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Borealis Queo VLDPE 8230

    VTB
    Specifications
    HS Code 417312
    Density 0.882 g/cm³
    Melt Flow Rate 190 C 2 16 Kg 3.0 g/10 min
    Melting Temperature 70 °C
    Vicat Softening Temperature 45 °C
    Tensile Modulus 65 MPa
    Flexural Modulus 65 MPa
    Tensile Stress At Break 20 MPa
    Tensile Strain At Break 800 %
    Shore A Hardness 88
    Shore D Hardness 30

    As an accredited Borealis Queo VLDPE 8230 factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Borealis Queo VLDPE 8230 is packaged in 25 kg polyethylene-lined paper bags, with 40 bags per 1,000 kg pallet.
    Container Loading (20′ FCL) Chemical Borealis Queo VLDPE 8230 is palletized and securely loaded in a 20-foot FCL container for ocean transport.
    Shipping **Shipping description:** BOREALIS QUEO VLDPE 8230; solid ethylene copolymer/very low density polyethylene; non-hazardous, not regulated for transport (ADR/RID/IMDG/IATA); no UN number, hazard class, or packing group. Ship in original sealed bags/octabins; keep dry and protected from sunlight and contamination.
    Storage Store Borealis Queo VLDPE 8230 in a cool, dry, well-ventilated area away from direct sunlight, heat, flames, and strong oxidizers. Keep bags or containers closed to prevent moisture, dirt, and contamination. Avoid prolonged high temperatures and static buildup; handle according to the safety data sheet and local regulations.
    Shelf Life Borealis Queo VLDPE 8230 typically has a 24-month shelf life from production when stored dry, cool, and protected from UV.
    Application of Borealis Queo VLDPE 8230
    Hot-melt adhesive compounding for packaging and hygiene lines utilises Queo VLDPE 8230 as a high-flow polyolefin backbone when formulations require low melt viscosity, reduced low-temperature embrittlement, and broad compatibility with hydrogenated tackifier resins. The grade carries a nominal density of 0.882 g/cm³ under ISO 1183-1 and a melt flow rate of 30 g/10 min under ISO 1133-1:2022 at 190 °C/2.16 kg. Its melting peak, determined by differential scanning calorimetry according to ISO 11357-3, lies near 60 °C, which places the practical melt pool temperature in a window of 140 °C to 160 °C. Formulation work for packaging adhesives typically evaluates the plastomer at 10 wt% to 30 wt% of the compound, combined with fully hydrogenated DCPD or C5/C9 tackifier resins at 50–65 wt%, Fischer–Tropsch or polyethylene wax at 5–15 wt%, and hindered phenolic antioxidant at 0.1–0.5 wt%. The low crystallinity of the ethylene-1-octene copolymer delays wax crystallisation during cooling, extending open time on paperboard and corrugated substrates. Adhesion to corona-treated biaxially oriented polypropylene is evaluated by T-peel at 300 mm/min according to ASTM D1876, while shear adhesion failure temperature is measured by ASTM D4498 on a 25 mm × 25 mm overlap shear specimen with 500 g static load. The substitution of EVA with a metallocene VLDPE reduces migration of low-molecular-weight wax fractions and improves low-temperature bond retention, but the nonpolar character of the grade limits wetting on untreated PET and aluminium foil. Production-scale mixing in jacketed sigma-blade kneaders or continuous twin-screw extruders with L/D of at least 32:1 should maintain melt residence time below 40 min under nitrogen blanketing of 1–2 vol% O₂ or lower to avoid yellowing and melt flow drift. End-use formats include case and carton sealing, wrap-around labelling, window patching of paperboard, and pad attachment in disposable hygiene articles. The operational boundary is defined by tackifier–wax phase equilibria: above 68 wt% tackifier, cohesive strength declines and failure mode shifts from peel to stringing, while wax above 18 wt% shortens open time below the requirement for large-panel assembly. In food contact packaging, the formulated adhesive must comply with 21 CFR 175.105 for adhesive components, and the polyolefin backbone falls under the olefin polymer provisions of 21 CFR 177.1520 when used in food-contact layers, with migration limits assessed under 21 CFR 176.170(c) for fatty-food conditions.

    How Does a 30 g/10 min VLDPE Shift the Ductile–Brittle Transition in Polypropylene Impact Compounds?

    Polypropylene homopolymer and mineral-filled polypropylene compounds formulated with 10–30 wt% Queo VLDPE 8230 exhibit a shift from crack-driven brittle fracture to shear-yield-dominated deformation. The plastomer, with density 0.882 g/cm³, introduces a low-crystallinity phase that reduces the brittle failure contribution of the matrix and increases multiple craze initiation under impact loading. In a co-rotating twin-screw extruder with L/D 40:1, the grade is fed into the main hopper together with PP powder so that its low melting point near 60 °C permits early melting and dispersion into domains controlled by the viscosity ratio between the plastomer and the PP matrix at 190 °C to 220 °C. Screw speeds above 300 min⁻¹ and melt temperatures of 180–200 °C reduce domain size, but excessive shear can degrade the low-viscosity VLDPE phase and produce surface haze in injection-molded parts. The resulting compounds are tested for notched Charpy impact strength at 23 °C and -20 °C under ISO 179-1/1eA, while tensile yield stress and elongation at break are measured per ISO 527-2. Flexural modulus is recorded per ISO 178 because the addition of 15 wt% VLDPE improves low-temperature Charpy impact but reduces stiffness; every compound must therefore be balanced against the minimum flexural modulus on the engineering drawing. Automotive interior applications impose additional requirements: fogging behaviour per DIN 75201, odour per VDA 270, and VOC emission per VDA 277 become critical because the metallocene copolymer introduces low-molecular-weight fractions that must be controlled through degassing and stabiliser selection. The grade should not be used above 35 wt% in mineral-filled PP unless co-continuous morphology is intentionally required for high-elongation compounds, because the modulus drop under ISO 178 can fall below the values expected for talc-reinforced PP. Molding operators also observe lower melt temperature requirements and longer gate seal time compared with unfilled PP; injection speed and holding pressure profiles must be adjusted because the modified compound has slower crystallisation and reduced post-mold shrinkage anisotropy measured by ISO 294-4. The processing conflict is the trade-off between impact modification and heat deflection: at loadings above 25 wt%, the Vicat softening temperature measured by ISO 306 can drop below 70 °C in unfilled PP, limiting under-hood applications unless the part is redesigned with heat shields.Masterbatch production for polyolefin films and injection moulding uses carrier resins whose melt viscosity at compounding shear rates determines pigment wetting and dispersion. Queo VLDPE 8230, with its 30 g/10 min melt flow rate under ISO 1133-1:2022 and an ethylene-1-octene backbone, acts as a wetting carrier for furnace black and organic pigments. Carbon black masterbatches with 40–50 wt% pigment, 5–10 wt% PE wax dispersant, and 0.2–0.5 wt% calcium stearate are processed on a co-rotating twin-screw extruder with L/D 36:1. Barrel set temperatures from 120 °C at the feed zone to 180 °C at the die suffice because the carrier melts before full pigment compaction develops. Screw speeds of 250–400 min⁻¹ generate shear rates that wet the pigment surface earlier than a conventional LDPE carrier with a melt flow rate below 8 g/10 min. Pressure drop across a melt filter is monitored according to ISO 13949:2021 to confirm dispersion stability at let-down ratios from 1 wt% to 4 wt%. Film-grade let-down tests include filter pressure value and retained elongation at break under ISO 527-3, while injection-molded articles are checked for surface specks and colour strength by spectrophotometry. The carrier contributes less crystalline haze than LDPE, but it also lowers the Vicat softening temperature of the final part; therefore caps, crates, and technical mouldings must be validated for stackability and warehouse load performance under ISO 306. For toy and packaging applications, the selected masterbatch pigments and additives must satisfy EN 71-3 migration limits and the specific migration limits of Regulation (EU) No 10/2011 when the final article contacts food. Silo storage under nitrogen purge and pellet drying at 60 °C for 2 h prevent moisture-induced feeding fluctuations when the masterbatch is produced in humid climate. The practical limitation is that the grade is not a universal carrier for high-melting engineering polymers such as polyamide or PET, because processing temperatures above 250 °C exceed the thermal stability range of the VLDPE.

    When a Low-Density Plastomer Enters Halogen-Free Flame-Retardant Cable Compounds

    EVA-based halogen-free flame-retardant cable sheathing compounds incorporate 10–20 wt% Queo VLDPE 8230 to compensate the stiffening effect of aluminium trihydroxide and magnesium dihydroxide loadings at 150–200 phr. The grade lowers the low-temperature embrittlement point and restores melt elasticity during pressure extrusion of cable jackets. In a Buss co-kneader or a twin-screw extruder with L/D 32:1, the plastomer is added with the EVA and flame-retardant filler so that its low melting peak near 60 °C contributes to early fluxing. Processing barrel temperatures are held between 150 °C and 190 °C; exceeding 200 °C risks dehydration of magnesium hydroxide and accelerated acid-catalysed degradation of the polymer matrix. The hydrated fillers require pre-drying at 70–80 °C for 4–6 h before compounding when packaging cannot guarantee moisture levels below 0.05 wt%. Flame retardancy is evaluated by limiting oxygen index according to ISO 4589-2, vertical flame spread according to IEC 60332-1-2, and halogen gas evolution by IEC 60754-1/-2 to confirm that the system remains halogen-free. Low-temperature properties are tested by cold bend and elongation at -40 °C per IEC 60811-504. Because the addition of VLDPE modifies cone calorimeter heat release rate, power and data cable formulations must also be checked under IEC 60332-3 for bunched cable flame propagation if used in building shafts. For global material compliance, the compound should meet the heavy metal restrictions of RoHS Directive 2011/65/EU and be screened against the REACH candidate list for SVHC. The operational limit is clear: the grade replaces rubber flexibilisers but cannot maintain abrasion resistance and hot-set performance above 90 °C in silicone-free formulations unless a crosslinked matrix is introduced through silane grafting or peroxide cure.
    Application areaStandard or regulationTest method or clauseMeasured parameter
    Hot-melt packaging adhesive21 CFR 175.105Adhesive componentsFormulation compliance and migration
    Polyolefin food-contact layer21 CFR 177.1520Olefin polymersFood-contact status and extractives
    PP impact compoundISO 179-1/1eANotched Charpy at 23 °C and -20 °CImpact strength and failure mode
    HFFR cable compoundIEC 60754-1/-2Halogen gas emissionHalogen content and gas corrosivity
    HFFR cable flame spreadIEC 60332-1-2Vertical flame propagationChar height and flaming time
    HFFR low-temperature flexibilityIEC 60811-504Cold bend at -40 °CPass/fail cracking threshold
    Colour masterbatchISO 13949:2021Filter pressure valuePigment dispersion stability
    Stretch filmISO 7765-1Dart drop impactF50 impact mass

    Melt Curtain Stability, Neck-In, and Heat-Seal Initiation in Extrusion Coating

    Extrusion coating lines running LDPE at line speeds above 300 m/min can incorporate 10–30 wt% Queo VLDPE 8230 in the coating blend to initiate heat seals below 100 °C on oriented polypropylene and PET webs. The low-density ethylene-1-octene copolymer reduces seal initiation temperature when compared with LDPE, but it increases neck-in and weakens the melt curtain if added beyond 30 wt%. On a single-screw extruder with L/D 30:1, melt temperature at the die adapter is held from 230 °C to 280 °C; the low-melting component reduces effective melt viscosity and can cause draw resonance under heavy air-gap stretching. Adhesion to aluminium foil and PET is measured by laminate bond strength according to ASTM F88/F88M after sealing at defined temperature, dwell, and pressure. Heat-seal peel curves are generated according to ASTM F2029 to determine the minimum seal temperature at a 4 N/15 mm threshold. Final structures for snack wrappers, lidding films, and sachet laminates must meet food-contact requirements under 21 CFR 177.1520 for the polyolefin component and Regulation (EU) No 10/2011 for overall migration into simulants. On high-speed lines, the melt curtain is widened by adding high-pressure LDPE; line trials quantify neck-in as the difference between die width and web width at the chill roll nip. Chill roll temperature is maintained at 15–20 °C to solidify the low-modulus coating without blocking. Because the grade contains no slip or antiblock package, winding tensions must be reduced compared with standard LDPE coatings to prevent blocking in the finished roll. Published industrial data on extreme high-line-speed configurations above 400 m/min remain limited; trial runs are recommended to establish a safe operating window for each die gap and coating weight.Cast stretch film lines exploit the low crystallinity and narrow composition distribution of Queo VLDPE 8230 when blended with linear low density polyethylene at 10–25 wt% to reduce the film elastic modulus and improve dart impact and puncture propagation resistance. In a three-layer cast film die, the grade is typically allocated to the core or cling layer rather than the outer skin to control blocking. Processing is performed on a single-screw extruder with screw L/D 30:1 or higher, barrel temperature profile from 160 °C to 210 °C, and a chill roll temperature of 18–24 °C. The film is tested for tensile properties in the machine and transverse directions per ISO 527-3, dart drop impact per ISO 7765-1, and puncture resistance per ASTM D5748. For pallet-wrap service, the film must maintain stretch force retention after 200 % pre-stretch on a power stretch wrapper; load retention is evaluated by on-pallet creep tests rather than a single material standard. The addition of VLDPE reduces roll telescoping caused by uneven stress relaxation but may require a higher concentration of polyisobutylene or low-density polyolefin tackifier in the cling layer. Food-contact compliance for poultry and produce wrapping is established under 21 CFR 177.1520, while industrial stretch film is not subject to food-contact migration but must still meet REACH registration obligations for the imported compound. A practical limitation is the reduction in machine-direction tear resistance; film converters compensate by adjusting frost line height or using a skin layer with 5–10 wt% HDPE.
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