Removal Mechanism Research Articles

Enhanced Piezocatalytic Water Splitting by Platinum‐Decorated Barium Titanate

AbstractPiezocatalysis has emerged as a promising field of research that uses mechanical energy to drive a chemical change. There is growing evidence that piezocatalysts can perform challenging chemical conversions from organic transformations to water splitting. A key challenge to piezocatlaysis is mitigating the inherent high relative permittivity of a ferroelectric material. This high permittivity restricts the transfer of carriers required for a chemical reaction to occur and reduces the reaction rate. Here the concept of producing a co‐catalyst system is taken to enhance carrier mobility increasing the observed reaction rate. The study highlights the importance of determining the sonochemical and piezocatalytic contributions to catalysis. The combination of a Pt metal co‐catalyst with BaTiO3 through a simple solid‐state method led to a four fold increase in the rate of H2 production compared to BaTiO3 and sonochemical reactions in the absence of a catalyst. BaTiO3/Pt is found to exhibit stable piezocatalytic performance over 12 h. Where there is a deviation from steady‐state water splitting, it is shown that this is due to mechanical removal of Pt rather than a phase change in the catalyst system. This work confirms the additive benefits of hybrid materials for improving piezocatalytic processes.

Activating colloidal synthesized Au catalyst by the electrochemical strategy: Gas atmosphere, electrolyte and electrochemical technique

Organic ligands are necessarily used to stabilize nanoparticles (NPs) in colloid synthesis, and the presence of these ligands in most cases can have adverse effects on heterogeneous nanocatalysis. Therefore, it is crucial to develop efficient methods to remove ligands and study the removal mechanism. In this article, we developed a combined electrochemical method (chronoamperometry (CA) + cyclic voltammetry (CV)), which can completely and efficiently remove thiol ligand from Au NPs to produce cleaned Au/C catalyst. Using the oxygen reduction reaction (ORR) activity as the evaluation criterion for ligand removal, we found that gas atmosphere (O2) plays an important role in the removal process, while the acidity and alkalinity of electrolyte have no effect on the removal efficiency. A proposed thiol ligand removal mechanism along with Au degradation is presented. The results of CA activation at an oxidation constant potential (1.7 V) indicate that oxidation of thiol alone cannot remove thiol ligand. Only if a reduction constant potential of 0.2 V is further applied, the ORR activity of Au/C catalyst will increase, indicating that both the oxidation and reduction processes of Au NPs are crucial for ligand removal. Although the CA method (with an upper potential of 1.7 V and a lower potential of 0.2 V) can efficiently remove the majority of thiol ligand, complete removal of thiol ligand requires further CV activation. Based on the relevant results, a combined electrochemical method (CA + CV) is established. Developing standardized methods for removing ligands on the surface of catalysts is important for obtaining efficient catalysts and is also important for the reproducibility of catalytic results.

Synergistic phosphorus removal mechanism of Tetrasphaera enrichment in a micro-pressure swirl reactor

To investigate the effect of Tetrasphaera’s enrichment on phosphorus removal mechanism, three micro-pressure swirl reactor (MPSR) groups were used to experiment on sewage treatment under different SRT (17.2, 50.8, and 68.2 d). Results showed that Tetrasphaera enrichment in the MPSR system was promoted by extending the SRT. After extending the SRT from 17.2 to 68.2 d, the relative abundance of Tetrasphaera increased from 3.1% to 12.1%, and the TP removal efficiency maintained above 92%. The internal circulation results indicated that after extending the SRT, glycogen and polyhydroxybutyrate were co-synthesized during the anaerobic stage, which enhanced the driving force of nutrient removal. Analysis of the microbial composition and functional gene prediction indicated that efficient phosphorus removal can be attributed to the enrichment of Tetrasphaera at long SRT. Overall, the synergistic mechanisms of Tetrasphaera in the organic matter degradation and phosphorus removal processes were integrated into the MPSR.

COF-derived porous nitrogen-doped carbon for removal of emerging organic contaminants and efficient uranium extraction from seawater

The development of adsorbents for efficient and highly selective seawater extraction of uranium was instrumental in fostering sustainable progress in energy and addressing the prevailing energy crisis. However, the complex background composition of the marine environment, including radionuclides, organic pollutants, and a large number of co-existing heavy metal ions, were non-negligible obstacles to the extraction of uranium from seawater. The present investigation successfully employed a self-templated approach to synthesize porous nitrogen-doped carbon (PNC) derived from COF, which exhibited tremendous potential as an adsorbent for pollutant removal in environmental treatment. LZU1@PNC not only retained the structural features of the original COF-LZU1, but also overcame the acid-base instability problem commonly found in COFs. Subsequently, the removal process of two typical water pollutants on the material was investigated using 2,4-DCP and [UO2(CO3)3]4-. The results demonstrated that LZU1@PNC exhibited superior removal performance for the target pollutants compared to COF-LZU1, owing to its larger specific surface area and abundant defect structure. After six desorption-regeneration cycles, LZU1@PNC still maintained a high removal rate of the target contaminants, demonstrating the stability of this material and its excellent recyclability. In addition, based on various characterization techniques, the removal mechanism of 2,4-DCP was presumed to be mainly electrostatic attraction, hydrogen bonding, and π-π stacking interactions. Conversely, the elimination process of [UO2(CO3)3]4- predominantly relied on surface complexation phenomena. The present investigation provided new perspectives and stimulated a broader study of other COF-derived carbon materials and their modifications as adsorbents for uranium extraction from seawater and other applications.

Nanofluid minimum quantity lubrication assisted grinding force model considering anisotropy of SiCf/SiC ceramic matrix composites

SiCf/SiC ceramic matrix composites with excellent thermal stability, light weight and oxidation resistance have become key components in advanced aircraft engines. Nanofluid minimal quantity lubrication (NMQL) exhibits significant potential in enhancing heat transfer and lubrication efficiency during the grinding process. The technological challenge lies in thoroughly investigating the theoretical variation rule of grinding force, assisted by nanofluid minimal quantity lubrication, and subsequently achieving low-damage machining of SiCf/SiC composites. In this study, a prediction model for the grinding force during NMQL-assisted grinding was established, integrating diverse lubrication methods, grinding wheel geometric parameters, wear degree, process parameters, the anisotropy and damage degree of SiCf/SiC composites. The model was subsequently experimentally validated through grinding tests conducted on SiCf/SiC composites under various conditions, including dry grinding (DG), flood grinding (FG), minimum quantity lubrication (MQL), and carbon nanotube nanofluids (NMQL-CNTs), across multiple grinding depths. The present investigation’s grinding force forecasting model is evidenced to possess high accuracy of precision, showcasing mean deviations of 6.64 % and 11.97 % in the perpendicular (Fn) and tangential (Ft) grinding force components, respectively. Additionally, employing NMQL-CNTs facilitates the achievement of minimal grinding force and surface finish quality. At depths of 0.4 mm and 0.6 mm during grinding, the mean Fn magnitudes under the NMQL-CNTs lubrication approach underwent a decrease of 66.7 % and 74.5 %, respectively, in contrast, the mean Ft magnitudes experienced a reduction of 55 % and 67.2 %, correspondingly, in comparison to the DG lubrication technique. Notwithstanding the consistency in the material’s brittle removal mechanism across varying lubrication strategies, the NMQL-CNTs approach effectively alleviates fiber abrasion. Concisely, the research presented herein provides foundational theoretical insights and practical technological assistance for the achievement of low damage SiCf/SiC composite processing.

Removal of enrofloxacin as well as nutrients in mariculture water by Sesuvium portulacastrum system: Insights for biodegradation, ecotoxicity of enrofloxacin

Antibiotic contamination and eutrophication in mariculture have become problems that cannot be ignored, and enrofloxacin (ENR), as an example, is especially widely used in mariculture. This study firstly revealed that Sesuvium portulacastrum, a plant with world-wide distribution in coastal zones, with its rhizosphere microorganisms, could remove ENR as well as nutrients. The S. portulacastrum system could degrade ENR to small-molecule products 1,2,3,4-tetrahydroquinolin-4-ol and (2,4-dihydroxyphenyl)-cyclopropylamine. And there were 81.3–39.2 % removals of ENR with 0.01-100 mg/L. Although ENR significantly influenced functions of rhizosphere microbial community, like decreasing nitrogen fixation, shifting trophic strategies from phototrophy to chemoheterotrophy, nutrients (NH4+-N, NO2−-N, NO3−-N and total dissolved phosphorus) removal of S. portulacastrum system was essentially unaffected at low ENR concentration (< 1 mg/L). The removal mechanism of S. portulacastrum system was explored. Neither of the isolated root exudates and rhizosphere bacteria could degrade ENR, however, without rhizosphere bacteria, ENR removal rate would decrease. Root proteins including oxidase, decarboxylase, dehydrogenase, such as laccase, isocitrate dehydrogenase, delta-1-pyrroline-5-carboxylate dehydrogenase were overexpressed. Additionally, endocytosis is a pathway for antibiotics to enter S. portulacastrum. This study demonstrated that S. portulacastrum system could be used for remediation of antibiotics-nutrients combined pollution, and deepened understanding the antibiotic removal mechanism of macrophytes in mariculture, moreover, provided new macroplant species and a theoretical basis for antibiotics removal in aquatic systems.

Statistical physics insights in the Allura Red adsorption on chitosan: Effects of adsorbents features, and experimental conditions

This study presents an innovative approach using statistical physical modeling to analyze the effect of experimental conditions and adsorbent features on removing Allura Red dye by chitosan. Five models based on statistical physics were employed to understand the removal mechanism under different experimental conditions, including variations in pH, particle sizes, chitosan deacetylation degrees, and temperatures. The best models were determined through rigorous statistical analysis and a detailed evaluation of the estimated parameters, considering their physical meaning and standard deviations. The models demonstrated high predictive capacity (coefficients of determination greater than 0.9 and low mean squared error values < 110). Analysis of the effects of experimental conditions revealed that a pH of 6.6, particles smaller than 0.10 mm, a high degree of deacetylation (84 %), and temperatures of 298 K and 308 K present the greatest potential for dye removal by chitosan. Furthermore, it was observed that, in general, the dye removal mechanism involves the formation of a double layer with two adsorption energies under the best experimental conditions, and the process occurs predominantly by physical forces (adsorption energy below 35 kJ/mol). This work contributes significantly to understanding how experimental conditions influence the mechanism of dye adsorption by chitosan, offering valuable and new insights for future applications and optimizations in the treatment of effluent-containing dyes.

Tasar silk fiber waste reinforced polylactic acid composite: Physical, mechanical, and sliding wear characterization

Incorporating natural industrial waste as a reinforcement for the development of sustainable composite is now being extensively practiced to eliminate harmful synthetic fiber. This study exhaustively evaluated the potential of tasar silk fiber waste (TSFW) as a reinforcing agent in a polylactic acid (PLA) matrix to optimize the physical, mechanical, and wear properties. Therefore, PLA-based biocomposites with varying TSFW proportions (0, 2, 4, 6, 8, and 10 by weight) are manufactured and then evaluated for physical (density, voids, water absorption), mechanical (tensile, flexural, impact, and hardness), and sliding wear properties. Results suggested that water uptake of PLA composites increases with the addition of TSFW and becomes saturated after nine days of immersion. The TSFW reinforcement at 8 wt% in PLA yields 32 % and 22 % improvement in tensile strength (66.2 MPa) and flexural strength (103.2 MPa), respectively. A remarkable improvement was observed in the impact strength at similar reinforcement (8 wt%) of TSFW with the observed value of 27.90 kJ/m2. A continuous increase in hardness was obtained by including TSFW in PLA, with the highest value of 86 Shore D recorded for 10 wt% TSFW added biocomposite. The specific wear rate of all samples increased, but the incorporation of TSFW significantly reduced the same. Microscopic examination suggests that microploughing, microcutting and groove formations were the main mechanism of material removal. After examining the results, it is recommended that TSFW be used in bidirectional mat form for further enhancement of mechanical properties and improved bonding between fiber and matrix.

Surface roughness and fracture cracks of Al2O3/TiO2 composite coating by wet chemical mechanical grinding with structured abrasives pad

In the fields of wind power, and other industries, the Al2O3/TiO2 coating is prepared and ground on the bearing ring, in order to obtain the insulation resisting the electrical erosion for the motors at high voltage. A novel wet chemical mechanical grinding (WCMG) method is proposed to finish this hard-brittle composite material, utilizing the structured diamond abrasives pad and the NaOH solution. The softened workpiece's surface under the chemical reaction was demonstrated by means of Raman spectrum, indentation and scratching tests. The analytical model of surface roughness and fracture cracks is established based on the synthesis of geometry and kinematics, contact mechanics, material removal and indentation fracture mechanics. The surface roughness of coating was reduced from initial Sa 3.293 μm down to final Sa 0.049 μm in the WCMG process with grain size 3 μm and pH 12.01, mostly attributed to the ductile removal of chemically softened coating surface.

Stamping cleaning conception on cross-contamination free multi-ceramic bioglass-tricalcium phosphate core-shell structure fabrication

Multi-ceramic additive manufacturing has always been a topic of discussion, considering that implementing multiple materials in one structure can bring innovative functionalities to it. However, the realization of the fabrication system is still plagued by cross-contamination when alternating materials. Therefore, we developed a new machine and suggested a stamping cross-contamination prevention system to address this issue. The contaminant removal mechanism was understood, efficiency was improved, and the stamping process parameters were optimized. To demonstrate, a bone hierarchical structure naturally modeled with advanced functionality to withstand mechanical loads and assist metabolic reactions was replicated. The material combination chosen included chemically identical calcium phosphates and bioglass. First, specific properties such as compressive strength were measured, and in-vitro bioactivity was evaluated to assign appropriate roles. Subsequently, the functionality of the hierarchical structure was controlled and fabricated using the previously optimized parameters. Finally, cross-contamination and multi-functionality of the generated structure were confirmed again for conclusion.

Effective removal of Cr(VI) from water by ball milling sulfur-modified micron zero-valent iron：Influencing factors and removal mechanism

To address the issues of ZVI's susceptibility to oxidation and aggregation, ball milling and Na2S·9H2O modification were employed on ZVI to enhance its efficiency in removing Cr(VI) from effluent. The characterization results expressed that S-mZVIbm had mesoporous and macroporous structures, enabling successful capture of Cr(VI). Moreover, S-mZVIbm had the highest adsorption capacity for Cr(VI) (350.04 mg/g) at pH = 2.00 and reached kinetic equilibrium within 420 min. Furthermore, the adsorption of Cr(VI) by S-mZVIbm conformed to the Avrami-fractional-order model, demonstrated that the adsorption process indicated a complex multi-adsorption process. Meanwhile, the adsorption also fit to Langmuir and Sips models, suggesting monolayer-level adsorption with heterogeneous sites located on S-mZVIbm. The S-mZVIbm could enhance Cr(VI) adsorption through various synergistic mechanisms, such as electrostatic interaction, chemical precipitation, surface complexation, and reduction. Overall, this research presented an innovative perspective for the modification of ZVI, and S-mZVIbm could be widely applied in the practical remediation of wastewater containing Cr(VI).

Tetracycline removal by immobilized indigenous bacterial consortium using biochar and biomass: Removal performance and mechanisms

The significant influx of antibiotics into the environment represents ecological risks and threatens human health. Microbial degradation stands as a highly effective method for reducing antibiotic pollution. This study explored the potential of immobilized microbial consortia to efficiently degrade tetracycline. Concurrently, the suitability of different immobilization materials were assessed, with reed charcoal-immobilized consortia exhibiting the highest efficiency in removing tetracycline (92%). Similarly, wheat-bran-loaded bacterial consortia displayed a remarkable 11.43-fold increase in tetracycline removal compared with free consortia. Moreover, adding the carriers increased the nutrients, while the activities of both intracellular and extracellular catalases increased significantly post-immobilization, thus highlighting this enzyme’s crucial role in tetracycline degradation. Finally, analysis of the microbial communities revealed the prevalence of Achromobacter and Parapedobacter, signifying their potential as key degraders. Overall, the immobilized consortia not only hold promise for application in the bioremediation of tetracycline-contaminated environment but also provide theoretical underpinnings for environmental remediation by microorganisms.

Efficient chromium remediation using eco-innovative biochar in a novel two-stage upflow fixed bed system

Chromium (Cr) pollution poses a significant environmental threat. This study addresses the highly toxic hexavalent form of chromium [Cr(VI)] by developing an innovative two-stage upflow fixed-bed system. The system uses nano iron sulfide-modified biochar (nFeS-BC), derived from spent substrates of Lentinus edodes, as the primary adsorbent. The study determines the removal mechanisms by nFeS-BC, including ion exchange, functional group interaction, complexation and co-precipitation. Fixed bed experimental results demonstrated a maximum adsorption capacity (qe) of 2.751 mg·g−1 for Cr(VI) with an initial concentration (C0) of 20 mg·g−1, bed height (Z) of 10 cm, flow rate (Q) of 2 mL·min−1, and at pH 2. The adsorption process closely followed the Thomas and Yoon-Nelson models, confirming a high fitting accuracy (R2 = 0.997), which underscores the predictability and stability of nFeS-BC in dynamic flow conditions. Subsequent treatment in a second fixed bed, filled with cetyltrimethyl ammonium bromide-modified biochar (CTAB-BC), reduced the total Cr concentration to 0 mg·L−1. Furthermore, nFeS-BC retained 50 % of its initial adsorption capacity after five regeneration cycles. This study highlights the potential of nFeS-BC within a novel fixed-bed design for efficient and sustainable treatment of actual wastewater.

A deterministic mechanism for efficient removal of arsenic and lead from wastewater using rapidly synthesized TiO2-(α-Fe2O3) nanoshells

Removal of heavy metals from wastewater using efficient techniques became demanding wherein various nanomaterials with tailored physicochemical traits can be useful. Thus, PLAL approach at an optimum laser energy was used to make TiO2-(α-Fe2O3) nanoshells (TFNSs) by mixing nanoparticles (NPs) suspension of TiO2NPs (TNPs) and α-Fe2O3NPs (FNPs) at 50 to 50 ratio. The produced nanocomposites were customized by targeting Ti that was submerged in deionized water as growth medium and then irradiate using the laser pulses with an optimum laser energy 10.6 J/cm2, spot focused size of 1.2 ± 0.2 mm, frequency of 6 Hz, and laser beam with a pulse duration of 8 ns for 15 minutes. In the course of the ablation process, the solution was agitated to achieve the formation of TNPs, FNPs, and TFNSs by preventing the formation of craters on the target surface. The obtained NSs were characterized to evaluate their structural, morphological, optical absorption and fluorescence characteristics. TEM micrographs of the liquid suspension confirmed the existence of spherical nanocrystallites of TiO2-(α-Fe2O3)NSs with mean diameter ≈12.4 ± 1.31 nm. XRD and FTIR results have been used to identify the samples crystalline nature and high purity. LSPR absorption bands of TFNSs were evidenced at 230 to 300 nm. These NSs showed prominent fluorescence peaks escorted with blue shift. Arsenic and lead removal efficiency of TFNSs from wastewater was better (over 99% at pH = 9) than TNPs and FNPs. The removal of arsenic and lead from wastewater by TNPs, FNPs and TFNSs were explained using a possible mechanism. The obtained results suggest that the proposed NSs can be potential for wastewater treatment, contributing towards sustainable growth.

Nitrogen removal capability and mechanism of a novel low-temperature-tolerant simultaneous nitrification-denitrification bacterium Acinetobacter kyonggiensis AKD4.

A low-temperature-tolerant simultaneous nitrification-denitrification bacterial strain of Acinetobacter kyonggiensis (AKD4) was identified. It showed high efficiency in total nitrogen (TN) removal (92.45% at 10°C and 87.51% at 30°C), indicating its excellent low-temperature tolerance. Transcriptomic analysis revealed possible metabolic mechanisms under low-temperature stress. Genes involved in cell growth, including ATP synthase (atpADGH), amino acid (glyA, dctA, and ilvE), and TCA cycle metabolism (gltA, fumC, and mdh) were remarkably upregulated from 1.05-3.44-fold at 10°C, suggesting that their actions enhance survivability at low temperatures. The expression levels of genes associated with nitrogen assimilation (glnAE, gltBD, and gdhA), nitrogen metabolism regulation (ntrC, glnB, and glnD), and denitrification processes (napA) were increased from 1.01-4.38-fold at 10°C, which might have contributed to the bacterium's highly efficient nitrogen removal performance at low temperatures. Overall, this study offers valuable insights into transcriptome, and enhances the comprehension of the low-temperature-tolerant mechanism of simultaneous nitrification and denitrification processes.

Double cross-linked chitosan sponge encapsulated with ZrO2/soy protein isolate amyloid fibrils nanoparticles for the fluoride ion removal from water

Fluoride ion pollution in water has become a serious threat to the water environment and human health. Adsorption is a promising means of fluoride removal, but it also faces challenges such as the difficult separation and recovery of powdered particles, the leaching of modified coatings from adsorbents, and the structural disintegration of macroscopic adsorbents. For addressing the above challenges, glutaraldehyde/polyvinyl alcohol co-crosslinked ZrSAF/chitosan spongy composites (ZrS/GPCS) were prepared by utilizing encapsulation strategies and cross-linking. ZrS/GPCS-1, ZrS/GPCS-3 and ZrS/GPCS-4 were prepared due to the different amounts of cross-linking agents. The results showed that their fluoride ion adsorption capacities were 42.02, 44.44 and 39.84 mg/g, respectively. The removal of fluoride ions by ZrS/GPCS was maintained at >80 % in the pH range of 4–10. The addition of glutaraldehyde and polyvinyl alcohol affected the contact efficiency of fluoride ions with chitosan and ZrSAF, influencing the adsorption rate and adsorption effect. Glutaraldehyde, polyvinyl alcohol and ZrSAF improved the thermal stability, mechanical properties and structural integrity of chitosan matrix. Both the chitosan matrix and the internal ZrSAF played an important role in fluoride removal, and the removal mechanisms included electrostatic interaction, hydrogen bonding, and complexation.

Eriophyid mites in fruit crops: Biology, ecology, molecular aspects, and innovative control strategies

Eriophyid mites, minute arachnids within the family Eriophyidae, pose significant threats to fruit crops globally, leading to substantial economic losses in agriculture. This comprehensive review aims to elucidate the intricate biology, ecology, molecular aspects, and innovative control strategies of these pervasive pests. Eriophyid mites exhibit a complex life cycle and reproductive strategy, with their habitat preferences and distribution heavily influenced by environmental factors and host-plant interactions. Advances in molecular biology have provided more profound insights into their genetics and interactions at the molecular level, revealing crucial information for developing targeted pest management strategies. Control strategies for eriophyid mites encompass chemical methods, such as applying acaricides and understanding resistance mechanisms, as well as biological control using natural predators and parasitoids. Cultural and physical control methods, including crop rotation and mechanical removal, play vital roles in integrated pest management (IPM). Emerging approaches like RNA interference (RNAi) and semiochemical-based controls offer promising alternatives for sustainable pest management. This review underscores the importance of a multifaceted approach to effectively manage eriophyid mite infestations, integrating traditional and novel strategies. Future research should focus on overcoming current challenges, enhancing the efficacy of control methods, and further exploring the molecular mechanisms underlying mite-plant interactions

Boron removal from wastewater via coordinative adsorption assisted by Fenton-Induced Oxoprecipitation/Flocculation

Chemical precipitation is widely used for boron removal from water in industrial-scale processes, though a following post treatment is generally required to meet the concentration set by current international standards.In this work, chemical precipitation of boron (B) in water by different precipitating agents was combined with Fenton treatment to enhance the boron removal effectiveness. This approach achieved residual boron concentration of less than 0.5 mg/L, hard to achieve through conventional precipitation methods.Batch tests were performed at different dosage of Fenton reagents, and selected Fe2+/H2O2 weight ratios were evaluated with or without adding precipitating agents. The effect of pH on the process was also investigated, to assess the optimal conditions to maximize boron removal. At the end of the process, barium hydroxide was used to remove effectively excess sulfate ions.The sludge produced was characterized by XRD, SEM and FTIR analysis, and the mechanism of boron removal was investigated.An oxoprecipitation mechanism was induced by the Fenton process: boron-based species were converted into borate ion, thus predisposing them to a coordination-type adsorption on the surface of iron and calcium hydroxide, assisted by aluminum sulfate at pH 12.5.The process was then successfully tested on real boron −contaminated wastewater, thus confirming the effectiveness of the process while simultaneously decreasing the organic content.

Mechanisms of mercury removal from water with highly efficient MXene and silver-modified polyethyleneimine cryogel composite filters

Safeguarding aquatic ecosystems and human health requires effective methods for removing pollutants. Mercury (Hg) is a very toxic pollutant with a global presence and is highly mobile and persistent. Here, innovative materials were prepared for separating Hg(II) from water, and the mechanisms underlying the efficient uptake of Hg species have been investigated. The sorbents include silver (Ag) nanoparticles and multilayered Ti3C2Tx MXene, both incorporated into the structure of a three-dimensional polyethyleneimine porous cryogel (PEI) that acts as a scaffold holding and exposing nano active sites involved in the removal of Hg. Specifically, Ag particles were deposited onto MXene phases, and the resulting composite was embedded in the macroporous PEI polymer (PEI/MXene@Ag cryogel). The composite has beneficial properties regarding Hg removal: 99% of Hg was separated from waste within 24 h in batch studies. The maximum removal capacity of Hg reached 875 mg/g from HgCl2, and 761 mg/g and 1280 mg/g from Hg(OAc)2 and Hg(NO3)2 salts by PEI/MXene@Ag. The Hg uptake stems from the composite’s relatively large specific surface area, layered porous channels, and highly dispersed Ag nanoparticles in the multilayered Ti3C2Tx MXene. The matrix in the water samples that were treated with the composite did not hinder the uptake of Hg by PEI/MXene@Ag. The high effectiveness achieved for the removal of Hg, combined with rapid adsorption kinetics, high efficiency, and selectivity, positions it as an efficient solution. Future work should address upscaling its preparation for increasing readiness towards mitigating Hg in surface water.

Resource recovery of water treatment plant sludge and river sediment as phosphorus removal material: feasibility and mechanisms

ABSTRACT Excessive phosphorus is a critical contributor to eutrophication, necessitating the use of substantial amounts of phosphorus removal materials. To address the challenge of managing water treatment plant sludge and river sediment while also supplying mass-produced phosphorus-removing materials for projects targeting phosphorus removal in water bodies, this paper attempted to study the feasibility of preparing phosphorus removal materials by mixing and calcining water treatment plant sludge and river sediment (C-WTPS/RS). The study examined the transformation of phosphorus forms in C-WTPS/RS before and after adsorption. Furthermore, X-ray fluorescence spectrometer, zeta potential, scanning electron microscope, Brunauer–Emmett–Teller equation, Barrett–Joyner–Halenda model, X-ray photoelectron spectroscopy, and Fourier transform infrared spectroscopy were employed to elucidate the phosphorus removal mechanisms. The results showed that C-WTPS/RS was effective in removing phosphorus from water and preventing the release of phosphorus from the sediment. Additionally, C-WTPS/RS had a low risk of releasing phosphorus and metals within the pH range of natural water bodies. These proved that it is feasible to remove phosphorus by C-WTPS/RS. After adsorption, the increased phosphorus in C-WTPS/RS was mainly dominated by the non-apatite inorganic phosphorus within inorganic phosphorus. The main phosphorus removal mechanisms of C-WTPS/RS were physical adsorption, electrostatic adsorption, chemical precipitation, and ligand exchange.