DOI QR코드

DOI QR Code

Synthesis and Properties of Anionic Sulfonate Surfactants Using Fatty Alcohol

Fatty alcohol을 이용한 음이온 술폰산계 계면활성제의 합성 및 물성

  • Cho, Jung-Eun (Dept. of Engineering Chemistry, Chungbuk National University) ;
  • Shin, Hye-Lin (Dept. of Engineering Chemistry, Chungbuk National University) ;
  • Jeong, Noh-Hee (Dept. of Engineering Chemistry, Chungbuk National University)
  • 조정은 (충북대학교 공과대학 공업화학과) ;
  • 신혜린 (충북대학교 공과대학 공업화학과) ;
  • 정노희 (충북대학교 공과대학 공업화학과)
  • Received : 2018.06.15
  • Accepted : 2018.09.28
  • Published : 2018.09.30

Abstract

In this study, surfactants were synthesized using fatty alcohols of 8, 10, 12 and 14 carbon chains length. The structures of the synthesized surfactants was confirmed by FT-IR and $^1H$-NMR analysis. The surface tension of the diluted surfactant was measured as 26~32 mN/m depending on the carbon length and the critical micelle concentration was measured as $10^{-3}{\sim}10^{-5}mol/L$.The minimum value per molecule of the synthesized sulfonic acid surfactant is 1.68 to $1.30nm^2$. The physical properties of the synthesized surfactants were determined by measuring the critical micelle concentration, foaming power, emulsifying stability, and contact angle.

본 연구에서는 지방 알코올을 이용하여 탄소 길이에 따른 술폰산계 음이온 계면활성제를 합성하였으며, 합성한 계면활성제들의 구조를 FT-IR과 $^1H$ NMR 분석을 통하여 확인하였다. 음이온 계면활성제의 임계미셀농도(critical micelle concentration: cmc)는 $10^{-5}{\sim}10^{-3}mol/L$이며, 임계미셀농도에서의 표면장력 값은 26~32 mN/m이었다. 합성한 술폰산계 계면활성제의 분자당 최소 영역값은 $1.68{\sim}1.30nm^2$이다. 음이온 계면활성제의 분자당 최소 영역이 감소하였다. 합성한 계면활성제의 물성은 임계 미셀농도, 기포력, 유화력, 접촉각을 측정하였다.

Keywords

References

  1. J.S. Park, J.C. Lim, "Inverstigation on a zwitterionic surfactant having ethylene oxide", Appl. Chem. Eng., Vol.10, No.2 pp. 605-608, (2006).
  2. N.H Jeong, S.S. Park, H.K. Jeong, K.H. Cho, K.D. Nam, "The synthesis of anionic oligomer surfactant with ${\alpha}$-sulfo alkanoic acid", J. of Korean Ind. & Eng. Chemistry., Vol.4, No.2 pp. 381-392 (1993).
  3. R. Yao, J. Qian, H. Li, A. Yasin, Y. Xieb, H. Yang, "Synthesis and high-performance of a new sarcosinate anionic surfactant with a long unsaturated tail". RSC Adv., Vol.4, pp. 2865-2872 (2014). https://doi.org/10.1039/C3RA44338H
  4. Y. Jin, S. Tian, J. Guo, X. Ren, X. Li , S. Gao . "Synthesis, characterization and exploratory application of anionic surfactant fatty acid methyl ester sulfonate from waste cooking oil". J Surfactants Deterg. Vol.19, pp. 467-475 (2016). https://doi.org/10.1007/s11743-016-1813-z
  5. Cserhati T, Forgacs E, Oros G. "Biological activity and environmental impact of anionic surfactants". Environment International. Vol.28, No.5 pp. 337-348 (2002). https://doi.org/10.1016/S0160-4120(02)00032-6
  6. S. Lee, B.J. Kim, J.G. Lee, J.C. Lim, "Synthesis and Characterization of Interfacal Properties of sorbitan Laurate surfactant", Appl. Chem. Eng., Vol.22, No.1 pp. 37-44 (2011).
  7. Matthew J. Scott, Malcolm N. Jones, "The biodegradation of surfactants in the environment", Biochimica et Biophysica Acta., Vol.1508, No.1 pp. 235-251 (2000). https://doi.org/10.1016/S0304-4157(00)00013-7
  8. D.H. Kim, S.K. Chang, S.W. Park, "Surfactants", J Anal Sci Technol., Vol.13, No.2 pp. 27-48 (2000).
  9. J.C. Lim, B.J. Kim, K.Y. Choi, "A study on synthesis of glycidol based nonionic surfactant", Korean Chem. Eng. Res., Vol.50, No.2 pp. 282-291 (2012). https://doi.org/10.9713/kcer.2012.50.2.282
  10. Geng T, Zhang C, Jiang Y, Ju H, Wang Y, "Synergistic effect of binary mixtures contained newly cationic surfactant: Interaction, aggregation behaviors and application properties", J. Mol. Liq., Vol.232, pp. 36-44 (2017). https://doi.org/10.1016/j.molliq.2017.02.055
  11. Rybinski W, Hill K, "Alkyl polyglycosides-properties and applications of a new class of surfactants". Angew Chem Int Ed., Vol.37, pp. 1328-1345 (1998). https://doi.org/10.1002/(SICI)1521-3773(19980605)37:10<1328::AID-ANIE1328>3.0.CO;2-9
  12. Raney KH, "Optimization of nonionic/anionic surfactant blends for enhanced oily soil removal". J Am Oil Chem Soc., Vol.68, No.7 pp. 525-531 (1991). https://doi.org/10.1007/BF02663829
  13. H.C. Kang, B.M. Lee, J.H. Yoon, M.J. Yoon, "Synthesis and surface-active properties of new photosensitive surfactants containing the azobenzene group". J Colloid Interface Sci., Vol.231, No.2 pp. 255-264 (2000). https://doi.org/10.1006/jcis.2000.7158
  14. M. Zhou, J. Zhao, X. Wang, J. Jing, L. Zhou, "Synthesis and characterization of novel surfactants 1,2,3-tri(2-oxypropylsulfonate-3-alkylether-propoxy) propanes". J Surfactants Deterg., Vol.16, pp. 665-672 (2013). https://doi.org/10.1007/s11743-013-1442-8
  15. M.M. El-Shahawi, A.A.S. Shalaby, A.M.E.D. Gabre, A.E.H.M. Ghonim, "Surface active properties and biological activities of novel anionic surfactant based on oxapyridazinone derivatives". J. Surfactants Deterg., Vol.19, pp. 137-144 (2016). https://doi.org/10.1007/s11743-015-1756-9
  16. KS M ISO 696, Surface active agents measurement of foaming power modified Ross-Miles method (2008).