| HS Code | 912278 |
| Density | 1.05 g/cm³ |
| Melt Flow Rate | 10 g/10 min at 230°C, 2.16 kg |
| Filler Content | 20% talc |
| Tensile Strength At Yield | 23 MPa |
| Elongation At Yield | 4% |
| Flexural Modulus | 2100 MPa |
| Izod Notched Impact Strength | 6 kJ/m² at 23°C |
| Charpy Notched Impact Strength | 25 kJ/m² at 23°C |
| Heat Deflection Temperature | 100°C at 0.45 MPa |
| Vicat Softening Temperature | 120°C (B50) |
| Hardness | 75 Shore D |
| Water Absorption | <0.1% |
| Mold Shrinkage | 1.0% |
As an accredited Scolefin CT 4210 PP Copolymer factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Scolefin CT 4210 PP Copolymer is supplied in 25 kg sealed polyethylene-lined bags, ensuring safe handling and protection. |
| Container Loading (20′ FCL) | 20′ FCL: 20-foot container loaded with Scolefin CT 4210 PP Copolymer in sealed bags, palletized and secured for safe transport. |
| Shipping | Scolefin CT 4210 PP Copolymer ships as non-hazardous pellets in sealed bags, bulk bags, or hopper trucks. Keep dry, avoid excessive heat and direct sunlight during transit. Use clean, covered transport equipment. Handle with care to prevent bag damage or contamination, and store in a cool, ventilated area. |
| Storage | Store Scolefin CT 4210 PP Copolymer in a cool, dry, well-ventilated area away from direct sunlight, heat, and ignition sources. Keep containers tightly closed to prevent moisture contamination and foreign matter. Store in original packaging on a clean, dry surface. Avoid prolonged high temperatures. Under these conditions, material stability and performance are maintained. |
| Shelf Life | Shelf life is typically 2 years from date of manufacture when stored in original, unopened packaging under dry, cool conditions. |
Inside automotive interior trim programs, the first technical screening of Scolefin CT 4210 PP copolymer occurs on injection moulding platforms with clamp force from 3000 kN to 8000 kN and hot-runner valve-gated tools producing lower door panel substrates, A-pillar covers and glovebox surrounds. Grade-specific melt flow rate must be verified by ISO 1133-1:2022 at 230 °C under 2.16 kg before switch-over position is locked, because lot-to-lot MFR drift in high-flow impact copolymers can alter cavity pressure by 10–15 % in long rib flows exceeding 150:1 flow-length-to-wall-thickness ratio. Short-shot failures concentrate in thin bosses and rib intersections when hydraulic injection speed falls below 80 mm/s; cavity pressure sensors installed behind the last-filled regions should record at least 350 bar before switch-over to hold pressure to keep sink marks outside textured show surfaces. Melt temperatures are typically held between 230 °C and 255 °C; the lower boundary is set by filling pressure and the upper boundary by volatile emission from hot-runner dead spots rather than by thermal stability of the resin alone. Mechanical evaluations follow ISO 527-2/1A for tensile modulus and yield stress, ISO 179-1/1eA for notched Charpy impact at 23 °C and −20 °C, and ISO 178 for flexural modulus. Interior emission requirements are checked with VDA 278:2011 thermal desorption analysis, VDA 277 total carbon emission, and ISO 6452 fogging. Where OEM specification ceilings are imposed, values below 150 µg/g VOC and 50 µg C/g total carbon are often referenced, but these thresholds are application-specific and must not be taken as grade guarantees. Grained surface retention after heat ageing is tested according to ISO 175 at 100 °C for 500 h; gloss loss in this test correlates with additive migration and must be compared against grain depth measured by surface profilometry. The absence of amine-based stabilizer by-products in the resin package should be confirmed before chemical cleaning of textured tool surfaces, because amine residues can react with chlorinated cleaning solvents and produce visible bloom on the next production run.
When the same grade is applied to microwaveable food containers with nominal wall stock between 0.45 mm and 0.80 mm, the limiting factor shifts from impact strength to pressure-limited filling in multi-cavity stack moulds. Stack tools with 8+8 or 16+16 cavities and valve-gate hot runners demand injection speeds from 150 mm/s to 300 mm/s; below this range the flow front cools below the no-flow temperature before reaching the cavity periphery and produces edge tears or incomplete lids. Capillary rheometry according to ISO 11443 should be used to avoid shear heating above 260 °C at apparent shear rates exceeding 1000 s⁻¹, because the thin wall creates higher shear than compact parts and may trigger local degradation at the gate despite moderate barrel setpoints. Melt temperature is usually set between 240 °C and 270 °C; the upper limit is constrained not only by odour development but also by dimensional variation caused by cooling time extension. Mould temperature control from 15 °C to 40 °C with turbulent flow in cooling channels is applied to freeze the gate quickly and reduce cycle time; however, cavity-to-cavity temperature variation above ±2 °C in the mould base increases warpage on round container bases and can exceed flatness tolerance after demoulding. Food contact compliance requires migration testing on the finished article under EU 10/2011 with overall migration according to EN 1186-1 and specific migration according to EN 13130-1; for United States submissions, the supply-chain documentation should list 21 CFR 177.1520 for olefin polymers. Sensory panel evaluation under DIN 10955 is recommended when the container is used for fatty foods above 100 °C because microwave reheating accelerates odour release. Published data for this specific grade in stack-moulded containers with wall thickness below 0.5 mm is limited; trials should include a full factorial of injection speed, melt temperature and hold pressure to map the process window before commissioning.
| Conversion | Equipment configuration | Melt temperature range | Mould temperature | Key test standard |
|---|---|---|---|---|
| Automotive interior trim injection moulding | Clamp force 3000–8000 kN, hot runner | 230–255 °C | 30–60 °C | ISO 527-2/1A, ISO 179-1/1eA |
| Thin-wall packaging stack mould | 8+8 cavity stack, valve gate | 240–270 °C | 15–40 °C | ISO 1133-1:2022, ISO 11443 |
| High-cavity closure moulding | 64/96 cavity, hot runner | 220–250 °C | 10–25 °C | ASTM D3198-21, ISO 179-1/1eA |
| Large appliance structural moulding | Sequential valve gating | 230–250 °C | 20–50 °C | ISO 175, ISO 899-1 |
The above table lists indicative reference ranges for PP impact copolymer conversion, not product-specific specifications; every lot must be validated on the target tool.
Closure moulding for carbonated soft drink and mineral water bottles is a downstream application where the copolymer is converted on high-cavity tools of 64 or 96 cavities with hot-runner valve pin systems and cycle times below 5 seconds. The material is fed through screw diameters of 40 mm to 60 mm with high compression ratios; melt temperature is typically held between 220 °C and 250 °C to limit acetaldehyde generation and preserve the performance of acid-scavenging additives. Injection speed is kept deliberately moderate rather than extreme because high shear at the valve gate can break the oriented skin layer and cause gate blush on the closure top surface. Removal torque and application torque are measured on a torque meter according to ASTM D3198-21 after the closure has been conditioned at 23 °C and 50 % relative humidity for 24 h. Loss of torque retention in carbonated beverage closures is linked to creep of the closure thread root and liner compression set, not only to material modulus; therefore ISO 899-1 tensile creep and ISO 34-1 tear strength are also relevant when a linerless seal is used. Carbon dioxide pressure inside the package produces sustained hoop stress on the closure skirt; stress crack resistance in contact with sodium dodecyl sulfate at 50 °C is used by some beverage producers as a screening test but published data specific to this configuration is limited. Organoleptic neutrality is verified after this stress crack test rather than only on virgin pellets because stress cracking can expose internal unstabilised polymer surfaces. The closure thread design must avoid sharp notches below 0.2 mm radius; production-scale failure analyses show that thread roots are the primary initiation points for environmental stress cracking under carbonation pressure cycling from 0 bar to 7 bar at 4 °C to 40 °C. Siloxane-based mould release agents should not be used on closure threads without validation because they interfere with print adhesion on the closure shell and can reduce slip additive migration consistency.
In large appliance structural parts, Scolefin CT 4210 PP copolymer is processed on injection moulding machines with clamp force from 8000 kN to 16000 kN and shot capacities above 3000 g. Sequential valve gating is used on washing machine outer tubs to avoid weld lines at the bearing carrier interface; gate opening is timed by cavity pressure sensors to maintain a flow front velocity above 120 mm/s through the last 20 % of fill. Melt temperature is set between 230 °C and 250 °C; mould temperature is held between 30 °C and 60 °C because higher mould temperature improves impact retention in thick sections but extends cooling time. Long-term behaviour in detergent solution is evaluated according to ISO 175 at 80 °C for 1000 h; tensile strength retention after immersion is measured by ISO 527-2/1A and notched Charpy impact retention by ISO 179-1/1eA at 23 °C. Creep performance of the tub under spin-cycle imbalance is assessed with ISO 899-1 at 80 °C; the material must not show total strain above a level that would allow the bearing carrier to shift during service. Pump housings exposed to chlorinated detergent and hot water require additional stress crack screening because hypochlorite solutions at 5 % concentration can initiate surface crazing in PP copolymers under sustained assembly stress. Published data for Scolefin CT 4210 in continuous hot-water contact above 90 °C remains limited; therefore validation under the intended detergent formulation is required before release. The electrical safety requirement for insulation parts is not automatically met by the base resin grade; relative thermal index values from UL 746B must be obtained from the supplier and applied only to the actual colour and additive package.
Medical diagnostic consumables manufactured from this copolymer include test tube racks, microcentrifuge tube holders and reaction vessel housings where dimensional stability after repeated autoclaving is more important than transparency. The material is converted on dedicated medical moulding machines with all-stainless steel barrels and screw surfaces to avoid cross-contamination from prior polyolefin production. Melt temperature is maintained between 220 °C and 260 °C; hot runner systems are required to have no dead spots because degraded resin can release particles into the finished article. Biocompatibility evaluation follows ISO 10993-5:2009 for cytotoxicity and ISO 10993-10:2010 for skin irritation and sensitisation; the testing is performed on the final sterilized article because autoclaving at 121 °C for 15 minutes can alter the low-molecular-weight extractable profile. Gamma irradiation at doses up to 25 kGy is commonly validated under ISO 11137-1, but doses above 25 kGy may shift tensile elongation and increase yellowness index measured according to ASTM E313. Ethylene oxide sterilisation requires aeration cycles to reduce residues; the part geometry should avoid blind holes and thick sections because EO retention in PP is higher than in amorphous polymers. Mould release agents are excluded from tooling used for medical components unless the specific release chemistry is included in the ISO 10993 extractables assessment. Dimensional stability after repeated steam sterilization is checked by measuring critical dimensions after 100 cycles at 121 °C; warpage in tall rack structures can exceed 1 mm if holding pressure is not optimized to compensate for post-moulding crystallisation shrinkage. Published data for this specific grade in irradiation-resistant medical applications is limited; qualification must include infrared spectroscopy of the post-irradiation surface because oxidative chain scission can increase carbonyl index and shift yellowness index.
| Application area | Regulatory framework | Test method | Measured parameter |
|---|---|---|---|
| Food contact packaging | EU 10/2011, 21 CFR 177.1520 | EN 1186-1, EN 13130-1 | Overall and specific migration |
| Automotive interior | OEM specification | VDA 278:2011, VDA 277, ISO 6452 | VOC, total carbon, fogging condensate |
| Medical consumables | ISO 10993-5:2009, ISO 10993-10:2010 | Extraction and cytotoxicity | Cell viability, skin irritation |
| Closures | Producer-specific | ASTM D3198-21 | Application and removal torque |
Compounding operations use Scolefin CT 4210 PP copolymer as the base resin for talc-filled and impact-modified formulations because the copolymer phase provides toughness retention after mineral addition lowers tensile elongation. The line configuration is typically a co-rotating twin-screw extruder with L/D 32:1 to 44:1, segmented screws, side stuffer at barrel 6 or 8, atmospheric vent upstream and vacuum vent downstream. Talc at 10–30 wt% is introduced through the side stuffer after the polymer has reached melt temperature between 190 °C and 220 °C; addition above 30 wt% raises melt pressure and may require the side stuffer to be repositioned or a second side feed zone to be used. Elastomer masterbatches with EPR or EPDM are added via the main feeder or side feeder depending on the masterbatch melt index; a viscosity ratio between the elastomer and PP copolymer below 3:1 at 100 s⁻¹ is recommended to prevent large rubber domains that reduce notched Charpy impact at −20 °C. Dispersive mixing elements are more critical than distributive elements when talc agglomerates are present; screw designs with 30–40 % of the process length dedicated to kneading blocks can achieve acceptable dispersion, but exact element arrangement must be validated on the specific line. Published data for this grade in compounds with talc above 40 wt% or with peroxide-initiated viscosity modification is limited; bench-scale mixing studies should precede production qualification because the thermal history in the extruder affects residual stabilizer concentration and long-term heat ageing according to ISO 75-2. Amine-based stabilizer packages should not be substituted into peroxide-containing formulations without preliminary testing, because premature crosslinking can occur and reduce melt flow rate measured by ISO 1133-1:2022 to values below the injection moulding target. The compounded pellet is then re-extruded or injection moulded into automotive and appliance articles; therefore pellet shape, bulk density and additive dispersion must be checked on a lot-by-lot basis using ISO 1133-1:2022 for melt flow rate, ISO 1183-1:2019 for density, and ISO 3451-1:2019 for filler content.
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Scolefin CT 4210 PP Copolymer is a polypropylene-based copolymer grade supplied in pellet form for injection moulding and related thermoplastic conversion processes. The CT 4210 designation places the material within the PP copolymer family, but it is not a homopolymer and should be distinguished from random copolymer PP by comonomer distribution, morphology, and resulting mechanical profile. No public lot-specific datasheet for this exact grade was identified at the time of writing; the processing windows and property envelopes given below are compound-class reference data and must be confirmed against the supplier’s certificate of analysis. Base characterisation is performed under ISO 1133-1:2022 for melt volume-flow rate at 230 °C/2.16 kg, ISO 1183-1:2019 for density, and ASTM D638-14 for tensile stress-strain response.
The material is specified where a balance of low-temperature impact energy absorption, mould release, and dimensional stability is required. In standard injection-moulded specimens, unfilled PP homopolymer typically exhibits notched Izod impact at 23 °C below 3 kJ/m² under ISO 180:2019/A, while impact-modified PP copolymers may exceed 10 kJ/m². The trade-off is stiffness: unfilled impact PP copolymers commonly show flexural modulus in the range of 1000–1600 MPa under ISO 178:2019, whereas general-purpose PP homopolymer often falls between 1500–1900 MPa. CT 4210 should therefore be evaluated within the impact-copolymer service envelope rather than the high-stiffness homopolymer envelope unless the certificate of analysis states otherwise.
For PP copolymer grades of the CT 4210 class, melt temperature is preferably maintained at 220–250 °C measured at the nozzle. A general-purpose screw with 20:1 L/D to 24:1 L/D is normally adequate, with a feed zone set at 200–210 °C, a compression zone at 220–240 °C, and a metering zone at 230–250 °C. Back pressure of 5–15 bar is applied to homogenise melt temperature and stabilise screw return. Screw speed on 35 mm to 60 mm screw diameters is typically 80–150 min⁻¹; higher speeds can reduce cycle time, but sustained melt temperature above 260 °C increases thermal-oxidative chain scission in PP copolymers and should be avoided.
Mould surface temperature is a threshold parameter because cooling rate influences skin-core morphology and low-temperature impact retention. For thin-wall parts below 1.5 mm, a mould surface temperature of 30–50 °C is commonly specified. Temperatures below 20 °C can suppress crystalline structures that contribute to post-mould toughness, while temperatures above 60 °C increase cycle time and may worsen ejection distortion. Drying is required only when moisture content exceeds 0.05% w/w or when regrind is present; sealed virgin PP copolymer pellets typically do not require pre-drying. If drying is required, 80 °C for 2–4 h in a desiccant dryer is a standard starting condition.
Gate velocity, not injection pressure alone, controls surface appearance and warpage in hot-runner multicavity tools. Published processing guides for PP copolymers recommend flow-front velocities of 100–300 mm/s in 1.5 mm wall sections. Velocities below this band can generate hesitation lines, while sustained velocities above 400 mm/s may induce jetting at the gate. Clamp force for thin-wall packaging should be calculated on a projected cavity area basis of 0.6–0.9 t/cm², but exact tonnage must account for gate freeze, pack pressure, and shrinkage anisotropy. Process simulation using pressure-volume-temperature data for the exact grade is recommended for parts with living hinges, snap features, or long flow-length-to-wall-thickness ratios.
Capillary rheometry under ISO 11443:2021 is used to establish shear-thinning behaviour. For unfilled impact PP copolymers at 230 °C, apparent viscosity at 1000 s⁻¹ is commonly in the range of 25–50 Pa·s, decreasing from 120–180 Pa·s at 100 s⁻¹. The shear-thinning ratio between 100 s⁻¹ and 1000 s⁻¹ is therefore approximately 3:1 to 5:1. CT 4210 should be assessed in a twin-bore capillary rheometer with a 1 mm die and 20:1 length-to-diameter ratio; Bagley and Rabinowitsch corrections are necessary to derive true shear stress and shear rate from pressure drop. Lot-to-lot variation in melt flow rate greater than ±1 g/10 min from the supplier’s nominal value can shift filling pressure by 10–15% in thin-wall applications. Incoming resin lots should therefore be checked under ISO 1133-1:2022 at 230 °C/2.16 kg before release to production.
The morphological origin of the property shift is the presence of ethylene-propylene rubber domains in heterophasic impact copolymers. These domains reduce stiffness relative to homopolymer but increase energy absorption through cavitation and shear yielding. For Scolefin CT 4210, impact data alone should not be used to infer chemical resistance, hardness, or barrier performance; the exact end-use property profile must be measured on specimens moulded under production cooling conditions because skin-core morphology in PP copolymers is extremely sensitive to thermal history.
| Property and method | PP homopolymer typical envelope | Random PP copolymer typical envelope | Impact PP copolymer class envelope |
|---|---|---|---|
| Flexural modulus under ISO 178:2019 (MPa) | 1500–1900 | 800–1200 | 1000–1600 |
| Notched Izod at 23 °C under ISO 180:2019/A (kJ/m²) | 2–4 | 4–8 | 10–30 |
| Tensile yield stress under ASTM D638-14 at 50 mm/min (MPa) | 30–37 | 22–30 | 18–28 |
| Elongation at break under ASTM D638-14 (%) | 20–150 | 200–500 | 50–400 |
| Heat deflection temperature B under ISO 75-2:2013 at 0.45 MPa (°C) | 85–105 | 70–90 | 70–100 |
Differences between Scolefin CT 4210 and alternative PP grades become visible primarily at low temperature and under high-speed loading. PP homopolymer provides higher modulus and better creep resistance but shows a ductile-to-brittle transition near 0–10 °C. Random PP copolymer improves optical clarity and reduces processing stress, but its notched impact at sub-zero temperatures is typically lower than that of a heterophasic impact copolymer. If CT 4210 is formulated as an impact-modified grade, it should be compared against other impact PP copolymers using notched Charpy under ISO 179-1:2010 at -20 °C and -40 °C, not only at ambient temperature. Published data for this specific configuration are limited; converters should request from the supplier the full ISO test dataset for tensile, flexural, Charpy, and Izod specimens.
Tool compatibility must be evaluated before substitution because unfilled impact PP copolymers shrink differently from talc-filled homopolymer. Talc-filled PP compounds often show machine-direction shrinkage of 0.8–1.0% under ISO 294-4:2018, whereas unfilled PP copolymers commonly shrink 1.2–1.8% depending on flow direction and nucleation. If Scolefin CT 4210 PP Copolymer is unfilled, the moulded dimensions may be smaller than those produced by a talc-filled homopolymer unless the cavity is recut or processing conditions are adjusted. The compensation is not linear because anisotropic shrinkage in an unfilled PP copolymer can differ by 0.3–0.6% between flow and cross-flow directions.
The substitution is not appropriate in high-stiffness structural brackets where talc-filled homopolymer provides flexural modulus above 2500 MPa. An unfilled impact PP copolymer rarely exceeds 1600 MPa in flexural modulus, so a stiffness deficit greater than 30% can produce service deflection exceeding 1 mm in loaded cantilever features even when low-temperature impact performance improves. Pack pressure and gate seal time must be recalculated because the softer grade may require longer packing to reduce sink marks and maintain dimensional capability in ribbed sections. A screw with compression ratio 2.5:1 to 3:1 is generally suitable; high-compression screws above 3.5:1 may over-shear the elastomeric phase and reduce impact retention.
Observed production-scale failure modes in PP impact copolymer processing include gate blush, tiger striping, and post-mould dimensional drift. Gate blush occurs in hot-runner systems when gate diameter is below 0.8 mm at high injection rate; increasing gate diameter to 1.0–1.5 mm or reducing initial fill speed is the standard correction. Tiger striping is associated with unstable flow-front velocity and can be mitigated by adjusting melt temperature in narrow 5 °C bands rather than by broad shifts outside the supplier’s window. Post-mould dimensional drift in unreinforced PP copolymer is driven by secondary crystallisation; parts should be conditioned at 23 °C and 50% relative humidity for 48 h under ISO 291:2008 before dimensional acceptance.
Regulatory status must be confirmed with product-specific declarations. For food-contact use, FDA 21 CFR 177.1520 covers olefin polymers and establishes conditions based on extractable fractions and intended food type. In the European Union, EU 10/2011 applies with an overall migration limit of 10 mg/dm². Under RoHS 2011/65/EU as amended by (EU) 2015/863, the homogeneous material thresholds are 1000 mg/kg for lead, 1000 mg/kg for mercury, 100 mg/kg for cadmium, and 1000 mg/kg for hexavalent chromium. REACH Candidate List substances must remain below 0.1% w/w per article. Additive masterbatches can alter regulatory status, so Scolefin CT 4210 should be assessed in the final compounded form used for the moulded article.
| Jurisdiction | Reference | Limits and notes |
|---|---|---|
| United States food contact | FDA 21 CFR 177.1520 | Compliance depends on extractable fractions and end-use food type. |
| European plastics food contact | EU 10/2011 | Overall migration 10 mg/dm²; substance-specific conditions apply. |
| EU hazardous substances | RoHS 2011/65/EU | Pb 1000 mg/kg, Hg 1000 mg/kg, Cd 100 mg/kg, Cr(VI) 1000 mg/kg. |
| REACH SVHC | Candidate List | Threshold 0.1% w/w per article. |