854 results about "Caprolactam" patented technology

The invention discloses a biosynthesis system for high-yield 1, 6-hexamethylenediamine and application of the biosynthesis system, and belongs to the technical field of biology. According to the method, key genes which are excavated and optimized in a 1, 6-hexamethylenediamine biosynthetic pathway are co-expressed in a single cell module or a multi-cell module, and different enzyme elements expressed by the cell module are subjected to enzyme cascade reaction, so that 1, 6-hexamethylenediamine can be efficiently synthesized by taking caprolactam or 6-aminocaproic acid as a substrate; furthermore, after the carboxylic acid reductase MaCAR is mutated, the catalytic activity of the carboxylic acid reductase MaCAR can be remarkably improved, and the yield of the 1, 6-hexamethylenediamine is further improved; in addition, the biosynthesis system disclosed by the invention directly takes the cell module as a whole-cell catalyst, and an enzyme purification step is avoided, so that the biosynthesis system has the advantage of low cost.

The invention discloses a nylon elastomer preparation method, which comprises: S1, weighing preparation raw materials of a nylon elastomer according to a feeding ratio, and weighing the preparation raw materials by using a weighing device, the nylon elastomer is prepared from the following raw materials: tridecane diamine, tridecane dibasic acid, dodecanediamine, dodecanedioic acid, undecanediamine, undecanedioic acid, decamethylene diamine, sebacic acid, pentamethylene diamine, glutaric acid, hexamethylenediamine, adipic acid, caprolactam, and one or more of polyether amine and polyether alcohol; and S2, feeding the preparation raw materials weighed in the step S1. In the preparation process of the nylon elastomer, the nylon elastomer with different melting points, different crystallization temperatures, different strengths and different elongation at break is produced by adopting a multi-component copolymerization mode and adjusting the types and the molecular weights of polyether amine and polyether alcohol by adjusting the types and the proportions of binary acid and diamine, so that the nylon elastomer is suitable for different use environments; the utilization rate is improved.

The invention discloses functional caprolactam, an intrinsic flame-retardant nylon material as well as a preparation method and application thereof, and relates to the technical field of flame-retardant nylon materials. The preparation method comprises the following steps: preparing an alpha-amino-epsilon-caprolactam intermediate by taking lysine as an initial raw material through one-step efficient cyclization, then reacting with a reagent containing a flame-retardant group to obtain functional caprolactam, and finally introducing the flame-retardant group into a side chain of nylon 6 by utilizing ring-opening copolymerization of the functional caprolactam and caprolactam to prepare the intrinsic flame-retardant nylon material. The flame-retardant nylon material can effectively avoid the migration and loss of the flame retardant, improve the dispersity of the flame retardant and enhance the flame-retardant effect, can keep the main chain structure of the nylon 6 unchanged, reduces the influence on the inherent performance of the nylon 6, is expected to directly replace the existing nylon 6 material, and is applied to the fields of automobiles, textiles, electronics and electrics, buildings, packaging and the like. In addition, a renewable lysine resource is used for partially replacing a petroleum resource, so that the method has the advantages of resource conservation, environmental friendliness, simple process, low cost and the like.

The invention provides a hydrolysis method of a waste nylon 6 fishing net. The hydrolysis method comprises the following steps: step 1, screening the waste nylon 6 fishing net, cleaning, removing impurities, disinfecting and crushing; step 2, pretreating diatomite; step 3, adding pretreated diatomite, solid acid and deionized water into a reaction kettle, stirring at 50 DEG C for 5 hours, and removing moisture to obtain a solid acid catalyst; 4, adding the solid acid catalyst, the cleaned waste nylon 6 fishing net and deionized water into a reaction kettle, controlling the temperature and time for reaction, and filtering while hot to obtain a liquid-phase product; 5, neutralizing, decolorizing and extracting the liquid-phase product to obtain a caprolactam monomer; and 6, carrying out polymerization reaction on the obtained caprolactam monomer to generate regenerated polyamide for chinlon spinning. According to the method provided by the invention, the solid acid catalyst is easily separated from reactants, the catalytic efficiency is high, the corrosion to equipment can be reduced, and the method is more environment-friendly.

A high-strength PA6 composite material and a preparation method therefor, the PA6 composite material comprising, in parts by mass, 80-95 parts of caprolactam, 1-3 parts of benzoic acid and 10-30 parts of a modification additive. The benzoic acid is used for improving the tensile strength of the composite material, and the modification additive is used for enhancing the impact resistance of the composite material. Terephthalic acid and m-xylylenediamine undergo a reaction to generate m-xylylenediamine terephthalate, which is then subjected to a polycondensation reaction with caprolactam, so as to introduce same into the backbone of a PA6 molecule and modify the PA6 resin. The modified PA6 resin has remarkably improved tensile strength and impact resistance, so that the application range of the PA6 composite material can be greatly expanded.

The invention relates to the field of caprolactam production, and discloses a green and efficient production process and device. The process comprises the following steps: continuously oximating cyclohexanone and hydroxylamine in a microreactor under the catalysis of mesoporous silica solid acid; carrying out gas phase rearrangement on cyclohexanone-oxime in the presence of a ZSM-5 molecular sieve under the assistance of microwaves; coupling, rectifying and purifying the crude product through a four-stage molecular sieve membrane; and performing catalytic cracking on the by-product to obtain N2 / H2O and recycling. The device comprises a micro-reaction unit, a microwave-radial reactor, a membrane coupling rectifying tower group and a tail gas cracking unit. Zero emission of ammonium sulfate is achieved, the product purity is larger than or equal to 99.95%, and energy consumption is reduced by 45%.

The invention relates to the technical field of fabric waterproofing agents, in particular to a polyurethane modified organic silicon fluoride-free waterproofing agent and a preparation method thereof. The polyurethane modified organic silicon fluoride-free waterproof agent is prepared from the following raw materials in parts by mass: 5 to 15 parts of hexamethylene diisocyanate, 5 to 15 parts of butyl acrylate, 1 to 5 parts of methyl methacrylate, 40 to 60 parts of octamethylcyclotetrasiloxane, 10 to 30 parts of alpha, omega-dihydroxy polydimethylsiloxane and 5 to 10 parts of gamma-aminopropyl methyl diethoxy silane. The invention relates to a silane coupling agent, which is prepared from the following raw materials in parts by weight: 1 to 5 parts of glycidyl ether oxypropyl trimethoxy silane, 0.1 to 1 part of tetramethylammonium hydroxide, 0.1 to 1 part of triethylamine, 2 to 5 parts of tetraethoxysilane, 0.2 to 0.75 part of ammonia, 0.1 to 1 part of silane coupling agent KH-570, 0.01 to 0.1 part of dibutyltin dilaurate, 1 to 5 parts of epsilon-caprolactam, 1 to 2 parts of emulsifier and 0.1 to 1 part of initiator. The fabric treated by the method has good softness and excellent hydrophobic effect.

The invention relates to the technical field of organic synthesis, in particular to a synthesis method and application of functional caprolactam and functional nylon-6. The synthesis method comprises the following steps: in the presence of a catalyst and a solvent, enabling amino caprolactam and / or a derivative thereof to contact and react with benzaldehyde, so as to obtain functional caprolactam which is bis (benzyl) amino caprolactam, wherein the reaction conditions are as follows: the temperature is 150-350 DEG C; the hydrogen pressure is 0.1 to 10 MPa; the time is 5-15 hours. The synthesis method not only has the advantages of high reaction efficiency, high catalytic efficiency, adjustable target product selectivity and the like, but also simplifies process conditions, and realizes green large-scale production.

The invention discloses a hydroxylamine sulfate preparation method, which comprises: S1, carrying out analysis on caprolactam sulfate with water or a hydroxylamine sulfate aqueous solution to obtain a caprolactam sulfuric acid aqueous solution; extracting and separating the caprolactam sulfuric acid aqueous solution by using an extracting agent, conveying an extraction phase caprolactam organic solution to a caprolactam device for treatment, and entering a step S2 into a raffinate phase sulfuric acid aqueous solution or hydroxylamine sulfate and sulfuric acid aqueous solution; s2, adding ketoxime and a sulfuric acid aqueous solution or hydroxylamine sulfate and the sulfuric acid aqueous solution to generate a hydrolysis reaction to generate a hydroxylamine sulfate aqueous solution and ketone, and after ketone separation, sending the ketoxime to a ketoxime preparation device; s3, carrying out steam stripping separation on the hydroxylamine sulfate aqueous solution, sending unreacted ketoxime to the step S2 to participate in a hydrolysis reaction, and carrying out concentration crystallization, centrifugal filtration and drying dehydration on the hydroxylamine sulfate aqueous solution to obtain hydroxylamine sulfate; and S4, returning part of hydroxylamine sulfate raffinate subjected to centrifugal filtration to the step S1 for resolving caprolactam sulfate, and carrying out oximation reaction treatment on the residual hydroxylamine sulfate raffinate and ketone.

The invention discloses a carbon nano tube / caprolactam in-situ body synthesized nylon 6 composite material and a preparation method and application thereof, the material is prepared from a carbon nano tube, caprolactam and a catalyst through a body reaction processing technology, and the carbon nano tube is a single-wall or multi-wall carbon nano tube. The preparation method specifically comprises the following steps: firstly, uniformly mixing the raw materials according to a specific proportion, and then sequentially completing the conveying of low-viscosity raw materials, the self-initiation of polymerization reaction, macromolecular growth and the extrusion of high-viscosity products in a double-screw extruder, so that the caprolactam monomer is subjected to continuous chemical reaction and physical forming, and the caprolactam-based composite material is obtained. The conductive carbon nanotube modified nylon 6 composite material is obtained through one-step in-situ bulk polymerization. According to the invention, under the condition that only a trace amount of carbon nanotubes are added, the composite material can present excellent conductivity, the preparation method is simple and efficient, has a remarkable cost advantage and is easy for industrial production, and the morphological structure of the composite material can be flexibly regulated and controlled through molding equipment according to actual use requirements.

The present invention discloses an α-aminocaprolactam flame retardant containing a substituted P-C-N functional group, and a preparation method and application thereof. The flame retardant is prepared by a two-step reaction of three components, namely, α-aminocaprolactam, an aldehyde-containing compound, and an organophosphorus compound containing a P-H bond. First, the aldehyde-containing compound is reacted with the α-aminocaprolactam to obtain a Schiff base intermediate, which is then subjected to nucleophilic addition with the organophosphorus compound containing a P-H bond to obtain an α-aminocaprolactam substituted with a P-C-N functional group. The flame retardant of the present invention can introduce a variety of flame retardant elements including phosphorus, nitrogen, halogen, silicon and the like through the aldehyde-containing compound and the organophosphorus compound containing a P-H bond, thereby giving it good flame retardant properties; at the same time, the caprolactam group contained can be copolymerized with a variety of monomers or exchanged with a variety of polymers to prepare a variety of intrinsic flame-retardant polymers, and has broad application prospects.

The present disclosure relates to a method that includes hydrolyzing a polyamide by contacting the polyamide with a hydrolase. In some embodiments of the present disclosure, the polyamide may include nylon-6, nylon 6,6, or a combination thereof. In some embodiments of the present disclosure, the hydrolyzing may produce aminohexanoic acid, an oligomer of aminohexanoic acid, ε-caprolactam, or combinations thereof.

The invention discloses a thermal antistatic fabric based on polyamide fibers and a preparation method thereof, and relates to the technical field of textile fibers. When the thermal antistatic fabric based on the polyamide fiber is prepared, caprolactam, a flame retardant and hexamethylenediamine react to prepare pre-modified polyamide; the pre-modified chinlon and 3-chloro-1-propanethiol are subjected to a reaction, and modified chinlon is prepared; the preparation method comprises the following steps: sequentially reacting graphene oxide with mercaptopropyltrimethoxysilane and 2-(2H-benzotriazole-2-yl)-4-methyl-6-(2-propenyl) phenol, so as to obtain modified graphene oxide; the modified chinlon and the modified graphene oxide are mixed and then subjected to melt spinning, and modified chinlon fibers are obtained; and twisting the modified polyamide fiber, spinning, and post-processing to obtain the thermal antibacterial fabric based on the polyamide fiber. The warm-keeping antistatic fabric based on the polyamide fiber has good warm-keeping, antistatic, flame-retardant, anti-aging and mechanical properties.

The present disclosure provides siloxane derivatives of amino acids that have surface-active properties. The amino acid can be naturally-occurring or synthetic, or they may be obtained via a ring-opening reaction of a lactam, such as caprolactam. The amino acid may be functionalized with a siloxane group to form a compound that is surface-active and has surfactant characteristics. The compounds have low critical micelle concentrations (CMC) as well as the ability to lower the surface tension of a liquid.

Disclosed are a nylon-overmolded TPE composite material, a preparation method therefor and a use thereof. The nylon-overmolded TPE composite material of the present invention comprises: a hydrogenated styrene elastomer, mineral oil, polypropylene, polycaprolactam, a thermoplastic polyamide elastomer, maleic anhydride grafted polypropylene, a maleic anhydride grafted olefin copolymer elastomer, a maleic anhydride grafted hydrogenated styrene elastomer, a filler, and an additive. The nylon-overmolded TPE composite material combines polycaprolactam and a thermoplastic polyamide elastomer, along with other components; the use of the polycaprolactam enhances the strength of the composite material and improves the overmolding performance; moreover, the thermoplastic polyamide elastomer not only increases the elastomer content to improve the appearance of the composite material, but also can improve the overall compatibility of the polycaprolactam with the composite material; thus, a nylon-overmolded TPE composite material having high binding force, excellent mechanical properties and good appearance is obtained.

The present disclosure provides derivatives of amino acids that have surface-active properties. The amino acid can be naturally-occurring or synthetic, or they may be obtained via a ring-opening reaction of a lactam, such as caprolactam. The amino acid may be functionalized to form a compound that is surface-active and have advantageous surfactant characteristics. The compounds of the present disclosure have low critical micelle concentrations (CMC) as well as superior ability to lower the surface tension of a liquid.

The invention relates to a method for preparing polyamide 6 fine denier fibers through anionic polymerization. Caprolactam and a catalyst are added into a drying device A to remove system moisture and then placed in a storage tank A. Caprolactam is added into a drying device B to remove moisture and then placed in a storage tank B together with an initiator and a cyclic oligomer inhibitor. Caprolactam liquid in the storage tank A and the storage tank B is continuously injected into a screw extruder for anionic ring-opening polymerization reaction to prepare a polyamide 6 basic melt, the basic melt is further conveyed to a tandem devolatilization reaction system to remove monomers and part of cyclic oligomers to obtain a polyamide 6 final polymer, and finally, the polyamide 6 final polymer can be directly spun. The polyamide 6 fine denier fiber is obtained.

The invention provides a process method for chemically regenerating a PA6 product by using waste chinlon textiles, and belongs to the technical field of chinlon 6 waste recovery. According to the method, the waste chinlon textile is used as a raw material, refined caprolactam is obtained through depolymerization, flash evaporation, centrifugal separation and purification, and then the refined caprolactam is subjected to two-stage polymerization including front-stage pressurization and rear-stage decompression and a devolatilization process, so that the regenerated PA6 product is directly obtained. The PA6 melt prepared by the method is low in oligomer content, low in cyclic dimer content and low in caprolactam content, the regenerated PA6 product is excellent in performance, a new method is provided for resource reutilization of waste chinlon textiles, and the method has the advantages of being low in cost and easy to popularize.

The invention relates to the technical field of catalysts, in particular to a silicon-aluminum-based metal catalyst as well as a preparation method and application thereof, and a method for preparing dimethylaminocaprolactam. The modified aluminum oxide provided by the invention effectively reduces the density of B acid on the premise of ensuring certain density of L acid, and also has low wear index, high crushing strength, high specific surface area and low average pore size; meanwhile, the silicon-aluminum-based metal catalyst containing the modified aluminum oxide has relatively high catalytic activity, and has relatively high raw material conversion rate and target product selectivity when being particularly used for preparing dimethylaminocaprolactam.

The invention discloses a sulfonate grafted polyether-polyester-polyamide block copolymer and a synthesis method thereof, and belongs to the field of materials. The invention provides a block copolymer elastomer material taking polycaprolactam as a hard segment and polyether and polyester as soft segments, and specific sulfonic acid groups are introduced to meet specific applications. According to the invention, caprolactam, 6-aminocaproic acid, aliphatic dibasic acid, aliphatic diamine, polyether glycol, sulfonate grafted polyester polyol BY-3305 and the like are used as raw materials, and macromolecular sulfonate grafted polyester polyol BY-3305 is used as a sulfonate grafting agent, so that the reaction efficiency is higher than that of a small molecular monomer containing a sulfonic acid group, and fewer reaction byproducts are generated; the polymerization reaction can be smoothly carried out. The sulfonate grafted polyether-polyester-polyamide block copolymer elastomer is obtained through one-step melt polymerization, and has the advantages of being simple and convenient in synthesis method, low in production cost, high in strength, adjustable in performance and the like.

The invention discloses a full-bio-based multifunctional antibacterial nylon material as well as a preparation method and application thereof, relates to the technical field of high-molecular polymers, and solves the problems that the preparation process of a nylon material in the prior art depends on petroleum resources, the function is single and the application scene is limited. The method comprises the following steps: reacting an aminocaprolactam solution with corresponding aldehyde / carboxylic acid / halogenated alkane, and purifying to obtain a cyclic lysine derivative monomer M; the preparation method comprises the following steps: mixing and heating a cyclic lysine derivative monomer M, an initiator and a catalyst, reacting, and purifying to obtain a nylon material PM; and carrying out quaternization reaction on the nylon PM solution and alkyl halide, and purifying to obtain the full-bio-based multifunctional nylon material P. The preparation method completely abandons the use of petroleum-based raw materials, realizes the multifunctional synergistic effect of antibacterial property, biocompatibility, antibacterial biofilm property, thermosensitivity and the like, and can be applied to the fields of antibacterial materials, biomedical materials, antibacterial biofilms and thermosensitivity materials.

Disclosed is a process for hydrolytic depolymerization of a polyamide contained in a chemical feedstock F, wherein the process comprises: providing the chemical feedstock F; providing a liquid aqueous stream SW; preparing a mixture comprising the raw material F and the liquid aqueous stream SW and subjecting said mixture to polyamide 6 depolymerization conditions in a chemical reaction unit UR, thereby obtaining an aqueous stream SE exiting the UR, the stream SE comprising epsilon-caprolactam, wherein the mixture to be subjected to polyamide 6 depolymerization conditions comprises polyamide 6 and further comprises polyethylene terephthalate and polyamide 6.6 in a mass ratio rS = (mPA6.6 + mPET) / mPA6, wherein 0.01 < = rS < = 2.5.

The present disclosure provides siloxane derivatives of amino acids that have surface-active properties. The amino acid can be naturally-occurring or synthetic, or they may be obtained via a ring-opening reaction of a lactam, such as caprolactam. The amino acid may be functionalized with a siloxane group to form a compound that is surface-active and has surfactant characteristics. The compounds have low critical micelle concentrations (CMC) as well as the ability to lower the surface tension of a liquid.

A process for preparing a liquid high-purity ε-caprolactam stream ST, comprising preparing a liquid stream SC comprising ε-caprolactam, said preparing comprising depolymerizing a material M comprising polyamide 6, said liquid stream SC further comprising one or more oxidizable organic impurity compounds X, wherein the stream SC has an ε-caprolactam purity ΩGC(SC) of at least 99 %; providing a stream SO comprising at least one permanganate; preparing an oxidation reaction educt mixture MOE from the stream SC and the stream SO, and subjecting the mixture MOE to oxidation reaction conditions, obtaining an oxidation reaction product stream SP comprising ε-caprolactam, further comprising one or more oxidation products Y obtained from the oxidation of at least a part of the one or more compounds X, and optionally further comprising a part of the one or more organic compounds X; separating at least a part of the one or more oxidation products Y and optionally at least a part of organic compound X from the stream SP, obtaining the stream ST exhibiting an ε-caprolactam purity ΩGC(ST) of at least 99.5 % with ΩGC(ST) > ΩGC(SC), and an APHA value ΩGC(ST) of at most 10.

The present invention belongs to the technical field of petrochemical catalysis, and relates to a preparation method for improving the stability of a Cu-Beta zeolite catalyst for preparing caprolactam from caprolactone, and the use thereof. In the present invention, a cavity-modified dealuminated Beta zeolite is used as a carrier, and copper is loaded in pore channels of the zeolite carrier by means of an improved ammonia distillation method. The cavity modification refers to subjecting the dealuminated Beta zeolite carrier to a desiliconization technique controlled by the use of a weak organic base so as to enlarge silanol nests generated by dealumination of the dealuminated Beta zeolite carrier, thereby better accommodating and stabilizing the nano and sub-nano copper particles. The core of the improved ammonia distillation method involves impregnating a zeolite carrier with an equal volume of a copper-ammonia complex solution, such that the copper-ammonia complex mainly undergoes, during ammonia distillation, a reaction of depositing copper hydroxide in zeolite pore channels, thereby improving the sintering resistance. The Cu-Beta catalyst prepared using the method provided by the present invention exhibits high activity, selectivity and stability when applied to the reaction of caprolactam prepared from caprolactone via gas-solid phase hydroamination.

The invention relates to a method for preparing caprolactam, which is characterized in that: a # imgabs0 # acidic compound with temperature control phase transfer catalysis characteristics is adopted as a catalyst to catalyze cyclohexanone-oxime rearrangement reaction to prepare caprolactam, and the catalyst is recycled and reused; the conditions of the rearrangement reaction are as follows: the molar ratio of cyclohexanone-oxime to the catalyst is (10: 1)-(200: 1), the mass ratio of cyclohexanone-oxime to the organic solvent is (1: 1)-(1: 5), the reaction temperature is 40-150 DEG C, and the reaction time is 1-8 hours. The method has the characteristics that the # imgabs 1 # acidic compound with the temperature control phase transfer catalysis characteristic is used as a catalyst to catalyze cyclohexanone-oxime rearrangement reaction to prepare caprolactam, and has the characteristics of high-temperature homogeneous reaction-low-temperature two-phase separation; the reaction conditions are mild, the catalyst has good catalytic activity, the product yield is high, and the solvent and the catalyst are easy to separate and can be used.

The invention discloses a flexible hydrogel neural electrode and a preparation method and application thereof. The flexible hydrogel neural electrode comprises a flexible substrate layer, an electrode layer and a packaging layer which are sequentially arranged in a stacked mode, the flexible substrate layer and the packaging layer are each of a hydrogel fiber composite film structure formed by compounding a fiber film and hydrogel, and the fiber film is embedded in the hydrogel; the fiber film is a polycaprolactam fiber film, and the hydrogel is polyvinyl alcohol hydrogel; the electrode layer comprises a plurality of metal electrodes, and each metal electrode is provided with an electrode point and a bonding pad; the packaging layer is provided with a plurality of hole structures, and the holes are arranged corresponding to the electrode points and the bonding pads and enable the electrode points and the bonding pads to be exposed. The flexible hydrogel neural electrode provided by the invention has good biocompatibility, swelling resistance and process compatibility; meanwhile, the flexible hydrogel neural electrode can be stably applied to an implantable brain-computer interface and is used for realizing long-term stable acquisition and transmission of neural signals.

The invention discloses a catalyst for preparing 6-aminocapronitrile as well as a preparation method and application of the catalyst. The catalyst for preparing 6-aminocapronitrile comprises a carrier, an active component and a metal additive, the active component and the metal additive are loaded on the carrier; the carrier is a metal oxide and / or a non-metal oxide; the active component is an oxide of phosphorus; the metal additive is selected from at least one of a gallium compound, a niobium compound, an antimony compound and a ruthenium compound. The catalyst has excellent reaction activity and selectivity, the conversion rate of caprolactam can reach 99.5% or above, and the selectivity of 6-aminocapronitrile can reach 99.5% or above; the stability is good and the service life is long.

Provided is an ink composition for ultraviolet-curable inkjet printing comprising polymerization components, a resin component, and a photopolymerization initiator, wherein the polymerization components include (A) a polyfunctional amine-modified oligomer, (B) a nitrogen-containing monomer, (C) an aromatic ring-containing monomer, and (D) a polyfunctional monomer, wherein the resin component includes a hydroxyl group-containing resin, wherein (A) comprises an acrylated amine compound having two photopolymerizable functional groups and two amino groups in a molecule, wherein (B) comprises vinyl caprolactam, wherein (C) comprises benzyl acrylate and phenoxyethyl acrylate, wherein (D) comprises at least one of propoxylated neopentyl glycol diacrylate, dipropylene glycol diacrylate, or 1,6-hexanediol diacrylate, wherein a content of (A) is 0.1 to 13.0% by mass, wherein a content of (C) is 35.0 to 75.0% by mass, wherein a content of (D) is 2.0 to 16.0% by mass, and wherein the hydroxyl group-containing resin includes a ketone resin having a hydroxyl group.

The invention provides a polyamide hot melt adhesive containing dynamic reversible covalent bonds and a preparation method thereof, and belongs to the field of high polymer materials. Caprolactam and nylon 66 salt are used as raw materials, a furan ring and a carbon chain with a specific length are introduced, and the polyamide hot melt adhesive containing the dynamic reversible covalent bond is obtained through polymerization with maleimide and a derivative thereof. The melting point of the polymer can be regulated and controlled by regulating and controlling the carbon chain length of aliphatic diamine introduced into the xF salt, a furan ring in the xF salt is subjected to DA addition reaction with maleimide and a derivative thereof, dynamic reversible sites are provided, crosslinking between molecular chains is formed, a net system is formed, and the bonding strength of the material can be greatly improved. By adjusting the ratio of the xF salt to the maleimide and the derivative thereof, the reversible crosslinking behavior of the polymer can be adjusted, and finally the hot melt adhesive which has a lower melting point and excellent bonding strength and can be repeatedly used and recycled is obtained.