Formation of Copper Oxide Nanotextures on Porous Calcium Carbonate Templates for Water Treatment

The necessity of providing clean water sources increases the demand to develop catalytic systems for water treatment. Good pollutants adsorbers are a key ingredient, and CuO is one of the candidate materials for this task. Among the different approaches for CuO synthesis, precipitation out of aqueous solutions is a leading candidate due to the facile synthesis, high yield, sustainability, and the reported shape control by adjustment of the counter anions. We harness this effect to investigate the formation of copper oxide-based 3D structures. Specifically, the counter anion (chloride, nitrate, and acetate) affects the formation of copper-based hydroxides and the final structure following their conversion into copper oxide nanostructures over porous templates. The formation of a 3D structure is obtained when copper chloride or nitrate reacts with a Sorites scaffold (marine-based calcium carbonate template) without external hydroxide addition. The transformation into copper oxides occurs after calcination or reduction of the obtained Cu2(OH)3X (X = Cl– or NO3–) while preserving the porous morphology. Finally, the formed Sorites@CuO structure is examined for water treatment to remove heavy metal cations and degrade organic contaminant molecules.

Barnase encapsulation into submicron porous CaCO3 particles – studies of loading and enzyme activity

The present study focuses on the immobilization of bacterial ribonuclease Barnase (Bn) into submicron porous calcium carbonate (CaCO3) particles. For encapsulation, we apply adsorption, freezing-induced loading and co-precipitation methods and...

Magneto-Fluorescent Hybrid Sensor CaCO3-Fe3O4-AgInS2/ZnS for the Detection of Heavy Metal Ions in Aqueous Media

Heavy metal ions are not subject to biodegradation and could cause the environmental pollution of natural resources and water. Many of the heavy metals are highly toxic and dangerous to human health, even at a minimum amount. This work considered an optical method for detecting heavy metal ions using colloidal luminescent semiconductor quantum dots (QDs). Over the past decade, QDs have been used in the development of sensitive fluorescence sensors for ions of heavy metal. In this work, we combined the fluorescent properties of AgInS2/ZnS ternary QDs and the magnetism of superparamagnetic Fe3O4 nanoparticles embedded in a matrix of porous calcium carbonate microspheres for the detection of toxic ions of heavy metal: Co2+, Ni2+, and Pb2+. We demonstrate a relationship between the level of quenching of the photoluminescence of sensors under exposure to the heavy metal ions and the concentration of these ions, allowing their detection in aqueous solutions at concentrations of Co2+, Ni2+, and Pb2+ as low as ≈0.01 ppm, ≈0.1 ppm, and ≈0.01 ppm, respectively. It also has importance for application of the ability to concentrate and extract the sensor with analytes from the solution using a magnetic field.

Removal of Phosphate from Aqueous Solutions Using Chemically Synthesized Vaterite Polymorph of Porous Calcium Carbonate Nanoparticles under Optimized Conditions

Eutrophication is one of the most adverse impacts of nutrient contamination of water bodies where the phosphate is considered to be the primary limiting factor. The vaterite polymorph of porous calcium carbonate nanoparticles (VPCCNPs) were synthesized and used to remove orthophosphate ions in water. In this study, the VPCCNPs were synthesized chemically, using calcium acetate and sodium bicarbonate in a water-ethylene glycol media, at a temperature of 100°C, in a reaction time of 24 hours. Synthesized nanoparticles were characterized by X-ray diffractometry to confirm that the crystalline phase of calcium carbonate formed is spherical vaterite polymorph. Scanning electron microscopy coupled with energy dispersive X-ray analysis further confirms the spherical shape of the vaterite nanoparticles and the presence of only calcium, carbon, and oxygen thus showing high purity of the synthesized calcium carbonate nanoparticles. The dynamic laser light scattering-based particle size analysis (DLS) shows the average particle size to be 25.5 nm. The Fourier transform infrared spectroscopy was used to find functional groups before and after the adsorption of phosphate by vaterite nanoparticles. The phosphate removal efficiency of synthesized nanoparticles was tested with different concentrations of phosphate solutions (2–80 mg/L), pH levels (5–12), adsorbent dosages (0.025–0.250 g), and contact times (5–120 min). Ion chromatography was used to analyse the phosphate concentrations in water samples. The maximum phosphate removal percentage of 100% was obtained with 50 mL of 2 mg/L phosphate solution and 0.15 g of the synthesized nanoparticle. Adsorption data were well fitted with the Langmuir adsorption isotherm model and the pseudo-second-order kinetic model with R2 of 0.99 and 0.98 (rate constant -0.083 g g-1 min-1), respectively. The presence of F−, NO3−, and SO42− has no effect on phosphate adsorption since 100% phosphate removal is obtained in the presence of these ions. Furthermore, the particle shows a 100% removal of orthophosphate ions available in eutrophic water regardless of the presence of many other ions in natural water bodies. The study presents a viable option for removing excess phosphate in natural water to desirable levels as a means for controlling eutrophication.

In Vitro and In Vivo Evaluation of Starfish Bone-Derived β-Tricalcium Phosphate as a Bone Substitute Material

We evaluated starfish-derived β-tricalcium phosphate (Sf-TCP) obtained by phosphatization of starfish-bone-derived porous calcium carbonate as a potential bone substitute material. The Sf-TCP had a communicating pore structure with a pore size of approximately 10 μm. Although the porosity of Sf-TCP was similar to that of Cerasorb M (CM)—a commercially available β-TCP bone filler—the specific surface area was roughly three times larger than that of CM. Observation by scanning electron microscopy showed that pores communicated to the inside of the Sf-TCP. Cell growth tests showed that Sf-TCP improved cell proliferation compared with CM. Cells grown on Sf-TCP showed stretched filopodia and adhered; cells migrated both to the surface and into pores. In vivo, vigorous tissue invasion into pores was observed in Sf-TCP, and more fibrous tissue was observed for Sf-TCP than CM. Moreover, capillary formation into pores was observed for Sf-TCP. Thus, Sf-TCP showed excellent biocompatibility in vitro and more vigorous bone formation in vivo, indicating the possible applications of this material as a bone substitute. In addition, our findings suggested that mimicking the microstructure derived from whole organisms may facilitate the development of superior artificial bone.