Phosphate Precipitation Research Articles

Guidance on aqueous matrices for evaluating novel precipitants and adsorbents for phosphorus removal and recovery

Phosphorus (P) removal from water and recovery into useable forms is a critical component of creating a sustainable P cycle, although mature technologies for P removal and recovery are still lacking. The goal of this paper was to advance the testing of novel materials for P removal and recovery from water by providing guidance on the development of more realistic aqueous matrices used during materials development. Literature reports of “new” materials to remove P from water are often difficult to compare in terms of performance because authors use a myriad of water chemistries containing P concentrations, pH, and competing ions. Moreover, many tests are conducted in simplified matrices that do not reflect conditions in real systems. To address this critical gap, the research herein developed a systematic approach of identifying aqueous matrices relevant to P recovery, including key components in the aqueous matrices having the greatest influence on the mechanisms of P removal with emphasis on phosphate precipitation and phosphate adsorption, and providing guidelines on relevant “recipes” for aqueous solutions for testing novel materials. Key components in the aqueous matrices included hydrogen ion (i.e., pH), multivalent metal cations, and dissolved organic matter due to their influence on phosphate precipitation and adsorption mechanisms. Recipes for buffer solution and synthetic groundwater, surface water, anaerobic digestate, and stored urine are discussed in the context of P removal and recovery processes. Wherein the adoption of standard matrices in other fields have permitted direct comparison of processes or materials, it is anticipated that adoption of relevant aqueous matrix recipes for P removal and recovery will improve the ability to directly compare novel materials and processes.

Phosphorus removal performance of Sulfide-Based autotrophic denitrification process

Sulfide-based Autotrophic Denitrification (SAD) Process can simultaneous remove sulfurous and nitrogenous pollutants, showing a promising prospect. Beyond our expectation, it also has an efficient phosphorus (P) removal performance. The operation results demonstrated that when the influent concentration of nitrate, sulfide and phosphate was 80.55 ± 2.98 mg N/L, 380.15 ± 20.83 mg S/L and 47.70 ± 4.35 mg P/L respectively, their removal efficiency was 87.63 ± 3.12 %, 99.61 ± 1.02 % and 85.38 ± 4.07 % at the HRT of 8.8 h. However, the phosphorus removal performance disappeared once the effluent pH dropped below 8.0. The random forest regression model revealed that effluent pH had the most significant impact on phosphorus removal performance. This finding was corroborated by a mathematical model that related the phosphate removal load to effluent pHs. The combination of batch test, Standard Measurements and Testing (SMT) and X-Ray Diffraction (XRD) method revealed that the phosphorus removal performance of SAD process came from the synergies of biological phosphorus removal (29.71 ± 3.21 %) and bio-induced phosphate precipitation (70.29 ± 3.21 %). The analysis of key functional genes coding for nitrogen, sulfur and phosphorus metabolism offered an explanation for their metabolic pathways especially the phosphorus removal pathway. The study would provide some new information for the development of SAD process.

Stenotrophomonas pavanii MY01 induces phosphate precipitation of Cu(II) and Zn(II) by degrading glyphosate: performance, pathway and possible genes involved.

Microbial bioremediation is an advanced technique for removing herbicides and heavy metals from agricultural soil. In this study, the strain Stenotrophomonas pavanii MY01 was used for its ability to degrade glyphosate, a phosphorus-containing organic compound, producing PO4 3- as a byproduct. PO4 3- is known to form stable precipitates with heavy metals, indicating that strain MY01 could potentially remove heavy metals by degrading glyphosate. Therefore, the present experiment induced phosphate precipitation from Cu(II) (Hereinafter referred to as Cu2+) and Zn(II) (Hereinafter referred to as Zn2+) by degrading glyphosate with strain MY01. Meanwhile, the whole genome of strain MY01 was mined for its glyphosate degradation mechanism and its heavy metal removal mechanism. The results of the study showed that the strain degraded glyphosate best at 34°C, pH = 7.7, and an inoculum of 0.7%, reaching 72.98% within 3d. The highest removal of Cu2+ and Zn2+ in the test was 75.95 and 68.54%, respectively. A comparison of strain MY01's genome with glyphosate degradation genes showed that protein sequences GE000474 and GE002603 had strong similarity to glyphosate oxidoreductase and C-P lyase. This suggests that these sequences may be key to the strain's ability to degrade glyphosate. The GE001435 sequence appears to be related to the phosphate pathway, which could enable phosphate excretion into the environment, where it forms stable coordination complexes with heavy metals.

Selective Precipitation of REE-Rich Aluminum Phosphate with Low Lithium Losses from Lithium Enriched Slag Leachate.

Currently, recycling of spent lithium-ion batteries is carried out using mechanical, pyrometallurgical and hydrometallurgical methods and their combination. The aim of this article is to study a part of the pyro-hydrometallurgical processing of spent lithium-ion batteries which includes lithium slag hydrometallurgical treatment and refining of the obtained leachate. Leaching was realized via dry digestion, which is an effective method capable of transferring over 99% of the present metals, such as Li, Al, Co, Cu, and others, to the leachate. In this work, the influence of three types of precipitation agents (NaOH, NH4OH, Na3PO4) on the precipitation efficiency of Al and Li losses was investigated. It was found that the precipitation of aluminum with NaOH can result in the co-precipitation of lithium, causing total lithium losses up to 40%. As a suitable precipitating agent for complete Al removal from Li leachate with a minimal loss of lithium (less than 2%), crystalline Na3PO4 was determined under the following conditions: pH = 3, 400 rpm, 10 min, room temperature. Analysis confirmed that, in addition to aluminum, the precipitate also contains the REEs La (3.4%), Ce (2.5%), Y (1.3%), Nd (1%), and Pr (0.3%). The selective recovery of these elements will be the subject of further study.

Experimental evidence that poor soil phosphorus (P) solubility typical of drylands due to calcium co-precipitation favors autonomous plant P acquisition over collaboration with mycorrhizal fungi

Calcareous dryland soils are rich in precipitated phosphate and represent >30% of Earth's land, yet the relative importance of phosphorus-acquisition strategies (PAS) among plant species in these systems is not well known. No experiment has investigated potential interactions between varying amounts of added calcium carbonate (CaCO3) and arbuscular mycorrhizal fungi (AMF) on plant performance and PAS which could test for potential mechanisms without the limitations of in-situ comparisons along natural gradients. To fill this knowledge gap, we conducted an experiment with CaCO3 addition, AMF inoculation, and three invasive and five native grassland plants. We expected an increase in soil [CaCO3] of an alkaline subsoil to 1) reduce soil-available phosphorus (P), 2) reduce plant biomass and P uptake, and 3) shift PAS toward increased root mining as Ca-bound P increases. The largest CaCO3 addition reduced available P by as much as 57%. On average, the largest addition of CaCO3 reduced total biomass of plants by 19% and plant uptake of P by 15%. The PAS seemed to have changed, and CaCO3 additions tended to increase an indicator of root exudation (shoot [Mn]) to mobilize Ca-bound P, suggesting plasticity for some inducible root mining, especially Artemisia frigida and Poa secunda. However, CaCO3 and plant species interacted to affect shoot [Mn]. The invasive grass Bromus tectorum was superior at acquiring P (> P uptake, > shoot [Mn]) and thus tolerating low soluble P conditions. Rarely did AMF and CaCO3 interact to affect plant biomass. When they did, mycorrhizal responsiveness did not increase where P was less available, suggesting AMF become less beneficial upon P and Ca coprecipitation. In dryland soils with less soluble P, plants are thus likely to rely more on root mining PAS than mycorrhizal scavenging, except for the invasive forb Euphorbia esula that always benefitted from AMF inoculation.

The Impact of pH on Fouling and Related Physicochemical Properties of Skim Milk Concentrate during Heat Treatment Using a Laboratory-Scale Fouling Rig.

The objective of this study was to investigate the effect of pH (6.1, 6.3, 6.5, and 6.7) on heat-induced changes in concentrated skim milk as related to fouling in heat exchangers. Skim milk (30%, w/w, total solids) was recirculated in a laboratory-scale fouling rig at an initial target temperature of 85 °C for 90 min to simulate thermal processing and preheating of evaporated liquid concentrate feeds in dairy processing. This study investigated key changes in relevant physicochemical properties, such as viscosity, particle size, and sedimentation, as major contributors to fouling at lower pHs (6.1 and 6.3). Additionally, protein aggregation and calcium phosphate precipitation were identified as significant contributors to fouling deposits. Possible strategies to mitigate fouling were determined, including optimizing pH and adjusting heat treatment parameters to minimize protein denaturation and mineral deposition. The findings indicate that carefully controlling pH and processing parameters can greatly enhance the efficiency of milk concentration by evaporation and tailor finished product quality. Moreover, this study showed that monitoring of CIP solutions for protein content and turbidity provides valuable information on the intensity of fouling and the efficiency of cleaning.

Branched Polymeric Prenucleation Assemblies Initiate Calcium Phosphate Precipitation.

The formation of crystalline calcium phosphate (CaP) has recently gained ample attention as it does not follow the classic nucleation-and-growth mechanism of solid formation. Instead, the precipitation mechanisms can involve numerous intermediates, including soluble prenucleation species. However, structural features, stability, and transformation of such solution-state precursors remain largely undisclosed. Herein, we report a detailed and comprehensive characterization of the sequential events involved in calcium phosphate crystallization starting from the very early prenucleation stage. We integrated an extensive set of time-resolved methods, including NMR, turbidimetry, SAXS, cryo-TEM, and calcium-potentiometry to show that CaP nucleation is initiated by the transformation of "branched" polymeric prenucleation assemblies into amorphous calcium phosphate spheres. Such a mineralization process starts with the spontaneous formation of so-called nanometric prenucleation clusters (PNCs) that later assemble into those branched polymeric assemblies without calcium ion uptake from the solution. Importantly, the branched macromolecular species are invisible to many techniques (NMR, turbidity, calcium-potentiometry) but can readily be evidenced by time-resolved SAXS. We find that these polymeric assemblies constitute the origin of amorphous calcium phosphate (ACP) precipitation through an unexpected process: spontaneous dissolution is followed by local densification of 100-200 nm wide domains leading to ACP spheres of similar size. Finally, we demonstrate that the timing of the successive events involved in the CaP mineralization pathway can be kinetically controlled by the Ca2+/Pi molar ratio, such that the lifetime of the soluble transient species can be increased up to hours when decreasing it.

Design of porous calcium phosphate cement composed of spherical porous granules based on precipitation of octacalcium phosphate

Design of porous calcium phosphate cement composed of spherical porous granules based on precipitation of octacalcium phosphate

Tumour lysis syndrome.

Tumour lysis syndrome (TLS) represents a critical oncological emergency characterized by extensive tumour cell breakdown, leading to the swift release of intracellular contents into the systemic circulation, outpacing homeostatic mechanisms. This process results in hyperuricaemia (a by-product of intracellular DNA release), hyperkalaemia, hyperphosphataemia, hypocalcaemia and the accumulation of xanthine. These electrolyte and metabolic imbalances pose a significant risk of acute kidney injury, cardiac arrhythmias, seizures, multiorgan failure and, rarely, death. While TLS can occur spontaneously, it usually arises shortly after the initiation of effective treatment, particularly in patients with a large cancer cell mass (defined as ≥500 g or ≥300 g/m2 of body surface area in children). To prevent TLS, close monitoring and hydration to improve renal perfusion and urine output and to minimize uric acid or calcium phosphate precipitation in renal tubules are essential. Intervention is based on the risk of a patient of having TLS and can include rasburicase and allopurinol. Xanthine, typically enzymatically converted to uric acid, can accumulate when xanthine oxidases, such as allopurinol, are administered during TLS management. Whether measurement of xanthine is clinically useful to optimize the use of allopurinol or rasburicase remains to be determined.

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.

Impact of additives on syntrophic propionate and acetate enrichments under high-ammonia conditions

High ammonia concentrations in anaerobic degradation systems cause volatile fatty acid accumulation and reduced methane yield, which often derive from restricted activity of syntrophic acid-oxidising bacteria and hydrogenotrophic methanogens. Inclusion of additives that facilitate the electron transfer or increase cell proximity of syntrophic species by flocculation can be a suitable strategy to counteract these problems, but its actual impact on syntrophic interactions has yet to be determined. In this study, microbial cultivation and molecular and microscopic analysis were performed to evaluate the impact of conductive (graphene, iron oxide) and non-conductive (zeolite) additives on the degradation rate of acetate and propionate to methane by highly enriched ammonia-tolerant syntrophic cultures derived from a biogas process. All additives had a low impact on the lag phase but resulted in a higher rate of acetate (except graphene) and propionate degradation. The syntrophic bacteria ‘Candidatus Syntrophopropionicum ammoniitolerans’, Syntrophaceticus schinkii and a novel hydrogenotrophic methanogen were found in higher relative abundance and higher gene copy numbers in flocculating communities than in planktonic communities in the cultures, indicating benefits to syntrophs of living in close proximity to their cooperating partner. Microscopy and element analysis showed precipitation of phosphates and biofilm formation in all batches except on the graphene batches, possibly enhancing the rate of acetate and propionate degradation. Overall, the concordance of responses observed in both acetate- and propionate-fed cultures highlight the suitability of the addition of iron oxide or zeolites to enhance acid conversion to methane in high-ammonia biogas processes.Key points• All additives promoted acetate (except graphene) and propionate degradation.• A preference for floc formation by ammonia-tolerant syntrophs was revealed.• Microbes colonised the surfaces of iron oxide and zeolite, but not graphene.Graphical

Iron cycling and isotopic fractionation in a ferruginous, seasonally ice-covered lake

Ferruginous conditions, defined by anoxia and abundant dissolved ferrous iron (Fe2+aq), dominated the Precambrian oceans but are essentially non-existent in a modern, oxygenated world. Ferruginous meromictic lakes represent natural laboratories to ground truth our understanding of the stable Fe isotope proxy, which has been used extensively in interpreting the origins of Fe-rich sedimentary rocks like iron formations (IFs) and the interactions of early life with high-Fe2+aq conditions. Here we report comprehensive geochemical and Fe isotopic analyses of samples collected in May and August 2022, and March 2023, from Deming Lake, Minnesota, a ferruginous meromictic lake that undergoes surface freezing in winter and never becomes euxinic. Through chemical and Fe isotopic analyses of different putative Fe sources to Deming Lake; including eolian input trapped in winter ice cover, nearby bogs, and regional groundwaters sampled at surface springs; we find that a groundwater source provides the best chemical and Fe isotopic match for Deming Lake and can support Fe2+aq-rich waters at depth that maintain a permanent chemocline at ∼12 m. The ice-free Deming Lake water column can be split into three layers dominated by distinct Fe cycling regimes. Layer (I) extends from the lake surface to the base of the oxycline at ∼6 m, and its Fe cycling is dominated by isotopically light Fe uptake into biomass, likely from stabilized dissolved Fe3+, with variable eolian lithogenic influences. Layer (II) extends between the oxycline and the chemocline at ∼12 m and is dominated by partial Fe2+aq oxidation on approach to the oxycline, with the formation of variably isotopically heavy Fe3+-bearing particles. Layer (III) underlies the chemocline and is defined by Fe2+ phosphate (vivianite) and carbonate saturation and precipitation under anoxic, Fe2+aq-rich conditions with little Fe isotopic fractionation. The ice-covered winter water column features more homogenous Fe chemistry above the chemocline, which we attribute to seasonal homogenization of Layers (I) and (II), with suppressed ferric particle formation. Authigenic Fe minerals with non-crustal (light) Fe isotopic compositions only appreciably accumulate in sediments in Deming Lake underlying the chemocline. All sediments deposited above 12 m appear crustal in their Fe isotopic, Mn/Fe, and Fe/Al ratios, likely revealing efficient reductive dissolution of Fe3+-bearing lake precipitates and remineralization of Fe-bearing biomass. We find limited fractionation of Fe isotopes in the ice-covered water column and suggest this provides evidence that substantial delivery of oxidants is required to generate highly fractionated Fe isotopic compositions in Sturtian Snowball era IFs. By comparing Fe isotopic and Mn/Fe fractionation trends in the different Deming Lake layers, we also suggest that correlations between these two parameters in giant early Paleoproterozoic IFs requires the simultaneous deposition of multiple authigenic phases on the ancient seafloor. Finally, high-precision triple Fe isotopic analyses of dissolved Fe impacted by extensive oxidation near the Deming Lake oxycline reveal that the slope of the mass fractionation law for natural, O2-mediated Fe2+aq oxidation is identical to those previously defined for both UV photo-oxidation, and for an array of highly fractionated Paleoproterozoic IFs.

Immobilization of Heavy Metals by Phosphorus-solubilizing Bacteria and Inhibition of Cd and Pb Uptake by Wheat

Phosphorus-solubilizing microorganisms convert insoluble phosphorus in the soil into phosphorus that can be absorbed by plants. Soluble phosphate combines with heavy metals to form precipitation, reducing the content of available heavy metals, thereby reducing the absorption of heavy metals by crops, which plays an important role in the remediation of heavy metal-contaminated soil. The effects of the immobilization of Cd and Pb and the release of PO43- by the phosphorus-solubilizing bacterium Klebsiella sp. M2 were studied through solution culture experiments. In addition, the effects of strain M2 on wheat uptake of Cd and Pb and its microbiological mechanism were also explored through pot experiments. The results showed that strain M2 reduced the concentrations of Cd and Pb and increased the concentration of PO43- in the solution through cell wall adsorption and induced phosphate precipitation. Pot experiments showed that compared to those in the CK group and inactivated strain M2 group, inoculation with live strain M2 significantly increased （123%-293%） the contents of Ca2-P and Ca8-P in rhizosphere soil, decreased the content of DTPA-Cd （34.48%） and DTPA-Pb （36.72%） in wheat rhizosphere soil, and thus hindered the accumulation of Cd and Pb in wheat grains. Moreover, high-throughput sequencing results showed that strain M2 significantly increased the diversity of wheat rhizosphere bacterial communities； increased the relative abundance of Proteobacteria, Gemmatimonadetes, and Bacteroidota in wheat rhizosphere soil； and increased the proportion of heavy metal-immobilizing and phosphorus-promoting bacteria in wheat rhizosphere soil （mainly Sphingomonas, Nocardioides, Bacillus, Gemmatimonas, and Enterobacter）. These bacterial genera played an important role in immobilizing heavy metals and preventing wheat from absorbing heavy metals. These results provide bacterial resources and theoretical basis for the bioremediation of heavy metal-contaminated farmland.

The effect of bacteria on uranium sequestration stability by different forms of phosphorus

ABSTRACT Immobilisation of uranium (U (VI)) by direct precipitation of uranyl phosphate (U-P) exhibits a great potential application in the remediation of U (VI)-contaminated environments. However, phosphorus, vital element of bacteria’s decomposition, absorption and transformationmay affect the stability of U (VI) with ageing time. The main purpose of this work is to study the effect of bacteria on uranium sequestration mechanism and stability by different forms of phosphorus in a water sedimentary system. The results showed that phosphate effectively enhanced the removal of U (VI), with 99.84%. X-Ray Diffraction (XRD), Scanning Electron Microscopy and Energy Dispersive Spectrometer (SEM-EDS), and X-ray Photoelectron Spectroscopy (XPS) analyses imply that U (VI) and U (IV) co-exist on the surface of the samples. Combined with BCR results, it demonstrated that bacteria and phosphorus have a synergistic effect on the removal of U (VI), realising the immobilisation of U (VI) from a transferable phase to a stable phase. However, from a long-term perspective, the redissolution and release of uranium immobilisation of U (VI) by pure bacteria with ageing time are worthy of attention, especially in uranium mining environments rich in sensitive substances. This observation implies that the stability of the uranium may be impacted by the prevailing environmental conditions. The novel findings could provide theoretical evidence for U (VI) bio-immobilisation in U (VI)-contaminated environments.

Branched polymer grafted graphene oxide (GO) as a 2D template for calcium phosphate growth

HypothesisGraphene Oxide (GO)-templated deposition of inorganic materials through synthesis on dispersed single sheets of GO is often complicated by the loss of the desired 2D morphology owing to the coagulation of GO sheets at high salt concentrations and non-templated homogenous nucleation. Modifying GO with anionic polymer is expected to solve both problems by i) enhancing electrostatic(steric) stabilization upon exposure to high concentrations of the ionic precursors, and ii) offering additional nucleation sites at the grafted anionic moieties to avoid homogeneous secondary nucleation. ExperimentsGO was grafted with branched copolymers of poly(ethylene glycol) methacrylate (PEGMA 500) and diethylene glycol dimethacrylate (DEGDMA) and ω-vinyl terminated methacrylic acid macromonomer (P(MAA)), the latter serving as an addition-fragmentation chain transfer agent. The colloidal stability of GO dispersions in water toward salt was evaluated before and after modification. Precipitation of calcium phosphate (CaP) was performed by incubating modified GO in the precursor solutions. The conditions were optimized to maximize the nucleation selectively onto GO without homogeneous CaP nucleation and coagulation of the GO-sheets. FindingsThe copolymer grafted GO-sheets shows superior colloidal stability when dispersed in water. No aggregation occurs in the incubating ionic CaP precursor solutions. The optimum templated deposition of CaP onto the GO sheets by precipitation is to add a second shot of precursors after the nucleation stage to obtain GO sheets fully decorated with calcium phosphate nanorods without self-nucleation. Via the careful design on the GO modification and incubation process, the growth of calcium phosphate nanorods were confined in the desired 2D order exclusively, hereby achieving the goal of an efficient GO-templated synthesis.

Non-industrial production of therapeutic lentiviral vectors: How to provide vectors to academic CAR-T.

Bringing effective cancer therapy in the form of chimeric antigen receptor technology to untapped markets faces numerous challenges, including a global shortage of therapeutic lentiviral or retroviral vectors on which all current clinical therapies using genetically modified T cells are based. Production of these lentiviral vectors in academic settings in principle opens the way to local production of therapeutic cells, which is the only economically viable approach to make this therapy available to patients in developing countries. The conditions for obtaining and concentrating lentiviral vectors have been optimized and described. The calcium phosphate precipitation method was found to be suitable for transfecting high cell-density cultures, a prerequisite for high titers. We describe protocols for gradually increasing production from 6-well plates to P100 plates, T-175 flasks, and 5-layer stacks while maintaining high titers, >108 transducing units. Concentration experiments using ultracentrifugation revealed the advantage of lower centrifugation speeds compared to competing protocols. The resulting batches of lentiviral vectors had a titer of 1010 infectious particles and were used to transduce primary human T lymphocytes generating chimeric antigen receptor T cells, the quality of which was checked and found potential applicability for treatment.

Development of Rapid Bioactivity-Expressed Zr-50Ti Alloys by Surface Treatment with Modified Simulated Body Fluid.

Zr-50Ti alloys are promising biomaterials due to their excellent mechanical properties and low magnetic susceptibility. However, Zr-50Ti alloys do not inherently bond well with bone. This study aims to enhance the bioactivity and bonding strength of Zr-50Ti alloys for orthopedic implant materials. Initially, the surface of Zr-50Ti alloys was treated with a sulfuric acid solution to create a microporous structure, increasing surface roughness and area. Subsequently, low crystalline calcium phosphate (L-CaP) precipitation was controlled by adding Mg2+ and/or CO32- ions in modified simulated body fluid (m-SBF). The treated Zr-50Ti alloys were then subjected to cold isostatic pressing to force m-SBF into the micropores, followed by incubation to allow L-CaP formation. The apatite-forming process was tested in simulated body fluid (SBF). The results demonstrated that the incorporation of Mg2+ and/or CO32- ions enabled the L-CaP to cover the entire surface of Zr-50Ti alloys within only one day. After short-term soaking in SBF, the L-CaP layer, modulated by Mg2+ and/or CO32- ions, formed a uniform hydroxyapatite (HA) coating on the surface of the Zr-50Ti alloys, showing potential for optimized bone integration. After soaking in SBF for 14 days, the bonding strength between the apatite layer and alloy has the potential to meet the orthopedic application requirement of 22 MPa. This study demonstrates an effective method to enhance the bioactivity and bonding strength of Zr-50Ti alloys for orthopedic applications.

Phosphorus recovery from hydroponics waste nutrient solution and its economic potential

Nutrient management, particularly phosphorus, is crucial for global food security due to its limited availability. This study investigates the extraction of phosphorus from hydroponic waste nutrient solutions (HWNS) using samples from various hydroponic farms. The results display elevated phosphorus levels, peaking at 70 mg/L and a median of 20 mg/L, in conjunction with a high median calcium concentration of 220 mg/L. This combination enhances the potential for efficient calcium phosphate precipitation. At a pH of 9.5, phosphorus removal reached consistently high levels, exceeding 94 % and achieving a median value of 97.6 %. The economic value of the recovered phosphorus was then compared to rock phosphates. Through chemical precipitation with micro-calcium phosphate, economic evaluations determined that to achieve production costs comparable to or below the market value of calcium phosphate, HWNS should contain a phosphorus concentration of at least 16 mg P/L and 12.4 mg P/L in the context of Australian and international markets, respectively.

Phosphate as an adjunct to calcium in promoting coronary vascular calcification in chronic inflammatory states.

Bone releases calcium and phosphate in response to pro-inflammatory cytokine-mediated inflammation. The body develops impaired urinary excretion of phosphate with age and chronic inflammation given the reduction of the kidney protein Klotho, which is essential to phosphate excretion. Phosphate may also play a role in the development of the resistance of the parathyroid calcium-sensing receptor (CaSR) to circulating calcium thus contributing to calcium retention in the circulation. Phosphate can contribute to vascular smooth muscle dedifferentiation with manifestation of osteoblastogenesis and ultimately endovascular calcium phosphate precipitation. Thus phosphate, along with calcium, contributes to the calcification and inflammation of atherosclerotic plaques and the origin of these elements is likely the bone, which serves as storage for the majority of the body's supply of extracellular calcium and phosphate. Early cardiac evaluation of patients with chronic inflammation and attempts at up-regulating the parathyroid CaSR with calcimimetics or introducing earlier anti-resorptive treatment with bone active pharmacologic agents may serve to delay onset or reduce the quantity of atherosclerotic plaque calcification in these patients.

Recovery of iron phosphate and lithium carbonate from sulfuric acid leaching solutions of spent LiFePO4 batteries by chemical precipitation

The recycling of lithium and iron from spent lithium iron phosphate (LiFePO<sub>4</sub>) batteries has gained attention due to the explosive growth of the electric vehicle market. To recover both of these metal ions from the sulfuric acid leaching solution of spent LiFePO<sub>4</sub> batteries, a process based on precipitation was proposed in this study. Since ferric and ferrous ions coexisted in the leaching solution, all the ferrous ions were first oxidized to ferric ions by adding H<sub>2</sub>O<sub>2</sub> to the leaching solution. About 99% iron(III) was recovered as iron phosphate by adjusting the solution pH to 2 at 25 <sup>o</sup>C for 30 mins. After the precipitation of iron phosphate, the remaining Li(I) in the filtrate was recovered as lithium carbonate by precipitation with Na<sub>2</sub>CO<sub>3</sub> as a precipitant. Addition of acetone to the filtrate at room temperature greatly enhanced the precipitation percentage of Li(I). Moreover, solid Na<sub>2</sub>CO<sub>3</sub> was better than Na<sub>2</sub>CO<sub>3</sub> solution in precipitating Li(I). About 95% of lithium ions was recovered as carbonate precipitates under the optimum conditions: solution pH = 11, 3.0 molar ratio of solid Na<sub>2</sub>CO<sub>3</sub> to Li(I), 7/5(v/v) volume ratio of acetone to the filtrate, 25 <sup>o</sup>C, 300 rpm for 2 hrs.