Faculty of Chemical Engineering and Light Industry , Guangdong University of Technology , Guangzhou , Guangdong 510006 , China.
Institute of Bioengineering and Nanotechnology , 31 Biopolis Way, The Nanos , 138669 , Singapore.
Langmuir. 2018 Jul 10;34(27):8058-8064. doi: 10.1021/acs.langmuir.8b01643. Epub 2018 Jun 27.
Use of carrier solvents to assist dissolution of phase-selective organogelators (PSOGs) before application in oil gelation is a common approach for solution-based gelators. Because of the competition in H-bonds by the polar carrier solvent, decreased gelling ability of PSOGs was often observed. That is, while data are available, the previously documented biphasic minimum gelling concentrations (BMGCs) are much larger than the MGCs determined using heating-cooling cycle for the same PSOG against the same oil. In this study, we show that, by minimizing amount of polar carrier solvent used, the gelling ability of PSOGs actually can be enhanced very substantially, rather than being weakened. More specifically, we demonstrate that use of a minute amount of polar carrier solvents of different types (e.g., ethyl acetate, acetone, acetonitrile, and tetrahydrofuran) significantly enhances the gelling ability of seven structurally different organogelators in hydrophobic oil. In particular, with the use of 5 vol % essentially nontoxic ethyl acetate, application of this previously unexplored strategy onto four monopeptide-based PSOGs produces up to 11-fold improvement in biphasic gelling ability toward seven (un)weathered crude oils of widely ranging viscosities. While collectively overcoming many problematic issues (slow gelling action, low gelling ability, or a need to use hot or toxic solvent for dissolution of gelator) associated with PSOGs, this surprisingly simple yet powerful and reliable method produces unprecedented rapid supergelation of crude oil at room temperature, with BMGCs of as low as 0.38 w/v % (e.g., 3.8 g per liter of crude oil) and an averaged reduction in material cost of gelators by 85-97%.
在将选择性相凝胶剂(PSOG)应用于油凝胶化之前,使用载体溶剂来辅助其溶解是基于溶液的凝胶剂的常用方法。由于极性载体溶剂竞争氢键,PSOG 的凝胶能力通常会降低。也就是说,虽然有数据可用,但以前记录的两相最小凝胶浓度(BMGC)比使用相同 PSOG 针对相同油进行加热-冷却循环确定的 MGC 大得多。在这项研究中,我们表明,通过最小化使用的极性载体溶剂的量,PSOG 的凝胶能力实际上可以得到很大的增强,而不是减弱。更具体地说,我们证明了使用不同类型的极少量极性载体溶剂(例如乙酸乙酯、丙酮、乙腈和四氢呋喃)可以显著增强七种结构不同的有机凝胶剂在疏油中的凝胶能力。特别是,使用 5 体积%的基本上无毒的乙酸乙酯,将这种以前未探索的策略应用于四种基于单肽的 PSOG 上,可使七种(未)风化原油的两相凝胶能力提高 11 倍,这些原油的粘度范围很广。虽然这种方法共同克服了与 PSOG 相关的许多问题(凝胶作用缓慢、凝胶能力低,或需要使用热或有毒溶剂来溶解凝胶剂),但这种简单而强大且可靠的方法却能在室温下产生前所未有的快速稠化原油的效果,其 BMGC 低至 0.38 w/v%(例如,每升原油 3.8 克),凝胶剂的材料成本平均降低 85-97%。