906 results about "Trans esterification" patented technology

The invention relates to a solvent-resistant medical connecting line sheath material and a preparation method thereof, and belongs to the technical field of high polymer materials. The sheath material is prepared from the following components: 38 to 44 weight percent of passivated toughening agent, 1.5 to 1.8 weight percent of heat stabilizer, 0.7 to 0.9 weight percent of lubricant, 0.12 to 0.15 weight percent of antioxidant and the balance of PVC (Polyvinyl Chloride) resin, the passivated toughening agent is prepared by the following steps: carrying out amine ester exchange reaction on 4-hydroxybutylamine and dimethyl difluoromalonate, introducing an alcohol-terminated hydroxyl group, carrying out substitution with dichloromethylvinylsilane to form a fluorine-containing chain compound, and finally carrying out double bond addition on methyl thioglycolate and a side chain; the passivation toughening agent is compatibilized through branched chain methyl ester and dynamically coordinated with a PVC molecular chain through a side chain thioether group, weakens the acting force between PVC chains, plays a good toughening role, inhibits dissolution through physical crosslinking, shields and passivates the PVC molecular chain, and relieves swelling of PVC in a solvent.

The invention relates to a kitchen waste oil recovery treatment method, which comprises: S1, carrying out multi-field synergistic pretreatment: sequentially carrying out ultrasonic wave and high-frequency pulse electric field treatment on waste oil to break an emulsion layer, adding magnetic nanoparticles to adsorb polar impurities, and carrying out magnetic field separation to obtain high-purity oil; s2, supercritical catalytic reaction: under the CO2 supercritical condition, using a core-shell structure composite catalyst to synchronously perform transesterification reaction and glycerol dehydration reaction; s3, dynamic membrane separation: separating biodiesel and glycerol in real time through an intelligent membrane assembly; s4, gradient utilization of energy: recovering reaction waste heat to drive membrane distillation to concentrate wastewater, and using tail gas CO2 for carbonation reaction to generate calcium carbonate. Through four core technologies of multi-field collaborative pretreatment, low-temperature supercritical catalysis, dynamic membrane separation and energy gradient utilization, triple limitations on efficiency, cost and environmental protection in the prior art are remarkably broken through.

The invention discloses a method for preparing regenerated flame-retardant high-shrinkage polyester by a methanol alcoholysis method, and belongs to the technical field of polyester. The method comprises the following steps: (a) mixing the waste polyester fabric with methanol, and carrying out catalytic depolymerization to obtain a regenerated DMT mixed solution; (b) carrying out impurity separation and methanol recovery treatment on the regenerated DMT mixed solution, and then carrying out cooling crystallization, centrifugal drying and rectification purification treatment to obtain pure DMT; (c) carrying out transesterification on pure DMT, ethylene glycol, a transesterification catalyst and a DEG inhibitor; (d) after the ester exchange reaction, adding CEPPA-EG and IPA-EG for copolymerization; adding a polymerization catalyst, a stabilizer and an antioxidant for polymerization reaction to obtain a modified polyester melt; and (e) granulating and drying to obtain the slices. The regenerated polyester prepared by the method has multiple functions of flame retardance, high boiling water shrinkage, low-temperature dyeing and the like, and is suitable for the fields of high-end clothing, automotive trim, electronic packaging materials and the like.

The invention provides a preparation method of mannitol carbonic acid sulfate, mannitol and dimethyl carbonate are used as starting raw materials to prepare mannitol carbonic acid sulfate, a target compound is obtained through ester exchange, cyclization and oxidation reaction, the raw materials are low in price and easy to obtain, the reaction operation is simple and convenient, the yield of the obtained product is 81% or above, the purity is 99.6% or above, and the method is suitable for industrial production. The method is suitable for industrial production.

The invention discloses a reprocessable solid-solid phase change material based on dynamic borate bonds and a preparation method of the reprocessable solid-solid phase change material. Based on the mechanism that boric acid ester is subjected to ester exchange during thermal stimulation, a dynamic cross-linking agent containing boric acid ester is adopted for cross-linking a polyurethane prepolymer, polyethylene glycol is cross-linked through chemical bonds, the tensile strength and the elongation at break of the phase change material are improved, and the problem that the phase change material is prone to leakage in the phase change process is solved; besides, borate bonds belong to associated dynamic covalent bonds and can keep the crosslinking density of the material unchanged when ester exchange occurs under thermal stimulation, so that the thermal stability of the material is relatively good; the solid-solid phase change material disclosed by the invention is excellent in mechanical property, has a relatively high enthalpy value, can be reprocessed, and has an application prospect in the fields of thermal management, energy storage, infrared stealth and the like.

The invention relates to a preparation method and application of a three-step method environment-friendly SBS modified asphalt regenerant, and the regenerant is composed of modified bio-oil, functionalized desulfurized rubber, a solubilizer, an anti-oxidation aging agent, an anti-light aging agent, a multi-sulfydryl chain reconstruction auxiliary agent, a reversible thioether cross-linking agent and other components. The matrix and polymer network structure of the aged SBS modified asphalt is repaired through light oil supplement and chemical reaction. The preparation method comprises the following steps: introducing a polar functional group into ultrasonic transesterification modified bio-oil to improve wettability; the surface activity of the desulfurized rubber is improved through plasma low-temperature treatment; high-speed shearing and closed-loop control reaction are combined to realize rubber particle dispersion and network reconstruction; chemical crosslinking and aging regeneration are realized through cooperation of specific components. The prepared regenerant is doped into aged SBS modified asphalt at the temperature of 145-165 DEG C according to the proportion of 4-20 wt% to prepare regenerated asphalt.

The invention relates to the technical field of high polymer materials, in particular to a low-warpage PBT / PC composite modified material and a preparation method thereof. The composite material is prepared from the following raw materials: PBT resin, PC resin, a filler, an ester exchange inhibitor, a flexibilizer, a compatilizer, an antioxidant, a lubricant, a flowable agent and glass fibers. The preparation process comprises the steps of resin drying and mixing, additive premixing, melt blending extrusion and the like, is simple and controllable in flow and is suitable for large-scale production. The composite material prepared by the invention has high strength, high toughness, low warping degree and excellent processability, can be used for ultrasonic welding, reduces after-shrinkage of the material, solves the problem of melt cooling film sticking, and meets the requirements of the market on high-precision and high-stability engineering plastics.

The invention belongs to the technical field of polyester polyol, and particularly relates to high-functionality low-viscosity polyester polyol and a step-by-step synthesis method thereof. Comprising the following steps: (1) adding dihydric alcohol, dicarboxylic acid, a catalyst and an antioxidant into a reaction kettle, heating and vacuumizing, and carrying out esterification and ester exchange reaction to prepare a polyester polyol intermediate; and (2) cooling the polyester polyol intermediate prepared in the step (1), adding polyol into the reaction kettle, and continuously carrying out ester exchange reaction to obtain the high-functionality low-viscosity polyester polyol after the reaction is finished. According to the step-by-step synthesis method, the problems that in the prior art, high-functionality polyester polyol is large in viscosity and low-viscosity products are difficult to prepare are solved, the viscosity of the high-functionality polyester polyol can be effectively reduced under the same raw material system and hydroxyl value conditions through specific raw material selection and process control, and the method is simple in process and easy to implement. The industrial production is convenient.

The invention relates to the technical field of organic synthesis, in particular to a method for homogeneous catalytic synthesis of dimethyl carbonate by using a liquid separation method to separate a catalyst, which comprises the following steps: by using 0.3-15% long-chain tertiary amine as a homogeneous catalyst, carrying out homogeneous reaction on cyclic carbonate and methanol in a mass ratio of 1: (1.2-5.5) at 60-80 DEG C for 4-7 hours. And after the homogeneous transesterification reaction is completed, carrying out atmospheric distillation on the reaction mixture, and collecting fractions to obtain the target product dimethyl carbonate. Carrying out liquid separation on the heterogeneous atmospheric distillation residual liquid, and collecting a lower-layer material to obtain a by-product; and the collected material is a catalyst which can be directly recycled subsequently. The dimethyl carbonate synthesis method provided by the invention has the characteristics of high catalytic efficiency, easy catalyst separation, environmental protection, energy saving and the like.

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 relates to the technical field of immobilized lipase, in particular to immobilized lipase taking modified nano SiO2 as a carrier as well as a preparation method and application of the immobilized lipase. The immobilized lipase sold in the market is high in price and poor in mechanical strength, the enzyme loss is too large due to shear force or carrier structure damage in the continuous production process, and the transesterification efficiency is poor. In order to solve the technical problems, the invention provides the immobilized lipase taking the modified nano SiO2 as the carrier, the immobilized lipase is obtained by sequentially grafting a modified nano silicon dioxide carrier with an amino silane coupling agent and an epoxy silane coupling agent and loading lipase on the surface of the modified nano silicon dioxide carrier, according to the method, the immobilized lipase forms an enzyme column in a chromatographic column and then serves as a reactor, damage of mechanical stirring to lipase particles is avoided, the ester exchange degree is more effectively controlled by adjusting the flow speed of a substrate, the production cost of an enterprise can be remarkably reduced, and the product quality is improved.

The invention belongs to the technical field of chemical production, and particularly relates to high-purity dimethyl carbonate and a preparation method thereof. The preparation method comprises the following steps: taking ethylene carbonate and methanol as raw materials, taking an alkali alcohol solution as a catalyst, carrying out transesterification in a rectifying tower to obtain dimethyl carbonate and methanol azeotrope, and extracting the azeotrope from the top of the rectifying tower; separating the dimethyl carbonate and methanol azeotrope by adopting pressurized azeotropic distillation to obtain a dimethyl carbonate crude product; and conveying the dimethyl carbonate crude product into a falling film crystallizer for continuous falling film crystallization, controlling the temperature of low-temperature chilled water in the falling film crystallizer to be-10 to 2 DEG C and the circulating material amount to be 3-5 times of the mass of the product required to be produced, and heating to melt the material to obtain the high-purity dimethyl carbonate product. According to the preparation method provided by the invention, rectification crude purification and continuous falling film crystallization processes are adopted, and dimethyl carbonate with the purity of 99.99% or above is obtained.

The invention relates to a preparation method and system of high-molecular-weight polyethylene glycol oxalate, and the preparation method comprises the following steps: adding oxalic acid diester, ethylene glycol and a first catalyst, and carrying out transesterification to obtain an ester; adding a second catalyst, and carrying out a pre-polycondensation reaction on the esterified product to obtain a glycol oxalate oligomer; polymerizing the ethylene glycol oxalate oligomer, and carrying out final polymerization reaction to obtain polyethylene glycol oxalate; the molar ratio of the oxalic acid diester to the ethylene glycol is (1.05-1.3): 1. Compared with the prior art, by controlling excessive oxalic acid diester in the raw material ratio, namely controlling the molar ratio of oxalic acid diester to ethylene glycol to be greater than 1, the reaction rate of ethylene glycol is improved, self-polycondensation of ethylene glycol is prevented, further increase of molecular weight is facilitated, and meanwhile, the thermal performance of the product is improved.

The invention relates to the technical field of polyester fibers, in particular to a negative ion polyester fiber which is prepared from the following raw materials in percentage by mass: 85-92% of polyethylene glycol terephthalate, 3-8% of nano tourmaline composite powder, 2-5% of a titanium dioxide / graphene composite carrier, 0.5-1.5% of a coupling agent and 0.3-0.8% of an antioxidant. The invention also discloses a preparation method of the composition. According to the invention, the core-shell structure optimization design is adopted, the core layer ensures the high loading capacity of the tourmaline composite powder, the shell layer has the synergistic effect of the titanium dioxide / graphene composite carrier, the negative ion release efficiency is obviously enhanced, the particle size of the nanoscale tourmaline is controlled to be 50-100nm, the nanoscale tourmaline is uniformly dispersed, the nanoscale tourmaline and graphene form a heterojunction structure, and the electron transmission capability is greatly improved; the negative ion release amount meets the JIS standard, a chemical bonding interface is formed through transesterification, the structural stability is enhanced, and the retention rate of the negative ion release performance is still high even after multiple times of washing.

The invention belongs to the technical field of polyester master batches, and particularly relates to a damp-heat-resistant ultraviolet barrier polyester master batch and a preparation method thereof. The invention discloses an anti-ultraviolet polyethylene glycol terephthalate composite material, which is prepared from the following raw materials in parts by weight: 85 to 90 parts of polyethylene glycol terephthalate, 10 to 15 parts of anti-ultraviolet agent, 3 to 5 parts of epoxy-terminated polyether and 1 to 3 parts of lubricant, wherein the anti-ultraviolet agent is a modified intermediate obtained by modifying a nano light screening agent by a carboxylic ester coupling agent according to a mass ratio of (3 to 5): 100; the modified intermediate and a hydroxybenzophenone derivative are subjected to a grafting reaction according to the mass ratio of 100: (5-8); the nano light screening agent is selected from one or a combination of two or more of nano zinc oxide, nano titanium dioxide, nano cerium oxide, nano tin antimony oxide and nano carbon black. The dispersion effect of the anti-ultraviolet agent in the master batch is improved, and the ultraviolet barrier and the light transmittance are improved; meanwhile, the anti-ultraviolet agent is subjected to ester exchange with PET in the screw extrusion process, so that the interaction with PET is enhanced, migration in a humid and hot environment is avoided, and the ultraviolet shielding performance is lasting and stable.

The invention relates to the field of chemical synthesis, in particular to a production process of allyl diethylene glycol dicarbonate, which comprises the following steps: by taking allyl alcohol and dimethyl carbonate as raw materials, carrying out transesterification under the action of a core-shell catalyst to generate dipropylene carbonate; carrying out solid-liquid separation, carrying out reduced pressure distillation to recover methanol and dimethyl carbonate, and then carrying out second-step ester exchange reaction with diethylene glycol under the action of the same catalyst to generate allyl diethylene glycol dicarbonate; and finally, performing multi-stage reduced pressure distillation purification to obtain a high-purity product. According to the core-shell type catalyst, an MCM-41 molecular sieve is used as a carrier, an inner core is formed after amino modification and zirconium ion coordination, then an interface layer and a phenyl modified silicon dioxide shell are used for packaging, and the core-shell type catalyst has high activity, high selectivity and excellent structural stability. The method has the advantages of mild process conditions, recyclable catalyst, high product yield and excellent purity, and is suitable for industrial production.

The invention relates to the technical field of polymer dye synthesis, in particular to a polymer coloring agent based on a binary acid chromophoric monomer, a color master batch, a fiber and a preparation method of the polymer coloring agent. The structural formula of the diacid chromophoric monomer is as follows: # imgabs0. The chromophoric monomer has extremely high thermal stability, and can maintain the chemical structural integrity and chromophoric performance in a high-temperature environment (250 DEG C). The heat-resistant characteristic is mainly derived from a highly stable aromatic skeleton formed by a parent nucleus through an expanded conjugated system and a rigid plane structure, and heat vibration energy is effectively dispersed; in addition, a thermal stable group (an all-carbon skeleton) is introduced through side chain modification to form a steric hindrance effect, and molecular movement at high temperature is inhibited. Due to the unique heat resistance of the monomer, the monomer can be completely matched with a high-temperature processing window (240-300 DEG C) of a polyester melt polymerization process, and a polymer-dye composite system with a stable structure is constructed through covalent bonding in ester exchange and polycondensation processes.

The invention relates to the field of polyurethane, and discloses a preparation method of a linear reaction type phosphorus-nitrogen-silicon synergistic flame-retardant solvent-free polyurethane coating, which comprises the following steps: S1, carrying out exchange reaction on phosphonate and alcohol amine ester to obtain a phosphorus-nitrogen polyol intermediate; s2, carrying out condensation polymerization on the phosphorus-nitrogen polyol intermediate and chlorosilane to obtain phosphorus-nitrogen-silicon polyol; s3, mixing polyester / polyether polyol, a chain extender and an amine / metal catalyst to obtain a component A; mixing and reacting isocyanate, part of polyester / polyether polyol and phosphorus-nitrogen-silicon polyol to obtain a component B; mixing the component A and the component B, spraying the mixture on release paper, and curing. Through a synergistic flame-retardant mechanism of phosphorus, nitrogen and silicon, the balance of efficient flame retardance, mechanical properties and excellent coating properties is realized. The solvent-free system realizes zero emission of volatile organic compounds, and the linear reaction type design ensures that the mechanical properties and durability of the coating are not influenced.

The invention belongs to the technical field of polymer composite materials, and particularly relates to a polycarbonate modified composite material as well as a preparation method and application thereof, and the polycarbonate modified composite material comprises 60-85 parts of a PC base material, 10-30 parts of a bio-based monomer, 1-8 parts of surface modified nano cellulose and 0.1-2 parts of a transesterification catalyst. According to the polycarbonate modified composite material as well as the preparation method and the application thereof provided by the invention, chemical bonding of a bio-based monomer and a PC main chain is realized through transesterification, phase separation is avoided, and the core pain point of traditional blending modification is solved; the biodegradation rate is increased by 30% or above compared with pure PC, and meanwhile, the excellent mechanical properties (the tensile strength is larger than or equal to 60 MPa, and the notch impact strength is larger than or equal to 5 kJ / m) of PC are reserved; the melt flow rate is increased by more than 25%, the processing energy consumption is reduced, and the application scene is widened; the carboxylic acid modified nano cellulose and the block copolymer form a synergistic network, so that the mechanical property, the thermal stability and the degradation uniformity are synchronously improved.

The invention provides an epoxidized soybean oil-binary acid bio-based dynamic polymer, a preparation method thereof and a paper-based strain sensor packaged by the epoxidized soybean oil-binary acid bio-based dynamic polymer. The preparation method of the dynamic polymer comprises the following steps: (1) taking epoxidized soybean oil as an epoxy monomer, aliphatic dibasic acid as a flexible monomer and aromatic dibasic acid as a rigid monomer, and carrying out polymerization reaction in the presence of a transesterification catalyst to obtain a dynamic polymer prepolymer; the aliphatic binary acid comprises succinic acid, adipic acid and sebacic acid; (2) removing bubbles from the dynamic polymer prepolymer; and (3) carrying out thermal curing on the dynamic polymer prepolymer to obtain the epoxidized soybean oil-binary acid bio-based dynamic polymer. The epoxidized soybean oil-binary acid bio-based dynamic polymer has good mechanical properties and hydrophobicity, a paper-based strain sensor based on the epoxidized soybean oil-binary acid bio-based dynamic polymer also has good mechanical properties and hydrophobicity, and the sensor has certain application potential in the field of human motion monitoring.

Provided are industrial processes for producing an organic acid alky ester from a feedstock containing organic acids and / or saponifiables, comprising: countercurrently contacting a feedstock with an organic alkylating reagent over two or more vessels or stages at temperature between 100° C. and 400° C. and pressure between 0.1 barg and 355 barg while simultaneously removing water and / or glycerin with unreacted alkylating reagent from the final vessel or stage to result in a first reaction method product containing organic acid alkyl esters, followed by a choice of using the alkyl esters as-is, purifying the organic acid alkyl esters from the first reaction product mixture or subjecting the first reaction product mixture to an additional transesterification reaction to convert saponifiables into additional organic acid alkyl esters, then purifying the organic acid alkyl esters from this second reaction method product.

According to the method, industrial-grade 1, 2-propylene glycol co-produced by a dimethyl carbonate process through a transesterification method is taken as a raw material, and purification processes of activated carbon adsorption impurity removal, deodorant impurity removal and rectification impurity removal are carried out, so that various indexes such as chromaticity, odor, purity and ultraviolet light transmittance of the obtained 1, 2-propylene glycol product reach the quality indexes of an imported pharmaceutical-grade 1, 2-propylene glycol product. According to the method disclosed by the invention, the pharmaceutical grade propylene glycol can be prepared with high quality, and a good development prospect and huge economic benefits are undoubtedly brought to the propylene glycol industry.

The invention relates to a preparation method of an epoxy coating, in particular to a preparation method of an epoxy coating with self-repairing performance, which is a self-repairing epoxy coating based on the synergistic effect of siloxane modified graphene oxide (GOS) and boron-oxygen-containing six-ring modified polydimethylsiloxane (BP-AMINE). The preparation method comprises the following steps: grafting (3-aminopropyl) triethoxysilane to graphene oxide through a chemical condensation method to prepare GOS, and preparing a BP-AMINE monomer through a chemical substitution method. The coating is endowed with quick self-repairing capability by utilizing reversibility of siloxane exchange reaction of GOS and boron oxygen hexacyclic ester exchange reaction of BP-AMINE. The coating can be repaired within 30 minutes at the temperature of 70 DEG C after being scratched, the repairing efficiency is larger than or equal to 98%, the repaired coating still keeps excellent corrosion resistance after being soaked in a 3.5 wt% NaCl solution for 60 days, and the coating is suitable for the fields of metal protection, aerospace and the like.

The invention relates to a mildew-proof and odor-resistant textile material produced from conjugated fibers and a preparation method of the mildew-proof and odor-resistant textile material, and belongs to the technical field of textiles. According to the invention, the antibacterial color fixing agent is prepared, the antibacterial color fixing agent is used for carrying out ester exchange modification on PTT to obtain the modified PTT master batch, and then the master batch is used as an'island 'component to prepare the sea-island conjugated fiber, so that the technical defect that a functional auxiliary agent is dissolved in a solvent together with the'sea' component when the sea-island conjugated fiber is prepared is effectively overcome; the sea-island conjugated fiber textile material has good antibacterial performance, still has good retention rate after being washed with water, has good moisture regain and color fastness, is skin-friendly and breathable, and effectively improves the wearing comfort of the PTT-based textile material.

The polyester resin is described, which has repeating units derived from a diester component of a dicarboxylic acid; and a diol component. The diester of the aliphatic dicarboxylic acid includes a succinic acid diester, the diol component comprises 50 to 100 mol % of an anhydrosugar alcohol, based on 100 mol % of the total diol component, and the number average molecular weight (Mn) of the polyester resin is 10,000 g / mol or more. A method for preparing a polyester resin comprises (1) esterification or transesterification of a diester component of a dicarboxylic acid comprising a diester of an aliphatic dicarboxylic acid and a diester of an aromatic dicarboxylic acid and a diol component comprising an anhydrosugar alcohol; and (2) polycondensation of the reaction product obtained in step (1). The polyester resin has excellent heat resistance and mechanical properties and also has excellent biodegradability.

The invention discloses a reversible cross-linked paper coating and a repulping switching process, and belongs to the technical field of paper coatings. The coating is composed of an acrylate emulsion, a polyhydroxyalkanoate dispersion and a dynamic cross-linking system, wherein the system is one of carbonyl-hydrazine, imine, Diels-Alder, ester exchange, borate or polyvalent metal-carboxylate. The coating is coated with 6-15 g / m, the use state is that Cobb60 is smaller than or equal to 18 g / m, Kit is larger than or equal to 10, WVTR is smaller than or equal to 80 g / (m.d) at the temperature of 38 DEG C and the RH of 90%, OTR is smaller than or equal to 200 cm / (m.d) at the RH of 23 DEG C / 80%, the initial sealing temperature is smaller than or equal to 180 DEG C, and the sealing strength is larger than or equal to 6.0 N / 15 mm. In the re-pulping stage, net releasing is triggered through alkali, acid (containing CO2 injection), a chelating agent or ultrasonic assistance, and according to CEPI V3 / PTS-RH 021: 2012, the fiber recovery rate is measured to be larger than or equal to 98%, the coarse slag rate is measured to be smaller than or equal to 1.0%, and the adhesion matter is measured to be smaller than or equal to grade 1. The formula does not contain PFAS, and high bio-based carbon content can be realized.

The invention relates to the technical field of rubber production, and discloses a micro-nano cellulose reinforcing filler, a preparation method thereof and a cellulose-rubber composite material. The preparation method of the micro-nano cellulose reinforcing filler comprises the following steps: carrying out oxidation treatment on cellulose to obtain modified cellulose with carboxyl functional groups; and carrying out transesterification on the modified cellulose and an unsaturated ester compound to obtain the micro-nano cellulose reinforcing filler. The method does not need traditional homogenization treatment, and is low in energy consumption and high in yield; the hydrogen bond acting force between cellulose molecules is reduced, the aggregation of the nano cellulose caused by hydrogen bonds can be effectively prevented, and the preparation process is simplified. The cellulose reinforcing filler prepared by the invention is a nanoscale cellulose sheet, and has high dispersity and good compatibility in polar rubber; high fraction filling can be realized, the thickness of an interface layer is improved, and external stress is effectively dissipated; the prepared cellulose-rubber composite material is low in compression temperature rise and rolling resistance and excellent in wet skid resistance.

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 application provides a hindered amine light stabilizer and a preparation method thereof, and the preparation method comprises the following steps: putting N, N-bis(2, 2, 6, 6-tetramethyl-4-piperidyl) 1, 6-hexanediamine and an organic solvent into a reaction bottle, heating to 50-80 DEG C, adding methyl acrylate into the system dropwise, obtaining an intermediate I through an addition reaction, and then obtaining a crude product through an ester exchange reaction of the intermediate I and tetramethylpiperidinol in the presence of a catalyst and an organic solvent, washing with water, decoloring, filtering, cooling and crystallizing, filtering and drying to obtain the product; the light stabilizer obtained by the application has multiple hindered amine functional groups, has good heat resistance and extraction resistance, and has good compatibility with resin.

The invention relates to the technical field of polymer dye synthesis, and discloses a monomer for a blue polyester fiber and a preparation method thereof.According to the monomer for the blue polyester fiber, 1, 4-arylamino substituted anthraquinone serves as a color development mother nucleus, a benzoate group is introduced to aryl of the 1, 4-arylamino substituted anthraquinone mother nucleus, and the monomer for the blue polyester fiber is obtained; the benzoate group is connected with the chromophoric parent nucleus through a carbon-carbon bond; the molecular terminal of the monomer for the blue polyester fiber is connected with an exposed ester group through an aryl group, and the exposed ester group is used for transesterification with dihydric alcohol under the melt polycondensation condition of polyester. The novel monomer for the blue polyester fiber, provided by the invention, has excellent color development performance and thermal stability, can be directly used for in-situ synthesis of blue polyester and can be directly used for melt spinning, and the color fastness and coloring uniformity of a product are improved; meanwhile, the monomer for the blue polyester fiber, provided by the invention, is simple in preparation method, low in cost and easy for large-scale production.