Download or read book Structure Property Relationships for Polymers Bearing Reversibly Associating Side groups written by Christopher Lloyd Lewis and published by . This book was released on 2014 with total page 237 pages. Available in PDF, EPUB and Kindle. Book excerpt: "The objective of this research is to establish structure-property relationships for macromolecules bearing reversibly associating side-groups. In previous studies we demonstrated shape-memory behavior for elastomer networks bearing strong ureido-pyrimidinone (UPy) hydrogen-bonding side-groups. However, relationships between the underlying viscoelastic behavior and side-group features such as hydrogen bond strength, structure, the presence of a permanent network and distance of the binding group from the macromolecular chain are not well established. Further, while numerous studies focus on the associative behavior of polymers in solution, few have examined their bulk behavior. To address this need, copolymers bearing weak ([Delta]H ~ 30kJ/mol) or strong hydrogen ([Delta]H ~ 70kJ/mol) bonding side-groups (HBSGs) were copolymerized with a low glass transition (Tg) polymer backbone into linear and network polymers. For polymers bearing weak HBSGs the temperature dependence of viscosity could be attributed to the elevation of Tg alone whereas the rheological behavior of strong HBSG polymers could be attributed to side-group association. To explain our results, a 'state-of-ease' model was developed that assumes continuous mechanical equilibrium between applied stress and the stresses arising from a permanent network and a second network that continuously reforms. The model is able to predict various rheological responses for UPy containing polymers such as dynamic mechanical and shape-memory behavior. The influence of micro-environment can also influence viscoelastic behavior. To assess the ability of a strong HBSG to dimerize within water swollen environments the swelling and dynamic mechanical behavior of a hydrophilic polymer bearing UPy side-groups was studied. The presence of UPy reduced the rate of short-time swelling whereas long-time swelling increased with UPy concentration and was attributed to UPy disrupting the native polymer structure. While the presence of UPy dramatically increased the viscosity, it does not form a percolated network at low UPy concentrations, suggesting that UPy's efficacy is reduced in the presence of water. In summary, by systematically studying several model polymers, this thesis exposes the degree to which reversibly binding side-groups can affect rheology, solid mechanics, and water sorption. The acquired knowledge can form a basis for materials design of future self-healing and shape-memory polymers, thermoplastic elastomers, and other field-responsive polymers"--Pages viii-ix.

Download or read book Structure Property Relationships in Polymers written by Charles E. Carraher Jr. and published by Springer Science & Business Media. This book was released on 2012-12-06 with total page 234 pages. Available in PDF, EPUB and Kindle. Book excerpt: The first concern of scientists who are interested in synthetic polymers has always been, and still is: How are they synthesized? But right after this comes the question: What have I made, and for what is it good? This leads to the important topic of the structure-property relations to which this book is devoted. Polymers are very large and very complicated systems; their character ization has to begin with the chemical composition, configuration, and con formation of the individual molecule. The first chapter is devoted to this broad objective. The immediate physical consequences, discussed in the second chapter, form the basis for the physical nature of polymers: the supermolecular interactions and arrangements of the individual macromolecules. The third chapter deals with the important question: How are these chemical and physical structures experimentally determined? The existing methods for polymer characterization are enumerated and discussed in this chapter. The following chapters go into more detail. For most applications-textiles, films, molded or extruded objects of all kinds-the mechanical and the thermal behaviors of polymers are of pre ponderant importance, followed by optical and electric properties. Chapters 4 through 9 describe how such properties are rooted in and dependent on the chemical structure. More-detailed considerations are given to certain particularly important and critical properties such as the solubility and permeability of polymeric systems. Macromolecules are not always the final goal of the chemist-they may act as intermediates, reactants, or catalysts. This topic is presented in Chapters 10 and 11.

Download or read book Structure property Relationships in Associating Polymer Solutions written by Eleftheria Antoniou and published by ProQuest. This book was released on 2008 with total page 0 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Download or read book Polymer Networks Containing Reversibly Associating Side groups written by Jiahui Li and published by . This book was released on 2011 with total page 380 pages. Available in PDF, EPUB and Kindle. Book excerpt: "Supramolecular polymers consist of low molar mass subunits that non-covalently bind together through hydrogen bonding or other non-covalent interactions, forming macromolecular assemblies. Site-specific and reversible hydrogen bonds and other non-covalent interactions are increasingly employed to modify bulk polymer properties, enabling thermoplastic elastomers and self-healing polymers. In this thesis, I investigate how hydrogen bonding groups directly bonded onto an elastic polymer network affect material properties. A lightly crosslinked covalent network containing hydrogen bonding side-groups (ureidopyrimidinone, UPy) was synthesized. This architecture results in a novel shape-memory effect, and the molecular events resulting in this behavior were deduced. Further, to systematically evaluate how thermomechanical properties are related to network architecture, a new photo-crosslinking route was developed to prepare shape-memory elastomers. This method enables melt-processing of shape-memory elastomers into complex permanent shapes, and samples can be prepared with much higher UPy-content. Furthermore, the covalent and non-covalent crosslink density can be accurately controlled. Dynamic mechanical analysis on photo-crosslinked shape-memory elastomers revealed that dynamic crosslinks behave nearly as effectively as permanent crosslinks below the UPy hydrogen bond transition. Compared to linear polymers bearing identical hydrogen bonding groups, the synthesized dynamic networks exhibit an enhanced temperature dependence of mechanical properties. This indicates that the covalent network supports cooperative hydrogen bonding. This finding will guide researchers to more effectively employ non-covalent interactions within bulk polymer materials. Mass transport through dynamic networks was also studied using multi-photon fluorescence recovery after photobleaching (MP-FRAP). In contrast to viscous relaxation, small molecule mass transport through the dynamic networks is limited by the density of hydrogen bonds instead of their exchange rate"--Leaves vii-viii.

Download or read book Structure property Relationships in Polymers written by E. H. Andrews and published by . This book was released on 1988 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt:

Download or read book Structure property Relationships in Physical Polymer Gels written by Michelle Kay Sing and published by . This book was released on 2017 with total page 354 pages. Available in PDF, EPUB and Kindle. Book excerpt: Associating polymer networks are included in a large number of materials where it is important to control and tune the rheological response of the material, particularly including responses to temperature, shear, or changes in the surrounding environment. Knowledge of the relationship between the kinetics of the end-groups that form these associations and the mechanical behavior of the network can provide valuable insight into the design of these sorts of materials. This thesis first looks at a simple theoretical approach for predicting the mechanical behavior of these transient networks as a function of the association kinetics. By using a modified form of the Smoluchowski equation to track the full probability distribution of looped, bridged, and dangling chain conformations in the network, it is possible to see relationships between the rate at which chains associate and dissociate and the presence of non-monotonic flow behaviors. Dangling chain tumbling due to the internal flux of the system under shear resulted in decreased stress through the ability to then form looped chains. The Smoluchowski equation can be adjusted to its Langevin form for Brownian Dynamics simulations of chain ends as a function of location and conformation. This modified formalism makes it so that it is not only striaghtforward to extract network relaxation times as a function of relative kinetics, but it is also possible to incorporate multiple bonds within a single association such that the association has a constant bond energy regardless of the number of bonds. The network relaxation can be grouped into two cases - one where a dissociated dangling chain is able to fully relax prior to association, and the other where the chain can only relax a fraction of the way prior to reassociation. These two cases result in different numbers of characteristic network relaxation times that change with increasing bond number. The second part of this thesis focuses on experimentally investigating how block and sequence architecture affect the deformation behavior and kinetics of thermoresponsive, dual-associating block copolymer systems. These systems are comprised of thermoresponsive elastin-like polypeptide endblocks (ELPs) fused to a polypeptide containing self-associating a-helical domains. Above the critical gel concentration, these protein fusions form disordered spherical nanostructures in solution. In shear flow, the rate of network deformation and rearrangement could be increased or decreased by changing block architecture, temperature, or concentration of the system. Protein fusions containing the standard ELP sequence underwent a liquid-like rearrangement of the nanostructure to accommodate the shear stresses associated with flow. Performing an amino acid substitution in the ELP endblock further affected the kinetics of rearrangement and resulted in multiple orders of magnitude increases in material toughness. This thesis has provided an increased understanding of how tailoring the properties of endblock associations can affect the mechanical behavior of the bulk material. Through increased understanding of how the properties of associating groups affect the macroscopic material properties, it is possible to better inform materials design for end-use applications.

Download or read book Hydrophobically Associating Polymers written by Andrew Robert Hirst and published by . This book was released on 2001 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt:

Download or read book Structure property Relationships in Side Chain Liquid Crystal Polymers written by Aileen A. Craig and published by . This book was released on 1996 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt:

Download or read book Structure property Relationships in Dynamic Polymer Networks written by Christopher Brittain Cooper and published by . This book was released on 2023 with total page 0 pages. Available in PDF, EPUB and Kindle. Book excerpt: Many emerging applications including wearable electronics and e-skins, soft robotics and actuators, and biomaterials, require material platforms with precisely controlled mechanical, electrical, thermal, and optical properties. The practical realization of devices for these applications is often restricted not by the lack of novel designs, but rather by the sparsity of materials with the required properties. Dynamic polymers, which employ both permanent and reversible linkages, offer a promising platform for the design of new materials due to their highly tunable and responsive chemical structures. This dissertation explores structure-property relationships in different dynamic polymer networks with well-defined polymer design and is structured as follows. Chapter 1 introduces the concept of dynamic polymers, provides comparisons to supramolecular polymers and segmented block copolymers, and concludes with emerging applications for these systems. Chapter 2 examines the molecular design rules for spontaneous self-assembly of periodic dynamic polymers into supramolecular nanofibers. Chapter 3 discusses the phenomenon of strain-induced supramolecular structures exhibited by entangled periodic dynamic polymers. Chapter 4 highlights how the clustered nanomorphology exhibited by periodic dynamic polymers can be used to design recyclable underwater adhesives. Chapter 5 explains how immiscible dynamic polymers can be used to achieve autonomous alignment of multilayered soft electronics. Chapter 6 concludes with key observations and on the future outlook of next-generation materials.

Download or read book Structure Property Relationships in Polymer Systems From Functional Microgels to Dynamic Polymer Solutions and Melts written by Willi Schmolke and published by . This book was released on 2020 with total page 0 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Download or read book Structure and Rheological Properties of Self associating Polymer Networks written by and published by . This book was released on 2015 with total page 64 pages. Available in PDF, EPUB and Kindle. Book excerpt: Self-associating polymers have become a key component within modern material science. The ability of the molecule to add complex material properties has spawned interest in a multitude of applications, including a wide variety of consumer products and most recently within themedical field. Fluid-like viscosity to near solid-like elastic dynamics can be observed within polymeric materials. Relatively small changes in external parameters can result in large transitions in this behavior. The concentration of polymers within solution, the temperature of the material, and the lifetime between the attractive chemical groups are a few factors that contribute to their general properties. Despite being widely utilized, how these systems deform under external stresses and exhibit such a wide range of properties is still poorly understood. The following manuscript describes numerical studies where the response of associating polymers to shear deformation is explored. A computational model using a novel, hybrid molecular dynamics, Monte Carlo (MC) algorithm is employed. Polymer chains are modeled as course-grained, bead-spring systems. The attractive end groups form reversible, physical bonds according to MC rules. At high temperatures the system is shown to behave as a fluid. Decreasing the temperature results in self-assembly, forming a complex network structure that is transient. The nodes of this network consist of aggregates of end groups, while links between aggregates are formed by one or more bridging polymer chains. The aggregation dynamics of end groups vary with temperature and time. As a result, aggregate sizes change frequently throughout the simulation. Master equations are employed, defining changes in the number of aggregates of a certain size in terms of reaction rates. Variations in these rates are shown to give rise to the observed changes in the aggregate distribution that characterizes the transition between fluid to solid-like dynamics. Rheological experiments are then performed to obtain the system's stress response to shear deformation. Studies provide insight on microstructural variations in the network topology that lead to observed phenomena within experimental systems. Data obtained in both the linear and nonlinear regimes are then correlated with observed changes in the material properties.

Download or read book Structure property Relationships of ROMP Polymers written by Marlene Elaine Hontz and published by . This book was released on 2000 with total page 428 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Download or read book Structure property Relationships in Polymers of 2 3 Dichlorobutadiene written by Mark Alfred Weih and published by . This book was released on 1991 with total page 732 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Download or read book Structure property Relationships of Some Polymer Blends written by Yong-Won Kim and published by . This book was released on 1989 with total page 254 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Download or read book Structure property Relationships in Thiol based Polymer Networks written by Michael Taylor and published by . This book was released on 2001 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt:

Download or read book Structure Property Relationships in Polymer Systems From Functional Microgels to Dynamic Polymer Solutions and Melts written by Willi Schmolke and published by . This book was released on 2020 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt:

Download or read book Study of the Structure property Relationships of Polymers with Metal ligand Coordination Bonds written by Xinyue Zhang and published by . This book was released on 2022 with total page 0 pages. Available in PDF, EPUB and Kindle. Book excerpt: Incorporating dynamic interactions into polymer matrices has emerged as a powerful tool to engineer materials for advanced applications. Metal-ligand coordination as the dynamic component has been a popular choice due to the diversity and ease of tailoring the functional sites without altering the backbone chemistry. Extensive theoretical and experimental studies have been conducted to unveil the fundamental science and critical mechanisms for better material design. The sticky Rouse model has been developed to describe the linear viscoelasticity of associative polymers neglecting the chemistry and structural details of bonding sites. Most of the experimental research on polymers containing metal-ligand coordination has focused on synthesis methods or the optical and mechanical effects resulting from bonds breaking and reforming. A gap between the theoretical understanding and the experimental findings exists due to the challenge of decoupling the metal-ligand interactions from other factors governing the bulk polymer behavior. In addition, the dynamic surface properties and ionic conductivity performances arising from metal-ligand coordination are less studied. This dissertation contributes to the understanding of the structure-property relationships of metal-ligand coordinated polymers by bridging the molecular metal-ligand coordination details and the macroscopic behavior of the materials with carefully designed model systems. This dissertation starts with a combined experimental and theoretical approach to quantitatively establishing how the stability and structure of metal-ligand interaction acting as dynamic crosslinks determines the viscoelastic characteristics of a metallopolymer. A model system which is free from solvent molecules, chain entanglement and phase-separation was designed to decouple the metal-ligand interactions from other factors governing the polymer behavior. By analyzing the key parameters extracted from the experimental results, the enhanced sticky Rouse model was proposed. This assists subsequent rational design of metal-ligand coordinated polymers with an easily accessible and implementable quantitative model. We then moved on to demonstrate that introducing metal-ligand coordination not only enables the dynamic characteristics of the polymer, but also raises other fascinating properties. This idea was elaborated in the following two works. First, we proposed a surface design approach to enable a reversible transition between hydrophobicity and hydrophilicity on the polymer surface in response to changing the environment polarity via "hiding" polar metal-ligand coordination sites under non-polar PDMS backbone. The dynamic characteristics of the bulk polymer is governed by network architecture and coordination strength, and is directly correlated to the speed and extent of the surface evolution. Second, we investigated the ionic conductivity of metal-ligand coordinated PDMS. The interaction between the ligands on a polymer chain and the metal cations from the salt added facilities the ion dissociation within the PDMS, and turns the non-conductive PDMS into an ionic conductive PDMS. The ionic transport mechanism was discussed in the context of the density and strength of metal-ligand coordination. Synergistic effects were observed and discussed for mixed lithium (Li) and copper (Cu) coordination, which shows the improved mechanical strength as well as ionic conductivity compared to the Li-coordinated PDMS. The systematic study on the structure-property relationships of polymers containing metal-ligand coordination in this dissertation provides insights to assist the design of advanced materials.