Ion-Containing Polymers PDF Download
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Author: A. Eisenberg
Publisher: Elsevier
ISBN: 0323156754
Category : Science
Languages : en
Pages : 304
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Book Description
Ion-Containing Polymers: Physical Properties and Structure is Volume 2 of the series Polymer Physics. This book aims to fill in the gap in literature regarding the physical aspects of ion-containing polymers. A total of five chapters comprise this book. The Introduction (Chapter 1) generally deals with the application of ion-containing polymers, general classification, and the available works regarding the subject. Chapter 2 establishes the concepts of supermolecular structure and glass transitions in terms of the effects of ionic forces in polymers. These chapters provide the context in the discussion of viscoelastic properties of homopolymers and copolymers in Chapters 3 and 4. Finally, Chapter 5 tackles the configuration-dependent properties of ion-containing polymers. This volume will be of particular help to students in the field of physics and chemistry.
Author: A. Eisenberg
Publisher: Elsevier
ISBN: 0323156754
Category : Science
Languages : en
Pages : 304
Get Book Here
Book Description
Ion-Containing Polymers: Physical Properties and Structure is Volume 2 of the series Polymer Physics. This book aims to fill in the gap in literature regarding the physical aspects of ion-containing polymers. A total of five chapters comprise this book. The Introduction (Chapter 1) generally deals with the application of ion-containing polymers, general classification, and the available works regarding the subject. Chapter 2 establishes the concepts of supermolecular structure and glass transitions in terms of the effects of ionic forces in polymers. These chapters provide the context in the discussion of viscoelastic properties of homopolymers and copolymers in Chapters 3 and 4. Finally, Chapter 5 tackles the configuration-dependent properties of ion-containing polymers. This volume will be of particular help to students in the field of physics and chemistry.
Author: Adi Eisenberg
Publisher:
ISBN: 9780126649017
Category : Polymers
Languages : en
Pages : 287
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Book Description
Author: A. Eisenberg
Publisher:
ISBN:
Category :
Languages : en
Pages : 28
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Book Description
An extensive study of the properties of ionomers has been performed. One phase involved structure-property relations in styrene ionomers in which the placement of the ions, their type, and their concentration was varied systematically. Other variables involved changes in chain geometry. Also, a method was developed for compatibilizing otherwise immiscible polymers involving ionic interactions and finally, some studies were performed on Nafion membranes. (Author).
Author: Polymer Science Workshop. Polymer Science Workshop
Publisher:
ISBN:
Category : Polymers
Languages : en
Pages : 10
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Book Description
Author: Polymer Science Workshop
Publisher:
ISBN:
Category : Ionomers
Languages : en
Pages : 10
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Book Description
Author: Michel Pineri
Publisher:
ISBN:
Category : Ions
Languages : en
Pages : 10
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Book Description
Author: Michel Pineri
Publisher:
ISBN:
Category :
Languages : en
Pages : 10
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Book Description
Author: Joshua Enokida
Publisher:
ISBN:
Category :
Languages : en
Pages :
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Book Description
Ion-containing polymers are a unique class of materials for which strong electrostatic interactions dictate physical properties. By altering molecular parameters, such as the backbone chemical structure, the ion content, and the ion-pair identity, the structure and dynamics of these polymers can be altered. Further investigation of the molecular parameters that govern their structure-property relationships is critical for the future development of these polymeric materials. Particularly, the incorporation of ammonium-based counterions into these polymers offers a facile method to tune their electrostatic interactions and hydrophobicity. Applying this concept, a bulky dimethyloctylammonium (DMOA) counterion was used to modify the organic solubility of styrenesulfonate in order to facilitate its direct solution copolymerization with isoprene. With these poly(isoprene-ran-styrenesulfonate) (P(I-ran-SS)) copolymers the effect of ion content and the counterion identity on the structure and dynamics were evaluated. In the first project, poly(isoprene-ran-dimethyloctylammonium styrenesulfonate) (P(I-ran-DMOASS)) copolymers with high molecular weights and dimethyloctylammonium styrenesulfonate (DMOASS) compositions ranging between 8 and 40 mol% (30 - 77 wt%) were synthesized via nitroxide-mediated polymerization. Thermal and viscoelastic characterization revealed distinct behaviors for the low (30 - 51 wt%) and high (56 - 77 wt%) DMOASS content copolymers. Three structural regimes were identified: ion clusters (30 wt% DMOASS), continuous ionic phase (56 - 77 wt% DMOASS), and the coexistence of the two (42 - 51 wt% DMOASS). As DMOASS content increased, small angle X-ray scattering revealed a gradual transition from the characteristic ion cluster structure to a smaller, more regular backbone-backbone structure associated with a continuous ionic phase. The ion clusters acted as physical crosslinks and introduced additional elasticity into the low DMOASS content copolymer, while the continuous ionic phase showed restricted flow behavior and the disappearance of a definitive plateau modulus. Dynamic mechanical analysis revealed two distinct Tg's at intermediate DMOASS content, indicating the coexistence of both structures. In the second project, the role of counterion sterics on the structure and dynamics of a low glass transition temperature, amorphous P(I-ran-SS) at low ion contents (7 mol%) was investigated using a series of symmetric, tetraalkylammonium counterions with methyl (TMA), ethyl (TEA), propyl (TPA), and butyl (TBA) pendent groups in addition to a sodium cation control. A detailed analysis of the aggregate structure was achieved by fitting the X-ray scattering profiles with a modified hard sphere model. Increasing the counterion sterics from sodium to TEA resulted in slight changes to the aggregates with some ionic groups present in the isoprene matrix. For the more sterically hindered TPA and TBA counterions, considerable disruption of the structure occurs. Using solid-state NMR, dynamic mechanical analysis, and rheology, the effect of the counterion sterics on the copolymer dynamics was determined. The larger counterions exhibited an increase in the dynamic moduli at high frequency while decreasing the dynamic moduli at lower frequencies in addition to possessing faster molecular dynamics. These two observations correspond to the incorporation of more ionic groups into the isoprene matrix and weakening of the dipole-dipole interactions, respectively. Lastly, binary mixtures of TMA and TBA ammonium counterions were employed in these P(I-ran-SS) copolymers. The P(I-ran-SS) ionomers with TMA:TBA weight ratios of 100:0, 75:25, 50:50, 25:75, and 0:100 were prepared through solution blending. The SAXS profiles and Kinning-Thomas fitting showed only slight structural changes between 100:0 and 50:50, while major modification of the structure appears once the ratio reaches 75:25 and above. The alterations of the structure also indicated a mixed counterion aggregate structure. The linear viscoelastic characterization of the mixed counterion ionomers showed an increase in the polymer dynamics at low frequencies with increasing TBA weight percentages. Additionally, preliminary tensile tests were collected that showed increased mechanical properties with the stronger electrostatic interaction associated with TMA counterions. Thus, the structure and properties of these low Tg, amorphous ionomers can be specifically tuned by using multiple counterions. Through these studies, the role of both ion content and counterion identity on the structure and dynamics of low Tg, amorphous P(I-ran-SS) copolymers have been elucidated. Furthermore, ammonium-based cations have been shown to offer a versatile means to modify both the ion aggregate structure and interaction strength of an ionomer. Appropriate selection of the pendent groups and mixture of different counterions allow for the properties of the ionomer to be freely tuned.
Author: Yuan-Pang Samuel Ding
Publisher:
ISBN:
Category :
Languages : en
Pages : 344
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Book Description
Author: Michel Pineri
Publisher: Springer Science & Business Media
ISBN: 9400938292
Category : Science
Languages : en
Pages : 579
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Book Description
Ionomers, that is polymers containing a low concentration of charged units along the chain, have been the subject of increasing interest during the past twenty years. The presence of ionic groups in the poly mer changes some of its properties dramatically. Increases in the modu lus and the viscosity of several orders of magnitude have been observed, and changes in the glass transition of hundreds of degrees are possible. In addition, diffusion coefficients can be modified drastically. These changes are due primarily to the presence of reversible ionic cross links in these materials. Because of the low dielectric constant of most organic polymers, the ions or ionic dipoles tend to aggregate ; this aggregation process, however, is limited, because the ionic groups are covalently bonded to the organic chain. Host of the fundamental research done on these materials has been devoted to a determination of the extent of association, the structure of the aggregates, the limi ting factors, and the correlations between molecular and supermolecular structure and the resul ting properties.
