The zirconium metal - organic framework MIP-202(Zr), based on L-aspartic acid, was prepared by hydrothermal method and used for study of ruthenium adsorption from aqueous solutions. The obtained material was characterized by X-ray diffraction (XRD), infra red spectroscopy (IR), thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), scanning electron microscopy (SEM) and X-ray photoelectron spectroscopy (XPS). The batch adsorption experiment was performed for determination of adsorption equilibrium, kinetics and thermodynamics parameters to Ru(III) from aqueous solution on MIP-202(Zr). The data of ruthenium sorption onto MIP-202(Zr) were fitted and analyzed by the Langmuir, Freundlich and Temkin equilibrium isotherm models, while the Langumir adsorption isotherm models fit the best. Kinetic data were analyzed by four kinetic models, and ruthenium sorption on MIP202(Zr) can be describes the best by intra particle diffusion (Weber Morris). Analysis of thermodynamic properties of ruthenium ions sorption onto MIP-202(Zr) shows that the sorption process has a spontaneous and endothermic nature and is energetically beneficial.

Antibiotics, as emerging persistent pollutants, pose significant threats to human health. The effective and low-cost removal of ciprofloxacin (CIP) from wastewater has become an important research focus. In this study, fly ash (FA) was used as the raw material, and modified fly ash (MFA) was prepared by varying microwave power, alkali concentration, and immersion time to investigate its adsorption characteristics for CIP. Results showed that the optimal preparation conditions for MFA with the most effective adsorption of CIP, using the Box-Behnken response surface methodology, were a microwave power of 480 W, an alkali concentration of 1.5 mol/L, and a modification time of 3 h. Scanning electron microscopy, Fourier transform infrared spectroscopy, and X-ray diffraction analyses revealed that after modification, the glassy structure of FA is destroyed, the specific surface area is increased, and obvious hydroxyl O-H absorption peaks appear. Both FA and MFA exhibited adsorption processes for CIP that conformed to pseudo-second-order kinetics and the Langmuir equation. Maximum adsorption of CIP (9.61 and 12.67 mg/g) was achieved at pH = 6. With increasing temperature, the adsorption capacity of both FA and MFA for CIP decreased, indicating an exothermic process. The adsorption capacity of CIP decreased with increasing ion concentration, with the impact order of ions being Al3+  > Ca2+  > Na+. The results show that pore filling, electrostatic interaction, ion exchange and complexation are the main ways of CIP adsorption by FA. Microwave alkali modified fly ash is an economical and efficient adsorbent for CIP removal in water, realizing the purpose of \"treating waste with waste\". This study provides a scientific basis for controlling CIP treatment in wastewater.

The role of microplastics (MPs) as pollutant carriers and their influence on the fate of organic pollutants has received considerable attention. However, the impacts of MPs on the adsorption of amide herbicides in soil, have not been investigated. In this study, non-biodegradable (polyethylene, PEM) and biodegradable (polybutylene adipate terephthalate, PBATM) MPs were aged by exposure to one month of ultraviolet irradiation. The impacts of MPs on the adsorption of napropamide (Nap) in two agricultural soils (black soil [BS] and fluvo-aquic soil [CS]) were investigated through batch experiments. The findings suggested that the adsorption of Nap onto PEM was mainly governed by physical processes, while, chemical mechanisms, should not be overlooked on PBATM. With the addition of 0.2% MPs, the maximum adsorption capacity (Qm) and adsorption distribution coefficient (KF) of soil containing PEM (soil-PEM) were higher than that of soil-PBATM, however, the Qm and KF values of soil-PBATM for Nap were higher when the addition of MPs was 2%. After UV aging, the increased specific surface area of MPs led to an increased adhesion of soil particles. These were attributed to the different surface properties and concentrations of different (aged) MPs, resulting in differences in the inhibition effect by soil particles. The adhesion of soil particles was confirmed by X-ray photoelectron spectroscopy. Additionally, regardless of the addition of MPs, the Qm values of BS for Nap were higher than those for CS. In summary, MPs can alter the adsorption of Nap in soil, influencing both its mobility within the soil ecosystem and the environmental risk.

Using biochar for dye wastewater treatment is attracting interest due to its excellent adsorption properties and low costs. In this work, a novel biochar derived from oxytetracycline fermentation residue (functionalized OFR biochar, FOBC) was investigated as a efficient adsorbent for typical dyes removal. At 25 °C, the maximum adsorption capacity calculated by Langmuir model of FOBC-3-600 for methylene blue (MB), malachite green (MG), and methyl orange (MO) reached 643.97, 617.89, and 521.03 mg/g, respectively. The kinetics and isotherm model fitting showed that the chemisorption and physisorption both occurred during the adsorption process. Dyes were efficiently adsorbed through pore filling, electrostatic attraction, π-π interactions, and surface complexation. And the cycling experiment and environmental risk assessment indicated that the FOBC-3-600 had excellent recyclability and utilization safety. Overall, this study provides a practical method to simultaneously treat the dyeing wastewater and utilize the antibiotic fermentation residue.

Due to the serious threat posed by tebuconazole to the aquatic ecosystem, it is imperative to develop a highly efficient adsorbent material for the sustainable remediation of tebuconazole-contaminated water. Herein, a phosphorus (P)-doped biochar from corn straw and H3PO4 was fabricated by one-step pyrolysis for tebuconazole adsorption. Results showed that the P-doped biochar produced at 500℃ (PBC500) possesses a large specific surface area (SSA=869.6 m2/g), abundant surface functional groups, and the highest tebuconazole adsorption capacity (429.6 mg/g). The adsorption of tebuconazole on PBC500 followed pseudo-second-order kinetics and Langmuir adsorption isotherm models. Thermodynamic calculations indicated that the adsorption of tebuconazole by PBC500 was a spontaneous, endothermic process with a random increase. Adsorption mechanism mainly involves pore filling, π-π interactions, hydrogen bonding, and hydrophobic interaction. Moreover, PBC500 demonstrated robust anti-interference capabilities in adsorbing tebuconazole from diverse water sources and exhibited excellent reusability, underscoring its potential for a broad array of practical applications.

In addition to filtering some sediments, hydrophobic wood sponges can also absorb many organic solvents, particularly crude oil. The leakage of crude oil poses a serious threat to the marine ecosystem, and oil mixed with water also generates great danger for its use. From the perspective of low cost and high performance, wood sponges exhibit great potential for dealing with crude oil pollution. Wood sponge is a renewable material. With a highly oriented layered structure and a highly compressible three-dimensional porous frame, wood sponges are extremely hydrophobic, making them ideal for oil-water separation. Currently, the most common approach for creating wood sponge is to first destroy the wood cell wall to obtain a porous-oriented layered structure and then enhance the oil-water separation ability via superhydrophobic treatment. Wood sponge prepared using various experimental methods and different natural woods exhibits distinctive properties in regards to robustness, compressibility, fatigue resistance, and oil absorption ability. As an aerogel material, wood sponge offers multi-action (absorption, filtration) and reusable oil-water separation functions. This paper introduces the advantages of the use of wood sponge for oil-water separation. The physical and chemical properties of wood sponge and its mechanism of adsorbing crude oil are explained. The synthesis method and the properties are discussed. Finally, the use of wood sponge is summarized and prospected.

The low-grade zinc oxide ore was sulfidized to increase the efficiency of flotation, but the effect of pre-sulfidization on the adsorption mechanism of octadecyl amine (ODA) on the smithsonite surface is currently unclear. In this study, the effect of pre-sulfidization on the adsorption mechanism of ODA and the flotation behavior was studied using smithsonite and pre-sulfidized smithsonite as the samples by zeta potential, contact angle measurement, total organic carbon analyzer (TOC), quartz microcrystalline balance (QCM), Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), and micro-flotation tests. Micro-flotation tests showed that the pretreatment of sulfidization could improve the floatability of smithsonite. Zeta potential and contact angle measurements demonstrated that pre-sulfidization could favor the adsorption of ODA, which is further confirmed by the adsorption tests of ODA using TOC and QCM. Furthermore, FTIR and XPS analysis showed that pre-sulfidization changes the adsorption mode of ODA, changing it from physical adsorption to chemical adsorption. These results suggested that the favorable effect of pre-sulfidization on the adsorption of ODA and the flotation of smithsonite might provide important guidance for industrial application.

In this study, a high-Si (Si) adsorbent (APR@Sam) was prepared by acid leaching slag (APR) from lead-zinc (Pb-Zn) tailings based on high-temperature alkali melting technology. The synthesized Si-based materials were applied to aqueous solutions contaminated with Pb and cadmium (Cd) to investigate the crucial role of active Si in sequestering heavy metals. The adsorption capacities of APR@Sam and the Si-depleted material (APR@Sam-NSi) were studied under different pH and temperature conditions. The results showed that as the pH increased from 3 to 7, the adsorption capacity increased, the active Si content in the solution increased by 63 %, and the maximum pH of the solution after adsorption was 7.12. After the removal of active Si, the Pb (II) and Cd (II) adsorption capacities of APR@Sam decreased by 45 % and 11.96 %, respectively. OH- promoted the release of Si into the solution, enhancing the material\'s adsorption efficiency. The reaction mechanism is mainly attributed to surface complexation guided by Si-O and Si-O-Si bonds, metal cation exchange, and bidentate coordination. The results indicated that the Si component is critical for the removal of Pb (II) and Cd (II) by APR@Sam and provide valuable insights into resource recovery strategies from leaching residues.

During the water treatment process, chlorination and ultraviolet (UV) sterilization can modify microplastics (MPs) and alter their physicochemical properties, causing various changes between MPs and other pollutants. In this study, the impact of chlorination and UV modification on the physicochemical properties of polystyrene (PS) and polyvinyl chloride (PVC) were investigated, and the adsorption behavior of pefloxacin (PEF) before and after modification was examined. The effect of pH, ionic strength, dissolved organic matter, heavy metal ions and other water environmental conditions on adsorption behavior was revealed. The results showed that PS had a higher adsorption capacity of PEF than PVC, and the modification increased the presence of O-containing functional groups in the MPs, thereby enhancing the adsorption capacity of both materials. Chlorination had a more significant impact on the physicochemical properties of MPs compared to UV irradiation within the same time period, leading to better adsorption performance of chlorination. The optimal pH for adsorption was found to be 6, and NaCl, sodium alginate and Cu2+ would inhibit adsorption to varying degrees, among which the inhibition caused by pH was the strongest. Chlorination and UV modification would weaken the inhibitory effect of environmental factors on the adsorption of PEF by MPs. The main mechanisms of adsorption involved electrostatic interaction and hydrogen bonding. The study clarified the effects of modification on the physicochemical properties of MPs, providing reference for subsequent biotoxicity analysis and environmental protection studies.

The objective of this research was to develop and assess chitosan-grafted copolymer/HZSM5 zeolite Schiff base nanofibers for Cu2+ and Zn2+ adsorption from aqueous media. Nanofibers were prepared via electrospinning and characterized using XRD, FTIR, 1H NMR, FESEM, TGA, BET, and XPS. The study evaluated the effect of unmodified HZSM5 and Schiff base functionalization on adsorption capacities. Incorporating 10.0 wt% zeolite Schiff base as the optimum content into the chitosan-grafted copolymer significantly enhanced adsorption, achieving increases of 98.2 % for Zn2+ and 42.2 % for Cu2+. Specifically, Zn2+ adsorption increased from 27.6 to 54.7 mg/g, and Cu2+ from 67.1 to 95.4 mg/g. Factors such as temperature, pH, adsorption time, and initial cation concentration were analyzed. Kinetic studies revealed a double-exponential model, and isotherm analysis indicated a good fit with the Redlich-Peterson model, showing maximum monolayer capacities of 310.1 mg/g for Cu2+ and 97.8 mg/g for Zn2+ (pH 6.0, 240 min, 45 °C). The adsorption thermodynamics indicated a spontaneous and endothermic adsorption. Reusability tests showed minimal capacity loss (4.91 % for Cu2+ and 5.59 % for Zn2+) after five cycles. The nanofiber displayed greater selectivity for Cu2+ over Zn2+ in multi-ion systems and real electroplating wastewater, highlighting its potential for targeted heavy metal removal.