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ExxonMobil Exceed LLDPE 1001BU

    • Product Name: ExxonMobil Exceed LLDPE 1001BU
    • Factroy Site: Yudu County, Ganzhou, Jiangxi, China
    • Price Inquiry: admin@ascent-chem.com
    • Manufacturer: Ascent Petrochem Holdings Co., Limited
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    Specifications
    HS Code 937581
    Product ExxonMobil Exceed LLDPE 1001BU
    Resin Type Metallocene Linear Low Density Polyethylene (mLLDPE)
    Comonomer Hexene
    Density 0.918 g/cm³
    Melt Flow Rate 190 C 2 16 Kg 1.0 g/10 min
    Melting Point Dsc 118 °C
    Crystallization Point Dsc 104 °C
    Vicat Softening Temperature 102 °C
    Tensile Strength At Yield 9.0 MPa
    Tensile Strength At Break 44 MPa
    Elongation At Break 690%
    Flexural Modulus 260 MPa
    Shore D Hardness 55

    As an accredited ExxonMobil Exceed LLDPE 1001BU factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing ExxonMobil Exceed LLDPE 1001BU is supplied as free-flowing pellets in 25 kg polyethylene bags, providing safe handling and storage.
    Container Loading (20′ FCL) 20′ FCL container loading of ExxonMobil Exceed LLDPE 1001BU: palletized bags, properly secured, ensuring safe, efficient ocean transport.
    Shipping ExxonMobil Exceed LLDPE 1001BU is a non-hazardous linear low-density polyethylene resin shipped in pellet form. It is typically packed in 25 kg bags, bulk bags, or railcars. Transport via dry containers or covered trucks, protected from moisture, heat, and direct sunlight. No hazmat restrictions apply.
    Storage Store ExxonMobil Exceed LLDPE 1001BU in a dry, cool, well-ventilated area away from direct sunlight, heat sources, and oxidizing agents. Keep containers tightly sealed when not in use to prevent contamination and moisture pickup. Ensure proper grounding to avoid static discharge. Avoid stacking excessively high to maintain pellet integrity and safe handling.
    Shelf Life Shelf life is indefinite when stored in a dry, cool area, away from direct sunlight and contaminants.
    Application of ExxonMobil Exceed LLDPE 1001BU

    On blown-film lines producing heavy-duty shipping sacks and industrial liners in thicknesses from 50 µm to 125 µm, ExxonMobil Exceed 1001BU is converted on grooved-feed extruders with barrier screws having L/D ratios of 24:1 to 30:1, coupled to spiral mandrel dies with die gaps of 1.5 mm to 2.0 mm. The resin is an ethylene-hexene copolymer with density 0.918 g/cm³ measured under ASTM D1505 and melt index 1.0 g/10 min under ASTM D1238 at 190 °C and 2.16 kg. Melt temperature at the die inlet is maintained from 195 °C to 225 °C, while blow-up ratio is kept from 2.0:1 to 3.0:1 and frost line height from 4 die diameters to 6 die diameters. Frost line distances beyond 8 die diameters reduce transverse-direction tear resistance measured under ASTM D1922 and produce visible bubble sway. Fluoropolymer processing aid masterbatch is dosed at 0.02 wt% to 0.05 wt% to suppress melt fracture; slip packages are held below 0.10 wt% to avoid depression of heat seal strength measured under ASTM F88. Calcium carbonate filler above 2 wt% is incompatible with this sack structure because dart impact under ASTM D1709 Method A decreases and seal-corner stress concentrations increase. Regulatory compliance for food ingredient sacks is based on FDA 21 CFR §177.1520 and EU Regulation (EU) No 10/2011, with finished-article migration testing required because resin-grade compliance does not certify laminated or printed structures. Terminal products include bulk resin shipping sacks, fertilizer bags, and industrial bin liners in which dart impact, tear propagation, and top-load seal integrity are release criteria.

    The main processing conflict in this segment is the interaction between die gap and melt temperature at high screw speeds. When die gap is reduced to 1.2 mm to improve gauge uniformity, shear stress in the die land rises and may exceed the critical shear stress of metallocene LLDPE, producing sharkskin melt fracture that is not completely suppressed within the allowable processing-aid dosage range. Elevating melt temperature above 230 °C to reduce viscosity increases thermal oxidation risk, and gel counts recorded by automated optical film inspection rise after residence times longer than 6 min. Decreasing melt temperature below 190 °C raises back pressure at the grooved-feed section, causing screw speed fluctuations that generate gauge bands of ±4% at an 80 µm target thickness. Dual-lip air rings and internal bubble cooling at 10 °C to 15 °C are used to stabilise the bubble neck and permit higher throughput without frost-line excursions. In production halls above 80% relative humidity, cold pellet surface moisture produces pinholes and bubble instability; hopper throat temperature is set to 40 °C to 50 °C or a desiccant hopper is specified.

    What Limits Pinhole Formation in 20 µm Frozen Food Packaging Film?

    Frozen food packaging film based on 1001BU is commonly converted at 20 µm to 25 µm gauge in monolayer or coextruded structures in which the sealant layer contains 100 wt% 1001BU. Pinhole formation is limited by bubble stability, contaminant gels, and draw-down ratio. Die gap is set at 1.0 mm to 1.2 mm for thin gauge to increase draw ratio and improve impact strength, but this configuration raises die-head pressure and requires fluoropolymer processing aid at 0.03 wt% to 0.06 wt% to control melt fracture at output rates above 180 kg/h on spiral mandrel dies. Melt temperature is kept from 200 °C to 215 °C; lower temperatures generate crystalline nuclei that survive the frost line and produce pinholes after flex durability conditioning under ASTM F392. The film is evaluated for pinhole density by automated optical film inspection using a 500 mm water column; published data for this specific gauge in frozen-food configurations is limited, and acceptance thresholds are set by the converter after flex durability exposure. Food-contact compliance is governed by FDA 21 CFR §177.1520 and EU Regulation (EU) No 10/2011, with organoleptic migration testing under EN 1186-1 because low-temperature storage does not eliminate all sealant-layer migrants. Terminal products include pillow pouches for vegetables, side-gusseted bags for poultry, and liners for frozen seafood.

    Downstream failures concentrate at the collapsing frame and nip rolls. Blocking at the nip increases when slip additives are reduced to preserve seal performance; diatomaceous earth or synthetic amorphous silica is therefore added at 0.05 wt% to 0.10 wt% in the outer skin, not in the sealant layer, to avoid shifting seal initiation temperature. Overdrying antiblock masterbatch above 80 °C degrades the carrier resin and creates fish eyes that are visible at 20 µm gauge and are recorded by automated optical film inspection. Internal bubble cooling air is filtered to 5 µm to prevent airborne fines from embedding in the molten film. On production-scale lines, upward gel-count trends are correlated with die-lip deposit formation at the frost line and are corrected by die cleaning rather than by increasing melt temperature, because higher melt temperature in this thin-gauge process reduces bubble stability and raises pinhole risk.

    Lamination sealant webs for aluminium foil and metallized polyester are produced with 1001BU as the low-seal-initiation sealant layer. The sealant web is coextruded at 15 µm to 30 µm thickness in three-layer laminates that include tie resin and barrier substrate; seal initiation temperature is measured under ASTM F88 at 0.5 s and 1.0 s dwell. The sealant layer is run at 100 wt% 1001BU because conventional LDPE above 10 wt% raises seal initiation temperature and narrows the hot-tack window. Extrusion uses a 30:1 L/D barrier screw with melt temperature from 210 °C to 230 °C and die gap from 0.8 mm to 1.2 mm. Draw resonance is controlled by maintaining melt temperature above 210 °C and directing an air knife onto the chill roll; chill roll temperature is held at 15 °C to 20 °C. Food-contact laminates require FDA 21 CFR §177.1520 and EU Regulation (EU) No 10/2011; retortable structures are tested under ASTM F2622 for oxygen transmission and ASTM F88 for seal strength after retort at 121 °C for 30 min. Terminal products include stand-up pouches for dry mixes, lidding films for dairy containers, and retortable pouches for ready-to-eat products.

    The critical process limit in laminate sealant webs is seal contamination by low-molecular-weight oxidised fractions. The narrow molecular weight distribution of metallocene LLDPE lowers extractables but also means melt temperature above 240 °C transfers oligomers to the chill roll. These deposits reduce surface tension below 38 mN/m when measured under ASTM D2578 and cause lamination adhesion failure. Corona dosage is set between 2.5 kW·h/m² and 3.5 kW·h/m² for lamination to aluminium, with re-wetting tension checked inline. Aluminium foil above 9 µm requires a tie resin such as an anhydride-modified polyolefin because unfilled polyethylene does not provide sufficient metal adhesion under retort conditions. Batch-to-batch seal-strength variation above ±8% is normally traced to die-lip adjustment or chill-roll speed fluctuation rather than resin variability.

    Agricultural Silage Film UV Stabilization and Antioxidant Limits

    Silage film and agricultural stretch covers produced from 1001BU are formulated as monolayer film at 25 µm to 40 µm thickness with a HALS and antioxidant masterbatch at 0.20 wt% to 0.60 wt%, depending on field exposure periods from 12 months to 24 months. The resin is not supplied with agricultural UV stabilizers, and converter-side additive loading must be matched to latitude and seasonal orientation. HALS below 0.20 wt% leads to premature embrittlement before the storage period ends; retained elongation at break is tested under ISO 527-3 after accelerated weathering under ASTM G154 Cycle 1 or ISO 4892-2 Method A. Blown-film processing uses a 2.5:1 blow-up ratio and melt temperature from 200 °C to 220 °C, with frost line height controlled at 3 die diameters to 5 die diameters because silage film requires high machine-direction tensile strength for wrapping-machine pre-stretch, typically 50 N/50 mm to 70 N/50 mm measured under ASTM D882. Dart impact is tested under ASTM D1709 Method A, tear under ASTM D1922, and oxygen transmission under ASTM D3985 at 23 °C and 0% relative humidity. Compliance is linked to REACH Annex XVII and national agricultural plastic waste collection codes; no restricted heavy metals or substances specified in the masterbatch may be introduced. Terminal products include bale wrap, pit silage covers, and oxygen-barrier underlayers for maize silage.

    The main conversion conflict is UV-stabilizer dispersion. HALS masterbatch added at the feed throat without sufficient mixing forms localized agglomerates that reduce tear strength and create failure sites under wind load. At loadings above 0.40 wt%, side-feeding or pre-compounding is required because single-screw lines without mixing sections are not suitable. The film pre-stretch ratio during baling is set from 1.2:1 to 1.8:1; exceeding that ratio without increasing thickness causes tear propagation at the bale edge and loss of anaerobic conditions. In cold-weather wrapping below 5 °C, film stiffness increases and converter specifications require conditioned dart impact testing at -20 °C; this is the primary failure mode in Nordic storage applications, where retained impact after UV weathering is also specified.

    Application segmentRegulatory frameRelease-critical test methodCritical process condition
    Heavy-duty sacks and industrial linersFDA 21 CFR §177.1520; EU Regulation (EU) No 10/2011ASTM D1709 Method A; ASTM D192250–125 µm gauge; BUR 2.0:1–3.0:1
    Frozen food packagingFDA 21 CFR §177.1520; EU Regulation (EU) No 10/2011ASTM F392; ASTM F88; EN 1186-120–25 µm; 100 wt% 1001BU sealant layer
    Lamination sealant webFDA 21 CFR §177.1520; EU Regulation (EU) No 10/2011ASTM F88; ASTM F2622; ASTM D257815–30 µm sealant layer; retort 121 °C, 30 min
    Agricultural silage filmREACH Annex XVII; national agriplastic collection codesISO 527-3; ASTM G154 Cycle 1; ASTM D3985HALS 0.20–0.60 wt%; pre-stretch 1.2:1–1.8:1
    Collation shrink filmEU Directive 2011/65/EU RoHS; REACHISO 14616; ISO 829510±2 wt% LDPE blend; shrink 15–30%
    Cast film and hygiene backsheetFDA 21 CFR §177.1520; EU Regulation (EU) No 10/2011; REACH candidate listISO 8295; automated optical film inspectionLayer ratio 20–30 wt% 1001BU; die gap 0.5–0.8 mm

    When Dry-Blending 1001BU with 10 wt% LDPE for Collation Shrink Film

    When 1001BU is dry-blended with 10 wt% high-pressure LDPE for collation shrink film, the film is processed at 35 µm to 50 µm thickness on blown-film lines with die gaps of 1.2 mm to 1.5 mm and blow-up ratios from 2.0:1 to 2.5:1. The LDPE component modifies bubble stability and increases transverse-direction shrink but reduces dart impact; the blend ratio is held at 10±2 wt% because LDPE above 20 wt% lowers dart impact under ASTM D1709 Method A and widens the heat-seal initiation range. Film orientation is controlled by frost-line height and let-off speed, then the sleeve is processed in a hot-air shrink tunnel at 130 °C to 150 °C. Shrink percentage is measured under ISO 14616 at 120 °C in both machine and transverse directions. Melt temperature is set from 210 °C to 225 °C, which is 10 °C to 20 °C above monolayer heavy-duty sack film settings to reduce residual stress memory and tunnel-induced edge curl. Regulatory compliance for beverage multipacks requires slip testing under ISO 8295 and excludes heavy metals or phthalates above the limits of EU Directive 2011/65/EU RoHS because the product enters retail packaging streams. Terminal products include bottle bundles, can multipacks, and box over-wrap that requires controlled shrinkage from 15% to 30%.

    Uneven shrink force caused by inconsistent blending is the main process bottleneck. Dry tumble blending for less than 15 minutes per batch creates LDPE-rich pockets that produce shrink bands and visible tunnel marks; blending longer than 30 minutes generates fines that can be detected by automated optical film inspection as gel-like defects. Gravimetric feeding of both resins into the extruder throat at a combined rate control of ±1% is preferred. In-line shrink force is monitored with a shrink film tensiometer in both machine and transverse directions; deviations above 20% relative to target indicate unstable bubble geometry or incorrect frost-line height. Processing aid above 0.05 wt% is usually unnecessary in this structure and can reduce slip coefficient below 0.15, causing roll blocking during storage. Shrink tunnel residence time longer than 10 s at 150 °C distorts seal areas; the tunnel profile is therefore ramped from 115 °C to 145 °C rather than operated at a single set point.

    Cast film lines equipped with chilled rolls at 15 °C to 25 °C and feedblock slot dies convert 1001BU into 20 µm to 40 µm lamination webs and surface layers for hygiene packaging. The melt index of 1.0 g/10 min is low for cast film, so the resin is not used as the highest-draw skin layer; it is coextruded as a toughness layer at 20 wt% to 30 wt% of a three-layer structure with higher-melt-index metallocene LLDPE skins. Melt temperature at the slot die is set from 230 °C to 245 °C, die gap from 0.5 mm to 0.8 mm, and air-knife pressure from 0.02 MPa to 0.04 MPa. Chill-roll embossing is used to control web flatness and coefficient of friction; slip agent is blended at 0.05 wt% to 0.10 wt% and measured under ISO 8295. Regulatory compliance for hygiene packaging requires FDA 21 CFR §177.1520 and EU Regulation (EU) No 10/2011 for adjacent food-contact layers, plus absence of substances on the REACH candidate list. Terminal products include backsheet films for sanitary pads, lamination films for absorbent products, and industrial surface-protection films.

    Draw resonance at chill-roll speeds above 150 m/min is the limiting constraint. Narrowing the die gap and increasing melt temperature to 235 °C reduces draw resonance, but residence time above 8 minutes at that temperature generates oxidative gel recorded by automated optical film inspection. Cast film produced from 1001BU is not recommended for high-speed stretch wrapping because the low melt index and higher crystallinity at the chill roll result in insufficient cling after winding; published data for this specific cast film configuration is limited, and converter trials are required before substituting higher-melt-index cast grades.

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    Certification & Compliance
    More Introduction

    ExxonMobil Exceed LLDPE 1001BU is a metallocene-catalysed linear low density polyethylene resin supplied in pellet form for blown film conversion. The resin is specified by a nominal density of 0.918 g/cm³ determined according to ASTM D1505 and a nominal melt mass-flow rate of 1.0 g/10 min determined according to ASTM D1238 at 190 °C under 2.16 kg. The equivalent melt mass-flow rate may be reported under ISO 1133-1:2022. These values place the product in the lower-density, moderate-viscosity segment used for film structures requiring a defined balance between melt pumping and draw-down. The grade belongs to the Exceed family, which is characterised by a narrow molecular weight distribution and controlled short-chain branching distribution relative to broad-molecular-weight-distribution Ziegler-Natta LLDPE resins of identical melt index and density.

    Thermal and Rheological Benchmarks Relevant to Film Extrusion

    The resin is ordinarily processed on single-screw blown film extruders with 24:1 to 30:1 length-to-diameter ratios. Barrier screws, Maddock mixing sections, and spiral mandrel dies are common; die gaps in the range 1.8 mm to 2.5 mm and blow-up ratios from 2.0:1 to 3.0:1 are reported in converter screening. Melt temperature is normally controlled between 190 °C and 220 °C at the adapter. Residence times above 5 min should be avoided because thermal oxidation of the polymer can generate gel particles and black specks in stagnant die regions. Because the resin exhibits less shear thinning than a conventional butene LLDPE of equivalent melt index, melt pressure at the die may increase at the same screw speed. The practical consequence is that extruder drives with limited torque or shallow-flighted screws may become the constraint before the resin reaches its maximum stable output.

    The table below lists reported nominal resin properties. Finished film values are dependent on gauge, die geometry, and downstream processing conditions.

    PropertyStandard procedureReported nominal value
    DensityASTM D15050.918 g/cm³
    Melt mass-flow rateASTM D1238, 190 °C/2.16 kg; equivalent to ISO 1133-1:20221.0 g/10 min

    Melt rheological characterisation of metallocene LLDPE of this melt index is typically performed by rotational rheometry under nitrogen at 190 °C and 210 °C. Dynamic frequency sweeps from 0.01 rad/s to 100 rad/s show a low-frequency terminal plateau and a shear-thinning onset at higher frequencies than a broad-molecular-weight-distribution high-pressure LDPE. Capillary rheometry at apparent shear rates of 100 s⁻¹ and 1000 s⁻¹ can be used to compare die pressure predictions. Published data for this specific grade under a standard universal laboratory film is limited; converter-scale trials remain the required method to establish values for a given line.

    Molecular weight distribution influences the shear-thinning exponent of the resin. For a metallocene LLDPE of this nominal melt index, the low-shear viscosity is higher relative to a broad-molecular-weight-distribution LLDPE at equivalent melt index, while the high-shear viscosity is lower. In a single-screw extruder, this means the screw requires more torque in the metering section but may develop less shear heating in the die. The temperature profile should therefore be set to compensate for the reduced viscous heating. A flat profile of 180 °C, 190 °C, 200 °C, 200 °C, 200 °C from hopper to die is a common converter starting point for a 24:1 extruder, but actual temperatures must be adjusted for die size and output.

    What limits bubble stability at low gauge on high-stalk lines?

    Low gauge operation with 1001BU is influenced by the interaction between melt strength and quench rate. In high-stalk configurations, the stalk is cooled by ambient air before the film enters the dual-lip air ring. If the frost-line height is set too low relative to the die diameter, the film may leave the air ring with a high surface temperature and the bubble can oscillate. If the frost-line height is set too high, draw resonance and gauge variation may increase. The metallocene molecular weight distribution of the resin produces a narrower processing window for bubble stability than a broad-molecular-weight-distribution autoclave LDPE. Converters often adjust internal bubble cooling, air ring lips, and die temperature profile to manage the metastable region. On 50 mm to 65 mm extruders with spiral mandrel dies, gauge bands below 25 µm may require secondary air support and higher blow-up ratios.

    Surface melt fracture, also called sharkskin, can appear at the die lip when the melt wall shear stress exceeds a critical level. The metallocene narrow molecular weight distribution of 1001BU does not generate the same shear-stress relaxation as broad-molecular-weight-distribution autoclave LDPE; the onset of surface melt fracture may therefore occur at lower linear output. On spiral mandrel dies, the defect usually presents as alternating glossy and rough bands. The corrective sequence is to increase die temperature, open the die gap, reduce extruder speed, or add a fluoropolymer processing aid at 0.02–0.05 wt%. Pressure-drop measurements across the adaptor can identify the point at which a process aid has coated the die surface. The die pressure will stabilise after a conditioned period that ranges from 20 min to 60 min depending on die geometry and additive concentration.

    Processing boundaries and resin-handling constraints

    Polyethylene resins of this class do not require the same moisture-drying protocol as PA or PET. However, condensation formed during transfer from cold storage to a warm, humid hopper must be removed; surface moisture can cause feed bridging and output surging. Pellets should be stored below 50 °C and protected from direct ultraviolet exposure during prolonged outdoor storage. The resin is not recommended for continuous service in contact with strong oxidising acids, chlorinated solvents, or aromatic hydrocarbons at elevated temperatures without appropriate barrier protection or chemical resistance testing. Additive concentrates containing high levels of migratory slip or antiblock agents may change the seal initiation temperature and blocking behaviour; the converter should evaluate the final blend on the specific form-fill-seal machine using ASTM F88 and ASTM F2029.

    Food-contact suitability is not self-certified by the processor. Each film structure must be evaluated against 21 CFR §177.1520 or regional food-contact legislation and the supplier’s regulatory compliance certificate. No universal compliance statement applies to all converted articles because the final composition, layer placement, and end-use conditions determine the regulatory status.

    When 1001BU replaces a Ziegler-Natta butene LLDPE in heavy-duty sack film

    The substitution is usually driven by the need to maintain dart impact and tear resistance while reducing film gauge. A metallocene LLDPE of 0.918 g/cm³ density and 1.0 g/10 min melt index will normally provide higher ASTM D1709 dart impact per unit thickness than a conventional Ziegler-Natta butene LLDPE of the same nominal density and melt index. The trade-off is that processability may be lower on older extruders with 18:1 L/D and general-purpose screws; the narrow molecular weight distribution can increase backpressure, reduce shear-insensitive pumping efficiency, and promote melt fracture at lower output. In such conversions, die gaps are typically opened to at least 2.0 mm, barrel profiles are flattened, and fluoropolymer processing aid masterbatch is introduced at 0.02–0.05 wt% to suppress surface defects. The decision to replace a butene LLDPE should be validated by a line trial that records motor load, die pressure, bubble stability, gauge uniformity, and ASTM D1922 tear values in both machine and transverse directions.

    Film toughness testing of structures based on this resin is normally performed by ASTM D1709 dart impact, ASTM D1922 Elmendorf tear, and ASTM D5748 puncture resistance. The comparative advantage of metallocene LLDPE is most visible in lower-gauge films because the homogeneous distribution of short-chain branches reduces the population of low-tie-molecule regions that become initiation sites for dart impact failure. This statement is not specific to one film line: orientation levels created by frost-line height, blow-up ratio, and die gap control the crystalline morphology and therefore the final property balance. Direct comparison between blown and cast films is invalid because orientation states differ significantly.

    Compared with high-pressure LDPE of 0.918 g/cm³ density and 0.3 g/10 min melt index, 1001BU has lower melt strength and should not be considered a drop-in for high-stalk bubble stability in shrink film. Blending with high-pressure LDPE at 10–30 wt% is common to improve bubble stability and melt relaxation, but the exact ratio depends on die geometry and frost-line height. The resulting blend must be recharacterised for seal initiation and dart impact because the addition of LDPE alters the crystalline network and the tear resistance of the film.

    In coextruded films, 1001BU is often used as a sealant skin because the narrow composition distribution can deliver a lower seal initiation temperature than standard butene LLDPE, as measured by ASTM F2029. The seal strength after cooling is then verified by ASTM F88. When it is combined with an EVA or polyolefin plastomer sealing layer, the blend ratio must be tuned against blocking and coefficient of friction; no published universal ratio applies. In heavy-duty shipping sacks, industrial liners, frozen food packaging, and agricultural silage films, the resin’s use is supported by converter-generated data rather than laboratory minimums. The final extrusion parameters should be set on the actual line because die geometry, air ring condition, and downstream winding tension interact with the viscoelastic response of the metallocene LLDPE.

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