| HS Code | 168261 |
| Density | 0.93 g/cm³ |
| Molecularweight | 1.2 x 10^6 g/mol |
| Bulkdensity | 0.40 g/cm³ |
| Averageparticlesize | 30 µm |
| Meltingpoint | 135 °C |
| Crystallinity | 45 % |
| Tensilemodulus | 700 MPa |
| Elongationatbreak | 350 % |
| Notchedcharpyimpactstrength | No Break |
| Abrasionresistance | 100 mm³ |
| Waterabsorption | <0.01 % |
| Thermalconductivity | 0.41 W/m·K |
| Coefficientoffriction | 0.15 |
| Vicatsofteningtemperature | 80 °C |
| Form | Powder |
As an accredited Celanese UHMW-PE 4112 F factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Celanese UHMW-PE 4112 F is supplied in 25 kg multiwall paper bags or 1000 kg bulk bags, palletized and shrink-wrapped. |
| Container Loading (20′ FCL) | 20′ FCL: 16 pallets of Celanese UHMW-PE 4112 F, 25 kg bags, 1,000 kg/pallet, total 16,000 kg net, palletized. |
| Shipping | Celanese UHMW-PE 4112 F is a non-hazardous, non-regulated solid polymer, typically shipped in moisture-resistant bags, boxes, or octabins on pallets. Transport at ambient temperature, keep dry, and avoid contamination, punctures, and direct sunlight. Follow the supplier’s SDS and local transport regulations. |
| Storage | Store Celanese UHMW-PE 4112 F in a cool, dry, well-ventilated area, away from direct sunlight, heat, sparks, and flames. Keep containers tightly closed, labeled, and off the floor. Prevent moisture ingress and excessive dust generation. Use grounding and bonding where dust may accumulate. Avoid strong oxidizing agents. Maintain good housekeeping and follow the supplier’s safety data sheet. |
| Shelf Life | Celanese UHMW-PE 4112 F has a shelf life of 24 months when stored in original packaging under dry, cool conditions. |
In high-energy-density lithium-ion cell assembly, Celanese UHMW-PE 4112 F is wet-processed into microporous shutdown separator film. The powder is pre-dried at 70 °C for 2 h when ambient relative humidity exceeds 60 %. A representative masterbatch contains 18–25 wt% polymer, 70–78 wt% liquid paraffin with a kinematic viscosity of 40–100 cSt at 40 °C, and 0–6 wt% fumed silica. Silica addition above 6 wt% increases die pressure and reduces biaxial stretchability. Premixing is carried out in a jacketed high-speed mixer held at 40–60 °C. The blend is then fed to a co-rotating twin-screw extruder with an L/D ratio of 40:1 and vacuum venting. Melt temperature at the die is maintained between 170 °C and 210 °C; screw speed is set at 350–500 rpm. A T-die delivers a cast film of 0.2–0.5 mm onto a chill roll held at 20–40 °C. The solidified film is biaxially stretched at 90–115 °C to ratios of 5.0–6.0 in machine direction and 5.0–7.0 in transverse direction. Paraffinic oil is extracted with methylene chloride or n-hexane at 25–40 °C until residual oil content falls below 200 ppm. Heat setting follows at 110–125 °C with 2–5 % relaxation. The finished film develops a Gurley value of 200–400 s/100 mL as measured by ASTM D726-23, porosity of 40–50 % by ISO 15901-1:2016, and a shutdown temperature between 130 °C and 135 °C. Cell-level thermal runaway compliance is assessed under IEC 62660-2; separator puncture strength is reported according to ASTM F1306-21. In this configuration the separator functions as a thermally activated current-interruption layer that collapses pore structure near the polymer melting point while retaining melt integrity above 150 °C. Terminal products include pouch, prismatic, and cylindrical lithium-ion cells for electric vehicles and grid storage. Published data for the dissolution and extraction kinetics of 4112 F in separator-grade films are limited; the parameters above reflect the class behaviour of UHMW-PE with similar powder morphology and particle size distribution.
Neat 4112 F powder is processed without antioxidants or processing aids in reciprocating ram extrusion. This method is preferred over single-screw plastication because the high melt viscosity of UHMW-PE prevents stable screw conveying at molecular weights above 1.0 × 10⁶ g/mol. The powder is compacted in a temperature-controlled barrel with a hydraulic plunger at 30–50 MPa. Die land temperature is set between 200 °C and 230 °C; die land length is maintained at 150–300 mm to allow complete sintering without excessive oxidation. Output is governed by a reciprocating cycle of 30–90 s. Extruded profiles are cooled in air at 2–5 °C/min to below 50 °C before band-saw cutting and CNC routing. A die entry compression ratio of 2:1 is typical for solid wear profiles. The resulting components are used as star wheels, curved guide rails, and worm scrolls on high-speed beverage filling lines. Food-contact compliance is established under FDA 21 CFR 177.1520 for olefin polymers and EU 10/2011 with an overall migration limit of 10 mg/dm². Abrasion resistance is characterised by ASTM G65-16 Procedure A; published comparative data for UHMW-PE show volume loss below 100 mm³ after 6000 revolutions under a 130 N load. For unlubricated sliding against carbon steel, the continuous PV limit is approximately 0.07 MPa·m/s; exceeding this limit produces localised frictional heating and surface melting. Service temperature under continuous load is limited to 80 °C. Terminal profile cross-sections typically range from 20 mm × 20 mm to 100 mm × 50 mm; wall thickness below 10 mm is difficult to control in ram extrusion because sintering heat transfer is too rapid to establish a stable melt front. Published data for this specific 4112 F configuration in beverage-line ram extrusion are limited; process parameters are transferred from UHMW-PE grades with equivalent bulk density and particle size.
Gel spinning converts UHMW-PE into high-tenacity fiber by dissolving the polymer below its degradation temperature and preventing chain folding during drawing. The 4112 F powder is dispersed in decalin or white mineral oil at a concentration of 5–12 wt%. Dissolution is carried out under nitrogen at 130–160 °C until a homogeneous gel is formed. The solution viscosity at the spin pack is maintained between 1,000 Pa·s and 5,000 Pa·s at 150 °C; values below 1,000 Pa·s cause jet breakage, while values above 5,000 Pa·s raise die pressure beyond 200 bar and degrade spinnability. The gel is extruded through a spinneret with capillary diameter 0.8–1.5 mm and capillary L/D ratio 2–4 at 160–180 °C. The filament is quenched in water at 10–20 °C to set the gel network. The spin draw ratio is kept between 1.0 and 3.0. After solvent extraction and drying, the fiber is hot-drawn at 120–150 °C to a total draw ratio of 30–60. The resulting fiber exhibits tenacity of 2.4–3.5 GPa and tensile modulus of 90–120 GPa when tested under ASTM D3822-14. Cut-resistant glove liners are certified under EN 388:2016, with UHMW-PE-containing yarns typically reaching cut level 5 under the ISO 13997:2022 TDM test. Ballistic panel inserts are assessed under NIJ 0101.06. Residual decalin is controlled below 100 ppm to meet REACH substance restrictions for textile articles. The main operational boundary is oxidative chain scission during dissolution; antioxidant addition at 0.05–0.10 wt% is required when residence time exceeds 30 min. Published data for the specific gel-spinning behaviour of 4112 F are limited; dissolution time and gel uniformity should be verified on a pilot spin line before specifying this grade for high-tenacity fiber campaigns.
For wastewater aeration diffusers and vacuum chuck plates, sintered porous sheet is produced from 4112 F by compression moulding a dry blend of polymer powder and water-soluble porogen. Sodium chloride or potassium carbonate with a sieved particle size of 5–50 µm is mixed at 25–40 wt% into the UHMW-PE powder in a low-shear tumble blender for 20–40 min. The blend is compacted in a steel mould at 20–30 MPa and heated to 180–210 °C. Sintering time for a 10–20 mm thick sheet is 90–150 min; thicker sections require an additional 10–15 min per 10 mm of thickness. The mould is cooled under pressure at 5–10 °C/min to below 60 °C. Porogen is leached in water at 60–80 °C for 4–8 h, and the sheet is dried at 80 °C to constant mass. The resulting porosity falls between 30 % and 45 %, with a bubble point between 20 kPa and 80 kPa for pore sizes of 5–50 µm as measured by ASTM F316-03. Terminal components include fine-bubble aeration discs, air bearings, and vacuum chuck plates. Continuous service is limited to 80 °C under mechanical load because creep resistance of porous UHMW-PE is lower than that of solid sections. Oxidation degradation is minimised by maintaining sintering temperature below 210 °C and by using an inert gas blanket in the mould cavity. Yellowing or brown discolouration indicates chain scission and loss of tensile strength. There is no harmonised EU standard specific to sintered porous UHMW-PE aeration plates; performance is defined by bubble point and pore size distribution data rather than a single material standard.
Thick-section compression moulding of 4112 F for slurry pump liners and hopper discharge inserts requires a two-stage heating profile to avoid internal porosity. Powder is preheated to 100–120 °C in an air-circulating oven and charged into a preheated mould. A processing stabiliser is dry-blended at 0.05–0.10 wt% when furnace residence time is expected to exceed 60 min. Compaction pressure is applied at 25–40 MPa while the mould is heated to 200–220 °C. The soak time at peak temperature is 10–15 min per 10 mm of section thickness. Cooling under pressure is performed at 5–10 °C/min until the core temperature reaches 40 °C. For sections thicker than 40 mm, mould pressure is released incrementally at 10 MPa steps to prevent void formation from differential shrinkage. The primary failure mode is oxidative degradation at the mould surface; this is controlled by maintaining oxygen content below 1 % in the heating chamber and by limiting peak temperature to 220 °C. The resulting slabs are machined into abrasion liners for mineral slurry transfer chutes, pump intake boxes, and chain wear strips. Abrasion performance is evaluated under ASTM G65-16 Procedure A; impact resistance is tested under ISO 179-1/1eA. The continuous operating PV value for slurry-lubricated sliding against carbon steel is typically below 0.05 MPa·m/s; abrasive particle size above 0.5 mm reduces the permissible PV limit further. Service temperature under abrasive load is limited to 80 °C. Published data for this specific 4112 F configuration in thick-section compression moulding are limited; core porosity and shrinkage must be verified by ultrasonic inspection or sectioning on the first production batch.
Water-lubricated marine bearing staves machined from 4112 F require post-sintering stress-relief annealing to maintain dimensional stability in seawater service. The starting slab is compression moulded from neat powder at 200–220 °C and cooled under pressure. After rough machining to an oversize of 1–2 mm, the staves are annealed in air at 100–110 °C for 2 h per 25 mm of thickness and cooled at 0.5–1.0 °C/min. This step reduces residual stress from the moulding cycle and prevents warping during final CNC machining. Final dimensions are held to a tolerance of ±0.05 mm for bearing shell segments. Water absorption is below 0.01 % by mass after 24 h immersion in seawater at 23 °C; dimensional change in water is negligible compared with nylon bearing materials. The staves operate as water-lubricated bearings on ship propeller shafts and pump shafts, where seawater provides cooling and lubrication. Coefficient of friction against stainless steel at 0.05 MPa bearing pressure and 0.5 m/s surface speed is below 0.15. The permissible PV limit in seawater is typically 0.01–0.03 MPa·m/s; exceeding this limit causes local heat accumulation and bearing surface melting due to the low thermal conductivity of UHMW-PE. Marine classification society requirements, such as DNV or ABS approval, apply to the finished bearing assembly rather than the raw polymer slab. Published data for 4112 F in water-lubricated marine service are limited; long-term swelling and creep tests in seawater should be generated for the specific bearing geometry before classification submission.
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