ABSTRACT
The present study investigates the impact and freezing behavior of the droplets of surfactant solutions on non-wettable coatings at very low temperatures of -10 to -30 °C. Our goal is to elucidate the critical role of concentration, molecular weight, and ionic nature of surfactants on these phenomena. To achieve this goal, we used sodium dodecyl sulfate (anionic), hexadecyltrimethylammonium bromide (cationic), and n-decanoyl-n-methylglucamine (nonionic) at four concentrations ranging from 0 to 2 × CMC (critical micelle concentration). We captured the impact-freezing of the droplets on superhydrophobic alkyl ketene dimer coatings using a high-speed camera at 5000 frames per second. The results show that the ability of the droplets to spread and retract on the coatings is a function of concentration, ionic nature, and molecular weight of the surfactants, as well as the temperature-dependent viscosity of the solutions. Additionally, surfactant-laden droplets generally demonstrated an accelerated freezing compared to pure water. This might be due to the fact that the presence of surfactants can promote both heterogeneous ice nucleation from within the liquid and a larger solid-liquid interfacial area by filling the air pockets of the surface, leading to enhanced heat transfer. The behavior of the cationic surfactant at certain concentrations was, however, an exception leading to a freezing delay, for which a mechanism will be proposed.
ABSTRACT
The addition of surfactants to pure water for specific applications has made controlling the impact dynamics of surfactant-laden droplets a complex phenomenon. This work investigates the influence of the molecular weight (MW), concentration, and ionic nature of the surfactants as well as the substrate surface characteristics on the impact dynamics of surfactant-laden droplets using a high-speed camera at 10â¯000 frames per second. Sodium dodecyl sulfate, hexadecyltrimethylammonium bromide, and n-decanoyl-n-methylglucamine were used as anionic, cationic, and nonionic surfactants, respectively. We used hydrophilic glass slides, hydrophobic polytetrafluoroethylene, and superhydrophobic alkyl ketene dimer (AKD) as substrates. The results show that the efficiency of the surfactant addition in increasing the maximum spreading diameter is significantly influenced by the molecular weight and ionic nature of the solutions as well as the nonwettability of the substrate. Among all of the surfaces examined, the concentration and ionic nature of the solutions were found to be more dominant parameters in determining the energy dissipation in the retraction phase of the droplet impact on the superhydrophobic AKD surfaces. As the concentration decreases or positive charges are present in the solution, it is more likely to observe a similar retraction dynamic to pure water when the droplet hits the superhydrophobic AKD having negatively charged surface sites. Finally, in terms of the impact outcomes of the surfactant-laden droplets on the superhydrophobic AKD, it is shown that the influence of the surfactant addition is more noticeable at lower Weber numbers, where the droplet tries to rebound by overcoming the energy loss that occurred in the spreading.
ABSTRACT
A new Fe3O4@SiO2 fluorescent probe for detection of Hg2+ in aqueous solutions was introduced based on a simple ligand. The prepared sample was characterized by using TEM, EDX, FT-IR, VSM, and TGA/DTA. The sensitivity of the probe toward Hg2+ and its selectivity in presence of other cations were proven by using fluorescence spectroscopy. The detection limit of the prepared chemosensor is 8.1 nM. The magnetic property of the prepared nanocomposite enables its separation by an external magnet. The simple structure of the employed ligand results in simple preparation procedure and therefore could be an applicable material for detection of Hg2+ in industrial, environmental, and biological samples.
ABSTRACT
HYPOTHESIS: Alkyl ketene dimer (AKD) is frequently used in paper industry as an inexpensive sizing agent. The formation of a porous structure after curing the solidified AKD for an extra-long time (4-6 days) results in superhydrophobicity. In this study, a facile and low-cost method was utilized to turn the surface of AKD superhydrophobic in a very short period of time. EXPERIMENTS: We fabricated superhydrophobic coatings by dipping glass and paper substrates in molten AKD and then treating them with ethanol after solidification. The samples were characterized by X-ray diffraction, Scanning electron microscopy, Fourier transform-infrared spectroscopy, X-ray photoelectron spectroscopy, Confocal laser scanning microscopy, and dynamic contact angle goniometry. FINDINGS: The results show that briefly treating the coatings, obtained from isothermally heated AKD melt at 40 °C for 3 min, with ethanol leads to superhydrophobicity with advancing and receding contact angles of 158.7 ± 1.4° and 156.8 ± 0.9°, respectively. By increasing the melt temperature to 70 °C and its heating time to 6 h followed by ethanol treatment, the advancing and receding contact angles increased to 163.7 ± 1.3° and 162.6 ± 1.2°, respectively. This enhancement in superhydrophobicity is due to the formation of porous, entangled irregular micro/nano textures that create air cushions on the surface resulting in droplet state transition from Wenzel to Cassie.
ABSTRACT
5-Amino-1,3,4-thiadiazole-2-thiol was used to synthesize a novel fluorescent functionalizing group on a Fe3O4@SiO2 magnetic nanocomposite surface for detection of heavy metal ions in water samples. The prepared probe was characterized by using X-ray diffraction, transmission electron microscopy, Fourier transform infrared spectroscopy, and a vibrating sample magnetometer. Among various tested ions, the new nanocomposite responded to Hg2+ ions with an intense fluorescence "turn-off". The limit of detection of the probe shows that it is sensitive to the minimum Hg2+ concentration of 48.7 nM. Theoretical calculations were done for estimating binding energies of the three possible bonding modes and the visualized molecular orbitals were presented.
ABSTRACT
In this work, two natural sources, including pomegranate peel extract and cochineal dye were employed for the synthesis of silver nanoparticles. The natural silver complex from pomegranate peel extract resulted in nano-sized structures through solution-phase method, but this method was not efficient for cochineal dye-silver precursor and the as-formed products were highly agglomerated. Therefore, an alternative facile solid-state approach was investigated as for both natural precursors and the results showed successful production of well-dispersed nanoparticles with narrow size distribution for cochineal dye-silver precursor. The products were characterized by X-ray diffraction (XRD), Scanning Electron Microscopy (SEM), Energy dispersive X-ray microanalysis (EDX), and Transmission Electron Microscopy (TEM).