In this study, hierarchical MgAl-LDH (layered double hydroxide) nanoparticles with a flower-like morphology were prepared under a hydrothermal condition by employing worm-like micelles formed by cetyltrimethylammonium bromide (CTAB) and salicylic acid (SA) as templates. The morphology and structure of the materials were characterized by Brunauer–Emmett–Teller (BET), SEM, and XRD analyses. The performance for the adsorption of sulfonated lignite (SL) was also investigated in detail. FTIR was used to detect the presence of active functional groups and determine whether they play important roles in adsorption. The results showed that the hierarchical MgAl-LDH nanoparticles with a specific surface area of 126.31 m²/g possessed a flower-like morphology and meso–macroporous structures. The adsorption capacity was high—its value was 1014.20 mg/g at a temperature of 298 K and an initial pH = 7, which was higher than traditional MgAl-LDH (86 mg/g). The adsorption process of sulfonated lignite followed the pseudo-second-order kinetics model and conformed to Freundlich isotherm model with a spontaneous exothermic nature. In addition, the hierarchical MgAl-LDH could be regenerated and used, and the adsorption was high after three adsorption cycles. The main adsorption mechanisms were electrostatic attraction and ion exchange between the hierarchical MgAl-LDH and sulfonated lignite.

Co-precipitation of mineral-based salts during scaling remains poorly understood and thermodynamically undefined within the water industry. This study focuses on investigating calcium carbonate and calcium sulfate mixed precipitation in scaling. Scaling is often observed in the produced water supply as a result of treatment processes. Co-precipitation results were compared with experimental results of a single salt crystallization. Several parameters were carefully monitored, including the electrical conductivity, pH value, crystal morphology and crystal form. The existence of the calcium carbonate scale in the mixed system encourages the loose calcium sulfate scale to become more tightly packed. The mixed scale was firmly adhered to the beaker, and the adhesion of the co-deposition product was located between the pure calcium sulfate scale and the pure calcium carbonate scale. The crystalline form of calcium sulfate was gypsum in both pure material deposition and mixed deposition, while the calcium carbonate scale was stable in calcite form in the pure material deposition. In the co-deposition, apart from calcite form, some calcium carbonate scale crystals had metastable vaterite form. This indicated that the presence of SO₄²⁻ ions reduced the energy barrier of the calcium carbonate scale and hindered its transformation from a vaterite form to a calcite one, and the increase in HCO₃⁻ content inhibited the formation of calcium sulfate scale.

Sludge based adsorbent (S-AB) converted by oily sludge can make full use of the precious resource. In this paper, oily sludge and discarded sawdust are used to prepare adsorbent through chemical activation. The adsorbent prepared are used to adsorb raw petroleum. Firstly, the most reasonable chemical activator ZnCl₂ is ascertained through parallel comparative experiments. The characterization results of N2-adsorption are consistent with adsorption experiment results, which shows that higher mesopore surface area and volume are benefitted to adsorption process. Secondly, the optimization of preparation technology is investigated through orthogonal experiment after parallel comparative experiments. The adsorption capacity of S-AB-ZnCl₂ is stronger when the preparation condition are as follows: activation temperature of 550 ℃，activation time of 3.5 h, solid-liquid ratio of 1:1.5, sludge-sawdust ratio of 1:0.5 and heating rate of 15 ℃/min. The maximum quantity adsorbed Q₀=434.78 mg/g, calculated through Langmuir adsorption isothermal models, of S-AB-ZnCl₂ prepared under optimized condition is bigger than that before optimization. In addition, the most reasonable kinetics fits were second-order model.

The discharge of large amounts of oily sludge heat treatment residues constitutes a severe threat to the environment. However, little is known about the toxicity of these heat-treated residues. Current research has mainly focused on the toxic effects of single heavy metals or single hydrocarbons on plants, whereas the phytotoxic effects of hydrocarbon–metal mixtures have remained largely unexplored. In this study, pot experiments were conducted to evaluate the effects of different proportions of heat treatment residues (pyrolysis, heat-washing, and high-temperature oxidation residues) from three kinds of oily sludge on the physiological and biochemical parameters of mung bean plants. Higher proportions of residues decreased the germination rates and enzyme activity of mung beans compared to uncontaminated soil. When pyrolysis residue, hot-washing residue, and high-temperature thermal oxidation residue are used in green planting soil, their content must be lower than 30%, 90%, and 70%, respectively. Additionally, our findings indicated that the accumulation level of pollutants in oily sludge heat treatment residues was not high. However, the three kinds of residues exhibited different degrees of plant toxicity. The pyrolysis residue still exhibited strong ecotoxicity, even at low concentrations. In contrast, the toxicity of the hot-washing residue was much lower than that of the pyrolysis residue and the high-temperature thermal oxidation residue. Our findings indicated that mung bean is highly tolerant of contaminated soil and is therefore well suited for phytoremediation applications.