GB2035344A - Magnetodielectric material - Google Patents
Magnetodielectric material Download PDFInfo
- Publication number
- GB2035344A GB2035344A GB7835272A GB7835272A GB2035344A GB 2035344 A GB2035344 A GB 2035344A GB 7835272 A GB7835272 A GB 7835272A GB 7835272 A GB7835272 A GB 7835272A GB 2035344 A GB2035344 A GB 2035344A
- Authority
- GB
- United Kingdom
- Prior art keywords
- weight
- phenol formaldehyde
- lubricant
- resin
- process according
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
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Classifications
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L61/00—Compositions of condensation polymers of aldehydes or ketones; Compositions of derivatives of such polymers
- C08L61/04—Condensation polymers of aldehydes or ketones with phenols only
- C08L61/06—Condensation polymers of aldehydes or ketones with phenols only of aldehydes with phenols
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B3/00—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties
- H01B3/02—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of inorganic substances
- H01B3/06—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of inorganic substances asbestos
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B3/00—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties
- H01B3/02—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of inorganic substances
- H01B3/08—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of inorganic substances quartz; glass; glass wool; slag wool; vitreous enamels
- H01B3/084—Glass or glass wool in binder
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B3/00—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties
- H01B3/18—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances
- H01B3/30—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes
- H01B3/36—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes condensation products of phenols with aldehydes or ketones
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- 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
- H01F1/12—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 soft-magnetic materials
- H01F1/14—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 soft-magnetic materials metals or alloys
- H01F1/20—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 soft-magnetic materials metals or alloys in the form of particles, e.g. powder
- H01F1/22—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 soft-magnetic materials metals or alloys in the form of particles, e.g. powder pressed, sintered, or bound together
- H01F1/24—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 soft-magnetic materials metals or alloys in the form of particles, e.g. powder pressed, sintered, or bound together the particles being insulated
- H01F1/26—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 soft-magnetic materials metals or alloys in the form of particles, e.g. powder pressed, sintered, or bound together the particles being insulated by macromolecular organic substances
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- Chemical & Material Sciences (AREA)
- Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Inorganic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Power Engineering (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Dispersion Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
A magnetodielectric material comprises iron and from 8 to 25% wt. of a thermosetting phenol-formaldehyde resin binder, from 5 to 20% wt. of a fibrous filler previously impregnated with a phenol-formaldehyde resin, and from 0.5 to 1.5% wt. of a lubricant. The filler may be asbestos powder, glass fibre or a synthetic resin fibre, e.g. polyethylene terephthalate. The binder may be modified with a polyolefin, a polyvinylacetal or colophony.
Description
SPECIFICATION
Magnetodielectric material
The present invention relates to a magnetodielectric material and to a process for producing such material.
This material is useful in electrical engineering, electronics, radio engineering and other industries.
A magnetodielectric material is known (see for example USSR copyright no. 169706 of 1965) which is iron-based and contains a thermosetting resin produced from furane and epoxy resins. Such a material has the following composition:
Furano-epoxy resin 100 parts by weight
Iron powder 250 parts by weight
Hardeners (hexamethylenediamine or polyethylenepolyamine ) 15 parts by weight
Glass fibre additive 1 - 1.5 parts by weight.
A magnetodielectric material which is iron-based and contains a filler in addition to a thermosetting resin is also known (see for example USSR copyright no. 524232 of 1976). In this case the material contains an epoxy-novolac block copolymer and has the following composition:
Epoxy-novolac block-copolymer 30 - 35 parts by weight
Urotropine 3 - 4 parts by weight
Phthalic anhydride 2 - 3 parts by weight
Filler 5 - 6 parts by weight
Iron the balance.
Known magnetodielectric materials have been found to have insufficiently good physical and mechanical properties, such as inadequate resistance to vibrational loads. This is because the properties of a magnetodielectric material are determined by the properties of the binder, and known binders are not sufficiently resilient.
We have now discovered a magnetodielectric material which has good physical, mechanical and magnetodielectrical properties, and the desired magnetic permeability. These good performance characteristics are due to the particular thermosetting resin used and to the interaction between the various components.
Thus, the present invention consists in a magnetodielectric material comprising iron and from 8 to 25% by weight of a thermosetting phenol formaldehyde binder, from 5 to 20% by weight of fibrous filler impregnated with a phenol formaldehyde resin, and from 0.5 to 1.5% by weight of a lubricant.
We prefer that the binder is a modified phenol formaldehyde resin, and suitable modifiers include: polyolefins; polyolefin derivatives; polyvinyl acetal; and calophony. The amount of modifier is preferably from 10 to 30% by weight based on the weight of the resin.
Any filler suitable for a phenol formaldehyde resin may be used, but we prefer asbestos powder, glass fibre or synthetic fibre.
Convenient lubricants include fatty acids and salts of fatty acids, and of these we prefer oleic acid, stearic acid and calcium stearate.
The present invention further consists in a process for producing a magnetodielectric material, which comprises compounding athermosetting phenol formaldehyde binderwith powdered iron to form a substantially homogeneous powdered substance, and mixing this substance in the presence of a lubricant with a fibrous filler impregnated with a phenol formaldehyde resin.
This material can then be compression moulded to form any suitable moulded article.
Variation of the composition of the components (especially of the binder) and preliminary impregnation of the filler mean that improved physical and mechanical properties, magnetic permittivity and performance characteristics can be achieved.
The thermosetting binder may comprise a modified and/or non-modified novolac and/or resol type phenol formaldehyde resin. Where a novolac type resin is used a hardener should be employed, for example, hexamethylenetetramine. Any suitable modifier may be used, but we prefer polyolefins, polyolefin derivatives, polyvinylacetals and calophony. The preferred weight of modifier is from 10 to 30% based on the weight of the resin. Suitable fillers include asbestos fibre, glass fibre and synthetic fibres such as polyethylene terephthalate. Fibrous filler is impregnated with phenol formaldehyde resin (preferably using a 20 - 60% solution) and the impregnated filler is then mixed with the remainder of the components.The resin used to impregnate the filler may be, but need not be, the same type of resin as that with which the impregnated filler is mixed.
The preferred techniques for making the magnetodielectric material are similar two conventional methods of manufacturing phenol plastics. Two such techniques are as follows.
The first technique uses a dry resin. A thermosetting binder plus lubricant is compounded with iron powder to mechanically disperse the components. The resultant composition is homogenised using rollers, and then powdered. This powder together with a fibrous filler previously impregnated with the same binder are then fed to a mixer. Articles may be produced from the product by compression moulding. This technique is suitable when the filler is a glass fibre filler.
The second technique uses an emulsified resin. A mixer is charged with a lubricant, iron powder, and a thermosetting binder in the form of a 40 - 90% alcoholic solution. After compounding the iron powder and the binder, fibrous filler impregnated with the same binder is added to the mixer. The resulting composition is then homogenized using water-cooled non-friction rollers, and dried at 60 - 90"C to the desired fluidity.
The invention is further illustrated by the following examples. Unless otherwise stated all amounts are given as percent by weight.
Example I
A novolac phenol formaldehyde resin (15.5), hexamethylenetetramine (3), calcium stearate (0.7) and iron powder (66.8) were charged into a mixer. The components were stirred for 60 minutes, and the resulting mixture was homogenized for from 6 to 10 minutes using friction rolls at a working roll temperature of from 70 to 1000C and an idle roll temperature of from 105 to 140on. The rolled mass was then cooled and comminuted. The resulting composition was mixed with chopped glass fibre (14) which had been previously impregnated with resol phenol formaldehyde resin. The magnetodielectric material thus produced was processed into articles using a conventional method for processing phenol plastics.
Example 2
Resol phenol formaldehyde resin (8), calcium stearate (0.5) and iron powder (71.5) were charged into a mixer, and stirred for 40 - 50 minutes. The resulting mixture was rolled and comminuted. The comminuted composition was then mixed with chopped glass fibre (20) which had been previously impregnated with phenol formaldehyde resin.
Example 3
Resol phenol formaldehyde resin (25) modified with chlorosulphonated polyethylene, calcium stearate (1) and iron powder (69) were charged into a mixer and stirred until a homogenous mixture was obtained. The resulting mixture was rolled, comminuted and then mixed with glass fibre (5) impregnated with a resol phenol formaldehyde resin.
Example 4
Emulsified phenol formaldehyde resin (9) modified with polyvinylbutyral, oleic acid (1.5) and hexamethylenetetramine (1.5) were charged into a mixer and stirred for 20 - 30 minutes. Iron powder (79) was then introduced into the mixer and stirring was continued for a further 30 - 40 minutes. The resulting mixture was rolled at room temperature without friction in water-cooled rolls, and then dried and comminuted. The composition that resulted was mixed with glass fibre (9) which had previously been impregnated with a resol phenol formaldehyde resin.
Example 5
Emulsified phenol formaldehyde resin (10) modified with calophony, oleicacid (0.5) and asbestos fibre (10) were charged into a mixer. Mixing was continued until the fibre was completely impregnated. Then, the same resin (10) arid iron powder (69.5) were introduced into the mixer, and stirring was continued for 40 - 50 minutes. The resulting mixture was homogenized in rolls without friction, and subsequently dried and comminuted.
Example 6
Emulsified phenol formaldehyde resin (8) and iron powder (71.3) were charged into a mixer, stirred for 30 minutes, and then discharged, dried and comminuted. Then the same resin (8), stearic acid (0.7) and polyethylene terephthalate fibre (12) were charged into a mixer causing the fibre to be impregnated. Then, the compounded and dried iron powder was introduced into the mixer, and all of the components were stirred for 20 - 30 minutes. The resulting mixture was rolled and dried.
Such magnetodielectric moulding material may be used in the manufacture of components of electrical machines, for example magnetic slot wedges. Typical magnetodielectric material according to the invention has the following properties:
Density 3.5 - 4.5 g/cm3
Impact viscosity 10 - 30 kgf cm/cm2
ultimate bending strength 600 - 1,000 kgf/cm2
compression strength 1,300 - 2,000 kgf/cm2
Martens thermal staility 120 - 200or Brinell hardness, 4,000 - 7,500 kgf/cm2
permittivity at H=3,000 3.0 - 8.0 A/cm
shrinkage 0.2 - 0.5%
operating time under extreme condition 50,000 - 60,000 h.
The magnetodielectric material was found to be stable to heat: the properties of the material did not change after heating at 200"C for 14 days.
The efficiency of slot wedges for electrical machines can be improved by 1 - 2% by using the material of the invention. The material of the invention also reduces over heating, reduces vibroacoustic noises and improves the reliability of the machines.
Claims (18)
1. A magnetodielectric material comprising iron and from 8 to 25% by weight of a thermosetting phenol formaldehyde binder, from 5 to 20% by weight of a fibre filler impregnated with a phenol formaldehyde resin, and from 0.5 to 1.5% by weight of a lubricant.
2. A material according to claim 1, in which the binder is a modified phenol formaldehyde resin.
3. A material according to claim 2, in which the modifier is a polyolefin, a polyolefin derivative, a polyvinylacetal or calophony.
4. A material according to claim 2 or claim 3, in which the amount of modifier is from 10 to 30% by weight based on the weight of the resin.
5. A material according to any one of the preceding claims, in which the filler is asbestos powder, glass fibre our a syntheticfibre.
6. A material according to any one of the preceding claims, in which the lubricant is a fatty acid or a salt of a fatty acid.
7. A material according to claim 6, in which the lubricant is oleic acid, stearic acid or calcium stearate.
8. A material according to claim 1, substantially as herein described with reference to any one of the foregoing examples.
9. A process for producing a magnetodielectric material, which comprises compounding a thermosetting phenol formaldehyde binder with powdered iron to form a substantially homogeneous powdered substance, and mixing this substance in the presence of a lubricant with a fibrous filler impregnated with a phenol formaldehyde resin.
10. A process according to claim 9, in which the binder is a modified phenol formaldehyde resin.
11. A process according to claim 10, in which the modifier is a polyolefin, a polyolefin derivative, a polyvinylacetal or calophony
12. A process according to claim 10 or claim 11, in which the amount of modifier is from 10 to 30% by weight based on the weight of resin.
13. A process according to any one of claims 9 to 12, in which the filler is asbestos powder, glass fibre or a synthetic fibre.
14. A process according to any one of claims 9 to 13, in which the lubricant is a fatty acid or a salt of a fatty acid.
15. A process according to claim 14, in which the lubricant is oleic acid, stearic acid or calcium stearate.
16. A process according to claim 9, substantially as herein described with reference to any one of the foregoing examples.
17. A magnetodielectric material when produced by a process according to any one of claims 9 to 16.
18. A process for producing a moulded article, in which a magnetodielectric material according to any one of claims 1 to 8 and 17 is compression moulded.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB7835272A GB2035344B (en) | 1978-09-01 | 1978-09-01 | Magnetodielectric material |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB7835272A GB2035344B (en) | 1978-09-01 | 1978-09-01 | Magnetodielectric material |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| GB2035344A true GB2035344A (en) | 1980-06-18 |
| GB2035344B GB2035344B (en) | 1982-11-03 |
Family
ID=10499389
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB7835272A Expired GB2035344B (en) | 1978-09-01 | 1978-09-01 | Magnetodielectric material |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB2035344B (en) |
-
1978
- 1978-09-01 GB GB7835272A patent/GB2035344B/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| GB2035344B (en) | 1982-11-03 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PCNP | Patent ceased through non-payment of renewal fee |