11 research outputs found
Effects of Constant Magnetic Field on Electrodeposition of Co-W-Cu Alloy
The paper presents a study of the effect of constant magnetic field (CMF) on the basic processes of
Co-W-Cu alloys electrodeposition. The alloys electrodeposited in the presence of CMF were more
homogeneous and smooth than those obtained without CMF. The reason for these changes was the fact
that the Lorentz force, generated in CMF, caused the magnetohydrodynamic (MHD) effect. Electrolyte
motion under the influence of CMF caused an increase of cobalt and tungsten content with a
simultaneous decrease of copper content in the alloy. The presence of the magnetic field during plating
leads to significant greater corrosion resistance and smaller roughness
Elektrochemia: wybrane zagadnienia z ćwiczeniami
W ostatnim ćwierćwieczu nastąpił bardzo szybki rozwój elektrochemii. Nowoczesne elektrochemiczne źródła energii, nowe materiały, polimery przewodzące, nanomateriały, sensory i biosensory, rozwój technik pomiarowych, miniaturyzacja sprzętu – to wszystko prowadzi do coraz szerszego zastosowania technologii związanych z elektrochemią we wszelkich dziedzinach życia i nauki. Mamy nadzieję, że książka, którą oddajemy w ręce czytelników, stanie się dla nich przewodnikiem po przedstawionych zagadnieniach współczesnej elektrochemii. Z jednej strony chcemy przybliżyć teoretyczne podstawy wybranych tematów, teorii elektrochemicznych i metod pomiarowych, a z drugiej – pragniemy zaprezentować zbiór instrukcji do ćwiczeń eksperymentalnych wykonywanych w ramach laboratorium z elektrochemii
Effects of serum proteins on corrosion behavior of ISO 5832–9 alloy modified by titania coatings
Stainless steel ISO 5832–9 type is often used to
perform implants which operate in protein-containing physiological
environments. The interaction between proteins and
surface of the implant may affect its corrosive properties. The
aim of this work was to study the effect of selected serum
proteins (albumin and γ-globulins) on the corrosion of ISO
5832–9 alloy (trade name M30NW) which surface was modified
by titania coatings. These coatings were obtained by sol–
gel method and heated at temperatures of 400 and 800 °C. To
evaluate the effect of the proteins, the corrosion tests were
performed with and without the addition of proteins with
concentration of 1 g L−1 to the physiological saline solution
(0.9 % NaCl, pH 7.4) at 37 °C. The tests were carried out
within 7 days. The following electrochemical methods were
used: open circuit potential, linear polarization resistance, and
electrochemical impedance spectroscopy. In addition, surface
analysis by optical microscopy and X-ray photoelectron spectroscopy
(XPS) method was done at the end of weekly corrosion
tests. The results of corrosion tests showed that M30NW
alloy both uncoated and modified with titania coatings exhibits
a very good corrosion resistance during weekly exposition
to corrosion medium. The best corrosion resistance in
0.9 % NaCl solution is shown by alloy samples modified by
titania coating annealed at 400 °C. The serumproteins have no
significant effect onto corrosion of investigated biomedical
steel. The XPS results confirmed the presence of proteins on
the alloy surface after 7 days of immersion in proteincontaining
solutions.The investigations were supported by the National Science Centre project No. N N507 501339. The authors gratefully acknowledge Dr. Janusz
Sobczak and Dr. hab. Wojciech Lisowski from Institute of Physical
Chemistry of PAS for XPS surface analyses
Fabrication and Characterization of an Electrochemical Platform for Formaldehyde Oxidation, Based on Glassy Carbon Modified with Multi-Walled Carbon Nanotubes and Electrochemically Generated Palladium Nanoparticles
This study outlines the fabrication process of an electrochemical platform utilizing glassy carbon electrode (GCE) modified with multi-walled carbon nanotubes (MWCNTs) and palladium nanoparticles (PdNPs). The MWCNTs were applied on the GCE surface using the drop-casting method and PdNPs were produced electrochemically by a potentiostatic method employing various programmed charges from an ammonium tetrachloropalladate(II) solution. The resulting GCEs modified with MWCNTs and PdNPs underwent comprehensive characterization for topographical and morphological attributes, utilizing atomic force microscopy and scanning electron microscopy along with energy-dispersive X-ray spectrometry. Electrochemical assessment of the GCE/MWCNTs/PdNPs involved cyclic voltammetry (CV) and electrochemical impedance spectroscopy conducted in perchloric acid solution. The findings revealed even dispersion of PdNPs, and depending on the electrodeposition parameters, PdNPs were produced within four size ranges, i.e., 10–30 nm, 20–40 nm, 50–60 nm, and 70–90 nm. Additionally, the electrocatalytic activity toward formaldehyde oxidation was assessed through CV. It was observed that an increase in the size of the PdNPs corresponded to enhanced catalytic activity in the formaldehyde oxidation reaction on the GCE/MWCNTs/PdNPs. Furthermore, satisfactory long-term stability over a period of 42 days was noticed for the GCE/MWCNTs/PDNPs(100) material which demonstrated the best electrocatalytic properties in the electrooxidation reaction of formaldehyde
Layer-by-layer (LbL) assembly of polyelectrolytes at the surface of a fiberglass membrane used as a support of the polarized liquid–liquid interface
In this work, the electrified liquid–liquid interface (LLI) was supported with the bare and polyelectrolyte modified fiberglass membranes. The permeability of these supports was then investigated with ion transfer voltammetry (ITV). This work descends from three mutually interconnected experimental tasks. (i) The study of an interfacial behavior of three polyelectrolytes, poly(ethyleneimine) (PEI), polystyrene sulfonate (PSS), and polyhexamethylene guanidine (PHMG) at the polarized LLI. (ii) Electrochemical characterization of the LLI supported by the unmodified fiberglass membrane. (iii) Polyelectrolyte multilayer placement, using layer-by-layer processing, at the surface of the fiberglass membrane and its further utilization as the support for the electrified LLI. Bare and modified membranes were characterized using ITV in the presence of a family of quaternary ammonium cations: tetramethylammonium (TMA+), tetraethylammonium (TEA+), tetrapropylammonium (TPrA+) and tetrabutylammonium (TBA+) initially dissolved in the aqueous phase as the chloride salts. The ionic currents related to their transmembrane transfer were affected already after the first polyelectrolyte layer placement. In addition to electrochemistry, the modification process was followed using several complementary techniques, including optical microscopy (OM), atomic force microscopy (AFM), infra-red (IR) spectroscopy, and scanning electron microscopy (SEM). The proposed methodology offers very simple, fast, and versatile (having in mind the available selection of functional polyelectrolytes) protocol for a membrane preparation having size sieving properties. In turn, the electrochemistry at the LLI can be used as an insightful tool to study the ionic transmembrane currents.</p
Layer-by-layer (LbL) assembly of polyelectrolytes at the surface of a fiberglass membrane used as a support of the polarized liquid–liquid interface
In this work, the electrified liquid–liquid interface (LLI) was supported with the bare and polyelectrolyte modified fiberglass membranes. The permeability of these supports was then investigated with ion transfer voltammetry (ITV). This work descends from three mutually interconnected experimental tasks. (i) The study of an interfacial behavior of three polyelectrolytes, poly(ethyleneimine) (PEI), polystyrene sulfonate (PSS), and polyhexamethylene guanidine (PHMG) at the polarized LLI. (ii) Electrochemical characterization of the LLI supported by the unmodified fiberglass membrane. (iii) Polyelectrolyte multilayer placement, using layer-by-layer processing, at the surface of the fiberglass membrane and its further utilization as the support for the electrified LLI. Bare and modified membranes were characterized using ITV in the presence of a family of quaternary ammonium cations: tetramethylammonium (TMA+), tetraethylammonium (TEA+), tetrapropylammonium (TPrA+) and tetrabutylammonium (TBA+) initially dissolved in the aqueous phase as the chloride salts. The ionic currents related to their transmembrane transfer were affected already after the first polyelectrolyte layer placement. In addition to electrochemistry, the modification process was followed using several complementary techniques, including optical microscopy (OM), atomic force microscopy (AFM), infra-red (IR) spectroscopy, and scanning electron microscopy (SEM). The proposed methodology offers very simple, fast, and versatile (having in mind the available selection of functional polyelectrolytes) protocol for a membrane preparation having size sieving properties. In turn, the electrochemistry at the LLI can be used as an insightful tool to study the ionic transmembrane currents
Layer-by-layer (LbL) assembly of polyelectrolytes at the surface of a fiberglass membrane used as a support of the polarized liquid–liquid interface
In this work, the electrified liquid–liquid interface (LLI) was supported with the bare and polyelectrolyte modified fiberglass membranes. The permeability of these supports was then investigated with ion transfer voltammetry (ITV). This work descends from three mutually interconnected experimental tasks. (i) The study of an interfacial behavior of three polyelectrolytes, poly(ethyleneimine) (PEI), polystyrene sulfonate (PSS), and polyhexamethylene guanidine (PHMG) at the polarized LLI. (ii) Electrochemical characterization of the LLI supported by the unmodified fiberglass membrane. (iii) Polyelectrolyte multilayer placement, using layer-by-layer processing, at the surface of the fiberglass membrane and its further utilization as the support for the electrified LLI. Bare and modified membranes were characterized using ITV in the presence of a family of quaternary ammonium cations: tetramethylammonium (TMA+), tetraethylammonium (TEA+), tetrapropylammonium (TPrA+) and tetrabutylammonium (TBA+) initially dissolved in the aqueous phase as the chloride salts. The ionic currents related to their transmembrane transfer were affected already after the first polyelectrolyte layer placement. In addition to electrochemistry, the modification process was followed using several complementary techniques, including optical microscopy (OM), atomic force microscopy (AFM), infra-red (IR) spectroscopy, and scanning electron microscopy (SEM). The proposed methodology offers very simple, fast, and versatile (having in mind the available selection of functional polyelectrolytes) protocol for a membrane preparation having size sieving properties. In turn, the electrochemistry at the LLI can be used as an insightful tool to study the ionic transmembrane currents.Accepted Author ManuscriptChemE/Advanced Soft MatterOLD ChemE/Organic Materials and Interface