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Context: In vitro embryo production in pigs is an important tool for advancing biomedical research. Intracytoplasmic sperm injection (ICSI) circumvents the polyspermy problems associated with conventional IVF in porcine. However, the suboptimal efficiency for ICSI in pigs requires new strategies to increase blastocyst formation rates. Aim: To investigate novel methods for assisted activation using the zinc chelator 1,10-phenanthroline (PHEN), and to improve embryo developmental competence and quality of ICSI porcine blastocyst. Methods: ICSI embryos were treated with PHEN after or before sperm injection, recording pronuclear formation, blastocyst rate and the expression of SMARCA4, OCT4, SOX2 and CDX2. Key results: Neither electrical nor PHEN significantly improves pronuclear formation rates before or after ICSI. Following in vitro culture to the blastocyst stage, no significant differences were observed in developmental rates among the groups. Moreover, the use of PHEN did not alter the total cell number or the expression of OCT4, SOX2 and CDX2 in pig ICSI blastocysts. Conclusions: Assisted oocyte activation with PHEN does not affect the preimplantation development of ICSI-derived pig embryos. Implications: These results hold significance in refining and advancing the application of assisted oocyte activation techniques. They offer insights into addressing fertility issues and propelling advancements in human and animal reproductive medicine. Improving pig embryo development holds great promise for agriculture and biomedical research. This study investigated the use of a zinc chelator, 110-phenanthroline, to enhance assisted oocyte activation in pigs following intracytoplasmic sperm injection. While no differences in embryo development or quality were found, this indicates that zinc chelation is a potentially safe method for inducing oocyte activation, providing a foundation for future advancements in human and animal assisted reproductive research. Image generated by ChatGPT-4 (OpenAI, 2024). [ABSTRACT FROM AUTHOR]

AAZTA (6-amino-6-methylperhydro-1,4-diazepinetetraacetic acid) is a mesocyclic chelating agent forming stable complexes with several metal ions. Over the past 20 years since its inception, AAZTA and its bifunctional derivatives have gained a growing role in several applications ranging from MRI contrast agents to diagnostics and nuclear medicine. The recent market restrictions applied to nitroethane preclude the easy preparation of AAZTA, prompting the search for a suitable alternative. In this work, we report the synthesis of two structural analogs (AAZTA-Bn and AAZTA-Et) from commercially available chemicals and the thermodynamic and kinetic study of their complexing ability towards selected metal ions. A comparison of the complexing properties of AAZTA-Bn and AAZTA-Et with the former AAZTA allows us to identify the possible heir of this efficient chelating agent. [ABSTRACT FROM AUTHOR]

The rapid design of advanced materials depends on synthesis parameters and design. A wide range of materials can be synthesized using precursor reactions based on chelated gel and organic polymeric gel pathways. The desire to develop high-performance lithium-ion rechargeable batteries has motivated decades of research on the synthesis of battery active material particles with precise control of composition, phase-purity, and morphology. Among the most common methods reported in the literature to prepare precursors for lithium-ion battery active materials, sol-gel is characterized by simplicity, homogeneous mixing, and tuning of the particle shape. The chelate gel and organic polymeric gel precursor-based sol-gel method is efficient to promote desirable reaction conditions. Both precursor routes are commonly used to synthesize lithium-ion battery cathode active materials from raw materials such as inorganic salts in aqueous solutions or organic solvents. The purpose of this review is to discuss synthesis procedure and summarize the progress that has been made in producing crystalline particles of tunable and complex morphologies by sol-gel synthesis that can be used as active materials for lithium-ion batteries. [ABSTRACT FROM AUTHOR]

Objective The drilling wastewater in a block of Changqing Oilfield is large in volume, complex in composition, and high in Ca2+ and other multivalent ions, which makes it challenging to meet the requirements of fracking fluid blending performance after conventional treatment. Methods Based on the above difficult process characteristics, a new type of calcium removal process was proposed by modifying chitosan with multifunctional groups to chelate Ca2+, and its effect on calcium removal, calcium removal mechanism, applicable conditions (temperature, pH), environmental impact (mud production) and back-mixing performance were evaluated. Results The results showed that chitosan with a high degree of deacetylation was used as raw material, potassium persulfate was used as initiator to graft acrylic acid, and chitosan: potassium persulfate: acrylic acid=1.0:1.2:25.0 was reacted under the conditions of temperature of 70 ℃ for 2 h to produce highly water-soluble multifunctional chelating agent, and the Ca2+ could be chelated and removed to less than 500 mg/L by using 600 mg/L SZ-1. SZ-1 could be applied under the conditions of 10-40 ℃, pH=6-14, with low sludge production (0.016 g/L) and suitable viscosity of base fluid (30.9~31.2 mPa?s), which satisfied the requirements of base fluid viscosity range (10-40 mPa?s) in SY/T 7627—2021 Technical requirements of water-based fracturing fluid. Conclusion It is expected to provide a new solution for the treatment of drilling wastewater with high calcium content in oil and gas fields, with its green and clean color, excellent performance, and simple preparation. [ABSTRACT FROM AUTHOR]

Phytic acid (inositol hexaphosphate/IP6) is a versatile chemical that is abundant in nature and is required for a variety of biological processes. It is harnessed in a wide range of fields, including drug discovery, daily supplies, chemical industries, medicine, and dentistry. IP6 is becoming increasingly popular in dentistry, with promising results. Several properties, such as cariostatic ability, beneficial impact on enamel disintegration, and anti-plaque, anti-tartar, and dental adhesive-forming properties, have been investigated thus far. Due to many constraints in the literature, there was a point in time when IP6 received less attention, which impacted knowledge in this field. Nevertheless, the positive outcomes of the flourishing of IP6 have recently been reconsidered from a number of papers that have improved our understanding of its modes of action in the aforementioned applications. The role of phytic acid in refining the properties and manoeuvring of dental resources is being investigated in novel endeavors in treating diseases of pulp and tissues supporting tooth structure, but to show its novel therapeutic potential, more precisely calibrated clinical trials are needed. This review examines and discusses the various uses proposed in the literature, as well as the applications of IP6 in dentistry. [ABSTRACT FROM AUTHOR]

The need to combine various metals in light-weight constructions requires the development of coatings that prevent galvanic corrosion. Layered double hydroxides (LDHs) can be an example of such coatings, which were previously successfully obtained in situ on individual materials. In addition, the possibility of LDH growth (including LDH growth in the presence of chelating agents) on the surface of plasma electrolytic oxidation (PEO)-coated metals was previously shown. This PEO ​+ ​LDH combination could improve both corrosion and mechanical characteristics of the system. The possibility of LDHs formation in situ on the surface of PEO-coated friction stir welded (FSW) magnesium-aluminum materials (AZ31/AA5754 system was selected as a model one) was demonstrated in the presence of 1,3-diamino-2-hydroxypropane-N,N,N’,N’-tetraacetic acid (DHPTA) as a chelating agent, which was selected based on analysis of respective metal-ligand compounds stability. LDHs growth was achieved under ambient pressure without addition of carbonates in the electrolyte. The effectiveness of the resulting coating is shown both for corrosion resistance and hardness.

Phytic acid (inositol hexaphosphate/IP6) is a versatile chemical that is abundant in nature and is required for a variety of biological processes. It is harnessed in a wide range of fields, including drug discovery, daily supplies, chemical industries, medicine, and dentistry. IP6 is becoming increasingly popular in dentistry, with promising results. Several properties, such as cariostatic ability, beneficial impact on enamel disintegration, and anti-plaque, anti-tartar, and dental adhesive-forming properties, have been investigated thus far. Due to many constraints in the literature, there was a point in time when IP6 received less attention, which impacted knowledge in this field. Nevertheless, the positive outcomes of the flourishing of IP6 have recently been reconsidered from a number of papers that have improved our understanding of its modes of action in the aforementioned applications. The role of phytic acid in refining the properties and manoeuvring of dental resources is being investigated in novel endeavors in treating diseases of pulp and tissues supporting tooth structure, but to show its novel therapeutic potential, more precisely calibrated clinical trials are needed. This review examines and discusses the various uses proposed in the literature, as well as the applications of IP6 in dentistry.

The prevalent use of nanoparticles has adverse negative effects on biosystems. Subsequently, this study aimed to use Caelatura nilotica to assess the ecotoxicity of TiO2 NPs and how Dimercaptosuccinic acid (DMSA) improves these effects. Two concentrations of TiO2 NPs (25 and 150 µg/L) were used for 28 days. TiO2 NPs bioaccumulation, gonadal weight, gonado‐somatic index, and histopathological alterations of gonads were determined. The tissues' accumulation of TiO2 NPs was concentration‐time‐dependent: it was 78.5 ± 28.93 μg/g dry weight in the exposed clams to 150 µg/L TiO2 NPs after 4 weeks of exposure. The gonadal weight and gonado‐somatic index significantly decreased of the exposed group to 150 µg/L TiO2 NPs over the experimental period that they ended with values (1.01 ± 0.57 gm, 19.15 ± 7.75%, respectively). There are some histological alterations in the gonads of C. nilotica such as necrosis, deteriorated connective tissue, increased fibrous tissue, a reduced presence of mature sperms and mature ova, and irregular shapes of testicular/ovarian follicles. When using Dimercaptosuccinic acid (DMSA), this led to a reduction in accumulation of TiO2 NPs by the end of the experiment. So, C. nilotica is a promising model to reflect the adverse nano‐toxics. DMSA emerges as a potentially valuable chelating agent that abolishes the negative effects of these nanoparticles. Highlights: Titanium oxide nanoparticles affect the histology and biometry of Caelatura nilotica gonads.C. nilotica can accumulate even minute quantities, of TiO2 NPs and bulk form.C. nilotica is a promising model to reflect the adverse effects of nanomaterials.Dimercaptosuccinic acid (DMSA) can abolish the negative effects of nanoparticles.DMSA can protect C. nilotica clams in nanoparticles polluted ecosystems. [ABSTRACT FROM AUTHOR]

The use of diethylenetriaminepentaacetic acid (DTPA) chelating agent has shown promising results for enhanced oil recovery (EOR) in prior research. Several mechanisms, mainly resulting from rock-fluid interaction, have been proposed for chelating agent flooding; however, little attention has been paid to fluid-fluid interaction thus far. The assessment of these mechanisms has primarily relied on macroscopic techniques such as core flooding. This paper aims to investigate the injection of DTPA brine and its dominant mechanisms at the pore scale using a clay-coated micromodel. The micromodel tests were performed under oil-wet and water-wet states. For a more precise examination of fluid/fluid interactions, the dynamic interfacial tension (IFT) and Zeta potential were measured. It was observed that the injection of DTPA brine in water-wet state changed the saturation distribution and increased oil recovery. Based on visual inspections, this change in saturation distribution could potentially be linked to the formation of micro-dispersions and viscoelastic interfacial phenomena. Micro-dispersions facilitate flow to unswept areas, and viscoelastic interface formation reshapes the interface between oil and brine, causing disconnected oil droplets to coalesce and thus increase recovery. Under the oil-wet state, the micro-dispersion formation and wettability alteration can be the dominant mechanisms, and the amount of recovered oil was higher than that observed in the water-wet state. Furthermore, Zeta potential measurements at the interface between brine and oil showed a more negative value for DTPA brine, which is effective in wettability alteration and micro-dispersions stability. The results indicate that IFT reduction was not significant enough to be considered the dominant mechanism, although it assists in DTPA brine penetration into the crude oil and subsequent micro-dispersion formation.

New compounds series of [M(TMP)(en)]X·nH2O and [M(TMP)(PD)]X·nH2O, where M = Ni2+, Cu2+, Zr4+, Ag+, Cd2+, TMP = trimethoprim, en = ethylenediamine, PD = o-phenylene and X= Cl− or NO3−, were prepared. The compounds were characterized using techniques including melting points, conductance, elemental analysis, FTIR, NMR, and mass spectroscopy. FTIR spectra indicated TMP acted like a bi-dentate ligand, combining via the nitrogen atoms of azomethine and pyrimidine amino groups. Diamine ligands (en or o-PD) are coordinated via two nitrogen atoms. Prepared compounds showed monomeric behavior and adopted a 6-coordinate octahedral geometry based on magnetic susceptibility and UV spectra. Conductivity measurements revealed Zr(IV) compounds were 1:2 conductive, while Ag+ and Cd2+ were 1:1 conductive; Ni2+ and Cu2+ compounds were non-conductive. Antibacterial tests on compounds and ligands against Bacillus subtilis and Staphylococcus aureus demonstrated broad-spectrum antibacterial activity. The mixed metal compounds revealed an observable tendency of antibacterial activity in the order Zr > Cd = Ag > Cu, making Zr(IV) compounds the most biologically active among them against S. aureus (Gram-positive) while the same compounds showed less antibacterial activity against B. subtilis (Gram-negative) than the free ligand.

Copyright of Turkiye Klinikleri Journal of Dental Sciences is the property of Turkiye Klinikleri and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

In the field of stone conservation, the removal of iron stains is one of the most challenging issues due to the stability and low solubility of the ferrous species. In the present paper, three different chitosan-based hydrogels added with acetic, oxalic or citric acids are applied on different lithotypes, i.e., granite, travertine and marble, widely diffused in monumental heritages, and artificially stained by deposition of a rust dispersion. The reducing power of carboxylic acids is combined with the good chelating properties of chitosan to effectively remove rust from stone surfaces. As evidenced by colorimetry on three samples of each lithotype and confirmed by 1H-NMR relaxometry and SEM/EDS analyses, the chitosan-oxalic acid hydrogel shows the best performance and a single application of 24 h is enough to get a good restoration of the stone original features. Lastly, the chitosan-oxalic acid hydrogel performs well when a rusted iron grid is placed directly on the lithic surfaces to simulate a more realistic pollution. Current work in progress is devoted to finding better formulations for marble, which is the most challenging to clean or, with a different approach, to developing protective agents to prevent rust deposition. [ABSTRACT FROM AUTHOR]

Heavy metals in flue gas desulfurization (FGD) gypsum from coal-fired power plants are at risk of releaching during the processes of stockpiling and resource utilization. In this study, the effects of organosulfur chelators dithiocarbamate (DTC) and trisodium trithiocyanate-15 (TMT-15) on the solidification characteristics of heavy metals in desulphurized gypsum under different mass fractions, pH values, water contents and reaction times were investigated. The chemical composition and morphology were analyzed by inductively coupled plasma atomic emission spectrometer (ICP-AES) and scanning electron microscope (SEM). The experiments showed that both DTC and TMT-15 were effective at stabilizing the heavy metals in the FGD gypsum, with more than a 50% curing effect for all the heavy metals except Pb. DTC showed a better stabilization for Pb, Hg, Cu, Zn, and Cr, and TMT-15 showed a better curing effect for Cd. The solidified gypsum had good heavy metal stability in low-water-content environments. Increasing the mass fraction, reaction time, and pH decreased the heavy metal leaching, and the mass fraction had the greatest effect on the total heavy metal leaching concentration, followed by the reaction time and pH value. [ABSTRACT FROM AUTHOR]

Protein–protein and protein–mineral interactions can result in defects, such as sedimentation and age gelation, during the storage of high-protein beverages. It is well known that age gelation can be delayed by adding cyclic polyphosphates such as sodium hexametaphosphate (SHMP). This study aims to assess the influence of different phosphate chain lengths of SHMP on the physicochemical properties of high-protein dispersions. The effect of adding different SHMP concentrations at 0%, 0.15%, and 0.25% (w/w) before and after heating of 6%, 8%, and 10% (w/w) milk protein concentrate dispersions was studied. The phosphate chain lengths of SHMPs used in this study were 16.47, 13.31, and 9.88, and they were classified as long-, medium-, and short-chain SHMPs, respectively. Apparent viscosity, particle size, heat coagulation time (HCT), color, and turbidity were evaluated. It was observed that the addition of SHMP (0.15% and 0.25%) increased the apparent viscosity of MPC dispersions. However, the chain length and the concentration of the added SHMP had no significant (p > 0.05) effect on the apparent viscosity after heating the dispersions. The HCT of a dispersion containing 6%, 8%, and 10% protein with no SHMP added was 15.28, 15.61, and 11.35 min, respectively. The addition of SHMP at both levels (0.15% and 0.25%) significantly increased the HCT. Protein dispersions (6%, 8%, and 10%) containing 0.25% short-chain SHMP had the highest HCT at 19.29, 19.61, and 16.09 min, respectively. Therefore, the chain length and concentration of added SHMP significantly affected the HCT of unheated protein dispersion (p < 0.05). [ABSTRACT FROM AUTHOR]

While low salinity water (LSW) holds promise for improving oil recovery, its implementation is comparatively costly due to the substantial volumes of fresh water required to dilute seawater (SW). Additionally, concerns arise regarding potential issues related to LSW, including fines migration in sandstone reservoirs and scale formation in carbonate reservoirs. Chelating agents can be introduced into undiluted SW to bind with metal ions, thereby lowering its salinity. This approach mimics the behavior of LSW injection while overcoming associated challenges. This study involves measuring oil/injected solution interfacial tension (IFT), evaluating sandstone surface wettability alteration, along with conducting different sand pack flooding scenarios using Ethylenediaminetetraacetic acid (EDTA) chelating agent. The aim was to comprehend the EDTA oil recovery mechanisms and determine the optimal concentration of EDTA that minimizes chemical consumption while maximizing oil recovery. The findings indicated that incorporating 5 wt% EDTA into SW significantly reduced IFT from 29.52 mN/m to 4.75 mN/m, making the oil nearly miscible in the solution. Moreover, wettability tests confirmed that a minimum EDTA concentration of 5 wt% is required to shift wettability from oil-wet to strongly water-wet conditions. Sand pack flooding experiments, on the other hand, further demonstrated that this optimized fluid system can potentially recover an additional 16.1 % of oil following SW flooding. Finally, inductively coupled plasma (ICP) analysis revealed a notable increase in metal ion concentration during EDTA flooding, indicating enhanced leaching of metals from the sandstone surface and improved wettability characteristics.

Metal oxide catalysts (MOCs) for the growth of carbon nanotubes with the general composition Fe2Co/CaCO3 were synthesized by the polymerized complex precursor (PCP) method using chelating agents. It has been established that metal oxide catalysts synthesized by the method of polymerized complex precursors are an order of magnitude more effective than MOCs synthesized by the sol-gel technology. The productivity of MOCs obtained using two ligands is significantly higher than the efficiency of monoligand samples. As a result of the study, it was found that the use, in addition to carbohydrates, of a wide range of chelating agents of various natures (polyalcohols, hydroxy acids, amino acids, etc.) in the synthesis of metal oxide catalysts for the growth of CNTs by the method of polymerized complex precursors is advisable and makes it possible to affect the stage of preorganization of the structure of MOCs precursor, specific productivity of metal oxide catalysts as well as qualitative composition of carbon products. [ABSTRACT FROM AUTHOR]

In order to reduce the energy consumption of the reaction, the magnesium alloy samples were immersed directly into three conversion solutions and reacted for 9 hours at 60 ℃ and pH=12.0 used the chelating agent-assisted method by adding three chelating agents, ethylenediaminetetraacetic acid tetrasodium (EDTA-4Na), sodium citrate (SC) and potassium sodium tartrate (PST) to aluminum nitrate (Al(NO3)3) solution, and Mg-Al layered double hydroxides (LDHs) films doped with different chelating agents can be prepared on the surface of magnesium alloys. The microstructure, phase composition, and corrosion resistance of each LDHs film were analyzed by SEM, XRD, FT-IR, etc. The results show that the chelating agent-assisted method can successfully prepare LDHs films with typical layered structure on the surface of magnesium alloys under normal pressure and 60 ℃ environment; and three kinds of Mg-Al LDHs films obtained can effectively improve the corrosion resistance of magnesium alloys. Then, by comparing the structural properties of three different LDHs film layers, it is found that the Mg-Al-PST LDHs film prepared by adding PST has the highest density and the largest thickness, reaching up to 1.4 μm. The improvement effect of three coatings on the corrosion resistance of magnesium alloys is as follows: Mg-Al-PST LDHs > Mg-Al-SC LDHs > Mg-Al-EDTA LDHs; The magnesium alloy covered with the Mg-Al-PST LDHs film compared to the blank magnesium alloy, the corrosion current density decreases by about two orders of magnitude, and the total corrosion resistance increases by about one order of magnitude. And based on the analysis of the structure and properties of the obtained LDHs films, it can be seen that the chelating agent-assisted method can prepare Mg-Al LDHs films with better corrosion resistance in-situ on the surface of magnesium alloys under the lower energy consumption condition. The reason may be that the carboxyl group in the chelating agent can accelerate the deposition of Al3+ on the magnesium substrate and promote the substitution of some Mg2+ in Mg (OH)2 by Al3+ to form LDHs.

Polysaccharides are functional foods or drugs that can be used to alleviate heavy metal poisoning by cadmium, lead, mercury, and arsenic. Industries generate substantial quantities of toxic heavy metal wastes, such as wastewater discharges, paints, electronic waste, batteries, pigments, and plastics, into the environment that pose a risk to human health. Therefore, it is imperative to eliminate accumulated heavy metal ions from the body and the environment. Heavy metal toxicity can lead to decreased energy levels and impair the functioning of vital organs, such as the brain, lungs, kidneys, liver, and blood. Prolonged exposure can result in progressive physical, muscular, and neurological degeneration that resembles conditions such as multiple sclerosis, Parkinson's disease, Alzheimer's disease, and muscular dystrophy. Polysaccharides operate through mechanisms such as chelation, antioxidant defense, immunomodulation, and tissue repair. Polysaccharides involved in heavy metal removal include methionine and cysteine, together with N-acetylcysteine, an acetylated form of cysteine, S-adenosylmethionine, a metabolite of methionine, α-lipoic acid, and the tripeptide glutathione (GSH). These compounds effectively bind with harmful heavy metals to create a stable complex and defend biological targets from metal ions, thus decreasing their harmful effects and causing them to be excreted from the body. This review also highlights the importance of polysaccharides' ability to mitigate oxidative stress, enhance immune responses, and support tissue repair processes. Polysaccharides are ubiquitous in nature and take part in diverse processes, making them potential natural therapies for heavy metal-related diseases. This review discusses the effectiveness of natural polysaccharides and the mechanisms that allow them to bind with heavy metals to alleviate their effects from the body and the environment. Polysaccharides have inherent features that enable them to function as pharmacological agents and regulate the immune response. [ABSTRACT FROM AUTHOR]

Copyright of Journal of Materials Engineering / Cailiao Gongcheng is the property of Journal of Materials Engineering Editorial Office and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Greenly synthesized nanoparticles have garnered attention due to their low environmental footprint, but impurities limit their applications. A novel semi-organic method for synthesizing silver nanoparticles (AgNPs) using bio-based chelating fuels (Beta vulgaris subsp., Spinacia oleracea, and Ipomoea batatas) reduces the undesirable impurities. The study also showcases the impact of bio-based chelating fuel on various characteristics of AgNPs in comparison to synthetic chelating fuel. The antimicrobial efficacy of the synthesized AgNPs in conjunction with honey was also assessed against E. coli. The XRD analysis showed cubic structure of AgNPs. The FESEM and TEM analysis showed that the well-connected spherical-shaped AgNPs (∼3–120 nm diameter) while EDS confirmed the presence of Ag in all samples. The TEM analysis also revealed layers of carbonates in AgNPs synthesized using bio-based chelating fuels. XPS investigation confirmed the absence of any prominent impurities in prepared samples and AgNPs have not experienced oxidation on their surface. However, notable surface charging effects due to the uneven conductivity of the particles were observed. The broth dilution method showed that all mixtures containing AgNPs in combination with honey exhibited a significant bacterial growth reduction over a period of 120 h. The highest growth reduction of ∼75 % is obtained for the mixture having AgNPs (Ipomoea batatas) while the least growth reduction of ∼51 % is obtained for the mixture having AgNPs (Beta vulgaris subsp.). The findings affirm that AgNPs can be successfully synthesized using bio-based chelating fuels with negligible ecological consequences and devoid of contaminants. Moreover, the synthesized AgNPs can be employed in conjunction with honey for antibacterial purposes.

The rapid design of advanced materials depends on synthesis parameters and design. A wide range of materials can be synthesized using precursor reactions based on chelated gel and organic polymeric gel pathways. The desire to develop high-performance lithium-ion rechargeable batteries has motivated decades of research on the synthesis of battery active material particles with precise control of composition, phase-purity, and morphology. Among the most common methods reported in the literature to prepare precursors for lithium-ion battery active materials, sol-gel is characterized by simplicity, homogeneous mixing, and tuning of the particle shape. The chelate gel and organic polymeric gel precursor-based sol-gel method is efficient to promote desirable reaction conditions. Both precursor routes are commonly used to synthesize lithium-ion battery cathode active materials from raw materials such as inorganic salts in aqueous solutions or organic solvents. The purpose of this review is to discuss synthesis procedure and summarize the progress that has been made in producing crystalline particles of tunable and complex morphologies by sol-gel synthesis that can be used as active materials for lithium-ion batteries.

AAZTA (6-amino-6-methylperhydro-1,4-diazepinetetraacetic acid) is a mesocyclic chelating agent forming stable complexes with several metal ions. Over the past 20 years since its inception, AAZTA and its bifunctional derivatives have gained a growing role in several applications ranging from MRI contrast agents to diagnostics and nuclear medicine. The recent market restrictions applied to nitroethane preclude the easy preparation of AAZTA, prompting the search for a suitable alternative. In this work, we report the synthesis of two structural analogs (AAZTA-Bn and AAZTA-Et) from commercially available chemicals and the thermodynamic and kinetic study of their complexing ability towards selected metal ions. A comparison of the complexing properties of AAZTA-Bn and AAZTA-Et with the former AAZTA allows us to identify the possible heir of this efficient chelating agent.

Chelating agents are commonly employed in microelectronic processes to prevent metal ion contamination. The ligand fragments of a chelating agent largely determine its binding strength to metal ions. Identification of ligands with suitable characteristics will facilitate the design of chelating agents to enhance the capture and removal of metal ions from the substrate in microelectronic processes. This study employed quantum chemical calculations to simulate the binding process between eleven ligands and the hydrated forms of Ni2+, Cu2+, Al3+, and Fe3+ ions. The binding strength between the metal ions and ligands was quantified using binding energy and binding enthalpy. Additionally, we explored the binding interaction mechanisms and explained the differences in binding abilities of the eleven ligands using frontier molecular orbitals, nucleophilic indexes, electrostatic potentials, and energy decomposition calculations based on molecular force fields. Based on our computational results, promising chelating agent structures are proposed, aiming to guide the design of new chelating agents to address metal ion contamination issues in integrated circuit processes. [ABSTRACT FROM AUTHOR]

To improve the detergency of mud stains without triphosphate, we developed a new composition that enhances the detergency of mud stains more efficiently. To develop the composition, a new correction method based on the probability density functional method was used to compare the results of approximately 100 cleaning tests conducted on different days using various active ingredients. As a result of various evaluations, it was found that the combination of a homopolymer with a molecular weight of approximately 2000 and a chelating agent can effectively improve the detergency of particle stains. By combining washing experiments with different polymer concentrations, water hardness, turbidity, and reduced viscosity, we were able to estimate the expansion of the polymer and the washing mechanism using a combination of low-molecular-weight polymers and chelating agents. [ABSTRACT FROM AUTHOR]

Copyright of Oilfield Chemistry is the property of Sichuan University, Oilfield Chemistry Editorial Office and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

According to the characteristics of the high silicon tailings after flotation from cyanide tailings of a company, the solid cyanide in the tailings was studied by washing method. The single factor experiment method was used to optimize the pH value, reaction time, the type and amount of reagent, the type of eluent and the time of leaching. The results show that the chelating agent is beneficial to the washing and leaching of high silicon solid cyanide from the tailings. The optimal experimental conditions were pH = 13, adding 3 g sodium gluconate for 3 h, washing the filter cake with clean water twice, the total cyanide concentration of the high silicon tailings after treatment decreased from 653. 65 mg/kg to 27. 21 mg/kg, and the removal rate reached 95. 84%. The research results have a certain reference significance for the removal of solid cyanide from high silicon tailings. [ABSTRACT FROM AUTHOR]

The barite scale (barium sulfate) is considered one of the most common scales in oil and gas wells. Barite scale removal is crucial for flow assurance but it still represents a challenge to the oil and gas industry because of its low solubility in water and mineral acids such as HCl. Despite the huge amounts of chelating agents required to remove the barite scale, the solubility of barite (BaSO4) in these chelates is very limited. In this experimental work, a new formulation to remove the barite scale is presented with a small volume of chelating agent used and a converting agent as the main feature of the dissolver. Dissolution of BaSO4 was conducted using tetrapotassium ethylene-diamine-tetra-acetic acid (K4-EDTA) chelating agent and then obtaining the dissolution rate at 200°F to mimic the wellbore condition. The concentration of the K4-EDTA was selected based on the optimum dissolution rate of BaSO4 at 24 h of soaking time. The variation of pH was investigated using potassium base KOH at two different pH values (10.5 and 13). Converting agent concentrations were obtained based on the high solubility of the scale to the total amount of solids. As the result of the study, it was revealed that a 15 wt% concentration of potassium base EDTA with 10 wt% K2CO3 as a converting agent at high pH was highly effective in dissolving up to 100% of 3 wt% BaSO4 in less than 6 h at temperatures of 200°F and 300°F. This new formulation has proven to be a reliable and efficient solution for removing BaSO4 from wellbores and surface equipment. [ABSTRACT FROM AUTHOR]

We studied the influence of the ethylenediaminetetraacetic acid (EDTA) content used as combustion fuel when fabricating nickel oxide (NiO) nanocatalysts via solution combustion synthesis, as well as the growth behavior of carbon nanotubes (CNTs) using this catalyst. Nickel nitrate hexahydrate (Ni(NO3)2∙6H2O) was used as the metal precursor (an oxidizer), and the catalysts were synthesized by adjusting the molar ratio of fuel (EDTA) to oxidizer in the range of 1:0.25 to 2.0. The results of the crystal structure analysis showed that as the EDTA content increased beyond the chemical stoichiometric balance with Ni(NO3)2∙6H2O (F/O = 0.25), the proportion of Ni metal within the catalyst particles decreased, and only single-phase NiO was observed. Among the synthesized catalysts, the smallest crystallite size was observed with a 1:1 ratio of Ni ions to EDTA. However, an increase in the amount of EDTA resulted in excessive fuel supply, leading to an increase in crystallite size. Microstructure analysis revealed porous NiO agglomerates due to the use of EDTA, and differences in particle growth based on the fuel ratio were observed. We analyzed the growth behavior of CNTs grown using NiO nanocatalysts through catalytic chemical vapor deposition (CCVD). As the F/O ratio increased, it was observed that the catalyst particles grew excessively beyond hundreds of nanometers, preventing further CNT growth and leading to a rapid termination of CNT growth. Raman spectroscopy was used to analyze the structural characteristics of CNTs, and it was found that the ID/IG ratio indicated the highest CNT crystallinity near an F/O ratio of 1:1. [ABSTRACT FROM AUTHOR]

Background: COVID-19 has been associated with olfactory dysfunction in many infected patients. The rise of calcium levels in the nasal secretions plays an essential role in the olfaction process with a desensitization effect on the olfactory receptor neurons and a negative impact on the olfaction transmission. Ethylene diamine tetra acetic acid (EDTA) is a chelating agent that can bind free calcium in the nasal secretions, thereby reducing the adverse effects of calcium on olfactory function. Objectives: The objective of this work is to demonstrate the effect of intranasal EDTA on improving olfactory dysfunction following COVID-19. Methods: Fifty patients with a history of COVID-19 and olfactory dysfunction that persisted for more than 6 months were enrolled in the current prospective randomized clinical trial. Participants were randomized into 2 equal groups. Twenty-five patients were treated with olfactory training only, while the remaining 25 patients received treatment with olfactory training and a topical nasal spray of ethylene diamine tetra acetic acid. The olfactory function was assessed before treatment and 3 months later using the Sniffin' Sticks test. Additionally, the determination of calcium level in the nasal secretions was performed using an ion-selective electrode before treatment and 3 months later. Results: Eighty-eight percent of the patients treated with olfactory training in addition to EDTA exhibited clinical improvement, while 60% showed improvement in patients treated with olfactory training only. Furthermore, a significant decrease in the measured calcium level in the nasal secretions was demonstrated after the use of ethylene diamine tetra compared to patients treated with olfactory training only. Conclusion: Ethylene diamine tetra acetic acid may be associated with an improvement of the olfactory function post-COVID-19. [ABSTRACT FROM AUTHOR]

Composite technique of soil flushing and air sparging was frequently used to remediate the contaminated site. During these processes, the surfactant or chelating agent is bound to affect the efficiency of air sparging. In order to study the effect of the surfactant or chelating agent on the efficiency of air sparging, experiments were performed in a self-made experimental device to test the oxygen diffusion in the surfactant or chelating agent solution. First, the liquid-side mass transfer coefficient (kL) in the surfactant or chelating agent solution was measured at a free gas–liquid interface. Then the value of the diffusion coefficient of oxygen (D) was calculated based on kL, dynamic viscosity, and density of the solution. The results showed that sodium dodecyl benzene sulfonate (SDBS), rhamnolipid (RHA), triton X-100 (TX-100), saponin (SAP), ethylene diamine tetraacetic acid (EDTA), or citric acid (CA) solution presented low kL and D values compared with deionized water. The D in the surfactant solution decreased with an increase in surfactant concentration until its CMC was reached. Among different kinds of surfactant solutions, anionic surfactant and bio-surfactant presented a relatively large impact on D. Based on these results, a correlation between the D in surfactant solution and the concentration of surfactant was adopted to predict the D in surfactant solution. Regarding the influence of the chelating agent on kL and D, it was confirmed that the D decreased with the increase of EDTA or CA concentration. This effect was related to the pH and ionic strength of the chelating agent solution. [ABSTRACT FROM AUTHOR]

Marble is one of the materials most susceptible to copper leaching, resulting in easily identifiable turquoise stains on the marble. This problem is particularly relevant when we are talking about marble structures of heritage value. For this reason, conservators look for cleaning materials that are specific to the structure to be treated without damaging the original surface. Materials such as agar have been studied for a long time. Agar creates a controlled water release system that adapts to the needs of conservators who seek the greatest possible cleanliness without damaging the material to be treated. To improve the cleaning, chelating agents such as EDTA are added to the agar composition. However, the microbiological growth and the damage it produces to the original material are disadvantages to take into account. In order to solve these problems, other natural materials with cleaning potential such as kudzu and konjac gels were studied in combination with other chelating agents such as citrate, oxalate, and gluconic acid. For the characterization and evaluation of copper cleaning, various analytical techniques were used, including Raman spectroscopy, colorimetry, X-ray fluorescence (XRF), and inductively coupled plasma mass spectrometry (ICP-MS). In this study, both konjac and kudzu emerged as promising alternatives to agar, revealing distinctive features such as simplified preparation methods and inherent antimicrobial properties. The EDTA chelator was found to be the most harmful for marble surfaces, as it extracted a greater amount of calcium from the marble during application of the gels doped with it. Citrate and gluconic acid have been identified as a promising substitute to prepare doped gels for the removal of copper stains. These compounds exhibit comparable or potentially superior cleaning capabilities than EDTA, with no negative side effects. [ABSTRACT FROM AUTHOR]

In the field of stone conservation, the removal of iron stains is one of the most challenging issues due to the stability and low solubility of the ferrous species. In the present paper, three different chitosan-based hydrogels added with acetic, oxalic or citric acids are applied on different lithotypes, i.e., granite, travertine and marble, widely diffused in monumental heritages, and artificially stained by deposition of a rust dispersion. The reducing power of carboxylic acids is combined with the good chelating properties of chitosan to effectively remove rust from stone surfaces. As evidenced by colorimetry on three samples of each lithotype and confirmed by 1H-NMR relaxometry and SEM/EDS analyses, the chitosan-oxalic acid hydrogel shows the best performance and a single application of 24 h is enough to get a good restoration of the stone original features. Lastly, the chitosan-oxalic acid hydrogel performs well when a rusted iron grid is placed directly on the lithic surfaces to simulate a more realistic pollution. Current work in progress is devoted to finding better formulations for marble, which is the most challenging to clean or, with a different approach, to developing protective agents to prevent rust deposition.

Heavy metals in flue gas desulfurization (FGD) gypsum from coal-fired power plants are at risk of releaching during the processes of stockpiling and resource utilization. In this study, the effects of organosulfur chelators dithiocarbamate (DTC) and trisodium trithiocyanate-15 (TMT-15) on the solidification characteristics of heavy metals in desulphurized gypsum under different mass fractions, pH values, water contents and reaction times were investigated. The chemical composition and morphology were analyzed by inductively coupled plasma atomic emission spectrometer (ICP-AES) and scanning electron microscope (SEM). The experiments showed that both DTC and TMT-15 were effective at stabilizing the heavy metals in the FGD gypsum, with more than a 50% curing effect for all the heavy metals except Pb. DTC showed a better stabilization for Pb, Hg, Cu, Zn, and Cr, and TMT-15 showed a better curing effect for Cd. The solidified gypsum had good heavy metal stability in low-water-content environments. Increasing the mass fraction, reaction time, and pH decreased the heavy metal leaching, and the mass fraction had the greatest effect on the total heavy metal leaching concentration, followed by the reaction time and pH value.

Copyright of Journal of Agro-Environment Science is the property of Journal of Agro-Environment Science Editorial Board and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Chelating agents' application for well stimulation is gaining more and more interest, as they can perform under harsh conditions. However, the mutual influence of surfactants and chelating agents on the wettability alteration of hydrophobic carbonate rock under conditions of high-temperature well stimulation is relatively unexplored. This paper aims to study interfacial processes on the surface of hydrophobic rock in the presence of the EDTA-based chelating agent and surfactants of different classes. Cationic (cetyltrimethylammonium bromide, CTAB, and cetylpyridinium bromide, CPB), anionic (sodium dodecyl sulfate, SDS), and amhoteric (alkyldimethyl aminooxide, AO) surfactants were studied. Wettability alteration of model hydrophobic rock was studied under conditions specific to well stimulation. It was shown that chelating agent (CA) alone and its mixture with SDS could not lead to sufficient wettability alteration. CTAB, CPB, and AO were able to change the wettability effectively. A synergistic effect between CA and these surfactants was observed and a possible mechanism was proposed. AO was selected as the most promising surfactant. The influence of surfactant on the CA's dissolution capacity towards carbonate rock was investigated; dissolution capacity strongly depends on wettability alteration. Finally, the effect of CA, AO, and their mixture on the wettability of aged reservoir rock was studied and the absence of negative effects was proven. [ABSTRACT FROM AUTHOR]

Copyright of Journal of Henan Agricultural Sciences is the property of Editorial Board of Journal of Henan Agricultural Sciences and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

We evaluated the shear bond strength (SBS) of mineral trioxide aggregate (MTA) and Biodentine (BD) to coronal dentin after treatment with ethylenediaminetetraacetic acid (EDTA), phytic acid (IP6), or etidronic acid (HEDP). Sodium hypochlorite‐treated dentin surfaces were randomly divided into four groups according to conditioning protocol namely, 17% EDTA, 2.5% IP6, 9% HEDP, or distilled water (DS). Specimens were further divided according to the type of cement placed on conditioned dentin and SBS was tested. The results showed that DS/MTA and IP6/MTA groups had the highest values, and there was no significant difference between these two groups. IP6/BD group showed a lower SBS value compared to IP6/MTA; however, this did not reach the level of significance. The BS to dentin was influenced by the type of calcium silicate material and chelating agent. IP6 either improved or maintained the bonding while EDTA and HEDP showed a negative or no influence effect. [ABSTRACT FROM AUTHOR]

In this study, we focus on NiCuAl-LDH and introduce various metal ion species (Ga, Ni, Fe, Nd, Zn, Mg, and Cu) using a chelating agent into calcined NiCuAl-LDH. We obtained a maximum methanol conversion of 82.6% and H 2 yield of 53.5%. In addition, we found that the metal surface area of Ni and Cu increased compared to NiCuAl-LDH. On the other hand, results demonstrated that the presence of Ni(OH) 2 and Cu(OH) 2 on the catalyst surface had a positive effect on the MSR. We also tested the catalytic stability, introducing Cu by EDTA into calcined NiCuAl-LDH. [Display omitted] • We performed Steam reforming of methanol (MSR) with NiCuAl-LDH and LDH-M-Chelating agent. • The introduction of metals into LDH with chelating agents increases CO 2 selectivity and H 2 yield. • Presence of Ni(OH) 2 and Cu(OH) 2 on the catalyst surface has a positive effect on the MSR. • The effect of reaction temperature on MSR and catalyst stability in MSR were also studied. [ABSTRACT FROM AUTHOR]

In order to improve the surface quality of tantalum wafer after chemical mechanical polishing (CMP), the effects of the particle size of nano-silica sol, type and mass fraction of chelating agent (i.e. glycine and disodium ethylenediaminetetraacetate), and mass fraction of oxidant (hydrogen peroxide) on the electrochemical behavior and removal rate of tantalum wafer, and its surface quality after polishing were studied by electrochemical testing and CMP experiments. The results showed that the removal rate of tantalum wafer was 71 nm/min when being polished in a slurry comprising 40% of nanosilica sol with an average particle size of 50 nm as abrasive, 1.0% of disodium ethylenediaminetetraacetate as chelating agent, and 1.0% of hydrogen peroxide as oxidant. The surface of polished tantalum wafer was free of orange peel and scratch. [ABSTRACT FROM AUTHOR]

Protein–protein and protein–mineral interactions can result in defects, such as sedimentation and age gelation, during the storage of high-protein beverages. It is well known that age gelation can be delayed by adding cyclic polyphosphates such as sodium hexametaphosphate (SHMP). This study aims to assess the influence of different phosphate chain lengths of SHMP on the physicochemical properties of high-protein dispersions. The effect of adding different SHMP concentrations at 0%, 0.15%, and 0.25% (w/w) before and after heating of 6%, 8%, and 10% (w/w) milk protein concentrate dispersions was studied. The phosphate chain lengths of SHMPs used in this study were 16.47, 13.31, and 9.88, and they were classified as long-, medium-, and short-chain SHMPs, respectively. Apparent viscosity, particle size, heat coagulation time (HCT), color, and turbidity were evaluated. It was observed that the addition of SHMP (0.15% and 0.25%) increased the apparent viscosity of MPC dispersions. However, the chain length and the concentration of the added SHMP had no significant (p > 0.05) effect on the apparent viscosity after heating the dispersions. The HCT of a dispersion containing 6%, 8%, and 10% protein with no SHMP added was 15.28, 15.61, and 11.35 min, respectively. The addition of SHMP at both levels (0.15% and 0.25%) significantly increased the HCT. Protein dispersions (6%, 8%, and 10%) containing 0.25% short-chain SHMP had the highest HCT at 19.29, 19.61, and 16.09 min, respectively. Therefore, the chain length and concentration of added SHMP significantly affected the HCT of unheated protein dispersion (p < 0.05).

Polysaccharides are functional foods or drugs that can be used to alleviate heavy metal poisoning by cadmium, lead, mercury, and arsenic. Industries generate substantial quantities of toxic heavy metal wastes, such as wastewater discharges, paints, electronic waste, batteries, pigments, and plastics, into the environment that pose a risk to human health. Therefore, it is imperative to eliminate accumulated heavy metal ions from the body and the environment. Heavy metal toxicity can lead to decreased energy levels and impair the functioning of vital organs, such as the brain, lungs, kidneys, liver, and blood. Prolonged exposure can result in progressive physical, muscular, and neurological degeneration that resembles conditions such as multiple sclerosis, Parkinson’s disease, Alzheimer’s disease, and muscular dystrophy. Polysaccharides operate through mechanisms such as chelation, antioxidant defense, immunomodulation, and tissue repair. Polysaccharides involved in heavy metal removal include methionine and cysteine, together with N-acetylcysteine, an acetylated form of cysteine, S-adenosylmethionine, a metabolite of methionine, α-lipoic acid, and the tripeptide glutathione (GSH). These compounds effectively bind with harmful heavy metals to create a stable complex and defend biological targets from metal ions, thus decreasing their harmful effects and causing them to be excreted from the body. This review also highlights the importance of polysaccharides’ ability to mitigate oxidative stress, enhance immune responses, and support tissue repair processes. Polysaccharides are ubiquitous in nature and take part in diverse processes, making them potential natural therapies for heavy metal-related diseases. This review discusses the effectiveness of natural polysaccharides and the mechanisms that allow them to bind with heavy metals to alleviate their effects from the body and the environment. Polysaccharides have inherent features that enable them to function as pharmacological agents and regulate the immune response.

The aim of this study was to determine an appropriate chelating agent for Q stage in the TCF bleaching sequence of soda-oxygen, soda, soda-anthraquinone and alkaline-sulfite wheat straw pulps prior to P bleaching stage. In order to study the possible effect of chelating agents, three different chelating agents (EDTA, DTPA and DTMPA) were used. To evaluate the impact of transition metal ions on P stage, the residual Mn, Fe and Cu ion concentrations were determined with atomic absorption spectrometry. Ash and silica contents of pulps have been determined for each chelating agent, separately. FTIR-ATR spectroscopy was used to demonstrate the bleaching effect. The results showed that the most appropriate chelating agents varied depending on the type of pulp. The best chelating effect was achieved with DTMPA for soda-oxygen pulp, EDTA for both soda and alkaline-sulfite pulps, and DTPA for soda-anthraquinone pulp. [ABSTRACT FROM AUTHOR]