| HS Code | 501133 |
| Chemical Family | Ultra-high molecular weight polyethylene (UHMWPE) |
| Density | 0.93 g/cm³ |
| Molecular Weight | 2.0 million g/mol |
| Average Particle Size D50 | 50 µm |
| Melting Point | 130-135 °C |
| Crystallinity | 45-50 % |
| Tensile Modulus | 700 MPa |
| Tensile Stress At Yield | 17 MPa |
| Elongation At Break | 300 % |
| Charpy Notched Impact Strength | No break at 23 °C |
| Water Absorption | <0.01 % |
| Coefficient Of Friction | 0.2 |
| Thermal Conductivity | 0.4 W/m·K |
| Coefficient Of Linear Thermal Expansion | 150 µm/m·°C |
| Vicat Softening Temperature | 80 °C |
| Volume Resistivity | >10^14 ohm·cm |
| Dielectric Constant 1 Mhz | 2.3 |
| Fda Compliance | 21 CFR 177.1520 |
As an accredited Celanese GUR UHMWPE 4012 F factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Celanese GUR UHMWPE 4012 F is supplied in 25 kg polyethylene-lined paper bags, palletized for industrial shipment. |
| Container Loading (20′ FCL) | Celanese GUR UHMWPE 4012 F is packed bagged on pallets and loaded into a 20-foot FCL container under dry conditions. |
| Shipping | Celanese GUR UHMWPE 4012 F is shipped as a non-hazardous, free-flowing ultra-high molecular weight polyethylene powder in moisture-resistant bags or boxes. It should be kept dry, clean, and protected from contamination and prolonged direct sunlight; it is not classified as dangerous goods for transport. |
| Storage | Store Celanese GUR UHMWPE 4012 F in a cool, dry, well-ventilated area away from direct sunlight, heat, sparks, flames, and strong oxidizing agents. Keep containers tightly closed in original packaging to prevent moisture and contamination. Avoid dust generation, protect from UV, and maintain good housekeeping. |
| Shelf Life | Celanese GUR UHMWPE 4012 F has an indefinite shelf life when stored dry, sealed, and protected from light and contaminants. |
Celanese GUR UHMWPE 4012 F is a virgin ultra-high-molecular-weight polyethylene powder supplied in the fine particle size range used for gel processing, ram extrusion, compression moulding, and dry sintering. The viscosity number measured in accordance with ISO 1628-3:2010 places the grade above the melt flow threshold; capillary melt flow rate testing according to ISO 1133-1:2022 does not yield a measurable MFR, and density of the natural polymer is 0.930–0.940 g/cm³ under ISO 1183-1:2019. Industrial data sheets for the grade report a bulk density near 0.40 g/cm³ and residual moisture below 0.01 wt% after drying, which reduces hydrolytic degradation during oven sintering and gel spinning. The downstream scenarios below are limited to applications where 4012 F is actually run on production-scale equipment: battery separator film, high-tenacity gel-spun yarn, porous sintered media, ram-extruded wear stock, compression-moulded food-contact stock shapes, and electrostatic powder coating for impact-abrasion linings.
Wet-process lithium-ion battery separator film converts 4012 F into microporous membranes through thermally induced phase separation. The powder is metered through a loss-in-weight feeder into a co-rotating twin-screw extruder with an L/D ratio of 40:1–56:1, where paraffin oil is injected downstream of the melting zone. Polymer loading is controlled at 18–35 wt% for single-layer UHMWPE separators; the balance is paraffin oil, with 0.1–0.5 phr hindered phenolic antioxidant and, in silica-modified grades, 0.5–3.0 phr fumed silica. The melt solution is discharged through a slot die at 160–220°C, cast onto a chilled roller to form an oil-filled gel film, and passed through sequential extraction baths. Methylene chloride or n-hexane removes the paraffin oil; residual oil must be reduced below 0.1 wt% before the dried film enters the transverse stretching unit, because residual oil causes blocking on the TD tenter clips and non-uniform pore formation. The stretched film is then heat-set at 110–130°C to lock the microporous structure. Compliance for separator qualification uses IEC 62660-3:2022 and UL 1642 for cell-level safety; separator tensile properties are measured with ASTM D882, and ionic resistance is evaluated by electrochemical impedance spectroscopy. Terminal product types include single-layer UHMWPE separators for lithium-ion cells in electric vehicle packs and stationary energy storage systems.
Process control on a separator line is concentrated at the gel film casting and extraction interface. Cast roll temperature must be held between 20°C and 60°C to prevent oil sweat-out on the film surface; if the cast film is quenched too rapidly, the surface pores close while the core retains oil, producing a gradient that raises the Gurley number. After extraction, the film passes through a multi-roll dryer where residual solvent is measured online by near-infrared analysers; the target residual is below 0.1 wt% for oil and below 50 ppm for methylene chloride before heat-setting. The transverse stretching unit, typically a tenter chain with 8–12 zones, sets the final pore aspect ratio. Publications covering UHMWPE wet-process separator manufacture note that processing conditions are strongly coupled to the paraffin oil viscosity grade; lower-viscosity oil improves dispersion but lowers gel strength, while higher-viscosity oil preserves film integrity at the expense of extraction speed.
In gel spinning, the powder is converted into a solution in which the polymer concentration is deliberately kept below the quiescent chain overlap concentration to reduce entanglement density before drawing. In decalin, the concentration is controlled between 5 wt% and 10 wt%; in mineral oil, the band is 8–15 wt%. Concentrations below these bands produce filament breaks under spinneret drawdown, while higher concentrations prevent the solid-state draw ratios above 50:1 that are needed for tensile modulus above 100 GPa. The solution is prepared in a co-rotating twin-screw extruder with an L/D ratio near 40:1, heated to 150–180°C, filtered through a 10–20 µm sintered metal pack, and extruded through spinneret capillaries of 0.5–1.0 mm diameter into a water or solvent quench bath. Gel filaments are extracted with n-hexane or heptane; residual solvent above 0.05 wt% before hot drawing creates microvoids and lowers tensile strength. Multi-stage drawing at 130–150°C increases total draw ratio to 50:1–80:1. Compliance for cut-resistant gloves is tested under EN 388:2016+A1:2018 and ISO 13997; ballistic laminates are tested under NIJ 0101.06; yarn tensile properties are evaluated using ASTM D885. Terminal product types include cut-resistant sleeves, fishing lines, maritime ropes, and unidirectional laminate precursors for ballistic plates and helmets.
The gel spinning process has an upper temperature limit set by chain scission rather than viscosity. At dissolution temperatures above 180°C in air, oxidative degradation reduces the viscosity-average molecular weight and the final yarn tenacity; in decalin, the spin solution is therefore blanketed with nitrogen and the extruder vent is maintained under slight negative pressure. Spin pack pressure is a key process indicator; a rise from 50 bar to 80 bar over a run indicates gel build-up in the filtration media and can create surface defects on the filament. In the drawing section, the first-stage draw ratio is deliberately limited to 4:1–6:1 because excessive early orientation raises the glass transition of the gel fibre and reduces the maximum total draw ratio. These operational constraints are documented in industrial fibre spinning of ultra-drawn UHMWPE fibres.
For porous sheets, tubes, and fluidization plates, dry-powder sintering of 4012 F relies exclusively on interparticle fusion without full densification. The powder is classified to a controlled particle size cut; for aeration and filtration media, D50 is selected between 100 µm and 200 µm depending on target pore size. No binder or chemical blowing agent is added; the powder is filled into a mould, compacted cold at 2–8 MPa, and sintered in a forced-air convection oven at 190–220°C. Soak time is scaled at 10–30 min/mm of wall thickness. Pore size after sintering is governed by particle size distribution, compaction pressure, and heating rate rather than by additive loading. The main process defect is temperature overshoot in the core of thick plates, which collapses the surface pores while leaving the centre weakly fused; stepped heating profiles with an intermediate dwell at 150°C reduce this gradient. Compliance for food-contact porous components references FDA 21 CFR 177.1520 and EU 10/2011; filtration performance is assessed by bubble point and air permeability methods adapted from porous-media testing, although published data for this specific grade in porous filtration configuration is limited. Terminal product types include silo fluidization cones, filter plates, aeration pads for wastewater basins, and vacuum table porous plates.
Porosity in sintered 4012 F is not uniform unless the mould is heated with an external gas flow and the part is individually cooled. Large parts such as silo cones with 30–50 mm wall thickness require two-stage heating because the thermal diffusivity of UHMWPE powder is low; the outer surface reaches sintering temperature long before the core. If the oven setpoint is simply raised to 220°C at the start, the surface can melt and collapse the pores while the core remains at 120–140°C. The accepted industrial method is to dwell at 150°C for 30–60 min before ramping to 200°C, then cool under nitrogen at 2–5°C/min. The final bubble point pressure is then correlated with the D50 of the powder cut and the cold compaction pressure.
In ram extrusion lines for 4012 F, a hydraulically driven plunger compacts the powder charge through a heated die tunnel because the material cannot be conveyed by a rotating screw under standard conditions. The powder is fed into a receiver, pressed forward, and fused in the die at 180–230°C; the cooling section then reduces the profile below its crystallisation temperature under back pressure. Unfilled ram-extruded stock is standard, but when the terminal part operates in explosive or electrostatic-sensitive environments, 0.5–2 wt% carbon black or graphite masterbatch is added; for dry sliding friction reduction, 0.5–3 wt% MoS₂ or silicone masterbatch is compounded in a dry mixer before ram feeding. Filler addition above 3 wt% disrupts the compaction front and produces transverse welds that fail under cyclic loading. Compliance for raw material specification is established by ASTM D4020-18 and ISO 11542-1:2001; machined test specimens are evaluated for tensile properties using ASTM D638-14 and for hardness using ASTM D2240. Terminal product types include chain guides, wear strips for bottling conveyors, bed rails, and scraper blades in mineral slurry handling.
Die design for 4012 F ram extrusion differs from that used for PTFE or HDPE because the absence of a melt pool means heat transfer into the powder bed is the rate-limiting step. The die is divided into a heated fusion zone, a transition zone, and a cooling zone; die land length is typically 8–15 times the profile diameter. If the transition zone is too short, the outer skin fuses before the core and the extrudate exhibits a radial weld line. Production lines therefore use upper and lower die heaters with individual temperature controllers and thermocouples spaced at 50–80 mm intervals. Post-extrusion annealing is performed in heated air or water at 90–120°C for 1–2 h to relieve residual stresses before machining.
Compression moulding of 4012 F into dense sheet and rod stock avoids screw-induced molecular weight degradation and yields machined blanks for food-processing machine components. The mould is filled with virgin powder and compressed at 5–15 MPa while the platen temperature is raised to 190–230°C; holding time is scaled at 15–25 min/cm of maximum wall thickness. After the hold, the mould is cooled under pressure at 5–15°C/min to reduce internal voids and dimensional warpage. The formulation is 100% virgin UHMWPE; no plasticisers, stabilisers, or external lubricants are added, which avoids migration of low-molecular-weight species under hot water, steam, or acidic food contact. Compliance is governed by FDA 21 CFR 177.1520 for olefin polymers, with additional migration testing under EU 10/2011 and overall material suitability under EC 1935/2004. Terminal product types include star wheels, scraper blades, conveyor guide shoes, and chain wear plates for food and beverage lines.
Because food-contact stock shapes are often machined by end users, the blank must be supplied with a uniform crystalline structure and flatness tolerance. Rapid cooling from 200°C to room temperature can generate a quench-hardened surface layer that warps after machining; controlled cooling at 5–15°C/min under pressure is therefore specified. In plants that mould thick blocks of 100 mm or more, the core temperature must be monitored by inserted thermocouples because the centre cools slower than the surface and can remain above 100°C for several hours. Demoulding before the core drops below 80°C leads to post-mould shrinkage and loss of flatness.
On preheated steel substrates, powder coating with 4012 F deposits the polymer directly on steel or stainless steel surfaces without melt compounding. Corona-charged spray guns apply the fine powder to metal surfaces preheated to 150–180°C; the coated substrate is then oven-sintered at 200–240°C. Single-pass films above 1.5 mm tend to sag before gelation, so linings up to 4–6 mm are built by successive spray-sinter cycles. The coating charge is normally 100% 4012 F; if fluidisation or electrostatic transfer is unstable in humid plants, 0.1–0.5 wt% fumed alumina or silica is added as a dry flow aid. Compliance for industrial equipment linings falls under RoHS Directive 2011/65/EU and REACH Regulation (EC) No 1907/2006; potable-water contact requires additional testing under NSF/ANSI 61. Published data for this specific grade in electrostatic powder coating is less abundant than for ram extrusion and separator films, but fine particle size and high melt viscosity support the process. Terminal product types include hopper liners, mixer blades, chute liners, and dishwasher basket coatings.
Adhesion to the substrate is mechanical rather than chemical because UHMWPE does not polarise or accept primers readily. The steel surface is grit-blasted to a profile of 50–100 µm before heating; without surface profile, the sintered coating delaminates under impact. In hot-humid plants, the powder is conditioned to 20–25°C before spraying because moisture pickup raises the powder resistivity and collapses the electrostatic cloud. The oven sintering time is set by the mass of the metal part, not by coating thickness; heavy sections may require 20–40 min at temperature while thin sheet metal may sinter in 5–10 min.
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