Moulton James T, Bruce David, Bunce Richard A, Kim Mariya, Snyder Leah Oxenford, Seitz W Rudolf, Lavine Barry K
Department of Chemistry, Oklahoma State University, Stillwater, OK 74078, USA.
Department of Chemistry, University of New Hampshire, Durham, NH 03824, USA.
Molecules. 2025 Mar 22;30(7):1416. doi: 10.3390/molecules30071416.
Copolymers of -isopropylacrylamide (NIPA) and alkyl acrylic acids that swell and shrink in response to pH were prepared by dispersion polymerization at 35 °C using -isopropylacrylamide (transduction monomer), methylenebisacrylamide (crosslinker), 2-dimethoxy-2-phenyl-acetophenone (initiator), --butylacrylamide (transition temperature modifier), and acrylic acid, methacrylic acid, ethacrylic acid, and propacrylic acid (functional comonomer). The diameter of the microspheres of the copolymer varied between 0.5 µm and 1.0 µm. These microspheres were cast into hydrogel membranes prepared by mixing the pH-sensitive swellable polymer particles with aqueous polyvinyl alcohol solutions followed by crosslinking the polyvinyl alcohol with glutaric dialdehyde for use as pH sensors. Large changes in the turbidity of the polyvinyl alcohol membrane monitored using a Cary 6000 UV-visible absorbance spectrometer were observed as the pH of the buffer solution in contact with the membrane was varied. Polymer swelling was reversible for many of these NIPA-based copolymers. The buffer capacity, ionic strength, pH, and temperature of the buffer solution in contact with the membrane were systematically varied to provide an in-depth pH profile of each copolymer. A unique aspect of this study was the investigation of the response of the NIPA-based polymers to changes in the pH of the solution in contact with the membrane at low buffer concentrations (0.5 mM). The response rate and the reversibility of polymer swelling even at low buffer capacity suggest that NIPA-based copolymers can be coupled to an optical fiber for pH sensing in the environment. We envision using these polymers to monitor rising acidity levels in the ocean due to water that has become enriched in carbon dioxide that endangers shell-building organisms by reducing the amount of carbonate available to them.
通过分散聚合反应,在35℃下使用N - 异丙基丙烯酰胺(转导单体)、亚甲基双丙烯酰胺(交联剂)、2 - 二甲氧基 - 2 - 苯基苯乙酮(引发剂)、N - 丁基丙烯酰胺(转变温度调节剂)以及丙烯酸、甲基丙烯酸、乙基丙烯酸和丙基丙烯酸(功能性共聚单体)制备了对pH响应而溶胀和收缩的N - 异丙基丙烯酰胺(NIPA)与烷基丙烯酸的共聚物。该共聚物微球的直径在0.5微米至1.0微米之间变化。将这些微球浇铸到水凝胶膜中,该水凝胶膜是通过将对pH敏感的可溶胀聚合物颗粒与聚乙烯醇水溶液混合,然后用戊二醛交联聚乙烯醇而制备的,用作pH传感器。当与膜接触的缓冲溶液的pH发生变化时,使用Cary 6000紫外可见吸收光谱仪监测到聚乙烯醇膜的浊度发生了很大变化。对于许多这些基于NIPA的共聚物,聚合物溶胀是可逆的。系统地改变与膜接触的缓冲溶液的缓冲容量、离子强度、pH和温度,以提供每种共聚物的深入pH分布图。这项研究的一个独特之处在于,研究了基于NIPA的聚合物在低缓冲浓度(0.5 mM)下对与膜接触的溶液pH变化的响应。即使在低缓冲容量下,聚合物溶胀的响应速率和可逆性表明,基于NIPA的共聚物可与光纤耦合用于环境中的pH传感。我们设想使用这些聚合物来监测海洋中酸度水平的上升,这是由于水中二氧化碳含量增加所致,二氧化碳会减少可供造壳生物利用的碳酸盐量,从而危及这些生物。