BACKGROUND OF THE INVENTION
[0001] Flexible permanent magnets have been used extensively in gasket assemblies for sealing
the space between the door and cabinet of refrigerators, food freezers and like structures.
Such magnets also have found extensive use in a variety of other applications, including
use in advertising sheet materials that can be removably attached to an appropriate
metal surface, as an attaching component in storm window framing, in motors, in sheet
backing for carpeting to anchor the carpeting to steel flooring, as toy components,
etc.
[0002] As described in U.S. Patent No. 2,959,832, such magnets may be made by incorporating
a magnetic powder into an elastomer binder and shaping the composition into the desired
configuration, followed by orientation of the particles of magnetic powder within
the binder in order to enhance the potential magnetic properties of the composition.
The resulting composition is subjected to a magnetizing field to magnetize the particles
of magnetic powder within the composition.
[0003] The mixing operation can be carried out in any convenient manner, such as by mixing
the components of the magnetic composition together in a Banbury mixer, on a roll
mill or in an extruder. The method or methods which can be used for shaping the composition
will depend to a significant degree on the configuration into which the composition
is to be formed. For example, if thin sheets of the magnetic composition are desired,
the sheets can be formed by a conventional calendering operation. Strip magnets of
the type used in refrigerator gasket assemblies normally are formed as a continuous
strip by extruding the magnetic composition through an appropriately-shaped extrusion
die. Magnetization of the particles of magnetic material within the composition can
be accomplished by subjecting the shaped product to a magnetic field of sufficient
strength.
[0004] The amount of powdered magnetic material present in the magnetic composition will
influence the strength of a magnet that can be formed from the composition. Usually,
the larger the quantity of powered magnetic material in the composition, the greater
will be the strength of a magnet which can be formed from the composition (provided
that the degree of orientation of the magnetic particles is equal). However, as the
quantity of powdered magnetic material in the composition is increased, the stiffness
of the composition also increases and ultimately the composition may become friable
and unable to be "worked" further. Also, the energy required for mixing or the pressure
required for extrusion may become objectionably high as greater quantities of the
magnetic powder are added to the composition.
SUMMARY OF THE INVENTION
[0005] The present invention provides a magnetic composition that exhibits outstanding processing
characteristics that enable the composition to be processed easily using less energy
input and to be extruded at extrusion pressures lower than required with current commercial
compositions containing comparable loadings of magnetic material The composition is
able to accommodate higher loadings of the powdered magnetic material without losing
its capability of being "worked" and shaped and, as a result of the possible higher
loadings, can be formed into magnets of higher strengths.
[0006] In accordance with the present invention, a magnetic composition is provided that
is comprised of (1) powdered magnetic material and (2) a polyacrylic elastomer binder
for the magnetic material. Magnets formed from the composition not only can be of
higher strength due to the higher loadings of magnetic powder that can be included
in the composition, but also can be made into magnets that have a greater degree of
flexibility than previously realized and which will withstand higher temperatures
without exhibiting objectionable degradation.
DETAILED DESCRIPTION OF THE INVENTION
[0007] As indicated above, the magnetic composition of the present invention is comprised
of (1) a finely-divided magnetic material and (2) polyacrylic elastomer binder for
the magnetic material. The magnetic material can be combined with the polyacrylic
elastomer component of the composition in any convenient manner, such as by mixing
the components of the composition together in a Banbury mixer or on a roll mill. The
mixed composition, usually is cubed or granulated to put it in a form that can be
handled easily for further processing. The composition then is shaped into the desired
configuration. If a flat thin sheet is desired, shaping can be accomplished on a calendering
mill. If a magnet in the form of a strip is required, the cubed or granulated magnetic
composition can be fed into a screw-type extruder and forced through an appropriately-shaped
extrusion die to form a continuous strip of the magnetic composition of the desired
cross-sectional configuration. The composition also can be shaped by injection molding
or by shaping in conventional sectional molds. The shaped composition thereafter is
exposed to a magnetizing field to magnetize the magnetic particles with the composition.
[0008] The binder component of the composition can be any polyacrylic elastomer that has
a Mooney viscosity between 20 to 70, preferably between 25 to 60, when measured according
to the procedure described in ASTM Designation No. 1646 after four minutes running
time at 100°C. using the large rotor and with a one minute warm-up period and that
is a polymer comprised of from 95 to 100 percent by weight of a backbone component
having the structure:

derived from an alkyl acrylate (such as ethyl acrylate, propyl acrylate, n-butyl acrylate,
hexyl acrylate, heptyl acrylate and octyl acrylate) and where x is an integer and
n is from 2 to 8, or having the structure

derived from an alkoxy acrylate (such as methoxy ethyl acrylate and ethoxy ethyl acrylate)
and where x is an integer, n is 2 and m is 1 or 2. The polymer may contain up to 5
percent by weight of reactive functional groups that can function as cure cites. Among
the reactive functional groups are reactive halogen groups having the structure

where X is chlorine or bromine (such as results from the copolymerization of the alkyl
acrylate or alkoxy acrylate with 2-chlorethyl vinyl ether), or reactive epoxy groups
having the structure

(such as results from the copolymerization of the alkyl acrylate or alkoxy acrylate
with an alkyl glycidyl ether), or reactive carboxyl groups having the structure

(such as results from the copolymerization of the alkyl acrylate or alkoxy acrylate
with acrylic acid or methacrylic acid) or reactive hydroxyl groups having the structure

(such as results from the copolymerization of the alkyl acrylate or alkoxy acrylate
with an hydroxalkyl acrylate).
[0009] The magnetic component can be any anisotropic magnetizable material in fine particulate
form, but preferably is a ferrite of barium, lead, or strontium, or a mixture thereof
in a finely-divided state so that the individual particles desirably approach the
size of the magnetic domains of the material. As used herein, a ferrite is defined
as a material having the formula MO.nFe
20
3 wherein M is barium, lead or strontium and n is an integer. Of the commercial ferrites,
barium ferrite (BaFe
120
19) is preferred. The particle size of the magnetic component desirably is within the
size range of 0.5 to 10 microns with an average particle size preferably being 1 to
1.5 microns. Although commercial flexible permanent magnets currently being sold can
contain as an upper limit only about 1,000 parts by weight of the magnetic component
per 100 parts by weight of the binder component (since use of more than about 1000
parts by weight of the magnetic component per 100 parts by weight of binder produces
a composition that is unable to be worked satisfactorily and that is objectionably
friable and brittle), the composition of the present invention can accommodate up
to about 1200 parts by weight of the magnetic material per 100 parts by weight of
the polyacrylic binder component. As a result of the increased amount of magnetic
material that can be incorporated into the composition, magnets of greater magnetic
strength can be formed.
[0010] If desired, a small quantity of a processing aid for the polyacrylic binder component
can be added to the composition. The processing aid should have a softening point
below the temperature at which the magnetic composition is mixed and shaped to produce
optimum results. Polyethylene homopolymers and copolymers of ethylene with an acrylic
acid or vinyl acetate which have softening points when measured in accordance with
the procedure described in ASTM Designation No. E-28 of between 60 to 120°C. are preferred
processing aids. Desirably, from 1 to 15 parts by weight of such processing aid is
used per 100 parts by weight of the polyacrylic elastomer in the magnetic composition.
[0011] The invention will be further understood by reference to the following examples.
EXAMPLES I-V
[0012] Magnetic compositions were formed having the following compositions:

[0013] The ingredients were mixed together on a roll mill, sheeted off the mill and granulated.
The granules were fed to a conventional extruder fitted with a heated die which produced
a strip-type extrusion rectangular in cross-section. As the strip of material was
discharged from the extrusion die, it was advanced through a magnetic field to magnetize
the particles of ferrite in the composition. Various operating conditions employed
in the manufacture of the strip materials and selected physical properties of the
strip magnet formed are listed in Table I:

[0014] A typical commercial magnetic composition having the following composition served
as a "control" was formed into a strip magnet as described in Examples I-V:

[0015] The "control" strip magnet had the following physical properties:
PROPERTIES OF CONTROL
[0016]

The invention is further illustrated by the following examples.
EXAMPLES VI-XIII
[0017] Magnetic compositions were formed using the following formulation:

[0018] The polymer binders used in the examples were:

[0019] The compositions were mixed on an open mill. Mixing time for the polyacrylic elastomer
binder compositions (Examples VI-X) was ten (10) minutes and mixing time for the chlorosulfonated
polyethylene/polyisobutylene binder compositions was 20 minutes. Each composition
was run through a capillary extrusion die in a constant load rheometer at the following
conditions:

[0020] The data obtained is tabulated in Table II.

1. A flexible permanent magnet composition comprising
a. finely-divided particles of a ferrite having the formula MO.nFe202 in which M is barium, lead or strontium and n is an integer, and
b. a polyacrylic elastomer having a Mooney viscosity between 20 and 70 when measured
in accordance with the procedure of ASTM Designation 1646 with a 4 minute running
time at 100°C. using the large rotor and with a 1 minute warm-up period,
said polyacrylic elastomer being a polymer comprised of from 95 to 100 percent by
weight of a backbone component having the structure

derived from an alkyl acrylate, where x is an integer and n is from 2 to 8, or having
the structure

derived from an alkyoxy acrylate, where x in an integer, n is 2 and m is 1 or 2, said
ferrite being present in an amount up to about 1200 parts by weight of said ferrite
per 100 parts by weight of said polyacrylic elastomer.
2. The composition of claim 1 wherein said polyacrylic elastomer polymer contains
up to 5 percent by weight of reactive functional groups.
3. The composition of claim 2 wherein said reactive functional groups are reactive
halogen groups having the structure

where X is chlorine or bromine.
4. The composition of claim 2 wherein said reactive functional groups are reactive
epoxy groups having the structure
5. The composition of claim 2 wherein said reactive functional groups are reactive
carboxyl groups having the structure
6. The composition of claim 2 wherein said reactive functional groups are reactive
hydroxyl groups having the structure
7. The composition of claim 1 wherein said polyacrylic elastomer has a Mooney viscosity
between 25 to 60 when measured in accordance with the procedure of ASTM Designation
1646 with a 4 minute running time at 100°C. using the large rotor and with a 1 minute
warm-up period.
8. The composition of claim 1 wherein said finely-divided particles of ferrite have
a particle size within the range of from 0.5 to 10 microns and an average particle
size from 1 to 1.5 microns.
9. The composition of claims 1, 2, 3, 4, 5, 6, 7 or 8 wherein said ferrite is barium
ferrite (BaFe12O19).
10. The composition of claims 1, 2, 3, 4, 5, 6, or 7 wherein said composition contains
from 1 to 15 parts by weight of a polyethylene homopolymer or a copolymer of ethylene
with an acrylic acid or vinyl acetate per 100 parts by weight of said polyacrylic
elastomer.