Suppr超能文献

二价阳离子对聚(二烯丙基二甲基氯化铵)-聚(苯乙烯磺酸盐)聚电解质复合物玻璃化转变的影响。

Divalent cation effects in the glass transition of poly(diallyldimethylammonium)-poly(styrene sulfonate) polyelectrolyte complexes.

作者信息

Braide Tamunoemi, Manoj Lalwani Suvesh, Eneh Chikaodinaka I, Lutkenhaus Jodie L

机构信息

Artie McFerrin Department of Chemical Engineering, Texas A&M University, College Station, Texas 77840, USA.

Department of Materials Science and Engineering, Texas A&M University, College Station, Texas 77840, USA.

出版信息

Soft Matter. 2024 Dec 11;20(48):9631-9641. doi: 10.1039/d4sm00856a.

Abstract

The assembly and dynamics of polyelectrolyte complexes (PECs) and polyelectrolyte multilayers (PEMs) are influenced by water content, pH, and salt concentration. However, the influence of divalent salts on the assembly of polyelectrolyte complexes remains unclear. This work showcases that divalent chloride salts directly impact the glass transition temperature and the ion-ion interactions within PECs. Here, poly(diallyldimethylammonium)-poly(styrene sulfonate) (PDADMA-PSS) PECs are assembled in solutions containing MgCl and CaCl (following the Hofmeister series). These PECs are studied for the cations' influence on physicochemical properties (glass transition, polymer composition, ion pairing) at varying salt concentrations (0.03 M, 0.10 M, 0.15 M, and 0.20 M). Modulated differential scanning calorimetry (MDSC) experiments demonstrate that PECs assembled with CaCl have a significantly higher glass transition temperature when compared to PECs assembled with MgCl. Neutron activation analysis (NAA) and nuclear magnetic resonance (NMR) spectroscopy demonstrate that this difference is due to strong ion-specific effects influencing the ratio of intrinsic and extrinsic ion pairings in the system. Furthermore, this study demonstrates a universal linear relationship between the thermal transition and the number of water molecules surrounding oppositely charged polyelectrolyte-polyelectrolyte intrinsic ion pairs, even when the salt contains divalent cations. Ion-specific trends have implications on the glass transition and composition of PDADMA-PSS PECs. Divalent salts not only follow the trend of the Hofmeister series but also introduce bridging into the polyelectrolyte complex; however, the structural relaxation of the PEC remains the same. This study offers a bridge between divalent cation behavior on polymer assembly properties and its transition to industrial applications such as controlled drug delivery, sensors, and water purification.

摘要

聚电解质复合物(PEC)和聚电解质多层膜(PEM)的组装及动力学受含水量、pH值和盐浓度的影响。然而,二价盐对聚电解质复合物组装的影响仍不明确。这项工作表明,二价氯化物盐直接影响PEC内的玻璃化转变温度和离子-离子相互作用。在此,聚(二烯丙基二甲基氯化铵)-聚(苯乙烯磺酸盐)(PDADMA-PSS)PEC在含有MgCl和CaCl的溶液中组装(遵循霍夫迈斯特序列)。研究了这些PEC在不同盐浓度(0.03 M、0.10 M、0.15 M和0.20 M)下阳离子对其物理化学性质(玻璃化转变、聚合物组成、离子配对)的影响。调制差示扫描量热法(MDSC)实验表明,与用MgCl组装的PEC相比,用CaCl组装的PEC具有显著更高的玻璃化转变温度。中子活化分析(NAA)和核磁共振(NMR)光谱表明这种差异是由于强烈的离子特异性效应影响了系统中固有和外在离子配对的比例。此外,这项研究表明,即使盐中含有二价阳离子,热转变与带相反电荷的聚电解质-聚电解质固有离子对周围水分子的数量之间也存在普遍的线性关系。离子特异性趋势对PDADMA-PSS PEC的玻璃化转变和组成有影响。二价盐不仅遵循霍夫迈斯特序列的趋势,还会在聚电解质复合物中引入桥连;然而,PEC的结构弛豫保持不变。这项研究为二价阳离子在聚合物组装性质方面的行为与其向工业应用(如控释药物、传感器和水净化)的转变之间架起了一座桥梁。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验