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| HS Code | 720064 |
| Material | Polyoxymethylene (POM) |
| Chemicalformula | (CH2O)n |
| Density | 1.41-1.42 g/cm³ |
| Meltingpoint | 165-175 °C |
| Glasstransitiontemperature | -60 °C |
| Crystallinity | 75-85% |
| Tensilestrength | 60-80 MPa |
| Youngsmodulus | 2.6-3.5 GPa |
| Elongationatbreak | 15-45% |
| Waterabsorption | 0.2% at 24 hours |
| Thermalconductivity | 0.30 W/(m·K) |
| Volumeelectricalresistivity | 1×10^14 to 1×10^15 Ω·cm |
| Chemicalresistance | Resistant to solvents, fuels, and weak alkalis; attacked by strong acids and oxidizing agents |
| Uvresistance | Poor unless stabilized |
As an accredited Polyoxymethylene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Polyoxymethylene supplied as virgin pellets in 25 kg moisture-resistant bags, sealed to prevent degradation during transport and storage. |
| Container Loading (20′ FCL) | Polyoxymethylene resin packed in 25 kg bags on pallets, loaded into a 20′ FCL container, secured and moisture-protected. |
| Shipping | Polyoxymethylene (POM) ships as non-hazardous solid pellets or powder. Keep dry and away from excessive heat, sparks, or open flames, as fine dust may be combustible. Use clean, sealed containers or bags, protect from mechanical damage, and follow standard handling procedures for polymers to prevent contamination and moisture uptake. |
| Storage | Store Polyoxymethylene (POM) in a cool, dry, well-ventilated area away from direct sunlight, heat, and ignition sources. Keep containers tightly sealed to prevent moisture absorption and contamination. Avoid contact with strong acids, oxidizers, and peroxides. Maintain moderate temperatures to minimize formaldehyde emission and material degradation. Use original packaging or compatible inert containers. |
| Shelf Life | Store in a sealed container in a cool, dry area away from heat and sunlight; shelf life is typically 12 months. |
Fuel sender flanges, ORVR valves, and quick-connect couplings molded from acetal copolymer are processed in hot-runner tools with valve-gate diameters of 0.6 mm to 1.0 mm and asymmetric gate sequencing to displace weld lines away from O-ring seal grooves and barbed retention features. The material is selected against a baseline of polyamide 6/6 because acetal copolymer shows lower equilibrium moisture uptake of 0.8% per ISO 62 and no significant plasticization in alcohol-containing fuel blends; this prevents a shift in the sealing interface radius after 30 d immersion in fuels. In thin-walled flanges with nominal wall thickness of 2.0 mm, the melt flow rate of 9 g/10 min at 190 °C under 2.16 kg load per ISO 1133-1:2022 allows flow-path length-to-thickness ratios up to 150:1 without short shot, provided hold pressure is maintained between 60 MPa and 80 MPa for the entire gate freeze time. High injection velocity above 200 mm/s produces shear heating within the acetal backbone, but melt temperature at the nozzle must not exceed 230 °C; at 235 °C or above, atmospheric formaldehyde releases appear at the mold parting line and can be detected by Draeger tube sampling, with readings above 1 ppm triggering a shutdown condition in high-volume plants.
Barrel temperature profiles for screw diameters of 40 mm to 60 mm in production extruders are set with rear zone 180 °C, center zones 200 °C to 215 °C, and nozzle 215 °C; the screw L/D ratio is 20:1 to 25:1 with compression ratio of 2.5:1, which is sufficient because acetal is a crystalline melt with a sharp phase transition. The tool surface temperature is controlled at 90 °C to 100 °C to achieve through-thickness crystallinity and minimize post-mold warpage of the sealing plane. Depending on part mass, cooling time is set to 12 s to 18 s; ejection at wall temperatures above 120 °C leads to distortion of snap-fit retention arms. Post-molding dimensional checks on a coordinate measuring machine are performed after 48 h at 23 °C and 50% RH per ISO 291 to allow post-shrinkage of 0.1% to 0.2% following demolding. Hot-plate welding of the flange to a polyethylene fuel tank shell uses a plate temperature of 230 °C and weld time of 15 s; insufficient plate temperature below 210 °C leaves a cold weld line that fails axial tensile testing. Ultrasonic welding of acetal to acetal at 20 kHz and amplitude 40 µm requires a near-field joint design with a shear interference of 0.25 mm to 0.35 mm because acetal’s low molecular friction generates less interfacial heat than amorphous polymers.
Fuel-contact validation in OEM fuel sender programs typically uses the surrogate fluids of SAE J1681, specifically Fuel C, CE 10, and CM 15, with continuous immersion at 60 °C for 500 h to 1,000 h. The acceptance metrics are tensile strength retention after drying per ISO 527-2:2012 and dimensional change measured on coupons per ISO 175. Acetal copolymer grades containing a 2-hydroxypropyl-terminated stabilizer package exhibit lower mass loss in Fuel C at 60 °C than homopolymer, but published comparative data for long-term alcohol exposure beyond 1,000 h is limited. Permeation through the flange is assessed gravimetrically with an aluminum cup fixture at 40 °C, but this test does not substitute for full tank SHED testing under customer specification. In production, the presence of ethanol in fuel blends above 15% does not soften the acetal surface but increases stress-cracking risk at sharp internal corners, so all interior radii are held above 0.5 mm and the gate area is annealed at 130 °C for 30 min to eliminate frozen-in molded-in stress.
In printer paper-feed gear trains and automotive HVAC actuator gearboxes, unfilled POM homopolymer is specified for its short-term flexural modulus of 2,800 MPa per ISO 178, but the actual design limit is creep modulus under intermittent load at the operating temperature of the gearbox housing. The drive gears in a paper path are subjected to tooth bending stresses of 20 MPa to 35 MPa at 1,000 Hz engagement; under these conditions, acetal copolymer with a creep modulus of 1,100 MPa at 1,000 h and 60 °C per ISO 899-1 will exhibit flank deformation that increases transmission error over 106 cycles. The design remedy is to derate the tooth root bending stress to 15 MPa for unfilled POM and to use a wider face width to lower the specific load. POM homopolymer provides a higher short-term tensile strength of 70 MPa but is less stable in moist air due to acid-catalyzed depolymerization; the copolymerized comonomer units interrupt the oxymethylene sequence and reduce the unzipping rate as shown by lower formaldehyde formation in melt maintenance tests.
Tooling for acetal gears is typically a 4-cavity or 8-cavity cold-runner mold with a three-plate pin-point gate to balance fill to each tooth. The cavity layout must compensate for anisotropic mold shrinkage of 1.8% along the flow direction and 1.5% transverse to flow at a nominal wall of 2.0 mm; CAD tooth profile is pre-distorted through iterative injection simulation and verified by coordinate measurement against ISO 1328-1 accuracy class 8. The mold is run with a coolant inlet temperature of 80 °C to 90 °C, not the lower settings used for amorphous materials, because acetal’s crystallinity at the gear tooth surface increases resistance to wear. When reground acetal is used at 15 wt% to 20 wt% with virgin pellets, the melt flow rate shifts upward by 2 g/10 min to 3 g/10 min, and the pack pressure must be reduced to avoid overpacking the gate area and creating a hard spot at the tooth root. Surface inspection under 10x magnification looks for microcracks at the gate vestige and splay at the tooth flank; splay originates from trapped volatiles and is eliminated by pre-drying at 80 °C for 2 h when the material has been stored at relative humidity above 60%.
For low-noise gear trains, compounded grades of POM with 20 wt% PTFE micropowder reduce the coefficient of friction against acetal or polyamide from 0.35 to 0.20 but lower tensile modulus to approximately 1,900 MPa. Wear volume in block-on-ring testing per ISO 7148-2 is reduced by approximately 40% compared with unfilled acetal, but the PTFE phase migrates to the part surface during injection and can alter printability and adhesive bonding of the gear hub. Silicone oil additives at 2 wt% provide a similar friction reduction without the same tensile loss, yet the oil exudes to the tooth flank during heated storage and can contaminate adjacent paper-path rollers. Gear tooth failure in service is dominated by pitting at the pitch line and root cracking caused by high-frequency cyclic loading; notched Charpy impact strength of unfilled POM at 6 kJ/m² per ISO 179-1/1eA is adequate at room temperature but drops to 3 kJ/m² at -20 °C, so ambient-temperature gear layouts that survive drop tests may fail in cold-cycle validation of the printer.
| Formulation | Tensile modulus (ISO 527-2) | Notched Charpy (ISO 179-1/1eA) | Coefficient of friction against steel, dry |
|---|---|---|---|
| Unfilled acetal copolymer | 2,600 MPa | 6 kJ/m² | 0.35 |
| 20 wt% PTFE-modified | 1,900 MPa | 4 kJ/m² | 0.18 |
| 2 wt% silicone-modified | 2,300 MPa | 5.5 kJ/m² | 0.22 |
| 25 wt% glass-fibre-reinforced | 7,000 MPa | 3 kJ/m² | 0.40 |
POM homopolymer is used in multi-dose insulin pen dose dials and dry-powder inhaler dose counters because the unfilled grade produces smooth internal ribs with no glass-fibre filler and low abrasion against the metal return spring. The structural plastic is selected only after verifying that the final device does not require steam sterilization; acetal is not recommended for autoclave cycles above 121 °C because saturated steam hydrolyzes the acetal backbone and releases formaldehyde. Gamma irradiation also imposes a narrow window: an absorbed dose of 25 kGy per ISO 11137-1 causes chain scission and a measurable reduction in notched Charpy impact, while residual formaldehyde may exceed supplier limits unless the components are degassed for 14 d at 40 °C after exposure. Electron-beam sterilization at doses below 25 kGy is often preferred for small acetal parts because the exposure time is shorter and oxidative degradation is reduced compared with cobalt-60 gamma sources, but color shift from white to pale yellow is still observed in unstabilized homopolymer.
Injection molding of medical acetal components is carried out in a white-room classification of ISO 14644-1 Class 8 or higher with tooling dedicated to the grade to prevent cross-contamination. The melt temperature is held at 200 °C to 215 °C for homopolymer; higher temperatures increase the concentration of formaldehyde released at the nozzle and can exceed the 0.5 mg/m³ workplace exposure limit during a 15 min short-term sampling period when ventilation is inadequate. Mold deposit formation is controlled by reducing the barrel residence time to 5 min to 8 min and by using a low-compression screw with a ratio of 2.1:1 to lower shear input. The running parameters are documented in the device master validation file because a shift of injection speed from 50 mm/s to 90 mm/s alters crystallinity at the snap-fit arm and can change the insertion force of the dial mechanism by 8% to 12%. Post-molding annealing at 130 °C for 1 h stabilizes the internal dimensions but may embrittle the thin snap features; therefore, the cycle is validated by assembling the pen and testing the dose increment pull-out force per the OEM specification.
Biocompatibility is established on the final component rather than the resin alone, but medical POM suppliers typically provide data packages with ISO 10993-5, ISO 10993-10, ISO 10993-11, and USP <88> Class VI. Non-migration of processing aids into drug formulations is evaluated by extraction with a polar and non-polar solvent under the stated contact time; if the pen dose dial is not in direct liquid contact with the drug solution, the justification is based on indirect contact risk under ISO 10993-1:2018. The table below summarizes the acceptance scheme for a drug-delivery component in which POM is the only patient-contacting material during use.
| Evaluation | Reference standard | Acceptance basis |
|---|---|---|
| Cytotoxicity | ISO 10993-5 | No more than grade 2 cell lysis or reactivity |
| Intracutaneous irritation | ISO 10993-10 | No erythema or oedema score greater than 1 |
| Acute systemic toxicity | ISO 10993-11 | No mortality or significant body weight loss |
| USP biological reactivity | USP <88> Class VI | No irritation or systemic reaction from extract injection |
| Food-contact resin compliance | 21 CFR 177.2470 | Migration within regulatory end-use limits |
Municipal water-meter piston chambers and irrigation pump impellers are injection-molded from acetal copolymer with nominal wall thickness of 2.0 mm to 3.0 mm; the material is chosen over polyamide because its moisture uptake at saturation is below 1.0% per ISO 62, limiting the swelling-induced clearance change in the metering chamber to less than 0.15% at 23 °C in distilled water. The operational boundary for chlorinated water is a free chlorine concentration of 0.5 mg/L at 23 °C; above 1.0 mg/L or at sustained water temperatures above 60 °C, oxidative attack of the acetal backbone produces microcracks at the piston sealing edges and a measurable increase in particulate release. Published long-term data for continuous exposure to chloramine in recirculating loops is limited, and the component must be validated in the actual water chemistry rather than relying on producer datasheets.
Impeller designs for small centrifugal pumps use acetal copolymer at rotational speeds up to 3,000 rpm without glass reinforcement because the short-term tensile strength of 60 MPa to 65 MPa is sufficient for hub stress at the shaft bore. Glass-fibre-reinforced acetal with 25 wt% chopped glass raises flexural modulus to about 7,000 MPa but reduces elongation at break from 30% to 3%; this excludes thin snap-fit hub retention and makes the impeller sensitive to assembly cracking. The pump manufacturer compensates for acetal’s lower thermal conductivity by limiting the dry-run period to 10 s at 0.5 m/s peripheral speed; beyond this, the friction at the shaft bore heats the hub above 100 °C and causes localized melting or seizure on stainless steel rotors. A hexagonal bore is preferred over a circular bore with a flat because the geometry distributes torque without sharp keyway corners; the bore is molded with draft angle of 0.5° to 1.0° on each side and post-machined only if the pump specification requires bore roundness within 0.02 mm.
Water-contact compliance for acetal used in meter internals is evaluated under AS/NZS 4020 in Australian approval programs or under the relevant national drinking-water test scheme; the pass criterion includes no visible microbial growth and low extractable organic carbon. In production, pre-drying at 80 °C for 2 h is mandatory when the resin has been stored at relative humidity above 60% because surface moisture is drawn into the melt and produces splay on polished piston sealing surfaces. Processors operating hydraulic injection machines with clamp force above 1,500 kN report that gate-freeze time is the main bottleneck in multi-cavity impeller tools; the gate is a direct edge gate of 1.5 mm diameter to allow the holding pressure to propagate through the hub, but this gate creates a visible witness mark that must be trimmed flush to maintain hydraulic balance.
In low-voltage relay bases and terminal blocks rated for pollution degree 2 under IEC 60664-1, unfilled acetal copolymer provides a comparative tracking index above 600 V, corresponding to PLC 0 under IEC 60112. The minimum creepage distance for a working voltage of 250 V is then set by the printed circuit board layout rather than by the terminal block plastic; this allows smaller pitch between adjacent terminals than would be possible with polyamide 66, which also meets 600 V but swells more in humid storage. In sealed relay applications, acetal is selected with a formaldehyde-scavenging additive because equilibrium formaldehyde release from the molded base at 80 °C can deposit as an insulating film on silver-nickel contacts. The scavenger addition increases MFR from 9 g/10 min to 13 g/10 min, so barrel zone temperatures are reduced by 5 °C to 10 °C compared with standard material to avoid flashing thin partition walls of 0.6 mm.
Unfilled acetal is rated UL 94 HB at 0.8 mm; flame-retarded acetal compounds that achieve V-2 or V-0 are used only where the end-product standard imposes a glow-wire ignition requirement of 850 °C under IEC 60695-2-11, because the unfilled resin does not claim a pass at 1.0 mm thickness. The same component may pass a 750 °C glow-wire contact test but fails if material loss or flaming persists beyond 30 s; this is a practical lower wall-thickness boundary for terminal blocks subject to unattended-appliance standards. The production molding window is tightened to melt temperature 200 °C to 215 °C and screw back pressure 5 bar to 10 bar; high back pressure above 20 bar increases shear heating and produces volatile formaldehyde at the nozzle, while low back pressure below 5 bar gives non-uniform melt color and weak weld lines at the metal-insert retainers. Insert molding of brass screw terminals is performed with insert temperature above 100 °C to prevent a cold interface that cracks during thread torque testing at 0.5 N·m to 1.0 N·m.
POM homopolymer is injection-molded into aerosol valve stems with a critical outer diameter of 3.00 mm ± 0.02 mm and an integral metering chamber that must remain flash-free at the annular sealing edge. The tolerance stack-up is controlled by molding the stem in a 32-cavity tool with a coaxial core pin of 1.50 mm and a gate at the base of the stem; the gate witness is recessed below the sealing land and is inspected to a maximum protrusion of 0.03 mm. Sampling at critical dimensions is performed under ISO 2859-1 general inspection level II with an AQL of 0.65 for the sealing land and 1.0 for the dip tube retention barb. Process capability on the outer diameter is monitored by a laser gauge with a repeatability of 0.001 mm; mold temperature is held at 90 °C to 100 °C and the cavity pressure at gate freeze is controlled at 55 MPa to 65 MPa to reduce shot-to-shot variation from 0.015 mm to 0.008 mm.
The acetal grade used in aerosol valve internals is a low-extractable homopolymer that resists dimensional change in aliphatic hydrocarbon propellants and common fragrance solvents; however, the material is not used for valve components in contact with water-based formulations containing chlorine or strong oxidizing agents because surface microcracking can appear after long shelf storage. Weight loss tests are carried out by exposing molded stems to propellant A-46 at 40 °C for 28 d; the acceptable weight change is less than 0.1% and the stem must show no visible blistering or softening. In formulation work, low-viscosity grades with an MFR of 27 g/10 min are used for thin-wall stems, but the higher MFR lowers notched Charpy from 6 kJ/m² to 4 kJ/m² and makes the barb more prone to stress-whitening during dip-tube assembly, so the tube interference is reduced from 0.10 mm to 0.06 mm relative to standard material. Multi-component valve assemblies that include POM stems must be checked for migration of low-molecular-weight oligomers into the product concentrate; extractables are quantified by gas chromatography after reflux in 95% ethanol for 6 h, with the acceptance limit set by the customer formulation specification rather than by a universal standard.
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Polyoxymethylene (POM) is a semi-crystalline engineering thermoplastic built from repeating -CH2-O- units. Commercial designations under ISO 1043-1 distinguish POM-H homopolymer from POM-C copolymer. The homopolymer is produced by anionic polymerization of formaldehyde and contains terminal hydroxyl groups that can initiate thermal depolymerization, while the copolymer incorporates oxyethylene comonomer at 1.0–3.0 mol% to interrupt chain-end unzipping. Under ISO 1183-1, unfilled POM-C density is typically 1.41 g/cm³ and POM-H density is 1.42 g/cm³. Differential scanning calorimetry per ISO 11357-3 gives POM-C melting peaks of 162–173 °C and POM-H peaks of 175–183 °C. These structural parameters govern specification choices for machined wear components, injection-moulded gears, conveyor links, and automotive fuel-system hardware.
The repeating oxymethylene unit produces crystallinity of 70–80% for POM-C and 75–85% for POM-H. This high crystallinity yields a coefficient of linear thermal expansion of 1.0–1.2 × 10−4 K−1 by ISO 11359-2 and a heat deflection temperature at 0.45 MPa of 150–160 °C for POM-C and 160–170 °C for POM-H by ISO 75-2/B. The polymer retains mechanical response to moderate sub-zero service because the alpha relaxation onset is near −60 °C. This combination separates POM from general-purpose HDPE or PP, which have lower stiffness and lower continuous-use temperature limits.
In thick-section machined bar stock, POM-H typically exhibits Rockwell M hardness of 88–94 versus 78–84 for POM-C. Tensile stress at yield for POM-H is commonly 68–75 MPa under ISO 527-2, while POM-C falls between 60–67 MPa. Flexural modulus of POM-H can reach 3,200–3,500 MPa, whereas POM-C is nearer 2,700–3,000 MPa by ISO 178. The higher crystallinity of POM-H contributes to hardness and stiffness but also increases centerline porosity risk in rod diameters above 80 mm unless slow cooling is used on industrial extrusion lines. POM-C, with its comonomer content, has a broader thermal processing window and better resistance to hot-water and alkaline hydrolysis. For bearing shells and gear blanks, machining cell trials show POM-H gives lower wear in dry running steel shafts but is less tolerant of humid coolant; POM-C is selected when chemical exposure and dimensional stability in wet environments dominate. Batch-to-batch variation in POM-H bar stock is controlled by ultrasonic inspection for centerline porosity and by density measurement per ISO 1183-1; batches with void indications are diverted to small-diameter machining blanks.
| Property | POM-C | POM-H | Test method |
|---|---|---|---|
| Density | 1.41 g/cm³ | 1.42 g/cm³ | ISO 1183-1 |
| Tensile stress at yield | 60–67 MPa | 68–75 MPa | ISO 527-2 |
| Flexural modulus | 2,700–3,000 MPa | 3,200–3,500 MPa | ISO 178 |
| Rockwell M hardness | 78–84 | 88–94 | ISO 2039-2 |
| Melt volume-flow rate | 4–27 cm³/10 min at 190 °C/2.16 kg | 2–14 cm³/10 min at 190 °C/2.16 kg | ISO 1133-1 |
| Melting peak | 162–173 °C | 175–183 °C | ISO 11357-3 |
Injection moulding of POM is carried out on reciprocating-screw machines with melt temperatures of 180–215 °C for POM-C and 190–220 °C for POM-H, with the lower set points used for thin-wall geometries. Mold temperature is maintained at 60–100 °C for POM-C and 80–120 °C for POM-H to obtain adequate crystallinity for dimensional tolerance control. Screw L/D ratios of 20:1 to 25:1 and low-shear non-return valves are used, and a clamp force of 0.5–0.8 tonnes per cm² of projected area is common. Surface moisture above 0.10% by weight requires pre-drying at 80 °C for 3–4 h; excess water produces surface splay and hydrolytic molecular weight loss. Above 230 °C, POM depolymerizes with formaldehyde evolution. Barrel residence time at maximum melt temperature is therefore limited to 10 min in 35 mm screw machines, and production operators monitor vent gas odor and surface pitting on purged parts.
| Parameter | POM-C | POM-H |
|---|---|---|
| Melt temperature | 180–215 °C | 190–220 °C |
| Mold temperature | 60–100 °C | 80–120 °C |
| Drying | 80 °C for 3–4 h | 80 °C for 3–4 h |
| Melt volume-flow rate per ISO 1133-1 | 4–27 cm³/10 min at 190 °C/2.16 kg | 2–14 cm³/10 min at 190 °C/2.16 kg |
In unlubricated pin-on-disc testing under ASTM G99 at 0.5 m/s and 0.5 MPa, POM-C typically shows lower volume loss than unfilled PA66 because PA66 absorbs 2.5–3.0% moisture at 50% RH, softening the surface and widening the wear scar. PBT shows lower moisture absorption than both but has a lower limiting pressure-velocity value in continuous dry running according to industrial bearing test programs. Creep behavior of POM-C at 23 °C under 10 MPa is characterized by slow logarithmic strain; published data for this specific configuration is limited, but long-term gear tooth deflection is lower than PA66 at 60 °C and 60% RH because POM-C does not plasticize as strongly with water. Compared with UHMW-PE, POM-C offers higher creep resistance and machinability, while UHMW-PE has superior impact toughness at cryogenic temperatures and a lower coefficient of friction against stainless steel. POM-C is selected over UHMW-PE where tight part tolerances and higher modulus are required.
POM bearing grades are often modified with PTFE at 5–20 wt% to reduce slip-stick and dynamic coefficient of friction to 0.08–0.15. Lubricated grades containing silicone oil or aramid fiber are used in automotive window regulators and office machine gears, where noise generated by PA66 parts at 40 °C and 80% RH is reduced by the acetal surface. These compounds are produced on co-rotating twin-screw extruders with L/D 40:1 using downstream feeding for glass or PTFE to limit shear heating. The specific wear rate measured by ASTM G99 is load- and counterface-dependent; published data for this specific configuration is limited, but grade-specific values are available from supplier tribology reports.
Chemical resistance of POM-C is characterized by insolubility in common aliphatic and aromatic hydrocarbons, automotive fuels, glycols, and many neutral solvents at ambient temperature. It is not recommended for continuous exposure to strong mineral acids above 5% concentration, nitric acid, or hydrolyzing aqueous solutions above 80 °C. In 90 °C hot water, tensile strength retention falls below 70% after 1,000 h; the failure mode is surface erosion and molecular weight loss, although published data for this specific configuration is limited. Contact with chlorinated solvents and brake fluids should be evaluated by immersion testing per ISO 175 at 60 °C for 168 h; condensation polymer alternatives such as PBT or PPS may be required for hot aggressive media. The limiting oxygen index of unfilled POM is approximately 15%; flame-retardant grades are less common than for polyamides. Unfilled POM usually has a dielectric strength of 20 kV/mm at 1 mm thickness per IEC 60243-1 and a comparative tracking index above 600 V per IEC 60112.
In automotive fuel-sender assemblies, POM-C is used for injection-moulded float arms and resistance-card guides because it retains dimensions in gasoline and E10 fuel and does not swell excessively in humid fuel-tank headspace. PA66 parts in the same assembly would absorb 2.5% moisture at 50% RH and produce tooth-profile growth in the mating gear rack. POM-C does not suffer stress-corrosion cracking from road salt, a failure mode observed in some zinc-alloy castings. However, when POM-C replaces brass in valve guides and stem components, the pressure-temperature rating is limited by the polymer’s creep resistance, and hot-water service above 60 °C is generally excluded from plumbing certifications. Production-scale fuel-line molding cells have shown that POM-C parts must be kept below 0.10% moisture before molding to avoid splay and voids in snap-fit features. Ultrasonic inspection of moulded valve guides is used to reject internal porosity.
Commercial POM product lines include unfilled, 10%, 20%, and 30% glass-fiber reinforced grades, mineral-filled low-warp grades, PTFE-modified bearing grades, carbon-fiber antistatic grades, and UV-stabilized grades. A 25 wt% glass-fiber POM-C typically raises flexural modulus to 8,000 MPa and reduces elongation at break to 2–4%. Specifications are organized under ISO 9988-1 and ASTM D6778, with the designation block including POM-C or POM-H and the melt volume-flow rate at 190 °C/2.16 kg. Food-contact POM-C grades are available that comply with FDA 21 CFR 177.2470 and EU Regulation (EU) 10/2011 for repeat-use articles when the supplier’s migration test data are followed. Electrical and drinking-water grades may carry IEC 60112 tracking index certification and cold-water NSF/ANSI 61 listings. REACH and RoHS compliance is grade-specific; the purchaser should request the full product certificate rather than infer compliance from the polymer family alone. POM grades are not suitable for direct contact with strong oxidizing acids, hot concentrated alkaline solutions above 60 °C, or continuous hot-water service above 80 °C without validation.