聚(二烯丙基二甲基铵)-聚(苯乙烯磺酸盐)聚电解质复合物玻璃化转变中的二价阳离子效应。

IF 2.9 3区 化学 Q3 CHEMISTRY, PHYSICAL
Soft Matter Pub Date : 2024-11-26 DOI:10.1039/d4sm00856a
Tamunoemi Braide, Suvesh Manoj Lalwani, Chikaodinaka I Eneh, Jodie L Lutkenhaus
{"title":"聚(二烯丙基二甲基铵)-聚(苯乙烯磺酸盐)聚电解质复合物玻璃化转变中的二价阳离子效应。","authors":"Tamunoemi Braide, Suvesh Manoj Lalwani, Chikaodinaka I Eneh, Jodie L Lutkenhaus","doi":"10.1039/d4sm00856a","DOIUrl":null,"url":null,"abstract":"<p><p>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<sub>2</sub> and CaCl<sub>2</sub> (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<sub>2</sub> have a significantly higher glass transition temperature when compared to PECs assembled with MgCl<sub>2</sub>. 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.</p>","PeriodicalId":103,"journal":{"name":"Soft Matter","volume":" ","pages":""},"PeriodicalIF":2.9000,"publicationDate":"2024-11-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Divalent cation effects in the glass transition of poly(diallyldimethylammonium)-poly(styrene sulfonate) polyelectrolyte complexes.\",\"authors\":\"Tamunoemi Braide, Suvesh Manoj Lalwani, Chikaodinaka I Eneh, Jodie L Lutkenhaus\",\"doi\":\"10.1039/d4sm00856a\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>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<sub>2</sub> and CaCl<sub>2</sub> (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<sub>2</sub> have a significantly higher glass transition temperature when compared to PECs assembled with MgCl<sub>2</sub>. 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.</p>\",\"PeriodicalId\":103,\"journal\":{\"name\":\"Soft Matter\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":2.9000,\"publicationDate\":\"2024-11-26\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Soft Matter\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1039/d4sm00856a\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Soft Matter","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1039/d4sm00856a","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0

摘要

聚电解质复合物(PEC)和聚电解质多层膜(PEM)的组装和动力学受含水量、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清楚。这项研究表明,二价氯盐会直接影响聚电解质复合物的玻璃化转变温度和离子间的相互作用。在这里,聚(二烯丙基二甲基铵)-聚(苯乙烯磺酸盐)(PDADMA-PSS)PECs 是在含有 MgCl2 和 CaCl2 的溶液中组装的(按照霍夫迈斯特系列)。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)下阳离子对物理化学特性(玻璃化转变、聚合物成分、离子配对)的影响。调制差示扫描量热法(MDSC)实验表明,与使用氯化镁组装的 PEC 相比,使用氯化钙组装的 PEC 的玻璃化转变温度明显更高。中子活化分析 (NAA) 和核磁共振 (NMR) 光谱证明,这种差异是由于强烈的离子特异性效应影响了系统中内在和外在离子配对的比例。此外,本研究还证明了热转变与围绕带对立电荷的聚电解质-聚电解质本征离子对的水分子数量之间的普遍线性关系,即使盐中含有二价阳离子也是如此。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系列的趋势,而且还在聚电解质复合物中引入了桥接;但是,聚电解质的结构松弛保持不变。这项研究在二价阳离子对聚合物组装特性的影响及其向工业应用(如受控药物输送、传感器和水净化)的过渡之间架起了一座桥梁。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Divalent cation effects in the glass transition of poly(diallyldimethylammonium)-poly(styrene sulfonate) polyelectrolyte complexes.

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 MgCl2 and CaCl2 (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 CaCl2 have a significantly higher glass transition temperature when compared to PECs assembled with MgCl2. 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.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Soft Matter
Soft Matter 工程技术-材料科学:综合
CiteScore
6.00
自引率
5.90%
发文量
891
审稿时长
1.9 months
期刊介绍: Where physics meets chemistry meets biology for fundamental soft matter research.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信