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Individual and mixed adsorption of alkylcarboxylbetaines and fatty amide ethoxylates at Daqing sandstone/water interface

机译:大庆砂岩/水界面的烷基羧基甜菜碱和脂肪酰胺乙氧基化物的单独吸附和混合吸附

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The individual adsorption of a series of alkylcarboxylbetaines, including single long-alkyl dimethylcarboxylbetaine (C _(12)B, C _(14)B, C _(16)B, and C _(18)B) and didodecylmethyl-carboxylbetaine (diC _(12)B), as well as fatty amide ethoxylates (C _(12)MEA-EO _1 and CMEA-EO _2), at negatively charged Daqing sandstone/water interface at 45°C were studied and compared with that of typical anionic and cationic surfactants. The results show that the saturated adsorption of surfactants at solid/water interface can be well characterized by a layer number, n, defined as the ratio of the saturated adsorption at solid/water interface to that at air/water interface, and in general the saturated adsorption of different species follows an order of anionic (n<0.5)1)2). The adsorption of the alkylcarboxylbetaines is initially driven by the electrostatic interaction between the positive charges in surfactant molecules and negative charges on surface followed by the chain-chain interaction which inducing admicelle formation on the solid surface. The single long-alkyl carboxylbetaines have similar saturated adsorption, i.e. with n between 1.49 and 1.71, but the double long-alkyl carboxylbetaine, diC _(12)B, gives a relatively lower n value (1.07) although it has a comparative saturated adsorption at solid/water interface due to its high adsorption at air/water interface. Lacking of the electrostatic interaction, the saturated adsorption of the fatty amide ethoxylates is in general low, as indicated by their low n values (0.595 and 0.526).For mixed adsorption systems nearly ideal mixing and middle synergism are observed for diC _(12)B/C _(12)B (homologous mixture), and diC _(12)B/C _(12)MEA-EO _1/(zwitterioniconionic) mixtures, but strong synergisms are observed for SDS/C _(12)B and SDS/C _(16)B (anionic/zwitterionic) mixtures. Thus for surfactant-polymer flooding the achievement of low adsorption retention depends strongly on the species selected if mixed surfactants are necessary.
机译:一系列烷基羧基甜菜碱的单独吸附,包括单个长烷基二甲基羧基甜菜碱(C _(12)B,C _(14)B,C _(16)B和C _(18)B)和双十二烷基甲基羧基甜菜碱(研究了在45°C带负电荷的大庆砂岩/水界面处的diC _(12)B)以及脂肪酰胺乙氧基化物(C _(12)MEA-EO _1和CMEA-EO _2)并将其与典型的阴离子和阳离子表面活性剂。结果表明,表面活性剂在固/水界面处的饱和吸附可以很好地表征为层数n,n定义为固/水界面处的饱和吸附与空气/水界面处的饱和吸附之比,通常不同物种的饱和吸附遵循阴离子(n <0.5)<非离子(0.5 1)<阳离子表面活性剂(n> 2)的顺序。烷基羧基甜菜碱的吸附最初是由表面活性剂分子中的正电荷与表面上的负电荷之间的静电相互作用驱动的,然后是链-链相互作用,后者诱导了固体表面上的胶束形成。单个长烷基羧基甜菜碱具有相似的饱和吸附,即n在1.49和1.71之间,但双长烷基羧基甜菜碱diC _(12)B尽管具有相对的饱和吸附,但其n值较低(1.07)。由于其在空气/水界面处的高吸附性,因此在固体/水界面处具有吸附性。缺乏静电相互作用,脂肪酰胺乙氧基化物的饱和吸附通常较低,如n值较低(0.595和0.526)所示。对于混合吸附系统,diC _(12)观察到接近理想的混合和中等协同作用B / C _(12)B(同源混合物)和diC _(12)B / C _(12)MEA-EO _1 /(两性离子/非离子)混合物,但在SDS / C _(12 B和SDS / C _(16)B(阴离子/两性离子)混合物。因此,对于表面活性剂-聚合物驱来说,如果需要混合表面活性剂,则低吸附保持力的实现很大程度上取决于所选择的种类。

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