RESUMO
The development of layered double hydroxide (LDH) nanosheets as nanocontainers has been intensively studied in recent years. Despite their potential for application on a large scale, their synthesis in an aqueous medium is rarely reported. Herein, we report a straightforward approach for the controllable synthesis of uniform MgAl-LDH nanosheets by an aqueous nucleation process followed by a hydrothermal treatment. The key to this method relies on the well-dispersed LDH nuclei that are produced by high-speed homogenization. Following the nucleation step, the coalescence of the aggregate hydroxide layers is diminished by hydraulic shear forces, leading to the disaggregation and even distribution of LDH nuclei. As a result, the oriented growth of individual crystals along the horizontal plane becomes predominant, leading to a high surface charge density of the hydroxide sheets and preventing their stacking. The electron microscope virtual proofs showed that the particles had a well-defined circular shape with a thickness of about 2-3 nm. Afterward, for the first time, LDH nanosheets were used to prepare LDH nanocontainers loaded with 2-benzothiazolythio-succinic acid (BTSA) by anion exchange. The incorporation of BTSA into the interlayer region and the emission behavior of the inhibitor were investigated. These results indicate that the prepared nanosheets can be utilized as effective nanocontainers for organic inhibitor loading and anti-corrosion application.
RESUMO
The innovative hollow silica nanoparticle (HSN) material possesses substantial potential for application in the insulation field. The size and shell thickness of HSN are crucial factors in determining their inherent properties, which, in turn, impact their applicability. This research presents a facile approach to synthesizing HSN in which sodium silicate (Na2SiO3) was utilized as the silica precursor that can be directly deposited onto layered double hydroxide (LDH) nanoparticles without the utilization of any surfactant. A subsequent acid treatment was used to eliminate the templates, resulting in the formation of an HSN devoid of mesopores in silica shells. By utilizing various sizes of LDH cores, obtainable via coprecipitation followed by hydrothermal treatment, we were capable of successfully synthesizing the hollow particles with adjustable diameters ranging from 50 to 200 nm. In addition, the shell thickness is varied from 6.8 to 22.5 nm by varying the silicate solution concentration. Results demonstrate that prepared HSNs have low thermal conductivity and high reflectance in the UV-vis-NIR range (averaging 82.1%). These findings suggest that HSN can be utilized as an effective inorganic filler in the formulation of reflective and thermally insulating coatings.
RESUMO
In this paper, a composite from polyaniline and graphene oxide-hydrotalcite hybrid (PAN-HG) was fabricated by direct polymerization of aniline using ammonium persulphate as an oxidant in the presence of a HG hybrid. The structure and morphological properties of synthesized PAN-HG composites were characterized by Fourier transform infrared (FTIR) spectroscopy, X-ray diffraction (XRD), Raman spectra, and scanning electron microscopy (SEM) techniques. The electrochemical properties of the composite particles were also analyzed by potentiodynamic polarization curves to evaluate the corrosion inhabitation. The results were calculated by Tafel fitting and showed that the effective corrosion protection values were 73.11%, 88.46%, and 95.49%, corresponding to HG, 1PAN-HG, and 2PAN-HG. The influence of PAN-HG on the corrosion protection of the polyurethane coating applied on the CT3 steel was investigated. As a result, the PU containing 0.5% of 2PAN-HG showed the most effective protection of the CT3 steel substrate. The R C of the coating was about 1.61 × 107 Ω cm2, and after immersion for 30 days, the R C value was 0.17 × 106 Ω cm2. From all the analyzed results, PAN-HG has enhanced the corrosion protection and a complicated protection mechanism was also concluded and explained.