Investigation of the General Properties of Some Polyelectrolyte Complexes

Investigation of the General Properties of Some Polyelectrolyte Complexes PDF Author: Nermin Acar
Publisher:
ISBN:
Category :
Languages : en
Pages :

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Book Description
Polyelectrolyte complexes, also called interpolymer complexes, are new class of chemically distinct and identifiable compounds. They are formed by polyelectrolytes that are macromolecules carrying a relatively large number of functional groups, orunder suitable conditions can become charged. Polyelectrolytes interact with various low and high molecular weight substances and form interpolymer complexes. These complexes are either separated from the solution as solids (polycomplex salt) or may settle as a polyelectrolyte complex gel, and they can be soluble in solution by controlling experimental factors. They are, in general, obtained in either case, by mixing polyelectrolytes solution, and by matrix polymerization. Significant differences might exist between the chemical, thermal and mechanical properties ofinterpolymer complexes with respect to their components and experimental conditions. All biological macromolecules, proteins, nucleic acids, and polysaccharides are polyelectrolytes and interact with each other and small ions during their biological function. Their electrostatic interactions contribute a significant part of the structural stabilization of biological molecules and they are major determinants for the kinetics of biological process. Considering all these vital processes research on the polyelectrolyte complexes obtained by synthetic polyelectrolytes might be a simple model system for the complicated biopolymer reactions. Studying the special properties of polycomplex formation between synthetic polyelectrolytes and low molecular weight compounds can be useful for understanding the nature of protein-lipid interaction in biomembranes or in the mechanism of protein denaturation. On the other hand, polyelectrolyte complexes are very promising materials for semi-permeable membranes for the industrial applications such as desalting of sea water, ultrafiltration and purification of aqueous solution and also for ultrafiltration of biological liquids.With all the above given respects, numerous studies have been made successively onvarious polyelectrolyte complexes in the last two decades. However very few studies have been reported on the interaction between some certain polyphosphates andvinylpyridine polymers. One of a few studies with poly(phosphate) has been given by N.Acar and T.Tulun on the interaction of poly(sodiumphosphate) (PSP) andpoly(4-vinylpyridiniumchloride) (P4VPHCl). The present study was aimed to investigate the interaction between poly(sodiumphosphate) and poly(4-vinylpyridiniumchloride) with 4-amino benzoic acid (low molecular weight compound) individually as well as the detailed continuation of the previous work which dealt with the polyelectrolyte complex formed by PSP and P4VPHCl.Poly(sodium phosphate) is interesting because it is an inorganic polymer and, rather unusually it is one of the few anionic polymers of the integral type. Actually polyphosphates are somewhat analogous to the nucleic acids. Vinylpyridine polymers have particular importance as polyelectrolytes and have great ability to develop interpolymer complexes with polyacids.The present study aims to form polyelectrolyte model complexes similar to or mimicking biologically active compounds and, thus, to understand the operating mechanism of biopolymers in living organisms through the investigation of the structure and various features of these model complexes. In the experimental part of the study, insoluble polyelectrolyte complexes were obtained from the both, concentrated and dilute solutions of PSP and P4VPHCl. Stoichiometry of the isolated complexes were found to be 1:1 as a result of analysis of the supernatant liquid in conjunction with concentration of the initial components.In the dilute aqueous solution, occurrence of polyelectrolyte complex was proved by UV spectroscopy. Salt effect of NaCl, the effect of NaCl on complex formation andthermal properties of complexes were investigated.Regarding the reaction of PSP with 4-amino benzoic acid, hydrochloride (PABCl),the stoichiometry of complex was found as 1:1.2 using viscometric and volumetricanalysis of the supernatant. Besides, spectroscopic and conductometric methods were used for the complex stoichiometry. The experimental factors such as pH,ionic strength and temperature that affect the stoichiometry of complex were investigated.In the case of the poly(4-vinylpyridine) (P4VP) with 4-aminobenzoic acid, IR spectroscopy , potentiometry and DSC were used and the nature of binding between the components was identified as hydrogen bonding.It is known that transition metals take part in the biochemical process. In the present study, interaction of copper (II) with P4VP- PABA complex system is of interest. Potentiometric method was used to follow the above stated interaction in aqueousethanol solution for P4VP-PABA system. Protonation and the stability constants ofP4VP-PABA system were determined.Swelling properties of polyelectrolyte systems have been studied largely due to their industrial uses. In order to investigate the swelling properties of P4VPHCl-PSP system, PSP and P4VP that is the initial component of polycation were subjected to irradiation for six different radiation doses to obtain cross linked structure. It is found that radiation has no affect on PSP.After irradiation the insoluble, the gel, parts were determined by soxhlet extraction and UV spectroscopy. Up to certain dose the gelpercent of P4VP samples increased, and thereafter remained unchanged. From the relation between gel fraction and radiation dose, the efficiency of crosslinking and of scission were determined. Irradiated P4VP that contained only gel part was quaternized to obtain waterswellable P4VPHCl gel. The interaction of P4VPHCl gel with the aqueous solution of PSP was investigated considering ionic strength and pH.

Investigation of the General Properties of Some Polyelectrolyte Complexes

Investigation of the General Properties of Some Polyelectrolyte Complexes PDF Author: Nermin Acar
Publisher:
ISBN:
Category :
Languages : en
Pages :

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Book Description
Polyelectrolyte complexes, also called interpolymer complexes, are new class of chemically distinct and identifiable compounds. They are formed by polyelectrolytes that are macromolecules carrying a relatively large number of functional groups, orunder suitable conditions can become charged. Polyelectrolytes interact with various low and high molecular weight substances and form interpolymer complexes. These complexes are either separated from the solution as solids (polycomplex salt) or may settle as a polyelectrolyte complex gel, and they can be soluble in solution by controlling experimental factors. They are, in general, obtained in either case, by mixing polyelectrolytes solution, and by matrix polymerization. Significant differences might exist between the chemical, thermal and mechanical properties ofinterpolymer complexes with respect to their components and experimental conditions. All biological macromolecules, proteins, nucleic acids, and polysaccharides are polyelectrolytes and interact with each other and small ions during their biological function. Their electrostatic interactions contribute a significant part of the structural stabilization of biological molecules and they are major determinants for the kinetics of biological process. Considering all these vital processes research on the polyelectrolyte complexes obtained by synthetic polyelectrolytes might be a simple model system for the complicated biopolymer reactions. Studying the special properties of polycomplex formation between synthetic polyelectrolytes and low molecular weight compounds can be useful for understanding the nature of protein-lipid interaction in biomembranes or in the mechanism of protein denaturation. On the other hand, polyelectrolyte complexes are very promising materials for semi-permeable membranes for the industrial applications such as desalting of sea water, ultrafiltration and purification of aqueous solution and also for ultrafiltration of biological liquids.With all the above given respects, numerous studies have been made successively onvarious polyelectrolyte complexes in the last two decades. However very few studies have been reported on the interaction between some certain polyphosphates andvinylpyridine polymers. One of a few studies with poly(phosphate) has been given by N.Acar and T.Tulun on the interaction of poly(sodiumphosphate) (PSP) andpoly(4-vinylpyridiniumchloride) (P4VPHCl). The present study was aimed to investigate the interaction between poly(sodiumphosphate) and poly(4-vinylpyridiniumchloride) with 4-amino benzoic acid (low molecular weight compound) individually as well as the detailed continuation of the previous work which dealt with the polyelectrolyte complex formed by PSP and P4VPHCl.Poly(sodium phosphate) is interesting because it is an inorganic polymer and, rather unusually it is one of the few anionic polymers of the integral type. Actually polyphosphates are somewhat analogous to the nucleic acids. Vinylpyridine polymers have particular importance as polyelectrolytes and have great ability to develop interpolymer complexes with polyacids.The present study aims to form polyelectrolyte model complexes similar to or mimicking biologically active compounds and, thus, to understand the operating mechanism of biopolymers in living organisms through the investigation of the structure and various features of these model complexes. In the experimental part of the study, insoluble polyelectrolyte complexes were obtained from the both, concentrated and dilute solutions of PSP and P4VPHCl. Stoichiometry of the isolated complexes were found to be 1:1 as a result of analysis of the supernatant liquid in conjunction with concentration of the initial components.In the dilute aqueous solution, occurrence of polyelectrolyte complex was proved by UV spectroscopy. Salt effect of NaCl, the effect of NaCl on complex formation andthermal properties of complexes were investigated.Regarding the reaction of PSP with 4-amino benzoic acid, hydrochloride (PABCl),the stoichiometry of complex was found as 1:1.2 using viscometric and volumetricanalysis of the supernatant. Besides, spectroscopic and conductometric methods were used for the complex stoichiometry. The experimental factors such as pH,ionic strength and temperature that affect the stoichiometry of complex were investigated.In the case of the poly(4-vinylpyridine) (P4VP) with 4-aminobenzoic acid, IR spectroscopy , potentiometry and DSC were used and the nature of binding between the components was identified as hydrogen bonding.It is known that transition metals take part in the biochemical process. In the present study, interaction of copper (II) with P4VP- PABA complex system is of interest. Potentiometric method was used to follow the above stated interaction in aqueousethanol solution for P4VP-PABA system. Protonation and the stability constants ofP4VP-PABA system were determined.Swelling properties of polyelectrolyte systems have been studied largely due to their industrial uses. In order to investigate the swelling properties of P4VPHCl-PSP system, PSP and P4VP that is the initial component of polycation were subjected to irradiation for six different radiation doses to obtain cross linked structure. It is found that radiation has no affect on PSP.After irradiation the insoluble, the gel, parts were determined by soxhlet extraction and UV spectroscopy. Up to certain dose the gelpercent of P4VP samples increased, and thereafter remained unchanged. From the relation between gel fraction and radiation dose, the efficiency of crosslinking and of scission were determined. Irradiated P4VP that contained only gel part was quaternized to obtain waterswellable P4VPHCl gel. The interaction of P4VPHCl gel with the aqueous solution of PSP was investigated considering ionic strength and pH.

Compositions and Viscoelastic Properties in Solid Polyelectrolyte Complexes

Compositions and Viscoelastic Properties in Solid Polyelectrolyte Complexes PDF Author: Yuhui Chen
Publisher:
ISBN:
Category : Chemistry
Languages : en
Pages : 0

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Book Description
Polyelectrolytes are polymers bearing charged repeat units. Based on the charge, a polyelectrolyte can be categorized as either a polycation or a polyanion. When dissolved in water, the charges on a polyelectrolyte are balanced by small counterions. Mixing certain polycations and polyanions in an aqueous solution will result in solid precipitants due to polymer-polymer interactions and the entropy gain of releasing the small counterions. This type of material is called polyelectrolyte complexes, PECs. PECs have a wide range of applications including drug delivery systems, film coatings, and membranes. Because of their charged nature, PECs can bind with enzymes and DNA or many bio-medical applications. To further explore the applications of PECs, it is important to understand the dynamics and viscoelastic properties of this special type of polymer. Many factors such as water, temperature, and composition heavily influence the behaviors of PECs, and therefore were studied in this work.The first part of the dissertation focuses on water and the viscoelastic properties of various PECs. Thirteen different polyelectrolytes were used to produce those PECs, and radiolabeling and NMR techniques were used to determine the polycation: polyanion stoichiometry in the materials. Rheological studies were performed on those PECs to determine their glass transition temperatures, Tg. The PECs exhibit a wide range of Tgs within the working range of aqueous solutions between 0 and 100 °C. To study the correlation between Tg and water, a radiochemical method was developed to measure the pore volume within the PECs, which was used to differentiate between PEC water and pore water. Contrary to what was generally believed, the Tg correlated poorly with the water volume fraction in PECs. There was a weak correlation in a series of PECs in which one of the polyelectrolytes was held constant. On the other hand, time-temperature superposition of linear viscoelastic responses provided a classical estimate of the fractional free volume of PECs, which correlated well with Tg. The second part investigated the correlation between the stoichiometry and viscoelastic properties of a certain PEC, poly(diallydimethylammonium) (PDADMA)/poly(4-styrenesulfonic acid) (PSS). Various nonstoichiometric PECs with excess in either PDADMA or PSS were produced by a "quenching" method. A xvi maximum of 36% molar excess of PDADMA or 40% molar excess of PSS was achieved. Those nonstoichiometric PECs exhibited lower Tgs compared to stoichiometric ones, and an excess of PDADMA had a bigger effect on lowering the Tg. It was shown that the decrease in Tg was caused by the increase in water content. Due to the excess polyelectrolytes and counterions, more water was introduced to the nonstoichiometric PECs and therefore lowered the Tg via the plasticizing effect. In addition, time-temperature superposition revealed a correlation between segmental relaxation times and stoichiometry. Nonstoichiometric PECs were shown to have elevated fractional free volumes and decreased polymer volume fractions, which are responsible for changes in their mechanical properties. The third part focuses on the formation and properties of PEC blends. Four PECs with distinct Tgs were used to produce two PEC blends with varying compositions. Each blend is comprised of one polycation and two polyanions, and the molar ratio of the two polyanions was adjusted to create blends with the same components but different molar compositions. Rheological experiments were carried out to determine the Tgs of the blends. It was shown that one of the blends exhibited Tgs in between the two individual PECs, and the Tgs can be modeled using the Kwei Equation. The other blend showed two different Tgs that were similar to the individual PECs' Tgs, indicating the blend was immiscible. The immiscibility was explained by the difference in critical salt concentration between the two individual PECs.

Physical Chemistry of Polyelectrolytes

Physical Chemistry of Polyelectrolytes PDF Author: Tsetska Radeva
Publisher: CRC Press
ISBN: 1482270684
Category : Science
Languages : en
Pages : 936

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Book Description
An examination of the fundamental nature of polyelectrolytes, static and dynamic properties of salt-free and salt-added solutions, and interactions with other charged and neutral species at interfaces with applications to industry and medicine. It applies the Metropolis Monte Carlo simulation to calculate counterion distributions, electric potentia

Polyelectrolytes

Polyelectrolytes PDF Author: Visakh P. M.
Publisher: Springer
ISBN: 3319016806
Category : Technology & Engineering
Languages : en
Pages : 388

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Book Description
This book offers a valuable reference source to graduate and post graduate students, engineering students, research scholars polymer engineers from industry. The book provides the reader with current developments of theoretical models describing the thermodynamics polyelectrolytes as well as experimental findings. A particular emphasis is put on the rheological description of polyelectrolyte solutions and hydrogels.

Physical Chemistry of Polyelectrolyte Solutions, Volume 158

Physical Chemistry of Polyelectrolyte Solutions, Volume 158 PDF Author: Mitsuru Nagasawa
Publisher: John Wiley & Sons
ISBN: 1119057086
Category : Science
Languages : en
Pages : 298

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Book Description
The Advances in Chemical Physics series provides the chemical physics field with a forum for critical, authoritative evaluations of advances in every area of the discipline. This volume explores topics from Thermodynamic Properties of Polyelectrolyte Solutions to ion-binding of polyelectrolytes. The book features: The only series of volumes available that presents the cutting edge of research in chemical physics Contributions from experts in this field of research Representative cross-section of research that questions established thinking on chemical solutions An editorial framework that makes the book an excellent supplement to an advanced graduate class in physical chemistry or chemical physics

Effects of Solution Composition (salts, PH, Dielectric Constant) on Polyelectrolyte Complex (PEC) Formation and Their Properties

Effects of Solution Composition (salts, PH, Dielectric Constant) on Polyelectrolyte Complex (PEC) Formation and Their Properties PDF Author: Huan Zhang (Polymer engineer)
Publisher:
ISBN:
Category : Photoelectrochemistry
Languages : en
Pages : 0

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Book Description
Polyelectrolyte complexes (PECs) are formed based on the strong association of oppositely charged polyelectrolytes, a process driven by a combination of enthalpy and entropy, but often with entropic considerations dominating. PEC based materials including polyelectrolyte coacervates, precipitates, and multilayers (PEMs), exhibit promising application in a variety of areas. These abundant applications of PECs are made possible by their highly controllable/tailorable properties upon exposure to different stimuli like pH, salt, organic solvent, and so on. It is important to understand how these different parameters affect the complexation of polyelectrolytes and the structures of PECs. In this dissertation, the main goal is to investigate the effects of solution composition including salt content, pH of solution, and solvent quality on the properties of polyelectrolyte coacervate, precipitate and multilayers. Based on these studies, the potential of applications of PEC materials in self-healing, 3D printing under ethanol and adhesive were studied. Firstly, the interactions between various types of salt and polyelectrolytes were studied. The energetics of the binding process between salt and polyelectrolytes were investigated. Various types of cations and anions were employed in this study, including alkali metal, alkaline earth metal ions, transition metal ions and a Hofmeister series of anions. Based on the different interactions between these ions and polyelectrolytes, the salts present different effects on the properties of PECs. Salt effects on coacervate, especially coacervate stability, are summarized in Chapter III. Chapter IV shows the study of salt effects on the properties of PEMs including the growth and swelling/deswelling behaviors. In Chapter V, the effects of salt and pH on the self-healing ability of bulk PEC materials were studied. The rheological properties of hydrated, bulk PEC material are strongly influenced by salt and pH treatment, which directly controls the crosslink density in the material, chain mobility, and therefore self-healing ability. Alkali metal ions and transition metal ions show different effects on the self-healing ability of the BPEI/PAA complex. The effects of these two different types of salts on complex are reversible, which presents a possible way to control the material properties, ranging from self-healing to completely unable to do so. Due to changes in charge density of weak polyelectrolytes in response to pH, the self-healing of weak PECs can be enhanced by pH treatment as well. In Chapter VI, the effects of ethanol on the complexation of polyelectrolytes, rheological properties and structure of polyelectrolyte precipitates were investigated. The complexation of polyelectrolytes is inhibited by the presence of ethanol due to the weakening interactions between polycation and polyanion under low dielectric constant environment. For the polyelectrolyte precipitate formed from higher ethanol content mixture, the precipitate shows a smaller modulus and larger loss angle. In comparison, by immersing polyelectrolyte precipitate in a higher ethanol content mixture, the precipitate shows an increased modulus. This enhancement of mechanical properties is mainly due to the dehydration of the polyelectrolyte precipitate, which results in an enhanced interaction between BPEI and PAA (lowering the dielectric constant surrounding ion pairs strengthens them). The precipitate formed from high ethanol content mixture (vol% of ethanol > ~ 40%) can be dissolved in water to form a highly viscous polyelectrolyte coacervate, which shows potential applications in 3D printing under ethanol. In Chapter VII, electrophoretic deposition (EPD) was used to fabricate polyelectrolyte complex films, and it was shown to create thicker films than those created by the simple deposition of polyelectrolyte complexes in the absence of external electrical fields. A pulsed EPD with controlled pulse ON time and pulse OFF times can effectively suppress the formation of these bubbles. The mobility and zeta potential of BPEI/PAA complexes are modulated by the ratio of BPEI to PAA and pH of complexes, which will affect the thickness of deposited complex film. Regardless of different pulsed mode, by changing the electric field strength, the maximum thickness of BPEI/PAA complex film is obtained at a moderate electric field strength. High electric field strength will result in the dissolution of BPEI/PAA complexes due to formation of air bubbles and the high pH environment near the working electrode. In contrast, by using strong polyelectrolyte complex pair, PDAC/PSS, a proportional relationship between the thickness of complex film and electric field strength is observed. Therefore, the local pH change near working electrode is an important factor in the deposition of weak polyelectrolyte pairs. Moreover, ionic strength of the complex solution influences the charge density and stability of BPEI/PAA polyelectrolyte complexes. This work also shows the fabrication of polyelectrolyte complex-dye films using EPD. The loading of dye in complex films can be enhanced using proper EPD method.

Physics of Protein-polyelectrolyte Complexes

Physics of Protein-polyelectrolyte Complexes PDF Author: Rituparna Samanta
Publisher:
ISBN:
Category :
Languages : en
Pages : 0

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Book Description
A mixture of proteins and polyelectrolytes are widely used in applications such as food systems, biosensors, protein purification, drug delivery. Experiments have demonstrated that the structures and phase behavior of protein-polyelectrolyte mixture can be dependent on a variety of factors, including the physical and chemical characteristics of proteins, polyelectrolytes, properties of solution, and temperature. Despite extensive experimental studies, there is still a lack of a theoretical framework to understand the fundamental physics which is capable of capturing the complexities of the phase behavior of protein-polyelectrolyte mixtures and be able to predict the impact of the component properties on the structure of these mixtures. Motivated by the lack of studies, in this thesis, we have built a single chain in mean-field based coarse-grained multibody simulation framework to study the phase behavior of protein and polyelectrolyte complexes. We have explored the influence of features such as the dielectric difference between the protein and the solvent, charge distribution of proteins, and the solution pH. Our results demonstrate that the pattern of charge heterogeneities can exert a significant influence on the resulting characteristics of the aggregates, in some cases leading to a transformation from polymer-bridged complexes to direct protein aggregates driven by attraction between oppositely charged patches. Later, we appended the framework to capture the influence of variable charge on proteins and polyelectrolytes due to variation in their dissociation characteristics in the presence of other charged species and properties of the solution. We probe the influence of charge patches on the bridging probabilities near the protein isoelectric points and in regimes in which the net charge of the protein is the same sign as that of the polyelectrolytes. Our results demonstrate that in the presence of dissociable polyelectrolytes, the probability of bridging of proteins capable of charge regulation is enhanced relative to proteins which are completely dissociated. For homogeneously charged proteins and/or proteins with weak charge heterogeneities, partially dissociated polyelectrolytes are seen to exhibit enhanced bridging characteristics compared to completely dissociated polyelectrolytes. In contrast, for proteins exhibiting strong charge heterogeneities, dissociable polyelectrolytes are seen to exhibit weaker bridging compared to completely dissociated polyelectrolytes. Upon including the feature of dielectric contrast in the model, our results demonstrated that the proteins experienced an increased repulsion with a lowering of the ratio of protein to the solvent dielectric constant. However, the influence of dielectric contrast diminishes with an increase in the particle volume fraction and/or its charge. In the presence of neutral polymers, similar effects manifest, but with the additional physics arising from the fact that the polymer-induced interactions are influenced by the dielectric contrast of the protein and solvent. Finally, we designed a framework to capture the phase diagram of the protein

Polyampholytes

Polyampholytes PDF Author: Sarkyt E. Kudaibergenov
Publisher: Springer Science & Business Media
ISBN: 9780306467813
Category : Science
Languages : en
Pages : 232

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Book Description
This book comprehensively reviews the synthesis, characterization and application aspects of linear and crosslinked synthetic polyampholytes - simple model of biopolymers - starting from the 1950's. The synthetic strategy of "annealed", "quenched" and "zwitterionic" polyampholytes, the properties of polyampholytes in solutions and in gel state are considered. The complexation ability of polyampholytes with respect to transition metal ions, ionic surfactants, dyes and organic probes polyelectrolytes, proteins and colloid particles is discussed. Stimuli-sensitive behavior of various amphoteric gel and membrane systems demonstrating rhythmically phenomenon similar to that of heart beat, deformation, oscillation or self-oscillation phenomena stimulated by temperature, pH and electric field are illustrated. Catalytic properties of synthetic polyampholytes simulating the function of enzymes are also considered.

Adhesive Properties of Wet Polyelectrolyte Multilayer Films and Electrophoretic Deposition of Polyelectrolyte Complexes

Adhesive Properties of Wet Polyelectrolyte Multilayer Films and Electrophoretic Deposition of Polyelectrolyte Complexes PDF Author: Chao Li
Publisher:
ISBN:
Category : Polyelectrolytes
Languages : en
Pages : 82

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Book Description
Weak polyelectrolyte multilayers prepared by using layer-by-layer (LbL) technique are known to become sticky upon contact with water and behave as a viscoelastic fluid, but the full extent of this wet adhesive property is not fully understood. In this study, the wet adhesive performance of polyelectrolyte multilayers consisting of branched poly(ethylene imine) and poly(acrylic acid) under controlled conditions was investigated by using a 90° peel test. The peel force is highest under neutral condition, and it decreases in acidic/basic environment. The addition of metal ions changes the peel force, either increasing it or decreasing it based on the nature of the metal ion. Addition of Cu2+ stiffens multilayers, preventing multilayers from acting as an effective wet adhesive. The films are also characterized with zeta potential and shear rheometry, and the adhesiveness can be recovered by rewetting for at least 5 times. This polyelectrolyte based wet adhesive can be adhered to soft, wet surfaces like biological tissues such as liver. These multilayer films in this work show wet adhesive properties, however, the layer by layer technique used to fabricate these films requires several steps and take a long time. Therefore, new methods are needed to make these thin films. Spin-assisted LbL assembly, spray-assisted LbL assembly and electric field-assisted LbL assembly are widely studied because they are simple and time-saving. Electric field-assisted LbL assembly has been gaining an increasing interest. One option for realizing this may be the electrophoretic deposition of weak polyelectrolyte complexes, made by mixing polyelectrolytes of opposite charge together, has not been studied yet. Therefore, electrodeposition of polyelectrolyte complexes under different conditions (i.e. pH, ratio of polycation and polyanion, concentration of polyelectrolyte complexes, concentration of salt and type of electric field) was investigated in this work. Polyelectrolyte complexes at moderate pH values and at the ratio of polycation and polyanion at 20 shows highest electrophoretic mobility. The thickness of polyelectrolyte complex film decreases with decreasing the concentration of polyelectrolyte complexes while the thickness increases when a proper amount of salt is added during preparing polyelectrolyte complexes. Under controlling pulse current at 10mA, a thicker film can be achieved but the surface is rougher compared with one prepared by using pulse potential at 10V. This work provides insight into both the wet adhesive properties of polyelectrolyte multilayers and electrophoretic deposition of polyelectrolyte complexes.

High Performance Biomaterials

High Performance Biomaterials PDF Author: Michael Szycher
Publisher: Routledge
ISBN: 1351440950
Category : Technology & Engineering
Languages : en
Pages : 854

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Book Description
Encyclopedic presentation of the clinical applications of biomaterials from markets and advanced concepts to pharmaceutical applications and blood compatibility.