Search

In the context of escalating global efforts to mitigate carbon emissions and explore sustainable energy resources, the transformation of CO2 into valuable chemicals and fuels via plasma technology has garnered significant attention. This study demonstrated a new pathway of CO2 conversion into CO and H2O2 via the bubble-enabled gas-liquid discharge driven by a nanosecond pulse. Results showed that the increased discharge frequency and larger pulse widths could enhance CO2 conversion rates and H2O2 yields, albeit potentially at the cost of reduced energy efficiency. Conversely, the rising time of pulse showed negligible impact on the process, whereas varying gas flow rates significantly altered CO and H2O2 yields, underscoring the nuanced influence of these parameters on the efficiency and selectivity of conversion processes. Through illuminating the dynamics of bubble discharge-assisted CO2 transformation, this study contributes to the broader understanding of gas-liquid discharge driven by nanosecond pulse, underlining its potential for addressing environmental and energy challenges. [ABSTRACT FROM AUTHOR]

Non-thermal plasma coupling with photocatalyst is recognized as a promising technology for the degradation of antibiotics, and improving the photocatalyst performance is one of the most significant strategies to improve the efficiency of plasma-catalytic systems. This study employed a nanosecond pulsed gas–liquid discharge coupled with plasma-functionalized TiO2 to achieve a high efficiency of tetracycline degradation and clarify the synergistic mechanism of nanosecond pulse discharge coupling with functionalized TiO2. Results showed that the degradation efficiency with functionalized TiO2 increased by 20% compared to the untreated TiO2 for 4 min-plasma treatment. It is also suggested that the effect of photogenerated holes and electrons can be promoted in the functionalized TiO2, as evidenced by the radical quenching experiments. The plasma-modified TiO2 catalysts were proven to have a good stability and recyclability. This study provides a new sustainable approach to enhance the performance of photocatalysts in the plasma system for environmental remediation. [ABSTRACT FROM AUTHOR]

Plasma-activated hydrogels have promising application prospects in the field of transdermal penetration therapy, such as subcutaneous tumours, due to their long-lasting, slow-release properties and ability to be easily applied to skin. In this study, surface air plasma was used to prepare plasma-activated Aristoflex AVC hydrogel (PAH) and plasma-activated water (PAW) by irradiation. The characteristics of PAH and PAW were further studied in terms of reactive oxygen species (ROS) storage, transdermal permeation, and in vitro anticancer effects in an artificial skin model. The experimental results showed that PAH had a prolonged storage time of ROS and more transdermal permeation of ROS through artificial skin in Franz diffusion cell after 30 h compared to PAW, which means PAH could be superior to PAW for long-term applications on the skin surface. The in vitro anticancer effects of PAH in an artificial skin model were also better than those of PAW, reducing the viability of A375 cells without causing damage to HaCaT cells. Our study shows that PAH is superior to PAW in body-surface coating applications and can be used for subcutaneous anticancer applications. [ABSTRACT FROM AUTHOR]

Plasma-activated water (PAW) represents a promising green antibacterial agent for biomedical and agricultural applications. In this study, a novel AC multi-needle-to-water discharge device was developed to investigate the effects of gas flow on the generation and chemical composition of PAW. It is shown that the concentrations of and N(III) (and) in the PAW both increased with an extension of the plasma-processing time and a reduction of the gas-flow rate. The absorption of gas-phase products carried by the gas flow from the discharge chamber was found to be beneficial for the generation of both and N(III) in the PAW at a gas flow rate of 20–60 L h−1, yet their concentrations were still lower than those without any feeding gas. As opposed to or N(III), the concentration in the plasma-activated phosphate buffer solution (PAPBS) increased under stronger gas flows and was almost unaffected by absorption in PAPBS. The pH value of PAW increased at higher gas flow rates. A comparison of the N(III) in PAW and PAPBS reflects the effects of the reactions of and in the two different working liquids. To quantify the effects of gas flow on the discharge characteristics, gas temperatures were calculated from the optical emission spectra and were proven to be flow-independent near the discharge channel. Fourier transform infrared (FTIR) measurements of the gaseous products during the discharge, and further analysis of possible reaction pathways indicated that by controlling the gas flow in the multi-needle-to-water discharge system, the concentration of long-lived species in PAW could be tuned, which might favor the generation of These findings contribute to a better understanding of effective electric discharge-related mechanisms for enhancing the biochemical and chemical activities of PAW. [ABSTRACT FROM AUTHOR]

Novel plasma-based technologies that offer maximum efficiency at minimal environmental costs are expected to further promote the sustainable societal and economic development. Unique transfer of chemical reactivity and energy from gaseous plasmas to water takes place in the absence of any other chemicals, but results in a product with a notable transient broad-spectrum biological activity, referred to as plasma-activated water (PAW). These features make PAW a green prospective solution for a wide range of biotechnology applications, from water purification to biomedicine. Here, we present a succinct review of how novel, efficient methods based on non-equilibrium reactive plasma chemistries can be applied to low-cost natural water sources to produce a prospective product with a wide range of applications while at the same time minimising the process steps and dramatically reducing the use of expensive and/or hazardous reagents. Despite the recent exciting developments in this field, there presently is no topical review which specifically focuses on the underlying physics and chemistry related to plasma-activated water. We focus specifically on the PAW generation, origin of reactive species present in PAW, its related analytical chemistry and potentially different mechanisms that regulate the bio-activities of PAW in different biotech-applications and their roles in determining PAW efficacy and selectivity. We then review recent advances in our understanding of plasma-water interactions, briefly outlining current and proposed applications of PAW in agriculture, food and biomedicine. Finally, we outline future research directions and challenges that may hinder translation of these technologies into real-life applications. Overall, this review will provide much needed insights into the fundamental aspects of PAW chemistry required for optimization of the biochemical activity of PAW and translation of this environment- and human-health-friendly, and energy-efficient strategy into real life applications. [ABSTRACT FROM AUTHOR]