Search results for "Copolymer"

Glycidyl methacrylate derivatization of α,β-poly(N-hydroxyethyl)-dl-aspartamide and α,β-polyasparthydrazide

1997

Abstract α,β-Poly(N-hydroxyethyl)- dl -aspartamide (PHEA) and α,β-polyasparthydrazide (PAHy) are two synthetic macromolecules having many potential applications in the field of biomedical sciences. This paper describes the functionalization of PHEA and PAHy with glycidyl methacrylate (GMA), in order to introduce pendant double bonds in their chains. Derivatized PHEA and PAHy (samples PHG and PAG, respectively) at various GMA content have been obtained and characterized. It has been shown that the derivatization reaction can be controlled by varying some parameters as solvent, catalyst, pH, GMA concentration and reaction time. As expected, PAHy reacted more rapidly and more extensively than …

1991

Tracer diffusion coefficients D* of both components were measured in mixtures of polystyrene (PS) and polymethylstyrene (PMS), a random copolymer from 60 wt.-% of m-methylstyrene and 40 wt.-% of p-methylstyrene. The results are interpreted in terms of the free-volume theory which yields master curves even for “asymmetric” mixtures of oligomer and polymer chains, if D* is drawn versus the distance from the glass transition temperature, T–Tg. Whereas D* was measured by the forced Rayleigh scattering technique, we also studied photon correlation spectroscopy in these mixtures and observed “slow modes” with decay constants that correspond to diffusion coefficients 2–3 decades smaller than the i…

Amphiphilic Polyethers of Controlled Chain Architecture

2003

The amphiphilic polymers, polymers which contain in their macromolecules both hydrophilic and hydrophobic units1, are the base for valuable materials due to their diversified interaction with liquids. So they may act as emulsifiers, compatibilizers, “smart” materials (responding to external stimuli)2 and many others. In order to control their properties, the hydrophilic — hydrophobic balance in the macromolecules has to be controlled. This balance depends not only upon the constitution of the chain repeating units, but also upon the art of their distribution in the chains (copolymers of controlled unit sequences), the chain topology, the size of the chains and many others. So a careful engi…

Kinetics and Mechanisms in the Anionic Polymerization of Methacrylic Esters

1987

Under appropriate conditions the anionic polymerization of methacrylates proceeds in an ideal manner leading to polymers with narrow molecular weight distributions. From the kinetics of polymerization and from the microstructure of the polymers the existence of different active species is concluded, the most important one being a peripherally solvated contact ion pair. Depending on polymerization conditions two different modes of monomer addition can occur. Homo- and copolymerization experiments show that the influence of the ester group is mainly given by electronic effects. In non- polar solvents the polymerization of tert.-butyl methacrylate (in contrast to methyl methacrylate) leads to …

Copolymers sensitive to temperature and pH in water and in water+oil mixtures: A DSC, ITC and volumetric study

2011

Block copolymer micelles are receiving an increasing interest because of the variety of structures and the possibilities to tune them by changing external and internal parameters achieving the desired properties for a specific purpose. We have investigated the acid/base behavior, self-assembling and solubilization ability towards polar oils of star-like copolymers named Tetronics. They are composed of branched four-arms each one consisting of two blocks made of EO and PO units linked to the diethylenediamine group, which confers pH response ability. The copolymers T1107 and T90R4 were studied with a sequential and reverse architecture. The thermodynamics of the acid/base equilibrium was stu…

Rod-Length Dependent Aggregation in a Series of Oligo(p-benzamide)-Block-Poly(ethylene glycol) Rod-Coil Copolymers

2005

The synthesis of a series of rod-coil diblock copolymers with flexible poly(ethylene oxide) chains (M n = 5 000 g mol -1 ) and rod blocks consisting of monodisperse oligo(p-benzamide)s is described. The formation of defined supramolecular aggregates in solution as well as the solid state has been analyzed. The length of the oligo(p-benzamide)s has been systematically varied from n = 1 to 7 units. The influence of n on aggregation in chloroform and aqueous solution was investigated by GPC as well as UV-vis spectroscopy. A critical aggregation length was found for chloroform (n = 5) and water (n = 4), below which no aggregation is observed under otherwise identical experimental conditions. Ag…

Temperature-responsive inclusion complex of cationic PNIPAAM diblock copolymer and γ-cyclodextrin

2012

Aqueous mixtures of γ-cyclodextrin (γ-CD) and the thermosensitive cationic diblock copolymer poly(N-isopropylacrylamide)-b-poly(3-acrylamidopropyl)trimethylammonium chloride (PNIPAAM24-b-PAMPTAM(+)9) or the PNIPAAM homopolymer PNIPAAM47 have been investigated using various experimental methods. Solid γ-CD–polymer inclusion complexes (pseudopolyrotaxanes) form at ambient temperatures in fairly concentrated CD solutions. The NMR measurements showed that the stoichiometry of the inclusion complexes is close to two NIPAAM units per CD molecule. The cationic block of the copolymer is not incorporated into the CD cavity. Synchrotron radiation X-ray diffraction spectra of the solid inclusion compl…

Adsorption of triblock copolymers and their homopolymers at laponite clay/solution interface. Role played by the copolymer nature

2009

The adsorption thermodynamics of copolymers, based on ethylene oxide (EO) and propylene oxide ( PO) units, at the laponite (RD) clay/liquid interface was determined at 298 K. The copolymer nature was tuned at molecular level by changing the hydrophilicity, the architecture and the molecular weight (Mw) keeping constant the EO/PO ratio. Polyethylene (PEGs) and polypropylene (PPGs) glycols with varying Mw and their mixture were also investigated to discriminate the role of the EO and the PO segments in the adsorption process. Enthalpies of transfer of RD, at fixed concentration, from water to the aqueous macromolecule solutions as functions of the macromolecule molality were determined. They …

Kinetic studies of the interaction between DNA and polycations based on polyasparthylhydrazide

2008

Abstract In the present paper, a systematic kinetic study on the interaction between interpolyelectrolytes such as positive-charged polymers and DNA was carried out. In particular, a qualitative–quantitative kinetic investigation on the interaction between copolymers of the α,β-poly(aspartylhydrazide) and DNA calf thymus filaments was performed. This study gives a new model starting from a well known “pseudo-phase model”, and permits to give a qualitative explanation about the trends of experimentally observed kinetic constants by varying the concentration of one of the two poly-electrolytes. Moreover, this study permits to verify the dependence of the binding constants KPAHy–CPTA and KDNA …

A Facile Approach for Transferring Hydrophobic Magnetic Nanoparticles into Water-Soluble Particles

2008

A novel, easy and high-efficient method is described for transferring hydrophobic magnetic Fe 3 O 4 nanoparticles from organic to aqueous solution by wrapping a thermo-responsive and photocrosslinkable poly(N-isopropylacrylamide) (PNIPAm) terpolymer around the particles. The wrapping procedure is introduced by the co-nonsolvent transition of PNIPAm in the mixing solvent and the polymer can dissolve in water carrying Fe 3 O 4 nanoparticles by noncovalent interaction. The temperature-dependant and magnetic properties of the water-soluble particles are characterized in this paper.