Removal of Ce(IV) Ions from Aqueous Solutions Using Sawdust Coated by Electroactive Polymers

In this work, adsorption of the Ce(IV) ions onto polypyrrole (PPy) and polyaniline (PAn) conducting electroactive polymers as coated form on sawdust has been investigated. The effect of some important parameters such as initial concentration of the Ce(IV) ion adsorbent dosage, and contact time was studied. The experiments were carried out using both batch and column systems at room temperature. The equilibrium adsorption capacity of sawdust coated by polypyrrole and polyaniline for the removal of Ce(IV) ion was measured and extrapolated using linear Freundlich and Langmuir isotherms. It was found that sawdust modified by PPy and PAn improved the removal efficiency of Ce(IV) ions from aqueous solutions greatly.     

Synthesis of polypyrrole‐modified TiO2 composite adsorbent and its adsorption performance on acid Red G

The adsorption–desorption characteristics of Acid Red G (ARG) on the polypyrrole‐modified TiO₂ (PPy/TiO₂) composite as a novel adsorbent was investigated. PPy/TiO₂ was synthesized via the in‐situ polymerization of pyrrole monomer in the prepared TiO₂ sol solution. Results from X‐ray diffraction and Fourier transform infrared spectra indicated the formation of the PPy/TiO₂ composite. The adsorption experiments showed that the modification of PPy substantially improved the adsorption and regeneration abilities of PPy/TiO₂. The adsorption equilibrium was achieved in a short time of 20 min, and the adsorption kinetics followed the pseudo‐second‐order model. The Langmuir adsorption isotherm was found for PPy/TiO₂, with the maximum adsorption capacity of 179.21 mg/g. The regeneration experiments showed that PPy/TiO₂ could be successfully regenerated by simple alkali‐acid treatment. The adsorption efficiency of the regenerated PPy/TiO₂ adsorbent for ARG was still greater than 90% after regeneration for 10 times. Additionally, the adsorption efficiency of PPy/TiO₂ for the ARG effluent was still higher than 78% after adsorption–desorption for four times. It is expected that the PPy/TiO₂ composite can be considered as a stable adsorbent for the removal of dye. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Composite of cellulosic agricultural waste coated with semiconducting polypyrrole as potential dye remover

A composite was obtained from cellulosic agricultural waste material (Sorghum vulgare) coated with conducting polypyrrole by in situ polymerization using potassium persulfate as chemical oxidant. The composite was characterized by Raman spectroscopy, FTIR spectroscopy, scanning electron microscopy (SEM), and cyclic voltammetry. Aqueous adsorption experiments of methylene blue dye onto the obtained materials at different pH values were conducted. The results showed that this composite is an efficient sorbent for dye removal. The adsorption mechanism was well described by the Langmuir isotherm. The adsorption capacity at neutral pH for uncoated sorghum at an equilibrium concentration (C_e) of methylene blue dye of 10 mg/l was 41.6 mg of dye/g of sorghum and for sorghum/PPy composite was 68.4 mg of dye/gram of composite, which is 1.6 times higher; however, the maxima adsorption capacities were 86.2 and 94.4 mg/g, respectively (only 9.5% more than the uncoated sorghum). It was also observed that at acidic pH for a C_e of 10 mg/l the adsorption capacity of composite was 79.2 mg of dye/gram of composite and the maximum adsorption capacity was 143.5 mg/g (66.4% more than the uncoated sorghum). SEM analysis showed homogeneous coating of cellulosic sorghum material with PPy. Conductivity value of composite was 13.0 × 10⁻³ S/m. Fabrication of this composite should significantly diminish the cost of dye removal from aqueous solutions with respect to some commercial adsorbents. POLYM. COMPOS., 35:186–193, 2014. © 2013 Society of Plastics Engineers     

Adsorption of Th(IV) onto Al-pillared rectorite: Effect of pH, ionic strength, temperature, soil humic acid and fulvic acid

The adsorption of Th(IV) onto Al-pillared rectorite as a function of rectorite concentration, Th concentration, pH, ionic strength, temperature, soil humic acid (HA) and fulvic acid (FA) was studied by using batch technique under ambient condition. The results indicated that the adsorption of Th(IV) onto Al-pillared rectorite strongly depended on pH and ionic strength, and the adsorption of Th(IV) increased with increasing Al-pillared rectorite concentration. The presence of HA/FA enhanced Th(IV) adsorption at low pH and reduced Th(IV) adsorption at high pH. The adsorption of Th(IV) decreased with increasing temperature, indicating that the adsorption process of Th(IV) onto Al-pillared rectorite was exothermic. The experimental data of Th(IV) adsorption were analyzed with the Freundlich and Langmuir models, showing that the Freundlich model fitted the adsorption data better than the Langmuir model. The adsorption of Th(IV) on Al-pillared rectorite may be dominated by surface complexation and cation exchange also contributed partly to Th(IV) adsorption.     

Polypyrrole/NiFe2O4 composites with improved hexavalent chromium removal from aqueous solution

Polypyrrole/NiFe₂O₄ (PPy/NiFe₂O₄) composites were prepared by ultrasonic oxidative polymerization in the presence of NiFe₂O₄ nanoparticles (NPs). The nanostructure of PPy/NiFe₂O₄ was confirmed by the X‐ray diffraction (XRD), scanning electron microscope (SEM), transmission electron microscope (TEM), and vibrating sample magnetometer (VSM) examinations. The adsorption of Cr(VI) onto the PPy/NiFe₂O₄ composite was lowly pH dependent and the adsorption kinetics followed the Pseudo‐second‐order model. The Langmuir isothermal model well described the adsorption isotherm data and the maximum adsorption capacity increased with the increase of temperature. The maximum adsorption capacity of the PPy/NiFe₂O₄ for Cr(VI) ions was up to 50 mg/g at pH 2.0. The excellent adsorption characteristic of PPy/NiFe₂O₄ composite will render it a highly efficient and economically viable adsorbent for Cr(VI) ions removal. POLYM. COMPOS., 38:2779–2787, 2017. © 2015 Society of Plastics Engineers     

A semi-conducting polypyrrole/coffee grounds waste composite for rhodamine B dye adsorption

A composite based on coffee grounds waste (CGW) coated with the semi-conducting polypyrrole (PPy) was prepared by pyrrole polymerization using potassium persulfate as oxidant. The composite was characterized by FTIR spectroscopy, cyclic voltammetry, UV/vis spectroscopy, scanning electron microscopy (SEM) and TGA analysis. SEM analysis showed homogeneous coating of coffee fibers with spherical nanoparticles of PPy with diameters in the range of 200–300 nm. Aqueous adsorption experiments of rhodamine B dye (RhB) onto the as-prepared composite were performed. The effect of pH and initial dye concentration (C₀) on the adsorption behavior was studied. The results showed that this material was an efficient adsorbent of RhB dye at alkaline pH. The adsorption experiments were set at C₀ = 200 mg/L and initial pH values of 2.0, 3.25 and 9.0, the adsorption capacities were 7.22, 13.8, and 19.0 mg of dye/g of the composite, respectively. Nonetheless, when pH was maintained at 9.0 throughout adsorption time, the adsorption capacity increased to 32 mg of dye/g of the composite. When performing adsorption tests using pure CGW, dye adsorption was insignificant at any pH level. Adsorption isotherm for RhB at controlled pH of 9.0 was well described by the Redlich–Peterson model and by the typical Langmuir adsorption model with a theoretical maximum adsorption capacity (q_max) of 50.59 mg of dye/g of composite.     

不同无机酸对聚吡咯/TiO2复合物的吸附性能影响

考察了不同无机酸对PPy/TiO₂复合物吸附性能的影响。首先分别在HNO₃、H₂SO₄和H₃PO₄体系中合成了聚吡咯(PPy)/TiO₂复合物(分别简写为N-PPy/TiO₂、S-PPy/TiO₂和P-PPy/TiO₂)。以红外光谱、热重分析、Zeta电位、比表面积分析和扫描电镜等测试方法对复合物的物理化学性能进行了表征。接着以几种合成的复合对阴离子染料酸性红G和阳离子染料亚甲基蓝进行吸附研究,发现无机酸对合成的复合物的吸附性有较大的影响。几种复合物均可在30min内达到吸附平衡,并且可以重复使用6次以上吸附量没有明显的降低。其中S-PPy/TiO₂的吸附性能最好,其对ARG和MB的最大吸附量分别达到218.34mg/g和314.68mg/g。复合物对染料的吸附过程符合准二级动力学模型和Langmuir吸附等温式。对S-PPy/TiO₂进行吸附热力学研究表明,其对染料的吸附过程为熵增的自发过程。     

Enhanced electrosorption capacity for lead ion removal with polypyrrole and air‐plasma activated carbon nanotube composite electrode

Polypyrrole (PPy) and air‐plasma activated carbon nanotube (CNT) composites (P‐CNT‐PPy) prepared via in situ chemical oxidative polymerization are studied to improve the electrosorption capacity of CNT‐based electrodes for the removal of lead ions. For comparison, the PPy prepared on the CNTs without plasma activation is labeled as CNT/PPy. The morphology of the composite was observed by scanning electron microscopy (SEM), and pore structures were studied by N₂ adsorption‐desorption isotherms. The electrochemical capacitance properties of the composite were measured by cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), and galvanostatic charge‐discharge in lead solutions. With plasma‐activation, the specific surface area of the P‐CNT‐PPy composite is larger than that of CNT/PPy. Additionally, the P‐CNT‐PPy composites exhibit excellent electrochemical performance in lead solution, with a higher specific capacitance and smaller charge transfer resistance than that of CNT/PPy. XPS elemental analysis and electrosorption and regeneration results show that the electrosorption and desorption process is reversible under a voltage of 450 mV. The electrosorption kinetics of P‐CNT‐PPy electrodes abide by pseudo‐second‐order model reaction. The lead ion electrosorption experiments agree with the Langmuir model, and the equilibrium electrosorption capacity of the P‐CNT‐PPy electrodes is 3.6 and 1.3 times higher than that of the CNT and CNT/PPy, respectively. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41793.     

Equilibrium Studies in Adsorption of Hg(II) from Aqueous Solutions using Biocompatible Polymeric Polypyrrole-Chitosan Nanocomposite

This article deals with the adsorption of Hg(II) ions from aqueous solution on biocompatible polymeric polypyrrole-chitosan (PPy/CTN) nanocomposite. The Hg(II) uptake of PPy/CTN was quantitatively evaluated using sorption isotherms. In order to describe the isotherm mathematically, the experimental data of the removal equilibrium were correlated by either the Langmuir, Freundlich and Temkin equations. Results indicated that the Langmuir model gave a better fit to the experimental data than the other two equations. The adsorption capacity (q_max) of PPy/CTN for Hg(II) ions in terms of monolayer adsorption was 40 mg/g.     

聚吡咯/活性炭复合电极对不同离子电吸附性研究

将小阴离子掺杂聚吡咯/活性炭(PPy/AC)复合电极与常规炭电极组装成非对称离子交换膜电容脱盐(MCDI)单元,研究了其对不同荷电量、水合半径离子的吸附性能差异。结果显示:当复合电极分别作为脱盐单元的正极或负极时,其电容吸附过程的离子尺寸依赖效应差异显著,这应该与复合电极氧化还原过程的孔径尺寸变化有关。     

Adsorption of thorium(IV) on MX-80 bentonite: Effect of pH, ionic strength and temperature

The adsorption of Th(IV) on MX-80 bentonite as a function of pH, ionic strength, Th(IV) concentration and temperature was studied by using batch technique. The results indicated that the adsorption of Th(IV) on bentonite depended on pH, ionic strength and temperature. The adsorption of Th(IV) decreased with increasing temperature, indicating that the adsorption process of Th(IV) on bentonite was exothermic. The experimental data of Th(IV) adsorption isotherms were obtained at T = 293, 303, 313, and 323K, and were analyzed with the Langmuir and Freundlich models, showing that the Langmuir model fitted the adsorption data better than the Freundlich model. Thermodynamic parameters, such as ΔH^o, ΔS^o, and ΔG^o, were calculated from the slope and intercept of the linear plot of lnK_d against 1000/T.     

Fabrication of polypyrrole composite on perlite zeolite surface and its application for removal of copper from wood and paper factories wastewater

The large volumes of water used in wood and paper industries produce substantial amounts of wastewater. These industries are among the most polluting ones in the world; there are large quantities of heavy metals (copper, iron, zinc, etc.) and dyes in the wastewater of these industries, and this wastewater has high levels of COD and BOD. We studied copper removal from the effluents of a wood and paper factory by using a polypyrrole composite consisting of natural Zeolite coated on Perlite (PPy/Perlite). The experiments were performed in a batch system in which effects of various parameters including pH, contact time, adsorbent dosage, and temperature on adsorption were studied. Moreover, SEM and FTIR were employed to identify the structure of the synthesized adsorbent. Results indicated that the maximum copper removal (95%) happened at pH=6, contact time of 12 minutes, and adsorbent dose of 0.4 g/100 mL of the wastewater. Furthermore, copper adsorption capacity of the PPy/Perlite adsorbent improved with increases in temperature and reached its peak at 40 °C. Values of the thermodynamic variables (ΔS, ΔH, ΔG) indicated that copper adsorption could occur in the temperature range of 293-323 Kelvin, and was spontaneous and endothermic. Equilibrium information in the studied range of the initial concentrations of copper and in the temperature range suitably matched the Freundlich isotherm. Evaluation of experimental information for studying the kinetics of copper adsorption by PPy/Perlite revealed that copper adsorption followed the pseudo-second-order kinetic model.     

水中Ni~(2+)在粒状沸石/活性炭复合材料上的吸附研究

采用廉价的煤矸石为主要原料,添加一定量的沥青粉制备了沸石NaA/活性炭粒状复合材料,并以此作为吸附剂,研究了水溶液中Ni~(2+)在该复合材料中的吸附行为,考察溶液的初始浓度、吸附时间和pH对吸附的影响.结果表明溶液较高的pH值有利于Ni~(2+)在吸附剂上的吸附;随Ni~(2+)初始浓度的增大复合材料的吸附量增大,而Ni~(2+)的去除率随之减小;Ni~(2+)在复合材料上的吸附接近Langmuir-Freundlich等温吸附模型,反映了吸附表面的多相性及两类吸附中心在复合材料上的共存性;吸附速率遵循准二级吸附动力学模型.     

Synthesis and characterisation of polypyrrole/heparin composites

Polypyrrole heparin composite conducting polymers (PPy/heparin) have been electrochemically synthesised on a quartz crystal electrode. PPy/heparin is electro-active and shows cation exchange properties upon reduction/oxidation. The immobilised heparin can be determined using the toluidine blue assay. Electrochemical quartz crystal microbalance studies show that the heparin in the composite polymer is still active in binding thrombin. In contrast, PPy/heparin has no specific interaction with other test proteins such as BSA or HSA. The morphology of the PPy/heparin composite was investigated using atomic force microscopy.     

Electrodeposited iodide ions imprinted polypyrrole@bismuth oxyiodide film for an electrochemically switched renewable extractor towards iodide ions

Effective extraction and regeneration of radioactive iodide is one of urgent concerns for the safe utilization of nuclear energy. As a novel environmentally benign ion separation technique, electrochemically switched ion extraction(ESIE) process can be applied for effective capture and recovery of iodide ions(I^-). Herein, a novel kelp seaweed-like core/shell I^-imprinted polypyrrole@bismuth oxyiodide(PPy/I^-@BiOI) composite film is successfully prepared for the sel...     

Electrocatalytic reduction of dioxygen at glassy carbon electrodes modified with polypyrrole/anthraquinonedisulphonate composite film in various pH solutions

Functionalized polypyrrole (PPy) film with anthraquinonedisulphonate (AQDS) incorporated as dopant was prepared by anodic polymerization of pyrrole (Py) at a glassy carbon electrode from aqueous solution. The electrochemical behavior of AQDS in PPy matrix and the electrocatalytic reduction of dioxygen on the resulting composite film were investigated in various pH solutions. The formal potential of AQDS and the reduction potential of dioxygen both exhibit pH dependence. In all pH solutions employed, the electrocatalytic reduction of dioxygen at the PPy/AQDS composite film establishes a pathway of irreversible two-electron reduction to form hydrogen peroxide. The pH 6.0 buffer solution is a more suitable medium for the reduction of dioxygen, where the PPy/AQDS composite film showed a more efficient electrocatalytic performance. It was found that AQDS is an effective mediator for the reduction of dioxygen and the reduced AQ is responsible for the enhanced catalytic activity. The catalytic current is under mixed kinetic-diffusion control. The number of electrons transferred and kinetic parameters of dioxygen reduction were determined using cyclic voltammetry, rotating disk voltammetry and Tafel polarization technique.     

EP/氧化石墨烯–硬脂酸丁酯微胶囊复合材料

采用种子微悬浮聚合法制备了聚苯乙烯/氧化石墨烯复合囊壁包覆硬脂酸丁酯微胶囊润滑材料(MGO–Micro LMs),以MGO–Micro LMs为润滑填料,环氧树脂(EP)为基体材料,采用浇注成型工艺制备了EP/MGO–Micro LMs复合材料。采用滑动摩擦磨损试验仪评价了MGO–Micro LMs对EP基体材料摩擦学性能的影响;采用扫描电子显微镜对磨损面的微观形貌进行表征,并探究了其磨损机理。结果表明,MGO–Micro LMs能够显著地降低EP的摩擦系数和磨损量,当MGO–Micro LMs质量分数为20%时,EP/MGO–Micro LMs复合材料的摩擦系数为0.138 44,磨损量减少了约42.3%,磨损机理主要为磨粒磨损。     

A Sponge‐Like 3D‐PPy Monolithic Material for Reversible Adsorption of Radioactive Iodine

3D polypyrrole (3D‐PPy) monolith is prepared by a simple chemical oxidation of pyrrole monomer using FeCl₃ as an oxidant. The as‐prepared PPy monolith exhibits an abundant porosity and with a mesopore size of about 9.1 nm in diameter. Taking advantage of its mesoprous feature as well as the unique chemical composition, the 3D‐PPy is employed as the porous medium for adsorption and removal of radioactive iodine from environment. A high iodine adsorption capacity of 1.6 g g⁻¹ for 3D‐PPy is obtained which is competing with that of those reported porous organic polymers. Besides, the adsorption kinetics and adsorption thermodynamic experiments show that the adsorption is dominated by the pseudosecond‐order kinetics and Langmuir models. Considering its simple and low cost‐effective preparing method, unique monolithic porous as well as π–π conjugated chemical structure, the resulted 3D‐PPy may be found useful applications for removal of radioactive iodine to address environmental issues.     

Ion exchange properties and selectivity of PSS in an electrochemically switchable PPy matrix

A composite of polypyrrole (PPy) and polystyrenesulfonate (PSS) exchanges cations and is a promising material for the technical application of water softening. The ion exchange properties of electrochemically prepared PPy(PSS) are studied by investigating the polymer using a electrochemical quartz crystal microbalance (EQCM) and by analysing the solution surrounding the polymer by atomic adsorption spectroscopy (AAS). The exchange of cations by PPy(PSS) is found to be caused by three driving forces: electrochemical oxidation/reduction of PPy; chemical oxidation of PPy by dissolved oxygen; gradients of cation concentration between polymer and solution. The ion selectivity of PPy(PSS) is investigated and ion exchange isotherms for the binary systems Ca²⁺/Na⁺ and Ca²⁺/Mg²⁺ are determined.     

Polypyrrole/carbon nanotube composites: Molecular modeling and experimental investigation as anti-corrosive coating

In this work we present a computational method based on molecular mechanics (MM) and dynamics (MD), to predict mechanical properties of polypyrrole (PPy)/polyaminobenzene sulfonic acid-functionalized single-walled carbon nanotubes (CNT-PABS) and PPy/carboxylic acid-functionalized single-walled carbon nanotubes (CNT-CA) composites. Furthermore, experiments were carried out to assess the anticorrosive features of the PPy film and CNT-PABS and CNT-CA PPy reinforced composite coatings. Computational bulk models of PPy/CNT-PABS and PPy/CNT-CA were implemented at atomistic scale and composite coatings were grown in situ onto carbon steel (OL 48-50) electrodes. PPy, PPy/CNT-PABS and PPy/CNT-CA computational models and films were investigated concerning mechanical properties by using computational tools. The obtained films were assessed experimentally as anticorrosive materials using potentiodynamic measurements, scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The results clearly confirmed that the CNT-PABS and CNT-CA are properly dispersed in the composite coatings and have beneficial effect on mechanical integrity. Moreover, the anticorrosion protecting ability of the composite coatings is significantly higher than the one characteristic to pure PPy. The Young's moduli generally increased with increasing of CNT content and values ranged from 2.67 GPa in the case of pure PPy to 4.15–4.61 GPa in the case of PPy/CNT-PABS composite system.In agreement with earlier results from the literature for conducting polymer organic coatings, the higher conductivity of material leads to a more efficient anticorrosion protection capability, our results exhibited an enhance of conducting features even for very low mass of CNT-PABS or CNT-CA loaded in composites coatings therefore, an improvement of anticorrosion protecting ability.