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1.
Ultrasonic irradiation is employed to assist the chemical oxidative polymerization of aniline in the presence of Fe3O4 nanoparticles in order to prepare a polyaniline (PANI)/Fe3O4 magnetic nanocomposite. In the chemical oxidative polymerization of aniline in the initially neutral medium, the optimum molar ratio of the oxidant ammonium persulfate to the monomer aniline is 2 : 1. The prepared PANI is in the emeraldine form and is doped by sulfate anions. Fe3O4 particles are encapsulated by PANI and dispersed well in PANI. Fe3O4 increases the doping level and decreases the crystallinity of PANI. The PANI/Fe3O4 nanocomposite possesses conductivity and magnetic properties. Increasing the Fe3O4 content increases the magnetization of the PANI/Fe3O4 composite but decreases its conductivity. © 2006 Wiley Periodicals Inc. J Appl Polym Sci 102: 2107–2111, 2006  相似文献   

2.
Different nanostructured polyaniline (PAni) has been synthesized via facile template‐free electrochemical synthesis approach in aqueous medium. Instead of conventionally used aniline, aniline sulphate was used in electrochemical polymerization. The synthesis process involves simultaneous doping with combination of inorganic and organic acid, i.e., sulfuric acid (H2SO4) and p‐toluenesulfonic acid (PTSA) at different ratios keeping total dopant concentration constant. Synergistic increase in conductivity is observed and the best conductivity is achieved at 3:1 ratio of [H2SO4]:[PTSA]. Different nanostructures of PAni are revealed through morphological analysis consisting of nanosphere, nanorod, and clustered particles among which finer nanorods show the best electrical conductivity. Upon controlled heat treatment followed by further cooling, resistivity increases, but after one day it decreases again and in the optimized dual doped PAni, it approaches approximately the same value of initial resistance. Lattice strain and benzenoid to quinonoid ratio increases with heat treatment. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013  相似文献   

3.
Polyaniline/Ag nanocomposites have been synthesized via in situ chemical oxidation polymerization of aniline in silver salt by sonochemical method using H2O2 as an external medium. H2O2 was used to reduce AgNO3 to Ag nanoparticles as well as to polymerize aniline to polyaniline in the same pot. The ultrasound radiation as an energy source was applied to facilitate the reaction by reducing the reaction time. Reduction of the silver salt in aqueous aniline leads to the formation of silver nanoparticles which in turn catalyze oxidation of aniline to polyaniline. The research on the structures and properties of the composites showed the individual or aggregated silver nanoparticles are dispersed in the matrix of polyaniline. The composites possess a higher degradation temperature than polyaniline alone, and their electrical conductivity are raised morethan 200 times. The cyclic voltammetry and impedance spectroscopy results showed that the polyaniline/Ag film exhibits considerably higher electroactivity compared with polyaniline film without Ag particles. POLYM. COMPOS., 31:1662–1668, 2010. © 2009 Society of Plastics Engineers  相似文献   

4.
A series of conductive nanocomposites cellulose/reduced graphene oxide/polyaniline (cellulose/RGO/PANi) were synthesized via in situ oxidative polymerization of aniline on cellulose/RGO with different RGO loading to study the effect of RGO on the properties of nanocomposites. The results showed that when RGO is inserted into cellulose/PANi structure, its thermal stability and conductivity are increased. So that adding of only 0.3 wt% RGO into the cellulose/PANi structure, its conductivity is increased from 1.1 × 1 10?1 to 5.2 × 110?1 S/cm. Scanning electron microscopy results showed that the PANi nanoparticles are formed a continuous spherical shape over the cellulose/RGO template; this increases the thermal stability of nanocomposite.  相似文献   

5.
Conductive polyaniline was synthesized in aqueous 1.0M oxalic acid containing 0.1 M aniline by electrochemical and chemical oxidation and characterized by conductivity, solubility, ultraviolet and infrared spectroscopy, and cyclic voltammetry. The solubility experiments showed that the solubility of oxalic acid-doped polyaniline in dimethylsulfoxide and dimethylformaide increased to a certain extent. The soluble part of the polyaniline was free from impurities such as quinones. Cyclic voltammetric studies in oxalic acid medium revealed that aniline exhibited a similar behaviour to that in H2SO4 and the polymerization rate was much slower than that in H2SO4.  相似文献   

6.
Polyaniline (PANI) has been blended with cellulose triacetate (CTA) to obtain both good mechanical properties and good electrical properties. The effects of PANI weight percentage on the optical, structural, morphological and electrical properties in the blend films of polyaniline and cellulose triacetate (PANI/CTA) have been investigated. The phenomenon of percolation was observed in these blend films. It is found that the electrical conductivity of the blend films increases with the increase of polyaniline content up to a value of 10−4 S cm−1 at 84 weight percentage of PANI. The experimental percolation threshold of the dried blend films is obtained at 9.5 wt% of polyaniline. The values of Mott’s temperature, density of states at the Fermi level [N (E f)], hopping distance (R hop), and barrier height (W hop) for PANI/CTA blend films are calculated. By applying Mott’s theory, it is found that the PANI/CTA blend films obey the three dimensional variable range hopping mechanism.  相似文献   

7.
Polyaniline is prepared by chemical polymerization of aniline in an acidic solution using H2O2 as an oxidant and ferrous chloride as a catalyst. A wide variety of synthesis parameters are studied, such as the amount of the catalyst, reaction temperature, reaction time, initial molar ratio of oxidant, monomer and catalyst, and aniline and HCl concentrations. The polymerization of aniline can be initiated by a very small amount of catalyst. The yield and the conductivity of product depend on the initial molar ratio of the oxidant and monomer. The polyaniline with a conductivity of about 10° S/cm and a yield of 60% is prepared under optimum conditions. The process of polymerization was studied by in situ ultraviolet–visible spectroscopy and open‐circuit potential technology. Compared to the polymerization process in a (NH4)2S2O8 system, the features of the H2O2 Fe2+ system are pointed out, and the chain growth mechanism is proposed. © 1999 John Wiley & Sons, Inc. J Appl Polym Sci 72: 1077–1084, 1999  相似文献   

8.
In this report, a novel chemical synthesis of polyaniline/gold nanocomposite is explored using ionic liquid (IL) 1-Butyl-3-methylimidazolium hexafluorophosphate. The direct chemical synthesis of polyaniline/gold nanocomposite was initiated via the spontaneous oxidation of aniline by AuCl4 in IL. A nearly uniform dispersion of polyaniline/Au particles with a diameter of 450 ± 80 nm was produced by this method, which indicates that this method is more suitable for controlling particle dimensions. It was also found that the electrical conductivity of the polyaniline/gold nanocomposite was more than 100 times higher than that of the pure polyaniline nanoparticles. The polyaniline/gold nanocomposite displays superior function in the biocatalytic activation of microperoxidase-11 because of the high surface area of the assembly and the enhanced charge transport properties of the composite material. We also report the possible application of polyaniline/gold nanocomposite as a H2O2 biosensor.  相似文献   

9.
Highly conducting nylon-6 composites are synthesized by exposing nylon-6 films or fabrics impregnated with an oxidizing agent, cupric chloride, simultaneously to aniline and hydrochloric acid vapors. The conductivity of composite films reaches up to 10?2 S/cm and can be controlled by varying the experimental conditions for the composite synthesis. The effects of the concentration of cupric chloride, exposure time to aniline and hydrochloric acid vapors, and concentration of hydrochloric acid to the polyaniline content and the conductivity of nylon-6/polyaniline composites are analyzed by means of statistical F test. The morphology change of composite films resulting from the synthesis conditions, conductivity in relation to the morphology, and stability of conductivity to ambient air exposure have been investigated.  相似文献   

10.
A water‐dispersible conducting polyaniline/ nano‐SiO2 composite, with a conductivity of 0.071 S cm?1 at 25°C, was prepared by the oxidative polymerization of aniline in the presence of amorphous nano‐SiO2 particles. And the structure, morphology, thermal stability, conductivity, and electroactivity of this composite were also investigated. This composite has been steadily dispersed in the aqueous solution for about 10–36 h without the need for any stabilizer. It would significantly impulse the commercial applications of conducting polyaniline/nano‐SiO2 composite as fillers for antistatic and anticorrosion coatings. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2008  相似文献   

11.
以苯胺作为导电聚合物单体,以普通高分子如醋酸纤维素作为成膜材料,以磷钨酸为掺杂剂制备二维聚苯胺/醋酸纤维素(PANI/CA)导电聚合物复合膜。利用红外和紫外光谱等测试手段对复合膜进行组成以及结构方面的表征。探索了导电聚合物复合膜制备的最佳工艺条件,并考察了复合膜的导电性。  相似文献   

12.
Polyaniline/nano‐SiO2 particle composites were prepared through ultrasonic irradiation. Polymerization of aniline was conducted under ultrasonic irradiation in the presence of two types of nano‐SiO2: porous nanosilica and spherical nanosilica. The stability of the colloid dispersion, UV–vis spectra, composition, interaction, conductivity, and other characteristics of the composites were examined. It was found that the aggregation of nano‐SiO2 could be reduced under ultrasonic irradiation and that nanoparticles were redispersed in the aqueous solution. The formed polyaniline deposited on the surface of the nanoparticle, which led to a core–shell structure. Two particle morphologies, threadlike aggregates with a few spherical nanoparticles for porous nanosilica and spherical particles with a few sandwichlike particles for spherical nanosilica, were observed. X‐ray photoelectron spectroscopy showed that for two types of composites the ratio of Si atoms to N atoms (Si:N) on the surface was much higher than that in the bulk. The UV–vis spectra of the diluted colloid dispersion of polyaniline/nano‐SiO2 composite particles were similar to those of the polyaniline system. Fourier transform infrared spectroscopy suggested strong interaction between polyaniline and nano‐SiO2. The conductivity of the polyaniline/porous nanosilica (23.1 wt % polyaniline) and polyaniline/spherical nanosilica (20.6 wt % polyaniline) composites was 2.9 and 0.2 S/cm, respectively. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 87: 1811–1817, 2003  相似文献   

13.
The nanothread of polyaniline (PANI) using ammonium persulphate ((NH4)2S2O8) as an oxidant was prepared. The solution is composed of 0.4 mol dm?3 aniline, 1.0 mol dm?3 hydrochloric acid, and different proportions ethanol. The resulting products were characterized using infrared spectroscopy, UV–vis spectra, transmission electron microscope, thermogravimetric analysis techniques, and X‐ray diffraction. The experimental results show that the content of ethanol has effects on the morphology of PANI, but the effects on the conductivity are not very obvious. When the volume ratio of ethanol to aniline is 1:2, the more uniform and regular PANI nanothread can be prepared. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 99: 1848–1853, 2006  相似文献   

14.
Polyaniline–clay nanocomposites were prepared by solid state polymerization of aniline chloride in the interlayer of montmorillonite through the use of persulfate of ammonium as oxidant. The proportion of aniline to clay and the molar ratio of oxidant to aniline are being varied. The analyse of UV visible and FTIR spectroscopy demonstrated that aniline has been polymerized to polyaniline (PANI) in its conducting emeraldine form. The conformation adopted by PANI chains in the clay interlayer depended on the molar ratio of aniline to montmorillonite. Thermogravimetric analysis of the nanocomposites suggested that polyaniline chains are more thermally stable than those of free polyaniline prepared by solid–solid reaction. The AC conductivity data of different synthesized nanocomposites were analyzed as a function of frequency. Low frequency conductivities of polyaniline/montmorillonite nanocomposites materials ranges from 0.18 to 5.6 × 10?3 S/cm. All characterization data were compared to those of free polyaniline that was synthesized using a solid–solid reaction.  相似文献   

15.
A polyaniline–TiO2 hybrid was coated on cotton fabric to make it electrically conductive. A One‐pot method of synthesis with acetic acid medium was used, in which TiCl4 was used as precursor. The oxidative polymerization of aniline adsorbed on TiO2 (anatase form) was performed in the presence of cotton fabric. Fabric crystallinity was least affected by the coatings, as confirmed by XRD analysis. FTIR studies revealed interactions between fiber and hybrid. The morphological study through SEM showed the uniform coating of hybrid over the fibers of the cotton fabric and AFM analysis revealed the rod‐like structure of the hybrid. The strength of the coated fabrics was assessed using abrasion tests. The electrical conductivity was determined using electrochemical impedance spectroscopy (EIS).The conductivity value varied with respect toTiO2 content and ranged in the order 10?4 to 102S/cm. The effect of atmospheric aging was assessed. A more durable conductivity was observed in hybrid‐coated fabric than pristine polyaniline‐coated fabric. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013  相似文献   

16.
Self‐doped poly(aniline‐co‐aminonaphthalene sulfonic acid) (PANI‐ANSA) was synthesized by the copolymerization of 5‐aminonaphthalene‐2‐sulfonic acid (ANSA) and aniline. Scanning electron microscopy and transmission electron microscopy showed that the morphology of PANI‐ANSA synthesized at a high molar ratio of aniline to ANSA was nanotubular, but at a low molar ratio, only a granular morphology formed. A possible formation mechanism for nanotubes was proposed. PANI‐ANSA had better thermal stability than HCl‐doped polyaniline; the highest onset decomposition temperature was as high as 340°C because of ? SO3H linked with the polymer backbone by a covalent bond. PANI‐ANSA was partially soluble in basic solutions, and its conductivity was between 10?2 and 10?4 S/cm, depending on the sulfonation degree. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 87: 1297–1301, 2003  相似文献   

17.
The effect of Cs+ ions added to the electrolyte for polyaniline films electrosynthesized in 0.1 m aniline/0.5m H2SO4 was investigated. Some properties of PANI films, such as the capacitance, the ohmic resistance and the charge-transfer resistance were obtained using electrochemical impedance spectroscopy. It was found that Cs+ ions used during PANI synthesis change its morphology, with a consequent increase in capacitance and conductivity, and a decrease in charge-transfer resistance.  相似文献   

18.
Electrocatalytic effects on electropolymerization of aniline were investigated. It was determined that surface catalysis by β‐PbO2 causes formation of higher amounts of polyaniline than catalysis by α‐PbO2 and Pb2+ ions. β‐PbO2 surfaces decreased the upper potential limit of aniline electropolymerization about 400 mV. The catalytic effect of PbO2 is highly dependent upon the crystal structure of PbO2. Dry conductivity values of polyaniline samples obtained under different conditions were also compared. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 87: 599–605, 2003  相似文献   

19.
Enzymatic synthesis of a water‐soluble, conducting polyaniline (PANI) was studied, using horseradish peroxidase as the biocatalyst and H2O2 as the initiator, in the presence of a poly(vinylsulfonic acid, sodium salt) (PVS) polyanion template. The effects of the buffer, concentration of H2O2, and the molar ratio of aniline to PVS on the polymerization were particularly investigated. The products were characterized by UV–vis/near‐IR and FTIR spectroscopy, thermogravimetric analysis, and four‐point probe conductivity measurement. The results showed that PVS could be chosen as a new template in the synthesis of PANI. The proper conditions of polymerization were obtained as follows: pH of the buffer was pH 4.0–5.0, the concentration of H2O2 was around 20 mM, and the molar ratio of PVS to aniline was 1–1.5. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 96: 814–817, 2005  相似文献   

20.
A series of novel soluble and thermoplastic polyurethane/polyaniline (TPU/PANI) composites doped with a compound acid, which was composed of an organic acid (p‐toluene sulfonic acid) and an inorganic acid (phosphoric acid), were successfully prepared by in situ polymerization. The effect of aniline (ANI) content, ratio of organic acid/inorganic acid, and different preparation methods on the conductivity of the TPU/PANI composites were investigated by using conductivity measurement. Lithium bisoxalato borate (LiBOB) was added to the prepared in situ TPU/PANI to coordinate with the ether oxygen groups originating from the soft molecular chains of TPU, and thus the conductivity of the composites was further enhanced. The molecular structure, thermal properties, and morphology of the TPU/PANI composites were studied by UV–visible spectroscopy, differential scanning calorimetry, and scanning electron microscopy, respectively. The results show that the in situ TPU/PANI composites doped with the compound acid can be easily dissolved in normal solvents such as dimethylformamide (DMF) and 1,4‐dioxane. The conductivity of the TPU/PANI composites increases with the increase of the ANI content, in the ANI content range of 0–20 wt %; however, the conductivity of the composites reduces with further increment of ANI content. The conductivity of the TPU/PANI composites prepared by in situ polymerization is about two orders of magnitude higher than that prepared by solution blending method. LiBOB can endow the in situ TPU/PANI composites with an ionic conductivity. The dependence of the conductivity on temperature is in good accordance with the Arrhenius equation in the temperature range of 20–80°C. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2010  相似文献   

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