Department of Biology, Norwegian University of Science and Technology, NO-7491, 7491, Trondheim, Norway.
SINTEF Ocean, NO-7465, 7465, Trondheim, Norway.
Environ Sci Pollut Res Int. 2017 Oct;24(29):23015-23025. doi: 10.1007/s11356-017-9953-x. Epub 2017 Aug 19.
A number of methods have been reported for determining hydrophobic organic compound adsorption to dispersed carbon nanotubes (CNTs), but their accuracy and reliability remain uncertain. We have evaluated three methods to investigate the adsorption of phenanthrene (a model polycyclic aromatic hydrocarbon, PAH) to CNTs with different physicochemical properties: dialysis tube (DT) protected negligible depletion solid phase microextraction (DT-nd-SPME), ultracentrifugation, and filtration using various types of filters. Dispersed CNTs adhered to the unprotected polydimethylsiloxane (PDMS)-coated fibers used in nd-SPME. Protection of the fibers from CNT adherence was investigated with hydrophilic DT, but high PAH sorption to the DT was observed. The efficiency of ultracentrifugation and filtration to separate CNTs from the water phase depended on CNT physicochemical properties. While non-functionalized CNTs were efficiently separated from the water phase using ultracentrifugation, incomplete separation of carboxyl functionalized CNTs was observed. Filtration efficiency varied with different filter types (composition and pore size), and non-functionalized CNTs were more easily separated from the water phase than functionalized CNTs. Sorption of phenanthrene was high (< 70%) for three of the filters tested, making them unsuitable for the assessment of phenanthrene adsorption to CNTs. Filtration using a hydrophilic polytetrafluoroethylene (PTFE) filter membrane (0.1 μm) was found to be a simple and precise technique for the determination of phenanthrene adsorption to a range of CNTs, efficiently separating all types of CNTs and exhibiting a good and highly reproducible recovery of phenanthrene (82%) over the concentration range tested (70-735 μg/L).
已经有一些方法被报道用于测定分散的碳纳米管(CNTs)对疏水性有机化合物的吸附,但它们的准确性和可靠性仍不确定。我们已经评估了三种方法来研究具有不同物理化学性质的 CNTs 对菲(一种模型多环芳烃,PAH)的吸附:透析管(DT)保护的可忽略的耗尽固相微萃取(DT-nd-SPME)、超离心和使用各种类型的过滤器进行过滤。分散的 CNT 附着在 nd-SPME 中使用的未保护的聚二甲基硅氧烷(PDMS)涂层纤维上。通过亲水性 DT 研究了纤维对 CNT 附着的保护,但观察到高 PAH 对 DT 的吸附。超离心和过滤将 CNT 从水相分离的效率取决于 CNT 的物理化学性质。虽然非功能化的 CNT 可以通过超离心有效地从水相中分离出来,但羧基功能化的 CNT 则不完全分离。过滤效率随不同的滤器类型(组成和孔径)而变化,非功能化的 CNT 比功能化的 CNT 更容易从水相中分离出来。在所测试的三种过滤器中,菲的吸附率很高(<70%),因此它们不适合评估菲对 CNT 的吸附。使用亲水性聚四氟乙烯(PTFE)滤膜(0.1μm)进行过滤被发现是一种简单而精确的技术,可用于测定一系列 CNT 对菲的吸附,有效地分离所有类型的 CNT,并且对所测试的浓度范围(70-735μg/L)表现出良好且高度可重复的菲回收率(82%)。