研究论文

两个非离子表面活性剂复配体系的NMR研究

  • 赵瑞格 ,
  • 张卫红 ,
  • 马二倩 ,
  • 于海涛 ,
  • 杨秋青
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  • 1. 河北师范大学 化学与材料科学学院, 河北 石家庄 050024;
    2. 河北师范大学 分析测试中心, 河北 石家庄 050024

收稿日期: 2017-06-20

  网络出版日期: 2018-03-05

基金资助

河北省高等学校科学技术资助项目(ZD2015030);河北省自然科学基金资助项目(B2016205249).

An NMR Study on Two Mixed Micelles Formed by Nonionic Surfactants

  • ZHAO Rui-ge ,
  • ZHANG Wei-hong ,
  • MA Er-qian ,
  • YU Hai-tao ,
  • YANG Qiu-qing
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  • 1. College of Chemistry and Material Science, Hebei Normal University, Shijiazhuang 050024, China;
    2. Analysis and Testing Center, Hebei Normal University, Shijiazhuang 050024, China

Received date: 2017-06-20

  Online published: 2018-03-05

摘要

通过核磁共振(NMR)技术对NP-10/Tween40和NP-10/C10E6两个复配体系在不同比例下混合胶束的排列方式、相互作用点及其不同分子间与相同分子间的作用变化进行了研究和比较.二维NOESY实验结果证明了:(1)这两种复配体系的相互作用是随混合比例的不同而变化的;(2)两个复配体系的不同分子间相互作用点有相同之处,但NP-10/Tween40分子间相互作用大于NP-10/C10E6.横向弛豫时间(T2)表明,当NP-10/Tween40和NP-10/C10E6体系的混合比分别为1:2和1:4后,其不同分子间的相互作用开始减小,相同分子间作用开始起主导作用,暗示了复配体系中的理想混合配比和协同效应的变化.横向弛豫时间与纵向弛豫时间之比(TR=T2/T1)反映了与NP-10/C10E6相比,NP-10/Tween40混合胶束分子链的运动受限更加严重.空间距离计算结果也佐证了NP-10/Tween40和NP-10/C10E6复配体系的较为理想的配比分别为1:2和1:4;NP-10/Tween40不同分子间距离小于NP-10/C10E6.

本文引用格式

赵瑞格 , 张卫红 , 马二倩 , 于海涛 , 杨秋青 . 两个非离子表面活性剂复配体系的NMR研究[J]. 波谱学杂志, 2018 , 35(1) : 81 -89 . DOI: 10.11938/cjmr20172587

Abstract

NMR techniques were used to study the relative arrangement and interaction sites in mixed micelles formed in NP-10/Tween40 and NP-10/C10E6 aqueous solutions. The results of two-dimensional NOESY experiments and relaxation time measurements showed that the interaction site of these two pairs of mixed surfactants were similar, but the intermolecular interaction between NP-10 and Tween40 was stronger than that between NP-10 and C10E6. T2 measurements demonstrated that inter-heteromolecular interactions decreased when the molar concentrations of Tween40 and C10E6 were larger than 2 and 4 folds of that of NP-10, respectively. Under such circumstances, the inter-homomolecular interactions began to play a key role, indicative of the ideal mixture molar ratio and the change of synergistic effect in the complex systems. T2/T1 ratio measurements indicated that molecular chain movement in the NP-10/Tween40 mixture was more limited than that in the NP-10/C10E6 mixture. The above conclusions were verified by spatial distance measurements.

参考文献

[1] YANG Q Q, ZHOU Q, SOMASUNDARAN P. Mixed micelles of octane-1,8 bis(dodecyl dimethyl ammonium chloride) and n-dodecyl-β-maltoside by <sup>1</sup>H NMR study[J]. Colloids and Surfaces A, 2007, 305(1-3):22-28.[2] YANG Q Q, ZHOU Q, SOMASUNDARAN P. NMR study of micellar microstructures of cationic single-chain and Gemini surfactants and their mixtures with nonionic surfactant n-dodecyl-β-maltoside[J]. Colloids and Surfaces A, 2008, 322(1-3):40-46.[3] YANG Q Q, ZHOU Q, SOMASUNDARAN P. <sup>1</sup>H NMR study of micelles formed by mixture of nonionic n-dodecyl-β-D-maltoside and cationic geminisurfactants[J]. J Mol Liq, 2009, 146(3):105-111.[4] MA E Q, LI Y X, ZHAO R G, et al. Interactions between NP-10 and single/double chain quaternary ammonium salts studied by NMR spectroscopy[J]. Chinese J Magn Reson, 2017, 34(1):16-24. 马二倩, 李永肖, 赵瑞格, 等. NP-10与单链、双链季铵盐三种复配体系相互作用规律的NMR研究[J]. 波谱学杂志, 2017, 34(1):16-24.[5] LIN J H, CHEN W S, HOU S S. NMR studies on effects of tetraalkyl ammonium bromides on micellization of sodium dodecylsulfate[J]. J Phys Chem B, 2013, 117(40):12076-12085.[6] PODO F, RAY A, NEMETHY G. Structure and hydration of nonionic detergent micelles. high resolution nuclear magnetic resonance study[J]. J Am Chem Soc, 1973, 95(19):6164-6171.[7] YUAN H Z, DU Y R, ZHAO S, et al. Self-aggregation of surfactants in water solution by NMR[J]. Sci China Ser A, 1999, 42(3):319-324.[8] GAO H C, FANG X W, MAO S Z, et al. Conformation and dynamics of polyoxyethylene lauryl ether(Brij-35) chains in aqueous micellar solution studied by 2D NOESY and <sup>1</sup>H NMR relaxation[J]. Sci China Ser B, 2002, 45(2):143-150.[9] BLOKHIN D S, FAYZULLINA A R, FILIPPOV A V, et al. Spatial structure of fibrinopeptide B in water solution with DPC micelles by NMR spectroscopy[J]. J Mol Struct, 2015, 1102:91-94.
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