Phase Transformation Process Research Articles

Solid‐Solid Phase Transformation Behavior of ϵ‐CL‐20 Induced by Typical Organic Solvents: A Theoretical and Experimental Study

AbstractThe solid‐solid phase transformation of ϵ‐CL‐20 induced by external conditions is one of the bottlenecks limiting the widespread applications of CL‐20‐based energetic materials. Herein, we report the investigation on the influence of solvent polarity on ϵ‐CL‐20 solid‐solid phase transformation behavior both theoretically and experimentally. Density functional theory (DFT) calculation was performed to evaluate the possibility of ϵ‐CL‐20 phase transformation induced by organic solvent molecules from the perspective of ϵ‐CL‐20 electronic structure and molecular structure variations. Additionally, experimental study of ϵ‐CL‐20 phase transformation induced by 1,2‐dichloroethane, ethanol, and methanol gas environment was conducted. Solvent with higher polarity was confirmed to significantly vary molecular surface electrostatic potential and molecular conformation of ϵ‐CL‐20 molecule. Furthermore, ϵ‐CL‐20 critical phase transformation temperature decreased when using inducing solvent with higher polarity. And the observed maximum phase transformation rate was the one induced by the highest polarity solvent. A four‐parameter model was established to describe the phase transformation process as a function of time based on the experimental results. Possible ϵ‐CL‐20 solid‐solid phase transformation mechanism was proposed. Hopefully, these results will be beneficial for the rational preparation and utilization of CL‐20‐based energetic materials.

The change of phase composition and the morphology of particles of hydrothermal titanosilicate precipitates during their aging

During the study of phase formation under conditions of hydrothermal synthesis of alkaline titanosilicate systems (NH₄)₂TiO(SO₄)₂⋅H₂O или TiOSO₄⋅H₂O-Na₂SiO₃-NaOH-H₂O it was found that the formed titanosilicate solid phases differ both in composition and structure. The process of their aging under conditions of long-term exposure without forced heating is accompanied mainly by the loss of free water without noticeable structural and morphological changes. The exposure to the temperature of 70–100°С significantly accelerates the process of solid phase transformation. In these conditions, a porous system of particles is formed, which is confirmed by an increase in their specific surface area and total pore volume, as well as by an increase in the activity of the powders to absorb single- and double-charged cations. The effectiveness of hydrochloric acid treatment of fresh and especially aged precipitates on the ordering of the structure with the formation of crystals of a clear frame shape, inherent in the minerals zorite and ivanyukite, which contributes to increasing the sorption capacity of the final product is shown. The obtained results are used to adjust the technological regulations, which are used to test the technology of titanosilicate sorbent on the pilot plant.

A microscale cellular automaton method for solid-state phase transformation of directed energy deposited Ti6Al4V

Directed energy deposition is a promising additive manufacturing technology that fabricates complex geometries by fusing feed material layer-by-layer. However, the formation mechanism of the directed energy deposited Ti6Al4V solid-state phase transformation process, which is crucial for understanding the process-structure–property relationship, has remained unclear. In this study, a microscale cellular automaton method is proposed to simulate the microstructure evolution process for Ti6Al4V, specifically the β→α/α′ phase transformation process within a few β grains. The method is further integrated with the mesoscale cellular automaton method, which predicts the prior β grain structure, the solid-state phase transformation kinetics model for the prediction of the phase volume fractions, and the finite volume method, which is used for the thermal-fluid flow modelling, providing a temperature field to the former. The integrated numerical framework not only links the thermal history with the phase volume fractions but also provides the columnar β grain structures and acicular α/α′ grain structures in satisfying agreement with the available experimental observation. Moreover, the predictions shed some light on the formation mechanism of the hierarchical α/α′ structure and their particular clusters. The influence of the cooling rate on the α/α′ grain formation is illustrated via the three-layer case simulation. The findings on the formation mechanism of α/α′ are beneficial in tailoring the microstructure of Ti6Al4V for excellent mechanical properties in directed energy deposited Ti6Al4V.

A lightweight semi-active ankle exoskeleton utilized NiTiCu-based shape memory alloys for energy storage.

Nowadays, exoskeletons have a place in many fields, such as industrial production, medical rehabilitation, and military. However, there are still many shortcomings in the existing exoskeleton, such as heavyweight and complex structures for active exoskeleton. The driving ability of passive exoskeletons is limited. To reduce the energy consumption of wearers, based on the characteristics of the semi-active ankle exoskeleton, this paper proposes to use NiTiCu-based shape memory alloys (SMA) as the energy storage source to improve the power density. Compared to NiTi-based SMA, the phase transformation process of NiTiCu-based SMA is more rapid, which can solve the response delay problem to a certain extent. The ankle exoskeleton uses SMA deformation to compress the bias spring. When the human ankle joint needs auxiliary torque, the SMA releases the energy stored by the bias spring and transfers the energy to the ankle exoskeleton to achieve the effect of assisting the human ankle joint. During the assistance process, a control system based on the SMA mathematical model is constructed. The above-mentioned ideas provide a new approach for further expanding power density and can be widely applied in the field of robotics. During characterization, this semi-active ankle exoskeleton can effectively complete the movement state of upstairs and walking, achieve an effective power of 180 N, and store maximum energy up to 5J for the human ankle.

Effect of Mo on the Phase Transformation, Microstructure, and Hardness of Q500qENH Weathering Steel of Bridge Construction during Continuous Cooling

This article investigates the precipitation behavior of Mo element in the continuous cooling phase transformation process of weathering steel of bridge construction and its influence on microstructure and hardness. The results demonstrate that the addition of Mo leads to the narrowing of the phase transformation interval of proeutectoid ferrite and pearlite, the expansion of the bainite transformation zone, a delayed bainite phase transformation process, and the refinement of bainite microstructure. Moreover, theoretical calculations of bainite phase transformation kinetics reveal that the average activation energy for bainite transformation in Mo‐free and Mo‐containing steels is 94.8 and 134.0 kJ mol−1, respectively. The new grains of Mo‐free steel mainly grow in a 2D mode, while Mo containing steel mainly grows in a 1D mode, which confirms the retarding effect of Mo on bainite grain growth. Additionally, Mo significantly increases the number density and refines the size of precipitated phases in weathering steel of bridge construction. Within the cooling rate range of 0.1–30 °C s−1, the hardness of weathering steel of bridge construction is enhanced by Mo, with the magnitude of hardness increment decreasing as the cooling rate increases. This behavior is primarily governed by the combined influence of phase transformation strengthening and precipitation strengthening.

Adsorption characteristics of As(III) by schwertmannite: new findings in mineral-phase transformation and microbial effects

The amount of As(III) adsorbed and the interfacial process are closely associated with the phase transformation of Schwertmannite (SCH). At present, studies on the adsorption characteristics of As(III) on SCH and the accompanying phase transformation process, especially the related mechanisms under the mediation of iron-reducing bacteria (FeRB) and sulfate-reducing bacteria (SRB), are limited in existing literature. With the help of continuous characterization, the adsorption behavior of As(III) on SCH was explored, as well as the transformation processes of SCH during these processes. The findings revealed that the SCH, synthesized by the KMnO4 oxidation and ethanol modification methods, exhibited excellent physical adsorption capacity for As(III) due to their increasing specific surface area and porosity. At room temperature (20°C), the saturation adsorption capacities of As(III) by M-SCH and Y-SCH reached 62.69 and 58.62 mg/g, respectively. Moreover, the generation and phase transformation of As(III)-bearing ferrihydrite were observed within a 60-min timeframe. It is the first time this phenomenon has been observed in such a short time, which is presumed to be an intermediate stage in the transformation of SCH into goethite. Furthermore, both FeRB and SRB could enhance the adsorption capacity of SCH for As(III). Comparatively, SRB has a more substantial impact on SCH’s phase transformation. These insights are valuable for the practical application of SCH in treating As(III) pollution.

Synthesis and Local Characterization of CoO Nanoparticles in Distinct Phases: Unveiling Polymorphic Structures.

The advancement of functional nanomaterials has become a major focus of recent research, driven by the exceptional properties these materials display compared to their macroscopic (bulk) counterparts. Cobalt oxide nanoparticles (CoO-NPs) stand out primarily for their catalytic and magnetic properties, which can enable a range of technological applications, such as advanced catalysts, drug delivery systems, implants, prosthetics, sensors. However, in addition to the dependence on factors such as size, morphology, and functionalization, the properties of CoO-NPs are significantly influenced by the crystal structure. Therefore, local investigation into the polymorphic structures of CoO at the nanometric scale may provide new insights into the local structural and magnetic characteristics of these systems. In this report, we address the synthesis and local characterization of cobalt oxide (CoO) nanoparticles in the rock-salt cubic fcc-CoO and Wurtzite hpc-CoO phases, obtained through thermal decomposition. We analyze the influence of oleylamine and oleic acid ligands on the structural and morphological control of these systems. The obtained nanoparticles were characterized using conventional techniques such as X-ray diffraction (XRD), transmission electron microscopy, Raman spectroscopy, and Fourier-transform infrared spectroscopy. Local characterization was carried out by the perturbed angular correlation (PAC) nuclear technique using the radioactive tracer 111In(111Cd). Measurements were conducted at 295 and 10 K to investigate possible magnetic phase transitions in these systems. XRD results confirmed the formation of fcc-CoO and hcp-CoO phases. The phase fcc was obtained with the pair of oleylamine and oleic acid ligands, while the phase hcp phase was synthesized using only oleylamine. Additionally, nanoparticles synthesized with oleylamine and oleic acid exhibited better morphological control compared to those produced with only oleylamine. Raman spectroscopy analyses suggest a phase transformation process resulting in Co3O4. PAC results for hyperfine interactions at the 111In(111Cd) probe nucleus, indicate that the hcp-CoO phase shows smaller hyperfine magnetic interactions (B hf = 1 T) compared to the fcc-CoO phase (B hf = 17 T). This suggests the mechanism of superexchange interactions, which are strongly influenced by the Co-O-Co bond angle, which is 110° for the hpc-CoO phase and 180° for the fcc-CoO phase due to the geometries of the systems.

Austenite-martensite interfacial patterns and energy dissipation of phase transformation in Ni-Mn-Ga single crystal

The martensitic phase transformation occurs in Shape Memory Alloys (SMA) via the nucleation/propagation of the Austenite-Martensite interface (A-M interface), which is a transition region (domain) between the two coexisting phases. For providing compatibility, the transition region consists of various martensitic twin structures (laminates), forming different interfacial patterns, such as parallel laminates and branching laminates. Due to the energy accumulation in the interfacial structures (e.g., elastic mismatch and twin-boundary surface energy), the interfacial patterns should be relevant to the driving force (energy dissipation) and the associated kinetics of the phase transformation. In this paper, we adopt a special thermal loading, small-temperature-gradient “heating-cooling-reheating”, to control the A-M interface's forward and reverse propagation to generate different interfacial patterns in a Ni-Mn-Ga single crystal SMA with the observation on the twin structures (by optical microscope and SEM) and the InfraRed measurement on the temperature hysteresis of the interface propagation (for characterizing the thermal driving force). Simple energetic analysis indicates that the thermal driving force (energy dissipation) is directly related to the stored energy in the interfacial structure, particularly the large mismatch elastic energy near the habit plane. This study not only provides the details of the various interfacial patterns and their dependence on the loading path, but also indicates the driving force and the associated mechanism about the pattern evolution to understand the phase transformation process.

Solute and phase heterogeneous distribution at different scales and its effect on ageing physical phenomena in a laser powder bed fusion produced maraging steel

The Laser Powder Bed Fusion process involves complex thermodynamic and heat transfer mechanisms which results in a complicated understanding of the material’s microstructure and phase transformation processes. In the case of additive manufacturing maraging steels, these present heterogeneous structures which mainly consist of Body-Centred Tetragonal (BCT) martensite and retained austenite (Face-Centred Cubic (FCC) phase structure), unlike conventionally processed material. Research has already been done on the competitive or collaborative nature of austenite growth/reversion and precipitation in these materials. However, for Laser Powder Bed Fusion maraging steels, studies have focused on either the effect of the heterogeneous structures on austenite reversion kinetics or the formation, evolution and behaviour of precipitation. Still, no comprehensive research exists that covers in detail the relation between solute heterogeneity from the meso- to the nanoscale and its influence on both phase distribution and ageing physical phenomena. To do so, multiscale chemical analyses and microstructural characterisation techniques were used to investigate a maraging steel M300 in different transformed conditions: as-built, aged at 480 and 540 °C. The results showed that competing mechanisms during printing caused segregation at the mesoscale, which remains in aged samples. Vaporisation led to Cr segregation, while melt convections caused Ni and Ti depletion at melt pool boundaries. Retained austenite location was found at melt pool boundaries and away from them on the as-built structure. Its preferential location remains unclear. Dissimilarities from conventional material were identified in nanosized clustering and precipitates on aged samples.

Phase transformation in titanium alloys: A review

Due to a series of exceptional properties, titanium and titanium alloys have received extensive attention in recent years. Different from other alloy systems, there are two allotropes and a sequence of metastable phases in titanium alloys. By summarizing the recent investigations, the phase transformation processes corresponding to the common phases and also some less reported phases are reviewed. For the phase transformation only involving α and β phases, it can be divided into β→α transformation and a reverse transformation. The former one has been demonstrated from the orientation relationship between α and β phases and the regulation of α morphology. For the latter transformation, the role of the stress has been discussed. In terms of the metastable phases, the mechanisms of phase formation and their effects on microstructure and mechanical properties have been discussed. Finally, some suggestions about the development of titanium alloys have been proposed.

Hydrogen-based mineral phase transformation of bastnaesite: Detailed assessment of physicochemical properties and flotation behavior

Iron-bearing rare earth ores are valuable mineral resources, and the hydrogen-based mineral phase transformation (HMPT) process has significant development potential. In this study, the changes in physicochemical properties and flotation behavior of bastnaesites subjected to HMPT were investigated. The results show that bastnaesite decomposed slowly below 600 °C, but increased roasting temperature and time enhanced the decomposition, resulting in a roasted product with over 85 % rare earth oxide (REO) grade. HMPT also increased the initial pH of the flotation pulp from about 7.5 to 11.0 and increased La and Ce ion concentrations. By increasing the dosage of SHA, flotation recoveries comparable to the raw ore can be achieved. The HMPT process converted bastnaesite to REOF, which formed complex phases such as Ce7O12 and REF3 when exposed to air. This process resulted in significant damage to the particle structure, increased porosity, reduced geometric particle size, and improved wettability. After HMPT, Ce on the particle surface existed predominantly as Ce4+, which formed Ce(OH)4 precipitation during flotation, inhibiting SHA adsorption. The increased particle porosity facilitated deeper SHA penetration and greater adsorption, resulting in higher SHA dosage compared to the raw ore.

Enhancing strength, ductility, and thermal fatigue resistance in Stellite 21 coatings via Mn alloying and Transformation-Induced Plasticity

This study investigates the effect of Mn on the microstructure and mechanical properties of Stellite 21 cobalt-based coatings prepared by laser cladding on 24CrNiMo steel substrates, focusing on utilizing the Transformation-Induced Plasticity (TRIP) mechanism to enhance toughness and thermal fatigue performance. The results indicate that the microstructure of the Stellite 21 alloy coating is primarily composed of γ-Co (FCC) with a minor presence of ε-Co (HCP), M23C6, and M7C3 carbides, which predominantly precipitate at or near the grain boundaries. Upon the addition of Mn, it dissolves into the γ-Co matrix, causing lattice distortion and increasing dislocation density, thereby contributing to solid solution strengthening. Compared to the Mn-free Stellite 21 alloy coating, the coating with 5% Mn exhibits an approximately 21% increase in tensile strength (∼1135 MPa) and a 74% increase in elongation (∼14.5%). This improvement is mainly attributed to the solid solution strengthening caused by lattice distortion due to Mn addition and the synergistic enhancement from the TRIP mechanism facilitated by the lower stacking fault energy. Moreover, the thermal fatigue crack propagation rate in the coating with 5% Mn is reduced by approximately 42.5% compared to the Mn-free Stellite 21 alloy coating. The enhancement in thermal fatigue performance is primarily due to the Mn addition, which stabilizes the ε-Co phase during thermal fatigue processes, enhancing plastic deformation capacity. The phase transformation process alleviates stress concentration, effectively reducing crack propagation rates and ultimately improving the material's thermal fatigue performance.

Crystal structure stability and phase transition of celsian, BaAl2Si2O8, up to 1100 °C / 22 GPa

Celsian (BaAl2Si2O8) is an important component of aluminosilicate-based ceramics, which is widely used in high temperature/high pressure process. However, limited data available on its high pressure (HP)/high temperature (HT) behavior and HT studies were based on multi-component samples only. Here we present data on crystal structure stability and phase transformation processes of celsian studied under extreme conditions (up to ∼22 GPa/∼1110 °C) using in situ X-ray diffraction. Under HP conditions celsian undergoes three phase transitions: at the pressures below 10 GPa the main changes in the crystal structure of celsian associated with the changes in the coordination Ba-centered polyhedron (celsian-II and celsian-III), whereas at higher pressures AlO4 tetrahedra transforms into AlO6 octahedra (celsian-IV). Though the HP behavior of some isostructural compound has been studied before, the HP transformation of celsian is not similar to any previously studied mineral or synthetic compound. Celsian demonstrate stability and low thermal expansion coefficients (αV = 12 × 10−6 °C−1) in the studied temperature range.

Phase transformation process and toughening mechanism of 12Cr1MoV heat-resistant steel for high-pressure boilers by external shower and internal spray heat treatment

To optimize the heat treatment process for 12Cr1MoV heat-resistant steel, this study designed a novel process of external shower and internal spray (ESIS), followed by air cooling. This new approach was simulated in the laboratory. The study focused on the variation in impact energy and the microstructural changes in the experimental steel subjected to different processes, specifically the T890 and T740 processes (where the numbers represent the termination temperature of ESIS). The phase transformation processes and toughening mechanisms of the steel after these treatments were thoroughly investigated. The theoretical analysis revealed that the microstructures of T890 and T740 steels consist of quasi-polygonal ferrite (QPF), granular bainite (GB), and pearlite. The QPF in T890 steel forms at a higher temperature compared to T740 steel, leading to a lower dislocation density and carbon content in QPF during the subsequent cooling phase. This results in the QPF in T890 steel having a hardness of 1.02 GPa lower than that of the QPF in T740 steel. The higher hardness of QPF in T740 steel correlates with reduced toughness and resistance to crack propagation. Under impact loading, the QPF in T740 steel exhibits insufficient crack propagation resistance to counteract the effects of microscopic defects within the tensile stress region of the fracture. Consequently, cracks preferentially propagate within the QPF, creating a relatively flat propagation path. In comparison, the fracture of T740 steel demonstrates a straighter propagation path in the tensile stress region than T890 steel, resulting in significantly lower impact energy for T740 steel.

SATURATION OF GAS CONCENTRATION SIGNAL OF THE LASER GAS SENSOR

Nowadays it is possible to determine the type of gas with sufficient accuracy when its concentration is less than fractions using spectroscopic methods (optical, radio engineering, acoustic). Along with this, the value of permissible concentrations of explosive, toxic, harmful to technology and ecology gases is practically important. Known physical experimental studies indicate only a linear dependence of the response of a laser gas sensor at units . The research methods for units are based on the processes of combustion, micro-explosion, structural and phase transformations and are not always applicable in real practical conditions. The work is devoted to the analysis of experimentally obtained fluctuations caused by a laser beam in a gas in a photodiode (signal receiver) due to its influence not only at the atomic level, but also on the scale of clusters of nanoparticle molecules. The gas concentration is estimated by the fluctuation-dissipation ratio. It is shown that the signal correlator is saturated to a constant value when the quantum (laser photon energy) and thermal (nanoparticle temperature) factors are comparable with an increase in the concentration of the target gas. The critical values of the saturation concentration are determined by the equality of these two factors.

The interface mechanical and ablative evolution behaviors under different heat flux of multiphase HfC-SiC matrix composites

Multiphase HfC-SiC ceramic matrix composites were prepared by a combination process. The interface mechanics and ablation properties behaviors were investigated. Introducing the PyC-SiC interface, the composites showed a second-order pull-out mechanism. The mechanical failure model showed that fibers and matrix have different failure strain under load depending on the component that fails first. Moreover, the ablative airflow in the center area will spread to the edge area through the thermal shock microcracks generated. Increasing of the heat flux, the crack width gradually increased to be ditches. It accelerated the evolution of surface morphology, which showed HfC-SiC substrate was first transformed into Hf-Si-O solid solution on the process of phase transformation of oxidation products from 1680 ℃ to 2150 ℃, and eventually sintered into HfO2. The change in the morphology of oxidation product consumed more heat and protected the substrate from oxidation, resulting in improving the ablation resistance of composites.

The Investigation of Phase Transformation Process of Nano-Citrogypsum via Recycling Saline Solution

Because citric acid may be used to preserve food, the citric acid business has grown to play a significant role in the food and beverage sector. Environmental problems with gypsum waste, or citrogypsym, resulted from the manufacture of citric acid. Calcium sulfate dihydrate (DH), with low material physical characteristics, is the primary component of gypsum. As a result, the goal of this research is to examine the phase transformation process of citrogypsum using the hydrothermal process, which is a method of recrystallizing an example solution in an appropriate setting. To do this, a recycling calcium chloride solution was used, and it was heated to 95°C for five hours under atmospheric pressure to form alpha calcium sulfate hemihydrate (α-HH). The present of -OH at 1600 cm-1 wave numbers in the FT-IR spectra of α-HH, indicates that CaSO4 has 0.5 water molecules in its crystal. Moreover, the DSC thermograms of α-HH reveal endothermic peaks at 151.2°C and 183.14°C, respectively, which correspond to the loss of 0.5 water molecules in CaSO4. The TGA thermogram of α-HH also shows a crystal water content of 4.5 wt%. Furthermore, SEM images validate the hexagonal structure of α-HH morphology. In addition, because chloride ions have an impact on corrosive materials, the saline solution can be recycled at least four times to save money and the environment.

Enhanced temperature sensing in lead-free Cs3Bi2Cl9 perovskite co-doping Yb3+/Er3+ for optical thermometry application

A simple and rapid grinding method for preparing Er3+-doped and Er3+/Yb3+co-doped Cs3Bi2Cl9 upconversion phosphors was developed. We avoid to employ strong acids as reaction solvents, aligning with the principles of green chemistry. By controlling the thermal treatment temperature and adding BiCl3, a reversible phase transformation process between Cs3Bi2Cl9 and Cs3BiCl6 perovskite phosphors was achieved. The Er3+/Yb3+ co-doped Cs3Bi2Cl9 phosphors emit green light under 980 nm excitation, whereas Cs3BiCl6 phosphors emit red light. Their temperature sensing performance was tested through variable-temperature processes. Compared to Er3+-doped Cs3Bi2Cl9 phosphors, the co-doped Er3+/Yb3+ phosphors have a higher relative sensitivity of 1.60 % K−1. Compared to previously reported materials, Cs3Bi2Cl9 phosphors show enhanced sensitivity in temperature sensing. The study demonstrates that lead-free halide perovskites’ unique color-tunability not only underscores the innovativeness of this synthetic strategy but also provides a significant technological foundation for temperature sensing applications. Given their environmental friendliness and facile preparation process, these phosphors possess notable advantages for industrial production and hold promise as potential candidates for next-generation high-performance phosphor materials.

In-situ scattering and calorimetric studies of crystallization pathway and kinetics in a Cu-Zr-Al bulk metallic glass

The crystallization route and kinetics of a Cu-Zr-Al bulk metallic glass (BMG), based on Cu50Zr50, were investigated using in-situ synchrotron small- and wide-angle X-ray scattering (SAXS/WAXS), in-situ high-energy X-ray diffraction (HEXRD), and differential scanning calorimetry (DSC). The acquisition of kinetic diagrams of SAXS/WAXS enables the direct construction of the overall phase transformation route from room temperature to the onset temperature of solid state phase transformation upon heating. It is revealed that the studied alloy undergoes multiple steps (at least five steps) before reaching the high-temperature thermodynamic equilibrium. This is distinct from the commonly believed simple path of glass → Cu10Zr7 + CuZr2 → B2-CuZr predicted by the Cu-Zr equilibrium phase diagram. In addition to thermodynamics, we emphasize that kinetic factors play a prominent role in the phase transformation process of Cu-Zr-Al BMGs. Furthermore, isothermal crystallization kinetics analyses conducted by in-situ HEXRD and DSC indicate that the formation of the initial crystalline phase, specifically the Cu10Zr7, follows an interface-controlled quasi-polymorphic process with an increasing nucleation rate. The findings of this study may provide novel insights into the crystallization mechanism of glass-forming supercooled liquids from a thermophysical perspective.

Anionic surfactant-activated remediation of Pb, Cd, As contaminated soil by electrochemical technology

Lead (Pb), cadmium (Cd) and arsenic (As) contamination in soils show a growing environmental concern. However, owing to the significant differences in chemical characteristics, remediating heavy metal(loid)s of Pb, Cd and As is challenging. Herein, anionic surfactant-activated electrochemical approach was proposed to realize efficient immobilization of As, Cd and Pb heavy metal(loid)s from contaminated soils. In this innovative method, calcium lignosulfonate (CL) as anionic surfactant was used to activate Cd and Pb from contaminated soils into solution, afterwards anodically generated Fe (II) ions by the electrochemical process react with Pb and Cd to form precipitates. Meanwhile, owing to the strong binding capacities of Fe (II) ions, As contaminations were remediated. Moreover, via various characterizations and cyclic voltammetric method, the reaction kinetics and phase transformation process during the electrochemical process were analyzed in detail. These findings show great potential in optimizing the design of electrochemical treatment, which will be applied in remediating multi-component heavy metal(loid) polluted soils.