Mixed Solution Research Articles

Novel antimicrobial biodegradable composite films as packaging materials based on shellac/chitosan, and ZnAl2O4 or CuAl2O4 spinel nanoparticles.

ZnAl2O4 and CuAl2O4 spinel nanoparticles were prepared by a modified Pechini method and used with the natural chitosan (CS) and shellac (SH) polymers to form novel composite membranes as promising food packaging materials. The selection of ZnAl2O4 and CuAl2O4spinel nanoparticles was based on their antibacterial characteristics, availability, and economy. Using a straightforward and adaptable solution mixing and casting method, the bio-composites were created. The mechanical, physical, antibacterial, homogeneity and air permeability properties of composite films were investigated. The film structure was evaluated in terms of component interactions using FTIR spectra. The addition of 10% SH increased the tensile strength, percentage strain at maximum load, Young's modulus, and burst strength by 114-101%, 3.6-8.4, 103-119, and 179-153% for low and middle M.wt./CS respectively. Chitosan/shellac-CuAl2O4composite has superior properties compared to ZnAl2O4composite. In general, 0.05% spinel provides a composite having better qualities than that of 0.1 additions. Middle M.wt. chitosan provides a composite with superior properties compared to that of low M.wt. The incorporation of ZnAl2O4 or CuAl2O4 enhanced the thermal stability of the SH/CS composite. ZnAl2O4 provides superior thermal stability than CuAl2O4. When shellac/CS film structure is treated with the previously indicated ZnAl2O4 or CuAl2O4 formulation, the % swelling decreases along with an increasing in the gel fraction. The antimicrobial assessment using inhibition zone diameter and shake flask methods showed that a composite of 1:9 shellac/chitosan/0.05% of CuAl2O4 exerted the highest Gram-positive antibacterial activity against B. mycoides (21mm), and C. albicans (22mm). So, these enhancements make chitosan/shellac/ZnAl2O4 or CuAl2O4composite films a good alternative to producing food packaging materials.

Mixed Adsorption Mono- and Multilayers of ß-Lactoglobulin Fibrils and Sodium Polystyrene Sulfonate

The formation of beta-lactoglobulin (BLG)/sodium polystyrene sulfonate (PSS) complexes decelerates the change in the surface properties of the mixed solutions with the surface age and increases the steady-state dilational surface elasticity in a narrow PSS concentration range. At the same time, the changes in the surface properties are accelerated in the dispersions of BLG fibrils with and without PSS due to the influence of small peptides coexisting with fibrils. A decrease in the peptide concentration as a result of the dispersion purification leads to slower changes in the surface properties at low PSS concentrations. The increase in the polyelectrolyte concentration results in an increase in the steady-state surface elasticity due to the fibril/PSS complex formation and in very slow changes in the surface properties if the polyelectrolyte exceeds a certain critical value. The latter effect is a consequence of the formation of large aggregates and of an increase in the electrostatic adsorption barrier. The consecutive adsorption of BLG fibrils and PSS leads to the formation of regular multilayers at the liquid–gas interface. The multilayer properties change noticeably with an increase in the number of layers from four to six in agreement with previous results on the multilayers of PSS with an oppositely charged synthetic polyelectrolyte, presumably due to the heterogeneity of the first PSS layer. The dynamic elasticity of the multilayers approaches 250 mN/m, indicating that they can effectively stabilize foams and emulsions.

Development of pilot-scale plasma bubble reactors for efficient antibiotics removal in wastewater

Plasma bubble (PB) is a promising technology to control antibiotic wastewater pollution. However, the practical implementation of PB technology at the industrial-scale is still underdeveloped. In addition, the influence of different discharge modes for PB on wastewater treatment is largely unknown. This study designed pilot-scale PB reactors with different discharge modes to investigate the degradation effect of norfloxacin (NOR) and tetracycline (TC) in bulk tap water. Results indicate that the dielectric barrier discharge (DBD) mode with low average discharge power demonstrates superior degradation ability and higher production of O3(g) and .O2−(aq) compared to the spark mode which exhibits the high-intensity spark discharge in the tip area of the tube. After 40 min of treatment in a Double DBD reactor, 97.4% and 100% of NOR and TC are removed from 2 L tap water, attributed to the accumulation of antibiotic molecules by PBs and the in-situ generation of O3(g) and .O2−(aq) produced by plasma. Furthermore, a larger-scale PB reactor is developed by creating an array of four DBD reactors, effectively degrading 8 L mixed antibiotics solution. This study provides valuable insights for PB reactor design and the degradation performance of antibiotic wastewater, which will contribute to the further development of synergistic systems for plasma degradation.

Hydrogen bond, protonation, and coordination-induced supramolecular chirality inversion in glutamide-based amphiphilic self-assembly

In this study, we have synthesized two types of Y-shaped chiral amphiphiles, namely L-BG and L-PG, with a benzene or pyridine ring at the terminal position, respectively. The optimized conformations of both amphiphiles indicate the presence of intramolecular interactions. In dimethylformamide (DMF) solution at the monomeric state, both amphiphiles exhibit positive cotton effects; however, in DMF/H2O mixed solution, the cotton effects are inverted. Molecular dynamics simulations reveal that both intermolecular and intramolecular hydrogen bonds facilitate the inversion of supramolecular chirality. Additionally, protonation and coordination of L-PG assembly results in chirality inversion and transformation of emission. This study emphasizes the significance of both inter- and intramolecular hydrogen bonds in the assembly process, providing insights into stimuli-responsive chiral supramolecular materials.

Gas-liquid interface properties of fluorocarbon and hydrocarbon surfactants and their mixed foams: Molecular dynamics simulations and experimental studies

This paper focuses on the gas-liquid interface characteristics of short-chain fluorocarbon surfactant FS-50 and hydrocarbon surfactant sodium dodecyl sulfate (SDS) and their mixed systems. The foam properties of SDS, FS-50, and their mixed solutions were experimentally determined. Then, based on the molecular dynamics simulation method, the interaction mechanism of surfactant molecules at the gas-liquid interface was simulated and analyzed by constructing a foam-liquid membrane system containing surfactant molecules and water molecules. The experimental results show that FS-50 can effectively enhance the foam stability when the concentration is lower than 0.16 wt% and the mixing ratio with SDS is not more than 1:1; the simulation results show that FS-50 can change the arrangement of SDS molecules at the gas-liquid interface. Simultaneously, there is a competitive adsorption phenomenon between FS-50 and SDS at the gas-liquid interface. The low mixing ratio FS-50 can increase the thickness of the gas-liquid interface of the mixed system and the ability of SDS to form hydrogen bonds with water, enhance the water-locking ability of SDS, and further improve the stability of the foam liquid film. The interaction mechanism between short-chain fluorocarbons and SDS surfactants at the gas-liquid interface was revealed by simulation, which provided theoretical guidance for optimizing the performance of the foam liquid film.

A Portable Zn2+ Fluorescence Sensor for Information Storage and Bio-Imaging in Living Cells.

A fluorescence probe (Probe-ITR) was designed and synthesized for the rapid detection of Zn2+ based on the excited state intramolecular proton transfer (ESIPT) mechanism. The specific recognition ability of Probe-ITR to Zn2+ was tested using UV-VIS and fluorescence emission spectroscopy. The results demonstrated a rapid response within 40s upon addition of an appropriate amount of Zn2+ into the mixed solution of the target probe molecules (DMSO/PBS = 5/5). Under 365nm ultraviolet light irradiation, the colorless solution changed to yellow-green fluorescence with a 150-folds increase in intensity. Furthermore, the detection limit for specific recognition of Zn2+ by the probe molecule is only 17.3 nmol/L, indicating high sensitivity. The practical application potential of the probe molecules was enhanced by employing on information storage and conducting cell imaging experiments.

Elucidation of complexation mechanism of rosmarinic acid and berberine

Polyphenols are known to form complexes with various organic compounds. This ability can may change the chemical or physical properties of the compounds involved and may even affect their efficacy in the case of drugs. Our research revealed that mixing solutions of the polyphenol rosmarinic acid (RA) and berberine (Ber), a widely used and pharmacologically important isoquinoline alkaloid, resulted in the formation of a precipitate of the RA–Ber complex at a molar ratio of 1:1. This was confirmed using 1H NMR and Fourier Transform Infrared Spectroscopy. To elucidate the formation mechanism of the precipitate, the behavior of RA and Ber in an aqueous solution was examined using 1H NMR, indicating the formation of the RA–Ber complex at a molar ratio of 1:1, consistent with the results of precipitation. Additionally, we investigated the steric structure of the RA–Ber complex in an aqueous solution using molecular modeling calculations. These calculations suggested the existence of seven types different steric structures of the RA–Ber complex, primarily stabilized by π–π interactions. Based on these results, we concluded that mixing RA and Ber solutions in an aqueous environment results in the formation of RA–Ber complexes with seven types different steric structures at a molar ratio of 1:1. The precipitate forms because these complexes are less water-soluble than either RA or Ber alone.

Performance of Single Nanopore and Multi-Pore Membranes for Blue Energy.

The salinity gradient power extracted from the mixing of electrolyte solutions at different concentrations through selective nanoporous membranes is a promising route to renewable energy. However, several challenges need to be addressed to make this technology profitable, one of the most relevant being the increase of the extractable power per membrane area. Here, the performance of asymmetric conical and bullet-shaped nanopores in a 50 nm thick membrane are studied via electrohydrodynamic simulations, varying the pore radius, curvature, and surface charge. The output power reaches ~60 pW per pore for positively charged membranes (surface charge σw=160 mC/m2) and ~30 pW for negatively charges ones, σw=-160 mC/m2 and it is robust to minor variations of nanopore shape and radius. A theoretical argument that takes into account the interaction among neighbour pores allows to extrapolate the single-pore performance to multi-pore membranes showing that power densities from tens to hundreds of W/m2 can be reached by proper tuning of the nanopore number density and the boundary layer thickness. Our model for scaling single-pore performance to multi-pore membrane can be applied also to experimental data providing a simple tool to effectively compare different nanopore membranes in blue energy applications.

Guanidinium‐Based Covalent Organic Framework Membranes for Superior Mono‐ and Divalent Cations Separation

Biological membranes exhibit extraordinary efficiency in processing ion permeability and selectivity. However, creating artificial membranes for an ideal ion separation is still challenging due to the subtle distinctions in valence and size among different ions. In the realm of biological recognition, the ultimate selectivity of ion channels is considered to stem from the specific binding interactions and appropriate charge density. Designing artificial membranes to achieve similar performance not only helps the understanding of complex ion transport in bioprocesses but also facilitates critical industrial separations. Inspiring by the remarkable performance in biological systems, a guanidinium‐based covalent organic framework membrane is designed, which exhibits an excellent capability to recognize mono‐/divalent cations, achieving K+/Mg2+ selectivity up to 202 in a mixed salt solution. Furthermore, the membrane displays rapid ion transport owing to the uniform sub‐2 nm channels. The experimental results and molecular dynamics simulations illustrate that the charge‐assisted hydrogen bonding sites and the Cl− counter ions within 1D channels play critical roles in cations sieving. Specifically, divalent ions passing through the positively charged channels need to overcome higher energy barriers than monovalent ions. These findings offer promising avenues for the development of advanced multifunctional membranes for efficient ion separation and sustainable water‐related separations.

Injectable nanocomposite hydrogel with cascade drug release for treatment of uveal melanoma

Uveal melanoma (UM) is the most common malignant intraocular tumor with the trait of distant metastases. Currently, the standard clinical therapy results in suboptimal outcomes due to ineffective inhibition of tumor metastasis. Thus, developing novel therapeutic modalities for UM remains a critical priority. Herein, we have developed an injectable nanocomposite hydrogel (HA-DOX/LAP gel) through integrating hyaluronic acid-based drug-loaded nanoparticles into an alginate-dopamine gel, delivering the chemotherapeutic drugs, lapatinib and doxorubicin for combinational treatment of UM. HA-DOX/LAP gel is fabricated in situ by a simple injection of the mixed precursor solution into tumor sites and maintains in vivo for more than 21 days. The entrapped drug-loaded nanoparticles can gradually release from HA-DOX/LAP gel, enhancing tumor targeting and penetration, and synchronously releasing lapatinib and doxorubicin into the acidic intracellular environment to synergistically destroy UM cells. In vivo anti-tumor studies conducted in MuM-2B tumor models demonstrated that HA-DOX/LAP gel significantly impedes tumor growth, diminishes postoperative recurrence, and prolongs overall survivals of UM tumor-bearing mice through only single injection. Remarkably, the escaped drug-loaded nanoparticles effectively reduce the risk of tumor metastases. Our findings provide new insights for the development of multifunctional nanocomposite-incorporating combination therapy against UM by targeting tumor recurrence and metastases.

Efficient separation and recovery of cobalt from grinding waste of cemented carbide using a sulfuric acid-sodium persulfate mixed solution

The mechanical processing of cemented carbide often generates a considerable amount of grinding waste from cemented carbide (GWCC), which serves as an important secondary resource for recovering Co and W. However, efficient separation of tungsten carbide (WC) and Co from GWCC remains challenging. This study tested an efficient process for separating Co from GWCC using a mixed solution of H2SO4-Na2S2O8. Under optimum conditions of 20 g/L H2SO4, 30 g/L Na2S2O8, 60 °C, and 1 h, the leaching efficiency of Co reached 97.0 %, compared to only 58.6 % when using H2SO4 alone. The kinetics of Co leaching in H2SO4 and H2SO4-Na2S2O8 solutions were determined to be a combination of chemical reaction control and diffusion control, suggesting that Co leaching rate in H2SO4 solution is significantly enhanced by introducing Na2S2O8. Finally, complete recovery of Co was achieved, and pure Co powder with a flower-cluster morphology was prepared from the leaching solution through oxalic acid precipitation followed by vacuum pyrolysis. The regenerative WC and Co powder can be recycled for cemented carbide production.

Impact of pH-Dependent Dynamics of Human Serum Proteins on Dialysis Membranes: Cryptographic Structure Assessment, Synchrotron Imaging of Membrane-Protein Adsorption, and Molecular Docking Studies

Proteins are fundamental to biochemical processes and critical in hemodialysis. This study investigates the impact of pH on human serum albumin (HSA), fibrinogen (FB), and transferrin (TRF) interactions with polyarylethersulfone (PAES) hemodialysis membranes. A multi-method approach was utilized, including protein crystallography for structural insights, hydration layer analysis to explore solvation and interaction potentials, molecular docking using AutoDock 4.0 for binding affinity simulations, and in-situ X-ray synchrotron SR-μCT imaging to observe protein deposition dynamics.Molecular docking revealed that PAES demonstrated superior binding energies and interaction patterns with FB and TRF compared to cellulose triacetate (CTA), facilitated by specific hydrogen bonding within a water shell. CTA displayed weaker, hydration-sensitive interactions varying with pH. Imaging studies indicated that FB showed higher adsorption at pH 6 than at pH 7.2, predominantly in the middle membrane regions. Similarly, HSA and TRF exhibited increased adsorption at pH 6, suggesting a stronger affinity under acidic conditions. Mixed protein solutions also indicated higher adsorption at pH 6, emphasizing an increased risk of membrane fouling.These findings highlight the crucial role of pH in modulating protein-membrane interactions and enhancing the efficacy of hemodialysis. A deeper understanding of hydration environments and their effects on protein binding affinities provides valuable insights for optimizing membrane design and performance. Clinically, this research suggests that fine-tuning pH during hemodialysis could mitigate protein fouling on membranes, thereby improving procedural efficiency and potentially leading to better patient outcomes through enhanced dialysis effectiveness.

Dicarboxylate cellulose nanofibrils-supported silver nanoparticles as a novel, green, efficient and recyclable catalyst for 4-nitrophenol and dyes reduction

This study reports dicarboxylate cellulose nanofibrils (DCNF) as a novel reducing and supporting agent for producing silver nanoparticles (AgNPs) with high efficiency (63.82 % reduction) and loading (6.88 %) using UV light. Unlike previous research, AgNPs formation with DCNF doesn't involve cellulose oxidation. Instead, it appears to involve a loss of carboxyl groups from DCNF. In comparative studies, pristine CNF (PCNF) and TEMPO-oxidized CNF (TOCNF) were also examined for AgNPs production. The resulting AgNPs from DCNF exhibited a significantly smaller average size (3.9 ± 0.7 nm) compared to those from PCNF (26.9 ± 10.9 nm) and TOCNF (13.5 ± 4.5 nm). Catalytic activity evaluation by the 4-nitrophenol (4-NP) reduction reaction revealed a high rate constant of 8.47× 10−3 s−1 by AgNPs/DCNF, which surpassed AgNPs/TOCNF (1.79 × 10−3 s−1) and AgNPs/PCNF (0.63 × 10−3 s−1) by 4.7 and 13.4 times, respectively. Besides 4-NP, AgNPs/DCNF aerogels were also applied for methyl orange and Rhodamine B dyes reduction. The aerogels showed excellent reusability, maintaining over 95 % conversion even after five cycles and also effective in treating real samples and mixed dye solutions. This study opens the door for future research exploring DCNF as a support material for various metal, metal oxide, and carbon nanoparticles.

Novel sol-gel derived layered double oxides and layered double oxide/γ-Al2O3 with tunable selectivity as promising adsorbents for L-lactate uptake from the myoblast culture medium

Cultured meat production, a biotechnological solution for global protein demand and sustainability, faces economic challenges due to the high demand for cell culture medium. Contamination with cell metabolites, particularly L-lactate, impedes myoblast proliferation in high-density suspension culture. Eliminating L-lactate is crucial for reusing the medium and overcoming economic barriers in mass myoblast culture. Retaining essential nutrients like D-glucose, amino acids, and vitamins after L-lactate removal is imperative for sustained myoblast growth. This study proposes a sustainable and economically feasible adsorption technique utilizing novel sol-gel derived Mg-Al layered double oxides and Mg-Al layered double oxide/γ-Al2O3 with tunable selectivity as a promising tool for L-lactate uptake from the myoblast medium. In an aqueous solution, L-lactate uptake and selectivity over D-glucose were enhanced with the decrease in total Mg/Al ratio and crystallinity, increase in Al2O3 dispersion in adsorbent, specific surface area, and porosity. The latter was achieved successfully by metal alkoxide sol-gel method employing an organic structure-directing agent, where LDO/amorphous alumina nanohybrid with Mg/Al = 1.23 was successfully prepared in mixed methanol-ethanol solution in a relatively short time. A simple mixture of Mg-Al LDO with Mg/Al = 2 and nano-γ-Al2O3 prepared by a sustainable and economically feasible co-precipitation method was found to have comparable efficiency and selectivity to a costly sol-gel derived material. In myoblast medium, lower total Mg/Al was associated with higher cytocompatibility, pH-stability, and selectivity, while surface properties of materials did not play a significant role. Nano-γ-Al2O3 was identified as the most promising material for selective L-lactate uptake from the myoblast culture medium. Thus, further optimization of the medium treatment process with nano-γ-Al2O3 can realize cost-effective high-density myoblast culture with circular use of the medium – a novel sustainable process in the biotechnology field.

Strengthening Resilience and Sustainability for Post-Disaster Recovery: A Comparative Law and Economics Analysis on Smart Mixes Between Mechanisms

This article advocates smart mixes of mechanisms of post-disaster recovery in terms of boosting resilience and sustainability through liability rules, government intervention, insurance, and their combinations. Liability rules can provide compensation to victims and, in theory, also reduce disaster risks, while they have their limits in practice. The government widely intervenes in disaster compensation in many countries, but it faces challenges in how it can intervene fairly and efficiently, whether through informal channels, such as ad hoc charity, or structured approaches, such as compensation funds. As governments may struggle to provide efficient and effective compensation ex post, insurance may offer proactive solutions with models of first-party catastrophe insurance and third-party liability insurance ex ante. Where market failure, liability failure, and government failure may all arise, a smart mix of mechanisms is often preferable from a law and economic perspective, rather than relying solely on one framework. However, upon examining empirical evidence regarding the effectiveness of these instruments in China, the UK, France, Germany, and Turkey, it becomes apparent that a mix of mechanisms is not always applied in an effective manner. Models of mandatory comprehensive disaster insurance, and Public–Private Partnership (PPP), which both receive government intervention as a last resort to the market and liability failures, can reach the goal of more effective compensation for disaster victims, risk prevention and resilience when faced with disaster recovery, and should therefore be substantially implemented beyond the current levels. To be clear, the proposed mix of solutions mainly focuses on legal and economic dimensions which are rather limited, ignoring, for example, building codes for structures and physical interventions.

Ion Identification and Ultralow Concentration Sensing with Liquid Flexoelectricity.

The isolation and concentration of electrical charges at ionic-electronic interfaces are prevalent phenomena that impede effective communication between ionic and electronic systems. Detecting these concentrated charges at the interface is crucial for applications, such as signal transmission and ion detection. Current electrical detection approaches introduce additional ionic-electronic interfaces via metallic electrodes with an external stimulating voltage, which alters the initial ion distributions at the interfaces. In this work, we introduce the flexoelectricity of liquids to examine the electrical charge aggregation at ionic-electronic interfaces under cyclic mechanical loads. The measured electrical responses reflect the coupling phenomena between the flexoelectricity and the electric double layer. This proposed approach demonstrates the capability to quantify ion types and concentrations at interfaces. Furthermore, it can identify ion types in mixed solutions and offers high sensitivity at ultralow concentrations. This work promotes a nonchemical, general mechanical method for charge detection at ionic-electronic interfaces.

Optimizing the surface quality of electrochemical machined Ni-based single crystal superalloy via manipulation of phase and dendrite dissolution

The transpassive dissolution behaviors of Ni-based single crystal superalloy in 10 %NaCl, 10 %NaNO3, and mixed solution are investigated by using potentiodynamic polarization, scanning electron microscopy, energy dispersive X-ray spectroscopy, and X-ray photoelectron spectroscopy. The alloy exhibits opposite yet complementary dissolution characteristics in NaCl and NaNO3 solutions. The different responses of γ/γ′ phases to Cl− and NO3− contribute to the opposite dissolution behaviors of dendrites and interdendritic regions. The surface flatness is noticeably enhanced in mixed solution due to the synchronous dissolution of the γ/γ′ phases. Our work paves the way for obtaining high-quality surface in electrochemical machining of single crystal superalloys.

Consumer liking of steamed green Chinese cabbage (Brassica rapa ssp. chinensis) cultivated in formulated vegetable waste-based organic hydroponic solutions

Chinese cabbage or pak choy (Brassica rapa ssp. chinensis) is often consumed because of its high nutritional content and several health advantages. Due to their promotion as being healthier and more ecologically friendly, hydroponic vegetables have seen a recent spike in consumer interest. The production of Chinese cabbage involved the processing of the vegetable waste to create various hydroponic solution formulations (F1 = banana peels, eggshells, and bean sprouts; F2 = banana humps, onion peels, bean sprouts, and moringa leaves; F3 = moringa leaves, onion peels, and bean sprouts; and F4 = AB Mix solution). They were applied at concentrations of 600, 900, 1,200, and 1,500 parts per million. The aim of this study was to investigate the relationship between the type of hydroponic growth solutions and Chinese cabbage customer acceptance. As a result, using a hedonic test of consumer liking, a panel of 32 untrained individuals was asked to show their liking score on sensory attributes of Chinese cabbage. There was a significant difference in the color liking of Chinese cabbage as an effect of hydroponic solution formulation. However, both organic vegetable waste-based formulations did not statistically substantially affect consumer acceptance, which includes color, taste, flavor, texture, and overall liking. Ultimately, vegetable waste-based organic formulations can be used to produce Chinese cabbage that is as acceptable to customers as those prepared with inorganic AB-Mix solution.

Insights into mixed dye pollutant degradation by oxygen and air plasma bubbling array

Abstract Synthetic organic dye pollutants pose a serious threat to the aquatic ecological environment due to their difficulty in complete degradation. This study employed a plasma bubble array reactor to degrade individual and mixed dye pollutant solutions of Sunset Yellow (SY), Methyl Orange (MO), and Methyl Violet (MV). The degradation efficiencies and mechanisms of the plasma were investigated under different working gas atmospheres. It was found that oxygen plasma degraded the target dyes and their mixtures more significantly than air plasma. Specifically, compared with air plasma, the removal of single dyes SY, MO and MV by oxygen plasma was increased by 76.6%, 13.8% and 3%, respectively, after 20 min of treatment. As for mixed dyes, after 25 min treatment, oxygen plasma removed 99.1%, which was 31.6% higher than air plasma. However, the degradation kinetic order in oxygen plasma was SY > MO > MV, while that in air plasma was MV > MO > SY. Combined with the detection of reactive oxygen-nitrogen species (RONS), the results showed that the reactive oxygen species (ROS) played an important role in the degradation of SY, and it was also important for the degradation of MO, whereas both the ROS and reactive nitrogen species (RNS) were important for the degradation of MV. Scavenger experiments revealed that hydroxyl (·OH) and superoxide anion (·O2-) played the most important roles in the degradation process. The three dyes were basically completely degraded within 14-20 minutes of treatment, with corresponding yields of 1.94-2.79 g/kWh. Possible degradation pathways for each dye were deduced based on LC-MS and the toxicities of solutions were evaluated by phytotoxicity tests and ion chromatography. The results showed that the biotoxicity of the intermediates was significantly reduced. This study may provide a feasible option for effective application of plasma technology in organic dye wastewater treatment.

Skill mix among healthcare workers during the Covid-19 pandemic – a scoping review

Abstract Background The problem of human resource shortages in health care was highlighted during the Covid-19 pandemic in many countries around the world. Various solutions have been implemented to cope with the crisis, one of which is the skill mix of medical and peri-medical staff. The aim of the scoping review was to systematise knowledge about the skill mix of healthcare workers during the Covid-19 pandemic. Methods The review was conducted in five scientific databases including Cinahl Ultimate, Web of Science, Medline (PubMed), Embase and Scopus. The review included studies published from 2020 until July 2023, presenting original research on the skill mix of health care workers. Results A total of 5039 records were identified in the databases and 27 articles were included in the final analysis. Of the included studies, 14 were conducted in Western and Southern Europe. Most of the studies included in the review were conducted among nurses (n = 12), pharmacists (n = 11) and doctors (n = 6). The majority of studies concerned re-allocating tasks (n = 9) and re-allocating tasks and introducing or changing teamwork (n = 7). Research covered psychological aspects of work, patient safety, work reorganisation and training and collaboration. Many studies also focused on difficulties and barriers related to skill mix, such as blurring of responsibilities and role ambiguity. The review did not identify any studies conducted among laboratory diagnosticians, medical coordinators or surgical assistants. In addition, there were no studies of skill mix in Central and Eastern Europe during the pandemic. Conclusions Given that skill mix may be one of the solutions to reduce the negative impact of staff shortages, more research should be conducted in this area. Healthcare professionals should be involved in decision-making processes related to the granting of new competencies or the creation of new professions/functions in healthcare. Key messages • It is necessary to involve health professionals in the process of creating new skill mix solutions. • More research is needed on skill mix in times of crisis, particularly in Central and Eastern Europe.