阅读说明：本技术 一种β-环糊精修饰的石墨电极、制备方法及应用 (A kind of graphite electrode of beta-cyclodextrin modified, preparation method and application ) 是由 马明明 梁娟丽 刘佳 于 2019-08-30 设计创作，主要内容包括：本发明β-环糊精修饰的石墨电极,包括一端缠绕有铜丝的石墨棒,另一端的端面具有石蜡层,石墨棒表面电聚合有β-环糊精修饰层。本发明该β-环糊精修饰的石墨电极的制备方法,将石墨电极置于含有β-环糊精的缓冲溶液中通电,即得β-环糊精修饰的石墨电极。本发明应用β-环糊精修饰的石墨电极检测邻甲氧基苯胺的方法,将β-环糊精修饰的石墨电极按照三电极工作体系连接后置于待测溶液中检测峰电流,利用利用峰电流与邻甲氧基苯胺浓度之间的关系计算邻甲氧基苯胺。本发明采用电聚合法以β–CD修饰石墨电极,利用差分脉冲伏安法优化了制备条件。应用制备出的β-环糊精修饰的石墨电极对邻甲氧基苯胺进行检测,其处理简单、检测周期短。(The graphite electrode of beta-cyclodextrin modified of the present invention has the graphite rod of copper wire including one ends wound, and the end face of the other end has paraffin layer, and graphite rod surface electropolymerization has beta-cyclodextrin modified layer.Graphite electrode is placed in the buffer solution containing beta-cyclodextrin and is powered to get the graphite electrode of beta-cyclodextrin modified by the preparation method of the graphite electrode of the present invention beta-cyclodextrin modified.The method of the graphite electrode detection o-aminoanisole of present invention application beta-cyclodextrin modified, the graphite electrode of beta-cyclodextrin modified is placed in solution to be measured according to the connection of three electrode work systems and detects peak current, calculates o-aminoanisole using using the relationship between peak current and o-aminoanisole concentration.The present invention uses electropolymerization with β-CD Modified graphite electrode, optimizes preparation condition using differential pulse voltammetry.O-aminoanisole is detected using the graphite electrode for the beta-cyclodextrin modified prepared, processing is simple, detection cycle is short.)

1. a kind of graphite electrode of beta-cyclodextrin modified, which is characterized in that including graphite rod, the one ends wound of the graphite rod has The end face of copper wire, the other end has paraffin layer, and there is beta-cyclodextrin modified layer on the graphite rod surface by electropolymerization.

2. a kind of preparation method of the graphite electrode of beta-cyclodextrin modified as described in claim 1, which is characterized in that specifically press Implement according to following steps:

Step 1, graphite electrode is prepared；

Step 2, the graphite electrode is placed in the buffer solution containing beta-cyclodextrin, passes through electricity in the graphite electrode surface β-cyclodextrin polymer decorative layer to get beta-cyclodextrin modified graphite electrode.

3. preparation method as claimed in claim 2, which is characterized in that the step 1 specifically:

Step 1.1, graphite rod is provided, cleaned, dry it is rear spare；

Step 1.2, it will be put into paraffin molten liquid a period of time by the processed graphite rod of step 1.1, then take out and dry It is spare；

Step 1.3, it is wrapped in one end of the graphite rod after copper wire being polished and is fixed；

Step 1.4, it is cleaned after the graphite rod being carried out grinding and buffing, then seals the graphite rod not using paraffin The end face of one end of copper wire is wound to get the graphite electrode.

4. preparation method as claimed in claim 2, which is characterized in that the step 2 specifically:

Step 2.1, the graphite electrode is placed in buffer solution, contains beta-cyclodextrin in the buffer solution；

Step 2.2, the graphite electrode in buffer solution is powered, it is continuous in scanning potential range limiting after being enriched with several seconds Several circles of scan round, obtain the graphite electrode of the beta-cyclodextrin modified.

5. preparation method as claimed in claim 4, which is characterized in that the pH of the buffer solution is 5.2~7.4, described slow The beta-cyclodextrin concentration rushed in solution is 1.0 × 10^-4mol·L^-1~6.0 × 10^-3mol·L^-1；The buffer solution is mixing Acid-sodium hydroxide buffer solution, PBS buffer solution, disodium hydrogen phosphate-citric acid solution, potassium dihydrogen phosphate-sodium hydroxide Buffer solution or potassium dihydrogen phosphate-borax buffer solution.

6. preparation method as claimed in claim 4, which is characterized in that in the step 2.2, enrichment time is 60~160s, In -0.2~1.4V scanning potential range, with 10~50mVs^-1Fast continuous scan round 8~28 of sweeping enclose.

7. a kind of method of the graphite electrode detection o-aminoanisole using beta-cyclodextrin modified, which is characterized in that specific packet Include following steps:

Step 1, after by the graphite electrode of beta-cyclodextrin modified according to the connection of three electrode work systems, three electrodes are placed in be measured molten In liquid；

Step 2, the relation formula utilized between peak current and o-aminoanisole concentration is utilized:

I_p=(0.0674 ± 0.0026) c+9.550 × 10^-7±6.38×10^-9 (1)

Solution to be measured is detected,

Wherein, I_pIndicate peak point current, unit A；C indicates the concentration of o-aminoanisole, unit molL^-1。

8. the method for the graphite electrode detection o-aminoanisole of beta-cyclodextrin modified the use as claimed in claim 7, special Sign is that the three electrodes work system includes the CHI610D electrochemical workstation and computer of signal connection, described CHI610D electrochemical workstation is equipped with working electrode interface, reference electrode interface and auxiliary electrode interface totally 3 electrode interfaces, The working electrode interface, reference electrode interface and auxiliary electrode interface respectively with the graphite electrode of the beta-cyclodextrin modified, Saturated calomel electrode, platinum electrode are correspondingly connected with.

9. the method for the graphite electrode detection o-aminoanisole of beta-cyclodextrin modified the use as claimed in claim 7, special Sign is that the formula (1) in the step 2 obtains in accordance with the following steps:

Firstly, three electrodes of the three electrode work systems connected to be put into the buffer solution sample of the o-aminoanisole containing standard In solution；After being enriched with 60~160s under differential pulse method, linearly lied prostrate under conditions of scanning current potential and being -0.2~1.4V Peace scanning, records peak current I_p,

Wherein, the concentration of the buffer solution sample solution Plays o-aminoanisole is 9.0 × 10^-6~5.0 × 10^{- 5}mol·L^-1；

Then, by analyzing the peak current I measured_p, peak current I_pWith buffer solution sample solution Plays o-aminoanisole Meet formula (1) between concentration value.

10. the method for the graphite electrode detection o-aminoanisole of beta-cyclodextrin modified the use as claimed in claim 7, special Sign is, the specific detection process of the step 2 are as follows:

Step 2.1, three electrodes of three electrode work systems are put into solution to be measured, are powered on；

Step 2.2, under differential pulse method, be enriched with 60~160s after, scanning current potential be scanning current potential be -0.2~1.4V Under conditions of carry out linear voltammetric scan, record peak current I_p；

Step 2.3, by the peak current I of o-aminoanisole in the solution to be measured measured_pSubstitute into formula (1) in, can calculate to Survey the concentration of o-aminoanisole in solution.

Technical field

The invention belongs to analysis detection field of material technology, and in particular to a kind of graphite electrode of beta-cyclodextrin modified, also It is related to the preparation method of the graphite electrode, and the method using the graphite electrode detection o-aminoanisole prepared.

Background technique

O-aminoanisole is also known as 2- aminoanisole, can be used as the intermediate for producing dyestuff, medicine etc., have toxicity, Sensitization can cause the allergic reaction of respiratory system and skin.Currently, detection o-aminoanisole method have compounds GC-MS, Dispersive solid-phase extraction purification/Liquid Chromatography-Tandem Mass Spectrometry, zero stream potentiometry etc., but all there is instrument price in chromatographic mass spectrometry etc. Valuableness, complex pretreatment, detection cycle is long, and to the demanding disadvantage of operative skill.

Beta-cyclodextrin (β-CD) is a kind of cyclic polysaccharide, has hydrophilic exterior surfaces and hydrophobic interior cavities.Since its packet connects Function can security application in fields such as food, drug, chemical industry, pesticides.Electrode modification object material can also be done, the electricity made using it Pole can be used for detecting the concentration of o-aminoanisole.

Summary of the invention

The purpose of the present invention is to provide a kind of graphite electrode of beta-cyclodextrin modified, solves detection O-methoxy at present The problem that the existing processing of the instrument of aniline is complicated, detection cycle is long.

The object of the invention is also to provide a kind of preparation methods of the graphite electrode of above-mentioned beta-cyclodextrin modified.

The object of the invention is also to provide a kind of graphite electrodes using above-mentioned beta-cyclodextrin modified to detect O-methoxy The method of aniline.

The first technical solution of the present invention is: a kind of graphite electrode of beta-cyclodextrin modified, including graphite rod, The one ends wound of the graphite rod has copper wire, and the end face of the other end has paraffin layer, and the graphite rod surface has by electropolymerization Beta-cyclodextrin modified layer.

Second of technical solution of the present invention is: a kind of graphite electrode of beta-cyclodextrin modified as described above Preparation method is specifically implemented according to the following steps:

Step 1, graphite electrode is prepared；

Step 2, the graphite electrode is placed in the buffer solution containing beta-cyclodextrin, it is logical in the graphite electrode surface Electropolymerization beta-cyclodextrin modified layer is crossed to get the graphite electrode of beta-cyclodextrin modified.

Further, the step 1 specifically:

Step 1.1, graphite rod is provided, cleaned, dry it is rear spare；

Step 1.2, it will be put into paraffin molten liquid a period of time by the processed graphite rod of step 1.1, then take out It dries spare；

Step 1.3, it is wrapped in one end of the graphite rod after copper wire being polished and is fixed；

Step 1.4, it is cleaned after the graphite rod being carried out grinding and buffing, then seals the graphite using paraffin Stick does not wind the end face of one end of copper wire to get the graphite electrode.

Further, the step 2 specifically:

Step 2.1, the graphite electrode is placed in buffer solution, contains beta-cyclodextrin in the buffer solution；

Step 2.2, the graphite electrode in buffer solution is powered, after being enriched with several seconds, is being limited in scanning potential range Several circles of continuous scan round, obtain the graphite electrode of the beta-cyclodextrin modified.

Further, the pH of the buffer solution is 5.2~7.4, and the beta-cyclodextrin concentration in the buffer solution is 1.0×10^-4mol·L^-1~6.0 × 10^-3mol·L^-1；The buffer solution is mixed acid-sodium hydroxide buffer solution, PBS is slow Rush solution, disodium hydrogen phosphate-citric acid solution, potassium dihydrogen phosphate-sodium hydroxide buffer solution or potassium dihydrogen phosphate-borax Buffer solution.

Further, in the step 2.2, enrichment time is 60~160s, in -0.2~1.4V scanning potential range, With 10~50mVs^-1Fast continuous scan round 8~28 of sweeping enclose.

The third technical solution of the present invention is: a kind of adjacent first of graphite electrode detection using beta-cyclodextrin modified The method of oxygroup aniline, specifically comprises the following steps:

Step 1, by the graphite electrode of beta-cyclodextrin modified according to three electrode work systems connection after, by three electrodes be placed in It surveys in solution；

Step 2, the relation formula utilized between peak current and o-aminoanisole concentration is utilized:

I_p=(0.0674 ± 0.0026) c+9.550 × 10^-7±6.38×10^-9 (1)

Solution to be measured is detected,

Wherein, I_pIndicate peak point current, unit A；C indicates the concentration of o-aminoanisole, unit molL^-1。

Specifically, the three electrodes work system includes the CHI610D electrochemical workstation and computer of signal connection, institute Stating CHI610D electrochemical workstation, totally 3 electrodes connect equipped with working electrode interface, reference electrode interface and auxiliary electrode interface Mouthful, the working electrode interface, reference electrode interface and auxiliary electrode interface are electric with the graphite of the beta-cyclodextrin modified respectively Pole, saturated calomel electrode, platinum electrode are correspondingly connected with.

Further, the formula 1 in the step 2 obtains in accordance with the following steps:

Firstly, three electrodes of the three electrode work systems connected to be put into the buffer solution of the o-aminoanisole containing standard In sample solution；After being enriched with 60~160s under differential pulse method, line is carried out under conditions of scanning current potential and being -0.2~1.4V Property voltammetric scan, record peak current I_p,

Wherein, the concentration of the buffer solution sample solution Plays o-aminoanisole is 9.0 × 10^-6~5.0 × 10^-5mol·L^-1；

Then, by analyzing the peak current I measured_p, peak current I_pWith buffer solution sample solution Plays O-methoxy benzene Meet formula (1) between the concentration value of amine.

Further, the specific detection process of the step 2 are as follows:

Step 2.1, three electrodes of three electrode work systems are put into solution to be measured, are powered on；

Step 2.2, under differential pulse method, after being enriched with 60~160s, scanning current potential be scanning current potential be -0.2~ Linear voltammetric scan is carried out under conditions of 1.4V, records peak current I_p；

Step 2.3, by the peak current I of o-aminoanisole in the solution to be measured measured_pIt substitutes into formula (1), Ji Keji Calculate the concentration of o-aminoanisole in solution to be measured.

The beneficial effects of the present invention are: the present invention uses electropolymerization with β-CD Modified graphite electrode, differential pulse is utilized Voltammetry optimizes the various preparation conditions of the graphite electrode of β-CD modification, prepares beta-cyclodextrin modified in optimal conditions Graphite electrode.The voltammetric behaviors of o-aminoanisole are studied and carried out using the graphite electrode for the beta-cyclodextrin modified prepared Trace detection, compared to chromatographic mass spectrometry detection method, processing is simple, detection cycle is short.

Detailed description of the invention

Fig. 1 is the cyclic voltammetry curve figure for the graphite electrode that electropolymerization prepares beta-cyclodextrin modified in the method for the present invention；

Fig. 2 is tradition three electrode system schematic device used in the present invention；

Fig. 3 is the condition optimizing figure for the graphite electrode that electropolymerization in the present invention prepares beta-cyclodextrin modified；

Fig. 4 be beta-cyclodextrin modified in the present invention graphite electrode in various concentration o-aminoanisole concentration and peak electricity The graph of relation of stream；

Fig. 5 is the cyclic voltammetry curve figure of the graphite electrode detection o-aminoanisole of beta-cyclodextrin modified in the present invention；

Fig. 6 is the differential pulse voltammetry curve of three kinds of Different electrodes detection o-aminoanisoles in the present invention.

Specific embodiment

The following describes the present invention in detail with reference to the accompanying drawings and specific embodiments.

As shown in Fig. 2, the graphite electrode 1 of beta-cyclodextrin modified provided by the invention, including graphite rod 12, graphite rod 12 One ends wound has copper wire 13 and, the end face parafilm wrap formation paraffin layer 10 of graphite rod 12 other end fixed by AB glue 11, There is beta-cyclodextrin modified layer on 12 surface of graphite rod by electropolymerization.

The invention also discloses the preparation methods of the graphite electrode of above-mentioned beta-cyclodextrin modified (β-CD/PEC) a kind of, specifically It follows the steps below to implement:

Step 1, graphite electrode is prepared；Specifically:

Step 1.1, graphite rod is provided, cleaned, dry it is rear spare；

Step 1.1 is in order to by understanding the impurity on graphite rod.The present invention using the most common Pencil with 2B hardness core as For graphite rod, illustrate its cleaning process: the layer of wood that Pencil with 2B hardness removal is rolled in outside (is guaranteed that pencil wicking surface is not drawn Wound), it is cut into the segment of about 1.6cm, successively in nitric acid aqueous solution (nitric acid is 1:1 with water volume ratio) solution, dehydrated alcohol and secondary steaming Supersound washing 5min is distinguished in distilled water, is dried spare.

Step 1.2, it will be put into paraffin molten liquid a period of time by the processed graphite rod of step 1.1, make its surface Become more smooth, guarantee its conducting continuity, stability, then take out dry it is spare；

Step 1.3, it is wrapped in one end of graphite rod after copper wire being polished and is fixed；

Step 1.4, dehydrated alcohol and secondary distilled water supersound washing 5min are used after graphite rod being carried out grinding and buffing, is gone Except surface impurity, then using paraffin seal graphite rod do not wind copper wire one end end face to get graphite electrode.

Step 2, graphite electrode is placed in the buffer solution containing beta-cyclodextrin, passes through electropolymerization in graphite electrode surface Beta-cyclodextrin modified layer to get beta-cyclodextrin modified graphite electrode.It specifically includes:

Step 2.1, graphite electrode is placed in buffer solution, beta-cyclodextrin is contained in buffer solution；Wherein, buffer solution PH be 5.2~7.4, the beta-cyclodextrin concentration in buffer solution is 1.0 × 10^-4mol·L^-1~6.0 × 10^-3mol·L^-1；It is slow Rushing solution is mixed acid-sodium hydroxide buffer solution, PBS buffer solution, disodium hydrogen phosphate-citric acid solution, di(2-ethylhexyl)phosphate Hydrogen potassium-sodium hydroxide buffer solution or potassium dihydrogen phosphate-borax buffer solution.

Step 2.2, the graphite electrode in buffer solution is powered, after being enriched with 60~160s, in the scanning of -0.2~1.4V In potential range, with 10~50mVs^-1Fast continuous scan round 8~28 of sweeping enclose, obtain the graphite electricity of beta-cyclodextrin modified Pole.

Fig. 1 is the electropolymerization curve graph for preparing the graphite electrode of beta-cyclodextrin modified；As seen from Figure 1, beta-cyclodextrin There is not oxidation peak and reduction peak on the electropolymerization cyclic voltammetry curve of the graphite electrode of modification, illustrates in scan round process In, there is no generation redox reactions by β-CD itself, and with the increase of scanning circle number, cyclic voltammetry curve is essentially coincided, It tends towards stability.

Invention additionally discloses a kind of methods of graphite electrode detection o-aminoanisole using beta-cyclodextrin modified, specifically Include the following steps:

Step 1, by the graphite electrode of beta-cyclodextrin modified according to three electrode work systems connection after, by three electrodes be placed in It surveys in solution 4；Wherein, which includes the CHI610D electrochemical workstation 8 and computer 9 of signal connection, CHI610D electrochemical workstation 8 is equipped with working electrode interface 5, reference electrode interface 6 and auxiliary electrode interface 7, and totally 3 electrodes connect Mouthful, working electrode interface 5, reference electrode interface 6 and auxiliary electrode interface 7 respectively with the graphite electrode of beta-cyclodextrin modified 1, full It is correspondingly connected with calomel electrode 3, platinum electrode 2.

Step 2, the relation formula utilized between peak current and o-aminoanisole concentration is utilized:

I_p=(0.0674 ± 0.0026) c+9.550 × 10^-7±6.38×10^-9 (1)

Solution to be measured is detected,

In above formula, I_pIndicate peak point current, unit A；C indicates the concentration of o-aminoanisole, unit molL^-1。

Formula (1) obtains in accordance with the following steps:

Firstly, three electrodes of the three electrode work systems connected to be put into the buffer solution of the o-aminoanisole containing standard In sample solution；After being enriched with 60~160s under differential pulse method, line is carried out under conditions of scanning current potential and being -0.2~1.4V Property voltammetric scan, record peak current I_p,

Wherein, the concentration of buffer solution sample solution Plays o-aminoanisole is 9.0 × 10^-6~5.0 × 10^{- 5}mol·L^-1；

Then, by analyzing the peak current I measured_p, peak current I_pWith buffer solution sample solution Plays O-methoxy benzene Meet formula (1) between the concentration value of amine.

The specific detection process of step 2 are as follows:

Step 2.1, three electrodes of three electrode work systems are put into solution to be measured, are powered on；

Step 2.2, under differential pulse method, after being enriched with 60~160s, scanning current potential be scanning current potential be -0.2~ Linear voltammetric scan is carried out under conditions of 1.4V, records peak current I_p；

Step 2.3, by the peak current I of o-aminoanisole in the solution to be measured measured_pIt substitutes into formula (1), Ji Keji The concentration of o-aminoanisole in solution to be measured is calculated, and then o-aminoanisole can be calculated according to liquor capacity to be measured Content.

Using beta-cyclodextrin modified prepared by the present invention graphite electrode to the o-aminoanisole solution of various concentration into Row detection, is respectively 9.0 × 10 in o-aminoanisole concentration^-6、1.0×10^-5、2.0×10^-5、3.0×10^-5、4.0×10^-5、5.0×10^-5mol·L^-1When, obtain the curve in Fig. 4.From left to right successively indicate that o-aminoanisole concentration is in Fig. 4 9.0×10^-6、1.0×10^-5、2.0×10^-5、3.0×10^-5、4.0×10^-5、5.0×10^-5mol·L^-1.The standard of various concentration When the disodium hydrogen phosphate of o-aminoanisole-citric acid solution sample solution is tested, the opposite I measured_pNumerical value Between there are certain rules, with I_pFor ordinate, c is abscissa, can obtain concentration c and peak current I by mapping_pCorresponding close System as shown in figure 4, it can be seen from curve in figure I_pRelationship between c meets formula (1).

Using the three-electrode system device of Fig. 2, after being tested using method of the invention it is found that test side of the invention Method is limited to 3.38 × 10 for the detection of o-aminoanisole^-6mol·L^-1, it can be seen that the detection spirit of detection method Sensitivity is high.

The present invention also tests the o-aminoanisole rate of recovery, specifically:

The sample containing o-aminoanisole is collected, electrode of the invention is put into actual sample according to above-mentioned experimental method In solution (rose liquid distilled from honeysuckle flowers or lotus leaves), the peak current I of the graphite electrode of beta-cyclodextrin modified is measured_p, according to formula (1), calculate in sample The content of o-aminoanisole, the results are shown in Table 1.

The recovery of standard addition of o-aminoanisole in 1 rose liquid distilled from honeysuckle flowers or lotus leaves of table

From table 1 it follows that the graphite electrode for the beta-cyclodextrin modified prepared using method of the invention carries out neighbour When aminoanisole is tested, the rate of recovery meets the requirements.

The present invention has also carried out the selectivity verifying of the graphite electrode of beta-cyclodextrin modified, specifically:

Interfering substance listed by first row in table 2 is separately added into o-aminoanisole solution, then according to utilization Each step that detection method of the invention detects o-aminoanisole is tested, and records its peak current I_P, real It is as shown in table 2 below to test result.

The influence of 2 interfering substance of table

As shown in Table 2, the graphite electrode selectivity of beta-cyclodextrin modified is illustrated when relative standard deviation is no more than ± 5% It is good.

Cyclic voltammetric response of the present invention also to o-aminoanisole in the graphite electrode of beta-cyclodextrin modified detects:

β-CD/PEC is containing 5.0 × 10^-5mol·L^-1Disodium hydrogen phosphate-citric acid that o-aminoanisole pH is 6.40 is slow The cyclic voltammetric response in solution is rushed, as shown in Figure 5, o-aminoanisole is on the cyclic voltammetric response curve on β-CD/PEC There is not reduction peak in only oxidation peak, illustrates that reaction of the o-aminoanisole on β-CD/PEC is an irreversible oxygen Change reduction process.

Pulse Voltammetry response of the present invention also to o-aminoanisole in β-CD/PEC, β-CD-PEC and PEC is tested, It is specifically implemented according to the following steps:

Step 1, it prepares pencil-core electrode and is pre-processed,

Step 1.1, pencil-lead is cut into the segment of 1.6cm, successively in nitric acid aqueous solution (V_HNO3With V_H2ORatio be 1:1) it is molten Supersound washing 5min is distinguished in liquid, dehydrated alcohol and secondary distilled water, is dried spare；

Step 1.2, the electrode prepared by step 1.1 is put into 20min in paraffin molten liquid, and taking-up is dried spare；

Step 1.3, copper wire is cut into the segment for being about 7cm, wipes the paint of two end surfaces of copper wire about 1cm long off, polishes Pencil-lead one end handled by winding step 1.2 afterwards, and fixed with AB glue.

Step 1.4, electrode prepared by step 1.3 is polishing to effective length with fine sandpaper is about 1.2cm or so, is used Its cylindrical surface of paper polishing is weighed, with dehydrated alcohol and secondary distilled water supersound washing 5min, electrode surface impurity is removed, then uses Paraffin seals the cross section after polishing, dries spare.

Step 2, β-CD/PEC is prepared,

Step 2.1, by PEC, saturated calomel electrode and platinum electrode that step 1.4 prepares be placed in containing β-CD (6.0 × 10^-3mol·L^-1) disodium hydrogen phosphate-citric acid solution (pH 6.40) in, in the scanning potential range of 0.3-0.9V Under, with 0.1Vs^-1(required preparation time 126s) is enclosed in sweep speed scan round 20, is taken out, and rinses number with second distillation flowing water It is secondary, it dries spare.

Step 3, natural immersion β-CD modified electrode (β-CD-PEC) is prepared

Step 3.1, PEC step 1.4 prepared is put into β-CD (6.0 × 10^-3mol·L^-1) disodium hydrogen phosphate-lemon In lemon acid buffering solution (pH 6.40), identical preparation time (126s), natural immersion under laboratory environment is taken out, and use is secondary It distills flowing water to rinse for several times, dry spare.

The present invention has detected β-CD/PEC, β-CD-PEC and PEC containing 1.0 × 10^-5mol·L^-1O-aminoanisole pH For the differential pulse voltammetry response in 6.40 disodium hydrogen phosphate-citric acid solution.As shown in fig. 6, it is found that β-CD/PEC (the differential pulse voltammetry response peak current of curve a) is maximum, illustrates that the β-CD/PEC of electropolymerization preparation is more stable and to adjacent first The response sensitivity of oxygroup aniline is stronger；(curve b) peak current takes second place β-CD-PEC, illustrates that part β-CD enters in soaking process Effective ratio area to the surface PEC, electrode surface is small, just few subsequently into the O-methoxy benzene on β-CD-PEC, and volt-ampere is rung Induction signal is also weaker than the β-CD/PEC of electropolymerization formation；(peak current of curve c) is minimum, illustrates that β-CD enhances the sound of PEC by PEC Induction signal.The peak current and spike potential of three kinds of electrodes are as shown in table 3, by data it follows that β-CD/PEC is than the peak β-CD-PEC Electric current is about 1.2 times high, than nearly 2.3 times of PEC high.

The spike potential and peak current of 3 three kinds of electrode Different electrodes of table

In addition, the graphite electrode in order to illustrate beta-cyclodextrin modified is good to the analysis measurement stability of o-aminoanisole It is good, by the graphite electrode of same root beta-cyclodextrin modified 1.0 × 10^-5mol·L^-1The phosphoric acid that o-aminoanisole pH is 6.40 It being every other day measured in parallel once in disodium hydrogen-citric acid solution, the peak point current that METHOD FOR CONTINUOUS DETERMINATION is 10 times is as shown in table 4, The relative standard deviation of peak point current is 2.69%, illustrates analysis of the graphite electrode to o-aminoanisole of beta-cyclodextrin modified Measurement has good stability.

4 electrodes of table every other day measure 1 peak point current

The reproducibility of the graphite electrode of the beta-cyclodextrin modified prepared to illustrate the invention is fine.It is repaired with five beta-cyclodextrins The graphite electrode of decorations detects 1.0 × 10 respectively^-5mol·L^-1O-aminoanisole, the results are shown in Table 5, the opposite mark of peak current Quasi- deviation is 4.31%, illustrates the reproducibility that the graphite electrode of beta-cyclodextrin modified has had the detection of o-aminoanisole.

5 different batches of table, five electrode runs parallels measure the peak point current of 5 measurements