| HS Code | 912182 |
| Density | 0.935 g/cm³ |
| Melt Index | 0.8 g/10 min (190°C/2.16 kg) |
| Comonomer | Butene-1 |
| Additive | Slip and Antiblock |
| Melting Point | 124 °C |
| Vicat Softening Temperature | 105 °C |
| Tensile Strength At Yield | 11.7 MPa |
| Tensile Strength At Break | 22.1 MPa |
| Elongation At Break | 700% |
| Flexural Modulus | 310 MPa |
| Hardness Shore D | 50 |
| Dart Drop Impact | 200 g |
| Elmendorf Tear Strength | 300 g |
| Haze | 8% |
| Gloss | 70% |
As an accredited LyondellBasell Icorene 3560 BUE 5908 Polyethylene, Linear Low Density factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | LyondellBasell Icorene 3560 BUE 5908 is supplied in 25 kg polyethylene-lined paper bags, palletized and stretch-wrapped for secure shipment. |
| Container Loading (20′ FCL) | 20′ FCL container loading of LyondellBasell Icorene 3560 BUE 5908 LLDPE in 25 kg bags, palletized and secured for transport. |
| Shipping | LyondellBasell Icorene 3560 BUE 5908 Polyethylene, Linear Low Density is shipped as non-hazardous solid resin pellets in 25 kg bags, octabins, or bulk containers. Transport in clean, dry vehicles; protect from moisture, contamination, excessive heat, and UV. No special dangerous goods labeling required under normal conditions. |
| Storage | Store in a cool, dry, well-ventilated area away from direct sunlight, heat, sparks, and open flames. Keep containers or bags sealed to prevent moisture and contamination. Avoid contact with strong oxidizers. Protect from ultraviolet light and excessive stacking. Store indoors on pallets in original packaging. Maintain normal ambient temperatures, use first-in, first-out stock rotation, and keep away from incompatible materials. |
| Shelf Life | Shelf Life: 24 months when stored in a dry, cool area in original unopened packaging, protected from direct sunlight and heat. |
In potable water tank rotomoulding, the linear low density polyethylene powder such as Icorene 3560 BUE 5908 is dry-blended with a phenolic/phosphite stabilizer package before pulverization; the target top size is 35 mesh (500 µm) with a fines fraction below 150 µm controlled to 10–15 wt%. The mould is cast aluminium or machined steel, with wall thickness allowance from 6 mm to 10 mm for vertical tanks up to 5,000 L. A carousel rotomoulding machine with a 4.0:1 mould rotation ratio operates at oven air temperatures between 270 °C and 290 °C; the peak internal air temperature must reach 190–205 °C and remain there for 8–12 min to densify weld lines around moulded-in inserts. Lower peak internal air temperature values generate microporosity at the inner wall; higher values increase oxidative degradation risk measured by melt-flow-rate drift under ISO 1133-1:2022.
Long-term hydrostatic crack initiation is the primary failure criterion for potable water tanks. Lot acceptance for environmental stress crack resistance uses ASTM D1693-15, Condition B, 10% Igepal CO-630, 50 °C; the F50 value from the supplier’s certificate is compared with the tank designer’s minimum. Potable water contact is assessed under NSF/ANSI 61, and food contact uses 21 CFR 177.1520(c) or EU 10/2011 with an overall migration limit of 10 mg/dm². Finished tank pressure and design evaluation follows AS/NZS 4766 or ASTM D1998-15 depending on market. When CNC-machined steel moulds replace cast aluminium, heat transfer changes by 15–25%; the same peak internal air temperature may not produce equivalent densification. Published data for this specific grade in that tooling configuration is limited, so instrumented trial mouldings with internal air probes are required.
The controlling factor for agricultural chemical storage shifts from hydrostatic creep to environmental stress cracking caused by surfactants, solvent carriers and oxidising chlorine cleaners. Rotational moulders dry-blend the powder with a carbon black masterbatch to reach 2.0–2.5 wt% carbon black for outdoor UV resistance; dispersion is checked by compression-moulded plaque surface appearance and by particle sieving before charging. The mould is configured with flat side walls and a large open-top neck; wall thickness is typically 6–12 mm on tanks from 200 L to 10,000 L. Chemical compatibility of the finished wall is evaluated by immersion per ASTM D543-20 using the specific formulated chemical at the field concentration; acceptance is based on visual cracking, mass change and tensile yield retention after 7 days at 23 °C or at the service temperature.
The top flange weld-line area is the most frequent fracture initiation site in drop testing from 1.2 m at -10 °C; instrumented puncture uses a striker conforming to ISO 6603-2:2023. Low-temperature notched impact is measured by ISO 179-1:2023 on specimens cut from the wall at -30 °C, with acceptance defined in the moulder’s PPAP because lot-to-lot variation has a stronger influence than nominal resin grade. If the tank is stacked outdoors, UV weathering is assessed under ISO 4892-2 with xenon-arc exposure and the retention of elongation at break is monitored after 8,000 h; published data for this specific carbon black-loaded grade in a ten-year agricultural service environment is limited.
| End use | Standard / method | Condition | Limit / criterion |
|---|---|---|---|
| Potable water | NSF/ANSI 61 | extraction at pH 5 and pH 8 | no contaminant above single-product action level |
| Food contact | EU 10/2011 | overall migration, simulant A/B/D2, 10 days at 40 °C | 10 mg/dm² |
| ESCR | ASTM D1693-15 | Condition B, 10% Igepal, 50 °C | batch F50 per supplier certificate |
| Notched impact | ISO 179-1:2023 | -30 °C, machined from finished wall | minimum set in moulder PPAP |
| Chemical immersion | ASTM D543-20 | 7 days, field concentration | no visual cracking; tensile yield retention per moulder specification |
Before any fuel or chemical compatibility test is performed on a 10,000 L diesel storage tank, wall thickness uniformity is characterised on twin-arm shuttle machines with 8–15 mm wall sections. The aluminium or steel mould is heated until the peak internal air temperature plateaus at 190–205 °C; then cooling is initiated with forced air, water mist, or a sequenced air-water cycle. Rapid forced-air cooling reduces warpage but increases internal stress at top corners, whereas slow oven cooling reduces stress but extends cycle time by 20–35%. This trade-off is controlled by monitoring mould temperature at the parting line and by measuring wall thickness with ultrasonic gauging after demoulding. Published data for this specific LLDPE grade in twin-arm shuttle cooling profiles is limited, so process qualification relies on instrumented trial runs.
Neat linear low density polyethylene is not a high-barrier fuel resin. Where evaporative emission limits apply under UN ECE R34, the rotomoulded fuel tank must be fluorinated or moulded as a multi-layer structure. Surface fluorination changes the internal surface energy and reduces hydrocarbon permeation, but it requires post-moulding treatment under controlled vacuum/pressure cycles and is not a replacement for wall thickness uniformity. Chemical intermediate storage tanks for dilute sodium hypochlorite or ferric chloride are evaluated under ASTM D543-20; concentrated nitric acid, hot aromatic solvents and strong oxidising environments are outside the normal operating boundary for this polyolefin unless published compatibility data for the specific service concentration and temperature are available.
Outdoor leisure shells and playground components do not rely on hydrostatic pressure but on thin-wall impact toughness and colour retention. The powder is dry-coloured with a masterbatch containing rutile titanium dioxide or selected organic pigments; typical masterbatch addition is 2–4 wt%, but the exact let-down is adjusted to the masterbatch supplier’s pigment loading. The mould is a cast aluminium clam-shell with wall sections from 4 mm to 8 mm. Foam filling of double-wall kayak hulls is performed by introducing a chemical blowing agent after the outer skin has sintered; the peak internal air temperature is kept below 205 °C to avoid premature decomposition of azodicarbonamide where that blowing agent is selected. Adhesion of polyurethane topcoats or pressure-sensitive graphics to the nonpolar polyethylene surface requires flame treatment or atmospheric plasma to raise surface energy from 30–32 mN/m to at least 38 mN/m. Without this step, delamination occurs under cyclic thermal expansion, even when the substrate is intact.
Cold-impact qualification for kayak hulls is performed by ISO 179-1:2023 at -20 °C on specimens cut from the hull wall; acceptance is set in the moulder’s PPAP rather than derived from resin datasheet values. Playground components are assessed against EN 71-3 for migration of heavy metals and against ASTM F1487-21 for impact attenuation of the assembled structure; the polyethylene shell itself is a component, not the fall surface, so a separate impact-absorbing surface may be required.
Food processing tubs are moulded with a double-wall cavity that is subsequently filled with rigid polyurethane foam. The inner contact surface is evaluated against 21 CFR 177.1520 and EU 10/2011; if the tub holds whole fish or brine at 0–4 °C, the moulded wall must not embrittle after repeated thermal cycling from -20 °C to 60 °C. The ethylene-butene comonomer distribution in the linear low density polyethylene retains ductility below -20 °C, but actual lot-to-lot impact variation must be confirmed by ISO 179-1:2023 at -30 °C on specimens cut from the thickest wall. The rotomoulding cycle uses a lower oven air temperature of 250–270 °C and a longer plateau at 190–200 °C to prevent foam core collapse when the second wall is sintered. If the foam fill is injected after demoulding, the inner wall must be cooled to below 50 °C before foam injection to avoid exotherm-induced sink marks.
For direct contact with fish oil and brine, environmental stress cracking per ASTM D1693-15 is not sufficient as the sole qualification; immersion in 3% acetic acid and 10% sodium chloride solutions is often specified by processors. Published data for this specific LLDPE grade in fish oil at 4 °C is limited, so a food processor should perform a worst-case shelf-life migration study using the finished tub geometry and brine fill. The exterior surface may require pressure washing with alkaline detergents; chemical resistance of the outer skin to 1–2% sodium hydroxide at 60 °C is assessed by ASTM D543-20 if the tub is used in sanitary processing lines.
For electronics manufacturing, material handling bins are compounded with conductive carbon black to achieve electrostatic discharge protection. The target surface resistivity for an ESD tote is 10³–10⁶ Ω measured per IEC 61340-2-3, and the finished product must be evaluated under IEC 61340-5-1 for ESD-protected areas. The rotomoulding powder is dry-blended with a conductive carbon black masterbatch; dispersion quality is checked by compression-moulding a plaque and measuring surface resistivity at 12% relative humidity and 23 °C, because low humidity changes the carbon black network stability. The wall thickness of 3–5 mm is lower than tank sections, but flatness is critical for automated conveyor indexing; cooling rates are therefore profiled to reduce edge curl. The bin is assembled with injection-moulded handles or metal hinges only after the rotomoulded shell has stabilised dimensionally for 24–48 h at 23 °C.
Compliance for electronics packaging includes RoHS 2011/65/EU and the REACH candidate list; carbon black is not a heavy metal, but reclaimed content must be traceable to avoid restricted substances. Cleanroom use under ISO 14644-1 may require additional cleaning and particle-shedding evaluation because carbon black-loaded polyethylene can release micro-particles if the surface is abraded. The standard resin is not inherently static dissipative; without carbon black, the surface resistivity is above 10¹² Ω, making the part unsuitable for ESD-protected areas.
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LyondellBasell Icorene 3560 BUE 5908 is classified as a linear low-density polyethylene produced through low-pressure coordination copolymerization of ethylene with an α-olefin comonomer. The numeric string 3560 is interpreted through the manufacturer’s grade-coding system as a density/melt flow position within the Icorene rotational moulding portfolio, while the suffix BUE 5908 identifies a formulated stabilization package. Published certificate-of-analysis data for this specific configuration are limited; batch-level release documents and the supplier’s technical data sheet therefore remain the controlling references for specification compliance. The material is supplied in stabilised powder form for low-shear, thick-section fabrication, and its architecture is distinct from high-pressure LDPE and higher-crystallinity HDPE in both molecular structure and process response.
Density is measured under ISO 1183-1:2019 and is positioned near 0.935 g/cm³; the melt mass-flow rate under ISO 1133-1:2022 at 190 °C with a 2.16 kg load falls into the medium-flow region associated with the 3560 numeric suffix. A density near 0.935 g/cm³ places the grade at the upper end of the LLDPE interval and the lower end of medium-density polyethylene. This shifts the balance toward flexural stiffness and creep resistance while retaining low-temperature ductility. In rotational moulding, release decisions are not limited to melt flow; they also require control of particle size distribution, dry flow, environmental stress-crack resistance, and impact after slow cooling. The screening envelope in the table below is not a release specification for this exact suffix; it is a typical range for a 0.935 g/cm³ LLDPE rotational moulding grade and must be replaced by batch-specific values from the certificate of analysis.
| Property | Standard | Typical screening envelope |
|---|---|---|
| Density | ISO 1183-1:2019 | 0.930–0.940 g/cm³ |
| Melt mass-flow rate | ISO 1133-1:2022 | 5.0–6.5 g/10 min |
| Tensile yield stress | ISO 527-2:2012 | 16–20 MPa |
| Flexural modulus | ISO 178:2019 | 600–850 MPa |
| Environmental stress-crack resistance | ASTM D1693-B | > 500 h |
| Low-temperature instrumented impact | ISO 6603-1:2000 | 8–14 J at -20 °C |
On a three-arm carousel rotational moulder with an oven chamber maintained at 280 °C to 320 °C, the main process conflict is between pore-free densification and surface oxidation. The powder is charged into a biaxially rotating cast aluminium or fabricated steel mould; heat transfer through the mould shell drives melting and coalescence of the LLDPE powder. Peak internal air temperature is typically brought to 190 °C to 210 °C for a 0.935 g/cm³ LLDPE. Exceeding the upper boundary by more than 10 °C may initiate carbonyl formation and discolouration in thick sections. Oven residence time is not a primary control variable; it is adjusted against mould mass, wall thickness, oven set-point, and charge weight to reach the target peak internal air temperature without overshoot.
Dry flow is measured under ISO 6186:2023 using a funnel orifice of 12 mm; flow times below 35 s/100 g are typical for reliable filling of multi-cavity moulds. Particle size distribution is controlled through the 500 µm screen fraction. Excessive fines increase dust accumulation and produce uneven wall thickness, while coarse fractions reduce particle coalescence and can leave internal porosity. Storage at relative humidity above 60 % can cause superficial moisture adsorption on the powder surface; if cold powder is charged into a warm mould, condensation can form and generate pinholes. Pre-conditioning in a warm-air hopper at 40 °C to 50 °C before charging is used to reduce surface moisture.
The density near 0.935 g/cm³ corresponds to a crystalline fraction of approximately 55–60 % when calculated from the two-phase density model using 0.855 g/cm³ for the amorphous phase and 1.000 g/cm³ for the crystalline phase. Rotational moulding applies a low cooling rate, which shifts the lamellar thickness distribution upward. Parts can therefore exhibit higher flexural modulus than the powder nominal value if cooling is excessively slow, but slow cooling also increases spherulitic growth and may reduce impact resistance. Forced-air cooling at 8 °C/min to 12 °C/min from demoulding temperature to 80 °C is used to balance warpage control and toughness.
The BUE 5908 stabilizer package can be characterised by oxidative induction time under ISO 11357-6:2023. Rotational moulding grades with UV stabilization typically exhibit an oxidation induction time at 200 °C of at least 20 min in the as-supplied powder. After one oven cycle, consumption of phenolic and phosphite stabilizer components lowers the measured oxidation induction time. A drop below 5 min after a single cycle indicates that the process has exceeded the thermal stabilizer budget and may produce parts with reduced service life. Production-scale rotational moulding of UV-stabilized LLDPE has shown two recurring failure modes: surface pinholes at sharp male corners and undercut regions, and bubble formation at the inner surface when peak internal air temperature is reached too rapidly. Both are process failures rather than intrinsic material defects; they can be reduced by limiting the heating rate below 8 °C/min during the final 30 °C of mould temperature rise and by increasing the rotation ratio to improve powder distribution.
Unlike high-pressure LDPE, which contains long-chain branching from free-radical polymerization, the Icorene 3560 architecture consists of a linear backbone with short-chain branches derived from the α-olefin comonomer. This difference changes melt rheology: LDPE exhibits greater shear thinning and lower extensional viscosity in low-shear processes, while LLDPE exhibits a broader melting range and a higher plateau modulus after crystallisation. In thick-section parts, the slow cooling rate of rotational moulding magnifies crystallinity effects. A 0.935 g/cm³ LLDPE produces higher flexural stiffness than a 0.918 g/cm³ LDPE but generally exhibits less warpage tendency than HDPE when wall thickness is uniform. Environmental stress-crack resistance of the LLDPE grade is typically superior to that of HDPE with the same nominal melt flow, as measured by ASTM D1693-B; the precise value is batch- and cooling-rate-dependent.
Within LLDPE copolymers, the α-olefin length controls the short-chain branching distribution. Butene comonomer places ethyl branches on the backbone, hexene adds butyl branches, and octene adds hexyl branches. For a given density and melt index, longer branches increase tie-molecule concentration and improve dart impact resistance under ASTM D1709-16a and Elmendorf tear under ASTM D1922-15. A butene-based grade may therefore show lower film tear resistance than a hexene- or octene-based grade, but rotational moulding powder processes place a higher weight on low-shear coalescence and environmental stress-crack resistance, where the differences are less pronounced. The suffix BUE 5908 does not identify the comonomer type; the comonomer should be confirmed from the supplier’s technical declaration if the part is intended for aggressive chemical immersion.
At 190 °C, the low-shear complex viscosity of a 0.935 g/cm³, 6.0 g/10 min LLDPE is typically in the range 1.0 kPa·s to 1.5 kPa·s at 0.1 rad/s under ISO 6721-10:2021. This is lower than a film-extrusion LLDPE of 1.0 g/10 min, allowing lower peak torque and faster coalescence in low-shear processes. Melt strength is also reduced, which becomes relevant if the grade is used in monolayer blown film; the allowable blow-up ratio is lower than for high-pressure LDPE. The higher stiffness of the 0.935 g/cm³ grade can permit a wall-thickness reduction of approximately 10–15 % relative to a 0.918 g/cm³ LLDPE for the same flexural creep requirement under ISO 899-2:2003, provided the part remains in the linear viscoelastic region.
Applications for this class of UV-stabilized LLDPE include outdoor storage tanks, agricultural sprayer tanks, water-management chambers, and thick-section hollow parts where low-temperature ductility and weathering resistance are specified. In outdoor exposure, stabilizer performance is evaluated under ISO 4892-2:2013 xenon-arc weathering with a black-standard temperature of 65 °C or through ASTM G154-16 fluorescent UV exposure. Lot-specific colour change and tensile property retention limits must be defined by the part specification because the BUE 5908 package alone does not guarantee a fixed number of years of service. For potable water contact, compliance is assessed under EN 12873-1 and national implementation rules; for food contact, FDA 21 CFR 177.1520 provides a starting point only if the manufacturer’s food-contact designation is active and applicable. REACH and RoHS compliance are substance-level declarations; polyolefin resin grades do not fall under a single exemption without review of the full formulation.
| Compliance domain | Reference standard or regulation | Required verification |
|---|---|---|
| EU RoHS | 2011/65/EU Annex II | X-ray fluorescence screening if recycled feedstock is used |
| EU REACH | 1907/2006 SVHC candidate list | Safety data sheet and SVHC declaration review |
| Food contact | FDA 21 CFR 177.1520 | Supplier food-contact letter and use limitations |
| Potable water | EN 12873-1 | Migration testing and national acceptance |
| Outdoor weathering | ISO 4892-2:2013 | Delta E, tensile property retention, and surface bloom evaluation |
The material is not suitable for continuous immersion in strong oxidizing acids, halogenating solvents, or aromatic hydrocarbons without chemical resistance data under ISO 175:2010. UV stabilizers with low molar mass can migrate to the surface during outdoor exposure. The BUE 5908 additive package is expected to include hindered amine light stabilizer or benzotriazole class components; migration is assessed by extraction or by monitoring surface bloom after accelerated weathering under ISO 4892-2:2013. Additive migration is governed by the diffusion coefficient in the amorphous phase and increases with temperature. For dark-coloured parts exposed to direct sunlight at surface temperatures above 60 °C, surface depletion can occur before bulk stabilizer exhaustion; this is a known limitation of outdoor polyethylene formulations.