High Distribution Coefficient Research Articles

High Performance and Selective Sequestration of Cd(II) from Water by Layered Thiophosphate.

The extensive use of toxic cadmium (Cd) in energy conversion and industrial applications ranging from solar cells and battery appliances to paints and pigments contaminates water bodies. However, the upper limit of Cd contamination in drinking water is to be only 3 ppb by the WHO and 5 ppb by the USA-EPA, which underscores the need for cost-effective, efficient, and ppb level capture of Cd from contaminated water. Leveraging the selectivity due to Lewis's hard-soft acid-base (HSAB) theory, we have achieved swift and highly selective capture of Cd(II) ions from aqueous mediums using layered potassium manganese thiophosphate (K-MnPS3). K-MnPS3 effectively removes Cd(II) ions from extremely dilute aqueous solutions (ppb levels), achieving a maximum sorption capacity of 405.43 mg/g and a removal rate exceeding 97% within 20 min. Even in the presence of competing ions such as Na+, Mg2+, Ca2+, and Pb2+, K-MnPS3 remains selective. Additionally, it operates efficiently across a wide pH range (1.78-11.19) with a high distribution coefficient (∼104 mL/g). Breakthrough experiments using a 1 wt % K-MnPS3 and 99 wt % sand column showed complete breakthrough of Cd(II) after 62 h, leading K-MnPS3 as a promising candidate for Cd(II) removal from industrial effluents.

STUDY OF NON-FUEL APPLICATION OF BROWN COAL DERIVATIVES IN THE PRODUCTION OF MEMBRANES BASED ON HYBRID BIODEGRADABLE MATERIALS

The article shows research into the non-fuel use of brown coal derivatives in the production of membranes based on hybrid biodegradable materials. The work used polylactide brand Terramac TP-4000, humic substances obtained from brown coals. Membranes for water purification from heavy metals were obtained from hybrid biopolymer materials based on pol- ylactide and humic substances in the form of polymer porous films with a pore size of 20 microns and a working surface area of the membrane of 28.26∙10-4 m2 with a circle diameter of 6 cm. Used in our The work of humic substances belonged to the group of well-hummified, more aromatic with a high content of acidic functional groups, which leads to their high com- plexing ability to form stable metal-humic complexes. The developed hybrid biodegradable materials based on polylactide and humic substances were used as highly effective sorption membrane materials to reduce the content of heavy metals in aqueous solutions. Obtaining membranes of hybrid biodegradable materials based on polylactide and humic substances have maximum selectivity for the extraction of metal ions in relation to Cu2+ – 95 % and Pb2+ – 94 %; and for metals such as Cd2+, Hg2+, Zn2+ and Co2+, it ranges from 82 to 89 %. Comparing the percentage of metal ions adsorbed, it can be seen that the easiest adsorbed metal was lead, copper and zinc adsorbed similarly, with cadmium showing the lowest percentage, but its adsorption was slightly worse than in the case of copper and zinc. The highest value was obtained for single adsorption of Cu2+ ions; in the case of adsorption from a mixture, this metal also had the highest distribution coefficient, and strong adsorption was also found for Pb2+. On the other hand, the adsorption of Zn2+ was, according to the “partition coefficient,” relatively weak. Strong and residual phases were highest for copper and lead, these two metals were largely bound into strong complexes by humic substances and only a very small amount could be washed out under normal conditions. It was found that the leaching of metal ions from mem- brane hybrid biodegradable materials based on polylactide and humic substances into water was very low, in most cases it was about 10 % and did not exceed 20 %. Most of the metal ions (≥60 %) were very tightly bound and were partially leached out under strongly acidic conditions. The obtained results of adsorption resistance vary significantly and correlate well with the age and degree of humification of humic substances.

Selective and antibacterial zinc phosphonate framework system for superior marine uranium harvesting

Efficient utilization of uranium in seawater provides a viable and sustainable solution to supply the growing demand for nuclear energy. Adsorbents used for uranium extraction from seawater are usually disturbed by co-existing ions and contaminated by organisms. In this study, a zinc phosphonate framework system (ZMP2-6) with zoledronic acid as a ligand was fabricated via a facile one-step mixing method at room temperature, which possesses great adsorption performance, high selectivity and outstanding antibacterial ability. The high porosity and rich binding sites endowed ZMP2-6 with an extremely high adsorption capacity of 1695.5 mg/g at 25°C. Remarkably, ZMP2-6 selectively extracted 18.0 mg/g uranium from natural seawater in only 1 month with a higher distribution coefficient against other coexisting metal ions. In addition, ZMP2-6 exhibited excellent bacteriostatic ability against Staphylococcus aureus (S. aureus) and Escherichia coli (E. coli), which was greatly desired in real uranium extraction from seawater. Noteworthily, ZMP2-6 can be easily assembled into adsorption modules and grow on different carriers, which significantly improves uranium separation efficiency and practical applicability. This work rationally engineered a zinc phosphonate framework system and provided a strategy for highly efficient uranium capture from the ocean.

Record High Iodate Anion Capture by a Redox-Active Cationic Polymer Network.

As a critical radioactive anionic contaminant, traditional adsorbents primarily remove iodate (IO3 -) through ion exchange or hard acid-hard base interactions, but suffer from limited affinity and capacity. Herein, employing the synergistic effect of ion exchange and redox, we successfully synthesized a redox-active cationic polymer network (SCU-CPN-6, [C9H10O2N5 ⋅ Cl]n) by merging guanidino groups with ion-exchange capability and phenolic groups with redox ability via a Schiff base reaction. SCU-CPN-6 exhibits a groundbreaking adsorption capacity of 896 mg/g for IO3 -. The inferior adsorption capacities of polymeric networks containing only redox (~0 mg/g) or ion exchange (232 mg/g) fragments underscore the synergistic "1+1>2" effect of the two mechanisms. Besides, SCU-CPN-6 shows excellent uptake selectivity for IO3 - in the presence of high concentrations of SO4 2-, Cl-, and NO3 -. Meanwhile, a high distribution coefficient indicates its exemplary deep-removal performance for low IO3 - concentration. The synergic strategy not only presents a breakthrough solution for the efficient removal of IO3 - but also establishes a promising avenue for the design of advanced adsorbents for diverse applications.

Record High Iodate Anion Capture by a Redox‐Active Cationic Polymer Network

AbstractAs a critical radioactive anionic contaminant, traditional adsorbents primarily remove iodate (IO3−) through ion exchange or hard acid‐hard base interactions, but suffer from limited affinity and capacity. Herein, employing the synergistic effect of ion exchange and redox, we successfully synthesized a redox‐active cationic polymer network (SCU‐CPN‐6, [C9H10O2N5 ⋅ Cl]n) by merging guanidino groups with ion‐exchange capability and phenolic groups with redox ability via a Schiff base reaction. SCU‐CPN‐6 exhibits a groundbreaking adsorption capacity of 896 mg/g for IO3−. The inferior adsorption capacities of polymeric networks containing only redox (~0 mg/g) or ion exchange (232 mg/g) fragments underscore the synergistic “1+1>2” effect of the two mechanisms. Besides, SCU‐CPN‐6 shows excellent uptake selectivity for IO3− in the presence of high concentrations of SO42−, Cl−, and NO3−. Meanwhile, a high distribution coefficient indicates its exemplary deep‐removal performance for low IO3− concentration. The synergic strategy not only presents a breakthrough solution for the efficient removal of IO3− but also establishes a promising avenue for the design of advanced adsorbents for diverse applications.

A 2D Acridine‐Based Covalent Organic Framework for Selective Detection and Efficient Extraction of Gold from Complex Aqueous‐Based Matrices

AbstractDeveloping candidate materials which possess the ability of both selective detection and efficient capture of precious metal gold is highly desirable for environment and economy. However, most of reported materials only focus on single function, which seriously restricts their practical application as probes or adsorbents. Herein, a two dimensional (2D) acridine‐based covalent organic framework (TpDa‐COF) is prepared via the linkage of imine bonds for gold detection and adsorption. The synthesized COF can achieve both fluorescence and colorimetric dual sensing for Au3+ in a low concentration range (0.1–1.5 ppm) with the limit of detection (LOD) of 0.036 ppm. Impressively, the selectivity of TpDa‐COF for the detection of Au3+ is admirable (Fe3+, Fe2+ and Cu2+ for negligible influence on its fluorescence). In addition, TpDa‐COF exhibits ultrahigh adsorption capacity of 982.5 mg ⋅ g−1 for gold at pH=4, which is attributed the synergistic effect of both selective coordination and reductive process of Au(III) to Au(0). Meanwhile, both positive entropy change (ΔS=76.07 J ⋅ mol−1 ⋅ K−1) and high distribution coefficient (Kd=12484.8 mL ⋅ g−1) confirm the good affinity between TpDa‐COF framework and gold. This work gives us a new insight to prepare COF with pyridine nitrogen sites for gold detection and adsorption.

A 2D Acridine-Based Covalent Organic Framework for Selective Detection and Efficient Extraction of Gold from Complex Aqueous-Based Matrices.

Developing candidate materials which possess the ability of both selective detection and efficient capture of precious metal gold is highly desirable for environment and economy. However, most of reported materials only focus on single function, which seriously restricts their practical application as probes or adsorbents. Herein, a two dimensional (2D) acridine-based covalent organic framework (TpDa-COF) is prepared via the linkage of imine bonds for gold detection and adsorption. The synthesized COF can achieve both fluorescence and colorimetric dual sensing for Au3+ in a low concentration range (0.1-1.5 ppm) with the limit of detection (LOD) of 0.036 ppm. Impressively, the selectivity of TpDa-COF for the detection of Au3+ is admirable (Fe3+, Fe2+ and Cu2+ for negligible influence on its fluorescence). In addition, TpDa-COF exhibits ultrahigh adsorption capacity of 982.5 mg ⋅ g-1 for gold at pH=4, which is attributed the synergistic effect of both selective coordination and reductive process of Au(III) to Au(0). Meanwhile, both positive entropy change (ΔS=76.07 J ⋅ mol-1 ⋅ K-1) and high distribution coefficient (Kd=12484.8 mL ⋅ g-1) confirm the good affinity between TpDa-COF framework and gold. This work gives us a new insight to prepare COF with pyridine nitrogen sites for gold detection and adsorption.

Ultrafast Removal of Thorium and Uranium from Radioactive Waste and Groundwater Using Highly Efficient and Radiation-Resistant Functionalized Triptycene-Based Porous Organic Polymers.

Thorium (Th) and uranium (U) are important strategic resources in nuclear energy-based heavy industries such as energy and defense sectors that also generate significant radioactive waste in the process. The management of nuclear waste is therefore of paramount importance. Contamination of groundwater/surface water by Th/U is increasing at an alarming rate in certain geographical locations. This necessitates the development of strategic adsorbent materials with improved performance for capturing Th/U species from radioactive waste and groundwater. This report describes the design of a unique, robust, and radiation-resistant porous organic polymer (POP: TP-POP-SO3NH4), which demonstrates ultrafast removal of Th(IV) (<30 s)/U(VI) (<60 s) species present in simulated radioactive wastewater/groundwater samples. Thermal, chemical, and radiation stabilities of these POPs were studied in detail. The synthesized ammoniated POP revealed exceptional capture efficiency for trace-level Th (<4 ppb) and U (<3 ppb) metal ions through the cation-exchange mechanism. TP-POP-SO3NH4 shows a significant sorption capacity [Th (787 mg/g) and U (854 mg/g)] with an exceptionally high distribution coefficient (Kd) of 107 mL/g for Th. This work also demonstrates a facile protocol to convert a nonperforming POP, by simple chemical modifications, into a superfast adsorbent for efficient uptake/removal of U/Th.

Recovery of rare earth elements from mine wastewater using alginate microspheres encapsulated with zeolitic imidazolate framework-8

There is increasing demand and interest in efficient methods for the recovery of rare earth elements (REEs) from wastewater because of the growing concerns associated with the negative impacts of REEs-rich waste discharged on pristine ecosystems. Here, we designed a ZIF-8@ALG composite hydrogel by encapsulating zeolitic imidazolate frameworks-8 (ZIF-8) into sodium alginate and poly (vinyl alcohol) double cross-linked networks (ALG) for the recovery of REEs from mine wastewater. ZIF-8@ALG showed exceptional REEs adsorption performance with the most superior separation factor (Ho/Mn) of 597.5. For the REEs considered, the ZIF-8@ALG composite exhibited a preference for heavy REEs with high adsorption efficiencies (65.3 ∼ 97.2%) and distribution coefficients (2045.5 ∼ 28500.0 mL·g−1). Adsorption involved a combination of electrostatic attraction, complexation and ion exchange mechanisms. REEs adsorbed on ZIF-8@ALG could also be desorbed using sodium citrate via ion-exchange and complexation, thus achieving efficient REEs recovery. In addition, ZIF-8@ALG was stable and reusable, maintaining effective adsorption in wastewater over four consecutive cycles, where the optimal adsorption efficiency reached 80.0%. Overall, this study provided an effective and feasible method for the recovery of REEs in mine wastewater, and confirmed that ZIF-8-based materials have significant potential for REEs recovery applications in wastewater engineering treatment.

Microbially formed Mn(IV) oxide as a novel adsorbent for removal of Radium

Radioactivity of Ra isotopes in natural waters is of serious concern. Control of 226Ra concentrations in tailings ponds, which store waste from U ore extraction processes, is an important issue in mill tailings management. In this study, we tested microbially formed Mn(IV) oxide as an adsorbent for removal of Ra in water treatment. Biogenic Mn(IV) oxide (BMO) was prepared using a Mn(II)-oxidizing fungus, Coprinopsis urticicola strain Mn-2. First, adsorption experiments of Sr and Ba, as surrogates for Ra, onto BMO were conducted in aqueous NaCl solution at pH 7. Distribution coefficients for Ba and Sr were estimated to be ∼106.5 and ∼104.3 mL/g, respectively. EXAFS analysis indicated that both Sr and Ba adsorbed in inner-sphere complexes on BMO, suggesting that Ra would adsorb in a similar way. From these findings, we expected that BMO would work effectively in removal of Ra from water. Then, BMO was applied to remove Ra from mine water collected from a U mill tailings pond. Just 7.6 mg of BMO removed >98% of the 226Ra from 3 L of mine water, corresponding to a distribution coefficient of 107.4 mL/g for Ra at pH ∼7. The obtained value was convincingly high for practical application of BMO in water treatment. At the same time, the high distribution coefficient indicates that Mn(IV) oxide can be an important carrier and host phase of Ra in the environment.

ВЫДЕЛЕНИЕ ГИДРОПЕРОКСИДА ВТОР-БУТИЛБЕНЗОЛА ИЗ ПРОДУКТОВ ЖИДКОФАЗНОГО ОКИСЛЕНИЯ ВТОР-БУТИЛБЕНЗОЛА МЕТОДОМ ЭКСТРАКЦИИ

Hydroperoxides of alkylaromatic hydrocarbons are valuable products of organic synthesis, which are widely used as initiators of polymerization and liquid-phase oxidation of hydrocarbons, as well as an epoxidizing agent. In addition, hydroperoxides are intermediates in the production of phenol and its alkyl derivatives. In this paper, a method is proposed for the isolation of tertiary hydroperoxide of sec-butylbenzene from the products of its liquid-phase aerobic oxidation by extraction with aqueous solutions of various solvents (methanol, ethanol, isopropanol, dimethylformamide, acetone and acetonitrile). The influence of the nature of the solvent, its concentration and the initial concentration of hydroperoxide on this process has been studied. Based on the experimental data obtained, it was found that 75-80% solutions of methanol and ethanol were the most effective in the extraction process. A high distribution coefficient is observed for a 75% methanol solution and is 1.24. It has been shown that up to 60% of the hydroperoxide can be extracted by single extraction. Carrying out a five-stage extraction of products of liquid-phase oxidation of second-butylbenzene with a 75% ethanol solution makes it possible to obtain concentrated up to 95% sec-butylbenzene hydroperoxide. Its structure was confirmed by IR spectroscopy. In this case, the isolated unreacted hydrocarbon can be directed to re-oxidation while maintaining a high rate, conversion and selectivity of hydroperoxide formation. The resulting concentrated tertiary hydroperoxide of sec-butylbenzene was subjected to sulfuric acid decomposition in a methyl ethyl ketone medium. It has been established that the products of this reaction are phenol and methyl ethyl ketone. At room temperature and a catalyst content of 0.8% by weight phenol and methyl ethyl ketone with yields of 88 and 71%, respectively, were obtained from hydroperoxide loading.

A nanotrap infused ultrathin hybrid composite material for rapid and highly selective entrapment of 99TcO4.

99Tc is one of the potentially toxic radioactive substances owing to its long half-life and a high degree of environmental mobility. Hence, the sequestration of 99Tc from radioactive waste has become enormously important and a contemporary research priority. However, selective extraction of this species in its stable oxoanionic form (99TcO4 -) is very challenging on account of bottlenecks such as low charge density, less hydrophilic nature, etc. Herein, an ultrathin hybrid composite material has been strategically designed and fabricated by covalent anchoring of a chemically stable amino functionalized nanosized cationic metal-organic polyhedron with a positively charged robust ionic covalent organic framework. The resulting thin-layer-based hybrid composite presented multiple exfoliated exposed interactive sites, including a Zr(iv)-secondary building unit, amine and triaminoguanidine functional groups, which can selectively interact with TcO4 - oxoanions through a synergistic combination of electrostatic, H-bonding and various other supramolecular interactions. Thus synthesized function-tailored composite, by virtue of its multiple unique characteristics, manifested an ultrafast and very selective, high distribution coefficient (∼106 mL g-1), as well as recyclable entrapment of TcO4 - oxoanions from the complex mixture of superfluous (∼5000-fold) other interfering anions in both high and ultra-trace concentrations along with simulated nuclear waste and from different water systems. Dynamic flow-through experiments were conducted with the membrane of the hybrid material in simulated wastewater, which reduced the concentration of ReO4 - (surrogate of radioactive TcO4 -) to below the WHO permissible level with rapid sequestration kinetics and excellent selectivity over excessive competing anions.

ЭКСТРАКЦИЯ ЦЕЗИЯ И СТРОНЦИЯ ИЗ АЗОТНОКИСЛЫХ РАСТВОРОВ КРАУН-ЭФИРАМИ В ТЯЖЕЛЫХ РАЗБАВИТЕЛЯХ

The extraction ability of crown-ethers has been studied with respect to cesium and strontium from nitric acid solutions in heavyweight polar organic solvents: chloroform; 1,2-dichloroethane; bis(2-chloroethyl)ether; nitrobenzene; 1,1,7-trihydrododecafluoroheptyl alcohol. Using bis(2-chloroethyl)ether as a new polar solvent in the extraction processes of dibenzo21-crown-7 and 4,4' (5')-ditretbutyldibenzo-18-crown-6, rather high distribution coefficients of cesium are achieved (DCs) from solutions with a nitric acid concentration of 1-5 mol / dm3. In the extraction of dicyclohexyl-18-crown-6 strontium, the highest DSr values were obtained, using chlorine-substituted hydrocarbons and bis(2-chloroethyl)ether with an extraction maximum of 1-3 mol / dm3 HNO3, depending on the diluent used. Extraction systems based on selective crown-ethers in a solvent mixture for the joint extraction of cesium and strontium from chemically complex nitric acid solutions are proposed.

Surface structure regulating of silica adsorbent for the selective adsorption of heavy rare earth

Rare earth element (REE) is a strategic metal resource, heavy REE owns higher economic and strategic value compared with light rare earth elements. However, it is a great challenge for the separation of heavy rare earth ion efficiently in the solution with mixed rare earth ions due to the similar physicochemical properties of heavy and light REE. In this paper, the diglycolamide (DGA) modified silica adsorbents were prepared and applied to the selective adsorption of heavy earth ion Dy3+. The structure of DGA on the silica surface was regulated during the modifying processes to obtain DGAb-SiO2 and DGAs-SiO2 adsorbent, which was verified by FTIR and NMR characterization results. The adsorption results showed that the DGAb-SiO2 adsorbent owned a much higher distribution coefficient (Kd) value for the selective adsorption of Dy3+ than the DGAs-SiO2 adsorbent. The higher adsorption selectivity is likely due to the fixed carbon chain of the DGA group on the surface of DGAb-SiO2 adsorbent formed rigid spatial structures of the oxygen atoms, which will be favorable for the selective coordination of Dy3+. Besides its effectiveness in adsorption behavior, the DGAb-SiO2 adsorbent displayed excellent stability. The Kd value of DGAb-SiO2 for Dy3+ selective adsorption maintained a high level after four successive recycling runs. The adsorption kinetics results displayed that the adsorption of Dy3+ followed pseudo-second-order kinetic, and the adsorption process fitted the Langmuir isotherm model. Additionally, the same adsorption rules for the rare earth ions were observed over DGA-KIT-6 adsorbent, indicating the high universality of the surface modification to the adsorbent support, which will provide an intentional reference for the surface modification to other adsorbent support.

Nanotrap Grafted Anionic MOF for Superior Uranium Extraction from Seawater.

On-demand uranium extraction from seawater (UES) can mitigate growing sustainable energy needs, while high salinity and low concentration hinder its recovery. A novel anionic metal-organic framework (iMOF-1A) is demonstrated adorned with rare Lewis basic pyrazinic sites as uranyl-specific nanotrap serving as robust ion exchange material for selective uranium extraction, rendering its intrinsic ionic characteristics to minimize leaching. Ionic adsorbents sequestrate 99.8% of the uranium in 120 mins (from 20,000 ppb to 24 ppb) and adsorb large amounts of 1336.8mg g-1 and 625.6mg g-1 from uranium-spiked deionized water and artificial seawater, respectively, with high distribution coefficient, Kd U ≥ 0.97 × 106 mL g-1 . The material offers a very high enrichment index of ≈5754 and it achieves the UES standard of 6.0mg g-1 in 16 days, and harvests 9.42mg g-1 in 30 days from natural seawater. Isothermal titration calorimetry (ITC) studies quantify thermodynamic parameters, previously uncharted in uranium sorption experiments. Infrared nearfield nanospectroscopy (nano-FTIR) and tip-force microscopy (TFM) enable chemical and mechanical elucidation of host-guest interaction at atomic level in sub-micron crystals revealing extant capture events throughout the crystal rather than surface solely. Comprehensive experimentally guided computational studies reveal ultrahigh-selectivity for uranium from seawater, marking mechanistic insight.

Fiber-supported layered magnesium phosphate exhibits high caesium(I) capture capacity in water

Solid-supported adsorbents used for the sequestration of radiocaesium, a major hazardous nuclear fission byproduct, from water are limited by low uptake capacities, increasing the difficulty of radioactive solid waste reduction. This study dispersed potassium magnesium phosphate monohydrate (KMP), a promising Cs+ adsorbent, in polyacrylonitrile fibers (PANFs) to efficiently adsorb Cs+. The larger size of KMP compared to PANFs is conjectured to result in the exposure of some KMP particles, thereby minimizing any decline in their adsorption capacity. The KMP/PANF composite exhibited an adsorption capacity per unit mass of KMP that was nearly equal to that of the bare KMP powder, which was less than 3.52% on average. The composite adsorbent with 100 wt% KMP loading demonstrated the highest experimental capacity of 299 mg g–1 among all solid-supported adsorbents reported to date. It also exhibited relatively fast uptake kinetics (equilibration time = 1.0–4.0 h) and a high distribution coefficient (average value of 1.22 × 104 mL g–1 over pH 5.0–11). Overall, the newly developed KMP/PANF adsorbent exhibits great potential for the practical decontamination of radiocaesium-contaminated waters.

Cross-linked HMO/PVA nanofiber mats for efficient lithium extraction from Salt-lake

With the rapid expansion of the new energy industry and electronics market, the demand for lithium is growing rapidly, leading to a significant increase in the price of the metal. There has been great interest in lithium extraction from salt lakes. The powdered lithium ion-sieve (LIS) suffers from poor dispersion and difficult recovery. Composite polyvinyl alcohol (PVA) nanofiber mats with H1.6Mn1.6O4 (HMO) were prepared by electrostatic spinning and radiation induced cross-linking. HMO was immobilized in the nanofiber mats by covalent attachment, cross-linking and entrapment. Hydrophilicity of PVA, high porosity of nanofiber and cross-linked 3D network endow the HMO/PVA nanofiber mats good mechanical strength, excellent Li+ adsorption performance and long service life. 1/1-HMO/PVA nanofiber mats exhibit Li+ adsorption capacity of 30.1 mg/g in salt-lake brine, which was superior to most LIS-containing adsorbents. Even in real salt-lake water with very low Li concentration of 15.45 mg/L and high Mg/Li ratio of 1260/1, the nanofiber mats have an excellent adsorption capacity of 24.2 mg/g and high distribution coefficient of 9713.34 mL/g, which was close to that of HMO powder. After ten adsorption and elution repetitions Li+ adsorption capacity decreased less than 10%, which indicates the long-term stability of the HMO/PVA nanofiber mats. The loss rate of Mn is less than 5% and gradually decreases with the increase of the number of cycles. The present study demonstrates the potential application of HMO/PVA nanofiber mats for direct recovery of Li+ from salt-lake especially in low-grade high Mg/Li ratio liquid lithium ore where holds a large proportion of the typical salt-lakes in China.

Copper removal and recovery from electroplating effluent with wide pH ranges through hybrid capacitive deionization using CuSe electrode

In modern industry, selective extraction and recovery of Cu from strongly acidic electroplating effluent are crucial to reduce carbon emissions, alleviate resource scarcity, and mitigate water pollution, yielding considerable economic and environmental benefits. This study proposed a high-efficiency CuSe electrode to selectively remove Cu from electroplating effluent via hybrid capacitive deionization (HCDI). The potential of this electrode was thoroughly evaluated to assess its effectiveness. The CuSe electrode exhibited superior deionization performance in terms of Cu adsorption capacity, selectivity, and applicability in various water matrices. Specifically, under strong acid conditions (1 M H+), the CuSe electrode maintained an optimal adsorption capacity of 357.36 mg g−1 toward Cu2+. In systems containing salt ions, heavy metals, and actual electroplating wastewater, the CuSe electrode achieved a remarkable removal efficiency of up to 90% for Cu2+ with a high distribution coefficient Kd. Notably, the capacitive deionization (CDI) system demonstrated the simultaneous removal of Cu-EDTA. The removal mechanism was further revealed using ex-situ X-ray diffraction and X-ray photoelectron spectroscopy analyses. Overall, this study presents a practical approach that extends the capabilities of CDI platforms for effectively removing and recovering Cu from acidic electroplating effluent.

Extraction of C6 α-olefin against n-paraffin in coker naphtha with deep eutectic solvents: Quantum chemical calculations and experimental investigation

Extraction technology is often employed to separate olefin/paraffin mixtures due to the advantages of mature process, flexible operation, and large processing capacity. This work aims to investigate the effectiveness of novel deep eutectic solvents (DESs) for the extraction of 1-hexene/n-hexane model coker naphtha using a combination of simulations and experiments. The results showed that the aliphatic or aromatic groups in the hydrogen bond acceptors or hydrogen bond donors have a strong affinity for 1-hexene, and the components containing hydroxyl or aromatic groups possess the ability to provide protons, which is beneficial to dissolve 1-hexene. Combining the results of the melting point predicted by the group and group-interaction contribution model, three DESs, namely ethanolamine-sulfolane 1:5 (DES1), tetrabutylammonium bromide-bis[2-(2-hydroxyethoxy)ethyl] ether 1:4 (DES2), and methyltriphenylphosphonium bromide-Triethylene glycol 1:4 (DES3), were finally prepared. Then, quantum chemical calculations were used to investigate the separation mechanism between the DESs and 1-hexene/n-hexane, demonstrating single-center and multi-center hybrid weak hydrogen bonds dominated by the dispersion attraction between DESs and 1-hexene. Finally, liquid–liquid equilibrium experiments were used to examine the effects of DESs type, composition, and temperature on the separation performance, and the results showed that the DES1 has both high distribution coefficient of 1-hexene and selectivity of 1-hexene/n-hexane, as well as good recycle stability. This work demonstrates that new DESs can be used as alternative solvents to traditional organic solvents and ionic liquids, and provides ideas for the separation of olefins and paraffins in coker naphtha.

Contamination of groundwater with sulfamethoxazole and antibiotic resistant Escherichia coli in informal settlements in Kisumu, Kenya

High frequency of antibiotic detection in groundwater in informal settlements is attributed to increased usage and improper disposal, thus difficult to identify sources of antibiotic resistance in the environment, worsened by inadequate sanitation facilities and increased population density, particularly in developing-countries. Reliance on groundwater exposes them to pollutants and risk of antibiotic resistance, in addition to experiencing inequities in accessing vital services. Sulfamethoxazole and trimethoprim, used for prophylaxis by HIV/AIDS patients were tested in 49 groundwater sources in Kisumu, Kenya. Only Sulfamethoxazole (SMX) was found, with a detection frequency of 14.3% and concentrations ranging from below limit of quantification (LOQ) to 258.2 ng/L. Trimethoprim (TMP), marketed in combination with sulfamethoxazole, was not detected, owing to its high distribution coefficient (kPa7.12) and, generally, being a bigger molecule with modest water mobility and solubility. Furthermore, TMP ratio in cotrimoxazole is low (5:1), it is expected that mass loading will be lower, as well as influence of the study area’s hydrogeology, where soil is clayey with high porosity and permeability. Escherichia coli was recovered in 98% (n = 48) of water samples, with counts ranging from 16 to 8,850 MPN/100ml. Additionally, resistance to sulfamethoxazole was identified in 6% (n = 3) samples with Inhibition Zone Diameters of 0.8mm(resistant), 10.5mm (resistant), and 11.5mm (intermediate), but not among samples where SMX was detected. Antibiotic concentrations in water that can cause resistance are unknown because antibiotic-resistant E. coli was not found in water samples where sulfamethoxazole was identified, raising concerns about f environmental resistance spread. Concentration of SMX was lower in a previous research, which only collected water from one groundwater source, than the current study, which included additional samples (49). Presence of SMX and Escherichia coli resistance is of concern and necessitates greater attention and regular monitoring for potential contaminants and resistance trigger to avert potential risks to human health.