Electromagnetic interference shielding characteristics of fabric complexes coated with conductive polypyrrole and thermally evaporated Ag

Through the chemical coating of polypyrrole (PPy) doped with naphthalene sulfonic acid (NSA) on electrically insulating poly (ethylene terephthalate) (PET) woven fabric, PPy–NSA/PET complexes were synthesized. By using the electrochemical coating of PPy doped anthraquinone-2-sulfonic acid (AQSA) on PPy–NSA/PET complexes, PPy–AQSA/PPy–NSA/PET complexes were synthesized. The silver (Ag) was thermally vacuum evaporated on the surface of PPy–AQSA/PPy–NSA/PET complexes (Ag|PPy–AQSA/PPy–NSA/PET). Electromagnetic interference (EMI) shielding efficiency (SE) and dc conductivity (σ_dc) of fabric complexes were measured for EMI shielding characteristics and theoretical simulation. The measurement of EMI SE in the frequency range from 50 MHz to 1.5 GHz was performed by using ASTM D4935-99 method. The EMI shielding characteristics such as transmittance, reflectance and absorbance were obtained from the S (scattering)-parameter analysis. We control the contribution of the absorbance or the reflectance to total EMI SE through the coating of conductive PPy and the evaporation Ag.     

Electrochemistry of platinum nanoparticles supported in polypyrrole (PPy)/C composite materials

Conducting polypyrrole (PPy)/C (Vulcan XC-72) composite materials were synthesized by chemical polymerization method. These materials were used as matrix to support platinum nanoparticles, which were produced by the carbonyl chemical route. For the same catalyst loading (50 μg cm⁻²), it was observed that the nature of the composite strongly influences the electrochemical activity of nanoparticulated platinum toward the oxygen reduction reaction in acid medium. The variation of the PPy/C ratio determines the so-called substrate effect for electrocatalysis. Dedicated to Prof. Dr. Teresa Iwasita on the occasion of her 65th birthday in recognition of her numerous contributions to interfacial electrochemistry.     

Regenerable Leptin Immunosensor Based on Protein G Immobilized Au‐Pyrrole Propylic Acid‐Polypyrrole Nanocomposite

A regenerable, labelless electrochemical immunosensor is investigated. In this work, pyrrole (Py) and pyrrole propylic acid (Pa) were co‐electropolymerized in the presence of gold nanoparticles to form a porous, conductive, stable and hydrophilic nanocomposite, followed by the covalent attachment of protein G to capture an antibody as the probe for the immunoassay. The regeneration of the sensor was achieved by rinsing the electrodes with 0.1 M glycine buffer (pH 2.7). The binding and dissociation of the antibody with protein G and optimization of the efficient immobilization were studied by impedance and optical measurements, respectively. The charge transfer resistance obtained from the impedance measurements is used to study the interaction between antibody‐protein G and antibody‐antigen. The immunosensor performance and its regenerability were evaluated by using anti‐leptin IgG as the probe protein to detect leptin in 0.01 M PBS, and its specificity was tested in 1% human serum. The leptin impedimetric immunosensor exhibits a detection dynamic range of 10–100 000 ng/mL with 10 ng/mL detection limit in 0.01 M PBS+1% serum solutions. This work proves the feasibility to make a sensitive, regenerative electrochemical immunosensor, which could be very useful for environmental control and food analysis.     

本征导电聚合物涂层及界面

本文结合我们实验研究结果及国外最近的研究进展，对在绝缘基质的表面本征导电聚合物涂层的形成、结构和性能作了扼要的分析，指出了化学反应法中通过单体向整体聚合物表层扩散聚合形成的导电膜、界面的偶联作用和电荷转移作用等几种新近证实的原理，在加速导电聚合物涂层的应用中，具有重要意义。     

Synthesis of a graphene‐based nanocomposite for the dispersive solid‐phase extraction of vancomycin from biological samples

The approach of this work was to study the capability of graphene‐based materials in the field of biological sample preparation. A polypyrrole/graphene composite was synthesized and characterized. The potential of the nanocomposite was investigated as a sorbent in dispersive solid‐phase extraction followed by high‐performance liquid chromatography with UV detection for vancomycin as a model drug. The effect of different parameters influencing extraction efficiency such as sample pH and sample volume, ionic strength, extraction time, type, and volume of desorption solvent and desorption time were investigated. A comparison study was also conducted between polypyrrole/graphene and some different novel and classic sorbents. Under optimized conditions, the calibration curve for vancomycin showed linearity in the range of 0.05–10 μg/mL. In addition, limits of detection, and quantification were 0.003 and 0.01 μg/mL, respectively. The intraday and interday relative standard deviations at a concentration of 0.05 μg/mL (n = 3) were 1.6 and 2.1%, respectively. Furthermore, the proposed method was successfully applied for the determination of vancomycin in plasma and urine samples. The relative recoveries indicated the feasibility of graphene‐based sorbents in biological sample analysis.     

Polypyrrole/silica/magnetite nanoparticles as a sorbent for the extraction of sulfonamides from water samples

A magnetic solid‐phase extraction sorbent of polypyrrole/silica/magnetite nanoparticles was successfully synthesized and applied for the extraction and preconcentration of sulfonamides in water samples. The magnetite nanoparticles provided a simple and fast separation method for the analytes in water samples. The silica coating increased the surface area that helped to increase the polypyrrole layer. The polypyrrole‐coated silica provided a high extraction efficiency due to the π–π and hydrophobic interactions between the polypyrrole and sulfonamides. Several parameters that affected the extraction efficiencies, i.e. the amount of sorbent, pH of the sample, extraction time, extraction temperature, ionic strength, and desorption conditions were investigated. Under the optimal conditions, the method was linear over the range of 0.30–200 μg/L for sulfadiazine and sulfamerazine, and 1.0–200 μg/L for sulfamethazine and sulfamonomethoxine. The limit of detection was 0.30 μg/L for sulfadiazine and sulfamerazine and 1.0 μg/L for sulfamethazine and sulfamonomethoxine. This simple and rapid method was successfully applied to efficiently extract sulfonamides from water samples. It showed a high extraction efficiency for all tested sulfonamides, and the recoveries were in the range of 86.7–99.7% with relative standard deviations of < 6%.     

Electrochemically controlled in-tube solid phase microextraction

We report a new in-tube solid phase microextraction approach named electrochemically controlled in-tube solid phase microextraction (EC in-tube SPME). This approach, which combined electrochemistry and in-tube SPME, led to decrease in total analysis time and increase in sensitivity. At first, pyrrole was elctropolymerized on the inner surface of a stainless steel tube. Then, the polypyrrole (PPy)-coated in-tube SPME was coupled on-line to liquid chromatography (HPLC) to achieve automated in-tube SPME–HPLC analysis. After the completion of EC-in-tube SPME–HPLC setup, the PPy-coated tube was used as working electrode for uptake of diclofenac as target analyte. Extraction ability of the tube in presence and in absence of applied electrical field was investigated. It was found that, under the same extraction conditions, the extraction efficiency could be greatly enhanced by using the constant potential. Important factors are also optimized. The detection limit (S/N = 3) and precision were 0.1 μg L⁻¹ and 4.4%, respectively.     

聚吡咯/纳米SiO_2复合材料的制备及氧化性能

采用化学氧化法制备聚吡咯/纳米Si O2(PPy/n Si O2)复合材料,通过扫描电子显微镜和红外光谱对其进行表征,并将其应用到对苯二酚的氧化反应中.结果表明,PPy/n Si O2复合材料中,PPy较均匀地负载在纳米Si O2表面.在弱酸性介质中,PPy/n Si O2对对苯二酚具有很好的氧化性能.反应2 h内,对苯二酚的氧化过程符合表观一级反应动力学.结合紫外-可见光谱法分析表明,聚吡咯通过与对苯二酚之间的氢键相互作用形成聚吡咯活性中间体,将对苯二酚氧化为对苯醌,聚吡咯具有氧化剂和催化剂的双重功能.     

聚吡咯/多壁碳纳米管及其聚氨酯导电复合材料的制备和性能

以羧基化多壁碳纳米管(MWCNTs)做模版剂,采用化学氧化法将吡咯(Py)在羧基化MWCNTs表面聚合制备PPy/MWCNTs导电材料,将其添加到溶剂型聚氨酯(PU)溶液中制备了PPy/MWCNTs/PU导电复合材料,研究了Py用量对PPy/MWCNTs及其PU复合材料性能的影响.研究表明,随Py用量的增加,PPy/MWCNTs的长度不变,管径增大,sp~2和sp~3杂化C含量先提高后减少,N的掺杂梯度降低,PPy/MWCNTs的导电率高于羧基化MWCNTs和PPy.当Py用量为羧基化MWCNTs的20%时,其导电率最大.PPy/MWCNTs中N元素的掺杂程度及其管径变化是引起PPy/MWCNTs/PU复合材料的性能不同的主要原因.增加Py用量,MWCNTs中亲水的羧基因对PPy掺杂而消耗,相同导电材料用量时纳米导电粒子数目相对减少,PPy/MWCNTs/PU复合材料的耐水性能提高,定向应力、储能模量和玻璃化温度降低,导电率先增加后减小.当Py用量为羧基化MWCNTs的15%时,导电率最大.