CREPEC, Department of Chemical Engineering , Polytechnique Montréal , C.P. 6079 Succursale Centre-Ville , Montréal , Québec H3C 3A7 , Canada.
ACS Appl Mater Interfaces. 2018 Jun 27;10(25):21073-21078. doi: 10.1021/acsami.8b06560. Epub 2018 Jun 15.
This work demonstrates that a model system of poly( N-isopropylacrylamide) (PNIPAam) macroporous hydrogels, with tailored microstructures and comprising gold (Au) or silver (Ag) nanoparticles, display enhanced and tunable catalytic activity. These nanocomposites are prepared using polymer templates obtained from melt-processed cocontinuous polymer blends. The reaction rate, controlled by both hydrogel porosity and the PNIPAam lower critical solution temperature, increases by more than an order of magnitude as compared to nonporous gels, and is comparable to micro- or nanocarrier-based systems, with easier catalyst recovery. The fabrication process is scalable, and is compatible with broad choices of polymer blend, gel, and nanoparticle chemistries.
这项工作表明,具有定制微观结构且包含金(Au)或银(Ag)纳米粒子的聚(N-异丙基丙烯酰胺)(PNIPAam)大孔水凝胶模型系统具有增强和可调的催化活性。这些纳米复合材料是使用从熔融共连续聚合物共混物获得的聚合物模板制备的。反应速率受水凝胶孔隙率和 PNIPAam 低临界溶液温度的共同控制,与无孔凝胶相比,增加了一个数量级以上,与基于微载体或纳米载体的系统相当,并且催化剂更容易回收。制造工艺具有可扩展性,并且与聚合物共混物、凝胶和纳米颗粒化学的广泛选择兼容。