High Removal Rate Research Articles

Microplastics in an advanced wastewater treatment plant: sustained and robust removal rates unfazed by seasonal variations

Microplastics (MP), fragments of plastic generally defined as, less than 5 mm in size, originating from various urban sources, have become a significant environmental concern due to their widespread presence and potential impacts on ecosystems. This study investigates the efficiency of an advanced wastewater treatment plant discharging into the Mediterranean Sea in removing MPs from wastewater. The plant processes wastewater through a series of treatment stages, including screening, desanding, coagulation/flocculation, biological filtration, and sludge incineration. Samples were collected and analysed during three distinct campaigns (dry, rainy, and touristic seasons) to assess the plant’s performance under varying conditions. Using matrix-representative sampling methodologies and Focal Plane Array micro Fourier-Transform Infrared Spectroscopy (FPA-µFT-IR) for MP quantification, the study measured MP concentrations and removal rates. The treatment plant demonstrated high removal rates of microplastics across different periods. Using a mass balance approach, the removal efficiency during the dry sampling period was 99.85%. In the rainy campaign, the efficiency slightly decreased to 99.11% due to increased runoff, while during the touristic period, the efficiency peaked at 99.95%. Polyester was identified as the predominant polymer type. The primary treatment stages, particularly coagulation/flocculation and lamellar settling, are most effective in MP removal. The majority of MPs are retained in the sludge, which is subsequently incinerated, preventing environmental discharge. This research demonstrates that a WWTP employing advanced treatment processes is not a source of MP to the environment but rather a sink. Despite variations in influent MP concentrations across different seasons, the plant consistently maintained high removal rates, effectively mitigating MP pollution. In this study, sludge incineration further ensured that MPs were prevented from entering the environment.

Pulsed Unipolar-Polarisation Plasma Electrolytic Polishing of Ni-Based Superalloys: A Proof of Conception

The enhanced performance of aerospace equipment drives parts development towards integration, complexity, and structural optimization. This advancement promotes metal near-net fabrication technologies like wire electrical discharge machining (WEDM) and 3D printing. However, the high initial surface roughness from WEDM or 3D printing poses significant challenges for the high-performance surface finishing required. To effectively reduce the surface roughness of the workpieces with high initial surface roughness, this paper proposes pulsed unipolar-polarisation plasma electrolytic polishing (PUP-PEP). The study examined the material removal mechanisms and surface polishing quality of PUP-PEP. This technique combines the high current density and material removal rate of the electrolytic polishing mode with the superior surface polishing quality of PEP through voltage waveform modulation. For an Inconel-718 superalloy part fabricated by WEDM, PUP-PEP reduced surface roughness from Ra 7.39 μm to Ra 0.27 μm in 6 min under optimal conditions. The roughness decreased from Ra 7.39 μm to Ra 0.78 μm in the first 3 min under pulsed unipolar-polarisation voltage, resulting in a remarkable 233% increase in efficiency compared to that with conventional PEP. Subsequently, the voltage output voltage is transformed into a constant voltage mode, and PEP is continued based on PUP-PEP to finally reduce the workpiece surface roughness value to Ra 0.27 μm. The proposed PUP-PEP technology marks the implementation of ‘polishing’ instead of conventional rough-finish machining processes, presenting a new approach to the surface post-processing of metal near-net fabrication technologies.

Advanced oxidation processes by UV/H2O2 for the removal of anionic surfactants in a decentralized wastewater treatment plant in Ecuador

ABSTRACT Surfactants are persistent pollutants that pose risks to ecosystems and human health due to their low removal efficiency in conventional wastewater treatment plants. In Guayaquil, Ecuador, a decentralized facility discharges water with a surfactant concentration that exceeds the national legislation up to 20 times. This work aims to demonstrate the effectiveness of the advanced oxidation process UV/H2O2 in removing anionic surfactants as a tertiary treatment for the decentralized facility investigated. A laboratory-scale batch system was tested for the treatment of real effluent with three hydrogen peroxide concentrations (100, 250, and 500 mg L−1) and UV exposure up to 120 min. All experimental trials were run in duplicate. After 60 min of UV exposure with 250 mg L−1 of H2O2, the anionic surfactant removal was 94.3 ± 4.3%, and the effluent complied with the discharge limits (<0.5 mg L−1). These operational parameters were selected for continuous laboratory-scale experiments to simulate the facility operation, achieving a maximum removal of 92.3 ± 2.5%. Although the reactor demonstrates a high removal rate, improvements to its configuration are necessary to meet discharge limits. The UV/H2O2 process allowed the removal of anionic surfactants, suggesting its feasibility as a complementary treatment in decentralized plants with similar problems.

Trace iron induced piezo-polarization field strength on piezo-promoted peroxymonosulfate activation for pollutant degradation

Advanced oxidation processes based on piezo-promoted peroxymonosulfate (PMS) activation in environmental remediation have been widely applied, but the treatment efficiency of pollutants was restricted by sluggish charge separation and low affinity of PMS. Herein, trace iron-doped layered molybdenum disulfide (Fe/MoS2) was used to degrade pollutants by piezo-promoted PMS activation. Real-time reaction site changes in carbamazepine (CBZ) degradation process were predicted by Fukui function calculation of the reaction intermediates, and the possible degradation pathways were given. Through piezoresponse force microscopy and calculation of the adsorption energy, electronic localized functions and Crystal Orbital Hamilton Population, it was verified that Fe doping improves the adsorption of oxygen-containing reactants on MoS2, enhancing the electron delocalization and piezo-polarization field, thus accelerating the piezo-promoted PMS activation kinetics. The degradation efficiency of CBZ on Fe/MoS2 (0.44 min−1) was about 22 times than that of MoS2. Piezo-promoted PMS activation strategy based on Fe/MoS2 still maintains a high removal rate in the treatment of dye and antibiotic pollutants such as ornidazole, rhodamine B, tetracycline, methyl orange, chlortetracycline. This study provides insights into the mechanism by which piezo-promoted PMS activation, and achieving high chemical efficiency for pollutants removal.

Impact of a care bundle on short peripheral catheter-associated complications in a resource-limited neonatal unit.

Short peripheral catheter (SPC)-associated complications occur frequently in hospitalised neonates. Few studies have reported the use of SPC care bundles in resource-limited neonatal units. To evaluate the impact of a SPC care bundle on SPC associated complications (infiltration, dislodgement, phlebitis) and catheter dwell time. We conducted a quasi-experimental study comparing neonatal SPC complications during a 2-month baseline and a 2-month intervention period, where a SPC care bundle was introduced including hand hygiene, insertion site antisepsis, nurse assistance during cannulation, IV insertion carts and IV securement dressings. A total of 459 SPC days were observed in 223 neonates: 111 pre-intervention and 112 post-intervention (after SPC bundle implementation). Most neonates were preterm (208, 93.3%) with very or extremely low birth weight (133, 59.6%). SPC care bundle compliance was 43.8% for five bundle elements and 83.9% for four bundle elements. Most SPCs had unplanned removal within 48 h of insertion owing to infiltration or dislodgement (89/111 pre-intervention (80.2%) vs 90/112 post-intervention (80.4%); 0.974). No phlebitis was documented. The mean SPC dwell time was unchanged following bundle implementation (32.9 vs 34.2 h; p = 0.376). Infiltration and dislodgement occurred frequently necessitating replacement of four of every five SPCs. Despite moderate compliance with the SPC care bundle, the high rates of unplanned SPC removal and short duration of catheter dwell time were unchanged. The SPC care bundle did not improve catheter dwell time; further research is needed to identify strategies to reduce unplanned SPC removal and extend catheter dwell time in hospitalised neonates.

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.

Bioinspired surface silicification of cellulose-mediated PVDF membranes for significantly enhancing superhydrophilicity and anti-oil adhesion toward ultrafast oil/water emulsion separation

Cellulose is a widely used hydrophilic material due to its rich hydrophilic hydroxyl groups. However, the presence of its lipophilic segment will affect the antifouling performance. Finding strategies to improve this problem has attracted considerable attention. In this work, a layer of silica was applied to a cellulose-deposited polyvinylidene fluoride membrane through a straightforward in-situ bionic silicification process of tetraethyl orthosilicate. The contact angle and oil droplet contact test proved that the high-hydrophilicity and underwater superoleophobicity of the silicified membranes were significantly enhanced. The surface structure and composition were analyzed by scanning electron microscopy, Fourier transform infrared spectroscopy and X-ray photoelectron spectroscopy. The results of show that this improvement was mainly attributed to the presence of silicon hydroxyl groups, buried cellulose chains, and micro-nanostructures composed of cellulose and silica. The stable silica coating also provided protection for the polymeric membrane against degradation after water washing for 24 h, ultrasonic treatment (40 KHZ) for 10 min or exposure to different pH levels (pH=1, 4, 9 and 12) and saturated sodium chloride solution for 24 h. Furthermore, the silicified membrane showed outstanding oil adhesion resistance and permeation flux, enabling effective purification of different oil-in-water emulsions that were stabilized by emulsifiers. Notably, the membrane achieved a high oil removal rate (> 99.4 %) of various emulsions (toluene-in-water, cyclohexane-in-water, tetrachloroethane-in-water, soybean oil-in-water, toluene-in-salt solution, toluene-in-acid solution and toluene-in-alkaline solution emulsions). In particular, for toluene-in-water emulsions (oil droplets in the emulsion ranged from 58.77 nm to 615.1 nm), a significantly enhanced permeation flux (4777 L·m−2·h−1·bar−1) was obtained at 0.8 bar pressure. Even after multiple cycles of separation, the flux was higher than that of the unsilicified membrane. Overall, this approach is mild, simple, efficient, and easily scalable, making it an ideal method for producing superhydrophilic coatings with substantial application potential.

Mechanically durable tri-composite polyamide 6/hematite nanoparticle/tetra-n-butylammonium bromide (PA6/α-Fe2O3/TBAB) nanofiber based membranes for phosphate remediation.

Essential properties for a Point of Use (POU) water filter include maintaining high removal capacity and rate, with excellent mechanical properties to withstand pressure drop. Herein, mechanically robust tri-composite polyamide 6/iron oxide nanoparticles/tetra-n-butylammonium bromide (PA6/α-Fe2O3/TBAB) nanofiber composite membranes were electrospun for phosphate (P) remediation, where the diameter and composition were tuned by controlling solution compositions and electrospinning conditions. Tri-composite composition and morphology affect phosphate uptake where the adsorption capacity followed Langmuir isotherm whereas the adsorption kinetics followed pseudo second order behavior. Mechanical properties (i.e., Young's Modulus (E) and toughness) were significantly influenced by the composition and morphology of the tri-composite, as well. Although additional TBAB and iron oxide decreased toughness, there are optimum composition ranges which resulted in maximum Young's Modulus. Of the synthesized nanofiber membranes, PA6/α-Fe2O3/TBAB nanofibers with 17% α-Fe2O3 and 2% TBAB showed excellent phosphate uptake capacity [i.e., 8.9mg/g (52mg of P/g of α-Fe2O3)] while it is bendable, stretchable, and able to plastically deform without fracturing (i.e., Young's modulus of 2.06 × 108Pa and Toughness of 1.35 × 106Jm-3). With concerns over the impact of P on water resources and the long-term availability of limited P resources, this tri-composite membrane is well suited for applications in both wastewater treatment and resource recovery.

Wastewater-contaminated treatment with heavy metals by using a sustainable green nanomaterial

The current research included treating wastewater with sustainable nanotechnology to remove some trace elements (arsenic, copper, baron, lead, and chromium) by using a nanomaterial extracted from potato plant waste in a sustainable, green, environmentally friendly way, with two different additions, the first adding 0.5 grams and the second adding 1 gram of nanocellulose. For two different periods (6 hours and 12 hours) for both quantities of nanocellulose. The results showed that nanocellulose has a great ability to remove the studied elements from wastewater after comparing their original concentrations that were in the water before treatment with nanocellulose. The results showed that increasing the amount of nanocellulose and increasing the time led to an increase in the removal rate, and this was clear from the results of the statistical analysis, which showed the presence of a positive significant correlation between the rate of removal of trace elements from waste water with increasing the amount of nanocellulose and increasing the time. When comparing the removal rates of the studied elements from wastewater with the PH values, it was found that the pH is the control of these rates, as the highest removal rates were at the neutral or close to acidic level, the pH between 5.5 and 7.5, and when the pH tends towards basicity (8 - 9.5) The removal rate decreased. The results also showed that the removal rate varies between the elements and this depends on the concentration of the element present in the water, its chemical composition, and the degree of its binding to the substance used for treatment.

Facile synthesis of ATTM@ZIF-8 modified pullulan hydrogels for enhanced adsorption of Congo red and malachite green

Efficient capture of dyes from wastewater is of great importance for environmental remediation. Yet constructing adsorbents with satisfactory adsorption efficiency and low cost remains a major challenge. This work reports a simple and scalable method for the fabrication of functionalized porous pullulan hydrogel adsorbent decorated with ATTM@ZIF-8 for the adsorption of congo red (CR) and malachite green (MG). The embedding of ammonium tetrathiomolybdate (ATTM) into the ZIF-8 nanoclusters offered additional adsorption sites and enlarged the pore size of the resulting ATTM@ZIF-8. The homogeneous dispersion of the nanoparticles in the three-dimensional network of polysaccharide gels prevents their agglomeration and thus improves the affinity for dye molecules. The resulting adsorbent AZP-20 at optimized composite ratios exhibits high activity, selectivity, interference resistance, reusability and cytocompatibility in dye adsorption applications, and possesses high removal rate of dye in real water systems. Batch experiments demonstrated that the adsorption rate of AZP-20 for MG and CR was 1645.28 mg g−1 and 680.33 mg g−1, and would be influenced by pH conditions. Adsorption kinetics followed pseudo-second-order model. Adsorption isotherms followed Langmuir model for MG and Freundlich model for CR. The adsorption of dye molecules primarily relied on electrostatic interaction (MG) and π-π stacking interaction (CR). Conclusively, the prepared AZPs adsorbent illuminated good application prospects in the treatment of complex component dye wastewater.

Enhanced cesium removal from wastewater using a potassium hexacyanoferrate/gelatin aerogel composite

In the wake of the 2011 Fukushima nuclear disaster, the presence of radioactive cesium (137Cs) in nuclear wastewater has posed a critical and enduring health risk. Addressing this challenge, we have synthesized a gelatin aerogel, denoted as KCuFC/GA, immobilized with potassium cupric ferrocyanide (KCuFC) through an in situ approach, aiming for the efficient extraction of 137Cs from aqueous environments. This novel aerogel's rich porous structure enhances the accessibility of adsorption sites, thereby significantly promoting the capture of Cs+. The adsorption of cesium onto KCuFC/GA was investigated under various experimental conditions, including initial solution pH, contact time, initial cesium concentration, and the presence of coexisting ions (K+, Na+, Ca2+, Mg2+, Sr2+). The results indicated that the adsorption performance was largely independent of pH, achieving a high cesium removal rate of 93.4 % within the first 5 minutes. The cesium adsorption data were well-described by the Langmuir adsorption model, indicating a maximum adsorption capacity of 222.22 mg·L−1. Furthermore, in the presence of various competing ions, KCuFC/GA has demonstrated unparalleled selectivity for Cs+, with a partition coefficient (Kd) of 2.49 × 105 mL·g−1, and has sustained its adsorptive properties across five cycles of use. Through systematic investigation, including X-ray photoelectron spectroscopy (XPS) analysis, we have elucidated the adsorption mechanism, highlighting the pivotal role of ion exchange between lattice K+ and Cs+. The straightforward fabrication process and the aerogel's robust cesium removal capabilities from complex solutions indicate that KCuFC/GA is a promising candidate for real-world applications in the treatment of radioactive wastewater.

Enhancing Fenton-like reaction mediating performance of covalent organic frameworks through porosity modification

Covalent organic framework (COF) catalytic photocatalysts mediating Fenton-like reactions have been applied to the treatment of organic dyes in printing and dyeing wastewater. However, the photocatalytic performance of original COF is often unsatisfactory. This study investigated the impact of porosity modification strategies on the performance of COF photocatalysts in mediating the removal of organic dyes via Fenton-like reaction. Porosity modification was achieved by increasing the concentration of acetic acid (HAc) catalyst during COF preparation. The modified TAPB-DMTA COF (12M COF) exhibited excellent adsorption and photocatalytic properties. The Fenton-like reaction mediated by 12M COF photocatalysis removed nearly 96% of malachite green (MG) within 20 min, with a rate constant of 0.091 min−1, which was 2.9 and 6.5 times higher than that of g-C3N4 and original COF under the same reaction conditions, respectively. Additionally, the modulation mechanism of porosity modification on COF photocatalysis was explored. The conduction band (CB) of COF was reduced from −0.14 eV to −0.38 eV after porosity modification, facilitating the generation of longer-lived O2•- in the reaction system, which was conducive to efficient MG removal. Anti-interference experiments showed that the photocatalytic Fenton-like reaction system based on 12 M COF was less affected by common anions, cations and dissolved organics, while maintaining a high MG removal rate in tap water, mid-water, secondary clarifier effluent and river water. In summary, porosity modification was an effective strategy to improve the catalytic performance of original COFs. This study presented an efficient metal-free photocatalyst modification strategy for the Fenton-like reaction while avoiding the production of toxic by-products during dye degradation.

UDP-glycosyltransferase UGT96C10 functions as a novel detoxification factor for conjugating the activated dinitrotoluene sulfonate in switchgrass.

Dinitrotoluene sulfonates (DNTSes) are highly toxic hazards regulated by the Resource Conservation and Recovery Act (RCRA) in the United States. The trinitrotoluene (TNT) red water formed during the TNT purification process consists mainly of DNTSes. Certain plants, including switchgrass, reed and alfalfa, can detoxify low concentrations of DNTS in TNT red water-contaminated soils. However, the precise mechanism by which these plants detoxify DNTS remains unknown. In order to aid in the development of phytoremediation resources with high DNTS removal rates, we identified and characterized 1-hydroxymethyl-2,4-dinitrobenzene sulfonic acid (HMDNBS) and its glycosylated product HMDNBS O-glucoside as the degradation products of 2,4-DNT-3-SO3Na, the major isoform of DNTS in TNT red water-contaminated soils, in switchgrass via LC-MS/MS- and NMR-based metabolite analyses. Transcriptomic analysis revealed that 15 UDP-glycosyltransferase genes were dramatically upregulated in switchgrass plants following 2,4-DNT-3-SO3Na treatment. We expressed, purified and assayed the activity of recombinant UGT proteins in vitro and identified PvUGT96C10 as the enzyme responsible for the glycosylation of HMDNBS in switchgrass. Overexpression of PvUGT96C10 in switchgrass significantly alleviated 2,4-DNT-3-SO3Na-induced plant growth inhibition. Notably, PvUGT96C10-overexpressing transgenic switchgrass plants removed 83.1% of 2,4-DNT-3-SO3Na in liquid medium after 28 days, representing a 3.2-fold higher removal rate than that of control plants. This work clarifies the DNTS detoxification mechanism in plants for the first time, suggesting that PvUGT96C10 is crucial for DNTS degradation. Our results indicate that PvUGT96C10-overexpressing plants may hold great potential for the phytoremediation of TNT red water-contaminated soils.

Chemical-mechanical synergetic effect of single crystal SiC polishing using Fe3O4@MIL-100(Fe) magnetic photo-Fenton catalyst

Achieving an atomically smooth surface on single-crystal silicon carbide (SiC) with a high material removal rate (MRR) is challenging. Traditional chemical mechanical polishing (CMP) often uses aggressive slurries that are inefficient and environmentally hazardous. To address these challenges, we synthesized a novel core-shell structure Fe3O4@MIL-100(Fe) magnetic catalyst and utilized it as a non-homogeneous photo-Fenton catalyst in friction wear tests on SiC wafers within a simulated CMP environment. The catalyst was thoroughly characterized using X-ray diffractometry (XRD), scanning electron microscopy (SEM), and X-ray photoelectron spectroscopy (XPS). Additionally, we explored the effects of various components, pH levels, H2O2 concentrations, catalyst concentrations, and light intensities on the friction wear of SiC wafers. The results indicate that, under visible light conditions, Fe3O4@MIL-100(Fe) exhibits a strong Fenton catalytic effect, achieving a maximum material removal rate of 61.076*103μm3/min at a pH of 3, H2O2 concentration of 5 wt%, catalyst concentration of 14 g/L, and light intensity of 500 W. These findings provide valuable theoretical support for visible light assisted catalyzed CMP of SiC.

Ti3C2TX MXene/loofah-derived carbon aerogel for high-efficiency adsorption of organic pollutants in wastewater

The contamination of wastewater by organic pollutants significantly impacts human health and the environment due to their carcinogenic nature and various adverse effects. To address this issue, this study offers a high-efficiency and low-cost biomass-based carbon aerogel adsorbent, which was prepared through the hydrothermal carbonization of loofah, followed by Ti3C2TX MXene impregnation. The aerogel features a porous three-dimensional network structure and a substantial specific surface area, facilitating broad-spectrum adsorption capabilities for various dyes and drugs. The aerogel achieved impressive adsorption capacities of 175.29 and 75.73 mg/g for cationic methylene blue and Rhodamine B dyes, and 106.33 and 93.29 mg/g for anionic methyl orange and Congo red dyes, as well as 86.25 mg/g for tetracycline hydrochloride, surpassing other reported biomass-based aerogels. Furthermore, it demonstrated effective decolorization ability for wastewater containing mixed dyes. Notably, it exhibited excellent recycling and regeneration properties, maintaining a high removal rate after multiple cycles of adsorption–desorption. The adsorption process of dye/drug by the aerogel followed Langmuir’s monomolecular layer adsorption model, exhibiting spontaneous, endothermic, and disorder-increasing behavior in alignment with the pseudo-second-order kinetic model. This study presents an efficient biomass-based aerogel for the removal of organic pollutants from wastewater.

Efficient removal of chlortetracycline hydrochloride and doxycycline hydrochloride from aqueous solution by ZIF-67

ZIF-67 nanoparticles were synthesized by a simple method at room temperature and used to remove chlortetracycline hydrochloride (CTC) and doxycycline hydrochloride (DOX) from water. ZIF-67 was characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), fourier transform infrared spectroscopy (FT-IR), Brunauer-Emmett-Teller (BET) surface area, X-ray photoelectron spectroscopy (XPS), thermogravimetry (TGA) and zeta potential analyzer. The morphology and chemical composition of the synthesized ZIF-67 were characterized. The effects of key parameters such as pH, dosage, temperature, contact time, different initial concentrations and coexisting ions on the adsorption behavior were systematically studied. The results of batch adsorption experiments indicate that the adsorption process conforms to the pseudo-second-order kinetic model and Sips model. At 303K, the removal rates of CTC and DOX at 150 mg/L reached 99.16 % and 97.61 %, and the maximum adsorption capacity of CTC and DOX reached 1411.68 and 1073.28 mg/g, respectively. At the same time, ZIF-67 has excellent stability and reusability. Most importantly, the possible adsorption mechanism is proposed by exploring the changes of SEM, TEM, BET and FT-IR characterization results before and after the reaction, which mainly includes pore filling, electrostatic interaction and π-π interaction. The prepared ZIF-67 has a large specific surface area (1495.967 m2 g−1), achieves a high removal rate within a short time frame, and maintains a high removal rate across a wide pH range. These characteristics make ZIF-67 a potentially promising adsorbent for removing antibiotics from aqueous solutions.

Examining the Stability and Durability of Child Care Arrangements during the COVID-19 Pandemic in Canada

La pandémie de COVID-19 a provoqué d'importantes perturbations dans tous les secteurs du travail et de la vie familiale, y compris les services de garde éducatifs à l'enfance (SGÉE). Les recherches démontrent que l'instabilité (soit les interruptions aux services de garde) et l'absence de durabilité des SGÉE (soit le maintien des mêmes services de garde au fil du temps) peuvent exacerber le stress des parents et nuire au développement de l'enfant. S'inspirant des données d'un sondage original réalisé en décembre 2020 auprès de 882 parents de jeunes enfants de quatre provinces canadiennes, les autrices ont examiné les choix des parents au sujet de la garde d'enfants avant la pandémie et les répercussions de la COVID-19 sur ces dispositions, dans l'immédiat et à long terme. Dans leur échantillon, elles ont trouvé que a) les services hors du domicile étaient plus instables et plutôt moins durables que ceux à domicile; b) la perte d'accès pendant la pandémie à cause de la fermeture des centres de la petite enfance était moins marquée en Colombie-Britannique, ce qui était toutefois contrebalancé par un taux relativement élevé de retraits volontaires; c) l'Ontario a présenté un taux relativement élevé de pertes d'accès en raison des fermetures et des retraits volontaires; d) dans l'ensemble, 64 % des dispositions en matière de garde se sont révélées durables, mais e) la durabilité était plus faible dans les familles à plus faible revenu et en Ontario. En revanche, la durabilité était beaucoup plus élevée au Québec, ce qui fait ressortir le rôle possible des investissements dans les politiques des SGÉE pour protéger les parents et les enfants en cas d’événements déstabilisants.

Dielectric Fluids for the Electrical Discharge Machining: A Review

An extensive examination of the effect of dielectric properties of the Electrical Discharge Machining (EDM) operation machining variables is being done in the present study. Irrespective of the material's hardness, an EDM is an unconventional thermo-erosion machining procedure. It gave the workpiece a better and more detailed surface topography. Dielectric is an essential EDM component that typically affects the operation's high material removal rate and surface integrity. The dielectric fluid acts as a medium that modulates electrical sparks and traps energy due to the operation. It cleans up the trash and cools the workpiece. Whenever powders like Ti, Si, graphite, Cu, Al2O3, and others are added to the dielectric fluid, the fluid's conductivity increases the micro-hardness of the substance. For executing studies in EDM, choosing a proper dielectric from the number of fluids now offered is crucial. Adopting different additives in the dielectric fluid impacts the optimization of machining parameters and related characteristics are addressed in this study in light of existing research. The studies show the effect on various output parameters.

Highly effective and selective recovery of germanium from coal acid leaching solution by trihydroxyl functionalized titanium dioxide

In this study, a novel trihydroxyl functionalized titanium dioxide (TiO2-NH2-3OH) was successfully synthesized by the Schiff base reaction method. TiO2-NH2-3OH was characterized by Scanning Electron Microscopy (SEM), Fourier Transform Infrared Spectroscopy (FT-IR), x-ray Photoelectron Spectroscopy (XPS), x-ray diffraction techniques (XRD), and further applied to recover germanium (Ge(IV)) from coal acid leaching solution. TiO2-NH2-3OH exhibited superior capture performance on Ge(IV) at a pH of 3, and the optimal TiO2-NH2-3OH dosages were 0.8 g L−1. The distribution coefficients of germanium for coexisting metal ions (Zn2+, Co2+, Mn2+, Ni2+ and Al3+) were all greater than 1, indicating that TiO2-NH2-3OH had good selective adsorption performance for Ge(IV) in complex solution environments. Compared with other kinetic models, pseudo-second-order model was more suitable to reveal the absorption of Ge(IV). Moreover, the experiment data were fitted better with Langmuir model at 298 K than the other isothermal models, and the maximum adsorption capacity was up to 72.94 mg g−1. Thermodynamic data suggesting that the capture of Ge(IV) on TiO2-NH2-3OH was a spontaneous endothermic process, increasing the temperature was beneficial for the adsorption reaction to proceed. TiO2-NH2-3OH with saturated adsorption still maintained a high removal rate of 80.55 % of Ge(IV) after five cycles, indicating good stability and recyclability of TiO2-NH2-3OH. XPS analysis indicated that the capture of germanium by TiO2-NH2-3OH may be due to the ion exchange interaction between -OH and Ge(OH)4 on the adsorbent surface. This work indicated that TiO2-NH2-3OH had great advantages and potential for the recovery of Ge(IV) from coal acid leaching solution.

Efficient removal of environmentally hazardous heavy metal ions from water by NH2-MIL-101-Fe and MOF-808-EDTA based polyether sulfone adsorbents

The potential of metal–organic frameworks (MOFs) based polymeric composites for heavy metal removal was analyzed in this study. Two mixed matrix composites, along with NH2-MIL-101-Fe and MOF-808-EDTA, were synthesized. The MOFs were synthesized using the solvothermal method, and the mixed matrix spheres (MMSs) were prepared using the facile dropping method. The MMSs were characterized, and batch adsorption studies were performed at different pH and adsorbent dosages. For both MMSs, the optimum pH was between 5–5.5, and the highest removal rates were obtained for MOF-808-EDTA spheres (94 % Hg2+, 86 % As, 80 % Mn). The optimum adsorbent dosage for MOF-808-EDTA was found to be 5.42 g/L, while for NH2-MIL-101-Fe, it was 7.13 g/L, after which the metal ion removal efficiency was reduced. Langmuir adsorption isotherm was fitted with thermodynamic evaluation of Gibbs free energy, enthalpy, and entropy. MOF-808-EDTA demonstrated a greater adsorption capacity of 272.7 mg/g (Hg2+), 151.29 mg/g (As3+), and 125.9 mg/g (Mn2+) than the other MMP. The Gibbs free energy of −20.14 (Hg2+), −12.66 (Mn2+), and −52.61 kJ/mol (As3+) were obtained from the thermodynamic study. The results indicated that the process was exothermic and spontaneous. Breakthrough column studies were performed for MOF-808-EDTA spheres using the pore-surface-diffusion model. The transient column study was conducted for individual heavy metal ion solutions using Addesign™ software to evaluate column exhaustion time, breakthrough time and length of mass transfer zone. Studies with multicomponent solutions of heavy metals also gave potentially promising results in the separation of 92 % of Hg, 84 % As, and 75 % Mn which indicates the prepared adsorbents can be used to remove heavy metal ions from industrial wastewater samples.