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ExxonMobil Exceed LLDPE 1018MA

    • Product Name: ExxonMobil Exceed LLDPE 1018MA
    • 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 269311
    Density 0.918 g/cm³ (ASTM D1505)
    Melt Flow Rate 1.0 g/10 min (190°C/2.16 kg, ASTM D1238)
    Melting Point 120°C (DSC)
    Crystallization Point 100°C (DSC)
    Vicat Softening Point 105°C (ASTM D1525)
    Tensile Strength At Yield 13 MPa (film, MD/TD, ASTM D882)
    Tensile Strength At Break 44 MPa MD / 39 MPa TD (film, ASTM D882)
    Elongation At Break 470% MD / 620% TD (film, ASTM D882)
    1 Secant Modulus 180 MPa MD / 210 MPa TD (film, ASTM D882)
    Dart Drop Impact F50 600 g (film, ASTM D1709)
    Haze 10% (film, ASTM D1003)
    Gloss At 60 60 GU (film, ASTM D2457)

    As an accredited ExxonMobil Exceed LLDPE 1018MA factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing ExxonMobil Exceed LLDPE 1018MA is supplied in 25 kg polyethylene bags, palletized and stretch-wrapped for safe handling and transport.
    Container Loading (20′ FCL) 20′ FCL container loading of ExxonMobil Exceed LLDPE 1018MA: bags on pallets, securely braced and wrapped for safe transit.
    Shipping ExxonMobil Exceed LLDPE 1018MA is a linear low-density polyethylene resin supplied as free-flowing pellets. Ship in clean, dry bulk hopper trucks, railcars, or lined Gaylord boxes. Protect from moisture, direct sunlight, and contamination, storing in a cool, ventilated area until processing.
    Storage Store ExxonMobil Exceed LLDPE 1018MA in a dry, clean, well-ventilated warehouse, away from direct sunlight, heat, and ignition sources. Keep containers sealed to prevent moisture and contamination. Avoid outdoor exposure and excessive stacking pressure. No special temperature control is required, but ambient conditions below 50°C are recommended.
    Shelf Life Shelf life is indefinite when stored in a dry, clean area away from direct sunlight and extreme heat.
    Application of ExxonMobil Exceed LLDPE 1018MA

    At a nominal density of 0.918 g/cm³ and melt flow index of 1.0 g/10 min measured under ISO 1133-1:2022, ExxonMobil Exceed 1018MA is extruded as monolayer blown film for dry-food liners and frozen-food pouches on single-screw lines with 25:1–30:1 L/D ratios. A 65 mm grooved-feed extruder feeding a 250 mm spiral mandrel die with 1.8–2.3 mm die gap maintains melt pressure below 450 bar at 100–120 kg/h output when zone temperatures are held at 165 °C, 185 °C, 200 °C, 205 °C, and die temperature at 210 °C. The stalk is cooled with a frost line height of 6–9 die diameters at blow-up ratio 2.2:1–2.8:1; above 3.0:1, machine-direction tear resistance measured under ASTM D1922 increases at the expense of transverse-direction impact, which is governed by ASTM D1709 Method A on 25 µm film. In this thickness range, published datasheet values for 1018MA indicate dart drop values above 800 g, tensile elongation at break above 500 % under ASTM D882, and haze below 8 % under ASTM D1003. The material does not require pre-drying at ambient relative humidity below 60 %; however, condensation on granules stored outdoors below 10 °C warrants a 60 °C hopper dryer for 2 h to prevent surface splay. Melt fracture in the die lip region is managed with fluorine-free polymer processing aid at 300–500 ppm rather than increasing die gap above 2.3 mm, which degrades bubble cooling uniformity. Compliance for food contact is governed by the olefin polymer provisions of FDA 21 CFR 177.1520(c) and overall migration limits of 10 mg/dm² in EU Regulation (EU) No 10/2011, Annex I. The resin is processed neat or with 10 ± 3 wt% low-density polyethylene to improve bubble stability at film gauges below 30 µm; higher LDPE fractions raise the seal initiation temperature by 3–5 °C under ASTM F88, which is undesirable for high-speed horizontal form-fill-seal packaging of oxygen-sensitive dry foods.

    Process variableSet point / observed rangeReference instrument or standard
    Barrel zone 1160–170 °C65 mm grooved-feed extruder, 30:1 L/D
    Barrel zone 2180–190 °C65 mm grooved-feed extruder, 30:1 L/D
    Barrel zone 3195–205 °C65 mm grooved-feed extruder, 30:1 L/D
    Adapter / die205–210 °C250 mm spiral mandrel die
    Die gap1.8–2.3 mmFeeler gauge, cold die lip
    Blow-up ratio2.2:1–2.8:1Optical bubble diameter measurement
    Frost line height6–9 die diametersInfrared pyrometer

    What Melt Pressure Instability Occurs When 1018MA Is Coextruded as a 12 µm Sealant Web over HDPE?

    The coextrusion line referenced here is a three-layer blown-film configuration with 400 mm spiral mandrel die, 1.8 mm die gap, and 2.0:1 blow-up ratio, producing a 62 µm heavy-duty shipping sack structure in which 1018MA serves as the 12 µm sealant web over a 36 µm recycled LLDPE/LDPE core and a 14 µm outer high-density polyethylene skin. The sealant layer is fed at 2.5–3.0 rpm on a separate 35 mm single-screw extruder with 24:1 L/D because a 12 µm layer cools below the interfacial fusion threshold when die exit temperatures differ by more than 8 °C between adjacent layers. Melt temperature in the 1018MA extruder is limited to 204–210 °C; at 215 °C, die lip deposit from low-level oxidized gel forms within 4 h on production lines, a failure mode observed on 25 kg chemical sack lines. The substrate HDPE layer is extruded at 200–205 °C to control viscosity mismatch; a viscosity ratio above 2.0:1 between the HDPE and 1018MA melt at 210 °C destabilizes the bubble and causes gauge bands rather than interface adhesion loss. Seal strength on the 12 µm web measured after 24 h conditioning under ASTM F88 exceeds 4 N/15 mm when the seal bar is set to 115 °C and dwell 0.5 s; this value drops below 2 N/15 mm if the recycled core introduces more than 15 wt% polypropylene contamination from mixed-rigid streams. Puncture resistance of the finished sack is assessed by ASTM D5748; the specification for 25 kg inorganic powder fill is a minimum 8 N at 23 °C. Compliance for industrial packaging requires absence of lead, cadmium, mercury, and hexavalent chromium above 100 ppm total under 94/62/EC as amended and the US CONEG model legislation. The final product is used as valve sacks for precipitated silica, carbon black, and coumarone-indene resin, as well as external courier mailers where a 12 µm 1018MA seal layer permits burst-resistant sealing without contaminating the recycled stream.

    Extrusion Lamination of Kraft and Aluminium Foil with a Low-Density Metallocene Skin

    When 1018MA is melt-extruded through a 1,600 mm T-die onto 12 µm aluminium foil at 305–315 °C, the low melt flow index of 1.0 g/10 min reduces neck-in to 10–15 mm per edge at a 250 mm air gap, allowing a 12 g/m² coating weight without edge bead build-up on high-speed laminators. The extruder is a 120 mm single-screw unit with 28:1 L/D and water-cooled feed throat; screw speed is held between 60 and 80 rpm to maintain melt pressure below 300 bar at 310 °C. A fluorine-free polymer processing aid at 300 ppm is added to suppress die-lip drool, while an antioxidant package containing 0.1 wt% phosphite and 0.05 wt% phenolic stabilizer extends residence time before gel formation to 6 min at 315 °C. Temperatures above 320 °C cause oxidation of the metallocene short-chain branching and localized crosslinking, producing visible gel counts above 5 particles/m² when measured by a camera-based gel counter on the finished laminate. Adhesion to aluminium foil is controlled by the oxidation of the melt surface; if the air gap is shortened below 150 mm, adhesion measured by ASTM D1876 falls below 2.5 N/15 mm because insufficient surface oxidation occurs before the nip. A 12 µm layer of 1018MA is also used over 35 g/m² kraft paper for sack lamination, where 14 g/m² coating is applied at 310 °C and chilled on a 15 °C roller at 40 N/cm nip pressure. Compliance for beverage carton lamination is evaluated under FDA 21 CFR 177.1520(c) for the polyethylene layer and 21 CFR 177.1395 for the adhesive laminate structure when the foil and paper compose the functional barrier. The terminal products are aseptic drink carton side seams, single-serve coffee sachets, and polyester-polyethylene aluminium retort lidding with a 9 g/m² counter-laminate.

    Cast film processability of 1018MA at 1.0 g/10 min melt flow index is constrained on high-speed surface protection film lines by the resin’s narrow molecular weight distribution, which raises melt extension viscosity and limits drawdown below 20 µm unless melt temperature is increased to 235 °C. A 90 mm single-screw extruder with 30:1 L/D feeds a 1,800 mm flat die at 150 m/min line speed; the air gap is set at 10–12 cm and the polished chill roll is maintained at 18 °C to lock in low-crystallinity surface clarity. The film is compounded with 2,000–3,000 ppm synthetic silica antiblock and 500–800 ppm erucamide slip incorporated as a 3 wt% masterbatch; erucamide migration to the surface follows a 24–48 h maturation period under ASTM D6042 storage conditions, during which corona treatment levels drop by 4–6 mN/m from an initial 38–40 mN/m surface energy if the film is treated before aging. For stainless steel sheet masking, a 40 µm cast film of 1018MA is laminated to a waterborne acrylic adhesive with surface energy above 36 mN/m; direct offline corona at 3 kW output on 1,200 mm web width is used just before coating. If corona power exceeds 5 kW, surface oxidation generates low-molecular-weight species that reduce peel adhesion retention after 7 days at 40 °C. Compliance for temporary surface protection films intended for electric appliance panels requires volatile condensable materials below 0.5 wt% as tested by PV 3341 and absence of intentionally added bis(2-ethylhexyl) phthalate under REACH Annex XVII, rows 51–52. The terminal products are 30–50 µm masking films for pre-painted aluminium, acrylic sheet, and brushed stainless steel panels, where the mLLDPE layer contributes conformability around 0.5 mm radius bends without stress whitening.

    Greenhouse Film UV Stabilization Requires a Narrow Processing Window

    For greenhouse cover film at 150 µm total gauge, a five-layer structure is blown on a 70 mm single-screw extruder with 30:1 L/D and 350 mm spiral mandrel die at 2.0:1–2.3:1 blow-up ratio, using 1018MA as the main structural resin in the 30 µm outer layer and 60 µm core layer at 70 wt% total formulation. The remaining 30 wt% comprises a butene-based LLDPE for easier bubble tear in the inner layer and a 4–6 wt% additive masterbatch containing hindered amine light stabilizer at 0.4 wt%, benzotriazole ultraviolet absorber at 0.2 wt%, antifog at 1.2 wt%, and calcium stearate acid scavenger at 0.05 wt% to neutralize catalyst residues that would otherwise accelerate stabilizer consumption at 190–200 °C melt temperature. The processing window is limited by the softening point near 95 °C; barrel temperatures above 210 °C deactivate the benzotriazole absorber via volatilization, reducing UV transmission stability below the 80 % retained tensile elongation threshold required after 4,000 h of QUV testing under ASTM G154 Cycle 1. A die gap of 2.5 mm and frost line height 5 die diameters are used to obtain a lamellar crystal structure that raises infrared retention in the 7–14 µm wavelength band; direct measurement by ASTM E903 for solar transmittance may be used to verify that IR retention remains above 20 % for a single-layer equivalent. The final products are greenhouse cover film and silage stretch cover, with 1018MA selected for puncture tolerance during hail and wind gusts; ASTM D5748 puncture energy on the 150 µm film should not fall below 3 J at 23 °C. Compliance for agricultural plastic in the European market requires conformity to REACH Article 33 communication obligations for substances of very high concern above 0.1 wt%, and the film must not exceed 20 mg/kg chromium, 20 mg/kg cadmium, 20 mg/kg lead, and 20 mg/kg mercury when tested as packaging waste under EN 13432 due to end-of-life mechanical recycling.

    When Hot Tack Is Measured at 40 m/min on a Frozen Food VFFS Line

    Under film draw speeds of 40 m/min on a vertical form-fill-seal machine running 60 packages/min, the sealant layer of a printed biaxially oriented polypropylene/polyethylene laminate for frozen vegetable pouches is 35 µm of 1018MA, coextruded with a 15 µm skin of ethylene-vinyl acetate in a three-layer cast process and subsequently laminated to 18 µm BOPP. On this line, the seal bar dwell time is 30–40 ms, far shorter than the 0.5 s dwell used in laboratory flat-bar heat seal testing under ASTM F88. Under this condition, the seal bar temperature must be set 10–15 °C above the static seal initiation temperature of 95 °C to reach the required hot tack strength. Hot tack is measured under ASTM F1921 at 0.2 N/mm peel force; the 1018MA formulation retains a hot tack strength above 2 N/15 mm at 110 °C to 125 °C, whereas conventional Ziegler-Natta LLDPE of the same density narrows this window by 5–8 °C. Failure on the packaging line occurs when seal initiation drops below 105 °C after the addition of on-spec regrind exceeding 25 wt%, because oxidized regrind particles increase seal initiation temperature and reduce hot tack reproducibility between batches. Low-temperature puncture and flex crack resistance are verified by ASTM D3763 at -30 °C and ASTM F392 Gelbo flex testing for 500 cycles at -20 °C; the laminate must not exhibit pinholes greater than 0.5 mm after flexing. Compliance for frozen food contact is assessed by FDA 21 CFR 177.1520(c) and EU Regulation (EU) No 10/2011, Annex I, with overall migration not exceeding 10 mg/dm² in the appropriate food simulant when evaluated under the test conditions established by EU 10/2011. The terminal products are IQF vegetable pouches, seafood pillow packs, and ice cream side gusset bags, where a 35 µm 1018MA sealant layer is chosen to prevent seal failures at freezer temperatures below -25 °C.

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    Certification & Compliance
    More Introduction

    ExxonMobil Exceed LLDPE 1018MA is a metallocene-catalyzed ethylene-hexene copolymer supplied as pelletized resin for blown-film extrusion. The nominal density is 0.918 g/cm³ under ASTM D1505, and the melt index is 1.0 g/10 min at 190°C/2.16 kg under ASTM D1238. The MA suffix identifies the antiblock/slip additive configuration used to reduce film blocking and control coefficient of friction without post-extrusion surface treatment. The resin is positioned for monolayer and coextruded blown film where seal initiation temperature, impact toughness, and optical clarity determine package performance. The single-site metallocene catalyst generates a narrow molecular weight distribution and uniform comonomer placement, which differentiates the grade from conventional Ziegler-Natta LLDPE produced with multiple active-site populations. Converter-specific film data must be generated on target equipment because die gap, blow-up ratio, frost line height, air-ring geometry, and gauge profile modify final properties.

    Material Specification and Extrusion Identity

    The controlled molecular architecture of 1018MA influences extruder pressure, melt temperature rise, and shear response. The viscosity curve is narrower than that of a broad-distribution Ziegler-Natta LLDPE of equivalent melt index; low-shear viscosity is typically lower, while high-shear viscosity may be similar. In a single-screw grooved-feed extruder with L/D 25:1 to 30:1, pressure generation is directly dependent on screw compression ratio, barrier flight clearance, and screen-pack configuration. Melt temperatures are normally held between 190°C and 240°C, with the lower limit governed by melt pressure limits and the upper limit governed by thermo-oxidative degradation. Melt pressure at the screen pack should be monitored to detect gel accumulation; a rising pressure trend indicates insufficient melt filtration or excessive residence time. The grade does not require pre-drying under normal closed-container storage, but cold pellet surfaces exposed to high humidity can carry surface moisture that produces bubbles in the melt film.

    PropertyTest methodTypical value
    Nominal densityASTM D15050.918 g/cm³
    Melt indexASTM D12381.0 g/10 min at 190°C/2.16 kg
    ComonomerManufacturer technical data sheetEthylene-hexene copolymer
    Catalyst technologyManufacturer technical data sheetMetallocene
    Additive packageManufacturer technical data sheetAntiblock/slip; loadings proprietary

    Shear viscosity data under ASTM D3835 show that 1018MA has a lower degree of shear thinning than broad-molecular-weight-distribution LLDPE. The practical consequence is that high-shear extrusion does not reduce apparent viscosity as strongly, so aggressive mixing screws can generate excessive melt temperature. Melt elasticity and die swell are lower because the high-molecular-weight tail is reduced; this improves melt layer distribution in coextrusion but can reduce melt strength in high-stalk bubble configurations. The onset of sharkskin surface roughness may occur at lower shear stress than in a broad-MWD resin with similar melt index; die lip surface finish and exit geometry are therefore critical for thin-gauge film below 25 µm.

    Cooling-rate sensitivity is a second differentiator. The uniform comonomer distribution produces a narrower crystallization exotherm. On a blown-film line, rapid cooling from the die exit to the frost line freezes oriented chain segments and controls lamellae organization. The frost line height is therefore a primary process variable. If the frost line is too low, the film may exhibit higher machine-direction orientation and splitty tear; if too high, bubble stability and optical clarity can degrade. The optimum frost line height is established by gauge-uniformity mapping and tear-balance measurement per ASTM D1922, not by a single resin property.

    Film property qualification is not derived solely from resin density and melt index. Tensile properties per ASTM D882, dart impact per ASTM D1709, Elmendorf tear per ASTM D1922, haze per ASTM D1003, gloss per ASTM D2457, and seal strength per ASTM F88 are required to establish converter-specific performance. Published data for this specific configuration are limited because final film properties are coupled to die gap, blow-up ratio, frost line height, air-ring turbulence, and cooling rate. The crystallinity developed during bubble cooling is a function of the temperature gradient between the die exit and the frost line, not solely the resin density.

    How Does 1018MA Differ from Conventional Ziegler-Natta LLDPE Grades?

    The difference originates in the catalyst. Ziegler-Natta systems contain multiple active-site types with different propagation and chain-transfer rates. The resulting polymer has a broad molecular weight distribution and a composition distribution in which high molecular weight fractions are more linear. In contrast, the metallocene single-site system used for Exceed 1018MA produces a narrow molecular weight distribution and a uniform short-chain branching distribution. Hexene-derived butyl branches are incorporated more evenly along the polyethylene backbone than butene-derived ethyl branches, which is significant because butyl branches disrupt the orthorhombic crystal lattice more efficiently at equivalent molar concentration. The consequence is that 1018MA can achieve lower density and higher tie-chain concentration without the high linear fractions that increase crystalline lamellae thickness and haze.

    ParameterExceed LLDPE 1018MAConventional Ziegler-Natta C4-LLDPE
    Catalyst technologyMetalloceneZiegler-Natta
    Molecular weight distributionNarrowBroad
    Comonomer distributionUniformHeterogeneous
    Seal initiation temperatureTypically lower; quantified by ASTM F88Higher
    Haze at equal gaugeTypically lower; quantified by ASTM D1003Higher
    Dart impact at equal densityTypically higher; quantified by ASTM D1709Lower
    Elmendorf tear balanceGauge-dependent; quantified by ASTM D1922Gauge-dependent

    In blown film, the practical consequences extend beyond the comparison table. The narrow melting distribution lowers seal initiation temperature and improves hot-tack because the transition from molten to solid is faster after the seal bar opens. Optical haze and gloss are improved by reduced internal crystallite scattering, but surface haze remains controlled by die lip quality, air-ring stability, and frost line turbulence. Machine-direction tear and transverse-direction tear are strongly affected by blow-up ratio and frost line height; published film data cannot be transferred from one line configuration to another without re-qualification. Secant modulus of 1018MA is typically lower than that of a conventional C4-LLDPE of equivalent density when measured per ASTM D882, because the thinner average lamellar thickness reduces the crystalline load-bearing capacity. The reduction in stiffness is offset by increases in dart impact and Elmendorf tear resistance, allowing down-gauging in applications where stiffness is not the controlling design parameter.

    When Seal Integrity and Optical Clarity Constrain Packaging Design

    In high-speed form-fill-seal and vertical packaging lines, sealing dwell times are short and product drop may occur while the seal is still partially molten. The narrow melting distribution of 1018MA promotes rapid solidification after the heating jaw opens, which supports hot-tack performance. Hot-tack strength measured by ASTM F1921 and seal strength measured by ASTM F88 are the relevant qualification tests. The resin is often evaluated in blown film structures with die gaps of 1.8 mm to 2.5 mm and blow-up ratios of 2.0 to 3.0. At 25 µm to 50 µm gauge, optical haze per ASTM D1003 and gloss per ASTM D2457 are used to determine package appearance, but the values depend on air-ring configuration and cooling efficiency. The grade is used in collation shrink, heavy-duty bags, frozen food packaging, and down-gauged films in which machine-direction tear and dart impact must be maintained while film thickness is reduced. Converter trials are required to confirm the seal initiation temperature for specific package formats and production speeds.

    In coextruded sealant layers, slip agents migrate to the surface over time; migration kinetics are affected by layer thickness, temperature, and polymer density. Because slip additives migrate more rapidly in lower-density layers, the coefficient of friction may change after winding and storage. Converters should monitor kinetic coefficient of friction per ASTM D1894 after 24 h and 7 days of aging to ensure that packaging line performance remains consistent. The antiblock/slip package in 1018MA is configured for blown-film conversion; use in cast film or extrusion coating requires evaluation because additive distribution and surface effects differ.

    Production-scale blown-film lines running 1018MA report that bubble instability in high-stalk configurations is most commonly caused by air-ring turbulence, not by resin variability. Batch-to-batch variance in melt index and density is controlled within narrow specification limits, but additive dispersion can vary with handling and conveying conditions. Film converters using vented single-screw extruders with L/D 30:1 and Maddock mixing sections obtain better additive dispersion than those using low-compression general-purpose screws. Screen packs of 20-40 mesh are typical, but finer screens may be required for high-quality surface finish. When melt fracture occurs, reducing melt temperature or increasing die gap can shift the critical shear stress; however, these adjustments also affect tear balance and haze.

    Processing boundaries for 1018MA are set by melt temperature, residence time, and regrind ratio. Melt temperatures above 240°C accelerate oxidation and can generate gel particles; temperatures below 180°C increase melt viscosity and may exceed extruder pressure limits. Regrind addition is normally started at 20% by weight and adjusted based on film appearance and bubble stability. The material is not hygroscopic; drying is not required unless surface condensation occurs from storing cold pellets in high-humidity environments. In coextruded structures, 1018MA must be placed in contact with compatible polyethylene layers; direct adhesion to uncompatibilized polypropylene or EVOH is insufficient and may cause delamination under load. For food-contact applications, the final film must be evaluated against FDA 21 CFR 177.1520 and EU Regulation 10/2011 under the intended conditions of use, and manufacturer compliance documentation should be reviewed before commercial use.

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