Iron Metal Ions Research Articles

(Invited) Graphene Oxide As an Additive for Ni-Fe Electrodeposition

In contrast to graphene, graphene oxide (GO) is readily disperse in aqueous electrolytes and can be reduced along with nickel and iron metal ions. While others had incorporated graphene in Ni-Fe deposits, no previous studies have addressed the role of GO particles on metal deposition. Ni-Fe is characterized by the anomalous codeposition behavior where there is a tendency of more Fe to be deposited than Ni even though there is an excess of Ni ions in the electrolyte. This behavior has been modeled assuming adsorbed intermediates. Here, the influence of GO on the deposit composition, structure and anomalous codeposition effect is investigated. The deposits were galvanostatically electrodeposited from a boric acid-sulfamate electrolyte at pH 2 containing commercial graphene oxide platelets. Two different cell configurations were examined:1) a rotating cylinder electrode (RCE) and 2) a copper mesh. The rotating cylinder as a working electrode was used in order to investigate mass transport. The copper mesh working electrode was placed in close contact to a flat bottom pH probe in order to examine the local pH change. The addition of GO to the electrolyte had an effect on the deposit composition and the local pH change (Fig 1). The deposit composition had either more Ni or remained the same compared to an electrolyte without GO on the RCE electrode at electrode rotation rates of 372 and 1000 rpm (Fig 1 (a) and (b)). The larger Ni content in the deposit was due to an enhanced Ni partial current density in the presence of GO. The local pH during the deposition on the mesh electrode with vigorous electrolyte stirring increased the local pH (Fig 1(c)). The composition behavior is similar to the results from the RCEs, with higher Ni content in the presence of GO. The local pH increase when GO was present is considered a factor that drives the enhanced Ni content, that may be a consequence of changes in adsorbed hydrogen. GO was not incorporated into the deposit; however, it had a dramatic effect on the morphology. There was less micro-cracks when GO was present in the electrolyte suggesting less adsorbed hydrogen. Thus, GO influenced the adsorbed intermediates making the electrodeposition less anomalous and having less cracks. Acknowledgement: This work was supported in part by the AESF Foundation. Figure 1. The influence of GO in the electrolyte during Ni-Fe electrodeposition (a) composition on a RCE, rotating rate (a) 372, (b)1000 rpm and (c) local pH measurements on a mesh electrode under vigorous stirring, 30 mA/cm2. Figure 1

Development of Voltammetry Analysis Method of Iron Metal Ions by Solid-State Membrane with Carbon Nanotube

This work developed a selectively modified electrode for measuring the Fe(II) ions in continuous integration using voltammetry techniques. The study assessed various aspects, such as linearity, scan rate, repeatability, and real sample analysis. The experiment is performed using differential pulse voltammetry (DPV). The findings of the study indicated that the voltammetry method exhibited a regression line of y = 36.507 ln(x) + 990.73, with a correlation value of 0.9627, with an optimum scan rate of 20 mV/s and good repeatability over five times measurement. On the other hand, when comparing the results using the UV-Vis spectrophotometric technique, the regression equation was found to be y = 0.20438x − 0.06987, with a correlation value of 0.99583. Notably, the voltammetry measurement outperformed the UV-Vis method since it allowed analysis of Fe(II) at concentrations up to 6.35 × 10−4 ppm (or 1.00 × 10−11 M), while the UV-vis measurement could only analyze up to 1.5 ppm (or 2.36 × 10−5 M). Consequently, the developed technique proves to be superior to the other methods for the analysis of Fe(II).

Distinct mechanisms of iron and zinc metal ions on osteo-immunomodulation of silicocarnotite bioceramics

The immunomodulatory of implants have drawn more and more attention these years. However, the immunomodulatory of different elements on the same biomaterials have been rarely investigated. In this work, two widely used biosafety elements, iron and zinc added silicocarnotite (Ca5(PO4)2SiO4, CPS) were applied to explore the routine of elements on immune response. The immune reactions over time of Fe-CPS and Zn-CPS were explored at genetic level and protein level, and the effects of their immune microenvironment with different time points on osteogenesis were also investigated in depth. The results confirmed that both Fe-CPS and Zn-CPS had favorable ability to secret anti-inflammatory cytokines. The immune microenvironment of Fe-CPS and Zn-CPS also could accelerate osteogenesis and osteogenic differentiation in vitro and in vivo. In terms of mechanism, RNA-seq analysis and Western-blot experiment revealed that PI3K-Akt signaling pathway and JAK-STAT signaling pathways were activated of Fe-CPS to promote macrophage polarization from M1 to M2, and its immune microenvironment induced osteogenic differentiation through the activation of Hippo signaling pathway. In comparison, Zn-CPS inhibited polarization of M1 macrophage via the up-regulation of Rap1 signaling pathway and complement and coagulation cascade pathway, while its osteogenic differentiation related pathway of immune environment was NF-κB signaling pathway.

Elucidating the impact of sanitary waste on the formation of fat, oil and grease deposits in sewer systems

The accumulation of fat, oil and grease (FOG) deposits in sanitary sewer systems is a significant cause of sewer overflows, mainly due to their tendency to adhere to pipe walls. The aim of this study is to (i) develop laboratory-prepared FOG deposits using a mixture of iron (Fe) and aluminium (Al) metal ions, fatty acids, saccharides and cooked oils, in addition to various sanitary waste materials such as paper towels, wipes and pads and (ii) examine the characteristics of these FOG deposits. The goals of this study were to (i) gain a deeper understanding of the impact of sanitary waste on the formation of FOG deposits and (ii) discuss the detailed physiochemical properties of these FOG deposits. The findings revealed that FOG deposits can vary in nature, appearing as either a smooth, paste-like substance or a coarse, semi-solid material, depending on the types of waste present in the sewer. Analysis of the fatty acid profile indicated that the FOG deposits with wipes have the highest viscosity (3.2 × 104 Pa s) and larger composition of smaller chain saturated fatty acids (caprylic acid 0.64%, undecanoic acid 5.61%, lauric acid 4.65%, myristic acid 3.21% and palmitic 8.38%). In contrast, FOG deposits with Fe and Al metal impurities have higher heat resistance and thermal stability (melting point of 125 °C) and have larger composition of long chain fatty acids. Furthermore, FTIR analysis confirmed that these FOG deposits are composed of metallic salts of fatty acids, aligning with samples from sewer lines. Our results suggest that FOG deposit formation involves the aggregation of excess calcium, which compresses free fatty acid micelles, and a saponification reaction between the calcium aggregates and free fatty acids. This research illuminates the complex processes behind FOG deposit formation and their varied characteristics, providing valuable insights into potential strategies for preventing FOG-related sewer blockages.

Over-expression of the BnVIT-L2 gene improves the lateral root development and biofortification under iron stress

The vacuolar iron transporter (VIT) family is responsible for absorbing and storing iron ions in vacuoles. Here, the BnVIT-L2 gene from Brassica napus has been cloned for the first time and was found to be expressed in multiple tissues and organs, induced by iron stress. The BnVIT-L2 protein is located in vacuolar membranes and has the ability to bind both iron and other bivalent metal ions. Over-expression of the BnVIT-L2 gene increased lateral root number and main root length, as well as chlorophyll and iron content in transgenic Arabidopsis plants (BnVIT-L2/At) exposed to iron stress, compared to wild type Col-0. Furthermore, over-expression of this gene improved the adaptability of transgenic B. napus plants (BnVIT-L2-OE) under iron stress. The regulation of plant tolerance under iron stress by BnVIT-L2 gene may involve in the signal of reactive oxygen species (ROS), as suggested by Ribosome profiling sequencing (Ribo-seq). This study provides a reference for investigating plant growth and biofortification under iron stress through the BnVIT-L2 gene.

Spectroscopically labelled hydroxylamino-triazine (BHT) siderophores toward the quantification of iron(iii), vanadium(v) and uranium(vi) hard metal ions

The first BHT luminescent siderophore-type ligand has been prepared. Coordination of the selective ligand with hard metal ions, FeIII, VV and UVI, quenches the emitted light permitting the quantification of metal ions at nM concentrations.

Quantification of Macrophage Cellular Ferrous Iron (Fe2+) Content Using a Highly Specific Fluorescent Probe in a Plate Reader.

Macrophages are at the center of innate immunity and iron metabolism. In the case of an infection, macrophages adapt their cellular iron metabolism to deprive iron from invading bacteria to combat intracellular bacterial proliferation. A concise evaluation of the cellular iron content upon an infection with bacterial pathogens and diverse cellular stimuli is necessary to identify underlying mechanisms concerning iron homeostasis in macrophages. For the characterization of cellular iron levels during infection, we established an in vitro infection model where the murine macrophage cell line J774A.1 is infected with Salmonella enterica serovar Typhimurium (S.tm), the mouse counterpart to S. enterica serovar Typhi, under normal and iron-overload conditions using ferric chloride (FeCl3) treatment. To evaluate the effect of infection and iron stimulation on cellular iron levels, the macrophages are stained with FerroOrange. This fluorescent probe specifically detects Fe2+ ions and its fluorescence can be quantified photometrically in a plate reader. Importantly, FerroOrange fluorescence does not increase with chelated iron or other bivalent metal ions. In this protocol, we present a simple and reliable method to quantify cellular Fe2+ levels in cultured macrophages by applying a highly specific fluorescence probe (FerroOrange) in a TECAN Spark microplate reader. Compared to already established techniques, our protocol allows assessing cellular iron levels in innate immune cells without the use of radioactive iron isotopes or extensive sample preparation, exposing the cells to stress. Key features • Easy quantification of Fe2+ in cultured macrophages with a fluorescent probe. • Analysis of iron in living cells without the need for fixation. • Performed on a plate reader capable of 540 nm excitation and 585 nm emission by trained employees for handling biosafety level 2 bacteria.

Construction of multiple crosslinked networks for the preparation of high-performance lignin-containing cellulose nanofiber reinforced polyvinyl alcohol films

Polyvinyl alcohol (PVA) film, a promising alternative to non-biodegradable plastic packaging films for food and medical packaging, is limited by poor water resistance. In this work, a simple solvent evaporation self-assembly was used to construct a nanophase separation structure to establish dense interfacial hydrogen bonding, covalent bonding and iron metal ion coordination interactions between lignin-containing cellulose nanofibers (LCNFs) and PVA matrix to improve the interfacial force and solve the problem of poor compatibility of LCNFs in PVA. The iron ion (Fe3+) coordination tended to combine with the more active lignin phenolic hydroxyl group to construct the nanophase separation structure. Covalent crosslinking of glutaraldehyde (GA) improved the interfacial compatibility of PVA/LCNF films, enhanced the interfacial bonding and formed a homogeneous structure. The multi-nanophase structures improved the strength and elastic modulus of the PVA/LCNF film and provided the films with extremely low water absorption, water vapor transmission rate and excellent UV-shielding. Compared with pure PVA film, PVA-10L-5Fe-3GA film had about 106.9 % higher tensile strength, 93.9 % lower water absorption and 93.4 % lower mass loss, 69.8 % lower water vapor transmission coefficient, and was able to shield UV at 200–400 nm, which is highly expected to be used in packaging films.

The chemical profiling and identification of Abelia macrotera (Graebn. et Buchw.) Rehd. based on UHPLC-Q-Exactive Orbitrap MS and study their antioxidant, anti-tyrosinase and anti-inflammatory activities

Although Abelia macrotera has long been used as the raw material for the special snack “immortal tofu” by Chinese population, the composition and activity of its leaf and stem are rarely studied. Ultrahigh-performance liquid chromatography-quadrupole (UHPLC-Q)-Exactive Orbitrap mass spectrometry and various experiments were used for in vitro study of its chemical composition and antioxidant, antityrosinase, and anti-inflammatory activities. A fast, accurate, and sensitive UHPLC-Q-Exactive Orbitrap mass spectrometry method has been established and effectively used for the determination of the chemical composition of the leaf and stem of A. macrotera. The biological activities of the leaf and stem extracts of the A. macrotera were determined in vitro by antioxidant and anti-inflammatory methods. A total of 142 chemical constituents including 48 flavonoids, 65 organic acids, 12 phenylpropanoids, and 19 others were identified by UHPLC-Q-Exactive Orbitrap mass spectrometry. The results show that the leaf and stem extracts have wide and significant antioxidant capacities, including scavenging effects of DPPH, ABTS and hydroxyl radicals, and the ability to reduce both iron and copper metal ions. Additionally, they showed a strong inhibition of NO production, with a dose-dependent inhibition. To the best of our knowledge, this is the first study to report the identification and content determination of the chemical components of the A. macrotera leaf and stem. These results will be beneficial to further understand its medicinal value.

Metal–Curcumin Complexes in Modern Pharmacotherapeutics: A Comprehensive Review

The major ingredient in turmeric, curcumin, has drawn a lot of interest as a plant-based substance having pharmacological benefits that are pleiotropic. It has immunomodulatory, neuroprotective, antibacterial, anti-inflammatory, antioxidant, hypoglycemic, and anti-inflammatory properties. Curcumin has certain health-promoting properties, but they are limited by its hydrophobicity, insolubility in water, low bioavailability, quick metabolism, and systemic elimination. Complexes of metals with curcumin have been created as a result of this unique step. The -diketone moiety of curcumin often interacts with metals to form metal-curcumin complexes. It is generally known that the metal ions of boron, cobalt, copper, gallium, gadolinium, gold, lanthanum, manganese, nickel, iron, palladium, platinum, ruthenium, silver, vanadium, and zinc are all highly chelated by curcumin. Metal-curcumin complexes’ pharmacological, chemo-preventive, and therapeutic properties are described in this paper. Metal-curcumin complexes boost the antioxidant, anti-inflammatory, antibacterial, and antiviral properties of curcumin by increasing its solubility, cellular absorption, and bioavailability. Additionally, metal-curcumin complexes have shown effectiveness against a number of chronic illnesses, such as cancer, rheumatoid arthritis, osteoporosis, and neurological conditions including Alzheimer’s disease. The regulation of inflammatory mediators, transcription factors, protein kinases, antiapoptotic proteins, lipid peroxidation, and antioxidant enzymes was linked to these biological activities of metal-curcumin complexes. Metal-curcumin complexes have also proven beneficial in radio-imaging and biological imaging. Future applications of metal-curcumin complexes might signal a fresh strategy for the management of chronic illnesses.

MsYSL6, A Metal Transporter Gene of Alfalfa, Increases Iron Accumulation and Benefits Cadmium Resistance.

Iron (Fe) is necessary for plant growth and development. The mechanism of uptake and translocation in Cadmium (Cd) is similar to iron, which shares iron transporters. Yellow stripe-like transporter (YSL) plays a pivotal role in transporting iron and other metal ions in plants. In this study, MsYSL6 and its promoter were cloned from leguminous forage alfalfa. The transient expression of MsYSL6-GFP indicated that MsYSL6 was localized to the plasma membrane and cytoplasm. The expression of MsYSL6 was induced in alfalfa by iron deficiency and Cd stress, which was further proved by GUS activity driven by the MsYSL6 promoter. To further identify the function of MsYSL6, it was heterologously overexpressed in tobacco. MsYSL6-overexpressed tobacco showed better growth and less oxidative damage than WT under Cd stress. MsYSL6 overexpression elevated Fe and Cd contents and induced a relatively high Fe translocation rate in tobacco under Cd stress. The results suggest that MsYSL6 might have a dual function in the absorption of Fe and Cd, playing a role in the competitive absorption between Fe and Cd. MsYSL6 might be a regulatory factor in plants to counter Cd stress. This study provides a novel gene for application in heavy metal enrichment or phytoremediation and new insights into plant tolerance to toxic metals.

The resin-supported iron-copper bimetallic composite as highly active heterogeneous Fenton-like catalysts for degradation of gaseous toluene.

In this study, a resin-supported iron-copper bimetallic heterogeneous Fenton catalyst with excellent removal performance, superior economy and outstanding recoverability was synthesized by an impregnation method and used to remove gaseous toluene. Experiments disclosed that 3-FeCu@LXQ-10 possessed extremely high catalytic capacity. At a temperature of 30 °C, an initial toluene concentration of 200 mg/m3 and H2O2 atomization amount of 3 mmol/h, the toluene removal efficiency of 3-FeCu@LXQ-10 was 97.50%. Experimental tests had revealed that the bimetallic supported catalysts exhibited higher catalytic activity than single metal-supported catalysts, owing to an interaction effect between iron and copper metal ions. Furthermore, electron paramagnetic resonance (EPR) and radical quenching tests were carried out, and the results indicated •OH radicals performed a key role in the Fenton-like process. In addition, the iron-copper bimetallic catalysts exhibited good reusability and stability characteristics during six degradation cycles. This study shows promising potential in using FeCu@LXQ-10 as a heterogeneous catalyst for removing toluene.

Improving yields by switching central metal ions in porphyrazine-catalyzed oxidation of glucose into value-added organic acids with SnO2 in aqueous solution.

Photocatalysis has exhibited huge potential in selective conversion of glucose into value-added chemicals. Therefore, modulation of photocatalytic material for selective upgrading of glucose is significant. Here, we have investigated the insertion of different central metal ions, Fe, Co, Mn, and Zn, into porphyrazine loading with SnO2 for access to more efficient transformation of glucose into value-added organic acids in aqueous solution at mild reaction conditions. The best selectivity for organic acids containing glucaric acid, gluconic acid, and formic acid of 85.9% at 41.2% glucose conversion was attained by using the SnO2/CoPz composite after reacting for 3h. The effects of central metal ions on surficial potential and related possible factors have been studied. Experimental results showed that the introduction of metalloporphyrazine with different central metal ions on the surface of SnO2 has a significant effect on the separation of photogenerated charges, changing the adsorption and desorption of glucose and products on the catalyst surface. The central metal ions of cobalt and iron contributed more to the positive effects toward enhancing conversion of glucose and yields of products, and manganese and zinc contributed more to the negative effects, resulting in the poor yield of products. The differences from the central metals may attribute to the surficial potential change of the composite and the coordination effects between the metal and oxygen atom. An appropriate surficial potential environment of the photocatalyst may achieve a better interactive relationship between the catalyst and reactant, while appropriate ability of producing active species matched with adsorption and desorption abilities would gain a better yield of products. These results have provided valued ideas for designing more efficient photocatalysts in selective oxidation of glucose utilizing clean solar energy in the future.

A review on the inference of doping TiO2 with metals/non-metals to improve its photocatalytic activities

The band-gap energy of TiO2 nanoparticles has been modified using different methods. The study reviewed the effects of doping and co-doing TiO2 nanotubes with different metals and nonmetals to modify its band gap and improves the photocatalytic activity of the nanoparticles. From our findings reviewing different articles, co-doing TiO2 using dissimilar metal ions like Cerium (Ce) together with nitrogen (N) ions or chromium (Cr) and iron (Fe) ions will decrease particle size, broaden the area of the surface, and as well modifies the particle’s band-gap for visible light to energize an electron causing its movement from the valance band to the conduction band. The studies also revealed that co-doping TiO2 with chromium and iron metal ion demonstrated twice the photocatalytic activity for photodecomposition of gaseous-isopropyl alcohol when compared with single (Cr/Fe) doped TiO2 nanoparticles when exposed to visible light. The reviewed work estimated the optimal amount of Ce for Ce/N co-doped TiO2 at 0.05 grams. Different works of literature reviewed show that doping TiO2 with different transition metals reduces the band-gap for easy absorption of visible light and improvement in the photocatalytic activities of the nanoparticles.

Uso de biosorbente de coco verde para la eliminación de Hierro y Manganeso en agua de pozo

The presence of iron and manganese ions in the well water end up generating problems in the water quality that compromise its domestic and industrial use. To avoid this, it is common to use expensive technologies that end up not being as efficient as they should be. This study presents an alternative mean by using natural biosorbent materials that, in addition to presenting a great efficiency in the removal of ions from their high levels of organic matter, such as cellulose, hemicellulose and lignin, also have a high adsorption capacity due to the presence of functional groups in their structure. The research focuses on the efficiency of green coconut shells in the removal of iron and manganese metal ions present in well water collected at the Polo de Inovação do IFF. For this, analyses were performed to determine the concentration of these metals by the Atomic Absorption Method in the input samples and in the samples after the passage through the filter containing the biosorbent. The concentration in the retention of iron and manganese ions was high, 87.85% and 66.81% respectively, for the 2.0 mm granulometry of the biosorbent material.

Novel Enrofloxacin Schiff Base Metal Complexes: Synthesis, Spectroscopic Characterization, Computational Simulation and Antimicrobial Investigation against Some Food and Phyto-Pathogens

Condensation of the reaction between enrofloxacin and ethylenediamine in the existence of glacial acetic acid produced a new N,N-ethylene (bis 1-cyclopropyl-7-(4-ethylpiperazin-1-yl)-6-fluoro-1,4-dihydroquinoline-3-carboxylic acid Schiff base (H2Erx-en). H2Erx-en was used as a tetra-dentate ligand to produce novel complexes by interacting with metal ions iron(III), yttrium(III), zirconium(IV), and lanthanum(III). The synthetic H2Erx-en and its chelates had been detected with elemental analysis, spectroscopic methods, mass spectrometry, thermal studies, conductometric and magnetic measurements experiments. The calculated molar conductance of the complexes in 1 × 10−3 M DMF solution shows that iron(III), yttrium(III) and lanthanum(III) are 1:1 electrolytes, however the zirconium(IV) complex is non-electrolyte. The infrared spectra of H2Erx-en chelates indicated that the carboxylic group is deprotonated and H2Erx-en is associated with metals as a tetra-dentate through nitrogen and oxygen atoms. The disappearance of the carboxylic proton in all complexes corroborated information concerning H2Erx-en deprotonation and complexation with metal ions, according to 1H NMR data. Thermal analysis revealed the abundance of H2O particles in the chelates’ entrance and outlet spheres, indicating the disintegration pattern of H2Erx-en and their chelates. The Coats–Redfern and Horowitz–Metzeger approaches were utilized to calculate the thermodynamic items (Ea, ΔS *, ΔH *, and ΔG *) at n = 1 and n ≠ 1. The resulting data reveal better organized chelate building activation. Density functional theory (DFT) was created to properly grasp the optimal architecture of the molecules. The chelates are softer than H2Erx-en, with estimates varying between 95.23 eV to 400.00 eV, compared to 31.47 eV for H2Erx-en. The disc diffusion technique was utilized to assess H2Erx-en and their chelates in an antimicrobial assay against various food and phytopathogens. The zirconium(IV) chelate has the most potent antibacterial action and is particularly efficient against Salmonella typhi.

The Key Element Role of Metallophores in the Pathogenicity and Virulence of Staphylococcus aureus: A Review.

Simple SummaryMetallophores, which are secondary metabolites secreted by bacteria, play an important role in their virulence. The bacterium Staphylococcus aureus produces several types of metallophores, such as staphyloferrin A, staphyloferrin B, and staphylopine, which are responsible for metal ion sequestering. The former is specific for iron chelating, while the latter is a wide-spectrum metallophore, but it mainly chelates zinc. The detailed description of the biosynthesis, export and import processes of each metallophore type is highlighted in this review. Moreover, the genetic regulation is explained as well. Previous studies that provide evidence about the crucial part of metallophores in Staphylococcus aureus pathogenesis were also mentioned herein.The ubiquitous bacterium Staphylococcus aureus causes many diseases that sometimes can be fatal due to its high pathogenicity. The latter is caused by the ability of this pathogen to secrete secondary metabolites, enabling it to colonize inside the host causing infection through various processes. Metallophores are secondary metabolites that enable bacteria to sequester metal ions from the surrounding environment since the availability of metal ions is crucial for bacterial metabolism and virulence. The uptake of iron and other metal ions such as nickel and zinc is one of these essential mechanisms that gives this germ its virulence properties and allow it to overcome the host immune system. Additionally, extensive interactions occur between this pathogen and other bacteria as they compete for resources. Staphylococcus aureus has high-affinity metal import pathways including metal ions acquisition, recruitment and metal–chelate complex import. These characteristics give this bacterium the ability to intake metallophores synthesized by other bacteria, thus enabling it to compete with other microorganisms for the limited nutrients. In scarce host conditions, free metal ions are extremely low because they are confined to storage and metabolic molecules, so metal ions are sequestered by metallophores produced by this bacterium. Both siderophores (iron chelating molecules) and staphylopine (wide- spectrum metallophore) are secreted by Staphylococcus aureus giving it infectious properties. The genetic regulation of the synthesis and export together with the import of metal loaded metallophores are well established and are all covered in this review.

Applications of Plants Leaf-Based Biosorbents for Removal of Iron and Phosphorus from Contaminated Water: A Review

The pure water contains 3% in the global. Human and manufacturing performances create and release wastes having iron and phosphorous metals into the water assets production them polluted and dangerous human health and environment. The usual processes for the elimination of iron and phosphorous metal ions those by chemical precipitation and membrane filtration are very costly while purifying huge concentrations of water, ineffective at lower amounts of metal and produce huge amount of sludge and other poisonous materials that need suspicious dumping. Bio-sorption is ecological and alternatives processes for purification of waste water. These events have positive remuneration on the most excellent processes suitable it include a lesser price, simply obtainable and reused. The procedure can be prepared cheaply by recycling and reusing the bio-sorbent following eliminating the poisonous metal. Biosorption is influenced by the various type’s parameters those are pH, temperature, initial metal ion concentration, biosorbent concentration and rate of mixing. The different bioreactors can be applied in biosorption for the elimination of metal ions from huge concentration of water. In this manuscript we are discussed about the preparation of various types of biosorbents for elimination of iron and phosphorous from contaminated water.

Economic and fast electro-flotation extraction of heavy metals from wastewater

ABSTRACT Fast electroflotation extraction of heavy metals from wastewater is described. The results of experimental investigations of the extraction of iron, aluminium and chromium hydroxides from aqueous solutions in the presence of surfactants of various natures and ions of calcium by electroflotation are presented. It was found that the presence of Ca2+ in the solution at a concentration of 0.5 g/L reduced the degree of electroflotation extraction of Al(OH)3, Fe(OH)3, Cr(OH)3 regardless of the nature of the electrolyte. The addition of surfactants in the system in the presence of Ca2+ increased the amount of extraction of the dispersed phase. The greatest effect is achieved with the help of anionic surfactant sodium dodecyl sulphate, while the degree of extraction reached 98%. The high efficiency of the process of electroflotation extraction of the dispersed phase was due to the hydrophobization of the particle surface owing to the adsorption of surfactants on the surface of hydroxides. The recent method is useful to treat wastewater contaminated with aluminium, iron and chromium metal ions. The reason is that this method is very fast working within 20 min; Moreover, pH 7.0 working made this method ideal for utilisation in natural water treatment economically.

A Synergistic Effect of Phthalimide-Substituted Sulfanyl Porphyrazines and Carbon Nanotubes to Improve the Electrocatalytic Detection of Hydrogen Peroxide.

A sulfanyl porphyrazine derivative with peripheral phthalimide moieties was metallated with cobalt(II) and iron(II) metal ions. The purity of the macrocycles was confirmed by HPLC, and subsequently, compounds were characterized using various analytical methods (ES-TOF, MALDI-TOF, UV–VIS, and NMR spectroscopy). To obtain hybrid electroactive electrode materials, novel porphyrazines were combined with multiwalled carbon nanotubes. The electrocatalytic effect derived from cobalt(II) and iron(II) cations was evaluated. As a result, a significant decrease in the overpotential was observed compared with that obtained with bare glassy carbon (GC) or glassy carbon electrode/carbon nanotubes (GC/MWCNTs), which allowed for sensitive determination of hydrogen peroxide in neutral conditions (pH 7.4). The prepared sensor enables a linear response to H2O2 concentrations of 1–90 µM. A low detection limit of 0.18 μM and a high sensitivity of 640 μA mM−1 cm−2 were obtained. These results indicate that the obtained sensors could potentially be applied in biomedical and environmental fields.