Particle Surface Potential Research Articles

Effect of the main components in gasification wastewater on the surface properties of coal water slurry

AbstractCoal water slurry is an advanced and efficient clean coal technology; using gasification wastewater to prepare coal water slurry can recycle wastewater and improve energy utilization efficiency. As the complex substances in wastewater have a great influence on the slurry properties, the effects of organic matter, metal ions, and ammonia nitrogen in gasification wastewater on the surface properties of coal water slurry are studied in this paper in order to provide new ideas for slurry mechanism of coal water slurry prepared from wastewater. Results show the following: (a) Compared with ordinary coal water slurry, the concentration of coal water slurry prepared from wastewater with high organic content increased by 2.9%, while the concentration of coal water slurry prepared from wastewater with high ammonia nitrogen content decreased by 2.1%. (b) The contact angles of coal water slurry prepared with phenols, alcohols, and urethane are reduced by 2.8°, 6.3°, and 1.5°, respectively, so organic matter can change the hydrophilicity of coal particles and affect slurryability. (c) Mg2+ and Ca2+ have basically no effect on slurry. Fe3+ reduces the absolute value of Zeta potential by 33.1, and Cu3+ increases that by 22.8, as they affect the slurryability by changing the surface potential of coal particles and the absorption of additives. (d) Ammonia nitrogen influences the slurryability by changing the pH value of the slurry. The conclusion of the influence mechanism of organic matter, metal ions, and ammonia nitrogen in wastewater on slurryability can provide a technical reference for the selection of suitable wastewater to prepare coal water slurry.

Dust particle surface potential in an argon-helium plasma using the (r,q)-distribution function

Abstract In this paper, the dust particle surface potential for argon-helium plasma is evaluated analytically and numerically in the context of negatively charged dust particles by employing a power-law r , q -distribution function. Recent studies have reported the argon-helium plasma and conducted a brief theoretical and experimental survey. To deepen our understanding further, this study aims to analyze the argon-helium plasma comprehensively using the same pattern but with the r , q -distribution function. For this purpose, the current balance equations are derived for electron, helium and argon ions, when these charge species attain the quasineutrality condition. We numerically examined the currents of plasma species for a broad range of effective distribution function parameters r and q . It is revealed that the surface potential of dust particles is significantly affected by the parameters r and q , helium ion-to-electron temperature ratio, argon ion-to-electron temperature ratio, and helium ion to argon ion number density ratio. By incorporating the multi-ion (argon-helium) species, the significance of low-temperature non-Maxwellian dusty (complex) plasma is briefly examined.

Aerosol fluidized bed coating: Exploring the impact of process conditions on process yield, coating coverage and thickness

Aerosol droplets are used to coat fluidized particles in this work. Coating experiments utilizing aerosol droplets (with a mean diameter of around 1μm) were performed under different process conditions to explore their impact on process yield, as well as on coating coverage. Core materials were glass and porous γ-Al2O3, which had mean diameters of 653μm and 610μm, respectively. Sodium benzoate (NaB) solution and silicon dioxide (SiO2) nanosuspension were used as the coating liquid. After sampling, particle pictures were taken by a scanning electron microscope and analyzed using image processing to determine the coating coverage. To simulate the coating process and determine, for each experiment, a factor for preferential deposition on already occupied positions, Monte Carlo simulations were used. Also, some particles were cut in the middle to measure coating layer thickness. Intraparticle coating thickness distribution from Monte Carlo simulations coarsely matches the measured thickness from cut particles. Results show that the process yield, coating coverage, and preference factor are affected by experimental conditions such as expanded bed height, fluidization air temperature, atomizing pressure, the number of aerosol inlets, as well as the surface potential of core particles. This study is first to examine the impact of surface charge of different core materials on droplet deposition. In an experiment with SiO2 nanosuspension, γ-Al2O3 cores could be coated quite uniformly with SiO2 nanoparticles with a layer thickness of ca. 1.1μm. This shows the potential of aerosol droplet deposition as a novel semi-wet method for coating large particles with nanoparticles without using any binders.

Development and Evaluation of a Novel Hyaluronic Acid and Chitosan-modified Phytosome for Co-delivery of Oxymatrine and Glycyrrhizin for Combination Therapy.

Multidrug resistance (MDR) of cancer cells is a major obstacle to efficient cancer chemotherapy. Combination therapy is expected to enhance the anticancer effect and reverse MDR. Numerous patents involve different kinds of nanoparticles for the co-delivery of multiple chemotherapeutics, but the FDA has approved none. In this study, oxymatrine (OMT) and glycyrrhizin (GL) were co-loaded into phytosomes as the core of nanocarriers, and the shell was cross-linked with chitosan (CS) and hyaluronic acid (HA) with the capability for the controlled, sequential release and the targeted drug uptake. Phospholipid complexes of OMT and GL (OGPs) were prepared by a solvent evaporation technique and could self-assemble in an aqueous solution to form phytosomes. CS and HA were sequentially coated on the surface of OGPs via electrostatic interactions to obtain CS coated OGPs (CS-OGPs) and HA modified CS-OGPs (HA-CS-OGPs), respectively. The particle size and zeta potential were measured to optimize the formulations. In vitro cytotoxicity and cellular uptake experiments on HepG2 cells were performed to evaluate the anticancer activity. OGPs were obtained with nano-size around 100 nm, and CS and HA coating on phytosomes could change the particle size and surface potential. The drug loading of OMT and GL showed that the nanocarriers could maintain a fixed ratio of 1:1. The in vitro release experiments indicated the release of OMT and GL was pH-dependent and sequential: the release of OMT from CS-OGPs and HA-CS-OGPs was significantly increased at pH 5.0 compared to the release at pH 7.4, while GL exhibited sustained released from CS-OGPs and HA-CS-OGPs at pH 5.0. Furthermore, in vitro cytotoxicity and cellular uptake experiments on HepG2 cells demonstrated that the co-delivery system based on phytosomes had significant synergistic anti-tumor activities, and the effects were enhanced by CS and HA modification. The delivery of OMT and GL via HA-CS-OGPs might be a promising treatment to reverse MDR in cancer therapy.

Deguelin and Paclitaxel Loaded PEG-PCL Nano-Micelles for Suppressing the Proliferation and Inducing Apoptosis of Breast Cancer Cells.

Deguelin (DGL) is a natural flavonoid reported to exhibit antitumor effects in breast cancer (BC). PEG-PCL (Polyethylene Glycol- Polycaprolactone), as polymeric micelles, has biodegradability and biocompatibility. The aim of this study was to investigate whether the nanoparticular delivery system, PEG-PCL could improve the bioavailability of DGL for suppressing proliferation of BC cells. PEG-PCL polymers were first prepared by ring-opening polymerization, and DGL and paclitaxel (PTX)-loaded PEG-PCL nano-micelles were formulated via the film dispersion method. The composition and molecular weight of PEG-PCL were analyzed by nuclear magnetic resonance and fourier Transform infrared spectroscopy (FTIR) spectra. Particle size, surface potential and hemolytic activity of micelles were assessed by dynamic light scattering, transmission electron microscopy and hemolysis assay, respectively. Then proliferation and apoptosis of MDA-MB-231 and MDA-MB-468 cells were tested with Edu staining, CCK-8, TUNEL staining, and Flow cytometer. Caspase 3 expression was also assessed by Western blot. Our results first indicated that PEG2000-PCL2000 was successfully synthesized. DGL and PTX-loaded PEG-PCL nano-micelles were rounded in shape with a particle size of 35.78 ± 0.35 nm and a surface potential of 2.84 ± 0.27 mV. The micelles had minimal hemolytic activity. Besides, we proved that DGL and PTX-loaded PEG-PCL nano-micelles could suppress proliferation and induce apoptosis in BC cells. The DGL and PTX-loaded PEG-PCL nano-micelles constructed in this study had a prominent inhibitory role on proliferation and a remarkable promotional role on apoptosis in BC cells. This study proposes that nano-micelles formed by PEG-PCL can enhance the cytotoxicity of Paclitaxel against breast cancer cells, and concurrently, the loading of Deguelin may further inhibit cell proliferation. This presents a potential for the development of a novel therapeutic strategy.

Adsorption of Polyetheramine-230 on Expansive Clay and Structure Properties Investigation.

Polyetheramine (PEA) is a swelling inhibitor used to address engineering challenges arising from the interaction between montmorillonite (Mt) and water. This study comprehensively investigates the adsorption characteristics of PEA on three representative expansive clay samples: Na-Mt, Ca-Mt, and engineered expansive soil. Additionally, the desorption of exchangeable ions is examined. The findings reveal that a two-stage adsorption kinetic model and a pseudo-second-order kinetic model can properly describe the adsorption kinetics of PEA on expansive clays. PEA exhibits a strong capacity for ion exchange with sodium ions, while the exchange capacity for calcium ions is limited. Both protonated and non-protonated PEA contribute to rapid adsorption processes. The adsorption isotherms are well-fitted by the Langmuir and Freundlich models, with the Langmuir model being reasonable. At lower equilibrium concentrations, a higher proportion of the adsorption amount is attributed to ion exchange compared to higher equilibrium concentrations. Ion exchange emerges as the primary factor contributing to the adsorption of PEA on Na-Mt, whereas the adsorption of PEA on Ca-Mt and expansive soil is primarily attributed to physical adsorption by non-protonated PEA. X-ray diffraction results reveal significant intercalation effects of PEA as they penetrate the interlayer space and hinder interlayer ion hydration. Fourier transform infrared spectrum results demonstrate that the adsorption of PEA minimally impacts the framework of Mt structural units but primarily reduces the adsorbed water content. Clay-PEA composites exhibit a decreased affinity for water. Zeta potential experiments indicate that the adsorption of PEA significantly diminishes the surface potential of clay-PEA composite particles, effectively inhibiting their hydration dispersion.

Cationic surfactant assisted electrostatic self-assembly of nitrogen-rich carbon enwrapped silicon anode: Unlocking high lithium storage performance

Nitrogen-rich carbon (N-rich-C) coating is attractive to enhance capacity, reduce resistance, and alleviate volume expansion of silicon anode in Li-ion batteries. However, the non-uniform coating of N-rich-C on silicon might restrict its optimum performance. In this study, poly(diallyldimethylammonium chloride) (PDDA) is employed as a cationic surfactant to tailor the surface potential of bare ball-milled Si particles, enabling the electrostatic self-assembly between Si particles and graphitic carbon nitride as the N-rich-C precursor. Continuous N-rich-C enwrapped ball-milled silicon (Si@N-rich-C) has been obtained after pyrolysis with a high N to C ratio of 0.65 and abundant pyridinic-N and pyrrolic-N, facilitating fast kinetic transport and accommodating more Li+ ion storage. Combined with the high capacity of Si, Li-ion cell with Si@N-rich-C electrode exhibits a high capacity of 1732 mAh g−1 after 200 cycles of charge-discharge at 400 mA g−1. At high-rate testing, Si@N-rich-C also maintains a high capacity of 1673 mAh g−1 at 1000 mA g−1. This study provides an effective approach for synthesizing high-capacity silicon anode for Li-ion batteries.

Synthesis of modified polystyrene nanoparticles and their application in fine cassiterite flotation

To solve the problem of the low flotation efficiency of fine cassiterite, we synthesised a novel high-efficiency collector comprising modified polystyrene nanoparticles (MPNs) by introducing 2-butenohydroxamic acid in emulsion polymerization. The particle size, surface potential, chemical structure and surface morphology of the collector were studied. The results showed that the collector comprised 20–100 nm cationic spherical nanoparticles with hydroxamic acid groups on the surface. The pure mineral micro-flotation experiment results revealed that fine cassiterite and calcite can be effectively separated using the MPNs as collector, which indicates the collecting capability and selectivity of MPNs for cassiterite. The selective adsorption mechanism of MPNs on the surface of cassiterite was further confirmed through Fourier transform infrared spectroscopy, zeta potential and scanning electron microscopy analysis.

In Vivo Evaluation of Self-assembled nano-Saikosaponin-a for Epilepsy Treatment.

Saikosaponin-a (SSa) exhibits antiepileptic effects. However, its poor water solubility and inability to pass through the blood-brain barrier greatly limit its clinical development and application. In this study, SSa-loaded Methoxy poly (ethylene glycol)-poly(ε-caprolactone) (MePEG-SSa-PCL) NPs were successfully prepared and characterized. Our objective was to further investigate the effect of this composite on acute seizure in mice. First, we confirmed the particle size and surface potential of the composite (51.00 ± 0.25nm and - 33.77 ± 2.04 mV, respectively). Further, we compared the effects of various MePEG-SSa-PCL doses (low, medium, and high) with those of free SSa, valproic acid (VPA - positive control), and saline only (model group) on acute seizure using three different acute epilepsy mouse models. We observed that compared with the model group, the three MePEG-SSa-PCL treatments showed significantly lowered seizure frequency in mice belonging to the maximum electroconvulsive model group. In the pentylenetetrazol and kainic acid (KA) acute epilepsy models, MePEG-SSa-PCL increased both clonic and convulsion latency periods and shortened convulsion duration more effectively than equivalent SSa-only doses. Furthermore, hematoxylin-eosin and Nissl staining revealed considerably less neuronal damage in the hippocampal CA3 area of KA mice in the SSa, VPA, and three MePEG-SSa-PCL groups relative to mice in the model group. Hippocampal gamma-aminobutyric acid-A (GABA-A) receptor and cleaved caspase-3 expression levels in KA mice were significantly higher and lower, respectively, in the three MePEG-SSa-PCL treatment groups than in the model group. Thus, MePEG-SSa-PCL exhibited a more potent antiepileptic effect than SSa in acute mouse epilepsy models and could alleviate neuronal damage in the hippocampus following epileptic seizures, possibly via GABA-A receptor expression upregulation.

Calculation of Shear Layer Thickness of Ionic Rare Earth Particles in Mixture Electrolytes during In-Situ Leaching Process

During in-situ mining and leaching of ionic rare earth ore, a chemical replacement reaction occurs between the leaching agent and rare earth ore. The thickness of the shear layer on the surface of colloidal particles is an important physical parameter. Based on the Gouy–Chapman double-layer theory and Poisson–Boltzmann equation, the relational expression for the thickness of the shear layer in the electric double layer on the particle surface under the condition of 2:2 + 3:2 mixture electrolytes (MgSO4 + RE2(SO4)3) is derived. On this basis, an indoor column leaching experiment of MgSO4 solution is conducted, and the surface Zeta potential of rare earth ore particles is measured using a Zetaprobe potential analyzer. The surface potential and the thickness of the shear layer in the leaching process with different concentrations solutions (2.5%, 3.0%, and 3.5%) are calculated. The effects of a MgSO4 solution concentration and particle surface potential on the thickness of the shear layer in the electric double layer are analyzed. It provides a theoretical basis for the study of the internal seepage of the ore body under the condition of the coexistence of multiple ions in the leaching process.

Correlation of surface potential and SERS-activity of Ag particles formed by electroless deposition on Si-based substrate

Correlation of surface potential and SERS-activity of Ag particles formed by electroless deposition on Si-based substrate

Charged colloidal SiO2 dispersions in water and chloroform: Synthesis, properties and perspectives in dyes adsorption

The paper proposes a new method for the synthesis of ultradispersed amorphous SiO2 powders in the reverse emulsions stabilized by sodium bis-(2-ethylhexyl) sulfosuccinate (AOT). Colloidal dispersions of the powders were obtained by ultrasonication in water and chloroform. The number average effective hydrodynamic diameter of particles in the sols was 90 and 200 nm, and ζ-potential was − 68 ± 3 and 52 ± 7 mV for water and chloroform, respectively. Accountable for charge formation and transformation are the AOT molecules that were adsorbed on the SiO2 surface during the synthesis in АОТ emulsions. In water, АОТ– ions serve as the potential-determining ones, while Na+ ions act as the counterions that form the diffusion part of the electrical double layer. With a decrease in the solvent polarity, Na+ ions become the potential-determining ones, and АОТ– ions – the counterions. Thus, the АОТ molecules embedded into the hybrid SiO2 @ АОТ particle during the synthesis are a certain switch key of the particle surface potential. The transformation of the surface charge in dependence on polarity of the organic solvent makes it possible to apply the synthesized powders both as the cation- and anion-exchange sorbents for the recovery of dyes from aqueous and non-aqueous media. In terms of fundamental advances, the novelty of our work consists in extending the ion-exchange sorption mechanism of ionic dyes to the media with a low dielectric constant.

Update to the Newly Developed Expression for the Stability Ratio of Colloidal Dispersions.

The colloidal stability, one of the basic and important properties of a colloidal dispersion, is commonly evaluated in terms of the stability ratio. In this study, a recently developed expression for the stability ratio is updated, by reformulating the fraction of successful collisions leading to secondary minimum coagulation. The updated formula reinterprets the statistical meaning of the fraction of successful collisions leading to primary or secondary minimum coagulation, ensuring that the total fraction of successful collisions is always less than or equals to 1. It was shown to be superior to the available expressions in accounting for the contribution of the primary and secondary minimum coagulations on the stability ratio. It can well interpret the stability of colloidal dispersions of spherical particles; moreover, it is of great potential to be applied to colloidal dispersions of plate-like particles. In addition, this formula is found to be consistent with the concept of the critical coagulation concentration and well interpret the effects of particle size, counterion valence, surface potential, and Hamaker constant on the colloidal stability.

Activating One/Two-Photon Excited Red Fluorescence on Carbon Dots: Emerging n→π Photon Transition Induced by Amino Protonation.

Due to the complicated nature of carbon dots (CDs), fluorescence mechanism of red fluorescent CDs is still unrevealed and features highly controversial. Reliable and effective strategies for manipulating the red fluorescence of CDs are urgently needed. Herein, CDs with one-photon excited (622 nm, QYs ≈ 17%) and two-photon (629 nm) excited red fluorescence are prepared by acidifying o-phenylenediamine-based reaction sediments. Systematic analysis reveals that the protonation of amino groups increases the particle surface potential, disperse the bulk sediments into nano-scale CDs. In the meanwhile, amino protonation of pyridinic nitrogen (-N=) structure inserts numerous n orbital energy levels between the π → π* transition, narrows the gap distance for photon transition, and induces red fluorescence emission on CDs. Present research reveals an effective pathway to activate CDs reaction sediments and trigger red emission, thus may open a new avenue for developing CDs with ideal optical properties and promising application prospects.

Effects of interleukin-4-modified gold nanozymes on the full-thickness skin defects in diabetic mice

Effects of interleukin-4-modified gold nanozymes on the full-thickness skin defects in diabetic mice

Enhancing Stability of High-Concentration β-Tricalcium Phosphate Suspension for Biomedical Application.

We propose a novel process to efficiently prepare highly dispersed and stable Tricalcium Phosphate (β-TCP) suspensions. TCP is coupled with a polymer to enhance its brittleness to be used as an artificial hard tissue. A high solid fraction of β-TCP is mixed with the polymer in order to improve the mechanical strength of the prepared material. The high solid fractions led to fast particle aggregation due to Van der Waals forces, and sediments appeared quickly in the suspension. As a result, we used a dispersant, dispex AA4040 (A40), to boost the surface potential and steric hindrance of particles to make a stable suspension. However, the particle size of β-TCP is too large to form a suspension, as the gravity effect is much more dominant than Brownian motion. Hence, β-TCP was subjected to wet ball milling to break the aggregated particles, and particle size was reduced to ~300 nm. Further, to decrease sedimentation velocity, cellulose nanocrystals (CNCs) are added as a thickening agent to increase the overall viscosity of suspension. Besides the viscosity enhancement, CNCs were also wrapped with A40 micelles and increase the stability of the suspension. These CNC/A40 micelles further facilitated stable suspension of β-TCP particles with an average hydration radius of 244.5 nm. Finally, β-TCP bone cement was formulated with the suspension, and the related cytotoxicity was estimated to demonstrate its applicability for hard tissue applications.

Essential Oil Composition of Aerial Part of Pluchea ovalis (Pers.) DC., Silver Nanoparticles Synthesis, and Larvicidal Activities against Fall Armyworm

In this study, essential oil of the aerial part of Pluchea ovalis (POEO) was isolated and employed for the synthesis of AgNPs (POEO-AgNPs). Then, larvicidal activities of POEO and PEO-AgNPs were evaluated against the larvae of fall armyworm (FAW), Spodoptera frugiderda (J. E. Smith); (Lepidoptera: Noctuidae). The potential medicinal values of P. ovalis and the lack of scientific reports on the applications of essential oils and nanoparticles of the plant species from the ecology of Ethiopia motivated the authors to carry out this research activity. The hydrodistillation technique was used for the isolation of POEO. Characterization of samples was done using gas chromatography/mass spectrometry (GC/MS), ultraviolet–visible spectroscopy (UV–Vis), scanning electron microscope-energy dispersive X-ray spectroscopy (SEM-EDX), Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), and zeta nanoanalyzer instruments. GC/MS analysis showed that sesquiterpenes (91.27%) are the dominant chemical constituents of POEO. The characteristic UV–Vis spectra absorption of POEO-AgNPs is observed at 428 nm. SEM imaging reveals that POEO-AgNPs have a dominantly spherical shape. A strong peak of EDX at 3.0 keV shows the existence of Ag element in POEO-AgNPs. XRD analysis determines the diffraction peaks of POEO-AgNPs at 2θ of 38.2°, 44.1°, 64.6°, and 77.8° which are indexed to (111), (200), (220), and (311), respectively. The average particle size and surface potential of POEO-AgNPs are 132 nm and −64.7 mV, respectively. POEO-AgNPs were stored at room temperature and 4 °C and showed good stability for about 6 months without aggregation or dissolution. The larvicidal activity was tested at 500, 250, and 125 µg/mL of POEO solution and 100% (full strength = 0.083 g/mL), 50%, and 25% POEO-AgNPs solution against 2nd instar larvae of S. frugiderda for 3 consecutive days. LC50 and LC90 are determined as 154.88 and 11,749.00 µg/mL for POEO and 69.18 and 1318.26% for POEO-AgNPs solutions, respectively. This finding will benefit the applications of POEO and POEO-AgNPs for a sustainable eco-friendly crop pest management method.

Influence of 2‐hydroxypropyltrimethyl ammonium chloride chitosan on sedimentation and volume change behavior of cohesive soil sediments

AbstractThe 2‐hydroxypropyltrimethyl ammonium chloride chitosan (HACC), introducing the functional quaternary ammonium group to the structure of Chitosan, has greatly broadened the application prospect. The influence on natural cohesive soil has rarely been considered. The sedimentation tests for the natural soil in HACC solutions and the HACC‐treated soils in distilled water are considered to analyze the change of sedimentation behaviors in this paper. Moreover, the potential change on the surface of soil particles, the change in particle size distribution, X‐ray diffraction of Ca‐montmorillonite/HACC, and scanning electron microscopy images are investigated to explain the reasons for the results. Results indicate that the surface potential of soil particles achieved reversal, and the particle size had significant agglomeration. The adsorption of HACC results in the rapid sedimentation of the treated soils in water. HACC has a significant influence on setting time and final volume. HACC cannot inhibit the interlayer swelling of Ca‐montmorillonite. The dehydration process can promote the aggregation effect of the treated soils. The specific effects provided an essential train of thought to solve soil problems.

Dust particle surface potential in fusion plasma with supra-thermal electrons

By solving the current balance equations, the effect of the supra-thermal electrons on the surface potential of a negatively charged dust particle in a fusion plasma is studied based on the orbital motion limited theory. A non-Maxwellian plasma is modeled by employing a q-non-extensive velocity distribution, where a decreased q-parameter (q < 1) yields increased population of supra-thermal electrons. It is found that with the decrease in the q-parameter, the surface potentials of tungsten and carbon dust particles become more negative. When the ion temperature or ion flow velocity is increased, the dust surface potential changes non-monotonically, which is first decreasing and then increasing. For a small q-parameter, the non-monotonic variation is more pronounced and the minimum value of surface potential moves toward higher values of the ion temperature or ion flow velocity. Due to the dependence of the dust particle surface potential on the supra-thermal electrons, the increased proportion of supra-thermal electrons causes the increase in the ion drag force and the decrease in the dust particle lifetime. Here, lifetime refers to the time taken for the dust surface temperature to increase from its initial value to the sublimation temperature (for carbon) or the melting temperature (for tungsten). The decrease in lifetime caused by supra-thermal electrons is significant as the dust particle radius is increased.

Investigating the Mechanical Property and Enhanced Mechanism of Modified Pisha Sandstone Geopolymer via Ion Exchange Solidification

The Yellow River has the highest sediment concentration in the world, and the Yellow River coarse sediment mainly comes from a particular kind of argillaceous sandstone, Pisha sandstone. This paper reports an investigation of the possibility of development of low-cost engineering materials using Pisha sandstone via ion exchange modification. The effect of modifiers with different concentration on the inhibition of volume expansion and the strength enhancement of modified Pisha sandstone were studied via ion exchange solidification. The effects of the concentration of ten types of modifier solutions and curing age were considered. The hydration of the mineral components, particle surface potential and reaction products were studied, respectively, by XRD, zeta potential, TG/DTG and SEM. Expansion volume and shear strength tests were conducted to assess the volume stability and mechanical property of modified Pisha sandstone. It showed that the expansion of Pisha sandstone was controlled and that the volume stability and shear strength were improved via ion exchange modification. The results of XRD, TG/DTG and SEM showed that the spacing of the crystal layers of the Pisha sandstone clay mineral and the mass lost had decreased significantly. When the concentration of the modifier was 0.05 mol/L, the volume reduced by 54.55% maximum and the shear strength reached the peak of 138 kPa.