| HS Code | 836383 |
| Materialtype | Ultra-high molecular weight polyethylene (UHMWPE) |
| Polymerfamily | Polyethylene |
| Molecularweight | 2.0 x 10^6 g/mol |
| Density | 0.930 g/cm³ |
| Bulkdensity | 0.45 g/cm³ |
| Particlesize | 150 µm |
| Meltingpoint | 135 °C |
| Crystallinity | 45% |
| Tensilestrengthatyield | 17 MPa |
| Tensilestrengthatbreak | 40 MPa |
| Tensilemodulus | 700 MPa |
| Elongationatbreak | 300% |
| Hardnessshored | 60 |
| Notchedizodimpact | No break |
| Waterabsorption | <0.01% |
| Thermalexpansioncoefficient | 1.5 x 10^-4 /°C |
| Thermalconductivity | 0.4 W/m·K |
| Dielectricconstant | 2.3 |
| Volumeresistivity | >10^15 ohm·cm |
| Chemicalresistance | High |
| Wearresistance | High |
| Coefficientoffriction | 0.1-0.2 |
| Maximumusetemperature | 80 °C |
| Processingmethod | Compression molding, ram extrusion, injection molding |
| Color | White |
| Form | Powder |
As an accredited Celanese GHR UHMWPE 8020 factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Celanese GHR UHMWPE 8020 is supplied in 25 kg moisture-barrier paper sacks, palletized for industrial handling and storage. |
| Container Loading (20′ FCL) | 20′ FCL container loading for Celanese GHR UHMWPE 8020: palletized bags, shrink-wrapped, uniformly stacked, and secured for safe ocean transport. |
| Shipping | Celanese GHR UHMWPE 8020 is generally shipped as a non-hazardous, non-UN-classified polymer solid under normal freight. Use sealed, clean bags or drums on pallets; protect from moisture, heat, UV, and contamination. Follow the SDS, supplier packaging instructions, and applicable local transport regulations. |
| Storage | Store Celanese GHR UHMWPE 8020 in a cool, dry, well-ventilated area away from direct sunlight, heat, ignition sources, and strong oxidizers. Keep containers closed and in original packaging to prevent moisture and contamination. Avoid dust generation and accumulation; use appropriate housekeeping and follow the SDS. |
| Shelf Life | Celanese GHR UHMWPE 8020 is stable when stored cool, dry, and protected from UV and contamination; confirm exact shelf life with the manufacturer. |
In gel-spinning lines that process Celanese GHR UHMWPE 8020 powder into high-tenacity filaments, the initial slurry is prepared by dispersing the powder at 4–6 wt% in a paraffin-oil/decalin mixture heated to 140–160°C under a nitrogen blanket; the dissolution stage is held until a homogeneous gel free of unmelted powder agglomerates is observed, because undispersed particles nucleate draw-induced defects. Dissolution is normally carried out in a co-rotating twin-screw unit with an L/D ratio of 25:1 to 40:1 and segmented screw elements that distribute shear without exceeding 160°C melt temperature. The gel is then metered through a gear pump to a spinneret with capillary diameters between 0.5 mm and 2.0 mm at a throughput of 1–5 g/min per hole, followed by a 5–25 mm air gap and quench bath at 10–25°C to fix the gel filament dimensions. After extraction of the paraffin oil with n-hexane in a counter-current washing train, the gel yarn is hot-drawn at 110–150°C using multi-stage godets to a cumulative draw ratio of 30:1 to 80:1. The resulting filament tensile properties, measured according to ASTM D885-19, typically fall in the range of 2.5–3.5 GPa tenacity and 80–120 GPa modulus, with elongation at break of 2.5–4.5%; these values support cut-resistant glove construction tested to EN 388:2016+A1:2018 and ANSI/ISEA 105:2016 using the ASTM F2992-15 TDM method, as well as unidirectional composite panel lay-ups for ballistic protection tested to NIJ Standard-0101.07. The main process conflict in this application is oxidative chain scission at the extraction and drawing stages; therefore, the extracted gel must not be held at temperatures above 80°C for more than a few minutes before drawing, and oxygen content in the drawing tunnel should remain below 5 vol% to limit gel yellowness and loss of tenacity. Batches with higher fines content require a reduction in initial slurry concentration by 0.5–1.0 wt% to avoid torque excursions on the dissolution extruder.
Biaxial orientation of solvent-extracted polyethylene membranes for lithium-ion separators is conducted on cast film produced from a blend of HDPE, the 8020 powder, and a paraffin-oil plasticiser at a plasticiser loading of 60–75 wt%. The presence of the UHMWPE fraction raises the elongational viscosity and entanglement density of the melt, which prevents web necking when the cast film enters the transverse-direction orienter at line speeds above 60 m/min. After extrusion through a T-die at 200–230°C and chill-roll casting to a thickness of 80–300 µm, the film is biaxially stretched in machine direction at a ratio of 5:1 to 9:1 and in transverse direction at 7:1 to 12:1 at 90–120°C; the paraffin oil is then extracted with methylene chloride or n-hexane, and the membrane is heat-set at 120–130°C to reduce residual stress. Residual plasticiser in the final separator is controlled below 500 ppm by gas chromatography, because higher residues depress electrolyte wettability and increase thermal shrinkage. The final separator thickness is typically 7–20 µm, with porosity of 38–50% tested to ASTM D2873 and Gurley air permeability of 200–400 s/100 mL tested to ASTM D726-94. The shutdown response of the separator is governed by the melting point of the polyethylene fraction at 130–135°C, while the UHMWPE chain network maintains separator continuity up to 150°C sufficiently to reduce the risk of electrode contact. The relevant cell-level safety verification for the terminal product is conducted under IEC 62660-3:2022 or UL 1642, and the separator itself must demonstrate puncture resistance measured according to ASTM D3763 with a needle-probe fixture at a penetration speed of 50 mm/min.
| Parameter | Standard method | Typical control window |
|---|---|---|
| Final separator thickness | ASTM D5947-18 | 7–20 µm |
| Porosity | ASTM D2873 | 38–50% |
| Gurley air permeability | ASTM D726-94 | 200–400 s/100 mL |
| Shutdown temperature | ISO 11357-3 | 130–135°C |
| Meltdown temperature | ISO 11357-3 | >150°C |
| Puncture strength | ASTM D3763 | 300–500 gf |
When bottling-line guide rails are produced by ram extrusion, the 8020 powder is pre-dried at 80°C for 3–4 h when ambient relative humidity exceeds 60%, because residual moisture generates steam porosity in the solid-state compacted profile. Ram extrusion is carried out on a reciprocating ram machine with a barrel bore between 25 mm and 150 mm, barrel temperature zones set at 180–220°C, and a die temperature of 200–230°C. During each ram cycle, the powder is compacted under a ram pressure of 15–35 MPa, and steady-state back-pressure is maintained above 18 MPa; a drop below this threshold indicates oversized porosity, die wear, or insufficient feed, and the profile will show reduced density and lower wear resistance. Typical extrusion speeds for conveyor rail profiles are 2–6 m/h for cross-sections up to 60 mm × 40 mm, and the die land length is set to 20–40 mm to control a die swell ratio observed between 1.2 and 1.8. The extrudate is spray-cooled to 60–80°C before sawing and machining into wear strips, chain guides, and bottle starwheel inserts for high-speed filling lines where line speeds exceed 40 m/min. Mechanical acceptance is based on ISO 527-2 tensile strength of 17–22 MPa, ISO 868 Shore D hardness of 60–70, and ASTM D4020 wear testing in comparison with a reference UHMWPE control. Food-contact compliance for the finished articles is evaluated according to the matrix below.
| Regulation | Scope | Test condition | Limit |
|---|---|---|---|
| FDA 21 CFR 177.1520 | Olefin polymers for food contact | Extraction per 21 CFR 176.170 | No volatile colour or odour |
| EU 10/2011 | Plastic food-contact materials | OM2 per 2 h at 70°C | 10 mg/dm² |
| GB 4806.7 | Plastic food-contact materials | 4% acetic acid, 65% ethanol | 10 mg/dm² |
| NSF/ANSI 51 | Food equipment materials | End-use exposure simulation | No migration limit exceedance |
For porous tubes sintered from the 8020 powder, the powder bed is first vibrated in a cylindrical mold at a frequency of 40–80 Hz and amplitude of 0.5–1.5 mm to achieve a packing density that determines the final pore-size distribution; sieved powder fractions in the 100–250 µm range typically yield a mean flow pore diameter of 8–25 µm after sintering, while finer fractions below 75 µm generate membranes with pore diameters below 5 µm but with higher pressure drop. Sintering is carried out in a convection oven at 180–200°C for 30–60 min for wall thicknesses up to 25 mm, with no external pressure applied; the powder particles fuse at their contact points while retaining the interconnected void network. Bubble point pressure is measured by ASTM F316 and typically falls between 0.03 MPa and 0.15 MPa for the described pore-size ranges, while air permeability is measured by ASTM D737. The resulting porous parts are inspected for permeability using air at 125 Pa, and filtration efficiency is evaluated by ISO 16889:2022 multi-pass testing when the tubes are used as hydraulic filter elements. Terminal parts include silencer elements in pneumatic systems, air diffuser tubes in wastewater aeration basins, and depth-filter cartridges for aggressive chemical service. A limitation of this fabrication route is the low collapse strength of thin-walled porous tubes; wall thickness below 6 mm can fail under radial loads above 0.3 MPa, so reinforced support cores are required for pressure-driven filtration.
In solid-state compression moulding of the 8020 powder with a peroxide crosslinking agent at 0.5–1.5 wt%, the blend is dry-mixed in a low-shear ribbon blender for 15–30 min at 25°C, then compacted in a hydraulic press at 200–220°C and 10–20 MPa for 20–40 min, followed by cooling to 60°C before demoulding. Gel fraction after crosslinking is measured by ASTM D2765 after xylene extraction at 140°C for 12 h and is typically held between 85% and 95% to balance wear resistance and residual ductility. The crosslinked product is tested for wear rate by ASTM G99 against a hardened steel counterface at 0.5 m/s and 5 MPa nominal contact stress; crosslinked UHMWPE typically shows a wear volume reduction of 30–50% relative to the non-crosslinked reference, but elongation at break measured to ISO 527-2 falls to 80–150% from the original >300%. This trade-off is acceptable in bushings and slide bearings that operate at PV limits up to 0.5 MPa·m/s, but not in impact-dominated components such as dock bumpers where high elongation is a design requirement. For applications requiring lower coefficient of friction, 5–15 wt% PTFE micro-powder is added, and 2 wt% carbon black is used where outdoor UV exposure is present. Terminal components include trunnion bushings, marine cutless bearing sleeves, and cam followers in food packaging machines; each batch is subject to ASTM D4020 molecular-weight retention testing and ISO 21304-1 material specification checks.
Because large-area compression moulding of the 8020 grade is performed on multi-daylight presses with clamp capacities of 1000–3000 t, the powder is loaded into a preheated mould at 40–60°C and then consolidated at 200–220°C under 5–15 MPa for 30–60 min depending on sheet thickness, which commonly ranges from 6 mm to 40 mm. Cooling under pressure to below 55°C is necessary to prevent warpage in sheets wider than 1.5 m; otherwise the release of frozen-in orientation creates edge curl that exceeds 2 mm/m. The moulded sheets are then cut and welded to form dump-truck bed liners, hopper liners, and silo discharge cones. Sliding abrasion resistance is evaluated with ASTM G65 using dry sand/rubber-wheel abrasion at 130 N load and 143 m sliding distance; UHMWPE liners typically show volume loss below 20 mm³ in this test, although abrasive particle angularity can double the measured wear rate. Impact resistance at low temperature is confirmed by ISO 974 brittle-temperature testing, and the material remains ductile down to −150°C, provided the moulded sheet is not contaminated with low-molecular-weight wax. For outdoor service, 2 wt% carbon black masterbatch is dry-blended with the powder before consolidation to provide UV stabilization; without this addition, surface embrittlement can occur within 12 months of full-sun exposure. Dimensional stability after annealing at 80°C for 24 h is controlled below 0.5% shrinkage, measured in accordance with ISO 11542-2.
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