Search

Hydrophobic fibrous slippery liquid-infused porous surfaces (SLIPS) were fabricated by electrospinning polydimethylsiloxane (PDMS) and polystyrene (PS) as a carrier polymer on plasma-treated polyethylene (PE) and polyurethane (PU) substrates. Subsequent infusion of blackseed oil (BSO) into the porous structures was applied for the preparation of the SLIPS. SLIPS with infused lubricants can act as a repellency layer and play an important role in the prevention of biofilm formation. The effect of polymer solutions used in the electrospinning process was investigated to obtain well-defined hydrophobic fibrous structures. The surface properties were analyzed through various optical, macroscopic and spectroscopic techniques. A comprehensive investigation of the surface chemistry, surface morphology/topography, and mechanical properties was carried out on selected samples at optimized conditions. The electrospun fibers prepared using a mixture of PDMS/PS in the ratio of 1:1:10 (g/g/mL) using tetrahydrofuran (THF) solvent showed the best results in terms of fiber uniformity. The subsequent infusion of BSO into the fabricated PDMS/PS fiber mats exhibited slippery behavior regarding water droplets. Moreover, prepared SLIPS exhibited antibacterial activity against Staphylococcus aureus and Escherichia coli bacterium strains. [ABSTRACT FROM AUTHOR]

In this paper, diffuse coplanar surface barrier discharge plasma at atmospheric pressure has been used for surface modification of polyester/cotton (PESc) fabric, which was subsequently modified by sol–gel process using suitable organofunctional silanes to enhance its hydrophobicity. Modified PESc fabric surfaces were conditioned during the gelling process to obtain the permanent hydrophobicity. The contact angle of water before washing of plasma and sol–gel pretreated PESc fabric was found to be 154° and 151° after standardized washings. It was also demonstrated that the process is applicable at the industrial scale. [ABSTRACT FROM AUTHOR]

The massive increase in the volumes of oily contaminated produced waters associated with various industrial sectors has initiated considerable technological and scientific efforts related to the development of new cleaning strategies. The petrochemical industry (oil and gas production and processing) contributes to those volumes by approximately 340 billion barrels per year. The removal of emulsified oily components is a matter of particular interest because the high emulsion stability necessitates sophisticated technological approaches as well as a deep theoretical understanding of key mechanisms of oil/water separation. This review deals with the theoretical aspects of the treatment of emulsified oil/water mixtures and is particularly focused on tertiary treatment, which means the reduction of the oil content from 70–100 ppm to below 10 ppm, depending on national regulations for water discharge. The review concerns the mechanisms of oil/water separation and it covers the (i) adsorption isotherms, (ii) kinetics of adsorption, (iii) interfacial interactions between oil/water mixtures and solid surfaces, and (iv) oil/water separation techniques based on the wettability of solid/oil/water interfaces. The advantages and drawbacks of commonly used as well as newly proposed kinetic and adsorption models are reviewed, and their applicability for the characterization of oil/water separation is discussed. The lack of suitable adsorption isotherms that can be correctly applied for a description of oil adsorption at external and internal solid surfaces of both nonporous and porous structures is pointed out. The direct using of common isotherms, which were originally developed for gas adsorption, often leads to the incorrect data description because the adsorption of oily components at solid surfaces does not fit the assumptions from which these models were originally derived. Particularly, it results in problematic calculations of the thermodynamic parameters of sorption. The importance of nonlinear analysis of data is discussed, since recent studies have indicated that the error structure of experimental data is usually changed if the original nonlinear adsorption isotherms are transformed into their linearized forms. The comparison between the pseudo-first-order and pseudo-second-order kinetic models was performed. It was shown that the correlation between data and models strongly depends on the selection of data, particularly on the frequency of collected data in time scale. The wettability of solid surfaces by oil in air and under water is discussed, regarding the surface morphology of surfaces. We demonstrate that the combination of surface chemistry and topology strongly influences the separation of oil/water emulsions. [ABSTRACT FROM AUTHOR]

Herein, the surface treatment of polyurethane (PU) films via air, O2, N2, Ar, and their mixtures were tested. The treatment was performed to incorporate new polar functionalities on the polymer surface and achieve improved hydrophilic characteristics. The PU films were subjected to RF low-temperature plasma treatment. It was found that plasma treatment immensely enhanced the hydrophilic surface properties of the PU films in comparison with those of the pristine samples; the maximum plasma effect occurred for the PU sample in the presence of air plasma with treatment time of 180 s at nominal power of 80 W. The surface topography was also found to vary with plasma exposure time and the type of gas being used due to the reactivity of the gaseous media. Roughness analysis revealed that at higher treatment times, the etching/degradation of the surface became more pronounced. Surface chemistry studies revealed increased O2 and N2 elemental groups on the surface upon exposure to O2, N2, air, and Ar. Additionally, the aging study revealed that samples treated in the presence of air and Ar were more stable in comparison to those of the other gases for both the contact angle and peel test measurements. [ABSTRACT FROM AUTHOR]

The use of polymers in all aspects of daily life is increasing considerably, so there is high demand for polymers with specific properties. Polymers with antibacterial properties are highly needed in the food and medical industries. Low-density polyethylene (LDPE) is widely used in various industries, especially in food packaging, because it has suitable mechanical and safety properties. Nevertheless, the hydrophobicity of its surface makes it vulnerable to microbial attack and culturing. To enhance antimicrobial activity, a progressive surface modification of LDPE using the antimicrobial agent grafting process was applied. LDPE was first exposed to nonthermal radio-frequency (RF) plasma treatment to activate its surface. This led to the creation of reactive species on the LDPE surface, resulting in the ability to graft antibacterial agents, such as ascorbic acid (ASA), commonly known as vitamin C. ASA is a well-known antioxidant that is used as a food preservative, is essential to biological systems, and is found to be reactive against a number of microorganisms and bacteria. The antimicrobial effect of grafted LDPE with ASA was tested against two strong kinds of bacteria, namely, Staphylococcus aureus (S. aureus) and Escherichia coli (E. coli), with positive results. Surface analyses were performed thoroughly using contact angle measurements and peel tests to measure the wettability or surface free energy and adhesion properties after each modification step. Scanning electron microscopy (SEM) and atomic force microscopy (AFM) were used to analyze the surface morphology or topography changes of LDPE caused by plasma treatment and ASA grafting. Surface chemistry was studied by measuring the functional groups and elements introduced to the surface after plasma treatment and ASA grafting, using Fourier transform infrared (FTIR) spectroscopy and X-ray photoelectron spectroscopy (XPS). These results showed wettability, adhesion, and roughness changes in the LDPE surface after plasma treatment, as well as after ASA grafting. This is a positive indicator of the ability of ASA to be grafted onto polymeric materials using plasma pretreatment, resulting in enhanced antibacterial activity. [ABSTRACT FROM AUTHOR]

[Display omitted] • Electrochemical activation by ORR of commercial tungsten carbide was done. • Induction of oxycarbides species on surface activated WC material. • In-situ study identified improvement inchemisorption. • Enhanced electrocatalytic performance achieved by processing activation. The chemistry of electrocatalysts deals with multiple critical factors to facilitate the electrochemical reactions. Among those, the rate limiting depends on electrons transfer for chemisorptions of molecules in redox reactions. This feature can be directly linked with efficient catalyst support material in electrocatalysis. To this end, we have developed a novel, simple and facile route to introduce commercially available material with tuned surface and interface chemistry for their potential applications in fuel cells (FCs) science and technology. Commercial tungsten carbide (WC) was activated by means of electrochemical oxygen reduction reactions (ORR) on different rotation rates to induce mild interactions of oxygen molecules with surface of WC at specified reduction potentials. The X-ray diffraction and X-ray photoelectron spectroscopy analysis before and after the activation confirmed the tuning of WC surface with incorporation of potential factors to activate them for enhanced electrocatalytic activities. In addition, the electrocatalytic methanol oxidation reactions (MOR) and hydrogen evolution reactions (HER) were carried and confirmed the exceptional boosted-up electrocatalytic behaviour of WC after the activation. The enhancement in electrocatalytic mechanism after activation was also tested and proved by means of in-situ FTIR spectroelectrochemical analysis for methanol electro-oxidation. In addition, the electrochemical depositions of Pt nanoparticles were carried out on WC surface before and after the activation to reveal the influence of surface activation for accommodating the foreign particles as support material in electrocatalysis. The results shown two fold enhancement in anodic performance of Pt-modified activated WC catalyst for methanol oxidation reactions and hydrogen evolution reactions in fuel cells. [ABSTRACT FROM AUTHOR]