Search Results (48)

The synthesis of calcium carbonate (CaCO₃) nanoparticles has gained an increasing interest due to their improved properties and diverse industrial applications. Among various synthesis techniques, the mechanochemical synthesis process has emerged as a promising route for nano-CaCO₃ synthesis. A high-energy ball mill is required for synthesizing nano-CaCO₃, whereas post-milling heat treatment facilitates completing the reaction that remains incomplete during milling. Post-milling heat treatment may also influence the properties of synthesized CaCO₃, which has not yet been thoroughly investigated. This study investigated the influence of post-milling heat treatment on the polymorphs, micromorphology, and particle size distribution of CaCO₃. The results indicated that the heat treatment of the as-milled powder enhanced the homogeneity of crystal polymorphs while maintaining the particle sizes within the nano-range (<100 nm). X-ray diffraction (XRD) analysis identified two polymorphs (vaterite and calcite) in samples obtained from different milling intensities. However, after heat treatment, all vaterite transformed into calcite. A bimodal particle size distribution was observed in CaCO₃ nanoparticles and was influenced by both the milling and heating intensities. It was observed that 60 min heat applied to 30 min as-milled powder was enough to produce nano-CaCO₃ (<50 nm) where the percentage of larger particles (<250 nm) became negligible (~1%). Micromorphology images confirmed the transformation of crystal polymorphs and the reduction in particle size. Full article

The dynamic evolution of alkalinity during hydration/carbonation of CO₂-conditioned cements results in the formation of polymorphic hydrated calcium silicates (C-S-H), whose differences in carbon sequestration capacity have not been systematically investigated. However, the micro-nano structures and carbon sequestration capacities of C-S-H are controlled by the dynamic effects of pore solution alkalinity and Ca/Si. Accordingly, different alkalinity and Ca/Si were set to simulate the cement hydration environment for the synthesis of C-S-H, and tests such as thermogravimetric and ²⁹Si nuclear magnetic resonance (NMR) were used to investigate the effects and mechanisms of initial alkalinity and Ca/Si on the morphology of the synthesized C-S-H, the CO₂ uptake. The results showed that the C-S-H synthesized at pH 7.2–12.0 and Ca/Si ratio of 1.0–2.3 was in flocculated and acicular forms, which were well crystallized and dominated by Q², while its CO₂ uptake was positively correlated with Ca/Si. On the contrary, the synthesized C-S-H was poorly crystallized under the conditions of pH increasing to 13.5 and Ca/Si ratios of 1.0–2.3. With the increase in Ca/Si, the synthesized C-S-H evolved from Q²-dominated foil to Q¹-dominated porous structure, and its CO₂ uptake was non-positively correlated with Ca/Si. This was mainly related to the average pore diameter of C-S-H and its silica-oxygen tetrahedral structure. This was mainly related to the average pore diameter of C-S-H and its silica-oxygen tetrahedral structure. Full article

Crystal violet dye poses significant environmental and human health risks due to its toxicity, persistence, and bioaccumulative nature. It contributes to potential carcinogenicity, cytotoxicity, and systemic toxicity upon human exposure. To address this issue, a novel SrCO₃/MgO/CaO/CaCO₃ nanocomposite was synthesized using the Pechini sol-gel method, producing AE500 and AE700 at 500 and 700 °C, respectively, for the efficient removal of crystal violet dye from aqueous media. X-ray diffraction (XRD) analysis confirmed the formation of crystalline phases, with average crystallite sizes of 64.53 nm for AE500 and 75.34 nm for AE700. Energy-dispersive X-ray spectroscopy (EDX) revealed elemental compositions with variations in carbon, oxygen, magnesium, calcium, and strontium percentages influenced by synthesis temperature. Field-emission scanning electron microscopy (FE-SEM) showed morphological differences, where AE500 had irregular polyhedral structures, while AE700 exhibited more compact spherical formations, with average grain sizes of 99.98 and 132.23 nm, respectively. High-resolution transmission electron microscopy (HR-TEM) confirmed the structural integrity and nano-scale morphology, showing aggregated irregularly shaped particles in AE500, while AE700 displayed well-defined polyhedral and nearly spherical nanoparticles. The calculated average particle diameters were 21.67 nm for AE500 and 41.19 nm for AE700, demonstrating an increase in particle size with temperature. Adsorption studies demonstrated maximum capacities of 230.41 mg/g for AE500 and 189.39 mg/g for AE700. The adsorption process was exothermic, spontaneous, and physical, following the pseudo-first-order kinetic model and Langmuir isotherm, indicating monolayer adsorption onto a homogenous surface. Full article

This study introduces a novel paper coating approach using modified zinc oxide (ZnO), providing a comparison with conventional materials used in the paper industry. The research focused on determining the concentration for effective microbial growth inhibition and evaluates the impact of different ZnO types on coated-paper properties, including antimicrobial activity, surface morphology, tensile strength, and water absorption. Specifically, ZnO microparticles (ZnO_ws), ZnO nanoparticles (ZnO_np), and modified ZnO_np (ZnO_np-CaCO₃, with a core–shell structure composed of calcium carbonate [CaCO₃] and nano-zinc oxide) were incorporated into coating formulations at varying concentrations (0 × MIC, 1 × MIC, 2 × MIC, and 3 × MIC, based on minimum inhibitory concentrations [MICs]). The results demonstrated that among all tested microorganisms, ZnO_np-CaCO₃ showed the lowest MIC values. ZnO_np-CaCO₃-coated paper exhibited superior antimicrobial activity against both Gram-positive and Gram-negative bacteria, as well as fungi, outperforming ZnO_ws and ZnO_np. At 1 × MIC, %inhibition for E. coli, S. aureus, and A. niger were 98.3%, 99.1%, and 90.8%, respectively. Additionally, ZnO_np-CaCO₃ coatings caused minimal color change in the paper compared to the other ZnO variants. The coating did not negatively impact the mechanical properties of the paper across all ZnO types and concentrations. Water absorption tests showed increased hydrophobicity with higher ZnO content, with ZnO_np and ZnO_np-CaCO₃ exhibiting greater reductions in water absorption than ZnO_ws. Overall, ZnO_np-CaCO₃ showed strong potential as an antimicrobial agent for paper surfaces, making it ideal for packaging and hygiene products. By partially replacing ZnO_np with inexpensive CaCO₃ core particles, ZnO_np-CaCO₃ delivers enhanced performance, reduced costs, and greater sustainability for large-scale applications. Full article

Colon cancer is the third most common cancer worldwide, with high mortality. Adverse side effects and chemoresistance of the first-line chemotherapy 5-fluorouracil (5-FU) have promoted the widespread use of combination therapies. Thymoquinone (TQ) is a natural compound with potent antioxidant activity. Loading antioxidants into nano delivery systems has been a major advance in enhancing their bioavailability to improve clinical application. Hence, this study aimed to prepare the optimal TQ-loaded calcium carbonate nanoparticles (TQ-CaCO₃ NPs) and investigate their therapeutic potential and underlying molecular mechanisms of TQ-CaCO₃ NPs in combination with 5-FU against colon cancer. Firstly, we developed purely aragonite CaCO₃ NPs with a facile mechanical ball-milling method. The pH-sensitive and biocompatible TQ-CaCO₃ NPs with sustained release properties were prepared using the optimal synthesized method (a high-speed homogenizer). The in vitro study revealed that the combination of TQ-CaCO₃ NPs (15 μM) and 5-FU (7.5 μM) inhibited CT26 cell proliferation and migration, induced cell apoptosis and cell cycle arrest in the G₀/G₁ phase, and suppressed the CT26 spheroid growth, exhibiting a synergistic effect. Finally, network pharmacology and molecular docking results indicated the potential targets and crucial signaling pathways of TQ-CaCO₃ NPs in combination with 5-FU against colon cancer. Therefore, TQ-CaCO₃ NPs combined with 5-FU could enhance the anti-colon cancer effects of 5-FU with broader therapeutic targets, warranting further application for colon cancer treatment. Full article

Nano-calcium carbonate (NC) is a novel ultrafine solid powder material that possesses quantum size effects, small size effects, surface effects, and macroscopic quantum effects that ordinary calcium carbonate lacks. As a nanomaterial with superior properties, graphene oxide (GO) has been studied extensively in the field of construction. In microscopic characterization, the reaction between NC and tricalcium aluminate (C₃A) formed a new hydration product, hydrated calcium aluminum carbonate (C₃A·CaCO₃·11H₂O), which enhanced the arrangement of hydration products and optimized the distribution of pore size in the mortar. Regarding the mechanical properties, the addition of GO and NC significantly enhanced the early-age mechanical performance of the mortar. In terms of durability, the incorporation of GO and NC significantly improved the water permeability, chloride ion permeability, and resistance to sulfate attack of the cement mortar. In this study, it was found that adding 1 wt% NC and 0.02 wt% GO not only improves the mechanical and durability properties but also promotes the hydration reaction according to the microstructure analysis. With the help of NC, compared with other studies, the amount of GO is reduced, while the cost is reduced, and the application of GO in the field of cement-based materials is promoted. Full article

The amount of by-products/waste in the fish industry is roughly 50%. Fish bones could be used to produce nanoparticles, which may have potential use in the food industry as a novel calcium source and at the same time, contribute to reduce waste production. The objective of this study was to evaluate the bioavailability of nano-size salmon fish bone particles compared to micro-size salmon fish bone particles, and calcium carbonate. The study was carried out in 21–28-day-old C57BL/6 male mice fed for 21 days with the experimental diets. The groups were as follows: CaCO₃ 0.5% Ca (CN 0.5); CaCO₃ 1.0% Ca (CN 1.0); salmon fish bone (SFB) microparticles 0.5% Ca (MP 0.5); SFB microparticles 1.0% Ca (MP 1.0); SFB nanoparticles 0.5% Ca (NP 0.5); and SFB nanoparticles 1.0% Ca (NP 1.0). Calcium bioavailability, defined as the percent calcium in femur showed an increasing trend from CN 0.5 to NP 1.0 group. According to ANCOVA, the greatest Ca content was observed in the NP 1.0 group compared with all groups but NP 0.5. In conclusion, in a murine model, salmon fish bone nanoparticles present higher calcium bioavailability than salmon fish bone microparticles, and both, in turn, have better bioavailability than calcium carbonate. Full article

Nano- and microparticles are increasingly widely used in biomedical research and applications, particularly as specific labels and targeted delivery vehicles. Silica has long been considered the best material for such vehicles, but it has some disadvantages limiting its potential, such as the proneness of silica-based carriers to spontaneous drug release. Calcium carbonate (CaCO₃) is an emerging alternative, being an easily available, cost-effective, and biocompatible material with high porosity and surface reactivity, which makes it an attractive choice for targeted drug delivery. CaCO₃ particles are used in this field in the form of either bare CaCO₃ microbeads or core/shell microparticles representing polymer-coated CaCO₃ cores. In addition, they serve as removable templates for obtaining hollow polymer microcapsules. Each of these types of particles has its specific advantages in terms of biomedical applications. CaCO₃ microbeads are primarily used due to their capacity for carrying pharmaceutics, whereas core/shell systems ensure better protection of the drug-loaded core from the environment. Hollow polymer capsules are particularly attractive because they can encapsulate large amounts of pharmaceutical agents and can be so designed as to release their contents in the target site in response to specific stimuli. This review focuses first on the chemistry of the CaCO₃ cores, core/shell microbeads, and polymer microcapsules. Then, systems using these structures for the delivery of therapeutic agents, including drugs, proteins, and DNA, are outlined. The results of the systematic analysis of available data are presented. They show that the encapsulation of various therapeutic agents in CaCO₃-based microbeads or polymer microcapsules is a promising technique of drug delivery, especially in cancer therapy, enhancing drug bioavailability and specific targeting of cancer cells while reducing side effects. To date, research in CaCO₃-based microparticles and polymer microcapsules assembled on CaCO₃ templates has mainly dealt with their properties in vitro, whereas their in vivo behavior still remains poorly studied. However, the enormous potential of these highly biocompatible carriers for in vivo applications is undoubted. This last issue is addressed in depth in the Conclusions and Outlook sections of the review. Full article

The sustainable microwave (MW) synthesis of hydroxyapatite (HAp) from decarbonized eggshells was investigated. Decarbonization of eggshells, as a natural source of calcium carbonate (CaCO₃), was carried out in the current study at ambient conditions to reduce the footprint of CO₂ emissions on our environment where either calcination or acidic direct treatments of eggshells produce CO₂ emissions, which is a major cause for global warming. Eggshell decarbonization was carried out via the chemical reaction with sodium hydroxide (NaOH) alkaline solution in order to convert eggshell waste into calcium hydroxide (Ca(OH)₂) and simultaneously store CO₂ as a sodium carbonate (Na₂CO₃) by-product which is an essential material in many industrial sectors. The produced Ca(OH)₂ was mixed with ammonium dihydrogen phosphate (NH₄H₂PO₄) reagent at pH~11 before being subjected to MW irradiation at 2.45 GHz frequency for 5 min using 800 Watts to prepare HAp. The prepared Nano-HAp was characterized using X-ray diffraction (XRD) where the crystal size was ~28 nm using the Scherrer equation. The elongated rod-like nano-HAp crystals were characterized using scanning electron microscopy (SEM) equipped with dispersive energy X-ray spectroscopy (EDS), Fourier transform infrared spectroscopy (FTIR), and transmission electron microscopy (TEM). MW synthesis of decarbonized eggshells is considered as a sustainable and environmentally friendly route to produce promising bioceramics such as nano-HAp. Concurrently, decarbonization of eggshells offers the ability to store CO₂ as a high value-added Na₂CO₃ material. Full article

Fillers have been widely used in natural rubber (NR) products. They are introduced to serve as a strategy for modifying the final properties of NR vulcanizates. Silica and calcium carbonate (CaCO₃) are among the fillers of choice when the color of the products is concerned. In this case, a special focus was to compare the vulcanizing efficiency of NR filled with two different filler types, namely nano-sized silica and micrometer-sized CaCO₃. This study focused on the effects of the loading level (10–50 parts per hundred parts of rubber, phr) on the final properties and structural changes of NR composites. The results indicated that increased filler loading led to higher curing torques and stiffness of the rubber composites irrespective of the type of filler used. The better filler dispersion was achieved in composites filled with CaCO₃ which is responsible for less polarity of CaCO₃ compared to silica. Good filler distribution enhanced filler–matrix interactions, improving swelling resistance and total crosslink density, and delaying stress relaxation. The modulus and tensile strength of both composites also improved over the content of fillers. The CaCO₃-filled composites reached their maximum tensile strength at 40 phr, exceeding, by roughly 88%, the strength of an unfilled sample. Conversely, the maximum tensile strength of silica-filled NR was at 20 phr and was only slightly higher than that of its unfilled counterpart. This discrepancy was ascribed to the stronger rubber–filler interactions in cases with CaCO₃ filler. Effective rubber–filler interactions improved strain-induced crystallization, increasing crystallinity during stretching and reducing the strain at which crystallization begins. In contrast, large silica aggregates with poor dispersion reduced the overall crosslink density, and degraded the thermomechanical properties, tensile properties, and strain-induced crystallization ability of the NR. The results clearly indicate that CaCO₃ should be favored over silica as a filler in the production of some rubber products where high performance was not the main characteristic. Full article

Calcium carbonate (CaCO₃), a natural common inorganic material with good biocompatibility, low toxicity, pH sensitivity, and low cost, has a widespread use in the pharmaceutical and chemical industries. In recent years, an increasing number of CaCO₃-based nano-drug delivery systems have been developed. CaCO₃ as a drug carrier and the utilization of CaCO₃ as an efficient Ca²⁺ and CO₂ donor have played a critical role in tumor diagnosis and treatment and have been explored in increasing depth and breadth. Starting from the CaCO₃-based nano-drug delivery system, this paper systematically reviews the preparation of CaCO₃ nanoparticles and the mechanisms of CaCO₃-based therapeutic effects in the internal and external tumor environments and summarizes the latest advances in the application of CaCO₃-based nano-drug delivery systems in tumor therapy. In view of the good biocompatibility and in vivo therapeutic mechanisms, they are expected to become an advancing biomedicine in the field of tumor diagnosis and treatment. Full article

This study investigates the interaction of polyacrylamide (PAM) of different functional groups (sulfonate vs. carboxylate) and charge density (30% hydrolysed vs. 10% hydrolysed) with calcium carbonate (CaCO₃) via atomic force microscopy (AFM) and partly via molecular dynamic (MD) simulations. The PAM used were F3330 (30% hydrolysed), AN125 (25% sulfonated), and AN910 (% hydrolysed). A total of 100 ppm of PAMs was prepared in 0.1% NaCl, 3% NaCl, and 4.36% NaNO₃ to be employed in AFM experiments, while oligomeric models (30 repeating units) of hydrolysed polyacrylamide (HPAM), sulfonated polyacrylamide (SPAM), and neutral PAM (NPAM) were studied on a model calcite surface on MD simulations. AFM analysis indicated that F3330 has a higher average adhesion and interaction energy with CaCO₃ than AN125 due to the bulky sulfonate side group of AN125 interfering with SPAM adsorption. Steric repulsion of both PAMs was similar due to their comparable molecular weights and densities of the charged group. In contrast, AN910 showed lower average adhesion and interaction energy, along with slightly longer steric repulsion with calcite than F3330, suggesting AN910 adopts more loops and tails than the slightly flatter F3330 configuration. An increase in salt concentration from 0.1% to 3% NaCl saw a reduction in adhesion and interaction energy for F3330 and AN125 due to charge screening, while AN910 saw an increase, and these values increased further at 4.36% NaNO₃. MD simulations revealed that the salt ions in the system formed salt bridges between PAM and calcite, indicating that the adhesion and interaction energy observed from AFM are likely to be the net balance between PAM charged group screening and salt bridging by the salt ions present. Salt ions with larger bare radii and smaller hydrated radii were shown to form stronger salt bridges. Full article

Nanomaterials enhance the performance of both asphalt binders and asphalt mixtures. They also improve asphalt durability, which reduces resource consumption and environmental impact in the long term associated with the production and transportation of asphalt materials. Thus, this paper studies the effectiveness of Nano Calcium Carbonate (Nano CaCO₃) and Nano Hydrated Lime (NHL) as modifiers and examines their impact on ranges from 0% to 10% through comprehensive laboratory tests. Softening point, penetration, storage stability, viscosity, and mass loss due to short-term aging using the Rolling Thin Film Oven Test (RTFO) were performed on asphalt binders. Results indicated a significant improvement in binder stiffness, particularly at 4% Nano CaCO₃ and 6% NHL content by weight. Dynamic Shear Rheometer (DSR) tests further revealed substantial improvements in rutting resistance, with NHL exhibiting superior high-temperature stability and a notable increase in the rutting factor. Marshall stability tests on asphalt concrete (AC) mixtures showed a 22.3% increase in stability with 6% NHL by weight, surpassing the 20.2% improvement observed with Nano CaCO₃ and indicating enhanced load-bearing capacity. The resilient modulus of the mixtures consistently increased with the addition of NHL, suggesting improved durability in rutting. Moisture susceptibility tests revealed that NHL significantly enhances moisture resistance, exceeding the 80% TSR benchmark at just 2% content by weight and reaching an impressive 94.6% at 10% content by weight. In contrast, Nano CaCO₃ demonstrated a more gradual improvement, achieving an 88.2% TSR at 10% content. Furthermore, permanent deformation analysis indicated a 68.64% improvement in rutting resistance with 10% NHL content by weight, exceeding Nano CaCO₃’s improvement rate. Optimal fatigue resistance was achieved at 4% for Nano CaCO₃ and 6% for NHL by weight, with respective CT index improvements of 30% and 35.4%, showing NHL’s consistent benefits across various nanomaterial contents. Overall, the study suggests that both Nano CaCO₃ and NHL positively impact asphalt performance, with NHL offering more pronounced benefits across a range of properties. These findings provide valuable insights for pavement engineers and underscore NHL’s potential as an effective additive in asphalt mixture design. Real-world applications and validations are essential for a comprehensive understanding of these nanomaterials in practical pavement engineering scenarios. Full article

Grounded in the auspicious horizons of geological polymers as alternative replacements for Portland cement and aligned with the national endeavor of constructing an ecological civilization and harnessing solid waste as a resource, this study delves into the integration of nanostructured calcium carbonate (CaCO₃) into geological polymers derived from fly ash and manganese slag. Employing a comprehensive methodology involving modalities, such as X-ray diffraction, scanning electron microscopy, and attenuated total reflectance Fourier-transform infrared spectroscopy, the influence of nano-CaCO₃ on the compressive strength, pore architecture, and polymerization degree of geological polymers is meticulously unveiled. The outcomes reveal that nano-CaCO₃ adeptly infiltrates the intricate microporous architecture of geological polymers, thereby providing a compact and intrinsically reinforcing matrix, ultimately endowing a marked increase in compressive strength. The assimilation of nano-CaCO₃ correlates conspicuously with an increase in monomeric calcium concentrations, thereby catalyzing and expediting the formation of polymeric assemblages within the system, which in turn accelerates the progression of geological polymerization. This catalytic effect augments the intricate three-dimensional lattice-like gel structures, consequently orchestrating a substantial amelioration in mechanical attributes. When the dosage of nano-CaCO₃ was 3.5%, sodium silicate was 10%, and NaOH was 12%, the integrated performance of fly ash–Mn slag geopolymer was optimal. Specifically, the 28-day compressive strength reached 25.6 MPa, and the compressive strength of the weathering performance test increased by 8.31%. The polymer achieved 96.77% curing of Mn, and it was non-radioactive. Thus, the prepared geopolymers are safe and reliable and support the subsequent development of nanomaterial activators. Full article

Composite powders were synthesized from the water solutions of sodium silicate and different calcium salts (nitrate, chloride, and acetate) at a Ca/Si molar ratio of 1.0. According to the XRD data, all the synthesized powders included hydrated calcium silicate Ca_1,5SiO_3,5·xH₂O (Ca/Si molar ratio = 1.5) and calcium carbonate CaCO₃ (Ca/Si molar ratio = ∞). The presence of H₂SiO₃ or SiO₂·xH₂O in the synthesized powders was assumed to be due to the difference between the Ca/Si molar ratio of 1.0 specified by the synthesis protocol and the molar ratio of the detected products. Reaction by-products (sodium nitrate NaNO₃, sodium chloride NaCl, and sodium acetate NaCH₃COO) were also found in the synthesized powders after filtration and drying. According to the XRD data phase composition of all powders after washing four times consisted of the quasi-amorphous phase and calcium carbonate in the form of calcite. Calcium carbonate in the form of aragonite was detected in powders synthesized from calcium chloride CaCl₂ and calcium nitrate Ca(NO₃)₂ before and after washing. Synthesized powders containing reaction by-products and washed powders were used for the preparation of ceramics at 900, 1000, and 1100 °C. The phase composition of the ceramic samples prepared from the washed powders and powder containing NaCl after firing at 900 and 1000 °C consisted of β-wollastonite β-CaSiO₃, and, after firing at 1100 °C, consisted of both β-wollastonite β-CaSiO₃ and pseudo-wollastonite α-CaSiO₃. The phase composition of the ceramic samples prepared from powders containing sodium nitrate NaNO₃ and sodium acetate NaCH₃COO after firing at 900, 1000, and 1100 °C consisted of calcium sodium silicates, i.e., Na₂Ca₂Si₃O₉ (combeite) and Na₂Ca₃S_i2O₈. Synthesized and washed composite powders can be used for the preparation of biocompatible materials, in the technology of construction materials, and as components of lunar soil simulants. Full article