Laboratory of Physical Chemistry and Colloid Science, Wageningen University , Dreijenplein 6, 6703 HB Wageningen, The Netherlands.
Langmuir. 2014 Mar 4;30(8):2084-92. doi: 10.1021/la4050094. Epub 2014 Feb 19.
The partitioning of the natural polyelectrolyte humic acid (HA) from an aqueous dispersion into a model biomimetic gel (alginate) and a synthetic polyacrylamide gel (PAAm) is explored. In both gels, the spatial distribution of HA in the gel body, as measured by confocal laser scanning microscopy, is markedly nonhomogeneous. A striking feature is the enhanced accumulation of HA in a thin film of thickness ca. 15 μm at the surface of the gel body, resulting in average local concentrations that are, for PAAm and alginate respectively, a factor of 10 and 4 greater than that in the bulk solution. The time dependence of accumulation in the surface film is predominantly controlled by the diffusive supply of HA from the aqueous medium, with a time constant on the order of 10(3) s for both gels. The concentration of HA within the bulk gel body differs significantly from that in the bulk aqueous medium: substantially higher for PAAm but much lower for alginate. The results are significant for understanding the nature and rate of sink/source functioning at permeable phases in contact with aqueous media, e.g., biofilms and gel-like layers at biological interfaces or employed in chemical speciation sensors.
探索了天然高分子电解质腐殖酸(HA)从水相分散体分配到模型仿生凝胶(藻酸盐)和合成聚丙烯酰胺凝胶(PAAm)中的情况。在这两种凝胶中,通过共聚焦激光扫描显微镜测量,HA 在凝胶体中的空间分布明显不均匀。一个显著的特点是,HA 在凝胶体表面约 15μm 厚的薄膜中强烈积累,导致局部平均浓度分别比本体溶液高 10 倍和 4 倍。在表面膜中的积累的时间依赖性主要由从水介质中扩散供应的 HA 控制,对于两种凝胶,时间常数约为 10(3) s。HA 在本体凝胶体中的浓度与本体水溶液中的浓度显著不同:对于 PAAm 来说要高得多,但对于藻酸盐来说要低得多。这些结果对于理解与水相接触的可渗透相中的汇/源功能的性质和速率非常重要,例如生物膜和生物界面上的凝胶状层或用于化学形态传感器。