Interfacial Area Research Articles

Improving reverse time migration of ground-penetrating radar under zero-time imaging conditions using cross-correlation superposition projection

ABSTRACT Aiming to address the issue of significant artefact interference in conventional reverse time migration (RTM) imaging under zero-time imaging conditions of ground-penetrating radar (GPR), this study proposes an improvement of RTM using cross-correlation superposition projection (CSP) to enhance imaging quality. The method is based on the original RTM imaging framework, where all single-trace signals are individually processed using RTM. The individual imaging results are then multiplied pairwise and added together to create a CSP. After normalizing the CSP and properly setting the adaptive threshold, the CSP can focus RTM imaging on the GPR signal reflection interface area, effectively removing artefact interference. Synthetic data test confirms that the CSP-improved RTM, when compared to conventional RTM and Laplace filtering methods, not only preserves all effective information in imaging but also eliminates artefact interference. This improvement significantly enhances the quality and resolution of the imaging results. Furthermore, the practicality and effectiveness of the CSP-improved RTM method in engineering applications have been validated using a set of measured GPR data.

Impact of Wettability on CO2 Dynamic Dissolution in Three-Dimensional Porous Media: Pore-Scale Simulation Using the Lattice Boltzmann Method.

Understanding the dissolution behavior of supercritical CO2 (scCO2) in porous media is crucial for efficient CO2 storage. However, the precise modeling of dynamic dissolution behavior at this pore scale remains a huge challenge, and the impact of wettability on this process still needs to be clarified. In this study, the influence of rock wettability on CO2 dynamic dissolution in the three-dimensional porous media is investigated using the lattice Boltzmann method (LBM). The LBM is coupled with scCO2-water two-phase flow, solute transport, and heterogeneous and homogeneous reactions. The size, number, and dissolution pattern of scCO2 bubbles during the dissolution process are observed under strongly water-wet, weakly water-wet, intermediate-wet, and mixed-wet conditions. The CO2(aq) concentration and pH are investigated, followed by a quantitative investigation of the impact of wettability on the specific interface area and the mass transfer coefficient. An empirical relationship between the specific interface area and scCO2 saturation is established. The findings reveal that under weakly water-wet and intermediate-wet conditions, the sizes of scCO2 clusters and monomers are small and mostly distributed at the dead end of the pores. In contrast, under strongly water-wet and mixed-wet conditions, the clusters are larger and interconnected, and distributed in the center of the pore. This results in a greater scCO2-water interface area, consequently enhancing the dissolution rate. Furthermore, a strong linear correlation is observed between scCO2 saturation and specific interface area. It is noted that as the hydrophilicity of the rock increases, the mass transfer coefficient initially rises and then declines.

Progress on the Sound Absorption of Viscoelastic Damping Porous Polymer Composites.

Porous polymer composites (PPC) have developed rapidly recently, which are widely used in various industrial fields. Viscoelastic damping is an important behavior of porous polymer composites, and it can determine the sound absorption for noise reduction applications. This review has mainly covered the viscoelastic damping and sound absorption of porous polymer composites. Different fabrication approaches of porous polymer composites are gathered. The mechanism of viscoelastic damping behavior is described, and also the sound absorption properties. Followed by the introduction of enhanced sound absorption of viscoelastic damping porous polymer composites, including the incorporation of fillers, microstructures modification, combination with nanofibrous materials, and multilayer configuration, etc. The incorporated fillers can effectively adjust the interfacial area in composites, and obtain desired bonding conditions. Microstructures modification is an effective tool to improve the morphologies of both polymer matrix and fillers, which can be achieved by chemical treatment and surface coating. The combination with lightweight nanofibrous layer can increase the low frequency absorption. The configuration of multilayer composites can improve both acoustical and mechanical properties for engineering applications. It is hoped that this comprehensive review is benefit for the promising development of porous polymer composites in related fields.

Using the total chemical potential to generalize the capillary pressure concept and therefrom derive a governing equation for two-phase flow in porous media

This work presents a governing equation (GE) for two-phase flow in porous media connecting capillary pressure to frictional pressure loss and external chemical potential supplied to a system in either stationary or diffusive equilibrium. It is based on the difference between non-wetting and wetting phase chemical potential (physically, pressure or energy density), which leads to a generalization of the capillary pressure concept. The difference in phase internal chemical potentials is characterized by changes in both interfacial areas and entropy densities due to variation in fluid saturations and is balanced by the system external chemical potential supplied. A definition of the capillary pressure concept is formulated based on the diffusive equilibrium criterion. The GE can explain the origin of the dynamic capillary pressure term, hysteresis, and connect the shift in the capillary pressure curve upon injecting water phases with varying salinities to all the other chemical potentials acting. It can connect, constrain, and potentially quantify all effects which can be formulated in terms of chemical potentials since it is based on a balance equation all two-phase flow systems must obey when either in stationary or diffusive equilibrium.

Titania stabilized Pickering emulsion for photocatalytic degradation of o-xylene

Efficient removal of insoluble volatile organic compounds (VOCs) from wastewater is a significant environmental challenge. In this work, we exploit the synergistic effect of photocatalysis and the high interfacial area of TiO2-stabilized Pickering emulsion to achieve efficient degradation of o-xylene, typically present in wastewater discharged from many industries. Interfacial photocatalysis is carried out by considering o-xylene in water Pickering emulsions stabilized by commercial titania nanoparticles in a multitube non-stirred reactor setup. Stable emulsions used for catalysis are formulated by optimizing o-xylene volume fraction, TiO2 concentration, pH, and homogenization conditions. The influence of photocatalyst loading, emulsion droplet size, and reaction conditions are systematically examined to determine their influence on the rate of photocatalytic degradation of o-xylene. Due to enhanced photocatalytic activity compared with conventional stirred batch photocatalysis, the TiO2-stabilized Pickering emulsion is found to increase the degradation rate and removal efficiency of o-xylene significantly. Furthermore, the Pickering emulsion stability during the photocatalytic process is studied, demonstrating the capacity of the emulsions to maintain stability and catalytic activity over a longer time period. The distinctive characteristics of Pickering emulsions – excellent storage stability and enhanced photocatalytic activity – make them a promising option for advanced wastewater treatment. The findings lead to the development of ecologically acceptable and sustainable VOC degrading strategies, which might be used in industrial and home wastewater treatment systems.

ZnO modified carbon fiber-matrix interfacial evaluation via nanoscale digital image correlation and nanoindentation

Improving the adherence of the fiber-matrix interface is an important step for enhancing the capabilities of polymer composites. In this study, carbon fibers were modified by growing zinc oxide (ZnO) nanorods on the fiber surface using a hydrothermal approach, with the aim of increasing the interfacial area and enhancing the friction between the fiber and the matrix. To fully understand the deformation mechanisms at the interface, a microscale evaluation combining nanoindentation with digital image correlation (DIC) for mapping the deformations by using nanoscale speckles is developed in this work. The main objective of this research was to develop a protocol for speckling the modified single fiber composite and show that DIC can be used in microscopic level and to evaluate the fiber-matrix interface by means of nano indentation. The speckle pattern was created using Ti nano powder and used to generate the strain maps in the fiber-matrix interface region. A comparative analysis of DIC results from ZnO modified carbon fibers has shown that shear strains around the interfacial boundary are 60 % reduced on average, as compared to neat carbon fibers, across all nano indentations from 8mN to 65mN of peak load. Results used direct strain measurements to confirm that modification by ZnO growth on the surface of individual fibers has a significant benefit to the interfacial mechanical properties of fiber-matrix composites.

Elucidating flow-directed 98% CO2 absorption using millimeter-sized coiled flow inverters: Nanocellulose-aided sustainable scope

The Sustainable Development Goals (SDGs) adopted by the United Nations drive the global efforts to discover a sustainable carbon capture method for the reduction of anthropogenic CO2 emissions. Concentrated alkanolamine solutions are being used as CO2 capture mediums for batch processes amid several disadvantages, such as energy intensiveness and poor efficiency. In this work, millimeter-sized coiled flow inverters (CFI) have been explored as a point-source CO2 capture tool for highly efficient, continuous operations. Solvent and CO2 gas flow rates are found to dictate the slug flow regime and, more specfically, slug lengths. High interfacial area and residence time remain the driving factors for enhanced CO2 capture using CFI. About 98% CO2 absorption efficiency has been achieved for 3% aqueous diethanolamine solution in CFI . The efficacy of nanocellulose, a sustainable nanomaterial has been unearthed for CO2 capture at low flow rate.

Interface of Human Resource Accounting with Accounting and Finance and Performance Evaluation

The purpose of this study is to report a link between the three disciplines of human resource accounting, accounting and finance and performance evaluation through a conceptual framework highlighting the interfaces between them. The term interface here refers to the points of interaction, connection or overlap between these three disciplines, highlighting how these disciplines interact, intersect or work together within the conceptual framework. The conceptual framework is designed based on a previous literature review. The final outcome of this study is a conceptual framework which reports the interface areas between human resource accounting and accounting and finance and between human resource accounting and performance evaluation, along with the individual roles of accounting and finance, human resource accounting, and performance evaluation disciplines in the interface development. This study contributes to the existing body of accounting literature by showing how accounting and finance lays down the foundation for the valuation and reporting of human resources in an organization, which in turn, facilitates in performance evaluation.

Characterization of the oil water two phase flow in a novel microchannel contactor equipped with helical wire static mixer

This study investigates an oil/water two-phase system to assess the potential efficacy of a novel passive mixer in enhancing the liquid-liquid interfacial area within a micro-channel contactor. In this system, two fluids are introduced into a microchannel with a diameter of 800 μm and a length of 20 cm, which is equipped with a stainless-steel helical wire measuring 250 μm in diameter. Throughout the experiments, both fluids are supplied at equal flow rates, and the dominant forces, including attachment and detachment forces, are examined. The results reveal a critical Weber number of 3.8 × 10−³, at which the first detachment occurs. A comparison between microchannels with and without the passive micromixer demonstrates that greater slug breakup occurs in the system incorporating the helical wire micromixer. This innovative configuration results in a significant reduction in slug/droplet size compared to a microchannel without a barrier, decreasing from approximately 600 μm to 390 μm at a flow rate of 0.8 mL/min. Additionally, a flow map is presented, illustrating three distinct flow regimes: flow contains long slug, Slug-droplet flow, and droplet flow regimes, with the droplet flow regime covering the largest area. The findings indicate that the implementation of this innovative passive mixer substantially increases the interfacial area, providing significant advantages for mass transfer applications.

Nanoheteroepitaxy of Ge and SiGe on Si: role of composition and capping on quantum dot photoluminescence.

We investigate the nanoheteroepitaxy of SiGe and Ge quantum dots (QDs) grown on nanotips substrates realized in Si(001) wafers. Due to the lattice strain compliance, enabled by the nanometric size of the tip and the limited dot/substrate interface area, which helps to reduce dot/substrate interdiffusion, the strain and SiGe composition in the QDs could be decoupled. This demonstrates a key advantage of the nanoheteroepitaxy over the Stranski-Krastanow growth mechanism. Nearly semi-spherical, defect-free, ∼100 nm wide SiGe QDs with different Ge contents were successfully grown on the nanotips with high selectivity and size uniformity. On the dots, thin dielectric capping layers were deposited, improving the optical properties by the passivation of surface states. Intense photoluminescence was measured from all samples investigated with emission energy, intensity, and spectral linewidth dependent on the SiGe composition of the QDs and the different capping layers. Radiative recombination occurs in the QDs, and its energy matches the results of band-structure calculations that consider strain compliance between the QD and the tip. The nanotips arrangement and the selective growth of QDs allow to studying the PL emission from only 3-4 QDs, demonstrating a bright emission and the possibility of selective addressing. These findings will support the design of optoelectronic devices based on CMOS-compatible emitters.

Methanogenic activity in water-saturated reservoir analogues for underground hydrogen storage: The role of surface area

The activity of methanogenic Archaea in porous formations is influenced by various pore characteristics, including porosity, surface area, and the gas-liquid interfacial area. This study explores the impact of surface area on methanogenic activity using techniques such as MICP, NMR, SEM, and μCT. The cells of Methanothermococcus thermolithotrophicus, ranging from 1 to 2 μm, indicate that pores smaller than this threshold are not accessible for microbial traversal and colonization. Upon normalization of microbial activities based on pore volume and interfacial area, the findings exhibit strong correlations with specific surface areas of accessible pores in the examined rocks, as determined by MICP, NMR, and SEM. These areas ranged from 0.001 to 0.017 m2/g, 0.003–0.024 m2/g, and 0.012–0.02 m2/g, respectively. The normalized activities increase from 0.19 to 0.44 mM/(h·cm3·cm2) with an increase in the specific surface area, varying by method. Furthermore, an empirical model has been established to quantitatively evaluate hydrogen loss during underground hydrogen storage or the efficiency of bio-methanation, incorporating pore volume, specific surface area, and interfacial area.

Flower-like NiFe layered double hydroxide/Bi2WO6 S-scheme heterojunction for photodegradation of ciprofloxacin under visible light

Photocatalytic degradation stands as an effective remedy to solve the global environmental pollution caused by organic pollutants. In this study, we synthesized a NiFe layered double hydroxide/Bi2WO6 (NF-LDH/BWO) Step-scheme (S-scheme) heterojunction. The attachment of NF-LDH particles on flower-like BWO increased the active sites and the interface area between two pure materials. The construction of LDH/BWO heterojunction endowed with improved light absorption capacity and boosted separation efficiency of photo-generated carriers. Consequently, compared with BWO and NF-LDH, the NF-LDH/BWO composites showed enhanced photoactivities. At NF-LDH mass ratio of 10%, the optimal degradation rate of ciprofloxacin (75.9%) within 60 min under visible illumination was achieved, 1.43- and 9.37-fold those of BWO and NF-LDH, respectively. In addition, the NF-LDH/BWO composite also demonstrated excellent cyclic stability. The S-scheme mechanism was proposed based on both experimental and density functional calculation results.

Insights into Thermal Conductivity at the MOF-Polymer Interface.

Understanding the thermal conductivity in metal-organic framework (MOF)-polymer composites is crucial for optimizing their performance in applications involving heat transfer. In this work, several UiO66-polymer composites (where the polymer is either PEG, PVDF, PS, PIM-1, PP, or PMMA) are examined using molecular simulations. Our contribution highlights the interface's impact on thermal conductivity, observing an overall increasing trend attributable to the synergistic effect of MOF enhancing polymer thermal conductivity. Flexible polymers such as PEG and PVDF exhibit increased compatibility with the MOF, facilitating their integration with the MOF lattice. However, this integration leads to a moderated enhancement in thermal conductivity compared to polymers that remain separate from the MOF structure, such as PS or PP. This effect can be attributed to alterations in phonon transport pathways and shifts in interfacial interactions between the polymer and MOF. Specifically, the infiltration of the polymer like PEG and PVDF into the MOF disrupted the MOF's ordered network, introducing defects or barriers that hindered phonon propagation. In contrast, nonpolar and rigid polymers like PP, PMMA, PS, and PIM-1 exhibited greater improvements in thermal conductivity when combined with MOFs compared to the flexible polymers PVDF and PEG. Most notably, our analysis identifies a critical interface region within approximately 30-50 Å that profoundly influences thermal conductivity. The interface region, as indicated by the density profile and radius of gyration, is notably shorter but plays a pivotal role in modulating the thermal properties. The sensitivity of the system to these interface characteristics underscores the crucial role of this particular interface area in dictating the thermal conductivity. Our findings emphasize the sensitivity of thermal conductivity in polymer matrices to interface characteristics and highlight the critical role of a specific interface region in modulating thermal properties.

Covalently Linked 2D-Co3O4/GO Heterostructures: Catalytic and Electrochemical Properties.

Covalently cross-linked 2D heterostructures may represent a ground-breaking approach to creating materials with multifunctionalities. To date, however, this field still remains relatively unexplored. In the present work, Co3O4/GO covalently linked heterostructures (Co3O4/GO-CL) were produced using 2D-Co3O4 functionalized with (3-aminopropyl)triethoxysilane (APTES) to react with the carboxyl groups of graphene oxide (GO). The surface and interface properties of the final material were assessed through electrochemical and catalytic studies. We found that the covalent bonds lead to a self-standing and ordered final structure, not observed for the noncovalent material (Co3O4/GO-nCL), also produced for comparison. The catalytic activity of Co3O4/GO-CL over the degradation of Rhodamine 6G showed great performance and the possibility of recycling the catalyst. Electrochemical evaluation stated higher specific capacitance for the covalently bonded material (468 F g-1 against 110 F g-1). Overall, results showed that the covalent bonds may be improving charge-transfer and interfacial area features, thus leading to enhanced catalytic and electrochemical performances.

Two-group interfacial area concentration model for dispersed gas-liquid flows in large-diameter pipes

Interfacial area concentration (IAC) plays a critical role in heat and mass transfers between gas and liquid phases through the interfaces. As interfacial area increases, mass and heat transfers between phases increase. Hence, a reliable IAC estimation is important for two-phase flow numerical simulations to conduct engineering designs and safety analyses. Gas bubbles show different behavior according to their shapes and sizes. Based on the size, gas bubbles can be classified into two groups that show different characteristics, such as IAC. Hence, two-group modeling helps to achieve a general approach for estimating the IAC in bubbly to beyond-bubbly flow regimes. Available models in the literature use empirical correlations to obtain group one and group two void fractions. These empirical approaches are not reliable for different flow conditions. In addition, these models are usually complex with several empirical constants. This study aims to develop a two-group area-averaged IAC model for upward vertical dispersed flows through large-diameter pipes. In addition, this study proposes using a general approach based on the two-group drift-flux model to calculate two-group void fractions rather than applying empirical correlations. The models are evaluated using 156 two-group measured data points in dispersed flow conditions through large-diameter pipes. The resulting prediction errors for group one and group two IAC models are 24.1 % and 34.2 %, and the errors for group one and group two void fraction predictions are 22.8 % and 25.6 %, respectively.

Cu-bearing HHCCI interface combined with first principles calculation and corrosive wear resistance

The corrosive wear resistance of copper-bearing HHCCI was tested through experiments and HRTEM, combined with first-principles calculations to study the atomic structure, interface fracture work, thermodynamic stability, electronic structure and bonding structure of six Fe3Cr4C3(01 1‾ 0)/γ-Fe(101) interface models with different termination methods. The HRTEM results show that the interface formed by (01 1‾ 0) of M7C3-type carbide and (101) of the austenite matrix is a coherent interface. The first principles calculation results show that the interface formed by the Fe3Cr4C3(01 1‾ 0)-Cr termination model and the γ-Fe (101)-2 termination model has the highest interface bonding strength. The Fe-end/7Fe-2 interface model is the most stable. Both the interfacial chemical energy and the interfacial elastic energy will affect the overall thermodynamic stability of the Fe3Cr4C3(01 1‾ 0)/γ-Fe (101) interface. The fracture work of Fe3Cr4C3(01 1‾ 0) and γ-Fe (101) is greater than the corresponding interface adhesion work. Moreover, the fracture work on each terminal end of M7C3 along the (01 1‾ 0) surface is higher than that on each terminal end of γ-Fe along the (101) surface. The failure of HHCCI during corrosive wear may mainly occur in the interface area or the side close to the γ-Fe matrix. The chemical bonds in the Fe-end/7Fe interface are mainly Fe-Fe metal bonds, Fe-Cr metal bonds and some Fe-C polar covalent bonds. The chemical bonds in the Cr-end/7Fe interface are mainly Cr-Fe metal bonds and some Cr-C polar covalent bonds. The chemical bonds in the C-end/7Fe interface are mainly composed of Cr-Fe metal bonds, C-Fe polar covalent bonds and part of C-Cr polar covalent bonds, as a result, each interface exhibits different corrosive wear resistance potentials.

Effect of size and loading of waste single-used plastic (SUP) aggregates on a bio-based high density polyurethane composite

Abstract The utilization of waste single-use plastic (SUP) as fillers by containment in a polyurethane matrix was investigated as an alternative solution to the detrimental disposal of these waste materials. High-density bio-based rigid polyurethane composites were prepared by adding polyol, isocyanate, and additives, along with densified SUP, which served as aggregate fillers to enhance the bulk density and flexural strength of rigid polyurethane while increasing the thermal conductivity. The aggregated SUPs were prepared using agglomeration-densification machine and exhibited size variations of 12.44 mm (A), 14.12 mm (B), and 15.56 mm (C). The resulting aggregates were added to the rigid polyurethane matrix at varied loadings of 40%, 50%, and 60% v/v. The green composites were cured in heated hydraulic press at constant temperature and pressure. Based on the obtained results, it was found that the formulation with a SUP size of C and a loading of 60% produced the composite of highest bulk density due to relatively high density of agglomerated SUP as the size enlarges. Additionally, the SUP size of A and a loading of 50% (50A) exhibited the highest flexural strength value. This behaviour was attributed to the increased filler-matrix interfacial area achieved with the smallest size aggregates. However, a further increase in aggregate loading resulted in a decrease in this property as common attribute for composite materials. On the other hand, it was revealed that increasing the loading of SUP aggregates provided a lesser insulating effect due to the increase in thermal conductivity resulting from the presence of filled pores within the polyurethane foam. The findings of this study contributed to understanding the effects of aggregate size and loading on the mechanical and thermal properties of the composite material, providing valuable insights for the development of energy-efficient and environmentally-friendly polyurethane structures.

A novel approach to improving the interfacial strength of 3D printed Al–GNP composites by modifying GNP with MgO

In this study, the MgO-coated graphene nanoplatelets (GNP)-reinforced aluminum matrix AlSi10Mg composites are fabricated by mechanical alloying and a 3D printing process. The interfacial structure of GNPs–Al has been investigated using high-resolution transmission electron microscopy, and their strengthening mechanism has been analyzed. A weak amorphous Al2O3 was found at the GNP–Al interface area in the composites made with uncoated GNPs. The structure of amorphous Al2O3 becomes distorted when load transfer is initiated, causing the detachment of GNPs from the matrix. This results in quick failure at the interface between uncoated GNPs and aluminum, restricting its overall strength. Once GNPs are coated with MgO, an Al/C mixing zone forms at the contact area, resulting in increased interface strength. The MgO coating on the GNP serves as a protective barrier, preventing the creation of a weaker amorphous Al2O3 layer at the interface and facilitating direct interaction between the GNP and Al matrix. The stress–strain curve demonstrates a 27.5% enhancement in tensile strength in the MgO-coated GNP–Al composite compared to the composite with uncoated GNPs. The strength is increased while maintaining toughness through load transmission of GNPs, bridging, and enhancing dislocation storage capacity by the Mg-rich phase. This study offers a new reference for strengthening 3D-printed aluminum alloys using GNPs.

RANCANG BANGUN UI/UX APLIKASI E-COMMERCE BERBASIS FRAMEWORK CODEIGNITER MENGGUNAKAN MODEL LEAN USER EXPERIENCE

In today's era, some people require more specialized marketplaces for selling items such as driving equipment or automotive-related products. Individuals need consignment services to sell their driving gear like helmets, driving jackets, and other related items. Many people face difficulties in finding suitable and secure storage spaces for their belongings. This study explores the rapid expansion of internet usage, which has spurred the emergence of new business models, notably online marketplaces for buying and selling goods. The research focuses on developing a simple yet effective online store platform, particularly tailored for sellers at the Indonesian Helmet Shop. Employing the prototype method, this research constructs the application through various modeling techniques including use case diagrams, class diagrams, activity diagrams, and sequence diagrams. The primary objective is to create a lightweight, web-based marketplace application that enhances the transaction process between consignment providers and consumers. Preliminary findings suggest that the application facilitates efficient user interactions and transactions. However, further development is required in the areas of user interface (UI) and user experience (UX) to ensure greater consumer satisfaction and engagement. This study underscores the potential of tailored digital solutions in optimizing e-commerce platforms, particularly in specialized market sectors.

Fabrication and characterization of novel curcumin-loaded thermoreversible high amylose maize starch emulsion gel

This study developed a novel thermoreversible emulsion gel system based on high amylose maize starch (HAMS) and investigated the impact of the oil-to-water ratio on its physicochemical properties and encapsulation performance (using curcumin as model guest molecule). Electron microscopy showed a tightly porous network structure of the HAMS-based emulsion gels. Thermal results revealed a sol-gel transition occurring in the range of 59.41 to 67.64 °C for the prepared emulsion gels. Rheological analysis suggested that all samples displayed shear-thinning behavior and HAMS-based emulsion gels exhibited typical gel-like behavior with the gel strength bolstered by higher aqueous phases. Particle size analysis showed that droplet size of emulsion gel decreased from 245 to 184 nm with increased starch aqueous phase content. Texture profile analysis indicated enhanced strength, hardness, and chewiness of the emulsion gel with increased aqueous phases. Curcumin encapsulation efficiency in the HAMS-based emulsion gel also improved with higher aqueous phase content, reaching up to 93.82 %, which attributed to the smaller droplets caused increased interfacial area. The novel HAMS-based emulsion gel system showed considerable encapsulation capacity and desirable mechanical properties. It provided valuable insights into the application of starch-based emulsion gels in food and medical area.