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Dow ELITE mLLDPE 5110G

    • Product Name: Dow ELITE mLLDPE 5110G
    • 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 374992
    Product Name Dow ELITE mLLDPE 5110G
    Polymer Type Metallocene Linear Low Density Polyethylene (mLLDPE)
    Comonomer 1-Octene
    Physical Form Pellets
    Color Natural

    As an accredited Dow ELITE mLLDPE 5110G factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Dow ELITE mLLDPE 5110G is packaged in 25 kg bags, 40 bags per 1,000 kg pallet.
    Container Loading (20′ FCL) 20′ FCL: Dow ELITE mLLDPE 5110G polyethylene resin in 25 kg bags, palletized, stretch-wrapped, and secured for export shipment.
    Shipping Dow ELITE mLLDPE 5110G is a non-hazardous polyethylene resin shipped as pellets in sealed bags or octabins. It is not regulated for transport by DOT, IATA, IMDG, or ADR. Keep dry, protected from heat and contamination, and handle with standard lifting equipment. Store in a cool, dry, ventilated area.
    Storage Store Dow ELITE mLLDPE 5110G in a cool, dry, well-ventilated warehouse, away from direct sunlight, heat, ignition sources, moisture, and incompatible chemicals. Keep original packaging closed, palletized, and protected from dust, UV exposure, and physical damage. Avoid temperature extremes, maintain good housekeeping and drain protection, follow the SDS and local regulations, and use first-in/first-out stock rotation.
    Shelf Life Typically two years from manufacture when stored unopened in original packaging under dry, ambient conditions, away from direct sunlight.
    Application of Dow ELITE mLLDPE 5110G

    In vertical form-fill-seal (VFFS) conversion of dry food, instant powders, and ground coffee, Dow ELITE mLLDPE 5110G is processed as an mLLDPE-rich blown film layer. The resin is specified at a nominal density of 0.919 g/cm³ per ASTM D1505-18 and a melt flow rate of 1.0 g/10 min per ASTM D1238-20 at 190 °C/2.16 kg. On production-scale monolayer and three-layer blown film equipment with barrier-screw extruders of 30:1 L/D, die gaps from 1.8 mm to 2.2 mm, and dual-lip air rings, converters commonly blend 70–80 wt% 5110G with 20–30 wt% high-pressure LDPE having a melt flow rate below 0.5 g/10 min. The LDPE component raises low-shear melt strength and stabilizes the bubble at blow-up ratios between 2.5:1 and 3.0:1. Failure modes observed on VFFS lines include intermittent seal contamination from cocoa dust, sugar fines, or salt aerosol, where conventional Ziegler-Natta LLDPE sealant layers can require manual line-speed derating to maintain package integrity; the mLLDPE-rich sealant layer reduces this occurrence, but line-specific trials are required. Seal initiation temperature is typically 5–12 °C lower than that of a comparable 0.918 g/cm³ Ziegler-Natta LLDPE under the same heat-seal gradient procedure, although published data for this specific configuration is limited and must be confirmed on the target production line. Heat-seal conditions on rotary seal jaws are commonly set with dwell times of 80–120 ms and jaw face temperatures of 115–140 °C; the lower end of this range becomes accessible when 5110G content exceeds 70 wt%. Hot-tack performance is evaluated according to ASTM F1921-18, while ultimate seal strength is measured per ASTM F88-21 after 24 h conditioning at 23 °C/50% RH. For indirect food contact, the resin must be used within blends that meet FDA 21 CFR 177.1520(c) 3.1a or 3.2a and the overall migration limit of 10 mg/dm² under EU Regulation 10/2011. Insufficient hot-tack at the filling line is not corrected by raising jaw temperature alone; seal pressure and dwell time interact with package film gauge, and seal-bar temperatures above 180 °C can delaminate coextruded tie layers if present.

    What Limits Layer Uniformity in Three-Layer Heavy-Duty Sack Coextrusion?

    High-output heavy-duty sack lines typically place 5110G in the core or sub-skin layer to increase puncture resistance and machine-direction tear propagation resistance. The critical processing constraint is not melt temperature but melt-flow distribution across the spiral mandrel. In a three-layer coextrusion configuration with a 400 mm die, 30:1 L/D core extruder, and two 25:1 L/D skin extruders, core-layer 5110G fraction between 30 wt% and 40 wt% is common when skin layers are HDPE with density near 0.952 g/cm³. The interlayer viscosity mismatch is lower than with conventional LLDPE because 5110G has a controlled short-chain branching distribution and a shear-thinning index that lies between LDPE and broad-MWD HDPE. Dart impact values are measured by ASTM D1709-16a Method A for films up to 50 μm; for sacks at 80–120 μm total gauge, Method B is commonly used. Elmendorf tear resistance is evaluated per ASTM D1922-15 in both MD and TD after conditioning at 23 °C and 50% RH. Processors report that melt pressure fluctuations above 5% on the core extruder can shift the core-layer thickness by ±2 μm across the web, producing low-spot dart impact failures during filled-drop testing. To prevent this, screw speeds are trimmed so that the core extruder operates between 70% and 85% of maximum torque, and die temperature is maintained within ±3 °C of setpoint. Blending 10–20 wt% LDPE into the core layer raises bubble stability on high-stalk lines and reduces edge tear during gusseting. The as-supplied resin should be verified for slip and antiblock content; many heavy-duty sack formulations are built on additive-free 5110G and require separate masterbatch addition if sacks need a coefficient of friction below 0.35, tested per ISO 8295:2018. Film blocking and additive migration must be revalidated because migratory slip agents can reduce long-term lamination bond strength if sacks are subsequently printed or laminated.

    Because adhesive-laminated stand-up pouches require a sealant web that maintains hot-tack over gusset folds, converters specify 5110G in the sealant-web position of structures where the outer web may be 12 μm polyester, 18–20 μm biaxially oriented polypropylene, or 7–9 μm aluminium foil. Blown film made from 5110G at 40–60 μm thickness is corona-treated to a wetting tension of 38–42 mN/m per ASTM D2578, then laminated using solventless polyurethane adhesives at coat weights from 2.0 g/m² to 3.5 g/m². The sealant layer contributes caulkability over gusset folds and heat-seal through residual product contamination. In rotary fill-seal machines running liquid pastes or stock cubes, the sealant layer is required to maintain hot-tack above 2.5 N/25 mm during the return stroke of the seal jaw, tested per ASTM F1921-18 at sealing temperatures between 110 °C and 130 °C. The heat-seal strength of the laminated structure is measured per ASTM F88-21 using 25 mm wide strips cut perpendicular to the seal. A conversion specification commonly requires seal strength to exceed 1,500 g/25 mm at seal initiation and remain above 900 g/25 mm after exposure to 5 wt% sodium chloride slurry at 40 °C for 72 h, although published data for this specific resin configuration is limited and must be generated on the actual laminate. For food contact in the European Union, the sealant film must meet overall migration below 10 mg/dm² under EU Regulation 10/2011, with testing in food simulant A, B, or D2 depending on the packaged product. Under US FDA, the resin may be used as an olefin polymer in compliance with 21 CFR 177.1520(c) 3.1a or 3.2a when the finished film meets the extractables limitations applicable to the intended food type. In retort or hot-fill conditions above 100 °C, the sealant film approaches its practical temperature limit, and the pouch must be downgauged only after burst testing per ASTM F2054 confirms no seal creep.

    Table 1. Compliance and characterization matrix for 5110G in flexible packaging
    ApplicationRegulatory or mechanical obligationStandard or methodTypical control point
    Food-contact VFFS filmsOlefin polymer compliance21 CFR 177.1520(c)End-use extraction per food type
    Pouch sealant webOverall migration in EUEU 10/201110 mg/dm²
    Heavy-duty sackImpact and tear resistanceASTM D1709-16a, ASTM D1922-15Film gauge-dependent
    Frozen-food packagingLow-temperature impactASTM D1709-16a at -20 °CNo brittle failure
    Bag-in-box linersFlex-crack resistanceASTM F392-22Depends on barrier structure

    When Seal Through Frost Becomes the Controlling Variable in Frozen-Food Lines

    Vertical and horizontal form-fill-seal machines used for individually quick-frozen vegetables, seafood portions, and frozen fruit packs place the sealant layer in contact with water frost and product fines at surface temperatures between -25 °C and -10 °C. Under these conditions, seal-bar dwell is often limited to 40–80 ms because excessive heat transfer can melt product surface and create destructive steam pressure at the seal interface. Films containing 5110G as the sealant layer exhibit hot-tack behaviour that allows the jaw to open under a short thermal budget, reducing the frequency of seal voids at package corners. The frozen-film body must also resist brittle puncture when frozen packages contact sharp edges of ice crystals or machine guides. Low-temperature impact resistance is evaluated using ASTM D1709-16a after conditioning film samples at -20 °C for 48 h, while slow puncture resistance is measured using ASTM D5748-19 or ISO 7765-1:2019. Processors specifying 5110G in a 70 wt% blend with LDPE report fewer film splits during high-speed bagging, but published data for this specific manufactured configuration remains limited because freezer-line performance is strongly influenced by bag geometry and fill temperature. The recommended film gauge for IQF vegetable bags is normally 50–70 μm, with the inner sealant layer comprising at least 15 μm of the total structure. Corona treatment should be limited to the print surface only; re-treating the sealant side above 36 mN/m can reduce heat-seal strength by oxidizing surface olefin chains, measured as a drop in ASTM F88-21 peel force. Anti-fog masterbatches are introduced at 1–2 wt% only after compatibility testing, because glycerol-ester or sorbitan-ester additives can migrate to the surface and either increase or suppress hot-tack depending on concentration.

    Agricultural Silage Film Blending and UV Stabilizer Loading

    For silage conservation films and greenhouse cladding films, 5110G is incorporated into three-layer blown film structures to increase puncture toughness without reducing flexibility at low installation temperatures. Typical total gauge for silage film is 25–80 μm, while greenhouse cladding may reach 100–180 μm. The resin is blended with LDPE at 20–30 wt% to provide bubble stability on high-stalk lines and to improve fold retention during bale wrapping. Formulations include hindered-amine light stabilizer and UV absorber masterbatches at total additive loadings of 2–4 wt%, with dosage adjusted by geographic UV index and film thickness. The dispersed additives are not chemically bound; their migration to the film surface and loss during weathering are monitored using ISO 4892-2:2013 accelerated UV exposure and subsequent tensile testing per ASTM D882-18. Film puncture resistance before and after weathering is measured using ISO 7765-1:2019 or ASTM D5748-19. In silage bale wrap, the film must survive direct contact with corn stalks and grass stems under tension from a round baler. Processors report that a reduction from 30 μm to 25 μm is considered only when the 5110G content in the core layer exceeds 50 wt%; below that threshold, field puncture rates become excessive in dry hay containing lignified stems. Bubble stability is managed by maintaining the frost line height below 8 die diameters and die tip temperatures at 210–220 °C. The resulting film is sealed during bale wrapping through self-adhesion; the peel force between overlapping layers is not standardized, but practical field adhesion is checked by a 180° peel test on wrapped cores at 23 °C. The resin itself does not contain UV stabilizers; agricultural film producers must validate the dispersion of the purchased masterbatch by measuring film haze per ASTM D1003-21 and yellowness index per ASTM E313-20.

    In bag-in-box liquid packaging for wine, dairy liquids, and post-mix syrups, 5110G is specified in the inner contact layer of coextruded films used to fabricate flexible liners with volume capacities from 2 L to 1,000 L. The primary mechanical failure mode in filling and transport is flex-crack pinholing, which is evaluated using ASTM F392-22 at 4 °C and 40 °C after 2,000 flex cycles. Compared with conventional LLDPE liners of the same gauge, structures containing 5110G show lower pinhole density after flex testing, but the exact improvement depends on the adjacent EVOH or polyamide barrier layer and the tie resin used. Coextrusion is typically performed on a three-layer or five-layer blown film line with total gauge between 60 μm and 100 μm, where 5110G forms the food-contact skin layer at 15–20% of total thickness. Melt filtration with 250 μm/180 μm screen packs is specified to reduce undispersed gel structures in the contact layer; published gel count data for 5110G is limited, so inline filtration is treated as a precaution rather than a correction for a measured defect. The inner layer must also survive sealing against polyethylene fitments at 200–220 °C without thinning below 5 μm at the flange edge. Seal strength around fitments is tested per ASTM F88-21 using ring specimens cut around the fitment base. For wine and dairy products, migration testing follows EU Regulation 10/2011 with simulant D2 for high-fat dairy or simulant A for aqueous wine, and the overall migration limit is 10 mg/dm². Under US FDA, compliance is established under 21 CFR 177.1520(c) for olefin polymers, and the finished liner must not impart organoleptic taint above the sensory threshold specified by the buyer. The resin must not be blended with slip or antistatic additives unless their migration is acceptable for the specific liquid type, because low-molecular-weight additives can appear in headspace gas-chromatography screening at sub-ppm levels.

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    Certification & Compliance
    More Introduction

    Dow ELITE 5110G is an enhanced linear low density polyethylene produced through a single-site INSITE catalyst platform. Neat resin density is reported as 0.9255 g/cm³ when tested under ASTM D792, and melt index is reported as 0.85 g/10 min when tested under ASTM D1238 at 190 °C/2.16 kg. These values place the grade in the mid-density LLDPE range used for blown film. The chemical structure is not that of a conventional Ziegler-Natta LLDPE; the single-site catalyst introduces short-chain branches along the polymer backbone with a more uniform distribution, and a low concentration of long-chain branching is used to modify shear thinning. This combination is intended for films requiring puncture resistance, seal performance, and the ability to downgauge from conventional LLDPE constructions.

    The values in Table 1 are typical neat resin values; they do not replace the product specification or the certificate of analysis. Film property values for this grade are not fixed because dart impact, tear, and seal strength depend on die gap, blow-up ratio, film thickness, chill-air temperature, and orientation. Comparative statements between 5110G and other polyethylenes should therefore be evaluated on the same blown film line.

    PropertyTest MethodTypical Neat Resin Value
    DensityASTM D7920.9255 g/cm³
    Melt indexASTM D1238, 190 °C/2.16 kg0.85 g/10 min
    DSC peak melting temperatureASTM D3418122 °C approximate, thermal-history dependent

    What Distinguishes Single-Site 5110G from a Conventional Ziegler-Natta LLDPE?

    The principal difference is not the density or the melt index but the distribution of comonomer along the chain. In a conventional Ziegler-Natta LLDPE, comonomer incorporation is highest in the low-molecular-weight fraction, creating a broad composition distribution, a wider melting endotherm, and a larger amount of low-temperature amorphous material. In 5110G, the single-site catalyst maintains a more regular comonomer placement. The practical result is a lower seal initiation temperature than a conventional LLDPE of equal density because the crystalline lamellae melt over a narrower interval. This difference is evaluated in the laboratory by hot-tack tests under ASTM F1921 and heat seal strength tests under ASTM F88/F88M; published comparative data for metallocene LLDPE generally show hot-tack and seal strength advantages over Ziegler-Natta LLDPE at equivalent film thickness.

    The narrower molecular weight distribution also reduces the low-molecular-weight species available to migrate or form extractable material. Extraction testing under FDA 21 CFR 177.1520(c) or EU Regulation (EU) No 10/2011 must be performed on the final film, but single-site resins are typically selected when the final article must meet low extractable limits. The melt elasticity and bubble stability are affected by long-chain branching; although the long-chain branching level is low, it is sufficient to provide shear thinning and melt tension. Published data for the exact long-chain branching index of 5110G is limited, and bubble stability should be optimised on the target extrusion line rather than inferred from another polyethylene grade.

    Compared with high-pressure LDPE, 5110G generally exhibits higher tensile strength and puncture resistance at equal thickness, but lower melt strength and less strain hardening. In blown film lines accustomed to LDPE, screw torque may be higher because the resin does not shear thin to the same extent. The difference in extensional viscosity is measurable as a lower maximum take-off speed before bubble instability; a production line with internal bubble cooling may offset this behaviour. Compared with a high-flow metallocene LLDPE of melt index 1.0 g/10 min or higher, 5110G is selected when toughness and downgauging are more important than high-speed thin-gauge output.

    In plant-scale evaluation on a 55 mm single-screw grooved-feed extruder with a 24:1 L/D barrier screw and a 120 mm spiral mandrel die, the resin is typically processed with a die gap of 2.0–2.5 mm, a blow-up ratio of 2.2:1 to 3.0:1, and a melt temperature of 200–230 °C. The actual set-point within this range is adjusted to eliminate melt fracture at high output and to control the frost-line height. At equivalent die gap and output, the metering pressure of 5110G may be higher than that of a high-pressure LDPE with a similar melt index because the linear backbone and narrower molecular weight distribution produce lower shear thinning. If the die pressure exceeds the limit of the extruder drive, the die gap can be widened within the upper boundary; however, excessive die gap will reduce orientation and may lower dart impact resistance.

    Bubble stability is more sensitive to air-ring velocity and internal bubble cooling than for a conventional high-pressure LDPE. A dual-lip air ring with internal bubble cooling is typically required when the film is processed at thicknesses below 50 µm at high output. The frost-line height is usually set between 2 and 3 die diameters; a shorter frost-line height may increase blocking and raise the coefficient of friction, while a taller frost-line height may reduce impact strength through excessive orientation. Pre-drying is not required for the neat resin because polyethylene is not hygroscopic; however, condensation on pellets stored in an uncontrolled outdoor silo can introduce surface moisture and generate steam splay in the film.

    Die Gap, Blow-Up Ratio, and Melt Temperature Requirements on a Single-Screw Blown Film Line

    When the resin is used in a high-stalk bubble configuration, the stalk height and the melt strength of 5110G interact to influence neck stability. A high-stalk configuration is often selected to improve mechanical properties in the machine direction; in this configuration the die gap is kept at the lower end of the recommended range to increase shear orientation. Melt temperature at the die is maintained at 216–232 °C in some production lines to reduce gel formation; however, exceeding 250 °C during short hold-up time is not advisable because oxidative degradation may generate carbonised material that appears as black specks. The use of a screen pack with mesh sizes 20/40/60 or 20/40/80 is common to protect the die from adventitious contamination; differential pressure across the screen pack should be monitored and recorded at start-up to identify premature fouling.

    The grade may be blended with LLDPE or LDPE to adjust melt strength and stiffness. When LDPE is added at 10–30 wt%, bubble stability improves, but the dart impact and tear strength move toward those of the LDPE phase. The exact blend ratio is not a fixed rule; it is determined by the required balance between seal performance and bubble control on the specific line. Incompatibility with process lubricants is not generally reported for polyethylene, but halogenated flame retardants and some amine-based stabilisers can contribute to surface deposit or die-lip build-up if they decompose at processing temperatures. The shear viscosity curve of 5110G differs from that of a broad-MWD LLDPE even when the melt index is identical; therefore, extruder barrel temperature profiles and back-pressure settings from a previous LLDPE grade cannot be transferred without evaluation.

    Heavy-duty shipping sacks manufactured from 80–150 µm blown film often require puncture resistance under ASTM D5748 and dart impact under ASTM D1709 Method A. The downgauging potential of 5110G compared with a conventional LLDPE of equal density arises from the more uniform comonomer incorporation, which reduces the number of local amorphous regions that initiate crack propagation. In practice, a converter may reduce film gauge by 10–20% only after line validation; published data for this specific configuration is limited, and the actual gauge reduction depends on the sealant layer, print layer, and gusseting geometry. The resin is also used in industrial liners and collation shrink film, where the seal integrity under filled-load transport is tested by drop tests and by tensile seal strength under ASTM F88/F88M.

    When Film Seal Initiation and Extractable Restrictions Exceed Standard LLDPE Limits

    In flexible packaging structures that require low-temperature seal initiation below 105 °C, 5110G is often positioned against conventional LLDPE sealants. The benefit is not solely the melt index or density; it is the narrow melting range. Laboratory heat seal tests under ASTM F2029 are used to determine the seal initiation temperature on the target gauge, using a dwell time of 0.5 s and pressure of 0.275 MPa. The reported seal initiation value varies from line to line because the film surface temperature at the seal bar is influenced by heat transfer through the film and by the backing material. The requirement for low extractable material is evaluated under 21 CFR 177.1520(c) for food-contact articles, and the final compliance statement must include the entire film structure rather than the neat resin.

    RequirementStandard or RegulationEvaluation Basis
    Food contact extractionFDA 21 CFR 177.1520(c)Final film, hexane extractable limits, end-use conditions
    European food contactEU Regulation (EU) No 10/2011Overall migration, specific migration, final formulation
    REACH registrationEC 1907/2006SDS and registration status, substance verification
    RoHS screeningIEC 62321Not normally a constraint for neat polyolefin; additive package may require verification

    Because the exact lot-to-lot melt index and density are controlled within manufacturer specifications, the extrusion calibration should be rechecked after each polymer lot change. The extruder barrel temperature profile, screw speed, and back-pressure settings from a previous LLDPE grade cannot be transferred to 5110G without evaluation because the shear viscosity curve differs from a broad-MWD LLDPE even when the melt index is identical. The resin is supplied in pellet form, and the recommendations for silo storage are similar to other polyolefins: avoid direct sunlight, keep bulk temperature below 50 °C, and purge with dry air when condensation is possible. No additional drying is needed under normal handling conditions.

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