Loose Layer Research Articles

Failure mechanisms of multilayer TiN films based on mechanical properties of film and substrate

The poor adhesion, which is related to the mechanical properties of the substrate and film, leads to the film peeling off from the substrate and failure. In this study, TiN films with various structure were prepared on Ti6Al4V titanium alloy (TC4), 316L stainless steel (316L), 4Cr5MoSiV1 hot work die steel (H13), and W6Mo5Cr4V2 high-speed steel (W6) by adjusting the discharge currents using a hot-wire plasma-enhanced magnetron sputtering rig. The morphologies of the single-layer TiN films varied from loose to dense and ductile to brittle, and the nanohardness and elastic modulus increased as the hot-wire discharge current increased. The morphologies, nanohardnesses, and elastic moduli of the multilayer TiN films gradually approached those of the dense TiN single-layer films as the thicknesses of the top dense layers increased. The results, both by numerical simulation and experimental tests, revealed that the interfacial tensile stress and surface strain of a TiN/substrate system increased as the elastic modulus differences between TiN and its substrate increased, resulting in a serious TiN film elastic and plastic deformation asynchrony and poor film–substrate adhesion. The loose layer between the top dense TiN layer and its substrate acts as a buffer because the elastic modulus of the loose layer is in the middle, higher than that of the substrate but lower than that of the top dense layer. For TiN/TC4 or 316L with large differences in elastic moduli, loose/dense thickness ratios of 1:2 or 1:4 for the multilayer TiN films were sufficient to improve their adhesion. For TiN/H13 or W6, with small elastic modulus differences, a ratio of 1:4 was sufficiently large and may not be necessary.

Low-maintenance anti-scaling of nanofiltration pretreated by bipolar-induced electrolysis for decentralized water supply

Nanofiltration (NF) offers an effective solution to ensure a decentralized water supply. However, its reliance on dosing for pre-precipitation and anti-scaling severely complicates its maintenance, adding to its cost and limiting its application, especially in rural areas. In this study, a bipolar-induced electrolysis (BIE) pretreatment method was developed to reduce the NF membrane scaling potential without the need for additional reagents. The water flux of the BIE-NF increased by 24.2 ± 6.5 % compared to traditional NF. This benefits from the synergistic effects of electrocoagulation (EC) and electro-precipitation (EP) of BIE to remove hardness ions (36.8 ± 0.7 g CaCO3 m−2 h−1), 26.2 ± 2.6 % and 16.1 ± 4.7 % faster than that of traditional EP and EC, respectively, exhibiting robust resistance to the interfering ions and organics. The unit energy consumption of BIE was only 18.9 ± 1.0 kWh/(kg CaCO3), 11.8 ± 1.9 % and 67.0 ± 1.4 % lower than that of EP and EC, respectively. After BIE electrolysis, the Ca, humic acid, and Mg contents were dramatically reduced, and a uniformly loose fouling layer formed on the NF membrane, demonstrating alleviated membrane scaling. Remarkably, BIE softening demonstrated its stability and feasibility in sustaining 120.0 m3/d of drinking water to rural populations without requiring additional reagents or manual maintenance, minimizing the operation and maintenance cost to 5.1 US cents/m3 water, 29.0 % lower than the cost of conventional dosing pretreatment. This study offers a low-cost and sustainable method for water supply through decentralized membrane purification.

Risk assessment of land subsidence based on GIS in the Yongqiao area, Suzhou City, China.

This study focuses on the Yongqiao District in Suzhou City, Anhui Province, China, aiming to analyze the current situation of ground settlement and its influencing factors in the area. The selected risk indices include settlement rate, cumulative settlement amount, groundwater level drop funnel, thickness of loose sediment layer, thickness of soft soil layer, and the number of groundwater extraction layers. Additionally, vulnerability indices such as population density, building density, road traffic, and functional zoning are considered. An evaluation index system for assessing land Subsidence risk was established. The risk evaluation of land Subsidence was conducted using the Hierarchical analysis-composite index method and ArcGIS spatial analysis, The evaluation results show that the area of higher risk area is about 2.82 km2, accounting for 0.96% of the total area, mainly distributed in the area of Jiuli village, Sanba Street. The middle risk area is distributed around the higher area, with an area of about 9.18 km2, accounting for 3.13% of the total area. The lower risk areas were distributed in most of the study area, covering an area of 222.24 km2, accounting for 75.82% of the total area. The low risk assessment area is mainly distributed in Bianhe Street and part of Zhuxianzhuang Town, with an area of about 58.88 km2, accounting for 20.09% of the total area. The findings of this study are not only crucial for informing local policies and practices related to land use planning, infrastructure development, and emergency response but also enhance our understanding of the complexities of land Subsidence processes and their interactions with human activities, informing future research and practice in environmental risk assessment and management.

Positively charged nanofiltration membranes with gradient structures for enhancing separation properties

Creating a gradient structure in a separation layer is an effective approach for enhancing separation performance of thin film composite membranes. Here we present the preparation of a positively charged nanofiltration membrane with a gradient structure. An inner layer consisting of a loose polyester separation layer with large pores was formed through the interfacial polymerization (IP) reaction between triethanolamine (TEA) and trimesoyl chloride (TMC). And a dense and thin top layer composed of a polyamide separation layer was obtained by secondary interfacial polymerization (SIP) reaction using polyethyleneimine (PEI) along with unreacted TMC and residual acyl chloride groups of IP reaction. The influences of TEA concentration, PEI concentration and SIP time on the physicochemical properties and separation performances of the membrane were systematically analyzed. Our results show that the presence of the gradient structure optimized mass transfer pathways and reduced mass transfer resistance, resulting in significantly improved permeability of 13.0 ± 0.5 L·m−2·h−1·bar−1 (over 3 times compared with control-PEI), high MgCl2 rejection of 91.7 ± 0.6 %, and an excellent stability and anti-fouling performance. Our work provides valuable insights and guidance for developing high-performance positively charged NF membrane with gradient structures.

An investigation of the filtration performance and mechanism of oil-solid mixed particles on filter materials with different wettability

In the process of air filtration, filter materials may encounter oil-solid mixed particles from various sources such as industry and household, and the influence of filter material with different wettability on the filtration performance of oil-solid mixed particles has not been fully reported. The objective of this study was to prepare filter materials with varying wettability properties and investigate their filtration performance for oil-solid mixed particles with diverse oil contents. In this study, four filter materials were prepared using the impregnation method, exhibiting 0° (superoleophilic), 46° (oleophilic), 90° and 122° (oleophobic) oil contact angles. The oil-solid mixed particles with varying oil contents were loaded on the four different filter materials. The loading behavior of the filter materials was characterized from two aspects: macroscopic loading behavior (changes in pressure drop and DHC) and microscopic particle deposition behavior. The results demonstrated that, under the conditions of 25% and 50% oil content, the enhanced liquid bridge force between the oil-solid mixed particles on the oleophobic filter material facilitated the formation of a loose and porous cake layer structure compared with other filter materials, resulting in a lower growth rate of pressure drop and a higher dust holding capacity (DHC). However, in 75% and 100% oil content environments, the superoleophilic filter material owned a remarkably high affinity for oil particles compared with other filter materials, leading to the gradual formation of an oil film structure on the filter material, yielding lower the growth rate of pressure drop and higher DHC. These findings shed light on the mechanism of particle deposition under diverse filtration conditions and are applicable to the filtration of various oil-solid mixed particles over a wide range of oil contents.

Insights into the role of H2O2 on corrosion behavior of NiCu low alloy steel in simulated Beishan groundwater

Steel containers used for geological disposal of high-level radioactive waste will be gradually thinned or even perforated due to corrosion, which will lead to radiolysis of nuclides when they contact with infiltrated groundwater and produce H2O2. This work focused on investigating the influence of H2O2 concentration (0%, 0.001%, 0.01%, 0.1% and 1% by volume) on the corrosion behavior of NiCu low alloy steel as the candidate material for containers was comparatively studied by combining corrosion weight loss test, corrosion product analysis, morphology characterization, thermodynamic analysis and electrochemical measurements. As [H2O2] = 0.001%, H2O2 inhibited the formation of γ-FeOOH and enhanced the compactness of rust layer, which effectively blocked the migration of aggressive ions and slowed down the cathodic reduction reaction of rust, thus improving the corrosion resistance of NiCu steel. With the increase of [H2O2] (0.01%→1%), the cathodic process of NiCu steel corrosion was promoted by the increase of dissolved oxygen involved in cathodic depolarization. Meanwhile, the relative content of Fe3O4 in the rust increased, while Fe6(OH)12SO4 and Fe6(OH)12CO3 decreased obviously, which led to the loose and porous rust layer, thus accelerating the corrosion of NiCu steel.

Accelerated corrosion of 70/30 copper-nickel alloys in sulfide-polluted seawater environment by sulfide

The effect of sulfides on the pitting corrosion behavior and film chemistry of 70/30 copper-nickel alloys in aerated seawater was investigated. Sulfides in seawater prevent the formation of protective oxides on the surface of the alloy and alter the morphology and composition of the corrosion products. It results in the corrosion product film consisting of the double layer structure of the loose and porous sulfide-containing outer layer and the dense inner layer. This double-layer structure of the corrosion product film can't alleviate corrosion, but instead accelerates the development of pitting corrosion. The statistical analysis method is used to study the corrosion process of 70/30 copper-nickel alloy in sulfide-containing environment. This work records the trend of pitting corrosion towards the horizontal and longitudinal directions.

Appraisal of lacustrine aquifer’s groundwater potentiality and its hydrogeological modelling in southeastern Peshawar, Pakistan: implications for environmental geology, and geotechnical engineering

The Peshawar Basin is a part of the lower Himalayas that contains an enormous amount of groundwater storage. The evaluation of groundwater potential in the southern Peshawar district was done using well logging, lithostratigraphic properties, and combined hydrogeological and geophysical techniques. A total of 13 Vertical Electrical Sounding (VES) profiles were utilised to assess potential groundwater zones for surface resistivity studies. The aquifer system was delineated by comparing the data from five boreholes with the VES findings. An exploration of super-saturated groundwater potential was conducted, utilising parameters such as transmissivity (T), hydraulic conductivity (K), storativity, and the Dar Zarrouk analysis. The Dar Zarrouk analysis yielded average values of transverse resistance (TR), longitudinal conductance (S), and anisotropy (λ), which were determined to be 8069.12, 0.51, and 0.561, respectively. Similarly, average values of transmissivity (T), hydraulic conductivity (K), and storativity were obtained, resulting in 28.67, 0.24, and 0.000177, respectively. The saturated confined layer, characterized by highly saturated zones, was identified to begin at a depth of approximately 119 m and extend down to the lower boundary of the aquifer. The examined aquifer is composed of clay, sand, gravel, boulders, and loose layers of lacustrine mud that are interlayered to form an unconsolidated groundwater aquifer system. The aquifers in the region are highly developed and consisted of unconfined, semi-confined, and confined aquifer systems. As a result, it is possible to use the aquifer for groundwater development in the study area because of its low -to-medium discharge.

Origin of surface oxidation induced the nucleation and propagation of microcracks in TNM alloy

This study investigated the impact of surface degradation caused by oxygen (O) and nitrogen (N) elements in the environmental atmosphere on the service failure of nearly lamellar TNM alloy. The results show that oxidation-induced phase transformations at the surface and subsurface regions strongly affect the alloy's tensile properties at high temperatures. The precipitation of Al2O3, which disrupts the integrity of the Ti2AlN layer, has a weaker deformation resistance capacity compared to the Z-phase. Under stress conditions, numerous dislocations concentrate at the Al2O3 phase, causing Al2O3 particles to easily detach and initiating crack nucleation at the Z-phase/Al2O3 interface. This is the origin of oxidation failure. Cracks nucleate at the Al2O3 detachment region, propagate, and connect with surface microcracks induced by the rough and loose outer oxide layer structure. This leads to the rapid propagation of cracks into the subsurface. The consumption of β-stabilizing elements at the surface, along with the internal diffusion of O and N elements into the subsurface region, results in the formation of the hard brittle Z-phase at the subsurface lamellar structure and a transition from β0 to α2 at the lamellar colony boundaries. The precipitation of α2 and Z-phase also accelerates crack propagation. In summary, the failure mode shifts from toughness fracture to brittle fracture.

A Biodegradable Janus Sponge for Negative Pressure Wound Therapy.

Negative pressure wound therapy (NPWT) is effective in repairing serious skin injury. The dressing used in the NPWT is important for wound healing. In this paper, we develop biodegradable amphiphilic polyurethanes (PUs) and fabricate the PUs into sponges as wound dressings (Bi@e) with Janus pore architectures for NPWT. The Bi@e is adaptive to all the stages of the wound healing process. The Janus Bi@e sponge consists of two layers: the dense hydrophobic upper layer with small pores provides protection and support during negative pressure drainage, and the loose hydrophilic lower layer with large pores absorbs large amounts of wound exudate and maintains a moist environment. Additionally, antibacterial agent silver sulfadiazine (SSD) is loaded into the sponge against Escherichia coli and Staphylococcus aureus with a concentration of 0.50 wt%. The Janus sponge exhibits a super absorbent capacity of 19.53 times its own water weight and remarkable resistance to compression. In a rat skin defect model, the Janus Bi@e sponge not only prevents the conglutination between regenerative skin and dressing but also accelerates wound healing compared to commercially available NPWT dressing. The Janus Bi@e sponge is a promising dressing for the NPWT.

LEAP centrifuge tests on retaining walls at Cambridge University

Retaining walls and other waterfront structures were seen to suffer severe damage due to soil liquefaction in previous earthquakes. As part of the LEAP project, cantilever retaining walls with loose, saturated backfill were tested at various centrifuge centres participating in this endeavour. The toe of the retaining wall penetrated about 0.5 m into the dense sand layer underlying the loose sand layer. Retaining walls with different ratios of the retained height h over the penetration depth d were tested. As part of the LEAP project, additional testing was carried out at Cambridge to consider the effect of the wall size on its deformation following liquefaction. It will be shown that a larger wall will suffer more rotation and wall top displacement than a smaller wall with the same h/d ratio. This can have implications for numerical modelling in terms of how well the constitutive models capture the suppressed soil dilatancy at higher confining pressures.

Corrosion Behavior of the 2024 Aluminum Alloy in the Atmospheric Environment of the South China Sea Islands

The 2024 aluminum alloy, a structural material commonly used in aviation aircraft bodies, is susceptible to serious corrosion in marine atmospheric environments. This paper comprehensively studies the corrosion behavior of the 2024 aluminum alloy in the South China Sea atmosphere. Weighing, morphology observation, phase analysis, electrochemical testing, and other methods were used to study the corrosion law and corrosion mechanism of the 2024 aluminum alloy. The main conclusions are as follows: At the initial stage of exposure, pitting corrosion occurred on the surface of the 2024 aluminum alloy. After 3 months of exposure, the self-corrosion current density increased from 0.456 μA·cm−2 to 8.338 μA·cm−2. After 6 months of exposure, the corrosion developed into general corrosion. The main component of the corrosion product was Al2O3·3H2O. The product covered the surface to form a loose corrosion product layer, which had an inhibitory effect on corrosion. The self-corrosion current density was reduced to 2.359 μA·cm−2. After 12 months of exposure, the corrosion product layer fell off and became thinner, and the self-corrosion current density increased to 2.849 μA·cm−2. The corrosion kinetics conformed to the functional equation W = 0.00346t0.73891, indicating that the corrosion products have a certain protective effect on the matrix.

Systematic experiments and multiscale simulation calculations reveal chemical stability differences in dry/wet nanofiltration membranes

This study investigated the chemical stability differences between dry and wet nanofiltration membranes when immersed in strong acid and base environments. Systematic experimental studies were conducted on both types of nanofiltration (NF) membranes, supplemented by Molecular Dynamics (MD) simulations and Density Functional Theory (DFT) calculations. The results indicate that wet NF membranes, soaked in deionized water for a week, exhibit higher chemical stability compared to dry membranes treated only with air. Traditional air heating causes membrane pore contraction and excessive crosslinking. However, after a week of immersion in water, the polyamide (PA) layer gradually becomes a loose and well-extendable PA layer. MD simulations revealed that H+ and OH− ions possess lower diffusion coefficients and extended residence times in dry NF membranes, making them more prone to damage. Additionally, DFT calculations disclosed that the Gibbs free energy (ΔG) for amide bond hydrolysis in wet NF membranes, in the presence of water molecules, is elevated, significantly delaying their hydrolysis rate under extreme conditions. This study highlights the pivotal role of membrane wetness in the chemical durability of NF membranes and offers a novel perspective for improving membrane lifespan and efficiency.

Facile Preparation of Cellulose Beads with Tunable Graded Pores and High Mechanical Strength.

Cellulose-based hierarchical porous beads exhibit significant application potential in adsorption and separation systems due to their degradation and biocompatibility. However, the current fabrications of cellulose beads show poor mechanical properties and a difficult-to-regulate hierarchical porous structure, reducing their lifespan of use and limiting their application in fine separation. Here, we reported the facile creep-drop method to prepare cellulose beads that enabled systemic regulation of the macro-size, micropore structures, and mechanical properties by optimizing injection nozzle diameter, the composition of the coagulation bath, the temperature of the coagulation bath, and cellulose concentration. Notably, during the molding process, the H2SO4-Na2SO4 composite solidification bath endowed cellulose beads with a dense shell layer and a loose core layer, which achieved the integration of mechanical properties and high porosity. The cellulose beads exhibited high porosity (93.38-96.18%) and high sphericity (86.78-94.44%) by modulating the shell thickness of the cellulose beads. In particular, the cellulose beads exhibited excellent mechanical properties with a high compressive strength of 544.24 kPa at a 5% cellulose concentration. It is expected that these cellulose beads with tunable microstructures can realize their potential for applications in the fields of wastewater treatment, chemical engineering, bioengineering, medicine, and pharmaceuticals.

Effect of rust layer stabilization on dry and wet cyclic corrosion behavior of bridge weathering steel Q345qNH in simulated industrial atmospheric medium

Abstract It takes 3–5 years for the stable rust layer to form when the bridge weathering steel is used in the industrial atmosphere, and the loose rust layer appearing in the early stage will pollute the atmospheric environment. Therefore, a method for the rapid formation of stable rust layer is developed in this paper, and the influence of rust layer stabilizing treatment on corrosion behavior of bridge weathering steel Q345qNH in simulated industrial atmospheric medium is studied. The results showed that in simulated industrial atmospheric medium, the stabilizing treatment shortened the formation time of stable rust layer and significantly reduced the corrosion rate, which is 47.9 % lower than that of bare steel after 480 h of corrosion. During the whole corrosion process, the Iα-FeOOH/Iγ-FeOOH peak intensity ratio of the stabilizing treatment steel was always higher than that of the bare steel, and was 1.26 times that of the bare steel after 480 h corrosion. After the stabilizing treatment, the self-corrosion potential of the rust layer increases, the self-corrosion current density decreases, and the resistance of the rust layer after 480 h corrosion was 1.57 times that of the bare steel sample, and the protection of the rust layer was significantly improved.

Exploring the interlaminar toughening potential of carbon nanoparticles: Structural and size effects

This work explored the influence of the intrinsic structure and size of different carbon nanoparticles on the morphologies of their corresponding aggregated structures, as well as their interlaminar toughening effect in carbon fiber reinforced polymer composites. CNTs and Grs with different sizes were selected as building blocks of toughening layer, which were firstly well-dispersed into acetone and then spray-coated onto the surface of carbon fabrics. The results indicate that one-dimensional filamentous CNTs are prone to forming loose and porous layers, exhibiting better interlaminar toughening effects. On the contrary, the layers formed by two-dimensional sheet-like graphene are relatively dense at microscale, which weakens the interlaminar fracture toughness of the laminated plate. In addition, CNTs with short length have a larger BET surface area at nanoscale and form a porous layer at microscale, showing best interlaminar toughening efficiency.

Regenerated Graphite Electrodes with Reconstructed Solid Electrolyte Interface and Enclosed Active Lithium Toward >100% Initial Coulombic Efficiency.

Solid electrolyte interface (SEI) is arguably the most important concern in graphite anodes, which determines their achievable Coulombic efficiency (CE) and cycling stability. In spent graphite anodes, there are already-formed (yet loose and/or broken) SEIs and some residual active lithium, which, if can be inherited in the regenerated electrodes, are highly desired to compensate for the lithium loss due to SEI formation. However, current graphite regenerated approaches easily destroy the thin SEIs and residue active lithium, making their reuse impossible. Herein, this work reports a fast-heating strategy (e.g., 1900 K for ≈150ms) to upcycle degraded graphite via instantly converting the loose original SEI layer (≈100nm thick) to a compact and mostly inorganic one (≈10-30nm thick with a 26X higher Young's Modulus) and still retaining the activity of residual lithium. Thanks to the robust SEI and enclosed active lithium, the regenerated graphite exhibited 104.7% initial CE for half-cell and gifted the full cells with LiFePO4 significantly improved initial CE (98.8%versus 83.2%) and energy density (309.4versus 281.4Wh kg-1), as compared with commercial graphite. The as-proposed upcycling strategy turns the "waste" graphite into high-value prelithiated ones, along with significant economic and environmental benefits.

Effects of polyol and surfactant plasticisers on lyophilised rice starch wafers for buccal drug delivery

Rice starch is a promising biopolymer for buccal formulations but typical oven drying may promote starch retrogradation that affects mechanical properties. Hence, lyophilisation was proposed here to improve starch product's stability. This study aims to investigate the effects of plasticisers (sorbitol and Tween® 80, T80) on the characteristics and drug release profiles of lyophilised rice starch wafers incorporated with propranolol hydrochloride. The wafers were prepared by lyophilising starch mixture (5%w/v) with plasticiser (0.2 and 0.3 g/g) and drug (10, 20, 30%w/w). Control wafers exhibited loose layers with rough wrinkled surface. Sorbitol resulted in a dense structure with higher puncture strength (PS) but lower water absorption capacity (WAC) while T80 loosened the flakes that reduced PS and increased WAC. Drug inclusion decreased PS and increased WAC of unplasticised wafers. T80-plasticised wafers with drug had a lower PS and higher WAC than sorbitol-plasticised wafers. Particularly, T80-plasticised wafers achieved outstandingly high PS and the lowest WAC at 30%w/w drug. Drug dissolution of wafers relied mainly on the drug crystallinity and WAC at 10 and 30%w/w drug. Plasticisers reduced and increased drug dissolution at 10 and 20%w/w drug, respectively. This study highlights the potential of lyophilisation in preparing rice starch wafers for buccal delivery.

Understanding of the flocculating performance in varying salinity solutions of Chi-g-CPAM and CPAM

In this work, the adsorption performance of a novel chitosan-based flocculant (Chi-g-CPAM) and a cationic flocculant (CPAM) onto the kaolinite surface as well as the interaction mechanisms have been investigated by settling tests, atomic force microscopy (AFM) and quartz crystal microbalance with dissipation (QCM-D). When the KCl concentration of the solution altered from 1 mM to 100 mM, the settling rate of kaolinite suspension using CPAM deteriorated from 2.73 m/h to 1.97 m/h. However, the Chi-g-CPAM exhibited salt resistance as the settling rate changed slightly from 2.34 m/h to 2.44 m/h. From the QCM-D results, the Δf of CPAM onto silica sensor changed from − 3.6 Hz to − 33.6 Hz and -ΔD/Δf × 106 increased from 0.167 to 0.223, confirming that the CPAM layer adsorbed on the silica surface was thicker and more dissipative in 100 mM KCl solution. Meanwhile, the Δf of Chi-g-CPAM onto silica sensor changed from − 14.3 Hz to − 33.9 Hz. The conformation of Chi-g-CPAM layer changed slightly as the -ΔD/Δf × 106 increased from 0.174 to 0.186. From the AFM measurements in 1 mM and 100 mM KCl solution, the distance of adhesion forces between the silica probe and CPAM expanded from approximately 20 nm to around 50 nm, and the adhesion force changed from 1.9 nN± 0.1 nN to 21.3 nN± 0.1 nN. The interaction forces with a long range (∼100 nm) maintained at about 3 nN between the silica probe and Chi-g-CPAM. Such difference was mainly attributed to the steric hindrance effect originating from the shorter molecular chain of Chi-g-CPAM. In 100 mM KCl solution, the CPAM molecules with long chains had a more coiled conformation than Chi-g-CPAM, which resulted a train-like flat adsorption conformation and larger adhesion, and formed a loose and thick polymer layer of CPAM in high salinity. The insights into the flocculating performance in varying salinity solutions of CPAM and Chi-g-CPAM will contribute to the molecular design of chitosan-based flocculants for efficient wastewater treatment.

Seismic behavior of highway embankment reinforced with remedial countermeasures on saturated loose sandy layer

A hybrid pile system is proposed to suppress excessive settlement and lateral spreading, which are regarded as main causes of highway embankment failure due to earthquakes. This system, combining two groups of vertical and inclined piles arranged on both sides of highway embankment slope, can be applied to existing highway embankments. In this research, a series of 1 g shaking table tests were performed together with modeling the performance of highway embankments incorporating three cases with different reinforcements subjected to two sinusoidal waves. Several aspects of acceleration time history, pile deformation, and embankment settlement under three configurations were revealed and discussed to confirm the effectiveness of the proposed countermeasures. The results indicate that (1) the hybrid pile system can still ensure sufficient functionality to maintain the highway embankment after two consecutive strong earthquakes; (2) this system can also enhance the integrity of loose sandy layer to reduce the settlement and lateral spreading of embankment; (3) the inclined piles effectively reduce pile head deformation by increasing the shear strength of the pile.