Method for preparing neodymium-iron-boron permanent magnetic material

Abstract

A method for preparing a NdFeB permanent magnetic material may include providing a covered NdFeB magnetic powder by depositing heavy rare earth particles or high-melting particles onto a NdFeB magnetic powder by physical vapor deposition; and performing orientation molding and sintering on the covered NdFeB magnetic powder to provide the NdFeB permanent magnetic material.

Claims

1. A method for preparing a NdFeB permanent magnetic material, the method comprising: (1) carrying out ingredients-mixing, smelting, strip casting, hydrogen crushing, disproportionation reaction, and jet milling to obtain NdFeB fine powder with an average particle diameter D50 of 1 μm; (2) placing the NdFeB fine powder and a CoZr thermal resistance wire respectively in a thermal resistance evaporation deposition device with a vacuum degree of 10.sup.3 Pa; setting parameters so as to uniformly disperse the NdFeB fine powder; heating the CoZr thermal resistance wire to evaporate and deposit CoZr particles on the NdFeB fine powder; taking out the covered NdFeB fine powder after its temperature is decreased to room temperature; (3) performing orientation molding, sintering, and heat treatment on the covered NdFeB fine powder so as to obtain the NdFeB permanent magnetic material.

Description

PREFERRED EMBODIMENTS OF THIS DISCLOSURE

(1) The technical solution of this disclosure will be described in details below with reference to example embodiments. However, the example embodiments can be performed in a variety of forms, they should not be construed as being limited to the embodiments set forth herein; rather, these embodiments are provided to make this disclosure more comprehensive and complete, and fully convey the concept of the example embodiments to those skilled in the art.

(2) The invention is applied to preparing NdFeB magnets, NdFeB sheets, NdFeB magnetic powders, and NdFeB fine powders.

(3) Scheme 1:

(4) A method for preparing an NdFeB magnet with a low amount of heavy rare earth, where the NdFeB magnet has a high coercive force, the specific steps are as follows:

(5) Step 1: preparing an NdFeB magnetic powder, and depositing a trace amount of heavy rare earth particles or high-melting particles onto the NdFeB magnetic powder by physical vapor deposition;

(6) Mixing ingredients, smelting, strip casting, crushing and milling the NdFeB sheets into powder, coating the NdFeB powder by depositing heavy rare earth particles, performing orientation molding; performing physical vapor deposition in an inert atmosphere where the temperature is 300-500° C. and the deposition rate is 0.01-50 μm/min.

(7) Step 2: Sintering to prepare an NdFeB magnet.

(8) The heavy rare earth particles or the high-melting particles can be uniformly dispersed at grain boundaries in the magnet, so that the coercive force of the magnet is increased, the crystal grains in the magnet are refined, the amount of heavy rare earth is reduced, and the remanence and magnetic energy product remains excellent.

(9) Routine 1 of the Preparation of an NdFeB Magnet by Sintering

(10) Step 11: mixing ingredients, smelting, strip casting, crushing and milling the NdFeB sheets into powder, so as to prepare NdFeB magnetic powder with a diameter of 1-20 μm;

(11) Step 12: selecting a desired heavy rare earth target, and placing the NdFeB magnetic powder and the heavy rare earth target in a physical vapor deposition device, respectively;

(12) The heavy rare earth target is at least one selected from pure metal, alloy or oxide of Dy, Tb or Dy-Tb.

(13) Step 13: performing physical vapor deposition in an inert atmosphere (argon or helium or vacuum) to deposit heavy rare earth element (Dy or Tb) particles onto the NdFeB magnetic powder;

(14) Evacuating the chamber to a vacuum degree lower than 2.0×10.sup.−2 Pa, charging an inert gas (argon, argon or helium) to 0.2-1.0 Pa; adjusting the parameters to uniformly disperse the NdFeB magnetic powder while heating magnetic powder to a temperature of 300-500° C.; depositing target particles onto the dispersed NdFeB magnetic powder with a particle deposition rate of 0.01-50 μm/min.

(15) The physical vapor deposition includes magnetron sputtering deposition, ion plating deposition, and evaporation source deposition.

(16) Step 14: terminating the physical vapor deposition, and taking out the NdFeB magnetic powder after its temperature decreases to room temperature.

(17) Step 15: performing orientation compression molding, sintering in the vacuum and annealing treatment on the obtained magnetic powder, so as to obtain a final NdFeB magnet.

(18) Routine 2 of the Preparation of an NdFeB Magnet by Sintering

(19) Step 21: mixing ingredients, smelting, strip casting, crushing and milling the NdFeB sheets into powder, so as to prepare NdFeB magnetic powder with a diameter of 1-20 μm;

(20) Step 22: selecting a desired high-melting target material, and placing the NdFeB magnetic powder and the high-melting target material in a physical vapor deposition device, respectively;

(21) The high-melting target material is at least one selected from pure metal, alloy or oxide of elements, such as, W, Mo, V, Ti, Ta, Zr, Nb, Co, Cr, Ga.

(22) Step 23: depositing the high-melting element (W, Mo, V, Ti, Ta, Zr, Nb, Co, Cr or Ga) particles onto the NdFeB magnetic powder in an inert atmosphere;

(23) Evacuating the chamber to a vacuum degree lower than 2.0×10.sup.−2 Pa, charging an inert gas (argon, helium or vacuum) to 0.2-1.0 Pa; uniformly dispersing the NdFeB magnetic powder while heating magnetic powder with a temperature of 300-500° C.; depositing target particles onto the dispersed NdFeB magnetic powder with a particle deposition rate of 0.01-50 μm/min.

(24) The physical vapor deposition comprises magnetron sputtering deposition, ion plating deposition, and evaporation source deposition.

(25) Step 24: terminating the physical vapor deposition, and taking out the NdFeB magnetic powder after its temperature decreases to room temperature.

(26) Step 25: performing orientation compression molding, sintering in the vacuum and annealing treatment on the obtained magnetic powder, so as to obtain a final NdFeB magnet.

Example 1

(27) (1) Ingredients-mixing, smelting, strip casting, disc crushing and ball milling were performed, so as to obtain magnetic powder of NdFeB alloy with an average particle size of 3.5 μm;

(28) (2) Physical vapor deposition was carried out on the magnetic powder obtained in the step (1);

(29) Dy metal target material was selected, the chamber was evacuated to a vacuum degree of 2.0×10.sup.−2 Pa, argon was charged to 0.2 Pa; the magnetic powder was heated to 380° C., magnetron sputtering was carried out with the sputtering power adjusted to get Dy particle deposition rate of 0.01 μm/min, and the magnetic powder was taken out after its temperature decreased to room temperature;

(30) (3) Orientation molding, sintering and heat treatment were performed on the magnetic powder obtained in the step (2), so as to obtain a final NdFeB magnet.

(31) The magnetic energy product and the coercive force of the magnet prepared in this example were tested with a magnetic property measuring instruments, and compared with the magnet prepared by the conventional method. The results are shown in Table 1.

(32) TABLE-US-00001 TABLE 1 Intrinsic coercive Maximum magnetic Remanence/ force/ energy product/ Samples kGs kOe MGOe NdFeB 12.62 18.39 37.51 NdFeB—Dy 12.55 22.83 37.80

Example 2

(33) (1) Ingredients-mixing, smelting, strip casting, hydrogen crushing and jet milling were performed, so as to obtain magnetic powder of NdFeB alloy with an average particle size of 4.1 μm;

(34) (2) Physical vapor deposition was carried out on the magnetic powder obtained in the step (1);

(35) Tb metal target material was selected, the chamber was evacuated to a vacuum degree of 5.0×10.sup.−3 Pa, helium was charged till the vacuum degree reached 0.5 Pa; the magnetic powder was heated to 420° C., ion plating (the atoms from the target material are mostly in an ion state with a higher energy, leading to a better combination with the surface of the NdFeB magnetic powder) was performed. The current of the argon source was adjusted so that the deposition rate of the Tb particles was 50 μm/min, and the NdFeB magnetic powder was taken out after its temperature decreased to room temperature;

(36) (3) Orientation molding, sintering and heat treatment were performed on the magnetic powder obtained in the step (2), so as to obtain a final NdFeB magnet.

(37) The magnetic energy product and the coercive force of the magnet prepared in this example were tested with a magnetic property measuring instruments, and compared with the magnet prepared by the conventional method. The results are shown in Table 2.

(38) TABLE-US-00002 TABLE 2 Intrinsic coercive Maximum magnetic Remanence/ force/ energy product/ Samples kGs kOe MGOe NdFeB 13.48 19.36 42.97 NdFeB—Tb 13.13 28.45 41.62

Example 3

(39) (1) Ingredients-mixing, smelting, strip casting, hydrogen crushing and jet milling were performed, so as to obtain magnetic powder of NdFeB alloy with an average particle size of 3.7 μm;

(40) (2) Physical vapor deposition was performed on the magnetic powder obtained in the step (1);

(41) CoZr metal target material was selected, the chamber was evacuated to a vacuum degree of 9.0×10.sup.−4 Pa, the magnetic powder was heated to 300° C., vapor deposition was carried out with the heating source power of the evaporation boat adjusted to get CoZr atoms vaporized and evaporated at a deposition rate of 3 μm/min, and the NdFeB magnetic powder was taken out after its temperature decreased to room temperature;

(42) (3) Orientation molding, sintering and heat treatment were performed on the magnetic powder obtained in the step (2), so as to obtain a final NdFeB magnet.

(43) The magnetic energy product and the coercive force of the magnet prepared in this example were tested with a magnetic property measuring instruments, and compared with the magnet prepared by the conventional method. The results are shown in Table 3.

(44) TABLE-US-00003 TABLE 3 Intrinsic coercive Maximum magnetic Remanence/ force/ energy product/ Samples kGs kOe MGOe NdFeB 13.18 19.80 41.75 NdFeB—CoZr 12.97 22.38 40.70

Example 4

(45) (1) Ingredients-mixing, smelting, strip casting, hydrogen crushing and jet milling were performed, so as to obtain magnetic powder of NdFeB alloy with an average particle size of 4.3 μm;

(46) (2) Physical vapor deposition was performed on the magnetic powder obtained in the step (1);

(47) Dy.sub.2O.sub.3 target material and Mo target material were selected, the chamber was evacuated to a vacuum degree of 3.0×10.sup.−2 Pa, argon was charged till the vacuum degree reached 0.3 Pa, the magnetic powder was heated to 500° C., magnetron sputtering was simultaneously performed on both kinds of targets with the sputtering power adjusted to get the particle deposition rate of 0.2 μm/min, and the NdFeB magnetic powder was taken out after its temperature decreased to room temperature;

(48) (3) Orientation molding, sintering and heat treatment were performed on the magnetic powder obtained in the step (2), so as to obtain a final NdFeB magnet.

(49) The magnetic energy product and the coercive force of the magnet prepared in this example were tested with a magnetic property measuring instruments, and compared with the magnet prepared by the conventional method. The results are shown in Table 4.

(50) TABLE-US-00004 TABLE 4 Intrinsic coercive Maximum magnetic Remanence/ force/ energy product/ Samples kGs kOe MGOe NdFeB 13.32 19.43 42.13 NdFeBDyMo 13.18 25.59 41.65

(51) Scheme 2:

(52) A method for preparing an NdFeB magnet with a low amount of heavy rare earth and high coercive force, which can uniformly disperse heavy rare earth particles or high-melting particles at grain boundaries in a magnet, leading to an improved coercive force, refined crystal grains in the magnet, and a reduction in the amount of heavy rare earth, with excellent remanence and magnetic energy product.

(53) The specific steps are as follows:

(54) Step 1: preparing an NdFeB coarse powder, and depositing a trace amount of heavy rare earth particles or high-melting particles onto the NdFeB coarse powder by physical vapor deposition;

(55) Mixing ingredients, smelting, strip casting, coarse crushing the NdFeB sheets into NdFeB coarse powder; during the physical vapor deposition process, an inert atmosphere (argon, helium or vacuum) is utilized, the temperature is 300-500° C., and the deposition rate is 0.01-50 μm/min.

(56) Step 2: performing fine powder milling, orientation molding, and sintering to prepare an NdFeB magnet.

(57) Routine 1: Deposition of Heavy Rare Earth Particles

(58) Step 11: mixing ingredients, smelting, strip casting, coarse crushing to prepare NdFeB coarse powder;

(59) The NdFeB coarse powder has a particle size of 10 μm-2 mm, and the coarse crushing is mechanical crushing or hydrogen crushing.

(60) Step 12: selecting a desired heavy rare earth target material, and placing the NdFeB coarse powder and the heavy rare earth target material in a physical vapor deposition device, respectively.

(61) The heavy rare earth target material is selected from pure metal of Dy, Tb, or alloy of Dy-Tb, or oxides of Dy, Tb. The physical vapor deposition method is selected from magnetron sputtering deposition, ion plating deposition or evaporation source deposition.

(62) Step 13: evacuating the chamber to a degree of vacuum lower than 2.0×10.sup.−2 Pa, charging argon to 0.2-1.0 Pa;

(63) Step 14: adjusting the parameters to uniformly disperse the NdFeB coarse powder while heating the magnetic powder to 300-500° C.;

(64) Step 15: turning on the physical vapor deposition device to deposit the particles of the target onto the dispersed NdFeB coarse powder with a particle deposition rate of 0.01-50 μm/min;

(65) Step 16: terminating the physical vapor deposition, and taking out the coarse powder after its temperature decreases to room temperature.

(66) Step 17: performing fine powder milling, orientation compression molding, sintering in the vacuum, and annealing treatment to obtain a final NdFeB magnet.

(67) Routine 2: Deposition of High-Melting Particles

(68) Step 21: mixing ingredients, smelting, strip casting, coarse crushing to prepare NdFeB coarse powder;

(69) The coarse NdFeB powder has a particle size of 10 μm-2 mm, and the coarse crushing is mechanical crushing or hydrogen crushing.

(70) Step 22: selecting a desired high-melting target material, and placing the NdFeB coarse powder and the high-melting target material in a physical vapor deposition device, respectively;

(71) Selecting at least one pure metal, alloy or oxide from the following as the high-melting target material: W, Mo, V, Ti, Ta, Zr, Nb, Co, Cr, Ga and the like. Selecting from the following as physical vapor deposition: magnetron sputtering deposition, ion plating deposition or evaporation source deposition.

(72) Step 23: evacuating the chamber to a degree of vacuum lower than 2.0×10.sup.−2 Pa, charging argon to 0.2-1.0 Pa;

(73) Step 24: adjusting the parameters to uniformly disperse the NdFeB coarse powder while heating the magnetic powder to 300-500° C.;

(74) Step 25: turning on the physical vapor deposition device to deposit the particles of the target onto the dispersed NdFeB coarse powder;

(75) The particle deposition rate is 0.01-50 μm/min;

(76) Step 26: terminating the physical vapor deposition, and taking out the NdFeB coarse powder after its temperature decreases to room temperature.

(77) Step 27: performing fine powder milling, orientation compression molding, sintering in the vacuum, and annealing treatment on the obtained NdFeB coarse powder to obtain a final NdFeB magnet.

Example 5

(78) (1) Ingredients-mixing, smelting, strip casting, coarse crushing with disc grinding were carried out;

(79) (2) Physical vapor deposition was performed on the obtained NdFeB coarse powder:

(80) Dy metal target material was selected, the chamber was evacuated to a vacuum degree of 2.0×10.sup.−2 Pa, argon was charged to 0.2 Pa, magnetron sputtering was carried out with the sputtering power adjusted to get Dy particle deposition rate of 0.01 μm/min;

(81) (3) Ball milling, orientation molding, sintering and heat treatment were performed on the obtained NdFeB coarse powder, so as to obtain a final NdFeB magnet.

(82) The magnetic energy product and the coercive force of the magnet prepared in this example were tested with a magnetic property measuring instruments, and compared with the magnet prepared by the conventional method. The results are shown in Table 5.

(83) TABLE-US-00005 TABLE 5 Intrinsic coercive Maximum magnetic Remanence/ force/ energy product/ Samples kGs kOe MGOe NdFeB 12.62 18.39 37.51 NdFeB—Dy 12.55 22.83 37.80

Example 6

(84) (1) Ingredients-mixing, smelting, strip casting, hydrogen crushing were carried out;

(85) (2) Physical vapor deposition was performed on the obtained NdFeB coarse powder:

(86) Tb metal target material was selected, the chamber was evacuated to a vacuum degree of 5.0×10.sup.−3 Pa, argon was charged to 0.5 Pa

(87) The NdFeB coarse powder was heated to 300° C., ion plating was carried out with the current of the argon source adjusted, so that the deposition rate of the Tb particles is 50 μm/min;

(88) (3) Jet milling, orientation molding, sintering and heat treatment were performed on the obtained NdFeB coarse powder, so as to obtain a final NdFeB magnet.

(89) The magnetic energy product and the coercive force of the magnet prepared in this example were tested with a magnetic property measuring instruments, and compared with the magnet prepared by the conventional method. The results are shown in Table 6.

(90) TABLE-US-00006 TABLE 6 Intrinsic coercive Maximum magnetic Remanence/ force/ energy product/ Samples kGs kOe MGOe NdFeB 13.48 19.36 42.97 NdFeB—Tb 13.13 28.45 41.62

Example 7

(91) (1) Ingredients-mixing, smelting, strip casting, hydrogen crushing were carried out;

(92) (2) Physical vapor deposition was performed on the obtained NdFeB coarse powder:

(93) CoZr metal target material was selected, the chamber was evacuated to a vacuum degree of 9.0×10.sup.−4 Pa, the NdFeB coarse powder was heated to 500° C., The vapor deposition was carried out with the heating source power of the evaporation boat adjusted to get CoZr atoms vaporized and evaporated at a deposition rate of 3 μm/min;

(94) (3) Jet milling, orientation molding, sintering and heat treatment were performed on the obtained NdFeB coarse powder, so as to obtain a final NdFeB magnet.

(95) The magnetic energy product and the coercive force of the magnet prepared in this example were tested with a magnetic property measuring instruments, and compared with the magnet prepared by the conventional method. The results are shown in Table 7.

(96) TABLE-US-00007 TABLE 7 Intrinsic coercive Maximum magnetic Remanence/ force/ energy product/ Samples kGs kOe MGOe NdFeB 13.18 19.80 41.75 NdFeB—CoZr 12.97 22.38 40.70

Example 8

(97) (1) Ingredients-mixing, smelting, strip casting, hydrogen crushing were carried out;

(98) (2) Physical vapor deposition was performed on the obtained NdFeB coarse powder:

(99) Dy.sub.2O.sub.3 target material, Mo target material were selected, the chamber was evacuated to a vacuum degree of 3.0×10.sup.−2 Pa, argon was charged to 0.3 Pa, the NdFeB coarse powder was heated to 420° C., magnetron sputtering was simultaneously performed on both kinds of targets with the sputtering power adjusted to get the particle deposition rate of 0.2 μm/min;

(100) (3) Jet milling, orientation molding, sintering and heat treatment were performed on the obtained NdFeB coarse powder, so as to obtain a final NdFeB magnet.

(101) The magnetic energy product and the coercive force of the magnet prepared in this example were tested with a magnetic property measuring instruments, and compared with the magnet prepared by the conventional method. The results are shown in Table 8.

(102) TABLE-US-00008 TABLE 8 Intrinsic coercive Maximum magnetic Remanence/ force/ energy product/ Samples kGs kOe MGOe NdFeB 13.32 19.43 42.13 NdFeB—DyMo 13.18 25.59 41.65

(103) Scheme 3:

(104) A method for preparing an NdFeB magnet with a low amount of heavy rare earth but high coercive force, the specific steps are as follows:

(105) Step 1: mixing ingredients, smelting, strip casting;

(106) Step 2: carrying out physical vapor deposition method in an inert atmosphere to deposit the target particles (a trace amount of heavy rare earth particles or high-melting particles) onto the NdFeB sheets;

(107) The target particles of the physical vapor deposition are selected from the group consisting of particles of heavy rare earth elements Dy or Tb, or high-melting particles of one or more elements of W, Mo, V, Ti, Ta, Zr, Nb, Co, Cr, Ga. The inert atmosphere is argon or helium or vacuum.

(108) Step 3: further, the NdFeB magnet is prepared by crushing and sintering.

(109) Routine 1: Deposition of a Trace Amount of Heavy Rare Earth Particles

(110) Step 11: mixing ingredients, smelting, strip casting;

(111) Step 12: selecting a desired heavy rare earth target material;

(112) Step 13: placing the NdFeB alloy sheets and the heavy rare earth target material in a physical vapor deposition device, respectively;

(113) The heavy rare earth target material is at least one selected from the group of pure metal, alloy or oxide of Dy, Tb or Dy-Tb.

(114) Step 14: evacuating the chamber to a vacuum degree lower than 2.0×10.sup.−2 Pa, charging argon to 0.2-1.0 Pa;

(115) Step 15: adjusting the parameters, heating the NdFeB sheets, where the heating temperature is 300-500° C.;

(116) Step 16: turning on the physical vapor deposition device to deposit the particles of the target onto the NdFeB sheets by the physical vapor deposition;

(117) The physical vapor deposition includes magnetron sputtering deposition, ion plating deposition, and evaporation source deposition. The particle deposition rate is 0.01-50 μm/min.

(118) Step 17: terminating the physical vapor deposition, and taking out the NdFeB sheets after their temperature decreases to room temperature;

(119) Step 18: crushing the obtained NdFeB sheets into powder, and performing orientation compression molding, sintering in the vacuum and annealing treatment, so as to obtain a final NdFeB magnet.

(120) Routine 2: Deposition of High-Melting Particles

(121) Step 21: mixing ingredients, smelting, strip casting;

(122) Step 22: selecting a desired high-melting target material;

(123) Step 23: placing the NdFeB alloy sheets and the high-melting target material in a physical vapor deposition device, respectively;

(124) The high-melting target material is at least one selected from the group of pure metal, alloy or oxide of elements W, Mo, V, Ti, Ta, Zr, Nb, Co, Cr, Ga and the like.

(125) Step 24: evacuating the chamber to a degree of vacuum lower than 2.0×10.sup.−2 Pa, charging argon to 0.2-1.0 Pa;

(126) Step 25: adjusting the parameters to heat the NdFeB sheets, where the heating temperature is 300-500° C.;

(127) Step 26: turning on the physical vapor deposition device to deposit the particles of the target onto the NdFeB sheets by the physical vapor deposition;

(128) The physical vapor deposition includes magnetron sputtering deposition, ion plating deposition, and evaporation source deposition. The particle deposition rate is 0.01-50 μm/min.

(129) Step 27: terminating the physical vapor deposition, and taking out the NdFeB sheets after their temperature decreases to room temperature;

(130) Step 28: crushing the prepared NdFeB sheets into powder, and performing orientation compression molding, sintering in the vacuum and annealing treatment, so as to obtain a final NdFeB magnet.

Example 9

(131) (1) Ingredients-mixing, smelting, strip casting were carried out to prepare NdFeB sheets;

(132) (2) Physical vapor deposition was performed on the obtained NdFeB sheets:

(133) Dy metal target material was selected, the chamber was evacuated to a vacuum degree of 2.0×10.sup.−2 Pa, argon was charged to 0.2 Pa, magnetron sputtering was carried out with the sputtering power adjusted to get Dy particle deposition rate of 0.01 μm/min;

(134) (3) Disc crushing, ball milling, orientation molding, sintering and heat treatment were performed on the obtained NdFeB sheets, so as to obtain a final NdFeB magnet.

(135) The magnetic energy product and the coercive force of the magnet prepared in this example were tested with a magnetic property measuring instruments, and compared with the magnet prepared by the conventional method. The results are shown in Table 9.

(136) TABLE-US-00009 TABLE 9 Intrinsic coercive Maximum magnetic Remanence/ force/ energy product/ Samples kGs kOe MGOe NdFeB 12.62 18.39 37.51 NdFeB—Dy 12.55 22.83 37.80

Example 10

(137) (1) Ingredients-mixing, smelting, strip casting were carried out to prepare NdFeB sheets;

(138) (2) Physical vapor deposition was performed on the obtained NdFeB sheets:

(139) Tb metal target material was selected, the chamber was evacuated to a vacuum degree of 5.0×10.sup.−3 Pa, helium was charged to 0.5 Pa, the NdFeB sheets were heated to 300° C., ion plating was carried out with the current of the argon source adjusted, so that the deposition rate of the Tb particles is 50 μm/min;

(140) (3) Hydrogen crushing, jet milling, orientation molding, sintering and heat treatment were performed on the obtained NdFeB sheets, so as to obtain a final NdFeB magnet.

(141) The magnetic energy product and the coercive force of the magnet prepared in this example were tested with a magnetic property measuring instruments, and compared with the magnet prepared by the conventional method. The results are shown in Table 10.

(142) TABLE-US-00010 TABLE 10 Intrinsic coercive Maximum magnetic Remanence/ force/ energy product/ Samples kGs kOe MGOe NdFeB 13.48 19.36 42.97 NdFeB—Tb 13.13 28.45 41.62

Example 11

(143) (1) Ingredients-mixing, smelting, strip casting were carried out to prepare NdFeB sheets;

(144) (2) Physical vapor deposition was performed on the obtained NdFeB sheets:

(145) CoZr metal target material was selected, the chamber was evacuated to a vacuum degree of 9.0×10.sup.−4 Pa, the NdFeB sheets were heated to 500° C.

(146) The vapor deposition was carried out with the heating source power of the evaporation boat adjusted to get CoZr atoms vaporized and evaporated at a deposition rate of 3 μm/min.

(147) (3) Hydrogen crushing, jet milling, orientation molding, sintering and heat treatment were performed on the obtained NdFeB sheets, so as to obtain a final NdFeB magnet.

(148) The magnetic energy product and the coercive force of the magnet prepared in this example were tested with a magnetic property measuring instruments, and compared with the magnet prepared by the conventional method. The results are shown in Table 11.

(149) TABLE-US-00011 TABLE 11 Intrinsic coercive Maximum magnetic Remanence/ force/ energy product/ Samples kGs kOe MGOe NdFeB 13.18 19.80 41.75 NdFeB—CoZr 12.97 22.38 40.70

Example 12

(150) (1) Ingredients-mixing, smelting, strip casting were carried out to prepare NdFeB sheets;

(151) (2) Physical vapor deposition was performed on the obtained NdFeB sheets:

(152) Dy.sub.2O.sub.3 target material, Mo target material were selected, the chamber was evacuated to a vacuum degree of 3.0×10.sup.−2 Pa, argon was charged to 0.3 Pa, the NdFeB sheets were heated to 420° C., magnetron sputtering was simultaneously performed on both kinds of targets with the sputtering power adjusted to get the particle deposition rate of 0.2 μm/min;

(153) (3) Hydrogen crushing, jet milling, orientation molding, sintering and heat treatment were performed on the obtained NdFeB sheets, so as to obtain a final NdFeB magnet.

(154) The magnetic energy product and the coercive force of the magnet prepared in this example were tested with a magnetic property measuring instruments, and compared with the magnet prepared by the conventional method. The results are shown in Table 12.

(155) TABLE-US-00012 TABLE 12 Intrinsic coercive Maximum magnetic Remanence/ force/ energy product/ Samples kGs kOe MGOe NdFeB 13.32 19.43 42.13 NdFeB—DyMo 13.18 25.59 41.65

(156) Scheme 4:

(157) A method for preparing a NdFeB sheets, comprising the specific steps as follows:

(158) Step 1: mixing the ingredients according to the formula, smelting and strip casting the mixture;

(159) Step 2: carrying out physical vapor deposition method to deposit the target particles onto the NdFeB sheets.

(160) The physical vapor deposition includes magnetron sputtering deposition, ion plating deposition, and evaporation source deposition. During the physical vapor deposition process, an inert atmosphere is utilized, the temperature is 300-500° C., and the deposition rate is 0.01-50 μm/min. The inert atmosphere is argon or helium or vacuum.

(161) Routine 1:

(162) Step 11: mixing the ingredients according to the formula, smelting and strip casting the mixture;

(163) Step 12: placing the NdFeB sheets and the target material of heavy rare earth in a physical vapor deposition device, respectively;

(164) The target material of heavy rare earth is at least one pure metal, alloy or oxide of Dy, Tb or Dy-Tb.

(165) Step 13: evacuating the chamber to a degree of vacuum lower than 2.0×10.sup.−2 Pa, charging argon to 0.2-1.0 Pa;

(166) Step 14: heating the NdFeB sheets with a heating temperature of 300-500° C.

(167) Step 15: turning on the physical vapor deposition device to deposit the heavy rare earth particles onto the NdFeB sheets by the physical vapor deposition;

(168) The physical vapor deposition includes magnetron sputtering deposition, ion plating deposition, and evaporation source deposition. The heavy rare earth particle deposition rate is 0.01-50 μm/min.

(169) Step 16: terminating the physical vapor deposition, and taking out the NdFeB sheets after their temperature decreases to room temperature.

(170) Routine 2:

(171) Step 21: mixing the ingredients according to the formula, smelting and strip casting the mixture;

(172) Step 22: placing the NdFeB sheets and the high-melting target material in a physical vapor deposition device, respectively;

(173) The high-melting target material is at least one pure metal, alloy or oxide of elements W, Mo, V, Ti, Ta, Zr, Nb, Co, Cr, Ga and the like.

(174) Step 23: evacuating the chamber to a degree of vacuum lower than 2.0×10.sup.−2 Pa, charging argon to 0.2-1.0 Pa;

(175) Step 24: heating the NdFeB sheets with a heating temperature of 300-500° C.

(176) Step 25: turning on the physical vapor deposition device to deposit the high-melting particles onto the NdFeB sheets by the physical vapor deposition;

(177) The physical vapor deposition includes magnetron sputtering deposition, ion plating deposition, and evaporation source deposition. The high-melting particles deposition rate is 0.01-50 μm/min.

(178) Step 26: terminating the physical vapor deposition, and taking out the NdFeB sheets after their temperature decreases to room temperature.

(179) The physical vapor deposition of the NdFeB sheets can be carried out simultaneously using Schemes 1 and 2.

Example 13

(180) (1) Ingredients-mixing, smelting, strip casting were carried out to prepare NdFeB sheets;

(181) (2) Physical vapor deposition was performed on the obtained NdFeB sheets:

(182) Dy metal target material was selected, the chamber was evacuated to a vacuum degree of 2.0×10.sup.−2 Pa, argon was charged to 0.2 Pa, magnetron sputtering was carried out with the sputtering power adjusted to get Dy particle deposition rate of 0.01 μm/min;

(183) (3) Disc crushing, ball milling, orientation molding, sintering and heat treatment were performed on the obtained NdFeB sheets, so as to obtain a final NdFeB magnet.

(184) The magnetic energy product and the coercive force of the magnet prepared in this example were tested with a magnetic property measuring instruments, and compared with the magnet prepared by the conventional method. The results are shown in Table 13.

(185) TABLE-US-00013 TABLE 13 Intrinsic coercive Maximum magnetic Remanence/ force/ energy product/ Samples kGs kOe MGOe NdFeB 12.62 18.39 37.51 NdFeB—Dy 12.55 22.83 37.80

Example 14

(186) (1) Ingredients-mixing, smelting, strip casting were carried out to prepare NdFeB sheets;

(187) (2) Physical vapor deposition was performed on the obtained NdFeB sheets:

(188) Tb metal target material was selected, the chamber was evacuated to a vacuum degree of 5.0×10.sup.−3 Pa, helium was charged to 0.5 Pa, the NdFeB sheets were heated to 300° C., ion plating was carried out with the current of the argon source adjusted, so that the deposition rate of the Tb particles is 50 μm/min;

(189) (3) Hydrogen crushing, jet milling, orientation molding, sintering and heat treatment were performed on the obtained NdFeB sheets, so as to obtain a final NdFeB magnet.

(190) The magnetic energy product and the coercive force of the magnet prepared in this example were tested with a magnetic property measuring instruments, and compared with the magnet prepared by the conventional method. The results are shown in Table 14.

(191) TABLE-US-00014 TABLE 14 Intrinsic coercive Maximum magnetic Remanence/ force/ energy product/ Samples kGs kOe MGOe NdFeB 13.48 19.36 42.97 NdFeB—Tb 13.13 28.45 41.62

Example 15

(192) (1) Ingredients-mixing, smelting, strip casting were carried out to prepare NdFeB sheets;

(193) (2) Physical vapor deposition was performed on the obtained NdFeB sheets:

(194) CoZr metal target material was selected, the chamber was evacuated to a vacuum degree of 9.0×10.sup.−4 Pa, the NdFeB sheets were heated to 500° C.

(195) The vapor deposition was carried out with the heating source power of the evaporation boat adjusted to get CoZr atoms vaporized and evaporated at a deposition rate of 3 μm/min.

(196) (3) Hydrogen crushing, jet milling, orientation molding, sintering and heat treatment were performed on the obtained NdFeB sheets, so as to obtain a final NdFeB magnet.

(197) The magnetic energy product and the coercive force of the magnet prepared in this example were tested with a magnetic property measuring instruments, and compared with the magnet prepared by the conventional method. The results are shown in Table 15.

(198) TABLE-US-00015 TABLE 15 Intrinsic coercive Maximum magnetic Remanence/ force/ energy product/ Samples kGs kOe MGOe NdFeB 13.18 19.80 41.75 NdFeB—CoZr 12.97 22.38 41.70

Example 16

(199) (1) Ingredients-mixing, smelting, strip casting were carried out to prepare NdFeB sheets;

(200) (2) Physical vapor deposition was performed on the obtained NdFeB sheets:

(201) Dy.sub.2O.sub.3 target material and Mo target material were selected, the chamber was evacuated to a vacuum degree of 3.0×10.sup.−2 Pa, argon was charged to 0.3 Pa.

(202) The NdFeB sheets were heated to 420° C., magnetron sputtering was simultaneously performed on both kinds of targets with the sputtering power adjusted to get the particle deposition rate of 0.2 μm/min;

(203) (3) Hydrogen crushing, jet milling, orientation molding, sintering and heat treatment were performed on the obtained NdFeB sheets, so as to obtain a final NdFeB magnet.

(204) The magnetic energy product and the coercive force of the magnet prepared in this example were tested with a magnetic property measuring instruments, and compared with the magnet prepared by the conventional method. The results are shown in Table 16.

(205) TABLE-US-00016 TABLE 16 Intrinsic coercive Maximum magnetic Remanence/ force/ energy product/ Samples kGs kOe MGOe NdFeB 13.32 19.43 42.13 NdFeB-deposition 13.18 25.59 41.65

(206) Scheme 5:

(207) A method for preparing NdFeB magnetic powder, comprising the specific steps as follows:

(208) Step 1: preparing NdFeB magnetic powder of 1 μm-2 mm;

(209) After smelting and casting, the NdFeB magnet is mechanically crushed, or hydrogen crushed, or crushed in an air jet mill to prepare NdFeB magnetic powder.

(210) Step 2: selecting a desired high-melting target material, placing the NdFeB magnetic powder and the high-melting target material in a physical vapor deposition device, respectively;

(211) The high-melting target material is at least one pure metal, alloy or oxide of W, Mo, V, Ti, Ta, Zr, Nb, Co, Cr, Ga.

(212) Step 3: evacuating the chamber to a degree of vacuum lower than 2.0×10.sup.−2 Pa, charging argon to 0.2-1.0 Pa;

(213) Step 4: adjusting the parameters to uniformly disperse the NdFeB magnetic powder while heating the NdFeB magnetic powder, where the heating temperature is 300-500° C.;

(214) Step 5: turning on the physical vapor deposition device to deposit the high-melting particles onto the dispersed NdFeB magnetic powder by the physical vapor deposition;

(215) The physical vapor deposition includes magnetron sputtering deposition, ion plating deposition, and evaporation source deposition. The deposition rate of the high-melting particles is 0.01-50 μm/min. The high-melting particles are particles of elements W, Mo, V, Ti, Ta, Zr, Nb, Co, Cr or Ga.

(216) Step 6: terminating the physical vapor deposition, and taking out the NdFeB magnetic powder after its temperature decreases to room temperature;

Example 17

(217) (1) Ingredients-mixing, smelting, strip casting, disc crushing and ball milling were performed, so as to obtain a NdFeB magnetic powder with an average particle size of 3.5 μm;

(218) (2) Physical vapor deposition was carried out to cover the obtained magnetic powder.

(219) Ti metal target material was selected, the chamber was evacuated to a vacuum degree of 2.0×10.sup.−2 Pa, argon was charged to 0.2 Pa; the magnetic powder was heated to 380° C., magnetron sputtering was carried out with the sputtering power adjusted to get Ti particle deposition rate of 0.01 μm/min, and the covered NdFeB magnetic powder was taken out after its temperature decreases to room temperature.

(220) Orientation molding, sintering and heat treatment were performed on the obtained magnetic powder, so as to obtain a final NdFeB magnet. The magnetic energy product and the coercive force of the magnet prepared in this example were tested with a magnetic property measuring instruments, and compared with the magnet prepared with the same addition amount of Ti by the conventional method. The results are shown in Table 17.

(221) TABLE-US-00017 TABLE 17 Intrinsic coercive Maximum magnetic Remanence/ force/ energy product/ Samples kGs kOe MGOe Conventional 12.62 18.39 37.51 method Covering 12.55 20.83 38.40 method

Example 18

(222) (1) Ingredients-mixing, smelting, strip casting, hydrogen crushing and jet milling were performed, so as to obtain NdFeB magnetic powder with an average particle size of 4.1 μm;

(223) (2) Physical vapor deposition was carried out to cover the obtained magnetic powder.

(224) Mo metal target material was selected, the chamber was evacuated to a vacuum degree of 5.0×10.sup.−3 Pa, argon was charged to 0.5 Pa; the magnetic powder was heated to 420° C., magnetron sputtering was carried out with the sputtering power adjusted to get Mo particle deposition rate of 50 μm/min, and the covered NdFeB magnetic powder was taken out after its temperature decreases to room temperature.

(225) Orientation molding, sintering and heat treatment were performed on the obtained magnetic powder, so as to obtain a final NdFeB magnet. The magnetic energy product and the coercive force of the magnet prepared in this example were tested with a magnetic property measuring instruments, and compared with the magnet prepared with the same addition amount of Mo by the conventional method. The results are shown in Table 18.

(226) TABLE-US-00018 TABLE 18 Intrinsic coercive Maximum magnetic Remanence/ force/ energy product/ Samples kGs kOe MGOe Conventional 13.48 19.36 42.97 method Covering 13.13 22.45 43.62 method

Example 19

(227) (1) Ingredients-mixing, smelting, strip casting, hydrogen crushing were performed, so as to obtain NdFeB magnetic powder;

(228) (2) Physical vapor deposition was carried out to cover the obtained magnetic powder;

(229) CoZr metal target material was selected, the chamber was evacuated to a vacuum degree of 9.0×10.sup.−4 Pa, the magnetic powder was heated to 300° C., the vapor deposition was carried out with the heating source power of the evaporation boat adjusted to get CoZr atoms vaporized and evaporated at a deposition rate of 3 μm/min, and the covered NdFeB magnetic powder was taken out after its temperature decreases to room temperature.

(230) (3) Jet milling was performed on the obtained magnetic powder, so as to prepare NdFeB magnetic powder with an average particle size of 3.7 μm.

(231) Orientation molding, sintering and heat treatment were performed on the prepared NdFeB magnetic powder, so as to obtain a final NdFeB magnet. The magnetic energy product and the coercive force of the magnet prepared in this example were tested with a magnetic property measuring instruments, and compared with the magnet prepared with the same addition amount of CoZr by the conventional method. The results are shown in Table 19.

(232) TABLE-US-00019 TABLE 19 Intrinsic coercive Maximum magnetic Remanence/ force/ energy product/ Samples kGs kOe MGOe Conventional 13.18 19.80 41.75 method Covering 12.97 23.38 42.30 method

(233) Scheme 6:

(234) A method for preparing NdFeB magnetic powder using a heavy rare earth, comprising the specific steps as follows:

(235) Step 1: preparing NdFeB magnetic powder of 1 μm-2 mm;

(236) After smelting and casting, the NdFeB magnet is mechanically crushed, or hydrogen crushed, or crushed in an air jet mill to prepare NdFeB magnetic powder.

(237) Step 2: selecting a desired heavy rare earth target material; placing the NdFeB magnetic powder and the heavy rare earth target material in a physical vapor deposition device, respectively;

(238) The heavy rare earth target material is at least one selected from the group of pure metal, alloy or oxide of Dy, Tb or Dy-Tb.

(239) Step 3: evacuating the chamber to a degree of vacuum lower than 2.0×10.sup.−2 Pa, charging argon to 0.2-1.0 Pa;

(240) Step 4: adjusting the parameters to uniformly disperse the NdFeB magnetic powder while heating the NdFeB magnetic powder, where the heating temperature is 300-500° C.;

(241) Step 5: turning on the physical vapor deposition device to deposit the heavy rare earth particles onto the dispersed NdFeB magnetic powder by the physical vapor deposition;

(242) The physical vapor deposition includes magnetron sputtering deposition, ion plating deposition, and evaporation source deposition. The heavy rare earth particle deposition rate is 0.01-50 μm/min.

(243) Step 6: terminating the physical vapor deposition, and taking out the NdFeB magnetic powder after its temperature decreases to room temperature.

Example 20

(244) (1) Ingredients-mixing, smelting, strip casting, disc crushing and ball milling were performed, so as to obtain NdFeB magnetic powder with an average particle size of 3.5 μm;

(245) (2) Physical vapor deposition was carried out to cover the obtained magnetic powder.

(246) Dy metal target material was selected, the chamber was evacuated to a vacuum degree of 2.0×10.sup.−2 Pa, argon was charged to 0.2 Pa; the magnetic powder was heated to 380° C.; magnetron sputtering was carried out with the sputtering power adjusted to get Dy particle deposition rate of 0.01 μm/min, and the covered NdFeB magnetic powder was taken out after its temperature decreases to room temperature.

(247) (3) Orientation molding, sintering and heat treatment were performed on the obtained magnetic powder, so as to obtain a final NdFeB magnet.

(248) The magnetic energy product and the coercive force of the magnet prepared in this example were tested with a magnetic property measuring instruments, and compared with the magnet prepared by the conventional method. The results are shown in Table 20.

(249) TABLE-US-00020 TABLE 20 Intrinsic coercive Maximum magnetic Remanence/ force/ energy product/ Samples kGs kOe MGOe NdFeB 12.62 18.39 37.51 NdFeB—Dy 12.55 22.83 37.80

Example 21

(250) (1) Ingredients-mixing, smelting, strip casting, hydrogen crushing and jet milling were performed, so as to obtain NdFeB magnetic powder with an average particle size of 4.1 μm;

(251) (2) Physical vapor deposition was carried out to cover the obtained magnetic powder;

(252) Tb metal target material was selected, the chamber was evacuated to a vacuum degree of 5.0×10.sup.−3 Pa, argon was charged to 0.5 Pa; the magnetic powder was heated to 420° C., ion plating (the atoms from the target are mostly in an ion state with a higher energy, leading to a better combination with the surface of the NdFeB magnetic powder) was performed. The current of the argon source was adjusted so that the deposition rate of the Tb particles was 50 μm/min, and the covered NdFeB magnetic powder was taken out after its temperature decreases to room temperature.

(253) (3) Orientation molding, sintering and heat treatment were performed on the obtained magnetic powder, so as to obtain a final NdFeB magnet.

(254) The magnetic energy product and the coercive force of the magnet prepared in this example were tested with a magnetic property measuring instruments, and compared with the magnet prepared by the conventional method. The results are shown in Table 21.

(255) TABLE-US-00021 TABLE 21 Intrinsic coercive Maximum magnetic Remanence/ force/ energy product/ Samples kGs kOe MGOe NdFeB 13.48 19.36 42.97 NdFeB—Tb 13.13 28.45 41.62

Example 22

(256) (1) Ingredients-mixing, smelting, strip casting, hydrogen crushing were performed, so as to obtain NdFeB magnetic powder;

(257) (2) Physical vapor deposition was carried out to cover the obtained magnetic powder;

(258) DyTb metal target material was selected, the chamber was evacuated to a vacuum degree of 9.0×10.sup.−4 Pa, the magnetic powder was heated to 300° C., the vapor deposition was carried out with the heating source power of the evaporation boat adjusted to get DyTb atoms vaporized and evaporated at a deposition rate of 3 μm/min, and the covered NdFeB magnetic powder was taken out after its temperature decreases to room temperature.

(259) (3) Jet milling was performed on the obtained magnetic powder, so as to prepare NdFeB magnetic powder with an average particle size of 3.7 μm;

(260) (4) Orientation molding, sintering and heat treatment were performed on the prepared NdFeB magnetic powder, so as to obtain a final NdFeB magnet.

(261) The magnetic energy product and the coercive force of the magnet prepared in this example were tested with a magnetic property measuring instruments, and compared with the magnet prepared by the conventional method. The results are shown in Table 22.

(262) TABLE-US-00022 TABLE 22 Intrinsic coercive Maximum magnetic Remanence/ force/ energy product/ Samples kGs kOe MGOe NdFeB 13.18 19.80 41.75 NdFeB—DyTb 12.97 26.38 40.70

Example 23

(263) (1) Ingredients-mixing, smelting, strip casting, hydrogen crushing and jet milling were performed, so as to obtain magnetic powder of NdFeB alloy with an average particle size of 4.3 μm;

(264) (2) Physical vapor deposition was carried out to cover the obtained magnetic powder;

(265) Dy.sub.2O.sub.3 target material was selected, the chamber was evacuated to a vacuum degree of 3.0×10.sup.−2 Pa, argon was charged to 0.3 Pa, the magnetic powder was heated to 500° C., magnetron sputtering was performed with the sputtering power adjusted to get Dy.sub.2O.sub.3 particle deposition rate of 0.2 μm/min, and the covered NdFeB magnetic powder was taken out after its temperature decreases to room temperature.

(266) (3) Orientation molding, sintering and heat treatment were performed on the magnetic powder obtained in the step (2), so as to obtain a final NdFeB magnet.

(267) The magnetic energy product and the coercive force of the magnet prepared in this example were tested with a magnetic property measuring instruments, and compared with the magnet prepared by the conventional method. The results are shown in Table 23.

(268) TABLE-US-00023 TABLE 23 Intrinsic coercive Maximum magnetic Remanence/ force/ energy product/ Samples kGs kOe MGOe NdFeB 13.32 19.43 42.13 NdFeB—Dy.sub.2O.sub.3 13.18 23.59 41.65

(269) Scheme 7:

(270) A method for preparing an NdFeB magnet with a low amount of heavy rare earth but high coercive force, comprising the specific steps as follows:

(271) Step 1: mixing the ingredients according to the formula, smelting and strip casting the mixture;

(272) Step 2: hydrogen crushing, disproportionation reaction, and jet milling are carried out on NdFeB cast sheets to obtain NdFeB fine powder, which has an average particle diameter D.sub.50 of 300 nm-20 μm;

(273) Step 3: heavy rare earth element particles and high-melting element particles are deposited onto the NdFeB fine powder by thermal resistance evaporation deposition;

(274) The heavy rare earth element particles are particles of elements Dy or Tb, and the high-melting element particles are particles of elements W, Mo, V, Ti, Ta, Zr, Nb, Co, Cr or Ga.

(275) In the thermal resistance evaporation deposition process, the NdFeB fine powder and the heavy rare earth thermal resistance wire are respectively placed in the thermal resistance evaporation deposition device, and the vacuum degree of thermal resistance evaporation is 10.sup.5 Pa-10.sup.2 Pa; adjusting the parameters so as to uniformly disperse the NdFeB fine powder; evaporating the heavy rare earth element particles by heating the heavy rare earth thermal resistance wire, so that the heavy rare earth element particles may be deposited on the NdFeB fine powder; taking out the NdFeB fine powder after its temperature decreased to room temperature. For the heavy rare earth thermal resistance wire, the heavy rare earth element is pure metal or alloy of at least one element selected from Dy or Tb.

(276) In the thermal resistance evaporation deposition process, the NdFeB fine powder and the high-melting thermal resistance wire are placed in the thermal resistance evaporation deposition device, and the vacuum degree of thermal resistance evaporation is 10.sup.5 Pa-10.sup.2 Pa; adjusting the parameters so as to uniformly disperse the NdFeB fine powder; evaporating the high-melting element particles by heating the high-melting thermal resistance wire, so that the high-melting element particles may be deposited on the NdFeB fine powder; taking out the NdFeB fine powder after its temperature decreased to room temperature. The high-melting thermal resistance wire is pure metal or alloy of at least one element selected from elements W, Mo, V, Ti, Ta, Zr, Nb, Co, Cr or Ga.

(277) Step 4: performing orientation compression molding, sintering in vacuum and heat treatment on the obtained NdFeB fine powder, so as to obtain a final NdFeB magnet.

Example 24

(278) (1) Ingredients-mixing, smelting, strip casting were performed, so as to obtain NdFeB cast sheet;

(279) (2) Hydrogen crushing, disproportionation reaction, and jet milling were carried out to obtain NdFeB fine powder with an average particle diameter D.sub.50 of 400 nm;

(280) (3) The NdFeB fine powder and the Dy thermal resistance wire were respectively placed in the thermal resistance evaporation deposition device; the vacuum degree was 10.sup.3 Pa; the parameters were set so as to uniformly disperse the NdFeB fine powder; the thermal resistance wire was heated to evaporate and deposit the Dy particles on the NdFeB fine powder; the NdFeB fine powder was taken out after its temperature decreased to room temperature.

(281) (4) Orientation molding, sintering and heat treatment were performed on the obtained NdFeB fine powder, so as to obtain a final NdFeB magnet. The magnetic energy product and the coercive force of the magnet prepared in this example were tested with a magnetic property measuring instruments, and compared with the magnet prepared by the conventional method. The results are shown in Table 24.

(282) TABLE-US-00024 TABLE 24 Intrinsic coercive Maximum magnetic Remanence/ force/ energy product/ Samples kGs kOe MGOe NdFeB 12.62 18.39 37.51 NdFeB—Dy 12.55 22.83 increased

Example 25

(283) (1) Ingredients-mixing, smelting, strip casting were performed, so as to obtain NdFeB cast sheet;

(284) (2) Hydrogen crushing, disproportionation reaction, and jet milling were carried out to obtain NdFeB fine powder with an average particle diameter D.sub.50 of 800 nm;

(285) (3) The NdFeB fine powder and the Tb thermal resistance wire were respectively placed in the thermal resistance evaporation deposition device; the vacuum degree was 10.sup.3 Pa; the parameters were set so as to uniformly disperse the NdFeB fine powder; the thermal resistance wire was heated to evaporate and deposit the Tb particles on the NdFeB fine powder; the NdFeB fine powder was taken out after its temperature decreased to room temperature.

(286) (4) Orientation molding, sintering and heat treatment were performed on the obtained NdFeB fine powder, so as to obtain a final NdFeB magnet. The magnetic energy product and the coercive force of the magnet prepared in this example were tested with a magnetic property measuring instruments, and compared with the magnet prepared by the conventional method. The results are shown in Table 25.

(287) TABLE-US-00025 TABLE 25 Intrinsic coercive Maximum magnetic Samples Remanence/kGs force/kOe energy product/MGOe NdFeB 13.48 19.36 42.97 NdFeB—Tb 13.13 28.45 increased

Example 26

(288) (1) Ingredients-mixing, smelting, strip casting were performed, so as to obtain NdFeB cast sheet;

(289) (2) Hydrogen crushing, disproportionation reaction, and jet milling were carried out to obtain NdFeB fine powder with an average particle diameter D.sub.50 of 1 μm;

(290) (3) The NdFeB fine powder and the CoZr thermal resistance wire were respectively placed in the thermal resistance evaporation deposition device; the vacuum degree was 10.sup.3 Pa; the parameters were set so as to uniformly disperse the NdFeB fine powder; the thermal resistance wire was heated to evaporate and deposit the CoZr particles on the NdFeB fine powder; the NdFeB fine powder was taken out after its temperature decreased to room temperature.

(291) (4) Orientation molding, sintering and heat treatment were performed on the obtained NdFeB fine powder, so as to obtain a final NdFeB magnet. The magnetic energy product and the coercive force of the magnet prepared in this example were tested with a magnetic property measuring instruments, and compared with the magnet prepared by the conventional method. The results are shown in Table 26.

(292) TABLE-US-00026 TABLE 26 Intrinsic coercive Maximum magnetic Remanence/ force/ energy product/ Samples kGs kOe MGOe NdFeB 13.18 19.80 41.75 NdFeB—CoZr 12.97 23.38 increased

(293) Scheme 8:

(294) A method for preparing NdFeB fine powder, comprising the specific steps as follows:

(295) Step 1: mixing the ingredients according to the formula, smelting and strip casting the mixture;

(296) Step 2: hydrogen crushing, disproportionation reaction, and jet milling are carried out on NdFeB cast sheets to obtain NdFeB fine powder, which has an average particle diameter D.sub.50 of 300 nm-20 μm;

(297) Step 3: heavy rare earth element particles and high-melting element particles are deposited onto the NdFeB fine powder by thermal resistance evaporation deposition;

(298) The high-melting particles are particles of elements W, Mo, V, Ti, Ta, Zr, Nb, Co, Cr or Ga; and the heavy rare earth element particles are particles of elements Dy or Tb.

(299) In the thermal resistance evaporation deposition process, the NdFeB fine powder and the heavy rare earth thermal resistance wire are respectively placed in the thermal resistance evaporation deposition device, and the vacuum degree of thermal resistance evaporation is 10.sup.5 Pa-10.sup.2 Pa; adjusting the parameters so as to uniformly disperse the NdFeB fine powder; evaporating the heavy rare earth element particles by heating the heavy rare earth thermal resistance wire, so that the heavy rare earth element particles may be deposited on the NdFeB fine powder; taking out the NdFeB fine powder after its temperature decreased to room temperature. For the heavy rare earth thermal resistance wire, the heavy rare earth element is pure metal or alloy of at least one element selected from Dy or Tb.

(300) In the thermal resistance evaporation deposition process, the NdFeB fine powder and the high-melting thermal resistance wire are respectively placed in the thermal resistance evaporation deposition device, and the vacuum degree of thermal resistance evaporation is 10.sup.5 Pa-10.sup.2 Pa; adjusting the parameters so as to uniformly disperse the NdFeB fine powder; evaporating the high-melting particles by heating the high-melting thermal resistance wire, so that the high-melting element particles may be deposited on the NdFeB fine powder; taking out the NdFeB fine powder after its temperature decreased to room temperature. The high-melting thermal resistance wire is pure metal or alloy of at least one element selected from element W, Mo, V, Ti, Ta, Zr, Nb, Co, Cr or Ga.

(301) Step 4: taking out the NdFeB fine powder after its temperature decreased to room temperature.

Example 27

(302) (1) Ingredients-mixing, smelting, strip casting, hydrogen crushing, disproportionation reaction, and jet milling were carried out to obtain NdFeB fine powder with an average particle diameter D.sub.50 of 400 nm;

(303) (2) The NdFeB fine powder and the DyTb thermal resistance wire were respectively placed in the thermal resistance evaporation deposition device; the vacuum degree was 10.sup.3 Pa; the parameters were set so as to uniformly disperse the NdFeB fine powder; the thermal resistance wire was heated to evaporate and deposit the Dy or Tb particles on the NdFeB fine powder; the covered NdFeB fine powder was taken out after its temperature decreased to room temperature.

(304) (3) Orientation molding, sintering and heat treatment were performed on the obtained NdFeB fine powder, so as to obtain a final NdFeB magnet. The magnetic energy product and the coercive force of the magnet prepared in this example were tested with a magnetic property measuring instruments, and compared with the magnet prepared by the conventional method. The results are shown in Table 27.

(305) TABLE-US-00027 TABLE 27 Intrinsic coercive Maximum magnetic Remanence/ force/ energy product/ Samples kGs kOe MGOe Conventional 12.62 18.39 37.51 method Covering 12.55 22.83 increased method

Example 28

(306) (1) Ingredients-mixing, smelting, strip casting, hydrogen crushing, disproportionation reaction, and jet milling were carried out to obtain NdFeB fine powder with an average particle diameter D.sub.50 of 800 nm;

(307) (2) The NdFeB fine powder and the Tb thermal resistance wire were respectively placed in the thermal resistance evaporation deposition device; the vacuum degree was 10.sup.3 Pa; the parameters were set so as to uniformly disperse the NdFeB fine powder; the thermal resistance wire was heated to evaporate and deposit the Tb particles on the NdFeB fine powder; the covered NdFeB fine powder was taken out after its temperature decreased to room temperature.

(308) (3) Orientation molding, sintering and heat treatment were performed on the obtained NdFeB fine powder, so as to obtain a final NdFeB magnet. The magnetic energy product and the coercive force of the magnet prepared in this example were tested with a magnetic property measuring instruments, and compared with the magnet prepared with the same addition amount of Tb by the conventional method. The results are shown in Table 28.

(309) TABLE-US-00028 TABLE 28 Intrinsic coercive Maximum magnetic Remanence/ force/ energy product/ Samples kGs kOe MGOe Conventional 13.48 19.36 42.97 method Covering 13.13 28.45 increased method

Example 29

(310) (1) Ingredients-mixing, smelting, strip casting, hydrogen crushing, disproportionation reaction, and jet milling were carried out to obtain NdFeB fine powder with an average particle diameter D.sub.50 of 1 μm;

(311) (2) The NdFeB fine powder and the CoZr thermal resistance wire were respectively placed in the thermal resistance evaporation deposition device; the vacuum degree was 10.sup.3 Pa; the parameters were set so as to uniformly disperse the NdFeB fine powder; the thermal resistance wire was heated to evaporate and deposit the CoZr particles on the NdFeB fine powder; the covered NdFeB fine powder was taken out after its temperature decreased to room temperature.

(312) (3) Orientation molding, sintering and heat treatment were performed on the obtained NdFeB fine powder, so as to obtain a final NdFeB magnet. The magnetic energy product and the coercive force of the magnet prepared in this example were tested with a magnetic property measuring instruments, and compared with the magnet prepared with the same addition amount of CoZr by the conventional method. The results are shown in Table 29.

(313) TABLE-US-00029 TABLE 29 Intrinsic coercive Maximum magnetic Remanence/ force/ energy product/ Samples kGs kOe MGOe Conventional 13.18 19.80 41.75 method Covering 12.97 23.38 increased method

(314) The terms used in this disclosure are illustrative and exemplary, thus should not be construed as limitation. The present invention may be implemented in a variety of forms without departing from the spirit or scope of the invention. Thus, it should be understood that the above examples are not limited to the aforementioned details, but should be generally explained in the spirit and scope defined by the accompanied claims. Therefore, all changes and modifications that fall within the scope of the claims or the equivalents thereof are intended to be covered by the appended claims.

INDUSTRIAL APPLICABILITY

(315) The heavy rare earth particles or the high-melting particles are uniformly dispersed at the grain boundaries in the magnet, that increases the coercive force of the magnet, refines the crystal grains of the magnet, and reduces the usage amount of heavy rare earth; the coercive force of the NdFeB magnet is significantly increased, the amount of heavy rare earth element is greatly reduced, the manufacturing cost of the NdFeB magnet is decreased, and the oxygen content in the magnet is reduced.