Institute of Biogeochemistry and Pollutant Dynamics (IBP), Department of Environmental Systems Science, Swiss Federal Institute of Technology, ETH Zurich , 8092 Zurich, Switzerland.
Environ Sci Technol. 2014 Aug 19;48(16):9420-9. doi: 10.1021/es5026917. Epub 2014 Aug 4.
Adlayers of dissolved organic matter (DOM) form on many surfaces in natural and engineered systems and affect a number of important processes in these systems. Yet, the nanoscalar properties and dynamics of DOM adlayers remain poorly investigated. This work provides a systematic analysis of the properties and dynamics of adlayers formed from a diverse set of eight humic and fulvic acids, used as DOM models, on surfaces of self-assembled monolayers (SAMs) of different alkylthiols covalently bound to gold supports. DOM adsorption to positively charged amine-terminated SAMs resulted in the formation of water-rich adlayers with nanometer thicknesses that were relatively rigid, irreversibly adsorbed, and collapsed upon air drying, as demonstrated by combined quartz crystal microbalance and ellipsometry measurements. DOM adlayer thicknesses varied only slightly with solution pH from 5 to 8 but increased markedly with increasing ionic strength. Contact angle measurements revealed that the DOM adlayers were relatively polar, likely due to the high water contents of the adlayers. Comparing DOM adsorption to SAM-coated sensors that systematically differed in surface charge and polarity characteristics showed that electrostatics dominated DOM-surface interactions. Laccase adsorption to DOM adlayers on amine-terminated SAMs served to demonstrate the applicability of the presented experimental approach to study the interactions of (bio)macromolecules and (nano)particles with DOM.
在自然和工程系统中,许多表面都会形成溶解有机物 (DOM) 的吸附层,这些吸附层会影响这些系统中的许多重要过程。然而,DOM 吸附层的纳米尺度性质和动力学仍未得到充分研究。本工作对一系列八种腐殖酸和富里酸形成的吸附层的性质和动力学进行了系统分析,这些腐殖酸和富里酸被用作 DOM 模型,在通过共价键结合到金基底的不同烷基硫醇自组装单层 (SAM) 表面上形成。带正电荷的胺端 SAM 对 DOM 的吸附导致形成具有纳米厚度的富含水的吸附层,这些吸附层相对较硬、不可逆吸附,并在空气干燥时坍塌,这一点通过石英晶体微天平和椭圆光度法的联合测量得到了证明。从 5 到 8,DOM 吸附层厚度随溶液 pH 值的变化很小,但随离子强度的增加而显著增加。接触角测量表明,DOM 吸附层具有相对极性,这可能是由于吸附层的含水量较高。比较 DOM 吸附到在表面电荷和极性特征上系统不同的 SAM 涂覆传感器表明,静电作用主导了 DOM-表面相互作用。漆酶吸附到胺端 SAM 上的 DOM 吸附层证明了所提出的实验方法可用于研究(生物)大分子和(纳米)颗粒与 DOM 的相互作用。