Ethylenediaminetetraacetic Acid Disodium Research Articles

With Blue Light against Biofilms: Berberine as Natural Photosensitizer for Photodynamic Inactivation of Human Pathogens

Evolving antibiotic resistance of bacteria is a prevailing global challenge in health care and requires the development of safe and efficient alternatives to classic antibiotics. Photodynamic Inactivation (PDI) has proven to be a promising alternative for treatment of a broad range of microorganisms. Photodynamic Inactivation uses photoactive molecules that generate reactive oxygen species (ROS) upon illumination and in the presence of oxygen, which immediately kill pathogenic target organisms. Relevant photoactive properties are provided by berberine. Originally extracted from Barberry (Berberis vulgaris), it is a natural compound widely used in Traditional Chinese Medicine for its antimicrobial and anti-inflammatory effects. With this study, we demonstrated the potential of berberine chloride hydrate (Ber) as a photosensitizer for PDI of important human pathogens, Gram(+) Staphylococcus capitis subsp. capitis, Gram(+) Staphylococcus aureus, and Gram(−) Escherichia coli. In vitro experiments on planktonic and biofilm cultures were conducted focusing on Ber activated with visible light in the blue wavelength range. The number of planktonic S. capitis cells was reduced by 7 log10 steps using 100 µM Ber (5 min incubation, illumination with 435 nm LED array, radiant exposure 25 J/cm2). For an antibacterial effect of 4 log10 steps, static S. capitis biofilms required 1 mM Ber, a drug-to-light interval of 60 min, and illumination with 100 J/cm2. Almost all planktonic cells of Staphylococcus aureus could be photokilled using 100 µM Ber (drug-to-light interval of 30 min, radiant exposure 25 J/cm2). Biofilms of S. aureus could be phototreated (3 log10 steps inactivation) when using 1 mM Ber incubated for 5 min and photoactivated with 100 J/cm2. The study is highlighted by the proof that PDI treatment using Ber showed an antibacterial effect on Gram(−) E. coli. Planktonic cells could be reduced by 3 log10 steps with 100 µM Ber (5 min incubation, 435 nm, 25 J/cm2). With 5 mM ethylenediamine tetraacetic acid disodium salt dihydrate (Na2EDTA) or 1.2% polyaspartic acid (PASA) in addition, a relative inactivation of 4 log10 steps and 7 log10 steps, respectively, was detectable. Furthermore, we showed that an antibacterial effect of 3.4 log10 towards E. coli biofilms was given when using 1 mM Ber (5 min incubation, 435 nm, 100 J/cm2). These results underscore the significance of PDI-treatment with Ber as a natural compound in combination with blue light as valuable antimicrobial application.

Indium Tin Oxide Induced Internal Positive Feedback and Indium Ion Transport in Perovskite Solar Cells.

Stability is the most pressing challenge hindering the commercialization of perovskite solar cells (PSCs), and previous efforts focused more on enhancing the resistance of PSCs to external stimulus. Here, we found that the indium tin oxide (ITO) will deteriorate the photovoltaic performance of PSCs through positive feedback cycles. Specifically, the perovskite degradation products will cross the electron transport layer to chemically etch the electrode ITO to generate In3+, which will migrate upwards into the perovskite film. Then, the reaction that corrodes ITO consumes the decomposition products of perovskite and shifts the balance of the perovskite decomposition reaction, further promoting the degradation and thus falling into a positive feedback cycle. Moreover, the In3+ in the perovskite film was found to accumulate at the upper surface, which would lead to n-type doping of perovskite film to form the energy barrier for interface carrier extraction. Subsequently, the chelating molecule ethylenediaminetetraacetic acid disodium salt (EDTA-2Na) was introduced onto ITO to firmly chelate the In3+ and prevent it from migrating upward, thus breaking this internal positive feedback cycle and significantly enhancing the efficiency and stability of PSCs. This work provides new perspectives for understanding the mechanism of photovoltaic performance loss and ionic transport in PSCs.

Indium Tin Oxide Induced Internal Positive Feedback and Indium Ion Transport in Perovskite Solar Cells

AbstractStability is the most pressing challenge hindering the commercialization of perovskite solar cells (PSCs), and previous efforts focused more on enhancing the resistance of PSCs to external stimulus. Here, we found that the indium tin oxide (ITO) will deteriorate the photovoltaic performance of PSCs through positive feedback cycles. Specifically, the perovskite degradation products will cross the electron transport layer to chemically etch the electrode ITO to generate In3+, which will migrate upwards into the perovskite film. Then, the reaction that corrodes ITO consumes the decomposition products of perovskite and shifts the balance of the perovskite decomposition reaction, further promoting the degradation and thus falling into a positive feedback cycle. Moreover, the In3+ in the perovskite film was found to accumulate at the upper surface, which would lead to n‐type doping of perovskite film to form the energy barrier for interface carrier extraction. Subsequently, the chelating molecule ethylenediaminetetraacetic acid disodium salt (EDTA‐2Na) was introduced onto ITO to firmly chelate the In3+ and prevent it from migrating upward, thus breaking this internal positive feedback cycle and significantly enhancing the efficiency and stability of PSCs. This work provides new perspectives for understanding the mechanism of photovoltaic performance loss and ionic transport in PSCs.

In Situ Modification of Activated Carbon Made from Camellia oleifera Shell with Na2EDTA for Enhanced La3+ Recovery

It is important to recover La3+ from metallurgical solutions or wastewater. However, the recovery rate of La3+ is usually less than 1% and the recovery methods are not environmentally friendly or user-friendly. Therefore, a straightforward, efficient, clean, and economically friendly method is needed. In this investigation, a modified adsorbent, COSAC-Na2EDTA-15, which was made from the Camellia oleifera shell (COS) and disodium ethylenediaminetetraacetic acid (Na2EDTA), was invented. In addition, characterization of the COSAC-Na2EDTA-15 adsorbent was conducted using SEM and XPS, and the principle of adsorption was revealed. The adsorption kinetics followed P-S-O KM, while the isotherm of COS-activated carbon (COSAC) aligned more closely with the Langmuir model. Compared to COSAC, the maximum La3+ adsorption capacity of COSAC-Na2EDTA-15 increased from 50 to 162.43 mg/g, and the content of O and N changed from 7.31% and 1.48% to 12.64% and 4.15%, respectively. The surface of the COSAC-Na2EDTA-15 exhibited abundant C, N, and O elements, and La3+ was detected on the sample surface after adsorption. The test and analysis results fully indicate that La3+ can be successfully adsorbed on the surface of COSAC-Na2EDTA-15. Because of its easy preparation, low cost, and superior performance, activated carbon made from COS finds extensive applications in the adsorption and recovery of rare earth elements.

Rechargeable zinc-water battery for sustainable hydrogen generation

Metal-water primary batteries hold promise for distributed hydrogen production but suffer from limited renewability of metal electrodes in aqueous electrolytes. Here, we introduce a novel concept of a rechargeable zinc-water battery featuring a reversible zinc anode paired with a bifunctional water electrolysis electrode, realized in a specially designed aqueous electrolyte-a mild zinc triflate aqueous electrolyte with the addition of ethylenediaminetetraacetic acid disodium (EDTANa2). The system enables high-purity hydrogen production during discharge and high-purity oxygen production during charge in a membrane-free setup. In the zinc-water battery, EDTANa2 enhances the water-splitting electrode's performance by replacing hydrophobic OTF- anions, ensuring optimal water activity. Additionally, EDTANa2 enhances Zn electrode reversibility by chelating Zn2+, preventing solvated water decomposition during zinc deposition. This integrated battery continuously undergoes charge-discharge cycles for over 55 h at a current density of 6 mA cm-2. Moreover, it achieves a high hydrogen evolution rate of 12.5 mL cm-2 h-1, enabling cost-effective, high-purity hydrogen production without expensive membranes. These findings open new avenues for sustainable hydrogen generation and energy storage in nano energy systems.

Improved UV stability of perovskite devices based on the synergistic effect of electron layer passivation engineering and component engineering

The electron transport layer is one of the key factors in constructing high-performance perovskite solar cells (PSCs). Pb2+ reduction induced by ultraviolet light can cause the generation of vacancies and defects, leading to the degradation of perovskite films and the reduction of PSCs performances. Ethylenediamine tetraacetic acid disodium salt (EDTA) is a chelating agent that can bind to Sn2+ divalent metal ions and hence change material properties. Herein, EDTA-SnO2/CeO2 composite electron transport layers were constructed to improve the ultraviolet light stability of PSCs. The oxygen defect in electron layers of tin dioxide could be passivated by the surface of EDTA; whilst rod-like CeO2 was used as a mesoporous electron transport layer and UV shielding agent, which can reflect UV light and prevent the absorption layer from being damaged. CeO2 has also a suitable band gap; this accelerates the charge extraction and transfer, suppresses the recombination of interfacial carriers. The experimental results showed that the ultraviolet light stability of PSCs was significantly improved. After continuous irradiation of ultraviolet light with energy of 80 mW/cm2 for 12 h, the unencapsulated device with CeO2 maintained nearly 90% the initial efficiency.

Simultaneous determination of 31 banned veterinary drugs during egg-laying period in poultry eggs by ultra performance liquid chromatography-tandem mass spectrometry

The consumption of poultry eggs has increased in recent years owing to the abundance of production and improvements in living standards. Thus, the safety requirements of poultry eggs have gradually increased. At present, few reports on analytical methods to determine banned veterinary drugs during egg-laying period in poultry eggs have been published. Therefore, establishing high-throughput and efficient screening methods to monitor banned veterinary drugs during egg-laying period is imperative. In this study, an analytical method based on ultra performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) combined with QuEChERS-based techniques was developed for the simultaneous determination of 31 banned veterinary drugs encompassing nine drug classes (macrolides, antipyretic and analgesic drugs, sulfonamides, antibacterial synergists, anticoccidials, antinematodes, quinolones, tetracyclines, amphenicols) in different types of poultry eggs. The main factors affecting the response, recovery, and sensitivity of the method, such as the extraction solvent, purification adsorbent, LC separation conditions, and MS/MS parameters, were optimized during sample pretreatment and instrumental analysis. The 31 veterinary drug residues in 2.00 g eggs were extracted with 2 mL of 0.1 mol/L ethylene diamine tetraacetic acid disodium solution and 8 mL 3% acetic acid acetonitrile solution, and salted out with 2 g of sodium chloride. After centrifugation, 5 mL of the supernatant was cleaned-up using the QuEChERS method with 100 mg of octadecylsilane-bonded silica gel (C18), 50 mg of N-propylethylenediamine (PSA), and 50 mg of NH2-based sorbents. After nitrogen blowing and redissolution, the 31 target analytes were separated on a Waters CORTECS UPLC C18 analytical chromatographic column (150 mm×2.1 mm, 1.8 μm) at a flow rate, column temperature, and injection volume of 0.4 mL/min, 30 ℃, and 5 μL, respectively. Among these analytes, 26 analytes were acquired in dynamic multiple reaction monitoring (MRM) mode under positive electrospray ionization (ESI+) conditions using (A) 5 mmol/L ammonium acetate (pH 4.5) and (B) acetonitrile as mobile phases. The gradient elution program was as follows: 0-2.0 min, 12%B-30%B; 2.0-7.5 min, 30%B-50%B; 7.5-10.0 min, 50%B; 10.0-10.1 min, 50%B-100%B; 10.1-12.0 min, 100%B; 12.0-12.1 min, 100%B-12%B; The five other target analytes were acquired in MRM mode under negative electrospray ionization (ESI-) conditions using (A) H2O and (B) acetonitrile as mobile phases. The gradient elution program was as follows: 0-2.0 min, 12%B-40%B; 2.0-6.0 min, 40%B-80%B; 6.0-6.1 min, 80%B-100%B; 6.1-8.0 min, 100%B; 8.0-8.1 min, 100%B-12%B. Matrix-matched external standard calibration was used for quantification. The results showed that all the compounds had good linear relationships within their respective ranges, with correlation coefficients of >0.99. The limits of detection (LODs) and quantitation (LOQs) were 0.3-3.0 μg/kg and 1.0-10.0 μg/kg, respectively. The average recoveries of the 31 banned veterinary drugs spiked at three levels (LOQ, maximum residue limit (MRL), and 2MRL) in poultry eggs ranged from 61.2% to 105.7%, and the relative standard deviations (RSDs) ranged from 1.8% to 17.6%. The developed method was used to detect and analyze banned veterinary drugs in 30 commercial poultry egg samples, including 20 eggs, 5 duck eggs, and 5 goose eggs. Enrofloxacin was detected in one egg with a content of 12.3 μg/kg. The proposed method is simple, economical, practical, and capable of the simultaneous determination of multiple classes of banned veterinary drugs in poultry eggs.

Achieving strong interfacial bonding of CFRP and magnesium alloy by modifying magnesium alloy surface via alkaline etching with EDTA addition

The interfacial properties of fibre metal laminates are closely related to the surface microstructure of metals. Herein, a hitherto unreported honeycomb-like micro/nano-porous structure was successfully fabricated on an AZ31B Mg alloy surface by incorporation of ethylenediaminetetraacetic acid disodium (EDTA-2Na) into an alkaline solution and achieved excellent interfacial bonding property between AZ31B and carbon fibre-reinforced plastic. The addition of EDTA-2Na can promote the formation of etched pores. The growing nano-scale etched pores join together to produce micro-scale pores and ultimately lead to the formation of a micro/nano-porous structure. The 60 min etched AZ31B/carbon fibre-reinforced plastic laminate exhibits a bonding strength of 25.87 MPa, which is an increase of 350.7% compared to that of the untreated sample. The significant increase in bonding strength is mostly ascribed to composite mechanical interlocking by the micro/nano-porous structure and chemical bonding through the formation of MgCO3 and MgO1+X. In addition, the characteristics of micro-pores also affect the bonding strength.

Time-dependent hormesis transfer from five high-frequency personal care product components to mixtures

There is potential for personal care products (PCPs) components and mixtures to induce hormesis. How hormesis is related to time and transmitted from components to mixtures are not clear. In this paper, we conducted determination of components in 16 PCP products and then ran frequent itemset mining on the component data. Five high-frequency components (HFCs), betaine (BET), 1,3-butanediol (BUT), ethylenediaminetetraacetic acid disodium salt (EDTA), glycerol (GLO), and phenoxyethanol (POE), and 14 mixtures were identified. For each mixture system, one mixture ray with the actual mixture ratios in the products was selected. Time-dependent microplate toxicity analysis was used to test the luminescence inhibition toxicity of five HFCs and 14 mixture rays to Vibrio qinghaiensis sp.-Q67 at 12 concentration gradients and eight exposure times. It is showed that BET, EDTA, POE, and 13 mixture rays containing at least one J-type component showed time-dependent hormesis. Characteristic parameters used to describe hormesis revealed that the absolute value of the maximum stimulatory effect (|Emin|) generally increased with time. Notably, mixtures composed of POE and S-type components showed greater |Emin| than POE alone at the same time. Importantly, the maximum stimulatory effective concentration, NOEC/the zero effective concentration point, and EC50 remained relatively stable. Nine hormesis transmission phenomena were observed in different mixture rays. While all mixtures primarily exhibited additive action, varying degrees of synergism and antagonism were noted in binary mixtures, with no strong synergism or antagonism observed in ternary and quaternary mixtures. These findings offer valuable insights for the screening of HFCs and their mixtures, as well as the study of hormesis transmission in personal care products.

Dual-Responsive Hydrogels for Mercury Ion Detection and Removal from Wastewater.

This study describes the development of a fast and cost-effective method for the detection and removal of Hg2+ ions from aqueous media, consisting of hydrogels incorporating chelating agents and a rhodamine derivative (to afford a qualitative evaluation of the heavy metal entrapment inside the 3D polymeric matrix). These hydrogels, designed for the simultaneous detection and entrapment of mercury, were obtained through the photopolymerization of 2-acrylamido-2-methyl-1-propanesulfonic acid (AMPSA) and N-vinyl-2-pyrrolidone (NVP), utilizing N,N'-methylenebisacrylamide (MBA) as crosslinker, in the presence of polyvinyl alcohol (PVA), a rhodamine B derivative, and one of the following chelating agents: phytic acid, 1,3-diamino-2-hydroxypropane-tetraacetic acid, triethylenetetramine-hexaacetic acid, or ethylenediaminetetraacetic acid disodium salt. The rhodamine derivative had a dual purpose in this study: firstly, it was incorporated into the hydrogel to allow the qualitative evaluation of mercury entrapment through its fluorogenic switch-off abilities when sensing Hg2+ ions; secondly, it was used to quantitatively evaluate the level of residual mercury from the decontaminated aqueous solutions, via the UV-Vis technique. The ICP-MS analysis of the hydrogels also confirmed the successful entrapment of mercury inside the hydrogels and a good correlation with the UV-Vis method.

Degradation of Organic Dyes by the UCNP/h-BN/TiO2 Ternary Photocatalyst.

In this study, upconversion nanoparticles (UCNPs) with a flower-like morphology were prepared using a urea coprecipitation method. A ternary photocatalyst was first prepared using a solvothermal method involving the use of titanium oxide (TiO2), hexagonal boron nitride (h-BN), and UCNPs (Y2O3, Yb3+, and Tm3+) as raw materials. The surface morphology, crystal structure, and functional groups of these materials were then characterized and analyzed through scanning electron microscopy, transmission electron microscopy, X-ray diffraction analysis, Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, ultraviolet-visible spectrophotometry, and other techniques. Photocatalytic experiments were also conducted to investigate the effects of different catalyst types, raw material doping ratios, pH values, and catalyst quantities on the photocatalytic degradation of rhodamine B (RhB). The results indicated that doping with h-BN and UCNPs reduced the band gap width of RhB, increased its light absorption rate, and decreased the recombination rate of its photogenerated electrons and holes so that the photocatalytic degradation effect reached 100% within 2 h. After five experimental cycles, the 30% UC-BN-Ti photocatalyst remained highly durable and stable. To investigate the effects of different trapping agents on the degradation of RhB, benzoquinone, isopropanol, and ethylenediaminetetraacetic acid disodium salt were used as free-radical-capturing agents. The results indicated that •O2- was the primary active species in the degradation process. Finally, the pathway and mechanism of the degradation of RhB through ternary composite photocatalysis were identified.

Extraction of Soluble Salts and Iron Sulfides from the Wood of the “Huaguangjiao I” Shipwreck

Shipwreck wood often contains soluble salts and iron sulfides, which pose a threat to its stability. Therefore, desalination treatment must be carried out during protection. In this study, deionized water and ethylene diamine tetraacetic acid disodium salt (EDTA-2Na) solution were used to extract soluble salts and iron sulfides from the 511 wood components of the “Huaguangjiao I” shipwreck. The extraction lasted for 1120 days, during which extraction progress was monitored by measuring the electrical conductivity and iron content of the soaking solution. The results indicated that the extraction experiment reached its endpoint when the conductivity of the soaking solution was maintained at 80~100 μs/cm and the iron content was maintained at 8~15 mg/L. More than 143.35 kg of iron were extracted from the wood of the “Huaguangjiao I” shipwreck. After extraction, the content of soluble salt ions in the wood were less than 5 μg/g, with an iron content below 5%. The wood has returned to its original color and with a certain degree of degradation. “Huaguangjiao I” was the first large-scale marine shipwreck to complete the desalination treatment of all wooden components. This study provides guidance for the desalination treatment of large-scale wooden shipwrecks.

Enhanced osteogenicity of the demineralized bone-dermal matrix composite by the optimal partial demineralization for sustained release of bioactive molecules.

Allogenic demineralized bone matrix (DBM), processed to expose bioactive proteins imbedded by calcium salts, is widely used for bone repair and regeneration as an alternative to the autologous bone graft. However, demineralized bone matrices from tissue banks vary significantly in residual calcium content and osteogenicity for clinical bone regeneration. The present study produced DBM with various residual calcium contents by partial demineralization using ethylenediaminetetraacetic acid disodium (EDTA) and hydrochloric acid. Compositional analysis reveals that, as the percent weight loss of bone materials increases from 0% to 74.9% during demineralization, the residual calcium content of DBM decreases from 24.8% to 0.2% and collagen content increases from 29.7% to 92.6%. Calorimetrical analysis and Fourier transform infrared (FTIR) analysis demonstrated that demineralization to the residual calcium content of <4% enables the complete exposure and/or release of bone collagen fibers and other bioactive molecules. In order to evaluate the relationship between the extent of demineralization and the osteogenicity of DBM, DBM particles were fabricated with the aid of acellular dermal matrix (ADM) microfibers to form flexible foam-like DBM/ADM composites. Proteomic analysis identified various type collagens and bone formation-related bioactive molecules in both ADM and DBM. Using the rat bilateral Φ = 5 mm calvarium defect repair model, the study had shown that the DBM/ADM composite with ~20% DBM residual calcium (e.g., ~40% calcium being removed) maximized the osteogenicity for bone defect repair after 4 and 8 weeks. DBM with ~40% calcium removal had the maximal osteogenicity presumably through the sustained release of bioactive molecules during the process of bone regeneration.

Evaluate the Depression of High-Concentration Pyrite in Copper Flotation by High-Chromium Grinding Media

ABSTRACT The copper (Cu) concentrators have to process high-pyrite-content ores due to rapid depletion of high-grade ores and a high demand for Cu by clean energy technologies. However, depressing high-concentration pyrite in copper flotation is challenging presently. For the first time, this study evaluated 30 wt% Cr steel, a type of high-chromium (HiCr) steel grinding media, which can effectively produce a high Cu concentrate grade in processing low-concentration pyrite ores, in treating 25% pyrite in a Cu feed at 1.7% Cu in comparison with treating 5% pyrite in a Cu feed at the same Cu grade. Flotation tests showed decreased Cu grade and Cu recovery as pyrite feed grade increased from 5% to 25%, which was attributed to the changed galvanic interaction between grinding media and sulfide minerals, supported by ethylene diamine-tetra acetic acid disodium extraction, pulp chemistry measurements, and electrochemical studies. As pyrite feed grade increased from 5% to 25%, the anodic role of 30 wt% Cr steel did not change, but the anodic role of chalcopyrite and the cathodic role of pyrite were enhanced, promoting chalcopyrite oxidation while retarding pyrite oxidation, both of which facilitated copper activation on pyrite and subsequent pyrite flotation. This study also compared 30 wt% Cr steel and traditional forged steel in depressing 25% pyrite in the feed, and forged steel poorly depressed pyrite due to a strong anodic role of forged steel and a strong cathodic role of pyrite during the galvanic interaction leading to strong copper activation on pyrite. This study points to a direction how to depress high-concentration pyrite in copper flotation.

A robust & weak-nucleophilicity electrocatalyst with an inert response for chlorine ion oxidation in large-current seawater electrolysis

Seawater splitting into hydrogen, a promising technology, is seriously limited by the durability and tolerance of electrocatalysts for chlorine ions in seawater at large current densities due to chloride oxidation and corrosion. Here, we present a robust and weak-nucleophilicity nickel–iron hydroxide electrocatalyst with excellent selectivity for oxygen evolution and an inert response for chlorine ion oxidation which are key and highly desired for efficient seawater electrolysis. Such a weak-nucleophilicity electrocatalyst can well match with strong-nucleophilicity OH− compared with the weak-nucleophilicity Cl−, resultantly, the oxidation of OH− in electrolyte can be more easily achieved relative to chlorine ion oxidation, confirmed by ethylenediaminetetraacetic acid disodium probing test. Further, no strongly corrosive hypochlorite is produced when the operating voltage reaches about 2.1 V vs. RHE, a potential that is far beyond the thermodynamic potential of chlorine ion oxidation. This concept and approach to reasonably designing weak-nucleophilicity electrocatalysts that can greatly avoid chlorine ion oxidation under alkaline seawater environments can push forward the seawater electrolysis technology and also accelerate the development of green hydrogen technique.

“EDTA•2Na-Mn+” based-signal regulation strategy for the construction of vigorous and progressive detection platforms with various signals

The “ethylenediamine tetraacetic acid disodium salt-metal” (“EDTA•2Na-Mn+”) based-signal regulation strategy has been successfully developed for the construction of vigorous and progressive immunoassays with various signals, including 1) EDTA•2Na-Fe3+@aptamer/gold nanorods (Ea-Fe3+/AuNRs) with photothermal signal; 2) silica nanoparticles (SiO2 NPs) @EDTA•2Na-Au3+@aptamer/gold nanoparticles (Sea-Au3+/AuNPs) with colorimetric signal; 3) SiO2 NPs@EDTA•2Na-Cd2+@aptamer-cDNA/gold nanoclusters (Seac-Cd2+/AuNCs) with fluorescence signal. Concretely, EDTA•2Na chelates Fe3+, Au3+, and Cd2+ fiercely to selectively regulate the metallization of AuNRs, growth of AuNPs, and synthesis of AuNCs. Using Aflatoxin B1 as a model target, these assays could achieve limits of detection at 0.15 pg/mL, 0.19 pg/mL, and 0.2 fg/mL, respectively. The relative standard deviation of 2.17 % indicates good consistency for food samples detection. Compared with conventional ELISA, these high-performance enzyme-free “EDTA•2Na-Mn+” platforms exhibit the superiors of low cost and enhanced sensitivity, thereby expanding the building of biosensors that eliminate the use of enzymes. Importantly, these platforms endow multiple signals that can realize the mutually corroborate with noninterference for one target detection. The diversity of signals endows the flexible selection of those platforms for food samples detection with different colors and matrices.

Effect of nisin, EDTA, and abuse temperature on the growth of Salmonella Typhimurium in liquid whole egg during refrigerated storage

Salmonella spp. can be present in pasteurized liquid egg products because of its heat resistance or post-processing contamination, thereby representing a food safety risk. The effect of 1000 IU nisin/ml plus 20 mM disodium ethylenediaminetetraacetic acid (EDTA), two refrigerated temperatures (7 °C and 10 °C), and two inoculation levels (103 and 105 cfu/ml) were studied in the growth of S. Typhimurium in pasteurized liquid whole egg (LWE). Two mathematical models were used to fit the microbial curves. Physicochemical characteristics of LWE, such as pH and color, were assessed for 31 days at the two storage temperatures, and no significant changes (p < 0.05) were observed for most of the samples. Results showed the significant impact of temperature on microbial growth. Samples kept at 7 °C showed the decay of microbial cells during storage; meanwhile, the effect at 10 °C was shown as fast growth. The combination of nisin plus EDTA and 7 °C accelerated the decay of microbial cells during the storage showing a synergistic effect. The Weibull model described the decline of cells during the shelf-life. Meanwhile, the logistic model fitted the growth of Salmonella in LWE at 10 °C. Adding these additives to LWE, combined with the correct temperature during pasteurization and adequate conditions during the cold chain, can minimize the food safety risk related to Salmonella.

Impact of Mn2+ in bisphenol A degradation by chelating agents-assisted manganese dioxide: Mechanism understanding and efficiency evaluation

Manganese dioxide (MnO2) is popular in eliminating organic pollutants in water. The application of chelating agents to enhance the reactivity of MnO2 has been previously reported. Much attention has been taken to increase the amount of Mn(III) species in the manganese oxide/ligands system to achieve a higher degradation. However, the role of Mn2+ is rarely studied. In this study, the efficiency and mechanism of bisphenol A (BPA) degradation by pyrophosphate (PP)-assisted MnO2 in the presence of Mn2+ was investigated. The results show that 25 μM of BPA can be completely removed by the MnO2/PP/Mn2+ system in 90 min. Increasing PP and Mn2+ concentrations effectively improved the degradation of BPA. The primary reactive species for the degradation of BPA was determined to be the Mn(III)-PP complex. Moreover, Mn2+ were verified to play the bridging, reductive, and catalytic roles to enhance the degradation of BPA. Furthermore, the substituted ligands such as nitrilotriacetic acid (NTA) and ethylenediaminetetraacetic acid disodium salt hydrate (EDTA) were verified to exhibit higher activity than citrate on MnO2 activation in the presence of Mn2+. The adaptability of the proposed system was evaluated in various conditions such as the presence of metal cations or inorganic ions and wide solution pH range. In addition, the performance of MnO2/PP/Mn2+ system on BPA removal in the sewage treatment plant outlet water was evaluated as well. These findings highlight the positive role of Mn2+ in the system of MnO2/ligands and provide a practical reference for the application of ligands-assisted manganese oxides in wastewater treatment.

Crab-claw inspired high performance and flame-retardant magnesium oxychloride cement based adhesive reinforced by 4-arms EDTA and tartaric acid for wood industry

The high CO2 emissions and instability of silicate cement binders during production and use have encouraged the development of low-carbon materials. In this study, an environmentally friendly and flame-retardant building material was produced from magnesium oxychloride cement (MOC) and wood. In practice, the considerable microcracking that forms during the hardening process makes MOC materials very sensitive to water, which limits their further use. Inspired by the predation of crabs, a simple and effective method was proposed to obtain better water resistance and mechanical strength of MOC composite by co-modifying with ethylenediaminetetraacetic acid (EDTA) or disodium ethylenediaminetetraacetic acid (EDTA-Na) in conjunction with tartaric acid. The four –COOH of EDTA and EDTA-Na coordinated well with the 5-phase structure and tightly aggregated the 5-phase crystals, effectively reducing the formation of microcracks. The synergistic effect between EDTA/EDTA-Na and tartaric acid prevented the disruption of 5-phase crystal structures by water molecules, thus improving the water resistance of the MOC composite. The softening coefficients of the MOC composite modified by EDTA and EDTA-Na in cooperation with tartaric acid after soaking for seven days were 0.97 and 0.98, respectively, which is significantly higher than that of the MOC composite modified by tartaric acid alone (0.54). At the same time, the co-modified MOC composite can be utilised as an inorganic adhesive for plywood, and the wet strength of plywood modified with EDTA in cooperation with tartaric acid being 25% higher than that of the unmodified MOC composite. In addition, the resulting composites showed great potential for application in low-carbon building materials, which can help alleviate the environmental impact of construction industries.

A Novel Ion Species- and Ion Concentration-Dependent Anti-Counterfeiting Based on Ratiometric Fluorescence Sensing of CDs@MOF-Nanofibrous Films.

Traditional fluorescent anti-counterfeiting labels based on "on-off" fluorescence can be easily cloned. It is important to explore advanced anti-counterfeiting fluorescent labels with high-level security. Here, a pioneering ion species- and ion concentration-dependent anti-counterfeiting technique is developed. By successive loading Cu2+ -sensitive yellow emitted carbon dots (Y-CDs) and Cu2+ non-sensitive blue emitted carbon dots (B-CDs) into metal-organic frameworks (MOFs) and followed by electrospinning, the B&Y-CDs@MOF-nanofibrous films are prepared. The results show that the use of MOF not only avoids the fluorescence quenching of CDs but also improves the fluorescence stability. The fluorescence Cu2+ -sensitivity of the CDs@MOF-nanofibrous films can be regulated by polymer coating or lamination. The fluorescent label consisting of different Cu2+ -sensitivity films will show Cu2+ concentration-dependent decryption information. Only at a specific ion species and concentration (Cu2+ solution of 40-90µm), the true information can be read out. Less or more concentration (<40 or >90µm) will lead to false information. The identification of the real information depends on both the species and the concentration. After Cu2+ treatment, the fluorescence of the label can be recovered by ethylenediaminetetraacetic acid disodium (EDTA-2Na) for further recycling. This work will open up a new door for designing high-level fluorescent anti-counterfeiting labels.