Seike Musashi, Uda Makoto, Suzuki Toyoko, Minami Hideto, Higashimoto Shinya, Hirai Tomoyasu, Nakamura Yoshinobu, Fujii Syuji
Division of Applied Chemistry, Environmental and Biomedical Engineering, Graduate School of Engineering, Osaka Institute of Technology, 5-16-1 Omiya, Asahi-ku, Osaka 535-8585, Japan.
Department of Chemical Science and Engineering, Graduate School of Engineering, Kobe University, Rokko, Nada, Kobe 657-8501, Japan.
ACS Omega. 2022 Apr 8;7(15):13010-13021. doi: 10.1021/acsomega.2c00327. eCollection 2022 Apr 19.
Solvent-free chemical oxidative polymerizations of pyrrole and its derivatives, namely -methylpyrrole and -ethylpyrrole, were conducted by mechanical mixing of monomer and solid FeCl oxidant under nitrogen atmosphere. Polymerizations occurred at the surface of the oxidant, and optical and scanning electron microscopy studies confirmed production of atypical grains with diameters of a few tens of micrometers. Fourier transform infrared spectroscopy studies indicated the presence of hydroxy and carbonyl groups which were introduced during the polymerization due to overoxidation. The polymer grains were doped with chloride ions, and the chloride ion dopant could be removed by dedoping using an aqueous solution of sodium hydroxide, which was confirmed by elemental microanalysis and X-ray photoelectron spectroscopy studies. Water contact angle measurements confirmed that the larger the alkyl group on the nitrogen of pyrrole ring the higher the hydrophobicity and that the contact angles increased after dedoping in all cases. The grains before and after dedoping exhibited photothermal properties: the near-infrared laser irradiation induced a rapid temperature increase to greater than 430 °C. Furthermore, dedoped poly(-ethylpyrrole) grains adsorbed to the air-water interface and could work as an effective liquid marble stabilizer. The resulting liquid marble could move on a planar water surface due to near-infrared laser-induced Marangoni flow and could disintegrate by exposure to acid vapor via redoping of the poly(-ethylpyrrole) grains.
在氮气气氛下,通过单体与固体FeCl氧化剂的机械混合,进行了吡咯及其衍生物(即α-甲基吡咯和α-乙基吡咯)的无溶剂化学氧化聚合反应。聚合反应发生在氧化剂表面,光学显微镜和扫描电子显微镜研究证实生成了直径为几十微米的非典型颗粒。傅里叶变换红外光谱研究表明,聚合过程中由于过氧化引入了羟基和羰基。聚合物颗粒掺杂有氯离子,通过用氢氧化钠水溶液进行去掺杂可以去除氯离子掺杂剂,元素微量分析和X射线光电子能谱研究证实了这一点。水接触角测量证实,吡咯环氮上的烷基越大,疏水性越高,并且在所有情况下去掺杂后接触角都会增加。去掺杂前后的颗粒均表现出光热性能:近红外激光照射会使温度迅速升高至430℃以上。此外,去掺杂的聚(α-乙基吡咯)颗粒吸附在空气-水界面上,可以作为有效的液滴弹稳定剂。所得到的液滴弹由于近红外激光诱导的马兰戈尼流可以在平面水表面上移动,并且通过聚(α-乙基吡咯)颗粒的再掺杂暴露于酸蒸气中会解体。