578 results about "Copolyester" patented technology

The invention relates to the technical field of multi-layer copolyester films, and discloses a high-temperature-resistant antistatic multi-layer copolyester film and a preparation method and application thereof, and the multi-layer copolyester film comprises an ABA three-layer structure obtained through melt co-extrusion; the layer A is prepared from the following raw materials in percentage by mass: 5 to 30 percent of anti-blocking agent master batch and the balance of modified copolyester; the raw material of the layer B is modified copolyester; the modified copolyester is prepared from a binary acid mixture, a dihydric alcohol mixture and a catalyst through an esterification reaction and a condensation polymerization reaction; the binary acid mixture comprises furandicarboxylic acid and 2, 2 '-bifuran-5, 5'-dicarboxylic acid, and the dihydric alcohol mixture comprises ethylene glycol, 2, 2, 4, 4-tetramethyl-1, 3-cyclobutanediol and 1, 4-cyclohexanedimethanol. According to the invention, the modified copolyester is used as a main raw material, and the film is endowed with good temperature resistance in a copolymerization modification manner, and has stable and lasting antistatic performance.

The invention discloses a full bio-based copolymer based on a citric acid bicyclic monomer, a preparation method and an application, and belongs to the technical field of material synthesis, citric acid-derived bicyclic OPD diol and OPBMC diester are synthesized through oxidation reduction and transesterification, and then 1, 4-butanediol is partially replaced with OPD or 2, 4-butanediol is partially replaced with OPBMC through melt phase polycondensation reaction. Two series of random copolyester PBxOyF copolymer and PBOmFn copolymer of the PBF are prepared by adding 2, 5-dimethyl furandicarboxylate into the PBF, and then adding the PBxOyF copolymer and the PBOmFn copolymer into the PBF. According to the full-bio-based copolymer based on the citric acid bicyclic monomer, the preparation method and the application, the citric acid bicyclic monomer obviously improves the glass transition temperature and shows good mechanical properties; therefore, the bicyclic monomer based on citric acid has huge potential in the aspect of synthesizing novel bio-based copolyester with expected thermodynamic properties, and is expected to further expand the application range of the 2.5 furandicarboxylic acid-based polyester.

The invention discloses a composite medical suture and a preparation method thereof, and belongs to the field of biomedicine. In order to solve the problems that an existing medical suture is poor in antibacterial effect and biological safety, the composite medical suture comprises a core layer, a degradation regulation and control layer, a slow release layer and an antibacterial layer which are sequentially arranged from inside to outside; the core layer is prepared from a blend fiber of poly (hydroxybutyrate-hydroxyvalerate) and polycaprolactone-co-polyglycolide; the degradation regulation and control layer comprises a mixture of at least two kinds of polyethylene glycol with different molecular weights; the slow release layer comprises quaternary ammonium salt loaded graphene oxide nanofibers; the antibacterial layer comprises titanium dioxide loaded with silver nanoparticles. Through the synergistic effect of the four layers, the comprehensive optimization of mechanical properties, degradation rate, drug sustained release and antibacterial function is realized; the purposes of improving the slow-release antibacterial performance, reducing damage to the human body, reducing inflammation and the like are achieved, and the antibacterial and degradation effects meet the recovery requirements.

The invention belongs to the technical field of copolymerization modification of degradable polyester, and relates to a depolymerization method and application of polybutylene terephthalate. During depolymerization, polybutylene terephthalate, dimethyl carbonate and dihydric alcohol are mixed and then subjected to a depolymerization reaction, and an intermediate ester is prepared; the dihydric alcohol is dihydric alcohol which does not form a ring with dimethyl carbonate in the depolymerization reaction process; the molar weight of the dimethyl carbonate is 10-30% of the molar weight of a repetitive unit of the polybutylene terephthalate; the sum of the molar weight of a 1, 4-butanediol unit in the polybutylene terephthalate and the molar weight of the added dihydric alcohol is a, the sum of the molar weight of a terephthalic acid unit in the polybutylene terephthalate and the molar weight of the added dimethyl carbonate is b, and the ratio of b to a is (1.2-1.5): 1; during application, the prepared intermediate ester is subjected to transesterification under the condition of negative pressure to obtain the copolyester. The depolymerization method is simple and easy to implement; the depolymerization product can be directly applied.

The invention provides a semi-crystalline transparent multicomponent copolyester and a preparation method thereof, and relates to the technical field of polyester synthesis. The preparation method of the semi-crystalline high-transparency multicomponent copolyester comprises the following steps: esterification reaction: mixing terephthalic acid, ethylene glycol, a branching agent, a modified monomer and a main catalyst, and carrying out esterification reaction to obtain an esterification product; and condensation polymerization: mixing the esterification product with a main catalyst, and carrying out condensation polymerization to obtain the semi-crystalline high-transparency multi-component copolyester, the mixture of the esterification reaction and / or the condensation polymerization reaction comprises a cocatalyst. According to the preparation method disclosed by the invention, polyester is subjected to copolymerization modification with relatively low content of alcohol and / or acid modified monomers to obtain the semi-crystalline multicomponent copolyester, and the semi-crystalline multicomponent copolyester is endowed with the advantages of high transparency, high hue, low cost, easiness in processing and the like.

The invention relates to an aliphatic copolyester elastomer and a preparation method thereof, and belongs to the field of high polymer materials. The elastomer is prepared through a series ring-opening copolymerization reaction of epoxide and cyclic anhydride, and the method comprises the following steps: under the action of a metal-free catalyst (a phosphazene ligand P1-tert-octyl / triethyl boron system) and an initiator (terephthalyl alcohol), carrying out a series ring-opening copolymerization reaction on epoxide and cyclic anhydride, the preparation method comprises the following steps: reacting epoxide (such as epoxypropane and allyl glycidyl ether) with aliphatic anhydride (such as glutaric anhydride) in a xylene solvent to generate a polyester prepolymer retaining an active end; adding a second group of epoxide (such as cyclohexene oxide) and anhydride (such as tetrahydrophthalic anhydride and norbornene dianhydride), continuously reacting to form a block copolymer, and then crosslinking. The material performance can be regulated by changing the monomer combination, the atom economy is high, and the raw materials can be produced on a large scale. The process is simple and environment-friendly, and a new choice is provided for application of the degradable elastomer in the fields of medical treatment, environmental protection and the like.

The present disclosure relates to a PET composite material and a preparation method therefor. The composite material comprises the following components in parts by mass: 50-100 parts of PET, 5-30 parts of an inorganic filler, and 5-30 parts of a PET copolyester. The PET copolyester is obtained by melting a waste pressure-sensitive adhesive product, adding an alcoholysis agent and a catalyst, and then performing polycondensation, wherein the waste pressure-sensitive adhesive product comprises a PET matrix and a pressure-sensitive adhesive layer, the pressure-sensitive adhesive layer comprises a copolyester elastomer, the copolyester elastomer is a copolymer of a carboxyl-terminated polyester and an amorphous carbon dioxide-based polyester diol, and the number-average molecular weight of the PET copolyester is 50,000 or below.

The invention discloses an anti-fouling curtain structure for water dredging engineering, and belongs to the technical field of environment protection of dredging engineering, the anti-fouling curtain structure for water dredging engineering comprises a floating body, an anti-fouling curtain and a vertical body, the floating body is arranged at the top end of the anti-fouling curtain, the vertical body is arranged at the bottom end of the anti-fouling curtain, and the anti-fouling curtain is geotechnical cloth; the geotechnical cloth is prepared from the following components in parts by weight: 100 to 150 parts of polyester, 20 to 50 parts of copolyester and 5 to 30 parts of inorganic filler, the copolyester is a copolymer of terephthalic acid, 5-sulfoisophthalic acid sodium salt, ethylene glycol and dihydroxyl-terminated polyvinyl imidazole, and the geotechnical cloth is further prepared by a post-treatment step. According to the invention, the copolyester composed of terephthalic acid, sodium 5-sulfoisophthalic acid, ethylene glycol and dihydroxyl-terminated polyvinyl imidazole and the inorganic filler are added into the polyester fiber, and the polyester fiber is modified through a post-treatment step, so that the alkali resistance and the antifouling property of the antifouling curtain are improved.

The invention relates to the technical field of high polymer materials, and discloses a preparation method of a modified master batch degradable material and application of the modified master batch degradable material in a packaging lunch box, and the modified master batch degradable material comprises the following components by mass: 75.0-93.8 parts of poly (butylene succinate); 5.0 to 20.0 parts of aliphatic series-aromatic copolyester; 1.0 to 4.0 parts of 1, 1 '-methylenebis-4, 1-phenylene-bismaleimide, and 1.0 to 4.0 parts of 1, 1'-methylenebis-4, 1-phenylene-bismaleimide; 0.5 to 2.0 parts of talcum powder; the method comprises the following steps: mixing dried poly (butylene succinate), aliphatic-aromatic copolyester, bismaleimide and talcum powder, performing reactive extrusion and melt mixing through a twin-screw extruder, and then cooling, pelletizing and drying the extrudate. Through specific components and a reactive extrusion process, a dynamic cross-linked network is formed by utilizing a Diels-Alder reaction, and the modified master batch degradable material of which the comprehensive mechanical property and the heat resistance are remarkably improved is prepared.

The invention relates to the field of polyester fiber production, and discloses modified copolyester, a preparation method thereof and a polyester fiber product. The modified copolyester contains a structural unit A as shown in a formula (I), a structural unit B as shown in a formula (II) and a structural unit C as shown in a formula (III), wherein R1, R2, R3 and R4 are each independently a C1-C10 alkyl group, and m is a positive integer greater than 3; rI, RII, and RIII are each independently hydrogen or a C1-C10 alkyl group. The preparation method comprises the following step: in the presence of a catalyst, carrying out contact reaction on a binary acid monomer, a dihydric alcohol monomer, a component a with a structure as shown in a formula (I), a component b with a structure as shown in a formula (II) and a component c with a structure as shown in a formula (III). The modified copolyester fiber material has good softness and crease resistance, the wearability of a polyester fiber product can be effectively improved, and the diversity and functionality of the polyester material are improved. # imgabs0 #

The present invention relates to a dental diaphragm copolyester and a preparation method thereof, the preparation method comprises the following steps: 2, 5-furandicarboxylic acid or an ester thereof, aliphatic or alicyclic diol and (2-hydroxy-5-formyl phenyl) diphenylborane are subjected to a reaction to obtain an esterification or ester exchange product; and carrying out condensation polymerization on the esterification or ester exchange product and the stabilizer to prepare the copolyester for the dental diaphragm. 2, 5-furandicarboxylic acid is derived from a renewable biomass resource and meets the requirements of green and sustainable development; compared with terephthalic acid and furan ring structures, the film has higher rigidity and polarity, the yield of hot press molding is improved, the same correction force can be met by a thinner film, the wearing comfort of a patient is improved, and meanwhile stress relaxation is improved; the catalyst perfectly combines strong Lewis acidity, intramolecular stabilization and potential bifunctional activation through structural design, provides possibility for efficient and green synthesis of polyester, avoids use of heavy metal, and is higher in biological safety.

The present invention discloses a method for preparing a recycled copolyester and a heat-shrinkable film thereof, belonging to the field of waste polyester recycling. The method utilizes technologies such as glycolysis and methanol transesterification of waste polyester to produce recycled dimethyl terephthalate, which is then transesterified with other modifying monomers and ethylene glycol, followed by polycondensation, to produce the recycled copolyester. Finally, the recycled copolyester is directly delivered to the extrusion dies via a melt delivery pipeline and a metering pump to produce the recycled polyester heat-shrinkable film. The recycled polyester heat-shrinkable film exhibits high shrinkage, excellent toughness, and transparency, while also achieving high-value recycling of waste polyester.

The invention relates to the field of bio-based composite materials, and discloses a bioplastic-based coupling agent, a modified bamboo fiber, a composite material and a preparation method and application of the bioplastic-based coupling agent and the modified bamboo fiber. The coupling agent is a product obtained by modifying polyhydroxybutyrate valerate and a grafting monomer, and the grafting monomer is at least one of maleic anhydride, acrylic acid or itaconic anhydride. The delignification bamboo powder is modified with the coupling agent, and the modified bamboo fiber, polyhydroxybutyrate-hydroxyvalerate, an initiator and an auxiliary agent are subjected to melt blending to obtain the composite material. The tensile strength and the bending strength of the composite material are respectively improved by 175% and 117%, and the crystallization ability and the thermal stability are also synchronously improved. According to the invention, the unification of high strength, thermal stability and excellent interfacial compatibility is realized while the degradability of the system is maintained, and the composite material has a good green composite material application prospect.

In one aspect, the present disclosure relates to a flame retardant plastic composition comprising a polymer component and a brominated flame retardant (BrFR), where the BrFR comprises one or more particles at least partially encapsulated by a thermoplastic toughening agent. In some aspects, the encapsulation can take the form of a core-shell structure wherein the shell has an average thickness of about 5 nm to 10 [mu] m. The thermoplastic toughening agent can be selected from the group consisting of styrenic block copolymers, thermoplastic polyurethanes, nitrile rubbers, acrylic elastomers, copolyester elastomers, thermoplastic polyether ester elastomers, thermoplastic amide ether elastomers, chlorinated rubbers, ionomers, thermoplastic vulcanizates, and combinations thereof. The flame-retardant plastic composition additionally comprises a filler and / or a compatibilizer. A method for preparing the flame retardant plastic composition and articles made from the composition are also disclosed.

The invention relates to the technical field of fabrics, in particular to a cool-feeling long cilia strip and a preparation method thereof.The cool-feeling long cilia strip is composed of cool-feeling fibers and a long cilia strip base material and is characterized in that the cool-feeling fibers comprise a core layer, a functional skin layer and an outer thin skin layer; the functional skin layer is prepared from the following components: a sulfonated copolyester matrix, catechol grafted master batch, surface modified zeolite nano powder, an anti-hydrolysis agent and an antioxidant, and the functional skin layer also contains introduced Zn < 2 + > and Mg < 2 + >. Zn < 2 + > and Mg < 2 + > which are stably combined on anchoring points of sulfonated copolyester are subjected to hydration endothermic reaction when being in contact with water, so that a cool feeling is generated; the surface modified zeolite nano powder synergistically enhances moisture absorption and water temporary storage by virtue of the specific surface area, and continuously provides water for an ionized hydration reaction to prolong and amplify a cool feeling effect; the catechol grafting structure endows the fiber with antibacterial performance, and long-term stability of the structure is ensured through an interface enhancement effect. And the outer layer hydrophilic polyester is matched, so that the product has comfort, durability and functionality.

The invention discloses a crystallinity low-melting-point polyester fiber and a preparation method thereof, and relates to the technical field of polyester fibers, the crystallinity low-melting-point polyester fiber is composed of a skin layer and a core layer, and a skin-core integrated crystallization design is adopted; the skin layer is modified copolyester, and the core layer is modified PET; the modified copolyester is prepared from the following raw materials in parts by weight: 38 to 42 parts of terephthalic acid, 12 to 15 parts of 2, 5-furandicarboxylic acid, 28 to 32 parts of 1, 4-cyclohexanedimethanol, 8 to 10 parts of polycaprolactone, 1.0 to 1.5 parts of a crystallization coordinating agent, 0.5 to 1.0 part of an antioxidant and 0.3 to 0.5 part of a hindered amine light stabilizer. The crystallization coordinating agent is prepared by compounding hydroxylated graphene and maleic anhydride grafted polyolefin elastomer according to a mass ratio of (2 to 3): 1. The fiber is good in high temperature resistance and durability, low in melting point, good in size stability and long in service life.

The present invention relates to a process for producing specialty polyesters and copolyesters from recycled bis-2-hydroxyethyl terephthalate (rBHET), which is derived from polyethylene terephthalate (PET) recovered from PET scrap or waste. The polyesters / copolyesters thus obtained are clean and high-quality and can be used in all applications, including but not limited to textiles, packaging, engineering, and industry.

The invention belongs to the technical field of high polymer material preparation, and provides a low-melting-point toughened copolyester chip and a preparation method thereof. The preparation method comprises the following steps: firstly, preparing hyperbranched polyester of which the surface is rich in carboxyl-terminated functional groups through core growth of polybasic acid alcohol and end group functionalization reaction of anhydride; the other chain extender is a linear chain extender which has a long flexible chain segment and two tail ends of which are also functionalized by carboxyl groups, and is obtained by carrying out end group esterification reaction on polyether glycol; then, in the synthesis process of the main polyester, carrying out multi-stage melt polycondensation on an aromatic dibasic acid component and a polyol component under the action of a composite catalyst system, introducing the hyperbranched polyester and a chain extender into a reaction system in the form of slurry, and covalently bonding a functional additive to a copolyester main chain through a polycondensation process, so as to obtain the hyperbranched polyester. An integrated network reinforced structure is formed, so that the copolyester chip has the characteristics of low melting point and excellent toughness.

A composite board, including a core, and a capstock positioned to at least partially cover the core, where the capstock includes 10 wt. % to 70 wt. % of polyvinyl chloride (PVC), based on a total weight of the capstock, 1 wt. % to 60 wt. % of acrylonitrile-styrene-acrylate (ASA), based on the total weight of the capstock, 1 wt. % to 60 wt. % of styrene-acrylonitrile (SAN), based on the total weight of the capstock, and 1 wt. % to 60 wt. % of a thermoplastic elastomer, where the thermoplastic elastomer includes styrene-isobutylene-styrene (SIBS), a thermoplastic copolyester elastomer, a polymeric plasticizer, and combinations thereof, wherein the capstock does not include thermoplastic polyurethane.

The invention provides isosorbide-based copolyester as well as a preparation method and application thereof, and relates to the technical field of high polymer materials. According to the preparation method, a step-by-step esterification method is adopted, firstly, isosorbide, excessive aromatic dicarboxylic acid and an acylating agent are subjected to a first esterification reaction, so that the acylating agent can efficiently and specifically activate secondary hydroxyl of isosorbide, and the initial esterification rate of isosorbide is greatly increased. Meanwhile, the excessive aromatic dicarboxylic acid ensures that the generated isosorbide prepolymer takes carboxyl as a terminal group, so that isosorbide molecules are'locked 'in the middle of a polymer chain segment. Due to the fact that the isosorbide is embedded in the middle of the chain segment in advance, the problem that the isosorbide falls off in the ester exchange reaction due to the fact that the isosorbide is located at the chain end and low in reaction activity in the subsequent polycondensation stage is effectively solved, and therefore the retention rate of the isosorbide in the final polymer is greatly increased, and the glass-transition temperature of the isosorbide is greatly increased.

Various aspects disclosed relate to a method of preparing a substantially sequence-uniform aliphatic copolyester. The method includes continuously contacting at least, a first monomer and a second monomer with an initiator and a catalyst to initiate ring-opening copolymerization of the first monomer and the second monomer. In the method the first monomer and the second monomer are contacted with the initiator and catalyst at a feed rate that is slower than a polymerization rate of the first monomer and the second monomer.

The invention discloses transparent copolyester, a preparation method thereof and a product prepared from the copolyester. The preparation method comprises the following steps: carrying out esterification or ester exchange reaction on dibasic acid or dimethyl ester of the dibasic acid and dihydric alcohol at 5-300kPaG to obtain an esterified substance or an ester exchange substance; then, the normal pressure of the system is recovered, the esterification or ester exchange temperature is kept unchanged, the negative pressure of the ester or ester exchange material is gradually reduced to high vacuum according to a certain pressure reduction rate, excessive monomers are removed, the content of impurities generated by the ester or ester exchange material is 0.3 wt% or below, and a prepolymer is obtained; and further heating the prepolymer, and carrying out final polycondensation reaction under high vacuum to obtain the target copolyester. The method can effectively weaken the side reaction in the synthesis process, improve the hue of the copolyester product, improve the light transmittance, reduce the haze and improve the heat resistance. Products prepared from the copolyester, such as bottle materials, sheets, plates and membrane materials, have the characteristics of light color, high transparency and good heat resistance.

The invention belongs to the technical field of high polymer materials, and discloses copolyester based on 4-aryl-epsilon-caprolactone and lactide as well as a preparation method and application of the copolyester. The copolyester is composed of a lactide structural unit and a 4-aryl-epsilon-caprolactone structural unit. A rigid benzene ring is introduced into a molecular chain, so that the synergistic balance of toughness and rigidity is successfully realized, and the toughness is remarkably improved while the high strength of the material is maintained. In addition, the introduction of phenyl endows the material with intrinsic ultraviolet resistance, the material can be used as an efficient ultraviolet absorbent, protective spherical protrusions are formed on the surface of the material under ultraviolet irradiation, and photooxidative degradation is effectively delayed. The material can be widely applied to the fields of high-performance degradable packaging, biomedical materials, outdoor articles, textiles and the like.

A composite board, including a core, and a capstock positioned to at least partially cover the core, where the capstock includes 10 wt. % to 70 wt. % of polyvinyl chloride (PVC), based on a total weight of the capstock, 1 wt. % to 60 wt. % of acrylonitrile-styrene-acrylate (ASA), based on the total weight of the capstock, 1 wt. % to 60 wt. % of styrene-acrylonitrile (SAN), based on the total weight of the capstock, and 1 wt. % to 60 wt. % of a thermoplastic elastomer, where the thermoplastic elastomer includes styrene-isobutylene-styrene (SIBS), a thermoplastic copolyester elastomer, a polymeric plasticizer, and combinations thereof, wherein the capstock does not include thermoplastic polyurethane.

The preparation method comprises the following steps: sequentially carrying out esterification reaction and polycondensation reaction on terephthalic acid, ethylene glycol, equol or a derivative thereof in the presence of the catalyst to generate the modified polyester, wherein the catalyst is prepared by enabling antimony trioxide, stannous octoate, tetrabutyl titanate and triphenyl phosphite to react in a solvent at the temperature of 100 DEG C or above; the modified polyester prepared by the method has relatively high intrinsic viscosity and fracture tensile strength, can meet the application requirements of special high polymer materials, and solves the problem that the application of semi-biomass PET copolyester in the field of special high polymer materials is limited in the prior art.

The invention relates to the technical field of biomedical materials, and discloses a degradable non-woven fabric and a preparation process thereof, the non-woven fabric is prepared from polylactic acid, polycaprolactone, periodate, a copolyester oligomer containing a cis-1, 2-cyclohexanediol structural unit, and a solid biocompatible weakly alkaline salt; the preparation process comprises the following steps: mixing the components, and performing melt blending and melt-blowing spinning to prepare the non-woven fabric. The periodate and the copolyester oligomer are used as latent reaction precursors, the alkalescent salt is used as a pH regulating agent, when the non-woven fabric is in contact with an aqueous environment, the alkalescent salt is dissolved out to establish an alkalescent microenvironment, the periodate is promoted to carry out oxidative cracking on the copolyester oligomer, and thus the aldehyde compound with antibacterial activity is generated in situ. According to the invention, the on-demand generation of antibacterial substances is realized, so that the non-woven fabric has high antibacterial rate and low cytotoxicity, and the technical problem that the activity and safety of a traditional antibacterial material are difficult to balance is solved.

The utility model belongs to the technical field of polymerization reaction kettles, and particularly relates to an anti-yellowing physical foaming PBT copolyester polymerization reaction kettle which comprises a bottom plate, a plurality of supporting frames are symmetrically arranged at the top end of the bottom plate, the supporting frames are L-shaped, mounting rings are arranged at the top ends of transverse frames of the supporting frames, an outer kettle body is arranged in the mounting rings, and the outer kettle body is arranged in the bottom plate. An inner kettle body is arranged in the outer kettle body, a fixing rod is arranged at the top end of the bottom plate, a chassis is arranged at the top end of the fixing rod, a material mixing assembly is arranged in the inner kettle body and comprises a rotating shaft, the rotating shaft is sleeved with a plurality of shaft sleeves, and a plurality of material mixing rods are arranged on the outer side walls of the shaft sleeves in a surrounding mode; a plurality of scrapers are arranged on the top end surface of the chassis, and a plurality of stirring rods are arranged on the outer side walls of the scrapers in parallel, so that materials can be uniformly mixed, the heat of the device can be preserved, and the materials react under proper conditions.

The invention provides a dental diaphragm with stress relaxation resistance as well as a preparation method and application thereof, and relates to the technical field of orthodontic materials. The dental diaphragm resistant to stress relaxation comprises a branched modified copolyester diaphragm, wherein the branched modified copolyester film is prepared from the following raw materials: terephthalic acid, alicyclic structure dihydric alcohol, side group dihydric alcohol and a polyfunctional group branching agent; wherein the glass transition temperature of the branched modified copolyester film is more than or equal to 80 DEG C, the light transmittance of the branched modified copolyester film is more than or equal to 86%, and the 24-hour tension attenuation rate of the branched modified copolyester film is less than or equal to 20%. The dental diaphragm provided by the invention has excellent tensile attenuation resistance, heat resistance and optical performance, is simple in processing technology, is more suitable for clinical requirements of dental orthodontic correction, and is particularly suitable for preparing dental orthodontic correction devices.

The invention belongs to the technical field of polymer materials, and particularly relates to a polyaromatic-carbonic acid-aliphatic copolyester production method which comprises the following steps: mixing aromatic dibasic acid and aliphatic dihydric alcohol, feeding into a first esterification kettle, and adding an esterification catalyst for esterification reaction to obtain an esterification product; uniformly mixing aliphatic dihydric alcohol, feeding the mixture into a second esterification kettle, adding diester carbonate and a transesterification catalyst into the second esterification kettle, reacting to obtain a transesterification product, and feeding the transesterification product into a demonomerisation kettle to obtain a demonomerisation product; mixing the esterification product and the demonomerisation product with a polycondensation catalyst and a stabilizer, shearing and homogenizing, feeding into a pre-polycondensation kettle for reaction to obtain a pre-polycondensation product, feeding the pre-polycondensation product into a final polycondensation kettle for reaction to obtain a copolymer, and performing water-cooling granulation to obtain a copolyester product. According to the production method provided by the invention, the final polycondensation time can be shortened, and the weight-average molecular weight and the mechanical strength of the prepared copolyester are improved.

A method of making a thermoplastic copolyester elastomer-based fiber is disclosed. The method comprises: providing a thermoplastic copolyester elastomer having a number average molecular weight of greater than 35,000 g / mol; and spinning the thermoplastic copolyester elastomer to provide a fiber comprising a spun thermoplastic copolyester elastomer, wherein the spun thermoplastic copolyester elastomer has a number average molecular weight that is 98% or less to 50% or more the number average molecular weight of the thermoplastic copolyester elastomer. A thermoplastic copolyester elastomer-based fiber made according to the aforementioned method and a fabric comprising the aforementioned thermoplastic copolyester elastomer-based fiber are also disclosed.