Precipitated Calcium Research Articles

Pharmaceutical Equivalence of Film-Coated and Chewable Tablets: A Comparative Dissolution Study Using Pulverized Chewable Tablets

Famotidine is a histamine H2 receptor antagonist used in the treatment of gastrointestinal disorders. It is available in multiple formulations, including film-coated tablets, chewable tablets, oral suspension, and injections. The purpose of this study was to develop and evaluate the film-coated tablet (FT) containing famotidine, magnesium hydroxide, and precipitated calcium carbonate, designed to be pharmaceutically equivalent to the marketed chewable tablet (CT). To achieve the pharmaceutical equivalence of two tablets, the dissolution profiles of FT should be similar to those of CT. However, since CT is intended to be chewed before swallowing, testing it in its intact form would not provide accurate results. Therefore, pulverized chewable tablets (PCT) were used as the reference product. The dissolution, performed by the paddle method at 50 rpm, was analyzed by the validated UV method. Similarity factor (f2) and difference factor (f1) were calculated to assess the equivalence of the dissolution profiles. The results demonstrated that the dissolution profiles of the FT and CT were similar. Additionally, the acid-neutralizing capacity test confirmed the equivalence of the two antacids. This study is one of the first to propose that dissolution tests for pharmaceutical equivalence should be conducted on pulverized CTs when developing generic equivalents to CTs.

Collective molecular-scale carbonation path in aqueous solutions with sufficient structural sampling: From CO2 to CaCO3.

The carbonation reaction is essential in the global carbon cycle and in the carbon dioxide (CO2) capture. In oceans (pH 8.1) or in synthetic materials such as cement or geopolymers (pH over 12), the basic pH conditions affect the reaction rate of carbonation. However, the precipitation of calcium or magnesium carbonates acidifies the environment and, therefore, limits further CO2 capture. Here, we investigate how pH influences carbonation pathways in neutral and basic solutions at the atomic scale using reactive molecular simulations coupled with enhanced sampling methods from CO2 to calcium carbonate (CaCO3). Two distinct CO2 conversion pathways are identified: (1) CO2 hydration: CO2+H2O⇌H2CO3⇌HCO3-+H+⇌CO32-+2H+ and (2) CO2 hydroxylation: CO2+OH-⇌HCO3-⇌CO32-+H+. The CO2 hydration pathway occurs in both neutral and basic aqueous solutions, but reactions differ significantly between the two pH conditions. The formation of the CO32- is characterized by a markedly high free energy barrier in the neutral solution. The CO2 hydroxylation pathway is only found in basic solutions. Notably, the CO2 molecule exhibits a pronounced energetic preference for reacting with hydroxide ions (OH-) rather than with water molecules, resulting in significantly reduced free energy barriers along the CO2 hydroxylation pathway. The reaction rate estimation suggests that the CO2 hydroxylation path is the most favorable carbonation pathway in the basic solution. Once the CO32- anion is formed in the presence of alkali-earth (e.g., Ca2+ and Mg2+) cations, carbonate formation can proceed.

Hardness properties of calcium and magnesium ions in drinking water

The drinking water parameter - water hardness - is defined as the sum of calcium and magnesium ion concentrations. In this study, their precipitation during boiling was investigated, using water of different hardnesses, calcium to magnesium ratios, natural tap and bottled waters. During boiling, pH value, conductivity, and calcium and magnesium concentrations were measured. Further, the morphology and composition of precipitates were analyzed. Boiling tests with durations of 30 min showed only a decrease of calcium concentration by precipitation. Longer boiling of water with a high proportion of magnesium showed decreasing magnesium concentrations once the calcium precipitation was completed. Calcium carbonate precipitated as calcite and aragonite crystals with aragonite needles occurring in the presence of high magnesium concentrations. Magnesium hydroxide formed during precipitation was identified as hydromagnesite crystals with different crystallization morphologies. Unexpectedly, for a water with low and equimolar concentrations of calcium and magnesium only magnesium precipitated at the relatively low pH 8.7. In summary, calcium ions in drinking water are evaluated as being of considerably higher relevance for the hardness properties than the magnesium ions. However, the precipitation of both minerals depends on their concentrations and ratio as well as on the pH value and the water matrix.

Isolation and Characterization of Ureolytic Calcifying Bacteria from Methane Hydrate-Bearing Marine Sediments for Bio-cementation Application

In bio-calcification, microbes precipitate calcium carbonate (CaCO3), forming versatile solid substances that promotes eco-friendly materials and reduce carbon emissions. Marine bacteria can generate bio-cements to strengthen dikes and combat coastal erosion. However, the role of marine bacteria in generating bio-cements for enhancing coastal structures and combating erosion is not fully understood. This study investigates the potential of CaCO₃ precipitating bacteria isolated from methane hydrate-bearing marine sediments. Five calcifying marine bacteria were isolated using Christensen's urea agar from marine sediments collected from Gawadar coastal, Pakistan. Bacterial strains induced CaCO3 precipitation producing urease enzymes. Strains were identified as Pseudomonas putida, Bacillus altitudinis, Vibrio sp., Bacillus sp., and Vibrio plantisponsor. Energy-dispersive X-ray spectroscopy, scanning electron microscopy, and X-ray diffraction were applied for the identification and differentiation of calcite and vaterite precipitates. The growth of isolates and precipitation potential were observed optimum at 5% NaCl and pH 9.5-11. Bacillus altitudinis (ST4SD3) and Bacillus sp. (ST4SD1) produced more soluble Ca2+ (8532.53 mg/l and 7581.98 mg/l) as compare to other isolates at higher pH 10 and pH 11, favorable for CaCO3 precipitation. It is concluded that marine ureolytic bacteria possess significant potential for bio-cementation, which can stabilize methane hydrate-bearing sediments, improve soil properties, protect coastal regions from erosion, and crucial in the methane cycle, a greenhouse gas. We recommend further exploration of such bacteria's applications in marine construction and sediment stabilization to enhance the robustness and longevity of coastal infrastructures. Furthermore, such bacteria could also be beneficial in extracting gas from unconsolidated methane hydrates containing sediments.

Dual application of lotus stem in fabricating a bioreactor for the remediation of nitrate, plumbum, and carbamazepine in industrial wastewater

Addressing the treatment of complex industrial wastewater continues to be a substantial challenge within the realm of water treatment. A biofilm reactor was engineered, integrating lotus stem biochar, lotus stem biological filler, and the ZW5 strain for enhanced wastewater treatment. The removal efficiencies of nitrate (NO3--N), calcium (Ca2+), chemical oxygen demand (COD), phosphorus (PO43--P), plumbum (Pb2+), and carbamazepine (CBZ) were 98.46, 81.08, 91.79, 96.63, 97.75, and 99.26% when HRT was 3 h, pH was 7.0, Pb2+, CBZ, and influent salinity contents were 15.0, 3.0, and 1500 mg L-1. The reactor effectively fixed the microorganisms and provided a good microenvironment and niche, which was conducive to the adsorption of Pb2+ and CBZ by microorganisms and biominerals. Furthermore, the modified biochar in the reactor filler facilitated microbial metabolism and enabled indirect electron transfer. Microorganisms altered their dominant community structure in response to Pb2+ and CBZ exposure. Microorganisms maintained efficient activity through synergy and direct electron transfer through nanowires. The reactor serves as a model for pollutant removal from complex industrial wastewater, leveraging the multifaceted use of lotus stems and microbial-induced calcium precipitation.

Developing alkali-activated controlled low-strength material (CLSM) using urban waste glass and red mud for sustainable construction

Using industrial waste in controlled low-strength material (CLSM) offers many benefits and addresses waste management issues. However, identifying optimal CLSM design while balancing environmental impacts and engineering properties poses a notable challenge. Herein, new alkali-activated CLSM formulations based on urban waste glass and red mud (RM) are proposed for the first time with systematic investigations into the material properties and sustainability. The formulations involve the ternary blends of slag, glass powder (GP) and RM as the binders and crushed glass as aggregate. Our observations show RM has a clay-like texture with complex crystalline phases rich in Al and Fe. Increasing the proportion of RM to GP notably decreases the flowability, extends the setting time and impairs the mechanical properties. Nevertheless, red mud demonstrates a crucial role of reducing bleeding level especially for the mixtures with high proportions of glass aggregate. The standard leachate tests as per toxicity characteristic leaching procedure (TCLP) show the heavy metals leached from the CLSM are below the concentration limits and exhibit low mobility. The microstructural and thermodynamic analyses reveal the precipitation of calcium-(sodium-)aluminosilicate hydrate (C-(N-)A-S-H) as the major binding material. The reactive Fe and Al in red mud most probably contribute to the formation of hydrogarnet phases. Moreover, the suggested CLSM formations typically exhibit reduced carbon emissions and lower costs compared to the traditional CLSM produced with cement and fly ash, underlining their environmental sustainability and cost-effectiveness. This study provides a potential guideline for the flowable fill construction in the regions with bauxite producers.

Exploring fungal potential for microbial-induced calcite precipitation (MICP) in bio-cement production

IntroductionMicrobial-induced calcite precipitation (MICP) involves various microorganisms, such as bacteria, fungi, and algae. This study focuses on producing bio-cement using fungal species and selecting potential candidates isolated from alkaline soil of different regions of Punjab, namely, Majha, Malwa, and Doaba.MethodsThe selection of fungi isolates capable of bio-cement production involves several tests, including a urease assay and calcium precipitation. Isolates having high urease enzyme production and the ability to perform calcite precipitation are selected for instrumental analyses such as X-ray diffraction (XRD) and scanning electron microscopy (SEM). The isolates selected for further analysis are S1 (3) with 8.879 ± 2.94 µg/ml, S1 (18) with 8.421 ± 0.13 µg/ml, and S4 (1) with 10.057 ± 0.45 µg/ml urease activity and least free calcium ions that are 2.337 ± 0.5 µg/ml, 3.339 ± 0.5 µg/ml, and 4.074 ± 0.1 µg/ml respectively.Results and discussionCalcite precipitation is confirmed through XRD and field emission scanning electron microscopy (FESEM). XRD images showing calcite precipitation with sharp crystalline peaks for S1 (3), S1 (18), and S4 (1) are shown. The calcite precipitation is evident in the micrographs of FESEM. These combined results confirm the potential of urease-positive fungi to facilitate calcite production, which could lead to bio-cement development in future research.

Wharton's jelly of the umbilical cord serves as a natural biomaterial to promote osteogenesis.

Various factors can contribute to bone damage or loss, presenting challenges for bone regeneration. Our study explores the potential clinical applications of two processed forms of Wharton's jelly of the human umbilical cord for treating bone loss. Wharton's jelly from fresh umbilical cords underwent two distinct processes: (1) frozen Wharton's jelly (WJF), preserved with cryoprotective agents, and (2) decellularized Wharton's jelly matrix (WJD), prepared only via lyophilization without cryoprotectants. Both WJD and WJF are rich in collagen, hyaluronan, and polysaccharide proteins. Notably, WJD exhibited a porous structure lacking nuclei from human umbilical cord mesenchymal stem cells, unlike WJF. In direct contact experiments, WJD stimulated osteoblast migration, enhanced osteoblast maturation, and promoted calcium deposition for bone formation when administered to cultured rat osteoblasts. Furthermore, in transwell co-culture experiments, both WJD and WJF increased the rat osteoblast expression of RUNX2 and OPN genes, elevated alkaline phosphatase levels, and enhanced extracellular calcium precipitation, indicating their role in osteoblast maturation and new bone formation. Hyaluronic acid, one of the ingredients from WJD and WJF, was identified as a key component triggering osteogenesis. In vivo experiments involved creating circular bone defects in the calvarias of rats, where WJD and WJF were separately implanted and monitored over five months using micro-computerized tomography. Our results demonstrated that both WJD and WJF enhanced angiogenesis, collagen formation, osteoblast maturation, and bone growth within the bone defects. In summary, WJD and WJF, natural biomaterials with biocompatibility and nontoxicity, act not only as effective scaffolds but also promote osteoblast adhesion and differentiation, and accelerate osteogenesis.

Simultaneous removal of nitrate, copper, carbamazepine, and calcium from micropolluted water by fulvic acid through promotion of denitrification and microbial-induced calcium precipitation: Performance and mechanism

In this paper, a study of the denitrification strain Cupriavidus sp. W12 was conducted to remove copper (Cu2+), carbamazepine (CBZ), and calcium (Ca2+) by microbial-induced calcium precipitation (MICP) after adding fulvic acid (FA). After the addition of 20 mg/L FA, the removal efficiencies of nitrate (NO3–-N), Cu2+, CBZ, and Ca2+ reached 100.0 %, 98.7 %, 96.6 %, and 73.6 %, correspondingly and there was no accumulation of nitrite (NO2–-N). FA stimulated the growth of strain W12, improved electron transfer activity, and facilitated the conversion of gaseous nitrogen. The research revealed that FA might enhance microbial activity and result in a more dense and porous structure of the biological precipitate. Cu2+ and CBZ were removed by co-precipitation and adsorption. As the initial report of FA promoting MICP to remove complex pollutants, this paper offers a theoretical foundation for NO3–-N, Cu2+, CBZ, and Ca2+ remediation in micropolluted water.

Bioactive matrix scaffold of oxidized sacchachitin via green catalyst of siliacat tempo for enhancing bone regeneration

Bone regeneration remains a critical challenge in orthopedic medicine. Extracellular matrix proteins play important roles in bionic mineralization and osteogenesis. Sacchachitin nanofibers (SCNFs) oxidized via TEMPO have shown great potential as biomaterial scaffolds due to the introduction of carboxylic groups that mimic the natural extracellular matrix. However, TEMPO is harmful to the environment, which calls for greener and sustainable alternatives. Therefore, this study explored the green fabrication of oxidized-SCNFs through SiliaCat-TEMPO (STEMPO) as a renewable catalyst with various amount of oxidation agents to evaluate their bone regeneration ability. We developed an optimal STEMPO oxidation process, enabling efficient removal of most STEMPO particles through centrifugation with minimal residue. The oxidation efficiency of recovered STEMPO particles remained comparable to fresh ones. STEMPO-oxidized SCNFs, oxidized at increasing NaClO levels, showed an increase in carboxylate content, from 0.1360 mmol/g to 3.2415 mmol/g. Additionally, STEMPO-oxidized SCNFs exhibited excellent biocompatibility with MC3T3-E1 osteoblastic cells, facilitating calcium precipitation, cell migration, and osteogenic differentiation. Mixed composites of β-tricalcium phosphate (BCP) and STEMPO-oxidized SCNFs with higher oxidation levels further enhanced osteogenic differentiation. In vivo studies using a rat femur defect model showed that SCNFs at the highest oxidation level (ST100SC) significantly promoted bone regeneration to full recovery, achieving a bone volume to total tissue volume (BV/TV) ratio of 75.6 %, compared to 48.3 % in the control. These results demonstrated that STEMPO-oxidized SCNFs with higher oxidation levels can be used as a bioactive matrix scaffold to achieve full recovery of bone regeneration.

Calcium self-release bioremediation system combined with microbially induced calcium precipitation for the removal of ammonium nitrogen, phosphorus and heavy metals

Natural landscape water and substrate were taken to simulate the release of substrate pollutants in micropolluted water bodies, and a calcium silicate- sodium alginate (CS-SA) bioremediation system was constructed. The removal of ammonium nitrogen (NH4+-N), total nitrogen (TN) and Phosphate (PO43--P) were 99.14 %, 98.90 % and 84.44 %, respectively. The Ca2+ continuously released by CS-SA provided good microbial-induced calcium precipitation (MICP) conditions for Acinetobacter calcoaceticus strain HM12, and the removal efficiency of both Zn2+ and Cd2+ was 100 %, and the pH after remediation was consistent with that of natural water bodies. NH4+-N was removed by heterotrophic nitrification- aerobic denitrification (HN-AD) of strain HM12, and heavy metals and phosphorus were removed by co-precipitation and adsorption by MICP. High-throughput sequencing results showed that strain HM12 was effective as a bioinoculant for the remediation of the aquatic environment. The construction and operation of this bioremediation system provided a method for micropolluted water treatment and recovery of phosphorus and heavy metals.

Multiple effects of microbially induced calcium precipitation on bacteria under different molar volumes of organic pollutants

Microbially induced calcium precipitation (MICP) has been extensively discussed as a water treatment method. However, the impact of MICP on the selective adsorption of different organic contaminants in industrial wastewater and the metabolism and growth of bacteria has not been elucidated in detail. In this study, by comparing the differences in the metabolism and removal of bacteria by phenol, bisphenol A (BPA), and tetracycline (TC), it was found that bioprecipitates had significant differences in the adsorption capacity of organic pollutants with different molar volumes. Concurrently, bacteria produced more extracellular polymeric substances (EPS) under the influence of organic pollutants, and the self-protection mechanism of bacteria would reduce the amount of gaseous nitrogen. However, the points on the surface of EPS promoted the process of MICP, and MICP encapsulated bacteria to form precipitates to regulate bacteria in water and further improve the removal of carbon and nitrogen in water through biomineralization. This experiment provides new insights into the selective adsorption of bioprecipitates and its multiple effects on bacteria.

Effects of heat treatments on the stability, antioxidant activity and volatiles of milk and whey ultrafiltration permeates

Milk (MP) and whey (WP) ultrafiltration permeates were obtained from different dairy processing plants. The effects of pH (4 or 6) and heat treatments (63 °C, 30 min; or 110 °C, 6 min) on permeate stability were measured by the increase of turbidity, and precipitation of nitrogen and calcium. The antioxidant activity and the production of volatiles compounds, as affected by heat treatments, was also evaluated. WP showed a higher sensitivity to heat treatments than MP. Increasing heating temperature reduced the stability of permeates, with an intensified effect at pH 6. Calcium precipitation was the main factor responsible for the increase in turbidity. Lowering the pH to 4 prior to heating strongly limited the development of turbidity. Sterilisation improved antioxidant activity of both permeates, with a greater effect on WP. Sterilisation had no effect on the concentration of volatile aldehydes but promoted the formation of volatile sulfur compounds, and more significantly in WP.

Effects of xylan-modified precipitated calcium carbonate filler on the properties of paper

Abstract The use of mineral-based fillers tends to reduce the mechanical properties of paper, which can limit their application. The filler surface modification is a significant treatment to overcome this limitation. This research aims to offer a novel modified mineral-based filler to provide its industrial application. The surface of precipitated calcium carbonate (PCC) was modified with xylan (XS), which is a type of hemicellulose, a polysaccharide consisting mainly of xylose residues. It is used as a filler at different filler dosage levels in paper pulp. Modified PCC(MPCC) was characterized with Fourier transform infrared spectroscopy, Thermogravimetric analysis, X-ray photoelectron spectroscopy, X-ray diffraction and Field-emission scanning electron microscopy analyses. The analysis demonstrated that the MPCC filler surface was coated with XS successfully. The effect of PCC and MPCC-filled hand-sheet paper physical, chemical and optical properties were studied. The experimental results showed that the mechanical (tensile, burst, tear strength) and optical (brightness, opacity) of hand-sheet paper filled with MPCC were significantly improved compared with unmodified PCC-filled paper at the same ash content. The filler retention of PCC and MPCC fillers in paper was investigated, and the MPCC filler showed better filler retention properties in paper stock than the PCC filler.

Changes of epidermal proteins immunolocalization in the corneous layer from embryonic to definitive avian beak

The process of keratinization and cornification in the developing beak has been studied through immunofluorescence and immunogold electron microscopy in chick and zebrafinch embryos. After the curved beak anlagen appears at the tip of the maxillar bone, 5–8 layers of embryonic epidermis are generated from the basal layer of the epidermis. These cells are weakly immunoabeled for IFKs (Intermediate Filament Keratins) and more intensely for scaffoldin, a protein of the EDC (Epidermal Differentiation Complex) involved in the soft keratinization of the embryonic epidermis. Immunolabeling for CBPs (Corneous Beta Proteins) is visible in the transitional embryonic layers that are temporarily generated between the embryonic and definitive beak epidermis. The electron microscope reveals that intermediate layers contain immunolabeled periderm granules for scaffoldin mixed with bundles of corneous material immunolabeled for CBPs. Intense CBPs labeling occurs in the compacting corneous bundles of beta-keratinocytes in the definitive beak while scaffolding labeling disappears. The embryonic epidermis is sloughed before hatching. Sox (Sulfhydryl Oxidase) immunolabeling reveals that the enzyme is almost absent in embryonic layers but is present in transitional and definitive beta-keratinocytes. This indicates the formation of cross-linked disulfide bonds in the definitive corneous layer of the beak. Some calcium precipitation, suggested from von Kossa staining, occurs in the corneous layers only on the 18th day of development in the chick, in preparation for hatching.

Impact of the biogas impurities on the quality of the precipitated calcium carbonate in the regenaration stage of a chemical absorption biogas upgrading unit

Combining Carbon Capture and Storage (CCS) with producing competitive secondary raw materials is key to decarbonizing industry and reducing resource extraction. Biogas upgrading to biomethane stand out as an alternative, but a significant gap remains in integrating this process within a circular economy framework. This issue has been recently addressed by a process that integrates biogas upgrading via caustic absorption with the production of Precipitated Calcium Carbonate (PCC) and the recovery of sodium hydroxide from waste brine solution using membrane technologies. The profitability of this approach depends on the quality of the PCC, a critical factor that this work addresses. By characterizing PCC is determined whether trace compounds in biogas contaminate the PCC and potentially affect its commercial value. It also examines the CO2 absorption process and analyzes the aqueous samples from the filtration phase of the PCC slurry. Results confirm the high purity of PCC obtained from biogas treatment using Raman spectroscopy, X-Ray Diffraction (XRD), and Scanning Electron Microscopy (SEM). The analyses show that the PCC is pure calcium carbonate, mainly in the stable calcite form, with a typical tetrahedral morphology and no detectable impurities. Characterization of aqueous solutions revealed organic trace compounds from biogas, with TOC concentrations of 9.7 (± 6.4) and 16.0 (± 8) mg C/l. Silicon measurements showed similar concentrations in the absorbent solution and filtrated PCC slurry. Additionally, ammonia escapes as gas, and hydrogen sulfide in the biogas likely contributed to sulfate salt formation. Analysis of the CO₂ absorption shows a first-order reaction with OH-, where the amount of CO₂ absorbed (46.3–50.0 g) closely matches the theoretical value of 48 g. The study reveals that most of the biogas impurities dissolve into the aqueous solution, being crucial for future studies and downstream membrane treatments, and the PCC is unaffected by these impurities with a purity suitable for commercial applications.

Evaluation of The Performance of Enzyme-Induced Calcite Precipitations (EICP) Solutions Based on pH and Electrical Conductivity

Abstract EICP is an innovative, sustainable technology that utilizes specific chemicals, particularly urea and calcium chloride, in conjunction with the urease enzyme to induce the precipitation of calcium carbonate. The abovementioned technology is widely acknowledged as contemporary and environmentally responsible, aligning with established sustainability principles and green construction criteria. The quantity of precipitated calcium carbonate is contingent upon the composition of the materials employed in the precipitation process and their respective proportions. The investigation focused on determining the best percentage of calcium carbonate precipitation by conducting experiments on different concentrations of urea, calcium chloride, and the urease enzyme and examining the specific characteristics of the chemical solution that facilitate the precipitation process. The augmentation of urea and calcium chloride to a certain proportion resulted in a corresponding augmentation in the quantity of precipitated substances such as calcium carbonate. In the course of furthering the increase process, it was observed that the value of the precipitated materials remained constant and did not exhibit any further augmentation for some mixing ratios. According to the results of current study, the best ratio to precipitated calcium carbonate can be attributed to using an optimal ratio of 1 mol/L of urea and 0.5 mol/L of calcium chloride. Due to the notable efficacy of urease, the concentration increment of urease did not exhibit significant variation beyond 1 g/l. However, the alteration in the rate of reaction velocity will influence the outcome of EICP process. The experimental results and integration of several methodologies demonstrated a positive correlation between temperature elevation and reaction rate augmentation, resulting in a rapid reaction termination.

Mechanics and microstructure analysis of geopolymer utilizing ilmenite tailing and metakaolin powder as alkali-activated materials

Geopolymers derived from bulk solid waste are considered ideal substitutes for cement-based materials in developing environmentally friendly construction materials. The utilization of solid waste tailings powder as a precursor for alkali activation of geopolymer can enhance the mechanical characteristics of geopolymer. This study conducted extensive experimental studies on the compressive strength, flexural strength, SEM microstructure, thermogravimetric curve, and variable influence of alkali-activated ilmenite tailings (IT) geopolymer mortar, using the liquid-solid ratio and the number of tailings as variables. An analysis was conducted on the mortar's mechanical characteristics, microstructure, and machine-learning properties. Furthermore, the impact of different atomic ratios on the structure and characteristics of geopolymer mortars was also examined. The test results revealed that the metakaolin-iron titanium tailings geopolymer, when doped with 10% ilmenite tailings, exhibited a compressive strength of 72.30MPa at 14 days. Similarly, the flexural strength of the geopolymer reached 4.76MPa at 14 days when doped with 30% ilmenite tailings. XRD analysis showed that Magnesiohornblende particles Mg-F-A-S-H and C-A-S-H gel had positive and negative correlations, respectively, with the tailings doping level. TG results indicated that the specimens exhibit enhanced thermal stability following treatment with tailings. SEM analysis revealed that combining ilmenite tailings with metakaolin formed Me-(F)-A-S-H gels. The examination of surface porosity, pore shape, and unreacted material determined that adding ilmenite tailings increased the Si/Al and Fe/Si ratios, enhancing the transformation of the lamellar structure to the three-dimensional disordered gel mesh structure. Additionally, the tailings contributed a significant amount of Ca, elevating the Ca/Na ratio (0.1−0.6) and triggering calcium precipitation within a Ca/Si range of 0.03−0.2. This increase in calcium led to a decrease in the sample's strength as the curing time was extended. Based on prior research and the application of the Gray Wolf optimization algorithm in extreme learning, a clear negative correlation was identified between the liquid-solid ratio and strength. Furthermore, increasing the Si/Al ratio enhanced the geopolymer's strength, while an extended curing time negatively correlated with strength. The impact of tailings mixing was deemed insignificant when the tailings amount did not exceed 20%. Geopolymers may derive significant environmental and industrial benefits from the improvement of their mechanical properties, thermal stability, and optimization using machine learning.

Application of Microbial-Induced Carbonate Precipitation for Disintegration Control of Granite Residual Soil

Granite residual soil is widely distributed in Southeastern China. Such soils exhibit mechanical characteristics such as loose, rich cracks and easy disintegration, resulting in severe soil erosion disasters under rainfall conditions. Microbial-induced carbonate precipitation (MICP) is a green alternative for soil stabilization. In this study, a new strategy for the disintegration control of granite residual soil using MICP technology is proposed. The effects of the bacterial solution concentration, the cementation solution concentration, and the treatment cycle are investigated through a disintegration test. The optimal treatment parameters for granite residual soil using MICP technology are determined by analyzing the disintegration processes and residual quality indicators of disintegration. The results show that the treated samples have three types of disintegration: complete disintegration, incomplete disintegration, and non-disintegration. The precipitated calcium carbonate (CaCO3) bonds the soil particles and fills the pores. Taking into account the effectiveness and cost and a bacterial solution concentration OD600 = 0.75, five cycles of MICP treatment with a cementation solution concentration of 1.2 mol/L is optimal for the disintegration control of granite residual soil. The cementation-action effects of CaCO3 are verified through scanning electron microscopy (SEM) tests with an energy-dispersive X-ray (EDX) spectroscope. These findings suggest that MICP is a promising candidate to control the disintegration of granite residual soil.

Ammonium nitrogen and phosphorus removal by bacterial-algal symbiotic dynamic sponge bioremediation system in micropolluted water: Operational mechanism and transformation pathways

Construct a bacteria-algae symbiotic dynamic sponge bioremediation system to simultaneously remove multiple pollutants under micro-pollution conditions. The average removal efficiencies of NH4+-N, PO43−-P, total nitrogen (TN), and Ca2+ were 98.35, 78.74, 95.64, and 84.92 %, respectively. Comparative studies with Auxenochlorella sp. sponge and bacterial sponge bioremediation system confirmed that NH4+-N and TN were mainly removed by bacterial heterotrophic nitrification - aerobic denitrification (HN-AD). PO43−-P was removed by algal assimilation and the generation of Ca3(PO4)2 and Ca5(PO4)3OH, and Ca2+ was removed by algal electron transfer formation of precipitates and microbially induced calcium precipitation (MICP) by bacteria. Algae provided an aerobic environment for the bacterial HN-AD process through photosynthesis, while respiration produced CO2 and adsorbed Ca2+ to promote the formation of calcium precipitates. Immobilization of Ca2+ with microalgae via bacterial MICP helped to lift microalgal photoinhibition. The bioremediation system provides theoretical support for research on micropolluted water treatment while increasing phosphorus recovery pathways.