The key reactive species generated by non-thermal plasma bubbles for the inactivation of Salmonella Typhimurium and the effects of organic matter on the inactivation efficacy were investigated. Plasma, which is primarily composed of ozone (O₃), was generated by dielectric barrier discharge and injected into a solution (400 mL) as a bubble. The surviving population of S. Typhimurium decreased in proportion to the treatment time, resulting in a 5.29 log reduction after 5 min of treatment. Verification tests to specify key reactive species were conducted using an O₃ destruction unit and reactive oxygen species scavengers. The results indicated that singlet oxygen (¹O₂) contributes substantially to the inactivation of S. Typhimurium, and that the presence of superoxide anion radicals (O₂^·−) from O₃ is essential for the production of ¹O₂. When a S. Typhimurium suspension containing organic matter (final concentration: 0, 0.005, 0.05, 0.1, and 0.5 g/L), consisting of beef extract and peptone, was treated with plasma bubbles for 5, 10, 15, 20, 25, and 30 min, respectively, the potential of the plasma bubbles for inactivating S. Typhimurium successfully was verified with longer contact time, despite organic matter attenuating the inactivation efficiency in a dose-dependent manner.

This study investigated the optimum conditions to maximize the inactivation of biofilms using both plasma-treated solutions and post-treatment storage conditions. Chemical properties of plasma-treated solutions were also analyzed to identify their possible biofilm inactivation mechanisms. Escherichia coli O157:H7 biofilms on stainless steel were prepared and immersed in distilled water (DW), 100 ppm of sodium chloride solution (NaCl), or 100 ppm of sodium hypochlorite solution (NaOCl), followed by container-type plasma treatment for 10 min (15 kHz and 250 W). After plasma discharge was switched off, biofilms immersed in the plasma-treated solution were stored for 10 min with the plasma apparatus closed or open. The log reduction of E. coli O157:H7 was NaOCl (3.58) > NaCl (2.06) = DW (1.95) in the closed storage condition. In addition, the bactericidal effect of NaOCl was higher in the closed condition than in the open condition. Concentrations of the hydroxyl radical (OH·) and peroxynitrite (ONOO⁻) were also the highest for NaOCl in the closed condition. Consequently, plasma treatment using NaOCl solution in the closed condition was found to be the optimum method for inactivation of E. coli O157:H7 biofilms, due to high hydroxyl radical and peroxynitrite concentrations. This method also has the merit of using a lower concentration of NaOCl than that used typically in industry.

With the spread of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), disease prevention has become incredibly important. Consequently, mask and air-purifier use has increased. The filter is the core component of these items. However, most filter materials lack antimicrobial properties. Copper is a sustainable antimicrobial material. When copper is deposited onto the filter’s surface, the microorganisms that come into contact with it can be effectively inactivated. In this study, we used an oxygen ion beam with a controlled process temperature to treat filter surfaces with copper. This enabled a strong adhesion of at least 4 N/cm between the copper and the filter fibers without damaging them. Upon exposing the filter to bacteria (Staphylococcus aureus ATCC 6538, Klebsiella pneumoniae ATCC 4352, Escherichia coli ATCC 25922, and Pseudomonas aeruginosa ATCC 27853) for one hour, a >99.99% removal rate was attained; when the filter was exposed to SARS-CoV-2 virus for one hour, it inactivated more than 99%. These beneficial properties minimize the risk of secondary infections, which are significantly more likely to occur when a conventional filter is replaced or removed.

Optical emission spectral tomography diagnostics have been developed to measure the spatial uniformity of meter-sized processing plasmas. The lines of sight and detector location are selected based on tomographic reconstruction tests using synthetic (phantom) images. The developed collection optics system is composed of slits, a plano-convex lens, optical interference filters and photodiode arrays. Using the collection optics, the line-integrated emission intensity is acquired from a meter-sized rectangular argon plasma (inductively coupled plasma at a frequency of 13.56 MHz), which was developed for display panel manufacturing. From the measured intensity, two-dimensional (2D) spatial distributions of argon atomic line intensity (675.3 nm and 852.1 nm) are obtained via the tomographic reconstruction technique based on the Phillips–Tikhonov regularization. In addition, 2D profiles of the electron excitation temperature ( T _exc ) are obtained from those of Ar intensity at the wavelengths 675.3 nm and 852.1 nm via two line method (in essence, a Boltzmann plot). The 2D argon plasma emission and T _exc profiles match well with the shape of the electrode and etch rate profile.

Plasma‐facing liquids (PFLs) facilitate the storage of reactive O and N species (RONS), including H₂O₂ and NO₂⁻, which remain in the PFL after plasma treatment, and they can continuously influence the target immersed in the liquid. However, their behaviors and levels of generation and extinction depend strongly on the plasma characteristics and liquid condition. Therefore, understanding the effects of the liquid type on the plasma discharge characteristics and the RONS generated via plasma discharge is necessary. We compared the RONS generation and storage trends of deionized H₂O and a high‐conductivity PFL, RPMI 1640, which is a well‐known cell culture medium commonly used to culture mammalian cells. RPMI 1640 acted as an electrode and enhanced the plasma discharge power by supplying abundant radicals and RONS. The production of gaseous hydroxyl radicals and NO markedly increased, which facilitated H₂O₂ and NO₂⁻ production in the PFL for the first 200 s, and then the increase in the RONS concentration stagnated. With respect to storage, as the components within RMPI 1640 exhibited high reaction constants for their reactions with H₂O₂, H₂O₂ elimination was completed in <30 min. Unlike H₂O₂, the concentration of NO₂⁻ in the PFL was unchanged.