Synthesis of poly(3,4-propylenedioxythiophene)/MnO2 composites and their applications in the adsorptive removal of methylene blue

AbstractThe poly(3,4-propylenedioxythiophene)/MnO2 composites (PProDOT/MnO2) were prepared successfully by soaking the PProDOT powders into potassium permanganate (KMnO4) solution, with the mass ratio of PProDOT and KMnO4 from 2:1 to 1:2. The structure and morphology of composites were characterized by Fourier transform infrared spectroscopy (FTIR), Raman spectroscopy, ultraviolet–visible absorption spectra (UV), X-ray diffraction (XRD), energy-dispersive X-ray spectroscopy (EDX) and field emission scanning electron microscope (FE-SEM). Furthermore, PProDOT/MnO2 composites were tested as the adsorbents for removal of methylene blue (MB) from aqueous solution. The results revealed that the composites were successfully synthesized, and the thiophene sulfur was oxidized into sulfoxide by KMnO4. The highest percentage removal of MB after 30min was 91% for PProDOT/MnO2 (1:2) composite, and the percentage removal of MB was ~12mgg−1 after 60min at initial concentrations of MB dye of 5.6mgL−1 in the case of PProDOT/MnO2 (1:2) composite. Besides, the adsorption process of PProDOT/MnO2 (1:2) composite was described by pseudo-second-order and Langmuir models

A facile solid-state heating method for preparation of poly(3,4-ethelenedioxythiophene)/ZnO nanocomposite and photocatalytic activity

Poly(3,4-ethylenedioxythiophene)/zinc oxide (PEDOT/ZnO) nanocomposites were prepared by a simple solid-state heating method, in which the content of ZnO was varied from 10 to 20 wt%. The structure and morphology of the composites were characterized by Fourier transform infrared (FTIR) spectroscopy, ultraviolet-visible (UV-vis) absorption spectroscopy, X-ray diffraction (XRD), and transmission electron microscopy (TEM). The photocatalytic activities of the composites were investigated by the degradation of methylene blue (MB) dye in aqueous medium under UV light and natural sunlight irradiation. The FTIR, UV-vis, and XRD results showed that the composites were successfully synthesized, and there was a strong interaction between PEDOT and nano-ZnO. The TEM results suggested that the composites were a mixture of shale-like PEDOT and less aggregated nano-ZnO. The photocatalytic activity results indicated that the incorporation of ZnO nanoparticles in composites can enhance the photocatalytic efficiency of the composites under both UV light and natural sunlight irradiation, and the highest photocatalytic efficiency under UV light (98.7%) and natural sunlight (96.6%) after 5 h occurred in the PEDOT/15wt%ZnO nanocomposite

Solid-State Synthesis and Photocatalytic Activity of Polyterthiophene Derivatives/TiO2 Nanocomposites

Poly(3,4-propylenedioxy-2,2\u27:5\u27,2"-terthiophene)/TiO2 and poly(3,4-(2,2-dimethylenepropylenedioxy)-2,2\u27:5\u27,2"-terthiophene)/TiO2 nanocomposites were synthesized by a simple solid-state method. Additionally, the poly(3,4-propylenedioxy thiophene)/TiO2 and poly(3,4-2,2-dimethylenepropylenedioxythiophene)/TiO2 nanocomposites were synthesized in a similar manner for comparison. The structure and morphology were characterized by Fourier transform infrared (FTIR), ultraviolet-visible (UV-Vis) absorption spectroscopy, X-ray diffraction (XRD) and transmission electron microscopy (TEM). The photocatalytic activities of the nanocomposites were examined through the degradation processes of a methylene blue (MB) solution under UV light and sunlight irradiation. The results of FTIR and UV-Vis spectra showed that the composites were successfully synthesized by solid-state method and the poly(3,4-propylenedioxy-2,2\u27:5\u27,2"-terthiophene)/TiO2 and poly(3,4-(2,2-dimethylenepropylenedioxy)-2,2\u27:5\u27,2"-terthiophene)/TiO2 nanocomposite had a higher oxidation degree and conjugation length than others. The results also indicated that the TiO2 had no effect on the crystallinity of composites, but was well embedded in the polymer matrix. Additionally, the highest degradation efficiency of 90.5% occurred in the case of the poly(3,4-propylenedioxy-2,2\u27:5\u27,2"-terthiophene)/TiO2 nanocomposite

Solid-State Heating Synthesis of Poly (3,4-Ethylenedioxythiophene)/Gold/Graphene Composite and Its Application for Amperometric Determination of Nitrite and Iodate

Abstract A ternary composite of poly (3,4-ethylenedioxythiophene)/gold/graphene (PEDOT/Au/GO) for promising electrochemical sensor was synthesized by solid-state heating method. The interaction between the PEDOT, Au, and GO explored for detection of nitrite and iodate. It was found that the PEDOT/Au/GO composite had shale-like morphology with a uniform distribution of gold nanoparticles. Electrochemical experiments showed that the PEDOT/Au/GO composite modified electrode exhibited good electrocatalytic activity toward determination of iodate. The amperometric experiments at the PEDOT/Au/GO/GCE revealed that a good linear relationship existed between peak current and the concentration in the range of 100–1000 μM with the detection of 0.53 and 0.62 μM (S/N = 3) for nitrite and iodate, respectively. Moreover, the current response of PEDOT/Au/GO/GCE for nitrite and iodate at 10 μM was up to 9.59 and 11.47 μA, respectively. Mechanisms of the direct electron transfer between ion(nitrite or iodate)and the PEDOT/Au/GO composit

Solid-State Synthesis of Polyaniline/Single-Walled Carbon Nanotubes: A Comparative Study with Polyaniline/Multi-Walled Carbon Nanotubes

The polyaniline/single-walled carbon nanotubes (PANI/SWNTs) composites with a content of SWNTs varying from 8 wt% to 32 wt% were synthesized using a solid-state synthesis method. The structure and morphology of the samples were characterized by fourier transform infrared (FTIR) spectra, ultraviolet-visible (UV-vis) absorption spectra, X-ray diffraction (XRD) and transmission electron microscopy (TEM). The electrochemical performances of the composites were investigated by galvanostatic charge–discharge and cycling stability measurements. The structure and properties of PANI/SWNTs were compared with those of PANI/multi-walled carbon nanotubes (PANI/MWNTs) prepared under the same polymerization conditions. The results from FTIR and UV-vis spectra showed that the composites with SWNTs displayed a higher oxidation and doping degree than pure PANI, which is similar to that of PANI/MWNTs. The morphological studies revealed that PANI/SWNTs did not display any rod-like and granular-like features, which appeared in PANI/MWNTs. The galvanostatic charge–discharge measurements indicated that the specific capacitance of PANI/SWNTs is not higher than that of PANI/MWNTs, but the PANI/SWNTs exhibited higher cycling stability and more stable electrochemical behavior in neutral and alkaline electrolytes than PANI/MWNTs

Solid-State Synthesis of Poly(3',4'-dimethoxy-2,2':5',2"- terthiophene): Comparison With Poly(terthiophene) and Poly(3',4'-ethylenedioxy-2,2':5',2"- terthiophene)

A new terthiophene monomer: 3',4'-dimethoxy-2,2':5',2"-terthiophene (TMT) was synthesized and characterized by <sup>1</sup>H-NMR, <sup>13</sup>C-NMR and FTIR. The solid-state oxidative polymerizations of TMT were performed in various ratios of oxidant (FeCl<sub>3</sub>) to monomer (TMT). The resulting polymers were characterized by <sup>1</sup>H-NMR, FTIR, UV-vis-NIR, GPC, X-ray diffraction, CV, as well as TGA and conductivity measurements. The structure and properties of poly (TMT) were compared with those of polyterthiophene [poly(TT)] and poly (3',4'-ethylenedioxy-2,2':5',2"-terthiophene) [poly(TET)] prepared under the same polymerization conditions. After comparative analysis with poly(TT) and poly(TET), the effects of the dimethoxy substituent and FeCl<sub>3</sub> on the structural and physicochemical properties of the poly(TMT)s were discussed in depth. The comparison suggested that the dimethoxy-substituted polymer did not display higher crystallinity, thermal stability, conductivity and electrochemical activity than ethylenedioxy substituted one. The results also showed that the effect of FeCl<sub>3</sub> on poly(TMT) was similar that seen with the poly(TT), in which the oxidation degree, electrochemical activity and conductivity increased steadily with increasing [FeCl<sub>3</sub>]/[TT] ratio. Furthermore, the poly(TMT) and poly(TT) are mostly made up of dimers with a small amount of higher molecular weight components

The Effect of a Small Amount of Water on the Structure and Electrochemical Properties of Solid-State Synthesized Polyaniline

A series of polyaniline (PANI) salts were synthesized with the presence of a small amount of water varying from 0 to 1 mL at the beginning of solid-state polymerization. The structure and morphology of the samples were characterized by fourier transform infrared (FTIR) spectra, ultraviolet-visible (UV-Vis) absorption spectra, X-ray diffraction (XRD) and transmission electron microscopy (TEM). The electrochemical performances of the products were investigated by galvanostatic charge-discharge, cyclic voltammetry, cycling stability and electrochemical impedance spectroscopy (EIS). The results showed that the amounts of water can affect the oxidation degree, conjugate level and crystallinity of PANI salts. All PANI salts showed spherical morphology with the diameter of about 60 nm as shown by TEM. The electrochemical tests showed the highest specific capacitance value 593.3 F.g−1 in 1 M H2SO4 for PANI prepared with the addition of 0.5 mL of water at the beginning of solid-state polymerization