Removal Efficiency Research Articles

Efficient removal of COD, BOD, oil & grease, and turbidity from oil-field produced water via electrocoagulation treatment.

The simple design, compactness, simultaneous treatment of multiple contaminants, absence of chemical usage, minimal sludge formation (reducing secondary pollution), low maintenance cost, and versatility to operate in both batch and continuous modes make electrocoagulation (EC) a promising choice for treating various types of industrial wastewater. In this study, EC was employed in batch mode to treat produced water obtained from an oil drilling site, to reuse it for injection purposes in the reservoir. Produced water typically contains high levels of total dissolved solids (TDS), turbidity, chemical oxygen demand (COD), biological oxygen demand (BOD), and oil & grease (O&G) contaminants. High-performing aluminum (Al) electrodes were chosen due to their stability, conductivity, and, most significantly, their high capacity for generating aluminum hydroxide ([Al(OH)₃]ₙ) flocs, which serve as carriers for contaminant capture. This compound has demonstrated remarkable effectiveness in trapping the aforementioned contaminants from produced water under various operating conditions, including the number of electrodes, supplied current, and electrode configuration (bipolar and monopolar). The impact of several factors, including the number of electrodes (varying from 4 to 8), current density (varying as 16, 79, 158 A/m2), and electrode configuration (bipolar and monopolar), was studied at room temperature and 250rpm agitation speed. Initial turbidity, COD, BOD, and O&G concentrations were measured at 38 NTU, 700.7ppm, 120ppm, and 32.8ppm, respectively. The EC treatment exhibited removal efficiencies of 51% for TDS, 85% for turbidity, 78% for COD, 80% for BOD, and 85% for O&G using a monopolar configuration with 8 electrodes, and 59% for TDS, 90% for turbidity, 85% for COD, 84% for BOD, and 86% for O&G using a bipolar configuration with eight electrodes. Additionally, cost estimation, considering electrode dissolution rate and power requirements, was conducted for the operation of both configurations.

Kinetic Modelling of Aromaticity and Colour Changes during the Degradation of Sulfamethoxazole Using Photo-Fenton Technology

Sulfamethoxazole (SMX) is an antibiotic that is extensively used in veterinary medicine, and its occurrence in wastewater and surface water can reach up to 20 μg/L. SMX is categorized as a pollutant of emerging concern by the US EPA due to its persistence and effects on humans and the environment. In this study, photo-Fenton technology is proposed for the removal of SMX. Aqueous solutions of SMX (50.0 mg/L) are treated in a 150 W UV photoreactor, using [Fe2+]0 = 0.5 mg/L and varying [H2O2]0 = 0–3.0 mM. During the reaction, colour (AU) was assessed along with SMX (mg/L), turbidity (NTU), and TC (mg/L). SMX degrades to aromatic intermediates with chromophoric groups, exhibiting colour (yellow to brown) and turbidity. As these intermediates are mineralized into CO2 and H2O, the colour and turbidity of the water lose intensity. Using a molar ratio of 1 mol SMX:10 mol H2O2, the maximum degradation of aromatic species takes place (71% elimination), and colourless water with turbidity < 1 NTU is obtained. A kinetic modelling for aromaticity loss and colour formation as a function of the oxidant concentration has been proposed. The application of this model allows the estimation of oxidant amounts for an efficient removal of SMX under environmentally friendly conditions.

Efficient Removal of PFASs Using Photocatalysis, Membrane Separation and Photocatalytic Membrane Reactors.

Perfluoroalkyl and polyfluoroalkyl substances (PFASs) are persistent compounds characterized by stable C-F bonds giving them high thermal and chemical stability. Numerous studies have highlighted the presence of PFASs in the environment, surface waters and animals and humans. Exposure to these chemicals has been found to cause various health effects and has necessitated the need to develop methods to remove them from the environment. To date, the use of photocatalytic degradation and membrane separation to remove PFASs from water has been widely studied; however, these methods have drawbacks hindering them from being applied at full scale, including the recovery of the photocatalyst, uneven light distribution and membrane fouling. Therefore, to overcome some of these challenges, there has been research involving the coupling of photocatalysis and membrane separation to form photocatalytic membrane reactors which facilitate in the recovery of the photocatalyst, ensuring even light distribution and mitigating fouling. This review not only highlights recent advancements in the removal of PFASs using photocatalysis and membrane separation but also provides comprehensive information on the integration of photocatalysis and membrane separation to form photocatalytic membrane reactors. It emphasizes the performance of immobilized and slurry systems in PFAS removal while also addressing the associated challenges and offering recommendations for improvement. Factors influencing the performance of these methods will be comprehensively discussed, as well as the nanomaterials used for each technology. Additionally, knowledge gaps regarding the removal of PFASs using integrated photocatalytic membrane systems will be addressed, along with a comprehensive discussion on how these technologies can be applied in real-world applications.

Green synthesis of ZnO and Ni-doped ZnO from okra stalks for the photocatalytic degradation of Procion Red MX-5B

This study investigates the photocatalytic degradation of Procion Red MX-5B (PRM) using ZnO and Ni-doped ZnO catalysts derived from okra stalks through a green synthesis method. Various parameters, including hydrogen peroxide concentration (HPC), catalyst amount, nickel (Ni) doping amount, initial PRM concentration, and pH, are systematically studied to assess their impact on PRM degradation efficiency. The results reveal that both ZnO and Ni-doped ZnO catalysts exhibit promising photocatalytic activity, with the highest PRM degradation efficiency achieved at the following reaction conditions: 6 mM of HPC, 40 mg of Ni(7%):ZnO catalyst, 10 ppm initial PRM concentration, and pH = 6. Under these conditions, the Ni-doped ZnO catalyst demonstrated a degradation efficiency of 98.08% compared to 82.99% for the ZnO catalyst. The study highlights the potential of these catalysts for efficient organic pollutant removal and provides valuable insights into the factors influencing their photocatalytic performance.

A Sustainable Solution for the Adsorption of C.I. Direct Black 80, an Azoic Textile Dye with Plant Stems: Zygophyllum gaetulum in an Aqueous Solution.

The presence of pollutants in water sources, particularly dyes coming by way of the textile industry, represents a major challenge with far-reaching environmental consequences, including increased scarcity. This phenomenon endangers the health of living organisms and the natural system. Numerous biosorbents have been utilized for the removal of dyes from the textile industry. The aim of this study was to optimize discarded Zygophyllum gaetulum stems as constituting an untreated natural biosorbent for the efficient removal of C.I. Direct Black 80, an azo textile dye, from an aqueous solution, thus offering an ecological and low-cost alternative while recovering the waste for reuse. The biosorbent was subjected to a series of characterization analyses: scanning electron microscopy (SEM), thermogravimetric analysis (TGA), Brunauer-Emmett-Teller (BET) method, X-ray diffraction (XRD), and infrared spectroscopy (IR) were employed to characterize the biosorbent. Additionally, the moisture and ash content of the plant stem were also examined. The absorption phenomenon was studied for several different parameters including the effect of the absorption time (0 to 360 min), the sorbent mass (3 to 40 g/L), the pH of the solution (3 to 11), the dye concentration (5 to 300 mg/L), and the pH of the zero-charge point (2-12). Thermodynamic studies and desorption studies were also carried out. The results showed that an increase in plant mass from 3 to 40 g/L resulted in a notable enhancement in dye adsorption rates, with an observed rise from 63.96% to 97.08%. The pH at the zero-charge point (pHpzc) was determined to be 7.12. The percentage of dye removal was found to be highest for pH values ≤ 7, with a subsequent decline in removal efficiency as the pH increased. Following an initial increase in the amount of adsorbed dye, equilibrium was reached within 2 h of contact. The kinetic parameters of adsorption were investigated using the pseudo-first-order, pseudo-second-order and Elovich models. The results indicated that the pseudo-first-order kinetic model was the most appropriate for the plant adsorbent. The isotherm parameters were determined using the Langmuir, Frendlich, Temkin, and Dubinin-Radushkevich models. The experimental data were more satisfactory and better fitted using the Langmuir model for the adsorption of dye on the plant. This study demonstrated that Zygophyllum gaetulum stems could be employed as an effective adsorbent for the removal of our organic dye from an aqueous solution.

Continuous Fixed Bed Bioreactor for the Degradation of Textile Dyes: Phytotoxicity Assessment

This study explores a novel bioremediation approach using a continuous upflow fixed bed bioreactor with date pedicels as a biosupport material. Date pedicels offer a dual advantage: providing microbial support and potentially acting as a biostimulant due to their inherent nutrients. This research is divided into two phases: with and without microbial introduction. The bioreactor’s efficiency in removing two common textile dyes, RB19 and DR227, was evaluated under various conditions: fixed bed high, the effect of the initial concentration of the pollutant, and recycling the RB19 solution within the bioreactor. Optimization studies revealed an 83% removal yield of RB19 dye with an initial pollutant concentration of 100 mg·L−1 using activated sludge as inoculum. The bioreactor developed its own bacterial consortium without initial inoculation. Microscopic analysis confirmed the presence of a diverse microbial community, including protozoa (Aspidisca and Paramecium), nematodes, and diatoms. The bioreactor exhibited efficient removal of RB19 across a range of initial concentrations (20–100 mg/L) with similar removal efficiencies (around 65%). Interestingly, the removal efficiency for DR227 was concentration-dependent. The bioreactor demonstrated the ability to enhance the biodegradability of treated RB19 solutions. Phytotoxicity tests using watercress and lettuce seeds revealed no negative impacts on plant growth. SEM and FTIR analyses were conducted to examine the biosupport material before and after biotreatment.

Performance analysis of wire-electrochemical discharge cutting of glass material

The present study investigated the feasibility of micro-cutting in glass material by using Electrochemical Discharge Machining (ECDM) Process. Glass possesses outstanding properties that make it a versatile with widely used in a diverse range of applications. Because of its tendency to fracture brittle during machining, glass is typically processed in its liquid or viscous state to manufacture precise and high-quality parts. Machining glass with good dimensional accuracy is a challenging task due to its fragile nature. Therefore, researchers have recognized the very appropriate technique for machining glasses with precision. The Wire-Electrochemical Discharge Machining (WECDM) has been identified as the most economical and efficient technique for fabricating micro slits in thin glass samples. In the present work, an in-house setup for WECDM was developed and the feasibility of the developed configuration was examined. Two different thicknesses of glass specimen have been considered for experimentation for checking the quality of cut and it is found that thinner specimen possesses good quality cut. The regression model has been developed to find a relationship between input and response parameters. The developed regression model was reasonably well fitted with the observed values where applied voltage 55V, 15% by wt. electrolyte concentration and 70% duty cycle were the most influencing parametric combinations among others. Further mixed electrolytes have shown excellent performance up to a certain concentration in terms of Material Removal Rate (MRR). This study reveals that optimal capillary action, influenced by surface tension and electrolyte concentration, is crucial for consistent sparking and efficient material removal in WECDM.

Mangroves Invaded by Spartina alterniflora Loisel: A Remote Sensing-Based Comparison for Two Protected Areas in China

Mangroves are one of the world’s most productive and ecologically important ecosystems, and they are threatened by the widespread invasion of Spartina alterniflora Loisel in China. As few studies have examined the spatial pattern differences of S. alterniflora invasion and the nearby mangroves in different latitudes, we chose the Zhangjiang Estuary and the Dandou Sea, two representative mangrove–salt marsh ecotones in the north and south of the Tropic of Cancer, as the study areas for comparison. The object-based image analysis and visual interpretation methods were combined to construct fine-scale mangrove and S. alterniflora maps using high-resolution satellite imagery from 2005 to 2019. We applied spatial analysis, centroid migration, and landscape indexes to analyze the spatio–temporal distribution changes of mangroves and S. alterniflora in these two ecotones over time. We used the landscape expansion index to investigate the S. alterniflora invasion process and expansion patterns. The annual change rates of mangrove and S. alterniflora areas in the Zhangjiang Estuary showed a continuous growth trend. However, the mangrove areas in the Dandou Sea showed a fluctuating trend of increasing, decreasing, and then increasing again, while S. alterniflora areas kept rising from 2005 to 2019. Spartina alterniflora showed larger annual change rates compared with mangroves, indicating rapid S. alterniflora invasion in the intertidal zones. The opposite centroid migration directions of mangroves and S. alterniflora and the decreasing distances between the mangrove and S. alterniflora centroids indirectly revealed the fierce competition between mangroves and S. alterniflora for habitat resources. Both regions saw a decrease in mangrove patch integrality and connectivity. The integrality of mangrove patches in the Zhangjiang Estuary was always higher than those in the Dandou Sea. We observed the growth stage (2011–2014) and outbreak stage (2014–2019) of S. alterniflora expansion in the Zhangjiang Estuary and the outbreak stage (2005–2009) and plateau stage (2009–2019) of S. alterniflora expansion in the Dandou Sea. The expansion pattern of S. alterniflora varies in time and place. Since the expansion of S. alterniflora in the outbreak stage is rapid, with a large annual change rate, early warning of S. alterniflora invasion is quite important for the efficient and economical removal of the invasive plant. Continuous and accurate monitoring of S. alterniflora is highly necessary and beneficial for the scientific management and sustainable development of coastal wetlands.

Efficient Dye Removal by SA-g-P(AA-co-NIPAM/BENT) Composite Hydrogel

Efficient Dye Removal by SA-g-P(AA-co-NIPAM/BENT) Composite Hydrogel

Highly efficient removal of trace thallium from surface water by Co@Fe Prussian blue analogue coated membrane

Super trace thallium(I) (Tl+) is still highly toxic and its removal from surface water is challenging. Here, we developed a new adsorptive membrane by immobilizing bimetal (cobalt and iron) Prussian blue analogues (Co@Fe-PBAs) on a polytetrafluoroethylene microporous membrane (Co@Fe-PBAs-M). The prepared membrane displayed precise adsorption of trace Tl+ (50 μg/L) from complex water. A variety of interfering factors, such as water pH, competitive adsorption of positive ions (Na+ and K+) and negative ions (CO32– and PO43-), natural organic matters (e.g., fulvic acid and bovine serum albumin) were evaluated during Tl removal. The composite membrane showed high removal efficiency (over 80 %) during long-term dynamic membrane separation of surface water containing super trace Tl+ (<2.0 μg/L), breaking through the adsorption limitation in ultralow concentration of Tl+. The unique bimetal electron transfer of Co@Fe-PBAs-M reinforced the adsorptive performance to Tl+ through dual ion exchange and intercalation. In the treatment of real Pearl River water containing 0.5 μg/L of Tl+, our membrane effectively reduced the Tl+ concentration to 0.04 μg/L during 6-h continuous separation, which was far below the required level for drinking water (i.e., 0.1 μg/L). This work offers a promising solution for safe drinking water by remedying ultralow Tl+ contaminated surface water.

Effects and mechanisms of Fe/N co-doped magnetic biochar for efficient removal of single and multiple dye

Effects and mechanisms of Fe/N co-doped magnetic biochar for efficient removal of single and multiple dye

Periodic polarity reversal triggered sequential electrochemical redox of blue TiO2 nanotube arrays for efficient removal of antibiotics and inorganic nitrogen from actual mariculture wastewater

Using blue TiO2 nanotube arrays (Ti/BTNAs) as both anode and cathode, a novel bipolar system that is suitable for operating in periodic polarity reversal (PR) and flow-through mode was established, aiming to effectively remove antibiotics and inorganic nitrogen from actual mariculture wastewater. Under optimal conditions of 4.0 mA/cm2 current density, 3.0 mL/min water flow rate and 2.0 cycles/h polarity reversal frequency, the PR-induced synergistic effect endows Ti/BTNAs abundant oxygen vacancies (20.53 %), high activity and extended service lifetime (5.25 years), realizing continuous production of surface-adsorbed active hydrogen (Hads∗) at cathode and reactive chlorine species (Cl, ClO, Cl2−, ClO−) over anode through Cl− reacting with reactive oxygen species (HO, SO4−, O2−) and ∼0.7 kWh/gTOC energy consumption. Bipolar system can also flexibly regulate denitrification mechanism through the PR-triggered sequential electrochemical redox of Ti/BTNAs in water flow direction, achieving minimum energy consumption of ∼43.4 ± 3.2 kWh/kg(NH4+-N) and 33.7 ± 2.3 % current efficiency. Berberine antibiotic degradation pathway was suggested by DFT calculations and LC-MS/MS analyses. This study provides a long-acting and low-consuming strategy for comprehensive treating mariculture wastewater.

Palygorskite-mediated simultaneous nutrient removal and antibiotic degradation from aquaculture wastewater in lab-scale constructed wetlands

In this study, palygorskite was employed as a substrate in laboratory-scale constructed wetlands (CWs) over a period of 180 days to investigate the removal efficiency of pollutants from mariculture wastewater under high loads of enrofloxacin (ENR) stress. The results indicated that the incorporation of palygorskite into CWs resulted in average effluent concentrations of total phosphorus (TP), total nitrogen (TN), chemical oxygen demand (COD), and ENR reaching 0.07 ± 0.00 mg/L, 1.07 ± 0.06 mg/L, 11.57 ± 1.04 mg/L, and 0.047 ± 0.002 mg/L, respectively. The removal efficiencies reached 96.45 ± 0.04 %, 94.62 ± 0.27 %, 88.61 ± 1.22 %, and 91.14 ± 5.00 % respectively, with phosphorus removal significantly surpassing that reported for similar CWs. This superior performance was mainly attributed to the strong binding mechanisms between phosphorus and the metal oxides and hydroxides leached from the palygorskite. The palygorskite stimulated the secretion of extracellular polymeric substances (EPS), accelerated biofilm establishment, and enhanced the relative abundance of key functional bacteria associated with carbon, nitrogen, and antibiotic removal, thus achieving rapid denitrification and efficient organic matter removal. Monitoring of metals (Ca, Fe, Mn, and Cu) in the CWs effluent suggested that their presence was insufficient to affect cytoplasmic enzyme activity or cause oxidative stress damage to plants. In conclusion, palygorskite serves as an environmentally friendly, high-nutrient removal alternative, apt as a substrate for CWs.

Regeneration and Single Stage Batch Adsorber Design for Efficient Basic Blue-41 Dye Removal by Porous Clay Heterostructures Prepared from Al13 Montmorillonite and Pillared Derivatives.

Porous clay heterostructures are a hybrid precursor between the pillaring process and organoclays. In this study, the organoclay was substituted by an aluminium intercalated species clay or pillared alumina clays. A porous clay heterostructure was successfully achieved from an aluminium intercalated species clay, due to the easy exchange of the aluminium species by the cosurfactant and silica species. However, using alumina pillared clays, the porous clay heterostructures were not formed; the alumina species were strongly attached to clay sheets which made difficult their exchange with cosurfactant molecules. In this case, the silica species were polymerized and decorated the surface of the used materials as indicated by different characterization techniques. The specific surface area of the porous clay heterostructure material reached 880 m2/g, and total pore volume of 0.258 cc/g, while the decorated silica alumina pillared clays exhibited lower specific surface area values of 244-440 m2/g and total pore volume of 0.315 to 0.157 cc/g. The potential of the synthesized materials was evaluated as a basic blue-41 dye removal agent. Porous clay heterostructure material has a removal capacity of 279 mg/g; while the other materials exhibited lower removal capacities between 75 mg/g and 165 mg/g. The used regeneration method was related to the acidity of the studied materials. The acidity of the materials possessed an impact on the adopted regeneration procedure in this study, the removal efficiency was maintained at 80% of the original performance after three successive regeneration cycles for the porous clay heterostructure. The Langmuir isotherm characteristics were used to propose a single-stage batch design. Porous clay heterostructures with a higher removal capacity resulted in a decrease in the quantities needed to achieve the target removal percentage of the BB-41 dye from an aqueous solution.

Constructing Stable Nitrogen-Rich Core-Shell CdS@MC for Photocatalytic Reduction of U(VI) in Air without Sacrificial Agent.

Photocatalytic reduction of uranium from U(VI) to U(IV) has been recognized as an effective treatment method for uranium wastewater. However, most photocatalysts have to be reduced under inert gas and sacrificial agent. Here, a class of nitrogen-rich core-shell photocatalysts (CdS@MC) with high stability was successfully prepared by modifying CdS with melamine and cyanuric chloride condensation. When the initial concentration of U(VI) was 100 mg/L and the solid-liquid ratio was 0.2 g/L, the removal of U(VI) by CdS@MC without sacrificial agent under air could reached 95%. The removal rate was still above 80% after five cycles with good stability and good removal rate of U(VI) at high salt concentration. CdS@MC not only efficiently generates electrons for photocatalytic reduction of U(VI), but also generates H2O2 from O2, which then reacts with uranyl ions to produce metastudtite. This study provides a new direction for the study of efficient uranium removal photocatalysts without sacrificial agent in air environment.

Synthesis and application of Tb-MOF for efficient fluorescence detection and removal of tetracycline from aqueous environments

This study aimed to create and characterize a fluorescence-based Tb-MOF compound for the effective detection and removal of tetracycline (TC) from water-based environments. Tb-MOF was synthesized by a solvothermal method using 1,4-benzenedicarboxylic acid, 1,10-phenanthroline as organic ligands and Terbium (Tb) as the metal center. Tb-MOF exhibited very intense fluorescence emission at 545 nm when excited at 306 nm at room temperature. Tb-MOF exhibited high sensitivity and selectivity in detecting tetracycline, with a Ksv value of 8.56×108 M−1 in the concentration range of 0–60 µM and an impressive detection limit of 0.0245 µM. Additionally, the adsorption performance of Tb-MOF for tetracycline was evaluated by examining its basic parameters, such as reaction time, pH, temperature, and adsorbent dosage. The adsorption data obtained in this study were consistent with the Langmuir model, indicating a maximum adsorption capacity of 266.9 mg/g at 298 K. Moreover, the adsorption kinetics followed a pseudo-second-order kinetic model, with a rate constant of 0.00267 g/ (mg·min). Based on the real sample studies, it was concluded that Tb-MOF is a promising material for the detection and removal of tetracycline in complex systems.

Catalytic performance of FeCo2O4 spinel cobaltite for degradation of ethylparaben in a peroxymonosulfate activation process: Response surface optimization, reaction kinetics and cost estimation

The presence of cosmetics and personal care products in water resources has become an increasing concern for environment due to their toxicity and persistence in aquatic medium. Peroxymonosulfate mediated advanced oxidation methods have a great potential for the efficient removal of complex organic compounds due to the generation of highly reactive radicals with high oxidation ability. Iron cobaltite, FeCo2O4 catalyst was used as a peroxymonosulfate (PMS) activator for the degradation of ethylparaben which was selected as a model personal care product ingredient. Paraben degradation was modelled and the optimum operating parameters were determined by using Box-Behnken design. The ethylparaben degradation efficiency was calculated as 94.6 % under the optimized conditions which were determined as 0.9 g/L FeCo2O4 loading, pH 6.15, and 0.26 g/L PMS dosage. The ethylparaben degradation reaction followed second-order reaction kinetics. The activation energy was evaluated as 40.1 kJ/mol. Quenching radical tests showed that the dominant reactive species were hydroxyl radicals. Toxicity of the treated samples in terms of L. sativum growth inhibition was evaluated as 1.5 %. The total cost of the treatment including the operating and the amortization costs was calculated as 0.91 €/L.

Synthesis and characterization of Selenicereus undatus extract mediated nano-Bi2O3 and its application in the adsorption of Rhodamine B dye

Betacyanins (BC) are reddish-purple pigments widely found in the peels of white-fleshed dragon fruit (Selenicereus undatus) and peels and pulps of red-fleshed dragon fruit (Selenicereus costaricensis). BC pigments are good anti-oxidants that inhibit the formation of reactive oxygen species (ROS) in plants and thereby promote the reduction of metal ions to zero-valent metals. It also acts as a good stabilizing and capping agent in the synthesis of nanoparticles. Hence, this research aims to extract, and quantize the content of BC from the peels of Selenicereus undatus, to fabricate betacyanin-rich- Selenicereus undatus (SU) modified bismuth oxide nanoparticles (Bi2O3 NPs) and characterize using UV-Vis, FTIR, XRD, SEM, EDAX, and BET. The quantity and stability of the betacyanin are optimized using various parameters like time, temperature, solvent ratio, pH, etc., through a UV-Vis spectrophotometer at 538 nm. Synthesized SU-Bi2O3 NPs aim to alleviate synthetic dye contaminants through adsorption- an efficient route for water remediation. The nano-adsorbent Bi2O3 NPs showed an increase in dye adsorption with an increase in reaction time, temperature, and Bi2O3 NPs dosage, enabling efficient removal of dyes such as Rhodamine B (RhB) dyes.

Highly selective guanidine-linked covalent organic framework for efficient removal of perfluoroalkyl carboxylic acids from water samples

In this study, guanidine-linked covalent organic framework (TPDGCl) was synthesized via a solvothermal method. The presence of guanidine groups in its structure facilitates electrostatic interactions and provides hydrogen bonding sites, enabling the selective enrichment of perfluoroalkyl carboxylic acids (PFCAs) from environmental water samples. The material exhibits rapid kinetic mass transfer, which facilitates the efficient removal of samples containing PFCAs from aqueous solutions within 5 min. Furthermore, TPDGCl exhibits several advantageous properties, including high selectivity for PFCAs, a high adsorption capacity (2005 mg/g), excellent chemical stability, and remarkable recyclability (five cycles). Additionally, density functional theory (DFT) studies have demonstrated that the adsorption of PFCAs on TPDGCl is enhanced by ion exchange, hydrophobic interactions, hydrogen bonding interactions and ordered channel structures. Finally, TPDGCl was used as an adsorbent for dispersive solid-phase extraction (d-SPE), in combination with ultra-high performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS), to develop an analytical method for the efficient extraction and sensitive detection of PFCAs. The developed method exhibits highly sensitivity, with detection and quantification limits of 0.64–0.85 ng/L and 2.6–3.4 ng/L, respectively. The recoveries of actual water samples ranged from 75.4% to 113.7%. Moreover, TPDGCl effectively reduces the levels of PFCAs in real water samples to less than 70 ng/L within only 1 h. These results indicate that TPDGCl is an effective adsorbent for removing PFCAs from environmental water samples.

Fabrication of ultrafiltration membrane with antibacterial properties by blending Ag/UiO-66-NH2 and bamboo cellulose

Cellulose is a widely available organic substance that forms membranes with excellent hydrophilicity and biocompatibility. However, it is prone to biological contamination because its surface is conducive towards the accumulation of biologically active substances, which has hindered its application potential. In this work, an antimicrobial cellulose-based membrane (Ag/UiO-66-NH2@BCM) with high water flux, high retention rate, and good hydrophilicity was prepared. At an optimal blend ratio of 1 wt% Ag/UiO-66-NH2, the membrane exhibited significant improvements, including a 31% increase in pure water flux, a Bovine Serum Albumin retention rate of 99.6%, and a water flux recovery of 97.4%. Crucially, the membrane demonstrated potent antibacterial, showcasing its broad-spectrum antimicrobial properties. Investigations into the ability of Ag/UiO-66-NH2@BCM to remove Pb2+, Cd2+, and Cr6+ ions from a water column revealed that the maximum adsorption capacity of the monolayer was 405, 390, and 328 mg/g, respectively. The composite membrane demonstrated broad-spectrum and highly effective antimicrobial properties, along with efficient removal of heavy metal ions. The proposed method can be utilized to prepare other composite membranes for water treatment and other fields of membrane separation technology.