Search results for "Electrolyte"
showing 10 items of 746 documents
Ionic partition diagram of tetraphenylporphyrin at the water|1,2-dichloroethane interface
2011
diagram of 5,10,15,20-tetraphenyl-21H,23H-porphine (H2TPP) at the water|1,2-dichloroethane interface using a simple Born solvation model. This zone diagram shows under which form this porphyrin is present, i.e. neutral, monoprotonated or diprotonated, and in which phase i.e. either in the aqueous or the organic phase as a function of the aqueous pH and the interface polarisation that can be controlled externally or by the distribution of supporting electrolytes. This diagram explains why the monoprotonated form has been difficult to observe when doing biphasic pH titrations
GROWTH AND PHOTOELECTROCHEMICAL BEHAVIOUR OF ELECTRODEPOSITED ZnO THIN FILMS FOR SOLAR CELLS
2012
Thin zinc oxide films were deposited potentiostatically from zinc nitrate aqueous solutions on ITO substrates. The influence of experimental parameters (temperature, electrolyte concentration, deposition potential) on structure and morphology of films was investigated. Deposited films were generally polycrystalline in structure, even if growth according to preferential planes occurs in certain conditions. The effect of thermal treatments in air at 150 and 350 °C was also studied. In some cases, Cl species were incorporated into deposit by adding zinc chloride to the electrolyte. A photoelectrochemical investigation, performed in neutral solution before and after thermal treatment, gives mor…
Electrochemical reduction of graphene oxide films in aqueous and organic solutions
2013
Abstract Electrochemical reduction of graphene oxide (GO) films cast on tin oxide glass substrates were carried out in aqueous solutions and in propylene carbonate and acetonitrile. Cyclic voltammetric measurements indicate successful reduction of GO films. The reduction process begins in aqueous solutions at less negative potentials than in organic solutions. Additionally the pH value of the aqueous solutions influences the reduction potential. According to spectroscopic analysis the reduction process of the GO film can be controlled by the choice of reduction potential and electrolyte medium. The potential window in this work was made broader by increasing pH or by using organic electroly…
Cation and anion electrochemically assisted solid-state transformations of malachite green
2020
[EN] The possibility of the electrochemical promotion of different solid-to-solid transformations including the performance of successive cation and anion insertion processes has been tested using malachite green, a triphenylmethane dye, in contact with aqueous NaCl electrolyte. Electrochemical data using the voltammetry of microparticles methodology reveal significant differences with the solution phase electrochemistry of the dye. Voltammetric data, combined with atomic force microscopy, focusing ion beam-field emission scanning electron microscopy, and high-resolution field emission scanning electron microscopy permit characterization of the oxidative dissolution, oxidation with anion in…
Electrochemical conversion of pressurized CO2 at simple silver-based cathodes in undivided cells: study of the effect of pressure and other operative…
2020
Abstract Electrochemical reduction of pressurized CO2 is proposed as an interesting approach to overcome the main hurdle of the CO2 electrochemical conversion in aqueous solution, its low solubility (ca. 0.033 M), and to achieve good faradaic efficiency in CO using simple sheet silver cathodes and undivided cells, thus lowering the overall costs of the process. The effect on the process of CO2 pressure (1–30 bar), current density, nature of the supporting electrolyte and other operative conditions, such as the surface of the cathode or the mixing rate, was studied to enhance the production of CO. It was shown that pressurized conditions allow to improve drastically the current efficiency o…
Degradation of passive layers of iron studied by conversion electron Mössbauer spectroscopy
1995
Integral electron Mossbauer spectroscopy (ICEMS) and additionally some electrochemical methods were used to characterize the passivation process of iron (low carbon steel) in sulfate, sulfate+sulfite (a possible model solution of acid rain) solutions and in phosphate buffer. The phase compositions and thicknesses of the passive layers formed due to the electrochemical polarizations were analyzed in dependence on the duration of the anodic passivations and on the pH of the used electrolytes. The passive layer, as determined from the Mossbauer spectra, consists mainly of γ-FeOOH, however in sulfite confining sulfate aqueous solution at pH 3.5 Fe 3 C and despite ex-situ circumstances FeSO 4 .H…
New Self-Assembling Polyaspartamide-Based Brush Copolymers Obtained by Atom Transfer Radical Polymerization
2009
A simple and efficient method for the synthesis of polyaspartamide-based brush copolymers using Atom Transfer Radical Polymerization (ATRP) is here presented. The syntheses were performed by using two subsequent steps. In the first step the macroinitiator was obtained by the conjugation of a proper number of 2-bromoisobutyryl bromide (BIB) residues to the R, -poly(N-2-hydroxyethyl)-D,L-aspartamide (PHEA) side chains, obtaining the PHEA-BIB copolymer. PHEA-BIB copolymer was used as “multi-functional macroinitiator” for the polymerization via ATRP of hydrophilic methacrylic monomers, such as methacrylic acid (MA), obtaining PHEA-IB-poly(MA) copolymer, sodium methacrylate (MANa+), obtaining PH…
Polyacrylates in aqueous solution. The dependence of protonation on molecular weight, ionic medium and ionic strength
2003
Abstract The protonation constants of polyacrylates with different molecular weights ( W =2000–750 000 Da) were determined in different ionic media (alkali metal chlorides and nitrates, tetraalkylammonium chlorides), at 25 °C, by potentiometric measurements (H + –glass electrode). Literature data were also considered. Different models used to analyse protonation data were compared: the first was the modified Henderson–Hasselbalch two-parameter equation, and the second was the three-parameter equation proposed by Hogfeldt. The dependence on the ionic strength of the different supporting electrolytes and all the protonation parameters involved in the two models showed the trend Et 4 N + ≫Li +…
Static and dynamic light scattering by aqueous polyelectrolyte solutions: effect of molecular weight, charge density and added salt
1990
Abstract Aqueous solutions of quaternized poly(2-vinylpyridine) were investigated by static (SLS) and dynamic (DLS) light scattering over a wide range of polyelectrolyte, c pe , and salt concentrations, c s (10 −3 ≤ c pe ≤ 10 2 gl −1 , 10 −5.5 ≤ c s ≤ 10 −1 moll −1 ). Using DLS the cooperative diffusion coefficient D was measured as a function of c pe and c s . D exhibits a characteristic behaviour in each of three different concentration regimes. In the ‘dilute lattice’ regime, where λ = c pe c s ⪡ 1 , one diffusion coefficient is observed. In the transition regime, where λ ≈ 1, D increases with increasing polyelectrolyte concentration and a slow diffusive mode gradually appears. For λ ⪢ 1…
Investigation of the Interpolymer Complex between Hydroxypropyl Cellulose and Maleic Acid-Styrene Copolymer, 1
2004
The hydrogen bonding-interpolymer association of hydroxypropyl cellulose (HPC) with maleic acid-styrene (MAc-S) copolymer has been investigated in dilute aqueous solution by viscometry, turbidimetry and potentiometry. At a mixing ration between MAc-S and HPC of 10:90, the solution exhibits a phase separation upon heating, while for other mixing ration no phase separation could be detected. The stability of the interpolymer complex (IPC) increases as the temperatures rises. The stoichiometry of the IPC, in mole units, was estimated as being MAc-S:HPC=5:2. The thermodynamic functions (enthalpy and entropy) of the complexation process have been determined.