| HS Code | 219589 |
| Productname | Mitsui Chemicals TAFMER VLDPE DF710 |
| Manufacturer | Mitsui Chemicals |
| Grade | DF710 |
| Materialtype | Very Low Density Polyethylene (VLDPE) |
| Polymertype | Ethylene-Butene Copolymer |
| Comonomer | 1-Butene |
| Density | 0.908 g/cm3 |
| Meltflowrate | 1.2 g/10 min (190°C, 2.16 kg) |
| Meltingpoint | 75°C |
| Vicatsofteningpoint | 58°C |
| Shoreahardness | 88 |
| Shoredhardness | 28 |
| Tensilestrengthatbreak | 15 MPa |
| Elongationatbreak | >800% |
| Flexuralmodulus | 50 MPa |
| Brittlenesstemperature | < -70°C |
As an accredited Mitsui Chemicals TAFMER VLDPE DF710 factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Mitsui Chemicals TAFMER VLDPE DF710 packaging: 25 kg moisture-resistant paper bags, stacked and palletized for secure industrial shipment. |
| Container Loading (20′ FCL) | 20′ FCL loaded with 25 kg bags of Mitsui Chemicals TAFMER VLDPE DF710, palletized, shrink-wrapped, and secured for ocean transport. |
| Shipping | Mitsui Chemicals TAFMER VLDPE DF710 is shipped as non-hazardous thermoplastic pellets, typically in moisture-barrier 25 kg bags on pallets. Transport and store in a cool, dry, ventilated area away from direct sunlight, moisture, and contamination. No special dangerous-goods classification applies. |
| Storage | Store Mitsui Chemicals TAFMER VLDPE DF710 in a cool, dry, well-ventilated warehouse away from direct sunlight, heat, flames, and strong oxidizing agents. Keep bags/containers closed, clean, and palletized to prevent moisture and contamination. Avoid prolonged high temperatures, UV exposure, and excessive stacking; use good housekeeping and follow the manufacturer’s SDS for safe handling and shelf life. |
| Shelf Life | Shelf life is generally 24 months from production date when stored in original unopened packaging under cool, dry conditions. |
In cast-film and blown-film coextrusion, a sealant layer containing TAFMER DF710 in the range of 70–100 wt% with a linear low-density polyethylene diluent at 0–30 wt% is deposited onto oriented PET or metallised OPP. The resin’s published density of 0.870 g/cm³ per ISO 1183-1:2019 and melt flow rate of 1.2 g/10 min at 190 °C/2.16 kg per ISO 1133-1:2022 place it at the lower-viscosity end of sealant-layer materials, which reduces transverse thickness variation on flat dies when melt temperature at the die lip is maintained at 220–240 °C. The melting peak near 55 °C permits seal initiation on form-fill-seal lines at lower jaw temperatures than PP copolymers, but the same low crystallinity creates a permanent blocking risk in wound rolls. Chill-roll temperature is therefore set at 18–25 °C, and winding tension is held below 0.35 N/mm for a 25 µm web to limit roll hardness and avoid interlayer adhesion. Air-knife pinning systems must not supply air above 30 °C; warmer air softens the web before quenching and causes edge necking, while air below 15 °C can introduce condensation. In lamination, the sealant layer is activated by a heated jaw or ultrasonic horn, and seal strength is measured per ASTM F88/F88M-21 on a universal tensile tester; target values are set by the packaging converter rather than by raw resin alone. Heat-seal initiation is characterised on a gradient heat-seal tester at 0.5 MPa jaw pressure and 1 s dwell, while package-level hot-tack is measured by ASTM F1921-12(2018). Food-contact status requires lot-specific supplier documentation; the base olefin chemistry is addressed under FDA 21 CFR 177.1520 for US use and under EU 10/2011 for EU single-use packaging, but final overall migration is tested on the finished laminate per EN 1186-1:2002 and EN 1186-14:2002 against the 10 mg/dm² limit.
A low-crystallinity VLDPE modifier is introduced into injection-grade PP homopolymer compounding at 10–25 wt% inside a co-rotating twin-screw extruder with L/D 40:1 and segmented conveying/kneading elements. A representative formulation for soft-touch interior trims contains 72 wt% PP homopolymer, 18 wt% DF710, and 10 wt% talc with median particle diameter near 1.5 µm; the talc is metered through a downstream side feeder at barrel 7 so that the VLDPE phase is not exposed to first-stage melting shear that would over-disperse the low-melting droplets. Barrel settings from feed throat to die are typically 180 °C, 190 °C, 200 °C, 210 °C, 220 °C, with vacuum devolatilisation at -0.08 MPa in barrel 9. A high-mixing screw configuration with two kneading zones—first at 45° stagger for dispersion of DF710 droplets and second at 90° for talc distribution—prevents low-viscosity VLDPE from encapsulating filler particles. Actual melt temperature measured at the die exit is kept below 240 °C; above this threshold, odour and yellowing appear in subsequent injection moulding. Shutdown purging uses PP homopolymer before production stops so that low-melting DF710 does not solidify and seal downstream screen packs or die inserts. Impact testing per ASTM D256-23 shows improvement at 23 °C relative to neat PP, but the rate of improvement flattens beyond 20 wt% because the dispersed phase reduces flexural modulus measured per ISO 178:2019 at an accelerating rate. If DF710 exceeds 25 wt%, injection-moulded plaques on a 1500 kN clamp machine develop surface haze and uneven gloss, especially when the mould surface is below 30 °C; hot runners should be held at 230 °C and mould temperature at 40 °C. Low-temperature ductility at -30 °C is controlled by the α-olefin sequence distribution of the VLDPE, not by compounding temperature alone. Automotive interior release testing is performed by VDA 278 for VOC/FOG, but the finished article must still pass vehicle-level chamber limits. Pre-drying at 60 °C for 2 h is applied only when talc moisture exceeds 0.15 wt%; polyolefin hydrolysis is not a primary degradation pathway, but surface moisture creates splay at the die. Published data for this specific talc/VLDPE/PP configuration remains limited; production trials quantify the exact impact-to-stiffness trade-off.
Halogen-free flame-retardant cable sheathing formulations incorporating DF710 are typically based on EVA with vinyl acetate content of 26–28 wt% and synthetic magnesium dihydroxide or precipitated alumina trihydrate at 150–180 phr. The VLDPE contributes low-temperature flexibility after mineral filler loading, evidenced by elongation at break retention when tested per IEC 60811-501:2012; its lower crystalline melting range reduces stiffening caused by filler network formation. Compounding is performed in an internal mixer with a drop temperature of 165–175 °C because alumina trihydrate releases structured water above 180 °C, and premature dehydration causes vacuoles and surface roughness in the final jacket. After pelletising, the jacket is extruded on a single-screw extruder with L/D 30:1 and a barrier screw at a die-head temperature of 130–150 °C. The melt strength of the filled compound is lower than that of filled EVA, so the water-trough temperature is maintained at 20–25 °C and drawdown ratio is kept below 3:1; exceeding this ratio produces longitudinal surface microcracks that propagate during cable bending tests. Undispersed mineral agglomerates larger than 20 µm are screened by a 100 mesh screen pack at the extruder adapter; pressure drop across the pack is monitored and a filter change is required when differential pressure exceeds 5 MPa. The extruder melt pump operates at 15–25 MPa head pressure. Flame retardancy of the finished single-core cable is assessed through IEC 60332-1-2:2015, smoke density through IEC 61034-2:2019, and acid gas evolution through IEC 60754-2:2011. A process boundary exists in hot-set behaviour: formulations based on uncrosslinked DF710 are not recommended for insulation layers exposed to long-term conductor temperatures above 90 °C; crosslinked or higher-melting matrices are more suitable when the conductor is rated beyond that level.
| Test standard | Parameter examined | Typical pass benchmark |
|---|---|---|
| IEC 60332-1-2:2015 | Vertical flame propagation in single insulated wire/cable | Flaming stops within 60 s and damage zone does not propagate to upper support |
| IEC 61034-2:2019 | Smoke density in specified chamber | Light transmittance ≥ 60% depending cable class |
| IEC 60754-2:2011 | Acid gas evolution from combustion | pH ≥ 4.3 and conductivity ≤ 10 µS/mm |
| IEC 60811-501:2012 | Mechanical properties of sheathing compounds | Elongation retention after ageing per product specification |
Hot-melt adhesive formulations built around a low-crystallinity olefin backbone with a melting peak near 55 °C extend open time and improve low-energy polyolefin adhesion in lamination and carton sealing. TAFMER DF710 is loaded at 20–35 wt% together with a hydrocarbon or rosin-ester tackifier, a synthetic wax, and a hindered phenolic antioxidant at 0.5–1.0 wt%. Mixing is performed in a jacketed vertical mixer at 150–170 °C under a nitrogen blanket maintained at positive pressure of 0.05–0.10 bar; the melt is then slot-die coated at 160–175 °C onto release paper at coating weights of 10–30 g/m². The upper temperature constraint is severe: residence time above 190 °C must not exceed 30 min, because viscosity drift and gel-particle formation are accelerated by oxygen ingress at the mixer shaft seals. Viscosity stability is checked with a Brookfield thermosel system at 180 °C; a viscosity drift above 20% after 1 h indicates antioxidant depletion. Final adhesion is measured by loop tack per ASTM D6195-22 and shear adhesion failure temperature per ASTM D4498-07(2021); cohesive strength determines failure mode more than interfacial wetting on untreated polyolefin surfaces. For food packaging lamination adhesives, the final formulation must satisfy FDA 21 CFR 175.105 or regional equivalents, but neat resin compliance alone does not guarantee formulated adhesive compliance due to tackifier migration. Finished goods include olefin label pressure-sensitive adhesives and closure adhesives for coated board. Published formulation data for DF710 in hot-melt systems is limited; tackifier compatibility and cloud point must be confirmed by pilot melt-blending before production scale-up.
When a soft-touch overmoulded layer is required without secondary coating, DF710 is introduced into the soft layer at 40–60 wt% with a PP random copolymer and an olefinic compatibiliser to reduce the layer modulus. The rigid PP substrate is moulded first on a rotary platen machine with clamp force in the 1200–1800 kN range, then the soft layer is shot at 180–200 °C into a core-back or slide-mould cavity held at 30–40 °C. Melt fusion between the two layers is mechanical and requires no primer, but the surface temperature of the rigid PP insert must remain above 100 °C at the interface for reliable interlock. Injection speed of 100–200 mm/s at the soft layer prevents premature freeze-off; thick sections above 2.0 mm require pack pressure profile of 40–60 MPa followed by 3–5 s hold. A production failure mode in high-DF710 formulations is gate blush and gas entrapment; sequential valve gating with a holding pressure of 40–60 MPa and a decompression stroke before gate opening reduces the defect. Hardness of the soft layer is measured with a Shore A durometer per ISO 868:2003 and adjusted by the PP/VLDPE ratio; components should not be exposed to continuous service temperatures above 80 °C because low crystalline melting reduces dimensional stability. Textured mould surfaces are preferred to glossy finishes to mask gate blush. Finished articles include power-tool overmoulds, appliance feet, and medical device handgrips. For automotive interior components, fogging and odour are assessed per DIN 75201:2011 or VDA 270. Chemical exposure to hydrocarbons or strong oxygenated solvents causes swelling of the DF710-modified layer; compatibility testing is required before use in fuel-contact environments.
Medical flexible films and tubing demand low bending stiffness and acceptable clarity without phthalate plasticisers. DF710 is extruded as a soft polyolefin layer inside a multilayer construction with PP or polyethylene contact layers; the low density of 0.870 g/cm³ reduces bending stiffness and improves drape in pouches. Cast-film processing uses a 0.5–0.8 mm die gap and melt temperature of 200–220 °C to produce film in the 80–150 µm thickness range. Tubing extrusion runs on a single-screw extruder with L/D 25:1 and an annular die gap of 0.8–1.2 mm, with durometer tested per ISO 868:2003. Surface activation by corona discharge at 38–42 mN/m surface energy is required for lamination to PET or nylon layers; surface energy is tested per ISO 8296:2003. Cleanroom extrusion under ISO 14644-1:2015 Class 8 reduces particulate contamination risk, but no uniform cleanroom class is mandated for all medical devices. Sterilisation compatibility is not automatic: ethylene oxide processing per ISO 11135:2014 can alter residual stress distribution, and repeated saturated steam exposure above 121 °C is outside the practical use range for unmodified VLDPE because of dimensional distortion risk. Residual ethylene oxide is evaluated per ISO 10993-7:2008 with extended aeration at 45 °C for 72 h where required. Final device biocompatibility is evaluated under ISO 10993-1:2018, with cytotoxicity per ISO 10993-5:2009, sensitisation per ISO 10993-10:2010, and material-mediated pyrogenicity where fluid contact duration warrants. Extractables and leachables are assessed on the finished medical article, not on the raw resin, under ISO 10993-18:2020. Published data for DF710 in medical device construction is limited; each manufacturing site must qualify lot-to-lot consistency of volatile content and catalyst residues before validation batches.
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