The Armoloy Corporation is an innovative, US-based metal finishing company specializing in thin dense chrome and coatings application engineering. This franchising organization is equipped with an in-house metallurgical and chemical testing laboratory that focuses on the research and development of new coating technologies and applications.
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The Armoloy Corporation helps Improve metal surface performance to its highest pinnacle. Whether you’re already a partner or interested in learning more about us, we’re here to help answer any questions you may have. View a list of some of the most common questions we receive below.
- Heat Treatment: Processes like hardening, annealing, tempering, and quenching alter the internal structure of the metal to enhance properties like hardness and ductility.
- Surface Coating and Plating: Techniques such as electroplating, thermal spraying, and vapor deposition apply a protective or functional coating to the metal surface. These treatments are often used to improve corrosion resistance or wear resistance.
- Chemical Treatments: Methods like carburizing or nitriding involve adding elements like carbon or nitrogen to the surface of metals to change their surface composition, improving hardness and fatigue resistance.
The Armoloy Corporation performs all chemical, mechanical, and corrosion testing in our in-house laboratory. Armoloy also partners with 3rd party laboratories for additional testing methods when necessary.
Ball and rolling bearing components coated with Armoloy thin dense chrome
- Enhanced Hardness: Significantly increases surface hardness and wear resistance.
- Low Friction: Reduces friction, improving the efficiency and lifespan of components.
- Thermal Conductivity: Offers high thermal conductivity for better heat dissipation.
- Corrosion Resistance: Provides excellent protection against corrosion.
- Surface Uniformity: Results in a smooth, uniform surface with tight dimensional tolerances.
- Stainless Steels in Chloride Environments: SCC is most likely to occur between 50°C and 150°C (122°F to 302°F). This temperature range provides optimal conditions for chloride-induced cracking.
- Carbon Steels in Caustic Environments: SCC can occur at temperatures above 60°C (140°F), especially in concentrated caustic solutions.
- Brass in Ammonia Environments: SCC is known to occur at room temperature to slightly elevated temperatures when exposed to ammonia or ammonium compounds.
- High-Strength Alloys: SCC in high-strength alloys, such as certain aluminum or titanium alloys, can occur over a wide range of temperatures, depending on the environment and stress levels.
- Surface Roughness: Rough metal surfaces have higher friction compared to smooth, polished surfaces.
- Lubrication: Applying lubricants can reduce friction between metal surfaces. Low friction coatings like thin dense chrome can reduce friction significantly, especially when combined with the appropriate lubricant.
- Material Pairing: The combination of different metals or metal with non-metal materials can affect friction levels. For instance, metal-on-metal contact typically has higher friction compared to metal-on-plastic contact.
- Environmental Factors: Temperature, humidity, and the presence of contaminants can influence the frictional behavior of metals.
- Surface Finish: Rough or untreated steel surfaces tend to have higher friction compared to polished or smooth surfaces.
- Lubrication: Applying lubricants like oil or grease can significantly reduce the friction of steel surfaces.
- Material Interaction: The friction level of steel changes when paired with different materials. For instance, steel-on-steel contact usually has higher friction than steel-on-plastic.
- Environmental Conditions: Factors like temperature, humidity, and the presence of contaminants can also influence steel's frictional properties.
- Material Selection: Use metals that are close together on the galvanic series to minimize potential differences. Avoid combining metals with significantly different electrochemical potentials.
- Insulation: Electrically insulate dissimilar metals to prevent direct contact. Use non-conductive materials such as plastic or rubber gaskets, washers, or coatings.
- Protective Coatings: Apply protective coatings to the more noble (cathodic) metal to prevent it from acting as the cathode. Use paints, varnishes, or powder coatings to isolate the metals from the environment.
- Cathodic Protection: Implement cathodic protection systems, such as sacrificial anodes (e.g., zinc or magnesium) that corrode preferentially, protecting the primary metal.
- Control Environment: Reduce the presence of electrolytes (such as moisture or salts) that facilitate galvanic corrosion. Use dehumidifiers, sealants, and corrosion inhibitors.
- Regular Maintenance: Conduct regular inspections and maintenance to identify early signs of galvanic corrosion and address them promptly.
- Design Modifications: Redesign assemblies to avoid galvanic coupling, such as by ensuring proper drainage to avoid electrolyte accumulation and avoiding crevices where moisture can collect.
- Alloy Selection: Choose alloys with higher PREN values like 316 stainless steel for better resistance.
- Design Practices: Optimize designs to minimize crevices and promote proper drainage to reduce stagnation.
- Barrier Coatings: Use coatings like paints, epoxies, or Armoloy to protect metal surfaces from corrosive environments.
- Conduct regular inspections to detect early signs of pitting corrosion.
- Apply corrosion inhibitors to protect susceptible metals.
- Ensure proper drainage and avoid stagnant water or corrosive deposits.
- Visual Inspection: Look for characteristic signs such as:
- Surface Roughness: Increased surface roughness with grooves or pits.
- Localized Damage: Distinct localized areas where material loss is evident, often downstream or at bends.
- Surface Patterns: Patterns indicating fluid flow direction, such as streaks or scalloped surfaces.
- Non-Destructive Testing (NDT): Utilize techniques to detect subsurface damage and measure material thickness:
- Ultrasonic Testing: Measures the thickness of the material to identify areas of significant loss.
- Eddy Current Testing: Detects surface and near-surface cracks and pits.
- Radiography: Provides detailed images of the internal structure to detect erosion and corrosion.
- Chemical Analysis: Perform tests to identify the presence of corrosive agents in the environment, such as chlorides, sulfur compounds, or acids.
- Flow Analysis: Analyze the fluid dynamics in the system to identify high-velocity areas, turbulence, or impingement zones that could lead to erosion corrosion.
- Microscopic Examination: Use microscopes to examine the microstructure of the material for signs of combined mechanical and chemical wear.
- Material Composition: The inherent properties of the material, such as the type of polymer in plastics or the alloy composition in metals, determine its resistance to certain chemicals.
- Surface Treatments and Coatings: Applying protective layers that prevent chemicals from reaching the base material.
- Cross-Linking in Polymers: In polymer materials, higher degrees of cross-linking can enhance resistance to chemical attack by making the structure more stable and less permeable.
- Barrier Properties: The ability of a material to act as a barrier to chemical diffusion, preventing or slowing the penetration of aggressive substances.
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- Finite element analysis
- Thermal analysis
- Computational fluid dynamics
Where Are PFAS Found?
PFAS can be found in:
- Non-stick cookware
- Water-repellent fabrics
- Food packaging
- Firefighting foams
- Industrial processes, including chrome plating for mist suppression
Why Are PFAS a Concern?
PFAS have been linked to:
- Environmental contamination of water, soil, and air
- Accumulation in humans and wildlife
- Potential health risks, including hormonal disruptions, immune system effects, and certain cancers
- Hard Particles: Particles such as dust, sand, or debris in the environment can become trapped between surfaces and cause abrasion. These particles act like cutting tools, removing material from the softer surface.
- Surface Roughness: Rough or uneven surfaces with protrusions can abrade softer materials during contact. Smoother surfaces reduce the likelihood of abrasive wear.
- Contact Pressure: Higher contact pressures increase the abrasive action between surfaces. Maintaining optimal pressure levels can help minimize wear.
- Material Hardness: The hardness difference between contacting materials significantly affects abrasive wear. Softer materials are more susceptible to abrasion by harder counterparts.
- Environment: Harsh environments with high levels of particulate matter, such as mining or construction sites, are prone to abrasive wear. Proper sealing and protective measures can reduce exposure to these conditions.
- Lubrication: Inadequate or improper lubrication can lead to increased friction and abrasion. Using the right type of lubricant and ensuring regular maintenance can help mitigate this issue.
- Air Filtration: Installing advanced air filtration systems to remove particles before they enter the engine.
- Coatings: Applying wear-resistant coatings to the turbine blades to enhance their durability.
- Regular Maintenance: Conducting regular inspections and maintenance to identify early signs of wear and address them promptly.
- Use of Lubricants: Applying appropriate lubricants to reduce friction and wear.
- Surface Treatments: Employing surface coatings or treatments to increase hardness and resistance to fretting.
- Design Modifications: Improving joint design to minimize relative motion and increase contact stability.
- Protective Coatings: Applying erosion-resistant coatings to the rotor blades to enhance their durability against particle impacts.
- Design Modifications: Incorporating design features that reduce the impact angle and velocity of particles on critical surfaces.
- Regular Inspections: Conducting routine inspections and maintenance to detect early signs of erosion and repair damaged areas promptly.
- Chemical Agents: Exposure to corrosive substances such as acids, alkalis, salts, and oxidizing agents can initiate chemical reactions on the material surface. These reactions degrade the material, making it more susceptible to wear.
- Mechanical Stress: Mechanical actions like abrasion, erosion, or friction accelerate the removal of the chemically weakened surface layer. This exposes fresh material to further chemical attack, perpetuating the cycle of wear.
- Environmental Conditions: Harsh environments, including high humidity, temperature extremes, and the presence of corrosive gases, can exacerbate corrosive wear. For example, marine environments with saltwater are particularly aggressive.
- Material Properties: Materials with low corrosion resistance or poor mechanical strength are more prone to corrosive wear. The selection of appropriate materials is crucial to prevent rapid degradation.
- Contaminants: The presence of contaminants, such as dirt or abrasive particles, can enhance both corrosion and mechanical wear. These particles can embed in surfaces and act as sites for corrosive attack.
- Electrochemical Factors: In some cases, electrochemical reactions, such as galvanic corrosion, can occur when two dissimilar metals are in contact in the presence of an electrolyte. This can lead to accelerated corrosive wear.
- Solid Particle Erosion: Caused by the impact of solid particles, such as sand or dust, suspended in a fluid stream.
- Liquid Droplet Erosion: Occurs when high-velocity liquid droplets, often found in steam or water jets, strike a surface.
- Cavitation Erosion: Caused by the formation and collapse of vapor bubbles in a liquid, generating shock waves that erode the surface.
- Particle Characteristics: Size, shape, hardness, and velocity of impacting particles affect the wear rate.
- Impact Angle: The angle at which particles strike the surface influences the erosion mechanism. For example, shallow angles tend to cause more abrasive wear, while perpendicular impacts lead to more deformation.
- Material Properties: The hardness, toughness, and ductility of the material determine its resistance to erosive wear.
- High Contact Stresses: The interaction between the wheel and rail generates high contact stresses at the gauge corner, leading to material fatigue and crack initiation.
- Rolling Contact Fatigue: Repetitive rolling contact under high loads causes micro-cracks to form and propagate in the rail material.
- Friction and Slip: The relative motion between the wheel and rail, especially during curves or braking, induces additional shear stresses and contributes to crack growth.
- Material Properties: Rail steel composition and microstructure play a critical role in susceptibility to GCC. Harder rail materials may resist wear but can be more prone to cracking under cyclic loading.
- Environmental Factors: Temperature variations, moisture, and contamination can exacerbate the development and propagation of cracks.
- Regular Inspections: Conducting frequent inspections using non-destructive testing methods, such as ultrasonic or eddy current testing, to detect early signs of GCC.
- Rail Grinding: Periodic rail grinding to remove surface defects and maintain optimal rail profile, reducing stress concentrations.
- Lubrication: Applying rail lubricants or friction modifiers to minimize friction and wear at the gauge corner.
- Material Improvements: Utilizing advanced rail steels with improved resistance to fatigue and cracking.
- Durability: The material remains physically and chemically stable over time when exposed to chemicals.
- Minimal Swelling or Degradation: The material does not absorb chemicals or swell excessively, which can lead to loss of mechanical integrity.
- Retention of Mechanical Properties: The material retains its strength, flexibility, and other mechanical properties after chemical exposure.
- Low Permeability: The material does not allow chemicals to pass through easily, maintaining a barrier to protect underlying surfaces or structures.
- Plating and Coating: Electroplating or chemical processes create a protective metal coating, such as thin dense chrome or electroless nickel, on the mold. These coatings are primarily chosen for corrosion and wear resistance.
- Chemical Vapor Deposition (CVD): CVD coatings, such as silicon carbide or boron nitride, are chemically reactive layers that enhance the mold's hardness and resistance to wear and heat.
- Physical Vapor Deposition (PVD): PVD forms a thin film on the mold using materials like TiN or TiCN. These coatings increase hardness and protect the mold from wear and abrasion.
- Oxidation Treatment: This method creates an oxide layer on the mold surface to increase corrosion resistance and surface hardness. Common techniques include anodizing and phosphating.
- Thermal Spray: This technique uses a spray gun to apply melted metal or alloy materials, such as ceramics, carbide, or metals. It forms a hard, wear-resistant layer that improves mold durability.
- Polymers: Polymer coatings like polyether or polyurethane are applied to molds to provide excellent wear and corrosion resistance.
- Mechanical Interlocking Theory: This theory posits that adhesion occurs when the adhesive penetrates the pores and irregularities of the substrate, creating a mechanical bond. This interlocking effect enhances the adhesive strength by anchoring the adhesive to the surface.
- Electrostatic Theory: According to this theory, adhesion results from electrostatic forces between the adhesive and the substrate. When two surfaces come into contact, an electrical double layer forms, generating electrostatic attraction that contributes to the adhesive bond.
- Diffusion Theory: This theory suggests that adhesion is due to the interdiffusion of molecules at the interface of the adhesive and the substrate. When materials with similar molecular structures come into contact, their molecules intermix, creating a strong adhesive bond through molecular entanglement.
- Chemical Bonding Theory: This theory states that adhesion is caused by the formation of chemical bonds (such as covalent, ionic, or hydrogen bonds) between the adhesive and the substrate. These bonds result from chemical reactions at the interface, providing strong adhesion.
- Level 1: Submission of the Part Submission Warrant (PSW) only.
- Level 2: PSW with product samples and limited supporting data.
- Level 3: PSW with product samples and complete supporting data (the most commonly required level).
- Level 4: PSW and other requirements as defined by the customer.
- Level 5: PSW with product samples and complete data, including an on-site review at the supplier's manufacturing location.
- Galling: This occurs when severe adhesive wear causes the surfaces to seize and weld together. It results in significant material transfer and surface damage, leading to operational failure.
- Scoring: Visible grooves or scratches appear on the surface due to repeated adhesive contact. This type of failure can reduce the efficiency of sliding components and increase friction.
- Seizing: The surfaces lock together due to strong adhesive forces, often leading to a sudden and complete failure of the component. This can halt machinery operations and cause extensive damage.
- Material Transfer: Particles from one surface transfer to another, leading to uneven wear and potential imbalance in rotating machinery. This can cause vibrations and reduced precision in operations.
- Surface Fatigue: Repeated adhesive contact can lead to surface fatigue, characterized by the initiation and growth of cracks. Over time, this results in the spalling or flaking of material.
- Pitting: Small pits or craters form on the surface due to localized adhesive failure. This can compromise the structural integrity of components and lead to premature failure.
- PTFE (Polytetrafluoroethylene): Known widely as Teflon®, used in non-stick cookware and industrial applications.
- FEP (Fluorinated Ethylene Propylene): Used in wire insulation and chemical processing equipment.
- PFA (Perfluoroalkoxy Alkane): Known for its high temperature and chemical resistance, used in semiconductor manufacturing.
- ETFE (Ethylene Tetrafluoroethylene): Used in architectural applications for its durability and resistance to weathering.
- PVDF (Polyvinylidene Fluoride): Used in the chemical industry for its resistance to solvents and acids.
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- Abrasive Wear: Occurs when hard particles or hard protuberances on a surface slide or roll across a softer surface, causing material removal. It is common in environments with high levels of dust or particulates.
- Adhesive Wear: Happens when two solid surfaces slide over each other, causing material transfer from one surface to another. This type of wear is often seen in metal-to-metal contact and can result in galling or seizing.
- Corrosive Wear: Combines chemical reactions with mechanical wear. Corrosive substances, such as acids or alkalis, degrade the material's surface, which then wears away more easily when subjected to mechanical action.
- Fatigue Wear: Caused by repeated loading and unloading cycles that lead to the formation of cracks and material flaking. This type of wear is prevalent in components subject to cyclic stresses, like bearings and gears.
- Tensile Stress: The presence of tensile stress, either applied or residual, is essential for SCC. This stress can result from mechanical loads, thermal cycles, or welding processes.
- Corrosive Environment: A specific corrosive environment is necessary to initiate and propagate SCC. Common environments include chlorides for stainless steels, caustic solutions for carbon steels, and ammonia for brass.
- Susceptible Material: The material must be susceptible to SCC in the given environment. Factors such as alloy composition, microstructure, and heat treatment can influence susceptibility.
- Stress Relief: Reduce residual stresses through heat treatment, annealing, or stress-relief processes.
- Environmental Control: Minimize exposure to specific corrosive agents known to cause SCC for the material in use.
- Material Selection: Use materials with higher resistance to SCC in the intended service environment.
- Relative Motion: Micro-movements or vibrations between contact surfaces, typically in the range of micrometers to millimeters, lead to repeated contact and separation.
- High Contact Pressure: Increased contact pressure intensifies the frictional forces and wear between the surfaces.
- Environmental Conditions: Presence of oxygen and humidity can exacerbate fretting by forming abrasive oxide particles (fretting corrosion).
- Material Properties: Softer materials are more susceptible to fretting wear, and the presence of hard particles can act as abrasives.
- Surface Roughness: Rough surfaces increase the likelihood of asperity interactions, leading to higher wear rates.
- Cyclic Loading: Components subjected to cyclic or oscillatory loads, such as vibrations or thermal cycling, are more prone to fretting.
- Bolted Joints: Slight movements in bolted joints due to dynamic loading.
- Bearings: Micro-movements between bearing surfaces under load.
- Electrical Contacts: Vibrations in electrical connectors leading to fretting corrosion.
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