EP0637363A1 - Friction material - Google Patents

Friction material

Info

Publication number
EP0637363A1
EP0637363A1 EP93908018A EP93908018A EP0637363A1 EP 0637363 A1 EP0637363 A1 EP 0637363A1 EP 93908018 A EP93908018 A EP 93908018A EP 93908018 A EP93908018 A EP 93908018A EP 0637363 A1 EP0637363 A1 EP 0637363A1
Authority
EP
European Patent Office
Prior art keywords
friction material
friction
reactive metal
reactive
calcium
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.)
Withdrawn
Application number
EP93908018A
Other languages
German (de)
French (fr)
Inventor
Alan William Atkinson
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Federal Mogul Technology Ltd
Original Assignee
T&N Technology Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by T&N Technology Ltd filed Critical T&N Technology Ltd
Publication of EP0637363A1 publication Critical patent/EP0637363A1/en
Withdrawn legal-status Critical Current

Links

Classifications

    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F16ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
    • F16DCOUPLINGS FOR TRANSMITTING ROTATION; CLUTCHES; BRAKES
    • F16D69/00Friction linings; Attachment thereof; Selection of coacting friction substances or surfaces
    • F16D69/02Compositions of linings; Methods of manufacturing
    • F16D69/027Compositions based on metals or inorganic oxides
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/02Elements
    • C08K3/08Metals
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F16ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
    • F16DCOUPLINGS FOR TRANSMITTING ROTATION; CLUTCHES; BRAKES
    • F16D69/00Friction linings; Attachment thereof; Selection of coacting friction substances or surfaces
    • F16D69/02Compositions of linings; Methods of manufacturing
    • F16D69/025Compositions based on an organic binder

Landscapes

  • Engineering & Computer Science (AREA)
  • General Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Mechanical Engineering (AREA)
  • Inorganic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Braking Arrangements (AREA)

Abstract

A friction material e.g. for a brake pad or lining, has a reactive metal selected from calcium, lithium, sodium, and potassium, distributed therein. As the reactive metal becomes exposed in service, it reacts with water to form a highly alkaline hydroxide which acts to combat 'corrosion stiction'.

Description

FRICTION MATERIAL
This invention is concerned with friction material, for example friction material for use in brake pads or brake linings for vehicles or machinery.
It is well known that brake pads or linings can suffer from corrosion problems in service. In particular, a phenomenon known as "corrosion-stiction" can under wet conditions cause the friction material to stick to the rotor (disc or drum) with the brakes applied. Corrosion- stiction occurs especially in humid conditions or when the friction material becomes contaminated with salt. It is also well known that the likelihood of corrosion-stiction can be reduced or eliminated by the incorporation of an alkali material in the friction material. In some formulations of friction material, tealcium hydroxide in powder form is included. Calcium hydroxide has the advantages that it is relatively cheap and has a low solubility so that it is not readily washed out of the friction material during service.
Most modern friction material formulations include cross-linkable polymers as a binder. For example, phenolic resins are commonly used for this purpose. It is found that, if calcium hydroxide is included in such formulations, premature cross-linking of the polymer during mixing of the formulation can occur, resulting in an unusable material that can not be moulded into a fully dense brake pad or lining. Where such formulations are involved, therefore, the calcium hydroxide cannot be added to combat corrosion-stiction. In British Patent Application number 9303279.5, filed on the 18th February 19930, a method is described by which an alkali material can be incorporated in a friction material r and in which the alkali material is separated from the binder of the friction material but is available to combat corrosion-stiction, is described. This method involves encapsulating particles of alkali material in a coating material which is substantially inert in relation to the uncured binder, the coating material, however, being capable of being abraded from the particles to expose the alkali material as the friction material wears in service. However, although this method incorporates alkali, the alkali and the coating material therefor has to be added to the friction material at the expense of other materials which contribute to the friction characteristics of the material, the alkali and the coating therefor giving substantially no contribution to the friction characteristics. Furthermore, the encapsulation of the alkali material is somewhat complex.
It is an object of the present invention to provide a friction material in which alkali material becomes available during service to combat corrosion-stiction, in which the above-mentioned disadvantages are avoided.
The invention provides a friction material characterised in that the material has a reactive metal selected from calcium, lithium, sodium and potassium distributed therein which, as it becomes exposed due to wear of the friction material in service, is capable of reacting with water to form a highly alkaline hydroxide.
A friction material according to the invention does not have added alkali material but rather the alkali is created as the reactive material becomes exposed at points where it is needed. Thus, alkali material is made available as required without the disadvantages of the method of the above-mentioned patent application. The required water can be obtained from atmospheric moisture. Where the material is described herein as being capable of reacting with water to form a highly active alkaline hydroxide, it is not intended to exclude a two-stage reaction in which the hydroxide is produced from an intermediate compound, e.g. where calcium is used this may first react with atmospheric oxygen to form calcium oxide which then reacts with atmospheric water to form calcium hydroxide. Furthermore, the unreacted metal can contribute to the friction characteristics.
The reactive metal may be present as an intermetallic compound, for example calcium silicide (about 30% of calcium and 70% of silicon) or calcium aluminide (about 75% of calcium and 25% of aluminium) . These intermetallic compounds have the advantage of not being as reactive as some of the metals aforementioned so that they can be more easily handled during the formation of the friction material.
The reactive metal may be alloyed before incorporation in the friction material to reduce its reactivity and thereby make it easier to handle or it may be encapsulated in a capping material which is not reactive with other materials in the friction material. The capping material may, for example, be a resin or an oxide or other compound formed by chemical reaction on the surface of the material. If desired, the metal may be both alloyed and capped. Also the aforementioned intermetallic compounds may be capped.
In addition to giving the advantage of being available to create alkali as the friction material wears, the above- identified metals also give cathodic protection against electrolytic corrosion. It is known to add metals to friction materials for this purpose, such as zinc or aluminium, but these metals produce hydroxides which are insufficiently soluble to enable effective combating of corrosion-stiction. It is desirable to aim for an alkali giving a pH greater than or equal to 12.
Some of the reactive metals mentioned above as possible reactive materials, can also be used to provide reinforcement for the friction material. It is known to add metals such as steel, copper or brass as reinforcement, for example in the form of fibres or wires but known reinforcements are not reactive. Where it is intended that the reactive metal should also assist in reinforcement, the reactive metal may be provided in the- form of flakes, or as fibres, or as wires.
It is also known to add metals to conventional friction materials to alter their friction and wear properties. Fine powders of copper, brass or sponge iron are commonly used for this purpose. They reduce variations in coefficient of friction under changing braking conditions and can also reduce wear rates.
There now follows an illustrative example of a friction material in accordance with the invention.
For comparison purposes, brake pads were prepared from a conventional mixture of powdered phenolic resin, reinforcing fibres, fillers, graphite powder and metal particles (15% by weight) . The metal particles were of brass (approximately 0.5mm in diameter). In the illustrative example, an identical mixture was used for preparing further brake pads but with the brass particles replaced by the same weight percentage of similarly sized particles of a calcium silicon alloy/inter-metallic compound (30% by weight calcium and 70% by weight silicon) .
When the brake pads had cured, they were abraded to simulate the wear in service and to reveal fresh surfaces within the pads thereby exposing metallic particles of the brass or of the alloy/inter-metallic compound. The abraded surfaces were moistened and their pH values were measured using indicator papers. For the pads containing the brass particles, the pH value was approximately 7, i.e. insufficient to inhibit corrosion stiction. For the pads containing the alloy/inter-metallic compound, the pH value was above 12, i.e. sufficient to inhibit corrosion stiction.

Claims

A friction material characterised in that the material has a reactive metal selected from calcium, lithium, sodium and potassium distributed therein which, as it becomes exposed due to wear of the friction material in service, is capable of reacting with water to form a highly alkaline hydroxide.
A friction material according to Claim 1, characterised in that the metal is alloyed before incorporation in the friction material.
A friction material according to Claim 1, characterised in that the reactive metal is in the form of an intermetallic compound.
A friction material according to any one of Claims 1 to 3, characterised in that the reactive metal is encapsulated in a capping material which is not reactive with other materials in the friction material before incorporation in the friction material.
A friction material according to any one of Claims l to 4, characterised in that the reactive metal is in the form of a fibre or a wire.
EP93908018A 1992-04-23 1993-04-08 Friction material Withdrawn EP0637363A1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GB9208819 1992-04-23
GB929208819A GB9208819D0 (en) 1992-04-23 1992-04-23 Friction material
PCT/GB1993/000751 WO1993022580A1 (en) 1992-04-23 1993-04-08 Friction material

Publications (1)

Publication Number Publication Date
EP0637363A1 true EP0637363A1 (en) 1995-02-08

Family

ID=10714454

Family Applications (1)

Application Number Title Priority Date Filing Date
EP93908018A Withdrawn EP0637363A1 (en) 1992-04-23 1993-04-08 Friction material

Country Status (4)

Country Link
EP (1) EP0637363A1 (en)
AU (1) AU3901193A (en)
GB (2) GB9208819D0 (en)
WO (1) WO1993022580A1 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111720464A (en) * 2020-06-18 2020-09-29 青岛理工大学 Brake pad with low wear rate and preparation method thereof

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE102012203760A1 (en) 2012-03-09 2013-09-12 Robert Bosch Gmbh friction brake lining

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1288124A (en) * 1970-01-23 1972-09-06
GB1355244A (en) * 1970-05-21 1974-06-05 Mitsui Shipbuilding Eng Prefabrication primer for high tensile steel
US3898361A (en) * 1973-06-04 1975-08-05 Caterpillar Tractor Co Fluoroelastomer-based composite material
BE844043R (en) * 1975-07-14 1977-01-12 COMPOSITE MATERIAL BASED ON FLUORINE ELASTOMERS
FR2521240B1 (en) * 1982-02-05 1987-03-27 Valeo FRICTION LINING, PARTICULARLY FOR BRAKES, CLUTCHES AND OTHER APPLICATIONS

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO9322580A1 *

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111720464A (en) * 2020-06-18 2020-09-29 青岛理工大学 Brake pad with low wear rate and preparation method thereof
CN111720464B (en) * 2020-06-18 2022-05-27 青岛理工大学 Brake pad with low wear rate and preparation method thereof

Also Published As

Publication number Publication date
GB9208819D0 (en) 1992-06-10
GB9307533D0 (en) 1993-06-02
GB2266312B (en) 1995-09-20
AU3901193A (en) 1993-11-29
WO1993022580A1 (en) 1993-11-11
GB2266312A (en) 1993-10-27

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