Search Results (94)

Numerous promising cancer treatments currently in clinical trials rely on the production and purification of actinium-225 (²²⁵Ac), an actinide with alpha emissions that can kill cancer cells via targeted alpha therapy. To enable ongoing and future studies, and to support anticipated future demand, it is necessary to increase the supply of ²²⁵Ac. High-energy proton irradiation of thorium metal (Th⁰_(s)) is one of the leading production methods of ²²⁵Ac. This process requires the chemical separation of microscopic amounts (μg) of ²²⁵Ac from large quantities (>10 g) of thorium. Current methods to accomplish this thorium removal step can be slow, tedious, generate large quantities of radioactive liquid waste, and require very strict control of the processing conditions. To improve this separation, we investigated the ability of four nitrate salts (NH₄NO₃, KNO₃, RbNO₃, and CsNO₃) to act as selective Th⁴⁺ _(aq) precipitation agents in the presence of ²²⁵Ac³⁺_(aq) in aqueous nitric acid to allow for their separation through a simple filtration. First, we used an automated separations platform to screen the ability of these nitrate salts to precipitate Th⁴⁺. We found the Th⁴⁺ precipitation yields and amount of precipitating agent needed to maximize this yield were dependent on the identity of the precipitating agent cation. Separation studies with ²²⁵Ac³⁺_(aq) and subsequent down-selection of the most promising Th⁴⁺ precipitating agents and conditions enabled us to develop its effective selective precipitation. We demonstrated that the separation was compatible with Th⁰_(s) quantities that can produce medically relevant amounts of ²²⁵Ac. We observed 99.9% of Th⁴⁺_(aq) could be removed via precipitation with KNO_3(s) in less than two hours in the presence of co-produced isotopes. Meanwhile, other experiments demonstrated that the ²²⁵Ac³⁺_(aq) recovery was > 97% at 1–10 g Th⁰_(s) scale. Full article

Synthesis of bifunctional cytisine–squaramide derivatives bearing a single amino acid moiety has revealed an unexpected and intriguing chemical challenge. During modification of cytisine squaramates with α-amino acids, base-sensitive amido esters readily underwent hydrolysis, forming poorly soluble amido-acid side products that resisted standard purification and initially obscured their identity. Persistent observation of these elusive precipitates prompted a deliberate co-crystallization approach, which unambiguously revealed their supramolecular nature using single-crystal X-ray diffraction. With this insight, optimized purification strategies allowed isolation of analytically pure Cyt-SQ-OH and its derivatives, which were characterized by complementary spectroscopic techniques, X-ray crystallography and computational studies. Furthermore, the DFT-optimized parameters of all compounds were determined, providing additional insight into their structural and electronic properties. This work highlights the interplay between reactivity, solubility, and supramolecular assembly in cytisine–squaramide-amino acid hybrids, providing a robust platform for future exploration of multifunctional conjugates with potential applications in medicinal chemistry, molecular recognition, and materials science. Full article

The valorization of secondary biomass streams is an important step toward more resource-efficient biorefinery concepts and reduced dependence on fossil-based materials. In this study, agricultural and forest residues, namely Atlas cedar cones, mixed conifer cones, hazelnut shells, walnut shells, coffee silverskin, and cocoa shells, were investigated as feedstocks for producing colloidal lignin particles. Lignin-rich extracts were obtained by Organosolv pretreatment using 60 wt% aqueous ethanol, followed by particle formation through solvent shifting and purification by ultrafiltration. A particular novelty of this work is that highly different feedstocks were processed under identical Organosolv and solvent-shifting conditions, enabling a direct comparison of their suitability for colloidal lignin particle production within one consistent process route. The feedstocks differed markedly in extractive content and chemical profile, as shown by sequential Soxhlet extraction and qualitative GC-MS screening. Despite these differences in extract composition, solvent shifting yielded colloidal lignin particles with largely similar properties. Dynamic light scattering showed hydrodynamic diameters of 65–88 nm immediately after precipitation for all samples except cocoa shell, which formed strong agglomerates. The ultrafiltration step further introduced an industry-relevant downstream purification stage by removing most water-soluble low-molecular-weight compounds before product evaluation. After purification and redispersion, particle sizes ranged from 121 to 389 nm, indicating partial aggregation but overall successful recovery of stable colloidal dispersions. All purified particle suspensions exhibited comparable antioxidant activity in the FRAP (ferric reducing antioxidant power) assay, ranging from 12.3 to 18.4 mg lignin per mg ascorbic acid equivalents. These results demonstrate that even chemically diverse biomass side streams can be converted into purified colloidal lignin suspensions with similar colloidal behavior and functional performance. The findings highlight the potential of low-value agricultural and forest residues as promising raw materials for lignin-based antioxidant and material applications. Full article

This study optimized the extraction, purification, and structural chemical characterization of polysaccharides from fruitless wolfberry bud tea (FWP), and evaluated their antioxidant activities against H₂O₂-induced oxidative damage in SH-SY5Y cells. Crude FWP was obtained by ultrasonic-assisted water extraction followed by ethanol precipitation. An orthogonal experiment was conducted to optimize decolorization using D301G macroporous resin, achieving a decolorization rate of 74%, a polysaccharide retention rate of 85%, and a protein removal rate of 61%. Two main purified polysaccharide fractions, FWP-1 (52.3 kDa) and FWP-2 (9.95 kDa), were isolated by DEAE-52 and Sephadex G-150 chromatography. Structural analysis revealed that FWP-1 was a neutral heteropolysaccharide rich in glucose and galactose, while FWP-2 was an acidic polysaccharide with a high content of galacturonic acid. In H₂O₂-induced SH-SY5Y cells, both polysaccharides significantly enhanced cell viability, increased superoxide dismutase (SOD), catalase (CAT), and glutathione (GSH) levels, reduced lactate dehydrogenase (LDH) leakage and malondialdehyde (MDA) content, scavenged excessive reactive oxygen species (ROS), and maintained mitochondrial membrane potential. FWP-2 exhibited stronger ROS-scavenging capacity than FWP-1. This study established reliable methods for the purification and characterization of FWP, and verified their potential as natural antioxidants against neuronal oxidative injury. Full article

This study addresses the issue of insufficient product purity caused by the co-deposition of three major impurity ions—zinc, nickel, and lead—during the electrodeposition process of high-purity manganese. A targeted deep purification method for manganese sulfate electrolyte was developed using dithiocarbamate chelating agents (sodium dimethyldithiocarbamate, SDD). By optimizing key process parameters such as precipitant concentration, reaction temperature, reaction time, and solution pH, combined with density functional theory (DFT) calculations, to elucidate the selective impurity removal mechanism at the molecular level, a novel process for the efficient synergistic removal of Zn²⁺, Ni²⁺, and Pb²⁺ was established. The results showed that under the conditions of precipitant concentration of 1 g/L, solution pH of 6.5, reaction temperature of 55 °C, and reaction time of 2 h, the residual concentrations of Zn, Ni, and Pb in the electrolyte were all below 0.2 mg/L. DFT calculations revealed that SDD coordinates with metal ions through four sulfur atoms, and the absolute values of binding energies follow the order Ni²⁺ > Pb²⁺ > Zn²⁺ > Mn²⁺, indicating thermodynamically preferential capture of impurity ions. After purification, the manganese metal obtained by electrodeposition from the manganese sulfate solution achieved a purity exceeding 99.999%, with Zn, Ni, and Pb contents of 0.11 mg/kg, 0.038 mg/kg, and 0.05 mg/kg, respectively, meeting the raw material requirements for semiconductor-grade copper–manganese alloy targets. Full article

To prevent fouling in blast furnace gas top pressure recovery turbine units, the dust content of the gas must be reduced, necessitating its deep purification. A critical challenge to be addressed is the low collection efficiency of fine particulate matter. To improve the collection efficiency of the fine particulate dust in BFG by wet electrostatic precipitators (WESPs), this study implemented measures such as optimizing nozzle atomization performance and the spatial distribution of droplets, along with adding chemical agglomeration agents and surfactants. These approaches promoted the chemical agglomeration of fine dust and enhanced dust collection efficiency. In this study, five nozzle types, six chemical agglomerating agents, and three surfactants were tested. The results show that, under overlapping spray conditions, the 1/8 solid cone nozzle produced the smallest droplet size with the most uniform spatial distribution, exhibiting a d50 of 141.17 μm. When this nozzle was used in combination with guar gum (GG) as a chemical agglomerant, the d50 of BFG dust increased from 8.46 μm to 14.75 μm. The synergistic application of 5 mg/m³ sesbania gum (SBG) and 5 mg/m³ octylphenol ethoxylate (OP-10) further increased the dust d50 to 19.08 μm. Using the 1/8 solid cone nozzle and an XTG concentration of 5 mg/m³ resulted in the highest dust collection efficiency of 96.76%, while the synergistic use of SBG/OP-10 achieved an efficiency of 97.69%. This study elucidates the influence of nozzle atomization characteristics and spray liquid type on dust agglomeration and collection efficiency, achieving an improvement in dust-removal efficiency and the capture of fine-particulate dust, and providing both theoretical and practical foundations for the deep purification of blast furnace gas. Full article

Conventional bioretention systems face challenges in effectively removing dissolved nutrients, heavy metals, and emerging contaminants from stormwater runoff. This study investigates the application of thermally modified steel slag (700 °C) as a functional bioretention matrix for comprehensive stormwater purification. Three pilot-scale systems were evaluated over 120 days: Control (biochar-zeolite), Unmodified (raw steel slag-biochar-zeolite), and Modified (thermally modified steel slag-biochar-zeolite). The modified system demonstrated superior and stable removal efficiencies for NH₄⁺-N (95.3 ± 1.3%), TN (85.7 ± 1.8%), TP (90.5 ± 1.5%), Cu²⁺ (96.1 ± 0.7%), Cr⁶⁺ (90.5 ± 1.2%), Pb²⁺ (92.2 ± 1.1%), enrofloxacin (65.6 ± 2.1%), and norfloxacin (62.6 ± 2.4%). Performance remained robust under varying hydraulic conditions, with high removal maintained across rainfall return periods (0.5–2 years) and antecedent dry periods (2–8 days). Mechanistic investigations revealed synergistic effects: (1) Enhanced physical adsorption through increased surface area (2.338 m²/g) and pore volume (0.109 cm³/g); (2) Chemical precipitation via Ca²⁺/Fe³⁺ release at alkaline pH (8.2–8.5); (3) Enriched microbial communities with 35% higher Shannon diversity, particularly Hydrogenophaga (12.3%) for autotrophic denitrification using Fe²⁺ as electron donor. The modified slag matrix creates a “triple-barrier” removal mechanism combining physical, chemical, and biological processes, offering an efficient solution for multi-pollutant stormwater treatment. This study demonstrates that thermally modified steel slag represents a high-performance, cost-effective bioretention matrix for comprehensive stormwater treatment while promoting industrial byproduct utilization and aligning with circular economy principles. Full article

The conventional production of electronic-grade, high-purity, spherical silicon dioxide (SiO₂) faces challenges of high raw material costs and poor control over particle morphology. This study presents an alternative route using low-cost, powdered quartz as a starting material. The quartz was first purified by flotation to remove any associated minerals, such as talc. Subsequently, deep purification was achieved through a hydrothermal alkaline process, which leveraged the distinct leaching kinetics of SiO₂ and impurity ions (Al³⁺, Ca²⁺, Fe³⁺) under precisely controlled hydrothermal conditions (10 mL/g liquid-to-solid ratio, 3 mol/L NaOH, 200 °C, 8 h). This step yielded a sodium silicate solution with a purity of 99.999%. Spherical SiO₂ particles were then synthesized from solutions of varying moduli via chemical precipitation. The condensation kinetics of silicate anionic species (Qn) during acidification were investigated, revealing how the Qn distribution governs the final particle size and morphology. The optimal product exhibited excellent characteristics: a sphericity ≥ 0.98, a median particle size (D₅₀) of 400–500 nm, and a narrow particle size distribution (polydispersity index, PDI of 0.178–0.192). These properties surpass the requirements for the QYG-H Type 002 grade specified in the Chinese National Standard GB/T 32661-2016 (“Spherical Silica Powder”) and meet the standard for electronic-grade spherical SiO₂. This work provides a fundamental insight into morphology control and a feasible technical pathway for the value-added utilization of powdered quartz and the production of electronic-grade spherical SiO₂ with a narrow particle size distribution. Full article

Soybean, as a globally important economic crop, is severely threatened by Sclerotinia sclerotiorum, the causative agent of Sclerotinia stem rot (SSR), a major disease in soybean production worldwide, leading to significant yield losses and quality deterioration. Traditional chemical control methods face challenges such as environmental pollution, pesticide resistance, and limited efficacy. Bacillus velezensis YJ0-1, identified through plate confrontation assays, demonstrated significant inhibitory effects on S. sclerotiorum via acid-precipitated crude extracts from its fermentation broth. A key antimicrobial substance, fengycin (C₇₂H₁₁₀N₁₂O₂₀, molecular weight 1463.8 Da), was isolated and characterized through acid precipitation, protein purification system separation, and mass spectrometry (MS). Further optimization of the PDB medium using single-factor experiments and Box–Behnken design yielded an optimal formulation: peptone 66.62 g/L, sucrose 32.68 g/L, and pH 6.5. Validation experiments showed an actual yield of 2.03 g/L, with a relative error of only 0.49% compared to the predicted yield of 2.04 g/L, significantly enhancing the synthesis efficiency of fengycin. This study provides novel microbial resources and a theoretical basis for the biological control of SSR in soybeans, while also laying a technical foundation for the industrial production of fengycin, contributing to the advancement of sustainable agriculture. Full article

Background/Objectives: Calsequestrin (CSQ) is a calcium-binding protein that is highly soluble and can serve as a solubility-enhancing fusion tag in recombinant protein expression. Its unique property of calcium-induced precipitation followed by EDTA-mediated resolubilization enables efficient purification. However, the broader application of CSQ-tagged proteins in research have been hampered by the lack of reliable anti-CSQ detection reagents. This study aimed to develop single-domain antibodies (sdAbs) against CSQ for use in diverse immunoassays and cell-based analyses. Methods: Single-domain antibodies were selected from phage-displayed chicken VH libraries generated from CSQ-immunized chickens. After biopanning, CSQ-specific VH sdAb clones were isolated and expressed as VH–human kappa light chain constant region (VH-Cκ) fusion proteins in E. coli. The PE06 clone was chosen for further characterization and conjugated to horseradish peroxidase (HRP) and Alexa Fluor 647 for assay applications. Results: PE06 VH-Cκ fusion protein demonstrated specific binding to CSQ-tagged proteins and enabled reliable detection in enzyme-linked immunosorbent assay (ELISA), immunoblotting, and flow cytometry. These results validated its utility as a chemically defined detection reagent for CSQ fusion proteins expressed in E. coli. Conclusions: This study establishes a CSQ-specific chicken VH sdAb as a versatile detection tool for CSQ-tagged proteins. The approach expands the utility of CSQ as a protein fusion tag and enables the development of recombinant antibodies fused with CSQ, such as scFv-CSQ constructs, for broad application in research and assay systems. Full article

The excessive emission of cadmium (Cd²⁺) poses a serious threat to the aquatic environment due to its high toxicity and bioaccumulation potential. This study constructed three types of vertical-subsurface-flow constructed wetlands configured with iron–carbon–zeolite composite substrates, including an iron–carbon–zeolite constructed wetland (TF-CW), a zeolite–iron–carbon constructed wetland (FT-CW), and an iron–carbon–zeolite mixed constructed wetland (H-CW), to investigate the purification performance and mechanisms of constructed wetlands for cadmium-containing wastewater (0~6 mg/L). The results demonstrated that iron–carbon–zeolite composite substrates significantly enhanced Cd²⁺ removal efficiency (>99%) through synergistic redox-adsorption mechanisms, where the iron–carbon substrate layer dominated Fe-Cd co-precipitation, while the zeolite layer achieved short-term cadmium retention through ion-exchange adsorption. FT-CW exhibited superior NH₄⁺-N removal efficiency (77.66%~92.23%) compared with TF-CW (71.45%~88.05%), while iron–carbon micro-electrolysis effectively inhibited NO₃⁻-N accumulation (<0.1 mg/L). Under cadmium stress, Typha primarily accumulated cadmium through its root systems (>85%) and alleviated oxidative damage by dynamically regulating antioxidative enzyme activity, with the superoxide dismutase (SOD) peak occurring at 3 mg/L Cd²⁺ treatment. Microbial community analysis revealed that iron–carbon substrates promoted the relative abundance of Bacteroidota and Patescibacteria as well as the enrichment of Saccharimonadales, Thauera, and Rhodocyclaceae (genera), enhancing system stability. This study confirms that iron–carbon–zeolite CWs provide an efficient and sustainable technological pathway for heavy metal-contaminated water remediation through multidimensional mechanisms of “chemical immobilization–plant enrichment–microbial metabolism”. Full article

Electrolytic manganese residue (EMR) is a byproduct of electrolytic manganese production, rich in soluble pollutants such as manganese and ammonia nitrogen. Traditional stockpiling methods result in contaminant leaching and water pollution, threatening ecosystems. Meanwhile, EMR has significant resource-recovery potential. This paper systematically reviews the harmless process and resource technology of EMR, efficiency bottlenecks, and the current status of industrial applications. The mechanisms of chemical leaching, precipitation, solidification, roasting, electrochemistry, and microorganisms were analyzed. Among these, electrochemical purification stands out for its efficiency and environmental benefits, positioning it as a promising option for broad industrial use. The mechanisms of chemical leaching, precipitation, solidification, roasting, electrochemistry, and microorganisms were analyzed, revealing the complementarity between building materials and chemical materials (microcrystalline glass) in scale and high-value-added production. But the lack of impurity separation accuracy and market standards restricts its promotion. Finally, it proposes future directions for EMR resource utilization based on practical and economic considerations. Full article

Brine purification is an important process unit in chlor-alkali industrial plants for the production of sodium hydroxide, chlorine, and hydrogen. The membrane cell process requires ultrapure brine, which is obtained through mechanical filtration, chemical precipitation and fine polishing, and ion exchange using polymer resins. Temperature variations can lead to the degradation of the exchange properties of these resins, primarily causing a decrease in their exchange capacity, which negatively impacts the efficiency of the brine purification. After multiple ion exchange regeneration cycles, significant quantities of spent resins may be generated. These must be managed in accordance with resource efficiency and hazardous waste management to ensure the sustainability of the industrial process. In this paper, a comparative study is conducted to characterize the long-term stability of a new commercial chelating resin used in the industrial electrolysis process. The spectroscopic methods of physicochemical characterization included: scanning electron microscopy with energy dispersive X-ray spectroscopy (SEM-EDX) and attenuated total reflectance–Fourier transform infrared spectroscopy (ATR-FTIR). The thermal behavior of the polymer resins was evaluated using the following thermogravimetric methods: thermogravimetry (TG), derivative thermogravimetry (DTG), and differential thermal analysis (DTA), while the moisture behavior was studied using dynamic vapor sorption (DVS) analysis. To assess the energy potential, the polymer resins were analyzed to determine their calorific value and overall energy content. Full article

Rhenium metal is extensively utilized in the aerospace industry for the manufacturing of various superalloys due to its unique properties, and plays an indispensable role in the field of high technology. Rhenium resources are primarily associated with copper, molybdenum, and other metal ores. Ammonium perrhenate is predominantly derived from copper and molybdenum ore roasting flue gas scrubbers containing various impurities in the rhenium-containing contaminated acid. The complex composition of the contaminated acid renders the enrichment and purification of ammonium perrhenate more challenging, necessitating further research and development of the technology. This paper reviews the research progress in ammonium perrhenate enrichment and purification technology, encompassing chemical precipitation, adsorption, extraction, ion exchange, extraction chromatography, and recrystallization. It analyses the advantages and limitations of various methods, with the aim of providing a reference for future developments in ammonium perrhenate enrichment and purification technology. Furthermore, the paper presents a prospective view on the development of ammonium perrhenate enrichment and purification technology, focusing on the objective of obtaining more selective purification materials and more efficient purification techniques for ammonium perrhenate. Full article

Recycling of spent lithium-ion batteries is important due to the increasing demand for electric vehicles and efforts to realize a circular economy. There is a need to develop environmentally friendly processes for the refining of nickel, cobalt, and other metals contained in the batteries. Electrodialysis is an appealing method for recycling of battery metals with selective separation and low chemical input. In this study, sodium sulfate was used in an electrodialysis metathesis procedure to sequentially separate EDTA-chelated nickel and cobalt. Replacing hitherto used sulfuric acid with sodium sulfate mitigates membrane fouling caused by precipitation of EDTA. It was possible to separate up to 97.9% of nickel and 96.6% of cobalt at 0.10 M, a 30-times higher concentration than previously reported for electrodialysis of similar solutions. Through the thermally activated persulfate method, new to this application, 99.7% of nickel and 87.0% of cobalt could be precipitated from their EDTA chelates. Impurity behavior during electrodialysis of battery leachates has not previously been described in the literature. It is paramount to remove copper, iron, and phosphorous prior to electrodialysis since they contaminate the nickel product. Aluminum was difficult to remove in the solution purification step and ended up in all electrodialysis products. Full article