Abstract
A hollow spherical highly hydrophilic polyaniline sulfonic acid catalyst has been successfully prepared by emulsion polymerization and SO3 liquid sulfonation using modified polystyrene microspheres (PS) as a template. Acid value of the solid acid catalyst is 2.516 mmol/g. Morphology, structure and thermal stability of the catalyst have been studied by XRD, SEM, TEM, FT-IR, X-ray photoelectron spectroscopy (XPS), and TGA. It has been proven that doping and sulfonation of PANI and SO3 lead to new molecule that retains the PANI matrix material. In view of close structure-activity relationship, it has been applied to the efficient synthesis of bis(indolyl)methanes (BIMs) in water-ethanol phase.
Similar content being viewed by others
REFERENCES
Oueiny, C., Berlioz, S., and Perrin, F.X., Prog. Polym. Sci., 2014, vol. 39, p. 707. https://doi.org/10.1016/j.progpolymsci.2013.08.009
Wang, H., Lin, J., and Shen, Z.X., J. Sci. Adv. Mater. Devic., 2016, vol. 1, p. 225. https://doi.org/10.1016/j.jsamd.2016.08.001
Shen, Y.F., Yuan, D.D., Ai, X.P., Yang, H.X., and Zhou, M., Electrochem. Commun., 2014, vol. 49, p. 5. https://doi.org/10.1016/j.elecom.2014.09.016
Geethalakshmi, D., Muthukumarasamy, N., and Balasundaraprabhu, R., Mat. Sci. Semicon. Proc., 2016, vol. 51, p. 71. https://doi.org/10.1016/j.mssp.2016.05.006
Lashkenari, M.S., Davodi, B., Ghorbani, M., and Eisazadeh, H., High. Perform. Polym., 2012, vol. 24, p. 345. https://doi.org/10.1177/0954008311436222
Drelinkiewicz, A., Kalemba-Jaje, Z., Lalik, E., and Kosydar, R., Fuel., 2014, vol. 116, p. 760. https://doi.org/10.1016/j.fuel.2013.08.079
Palaniappan, S. and Ram, M.S., Green. Chem., 2002, vol. 4, p. 53. https://doi.org/10.1039/b109891h
Zięba, A., Drelinkiewicz, A., Konyushenko, E.N., and Stejskal, J., Appl. Catal. A: Gen., 2010, vol. 383, p. 169. https://doi.org/10.1016/j.apcata.2010.05.042
Zięba, A., Drelinkiewicz, A., Chmielarz, P., Matachowski, L., and Stejskal, J., Appl. Catal. A: Gen., 2010, vol. 387, p. 13. https://doi.org/10.1016/j.apcata.2010.07.060
Drelinkiewicz, A., Kalemba-Jaje, Z., Lalik, E., Zięba, A., Mucha, D., Konyushenko, E.N., and Stejskal, J., Appl. Catal. A: Gen., 2013, vol. 455, p. 92. https://doi.org/10.1016/j.apcata.2013.01.022
Zheng, Y., Zheng, Y., Yang, S., Guo, Z., Zhang, T., Song, H., and Shao, Q., Green. Chem. Lett. Rev., 2017, vol. 10, p. 202. https://doi.org/10.1080/17518253.2017.1342001
Ravi, K., Krishnakumar, B., and Swaminathan, M., Synth. React. Inoge. M., 2015, vol. 45, p. 1380. https://doi.org/10.1080/15533174.2013.862710
Shirini, F., Fallah-Shojaei, A., Samavi, L., and Abedini, M., RSC. Adv., 2016, vol. 6, p. 48469. https://doi.org/10.1039/C6RA04893E
Shirini, F. and Lati, M.P., J. Iran. Chem. Soc., 2017, vol. 14, p. 75. https://doi.org/10.1007/s13738-016-0959-y
Feng, X., Mao, C., Yang, G., Hou, W., and Zhu, J.J., Langmuir., 2006, vol. 22, p. 4384. https://doi.org/10.1021/la053403r
Ma, G., Wen, Z., Jin, J., Lu, Y., Wu, X., Wu, M., and Chen, C., J. Mater. Chem. A, 2014, vol. 2, p. 10350. https://doi.org/10.1039/C4TA00483C
Kang, E.T., Neoh, K.G., and Tan, K.L., Prog. Polym. Sci., 1998, vol. 23, p. 277. https://doi.org/10.1016/S0079-6700(97)00030-0
Kim, S.G., Kim, J.W., Choi, H.J., Suh, M.S., Shin, M.J., and Jhon, M.S., Colloid. Polym. Sci., 2000, vol. 278, p. 894. https://doi.org/10.1007/s003960000360
Zhu, Y., Hu, D., Wan, M.X., Jiang, L., and Wei, Y., Adv. Mater., 2007, vol. 19, p. 2092. https://doi.org/10.1002/adma.200602135
Trchova, M., Stejskal, J., and Prokeš, J., Synthetic. Met., 1999, vol. 101, p. 840. https://doi.org/10.1016/S0379-6779(98)01310-1
Pouget, J.P., Jozefowicz, M.E., Epstein, A.E.A., Tang, X., and MacDiarmid, A.G., Macromolecules, 1991, vol. 24, p. 779. https://doi.org/10.1021/ma00003a022
Łużny, W., Śniechowski, M., and Laska, J., Synthetic. Met., 2002, vol. 126, p. 27. https://doi.org/10.1016/S0379-6779(01)00477-5
Murugesan, R. and Subramanian, E., Mater. Chem. Phys., 2003, vol. 80, p. 731. https://doi.org/10.1016/S0254-0584(03)00127-5
Tan, K.L., Tan, B.T.G., Kang, E.T., and Neoh, K.G., Phys. Rev. B, 1989, vol. 39, p. 8070. https://doi.org/10.1103/PhysRevB.39.8070
Liu, M.J., Tzou, K., and Gregory, R.V., Synthetic. Met., 1994, vol. 63, p. 67. https://doi.org/10.1016/03796779(94)90251-8
Shishkanova, T.V., Sapurina, I., Stejskal, J., Král, V., and Volf, R., Anal. Chim. Acta, 2005, vol. 553, p. 160. https://doi.org/10.1016/j.aca.2005.08.018
Blinova, N.V., Stejskal, J., Trchová, M., and Prokeš, J., Polym. Int., 2008, vol. 57, p. 66. https://doi.org/10.1002/pi.2312
Funding
This work was financially supported by the Major Innovation Projects for Building First-class Universities in China’s Western Region (no. ZKZD 2017003), the National First-rate Discipline Construction Project of Ningxia (no. NXYLXK2017A04) and the National Natural Science Foundation of China (no. 21862013).
Author information
Authors and Affiliations
Corresponding author
Ethics declarations
No conflict of interest was declared by the authors.
Rights and permissions
About this article
Cite this article
Wu, Z., Wang, G., Yuan, S. et al. Synthesis, Characterization, and Properties of Highly Hydrophilic Polyaniline Sulfonic Acid. Russ J Gen Chem 90, 1055–1061 (2020). https://doi.org/10.1134/S1070363220060195
Received:
Revised:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1134/S1070363220060195