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ExxonMobil Exceed mLLDPE 3518PA

    • Product Name: ExxonMobil Exceed mLLDPE 3518PA
    • Factroy Site: Yudu County, Ganzhou, Jiangxi, China
    • Price Inquiry: sales8@ascent-chem.com
    • Manufacturer: Ascent Petrochem Holdings Co., Limited
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    Specifications
    HS Code 139560
    Productname ExxonMobil Exceed mLLDPE 3518PA
    Polymertype Metallocene Linear Low Density Polyethylene (mLLDPE)
    Catalyst Metallocene
    Comonomer Hexene-1
    Density 0.918 g/cm³
    Meltindex 3.5 g/10 min (190°C/2.16 kg)
    Meltingpoint 119 °C
    Vicatsofteningpoint 96 °C
    Tensilestrengthatyield 10.3 MPa
    Tensilestrengthatbreak 30.3 MPa
    Elongationatbreak 600%
    Flexuralmodulus 241 MPa
    Hardnessshored 50
    Haze 6%
    Gloss 80%
    Dartdropimpact 120 g
    Elmendorftearmd 200 g
    Elmendorfteartd 400 g

    As an accredited ExxonMobil Exceed mLLDPE 3518PA factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing ExxonMobil Exceed mLLDPE 3518PA is supplied in 25 kg polyethylene bags, palletized for secure handling and storage.
    Container Loading (20′ FCL) ExxonMobil Exceed mLLDPE 3518PA loaded in a 20-foot FCL container, palletized bags stowed and secured for ocean shipment.
    Shipping ExxonMobil Exceed mLLDPE 3518PA is a non-hazardous polyethylene resin, typically shipped in moisture-proof bags or bulk containers at ambient temperature. Store and transport protected from moisture, contamination, and direct sunlight; no special dangerous-goods classification is normally required.
    Storage Store ExxonMobil Exceed mLLDPE 3518PA in a cool, dry, well-ventilated area away from direct sunlight, heat, ignition sources, and moisture. Keep in original sealed packaging, prevent contamination and dust, and avoid prolonged UV exposure. Use proper stacking to prevent bag damage. Follow the SDS and local regulations; observe recommended shelf life and inventory rotation.
    Shelf Life Shelf life is 24 months from manufacture when stored in original packaging in a cool, dry, well-ventilated area away from direct sunlight.
    Application of ExxonMobil Exceed mLLDPE 3518PA

    In high-output heavy-duty sack production, the primary processing constraint for ExxonMobil Exceed mLLDPE 3518PA is not barrel temperature but the combination of low melt strength and narrow molecular weight distribution, which produces a small stable bubble window at high blow-up ratios. The resin is an ethylene-hexene copolymer with a density of 0.918 g/cm³ when tested to ASTM D792-20 and a melt index of 3.5 g/10 min under 190°C/2.16 kg loading in ASTM D1238-20. On a three-layer blown film line equipped with a 70 mm grooved-feed extruder with 30:1 L/D, barrel set points of 185°C/195°C/205°C, and die set at 210°C, a melt temperature of 205°C–212°C is maintained for monolayer sack film in the 50–150 µm thickness range. When the die gap is set below 1.8 mm, surface melt fracture appears at the die exit before the frost line, and this fracture is not corrected by raising the melt temperature alone; the use of a fluoropolymer processing aid at 300–600 ppm or widening the die gap to 2.2 mm is required. Blending with LDPE of density 0.924 g/cm³ and melt index 2.0 g/10 min improves bubble stability but introduces a non-linear loss of toughness. A conversion trial on a 25 µm monolayer film at BUR 2.5 and melt temperature 208°C produced the property gradients in Table 1. The critical boundary for heavy-duty sacks is the 40 wt% LDPE addition level: below this level the low-temperature drop resistance of a 25 kg filled sack at -20°C remains acceptable under ISO 7965-1 drop testing, but at 40 wt% LDPE the dart impact value falls below 300 g and the film is vulnerable to palletization failure. Recycle of edge trim containing nylon or EVOH should be limited to 5 wt% because the immiscible barrier phase causes gel-like defects and reduces tear strength.

    Formulation 3518PA/LDPE (wt%)Dart impact ASTM D1709-15 Method A (g)MD tear ASTM D1922-09 (g)TD tear ASTM D1922-09 (g)Haze ASTM D1003-13 (%)Melt pressure at 70 mm extruder (bar)
    100/08202604208.0385
    80/205201702606.5345
    70/303601301906.0315
    60/40240901305.7290

    Table 1 values are typical converter data obtained under the stated extrusion conditions, not product specification limits.

    What governs seal initiation and hot-tack range in retortable stand-up pouch sealant webs?

    The selection of Exceed mLLDPE 3518PA for a stand-up pouch sealant web is governed less by total seal strength than by the hot-tack envelope under ASTM F1921-23, because vertical form-fill-seal machines impose jaw dwell times of 0.3–0.6 s while the filled pack remains under tension. The ethylene-hexene comonomer distribution lowers seal initiation more sharply than butene-based LLDPE of equivalent density. In a 30 µm monolayer sealant film, a seal strength of 2 N/15 mm is typically reached at jaw set points between 95°C and 105°C, at 0.5 s dwell and 0.4 N/mm² sealing pressure. For a conventional LDPE sealant, the same seal strength requires 115°C–125°C. The hot-tack strength at 110°C and 0.5 s dwell is reported in converter trials at 4.0–6.0 N/15 mm, which is above the 3.0 N/15 mm threshold that prevents seal pop-open in a 60 m/min pouch line. The laminate structure for retortable pouches typically uses 12 µm polyester or 15 µm biaxially oriented polyamide as the print web, 9 µm aluminium foil as the barrier, and 30–60 µm 3518PA sealant film as the food-contact layer. For migration compliance, the resin is evaluated under FDA 21 CFR 177.1520(c) for olefin polymers and under EU Regulation No 10/2011 with overall migration limits. The lower temperature boundary of the sealing window is set by insufficient molecular interdiffusion, while the upper boundary is set by melt displacement out of the seal area; at sealing jaw temperatures above 150°C and dwell beyond 0.8 s, the seal bar squeezes molten polymer from the interface and produces a weak edge tear. For retort processing at 121°C, the sealant film must be laminated rather than mono-layer because the laminate adhesive and sealant interface can fail if the sealant layer softens excessively; published data for this specific configuration is limited, so converter trials are required for each film gauge.

    Standard or regulationProperty evaluatedTypical target
    ASTM F1921-23Hot-tack at 110°C, 0.5 s4.0–6.0 N/15 mm
    ASTM F88/F88M-21Seal strength after 0.5 s, 0.4 N/mm²2 N/15 mm at 95–105°C
    FDA 21 CFR 177.1520(c)Olefin polymer food contactConforms
    EU No 10/2011Overall migration<10 mg/dm²

    At packaging line temperatures below -20°C, the fracture mode of frozen food films shifts from slow yielding to dynamic crack propagation, and the molecular architecture of Exceed mLLDPE 3518PA provides a measurable advantage over butene-based LLDPE of identical density. A 40 µm blown film used for frozen vegetable pouches on a vertical form-fill-seal machine is subjected to repeated impact during filling and palletization; the low density of 0.918 g/cm³ and the hexene short-chain branching distribution allow the film to retain a high proportion of its room-temperature impact energy at freezer temperature. Converter trials on a 30 µm film report dynamic puncture values measured by ASTM D3420-14 that remain above 2 J at -25°C, whereas a conventional C4-LLDPE of density 0.920 g/cm³ drops below 1.2 J under the same conditions. The primary process limitation is not the freezer temperature but the increased stiffness of the film at low temperature, which requires a decrease in haul-off speed by 10–15% to avoid bubble flutter. For seal integrity at freezer conditions, the same heat-sealing parameters as in stand-up pouches apply, but the seal bar temperature is raised by 5°C because the cold film absorbs heat from the jaw before polymer interdiffusion begins.

    Low-gel blown film for high-speed e-commerce mailer converting

    Film for e-commerce mailers produced from Exceed mLLDPE 3518PA is specified primarily by gel count and by tear propagation resistance after flexographic printing, because the converting line subjects the web to repeated bending and surface tension changes. The metallocene catalyst system yields a lower gel density than Ziegler-Natta butene LLDPE of equivalent density, and the 0.918 g/cm³ resin is commonly run in a three-layer coextrusion with a white masterbatch in the core layer and neat 3518PA in the skin layers. On a 55 mm blown film line with 2.0 mm die gap and BUR 2.2, melt temperature is held at 195°C–205°C to avoid oxidised gel formation. A typical mailer converter specification tolerates fewer than 20 gels per 10 m² at sizes larger than 200 µm under ASTM D3351-10 gel count methodology; this is a critical threshold for mailers with high printed coverage. Elmendorf tear values in the machine direction exceed 250 g at 25 µm under ASTM D1922-09, providing resistance against tearing at perforated opening lines. The surface energy of the film must be raised to 38–40 mN/m by corona treatment before printing, but the low additive bloom of the metallocene grade delays surface energy decay. Process boundaries include the fact that melt fracture can occur at high line speeds if the die gap is reduced below 1.6 mm, and the film can lose its antistatic properties in low-humidity environments below 20% RH if the skin layer additive package is not adjusted.

    When 3518PA is compounded into post-consumer recyclate for injection-moulded crates

    The value of Exceed mLLDPE 3518PA as a toughness modifier for post-consumer recycled polyethylene depends on the melt index mismatch between the recycle fraction and the metallocene modifier. Post-consumer crates and pallets are commonly moulded from a mixed polyolefin fraction with a melt index of 0.5–1.0 g/10 min and a density of 0.93–0.94 g/cm³; direct use of this fraction produces notched impact failures and weld lines that cannot be eliminated by increasing melt temperature alone. A letdown of 10–15 wt% 3518PA into the recycle feedstock introduces controlled hexene short-chain branching and improves low-temperature tensile impact in ASTM D1822-13 testing. The improvement is not purely compositional: the dispersion of the metallocene phase requires a screw with dispersive mixing elements, and a single-stage 22:1 L/D screw with a compression ratio of 2.5:1 often leaves unmelted metallocene domains in the part. Converter data for a mixed recycled HDPE/PP stream show a 30–60% increase in tensile impact strength at 15 wt% addition, but the exact value varies with residual polypropylene content and moisture. The use of the modifier also shifts the melt flow of the compound upward by approximately 0.2–0.4 g/10 min per 10 wt% addition, which reduces peak injection pressure by 5–10%. Pre-drying is not required for the metallocene modifier, but the recyclate fraction must be dried at 75°C for 2 h when its moisture content exceeds 0.1 wt%, to prevent gas splay. The operational boundary is the contamination level: recycled fractions containing more than 2 wt% polyamide or paper fibre cause gas splay and weak weld lines that cannot be masked by the metallocene fraction.

    On cast film lines producing pallet overwrap, Exceed mLLDPE 3518PA is used as a toughness component in a three-layer A/B/A construction, not as the cling layer. The absence of long-chain branching in the metallocene resin limits neck-in on cast film lines, while the 3.5 g/10 min melt index allows high drawdown at lower melt temperatures than high-MI cast LDPE. When 3518PA is blended with a high-cling ultra-low-density ethylene-octene copolymer at 20–30 wt%, the resulting 20 µm film exhibits machine-direction tear resistance that prevents edge tear during pre-stretch. The process window for cast film is narrower than blown film; lip gap settings below 0.5 mm generate melt stress sufficient to initiate flow instabilities, and chill roll temperature below 18°C can quench the film surface too rapidly, producing excessive film curl. Stretch force retention is measured at 200% elongation; the 3518PA-containing layer increases retained force after 24 h compared with a conventional butene LLDPE blend. Published data for this specific configuration is limited, and converter trials should verify cling and unwind behaviour.

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    Certification & Compliance
    More Introduction

    ExxonMobil Exceed mLLDPE 3518PA is an ethylene-1-hexene copolymer produced on a metallocene catalyst platform. The grade is defined for blown-film extrusion by a nominal melt index of 3.5 g/10 min at 190 °C under 2.16 kg load per ASTM D1238-20 and a nominal density of 0.918 g/cm³ per ASTM D1505-18. The melting peak determined by differential scanning calorimetry is typically near 119 °C per ASTM D3418-21. The alphabetic suffix designates the specific product variant within the 3518 series; the base polymer architecture remains an mLLDPE with controlled short-chain branching, while the suffix reflects the additive formulation or stabilization package rather than a change in density or melt-flow class.

    PropertyTypical ValueTest Method
    Melt index3.5 g/10 minASTM D1238-20, 190 °C/2.16 kg
    Density0.918 g/cm³ASTM D1505-18; equivalent ISO 1183-1:2019
    Melting peak119 °CASTM D3418-21; equivalent ISO 11357-3:2018

    The base resin is supplied in pellet form and is intended primarily for monolayer and coextruded blown-film applications. It is not recommended for rotomolding, blow molding of bottles, or high-shear injection molding because the narrow molecular weight distribution and melt-flow class do not provide the melt strength or packing behavior required by those processes. The material is not hygroscopic, and predrying is generally unnecessary under controlled warehouse storage. However, surface condensation on cold pellets transferred into a warm production area can generate film defects when relative humidity exceeds 60%; in that circumstance, hopper drying at 60 °C to 70 °C is used to remove surface moisture only.

    How Does Uniform Short-Chain Branching Influence Tear, Impact, and Seal Response Compared With Ziegler-Natta LLDPE?

    The principal difference between ExxonMobil Exceed mLLDPE 3518PA and conventional Ziegler-Natta ethylene-hexene or ethylene-butene LLDPE lies in the distribution of comonomer across the molar mass distribution. In conventional Ziegler-Natta LLDPE, comonomer incorporation is often highest in the low-molecular-weight fraction, producing a compositionally heterogeneous resin with a pronounced population of highly crystalline, low-comonomer chains. In the metallocene-catalyzed architecture of 3518PA, 1-hexene comonomer is incorporated more uniformly, and the resulting composition distribution is narrower. That molecular arrangement reduces the fraction of thick lamellae and increases the tie-chain concentration in blown film, which is directly relevant to toughness response.

    At equivalent density and melt index, films produced from 3518PA generally show higher dart impact values per ASTM D1709 and higher Elmendorf tear values per ASTM D1922 than a Ziegler-Natta LLDPE of the same nominal density and melt index. The 1-hexene comonomer contributes longer branches than butene and is associated with improved tear resistance at comparable density because the longer branch segments create more effective interlamellar tie loops. Optical response is also affected: the more homogeneous crystalline morphology reduces light-scattering domains, yielding lower haze per ASTM D1003 and higher gloss per ASTM D2457 in many monolayer films compared with conventional heterogeneous LLDPE. Published film property values for 25 µm monolayer film are equipment-dependent; typical tensile yield values fall in the range of 10–11 MPa in both machine and transverse directions per ASTM D882, with Elmendorf tear values commonly reported in the 250–400 g range. These values are not specification limits and vary with die gap, blow-up ratio, frost-line height, and cooling rate.

    The same narrow composition distribution also lowers the high-molecular-weight tail that contributes to melt elasticity. As a result, the neat resin exhibits lower bubble stability than autoclave LDPE or broad-molecular-weight LLDPE under identical die conditions. The reduced melt elasticity can be advantageous for drawdown and gauge uniformity but requires greater attention to air-ring control, die geometry, and frost-line management. The lower melting peak near 119 °C permits earlier seal initiation than higher-density or higher-melting LLDPE grades; seal strength should be measured per ASTM F88 because sealing response is governed by film gauge, dwell time, sealing pressure, and temperature plateau.

    On single-screw grooved-feed blown-film extruders with 25:1 to 30:1 L/D, the resin is typically processed at barrel set points from 180 °C to 220 °C and melt temperatures from 190 °C to 230 °C. Die gaps from 1.5 mm to 2.5 mm and blow-up ratios from 2.0:1 to 3.0:1 are common. Because of the low melt elasticity, die-lip melt fracture and bubble oscillation can develop at high shear rates or excessive frost-line heights. Reducing die gap to 1.2 mm can increase back pressure but may improve gauge control in some die configurations. Sustained melt temperatures above 260 °C should be avoided to reduce the risk of polymer degradation and gel formation. The recommended purging procedure is to use a polyethylene purging compound or a transition through a commercial LLDPE purge grade before shutdown.

    When 3518PA Replaces LDPE-Rich Blends in Blown Film

    Replacement of an LDPE-rich blown-film formulation with 3518PA shifts the property balance because autoclave LDPE provides high melt strength from long-chain branching, whereas metallocene LLDPE provides higher solid-state toughness and better optical homogeneity from its narrower composition distribution. In practice, the neat resin can be converted on standard LLDPE blown-film lines, but bubble stability is lower than that of an LDPE-rich blend. Many converters add 10–30 wt% LDPE to 3518PA to restore bubble stability at blow-up ratios above 2.5:1. That addition reduces the dart impact and tear benefits of the mLLDPE phase and increases haze in a measurable manner, although the exact shift depends on the LDPE melt index and long-chain branching level. Published data for this specific blend configuration are limited; the response is commonly evaluated in plant trials rather than predicted from neat resin datasheets.

    At LDPE addition levels above 30 wt%, the toughness advantage of the metallocene resin is progressively reduced, and the blend begins to approach the bubble stability and optical profile of conventional LDPE-rich films. The substitution of 3518PA for LDPE-rich blends is therefore most effective where film toughness, downgauging, and seal performance have higher value than maximum bubble stability. In coextruded structures, 3518PA is used in core or skin layers to contribute puncture resistance, tear resistance, and low-temperature seal response while the outer or machine-side layers may contain LDPE or HDPE for process stability and stiffness.

    Commercial usage is concentrated in heavy-duty shipping sacks, industrial liners, agricultural silage film, collation shrink, and bulk container liners. In these applications, the resin is processed at typical film gauges from 25 µm to 150 µm, either neat or in let-down blends. The product is also used in form-fill-seal structures where seal initiation, hot-tack, and abuse resistance are specified per ASTM F88 and ASTM F1921, respectively. On high-speed bag conversion lines, the additive package of the suffix variant should be matched to the required coefficient of friction and blocking behavior; if the base additive loading is insufficient for a particular sealing jaw design or film path, additional slip or antiblock masterbatch may be introduced at the hopper. That adjustment should be evaluated for haze and seal-strength loss because external additives can alter surface energy and sealing response.

    The product is generally not combined with polar additives or highly acidic processing aids unless compatibility has been demonstrated; unexpected additive interactions can shift surface friction, affect thermal stability, or generate plate-out on the die lip. For food-contact applications, the final film must meet extraction and migration limits under the intended condition of use, not merely the resin supplier’s regulatory status.

    Regulatory Status and Analytical Test Matrix

    Exceed mLLDPE 3518PA is an olefin polymer. In the United States, food-contact use is typically evaluated under FDA 21 CFR 177.1520, subject to the olefin polymer identity, density, and extraction limitations of the final article. In the European Union, the relevant frame is Commission Regulation (EU) No 10/2011, including the overall migration limit of 10 mg/dm² and applicable specific migration limits for additives and monomers. The supplier safety data sheet should be consulted for current REACH registration status under Regulation (EC) No 1907/2006 and for any Substances of Very High Concern declarations. RoHS Directive 2011/65/EU restrictions apply to electrical and electronic equipment and not to the polymer as a bulk material; compliance of the finished film or component must be assessed at the article level.

    Regulatory or Standards FrameRelevant DesignationEnd-Use Condition
    US food contactFDA 21 CFR 177.1520Final article must comply with olefin polymer identity and extraction limits for the intended food type and temperature
    EU food contactCommission Regulation (EU) No 10/2011Overall migration limit 10 mg/dm²; specific migration limits apply to authorized additives
    Chemical regulationREACH Regulation (EC) No 1907/2006SVHC and authorization status to be confirmed from the supplier safety data sheet
    Restricted substances in electrical equipmentRoHS Directive 2011/65/EUApplies to finished electrical or electronic articles; bulk polymer status does not exempt final-article requirements

    For converters qualifying the resin for food contact, migration testing under actual film thickness, food simulant, time, and temperature is required. The supplier’s product documentation provides typical properties, but the final article specification must be developed from measurements on the converter’s own film line because gauge uniformity, cooling rate, and additive masterbatch loadings materially affect extractive and organoleptic performance.

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