The removal of pesticide contaminants from water is a key priority in environmental remediation, and requires intensive effort; this necessitates modification of the properties of pillared clays (PILCs) such as porosity, pore-volume, surface area, and synthesis methods. The purpose of the present study was to test the ability of Al-pillared bentonite (Al-PILB), using [Al13O4(OH)24(H2O)12]7+ and [Al30O8(OH)56(H2O)24]18+ (keggin cations, Al13 and Al30) as pillars, to adsorb chlorinated pesticides from contaminated water. In order to maximize intercalation and uniformity of layer stacking, various ratios of the nitrate forms of the synthesized keggin cations were intercalated into the natural bentonite (BT). The synthesized materials (Al-PILBs) were characterized by various techniques, including X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive X-ray analysis (EDX), Fourier-transform infrared (FTIR) spectroscopy, UV-Vis spectroscopy, and N2 adsorption-desorption measurements. Increases in basal spacing, surface area, and pore volume were observed. The adsorption capacity of the Al-PILBs for 17 types of chlorinated pesticides from contaminated water was better than using the BT alone, e.g. for heptachlor epoxide, dieldrin, and endrin at natural pH, the maximum adsorptions obtained at equilibrium solution concentrations of 16, 20, and 20 μg/L, respectively, were 59.2, 59.15, and 60 μg/g, whereas corresponding values using pristine BT were 34.68, 39.45, and 38.9, respectively. The data were best described by the Freundlich adsorption model.

Structure control and quantitative evaluation of porous materials are essential for many industrial and consumer applications of clay minerals, and nanotubular halloysite (HNT) has been used extensively for such purposes; performance enhancements are still needed, however. The objective of the present study was to improve the gas-adsorption capacity of HNT by controlling the particle size and porosity. This was accomplished through acid treatment and particle-size fractionation by centrifugation. Various particle sizes were obtained and porosities ranged from macropores to mesopores. Natural halloysite nanotubes were modified by sulfuric acid in various concentrations to selectively remove the alumina composition of the tubes. X-ray diffraction and energy dispersive X-ray spectroscopy were used to verify the mineralogical and compositional changes. Surface modification by the acid treatment increased the inner space volume of the tubes and decreased the mass of the nanotubes because of the elimination of alumina. The gas adsorption capacity of both natural and modified halloysite nanotubes was measured quantitatively using N2 adsorption and the Brunauer-Emmett-Teller (BET) method, and the morphology was determined from transmission electron microscopy (TEM) images. The results showed that the modified halloysite nanotube was 7.47 times more efficient at gas adsorption than pristine halloysite. Moreover, the dealumination of the surface increased the inner space. Greatly increased porosity characteristics, including gas adsorption and macroporosity, were obtained through modification by acid treatment.

Porous materials have many applications for laser–matter interaction experiments related to inertial confinement fusion. Obtaining new knowledge about the properties of the laser-produced plasma of porous media is a challenging task. In this work, we report, for the first time to the best of our knowledge, the time-dependent measurement of the reflected light of a terawatt laser pulse from the laser-produced plasma of low-Z foam material of overcritical density. The experiments have been performed with the ABC laser, with targets constituted by foam of overcritical density and by solid media of the same chemical composition. We implemented in the MULTI-FM code a model for the light reflection to reproduce and interpret the experimental results. Using the simulations together with the experimental results, we indicate a criterion for estimating the homogenization time of the laser-produced plasma, whose measurement is challenging with direct diagnostic techniques and still not achieved.

The collapse of minerals and mineral assemblies under external stress is modelled using a master curve where the stress failure is related to the relative, effective elastic moduli which are in turn related to the porosity of the sample. While a universal description is known not to be possible, we argue that for most porous materials such as shales, silica, cement phases, hydroxyapatite, zircon and also carbonates in corals and agglomerates we can estimate the critical porosity ϕc at which small stresses will lead to the collapse of the sample. For several samples we find ϕc ~0.5 with an almost linear decay of the bulk moduli with porosity at ϕc <0.5. The second scenario involves the persistence of elasticity for porosities until almost 1 whereby the bulk modulus decreases following a power law κ ~ (1–ϕm, m>2, between ϕ = 0.5 and ϕ = 1.

Nanostructured silica materials with different morphologies and adjustable pore size have been studied by researches worldwide for several applications such as catalysis, separation, adsorption, and templates for new materials. The main interest in the development of these materials is to obtain a structure with a specific combination of pore sizes for a particular application. The morphology and textural properties of pores can be easily changed with the modification of the synthesis parameters, among these, the choice of surfactant or structure directing agent (SDA).

Accordingly, in this work, three types of nanostructured silica with different mesoporosity were synthesized by using of CTAB and Pluronic 123 as structure directing agents: SBA-15 and MCM-41 unimodal mesoporous silica and SBA-15/MCM-41 bimodal mesoporous silica.

To evaluate the effect of surfactant on the morphology and textural properties of pores, the materials were characterized by scanning electron microscopy (SEM), X-ray Diffraction (XRD) and nitrogen sorption (BET).

A novel porous material of composition Zn3(VO4)2⋅3H2O was prepared hydrothermally. The solid crystallizes in the hexagonal space group P6, with a=6.078 77(8), c=7.1827(2) Å, and V=229.857 Å3.