| HS Code | 291989 |
| Density | 0.93 g/cm³ |
| Molecularweight | 2.5 million g/mol |
| Viscositynumber | 1950 ml/g |
| Bulkdensity | 0.45 g/cm³ |
| Meltingpoint | 135 °C |
| Crystallinity | 45% |
| Tensilemodulus | 700 MPa |
| Tensilestrengthatbreak | 20 MPa |
| Elongationatbreak | 350% |
| Charpynotchedimpactstrength | 100 kJ/m² |
| Shoredhardness | 60 |
| Abrasionresistance | 90 mm³ |
| Coefficientoffriction | 0.15 |
| Waterabsorption | <0.01% |
| Thermalconductivity | 0.41 W/m·K |
| Vicatsofteningtemperature | 80 °C |
| Heatdeflectiontemperature | 45 °C |
| Dielectricstrength | 45 kV/mm |
| Volumeresistivity | 10^17 Ω·cm |
As an accredited Celanese UHMW-PE X 195 factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Celanese UHMW-PE X 195 is packaged in 25 kg polyethylene-lined paper bags, palletized and shrink-wrapped for industrial shipping. |
| Container Loading (20′ FCL) | Celanese UHMW-PE X 195: palletized packages loaded into a 20′ FCL container, securely strapped, evenly distributed, moisture-protected, and labeled for transport. |
| Shipping | For transport, Celanese UHMW-PE X 195 is generally classified as non-hazardous and not regulated by DOT/IATA/IMDG. Use clean, dry, sealed containers. Protect from moisture, contamination, and ignition sources; avoid dust generation. No UN number, class, packing group, or marine pollutant label required. |
| Storage | Store Celanese UHMW-PE X 195 in a cool, dry, well-ventilated area, away from heat, sparks, flames, and strong oxidizers. Keep containers tightly closed to prevent moisture and dust contamination. Avoid generating or accumulating dust; use grounding and bonding when handling powder. Protect from direct sunlight and store only in original or compatible containers. Follow local regulations and the SDS. |
| Shelf Life | Store in original packaging in a dry place below 30°C; shelf life at least 2 years. Protect from direct sunlight. |
| Formulation Parameter | Unit | Range | Measured Output Variable | Test Method |
|---|---|---|---|---|
| UHMW-PE X 195 loading | wt% | 25–35 | Gel viscosity | Capillary rheometry, 190°C |
| Stretch ratio (MD × TD) | — | 5×5 to 9×9 | Porosity | ASTM D2873, mercury intrusion |
| Thermal setting temperature | °C | 118–128 | Shrinkage at 105°C/1 h | ASTM D1204 |
| Extraction bath residence | s | 30–120 | Residual oil | FTIR, solvent reflux |
| Cumulative Draw Ratio | Filament Diameter (µm) | Tenacity (GPa) | Elastic Modulus (GPa) |
|---|---|---|---|
| 10× | 28–32 | 1.2–1.6 | 30–50 |
| 30× | 18–22 | 2.2–2.8 | 70–100 |
| 60× | 12–15 | 3.2–3.8 | 120–150 |
| 80× | 8–11 | 3.6–4.2 | 140–170 |
Competitive Celanese UHMW-PE X 195 prices that fit your budget—flexible terms and customized quotes for every order.
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Celanese UHMW-PE X 195 is an ultra-high-molecular-weight polyethylene homopolymer supplied as a white free-flowing powder. The model designation X 195 corresponds to a nominal viscosity number in the 1900–2000 cm³/g region, with a manufacturer reference point of 1950 cm³/g measured according to ISO 1628-3 in decahydronaphthalene at 135 °C. Representative lot data also identify a density of 0.93 g/cm³ by ISO 1183-1 and a peak melting temperature of 130–136 °C by ISO 11357-3. Because the polymer does not exhibit a measurable melt flow rate under ISO 1133-1:2022, conventional injection moulding is not applied to this grade. Processing is instead conducted by compression moulding, ram extrusion, or oil-assisted twin-screw extrusion for gel films and porous structures.
In wet-process lithium-ion battery separator manufacture, X 195 is dry-blended with hydrocarbon oil or paraffin oil at oil-to-polymer ratios between 70:30 and 80:20. The slurry is introduced to a counter-rotating twin-screw extruder with an L/D ratio of 40:1 or greater and a gear melt pump before a flat T-die. The cast gel sheet is cooled, extracted, and biaxially stretched at temperatures below the polymer melting point. The high solution viscosity of X 195 raises gel-stage modulus and permits higher machine-direction orientation ratios, commonly 4:1 to 6:1, while transverse-direction stretching is normally limited to 1.5:1 to 3:1 during the first pass. Production-scale data for membranes below 5 µm are lot-specific; published data for this specific configuration are limited and should not replace pilot-line validation.
For gel-spun fibre and tape trials, X 195 has been evaluated at solution concentrations of 5–10 wt% in decalin or mineral oil. The solution is extruded through a spinneret at 130–160 °C, quenched, and drawn to total draw ratios above 30:1. In these configurations, the viscosity number of X 195 increases spinning-line tension and can widen the draw resonance band if the die-to-bath air gap is longer than 20 mm. Published correlations between this specific grade and final fibre tenacity are limited; most gel-spinning process data are generated on dedicated pilot lines with closed-loop tension control rather than on standard separator equipment.
Compared with grades in the 1500–1700 cm³/g viscosity range, X 195 develops a more elastic gel network during oil swelling. This difference supports higher draw ratios before pore-flattening defects appear, but it also raises the specific mechanical energy input to the twin-screw line. Process operators report that torque increases of approximately 10–20 % occur when a 1500 cm³/g reference powder is replaced by a 1950 cm³/g powder at identical feed rate and screw speed. The same substitution can lower throughput when the extruder drive or melt pump suction pressure reaches nameplate limits. The material therefore should not be considered a drop-in replacement for lower-viscosity GUR powders without reviewing feeder capacity, extruder drive sizing, and die-pressure control.
Dry blending of X 195 with internal lubricants and antioxidants is usually performed in a high-speed mixer at tip speeds below 25 m/s to avoid powder fibrillation and local melting. The blend is metered with a loss-in-weight feeder fitted with twin concave screws. Segregation and compaction in the hopper become process risks when the powder bulk density falls below 0.38 g/cm³ or when the D90 size exceeds 300 µm. The manufacturer's normal lot envelope for bulk density is 0.40–0.46 g/cm³ by ISO 60, with a median particle size of 120–160 µm by ISO 13320. If the powder is stored at relative humidity above 60 % and then transferred into a cold production hall, condensation can create surface defects in compression-moulded parts. Drying at 80 °C for 2–4 h before closed-mould processing removes this boundary moisture without altering molecular weight.
In compression moulding, the powder is charged into a closed mould and consolidated at 5–10 MPa, then heated above the crystalline melting region to 200–220 °C. Dwell time is typically 10–30 min per 10 mm of plaque thickness, followed by controlled cooling at 10–15 °C/min to reduce internal stress and prevent weld-line porosity. X 195 has a longer particle coalescence time than lower-viscosity UHMW-PE grades; incomplete sintering appears as microvoids and reduced double-notch impact resistance. In ram extrusion, the powder is compacted by a reciprocating ram through a heated die with zone temperatures from 180 °C near the feed chamber to 240 °C in the die land. The extruded stock is used for chain guides, wear strips, star wheels, and skived sheets. Prolonged exposure above 250 °C is not recommended because thermal-oxidative chain scission accelerates and surface yellowing may occur.
Mechanical property expectations for compression-moulded test plaques prepared following ISO 11542-2 include tensile yield stress of 20–23 MPa, elongation at break above 300 % by ISO 527-2/1B, and Shore D hardness of 62–66 by ISO 868. The product's notched Charpy impact resistance at 23 °C generally returns a non-break result under ISO 179-1. These values are typical for UHMW-PE homopolymers of this viscosity class and are not guaranteed lot-release values. In machined parts, the high coefficient of linear thermal expansion, approximately 1.5–2.0 × 10⁻⁴ K⁻¹, must be accommodated through expansion joints or operating-temperature limits.
In sintered porous parts, the powder is compacted at low pressure and heated to 200–220 °C for time intervals determined by section thickness. Porosity is created by controlled particle packing rather than by chemical blowing agents. The residual ash below 100 ppm reduces ionic contamination in battery or filtration environments where extractable metal species are limited by the end-use specification. Narrow particle size distribution improves pore-size uniformity after sintering, but batch-to-batch differences in D10 and D90 must be monitored because changes in fine-particle fraction alter the capillary pressure required for uniform liquid penetration.
| Property | Typical value or range | Test method |
|---|---|---|
| Viscosity number | 1950 cm³/g | ISO 1628-3 |
| Density | 0.93 g/cm³ | ISO 1183-1 |
| Melting peak temperature | 130–136 °C | ISO 11357-3 |
| Bulk density | 0.40–0.46 g/cm³ | ISO 60 |
| Median particle size D50 | 120–160 µm | ISO 13320 |
| Ash content | <100 ppm | ISO 3451-1 |
| Tensile yield stress | 20–23 MPa | ISO 527-2 |
| Elongation at break | >300 % | ISO 527-2 |
| Shore D hardness | 62–66 | ISO 868 |
Compliance status is application-dependent. The following matrix identifies the standards and regulations most frequently referenced for this grade family. Final conformity must be verified by the converter on the finished article because polymer lot data alone do not establish regulatory clearance.
| Standard or regulation | Relevance to X 195 applications |
|---|---|
| REACH Regulation (EC) No 1907/2006, Article 33 | Supply-chain SVHC confirmation required for articles sold in the EU; the polymer substance as such is generally exempt from registration, while monomers and additives may require registration. |
| RoHS Directive 2011/65/EU, Annex II | Applies to electrical and electronic equipment; the polymer matrix must not contain restricted substances above homogeneous material limits. |
| FDA 21 CFR 177.1520 | Olefin polymer food-contact clearance; requires end-testing for extractives and formulation conformance for specific use temperatures. |
| ASTM F648-21 and ISO 5834-2 | Ultra-high-molecular-weight polyethylene powder and consolidated forms for surgical implants; not all lots are automatically released for implant use. |
| ISO 10993-1 | Biocompatibility evaluation for medical devices; material identity alone is not sufficient to establish biological safety. |
Machining of X 195 stock requires carbide or polycrystalline diamond tooling with aggressive chip clearance. Cutting speeds above 500 m/min without adequate coolant can melt the cut surface and create a hazy, degraded zone. Hot-plate welding at 200–220 °C is preferred over ultrasonic welding for large assemblies because the melt does not flow readily; ultrasonic energy may eject the molten layer before a uniform weld bead forms. Storage in sealed containers below 30 °C, protected from ultraviolet light and oxidizing agents, is recommended. Under these conditions, the viscosity number and powder flow properties are typically unchanged for 36 months from the certificate date.
Compared with extrudable HDPE grades such as pipe resins, X 195 does not provide the same melt-processability or weld-line strength in injection-moulded parts; its value is in wear life, impact resistance, and solvent-assisted film forming. Compared with lower-molecular-weight UHMW-PE powders used in general wear parts, X 195 may exhibit a measurable improvement in sand-slurry abrasion resistance and a reduction in fatigue cracking, but the difference is not linear and depends on sintering quality. Comparative wear data should be generated according to ASTM G75 or ISO 15527 for the actual tribological system. Processors who currently use a 1500 cm³/g or 1700 cm³/g powder should not assume that upgrading to this grade will independently improve finished-part properties if the sintering or stretching equipment cannot accommodate the higher torque and longer dwell times.