ABSTRACT
The present work reports on the fabrication of high-density polyethylene sponges, decorated with Mn-doped ZnO nanostructures. The sponges were developed utilizing three-dimensional printing technology, while Mn-doped ZnO nanostructures, with varying doping levels, were grown at mild temperatures. The nanostructures were fully characterized by means of scanning electron microscopy, X-ray diffraction, and Raman spectroscopy, revealing the existence of Mn doping. Moreover, their photocatalytic properties were investigated using the degradation/decolorization of a commercially available liquid laundry detergent, based on synthetic, less foaming ingredients, under UV irradiation. The Mn-doped ZnO nanostructures show better photocatalytic activity at higher doping levels. This study demonstrates that it is possible to achieve the adequate degradation of a typical detergent solution in water by means of low-cost and environmentally friendly approaches, while Mn-doped ZnO/HDPE nanostructures are good candidates for real environmental applications.
ABSTRACT
The development of a superhydrophobic and, even, water-repellent metal alloy surface is reported utilizing a simple, fast, and economical way that requires minimum demands on the necessary equipment and/or methods used. The procedure involves an initial irradiation of the metallic specimen using a femtosecond laser, which results in a randomly roughened surface, that is subsequently followed by placing the item in an environment under moderate vacuum (pressure 10-2 mbar) and/or under low-temperature heating (at temperatures below 120 °C). The effects of both temperature and low pressure on the surface properties (water contact angle and contact angle hysteresis) are investigated and surfaces with similar superhydrophobicity are obtained in both cases; however, a significant difference concerning their water-repellent ability is obtained. The surfaces that remained under vacuum were water-repellent, exhibiting very high values of contact angle with a very low contact angle hysteresis, whereas the surfaces, which underwent thermal processing, exhibited superhydrophobicity with high water adhesion, where water droplets did not roll off even after a significant inclination of the surface. The kinetics of the development of superhydrophobic behavior was investigated as well. The findings were understood when the surface roughness characteristics were considered together with the chemical composition of the surface.
ABSTRACT
Dynamic light scattering, potentiometric titration, transmission electron microscopy and atomic force microscopy have been used to investigate the micellar behaviour and metal-nanoparticle formation in poly(ethylene oxide)-block-poly(2-vinylpyridine), PEO-b-P2VP, poly(hexa(ethylene glycol) methacrylate)-block-poly(2-(diethylamino)ethyl methacrylate), PHEGMA-b-PDEAEMA, and PEO-b-PDEAEMA amphiphilic diblock copolymers in water. The hydrophobic block of these copolymers (P2VP or PDEAEMA) is pH-sensitive: at low pH it can be protonated and becomes partially or completely hydrophilic leading to molecular solubility whereas at higher pH micelles are formed. These micelles consist of a P2VP or PDEAEMA core and a PEO or PHEGMA corona, respectively, where the core forming amine units can incorporate metal compounds due to coordination. The metal compounds (e.g., H2PtCl6, K2PtCl6) can either be introduced in a micellar solution, where they are incorporated within the micelle core via coordination with functional groups, or can be added to a unimer solution at low pH, where they lead to a metal-induced micellization. In these micellar nanoreactors, metal nanoparticles nucleate and grow upon reduction with sizes in the range of a few nanometers as observed by TEM. The effect of the metal incorporation method on the characteristics of the micelles and of the synthesized nanoparticles is investigated.
