| HS Code | 805735 |
| Density | 0.93 g/cm³ |
| Bulk Density | 0.45 g/cm³ |
| Molecular Weight | 3.5 × 10^6 g/mol |
| Average Particle Size | 150 µm |
| Melting Point | 135 °C |
| Crystallinity | 45–50% |
| Tensile Modulus | 700 MPa |
| Tensile Stress At Yield | 17 MPa |
| Elongation At Break | >300% |
| Shore D Hardness | 60 |
| Charpy Notched Impact Strength | No break |
| Coefficient Of Friction | 0.15 |
| Water Absorption | <0.01% |
| Thermal Conductivity | 0.41 W/m·K |
| Volume Resistivity | >10^14 Ω·cm |
As an accredited Celanese UHMW-PE 5113 factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Celanese UHMW-PE 5113 is supplied in 25 kg multiwall paper bags, palletized, or 500 kg bulk bags. |
| Container Loading (20′ FCL) | Standard 20′ FCL loading: Celanese UHMW-PE 5113 in palletized bags, dry ambient container, weight evenly distributed, secured, no special ventilation. |
| Shipping | Celanese UHMW-PE 5113 is normally shipped as a non-hazardous, non-regulated polymer. Standard packaging is 25 kg moisture-resistant bags or fiber drums, palletized and shrink-wrapped. No UN number, hazard class, or DOT/IMDG/IATA labels are required. Keep dry, away from ignition sources, and follow local transport regulations. Protect from moisture and punctures. |
| Storage | Store Celanese UHMW-PE 5113 in a cool, dry, well-ventilated area. Keep containers or bags tightly closed and protect from direct sunlight, heat, moisture, and contamination. Keep away from strong oxidizers and ignition sources. Avoid dust generation and follow good housekeeping. No special temperature control is generally required; maintain ambient conditions and use first-in, first-out stock rotation. |
| Shelf Life | Celanese UHMW-PE 5113 typically has indefinite shelf life if stored cool, dry, in original packaging away from sunlight, moisture, contaminants. |
In lithium-ion battery separator production, Celanese UHMW-PE 5113 is compounded through a wet-stretch cast-film line in which the powder is dispersed into a high-boiling paraffinic plasticizer rather than being melt-extruded in a conventional screw plastication unit. The slurry formulation is typically composed of 12–18 wt% UHMW-PE 5113, 70–85 wt% paraffin oil, 5–10 wt% fumed silica, and 0.1–0.3 wt% hindered phenolic antioxidant; for separator lines requiring improved shutdown performance, an alumina or boehmite filler may replace a portion of the silica at 2–5 wt%, increasing melt strength at the expense of higher slurry viscosity. The downstream process includes slurry mixing under vacuum at 120–160 °C, feeding to a co-rotating twin-screw extruder with an L/D ratio between 40:1 and 48:1, cast sheet extrusion through a T-die at 160–190 °C, gel sheet cooling, simultaneous biaxial orientation in a tenter frame at draw ratios of 4×4 to 7×7, continuous extraction of the plasticizer with a volatile solvent, and heat setting at 95–130 °C. The finished separator is supplied as a 5–25 μm microporous membrane with pore dimensions in the 0.03–0.1 μm range and Gurley air permeability controlled between 200 s/100 mL and 600 s/100 mL. Industry compliance is governed by GB/T 36363-2018 for polyolefin separators for lithium-ion batteries, IEC 62660-3:2016 for secondary lithium-ion cells used in electric road vehicles, ASTM D882-18 for tensile properties, and ASTM D6767-21 for pore size distribution by capillary flow porometry. Terminal product types include separator rolls for lithium nickel cobalt manganese oxide and lithium iron phosphate power cells, energy storage system prismatic cells, and thin-format consumer lithium-ion pouch cells. The operational boundary is that residual plasticizer extraction below 0.3 wt% is required before cell assembly because plasticizer residue above this level increases electrolyte wetting time and can create local resistance hotspots; published data for line-specific oil removal efficiency in simultaneous tenter frames is limited and must be validated on production apparatus.
| Parameter | Range | Standard/Method |
|---|---|---|
| UHMW-PE 5113 in oil slurry | 12–18 wt% | Internal gravimetric batch control |
| Paraffinic plasticizer | 70–85 wt% | Internal process specification |
| Fumed silica | 5–10 wt% | ISO 3262-20 |
| Hindered phenolic antioxidant | 0.1–0.3 wt% | Internal batch masterbatch control |
| Separator thickness | 5–25 μm | ASTM D5947-18 |
| Pore size | 0.03–0.1 μm | ASTM D6767-21 |
| Gurley air permeability | 200–600 s/100 mL | JIS P8117 |
| Machine-direction tensile strength | 140–200 MPa | ASTM D882-18 |
The gel-spinning conversion of UHMW-PE 5113 requires dissolution of the powder in decalin or a high-boiling paraffin blend at a concentration of 5–12 wt% with 0.1–0.5 wt% hindered phenolic antioxidant based on polymer mass. Dissolution is carried out under nitrogen in a jacketed mixer at 140–170 °C until a homogeneous solution is formed; the solution is then metered by gear pump through a multi-hole spinneret with capillary diameters between 0.5 mm and 1.5 mm and quenched in a water bath at 10–25 °C. The gel filament is drawn in a first oven at 120–140 °C to a draw ratio of 20:1–40:1, followed by second-stage hot drawing at 145–155 °C, resulting in total draw ratios up to 80:1. Published production data indicate that total draw ratio determines ultimate tenacity, and attempts to exceed 80:1 without reducing residual decalin below 0.1 wt% lead to filament breakage and irregular denier. The primary industry standards relevant to downstream products include ISO 13997:2022 for cut resistance, EN 388:2016+A1:2018 for mechanical risks, NIJ Standard-0101.06 for ballistic resistance, and ASTM F2248-19 for impact resistance of protective armor; fibre tensile tenacity is measured by ASTM D885-10(2021) or ISO 20344:2021 depending on end product. Terminal product types manufactured from gel-spun UHMW-PE 5113 include cut-resistant gloves, ballistic insert panels, high-strength ropes and slings, fishing line, reinforced sailcloth, and composite laminates. The operational boundary in gel spinning is the narrow dissolution window: below 140 °C the solution does not homogenize, while above 170 °C oxidative chain scission reduces the viscosity-average molecular weight and lowers final tenacity. Batch-to-batch variation in powder bulk density between 0.42 g/cm³ and 0.48 g/cm³ alters feed accuracy in gravimetric dispensing and must be compensated by loss-in-weight calibration on the slurry hopper.
Sieved fractions of UHMW-PE 5113 between 40 μm and 300 μm are used directly in compression sintering of porous media for gas diffusion, filtration, and fluidization plates. The powder is loaded into a cylindrical or flat die, compacted at 2–15 MPa, and sintered in a forced-air or nitrogen oven at 190–210 °C for hold periods of 15–60 min depending on section thickness; the final pore structure is determined by particle size distribution, compaction pressure, and cooling rate, with median pore diameters typically from 5 μm to 80 μm. Industry compliance for these porous parts includes FDA 21 CFR 177.1520 for food-contact olefin polymers, EU Regulation 10/2011 for plastic materials intended to contact food, ISO 10993-5:2009 for medical device cytotoxicity, and ISO 4003:2021 for bubble-point pore size testing. Formulation addition ratios are generally 100 wt% UHMW-PE 5113; where electrostatic dissipation is required, conductive carbon black is added at 1–2 wt%, increasing sintered density and reducing pore openness, while retaining the powder pre-treatment at 80–100 °C for 4–8 h when relative humidity exceeds 60 %. The downstream production process includes dry blending the conductive additive in a low-shear tumble blender, filling multiple cavity molds, automated press cycles, sintering in batch ovens with temperature uniformity better than ±5 °C, and final machining of porous plates, tubes, and cones. Terminal product types include pneumatic mufflers, gas diffusion stones, breathable hydrophobic vents, aeration diffusers in wastewater treatment, filter plates for catalyst recovery, and fluidized-bed membranes. The operational limitation is that pore uniformity below ±10 μm is difficult to maintain in flat plates thicker than 40 mm because of anisotropic heat transfer during cooling; manufacturers often reduce plate thickness to maintain consistent bubble-point pressure.
In ram extrusion of UHMW-PE 5113, the powder is compacted into a heated barrel and pressed intermittently through a forming die at melt temperatures of 190–230 °C and ram pressures between 8 MPa and 30 MPa. The process is distinguished from screw extrusion by the absence of a rotating screw; feed forward is achieved by hydraulic ram displacement, and molecular weight retention is higher because shear heating is minimized. The downstream production line consists of a powder compaction station, a temperature-controlled barrel with three heating zones, a straight or profile die, and a water-cooled calibrator maintained at 10–30 °C; the ram cycle time is typically 2–10 s and line speed is limited to 0.1–2 m/h depending on cross-section. Formulation addition ratios include 100 wt% UHMW-PE 5113, with 2–3 wt% carbon black for UV stabilization and antistatic performance, 0.2–0.5 wt% hindered phenolic antioxidant, and optionally 0.5–1.0 wt% calcium stearate as a processing lubricant; published data for the specific effect of calcium stearate on ram-extruded UHMW-PE 5113 internal weld lines is limited. Relevant industry standards include ISO 11542-1:2001 for the designation of ultra-high-molecular-weight polyethylene, ASTM D4020-18 for molecular weight via dilute solution viscosity, ASTM D638-14 for tensile properties, and ISO 1183-1:2019 for density. Terminal product types produced by ram extrusion include chain guide rails, bottle conveyor wear strips, scraper blades, belt scrapers, star wheels, and guide profiles for packaging machinery. The main processing boundary is the risk of die-break or internal weld line at temperatures below 190 °C; above 230 °C, oxidative degradation can form gel particles that weaken the cross-section. Batch variation in powder particle size distribution, particularly the 150 μm coarse fraction, alters compaction density and may cause voids in thick profiles if the barrel temperature profile is not adjusted.
| Application segment | Standard/Method | Scope / Test condition |
|---|---|---|
| Lithium-ion battery separator | GB/T 36363-2018 | Polyolefin separators for lithium-ion batteries |
| Lithium-ion battery separator | IEC 62660-3:2016 | Secondary lithium-ion cells for electric road vehicle propulsion |
| Lithium-ion battery separator | ASTM D882-18 | Tensile properties of thin plastic sheeting |
| Porous sintered media | FDA 21 CFR 177.1520 | Olefin polymers for food-contact use |
| Porous sintered media | EU Regulation 10/2011 | Plastic materials intended to contact food |
| Porous sintered media | ISO 4003:2021 | Bubble-point pore size testing |
| Ram-extruded profiles | ISO 11542-1:2001 | Designation of ultra-high-molecular-weight polyethylene |
| Ram-extruded profiles | ASTM D4020-18 | Dilute solution viscosity molecular weight |
| Gel-spun fibre | ISO 13997:2022 | Cut resistance by TDM method |
| Gel-spun fibre | EN 388:2016+A1:2018 | Mechanical risks for protective gloves |
| Gel-spun fibre | NIJ Standard-0101.06 | Ballistic resistance of body armor |
| Compression molded stock | EN 1186-1:2002 | Migration testing for food contact |
Compression molding of UHMW-PE 5113 into sheet, block, and rod stock contains no external plasticizer or solvent, and the powder is filled into polished molds without precompaction when section thickness is below 20 mm. The formulation is 100 wt% UHMW-PE 5113, with optional 0.1–0.5 wt% antioxidant and 0.1–0.3 wt% zinc stearate to reduce sticking; some food-contact grades are supplied without additives. The press cycle heats the mold to 190–220 °C under 3–6 MPa initial pressure, then the pressure is raised to 10–15 MPa after densification for a hold period of 10–20 min per 10 mm of thickness, followed by cooling under pressure to below 70 °C to prevent warpage. Industry compliance includes FDA 21 CFR 177.1520 for olefin polymers in food contact, EU Regulation 10/2011 with migration testing under EN 1186-1:2002, ASTM D638-22 for tensile properties, and ISO 1183-1:2019 for density. Terminal product types include hopper and chute liners, marine fender pads, cutting boards, conveyor wear strips, and fabricated parts for bulk material handling. The processing boundary is that molded blocks above 80 mm thickness require cooling rates slower than 5 °C/min to avoid internal voids and dimensional instability; published data for industrial cooling curves of UHMW-PE 5113 in thicknesses above 100 mm is limited, and furnace thermocouple data from production runs remain the primary control input.
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Celanese UHMW-PE 5113, also designated GUR 5113 in Celanese technical documentation, is a virgin ultra-high-molecular-weight polyethylene powder supplied for ram extrusion and compression moulding of stock shapes and machined wear components. The material falls within the PE-UHMW classification described in ISO 11542-1 because its viscosity number in decalin at 135 °C exceeds 2000 mL/g and because it does not produce a measurable melt flow index under ISO 1133-1:2022. Published datasheet values for the grade include an average molecular weight of approximately 3.9 × 10⁶ g/mol by viscosity correlation to ISO 1628-3 or ASTM D4020, a density of 0.93 g/cm³ under ISO 1183-1, and a crystalline melting peak between 133 °C and 136 °C under ISO 11357-3. These values are used for incoming inspection because the resin has no conventional melt-processing fingerprint such as a stable MFR value.
The powder is not a drop-in replacement for HDPE pipe or film grades. The molecular architecture creates a sinterable compact that fuses above the crystalline melting range without forming a low-viscosity melt. This distinction is central to the product specification. The table below summarizes characteristic values reported for GUR 5113 and the standards used to determine them. The values are typical engineering references and are not lot-release guarantees; the supplier certificate of analysis remains the controlling document for a specific lot.
| Property | Test method | Typical value | Processing or design note |
|---|---|---|---|
| Density | ISO 1183-1 | 0.93 g/cm³ | Mass-to-volume conversion for hopper refill and part weight |
| Viscosity number | ISO 1628-3 / ASTM D4020 | >2000 mL/g | PE-UHMW classification; no practical MFR |
| Melting peak | ISO 11357-3 | 133–136 °C | Lower bound for sintering; upper bound limited by degradation |
| Tensile stress at yield | ISO 527-2 | 20–24 MPa | Initial design reference for machined wear strips |
| Tensile strain at break | ISO 527-2 | >300% | Ductile response under tensile overload |
| Charpy impact strength | ISO 179-1/1eA | No break | Impact loading in conveyor guide rails |
| Shore D hardness | ISO 868 | 60–70 | Machinability and surface indentation resistance |
Specimen preparation influences the reported mechanical values. Tensile bars machined from a fully fused compression-moulded sheet may show yield stress near 21 MPa under ISO 527-2, while under-sintered or porous sections can fail at lower values. For this reason, incoming-material testing on powder samples is supplemented by destructive testing on sintered plaques or extruded sections to confirm fusion quality rather than relying on resin viscosity alone.
Powder morphology is part of the specification because PE-UHMW cannot be melt-pelletized without degrading its high molecular weight. The resin is therefore delivered as a reactor powder with a controlled particle-size distribution. Bulk density under ISO 60 or ASTM D1895 is used to size hopper and mould cavities. Sieve fractions are typically reported under ASTM D1921; the acceptable band is supplier-specific. Excess fines can reduce cold-compaction density and create dust-handling issues, while coarse particles can increase fusion time and lower the density of sintered cores.
The molecular weight of 3.9 × 10⁶ g/mol implies reptation times that are many orders of magnitude longer than those of conventional high-density polyethylene. This is why sintering relies on intimate particle contact and temperatures above the crystalline melting point. Under the low-shear conditions of compression moulding, melt viscosity can exceed 10⁸ Pa·s, although capillary measurement is not well defined. The practical outcome is that the resin does not flow to fill a mould; it must be compacted into final geometry before heating.
Oxidative stability is evaluated by oxidation induction temperature or time using ISO 11357-6 or ASTM D3895. The natural grade’s stabilizer package is designed for processing rather than long-term high-temperature oxidative service. Prolonged exposure at 120 °C in air degrades the polymer; actual lifetime is affected by thickness, antioxidant concentration, and fluid media. Oxidation induction tests are run on sintered sheet rather than powder to capture the thermal history introduced by moulding.
The processing window is defined by two competing boundaries: the crystalline melting point of the powder and the onset of thermo-oxidative degradation. Ram extrusion and compression moulding equipment must hold the stock above 133 °C long enough for inter-particle diffusion, but heating above 250 °C for prolonged periods causes chain scission, discoloration, and surface oxidation. Published data for this specific configuration is limited, but industrial practice for PE-UHMW positions the heated section between 200 °C and 230 °C. The exact setpoint is adjusted by profile cross-section and ram cycle time. A heating deviation of more than ±5 °C across the die face can create central porosity or uneven skin formation in thick sections because the outer layer may fuse before the core reaches the sintering temperature.
Moisture is not a primary plasticization issue as in polyamides, but surface moisture trapped in the powder can produce voids and steam marks. When storage humidity exceeds 60 % RH, pre-drying at 80 °C for 2 hours in an air-circulating drier is a common preventive measure. The powder should not be dried at temperatures approaching the melting range because particle agglomeration can occur.
Conveying air and hopper feeder settings must be controlled to avoid fines segregation. Volumetric and gravimetric feeders used for powder feeding can display apparent density drift when powder particle-size distribution is not consistent; this is a known batch-to-batch variance factor on production lines. Sieve analysis under ASTM D1921 or equivalent particle-size methods may be specified between supplier and processor to control the fines fraction.
Because GUR 5113 has no measurable steady-shear melt flow under standard capillary rheometry conditions, process behaviour is evaluated through sintering and compaction parameters rather than MFR. The powder is charged into a mould or ram extruder, compacted cold, and then passed through a heated die or heated press cycle. The compaction phase is typically conducted at 5–10 MPa to remove void volume; the sintering phase uses 10–20 MPa on compression presses and a die wall temperature of 200–230 °C in ram extruders. The molten surface of each particle must undergo reptation across the grain boundary; molecular weight and viscosity number are direct predictors of the time required for this fusion.
The rate-limiting step is not pellet melting but inter-particle chain diffusion. Thick sections require a heat-soak time that increases with wall thickness. Operators commonly ramp the cooling under pressure at 5–15 K/min until the part is below 70 °C to reduce shrinkage voids and warpage. If cooling is too rapid, residual internal stresses can be released during machining, causing dimensional drift in finished components.
On a production-scale ram extruder with a barrel diameter between 60 mm and 200 mm, the reciprocating ram compacts powder into the heated die block in discrete strokes. A 90 mm ram can require a pressing force in excess of 60 kN at compaction pressures near 10 MPa depending on the die section. The die land length is selected to provide residence time at the sintering temperature; profiles with wall thickness above 25 mm may require multiple heating zones or lower haul-off speeds. A common failure mode is stroke-boundary lamination when the die temperature is too low or the stroke frequency is too high, resulting in incomplete fusion at the interface between successive powder charges. The condition is detected by sectioning the extruded profile and observing faint horizontal laminar lines near the centre. Adjustments to die temperature and stroke dwell time are required rather than increases in ram pressure alone.
Compression moulding of thick sheets follows a similar logic. Platen temperatures are held at 200–220 °C, and pressure is maintained during cooling. The part geometry and mould mass determine cycle time; published data for this specific configuration is limited, and each mould requires thermal mapping to verify that the core has exceeded 133 °C for an adequate time. Thermocouple placement at the core of a tool during commissioning is standard practice. Defects include centre-plane porosity, shrinkage voids at thickness changes, and vacuum voids from entrapped air. Vacuum-assisted moulds may be used to remove air before full compaction. Press pressure is held during cooling to maintain contact between the mould surface and the polymer; if pressure is released too early, the part can delaminate internally even though the outer surface appears fused.
Machining of GUR 5113 stock shapes requires sharp tools with high clearance angles because the material is ductile and can deflect away from the cutting edge. Conventional milling, sawing, and planing are used. Stress-relieving anneal after rough machining is sometimes performed at 70–80 °C for 2–4 hours to reduce dimensional change during final finishing. Actual cycles depend on part size and residual stress from the extruded or moulded stock.
Within the Celanese GUR UHMW-PE portfolio, grade differences are expressed primarily in molecular weight, particle-size distribution, and additive packages. GUR 5113 is positioned as a sinterable powder for ram extrusion and thick-section compression moulding where uniform fusion and machinability are required. Higher-molecular-weight grades such as GUR 4120 and GUR 4150, when compared under the same sintering conditions, tend to require longer heat history and may exhibit higher resistance to abrasive wear in some slurry tests, but they can be more difficult to compact in high-output ram extrusion lines. The exact comparative ranking in a specific test depends on molecular weight distribution, specimen preparation, and test geometry; published data for the specific comparative set is limited, and end-use qualification is required.
Compared with conventional HDPE, the difference is not merely incremental. HDPE grades intended for pipe or sheet extrusion exhibit measurable melt flow under ISO 1133-1:2022, typically in the range of 0.1–1.2 g/10 min at 190 °C and 2.16 kg depending on the grade. GUR 5113 does not flow under these conditions. The practical consequence is that injection moulding and conventional single-screw plastication are outside the normal processing envelope for GUR 5113. Components are produced as extruded profiles or compression-moulded sheets and then machined into finished parts.
Different product grades may include processing stabilizers, calcium stearate as an acid scavenger, or other surface treatments. The presence of these additives changes the oxidation induction time and the friction response during solid-state ram extrusion. Processors should not substitute GUR 5113 with another PE-UHMW grade solely on the basis of molecular weight because particle size distribution and additive package also influence the sintering cycle and lot-to-lot fusion.
Friction and wear data are generated with pin-on-disc or block-on-ring configurations. The dynamic coefficient of friction for PE-UHMW on polished steel under dry conditions is commonly reported in the range 0.10–0.20 using ASTM D1894; the value rises with surface roughness, temperature, and contamination. Abrasion resistance is often tested by sand-slurry circulation in accordance with ISO 15527 or by rotating drum methods; the results are comparative rather than absolute. Published data for the specific abrasive ranking of GUR 5113 against filled grades are limited; qualification on the actual conveyor or chute geometry is required.
End-use applications for GUR 5113 include chain guides, wear strips, star wheels, guide rails, chute liners, suction box covers, and other machined components in packaging, food-processing, and material-handling machinery. In these applications, the material is selected because the sintered stock shape can be machined to close tolerances and because the surface provides low sliding resistance without external lubrication. Designers should not infer suitability from hardness or tensile data alone; wear tests such as the sand-slurry method in ISO 15527 or field trials are used to confirm performance under real particle-laden or cyclic load conditions.
Chemical resistance follows the general behaviour of semicrystalline polyethylene. The material resists many aqueous salt solutions, alkalis, and dilute acids at ambient temperature, but aromatic hydrocarbons, chlorinated solvents, and strongly oxidizing acids can cause swelling or stress cracking, particularly under load. Chemical exposure should be evaluated under ISO 175 using the actual service fluid and temperature, not inferred from a general resistance table. Continuous service under mechanical load in air is typically limited to 80 °C because of oxidative ageing and creep; intermittent excursions to 100 °C may be tolerated for short periods but are not a design basis without creep and oxidative-induction-time testing under ISO 11357-6.
The natural material has limited UV resistance; outdoor applications require a UV-stabilized variant or a carbon-black masterbatch suitably dispersed during the sintering stage. Attempts to incorporate high levels of inorganic fillers into the fine powder can reduce inter-particle fusion and create machinability problems. If wear-resistant fillers or colourants are required, the suitability of the additive package for PE-UHMW sintering must be verified on the production line, because laboratory melt-blending does not replicate the powder sintering process.
When the machined parts are intended for incidental food contact, the resin may be evaluated under FDA 21 CFR 177.1520 and EU Regulation 10/2011 by the supplier. Compliance is lot- and formulation-specific and should be confirmed from the current supplier statement rather than assumed from generic PE-UHMW literature. The natural grade does not contain intentionally added heavy-metal heat stabilizers or plasticizers; therefore RoHS 2011/65/EU restrictions for lead, cadmium, mercury, and hexavalent chromium are not typically relevant to the base resin, but supplied documentation must be checked for packaging and processing aids.
Under REACH 1907/2006, the supplier is required to communicate SVHC content above 0.1 % w/w in the article as supplied. Processors should maintain the safety data sheet and the technical data sheet revision history because changes in additive stabilisation or powder surface treatment can alter sintered colour and ageing resistance without changing the base density or molecular weight.
Batch-to-batch consistency is documented by the supplier through viscosity number, density, particle-size distribution, and residual moisture. Processors that cannot access full blend data may encounter variable fusion times and machined-part warpage. A practical incoming-inspection plan therefore combines the supplier certificate of analysis with periodic compression-moulding trials and profilometer or density checks on sintered sheet cores.