CN103063718A - Solid nitrate ion electrode based on conductive polyaniline and preparing method thereof - Google Patents
Solid nitrate ion electrode based on conductive polyaniline and preparing method thereof Download PDFInfo
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- CN103063718A CN103063718A CN2012105382499A CN201210538249A CN103063718A CN 103063718 A CN103063718 A CN 103063718A CN 2012105382499 A CN2012105382499 A CN 2012105382499A CN 201210538249 A CN201210538249 A CN 201210538249A CN 103063718 A CN103063718 A CN 103063718A
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Abstract
The invention discloses a solid nitrate ion electrode based on conductive polyaniline and a preparing method thereof. The solid nitrate ion electrode comprises a metal wire, the conductive polyaniline, soluble conductive polyaniline, nitrate 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 nitrate 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 nitrate ion sensitive film. The solid nitrate 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 nitrate ion electrode based on the conductive polyaniline is applicable to on line detection and long-term in situ monitoring of nitrate ion content in seawater, aquaculture water, and chemistry or chemical industry water mediums.
Description
Technical field
The present invention relates to the electrochemical detection technology, relate in particular to a kind of solid nitric acid radical ion electrode based on electrically conductive polyaniline and preparation method thereof.
Background technology
Nitrate ion content is the important parameter that carries out environmental evaluation in the water body, and for the activity of understanding organism in water, microorganism, and environmental pollution monitoring is significant.The commercial nitrate 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 nitric acid radical 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 nitric acid radical 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 nitric acid radical ion electrode based on electrically conductive polyaniline comprises tinsel, electrically conductive polyaniline, fusible conductive polyaniline, nitrate 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 nitrate ion sensitive membrane, is coated with heat-shrink tube in the middle part of the tinsel and be 0.5～1 centimetre away from nitrate ion sensitive membrane end more than outside the part.
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 nitric acid radical 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 nitrate ion carrier of Sigma company and film forming agent, plastifier, kation impedance agent are dissolved in the DMF, are mixed with mixed solution, its composition is respectively by percentage to the quality:
Form A:
Nitrate ion carrier V 1.0%;
Dotriacontyl ammonio methacrylate 0.6%;
PVC 32.8% ；
2-nitrobenzene octyl ether 65.6%;
Form B:
Nitrate ion carrier V 6.0%;
PVC 29.0% ；
2-nitrobenzene octyl ether 65.0%;
Form C:
Nitrate ion carrier V 4.0%;
PVC 32.0% ；
Di-n-octyl sebacate 64.0%;
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 nitrate ion sensitive membrane after volatilizing fully;
6) heat-shrink tube is coated on tinsel middle part and be part 0.5～1 centimetre away from nitrate ion sensitive membrane end more than.
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 nitrate 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 schematic diagram of the solid nitric acid radical ion electrode structure of electrically conductive polyaniline;
Among the figure: tinsel 1, electrically conductive polyaniline 2, fusible conductive polyaniline 3, nitrate ion sensitive membrane 4, heat-shrink tube 5.
Embodiment
Solid nitric acid radical ion electrode based on electrically conductive polyaniline comprises tinsel 1, electrically conductive polyaniline 2, fusible conductive polyaniline 3, nitrate 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 nitrate ion sensitive membrane 4, tinsel 1 middle part and be 0.5～1 centimetre away from nitrate 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 nitrate 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;
The plated conductive polyaniline composition of it and internal layer approaches, and chemical affinity is strong;
It and outermost layer nitrate ion carrier can both be dissolved in DMF, thereby can be partly dissolved in the process that coats the nitrate ion carrier, make nitrate ion sensitive membrane and soluble polyaniline close contact, conductive impairment between eliminating layer.
Step based on the preparation method of the solid nitric acid radical 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 nitrate ion carrier of Sigma company and film forming agent, plastifier, kation impedance agent are dissolved in the DMF, are mixed with mixed solution, its composition is respectively by percentage to the quality:
Form A:
Nitrate ion carrier V 1.0%;
Dotriacontyl ammonio methacrylate 0.6%;
PVC 32.8% ；
2-nitrobenzene octyl ether 65.6%;
Form B:
Nitrate ion carrier V 6.0%;
PVC 29.0% ；
2-nitrobenzene octyl ether 65.0%;
Form C:
Nitrate ion carrier V 4.0%;
PVC 32.0% ；
Di-n-octyl sebacate 64.0%;
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 nitrate 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 nitrate ion sensitive membrane;
6) heat-shrink tube 5 is coated on tinsel 1 middle part and be part 0.5～1 centimetre away from nitrate ion sensitive membrane 4 ends more than.
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) nitrate 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:
Nitrate ion carrier (Nitrate ionophore V) 1.0%,
Dotriacontyl ammonio methacrylate (Tridodecylmethyl ammonium chloride) 0.6%,
PVC(Poly(vinyl chloride) high molecular weight)32.8% ，
2-nitrobenzene octyl ether (2-Nitrophenyl octyl ether) 65.6%;
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 nitrate 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 nitrate ion sensitive membrane 4 ends more than.
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) nitrate 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:
Nitrate ion carrier (Nitrate ionophore V) 1.0%,
Dotriacontyl ammonio methacrylate (Tridodecylmethyl ammonium chloride) 0.6%,
PVC(Poly(vinyl chloride) high molecular weight)32.8% ，
2-nitrobenzene octyl ether (2-Nitrophenyl octyl ether) 65.6%;
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 nitrate 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 nitrate ion sensitive membrane 4 ends more than.
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) nitrate 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:
Nitrate ion carrier (Nitrate ionophore V) 6.0%,
PVC(Poly(vinyl chloride) high molecular weight)29.0% ，
2-nitrobenzene octyl ether (2-Nitrophenyl octyl ether) 65.0%;
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 nitrate 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 nitrate ion sensitive membrane 4 ends more than.
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) nitrate 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:
Nitrate ion carrier (Nitrate ionophore V) 4.0%,
PVC(Poly(vinyl chloride) high molecular weight)32.0% ，
Di-n-octyl sebacate (Bis (2-ethylhexyl) sebacate) 64%;
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 nitrate 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 nitrate ion sensitive membrane 4 ends more than.
The solid nitric acid radical ion is selected the demarcation of electrode,
The used mother liquor of preparation nitrate ion standard solution is the 0.1M nitrate ion standard solution that Sigma company produces, and used thinning agent is deionized water.
Pipette 10ml10
-1The nitrate ion standard solution of M is diluted to 100ml with deionized water, makes 10
-2The nitrate ion solution of M, the dilution preparation 10 successively
-3M, 10
-4M, 10
-5M, 10
-6The nitrate ion solution of M.
Take the self-control Nitrate Ion Selective Electrode as working electrode, 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 55.1 ~ 59.0, and meeting can Si Tedinglv.
Claims (5)
1. solid nitric acid radical ion electrode based on electrically conductive polyaniline, it is characterized in that comprising tinsel (1), electrically conductive polyaniline (2), fusible conductive polyaniline (3), nitrate 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 nitrate 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 nitrate ion sensitive membrane (4) end more than outside the part.
2. a kind of solid nitric acid radical 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 nitric acid radical 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 nitric acid radical ion electrode based on electrically conductive polyaniline according to claim 1 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 nitric acid radical 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 nitrate ion carrier of Sigma company and film forming agent, plastifier, kation impedance agent are dissolved in the DMF, are mixed with mixed solution, its composition is respectively by percentage to the quality:
Form A:
Nitrate ion carrier V 1.0%;
Dotriacontyl ammonio methacrylate 0.6%;
PVC 32.8% ；
2-nitrobenzene octyl ether 65.6%;
Form B:
Nitrate ion carrier V 6.0%;
PVC 29.0% ；
2-nitrobenzene octyl ether 65.0%;
Form C:
Nitrate ion carrier V 4.0%;
PVC 32.0% ；
Di-n-octyl sebacate 64.0%;
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 nitrate 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 nitrate ion sensitive membrane (4) end more than.
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Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103293205A (en) * | 2013-06-08 | 2013-09-11 | 江南大学 | Preparation method of full-solid ion selective electrode based on bilayer membrane structure |
| 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 |
| CN106066354A (en) * | 2016-05-24 | 2016-11-02 | 浙江大学 | Nitrate ion electrode with polynitrobenzene amine as sensitive membrane and preparation method thereof |
Citations (3)
| 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 |
| CN201352210Y (en) * | 2008-12-25 | 2009-11-25 | 西安建筑科技大学 | Nitrate ion selective microelectrode |
| 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 |
-
2012
- 2012-12-13 CN CN201210538249.9A patent/CN103063718B/en not_active Expired - Fee Related
Patent Citations (3)
| 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 |
| CN201352210Y (en) * | 2008-12-25 | 2009-11-25 | 西安建筑科技大学 | Nitrate ion selective microelectrode |
| 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 |
Non-Patent Citations (4)
| Title |
|---|
| J. E. W. DAVIES ET AL: "Nitrate Ion Selective Electrodes Based on Poly(viny1 chloride) Matrix Membranes", 《ANALYST》 * |
| TOM LINDFORS ET AL: "All-solid-state calcium-selective electrode prepared of soluble electrically conducting polyaniline and di(2-ethylhexyl)phosphate with tetraoctylammonium chloride as cationic additive", 《ANALYTICA CHIMICA ACTA》 * |
| 余晓栋 等: "基于掺杂聚吡咯的硝酸根离子选择性电极", 《传感器与微系统》 * |
| 黄美荣 等: "导电聚合物构建的高性能固态离子选择电极", 《分析化学评述与进展》 * |
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| CN105606678A (en) * | 2015-09-08 | 2016-05-25 | 浙江大学 | Doped polyaniline based solid acid radical electrode and preparation method thereof |
| CN106066354A (en) * | 2016-05-24 | 2016-11-02 | 浙江大学 | Nitrate ion electrode with polynitrobenzene amine as sensitive membrane and preparation method thereof |
| CN106066354B (en) * | 2016-05-24 | 2018-10-02 | 浙江大学 | Using polynitrobenzene amine as nitrate ion electrode of sensitive membrane and preparation method thereof |
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