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Exelene C2004 PP Copolymer

    • Product Name: Exelene C2004 PP Copolymer
    • Factroy Site: Yudu County, Ganzhou, Jiangxi, China
    • Price Inquiry: admin@ascent-chem.com
    • Manufacturer: Ascent Petrochem Holdings Co., Limited
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    Specifications
    HS Code 416537
    Mfr 230c 2 16kg 4.0 g/10min
    Density 0.90 g/cm³
    Tensile Strength At Yield 26 MPa
    Elongation At Break 50%
    Flexural Modulus 900 MPa
    Izod Impact Notched 23c 10 kJ/m²
    Heat Deflection Temperature 0 45mpa 85 °C
    Vicat Softening Temperature 145 °C
    Melting Point 160 °C
    Rockwell Hardness R90

    As an accredited Exelene C2004 PP Copolymer factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Exelene C2004 PP Copolymer is supplied in 25 kg woven polypropylene bags with an inner liner, ensuring safe handling and storage.
    Container Loading (20′ FCL) 20′ FCL of Exelene C2004 PP copolymer, packed in palletized woven bags, secure, dry, and contamination-free for safe transport.
    Shipping Exelene C2004 PP Copolymer ships as non-hazardous polymer pellets in sealed multi-layer bags or FIBCs. Store away from heat, ignition sources, and direct sunlight. Keep dry during transport to prevent moisture absorption. Ensure proper labeling, secure loading, and ventilation in shipping containers.
    Storage Store Exelene C2004 PP Copolymer in a cool, dry, well-ventilated area, away from direct sunlight, heat, and ignition sources. Keep containers tightly sealed to prevent moisture contamination and maintain product integrity. Avoid contact with strong oxidizing agents. Store on suitable shelving, protected from physical damage and incompatible materials.
    Shelf Life Shelf life is typically 12 months from date of manufacture when stored in original, unopened packaging in dry, cool conditions.
    Application of Exelene C2004 PP Copolymer

    Processing Exelene C2004 PP copolymer into injection-moulded automotive interior trim components—instrument panel lower sections, glove box assemblies, door panel inserts, and B-pillar covers—requires simultaneous control of low-temperature impact resistance and cabin atmosphere emissions. The material is compounded with 20–25 wt% fine talc masterbatch (d₅₀ ≤ 5 µm) to elevate flexural modulus towards 2,800 MPa (ISO 178:2019) while retaining a notched Charpy impact exceeding 8 kJ/m² at −30 °C (ISO 179-1/1eA). A phenolic/phosphite antioxidant package (Irganox B 225 at 0.2 wt%) and a zeolite-based odour scavenger (1.5 wt%) are dry-blended before feeding to a vented single-screw extruder for pre-compounding or directly metered at the injection unit. Processors running 1,500–2,800 t clamp force machines with accumulator-assisted injection units set melt temperature at 230–245 °C measured at the nozzle, mould wall temperature at 30–50 °C, hydraulic back pressure at 8–12 bar, and hold pressure decay over 4–8 s. Sequential valve-gate control prevents visible knit lines across the Class A surface. Residence time must not exceed 5 min at 245 °C; beyond this threshold random chain scission generates aldehydes and ketones that push total volatile organic compound (TVOC) emissions above the 100 µg/g limit per VDA 278 (2011). Fogging condensate mass per DIN 75201-B is routinely held below 2 mg, and VDA 270 odour rating stays at grade 2.0–2.5 after 24 h conditioning at 80 °C. A critical bottleneck observed on multi-cavity door trim tools is post-demould distortion when the de-mould temperature exceeds 85 °C; hence core cooling circuits are fed with chilled water at 12–15 °C and mould-open time is kept below 2.5 s. Field audits from tier-1 suppliers confirm that batch-to-batch variability in the talc aspect ratio shifts the coefficient of linear thermal expansion (CLTE) by ±8%, causing mismatch with adjacent polyolefin elastomer skins during thermal cycling tests (−40 °C to +90 °C per OEM specification). Therefore inline CLTE measurement on moulded plaques using a thermomechanical analyser (TMA) is integrated into production-part approval process (PPAP) submissions.

    What Happens When Melt Flow Exceeds 20 g/10 min in High-Speed Injection Moulding?

    When the melt flow rate (MFR) of Exelene C2004—measured at 230 °C/2.16 kg per ISO 1133-1:2022—crosses 20 g/10 min, the low-molecular-weight fraction enables filling of thin-walled dairy containers with flow length-to-wall thickness (L/t) ratios exceeding 350. Yoghurt cups, creamer tubs, and ice cream boxes with nominal wall thicknesses between 0.40 mm and 0.80 mm are moulded on high-speed toggle presses with injection pressures peaking at 1,800–2,200 bar and screw-forward speeds of 300–500 mm/s. A hot-runner manifold maintained at 235 °C directs the stream into 48- or 64-cavity stack moulds fitted with conformally cooled cores. Cycle times as low as 2.8–3.5 s demand extremely rapid crystallisation; hence 0.08–0.12 wt% of a sorbitol-based or phosphate ester nucleating agent (e.g. HPN-20E) is incorporated to raise the crystallization onset temperature to approximately 128 °C and narrow the DSC peak width to 4–6 °C. A calcium stearate acid scavenger at 0.05 wt% and a low-fogging antistat at 0.15 wt% complete the dry-blend formulation. The high shear rates generated—calculated as 10⁵ s⁻¹ at the gate—induce adiabatic heating of 15–25 °C above the set melt temperature. Operators compensate by lowering the barrel mid-zone settings to 210–225 °C to maintain a true melt stream near 242 °C and avoid thermal flash near the sprue. Silver streaks emerge when the equilibrium moisture content in the copolymer exceeds 0.03%; closed-loop desiccant drying at 80 °C for 3–4 h to a dew point of −35 °C is mandatory at ambient relative humidity > 60%. Food-contact compliance is demonstrated through overall migration testing per EN 1186-1:2002, yielding extracts below 10 mg/dm² in simulant B (3% acetic acid) for 10 d at 40 °C, and specific migration of antimony from catalyst residues remains below 0.04 mg/kg per EU Regulation No 10/2011 Annex II. The US FDA 21 CFR 177.1520(c) table 3.2a classification covers polymer repeating units; successful condition-of-use mapping restricts these containers to refrigerated or ambient filling—hot-fill above 85 °C collapses sidewalls due to a heat deflection temperature (HDT B, 0.45 MPa) of only 98 °C for the talc-free neat copolymer. Moulders report that gate blush can be eliminated by reducing the first-stage injection velocity to 80% of the peak and switching to pressure control via cavity-pressure transducers at 400 bar.

    White goods structural housings produced from Exelene C2004—washing machine outer tub rings, dishwasher base frames, and tumble dryer front panels—utilise a pre-compounded 30 wt% talc-filled formulation dry-blended with 5 wt% of an ethylene-propylene elastomer impact modifier to achieve a room-temperature notched Izod impact of 12–15 kJ/m² (ASTM D256, Method A) without sacrificing the 2,600 MPa flexural modulus target under ISO 178. The compound is injection moulded on 2,500 t two-platen machines with gas-assisted injection for hollow stiffening ribs that reduce warpage along the 800 mm span of a washer ring. Melt temperatures span 225–240 °C, mould temperature 35–45 °C, and gas injection delay is set at 2.0 s after the melt front reaches the rib gate. Glow wire testing per IEC 60335-1:2020 clause 30.2.3 requires ignition temperature (GWIT) exceeding 775 °C on finished parts of 3.0 mm thickness; the talc loading and bromine-free stabilisation package routinely pass 750 °C glow wire without flame for 30 s. A production-scale bottleneck arises from the abrasive nature of slow-cooling talc-filled melts near sprues: nitrided screws with L/D 24:1 and bimetallic barrels are specified to survive 8,000 h campaigns before screw diameter loss exceeds 0.3 mm. During EU Ecodesign implementation, some converters attempted lightweighting to 2.2 mm wall stock; microphone-recorded noise radiation increased by 4 dB(A) in the 200–400 Hz band under out-of-balance loads, forcing a return to 2.8 mm critical rib thickness with FEM-assisted acoustic simulations.

    Exelene C2004 PP copolymer is injection moulded into open-head industrial pails and tight-head transport drums of 5–25 L nominal capacity, carrying UN dangerous goods packaging certification under UN 1H2 (plastics drums, non-removable head) test series. The pail body, gasket seat, and lid are produced in a 2+2 stack mould with sequentially collapsing core rings. The base copolymer is tinted with 2.0 wt% carbon-black masterbatch for UV stabilisation; no mineral filler is added, preserving the copolymer’s intrinsic low-temperature ductility. A 3–5 wt% metallocene plastomer grafted with maleic anhydride is let down to raise the multi-axial impact energy at −18 °C beyond 40 J (ISO 6603-2, puncture at 4.4 m/s), the critical threshold for the 1.8 m drop test onto a rigid target. Stacked-load compression at 40 °C for 28 d (UN test method) demands a creep modulus > 1,200 MPa; the part design incorporates a tapered wall increasing from 2.0 mm at the rim to 3.5 mm at the bottom chime. Cycle time on a 1,000 t injection machine runs at 11–13 s, limited by gate freeze at 3.5 s and the cooling-time constant for the bottom thickening. Shrinkage across the diameter is 1.4–1.6%; the ovality of stacked empty pails must stay within 2.0 mm to pass automated palletising, requiring a ring gauge check and conditioning at 50 °C/48 h for post-moulding crystallisation completion. A recurrent field failure in tropical climates is stress-cracking at the handle attachment boss when detergent-filled pails are subjected to cyclic lifting at 38 °C, 85% RH—eliminated by hot-stamping a polyolefin-foam gasket that displaces tensile stress from the knit line.

    When Post-Consumer Recyclate Enters the Matrix

    When converters blend post-consumer recyclate (PCR) derived from mixed-colour PP copolymer crates with virgin Exelene C2004 for injection-moulded storage boxes, toy blocks, and flower pots, the processing envelope contracts sharply. A 30 wt% PCR incoming fraction typically lowers the MFR of the blend by 3–5 g/10 min due to crosslinking induced by prior thermal-oxidative history, and increases the incipient melt viscosity at 1 s⁻¹ by 15–22%. A twin-screw compounding step (co-rotating, 40:1 L/D) with 0.15 wt% peroxide-free restabiliser masterbatch and 2.0 wt% polypropylene-graft-maleic anhydride (PP-g-MA, MA content 1.0%) re-equalises the MFR to within ±1.5 g/10 min of the virgin material. During injection moulding of the compound, screen packs of 200–400 µm mesh size are inserted in the nozzle adapter to trap non-meltable contaminants; nozzle pressure drop increases by 40–80 bar and mandates cleaning every 8 h on 500 t presses. The finished article must comply with REACH Annex XVII entry 50, restricting the sum of eight carcinogenic polycyclic aromatic hydrocarbons (PAHs) to < 1 mg/kg in consumer articles, as verified by GC-MS after toluene extraction per AfPS GS 2019:01 PAK. Because odour originating from degraded PCR limits use in indoor consumer goods, processors deploy a vacuum degassing unit on the extruder barrel with zone pressure −0.8 bar and add 0.4 wt% activated carbon-loaded polyolefin carrier to reduce sensory defects to VDA 270 grade 3.0. Published data for this specific Exelene C2004/PCR configuration indicates a Gardner impact drop of 20–30% relative to fully virgin mouldings at 25% PCR loading when tested per ASTM D5420; the failure mode transitions from ductile puncture to brittle cracking at −5 °C.

    Application SectorTypical Formulation Additives (wt% on copolymer)Key Quantitative Property (TestMethod)Target Range
    Automotive interior trim20–25% talc, 1.5% zeolite scavenger, 0.2% AO B225Charpy notched impact, −30 °C (ISO 179-1/1eA)>8 kJ/m²
    Thin-wall dairy cups0.08% nucleant, 0.05% CaSt, 0.15% antistatSpiral flow length, 2 mm × 10 mm channel at 1,000 bar>65 cm
    White goods structural frame30% talc, 5% elastomer modifierFlexural modulus (ISO 178)2,600–3,000 MPa
    UN-certified industrial pail2% carbon black MB, 3–5% plastomer-g-MAHPuncture energy at −18 °C, 4.4 m/s (ISO 6603-2)>40 J
    Post-consumer recycled box30% PCR, 2% PP-g-MA, 0.15% restabiliserMFR (ISO 1133-1, 230 °C, 2.16 kg)16–22 g/10 min
    Medical device housing0.3% permanent antistat, 2% TiO₂ MB, rad stabiliser packageNotched Izod impact (ASTM D256, Method A)>10 kJ/m²
    Beverage closure0.1% erucamide, 0.08% nucleant, 0.02% antioxidantRemoval torque after 48 h at 23 °C1.0–2.5 Nm

    Medical equipment housings—handheld diagnostic meter shells, nebuliser compressor covers, and bench-top analyser bezels—are injection moulded from Exelene C2004 in ISO 14644-1 class 8 cleanrooms after exhaustive material qualification under ISO 10993-5:2009 (cytotoxicity, MEM elution) and ISO 10993-10:2010 (skin irritation and delayed-type hypersensitivity). The polymer resin is supplied with a drug master file-type regulatory support package; converters pre-dry at 90 °C for 4 h in dedicated stainless-steel hoppers to reduce volatile condensable substances below 0.05%. A permanent non-amine-based antistatic additive at 0.3 wt% and a gamma-stable TiO₂ colour masterbatch at 2.0 wt% constitute the only allowable modification. Mould temperature is limited to 25 °C to avoid blooming of lipid-soluble oligomers, and barrel residence time is capped at 3 min. Sterilisation by ethylene oxide (EO) is performed at 55 °C followed by forced aeration for 72 h to reduce residual EO below 1 µg/g; when gamma irradiation at 25 kGy is specified, a rad-stabiliser package based on hindered amine light stabiliser (HALS) plus a secondary aryl phosphate prevents post-irradiation yellowing to a ΔYI < 5 after accelerated aging at 60 °C for 7 d (ASTM D6290). No formulation containing intentional di(2-ethylhexyl) phthalate (DEHP) or other low-molecular-weight ortho-phthalate plasticisers is permitted—this aligns the part with the Medical Devices Regulation (EU) 2017/745 Annex I essential safety requirement 10.4 on endocrine-disrupting substances. A failure mode recorded on a diagnostic reader chassis involved brittle fracture at the snap-fit after two EtO cycles due to physical aging-driven free volume collapse; the issue was mitigated by changing the gate location to induce a transverse rather than flow-directional orientation at the snap arm and adopting a stress-relief annealing step of 100 °C/2 h post-moulding.

    Caps and Closures: A Different Rheological Profile

    Two-piece beverage closures injection moulded from Exelene C2004 deviate from the high-speed thin-wall rulebook because tamper-evident band bridging and linerless seal integrity depend on controlled neck finish replication rather than extreme L/t capability. The copolymer is formulated with 0.08–0.12 wt% of a sorbitol-based clarifying/nucleating agent to produce a haze value below 35% at 1.2 mm thickness (ASTM D1003) and 0.1 wt% of an unsaturated fatty amide slip additive (erucamide) that undergoes field migration to the moulding surface over 24–72 h, reducing the coefficient of friction to 0.20–0.30. Melt temperature is kept within a narrow band of 215–230 °C; above 230 °C the erucamide begins volatilising at the hot-runner gate, forming plate-out on the cavity surface within 4 h of continuous operation. Mould cooling water at 8–12 °C chills the neck ring and core to achieve a 3.5 s cycle and freeze the undercuts; dimensional tolerance on the inner diameter is held to ±0.05 mm to match the blow-moulded PET or HDPE bottle finish. Offline application torque and removal torque are measured per ASTM D3469; removal torque must fall between 1.0 Nm and 2.2 Nm after 48 h conditioning at 23 °C. EU No 10/2011 Amendment 2020/1245 sets a specific migration limit for erucamide at 5 mg/kg food simulant; the low loading and subsequent surface bloom ensure compliance via simulation demonstrating that the surface-contact layer exhausts extractable amide below the regulatory threshold. Environmental stress crack resistance (ESCR) under cap-thread pressure is validated by capping carbonated soft drink bottles at 4.0 volumes CO₂ and performing a 24 h, 40 °C tilt test (modified ASTM D2561); slit propagation exceeding 15% of thread height constitutes a fail. Moulders running 96-cavity systems report that uneven core cooling induces a 0.03–0.06 mm ovality drift correlated with cycle-time scatter of only 0.3 s, necessitating independent core temperature control loops per each stack level.

    Thin-wall in-mould labelling (IML) transforms Exelene C2004 into decorated ice cream containers, margarine tubs, and chilled-food pails with a wall stock of 0.45–0.65 mm through a fully automated process that fuses the label—either a cast PP film or a multi-layer barrier lamination—directly into the cavity. A robot places the die-cut label held by electrostatic pins; within 0.2 s the mould closes and the copolymer melt at 230–245 °C is injected behind the label at 350–450 mm/s. To prevent label wash-out at the gate and distortion along the rim, the material carries a tailored rheology package comprising 0.05 wt% of a fluoropolymer-based processing aid that suppresses melt fracture and 0.08 wt% of a high-crystallinity nucleator that sets a fast free-off time. No external mould release is permitted; therefore the compound includes 0.06 wt% of a glycerol monostearate antistatic agent to facilitate label demoulding and static dissipation for downstream conveying. Cycle time on a 4-cavity IML system is trimmed to 2.9–3.8 s; cooling time is the rate-limiting step, shortened by bubble-free conformal cooling channels machined within 0.5 mm of the cavity surface. Food-contact conformance relies on the same EU No 10/2011 overall migration < 10 mg/dm² and the US FDA 21 CFR 177.1520 classification; the label adhesive tie-layer must not contain primary aromatic amines detectable above 0.01 mg/kg in the finished article, tested per EN 13130-1:2004. When a multi-layer barrier label is employed, the differential shrinkage between label (0.8–1.2%) and copolymer substrate (1.5–1.8%) causes curl after storage at −25 °C; this is counteracted by co-crystallising the label with 15% of a low-isotacticity PP that matches the post-moulding contraction profile. Production-scale observations document that static charge on the label surface above 5 kV leads to mis-placement and double-sheet feeding; conditioning the IML magazine room to 55 ± 5% RH and 22 ± 2 °C suppresses triboelectric charging to an acceptable 1–2 kV.

    Regulatory DomainStandard / MethodTest ParameterAcceptance Criterion for Copolymer Part
    EU Food Contact—PlasticsEU 10/2011 Annex VOverall migration, simulant B, 10 d/40 °C< 10 mg/dm²
    FDA Food Contact21 CFR 177.1520(c) table 3Polymer composition and extractivesNo chloroform-soluble fraction > 6.4% for fully formulated compound
    Automotive EmissionsVDA 278:2011TVOC 90 °C/30 min headspace< 100 µg/g
    Automotive FoggingDIN 75201-B:1992Fogging condensate mass, 100 °C/16 h< 2 mg
    Household Appliances SafetyIEC 60335-1:2020 clause 30.2Glow wire flammability at 750 °CNo ignition, or flame extinguishes within 30 s; tissue paper not ignited
    UN Transport PackagingUN Model Regulations 23rd rev (test 6.1.5.2)Stack load at 40 °C, 28 d, drop at −18 °CNo rupture or leakage; no permanent deformation causing loss of closure integrity
    Medical BiocompatibilityISO 10993-5:2009 & 10993-10:2010Cytotoxicity (MEM), skin irritation, delayed hypersensitivityGrade 0–1 (non-cytotoxic); no erythema/oedema score > 1
    EU REACH – Consumer ArticlesREACH XVII entry 50 (PAH) via AfPS GS 2019:01BaP and sum of 8 PAH, toluene extraction GC-MSBaP < 0.5 mg/kg; sum < 1 mg/kg in rubber/plastic contact parts
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    Certification & Compliance
    More Introduction
    Exelene C2004 is a polypropylene random copolymer engineered for injection-moulded articles requiring a controlled balance between optical transparency and room-temperature impact resistance. The grade carries a nominal melt mass-flow rate of 4 g/10 min when characterised according to ISO 1133-1 (230 °C, 2.16 kg). Ethylene co-monomer content is held within a narrow window—typically 2.8–3.5 wt%—to suppress crystallinity without inducing the phase-separated morphology that characterises heterophasic block copolymers. This compositional restraint yields a flexural modulus near 900 MPa (ISO 178) and a notched Charpy impact strength at 23 °C exceeding 8 kJ/m² (ISO 179-1/1eA), placing the material in a performance corridor where stiffness is sacrificed only marginally relative to a homopolymer while low-temperature ductility remains usable down to approximately 0 °C. Industrial application targets include thin-walled food containers, media packaging, laboratory consumables, and transparent appliance components.

    Melt Processing Window and Rheological Constraints

    Production-scale extrusion and injection moulding of Exelene C2004 proceed on standard single-screw reciprocating equipment with a general-purpose polyolefin screw design, typically a 20–24:1 L/D ratio and a compression ratio between 2.5:1 and 3.0:1. The recommended barrel temperature profile rises from 180 °C in the feed zone to 210–230 °C at the nozzle. Melt temperature as measured by a hand-held pyrometer at the purge should not drift above 245 °C; sustained residence time beyond 5 min at that boundary initiates chain scission detectable as a downward MFR shift greater than 0.8 g/10 min and a measurable yellowing index (YI) increase of +2.5 units according to ASTM D1925. When processing on hot-runner systems with manifold temperatures set above 250 °C, operators report a progressive loss of dart impact strength—often 15–20 % after 8 hours of continuous cycling—attributed to thermo-oxidative degradation of the ethylene-rich sequences. Mould fill analysis indicates that Exelene C2004 behaves as a moderately shear-thinning fluid with a power-law index of approximately 0.32 within the shear-rate window of 10²–10⁴ s⁻¹ at 230 °C. The viscosity-shear profile demands that gate land lengths be kept below 1.0 mm for direct-edge gates; otherwise, melt fracture emerges at injection velocities exceeding 80 mm/s. Pre-drying is not mandatory when packaging remains intact, but exposure to ambient conditions at relative humidity above 60 % for more than 4 hours introduces surface moisture sufficient to cause silver streaking and a 12–18 % reduction in weld-line tensile strength under ISO 527-2/1A conditions. Therefore, a desiccant dryer set to 80 °C with a dew point of -30 °C for 2 hours is specified whenever logistical moisture pick-up is suspected. Clamp force requirements are modest; for a cold-runner, 8-cavity mould producing a 0.8 mm wall-thickness tub, a 120-tonne machine is adequate at a specific injection pressure of 700–900 bar hydraulic. However, the low melt rigidity—quantified by a heat deflection temperature of 72 °C under 0.45 MPa (ISO 75-2B)—extends the required cooling time by 10–15 % compared to a homopolymer of equivalent MFR, a point frequently underestimated in cycle-time costing.

    Why Does Exelene C2004 Outperform Homopolymer PP in Contact Clarity Applications?

    The optical signature of a random copolymer is rooted in its crystallite architecture. In Exelene C2004, the statistically distributed ethylene defects reduce the average spherulite diameter to below the wavelength of visible light. A 2 mm injection-moulded plaque recorded a haze value of 12 % and a light transmittance of 88 % per ASTM D1003, whereas a homopolymer with an identical 4 g/10 min MFR yielded haze near 55 % and transmittance around 75 % under the same moulding conditions. The difference becomes commercially decisive in snap-fit closures for cosmetics or in over-caps for personal care products, where brand owners reject visible crystalline clouding. Furthermore, the narrower melting range of C2004 (135–148 °C peak endotherm by DSC at 10 K/min) minimises differential refraction during rapid quench, producing more uniform through-thickness clarity than can be achieved with nucleated homopolymers, even those co-additivated with 0.15 % sorbitol-based clarifier. A secondary benefit emerges during hot-fill testing. Containers moulded from Exelene C2004 withstood 85 °C water-bath immersion for 30 seconds without visible blushing or panel deformation, a threshold sufficient for pasteurised dairy and juice packaging. Although this performance is inferior to that of clarified homopolymer with HDT/B values above 105 °C, it obviates the need for a post-mould annealing step that adds equipment capital and energy cost. Transparent polypropylene containers in refrigerated distribution often collide with ethylene-vinyl alcohol barrier laminates; here, the random copolymer’s seal initiation temperature of 115 °C (ASTM F2029) allows heat-seal compatibility with PE-based sealant webs without warping the PP substrate. These multi-material structures are outside the scope of monolayer homopolymer processing entirely.
    Comparative physical properties across polypropylene grades (injection-moulded, conditioned 40 h at 23 °C/50 % RH)
    PropertyTest MethodExelene C2004 (Random Copolymer)PP Homopolymer (MFR 4)PP Heterophasic Copolymer (MFR 4)
    Melt mass-flow rate (230 °C/2.16 kg)ISO 1133-14.0 g/10 min4.0 g/10 min4.0 g/10 min
    Tensile modulusISO 527-2/1A950 MPa1550 MPa1100 MPa
    Tensile yield stressISO 527-2/1A24 MPa35 MPa22 MPa
    Notched Charpy impact (23 °C)ISO 179-1/1eA9.5 kJ/m²3.0 kJ/m²25 kJ/m²
    Notched Charpy impact (0 °C)ISO 179-1/1eA3.8 kJ/m²1.2 kJ/m²8.0 kJ/m²
    Heat deflection temperature (0.45 MPa)ISO 75-2B72 °C95 °C65 °C
    Haze (2 mm thickness)ASTM D100312 %55 %Opaque

    When Multi-Cavity Hot-Runner Tools Demand Low Residence Time

    High-output operations with 32- or 64-cavity hot-runner systems place an extreme demand on melt stability. Exelene C2004 has been run continuously for 72-hour trials on a 96-cavity syringe barrel mould with valve-gated hot runners maintained at 235 °C, where the total melt path from screw tip to cavity exceeds 800 mm. Under these conditions, MFR drift measured on samples collected every 6 hours remained within ±0.2 g/10 min, provided the manifold channels were sized to maintain shear rates below 1.5 × 10³ s⁻¹. In contrast, a heterophasic copolymer of the same nominal flow exhibited a +1.2 g/10 min upward MFR migration over the same period, attributed to shear-induced breakdown of the ethylene-propylene rubber phase and subsequent viscosity collapse. The random copolymer’s single-phase melt structure eliminates that inconsistency, making C2004 the preferred candidate for multicavity medical and packaging tools where cavity-to-cavity weight variation must stay below 0.15 % relative standard deviation. Balancing residence time is particularly critical when regrind is re-introduced at levels above 20 %. Repeated heat histories in a random copolymer accelerate the loss of ethylene co-monomer protection against oxidation. At 30 % regrind addition, tensile elongation at break dropped from an original 400 % to 280 % after 5 cycles, measured according to ISO 527-2/1A. This deterioration is non-linear and must be factored into scrap management protocols. Amorphous phase density and gas permeability also distinguish random copolymers. Oxygen transmission rate through a 0.5 mm film of C2004 is approximately 1800 cm³/(m²·day·bar) at 23 °C and 0 % RH (ASTM D3985), roughly 8 % higher than through a homopolymer of equivalent thickness, a consequence of the expanded free volume in the ethylene-containing amorphous regions. While this marginal difference is immaterial in most packaging, it becomes a design factor when modifying barrier layer thickness in co-injection structures. Pigment dispersion in Exelene C2004 benefits from a slightly broader molecular weight distribution than earlier-generation random copolymers, as evidenced by a polydispersity index of approximately 4.8 measured via high-temperature GPC. This breadth enhances shear transfer in single-screw extruder mixing zones, enabling a 40:1 masterbatch letdown ratio with organic red pigments to achieve a Delta E colour uniformity below 0.8 (CIE L*a*b*, D65 illuminant) across a 16-cavity mould. Titanium dioxide additions up to 2 phr do not significantly nucleate the melt; crystallisation temperature (Tc) shifts by less than 2 °C as recorded by DSC cooling scans, preserving the clarity advantage over homopolymer where the same TiO₂ loading can raise Tc by 8–10 °C and induce haze. Regulatory compliance for food contact applications is anchored to Commission Regulation (EU) No 10/2011 and its subsequent amendments. Exelene C2004 formulated without intentionally added substances of very high concern (SVHC) meets the overall migration limit of 10 mg/dm² under simulant B (3 % acetic acid) and simulant D2 (vegetable oil) at 70 °C for 2 hours. For United States FDA clearance, the base polymer composition complies with 21 CFR §177.1520(c) items 1.1a and 3.2a, covering random copolymers for non-alcoholic food contact up to 100 °C depending on food type. A separate declaration for metal trace content following CONEG model legislation confirms lead, mercury, cadmium, and hexavalent chromium each below the 100 ppm sum threshold.
    Essential regulatory references and compliance status
    Standard / RegulationScopeStatus for Exelene C2004
    EU 10/2011 (consolidated)Plastics intended to come into contact with foodOverall migration <10 mg/dm²; positive-list monomers only
    FDA 21 CFR §177.1520Olefin polymersMeets (c) 1.1a and 3.2a; conditions of use A through H
    CONEG toxics in packagingHeavy metal limits (US)Sum Pb+Cd+Hg+Cr(VI) <100 ppm
    RoHS Directive 2011/65/EU (recast)Electrical and electronic equipmentNot within scope for mechanical components, but voluntarily meets Annex II restrictions
    USP Class VI (biological reactivity)Medical device plasticsExtraction test data available; meets systemic injection, intracutaneous, and implantation limits
    Mechanical durability in cold-chain logistics highlights a limitation. When containers filled with water are subjected to a 1.2 m drop test at -5 °C, the failure probability for C2004 rises to approximately 25 % compared to 5 % at 23 °C. This sensitivity restricts unmodified use in frozen-food packaging where impact resistance below -10 °C is specified; blending with an impact copolymer becomes necessary at additive levels of 15–20 %, though such blending inevitably sacrifices transparency. The upper service temperature in continuous load-bearing applications is capped at 55 °C due to creep modulus decay; tensile creep modulus at 1000 hours under 5 MPa static stress declines to 320 MPa, roughly 65 % of its initial value, as per ISO 899-1. Polyolefin welding and joining processes for C2004 align with standard spin-welding parameters: a weld velocity of 10 m/s and an axial pressure of 0.6 MPa for 1.5 seconds produce a weld factor of 0.85 compared to parent tensile strength. Ultrasonic welding at 20 kHz with an amplitude of 35 µm necessitates a joint design with a 60° energy director to compensate for the lower shear modulus relative to homopolymer. These joining parameters are routinely validated on production lines assembling laboratory pipette tips and centrifuge tube closures, where a coherent weld without particulate generation is non-negotiable.
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