Mária Omastová

Synthesis and structural study of polypyrroles prepared in the presence of surfactants

Abstract Conducting and stable polypyrrole (PPy) was synthesized by chemical oxidative polymerization of pyrrole in aqueous solution containing an oxidant, ferric sulfate, and a surfactant. Anionic surfactants: sodium dodecylbenzenesulfonate, dodecylbenzenesulfonic acid, sodium dodecyl sulfate, poly(ethylene oxide)- n -alkyl-3-sulfopropyl ether potassium salt; cationic surfactant: tetradecyltrimethylammonium bromide; and non-ionic surfactants: poly(ethylene oxide) (10) iso- octylphenyl ether (Triton ® X-100), poly(ethylene oxide) (20) sorbitan monolaurate (Tween ® 20) and poly(ethylene oxide) (20) sorbitan monostearate (Tween ® 60) were used as additives. Results of the elemental analysis and FTIR spectroscopy proved that only the anionic surfactants were incorporated into PPy similarly as the doping anion. This leads to a better stability towards the deprotonation. Also thermal stability, checked by TGA in air, was improved. Scanning electron microscopy studies showed that the presence of the anionic surfactant strongly influenced the morphology of the polymer product.

Electrical properties and stability of polypyrrole containing conducting polymer composites

Abstract Conducting polymer composites of polyethylene and polypyrrole (PE/PPy), polypropylene and polypyrrole (PP/PPy), and poly (methyl methacrylate) and polypyrrole (PMMA/PPy) were prepared by means of a chemical modification method, resulting in a network-like structure of polypyrrole embedded in the insulating polymer matrix. The content of polypyrrole determined by elemental analysis varied from 0.25 to 17 wt.%. Electrical conductivity of compression-moulded samples depends on the concentration of polypyrrole and reached values from 1 × 10 −11 to 1 S/cm. The morphology of the composites was investigated by low-voltage scanning electron microscopy (LVSEM). Potential contrast measurements as a function of the acceleration voltage were used to prove the perfection of the PPy network structure. The electrical transport mechanism in PP/PPy composite was studied. The data of the temperature dependence of conductivity were fitted following the function for a charge-energy-limited tunnelling (CELT) model. There is only a small drop in conductivity caused by annealing of PP/ PPy composites in air at temperatures up to 80 °C. A stabilizing effect of PPy on thermal stability of polypropylene is shown by thermogravimetric analysis. The antistatic properties of PE/PPy and PMMA/PPy composites were demonstrated.

Electrical properties of carbon black-filled polymer composites

This work deals with the dielectric properties of conductive composite materials, which consist of thermoplastic polypropylene (PP) matrix filled with carbon black (CB). The CB concentration was systematically varied in a wide range. Our main interest is focused on the investigation of electrical conductivity mechanism and related percolation phenomena in these materials. To study the electrical and dielectric properties of composites we used broadband ac dielectric relaxation spectroscopy (DRS) techniques in a wide temperature range. By measurements of complex dielectric permittivity, e * , the dependence of ac conductivity, σ ac , and dc conductivity, σ dc , on the frequency, the temperature and the concentration of the conductive filler was investigated. The behavior of this system is described by means of percolation theory. The percolation threshold, Pc, value was calculated to be 6.2 wt. % CB. Both, dielectric constant and dc conductivity follow power-law behavior, yielding values for the critical exponents, which are in good agreement with the theoretical ones. Indications for tunneling effect in the charge carriers transport through the composites are presented. The temperature dependence of dc conductivity gives evidence for the presence of positive temperature coefficient (PTC) effect.

Ultrasensitive Impedimetric Lectin Biosensors with Efficient Antifouling Properties Applied in Glycoprofiling of Human Serum Samples

Ultrasensitive impedimetric lectin biosensors recognizing different glycan entities on serum glycoproteins were constructed. Lectins were immobilized on a novel mixed self-assembled monolayer containing 11-mercaptoundecanoic acid for covalent immobilization of lectins and betaine terminated thiol to resist nonspecific interactions. Construction of biosensors based on Concanavalin A (Con A), Sambucus nigra agglutinin type I (SNA), and Ricinus communis agglutinin (RCA) on polycrystalline gold electrodes was optimized and characterized with a battery of tools including electrochemical impedance spectroscopy, various electrochemical techniques, quartz crystal microbalance (QCM), Fourier transform infrared (FT-IR) spectroscopy, atomic force microscopy (AFM), and X-ray photoelectron spectroscopy (XPS) and compared with a protein/lectin microarray. The lectin biosensors were able to detect glycoproteins from 1 fM (Con A), 10 fM (Ricinus communis agglutinin (RCA), or 100 fM (SNA) with a linear range spanning 6 (SNA), 7 (RCA), or 8 (Con A) orders of magnitude. Furthermore, a detection limit for the Con A biosensor down to 1 aM was achieved in a sandwich configuration. A nonspecific binding of proteins for the Con A biosensor was only 6.1% (probed with an oxidized invertase) of the signal toward its analyte invertase and a negligible nonspecific interaction of the Con A biosensor was observed in diluted human sera (1000×), as well. The performance of the lectin biosensors was finally tested by glycoprofiling of human serum samples from healthy individuals and those having rheumatoid arthritis, which resulted in a distinct glycan pattern between these two groups.

Polypyrrole coating of inorganic and organic materials by chemical oxidative polymerisation

Polypyrrole is one of the most frequently studied conducting polymers, having high electrical conductivity and stability, suitable for multi-functionalised applications. Coatings of chemically synthesised polypyrrole applied onto various organic and inorganic materials, such as polymer particles and films, nanoparticles of metal oxides, clay minerals, and carbon nanotubes are reviewed in this paper. Its primary subject is the formation of new materials and their application in which chemical oxidative polymerisation of pyrrole was used. These combined materials are used in antistatic applications, such as anti-corrosion coating, radiation-shielding, but also as new categories of sensors, batteries, and components for organic electronics are created by coating substrates with conducting polymer layers or imprinting technologies.

Nanocarbon based ionic actuators—a review

Nanocarbons represented especially by carbon nanotubes (CNTs) and graphene have been of great interest during the last two decades, both from a fundamental point of view and for future applications. The most eye-catching features of carbon nanostructures (CNSs) are their electronic, mechanical, optical and chemical characteristics, which open a way for versatile applications. Among those future prospects, actuators are one of the promising technologies. Since 1999 when the first macroscopic actuator containing CNTs was reported, the interest of utilizing these materials as well as other CNSs in active systems has been triggered all over the world. This paper gives a thorough review as well as in-depth descriptions of the many aspects of nanocarbon-based actuators. The review covers aspects of worldwide research and development of nanocarbon ionic actuators up to 2012. Materials which are covered by this review include CNTs and their composites, carbon nanofibres (CNFs), graphene and its derivatives, microporous carbon materials (for example carbide derived carbons (CDCs) and carbon aerogels) as well as the possible combinations of these materials. The considered aspects cover the following fields: synthesis and characterization of the investigated materials, the actuation mechanism as well as modelling and simulation. Applications comprising system integration and device development are also reviewed within this paper. (Some figures may appear in colour only in the online journal)

Polyaniline-coated cellulose fibers decorated with silver nanoparticles

Cellulose fibers of 20 μm in diameter and aspect ratio of 2 or 10 were coated with protonated polyaniline (PANI) during the oxidation of aniline hydrochloride with ammonium peroxydisulfate in an aqueous medium. The presence of PANI has been proved by FTIR spectroscopy. The conductivity increased from 4.0 × 10−14 S cm−1 to 0.41 S cm−1 after coating the fibers with PANI. The percolation threshold in the mixture of original uncoated and PANI-coated fibers was reduced from 10 mass % PANI to 6 mass % PANI, as the aspect ratio changed from 2 to 10. The subsequent reaction with silver nitrate results in the decoration of PANI-coated cellulose fibers with silver nanoparticles of about 50 nm average size. The content of silver of up to 10.6 mass % was determined as a residue in thermogravimetric analysis. FTIR spectra suggest that the protonated emeraldine coating changed to the pernigraniline form during the latter process and, consequently, the conductivity of the composite was reduced to 4.1 × 10−4 S cm−1, despite the presence of silver.

Preparation and characterization of electrically conductive polypropylene/polypyrrole composites

Abstract Polypropylene particles 35 μm in diameter were chemically coated with polypyrrole. The content of polypyrrole varied from 1.1 to 10.4 wt%. Polypropylene/polypyrrole (PP/PPy) composite films about 0.2 mm thick were prepared by compression moulding of modified powders. The electrical conductivity of compression moulded samples depends on the concentration of polypyrrole, and reached values from 4 × 10 −10 to 5 × 10 −3 S cm −1 , which is about seven orders of magnitude higher than the conductivity in the blends prepared by mechanical mixing of PP and PPy in the same PPy concentration range. The PP/PPy composites were characterized by elemental analysis, infrared spectroscopy, light microscopy, scanning electron microscopy (SEM) and thermogravimetric analysis (TGA). SEM pictures showed significant different in coverage of the surface of the PP particles, while the concentration change was within the range from 1.1 wt% to 8.9 wt% PPy.

Electrical and mechanical properties of conducting polymer composites

The method of chemically initiated oxidative modification of polypropylene particles in suspension by pyrrole was used for preparation of conductive polypropylene/polypyrrole composites. Their properties were compared with either polypropylene/polypyrrole composites prepared by melt mixing of virgin polypropylene with chemically synthesized polypyrrole or with polypropylene/carbon black composites prepared also by melt mixing. The composites were characterized by elemental analysis and by mechanical testing. The influence of the processing conditions on the properties of composites is shown. The antistatic properties of prepared composites were demonstrated.

Synthesis, electrical properties and stability of polypyrrole-containing Conducting polymer composites

Conducting polymer composites of polyethylene and polypyrrole (PE/ PPy), polypropylene and polypyrrole (PP/PPy) and poly(methyl methacrylate) and polypyrrole (PPMA/PPy) were prepared by means of a chemical modification method resulting in a network-like structure of polypyrrole embedded in the insulating polymer matrix. The content of polypyrrole determined by elemental analysis varied from 0.25 to 17wt%. Electrical conductivity of compression-moulded samples depended on the concentration of polypyrrole and reached values from 1 x 10 -11 to 1Scm -1 . The morphology of the composites and blends was studied by low-voltage scanning electron microscopy. The stability of PP/PPy composites was investigated by thermogravimetric analysis and by conductivity measurements during heating-cooling cycles. There was only a small drop in conductivity caused by the annealing of PP/PPy composites in air at temperatures up to 80°C. The results of thermogravimetric analysis showed a stabilizing effect of PPy on PMMA/PPy composites against thermal degradation. The antistatic properties of PMMA/PPy composites were demonstrated.