Method for manufacturing a magnetic powder for high density magnetic recording

Claim 1

A method for manufacturing a magnetic powder for high density magnetic recording, comprising: mixing, together with boron trioxide as a glass forming substance metal oxide or metal oxide precursor components including A oxide or A oxide precursor, iron oxide or iron oxide precursor, cobalt oxide or cobalt oxide precursor, and M oxide or M oxide precursor of a substituted ferrite having the formula: AFe.sub.12-2x Co.sub.x M.sub.x O.sub.19 or Afe.sub.12-3/2x Co.sub.x M.sub.1/2x O.sub.19 wherein A is at least one element selected from the group consisting of barium, strontium, lead and calcium, M is at least one tetravalent element selected from the group consisting of titanium and germanium or at least one pentavalent element selected from the group consisting of vanadium, niobium, anitmony and tantalum, and x is a value from 0.5 to 1.1, in amounts within a triangular area whose verteces are a point (a) defined by B 2 O 3 =0 mol %, the A oxide or A oxide precursor=14.3 mol %, and a total of the iron oxide or iron oxide precursor plus the coblat oxide or cobalt oxide precursor plus the M oxide or M oxide precursor=85.7 mol %, a point (b) defined by B 2 O 3 =0 mol %, the A oxide or A oxide precursor=16.7 mol %, and a total of the iron oxide or iron oxide precursor plus the cobalt oxide or cobalt oxide precursor plus the M oxide or M oxide precursor=83.8 mol %, and a point (c) defined by B 2 O 3 =50 mol %, the A oxide or A oxide precursor=50 mol %, and a total of the iron oxide or iron oxide precursor plus the cobalt oxide or cobalt oxide precursor plus the M oxide or M oxide precursor=0 mol %, as described by the triangular area (b) (c) (a) of FIG. 2; (excluding the line connecting the points (a) and (b)) melting the mixture into a molten material; rapidly cooling the molten material to obtain an amorphous material; heat-treating the amorphous material to precipitate a substituted hexogonal ferrite as mutually separated fine particles in a glass matrix; and separating out the fine particles from the glass matrix.

Claim 2

A method for manufacturing a magnetic powder for high density magnetic recording, comprising: mixing, together with boron trioxide as a glass forming substance metal oxide or metal oxide precursor components including A oxide or A oxide precursor, iron oxide or iron oxide precursor, cobalt oxide or cobalt oxide precursor, and M oxide or M oxide precursor of a substituted ferrite having the formula: AFe.sub.12-2x Co.sub.x M.sub.x O.sub.19 or Afe.sub.12-3/2x Co.sub.x M.sub.1/2x O.sub.19 wherein A is at least one element selected from the group consisting of barium, strontium, lead and calcium, M is at least one tetravalent element selected from the group consisting of titanium and germanium or at least one pentavalent element selected from the group consisting of vanadium, niobium, anitmony and tantalum, and x is a value from 0.5 to 1.1, in amounts within a triangular area whose verteces are a point (a) defined by B 2 O 3 =0 mol %, the A oxide or A oxide precursor=14.3 mol %, and a total of the iron oxide or iron oxide precursor plus the coblat oxide or cobalt oxide precursor plus the M oxide or M oxide precursor=85.7 mol %, a point (b) defined by B 2 O 3 =0 mol %, the A oxide or A oxide precursor=16.7 mol %, and a total of the iron oxide or iron oxide precursor plus the cobalt oxide or cobalt oxide precursor plus the M oxide or M oxide precursor=83.8 mol %, and a point (c) defined by B 2 O 3 =50 mol %, the A oxide or A oxide precursor=50 mol %, and a total of the iron oxide or iron oxide precursor plus the cobalt oxide or cobalt oxide precursor plus the M oxide or M oxide precursor=0 mol %, as described by the triangular area (b) (c) (a) of FIG. 2; (excluding the line connecting the points (a) and (b)) melting the mixture into a molten material; rapidly cooling the molten material to obtain an amorphous material; heat-treating the amorphous material to precipitate a substituted hexogonal ferrite as mutually separated fine particles in a glass matrix; and separating out the fine particles from the glass matrix.

Claim 9

The method as claimed in any one of claims 1 to 7, wherein the heat treatment is performed at 700° to 850° C. for 2 hours or more.