Search results for "copolymer"
showing 10 items of 1003 documents
PAA-PAMPS Copolymers as an Efficient Tool to Control CaCO3 Scale Formation
2013
Scale formation, the deposition of certain minerals such as CaCO3, MgCO3, and CaSO4 center dot 2H(2)O in industrial facilities and household devices, leads to reduced efficiency or severe damage. Therefore, incrustation is a major problem in everyday life. In recent years, double hydrophilic block copolymers (DHBCs) have been the focus of interest in academia with regard to their antiscaling potential. In this work, we synthesized well-defined blocklike PAA-PAMPS copolymers consisting of acrylic acid (AA) and 2-acrylamido-2-methyl-propane sulfonate (AMPS) units in a one-step reaction by RAFT polymerization. The derived copolymers had dispersities of 1.3 and below. The copolymers have then b…
An asymmetric electrospun membrane for the controlled release of ciprofloxacin and FGF-2: Evaluation of antimicrobial and chemoattractant properties.
2021
Here, an asymmetric double-layer membrane has been designed and fabricated by electrospinning as a tool for a potential wound healing application. A hydrophobic layer has been produced by using a polyurethane-polycaprolactone (PU-PCL) copolymer and loaded with the antibacterial ciprofloxacin whereas an ion responsive hydrophilic layer has been produced by using an octyl derivative of gellan gum (GG-C8) and polyvinyl alcohol (PVA) and loaded with the growth factor FGF-2. This study investigated how the properties of this asymmetric membrane loaded with actives, were influenced by the ionotropic crosslinking of the hydrophilic layer. In particular, the treatment in DPBS and the crosslinking i…
Rapid Production of Internally Structured Colloids by Flash Nanoprecipitation of Block Copolymer Blends.
2018
Colloids with internally structured geometries have shown great promise in applications ranging from biosensors to optics to drug delivery, where the internal particle structure is paramount to performance. The growing demand for such nanomaterials necessitates the development of a scalable processing platform for their production. Flash nanoprecipitation (FNP), a rapid and inherently scalable colloid precipitation technology, is used to prepare internally structured colloids from blends of block copolymers and homopolymers. As revealed by a combination of experiments and simulations, colloids prepared from different molecular weight diblock copolymers adopt either an ordered lamellar morph…
Pillar[5]arene-Diketopyrrolopyrrole Fluorescent Copolymer: A Promising Recognition and Adsorption Material for Adiponitrile by Selective Formation of…
2017
Conjugated pillar[5]arene-diketopyrrolopyrrole copolymer (P1) is synthesized by the copolymerization of a difunctionalized pillar[5]arene and a diketopyrrolopyrrole-based monomer, which shows large extinction coefficients (1.1 × 104 m-1 cm-1 ) at 519 nm and strong emission at 587 nm. P1 exhibits very strong host-guest binding affinity towards adiponitrile but low binding affinity towards 1,4-dihalobutane and 1,4-bis(imidazol-1-yl)butane. Such an enhanced selectivity is first found in the polypseudorotaxane between pillararene and neutral guests in organic solution and is successfully used for the recognition and adsorption of adiponitrile by the formation of a P1-adiponitrile polypseudorota…
Characterization of semicrystalline random copolymers by small-angle neutron scattering
1979
A new method is introduced to determine the degree of partitioning of noncrystallizable comonomer units (B units) between the two phases of a semicrystalline random copolymer. The method is based on the comparison of the intensities of small-angle neutron and x-ray scattering (SANS and SAXS, respectively). By this technique two quantities can be evaluated: the difference Δρ of the mass densities between the crystalline and the disordered regions, and the concentration fluctuations of the B units in the two phases. It is found that SANS is very sensitive to the presence of small amounts of B units if their scattering length is sufficiently different from that of the A units. This will be the…
Solid polymer electrolytes from a fluorinated copolymer bearing cyclic carbonate pendant groups
2018
International audience; A poly(vinylidene fluoride-co-(2-oxo-1,3-dioxolan-4-yl)methyl 2-(trifluoromethyl)acrylate) random copolymer, poly(VDF-co-MAF-cyCB), with a MAF-cyCB weight fraction of 59% was synthesized via free radical copolymerization of VDF and MAF-cyCB, which is a methacrylate bearing cyclocarbonate side-chain. This copolymer showed nano-structured morphology, where crystalline PVDF-rich domains co-existed with amorphous poly(VDF-co-MAF-cyCB) segments. Solid polymer electrolytes were further obtained by loading the poly(VDF-co-MAF-cyCB) copolymer with various amounts of LiClO4. The added lithium salt was dissolved in the poly(VDF-co-MAF-cyCB) amorphous phase, which allowed the f…
Miscibility of Blends of Biodegradable Polymers and Copolymers with Different Plasticizers
2008
Miscibility between components of different plasticizer(A)/solvent(B)/biodegradable polymer(C) ternary systems with H-bonding has been compared. Systems were formed by two H-donor phenolic plasticizers, 4-nonylphenol (NP) and 4:4'-dihydroxydiphenylmethane (BPF); an H-acceptor solvent, epichlorohydrin (ECH); and H-acceptor poly(3-hydroxybutyrate) (PHB) or poly[(3-hydroxybutyrate)-co-(3-hydroxyvalerate)] (PHBHV) copolymers. Blend miscibility is the result of the balance of three competitive H-bondings: plasticizer self-association (AA), plasticizer-solvent (AB) and plasticizer-polymer (AC) interassociations. The strength and extent of such specific interactions have been experimentally monito…
Crystallinity of block copolymer controlled by cyclodextrin
2018
We report a differential scanning calorimetry study to investigate the effect of cyclodextrins (CD) on the crystallinity of a copolymer. Tetronics was selected as copolymer with star-like shape formed by four polyethylene oxide flanked by four polypropylene oxide blocks linked to ethylenediamine central group. The use of CD with different cavity size was exploited for a block selective inclusion. A model for supramolecular association was considered for a quantitative description of the enthalpy data. The polymer chain incorporation into the CD cavity generates a loss of crystallinity. The stoichiometry of the CD/copolymer aggregates can be tuned by changing the CD cavity size. The investig…
Evolution of the electronic properties of graded poly(thienylene vinylene)-poly(pyrrylene vinylene) mixed copolymers
1993
Abstract We present a valence effective Hamiltonian (VEH) theoretical investigation of the evolution of the electronic properties of poly(thienylene vinylene)-poly(pyrrylene vinylene) mixed copolymers as a function of the unit cell content on the basis of ab initio 3–21G∗ and 3–21G optimized geometries. As a consequence of the strong localization of the LUCO both electron affinity and bandgap deviate from a linear dependence, and only the ionization potential presents the expected values.
Random Copolymers: Their Solution Thermodynamics as Compared with That of the Corresponding Homopolymers
2008
Vapor pressure data (at 50 °C) of solutions of poly(methyl methacrylate) [PMMA], polystyrene [PS], and poly(styrene-ran-methyl methacrylate) [P(S-ran-MMA)], with different weight fractions f of styrene units, in either CHCl3, acetone [AC], methyl acetate [MeAc], or toluene [TL] were evaluated with respect to the dependence of the Flory−Huggins interaction parameter χ on polymer concentration and on f. For all solutions under investigation, χ varies considerably with the composition of the mixture, and only for four of them [CHCl3/PS, AC/PMMA, MeAc/PS, and TL/P(S-ran-MMA) f = 0.5] is this dependence linear; another four systems exhibit a minimum [CHCl3/PMMA, CHCl3/P(S-ran-MMA) f = 0.5, TL/PM…