Immobilization of invertase in conducting polymer matrices

Cataloged from PDF version of article.This paper reports a novel approach in the electrode immobilization of an enzyme, invertase, by electrochemical polymerization of pyrrole in the presence of enzyme. The polypyrrolelinvertase and polyamide/polypyrrole/invertase electrodes were constructed by the entrapment of enzyme in conducting matrices during electrochemical polymerization of pyrrole. This study involves the preparation and characterization of polypyrrole/invertase and polyamidelpolypyrrolelinvertase electrodes under conditions compatible with the enzyme. It demonstrates the effects of pH and temperature on the properties of enzyme electrode. Enzyme leakage tests were carried out during reuse number studies. The preparation of enzyme electrodes was done in two different electrolyte/ solvent systems. The enzyme serves as a sucrose electrode and retains its activity for several months. (c) 1997 Elsevier Science Limited. All rights reserve

Polypyrrole grafts with poly[(methyl methacrylate)-CO-(2-(N-pyrrolyl)ethyl methacrylate)]

Cataloged from PDF version of article.Conducting polymer grafts of pyrrole and poly[(methyl methacrylate)-co-(2- (N-pyrrolyl) ethyl methacrylate)] containing 0.7% PEMA units were prepared by potentiostatic anodic polymerization of pyrrole in different electrolytic media. Grafting between copolymer and pyrrole was achieved in media where tetrabutylammonium fluoroborate and sodium perchlorate were used as the supporting electrolytes. Characterizations were made by using IT-IR, DSC, TGA, SEM, CV, and elemental analysis. The conductivities of the resultant polymers seemed to be in the order of pure polypyrrole prepared under the same conditions. Copyright o 1997 Elsevier Scienc

A photoelectron spectroscopic investigation of conducting polypyrolle-polyamide composite film

Cataloged from PDF version of article.X-ray photoelectron spectrum of the electrochemically prepared polypyrrole and polypyrrole-polyamide composite films exhibit an additional strong high binding energy peak at 402.0 eV corresponding to N+ moieties. Intensity of this peak is significantly reduced upon electrochemical reduction. Atomic concentrations derived from the observed N+ and F (stemming from the dopant BF4-) peaks reveal a slightly higher cation/anion ratio for this composite and suggest that the composite has a different chemical composition than the corresponding polymers. © 1995 Elsevier Science B.V.X-ray photoelectron spectrum of the electrochemically prepared polypyrrole and polypyrrole-polyamide composite films exhibit an additional strong high binding energy peak at 402.0 eV corresponding to N+ moieties. Intensity of this peak is significantly reduced upon electrochemical reduction. Atomic concentrations derived from the observed N+ and F (stemming from the dopant BF4-) peaks reveal a slightly higher cation/anion ratio for this composite and suggest that the composite has a different chemical composition than the corresponding polymers

Bioactive surface design based on functional composite electrospun nanofibers for biomolecule immobilization and biosensor applications

Cataloged from PDF version of article.The combination of nanomaterials and conducting polymers attracted remarkable attention for development of new immobilization matrices for enzymes. Hereby, an efficient surface design was investigated by modifying the graphite rod electrode surfaces with one-step electrospun nylon 6,6 nanofibers or 4% (w/w) multiwalled carbon nanotubes (MWCNTs) incorporating nylon 6,6 nanofibers (nylon 6,6/4MWCNT). High-resolution transmission electron microscopy study confirmed the successful incorporation of the MWCNTs into the nanofiber matrix for nylon 6,6/4MWCNT sample. Then, these nanofibrous surfaces were coated with a conducting polymer, (poly-4-(4,7-di(thiophen-2-yl)-1H-benzo[d]imidazol-2-yl) benzaldehyde) (PBIBA) to obtain a high electroactive surface area as new functional immobilization matrices. Due to the free aldehyde groups of the polymeric structures, a model enzyme, glucose oxidase was efficiently immobilized to the modified surfaces via covalent binding. Scanning electron microscope images confirmed that the nanofibrous structures were protected after the electrodeposition step of PBIBA and a high amount of protein attachment was successfully achieved by the help of high surface to volume ratio of electroactive nanofiber matrices. The biosensors were characterized in terms of their operational and storage stabilities and kinetic parameters (K mapp and Imax). The resulting novel glucose biosensors revealed good stability and promising Imax values (10.03 and 16.67 μA for nylon 6,6/PBIBA and nylon 6,6/4MWCNT/PBIBA modified biosensors, respectively) and long shelf life (32 and 44 days for nylon 6,6/PBIBA and nylon 6,6/4MWCNT/PBIBA modified biosensors, respectively). Finally, the biosensor was tested on beverages for glucose detection. © 2014 American Chemical Society

Conducting polymer composites of polypyrrole and polyindene

Polypyrrole-polyindene composites were prepared via electrochemical methods. Two different approaches were utilized. In the first, the electro-initiated polymerization of indene on a platinum electrode was achieved at 2.0 V versus Ag/Ag+ in acetonitrile. Then the polyindene-coated electrode was used for the electrochemical polymerization of pyrrole at 1.0 V versus Ag/Ag+. In the second case, electrochemical coating of platinum electrode with polypyrrole at 1.0 V versus Ag/Ag+ was carried out and indene was polymerized on the conducting polymer at 2.0 V versus Ag/Ag+ in acetonitrile medium. The characterizations of these composites were done by FT-IR, scanning electron microscopy (SEM) and thermal gravimetric analysis (TGA). Electrical conductivities were evaluated by two-probe and four-probe methods

On the possibility of grafting conducting polymers into insulating ones

The possibility of grafting between conducting polymers, like polypyrrole (PPy) and polyaniline (PAn), and insulating polymers, such as polybisphenol A carbonate (PC) and polyamide (PA), is studied via semi-empirical methods using the AM1 parametrization. Several experimental studies on the issue have previously revealed that a chemical interaction exists between the couples (PAn-PC, PPy-PC and PPy-PA) during the electrochemical synthesis of PAn and PPy in the insulating host matrices. Here we present additional theoretical evidence indicating that such grafting is possible, at least for small oligomers

Conducting polymer composites: Polypyrrole and poly (vinyl chloride-vinyl acetate) copolymer

Composites of a polypyrrole (PPy) and poly (vinyl chloride-vinyl acetate) copolymer (PVC-PVA) were prepared both chemically and electrochemically. An insulating polymer was retained in the blend and the thermal stability of the polymer was enhanced by polymerizing pyrrole into the host matrix in both cases. The composites prepared electrochemically gave the best results in terms of conductivity and air stability. © 1997 John Wiley * Sons, Inc

Conducting polymer composites of polypyrrole and a poly(arylene ether ketone)

Electrically conducting composites of polypyrrole and a poly(arylene ether ketone) were synthesized by electroinitiated polymerization of pyrrole on a poly(arylene ether ketone)-coated platinum electrode. The electrolysis medium was water and p-toluene sulfonic acid. The conductivities of the composites were in the range 1-10 S/cm. The composites were characterized by scanning electron microscopy, Fourier transform infrared, and thermal analyses. The composites were found to be composed of bilayers which can be peeled into two free-standing polymer films. The solution side of the polypyrrole layer of the alloy film contains globular structures, whereas the other side is smoother

Conducting polymer composites of polypyrrole and polyimide

Polymeric composites with conductivities ranging from 1 to 10 S/cm were prepared by electrochemically polymerizing pyrrole in a matrix of polyimide. The polyimide/polypyrrole (PI/PPy) composites were characterized by SEM, TGA, FT-IR and electrical conductivity measurements. The cyclic voltammetry technique was used to determine the electroactivity and the electrochemical properties of PPy and PI/PPy. Copyright © 1996 by Marcel Dekker, Inc

Electronic properties of polypyrrole/polyindene composite/metal junctions

Junction properties between conducting polymer composites of polypyrrole/polyindene (PPy/PIn) with different conductivities and metals like Pt, Au, Al and In have been investigated. Rectifying junctions were observed for low work function metals, In and Al; however, high work function metals, Pt and Au, were observed to form ohmic contacts to PPy/PIn composite in the sandwich geometry. The rectifying behavior of the metal/composite/Pt junctions improved when the conductivity of the composite was decreased from 1 to 0.01 S/cm. Using the ideal Schottky theory various junction parameters have been determined. All planar junctions were ohmic regardless of the conductivities of the samples