Hubbry Logo
Polyamide-imidePolyamide-imideMain
Open search
Polyamide-imide
Community hub
Polyamide-imide
logo
7 pages, 0 posts
0 subscribers
Be the first to start a discussion here.
Be the first to start a discussion here.
Polyamide-imide
Polyamide-imide
Polyamide-imide
View on Wikipedia
from Wikipedia

Polyamide-imides are either thermosetting or thermoplastic, amorphous polymers that have exceptional mechanical, thermal and chemical resistant properties. Polyamide-imides are used extensively as wire coatings in making magnet wire. They are prepared from isocyanates and TMA (trimellic acid-anhydride) in N-methyl-2-pyrrolidone (NMP). A prominent distributor of polyamide-imides is Solvay Specialty Polymers, which uses the trademark Torlon.

Polyamide-imides display a combination of properties from both polyamides and polyimides, such as high strength, melt processibility,[clarification needed] exceptional high heat capability, and broad chemical resistance.[citation needed] Polyamide-imide polymers can be processed into a wide variety of forms, from injection or compression molded parts and ingots, to coatings, films, fibers and adhesives. Generally these articles reach their maximum properties with a subsequent thermal cure process.

Other high-performance polymers in this same realm are polyetheretherketones and polyimides.

Chemistry

[edit]

The currently popular commercial methods to synthesize polyamide-imides are the acid chloride route and the isocyanate route.

Acid chloride route

[edit]
Trimellitic acid chloride
Methylene dianiline

The earliest route to polyamide-imides is the condensation of an aromatic diamine, such as methylene dianiline (MDA) and trimellitic acid chloride (TMAC). Reaction of the anhydride with the diamine produces an intermediate amic acid. The acid chloride functionality reacts with the aromatic amine to give the amide bond and hydrochloric acid (HCl) as a by-product. In the commercial preparation of polyamideimides, the polymerization is carried out in a dipolar, aprotic solvent such as N-methylpyrrolidone (NMP), dimethylacetamide (DMAC), dimethylformamide (DMF), or dimethylsulfoxide (DMSO) at temperatures between 20 and 60 °C (68 and 140 °F). The byproduct HCl must be neutralized in situ or removed by washing it from the precipitated polymer. Further thermal treatment of the polyamideimide polymer increases molecular weight and causes the amic acid groups to form imides with the evolution of water.

Diisocyanate route

[edit]

This is the primary route to polyamide-imides which are used as wire enamels. A diisocyanate, often 4,4’-methylenediphenyldiisocyanate (MDI), is reacted with trimellitic anhydride (TMA). The product achieved at the end of this process is a high molecular weight, fully imidized polymer solution with no condensation byproducts, since the carbon dioxide gas byproduct is easily removed. This form is convenient for the manufacture of wire enamel or coatings. The solution viscosity is controlled by stoichiometry, monofunctional reagents, and polymer solids. The typical polymer solids level is 35-45% and it may be diluted further by the supplier or user with diluents.

Fabrication

[edit]

Polyamide-imides are commercially used for coatings and molded articles.

Coatings

[edit]

The product used mainly for coatings is sold in a powdered form and is roughly 50% imidized. One of the major uses is as a magnet wire enamel. The magnet wire enamel is made by dissolving the PAI powder in a strong, aprotic solvent such as N-methyl pyrrolidone. Diluents and other additives can be added to provide the correct viscosity for application to the copper or aluminum conductor. Application is typically done by drawing the conductor through a bath of enamel and then through a die to control coating thickness. The wire is then passed through an oven to drive off the solvent and cure the coating. The wire usually is passed through the process several times to achieve the desired coating thickness.

The PAI enamel is very thermally stable as well as abrasion and chemical resistant. PAI is often used over polyester wire enamels to achieve higher thermal ratings.

PAI is also used in decorative, corrosion resistant coatings for industrial uses, often in conjunction with fluoropolymers. The PAI aids in adhering the fluoropolymer to the metal substrate. They also find usage in non-stick cookware coatings. While solvents can be used, some water-borne systems are used. These are possible because the amide-imide contains acid functionality.

Molded or machined articles

[edit]

The polyamide-imides used for molded articles are also based on aromatic diamines and trimellitic acid chloride, but the diamines are different from those used in the products used for coatings and the polymer is more fully imidized prior to compounding and pelletizing. Resins for injection molding include unreinforced, glass-fiber reinforced, carbon fiber reinforced, and wear resistant grades. These resins are sold at a relatively low molecular weight so they can be melt processed by extrusion or injection-molding. The molded articles are then thermally treated for several days at temperatures up to 260 °C (500 °F). During this treatment, commonly referred to a postcure, the molecular weight increases through chain extension and the polymer gets much stronger and more chemically resistant. Prior to postcure, parts can be reground and reprocessed. After postcure, reprocessing is not practical.

Properties of molded PAI

[edit]
Property Test method Units Molded PAI
Tensile strength, ultimate ASTM D 638 MPa, average value 91.6
Tensile modulus ASTM D 638 GPa, average value 3.97
Tensile elongation ASTM D 638 % 3.15
Flexural strength ASTM D 790 MPa 133
Flexural modulus ASTM D 638 GPa 4.58
Compressive strength ASTM D 695 MPa, average 132
Izod impact strength ASTM D 256 J/m (ft-lb/in) average 0.521 (1)
Heat deflection temperature @ 264 psi ASTM D 648 °C (°F) 273 (523)
Coefficient of linear thermal expansion ASTM D 696 ppm/°C 37.7
Volume resistivity ASTM D 257 ohm-cm, average 8.10×1012
Density ASTM D 792 g/cm3 1.48
Water absorption, 24 hr ASTM D 570 % 0.35

High-strength grades only

[edit]
Property Test method Units Neat PAI 30% GF PAI 30% CF PAI
Tensile strength ASTM D 638 MPa (kpsi) 152 (22.0) 221 (32.1) 221 (32.0)
Tensile modulus ASTM D 638 GPa (kpsi) 4.5 (650) 14.5 (2,110) 16.5 (2,400)
Tensile elongation ASTM D 638 % 7.6 2.3 1.5
Flexural strength ASTM D 790 MPa (kpsi) 241 (34.9) 333 (48.3) 350 (50.7)
Flexural modulus ASTM D 790 GPa (kpsi) 5.0 (730) 11.7 (1,700) 16.5 (2,400)
Compressive strength ASTM D 695 MPa (kpsi) 221 (32.1) 264 (38.3) 254 (36.9)
Shear strength ASTM D 732 MPa (kpsi) 128 (18.5) 139 (20.1) 119 (17.3)
Izod impact strength ASTM D 256 J/m (ftlb/in) 144 (2.7) 80 (1.5) 48 (0.9)
Izod impact strength, unnotched ASTM D 4812 J/m (ftlb/in) 1070 (20) 530 (10) 320 (6)
Heat deflection temperature @ 264 psi ASTM D 648 °C (°F) 278 (532) 282 (540) 282 (540)
Coefficient linear thermal Expansion ASTM D 696 ppm/°C (ppm/°F) 31 (17) 16 (9) 9 (5)
Volume resistivity ASTM D 257 ohm-cm 2e17 2e17
Specific gravity ASTM D 792 1.42 1.61 1.48
Water absorption, 24 hr ASTM D 570 % 0.33 0.24 0.26

Wear-resistant PAI grades

[edit]
Property Test method Units 4275 4301 4435 4630 4645
Tensile strength ASTM D 638 MPa (kpsi) 117 (16.9) 113 (16.4) 94 (13.6) 81 (11.8) 114 (16.6)
Tensile modulus ASTM D 638 GPa (kpsi) 8.8 (1,280) 6.8 (990) 14.5 (2,100) 7.4 (1,080) 18.6 (2,700)
Tensile elongation ASTM D 638 % 2.6 3.3 1.0 1.9 0.8
Flexural strength ASTM D 790 MPa (kpsi) 208 (30.2) 215 (31.2) 152 (22.0) 131 (19.0) 154 (22.4)
Flexural modulus ASTM D 790 GPa (kpsi) 7.3 (1.060) 6.9 (1,000) 14.8 (2,150) 6.8 (990) 12.4 (1,800)
Compressive strength ASTM D 695 MPa (kpsi) 123 (17.8) 166 (24.1) 138 (20.0) 99 (14.4) 157 (22.8)
Izod impact strength, notched ASTM D 256 J/m (ft-lb/in) 85 (1.6) 64 (1.2) 43 (0.8) 48 (0.9) 37 (0.7)
Izod impact strength, unnotched ASTM D 4812 J/m (ft-lb/in) 270 (5) 430 (8) 210 (4) 160 (3) 110 (2)
Heat deflection temperature at 264 psi ASTM D 648 °C (°F) 280 (536) 279 (534) 278 (532) 280 (536) 281 (538)
Coefficient linear thermal expansion ASTM D 696 ppm/°C (ppm/°F) 25 (14) 25 (14) 14 (8) 16 (9) 9 (3)

Injection molding

[edit]

Polyamide-imide resin is hygroscopic, and picks up ambient moisture. Before processing the resin, drying is required to avoid brittle parts, foaming, and other molding problems. The resin must be dried to a moisture content of 500 ppm or less. A desiccant dryer capable of maintaining a dew point of −40 °F (−40 °C) is recommended. If drying is done in pans or trays, put the resin in layers no more than 2 to 3 inches (5.1 to 7.6 centimetres) deep in drying trays. Dry for 24 hours at 250 °F (121 °C), 16 hours at 300 °F (149 °C), or 8 hours at 350 °F (177 °C). If drying at 350 °F, limit drying time to 16 hours. For the injection molding press, a desiccant hopper dryer is recommended. The circulating air suction pipe should be at the base of the hopper, as near the feed throat as possible.

In general, modern reciprocating-screw injection molding presses with microprocessor controls capable of closed-loop control are recommended for molding PAI. The press should be fitted with a low compression ratio, constant taper screw. The compression ratio should be between 1.1 and 1.5 to 1, and no check device should be used. The starting mold temperatures are specified as follows:[citation needed]

Zone Temp, °F Temp, °C
Feed zone 580 304
Middle zone 620 327
Front zone 650 343
Nozzle 700 371

The mold temperature should be in the range of 325 to 425 °F (163 to 218 °C).

Other applications

[edit]

The high temperature and chemical resistance of polyamide-imides make them in principle suitable for membrane based gas separations. The separation of contaminants such as CO2, H2S, and other impurities from natural gas wells is an important industrial process. Pressures exceeding 1000 psia demand materials with good mechanical stability. The highly polar H2S and polarizable CO2 molecules can strongly interact with the polymer membranes causing swelling and plasticization[1] due to high levels of impurities. Polyamide-imides can resist plasticization because of the strong intermolecular interactions arising from the polyimide functions as well as the ability of the polymer chains to hydrogen bond with one another as a result of the amide bond. Although not currently used in any major industrial separation, polyamide-imides could be used for these types of processes where chemical and mechanical stability are required.

See also

[edit]

References

[edit]

Further reading

[edit]
Revisions and contributorsEdit on WikipediaRead on Wikipedia

Polyamide-imide

View on Grokipedia
from Grokipedia
Polyamide-imide (PAI) is an amorphous characterized by a molecular structure incorporating both (-CONH-) and (-CO-NR-CO-, where R is typically an aromatic group) linkages, typically derived from aromatic monomers, which confer exceptional thermal stability, mechanical strength, and chemical resistance. This high-performance material exhibits a temperature (T_g) exceeding 275°C, allowing it to maintain structural integrity and mechanical properties from cryogenic temperatures up to approximately 260°C in continuous use. Developed initially at in the mid-1950s and commercialized by Chemicals in the early 1960s under the Torlon, PAI represents one of the earliest high-performance thermoplastics, now produced by Syensqo (formerly Solvay). Its synthesis typically involves condensation polymerization of trimellitic anhydride with aromatic diamines or diisocyanates, followed by processing via injection molding or , often requiring post-curing at elevated temperatures to optimize properties. PAI demonstrates superior —twice that of many other thermoplastics like PEEK—along with excellent wear resistance, low coefficient of , and resistance to most chemicals except strong alkalis and oxidizing acids. In fire-prone environments, it offers low heat release rates, high ignition temperatures around 643°C, and significant char formation for enhanced safety. The material's defining applications span demanding sectors such as (e.g., hardware and seals), automotive (e.g., transmission components and bearings), oil and gas (e.g., valves and compressors), and (e.g., insulation and parts), where its ability to outperform metals in weight-sensitive, high-stress conditions is particularly valued. Additionally, PAI finds use in nuclear reactors due to its stability and in medical devices for its and sterilizability. Despite processing challenges like moisture sensitivity and the need for specialized equipment, ongoing advancements in nanocomposites and formulations continue to expand its utility in advanced solutions.

Overview

Definition and Classification

Polyamide-imide (PAI) is a class of high-performance, amorphous polymers characterized by the presence of both (-CONH-) and (-CONCO-) linkages in their molecular backbone, which imparts a hybrid structure combining the attributes of polyamides and polyimides. This hybrid nature allows PAI to exhibit enhanced thermal and mechanical properties compared to conventional polyamides, while maintaining better processability than fully aromatic polyimides. The term "polyamide-imide" directly reflects this combined , denoting polymers that incorporate repeating units of both functional groups. PAI polymers are primarily classified as thermoplastics, which are melt-processable and can be shaped via injection molding or , as exemplified by commercial grades like Torlon PAI. However, certain variants exist as thermosets, which during to form insoluble networks with heightened durability in extreme conditions. In distinction from pure , which lack groups and thus offer lower resistance, and , which are devoid of linkages and often require complex high-temperature , PAI occupies a unique position within the broader family of - and -based polymers. Key characteristics of PAI include high thermal stability suitable for continuous use up to 260°C, exceptional mechanical strength that rivals metals in demanding applications, and broad chemical inertness to acids, hydrocarbons, and solvents. These properties position PAI as a versatile material in high-performance contexts, bridging the gap between the flexibility of polyamides and the rigidity of polyimides without requiring the specialized synthesis routes typical of the latter.

History and Commercial Development

The development of polyamide-imide (PAI) polymers began in the mid-1950s at , where initial research focused on high-performance materials with linkages for enhanced stability. By the early 1960s, of (later Amoco Chemicals, now Syensqo, formerly Solvay) advanced the technology, securing key patents around 1960 for synthesis routes involving -amic acid derived from trimellitic anhydride and diamines. These allowed for the formation of soluble polymers that could be processed and then cyclized to yield robust PAI structures, marking a pivotal shift toward practical industrial applications. A major milestone occurred in the early 1960s when Chemicals commercialized Torlon PAI, the first melt-processable variant of the polymer, enabling injection molding and for demanding environments. This introduction addressed previous limitations in processability while retaining superior mechanical and thermal properties, positioning PAI as a leader among engineering thermoplastics. During the , PAI production expanded significantly for components, driven by its ability to withstand extreme temperatures and stresses in aircraft bearings, seals, and structural parts. Post-2000 advancements have further diversified PAI's role, particularly in high-performance composites reinforced with fibers for automotive and industrial uses, and in nanofiltration membranes where its chemical resistance supports solvent-stable separations. Major commercial products include Syensqo's Torlon family, with grades such as PAI-121 (a fine for coatings) and PAI-420 (optimized for bearings with enhanced wear resistance), alongside Isomid formulations used in wire enamels by various producers. In 2023, Solvay's specialty polymers business, including Torlon PAI, was spun off to form Syensqo, continuing production and innovation. Market growth has been fueled by demand in high-temperature sectors like and oil & gas, with global production estimated at approximately 10,000-16,000 tons annually in the .

Chemistry and Synthesis

Molecular Structure

Polyamide-imide (PAI) polymers feature a backbone composed of alternating (-CONH-) and (-CON-CO-) linkages, which integrate the structural elements of polyamides and polyimides. These repeating units are typically derived from trimellitic anhydride (TMA), a tricarboxylic compound, reacted with aromatic diamines such as m-phenylenediamine or 4,4'-oxydianiline, resulting in a sequence where rings form via cyclization of adjacent groups. A representative structural formula for the repeating unit, simplified for the TMA-m-phenylenediamine system, can be depicted as: [−NH−C6H4−NH−CO−C6H3(CO)−N−]n\left[ -\mathrm{NH-C_6H_4-NH-CO-C_6H_3(CO)-N-} \right]_n where the central aromatic ring from TMA incorporates the five-membered ring fused at positions 1 and 2, with the amide linkage at position 4, and C6H4\mathrm{C_6H_4} denotes the meta-phenylene group; the notation Ar\mathrm{Ar} generally represents aromatic moieties in such chains. This hybrid architecture confers thermal rigidity from the planar, conjugated rings, which restrict chain mobility, while the flexible linkages improve and processability relative to fully imidized polyimides. Structural variations in PAI include linear chains from stoichiometric monomer ratios and branched architectures introduced via multifunctional monomers, which influence packing efficiency; the irregular placement of imide units in copolymer sequences typically renders PAI amorphous, enhancing transparency and melt processability. Spectroscopic confirmation of the molecular structure is achieved through Fourier-transform (FTIR) spectroscopy, revealing characteristic absorption peaks for imide carbonyl stretches at approximately 1780 cm⁻¹ (asymmetric) and 1715 cm⁻¹ (symmetric), alongside the amide carbonyl at around 1650 cm⁻¹.

Acid Chloride Route

The acid chloride route to polyamide-imide (PAI) synthesis involves the low-temperature solution polycondensation of trimellitic anhydride acid chloride (TMAC), derived from the phosgenation of trimellitic anhydride, with aromatic diamines such as m-phenylenediamine or 4,4'-oxydianiline in polar aprotic solvents like N-methyl-2-pyrrolidone (NMP) or N,N-dimethylacetamide (DMAc). This method forms a soluble precursor that can be processed into films, coatings, or moldings before final cyclization. The reaction mechanism proceeds via nucleophilic acyl substitution, where the primary amine groups of the attack the more reactive acid chloride moiety of TMAC, forming linkages and releasing (HCl) as a byproduct. The ortho-positioned anhydride group in TMAC remains available for subsequent intramolecular reaction, yielding an intermediate poly(amide-amic acid) with pendant and functionalities. This two-step process ensures controlled chain growth without premature gelation. Bases such as or triethylamine are often added to scavenge HCl and maintain a neutral environment, preventing side reactions like . Polymerization typically occurs at 0–25°C to manage the exothermic nature of the reaction and achieve high molecular weight precursors with intrinsic viscosities of 0.5–2.0 dL/g. The poly(amide-amic acid) intermediate then undergoes thermal imidization through and cyclization to form the characteristic five-membered rings, enhancing stability. This step is conducted by heating to 200–250°C under inert atmosphere or vacuum, often in stages (e.g., 150°C for 1 hour, then 200–250°C for 2–4 hours) to gradually remove and volatiles. The overall process yields PAIs with excellent molecular weight control and minimal branching, making it suitable for high-performance applications. Typical yields exceed 90%, with the route's advantages including economic scalability and compatibility with solution processing. The key polymerization reaction can be schematically represented as: \ce(O=C)2O−C6H3−COCl+H2N−Ar−NH2−>[0−25°C,NMP/DMAc,base][−NH−Ar−NH−CO−C6H3(COOH)−CO−]n+HCl\ce{(O=C)2O-C6H3-COCl + H2N-Ar-NH2 ->[0-25°C, NMP/DMAc, base] [-NH-Ar-NH-CO-C6H3(COOH)-CO-]_n + HCl} followed by thermal dehydration: \ce[−NH−Ar−NH−CO−C6H3(COOH)−CO−]n−>[200−250°C][−NH−Ar−NH−CO−C6H3(CO−N−CO)−]n+nH2O\ce{[-NH-Ar-NH-CO-C6H3(COOH)-CO-]_n ->[200-250°C] [-NH-Ar-NH-CO-C6H3(CO-N-CO)-]_n + n H2O} where Ar denotes the aromatic diamine backbone. This acid chloride route serves as the primary industrial process for producing Torlon PAI, a commercial thermoplastic resin known for its superior mechanical and thermal performance in demanding environments.

Diisocyanate Route

The diisocyanate route to polyamide-imide (PAI) involves the direct polycondensation of aromatic , such as 4,4'-methylenebis(phenyl ) (MDI), with trimellitic anhydride (TMA), typically conducted in polar aprotic solvents to yield soluble prepolymers suitable for thermosetting applications. This method contrasts with routes emphasizing variants by prioritizing the formation of reactive intermediates that enable easier processing into coatings. The reaction proceeds through a stepwise mechanism where the anhydride group of TMA reacts with the diisocyanate, initially forming a poly(amide-amic ) intermediate via ring-opening. Subsequent heating promotes chain extension through formation and cyclization to structures, accompanied by evolution. This can occur in a one-pot process or as a two-step treatment, with the overall simplified reaction represented as: \ceOCN−Ar−NCO+(CO)2O−C6H3−CO−>[80−140°C,NMP/DMAc][−NH−CO−Ar−NH−CO−C6H3(COOH)−CO−]n−>[250−260°C]imidizedPAI+CO2+H2O\ce{OCN-Ar-NCO + (CO)2O-C6H3-CO ->[80-140°C, NMP/DMAc] [-NH-CO-Ar-NH-CO-C6H3(COOH)-CO-]_n ->[250-260°C] imidized PAI + CO2 + H2O} where Ar denotes aromatic groups from MDI and the C6H3 from TMA. Synthesis conditions typically employ high-boiling solvents like N-methyl-2-pyrrolidone (NMP) or N,N-dimethylacetamide (DMAc) under atmosphere to prevent side reactions, with initial temperatures around 80°C for formation followed by 120–140°C for chain extension over 2 hours, achieving optimal intrinsic viscosities near a 1:1 molar ratio of MDI to TMA. While solvent-free variants exist at higher temperatures up to 210°C under , solvent-based approaches are preferred for controlling at 30% solids content; organotin catalysts may accelerate initial reactions if present, though they are not always required. This route offers advantages for thermosetting PAIs, including a simpler, faster reaction profile compared to multistep alternatives and the production of lower-viscosity prepolymers that remain soluble for application as wire enamels or coatings before final imidization and curing at 250–260°C. It is particularly suited for electrical insulation coatings on wires, where the resulting films exhibit high stability (decomposition onset >300°C) and mechanical post-cure.

Properties

Thermal Properties

Polyamide-imide (PAI) demonstrates superior thermal stability, primarily due to its incorporation of rings in the polymer backbone, which provide rigidity and resistance to degradation at high temperatures. The temperature (Tg) for unfilled PAI typically ranges from 270 to 280°C, maintaining structural integrity and high modulus even near this threshold. PAI supports continuous operational temperatures up to 260°C in air, with short-term exposure tolerance extending to 300°C without significant loss of properties. Thermal decomposition onset occurs above 500°C under inert conditions, as evidenced by (TGA) showing minimal weight loss—approximately 1% at 400°C in oxidative environments—highlighting its excellent oxidative stability. Additionally, PAI exhibits a low of linear , typically 30-50 × 10⁻⁶/°C, which contributes to dimensional stability under thermal cycling. In terms of flame retardancy, PAI achieves a UL94 V-0 rating inherently, without additives, and generates low during combustion, making it suitable for safety-critical environments. Compared to analogous polymers, PAI's Tg surpasses that of conventional polyamides (around 150°C) while falling short of fully aromatic polyimides (often exceeding 300°C), positioning it as a versatile high-performance for intermediate thermal demands.

Mechanical and Wear Properties

Polyamide-imide (PAI) exhibits exceptional mechanical strength and toughness, making it suitable for demanding load-bearing applications in molded and filled forms. Unfilled grades typically demonstrate tensile strengths ranging from 120 to 150 MPa, with elongations at break of 10-30%, providing a balance of rigidity and . High-strength grades, such as carbon-fiber reinforced variants like Torlon 7130, achieve tensile strengths up to 150 MPa or more, enhancing performance in structural components like bearings. Compressive strength exceeds 200 MPa across many grades, reflecting PAI's ability to withstand high static loads without significant deformation; for instance, glass-fiber reinforced Torlon 5030 reaches 260 MPa. The flexural modulus for unfilled and moderately filled grades falls between 4 and 6 GPa, contributing to under bending stresses, while filled variants can exceed this for specialized uses. Impact resistance, measured by notched testing, ranges from 20 to 50 J/m, with unfilled grades like Torlon 4203 showing higher values around 140 J/m due to greater elongation. Fatigue resistance under cyclic loads is notable, attributed to the polymer's inherent stability. Creep resistance remains minimal even at elevated temperatures, owing to PAI's rigid molecular backbone featuring alternating and linkages that restrict chain mobility under sustained stress. This property is particularly evident in grades like Torlon 7130, where creep strain under loads up to 103 MPa at 204°C shows negligible long-term deformation compared to other thermoplastics. Wear properties are outstanding, with PAI offering a low coefficient of friction (0.2-0.4) in dry conditions, enabling self-lubricating behavior in tribological applications. The PV limit surpasses 50,000 psi-ft/min in bearing grades, indicating high load-velocity tolerance before excessive wear occurs. These characteristics are enhanced by fillers such as and (MoS2); for example, Torlon 4301, containing approximately 15% and 3% PTFE, reduces the coefficient of friction to around 0.31 and wear factor to 28 × 10⁻⁸ mm³/N·m, making it ideal for high-wear environments like seals and bushings.
PropertyUnfilled PAI (e.g., Torlon 4203)High-Strength Grade (e.g., Torlon 7130)Wear-Resistant Grade (e.g., Torlon 4301)
Tensile Strength (MPa)120-150Up to 150+110-120
Elongation at Break (%)10-302-52-3
(MPa)>200>250>170
(GPa)4-615-206-7
Notched Impact (J/m)20-50 (up to 140)40-5050-60
Coefficient of 0.3-0.40.30.2-0.3
PV Limit (psi-ft/min)>40,000>30,000>50,000
This table summarizes representative values for molded PAI grades, highlighting how fillers tailor properties for specific mechanical and wear demands.

Chemical Resistance

Polyamide-imide (PAI) demonstrates robust chemical resistance due to its amorphous structure and linkages, which provide inherent stability against a wide range of substances, particularly at elevated temperatures up to 93°C. It remains inert to most hydrocarbons, including aliphatic and aromatic types, as well as chlorinated and fluorinated solvents, showing no significant degradation or weight change after 24-hour exposure. Weak acids and alcohols also exhibit minimal impact, with ratings of "A" (excellent) in standardized tests for substances like 10% acetic acid and 10% . However, PAI shows conditional resistance (rating "C") to polar aprotic solvents such as (DMF) at high temperatures, where swelling may occur, and poor resistance (rating "F") to strong bases like 15-30% . Hydrolysis stability is a key advantage of PAI over traditional polyamides, attributed to the protective groups that limit chain scission in aqueous environments. PAI retains over 90% of its tensile strength after prolonged immersion in , with equilibrium absorption of about 2.5% at 50% relative for unfilled grades, and it withstands more than 500 sterilization cycles at 134°C without significant property loss. Unlike polyamides prone to hydrolytic degradation, PAI exhibits reversible uptake that can be mitigated by , though it is sensitive to saturated , leading to gradual softening if not post-cured properly. In aggressive media, such as 10% NaOH at 100°C, unfilled PAI may experience weight gain or surface attack, but no measurable change occurs in 10% HCl under similar conditions. PAI offers excellent tolerance to , with negligible degradation under gamma irradiation up to 10^9 rads, resulting in only about 5% loss in tensile strength, making it suitable for nuclear and applications requiring sterilization. UV and resistance is also strong, with no observable yellowing or mechanical degradation after 6,000 hours in accelerated Weather-O-Meter testing, though prolonged outdoor exposure may cause minor surface changes due to moisture absorption. Overall, PAI maintains stability across a broad range of 2-12 in dilute solutions at moderate temperatures, but performance diminishes in concentrated alkalis. Glass-filled PAI grades preserve the base polymer's resistance to most solvents and acids but are more susceptible to leaching or reduced performance in alkaline environments, as the glass reinforcement destabilizes under bases like NaOH, potentially releasing silicates. This effect is minimal in hydrocarbons or weak acids, allowing filled variants to retain over 95% flexural strength after exposure to automotive fluids at 149°C for extended periods. In chemically aggressive settings, these grades may exhibit slightly accelerated wear compared to unfilled PAI, but they remain viable for demanding industrial uses.

Fabrication and Processing

Coatings

Polyamide-imide (PAI) coatings are applied via solution-based methods, where the polymer is dissolved in aprotic polar solvents such as N-methyl-2-pyrrolidone (NMP) or N,N-dimethylacetamide (DMAc) to form a viscous enamel or . These solutions are derived from PAI resins synthesized through routes like the diisocyanate , which yield soluble polymers suitable for direct coating without requiring a separate precursor step, though some formulations involve partial imidization during preparation. Application techniques include dip-coating for magnet wires, where the substrate is immersed in the solution and withdrawn at controlled speeds, or spray, roll, spin, and curtain methods for surface on metals and components. Following application, the coatings undergo thermal curing in ovens to evaporate solvents and achieve full imidization and chain extension, typically at 250–350°C for 1–5 minutes in continuous for wires or longer stepwise cycles (e.g., 60 minutes at 149°C, 15 minutes at 260°C, 5 minutes at 315°C) for thicker films. Coating thicknesses for wire enamels generally range from 10 to 50 μm, achieved through multiple passes to build uniform layers, while surface coatings are often 10–20 μm for optimal performance. PAI coatings exhibit exceptional exceeding 200 kV/mm, enabling reliable electrical insulation under , and superior abrasion resistance, with rewind tests showing over 500 cycles without failure. These properties stem from the polymer's amorphous structure and strong intermolecular forces, providing thermal stability up to 180°C continuous operation (Class H rating) and resistance to chemicals like solvents, fuels, and acids. In production, PAI enamels serve as primary insulation for and transformers, offering Class H performance at 180°C with excellent mechanical toughness and chemical barrier properties that surpass epoxies in high-temperature environments. For surface applications, PAI forms protective non-stick and low-friction coatings on metals, such as in cookware or industrial components, where it provides resistance and even after boiling in saltwater. Formulations frequently incorporate blends with polyimides to enhance flexibility and overcoat compatibility, particularly in dual-coat systems over bases for improved and handling. Compared to coatings, PAI offers a higher continuous-use (up to 225–260°C short-term) and broader chemical resistance, making it ideal for demanding electrical and uses without compromising or durability.

Injection Molding

Injection molding is a primary melt-processing method for polyamide-imide (PAI) resins, enabling the production of complex, high-precision parts with thicknesses typically limited to 0.8–13 mm. The process requires specialized equipment and precise control due to the material's high melt and sensitivity to thermal degradation. Modern reciprocating injection molding machines with controls are recommended, featuring a low (1:1 to 1.5:1) and an L/D ratio of 18:1 to 24:1 to handle the shear-sensitive melt. Venting is essential to remove volatiles, and cold runner systems or hot sprue bushings are preferred over hot runners to minimize . Key process parameters include a melt of 360–382°C (nozzle at approximately 371°C), with barrel zones progressing from 304°C at the feed to 343°C at the front. Mold temperatures range from 163–232°C to ensure uniform cooling and minimize warpage. Injection pressures start at 41–55 MPa for filling, followed by 21–34 MPa hold pressure, while is maintained at 7–14 bar and screw speeds at 50–100 rpm for optimal flow. High injection speeds are used to leverage the material's shear-thinning , which reduces under high shear rates and aids filling of intricate molds. Cycle times for small parts typically range from 30–60 seconds, controlled by screw velocity and position rather than pressure and time to achieve consistent fill. PAI's hygroscopic nature necessitates thorough drying prior to molding, typically at 149°C for 8 hours in a dryer with a of ≤–40°C, achieving moisture content below 500 ppm (0.05%) to prevent and defects like splay or voids. The high melt , comparable to that of ABS or and on the order of 10^4–10^5 Pa·s at shear rates, poses challenges in flow and fill, often requiring large gates and runners; however, facilitates . Degradation risks from prolonged residence times or excessive shear heating must be mitigated through short cycles, proper purging above 371°C, and avoiding overpacking, which can lead to or discoloration. Post-processing involves annealing or post-curing to relieve internal stresses and fully develop properties, with cycles escalating from 149°C to 260°C over several days depending on part thickness (e.g., up to 17 days for parts ≤7.6 mm thick). This step enhances dimensional stability and performance. Shrinkage varies by grade, typically 0.06–0.85%, with unfilled resins like Torlon 4203L exhibiting higher rates (0.6–0.85%) suitable for prototypes, while filled grades such as 30% (5030) or carbon fiber (7130) show lower shrinkage (0.0–0.15%) for production runs requiring tighter tolerances. Draft angles of 0.5–1° are recommended for mold release.

Machining and Composites

Polyamide-imide (PAI) machining typically involves CNC turning and milling operations conducted at moderate to high cutting speeds to leverage the material's thermal stability while minimizing heat buildup and tool wear. For turning, recommended speeds range from 90 to 240 m/min using positive geometry carbide or polycrystalline diamond (PCD) tools with rake angles of 7° to 15° and feeds of 0.1 to 0.6 mm/rev; milling employs speeds of 150 to 240 m/min with similar tooling and feeds of 0.15 to 0.9 mm/rev. Coolant is optional for these processes due to PAI's high heat resistance, though flood coolant is advised for drilling and threading to evacuate chips and prevent cracking. The material's toughness results in minimal burr formation, facilitating clean finishes, while its lower elongation compared to other plastics requires careful fixturing to avoid distortion. Achievable tolerances in PAI machining are precise, often reaching ±0.05 mm for standard components and down to ±0.025 mm for high-precision parts, supported by the material's dimensional stability post-. PCD tools are preferred for long runs or tight tolerances to counter PAI's abrasiveness, ensuring surface quality without excessive tool rubbing that could induce . Post-, parts may undergo recuring to enhance and chemical resistance, though this is not always required for structural integrity. PAI composites are formed by incorporating reinforcements such as 30 wt% or to boost mechanical performance, primarily through or processes that build on injection-molded precursors. fiber-reinforced PAI, like Torlon 5030, achieves a of approximately 10-12 GPa, providing enhanced stiffness while retaining good impact resistance. Carbon fiber variants use tapes or powder impregnation methods, followed by curing at around 250°C under pressures of 7-10 MPa to consolidate the matrix and ensure fiber-matrix adhesion. These reinforcements increase modulus up to 15 GPa in carbon-filled systems without significantly compromising PAI's inherent , enabling applications in high-load environments like bushings. However, fiber orientation during processing can lead to anisotropic properties, reducing compared to unreinforced PAI, and the added complexity raises material costs substantially over base resins.

Applications

Aerospace and Automotive

Polyamide-imide (PAI), particularly under the trade name Torlon®, is widely utilized in applications due to its exceptional thermal stability, wear resistance, and lightweight properties, which enable it to serve as a metal replacement in high-stress environments. In jet engines and aircraft structures, PAI components such as thrust washers, seals, bushings, and bearing cages operate effectively at temperatures up to 260°C (500°F) while maintaining low wear rates and dimensional stability. For instance, Torlon 4203 PAI is employed in thermal isolators for the , providing electrical and thermal isolation between composite panels and bulkheads without conducting heat or risking arcing, thereby contributing to weight reduction and enhanced . Additionally, grades like Torlon 4301 and 4203 have met spacecraft materials requirements for non-metallic components, supporting their use in demanding space applications where reliability under extreme conditions is critical. These aerospace uses leverage PAI's mechanical properties, including high and low coefficient of friction, to achieve performance metrics such as over 1 million pressure-velocity (PV) units in lubricated tribological tests, far surpassing many traditional metals. PAI parts offer approximately 50% weight savings compared to equivalents, reducing overall mass and improving without compromising on or impact resistance. In one notable example, Torlon PAI clip nuts serve as non-corrosive, lightweight fasteners in assemblies, eliminating the need for additional riveting processes and further aiding in noise and vibration reduction in engine shrouds for the 737. In the automotive sector, PAI excels in and transmission components exposed to high temperatures, oils, and cyclic loading, where its chemical resistance and creep resistance ensure long-term durability. Components like axial thrust bearings, hydraulic seal rings, and rings made from Torlon grades, such as , withstand operating temperatures up to 260°C and resist degradation from lubricants and fuels, making them suitable for assemblies and systems. For example, Torlon PAI rings provide superior resistance in high-speed environments, meeting military specifications like Mil-P 46179A for demanding applications. Automotive formulations incorporating (PTFE) fillers, such as in lubricated grades, further reduce and enable non-seizing against metal counterparts, supporting over 1.5 million PV cycles in lubricated conditions. These properties allow PAI to replace heavier metal parts in automotive engines, achieving significant weight reductions—up to 50% versus —while enduring thermal cycling and aggressive fluids without loss of integrity. In transmission systems, PAI check balls and seal rings enhance responsiveness and prevent leakage at elevated pressures and temperatures around 150°C, contributing to quieter operation and improved efficiency in modern vehicles.

Electrical and Electronics

Polyamide-imide (PAI) materials are widely utilized in electrical and electronics applications due to their exceptional , high thermal stability, and resistance to , making them suitable for demanding insulation roles in high-temperature environments. These properties enable PAI to serve as a reliable insulator in components exposed to elevated voltages and temperatures, such as those in and devices. In wire enamels, PAI formulations provide Class insulation, supporting applications in transformers and electric motors with a thermal index of 220°C, allowing continuous operation at elevated temperatures without significant degradation. This enamel is often applied as a single coat or overcoat on or aluminum wires, enhancing abrasion resistance and for inverter-fed motors. For instance, PAI enamels are employed in (EV) motors to withstand the thermal stresses from high-speed operation and power conversion. As substrates in printed circuit boards (PCBs), PAI films offer robust support for high-temperature soldering processes, maintaining integrity during lead-free up to 260°C. Their dielectric constant typically ranges from 3.5 to 4.0 at 1 MHz, providing stable signal transmission in flexible and rigid-flex PCBs used in compact . PAI substrates are particularly valued in , where thin films enable bendable circuits for wearables and displays without compromising electrical performance. For connectors, PAI serves as housing material with superior resistance to arcing, attributed to its high volume resistivity exceeding 10^15 Ω·cm, which minimizes current leakage and supports reliable performance in high-voltage interfaces. This property, combined with low , makes PAI ideal for electrical connectors in aerospace-derived and automotive systems. Key advantages of PAI in these applications include a low dissipation factor of 0.001 to 0.003 at 1 MHz, ensuring minimal energy loss in high-frequency circuits, and excellent hydrolytic stability that preserves dielectric properties in humid conditions. These traits outperform many conventional insulators, reducing signal attenuation and enhancing reliability in moisture-exposed environments. Emerging developments involve PAI nanocomposites, such as those incorporating multi-walled carbon nanotubes or nanosheets, which improve shielding for antennas while maintaining low . These enable lighter, more efficient antenna substrates for next-generation communications.

Industrial and Other Uses

Polyamide-imide (PAI) finds extensive use in industrial settings for components exposed to abrasion, high pressures, and corrosive environments, particularly in pump impellers and compressor vanes where its superior wear resistance and dimensional stability outperform traditional metals. These properties enable PAI parts to operate without in harsh conditions, reducing needs in chemical and handling equipment. In the oil and gas sector, PAI is employed for seals, piston rings, and sliding vanes, leveraging its excellent , creep resistance, and chemical inertness to withstand aggressive hydrocarbons and high temperatures. For instance, high-modulus grades like Torlon 4435 provide enhanced rigidity for dynamic sealing applications in downhole tools and compressors. Medical applications benefit from PAI's biocompatible formulations and sterilizability, with grades enduring autoclaving at 135°C for reusable surgical instruments such as clamps and , where high wear resistance minimizes degradation over repeated cycles. Its radiolucency and modulus support imaging-compatible tools, while non-reactive nature ensures tissue compatibility in short-term implants or device components. PAI-based membranes exhibit high selectivity in gas separation processes, particularly for CO2/CH4 mixtures in purification, achieving permeabilities around 57 Barrers for CO2 with selectivities up to 20 at elevated temperatures. These asymmetric structures resist plasticization under high pressures, making them suitable for industrial upgrading and carbon capture. Emerging uses include PAI in wafer handling fixtures and test sockets, where low and thermal stability prevent contamination during high-vacuum processing. In the 2020s, PAI has been incorporated into separators as hierarchical porous structures, enhancing thermal stability and ionic conductivity for safer, high-energy-density cells. For prototyping, research into PAI filaments shows potential for of durable parts with extreme heat resistance, suitable for functional testing in demanding environments like mockups, though processing requires specialized high-temperature extruders. Niche markets, including devices and specialty composites, account for approximately 10-20% of PAI consumption, with growth driven by sustainable formulations in advanced composites that reduce reliance on metals. This segment is expanding at over 7% CAGR through 2030, fueled by demands for eco-friendly, high-performance materials in filtration and .

References

  1. https://digital.library.unt.edu/ark:/67531/metadc2873/m2/1/high_res_d/thesis.pdf
  2. https://www.syensqo.com/en/brands/torlon-pai
  3. https://www.ptonline.com/articles/tracing-the-history-of-polymeric-materials-part-26-high-performance-thermoplastics
  4. https://www.fire.tc.faa.gov/pdf/TC-TN-1832.pdf
  5. https://www.sciencedirect.com/science/article/pii/B9781437734690100074
  6. https://www.solvay.com/sites/g/files/srpend616/files/2018-08/Torlon-PAI-Design-Guide_EN-v5.0_0.pdf
  7. https://www.sciencedirect.com/topics/chemistry/polyamide
  8. https://www.sciencedirect.com/science/article/abs/pii/S0014305716308485
  9. https://drakeplastics.com/2019/11/01/what-is-a-polyamide-imide/
  10. https://www.researchgate.net/publication/223300545_Novel_polyamide-imidecellulose_acetate_dual-layer_hollow_fiber_membranes_for_nanofiltration
  11. https://www.prnewswire.com/news-releases/polyamide-imide-market-to-reach-usd-6689-million-by-2024-300329074.html
  12. https://nrc-publications.canada.ca/eng/view/accepted/?id=06c75579-15bb-4fb1-b403-590399c28976
  13. https://journals.sagepub.com/doi/10.1177/0967391119858555
  14. https://www.sciencedirect.com/science/article/abs/pii/S0032386120300628
  15. https://madisongroup.com/high-temperature-thermoplastics-for-extreme-conditions/
  16. https://www.researchgate.net/figure/FT-IR-Spectrum-of-Polyamide-imides-PAI-2_fig6_326635059
  17. https://pubs.acs.org/doi/10.1021/acs.macromol.1c01389
  18. http://ineosopen.org/f/io2226a.pdf
  19. https://www.sciencedirect.com/science/article/abs/pii/S0032386101002051
  20. https://www.sciencedirect.com/science/article/abs/pii/S0032386103011728
  21. https://patents.google.com/patent/US5955568A/en
  22. https://vtechworks.lib.vt.edu/bitstream/handle/10919/27771/polyimide1.pdf
  23. https://ntrs.nasa.gov/api/citations/19900016815/downloads/19900016815.pdf?attachment=true
  24. https://www.researchgate.net/publication/222650468_Structural_determination_of_Torlon_R_4000T_polyamide-imide_by_NMR_spectroscopy
  25. https://www.matec-conferences.org/articles/matecconf/pdf/2017/44/matecconf_cmpse2017_07007.pdf
  26. https://doi.org/10.1016/j.porgcoat.2015.01.013
  27. https://www.zeusinc.com/wp-content/uploads/2019/07/RESINATE-No7-Focus-On-Polyimides.pdf
  28. https://doi.org/10.1016/j.eurpolymj.2005.05.037
  29. https://www.matweb.com/search/DataSheet.aspx?MatGUID=1ca9588da84640d199959da7c00a6083
  30. https://www.makeitfrom.com/material-properties/Polyamide-Imide-PAI
  31. https://drakeplastics.com/ultra-high-performance-plastic-materials-solutions-for-your-most-demanding-applications/polyamide-imide-pai/
  32. https://www.mcam.com/en/products/shapes/extreme/duratron-pai
  33. https://www.fictiv.com/articles/torlon-pai-high-performance-plastic
  34. https://pmc.ncbi.nlm.nih.gov/articles/PMC6203221/
  35. https://www.curbellplastics.com/materials/plastics/torlon-pai/
  36. https://aipprecision.com/pressure-tested-facts-selecting-the-strongest-polymer-for-industrial-use/
  37. https://www.makeitfrom.com/compare/Polyamide-Imide-PAI/Thermoset-Polyimide-PI
  38. https://drakeplastics.com/wp-content/uploads/2020/01/Torlon-PAI-Design-Guide_EN-227547.pdf
  39. https://www.ulprospector.com/plastics/en/datasheet/1689/torlon-7130
  40. https://www.glemco.com/capabilities/material-expertise/torlon-7130-pai/
  41. https://www.wshampshire.com/wp-content/uploads/torlon.pdf
  42. https://cncplastics.com/wp-content/uploads/Torlon-4301-Data-Sheet.pdf
  43. https://www.mcam.com/en/products/shapes/extreme/duratron-pai/duratron-t4301-pai
  44. https://www.angst-pfister.com/dam/jcr:078fc988-6638-4862-ab65-1a2c2ae9e56c/APSOplast-Technical-Plastics-Engineering-Fundamentals_ENG4.pdf
  45. https://www.celanese.com/-/media/Engineered-Materials/Files/Product-Technical-Guides/chemical-resistance-general-guidance--rev-210125.pdf
  46. https://patents.justia.com/patent/20230287180
  47. https://www.elantas.com/tongling/products/wire-enamels/polyamideimide-enamels.html
  48. https://www.syensqo.com/en/brands/torlon-ai
  49. https://www.lesker.com/polymer-coatings/pdf/torlon-ai-10-for-coatings_en.pdf
  50. https://www.sciencedirect.com/topics/chemical-engineering/polyamideimides
  51. https://www.axalta.com/electricalinsulation_global/en_US/wire-enamels/what-are-wire-enamels.html
  52. http://www.chinainsulatingmaterial.com/polyester-imide-polyamide-imide/
  53. https://www.solvay.com/sites/g/files/srpend616/files/2018-08/Torlon-PAI-Processing-Guide_EN-v3.0_0.pdf
  54. https://www.solvay.com/sites/g/files/srpend616/files/2018-08/Torlon-PAI-Quick-Molding-Guide_EN-v2.5_0.pdf
  55. https://drakeplastics.com/wp-content/uploads/2024/06/Machining-Guidelines-Torlon-en.pdf
  56. https://drakeplastics.com/wp-content/uploads/2020/01/Torlon_Machining_Guidelines.pdf
  57. https://www.easiahome.com/pai-torlon-cnc-machining/
  58. https://www.professionalplastics.com/professionalplastics/content/Torlon5030datasheetPAI.pdf
  59. https://www.sciencedirect.com/science/article/pii/S2238785423008529
  60. https://trace.tennessee.edu/cgi/viewcontent.cgi?article=7397&context=utk_graddiss
  61. https://www.syensqo.com/en/brands/torlon-pai/applications
  62. https://drakeplastics.com/aerospace/aerospace-applications-torlon/
  63. https://www.professionalplastics.com/professionalplastics/content/downloads/Solvay_Torlon_Design_Guide.pdf
  64. https://aipprecision.com/torlon-pai-tough-as-metal-but-at-half-the-weight/
  65. https://drakeplastics.com/torlon-4275-comprehensive-overview/
  66. https://www.solvay.com/sites/g/files/srpend616/files/2018-10/High-Performance-Polymers-for-Automotive_EN-v2.0_0.pdf
  67. https://www.vicentetorns.com/wp-content/uploads/2021/06/06-05-2021_TDS_VTORNS_ALU_FLAT_Thermex_220.pdf
  68. https://www.gfpimaterial.com/sale-53832703-electrical-insulation-fccl-substrate-polyamide-imide-sheet-products-50-m.html
  69. https://www.substech.com/dokuwiki/doku.php?id=thermoplastic_polyamide-imide_pai_electrical_grade
  70. https://www.goodfellow.com/uk/electrical-grade-polyamide-imide-film-group
  71. https://www.usplastic.com/catalog/files/charts/TorlonElongation.pdf
  72. https://www.professionalplastics.com/professionalplastics/ElectricalPropertiesofPlastics.pdf
  73. https://www.researchgate.net/publication/379276044_Efficient_electromagnetic_interference_shielding_performance_of_polyamide_imideMWCNT-based_nanocomposites
  74. https://www.sciencedirect.com/science/article/abs/pii/S0266353821002633
  75. https://hy-proto.com/definitive-guide-to-sourcing-torlon-polyamide-imide
  76. https://www.professionalplastics.com/professionalplastics/Quadrant_ChemicalProcessingMaterialsGuide.pdf
  77. https://drakeplastics.com/oil-gas/
  78. https://advanced-emc.com/torlon-pai/
  79. https://performanceplastics.com/blog/torlon-pai-polyamideimide-for-medical-applications/
  80. https://pmc.ncbi.nlm.nih.gov/articles/PMC6804260/
  81. https://patents.google.com/patent/WO2012173776A2/en
  82. https://www.sciencedirect.com/science/article/pii/S0376738813006339
  83. https://www.researchgate.net/publication/395054824_Thermally_stable_polyamide-imide_PAI_hierarchical_porous_separator_for_lithium_metal_batteries
  84. https://www.sciencedirect.com/science/article/abs/pii/S1359836824002555
  85. https://www.reportsanddata.com/report-detail/polyamide-imide-resin-market
  86. https://www.grandviewresearch.com/industry-analysis/polyamide-imide-pai-market
Add your contribution
Related Hubs
User Avatar
No comments yet.