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Synthesis and Surface-Active Properties of Trimeric-Type Anionic Surfactants Derived from Tris(2-aminoethyl)amine

机译:三(2-氨基乙基)胺衍生的三聚型阴离子表面活性剂的合成及表面活性

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Trimeric-type anionic surfactants (3C_n taAm,where n is a hydrocarbon chain length of 8,10,or 12) with three hydrocarbon chains and three carboxylate headgroups were synthesized from tris(2-aminoethyl)amine,and their properties were investigated by surface tension,electrical conductivity,dynami and static light-scattering,fluorescence of pyrene,and emulsification power techniques.The critical micelle concentrations (CMC) of 3C_ntaAm were 0.00092-0.00834 mmol dm~(-3),and the surface tensions at the CMC were 33.3-39.9 mN m~(-1).The areas per molecule occupied by 3C_10taAm and 3C_12taAm were extremely small,showing they were highly compact at the air/water interface.In addition,adsorption or micellization behavior of 3C_ntaAm waas estimated by parameters such as pC_20 (the efficiency of surface adsorption),CMC/C_20 (the ease of adsorption relative to the ease of micellization),and DELTAG_M~o (Gibbs energy of micellization).Dynamic and static light-scattering measurements of 3C_ntaAm showed a hydrodynamic radius of 45-621 nm above the CMC and aggregation numbers of 10-82 at the CMC,respectively.The fluorescence intensity ratio of the first to the third band in the emission spectra of pyrene started to lower from far above the CMC for 3C_8taAm and 3C_10taAm,and below the CMC for 3C_12taAm.This suggests that loose micelles or premicellar aggregates are formed in solutions.Mixture of aqueous solutions of 3C_ntaAm and toluene formed oil-in-water-type emulsions,and the stabilizing abilities were in the order of 3C_8taAm>3C_10taAm.The degee of emulsification of 3C_8taAm remained at 69% after 24h of standing.Thus,3C_ntaAm exhbited unique properties superior to monomeric or dimeric surfactants that were significantly inflenced by their hydrocarbon chain lengths.
机译:由三(2-氨基乙基)胺合成具有三个烃链和三个羧酸根基团的三聚型阴离子表面活性剂(3C_n taAm,n为8,10或12的烃链长度),并通过表面活性研究3C_ntaAm的临界胶束浓度(CMC)为0.00092-0.00834 mmol dm〜(-3),在CMC处的表面张力为33.3-39.9 mN m〜(-1)。3C_10taAm和3C_12taAm占据的每分子面积非常小,表明它们在空气/水界面处高度致密。此外,3C_ntaAm的吸附或胶束化行为还可以通过诸如如pC_20(表面吸附效率),CMC / C_20(相对于胶束化程度的吸附率)和DELTAG_M〜o(胶束化的吉布斯能量)。3C_ntaAm的动态和静态光散射测量结果hydro CMC上方45-621 nm的da流体力学半径和CMC处的聚集数分别为10-82。for的发射光谱中第一和第三波段的荧光强度比从远高于CMC开始降低。 3C_8taAm和3C_10taAm以及3C_12taAm的CMC下方。这表明溶液中形成了松散的胶束或胶束聚集体.3C_ntaAm的水溶液与甲苯的混合物形成了水包油型乳化液,其稳定能力按顺序排列静置24h后3C_8taAm的乳化度保持在69%。因此,3C_ntaAm具有独特的性能,优于其烃链长度显着影响的单体或二聚表面活性剂。

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