When oil is released into the oceans, spilled oil may get to the shoreline driven by wind and wave. This study comprehensively explored the effects of bentonite nanoclay on the oil behaviors in a water–sand system from both experimental and modeling perspectives. Four factors including nanoclay concentration, temperature, salinity, and pH have been studied. The increasing nanoclay concentration resulted in the decrease in remaining oil on sand. Higher temperature and salinity were associated with less residual oil on sand in the presence of nanoclay. The lower residual oil on sand with coexisting nanoclay was found to be at pH 7. The factorial analysis results indicated that the nanoclay concentration showed the most significant impact among these factors. Miscibility modeling results showed an increasing temperature was favorable to the nanoclay miscibility. Moreover, the effect of nanoclay on oil behavior was further revealed through the dynamic simulation, in which it can be seen the nanoclay could penetrate into oil droplets and promote the oil detachment from solid substrate. The results of this study can help understand the role of fine particles in the fate and transport of oil on shoreline and support the risk assessment and response planning after oil spill.

Clay is a natural substance widely existing in the environment. Nanoclays have small particle size, large surface area, and high porosity. Due to their special characteristics, nanoclays can be used in many different industrial applications. There is also an emerging trend for the use of nanoclays in environmental applications. Nanoclays can be used as adsorbents for the removal of various pollutants from water and gas. The suitability of nanoclays for certain type of application will depend on the requirement for pollution control, as well as the specifications of nanoclays. This article provided a comprehensive review of the specific characteristics of different types of nanoclays. The industrial applications of nanoclays were summarized. The environmental applications of nanoclays for water and gas emission treatment, as well as their toxicity, were discussed. The challenges and recommendations for future study were also proposed.

In this study, modification of the nanoclay montmorillonite adsorbent with diethanolamine and optimization of CO₂ adsorption operating conditions to improve the adsorption capacity were carried out experimentally. The temperature, pressure, and weight percent of diethanolamine were considered in the range of 30−70 °C, 1−9 bar, and 10−30%wt, respectively, as input variables and adsorption capacity (mg/g) and adsorption percentage were considered as the responses in the response surface methodology. The maximum adsorption capacity was obtained 219.9 mg/g for montmorillonite adsorbent without modification at temperature and pressure of 30 °C and 9 bar, respectively. In addition, the optimum temperature, pressure, and weight percent of diethanolamine were obtained 30 °C and 9 bar and 22%wt, respectively, and the adsorption capacity was calculated 281.8 mg/g for modified montmorillonite with diethanolamine. Additionally, the adsorbent behavior was investigated using isotherm, kinetic, and thermodynamic modeling of the adsorption process. The results showed that, based on the obtained values of R², Langmuir-Freundlich and Hill models have a better precision between isotherm models for the montmorillonite adsorbent without and with modification, respectively. Finally, the kinetic modeling result showed that the Elovich model is the best-proposed model for CO₂ capture data.

In this work, particles of nanoclay modified with poly(diallyldimethylammonium), PDDA, namely PDDA/PGV, were obtained and characterized by infrared spectroscopy (FTIR), thermogravimetric analysis (TGA), X-ray diffraction (XRD), surface area measurement (BET surface area), measurement of zero charge point (pHPCZ), and scanning electron microscopy with energy-dispersive spectroscopy (SEM/EDS). The PDDA/PGV particles were applied as adsorbent for the removal of gallic acid (GA) from aqueous solution. The effect of various parameters, such as solution pH, contact time, adsorbent mass, and temperature, was studied. The maximum adsorption capacity of PDDA/PGV (238.45 mg g⁻¹) was observed at pH 4 and 15 °C. The study of adsorption kinetics and isotherms revealed that the adsorption process was better fitted by pseudo-first order and Freundlich model, respectively. The obtained thermodynamic parameters indicate that the adsorption of GA is spontaneous and enthalpy-driven.

In the French West Indies, the chlordecone (organochloride pesticide) pollution is now diffuse becoming new contamination source for crops and environment (water, trophic chain). Decontamination by bioremediation and chemical degradation are still under development but the physical limitations of these approaches are generally not taken into account. These physical limitations are related to the poor physical accessibility to the pesticides in soils because of the peculiar structural properties of the contaminated clays (pore volume, transport properties, permeability, and diffusion). Some volcanic soils (andosols), which represent the half of the contaminated soils in Martinique, contain nanoclay (allophane) with a unique structure and porous properties. Andosols are characterized by pore size distribution in the mesoporous range, a high specific surface area, a large pore volume, and a fractal structure. Our hypothesis is that the clay microstructure characteristics are crucial physico-chemical factors strongly limiting the remediation of the pesticide. Our results show that allophane microstructure (small pore size, hierarchical microstructure, and tortuosity) favors accumulation of chlordecone, in andosols. Moreover, the clay microporosity limits the accessibility of microorganisms and chemical species able to decontaminate because of poor transport properties (permeability and diffusion). We model the transport properties by two approaches: (1) we use a numerical model to simulate the structure of allophane aggregates. The algorithm is based on a cluster–cluster aggregation model. From the simulated data, we derived the pore volume, specific surface area, tortuosity, permeability, and diffusion. We show that transport properties strongly decrease because of the presence of allophane. (2) The fractal approach. We characterize the fractal features (size of the fractal aggregate, fractal dimension, tortuosity inside allophane aggregates) and we calculate that transport properties decrease of several order ranges inside the clay aggregates. These poor transport properties are important parameters to explain the poor accessibility to pollutants in volcanic soils and should be taken into account by future decontamination process. We conclude that for andosols, this inaccessibility could render inefficient some of the methods proposed in the literature.

Some volcanic soils like andosols contain short-range order nanoclays (allophane) which build aggregates with a tortuous and fractal microstructure. The aim of the work was to study the influence of the microstructure and mesoporosity of the allophane aggregates on the pesticide chlordecone retention in soils. Our study shows that the allophane microstructure favors pollutants accumulation and sequestration in soils. We put forth the importance of the mesoporous microstructure of the allophane aggregates for pollutant trapping in andosols. We show that the soil contamination increases with the allophane content but also with the mesopore volume, the tortuosity, and the size of the fractal aggregate. Moreover, the pore structure of the allophane aggregates at nanoscale favors the pesticide retention. The fractal and tortuous aggregates of nanoparticles play the role of nanolabyrinths. It is suggested that chlordecone storage in allophanic soils could be the result of the low transport properties (permeability and diffusion) in the allophane aggregates. The poor accessibility to the pesticide trapped in the mesopore of allophane aggregates could explain the lower pollutant release in the environment.

This work investigates influence of different aluminosillicate nanoparticles (NPs) which are found in air in selected workplaces on the properties of the phospholipid (DPPC) monolayer at air–saline interface considered as ex vivo model of the lung surfactant (LS). The measurements were done under physiological-like conditions (deformable liquid interface at 37 °C) for NP concentrations matching the calculated lung doses after exposure in the working environment. Measured surface pressure–area (π–A) isotherms and compressibility curves demonstrated NP-induced changes in the structure and mechanical properties of the lipid monolayer. It was shown that hydrophilic nanomaterials (halloysite and bentonite) induced concentration-dependent impairment of DPPC’s ability of attaining high surface pressures on interfacial compression, suggesting a possibility of reduction of physiological function of natural LS. Hydrophobic montmorillonites affected DPPC monolayer in the opposite way; however, they significantly changed the mechanical properties of the air–liquid interface during compression. The results support the hypothesis of possible reduction or even degradation of the natural function of the lung surfactant induced by particle–phospholipid interactions after inhalation of nanoclays. Presented data do not only supplement the earlier results obtained with another LS model (animal-derived surfactant in oscillating bubble experiments) but also offer an explanation of physicochemical mechanisms responsible for detrimental effects which arise after deposition of inhaled nanomaterials on the surface of the respiratory system.