Sodium Hexametaphosphate Research Articles

Biocontrol of Salmonella Schwarzengrund and Escherichia coli O157:H7 planktonic and biofilm cells via combined treatment of polyvalent phage and sodium hexametaphosphate on foods and food contact surfaces

Salmonella Schwarzengrund and Escherichia coli O157:H7 are ones of foodborne pathogens that can produce biofilms and cause serious food poisoning. Bacteriophages are an emerging antibacterial strategy used to prevent foodborne pathogen contamination in the food industry. In this study, the combined antibacterial effects of the polyvalent phage PS5 and sodium hexametaphosphate (SHMP) against both pathogens were investigated to evaluate their effectiveness in food applications. The combined treatment with phage PS5 (multiplicity of infection, MOI = 10) and 1.0% SHMP inhibited the growth of S. Schwarzengrund and E. coli O157:H7, and the viable counts of both decreased by more than 2.45 log CFU/mL. In KAGOME vegetable and fruit mixed juice, the combined treatment with PS5 (MOI = 100) and 1.0% SHMP also resulted in significant pathogen inactivation at 4 °C after 24 h. PS5 (1010 PFU/mL) and 1.0% SHMP showed stronger synergistic effects on biofilm formation and the removal of established biofilms on polystyrene plates. Additionally, we evaluated their combined effects on reducing the biofilms of S. Schwarzengrund and E. coli O157:H7 on glass tubes and cabbage leaves at 4 °C. These findings indicate the utility of this approach in the biocontrol of the planktonic and biofilm cells of S. Schwarzengrund and E. coli O157:H7 on foods and food contact surfaces.

Fast and effective adsorption of Ce3+ by phosphate-functionalized ZIF-67-derived layered double hydroxides

In this experiment, phosphate (sodium hexametaphosphate) was used as an intercalation modifier and ZIF-67 as a precursor mixed with Al(NO3)3·9H2O Nanolayered double hydroxides P-Co-Al-LDH with hexametaphosphate group intercalation were prepared in a hydrothermal environment and characterized by SEM, FT-IR, XRD, TGA, SEM and XPS. The adsorption performance of P-Co-Al-LDH and control Co-Al-LDH on Ce3+ under different adsorption conditions was firstly investigated by optimization experiments. It was determined that the best adsorption effect of P-Co-Al-LDH was achieved at pH=6, and the fast equilibrium adsorption state was achieved within 30 min, with the adsorption amount reaching 220.98 mg/g and the adsorption efficiency reaching 72.66%. In addition, kinetic, isothermal adsorption and thermodynamic modeling explored the adsorption mechanism of Ce3 + by nanodiamond P-Co-Al-LDH mainly the complexation of functional groups in sodium hexametaphosphate with metal ions greatly improved the adsorption performance. Several regeneration experiments were carried out to evaluate the stability and reusability of the adsorbent. After three cycles of adsorption, the adsorption efficiency was still maintained at 83.26%.

Investigation of serpentine entrainment reduction in pentlandite flotation using eco-friendly sodium alginate in suspension dispersion systems

Magnesium silicates pose severe environmental issues in hydrometallurgical processes. Copper-nickel sulfide ores are the primary source for nickel production, but their increasingly complex properties make separation difficult, causing slimy magnesium silicate minerals to be entrained into the concentrate with the foam, leading to magnesium contamination. Studies have found that sodium alginate (SA), as an environmentally friendly polymer reagent, can effectively inhibit serpentine. This work investigates the effect of SA on the flotation behavior of pentlandite and serpentine in a sodium hexametaphosphate (SHMP) system. Sedimentation tests show that only a low dosage of SA can effectively settle serpentine, while excessive SA disperses serpentine. Flotation tests indicate that SA can further increase the difference in recovery rates between pentlandite and serpentine based on SHMP. Results from artificial mixed ore tests demonstrate that the recovery rate of serpentine decreases from 51.22% to 37.37% with the addition of SA, with minimal impact on the recovery rate of pentlandite. To explain the impact of the SA adsorption process on the mineral states, the following tests and analyses were conducted: TOC and QCM-D results indicate that SA mainly adsorbs onto serpentine, forming rigid adsorption at low dosages and flexible adsorption at high dosages. Zeta potential tests reveal changes in the surface potential of the minerals, explaining the transition from electrostatic attraction to electrostatic repulsion between pentlandite and serpentine. FTIR and XPS results show that SA chemically reacts with the Mg and Si sites on the serpentine surface through its -COO- groups. In summary, in the SHMP system, the use of gel adsorption and the chemical interaction of SA to coagulate and depress serpentine reduces its entrainment into the concentrate, achieving efficient separation of pentlandite and serpentine. However, high dosages of SA do not yield satisfactory results.

Influence of SHMP Concentration on Rutile Flotation in BHA System: Guiding the Separation of Rutile and Hornblende.

Sodium hexametaphosphate (SHMP) is a common depressant used in rutile flotation, especially for silicate gangue minerals such as amphibole. However, the experiment found that in the benzyl hydroxamic acid (BHA) system, SHMP of small concentrations affected the flotation recovery of rutile. In this work, the influence mechanism of SHMP concentration on the flotation of rutile in the BHA system was studied by flotation test, adsorption capacity determination, ζ potential determination, infrared spectrum analysis, and X-ray photoelectron spectroscopy (XPS) analysis. The test results show that in the BHA system, SHMP chemically adsorbs on the rutile surface, hindering the effect of BHA on the rutile surface, and hydrolyzes in the pulp to form hydrophilic colloids. When the concentration of BHA is 40 mg/L and that of SHMP is 6 mg/L, the effect of SHMP is the most obvious. However, with the increase of SHMP concentration to 8-10 mg/L, its effect on the recovery of rutile became very weak. When the concentration of SHMP is lower than 6 mg/L, the SHMP anion-metaphosphate ion (SHMP-) interacts with the hydrophilic colloidal particles on the surface of rutile, which affects the combination of BHA and the active sites on the surface of rutile, thus affecting the recovery of rutile. When the concentration of SHMP continues to increase, the SHMP- adsorbed on the rutile surface is removed from the rutile surface due to the charge repulsion and the competitive adsorption of BHA.

Evaluation of the Preservation of Chitinozoans in a Case Study of the Katian?—Hirnantian Succession, Eastern Precordillera of Argentina

The poor preservation state of chitinozoans recovered from samples of the La Pola (Sandbian–Katian) and Don Braulio formations (Hirnantian-Llandovery), after being processed with standard methods, required significant modifications in processing. The sodium hexametaphosphate technique was used to avoid invasive mechanical procedures. Hence, more complete chitinozoans that preserved original features produced by biological, mechanical, and chemical degradation appeared. The processes that affected the good preservation of the chitinozoan exine are associated with factors inherent to the sedimentary environment, and biological and geological taphonomic effects that occurred in different regions of the Precordillera, added to the important associated tectonic activity. The thermal alteration was also an important factor in the fragile and brittle condition of the organic matter recovered. This transcends the preservation-processing technique relationship to be used. The results obtained from non-standard processing contribute to the paleoenvironmental interpretation of the Pola and Don Braulio successions, which are still widely discussed, and the determination of the most accurate age of the La Pola Formation. The latter will allow us to propose a biostratigraphic correlation between chitinozoan zones and graptolite zones, given the presence of both groups in the succession studied here, and to establish correlations with other successions in the Precordillera and elsewhere.

Assessing the role of seawater in the flotation behavior of chalcopyrite and sphalerite

ABSTRACT In seawater flotation, some chemical properties of seawater affect the flotation separation of chalcopyrite and sphalerite. Using seawater instead of fresh water to separate copper – zinc can save fresh water resources and reduce lime consumption, which has broad prospects in terms of economic and environmental protection. In this paper, the flotation separation behavior of chalcopyrite and sphalerite in seawater was tested and the mechanism was analyzed. As a contrast, the copper grade of concentrate in seawater flotation declined from 23.7% to 22.6%. Meanwhile, the recovery of chalcopyrite declined from 66.2% to 42.8% and the SI value declined from 2.210 to 1.599. With the addition of sodium hexametaphosphate, sodium silicate and EDTA, the SI value increased from 1.599 to 2.176, 2.238 and 2.096, respectively. Nevertheless, when EDTA was excessive, the SI value was only 1.998. This indicated that excessive EDTA is unfavorable to flotation separation of chalcopyrite from sphalerite. Wettability analysis, zeta potential analysis, X-ray photoelectron spectroscopy, Fourier transform infrared spectroscopy, density functional theory calculation and E-DLVO calculation verified the flotation separation behavior and revealed the mechanism.

The Effect of Sodium Hexametaphosphate on the Dispersion and Polishing Performance of Lanthanum-Cerium-Based Slurry.

A lanthanum-cerium-based abrasive composed of CeO2, LaOF, and LaF3 was commercially obtained. The effect of sodium hexametaphosphate (SHMP) on powder dispersion behavior was systematically investigated using the combined techniques of liquid contact angle, turbidity, zeta potential (ZP), scanning electron microscopy (SEM), powder X-ray diffraction (XRD) combined with Rietveld refinements, X-ray photoelectron spectroscopy (XPS), and polishing tests. The results indicated that the addition of 0.5 wt.% SHMP dispersant to the 5 wt.% lanthanum-cerium-based slurry produced the most stable suspension with a high turbidity of 2715 NTU and a low wetting angle of 45°. The as-obtained slurry displayed good surface polishing quality for K9 glass, with low surface roughness (Ra) of 0.642 and 0.515 nm (in the range of 979 × 979 μm2) at pH = 6 and 11, respectively, which corresponds to the fact that it has local maximum absolute values of ZP at these two pH values. SEM images demonstrated that after appropriate grafting of SHMP, the particle aggregation was reduced and the slurry's dispersion stability was improved. In addition, the dispersion mechanism was explained based on the principle of complexation reaction, which reveals that the dispersant SHMP can increase the interparticle steric hindrance and electrostatic repulsions. In an acidic environment, steric hindrance dominates, while electrostatic repulsion prevails under alkaline conditions. As expected, this polishing slurry may find potential applications in manufacturing optical devices and integrated circuits.

Modifying Cassava Starch via Extrusion with Phosphate, Erythorbate and Nitrite: Phosphorylation, Hydrolysis and Plasticization.

Extrusion processing of plasticized cassava starch, a prominent industrial crop, with chemical additives offers a thermo-mechanical approach to modify starch structures through physical and chemical interactions. This research investigates the interaction and morphology of thermoplastic cassava starch (TPS) blended with tetrasodium pyrophosphate (Na4P2O7), sodium tripolyphosphate (Na5P3O10), sodium hexametaphosphate (Na6(PO3)6), sodium erythorbate (C6H7O6Na), and sodium nitrite (NaNO2) via twin-screw extrusion. The effects of these additives on the chemical structure, thermal profile, water absorption, and solubility of the TPS were examined. The high temperature and shearing forces within the extruder disrupted hydrogen bonding at α-(1-4) and α-(1-6) glycosidic linkages within anhydroglucose units. Na4P2O7, Na5P3O10 and Na6(PO3)6 induced starch phosphorylation, while 1H NMR and ATR-FTIR analyses revealed that C6H7O6Na and NaNO2 caused starch hydrolysis. These additives hindered starch recrystallization, resulting in higher amorphous fractions that subsequently influenced the thermal properties and stability of the extruded TPS. Furthermore, the type and content of the added modifier influenced the water absorption and solubility of the TPS due to varying levels of interaction. These modified starch materials exhibited enhanced antimicrobial properties against Escherichia coli and Staphylococcus aureus in polyester blends fabricated via extrusion, with nitrite demonstrating the most potent antimicrobial efficacy. These findings suggest that starch modification via either phosphorylation or acid hydrolysis impacts the thermal properties, morphology, and hydrophilicity of extruded cassava TPS.

Enhancing lepidolite flotation efficiency with the novel LCJ collector: comparative analysis and mechanistic insights in Jiangxi Province’s lepidolite resources

ABSTRACT This study evaluates the flotation performance of a novel combination collector, LCJ, on lepidolite from Jiangxi Province, China. A comparative analysis with the on-site collector EO demonstrates an economically efficient separation scheme for lepidolite. Results show that LCJ outperforms EO in capturing lepidolite. Employing 400 g/t sodium hexametaphosphate as an inhibitor and 290 g/t LCJ as a collector, a flotation process with one rougher, two cleaner, and two scavenger stages achieves a lepidolite concentrate with a Li2O grade of 2.10% and a recovery of 78.62%. LCJ also enhances foamability within conventional air-inflation ranges. Infrared testing, Zeta potential analysis, and contact angle measurements indicate similar organic adsorption on the lepidolite surface for both collectors. However, LCJ significantly influences the Zeta potential, increasing hydrophobicity. These findings confirm LCJ as an efficient and selective collector for lepidolite flotation, with promising application prospects.

Evaluation of rheo-viscoelasticity of magnesium-silicate-hydrate mixes incorporating different superplasticizers

This study investigated rheo-viscoelastic behaviors of MgO-SiO2 pastes with three phosphate additives (sodium hexametaphosphate (SHMP), sodium trimetaphosphate (STMP), and sodium orthophosphate (SOP)) as superplasticizers. Static yield stress, dynamic yield stress, median differential viscosity, thixotropic loop area, structural recovery rate, and non-destructive structural build-up were analyzed. Furthermore, assessment of hydration and particle dispersion stability was facilitated by employing isothermal calorimetry, XRD, DTG, and zeta potential techniques. SHMP significantly decreased the static and dynamic rheology, thixotropy, and viscoelastic evolution. Samples incorporating 2 wt% SOP exhibited enhanced rheological parameters, particularly static yield stress, owing to increased brucite formation and a denser microstructure in the fresh paste. Adsorption of phosphate additives on MgO surfaces inhibited formation of brucite and improved interparticle electrostatic repulsion, thereby increasing suspension stability. High-efficiency adsorption of SHMP on MgO surfaces, coupled with the retardation of brucite nucleation-and-growth, and enhancement in suspension stability, greatly restrained the rheo-viscoelastic evolution of MgO-SiO2 system.

Experimental study on a direct-expansion micro-channel PV/T evaporator using water-ZnO nanofluid as the spectral beam splitter

Introducing nanofluid (NF) as the spectral beam splitter (SBS) in photovoltaic/thermal (PV/T) evaporators can significantly enhance their performance and energy flexibility. In this study, a novel direct-expansion micro-channel evaporator using water-ZnO nanofluid as SBS (i.e., NF-MC-PV/T evaporator) was manufactured. Particularly, the stability of low-viscosity water-ZnO nanofluid was first optimized and natural convection within the NF-MC-PV/T evaporator was directly formed. Further, a direct-expansion heat pump system based on the NF-MC-PV/T evaporator was developed and tested. According to the findings, adding sodium hexametaphosphate as a dispersant with the dispersion ratio of 1:5 and ultrasonic treatment for 1.5 h can achieve the optimal stability of water-ZnO nanofluid. The nanofluid's natural convection can reduce the evaporator's operating temperature and improve the PV module's temperature distribution uniformity. Specifically, the NF-MC-PV/T evaporator's operating temperature was lower than the environment temperature and a pure PV module. Besides, the PV module's temperature distribution was uniform in the direction perpendicular to the refrigerant flow with a max temperature gradient of only 4.59 °C. The typical photothermal efficiency of the NF-MC-PV/T evaporator reached 102.55 % while the heat loss coefficient was only 4.37. Moreover, the average photothermal efficiency, photovoltaic efficiency, and COP of the system were 103.58 %, 12.03 %, and 5.09, respectively.

Influence of various ion chelators on mechanical, transport and microstructure properties of cement-based materials

Influence mechanism of various ion chelators on the mechanical, transport, and microstructure properties of cement-based materials was explored. The ion chelators included pentasodium diethylenetriamine pentaacetate, tetrasodium ethylenediaminetetraacetate, sodium hexametaphosphate and tetrasodium glutamate diacetate, with a dosage of 1% of the cement mass. The effect of ion chelators on the mechanical, transport, and pore structure properties was evaluated by compressive, sorptivity, and mercury intrusion porosimetry (MIP) tests. The composition and microstructure of hydration products were studied by scanning electron microscope (SEM) and X-ray diffractometer (XRD). Test results indicated that four ion chelators reduced the mechanical and transport properties, and increased the porosity of specimens at 3 d and 7 d. And four ion chelators improved the mechanical and transport properties, and reduced porosity at 28 d and 56 d. The fundamental reason for the differences in the basic properties of cement-based materials caused by the types of ion chelators is that different ion chelators possess various calcium chelating capacities and stability of calcium complexes, which leads to different impact on the complexation substitution reaction process. Moreover, compared to the stability of calcium complexes, the influence of calcium chelating ability on the basic properties of specimens is more significant in the early curing ages.

Optimization of Na2SO4•10H2O composites for cold storage by D-optimal mixture design

This study delved into the creation of a composite phase-change material (PCM), named SBNSC, for potential application in cold storage air-conditioning systems (8–16°C). The composite PCM was formulated using sodium sulfate decahydrate (Na2SO4·10H2O) as the primary PCM, borax as a nucleating agent, ammonium chloride (NH4Cl) as a temperature control additive, sodium hexametaphosphate as a crystal modifier and carboxymethylcellulose as a thickening agent. The D-optimal mixture design was employed to optimize the composition, and this resulted in the identification of an optimal formulation characterized by the most desirable properties. The thermal properties were evaluated using differential scanning calorimetry and revealed a phase-change temperature of 15.40°C. X-ray diffraction analysis confirmed the crystalline nature of the composite PCM. After 100 cooling and heating cycles, the crystallization temperature was 9.50°C, the melting temperature was 15.50°C and the supercooling degree was 0.70°C. The enthalpy values showed an 11.22% decrease, indicating reliable thermal performance. The study concluded that the optimal formulation (SBNSC) exhibits commendable thermophysical properties, demonstrating its potential for effective application in phase-change cold storage air-conditioning systems.

Simple incorporation and calcination of Zn-Al LDH during PEO processing in near-neutral pH solutions

Plasma electrolytic oxidation (PEO) process was employed for preparing oxide coatings on AA2024 aluminum alloy in solutions containing Zn-Al layered double hydroxide (LDH) particles. Sodium hexametaphosphate aqueous solution was selected as the standard solution, based on its almost neutral pH value considered as important for the LDH stability. Different additives to the standard solution were examined including 2-mecaptobenzothiazole (MBT) and different Zn-Al LDH compounds. The formed coatings underwent characterization regarding their morphology, chemical and phase composition, as well as assessment of their photocatalytic and corrosion protection efficiency. Coating thickening and compactness evolution were noted for all coatings with LDH additions to the standard solution. Obtained coatings are well-crystallized featuring γ-Al2O3 and two Zn-containing crystalline phases, namely ZnO and NaZnPO4, originating mainly from the LDH addition to the solution. PEO coatings obtained in this study demonstrated very reasonable photocatalytic activity for immobilized photocatalyst, reaching 51 % after 6 h under UV irradiation. The inclusion of Zn-Al LDH substantially boosted the impedance modules at low frequencies by two orders of magnitude compared to bare AA2024 alloy when exposed to a 3.5 % NaCl solution.

Experimental and theoretical investigations into the surface chemical properties and separation of serpentine from quartz using xanthomonas campestris as a selective flocculant

Separation of fine serpentine (SPT) from quartz (QZ) both of d80 close to 20 µm using an eco-friendly microbial exo-polysaccharide, xanthomonas campestris (XCT), as a selective flocculant for SPT was conducted experimentally and substantiated theoretically. The adsorption of XCT onto SPT was observed to decrease with increase in pH, whereas that of QZ was nearly nil beyond pH 2.1. Zeta potential of SPT in presence of XCT decreased with increase in pH further attesting to the adsorption and anionicity of XCT. The FTIR studies confirmed the interaction of XCT with SPT in presence of sodium hexametaphosphate. The nature of intermolecular interactions present in complexes formed on SPT surface was revealed by quantum theory of atoms in molecules to be non-covalent. The electron density difference plot conducted on formed complexes indicated that electrons drifted from XCT to the surface of SPT. Selective flocculation SPT-QZ (1:1) mixture conducted at pH 6 and pH 7.5 in presence of 4 mg/L and 2 mg/L of sodium hexametaphosphate coupled with 100 mg/L of XCT yielded separation efficiency and selectivity ratio of 96.5 % and 71.2, respectively, after three desliming stages. Therefore, XCT is a potential selective flocculant for serpentine.

Selective aggregation of hematite from quartz using charged polyacrylamides: In-situ sizing

Recovering fine valuable material has been a significant challenge in minerals processing. This primarily stems from insufficient collision opportunities between fine particles and bubbles, specifically when utilising traditional recovery methods such as froth flotation. This research endeavours to address this challenge by exploring the use of various commercially available, high molecular weight polymers- specifically polyacrylamide (PAM)- to selectively aggregate hematite from quartz. Investigation of the conditions in which selective aggregation of hematite over quartz occurs, with the goal to achieve aggregate sizes of between 20 and 150 μm, were undertaken. Targeting this size range ensure that conditions are optimised for future use in conventional mechanical flotation cells as an efficient mineral recovery method. The study investigates the selectivity of charged PAM towards hematite and quartz at pH 10, using adsorption studies. Anionic PAM demonstrates a preference for hematite, with a range of charge density studies, highlighting stronger adsorption capacity with lower charge density polymers. Using BlazeMetrics probe technology for in-situ sizing and imaging, it was observed that conditioning 50–300 g APAM per t of hematite resulted in aggregates in the range of 30–230 μm after 5 min. Interestingly, the charge density of APAM does not markedly affect the size of the hematite aggregates, although altering the charge density of the polymer impacts the selectivity towards quartz. Additionally, cationic PAM results in the simultaneous aggregation of both hematite and quartz, not demonstrating selectivity. To mitigate heterocoagulation between minerals, a common dispersant, sodium hexametaphosphate (SHMP), was employed, which notably prevents quartz aggregation. Separation of aggregated hematite from quartz by sedimentation was only slightly effective with the majority of quartz settling with the hematite. Adding up to 1000 g of dispersant per t of hematite reduced the amount of quartz in the sediment bed by 23 %. The dispersant increased the magnitude of the negative zeta potential of the two minerals, particularly hematite, lowering heterocoagulation and improving effectiveness of hematite flocculation.

The optimizing role of regulators in separation of lead − copper in seawater and analysis of related mechanism

Using seawater for mineral flotation conserves fresh water resources and offers significant environmental and economic benefits. However, the adverse effect of seawater restricts its application in mineral flotation. The regulators can eliminate the adverse effect caused by seawater during flotation separation of lead and copper. In this paper, the flotation separation of galena and chalcopyrite in seawater was tested. Compared with those in deionized water, the lead grade of concentrate in seawater flotation declined from 50.10% to 48.90%. Meanwhile, the recovery of galena declined from 74.33% to 60.58% and the SI value declined from 1.565 to 1.324. With the addition of SHMP (sodium hexametaphosphate), SS (sodium silicate) and EDTA (ethylenediamine tetraacetic acid), the SI value increased from 1.324 to 1.923, 2.002 and 1.939, respectively. Noteworthy, when EDTA was excessive, the grade of Pb was 60.80%, the recovery of galena was 60.86% and the SI value was 2.113. X-ray photoelectron spectroscopy, Fourier transform infrared spectroscopy, Atomic force microscopy, Density functional theory calculation and E-DLVO calculation verified the micro-flotation results and revealed the mechanism of action.

Soluble Salts in Processed Cheese Prepared with Citrate- and Phosphate-Based Calcium Sequestering Salts.

In this study, the protein and salts distribution (Ca, P, Na and Mg) in processed cheese (PC) samples prepared with 180 or 360 mEq/kg of the calcium sequestering salts (CSS) disodium phosphate (DSP), disodium pyrophosphate (DSPP), sodium hexametaphosphate (SHMP) and trisodium citrate (TSC) was studied. For this purpose, a water-soluble extract (WSE) of PC samples was prepared. All PC samples contained 45-46% moisture, 26-27% fat and 20-21% protein and had a pH of 5.2 or 5.7. Ultracentrifugation slightly reduced the protein content of the WSE of PC, indicating that most protein in the WSE was non-sedimentable. At equal concentration of CSS, the protein content of the WSE was higher for PC at pH 5.7 compared to PC at pH 5.2. Approximately 55-85% of the Ca and P in the WSE of samples was 10 kDa-permeable for PC prepared with DSPP and SHMP. This suggests that the formation of non-permeable Ca-polyphosphate-casein complexes. For PC prepared with TSC, >90% of Ca in the WSE was 10 kDa-permeable, indicating that micellar disruption arises from sequestration of micellar Ca. These results indicate that the WSE method is an appropriate method to understand how salts present in PC are distributed. However, the WSE and ultracentrifugal supernatant of the WSE can include both soluble and protein-associated salts. Therefore, determining levels of salts in 10 kDa permeate of ultracentrifugal supernatant of the WSE is most appropriate.

Study on filament deflection in lattice porous structures fabricated through direct ink writing

AbstractDirect ink writing (DIW) technology supersedes traditional mold‐based forming methods, significantly enhancing the fabrication of personalized and customized products with complex structures. This technology particularly excels in achieving precise control over the porosity of porous constructs. This study employs inorganic Al2O3 as raw material, sodium hexametaphosphate as dispersing agent, and inorganic SiO2 micropowder as binding medium to fabricate lattice porous structures. One challenge encountered is the viscoelastic behavior of the extruded filament. When spanning the unsupported segments of the lower layer, the upper extruded filaments are susceptible to deflection or collapse, adversely affecting the porosity and dimensional fidelity of the final specimens. Experimental results revealed that a larger span and smaller modulus will cause the extruded filament to be more prone to deformation at the midpoint. The introduction of 2 wt% polyethylene glycol as a plasticizer mitigates this issue, ensuring nondeflection of the extruded filaments at a span of 6 mm. The deflection model for the extruded filament about span and modulus identifies the minimum modulus necessary to prevent or minimize deflection under given spans, which closely approximates our experimental findings, offering a valuable framework for guiding the production of high‐precision, porosity‐controlled porous structures.

Diaminonaphthalene functionalized LUS-1 as a fluorescence probe for simultaneous detection of Hg2+ and Fe3+ in Vetiver grass and Spinach

One of the important problems in the environment is heavy metal pollution, and fluorescence is one of the best methods for their detection due to its sensitivity, selectivity, and relatively rapid and easy operation. In this study, 1,8-diaminonaphthalene functionalized super-stable mesoporous silica (DAN-LUS-1) was synthesized and used as a fluorescence probe to identify Hg2+ and Fe3+ in food samples. The TGA and FT-IR spectra illustrated that 1,8-diaminonaphthalene was grafted into LUS-1. XRD patterns verified that the LUS-1 and functionalized mesoporous silica have a hexagonal symmetrical array of nano-channels. SEM images showed that the rod-like morphology of LUS-1 was preserved in DAN-LUS-1. Also, surface area and pore diameter decreased from 824 m2 g⁻1 and 3.61 nm for the pure LUS-1 to 748 m2 g⁻1 and 3.43 nm for the DAN-LUS-1, as determined by N₂ adsorption–desorption isotherms. This reduction demonstrated that 1,8-diaminonaphthalene immobilized into the pore of LUS-1. The DAN-LUS-1 fluorescence properties as a chemical sensor were studied with a 340/407 nm excitation/emission wavelength that was quenched by Hg2+ and Fe3+ ions. Hg2+ and Fe3+ were quantified using the fluorescence response in the working range 8.25–13.79 × 10–6 and 3.84–10.71 × 10–6 mol/L, with detection limits of 8.5 × 10–8 M and 1.3 × 10–7 M, respectively. Hg2+ and Fe3+ were measured in vetiver grass and spinach. Since the Fe3+ quenching can move in the opposite direction with sodium hexametaphosphate (SHMP) as a hiding compound for Fe3+, consequently, the circuit logic system was established with Fe3+, Hg2+, and SHMP as inputs and the fluorescent quench as the output.