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Book Synthesis of Amphipathic Block Copolymers Based on Polyisobutylene and Polyoxyethylene and Their Application in Emulsion Polymerization

Download or read book Synthesis of Amphipathic Block Copolymers Based on Polyisobutylene and Polyoxyethylene and Their Application in Emulsion Polymerization written by Bidulata Sar and published by . This book was released on 1993 with total page 380 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Book Amphiphilic Block Copolymers

Download or read book Amphiphilic Block Copolymers written by P. Alexandridis and published by Elsevier. This book was released on 2000-10-18 with total page 449 pages. Available in PDF, EPUB and Kindle. Book excerpt: It is the belief of the editors of this book that the recognition of block copolymers as being amphiphilic molecules and sharing common features with other well-studied amphiphiles will prove beneficial to both the surfactant and the polymer communities. An aim of this book is to bridge the two communities and cross-fertilise the different fields. To this end, leading researchers in the field of amphiphilic block copolymer self-assembly, some having a background in surfactant chemistry, and others with polymer physics roots, have agreed to join forces and contribute to this book.The book consists of four entities. The first part discusses theoretical considerations behind the block copolymer self-assembly in solution and in the melt. The second part provides case studies of self-assembly in different classes of block copolymers (e.g., polyethers, polyelectrolytes) and in different environments (e.g., in water, in non-aqueous solvents, or in the absence of solvents). The third part presents experimental tools, ranging from static (e.g., small angle neutron scattering) to dynamic (e.g., rheology), which can prove valuable in the characterization of block copolymer self-assemblies. The fourth part offers a sampling of current applications of block copolymers in, e.g., formulations, pharmaceutics, and separations, applications which are based on the unique self-assembly properties of block copolymers.

Book American Doctoral Dissertations

Download or read book American Doctoral Dissertations written by and published by . This book was released on 1992 with total page 796 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Book Dissertation Abstracts International

Download or read book Dissertation Abstracts International written by and published by . This book was released on 1993-07 with total page 754 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Book Synthesis of Amphiphilic Block Copolymers and Their Interactions with Model Lipid Membranes

Download or read book Synthesis of Amphiphilic Block Copolymers and Their Interactions with Model Lipid Membranes written by and published by . This book was released on 2014 with total page 276 pages. Available in PDF, EPUB and Kindle. Book excerpt: Polymersome; Hybrid Lipid/Polymervesikel; Nanopartikel; Phasenseparation; Antikörperbindung; Diblockcopolymer; Triblockcopolymer; Polyisobutylen; Poly(ethylenoxid)

Book Synthesis and Characterization of Low Molecular Mass Amphiphilic Block Copolymers and Potential Use in Surfactant Assisted Particle Micro mixing

Download or read book Synthesis and Characterization of Low Molecular Mass Amphiphilic Block Copolymers and Potential Use in Surfactant Assisted Particle Micro mixing written by Ekaterini Karakatsanis and published by . This book was released on 2013 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt: In industry the effective mixing and de-agglomeration of two solid particles is vital in applications that require the intimate contact of homogeneously mixed reagents. One such application is in the preparation of pyrotechnic delay elements with reproducible burn speeds. The concept of surfactant assisted particle micro-mixing is proposed. This theory is based in the use of two amphiphilic polymeric surfactants to form two separate stable dispersions of the two solid particles to be mixed, but with the subsequent requirement that the dispersants are able to interact with each other. The formation of the individual dispersions allows for the deagglomeration of the particles and thus their preparation for homogeneous mixing, which is facilitated by the interacting surfactants. Low molecular mass block copolymers of styrene and acrylic acid and poly(ethylene oxide)-poly(propylene oxide) (PEO-PPO) surfactants are the proposed dispersants which will allow for the surfactant interaction by means of hydrogen bonding between the poly(acrylic acid) block and the PEO. The poly(styrene-co-acrylic acid) block copolymer will be synthesised via Atom Transfer Radical Polymerisation (ATRP) and subsequently used in the dispersion experiments. The synthesis of the polystyrene macroinitiators to initiate the block copolymerisation of the t-butyl acrylate was carried out satisfactorily, with good molecular masses and molecular mass distributions. In addition, lH-NMR analysis carried out on the polystyrene macroinitiators confirmed their synthesis. The use of the polystyrene macroinitiators was successful in synthesising poly(styrene-co-t-butyl acrylate) block copolymers with slightly higher polydispersities in comparison to the macroinitiatiators themselves, but acceptable. Hydrolysis of the poly(styrene-co-t-butyl acrylate) block copolymer to poly(styrene-co-acrylic acid) was successful in the presence of trifluoroacetic acid as catalyst. Attempts to hydrolyse in basic conditions (NaOH) and alternatively in acidic conditions (HCI) were not successful. Use of the poly(styrene-co-acrylic acid) amphiphilic block copolymer to emulsion polymerise styrene requires the ionised form of the polymer and was therefore not favourable to observe surfactant-surfactant hydrogen bonding. In addition, attempts to synthesise a wax emulsion stabilised by a PEO containing surfactant proved to be unsuccessful. Subsequently, the micro-mixing experiments were carried out by using a poly(acrylic acid) stabilised melamine dispersion and a commercially available PEO containing surfactant stabilised wax emulsion. The interaction between the melamine and the poly(acrylic acid) allows for the formation of a stable melamine dispersion at above 7% poly(acrylic acid) : melamine ratio (mass basis). Analysis by SEM shows that without the poly(acrylic acid) dispersant no wax particles are found to occur on the melamine particle surface. However, in an attempt to determine whether the amount of wax interaction increases with poly(acrylic acid) content, it was found that in the absence of poly(acrylic acid) dispersant, the most amount of wax precipitated out with the melamine. This is possibly attributable to the preferential occlusion of the wax particles between the melamine particles rather than surface attachment. Introduction of the poly(acrylic acid), however, shows via SEM analysis that the hydrogen bond interaction between the acrylic acid group and the ethylene oxide group does occur, since the attachment of the wax particles on the melamine particle surface is observed. Although results show that the surfactant-surfactant interaction allows for the micro mixing of particles, some refinement is required with respect to the systems that this phenomenon can be applied to. In addition, factors such as particle type, particle size and surfactant type will influence the micro-mixing interaction. It is therefore recommended that these factors be investigated in order to completely identify the micro-mixing phenomenon.

Book Synthesis of Reactive Amphiphilic Copolymers  Polymer Nanoparticles and Microgels Based on Oligoglycidol Macromonomers

Download or read book Synthesis of Reactive Amphiphilic Copolymers Polymer Nanoparticles and Microgels Based on Oligoglycidol Macromonomers written by Sascha Patrick Pargen and published by . This book was released on 2013-03 with total page 170 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Book Chemistry and Technology of Emulsion Polymerisation

Download or read book Chemistry and Technology of Emulsion Polymerisation written by A. M. van Herk and published by John Wiley & Sons. This book was released on 2008-04-15 with total page 328 pages. Available in PDF, EPUB and Kindle. Book excerpt: Emulsion polymerisation produces high value polymers in a low cost, environmentally friendly process. The drive to develop environmentally benign production methods for polymers has resulted in widespread development and implementation of the emulsion polymerisation technique. In addition, when combined with novel polymerisation mechanisms the process can give rise to a range of polymer products with particularly useful properties. Emulsion polymerisation is a complex process, governed by the interplay of both chemical and physical properties including polymerisation kinetics and dispersion stability. Successful industrial application relies on understanding and controlling those properties. By carefully explaining the principles of the reaction, based on well-designed experimental investigation, Chemistry and Technology of Emulsion Polymerisation provides a practical and intuitive explanation of emulsion polymerisation. In the development of industrial processes, coupling that understanding with everyday practice can be a further difficult step, so the book emphasises a clear, comprehensive and straightforward discussion to illustrate how the principles relate to practical application. Written for research chemists, technologists and engineers in the polymer, fine and specialty chemicals industries, and in university or government laboratories, this book will be particularly valuable to those early on in their careers. The comprehensive and straightforward coverage will also ensure it is an important resource for advanced courses in emulsion polymerisation.

Book Synthesis  Characterization and Self assembly of Amphiphilic Block Copolymers

Download or read book Synthesis Characterization and Self assembly of Amphiphilic Block Copolymers written by Xiaojun Wang and published by . This book was released on 2012 with total page 250 pages. Available in PDF, EPUB and Kindle. Book excerpt: This dissertation presents a review on state-of-the-art research of well-defined charged block copolymers, including synthesis, characterization, bulk morphology and self-assembly in aqueous solution of amphiphilic block polyelectrolytes. In Chapter 1, as a general introduction, experimental observations and theoretical calculations devoted towards understanding morphological behavior in charged block copolymer systems are reviewed along with some of the new emerging research directions. Further investigation of charged systems is urged in order to fully understand their morphological behavior and to directly target structures for the tremendous potential in technological applications. Following this background, in Chapters 2, 3, 4 and 5 are presented the design and synthesis of a series of well-defined block copolymers composed of charged and neutral block copolymers with full characterization: sulfonated polystyrene-b-fluorinated polyisoprene (sPS-b-fPI) and polystyrene-b-sulfonated poly(1,3-cyclohexadiene) (PS-b-sPCHD). Their bulk morphological behaviors in melts and self-assembly of sPS-b-fPI, PS-b-sPCHD in water were investigated. Some unique behaviors of sPS-b-fPI were discovered. The mechanisms for formation of novel nanostructures in aqueous solution are discussed in details in Chapter 4. Spherical and vesicular structures were formed from strong electrolyte block copolymers, e.g. PS-bsPCHD. Detailed light scattering and transmission electron microscopy were applied to characterize these structures. The abnormal formation of vesicles as well as microstructure effects on self-assembly is discussed in Chapter 5. In Chapter 6, we describe the successful synthesis of a well-defined acid-based block copolymers containing polyisoprene while maintaining the integrity of the functionality (double bonds) of polyisoprene. A general purification method is also presented in order to remove homo polyisoprene, polystyrene, and PS-b-PI in the di-, and tri-block copolymers. The self-assembly of PS-b-PI-b-PAA triblock terpolymers was studied in order to form multicompartmental structures in aqueous environments. In the last Chapter 7, detailed synthesis and characterization of a novel conjugate: poly(L-leucine) grafted hyaluronan (HA) (HA-g-PLeu) are presented. This work describes a new method to synthesize HA-g-PLeu via a "grafting onto" strategy. Due to the amphiphilic nature of this graft copolymers, a "local network" formed by self-assembly which was characterized by atomic force microscopy and light scattering. The secondary structure of the polypeptide was revealed by circular dichroism.

Book Amphiphilic Block Copolymers

Download or read book Amphiphilic Block Copolymers written by Tiambo Liu and published by . This book was released on 1999 with total page 888 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Book Synthesis and Self assembly of Multiple Thermoresponsive Amphiphilic Block Copolymers

Download or read book Synthesis and Self assembly of Multiple Thermoresponsive Amphiphilic Block Copolymers written by Jan Weiss and published by . This book was released on 2011 with total page 157 pages. Available in PDF, EPUB and Kindle. Book excerpt: In the present thesis, the self-assembly of multi thermoresponsive block copolymers in dilute aqueous solution was investigated by a combination of turbidimetry, dynamic light scattering, TEM measurements, NMR as well as fluorescence spectroscopy. The successive conversion of such block copolymers from a hydrophilic into a hydrophobic state includes intermediate amphiphilic states with a variable hydrophilic-to-lipophilic balance. As a result, the self-organization is not following an all-or-none principle but a multistep aggregation in dilute solution was observed. The synthesis of double thermoresponsive diblock copolymers as well as triple thermoresponsive triblock copolymers was realized using twofold-TMS labeled RAFT agents which provide direct information about the average molar mass as well as residual end group functionality from a routine proton NMR spectrum. First a set of double thermosensitive diblock copolymers poly(N-n-propylacrylamide)-b-poly(N-ethylacrylamide) was synthesized which differed only in the relative size of the two blocks. Depending on the relative block lengths, different aggregation pathways were found. Furthermore, the complementary TMS-labeled end groups served as NMR-probes for the self-assembly of these diblock copolymers in dilute solution. Reversible, temperature sensitive peak splitting of the TMS-signals in NMR spectroscopy was indicative for the formation of mixed star-/flower-like micelles in some cases. Moreover, triple thermoresponsive triblock copolymers from poly(N-n-propylacrylamide) (A), poly(methoxydiethylene glycol acrylate) (B) and poly(N-ethylacrylamide) (C) were obtained from sequential RAFT polymerization in all possible block sequences (ABC, BAC, ACB). Their self-organization behavior in dilute aqueous solution was found to be rather complex and dependent on the positioning of the different blocks within the terpolymers. Especially the localization of the low-LCST block (A) had a large influence on the aggregation behavior. Above the first cloud point, aggregates were only observed when the A block was located at one terminus. Once placed in the middle, unimolecular micelles were observed which showed aggregation only above the second phase transition temperature of the B block. Carrier abilities of such triple thermosensitive triblock copolymers tested in fluorescence spectroscopy, using the solvatochromic dye Nile Red, suggested that the hydrophobic probe is less efficiently incorporated by the polymer with the BAC sequence as compared to ABC or ACB polymers above the first phase transition temperature. In addition, due to the problem of increasing loss of end group functionality during the subsequent polymerization steps, a novel concept for the one-step synthesis of multi thermoresponsive block copolymers was developed. This allowed to synthesize double thermoresponsive di- and triblock copolymers in a single polymerization step. The copolymerization of different N-substituted maleimides with a thermosensitive styrene derivative (4-vinylbenzyl methoxytetrakis(oxyethylene) ether) led to alternating copolymers with variable LCST. Consequently, an excess of this styrene-based monomer allowed the synthesis of double thermoresponsive tapered block copolymers in a single polymerization step.

Book The Synthesis and Characterization of Amphiphilic Poly ethylene Oxide  block poly octadecyl Acrylate  Block Copolymers

Download or read book The Synthesis and Characterization of Amphiphilic Poly ethylene Oxide block poly octadecyl Acrylate Block Copolymers written by Yi Wang (Polymer engineer) and published by . This book was released on 2014 with total page 0 pages. Available in PDF, EPUB and Kindle. Book excerpt: A series of well-defined poly(ethylene oxide)-block-poly(octadecyl acrylate) (PEO-b-PODA) diblock copolymers were successfully synthesized by reversible addition fragmentation transfer (RAFT) polymerization with low polydispersities (M[subscript w]/M[subscript n] = 1.09-1.13). The crystallization behavior of poly(ethylene oxide)-block-poly(octadecyl acrylate) (PEO-b-PODA) diblock copolymers has been studied by differential scanning calorimetry (DSC), small-angle X-ray scattering (SAXS) and polarized optical microscopy (POM). The melt morphology of PEO455-PODA19 experienced a transition from lamella to cylinder at 130°C. For the double crystalline block copolymer PEO455-PODA19, the micro-phase separation at 55°C created lamellar micro-domains, which confined the PEO blocks as it crystallized. The leading crystallization of PEO blocks then created a space that confined PODA crystallites as they are developed. The spherulites were formed first when PEO started to crystallize, but crystallites with polyhedral shape finally formed. As for the micelle behavior, the transmission electron microscopy (TEM) showed that amphiphilic block copolymers PEO-PODA with different volume fractions of hydrophobic PODA blocks ranging from 21% to 54%, were able to self-assemble in water forming spherical micelles.

Book Synthesis and Characterization of Novel Polyisobutylene based Materials

Download or read book Synthesis and Characterization of Novel Polyisobutylene based Materials written by Lisa Kay Kemp and published by . This book was released on 2007 with total page 406 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Book Synthesis and Characterization of Well defined  Amphiphilic  Ionic Copolymers

Download or read book Synthesis and Characterization of Well defined Amphiphilic Ionic Copolymers written by Yuqing Liu (Polymer engineer) and published by . This book was released on 2011 with total page 208 pages. Available in PDF, EPUB and Kindle. Book excerpt: Amphiphilic ionic block copolymers are promising materials for the fabrication of ion-exchange membranes in fuel cells, water purification and advanced molecular engineering applications, such as nanotemplating. For example, block copolymer architectures provide a route to fabricate membranes with tunable transport properties through polymer self assembly. A significant challenge in this field is the synthesis of amphiphilic copolymers, where the intrinsic immiscibility of the hydrophobic and hydrophilic monomers complicates polymerization. To address the immiscibility between sodium p-styrenesulfonate and styrene monomers, styrenesulfonate monomers were neutralized by hydrophobic trialkyl ammonium salts via ion-exchange reactions, and synthesized successfully by RAFT polymerization with low polydispersity (PDI). Diblock or triblock copolymers with well-defined architectures were obtained by sequential RAFT polymerization with styrene. These sulfonate groups were then converted to the sodium salt form via ion-exchange to obtain amphiphilic ionic block copolymers. It was observed that dimethyl n-alkyl ammonium salts of polystyrenesulfonate displayed thermo-reversible gelation behavior in low polarity organic solvents. The investigation of the gelation behavior as a function of temperature, concentration, and solvent was consistent with gelation driven by the ionic aggregation of the polymer as would be expected for polyelectrolyte surfactant complexes in non-polar solvents. Cationic amphiphilic block/graft copolymers containing quaternary ammonium salts were prepared by the RAFT polymerization of polystyrene-b-poly(vinylbenzyl chloride) (PS-b-PVBC) copolymers, and sequential post-polymerization quaternization of the PVBC blocks. PS-b-PVBEA-b-PS triblock copolymers with well-defined architectures were obtained and the ion conductivity of the corresponding membranes, as well as the morphology of the membranes, was investigated. To improve the mechanical properties of the membranes, different architectures, such as pentablock, heptablock and graft copolymers, were designed and synthesized by RAFT polymerization, and chemical crosslinking was employed to improve the mechanical properties and control the swelling in water. Lastly, a new method to prepare multiblock copolymers via a facile route was developed. Polytrithiocarbonates were prepared by condensation polymerization of a dicarboxylic acid functional trithiocarbonate and a diol, and the trithiocarbonate group was controlled by tuning the amount of acid catalyst and reaction time. The polytrithiocarbonate RAFT agents were used to polymerize PS, polystyrene-b-poly (tert-butylstyrene) (PS-b-PtBS), and PS-b-PVBC. The PDI of the polymers toward 2, but the PDI of the polymer blocks between two trithiocarbonate groups was narrow (1.1-1.3 for PS and PS-b-PtBS, and 1.46 for PS-b-PVBC). The PVBC segments were quaternized to achieve anionic amphiphilic multiblock copolymers.