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Ion Transport in Temperature Sensitive Polyelectrolytes.

Record Type:	Language materials, manuscript : Monograph/item
Title/Author:	Ion Transport in Temperature Sensitive Polyelectrolytes./
Author:	Wang, Linghui.
Description:	1 online resource (127 pages)
Notes:	Source: Dissertations Abstracts International, Volume: 85-03, Section: B.
Contained By:	Dissertations Abstracts International85-03B.
Subject:	Medical equipment. -
Online resource:	click for full text (PQDT)
ISBN:	9798380277617

Ion Transport in Temperature Sensitive Polyelectrolytes.
Wang, Linghui.

Ion Transport in Temperature Sensitive Polyelectrolytes. - 1 online resource (127 pages)

Source: Dissertations Abstracts International, Volume: 85-03, Section: B.

Thesis (Ph.D.)--California Institute of Technology, 2023.

Includes bibliographical references

Temperature sensors are widely employed and play a key role in many industries, such as automotive vehicles, medical devices, environmental monitoring, and process control. The state-of-the-art thermal sensing elements are made of rigid and costly inorganic materials, such as vanadium oxide and platinum. These materials have limitations for emerging applications such as wearable devices and prosthetic devices. Ideal temperature sensing materials for such applications need to be flexible, reliable under mechanical deformation, and suitable for large-area production. Electrical conductive polymers were found to be a promising solution because of their flexibility and solution processability. However, they often lag in temperature resolution compared to their inorganic counterparts.A recent discovery revealed that the ionic conductivity of crosslinked pectin, a biopolymer extracted from plant cell walls, has a record-high temperature response. It is biocompatible, flexible when hydrated, and solution-processable, making it a strong candidate for wearable temperature sensing and conformal temperature mapping. However, open questions remain about the origin of its temperature sensitivity and the principles governing its ion transport. Furthermore, the heterogeneity of the complex molecular structure of pectin presents challenges to its integration in sensing devices.In this thesis, we study the origin of the high thermal sensitivity in pectin and develop a synthetic polyelectrolyte that mimics its key structure and properties. In Chapter 3, we focus on the ion transport mechanism in crosslinked pectin. We show that the binding between multivalent ions and certain chemical functional groups of pectin plays a critical role in its temperature sensitivity. In Chapter 4, the impact of water content on the ion transport and dielectric processes in crosslinked pectin is also investigated. In the following chapter, we present a novel synthetic polyelectrolyte designed to mimic pectin with a simpler structure. It has superior flexibility, high temperature sensitivity, and is stable under mechanical deformation. To further study this new material, we examine its ion transport dynamics under varying humidity and temperature conditions in Chapter 7. We discover that temperature and humidity have a similar effect on ion transport. Overall, we showed a biomimetic approach to design temperature sensitive polymers where the strong ion-polymer binding is the key to the ultrahigh temperature response.

Electronic reproduction.
Ann Arbor, Mich. :
ProQuest,
2024

Mode of access: World Wide Web

ISBN: 9798380277617Subjects--Topical Terms:

1437765
Medical equipment.
Index Terms--Genre/Form:

554714
Electronic books.

Ion Transport in Temperature Sensitive Polyelectrolytes.
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520 $a Temperature sensors are widely employed and play a key role in many industries, such as automotive vehicles, medical devices, environmental monitoring, and process control. The state-of-the-art thermal sensing elements are made of rigid and costly inorganic materials, such as vanadium oxide and platinum. These materials have limitations for emerging applications such as wearable devices and prosthetic devices. Ideal temperature sensing materials for such applications need to be flexible, reliable under mechanical deformation, and suitable for large-area production. Electrical conductive polymers were found to be a promising solution because of their flexibility and solution processability. However, they often lag in temperature resolution compared to their inorganic counterparts.A recent discovery revealed that the ionic conductivity of crosslinked pectin, a biopolymer extracted from plant cell walls, has a record-high temperature response. It is biocompatible, flexible when hydrated, and solution-processable, making it a strong candidate for wearable temperature sensing and conformal temperature mapping. However, open questions remain about the origin of its temperature sensitivity and the principles governing its ion transport. Furthermore, the heterogeneity of the complex molecular structure of pectin presents challenges to its integration in sensing devices.In this thesis, we study the origin of the high thermal sensitivity in pectin and develop a synthetic polyelectrolyte that mimics its key structure and properties. In Chapter 3, we focus on the ion transport mechanism in crosslinked pectin. We show that the binding between multivalent ions and certain chemical functional groups of pectin plays a critical role in its temperature sensitivity. In Chapter 4, the impact of water content on the ion transport and dielectric processes in crosslinked pectin is also investigated. In the following chapter, we present a novel synthetic polyelectrolyte designed to mimic pectin with a simpler structure. It has superior flexibility, high temperature sensitivity, and is stable under mechanical deformation. To further study this new material, we examine its ion transport dynamics under varying humidity and temperature conditions in Chapter 7. We discover that temperature and humidity have a similar effect on ion transport. Overall, we showed a biomimetic approach to design temperature sensitive polymers where the strong ion-polymer binding is the key to the ultrahigh temperature response.
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