(Invited) Synthesis of Dinitrogen Pentoxide Using Air Atmospheric Pressure Plasmas and Application for Biomaterial Processes

Abstract

Atmospheric-pressure plasma (APP) technology, enabling to convert air molecules into multi-functional reactive species [e.g., reactive oxygen and nitrogen species (RONS)] with electricity, has been of great interest and extensively investigated. In particular, air APP devices, working only with air and electricity, can potentially allow for ubiquitous supply of RONS, which can be applied in a wide range of fields such as medical, agricultural, environmental, and biomaterial fields [1-4]. Recently, we have developed a new composite air APP device consisting low temperature and high temperature plasma reactors, enabling to supply RONS [e.g., dinitrogen pentoxide (N2O5), ozone (O3), nitric oxides (NOx), ...] with fine control and good reproducibility [5]. Specifically, its ability to generate high density (up to 200 ppm) N2O5 with high selectivity is quite unique and could accelerate scientific and industrial N2O5 applications. In addition, the APP device can utilize room air and renewable energy sources, such as a solar cell, and thus can realize sustainable and ubiquitous N2O5 supply.N2O5 is well known as a powerful oxidizing and nitrating agent and can potentially be bioactive. However, there are no previous studies using N2O5 in bio-applications, to our best knowledge. The reason is possibly due to its ordinary synthesis methods requiring multiple hazardous raw materials (requiring handling with much care). The air APP devices is user-friendly and can easily supply N2O5 to biomaterials (e.g., amino acid, protein, cells, virus, bacteria, ...). Thus, we are exploring the inactivation effects of N2O5 exposure on pathogen and virus, and modification of amino acid by the plasma-synthesized N2O5.Using the air APP device, we have investigated the inactivation effects on C. glo eosporioides (strawberry pathogen) and Qβ phage (RNA virus). 10μL of water droplet containing C. gloeosporioides was exposed to the plasma-synthesized N2O5 gas for 60 s, and typically 8h later, the germination rate of C. gloeosporioides conidium was evaluated as an indicator of inactivation effects. As a result, the N2O5 exposure significantly decreased the germination rate and the inactivation effect was not only due to pH decrease by HNO3aq transfer into the droplet from N2O5 gas. This indicates that N2O5aq, [NO2 +][ NO3 -]aq, or NO2 + aq may contribute to the inactivation. Also, mist particles containing Qβ phage were exposed to the plasma-synthesized N2O5gas, and the N2O5gas treatment resulted in over 3-log reduction in titer of Qβ phage. In addition, there were no significant difference of the inactivation effect between water and phosphate buffer mists, suggesting unique inactivation effects of N2O5gas other than pH decrease as noted above.Furthermore, we conducted experiments on the modification of amino acids such as tyrosine by plasma-synthesized N2O5gas. Tyrosine solution was treated by N2O5gas together with several reactive species such as O3gas or NO2gas, and it is found that dopachrome and nitrotyrosine were generated by the modification of tyrosine. Interestingly, dopachrome generation rate in N2O5gas with excess O3gas was most high, and the dopachrome generation was correlated with O3gas density. Further analysis using LC-PDA (liquid chromatography-photodiode array) and MS (mass spectrometer) quantified the tyrosine and tyrosine derivatives, and tyrosine was consumed at high rate, especially under N2O5gas with O3gas treatment.Major role of NO2 + aq is considered to be strong oxidizing capacity like OH radical, and N2O5gas triggers the generation of tyrosine intermediates. The tyrosine intermediates rapidly react with other reactive species such as O3gas and NO2gas, and then, dopachrome was significantly generated in N2O5gas with O3gas treatment and nitrotyrosine was in N2O5gas with NO2gas treatment.In the presentation, the details of the various biomaterial APP processes and plasma-synthesized N2O5 reaction pathway in the gas and liquid phase will be discussed.[1] Y. Kimura, K. Takashima, S. Sasaki, and T. Kaneko: J. Phys. D. Appl. Phys. 52, 064003 (2019).[2] K. Shimada, K. Takashima, Y. Kimura, K. Nihei, H. Konishi, and T. Kaneko: Plasma Process. Polym. 17, e1900004 (2020).[3] K. Takashima, Y. Hu, T. Goto, S. Sasaki, and T. Kaneko: J. Phys. D. Appl. Phys. 53, 354004 (2020).[4] K. Takashima, A.S. bin Ahmad Nor, S. Ando, H. Takahashi, and T. Kaneko: Jpn. J. Appl. Phys. 60, 010504 (2020).[5] S. Sasaki, K. Takashima, and T. Kaneko: Ind. Eng. Chem. Res. 60, 798 (2021).