Homogeneous Phase Research Articles

Characterization and 3D Reconstruction of the Crushing Behavior of SiO2–CaO–Al2O3–MgO Complex Inclusions in Spring Steel with High Basicity Slag Treatment

This article mainly studies the element content, phase composition, and fragmentation mechanism of SiO2–CaO–Al2O3–MgO composite inclusions that cause fatigue fracture of spring steel. The study found that the SiO2–CaO–Al2O3–MgO composite inclusions in the wire rod are not a homogeneous phase. According to the electron microscopy energy spectrum analysis results, although the SiO2–CaO–Al2O3–MgO composite inclusion is in the low‐melting‐point area of the phase diagram according to the component content ratio. However, field‐emission transmission electron microscopy analysis reveals that this type of composite inclusions includes MgAl2O4, CaAl2Si2O8, CaSiO3, MgSiO3, and a small amount of CaS. The Zeiss Crossbeam 550 electron microscope is used to conduct a three‐dimensional reconstruction analysis of this type of composite inclusions, which once again verified that the composition of this type of inclusions includes calcium silicate, MgAl2O4, MgO, and other phases. It is also found that there is a certain gap between the inclusions and the matrix, and the gap between the inclusions with high‐melting‐points such as MgAl2O4 and MgO and the matrix is more obvious. During the rolling process of SiO2–CaO–Al2O3–MgO composite inclusions, due to differences in hardness and deformation rate between different phases, the rolling process is deformed and fragmented for extended periods.

Mechanical behavior of powdered iron aluminide Fe – 28Al manufactured by direct powder forging

This study examines the impact of direct powder forging of powders on the composition, structure, and mechanical properties of iron aluminide Fe–28 at. % Al. During the synthesis and forging of Fe3Al powders, a homogeneous A2 phase is formed at a temperature of 1100 °C. Porosity after forging is 2–2.5 %. Residual pores are predominantly planar in shape and are located at the boundaries of the powder particles. Annealing at 1300 °C improves the quality of interparticle boundaries and all samples exhibit transcrystalline fracture mechanism. Samples forged at 1100 °C and annealed at 1300 °C show maximum strength σbend = 1050 MPa and fracture toughness K1c = 32.3 MPa·m1/2. The yield strength demonstrates anomalous temperature sensitivity with a maximum of 400 °C and at 500 °C. Samples tested at 600 °C show a decrease in yield strength, but a high enough yield point σy ∼400 MPa and a high strengthening rate are very important for high-temperature creep resistance. In creep experiments at a load of 120 MPa at 600 °C, the strain rate varies in the range of 10−7–10−6 s−1, the value of the rate sensitivity n ≈ 4. The main mechanism of creep is dislocation glide.

Raman Spectroscopy Investigations of Ribbeck Meteorite.

On 21 January 2024, asteroid 2024BX1, discovered the three hours before, fell to Earth south of Ribbeck in the Havelland region of Germany. In this study, fragments of the Ribbeck meteorite, characterized by white and gray colors lithology, were examined for their chemical and phase compositions. The white lithology fragment exhibited a homogeneous chemical and phase structure typical of orthopyroxene, which crystallizes in the orthorhombic system. The gray lithology fragment showed a greater diversity in chemical and phase compositions. Raman spectra analysis revealed that, in addition to the pyroxenes found in the white lithology fragment, minerals from the olivine group (fayalite and forsterite) were also present, along with plagioclase and sulfur in pure crystalline form.

Transported Entropy of Ions and Peltier Coefficients in 8YSZ and 10Sc1CeSZ Electrolytes for Solid Oxide Cells.

In this study, the transported entropy of ions for 8YSZ and 10Sc1CeSZ electrolytes was experimentally determined to enable precise modeling of heat transport in solid oxide cells (SOCs). The Peltier coefficient, crucial for thermal management, was directly calculated, highlighting reversible heat transport effects in the cell. While data for 8YSZ are available in the literature, providing a basis for comparison, the results for 10Sc1CeSZ show slightly smaller Seebeck coefficients but higher transported ion entropies. Specifically, at 700°C and an oxygen partial pressure of pO2=0.21 bar, values of SO2-*=52±10 J/K·F for 10Sc1CeSZ and SO2-*=48±9 J/K·F for 8YSZ were obtained. The transported entropy was also validated through theoretical calculations and showed minimal deviations when comparing different cell operation modes (O2||O2-||O2 and H2, H2O||O2-||O2). The influence of the transported entropy of the ions on the total heat generation and the partial heat generation at the electrodes is shown. The temperature has the greatest influence on heat generation, whereby the ion entropy also plays a role. Finally, the Peltier coefficients of 8YSZ for all homogeneous phases agree with the literature values.

Insight into the Cationic Charge Distribution in U1-y-zPuyAmzO2±x Mixed Oxides.

Uranium-plutonium mixed oxides, containing few mol % of Am, are currently studied as fuel for Sodium Fast Reactors. The study of the O/M ratio of these fuels is of main interest, as its variation can induce issues for reactor safety. For this purpose, four U1-y-zPuyAmzO2±x samples (0.235 ≤ y ≤ 0.39 and 0.005 ≤ z ≤ 0.02) were studied using electron probe microanalysis (EPMA), X-ray powder diffraction (XRD), and X-ray absorption spectroscopy (XAS) experiments. EPMA analyses revealed a homogeneous matrix phase with few U- and Pu-rich agglomerates. A matrix phase of fluorite structure (face-centered cubic), as well as a small contribution of a UO2 phase of the same structure, was evidenced for all of the samples by XRD. The O/M ratios of the (U,Pu)O2±x matrix were calculated based on the obtained lattice parameters. XANES experiments highlighted the simultaneous presence of U5+ and Pu3+/Am3+ for all of the samples, indicating a charge compensation mechanism even for stoichiometric samples. Based on the EPMA and XRD results, it was evidenced that this coexistence of U4+, U5+, Pu3+, Pu4+, and Am3+ was not originating from the U- and Pu-rich agglomerates. It was found to be rather a peculiarity of the U1-y-zPuyAmzO2±x matrix phase, discussed with the help of thermodynamic calculations performed on the U-Pu-Am-O system.

Efficient wide-bandgap perovskite photovoltaics with homogeneous halogen-phase distribution

Wide-bandgap (WBG) perovskite solar cells (PSCs) are employed as top cells of tandem cells to break through the theoretical limits of single-junction photovoltaic devices. However, WBG PSCs exhibit severe open-circuit voltage (Voc) loss with increasing bromine content. Herein, inhomogeneous halogen-phase distribution is pointed out to be the reason, which hinders efficient extraction of carriers. We thus propose to form homogeneous halogen-phase distribution to address the issue. With the help of density functional theory, we construct a double-layer structure (D-2P) based on 2-(9H-Carbazol-9-yl)ethyl]phosphonic acid molecules to provide nucleation sites for perovskite crystallization. Homogeneous perovskite phase is achieved through bottom-up templated crystallization of halogen component. The efficient carrier extraction reduces the Shockley-Read-Hall recombination, resulting in a high Voc of 1.32 V. As a result, D-2P-treated device (1.75 eV) achieves a record power conversion efficiency of 20.80% (certified 20.70%), which is the highest value reported for WBG (more than 1.74 eV) PSCs.

Numerical simulation for investigating crevice corrosion of carbon steel in neutral/alkaline concrete construction

Purpose This study aims to investigate the crevice corrosion behavior of carbon steel in neutral/alkaline environments utilizing a transient multi-physics field model. Design/methodology/approach The crevice corrosion of carbon steel with different solution pH and crevice width was modeled, incorporating mass transfer, homogeneous phase and localized electrochemical reactions. The extent of crevice corrosion was evaluated by the geometric deformation of the model mesh. The hydro-chemical state inside the crevice was discussed through the Cl− concentration and potential distribution of the solution. Findings Results revealed that the formation of pitting corrosion near the crevice mouth was accelerated in a neutral solution. When pH = 8 and pH = 9, the carbon steel matrix was dissolved and the Cl− content within the solution was significantly reduced due to the higher concentration of hydroxide ions (OH−). Originality/value The crevice corrosion behavior of carbon steel in neutral/alkaline environments is closely associated with solution pH rather than the crevice width. The inhibition of crevice corrosion in alkaline environments was proved by finite element simulation. These findings provide valuable insights that can be applied in engineering applications to prevent and mitigate crevice corrosion in neutral/alkaline environments.

Scalable Synthesis of Organic Core/Shell Architectures toward Dual-Wavelength Optical Waveguides.

Organic core/shell heterostructures have undergone rapid progress in materials chemistry owing to the integration of a wide array of unique properties. Nonetheless, the intricate challenge of regulating homogeneous nucleation and phase separation processes in excessively analogous cocrystal structures presents a formidable barrier to expanding the synthesis strategy for organic core/shell heterostructures. Herein, we successfully achieved a phase separation growth process facilitated by the organic alloy interface layer through a dynamic visualization to capture the intricate morphological evolution. By finely regulating the nucleation process, homogeneous self-assembly induced by high chemical and structural compatibility is circumvented, enabling the formation of organic core/shell heterostructures. Notably, this core/shell architecture boasts dual-wavelength emission at 496 and 696 nm, accompanied by an optical loss coefficient of 0.092 dB per micrometer. This methodology shows potential for extending to the scalable design of other conformational cocrystal heterostructure systems, thereby offering valuable insights into the realm of organic photonics.

Growth-phase-dependent control of rRNA synthesis in Saccharomyces cerevisiae.

Saccharomyces cerevisiae is one of the most well-studied model organisms used in the scientific community. Its ease of manipulation, accessible growth conditions, short life cycle, and conserved eukaryotic metabolic pathways make it a useful model organism. Consequently, yeast has been used to investigate a myriad of phenomena, from microbial to human studies. Most of the research performed using this model organism utilizes yeast cell populations when they are growing exponentially, a growth phase aptly termed exponential or log phase. However, log phase encompasses several yeast generations and ranges several hours of yeast growth, meaning that there is a potential for variability during this "homogenous" growth phase. Cells in log phase require robust ribosome biogenesis to support their rapid growth and cell division. Interestingly, during log phase, ribosomal RNA (rRNA) synthesis (which is the first and rate limiting step in ribosome biosynthesis) has been shown to decrease prior to growth rate decline in stationary phase. In this study, we utilized several genomic and biochemical methods to elucidate the relationship between subphases of log phase and rRNA synthesis. Our results indicate that as yeast cells progress through subphases of log growth, both polymerase I transcription and rRNA processing are repressed. Overall, this study establishes a growth-phase-dependent control of rRNA synthesis that unexpectedly begins prior to the switch to stationary phase (i.e., pre-diauxic shift) as a putative mechanism of anticipating nutrient starvation.IMPORTANCESaccharomyces cerevisiae is a ubiquitously used model organism in a wide range of scientific research fields. The conventional practice when performing yeast studies is to investigate its properties during logarithmic growth phase. This growth phase is defined as the period during which the cell population doubles at regular intervals, and nutrients are not limiting. However, this growth phase lasts hours and encompasses several yeast cell generations which consequently introduce heterogeneity to log growth phase depending on their time of harvest. This study reveals significant changes in the transcriptomic landscape even in early stages of exponential growth. The overall significance of this work is the revelation that even the seemingly homogenous log growth phase is far more diverse than was previously believed.

Superior strain-hardening and strength-ductility synergy by hierarchical L12 phases in a highly (Al, Ti)-added medium-entropy alloy

A novel precipitate-strengthened Co–Cr–Ni medium-entropy alloy with a pure “FCC + L12” dual-phase structure is developed by adding a high concentration (6 at.%) of Al and Ti elements. After aging heat treatment at 700 °C for 4 h, the hierarchical L12 phases, composed of primary large-sized L12 phases (∼70 nm) and secondary L12 particles (∼14 nm), are achieved. The designed alloy featuring hierarchical L12 phases exhibits excellent strength-ductility combinations and strain-hardening ability, properties that are much improved over their counterparts with homogeneous dispersed L12 phases (∼13 nm) and without L12 phases. Especially, the yield strength (1320 MPa), ultimate tensile strength (1886 MPa), and average strain-hardening rate (5.15 GPa) are obtained in the alloy with hierarchical L12 precipitates deformed at cryogenic temperature. The Orowan bypass mechanism of the primary L12 phases, along with the shearing mechanism of the secondary L12 phases, collectively contributes to the exceptional strength of the alloy with hierarchical L12 precipitates. The penetration of dislocations and stacking faults (SFs) in the primary L12 phases, combined with hetero-deformation-induced (HDI) hardening attributed to these hierarchical L12 precipitates, may be a key factor in improving strain-hardening properties of the alloy.

Structure and magnetostriction in Nd0.25Tb0.3Dy0.45 (Fe0.9B0.1)1.93 compound

We investigate the structural, magnetic, and magnetostrictive properties of a Nd-containing Nd0.25Tb0.3Dy0.45(Fe0.9B0.1)1.93 (NTDFB) alloy. X-ray diffraction and electron backscatter diffraction analyses reveal that NTDFB exhibits a homogeneous Laves phase, contrasting with the multiphase nature of the boron-free counterpart. At room temperature, the spontaneous and saturation magnetostrictions of NTDFB are 2094 ppm and 1447 ppm, respectively, representing enhancements of 15.9% and 29.5% compared to boron-free samples. Another intriguing finding is that the introduction of Nd effectively alters the spin reorientation temperature of Terfenol-D (Tb0.3Dy0.7Fe1.93) and narrows the temperature span of easy magnetic direction (EMD) along < 100 > . NTDFB undergoes two spin reorientations, with the EMD transitioning from < 111 > to < 100 > at TSR1 173 K and from < 100 > to < 110 > at TSR2 92 K, contrasting with TSR1 245 K and TSR2 25 K of Terfenol-D. Additionally, the introduction of Nd into Terfenol-D effectively increases its magnetostriction coefficient,λ110 and λ100. As a result, NTDFB, with a raw material cost 80% that of Terfenol-D, exhibits magnetostriction values exceeding 1000 ppm from 300 to 20 K, indicating its cost-effectiveness and promising potential as a magnetostrictive alloy.

Short DNAzymes for Efficient Catalysis of "Click" Reactions in Solution and on Surface.

We have systematically investigated and found surprising superior catalytic activities of very short DNAzymes for copper(I)-catalyzed azide-alkyne cycloaddition (CuAAC), both in solution and on surface. As a key reaction of the "click chemistry" class, CuAAC is a highly efficient and specific covalent conjugation tool with demonstrated applications in organic synthesis, bioconjugation, and surface functionalization; however, it requires the presence of the Cu(I) catalyst, which is an unstable species in aqueous solutions. We show here that one ultrashort, 14-nucleotide-truncated fragment of an earlier in vitro selected DNAzyme (CLICK-17) shows a striking and superior catalytic activity toward the in trans CuAAC reaction in solution and on surface in the presence of either Cu(I) or Cu(II), at significantly lowered concentrations. These results obviate the need for long-sequence DNAzymes, selected out of the homogeneous solution phase, for application in complex surface environments.

Rapid Peracetic acid activation by CoO under neutral condition: The contribution of multiple reactive species

This paper proposes a novel process of cobalt monoxide (CoO)-activated peracetic acid (PAA) for treating emerging micropollutant in water. PAA was activated under neutral conditions by combining a dominant heterogeneous phase on the catalyst surface and a homogeneous phase by dissolved Co2+. The system produced several reactive oxygen species, including hydroxyl radicals (HO∙HO•), singlet oxygen (1O2), organic radicals (RO•(CH3C(O)O•, CH3C(O)OO•) and high-valent cobalt (Co(IV)). Organic radicals and high-valent cobalt primarily drove the emerging micropollutants degradation, interacting via electron transfer. Further density functional theory calculations supported that the spontaneous adsorption of PAA onto the catalyst could break peroxy bonds that generate radicals. Furthermore, the CoO surface structure underwent minimal changes during the reaction, making it highly reusable. Thus, the novel CoO/PAA system could be an effective advanced oxidation process for water treatment.

Synthesis and characterization of epoxy resin‐polydicyclopentadiene interpenetrating polymer networks by UV‐initiated simultaneously frontal polymerization

AbstractBy combination of UV curing and frontal polymerization, interpenetrating polymer networks (IPNs) based on diglycidyl ether of bisphenol‐A (DGEBA) epoxy resin and polydicyclopentadiene (PDCPD) were prepared by UV‐induced simultaneously frontal polymerization in this paper. Compared with the net DGEBA cured polymer, the tensile strength, elongation at break and impact strength of the IPNs were simultaneously improved. The maximum tensile strength and elongation at break of the IPNs reached 100 MPa and 4.64%, respectively, and the maximum impact strength reached 7.34KJ/m2 with an improvement of 115.2% over that of the net DGEBA cured polymer. Thermogravimetric analysis (TGA) results revealed that the IPNs could enhance the thermal stability. Data of the differential scanning calorimetry (DSC) and TGA testing shows that the IPN shows a single glass transition temperature (Tg) which is between the Tg of DGEBA and DCPD, indicating homogeneous phase and highly cross‐linked IPN formed. Morphologies and molecular structure of the IPNs polymer were observed by scanning electron microscope (SEM) and characterized by Fourier transform infrared spectroscopy (FTIR), respectively, whose results also proved the formation of ideal IPNs structures.

Physical properties of tween 20 + di-potassium hydrogen phosphate anhydrous (or tri-potassium phosphate 1,5-hydrate) + water from 288.15 K to 318.15 K

ABSTRACT The present study investigates the characterisation of binary and ternary mixtures involving a surfactant such as Tween 20 and various potassium salts in aqueous solutions. The ternary mixtures can form two distinct immiscible liquid phases. Several physical properties, including refractive index, density, and speed of sound, were measured, and derived properties such as excess molar volume and isentropic compressibility were calculated. The research focuses on the behaviour of aqueous binary and ternary mixtures composed of Tween 20, salts (di-potassium hydrogen phosphate anhydrous and tri-potassium phosphate 1,5-hydrate), and water in their homogeneous phases. It examines the influence of the surfactant and salts and the effect of temperature on these physical properties for homogeneous mixtures. Additionally, the physical properties of the equilibrium phases were determined to cover all the homogeneous zones comprehensively.

Liquid-liquid equilibrium of FAEs – glycerol phase – ethanol in the ethanol regeneration and FAE separation stage

Extraction and purification of biofuel components are as important as their synthesis. Synthesis of fatty acid esters in a molar excess of ethanol above 1:30 results in the formation of a homogeneous phase including the ester and glycerol phases dissolved in ethanol. It was observed that when excess ethanol was removed, the separation of the system into ester and glycerol phases did not always occur. To improve the biodiesel purification process the experimental binodal curve for the FAE-ethanol-glycerol phase system was obtained in the synthesis of biodiesel from rapeseed oil. The data was obtained from homogeneous alkaline synthesis of FAE with molar excess of ethanol 1:50. The pseudocomponent glycerol phase contains glycerol and unreacted oil (triglycerides (TGA)). The calculated liquid-liquid equilibrium (LLE) data for FAE – ethanol – glycerol and FAE – ethanol – TGA ternary mixtures were obtained by the UNIFAC (UNIQUAC Functional-group Activity Coefficients) model and compared with experimental diagram. It was found that glycerol and unreacted triglycerides affect the behavior of the system by preventing or promoting the mixing of immiscible components. The obtained results show that, depending on the conversion, the phase behavior of the FAE-ethanol-glycerol phase system will correspond to the ternary system FAE-ethanol-glycerol or FAE-ethanol-TGA. The obtained data help to predict the separation of glycerol and ester phases at the ethanol recovery stage knowing the degree of rapeseed oil conversion at the synthesis stage. Successful separation of the glycerol and FAE phases is possible at oil conversion above 53 %.

The effect of various Sn and Ca equal proportional addition on the microstructure, mechanical behavior and corrosion performance of Mg alloys

In the present study, the effects of various Sn and Ca equal proportional addition (0.3:0.1, 0.6:0.2, 1.2:0.4, wt%) on the microstructure, mechanical properties and corrosion behavior of Mg-Sn-Ca alloys were systematically investigated. With the increase of Sn and Ca content, microstructure uniformity of the Mg-Sn-Ca alloy was improved, the average grain size was refined (from 34.4 μm to 21.62 μm, 13.47 μm), and more CaMgSn phases were generated (from 0.39 % to 1.64 %, 4.53 %). With increasing Sn and Ca content, the tensile yield strength (TYS) and ultimate tensile strength (UTS) of Mg-Sn-Ca alloys were gradually increased (TYS: from 91.8 MPa to 98.24 and 125.05 MPa; UTS: from 187.48 MPa to 190.73 and 214.58 MPa), mainly due to the contribution of grain refinement. The electrochemical tests revealed that the corrosion resistance of the Mg-Sn-Ca alloy initially decreases and then increases with the increase of Sn and Ca contents. The hydrogen evolution volume of Mg-0.3Sn-0.1Ca alloy was 41.91 mL cm−2, and the corrosion current density was −1.54 × 10−3 A/cm2. As for Mg-0.6Sn-0.2Ca alloy, deteriorated corrosion resistance compared to the Mg-0.3Sn-0.1Ca alloy was mainly ascribed to the micro-galvanic corrosion between the CaMgSn phase and Mg-matrix. The Mg-1.2Sn-0.4Ca alloy had the best corrosion resistance, with the lowest hydrogen evolution volume of 34.09 mL cm−2 and a minimum current density of −1.15×10−3 mA cm−2, its high corrosion resistance could be attributed to the grain refinement and homogenous distributed CaMgSn phase and more generated Ca(OH)2 product film with dense-structure.

Heterogenization of Homogeneous Donor-Acceptor Conjugated Polymers for Efficient Photooxidation: An Approach Toward Sustainable and Recyclable Photocatalysis.

Recovery of homogeneous photocatalysts from reaction mixture is challenging, affecting the cost-effectiveness, and masks their advantages, including 4-8 fold higher catalytic activity than corresponding heterogeneous counterparts. Incorporation of long alkyl chains within the rigid π-conjugated backbone of conjugated polymers can augment their solubility in particular organic solvents; accordingly, they can function as homogeneous photocatalysts. Consequently, these polymers facilitate the recovery of catalysts through the reverse dissolution process, thus creating a well-suited platform to meet certain advantages of both homo- and heterogeneous photocatalysts. This work exemplifies the unprecedented perks of donor-acceptor conjugated polymers from benzodithiophene and substituted dibenzothiophene sulfone moieties for their homogeneous phase photoredox activities along with their heterogeneous recovery and reuse up to five runs. The potential intermediate singlet oxygen (1O2) and superoxide (O2•-) as reactive oxygen species generated by these photostable conjugated polymers efficiently catalyze the visible-light-driven oxidation of aryl sulfides (up to 92% yield) and oxidative hydroxylation of phenylboronic acids (up to 93% yield), respectively. Therefore, to actualize the heightened catalytic performance and formulate a design strategy for polymeric photoredox catalyst, our work introduces an alternative approach to the advancement of photocatalysis with diverse catalytic activities.

Phase behavior of the carbon dioxide/toluene/poly(ethylene glycol) ternary system

The phase behavior of a carbon dioxide (CO2)/toluene (Tol)/poly(ethylene glycol) (PEG) ternary system was investigated in this study to consider the effect of the polymer species on the phase diagram. Measurements were performed using a synthetic method combined with laser displacement and turbidity measurements. Bubble points (vapor–liquid phase separation) were determined from changes in the piston displacement and cloud points (liquid–liquid (LL) phase separation) were determined from changes in the turbidity. The phase boundaries of the CO2 mass fractions ranging from 0.113 to 0.496 were measured by varying the Tol/PEG mass ratio. The homogeneous phase area decreased when the mass ratio of PEG to Tol increased and/or the temperature decreased. These changes in the LL phase-separation behavior were explained by referring to the free volume fraction and solubility parameter estimated using the Sanchez–Lacombe equation of state. The free volume integral fraction could explain the phase diagram, but not the solubility parameter; the effect of polymer species on the Px phase diagram of the ternary system was explained by considering specific interactions between dissimilar components. These results could promote a comprehensive understanding of the phase diagram of CO2/organic solvent/polymer systems and aid the prediction of phase behavior.

Numerical investigation into the influence of interfacial transition zone on elastic modulus, creep, shrinkage of concrete

Interfacial transition zone (ITZ) is a weak part around aggregate in concrete, which could threaten the macroscopic properties of concrete such as strength, stiffness, deformation, and durability. However, it is difficult to quantify the ITZ effect on the macroscopic behavior of concrete only by experimental methods due to the tiny thickness of ITZ. This study employed finite element (FE) method to investigate the ITZ effect on the elastic modulus, creep, and shrinkage. A mesoscale three-phase FE model consisting of homogeneous matrix phase, aggregates and ITZ around them was developed for concrete in this study. The influences of the FE model dimension and the meshing size on the calculated results were first discussed. Then the influence of the thickness, viscoelasticity and shrinkage of ITZ on the macroscopic properties of concrete were evaluated based on the FE calculation and grey relation analysis. Finally, the measured elastic modulus, creep and shrinkage of concrete with different contents of clay on coarse aggregates were used to validate the FE model. It is found that the calculated results of the two-dimensional (2D) FE model are in good agreement with those of the three-dimensional (3D) FE model under the linear viscoelastic assumption. The meshing size has a minor effect on the calculated results when it is 0.2–2 times of the ITZ thickness. The influence of ITZ properties on the macroscopic properties of concrete will become more significant as the ITZ thickness increases. Moreover, the elastic modulus of ITZ has a greater impact on the effective properties of concrete than the thickness, creep, and shrinkage of ITZ. The findings in study can contribute to a better understanding of ITZ effect on the macroscopic properties of concrete and provide references to the reasonable consideration of ITZ in numerical studies.