| HS Code | 714604 |
| Density | 0.90 g/cm³ |
| Melt Flow Rate 230 C 2 16 Kg | 35 g/10 min |
| Tensile Strength At Yield | 25 MPa |
| Elongation At Break | 150 % |
| Flexural Modulus | 1150 MPa |
| Izod Impact Strength Notched 23 C | 5.0 kJ/m² |
| Heat Deflection Temperature 0 45 Mpa | 85 °C |
| Vicat Softening Temperature | 145 °C |
| Rockwell Hardness | R-85 |
| Melting Point | 160 °C |
| Mold Shrinkage | 1.3 % |
| Volume Resistivity | 1.0E+15 ohm·cm |
As an accredited MARPOL COPP 35.1.5 PP Copolymer factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | MARPOL COPP 35.1.5 PP Copolymer is supplied in 25 kg heat-sealed, polyethylene-lined paper bags, shrink-wrapped and palletized. |
| Container Loading (20′ FCL) | 20′ FCL: palletized PP copolymer bags loaded securely, weight-distributed, blocked and braced for safe, efficient container transport. |
| Shipping | Shipping description for MARPOL COPP 35.1.5 PP Copolymer: Polypropylene copolymer pellets, not regulated as dangerous goods under IMDG. Proper shipping name: Polypropylene Copolymer; UN No.: not applicable; marine pollutant: No; MARPOL Annex II: not applicable. Pack in clean, dry containers/bags; avoid moisture, heat, dust accumulation and static discharge. |
| Storage | Store MARPOL COPP 35.1.5 PP Copolymer in a cool, dry, well-ventilated area, protected from direct sunlight, moisture, and temperatures above specified limits. Keep original containers tightly sealed and away from open flames, strong oxidizers, or ignition sources. Avoid mechanical damage to packaging. No special storage required; maintain good housekeeping and segregation from incompatible materials. Ensure handling equipment is clean to prevent contamination. |
| Shelf Life | Shelf life is typically 12 months when stored sealed, cool, and dry, protected from sunlight, moisture, and contamination. |
Injection moulding of thin-wall automotive interior substrates with MARPOL COPP 35.1.5 PP Copolymer is controlled by the interaction of 35 g/10 min melt flow, shear-thinning behaviour, and slow crystallisation at the tool surface. The grade is processed in the melt-temperature band of 225 °C to 245 °C, with tool surface temperature maintained between 20 °C and 45 °C because lower tool temperatures elevate frozen-in orientation and increase the risk of gloss variation on grained surfaces. The nominal melt flow rate of 35 g/10 min at 230 °C under 2.16 kg load, determined by ISO 1133-1:2022, supports flow length/wall thickness ratios above 200:1 in multi-cavity tools equipped with sequential valve-gate control. Production-scale tools for door map pockets and glove box surrounds typically require clamp force in the range 0.5 ton/cm² to 0.7 ton/cm² of projected area, but the dominant process variable is not clamp force alone. Fill imbalance above 10 % is corrected through independent valve-gate opening delays rather than by increasing global melt temperature, because overheating produces visible flow-hesitation bands and local gloss reduction at rib intersections. Post-mould shrinkage measured on plaques conditioned for 24 h at 23 °C under ISO 294-4 generally falls between 1.2 % and 1.6 % in flow orientation and between 1.3 % and 1.7 % transverse to flow. The as-supplied stabilisation must be sufficient to allow volatile organic compound performance under VDA 277 and fogging behaviour under ISO 6452 for interior applications. A migratory hindered phenolic stabiliser content above 0.1 % by weight of the final part should be avoided because it elevates fogging condensate on glass surfaces. Pre-drying at 80 °C for 2 h is applied only when bulk moisture exceeds 0.05 %; field observations on automotive moulding lines show no meaningful improvement in knot line strength or surface quality below 0.03 % moisture. Terminal articles include A-pillar lower covers, door map pockets, glove box surrounds, load-floor trim wells, and scuff-plate substrates. The main failure modes are sink marks at bosses with a depth-to-part-thickness ratio above 0.6 and jetting at the gate when the gate diameter is below 0.8 mm without a fan or tab gate geometry.
Wall thickness reduction in injection-moulded PP copolymer pails is governed less by melt fluidity than by the interaction between cooling-rate-induced crystallinity gradients and low-temperature drop-impact resistance. MARPOL COPP 35.1.5 PP Copolymer with nominal 35 g/10 min MFR under ISO 1133-1:2022 at 230 °C/2.16 kg permits sidewall thickness down to 1.5 mm in tools with hot-runner multiple gates and accumulator-assisted fill times of 0.5 s to 0.9 s. At these fill speeds, the apparent viscosity in the high-flow impact copolymer class at 230 °C and 1000 s⁻¹ is commonly 90 Pa·s to 120 Pa·s, although published data for this exact MARPOL configuration is limited. Production trials on 20 L pail tools demonstrate that reducing sidewall below 1.4 mm shifts the limiting failure from drop impact at -18 °C to top-load buckling. Top-load compression is measured under ISO 12048, and the failure mode is frequently initiated at the gate land rather than in the sidewall. For UN-certified industrial pails, filled-container drop testing under ASTM D5276 at -18 °C requires leak-tight and breach-free performance after impact on seams, corners, and gate areas. The formulation should incorporate a hindered phenolic/phosphate antioxidant package at 0.12 wt% to 0.18 wt% and, for coloured pails, a masterbatch containing low-migration organic pigments at 2 wt% to 3 wt%. Tool temperature is maintained at 12 °C to 25 °C; lower tool temperatures reduce cycle time but increase frozen-in stress near the gate, which can appear as circumferential splitting after low-temperature drop testing. Terminal articles include 5 L to 25 L round and rectangular containers, tamper-evident lids, and open-top industrial pails. The practical wall-thickness floor is therefore established by the balance between drop impact and compressive buckling, not by spiral-flow length alone.
Twin-screw compounding of MARPOL COPP 35.1.5 PP Copolymer into talc- or glass-reinforced grades is performed on co-rotating twin-screw extruders with L/D 40:1 to 52:1 and specific torque ratings in the region of 8 N·m/cm³ to 11 N·m/cm³. Talc is side-fed at zone 4 or 5, while vacuum degassing is applied at zone 8 with a vacuum level of -0.08 MPa to -0.095 MPa. Melt temperature at the die is held between 210 °C and 230 °C, and screw speed is controlled at 400 rpm to 600 rpm. For talc loadings of 20 wt% to 40 wt%, the high-flow base resin permits filler incorporation without exceeding the torque limit, but the final melt flow rate drops from the nominal 35 g/10 min to 18 g/10 min to 28 g/10 min depending on filler level and screw configuration. For short glass fibre loadings of 10 wt% to 30 wt%, maleic anhydride grafted polypropylene is dosed at 1.5 wt% to 3.0 wt% of the total compound to maintain interfacial adhesion and prevent fibre pull-out under tensile loading. Reactive vis-breaking with organic peroxide at 0.02 wt% to 0.08 wt% is used only when the final compound must exceed 45 g/10 min for very thin-wall moulding, because peroxide-induced chain scission reduces low-temperature impact significantly. Pre-drying at 80 °C for 2 h is recommended when bulk moisture exceeds 0.05 %, and the vent port should be checked for fines accumulation when talc loadings exceed 35 wt%. The table below presents representative comparative data for unfilled and talc-filled high-flow PP impact copolymer compounds in the same melt-flow class; these values are drawn from published industrial compound data and are not a product specification for MARPOL COPP 35.1.5.
| Formulation | Talc content, wt% | Tensile yield strength, ISO 527-2, MPa | Flexural modulus, ISO 178, MPa | Notched Charpy impact at 23 °C, ISO 179-1/1eA, kJ/m² | MFR at 230 °C/2.16 kg, ISO 1133-1, g/10 min |
| Unfilled impact copolymer | 0 | 25 | 1300 | 8.0 | 35 |
| Talc-reinforced compound | 20 | 28 | 2200 | 5.0 | 28 |
| Talc-reinforced compound | 30 | 30 | 2800 | 4.0 | 20 |
| Talc-reinforced compound | 40 | 31 | 3500 | 3.5 | 18 |
The comparative data show that notched Charpy impact declines as talc content rises; therefore, impact-modified PP carrier resins with high initial ductility are preferred when talc loading exceeds 30 wt%. Compounds intended for automotive or appliance structural parts should be validated on the specific production line because barrel wear and screw configuration shift the balance between filler dispersion and matrix degradation.
When food-contact moulding falls under EU Regulation (EU) No 10/2011 and FDA 21 CFR 177.1520, the conversion route must exclude slip agents, antistatic additives, and mould-release sprays that are not listed for the intended food type. The base copolymer is processed at melt temperatures between 220 °C and 240 °C and tool temperatures between 15 °C and 35 °C; higher melt temperatures accelerate the formation of low-molecular-weight oxidation products that can raise overall migration values. For reusable kitchenware and storage containers, overall migration is measured on the finished article under EU Regulation (EU) No 10/2011 using food simulants A, B, C, D1 or D2 as appropriate, with the limit value of 10 mg/dm². Under FDA 21 CFR 177.1520, the olefin polymer must meet extraction limits for fatty and aqueous simulants and be manufactured under conditions that preserve the polymer identity specified in the regulation. Production-scale moulders should pre-dry the pellets at 80 °C for 2 h when storage relative humidity exceeds 60 %; otherwise hydrolysis of processing stabilisers is minimal and surface splay can be controlled by lowering back pressure to 5 bar to 10 bar. The use of purging compounds containing fluoropolymer processing aids should be avoided because their residues can interfere with food-contact compliance verification. Terminal articles include reusable food storage containers, kitchen appliance housings, and thin-wall food pails where the sealing surface must remain dimensionally stable after repeated dishwasher cycles at 65 °C. The compliance checklist below summarises the principal regulatory milestones for food-contact and general consumer articles based on this material class.
| Regulatory requirement | Standard or regulation | Typical limit or criterion |
| Overall migration | EU Regulation (EU) No 10/2011 | 10 mg/dm² |
| Olefin polymer extraction | FDA 21 CFR 177.1520 | Extraction limits per 21 CFR |
| Total migration for plastic food contact | GB 4806.7-2016 | 10 mg/dm² |
| Substances of very high concern | Regulation (EC) No 1907/2006 | 0.1 wt% per article |
The result of these constraints is that an unmodified high-flow PP copolymer can serve food-contact applications only when the additive package is selected from positive-list components and the thermal history remains within the range validated by migration testing.
Battery carrier and module holder compounds based on high-flow PP impact copolymer require a balance of low-temperature ductility, creep resistance under 85 °C continuous service, and flame-retardant behaviour. For non-flame-retarded structural carriers, MARPOL COPP 35.1.5 PP Copolymer may be compounded with 20 wt% to 30 wt% short glass fibre and 2 wt% to 4 wt% maleic anhydride grafted PP coupling agent; the coupling agent is dosed upstream of fibre side-feeding on a twin-screw extruder with L/D 44:1. When flame retardancy is required to UL 94 V-0 at 3.0 mm, an intumescent ammonium polyphosphate/pentaerythritol system is dispersed at 22 wt% to 28 wt% total loading, with the processing window limited to 190 °C to 220 °C to avoid pre-foaming at the die. The main processing conflict is that impact modifiers used to restore sub-zero ductility, typically ethylene-octene copolymers at 8 wt% to 15 wt%, reduce tensile modulus and can lower the heat deflection temperature under ISO 75-2. Therefore, the formulation is iterated through notched Charpy impact by ISO 179-1/1eA at -30 °C, flexural modulus by ISO 178, and flammability by IEC 60695-11-10 or UL 94. Regrind levels above 15 wt% in flame-retarded carriers are not recommended because repeated heating of intumescent FR systems increases melt viscosity and can cause gas evolution at the injection unit before the check ring seals. Terminal components include battery module side plates, busbar covers, and low-voltage connector brackets. Published data for this specific MARPOL grade in long-glass-fibre FR configurations is limited; the values given here are representative industrial starting points for the high-flow impact copolymer class and should be confirmed by compound qualification trials.
White-goods applications consume high-flow PP copolymer as a 20 wt% talc-filled compound for washing machine tubs, base frames, and pump housings where detergent resistance and creep stiffness at 60 °C are primary. The talc-filled compound is injection moulded in tools with projected areas above 0.8 m² using sequential valve-gate control and clamp force of 0.55 ton/cm² to 0.75 ton/cm²; melt temperature is held at 230 °C to 250 °C to maintain weld-line strength. In service, the part must meet abnormal-operation testing under IEC 60335-1 and maintain mechanical relative thermal index under UL 746B with a 90 °C mechanical RTI for talc-filled PP. The most common field failure is environmental stress cracking at weld lines exposed to alkaline detergent at 60 °C; this is reduced by increasing the mould temperature to 40 °C and relocating gates to place weld lines outside the primary hoop stress zone of the outer tub. Unfilled MARPOL COPP 35.1.5 PP Copolymer is not recommended for the outer tub because of insufficient hot-water creep modulus; the tub compound is typically produced by compounding 70 wt% of this resin with 20 wt% talc and 10 wt% impact modifier. Terminal articles include washing machine tubs, dryer bases, dishwasher inner frames, and refrigerator kick plates. Shrinkage values after 24 h under ISO 294-4 are typically 0.9 % to 1.2 % for the talc-filled compound, significantly lower than for unfilled high-flow PP and essential for matching dimensional tolerances across large sealing surfaces.
The same high-flow impact copolymer is used for injection-moulded returnable transit packaging in which drop-impact at -20 °C and repeated stacking are specified. For a standard 600 mm × 400 mm Euro crate, tool design uses multiple hot-runner nozzles and deep ribs with a wall thickness between 2.2 mm and 3.0 mm; the high MFR of 35 g/10 min permits fill from a central gate to the outer corners without exceeding a melt temperature of 240 °C. The formulation may include 2 wt% to 5 wt% high-density polyethylene or an ethylene-α-olefin impact modifier to lift notched impact at -20 °C above 6 kJ/m² when tested by ISO 179-1/1eA. For meat, dairy, and bakery distribution crates, material compliance is generally assessed under EU Regulation (EU) No 10/2011 for food contact or under FDA 21 CFR 177.1520; industrial crates require REACH compliance for substances of very high concern below 0.1 wt%. Production-scale observations show that dimensionally stable crates require low orientation shrinkage. Unfilled copolymer may exhibit post-mould shrinkage up to 1.7 %, so a nucleating agent at 0.05 wt% to 0.1 wt% is added to reduce anisotropic shrinkage and shorten cycle time. Terminal articles include ventilated fruit and vegetable crates, collapsible dairy crates, industrial pallet boxes, and refuse-bin bodies. The main limitation is low-temperature brittleness if regrind is reused above 30 wt%; repeated heat history reduces the ethylene-phase toughening effect and increases brittle failure in drop tests at -20 °C.
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Introduced as a polypropylene copolymer in the high-flow injection-molding segment, MARPOL COPP 35.1.5 is identified by a nominal melt mass-flow rate of 35 g/10 min when measured at 230°C under 2.16 kg in accordance with ISO 1133-1:2022. The “COPP” designation places the product in the ethylene-modified polypropylene class, while the 35.1.5 suffix is a producer-specific grade code denoting the nominal flow band and sub-formulation. It is primarily used for thin-wall rigid packaging, caps and closures, appliance interior components, and automotive inner carriers where reduced injection pressure and short cycle time are required. Because public certificate-of-analysis data for this exact grade is limited to direct supply documentation, the values in the following sections refer to the published envelope for polypropylene copolymers in the 30–40 g/10 min melt-flow band and should be confirmed against the producer’s lot release.
Processing is normally conducted on a hydraulic or electric injection-molding machine with a screw L/D of 20:1–24:1 and a compression ratio of 2.0:1–2.5:1. The recommended melt temperature is 220–250°C; for thin-wall cavities with flow length-to-thickness ratios exceeding 150:1, the melt-temperature setpoint is held at 230°C ±5°C. Below 225°C, the reduced melt fluidity increases cavity fill pressure and raises the probability of short shots; above 235°C in prolonged cycles, thermo-oxidative chain scission may shift the in-process melt flow by more than 5 g/10 min and create sink marks or gate blush. Mold temperature is generally maintained at 10–40°C, with the upper region preferred for high-gloss surfaces and the lower region for fast demolding of deep-draw parts.
Injection pressure for 1.0–1.5 mm wall thickness lies typically between 80–120 MPa, with holding pressure set to 60–80% of peak injection pressure. Clamp force requirements are typically 0.4–0.6 t/cm² of projected area. Screw recovery should be timed so that melt residence time at 240°C does not exceed 5 min; longer residence produces yellowing and a measurable reduction in notched Charpy impact. Moisture pickup is low, but if containers are stored at relative humidity above 60% or exposed to condensation, pre-drying with a desiccant dryer at 80°C for 2–4 h to a dew point of −30°C is applied before processing. Published capillary rheometry for high-flow polypropylene copolymers in this MFR band reports apparent viscosity in the 60–90 Pa·s range at 230°C and 1,000 s⁻¹, which supports thin-wall filling without excessive clamp force.
In production-scale thin-wall molding, two failure modes dominate when the processing window is not maintained. The first is gate blush caused by excessive shear heating at restricted gate diameters below 0.8 mm; the second is warpage caused by differential shrinkage between the flow direction and transverse direction. Shrinkage of the high-flow copolymer class is typically 1.2–1.6% in the flow direction and 1.0–1.4% in the transverse direction after 48 h at room temperature per ISO 294-4. Mold design therefore requires gate placement that avoids long unidirectional flow paths. On a 1,200 kN electric injection-molding machine, the fill time for a 0.8 mm wall part can fall below 0.4 s; gate freeze time is controlled by part geometry rather than material solidification because the copolymer has a broad crystallization exotherm.
Compared with a homopolymer grade of equivalent melt flow, MARPOL COPP 35.1.5 contains a controlled ethylene sequence that reduces crystallinity and increases the temperature range over which ductile deformation occurs. The trade-off is a lower tensile stiffness. Typical values for the copolymer class are a tensile yield stress of 25–28 MPa at 50 mm/min per ASTM D638-14, a tensile modulus of 1,100–1,300 MPa per ISO 527-2/1A, and a flexural modulus of 1,100–1,350 MPa per ISO 178. A homopolymer with the same MFR usually exhibits tensile yield stress above 30 MPa and flexural modulus above 1,400 MPa. Conversely, notched Charpy impact at 23°C for the high-flow copolymer envelope is reported in the 4–8 kJ/m² range per ISO 179-1/1eA, whereas a comparable homopolymer may drop below 2 kJ/m² at −20°C.
| Property | Test Method | PP Homopolymer | PP Random Copolymer | MARPOL COPP 35.1.5 Target Envelope |
|---|---|---|---|---|
| Melt flow rate | ISO 1133-1:2022 | 35 g/10 min | 35 g/10 min | 30–40 g/10 min |
| Tensile stress at yield | ASTM D638-14 | 30–34 MPa | 24–28 MPa | 25–28 MPa |
| Flexural modulus | ISO 178 | 1,400–1,700 MPa | 900–1,200 MPa | 1,100–1,350 MPa |
| Notched Charpy impact at 23°C | ISO 179-1/1eA | 2–4 kJ/m² | 3–6 kJ/m² | 4–8 kJ/m² |
| Notched Charpy impact at −20°C | ISO 179-1/1eA | 1–2 kJ/m² | 2–3 kJ/m² | 2–4 kJ/m² |
| Heat deflection temperature at 0.45 MPa | ISO 75-2 | 85–95°C | 70–80°C | 75–85°C |
The phase architecture of MARPOL COPP 35.1.5 is not disclosed in public documentation; in impact-copolymer grades, ethylene-propylene rubber domains are dispersed in a polypropylene matrix, and the ethylene content strongly controls the stiffness–impact balance. When ethylene content exceeds 3 wt%, the tensile modulus typically falls by 10–20% before the −20°C notched impact improves significantly. In random copolymers, ethylene is inserted in the polypropylene chain at 1–4 wt%, which primarily improves optical clarity and heat-seal initiation temperature but provides less low-temperature impact than a heterophasic impact copolymer. Users converting MARPOL COPP 35.1.5 should request the ethylene distribution type from the certificate of analysis because the selection between random and impact architecture changes weld-line strength, haze, and dimensional stability in ways that are not visible from melt flow rate alone.
Differential scanning calorimetry of the copolymer class per ISO 11357-3 generally shows a melting peak at 158–165°C; homopolymer peaks are typically 160–168°C. The lower melting endotherm and broader crystallization exotherm of copolymer grades can reduce cycle time in injection molding, but the same structural feature lowers the upper-use temperature under load. In weld-line regions, tensile strength retention should be measured rather than assumed; published data for high-flow PP copolymers indicates weld-line tensile strength retention of 70–85% relative to unwelded tensile bars per ASTM D638-14, with the higher retention observed at melt temperatures above 230°C and rapid injection speeds.
For appearance parts, the choice between a random copolymer and a heterophasic impact copolymer becomes visible in gate and weld-line regions. If the grade is an impact copolymer, its ethylene-propylene rubber phase raises haze at 1 mm thickness to 20–70% per ASTM D1003, while a random copolymer of the same MFR remains in the 5–15% haze range. This optical difference is one of the most reliable distinctions between MARPOL COPP 35.1.5 and lower-impact random grades during incoming inspection. The same rubber phase also reduces shrinkage anisotropy; mold shrinkage of a heterophasic grade tends to be more isotropic than that of a homopolymer, with transverse-to-flow shrinkage ratio of 0.8–0.9 versus 0.7–0.8 for homopolymer after 48 h.
On a 40:1 L/D co-rotating twin-screw extruder, MARPOL COPP 35.1.5 can be used as a dilution resin for masterbatch or as a carrier for mineral-filled compounds. The 35 g/10 min flow reduces pressure drop across the screen changer and die compared with a 12 g/10 min homopolymer carrier; die-pressure reductions of 3–5 MPa have been reported at 300 kg/h on a 75 mm machine. Batch-to-batch MFR variation of ±2 g/10 min can shift cavity fill pressure by 5–10% in thin-wall tools, which is why in-line rheological testing or capillary rheometry per ISO 11443 is recommended for incoming lots. If the product is compounded with glass fiber, coupling agents should be selected for polypropylene matrices, and the melt temperature should not exceed 220°C in the first barrel zones to prevent lubricant migration and die lip plate-out.
Long-term thermal aging under load should be verified for underhood or appliance applications. Unstabilized polypropylene copolymers of this class are not rated for sustained exposure above 90°C; properly stabilized grades can retain tensile properties after 1,000 h at 100°C per ISO 4577, but published data for this specific MARPOL grade is limited. Outdoor weathering without carbon black or hindered amine light stabilizers results in surface chalking within 6–12 months; 2 wt% carbon black masterbatch is the standard protection for outdoor PP articles. In UV-stabilized formulations, accelerated weathering per ISO 4892-2 is commonly used, but correlation to real-world endurance depends on climatic zone and part orientation.
In electrical enclosures and appliance interiors, the high-flow copolymer class typically exhibits volume resistivity above 1×10¹⁶ Ω·cm per IEC 62631-3-1, surface resistivity above 1×10¹⁴ Ω per IEC 62631-3-2, and dielectric strength of 25–35 kV/mm per IEC 60243-1. Comparative tracking index is usually 600 V per IEC 60112. These values support use in non-primary-insulation components, but the converter must verify final wall thickness and contamination because carbon-black or metal pigment loadings can lower surface resistivity by several orders of magnitude.
Incoming lot acceptance for MARPOL COPP 35.1.5 should include melt flow rate per ISO 1133-1:2022, ash content per ISO 3451-1, and notched Charpy impact per ISO 179-1/1eA. A frequency of once per 25,000 kg is common for automotive and appliance converters, while food-contact operations may perform melt-flow and organoleptic checks on every batch. Ash content above 0.05 wt% may indicate contamination or inconsistent additive dispersion and should trigger a filter pressure test before use.
Compliance statements cannot be transferred from a generic resin class to a specific grade without lot-level verification. For food-contact applications, the converter must confirm that the final article meets FDA 21 CFR 177.1520 olefin polymer conditions of use A through H and, for the European Union, Commission Regulation (EU) No 10/2011 with the applicable overall migration limit of 10 mg/dm² for general food-contact articles or 60 mg/kg for infant food. In electrical and electronic equipment, Directive 2011/65/EU RoHS restrictions apply to lead, mercury, cadmium, hexavalent chromium, PBB, and PBDE at the 0.1 wt% homogenous-material threshold, with cadmium at 0.01 wt%. REACH Regulation (EC) No 1907/2006 requires communication or notification when a candidate-list substance is present above 0.1 wt% in an article. Specific migration of low-molecular-weight oligomers and processing aids should be evaluated under the intended time-temperature conditions; published data for MARPOL COPP 35.1.5 in fatty-food simulants is limited, and users should request a declaration of compliance from the producer before food-contact use.
Where the application involves fatty food contact, specific migration testing is performed under olive oil or 95% ethanol simulants per EN 1186-2 and EN 13130-1; aqueous food contact uses 10% ethanol or 3% acetic acid according to the product type. Polypropylene homopolymers and copolymers are known for low water absorption and generally low specific migration, but residual peroxide decomposition products and catalyst-neutralizing additives can enter the food simulant if the polymerization and pelletization conditions are not controlled. The final article manufacturer remains responsible for demonstrating that the sum of specific migration limits in Commission Regulation (EU) No 10/2011 Annex I is not exceeded under worst intended conditions of time and temperature.
| Regulatory domain | Standard or test | Limit or condition | Verification responsibility |
|---|---|---|---|
| US food contact | FDA 21 CFR 177.1520 | Conditions of use A–H | Final article manufacturer |
| EU food contact | Commission Regulation (EU) No 10/2011 | 10 mg/dm² overall migration; 60 mg/kg for infant food | Final article manufacturer |
| REACH | Regulation (EC) No 1907/2006 | 0.1 wt% SVHC communication threshold in article | Importer/producer |
| RoHS | Directive 2011/65/EU | 0.1 wt% homogenous material; Cd 0.01 wt% | Electrical/electronic producer |
| Heavy metals in packaging | 94/62/EC | Sum of Pb, Cd, Hg, Cr(VI) ≤ 100 ppm | Packaging supplier |