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Creating long-range hydrophobic forces by coadsorption of ionic and neutral surfactants.

机译:通过离子表面活性剂和中性表面活性剂的共同吸附产生长程疏水力。

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摘要

A Mark IV surface force apparatus was used to measure surface forces between mica surfaces in dodecylamine hydrogen chloride (DAHCl) solutions at pH 5.7 in the presence and absence of long-chain alcohols. With DAHCl alone, only "short-range" hydrophobic forces were observed with decay lengths of 1.2-1.4 nm. In the presence of octanol, long range hydrophobic forces were observed with decay lengths in the range of 2.0-6.8 nm. In the presence of dodecanol, the decay length became as large as 9.0 nm, which represents the strongest ever recorded hydrophobic force with soluble single-chain surfactants. The appearance of the long-range hydrophobic forces in the presence of neutral surfactants can be attributed to the coadsorption mechanism, in which neutral surfactant molecules adsorb along with dodecylammonium (DAH;Long-range hydrophobic forces were also measured between mica surfaces in DAHCl solutions at pH 9.5, at which considerable amount of neutral amine (DA) is produced as a result of hydrolysis. The force measurements exhibit long-range hydrophobic forces with decay length of 5.5 nm. Appearance of the long-range hydrophobic force at this pH can be attributed to the coadsorption of DA and DAH;The force measurements conducted at 10.1 show that phase-separated amine is formed on the mica surface at a 50-times lower concentration than for the bulk precipitation. Above this concentration, the mica surfaces do not jump into contact with each other, suggesting that the phase-separated amine renders the surface hydrophilic. Furthermore, the force measurements conducted at pH 10.1 show repulsive steric forces, which become stronger with increasing DAHCl concentration. The adhesion force between mica surfaces becomes zero when surface precipitation occurs, while water contact angle is less sensitive.;Hydrophobic force increases sharply when advancing water contact angle (
机译:在存在和不存在长链醇的情况下,使用Mark IV表面力仪器测量pH值为5.7的十二烷基胺氯化氢(DAHCl)溶液中云母表面之间的表面力。单独使用DAHCl时,仅观察到“短程”疏水力,衰减长度为1.2-1.4 nm。在存在辛醇的情况下,观察到了长范围的疏水力,其衰变长度为2.0-6.8 nm。在十二烷醇的存在下,衰变长度变得最大为9.0 nm,这代表有记录的可溶性单链表面活性剂最强的疏水力。在存在中性表面活性剂的情况下出现长程疏水力可归因于共吸附机理,其中中性表面活性剂分子与十二烷基铵盐(DAH)一起吸附;还测量了DAHCl溶液中云母表面之间的长程疏水力。 pH值为9.5,在此条件下水解会产生大量的中性胺(DA)。测得的力表现为衰变长度为5.5 nm的长距离疏水力,在此pH值下长距离疏水力的外观为归因于DA和DAH的共吸附;在10.1上进行的力测量表明,在云母表面上形成的相分离胺的浓度比整体沉淀低50倍,在该浓度以上,云母表面不会跳动。相互接触,表明相分离的胺使表面具有亲水性,此外,在pH 10.1下进行的力测量显示排斥空间力,随着DAHCl浓度的增加而增强。当发生表面沉淀时,云母表面之间的附着力变为零,而水接触角则较不敏感;当水接触角增大时,疏水力急剧增加(

著录项

  • 作者

    Ravishankar, S. A.;

  • 作者单位

    Virginia Polytechnic Institute and State University.;

  • 授予单位 Virginia Polytechnic Institute and State University.;
  • 学科 Materials science.
  • 学位 Ph.D.
  • 年度 1995
  • 页码 190 p.
  • 总页数 190
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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