| HS Code | 570279 |
| Density | 0.918 g/cm³ |
| Melt Flow Rate | 1.0 g/10 min |
| Tensile Strength At Yield Md | 11.6 MPa |
| Tensile Strength At Yield Td | 10.3 MPa |
| Tensile Strength At Break Md | 36.5 MPa |
| Tensile Strength At Break Td | 31.0 MPa |
| Elongation At Break Md | 350% |
| Elongation At Break Td | 650% |
| 1 Secant Modulus Md | 160 MPa |
| 1 Secant Modulus Td | 190 MPa |
| Dart Drop Impact F50 | 130 g |
| Elmendorf Tear Strength Md | 220 g |
| Elmendorf Tear Strength Td | 320 g |
| Puncture Force | 5.0 N |
| Haze | 9% |
| Gloss 45 | 12 |
| Melting Point Dsc | 121°C |
| Vicat Softening Point | 100°C |
| Brittleness Temperature | -75°C |
As an accredited ExxonMobil LLDPE LL1001XBU factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | ExxonMobil LLDPE LL1001XBU is supplied as pellets in 25 kg bags, ensuring safe handling and easy processing. |
| Container Loading (20′ FCL) | 20′ FCL loading of ExxonMobil LLDPE LL1001XBU resin pellets, packed in FIBC bags, secured for safe transport. |
| Shipping | ExxonMobil LLDPE LL1001XBU ships as non-hazardous polyethylene resin in pellet form. Transport in clean, dry containers or FIBC bags, protected from moisture and direct sunlight. Avoid exposure to high heat and sharp objects. Not classified as dangerous goods under IMO/ADR regulations. Ensure proper labeling and segregation from incompatible materials. |
| Storage | Store ExxonMobil LLDPE LL1001XBU in a clean, dry, well-ventilated area, away from direct sunlight, heat sources, and ignition sources. Keep packaging sealed to prevent moisture pickup and contamination. Maintain moderate ambient temperatures and avoid stacking excessively high to prevent pellet deformation. Use first-in, first-out rotation; shelf life is typically one year. |
| Shelf Life | Shelf life is typically 1 year when stored unopened in original packaging in a dry, cool, shaded environment. |
| Requirement | Test method | Condition | Acceptance value |
|---|---|---|---|
| US FDA direct food contact | 21 CFR 177.1520(c) | Olefin polymer specification | Verify density and extractables per regulation |
| EU overall migration | EN 1186-14 | 10 days at 40 °C, simulant per food type | ≤ 10 mg/dm² |
| EU specific migration of 1-hexene | EN 13130-1 | Annex I SML assignment in EU 10/2011 | ≤ prescribed SML value |
| Packaging heavy metals | EN 14582 | Digestion and ICP-OES | Sum Pb, Cd, Hg, Cr VI < 100 mg/kg |
| Cold-temperature flex crack | ASTM F392 | 1000 cycles at -20 °C | ≤ 10 pinholes/300 cm² |
| Seal strength for frozen food film | ASTM F88/F88M | 300 mm/min, 25 mm specimen | ≥ 22 N/25 mm for 60 µm film |
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ExxonMobil LLDPE LL1001XBU is a linear low-density polyethylene resin supplied in pellet form for blown-film extrusion. The nominal melt mass-flow rate is 1.0 g/10 min at 190 °C under 2.16 kg when determined to ISO 1133-1 or ASTM D1238, and the nominal density is 0.918 g/cm³ at 23 °C by ISO 1183 or ASTM D1505. These values are typical lot-average values rather than batch-release specifications; the certificate of analysis governs each shipment. The resin is positioned for general-purpose monolayer and coextruded blown film where a balance of drawdown, dart impact, seal initiation, and film-surface behavior is required. The LL1001 series is conventionally associated with butene-copolymer LLDPE chemistry, but the exact comonomer identity, molecular architecture, and stabilizer package should be verified against the supplier’s current product datasheet and lot-specific certificate of analysis.
For resin classification under ISO 1043, the material falls within the polyethylene family as a linear low-density grade. It is not a high-pressure low-density polyethylene homopolymer, nor a hexene- or octene-based higher alpha-olefin LLDPE. The supplier’s published data for this specific XBU additive configuration is limited for some film test conditions; converters should obtain verified film property values from extrusion trial reports rather than extrapolating from general LLDPE class data. The product is intended for conversion on single-screw and high-output grooved-barrel blown-film lines, although equipment-specific setup is required because bubble stability and melt-pressure response differ from high-pressure LDPE.
Processing is typically conducted on single-screw extruders with L/D ratios of 24:1 to 30:1, using barrier screws or purpose-designed LLDPE screws. Barrel-temperature profiles commonly begin at 160 °C to 180 °C in the feed zone and ramp to 210 °C to 240 °C at the die. Because LLDPE is more shear-thinning than high-pressure LDPE but less shear-thinning than metallocene plastomers, the observed melt temperature can be 5 °C to 15 °C higher than the set point under high screw speed due to viscous dissipation. Die-pressure readings should be trended continuously; a rising pressure at constant output may indicate additive build-up or melt fracture precursors at the die lip.
The die-gap range for conventional blown-film lines is 1.5 mm to 2.5 mm, with spiral mandrel dies of 100 mm to 450 mm diameter on production-scale machines. Blow-up ratios of 2.0:1 to 3.0:1 and frost-line heights of 6 to 10 die diameters are typical starting points. A lower frost line increases quench rate and can improve optical clarity, but may freeze in molecular orientation and raise machine-direction shrinkage. A higher frost line can improve bubble stability at high output, but may reduce film clarity and increase film-width variation. Asymmetric air-ring flow at blow-up ratios above 2.5:1 can produce gauge variation greater than ±5%, which is difficult to correct without reducing line speed or adjusting die centering.
Sharkskin melt fracture is a critical limitation at elevated output. The onset wall shear stress for polyethylenes is generally on the order of 0.2 MPa to 0.4 MPa, although the exact threshold depends on molecular weight distribution and die geometry. On production lines, sharkskin appears as a regular surface roughness perpendicular to film flow. When melt fracture occurs, the first responses are widening the die gap, reducing screw speed, or adding a fluoropolymer processing aid at 200 ppm to 800 ppm. Internal bubble cooling can increase output without exceeding melt-fracture limits, but alters the heat-transfer balance and requires recalibration of frost-line height and air-ring settings. Line operators often note that LL1001XBU reaches a stable bubble more quickly than high-pressure LDPE of similar melt index after startup, but the bubble may be more sensitive to sudden changes in ambient air circulation.
Barrel residence time above 260 °C should be avoided to limit gel formation, off-odor, and additive degradation. During temporary shutdown, the screw should be kept at reduced speed or the barrel temperature lowered; thermal soaking at full processing temperature can degrade stagnant resin in the die and feed sections. Start-up purging with a low-viscosity LDPE or a dedicated purging compound is preferable to extended dry running.
Differentiation from unmodified LLDPE grades in the same density and melt-flow envelope is primarily observed in the formulated additive package and resulting film-surface properties. The XBU designation refers to the specific stabilization and additive configuration supplied with the base resin; it may include slip and antiblock additives at levels established for high-speed film conversion. In contrast to a base resin without antiblock, film produced from formulated grades typically shows higher surface roughness, lower coefficient of friction, and improved winding behavior on high-speed bag machines. Precise additive concentrations are lot-specific and are documented in the certificate of analysis; they are not normally specified as a single fixed value. When a converter runs a non-slip, non-antiblock LLDPE at identical thickness, winder tension settings, gusseting board friction, and die-lip cleanout interval can shift measurably. These differences are surface-additive effects rather than polymer backbone changes, so tensile and dart-impact properties may remain comparable while coefficient of friction and blocking behavior differ.
Compared with high-pressure LDPE of similar 1.0 g/10 min melt flow, LL1001XBU can allow downgauging because the linear architecture generally provides higher tensile strength and dart impact at equivalent thickness. However, bubble stability under high-stalk conditions may be lower than with tubular LDPE because long-chain branching is absent. Internal bubble cooling, a lower blow-up ratio, or a more conservative frost-line height may be required. Compared with medium-density polyethylene or high-density polyethylene film resins, LL1001XBU has lower stiffness and lower water-vapor barrier contribution, but typically better dart impact and clarity in monolayer packaging. Compared with hexene- or octene-based higher alpha-olefin LLDPE grades, the product may offer a different balance of optics, stiffness, and tear performance; if maximum dart impact or Elmendorf tear is the primary requirement, a higher alpha-olefin grade should be evaluated in parallel.
Published datasheet values for monolayer film properties at 25 µm thickness, 2.5:1 blow-up ratio, and 0.8 mm to 2.0 mm die gap are not uniformly reported across jurisdictions; converters should request extrusion trial data from the supplier. Typical values for blown films in the 0.918 g/cm³ density and 1.0 g/10 min melt-flow class are measured using ASTM D882 or ISO 527-3 for tensile properties, ASTM D1922 or ISO 6383-2 for tear resistance, and ASTM D1709 or ISO 7765-1 for impact. Coefficient of friction is determined by ISO 8295 or ASTM D1894. Haze is measured according to ASTM D1003 or ISO 14782; surface-additive packages can increase haze relative to the base polymer but reduce roll blocking and improve packaging-machine performance.
| Property | Method | Nominal value |
|---|---|---|
| Melt mass-flow rate, 190 °C / 2.16 kg | ISO 1133-1 / ASTM D1238 | 1.0 g/10 min |
| Density at 23 °C | ISO 1183 / ASTM D1505 | 0.918 g/cm³ |
| Peak melting temperature, DSC | ISO 11357-3 / ASTM D3418 | 121 °C–125 °C class range |
| Physical form | Visual inspection | Pellets, free of foreign matter |
The table values are nominal lot-averaged resin properties, not film specifications. Film tensile strength, elongation, tear, dart impact, haze, gloss, and coefficient of friction depend strongly on die gap, blow-up ratio, frost-line height, cooling-air temperature, and film thickness. A change in frost-line height of only 2 die diameters can shift dart impact by more than 10% at constant gauge. Direct comparison of film data between laboratories requires identical sample preparation, conditioning at 23 °C ± 2 °C and 50% ± 10% relative humidity, and identical test method revision. Published data for this specific XBU configuration is limited; film values should not be taken from generic LLDPE tables without confirming the additive package and extrusion conditions.
Cold-temperature packaging suitability is assessed by impact testing at target storage temperatures. Polyethylene retains ductility at low temperature, but measured dart impact can decrease by 20% to 50% between 23 °C and -20 °C, depending on film thickness, orientation, and additive content. For freezer films, converters typically specify a minimum dart impact at -20 °C and verify seal strength after filling. The seal-initiation temperature of LL1001XBU is governed by density and comonomer type; lower-density LLDPE grades generally seal at lower temperatures than HDPE or polypropylene. Hot-tack testing should follow ASTM F1921 or an equivalent internal method, because packages filled on vertical form-fill-seal machines can experience seal opening before the seal cools.
Food-contact status is not a single global property. The resin may be supplied to meet FDA 21 CFR 177.1520(c) when used in accordance with the regulation’s conditions for polyolefins. EU food-contact compliance requires a declaration of compliance under Regulation EU 10/2011 and evaluation of migration limits for the complete package. The applicable migration limit depends on the food simulant and contact conditions; converters must obtain the supplier’s food-contact declaration and apply it within the stated end-use limitations. Non-food industrial films do not require these declarations, but the resin may still be sold as a standard commercial grade with no specific food-contact warranty.
| Regulation / standard | Reference | Applicability |
|---|---|---|
| U.S. food contact | FDA 21 CFR 177.1520(c) | Subject to end-use conditions and additive compliance |
| EU food contact | EU 10/2011 | Requires migration testing or worst-case calculation |
| REACH | EC 1907/2006 | Monomer and additive registration obligations |
| RoHS | 2011/65/EU | Applicable to electrical and electronic equipment; supplier declaration required |
Pre-drying is not normally required when pellets are stored in original unopened containers at 20 °C to 30 °C and below 60% relative humidity. If surface condensation occurs, drying in a desiccant hopper at 70 °C to 80 °C for 2 h to 4 h can be used; excessive drying time can oxidize the polymer surface and shift film color or gel level. The resin should not be stored in direct sunlight or near strong oxidizing agents. Incompatibility with certain color concentrates or processing aids can occur when the masterbatch contains unsaturated amides, metal stearates, or incompatible carrier resins that interact with slip and antiblock additives. A controlled trial run should be conducted before introducing a new masterbatch at production scale.
During shutdown, purging with a low-viscosity LDPE or a commercial purging compound is preferable to thermal soaking at full temperature, which can degrade the resin in stagnant zones. Equipment operators should record die pressure, melt temperature, motor load, and line speed during production campaigns; shifts in these variables can identify additive build-up, feed-throat blockage, or melt-homogeneity problems before film defects appear. Lot-to-lot variation in melt mass-flow rate and density is normally small, but changes in additive concentration can occur between production campaigns and should be verified against the certificate of analysis before high-speed packaging trials.