WO2007134550A1 - A method for preparing nylon microsphere and the same - Google Patents
A method for preparing nylon microsphere and the same Download PDFInfo
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- WO2007134550A1 WO2007134550A1 PCT/CN2007/070038 CN2007070038W WO2007134550A1 WO 2007134550 A1 WO2007134550 A1 WO 2007134550A1 CN 2007070038 W CN2007070038 W CN 2007070038W WO 2007134550 A1 WO2007134550 A1 WO 2007134550A1
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G69/00—Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
- C08G69/02—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids
- C08G69/08—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids derived from amino-carboxylic acids
- C08G69/14—Lactams
- C08G69/16—Preparatory processes
- C08G69/18—Anionic polymerisation
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G69/00—Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
- C08G69/46—Post-polymerisation treatment
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G69/00—Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
- C08G69/02—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids
- C08G69/08—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids derived from amino-carboxylic acids
- C08G69/14—Lactams
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G69/00—Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
- C08G69/02—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids
- C08G69/08—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids derived from amino-carboxylic acids
- C08G69/14—Lactams
- C08G69/16—Preparatory processes
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J3/00—Processes of treating or compounding macromolecular substances
- C08J3/12—Powdering or granulating
- C08J3/14—Powdering or granulating by precipitation from solutions
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J3/00—Processes of treating or compounding macromolecular substances
- C08J3/02—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques
- C08J3/09—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques in organic liquids
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L77/00—Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
- C08L77/02—Polyamides derived from omega-amino carboxylic acids or from lactams thereof
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/582—Recycling of unreacted starting or intermediate materials
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2982—Particulate matter [e.g., sphere, flake, etc.]
Definitions
- This invention relates to a method of making nylon microspheres and nylon microspheres. More specifically, the present invention relates to a process for preparing high molecular weight nylon microspheres of controlled particle size, and nylon microspheres having a high molecular weight and a controlled particle size. Background technique
- Nylon has high strength, high wear resistance, high chemical resistance, good resistance to deformation and aging, and has a wide range of applications in engineering plastics.
- the molecular weight of the nylon synthesized by the anionic ring-opening polymerization method is much higher than that of the nylon synthesized by the polycondensation method, and thus has more advantages in application.
- Nylon granules have broad application prospects in coatings, rotational molding materials and extrusion molding materials.
- Conventional preparation methods of nylon granules include: solution precipitation method, emulsion method, direct polymerization method and mechanical pulverization method (low temperature, slicing method and jet pulverization method).
- the above preparation methods generally have the defects of complicated technology, high cost and energy consumption, irregular shape of the granular powder, large particle size and wide distribution range, which brings great difficulties to practical applications.
- Patent WO03097228 proposes a process for the preparation of polyamide particles by interfacial polycondensation.
- the above two preparation methods are complicated in process, require a large amount of solvent and dispersant, and are not suitable for industrialization.
- Patent CN1624025 a method for blending polyamide pellets and water-soluble polymer, synthesizing polyamide as dispersed phase, water-soluble polymer as continuous phase blend, and then removing water-soluble polymer with water to obtain polyamide powder is proposed.
- this method is advantageous for industrial production, the raw material used is polyamide powder, and the preparation of the polyamide powder requires a large amount of energy consumption. Summary of invention
- Still another object of the present invention is to provide a nylon microsphere having a high molecular weight and a controlled particle size.
- a method of preparing a nylon microsphere characterized in that The method includes the following steps (1), (2), and (3) or includes the following steps ( ⁇ ), (2), and (3):
- the radical polymer is soluble in the lactam monomer; the radically polymerizable monomer is selected from those formed by a free radical polymer capable of dissolving in the One or more monomers of the lactam monomer.
- the free-radically polymerizable monomer is one or more selected from the group consisting of acrylate, methacrylate, acrylamide, acrylonitrile, styrene, methyl styrene, vinyl Pyrrolidone, vinyl acetate, divinylbenzene, and derivatives thereof; the radical polymer is a homopolymer of one of the above monomers or a copolymer of two or more monomers.
- the radically polymerizable monomer is used in an amount of 5 to 80% by weight, based on the radical polymerizable monomer and the lactam monomer.
- the radical polymer is used in an amount of 5 to 80% by weight based on the total weight of the radical polymer and the lactam monomer.
- the radically polymerizable monomer is used in an amount of 10 to 50% by weight, based on the total weight of the radical polymerizable monomer and the lactam monomer; in the step ( ⁇ ) The radical polymer is used in an amount of 10 to 50% by weight based on the total weight of the radical polymer and the lactam monomer.
- the lactam monomer is one or more selected from the group consisting of C 4 -C 12 lactams; when the lactam monomer is one, the polyamide is the lactam single A homopolymer of a body; when the lactam monomers are two or more, the polyamide is a copolymer of these lactam monomers.
- the free radical polymerization of step (1) is carried out in the range of from 60 to 150 °C.
- the anionic ring opening polymerization of step (2) is carried out in the range of from 120 to 250 °C.
- the anionic ring opening polymerization process of the lactam monomer is selected from the group consisting of a static casting process or a reactive extrusion process.
- the radical initiator is one or more selected from the group consisting of an azo initiator, an organic peroxy initiator, and an oil-soluble oxidation-reduction. Initiating system; the free radical initiator is present in an amount of from 0.05 to 5% by weight based on the total weight of the free radical polymerizable monomer and the lactam monomer.
- the initiator is selected from the group consisting of a lactam metal compound, an alkali metal, an alkali metal hydride, an alkali metal hydroxide, an alkali metal alkoxide or an alkali metal carbonate.
- the activator is one or more selected from the group consisting of substituted or unsubstituted isocyanates, acetyl caprolactams, acid chlorides or acid anhydrides.
- the initiator is one or more selected from the group consisting of sodium, sodium, potassium, lithium, NaH, LiH, NaOH, KOH or Na 2 CO 3 .
- the particle size of the nylon microspheres is controlled by adjusting the ratio of the amount of free radical polymer to lactam monomer.
- the free radical polymer removed by dissolution in step (3) is recovered, and the recovered radical polymer is mixed with the molten lactam monomer to provide the freedom described in the step ( ⁇ ).
- the mixture of the base polymer and the lactam monomer continues to produce nylon microspheres by carrying out steps (2) and (3).
- a nylon microsphere characterized in that the weight average molecular weight of the nylon is in the range of 10,000 to 300,000, and the particle diameter of the nylon microsphere is in the range of 0.1 to 500 ⁇ m.
- the nylon has a weight average molecular weight in the range of 10,000 to 80,000 and the nylon microspheres have a particle diameter in the range of 0.5 to 100 ⁇ m.
- the nylon has a weight average molecular weight in the range of 25,000 to 60,000, and the nylon microspheres have a particle diameter in the range of 1 to 50 ⁇ m.
- the nylon is a monomer of the amide 4 -c 12 c is selected from a homopolymer or a copolymer of two or more monomers.
- FIG. 1 is a scanning electron microscope (SEM) photograph of a nylon 6 microsphere obtained in Example 1 of the present invention, at a magnification of 100 times. Detailed description of the invention
- a major feature of the present invention is the preparation of a polymer alloy of a free radical polymer/polyamide by continuous in-situ polymerization by free radical polymerization and anionic ring opening polymerization, respectively.
- This system utilizes lactam as a solvent for the radical polymerizable monomer, and the radical polymerization monomer and the lactam monomer are separately polymerized in situ by continuous solution radical polymerization and anion ring-opening polymerization to obtain an alloy of the two.
- many free radical polymers do not themselves dissolve in the lactam monomer, so the polymer alloy of the free radical polymer/polyamide cannot be obtained by in situ anionic ring opening polymerization.
- the radical polymer/lactam monomer mixture obtained by radical polymerization is a transparent and stable system, and the presence of the radical polymer does not affect the anion of the lactam monomer. Ring opening polymerization.
- Another major feature of the present invention is also that the key to the present invention is the use of spherical nylon particles having a substantially regular shape.
- high levels of polymer are present in the form of a continuous phase, while low levels of polymer are present in the form of a dispersed phase.
- Reverse rotation means a state in which a low content of a polymer is a continuous phase and a high content of a polymer is a dispersed phase.
- polyamide (nylon;) is the structure of the dispersed phase.
- the polyamide exists in a spherical state due to factors such as viscosity and interfacial tension, and the radical polymer exists between the ball of the polyamide phase and the gap between the balls.
- the polyamide phase exists in a state of a regular spherical shape.
- the nylon microspheres having a regular spherical shape can be obtained by dissolving the radical polymer in a suitable organic solvent, washing and drying.
- the size of the nylon microspheres can be controlled by adjusting the ratio of the amount of free radical polymer to lactam monomer.
- the ratio of the amount of the radical polymer to the lactam monomer is small, the size of the obtained nylon microspheres is large.
- the ratio of the amount of the radical polymer to the lactam monomer increases, the size of the obtained nylon microsphere becomes small.
- the concentration of the initiator and the activator (based on the lactam) is low, and the obtained nylon has a large molecular weight; and as the concentration of the initiator and the activator increases, the molecular weight of the obtained nylon becomes smaller. . Therefore, by adjusting the concentration of the initiator and the activator in the lactam polymerization process, the molecular weight of the nylon microspheres can be controlled.
- a mixture of a radical polymer and a lactam monomer can be obtained by one of two methods: (1) dispersing a radically polymerizable monomer in a molten lactam In the monomer, a radical initiator is added to carry out radical polymerization of the radical polymerizable monomer to obtain a mixture of the radical polymer and the lactam monomer; or ( ⁇ ) to provide a radical polymer and a molten lactam single a mixture of bodies.
- a mixture of a free radical polymer and a lactam monomer can be prepared in situ (for example, step (1) can also be formed by mixing an existing free radical polymer with a molten lactam monomer (for example, step ( ) .
- the nylon microspheres are prepared in a continuous manner, wherein a mixture of the free radical polymer and the lactam monomer is first obtained by free radical polymerization as shown in step (1), and then the steps are carried out.
- the radical polymerization in the step (1) is preferably carried out at a temperature of from 60 to 150 °C.
- the polymerization time is usually from 4 to 72 hours, depending on the type and amount of the radical monomer.
- the solvent used for dissolving and removing the radical polymer in the step (3) is a solvent capable of dissolving the radical polymer but not dissolving the nylon, such as but not limited to: acetone, tetrahydrofuran (THF), Water, toluene, xylene, methyl ethyl ketone, ethyl acetate, propionitrile or a mixed solvent thereof.
- acetone tetrahydrofuran
- Water toluene
- xylene methyl ethyl ketone
- ethyl acetate ethyl acetate
- propionitrile or a mixed solvent thereof.
- One skilled in the art can readily select a suitable solvent for dissolving and removing the free radical polymer to obtain nylon microspheres.
- the method of the invention has the following main advantages:
- the production process is simple and easy to operate, and the energy consumption and production cost are low;
- Some of the reagents used can be recycled, for example, a solvent for dissolving and removing the radical polymer can be recycled, and the dissolved radical polymer can also be recycled;
- the particle diameter of the nylon microsphere can be effectively controlled within the range of 0.1 to 500 ⁇ m.
- effective control of the molecular weight of the nylon microspheres can be achieved, for example, the molecular weight can be controlled in the range of 10,000 to 300,000, preferably, the weight average molecular weight of the nylon is in the range of 10,000 to 80,000, and the particle diameter of the nylon microspheres is In the range of 0.5-100 microns. More preferably, the weight average molecular weight of the nylon is in the range of 25,000 to 60,000, and the particle diameter of the nylon microsphere is in the range of 1 to 50 ⁇ m.
- nylon microspheres having a regular spherical shape can be obtained. More preferably, the particle size and molecular weight of the resulting nylon microspheres can be controlled by adjusting the content of the free radical polymer.
- the nylon microspheres of the present invention can be used as a powder coating, a rotational molding, an extrusion molding raw material, and the like.
- Methyl methacrylate ( ⁇ ) (25% by weight;) was mixed with molten caprolactam, stirred at 80 ° C with constant temperature, and 0.2% by weight of azobisisobutyronitrile (AIBN;) was added for radical polymerization for 24 hours.
- AIBN azobisisobutyronitrile
- the mixture system was warmed to 160-180 ° C and evacuated for 20 minutes to remove residual MMA monomer and water.
- 4% by weight of sodium caprolactam and 0.4% by weight of 2,4-toluene diisocyanate (TDI) were added, mixed uniformly, and statically cast, and the mold temperature was controlled at 160-180 °C.
- the obtained polymethyl methacrylate (PMMA) / monomer cast nylon 6 (MCPA6) polymer alloy was coarsely pulverized, and then ruthenium was dissolved in acetone, and dried by filtration to obtain a desired nylon 6 microsphere.
- the molecular weight of the obtained nylon 6 microsphere gel chromatography (GPC) method was measured, and the volume average particle diameter was measured by a laser diffraction method.
- the results are shown in Table 1.
- a scanning electron microscope (SEM) photograph of the nylon 6 microspheres prepared in this example is shown in FIG. As can be seen from Fig. 1, spherical nylon particles having a regular shape can be obtained by the method of the present invention.
- Example 2 A scanning electron microscope (SEM) photograph of the nylon 6 microspheres prepared in this example is shown in FIG. As can be seen from Fig. 1, spherical nylon particles having a regular shape can be obtained by the method of the present invention.
- Methyl methacrylate (MMA) (20% by weight;) was mixed with molten octanolacide, stirred at 100 ° C with constant temperature, and 0.3% by weight of cumene hydroperoxide was added thereto, and radical polymerization was carried out for 20 hours.
- the mixture system was maintained at 120-140 ° C and evacuated for 20 minutes to remove residual MMA monomer and water. 4% by weight of sodium caprolactam and 0.4% by weight of TDI were added, mixed uniformly, and statically cast, and the mold temperature was controlled at 120-160 °C.
- the resulting polymethyl methacrylate (PMMA) / monomer cast nylon 8 (MCPA8) polymer alloy was coarsely crushed, then dissolved in acetone and filtered to dryness to obtain the desired nylon 8 microspheres.
- the obtained nylon 8 microspheres were measured for molecular weight by a gel chromatography (GPC) method, and their volume average particle diameters were measured by a laser diffraction method. The results are shown in Table 1.
- GPC gel chromatography
- the system was warmed to 130-150 ° C and evacuated for 20 minutes to remove residual styrene monomer and water.
- PS polystyrene
- MCPA6 / 8 monomer cast nylon 6 / 8
- the obtained polymer alloy was dissolved in tetrahydrofuran (THF) to remove PS, and dried by filtration to obtain the desired nylon 6/8 microspheres.
- the obtained nylon 6/8 microspheres were measured for molecular weight by a gel chromatography (GPC) method, and their volume average particle diameters were measured by a laser diffraction method. The results are shown in Table 1.
- GPC gel chromatography
- Styrene (10% by weight;) was mixed with molten caprolactam, stirred at a constant temperature of 60 ° C, and 0.2 wt% of AIBN was added to initiate styrene radical polymerization, and polymerization was carried out for 24 hours.
- the system was heated to 100-140 ° C and evacuated for 20 minutes to remove residual styrene monomer and water. Add 4 weights / ( ⁇ 11, 0.4 weight ° / ( ⁇ 01, evenly mixed, static casting, mold temperature control at 160 ⁇ 180 ° C.
- Vinylpyrrolidone (10% by weight;) was mixed with molten butyrolactam, stirred at 80 ° C with constant temperature, and 0.3% by weight of AIBN was added to initiate radical polymerization, and radical polymerization was carried out for 24 hours.
- the temperature of the system was raised to about 180 ° C and evacuated for 30 minutes to remove residual vinylpyrrolidone monomer and water.
- the resulting polyvinylpyrrolidone (; PVP) / monomer cast nylon 4 (MCPA4) polymer alloy was coarsely crushed, then PVP was dissolved in water, and dried by filtration to obtain the desired nylon 4 microspheres.
- the obtained nylon 4 microspheres were measured for molecular weight by a gel chromatography (GPC) method, and their volume average particle diameters were measured by a laser diffraction method. The results are shown in Table 1.
- PVP polyvinylpyrrolidone
- MCPA4 monomer cast nylon 4
- Methylstyrene (50% by weight;) was mixed with molten decanolacide, stirred at 100 ° C with constant temperature, and 0.3% by weight of AIBN was added to initiate methyl styrene radical polymerization, and polymerization was carried out for 24 hours.
- the temperature of the system was maintained at 160-170 ° C and evacuated for 30 minutes to remove residual methyl styrene monomer and water.
- the resulting polymethylstyrene (PMS)/monomer cast nylon 10 (MCPA10) polymer alloy was coarsely crushed, then PMS was dissolved in toluene, and dried by filtration to obtain the desired nylon 10 microspheres.
- the obtained nylon 10 microspheres were measured for molecular weight by a gel chromatography (GPC) method, and their volume average particle diameters were measured by a laser diffraction method. The results are shown in Table 1.
- GPC gel chromatography
- the temperature of the system was maintained at 150 ° C - 170 ° C and evacuated for 20 minutes to remove residual acrylonitrile monomer and water. Add 2% by weight of sodium caprolactam, 0.2 weight ° / ⁇ ⁇ 01, mix evenly, static casting, The mold temperature is controlled at 160-190 °C.
- the resulting polyacrylonitrile (PAN) / monomer cast nylon 12 (MCPA12) polymer alloy was coarsely crushed, then PAN was dissolved in propionitrile and filtered to dryness to obtain the desired nylon 12 microspheres.
- the obtained nylon 12 microspheres were measured for molecular weight by a gel chromatography (GPC) method, and their volume average particle diameters were measured by a laser diffraction method. The results are shown in Table 1.
- GPC gel chromatography
- Polystyrene (PS) PS of Model 666D purchased from Yanshan Petrochemical Co., Ltd., having a molecular weight of 260,000 X 15% by weight;
- molten caprolactam were mixed and stirred at 120 ° C with constant temperature.
- the mixture system was heated to 160-180 ° C, 4% by weight of sodium caprolactam, 0.4% by weight of 2,4-toluene diisocyanate (TDI) was added, uniformly mixed, and statically cast, and the mold temperature was controlled at 160-180 °C.
- TDI 2,4-toluene diisocyanate
- the obtained polystyrene (PS) / monomer cast nylon 6 (MCPA6) polymer alloy was coarsely pulverized, and then PS was dissolved in toluene, and dried by filtration to obtain a desired nylon 6 microsphere.
- the obtained nylon 6 microspheres were measured for molecular weight by a gel chromatography (GPC) method, and their volume average particle diameters were measured by a laser diffraction method. The results are shown in Table 1.
- GPC gel chromatography
- Methyl methacrylate (15% by weight;) and molten caprolactam were mixed, stirred at 90 ° C with constant temperature, and 0.4% by weight of dibenzoyl peroxide (BPO) was added to initiate radical polymerization, and the reaction was carried out for 24 hours.
- BPO dibenzoyl peroxide
- the system was warmed to 150-180 ° C and evacuated for 20 minutes to remove residual monomer and water.
- the above system was introduced into a reaction extruder, and 4% by weight of sodium caprolactam was added, and 0.4 weight/( ⁇ 01) was subjected to reaction extrusion, and the temperature was controlled at 250 °C.
- the obtained polymer alloy of polymethyl methacrylate (PMM A) / nylon 6 (P A6) was dissolved in acetone to dissolve PMMA, and dried to obtain a desired nylon 6 microsphere.
- the obtained nylon 6 microspheres were measured for molecular weight by a gel permeation chromatography (GPC) method, and their volume average particle diameters were measured by a laser diffraction method. The results are shown in Table 1.
- GPC gel permeation chromatography
- Styrene (40% by weight;) and molten caprolactam were mixed, stirred at 80 ° C under constant temperature, and 0.3% by weight of AIBN was added to initiate styrene radical polymerization, and polymerization was carried out for 24 hours.
- the system was warmed to 100-120 ° C and evacuated for 20 minutes to remove residual styrene monomer and water.
- the above system was introduced into a reaction extruder, and 2% by weight of sodium caprolactam and 0.2% by weight of butyl 01 were added for reaction extrusion, and the reaction temperature was controlled at 250 °C.
- the obtained polymer alloy of polystyrene (PS) / nylon 6 (PA6) was dissolved in THF with THF and dried to obtain the desired nylon 6 microspheres.
- the obtained nylon 6 microspheres were measured for molecular weight by a gel chromatography (GPC) method, and their volume average particle diameters were measured by a laser diffraction method. The results are shown in Table 1.
- GPC gel chromatography
- Vinylpyrrolidone (25% by weight;) and molten caprolactam were mixed, stirred at 90 ° C under constant temperature, and 0.3% by weight of 8?0 was added to initiate radical polymerization, and polymerization was carried out for 24 hours.
- the system was warmed to 120-140 ° C and evacuated for 20 minutes to remove residual vinylpyrrolidone monomer and water.
- the above system was introduced into a reaction extruder, and 2% by weight of sodium caprolactam and 0.2% by weight of acetyl chloride were added to carry out reactive extrusion, and the reaction temperature was controlled at 230 °C.
- polyvinylpyrrolidone (PVP)/nylon 6 (PA6) polymer alloy was dissolved in water with PVP and filtered to dryness to obtain the desired nylon 6 microspheres.
- the obtained nylon 6 microspheres were measured for molecular weight by a gel chromatography (GPC) method, and their volume average particle diameters were measured by a laser diffraction method. The results are shown in Table 1.
- GPC gel chromatography
- Vinylpyrrolidone (40% by weight;) and molten octanolacide were mixed, stirred at 120 ° C with constant temperature, and 0.3% by weight of cumene hydroperoxide was added to carry out radical polymerization for 24 hours.
- the system was heated to 120 ° C to 180 ° C and evacuated for 20 minutes to remove residual vinylpyrrolidone monomer and water.
- the above system was introduced into a reaction extruder, and 2% by weight of sodium carbonate and 0.2% by weight of butyl 01 were added to carry out reactive extrusion, and the reaction temperature was controlled at 250 °C.
- polyvinylpyrrolidone (PVP)/nylon 8 (PA8) polymer alloy was dissolved in water with PVP and filtered to dryness to obtain the desired nylon 8 microspheres.
- the obtained nylon 8 microspheres were measured for molecular weight by a gel chromatography (GPC) method, and their volume average particle diameters were measured by a laser diffraction method. The results are shown in Table 1.
- GPC gel chromatography
- the system was heated to 150 ° C to 180 ° C and evacuated for 20 minutes to leave monomer and water.
- the above system was introduced into a reaction extruder, and 2% by weight of sodium caprolactam and 0.2% by weight of butyl 01 were added to carry out reactive extrusion, and the reaction temperature was controlled at 250 °C.
- the resulting polyacrylamide (P AM)/nylon 12 (PA12) polymer alloy dissolved PVP in water and was filtered to dryness to give the desired nylon 12 microspheres.
- the obtained nylon 12 microspheres were measured for molecular weight by a gel chromatography (GPC) method, and their volume average particle diameters were measured by a laser diffraction method. The results are shown in Table 1.
- GPC gel chromatography
- PMMAX Polymethyl methacrylate (PMMAX was purchased from Shanghai Pen Chemical Co., Ltd., model 255, molecular weight of 122,000) (20% by weight;) and molten caprolactam were mixed and stirred at 80 ° C with constant temperature.
- the mixture system was heated to 160-180 ° C, and 4% by weight of sodium caprolactam and 0.4% by weight of TDI were added to carry out reactive extrusion, and the reaction temperature was controlled at 250 °C.
- the obtained polymer alloy of polymethyl methacrylate (PMMA) / nylon 6 (PA6) was coarsely pulverized, and then PMMA was dissolved in acetone, and dried by filtration to obtain a desired nylon 6 microsphere.
- the obtained nylon 6 microspheres were measured for molecular weight by a gel chromatography (GPC) method, and the volume average particle diameter was measured by a laser diffraction method. The results are shown in Table 1.
- GPC gel chromatography
- the obtained polymer alloy was coarsely crushed, the styrene-methylstyrene copolymer was dissolved in water, and dried by filtration to obtain a desired nylon 6 microsphere.
- the obtained nylon 6 microspheres were measured for molecular weight by a gel chromatography (GPC) method, and their volume average particle diameters were measured by a laser diffraction method. The results are shown in Table 1.
- Example 16 Styrene (5 wt%;) and molten caprolactam were mixed, stirred at 100 ° C under constant temperature, and 0.04 wt% AIBN was added to initiate radical polymerization to obtain a polystyrene/caprolactam solution, and 0.2 wt% was added to the mixed solution.
- / ⁇ 011 and 2% by weight of 1101 (hexamethylene diisocyanate) were then polymerized in a mold, and the reaction temperature was controlled at 240 °C.
- the obtained polymer alloy was coarsely crushed, polystyrene was dissolved in water, and dried by filtration to obtain a desired nylon 6 microsphere.
- the obtained nylon 6 microspheres were measured for molecular weight by a gel chromatography (GPC) method, and their volume average particle diameters were measured by a laser diffraction method. The results are shown in Table 1.
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BRPI0711874-0A BRPI0711874B1 (pt) | 2006-05-23 | 2007-05-22 | Método para preparar microsferas de náilon |
EP07721661.2A EP2022809B1 (en) | 2006-05-23 | 2007-05-22 | A method for preparing nylon microsphere and the same |
KR1020087030159A KR101408574B1 (ko) | 2006-05-23 | 2007-05-22 | 나일론 마이크로스피어 제조방법 및 이 방법에 의해 제조된 나일론 마이크로스피어 |
AU2007252124A AU2007252124B2 (en) | 2006-05-23 | 2007-05-22 | A method for preparing nylon microsphere and the same |
JP2009511325A JP5059104B2 (ja) | 2006-05-23 | 2007-05-22 | ナイロンマイクロボールの製造方法およびマイクロボール |
CA2652997A CA2652997C (en) | 2006-05-23 | 2007-05-22 | Method for preparing nylon microspheres and nylon microspheres prepared thereby |
US12/269,428 US8048967B2 (en) | 2006-05-23 | 2008-11-12 | Method for preparing nylon microspheres and nylon microspheres prepared thereby |
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CN2006100268059A CN101077910B (zh) | 2006-05-23 | 2006-05-23 | 一种制备粒径可控的高分子量尼龙微球的方法 |
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EP (1) | EP2022809B1 (zh) |
JP (1) | JP5059104B2 (zh) |
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CN101768282B (zh) * | 2008-12-29 | 2012-05-30 | 合肥杰事杰新材料股份有限公司 | 一种熔点及粒径可控的尼龙无规共聚物微球的制备方法 |
CN102115536B (zh) * | 2009-12-30 | 2012-12-26 | 合肥杰事杰新材料股份有限公司 | 一种聚酰胺/苯乙烯梳状接枝聚合物的制备方法 |
KR20130118291A (ko) | 2010-06-23 | 2013-10-29 | 나가세케무텍쿠스가부시키가이샤 | 내충격성 폴리아미드 조성물 및 그 제조 방법 |
CN102477220B (zh) * | 2010-11-23 | 2014-06-25 | 合肥杰事杰新材料股份有限公司 | 一种粒径可控的磁性尼龙微球及其制备方法 |
CN103665839B (zh) * | 2012-09-14 | 2017-02-08 | 合肥杰事杰新材料股份有限公司 | 一种聚酰胺微球及其制备方法 |
CN104059235A (zh) * | 2013-03-19 | 2014-09-24 | 上海杰事杰新材料(集团)股份有限公司 | 一种紫外吸收型尼龙微球及其制备方法 |
CN104558588B (zh) * | 2013-10-22 | 2017-09-29 | 中国石油化工股份有限公司 | 一种尼龙聚合物及其制备方法 |
CN104045826B (zh) * | 2014-06-25 | 2016-03-30 | 江苏科技大学 | 一种聚酰胺微球的环保型制备方法 |
CN104630925B (zh) * | 2015-02-05 | 2017-04-05 | 江苏科技大学 | 一种聚酰胺微纳米纤维的反应挤出制备方法 |
CN107973878B (zh) * | 2016-10-25 | 2020-06-09 | 中国石油化工股份有限公司 | 一种共聚物及其制备方法和应用以及共混材料 |
CN107936550A (zh) * | 2017-11-29 | 2018-04-20 | 华东理工大学 | 一种聚苯乙烯/尼龙6复合材料及其制备方法 |
CN108752579B (zh) * | 2018-06-13 | 2020-10-20 | 青岛罗泰克亿利汽车橡塑制品有限公司 | 液态尼龙配方及滚塑成型工艺 |
CN111969191B (zh) * | 2020-08-26 | 2021-12-10 | 山东兴丰新能源科技有限公司 | 基于金属氧化物的锂离子电池负极材料及其制备方法 |
CN114621485B (zh) * | 2022-04-12 | 2023-04-07 | 滨州学院 | 树莓状多孔聚酰胺微球制备方法及制备的聚酰胺材料 |
CN114752029B (zh) * | 2022-05-18 | 2023-07-21 | 江苏科技大学 | 尼龙6柔性热敏感微球及其制备方法和应用 |
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- 2007-05-22 KR KR1020087030159A patent/KR101408574B1/ko active IP Right Grant
- 2007-05-22 EP EP07721661.2A patent/EP2022809B1/en active Active
- 2007-05-22 RU RU2008150861/04A patent/RU2411257C2/ru active
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US8048967B2 (en) | 2011-11-01 |
US20090123753A1 (en) | 2009-05-14 |
RU2008150861A (ru) | 2010-06-27 |
JP2009537672A (ja) | 2009-10-29 |
BRPI0711874A2 (pt) | 2012-01-10 |
EP2022809A1 (en) | 2009-02-11 |
BRPI0711874B1 (pt) | 2018-05-29 |
CN101077910A (zh) | 2007-11-28 |
EP2022809B1 (en) | 2016-03-23 |
CA2652997A1 (en) | 2007-11-29 |
AU2007252124A1 (en) | 2007-11-29 |
JP5059104B2 (ja) | 2012-10-24 |
EP2022809A4 (en) | 2010-07-28 |
CN101077910B (zh) | 2010-06-09 |
RU2411257C2 (ru) | 2011-02-10 |
AU2007252124B2 (en) | 2010-07-01 |
KR101408574B1 (ko) | 2014-07-02 |
CA2652997C (en) | 2012-09-18 |
KR20090083277A (ko) | 2009-08-03 |
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