La (NO3)3 substantially fortified Glycyrrhiza uralensis's resilience against salt stress by interconnected pathways.

The taproot of Glycyrrhiza uralensis is globally appreciated for its medicinal and commercial value and is one of the most popular medicinal plants. With the decline of wild G. uralensis resources, cultivated G. uralensis has become a key method to ensure supply. However, soil salinization poses challenges to G. uralensis cultivation and affects the yield and quality of it. In this study, the inhibitory effects of NaCl and Na2SO4 on yield and quality of G. uralensis were comprehensively evaluated in a three-year large-scale pot experiment, and the alleviating effects of supplementation with lanthanum nitrate (La (NO3)3) on G. uralensis were further evaluated under salt stress. The findings indicate that La (NO3)3 significantly strengthened the plant's salt tolerance by enhancing photosynthetic capacity, osmolyte accumulation, antioxidant defenses, and cellular balance of ions, which led to a substantial increase in root biomass and accumulation of major medicinal components. In comparison to the NaCl-stress treatment, the 0.75 M La (NO3)3 + NaCl treatment resulted in a 20% and 34% increase in taproot length and biomass, respectively, alongside a 52% and 43% rise in glycyrrhizic acid and glycyrrhizin content, respectively. Similar improvements were observed with 0.75 M La (NO3)3 + Na2SO4 treatment, which increased root length and biomass by 14% and 26%, respectively, and glycyrrhizic acid and glycyrrhizin content by 40% and 38%, respectively. The combined showed that application of La (NO3)3 not only significantly improved the salt resilience of G. uralensis, but also had a more pronounced alleviation of growth inhibition induced by NaCl compared to Na2SO4 stress except in the gas exchange parameters and root growth. This study provides a scientific basis for high-yield and high-quality cultivation of G. uralensis in saline soils and a new approach for other medicinal plants to improve their salt tolerance.

Time-Dependent Hydrothermal Synthesis of La2O3 NPs for Effective Catalytic Activity of Ionic Dye.

Lanthanum oxide was successfully synthesized by hydrothermal method by varying the reaction time such as 6, 12, and 24 h. In XRD, study confirms the presence of a hexagonal structure, and the phase remains the same at different times; the main goal is to assess the average crystallite size of prepared La2O3 nanoparticles, which was found in the range of 6 to 8 nm. An interesting observation from the XRD data was the apparent increase in crystalline nature as the synthesis time was extended. The UV-Vis spectroscopic studies show a change in the band gap when the reaction time is changed. The morphology analysis shows that the image revealed that the particles formed were agglomerated and formed a spherical shape, with diameters ranging between 35 and 86 nm. When tested for photocatalytic activity, the La2O3 nanoparticles show a degradation of methylene blue dye when the time varies. Remarkably, the nanoparticles synthesized exhibited a profound ability to degrade the dye, with an efficiency rate hitting as high as 89% under halogen light illumination.

Enhanced aqueous phosphorus removal and mechanism by water spinach (Ipomoea aquatica Forsk) pretreated with lanthanum nitrate.

Excess nutrients such as phosphate (PO43-) entering surface waters promote eutrophication, and phosphorous (P) removal is important to clear the water. Phytoremediation efforts have been used to improve water quality by varieties of P removal plants, such as water spinach (Ipomoea aquatica Forsk). Water spinach can reduce both internal and external resources of phosphorus from waterbody. The ion of lanthanum (La), one rare earth element (REE), is an immobilization substance for aqueous phosphate and also a fertilizer for plants. Therefore, lanthanum nitrate La (NO3)3 was used further to improve the phytoextraction of P from the polluted water. This study investigated the effects of La on the aqueous P removal by two genotypes of water spinach, green stem large leaves (GSLL) and green stem willow leaves (GSWL). The low concentration La (NO3)3 helped the plant to remove more phosphorous from eutrophic water, but La at high concentration lowered the removal of P. Under La (NO3)3 treatments, the optimum concentration for maximum P removal in GSLL is 3 mg/L, and for GSWL, it is 10 mg/L and P removal rates were enhanced to 95% and 96%, respectively. When the concentration of La (NO3)3 is 100 mg/L, the removal percentage of P was only 10% for both genotypes. The very high concentration of La will impose toxicity and even cause the death of the water spinach and produce secondary pollution; for example, under some specific circumstances, the bond between lanthanum and nitrates dissociates into lanthanum ions (La3⁺) and nitrate ions (NO3⁻). If the concentration is high, then it accumulates in the aquatic water organisms and plants and causes toxicity in their bodies. If humans eat up these plants and fish, it causes toxic effects in humans. The La (NO3)3 positively affects different parameters of plants. La (NO3)3 increases the growth, pigments, enzyme activity, and malondialdehyde (MDA) of plants which were also discussed in this study. The biological mechanism should be responsible for the enhanced aqueous phosphorus removal by water spinach using lanthanum nitrate.

Synthesis and characterization of Lanthanum Oxide nanoparticles using Citrus aurantium and their effects on Citrus limon Germination and Callogenesis.

The plant extract-mediated method is eco-friendly, simple, safe, and low-cost, using biomolecules as a reducing agent to separate nanoparticles. Lanthanum (La) is a rare earth metal that positively affects plant growth and agriculture. Citrus limon is a leading citrus fruit with many varieties. Conventional vegetative propagation methods depend on season, availability of plant material and are time-consuming. It is the main reason for limiting the acceptance of new varieties. So, In-vitro propagation of the lemon method is practiced overcoming all these problems. Lanthanum oxide nanoparticles (La2O3-NPs) were synthesized using plant extract of C. aurantium. Ultraviolet (UV)-Visible Spectroscopy, Scanning Electron Microscopy (SEM), Transmission Electron Microscopy (TEM), Fourier Transform Infrared (FTIR) spectroscopy, and Thermal Gravimetric Analysis (TGA) were used to characterize the synthesized La2O3-NPs. Fabricated La2O3-NPs were oval and spherical, with an average size of 51.1 nm. UV-visible absorption spectra of La2O3-NPs were shown at a sharp single peak at 342 nm and FTIR showed stretching frequency at 455 cm-1-516 cm-1. In the TGA outcome, mass loss was 9.1%. In vitro experiments demonstrated that La2O3-NPs significantly enhanced the germination and growth of C. limon seeds, achieving an 83% germination rate at 5 mg/L concentration, with uncoated seeds showing root initiation at 10 days and shoot formation at 15 days. Furthermore, La2O3-NPs effectively stimulated callus induction and maturation, with optimal responses observed in media containing MS and 2 mg/L 2,4-D, resulting in a maximum callus frequency of 100% from leaves and 87.5% from shoots at 5 mg/L concentration. These findings underscore the potential of La2O3-NPs to improve seed germination rates, seedling vigor, and callogenesis efficiency, suggesting their promising integration into agricultural practices for sustainable crop production, especially in suboptimal growing conditions. Future research is recommended to explore the mechanisms and broader applications of La2O3-NPs across various plant species and environments.

Metabolomics reveals the potential mechanism of La(III) promoting enrichment of Sodium hydrogen arsenate and Roxarsone in Solanum nigrum L.

The rare earth element lanthanum (La(III)) has been found to effectively enhance crop yields and improve plant growth and development. Arsenic (As), as a class of toxic metals widely found in the environment, poses a serious threat to both ecological and human health. Research on the application of La(III) in phytoremediation to enhance remediation efficiency is currently lacking. This study examined the impact of La(III) on physiological and biochemical indicators of Solanum nigrum L. (S. nigrum) exposed to Sodium hydrogen arsenate (SA) and Roxarsone (ROX) treatments under hydroponic conditions. Results indicated that La(III) treatment increased S. nigrum's aboveground As transport capacity by 58.68 %-213 % compared to no La(III) application. Additionally, foliar spraying of La(III) significantly inhibited the expression of toxic metabolites in the root system of S. nigrum, reducing Benzamide by 99.79 % under SA treatment and ZON by 87.72 % under ROX treatment. La(III) is likely to promote the transport of toxins and nutrients within and out of cells by activating ABC transporters, thereby enhancing S. nigrum's arsenic tolerance and metabolic activity. These findings provide molecular-scale insights into La(III) enhancement of the resilience of hyper-enriched plants and the remediation potential of contaminated sites.

Lanthanum(III)-amino acid chelate mitigates copper(II) stress in rice (Oryza sativa).

Lanthanum (La(III)) is recognized for its ability to mitigate heavy metal stress in plants. However, the inorganic La(III) salts and lanthanum oxide nanoparticles (La2O3 NPs) extensively used in agriculture are prone to soil immobilization, thereby compromising their bioavailability and posing environmental risks. This study synthesized and characterized the lanthanum(III)-amino acid chelate (La(III)-AA) from soybean protein isolate (SPI) hydrolysates. Maximum chelating rate (94.95%) was achieved under the conditions of mole ratio 1:1.5, pH 8.0, 50 ℃ and 5 h. Glu, Asp and Pro represent the primary La(III)-binding ligands. UV-vis and FTIR demonstrated that amino nitrogen and carboxyl oxygen participate in metal-ligand recognition. Scanning and Transmission electron microscopy showed that La(III) chelates with amino acids in a core-shell structure of uniform size. Consequently, a proposed chemical structure for the La(III)-AA complex was presented. A concentration of 20 mg/L La(III)-AA outperforms inorganic La salts in growth promotion and Cu detoxification. La(III)-AA significantly reduces the content of Cu (II) in rice tissues and enhances seedling tolerance to Cu (II) stress. This study provides a novel La(III)-based candidate for crop protection and furthers our understanding of rare earth element-induced mitigation of heavy metal stress.

Chitosan-amidated lignin aerogel beads efficiently loaded with lanthanum hydroxide for phosphate removal from aqueous solutions.

Developing phosphorus removal adsorbents with high adsorption performance and excellent structural stability remains a challenge. Herein, a chitosan (CS) - amidated lignin (AL) gel-bead adsorbent with high efficiency in immobilizing lanthanum hydroxide (La(OH)3) was fabricated via an in situ precipitation and freeze-drying strategy (abbreviated as La@ALCSx). The abundant hydroxyl and amino groups in CS promoted excellent loading of La(OH)3 on the surface and inside of the adsorbent. The introduction of lignin enhanced the structural stability of the beads along with the mass transfer efficiency. Owing to the porous structure and high La utilization, the adsorption capacity of La@ALCS2 reached 130.52 mg P g-1. Intra-sphere complexation of La(OH)3 with phosphate resulted in high adsorption selectivity of La@ALCS2. Moreover, the millimeter-sized of La@ALCS2 has favourable recoverability and maintains high adsorption performance after five adsorption-desorption cycles. Characterization analysis indicated that electrostatic attraction and ligand exchange were the main adsorption mechanisms. The excellent phosphorus removal efficiency, separation efficiency and recyclability of La@ALCSx provide a viable solution for the remediation of phosphate contaminated waters.

Natural organic matter (NOM) can increase the uptake fluxes of three critical metals (Ga, La, Pt) in a unicellular green alga.

Critical metals such as gallium, lanthanum and platinum are considered essential in a modern economy and for the required energy transition. Their relatively recent and increasing use in new technologies have led to an increase in their environmental mobility. As they reach aquatic systems, these metals can interact with organic ligands and especially Natural Organic Matter (NOM). The formation of organic complexes would be expected to reduce metal bioavailability and uptake by living cells, according to the Biotic Ligand Model (BLM). However, exceptions to this model have been determined for several critical metals in the past. The present work compared internalization kinetics of Ga, La and Pt in the green alga Chlamydomonas reinhardtii in the presence of NOMs from different origins: humic and fulvic acids from Suwannee River as well as NOMs from Ontario (Bannister Lake and Luther Marsh). Complexation was determined using a partial ultrafiltration method allowing for a normalization of data based on speciation to compare all conditions based on the concentration of the metal that was not bound to NOM. While internalization metal fluxes varied greatly from one NOM source to the other, uptake was almost always significantly higher than expected based on metal speciation. Quite often, metal internalization fluxes were even significantly increased in the presence of NOM, for the same total metal exposure concentration. For instance, Pt internalization was twice greater in the presence of Bannister Lake NOM than it was in the absence of NOM. The assumption that such exceptions could be explained by NOM characteristics was contradicted by the variable results from one metal to another. To further explore this phenomenon, internalization mechanisms for these individual metals need to be elucidated. This is a necessary step to accurately estimate the risk posed by the presence of these metals in humic aquatic systems.

Great truths are always simple: A millimeter-sized macroscopic lanthanum-calcium dual crosslinked carboxymethyl chitosan aerogel bead as a promising adsorbent for scavenging oxytetracycline from wastewater.

Given their increasing environmental and health harms, it is crucial to develop green and sustainable techniques for scavenging antibiotics represented by oxytetracycline (OTC) from wastewater. In the present work, a structurally simple lanthanum-calcium dual crosslinked carboxymethyl chitosan (CMCS-La3+-Ca2+) aerogel was innovatively synthesized for adsorptive removal of OTC. It was found that CMCS and La3+ sites collaboratively participated in OTC elimination, and OTC removal peaked over the wide pH range of 4-7. The process of OTC sorption was better described by the pseudo-second-order kinetic model and Redlich-Peterson model, and the saturated uptake amount toward OTC was up to 580.91 mg/g at 303 K, which was comparable to the bulk of previous records. The as-fabricated composite also exerted exceptional capture capacity toward OTC in consecutive adsorption-desorption runs and high-salinity wastewater. Amazingly, its packed column continuously ran for over 60 h with a dynamic uptake amount of 215.21 mg/g until the adsorption was saturated, illustrating its great potential in scale-up applications. Mechanism studies demonstrated that multifarious spatially-isolated reactive sites of CMCS-La3+-Ca2+ cooperatively involved in OTC capture via multi-mechanisms, such as n-π EDA interaction, H-bonding, La3+-complexation, and cation-π bonding. All the above superiorities endow it as a promising adsorbent for OTC-containing wastewater decontamination.

Electrochemical Determination of Dopamine with a Carbon Paste-Lanthanum (III) Oxide Micro-Composite Electrode: Effect of Cetyl Trimethyl Ammonium Bromide Surfactanton Selectivity.

This paper presents a new application of a lanthanum oxide (III)-modified carbon paste electrode (LaOX/CPE) for dopamine (DP) detection in the presence of ascorbic acid (AA). The presence of cetyl trimethyl ammonium bromide (CTAB) facilitated the LaOX/CPE electrode's ability to detect DP amidst AA interference, resulting in a substantial 70.0% increase in the anodic peak current for DP when compared to the unmodified carbon paste electrode (CPE). CTAB enabled clear separation of the anodic peaks for DP and AA by nearly 0.2 V, despite their initially overlapping potential values, through the ion-dipole interaction of AA and CTAB. The electrode was characterized using cyclic voltammetry (CV) and energy-dispersive spectroscopy (EDS). The method demonstrated a detection limit of 0.06 µmol/L with a relative standard deviation (RSD) of 6.0% (n = 15). Accuracy was assessed through the relative error and recovery percent, using urine samples spiked with known quantities of DP.

Catalytic wet air oxidation removal of tetracycline by La2O3 immobilized on recycled polyethylene terephthalate using the response surface methodology.

This study investigated the removal of tetracycline from the aqueous solutions by lanthanum oxide nanoparticles covered with polyethylene terephthalate (PET) using a low-cost and facile co-precipitation method, via catalytic wet air oxidation process (CWAO) by response surface methodology (RSM). XRD, FTIR, SEM, and EDX-map techniques have been employed to investigate the crystal structure, functional groups on the surface, morphologic characteristics, and elemental composition, respectively. Under optimum conditions (pH= 9, initial TC concentration= 20 mg L-1, nanocomposite dosage= 1.5 g L-1, pressure= 4 bar, temperature= 70 °C, and time= 90 min), TC removal efficiency by La2O3-PET was achieved at about 99.9%. The environmental parameters were assessed to determine tetracycline catalytic wet air oxidation degradation rate, which included cleaning gases, hydrogen peroxide, type of organic compounds, anions, radical scavenger and reusability. The ANOVA results indicated that the polynomial model proves that the model is entirely meaningful (F-value> 0.001 and P-value< 0.0001) and has high coefficient values of adjusted R2 (0.7404) and predicted R2 (0.5940). The findings indicated that the variables of time, pH, temperature, dosage, and TC concentration have the greatest role in removing tetracycline, respectively. However, pressure as a factor does not have a considerable influence on the performance of the system. In general, due to the presence of the role of additional anionics, the effectiveness of this method for removing tetracycline from drinking water was 82.76%. The catalyst indicated pleasing stability and recycling power during eight testing cycles. Further, the estimated electrical energy per order consumption (EEO) for the CWAO/La2O3-PET system was calculated as 5.31 kWh m-3 with an operational cost (OC) utilization of 1.78 USD kg-1 and it has been shown that this process is feasible and economically comparable to other CWAO processes. The breakdown intermediate products of tetracycline in the CWAO were examined using gas chromatography/mass spectrometry (GC-MS) analysis. The toxicity analyses for the removal of TC were carried out using Daphnia magna and the CWAO process achieved a remarkable decrease in the presence of La2O3-PET nanocomposite (LC50 and toxicity unit (TU) 48 h equal to 0.634 and 157.72 vol percent).

Construction of La1-xSrxNiO3/g-C3N4 type-Z heterojunctions with enhanced visible-light photocatalytic degradation of organic pollutants.

Lanthanum nickelate (LaNiO3), known for its high visible-light absorption, is a promising photocatalyst for water purification. However, the low conduction band position and high photogenerated carrier complexation rate of pure LaNiO3 limit its photocatalytic activity. To address this issue, we investigated the synergistic effects of doping and constructing heterojunctions. A La0.9Sr0.1NiO3 (20%)/g-C3N4 (L2CN8) heterojunction was successfully created. In addition, various characterisation techniques were then employed to analyse the structure-performance relationships of these heterojunction photocatalysts in degrading organic dyes. Results revealed that at a 10% Sr doping level, the oxygen vacancy content was 0.68, which is significantly higher than that of LaNiO3 (0.05). The increased number of oxygen vacancies enhanced the electron capture ability and improved the separation efficiency of photogenerated carriers. Furthermore, the optimised L2CN8 (20 mg) achieved 81.2% and 73.8% removal of methylene blue (50.0 mL, 10 mg L-1) and tetracycline (50.0 mL, 10 mg L-1) under simulated visible-light irradiation (λ > 420 nm). Furthermore, an active species capture experiment confirmed the significant role of superoxide radicals (·O2-) in the degradation process. Based on these experimental findings, we proposed a rational Z-type charge transfer mechanism. This study holds great importance for water pollution control and environmental protection.

Lanthanum hydroxide@cellulose membranes with tunable pore sizes for selective removal of dyes with the same charges.

Adsorptive membranes for the efficient separation of dyes with the same charges are quite desirable. Herein, a novel membrane of lanthanum hydroxide/cellulose hydrogel coated filter paper (LC) was prepared through a facile strategy of dip-coating followed by freeze-shaping. With the aid of cellulose gel, the generated La(OH)3 achieved fine dispersion. In addition, the pore size of LC membrane could be regulated by altering the cellulose concentration or the lanthanum chloride dosage, which was crucial for its water flux. In particular, the obtained membrane possessed a high water flux (128.4 L m-2 h-1) and a high dye rejection (97.2 %) for anionic Congo red (CR) only driven by the gravity, which outperformed many previously reported membranes. More intriguingly, its dye rejection for anionic methyl orange (MO) was only 0.9 %, exhibiting high selectivity for dyes with the same charges. Single-solute adsorption experiments indicated that the CR adsorption on the membrane was best fitted by the pseudo-first-order kinetic model, and it followed the Langmuir monolayer adsorption mechanism.

Combining effects of submerged macrophytes and lanthanum-modified bentonite on sediment enzyme activity: Evidence from mesocosm study.

Lanthanum-modified bentonite (LMB) combined with submerged macrophytes (SM) has been a conventional means of eutrophication management in lakes in recent years, and is one of the most important methods for P removal. However, trends in nutrients and sediment enzymes at the water-sediment interface during this process have not been systematically assessed, and there are still some gaps in how abiotic properties drive changes in enzyme activity. Here, we show changes in aquatic environmental conditions under the action of different ratios of modified bentonite (0, 10%, 20%, and 30%) in combination with SM (Vallisneria natans, Potamogeton lucens, and Hydrilla verticillate) and quantify their effects on sediment enzyme activities. The results showed that the nutrient cycling at the water-sediment interface was facilitated by the combined effect of SM and LMB, which effectively reduced the overlying water nutrient concentration, increased the sediment enzyme activity and enhanced the N cycling process. Partial least squares structural equation model (PLS-SEM) showed that sediment parameters strongly influenced changes in enzyme activity, with NO3-N as the main controlling factors. Our study fills in the process of changing environmental conditions in lake water under geoengineered materials combined with macrophyte measures, especially the changes in biological properties enzyme activities, which contributes to a clearer understanding of nutrient fluxes during the management of eutrophication in lakes.

Reutilization of post-adsorption lanthanum-loaded straw alleviates phosphorus pollution in rice-wheat system: Subsequent performance and underlying mechanisms.

Adsorption technology for phosphorus (P) removal is considered promising and reutilization of post-adsorbent can contribute to promoting sustainable agricultural production. However, the long-lasting impact of the post-adsorbent on crop growth and P remains unclear. This study assessed the effects of P-adsorbed lanthanum-modified straw (La@straw-P) on the rice yield, P fractionation and associated water quality parameters. The findings indicated that, compared with traditional fertilizer regimes, La@straw-P expedited the P reduction in the flooding water achieving a rate of decline to the tertiary standard for surface water (0.20 mg/L) 3.8 times faster and enhanced increased the P harvest index by 17.00 %. Economic estimation proved the positive benefits of La@straw-P in planting-breeding combination system. Redundancy analysis (RDA) and co-occurrence network analysis (CONA) revealed that electrical conductivity (EC) and dissolved Fe played primary roles in regulating total P. Fourier transform infrared spectra (FTIR), X-ray diffraction (XRD), X-ray photoelectron spectra (XPS), and soil P fractions collectively demonstrated that the abundant adsorption sites on La@straw-P could facilitate the transformation of active P into moderately Ca-bound P. This study proposes a strategy for recycling P-adsorbed materials to mitigate agricultural non-point P pollution.

Mechanisms of Lanthanum-mediated mitigation of salt stress in soybean (Glycine max L.).

Salinity is considered one of the abiotic stresses that have the greatest impact on soybean production worldwide. Lanthanum (La) is a rare earth element that can reduce adverse conditions on plant growth and productivity. However, the regulatory mechanism of La-mediated plant response to salt stress has been poorly studied, particularly in soybeans. Therefore, our study investigated the mechanisms of La-mediated salt stress alleviation from the perspectives of the antioxidant system, subcellular structure, and metabolomics responses. The results indicated that salt stress altered plant morphology and biomass, resulting in an increase in peroxidation, inhibition of photosynthesis, and damage to leaf structure. Exogenous La application effectively promoted the activity of superoxide dismutase (SOD) and peroxidase (POD), as well as the soluble protein content, while decreasing the Na+ content and Na+/K+ ratio in roots and leaves, and reducing oxidative damage. Moreover, transmission electron microscopy (TEM) demonstrated that La prevented the disintegration of chloroplasts. Fourier-transform infrared spectroscopy (FTIR) analysis further confirmed that La addition mitigated the decline in protein, carbohydrates, and pectin levels in the leaves. Lanthanum decreased the leaf flavonoid content and synthesis by inhibiting the content of key substances in the phenylalanine metabolism pathway during NaCl exposure. Collectively, our research indicates that La reduces cell damage by regulating the antioxidant system and secondary metabolite synthesis, which are important mechanisms for the adaptive response of soybean leaves, thereby improving the salt tolerance of soybeans.

Structure-driven development of a biomimetic rare earth artificial metalloprotein.

The 2011 discovery of the first rare earth-dependent enzyme in methylotrophic Methylobacterium extorquens AM1 prompted intensive research toward understanding the unique chemistry at play in these systems. This enzyme, an alcohol dehydrogenase (ADH), features a La3+ ion closely associated with redox-active coenzyme pyrroloquinoline quinone (PQQ) and is structurally homologous to the Ca2+-dependent ADH from the same organism. AM1 also produces a periplasmic PQQ-binding protein, PqqT, which we have now structurally characterized to 1.46-Å resolution by X-ray diffraction. This crystal structure reveals a Lys residue hydrogen-bonded to PQQ at the site analogously occupied by a Lewis acidic cation in ADH. Accordingly, we prepared K142A- and K142D-PqqT variants to assess the relevance of this site toward metal binding. Isothermal titration calorimetry experiments and titrations monitored by UV-Vis absorption and emission spectroscopies support that K142D-PqqT binds tightly (Kd = 0.6 ± 0.2 µM) to La3+ in the presence of bound PQQ and produces spectral signatures consistent with those of ADH enzymes. These spectral signatures are not observed for WT- or K142A-variants or upon addition of Ca2+ to PQQ ⸦ K142D-PqqT. Addition of benzyl alcohol to La3+-bound PQQ ⸦ K142D-PqqT (but not Ca2+-bound PQQ ⸦ K142D-PqqT, or La3+-bound PQQ ⸦ WT-PqqT) produces spectroscopic changes associated with PQQ reduction, and chemical trapping experiments reveal the production of benzaldehyde, supporting ADH activity. By creating a metal binding site that mimics native ADH enzymes, we present a rare earth-dependent artificial metalloenzyme primed for future mechanistic, biocatalytic, and biosensing applications.

Adsorption and recovery of phosphate using sodium carbonate as co-precipitant synthesized La&Zr dual-metal modified material: Adsorption mechanism and practical application.

Adsorption methods offer efficient recovery of phosphorus from water bodies. Modification adsorption materials combining lanthanum (La) and zirconium (Zr) dual-metal immobilized via co-precipitation method have been widely applied in the adsorption and recovery of phosphate. Meanwhile, sodium carbonate (Na2CO3) is gradually replacing sodium hydroxide (NaOH) as the mainstream co-precipitant for immobilizing metals into supporting matrices due to its excellent performance and environmental friendliness. However, the adsorption mechanisms of materials synthesized with different co-precipitants and the synergistic effects between dual-metal components are not well understood, which is not conducive to the further optimization of dual-metal adsorption materials. In this study, anion exchange resin was utilized as the supporting matrices, and La&Zr dual-metal-modified materials, La&Zr-CO32- and La&Zr-OH-, were prepared using Na2CO3 and NaOH as co-precipitants, respectively. The results indicate that La&Zr-CO32- exhibits superior performance in phosphate adsorption and recovery, with adsorption capacity and recovery efficiency reaching 36.28 mg/g and 82.59%, respectively. Additionally, this material demonstrates strong stability in reuse, phosphate selectivity, and a wide pH applicability range. La&Zr-CO32- achieves phosphate adsorption through surface electrostatic affinity, ligand exchange, and intraspherical complexation, whereas La&Zr-OH- primarily relies on electrostatic adsorption on the surface and interior of the material. Synergistic effects between La and Zr result in enhanced adsorption performance of the dual-metal material compared to individual metals. Specifically, phosphate adsorption is predominantly governed by La, while the presence of Zr further enhances ligand exchange between lattice oxygen and metals. Simultaneously, Zr doping enhances the phosphate recovery capacity and reusability of the materials. Continuous flow adsorption results from actual water bodies demonstrate that La&Zr-CO32- is more suitable for the removal and recovery of phosphate in water treatment engineering. This study provides a theoretical basis and technical support for the adsorption and recovery of phosphate using dual-metal-modified materials.

The multistressor effect of pH reduction, microplastic and lanthanum on sea urchin Arbacia lixula.

pH reduction (Low pH), microplastic (MP), and lanthanum (La) are substantial stressors due to their increasing trends in marine ecosystems and having adverse effects on marine species. This study investigates the single and combined effects of those stressors (Low pH: 7.45, polyethylene MP: 26 µg L-1, and La: 9 µg L-1) on the physiology and histology of sea urchin Arbacia lixula. Regarding physiological results, while the coelomocytes' quantity was slightly affected by stressors, their viability was significantly affected. The coelomocyte count and viability were suppressed most in Low pH-MP-La treatment. The stressors did not impact the respiration rate. According to the histological examination results, the crypt (villi-like structure) was shorter, and epithelial layers were thinner in single and dual stress treatments like MP, Low pH, Low pH-La, and MP-La. Overall, we suggest that the combination of variable types of those stressors causes negative effects on sea urchin's physiology and histology.

Lanthanum-doped chitosan-based polyacrylamide double network hydrogels for adsorption of phosphorus from wastewater.

Excessive phosphorus in aqueous solutions can cause eutrophication, which can harm aquatic organisms and pose a risk to the safety of drinking water for humans. The Chitosan/Polyacrylamide/Lanthanum (CS/PAM/La) hydrogel was designed to get rid of phosphate from aqueous solutions. La (III) was used to enhance the capacity of adsorption of CS. Polyacrylamide was used to enhance the mechanical properties of CS. The results showed that the adsorption capacity of CS/PAM/La hydrogel for phosphate was increased compared with that of CS. When pH of 5.0, the adsorption capacity was 80.07 mg-P/g. In addition, after five adsorption and desorption cycles, the adsorption efficiency remained above 90%. The mechanism of phosphate adsorption on CS/PAM/La material was analyzed using a mass transfer factor model (MTF) and the possible structure of CS/PAM/La hydrogel was calculated by density functional theory calculation (DFT). The application of CS/PAM/La composite hydrogel for removal of phosphate from actual wastewater was investigated, and the results met the requirement of national standard.