阅读说明：本技术 一种壳聚糖共聚物及其制备和应用 (Chitosan copolymer and preparation and application thereof ) 是由 高玉华 刘振法 王深琳 吴根修 张利辉 郑玉轩 于 2021-09-15 设计创作，主要内容包括：本发明公开了一种适用于市政废水的水处理剂壳聚糖共聚物,其制备方法如下：首先壳聚糖和苯甲醛反应,生成壳聚糖-苯甲醛席夫碱,用来保护壳聚糖分子上的氨基,然后和丙烯酸反应,生成O-羧乙基--苯甲醛壳聚糖席夫碱,再用盐酸酸化,脱去甲醛保护基后,再和聚琥珀酰亚胺反应,生成壳聚糖-丙烯酸-天冬氨酸共聚物,经提纯、过滤、干燥得棕黄色固体。本发明适用于市政废水中,具有优异的阻垢和缓蚀性能。(The invention discloses a water treatment agent chitosan copolymer suitable for municipal wastewater, which is prepared by the following steps: firstly, reacting chitosan with benzaldehyde to generate chitosan-benzaldehyde Schiff base which is used for protecting amino on chitosan molecules, then reacting with acrylic acid to generate O-carboxyethyl-benzaldehyde chitosan Schiff base, acidifying with hydrochloric acid, removing a formaldehyde protecting group, then reacting with polysuccinimide to generate chitosan-acrylic acid-aspartic acid copolymer, purifying, filtering and drying to obtain brown yellow solid. The invention is suitable for municipal wastewater, and has excellent scale inhibition and corrosion inhibition performance.)

1. A chitosan copolymer chitosan-acrylic acid-aspartic acid (CTS-AA-PSI) is characterized in that the structural formula of the chitosan-acrylic acid-aspartic acid (CTS-AA-PSI) is as follows:

wherein, m is 15-23, n is 6-10, p is 10-16, all of which are positive integers.

2. The chitosan copolymer chitosan-acrylic-aspartic acid (CTS-AA-PSI) of claim 1, wherein the chitosan copolymer has a number average molecular weight M of 2800 to 4500.

3. The method for preparing the chitosan copolymer of claim 1 or 2, comprising the steps of:

(1) synthesis of chitosan-benzaldehyde schiff base (CTS-BE):

chitosan and 100mL of distilled water were added to a three-necked flask in the presence of N₂Dropwise adding a benzaldehyde ethanol solution into the flask under the protection to form a light yellow precipitate; then washing with distilled water for three times, and drying to obtain chitosan-benzaldehyde Schiff base;

(2) synthesis of Chitosan-acrylic acid copolymer (O-CTS-AA):

dissolving chitosan-benzaldehyde and 0.1g of ammonium persulfate in 100mL of acetic acid solution, stirring the mixture at 80 ℃ for 0.5h under the protection of nitrogen, dropwise adding a certain amount of Acrylic Acid (AA) solution, and continuing to react for 6 h; precipitating the product with acetone (200mL), washing the precipitate with absolute ethanol and filtering for 3 times, drying at 60 ℃ for 1h to obtain O-carboxyethyl and-benzaldehyde chitosan Schiff base, adding 100mL of 10 vol% hydrochloric acid solution to acidify the O-carboxyethyl and-benzaldehyde chitosan Schiff base for 6h, then precipitating the acidified product with acetone, and washing the precipitate with ethanol to obtain chitosan-acrylic acid copolymer (O-CTS-AA);

(3) synthesis of Polysuccinimide (PSI):

polysuccinimide (PSI) is synthesized by thermal condensation of L-aspartic acid monomer in electrothermal constant temperature drying oven at 240 deg.c for 4 hr, and PSI is added into distilled water to form PSI suspension;

(4) synthesis of Chitosan-acrylic acid-aspartic acid copolymer (CTS-AA-PSI):

dissolving O-CTS-AA and NaOH in 20mL of deionized water, adjusting the pH value of the solution to 11-12, dropwise adding the mixed solution into the PSI suspension at 40 ℃, stirring for reacting for 6 hours, adjusting the pH value to 4-5 by using a hydrochloric acid solution after the reaction is finished, washing by using absolute ethyl alcohol and precipitating to obtain a brown yellow chitosan copolymer product (CTS-AA-PSI).

4. The method according to claim 3, wherein the concentration of the chitosan solution and the benzaldehyde ethanol solution in step (1) is 0.02M.

5. The production method according to claim 3, wherein the benzaldehyde ethanol solution is added dropwise in the step (1) and then stirred at 60 ℃ for 12 hours; the drying step was carried out in a vacuum oven at 60 ℃ for 24 hours.

6. The production method according to claim 3, wherein the concentration of the chitosan-benzaldehyde in the step (2) is 0.01M, and the concentration of the acetic acid solution is 1 vol%; the molar ratio of the chitosan-benzaldehyde to the acrylic acid is 1: 3-1: 6, and more preferably 1: 5.

7. The method according to claim 3, wherein the concentration of O-CTS-AA in the step (4) is 0.01M.

8. The preparation method according to claim 3, wherein in the step (4), the molar ratio of O-CTS-AA to polysuccinimide is 1: 2-5, and more preferably 1: 4.

9. The preparation method according to claim 3, wherein in the step (4), the molar ratio of chitosan, acrylic acid and polysuccinimide is 1:5:2 to 1:5:5, and more preferably is 1:5: 4.

10. The chitosan copolymer chitosan-acrylic acid-aspartic acid (CTS-AA-PSI) as claimed in claim 1 or 2 is applied to the treatment of municipal wastewater as a water treatment agent, wherein the amount of the water treatment agent is 10-20 mg/L.

Technical Field

The invention belongs to the technical field of energy conservation and environmental protection, and particularly relates to preparation and application of a chitosan copolymer as a water treatment agent.

Background

The shortage of water resources is one of the most important global problems, and the consumption of cooling water accounts for about 70 percent of the total amount of industrial water, so that the industrial cooling water is recycled, the water consumption can be greatly reduced, and the sewage discharge amount can be reduced. However, since the circulating cooling water system is operated at a high multiple for a long time, scaling, corrosion, bacterial and algal growth and other problems are easily caused, and difficulty is caused in operation management of the circulating cooling water, the circulating cooling water needs to be treated. Adding water treatment agents to the recirculating cooling water system is the most direct and effective way to prevent fouling and corrosion of the system. At present, the economic and efficient scale and corrosion inhibitors generally contain sulfur, phosphorus or complex aromatic ring structures, which are harmful to the environment. Therefore, the development of a biodegradable and environment-friendly scale and corrosion inhibitor with high scale and corrosion inhibition performance is urgently needed. In past studies it was found that the use of biodegradable materials as inhibitors could effectively alleviate environmental problems, such materials including tannins, starch, polyaspartic acid, polyepoxysuccinic acid and Chitosan (CTS). However, these biodegradable materials have a common problem in that their scale and corrosion inhibition properties are not ideal. Because chitosan can be combined with polysaccharide, hydroxyl, amino and amide, and has strong ion chelating ability, the scale can be inhibited; meanwhile, the linear structure and the amino hydroxyl group of the metal surface adsorbing material have an adsorbing effect on the metal surface, and are beneficial to adsorbing to the metal surface. Therefore, it is a potential scale and corrosion inhibitor. However, chitosan is insoluble in water, which limits its application. Fortunately, chitosan molecules have a reactive side chain amino group on the second carbon and a hydroxyl group on the sixth carbon, and these reactive centers can be chemically modified to increase their solubility. Therefore, the development of the environment-friendly chitosan derivative as the scale and corrosion inhibitor has wide application prospect.

Chitosan is a partial N-deacetylated derivative of chitin, commonly found in the shells of insects and crustaceans, and in the cell walls of some fungi, and is the second largest biopolymer that is second only to cellulose in nature. The chitosan has good biocompatibility, biodegradability, hydrophilicity, nontoxicity and non-antigenicityAnd biological adhesion and cell affinity. The chitosan and the derivatives thereof are widely applied to the aspect of sewage treatment, and can be used as an adsorbent, a flocculating agent, a bactericide and the like to remove heavy metal ions, organic matters, inorganic matters, TOC, COD, turbidity, chromaticity and the like. However, the research of the chitosan derivative as the scale and corrosion inhibitor is still in the initial stage, and related literature reports at home and abroad are less. Static scale inhibition experiment method for investigating CO of carboxymethyl chitosan in certain concentration₃ ^2-In the presence of Ca²⁺The scale inhibition performance of the catalyst is discussed, and the scale inhibition rate, the dosage of the scale inhibitor, the solution temperature and Ca are discussed²⁺The relationship between concentration and solution pH. The results show that carboxymethyl chitosan is Ca²⁺Has obvious scale inhibition performance, and is a novel water treatment agent with development prospect.

Disclosure of Invention

The invention provides a chitosan copolymer which can be used as an environment-friendly water treatment agent and a preparation method and application thereof, aiming at the problems of scaling and corrosion in an industrial circulating cooling water system.

In order to achieve the purpose, the invention adopts the following technical scheme:

a chitosan copolymer chitosan-acrylic acid-aspartic acid (CTS-AA-PSI) has a structural formula as follows:

wherein, m is 15-23, n is 6-10, p is 10-16, all of which are positive integers.

Further, the number average molecular weight M of the chitosan copolymer is 2800-4500.

As another object of the present invention, the present invention also discloses a method for preparing the above chitosan copolymer, comprising the steps of:

(1) synthesis of chitosan-benzaldehyde schiff base (CTS-BE):

chitosan and 100mL of distilled water were added to a three-necked flask in the presence of N₂Dropwise adding benzaldehyde ethanol solution into the flask under the protectionA pale yellow precipitate formed; then washing with distilled water for three times, and drying to obtain chitosan-benzaldehyde Schiff base;

(2) synthesis of Chitosan-acrylic acid copolymer (O-CTS-AA):

dissolving chitosan-benzaldehyde and 0.1g of ammonium persulfate in 100mL of acetic acid solution, stirring the mixture at 80 ℃ for 0.5h under the protection of nitrogen, dropwise adding a certain amount of Acrylic Acid (AA) solution, and continuing to react for 6 h; the product was precipitated with acetone (200mL), the precipitate was washed with absolute ethanol and filtered 3 times, and dried at 60 ℃ for 1h to give O-carboxyethyl and-benzaldehyde chitosan Schiff base. 100mL of 10 vol% hydrochloric acid solution was added to acidify the O-carboxyethyl and benzaldehyde chitosan Schiff base for 6h, and then the acidified product was precipitated with acetone and the precipitate was washed with ethanol to give chitosan-acrylic acid copolymer (O-CTS-AA).

(3) Synthesis of Polysuccinimide (PSI):

polysuccinimide (PSI) was synthesized by thermal condensation of L-aspartic acid monomer at 240 ℃ for 4 hours in an electrothermal thermostated drying oven, and PSI was added to distilled water to form a suspension of PSI for use.

(4) Synthesis of Chitosan-acrylic acid-aspartic acid copolymer (CTS-AA-PSI):

dissolving O-CTS-AA and NaOH in 20mL of deionized water, adjusting the pH value of the solution to 11-12, dropwise adding the mixed solution into the PSI suspension at 40 ℃, stirring for reacting for 6 hours, adjusting the pH value to 4-5 by using a hydrochloric acid solution after the reaction is finished, washing by using absolute ethyl alcohol and precipitating to obtain a brown yellow chitosan copolymer product (CTS-AA-PSI).

Preferably, in the step (1), the concentration of the chitosan solution and the benzaldehyde ethanol solution is 0.02M.

Preferably, the benzaldehyde ethanol solution is added dropwise in the step (1) and stirred at 60 ℃ for 12 h.

Preferably, step (1) is dried in a vacuum oven at 60 ℃ for 24 hours.

Preferably, the concentration of chitosan-benzaldehyde in step (2) is 0.01M and the concentration of acetic acid solution is vol 1%.

Preferably, the molar ratio of chitosan to acrylic acid in step (2) is 1:3 to 1:6, more preferably 1: 5.

Preferably, the concentration of O-CTS-AA in step (4) is 0.01M.

Preferably, in the step (4), the molar ratio of the O-CTS-AA to the polysuccinimide is 1: 2-5, and more preferably 1: 4.

Preferably, in the step (4), the molar ratio of the chitosan, the acrylic acid and the polysuccinimide is 1:5: 2-1: 5:5, and more preferably is 1:5: 4.

As another purpose of the invention, the invention also discloses application of the chitosan copolymer as a water treatment agent in treating municipal wastewater, wherein the dosage of the water treatment agent is 10-20 mg/L.

Compared with the prior art, the invention has the following beneficial effects:

the invention creatively provides a novel chitosan copolymer chitosan-acrylic acid-aspartic acid for water treatment, which is characterized in that chitosan reacts with benzaldehyde to generate chitosan-benzaldehyde Schiff base which is used for protecting amino on a chitosan molecule, then the chitosan copolymer chitosan-acrylic acid-aspartic acid reacts with acrylic acid to generate O-carboxyethyl-benzaldehyde chitosan Schiff base, the O-carboxyethyl-benzaldehyde chitosan Schiff base is acidified by hydrochloric acid, the formaldehyde protective group is removed, and then the O-benzaldehyde chitosan Schiff base reacts with polysuccinimide to generate a chitosan-acrylic acid-aspartic acid copolymer, and brown yellow solid is obtained after purification, filtration and drying. The chitosan-acrylic acid-aspartic acid copolymer as the water treatment agent synthesized by the invention is applied to municipal wastewater, and is concentrated by 2 times, and when the dosage is 15mg/L, the scale inhibition rate reaches 100%; meanwhile, the corrosion inhibitor has certain corrosion inhibition performance on A3 carbon steel, and the corrosion inhibition rate is 65.2%.

Drawings

FIG. 1 is an infrared spectrum of chitosan and chitosan-acrylic acid-aspartic acid copolymer of the present invention.

Detailed Description

The present invention is described in detail below with reference to the following embodiments and the attached drawings, it should be understood that the embodiments are only for illustrating the present invention and are not to be construed as limiting the present invention, and any modifications, equivalents and the like based on the present invention are within the scope of the present invention.

The invention provides a preparation method of chitosan-acrylic acid-aspartic acid, which comprises the following specific steps:

(1) synthesis of chitosan-benzaldehyde schiff base (CTS-BE):

in a three-necked flask, CTS (0.02M) and 100mL of distilled water were added under N₂An ethanol solution of benzaldehyde (0.02M) was added dropwise to the flask under protection, and stirred at 60 ℃ for 12 hours. The formed pale yellow precipitate was washed three times with distilled water and dried in a vacuum oven at 60 ℃ for 24 hours to obtain chitosan-benzaldehyde schiff base, the reaction equation is as follows:

(2) synthesis of Chitosan-acrylic acid copolymer (O-CTS-AA):

chitosan-benzaldehyde (0.01M) and 0.1g ammonium persulfate were dissolved in 100mL of acetic acid solution (1%). Stirring the mixture at 80 ℃ for 0.5h under the protection of nitrogen, then dropwise adding a certain amount of Acrylic Acid (AA) solution, wherein the molar ratio of chitosan to acrylic acid is 1: 3-1: 6, and continuously reacting for 6 h. The product was precipitated with acetone (200mL), the precipitate was washed with absolute ethanol and filtered 3 times, and dried at 60 ℃ for 1h to give O-carboxyethyl and-benzaldehyde chitosan Schiff base. 100mL of 10% hydrochloric acid solution (vol%) was added to acidify O-carboxyethyl and-benzaldehyde chitosan Schiff base for 6h, and then the acidified product was precipitated with acetone and the precipitate was washed with ethanol to give chitosan-acrylic acid copolymer (O-CTS-AA) according to the following reaction equation:

(3) synthesis of Polysuccinimide (PSI):

polysuccinimide (PSI) was synthesized by the thermal condensation of L-aspartic acid monomer at 240 ℃ for 4 hours in an electrothermal thermostatted drying oven. PSI was added to distilled water to form a PSI suspension for use, the reaction equation is as follows:

(4) synthesis of Chitosan-acrylic acid-aspartic acid copolymer (CTS-AA-PSI):

O-CTS-AA (0.01M) and NaOH were dissolved in 20mL deionized water and the solution pH was adjusted to 11-12. Dropwise adding the mixed solution into the PSI suspension at 40 ℃, and stirring for reaction for 6 hours, wherein the molar ratio of chitosan to acrylic acid to polysuccinimide is 1:5: 2-1: 5: 5. After the reaction is finished, the pH value is adjusted to 4-5 by hydrochloric acid solution, and the pH value is washed by absolute ethyl alcohol and precipitated to obtain a brown yellow chitosan copolymer product (CTS-AA-PSI), wherein the reaction equation is as follows:

wherein, m is 15-23, n is 6-10, p is 10-16, all of which are positive integers.

The process route design idea of the invention is as follows: the chitosan molecular structure has three reactive sites, namely C₂Amino in position, C₃、C₆The hydroxyl on the position is helpful to improving the scale inhibition performance due to the existence of the carboxyl, so as to introduce more carboxyl into the molecular structure of the chitosan to improve the scale inhibition performance, although the acrylic acid and the polyaspartic acid are relatively common green scale inhibitors, the scale inhibition effect is not ideal, and the chitosan, the acrylic acid and the polyaspartic acid are copolymerized to play a role in synergy. Chitosan is difficult to dissolve in water, and is easy to dissolve in 1% acetic acid solution, and polyaspartic acid usually exists in the form of polyaspartic acid sodium salt, so that direct mixing and compounding of the three are not feasible. Acrylic acid and polyaspartic acid are respectively introduced by utilizing two reactive sites on the molecular structure of chitosan, and the intermediate product Polysuccinimide (PSI) of polyaspartic acid is easy to carry out ammonolysis reaction under the alkaline condition, so that polyaspartic acid is introducedWhen in amino acid molecule, PSI is used as a reaction raw material, and chitosan can only react with acrylic acid first and then is grafted with polyaspartic acid. In the process of grafting acrylic acid, since acrylic acid is easily grafted to the amino at the 2-position and the hydroxyl at the 6-position, in order to ensure that the acrylic acid is completely grafted to the hydroxyl at the 6-position, the amino at the 2-position is firstly protected by a protecting group, then the protecting group is removed, and the reaction is carried out with PSI, and finally the chitosan copolymer-chitosan-acrylic acid-aspartic acid copolymer is generated.

As shown in FIG. 1, the infrared spectra of chitosan are respectively at 2879-3362, 1595, 1378, 1067 and 889cm^-1There are six distinct characteristic absorption peaks. Wherein, the position is 2879-3362cm^-1The wide vibration expansion region is-OH and-H₂A functional group. Located at 1595cm^-1The absorption peak at (A) is an absorption peak of the amide group. The deformed absorption peaks and the beta-D-structure peaks of methyl and methylene are respectively positioned at 1378 and 899cm^-1To (3). Is positioned at 1067cm^-1The absorption peaks are C-O and C-O-C tensile vibration absorption peaks. In the infrared spectrum of chitosan-acrylic acid-aspartic acid copolymer, -OH and-H₂The stretching vibration peak of the vibration sensor moves to 2981-3335cm^-1Where C ═ O has a stretching vibration absorption peak at 1713cm^-1Where C is an extension vibration peak shifted to 1647 cm^-1Here, successful grafting of AA and PSI into CTS resulted in an absorption peak at 1595-1534cm for the amide group^-1The beta-D-structure peak is 899cm^-1Moved to 897cm^-1To (3). In summary, the IR spectrum demonstrated the successful synthesis of chitosan-acrylic acid-aspartic acid copolymer (CTS-AA-PSI).

The present invention will be described in further detail with reference to examples, but the present invention is not limited to these examples.

Example 1

A preparation method of a chitosan copolymer water treatment agent comprises the following steps:

3.2g of chitosan is weighed, 100mL of distilled water is weighed into a three-neck flask, 2.1g of benzaldehyde-ethanol solution is dropwise added into the flask under the protection of nitrogen, and the mixture is stirred for 12 hours at the temperature of 60 ℃. The formed light yellow precipitate is washed with distilled water for three times and dried in a vacuum drying oven at 60 ℃ for 24h to obtain the chitosan-benzaldehyde Schiff base. 2.66g of chitosan-benzaldehyde and 0.1g of ammonium persulfate were dissolved in 100mL of a 1% acetic acid solution. The mixture was stirred at 80 ℃ for 0.5h under nitrogen, then 2.16g of acrylic acid solution was added dropwise and the reaction was continued for 6 h. Precipitating the product with 200mL of acetone, washing the precipitate with absolute ethanol, filtering for 3 times, and drying at 60 ℃ for 1h to obtain the O-carboxyethyl-benzaldehyde chitosan Schiff base. Acidifying O-carboxyethyl-benzaldehyde chitosan Schiff base with 100mL of 10% hydrochloric acid solution for 6h, then precipitating the acidified product with acetone, and washing the precipitate with ethanol to obtain chitosan-acrylic acid copolymer (O-CTS-AA). Polysuccinimide (PSI) was synthesized by thermal condensation of L-aspartic acid monomer at 240 ℃ for 4 hours in an electrothermal thermostated drying oven, and 1.94g of PSI was added to distilled water to form a suspension of PSI for use. 2.32g O-CTS-AA and NaOH were dissolved in 20mL deionized water and the solution pH was adjusted to 11-12. Dropwise adding the mixed solution into the PSI suspension at 40 ℃, and stirring to react for 6 hours, wherein the molar ratio of the chitosan to the acrylic acid to the polysuccinimide is 1:3: 2. After the reaction is finished, the pH value is adjusted to 4-5 by hydrochloric acid solution, and the mixture is washed by absolute ethyl alcohol and precipitated to obtain a brown yellow chitosan-acrylic acid-aspartic acid copolymer product (CTS-AA-PSI). The scale inhibitor is applied to municipal wastewater, the experiment temperature is 80 ℃, the concentration is 2 times, the medicine adding amount is 20mg/L, the scale inhibition rate is 86.6 percent, and the corrosion inhibition rate on A3 carbon steel is 49.8 percent.

Example 2

A preparation method of a chitosan copolymer water treatment agent comprises the following steps:

3.2g of chitosan is weighed, 100mL of distilled water is weighed into a three-neck flask, 2.1g of benzaldehyde-ethanol solution is dropwise added into the flask under the protection of nitrogen, and the mixture is stirred for 12 hours at the temperature of 60 ℃. The formed light yellow precipitate is washed with distilled water for three times and dried in a vacuum drying oven at 60 ℃ for 24h to obtain the chitosan-benzaldehyde Schiff base. 2.66g of chitosan-benzaldehyde and 0.1g of ammonium persulfate were dissolved in 100mL of a 1% acetic acid solution. The mixture was stirred at 80 ℃ for 0.5h under nitrogen, then 2.16g of acrylic acid solution was added dropwise and the reaction was continued for 6 h. Precipitating the product with 200mL of acetone, washing the precipitate with absolute ethanol, filtering for 3 times, and drying at 60 ℃ for 1h to obtain the O-carboxyethyl-benzaldehyde chitosan Schiff base. Acidifying O-carboxyethyl-benzaldehyde chitosan Schiff base with 100mL of 10% hydrochloric acid solution for 6h, then precipitating the acidified product with acetone, and washing the precipitate with ethanol to obtain chitosan-acrylic acid copolymer (O-CTS-AA). Polysuccinimide (PSI) was synthesized by thermal condensation of L-aspartic acid monomer at 240 ℃ for 4 hours in an electrothermal thermostated drying oven, and 3.88g of PSI was added to distilled water to form a suspension of PSI for use. 2.32g O-CTS-AA and NaOH were dissolved in 20mL deionized water and the solution pH was adjusted to 11-12. Dropwise adding the mixed solution into the PSI suspension at 40 ℃, and stirring to react for 6 hours, wherein the molar ratio of the chitosan to the acrylic acid to the polysuccinimide is 1:3: 4. After the reaction is finished, the pH value is adjusted to 4-5 by hydrochloric acid solution, and the mixture is washed by absolute ethyl alcohol and precipitated to obtain a brown yellow chitosan-acrylic acid-aspartic acid copolymer product (CTS-AA-PSI). The scale inhibitor is applied to municipal wastewater, the experiment temperature is 80 ℃, the concentration is 2 times, the medicine adding amount is 10mg/L, the scale inhibition rate is 85.8 percent, and the corrosion inhibition rate on A3 carbon steel is 52.6 percent.

Example 3

A preparation method of a chitosan copolymer water treatment agent comprises the following steps:

3.2g of chitosan is weighed, 100mL of distilled water is weighed into a three-neck flask, 2.1g of benzaldehyde-ethanol solution is dropwise added into the flask under the protection of nitrogen, and the mixture is stirred for 12 hours at the temperature of 60 ℃. The formed light yellow precipitate is washed with distilled water for three times and dried in a vacuum drying oven at 60 ℃ for 24h to obtain the chitosan-benzaldehyde Schiff base. 2.66g of chitosan-benzaldehyde and 0.1g of ammonium persulfate were dissolved in 100mL of a 1% acetic acid solution. The mixture was stirred at 80 ℃ for 0.5h under nitrogen, then 2.88g of acrylic acid solution was added dropwise and the reaction was continued for 6 h. Precipitating the product with 200mL of acetone, washing the precipitate with absolute ethanol, filtering for 3 times, and drying at 60 ℃ for 1h to obtain the O-carboxyethyl-benzaldehyde chitosan Schiff base. Acidifying O-carboxyethyl-benzaldehyde chitosan Schiff base with 100mL of 10% hydrochloric acid solution for 6h, then precipitating the acidified product with acetone, and washing the precipitate with ethanol to obtain chitosan-acrylic acid copolymer (O-CTS-AA). Polysuccinimide (PSI) was synthesized by thermal condensation of L-aspartic acid monomer at 240 ℃ for 4 hours in an electrothermal thermostated drying oven, and 1.94g of PSI was added to distilled water to form a suspension of PSI for use. 2.32g O-CTS-AA and NaOH were dissolved in 20mL deionized water and the solution pH was adjusted to 11-12. Dropwise adding the mixed solution into the PSI suspension at 40 ℃, and stirring to react for 6 hours, wherein the molar ratio of the chitosan to the acrylic acid to the polysuccinimide is 1:4: 2. After the reaction is finished, the pH value is adjusted to 4-5 by hydrochloric acid solution, and the mixture is washed by absolute ethyl alcohol and precipitated to obtain a brown yellow chitosan-acrylic acid-aspartic acid copolymer product (CTS-AA-PSI). The scale inhibitor is applied to municipal wastewater, the experiment temperature is 80 ℃, the concentration is 2 times, the medicine adding amount is 20mg/L, the scale inhibition rate is 88.6 percent, and the corrosion inhibition rate on A3 carbon steel is 57.9 percent.

Example 4

A preparation method of a chitosan copolymer water treatment agent comprises the following steps:

3.2g of chitosan is weighed, 100mL of distilled water is weighed into a three-neck flask, 2.1g of benzaldehyde-ethanol solution is dropwise added into the flask under the protection of nitrogen, and the mixture is stirred for 12 hours at the temperature of 60 ℃. The formed light yellow precipitate is washed with distilled water for three times and dried in a vacuum drying oven at 60 ℃ for 24h to obtain the chitosan-benzaldehyde Schiff base. 2.66g of chitosan-benzaldehyde and 0.1g of ammonium persulfate were dissolved in 100mL of a 1% acetic acid solution. The mixture was stirred at 80 ℃ for 0.5h under nitrogen, then 2.88g of acrylic acid solution was added dropwise and the reaction was continued for 6 h. Precipitating the product with 200mL of acetone, washing the precipitate with absolute ethanol, filtering for 3 times, and drying at 60 ℃ for 1h to obtain the O-carboxyethyl-benzaldehyde chitosan Schiff base. Acidifying O-carboxyethyl-benzaldehyde chitosan Schiff base with 100mL of 10% hydrochloric acid solution for 6h, then precipitating the acidified product with acetone, and washing the precipitate with ethanol to obtain chitosan-acrylic acid copolymer (O-CTS-AA). Polysuccinimide (PSI) was synthesized by the thermal condensation of L-aspartic acid monomer at 240 ℃ for 4 hours in an electrothermal thermostated drying oven, and 4.85g of PSI was added to distilled water to form a suspension of PSI for use. 2.32g O-CTS-AA and NaOH were dissolved in 20mL deionized water and the solution pH was adjusted to 11-12. Dropwise adding the mixed solution into the PSI suspension at 40 ℃, and stirring to react for 6 hours, wherein the molar ratio of the chitosan to the acrylic acid to the polysuccinimide is 1:4: 5. After the reaction is finished, the pH value is adjusted to 4-5 by hydrochloric acid solution, and the mixture is washed by absolute ethyl alcohol and precipitated to obtain a brown yellow chitosan-acrylic acid-aspartic acid copolymer product (CTS-AA-PSI). The scale inhibitor is applied to municipal wastewater, the experiment temperature is 80 ℃, the concentration is 2 times, the medicine adding amount is 10mg/L, the scale inhibition rate is 91.4 percent, and the corrosion inhibition rate on A3 carbon steel is 57.1 percent.

Example 5

A preparation method of a chitosan copolymer water treatment agent comprises the following steps:

3.2g of chitosan is weighed, 100mL of distilled water is weighed into a three-neck flask, 2.1g of benzaldehyde-ethanol solution is dropwise added into the flask under the protection of nitrogen, and the mixture is stirred for 12 hours at the temperature of 60 ℃. The formed light yellow precipitate is washed with distilled water for three times and dried in a vacuum drying oven at 60 ℃ for 24h to obtain the chitosan-benzaldehyde Schiff base. 2.66g of chitosan-benzaldehyde and 0.1g of ammonium persulfate were dissolved in 100mL of a 1% acetic acid solution. The mixture was stirred at 80 ℃ for 0.5h under nitrogen, then 3.6g of acrylic acid solution was added dropwise and the reaction was continued for 6 h. Precipitating the product with 200mL of acetone, washing the precipitate with absolute ethanol, filtering for 3 times, and drying at 60 ℃ for 1h to obtain the O-carboxyethyl-benzaldehyde chitosan Schiff base. Acidifying O-carboxyethyl-benzaldehyde chitosan Schiff base with 100mL of 10% hydrochloric acid solution for 6h, then precipitating the acidified product with acetone, and washing the precipitate with ethanol to obtain chitosan-acrylic acid copolymer (O-CTS-AA). Polysuccinimide (PSI) was synthesized by thermal condensation of L-aspartic acid monomer at 240 ℃ for 4 hours in an electrothermal thermostated drying oven, and 1.94g of PSI was added to distilled water to form a suspension of PSI for use. 2.32g O-CTS-AA and NaOH were dissolved in 20mL deionized water and the solution pH was adjusted to 11-12. Dropwise adding the mixed solution into the PSI suspension at 40 ℃, and stirring to react for 6 hours, wherein the molar ratio of the chitosan to the acrylic acid to the polysuccinimide is 1:5: 2. After the reaction is finished, the pH value is adjusted to 4-5 by hydrochloric acid solution, and the mixture is washed by absolute ethyl alcohol and precipitated to obtain a brown yellow chitosan-acrylic acid-aspartic acid copolymer product (CTS-AA-PSI). The scale inhibitor is applied to municipal wastewater, the experiment temperature is 80 ℃, the concentration is 2 times, the dosage is 15mg/L, the scale inhibition rate is 92.4 percent, and the corrosion inhibition rate on A3 carbon steel is 63.5 percent.

Example 6

A preparation method of a chitosan copolymer water treatment agent comprises the following steps:

3.2g of chitosan is weighed, 100mL of distilled water is weighed into a three-neck flask, 2.1g of benzaldehyde-ethanol solution is dropwise added into the flask under the protection of nitrogen, and the mixture is stirred for 12 hours at the temperature of 60 ℃. The formed light yellow precipitate is washed with distilled water for three times and dried in a vacuum drying oven at 60 ℃ for 24h to obtain the chitosan-benzaldehyde Schiff base. 2.66g of chitosan-benzaldehyde and 0.1g of ammonium persulfate were dissolved in 100mL of a 1% acetic acid solution. The mixture was stirred at 80 ℃ for 0.5h under nitrogen, then 3.6g of acrylic acid solution was added dropwise and the reaction was continued for 6 h. Precipitating the product with 200mL of acetone, washing the precipitate with absolute ethanol, filtering for 3 times, and drying at 60 ℃ for 1h to obtain the O-carboxyethyl-benzaldehyde chitosan Schiff base. Acidifying O-carboxyethyl-benzaldehyde chitosan Schiff base with 100mL of 10% hydrochloric acid solution for 6h, then precipitating the acidified product with acetone, and washing the precipitate with ethanol to obtain chitosan-acrylic acid copolymer (O-CTS-AA). Polysuccinimide (PSI) was synthesized by thermal condensation of L-aspartic acid monomer at 240 ℃ for 4 hours in an electrothermal thermostated drying oven, and 3.88g of PSI was added to distilled water to form a suspension of PSI for use. 2.32g O-CTS-AA and NaOH were dissolved in 20mL deionized water and the solution pH was adjusted to 11-12. Dropwise adding the mixed solution into the PSI suspension at 40 ℃, and stirring to react for 6 hours, wherein the molar ratio of the chitosan to the acrylic acid to the polysuccinimide is 1:5: 4. After the reaction is finished, the pH value is adjusted to 4-5 by hydrochloric acid solution, and the mixture is washed by absolute ethyl alcohol and precipitated to obtain a brown yellow chitosan-acrylic acid-aspartic acid copolymer product (CTS-AA-PSI). The scale inhibitor is applied to municipal wastewater, the experiment temperature is 80 ℃, the concentration is 2 times, the addition amount is 15mg/L, the scale inhibition rate is 100 percent, and the corrosion inhibition rate on A3 carbon steel is 65.2 percent.

Example 7

A preparation method of a chitosan copolymer water treatment agent comprises the following steps:

3.2g of chitosan is weighed, 100mL of distilled water is weighed into a three-neck flask, 2.1g of benzaldehyde-ethanol solution is dropwise added into the flask under the protection of nitrogen, and the mixture is stirred for 12 hours at the temperature of 60 ℃. The formed light yellow precipitate is washed with distilled water for three times and dried in a vacuum drying oven at 60 ℃ for 24h to obtain the chitosan-benzaldehyde Schiff base. 2.66g of chitosan-benzaldehyde and 0.1g of ammonium persulfate were dissolved in 100mL of a 1% acetic acid solution. The mixture was stirred at 80 ℃ for 0.5h under nitrogen, then 4.32g of acrylic acid solution was added dropwise and the reaction was continued for 6 h. Precipitating the product with 200mL of acetone, washing the precipitate with absolute ethanol, filtering for 3 times, and drying at 60 ℃ for 1h to obtain the O-carboxyethyl-benzaldehyde chitosan Schiff base. Acidifying O-carboxyethyl-benzaldehyde chitosan Schiff base with 100mL of 10% hydrochloric acid solution for 6h, then precipitating the acidified product with acetone, and washing the precipitate with ethanol to obtain chitosan-acrylic acid copolymer (O-CTS-AA). Polysuccinimide (PSI) was synthesized by the thermal condensation of L-aspartic acid monomer at 240 ℃ for 4 hours in an electrothermal thermostated drying oven, and 4.85g of PSI was added to distilled water to form a suspension of PSI for use. 2.32g O-CTS-AA and NaOH were dissolved in 20mL deionized water and the solution pH was adjusted to 11-12. Dropwise adding the mixed solution into the PSI suspension at 40 ℃, and stirring to react for 6 hours, wherein the molar ratio of the chitosan to the acrylic acid to the polysuccinimide is 1:6: 5. After the reaction is finished, the pH value is adjusted to 4-5 by hydrochloric acid solution, and the mixture is washed by absolute ethyl alcohol and precipitated to obtain a brown yellow chitosan-acrylic acid-aspartic acid copolymer product (CTS-AA-PSI). The scale inhibitor is applied to municipal wastewater, the experiment temperature is 80 ℃, the concentration is 2 times, the medicine adding amount is 10mg/L, the scale inhibition rate is 98.9 percent, and the corrosion inhibition rate on A3 carbon steel is 65.7 percent.

Comparative example

Compared with the prior art, when the dosage of the chitosan-maleic anhydride-itaconic acid copolymer scale inhibitor is increased from 20mg/L to 50 mg/L, the scale inhibition rate is increased rapidly and is increased from 35.3% to 86.6%, and when the dosage of the medicament is 60mg/L, the maximum scale inhibition rate is 91.6%. Polyaspartic acid/O-carboxymethyl chitosan is used as a scale inhibitor, and when the dosage of the polyaspartic acid/O-carboxymethyl chitosan is 100mg/L, the maximum scale inhibition rate on barium sulfate is 93.6%. The synthetic chitosan-acrylic acid copolymer (CTS-AA) is adopted as a scale inhibitor, the concentration of the synthetic chitosan-acrylic acid copolymer in municipal wastewater is 1.5 times, when the addition amount is 20mg/L, the scale inhibition performance is obviously superior to that of the monomer acrylic acid, the scale inhibition rate is respectively higher than 22% and higher than 18% compared with that of the commercially available polyacrylic acid and HEDP and reaches 76.7%, and when the addition amount is 30mg/L, the scale inhibition rate is 92.9%. The chitosan-acrylic acid-aspartic acid copolymer as the water treatment agent synthesized by the invention is applied to municipal wastewater, and is concentrated by 2 times, and when the dosage is 15mg/L, the scale inhibition rate reaches 100%; meanwhile, the corrosion inhibitor has certain corrosion inhibition performance on A3 carbon steel, and the corrosion inhibition rate is 65.2%.

The above description is only a preferred embodiment of the present invention, and all equivalent changes and modifications made in accordance with the claims of the present invention should be covered by the present invention.