Imidazolium-based ionic liquid type dependence of the bending response of polymer actuators

Actuators based on polymer blends of poly(vinylidene fluoride) (PVDF) with 40 % of different ionic liquids (IL) are prepared by solvent casting. [C2mim][Cl], [C6mim][Cl], [C10mim][Cl], [C2mim][NTf2], [C6mim][NTf2] and [C10mim][NTf2] were selected in order to evaluate the effect of anion and cation sizes in the bending properties. The microstructure, mechanical and electrical properties of the blend depend on the IL type, which in turn leads to a different bending response. In particular, the mechanical properties are independent on the IL type but the AC conductivity of the composites depend more on the anion type than on the size of the alkyl chain connected to the imidazolium based cation. Thus, the bending response of the IL/PVDF composites is correlated with the anion and cation sizes and a maximum bending response of 0.3 % is achieved for a 10 volts square signal in the IL/PVDF composite with 40 wt% content of [C2mim][NTf2].The authors thank FEDER funds through the COMPETE 2020 Programme and National Funds through FCT - Portuguese Foundation for Science and Technology under Strategic Funding UID/FIS/04650/2013, UID/Multi/04551/2013, UID/QUI/50006/2013, project PTDC/EEI-SII/5582/2014, a contract under Investigador FCT 2012 program (J.M.S.S.E.), and grants SFRH/BD/90215/2012 (JCD) and SFRH/BPD/112547/2015 (CMC). Financial support from the Basque Government Industry Department under the ELKARTEK Program is also acknowledged. The authors (R. M. and S. B. H.) would like to thank the Tunisian Ministry of Higher Education and Research for its financial support. The authors thank the support of M. S. Martins (U. Minho) for supporting the electromechanical measurements

The chemical and electrochemical oxidative polymerization of 2-amino-4-tert-butylphenol

[EN] Poly(2-amino-4-tert-butylphenol), poly(2A-4TBP), was synthesized from monomer aqueous solution using either electrochemical or chemical oxidation procedures. Several spectroscopic characterization techniques were employed to gain information on the chemical structure and redox behavior of the obtained materials. It was found that the chemical polymerization product could be described as an oligomer mixture containing up to 16 monomer units. In parallel to other polymers derived from o-aminophenol, phenoxazine rings constitute also the basic structure of poly(2A-4TBP). In addition, the occurrence of N-N couplings, which are favored by the presence of the voluminous tert-butyl substituent, seems also relevant. No significant structural differences were found between the chemically or electrochemically synthesized materials. © 2016 Published by Elsevier Ltd.Financial support from the Spanish Ministerio de Economía y Competitividad and FEDER funds (MAT2013-42007-P) and from the Generalitat Valenciana (PROMETEO2013/038) is gratefully acknowledged. M. Abidi thanks the Ministry of Higher Education and Scientific Research of Tunisia for funding her stay at the University of Alicante.Abidi, M.; López-Bernabeu, S.; Huerta, F.; Montilla-Jiménez, F.; Besbes-Hentati, S.; Morallón, E. (2016). The chemical and electrochemical oxidative polymerization of 2-amino-4-tert-butylphenol. Electrochimica Acta. 212:958-965. https://doi.org/10.1016/j.electacta.2016.07.060S95896521

Effect of anion type in the performance of ionic liquid/poly(vinylidene fluoride) electromechanical actuators

Low voltage actuators based on poly(vinylidene fluoride)(PVDF)with 10, 25 and 40 % 1-hexyl-3-methylimidazolium chloride ([C6mim][Cl])and 1-hexyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide ([C6mim][NTf2]) are prepared by solvent casting in order to evaluate the effect of anion size in the bending properties. Independently of the ionic liquid type and content, its presence leads to the crystallization of PVDF in the -phase. The addition of ionic liquid into the polymer matrix decreases significantly its degree of crystallinity and the elastic modulus. It is also confirmed the good miscibility between PVDF and IL,determinedby the interaction of the CF2groups from the PVDF chains with the imidazolium ring in the ionic liquid (IL). The AC conductivity of the composites depends both on the amount of ionic liquid content and anion size. The bending movement of the IL/PVDF composites is correlated to theirdegree of crystallinity, mechanical properties and ionic conductivity value and the best value of bending response (0.53 %) being found for IL/PVDF composite with40 wt% of [C6mim][Cl] at an applied voltage of 10 volts square signal.The authors thank the FCT-Fundação para a Ciência e Tecnologia-for financial support in the framework of the Strategic Funding UID/FIS/04650/2013, projects PTDC/EEI-SII/5582/2014 and PTDC/CTM-ENE/5387/2014,and grants SFRH/BD/90215/2012 (J.C.D.), SFRH/BPD/112547/2015 (C.M.C.). The authors thank Solvay for kindly supplying the high quality materials. Financial support from the Basque Government Industry Department under the ELKARTEK Program is also acknowledged.The authorsexpress their gratitude to the Ministry of the Higher Education and Scientific Research of Tunisiafor a research fellowship

Voies de valorisation des pulpes de dattes.

peer reviewe

A self-doped polyaniline derivative obtained by electrochemical copolymerization of aminoterephthalic acid and aniline

[EN] The electrochemical copolymerization of aminoterephthalic acid and aniline can be achieved to yield a self-doped material showing electroactivity at physiological pH. The present study focusses on the management of the synthesis conditions to obtain a true copolymerization product and to control the relative amount of both comonomers eventually incorporated to the copolymer chain. Both, in situ FTIR spectroscopy and ex situ XPS techniques proved the successful incorporation of aminoterephthalic acid and, in parallel to other polyaniline parent derivatives, revealed the existence of redox transformations involving leucoemeraldine-emeraldine-pernigraniline transitions. The use of a high inversion potential (1.4¿V/RHE) during electro-copolymerization resulted in a material enriched in aminoterephthalic acid fraction with respect to aniline, while this last component is favored at lower potentials. The pH behavior of copolymers in combination with in situ FTIR results strongly suggested that a larger content of aminoterephthalic acid (such as that obtained after deposition at 1.4¿V) do not ensure an extensive self-doping process because a significant fraction of those carboxylic moieties remain inactive during the redox transformation. Instead, low inversion potentials are preferred to obtain a material with less defects and thoroughly electroactive at physiological pH.Financial support from the Spanish Ministerio de Economia y Competitividad and FEDER funds (MAT2016-76595-R) is gratefully acknowledged. S. Dhkili thanks the Ministry of Higher Education and Scientific Research of Tunisia for funding her stay at the University of Alicante.Dkhili, S.; López-Bernabeu, S.; Huerta, F.; Montilla-Jiménez, F.; Besbes-Hentati, S.; Morallón, E. (2018). A self-doped polyaniline derivative obtained by electrochemical copolymerization of aminoterephthalic acid and aniline. Synthetic Metals. 245:61-66. https://doi.org/10.1016/j.synthmet.2018.08.005S616624

Elaboration of an Imprinted Polymer Film Based on Chitosan Electrodeposition for the Voltammetric Detection of BPA

International audienc

The Influence of the Chemical Structures of Chitosan and Acid Dye on the Adsorption Process

The objective of this paper is the study of the influence of the chemical structures of adsorbent and adsorbate on the adsorption process. By using of crab shell chitosan (CC) and deep-pink shrimp chitosan (CP) for removal of acid 183 and AR114 from aqueous solutions, it is shown that CP, which corresponds to the highest molecular weight, is the most efficient adsorbent material. In addition, the best extent of decolorization is obtained for AR 183 that is the smallest molecule. Langmuir model represents the best fit of the experimental data, indicating monolayer coverage of chitosan outer surface. Pseudo-second order kinetic model describes accurately the adsorption processes, suggesting chemical rate limiting steps. The positive values of the enthalpy changes indicated endothermic attachment of dyes to the biomaterials. CP/AR183 system corresponds to the most energetically favorable phenomenon. Besides, desorption of AR from chitosan was found to be very low in acidic aqueous medium for all couples