Bulk Solution Research Articles

Lyso-phosphatidylcholine as an interfacial stabilizer for parenteral monoclonal antibody formulations

Therapeutic proteins suffer from physical and chemical instability in aqueous solution. Polysorbates and poloxamers are often added for protection against interfacial stress to prevent protein aggregation and particle formation. Previous studies have revealed that the hydrolysis and oxidation of polysorbates in parenteral formulations can lead to the formation of free fatty acid particles, insufficient long-term stabilization, and protein oxidation. Poloxamers, on the other hand, are considered to be less effective against protein aggregation. Here we investigated two lyso-phosphatidylcholines (LPCs) as potential alternative surfactants for protein formulations, focusing on their physicochemical behavior and their ability to protect against the formation of monoclonal antibody particles during mechanical stress.The hemolytic activity of LPC was tested in varying ratios of plasma and buffer mixtures. LPC effectively stabilized mAb formulations when shaken at concentrations several orders of magnitude below the onset of hemolysis, indicating that the potential for erythrocyte damage by LPC is non-critical. LPC formulations subjected to mechanical stress through peristaltic pumping exhibited comparable protein particle formation to those containing polysorbate 80 or poloxamer 188. Profile analysis tensiometry and dilatational rheology indicated that the stabilizing effect likely arises from the formation of a viscoelastic film at approximately the CMC. Data gathered from concentration-gradient multi-angle light scattering and isothermal titration calorimetry support this finding. Surfactant desorption was evaluated through sub-phase exchange experiments. While LPCs readily desorbed from the interface, resorption occurred rapidly enough in the bulk solution to prevent protein adsorption. Overall, LPCs behave similarly to polysorbate with respect to interfacial stabilization and show promise as a potential substitute for polysorbate in parenteral protein formulations.

Self-Assembled Triangular Prismatic Cages with Kinetic Inertness.

Two triangular prismatic cages were synthesized by combining a trishydrazide and two bisformyl precursors in strongly acidic water, where the dynamic nature of hydrazone was turned ON. An anionic guest was used as the template to drive the cage formation. Performing counterion exchange removed both the template and the Brønsted acid. The removal of the latter afforded the cages' kinetic inertness by turning OFF the reversibility of hydrazone. The cages can thus be used for recognizing various guests in water without observable degradation, driven by the hydrophobic effect. Upon being accommodated within the cage cavities, an anthracene derivative was protected from UV-stimulated oxidation, which would occur otherwise in the bulk solution without the protection from the host.

Impact of surface hydrophilicity on the ordering and transport properties of bicontinuous microemulsions.

Microemulsions (MEs) have many industrial applications, where recent developments have shown that MEs can be utilized for electrochemical applications, including potentially in redox flow batteries. However, understanding the structure and dynamics of these systems, including at a surface, is needed to direct and rationally control their electrochemical behavior. While bulk solution measurements have provided insight into their structure, their assembly at an interface also impacts the electron (to the electrode) and ion (across the surfactant) charge transfer processes in the system. To address this shortcoming, neutron reflectivity experiments and molecular simulations have been completed that document the near surface structure of a series of deuterated water (D2O)/polysorbate-20/toluene MEs on hydrophilic and amphiphilic surfaces. These results show that the microemulsions form complex layered structures near a hard electrode surface, where most layers are not purely one component. Decreasing the D2O concentration in the ME increases the number of and purity of the layers established on the solid surface. These lamellar-type layers transition from the surface to the bulk microemulsion as a series of mixed layers (i.e., containing oil, water, and surfactant) that are consistent with perforated lamellae. Additionally, these mixed lamellae appear to become more perforated with oil and water pathways on an amphiphilic surface. The purity and thickness of these layers will influence the accessibility of an electrode by redox active species, as well as ion transport required to satisfy the electroneutrality condition.

Covalent Au-C Contact Formation and C-C Homocoupling Reaction from Organotin Compounds in Single-Molecule Junctions.

Formation of new chemical species has been achieved under an electric field by the use of the scanning tunneling microscope break junction technique, yet simultaneous implementation of catalytic reactions both at the organic/metal interface and in the bulk solution remains a challenging task. Herein, we show that n-butyl-substituted organotin-terminated benzene undergoes both an efficient cleavage of the terminal tributyltin group to form a covalent Au-C bond and a homocoupling reaction to yield biphenyl product when subjected to an electric field in the vicinity to Au electrodes. By using ex situ characterization of high-performance liquid chromatography with an UV-vis detector, we demonstrate that the homocoupling reaction can occur with high efficiency under an extremely low tip bias voltage of ∼5 mV. Additionally, we show that the efficiency of the homocoupling reaction varies significantly in different solvents; the choice of the solvent proves to be one of the methods for modulating this reaction. By synthesizing and testing varied molecular backbone structures, we show that an extended biphenyl backbone undergoes homocoupling to form a quarterphenylene backbone, and the C-C coupling reactions are prohibited when additional aurophilic or bulky chemical groups that exhibit a steric blockage are introduced.

Numerical modeling of electromagnetic field spatiotemporal evolution to evaluate the effects on calcium carbonate crystallization

Calcium carbonate (CaCO3) scaling is a significant impediment to water systems. Electromagnetic field (EMF) treatment is a promising approach to control scaling owing to its simplicity and low or no energy requirements. However, the underlying mechanisms by which EMF impacts CaCO3 crystallization remain unclear due to the challenges in measuring the EMFs in feed solutions and the lack of a fundamental understanding of the applied EMFs and the observed physicochemical phenomena. To fill this knowledge gap, a high-fidelity COMSOL model was first developed to simulate EMFs in bulk solutions for three alternating current-induced EMF devices with different configurations and properties. These were then integrated with experimental data to unveil the underlying mechanism by which applied EMFs alter the physicochemical processes. The study revealed that even low-strength EMFs (e.g., electric fields <0.15 V/m and magnetic fields <0.03 mT) promoted CaCO3 precipitation in bulk solutions. The electric fields created by these EMF devices resulted in higher Lorentz force compared to their induced magnetic fields. The methodology of this study offers the capability to predict the effectiveness of different EMF devices in facilitating crystallization processes, and these mechanistic insights lay the foundation for the smart design of EMF devices for diverse water treatment applications.

Biosensor Based on ZIF-67-HRP and MWCNTs Nanocomposite Modified Glass Carbon Electrode for the Detection of Luteolin in Vegetables.

Luteolin has various pharmacological properties, including anti-inflammatory, antioxidant, and antitumor characteristics. Due to its potential value in drugs and functional foods, it is important to develop an efficient method for detecting luteolin. In this work, the poor selectivity of existing luteolin nonenzymatic sensors was solved by translating the enzyme-catalyzed reaction from bulk solution to the surface of a horseradish peroxidase (HRP) modified electrode through an electrocatalytic oxidation process. Here, we modified the surface of a glassy carbon electrode (GCE) with metal-organic frameworks (MOFs; ZIF-67 here, abbreviated as ZIF), functional nanomaterials, and HRP and finally covered it with Nafion (NF). In this case, luteolin acts as a hydrogen donor, and the electrode acts as a hydrogen acceptor; the oxidation reaction occurs on the electrode surface. The use of ZIF-67 ensured the conformational stability of HRP to ensure the selectivity and anti-interference property, and SDS-dispersed multiwalled carbon nanotubes (MWCNTs) enhanced the electrode conductivity. The use of NF avoids shedding of the electrode material during the testing process. A UV-vis spectrophotometer was used to study the selectivity of luteolin by HRP and the compatibility between HRP and ZIF. The materials were characterized and analyzed by scanning electron microscopy and transmission electron microscopy. Due to the synergistic effect of these nanomaterials, the linear range of NF/ZIF-HRP/MWCNTs-SDS/GCE was 1.0 × 10-2 to 6.0 μM, with detection limits of 25.3 nM (S/N = 3). The biosensor showed long-term stability and reproducibility, with a relative standard deviation of 4.2% for the peak current (n = 5). Finally, the biosensor was successfully used to detect luteolin in carrots, celery, and cauliflower.

PH Affects the Spontaneous Formation of H2O2 at the Air-Water Interfaces.

Recent studies have shown that the air-water interface of aqueous microdroplets is a source of OH radicals and hydrogen peroxide in the atmosphere. Several parameters such as droplet size, salt, and organic content have been suggested to play key roles in the formation of these oxidants. In this study, we focus on the effect of acidity on the spontaneous interfacial hydrogen peroxide formation of salt-containing droplets. Na2SO4, NaCl, and NaBr bulk solutions, at the range of pH 4 to 9.5, were nebulized, using ultra high-purity N2/O2 (80%/20%), and H2O2 was measured in the collected droplets. All of the experiments were performed in T = 292 ± 1 K and humidity levels of 90 ± 2%. For Na2SO4 and NaCl, the H2O2 concentration was increased by ∼40% under alkaline conditions, suggesting that OH- enriched environments promote its production. When CO2 was added in the ultrapure air, H2O2 was observed to be lower at higher pH. This suggests that dissolved CO2 can initiate reactions with OH radicals and electrons, impacting the interfacial H2O2 production. H2O2 formation in NaBr droplets did not display any dependence on the pH or the bath gas, showing that secondary reactions occur at the interface in the presence of Br-, which acts as an efficient interfacial source of electrons.

Utilizing a hydrophobic primary container surface to reduce the formation of subvisible particles in monoclonal antibody solution caused by fluid shear

The exposure of protein molecules to interfaces may cause protein aggregation and particle formation in protein formulations, especially hydrophobic interfaces, which may promote protein aggregation in solution. In this study, we found that modification of the surface properties by application of a hydrophobic Octadecyltrichlorosilane (OTS) could reduce the generation of protein aggregates and particles in protein solution induced by fluid shear. A stable protein adsorption layer was formed at the hydrophobic interface through the strong hydrophobic interaction between the protein and hydrophobic surface, which could prevent the aggregated protein from falling off into the bulk solution to form subvisible particles and insoluble protein aggregates. In addition, human complement enzyme linked immunosorbent assay results showed that the particles that were generated in the OTS-coated container did not activate human complement which indicated the OTS-coated container could be used as primary containers for certain types of monoclonal antibody formulation.

X-ray Induced Cycling of Rare-Earth Elements between Bulk and Interfacial Liquid.

Reversible cycling of rare-earth elements between an aqueous electrolyte solution and its free surface is achieved by X-ray exposure. This exposure alters the competitive equilibrium between lanthanide ions bound to a chelating ligand, diethylenetriamine pentaacetic acid (DTPA), in the bulk solution and to insoluble monolayers of extractant di-hexadecyl phosphoric acid (DHDP) at its surface. Evidence for the exposure-induced temporal variations in the lanthanide surface density is provided by X-ray fluorescence near total reflection measurements. Comparison of results when X-rays are confined to the aqueous surface region to results when X-rays transmit into the bulk solution suggests the importance of aqueous radiolysis in the adsorption cycle. Amine binding sites in DTPA are identified as a likely target of radiolysis products. The molecules DTPA and DHDP are like those used in the separation of lanthanides from ores and in the reprocessing of nuclear fuel. These results suggest that an external source of X-rays can be used to drive rare-earth element separations. More generally, use of X-rays to controllably dose a liquid interface with lanthanides could trigger a range of interfacial processes, including enhanced metal ion extraction, catalysis, and materials synthesis.

Magnetic Micromotors with Spiky Gold Nanoshells as SERS Sensors for Thiram and Bacteria Detection.

Surface-enhanced Raman scattering (SERS) is widely used in all kinds of detection due to its ultrahigh sensitivity and selectivity. Micromotors, when used as SERS sensors, or the so-called "hotspots on the fly", can combine both controlled mobility and SERS sensing capacity, and are ideal for versatile in situ detection. In this work, mobile SERS sensors are successfully fabricated by growing gold nanospikes onto magnetic microsphere surfaces. These mobile micromotors can act as normal SERS sensors, characterized by the trace detection of thiram, a highly toxic fungicide. The detection limit can reach 0.1nM, as good as most other noble metal deposited substrates. With significant magnetic gradient forces, separation of pathogenic bacteria from bulk solution is achieved once these magnetic micromotors bind with bacterial cells. Manipulated propulsion of micromotors, on the other hand, enables them to approach and contact pathogenic bacterial cells on command and further acquire Raman spectra under a controlled degree of contact, a capability never seen with passive sensors. The robotic SERS sensors have demonstrated unique sensing characteristics with controlled manipulations along with discriminative detection between bacterial species.

Scaling behavior of cation exchange membrane induced by Ca2+ during the electrodialysis for enriching lithium-containing solutions

Membrane fouling, particularly Ca2+-induced scaling on cation exchange membranes (CEM), hinders the application of electrodialysis in lithium extraction. This study investigated the fouling mechanisms of Ca2+ coexisting with Cl− and SO42− on sulfonated CEM, using CaCl2 and CaSO4 solution as the targeted foulants. The conductivity, pH, turbidity, particle size distribution, chemical composition and morphology of the membrane surface were monitored to verify the evolution of the bulk solution and the membrane during the Ca2+-induced fouling. Online detection of conductivity and pH revealed distinct trends in fouling solutions containing Ca2+-Cl- and Ca2+-SO42-. Noticeable changes in turbidity and particle distribution were observed in the concentrated chamber of the highly saturated Ca2+-SO42- solution, whereas the concentrated chamber of the Ca2+-Cl- solution showed turbidity and particle size distribution similar to the initial values. SEM showed that there are different morphologies of scaling crystals in the two types of solution. These fundamental differences are the root cause of the distinct fouling mechanisms between the Ca2+-Cl- solution and Ca2+-SO42- solution. To further investigate the fouling mechanisms, the electrochemical impedance spectroscopy (EIS) was employed to differentiate the impedance of the electric double layer and diffusion layer, providing insights into the characteristics of the CEM-solution interfaces fouled by different lithium-containing solutions. Additionally, adsorption experiments, quartz crystal microbalance with dissipation (QCM-D) and computational simulations (COMSOL, DFT) were conducted to provide detailed insights into the effects of fouling solutions on the properties of the desalted solution, the probability of crystal precipitation, and particularly the interaction between Ca2+ and the functional sites on the CEM. Finally, the Ca2+-induced scaling mechanism of CEM for enriching the lithium-containing solutions with and without SO42− was proposed, elucidating the synergistic effects of Ca2+-induced crystallization in the bulk solution and Ca2+ adsorption on the CEM surface. The research results could offer theoretical guidance for developing pollution control strategies.

Design of Dendritic Foldamers as Catalysts for Organic Synthesis

Background:: Multistranded foldamers mimic biopolymer architecture, through the assembly and folding of intrinsically flexible polymeric chains attached to polyol core have been synthesised here. The synthesised dendritic motifs possess helical cavities with properly arranged active sites. As these cavities are large enough to accommodate guest molecules, their application as synthetic foldamer catalyst were investigated in Knoevenagel and Mannich reactions. Methods:: It is presumed to be the potentiality of dendritic foldamers to form reverse micelle in the interior of helical motif containing many reactive sites. Results:: Inside the dendritic foldamer, the substrates are adequately concentrated, work together in cooperation for ligand-binding, and stabilize the transition state as in enzymes that helps to accelerate the reaction rate many times greater than in bulk solution. Conclusion:: An unrivalled reaction rate and high yield of products were obtained within a short time in both Knoevenagel and Mannich reactions by using dendritic foldamers as catalysts.

Rare earth europium recovery using selective metal-organic framework incorporated mixed-matrix membrane

Rare-earth elements (REEs) play a crucial role in state-of-the-art technologies and sustainable energy generation. However, conventional production methods of REE often instigate detrimental impacts on environment. Hence, the development of efficient and sustainable hydrometallurgical methods for REE recovery from complex solution has become a crucial research focus. This study investigates a mixed-matrix membrane composed of a highly europium selective metal-organic framework-based adsorbent, Cr-MIL-PMIDA, embedded in sulfonated poly(ether ketone) (SPEK) polymer membrane matrix to preferentially concentrate europium (Eu3+) ions in the presence of other competing cations. The activated membrane notably reduced ionic conductivity for Eu3+ compared to other multivalent ions. Membrane extraction experiments further confirmed the selective behavior, demonstrating slower diffusion for Eu3+ compared to Mg2+ and Zn2+ cations. Especially, at pH 5, Mg2⁺ and Zn2⁺ recovery was greater than 30%, whereas Eu³⁺ recovery remained lower than 4%. We propose that the strong chemical affinity between the phosphate group and Eu3+ help partition of the Eu3+ ions in the membrane phase and inhibit the diffusion and further partitioning of the Eu3+ ion from bulk solution. Furthermore, we demonstrate the stability of the composite membrane and the embedded MOF particles in aqueous solution for up to 12 days without degradation, attributing it to the robust chemical stability of the MOF structure.

Electrochemical treatment on a pilot scale of a mixture with high concentrations of dyes from the tanning/textile industry

Violet LR (VLR), Brown RD (BRD), and Green A (GA) dyes are widely used in the tannery industry for dyeing leather. These types of compounds can be toxic and, in many cases, carcinogenic. In this context, electrochemical oxidation (EO) and electro-Fenton (EF) processes are the most popular electrochemical advanced oxidation processes (EAOPs) to degrade persistent/toxic water pollutants. The efficiency of these processes largely depends on the nature of the electrode materials, among other operation parameters. This study evaluates Ti/IrO2-SnO2-Sb2O and BDD anodes for dye degradation in a pilot plant of 4.0 L of total volume. It was found that DSA IrO2-SnO2-Sb2O performed better than BDD for the discoloration of a mixture of the dyes (kDSA=0.0970 min−1 and kBDD=0.0370 min−1) in a medium containing 50 mM NaCl and 10 mM Na2SO4 (j = 50 mA cm−2, Q=12 L min−1 and pH 3). Such an effect was due to the combined production of heterogeneous •OH at the anode surface by H2O oxidation and reactive chlorinated species in the bulk solution via Cl- oxidation. In addition, •OH quantification showed a higher production by DSA ([BDD(•OH)] = 3,8 × 10-15 M vs [DSA(•OH)] = 6.6 × 10-15 M). The efficiency was enhanced when applying EF (BDD cathode promoting H2O2 production) in the presence of Fe2+ ions under similar experimental conditions. The color was almost totally removed in 50 min with kEF-DSA=0.1584 min−1, while COD was removed by 80 % in 80 min. The EC was 0.082 kWh (g COD)-1. Such results highlight the potential of EO and EF with accessible Ti/IrO2-SnO2-Sb2O anodes as a pretreatment unit within a treatment train for tanning or textile wastewater management.

De Novo Design and Characterization of Amphiphilic Peptides with Basic Side Chains for Tailored Interfacial Chemistries.

Lysine-leucine (LK) peptides have been used as model systems and platforms for 2D material design for decades. LK peptides are amphiphilic sequences designed to bind and fold at hydrophobic surfaces through hydrophobic leucine side chains and hydrophilic lysine side chains extending into the aqueous subphase. The hydrophobic periodicity of the sequence dictates the secondary structure at the interface. This robust design makes them ideal candidates for controlling interfacial chemistry. This study presents the de novo design and characterization of two novel peptides: LRα14 and LHα14, which substitute lysine with arginine and histidine, respectively, in the helical LKα14 sequence. This modification is intended to expand the LK peptide platform to a new basic interfacial chemistry. We explore the stability of the new LRα14 and LHα14 designs with respect to changes in pH and salt concentration in bulk solution and at the interface using circular dichroism (UV-CD) and vibrational sum-frequency generation spectroscopy, respectively. Notably, the structural stability of the peptides remains unaffected across a wide range of pH and ionic strength values. At the same time, the variation of side-chain chemistry leads to a wide spectrum of interfacial water structures. By extension of the LK platform to include arginine and histidine, this study broadens the toolbox for designing tailored interfacial chemistries with applications in material and biomedical sciences.

Development of a Stable Lyophilized Cyclophosphamide Monohydrate Formulation Using Non-Aqueous Solvents.

To ensure product stability, it is critical to maintain the monohydrate state of cyclophosphamide following lyophilization, as this is the most stable solid form of the Cyclophosphamide. On the other hand, because of their limited aqueous solubility and stability, non-aqueous solvents are preferred for determining the composition and stability of bulk solutions. Hence, the purpose of this study was to use non-aqueous solvents for determining the composition and stability of bulk solutions, and to shorten the lyophilization process by retaining the cyclophosphamide monohydrate. Furthermore, prior to selecting the solvent for the bulk solution consisting of 90:10 tertiary butyl alcohol (TBA) and acetonitrile (ACN), various factors were taken into account, including the freezing point, vapor pressure of solvents, solubility, and stability of cyclophosphamide monohydrate. The concentration of the bulk solution was adjusted to 200mg/mL in order to optimize the fill volume, enhance sublimation rates at lower temperatures during primary drying, and eliminate the need for secondary drying. The differential scanning calorimetry (DSC) measurements of bulk solution were used to improve the lyophilization cycle. The lyophilization cycle opted was freezing at a temperature of -55°C with annealing step at -22°C by which the reconstitution time was significantly reduced. The drying was performed at below - 25°C while maintaining a chamber pressure of 300 mTorr. The complete removal of non-aqueous solvents was achieved by retaining water within the system. The presence of cyclophosphamide monohydrate was confirmed using X-ray diffraction (XRD). The reduction of lyophilization process time was established by conducting mass transfer tests and evaluating the physicochemical properties of the pharmaceutical product. Using non-aqueous solvents for freeze-drying cyclophosphamide is a viable option, and this study provides significant knowledge for the advancement of future generic pharmaceuticals.

The Electrochemical Peroxydisulfate-Oxalate Autocatalytic Reaction.

Aqueous solutions containing both the strong oxidant, peroxydisulfate (S2O82-), and the strong reductant, oxalate (C2O42-), are thermodynamically unstable due to the highly exothermic homogeneous redox reaction: S2O82- + C2O42- → 2 SO42- + 2 CO2 (ΔG0 = -490 kJ/mol). However, at room temperature, this reaction does not occur to a significant extent over the time scale of a day due to its inherently slow kinetics. We demonstrate that the S2O82-/C2O42- redox reaction occurs rapidly, once initiated by the Ru(NH3)62+-mediated 1e- reduction of S2O82- to form S2O83•-, which rapidly undergoes bond cleavage to form SO42- and the highly oxidizing radical SO4•-. Theoretically, the mediated electrochemical generation of a single molecule of S2O83•- can initiate an autocatalytic cycle that consumes both S2O82- and C2O42- in bulk solution. Several experimental demonstrations of S2O82-/C2O42- autocatalysis are presented. Differential electrochemical mass spectrometry measurements demonstrate that CO2 is generated in solution for at least 10 min following a 30-s initiation step. Quantitative bulk electrolysis of S2O82- in solutions containing excess C2O42- is initiated by electrogeneration of immeasurably small quantities of S2O83•-. Capture of CO2 as BaCO3 during electrolysis additionally confirms the autocatalytic generation of CO2. First-principles density functional theory calculations, ab initio molecular dynamics simulations, and finite difference simulations of cyclic voltammetric responses are presented that support and provide additional insights into the initiation and mechanism of S2O82-/C2O42- autocatalysis. Preliminary evidence indicates that autocatalysis also results in a chemical traveling reaction front that propagates into the solution normal to the planar electrode surface.

Cellulosic ethanol stillage for methane production by integrating single-chamber anaerobic digestion and microbial electrolysis cell system

Anaerobic digestion provides a solution to the inefficient use of carbon resources caused by improper disposal of corn stover-based ethanol stillage (CES). In this regard, we developed a single-chamber anaerobic digestion integrated microbial electrolysis cells system (AD-MEC) to convert CES into biogas while simultaneously upgrading biogas in-situ by employing voltages ranging from 0 to 2.5 V. Our results demonstrated that applying 1.0 V increased the CH4 yield by 55 % and upgraded the CH4 content in-situ to 82 %. This voltage also promoted the well-formed biofilm on the electrodes, resulting in a 20-fold increase in current. However, inhibition was observed at high voltages (1.5–2.5 V), suppressing syntrophic organic acid-oxidizing bacteria (SOB). The dissociation between SOB and methanogens led to accumulation of propionic and butyric acid, which, in turn, inhibited methanogens. The degradation of CES was accelerated by unclassified_o_norank_c_Desulfuromonadia on the anode, likely leading to an increase in mixotrophic methanogenesis due to the synergistic interaction among Aminobacterium, Sedimentibacter, and Methanosarcina. Furthermore, the enrichment of electroactive bacteria (EB) such as Enterococcus and Desulfomicrobium likely facilitates direct interspecies electron transfer to Methanobacterium, thereby promoting the conversion of CO2 to CH4 through hydrogenotrophic methanogenesis. Rather than initially stimulating the EB in the bulk solution to accelerate the start-up process of AD, our study revealed that applying mild voltage up to 1.0 V tended to mitigate the negative impact on the original microorganisms, as it gradually enriched EB on the electrode, thereby enhancing biogas production.

Multilayer polyelectrolyte and palladium nanoparticle decorated porous materials as fixed-bed reactors for efficient reduction of 4-NP

In this study, a continuous flow catalytic reactor based on three-dimensional porous sponge bed with the uniform distribution of catalyst to treat 4-NP wastewater efficiently. The porous sponge is used as a support to construct polyelectrolyte multilayers by loading dopamine. And the multilayer polyelectrolyte is closely bound to dopamine to form polyelectrolyte film, and the nanocatalysts are synthesized by electrostatic adsorption of precursors. The reactor realizes the uniform and stable distribution of the catalyst in the three-dimensional porous sponge, and the reactant transfers from bulk solution to catalyst surface by the way of convection and diffusion, which enhances mass transfer and further improves the reaction efficiency. Under the operating conditions of a catalytic bed as small as 3 cm, a 4-NP concentration up to 4.5 mM, and a flow rate of 300 μL min−1, the conversion rate remained above 96 % for up to 200 h, indicating that the reactor has good catalytic efficiency. The results showed that this continuous flow catalytic system structure has excellent performance in wastewater treatment.

Bibliometric Study of Electrochemical Advanced Oxidation Processes (EAOPs) for Wastewater Treatment

Electrochemical advanced oxidation processes (EAOPs) are at the forefront of scientific research as green technologies aimed at effectively purifying polluted aquatic environments. These methods utilize electrochemical processes to generate reactive oxygen species (ROS), such as the hydroxyl radical (•OH), either on the anode surface or within the bulk solution, which can partially degrade or completely mineralize organic pollutants. The aim of the article is to provide a bibliometric analysis of research articles specifically focused on the application and development of EAOPs in wastewater treatment over the past five years. Utilizing the most extensive database for literature searches, Web of Science Core Collection (WoS), which encompasses 95% of global publications, a total of 649 research articles were retrieved by limiting the search results to words associated with EAOPs in titles, keywords, and abstracts. The bibliometric dataset was then processed using CiteSpace and VOSviewer software. The People’s Republic of China is emerging as the country with the highest production in the field, demonstrating a strong commitment to research and a leading role in international cooperation. This leadership is evident through China’s substantial contributions to the body of literature and its extensive network of collaborations with researchers worldwide. Meanwhile, Australia, despite producing fewer publications, has achieved a high citation rate, underscoring the significant impact and influence of its research within the scientific community. One of the most promising and extensively studied topics in this field is the electro-Fenton process, which has garnered considerable attention due to its potential applications and remarkable efficiency in various contexts. The bibliometric analysis conducted in this study allowed for a detailed visualization of the currently available literature data and corresponding developing trends. By mapping out the key areas of focus, prominent researchers, influential journals, and collaborative networks, this analysis provides valuable insights. These insights can facilitate future joint research endeavors, enhance collaboration, and promote the sharing of knowledge and best practices among researchers globally.