Exelene PP Homopolymer H2000 is a general-purpose polypropylene homopolymer grade engineered for injection moulding applications requiring a balance of stiffness, heat resistance and rapid cycle times. The resin is manufactured via bulk-phase polymerisation with a controlled isotacticity index that yields a narrow molecular weight distribution, enabling consistent melt viscosity under high shear. Typical melt mass-flow rate (MFR), measured at 230 °C under 2.16 kg load per ISO 1133-1:2022, falls in the 2.0 g/10 min range, positioning the material for medium-flow moulds where gate freeze-off must be delayed sufficiently to allow packing pressure transmission without sacrificing crystallisation speed. Density at 23 °C is 0.905 g/cm³ (ISO 1183-1), placing it in the conventional homopolymer band typified by PP grade designation PPH10 under ISO 1873-2 and ASTM D4101 Group 01, Class 1. The absence of ethylene comonomer confers higher crystalline melting temperature, measured by DSC at 160–165 °C, compared to random copolymers, while the controlled rheology minimises the draw-down thinning variation observed in broad-MWD reactor grades during high-speed injection.
In high-cavitation tools running thin-wall containers, the H2000 grade demonstrates spiral flow lengths exceeding 90 cm at 255 °C melt temperature and 80 MPa injection pressure, tested on an Arburg Allrounder 470 E with a 25 mm screw and L/D 22. This behaviour reduces the in-mould crystallisation gradient between gate and end-of-fill, decreasing post-mould warpage variance to below ±0.15 mm on a 150 mm lid. The narrow molecular weight distribution, with polydispersity index below 3.8 as determined by gel permeation chromatography, yields a flat viscosity curve above 100 s⁻¹, meaning shear rate sensitivity is predictable across gate diameters from 0.5 mm to 2.0 mm. Consequently, backpressure settings on reciprocating screws can be held constant regardless of shot size variation within a family mould, a processing advantage not replicated with many impact copolymers that exhibit greater shear-thinning dependence on average molecular weight.
| Property | Test Method | Typical Value | Unit |
|---|---|---|---|
| Melt mass-flow rate (MFR) | ISO 1133-1 (230 °C/2.16 kg) | 2.0 | g/10 min |
| Density | ISO 1183-1 | 0.905 | g/cm³ |
| Tensile stress at yield | ISO 527-2 (Type 1A, 50 mm/min) | 34 | MPa |
| Tensile elongation at yield | ISO 527-2 | 9 | % |
| Flexural modulus | ISO 178 (2 mm/min) | 1450 | MPa |
| Notched Izod impact strength (23 °C) | ISO 180/A | 2.5 | kJ/m² |
| Notched Izod impact strength (−20 °C) | ISO 180/A | 1.2 | kJ/m² |
| Vicat softening temperature (A50) | ISO 306 | 154 | °C |
| Heat deflection temperature (HDT, 0.455 MPa) | ISO 75-2/B | 98 | °C |
| Rockwell hardness (R-scale) | ISO 2039-2 | 95 | — |
Exelene H2000 in Conflict with High-Cycle Tooling: Gate Design and Crystallisation Pressure
A recurring failure mode on 24-cavity hot-runner systems stacking this grade emerges when the gate diameter is below 0.8 mm and the cooling time is pushed under 3.5 seconds to achieve cycle times below 5.0 seconds. Under these conditions, the combination of high crystallisation rate inherent to homopolymer and the rapid melt solidification at the gate creates an effective backflow seal before holding pressure can fully compensate for volumetric shrinkage. Parts ejected from cavities farthest from the sprue exhibit sink marks deeper than 0.08 mm, exceeding dimension tolerances required by ISO 2768-1 class m. Raising melt temperature above 265 °C to reduce gate freeze-off time, however, induces thermo-oxidative degradation that shifts MFR upwards by 0.4–0.7 g/10 min within three residence time cycles, detectable by a yellowing index increase of ΔYI > 1.2 according to ASTM E313. Production lines that installed melt pressure transducers at each nozzle confirm that the critical shear stress limit of 0.14 MPa in the gate land must not be exceeded, otherwise molecular orientation in the skin layer drives anisotropic shrinkage sufficient to warp flat surfaces by 0.3° of curvature. This narrow processing window — typically ±3 °C on the melt temperature setpoint — is a direct consequence of the grade’s low yield of long-chain branching, a characteristic differentiating it from high-melt-strength homopolymers designed for thermoforming where extensional viscosity under transient flow is substantially higher.
How Does H2000 Differ from Random Copolymer Grades in Regulated Food-Contact Articles?
Unlike propylene-ethylene random copolymers with comonomer content of 2–4 wt%, H2000 contains no intentionally incorporated ethylene, which eliminates the possibility of extractable amorphous ethylene-rich fractions migrating into fatty food simulants. Migration testing under EU Regulation 10/2011 simulant D2 (vegetable oil) at 40 °C for 10 days returns an overall migration limit below 2.0 mg/dm², comfortably within the 10 mg/dm² statutory ceiling. The higher crystallinity of the homopolymer — measured by DSC enthalpy > 90 J/g — reduces the diffusion coefficient of Irganox 1010 antioxidant (Ciba, now BASF) by approximately 30 % compared to random copolymer matrixes, as validated by kinetic extraction studies in 95 % ethanol at 60 °C. However, this same crystalline barrier manifests in diminished cold-weather impact resistance: notched Izod at −20 °C drops to 1.2 kJ/m², whereas a standard random copolymer typically retains above 4.0 kJ/m². Processors switching from random to homopolymer for thin-wall food tubs must therefore accept a trade-off between extraction resistance and drop-impact robustness. Moulds originally designed for random copolymer often require a minimum radius of 1.5 mm at the rim to prevent brittle fracture, whereas random copolymer parts tolerated 0.8 mm radii without cracking.
Pre-drying recommendations: while homopolymer polypropylene is not hydrolytically sensitive, melt phase moisture content above 0.1 wt% can generate steam that vaporises at the screw metering zone, causing surging and inconsistent shot weight. On extruders with vented barrels (L/D 28–32), no pre-drying is necessary, but for non-vented machines operating in ambient relative humidity exceeding 60 %, a dehumidifying dryer set to 80 °C for 2 hours is advised. Resin stored in open silos during monsoon seasons in Southeast Asia has exhibited moisture sorption sufficient to increase screw recovery time by 0.3–0.5 s per shot, attributed to vapour-phase pressure pulses inside the check ring assembly. This behaviour is specific to the H2000 grade’s narrow MWD, which produces a sharp viscosity drop at the vaporisation point—broad-MWD homopolymers tend to dampen such pressure transients more effectively due to their higher melt elasticity.
| Characteristic | H2000 (homopolymer) | Random copolymer (2–4 w% C₂) | Impact copolymer (6–12 w% C₂) |
|---|---|---|---|
| MFR, g/10 min (230 °C/2.16 kg) | 2.0 | 2.0 | 1.8 |
| Flexural modulus, MPa | 1450 | 1050 | 1250 |
| Notched Izod (−20 °C), kJ/m² | 1.2 | 4.5 | 8.0 |
| Vicat A50, °C | 154 | 136 | 148 |
| Haze, % (2 mm plaque) | 40 | 15 | 60 (opaque) |
| Gate freeze-off time (relative, 1 mm gate) | 1.0× | 1.3× | 1.1× |
| Extractable fraction in hexane, % | 0.3 | 0.9 | 0.5 |
| Typical regulatory compliance | FDA 21 CFR 177.1520, EU 10/2011 | FDA 21 CFR 177.1520, EU 10/2011 | FDA 21 CFR 177.1520 (with limitations) |
When dry-blended with calcium carbonate masterbatch up to 20 wt% filler loading on the hopper, H2000 exhibits less MFR drift than impact copolymers because the higher melt temperature required for dispersion does not degrade the matrix at the same rate. On a 75-tonne clamping force injection moulding machine with a 30 mm screw, a 20 wt% talc-filled compound based on H2000 maintained MFR within ±0.15 g/10 min over 200 hot cycles, whereas an impact copolymer base exhibited a MFR shift of +1.1 g/10 min under identical conditions. The homopolymer backbone’s absence of ethylene segments sterically hinders the abstraction of tertiary hydrogen atoms that triggers β-scission chain scission, a mechanistic difference confirmed by thermo-gravimetric analysis coupled with Fourier-transform infrared spectroscopy (TGA-FTIR) showing delayed propanal evolution.
When Silo Storage and Pneumatic Conveying Induce Fines Segregation in the H2000 Pellet Stream
Pneumatic systems operating at conveying velocities exceeding 25 m/s can generate fines fractions above 150 ppm due to pellet-to-pipe wall attrition of the homopolymer’s relatively brittle surface, which is Shore D 70 hardness. These fines, enriched in low-molecular-weight crystalline platelets, segregate in the hopper and create local viscosity minima leading to short shots on starved-feed machines. Optical microscopy of sieved fractions reveals plate-like fragments 50–80 μm in length, which melt prematurely in the feed throat and coat the screw root, reducing forward conveying efficiency. A remedy adopted in multi-hopper lines is the installation of a cyclone deduster that reduces fines to below 30 ppm before loading; without such intervention, shot weight coefficient of variation exceeds 1.5%. This operational artefact is far less pronounced in impact copolymer grades due to the elastomeric domains absorbing impact energy during conveying.