| HS Code | 698728 |
| Density | 0.935 g/cm³ |
| Melt Flow Rate | 3.5 g/10 min |
| Tensile Strength At Yield | 15.2 MPa |
| Tensile Strength At Break | 22.1 MPa |
| Elongation At Break | 800 % |
| Flexural Modulus | 621 MPa |
| Hardness Shore D | 50 |
| Vicat Softening Point | 108 °C |
| Melting Point | 124 °C |
| Thermal Expansion Coefficient | 1.30E-4 1/°C |
| Specific Heat Capacity | 2.30 J/g·°C |
| Dielectric Constant | 2.3 |
| Volume Resistivity | 1.00E+15 ohm·cm |
As an accredited LyondellBasell Icorene 3545 WHB 9619 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 3545 WHB 9619 LLDPE is packaged in 25 kg polyethylene-lined paper bags, 40 bags per pallet (1,000 kg). |
| Container Loading (20′ FCL) | LyondellBasell Icorene 3545 WHB 9619 Linear Low Density Polyethylene loaded in a 20′ FCL container, securely stowed and sealed. |
| Shipping | LyondellBasell Icorene 3545 WHB 9619 Polyethylene, Linear Low Density, is non-hazardous and not DOT/ADR/IMDG regulated. It ships in 25 kg bags, octabins, or bulk trucks/railcars. Keep containers sealed and maintain cool, dry conditions, avoiding excessive heat or sunlight. No UN number or hazardous placards required. |
| Storage | Store LyondellBasell Icorene 3545 WHB 9619 Polyethylene, Linear Low Density in a cool, dry, well-ventilated warehouse. Keep bags/containers closed, palletized, and away from direct sunlight, heat, flames, and strong oxidizers. Prevent moisture, dust, and static buildup. Avoid prolonged UV exposure and excessive temperatures. Follow the SDS and local regulations. |
| Shelf Life | Shelf life is typically 24 months from production when stored unopened in cool, dry conditions, away from sunlight and moisture. |
| Wall thickness (mm) | Oven dwell time (min) | PIAT target (°C) | Air cooling (min) | Water cooling (min) |
|---|---|---|---|---|
| 4.0 | 18–22 | 190–210 | 8–10 | 4–6 |
| 6.0 | 24–28 | 195–215 | 10–14 | 6–8 |
| 8.0 | 30–36 | 200–220 | 14–18 | 8–12 |
| 10.0 | 36–44 | 205–225 | 16–22 | 10–14 |
Parameter windows represent published ranges for LLDPE rotomolding grades in the 0.930–0.938 g/cm³ density class and vary with machine design, mold material, and part geometry. Finished product compliance for potable water contact requires FDA 21 CFR 177.1520(c) olefin polymers clearance, while chemical storage tank applications require validation against UN/DOT 6A packaging specifications when used for hazardous material transport. Mold release systems employ semi-permanent silicone or PTFE-based coatings applied at 2–4 µm dry film thickness; incompatibility exists with certain migrating slip additives that cause delamination of the mold coating and surface defects on the molded part. Terminal product categories include: rotationally molded cylindrical and rectangular water storage tanks (500–20000 L capacity), double-wall chemical storage tanks with secondary containment per EN 13575:2012, kayak hulls and recreational craft hulls, agricultural feed silos, and industrial material handling bins.
Shrinkage behavior in injection-molded LLDPE thin-wall containers is dominated by the interaction between flow-induced molecular orientation and crystallization kinetics under non-isothermal mold cooling. When the melt enters a mold cavity at temperatures between 190°C and 240°C, directional shear imparts orientation to the polymer chains along the flow path; subsequent rapid crystallization against a mold wall held at 15–40°C freezes this oriented structure before stress relaxation can occur. The resulting differential shrinkage—typically 1.5–2.5% in the flow direction and 1.0–1.5% in the transverse direction as determined by ISO 294-4:2018 on standardized 60 mm × 60 mm × 2 mm plaques—causes warpage in flat-bottomed containers with aspect ratios exceeding 3:1. Machine-specific variables include injection velocity profiles, holding pressure (typically 300–600 bar), and gate geometry. A gate diameter below 1.5 mm generates excessive shear heating at flow front velocities exceeding 300 mm/s, resulting in localized material degradation at the gate vestige. Tooling temperature control via manifold water circuits permitted under ISO 16928 mold cooling design practice maintains a temperature differential of less than ±3°C across the cavity surface to minimize asymmetric cooling. Addition levels for this application typically employ the resin at 100% by weight for food-contact housewares, or blended with HDPE at 20–40 wt% HDPE to increase flexural modulus by approximately 150–300 MPa for industrial container applications. The flexural modulus of LLDPE in this density range typically falls between 450 MPa and 700 MPa (ASTM D790, Method I). Compliance for food contact applications requires FDA 21 CFR 177.1520(c) Table 2 certification, EU Regulation (EU) No 10/2011 with overall migration limits of 10 mg/dm², and REACH registration confirmation. Terminal product categories include: household storage containers with living-hinge lids, thin-wall buckets (0.5–10 L capacity) for paint and food packaging, toy components tested to EN 71-3 migration of certain elements, and industrial pails. Operational boundaries include pre-drying at 80°C for 2–4 hours when ambient relative humidity exceeds 60%, as absorbed moisture causes surface splay and mechanical property degradation. The combination with certain halogenated flame retardant additives is to be avoided at processing temperatures above 230°C due to dehydrohalogenation and subsequent autocatalytic polymer degradation.
Blown film extrusion of LLDPE resin in this density range operates with fundamentally different bubble dynamics than LDPE systems, particularly regarding bubble stability and frost-line positioning. The low melt strength of LLDPE relative to LDPE necessitates a die gap of 1.5–2.5 mm (versus 0.8–1.2 mm for LDPE) to prevent melt fracture from excessive shear stress at the die lip. Blow-up ratios (BUR) between 2.0:1 and 3.5:1 are obtainable on production-scale lines with internal bubble cooling (IBC) systems, whereas without IBC, the upper BUR limit typically falls to 2.5:1 due to bubble instability. The frost-line height for LLDPE films typically stabilizes at 3–6 die diameters above the die face under processing conditions of 200–220°C melt temperature and 15–25°C ambient cooling air. Unlike LDPE, whose broad molecular weight distribution permits stable bubble formation at high take-up speeds without internal cooling, LLDPE films require careful control of internal air pressure to prevent bubble flutter that generates gauge variation exceeding ±8% across the web width. Machine direction (MD) and transverse direction (TD) tensile properties for LLDPE films conform to ASTM D882; values for film grades in this density class exceed 45 MPa MD and 40 MPa TD tensile strength with elongation at break values exceeding 600% in both directions. Formulation practice commonly blends the resin with LDPE at 20–50 wt% LLDPE loading to improve mechanical toughness while maintaining bubble stability; addition levels above 50 wt% LLDPE require extruder modifications including increased die gap, raised motor torque capacity, and IBC installation. Extruder specifications for LLDPE film processing include single-screw designs with L/D of 24:1 to 30:1, compression ratio 2.5:1 to 3.5:1, and barrel zone temperature profiling from 160°C at the feed throat to 210°C at the adapter. Melt pressure at the die entry is to remain below 350 bar to prevent excessive shear heating. Compliance standards applicable to film applications include FDA 21 CFR 177.1520 for food packaging, EU Regulation (EC) No 1935/2004 for food contact materials, and ISO 527-3 for tensile property determination on films less than 1 mm thick. Terminal product categories include: agricultural silage stretch film (25–75 µm thickness), heavy-duty shipping sacks, linear low-density geomembranes, collation shrink overwrap, and freezer-grade food packaging film. The incompatibility of pure LLDPE formulations with certain anti-blocking agents that migrate to the film surface and interfere with corona surface treatment (target surface energy 38–42 dynes/cm) used for print adhesion is documented in production trials.
Typically, LLDPE carrier resins in filled compound manufacture operate at filler loadings between 60 wt% and 80 wt% calcium carbonate or talc on co-rotating twin-screw extruders with L/D of 40:1 to 52:1. The resin functions as the thermoplastic matrix that wets filler particles and transfers shear stress during mixing; specific energy input ranges from 0.15 kWh/kg to 0.25 kWh/kg depending on filler type and moisture content. Barrel temperature profiling follows a descending gradient from 220°C in the feed zone to 180°C at the die to maintain melt viscosity sufficient for filler dispersion while preventing thermal degradation. Torque rheometry characterization per ISO 20965-1 provides mixing energy curves used to determine the maximum filler loading achievable before melt viscosity exceeds the torque capacity of the extruder drive system—an upper bound of 25 N·m for laboratory-scale instruments is common. Melt flow rate testing per ISO 1133-1:2022 at 190°C/2.16 kg load provides quality control verification of batch-to-batch consistency; MFR values for filled compounds in this class fall between 0.5 g/10 min and 3 g/10 min depending on filler loading. Dispersion quality is assessed by filter pressure value testing per EN 13900-5 for pigment concentrate applications. Terminal product categories include: color masterbatch pellets for downstream polyolefin processors, calcium carbonate-filled compounds for extrusion of sheets and films, and talc-filled compounds for injection-molded automotive interior components (when talc purity exceeds 95% and complies with ISO 3451 ash content limits).
| Application segment | Food contact | Mechanical testing | Application-specific |
|---|---|---|---|
| Rotational molding | FDA 21 CFR 177.1520(c) | ASTM D1693, ASTM D638 | EN 13575:2012 |
| Injection molding | EU Reg. 10/2011 | ISO 294-4:2018 | EN 71-3 |
| Blown film | EU 1935/2004 | ASTM D882 | ISO 527-3 |
| Compounding | — | ISO 1133-1:2022 | EN 13900-5 |
| Pipe extrusion | — | ISO 4427-2:2019 | ASTM D3350, ASTM D2837 |
| Wire & cable | — | IEC 60811-100 | UL 1581, ASTM D1248 |
Single-screw extrusion of LLDPE for pipe and conduit applications requires barrel temperature profiles that differ measurably from those used for HDPE of equivalent melt viscosity. A single-screw extruder with L/D of 30:1 and compression ratio of 3:1 configured with a grooved feed section establishes conveying capacity at the feed throat; barrel zone temperatures are set from 160°C at the feed section to 200–210°C at the metering zone and 220°C at the adapter flange. Melt pressure upstream of the screen pack should not exceed 300 bar to prevent excessive shear heating and subsequent degradation; screen packs are typically configured with 40/60/80 mesh progressive filtration elements. Die design for LLDPE conduit employs a draw-down ratio (DDR) between 2:1 and 4:1 and a draw balance that accommodates the higher die swell of LLDPE relative to HDPE—die swell values of 15–20% versus 10–12% for HDPE. Vacuum calibration tank sizing produces outside diameter tolerances of ±0.15 mm for conduit diameters up to 50 mm; cooling water temperature is maintained at 15–25°C with a cooling tank length sufficient to lower pipe surface temperature below 70°C before puller contact. Formulation in conduit applications may include 2–3 wt% carbon black for UV stabilization per ISO 6964; incorporation method uses masterbatch dosing at the extruder throat with a gravimetric feeder to achieve dispersion quality assessed by particle count per ISO 18553. Pipe extrusion compliance for pressure-rated water service requires classification per ASTM D3350 cell classification system and ISO 4427-2:2019 for PE water supply pipes; protective electrical conduit must meet UL 651 Schedule 40 and Schedule 80 requirements. Terminal product categories include: non-pressure drainage pipes, corrugated protective conduit for underground electrical cabling, water service lateral pipes, and telecommunications ducting. Published data specific to the WHB 9619 additive configuration in pipe applications is limited; hydrostatic design basis (HDB) values derived from ASTM D2837 long-term testing should be confirmed from the supplier's technical data sheet before specifying for pressure-rated applications.
Wire and cable jacketing extrusion runs with LLDPE base resin demand different processing windows than conventional LDPE grades due to higher melt viscosity and lower shear sensitivity. On single-screw extruders with L/D of 24:1 to 30:1 and a compression ratio of 3:1, the melt temperature is maintained between 190°C and 220°C at the head, with die pressure limited to 250 bar to prevent melt fracture at the cable jacket surface. Pressure-type die designs with a die land length-to-gap ratio exceeding 10:1 minimize surface roughness on jacketed cables. The higher viscosity of LLDPE relative to LDPE at equivalent melt index means barrel zone temperatures in the metering section are typically 10–20°C higher to achieve equivalent throughput. Jacketing wall thicknesses range from 0.5 mm to 3.0 mm depending on conductor diameter and voltage class; concentricity is maintained to ±0.05 mm via closed-loop die centering systems. The cable cooling trough operates at water temperatures of 15–25°C, and a cooling length of 20–40 m is required for medium-speed lines running at 50–150 m/min. Compliance standards applicable to polyolefin insulation include IEC 60811-100 for mechanical test methods on insulating and sheathing materials, ASTM D1248-12 for polyethylene plastic extrusion materials for wire and cable, and UL 1581 reference Standard for Electrical Wires, Cables, and Flexible Cords. Flame retardant requirements in jacketing formulations often necessitate halogen-free additives; the incompatibility of certain intumescent flame retardant systems with LLDPE matrices leads to significant reductions in elongation at break—data generated on filled systems shows elongation falling from an unfilled value exceeding 800% (ASTM D638) to below 200% at 30 wt% additive loading. Terminal product categories include: low-voltage building wire insulation (600 V rating), telecommunications cable jackets, and portable power cable sheathing.
Competitive LyondellBasell Icorene 3545 WHB 9619 Polyethylene, Linear Low Density prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please contact us at +8618005193850 or mail to sales8@ascent-chem.com.
We will respond to you as soon as possible.
Tel: +8618005193850
Email: sales8@ascent-chem.com
Flexible payment, competitive price, premium service - Inquire now!
LyondellBasell Icorene 3545 WHB 9619 is classified as a linear low-density polyethylene rotational moulding powder. The base polymer is commonly characterized by a density of 0.934 g/cm³ when tested under ISO 1183-1 or ASTM D1505, and a melt flow rate of 4.0 g/10 min under ISO 1133-1 or ASTM D1238 at 190 °C with 2.16 kg load. The suffix WHB 9619 may identify packaging, colour, or additive batch information; it should not be treated as an alternate polymer architecture marker without the certificate of analysis. In practice, the powder is charged into closed moulds on carousel, shuttle, or rock-and-roll rotational moulding machines. The principal end uses are hollow parts requiring a balance of low-temperature impact resistance, environmental stress crack resistance, and moderate flexural stiffness: agricultural spray tanks, general-purpose storage vessels, recreational components, and industrial covers.
Against a 0.945 g/cm³ high-density polyethylene rotomoulding grade, the lower density of Icorene 3545 reduces crystallinity and flexural modulus but improves environmental stress crack resistance and sub-ambient impact performance. The trade-off is measurable: a part designed for an HDPE grade at a flexural modulus near 800 MPa cannot typically be substituted at equal wall thickness without increased deflection under load. Compared with film-grade LLDPE, this product is milled to a controlled rotomoulding sieve fraction and carries a stabilizer package intended for long oven residence times and low-shear rotational moulding rather than high-shear blown film extrusion. Against high-flow LLDPE injection moulding grades, the 4.0 g/10 min melt flow rate is low enough to retain melt strength during the slow coalescence stage, reducing the potential for uneven thinning on vertical walls. If comparison is made to metallocene LLDPE rotomoulding powders, molecular weight distribution, plateau modulus, and shear response may differ even when density and melt flow rate appear similar. The manufacturer’s catalyst and molecular architecture data should be requested before direct substitution.
On production-scale carousel machines, oven air temperature and peak internal air temperature are independent variables. Oven set points between 260 °C and 320 °C are common for LLDPE rotomoulding powders, but the material reaches a fully sintered condition only when the internal air temperature plateaus in the range of 190–210 °C. The arm speed is set to produce a tumbling powder bed; typical primary-axis speeds are 4–8 rpm, with secondary-axis speeds near 1–2 rpm, depending on part diameter and the ratio of the two axes. In forced-air ovens, an air velocity of 3–5 m/s across the mould surface increases the heat transfer coefficient and can shorten the cycle, but uneven airflow across a multi-arm carousel can shift the peak internal air temperature by more than 5 °C between arms. That degree of shift may not appear as a gross defect; however, impact and stress crack tests can expose the difference.
The conflict arises because the sintering plateau for LLDPE is narrow. A reduction of 5 °C in peak internal air temperature can leave the inner-wall surface partially sintered without forming a visible pinhole, but the residual porosity acts as an initiation site for slow crack growth. Standard control therefore uses internal air thermocouples or contact thermocouples embedded in the mould wall, with the temperature trace recorded for each arm cycle. The acceptable peak internal air temperature band is often maintained at ±3 °C around the target. Raising peak internal air temperature above the oxidative threshold increases carbonyl concentration and shifts colour; yellowness can be tracked under ASTM E313 and elongation retention under ASTM D638. In a covered tank or fuel container, an oxidized inner surface may increase the risk of stress cracking in contact with surfactants, detergents, or organic liquids. The exact peak internal air temperature target depends on wall thickness, mould thermal conductivity, and internal air velocity profile; no single oven temperature should be applied across all tools.
Before the thermal cycle is fixed, the incoming powder should be characterized for bulk density and sieve fraction. A low bulk density reduces the charge weight for a given mould volume and can produce a thin-wall condition; a bulk density below 0.48 g/cm³ under ASTM D1895 should trigger a sieve analysis. Excessive coarse material above 500 µm (35 mesh) can create surface pits, while excessive fines below 125 µm can segregate during rotation and cause gloss variation on the inner surface. Calibration of the milled powder is checked under ASTM D1921. Polyethylene is not hygroscopic, but condensation from cold storage should be avoided because surface moisture can produce steam bubbles at the mould wall. The powder should be stored in sealed containers at temperatures below 50 °C, away from direct sunlight and strong oxidizing agents.
The following envelope is representative of a rotational moulding LLDPE in the 0.934 g/cm³ and 4.0 g/10 min class. It is a screening matrix, not a certificate of analysis.
| Characteristic | Test method | Representative range | Relevance to use |
|---|---|---|---|
| Density | ISO 1183-1 / ASTM D1505 | 0.932–0.936 g/cm³ | Controls stiffness, chemical resistance, sink/float behaviour |
| Melt flow rate | ISO 1133-1 / ASTM D1238 at 190 °C/2.16 kg | 3.8–4.2 g/10 min | Powder coalescence and melt distribution |
| Tensile yield strength | ISO 527-2 / ASTM D638 | 14–18 MPa | Structural design of hollow parts |
| Elongation at break | ISO 527-2 / ASTM D638 | 600–900% | Ductility before fracture |
| Flexural modulus | ISO 178 / ASTM D790 | 350–450 MPa | Load deflection under bending |
| Environmental stress crack resistance | ASTM D1693 Condition B, 100% Igepal | >1,000 h | Stress crack resistance in detergent/chemical environments |
| Vicat softening point | ISO 306/A50 / ASTM D1525 | 110–118 °C | Temperature resistance limit |
| Low-temperature brittleness | ASTM D746 / ISO 974 | < -76 °C | Sub-zero impact safety |
For the exact Icorene 3545 WHB 9619 lot, the manufacturer’s certificate is controlling; if the suffix designates a white or colour-concentrate version, density, melt flow rate, and additive-related properties may depart slightly from the base-resin envelope.
Food-contact and drinking-water approvals are not automatic. The base olefin polymer is typically evaluated against FDA 21 CFR 177.1520 in the United States and Regulation (EU) No 10/2011 in the European Union, but finished-article compliance depends on the complete recipe, including internal mould release agents, dry-flow additives, and colour concentrates. The overall migration limit of 10 mg/dm² under EU 10/2011 must be verified on the final article, not on the powder alone. For heavy metals and restricted substances, REACH 1907/2006 and RoHS 2011/65/EU apply at the article level. End users should obtain a written formulation disclosure from the converter and the resin supplier when the part is intended for potable water or food-contact service.
Outdoor weathering is not an inherent property of the base resin. If the suffix WHB 9619 denotes a white or natural grade, ultraviolet resistance will be limited unless a stabilizer additive is present. Black LLDPE rotomoulding formulations often use carbon black at 2–3 wt%, but black pigment alone does not guarantee weather resistance; the hindered amine stabilizer package must be validated by ISO 4892-2 or ASTM G155 exposure and retained impact/tensile testing. In agricultural tanks, chemical compatibility with fertilizers, alcohols, and surfactant-based cleaning agents should be tested under ASTM D1693 and, where appropriate, ISO 16770 notched constant tensile load at the maximum service temperature.
LLDPE rotomoulded parts exhibit post-mould shrinkage that can vary between 2% and 3% depending on wall thickness, cooling rate, and pigmentation. Demoulding above 80–90 °C can increase distortion because the part retains insufficient modulus to resist gravitational and clamping forces. Forced-air cooling is preferred initially, followed by water mist if faster cycles are required; immediate water quenching can create a gradient between the outer and inner skins and lock in residual stress. Dimensional checks should be made after conditioning at 23 ±2 °C and 50 ±5% relative humidity for not less than 24 h under ISO 291 or ASTM D618. The same conditioning applies before mechanical testing, because polyethylene properties are temperature- and rate-sensitive.
The operational limits below summarize typical start-up and troubleshooting points for this product class. Actual cycle optimization must be performed on the specific mould.
| Processing variable | Typical band | Measurement / control method | Failure mode outside band |
|---|---|---|---|
| Oven air temperature | 260–320 °C | Oven thermocouple / air temperature recorder | Low: incomplete sintering; high: surface oxidation, yellowing |
| Peak internal air temperature | 190–210 °C | Internal air thermocouple or mould-wall data logger | Low: pinholes, loss of ESCR; high: blowholes, odour, brittleness |
| Powder bulk density | ≥0.48 g/cm³ | ASTM D1895 | Below band: thin walls, poor charge weight |
| Sieve fraction upper limit | 500 µm (35 mesh), fines <125 µm controlled | ASTM D1921 | Coarse: surface pits, poor coalescence; fines: segregation, gloss variation |
| Mould release temperature | <80 °C | Infrared pyrometer / contact thermocouple | Higher: warpage, shrinkage anisotropy |
| Primary axis rotation speed | 4–8 rpm | Tachometer on arm | Too low: powder pooling; too high: centrifugal thinning |
Regrind addition from rejected parts changes the powder bed. Sieved regrind should be blended at controlled percentages because the particle shape is more angular and the bulk density may differ from virgin powder. A secondary milling step is often required to maintain 35 mesh upper particle size. The proportion of regrind should be limited and recorded; additions above 30 wt% may reduce impact performance and require revalidation of ASTM D1693 environmental stress crack resistance. The same caution applies to dry-blended colorants and flow additives: only additives with known decomposition temperatures above the oven set point should be used.
In chemical service, this polymer is not suitable for continuous contact with strong oxidizing acids, halogens, or low-boiling aromatic and chlorinated solvents at elevated temperatures. Environmental stress-cracking agents include silicone oils, certain surfactant solutions, and glycol-based heat-transfer fluids; each candidate fluid should be tested in the actual liquid at the maximum service temperature using ASTM D1693 or ISO 16770. Melt processing in continuous contact with copper or copper-alloy surfaces should be avoided because copper ions can accelerate oxidative degradation. These limitations are not unique to Icorene 3545 but are necessary for reliable service life estimates.
Incoming lot acceptance should include melt flow rate, density, bulk density, and sieve analysis. On a production carousel, three lots should be moulded using the same tool and temperature trace, and cut specimens from identical positions should be compared for ASTM D638 tensile elongation and ISO 6603-2 impact energy. This is required because a batch-to-batch melt flow rate shift of ±0.2 g/10 min or a bulk density change can move the effective peak internal air temperature by several degrees. Such shifts may not be visible until parts are subjected to stress cracking or sub-zero impact tests.