Oil-contaminated soils resulted from drilling activities can cause significant damages to the environment, especially for living organisms. Treatment and management of these soils are the necessity for environmental protection. The present study investigates the field study of seven oil-contaminated soils treated by different stabilization/solidification (S/S) methods, and the selection of the best treated site and treatment method. In this study, first, the ratios of consumed binders to the contaminated soils (w/w) and the treatment times for each unit of treated soils were evaluated. The ratios of consumed binders to the contaminated soils were between 6 and 10% and the treatment times for each unit of treated soils were between 4.1 and 18.5 min/m³. Physicochemical characteristics of treated soils were also determined. Although S/S methods didn’t change the water content of treated soils, they increased the porosity of soils. Unexpectedly, the cement-based S/S methods didn’t increase the pH of the treated soils. The highest and the lowest leaching of petroleum hydrocarbons was belonging to S/S using diatomaceous earth (DE) and the combination of Portland cement, sodium silicate and DE (CS-DE), respectively. The best acid neutralization capacity was obtained for soils treated using the combination of Portland cement and sodium silicate (CS). Based on the best-worst multi-criteria decision-making method (BWM-MCDM), the soils treated using CS-DE was select as the best. The BWM-MCDM can be used as an effective tool for the selection of the best alternative in all areas of environmental decontamination.

The N-TiO2/g-C3N4@diatomite (NTCD) composite has been prepared through a simple impregnation method, using titanium tetrachloride as precursor and urea as nitrogen-carbon source. Then the effects of calcination temperature on structure, surface property and photocatalytic activity of the catalysts were investigated. And XRD, TEM, XPS, FTIR and UV–vis diffuse adsorption spectroscopy were used to characterize the obtained powders. The photocatalytic activity of the NTCD was evaluated through the reduction of aqueous Cr (VI) under visible light irradiation (λ > 400 nm). The results demonstrated that the nano-TiO2 particles ranging from 15 to 30 nm in the crystal of anatase are well deposited on the surface of diatomite in the NTCD-500 which calcined at 500 °C for 2 h. Furthermore, the g-C3N4 with the lay thickness of 0.92 nm was attached to the surface of nano-TiO2. The N-doped TiO2 and g-C3N4 doped catalysts could co-enhance response in the visible light region and reduce band gap of NTCD-500 (Eg = 3.07 eV). And the NTCD-500 sample exhibited nearly 100% removal rate within 5 h for photocatalytic reduction of Cr (VI) which was higher activity than P25, crude TiO2@diatomite and g-C3N4@diatomite.

Three types of diatomite-based adsorbents—diatomaceous earth (DE), purified diatomite (PD), and diatomite@MgO/CaO (D@MgO) were used for adsorption decontamination of ammonium from Lake Qarun water (28.7 mg/L). The adsorption properties of the three diatomite-based adsorbents were evaluated by both batch and fixed-bed column adsorption studies. The kinetic results demonstrated removal percentages of 97.2%, 69.5%, and 100% using DE, PD, and D@MgO, respectively, at a 1 g/L adsorbent dosage. The adsorption results using DE and D@MgO showed the best fitness with pseudo-first-order kinetic and Langmuir isotherm models, while the obtained results using PD demonstrate better fitness with the Freunlidich model. The recognised fitting results with the pseudo-first-order model and estimated adsorption energies demonstrated physical uptake of ammonium by DE (5.93 kJ/mol), PD (4.05 kJ/mol), and D@MgO (7.81 kJ/mol). The theoretical maximum ammonium uptake capacity of DE, PD, and D@MgO were 63.16 mg/g, 59.5 mg/g, and 78.3 mg/g, respectively. Using synthetic adsorbents in a fixed-bed column system for treating ammonium ions in Lake Qarun water resulted in removal percentages of 57.4%, 53.3%, and 62.6% using a DE bed, PD bed, and D@MgO bed, respectively, after treating approximately 7.2 L of Lake Qarun water using a bed thickness of 3 cm, a flow rate of 5 mL/min, pH 8, and the determined ammonium concentration in Lake Qarun water (28.7 mg/L). The curves demonstrated breakthrough times of 900 min, 900 min, and 960 min for the DE bed, PD bed, and D@MgO bed, respectively, with 1440 min as the saturation time. The columns’ performances also were studied based on the Thomas model, the Adams-Bohart model, and the Yoon-Nelson model.

Sulfur-containing wastewater is very common as an industrial waste, yet a high-efficiency composite microbial agent for sulfur-containing wastewater treatment is still lacking. In this work, three novel and efficient desulfurizing bacteria were isolated from the sewage treatment tank of Zhejiang Satellite Energy Co., Ltd. They were identified as Brucella melitensis (S1), Ochrobactrum oryzae (S8), and Achromobacter xylosoxidans (S9). These three strains of bacteria were responsible for the oxidative metabolism of sodium sulfide via a similar polythionate pathway, which could be expressed as follows: S²⁻→S₂O₃²⁻/S⁰→SO₃²⁻→SO₄²⁻. Activated carbon, wheat bran, and diatomite at 1:1:1 ratio are used as carriers to construct a composite microbial agent containing the three bacteria. The desulfurization efficiency of 95% was predicted by response surface methodology under the following optimum conditions: the dosage of the inoculum was 3 g/L, pH 7.86, and temperature of 39 °C. Additionally, the impact resistance was studied in the anaerobic sequencing batch reactor. The removal capacity of microbial agent reached 98%. High-throughput analysis showed that composite microbial agent increased bacterial evenness and diversity, and the relative abundance of Brucellaceae increased from 5.04 to 8.79% in the reactor. In the process of industrial wastewater transformation, the transformation rate of sulfide by composite microbial agent was maintained between 70 and 81%. The composite microbial agent had potential for the treatment of sulfur-containing wastewater.

In this study, diatomite coated with Fe-Mn oxides (DFMO) was synthesized through calcination. The adsorption of antimonate (Sb(V)) by DFMO was studied, and environmental factors affecting the adsorption were investigated. The components of DFMO were identified as γ-Fe₂O₃, γ-MnO₂, and SiO₂, in the presence of diatomite covered with nanoscale metal oxides. Batch experiments were carried out to evaluate the antimonate adsorption performance in aqueous solution. Results showed that maximum Sb(V) adsorption capacity of DFMO reached 10.7 mg/g at pH 4, corresponding to 22.2 mg/g per unit metal oxides. Antimonate adsorption occurred on heterogenous surface, following the Freundlich and Pseudo-second order model. Overall, antimonate adsorption was favored at acidic condition due to low point of zero charge. However, when treating electroplating wastewater, neutral pH condition exhibited a higher efficiency than acidic pH, because co-existing ions in electroplating wastewater significantly affects antimony adsorption. Further investigation showed that among different potential co-existing ions, fluoride can strongly inhibit the adsorption of antimonate at 5 mg/L under pH 4. Density functional theory (DFT) analysis confirmed that adsorption energy on DFMO follows: HF < F⁻ < Sb(OH)₆⁻, indicating that fluoride is easier to bind with DFMO compared to antimonate, especially under pH 3.5 at which fluoride exists as HF. Moreover, the competitive adsorption of fluoride toward antimonate indicated the necessity of pre-treatment like neutralization and precipitation before adsorption process.

In the present study, we evaluated the insecticidal efficacy of diatomaceous earth (DE) and pirimiphos-methyl for the control of phosphine-susceptible and phosphine-resistant populations of Tribolium castaneum (Herbst) and Sitophilus oryzae (L.). Insecticides were applied on wheat or rice at two doses: DE was applied at 1000 and 2000 ppm and pirimiphos-methyl at 1 and 5 ppm. Adult mortality was measured after 7, 14, and 21 days of exposure, and progeny production capacity on the treated substrates was evaluated 65 days later. For T. castaneum, we found that DE, at 2000 ppm, was able to provide 100% control of two of the three populations tested, while for the third population mortality reached only 84%. Similarly, there were differences in mortality levels after exposure to DE-treated grains between the two S. oryzae populations tested. At 1 ppm, pirimiphos-methyl was not effective for any of the T. castaneum populations tested, but complete mortality was recorded for all populations at 5 ppm. In general, populations of S. oryzae were more susceptible than those of T. castaneum, for both commodities. Our data indicate that both insecticides can be used with success in phosphine resistance management programs, but there are populations of a given species that may be less susceptible, which constitutes a preliminary screening essential.

Diatomite (D) as a low-cost and eco-friendly clay was modified by ethylene diamine (EDA)-trimesoyl chloride (TMC) polymer to achieve a novel adsorbent for efficient removal of rhodamine B dye (RB) from wastewater samples. The EDA-TMC polymer was grafted to the surface of diatomite by in situ interfacial polymerization. The prepared p(EDA-TMC)/D adsorbent was characterized by XRD, FTIR, and SEM/EDX techniques. The effective experimental parameters on the adsorption performance were optimized with factorial design analysis. The equilibrium data were better correlated by non-linear Langmuir model compared to non-linear Freundlich model. The Langmuir monolayer adsorption capacity of the p(EDA-TMC)/D adsorbent was determined as 371.8 mg g⁻¹. The key adsorption parameters were optimized by experimental design analysis. The kinetic findings showed the adsorption mechanism of RB onto p(EDA-TMC)/D adsorbent was well designated by the pseudo-second-order kinetic model. The thermodynamic results indicate that the RB adsorption had an exothermic character in thermal nature and was less favorable with increasing temperature from 20 to 60 °C. Furthermore, the adsorption/desorption yield of p(EDA-TMC)/D was still 80%/70% after 5ᵗʰ cycle and reduced to 60%/52% at the end of 8ᵗʰ cycle. Thus, the present study revealed that the developed p(EDA-TMC)/D composite had great adsorption potential for removal of RB from wastewater samples compared to that of different kinds of adsorbents reported in the literature.

The insecticidal activity of the Diatomaceous Earth (DE) of Sig was assessed against the Dermestes haemorrhoidalis, which is the main pest affecting wheat stored in Blida, a central region of Algeria and one of the four cereal regions managed by the Algerian Inter-branch Cereals Office (AICO). The formulation was tested at two different doses: 500 and 1000 ppm against adults of the species. The bioassays were carried out in 1-litre glass jars containing soft wheat with an average moisture content of 60% mixed with diatomaceous earth and maintained at 27°C and 70% of humidity. The effectiveness of the treatment was assessed by recording adult mortality after 2, 7 and 14 days. Sig’s diatomite showed significant insecticidal activity against Dermestes haemorrhoidalis after only two days of treatment with both doses 500 and 1000 ppm. After 14 days, average mortality was more than 95% even at 500 ppm. Furthermore, electron microscopy of the diatomite particle from Sig (Algeria) reveals the architecture of the frustule. It shows a porous and brittle siliceous shell made largely of diatomite “skeletons”. This research work allowed getting insights into the mechanism of action of diatomite on the Dermestes haemorrhoidalis. On the other hand, the identification of diatomite of Sig was performed by X-ray diffraction and infrared.

A waste–struvite/diatomite compound (MAP@Dia) recovered from nutrient-rich wastewater treated by MgO-modified diatomite (MgO@Dia) was provided to immobilize lead in aqueous solution and contaminated soil. The mechanism and effectiveness of lead immobilization was investigated, and the pHₛₜₐₜ leaching test and fixed-bed column experiments were carried out to assess the risk of MAP@Dia reuse for lead immobilization. The results showed that MAP@Dia were effective in immobilizing lead in aqueous solution with adsorption capacity of 832.47–946.50 mg/g. The main mechanism of Pb immobilization by MAP@Dia could be contributed by surface complexation and dissolution of struvite followed by precipitation of hydroxypyromorphite Pb₁₀(PO₄)₆(OH)₂. Lead(II) concentration reduced from 269.61 to 78.26 mg/kg, and residual lead(II) increased to 53.14% in contaminated soil when the MAP@Dia application rate was 5%. The increased neutralization capacity (ANC) and lower lead extraction yields in pHₛₜₐₜ leaching test in amended soil suggested 5 times of buffering capacity against potential acidic stresses and delayed triggering of “chemical time bombs.” The results of column studies demonstrated that amendment with MAP@Dia could reduce the risk of lead and phosphorus (P) leaching. This study revealed that MAP@Dia could provide an effective solution for both P recycling and lead immobilization in contaminated soil.

The contamination of drinking water with arsenic has been a problem in a lot of countries around the world because of its toxicological and carcinogenic effects on human health. Porous materials modified with Fe₃O₄ nanoparticles (Fe₃O₄ NPs) represent convenient removers for that contaminant. A co-precipitation method of Fe(III) and Fe(II) in alkaline media was applied to obtain Fe₃O₄ NPs. In a first stage, single nanoparticles were synthesized and stabilized with carboxylic acids. A characterization with attenuated total reflectance Fourier transform infrared spectroscopy (ATR-FTIR), Raman spectroscopy, and X-ray diffraction (XRD) confirms a magnetite-type structure. Moreover, transmission electron microscopy (TEM) and calculations from XRD data using Scherrer’s equation indicate an average particle size of 13 nm and an average crystallite size of 10 nm, both independent of the stabilizer used. Then, the co-precipitation method studied was applied to modify kaolin, bentonite, diatomite, and silica and thus prepare magnetic composites having support-magnetite weight ratios of 2:1. Among them, silica-modified material presented the best hydraulic characteristics, an important aspect for large-scale applications such as removal under gravity. This composite has the capacity to remove up to 80 and 70% for initial concentrations of 25 and 50 μg/L, respectively, representing a convenient remover for processes developed in subsequent stages or in continuous flow.