Classifications

• • H—ELECTRICITY
  • H01—ELECTRIC ELEMENTS
  • H01F—MAGNETS; INDUCTANCES; TRANSFORMERS; SELECTION OF MATERIALS FOR THEIR MAGNETIC PROPERTIES
  • H01F1/00—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties
  • H01F1/01—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials
  • H01F1/03—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity
  • H01F1/032—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of hard-magnetic materials
  • H01F1/04—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of hard-magnetic materials metals or alloys
  • H01F1/047—Alloys characterised by their composition
  • H01F1/053—Alloys characterised by their composition containing rare earth metals
  • H01F1/055—Alloys characterised by their composition containing rare earth metals and magnetic transition metals, e.g. SmCo5
  • H01F1/0551—Alloys characterised by their composition containing rare earth metals and magnetic transition metals, e.g. SmCo5 in the form of particles, e.g. rapid quenched powders or ribbon flakes
  • H01F1/0552—Alloys characterised by their composition containing rare earth metals and magnetic transition metals, e.g. SmCo5 in the form of particles, e.g. rapid quenched powders or ribbon flakes with a protective layer
• • H—ELECTRICITY
  • H01—ELECTRIC ELEMENTS
  • H01F—MAGNETS; INDUCTANCES; TRANSFORMERS; SELECTION OF MATERIALS FOR THEIR MAGNETIC PROPERTIES
  • H01F1/00—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties
  • H01F1/01—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials
  • H01F1/03—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity
  • H01F1/032—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of hard-magnetic materials
  • H01F1/04—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of hard-magnetic materials metals or alloys
  • H01F1/047—Alloys characterised by their composition
  • H01F1/053—Alloys characterised by their composition containing rare earth metals
  • H01F1/055—Alloys characterised by their composition containing rare earth metals and magnetic transition metals, e.g. SmCo5
  • H01F1/0555—Alloys characterised by their composition containing rare earth metals and magnetic transition metals, e.g. SmCo5 pressed, sintered or bonded together
  • H01F1/0558—Alloys characterised by their composition containing rare earth metals and magnetic transition metals, e.g. SmCo5 pressed, sintered or bonded together bonded together
• • H—ELECTRICITY
  • H01—ELECTRIC ELEMENTS
  • H01F—MAGNETS; INDUCTANCES; TRANSFORMERS; SELECTION OF MATERIALS FOR THEIR MAGNETIC PROPERTIES
  • H01F1/00—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties
  • H01F1/01—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials
  • H01F1/03—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity
  • H01F1/032—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of hard-magnetic materials
  • H01F1/04—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of hard-magnetic materials metals or alloys
  • H01F1/047—Alloys characterised by their composition
  • H01F1/053—Alloys characterised by their composition containing rare earth metals
  • H01F1/055—Alloys characterised by their composition containing rare earth metals and magnetic transition metals, e.g. SmCo5
  • H01F1/057—Alloys characterised by their composition containing rare earth metals and magnetic transition metals, e.g. SmCo5 and IIIa elements, e.g. Nd2Fe14B
  • H01F1/0571—Alloys characterised by their composition containing rare earth metals and magnetic transition metals, e.g. SmCo5 and IIIa elements, e.g. Nd2Fe14B in the form of particles, e.g. rapid quenched powders or ribbon flakes
  • H01F1/0572—Alloys characterised by their composition containing rare earth metals and magnetic transition metals, e.g. SmCo5 and IIIa elements, e.g. Nd2Fe14B in the form of particles, e.g. rapid quenched powders or ribbon flakes with a protective layer
• • H—ELECTRICITY
  • H01—ELECTRIC ELEMENTS
  • H01F—MAGNETS; INDUCTANCES; TRANSFORMERS; SELECTION OF MATERIALS FOR THEIR MAGNETIC PROPERTIES
  • H01F1/00—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties
  • H01F1/01—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials
  • H01F1/03—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity
  • H01F1/032—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of hard-magnetic materials
  • H01F1/04—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of hard-magnetic materials metals or alloys
  • H01F1/047—Alloys characterised by their composition
  • H01F1/053—Alloys characterised by their composition containing rare earth metals
  • H01F1/055—Alloys characterised by their composition containing rare earth metals and magnetic transition metals, e.g. SmCo5
  • H01F1/057—Alloys characterised by their composition containing rare earth metals and magnetic transition metals, e.g. SmCo5 and IIIa elements, e.g. Nd2Fe14B
  • H01F1/0571—Alloys characterised by their composition containing rare earth metals and magnetic transition metals, e.g. SmCo5 and IIIa elements, e.g. Nd2Fe14B in the form of particles, e.g. rapid quenched powders or ribbon flakes
  • H01F1/0575—Alloys characterised by their composition containing rare earth metals and magnetic transition metals, e.g. SmCo5 and IIIa elements, e.g. Nd2Fe14B in the form of particles, e.g. rapid quenched powders or ribbon flakes pressed, sintered or bonded together
  • H01F1/0578—Alloys characterised by their composition containing rare earth metals and magnetic transition metals, e.g. SmCo5 and IIIa elements, e.g. Nd2Fe14B in the form of particles, e.g. rapid quenched powders or ribbon flakes pressed, sintered or bonded together bonded together
• • H—ELECTRICITY
  • H01—ELECTRIC ELEMENTS
  • H01F—MAGNETS; INDUCTANCES; TRANSFORMERS; SELECTION OF MATERIALS FOR THEIR MAGNETIC PROPERTIES
  • H01F1/00—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties
  • H01F1/01—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials
  • H01F1/03—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity
  • H01F1/032—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of hard-magnetic materials
  • H01F1/04—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of hard-magnetic materials metals or alloys
  • H01F1/047—Alloys characterised by their composition
  • H01F1/053—Alloys characterised by their composition containing rare earth metals
  • H01F1/055—Alloys characterised by their composition containing rare earth metals and magnetic transition metals, e.g. SmCo5
  • H01F1/059—Alloys characterised by their composition containing rare earth metals and magnetic transition metals, e.g. SmCo5 and Va elements, e.g. Sm2Fe17N2
• • H—ELECTRICITY
  • H01—ELECTRIC ELEMENTS
  • H01F—MAGNETS; INDUCTANCES; TRANSFORMERS; SELECTION OF MATERIALS FOR THEIR MAGNETIC PROPERTIES
  • H01F41/00—Apparatus or processes specially adapted for manufacturing or assembling magnets, inductances or transformers; Apparatus or processes specially adapted for manufacturing materials characterised by their magnetic properties
  • H01F41/02—Apparatus or processes specially adapted for manufacturing or assembling magnets, inductances or transformers; Apparatus or processes specially adapted for manufacturing materials characterised by their magnetic properties for manufacturing cores, coils, or magnets
  • H01F41/0253—Apparatus or processes specially adapted for manufacturing or assembling magnets, inductances or transformers; Apparatus or processes specially adapted for manufacturing materials characterised by their magnetic properties for manufacturing cores, coils, or magnets for manufacturing permanent magnets
  • H01F41/0266—Moulding; Pressing

Definitions

• the present disclosure relates to the field of rare earth permanent magnets, in particular to a surface treatment method of rare earth magnetic powder, an injection molding rare earth magnetic material and a preparation method thereof.
• An injection molding magnet is made by melting, blending, extruding and granulating organic polymer resin and magnetic powder.
• Commonly used polymer resins include polyamide PA6, PA66, PA12, PA11, and PA612 series and polyphenylene sulfide (PPS) with the better temperature resistance, polyether ether ketone (PEEK) and the like;
• the magnetic powder include a lower-performance ferrite (FeO) and higher-performance rare earths magnetic powder: neodymium iron boron (Nd-Fe-B), samarium iron nitrogen (Sm-Fe-N), samarium cobalt (Sm-Co) and the like.
• the rare earth magnetic powder is different from ferrite powder, and the rare earth magnetic powder itself belongs to alloy powder. In a granulation process, due to the higher temperature required, the magnetic powder is extremely easy to be oxidized, so that the performance thereof is significantly reduced, especially the rare earth powder with the finer powder particle size, such as anisotropic SmFeN powder.
• the surface treatment on the rare earth magnetic powder it is usually necessary to firstly perform the surface treatment on the rare earth magnetic powder to provide a protective layer on the surface of the magnetic powder, so that the oxidation of the magnetic powder may be reduced in a treatment process, and the magnetic performance thereof is protected.
• many companies use a mode of coupling-treatment to treat the surface of magnetic powder, and the coupling-treatment mode may improve the bondability with binders PA and PPS.
• the binder After the binder is dissolved in a double-screw extruder, it wraps the magnetic powder, the magnetic powder inside the binder may be protected from being oxidized, but before the binder completely wraps the magnetic powder, the magnetic powder may still be oxidized to a large extent.
• a patent CN201510454107.8 also mentions a method of treating rare earth SmFeN magnetic powder by immersing the magnetic powder in coupling agent and phosphoric acid composite solution.
• phosphoric acid solution Through phosphoric acid solution, a certain phosphating film may be formed on the surface of the powder, thereby the high temperature resistance of the magnetic powder is improved, and the magnetic powder is protected from being oxidized during a granulation process.
• a phosphoric acid forms a phosphate crystal nucleus on an active site of the surface of the magnetic powder, and then the crystal nucleus continues to grow, to form the stable phosphating film.
• the quality and integrity of the phosphating film are greatly related to the number of the active points on the surface of the magnetic powder.
• the active site on the surface of the magnetic powder is very weak, and it is difficult to form the stable and high-quality phosphating film, so that in the subsequent high-temperature granulation process, the rare earth magnetic powder after the treatment still has a risk of being oxidized to a large extent.
• a main purpose of the present disclosure is to provide a surface treatment method of rare earth magnetic powder, an injection molding rare earth magnetic material and a preparation method thereof, as to solve a problem in an existing technology that that the rare earth magnetic powder has weak oxidation resistance, so that the rare earth magnetic material after injection molding is poor in magnetic performance.
• a surface treatment method of rare earth magnetic powder includes the following steps: step S1, adding rare earth magnetic powder to weak acid solution, as to weakly acidify the surface of the rare earth magnetic powder, to form weakly acidified magnetic powder, herein a weak acid in the weak acid solution is an inorganic weak acid with an acidity coefficient pKa value greater than 4.5 and/or an organic weak acid with an acidity coefficient greater than 1.0; step S2, phosphating the weakly acidified magnetic powder with phosphating solution, to form phosphating magnetic powder; and step S3, mixing the phosphating magnetic powder with a coupling agent, as to coupling-treat the phosphating magnetic powder, and then drying, to obtain a surface treated rare earth magnetic powder.
• the weak acid is one or more of an oxalic acid, an acetic acid and a carbonic acid; preferably, a pH value of the weak acid solution is 5-7; preferably, ethanol is used to adjust the pH value of the weak acid solution; and preferably, a volume ratio of the weak acid solution to the rare earth magnetic powder is 1.5-3:1.
• step S1 after adding the rare earth magnetic powder to the weak acid solution, performing a first ultrasonic vibration, as to perform the weak acidification treatment; preferably, the power of the first ultrasonic vibration is 1500-2500 W, and the time length is 2-5 min.
• the phosphating solution is zinc-based phosphating solution or manganese-based phosphating solution; preferably, after the weak acidification treatment is completed, the phosphating solution is directly added to a system containing the weakly acidified magnetic powder, until a pH value of the system reaches 4-5, and then a second ultrasonic vibration is performed, as to perform the phosphating treatment; and preferably, the power of the second ultrasonic vibration is 1000-1500 W, and the time length is 10-15 min.
• the coupling agent is a silane coupling agent, preferably one or more of KH550, KH560, and KH792; preferably, after the phosphating treatment is completed, the coupling agent is directly added to a system containing the phosphating magnetic powder, and then a third ultrasonic vibration is performed, as to perform the coupling treatment; preferably, the added amount of the coupling agent is 0.5-1 % of the weight of the rare earth magnetic powder; preferably, the power of the third ultrasonic vibration is 1200-2000 W, and the time length is 10-15 min; and preferably, the drying process adopts vacuum drying, and the drying temperature is 70-90°C.
• the rare earth magnetic powder is one or more of isotropic neodymium iron boron magnetic powder, anisotropic neodymium iron boron magnetic powder, isotropic samarium iron nitrogen magnetic powder, anisotropic samarium iron nitrogen magnetic powder and samarium cobalt magnetic powder.
• a preparation method for an injection molding rare earth magnetic material includes the following steps: using the above surface treatment method to perform surface treatment on rare earth magnetic powder; and mixing the surface treated rare earth magnetic powder with a binder, and then extruding and granulating, to obtain the injection molding rare earth magnetic material.
• the binder is one or more of nylon, polyphenylene sulfide, and polyether ether ketone; preferably, the amount of the binder is 8-15% of the weight of the rare earth magnetic powder.
• the extruding and granulating process adopts a double-screw extruder, and the temperature of the extruding and granulating is 200-310°C.
• an injection molding rare earth magnetic material is further provided, and it is prepared by the above preparation method.
• the present disclosure provides a surface treatment method of rare earth magnetic powder, and it is to sequentially perform the weak acidification treatment, the phosphating treatment and the coupling treatment on the rare earth magnetic powder.
• the weak acidification treatment is the basis of the phosphating treatment and the coupling treatment, it may increase the number of the active sites on the surface of the rare earth magnetic powder, and may also dissolve insoluble ferrous iron and iron compound impurities on the surface of the rare earth magnetic powder, so that it is converted into a weak acid ferrous iron.
• the phosphating treatment and the coupling treatment are performed after the weak acidification treatment, and the more complete and higher-quality phosphating film and coupling protective layer may be formed on the surface of the rare earth magnetic powder, thereby the treated rare earth magnetic powder has the better oxidation resistance, the rare earth magnetic powder may be protected and prevented from being oxidized before and during the subsequent injection molding with the binder, and the obtained injection molding rare earth magnetic material has the better magnetic performance correspondingly.
• the rare earth magnetic powder in the existing technology has the weak oxidation resistance, so that the rare earth magnetic material after injection molding is poor in magnetic performance.
• the present disclosure provides a surface treatment method of rare earth magnetic powder, and it includes the following steps:
• the present disclosure provides a surface treatment method of rare earth magnetic powder, and it is to sequentially perform the weak acidification treatment, the phosphating treatment and the coupling treatment on the rare earth magnetic powder.
• the weak acidification treatment is the basis of the phosphating treatment and the coupling treatment, it may increase the number of the active sites on the surface of the rare earth magnetic powder, and may also dissolve insoluble ferrous iron and iron compound impurities on the surface of the rare earth magnetic powder, so that it is converted into a weak acid ferrous iron.
• the increase in the number of the active sites may increase the number of sites on the surface of the rare earth magnetic powder that participate in a phosphating reaction and a coupling reaction, so that the degree of phosphating during the phosphating treatment may be improved, and the coupling treatment is also more adequate.
• the weak acid ferrous iron formed by the dissolution of impurities such as ferrous iron and iron compounds close to or remaining on the surface of the rare earth magnetic powder may act as a phosphating nucleus to a certain extent during the phosphating process, and it is also beneficial to the growth and formation of the phosphating film.
• the above two reasons are both helpful to improve the integrity and quality of the phosphating film, and the coupling protective layer is also more complete correspondingly.
• the phosphating treatment and the coupling treatment are performed after the weak acidification treatment, and the more complete and higher-quality phosphating film and coupling protective layer may be formed on the surface of the rare earth magnetic powder, thereby the treated rare earth magnetic powder has the better oxidation resistance, the rare earth magnetic powder may be protected and prevented from being oxidized before and during the subsequent injection molding with the binder, and the obtained injection molding rare earth magnetic material has the better magnetic performance correspondingly.
• the present disclosure sequentially performs the phosphating treatment and the coupling treatment after the weak acidification treatment, so that the growth of the phosphating film is more complete, and correspondingly the coupling protective layer is also more complete, it is further beneficial to the improvement of the oxidation resistance of the rare earth magnetic powder.
• this operation is more beneficial to improve the compatibility and binding force of the rare earth magnetic powder with a polymer material during a later mixing and granulating process of the rare earth magnetic powder.
• the surface treatment method provided by the present disclosure is used to treat the rare earth magnetic powder, it may significantly improve the oxidation resistance thereof, and correspondingly it is possible to prepare the high-performance and high-stability injection molding rare earth magnetic material.
• the above weak acid adopts an inorganic weak acid with an acidity coefficient pKa value greater than 4.5 and/or an organic weak acid with an acidity coefficient greater than 1.0, it may increase the number of the active sites on the surface of the magnetic powder as much as possible on the basis without harming a body of the rare earth magnetic powder, in order to make the weak acidification treatment more effective, in a preferred embodiment, the weak acid adopts one or more of an oxalic acid, an acetic acid and a carbonic acid.
• a pH of the weak acid solution is 5-7.
• the pH value of the weak acid solution is controlled within the above range, it is beneficial to control the stability of the weak acidification treatment, and at the same time promotes the weak acidification treatment to be more adequate, so it has the further promotion effect on the growth quality and integrity of the subsequent phosphating film and coupling protective layer.
• ethanol may be used as a pH adjuster to adjust the pH value of the weak acid solution to 5-7.
• a specific solvent in the weak acid solution includes, but is not limited to, one or more of isopropanol, ethanol, and deionized water.
• the added amount of the above weak acid solution should be sufficient to wrap the rare earth magnetic powder.
• the volume ratio of the weak acid solution to the rare earth magnetic powder is 1.5-3:1.
• the weak acidification treatment may also dissolve the ferrous iron and iron compound impurities on the surface of the rare earth magnetic powder, and convert it into the weak acid ferrous iron.
• These weak acid ferrous irons play a role of the phosphating nucleus to a certain extent in the phosphating process.
• first ultrasonic vibration is performed, as to perform the weak acidification treatment. Through the ultrasonic vibration, the weak acid ferrous irons may be more evenly distributed on the surface of the weakly acidified magnetic powder, thereby the growth of the phosphating film is more uniform and complete, and it is also helpful to improve the efficiency of the phosphating treatment.
• the power of the first ultrasonic vibration is 1500-2500 W, and the time length is 2-5 min. Under this power and time length, the above effects may be fully exerted.
• the preferred power is 2000 W.
• the phosphating solution is zinc-based phosphating solution or manganese-based phosphating solution (available from Enthusiasm Company).
• the use of the above phosphating solution may perform more sufficient phosphating treatment on the weakly acidified magnetic powder, and the formed phosphating film is higher in quality, and is more complete and stable.
• the zinc-based phosphating solution is used as the phosphating solution (such as Enthusiasm BW-231 special material zinc-manganese-based phosphating solution).
• the phosphating solution is directly added to a system containing the weakly acidified magnetic powder, until a pH value of the system reaches 4-5, and then, second ultrasonic vibration is performed, as to perform the phosphating treatment.
• the second ultrasonic vibration treatment and the first ultrasonic vibration treatment are uninterrupted, so that the addition of the phosphating solution and the phosphating treatment may be performed under a condition of continuous vibration, and the effect is better.
• the power of the second ultrasonic vibration is 1000-1500 W, and the time length is 10-15 min, more preferably the power is 1500 W.
• the above coupling agent may adopt a commonly used type in the field, and preferably, the coupling agent is a silane coupling agent.
• the use of the silane coupling agent may form the better coupling protective film on the surface of the phosphating magnetic powder, and it may further improve the fusion between the magnetic powder and the binder during the subsequent injection molding granulating process with the binder, so that the material distribution is more uniform, and the magnetic performance of the final material is better.
• the coupling agent is one or more of KH550, KH560, and KH792.
• the coupling agent is directly added to a system containing the phosphating magnetic powder, and then third ultrasonic vibration is performed, as to perform the coupling treatment.
• the third ultrasonic vibration and the second ultrasonic vibration are uninterrupted, so that the coupling treatment may be performed under a state of continuous vibration, and the coupling protective layer formed is more uniform and complete.
• the added amount of the coupling agent is 0.5-1 % of the weight of the rare earth magnetic powder.
• the amount of the coupling agent is controlled within the above range, so that it may be fully distributed on the surface of the phosphating magnetic powder, it is more beneficial to improve the oxidation resistance of the magnetic powder and the compatibility between the magnetic powder and the binder during the injection molding process, so that the final material obtained by the granulation has the better magnetic performance and stability.
• the power of the third ultrasonic vibration is 1200-2000 W, and the time length is 10-15 min; and the preferred power is 1500 W.
• the drying process adopts vacuum drying, and the drying temperature is 70-90°C.
• the above surface treatment method of the present disclosure is suitable for many types of rare earth magnetic powder, including but not limited to the rare earth magnetic powder which is one or more of isotropic neodymium iron boron magnetic powder (Nd-Fe-B), anisotropic neodymium iron boron magnetic powder (Nd-Fe-B), isotropic samarium iron nitrogen magnetic powder (Sm-Fe-N), anisotropic samarium iron nitrogen magnetic powder (Sm-Fe-N) and samarium cobalt magnetic powder (Sm-Co).
• the rare earth magnetic powder which is one or more of isotropic neodymium iron boron magnetic powder (Nd-Fe-B), anisotropic neodymium iron boron magnetic powder (Nd-Fe-B), isotropic samarium iron nitrogen magnetic powder (Sm-Fe-N), anisotropic samarium iron nitrogen magnetic powder (Sm-Fe-N) and sam
• a preparation method for an injection molding rare earth magnetic material includes the following steps: using the above surface treatment method to perform surface treatment on rare earth magnetic powder; and mixing the surface treated rare earth magnetic powder with a binder, and then extruding and granulating, to obtain the injection molding rare earth magnetic material.
• the surface treatment method provided by the present disclosure is used to treat the rare earth magnetic powder, the oxidation resistance thereof may be significantly improved, and the rare earth magnetic powder may be protected and prevented from being oxidized before and during the subsequent injection molding with the binder, and correspondingly the high-performance high-stability injection molding rare earth magnetic material may be prepared.
• the above binder may be nylon, such as nylon 6, nylon 12, nylon 11, and nylon 66, or it may be polyphenylene sulfide (PPS) with the better temperature resistance, or polyether ether ketone (PEEK) and other materials. These materials may be used by one or a combination of them.
• PPS polyphenylene sulfide
• PEEK polyether ether ketone
• the amount of the binder is 8-15% of the weight of the rare earth magnetic powder.
• the extruding and granulating process adopts a double-screw extruder, and the temperature of the extruding and granulating is 200-310°C.
• an injection molding rare earth magnetic material is further provided, and it is prepared by the above preparation method.
• the injection molding rare earth magnetic material has the more excellent magnetic performance and stability.
• oxalic acid isopropanol solution 0.01 mol/L of oxalic acid isopropanol solution is dissolved in absolute ethanol, a pH value is adjusted to 5, to form weak acid solution; rare earth magnetic powder is added to it, the weak acid solution may completely wrap the magnetic powder, and its volume ratio to the magnetic powder is 1.5:1; ultrasonic vibration is turned on, the power is controlled to 2000 W, and it is treated for 5 min, to form a system containing the weakly acidified magnetic powder.
• BW-231 zinc-based phosphating solution of Enthusiasm Company is added to the above system, the added amount is based on the pH value, the pH value is adjusted to 4, the ultrasonic vibration is continuously performed, the power is controlled to 1500 W, and the treatment time is 15 min, to form a system containing the phosphating magnetic powder.
• the coupling agent is continuously added to the system, the ultrasonic vibration is performed, and the power is controlled to 1500 W, after 10 min, the system is vacuum-dried at 80°C for 5 h, to obtain the rare earth magnetic powder after the surface treatment.
• the rare earth magnetic powder after the surface treatment is mixed with the binder and granulated by using a double-screw extruder, and the granulating temperature is set at 200-220°C, to obtain the high-performance injection molding rare earth magnetic material.
• oxalic acid isopropanol solution 0.01 mol/L of oxalic acid isopropanol solution is dissolved in absolute ethanol, a pH value is adjusted to 7, to form weak acid solution; rare earth magnetic powder is added to it, the weak acid solution may completely wrap the magnetic powder, and its volume ratio to the magnetic powder is 2:1; ultrasonic vibration is turned on, the power is controlled to 2000 W, and it is treated for 5 min, to form a system containing the weakly acidified magnetic powder.
• BW-231 zinc-based phosphating solution of Enthusiasm Company is added to the above system, the added amount is based on the pH value, the pH value is adjusted to 5, the ultrasonic vibration is continuously performed, the power is controlled to 1500 W, and the treatment time is 15 min, to form a system containing the phosphating magnetic powder.
• the coupling agent is continuously added to the system, the ultrasonic vibration is performed, and the power is controlled to 1500 W, after 10 min, the system is vacuum-dried at 80°C for 5 h, to obtain the rare earth magnetic powder after the surface treatment.
• the rare earth magnetic powder after the surface treatment is mixed with the binder and granulated by using a double-screw extruder, and the granulating temperature is set at 290-310°C, to obtain the high-performance injection molding rare earth magnetic material.
• oxalic acid isopropanol solution 0.01 mol/L of oxalic acid isopropanol solution is dissolved in absolute ethanol, a pH value is adjusted to 7, to form weak acid solution; rare earth magnetic powder is added to it, the weak acid solution may completely wrap the magnetic powder, and its volume ratio to the magnetic powder is 3:1; ultrasonic vibration is turned on, the power is controlled to 2000 W, and it is treated for 5 min, to form a system containing the weakly acidified magnetic powder.
• BW-231 zinc-based phosphating solution of Enthusiasm Company is added to the above system, the added amount is based on the pH value, the pH value is adjusted to 5, the ultrasonic vibration is continuously performed, the power is controlled to 1500 W, and the treatment time is 15 min, to form a system containing the phosphating magnetic powder.
• the coupling agent is continuously added to the system, the ultrasonic vibration is performed, and the power is controlled to 1500 W, after 10 min, the system is vacuum-dried at 80°C for 5 h, to obtain the rare earth magnetic powder after the surface treatment.
• the rare earth magnetic powder after the surface treatment is mixed with the binder and granulated by using a double-screw extruder, and the granulating temperature is set at 200-220°C, to obtain the high-performance injection molding rare earth magnetic material.
• oxalic acid isopropanol solution 0.01 mol/L of oxalic acid isopropanol solution is dissolved in absolute ethanol, a pH value is adjusted to 6, to form weak acid solution; rare earth magnetic powder is added to it, the weak acid solution may completely wrap the magnetic powder, and its volume ratio to the magnetic powder is 1.5:1; ultrasonic vibration is turned on, the power is controlled to 2000 W, and it is treated for 5 min, to form a system containing the weakly acidified magnetic powder.
• BW-231 zinc-based phosphating solution of Enthusiasm Company is added to the above system, the added amount is based on the pH value, the pH value is adjusted to 5, the ultrasonic vibration is continuously performed, the power is controlled to 1500 W, and the treatment time is 15 min, to form a system containing the phosphating magnetic powder.
• the coupling agent is continuously added to the system, the ultrasonic vibration is performed, and the power is controlled to 1500 W, after 10 min, the system is vacuum-dried at 80°C for 5 h, to obtain the rare earth magnetic powder after the surface treatment.
• the rare earth magnetic powder after the surface treatment is mixed with the binder and granulated by using a double-screw extruder, and the granulating temperature is set at 290-310°C, to obtain the high-performance injection molding rare earth magnetic material.
• Embodiment 1 A different from Embodiment 1 is only that the weak acid is a carbonic acid, and the silane coupling agent is KH792.
• Embodiment 1 A different from Embodiment 1 is only that: Ethanol is used to adjust a pH value of weak acid solution to 7, and the volume ratio of the weak acid solution to the rare earth magnetic powder is 3:1; the power of the first ultrasonic vibration is 1500 W, and it is treated for 2 min.
• Zinc-based phosphating solution is added to a system containing weakly acidified magnetic powder, the pH value is adjusted to 5, the ultrasonic vibration is continuously performed, the power is controlled to 1000 W, and the treatment time is 10 min, to form a system containing the phosphating magnetic powder.
• a coupling agent is continuously added to the system, the added amount of the coupling agent is 0.5% of the weight of the rare earth magnetic powder, the ultrasonic vibration is performed, and the power is controlled to 2000 W, after 15 min, the system is vacuum-dried at 90°C for 5 h, to obtain the rare earth magnetic powder after the surface treatment.
• Embodiment 1 A different from Embodiment 1 is only that: Ethanol is used to adjust a pH value of weak acid solution to 6, and the volume ratio of the weak acid solution to the rare earth magnetic powder is 2:1; the power of the first ultrasonic vibration is 2500 W, and it is treated for 4 min.
• Zinc-based phosphating solution is added to a system containing weakly acidified magnetic powder, the pH value is adjusted to 5, the ultrasonic vibration is continuously performed, the power is controlled to 1500 W, and the treatment time is 15 min, to form a system containing the phosphating magnetic powder.
• a coupling agent is continuously added to the system, the added amount of the coupling agent is 1% of the weight of the rare earth magnetic powder, the ultrasonic vibration is performed, and the power is controlled to 1200 W, after 15 min, the system is vacuum-dried at 90°C for 7 h, to obtain the rare earth magnetic powder after the surface treatment.
• the silane coupling agent and the phosphoric acid are dissolved in an appropriate amount of anhydrous ethanol, the rare earth magnetic powder is added to it, the amount of the anhydrous ethanol is enough to completely wrap the magnetic powder, and its volume ratio to the magnetic powder is 1.5:1; and then the rare earth magnetic powder is added to the solution, it is fully stirred and mixed uniformly, and then vacuum-dried at 80°C for 5 h, to obtain the rare earth magnetic powder after the surface treatment.
• the rare earth magnetic powder after the surface treatment is mixed with the binder and granulated by using a double-screw extruder, and the granulating temperature is set at 200-220°C, to obtain the injection molding rare earth magnetic material.
• the silane coupling agent and the phosphoric acid are dissolved in an appropriate amount of anhydrous ethanol, the rare earth magnetic powder is added to it, the amount of the anhydrous ethanol is enough to completely wrap the magnetic powder, and its volume ratio to the magnetic powder is 2:1; and then the rare earth magnetic powder is added to the solution, it is fully stirred and mixed uniformly, and then vacuum-dried at 80°C for 5 h, to obtain the rare earth magnetic powder after the surface treatment.
• the rare earth magnetic powder after the surface treatment is mixed with the binder and granulated by using a double-screw extruder, and the granulating temperature is set at 290-310°C, to obtain the injection molding rare earth magnetic material.
• the silane coupling agent and the phosphoric acid are dissolved in an appropriate amount of anhydrous ethanol, the rare earth magnetic powder is added to it, the amount of the anhydrous ethanol is enough to completely wrap the magnetic powder, and its volume ratio to the magnetic powder is 3:1; and then the rare earth magnetic powder is added to the solution, it is fully stirred and mixed uniformly, and then vacuum-dried at 80°C for 5 h, to obtain the rare earth magnetic powder after the surface treatment.
• the rare earth magnetic powder after the surface treatment is mixed with the binder and granulated by using a double-screw extruder, and the granulating temperature is set at 200-220°C, to obtain the injection molding rare earth magnetic material.
• the silane coupling agent and the phosphoric acid are dissolved in an appropriate amount of anhydrous ethanol, the rare earth magnetic powder is added to it, the amount of the anhydrous ethanol is enough to completely wrap the magnetic powder, and its volume ratio to the magnetic powder is 1.5:1; and then the rare earth magnetic powder is added to the solution, it is fully stirred and mixed uniformly, and then vacuum-dried at 80°C for 5 h, to obtain the rare earth magnetic powder after the surface treatment.
• the rare earth magnetic powder after the surface treatment is mixed with the binder and granulated by using a double-screw extruder, and the granulating temperature is set at 290-310°C, to obtain the injection molding rare earth magnetic material.
• Br, Hcj, and (BH) max are all important indicators of the magnetic performance of the permanent magnet material. After the rare earth permanent magnet material is oxidized, the performance is decreased, and these indicators may be decreased accordingly. The oxidation is more severe, and these indicators are decreased more. It may be seen from the above table that the Br, Hcj, and (BH) max indicators of the injection molding rare earth magnetic material prepared by using the rare earth magnetic powder treated by the surface treatment method in the embodiment of the present disclosure are significantly improved, it is indicated that the oxidation resistance thereof is stronger, and the magnetic performance of the injection molding rare earth magnetic material is better. It should be noted that for the different binders, there is a big difference in temperature during the injection molding, and the preparation of the magnetic powder at different temperatures may bring about a larger difference.
• the differences between the performances of the rare earth magnetic powder injection molding materials prepared in the above Embodiments 1 to 4 are significant. However, it is respectively compared with Contrast examples 1 to 4, the performance of the injection molding material corresponding to the same binder or the same magnetic powder is significantly improved, and it is sufficient to indicate the beneficial effects brought by the surface treatment method of the present disclosure.
• Fluidity refers to a melt flow rate of a finished product under a certain pressure and a certain molten state. Magnetic powder agglomeration or irregular morphology of the magnetic powder may affect the fluidity. It may be seen from the above table that the melt index of the injection molding rare earth magnetic material prepared by using the surface treatment method in the embodiment of the present disclosure is significantly improved, and it is indicated that the rare earth magnetic powder has the more regular morphology, and the compatibility with the binder after the surface treatment is better.

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• 2021
  • 2021-10-27 CN CN202111258526.6A patent/CN116031055A/zh active Pending
  • 2021-11-05 EP EP21827559.2A patent/EP4199016A4/fr active Pending
  • 2021-11-05 WO PCT/CN2021/129091 patent/WO2023070735A1/fr unknown

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