The production rate of industrial and agricultural waste is increasing due to population growth. Soil is the most important receiver of industrial and agricultural waste. Contaminants such as heavy metals in various waste after reception by the soil, immediately become part of the cycle that has different impacts on the environment. Geopolymer, as a chemical stabilizer has the potential to stabilize heavy metals in the soil. In this research, several geopolymers for the stabilization of heavy metals in soil were synthesized. Silicon dioxide (SiO2) and aluminosilicate (Al2SiO4) must be used to produce the geopolymers. Rice husk ash was used as the SiO2 source. Also, Iranian zeolite and sepiolite, and red clay soil were utilized as the source of Al2SiO4. The synthesized geopolymers were investigated for the adsorption of nickel and cadmium. Also, batch and column studies of using geopolymers for the chemical stabilization of heavy metals in soil were conducted. The results revealed a high adsorption capacity of the geopolymers. The zeolite, sepiolite, and red clay geopolymer-soil samples adsorbed 100% of the heavy metals (i.e., Ni and Cd) at a concentration of 100 ppm. The zeolite geopolymer adsorbent adsorbed 57% and 96% of Ni and Cd at a concentration of 1000 ppm, respectively. In general, it was concluded that the use of geopolymer compounds in soils with high heavy metal adsorption capacity could be an efficient approach to prevent groundwater resource pollution.

The effects of low molecular weight organic acids (LMWOAs) on the adsorption of quinclorac by sepiolite were investigated using laboratory batch technique. Experiments were conducted with two natural sepiolite samples with different crystal structures and chemical compositions and high-purity sepiolite. The LMWOAs used were acetic, oxalic, and citric acid. And the adsorption mechanism was characterized using X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), and Fourier transform infrared spectroscopy (FTIR). Our analysis revealed that adsorption of quinclorac on α-sepiolite and β-sepiolite was inhibited in the presence of 4 mmol L⁻¹ LMWOAs, whereas LMWOAs stimulated the adsorption of quinclorac in the high-purity sepiolite. Inhibition or stimulation varied across the different types of organic acids. The adsorption isotherms in the presence of 4 mmol L⁻¹ LMWOAs were better explained by Freundlich and linear model. The effect of organic acid concentrations (0–32 mmol L⁻¹) on the adsorption of quinclorac by the three sepiolite samples varies greatly depending on the type of organic acid and the property of sepiolite. FTIR, XRD, and XPS analyses showed that LMWOAs bound strongly to the Si–O bond structure, and Si–O-quinclorac-acetic acid (oxalic acid or citric acid) was formed on the surface of β-sepiolite. The adsorption of quinclorac by β-sepiolite was via hydrogen bond, complexation reactions, and charge transfer in the presence of LMWOAs. These results indicate that LMWOAs affect quinclorac adsorption through various interactions involving competition, electrostatic attraction, bridging action, and hydrogen bonding.

Pyrite, as one of the most abundant sulfide minerals, can be easily oxidized to generate acid mine drainage (AMD). In the present study, a new composite passivator named PropS-SH/sepiolite (PSPT) using γ-mercaptopropyltrimethoxysilane (PropS-SH) as the main passivator and natural sepiolite particles as filler was fabricated and used to suppress the oxidation of pyrite. Electrochemical tests and chemical leaching experiments were carried out to evaluate the passivation performance of PSPT coatings with different amount of sepiolite particles on pyrite oxidation. The results showed that the addition of appropriate sepiolite could significantly improve the inhibition ability of PropS-SH against pyrite oxidation. However, excessive addition of sepiolite particles weakened the inhibition ability of the PSPT coatings owing to aggregations of sepiolite. Additionally, the coating mechanism of PSPT on pyrite was also proposed based on the characterization of FTIR, XPS, and ²⁹SiNMR measurements, which indicated that sepiolite particles could be embedded in PropS-SH network through oxygen bridges, thus improving the stability of the composite coatings.