Formation Of Vaterite Research Articles

Stabilization of metastable calcium carbonate polymorphs on the surface of recycled cement paste particles: A two-step carbonation approach without chemical additives

In this study, a two-step carbonation method is developed to control the formation of calcium carbonate (Cc) polymorphs on the surface of recycled hardened cement paste (RHCP) without the use of chemical additives. In the first step, RHCP undergoes semi-dry carbonation under controlled humidity conditions, followed by wet carbonation at various temperatures in the second step. The results show that vaterite and aragonite are stabilized during the wet carbonation process, forming primarily on the surface of RHCP particles. The stabilization of the metastable Cc phases is driven by the synergistic effect of existing Cc seeds in the RHCP and the reaction temperature. A temperature range of 9–48 °C promotes the formation of vaterite, while higher temperatures (60–90 °C) lead to its dissolution. The calcite seeds present in RHCP do not enhance the formation of vaterite and aragonite during wet carbonation. This method offers a potential practical approach for valorizing concrete waste while capturing CO₂ from the atmosphere.

Synthesis of eco-friendly CaCO3@Zn-Al MMO core-shell nanoflowers photocatalyst using bio–eggshell waste for improved photocatalytic degradation of RhB under visible light irradiation

In this study, a type-I heterojunction was synthesized based on eggshell waste doped mixed metal oxide (ES@ZnAl MMO) for the degradation of RhB dye under visible light irradiation. The ES@ZnAl MMO core-shell was synthesized using waste eggshell and layered double hydroxide (LDH) as primary precursors. After their mechanochemical assembly and thermal treatment, CaCO3 was formed in both calcite and vaterite forms, alongside mixed metal oxides derived from the LDH (ZnO and Al2O3). The formation of a heterojunction between the semiconductors results in an improved activation of sites, a decrease in bandgap energy from 5.72 to 3.44 eV, and an increase in degradation capacity. The elemental composition, morphology, structural, and optical properties of the ES@ZnAl MMO nanocomposite were analyzed using various techniques. The optimal ES@ZnAl MMO photocatalyst demonstrated superior performance, reaching over 98% of RhB dye degradation under optimal conditions, outperforming pure ZnAl LDH, ZnAl MMO, and ES. After five run cycles, the ES@ZnAl MMO heterojunction still maintained a high photocatalytic performance for RhB dye (99%). Furthermore, it displayed high performance in degrading various other pollutants, including OG, IC, MB, and 2.4-DP, with degradation efficiencies of 97%, 99%, 99%, and 87%, respectively. This economically advantageous heterojunction showed its importance in environmental remediation, presenting a promising solution for addressing diverse pollution challenges.

Enhancing mechanical properties of carbonated steel slag through surfactant-assisted CaCO3 crystallization

This study investigates the enhancement of mechanical properties in carbonated steel slag through surfactant-assisted CaCO3 crystallization. Sodium dodecyl benzene sulfonate (SDBS) was employed at various concentrations (0.1–0.4 mol/L) and temperatures (20–60 °C) to modulate the carbonation process. Optimal performance was achieved with 0.2 mol/L SDBS at 40 °C, resulting in a maximum CO2 uptake of 8.51 % and a compressive strength of 62.89 MPa, 81.66 % higher than unmodified steel slag. Characterization techniques confirmed the formation of crystalline calcite, vaterite, and aragonite, contributing to improved microstructure and strength. SDBS micelles act as templates for CaCO3 nucleation and growth, with low concentrations facilitating carbonation and high concentrations inhibiting it. This research offers new insights into surfactant-assisted crystallization for enhancing carbonated steel slag properties, paving the way for high-performance, eco-friendly building materials from industrial waste.

Enhanced carbon sequestration via phosphogypsum utilization in conjunction with concrete wastewater treatment

The simultaneous utilization of concrete wastewater (CW) and phosphogypsum (PG) to mineralize CO2 for carbon reduction is a green and low-carbon treatment method. In this work, the combined carbonation process of CW and PG and the role of ammonia as an additive were investigated. The addition of ammonia balances the excess anions, inhibits CaCO3 resolvation, and enhances the gas–liquid mass transfer. The higher pH and ionic strength of CW help to accelerate the PG dissolution and increase the PG conversion rate. Simultaneously, a decalcification efficiency of 100 % for CW and a PG conversion rate of 98.00 % were achieved. This process resulted in a CO2 capture of 215.76 g CO2/kg PG, with the pH of the synergistically treated wastewater ranging from 6.43 to 7.54. Additionally, the common ionic effect of Ca2+ and SO42−, the salting effect of CW, and the salting-out effect of CO2 influenced the reaction. The formation of vaterite under pressurized conditions was primarily governed by pH, which played a key role in determining the crystal morphology. The interaction between CW and PG was further confirmed in 5 L scale-up experiments, during which ammonia recycling was also achieved. This study fully utilized CW, combining it with PG to efficiently repurpose wastewater and solid waste for resource recovery.

Innovative and environmentally friendly MICP surface curing: Enhancing mechanical and durability properties of concrete

Concrete curing is a critical factor influencing its mechanical properties and durability. Traditional curing methods, such as water curing and plastic film curing, have significant limitations, including high water consumption and environmental pollution. This study introduces Microbial Induced Carbonate Precipitation (MICP) as an innovative, environmentally friendly curing method for ready-mixed concrete, addressing the urgent need for sustainable construction practices. The feasibility of MICP surface curing is investigated through comprehensive mechanical and durability tests, coupled with microscopic analyses to understand the underlying mechanisms. The results demonstrate that MICP curing substantially enhances concrete performance. Compared to traditional water curing, the samples cured using MICP have increased compressive strength and splitting tensile strength by up to 31.69% and 24.66%, respectively. Additionally, MICP surface curing significantly reduced capillary water absorption, electric flux, and chloride ion migration coefficient by 12.83%, 15.50%, and 17.36%, respectively. It is found that the optimal concentration of Ca2+ in the MICP solution initially improves concrete performance, which then diminishes at higher concentrations due to bacterial activity inhibition. Spraying the MICP solution at appropriate intervals and increasing the number of treatments further improved concrete properties by ensuring a more extensive and dense deposition of CaCO3. Microscopic analyses, including XRD, TG, and SEM-EDS, revealed that MICP surface curing leads to the formation of vaterite and calcite, which densely cover and fill microscopic cracks and pores, ensuring adequate hydration and simultaneously enhancing the concrete's mechanical and durability properties. This study concludes that MICP surface curing provides superior performance than traditional methods and offers a more sustainable and environmentally friendly curing method.

Effectiveness and mechanism of microbial dust suppressant on coal dust with different metamorphosis degree.

The extraction of coal from open-pit mines significantly contributes to environmental degradation, posing grave risks to human health and the operational stability of machinery. In this milieu, microbial dust suppressants leveraging microbially induced carbonate precipitation (MICP) demonstrate substantial potential for application. This manuscript undertakes an exploration of the dust mitigation efficiency, consolidation attributes, and the fundamental mechanisms of microbial dust suppressants across coal dust samples with varying metamorphic gradations. Empirical observations indicate that, in resistance tests against wind and rain, lignite coal underwent mass losses of 7.43g·m-2·min-1 and 98.62g·m-2·min-1, respectively. The production of consolidating agents within the lignite dust, attributable to the microbial suppressants, was measured at 0.15g per unit mass, a value of 1.25 and 1.07 times greater than that observed in bituminous coal and anthracite, respectively. Scanning electron microscopy coupled with X-ray energy-dispersive spectroscopy (SEM-EDS) and X-ray diffraction (XRD) analyses illuminated that the consolidating products within the coal dust predominantly constituted calcite and vaterite forms of calcium carbonate. The consolidation mechanism of coal dust via microbial suppressants is articulated as follows: Subsequent to the application on coal dust, the suppressants induce the formation of carbonate precipitates with inherent adhesive properties. These carbonates affix to the surfaces of coal dust particles, progressively encapsulating them. Furthermore, they play a pivotal role in bridging and filling the interstices between adjacent dust particles, thereby culminating in the genesis of a dense, cohesive mass capable of withstanding erosive forces.

Mechanism of bacteriophage-induced vaterite formation

This study shows how bacterial viruses (bacteriophages, phages) interact with calcium carbonate during precipitation from aqueous solution. Using electron microscopy, epifluorescence microscopy, X-ray diffraction, and image analysis, we demonstrate that bacteriophages can strongly influence the formation of the vaterite phase. Importantly, bacteriophages may selectively bind both amorphous calcium carbonate (ACC) and vaterite, and indirectly affect the formation of structural defects in calcite crystallites. Consequently, the surface properties of calcium carbonate phases precipitating in the presence of viruses may exhibit different characteristics. These findings may have significant implications in determining the role of bacterial viruses in modern microbially-rich carbonate sedimentary environments, as well as in biomedical technologies. Finally, the phage-vaterite system, as a biocompatible material, may serve as a basis for the development of promising drug delivery carriers.

Crack-healing and rheological properties of high content fly ash/slag/silica fume green and sustainable cement-based materials incorporating crystalline admixture and calcium alginate biomass hydrogel

Cracking is an important factor affecting the durability of concrete. Rheological properties are important performance indicators of the workability of fresh concrete. Ion chelator (CA) is one kind of crystalline admixture, which can enhance crack-healing of concrete by promoting the formation of calcium carbonate in wet environment. Calcium alginate hydrogel (CaAlg) can maintain the humidity of cementitious matrix and promote the crystallization of inorganic minerals. Therefore, in this study, CaAlg bead was prepared to further improve the crack-healing of cementitious materials containing CA. Self-healing performance was evaluated by visual crack closure and water permeability test. Rheological property was measured by rotor rheometer. Healing mechanism of cementitious materials with CA and CaAlg was analyzed. Results showed that with the increase of CaAlg dosage, yield stress and plastic viscosity of paste decreased gradually. Meanwhile, fly ash and slag reduced viscosity of pastes, while silica fume increased the viscosity of pastes. CA could evidently improve the permeability and mechanical properties of mortar, especially for slag mortar. Self-healing performance test and characterization showed that CaAlg could further enhance crack-healing process of mortar with CA, especially for pure cement and slag mortar. Microscopic testing indicates that CaAlg could induce the formation of vaterite and calcite on its surface to further improve crack-healing efficiency.

The role of [formula omitted] on controlling the pure vaterite transformations

Vaterite calcium carbonate (CaCO3) possesses unique advantages compared to calcite; however, some critical issues need to be addressed, such as vaterite stability. Numerous studies have indicated that NH4+ can promote vaterite formation and prevent its transformation. However, as vaterite is an instantaneous microscopic process that is easy to transform, directly revealing the role of NH4+ in stabilizing vaterite remains challenging in experiments. This research aims to reveal the role of NH4+ in stabilizing vaterite and retarding phase transformations. Vaterite stabilization was investigated at different NH4+ concentrations and characterized by XRD and SEM. The reaction system’s pH, electrical conductivity, and surface tension changes were analyzed in the presence of NH4+. Computational and experimental studies were utilized to determine the role of NH4+ in the stabilization of vaterite. Results revealed that NH4+ can significantly increase the existence time of vaterite in the water solution. The density functional theory (DFT) indicated that the adsorption energy of NH4+ and vaterite (110), (112), and (114) is obviously higher than that of H2O molecules. The molecular dynamics (MD) simulation research shows that NH4+ can replace water molecules on the crystalline surface of vaterite and mainly interact with carbonate ions on the surface of vaterite. The mechanism analysis shows that the inhibitory effect of NH4+ on the phase transformation of vaterite is primarily caused by preventing the dissolution process. This study systematically explains the role of NH4+ in the stability of vaterite and further reveals that NH4+ can not only promote the formation of vaterite but also play a decisive role in inhibiting its phase transition.

Synthesis of Submicron CaCO3 Particles in 3D-Printed Microfluidic Chips Supporting Advection and Diffusion Mixing.

Microfluidic technology provides a solution to the challenge of continuous CaCO3 particle synthesis. In this study, we utilized a 3D-printed microfluidic chip to synthesize CaCO3 micro- and nanoparticles in vaterite form. Our primary focus was on investigating a continuous one-phase synthesis method tailored for the crystallization of these particles. By employing a combination of confocal and scanning electron microscopy, along with Raman spectroscopy, we were able to thoroughly evaluate the synthesis efficiency. This evaluation included aspects such as particle size distribution, morphology, and polymorph composition. The results unveiled the existence of two distinct synthesis regimes within the 3D-printed microfluidic chips, which featured a channel cross-section of 2 mm2. In the first regime, which was characterized by chaotic advection, particles with an average diameter of around 2 μm were produced, thereby displaying a broad size distribution. Conversely, the second regime, marked by diffusion mixing, led to the synthesis of submicron particles (approximately 800-900 nm in diameter) and even nanosized particles (70-80 nm). This research significantly contributes valuable insights to both the understanding and optimization of microfluidic synthesis processes, particularly in achieving the controlled production of submicron and nanoscale particles.

Preferential formation of uniform spherical vaterite by harnessing vortex flows and integrated CO2 capture and mineralization

The use of calcium bearing resources to facilitate solvent regeneration and CO2 reuse via carbon mineralization offers a low energy pathway for the production of calcium carbonate. However, a crucial challenge is the lack of specificity in the formation of various calcium carbonate polymorphs during carbon mineralization. One of the less explored but highly effective approaches to tune the morphology and crystal structure of specific carbonate phases involves tuning vortex flows. This approach is an alternative to utilizing chemical reagents that need to be regenerated for tuning the morphologies and crystalline structures to direct the formation of specific carbonate phases. In this study, the efficacy of using homogeneous vortex flows in limiting the agglomeration of carbonate particles and directing the formation of metastable vaterite phases is discussed and contrasted with the influence of inhomogeneous conventional feed flow patterns on precipitated calcium carbonate (PCC). Herein, a Taylor-Couette Carbonate Conversion (TC3) reactor is used to direct the formation of spherical vaterite particles with uniform particle size distribution preferentially over calcite and other phases. The formed vortex patterns inside TC3 reactor provide homogeneous reaction spaces conducive to PCC formation, ensuring uniform mixing throughout the process. By increasing the rotational speed and the residence time, higher purity carbonates with more uniform sizes are obtained. Furthermore, preferential vaterite formation is also observed in leachates obtained from alkaline industrial residues such as construction and demolition waste and steel slag. Thus, the proposed approach is effective in harnessing multiple waste streams such as CO2 emissions and alkaline industrial residues to produce calcium carbonate phases such as vaterite with structural and morphological specificity.

Production of vaterite via wet carbonation of carbide residue: Enhancing cement properties and CO2 sequestration

The influence of limestone powder (primarily composed of calcite) on hydration and properties of concrete has been extensively researched. However, there is limited understanding of how different calcium carbonate (CC) polymorphs affect cement hydration due to the difficulty in formation of vaterite. Therefore, preparing calcite and vaterite from solid waste carbide residue (CS) by wet carbonation and examining influence of these two CC polymorphs (0–20 %) on cement hydration and properties are comprehensive investigated in the paper. The results reveal that pure cubic calcite can be obtained through CS carbonation, while high-purity spherical vaterite can be synthesized using glycine as a regulator. The specific surface area (SSA) of spherical vaterite (15.47 m2/g) is approximately three times that of calcite (4.8 m2/g) with a comparable particle size distribution (PSD). The addition of calcite reduces the flowability of cement, whereas vaterite enhances it. The cement mortar with calcite demonstrates a lower compressive strength, while the incorporation of vaterite results in a higher or comparable compressive strength in contrast to control sample. Compared with control cement hydration, new hydration products, like monocarbonate aluminate and hemicarbonate aluminate, are formed with the addition of both calcite and vaterite. The metastable vaterite exhibits increased reactivity. The research presents a novel approach for the valorisation of solid wastes through CO2 sequestration, offering insights into the preparation of highly added-value products.

Renewable ammonium chloride-induced calcium leaching of gold and copper tailings and selective preparation of vaterite CaCO3 by CO2 mineralization

This study introduced a high-value green processing solution for copper tailings to prepare high-purity vaterite from gold-copper tailings. The active reaction components were determined through Gibbs free energy calculations. The study discusses the impact of different experimental parameters on the leaching rate of Ca2+ and the degree of mineralization in gold-copper tailings, and then considers the influence of different dispersants on improving the stability of vaterite. The results show that the optimal leaching efficiency of Ca2+ in the NH4Cl solution is 75%, and the optimal mineralization efficiency is 87%. Under appropriate mineralization conditions, vaterite CaCO3 with d50 < 12 μm, a purity of 98%, and a whiteness of 98.7% can be prepared. The precipitated vaterite is affected by the pH swing method connected with the neutralization reaction. The presence of excess NH3 and supersaturated CO2 are necessary for the formation of vaterite-type CaCO3. Morphological analysis results show that dispersants such as polyacrylamide and sodium tripolyphosphate can improve the dispersibility of vaterite, preventing agglomeration and enabling its stable existence in aqueous solutions. Nanoparticle aggregation and crystal growth are two possible mechanisms for the formation of vaterite. The leaching-mineralization cycle technology using NH4Cl as the leaching solution meets the requirements for CO2 removal and alkaline industrial waste residue treatment, while avoiding the significant consumption of chemical reagents in traditional mineralization. This method provides a pathway for producing vaterite using copper tailings and has a broad market prospect.

Size Control of Biomimetic Curved-Edge Vaterite with Chiral Toroid Morphology via Sonochemical Synthesis.

The metastable vaterite polymorph of calcium carbonate (CaCO3) holds significant practical importance, particularly in regenerative medicine, drug delivery, and various personal care products. Controlling the size and morphology of vaterite particles is crucial for biomedical applications. This study explored the synergistic effect of ultrasonic (US) irradiation and acidic amino acids on CaCO3 synthesis, specifically the size, dispersity, and crystallographic phase of curved-edge vaterite with chiral toroids (chiral-curved vaterite). We employed 40 kHz US irradiation and introduced L- or D-aspartic acid as an additive for the formation of spheroidal chiral-curved vaterite in an aqueous solution of CaCl2 and Na2CO3 at 20 ± 1 °C. Chiral-curved vaterites precipitated through mechanical stirring (without US irradiation) exhibited a particle size of approximately 15 μm, whereas those formed under US irradiation were approximately 6 μm in size and retained their chiral topoid morphology. When a fluorescent dye was used for the analysis of loading efficiency, the size-reduced vaterites with chiral morphology, produced through US irradiation, exhibited a larger loading efficiency than the vaterites produced without US irradiation. These results hold significant value for the preparation of biomimetic chiral-curved CaCO3, specifically size-reduced vaterites, as versatile biomaterials for material filling, drug delivery, and bone regeneration.

Effect of sodium chloride on yield, purity, morphology and polymorphs of calcium or magnesium carbonate sequentially precipitated from brine solution

Oilfield brine disposal in marine environments is undesirable due to concentrated salts of calcium, magnesium, sodium, and others which endanger aquatic organisms. Thus, it is paramount to precipitate the dissolved ions into stable carbonates for industrial applications. However, the effect of NaCl in the brine solution on the quantity and quality of precipitated carbonates is not yet reported. In this study, microwave plasma atomic emission spectrometer (MIP AES), x-ray diffraction (XRD), and scanning electron microscopy (SEM) were employed to investigate the effect of 0–2 M NaCl on the yield, purity, polymorph, and morphology of calcium and magnesium carbonates. The yields of 96.2% to 98.9% and 53.7% to 69.6% and the purity of 90.9% to 92.7% and 96% to 99.5% CaCO3 and MgCO3·3H2O were obtained, respectively. Moreover, the maximum yield and purity of carbonates were obtained from a brine solution of 1 M NaCl. The concentration of 0–0.5 M NaCl favored more the formation of aragonite whiskers and rhombohedral calcite whereas the concentration of 1–2 M NaCl favored more the formation of aragonite whiskers, lamella vaterite,and rhombohedral calcite. Nevertheless, only nesquehonite (MgCO3·3H2O) precipitated regardless of brine concentration. The crystal surface and length of the precipitated nesquehonite from 1 to 2 M NaCl brine were affected.

The regulation of organic molecules to the morphology and corrosion protection ability of CaCO3 coating on biomedical MgZnCa alloy

A controllable corrosion rate is an ideal condition for magnesium (Mg) alloy as biodegradable metallic materials. Calcium carbonate (CaCO3) coating has been proven to possess a robust anti-corrosion property for Mg alloy. To further regulate the morphology and corrosion protection ability of the CaCO3 coating, in current study, different organic molecules, including amino acids (Tyr and Glu), amine (DOPA), proteins (COL and BSA) and peptide (CPP), were added into the coating formation electrolyte, affecting the morphology, polymorph composition, and the crystal size distribution of precipitated CaCO3. The results revealed that Tyr exhibited little effect on the polymorph composition of the CaCO3-based coating, while Glu, DOPA, COL and BSA generally promoted the formation of vaterite but inhibited the formation of rod-like aragonite precipitates and calcite in the coatings. In contrast, CPP suppressed the precipitation of CaCO3 crystals because of its high affinity to Ca2+ ions. The addition of those organics reduced the size of calcite crystals. Consequently, the organic molecules mediated CaCO3-based coatings showed better compactness and homogeneity, which maintained the strong adhesion strength of the coatings to the substrate and further enhanced the corrosion protection abilities of the coating for the substrate. The results of the study pave the way for the development of CaCO3-based coatings with advanced properties for Mg alloys as biomedical materials.

Microbial Biomineralization of Alkaline Earth Metal Carbonates on 3D-Printed Surfaces.

The biomineralizing bacterium Sporosarcina pasteurii has attracted considerable interest in the area of geotechnical engineering due to its ability to induce extracellular mineralization. The presented study investigated S. pasteurii's potential to induce the mineralization of alkali-earth metal carbonate coatings on different polymeric 3D-printed flat surfaces fabricated by different additive manufacturing methods. The use of calcium, barium, strontium, or magnesium ions as the source resulted in the formation of vaterite (CaCO3), witherite (BaCO3), strontianite (SrCO3), and nesquehonite MgCO3·3H2O, respectively. These mineral coatings generally exhibit a compact, yet variable, thickness and are composed of agglomerated microparticles similar to those formed in solution. However, the mechanism behind this clustering remains unclear. The thermal properties of these biologically induced mineral coatings differ from their inorganic counterpart, highlighting the unique characteristics imparted by the biomineralization process. This work seeks to capitalize on the bacterium S. pasteurii's ability to form an alkali-earth metal carbonate coating to expand beyond its traditional use in geoengineering applications. It lays the ground for a novel integration of biologically induced mineralization of single or multilayered and multifunctional coating materials, for example, aerospace applications.

Quantitative phase analysis and molecular structure of human gallstones using synchrotron radiation X-ray diffraction and FTIR spectroscopy

Human gallstones are the most common disorder in the biliary system, affecting up to 20 % of the adult population. The formation of gallstones is primarily due to the supersaturating of cholesterol in bile. In order to comprehend gallstone disease in detail, it is necessary to have accurate information about phase identification and molecular structure. Different types of gallstone samples were collected from the Middle East area after surgical operations including; cholesterol, pigment, and mixed gallstones. To estimate the basic information about the stone formation and the pathophysiology of cholelithiasis as well as to classify the collected human gallstones, attenuated total reflection Fourier transform Infrared spectrometry (ATR-FTIR) was used to analyze the different gallstone structures in the wavenumber range from 400 to 4000 cm−1. Calcium bilirubinate was specified by the bands at 1662 cm−1, 1626 cm−1, and 1572 cm−1, while cholesterol rings were designated by the bands at 1464, 1438, 1055, and 1022 cm−1. It can be assumed that all samples consist of mixed gallstones based on the doublets at 1375 cm−1 and 1365 cm−1. The levels of calcium bilirubin and various minerals varied among the analyzed samples, indicating the heterogeneity in their composition and suggesting potential implications for gallstone formation. Based on the quantitative phase analysis using synchrotron radiation X-ray diffraction (SR-XRD), two phases of anhydrous cholesterol as a major content and one phase of monohydrate cholesterols as trace content represent the main components of most of the gallstones. Additional phases of calcium carbonate in the form of calcite, vaterite, aragonite, and bilirubinate were also quantified. According to the outcomes of the FTIR and the SR-XRD measurements, there exists a statistical correlation between the different types of chemical constituents of the gallstones.

Microfluidic Vaterite Synthesis: Approaching the Nanoscale Particles

The challenge of continuous CaCO3 particle synthesis is addressed using microfluidic technology. A custom microfluidic chip was used to synthesize CaCO3 nanoparticles in vaterite form. Our focus revolved around exploring one-phase and two-phase synthesis methods tailored for the crystallization of these nanoparticles. The combination of scanning electron microscopy, X-ray diffraction, dynamic light scattering, and small-angle scattering allowed for an evaluation of the synthesis efficiency, including the particle size distribution, morphology, and polymorph composition. The results demonstrated the superior performance of the two-phase system when precipitation occurred inside emulsion microreactors, providing improved size control compared with the one-phase approach. We also discussed insights into particle size changes during the transition from one-phase to two-phase synthesis. The ability to obtain CaCO3 nanoparticles in the desired polymorph form (∼50 nm in size, 86–99% vaterite phase) with the possibility of scaling up the synthesis will open up opportunities for various industrial applications of the developed two-phase microfluidic method.

Effects of NH+4 concentration on the vaterite formation via direct carbonation use waste carbide slag under the different ammonium systems

The effect of NH+4 concentration on the formation process of vaterite under three special systems containing NH+4 was investigated via direct carbonation of waste carbide slag. The synergistic effects of NH+4 with organic (CH3COO-) and inorganic (S2O2–8) systems on vaterite formation were systematically studied. The obtained particles were characterized by X-ray powder diffraction (XRD), scanning electron spectroscopy (SEM), dynamic light scattering (DLS) and thermogravimetric analysis (TGA) analytical techniques. The results show that the content of vaterite significantly increases when the presence of NH+4, and the maximum content of vaterite is 93.37%, 95.78% and 95.39% in NH4Cl, CH3COONH4 and (NH4)2S2O8 systems. The different systems affect the vaterite particle content, morphology, particle size and distribution at the same NH+4 concentration was studied. Mechanistic analysis shows that NH+4 can change the leaching rate of Ca2+, CH3COO- can adsorb on the vaterite surface, and S2O2–8 can make the CaSO4 intermediate appear in the reaction system. Apparent synergistic interactions between NH+4 and CH3COO-, S2O2–8 affect the nucleation and growth process of vaterite. This study can provide theoretical support for the preparation of vaterite, the functional utilization of waste carbide slag, and the mineralization of CO2.