Wang Sijia, Wu Ning
Department of Chemical & Biological Engineering, Colorado School of Mines , 1500 Illinois Street, Golden, Colorado 80401, United States.
ACS Appl Mater Interfaces. 2014 Nov 26;6(22):20164-70. doi: 10.1021/am505745v. Epub 2014 Oct 30.
Colloidal particles have been used extensively for stabilizing oil-water interfaces in petroleum, food, and cosmetics industries. They have also demonstrated promising potential in the encapsulation and delivery of drugs. Our work is motivated by challenging applications that require protecting and transporting active agents across the water-oil interfaces, such as delivering catalysts to underground oil phase through water flooding for in situ cracking of crude oil. In this Research Article, we successfully design, synthesize, and test a unique type of bicompartmental targeting vehicle that encapsulates catalytic molecules, finds and accumulates at oil-water interface, releases the catalysts toward the oil phase, and performs hydrogenation reaction of unsaturated oil. This vehicle is based on colloidal dimers that possess structural anisotropy between two compartments. We encapsulate active species, such as fluorescent dye and catalytic molecules in one lobe which consists of un-cross-linked polymers, while the other polymeric lobe is highly cross-linked. Although dimers are dispersible in water initially, the un-cross-linked lobe swells significantly upon contact with a trace amount of oil in aqueous phase. The dimers then become amphiphilic, migrate toward, and accumulate at the oil-water interface. As the un-cross-linked lobe swells and eventually dissolves in oil, the encapsulated catalysts are fully released. We also show that hydrogenation of unsaturated oil can be performed subsequently with high conversion efficiency. By further creating the interfacial anisotropy on the dimers, we can reduce the catalyst release time from hundred hours to 30 min. Our work demonstrates a new concept in making colloidal emulsifiers and phase-transfer vehicles that are important for encapsulation and sequential release of small molecules across two different phases.
胶体颗粒已被广泛应用于石油、食品和化妆品行业中油水界面的稳定。它们在药物的封装和递送方面也显示出了巨大的潜力。我们的工作受到具有挑战性的应用的推动,这些应用需要在油水界面上保护和运输活性剂,例如通过注水将催化剂输送到地下油相中以实现原油的原位裂解。在这篇研究文章中,我们成功设计、合成并测试了一种独特的双隔室靶向载体,该载体封装催化分子,在油水界面处发现并聚集,向油相释放催化剂,并进行不饱和油的氢化反应。这种载体基于胶体二聚体,两个隔室之间具有结构各向异性。我们将活性物质,如荧光染料和催化分子封装在由未交联聚合物组成的一个叶瓣中,而另一个聚合物叶瓣则高度交联。虽然二聚体最初可分散在水中,但未交联的叶瓣在与水相中微量的油接触时会显著膨胀。然后二聚体变得具有两亲性,向油水界面迁移并聚集。随着未交联的叶瓣膨胀并最终溶解在油中,封装的催化剂被完全释放。我们还表明,随后可以以高转化效率进行不饱和油的氢化反应。通过进一步在二聚体上产生界面各向异性,我们可以将催化剂的释放时间从数百小时缩短至30分钟。我们的工作展示了一种制造胶体乳化剂和相转移载体的新概念,这对于小分子在两个不同相之间的封装和顺序释放非常重要。