal substrates used to enhance Raman signals. We report a set of small molecules with bis-thienyl-substituted benzobisthiadiazole structures that enhance Raman signal through self-stacking rather than external substrates. In our technique, called stacking-induced charge transfer-enhanced Raman scattering (SICTERS), the self-stacked small molecules form an ordered spatial arrangement that enables three-dimensional charge transfer between neighboring molecules. The Raman scattering cross-section of SICTERS nanoprobes is 1350 times higher than that of conventional SERS gold nanoprobes of similar particle size. SICTERS outperforms SERS in terms of in vivo imaging sensitivity, resolution and depth. SICTERS is capable of noninvasive Raman imaging of blood and lymphatic vasculatures, which has not been achieved by SERS. SICTERS represents an alternative technique to enhance Raman scattering for guiding the design of ultrasensitive substrate-free Raman imaging probes.

Enhancing Tribological Characteristics of Titanium Grade-5 Alloy through HVOF Thermal-Sprayed WC-Co Nano Coatings by TOPSIS and Golden Jack Optimization Algorithm.

Thermal spray coatings have emerged as a pivotal technology in materials engineering, primarily for augmenting the characteristics related to wear and tribology of metallic substrates. This study aimes to delve into applying High-Velocity Oxygen Fuel (HVOF) thermalsprayed WC-Co nanocoatings on Titanium Grade-5 alloy (Ti64). The coating process, utilizing nano-sized WC-Co powder, undergoes systematic optimization of HVOF parameters, encompassing the flow rate of carrier gas, powder feed rate, and nozzle distance. Experimental assessments via Pin-on-Disc (PoD) tests encompass Loss of Wear (WL), Friction Coefficient (CoF), and Frictional Force (FF). Later, an exhaustive optimization of responses is conductede using the Technique for Order Preference by Similarity to the Ideal Solution (TOPSIS) method and the golden jack optimization algorithm (GJOA). Outcomes show a substantial increase in WL, CoF, and FF with a rise in the carrier gas and powder feed rate. However, with increasing spraying distance of powder, the WL, CoF, and FF tend to lower due to higher bonding, which leads to increased wear resistance. The ideal parametric settings achieved from TOPSIS and GJOA are 245 mm of spray distance, 30 gpm rate of powder feed, and 11 lpm of carrier gas flow rate. The powder feed rate contributes 88.99% to the control action, as seen from ANOVA. The confirmation experiment presents that the WL, CoF, and FF output responses are 42.33, 27.97, and 9.38% less than the mean of experimental data. These results highlight the HVOF process in spraying WC-Co nanocoatings to fortify the durability and performance of Ti64 alloy that can be patented for diverse engineering applications.

A novel UV-curable composite coating with superior anti-corrosion and mechanical properties

The UV curing method is free from volatile organic compounds (VOC) and exhibits high curing efficiency. However, pore flaws and inadequate mechanical qualities after cure greatly hinder their utilization in metal anti-corrosion. Herein, layered double hydroxides (LDH) supported by molybdic acid and cerium ions were synthesized in situ on the sericite (SC) surface, enhancing the shielding, corrosion inhibition, resin compatibility, and cross-linking density of the coating. Compared with carbon steel immersed in a 3.5 wt% NaCl solution, the incorporation of SC/KH560@LDH reduced the corrosion current density (Icorr) from 2.001 × 10−5 A/cm2 to 7.883 × 10−6 A/cm2. Moreover, the low-frequency impedance of the UV-SC/KH560@LDH coating remained high at 1.939 × 1010 Ω·cm2 after 70 days of immersion in a 3.5 wt% NaCl solution. The excellent corrosion resistance of UV-SC/KH560@LDH can be attributed to the barrier properties of the filler, the chloride ion trapping, and the passivation effect. Furthermore, the UV-curable alkyd resin used in this work formed a chemical bond with the metal substrate, enhancing the mechanical properties of the coating. The adhesion strength of the UV-SC/KH560@LDH was measured at 11.50 MPa. The thickness loss (21.3 μm) of the UV-SC/KH560@LDH were minimal after 5000 cycles of wear. A new research concept for preparing the UV-SC/KH560@LDH with superior anti-corrosion and mechanical properties for carbon steel plate surfaces has been proposed to meet the demands of practical applications.

Electronic Oxide-Metal Strong Interactions (EOMSI) Localized at CeOx-Ag Interface.

Electronic oxide-metal strong interactions (EOMSI) refer to the electronic oxide-metal interactions (EOMI) between oxide adlayers and underlying metal substrate that is strong enough to stabilize supported oxide adlayers in a low-oxidation state, which individually is not stable under an ambient condition, from high temperature oxidation in air to a certain extent. Herein we report the deposition and electronic structure of CeOx adlayers on capping ligand-free cubic Ag nanocrystals, i.e., CeOx/Ag inverse catalysts. The EOMI occur via the charge transfer from Ag substrate to CeOx adlayers in the CeOx/Ag inverse catalyst, and the EOMSI are observed in the CeOx/Ag inverse catalyst with the average thickness of CeOx adlayers about 0.9 nm to exclusively form Ce2O3 adlayers stable against oxidation at 400 °C. As the thickness of CeOx adlayers increases, ceria adlayers with oxygen vacancies (CeO2-x) emerge and grow in the CeOx/Ag inverse catalysts, and the Ce3+/Ce4+ ratio decreases. Catalytic performance of CeOx/Ag inverse catalysts in the CO oxidation reaction is closely linked with the thickness and electronic structure of CeOx adlayers. These results demonstrate that the EOMSI and EOMI in the oxide/metal inverse catalysts are localized at the oxide-metal interface and sensitively vary with the thickness of oxide adlayers, offering a strategy of thickness engineering to tune electronic structures of oxide adlayers in oxide/metal inverse catalysts.

Remote vapor-phase dual alkali halide salts assisted quasi-van der Waals epitaxy of m-phase ZrO2 thin films with high dielectric constant and stable flexible properties

High-κ dielectric constant and wideband gap of ZrO2 material render it as an excellent candidate for transistor gate dielectric layers. However, current reported synthesis techniques suffer the problems of high precursor volatilization rate, ultrasmall grains with low dielectric constant, and high leakage current, which largely impede its application in electronic devices. Here, the quasi-van der Waals epitaxy growth of compact m-phase ZrO2 thin films has been developed, in which the stable supply of Zr source is realized by the tuned sublimation of ZrC powder with remote vapor-phase dual halide salts assistant. The formation of m-phase ZrO2 is due to the lower Gibbs free energy, in which the crystal nucleates at the etched hole edges of mica substrate, thus forming hexagonal shape polycrystal grains and merging as the continuous thin films. The microstructures and Raman spectrum characterization reveal the two dominated growth orientations and good crystal qualities, which indicate the uniform dielectric constant. The excellent growth reproducibility could be easily adapted to thin metal substrates, such as tungsten, molybdenum, and stainless steel, where the adhesion strength is strong because of the higher density of interfacial chemical bonding. Meanwhile, the metal–insulator–metal flexible capacitors show the high dielectric constant of 23–26 and low leakage current density of 10−4 A/cm2 at large voltage and only exhibit the decreased capacitance density of 7% after several hundred bending cycles. Our work paves a way to achieve the high-quality dielectric thin films on various substrates by the unique chemical vapor deposition design strategy.

Theoretical study on the electrochemical CO2 reduction performance of MoS2-supported Ni single atoms with transition metal substrate doping

In the context of increasing energy issues and climate change, the development of electrochemical CO2 reduction strategies using single atom catalysts (SACs) presents a viable solution by converting CO2 into high-value-added products. Transition metal dichalcogenides (TMDs) have emerged as the main candidates for SACs in electrocatalytic CO2 reduction reaction (CO2RR) catalysts. The regulation of the second coordination sphere of SACs is known to modulate their electronic structure and catalytic behavior. This study delves into the effect of transition metal-doped substrates on SACs. We employed spin-polarization density functional theory (DFT) to design a series of Ni/TM-MoS2 monolayer MoS2 materials, with transition metals (including Cr, Mn, Fe, Co, Ni, Cu, Ru, Rh, Pd, Ag, W, Re, Os, Ir, Pt and Au) substituting the Mo atoms and anchoring single atom Ni. Among them, six Ni/TM-MoS2 catalysts doped with Mn, Fe, Co, Ru, Rh, and Ir demonstrate enhanced CO2RR activity and selectivity when compared to unmodified Ni/MoS2. The Ni/Ru-MoS2 SAC exhibits the best catalytic activity and selectivity for formic acid production, with a limiting potential (UL) of -0.06 V. The incorporation of the metal-doped substrate lowers the work function of the catalyst, facilitating electron transfer and reaction progression. Furthermore, a volcanic relationship was observed between the work function and UL. This study provides strategic insights into the design and development of SACs, highlighting the potential for future modifications and applications.

Study on rapid growth and improved performance of superconducting YBa2Cu3O7-δ coated conductors assisted by transient liquid phase

This study employs a fluorine-free metal organic deposition method (FF-MOD), with transient liquid phase assistance, to expedite the growth (TLAG) of superconducting YBa2Cu3O7-δ (YBCO) thin films on LaMnO3 metal substrates. The research evaluates the phase formation and performance of YBCO films with varying proportions of preformed BaZrO3 (BZO) nanocrystals. The experimental results indicate that the optimal proportion for incorporating BZO nanocrystals is 5 %, leading to the YBCO film displaying critical current density at 77 K under zero-field conditions. This achievement marks a significant advancement in the rapid growth of YBCO films on metal substrates with enhanced current-carrying capacity. Additionally, the research assesses the changes in overall uniformity and microstrain of YBCO films after the addition of BZO nanocrystals, shedding light on the key factors contributing to performance enhancement and offering insights for future improvements. This investigation offers valuable insights for attaining high-speed, high-performance growth of superconducting YBCO coating conductors.

Electron-Beam-Induced Modification of N-Heterocyclic Carbenes: Carbon Nanomembrane Formation.

Electron irradiation of self-assembled monolayers (SAMs) is a versatile tool for lithographic methods and the formation of new 2D materials such as carbon nanomembranes (CNMs). While the interaction between the electron beam and standard thiolate SAMs has been well studied, the effect of electron irradiation for chemically and thermally ultrastable N-heterocyclic carbenes (NHCs) remains unknown. Here we analyze electron irradiation of NHC SAMs featuring different numbers of benzene moieties and different sizes of the nitrogen side groups to modify their structure. Our results provide design rules to optimize NHC SAMs for effective electron-beam modification that includes the formation of sulfur-free CNMs, which are more suitable for ultrafiltration applications. Considering that NHC monolayers exhibit up to 100 times higher stability of their bonding with the metal substrate toward electron-irradiation compared to standard SAMs, they offer a new alternative for chemical lithography where structural modification of SAMs should be limited to the functional group.

Multifunctional Ti3C2Tx-based epoxy composite coating towards intelligent response and corrosion/wear resistance

Questions remain about the unreasonable collocation of Ti3C2Tx and nanocontainers resulting in the performance degradation of multi-function Ti3C2Tx-based epoxy composite coating. Here, mesoporous SiO2 nanocontainers (SNT) containing both potassium thiocyanate and hexadecyl trimethyl ammonium bromide (CTAB) were loaded on MXene-based platform (SNT-on-MP) to achieve a novel epoxy coating (SNT-on-MP@EP) with the integrated functions of self-warning, self-healing, anti-corrosion and anti-wear. In the damaged area, the thiocyanate groups combined with Fe3+ ions to form a blood-red color display, and the formed coordination compound and CTAB as corrosion inhibitors were deposited on the metal substrate, thus showing intelligent response function. Besides, because of passive and active synergistic protection functions, the lowest-frequency impedance value of SNT-on-MP@EP maintained 5.74 × 107 Ω·cm2 after 4 weeks of exposure in salt water environment, which was increased by two orders of magnitude compared with pure epoxy coating. Under the reciprocating sliding friction, the wear rate of SNT-on-MP@EP reached 5.32 × 10−5 mm3/N·m, and was reduced by 58.29 %, owing to the formation of lubricant film at the friction interface and the enhancement of the deformation resistance of the coating. The reasonable collocation of SNT and Ti3C2Tx-based platform eliminated the problem of weak interaction between traditional inorganic nanocontainer and water-based epoxy coating, thus giving full play to the advantages of both.

Tribological properties of YG8/steel friction pair in an aqueous lubrication system with an ionic liquid: Experimental results and molecular dynamics simulations

In this work, an ionic liquid (G-RIC) with excellent lubricating performance was successfully prepared, and the tribological properties as an additive in glycerol-water solutions were explored. The results indicated that 2.0 % additive content can reduced the friction coefficient to below 0.1, leading to a decline in the wear volume of 76 %. Gray cast iron corrosion tests revealed that the additive exhibited excellent corrosion resistance. Quantum chemical calculations revealed that the anion RIC has a low energy gap (ΔE = 0.034 Ha), which implies that it is more prone to undergoing tribochemical reactions with the metal substrate under frictional heat. The synergistic action of the liquid lubrication layer, adsorption film, and friction protective film created an interface that easily shears.

Chirality-Induced Magnetic Polarization by Charge Localization in a Chiral Supramolecular Crystal.

The chirality-induced spin selectivity (CISS) effect is a fascinating phenomenon that correlates the molecular structure with electron spin-polarization (SP). Experimental procedures to quantify the spin-filtering magnitude have extensively used magnetic-field-dependent conductive AFM. In this work chiral crystals of imide-substituted coronene bisimide ((S)-CBI-GCH) are studied to explain the dynamics of the current-voltage I - V spectra and the origin of superimposed peaks are investigated. A dynamic voltage-sweep rate-dependent phenomenon can give rise to complex I - V curves. The redox group, capable of localization of charge, acts as a localized state that interferes with the continuum of the π - π stacking, giving rise to Fano resonances. A novel mechanism for dynamic transport is introduced, which provides insight into the origin of spin-polarized charge in crystallized CBI-GCH molecules after absorption on a metallic substrate, guided by transient charge polarization. Crucially, interference between charge localization and delocalization during transport may be important properties in understanding the magnetochiral phenomena observed by electrostatic force microscopy. Finally, it is observed that charge trapping sensitively modifies the injection barrier from direct tunneling to Fowler-Nordheim tunneling transport supporting nonlinearity in CISS for this class of molecules.

A study on the impact of liquid metal droplets onto metal and elastomer substrates

A study on the impact of liquid metal droplets onto metal and elastomer substrates

Effect of phytic acid/rust conversion layer on corrosion protection of rusty mild steel

In this study, a rust/phytic acid (rust/PA) conversion layer was prepared on rusty mild steel by dipping rusty steel panels into a phytic acid solution. After treating with phytic acid, the free phosphate group in the conversion layer chelated with Fe3+ and generated insoluble salt, which could form a new dense conversion layer. The dense rust/PA conversion layer effectively strengthened the interfacial bonding between the coatings and rusty metal substrate and exhibited good corrosion protection and defect healing abilities.

Predicting the Adhesive Layer Thickness in Hybrid Joints Involving Pre-Tensioned Bolts.

While most academic studies focus on the properties of cured joints, this research addresses the manufacturing process of hybrid joints in their uncured state. Hybrid joints that combine adhesive bonding with pre-tensioned bolts exhibit superior mechanical performance compared to exclusively bonded or bolted joints. However, the adhesive flow during manufacturing in hybrid joints often results in a nonuniform adhesive thickness, where obtaining an exact thickness is crucial for accurate load capacity predictions. This paper presents experiments involving three different adhesives, providing precise measurements of the adhesive layer thickness distribution, which served as a reference when evaluating and validating the subsequent numerical predictions. The numerical predictions were performed using computational fluid dynamics (CFD) to model the flow behavior of the adhesives during the bonding process and their interactions with the metal substrates. The CFD predictions of the adhesive layer thickness showed good agreement with the experimental data, with the relative differences between the average experimental and numerical thickness values ranging from 4.07% to 27.1%. The results were most accurate for the adhesive with sand particles, whose particles remained intact, ensuring that the adhesive's rheology remained unchanged. The results highlight the importance of the rheological behavior of the adhesive in the final distribution of the adhesive layer thickness, thereby expanding the understanding of these joints.