| HS Code | 373046 |
| Density | 0.935 g/cm³ |
| Melt Flow Rate 190 C 2 16 Kg | 3.5 g/10 min |
| Melting Point | 124 °C |
| Vicat Softening Point | 100 °C |
| Tensile Strength At Yield | 11 MPa |
| Tensile Strength At Break | 26 MPa |
| Elongation At Break | 800% |
| Flexural Modulus | 290 MPa |
| Dart Drop Impact | 120 g |
| Haze | 10% |
| Gloss | 80% |
| Brittleness Temperature | < -70 °C |
As an accredited LyondellBasell Icorene 3560 BUE 5123 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 5123 is supplied in 25 kg polyethylene bags, palletized and shrink-wrapped; 1,000 kg bulk bags available. |
| Container Loading (20′ FCL) | 20′ FCL loading: LyondellBasell Icorene 3560 BUE 5123 LLDPE, palletized bags in dry container, evenly distributed, secured for transport. |
| Shipping | LyondellBasell Icorene 3560 BUE 5123 is a non-hazardous, linear low-density polyethylene resin supplied as solid pellets. Typical shipping: 25 kg polyethylene bags or octabins on pallets, or bulk trucks, railcars, or containers. Keep sealed, dry, and clean during transport; avoid heat, UV, moisture, and contamination. Not classified as dangerous goods. |
| Storage | Store LyondellBasell Icorene 3560 BUE 5123 Polyethylene, Linear Low Density in a cool, dry, well-ventilated area away from direct sunlight, heat, sparks, and flames. Keep in original sealed packaging to protect from moisture, dust, and contamination. Avoid contact with strong oxidizers. Stack securely to prevent falling or bag damage. Use appropriate grounding to control static during handling. |
| Shelf Life | Shelf life is typically 24 months when stored unopened in a cool, dry place, away from direct sunlight and heat. |
In rotomolded vessels handling 12.5% sodium hypochlorite at ambient temperature, the dominant failure mode is environmental stress-crack propagation at the inside radius of the top knuckle and the drain fitting. Icorene 3560 BUE 5123 is assigned to this service only when a finished wall sample survives 1000 h in 100% Igepal CO-630 at 50 °C under ASTM D1693-15 Condition A, since sodium hypochlorite represents a more severe stress-cracking medium than potable water. Rotational molding of a 5,000 L vertical tank uses a steel or cast-aluminum mold with a forced-air convection oven set point of 280–300 °C, a measured peak internal air temperature (PIAT) of 202–208 °C, and a residence time of 18–24 min for a nominal wall of 6–8 mm. Exceeding 210 °C PIAT initiates thermo-oxidative chain scission in LLDPE, raising the carbonyl index measured by FTIR per ASTM D5576 and reducing notched Charpy impact according to ISO 179-1/1eA at 23 °C. The powder must exhibit dry flow below 35 s per 100 g and a retained 35 mesh (500 µm) fraction not exceeding 15%; otherwise bridge packing in the mold shoulder produces thin-wall bands below 3 mm. Internal regrind is limited to 20% after cryogenic grinding and sieve homogenization, because higher regrind fractions shift the zero-shear viscosity measured by rotational rheometry at 190 °C and require a 5 °C rise in PIAT to restore full surface replication. Finished tanks are pressure-tested to 34.5 kPa (5 psi) internal air and inspected for pinholes in the bottom drain area per ASTM D1998-21. The end product is an integrally molded chemical storage tank, typically from 200 L to 10,000 L, with no weld line and uniform wall distribution suitable for sodium hypochlorite dosing, detergent concentrates, and low-viscosity agricultural chemicals at ambient service.
Fertigation reservoirs exposed at elevations above 1,500 m require a stabilizer package that remains active through repeated thermal cycles in the rotomolding process. A 10,000 L vertical cone-bottom tank is molded with a wall thickness of 7–10 mm and an internal air pressure of 10–20 kPa during the cooling phase to prevent flat-panel sink marks on the cylindrical shell. The powder is charged at 100 parts base resin to 0.2–0.5 parts UV masterbatch when additional pigmentation is required; pigment loadings above 1.0 part consistently reduce dart impact measured by ASTM D3763 in the -5 °C to 0 °C range, so dark green and black tanks are specified only with the manufacturer's pre-stabilized formulation. Oven dwell at 195–205 °C PIAT is sufficient for a 35:1 arm ratio and a primary-to-secondary axis speed ratio of 4:1. Accelerated xenon-arc exposure under ASTM D2565-23 at 0.35 W/m² at 340 nm should not reduce tensile elongation below 50% absolute after 3,000 h; field data from rotomolding lines indicate that water-quench cooling after demolding restores surface gloss but does not recover lost stabilizer activity. Water-contact compliance is evaluated under EU Regulation 10/2011, FDA 21 CFR 177.1520, and NSF/ANSI/CAN 61 where potable storage is claimed. The end articles are 500–20,000 L water storage and fertigation tanks with integrally molded manway lids and threaded outlet bosses, used in drip irrigation systems where cyclical filling and long UV exposure impose higher stress-cracking demand than indoor storage.
Because brackish-water mooring hardware is subject to repeated compression set and low-velocity impact against quay walls, the rotomolded shell of a foam-filled buoy is processed thicker at the equatorial seam than at the top lifting eye. A 25 mm nominal wall at the seam tapers to 8 mm at the top, requiring a two-stage oven profile: an initial 12 min at 290 °C to densify the powder in the seam region, followed by 8 min at 260 °C to avoid polymer degradation in the thin lifting-eye boss. The LLDPE shell must survive 500 h salt spray exposure per ISO 9227 without cracking and maintain a notched Izod impact above 25 kJ/m² at -20 °C under ISO 180/A. Water absorption is specified below 0.01% by ASTM D570-22 after 24 h immersion; this low absorption prevents freeze-thaw damage when the buoy is lifted onto a deck at sub-zero ambient temperatures. Polyurethane foam filling at 2.5–4.0 parts water to 100 parts polyol is injected after shell cooling, and the exothermic foam rise must not exceed 80 °C at the shell inner wall, measured by a thermocouple embedded at the shell inner surface; if this threshold is exceeded the LLDPE locally recrystallizes and loses impact strength. The terminal buoy product is fitted with a galvanized steel central tube overmolded into the shell; no adhesive bond line is used because the PE shell does not accept structural adhesives without plasma surface activation to 40–50 mN/m wetting tension. Commercial production employs closed molds on a shuttle rotomolding machine with a 2:1 arm ratio, water-spray cooling after forced air, and a total cycle of 45–60 min per cavity.
Diesel exhaust fluid storage for off-road and auxiliary power equipment imposes a contaminant limit because the 32.5% urea solution is sensitive to leached metal ions and organic residues. The rotomolding grade is evaluated for extractables in deionized water at 80 °C for 24 h; total organic carbon release is controlled below 10 mg/L in internal qualification protocols aligned with ISO 22241-3:2019. A 57 L tank with integrally molded baffles and a rotomolded-in HDPE filler neck is produced from virgin powder only; regrind is excluded in this segment because even 5% recycled material raises the variability of trace extractables and shifts the PIAT window by 3–5 °C. The mold configuration uses a 3:1 rotation ratio and a peak internal air temperature of 200–206 °C for 16–20 min, with a 4 mm nominal wall at the lower sump and 6 mm at the corner radii. Low-temperature drop impact is tested per ASTM D2463 using a 9.1 kg dart at -10 °C from 1.8 m, and the part must not show brittle fracture in the sump region. The end product is a rotomolded DEF reservoir with no weld seam in the lower wetted area, fitted with a level sender port and a 2-inch threaded boss. External bracket attachment is made by bolted stainless steel straps rather than adhesive bonding, because LLDPE lacks polar surface functionality without plasma or flame treatment.
In dry bulk powder handling, static dissipation directs resin selection toward non-fuel-contact polyethylene only when the conveyed powder has a minimum ignition energy above 30 mJ and is not classified as a combustible dust. The rotomolded LLDPE cone or hopper section is molded with 5–8 mm walls and a 0.5–1.0 wt% carbon black masterbatch when color coding is required but UV shielding is not. Food-contact dry bulk hoppers are molded to FDA 21 CFR 177.1520 and EU 10/2011 with pre-cleaned mold release; surface silicon levels above 0.2% by XPS cause adhesion failure in downstream elastomer gaskets. The rotomolding process uses a biaxial rotation ratio of 4:1 and a peak internal air temperature of 195–205 °C for 12–18 min; cooling is forced air only to minimize sink distortion across the cone-to-cylinder transition. Dimensional tolerance on the outlet flange is held to ±0.5% of nominal diameter, checked with a calibrated plug gauge after 24 h post-mold shrinkage stabilization. The terminal articles are hopper bodies, discharge cones, and transition chutes from 50 L to 1,000 L, used in pneumatic conveying of granular food ingredients and plastic pellets; they replace stainless steel only where impact abrasion is low and cleanout is performed by dry wipe rather than steam sterilization.
Large rotomolded machine covers and enclosures built with this grade often fail by warpage when cooling is unbalanced across the mold surface. To hold a flat side-panel tolerance of ±0.8 mm over 1,200 mm, the mold is rotated on a carousel machine with a programmed fan delay: after oven removal the mold is held for 4–6 min in still air before forced-air fans at 0.75 m/s are directed at the backside ribs. This profile limits the shell cooling rate to 8–12 °C/min through the recrystallization interval. The powder is blended with 0.3–0.5 wt% color masterbatch and 5% internal regrind when surface appearance permits; gate and insert bosses are reinforced with molded-in brass inserts preheated to 110–120 °C. Heat deflection temperature under 0.45 MPa is measured by ISO 75-2/B at 45–55 °C, so large flat panels require ribbing or steel backing when the service environment exceeds 50 °C. Chemical resistance to 10% quaternary ammonium disinfectant is validated by 24 h immersion per ISO 175 with no visible change and less than 1% mass change. The end products are equipment enclosures, pump housings, and medical cart structural covers where structural foam is not acceptable and chemical resistance to disinfectant wipes is required.
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LyondellBasell Icorene 3560 BUE 5123 is a linear low density polyethylene powder supplied for rotational moulding of hollow goods. The code identifies the Icorene 3560 base resin in combination with a BUE 5123 additive package. The designation is not a numerical specification; density, melt index, sieve cut and additive loading must be read from the batch certificate or the product data sheet. For incoming material, density is measured according to ISO 1183-1:2019 and melt mass-flow index according to ISO 1133-1:2022. The BUE 5123 suffix denotes a UV-stabilised formulation intended for exterior service, but the term UV-stabilised does not replace weathering validation on the final moulded article. Published data for this specific configuration are limited; therefore property limits used for design should be confirmed on each delivery lot rather than assumed from the grade name.
A rotational moulding grade with multiple lot sources may vary in dry flow, bulk density and sieve distribution. The following measurements are performed before release: bulk density per ISO 60:1977, melt mass-flow index at 190 °C under 2.16 kg per ISO 1133-1:2022, density per ISO 1183-1:2019, and sieve distribution per ASTM D1921-18 or ISO 4610:2001. LLDPE rotomoulding powders of this class are generally supplied with a bulk density in the 0.30–0.40 g/cm³ band; values below 0.28 g/cm³ may cause hopper bridging, while excessive fines through a 75 µm sieve contribute to dust and pinhole formation. The melt index of rotational moulding LLDPE is commonly held between 2 and 8 g/10 min; higher melt index accelerates particle coalescence but may reduce environmental stress-crack resistance and low-temperature impact. Density for a butene LLDPE platform is normally in the 0.925–0.940 g/cm³ band, but the specific value for this product must be confirmed against the manufacturer’s batch certificate.
| Measurement | Method | Unit | Operational relevance |
|---|---|---|---|
| Melt mass-flow index | ISO 1133-1:2022 | g/10 min | Controls powder coalescence and oven hold time |
| Density | ISO 1183-1:2019 | g/cm³ | Controls stiffness, shrinkage and ESCR balance |
| Bulk density | ISO 60:1977 | g/cm³ | Controls hopper feed consistency |
| Particle size distribution | ASTM D1921-18 or ISO 4610:2001 | % retained | Controls bubble release and pinholing |
| Tensile yield stress and elongation | ISO 527-2:2012 | MPa, % | Confirms moulded wall ductility after cooling |
| Flexural modulus | ISO 178:2019 | MPa | Compares stiffness with HDPE or MDPE alternatives |
| Charpy notched impact | ISO 179-1:2010 | kJ/m² | Confirms low-temperature impact, especially at -20 °C and -30 °C |
| Environmental stress-crack resistance | ASTM D1693-22 | h | Predicts failure time for tanks and detergent containers |
| Vicat softening point A50 | ISO 306:2022 | °C | Indicates short-term temperature resistance |
| Melting peak | ISO 11357-3:2018 | °C | Used to set peak internal air temperature target |
On shuttle and carousel machines, the critical process window is set not by the mould shell thermocouple but by the internal air temperature. For LLDPE powders, oven chamber temperature is commonly set between 280 °C and 330 °C, while the peak internal air temperature is controlled in the 190 °C to 205 °C band. Internal air temperatures above 215 °C increase thermo-oxidative chain scission, which appears as yellowing, loss of tensile elongation and reduced Charpy impact; temperatures below 185 °C produce incomplete particle fusion and porosity. The hold time at peak internal air temperature is thickness-dependent: a 6 mm wall may require 20–25 min at temperature, while a 12 mm wall may require 35–45 min, but machine-dependent variables such as mould swing diameter, heating intensity and rotation ratio make a single universal cycle invalid. The rotation ratio is commonly set between 3:1 and 5:1 for symmetric parts; complex shells require programmed variable-speed rotation to avoid thinning along the parting line. Sudden water quench after release can reduce warpage but may introduce low-temperature impact loss. Air cooling followed by water mist is used on thin LLDPE shells. Mould shrinkage should be measured on the actual tool and is typically in the 1.5–2.5% range for LLDPE rotomoulding powders. Regrind levels above 15 wt% are common only when impact and ESCR are retested because particle size distribution changes and the UV stabiliser package is diluted.
In relation to other polyethylenes, the base polymer of Icorene 3560 BUE 5123 is a linear low density ethylene copolymer with short-chain branches. It does not have the long-chain branching of LDPE; therefore at equivalent melt index it has higher tensile modulus and tensile strength. Compared with HDPE rotomoulding grades, the LLDPE class has lower density, lower flexural modulus and lower continuous load resistance, but usually better stress-crack resistance and low-temperature impact. An HDPE rotomoulding grade with density near 0.955 g/cm³ may show flexural modulus in the 900–1,100 MPa band, whereas an LLDPE with density near 0.935 g/cm³ often falls in the 250–450 MPa band under ISO 178:2019. This stiffness difference determines wall thickness: an LLDPE tank may require ribbing or a thicker nominal wall to achieve the same deflection limit as an HDPE tank. MDPE occupies the intermediate space, with density in the 0.940–0.950 g/cm³ band and a more balanced stiffness-impact profile. Compared with hexene or metallocene LLDPE, a butene LLDPE tends to have lower dart impact and lower ESCR; however, rotational moulding processability may be more forgiving because powder densification occurs more readily. Selection should be made after comparing ISO 179-1:2010 Charpy impact and ASTM D1693-22 ESCR data, not on density alone. The designation does not indicate a chemically crosslinkable grade; if peroxide or silane crosslinking is required, a different product family should be specified.
For outdoor service, the BUE 5123 stabiliser package is intended to delay UV-induced chain scission and surface craze development in moulded parts. Weathering qualification should be performed on the finished article, not on the powder, using ISO 4892-2:2013 or ISO 4892-3:2016 and evaluating retained tensile elongation per ISO 527-2:2012 or retained Charpy impact per ISO 179-1:2010. A common acceptance benchmark for exterior PE articles is a retained elongation of at least 50% after 3,000 h of accelerated weathering, but published data for this specific BUE 5123 formulation are limited. Darker colourants and mineral pigments such as iron oxide can raise surface temperature and shorten service life; the design should therefore account for thermal ageing at the same time as UV ageing. Chemical resistance should be assessed according to ISO 175:2010. LLDPE is generally resistant to dilute acids and alkalis, but is not recommended for continuous contact with strong oxidising acids, chlorinated solvents, or aromatic hydrocarbons at elevated temperature. Regulatory compliance is article- and use-dependent. For food-contact mouldings, the converter must obtain a supplier declaration and verify the final article under Commission Regulation (EU) No 10/2011 and, where applicable, FDA 21 CFR 177.1520 for olefin polymers; the additive package in BUE 5123 must be covered by the specific migration limits. Under REACH, polyethylene polymers are generally exempt from registration as polymers, but monomers and additives must be registered. Store the powder in closed packaging below 40 °C and below 60% relative humidity; if condensation has occurred, dry at 70–80 °C for 2–4 h before moulding. During processing, avoid melt contact with acetal, polyamide and chlorinated polymers because degradation products may accelerate polyethylene oxidation.