Инд. авторы:	Urakaev F.K., Abuyeva B.B., Vorobyeva N.A., Mun G.A., Uralbekov B.M., Burkitbayev M.M.
Заглавие:	Sulfur nanoparticles stabilized in the presence of water-soluble polymers
Библ. ссылка:	Urakaev F.K., Abuyeva B.B., Vorobyeva N.A., Mun G.A., Uralbekov B.M., Burkitbayev M.M. Sulfur nanoparticles stabilized in the presence of water-soluble polymers // Mendeleev Communications. - 2018. - Vol.28. - Iss. 2. - P.161-163. - ISSN 0959-9436. - EISSN 1364-551X.
Внешние системы:	DOI: 10.1016/j.mencom.2018.03.017; РИНЦ: 35503121; SCOPUS: 2-s2.0-85044777425; WoS: 000435626800017;
Реферат:	eng: A method was developed to prepare sulfur nanoparticles (nanosulfur) via reaction between sodium thiosulfate and sulfuric acid in the presence of water-soluble poly-N-vinylpyrrolidone (PVP) with different molecular weights. Polymeric hydrogel ointments were prepared from agar-agar, PVP, poly(ethylene glycol) solutions with virable concentrations of sodium thiosulfate and sulfuric acid. The ointment samples showed antibacterial and antifungal activities against Staphylococcus aureus, Escherichia coli and Candida guilliermondii. © 2018
Ключевые слова:	REDUCTION; NUCLEATION; CATHODE; NITROGEN; COMPOSITE; BATTERIES; HIGH-PERFORMANCE; DOPED POROUS CARBON; MECHANISM; PARTICLES;
Издано:	2018
Физ. характеристика:	с.161-163
Цитирование:	1. Kutney, G., Sulfur: History, Technology Applications and Industry. 2013, ChemTec Publishing, Toronto. 2. Kumar, R., Nair, K.K., Alam, M.I., Gogoi, R., Singh, P.K., Srivastava, C., Yadav, S., Gopal, M., Choudhury, S.R., Pradhan, S., Goswami, A., Curr. Sci. India, 100, 2011, 1542. 3. F. Kh. Urakaev, A.I. Bulavchenko, B.M. Uralbekov, I.A. Massalimov, B.B. Tatykaev, A.K. Bolatov, D.N. Zharlykasimova and M. M. Burkitbayev, Colloid J., 2016, 78, 210 (Kolloid. Zh., 2016, 78, 193). 4. Suleiman, M., Al-Masri, M., Ali, A.A., Aref, D., Hussein, A., Saadeddin, I., Warad, I., J. Mater. Environ. Sci., 6, 2015, 513. 5. Choudhury, S.R., Mandal, A., Ghosh, M., Basu, S., Chakravorty, D., Goswami, A., Appl. Microbiol. Biotechnol., 97, 2013, 5965. 6. Rao, K.J., Paria, S., RSC Adv., 3, 2013, 10471. 7. Massalimov, I.A., Medvedev, Yu.A., Urakaev, F.Kh., Ahmed, I.S.A., Burkitbayev, M.M., Uralbekov, B.M., Am. Eurasian J. Agric. Environ. Sci., 16, 2016, 652. 8. Massalimov, I.A., Yanakhmetov, M.R., Chuykin, A.E., Mustafin, A.G., Study Civil Eng. Architecture, 2, 2013, 19. 9. Chen, T., Cheng, B., Zhu, G., Chen, R., Hu, Y., Ma, L., Lv, H., Wang, Y., Liang, J., Tie, Z., Jin, Z., Liu, J., Nano Lett., 17, 2017, 437. 10. Jeong, T.-G., Chun, J., Cho, B.-W., Lee, J., Kim, Y.-T., Sci. Rep., 7, 2017, 42238. 11. Li, F., Liu, W., Lai, Y., Qin, F., Zou, L., Zhang, K., Li, J., J. Alloys Compd., 695, 2017, 1743. 12. Li, J., Guo, J., Deng, J., Huang, Y., Mater. Lett., 189, 2017, 188. 13. Nie, L., Wang, H., Ma, J., Liu, S., Yuan, R., J. Mater. Sci., 52, 2017, 3566. 14. Shao, D., Smolianova, I., Tang, D., Zhang, L., RSC Adv., 7, 2017, 2407. 15. Wang, H., Huang, K., Wang, P., Zhong, J., J. Alloys Compd., 691, 2017, 613. 16. Zhang, Y., Li, K., Huang, J., Wang, Y., Peng, Y., Li, H., Wang, J., Zhao, J., Carbon, 114, 2017, 8. 17. Lan, Y., Deng, B., Kim, C., Thornton, E.C., Xu, H., Environ. Sci. Technol., 39, 2005, 2087. 18. Cai, A., Wang, X., Qi, Y., Ma, Z., Appl. Surf. Sci., 2017, 391 part B, 484. 19. Khang, N.C., Van, D.Q., Thuy, N.M., Minh, N.V., Minh, P.N., J. Phys. Chem. Solids, 99, 2016, 119. 20. Qian, H., Tang, J., Wang, Z., Kim, J., Kim, J.H., Alshehri, S.M., Yanmaz, E., Wang, X., Yamauchi, Y., Chem. Eur. J., 22, 2016, 18259. 21. Sahoo, M., Ramaprabhu, S., Energy, 119, 2017, 1075. 22. Zhang, K., Li, J., Liu, W., Liu, J., Yan, C., Int. J. Hydrogen Energy, 41, 2016, 22643. 23. Ghanemi, K., Nikpour, Y., Omidvar, O., Maryamabadi, A., Talanta, 85, 2011, 763. 24. E. Bura-Nakić, M. Marguš, D. Jurašin, I. Milanović and I. Cigleneč=ki-Jušić, Geochem. Trans., 2015, 16, 1, DOI: 10.1186/s12932-015-0016-2. 25. Li, R., Yang, T., Li, Z., Gu, Z., Wang, G., Liu, J., Anal. Chim. Acta, 954, 2017, 43. 26. Urakaev, F.Kh., Mendeleev Commun., 2005, 106. 27. Urakaev, F.Kh., Combust. Sci. Technol., 185, 2013, 1281. 28. La Mer, V.K., Ind. Eng. Chem., 44, 1952, 1270. 29. Urakaev, F.Kh., Bazarov, L.Sh., Meshcheryakov, I.N., Feklistov, V.V., Drebushchak, T.N., Savintsev, Yu.P., Gordeeva, V.I., Shevchenko, V.S., J. Cryst. Growth, 205, 1999, 223. 30. Urakaev, F.Kh., Drebushchak, T.N., Savintsev, Yu.P., Drebushchak, V.A., Mendeleev Commun., 2003, 37. 31. Urakaev, F.Kh., Int. J. Comput. Mater. Sci. Surf. Eng., 4, 2011, 69. 32. Buhler, V., Polyvinylpyrrolidone: Excipients for Pharmaceuticals (Povidone, Crosspovidone and Copovidone). 2005, Springer, Berlin. 33. B. V. Robinson, F.M. Sullivan, J.F. Borzelleca and S. L. Schwartz, PVP: A Critical Review of the Kinetics and Toxicology of Polyvinylpyrrolidone (Povidone), Lewis Publisher, Chelsea, MI, 1990. 34. Poly(Ethylene Glycol) Chemistry. Biotechnical and Biomedical Applications, ed. J. M. Harris, Springer, Boston, MA, 1992. 35. Xie, X.-Y., Li, L.-Y., Zheng, P.-S., Zheng, W.-J., Bai, Y., Cheng, T.-F., Liu, J., Mater. Res. Bull., 47, 2012, 3665. 36. Sepassi, S., Goodwin, D.J., Drake, A.F., Holland, S., Leonard, G., Martini, L., Lawrence, M.J., J. Pharm. Sci., 96, 2007, 2655. 37. Shmatko, N.Yu., Sanina, N.A., Anokhin, D.V., Piryazev, A.A., Ivanov, D.A., Kulikov, A.V., Aldoshin, S.M., (eds.) Russ. Chem. Bull., Int., 2015, 1616 64 (Izv. Akad. Nauk, Ser. Khim., 2015 1616). 38. Rac, O., Suchorska-Woźniak, P., Fiedot, M., Teterycz, H., Beilstein J. Nanotechnol., 5, 2014, 2192. 39. Kurmaz, S.V., Obraztsova, N.A., Mendeleev Commun., 25, 2015, 350. 40. Shah, S., Noor, I.M., Pitawala, J., Albinson, I., Bandara, T.M.W.J., Mellander, B.-E., Arof, A.K., Opt. Mater. Express, 7, 2017, 2069. 41. Torchilin, V.D., Winslow, R., Vandegriff, K.D., Intaglietta, M., (eds.) Advances in Blood Substitutes: Industrial Opportunities and Medical Challenges, 2012, Springer Science & Business Media, 251–297 ch. 13. 42. J. Rosiak, A. Rucinska-Rybus and W. Pekala, Patent US 4871490 A, 1989.