| HS Code | 472335 |
| Molecular Weight | Approx. 2.0 million g/mol |
| Density | 0.93 g/cm³ |
| Bulk Density | 0.40 g/cm³ |
| Average Particle Size | 30 µm |
| Melting Point | 130 °C |
| Crystallinity | 45-50% |
| Tensile Modulus | 700 MPa |
| Tensile Strength At Break | 40 MPa |
| Elongation At Break | 350% |
| Charpy Notched Impact Strength | No break |
| Shore D Hardness | 60 |
| Vicat Softening Temperature | 80 °C |
| Thermal Conductivity | 0.41 W/(m·K) |
| Coefficient Of Linear Thermal Expansion | 2.0 x 10^-4 /K |
| Water Absorption | <0.01% |
| Dielectric Constant | 2.3 at 1 MHz |
| Volume Resistivity | >10^14 Ω·cm |
| Flammability | UL 94 HB |
As an accredited Celanese UHMW-PE 2126 factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Celanese UHMW-PE 2126 is supplied in 25 kg (55 lb) net-weight multiwall paper bags, palletized and shrink-wrapped. |
| Container Loading (20′ FCL) | Celanese UHMW-PE 2126 loaded in a 20-foot FCL container, palletized, secured, and shipped under standard dry conditions. |
| Shipping | Celanese UHMW-PE 2126 is a non-hazardous ultra-high molecular weight polyethylene. It is typically not regulated for transport by DOT, IMDG, or IATA. Proper shipping name, UN number, hazard class, and packing group: not applicable. Ship dry in original packaging at ambient temperature, avoiding moisture, contamination, and excessive heat. |
| Storage | Store Celanese UHMW-PE 2126 in a cool, dry, well-ventilated area, away from direct sunlight, heat, flames, ignition sources, and strong oxidizing agents. Keep original containers closed to prevent moisture, dust, and contamination. Avoid excessive stacking, pressure, or prolonged UV exposure. Use first-in, first-out stock rotation and maintain clean, dry conditions. Follow the manufacturer’s SDS and local regulations. |
| Shelf Life | Celanese UHMW-PE 2126 has an approximately 24-month shelf life when stored unopened, dry, cool, and protected from direct sunlight. |
In wet-process lithium-ion battery separator production, Celanese UHMW-PE 2126 is metered into a co-rotating twin-screw extruder as dry powder, while a paraffinic process oil is injected after the powder conveying zone to avoid solid-liquid demixing. The polymer fraction is typically held between 15 wt% and 30 wt% in the oil phase; lower solids reduce gel film melt strength and increase pinning line instability at the chill roll, while higher solids shift the solution into a high-viscosity regime that overloads the melt pump suction. Melt filtration at 40–60 µm screen pack is installed upstream of the T-die; the rate of pressure rise across the screen is recorded as an incoming-resin cleanliness and foreign-particulate indicator. The solution is extruded at 180–240°C and cast through a die gap suitable for a gel film thickness in the range of 500–1200 µm onto a chilled roll maintained below 30°C to lock the gel structure before solvent extraction. After the paraffinic oil is extracted, the film is biaxially stretched; for UHMW-PE wet-process separators, the machine-direction draw ratio is generally set between 5:1 and 8:1 and the transverse-direction draw ratio between 8:1 and 12:1. Heat-setting then stabilizes the microporous structure against shrinkage. The high molecular weight of 2126 broadens the gel film processing window at low polymer solids, but it also raises extruder torque and melt pump suction pressure. Separator films are validated by thickness per ASTM D374, Gurley air permeability per ISO 5636-5, and puncture resistance per ASTM F1306. Because UHMW-PE does not generate a conventional melt flow rate under ISO 1133-1:2022 conditions, separator manufacturers qualify incoming lots by particle-size distribution per ISO 13320, bulk density per ISO 60, and residual metal content rather than by melt flow ratio. Published data for 2126-specific draw ratio and heat-setting temperature optimization is limited; each separator line must map gel strength, extraction rate, and transverse-direction necking behavior on its own tooling.
In ram extrusion of UHMW-PE chain guides, wear strips, and conveyor rail profiles, the resin is not plasticated by screw shear; it is periodically compacted into a heated die by a reciprocating ram. Output stability is governed by powder feed density, ram sealing friction, preheat temperature uniformity, and die land back-pressure. Celanese UHMW-PE 2126 is supplied as a high-bulk-density powder; incoming bulk density is monitored per ISO 60 because even small lot-to-lot shifts alter the compacted preform height and die fill. The ram preheat zone is typically operated at 150–200°C, the die body at 180–230°C, and the downstream calibration zone at a lower temperature to fix the final profile cross-section. Because the material does not form a conventional melt, the sintered strand must be cooled under controlled back-tension to prevent internal void formation and thermal stress. A recurring production failure mode is stick-slip at the ram sealing ring; the resulting pressure pulsation produces density bands that appear after machining as alternating white and translucent rings. Through-thickness tensile elongation per ISO 527-3 is used to detect these fusion defects. Oxidation is the second limiting factor; prolonged residence in the preheat zone reduces oxidation induction time when measured by ISO 11357-6. Production lines running long campaigns frequently use nitrogen sweep around the ram preheat section to reduce yellowing and die-lip residue. The finished profile may be tested for tensile yield stress and elongation per ISO 527-3, while wear resistance is evaluated by end-user-specific methods because sand-slurry, dry-sand rubber-wheel, and sliding-wear tests rank UHMW-PE differently. Compression set and creep under load are application-specific and require testing under ISO 899-1 when the profile is used in bolted or clamped rail systems.
For sanitary food-contact stock shapes, compression molding of Celanese UHMW-PE 2126 is performed by charging dry powder into a hydraulic hot press after the mold reaches 195–210°C. The applied specific pressure is usually held at 10–20 MPa, and the heating cycle must be long enough for the core to pass through the polyethylene crystalline melting range without exceeding the oxidative degradation onset. Insufficient soak produces an unfused powder core that displays low through-thickness elongation and local delamination during subsequent CNC machining. Cooling is performed under maintained clamp force until the average part temperature drops below 60°C; otherwise large sheets warp or develop residual stress gradients that cause late-stage dimensional drift. Molded density near 0.930 g/cm³ per ISO 1183-1 is used as a first-pass fusion check, but density alone is insufficient because trapped oxidative degradation can produce densified surface domains while the core remains underfused. Food-contact compliance for molded parts is evaluated under FDA 21 CFR 177.1520 for olefin polymers and EU Regulation 10/2011 for plastic food contact materials, with migration testing conducted in the intended food simulant and time-temperature condition. Surface cleanliness in production is often monitored by isopropyl alcohol swab extraction followed by gravimetric residue measurement. The practical continuous service limit is below 90°C for high-load food machinery applications because creep of UHMW-PE increases as temperature approaches the alpha-relaxation region; exact load-bearing limits require creep testing per ISO 899-1. The main processing incompatibility is oxidative degradation when mold sealing leaks admit oxygen at the 200°C+ molding temperature. Regrind incorporation must be validated by ISO 11357-6 OIT and through-thickness tensile elongation, not by melt flow ratio, because the resin does not produce a conventional melt flow value under ISO 1133-1:2022.
In gel spinning of high-tenacity UHMW-PE filament, the resin is dissolved in a high-boiling aliphatic or naphthenic solvent at a polymer concentration between 2 wt% and 10 wt%. Celanese UHMW-PE 2126 produces a high solution viscosity at those solids; spinneret pack pressure must be managed with high-pressure metering pumps and sintered metal filtration at 20–40 µm. The solution is extruded through a multi-orifice spinneret into a water or air-quench bath to form gel filaments, which are subsequently extracted and hot-drawn in multiple stages. Draw ratios above 45:1 are common for ballistic and cut-resistant fiber products; at that stage, residual extraction solvent in the gel filament becomes a major tenacity-limiting variable because solvent plasticizes the polyethylene and suppresses crystal orientation. Yarn tenacity is measured by ASTM D2256; cut resistance of the finished textile by EN 388; fabric tensile strength by ISO 13934-1. In anti-ballistic laminates, specific energy absorption is not described by a single international standard but is evaluated through backface deformation testing in internal or national ballistics programs. The high molecular weight of 2126 supports high draw-induced tenacity, but the lot-to-lot solution viscosity must be controlled by solution viscometry because no ordinary melt flow test applies. Published 2126-specific draw ratio and solvent retention data are limited; fiber producers must establish the spin-pack filtration cycle and extraction train residence time on their own line.
Sintered UHMW-PE 2126 fluidization plates, pneumatic muffler vents, and water treatment air diffusers are produced by free-sintering of compacted powder preforms rather than by melt extrusion. The powder is compacted cold or warm in a mold at a pressure between 10 MPa and 40 MPa, then heated to 180–210°C for a controlled soak. The void fraction and pore throat size are set by the starting powder particle-size distribution, the compaction pressure, and the thermal cycle; unlike melt-formed porous polymers, the sintered preform retains a semi-continuous powder-boundary structure. Pore size distribution is measured by mercury intrusion porosimetry per ASTM D4284 or by bubble point per ASTM F316 for membrane-like grades. Air permeability is commonly measured by ISO 4022 for sintered porous products; however, end users may specify pressure drop under their own face velocity. The trade-off is mechanical strength: as porosity increases to improve airflow, tensile strength and burst resistance decrease, so each application must specify a maximum differential pressure. For fluidization plates in powder conveying, the critical failure mode is not tensile yield but surface attrition and pore plugging at the plate underside; surface hardness is therefore measured by the Shore D method per ISO 868. For pneumatic silencer vents, the sintered disk is press-fit into a metal or polymer housing; interference fit must account for UHMW-PE thermal expansion, which is approximately 1.5×10⁻⁴ K⁻¹ to 2.0×10⁻⁴ K⁻¹ in the solid state. ISO 178 flexural modulus tests are used to qualify incoming resin lot consistency because slight changes in molecular weight distribution affect sintered particle fusion and flexural ductility. Published data for 2126-specific porous structure response across compaction pressure gradients are limited; the above ranges are typical industrial starting conditions for UHMW-PE sintered media.
Machined Celanese UHMW-PE 2126 components used in semiconductor wet benches, valve bodies, and wafer transport guides are produced from compression-molded stock rather than injection-molded parts to avoid molded-in stress and orientation. The machining process produces a characteristic micro-fuzz surface because UHMW-PE does not shear cleanly under conventional tooling; post-machining annealing below the crystalline melting point and then precision burnishing or diamond tool finishing are used to reduce particle release. Surface roughness is controlled by profilometer measurements under ISO 4287. Ultrapure water contact components are qualified under SEMI F57, which sets extractable limits for metallic and organic contaminants after exposure to ultrapure water; total organic carbon and resistivity decay are the standard lot-release metrics. Because 2126 is a high-molecular-weight ethylene polymer, it does not contain plasticizers, but residual catalyst metals and machining lubricants must be removed by cleanroom detergent extraction and thorough deionized water rinsing. Dimensional stability after machining is verified by conditioning to equilibrium moisture and temperature; UHMW-PE has negligible water absorption but a relatively high thermal expansion coefficient, so fluid contact at elevated temperature changes clearance fits. The material is generally compatible with dilute acids and alkalis used in semiconductor cleaning baths, but oxidative chemicals such as hot concentrated nitric acid or ozone-containing ultrapure water can reduce surface molecular weight and increase particle shedding. Chemical compatibility is validated through specific exposure protocols under SEMI F57 or ASTM D543. A typical compliance matrix for stock shapes entering semiconductor and food-contact machining cells is shown in Table 1.
| Standard or regulation | Application boundary |
|---|---|
| FDA 21 CFR 177.1520 | Olefin polymer food-contact components up to the specified end-use temperature and food type |
| EU Regulation 10/2011 | Plastic food contact materials and articles; migration testing in the intended simulant |
| SEMI F57 | Ultrapure water contact components in semiconductor process tools |
| REACH SVHC | Article duty; requires supplier communication for substances above 0.1 wt% in the article |
| RoHS 2011/65/EU | Electrical/electronic equipment scope; applies to homogeneous material concentrations of restricted metals |
| ISO 11357-6 | Oxidation induction time for incoming resin and regrind process control |
| ASTM D543 | Chemical compatibility after exposure to process fluids |
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