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Brake pad
View on WikipediaBrake pads are a component of disc brakes used in automotive and other applications. Brake pads are composed of steel backing plates with friction material bound to the surface that faces the disc brake rotor .
Function
[edit]Brake pads convert the kinetic energy of a vehicle to thermal energy through friction. Two brake pads are contained in the brake with their friction surfaces facing the rotor.[1] When the brakes are hydraulically applied, the caliper clamps or squeezes the two pads together onto the spinning rotor to slow and stop the vehicle. When a brake pad heats up due to contact with the rotor, it transfers small amounts of its friction material onto the disc, leaving a dull grey coating on it. The brake pad and disc (now both having the friction material), then "stick" to each other, providing the friction that stops the vehicle.
In disc brakes, there are usually two brake pads per disc rotor, they both function together. These are held in place and actuated by a caliper affixed to the wheel hub or suspension upright. Racing calipers, however, can utilize up to six pads, with varying frictional properties in a staggered pattern for optimum performance. Depending on the properties of the material, the weight of the vehicle and the speeds it is driven at, disc wear rates may vary. The brake pads must usually be replaced regularly (depending on pad material). Most brake pads are equipped with a method of alerting the driver when this needs to be done. A common technique is manufacturing a small central groove whose eventual disappearance by wear indicates the end of a pad's service life. Other methods include placing a thin strip of soft metal in a groove, such that when exposed (due to wear) the brakes squeal audibly. A soft metal wear tab can also be embedded in the pad material that closes an electric circuit when the brake pad wears thin, lighting a dashboard warning light.
History
[edit]The concept of brake pads or disc brakes as an alternative to drum brakes had been around at least as early as a patent by F. W. Lanchester in 1902.[2] However, due to high cost and inefficiencies compared to drum brakes they were not commonly implemented until after World War II.[3] Once disc brake technology improved, brake performance quickly surpassed that of drum brakes. The performance difference was most noticeably exhibited in 1953 when a Jaguar outfitted with brake pads won the 24 Hours of Le Mans Grand Prix of Endurance race.[3][4] The success of the Jaguar is commonly attributed to the car’s disc brakes, which allowed the drivers to approach turns faster and brake later than their opponents, which ultimately led to its victory. As late as 1963 the majority of automobiles using disc brakes were European made, with American cars adopting the technology in the late 1960s after the invention of fixed calipers that made installation cheaper and more compact.[3]
Technology
[edit]Disc brake advantages
[edit]Disc brakes offer better stopping performance as compared to drum brakes. They provide better resistance to "brake fade" caused by the overheating of brake pads, and are also able to recover quickly from immersion (wet brakes are less effective). Unlike a drum brake, a disc brake has no self-servo effect—the braking force is always proportional to the pressure applied on the braking pedal lever. However many disc brake systems have servo assistance ("Brake Booster") to reduce the driver's pedal effort.[citation needed]
Disc brake pads are easier to inspect and replace than drum brake friction lining.
Types
[edit]
There are numerous types of brake pads, depending on the intended use of the vehicle, from very soft and aggressive (such as racing applications) to harder, more durable and less aggressive compounds. Most vehicle manufacturers recommend a specific kind of brake pad for their vehicle, but compounds can be changed (by either buying a different make of pad or upgrading to a performance pad in a manufacturer's range) according to personal tastes and driving styles. Care must always be taken when buying non-standard brake pads as the operating temperature ranges may vary, such as performance pads not braking efficiently when cold or standard pads fading under hard driving. In cars that suffer from excessive brake fade, the problem can be minimized by installing better quality and more aggressive brake pads.
Materials
[edit]The most important characteristics that are considered when selecting a brake pad material are as follows:
- The material's ability to resist brake fade, caused by an increase in temperature the material will experience from the conversion of kinetic energy into thermal energy.[5][6]
- The effects of moisture on brake fade. All brakes are designed to withstand at least temporary exposure to water.[5][6]
- The ability to recover quickly from increased temperature or moisture, and exhibit approximately the same friction levels at any point in the drying or cooling process.[5][6]
- The friction coefficient of modern brake pads should be low enough prevent locking of the wheels but high enough to provide sufficient stopping power. Friction coefficients are typically between 0.3 and 0.5 for brake pad materials.[6]
- The ability to resist wear due to friction, but not to the extent that rotor wear occurs more quickly than brake material is sacrificed.[5][6]
- The ability of the material to provide smooth and even contact with the rotor or drum, instead of a material that breaks off in chunks or causes pits, dents, or other damage to the surface in contact.[5][6]
- The ability to apply appropriate frictional force while also operating quietly.[6]
Another material requirement that is considered is how compressible the brake pads are; if they are too compressible then brake travel or brake booster fluid displacement can be excessive.[7] Brake pad material must also be porous to minimize the effect water has on the friction coefficient.[7]
Asbestos was added as a common ingredient to brake pads post-WWI, as car speeds began to increase, because research showed that its properties allowed it to absorb the heat (which can reach 500 °F) while still providing the friction necessary to stop a vehicle.[8] However, as the serious health-related hazards of asbestos eventually started to become apparent, other materials had to be found. Asbestos brake pads have largely been replaced by non-asbestos organic (NAO) materials in first world countries.[9] Today, brake pad materials are classified into one of four principal categories, as follows:
- Non-metallic materials – these are made from a combination of various synthetic substances bonded into a composite, principally in the form of cellulose, aramid, PAN, and sintered glass. They are gentle on rotors, but produce a fair amount of dust, thus having a short service life.
- Semi-metallic materials – synthetics mixed with varying proportions of flaked metals. These are harder than non-metallic pads, more fade-resistant and longer lasting, but at the cost of increased wear to the rotor/drum which then must be replaced sooner. They also require more actuating force than non-metallic pads in order to generate braking torque.
- Fully metallic materials – these pads are used only in racing vehicles, and are composed of sintered steel without any synthetic additives. They are very long-lasting, but require more force to slow a vehicle while wearing off the rotors faster. They also tend to be very loud.
- Ceramic materials – Composed of clay and porcelain bonded to copper flakes and filaments, these are a good compromise between the durability of the metal pads, grip and fade resistance of the synthetic variety. Their principal drawback, however, is that unlike the previous three types, despite the presence of the copper (which has a high thermal conductivity), ceramic pads generally do not dissipate heat well, which can eventually cause the pads or other components of the braking system to warp.[5] However, because the ceramic materials cause the braking sound to be elevated beyond that of human hearing, they seem exceptionally quiet.[10]
Phenol formaldehyde resin is frequently used as a binding agent. Graphite can serve as a friction material as well as binding agent.[11] Another friction material commonly used is zirconium silicate.[9] An Italian producer is conducting research to use cement as a cheap and less energy-intensive binding agent.[12] The table below outlines the make up of a common brake pad.[9]
| Constituent | % by weight |
| Whiting (Chalk) | 31.6 |
| Bronze powder | 15 |
| Graphite | 10 |
| Vermiculite | 16 |
| Phenolic resin | 16 |
| Steel fibres | 6 |
| Rubber particles | 5 |
| "Friction Dust" | 5 |
| Sand | 3 |
| Aramid fibres | 2 |
There are environmental factors that govern the selection of brake pad materials. For example, the bill SSB 6557[13] adopted in Washington State in 2010 limits the amount of copper that is allowed to be used in friction materials, to be eventually phased out to trace amounts, due to the negative impact of high copper levels on aquatic life. For its substitution, different material combinations have been developed, though no direct replacement is available yet.[14] Other materials, such as compounds made with antimony, are being studied.
Vehicles have different braking requirements. Friction materials offer application-specific formulas and designs. Brake pads with a higher coefficient of friction provide good braking with less brake pedal pressure requirement, but tend to lose efficiency at higher temperatures. Brake pads with a smaller and constant coefficient of friction do not lose efficiency at higher temperatures and are stable, but require higher brake pedal pressure.
Maintenance and troubleshooting
[edit]Brake pads should be checked at least every 5,000 miles for excessive or uneven wear. Although brake pad wear is unique to each vehicle, it is generally recommended that brake pads be replaced every 50,000 miles,[6] while brake discs (or rotors) typically last longer, needing replacement every 70,000 miles.
Malfunctions with brake pads can have many effects on the performance of a vehicle. The following chart outlines some common issues that can be caused by brake pad malfunctions:[8]
| Issue | Possible Cause |
|---|---|
| Braking requires an abnormal amount of force
on brake pedal |
Worn brake pads, contaminated brake fluid, faulty brake caliper, faulty master cylinder, loss of vacuum, loss of brake fluid |
| Car pulls to one side when braking | Faulty brake caliper, restriction in hydraulic system, brake pad lining(s) contaminated with oil or brake fluid, brake pads not replaced in pairs, brake pad not fitted correctly, |
| Poor braking performance | Brake pad lining(s) soaked with water, oil, or
brake fluid; Overheated brake pad linings, worn brake pads, faulty master cylinder, brake fluid leak, air in brake fluid, misadjusted brake shoes, boiling brake fluid |
| Sensitive braking | Incorrect brake pad linings; Greasy brake pad linings, faulty proportioning valve, misadjusted master cylinder pushrod |
| Noisy braking (grinding or screeching sounds
when braking) |
Extremely worn brake pads, brake pad(s) not fitted correctly, faulty or missing brake pad shim, brake pad wear indicator |
| Vibration under braking | Contaminated rotors or pads, warped rotors, out of round drums, ABS activation |
Testing of materials
[edit]The National Bureau of Standards (NBS) started testing of brake material in the US in 1920. The testing setup was then shared with manufacturers who wanted them so that they could begin to test their own products.[15] Over time the NBS continued to develop new instruments and procedures for testing pads and lining, and these standards eventually became the standards for the American Engineering Standards Committee's Safety Code for Brakes and Brake Testing.[15]
SAE J661 testing is used to determine the friction of different brake pad materials by testing a 1 inch (25 mm) square liner with a brake drum. This testing yields values for both hot and cold coefficients of friction, which are then paired with letter designations.[7] The table below outlines what letter goes with each range for the coefficient of friction. An example of the designation would be "GD", where "G" is the normal coefficient, while the "D" represents heated.[7]
| Letter Designation for Friction Coefficients | |
| C | <0.15 |
| D | 0.15 to 0.25 |
| E | 0.25 to 0.35 |
| F | 0.35 to 0.45 |
| G | 0.45 to 0.55 |
| H | >0.50 |
| Z | unclassified |
Cataloguing
[edit]There are different systems for the cataloguing of brake pads. The most frequently used system in Europe is the WVA numbering system.[16]
The cataloguing system used in North America, and recognized around the world, is the standardized part numbering system for brakes and clutch facings issued by the Friction Materials Standards Institute (FMSI). FMSI's mission is to, "Maintain and enhance this standardized part numbering system for all on highway vehicles in use in North America."[17]
Cartridge brake pad
[edit]A type of brake pad used on rim brakes.
See also
[edit]References
[edit]- ^ Henderson, Bob; Haynes, John H. (1994). "Disc Brakes". The Haynes Automotive Brake Manual. Haynes North America. pp. 1–20.
- ^ Newcomb, T. P. (1989). A technical history of the motor car. Spurr, R. T. Bristol, England: A. Hilger. ISBN 0852740743. OCLC 18984114.
- ^ a b c Mom, Gijs, 1949- (2014). The evolution of automotive technology : a handbook. Warrendale, Pennsylvania. ISBN 9780768080278. OCLC 883510695.
{{cite book}}: CS1 maint: location missing publisher (link) CS1 maint: multiple names: authors list (link) CS1 maint: numeric names: authors list (link) - ^ Tremayne, David. (2009). The science of Formula 1 design : expert analysis of the anatomy of the modern Grand Prix car (3rd ed.). Sparkford, NR Yeovil, Somerset, U.K.: Haynes Pub. ISBN 9781844257188. OCLC 430838880.
- ^ a b c d e f Cliff Owen (21 June 2010). Today's Technician: Automotive Brake Systems Classroom and Shop Manual. Cengage Learning. pp. 27–28. ISBN 978-1-4354-8655-3.
- ^ a b c d e f g h Nunney, M. J. (Malcolm James) (1998). Automotive technology. Society of Automotive Engineers. (3rd ed.). Warrendale, PA: SAE. ISBN 0768002737. OCLC 40160726.
- ^ a b c d Limpert, Rudolf. (1999). Brake design and safety (2nd ed.). Warrendale, Pa.: Society of Automotive Engineers. ISBN 1560919159. OCLC 40479691.
- ^ a b Crouse, William Harry (1971). Automotive chassis and body: construction, operation, and maintenance (4th ed.). New York: McGraw-Hill. ISBN 007014690X. OCLC 136535.
- ^ a b c Elmarakbi, Ahmed. (2013). Advanced Composite Materials for Automotive Applications : Structural Integrity and Crashworthiness. Hoboken: Wiley. ISBN 9781118535271. OCLC 861080217.
- ^ Owen 2010 p162
- ^ Entry on brake pads (Bremsbelag) in Kfz-Tech.de
- ^ Essay Forschungsprojekt Cobra - Die Bremse der Zukunft besteht aus Zement, February 2015 in: Ingenieur.de
- ^ "Limiting the use of certain substances in brake friction material. SB 6557 - 2009-10". apps.leg.wa.gov. January 29, 2010. Archived from the original on 2010-01-30. Retrieved 2024-10-15.
- ^ Rampin, Ilaria; Zanon, Matteo; Echeberria, Jon; Loreto, Antonio Di; Martinez, Anemaite (2014-05-19). "Development of copper-free low steel brake pads for passenger cars". PM 2014: 3rd World Congress on Powder Metallurgy and Particulate Materials: 18–22.
- ^ a b Vinsel, Lee (2016). "Virtue via Association: The National Bureau of Standards, Automobiles, and Political Economy, 1919–1940". Enterprise & Society. 17 (4): 809–838. doi:10.1017/eso.2015.61. S2CID 156230896.
- ^ "WVA numbering system". Archived from the original on 2014-07-13. Retrieved 2009-10-05.
- ^ "Friction Materials Standards Institute". fmsi.org.
Brake pad
View on GrokipediaFunction and Principles
Basic Operation in Disc Brakes
In disc brake systems, brake pads serve as the primary frictional elements that interface with a rotating disc, or rotor, mounted to the wheel hub. The rotor, typically made of cast iron or composite materials, spins with the wheel assembly. When braking is initiated, hydraulic pressure from the master cylinder—generated by the driver's pedal force—is transmitted via fluid-filled lines to the brake caliper straddling the rotor.[9][10] The caliper contains one or more pistons on the inboard side that extend under this pressure to press the inner brake pad directly against the rotor's inner face. In fixed-caliper designs, opposing pistons actuate both pads simultaneously; in floating-caliper designs, the caliper body slides or pivots, allowing the outboard pad to contact the rotor's outer face via reaction force. This dual-sided clamping generates a normal force perpendicular to the rotor surface, with typical actuation pressures reaching 1,000 to 2,000 psi in passenger vehicles, depending on system design and load.[11][12][13] Friction arises from the intimate contact between the pad's friction material—composed of compounds like semi-metallics or organics bonded to a backing plate—and the rotor. This interaction opposes the rotor's tangential motion, producing a braking torque proportional to the coefficient of friction (typically 0.3 to 0.5 for standard pads) multiplied by the applied normal force and effective radius. The process converts the vehicle's kinetic energy into heat, with braking from 60 mph (97 km/h) generating approximately 200,000 to 500,000 joules per wheel, depending on vehicle mass and deceleration rate.[9][14][1] Upon pedal release, return springs retract the pistons and pads, minimizing drag and allowing the rotor to resume free rotation. The rotor's ventilated or slotted design facilitates convective and radiative heat dissipation, maintaining operational temperatures below fade thresholds (around 500–600°C for most materials) to ensure consistent performance. Over repeated cycles, abrasive wear erodes the pad material at rates of 0.1–0.2 mm per 1,000 km under average use, eventually requiring replacement when thickness falls below 2–3 mm.[15][12][16]Physics of Friction and Heat Dissipation
In disc brake systems, friction arises from the sliding contact between the brake pads and the rotating disc, where the pads' friction material interfaces with the disc surface under applied normal force from the caliper pistons. The coefficient of friction μ, typically ranging from 0.3 to 0.7 depending on pad material and operating conditions, quantifies the tangential resistive force f = μ N relative to the normal force N.[17] This force generates braking torque T = f r_eff, with r_eff as the effective radius of friction (often approximating 80-90% of the disc's outer radius due to pad contact area).[18] The process relies on kinetic friction, as the pad and disc exhibit relative sliding velocity until synchronization or stop, converting mechanical work into heat via inelastic deformation and microscopic adhesion at asperities.[19] The heat generated Q during braking equals the vehicle's kinetic energy dissipated, Q = (1/2) m v^2 for a single stop (neglecting rolling resistance), partitioned primarily to the disc (60-80%) and pads (20-40%) based on thermal effusivity and contact duration.[20] Instantaneous power dissipation P = f v_sliding = μ N ω r, where ω is angular velocity and v_sliding = ω r, peaks at high speeds and loads, with severe braking raising interface temperatures to 500-800°C.[21] For example, in a 1500 kg vehicle decelerating from 100 km/h, energy dissipation can exceed 200 kJ per brake, with frictional heat flux q = P / A_contact concentrated over the pad-disc interface area A_contact (typically 20-50 cm² per pad).[22] Material properties influence partitioning: pads with lower thermal conductivity (e.g., organic composites at ~0.5 W/m·K) retain more heat, while cast iron discs (~50 W/m·K) conduct it radially.[23] Heat dissipation occurs via convection to ambient air (dominant at velocities >10 m/s, with coefficients h ≈ 50-200 W/m²·K), conduction to the wheel hub and caliper, and minor radiation at high temperatures.[24] Vented disc designs enhance forced convection by channeling airflow through internal vanes, increasing effective h by 2-3 times compared to solid discs, though efficiency drops at low speeds where natural convection prevails (h ≈ 10-20 W/m²·K).[25] Transient temperature profiles follow the heat equation ∇·(k ∇T) + q = ρ c ∂T/∂t, with peaks at the friction surface decaying inward; inadequate dissipation causes thermal gradients leading to disc warping or pad material degradation, reducing μ by 20-50% above 400°C due to gasification or sintering.[26][27]Historical Development
Early Inventions and Drum Brake Precursors (Late 19th–Early 20th Century)
The initial braking mechanisms in late 19th-century automobiles were primitive, often adapting carriage-style wooden blocks or leather bands applied to wheels or drivetrain components for friction. Karl Benz's 1886 Patent-Motorwagen, widely recognized as the first practical automobile, featured a basic transmission brake operated by a hand lever that generated friction against the drive pulley to slow the vehicle.[28] These early systems provided marginal stopping power, as the materials—typically untreated leather or wood—degraded quickly from heat and abrasion, limiting their efficacy on motorized vehicles exceeding horse-drawn speeds.[29] Precursors to drum brake linings evolved from these external contracting band brakes, which wrapped flexible bands around a drum-like surface connected to the axle or transmission. By the turn of the century, internal expanding designs emerged, with the first documented use of a drum brake appearing in a Maybach automobile in 1900, where curved shoes pressed outward against the interior of a rotating metal drum to create friction.[30] This configuration offered mechanical advantages over external bands, including reduced exposure to road debris and improved leverage for actuation via cables or rods. Key advancements in friction materials coincided with drum brake adoption. In 1901, English inventor Herbert Frood patented brake blocks—early composite friction elements—for use on vehicle wheels, consisting of woven cotton fabric bound with linseed oil putty or resin to form durable, moldable linings attachable to brake shoes.[5][31] The following year, Louis Renault secured a patent for a refined drum brake, innovating by substituting woven asbestos for prior linings, which provided superior heat resistance and consistent friction coefficients, thereby addressing the rapid wear of organic materials in motorized applications.[32][33] These brake blocks and linings represented the direct antecedents to modern pads, prioritizing engineered composites for reliable torque transmission through controlled slippage and energy dissipation as heat.Asbestos Era and Mid-20th Century Standardization
The use of asbestos in brake linings emerged in the early 1900s as a response to the limitations of earlier friction materials like wood and leather, which degraded rapidly under heat and load. In 1902, the A.H. Raymond Company in Bridgeport, Connecticut, began producing automotive brake pads incorporating chrysotile asbestos for its high thermal resistance and durability, enabling sustained friction without excessive wear or fading.[34] By 1906, the company patented a design combining asbestos fibers with wire mesh, which improved structural integrity and heat dissipation in drum brake applications.[34] These innovations addressed the growing demands of motorized vehicles, where early brakes often failed due to overheating during prolonged use.[35] Throughout the mid-20th century, asbestos dominated brake pad formulations, typically comprising 30-50% chrysotile fibers mixed with phenolic resins, brass or copper powders, and sometimes steel wool for enhanced grip and noise reduction.[36] This composition provided consistent friction coefficients (often 0.3-0.5 under load) and resisted glazing or cracking at temperatures exceeding 300°C, outperforming alternatives in high-speed and heavy-duty applications.[37] Automobile manufacturers standardized asbestos-based pads for both drum and emerging disc brake systems, as seen in the post-World War II automotive boom, where production scaled to millions of vehicles annually; for instance, by the 1950s, nearly all U.S. passenger cars used asbestos linings to meet performance requirements for speeds up to 100 mph.[38] The material's low cost—derived from abundant chrysotile deposits—and manufacturability via compression molding further entrenched its use, despite early anecdotal reports of dust-related respiratory issues among mechanics.[39] Mid-20th-century standardization efforts focused on ensuring reliable friction and safety amid rising vehicle complexity and regulatory scrutiny. The Society of Automotive Engineers (SAE) developed protocols like J661 in the 1940s-1950s for dynamometer testing of friction materials, measuring wear rates and torque output under simulated braking cycles to classify pads by performance grades (e.g., "EE" for high-friction stability).[40] These standards facilitated interchangeability across manufacturers, reducing variability in stopping distances—typically 100-150 feet from 60 mph for contemporary sedans—and supported the transition to hydraulic disc brakes, first mass-adopted in models like the 1965 Ford Thunderbird.[41] Industry consortia also normalized asbestos content and curing processes to minimize fade, with formulations refined through empirical testing rather than advanced modeling, prioritizing empirical durability over emerging health data.[42] By the 1960s, such standardization correlated with federal safety pushes, though asbestos persisted due to its proven causal efficacy in heat management and wear resistance.[36]Post-Asbestos Transition and Material Regulations (1980s–Present)
The phase-out of asbestos in brake pads accelerated in the 1980s amid mounting evidence of its carcinogenic risks, particularly mesothelioma and lung cancer from fiber inhalation during manufacturing, installation, and repair. Major U.S. manufacturers voluntarily discontinued asbestos-containing friction materials in automotive brakes during this decade to mitigate liability from emerging litigation and regulatory scrutiny, shifting to alternatives like non-asbestos organic (NAO) compounds reinforced with aramid fibers, glass, or rubber, and semi-metallic formulations incorporating steel wool or copper fibers for enhanced durability and heat resistance.[43][44] In 1989, the U.S. Environmental Protection Agency (EPA) promulgated the Asbestos Ban and Phase-Out Rule under the Toxic Substances Control Act, which specifically prohibited future manufacture, import, and processing of asbestos in automotive brakes and linings after a phase-out period, though the rule was largely overturned by courts in 1991, leaving reliance on voluntary industry compliance.[45] In Europe, regulatory timelines varied but culminated in comprehensive bans: the United Kingdom prohibited asbestos in brake linings and pads effective January 1999 under health and safety directives, while the European Union extended its chrysotile asbestos restrictions to nearly all applications, including friction products, by January 2005 via Directive 2003/18/EC.[46] These transitions addressed occupational exposure risks, as brake dust generation during use and servicing could release respirable fibers, though subsequent toxicological analyses have noted that chrysotile asbestos in encapsulated brake formulations exhibits low biopersistence and limited pathogenicity compared to amphibole types, informing debates on the precautionary basis of outright bans.[46] Ceramic-based pads, introduced in the mid-1980s as premium alternatives, gained traction for their reduced noise, dust, and rotor wear, further diversifying options beyond NAO and semi-metallics.[3] Post-transition, environmental regulations targeted legacy components in replacement materials, particularly copper, which constitutes up to 10-20% in semi-metallic pads for thermal conductivity but contributes to aquatic toxicity via brake dust runoff. California enacted the first state-level mandate in 2010 (AB 346), requiring new brake pads sold after January 2021 to contain less than 5% copper by weight and under 0.5% after 2025, with Washington State adopting parallel limits via SB 6557.[47][48] The EPA facilitated a voluntary nationwide Copper-Free Brake Initiative in 2012, aligning manufacturers toward the same thresholds by 2025 to curb stormwater pollution, estimated at 1.3 million pounds of copper annually from vehicle braking in urban areas.[49] These measures prompted innovation in copper-free alloys and ceramics, balancing performance with ecological impacts, while aftermarket chrysotile uses faced final U.S. prohibition in 2024 under an EPA rule effective November 2024 for brakes.[50]Classification by Material
Organic and Non-Asbestos Organic (NAO) Pads
Organic and non-asbestos organic (NAO) brake pads consist primarily of a friction compound molded from organic fibers and resins, including aramid (Kevlar), glass fibers, rubber, graphite, and phenolic resins, bonded to a steel backing plate.[51][52] These materials were formulated as direct replacements for asbestos-based pads following health concerns over asbestos exposure, with widespread adoption accelerating after U.S. Environmental Protection Agency regulations in the 1980s restricted asbestos in friction products due to its carcinogenic risks.[29][53] In performance testing, NAO pads exhibit friction coefficients typically ranging from 0.35 to 0.45 under moderate braking conditions, providing stable stopping power comparable to legacy asbestos formulations but with higher sensitivity to temperature increases.[54][55] They generate lower noise levels due to the damping properties of organic fibers, producing less brake dust than semi-metallic alternatives and causing minimal wear on rotors.[56][57] However, their wear rates are elevated—often 20-50% higher than metallic pads in prolonged use—owing to the softer matrix, limiting lifespan to approximately 20,000-40,000 miles in standard passenger vehicle applications.[58][59] Heat dissipation in NAO pads is inferior to metallic or ceramic types, with fade onset occurring above 300-400°C, making them unsuitable for heavy-duty or high-performance scenarios where sustained braking generates excessive thermal loads.[60][61] This limitation stems from the lower thermal conductivity of organic binders, which prioritize low-noise operation over endurance under extreme conditions.[62] NAO formulations remain prevalent in original equipment for light-duty vehicles, emphasizing comfort and rotor preservation over aggressive friction demands.[6]Semi-Metallic Pads
Semi-metallic brake pads consist of friction materials incorporating 30% to 70% metallic components, primarily steel fibers, copper, iron, or graphite flakes, blended with organic binders, friction modifiers, and fillers such as aramid fibers or ceramics to achieve balanced performance.[63][64] This formulation enhances thermal conductivity compared to organic pads, allowing effective heat dissipation during repeated braking, with metal content typically ranging from 30% to 65% by volume to maintain structural integrity under high loads.[65][66] These pads exhibit friction coefficients between 0.35 and 0.45 under standard operating conditions, providing consistent stopping power suitable for demanding applications like towing or high-speed braking, where they outperform non-asbestos organic pads in fade resistance at temperatures exceeding 400°F.[66][67] Their metallic fibers contribute to higher shear strength and wear resistance, resulting in pad lifespans of 30,000 to 50,000 miles in passenger vehicles under mixed driving, though this varies with vehicle weight and usage intensity.[68][65] In performance evaluations, semi-metallic pads generate more rotor wear due to their abrasive metallic particles, accelerating disc glazing or grooving by up to 20-30% relative to ceramic alternatives, and they produce elevated brake dust levels—a normal byproduct of the braking process primarily consisting of iron particles from the cast iron rotors (approximately 80% of emissions) and friction material from the pads—appearing as dark or black residue on wheel rims. This accumulation may become noticeable over time due to gradual wear, increased braking frequency, changes in driving conditions, or mechanical issues such as sticking calipers causing brake drag and accelerated wear, often necessitating more frequent cleaning.[69][70][71] Additionally, their operation often involves increased noise from metal-to-metal contact, manifesting as squealing during low-speed stops or cold conditions, though chamfered edges and shims mitigate this in modern designs, and application of anti-squeal lubricants to the pad backing plate and caliper contact points during installation can further reduce vibrations and noise (see Maintenance and Replacement).[72][73] Commonly applied in trucks, SUVs, and performance cars requiring robust braking—such as those with gross vehicle weights over 5,000 pounds—semi-metallic pads suit environments with frequent heavy loads or aggressive driving, where their superior initial bite and modulation provide reliable control without excessive pedal effort.[74][65] Despite these strengths, their higher dust and noise profile limits widespread use in luxury or urban commuter vehicles favoring quieter operation.[75]Ceramic and Carbon-Ceramic Pads
Ceramic brake pads, developed in the mid-1980s as an alternative to metallic and organic formulations, primarily consist of ceramic fibers such as alumina and silicon carbide, combined with phenolic resin binders, copper fibers for heat transfer, and non-ferrous fillers.[3][76] This composition yields a denser material than semi-metallic pads, resulting in lower noise generation—often above the human hearing range—and significantly reduced brake dust compared to metallic types, with the dust produced being lighter in color, finer, and less prone to adhering to wheels; low-dust formulations prioritize reduced visible residue on wheels compared to semi-metallic pads, often minimal initially, though some accumulation may become noticeable over extended use due to gradual pad and rotor wear or varying driving conditions.[77][78] Compared to semi-metallic options, ceramic pads exhibit superior durability, with lifespans typically exceeding those of organic or semi-metallic pads under normal driving conditions, due to their resistance to warping and efficient heat dissipation.[77] They maintain stable friction coefficients across a wide temperature range and show enhanced resistance to environmental factors like salt and water exposure.[77] However, ceramic pads provide less initial "bite" or aggressive stopping power than semi-metallic pads, necessitating greater pedal pressure in scenarios requiring rapid deceleration, such as towing or emergency stops.[77] Their performance diminishes in extremely cold climates, where friction buildup is slower, and they generate higher overall system temperatures due to lower heat absorption capacity.[77] Additionally, when paired with standard rotors, they can accelerate rotor wear if not matched with high-quality components, and their higher cost—often the most expensive friction material option—limits widespread adoption to commuter vehicles, luxury sedans, and light-duty applications like those in Mercedes-Benz or Lexus models.[77] Empirical testing indicates they excel in urban stop-and-go traffic but underperform in severe-duty or track environments compared to metallic alternatives.[77] Carbon-ceramic pads, an evolution incorporating carbon fibers embedded in a ceramic matrix, emerged from aerospace-derived technologies in the late 20th century and are optimized for high-performance automotive use, often paired with carbon-ceramic rotors.[79][80] The composite structure provides exceptional thermal conductivity and stability, resisting fade at temperatures exceeding 1000°C—far beyond the 600°C limit of cast-iron systems—while reducing unsprung vehicle weight by up to 50% relative to traditional pads and rotors.[81] This material's higher friction coefficient shortens stopping distances, with tests showing reductions of approximately 10 feet from 62 mph to 0 compared to iron equivalents, and extends pad life to 3-4 times that of standard pads, potentially lasting the vehicle's service life under normal conditions.[81] Applications include supercars like the Porsche Carrera GT (introduced in 2004 with early carbon-ceramic systems) and Formula 1-derived setups, where the pads' low thermal expansion minimizes distortion under repeated high-load braking.[82][81] Despite these benefits, carbon-ceramic pads suffer from poor low-temperature performance, requiring elevated operating temperatures for optimal friction, which can lead to glazing or reduced effectiveness in cold starts or light use.[83] Their brittleness demands careful handling to avoid cracking, and replacement costs can exceed $10,000 per axle due to specialized manufacturing involving resin powders and fiber filaments.[83][81] These pads are not suited for everyday vehicles, as their advantages manifest primarily in sustained high-speed or track scenarios, where causal factors like heat accumulation would otherwise cause fade in lesser materials.[79]Specialized High-Performance Variants
Specialized high-performance brake pad variants are formulated for extreme applications such as motorsport racing, track days, and high-speed vehicles, emphasizing high friction coefficients (typically 0.4–0.6), superior heat resistance exceeding 600°C, and minimal fade during repeated hard stops from velocities over 200 km/h. These pads prioritize aggressive bite and modulation over low noise or dust production, often deriving from motorsport compounds that extend service life by 32–50% in demanding conditions compared to standard formulations.[84][85] Sintered metal pads, composed of compressed and fused metal powders including copper, iron, and bronze, deliver consistent performance in wet and dry environments with friction coefficients around 0.50, making them prevalent in motorcycle racing, rally cars, and off-road competitions. Their porous structure enhances heat dissipation and wear resistance under high loads, though they generate more rotor wear than milder compounds.[86][87][88] Carbon-carbon composite pads, featuring carbon fiber reinforcement in a carbon matrix, excel in top-tier racing and aerospace, maintaining friction coefficients of 0.5–0.7 at temperatures from 200–300°C up to 1475°F (800°C), with low wear rates in normal regimes (0.1–0.2 coefficient). However, they exhibit low initial friction below 250°C, necessitating pre-heating for optimal engagement, and are employed in endurance racing for sustained thermal stability without oxidation below 400°C.[89][90][91][92]Manufacturing and Technology
Production Processes and Backing Components
![Performance disk brake pads illustrating friction material bonded to steel backing plate][float-right] Brake pad backing components primarily consist of a stamped steel plate that serves as the structural foundation, providing rigidity, heat dissipation, and interfaces for caliper attachment.[93] The plate is typically fabricated from low-carbon steel sheets, which are cut and stamped to form precise contours including retention ears, alignment slots, and optional noise-reduction shims or abutment clips integrated via welding or adhesive.[94] Stamping occurs in progressive dies to achieve thicknesses of 2-5 mm, ensuring compliance with OEM specifications for load-bearing capacity up to several tons during braking.[95] Corrosion resistance is enhanced through powder coating, zinc plating, or galvanization, particularly for aftermarket pads exposed to environmental factors.[96] Production processes begin with the preparation of the backing plate, which undergoes surface treatment such as cleaning and coating application to promote adhesion of the friction material.[97] Friction material formulation follows, involving precise mixing of resins (e.g., phenolic, 5-15% by weight), fibers (aramid or mineral, 10-30%), fillers (graphite or metal powders, 20-50%), and additives in industrial mixers for homogeneity, often under controlled temperatures to prevent premature curing.[98] The mixture is then preformed into a rough shape or directly applied to the backing plate. Bonding occurs via hot pressing, where the assembly is subjected to 150-200°C and pressures of 50-100 MPa for 5-20 minutes, activating the resin to form a strong mechanical and chemical interlock with the backing.[99] Curing in ovens at 150-250°C for several hours follows to fully polymerize the matrix, minimizing porosity and ensuring thermal stability up to 400-600°C.[95] Post-processing includes grinding to achieve uniform thickness (typically 10-18 mm total pad height), chamfering edges to reduce initial wear noise, and machining grooves or slots for improved cooling and debris evacuation.[97] Quality control involves dynamometer testing for friction coefficient (0.3-0.5 μ) and shear strength exceeding 10 MPa at the backing interface.[94] Advanced variants employ mechanical retention systems, such as dovetail slots or rivets in the backing plate, for high-performance applications where adhesive alone may fail under extreme loads, as seen in racing pads.[100] Steel remains dominant due to its cost-effectiveness and ductility, though aluminum or stainless steel backings appear in lightweight or corrosion-prone designs, albeit at higher expense.[96]Advancements in Friction Formulations
Modern friction formulations for brake pads emphasize environmental compliance, reduced particulate emissions, and enhanced thermal stability, replacing legacy components like copper and asbestos with alternatives that maintain or improve stopping power under diverse conditions. Regulatory pressures, including U.S. state mandates limiting copper to under 0.5% by 2021 and further reductions by 2025, have spurred innovations such as stainless steel particles and mineral fillers like wollastonite to replicate copper's thermal conductivity and friction stability without ecological harm from runoff toxicity.[101][102] Ceramic-enhanced composites, incorporating silicon carbide or alumina particles bonded with resins, have advanced since the early 2000s to minimize brake dust—often by 50-90% compared to semi-metallics—and rotor wear while providing consistent coefficients of friction (typically 0.35-0.45) across temperatures up to 600°C. These formulations prioritize adhesive over abrasive mechanisms, reducing noise and vibration, though initial claims of superiority were partly marketing-driven until validated through rig testing showing extended pad life in passenger vehicles.[103][40][104] Sustainability-focused developments integrate bio-derived fillers, such as rice husk ash or vegetable waste composites, achieving friction levels comparable to non-asbestos organic pads (μ ≈ 0.4) while lowering reliance on mined minerals; a 2024 investigation confirmed these materials sustain performance in dynamometer tests with 20-30% reduced environmental impact metrics. High-performance variants, including carbon-fiber reinforced ceramics for electric vehicles, address increased mass and regenerative braking demands by improving fade resistance—retaining 80% of initial torque after 100 stops at 300°C—through optimized fiber-resin matrices.[105][106][107] Tribological engineering, via processes like fingerprinting, enables precise substitution in copper-free NAO and low-metallic pads, ensuring stable wear rates under 0.1 mm per 1000 cycles in SAE J2522 tests, with recent formulations also incorporating conductive carbons for better manufacturability and electrostatic painting adhesion. These evolutions, documented in peer-reviewed analyses over the past 15 years, reflect causal trade-offs: higher initial costs offset by longevity gains of 20-50% in fleet applications, though real-world efficacy varies by vehicle dynamics and driving patterns.[108][109][110]Performance Evaluation
Testing Standards and Durability Metrics
Testing of brake pads involves standardized procedures to evaluate friction performance, structural integrity, and longevity under simulated operating conditions. SAE International's J840 Recommended Practice specifies equipment and methods for quantifying shear strength between the friction material and backing plate, using a double-shear test fixture to apply load until failure, ensuring adhesion withstands operational stresses exceeding 10 MPa in typical applications.[111] Similarly, SAE J2684 outlines inertia dynamometer protocols derived from FMVSS 105, conducting repeated stops from speeds up to 100 km/h to assess hydraulic brake system response, including pad contribution to deceleration rates above 5 m/s² without excessive fade.[112] In Europe, UNECE Regulation 90 (ECE R90) mandates type-approval testing for replacement pads, requiring dynamometer evaluations of braking efficiency, comparing replacement linings to original equipment under type-0 (cold performance) and type-I (hot performance with fade recovery) tests, with minimum efficiency thresholds of 60-70% for light vehicles.[113] These procedures incorporate speed-load cycles simulating urban and highway use, measuring torque output to verify consistent friction over 200+ stops. Durability metrics focus on quantifiable indicators of sustained performance. The coefficient of friction (COF, μ) is a primary metric, targeted at 0.35-0.45 for standard passenger vehicle pads, tested via pin-on-disc or full-scale dynamometers under loads of 1-4 MPa and temperatures from 50°C to 500°C to ensure stability without drop below 0.3 during fade.[114] Wear rate, often calculated as specific wear rate (SWR) in mm³/Nm or mass loss per distance (e.g., <5 mg/m for low-wear formulations), employs Archard's equation—V = k * (F * L)/H, where V is volume loss, k is wear coefficient, F is force, L is sliding distance, and H is hardness—to predict pad life exceeding 30,000-50,000 km under average duty cycles.[115] [116] Additional metrics include thermal capacity, gauged by maximum operating temperature (typically 400-650°C for semi-metallic pads) before μ degradation exceeds 20%, and noise/vibration propensity via subjective and accelerometer-based assessments during modulated braking.[117] Shear strength thresholds, per SAE J840, must surpass 2.5 MPa to prevent delamination, with post-test microscopy verifying material integrity.[118] These metrics collectively ensure pads meet FMVSS 135 requirements for vehicle stopping distances under 70-80 m from 100 km/h on dry pavement, prioritizing empirical validation over manufacturer claims.[119]Comparative Effectiveness Across Conditions
Semi-metallic brake pads excel in wet conditions due to their metal content, which provides a higher coefficient of friction (typically 0.4-0.6) that resists the lubricating effect of water films on the pad-disc interface, resulting in shorter stopping distances compared to organic pads.[120][121] Organic pads, reliant on resin binders, absorb moisture more readily, leading to friction degradation and increased stopping distances by up to 20-30% in simulated wet tests.[122] Ceramic pads perform reliably in wet environments with low water absorption, maintaining friction levels close to dry conditions, though they may exhibit slightly softer initial response than semi-metallics.[123][3] In high-temperature scenarios, such as downhill descents or track use where interface temperatures exceed 400°C, semi-metallic pads demonstrate superior fade resistance owing to their conductive metal particles, sustaining friction coefficients above 0.35 even under thermal stress.[124][125] Ceramic pads offer stable performance across a broad temperature range (up to approximately 500°C) but can experience reduced effectiveness in prolonged extreme heat due to lower thermal conductivity compared to semi-metallics.[3][126] Organic pads suffer significant fade at elevated temperatures, with friction dropping below 0.3 as resins soften, necessitating avoidance in high-heat applications.[127] Under low-temperature conditions (below 0°C), organic pads provide strong initial bite from their compliant resin matrix, achieving quick friction buildup without bedding-in delays.[122] Semi-metallic pads also respond well in cold weather, benefiting from metal fibers for consistent torque.[125] Ceramic pads, however, often require a brief warm-up period to reach optimal friction, potentially extending stopping distances by 10-15% immediately after cold starts.[126][128]| Condition | Organic/NAO Effectiveness | Semi-Metallic Effectiveness | Ceramic Effectiveness |
|---|---|---|---|
| Dry | Adequate friction; prone to quicker wear | High stopping power; durable | Consistent; low noise |
| Wet | Reduced grip; longer stops | Strong resistance to water | Reliable; minimal absorption |
| High Temperature | Prone to fade; resin degradation | Excellent fade resistance | Stable but limited in extremes |
| Low Temperature | Good cold bite | Responsive | Slower initial buildup |
