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Objective: This study aimed to assess the efficacy of different oral iron preparations prescribed for prevention of iron deficiency anemia in healthy infants. Methods: This retrospective study enrolled infants aged between 6 and 12 months who were initiated on iron prophylaxis at four months of age. Enrolled children consistently used specific iron preparations (ferrous, ferric or liposomal iron) and had their complete blood counts and serum ferritin levels assessed within the 6–12 month timeframe. Blood values and iron prophylaxis type (ferrous (Fe+2), ferric (Fe+3), liposomal iron) were recorded. Chi-square test was used to compare the hemoglobin and ferritin levels levels between groups. Univariate and multivariate regression analyses assessed the risk of anemia. Results: The study included 371 children (ferrous sulphate - 60, iron hydroxide-polymaltose complex - 137 and liposomal ferric pyrophosphate - 174) with a mean (SD) age 9.1 (1.3) mo. Iron deficiency in different groups were: liposomal iron (46.0%), ferric iron (44.5%), and ferrous iron (5.0%). Mean (SD) serum ferritin levels (µg/L) were higher in the ferrous group [30.1 (10.8)] compared to infants receiving ferric [17.6 (14.50)] and liposomal iron [15.4 (12.1)] (P < 0.001). Mean (SD) hemoglobin levels (g/dL) were significantly higher in the ferrous group [12.4 (0.8)] compared to ferric [11.9 (1.1)] and liposomal iron group [12.0 (1.1)]; P =0.008. Multiple regression analysis showed that ferrous group was associated with a lower risk of iron deficiency [OR (95% CI) 0.04 (0.01–0.15), P < 0.001]. Conclusion: Ferrous iron demonstrated superior efficacy compared to ferric and liposomal iron. Further studies are needed to establish alternative iron preprations in children. [ABSTRACT FROM AUTHOR]

The growing challenges of reducing exhaust emissions and improved fuel economy has triggered automotive engineers to design and manufacture engine parts with superior mechanical properties and dimensional accuracies. Valve guides are cylindrical structures supporting inlet valve and exhaust valve stems during operation. Conventionally made of grey cast iron material, valve guide suffers from severe wear losses leading to loss of fuel and increased emissions due to improper valve stem seating. Here, the synthesis of a novel ferrous powder metallurgy composite is presented and wear characteristics have been studied at varying loads of 30 N, 40 N and 50 N and varying sliding speeds of 0.5 m/s, 1 m/s and 2 m/s under lubricated conditions. The samples have undergone nitriding heat treatment at 1150 °C to improve surface hardness to 700 Hv. The samples have shown negative wear rates due to high hardness and capillary action of lubricating oil and exhibited stable friction coefficient values. This has been attributed to the formation of hard phases Fe2N, Fe3N, and Fe4N and Fe(Mn)3C and twinning-induced plastic compounds like (Fe24Mn) 0.08 as evident from XRD analysis. The morphological analysis of worn out samples was done with SEM Coupled with EDS and it showed micro-cutting, Ploughing, and delamination as main wear phenomenon.

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Introduction: The performance functionality efficacy of the engine’s valve train assembly is considerably affected by the valve guide. Material selection is impacted by the prolonged operational lifespan of engines, which favours casting and machining materials such as cast iron. The intent of this study is to examine the dry sliding characteristics of GG25 cast iron with copper additives. Discovering the ways in which variations in load and sliding velocity impact wear characteristics is of paramount significance. Methods: The research entailed the examination of wear characteristics across various environmental conditions. Loads were varied at 30 N, 40 N, and 50 N while maintaining a 1 m/s velocity constant. In the same manner, sliding velocities of 0.5 m/s, 1 m/s, and 2 m/s were varied while a constant load of 30 N was maintained. Experimental techniques were carried out at ambient temperature. Throughout the investigations, frictional forces and the coefficient of friction were also determined. The wear mechanisms of samples that had become deteriorated or worn-out were examined by employing a scanning electron microscope when combined with EDX analysis. Results: A rise in the normal load from 30 N to 40 N led to a twofold rise in wear losses, measuring 417 microns as compared with 222 microns previously. The range of wear losses observed at moderate speeds (0.5 m/s–1 m/s) was 133–222 microns. Conversely, the maximum wear loss observed was 1,226 microns at elevated sliding velocities of 2 m/s, in contrast to 617 microns at higher normal loads of 50 N. Additionally, the research discovered that normal load is more pronounced when both loading and speed are moderate, whereas sliding speed becomes more substantial when both are raised, culminating to higher wear losses. Discussions: In summary, the research highlights the considerable effect that normal load and sliding speed have on the prevalence of wear losses. In conditions of moderate loading and velocity, the influence of normal load is more significant. However, as sliding accelerates, it becomes the predominant factor. An analysis of frictional forces as well as the coefficient of friction indicated that under loading conditions of 30 N–50 N, the friction coefficient raised from 0.238 to 0.43. The wear mechanisms, as discerned via scanning electron microscopy and EDX analysis, underscored the considerable impact of increased sliding velocity on wear loss in comparison to conditions of higher loading. [ABSTRACT FROM AUTHOR]

Introduction: The performance functionality efficacy of the engine’s valve train assembly is considerably affected by the valve guide. Material selection is impacted by the prolonged operational lifespan of engines, which favours casting and machining materials such as cast iron. The intent of this study is to examine the dry sliding characteristics of GG25 cast iron with copper additives. Discovering the ways in which variations in load and sliding velocity impact wear characteristics is of paramount significance.Methods: The research entailed the examination of wear characteristics across various environmental conditions. Loads were varied at 30 N, 40 N, and 50 N while maintaining a 1 m/s velocity constant. In the same manner, sliding velocities of 0.5 m/s, 1 m/s, and 2 m/s were varied while a constant load of 30 N was maintained. Experimental techniques were carried out at ambient temperature. Throughout the investigations, frictional forces and the coefficient of friction were also determined. The wear mechanisms of samples that had become deteriorated or worn-out were examined by employing a scanning electron microscope when combined with EDX analysis.Results: A rise in the normal load from 30 N to 40 N led to a twofold rise in wear losses, measuring 417 microns as compared with 222 microns previously. The range of wear losses observed at moderate speeds (0.5 m/s–1 m/s) was 133–222 microns. Conversely, the maximum wear loss observed was 1,226 microns at elevated sliding velocities of 2 m/s, in contrast to 617 microns at higher normal loads of 50 N. Additionally, the research discovered that normal load is more pronounced when both loading and speed are moderate, whereas sliding speed becomes more substantial when both are raised, culminating to higher wear losses.Discussions: In summary, the research highlights the considerable effect that normal load and sliding speed have on the prevalence of wear losses. In conditions of moderate loading and velocity, the influence of normal load is more significant. However, as sliding accelerates, it becomes the predominant factor. An analysis of frictional forces as well as the coefficient of friction indicated that under loading conditions of 30 N–50 N, the friction coefficient raised from 0.238 to 0.43. The wear mechanisms, as discerned via scanning electron microscopy and EDX analysis, underscored the considerable impact of increased sliding velocity on wear loss in comparison to conditions of higher loading.

Abstract Background Biofilms play a role in recalcitrance and treatability of bacterial infections, but majority of known antibiotic resistance mechanisms are biofilm-independent. Biofilms of Pseudomonas aeruginosa, especially in cystic fibrosis patients infected with the alginate producing strains in their lungs, are hard to treat. Changes in growth-related bacterial metabolism in biofilm affect their antibiotic recalcitrance which could be considered for new therapies designed based on these changes. In this study, effects of nitrate, arginine, and ferrous were investigated on antibiotic recalcitrance in alginate-encapsulated P. aeruginosa strains isolated from cystic fibrosis patients in the presence of amikacin, tobramycin, and ciprofloxacin. Also, expression of an efflux pump gene, mexY, was analyzed in selected strains in the presence of amikacin and ferrous. Methods Clinical P. aeruginosa strains were isolated from cystic fibrosis patients and minimum inhibitory concentration of amikacin, tobramycin, and ciprofloxacin was determined against all the strains. For each antibiotic, a susceptible and a resistant or an intermediate-resistant strain were selected, encapsulated into alginate beads, and subjected to minimal biofilm eradication concentration (MBEC) test. After determining MBECs, sub-MBEC concentrations (antibiotics at concentrations one level below the determined MBEC) for each antibiotic were selected and used to study the effects of nitrate, arginine, and ferrous on antibiotic recalcitrance of encapsulated strains. Effects of ferrous and amikacin on expression of the efflux pump gene, mexY, was studied on amikacin sensitive and intermediate-resistant strains. One-way ANOVA and t test were used as the statistical tests. Results According to the results, the supplements had a dose-related effect on decreasing the number of viable cells; maximal effect was noted with ferrous, as ferrous supplementation significantly increased biofilm susceptibility to both ciprofloxacin and amikacin in all strains, and to tobramycin in a resistant strain. Also, treating an amikacin-intermediate strain with amikacin increased the expression of mexY gene, which has a role in P. aeruginosa antibiotic recalcitrance, while treating the same strain with ferrous and amikacin significantly decreased the expression of mexY gene, which was a promising result. Conclusions Our results support the possibility of using ferrous and arginine as an adjuvant to enhance the efficacy of conventional antimicrobial therapy of P. aeruginosa infections.

Naturally occurring Fe(III) films with rainbow reflection iridescence have been observed floating on the water surface of various spots covered with shallow water (e.g., edges of wetlands and creeks, standing water over soils). This natural phenomenon has become a scenic attraction and stimulated much curiosity. We pursued an experimental inquiry aimed at probing this interesting, curious natural wonder. As the first critical task, floating Fe(III) films were successfully generated in an assessable, controllable setting in our laboratory. This enabled us to establish this phenomenon reproducibly under controlled conditions and characterize the phenomenon over the entire span of the formation and transformation of the Fe(III) films. Our film generation method requires a few things: fresh soil (source for Fe(III) and microbes), glucose (energy source), and water in a container. The floating Fe(III) films as observed in the field occurred in ~1–3 day(s) on the water surface of the inundated soil mixed with the sugar. The Fe(III) films then grew from initial very thin, colorless, somewhat transparent films with rainbow reflection iridescence to colored thicker films and then to orange/orange-red/red crusts over the time. A comprehensive mechanistic picture was formulated to depict the formation of the Fe(III) films. Several sequential processes are operative. First, the Fe(III) (oxides, oxyhydroxides) in the soil is reduced to Fe(II) by the Fe(III)-reducing microbes during their anerobic respiration with Fe(III) as the electron (e−) acceptor after depletion of dissolved O2 in the water as a result of aerobic microbial respiration with O2 as the e− acceptor. The Fe(II), being soluble, then diffuses to the water surface where it is oxidized to Fe(III). Subsequently, the Fe(III) hydrolyzes and various Fe(III) hydrolysis products polymerize to stabilize. A polymeric model was created to account for the Fe(III) film transformation. The Fe(III) films are considered to transform from the dimers and trimers and linear polymers of Fe(OH)3 to Fe(III) polymer sheets (e.g., Fe(OH)3, FeOOH), to 3D Fe(III) polymers, and eventually to Fe2O3 colloid particles. This floating Fe(III) film phenomenon boasts an environmental chemical drama of redox cycling of Fe(III)/Fe(II) at soil/water and water/air interfaces coupled with Fe(II) transport from the inundated soil to the water surface followed by ultimate mineralization of the Fe(III) polymers. Our Fe(III) film generation method can be readily scaled up to supply Fe(III) films of rich varieties in thickness, size, morphology, and structure over the entire span of various stages of their formation and transformation as desired for various uses. This setup offers a platform needed for further controlled studies on the kinetics, mechanism, and process of abiotic and biotic nature involved in the Fe(III) film phenomenon and for exploration of versatile roles of the Fe(III) films as nanofilms in Fe(III)/Fe(II)-surface catalyzed chemical and photochemical reactions involving various natural and synthetic compounds.

Background: Biofilms play a role in recalcitrance and treatability of bacterial infections, but majority of known antibiotic resistance mechanisms are biofilm-independent. Biofilms of Pseudomonas aeruginosa, especially in cystic fibrosis patients infected with the alginate producing strains in their lungs, are hard to treat. Changes in growth-related bacterial metabolism in biofilm affect their antibiotic recalcitrance which could be considered for new therapies designed based on these changes. In this study, effects of nitrate, arginine, and ferrous were investigated on antibiotic recalcitrance in alginate-encapsulated P. aeruginosa strains isolated from cystic fibrosis patients in the presence of amikacin, tobramycin, and ciprofloxacin. Also, expression of an efflux pump gene, mexY, was analyzed in selected strains in the presence of amikacin and ferrous. Methods: Clinical P. aeruginosa strains were isolated from cystic fibrosis patients and minimum inhibitory concentration of amikacin, tobramycin, and ciprofloxacin was determined against all the strains. For each antibiotic, a susceptible and a resistant or an intermediate-resistant strain were selected, encapsulated into alginate beads, and subjected to minimal biofilm eradication concentration (MBEC) test. After determining MBECs, sub-MBEC concentrations (antibiotics at concentrations one level below the determined MBEC) for each antibiotic were selected and used to study the effects of nitrate, arginine, and ferrous on antibiotic recalcitrance of encapsulated strains. Effects of ferrous and amikacin on expression of the efflux pump gene, mexY, was studied on amikacin sensitive and intermediate-resistant strains. One-way ANOVA and t test were used as the statistical tests. Results: According to the results, the supplements had a dose-related effect on decreasing the number of viable cells; maximal effect was noted with ferrous, as ferrous supplementation significantly increased biofilm susceptibility to both ciprofloxacin and amikacin in all strains, and to tobramycin in a resistant strain. Also, treating an amikacin-intermediate strain with amikacin increased the expression of mexY gene, which has a role in P. aeruginosa antibiotic recalcitrance, while treating the same strain with ferrous and amikacin significantly decreased the expression of mexY gene, which was a promising result. Conclusions: Our results support the possibility of using ferrous and arginine as an adjuvant to enhance the efficacy of conventional antimicrobial therapy of P. aeruginosa infections. [ABSTRACT FROM AUTHOR]

Highly efficient azo-day quinazolinone derivatives carrying a π bond and OH electron donor groups have been designed, synthesized, and evaluated as colorimetric chemosensors for detecting metal ions in biological and environmental samples, which was further supported by the DFT studies and UV–vis titration experiment. The 3-amino-2-styrylquinazolin-4(3H)-one (1) was directed to react with phenols during a diazotization type reaction to form a series of azo-day 3-(diazenyl)-2-(styryl)quinazolin-4(3H)-one (4a-e), which could not only have been confirmed by FTIR, H1NMR, C13NMR, Ms and elemental analysis but could also be easily used for the detection of metal ions. Compound 4c exhibited a rapid qualitative and quantitative method for the detection of CoII at λ max (582 nm) and FeII at λ max (566 nm) in an aqueous solution. The current study introduces a facile, low cost, more specific and selective chemosensor for detecting trace amounts of cobalt and ferrous ions.

Experiments for simultaneous elimination and detoxification of microgram level of As(Ⅲ) in the presence of micromolar H2O2 and Fe(Ⅱ) which are frequently encountered in natural water were conducted. The results showed that the molar ratio of oxidant to As(III) plays important role in As(III) oxidation under the experimental conditions. The extent of As(Ⅲ) oxidation with single H2O2 or Fe(Ⅱ) ranged from 7.9 % to 60.3 % and 22.2–46.6 %, respectively. Treatments with H2O2/As(Ⅲ) molar ratios in the range 150: 1–750: 1 or Fe(Ⅱ)/As(Ⅲ) molar ratios in the range 37.5: 1–375: 1 were more favor for As(Ⅲ) oxidation respectively, and increasing oxidant concentration did not result in complete As(Ⅲ) oxidation. As(Ⅲ) was completely oxidized and eliminated following the precipitation of ferric hydroxides in 5 reaction minutes when H2O2 and Fe(Ⅱ) coexisted in the reaction system. The interface characterization for the reacted precipitates after the experiment were conducted by using a high-resolution field emission scanning electron microscopy (SEM) coupled with an EX-350 energy dispersive X-ray spectrometer (EDX) and X-ray photoelectron spectroscopy (XPS), respectively. The results showed that As(Ⅴ) was the merely arsenic species and As oxide primary situated in the subsurface layer of the reacted precipitates, whereas Fe was more concentrated in the outermost surface layer. Our research showed that H2O2 and Fe(Ⅱ) at natural level may exert significant influence on arsenic mobilization in natural water. Considering the much more toxic of As(Ⅲ) than that of As(Ⅴ), the research also provide us an environmental friendly choice in the elimination and detoxification of microgram As(Ⅲ) in drinking water.

Coal fly ash (CFA) is one of the major pollutants around the whole world. At the same time, incense stick ash (ISA) is another waste that is generated in huge amounts in Southeast Asia. Both of these wastes are rich in different types of minerals; for instance, CFA is rich in alumina, silica, and ferrous, while incense sticks ash is rich in calcium and silica. ISA has intermediate to trace amounts of ferrous, alumina, and magnesium. The addition of alkali-rich materials with high Al and Si-containing CFA helps in the formation of zeolites or geopolymers. So, in the current research work, the authors have prepared a CFA: ISA mixture in the ratio of 1:1, followed by mixing them with NaOH, CaOH2, and KOH in a dry state in a crucible. Further, all these mixtures were then calcined at 600 °C for six hours in a muffle furnace. Further, the developed products were analyzed by various sophisticated instruments for detailed information. Finally, the developed material's potential was assessed for the remediation of malachite green from the aqueous solution by batch adsorption study. The developed adsorbents efficiently removed the dye from the aqueous solutions within one hour. The kinetic study revealed that the dye removal followed a pseudo-second-order reaction. Finally, the developed material was also assessed for its suitability as an adsorbent by observing the effect of leaching of potassium, aluminum, and silica from the adsorbent surface into the water systems. Such approaches will solve the problem of solid waste disposal arising from both the ashes. [ABSTRACT FROM AUTHOR]

[Display omitted] • SOM significantly inhibited TCS and NPS degradation in the Fe2+/PS system. • Molecular properties of the three PPCPs determined their reactivity with oxidants. • SO 4 •− and 1O 2 played major roles in TCS and NPS degradation in different soils. • Soil surface functional groups possibly consumed •OH and 1O 2 , and generated SO 4 •−. • Soil types affected the degradation pathways of TCS and NPS in different soils. Pharmaceuticals and personal care products (PPCPs) are widely used worldwide and cause potential soil pollution. Fe2+-activated persulfate (PS) processes (Fe-PAPs) are promising techniques for soil remediation. However, a knowledge gap exists in the mechanistic insights into the dominant factors affecting the degradation of different PPCPs in varied soil types. This study systematically investigated the roles of soil components and pollutant properties in the degradation of three PPCPs (triclosan (TCS), triclocarban (TCC), and naproxen (NPS)) in the nine soils in the Fe2+/PS system. The degradation efficiencies of TCS and NPS ranged from 10.92 % to 91.62 % and 46.59 % to 99.81 %, respectively, whereas nearly no degradation was observed for TCC. PPCPs with high water solubility, high energies of the highest occupied molecular orbital (E HOMO), low p K a values, low energy gap (ΔE), or low vertical ionization potential (VIP) were more favorable for degradation. XPS analysis suggested that aliphatic carbon (Ali–C–C(H)), ether or alcohol carbon (C–O), and aldehyde or ketonic carbon (C O) on SOM significantly inhibited TCS degradation. The results of ROS quenching experiments showed that SO 4 •− and 1O 2 played major roles in TCS and NPS degradation in the six soils, with the relative contributions ranged from 24.82 % to 99.14 % and 0.15 % to 73.40 %, respectively. The interaction between soil components, active species, and pollutants resulted in the distinct intermediates of TCS and NPS in different soils. Our findings provide in-depth insights into the role of soil composition and pollutant properties on the remediation of PPCP-contaminated soils in Fe-PAPs. [ABSTRACT FROM AUTHOR]

This paper is devoted to the memory of Professor Ljubomir Nedeljkovic (1933-2020), Head of the Department of Iron and Steel Metallurgy University of Belgrade, Serbia. Assessment of the melt quality is one of the most important casting process parameters, which allowed sound production of intricated cast parts. At the present time, various devices have been applied at foundry floors to control melt quality. Thermal analysis is one of them, widely used for melt quality control in ferrous and non-ferrous casting plants. During solidification, metal and alloys released latent heat, which magnitude is dependent on the type of phases that form during the solidification process. Plotting temperature versus time data during solidification provides useful information related to the actual solidification process. The applied technique is called thermal analysis, whereas the cooling curve is the name of such a plot. The main aim of this paper is to give a short overview of the present thermal analysis application in various foundries and to indicate the future potential use of this technique.

ABSTRACT Pseudomonas aeruginosa is an opportunistic pathogen that has been declared by the World Health Organization as a “priority 1 critical pathogen” needing immediate new strategies for chemotherapy. During infection, P. aeruginosa uses redundant mechanisms to acquire ferric, heme (Hm), or ferrous iron from the host to survive and colonize. Significant efforts have been undertaken to develop siderophore blockers to inhibit ferric iron acquisition by P. aeruginosa, but there is a lack of inhibitors that can block Hm or ferrous iron acquisition by P. aeruginosa. We developed and employed a targeted high-throughput screen (HTS) and identified a molecule(s) that can specifically inhibit the Hm and ferrous iron acquisition systems of P. aeruginosa. Our targeted approach relies on screening a small-molecule library against P. aeruginosa under three growth conditions, where the only variable was the iron source (ferric, Hm, or ferrous iron). Each condition served as a counterscreen for the other, and we identified molecules that inhibit the growth of P. aeruginosa in the presence of only Hm or ferrous iron. Our data indicate that econazole, bithionate, and raloxifene inhibit the growth of P. aeruginosa in the presence of Hm and that oxyquinoline inhibits the growth of P. aeruginosa in the presence of ferrous iron. These iron-specific inhibitors do not interfere with the activity of meropenem, a commercial antipseudomonal, and can also increase meropenem activity. In conclusion, we present a proof of concept of a successful targeted conditional screening method by which we can identify specific iron acquisition inhibitors. This approach is highly adaptable and can easily be extended to any other pathogen. IMPORTANCE Since acquiring iron is paramount to P. aeruginosa’s survival and colonization in the human host, developing novel strategies to block the access of P. aeruginosa to host iron will allow us to starve it of an essential nutrient. P. aeruginosa uses siderophore, heme, or ferrous iron uptake systems to acquire iron in the human host. We have developed a novel approach through which we can directly identify molecules that can prevent P. aeruginosa from utilizing heme or ferrous iron. This approach overcomes the need for the in silico design of molecules and identifies structurally diverse biologically active inhibitor molecules. This screening approach is adaptable and can be extended to any pathogen. Since Gram-negative pathogens share many similarities in iron acquisition at both the mechanistic and molecular levels, our screening approach presents a significant opportunity to develop novel broad-spectrum iron acquisition inhibitors of Gram-negative pathogens.

Fly ash or coal fly ash causes major global pollution in the form of solid waste and is classified as a “hazardous waste”, which is a by-product of thermal power plants produced during electricity production. Si, Al, Fe Ca, and Mg alone form more than 85% of the chemical compounds and glasses of most fly ashes. Fly ash has a chemical composition of 70–90%, as well as glasses of ferrous, alumina, silica, and CaO. Therefore, fly ash could act as a reliable and alternative source for ferrous, alumina, and silica. The ferrous fractions can be recovered by a simple magnetic separation method, while alumina and silica can be extracted by chemical or biological approaches. Alumina extraction is possible using both alkali- and acid-based methods, while silica is extracted by strong alkali, such as NaOH. Chemical extraction has a higher yield than the biological approaches, but the bio-based approaches are more environmentally friendly. Fly ash can also be used for the synthesis of zeolites by NaOH treatment of variable types, as fly ash is rich in alumino-silicates. The present review work deals with the recent advances in the field of the recovery and synthesis of ferrous, alumina, and silica micro and nanoparticles from fly ash.

Coal fly ash (CFA) is one of the major pollutants around the whole world. At the same time, incense stick ash (ISA) is another waste that is generated in huge amounts in Southeast Asia. Both of these wastes are rich in different types of minerals; for instance, CFA is rich in alumina, silica, and ferrous, while incense sticks ash is rich in calcium and silica. ISA has intermediate to trace amounts of ferrous, alumina, and magnesium. The addition of alkali-rich materials with high Al and Si-containing CFA helps in the formation of zeolites or geopolymers. So, in the current research work, the authors have prepared a CFA: ISA mixture in the ratio of 1:1, followed by mixing them with NaOH, CaOH2, and KOH in a dry state in a crucible. Further, all these mixtures were then calcined at 600 °C for six hours in a muffle furnace. Further, the developed products were analyzed by various sophisticated instruments for detailed information. Finally, the developed material’s potential was assessed for the remediation of malachite green from the aqueous solution by batch adsorption study. The developed adsorbents efficiently removed the dye from the aqueous solutions within one hour. The kinetic study revealed that the dye removal followed a pseudo-second-order reaction. Finally, the developed material was also assessed for its suitability as an adsorbent by observing the effect of leaching of potassium, aluminum, and silica from the adsorbent surface into the water systems. Such approaches will solve the problem of solid waste disposal arising from both the ashes.

Ferrous (Fe (II)) plays a key role in the production or consumption of N 2 O through biochemical pathways in paddy soil. Drying-wetting alternations can affect Fe cycling and the associated N 2 O emissions, however, the underlying microbial mechanisms remain largely unknown, particularly in plant systems with the presence of roots. In this study, a laboratory experiment with four Fe (II) levels (0, 50, 150, and 300 mg Fe (II) kg−1 dry soil) was conducted to investigate the response of N 2 O emission and denitrifying genes to iron (II) supplement in root zone and bulk region during wetting-drying cycles in paddy soils. The results indicated that supplemented Fe (II) led to a reduction in soil N 2 O emissions, predominantly observed during the drying phase. The bulk soil exhibited higher N 2 O fluxes compared to root zone. However, the decrease in cumulative N 2 O (cumul-N 2 O) by Fe (II) was significantly greater in bulk region than in root-affected soil (P < 0.001), registering 85–91 % reduction for soils amended with low to medium rates (50 and 150 mg Fe (II) kg−1 dry soil) throughout the experiment. This might be attributed to the more sensitive response of N 2 O reductase (nosZ gene) to low or medium Fe (II) supplementation in bulk soil than in root zone. The highest Fe (II) addition (300 mg Fe (II) kg−1 dry soil) showed a negative impact on nosZ -containing gene during initial flooding phase, resulting in the lower reduction rate (40 %) in cumulative N 2 O emission from bulk soil. Cross-correlation analysis showed that the changes of nosZ- containing genes in root zone occurred before variations of cumulative N 2 O data, indicating that compared to bulk soil, root zone soil exhibited a more pronounced of N 2 O consumption capability, especially after addition of ferrous. In summary, judicious Fe (II) application into soil promotes N 2 O reduction during wetting-drying alternation. The response of nosZ abundance to Fe (II) supplementation is likely the pivotal microbial factor influencing N 2 O emission reduction during wetting-drying alternation in paddy soil. [Display omitted] • Addition of Fe(II) into paddy soil reduced N 2 O emission during wetting-drying alternation. • Supplemented Fe(II) significantly increased nosZ gene from paddy soil during drying. • The root zone in rice-planted paddy soil might have the stronger capacity of N 2 O consumption. • Relations between N 2 O emission and abundance of denitrifying genes often existed with time lags. [ABSTRACT FROM AUTHOR]

Restoration of submerged macrophytes is an efficient way for endogenous nutrient control and aquatic ecological restoration, but slow growth and limited reproduction of submerged macrophytes still exist. In this research, the effect of ferrous on the seed germination and growth of Vallisneria natans (V. natans) were studied through aquatic simulation experiments and its influence on the rhizosphere microbial community was also explored. The seed germination, growth, and physiological and ecological parameters of V. natans were significantly affected by the ferrous treatments. Ferrous concentration above 5.0 mg/L showed significant inhibition of seed germination of V. natans and the best concentration for germination was 0.5 mg/L. During the growth of V. natans, after ferrous was added, a brief period of stress occurred, which then promoted the growth lasting for about 19 days under one addition. The diversity and richness of the rhizospheric microbial were increased after the ferrous addition. However, the function of the rhizospheric microbial community showed no significant difference between different concentrations of ferrous adding in the overlying water. Ferrous addition affected the growth condition of plants (content of CAT, Chl a , Chl b , etc.), thus indirectly affecting the rhizospheric microbial community of V. natans. These impacts on V. natans and rhizosphere microorganisms could generalize to other submerged macrophytes in freshwater ecosystems, particularly which have similar habits. These findings would contribute to the ecological evaluation of ferrous addition or iron-containing water, and provide a reference for submerged macrophytes restoration and ecological restoration in freshwater ecosystems. [Display omitted] • 0.5 mg/L ferrous addition significantly improved the germination of V. natans seeds. • Ferrous addition contributed to promoting growth and leaf chlorophyll content. • The diversity and richness of rhizosphere microbes of V. natans were increased. • Addition ferrous can be utilized in promoting submerged macrophytes restoration. [ABSTRACT FROM AUTHOR]

[Display omitted] • The Fe2+/OA/PS system was efficient over a wide pH range. • Exogenous Fe2+ and Fe3+ dissolved from soil participated in PS activation. • CO 2 •- radicals contributed to the reduction of Fe3+/Fe3+-OA. • TCS degradation pathways were proposed in the Fe2+/OA/PS system. • Column experiments simulated TCS in-suit remediation in the Fe2+/OA/PS system. Triclosan (TCS) is a compound in pharmaceutical and personal care products (PPCPs) that preferentially accumulates in soil and may threaten human health. Iron-based persulfate activation processes (Fe-PAPs) are a promising technique in soil remediation but are limited by their narrow pH application range and resultant iron precipitation. In this study, oxalic acid (OA) was specifically introduced to improve the efficiency of Fe2+-activated persulfate (PS) processes for TCS degradation in soil. The complexation of OA and Fe2+ improved the total iron concentration in the Fe2+/OA/PS system and prevented iron precipitation. Fe-minerals in soil were also dissolved by OA, which participated in PS activation. The most appropriate proportion of Fe2+/OA/PS is 1:1:1, and approximately 85% of the TCS was degraded within 240 min compared with 45% in the Fe2+/PS system. SO 4 •- and 1O 2 played important roles on TCS oxidation, while O 2 •- and CO 2 •- mainly participated in the iron cycle. The weak stretch of Fe-O in OA containing treatments in ATR-FTIR measurements provided evidence that OA dissolved the Fe-minerals. The introduction of OA in the Fe2+/PS system in four different soils reduced the negative effect of soil organic matter on TCS degradation. Three types of intermediates including hydroxylation, cleavage of ether bonds and cyclization products, were identified by LC-Q-TOF-MS. Column experiments were used to study the feasibility of in situ chemical oxidation (ISCO) remediation of TCS in the Fe2+/OA/PS system. Our findings indicated the ability of OA to be used as a cheating agent in Fe-PAPs for TCS soil remediation. [ABSTRACT FROM AUTHOR]

A study of the pretreatment stage and subsequent leaching of a mixed copper ore with different chloride solutions containing iron was carried out. The first stage considered pretreatment tests to decide the best conditions. Two levels of each factor were analyzed, 20 and 50 kg/t of NaCl, 17 and 25 kg/t of H2SO4, 0 and 25 kg/t of Fe2(SO4)3·9.2H2O, 0 and 25 kg/t of Fe2SO4·7H2O, and a curing time of 15 and 30 days. The results showed a significant effect of NaCl and curing time on the extraction, and less effect was found with the variation of acid and iron salts. The second stage included column leaching using a solution with 0.5 g/L of Cu+2, 80 g/L of Cl−, 10 g/L of H2SO4, and variable concentrations of ferric and ferrous ions (0 and 2 g/L). The best copper extraction of 80.2% was found considering a pretreatment of 30 days, 25 kg/t of H2SO4, 50 kg/t of NaCl, and a leaching solution concentration described previously with 2 g/L of Fe+2. The results showed the leaching of all copper oxide species and 20% of the copper sulfide species. In addition, there was a reduction in the acid consumption as the resting time increases. Furthermore, to evaluate a possible decrease in time and acid in pretreatment and chloride in leaching, tests including 10 and 25 kg/t of H2SO4 and 1, 15, and 30 days of curing and a diminution of the NaCl concentration to 20 g/L (content from seawater) were executed. The results showed a significant effect on curing time below 15 days. Furthermore, the slight influence of the decrease of acid on copper extraction gives cost reduction opportunities. The diminution of chloride concentration (80 to 20 g/L) in leaching solution decreases the extraction from 79% to 66.5%. Finally, the Mellado leaching kinetic model was successfully implemented.

In this work, the removal of arsenic from aqueous solution by using FeSO 4 with CaCO 3 was investigated. Arsenic removal was significantly improved in the presence of CaCO 3 , compared with Ca(OH) 2 , giving an arsenic removal rate of 99.64% with the Fe/As molar ratio of 2:1 and Ca/Fe molar ratio of 1.5:1. With both FeSO 4 +Ca(OH) 2 (FSCH) and FeSO 4 +CaCO 3 (FSCC), several analytical methods including SEM-EDS, XRD, FTIR, and TG-DSC etc. were performed to characterize the sediments. The sediment from FSCC has much larger particle size, six time faster filtration speed and only one-third volume compared with that from traditional FSCH, allowing a very easy handling of the precipitate sludge, another clear advantage of using CaCO 3. Moreover, much less fine and sticky CaSO 4 was generated in the FSCC sludge than that from FSCH. Image 10298911 • Arsenic removal dramatically improved by CaCO 3 instead of Ca(OH) 2 with FeSO 4. • The sludge after arsenic removal by CaCO 3 with FeSO 4 is easy handling. • Sludge from CaCO 3 has six time faster filtration speed than that from Ca(OH) 2. • Sludge from CaCO 3 only has one-third volume compared to that from Ca(OH) 2. [ABSTRACT FROM AUTHOR]

Abstract A simple and novel method was developed at first time to enhance As (V) removal by zero valent iron (ZVI) and activated ZVI/Fe 3 O 4 media (AIM) through air injection at intervals. Fe (II) was essential to trigger As (V) removal by ZVI and AIM, and magnetite did not improve As (V) removal. In presence of 0.5 mM Fe (II) under anaerobic condition, 10 g L−1 ZVI and AIM showed same As (V) removal efficiency including percentage, capacity and rate of >99.999%, 3.0 mg/g ZVI/AIM and 0.013 mg As (V)/(g · min), respectively. Compared to the passivation of ZVI and AIM after one-time air injection, As (V) removal efficiency was significantly improved by intermittent air injection with increased air volume and injection frequency. After third time of 1.0 mL air injection at 30 min intervals, As (V) removal percentage and capacity remained same remarkable values as that under anaerobic condition, but total removal rate was further improved to 0.033 mg As (V)/(g · min). XPS results indicated that As (V) was completely reduced to As (III) and As (0) by Fe (0) under anaerobic condition, but quick adsorption/co-precipitation of As (V) followed by reduction to As (III) and As (0) by Fe (0) was the main mechanism under aerobic condition. This study suggests the addition of Fe (II) followed by simple air injection at intervals harnesses the reactivity of traditional ZVI for arsenic removal. Graphical abstract Image 102718 Highlights • Fe (II) was essential to activate ZVI and AIM systems to remove As (V). • ZVI and AIM showed high As (V) removal percentage, capacity and rate anaerobically. • As (V) removal efficiency was significantly improved by injecting air at intervals. • As (V) removal mechanisms under aerobic and anaerobic conditions were described. [ABSTRACT FROM AUTHOR]

[Display omitted] • Ferrous can significantly elevate the stability of arsenic calcium residues (CARs). • The FeII treated CARs were more stable at neutral pH (e.g., 6 and 7) than at other pH. • Arsenic (As) deposited in the solid phase major as secondary As-bearing minerals. • XRD/TEM/XAS results confirmed the formation of ferrous arsenates in the solid phase. • The FeII treated aerobic/anoxic CARs both have high leaching stability at neutral pH. This work proposed an in-situ method for stabilizing the hazardous calcium arsenic residues (CARs) by introducing small amounts of ferrous (FeII) solution to induce the formation of stable ferrous arsenate minerals. The CARs collected from a copper smelter in China were treated with FeII solution at room temperature, FeII/As molar ratios of 0.5–2 and pH 6–9 under both oxic and anoxic conditions, and the concentrations of aqueous arsenic (As) was monitored during the whole treatment process (up to 760 days). Results showed that As dissolution was significantly inhibited after addition of FeII into the CARs slurries. The concentration of dissolved As was lowered to < 2.0 mg/L from initially ∼ 1000 mg/L at pH 6 and 7, and FeII/As ≥ 1. The resultant solids under these conditions showed TCLP As concentrations of < 1.0 mg/L, which were dramatically lower than that of untreated CARs (862 mg/L). Characterization with X-ray powder diffraction (XRD), scanning/transmission electron microscopy (SEM/TEM), and X-ray absorption spectroscopy (XAS) of the resultant solids revealed that the formation of ferrous arsenates minerals (parasymplesite and/or ferrisymplesite) was the mechanism of the stabilization effects. The FeII treatment method proposed in this work provides an alternative option for in-situ CARs stabilization. [ABSTRACT FROM AUTHOR]

[Display omitted] Highly efficient azo-day quinazolinone derivatives carrying a π bond and OH electron donor groups have been designed, synthesized, and evaluated as colorimetric chemosensors for detecting metal ions in biological and environmental samples, which was further supported by the DFT studies and UV–vis titration experiment. The 3-amino-2-styrylquinazolin-4(3H)-one (1) was directed to react with phenols during a diazotization type reaction to form a series of azo-day 3-(diazenyl)-2-(styryl)quinazolin-4(3H)-one (4a-e), which could not only have been confirmed by FTIR, H1NMR, C13NMR, Ms and elemental analysis but could also be easily used for the detection of metal ions. Compound 4c exhibited a rapid qualitative and quantitative method for the detection of CoII at λ max (582 nm) and FeII at λ max (566 nm) in an aqueous solution. The current study introduces a facile, low cost, more specific and selective chemosensor for detecting trace amounts of cobalt and ferrous ions. [ABSTRACT FROM AUTHOR]

The wide choice of materials available today has posed a major challenge for designers and engineers to select the most suitable material and manufacturing process for any engineering application. The mechanical and tribological properties have been a great concern, as the life of a product significantly depends upon these two aspects. Researchers have developed various composites with different compositions comprising of metals or metals with non metallic fillers to enhance these properties economically. Development of various Iron based antifriction composite materials is one amongst such composites as these are readily available with low cost. Sintered steels are also being used in gears and bearings due to economic and technical characteristics. Thus, new compositions with improved wear and friction properties have become a thrust area for tribologists and designers in the research world. This paper presents a review on various solid lubricants used in ferrous based compositions in order to enhance the mechanical and tribological properties.