Phosphate Solution Research Articles

An Experimental study on steam explosion of multiple droplets in different chemical solutions

Motivated by the interest in steam explosion in chemical solutions and seawater, a series of tests were carried out in the MISTEE facility at KTH to investigate steam explosion characteristics as multiple molten droplets of tin were falling through a coolant pool containing deionized water, boric acid solution, neutral solution of boric acid and sodium phosphate, and seawater, separately. The experimental results revealed distinct and complex characteristics of steam explosion of multiple droplets, which were not observed in previous single-droplet steam explosion experiments. The tin melt samples of 5 g and 20 g were employed to formulate different numbers of multiple droplets. In the test with 5 g melt, steam explosion was more energetic at a deeper explosion location − a similar trend found in the single-droplet steam explosion test with 1 g melt. However, the test of 20 g melt did not show a clear trend in a wide range of explosion depth. The peak pressure and impulse increased with increasing mass of melt sample. The steam explosion occurred more closely to the coolant pool surfaces in the seawater and chemical solutions than in deionized water. Steam explosion intensity was significantly reduced in a neutral solution containing 1.2 wt.% boric acid and sodium phosphate. The influence of the chemical solutions on steam explosion was diminishing in the tests with multiple droplets.

Temperature, pressure, and duration impacts on the optimal stiffening of carbonates aged in diammonium phosphate solution

Diammonium phosphate (DAP) has been proven effective in improving the stiffness of weak or acid-damaged carbonates, thereby preserving hydraulic fracture conductivity. The reaction between DAP and calcite in chalk formations primarily produces hydroxyapatite (HAP), which is stiffer than calcite. However, the optimal reaction outcomes vary greatly with factors such as DAP concentration and reaction conditions. This study investigated the DAP-calcite reaction duration, pressure, and temperature effects on the stiffness magnitude of soft Austin chalk. Also, the catalyst effect and depth of HAP formation were examined. The study involved the assessment of stiffness non-destructively (impulse hammering), mineralogy (XRD, SEM), and elemental composition (XRF). The study tested 15 different DAP-chalk reaction variations, where the pressure, temperature, aging time and catalyst addition were modified in each case. The samples' elastic stiffness distributions were then collected and compared to the pre-reaction ones. The results showed that the elastic stiffness increased in all treated samples, with an 181% maximum increase achieved after 72 h at 6.9 MPa and 75 °C. However, the pressure effect was minor compared to the temperature. The SEM images revealed different HAP morphology corresponding to different treatment conditions. Although the treated samples showed an increased intensity of phosphorus throughout the entire sample, the near-surface zone (4–6 mm) was the most affected, as inferred from the XRF elemental analysis. The study's findings can help optimize hydraulic fracturing operations in weak carbonate reservoirs, improving production rates and overall well performance.

Mechanical stretch leads to increased caveolin-1 content and mineralization potential in extracellular vesicles from vascular smooth muscle cells

BackgroundHypertension-induced mechanical stress on vascular smooth muscle cells (VSMCs) is a known risk factor for vascular remodeling, including vascular calcification. Caveolin-1 (Cav-1), an integral structural component of plasma membrane invaginations, is a mechanosensitive protein that is required for the formation of calcifying extracellular vesicles (EVs). However, the role of mechanics in Cav-1-induced EV formation from VSMCs has not been reported.ResultsExposure of VSMCs to 10% mechanical stretch (0.5 Hz) for 72 h resulted in Cav-1 translocation into non-caveolar regions of the plasma membrane and subsequent redistribution of Cav-1 from the VSMCs into EVs. Inhibition of Rho-A kinase (ROCK) in mechanically-stimulated VSMCs exacerbated the liberation of Cav-1 positive EVs from the cells, suggesting a potential involvement of actin stress fibers in this process. The mineralization potential of EVs was measured by incubating the EVs in a high phosphate solution and measuring light scattered by the minerals at 340 nm. EVs released from stretched VSMCs showed higher mineralization potential than the EVs released from non-stretched VSMCs. Culturing VSMCs in pro-calcific media and exposure to mechanical stretch increased tissue non-specific alkaline phosphatase (ALP), an important enzyme in vascular calcification, activity in EVs released from the cells, with cyclic stretch further elevating EV ALP activity compared to non-stretched cells.ConclusionOur data demonstrate that mechanical stretch alters Cav-1 trafficking and EV release, and the released EVs have elevated mineralization potential.

Citrate Improves Biomimetic Mineralization Induced by Polyelectrolyte-Cation Complexes Using PAsp-Ca&Mg Complexes.

Magnesium ions are highly enriched in early stage of biological mineralization of hard tissues. Paradoxically, hydroxyapatite (HAp) crystallization is inhibited significantly by high concentration of magnesium ions. The mechanism to regulate magnesium-doped biomimetic mineralization of collagen fibrils has never been fully elucidated. Herein, it is revealed that citrate can bioinspire the magnesium-stabilized mineral precursors to generate magnesium-doped biomimetic mineralization as follows: Citrate can enhance the electronegativity of collagen fibrils by its absorption to fibrils via hydrogen bonds. Afterward, electronegative collagen fibrils can attract highly concentrated electropositive polyaspartic acid-Ca&Mg (PAsp-Ca&Mg) complexes followed by phosphate solution via strong electrostatic attraction. Meanwhile, citrate adsorbed in/on fibrils can eliminate mineralization inhibitory effects of magnesium ions by breaking hydration layer surrounding magnesium ions and thus reduce dehydration energy barrier for rapid fulfillment of biomimetic mineralization. The remineralized demineralized dentin with magnesium-doped HAp possesses antibacterial ability, and the mineralization mediums possess excellent biocompatibility via cytotoxicity and oral mucosa irritation tests. This strategy shall shed light on cationic ions-doped biomimetic mineralization with antibacterial ability via modifying collagen fibrils and eliminating mineralization inhibitory effects of some cationic ions, as well as can excite attention to the neglected multiple regulations of small biomolecules, such as citrate, during biomineralization process.

Oxygen Isotope Analysis of Nanomole Phosphate Using PO3- Fragment in ESI-Orbitrap-MS.

The oxygen isotope composition of phosphate is a useful tool for studying biogeochemical phosphorus cycling. However, the current Ag3PO4 method is not only tedious in PO43- extraction and purification but also requires a large-sized sample at the micromole level, thereby limiting its application. Here, we present an approach to measuring the oxygen isotope composition, δ18O, of dissolved phosphate at the nanomole level using electrospray ionization Orbitrap mass spectrometry (ESI-Orbitrap-MS). We compared the reproducibility of δ18O measurements using the H2PO4- ions (m/z = 97 and 99 for H2P16O4- and H2P18O16O3-, respectively) and using the PO3- fragment ions (m/z = 79 and 81 for P16O3- and P18O16O2-, respectively) generated by source fragmentation and by higher-energy collisional dissociation, respectively. The results demonstrate that phosphate δ18O can be more reliably measured by the PO3- ions than by the H2PO4- ions. PO3- generated by source fragmentation at 40 V achieved the highest reproducibility for δ18O based on precision tests. Furthermore, the mass spectrum for a 50:50 μM mixed solution of phosphate and sulfate revealed that PO3- ions resulting from source fragmentation at 40 V are the predominant species in the Orbitrap analyzer. Notably, P16O3- ions (m/z: 79) are not interfered with by 32S16O3- (m/z: 80) ions. This is in contrast to the case for 1H2P16O4- ions, which share the same m/z value with 1H32S16O4- ions and exhibit much lower signal intensity than HSO4- ions. Using the PO3- fragment method and six phosphate standards with a wide range of δ18O values, we obtained a calibration line with a slope of 0.94 (R2 = 0.98). The overall uncertainty for ESI-Orbitrap-MS phosphate δ18O measurement was 0.8‰ (n = 30; 1 SD). With much room for improvement, the PO3- fragment method presents a better approach to measuring the phosphate oxygen isotope composition, applicable to nanomole sample sizes in a liquid phase.

Amelogenin-inspired peptide, calcium phosphate solution, fluoride and their synergistic effect on enamel biomimetic remineralization: an in vitro pH-cycling model

BackgroundSeveral methods were introduced for enamel biomimetic remineralization that utilize a biomimetic analogue to interact and absorb bioavailable calcium and phosphate ions and induce crystal nucleation on demineralized enamel. Amelogenin is the most predominant enamel matrix protein that is involved in enamel biomineralization. It plays a major role in developing the enamel’s hierarchical microstructure. Therefore, this study was conducted to evaluate the ability of an amelogenin-inspired peptide to promote the remineralization potential of fluoride and a supersaturated calcium phosphate solution in treating artificially induced enamel carious lesions under pH-cycling regimen.MethodsFifty enamel slices were prepared with a window (4*4 mm2 ) on the surface. Five samples were set as control healthy enamel and 45 samples were subjected to demineralization for 3 days. Another 5 samples were set as control demineralized enamel and 40 enamel samples were assigned into 8 experimental groups (n=5) (P/I, P/II, P/III, P/AS, NP/I, NP/II, NP/III and NP/AS) according to peptide treatment (peptide P or non-peptide NP) and remineralizing solution used (I; calcium phosphate solution, II; calcium phosphate fluoride solution, III; fluoride solution and AS; artificial saliva). Samples were then subjected to demineralization/remineralization cycles for 9 days. Samples in all experimental groups were evaluated using Raman spectroscopy for mineral content recovery percentage, microhardness and nanoindentation as healthy, demineralized enamel and after pH-cycling. Data were statistically analysed using two-way repeated measures Anova followed by Bonferroni-corrected post hoc test for pairwise multiple comparisons between groups. Statistical significance was set at p= 0.05. Additionally, XRD, FESEM and EDXS were used for crystal orientation, surface morphology and elemental analysis after pH-cycling.ResultsNanocrystals clumped in a directional manner were detected in peptide-treated groups. P/II showed the highest significant mean values in mineral content recovery (63.31%), microhardness (268.81±6.52 VHN), elastic modulus (88.74±2.71 GPa), nanohardness (3.08±0.59 GPa) and the best crystal orientation with I002/I300 (1.87±0.08).ConclusionDespite pH changes, the tested peptide was capable of remineralizing enamel with ordered crystals. Moreover, the supplementary use of calcium phosphate fluoride solution with peptide granted an enhancement in enamel mechanical properties after remineralization.

Effect of Various Sizes of Calcined Marsh Clam Shell on Phosphate Removal from Aqueous Solution

Phosphorus is one of essential elements for sustaining life largely through phosphate, a compound containing the phosphate ion, PO43−. However, excessive phosphorus concentrations will cause eutrophication and this condition is considered as an environmental issue. The phosphorus sources are commonly from human activities; for instance, detergents, fertilisers, and industries. Although various adsorption techniques have been applied to remove phosphorus in water, the effect of different particle sizes of calcined marsh clam shells on phosphate removal has not been fully investigated, along with its adsorption kinetics and isotherms. This study investigates phosphate removal from synthetic solution onto calcined marsh clam shells (CMCs) with 5 different particle sizes: 0.075–0.15, 0.15–0.30, 0.30–0.60, 0.60–1.18, and 1.18–2.36 mm. The batch experiment used 2 g of adsorbent and synthetic potassium dihydrogen phosphate (KH2PO4) solution. The adsorbent size of 0.075 to 0.15 mm showed the highest removal (100%) efficiency due to high adsorption rate. The experimental data were further analysed using kinetics and isotherm models; the data fitted well with pseudo-second-order kinetic model (R2 = 0.9986) and Freundlich isotherm model (R2 = 0.8404). The potential of marsh clam shells as an adsorbent for phosphate removal in water is significant for future applications in wastewater treatment technology.

Reverse‐phase high‐performance liquid chromatography methodology for film‐forming mafenide spray: Compatibility, assay, and in‐vitro release evaluation using Franz vertical diffusion cell apparatus

AbstractThis paper described a short and precise reverse‐phase high‐performance liquid chromatography (HPLC) method for quantifying mafenide in a film‐forming spray and preliminary in‐vitro release study. Following the International Council for Harmonization guidelines Q2 (R1), the method was validated. The chromatographic separation was achieved using a 10 mM potassium dihydrogen phosphate solution (mobile phase A) mixed with HPLC‐grade methanol (mobile phase B) in an 85:15 v/v ratio. Inert Sustain C8 (4.6 × 250 mm), 5 μm column was selected as the stationary phase. The flow rate was set as 0.8 mL/min, and detection was carried out at a wavelength of 222 nm. The developed HPLC method showed an accuracy between 98% and 102%. The primary diffusion study of film‐forming spray was performed using the Franz vertical diffusion cell apparatus. It was observed that an average of 26.94% of drug releases at 24 h. This indicates the drug has a slower release rate and shows local pharmacological action. The Weibull dissolution model was more fitting with regression square 0.9953. Furthermore, the drug excipient compatibility study revealed no interactions as the only drug peak was found in the chromatographic method, indicating that the chosen excipients were appropriate for a stable formulation.

Novel high-voltage cathode for aqueous zinc ion batteries: Porous K0.5VOPO4·1.5H2O with reversible solid-solution intercalation and conversion storage mechanism

Cathode materials that possess high output voltage, as well as those that can be mass-produced using facile techniques, are crucial for the advancement of aqueous zinc-ion battery (ZIBs) applications. Herein, we present for the first time a new porous K0.5VOPO4·1.5H2O polyanionic cathode (P-KVP) with high output voltage (above 1.2 V) that can be manufactured at room temperature using straightforward coprecipitation and etching techniques. The P-KVP cathode experiences anisotropic crystal plane expansion via a sequential solid-solution intercalation and phase conversion pathway throughout the Zn2+ storage process, as confirmed by in-situ synchrotron X-ray diffraction and ex-situ X-ray photoelectron spectroscopy. Similar to other layered vanadium-based polyanionic materials, the P-KVP cathode experiences a progressive decline in voltage during the cycle, which is demonstrated to be caused by the irreversible conversion into amorphous VOx. By introducing a new electrolyte containing Zn(OTF)2 to a mixed triethyl phosphate and water solution, it is possible to impede this irreversible conversion and obtain a high output voltage and longer cycle life by forming a P-rich cathode electrolyte interface layer. As a proof-of-concept, the flexible fiber-shaped ZIBs based on modified electrolyte woven into a fabric watch band can power an electronic watch, highlighting the application potential of P-KVP cathode.

Novel in vitro evidence on the beneficial effect of quercetin treatment in vascular calcification.

Vascular calcification is a pathological chronic condition characterized by calcium crystal deposition in the vessel wall and is a recurring event in atherosclerosis, chronic kidney disease, and diabetes. The lack of effective therapeutic treatments opened the research to natural products, which have shown promising potential in inhibiting the pathological process in different experimental models. This study investigated the anti-calcifying effects of Quercetin and Berberine extracts on vascular smooth muscle cells (VSMCs) treated with an inorganic phosphate solution for 7days. Quercetin has shown the highest anti-calcifying activity, as revealed by the intracellular quantitative assay and morphological analysis. Confocal microscopy revealed downregulation of RUNX2, a key marker for calcified phenotype, which was otherwise upregulated in calcified VSMCs. To investigate the anti-inflammatory activity of Quercetin, culture media were subjected to immunometric assays to quantify the levels of IL-6 and TNF-α, and the caspase-1 activity. As expected, calcified VSMCs released a large quantity of inflammatory mediators, significantly decreasing in the presence of Quercetin. In summary, our findings suggest that Quercetin counteracted calcification by attenuating the VSMC pathological phenotypic switch and reducing the inflammatory response. In our opinion, these preliminary in vitro findings could be the starting point for further investigations into the beneficial effects of Quercetin dietary supplementation against vascular calcification.

Fluoride-Incorporated Apatite Coating on Collagen Sponge as a Carrier for Basic Fibroblast Growth Factor.

Coating layers consisting of a crystalline apatite matrix with immobilized basic fibroblast growth factor (bFGF) can release bFGF, thereby enhancing bone regeneration depending on their bFGF content. We hypothesized that the incorporation of fluoride ions into apatite crystals would enable the tailored release of bFGF from the coating layer depending on the layer's fluoride content. In the present study, coating layers consisting of fluoride-incorporated apatite (FAp) crystals with immobilized bFGF were coated on a porous collagen sponge by a precursor-assisted biomimetic process using supersaturated calcium phosphate solutions with various fluoride concentrations. The fluoride content in the coating layer increased with the increasing fluoride concentration of the supersaturated solution. The increased fluoride content in the coating layer reduced its solubility and suppressed the burst release of bFGF from the coated sponge into a physiological salt solution. The bFGF release was caused by the partial dissolution of the coating layer and, thus, accompanied by the fluoride release. The concentrations of released bFGF and fluoride were controlled within the estimated effective ranges in enhancing bone regeneration. These findings provide useful design guidelines for the construction of a mineralized, bFGF-releasing collagen scaffold that would be beneficial for bone tissue engineering, although further in vitro and in vivo studies are warranted.

Preparation and Morphology Control of Hydroxyapatite by Aqueous Precipitation

Hydroxyapatite, with excellent biocompatibility, biological activity, and biological affinity, is the main inorganic component of human bones and teeth. It can promote bone tissue regeneration and has important applications in bone tissue engineering fields such as bone defect repair and bone replacement. In this study, calcium acetate solution and diammonium dihydrogen phosphate solution had been mixed to prepare calcium phosphate through aqueous precipitation reaction. The testing results of scanning electron microscopy and X-ray diffraction show that the morphology of the product can be controlled by changing the pH, the temperature, and the method of adding reactant solution dropwise. When the temperature of the reaction system is 20℃, plate-like calcium hydrogen phosphate is mainly obtained; block-like hydroxyapatite is obtained when the temperature rised to 40℃; and needle shaped hydroxyapatite is obtained at 60℃. The length and diameter of two-dimensional hydroxyapatite crystals become smaller when the temperature and the pH value of the reaction system increase.

A Visible Light Cross-Linked Underwater Hydrogel Adhesive with Biodegradation and Hemostatic Ability.

Hydrogel adhesives with integrated functionalities are still required to match their ever-expanding practical applications in the field of tissue repair and regeneration. A simple and effective safety strategy is reported, involving an in situ injectable polymer precursor and visible light-induced cross-linking. This strategy enables the preparation of a hydrogel adhesive in a physiological environment, offering wet adhesion to tissue surfaces, molecular flexibility, biodegradability, biocompatibility, efficient hemostatic performance, and the ability to facilitate liver injury repair. The proposed one-step preparation process of this polymer precursor involves the mixing of gelatin methacryloyl (GelMA), poly(thioctic acid) [P(TA)], poly(acrylic acid)/amorphous calcium phosphate (PAAc/ACP, PA) and FDA-approved photoinitiator solution, and a subsequent visible light irradiation after in situ injection into target tissues that resulted in a chemically-physically cross-linked hybrid hydrogel adhesive. Such a combined strategy shows promise for medical scenarios, such as uncontrollable post-traumatic bleeding.

Synthesis and characterization of strontium substituted monetite coatings via mild phosphate chemical conversion

Strontium (Sr) substitution into calcium phosphate (CaP) materials has gained acceptance in research into the enhancement of physiochemical and osteogenic potential. Conventional synthesis of metal cationic substitution into CaP coatings on metal substrate usually takes relatively high temperature (﹥100 °C) and hours of processing time. Herein, a mild phosphate chemical conversion method was developed for preparing Sr-substituted CaP coatings on surface of titanium (Ti) in the presence of increasing amount of Sr (40–60 mol%). The results indicated that the complete and even coatings could be produced on the whole surface of Ti only within 50–60 % Sr and the coatings represented a unique lamellar texture in micro/nano-scale. As Sr concentration increased, the phases of coatings were predominantly indexed to monetite and SrHPO4, which presented a highly oriented crystal alignment. With high content of Sr, monetite, instead of brushite, was deposited in the coatings. The possible mechanism of coating formation was proposed that α-SrHPO4 and α-monetite were co-deposited in the acidic phosphating solution and finally a compound of (CaxSr1-x)HPO4 was produced on surface of Ti. Results revealed that coatings formed at high degree of Sr substitution exhibited relative improved mechanical and electrochemical properties. The coatings enhanced the cell focal adhesion and proliferation of BMSCs compared with that of the bare Ti.

Magnesium or bentonite modified almond kernel biochar for phosphate adsorption from contaminated water solutions

The potential of almond kernel, physically activated by nitrogen/steam, or chemically activated by Mg2+ or bentonite and then by nitrogen/steam, to adsorb phosphate from wastewaters was evaluated. The performance of biochar was studied as a function of initial phosphate concentration, adsorbent dose, contact time and solution pH. The mechanism of adsorption was investigated by carrying out structural, chemical and mineralogical analyses of the material before and after phosphate adsorption, as well as by applying two isotherm models, simulating the experimental data. The results showed that the specific surface area increased about 260 times after activation. Adsorption of phosphate was fast within 30 min, while reached equilibrium after 12 h. For Mg2+ modified material a higher ionic strength facilitated the uptake of phosphate by the biochar up to 59%, in contrast to the bentonite modified material, where adsorption of phosphate was complete (100%) at an initial concentration of 50 mg/L, declining thereafter. Mg2+ modified material was best fitted by the Freundlich model, while bentonite modified material was best fitted by the Langmuir model. For an adsorbent dose of 2 g/L maximum phosphate adsorption capacity after Mg2+ or bentonite modification was 82 mg/g and 54 mg/g, respectively. In the case of Mg2+ modification the potential mechanisms of adsorption were surface precipitation, electrostatic attraction, chemical complexation or electron coordination between the phosphate ion and the adsorbent. For bentonite modification, chemical complexation and π-π electron coordination were the potential adsorption mechanisms.

Balancing the Anti‐Bacterial and Pro‐Osteogenic Properties of Ti‐Based Implants by Partial Conversion of ZnO Nanorods into Hybrid Zinc Phosphate Nanostructures

AbstractBacterial infection and inferior osseointegration are major complications associated with titanium (Ti) based implants. Although surface‐engineered zinc oxide (ZnO) nanorods exhibit remarkable antibacterial ability, their potential biomedical applications are hampered by their pronounced cytotoxicity. Herein, inspired by the in vivo degradation process of znic, ZnO nanorods are converted into thermodynamically more stable zinc phosphate (Zn3(PO4)2 ）through a simple hydrothermal treatment in a hydrogen phosphate solution. By adjusting the conversion ratio, the surface morphology, release of zinc ions (Zn2+), and generation of reactive oxygen species can be finely tailored to overcome the cytotoxicity of ZnO nanorods while preserving their antibacterial capability. Furthermore, an optimized amount of Zn2+ released from the ZnO/Zn3(PO4)2 hybrid coating enhances osteogenic differentiation and extracellular matrix mineralization of human bone marrow mesenchymal stem cells by reprogramming their metabolic configuration. An implant‐related infection model in rabbit femurs indicates that the hybrid ZnO/Zn3(PO4)2 coating can even promote osseointegration in the presence of pathogenic bacteria. This surface modification strategy which endows Ti‐based implants with superior anti‐bacterial and pro‐osteogenic properties holds great clinical potential for orthopedic and dental applications.

Microstructured silk fiber scaffolds with enhanced stretchability.

Despite extensive research, current methods for creating three-dimensional (3D) silk fibroin (SF) scaffolds lack control over molecular rearrangement, particularly in the formation of β-sheet nanocrystals that severely embrittle SF, as well as hierarchical fiber organization at both micro- and macroscale. Here, we introduce a fabrication process based on electrowriting of aqueous SF solutions followed by post-processing using an aqueous solution of sodium dihydrogen phosphate (NaH2PO4). This approach enables gelation of SF chains via controlled β-sheet formation and partial conservation of compliant random coil structures. Moreover, this process allows for precise architecture control in microfiber scaffolds, enabling the creation of 3D flat and tubular macro-geometries with square-based and crosshatch microarchitectures, featuring inter-fiber distances of 400 μm and ∼97% open porosity. Remarkably, the crosslinked printed structures demonstrated a balanced coexistence of β-sheet and random coil conformations, which is uncommon for organic solvent-based crosslinking methods. This synergy of printing and post-processing yielded stable scaffolds with high compliance (modulus = 0.5-15 MPa) and the ability to support elastic cyclic loading up to 20% deformation. Furthermore, the printed constructs supported in vitro adherence and growth of human renal epithelial and endothelial cells with viability above 95%. These cells formed homogeneous monolayers that aligned with the fiber direction and deposited type-IV collagen as a specific marker of healthy extracellular matrix, indicating that both cell types attach, proliferate, and organize their own microenvironment within the SF scaffolds. These findings represent a significant development in fabricating organized stable SF scaffolds with unique microfiber structures and mechanical and biological properties that make them highly promising for tissue engineering applications.

A comparison between the titanium-based and the zinc phosphate dispersion conditionings of zinc phosphate baths

ABSTRACT Phosphating is a metallic surface treatment widely used in the industrial environment as it provides greater adhesion of the paint film to the metallic substrate and greater efficiency in inhibiting corrosion. The conditioning agents in the phosphating process contribute to reducing the time to obtain the phosphate layer and favor the refinement of the formed crystals. Commercially, the most used conditioning agent is based on titanium salts, however, it is possible that other compounds may be an alternative in optimizing the industrial process. Therefore, with the aim of reducing the time and temperature of the phosphating process, this work aims to verify the performance of using the conditioning agent based on zinc phosphate in obtaining the phosphatized layer, in terms of corrosion resistance, in comparison with to the titanium-based conditioner. For this purpose, SAE 1010 carbon steel samples were degreased and sandblasted, immersed for 1 minute in the conditioning solution (titanium or zinc phosphate) and phosphated with a commercial solution of tricationic zinc phosphate at different temperatures (40 and 50°C) and immersion times (2, 3 and 4 minutes). The deposited masses of the phosphate coatings were measured and the coatings characterized by scanning electron microscopy (SEM), through electrochemical tests of open circuit potential and potentiodynamic polarization. The results showed that the greater coverage of the substrate, with the formation of denser layers, improves the anticorrosive performance of samples phosphated with both conditioners. For the titanium-based conditioner, the optimal phosphating conditions were 3 min at 50°C, while for the zinc phosphate conditioner, they were 2 min at 40°C. Therefore, for commercial use, immersion in a zinc phosphate-based conditioner is indicated, followed by phosphating for 2 min at 40°C.

High-throughput viscoelastic characterization of cells in hyperbolic microchannels.

Extensive research has demonstrated the potential of cell viscoelastic properties as intrinsic indicators of cell state, functionality, and disease. For this, several microfluidic techniques have been developed to measure cell viscoelasticity with high-throughput. However, current microchannel designs introduce complex stress distributions on cells, leading to inaccuracies in determining the stress-strain relationship and, consequently, the viscoelastic properties. Here, we introduce a novel approach using hyperbolic microchannels that enable precise measurements under a constant extensional stress and offer a straightforward stress-strain relationship, while operating at a measurement rate of up to 100 cells per second. We quantified the stresses acting in the channels using mechanical calibration particles made from polyacrylamide (PAAm) and found that the measurement buffer, a solution of methyl cellulose and phosphate buffered saline, shows strain-thickening following a power law up to 200 s-1. By measuring oil droplets with varying viscosities, we successfully detected changes in the relaxation times of the droplets and our approach could be used to get the interfacial tension and viscosity of liquid-liquid droplet systems from the same measurement. We further applied this methodology to PAAm microgel beads, demonstrating the accurate recovery of Young's moduli and the near-ideal elastic behavior of the beads. To explore the influence of altered cell viscoelasticity, we treated HL60 human leukemia cells with latrunculin B and nocodazole, resulting in clear changes in cell stiffness while relaxation times were only minimally affected. In conclusion, our approach offers a streamlined and time-efficient solution for assessing the viscoelastic properties of large cell populations and other microscale soft particles.

Aqueous alkaline phosphate facilitates the non-exchangeable deuteration of peptides and proteins.

The incorporation of deuterium into peptides and proteins holds broad applications across various fields, such as drug development and structural characterization. Nevertheless, current methods for peptide/protein deuteration often target exchangeable labile sites or require harsh conditions for stable modification. In this study, we present a late-stage approach utilizing an alkaline phosphate solution to achieve deuteration of non-exchangeable backbone sites of peptides and proteins. The specific deuteration regions are identified through ultraviolet photodissociation (UVPD) and mass spectrometry analysis. This deuteration strategy demonstrates site and structure selectivity, with a notable affinity for labeling the α-helix regions of myoglobin. The deuterium method is particularly suitable for peptides and proteins that remain stable under high pH conditions.