Silver nanoparticle thin layers were deposited onto formaldehyde-radio frequency (RF)-plasma-functionalized medical-and food-grade silicone rubber, stainless steel, and paper surfaces. The silver deposition was carried out under ex situ plasma conditions using the Tollen's reaction. Results from survey and high-resolution electron spectroscopy for chemical analysis, scanning electron microscopy (SEM), atomic force microscopy (AFM), and energy dispersive X-ray spectroscopy investigations confirmed the presence of thin silver layers on the plasma-exposed and subsequently modified substrate surfaces. In addition, SEM and AFM demonstrated the nanoparticle-based morphology of the deposited layers. Our results showed that thin macromolecular layers bearing aldehyde functionalities can be deposited onto silicone rubber, stainless steel, and paper surfaces. The bactericidal properties of the silver-coated surfaces were demonstrated by exposing them to Listeria monocytogenes. No viable bacteria were detected after 12 to 18 h on silver-coated silicone rubber surfaces.
A simple cold plasma technique was developed to functionalize the surfaces of polyamide (PA) and polyester (PET) for the grafting of polyethylene glycol (PEG) with the aim of reducing biofilm formation. The surfaces of PA and PET were treated with silicon tetrachloride (SiCl4) plasma, and PEG was grafted onto plasma-functionalized substrates (PA-PEG, PET-PEG). Different molecular weights of PEG and grafting times were tested to obtain optimal surface coverage by PEG as monitored by electron spectroscopy for chemical analysis (ESCA). The presence of a predominant C-O peak on the PEG-modified substrates indicated that the grafting was successful. Data from hydroxyl group derivatization and water contact angle measurement also indicated the presence of PEG after grafting. The PEG-grafted PA and PET under optimal conditions had similar chemical composition and hydrophilicity; however, different morphology changes were observed after grafting. Both PA-PEG and PET-PEG surfaces developed under optimal plasma conditions showed about 96% reduction in biofilm formation by Listeria monocytogenes compared with that of the corresponding unmodified substrates. This plasma functionalization method provided an efficient way to graft PEG onto PA and PET surfaces. Because of the high reactivity of Si-Cl species, this method could potentially be applied to other polymeric materials.
Polyethylene glycol (PEG) structures were deposited onto stainless steel (SS) surfaces by spin coating and argon radio frequency (RF)-plasma mediated crosslinking. Electron spectroscopy for chemical analysis (ESCA) and attenuated total reflectance Fourier transform infrared spectroscopy (ATR-FTIR) indicated the presence of -CH 2 -CH 2 -O-structure and C-C-C linkage, as a result of the plasma crosslinking, on PEG-modified SS surfaces. Scanning electron microscopy (SEM) indicated complete deposition, and water contact angle analysis revealed higher hydrophilicity on PEG-modified surfaces compared to unmodified SS surfaces. Surface morphology and roughness analysis by atomic force microscopy (AFM) revealed smoother SS surfaces after PEG modification. The evaluation of antifouling ability of the PEG-modified SS surfaces was carried out. Compared to the unmodified SS, PEG-modified surfaces showed about 81-96% decrease in Listeria monocytogenes attachment and biofilm formation (p Ͻ 0.05). This cold plasma mediated PEG crosslinking provided a promising technique to reduce bacterial contamination on surfaces encountered in food-processing environments.
Plasma treatment of contaminated water appears to be a promising alternative for the oxidation of aqueous organic pollutants. This study examines the kinetic and oxidation mechanisms of methyl tert-butyl ether (MTBE) in a dense medium plasma (DMP) reactor utilizing gas chromatography-mass spectrometry and gas chromatography-thermal conductivity techniques. A rate law is developed for the removal of MTBE from an aqueous solution in the DMP reactor. Rate constants are also derived for three reactor configurations and two pin array spin rates. The oxidation products from the treatment of MTBE-contaminated water in the DMP reactor were found to be predominately carbon dioxide, with smaller amounts of acetone, tert-butyl formate, and formaldehyde. The lack of stable intermediate products suggests that the MTBE is, to some extent, oxidized directly to carbon dioxide, making the DMP reactor a promising tool in the future remediation of water. Chemical and physical mechanisms together with carbon balances are used to describe the formation of the oxidation products and the important aspects of the plasma discharge.
ABSTRACT:Chopped sisal fibers and finely powdered high-density polyethylene were surface functionalized using dichlorosilane (DS) under radio frequency (RF)-plasma conditions and characterized by electron spectroscopy for chemical analysis (ESCA) and fluorescence labeling techniques. A high-capacity (10 L), rotating, 13.56 MHz, electrodeless plasma installation, specially designed to allow the uniform surface modification of powdery and particulate matter of irregular shape, was used. A three-factor fractional experimental design was employed to evaluate the effect of RF-power, pressure, and reaction time on the ESCA-based relative atomic composition of plasmatreated samples. It was demonstrated that OSiH x Cl y functionalities are present on plasma-exposed surfaces and these functionalization reactions can be controlled by selecting proper plasma parameters.
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