Lyondellbasell Icorene 3560 Bue 5111 Polyethylene Linear Low Density

LyondellBasell Icorene 3560 BUE 5111 Polyethylene, Linear Low Density

    • Product Name: LyondellBasell Icorene 3560 BUE 5111 Polyethylene, Linear Low Density
    • Factroy Site: Yinchuan, Ningxia, China
    • Price Inquiry: sales8@ascent-chem.com
    • Manufacturer: Ascent Petrochem Holdings Co., Limited
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    VTB
    Specifications
    HS Code 718652
    Polymer Type Polyethylene, Linear Low Density
    Density 0.935 g/cm³
    Melt Flow Rate 190 C 2 16 Kg 3.5 g/10 min
    Tensile Strength At Yield 14 MPa
    Tensile Strength At Break 24 MPa
    Elongation At Break 700%
    Flexural Modulus 552 MPa
    Vicat Softening Temperature 105 °C
    Melting Point 127 °C
    Hardness Shore D 50
    Deflection Temperature At 0 46 Mpa 70 °C

    As an accredited LyondellBasell Icorene 3560 BUE 5111 Polyethylene, Linear Low Density factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Typically supplied in 25 kg polyethylene-lined paper bags, palletized as 40 bags per 1,000 kg pallet.
    Container Loading (20′ FCL) 20′ FCL container loading: palletized 25 kg bags of LyondellBasell Icorene 3560 BUE 5111 LLDPE, stretch-wrapped, approx. 20–22 MT total.
    Shipping LyondellBasell Icorene 3560 BUE 5111 Polyethylene, Linear Low Density is not classified as dangerous goods for transport. No UN number, hazard class, or packing group required. Ship in original sealed packaging, keep dry, avoid heat, sunlight, and contamination. Follow all local, national, and international transport regulations.
    Storage Store in a cool, dry, well-ventilated area away from direct sunlight, heat, sparks, and flames. Keep original containers or bags tightly closed to prevent moisture pickup, dust, and contamination. Avoid prolonged UV exposure and excessive stacking. Use good housekeeping to control dust and static. Follow the manufacturer's safety data sheet and local regulations. Observe first-in, first-out stock rotation.
    Shelf Life Shelf life is 24 months from production date when stored cool, dry, in original unopened packaging, away from direct sunlight.
    Application of LyondellBasell Icorene 3560 BUE 5111 Polyethylene, Linear Low Density

    When Rotational Moulding Produces Agrochemical Tanks, Wall-Stock Uniformity Governs Chemical Permeation

    In gravity-fed agricultural sprayer and mobile fertigation tank production, LyondellBasell Icorene 3560 BUE 5111 type linear low density polyethylene is dry-blended rather than melt-compounded before entering the biaxial carousel machine. At incoming inspection, melt flow rate is checked under ISO 1133-1:2022 at 190 °C/2.16 kg; a shift greater than 0.5 g/10 min from the lot certificate requires oven setpoint correction of 5–8 °C to maintain the same densification plateau. Compliance for the finished tank is anchored to ASTM D1998-15 hoop-stress design and ISO 175:2000 chemical immersion evaluation using fertilizer-grade aqueous urea at 28% w/w nitrogen, ammonium nitrate 10% w/w, and pH-buffered trace-element mixtures at 40 °C for 90 days; acceptance requires tensile elongation retention above 75% and no environmental stress-cracking when specimens are preconditioned per ASTM D1693-15 Condition B with 10% Igepal CO-630. The dry-blend addition of light-stable color concentrate is normally held at 0.8–1.5 wt%, and supplemental UV masterbatch is restricted to 0.5–1.0 wt% because the BUE 5111 stabiliser package already provides exterior weathering resistance as assessed by retained elongation after ASTM G154-16 exposure. Lubricant-type processing aids above 0.2 wt% are not used because they reduce interparticle fusion at the tool surface and can create low-density weld seams. The production sequence uses a high-speed mixer at 600–800 rpm for 5–8 min to distribute the dry blend, followed by charging into a vented mild steel or cast aluminium tool that is rotated biaxially at 4–6 rpm on the major axis and 1–2 rpm on the minor axis. Oven temperature is controlled at 290–310 °C, and the internal air temperature measured by a wireless thermocouple reaches 190–205 °C; total in-oven dwell is 22–38 min for nominal wall thickness 6–12 mm. The critical processing boundary is the narrow gap between complete densification and oxidative embrittlement: at internal air temperatures above 210 °C or dwell times beyond 45 min, the outer surface becomes brittle because antioxidant consumption accelerates, while below 185 °C the powder particles may sinter but not fully fuse, producing microscopic porosity that increases urea permeation. Finished parts are air-cooled to 85 °C and then forced-air cooled at 5–8 °C/min before demoulding at 55–60 °C. Wall thickness is measured ultrasonically at grid intervals of 300 mm, with a tolerance of ±0.5 mm; the out-of-roundness limit on vertical tank shells is 1.0% of diameter. Terminal articles include cylindrical and rectangular pesticide or fertiliser storage tanks from 100 L to 10,000 L, sprayer induction hoppers, and secondary containment sumps for farm chemical loading stations.

    In subsurface stormwater detention chambers and wastewater inspection manways, the decisive material property is slow crack growth resistance under sustained soil load and occasional surfactant exposure. Raw-material certification for this segment checks the environmental stress-cracking resistance against ASTM D1693-15 Condition B, with a typical acceptance threshold of F50 > 1,000 h, and the finished chamber design follows EN 13598-1:2010 for shallow inspection chambers and AASHTO LRFD live-load provisions for traffic-rated burial depths of 1.0–2.5 m. The dry-blend formulation can include up to 15 wt% of cleaned, same-grade rotomoulded regrind; above 20 wt% regrind the ESCR value drops below design margin and the out-of-flatness on long roof spans increases because regrind reduces the melt plateau. For black or dark grey utility parts, carbon black masterbatch is added at 2–3 wt% to achieve a carbon black dispersion rating of ≤ 2 per ISO 11420:2008. Production uses a rock-and-roll machine for quasi-rectangular chambers with length-to-diameter ratios greater than 2:1; the tool is charged at room temperature, not preheated, and the first-heat cycle raises the internal air temperature to 195–205 °C over 25–32 min. The second axis is set to 3–5 rpm while the main rocking cycle runs at 10–14 s per stroke. The cooling stage is deliberately slow, below 5 °C/min, to reduce differential shrinkage between thick corner radii and thin sidewalls; forced-water cooling is not used on parts taller than 1.2 m because abrupt cooling creates internal vacuum deformation at the roof crown. Terminal articles are stormwater infiltration chambers, septic tank shells, pump chambers, and dry utility vaults rated for pedestrian or H-20 traffic load.

    What Does the ESCR Plateau Mean for Sulphuric Acid Retention in Secondary Containment Pallets?

    Rotational moulding of secondary spill pallets and chemical containment sumps uses the grade’s high-shear-free sintering behaviour to produce unribbed shells with smooth interior corners. The compliance assessment for hazardous-materials containment follows 40 CFR 264.175 for containment volume and freeboard, which requires at least the greater of 10% of total contained volume or 100% of the largest container depending on the site layout. Chemical resistance is tested under ISO 175:2000 with 5% w/w sulphuric acid at 23 °C for 30 days; mass increase must remain below 0.5% and surface whitening is not accepted. For food-adjacent utility pallets, direct food-contact compliance requires verification against 21 CFR 177.1520 olefin polymer extraction limits, though this does not apply once a barrier liner is inserted. Addition ratios are application-specific: conductive carbon black masterbatch is dosed at 4–7 wt% only where static dissipation below 109 Ω surface resistivity is specified; standard chemical containment trays use 1–2 wt% pigment masterbatch and 0–10 wt% same-grade regrind. The production equipment for large shallow trays is a shuttle-type rotomoulding machine with a cast aluminium tool floor thickness of 8–10 mm; internal air temperature is held at 195–210 °C for 18–25 min, followed by air cooling only. The operationally critical failure mode is rib sink on the underside of pallet decks when mould release is sprayed unevenly; this is prevented by restricting release coating to 0.8–1.2 g/m² and monitoring internal air temperature at three zones with a maximum differential of ±7 °C. Terminal parts are low-profile chemical containment pallets, drip trays, laboratory waste sumps, and stackable bulk tote boxes.

    For marine buoy collars and dock fender shells, the processing risk shifts from oxidative degradation to moisture pick-up and uneven cooling of elongated closed bodies. The raw-material powder is stored in sealed containers and conditioned for 24–48 h at 20–25 °C and 40–50% RH before charging; moisture above 0.05 wt% produces surface pockmarks because steam is trapped at the mould-polymer interface. The finished marine component is tested after 1,000 h of accelerated weathering per ASTM G154-16 Cycle 1, with an acceptance limit of ΔE ≤ 3.0 and tensile elongation retention ≥ 70%; water absorption is measured by ISO 62:2008 after 24 h at 23 °C and is expected to remain below 0.1%. The formulation addition consists of 1–2 wt% marine-stable pigment masterbatch; no external hindered amine light stabilisers or antioxidant boosters are normally added because the BUE 5111 package is already intended for exterior weathering. Production of a large fender or buoy shell uses rock-and-roll rotation rather than a carousel; oven set temperature is 280–295 °C, and the internal air temperature is brought to 190–200 °C over 30–40 min, after which cooling is carried out at 3–5 °C/min with infrared surface thermography to detect hot bands. Foam filling is performed after the shell is demoulded and cooled below 40 °C; amine-catalysed polyurethane foam systems are excluded because residual amine can accelerate surface oxidation in the polyethylene shell at the interfacial layer. Terminal articles are rotationally moulded closed-cell foam-filled fenders, floating dock pontoon shells, and slip-resistant buoy bodies.

    Outdoor Furniture Shells: Pigment Opacity, Not Stabiliser Loading, Determines Long-Term Colour Retention

    In playground and street-furniture moulding, the contract specification often imposes both mechanical impact resistance and surface-colour fastness. Compliance is checked against EN 71-3:2019+A1:2021 migration limits for aluminium, antimony, arsenic, barium, boron, cadmium, chromium, cobalt, copper, lead, manganese, mercury, nickel, selenium, strontium, tin, and zinc in the finished article, and against ASTM F1487-17 for impact-attenuating site components where relevant. The addition formula uses 1–3 wt% heavy-metal-free colour masterbatch, with reduced UV absorber addition of 0.2–0.5 wt% only in pastel shades where pigment opacity is below 70%; dark shades do not require additional UV screening because the pigment itself blocks solar radiation. Rotomoulding is performed in a shuttled carousel using aluminium moulds with surface roughness Ra 2–6 µm on the exterior, which produces a matte finish that hides flow lines. Oven setpoint is 270–290 °C, internal air temperature is 185–195 °C, and dwell is 18–25 min for shells with 4–7 mm nominal wall thickness. Demoulding is conducted at 50–60 °C to preserve dimensional control; parts are not stacked while their core temperature exceeds 35 °C. The major failure signal is stress-whitening under impact at temperatures below −10 °C, which is avoided by limiting regrind to 5 wt% in high-impact zones. Terminal parts include seat shells, planter bodies, play panels, and low-height safety barriers.

    Windscreen Washer Reservoirs Fail Through Weld-Line Stress Cracking, Not Impact Puncture

    Under-hood cabin fluid reservoirs are selected for rotomoulding only after blow-moulded alternatives fail wall-thickness capability audits at draw ratios below 35%. The compliance package includes ISO 22241-3:2017 for diesel exhaust fluid handling components where AUS 32 is stored, SAE J2044:2009 for quick-connect fittings, and ASTM D746-20 for brittleness temperature, with brittleness temperature below −40 °C required for cold-climate service. The only permitted external addition is 0.5–1.0 wt% of a non-ester process aid; antifog, antimicrobial, and ester-based slip additives are excluded because under-hood chemical contact tests show surface migration and joint leakage after thermal cycling. Production uses a carousel machine with major-axis rotation 8–10 rpm and minor-axis rotation 2–3 rpm; oven setpoint is 280–300 °C and internal air temperature reaches 195–205 °C over 10–18 min for 2–4 mm nominal walls. Weld lines around brass inserts and quick-connect bosses are formed by preheating the inserts to 90–110 °C before charging; inserting cold hardware below 60 °C creates a low-fusion annulus where stress cracking initiates after 200–400 thermal cycles from −20 °C to 80 °C. Demoulding occurs at 50–60 °C, followed by a 24 h ambient stress-relief rest before pressure leak testing at 30 kPa. Terminal parts are windscreen washer reservoirs, coolant overflow tanks, and diesel exhaust fluid reservoirs for commercial vehicles.

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    Certification & Compliance
    More Introduction

    LyondellBasell Icorene 3560 BUE 5111 is a linear low density polyethylene grade characterized by a density near 0.935 g/cm³ and a melt mass-flow rate near 5.0 g/10 min when measured at 190 °C under a 2.16 kg load. The product belongs to the ethylene-alpha-olefin copolymer family and is supplied as pre-stabilized pellets. The BUE 5111 suffix denotes the additive and stabilization formulation; interpretation should be confirmed against the current LyondellBasell technical datasheet, particularly for food-contact, UV-exposure, or medical end-use qualification. Lot-specific release values for density, flow rate, and additive content are reported on the certificate of analysis.

    Which specification parameters are used for incoming inspection of Icorene 3560 BUE 5111?

    The two primary release properties are density and melt mass-flow rate. Density is measured under ASTM D1505-20 or ISO 1183-1:2019; the typical value for this grade is 0.935 g/cm³. Melt mass-flow rate is measured under ASTM D1238-20 or ISO 1133-1:2022 at 190 °C with a 2.16 kg load; the typical value is 5.0 g/10 min. A density of 0.935 g/cm³ positions the grade between lower-density blown-film resins and higher-density HDPE. The melt flow rate indicates a moderate-flow processing window; it is not a fractional-melt grade for large blow-molded parts and not a very high-flow thin-wall packaging resin. Additional properties reported for the product include tensile strength at yield, elongation at break, flexural modulus, Vicat softening temperature, and environmental stress crack resistance. Table 1 lists representative distributor-reported values. These values are control targets, not batch specifications; incoming inspection limits should be taken from the supplier’s purchase specification.

    PropertyTest methodTypical valueUnit
    DensityASTM D1505-20 / ISO 1183-1:20190.935g/cm³
    Melt mass-flow rateASTM D1238-20 / ISO 1133-1:20225.0g/10 min
    Tensile strength at yieldASTM D638-1417.0MPa
    Elongation at breakASTM D638-14800%
    Flexural modulusISO 178:2019 / ASTM D790-17650MPa
    Vicat softening temperatureISO 306:2022 A50122°C
    Environmental stress crack resistanceASTM D1693-15, Condition B, 100% Igepal>1000h

    Although fully disclosed multi-axial impact data for this exact BUE 5111 configuration are limited in open databases, the resin class behavior is well documented: an LLDPE with density near 0.935 g/cm³ and butene comonomer typically shows a balance of stiffness and ESCR, with lower dart impact and tear resistance than an octene LLDPE at equivalent density. Infrared spectroscopy is used to identify comonomer type and concentration because density and melt flow rate alone do not distinguish butene from hexene or octene. Differential scanning calorimetry is used to measure melting behavior; a typical peak melting point for a 0.935 g/cm³ ethylene-butene LLDPE is near 126 °C. Crystallinity calculated from melt enthalpy should use a reference value of 293 J/g for fully crystalline polyethylene.

    Where the grade is used in injection molding, the melt temperature should be maintained between 190 °C and 240 °C. Residence time above 240 °C should be minimized because thermomechanical degradation can lead to gel formation and gloss loss. On a single-screw extruder with L/D 25:1 to 30:1, a general-purpose polyolefin screw with a compression ratio of 2.5:1 to 3.0:1 is adequate. Pre-drying is not routinely required at ambient humidity below 60% RH; however, condensation on cold pellets can cause surface splay. In rotational molding, if the grade is pulverized to 35 mesh, the cook cycle should be designed to bring the internal air temperature to 200–210 °C before controlled cooling. Densification and bubble removal are influenced by the resin’s zero-shear viscosity and narrow molecular weight distribution relative to LDPE. Batch-to-batch shifts in melt flow rate of ±0.5 g/10 min can alter fill time in thin-wall tools and should be monitored.

    The solidification behavior of the grade is governed by density and comonomer distribution. At cooling rates encountered in injection molding, the material forms spherulitic morphology with lower nucleation density than high-density polyethylene. For thin-wall parts, mold temperatures below 30 °C increase frozen-in orientation and can improve clarity but reduce impact. For thicker sections, cooling-rate gradients produce a skin-core structure; the skin layer has lower crystallinity because of rapid quenching, while the core develops higher shrinkage. Post-molding dimensional stability can be improved by annealing at 80–100 °C for 2 h, but this is not required for most applications.

    When this product is substituted for an autoclave LDPE or a fractional-melt HDPE, what operational adjustments become necessary?

    LLDPE does not exhibit the same degree of shear thinning as autoclave LDPE because it lacks the same long-chain branching architecture. As a result, head pressure and back pressure may increase at equivalent throughput. Set-point temperatures may need to be raised within the 200–230 °C band to reduce melt viscosity, but the maximum melt temperature should remain below 260 °C to avoid oxidative chain scission. Compared with a fractional-melt HDPE used for large structural parts, the 5.0 g/10 min melt flow rate improves fill velocity and surface detailing but reduces melt strength; this can affect wall uniformity in blow molding and rotational molding. Dimensional shrinkage is also different: the 0.935 g/cm³ density produces lower volumetric shrinkage than a 0.918 g/cm³ film grade and higher shrinkage than a 0.952 g/cm³ HDPE. Tooling dimensions should be adjusted using the coefficient of linear thermal expansion and mold shrinkage data from the manufacturer’s datasheet, not from generic LLDPE averages.

    In the polyolefin product hierarchy, the choice between butene, hexene, and octene LLDPE is governed by branch length. Butene incorporation creates ethyl branches, hexene creates n-butyl branches, and octene creates n-hexyl branches. Longer branches increase tie-chain probability at equivalent comonomer content, which generally improves impact toughness, tear resistance, and ESCR. Where the BUE suffix corresponds to a butene comonomer, as is common in LyondellBasell ethylene polymer nomenclature, a butene LLDPE of this type is selected when the process window and cost structure favor moderate impact performance and higher modulus. Table 2 summarizes the class-level comparison. The values are typical ranges, not grade-specific release limits.

    Butene Comonomer Architecture and Property Trade-Off Against Hexene and Octene Grades

    The molecular difference between comonomer types is small in monomer concentration but significant in solid-state performance. At equal density and melt flow rate, a butene LLDPE has shorter branches than a hexene or octene LLDPE. The shorter branches are less efficient at connecting adjacent lamellae, so the butene grade may show lower dart impact, lower Elmendorf tear, and lower slow crack growth resistance. The advantage is often higher flexural modulus and lower resin cost. This does not make the butene grade inferior in absolute terms; it makes it appropriate for applications where the load is primarily tensile or flexural and where the part is not subjected to repeated low-temperature impact.

    Resin classShort-chain branchDensity rangeMelt flow rate rangePractical limitation
    Autoclave LDPElong-chain branching0.910–0.925 g/cm³0.2–70 g/10 minLower modulus and heat resistance
    Butene LLDPEethyl branches0.915–0.940 g/cm³0.5–20 g/10 minLower impact toughness than octene LLDPE
    Hexene/octene LLDPEn-butyl / n-hexyl branches0.915–0.940 g/cm³0.5–20 g/10 minHigher cost and slightly lower stiffness at equal density
    HDPEminimal short-chain branching0.941–0.965 g/cm³0.1–30 g/10 minReduced ESCR relative to LLDPE at high density

    Storage conditions for polyethylene are frequently under-specified. Icorene 3560 BUE 5111 should be stored in a dry area below 50 °C and protected from direct sunlight. Long-term outdoor storage of packaged material can raise pellet surface temperature and consume the antioxidant package. If sacks are stored for more than 12 months, oxidation induction time should be checked by ISO 11357-6 or ASTM D3895-19. The additive package is intended to protect the resin during melt processing, not to serve as a substitute for post-fabrication UV stabilizer in the finished article unless the grade suffix explicitly designates a UV-stabilized formulation.

    Food-contact evaluation for this grade falls under FDA 21 CFR 177.1520 when the finished article meets the applicable extractive limitations. European compliance is commonly assessed under Regulation (EU) No 10/2011, including an overall migration limit of 10 mg/dm² for general food-contact applications. The product is supplied with a safety data sheet and may be subject to REACH registration obligations; the specific registration number, end-use restrictions, and organoleptic performance should be confirmed with LyondellBasell before commercial use in food packaging or potable water systems.

    Operational boundaries follow from the combination of butene LLDPE rheology and stabilizer package. Do not hold the melt at temperatures above 260 °C for prolonged periods, and avoid direct dry-blending with amine-functional additives unless the stabilizer system is explicitly designed for such combination; certain hindered amine light stabilizers are known to antagonize phenolic antioxidants. Outdoor weathering should be validated according to ISO 4892-2 or ASTM D2565-23 at the intended wall thickness because UV performance is thickness-dependent. If the material is reground, the regrind content should be controlled and tested for melt flow drift because LLDPE is sensitive to shear-induced chain scission at high processing temperatures.

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