Phosphate Complexes Research Articles

Biomimetic non-collagenous proteins-calcium phosphate complex with superior osteogenesis via regulating macrophage IL-27 secretion

Traumatic defects or non-union fractures presents a substantial challenge in the fields of tissue engineering and regenerative medicine. Although synthetic calcium phosphate-based biomaterials (CaPs) such as dibasic calcium phosphate anhydrate (DCPA) are commonly employed for bone repair, their inadequate cellular immune responses significantly impede sustained degradation and optimal osteogenesis. In this study, drawing inspiration from the key structure of an acidic non-collagenous protein-CaP complex (ANCPs-CaP) essential for natural bone formation, we prepared biomimetic mineralized dibasic calcium phosphate (MDCPA). This preparation utilized plant-derived non-collagenous protein Zein as the organic template and acidic artificial saliva as the mineralization medium. Physicochemical property analysis revealed that MDCPA is a complex of Zein and DCPA, which mimics the composite of the natural ANCP-CaP. Moreover, MDCPA exhibited enhanced biodegradability and osteogenic potential. Mechanistic insight revealed that MDCPA can be phagocytized and degraded by macrophages via the FCγRIII receptor, leading to the release of interleukin 27 (IL-27), which promotes osteogenic differentiation by osteoimmunomodulation. The critical role of IL-27 in osteogenesis is further confirmed using IL-27 gene knockout mice. Additionally, MDCPA demonstrates effective healing of critical-sized defects in rat cranial bones within only 4 w, providing a promising basis and valuable insights for critical-sized bone defects regeneration.

Phosphate ligand-mediated production of reactive oxygen species during oxygenation of Fe(II)-phosphate complexes

Reactive oxygen species (ROS) production upon the oxygenation of reduced iron minerals is of critical importance to redox cycles of Fe and the fate of refractory organic contaminants. The environmental impact factors during this process, however, have been underappreciated. In this study, prominently enhanced production of hydroxyl radicals (•OH) was observed by oxygenation of Fe(II) with 5–50 mM phosphate. The results of spin trap electron spin resonance (ESR) experiment showed that Fe(II)-phosphate complexes facilitated the generation of •OH. The degradation experiment of p-nitrophenol (PNP) confirmed that •OH formation was dominated by a consecutive one-electron O2 reduction (90.2–96.9 %), and the quantification of PNP degradation products revealed that Fe(II)/phosphate molar ratios regulated the O2 activation pathways for O2•− or •OH production. The further experimental and theoretical investigation demonstrated that the coordination of phosphate with Fe(II) plays a dual role in ROS generation that facilitated O2•− formation by lowering the energy barrier for Fe(II) oxidation and altered the reaction pathway of •OH formation due to its occupation of sites for electron transfer. The present work highlights an important role of natural oxyanions in O2 activation by Fe(II) and raises the possibility of in situ degradation of contaminants in subsurface environment.

Highly selective and efficient Pb2+ capture using PO4-loaded 3D-NiFe layer double hydroxides derived from MIL-88A

Lead (Pb) contamination in water requires improved decontamination technologies. The addition of phosphate to precipitate Pb2+ is a widely used method for remediating Pb in soil and water, though it has certain limitations. This study focuses on novel 3D mesoporous layered double hydroxide (LDH) sorbents functionalized with phosphate anions for Pb2+ removal from contaminated waters. Our innovative strategy involves converting a sacrificial template metal-organic frameworks (MOFs) structure (MIL-88A(Fe)) into NixFe LDH, followed by an anion exchange reaction with phosphate anions. This process preserves the 3D microrod architecture of MIL-88A and prevents deleterious LDH particle aggregation. The synthesis results in stable microrod crystals, 1–2 μm long, composed of 3D assemblies of NixFe-PO4 LDH nanoplatelets with a specific surface area exceeding 110 m2/g. The novel LDH materials display fast adsorption kinetics (pseudo-second order model) and remarkably high Pb2+ removal performances (Langmuir isotherm model) with a capacity of 538 mg/g, surpassing other reported adsorbents. LDH-PO4 exhibits high selectivity for Pb2+ over competing ions like Ni2+ and Cd2+ (selectivity order is: Pb2+ > Ni2+ > Cd2+). Removal of Pb2+ from NixFeLDH/88A-PO4 involves various mechanisms, including surface complexation and surface precipitation of lead phosphate or lead hydroxide phases as revealed by structural characterization techniques.

Hydrothermal mineral replacement in the apatite-rhabdophane-monazite system: Experiments, reaction mechanisms and geological implications

Apatite, rhabdophane and monazite are actinide- and rare-earth element (REE)-bearing phosphate minerals with diverse geoscientific applications. However, their mineral-fluid reaction mechanisms below 200 °C are understudied. Insufficient understanding as to how these minerals behave during hydrothermal alteration impedes useful interpretations of REE-U-Th mobilisation in regolith profiles, diagenetic environments and low-temperature hydrothermal systems. This work experimentally investigates the replacement of apatite by rhabdophane in a Ce-doped acidic fluid at 30 °C, and of rhabdophane by monazite in REE-barren acidic fluids at 180 °C. Rhabdophane replaced apatite via the coupled dissolution-precipitation mechanism, forming nanoscale prisms clustered into spherulitic aggregates. Interstitial voids that formed between rhabdophane and apatite indicate how rhabdophane precipitation was the rate-limiting step. Void widths varied in response to apatite's anisotropic dissolution; rapid dissolution parallel to the c-axis formed the widest voids (50–125 μm) and thickest rhabdophane layers (20–50 μm), while slow dissolution perpendicular to the c-axis formed narrower voids (< 1 μm) and thinner layers (< 5 μm). At 180 °C, monazite also replaced rhabdophane via the dissolution-precipitation mechanism. Replacement rates increased with increasing phosphate concentrations, implying that monazite precipitation was the rate-limiting step. However, microscale rhabdophane aggregates were pseudomorphically preserved. This is attributed to the shared orientation of rhabdophane prisms (not pseudomorphically preserved) and their intergranular boundaries which, as microreactors, guided monazite precipitation. Both replacement reactions were accompanied by a loss of U to solution, which is attributed to the stabilisation of uranyl-phosphate complexes under acidic conditions. Results indicate that: 1) anisotropic dissolution can govern the extent of rate coupling between dissolution and precipitation during mineral replacement; 2) the pseudomorphic replacement of mineral aggregates can occur when precipitation is the rate-limiting step; 3) rhabdophane is a feasible (and perhaps necessary) metastable precursor to authigenic monazite precipitation in low temperature hydrothermal systems; 4) highly porous aggregates of both rhabdophane and monazite generate insufficient EPMA totals, such that they cannot be differentiated by EPMA alone, and; 5) phosphate complexes can mobilise U under certain hydrothermal conditions, with implications for geochronology, nuclear waste management and the formation of REE deposits.

Microwave-assisted hydrothermal synthesis of carbonated apatite with calcium and phosphate resources derived from green mussel shell and bovine bone wastes

Resources recovery of calcium and phosphates from respective green mussel shells and bovine bones by calcination and chemically extracting are viable precursors for carbonate-rich apatite biomedical material applications. Because of their high osteoconductivity, carbonate-rich apatite bioceramics are being studied intensively for synthetic bone transplants. In the study, powder processing routes of calcination and following chemical dissolution in MgCl2 and H2SO4 were each for recovering calcium of mussel shells and phosphate of bovine bones yielding a crystal-forming solution feedstock for use in microwave-irradiated synthesis. FTIR spectra and XRD patterns validated the crystallinity and phase identification for as-synthesized powders. As a result, the presence of CO3, PO43-, and OH- bands in carbonate-calcium phosphate complexes were present in FTIR spectra. According to the XRD Rietveld method, the as-synthesized powder product contained brushite, carbonated hydroxyapatite (CHA), calcite, and gypsum. The recoverable CHA crystallites' size was 40 nm. This present study demonstrated that microwave irradiation synthesis of CHA powder with calcium and phosphates derived from mussel shells and bovine bones is the potential to yield a large amount of CHA for bioceramics and would aid in the design of a powder processing step for preparing the CHA powder precursor in biomedical applications.

Divalent metal ion in the active site of purple acid phosphatase modulates substrate binding: Kinetic and thermodynamic properties

The purple acid phosphatase was purified from 5.9-fold to apparent homogeneity from Anagelis arvensis seeds using SP-Sephadex C-50 and Sephadex G-100 chromatography. The results of residual activity tests conducted using different temperature ranges (50–70 °C) were calculated as the activation energy (Ed = 72 kJ/mol), enthalpy (69.31 ≤ (ΔH° ≤ 69.10 kJ/mol), entropy (−122.48 ≤ ΔS° ≤ −121.13 J/mol·K), and Gibbs free energy (108.87 ≤ ΔG° ≤ 111.25 kJ/mol) of the enzyme irreversible denaturation. These thermodynamic parameters indicate that this novel PAP is highly thermostable and may be significant for use in industrial applications. However, it may be confirmed by stopped-flow measurements that this substitution produces a chromophoric Fe3+ site and a Pi-substrate interaction that is about ten times faster. Additionally, these data show that phenyl phosphate hydrolysis proceeds more rapidly in metal form of A. arvensis PAP than the creation of a μ-1,3 phosphate complex. The Fe3+ site in the native Fe3+-Mn2+ derivative interacts with it at a faster rate than in the Fe3+-Fe2+ form. This is most likely caused by a network of hydrogen bonds between the first and second coordination spheres. This suggests that the choice of metal ions plays a significant role in regulating the activity of this enzyme.

Determination of insoluble (INSOL) calcium content in Cheddar, Feta, Juustoleipa, and Mozzarella cheeses using acid-base buffering curves

The amount of colloidal calcium phosphate (CCP) complex associated with caseins (INSOL Ca) determines the body, texture, flavor and breakdown of cheese constituents during aging. The continuous pH decline during cheese making because of lactic acid fermentation results in solubilization of insoluble (INSOL) calcium. Measuring INSOL Ca in such a dynamic and wide range pH system (6.6 to 5.3) is challenging. The purpose of this study was to test utility of acid-base auto-titration method in differentiating INSOL Ca content in cheeses with a wide range of pH (i.e., Juustoleipa 6.6, Mozzarella 5.6, Cheddar 5.3, Feta 4.8) and also to understand the relationship between pH, protein content, and INSOL Ca. A positive relationship was obtained for pH (R2 = 0.62) and protein content (R2 = 0.85) with INSOL Ca, suggesting concomitant release of CCP content at lower pH values and association of higher amount of CCP with higher protein content. Despite having a pH slightly closer to Mozzarella (pH 5.56), Cheddar cheese (pH 5.25) had more INSOL Ca (0.67%) owing to the highest amount of protein (26%) and low moisture content (33%). Feta had the lowest amount of INSOL Ca (0.15%) owing to a low pH (4.79), higher moisture content (55%), and low protein content (14%). Juustoleipa had the highest percentage of INSOL Ca out of total calcium (88%) due to higher pH (6.62) and more intact casein. It was evident that the acid-base titration method was able to differentiate INSOL Ca between different types of cheeses with varying pH and protein content. Findings of this work will help tracking the proportion of INSOL Ca at various stages of cheese making and understanding kinetics of INSOL Ca solubilization and its role in causing pH variation in the early stage of cheese ripening.

Uranium enrichment driven by paleomarine condition and event deposition: Insights from the lower Cambrian Niutitang Formation organic-rich shales in northeastern Guizhou, South China

Organic-rich shale related uranium (U) mineralization has attracted widespread attention as a strategic and clean alternative to fossil energy and a paleoceanic redox proxy. A comprehensive study of mineralogy, organic geochemistry and elemental geochemistry of the lower Cambrian Niutitang Formation organic-rich shales in northeastern Guizhou, South China was conducted to address this issue. SEM-EDS results showed that the U occurrence state in the Niutitang Formation shales is dominated by nanoscale U minerals, mainly including coffinite, brannerite, U-bearing apatite and U-bearing xenotime. Various states of U are closely associated with organic matter, apatite, pyrite and clay minerals. Based on geochemical indexes, paleomarine condition and event deposition jointly drove the U enrichment in the Niutitang shales, in which hydrothermal activities and/or volcanic eruptions increased U fluxes in seawater and euxinic environment with high primary productivity provided a favorable condition for U reduction. The adsorption, complexation and reduction of UO22+ by organic matter and the formation of uranyl phosphate complexes by the combination of phosphate and UO22+ accelerated U immobilization and enrichment from bottom water to sediments. The microbial activities (e.g., BSR) in this process created favorable euxinic conditions and released inorganic-phase P to provide available ligands for UO22+. The U enrichment models of the lower Cambrian Niutitang shales in northeastern Guizhou were established. This paper provides a new insight into the U enrichment mechanism in organic-rich shales, and may also have implications for the applicability of U as redox proxy and the exploration of organic-rich shale related U deposits.

In-situ detection of Pb2+ based on the ternary dihydrogen phosphate complex by surface-enhanced Raman scattering

Surface-enhanced Raman scattering (SERS) is a convenient and fast technique to detect toxic heavy metals such as lead ions (Pb2+). In this study, a silver nanoparticle-decorated hydrogel substrate by a one-pot method is prepared, addressing the instability of traditional sol substrates and the non-tunability of localized surface plasmon resonance (LSPR) of solid substrates, which can achieve in-situ detection of Pb2+ in real systems using a portable Raman spectrometer. Meanwhile, the characteristic SERS peaks attributed to the ternary complex of 4-MBA/H2PO4-/Pb2+ formed by the dihydrogen phosphate, 4-mercaptobenzoic acid, and Pb2+ are used firstly for Pb2+ detection to our knowledge, decreasing the cost of the classical strategy. The method is highly anti-interference, simple, and cost-effective, which exhibits a good linear correlation (y= 21.6x + 2711, R2=0.993) in the range of 3–500 μg/L with a detection limit of 1.6 μg/L that is one order of magnitude lower than that of the EPA regulations. This method is expected to realize the rapid and accurate on-site SERS detection of Pb2+ by the new strategy.

Investigation of the properties of alumophosphate solutions and products crystallized from them

The physicochemical properties of freshly prepared alumophosphate solutions obtained in the Al(OH)3 – H3PO4 – H2O system with the molar ratio n(Al2O3) : n(P2O5) = 1.0 : 2.75 have been investigated. The density and temperature dependence of the dynamic viscosity of the studied solutions with a concentration of P2O5 300–485 g/l were studied. The values of the apparent activation energy of the viscous flow (Eη) of alumophosphate solutions are calculated and the concentration range (390–420 g/l P2O5) is established, in which Eη is practically constant and is 15.0 kJ/mol. It is suggested that the change in the activation energy of the viscous flow of alumophosphate solutions is due to their structure determined by the composition of aluminum phosphate complexes. The influence of the viscosity properties of alumophosphate solutions and their concentration on the crystallization process of hydrated alumophosphate, in particular, the duration of the induction period and the rate of phase formation, is shown.

In-Depth Analysis of the Species and Transformations during Sol Gel-Assisted V2PC Synthesis.

The sol-gel reaction mechanism of 211 MAX phases has proven to be very complex when identifying the intermediate species, chemical processes, and conversions that occur from a mixture of metal salts and gelling agent into a crystalline ternary carbide. With mostly qualitative results in the literature (Cr2GaC, Cr2GeC, and V2GeC), additional analytical techniques, including thermal analysis, powder diffraction, total scattering, and various spectroscopic methods, are necessary to unravel the identity of the chemical compounds and transformations during the reaction. Here, we demonstrate the combination of these techniques to understand the details of the sol-gel synthesis of MAX phase V2PC. The metal phosphate complexes, as well as amorphous/nanocrystalline vanadium phosphate species (V in different oxidation states), are identified at all stages of the reaction and a full schematic of the reaction process is suggested. The early amorphous vanadium species undergo multiple changes of oxidation states while organic species decompose releasing a variety of small molecule gases. Amorphous oxides, analogous to [NH4][VO2][HPO4], V2PO4O, and VO2P2O7 are identified in the dried gel obtained during the early stages of the heating process (300 and 600 °C), respectively. They are carbothermally reduced starting at 900 °C and subsequently react to crystalline V2PC with the excess carbon in the reaction mixture. Through CHN analysis, we obtain an estimate of left-over amorphous carbon in the product which will guide future efforts of minimizing the amount of carbon in sol gel-produced MAX phases which is important for subsequent property studies.

Modeling of phosphate speciation on goethite surface: Effects of humic acid

Iron (hydr)oxides and humic acid (HA) are important active components in soils and usually coexist in the environment. The effects of HA on the adsorption and subsequent immobilization of phosphate on iron (hydr)oxide surface are of great importance in studies of soil fertility and eutrophication. In this study, two types of goethite with different particle sizes were prepared to investigate the phosphate adsorption behaviors and complexation mechanisms in the absence or presence of HA by combining multiple characterization and modeling studies. The adsorption capacity of micro- (M-Goe) and nano-sized goethite (N-Goe) for phosphate was 2.02 and 2.04 μmol/m2, which decreased by ∼25% and ∼45% in the presence of 100 and 200 mg/L HA, respectively. Moreover, an increase in equilibrium phosphate concentration significantly decreased the adsorption amount of goethite for HA. Charge distribution-multisite surface complexation (CD-MUSIC) and natural organic matter-charge distribution (NOM-CD) modeling identified five phosphate complexes and their corresponding affinity constants (logKP). Among these phosphate complexes, FeOPO2OH, (FeO)2PO2, and (FeO)2POOH species were predominant complexes on the surface of both M-Goe and N-Goe across a wide range of pH and initial phosphate concentrations. The presence of HA had little effect on the coordination mode and logKP of phosphate on goethite surface. These results and the obtained model parameters shed new lights on the interfacial reactivity of phosphate at the goethite-water interface in the presence of HA, and may facilitate further prediction of the environmental fate of phosphate in soils and sediments.

Effect of partial substitution of complex phosphates with sodium bicarbonate on aggregation, conformation and gel properties of beef-pork-chicken complex myofibrillar proteins.

Complex phosphates (CP) can improve the physicochemical properties and gelation properties of myofibrillar fibrous protein (MP) in mixed meat products, but an excessive intake of phosphates over a long period of time is harmful to health. The present study investigated the effects of partial or complete substitution of CP with sodium bicarbonate (SB) on the physicochemical properties and gel properties of beef-pork-chicken mixed myofibrillar protein (BPC-MP), aiming to evaluate the feasibility of this method in reducing the amount of phosphate in mixed meat products. Under the optimal substitution conditions, the turbidity of BPC-MP was reduced by 37.8%, the net negative potential was increased by 28.9% and the modulus of elasticity (G') was increased. The tertiary structure indexes of protein (including fluorescence intensity, surface hydrophobicity and active thiol content) were significantly changed, whereas the α-helix and β-turn angle contents in the secondary structure of protein were significantly increased. In addition, the water retention ability and strength of gel were also improved, which were increased by 20.7% and 42.6%, respectively. The results of scanning electron microscopy showed that the SB substitution group had a more compact and ordered microstructure. The results showed that partial substitution of CP with SB reduced the amount of phosphate added to BPC-MP and had a positive effect on the physicochemical and gel properties of BPC-MP. © 2024 Society of Chemical Industry.

Green Synthesis and the Evaluation of Osteogenic Potential of Novel Europium-Doped-Monetite Calcium Phosphate by Cissus quadrangularis.

Background The quest for an ideal bone grafting material has been ongoing for decades. Calcium phosphate, alone or in combination with other materials in natural bone, has been shown to aid in bone regeneration effectively. Monetite exhibits superior solubility and resorption rates among calcium phosphates, rendering it an optimal choice for bone regeneration applications. However, the degradation rate of the Monetite is much faster than that of all the other calcium phosphates. Hence, we have added Europium onto the matrix to alter the degradation profile and enhance the osteogenic ability of the prepared matrix. Materials and methods An exclusive Europium-Monetite composite was synthesized employing eco-friendly techniques involving Cissus quadrangularis.The osteogenic potential was gauged using the MG-63 cell line through a calcium mineralization assay employing an Alizarin Red solution, collagen estimation, and an alkaline phosphatase (ALP) assay. The composite's cytocompatibility was evaluated using the MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide)assay across different concentrations ranging from 12.5 µg to 100 µg. Results Scanning electron microscopy (SEM) analysis of the Europium-Monetite composite revealed a sheet-like arrangement in stacks, and the ATR-IR confirmed the presence of elements Ca, P, and Eu. The osteogenic potential, analyzed by ALP activity, calcium mineralization, and collagen staining, was 10% higher than that of the control (Monetite). Conclusion The prepared novel Europium-Monetite calcium phosphate complex can enhance the osteogenic potential and could be a promising material for bone regeneration/tissue engineering. The newly created Europium-Monetite calcium phosphate complex holds promise for various bone grafting applications, including integration into scaffolds and as a coating for implants.

Insight into the interaction between zirconium dibutyl phosphate complex and diluents: An experimental and computational study

In solvent extraction processes, there are challenges caused by the formation of the third phase or interfacial precipitation. The branched alkanes have been used as diluents to disrupt the third-phase formation, while there is little study about the effect of diluents on the appearance of precipitation. Here, we report the inhibiting effect of the novel hyperbranched alkane diluent (HAD) on the formation of zirconium-dibutyl phosphate (Zr-DBP) precipitation and investigate the formation mechanism by the density functional theory (DFT) theory. The extraction experiments show that HAD as the diluent has a remarkable inhibiting ability to form Zr-DBP precipitation, compared with n-dodecane and kerosene. The spectra show no noticeable difference in the composition and structures of the precipitations formed in the three diluents. The energetics from the DFT calculations suggest the P-OH and P=O ligands on one HDBP molecule can bridge two Zr-DBP complexes into a dimer and then aggregate into the precipitation. Besides, the interactions between diluent-diluent molecules play a significant role in precipitation formation. The straight-chain n-dodecanes have a strong intermolecular dispersion force and tend to attract each other but not the Zr-DBP complex. However, the branched alkanes with weak intermolecular interactions have a better dispersive capacity for Zr-DBP complexes, due to the much higher dispersion force of diluent-complex interaction than that of the diluent-diluent interaction. This work provides a new insight into the formation of interfacial crud from the interactions between solutes and diluents of the organic phase in solvent extraction.

Lanthanum-modified tobermorite synthesized from fly ash for efficient phosphate removal.

Phosphate removal from water by lanthanum-modified tobermorite synthesized from fly ash (LTFA) with different lanthanum concentrations was studied. LTFA samples were characterized by X-ray diffraction, Fourier transform infrared spectroscopy, scanning electron microscopy, and Brunauer‒Emmett‒Teller specific surface area analysis. The results showed that the LTFA samples were mainly composed of mesoporous tobermorite-11Å, and LTFA1 with a lanthanum concentration of 0.15M had a high specific surface area (83.82 m2/g) and pore volume (0.6778 cm3/g). The phosphate adsorption capacities of LTFA samples were highest at pH 3 and gradually decreased with increasing pH. The phosphate adsorption kinetics data on LTFA samples were most accurately described by the Elovich model. The adsorption isotherms were in the strongest agreement with the Temkin model, and LTFA1 showed the highest phosphate adsorption capacity (282.51mg P/g), which was higher than that of most other lanthanum-modified adsorbents. LTFA1 presented highly selective adsorption of phosphate with other coexisting ions (HCO3-, Cl-, SO42-, and NO3-). In addition, phosphate was adsorbed onto LTFA samples by forming inner-sphere phosphate complexes and amorphous lanthanum phosphate. This study provides technical support for development of efficient fly ash-based phosphate adsorbents.

Hexavalent chromium removal by green synthesized nano-size iron particles combined with iron sulfides: Effects of dissolved oxygen and phosphate

The removal of hexavalent chromium (Cr(VI)) from wastewater using the green synthesized nano-zero-valent-iron (GnZVI) has attracted great attention. However, the Cr(VI) removal capacity of GnZVI remains limited by dissolved oxygen (DO) or phosphate in wastewater. Therefore, Cr(VI) removal by GnZVI combined with iron sulfides (i.e., FeS or FeS2) impacting by DO and phosphate was investigated at pH 2.0 and 6.0. Experimental results showed that DO inhibited the Cr(VI) removal by GnZVI with FeS at pH 2.0, because high DO saturation was beneficial to Fe(II) oxidization into Fe(III). Nevertheless, DO promoted the corrosion and dissolution of FeS2 but GnZVI for Cr(VI) reduction at pH 2.0. Especially, phosphate inhibited the Cr(VI) reduction by the combination of GnZVI and iron sulfides at pH 2.0, likely because phosphate inhibited Fe(II) release from GnZVI hybrid materials during the reduction process from Cr(VI) to Cr (III). Differently, at pH 6.0, phosphate mainly promoted Cr(VI) removal by FeS compared with GnZVI via the formation of phosphate complexation, while it inhibited Cr(VI) removal using GnZVI combined with FeS2 through the competitive adsorption. This study reveals the potential inherent mechanisms and emphasizes a sustainable strategy for the effective removal of Cr(VI) using a hybrid technique that combines GnZVI and iron sulfides under complex wastewater conditions.

Study the Physical Properties of Fertilizers and Plant Basin Parameters to Design the Tractor Operated Round Basin Maker cum Fertilizer Applicator for Orchard Crop

The physical form of fertilizer production is of extremely importance, both agronomically and in regard to satisfactory handling, transport, storage, and finally application to the field. The improvement of equipment for handling, storage, and application of granular fertilizer require a proper understanding of material properties and flow behavior. The most common problems encountered in fertilizers were caking, poor flow ability, segregation, dustiness and excessive hygroscopicity due to differences of physical properties. The physical properties such as moisture content, angle of repose and bulk density as important in designing the hopper and metering roller of fertilizer plays an important role in the storage, transport and application of fertilizer. The urea, Ammonium phosphate Sulphate, complex fertilizers and fertilizer ratio (10 26 26) per one orchard tree should be applied yearly trice based on crop requirement. The angle of repose value ranges 28° -37° the hopper angle was decided. For that, to flow the fertilizer freely from the hopper, the inclined angle of the hopper should be greater than 40° respectively. The lowest bulk density and tapped density observed 0.648 kg cm-3 and 0.708 kg cm-3 respectively. Coefficient friction for galvanized Iron (GI) material is very high So, based on the obtained results, a fertilizer applicator for orchard crops has been designed. The basin diameter of orchard palm varies from 1500 mm to 1750 mm the mean of 1650 mm. The root zone depth of orchard crop varies from 150 to 180 mm at radius of 1800 mm from the base of palm. The mean 171.66 mm hence depth of operation of machine was selected as 150 mm such that the machine does not interfere with root zone of orchard trees.

Influence of citrate- and phosphate-based calcium sequestering salts on the disruption of casein micelles

The disruption of casein micelles through the addition of calcium sequestering salts (CSS) disodium phosphate (DSP), disodium pyrophosphate (DSPP) and tetrasodium pyrophosphate (TSPP), sodium tripolyphosphate (STPP), sodium hexametaphosphate (SHMP) and trisodium citrate (TSC) at 10, 15, 20 and 30 mEq/L levels was investigated in 5% micellar casein isolate (MCI) solution. All the CSS, except DSPP and TSPP, showed a decrease in particle size and viscosity with increasing concentration. The addition of 10–30 mEq/L of CSS to MCI decreased the protein-bound sedimentable Ca and P at pH 6.5 10 kDa-permeable Ca decreased with increasing concentration of DSP, DSPP, TSPP, STPP and SHMP. These results indicate that orthophosphates, pyrophosphates and polyphosphates combined with Ca to form insoluble Ca phosphate complexes together with casein. Higher amount of 10 kDa permeable Ca for MCI samples with TSC confirms the formation of soluble Ca-citrate complexes.

Effect of Ba(II), Eu(III), and U(VI) on rat NRK-52E and human HEK-293 kidney cells in vitro

Heavy metals pose a potential health risk to humans when they enter the organism. Renal excretion is one of the elimination pathways and, therefore, investigations with kidney cells are of particular interest. In the present study, the effects of Ba(II), Eu(III), and U(VI) on rat and human renal cells were investigated in vitro. A combination of microscopic, biochemical, analytical, and spectroscopic methods was used to assess cell viability, cell death mechanisms, and intracellular metal uptake of exposed cells as well as metal speciation in cell culture medium and inside cells.For Eu(III) and U(VI), cytotoxicity and intracellular uptake are positively correlated and depend on concentration and exposure time. An enhanced apoptosis occurs upon Eu(III) exposure whereas U(VI) exposure leads to enhanced apoptosis and (secondary) necrosis. In contrast to that, Ba(II) exhibits no cytotoxic effect at all and its intracellular uptake is time-independently very low. In general, both cell lines give similar results with rat cells being more sensitive than human cells.The dominant binding motifs of Eu(III) in cell culture medium as well as cell suspensions are (organo-) phosphate groups. Additionally, a protein complex is formed in medium at low Eu(III) concentration. In contrast, U(VI) forms a carbonate complex in cell culture medium as well as each one phosphate and carbonate complex in cell suspensions. Using chemical microscopy, Eu(III) was localized in granular, vesicular compartments near the nucleus and the intracellular Eu(III) species equals the one in cell suspensions.Overall, this study contributes to a better understanding of the interactions of Ba(II), Eu(III), and U(VI) on a cellular and molecular level. Since Ba(II) and Eu(III) serve as inactive analogs of the radioactive Ra(II) and Am(III)/Cm(III), the results of this study are also of importance for the health risk assessment of these radionuclides.