The main challenge for the development of a high efficiency supercapacitor is the electrode material. Developing electrode materials with high specific electrical capacitance and low electrical resistance enables an increase in the energy accumulated in the device. In addition, it is expected that the electrode material presents a simple procedure for preparation having low production cost and being environmentally friendly. This work is based on the deposition of silver nanoparticles on activated carbon felt (Ag@ACF) as a supercapacitor electrode. The samples were characterized by field emission gun scanning electron microscopy, X-ray diffraction, X-ray photoelectron spectroscopy and textural analysis. Supercapacitor behavior was evaluated by galvanostatic charge-discharge curves, cyclic voltammetry and electrochemical impedance spectroscopy using a symmetrical two-electrode Swagelok type cell, and three different aqueous solution electrolytes: 2 M H2SO4, 6 M KOH and 1 M Na2SO4. Ag@ACF presented a high specific capacitance in KOH, about 170 F g-1, which makes it an interesting material for supercapacitor electrodes and it showed good specific electrical capacitance, low resistance and high cyclability.

Abstract The aim of this work is to follow the structural variations of polyaniline (PAni) obtained by chemical oxidation on a pre-pilot scale, with different reaction times. Synthesis of PAni is well known, but when it is carried out on a pre-pilot scale, several factors can lead to structural changes and understanding these changes is important to improve controls on the synthesis process. The polymers formed were characterized by spectroscopic techniques (Raman spectroscopy, Fourier Transform Infrared - FTIR and UV-Visible). Degree of oxidation and yield were calculated for each reaction time. The analysis by FTIR, the calculated degree of oxidation and the yield showed significant changes in polymer structure at reaction times of 65 and 80 min. This result was attributed to the excessive oxidation of PAni, with the breaking of its polymer chain. The changes observed in the structure of PAni gave subsidies to the optimization of the process of obtaining polyaniline by chemical synthesis.

ABSTRACT: This paper presents the preparation and characterization of carbon fiber felt and activated carbon fiber felt from textile polyacrylonitrile fiber. Carbon fibers are usually related to aircraft manufacturing or high mechanical purposes. Activated carbon fibers are known as excellent adsorbent materials. Despite all advantages, carbon fiber and activated carbon fiber are expensive materials because of their raw material cost. On the other hand, in this study, carbon fiber felt and activated carbon fiber felt were produced from textile polyacrylonitrile fiber, which is cheaper than their precursor, polyacrylonitrile fiber, and can be converted into carbon fiber felt and activated material with high micropore content and surface area. This research describes the transformation of textile polyacrylonitrile fiber in its oxidized form. After that, the oxidized material was transformed in felt and, in the sequence, converted into carbon fiber felt and activated carbon felt. The carbon fiber felt and activated carbon fiber felt were characterized by X-ray photoelectron spectroscopy, Raman spectroscopy and scanning electron microscope. N2 isotherms were performed to qualify the material obtained for further electrochemical applications. The main result was the conversion dynamics of textile polyacrilonitrile fiber into carbon fiber in felt form and activated carbon fiber in felt with high surface area and high micropores content.

ABSTRACT: Polyanilines have many applications in Aerospace, especially in their doped form. Studies on their synthesis in a pilot scale can contribute to obtain products with desirable characteristics for such applications. The present study reports the chemical oxidative synthesis of polyaniline in pilot scale and different reaction times in order to determine if there are variations in the polyaniline structure, morphology and conductivity due to these synthesis conditions. It is very common to analyze these data for polymers obtained through bench scale. However, several parameters change the properties of final material in major scales, such as thermal, mechanic and diffusive variables. Therefore, the reaction time is the only variable into the 9 syntheses carried out, and polyaniline is obtained in a doped form, being dedoped with ammonium hydroxide and redoped with dodecylbenzenesulphonic acid. The doped and redoped samples were characterized by their molecular structure, thermal behavior, crystallinity and morphology. The electrical conductivity of redoped samples was determined. Some differences in the structure and morphology of doped and dedoped forms, identifying the doping structures, were reported. This paper aims to present the relationship between changes on structure and morphology of doped and undoped polyaniline obtained by the mentioned experiments. Furthermore, some addicts on conductivity are carried out. It was possible to contribute in order to obtain a more conductive polyaniline in pilot scale.

ABSTRACT: The development of polyaniline and graphene oxide composites aims to join the unique properties of each material for aerospace applications. The present paper demonstrates an easy and quick method, compared to the ones found in the literature, to obtain a composite made with polyaniline doped with dodecylbenzenesulfonic acid, a combination commonly called polyaniline, and graphene oxide. Nowadays, the most common studied methods are electrochemistry and in situ chemical polymerization. Differently from these methods, the films were obtained by a physical mixture of equimolar suspension of graphene oxide (4 mg/mL) with 3 concentrations of polyaniline powder: 25; 50 and 75%, being compared to pure graphene oxide and polyaniline. The morphology and structure behavior of all the films were studied, besides the bonding nature between both materials. The films were analyzed by scanning electron microscopy, X-ray diffraction, Fourier transform infrared spectroscopy, and differential scanning calorimetry. The apparent interaction between graphene oxide corrugated sheets and polyaniline grains was verified by scanning electron microscopy images. It can be noticed, as the concentration of polyaniline increases, that more polymer was entrapped. To prove the formation of polyaniline/graphene oxide composite, X-ray diffraction and Fourier transform infrared spectroscopy techniques demonstrated the changes on graphene oxide crystallographic plans and on the chemical bonding between polyaniline and graphene oxide, suggesting an interaction between polyaniline and graphene oxide, especially in the composite with 50% polyaniline/50% graphene oxide. Differential scanning calorimetry was used to highlight this effect through the increase in thermal stability. The method of physical mixture was efficient to obtain the polyaniline/ graphene oxide composites.

The structural and surface properties of reticulated vitreous carbon (RVC) were discussed as a function of its heat treatment temperature (HTT), for samples produced in the range from 700 to 2000 ºC, using the furfuryl precursor resin. The samples were analyzed by x-ray photoelectron spectroscopy, first and second order Raman scattering as well as electrochemical response. Exploring the material turbostraticity concept, the interdependence between the RVC chemical surface variation and its defects were demonstrated. The influence of heteroatom presence was discussed in the material ordering for HTT lower than 1300 ºC while the graphitization process evolution was also pointed out for HTT higher than 1500 ºC.

Electrochemical response of ferri/ferrocyanide redox couple is discussed for a system that uses reticulated vitreous carbon (RVC) three dimensional electrodes prepared at five different Heat Treatment Temperatures (HTT) in the range of 700 °C to 1100 °C. Electrical resistivity, scanning electron microscopy and X ray Diffraction analyses were performed for all prepared samples. It was observed that the HTT increasing promotes an electrical conductivity increasing while the Bragg distance d002 decreases. The correlation between reversibility behavior of ferri/ferrocyanide redox couple and both surface morphology and chemical properties of the RVC electrodes demonstrated a strong dependence on the HTT used to prepare the RVC.