In this work, a composite spherical adsorbent, which employs potassium titanium silicate as an adsorption active component, and calcium alginate as a carrier, was successfully prepared. Scanning electron microscopy (SEM) and energy dispersive spectroscopy (EDS) were used to characterize the adsorbent. The kinetics and thermodynamics of rubidium and cesium ions adsorption were investigated comprehensively, by considering the effects of initial concentration, temperature, solution pH, and coexisting NaCl. According to the determination coefficients, the pseudo second-order kinetic model provided an impressive and comparable correlation, and the second-order rate constant and the initial adsorption rate increase with increasing temperature. In general, the equilibrium adsorption amount increases with the increasing initial metal ion concentration, but decreases with increasing coexisting NaCl. The adsorption capacity keeps constant in the pH value range 3-12 and slightly fades when the temperature increases from 25 to 55°C. Under similar conditions, rubidium and cesium show the similar adsorption amount. The adsorbent has a fast adsorption rate and an adsorption capacity of about 1.55 mmol g−1 for rubidium and 1.47 mmol g−1 for cesium when the initial metal ion concentration is 0.10 mol L−1. The composite adsorbent is effective for the adsorption of rubidium or cesium ions from simulated brines.
A simple and practical spray method is employed to prepare a PVDF/PFOTES-SiO2 superhydrophobic composite coating on the AZ31B Mg alloy substrate. The morphology, composition, and water contact angle (CA) were measured by Fourier transform infrared spectroscopy (FTIR), field emission scanning electron microscope (FESEM) and contact angle measuring instrument. Hydrophilic nano-SiO2 is modified by PFOTES to obtain hydrophobicity. The influence of the mass of PFOTES-SiO2 to PVDF on the hydrophobic properties was studied. The wear resistance and stability of the composite coating have been investigated by immersion test, cross-cut adhesion test and friction test. Additionally, the corrosion resistance was measured by electrochemical workstation and salt spray corrosion test. The CA of PVDF/PFOTES-SiO2 coating is 161.3° and the sliding angle (SAs) is less than 2°. After 10× the sandpaper friction test, the superhydrophobic contact angle of the coating remained above 155°, and the sliding angle was less than 5°, which indicated that the prepared coating is a strong superhydrophobic coating with good wear resistance. The results of the electrochemical tests show that the superhydrophobic coating improved the anti-corrosion performance of Mg alloy, and the water contact angle is greater than 150° after 168 h salt spray corrosion test. Due to its excellent superhydrophobicity, wear resistance and anti-corrosion properties, the robust PVDF/PFOTES-SiO2 coating is considered to have great potential for future applications in the automotive and marine industries.