Search Results (43)

An integrated process scheme is developed for valorizing filtered liquid digestates (FLD) from an industrial anaerobic digestion (AD) plant treating dairy-processing effluents with relatively low nutrient concentrations. The process scheme involves FLD treatment by nanofiltration (NF) membranes, followed by struvite recovery from the NF-retentate. An NF pilot unit (designed for this purpose) is combined with a state-of-the-art NF/RO process simulator. Validation of simulator results with pilot data enables reliable predictions required for scaling up NF systems. The NF permeate meets the standards for restricted irrigation and/or reuse. Considering the significant nutrient concentrations in the NF retentate (i.e., ~500 mg/L NH4-N, ~230 mg/L PO4-P), struvite recovery/precipitation is investigated, including determination of near-optimal processing conditions. Maximum removal of nutrients, through production of struvite-rich precipitate, is obtained at a molar ratio of NH₄:Mg:PO₄ = 1:1.5:1.5 and pH = 10 in the treated stream, attained through the addition of Κ₂HPO₄, ΜgCl₂·6H₂O, and NaOH. Furthermore, almost complete struvite precipitation is achieved within ~30 min, whereas precipitate/solid drying at modest/ambient temperature is appropriate to avoid struvite degradation. Under the aforementioned conditions, a significant amount of dry precipitate is obtained, i.e., ~12 g dry mass per L of treated retentate, including crystalline struvite. The approach taken and the obtained positive results provide a firm basis for further development of this integrated process scheme towards sustainable large-scale applications. Full article

The content of modified materials in multicomponent gel phase change materials directly affects their performance characteristics. To investigate the influence of different contents of modified materials on the performance features of Na₂HPO₄·12H₂O-based multicomponent Gel Phase Change Materials, four single factors (Na₂SiO₃·9H₂O, C₃₅H₄₉O₂₉, KCl, and nano-α-Fe₂O₃) and their interactions were selected as influencing factors. Using the Taguchi method with an L₂₇(3¹³) orthogonal array, multi-step melt–blending experiments were conducted to prepare a novel multi-component phase change material. The characteristics of the new multi-component phase change material, including supercooling degree (ΔT), phase change temperature (T_m), latent heat of phase change (ΔH_m), and cooling time (CT), were obtained. In addition, characterization techniques such as DSC, SEM, FT-IR, and XRD were employed to analyze its thermal properties, microscopic morphology, chemical stability, and crystal structure. Based on the experimental results, the signal-to-noise ratio (S/N) was used to rank the influence of each factor on the quality characteristics, and the p-value from analysis of variance (ANOVA) was employed to evaluate the significance of each factor on the performance characteristics. Then, the effects of each significant factor on the characteristics of the multiple gel phase change materials were analyzed in detail, and the optimal mixing ratio of the new multiple gel phase change materials was selected. The results showed that Na₂SiO₃·9H₂O, KCl, and α-Fe₂O₃ were the most critical process parameters. This research work enriches the selection of composite gel phase change materials for solar greenhouses and provides guidance for the selection of different modified material contents using Na₂HPO₄·12H₂O as the starting material. Full article

In this study, fumed silica (FS) was used as a support material and infused with the hydrated salt sodium hydrogen phosphate dodecahydrate (DHPD) to create shape-stabilized constant phase change materials (CPCMs). These CPCMs were integrated into a polyurethane matrix as a functional filler, resulting in low-exothermic polyurethane composite foams (CPCM-RPUFs) that demonstrate thermoregulation and flame-retardant properties. Recent findings show that CPCM-RPUF excels in thermal stability compared to pure polyurethane, with a melt phase transition enthalpy of 115.8 J/g. The use of fumed silica allows for the encapsulation of hydrated salts up to 87%, ensuring the structural integrity of the vesicles. As FS content in CPCMs increased, the internal temperature of the composite foam significantly decreased, showing excellent thermal regulation. Thermogravimetric analysis showed that the synergistic effect of DHPD and FS improved the thermal stability and flame retardancy of the composites. By monitoring the internal and surface temperature changes in the foam, it was verified that CPCMs can effectively alleviate heat accumulation during the curing process and reduce the core temperature (56.9 °C) and surface warming rate, thus realizing the thermal buffering effect. With the increase in FS content in CPCMs, the compressive strength of CPCM-RPUF can be maintained or even enhanced. This study provides a theoretical basis and technical support for the development of polyurethane composite foams with integrated thermal regulation and flame-retardant properties, which can have broad application prospects in the fields of building energy conservation, energy storage equipment, and thermal mine insulation. Full article

This paper presents a new account of the mineralogy of the bat guano deposit in Gaura cu Muscă Cave, Locvei Mountains, Romania. The cave, which, in its main proportion, is a wet, “live” cave, has a dry portion hosting guano. Biogenic leucophosphite is one of the main compounds of the fossil bat guano association in the cave, where it occurs together with hydroxylapatite, taranakite, ardealite, calcite, quartz and illite (the 2M1 polytype). The mineral species from the cave were characterized by optical methods, scanning electron microscopy, wet-chemical analysis, X-ray powder diffraction, Fourier-transform infrared and inductively coupled plasma – atomic emission spectrometry. The crystal-chemical formula of leucophosphite from Gaura cu Muscă is [K_0.978Na_0.003(NH₄)_0.014](Al_0.085Fe_1.903Mg_0.001Mn_0.006)(PO₄)₂(OH)_0.973·2H₂O. The cell parameters calculated for the same sample are a = 9.813(6) Å, b = 9.749(6) Å, c = 9.631(9) Å and β = 102.30(2)°. The infrared spectrum affords the presence of (PO₄)³⁻, (HPO₄)²⁻, (NH₄)⁺ and (OH)⁻ ions, together with H₂O molecules. The band multiplicity on the IR absorption spectrum suggests that the phosphate groups in the structure have C_s punctual symmetry. The host deposit was formed under extremely “dry” conditions that favored a sharp decrease in the pH of solutions derived from the guano mass. Full article

Coal mining frequently sees explosions caused by methane/coal dust mixtures, resulting in significant harm to people and property damage. This study utilized the Hartmann pipe experiment to investigate the inhibition mechanisms of ultrafine water mist (UWM) containing phosphorus-based sodium inhibitors (sodium dihydrogen phosphate (NaH₂PO₄) and sodium phytate (C₆H₆Na₁₂O₂₄P₆)) on methane/coal dust hybrid explosions. The results indicate that UWM containing NaH₂PO₄ and C₆H₆Na₁₂O₂₄P₆ significantly reduces flame propagation velocity, flame height, and flame temperature, thereby effectively inhibiting the development of methane/coal dust hybrid explosion flames. UWM containing C₆H₆Na₁₂O₂₄P₆ exhibited superior inhibition performance, reducing the flame temperature to 157.6 °C, the peak flame propagation velocity by 2.26 m/s, and the flame height by 5.66 mm. The inhibition mechanism of UWM containing phosphorus-based sodium inhibitors primarily involves physical heat absorption and chemical inhibition. The evaporation of UWM absorbs heat, thereby reducing the temperature in the reaction zone. Simultaneously, it generates a large amount of water vapor, which dilutes the fuel concentration per unit volume and reduces the collision frequency between fuel molecules and oxygen. The active free radicals (such as sodium oxygen radical (NaO), metaphosphoric acid (HPO₂), HOPO (peroxyphosphate radical), etc.) produced by the decomposition of NaH₂PO₄ and C₆H₆Na₁₂O₂₄P₆ react with free radicals (O, H, and OH), effectively reducing the concentration of free radicals, interrupting the chain reaction, and weakening the explosive severity. The decomposition products of the phosphorus-sodium components increase the heat capacity of the combustion products, dilute and isolate the combustion zone, and further reduce the explosive severity. These findings provide significant scientific and engineering support for the safe management of coal mines. Full article

At present, contamination due to toxic metals is a global concern. The management of problems caused by heavy metals relies on stabilization/solidification, which is the most effective technique for the control of metal pollution in soil. This study examined the immobilization efficiency of various phosphate-based binders (Na₃PO₄, Na₂HPO₄, NaH₂PO₄), in addition to ordinary Portland cement (OPC), MgO, and CaO, for the stabilization of multi-metal-contaminated soils. Moreover, this study focused on the leachability of copper, nickel, zinc, lead, cadmium, and manganese (Cu, Ni, Zn, Pb, Cd, Mn, respectively) over different time periods and with different concentrations. Batch leaching experiments were conducted to determine the leaching ratios and percentages of the various metal concentrations, along with measuring the pH values of the leachates. Our results indicate that the use of OPC was validated due to its superior immobilization performance across all metals present in the soil, but particularly with regard to metals in high concentrations. This was due to the formation of stable hydroxides and the high pH values, which assisted in abating the metals’ solubility. Additionally, phosphate-based binders, despite being environmentally favorable, were found to be less effective, particularly for Pb and Cu, and the leaching results exceeded non-hazardous waste limits. MgO showed reasonable immobilization results but was less effective compared to OPC; on the other hand, CaO exhibited increased leaching over time. Therefore, the present research serves primarily to highlight that OPC is more suitable for soil remediation at industrial sites and in the construction of infrastructure. Meanwhile, phosphate-based binders are shown to be more appropriate for eco-friendly, non-load-bearing applications. Full article

In this paper, a morphologically stable composite phase change material (CPCM) suitable for use in the field of building energy conservation was developed using Na₂HPO₄∙12H₂O (DHPD) as the phase change material, Na₂SiO₃∙9H₂O (SSNH) as the nucleating agent, and silica aerogel (SA) as the carrier. The results showed that the incorporation of 25 wt% SA resulted in the as-prepared DHPD-SSNH/SA CPCM with a phase change temperature of 30.4 °C, an enthalpy of 163.4 J/g, and a low supercooling degree of 1.3 °C, which also solved the corrosion problem of reinforcing bars caused by the hydrated salt PCM. Meanwhile, DHPD-SSNH/SA CPCM had good shape stability and low thermal conductivity (0.1507 W/(m·K)). The phase change temperature was basically unchanged, and the enthalpy only decreased by 4.8% after 200 cold-heat cycles. In addition, the thermal performance evaluation of CPCM showed that the indoor thermal comfort time of the testing system loaded with PCM board accounted for 50.75%, which was 43.38% higher than that of the one without PCM board (7.37%). The results suggest that the obtained CPCM had a good energy saving effect and great potential in the field of building energy conservation. Full article

Electrogenerated hydrophilic carbon (EHC) nanomaterials emerge as a highly attractive option for mimicking the activity of the superoxide dismutase enzyme (SOD) due to their exceptional water solubility and electron-transfer reversibility. Motivated by these properties, the EHC nanomaterials were utilized to assess the effect of ionic strength on the SOD-like activity. Superoxide anion radicals (O₂^•−) were generated using the hypoxanthine–xanthine oxidase system, with nitro blue tetrazolium chloride serving as the detecting system. A significant boost in the SOD-like activity was found via the addition of an electrolyte to the as-prepared nanomaterial solution. The effect of the electrolyte cation (Na⁺ and K⁺), as well as its counterion (Cl⁻, CH₃COO⁻, and H₂PO₄⁻/HPO₄²⁻) were analyzed. Based on these studies, a new formulation for the preparation of the carbon-based nanomaterial was established. It was demonstrated that the SOD-like activity follows an enzyme-type catalytic activity rather than the stoichiometric scavenging of the superoxide anion radical. It was concluded that 12.71 µg/mL of the EHC nanomaterial exhibits catalytic activity comparable to 15.46 µg/mL of the native Cu/Zn-SOD enzyme. This study provides a starting point for the development of a new nanotool to fight the oxidative stress associated with pathophysiological conditions where SOD activity is depleted. Full article

This work aimed to identify the influence of pH, molarity, w/v fraction, extraction time, agitation, and either a sodium (Na₂HPO₄·7H₂O-NaH₂PO₄·H₂O) or potassium buffer (K₂HPO₄-KH₂PO₄) used in the extraction of C-phycoerythrin (C-PE) from a thermotolerant strain of Potamosiphon sp. An experimental design (Minimum Run Resolution V Factorial Design) and a Central Composite Design (CCD) were used. According to the statistical results of the first design, the K-PO₄ buffer, pH, molarity, and w/v fraction are vital factors that enhance the extractability of C-PE. The construction of a CCD design of the experiments suggests that the potassium phosphate buffer at pH 5.8, longer extraction times (50 min), and minimal extraction speed (1000 rpm) are ideal for maximizing C-PE concentration, while purity is unaffected by the design conditions. This optimization improves extraction yields and maintains the desired bright purple color of the phycobiliprotein. Full article

In the present work, the low-temperature synthesis of substituted calcium hydroxyapatite (Ca₁₀(PO₄)₆(OH)₂, HAP) with copper and zinc ions on titanium substrates was performed. Initially, CaCO₃ coatings were synthesised on titanium substrate using the sol-gel method at 550 °C in a CO₂ atmosphere. Crystalline calcium hydroxyapatite was then synthesised from these CaCO₃ coatings through the dissolution-precipitation method at low temperature (80 °C). X-ray diffraction (XRD) analysis, FTIR and Raman spectroscopies, and scanning electron microscopy (SEM) were employed to evaluate the phase composition, surface functional groups, crystallinity, and morphology of the coatings. The results showed the formation of hexagonal HAP particles with a size of 20 nm at low temperature, exhibiting high homogeneity in particle size distribution. In the calcium hydroxyapatite, some of the Ca²⁺ ions were replaced by Cu²⁺ ions. Heating the mixture of Ca(NO₃)₂ and Cu(NO₃)₂ solutions at 550 °C in a CO₂ atmosphere led to the formation of copper hydroxide carbonate (malachite, Cu₂(OH)₂CO₃) along with CaCO₃. The reaction between the sol-gel precursor obtained and Na₂HPO₄ resulted in the formation of copper-substituted hydroxyapatite (Cu-HAP). Different synthesis methods were tested with Zn²⁺ ions, and on the surface of the coating, Zn(OH)(NO₃)(H₂O), Zn₃(OH)₄(NO₃)₂, and unreacted CaCO₃ were formed. Antibacterial properties of the coatings were tested using the inhibition zone method. No inhibition zones were observed for HAP. However, in the Cu and Zn containing coatings, inhibition zones were observed in the presence of a colony of B. subtilis bacteria. However, no inhibition zones were detected in the presence of E. coli bacteria. Full article

The outdoor thermal environment can be regarded as a significant factor influencing indoor thermal conditions. The application of phase change materials (PCMs) to the building envelope has the potential to improve the heat storage performance of building walls and, therefore, effectively regulate the temperature variations of the inner surfaces of walls. COMSOL Multiphysics software was adopted firstly to perform the simulations on the thermoregulation performance of phase change wall; the time duration of the temperature at the internal side maintained within the thermal comfort range was used as a quantitative evaluation index of the thermoregulation effects. It was revealed from the simulation results that the time durations of thermal comfort were extended to 5021 s and 4102 s, respectively, when the brick walls were filled with two types of composite PCMs, namely eutectic hydrate (EHS, Na₂CO₃·10H₂O and Na₂HPO₄·12H₂O with the ratio of 4∶6)/5 wt.% BN and EHS/5 wt.% BN/7.5 wt.% expanded graphite (EG), under the conditions of 18 °C ambient temperature and 60 °C heating temperature at the charging stage. Both of them were longer than 3011 s, which corresponds to a pure brick wall. EHS/5 wt.% BN/7.5 wt.% EG exhibited better leakage prevention performance and, therefore, was a candidate for actual application, in comparison with EHS/5 wt.% BN. Then, a machine learning training process focused on the temperature control effects of phase change wall was carried out using a BP neural network, where the heating surface and ambient temperature were used as input variables and the time duration of indoor thermal comfort was the output variable. Finally, the learning deviation between the raw data and the results obtained from machine learning was within 5%, indicating that machine learning can accurately predict the temperature control effects of the phase change wall. The results of the simulations and machine learning can provide information and guidance for the advantages and potentials of PCMs of hydrate salts when being applied to the building envelope. In addition, the accurate prediction of machine learning demonstrated its application prospects to the research of phase change walls. Full article

The rate of resorption of calcium phosphate self-hardening materials for bone regeneration can be changed by changing the phase composition. The Ca₃(PO₄)₂/CaCO₃/Ca(H₂PO₄)₂·H₂O/Na₂HPO₄·12H₂O system is important for the synthesis of self-curing bioactive materials with variable resorption rates by changing the ratios of the initial components. Cement compositions in twelve figurative points of a four-component composition diagram at a fixed content in the α-Ca₃(PO₄)₂ system were studied with XRD, FTIR, SEM, calorimetric, and volumetric methods to obtain an idea of the effect of composition on solubility in vitro and resorption in vivo. It was found that the presence of the highly resorbable phase of dicalcium phosphate dihydrate in cement and the substitution of phosphate ions with the carbonate ions of hydroxyapatite increased solubility in vitro and resorption in vivo. The obtained results confirm the possibility of changing the solubility of a final product in the Ca₃(PO₄)₂/CaCO₃/Ca(H₂PO₄)₂·H₂O/Na₂HPO₄·12H₂O system by changing the ratio of the initial components. Full article

The influence of ionic substitution in the Ca_1−xCo_xHPO₄·nH₂O compound was studied systematically for the first time. Among the fascinating features of these biomaterials is that they can be easily tailored for specific applications, for example, as biocements and bioceramics. Different molar concentrations of Co(NO₃)₂·6H₂O, Ca(NO₃)₂·4H₂O, and NaH₂PO₄·2H₂O compounds were employed in determining the starting solutions utilized in the present study. The experimental findings reveal that, when the Co/Ca molar ratio is below 0.67 (BCo4), Co doping (the partial substitution of Ca by Co) takes place in brushite as a monophase. However, in the Co/Ca 0.67–1.5 molar ratio range (BCo4–BCo6), biphasic Co₃(PO₄)₂·8H₂O/CaHPO₄·2H₂O crystals start to precipitate. Full Ca replacement by Co results in the precipitation of nanostructured monoclinic cobalt phosphate and orthorhombic ammonium cobalt phosphate hydrate. Subsequent X-ray photoelectron spectroscopy (XPS), powdered X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), and scanning electron microscopy (SEM) analyses, along with thermogravimetric analysis (TGA), confirmed that the starting solution ratio of Co/Ca had a significant influence on the material’s microstructure, while tuning this ratio ultimately tailored the desired properties of the material for the intended applications. Full article

Magnesium phosphate (MgP) has garnered growing interest in hard tissue replacement processes due to having similar biological characteristics to calcium phosphate (CaP). In this study, an MgP coating with the newberyite (MgHPO₄·3H₂O) was prepared on the surface of pure titanium (Ti) using the phosphate chemical conversion (PCC) method. The influence of reaction temperature on the phase composition, microstructure, and properties of coatings was systematically researched with the use of an X-ray diffractometer (XRD), a scanning electron microscope (SEM), a laser scanning confocal microscope (LSCM), a contact angle goniometer, and a tensile testing machine. The formation mechanism of MgP coating on Ti was also explored. In addition, the corrosion resistance of the coatings on Ti was researched by assessing the electrochemical behavior in 0.9% NaCl solution using an electrochemical workstation. The results showed that temperature did not obviously affect the phase composition of the MgP coatings, but affected the growth and nucleation of newberyite crystals. In addition, an increase in reaction temperature had a great impact on properties including surface roughness, thickness, bonding strength, and corrosion resistance. Higher reaction temperatures resulted in more continuous MgP, larger grain size, higher density, and better corrosion resistance. Full article

Ceramic materials in Na₂O-CaO-P₂O₅ system were obtained by firing cement-salt stone made from pastes based on powder mixtures including calcium citrate tetrahydrate Ca₃(C₆H₅O₇)₂∙4H₂O, monocalcium phosphate monohydrate (MCPM) Ca(H₂PO₄)₂∙H₂O and/or sodium dihydrogen phosphate NaH₂PO₄. The phase composition of the obtained samples of cement-salt stone after adding water, hardening and drying included brushite CaHPO₄∙2H₂O, monetite CaHPO₄ and also unreacted Ca₃(C₆H₅O₇)₂∙4H₂O, Ca(H₂PO₄)₂∙H₂O and/or NaH₂PO₄. The phase composition of ceramics in Na₂O-CaO-P₂O₅ system obtained by firing cement-salt stone was formed due to thermal conversion of hydrated salt and heterophase reactions between components presented in samples during firing. The phase composition of ceramic samples based on powder mixture of Ca₃(C₆H₅O₇)₂∙4H₂O and Ca(H₂PO₄)₂∙H₂O after firing at 900 °C included β-calcium pyrophosphate (CPP) β-Ca₂P₂O₇. The phase composition of ceramic samples based on powder mixture of Ca₃(C₆H₅O₇)₂∙4H₂O, and NaH₂PO₄ after firing at 900 °C included β-sodium rhenanite β-CaNaPO_4. The phase composition of ceramic samples based on powder mixture of Ca₃(C₆H₅O₇)₂∙4H₂O, Ca(H₂PO₄)₂∙H₂O and NaH₂PO₄ after firing at 900 °C included β-Ca₂P₂O₇, β-CaNaPO_4, double calcium-sodium pyrophosphate Na₂CaP₂O₇, and Na-substituted tricalcium phosphate Сa₁₀Na(PO₄)₇. Obtained ceramic materials in Na₂O-CaO-P₂O₅ system including biocompatible and biodegradable phases could be important for treatments of bone tissue defects by means of approaches of regenerative medicine. Full article