Water Solution Research Articles

Ionic Bent-Core Pillar[n]arenes: From Liquid Crystals to Nanoaggregates and Functional Applications.

Herein, we report the first examples of supramolecular systems from bent-core-based pillar[n]arenes through ionic bonds. These ionic materials have been prepared by the interaction of an amino-ended pillar[5]arene (P5N10) and three different carboxylic acids, including bent-core moieties. The bent-core units are based on ester, biphenyl, and azobenzene structures bearing two different flexible spacers between the carboxyl group and the central bent-core aromatic units. The ionic pairs segregate the molecular blocks, leading to columnar liquid crystal organizations. These ionic supramolecular compounds exhibit interesting results as proton-conductive materials. Furthermore, the introduction of azobenzene units in the bent-core structure has provided a photoresponse to the proton conduction materials. Interestingly, the amphiphilic character generated by the ionic pairs and the hydrophobic bent-core structures allows their molecular self-assembly in water solution, resulting in aggregates of appealing morphologies. The structural modifications of the bent-core units (i.e., connecting bonds at the lateral structure and spacer lengths) provide an attractive analysis on the relationship between the chemical structure and the morphology of the aggregates (fibers, chiral ribbons, nanotubes...). Additionally, the self-assembly process and evolution of the aggregates from fibers to nanotubes have been studied with several techniques.

Promoting the circularity of ceramic materials through cold sintering of aggregates from construction and demolition waste

A ceramic composition containing 95 wt% of construction and demolition waste-like material was consolidated by cold sintering process at 200 °C using KOH water solutions as the liquid medium. The relative density of the samples reaches ∼90 % of the theoretical one for process conditions of 600 MPa and 60 min. A post-annealing process at 1100 °C of the as-cold sintered samples causes a slight increase in the relative density and of their mechanical strength compared with conventionally sintered samples at 1100 °C and increases the shape factor of the Weibull distribution, thus increasing the reliability of the component. It is shown that cold sintering of the material avoids its high pyroplasticity, providing low shrinkage and reducing internal defects in the ceramic. This work represents the first exploration of the viability of manufacturing ceramic tiles with high recycled content contributing to the transition to a greener world.

Semi-implicit schemes for modeling water flow and solute transport in unsaturated soils

The coupled model of water flow and solute transport in unsaturated soils is addressed in this study. Building upon previous research findings by Keita, Beljadid, and Bourgault, we investigate a class of second-order time-stepping techniques where two free parameters are introduced, to identify the most stable and accurate scheme. The spatial discretization of the Richards equation is accomplished using the mixed finite element method. The proposed approach involves formulating noniterative schemes using an extrapolation formula and Taylor approximation in time to linearize nonlinear terms. Additionally, a specialized regularization technique is applied to ensure the convergence of the proposed numerical methods. Numerical simulations are conducted to determine the optimal scheme for solving the Richards equation, which is subsequently extended to the transport equation.Numerical simulations of water flow reveal the good accuracy of three schemes—SBDF, MSBDF, and Richards-M2 for homogeneous and heterogeneous soils. Notably, the SBDF scheme stands out for its computational efficiency and stability, especially when gravity forces dominate over capillary forces. Through numerical analysis of the coupled semi-implicit schemes, our results affirm the SBDF scheme’s superior robustness, establishing it as the optimal choice among the proposed numerical methods. Therefore, the SBDF scheme is employed to solve the coupled model of water flow and solute transport. We conducted various numerical experiments to solve the coupled model, addressing scenarios including single and multispecies nitrogen transport, pore water electrical conductivity, and nitrate transport. The SBDF scheme’s accuracy was rigorously verified through comparisons with reference solutions and experimental data. This establishes the SBDF scheme as an efficient alternative to traditional implicit methods for modeling water flow and solute transport in unsaturated soils.

Effect of nonpolar solute on the local structure of aqueous solution: Orientation-dependent integral equation study of nonpolar solute in rose water model

The presence of solute in water, even in small quantities, changes the properties of water. The ability of water molecules to form hydrogen-bonds is decisive for the structural and thermodynamic properties. When the solute is added to water, the network of hydrogen bonds is disrupted, changing the structure and properties of the water. In this work, we have used a simple two-dimensional rose water model together with orientation-dependent integral equation theory (ODIET) to gain insight into the effects of nonpolar solutes on the local structure of aqueous solutions. The theory shows good agreement with the radial distribution functions and enthalpies of solvation obtained with simulations, while improving the results of the orientation-averaged version of the theory. The advantage of the two-dimensional water model together with ODIET is that angle-dependent properties can be calculated relatively quickly and easily visualised. Using the potential of the mean force derivatives, the effect of added nonpolar solute on the local structure of the solution was investigated. Depending on the size of the solute, two different regimes of the effect of the solute on the structure of the solution were identified. Small solutes increase the tendency of water to form hydrogen-bonds and at the same time decrease solvation and association of the solute. On the other hand, large solutes have the opposite effect - they decrease the HB tendency of water and increase solvation and association of the solute.

Adsorption of silver ions onto chitosan hydrogel: Structural studies

Chitosan indicate a significant potential in the field of water treatment due to polymer high porosity, large specific surface area and its ability to bind strongly heavy metal ions form aqueous solutions. Therefore, chitosan based hydrogels have been fabricated by physical crosslinking of the polymer chains via sol–gel method using sodium β-glycerophosphate (β-GP) for silver ions (Ag) removal from water solutions. The aim of this study was to provide experimental studies under batch conditions to perform adsorption isotherm and evaluate the effect of silver adsorption onto chitosan hydrogel morphological and structural changes using SEM, XRD, FTIR and EDX analyses. Obtained results provides the data on the structural changes in the chitosan hydrogels under Ag adsorption process. The FTIR spectra confirmed that the C-NH2 and OH groups contribute to the formation of chitosan - silver ion complexes. The presence of adsorbed Ag in the samples < 0.8 gAgL−1 were evidenced by the characteristic peak at 2θ = 46.35°. Regarding to EDX analysis the adsorption efficiency toward Ag ions, rises with an increase in Ag initial concentration, resulting in L-type isotherm. The percentage removal of silver ions efficiency obtained 34 % for the highest Ag initial concentration (10 gAg L−1). SEM micrographs after Ag adsorption performed morphology as homogeneous porous network and reveals Ag present in the structure resulting from effective Ag adsorption. This study verified structural changes resulted from silver ions adsorption and confirmed the potential for thermosensitive chitosan hydrogels to applied as an adsorbent for water treatment applications.

Design of a Phantom Mimicking Rectal Lymph Nodes for Magnetomotive Ultrasound

ObjectiveDurable and stable phantoms for verifying and validating the new magnetomotive ultrasound technique are lacking. Here we propose a phantom design to address this need. MethodsA mixture of styrene-butylene/ethylene-styrene (SEBS) in mineral oil and glass beads as a scattering material acted as a bulk material, in which a polyvinyl alcohol (PVA) inclusion containing magnetic nanoparticles in water solution and graphite was embedded. The design mimics nanoparticle-laden lymph nodes embedded in mesorectal fat, as would be the clinical scenario for diagnostic support of staging rectal cancer using magnetomotive ultrasound. ResultsThe estimated reflection between the insert and bulk material was 10%, matching the clinical case of a lymph node within fat (9%). Speed of sound, attenuation, and Young's modulus of the bulk material were matched with those of body fat. The insert also matched the acoustic and elastic properties of lymph node tissue except for attenuation, which was lower than that given in the literature. Glass beads and graphite were used to control backscatter levels in the respective tissue mimics, providing a contrast of -3.8 dB that was consistent with clinical image appearance. The magnitude of magnetomotion remained stable in three separate samples over the course of 3 weeks. ConclusionWe have developed a phantom for magnetomotive ultrasound that combines the stability of an oil-based bulk material with the necessity of using a water-based material for the insert. The production procedure may be applied to other phantoms where one tissue type needs to be embedded within another.

Formation of zinc tetraammine difluoride and dinitrate and conversion to zinc oxide and zinc hydroxyfluoride under ambient conditions

The zinc tetraammine complexes [Zn(NH3]4]F2 (ZAF) and [Zn(NH3]4](NO3)2 (ZAN) have been isolated from methanolic ammonia and characterized by single crystal X-ray diffraction and Raman spectroscopy. As determined from Raman data, the tetrahedral structure of the zinc tetraammine cation complex is sustained in solutions that contain high concentrations of ammonia. Dilution of ZAF or ZAN solutions in bulk water results in the deposition of ZnO as determined by X-ray powder diffraction (XRD). Lower dilution, as when aqueous ZAF is applied to wet surfaces, results in Zn(OH)F deposition as identified by XRD. These mineral products are readily obtained from zinc tetraammine solutions under ambient conditions and lend themselves to biomedical and materials applications.

Polysaccharide fractions extracted from Lactarius quieticolor mushroom exhibit immune stimulatory activities on macrophages

Several beneficial properties have already been observed for mushrooms extracts containing polysaccharides, one of the main components present in these fungi. In order to obtain these extracts and clarify their composition, different extraction and characterization methods can be applied, contributing to understanding its biological effects. In this research, we evaluated three different crude fractions obtained through cold water, hot water, and alkaline solution, from the mushroom Lactarius quieticolor. Each sample was totally characterized by NMR (1H, 13C, HSQC-DEPT), GC–MS (monosaccharide composition and methylation analysis) and HPSEC (homogeneity and relative Mw). The results showed a mixture of different polysaccharides, including D-galactans and D-glucans in each fraction. All the extracts presented immunostimulant activity in murine RAW 264.7 macrophages, stimulating NO secretion and inducing morphological alterations that were typical of activated cells. These effects were more intense for alkaline fraction (EA), which have higher amounts of mannose and 3,6-di-O-substituted-Glcp units. The results obtained show that crude fractions can potentially stimulate immune cells, which indicates that the consumption of this edible mushroom can bring great benefits to health, being considered an excellent food due to its good biological properties.

Effect of different parameters on mode I fracture toughness of resin samples manufactured by DLP

Abstract Additive manufacturing is spreading rapidly in almost all industries, from household to advanced engineering. Components produced by Digital Light Processing (DLP) are not comprehensively characterized, but exceed the capabilities of many AM processes. Its advantages include the ability to produce highly complex designs, superior precision, fast printing and lower operating costs. The present paper investigates the mode I fracture toughness (KIC) of UV-sensitive resin specimens obtained through DLP process. Single edge notch bending (SENB) specimen were 3D printed and tested according to the ASTM D5045 standard. The influence of printing orientation-PO (0°, 45° and 90°), resin color-RC (white, black and transparent) and corrosive environment-CE (air, water and saline solution) was studied. It was observed that all the studied parameters have some effect on the fracture properties. The highest KIC values were obtained for 45°-PO, white-RC (1.88 MPa•m0.5) and saline solution-CE (2.24 MPa•m0.5). However, the greatest influence is highlighted by RC (∼92%), while CE (∼32%) shows a minimal effect. The fracture surface of the investigated samples is influenced by the printing parameters.

Examining the Mid to Long‐Term Variability in Saturated Hydraulic Conductivity of Sandy Soils and Its Influencing Factors Under Constant Head Test in the Laboratory

AbstractSaturated hydraulic conductivity (Ks) is a crucial parameter that influences water flow in saturated soils, with applications in various fields such as surface water runoff, soil erosion, drainage, and solute transport. However, accurate determination of Ks is challenging due to temporal and spatial uncertainties. This study addresses the knowledge gap regarding the long‐term behavior of Ks in sandy soils with less than 10% fine particles. The research investigates the changes in Ks over a long period of constant head tests and examines the factors influencing its variation. Two sandy samples were tested using a hydraulic conductivity cell, and the hydraulic head and discharge were recorded for over 50 days. The results show a general decline in Ks throughout the test, except for brief periods of increase. At the end of both tests, there are noticeable reductions in the saturated hydraulic conductivities of the samples, with one sample being 96% and the other sample 91% less than the maximum recorded saturated hydraulic conductivity during the tests. Furthermore, the relationship between flow rate and hydraulic head gradient does not follow the expected linear correlation from Darcy's law, highlighting the complex nature of sandy soil saturated hydraulic conductivity. The investigation of soil properties in three different sections of the samples before and after the tests revealed a decrease in the percentage of fine particles and a shift in specific gravity from the bottom to the top of the sample, suggesting particle migration along the flow direction. Factors such as clogging by fine particles and pore pressure variation contribute to the changes in Ks. The findings of this research show the importance of considering changes of saturated hydraulic conductivity during constant‐head laboratory tests. Therefore, this study provides evidence for the requirement to further assess the laboratory methods for measurement of the saturated hydraulic conductivity in sandy soil mixtures.

Investigating intermittent immersion during osmotic dehydration of mango (Mangifera indica L. Moench). Part B mathematical modeling of D2I and D3I kinetics in mango (Mangifera indica L. Moench) slices

This work aims to investigate the dynamics of water loss (WL) and solute gain (SG) during dehydration impregnation by immersion (D2I) and intermittent immersion (D3I). WL and SG of mango slices, 4 × 1× 1 cm3 in size, during dehydration immersion impregnation (D2I) and dehydration impregnation by intermittent immersion (D3I) were determined at 35, 45 and 55 °C for 270 min. Mango slices were immersed in a hypertonic sucrose solution of (61.6 ± 0.2) °Brix at a ratio of 6 mL of hypertonic solution per gram of fruit. Five semi-empirical models, two of which have been modified, were used to study mass transfer during D2I and D3I, namely the Azura, Weibull, Crank, Modified Crank I, and Modified Crank II models. The equilibrium water loss (WL∞), the equilibrium solute gain (SG∞), the diffusion coefficient, and activation energy were determined using the Modified Crank II model which was the best of all the tested models. Equilibrium water loss during D2I decreased with increasing temperature, while during D3I it increased with temperature. The SG∞ during D2I and D3I increases with temperature but was higher in D2I than in D3I. The average water diffusion coefficients were (6.02 ± 2.62) × 10−8 m2 s−1 for D2I and (4.89 ± 0.55) × 10−8 m2 s−1 for D3I and the average solute diffusion coefficients were (4.45 ± 0.53) × 10−8 m2 s−1 for D2I and (8.33 ± 0.79) × 10−8 m2 s−1 for D3I. The activation energies for WL in D2I and D3I were respectively 38789 J mol−1 and 9503 J mol−1. The respective values for SG were 9037 J mol−1 and 7327 J mol−1. This work demonstrates that mass transfers in D3I are better than those in D2I, and it highlights that, unlike the D2I process, the D3I process is less sensitive to temperature variations, making it particularly advantageous for processing products with high nutritional value.

Preparation and structural characteristics of polysaccharides from loquat peel waste, and their preliminary bioactivities.

Loquat peel, often as food waste, is a valuable source of bioactive polysaccharides. However, study of such polysaccharides is insufficient, leaving a significant gap in understanding their preparation, structure and bioactivities. In this study, three types of loquat peel polysaccharides (LPWP, LPHP and LPNP) were sequentially extracted using hot water, HCl and NaOH solutions, respectively. Among them, LPWP was the purest, with a yield of 3.4% and molecular weight of 470.6 kDa, and it differed from LPHP and LPNP in structure, as evidenced by Fourier transform infrared spectroscopy, X-ray diffraction and scanning electron microscopy, which demonstrated that LPWP consisted of more arabinose (Ara) but less galacturonic acid, rhamnose and galactose, with molar percentages of 71.3%, 23.3%, 3.5% and 1.9%, respectively. Besides, LPWP also exhibited superior antioxidant and antihyperglycemic activities in vitro, particularly in inhibiting α-amylase and α-glucosidase. Methylation and nuclear magnetic resonance analysis confirmed that LPWP was a methyl-esterified pectic polysaccharide rich in branched arabinan, as evidenced by the notable proportion of α-Ara residues, including T-α-Araf, 1,5-α-Araf and 1,2,3,5-α-Araf, with molar percentages of 27.1%, 23.1% and 10.2%, respectively. AFM imaging further revealed its branched-chain morphology and aggregation behavior. This study highlights the potential of loquat peel polysaccharides as a bioactive ingredient with significant antioxidant and antihyperglycemic properties, particularly LPWP, which was found as a methyl-esterified pectic polysaccharide with abundant-branched arabinan. Our work provides valuable insights into the application of loquat peel polysaccharides in functional foods. © 2024 Society of Chemical Industry.

Highly efficient adsorption and removal of phthalate esters by polymers of intrinsic microporosity

In recent years, phthalate esters (PAEs) have been found to be endocrine disruptors that pose a serious safety threat to human health. Currently, adsorption is one of the most efficient technologies to remove PAEs, and the development of adsorbent materials that combine high adsorption capacity and short equilibrium time is a challenging problem. In this study, PIM-1, a typical representative of polymers of intrinsic microporosity (PIMs), was prepared through three methods and first used as adsorbents for PAEs removal. PIM-1 prepared under high temperature (HT-PIM-1) exhibited a high capacity of 787mg/g for dibutyl phthalate (DBP), a prevalent PAE in water, which is significantly higher than most reported adsorbents. Furthermore, more than 90.0% of the equilibrium adsorption capacity can be reached within 30mins. In addition, the adsorption of DBP could be inhibited by ethanol due to the enhanced interaction between DBP and ethanol, which could be revealed by molecular simulation. The adsorption mechanism of PAEs on PIM-1 mainly included hydrophobic interactions, π-π interactions, together with the size matching between PAEs and hierarchical pores of PIM-1. This study provides an idea for the application of PIMs for PAEs removal with high adsorption capacity and high efficiency. Environmental ImplicationPhthalate esters (PAEs) are emerging pollutants that pose a significant threat to public health and safety. They have been detected not only in environmental water but also in alcoholic beverages. Adsorption is widely preferred for removing PAEs, and the adsorption of PAEs in alcoholic solutions is a more challenging process compared to pure water. In this study, PIM-1 with o-phenyl groups similar to PAEs were first used as adsorbents for PAEs and demonstrated a remarkable adsorption capacity in both water (787mg/g) and alcoholic solutions (398mg/g) within a short period, surpassing the performance of commercial adsorbents.

A structural investigation on the interactions of cotton fabric cellulose with olive oil and water

The cotton fabric consists of cellulose arranged in a complex structure with multiple levels of organization at different length scales. Understanding this structure and its interactions with water and oil is essential for developing efficient and environmentally friendly methods of cotton washing. In this study, the structure of raw cotton fabric cellulose and the effects of water and oil were examined across a broad range of length scales using spatially resolved synchrotron small-angle X-ray scattering (SAXS) and auxiliary techniques.Water was observed to penetrate the cotton fabric and interact across nearly all length scales. Although a certain amount of the material was not affected by water as seen by intact distance between microfibrils, fractal analysis of the scattering data indicated a loosening of the microfibril arrangement after contact with water. This process was hindered if the material had been pre-treated with oil and was not seen after subsequent washing with water or surfactant solution. Analyzing spatially resolved SAXS data using a bi-sinusoidal model and 2D maps of the oil-to-cotton ratio facilitates understanding the structure of the material and its interactions with oil on the molecular, nano and macrolevels.

Analysis of wettability and contact angle of sodium bicarbonate impregnated wooden surfaces

Scots pine and spruce wood samples were vacuum impregnated with 3, 5, and 9% sodium bicarbonate solution. Contact angle measurements were made by dropping 0.05 mL of pure water and 3% saltwater solution onto the material’s surface. The surface roughness of each sample was measured, and that of Scots pine control samples was higher than that of spruce samples, but the surface roughness values of spruce wood were higher in the samples impregnated with sodium bicarbonate. When pure water or saltwater solution was dropped onto the samples, it was observed that as the waiting times increased, the contact angle value decreased, the droplet height decreased, and the droplet width increased. It was found that the contact angles were higher in the control samples of both tree species than in the samples of 5% and 7%. The contact angles of 9% impregnation solution, pure water, and salt water were higher than the control samples. As the solution ratio increased on the surfaces impregnated with sodium bicarbonate, the contact angle also increased, and the wettability behavior decreased accordingly. Sodium bicarbonate solution is effectively used in the impregnation process for pine and fir woods, making the materials more resistant to water under outdoor conditions. This solution significantly reduces the risk of deformation of wood by increasing the contact angle and reducing its water absorption properties.

Preservation Potentials of Siderite in Low‐Temperature Brines Relevant to Mars

AbstractThe scarce carbonate record on the Martian surface is one of the fundamental unsolved issues for paleoclimate and environmental evolution. Whether carbonates first formed and then dissolved due to a transition in global environments or whether Mg–Fe carbonates never extensively formed due to geochemical kinetics thresholds remains unknown. In this study, we experimentally examined the preservation potential of siderite in Mars‐relevant fluids, including ultrapure water, H2O2, NaClO4, NaClO3, NaCl, Na2SO4, NaHCO3, and Na2SiO3 solutions, at 277 K. The effects of the water/rock ratio at WR10 and WR100 on dissolution rates were also investigated. We found that siderite dissolution and subsequent oxidation and hydrolysis of leached Fe did not substantially acidify the solutions. The siderite dissolved relatively rapidly in the chloride and chlorate solutions and slowly in the silica or bicarbonate solutions. In a circum‐neutral to slightly alkaline aqueous environment with oxidative species, the mobility of leached Fe was limited, leading to the formation of goethite or lepidocrocite, which clustered on the siderite surface. The longest lifetime of 1‐mm siderite grains was found in the Na2SiO3 solution at WR100, which was estimated to range from 198 ka to 198 Ma. Water‐limited, silica‐rich, and oxidative aqueous environments benefit siderite preservation on the Martian surface. Our results support that the lack of voluminous siderite on Mars may be primarily due to the inhibition of its formation rather than alteration and dissolution after its presence, consistent with the recent detection of Mg–Fe carbonate at Gale Crater and Jezero Crater.

Development of polarizable and hydration-focused water models for the Martini 3 force field

Coarse-grained simulations have been increasingly employed in many fields of molecular chemistry. These models enable the evaluation of complex molecular structures by simplifying their description compared to all-atoms models. Specifically, the Martini 3 force field has been developed to describe biomolecular structures such as proteins, lipids, and carbohydrates. Their “building block” approach has been successfully used in modeling complex systems ranging from carbohydrate solutions, biological membranes, and even deep eutectic solvents. However, one main issue arises when considering interfacial systems: water is represented as a single particle with no effect of electrostatic interactions. In this work, we developed a polarizable water model for the Martini 3 force field, introducing charged particles to model the electrostatic interactions present in water systems accurately. Gaussian Processes were trained with simulation data for both bulk water and cross-interaction parameterization to consistently explore the parameter space and fine-tune our model to the target properties. The developed model showed good performance in reproducing the density and dielectric constant of bulk water. Regarding cross-interaction with other beads, two different sets of parameters were developed. The first, called the polarizable model, is parameterized to reproduce the hydration free energies of the original Martini 3 organic beads. This allows for a good description of free energies of transfer between water and organic phases, the main target property for the Martini 3 force field. The second, called the polarizable-hydration model, is parameterized to match the experimental hydration free energy of selected molecules. This allows for more accurate evaluation of hydration properties, which can be useful for water solutions. In particular, we show that the partitioning and interfacial behavior of nonionic surfactants is improved by the polarizable-hydration model when compared to the standard Martini 3 water model.

The synthesis of polydopamine nano- and microspheres in microdroplets.

Here we developed a microdroplet-based strategy for the rapid synthesis of uniform polydopamine nano- and microspheres. Polydopamine spheres with controllable sizes were generated within hundreds of microseconds by simply spraying water solutions of dopamine into microdroplets. Mass spectrometry revealed that dopamine was primarily oxidized into aminochrome, acting as the major building block for polydopamine. We anticipate that microdroplet chemistry will be rich in opportunities for the synthesis of functional nano- and micromaterials.

Effect of TiO2 nanoparticles on the assembly of a copolymer-clay dispersion

Nanocomposites based on copolymer and clay minerals are attracting increasing attention as they are appropriate for extensive applications. In this work, we present results from an experimental study on the effects of TiO2 nanoparticles on a pluronic-F127/laponite water solution in the sol state. Differential Scanning Calorimetry (DSC), Dynamic Light Scattering (DLS) and Fourier Transform Infrared Attenuated Total Reflection Spectroscopy (FTIR-ATR) were used to characterize the systems. By DSC and DLS measurements the occurrence of micellization was first investigated. The temperature induced self-assembly was then studied by DLS identifying three relaxations associated to differently sized diffusing structures. The correlation between dynamics and bonding structure was thoroughly investigated by analyzing some specific infrared vibrational bands. In particular, the study of the characteristic absorption band of the ether groups in the dry state allowed to evaluate the amorphous/crystalline component evidencing the presence of more extended conformations in presence of the higher TiO2. Finally, the analysis of the bending mode for the residual water provided valuable insight about structural OH groups enabling a distinction between different types of water molecules associated to the copolymer/nanoparticle systems.

Microstructure and properties of a HIP manufactured B4Cp reinforced highly alloyed Al-Zn-Mg-Cu-Zr aluminum matrix composite

In this study, an aluminum matrix composite with good mechanical property and excellent corrosion resistance, B4C particles (B4Cp) reinforced highly alloyed Al-Zn-Mg-Cu-Zr matrix composite, was successfully fabricated through ball-milling, cold isostatic pressing, vacuum degassing, hot isostatic pressing (HIP), homogenization, hot extrusion, solution treatment, and aging treatment. It was found that the B4C/MgAl2O4/Al was the dominant interface structure, which was coherent and enhanced the bonding between the particles and the matrix considerably, while the B4C/Al2O3/Al was the minor interface structure. The grain boundary was very clean in both T4 and T6 aging states, without aging precipitates and O element segregation. In T4 aging state, the composite exhibited superior properties, with the mass density of 2.84 g·cm-3, the elastic modulus of 119.18 GPa, the yield strength of 576.08 MPa, the ultimate tensile strength of 655.27 MPa, the tensile elongation of 1.48%, and the very low electrochemical corrosion current density of 4.4581×10-8 A·cm-2 in 3.5 wt.% NaCl water solution. The MgAl2O4 and BO3-rich interface phases, the strengthening mechanisms and the anti-corrosion mechanisms of the composite were discussed in detail.