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BACKGROUND: The aim of this study is to evaluate the surface microhardness, surface chemical composition of bioactive restorative materials pre- and post- thermal aging. METHOD: A total of 200 disc-shaped samples were prepared by using the materials: Cention N, ACTIVA BioActive Restorative, Equia Forte HT Fil, Glass Fill glass carbomer cement (GCP), and Fuji II LC. Vickers microhardness test were used to measure surface hardness. Scanning electron microscopy-energy dispersive X-ray spectroscopy (SEM/EDS) was used to determine the characterization of the microstructures and elemental analysis of the materials. These measurements were repeated after thermal aging. One-Way ANOVA test, Bonferroni test and the Games-Howell test was used for data analysis. The significance level was accepted as 0.05. RESULTS: Cention N had the highest vickers microhardness value before thermal cycle. The highest fluoride ion ratio among the materials before thermal aging was detected in the Equia Forte HT Fil and Fuji II LC groups. While a decrease in fluorideF ion was detected in all groups except the Cention N group after thermal aging. It is observed that ACTIVA BioActive Restorative has a more microporous and rougher surface in the scanning electron microscopy image after the thermal cycle than in the image before the thermal cycle. CONCLUSIONS: The chemical properties of the materials and the properties of the filler particles may be related to the differences in the mechanical properties, surface characterizations and ion releases of the materials Thermal aging affected the microhardness, surface characteristics and elemental mass ratios of the studied materials. Alkasite bioactive materials are more similar to composite restorative materials and show better mechanical properties than other materials, but do not have the same effect on fluoride release. CLINICAL RELEVANCE: Most of the bioactive materials showed a decrease in the fluoride ion ratio after thermal aging, while no difference was found in the ion exchange of alkasite materials. Material selection should be made more carefully in caries-active individuals whose fluoride release is clinically important.
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Cimentos de Ionômeros de Vidro , Dureza , Teste de Materiais , Microscopia Eletrônica de Varredura , Espectrometria por Raios X , Propriedades de Superfície , Cimentos de Ionômeros de Vidro/química , Temperatura Alta , Resinas Compostas/química , Fluoretos/química , Fluoretos/análise , Materiais Dentários/química , Fatores de Tempo , Apatitas , Resinas SintéticasRESUMO
BACKGROUND: The temperature changes, chemical agents, and brushing activity that resin composite restorations are exposed to in the oral environment can cause changes in surface roughness. In this study, the aim was to investigate in vitro the clinical one-year surface roughness changes of different types of composites (flowable or conventional) from the same companies by subjecting them to immersion in solutions, brushing, and thermal cycling procedures to simulate intraoral conditions. METHODS: Four different resin composite brands were included in the study using both their conventional (Charisma Smart, 3M Filtek Ultimate Universal, Omnichroma, Beautifil II) and flowable resin composites (Charisma Flow, 3M Filtek Ultimate Flowable, Omnichroma Flow, Beautifil Flow Plus F00), giving 4 groups with 2 types of resin composite in each. 40 samples were prepared for each group/resin type, for a total of 320 samples. After initial surface roughness measurements by a mechanical profilometer, the samples were divided into 4 subgroups (n = 10) and immersed in solutions (distilled water, tea, coffee, or wine) for 12 days. The samples were then subjected to 10,000 cycles of brushing simulation and 10,000 cycles of thermal aging. Surface roughness measurements were repeated after the procedures. For statistical analysis, the 3-way analysis of variance and the Tukey test were used (p < 0.05). RESULTS: It was concluded that composite groups and types had an effect on surface roughness at time t0 (p < 0.001). At time t1, the highest surface roughness value was obtained in the Beautifil-conventional interaction. When the surface roughness values between time t0 and t1 were compared, an increase was observed in the Beautifil II and Beautifil Flow Plus F00, while a decrease was observed in the other composite groups. CONCLUSION: Composite groups, types, and solutions had an effect on the surface roughness of resin composites. After aging procedures, it was concluded that the Beautifil group could not maintain the surface structure as it exceeded the threshold value of 0.2 µm for bacterial adhesion.
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Café , Resinas Compostas , Teste de Materiais , Propriedades de Superfície , Escovação Dentária , Resinas Compostas/química , Água/química , Fatores de Tempo , Chá , Temperatura , Humanos , Materiais Dentários/química , Imersão , Metacrilatos/química , Técnicas In Vitro , Poliuretanos/química , Ácidos Polimetacrílicos/química , Polietilenoglicóis/química , Bis-Fenol A-Glicidil MetacrilatoRESUMO
In this study, two types of composites, polybutylene terephthalate (PBT) and epoxy resin (ER), reinforced with 20% of glass fiber (GF) are used as the comparative research objects. Their mechanical properties after thermal aging at 85~145 °C are evaluated by tensile strength and fracture morphology analysis. The results show that the composites have similar aging laws. The tensile strength of GF/PBT and GF/ER decrease gradually with the increase of aging temperature, while their elastic moduli are independent of the thermal treatment temperature. Scanning electron microscopy study of the fracture surface shows that separation of glass fiber from PBT and ER matrix becomes more obvious at higher aging temperature. The fibers on the matrix surface appear clear and smooth, and the whole pulled out GFs can be observed. As a main mechanical strength degradation mechanism, the deterioration of interface adhesion between the matrix and GF is discussed. A large difference in coefficients of thermal expansion of the matrix and GF is a main factor of the mechanical degradation.
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High exhaust temperature is an intrinsic nature of natural gas engines which underlies power de-rating and thermal aging of after-treatment system; therefore, this study integrates an organic Rankine cycle (ORC) system between engine and it's three-way catalyst (TWC) to address these challenges. ORC facilitates power output enhancement through exhaust energy recovery and alleviates thermal aging by reducing exhaust temperature. To estimate the effectiveness of this hypothesized system, a simulation-based investigation is performed. First, simulation models, including engine, TWC, and vehicle dynamic models, are built and validated by experimental data. According to the temperature characteristics of different TWCs, three scenarios, representing old, current, and prospective TWC technology, are formulated to estimate the ORC performance under Worldwide Harmonized Light Vehicles Test Cycle. Results show that ORC system can substantially alleviate the thermal damage caused by high exhaust temperature and extend TWC lifespan. It is estimated that over 98.5 % of thermal damage can be decreased by proper ORC setting, and the average TWC lifespan extension can be at least 55.4, making a reduced noble metal usage and cost of TWC. Meanwhile, with the decrease of the working temperature of TWC, ORC can recover exhaust energy under more road conditions, further improving the net power and shortening the payback period of extra ORC hardware costs. A reduction in the working temperature of TWC from 770.5 K to 618 K yields a 109 % enhancement in maximum power, coupled with a 62.30 % reduction in the payback period. These findings fully reflect the advantage of ORC-TWC coupling and indicate that ORC is supposed to be used more for the TWC with a low working temperature to maximize economic effectiveness. This study provides a novel pathway for thermal aging alleviation of TWC and a valuable reference for prospective studies on matching ORC with TWC under road conditions.
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The direct-drive selective compliance assembly robot arm (SCARA) is widely used in high-end manufacturing fields, as it omits the mechanical transmission structures and has the advantages of high positioning accuracy and fast movement speed. However, due to the intensifying dynamic coupling problem of structures in the direct-drive SCARA, the permanent magnet synchronous motors (PMSMs) located at the joints will take on nonstationary loads, which causes excessive internal temperature and reduces the lifetime of PMSMs. To address these issues, the lifetime prediction of PMSMs is studied. The kinematic and dynamic models of the SCARA are established to calculate the torque curve required by the PMSM in specific typical motion tasks. Additionally, considering thermal stress as the main factor affecting lifetime, accelerated degradation tests are conducted on insulation material. Then, the reliability function of the PMSM is formulated based on the accelerated degradation model. Based on the parameters and working conditions of the PMSM, the temperature field distribution is obtained through simulation. The maximum temperature is used as the reference temperature to conduct reliability evaluation and lifetime prediction of the PMSM. The research results show that for a typical point-to-point task, the PMSM can run for 102,623 h while achieving the reliability requirement of 0.99.
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To use polylactic acid in demanding technical applications, sufficient long-term thermal stability is required. In this work, the thermal aging of polylactic acid (PLA) in the solid phase at 100 °C and 150 °C is investigated. PLA has only limited aging stability without the addition of stabilizers. Therefore, the degradation mechanism in thermal aging was subsequently investigated in more detail to identify a suitable stabilization strategy. Investigations using nuclear magnetic resonance spectroscopy showed that, contrary to expectations, even under thermal aging conditions, hydrolytic degradation rather than oxidative degradation is the primary degradation mechanism. This was further confirmed by the investigation of suitable stabilizers. While the addition of phenols, phosphites and thioethers as antioxidants leads only to a limited improvement in aging stability, the addition of an additive composition to provide hydrolytic stabilization results in extended durability. Efficient compositions consist of an aziridine-based hydrolysis inhibitor and a hydrotalcite co-stabilizer. At an aging temperature of 100 °C, the time until significant polymer chain degradation occurs is extended from approx. 500 h for unstabilized polylactic acid to over 2000 h for stabilized polylactic acid.
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The development of offshore wind farms requires robust bonding solutions that can withstand harsh marine conditions for the easy integration of secondary structures. This paper investigates the durability performance of two adhesives: Sikadur 30 epoxy resin and Loctite UK 1351 B25 urethane-based adhesive for use in offshore wind environments. Tensile tests on adhesive samples and accelerated aging tests were carried out under a variety of temperatures and environmental conditions, including both dry and wet conditions. The long-term effects of aging on adhesive integrity are investigated by simulating the operational life of offshore installations. The evolution of mechanical properties, studied under accelerated aging conditions, provides an important indication of the longevity of structures under normal conditions. The results show significant differences in performance between the two adhesives, highlighting their suitability for specific operating parameters. It should also be noted that for both adhesives, their exposure to different environments (seawater, distilled water, humid climate) over a prolonged period showed that (i) Loctite adhesive has a slightly faster initial uptake than Sikadur adhesive, but the latter reaches an asymptotic plateau with a lower maximum absorption rate than Loctite adhesive; and (ii) a progressive deterioration in the tensile properties occurred following an exponential function. Therefore, aging behavior results showed a clear correlation with the Arrhenius law, providing a predictive tool for the aging process and the aging process of the two adhesives followed Arrhenius kinetics. Ultimately, the knowledge gained from this study is intended to inform best practice in the use of adhesives, thereby improving the reliability and sustainability of the offshore renewable energy infrastructure.
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CONTEXT: Thermal aging significantly deteriorates the mechanical properties and service performance of epoxy resins used for the high-voltage bushing. Current studies on the thermal aging behavior of epoxy resins mainly focus on experimental observations. However, an in-depth understanding of the mechanism of thermal aging of epoxy resins requires the monitoring of structural evolution of epoxy resins during thermal aging at the molecular level. To thoroughly analyze the intrinsic factors affecting structural evolution and the effect of thermal aging on the mechanical properties of epoxy resin for high-voltage bushing, epoxy resin models with different crosslinking degrees were established and thermal aging treatments at various temperatures and time periods were carried out by molecular dynamics simulation. It was found that the tensile strength of the epoxy resin was enhanced with the increase of the crosslinking degree, which was related to the elevation of the proportion of C-N and O-H bonds in its structure. With the increase of thermal aging temperature, the tensile strength of the epoxy resin decreased, which was related to the formation of weak bonds. At the early stage of thermal aging and after a period of high-temperature thermal aging, the strength of epoxy resin significantly decreases. The thermal aging of the epoxy resin is accelerated under external loading. In addition, the crosslinking degree and curing agent also affect the thermal aging resistance of epoxy resins. The results of this study can provide guidance for predicting and improving the thermal aging resistance of epoxy resins. METHODS: Materials Studio was used to construct molecular models and complete crosslinking reactions. DGEBA and 44DDS (or 33DDS) were mixed at a ratio of 2:1, followed by crosslinking reaction. During this process, the Nose method was used to control temperature, the Berendsen method was used to control pressure, and the polymer consistent force field (PCFF) was used to control the motion and force of atoms. Isobaric-isothermal ensemble (NPT ensemble) was used to heat up epoxy resin models to various thermal aging temperatures of 400 K, 500 K, 600 K and 700 K. The models were maintained at these temperatures for different thermal aging times of 100 ps, 200 ps, 300 ps, 400 ps, 500 ps, 600 ps, 700 ps and 800 ps. Afterwards, the models were cooled down to 300 K and subjected to uniaxial tensile testing at this temperature with a strain rate of 1 × 109 s-1. The structural configurations and stress-strain data during the tensile process were recorded. The flow stress of the material was derived by counting the average stress in the 20-50% strain interval.
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Objetivo: Cuando las resinas compuestas son expuestas a procesos de envejecimiento naturales en boca, como es el ciclaje térmico, pueden sufrir un deterioro en sus propiedades ópticas. El objetivo de este estudio fue evaluar la influencia del envejecimiento térmico sobre la estabilidad del color de dos resinas compuestas. Materiales y métodos: Se confeccionaron 120 pas- tillas de resinas compuestas, divididas en dos grupos: uno de resina Spectra Smart (n=60) y otro de resina Filtex Z350 XT (n=60). Estas muestras fueron sometidas a distintos regíme- nes de ciclaje térmico de 0, 10.000, 20.000 y 30.000 ciclos con temperaturas de entre 5 ºC +/- 2 ºC y 55 ºC +/- 2 °C. Los parámetros de color CIE L*a*b* de cada muestra se mi- dieron con un espectrofotómetro antes y después del proceso de envejecimiento. Las diferencias de color se calcularon me- diante la fórmula CIELAB (ΔE). Los datos fueron analizados estadísticamente usando la prueba no paramétrica de Kruskal Wallis y de U-Mann Whitney. Resultados: Los distintos regímenes de termociclado produjeron cambios de color estadísticamente significativos en ambos materiales. El material que tuvo menor estabilidad cromática fue Spectra Smart aunque sin diferencias estadísti- camente significativas. Conclusión: El envejecimiento térmico simulado a tres años afecta la estabilidad de color de las muestras, tanto de las resinas Spectra Smart, como de Filtex Z350 XT, sin alcanzar los valores que clínicamente determinarían la necesidad del reemplazo de las restauraciones (AU)
Aim: When composite resins are exposed to natural ag- ing processes in the mouth, such as the thermal cycling, they may suffer a deterioration in their optical properties. The aim of this study was to evaluate the influence of thermal aging on the color stability of two composite resins. Materials and methods: 120 composite resins tablets were made, divided into two groups: one of Spectra Smart res- in (n=60) and another of Filtex Z350 XT resin (n=60). These were subjected to different thermal cycle regimes of 0, 10,000, 20,000 and 30,000 cycles with temperature between 5 °C +/- 2 °C and 60 °C +/- 2 °C. The CIE L*a*b* color parameters of each sample were measured with a spectrophotometer before and after the aging process. Color differences were calculat- ed using the CIELAB formula (ΔE). The data were statisti- cally analyzed using the non-parametric Kruskal Wallis and U-Mann Whitney tests. Results: The different thermocycling regimes produce statistically significant color changes in both materials. The material that had the least chromatic stability was Spectra Smart, although without statistically significant differences. Conclusion: Simulated 3 year thermal aging affects the color stability of the samples, both Spectra Smart resins and Filtex Z350 XT, without reaching the values that would clini- cally determine the need to replace the restorations (AU)
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Termodinâmica , Resinas Compostas/química , Temperatura Alta/efeitos adversos , Espectrofotometria/métodos , Teste de Materiais/métodos , Interpretação Estatística de DadosRESUMO
CO and HCHO are the main pyrolysis gases in long-term running dry-type reactors, and thus the diagnosis of thermal insulation faults inside such devices can be realized by sensing these gases. In this paper, a single Au atom-decorated WS2 (Au-WS2) monolayer is proposed as an original sensing material for CO or HCHO detection to evaluate the operation status of dry-type reactors. It was found that the Au atom prefers to be adsorbed at the top of the S atom of the pristine WS2 monolayer, wherein the binding force is calculated as -3.12 eV. The Au-WS2 monolayer behaves by chemisorption upon the introduction of CO and HCHO molecules, with the adsorption energies of -0.82 and -1.01 eV, respectively. The charge density difference was used to analyze the charge-transfer and bonding behaviors in the gas adsorptions, and the analysis of density of state as well as band structure indicate gas-sensing mechanisms. As calculated, the sensing responses of the Au-WS2 monolayer upon CO and HCHO molecule introduction were 58.7% and -74.4%, with recovery times of 0.01 s and 11.86 s, respectively. These findings reveal the favorable potential of the Au-WS2 monolayer to be a reusable and room-temperature sensing candidate for CO and HCHO detections. Moreover, the work function of the Au-WS2 monolayer was decreased by 13.0% after the adsorption of CO molecules, while it increased by 1.2% after the adsorption of HCHO molecules, which implies its possibility to be a work-function-based gas sensor for CO detection. This theoretical report paves the way for further investigations into WS2-based gas sensors in some other fields, and it is our hope that our findings can stimulate more reports on novel gas-sensing materials for application in evaluating the operation conditions of dry-type reactors.
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The evolution of the microstructure and the mechanical properties of a 15-6 martensite precipitated hardened (15-6 PH) stainless steel after thermal treatment and long-term aging at 480 °C were investigated. Compared with 17-4 PH steel, the content of Cr decreased and Ni increased in the newly developed 15-6 PH steel; therefore, reversed austenite formed after thermal treatment at 620 °C of the solution-treated 15-6 PH steel. Although the reversed austenite may reduce the strength of the steel, it is very beneficial for the inhibition of the aging brittleness of the steel. During the accelerated thermal aging at 480 °C, the Cu-rich phase gradually coarsened, and its crystal structure changed, while the reversed austenite phase sightly increased and the Charpy impact energy maintained a rather high value. The increase of the reversed austenite content can offset the reduction of the strengthening effect of the Cu-rich phase and therefore maintain an excellent impact property of the material after thermal aging.
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PURPOSE: To evaluate the metameric disparities among monolithic zirconia materials with differing yttrium compositions across various lighting conditions. MATERIALS AND METHODS: Thirty-six square-shaped zirconia samples measuring 10 × 10 × 0.5 mm were prepared from monolithic zirconia materials with three different yttrium contents. A 0.2 mm thick layer of polymerized dual-polymerizable self-adhesive resin cement was created using a silicone mold with the same dimensions as the prepared zirconia specimens. To evaluate metamerism, color measurements were conducted using a spectrophotometer device on a neutral gray background in a color measurement cabinet that offers four different illumination environments. All samples underwent aging by subjecting them to 10000 thermal cycles using a thermal cycle tester. Following thermal aging, color measurements were taken once more, and the data were recorded using the CIE L*, a*, b* color system. Two-way ANOVA and Post-hoc Bonferroni tests were employed to analyze the data. RESULTS: It was observed that there was no statistical difference among the color measurements made in different illumination environments of the monolithic zirconia ceramics used to evaluate metamerism (P > .05). This observation remained consistent both before and after thermal aging. After thermal aging, the color of monolithic zirconia materials exhibited a tendency towards red and yellow hues, accompanied by a decrease in brightness levels. CONCLUSION: It can be stated that different illumination conditions did not affect the metamerism of monolithic zirconia materials, but there was a color change in monolithic zirconia materials after a thermal aging period equivalent to one year.
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Development of load-bearing fiber reinforced plastic (hereinafter referred to as FRP) composite structures in civil engineering, exploited under high temperatures, such as industrial chimneys and gas ducts, requires the knowledge of their long-term behavior under constant and cyclic mechanical and temperature loads. Such conditions mean that the viscoelasticity of FRP should be considered along with the thermal aging effect. This research is devoted to the effects of thermal aging on the viscoelastic behavior of polymers. Two sets of experiments were conducted: creep tensile tests and cyclic heating in a constrained state. The Kelvin-Voigt viscoelasticity model was used to determine the rheological parameters of binder from experimental creep curves. Cyclic heating was used to compare the behavior of normal and thermally aged binders and to evaluate the possibility of temperature stress accumulation. Fourier-transform infrared spectroscopy was used for polymer's structural changes investigation. Both tests showed that non-aged glassed polymer (hereinafter referred to as GP) was prone to viscoelastic behavior, while the thermally aged GP lost viscosity and worked almost perfectly elastic. It was assumed that long heat treatment had caused changes in the inner structure of the GP, reducing the number of weak bonds and increasing the number of elastic ones. Therefore, the results show that the designing of FRP structures, exploited under thermomechanical load, requires using the elastic model while taking into account the properties of FRP after long-term heat treatment.
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A multi-analytical approach was used to investigate the effect of thermal aging on the microstructure and mechanical properties of ER308L/Z2CND18.12N2. The results demonstrated that fractures occurred preferentially on the ER308L side. Z2CND18.12N2 exhibited superior fracture toughness compared to ER308L regardless of thermal aging time. The ultimate tensile strength significantly increased from 564.5 MPa in the unaged condition to 592.7 MPa to MPa after thermal aging and the fracture mode changed from ductile fracture into a ductile + quasi-cleavage fracture. The fusion zone (FZ) with the chemical composition gradient was about 40 µm from the Z2CND18.12N2 to ER308L. After thermal aging, spinodal decomposition and G-phase precipitation were observed for the first time in the ferrite phase of the FZ. Moreover, the hardness presented the following trend: FZ > ER308L > Z2CND18.12N2. The hardness of the ferrite phase dramatically increased from 6.13 GPa in an unaged condition to 8.46 GPa in a 10,000 h aged condition.
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BACKGROUND: This study aimed to investigate different surface treatments thought to increase the bond strength between zirconia ceramic and adhesive resin cement. METHODS: The samples were prepared in 15 × 10 × 2 mm dimensions by cutting off monolithic zirconia ceramic blocks (Incoris TZI; Sirona, Germany). Surface roughness measurements were made with a profilometer, the average surface roughness (Ra1) was recorded, and five different surface treatments were applied. Group 1: Control group. No surface treatment was applied. Group 2: Sandblasted with Al2O3 under pressure of 50 µm. Group 3: Sandblasted with 30 µm Al2O3 - SiOx under pressure, then tribochemical silica coating, silane bonding agent, and ceramic primer were applied. Group 4: Samples were etched in a hot acid solution containing methanol, HCl, and chloride at 100 °C. Group 5: Samples were coated in a solution containing Grade C Aluminum Nitrite at 75 °C for 15 Sects. 12,000 thermal aging was carried out to all samples. Then, samples were bonded to a composite surface (Filtek Z250) with two different types of adhesive cement (Panavia F 2.0, Rely X U200) (n = 10). A load was applied to the samples attached to the Universal Test Device for the SBS, and the SBS was recorded. The surface roughness measurements of all samples were made again, and the average surface roughness Ra2 was recorded. The data was analyzed with a two-way ANOVA test. Bonferroni correction was used for multiple comparisons of the groups. p = 0.005 was accepted as the statistically significant value. RESULTS: There was no statistically significant difference between the groups in the Ra1 measurements (p = 0.031). There was a statistically significant difference between the Ra2 values of Groups 4 and 5 and the Ra2 values of Groups 1,2 and 3 in the Ra2 measurements (p < 0.001). There was no statistically significant difference between the SBS values of the groups (p > 0.005). Also, there was no statistically significant difference in the SBS values of all groups for the two different cements tested (p > 0.005). CONCLUSIONS: None of the surface treatments applied to monolithic zirconia ceramic samples increased the SBS between ceramic and adhesive resin cement.
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Colagem Dentária , Cimentos de Resina , Humanos , Cimentos de Resina/química , Cimentos Dentários , Resistência ao Cisalhamento , Cerâmica/química , Propriedades de Superfície , Teste de Materiais , Análise do Estresse DentárioRESUMO
With the rapid iteration of microsystem integrated technology, the miniaturization of electronic devices requires packaging materials with higher reliability. In this work, the microstructure evolution and mechanical properties of novel epoxy composite SAC305 solder joints were studied after isothermal aging to evaluate the enhanced effect of epoxy addition. The thickness variation and morphological evolution of the interfacial layer were analyzed. The results showed that, as the aging time was prolonged, the Cu6Sn5 interfacial layer remarkably coarsened and Cu3Sn compounds formed between the Cu6Sn5 layer and Cu pad due to the continuous atomic diffusion. Compared with the monolithic joint, the epoxy composite SAC305 joints had a lower overall IMC growth rate during aging, closely related to the initial morphologies of the interfacial layers. The shear test results showed an apparent decrease in the shear forces of all the solder joints as the aging time increased. Nevertheless, because of the extra mechanical support provided by the epoxy layer, the epoxy composite joints demonstrated notably enhanced mechanical properties. After 1000 h aging treatment, the shear force of SAC305 joints containing 8 wt.% epoxy was 26.28 N, showing a 24.08% increase over the monolithic joint. Cu-Sn IMCs were detected on the shear fracture of the monolithic joint after 1000 h aging, indicating the fracture occurred near the interface and displayed a ductile/brittle mixed fracture. Concerning the epoxy composite joints, cracks were still initiated and extended within the solder bulk, demonstrating a noticeable enhancement in ductility due to the addition of epoxy.
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With the acceleration of the construction of sponge cities in China, porous asphalt pavement (PA) is has been widely used. High-viscosity asphalt (HVA) is the core material in building PA because it has good rheology properties, which can provide good raveling and rutting resistance. However, due to the open-graded structure of PA, HVA was more susceptible to rapid aging, which significantly affects the durability of PA. To investigate the thermal aging effect on the rheological properties of self-modified HVA (SHVA), five types of asphalts were aged using a rolling thin film oven (RTFO) and pressure aging vessel (PAV). Then, rheological tests were adopted, such as temperature sweep test (TS), repeated creep and recovery test (RCR), and bending beam rheometer test (BBR). The results indicate that during the aging process, the oxidation-induced hardening effect of neat asphalt and the degradation-induced softening effect of the modifier changes the rheology properties of HVA significantly. As the aging progresses, the contribution of the modifiers of HVA to anti-aging performance is greatly reduced. At high temperatures, HVA demonstrates better anti-aging performance than conventional styrene-butadiene-styrene (SBS)-modified asphalt (Guo Chuang, GC). The change of the high-temperature rheological indices of the two HVA types (SHVA and TAFPACK-super HVA (TPS)) showed a smaller activation energy index (EAI), a more considerable viscous component of binder creep stiffness (Gv), and more minor accumulated stain (racc), indicating a more significant anti-short-term and long-term aging performance, which is beneficial to the high-temperature performance of asphalts. However, the changes in low-temperature rheological properties do not align with those in high-temperature rheological properties after long-term aging. The BBR test results reveal that TPS exhibits worse low-temperature performance than GC and SHVA. During the thermal aging process, the contribution rate of the modifiers in SHVA against RTFO and PAV aging is higher than that of the modifiers in TPS, which contributes to the superior anti-aging property. Overall, SHVA demonstrates the best anti-aging performance among the five asphalts tested.
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Currently, the quest for more renewable and biodegradable materials is a scientific priority to address the problems of petroleum-based plastics are difficult to degrade. In this work, cellulose nanocrystals (CNC) have been used as a template and four morphologies of CNC-ZnO nanocomposites were prepared via a hydrothermal method, and CNC-ZnO/polylactic acid (PLA) composite films were obtained by solution casting. We find that CNC-ZnO nanocomposites as heterogeneous nucleating agents improved the crystallinity and the film with flower-like CNC-ZnO was improved by 2.4 %. Ea required for thermal degradation of the PLA films decreased to 66-81 % of that of neat PLA, calculated by the Kissinger method, the Friedman method, and the Flynn-Wall-Ozawa (FWO) method. The R2 model was the solid degradation mechanism of the PLA films, analyzed through the Coats-Redfern method and the Criado method. The H-bond content of the composite films was significantly reduced after thermal aging at 150 °C. We found that three-dimensional CNC-ZnO (ZnO-3) made more prominent contributions to the crystallization, thermal degradation, and thermal aging of PLA films than other dimensional. The thermal properties can be regulated by the dimension, size, and apparent morphology of CNC-ZnO nanoparticles.
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The effects of thermal aging at 85~145 °C in air on the tensile and flexural mechanical properties of 20% glass fiber (GF)-reinforced commercial grade polybutylene terephthalate (PBT) composites were studied. The results showed that as the aging temperature increased, the tensile and flexural strength of the GF/PBT composites significantly decreased. However, the elastic modulus of the composites was almost independent of aging. As the aging temperature increased, the separation between GF and the PBT matrix became more pronounced, and the fibers exposed on the surface of the matrix became clearer and smoother, indicating a decrease in interfacial adhesion between the PBT matrix and GF. The reason for this decrease in strength and brittle fracture of composites is the interface damage between the GF and PBT matrix caused by the difference in their thermal expansion coefficients during thermal aging.
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Ni-xCu/Sn soldering joints were aged at 200 °C, and the microstructure evolution and mechanical properties during the solid-state reaction were studied under shear loading. Results showed that the intermetallic compounds (IMCs) exhibited a Cu content-dependent transformation from the (Ni,Cu)3Sn4 phase to the (Cu,Ni)6Sn5 phase at the Ni-xCu/Sn interface. Furthermore, a Cu3Sn layer was observed exclusively at the Cu/Sn interface. The shear strength of the soldering joints after thermal aging exhibited an initial decrease followed by an increase, except for a significant enhancement at the Cu content of 60 wt.%. In addition, the evolution law of mechanical properties and failure mechanism of the thermal aging joints were elucidated based on the fracture microstructure and the fracture curve of the joints.