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Fatty alcohol을 이용한 음이온 술폰산계 계면활성제의 합성 및 물성

Synthesis and Properties of Anionic Sulfonate Surfactants Using Fatty Alcohol

  • 조정은 (충북대학교 공과대학 공업화학과) ;
  • 신혜린 (충북대학교 공과대학 공업화학과) ;
  • 정노희 (충북대학교 공과대학 공업화학과)
  • 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)
  • 투고 : 2018.06.15
  • 심사 : 2018.09.28
  • 발행 : 2018.09.30

초록

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.

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.

키워드

참고문헌

  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).