Department of Chemistry, Washington University in Saint Louis, One Brookings Drive, Saint Louis, Missouri 63130-4899, USA.
ACS Appl Mater Interfaces. 2011 Jun;3(6):2118-29. doi: 10.1021/am200337q. Epub 2011 Jun 6.
A series of thiol-ene generated amphiphilic cross-linked networks was prepared by reaction of alkene-modified Boltorn polyesters (Boltorn-ene) with varying weight percent of 4-armed poly(ethylene glycol) (PEG) tetrathiol (0-25 wt%) and varying equivalents of pentaerythritol tetrakis(3-mercaptopropionate) (PETMP) (0-64 wt%). These materials were designed to present complex surface topographies and morphologies, with heterogeneity of surface composition and properties and robust mechanical properties, to serve as nontoxic antibiofouling coatings that are amenable to large-scale production for application in the marine environment. Therefore, a two-dimensional matrix of materials compositions was prepared to study the physical and mechanical properties, over which the compositions spanned from 0 to 25 wt% PEG tetrathiol and 0-64 wt% PETMP (the overall thiol/alkene (SH/ene) ratios ranged from 0.00 to 1.00 equiv), with both cross-linker weight percentages calculated with respect to the weight of Boltorn-ene. The Boltorn-ene components were prepared through the esterification of commercially available Boltorn H30 with 3-butenoic acid. The subsequent cross-linking of the Boltorn-PEG-PETMP films was monitored using IR spectroscopy, where it was found that near-complete consumption of both thiol and alkene groups occurred when the stoichiometry was ca. 48 wt% PETMP (0.75 equiv SH/ene, independent of PEG amount). The thermal properties of the films showed an increase in T(g) with an increase in 4-armed PEG-tetrathiol wt%, regardless of the PETMP concentration. Investigation of the bulk mechanical properties in dry and wet states found that the Young's modulus was the greatest at 48 wt% PETMP (0.75 equiv of SH/ene). The ultimate tensile strength increased when PETMP was constant and the PEG concentration was increased. The Young's modulus was slightly lower for wet films at constant PEG or constant PETMP amounts, than for the dry samples. The nanoscopic surface features were probed using atomic force microscopy (AFM), where it was observed that the surface of the amphiphilic films became increasingly rough with increasing PEG wt%. On the basis of the physicochemical data from the diverse sample matrix, a focused compositional profile was then investigated further to determine the antifouling performance of the cross-linked Boltorn-PEG-PETMP networks. For these studies, a low, constant PETMP concentration of 16 wt% was maintained with variation in the PEG wt% (0-35 wt%). Antifouling and fouling-release activities were tested against the marine alga Ulva. Spore settlement densities were low on these films, compared to that on standards of polydimethylsiloxane and glass.
一系列巯基-烯生成的两亲性交联网络通过烯基改性的 Boltorn 聚酯(Boltorn-ene)与不同重量百分比的 4 臂聚(乙二醇)(PEG)四巯基(0-25wt%)和不同当量的季戊四醇四(3-巯基丙酸酯)(PETMP)(0-64wt%)反应制备。这些材料旨在呈现复杂的表面形貌,具有表面组成和性质的不均匀性以及坚固的机械性能,可用作无毒的抗生物污染涂层,可大规模生产,适用于海洋环境。因此,制备了一个二维材料组成矩阵,以研究物理和机械性能,其中组成范围从 0 到 25wt%PEG 四巯基和 0-64wt%PETMP(总巯基/烯基(SH/ene)比为 0.00 至 1.00 当量),两种交联剂的重量百分比均相对于 Boltorn-ene 的重量计算。Boltorn-ene 成分通过商业上可用的 Boltorn H30 与 3-丁烯酸的酯化制备。随后使用红外光谱监测 Boltorn-PEG-PETMP 薄膜的交联,结果发现当化学计量比约为 48wt%PETMP(0.75 当量 SH/ene,与 PEG 量无关)时,几乎完全消耗了巯基和烯基。薄膜的热性能显示出 T(g)随 4 臂 PEG-四巯基重量百分比的增加而增加,而与 PETMP 浓度无关。在干燥和湿润状态下对块状力学性能的研究发现,在 48wt%PETMP(0.75 当量 SH/ene)时杨氏模量最大。当 PETMP 保持恒定时,PEG 浓度增加时,极限拉伸强度增加。对于恒定 PEG 或恒定 PETMP 量的湿膜,杨氏模量略低于干样。使用原子力显微镜(AFM)探测纳米级表面特征,观察到随着 PEG 重量百分比的增加,两亲性薄膜的表面变得越来越粗糙。基于来自不同样品矩阵的物理化学数据,然后进一步研究了聚焦的组成分布,以确定交联 Boltorn-PEG-PETMP 网络的抗污染性能。在这些研究中,保持 PETMP 的低、恒定浓度为 16wt%,同时变化 PEGwt%(0-35wt%)。抗污染和防污释放活性针对海洋藻类 Ulva 进行了测试。与聚二甲基硅氧烷和玻璃的标准相比,这些薄膜上的孢子沉降密度较低。