CN103063721A - Solid nitrite ion electrode based on conductive polyaniline and preparing method thereof - Google Patents

Solid nitrite ion electrode based on conductive polyaniline and preparing method thereof Download PDF

Info

Publication number
CN103063721A
CN103063721A CN2012105378169A CN201210537816A CN103063721A CN 103063721 A CN103063721 A CN 103063721A CN 2012105378169 A CN2012105378169 A CN 2012105378169A CN 201210537816 A CN201210537816 A CN 201210537816A CN 103063721 A CN103063721 A CN 103063721A
Authority
CN
China
Prior art keywords
nitrite ion
conductive polyaniline
electrode
electrically conductive
tinsel
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
CN2012105378169A
Other languages
Chinese (zh)
Other versions
CN103063721B (en
Inventor
叶瑛
黄元凤
丁茜
殷天雅
郑豪
潘依雯
李俊
陈雪刚
夏枚生
张海燕
刘舒婷
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Zhejiang University ZJU
Original Assignee
Zhejiang University ZJU
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Zhejiang University ZJU filed Critical Zhejiang University ZJU
Priority to CN201210537816.9A priority Critical patent/CN103063721B/en
Publication of CN103063721A publication Critical patent/CN103063721A/en
Application granted granted Critical
Publication of CN103063721B publication Critical patent/CN103063721B/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Landscapes

  • Electrodes For Compound Or Non-Metal Manufacture (AREA)
  • Investigating Or Analyzing Materials By The Use Of Fluid Adsorption Or Reactions (AREA)

Abstract

The invention discloses a solid nitrite ion electrode based on conductive polyaniline and a preparing method thereof. The solid nitrite ion electrode comprises a metal wire, the conductive polyaniline, soluble conductive polyaniline, nitrite ion sensitive film and a heat shrink tube, wherein a layer of the conductive polyaniline is electroplated on the surface of the lower portion of the metal wire, a layer of the soluble conductive polyaniline is wrapped on the outer surface of the conductive polyaniline, the nitrite ion sensitive film is wrapped on the outer surface of the soluble conductive polyaniline, and the heat shrink tube is wrapped on a portion located in the middle of the metal wire and with a distance greater than 0.5-1cm from the end portion of the nitrite ion sensitive film. The solid nitrite ion electrode based on the conductive polyaniline has the advantages of being high in mechanical strength, large in toughness, high in sensitivity, small in size, quick in detection response, low in detection limit, long in service life and the like. When matched with a solid reference electrode for use, the solid nitrite ion electrode based on the conductive polyaniline is applicable to on line detection and long-term in situ monitoring of nitrite ion content in seawater, aquaculture water, and chemistry or chemical industry water mediums.

Description

A kind of solid nitrite ion electrode based on electrically conductive polyaniline and preparation method thereof
Technical field
The present invention relates to the electrochemical detection technology, relate in particular to a kind of solid nitrite ion electrode based on electrically conductive polyaniline and preparation method thereof.
Background technology
The water body Nitrite Ion Content is the important parameter that carries out environmental evaluation, and for the activity of understanding organism in water, microorganism, and environmental pollution monitoring is significant.The commercial nitrite ion electrode that is used at present this type of purpose all belongs to liquid membrane electrode, and namely electrode interior need to fill electrolyte solution, i.e. and so-called " salt bridge ", its effect is the response signal that conduction detects between ion sensitive membrane and plain conductor.The major defect of liquid film type electrode comprises: volume more greatly, fragile, easily signal drift occurs, serviceable life is short.
Compare with traditional liquid film type electrode, solid electrode has that volume is little, intensity is high, and the comprehensive advantages such as long service life are suitable for natural water body, especially the long term monitoring of marine environment and online observation.The present invention is directed to this demand and proposed a kind of solid nitrite ion electrode based on electrically conductive polyaniline and preparation method thereof.
Summary of the invention
The objective of the invention is to overcome the deficiencies in the prior art, a kind of solid nitrite ion electrode based on electrically conductive polyaniline and preparation method thereof is provided.
The objective of the invention is to be achieved through the following technical solutions:
Solid nitrite ion electrode based on electrically conductive polyaniline comprises tinsel, electrically conductive polyaniline, fusible conductive polyaniline, nitrite ion sensitive membrane, heat-shrink tube, the tinsel lower surface is electroplated one deck electrically conductive polyaniline, outside surface at electrically conductive polyaniline coats one deck fusible conductive polyaniline, outside surface at fusible conductive polyaniline is coated with again the nitrite ion sensitive membrane, is coated with heat-shrink tube in the middle part of the tinsel and from the part outside more than nitrite ion sensitive membrane end 0.5-1 centimetre.
Described tinsel is Ag, Au, Pt, or the surface is coated with copper wire or the nickel wire of Ag, Au, Pt metal film.Described fusible conductive polyaniline be tinsel in the hydrochloric acid solution of aniline monomer, electroplate to form.Described fusible conductive polyaniline is that mol ratio is the aniline of 1:5~5:1 and the doped hydrochloride multipolymer of 2.5-dimethoxyaniline.
Step based on the preparation method of the solid nitrite ion electrode of electrically conductive polyaniline is as follows:
1) with length be 5~15 centimetres tinsel, surface and oil contaminant is removed in first ultrasonic cleaning in acetone soln, and oxide is removed in ultrasonic cleaning in 1~2M watery hydrochloric acid again, uses after the deionized water ultrasonic cleaning dry again;
2) aniline and hydrochloric acid are mixed with the aniline hydrochloride solution of 0.5~1M by the mol ratio of 1:1, perhaps with the aniline hydrochloride chip solid, are dissolved in the deionized water, make the aniline hydrochloride solution of 0.5~1M; Electroplate one deck electrically conductive polyaniline with cyclic voltammetry on top layer wiry by the CHI760D electrochemical workstation; Wherein, scanning current potential 0-0.45V, sweep velocity 50mV/s, sampling interval 1mV, sensitivity 10 -4A/V; Tinsel is done anode, and auxiliary electrode is the Pt electrode, and contrast electrode is commercial Ag/AgCl electrode; Three electrodes are inserted simultaneously in the aniline hydrochloride solution of 0.5~1M, continuous sweep 10 ~ 20 circulations, with anhydrous alcohol drip washing electrode, stand-by after the alcohol volatilization after plating is finished;
3) get 5 to 50 milligrams of aniline and 2, the doped hydrochloride multipolymer of 5-dimethoxyaniline, with N, dinethylformamide is that solvent is mixed with saturated solution, dip rapidly the N of soluble polyaniline with the electrode that is coated with electrically conductive polyaniline, the dinethylformamide saturated solution is inserted in the crucible that fills sand, dries 4~6 hours in 80~150 ℃ of baking ovens;
4) the nitrite ion carrier of Sigma company and film forming agent, plastifier, kation impedance agent are dissolved in the DMF, are mixed with mixed solution, it consists of by percentage to the quality:
Form A:
Nitrite ion carrier I 1.0%;
Four [3,5-two (trifluoromethyl) phenyl] potassium borate 0.3%;
2-nitrobenzene octyl ether 65.7%;
PVC 33.0% ;
Form B:
Nitrite ion carrier I 1.0%;
Di-n-octyl sebacate 66.0%;
PVC 33.0% ;
Form C:
Nitrite ion carrier II 1.0%;
Di-n-octyl sebacate 66.0%;
PVC 33.0% ;
5) dip mixed solution 1~3 time with the surperficial electrode that is coated with soluble polyaniline, be inserted on the polyfoam, placed the vacuum dryer vacuum drying 24 hours, until solvent obtains the nitrite ion sensitive membrane after volatilizing fully;
6) heat-shrink tube is coated in the middle part of the tinsel and from part more than nitrite ion sensitive membrane end 0.5-1 centimetre.
Exploring electrode volume of the present invention is little, highly sensitive, and probe response is fast, has very high physical strength and toughness, has good serviceability under condition of high voltage.Therefore be applicable to the nitrite ion content in seawater, breeding water and chemistry, the chemical industry aqueous medium is surveyed and long-term in-situ monitoring online, compare with traditional sampling analysis, both alleviated working strength, avoided the secondary pollution in the sampling process, improved again the real-time of data, reliability.
Description of drawings:
Fig. 1 is based on the structural representation of the solid nitrite ion electrode of electrically conductive polyaniline;
Among the figure: tinsel 1, electrically conductive polyaniline 2, fusible conductive polyaniline 3, nitrite ion sensitive membrane 4, heat-shrink tube 5.
Embodiment
Solid nitrite ion electrode based on electrically conductive polyaniline comprises tinsel 1, electrically conductive polyaniline 2, fusible conductive polyaniline 3, nitrite ion sensitive membrane 4, heat-shrink tube 5, tinsel 1 lower surface is electroplated one deck electrically conductive polyaniline 2, outside surface at electrically conductive polyaniline 2 coats one deck fusible conductive polyaniline 3, outside surface at fusible conductive polyaniline 3 is coated with again nitrite ion sensitive membrane 4, tinsel 1 middle part and be 0.5~1 centimetre away from nitrite ion sensitive membrane 4 ends more than the part outside be coated with heat-shrink tube 5.
Described tinsel 1 is Ag, Au, Pt, and its effect is that electrode surface is passed to detection circuit by the response signal that the nitrite ion carrier forms.The recommendation noble metal, the undesired signal that can avoid the dissolved constituent in tinsel self and the water body to form because of electrochemical reaction.Be to reduce cost, can use the surface to be coated with the copper wire, nickel wire of Ag, Au, Pt as electrode base material.
Described electrically conductive polyaniline 2 be tinsel 1 in the hydrochloric acid solution of aniline monomer, electroplate to form.Conductive polyaniline film 2 has good electric conductivity, and there is not obvious interlayer barrier in the electric current conduction between the two; In addition, conductive polyaniline film has changed surface nature wiry, has increased the affinity between the organic coating layer of it and follow-up formation.
Described fusible conductive polyaniline 3 is that mol ratio is the aniline of 1:5~5:1 and the doped hydrochloride multipolymer of 2.5-dimethoxyaniline.The doped hydrochloride multipolymer of aniline and 2,5-dimethoxyaniline can use commercial product, also can oneself be synthetic, and its chemical synthesis process is consistent with polyaniline, is the mixture replacing aniline of aniline and 2,5-dimethoxyaniline being pressed 5:1 to 1:5.
Use the doped hydrochloride multipolymer of aniline and 2,5-dimethoxyaniline to have triple effects: It has electric conductivity as electrically conductive polyaniline;
Figure DEST_PATH_IMAGE004
The plated conductive polyaniline composition of it and internal layer approaches, and chemical affinity is strong;
Figure DEST_PATH_IMAGE006
It and outermost layer nitrite ion carrier can both be dissolved in N, dinethylformamide, thereby in the process that coats the nitrite ion carrier, can be partly dissolved, be made nitrite ion sensitive membrane and soluble polyaniline close contact, conductive impairment between eliminating layer.
Step based on the preparation method of the solid nitrite ion electrode of electrically conductive polyaniline is as follows:
1) with length be 5~15 centimetres tinsel 1, surface and oil contaminant is removed in first ultrasonic cleaning in acetone soln, and oxide is removed in ultrasonic cleaning in 1~2M watery hydrochloric acid again, uses after the deionized water ultrasonic cleaning dry again;
2) aniline and hydrochloric acid are mixed with the aniline hydrochloride solution of 0.5~1M by the mol ratio of 1:1, perhaps with the aniline hydrochloride chip solid, are dissolved in the deionized water, make the aniline hydrochloride solution of 0.5~1M; Electroplate one deck electrically conductive polyaniline 2 with cyclic voltammetry on the top layer of tinsel 1 by the CHI760D electrochemical workstation; Wherein, scanning current potential 0-0.45V, sweep velocity 50mV/s, sampling interval 1mV, sensitivity 10 -4A/V; Tinsel 1 is done anode, and auxiliary electrode is the Pt electrode, and contrast electrode is commercial Ag/AgCl electrode; Three electrodes are inserted simultaneously in the aniline hydrochloride solution of 0.5~1M, continuous sweep 10 ~ 20 circulations, with anhydrous alcohol drip washing electrode, stand-by after the alcohol volatilization after plating is finished;
3) get 5 to 50 milligrams of aniline and 2, the doped hydrochloride multipolymer of 5-dimethoxyaniline, with N, dinethylformamide is that solvent is mixed with saturated solution, dip rapidly the N of soluble polyaniline with the electrode that is coated with electrically conductive polyaniline 2, the dinethylformamide saturated solution is inserted in the crucible that fills sand, dries 4~6 hours in 80~150 ℃ of baking ovens;
4) the nitrite ion carrier of Sigma company and film forming agent, plastifier, kation impedance agent are dissolved in the DMF, are mixed with mixed solution, it consists of by percentage to the quality:
Form A:
Nitrite ion carrier I 1.0%;
Four [3,5-two (trifluoromethyl) phenyl] potassium borate 0.3%;
2-nitrobenzene octyl ether 65.7%;
PVC 33.0% ;
Form B:
Nitrite ion carrier I 1.0%;
Di-n-octyl sebacate 66.0%;
PVC 33.0% ;
Form C:
Nitrite ion carrier II 1.0%;
Di-n-octyl sebacate 66.0%;
PVC 33.0% ;
5) dip mixed solution 1~3 time with the surperficial electrode that is coated with soluble polyaniline 3, be inserted on the polyfoam, placed the vacuum dryer vacuum drying 24 hours, until solvent obtains nitrite ion sensitive membrane 4 after volatilizing fully; Vacuum drying under the recommendation normal temperature avoids using hyperthermia drying, is in order better to protect the activity of nitrite ion sensitive membrane;
6) heat-shrink tube 5 is coated on tinsel 1 middle part and be part 0.5~1 centimetre away from nitrite ion sensitive membrane 4 ends more than.
Embodiment 1
1) with length be 10 centimetres tinsel 1, surface and oil contaminant is removed in first ultrasonic cleaning in acetone soln, and oxide is removed in ultrasonic cleaning in 1M watery hydrochloric acid again, uses after the deionized water ultrasonic cleaning dry again;
2) take by weighing 1.9439g commodity aniline hydrochloride chip solid, be dissolved in the 15ml deionized water, make the aniline hydrochloride solution of 1M; Electroplate one deck electrically conductive polyaniline 2 with cyclic voltammetry on the top layer of tinsel 1 by the CHI760D electrochemical workstation.
Experiment parameter is: scanning current potential 0-0.45V, sweep velocity 50mV/s, sampling interval 1mV, sensitivity 10 -4A/V; Tinsel 1 is done anode, and auxiliary electrode is the Pt electrode, and contrast electrode is commercial Ag/AgCl electrode; Three electrodes are inserted simultaneously in the aniline hydrochloride solution of 1M, continuous sweep 20 circulations, with anhydrous alcohol drip washing electrode, stand-by after the alcohol volatilization after plating is finished;
3) take by weighing 35 milligrams of aniline and 2, the doped hydrochloride multipolymer of 5-dimethoxyaniline (mol ratio of the two is 5:1), be dissolved in and be mixed with saturated solution among the 10mlDMF, the electrode that is coated with electrically conductive polyaniline 2 with the surface dips rapidly the N of soluble polyaniline, dinethylformamide (DMF) saturated solution, be inserted in the crucible that fills sand, oven dry is 6 hours in 80 ℃ of baking ovens;
4) nitrite ion carrier and attached component thereof are dissolved among the DMF according to forming A, are mixed with mixed solution, its composition A is by percentage to the quality:
Nitrite ion carrier (Nitrite ionophore I) 1.0%,
Four [3,5-two (trifluoromethyl) phenyl] potassium borate,
(Potassium tetrakis [3,5- bis (trifluoromethyl) phenyl ])0.3% ,
2-nitrobenzene octyl ether (2-Nitrophenyl octyl ether) 65.7%,
PVC(Poly(vinyl chloride) high molecular weight)33.0% ;
5) dip fast mixed solution with the surperficial electrode that is coated with soluble polyaniline 3, be inserted on the polyfoam, placed the vacuum dryer vacuum drying 24 hours, until solvent obtains nitrite ion sensitive membrane 4 after volatilizing fully;
6) heat-shrink tube 5 is coated on tinsel 1 middle part and be part 0.5 centimetre away from nitrite ion sensitive membrane 4 ends more than.
Embodiment 2
1) with length be 8 centimetres tinsel 1, surface and oil contaminant is removed in first ultrasonic cleaning in acetone soln, and oxide is removed in ultrasonic cleaning in 2M watery hydrochloric acid again, uses after the deionized water ultrasonic cleaning dry again;
2) take by weighing respectively 10.1388g hydrochloric acid, 9.313g aniline, in the 100ml volumetric flask, add water to the solution that scale namely gets hydrochloric acid: aniline=1M:1M; Electroplate one deck electrically conductive polyaniline 2 with cyclic voltammetry on the top layer of tinsel 1 by the CHI760D electrochemical workstation.
Experiment parameter is: scanning current potential 0-0.45V, sweep velocity 50mV/s, sampling interval 1mV, sensitivity 10 -4A/V; Tinsel 1 is done anode, and auxiliary electrode is the Pt electrode, and contrast electrode is commercial Ag/AgCl electrode; Three electrodes are inserted simultaneously in the aniline hydrochloride solution of 1M, continuous sweep 20 circulations, with anhydrous alcohol drip washing electrode, stand-by after the alcohol volatilization after plating is finished;
3) take by weighing 35 milligrams of aniline and 2, the doped hydrochloride multipolymer of 5-dimethoxyaniline (mol ratio of the two is 1:1), be dissolved in and be mixed with saturated solution among the 10mlDMF, the electrode that is coated with electrically conductive polyaniline 2 with the surface dips rapidly the DMF saturated solution of soluble polyaniline, be inserted in the crucible that fills sand, oven dry is 5 hours in 100 ℃ of baking ovens;
4) nitrite ion carrier and attached component thereof are dissolved among the DMF according to forming A, are mixed with mixed solution, its composition A is by percentage to the quality:
Nitrite ion carrier (Nitrite ionophore I) 1.0%,
Four [3,5-two (trifluoromethyl) phenyl] potassium borate,
(Potassium tetrakis [3,5- bis (trifluoromethyl) phenyl ])0.3% ,
2-nitrobenzene octyl ether (2-Nitrophenyl octyl ether) 65.7%,
PVC(Poly(vinyl chloride) high molecular weight)33.0% ;
5) dip fast mixed solution with the surperficial electrode that is coated with soluble polyaniline 3, repeat once, be inserted on the polyfoam, placed the vacuum dryer vacuum drying 24 hours, until solvent obtains nitrite ion sensitive membrane 4 after volatilizing fully;
6) heat-shrink tube 5 is coated on tinsel 1 middle part and be part 0.8 centimetre away from nitrite ion sensitive membrane 4 ends more than.
Embodiment 3
1) with length be 10 centimetres tinsel 1, surface and oil contaminant is removed in first ultrasonic cleaning in acetone soln, and oxide is removed in ultrasonic cleaning in 1M watery hydrochloric acid again, uses after the deionized water ultrasonic cleaning dry again;
2) take by weighing 0.9720g commodity aniline hydrochloride chip solid, be dissolved in the 15ml deionized water, make the aniline hydrochloride solution of 0.5M; Electroplate one deck electrically conductive polyaniline 2 with cyclic voltammetry on the top layer of tinsel 1 by the CHI760D electrochemical workstation;
Experiment parameter is: scanning current potential 0-0.45V, sweep velocity 50mV/s, sampling interval 1mV, sensitivity 10 -4A/V; Tinsel 1 is done anode, and auxiliary electrode is the Pt electrode, and contrast electrode is commercial Ag/AgCl electrode; Three electrodes are inserted simultaneously in the aniline hydrochloride solution of 1M, continuous sweep 20 circulations, with anhydrous alcohol drip washing electrode, stand-by after the alcohol volatilization after plating is finished;
3) take by weighing 35 milligrams of aniline and 2, the doped hydrochloride multipolymer of 5-dimethoxyaniline (mol ratio of the two is 5:1), be dissolved in and be mixed with saturated solution among the 10mlDMF, the electrode that is coated with electrically conductive polyaniline 2 with the surface dips rapidly the DMF saturated solution of soluble polyaniline, be inserted in the crucible that fills sand, oven dry is 4 hours in 150 ℃ of baking ovens;
4) nitrite ion carrier and attached component thereof are dissolved among the DMF according to forming B, are mixed with mixed solution, its composition B is by percentage to the quality:
Nitrite ion carrier (Nitrite ionophore I) 1.0%,
Di-n-octyl sebacate (Bis (2-ethylhexyl) sebacate) 66.0%,
PVC(Poly(vinyl chloride) high molecular weight)33.0% ;
5) dip fast mixed solution with the surperficial electrode that is coated with soluble polyaniline 3, repeat twice, be inserted on the polyfoam, placed the vacuum dryer vacuum drying 24 hours, until solvent obtains nitrite ion sensitive membrane 4 after volatilizing fully;
6) heat-shrink tube 5 is coated on tinsel 1 middle part and be part 1 centimetre away from nitrite ion sensitive membrane 4 ends more than.
Embodiment 4
1) with length be 15 centimetres tinsel 1, surface and oil contaminant is removed in first ultrasonic cleaning in acetone soln, and oxide is removed in ultrasonic cleaning in 1M watery hydrochloric acid again, uses after the deionized water ultrasonic cleaning dry again;
2) take by weighing 1.9439g commodity aniline hydrochloride chip solid, be dissolved in the 15ml deionized water, make the aniline hydrochloride solution of 1M; Electroplate one deck electrically conductive polyaniline 2 with cyclic voltammetry on the top layer of tinsel 1 by the CHI760D electrochemical workstation;
Experiment parameter is: scanning current potential 0-0.45V, sweep velocity 50mV/s, sampling interval 1mV, sensitivity 10 -4A/V; Tinsel 1 is done anode, and auxiliary electrode is the Pt electrode, and contrast electrode is commercial Ag/AgCl electrode; Three electrodes are inserted simultaneously in the aniline hydrochloride solution of 1M, continuous sweep 20 circulations, with anhydrous alcohol drip washing electrode, stand-by after the alcohol volatilization after plating is finished;
3) take by weighing 35 milligrams of aniline and 2, the doped hydrochloride multipolymer of 5-dimethoxyaniline (mol ratio of the two is 1:5), be dissolved in and be mixed with saturated solution among the 10mlDMF, the electrode that is coated with electrically conductive polyaniline 2 with the surface dips rapidly the DMF saturated solution of soluble polyaniline, be inserted in the crucible that fills sand, oven dry is 4 hours in 150 ℃ of baking ovens;
4) nitrite ion carrier and attached component thereof are dissolved among the DMF according to forming C, are mixed with mixed solution, its composition C is by percentage to the quality:
Nitrite ion carrier (Nitrite ionophore II) 1.0%,
Di-n-octyl sebacate (Bis (2-ethylhexyl) sebacate) 66.0%,
PVC(Poly(vinyl chloride) high molecular weight)33.0% ;
5) dip fast mixed solution with the surperficial electrode that is coated with soluble polyaniline 3, repeat once, be inserted on the polyfoam, placed the vacuum dryer vacuum drying 24 hours, until solvent obtains nitrite ion sensitive membrane 4 after volatilizing fully;
6) heat-shrink tube 5 is coated on tinsel 1 middle part and be part 0.5 centimetre away from nitrite ion sensitive membrane 4 ends more than.
Embodiment 5
The solid nitrite ion is selected the demarcation of electrode,
The used mother liquor of preparation nitrite ion standard solution is the sodium nitrite solution of the 0.1M of Sigma company production, and used thinning agent is deionized water.
Pipette 10ml10 -1The sodium nitrite solution of M is diluted to 100ml with deionized water, makes 10 -2The sodium nitrite solution of M, the dilution preparation 10 successively -3M, 10 -4M, 10 -5M, 10 -6The sodium nitrite solution of M.
Select electrode as working electrode take the self-control nitrite ion, commodity Ag/AgCl electrode is contrast electrode, respectively working electrode and contrast electrode are connected to the CHI760D electrochemical workstation, the response electric signal from high concentration toward the low concentration sequentially determining, according to response signal intensity and concentration relationship mapping, the two linear relationship slope is between 57.2 ~ 60.4, and meeting can Si Tedinglv.

Claims (5)

1. solid nitrite ion electrode based on electrically conductive polyaniline, it is characterized in that comprising tinsel (1), electrically conductive polyaniline (2), fusible conductive polyaniline (3), nitrite ion sensitive membrane (4), heat-shrink tube (5), tinsel (1) lower surface is electroplated one deck electrically conductive polyaniline (2), outside surface at electrically conductive polyaniline (2) coats one deck fusible conductive polyaniline (3), outside surface at fusible conductive polyaniline (3) is coated with again nitrite ion sensitive membrane (4), is coated with heat-shrink tube (5) in the middle part of the tinsel (1) and be 0.5~1 centimetre away from nitrite ion sensitive membrane (4) end more than outside the part.
2. a kind of solid nitrite ion electrode based on electrically conductive polyaniline according to claim 1 is characterized in that, described tinsel (1) is Ag, Au, Pt, or the surface is coated with copper wire or the nickel wire of Ag, Au, Pt metal film.
3. a kind of solid nitrite ion electrode based on electrically conductive polyaniline according to claim 1 is characterized in that, described electrically conductive polyaniline (2) is that tinsel (1) is electroplated formation in the hydrochloric acid solution of aniline monomer.
4. a kind of solid nitrite ion electrode based on electrically conductive polyaniline according to claim 1, it is characterized in that, described fusible conductive polyaniline (3) is that mol ratio is the aniline of 1:5~5:1 and the doped hydrochloride multipolymer of 2.5-dimethoxyaniline.
5. preparation method based on the solid nitrite ion electrode of electrically conductive polyaniline is characterized in that its step is as follows:
1) with length be 5~15 centimetres tinsel (1), surface and oil contaminant is removed in first ultrasonic cleaning in acetone soln, and oxide is removed in ultrasonic cleaning in 1~2M watery hydrochloric acid again, uses after the deionized water ultrasonic cleaning dry again;
2) aniline and hydrochloric acid are mixed with the aniline hydrochloride solution of 0.5~1M by the mol ratio of 1:1, perhaps with the aniline hydrochloride chip solid, are dissolved in the deionized water, make the aniline hydrochloride solution of 0.5~1M; Electroplate one deck electrically conductive polyaniline (2) with cyclic voltammetry on the top layer of tinsel (1) by the CHI760D electrochemical workstation; Wherein, scanning current potential 0-0.45V, sweep velocity 50mV/s, sampling interval 1mV, sensitivity 10 -4A/V; Tinsel (1) is done anode, and auxiliary electrode is the Pt electrode, and contrast electrode is commercial Ag/AgCl electrode; Three electrodes are inserted simultaneously in the aniline hydrochloride solution of 0.5~1M, continuous sweep 10 ~ 20 circulations, with anhydrous alcohol drip washing electrode, stand-by after the alcohol volatilization after plating is finished;
3) get 5 to 50 milligrams of aniline and 2, the doped hydrochloride multipolymer of 5-dimethoxyaniline, with N, dinethylformamide is that solvent is mixed with saturated solution, dip rapidly the N of soluble polyaniline with the electrode that is coated with electrically conductive polyaniline (2), the dinethylformamide saturated solution is inserted in the crucible that fills sand, dries 4~6 hours in 80~150 ℃ of baking ovens;
4) the nitrite ion carrier of Sigma company and film forming agent, plastifier, kation impedance agent are dissolved in the DMF, are mixed with mixed solution, it consists of by percentage to the quality:
Form A:
Nitrite ion carrier I 1.0%;
Four [3,5-two (trifluoromethyl) phenyl] potassium borate 0.3%;
2-nitrobenzene octyl ether 65.7%;
PVC 33.0% ;
Form B:
Nitrite ion carrier I 1.0%;
Di-n-octyl sebacate 66.0%;
PVC 33.0% ;
Form C:
Nitrite ion carrier II 1.0%;
Di-n-octyl sebacate 66.0%;
PVC 33.0% ;
5) electrode that is coated with soluble polyaniline (3) with the surface dips mixed solution 1~3 time, is inserted on the polyfoam, places the vacuum dryer vacuum drying 24 hours, until solvent obtains nitrite ion sensitive membrane (4) after volatilizing fully;
6) heat-shrink tube (5) is coated on tinsel (1) middle part and be part 0.5~1 centimetre away from nitrite ion sensitive membrane (4) end more than.
CN201210537816.9A 2012-12-13 2012-12-13 Solid nitrite ion electrode based on conductive polyaniline and preparing method thereof Expired - Fee Related CN103063721B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201210537816.9A CN103063721B (en) 2012-12-13 2012-12-13 Solid nitrite ion electrode based on conductive polyaniline and preparing method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201210537816.9A CN103063721B (en) 2012-12-13 2012-12-13 Solid nitrite ion electrode based on conductive polyaniline and preparing method thereof

Publications (2)

Publication Number Publication Date
CN103063721A true CN103063721A (en) 2013-04-24
CN103063721B CN103063721B (en) 2014-10-15

Family

ID=48106433

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201210537816.9A Expired - Fee Related CN103063721B (en) 2012-12-13 2012-12-13 Solid nitrite ion electrode based on conductive polyaniline and preparing method thereof

Country Status (1)

Country Link
CN (1) CN103063721B (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103675068A (en) * 2013-03-28 2014-03-26 浙江大学 Bismuth nitrate oxide based solid nitrate electrode and preparation method thereof
CN105606678A (en) * 2015-09-08 2016-05-25 浙江大学 Doped polyaniline based solid acid radical electrode and preparation method thereof

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1667020A (en) * 2005-01-10 2005-09-14 厦门大学 Process for synthesizing electron donor substituted polyaniline derivatives
CN101077913A (en) * 2006-05-23 2007-11-28 中国科学院化学研究所 High obstructive polyaniline composite film and its preparation method and use
CN101435793A (en) * 2008-12-19 2009-05-20 西安建筑科技大学 Nitrite ionic selectivity micro-electrode and preparing method thereof
CN102156157A (en) * 2011-01-10 2011-08-17 浙江大学 All-solid-state carbonate ion selective electrode and manufacture method of all-solid-state carbonate ion selective electrode
CN102645461A (en) * 2012-03-31 2012-08-22 无锡百灵传感技术有限公司 Preparation method of electrochemical sensor based on polyaniline nanofiber

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1667020A (en) * 2005-01-10 2005-09-14 厦门大学 Process for synthesizing electron donor substituted polyaniline derivatives
CN101077913A (en) * 2006-05-23 2007-11-28 中国科学院化学研究所 High obstructive polyaniline composite film and its preparation method and use
CN101435793A (en) * 2008-12-19 2009-05-20 西安建筑科技大学 Nitrite ionic selectivity micro-electrode and preparing method thereof
CN102156157A (en) * 2011-01-10 2011-08-17 浙江大学 All-solid-state carbonate ion selective electrode and manufacture method of all-solid-state carbonate ion selective electrode
CN102645461A (en) * 2012-03-31 2012-08-22 无锡百灵传感技术有限公司 Preparation method of electrochemical sensor based on polyaniline nanofiber

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103675068A (en) * 2013-03-28 2014-03-26 浙江大学 Bismuth nitrate oxide based solid nitrate electrode and preparation method thereof
CN103675068B (en) * 2013-03-28 2015-10-21 浙江大学 A kind of solid nitric acid root electrode based on nitric acid oxidation bismuth and preparation method thereof
CN105606678A (en) * 2015-09-08 2016-05-25 浙江大学 Doped polyaniline based solid acid radical electrode and preparation method thereof

Also Published As

Publication number Publication date
CN103063721B (en) 2014-10-15

Similar Documents

Publication Publication Date Title
CN103675068B (en) A kind of solid nitric acid root electrode based on nitric acid oxidation bismuth and preparation method thereof
Wagner et al. Durable PEDOT: PSS films obtained from modified water-based inks for electrochemical sensors
CN103063724B (en) Solid carbonate ion electrode based on conductive polyaniline and preparing method thereof
CN105717174A (en) Electrochemical detection method for detecting trace heavy metal ions in water with modified graphene oxide composite modified electrode
CN108982626B (en) Nano electrochemical enzyme sensor for detecting trichloroacetic acid or sodium nitrite and preparation method and application thereof
Wang et al. Simultaneous detection of copper, lead and zinc on tin film/gold nanoparticles/gold microelectrode by square wave stripping voltammetry
CN103063718B (en) Solid nitrate ion electrode based on conductive polyaniline and preparing method thereof
Zeng et al. Improving the stability of Pb2+ ion-selective electrodes by using 3D polyaniline nanowire arrays as the inner solid-contact transducer
WO2010076717A1 (en) Ion-selective solid contact microelectrode and its production method
Dueraning et al. An environmental friendly electrode and extended cathodic potential window for anodic stripping voltammetry of zinc detection
CN103063723B (en) Solid hydrogen ion concentration electrode based on conductive polyaniline and preparing method thereof
CN103336044A (en) All solid-state ion selective electrode and preparation method and application thereof
Xu et al. A miniature all-solid-state calcium electrode applied to in situ seawater measurement
CN103063725B (en) Solid ammonium ion electrode based on conductive polyaniline and preparing method thereof
Jiang et al. A solid-contact Pb2+-selective electrode based on a hydrophobic polyaniline microfiber film as the ion-to-electron transducer
KR101608584B1 (en) Graphene thin film obtained from electrochemical reduction of hydroxyl groupenriched graphene oxide and method for detecting uric acid using the same
CN103063721B (en) Solid nitrite ion electrode based on conductive polyaniline and preparing method thereof
CN103063722B (en) Solid calcium ion electrode based on conductive polyaniline and preparing method thereof
CN105606678B (en) A kind of solid acid group electrode and preparation method thereof based on doped polyaniline
Zhang et al. Electrochemical behaviors of roxithromycin at poly (3, 4-ethylenedioxythiophene) modified gold electrode and its electrochemical determination
CN114646681B (en) Visual detection method of solid contact type ion selective electrode
Faridbod et al. Conducting polymer all solid state potentiometric sensor for the tramadol assay
CN109991293B (en) High-flexibility full-solid pH selective electrode and preparation method thereof
CN109254065A (en) A kind of application of silica/poly- furfural modified electrode and preparation method thereof and detection lead cadmium ion
CN102590303B (en) Anti-freezing Ag/AgCl reference electrode and preparation method thereof

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant
CF01 Termination of patent right due to non-payment of annual fee
CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20141015

Termination date: 20161213