In Situ Monitoring the Nucleation and Growth of Nanoscale CaCO3 at the Oil-Water Interface.

Interfaces can actively control the nucleation kinetics, orientations, and polymorphs of calcium carbonate (CaCO3). Prior studies have revealed that CaCO3 formation can be affected by the interplay between chemical functional moieties on solid-liquid or air-liquid interfaces as well as CaCO3's precursors and facets. Yet little is known about the roles of a liquid-liquid interface, specifically an oil-liquid interface, in directing CaCO3 mineralization which are common in natural and engineered systems. Here, by using in situ X-ray scattering techniques to locate a meniscus formed between water and a representative oil, isooctane, we successfully monitored CaCO3 formation at the pliable isooctane-water interface and systematically investigated the pivotal roles of the interface in the formation of CaCO3 (i.e., particle size, its spatial distribution with respect to the interface, and its mineral phase). Different from bulk solution, ∼5 nm CaCO3 nanoparticles form at the isooctane-water interface. They stably exist for a long time (36 h), which can result from interface-stabilized dehydrated prenucleation clusters of CaCO3. There is a clear tendency for enhanced amounts and faster crystallization of CaCO3 at locations closer to isooctane, which is attributed to a higher pH and an easier dehydration environment created by the interface and oil. Our study provides insights into CaCO3 nucleation at an oil-water interface, which can deepen our understanding of pliable interfaces interacting with CaCO3 and benefit mineral scaling control during energy-related subsurface operation.

Intelligent Analysis of Avian Influenza Virus Biomarkers Based on Chemiluminescence Resonance Energy Transfer and DNA Logic Analysis.

A one-step logical analysis of multiple targets remains challenging. Herein, we report a one-pot and intelligent DNA logical analysis platform for the diagnosis of avian influenza virus (AIV) biomarkers based on chemiluminescence resonance energy transfer (CRET) and logic operations. On the surface of Lum/PEI/CaCO3 microparticles, the excited state of luminol underwent CRET with fluorescein isothiocyanate or rhodamine B isothiocyanate, producing three well-separated light emissions at 425, 530, and 590 nm, respectively. Taking advantage of the close distance between fluorophores aligned by the catalytic hairpin assembly reaction, the CRET efficiency was greatly enhanced (53.1%). H1N1, H7N9, and H5N1 were detected with limits of detection values as low as 15, 34, and 58 pM, respectively. Three-input logic circuits were simultaneously conducted on the surface of Lum/PEI/CaCO3 microparticles, enabling the rapid and accurate discrimination of multiple AIV biomarkers in one solution. In terms of peak positions and the normalized value of the total peak intensity, three biomarkers can be simultaneously discriminated without any other complex operations. In summary, the CRET-based multiple analytical assay was developed as an intelligent biosensor for identifying AIV biomarkers, having promising application prospects in the field of multiple analysis and precise disease diagnosis.

Preparation and Thermal Properties of Magnetic PW@CaCO3@Fe3O4 Phase-Change Microcapsules and Their Application to Textile Fabrics.

Multifunctional thermal regulation materials with good thermal properties, efficient magnetic performance, and satisfactory interface bonding on fabrics are highly desirable for protective fabrics, building winter protection materials, medical thermal regulation materials, and special-environment work clothing. Herein, a new class of magnetic phase-change PW@CaCO3@Fe3O4 microcapsules was successfully produced by controlling the content of magnetic Fe3O4 through a self-assembly method. The microstructure, chemical composition, phase-change behavior, and magnetic properties of the products were sequentially characterized and analyzed. The findings revealed that the obtained microcapsules possessed regular spherical structure with uniform size and excellent thermal properties. Furthermore, PW@CaCO3 with Fe3O4 (i.e., 8% mass fraction) showed the highest thermal regulation and magnetic properties and reached an enthalpy value of 94.25 J·g-1, which is clearly superior to the value of 77.51 J·g-1 for PW@CaCO3 microcapsules. At the same time, the encapsulation efficiency of 38.7% and saturation magnetization of 2.50 emu·g-1 were the best among the four given samples. Therefore, the good paramagnetic feature had a significant synergistic effect on the thermal properties of the PW@CaCO3 microcapsules under study. More importantly, multifunctional fabrics loaded with PW@CaCO3@Fe3O4 microcapsules still showed an enthalpy value of 25.81 J·g-1 after several washes and have the potential to be used widely in the field of temperature control. The thermal regulation fabrics in this study exhibited excellent thermal properties and fastness, which contribute to their practical applications in advancing multifunctional textiles and high-technology modern fabrics.

Mechanism and kinetics of ultrasound-enhanced CaCO3 precipitation for indium enrichment in zinc oxide dust leaching solution.

In this study, ultrasound-enhanced calcium carbonate precipitation was used to enrich indium in zinc oxide dust leachate, and the effects of precipitation endpoint pH and ultrasound power on the indium precipitation behaviour were investigated, and the optimal conditions of ultrasound-enhanced precipitation were obtained to be the precipitation endpoint pH of 4.0 and the ultrasound power of 200 W. The precipitation rate of indium under these conditions was 99.79 %. At the same time, the effects of ultrasonication and conventional stirring on the indium precipitation kinetics were compared, which proved that ultrasound can shorten the time for precipitation to reach equilibrium and reduce the amount of calcium carbonate used, and the theory of ultrasonication activation energy was put forward. The activation energy of ultrasonication was Eu-a = 2.63 KJ/mol, and that of conventional precipitation was 9.78KJ/mol, which proved that ultrasonication could reduce the activation energy of the precipitation reaction, and promote the rapid precipitation reaction. The kinetic model of ultrasound-enhanced indium precipitation is lnC0-lnCt = exp(0.11339-318.54/W).t + A. In addition, the mechanism of ultrasound-enhanced calcium carbonate precipitation of indium was revealed by XRD, SEM-EDS, XPS and TEM analyses of the precipitated residue, it was demonstrated that ultrasound can inhibit the precipitation of zinc, and the ZnCO3 phase was found in the ultrasonically precipitated residue. This study provides a new idea for indium enrichment, and the future focus will be on the scale-up of the ultrasound-enhanced precipitation device.

Promoting microalgal biofilm formation by crushed oyster shell-hydroxyapatite layer on micropatterned aluminum coating for heavy metal ions removal.

Microalgal biomass has shown inspiring potential for the heavy metal removal from wastewater, and forming microalgal biofilm is one of the sustainable methods for the microalgal biomass production. Here we report the formation of microalgal biofilm by accelerated colonization of typical algae Chlorella on thermal sprayed aluminum (Al) coatings with biologically modified surfaces. Micro-patterning surface treatment of the Al coatings promotes the attachment of Chlorella from 6.31 % to 17.51 %. Further enhanced algae attachment is achieved through liquid flame spraying a bioactive crushed oyster shell-hydroxyapatite (CaCO3-HA) composite top layer on the micropatterned coating, reaching 46.03-49.62 % of Chlorella attachment ratio after soaking in Chlorella suspension for 5 days. The rapidly formed microalgal biofilm shows an adsorption ratio of 95.43 % and 85.23 % for low concentration Zn2+ and Cu2+ in artificial seawater respectively within 3 days. Quick interaction has been realized between heavy metal ions and the negatively-charged extracellular polymeric substances (EPS) matrix existing in the biofilm. Fourier transform infrared spectroscopy (FTIR) results indicate that both carboxyl and phosphoryl groups of biofilms are crucial in the adsorption of Cu2+ and the adsorption of Zn2+ is due to the hydroxyl and phosphate groups. Meanwhile, the biofilm could act as a barrier to protect Chlorella against the attack of the heavy metal ions with relatively low concentrations in aqueous solution. The route of quick cultivating microalgal biofilm on marine structures through constructing biological layer on their surfaces would give insight into developing new techniques for removing low concentration heavy metal ions from water for environmental bioremediation.

A simple model for predicting the hydraulic conductivity of MICP-treated sand.

In this research paper, we introduce a novel and sustainable approach for forecasting the hydraulic conductivity of sand layers subjected to microbial-induced carbonate precipitation (MICP) to mitigate the diffusion of toxic pollutants. The proposed model uniquely integrates the impact of varying CaCO3 contents on the void ratio and estimates the average particle size of CaCO3 crystals through scanning electron microscopy (SEM) analysis. By incorporating these parameters into the K-C equation, a simplified predictive model is formulated for assessing the hydraulic conductivity of MICP-treated sand layers. The model's effectiveness is validated through comparison with experimental data and alternative models. The outcomes demonstrate a substantial reduction in hydraulic conductivity, with a decrease ranging between 93 and 97% in the initial assessment and a decrease between 67 and 92% in the follow-up assessment, both at 10% CaCO3 content. Notably, the hydraulic conductivity shows an initial sharp decrease followed by stabilization. These findings provide valuable insights into improving the prediction of hydraulic conductivity in MICP-treated sand layers, promoting a sustainable method for preventing pollution dispersion.

Green and sustainable strategies to control scaling in industrial plants: investigation of the efficacy of Rosmarinus officinalis L. Extract against CaCO3 scale using experimental and theoretical approaches.

In recent years, plant extracts have attracted increased interest as green alternatives to conventional anti-scaling. This is because they contain a wide range of bioactive compounds with high performance against inorganic scale. Additionally, they are biodegradable and pose minimal risks to human health and ecosystems. The present study aimed to assess the protection offered by the Rosmarinus officinalis L. leaf extract for industrial plant surfaces against the CaCO3 scale. Before assessing the anti-scaling performance of the Rosmarinus extract, phytochemical characterisation was performed by quantitative assays and HPLC-DAD analysis. Subsequently, the inhibition potential of the extract was studied using the conductivity and LCEE tests at 25°C and TH = 40°f. In addition, SEM and XRD analysis were used to assess the effect of the extract on scale morphology and crystalline phases. Finally, DFT calculations and Monte Carlo simulation were carried out to enhance knowledge of the interaction between inhibitor molecules and CaCO3(104) and (110) surfaces and optimise [extract molecule - Ca]2+ complexes. Phytochemical analysis revealed the presence of several phenolic compounds (rosmarinic acid, vanillic acid, cinnamic acid, rutin, kaempferol, trans chalcone and quercetin). Further LCEE studies demonstrated the promising anti-scaling activity of the extract at an effective concentration of 54 mg/L. SEM micrographs and XRD diffractograms revealed a significant change in the morphology and phases of precipitated CaCO3 scales upon the addition of the inhibitor. In addition, the computational approach strongly supported the experimental results. These results underlined the Rosmarinus extract's potential as a valuable green and sustainable scaling inhibitor source.

Ultrasonic Preparation of Nano-CaCO3 Templates and Hollow Mesoporous SiO2 Nanoparticles for Voriconazole Loading.

CaCO3 nanoparticles (nano-CaCO3) as nano-templates were prepared using CaCl2 and Na2CO3 solutions under controlled sonication (19.5 kHz). Using the same ultrasonic device, subsequently, hollow mesoporous silica nanoparticles (HMSNs) were obtained by the hard template of nano-CaCO3. HMSNs were selected as carriers for the antifungal drug voriconazole (VOR) loading to overcome poor water solubility. Three-dimensional CaCO3 nanosheets HMSNs were obtained under gentle sonication. Three-dimensional CaCO3 nanosheets of 24.5 nm (hydrodynamic diameter) were obtained under 17.6 W for 3 min. HMSNs were synthesized by double-template method with nano-CaCO3 as the hard template. Transmission electron microscopy measurements showed that the prepared HMSNs possess hollow structures with particle size between 110 and 120 nm. Nitrogen physisorption at -196 °C revealed that the HMSNs had high surface area (401.57 m2/g), high pore volume (0.11 cm3/g), and uniform pore size (2.22 nm) that facilitated the effective encapsulation of VOR in the HMSNs. The loading capacity of VOR (wt%) on the HMSNs was 7.96%, and the total VOR release amount of VOR-HMSNs material was 71.40% at 480 min. The kinetic model confirmed that the release mechanism of HMSNs nanoparticles followed Fickian diffusion at pH = 7.4 and 37 °C. Moreover, the cumulative VOR release at 42 °C (86.05%) was higher than that at 37 °C (71.40%). The cumulative release amount of VOR from the VOR-HMSNs material was 92.37% at pH = 5.8 at the same temperature. Both nano-CaCO3 templates and HMSNs were prepared by sonication at 19.5 kHz. The as-prepared HMSNs can effectively encapsulate VOR and released drug by Fickian diffusion.

Highly Graphitized Coal Tar Pitch-Derived Porous Carbon as High-Performance Lithium Storage Materials.

Because of its high specific capacity and superior rate performance, porous carbon is regarded as a potential anode material for lithium-ion batteries (LIBs). However, porous carbon materials with wide pore diameter distributions suffer from low structural stability and low electrical conductivity during the application process. During this study, the calcium carbonate nanoparticle template method is used to prepare coal tar pitch-derived porous carbon (CTP-X). The coal tar pitch-derived porous carbon has a well-developed macroporous-mesoporous-microporous hierarchical porous network structure, which provides abundant active sites for Li+ storage, significantly reduces polarization and charge transfer resistance, shortens the diffusion path and promotes the rapid transport of Li+. More specifically, the CTP-2 anode shows high charge capacity (496.9 mAh g-1 at 50 mA g-1), excellent rate performance (413.6 mAh g-1 even at 500 mA g-1), and high cycling stability (capacity retention rate of about 100 % after 1,000 cycles at 2 A g-1). The clean and eco-friendly large-scale utilization of coal tar pitch will facilitate the development of high-performance anodes in the field of LIBs.

Exploring the use of clay pots as sustainable storage containers to improve water quality.

BACKGROUND: Currently, tap water consumption is not highly preferred in Egypt and around the world. People prefer to consume bottled water because they believe that it is much safer and tastes better than tap water. Unfortunately, this preference can create an economic burden for many people, especially in developing countries. Clay pots can be used to provide cool, alkaline drinking water because of their porous micro-texture, which traps pollutants. This study aimed to investigate the use of clay pots to store tap water and its impact on the requirements for drinking water quality. This is done with the intent to decrease the need for bottled water as a means of offering a more sustainable and economical option. METHODS: In this study, the efficiency of clay pots as sustainable storage containers for drinking water was tested by measuring physicochemical parameters (pH, TDS, EC, turbidity, DO, ammonia, chloride, total hardness, Ca hardness, Mg hardness, chlorine, Zn, and CaCO3) and biological parameters (TPC and Legionella). RESULTS: After 7 days of storage, the quality of the water stored in clay pots met the standards set by the Egyptian law with a significant difference (p < 0.05) before and after the storage of water It was found that the dissolved oxygen increased from 6.17 ppm to 7.52 ppm after 7 days. As for total hardness, it declined from 195 to 178 ppm. There was also a significant drop in terms of TDS from 338 to 275 ppm. Furthermore, clay pots effectively filtered out both total viable bacteria and Legionella. CONCLUSION: This study proved the efficiency of using these containers with respect to some indicator values for tap water and tank water analysis. Clay pots are an excellent, cost-effective, and sustainable alternative for storing water.

Scaling-Free Cathodes: Enabling Electrochemical Extraction of High-Purity Nano-CaCO3 and -Mg(OH)2 in Seawater.

For electrochemical application in seawater or brine, continuous scaling on cathodes will form insulation layers, making it nearly impossible to run an electrochemical reaction continuously. Herein, we report our discovery that a cathode consisting of conical nanobundle arrays with hydrophobic surfaces exhibits a unique scaling-free function. The hydrophobic surfaces will be covered with microbubbles created by electrolytic water splitting, which limits scale crystals from standing only on nanotips of conical nanobundles, and the bursting of large bubbles formed by the accumulation of microbubbles will cause a violent disturbance, removing scale crystals automatically from nanotips. Benefiting from the scaling-free properties of the cathode, high-purity nano-CaCO3 (98.9%) and nano-Mg(OH)2 (99.5%) were extracted from seawater. This novel scaling-free cathode is expected to eliminate the inherent limitations of electrochemical technology and open up a new route to seawater mining.

Decoupling of carbon burial from productivity in the northeast Indian Ocean.

The concentration of atmospheric carbon dioxide (CO2) is a crucial climate parameter as it has far-reaching implications on global temperature. The oceans are a significant sink for CO2. Biologically mediated carbon sequestration, in the form of both inorganic (CaCO3) and organic carbon (Corg), and its subsequent burial in marine sediments play a vital role in regulating atmospheric CO2. Understanding the distribution of carbon in marine sediments under different environments can help predict the fate of excess CO2 in the future. We studied the factors affecting the basin scale variation in carbon burial in the climatically sensitive northeast Indian Ocean, by using the data [CaCO3, Corg, Corg/Nitrogen, and isotopic ratio (δ13C, δ15N) of organic carbon] from a total of 718 surface sediments. The entire continental shelf and slope contain <10 % CaCO3. The highest CaCO3 is in the deepest parts of the central northeast Indian Ocean, away from the mouth of major river systems. Despite of the high productivity, the low Corg on the continental shelf is attributed to the well-oxygenated coarse-grained sediments. The lowest Corg is found in the well-oxygenated deeper central northeast Indian Ocean. Interestingly, the highest total carbon is in the deeper central and equatorial regions, far away from the highly productive marginal marine regions. Our study reveals that the grain size, terrigenous dilution, dissolved oxygen, and water masses strongly influence carbon accumulation in the northeast Indian Ocean, with only secondary influence of the productivity.

Influence of CaCO3 on Density and Compressive Strength of Calcium Aluminate Cement-Based Cementitious Materials in Binder Jetting.

We investigated the impact of CaCO3 addition on the density and compressive strength of calcium aluminate cement (CAC)-based cementitious materials in binder jetting additive manufacturing (BJAM). To confirm the formation of a uniform powder bed, we examined the powder flowability and powder bed density for CaCO3 contents ranging from 0 to 20 wt.%. Specifically, powders with avalanche angles between 40.1-45.6° formed a uniform powder bed density with a standard deviation within 1%. Thus, a 3D printing specimen (green body) fabricated via BJAM exhibited dimensional accuracy of less than 1% across the entire plane. Additionally, we measured the hydration characteristics of CAC and the changes in compressive strength over 30 days with the addition of CaCO3. The results indicate that the addition of CaCO3 to CAC-based cementitious materials forms multimodal powders that enhance the density of both the powder bed and the green body. Furthermore, CaCO3 promotes the formation of highly crystalline monocarbonate (C4AcH11) and stable hydrate (C3AH6), effectively inhibiting the conversion of CAC and showing compressive strengths of up to 5.2 MPa. These findings suggest a strong potential for expanding the use of BJAM across various applications, including complex casting molds, cores, catalyst supports, and functional architectural interiors.

Investigating the use of CaCO3 particles synthesized in the Ca(OH)2-CO2-H2O system for organic matter removal: adsorption efficiency and recyclability.

In this study, we experimentally investigate the production and characterization of CaCO3 particles through the carbonation process of Ca(OH)2 and evaluate their potential application in removing organic matter. The CaCO3 particles were characterized using BET, SEM-EDX, FT-IR, particle size, and XRD techniques. Adsorption of organic matter was studied using synthetic solutions and samples from two surface water sources. Experiments were conducted at room temperature with adsorbent dosages ranging from 1.3 to 21.5 g/L, initial dissolved organic carbon concentrations between 2.5 and 20 mg/L (initial loading: 0.1-14.6 mgDOC/gCaCO3), and a contact time of at least 5 minutes. We observed a removal efficiency of 70-80% for DOC and 90-95% for UV254 at a low concentration of organic matter (humic acids, 2.5 mgDOC/L). At a concentration of 5.0 mg DOC/L, we achieved (i) 70-90% DOC removal for humic acid, (ii) 50-65% DOC removal for one surface water sample with SUVA254 of 2.4 L/mg·m, and (iii) 20-35% DOC removal for another surface water sample with SUVA254 of 4.3 L/mg·m. Furthermore, we investigated the performance of the prepared particles in repeated usage for organics removal. In conclusion, our findings propose areas for future research including optimizing particle cycling within the reaction environment, exploring particle utilization in reactors such as an up-flow particle bed, and assessing potential applications in a membrane contactor. The environmentally friendly and non-toxic nature of CaCO3 particles emphasizes their significance in future research and applications.

Microfluidic paper-based chemiluminescence sensing platform based on functionalized CaCO3 for time-resolved multiplex detection of avian influenza virus biomarkers.

Multiplex detection can enhance diagnostic precision and improve diagnostic efficiency, providing important assistance for epidemiological investigation and epidemic prevention. There is a great need for multi-detection sensing platforms to accurately diagnose diseases. Herein, we reported a µPAD-based chemiluminescence (CL) assay for ultrasensitive multiplex detection of AIV biomarkers, based on three DNAzyme/Lum/PEI/CaCO3. Three time-resolved CL signals were sequentially generated with detection limits of 0.32, 0.34, and 0.29 pM for H1N1, H7N9, and H5N1, respectively, and with excellent selectivity against interfering DNA. The recovery test in human serum displayed satisfactory analysis capabilities for complex biological samples. The µPAD-based CL assay achieved multiplex detection within 70 s, with a high time resolution of 20 s. The proposed strategy has the advantages of low cost, high sensitivity, good selectivity, and wide time resolution, the µPAD-based CL assay has shown great potential in the early and accurate diagnosis of diseases.

Production of CaCO3-single-coated probiotics and evaluation of their spectroscopic properties, morphological characteristics, viability, and intestinal delivery efficiency.

The intake of probiotics offers various health benefits; however, their efficacy depends on the maintenance of viability during industrial processing and digestion. Probiotic viability can be compromised during encapsulation, freeze-drying, storage, and digestion, necessitating multiple coatings. This complicates production and raises costs. In this study, CaCO3-single-coated probiotics (CSCPs) were prepared, an approach rarely reported before. Through instrumental analyses, the encapsulation of probiotics within CaCO3 was confirmed, ensuring their high viability. This proposed technology effectively preserves the viability of probiotics during the encapsulation and freeze-drying processes, resulting in minimal cell loss. Moreover, CSCPs demonstrated exceptional viability performance under simulated gastric and intestinal conditions. Notably, 100% of these microorganisms reached the intestines, delivering over 10 billion CFUs of probiotics in a viable state. This study highlights the potential of CSCPs as a feasible solution for overcoming probiotic encapsulation challenges and optimizing therapeutic benefits.

Alginate microparticles containing silver@hydroxyapatite functionalized calcium carbonate composites.

This paper focuses on the preparation and characterization of antibacterial alginate microparticles containing silver@hydroxyapatite functionalized calcium carbonate composites for tissue engineering. Microparticles were prepared by cross-linking a silver@composite sodium alginate dispersion with CaCl2. This method showed a very good silver efficiency loading and the presence of silver chloride nanoparticles was detected. Silver free microparticles, containing hydroxyapatite functionalized calcium carbonates and neat alginate microparticles were prepared as well. All microparticles were characterized for water absorption and for in vitro bioactivity by immersion in simulated body fluid (SBF). Finally, antimicrobial and antibiofilm activities as well as cytotoxicity were evaluated. Microparticles containing silver@composites exhibited good antimicrobial and antibiofilm activities against Staphylococcus aureus, Staphylococcus epidermidis, Pseudomonas aeruginosa and Candida albicans, but exerted a certain cytotoxicity against the tested cell models (fibroblasts and osteoblasts). Microparticles containing hydroxyapatite functionalized calcium carbonates were found to be always less cytotoxic, also in comparison to neat alginate microparticles, proving that the presence of the inorganic matrices exerts a protective effect on microparticle cytotoxicity.

Characteristic study of biological CaCO3-supported nanoscale zero-valent iron: stability and migration performance.

nZVI has attracted much attention in the remediation of contaminated soil and groundwater, but the application is limited due to its aggregation, poor stability, and weak migration performance. The biological CaCO3 was used as the carrier material to support nZVI and solved the nZVI agglomeration, which had the advantages of biological carbon fixation and green environmental protection. Meanwhile, the distribution of nZVI was characterised by SEM-EDS and TEM carefully. Subsequently, the dispersion stability of bare nZVI and CaCO3@nZVI composite was studied by the settlement experiment and Zeta potential. Sand column and elution experiments were conducted to study the migration performance of different materials in porous media, and the adhesion coefficient and maximum migration distances of different materials in sand columns were explored. SEM-EDS and TEM results showed that nZVI could be uniformly distributed on the surface of biological CaCO3. Compared with bare nZVI, CaCO3@nZVI composite suspension had better stability and higher absolute value of Zeta potential. The migration performance of nZVI was poor, while CaCO3@nZVI composite could penetrate the sand column and have good migration performance. What's more, the elution rates of bare nZVI and CaCO3@nZVI composite in quartz sand columns were 5.8% and 51.6%, and the maximum migration distances were 0.193 and 0.885 m, respectively. In summary, this paper studies the stability and migration performance of bare nZVI and CaCO3@nZVI composite, providing the experimental and theoretical support for the application of CaCO3@nZVI composite, which is conducive to promoting the development of green remediation functional materials.

The effects of impurities in carbide slag on the morphological evolution of CaCO3 during carbonation.

Carbide slag (CS) is a kind of solid waste generated by the hydrolysis of calcium carbide for acetylene production. Its major component is Ca(OH)2, which shows great potential in CO2 mineralization to produce CaCO3. However, the types of impurities in CS and their mechanisms for inducing the morphological evolution of CaCO3 are still unclear. In this work, the influence of impurities in CS on the morphology evolution of CaCO3 was investigated. The following impurities were identified in the CS: Al2O3, MgO, Fe2O3, SiO2 and CaCO3. Ca(OH)2 was used to study the influence of impurities (Al2O3 and Fe2O3) on the evolution of CaCO3 morphology during CS carbonation. Calcite (CaCO3) was the carbonation product produced during CS carbonation under varying conditions. The morphology of calcite was changed from cubic to rod-shaped, with increasing solid-liquid ratios. Moreover, rod-shaped calcite was converted into irregular particles with increasing CO2 flow rate and stirring speed. Rod-shaped calcite (CaCO3) was formed by CS carbonation at a solid-liquid ratio of 10:100 under a stirring speed of 600 rpm and a CO2 flow rate of 200 ml/min; and spherical calcite was generated during Ca(OH)2 carbonation under the same conditions. Al2O3 impurities had negligible effects on spherical CaCO3 during Ca(OH)2 carbonation. In contrast, rod-shaped CaCO3 was generated by adding 0.13 wt% Fe2O3 particles, similar to the content of Fe2O3 in CS. Rod-shaped calcite was converted into particulate calcite with increasing Fe2O3 content. The surface wettability and surface negative charge of Fe2O3 appeared to be responsible for the formation of rod-shaped CaCO3. This study enhances our understanding and utilization of CS and CO2 reduction and the fabrication of high-value rod-shaped CaCO3.

Development and characterization of antacid microcapsules to buffer the acidic intervertebral disc microenvironment.

During intervertebral disc (IVD) degeneration, microenvironmental challenges such as decreasing levels of glucose, oxygen, and pH play crucial roles in cell survival and matrix turnover. Antacids, such as Mg(OH)2 and CaCO3, entrapped in microcapsules are capable of neutralizing acidic microenvironments in a controlled fashion and therefore may offer the potential to improve the acidic niche of the degenerated IVD and enhance cell-based regeneration strategies. The objectives of this work were, first, to develop and characterize antacid microcapsules and assess their neutralization capacity in an acidic microenvironment and, second, to combine antacid microcapsules with cellular microcapsules in a hybrid gel system to investigate their neutralization effect as a potential therapeutic in a disc explant model. To achieve this, we screened five different pH- neutralizing agents (Al(OH)3, Mg(OH)2, CaCO3, and HEPES) in terms of their pH neutralization capacities, with Mg(OH)2 or CaCO3 being carried forward for further investigation. Antacid-alginate microcapsules were formed at different concentrations using the electrohydrodynamic spraying process and assessed in terms of size, buffering kinetics, cell compatibility, and cytotoxicity. Finally, the combination of cellular microcapsules and antacid capsules was examined in a bovine disc explant model under physiological degenerative conditions. Overall, CaCO3 was found to be superior in terms of neutralization capacities, release kinetics, and cellular response. Specifically, CaCO3 elevated the acidic pH to neutral levels and is estimated to be maintained for several weeks based on Ca2+ release. Using a disc explant model, it was demonstrated that CaCO3 microcapsules were capable of increasing the local pH within the core of a hybrid cellular gel system. This work highlights the potential of antacid microcapsules to positively alter the challenging acidic microenvironment conditions typically observed in degenerative disc disease, which may be used in conjunction with cell therapies to augment regeneration.