University of Kentucky, College of Engineering, 512 Administration Drive, 177 F. Paul Anderson Tower, Lexington, KY 40506, USA.
Analyst. 2021 Jun 7;146(11):3599-3607. doi: 10.1039/d1an00144b. Epub 2021 Apr 30.
Due to mounting evidence of the negative health effects of persistent perfluoroalkyl acids (PFAAs) with long (i.e., >C) tails, there is a need for convenient systems capable of sensing these contaminants at dilute aqueous concentrations. To address this concern, a thermoresponsive polymeric network composed of poly(N-isopropylacrylamide) copolymerized with fluorinated comonomers was studied to characterize the gel's physical response to fluorosurfactants in solution. Incorporating fluorinated comonomers into the polymer backbone raised their swelling in fluorocontaminant solutions relative to water - gels synthesized with 10.0 mol% 2,2,2-trifluoroethyl acrylate (TFEA) displayed a heightened maximum water-analyte swelling difference of 3761 ± 147% compared to 3201 ± 466% for non-fluorinated gels in the presence of 1 mM tetraethylammonium perfluorooctane sulfonate (TPFOS). The normalized area under the curve for gels with 12.5 mol% TFEA was further raised to 1.77 ± 0.09, indicating a broadened response window for the contaminant, but at the cost of reducing the overall swelling ratio to 3227 ± 166% and elongating the time required to reach swelling equilibrium. Overall, a copolymer fed with 10.7 mol% TFEA was predicted to maximize both the swelling and response window of the polymer toward TPFOS. Equilibration times followed a logarithmic increase as the percentage of comonomer was raised, noting gradual fluorosurfactant penetration into the gels impeded by initial gel compaction caused by the addition of fluorinated comonomers. Comparative study of gels containing 1H,1H,7H-dodecafluoroheptyl acrylate, TFEA, or 1,1,1,3,3,3-hexafluoroisopropyl acrylate identified careful selection of fluorinated comonomers and their feed ratios as useful tools for tailoring the network's swelling response to TPFOS.
由于长链(即 >C)持久性全氟烷基酸(PFAAs)对健康的负面影响不断增加,因此需要能够在稀水溶液浓度下检测这些污染物的便捷系统。为了解决这个问题,研究了一种由聚(N-异丙基丙烯酰胺)与氟化共聚单体共聚而成的热响应聚合物网络,以表征凝胶对溶液中氟表面活性剂的物理响应。将氟化共聚单体引入聚合物主链会增加其在氟污染物溶液中的溶胀度-与不含氟的凝胶相比,用 10.0 mol% 2,2,2-三氟乙基丙烯酸酯(TFEA)合成的凝胶在 1 mM 四乙基铵全氟辛烷磺酸盐(TPFOS)存在下的最大水-分析物溶胀差异提高了 3761 ± 147%,而不含氟的凝胶为 3201 ± 466%。TFEA 为 12.5 mol%的凝胶归一化曲线下面积进一步提高到 1.77 ± 0.09,表明对污染物的响应窗口变宽,但代价是降低整体溶胀率至 3227 ± 166%,并延长达到溶胀平衡所需的时间。总的来说,预测共聚物中加入 10.7 mol% TFEA 可以使聚合物对 TPFOS 的溶胀和响应窗口最大化。平衡时间随着单体百分比的升高呈对数增加,这是由于氟化单体的加入导致初始凝胶压实,从而逐渐阻碍了氟表面活性剂渗透到凝胶中。含有 1H,1H,7H-十二氟庚基丙烯酸酯、TFEA 或 1,1,1,3,3,3-六氟异丙基丙烯酸酯的凝胶的比较研究表明,仔细选择氟化共聚单体及其进料比是调整网络对 TPFOS 溶胀响应的有用工具。