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Preparation method of polyaniline nanometer fiber

A technology of nanofibers and polyaniline, applied in the field of preparation of polyaniline nanofibers, can solve the problems of limited electrode area, low synthesis output, expensive, etc., and achieve the effect of simple and easy operation, low cost and high production efficiency

Inactive Publication Date: 2013-11-27
DONGHUA UNIV
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  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Although the template-free method has achieved certain success in the preparation of polyaniline nanofibers, it also has some disadvantages. For example, a large amount of emulsifier is often used in the reaction process of the emulsion polymerization method, and the post-treatment process is cumbersome; and the most common interfacial polymerization method requires A large amount of organic solvent is used, and the synthesis yield is low. In addition to the irregularity of the prepared polyaniline nanofibers, the ultrasonic polymerization method also requires the use of more expensive equipment and is not suitable for large-scale production.
Although the electrochemical polymerization method [CN1958854A, CN101942090B] effectively controls the size and shape of nanofibers by selecting appropriate electrochemical parameters, this method is only suitable for small batches of one-dimensional conductive polymers due to limited electrode area.

Method used

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  • Preparation method of polyaniline nanometer fiber
  • Preparation method of polyaniline nanometer fiber
  • Preparation method of polyaniline nanometer fiber

Examples

Experimental program
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Effect test

Embodiment 1

[0027] Accurately weigh 0.2794g of aniline and 0.1712g of ammonium persulfate, and add them into two flasks containing 100ml of 1mol / L hydrochloric acid solution respectively. After fully dissolving, it was introduced into a reaction tube with an inner diameter of 1.25mm and a length of 100cm, and the reaction product was collected in a beaker filled with 5% acetone aqueous solution. Adjust the height difference between the liquid level in the flask and the end of the reaction tube (see figure 1 ), control the flow rate at 20ml / h. After the flow was completed, the beaker was left to stand at room temperature for 2 h. After repeated washing, high-speed centrifugation and drying of the reaction product, polyaniline nanofibers with a diameter of 45 ± 5 nm and a length of 700 ± 50 nm (see figure 2 ).

Embodiment 2

[0029] Accurately weigh 0.0931g of aniline and 0.0338g of potassium persulfate, and add them into two flasks containing 100ml of 1mol / L camphorsulfonic acid solution respectively. After fully dissolving, introduce it into a reaction tube with an inner diameter of 0.7mm and a length of 400cm, and collect the reaction product in a beaker filled with a mixed solution of 20% acetone and ethanol (the volume ratio of acetone and ethanol is 1:0.1). Adjust the height difference between the liquid level in the beaker and the end of the reaction tube to control the flow rate at 5ml / h. After the flow was completed, the beaker was left to stand at room temperature for 6 h. After repeated washing, high-speed centrifugation and drying of the reaction product, polyaniline nanofibers with a diameter of 35 ± 10 nm and a length of 1 μm ± 200 nm (see image 3 ).

Embodiment 3

[0031] Accurately weigh 1.8624g of aniline and 10.812g of ferric chloride, and add them into two flasks containing 100ml of 0.5mol / L hydrochloric acid solution respectively. After fully dissolving, introduce it into a reaction tube with an inner diameter of 2 mm and a length of 50 cm, and collect the reaction product in a beaker filled with 50% acetone and ethanol aqueous solution (the ratio of acetone and ethanol is 1:0.01). Adjust the height difference between the liquid level in the flask and the end of the reaction tube, and set the flow rate at 100ml / h. After the flow was completed, the beaker was allowed to stand at room temperature for 8 h. After repeated washing, high-speed centrifugation and drying of the reaction product, polyaniline nanofibers with a diameter of 50 ± 10 nm and a length of 300 ± 100 nm (see Figure 4 ).

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Abstract

The invention relates to a preparation method of a polyaniline nanometer fiber. The method comprises the following steps: dissolving a phenylamine monomer and a monomer initiator in acidic solutions containing dopants respectively; respectively loading the resulting solutions in a container A and a container B, wherein the liquid levels in the container A and the container B are consistent; introducing the solutions inside the container A and the container B into a reaction tube, controlling the free flow speeds of the reaction liquids inside the reaction tube, and collecting the reaction products by using a container C containing an inhibitor solution, wherein in the free flow process, the phenylamine is subjected to a polymerization reaction at room temperature or in an ice water environment, and the molar ratio of the phenylamine monomer to the monomer initiator is 1: (0.1-5); and after the flow is finished, causing the reaction products inside the container C to stand still, and then carrying out washing, centrifugation, and drying to obtain the polyaniline nanometer fiber. The preparation method provided by the invention is simple and easy to operate and low in cost; no template needs to be used; the whole process is mainly carried out in a water phase and tedious posttreatment is not needed; the preparation method is high in production efficiency, capable of realizing batch preparation and suitable for industrialized production.

Description

technical field [0001] The invention belongs to the field of preparation of nanofiber materials, in particular to a preparation method of polyaniline nanofibers. Background technique [0002] Because one-dimensional nanostructured polyaniline has different properties from ordinary polyaniline random particles, it has significant nano-size and space effects, especially its highly ordered aggregated structure greatly improves its carrier mobility. It plays an important role in the fabrication of interconnections and functional units of electronic, optoelectronic, electrochemical and electrical devices at the nanoscale, and has shown great applications in the fields of supercapacitors, biological and chemical sensors, electromagnetic shielding, and adsorption materials potential. In addition to electrospinning [CN100360725C, CN101967279A, CN101973713A], mechanical stretching and other physical methods for synthesizing nanostructured polyaniline, the synthesis of polyaniline ca...

Claims

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Application Information

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IPC IPC(8): C08G73/02
Inventor 秦宗益骆洁妮梁浜雷赵健云李涛
Owner DONGHUA UNIV
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