阅读说明：本技术 一种耐低温多元共聚尼龙树脂及其合成方法 (Low-temperature-resistant multi-component copolymerized nylon resin and synthetic method thereof ) 是由 邓凯桓 王文志 毛新华 于 2019-09-09 设计创作，主要内容包括：本发明涉及一种耐低温多元共聚尼龙及其合成方法。以己内酰胺与66盐、葵二胺葵二酸盐、葵二酸己二胺盐,612盐,等单体在250-280℃,0.3-1.5MPa条件下共聚反应8-10小时,得到相对粘度为2.8-3.2的共聚尼龙树脂。其组成为：己内酰胺：共聚单体比例为70-90：10-30.所得共聚尼龙树脂具有优异的耐低温性能,常温缺口冲击强度为90kj/m<Sup>2</Sup>缺口冲击不断,--40缺口冲击强度为35kj/m<Sup>2</Sup>,可用于普通尼龙树脂的增韧剂,软管,单丝,及弹性纤维等领域。(The invention relates to low-temperature-resistant multicomponent copolymerized nylon and a synthesis method thereof. The copolymerization reaction of caprolactam with 66 salt, sebacic diamine sebacic acid salt, sebacic acid adipic diamine salt, 612 salt and other monomers is carried out for 8-10 hours at the temperature of 250-280 ℃ and under the pressure of 0.3-1.5MPa, so as to obtain the copolymer nylon resin with the relative viscosity of 2.8-3.2. The composition is as follows: caprolactam: the proportion of the comonomer is 70-90:10-30, the obtained copolymer nylon resin has excellent low temperature resistance and normal temperature notch impact strength of 90kj/m 2 The notch impact is constant, and-40 notch impact strength is 35kj/m 2 It can be used in the fields of toughening agent of common nylon resin, hose, monofilament and elastic fiber, etc.)

1. A low temperature resistant multi-component copolymerized nylon resin and a synthetic method thereof are characterized by comprising the following steps: at least two or more than two comonomers are copolymerized by using caprolactam as a main body, and the composition ratio, namely the ratio of the caprolactam to the comonomers is 70-90: 10-30.

2. The low temperature resistant multicomponent copolymer nylon resin and the synthesis method thereof according to claim 1, characterized in that:

wherein the comonomers are: the proportion of the first comonomer is 10-20%, the proportion of the second comonomer is 5-15%, and the proportion of the third comonomer is 1-5%;

the comonomer comprises sebacic acid salt of sebacic acid, adipic acid salt of adipic acid, adipic acid salt of sebacic acid, hexamethylenediamine salt of adipic acid, hexamethylenediamine glutarate, hexamethylenediamine adipate and dodecylamine dodecanoate;

the first and third comonomers comprise sebacic acid salt of sebacic acid, adipic acid salt of sebacic acid, and dodecylamine dodecanoic acid salt;

the second comonomer comprises hexamethylenediamine glutarate, hexamethylenediamine adipate.

3. The low temperature resistant multicomponent copolymer nylon resin and the synthesis method thereof according to claim 2, characterized in that: the first comonomer and the third comonomer are 106 salt, 610 salt, 612 salt and 1212 salt; the second comonomer is a 56 salt; the proportion of the first comonomer is 15-20%, the proportion of the second comonomer is 8-12%, and the proportion of the third key monomer is 2-4%.

4. The low temperature resistant multicomponent copolymer nylon resin and the synthesis method thereof according to claim 3, characterized in that: the copolymerization process is a continuous polymerization process, and the industrialization of the multi-component copolymerized nylon resin is realized by using a PA6 continuous polymerization production line, and comprises the processes of comonomer salifying, copolymerization, extraction, drying and tackifying.

5. The low temperature resistant multipolymer nylon resin and the synthesis method thereof as claimed in claim 4, characterized in that: the salt forming process and the process of the comonomer are as follows: the method comprises three procedures of salt forming reaction of key monomers, crystallization of comonomer salt and separation of the comonomer, and the specific process comprises the following steps:

firstly, adding deionized water or ethanol into a salt forming kettle, controlling the molar ratio of dibasic acid to diamine to be 1.0-1.15, controlling the pH value to be 7.2-7.8, controlling the reaction temperature to be 60-90 ℃, and reacting for 2-4 hours;

cooling and crystallizing: after the step I is finished, reducing the temperature of the reaction kettle to 10-40 ℃, and crystallizing for 1-2 hours;

③ separating: and after crystallization is finished, opening a discharge valve of the reaction kettle, and allowing the crystallized salt solution to enter a separator to complete separation of crystals and water to obtain the comonomer salt.

6. The low temperature resistant multipolymer nylon resin and the synthesis method thereof as claimed in claim 5, characterized in that: the temperature of the comonomer salifying reaction is 70-80 ℃, the PH is 7.3-7.5, the reaction time is 2.5-3.5 hours, and the molar ratio of the dibasic acid to the diamine is 1.05-1.10; the crystallization temperature is 20-35 ℃, and the crystallization time is 1.2-1.8 hours.

7. The low temperature resistant multipolymer nylon resin and the synthesis method thereof as claimed in claim 4, characterized in that: the preparation process of comonomer salt solution includes the preparation and storage of key monomer salt solution, and includes the following steps:

preparation of aqueous solution of comonomer salt: sequentially adding deionized water or deionized water/ethanol mixed solution into a preparation kettle, wherein the ratio of water to ethanol is 1-4:1, and the concentration of the comonomer is 60-75%; the comonomer salt can be two or three salts, wherein the addition amount of the long carbon chain comonomer salt is 15-20%, the addition amount of the second comonomer is 8-12%, the addition amount of the third comonomer salt is 2-4%, the dissolving temperature is 60-120 ℃, the dissolving time is 1-4 hours, the mixture is sent into a storage tank for standby after being dissolved, the comonomer salt storage tank keeps the solution state of the comonomer salt through the circulation of a circulating pump, and meanwhile, the temperature is kept to 80-90 ℃.

8. The low temperature resistant multipolymer nylon resin and the synthesis method thereof as claimed in claim 7, characterized in that: the solution is water/ethanol mixed solution, and the ratio of water to ethanol is 3: 1, the concentration of comonomer salt is 65-70%; the dissolving temperature is 70-95 ℃, and the dissolving time is 2-3 hours; the temperature of the comonomer salt solution is 70-90 ℃ for storage and heat preservation.

9. The low temperature resistant multipolymer nylon resin and the synthesis method thereof as claimed in claim 4, characterized in that: comprising the metering and polymerization of caprolactam and comonomer salts:

the process of conveying, tape injection, cooling and grain cutting of the copolymer resin melt comprises the following process steps:

the comonomer salt solution and the caprolactam liquid are respectively mixed according to the ratio of 10-35: 65-90, or 10-35% of comonomer salt and 65-90% of caprolactam; continuously metering and conveying the mixture into the top of a polymerization pipe, wherein the polymerization reaction temperature of the polymerization pipe is 240 ℃ plus 260 ℃ before the top, and the polymerization reaction temperature of the middle part is as follows: 250 ℃ and 280 ℃, lower part: 240 ℃ and 260 ℃; the pressure of the polymerization pipe is 1-5 MPa; continuously conveying the copolymer into a melt die head from a bottom plate of a polymerization pipe through a melt pump to form a strip, cooling the strip to enter a granulator for granulation, wherein the cooling temperature is 20-30 ℃; the unextracted copolymer resin has a relative viscosity of 2.8 to 3.2.

10. The low temperature resistant multipolymer nylon resin and the synthesis method thereof as claimed in claim 9, characterized in that: the polymerization process is divided into three stages; the first stage is hydrolysis and polycondensation of caprolactam to form low molecular polycondensate; the second stage is a chain growth reaction stage, and the copolymerization reaction at the stage forms a copolymer with a certain molecular weight; the third stage is post-polymerization, and the molecular weight of the copolymer at the stage is further increased to obtain the copolymer with the relative viscosity of more than 2.8; the feeding amount of the comonomer salt is 20-35%, the feeding amount of the caprolactam is 65-80%, the pre-polymerization temperature is 240 ℃ and 250 ℃, and the middle part: 250-: 240 ℃ and 250 ℃; the pressure of the polymerization pipe is 2-4 MPa; the cooling temperature of the injection belt is 20-25 ℃.

11. The low temperature resistant multipolymer nylon resin and the synthesis method thereof as claimed in claim 4, characterized in that: the extraction process of the copolymer resin comprises the following steps: comprises water bath ratio, extraction temperature and time; the water bath ratio is 2.5-4.0; the extraction temperature is 85-105 ℃, and the extraction retention time is 6-9 hours; the process is that after being cooled and cut into particles, the copolymer is continuously sent to the top of an extraction tower, resin particles are from top to bottom, and water is from bottom to top; the copolymer nylon resin contains about 7 percent of unreacted caprolactam and oligomers thereof, and is separated from the copolymer nylon resin through water extraction, so that the oligomer content in the copolymer resin is ensured to be less than 0.2 percent.

12. The low temperature resistant multipolymer nylon resin and the synthetic method thereof as claimed in claim 11, wherein: the extraction temperature of the copolymer resin is 90-95 ℃, the water bath ratio is 3.5-4.0, and the extraction time is 7-8 hours.

13. The low temperature resistant multipolymer nylon resin and the synthesis method thereof as claimed in claim 4, characterized in that: drying and tackifying process; continuous drying and tackifying are carried out, a two-stage drying tackifying process is adopted, the first stage adopts high-temperature nitrogen drying, and the second stage adopts a low-temperature nitrogen and vacuum drying tackifying process;

the process comprises the following steps: feeding the copolymer resin separated from the bottom of the extraction tower into the top of a drying tower through high-temperature nitrogen, and enabling the resin slices to pass through two drying towers connected in series from top to bottom; the temperature of the top of the first drying tower is 80-110 ℃, the temperature of the middle part is 80-100 ℃, the temperature of the lower part is 70-90 ℃, and the retention time is 10-15 hours; temperature of the second drying tower: top 70-90 ℃, middle: 60-80 ℃, bottom: the retention time is 10-15 hours at 20-40 ℃, and the relative viscosity of the dried and tackified copolymer resin is 3.2-3.6.

14. The low temperature resistant multipolymer nylon resin and the synthetic method thereof as claimed in claim 13, wherein: the temperature of the top of the first drying tower is 80-100 ℃, the temperature of the middle part is 80-90 ℃, the temperature of the lower part is 70-80 ℃, and the retention time is 10-12 hours; the temperature of the second drying tower is 70-80 ℃ at the top part, and the temperature of the middle part: 60-70 ℃, bottom: the retention time is 10 to 12 hours at the temperature of between 30 and 40 ℃, and the relative viscosity of the dried and tackified copolymer resin is 3.2 to 3.6.

Technical Field

The invention relates to a copolymerized nylon resin, in particular to a low-temperature-resistant multicomponent copolymerized nylon resin and a synthetic method thereof.

Background

The nylon resin is the kind with the largest yield, the largest variety and the widest application in five engineering plastics. The nylon resin is divided into aromatic high-temperature resistant resin such as PA6T, PA9T, PA10T, PA46, PPA, PPTA and the like, long-carbon-chain low-temperature resistant resin such as PA11, PA12, PA612, PA1212 and the like, and aliphatic general-purpose resin such as PA6, PA66 and PA1010. the high-temperature resistant nylon resin is widely used for electronic appliances and automobile parts; general-purpose resins are widely used for automobile mechanical structural parts; the low-temperature resistant resin has excellent flexibility and low-temperature impact resistance, and is widely used for automobile soft and low-temperature impact resistant automobile rail transit equipment parts; however, the long carbon chain nylon resin has a complicated preparation technology of synthetic monomers and high cost, which leads to an over-high price of the resin, and thus, the application of the long carbon chain nylon resin is limited to a certain extent. Many researches on substitute products of long carbon chain nylon resin have been made, but industrialization has not been achieved due to technical immaturity.

Disclosure of Invention

The invention mainly solves the defects in the prior art, and aims to solve the problem that polycondensation is carried out on caprolactam and various dibasic acid diamine salts, namely, the caprolactam is used as a main monomer, long-carbon-chain dibasic acid and long-carbon-chain diamine are used as a second comonomer, and dibasic acid and diamine salts with different carbon chains are used as a third comonomer or a fourth comonomer; the prepared copolymerized nylon resin has low melting point, excellent low-temperature impact resistance and mechanical property close to that of long-carbon-chain nylon, and can replace low-temperature-resistant multi-copolymerized nylon resin in part of application fields of long-carbon-chain nylon and a synthetic method thereof.

The technical problem of the invention is mainly solved by the following technical scheme:

a low temperature resistant poly copolymer nylon resin and its synthesis method, using caprolactam as main body, at least two or more than two comonomers are copolymerized, its composition ratio, i.e. the ratio of caprolactam and comonomer is 70-90: 10-30;

wherein, the proportion of the first comonomer is 10-20%, the proportion of the second comonomer is 5-15%, and the proportion of the third comonomer is 1-5%;

the key monomers include sebacic acid salt, adipic acid diamine salt, sebacic acid diamine salt, adipic acid diamine sebacic acid salt, adipic acid diamine glutaric acid salt, 56 salt, adipic acid diamine salt, lauric acid amine salt and 1212 salt.

The first and third comonomers comprise sebacic acid salt, adipic acid diamine salt (106 salt), adipic acid sebacic acid diamine salt (610 salt), hexamethylenediamine sebacic acid salt (612 salt), sebacic acid diamine salt (126 salt) and dodecylamine dodecanoic acid salt (1212 salt); the second comonomer comprises hexamethylenediamine glutarate (56 salt), hexamethylenediamine adipate (66 salt).

Preferably, the first and third comonomers are 106, 610, 612, 1212 salts and the second comonomer is 56 salt; the proportion of the first comonomer is 15-20%, the proportion of the second comonomer is 8-12%, and the proportion of the third key monomer is 2-4%.

The copolymerization process is a continuous polymerization process. Comprises the processes of comonomer salifying, copolymerization, extraction, drying and tackifying.

The synthesis process of the multicomponent copolymerized nylon of the present invention may be intermittent polymerization or continuous copolymerization. The present invention adopts continuous copolymerization process, and features that on the basis of PA6 synthesizing line, there are added copolymer salt synthesizing, copolymer salt solution compounding kettle, storage tank, metering pump and other equipment, and the present invention can utilize PA6 continuous polymerization line to produce multicomponent copolymer nylon.

The invention relates to a comonomer salifying process and a process thereof: the method comprises three procedures of salt forming reaction of key comonomer, comonomer salt crystallization and comonomer separation, and the specific process comprises the following steps:

firstly, adding deionized water or ethanol into a salt forming kettle, controlling the molar ratio of dibasic acid to diamine to be 1.0-1.15, controlling the pH value to be 7.2-7.8, controlling the reaction temperature to be 60-90 ℃, and reacting for 2-4 hours.

Cooling and crystallizing: after the step I is finished, the temperature of the reaction kettle is reduced to 10-40 ℃, the crystallization time is 1-2 hours,

③ separating: and after crystallization is finished, opening a discharge valve of the reaction kettle, and enabling the crystallized salt solution to enter a separator to finish separation of crystals and water. To obtain the comonomer salt.

The comonomer salifying process is basically the same, the salifying temperature of the long carbon chain monomer is slightly higher than the salifying temperature of 66 salts, other processes are basically the same, the process of the comonomer salifying process is more important, and when the reaction temperature is lower, the reaction speed is slower, and longer time is needed; when the reaction temperature is too high, water or ethanol may be gasified to drive diamine to be gasified, so that the molar ratio of dibasic acid to diamine in the reaction system is disordered, the pH value of the reaction system is reduced, and the salt forming reaction speed is reduced; the crystallization temperature has a great influence on the crystallization speed and the crystallization integrity of the comonomer salt, the crystallization temperature is too high, the crystallization speed is slow, crystal particles are fine and are not beneficial to the filtration and separation of the monomer salt, and when the crystallization temperature is too low, the crystal particles are coarse and uneven.

The temperature of the comonomer salifying reaction is 70-80 ℃, the PH is 7.3-7.5, the reaction time is 2.5-3.5 hours, and the molar ratio of the dibasic acid to the diamine is 1.05-1.10; the crystallization temperature is 20-35 ℃, and the crystallization time is 1.2-1.8 hours.

The preparation process of the comonomer salt solution comprises the steps of preparing and storing the key monomer salt solution. The process comprises the following steps:

preparation of aqueous solution of comonomer salt: sequentially adding deionized water or deionized water/ethanol mixed solution into a preparation kettle, wherein the ratio of water to ethanol is 1-4:1, and the concentration of the comonomer is 60-75%; the comonomer salt can be two or three salts, wherein the addition amount of the long carbon chain comonomer salt is 15-20%, the addition amount of the second comonomer is 8-12%, the addition amount of the third comonomer salt is 2-4%, the dissolving temperature is 60-120 ℃, the dissolving time is 1-4 hours, the mixture is sent into a storage tank for standby after being dissolved, the comonomer salt storage tank keeps the solution state of the comonomer salt through the circulation of a circulating pump, and meanwhile, the temperature is kept to 80-90 ℃.

In the preparation of the comonomer salt solution, it is effective to use a certain amount of ethanol in a proper amount in combination with water in order to provide the solubility of the monomers. However, the amount of ethanol added cannot be too large, and on the one hand, the gas pressure in the polymerization tube may be too high after the critical monomer is added into the polymerization tube due to the high volatility of ethanol. Meanwhile, the recycling of ethanol brings about certain dissolution treatment cost.

The solution is water/ethanol mixed solution, and the ratio of water to ethanol is 3: 1, the concentration of comonomer salt is 65-70%; the dissolving temperature is 70-95 ℃, and the dissolving time is 2-3 hours; the temperature of the comonomer salt solution is 70-90 ℃ for storage and heat preservation.

The synthesis process of the poly-copolymerized nylon comprises five working procedures of metering caprolactam and comonomer salt, polymerization, cooling, granulating, extracting and drying. Therein, the polymerization process is divided into three stages. The first stage is caprolactam hydrolysis and polycondensation to form copolymer low molecular polycondensate, and the second stage is continuous growth reaction stage, in which the copolymerization reaction forms copolymer with certain molecular weight; the third stage is post-polymerization, in which the molecular weight of the copolymer is further increased to obtain a copolymer having a relative viscosity of 2.8 or more. The process comprises the following steps:

the comonomer salt solution and the caprolactam liquid are respectively mixed according to the ratio of 10-35: 65-90, or 10-35% comonomer salt, 65-90% caprolactam. Continuously metering the polymerization reaction mixture into the top of a polymerization pipe, wherein the polymerization reaction temperature of the polymerization pipe is 240 ℃ plus 260 ℃ before the top, and the polymerization reaction temperature of the middle part is as follows: 250 ℃ and 280 ℃, lower part: 240 ℃ and 260 ℃; the pressure of the polymerization pipe is 1-5 MPa; the copolymer is continuously sent into a melt die head from a bottom plate of a polymerization pipe through a melt pump to form a strip, the strip is cooled and enters a granulator to be granulated, and the cooling temperature is 20-30 ℃. The unextracted copolymer resin has a relative viscosity of 2.8 to 3.2.

The comonomer is added to the top of the polymerization tube and then the caprolactolysis and the condensation reaction are carried out, the two reactions are carried out simultaneously, according to the research, when the reaction temperature is increased in the initial stage, the reaction speed is favorably increased, but when the reaction temperature is too high, the gas-phase caprolactam and the diamine are increased simultaneously, the water in the reaction system is easy to gasify, and the reaction speed is further reduced; when the reaction temperature is too low, the reaction speed is slow and the copolymerization time is long. Moreover, when designing the reaction temperature, the condensation reaction speed between aminocaproic acid, the condensation reaction between aminocaproic acid and comonomer, and the condensation reaction speed between comonomer should be considered, and the temperature suitable for the simultaneous execution of the three reactions must be selected to ensure the uniform distribution of the macromolecular chain groups of the copolymer resin, so as to obtain a completely random copolymer resin. Thereby improving the flexibility of the copolymer resin and enhancing the low-temperature impact resistance of the copolymer resin; the middle stage of polymerization is mainly to promote the growth of molecular weight, and the reaction temperature is properly raised to be beneficial to the growth of molecular weight; in the later period of polymerization, the viscosity of the polymerization system is high, the molecular weight growth speed is slow, meanwhile, the hydrolysis reaction exists in the reaction system besides the molecular chain growth reaction, and the existence of a small amount of water molecules in the polymerization system can cause the hydrolysis reaction of the polymer, and the two reactions exist simultaneously. Therefore, the polymerization temperature can be suitably lowered at the latter stage of polymerization.

In addition, because the melting point of the copolymerized nylon resin is low, the cooling temperature of the injection strip needs to be as low as possible, and the strip is favorably cut into particles.

Preferably, the comonomer salt feed is 20-35%, the caprolactam feed is 65-80%, the pre-polymerization temperature is 240 ℃ and 250 ℃, the middle part: 250-: 240 ℃ and 250 ℃; the pressure of the polymerization pipe is 2-4 MPa; the cooling temperature of the injection belt is 20-25 ℃.

The extraction process of the copolymer resin comprises the following steps: including water bath ratio, extraction temperature and time. The water bath ratio is 2.5-4.0; the extraction temperature is 85-105 ℃, and the extraction retention time is 6-9 hours.

The process is that after being cooled and cut into grains, the copolymer is continuously fed into the top of an extraction tower, resin particles are from top to bottom, and water is from bottom to top. The copolymer nylon resin contains about 7 percent of unreacted caprolactam and oligomers thereof, and the unreacted caprolactam and the oligomers thereof are separated from the copolymer nylon resin through water extraction, so that the content of the oligomers in the copolymer nylon resin is ensured to be less than 0.2 percent. Because of the low melting point of the copolymerized nylon, the temperature is basically between 85 and 105 ℃. In order to avoid agglomeration of the copolymer resin, the extraction temperature should be controlled to be low, and the extraction effect is ensured. The invention adopts high water bath ratio and low extraction temperature process.

Preferably, the extraction temperature of the copolymer resin is 90-95 ℃, the water bath ratio is 3.5-4.0, and the extraction time is 7-8 hours.

The invention relates to a drying and tackifying process. The invention comprises continuous drying and tackifying, which is different from the common PA6 drying process in that the invention adopts a two-stage drying tackifying process, wherein the first stage adopts high-temperature nitrogen gas drying, and the second stage adopts low-temperature nitrogen gas and vacuum drying tackifying process. The process comprises the following steps: the copolymer resin separated from the bottom of the extraction tower is sent to the top of the drying tower through high-temperature nitrogen, and the resin slices pass through the two drying towers which are connected in series from top to bottom. The temperature of the top of the first drying tower is 80-110 ℃, the temperature of the middle part is 80-100 ℃, the temperature of the lower part is 70-90 ℃, and the retention time is 10-15 hours; the temperature of the second drying tower is 70-90 ℃ at the top part, and the temperature of the middle part: 60-80 ℃, bottom: the retention time is 10-15 hours at 20-40 ℃, and the relative viscosity of the dried and tackified copolymer resin is 3.2-3.6.

Because the melting point of the copolymerized nylon is low, the resin slices are easy to agglomerate under the high-temperature drying condition, and in order to avoid high-technology agglomeration, a low-temperature vacuum drying process is required, and the drying time is properly prolonged.

Preferably, the temperature of the top of the first drying tower is 80-100 ℃, the temperature of the middle part is 80-90 ℃, the temperature of the lower part is 70-80 ℃, and the retention time is 10-12 hours; the temperature of the second drying tower is 70-80 ℃ at the top part, and the temperature of the middle part: 60-70 ℃, bottom: the retention time is 10 to 12 hours at the temperature of between 30 and 40 ℃, and the relative viscosity of the dried and tackified copolymer resin is 3.2 to 3.6.

The caprolactam used in the invention is provided by the pellin petrochemical industry, and is provided by the chemical industry of sebacic acid, sebacic diamine, dodecanedioic acid and 1212 salt mountain eastern cinnabar; adipic acid, hexamethylenediamine, and 66 salts are available from the nema group, and pentanediamine, sebacic acid, and diamine salts are commercially available.

The key nylon synthesized by the invention is that the performance detection is carried out according to the relevant standard:

intrinsic viscosity of resin: 3.2-3.6, test standard: FZ/T51004

Room temperature notch impact strength: ≧ 80kj/m²And (4) testing standard: ASTM D756-1993;

③ 40 ℃ notch impact strength: ≧ 20kj/m²And (4) testing standard: ASTM D756-1993

Bending strength: ≧ 35MPa, test standard: ASTM D790-2007;

the flexural modulus is less than or equal to 800MPa, and the test standard is as follows: ASTM D790-2007;

sixthly, tensile strength: ≧ 50MPa, test standard: ASTM D638-2014

Elongation percentage: test Standard ≧ 300: ASTM D790-2007;

therefore, the multi-component copolymerized nylon resin has excellent flexibility and low temperature resistance, and can replace part of application fields of long carbon chain nylon; the invention has simple synthesis process, can fully utilize PA6 continuous synthesis equipment to realize industrialization, and has wide development prospect.

Drawings

FIG. 1 is a schematic diagram of the copolymerization process in the present invention.

Detailed Description

The technical scheme of the invention is further specifically described by the following embodiments.