| HS Code | 445921 |
| Density | 0.9 g/cm³ |
| Melt Flow Rate | 5 g/10 min (230°C / 2.16 kg) |
| Tensile Strength At Yield | 30 MPa |
| Elongation At Break | 50% |
| Flexural Modulus | 900 MPa |
| Izod Notched Impact Strength 23c | 5 kJ/m² |
| Heat Deflection Temperature 0 45mpa | 85 °C |
| Vicat Softening Temperature | 130 °C |
| Melting Temperature | 145 °C |
| Haze | 10% |
As an accredited Symbios PP Terpolymer 4T05 factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Symbios PP Terpolymer 4T05 is supplied as pellets in 25 kg sealed bags, ensuring product purity and safe handling. |
| Container Loading (20′ FCL) | 20′ FCL container loading of Symbios PP Terpolymer 4T05 ensures secure, efficient transport, maximizing capacity and protecting product integrity during shipment. |
| Shipping | Symbios PP Terpolymer 4T05 is shipped as solid thermoplastic pellets in sealed polyethylene bags, typically 25 kg net each, packed on pallets with stretch film. It is non-hazardous under transport regulations, requiring dry, covered conditions to prevent moisture absorption and contamination during transit. |
| Storage | Store Symbios PP Terpolymer 4T05 in a cool, dry, well-ventilated area away from direct sunlight, heat sources, and ignition sources. Keep containers tightly sealed to prevent contamination and moisture absorption. Avoid contact with strong oxidizing agents. Maintain temperatures below 50°C and follow local regulations for polymer storage. |
| Shelf Life | Shelf life is typically 2 years from manufacture when stored in original sealed packaging in a cool, dry place. |
Three-layer cast film lines running symmetrical ABC coextruded structures with a 15–20% Symbios PP Terpolymer 4T05 sealant skin, a polypropylene homopolymer core, and a 15–20% 4T05 opposite skin are used for heat-seal packaging where the primary failure mode is seal initiation delay caused by heat soak through the core layer. The skin layer is processed at a melt temperature of 225–235°C, the core extruder at 230–245°C, and the feedblock and die at 235–240°C; a chill roll inlet temperature of 18–22°C is maintained to limit post-crystallisation haze. The layer ratio is critical because a sealant skin below 8 µm in total structure thickness can produce inconsistent seal strength under ASTM F88/F88M-21 due to substrate heat dissipation, while a skin above 20% of the total thickness reduces the flexural stiffness of the finished laminate. Seal initiation temperature is evaluated on a gradient heat sealer per ASTM F2029-16(2021) at a jaw pressure of 0.14 MPa and a 0.5 s dwell, and the characteristic heat seal range for C2/C3/C4 polypropylene terpolymers usually falls between 105°C and 120°C unless the supplier data sheet indicates otherwise. In food contact use, the sealant layer must comply with FDA 21 CFR 177.1520 for polyolefin polymers, Commission Regulation EU No 10/2011 with overall migration not exceeding 10 mg/dm² for the article contact layer, and specific migration verification for the slip and antiblock additives used in the formulation. A customary formulation modification is the addition of 3–5 wt% synthetic silica antiblock masterbatch and 500–1,000 ppm erucamide slip, but the exact migration limits under EU No 10/2011 require a specific migration test conducted on the finished structure, not on the pellet alone. Finished articles produced from this structure include flow wrap for bakery goods, lidding films for dairy cups, overwrap for optical media packaging, and polyethylene-free paper lamination films where the lower heat seal initiation temperature reduces sealing station energy input on horizontal form-fill-seal lines. The operational boundary is defined by the hot-tack window: above 85–90°C sealing bar temperature the web may become dimensionally unstable at high line speeds, and the structure is not recommended for hot-fill applications above 85°C or retort sterilization because the low melting point of the terpolymer skin leads to creep and seal failure under load.
The melt curtain in a high-speed extrusion coating line processing a 12 µm metallised PET substrate is oxidised by ozone injection in the air gap to increase the polar surface energy of a polypropylene terpolymer coating; without this step, peel adhesion to the metal layer can fall below 1.0 N/15 mm under the conditions of ISO 8510-2 90° peel testing. 4T05 is extruded through a coat hanger die at a coating weight of 12–20 g/m², with a melt temperature of 285–310°C and a line speed of 150–250 m/min, while the substrate is corona pre-treated to a minimum surface energy of 42–46 mN/m before entering the nip. The laid down coating is cooled on a matte finish cooling roll at 15–20°C and transferred between a pressure roll and a water-cooled back-up roll, with nip pressure adjusted to avoid metallised layer cracking. The lower melting enthalpy of a terpolymer compared to polypropylene homopolymer, measured by differential scanning calorimetry per ISO 11357-3, permits a narrower web-temperature control band at the die lip; a temperature excursion above 320°C can generate carbonyl degradation products that reduce seal strength and shift the odour profile of the finished laminate. In some operations, up to 20 wt% low-density polyethylene is introduced to improve adhesion and reduce draw resonance, but for all polyolefin food-contact layers the final coating must comply with FDA 21 CFR 177.1520 and EU No 10/2011, and the converter must verify overall migration on the complete laminate, not only on the coating resin. The terminal structures are used for stand-up pouch outer webs, confectionery sachets, coffee stick-pack laminates, and soap wrappers, where the terpolymer coating functions as both the sealing medium and the moisture barrier anchor. The limiting operational condition is the heat-sensitive substrate: metallised PET cannot tolerate prolonged tension above 120 N/m at the unwind station without microcracking, and the coating weight must be kept above 12 g/m² to avoid pinhole defect rates exceeding 0.1% under a 5 kV spark test.
At a transverse direction orientation ratio of 3.5:1, the shrink force generated by a 45 µm monolayer containing 4T05 is evaluated after biaxial stretching on a double-bubble line with a 55 mm single-screw extruder and a die gap of 0.8 mm. Melt temperature is held at 190–205°C, the first bubble is quenched at 8–12°C, and the second bubble is expanded at a reheating air temperature of 120–140°C before being collapsed and annealed in-line at 70–80°C for 5–8 s to stabilise shrink behaviour. The resin is blended with 15–25 wt% metallocene polyethylene or linear low-density polyethylene to reduce brittleness along the machine direction and to prevent stress-whitening in the folded edge; published data for this specific configuration with 4T05 is limited, so the blend ratio must be established by shrink-curve measurement rather than by extrapolation from homopolymer data. Free shrink is measured according to ASTM D2732-14 at 95°C and 105°C, and the shrinkage in the transverse direction must remain uniform within ±1.5 percentage points across the web to avoid label distortion during steam-tunnel shrinking at 85–95°C. The polymer layer used on food contact shrink labels must meet the requirements of Regulation EC No 1935/2004, Commission Regulation EU No 10/2011, and, for coloured labels, the specific migration limits of the pigments must be verified under the final article test conditions. The finished products are tamper-evident bands for beverage closures, full-body shrink sleeves for cosmetic bottles, and multipack collation film, all of which rely on the lower initiation temperature of the terpolymer to achieve complete recovery before the container surface reaches 70°C. The material is not recommended for storage in unventilated containers above 40°C because preshrinkage can begin before labelling, and exposure to high humidity above 80% RH can generate surface condensation that disrupts seaming on high-speed sleeve applicators.
A 0.8 mm diameter sprue and a cold runner with a 0.6 mm gate restrict the injection rate in an eight-cavity thin-wall container tool; the 4T05 melt temperature is set at 220–235°C, the mould coolant inlet is maintained at 10–18°C, and the injection pressure is kept between 35 MPa and 50 MPa to avoid flash while filling a 0.7 mm wall section. The lower crystallisation rate of a terpolymer permits longer flow in thin sections, but it also reduces the ejection modulus at a mould temperature above 30°C, so the cooling time is increased by 1.5–2.0 s relative to a polypropylene homopolymer of the same melt flow rate under ISO 1133-1:2022. The resulting parts are tested for haze by ASTM D1003, for tensile yield stress by ISO 527-2, and for notched Charpy impact at -20°C by ISO 179-1/1eA; expected values depend on the comonomer content and must be taken from the supplier certificate rather than inferred from the grade name. When 4T05 is blended with a 0.8 g/10 min polypropylene homopolymer for a beverage cap, a 20 wt% terpolymer fraction improves low-temperature impact on carbonated soft drink lines, but top-load strength after carbonation storage at 38°C under 2.5 volumes CO2 usually decreases because the terpolymer has a lower flexural modulus; cap manufacturers therefore select the blend ratio on a closure-specific basis, with top-load measured on a universal testing machine at 23°C using a 50 mm/min crosshead speed. For food contact caps and containers, the formulation must comply with FDA 21 CFR 177.1520, EU No 10/2011, and any applicable national provisions for organoleptic neutrality, and the use of colourants is restricted to those with positive list approval. The terminal articles include transparent caps for personal care bottles, thin-wall vials for non-sterile cosmetic powders, and overcaps for aerosol cans. The material is not suitable for retortable containers above 121°C, and the use temperature is limited to below 85°C under continuous load because creep resistance at elevated temperature is lower than that of a polypropylene homopolymer.
After exposure to 25 kGy absorbed dose in a cobalt-60 gamma source, sealant layers based on 4T05 may exhibit a measurable shift in low-temperature peel strength because ionising radiation oxidises the amorphous phase of the terpolymer and changes the fracture mode from interfacial peel to tear. The medical packaging structure is produced by extrusion lamination of a 30 µm 4T05 film onto a 12 µm polyester/9 µm aluminium foil laminate at a coating weight of 15 g/m², and the sealant side is sealed against an uncoated medical-grade paper web at 115–125°C, 0.28 MPa jaw pressure, and 0.5–1.0 s dwell. Seal strength before and after sterilisation is tested according to ASTM F88/F88M-21, and the leak integrity of the finished pouch is verified by ASTM F1929-12 dye penetration testing or ASTM F2338-09 vacuum decay; the packaging system must meet ISO 11607-1:2019 for terminally sterilised medical devices and ISO 10993-5:2009 for cytotoxicity if the pouch contact layer is claimed as a medical device material. The terpolymer’s lower melting point reduces the risk of fibre tear on medical paper at sealing temperatures above 120°C, but the post-sterilisation ageing margin must be validated at the final sealant thickness because thickness variations below 25 µm can shift peel strength by more than 0.5 N/15 mm.
| Compliance or Test Dimension | Reference Standard | Test Condition or Limiting Requirement |
|---|---|---|
| Seal strength | ASTM F88/F88M-21 | 15 mm width, 200–300 mm/min jaw separation |
| Heat sealability | ASTM F2029-16(2021) | 0.14 MPa pressure, 0.5 s dwell |
| Whole package leak | ASTM F1929-12 | Dye penetration, 20 min minimum |
| Vacuum decay | ASTM F2338-09 | Vacuum level control ±0.01 bar |
| Medical packaging system | ISO 11607-1:2019 | Sterile barrier validation, ageing |
| Cytotoxicity | ISO 10993-5:2009 | MEM elution, 72 h contact |
The terminal products include pouches for syringes, wound care dressings, and single-use tubing kits, but the material is not recommended for steam sterilisation above 121°C or for use as the only sterile barrier in high-humidity distribution environments without a secondary pouch.
Co-rotating twin-screw extruders with a 25:1 L/D ratio and vacuum devolatilisation at ≤50 mbar are used to produce a 40 wt% phthalocyanine blue masterbatch in a 4T05 carrier; the temperature profile is set at 150–190°C because the lower melting point of the carrier reduces thermal history on the pigment. The screw configuration employs two kneading blocks with 45° staggering and a reverse-screw element after the vent port to allow atmospheric venting before vacuum extraction; this reduces volatile residues and maintains pigment dispersion below a screen pack differential pressure of 0.3 MPa. The batch-to-batch control is performed by measuring the sieve residue after extrusion according to DIN EN 13900-5, and the carrier viscosity is checked by ISO 1133-1:2022 at 230°C with a 2.16 kg load. Finished masterbatch is used in polypropylene film and injection moulding lines at a let-down ratio of 2–5 wt%, with the final article colour concentrated enough to require no additional carrier during dry-blend tumbling. For toy applications, the masterbatch must be tested against the specific element migration limits of EN 71-3, and for electrical packaging the final product must comply with the RoHS Directive 2011/65/EU; REACH Regulation EC No 1907/2006, Annex XVII restrictions apply to certain pigments and processing aids. The terminal products are colour masterbatch for polypropylene caps, stationery clips, and non-food packaging containers, but the carrier alone does not confer food-contact approval unless all colorants and additives in the let-down meet the positive list of EU No 10/2011. Moisture uptake is typically below 0.05% under normal storage, but after exposure to relative humidity above 60% for more than 24 h, the pellets should be pre-dried at 60°C for 1–2 h to avoid surface moisture feeding into the vacuum vent.
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Symbios PP Terpolymer 4T05 is a propylene-based terpolymer grade incorporating ethylene and 1-butene as comonomers to depress crystallinity and reduce heat-seal initiation temperature relative to polypropylene homopolymers and propylene–ethylene random copolymers. The model designation 4T05 places the material in the low-to-mid melt-flow class; the final two digits are consistent with a nominal melt flow rate of 5 g/10 min when measured under ISO 1133-1:2022 at 230 °C with a 2.16 kg piston load, although the certificate of analysis for the specific production lot remains the controlling document. The material is intended for use as a sealant layer in coextruded cast film, blown film, and biaxially oriented polypropylene structures in which seal initiation temperature, hot-tack breadth, and optical clarity are critical conversion variables.
The three-monomer composition produces a distribution of macromolecular chain sequences that cannot be replicated by simple dry blending of a homopolymer with a random copolymer. This distinction matters on a production line because the thermal and rheological uniformity of the as-polymerized terpolymer determines the consistency of seal initiation temperature across a wound roll. In multilayer extrusion, a single-component terpolymer layer is preferred over a blend because the blend can separate under shear, producing local domains with higher melting point and erratic seal strength under ASTM F88/F88M-21.
Because the comonomer pair disrupts polypropylene helical ordering, the melting endotherm obtained by differential scanning calorimetry under ISO 11357-3 is broader and shifted to a lower temperature than that of a propylene homopolymer. This thermal shift is the primary source of the material’s lower seal initiation temperature, which is measured by ASTM F1921-18 or ASTM F88/F88M-21 and reported as the temperature at which a defined seal strength is achieved at a specified dwell time and pressure. The practical consequence is that downstream packaging lines can reduce sealing jaw set-points or increase line speed without a proportional loss in seal integrity.
The difference is not merely the presence of three monomer species; the distribution of ethylene and butene along the polypropylene chain determines crystallization kinetics, melting range, and the temperature dependence of seal strength. In a random copolymer, ethylene alone reduces the characteristic melting endotherm, but the chain still contains long crystallizable propylene sequences. In a terpolymer, the combined short-chain branching from 1-butene and the ethylene insertions reduces both the average sequence length and the crystal thickness distribution, producing a lower and broader melting endotherm under ISO 11357-3. The broader endotherm corresponds to a wider processing window between the onset of seal initiation and the onset of film distortion or shrink at the sealing jaw.
On cooling at 10 °C/min according to ISO 11357-3, the crystallization exotherm peak is shifted to a lower temperature than that of a homopolymer, which means the material remains amorphous for a longer time after leaving the die. This slower crystallization supports better melt-web contact on a chill roll and reduces quench-induced haze. The effect is measurable in cast film production as a reduction in surface haze under ASTM D1003-21 and as a more stable coefficient of friction on the skin layer.
For converters, the measurable variables are seal initiation temperature, hot-tack force, and optical haze. Seal initiation temperature is determined by heat-seal strength tests such as ASTM F1921-18 using a dwell time of 0.5 s and a pressure of 0.3 MPa; the reported value is the temperature at which seal strength reaches a threshold, commonly 0.5 N/15 mm. Hot-tack force is measured after a controlled seal is formed and immediately opened while the seal is still molten, using ASTM F1921-18 method B. Optical haze is measured by ASTM D1003-21 on a calibrated haze meter using a 50 μm cast film unless otherwise specified.
The direction of property change in a 4T05-class terpolymer is well documented. Compared with a propylene homopolymer of the same nominal melt flow rate, flexural modulus measured by ISO 178:2019 is lower, tensile yield stress measured by ISO 527-2:2012 is reduced, and haze measured by ASTM D1003-21 on a 50 μm cast film is generally lower because the smaller crystallite dimensions scatter less visible light. The trade-off is a reduction in upper-use temperature and load-bearing stiffness. The property shifts are acceptable in a lamination or sealant layer because the structural layers of a coextruded film supply mechanical stiffness while the sealant layer supplies the thermal sealing function.
Hot-tack force is the maximum force measured when a seal is opened before it solidifies. For a terpolymer, the hot-tack curve broadens toward lower temperatures because the lower crystallinity delays the solidification point. A typical hot-tack test on a 25.4 mm wide strip uses a seal pressure of 0.3 MPa, a dwell time of 0.5 s, and a peel speed of 200 mm/min; these parameters follow ASTM F1921-18. Reported hot-tack values are often quoted as the maximum force in newtons per 15 mm or newtons per 25 mm, requiring careful unit conversion when comparing suppliers.
| Property | Test method | Compared with homopolymer | Compared with random copolymer |
|---|---|---|---|
| Seal initiation temperature | ASTM F1921-18 | Lower by 25 K to 40 K | Lower by 8 K to 15 K |
| Flexural modulus | ISO 178:2019 | Reduced by 40% to 60% | Reduced by 10% to 25% |
| Haze on 50 μm cast film | ASTM D1003-21 | Lower, typically 0.5% to 2.0% absolute | Comparable or lower by 0.3% to 1.0% |
| Peak melting temperature | ISO 11357-3 | Lower by 20 K to 35 K | Lower by 5 K to 12 K |
| Tensile yield stress | ISO 527-2:2012 | Reduced by 35% to 55% | Reduced by 10% to 20% |
Published data for this specific configuration is limited; the table reports representative ranges from commercial terpolymer grades in the same melt-flow class and should not replace the supplier certificate of analysis for 4T05.
On a cast film line, 4T05 is processed as the skin layer of a coextruded structure. A typical configuration uses a 75 mm, 30:1 L/D single-screw extruder with a barrier screw and a Maddock mixing section, coupled to a feedblock and a slot die with a die gap of 0.8 mm to 1.2 mm. Melt temperature at the die is maintained between 220 °C and 240 °C, and the chill roll is held between 18 °C and 22 °C to limit post-crystallization haze development. Output stability depends on the extruder pressure profile; excessive back-pressure above 250 bar may indicate melt temperature override or inadequate screw design for this low-crystallinity grade.
On a blown film line, die gaps from 1.0 mm to 1.8 mm and blow-up ratios between 2.0:1 and 2.5:1 are used; the lower melt strength of the terpolymer relative to a high-melt-strength homopolymer requires closer control of the frost line height to prevent bubble sag. Pre-drying is not routinely required when the resin is supplied in moisture-protective packaging. If storage occurs at relative humidity above 60% or condensation is present on pellets, a desiccant dryer set to 70 °C to 80 °C for 2 h to 4 h with a dew point below −30 °C is applied before extrusion.
The grade’s lower melting point compared with homopolymer permits lower die temperatures, but the converter should not interpret this as an ability to use recycled homopolymer regrind without adjustment. Addition of more than 20% high-melt-flow homopolymer regrind to the sealant layer can raise the seal initiation temperature and narrow the hot-tack window because the homopolymer-rich domains crystallize first and dominate the failing interface. This incompatibility is not a chemical decomposition mechanism but a rheological and thermal shift that appears as erratic seal strength at low jaw temperatures. The material is not recommended for direct melt contact with high-polarity barrier polymers such as EVOH or polyamide without tie layers, because interfacial adhesion at PP/EVOH or PP/polyamide boundaries is insufficient; maleic anhydride grafted tie resins are required.
When a homopolymer sealant layer is replaced by 4T05 in a coextruded film, the seal initiation temperature drops sufficiently to allow sealing jaw temperature set-points to be reduced by 15 °C to 25 °C in typical vertical form-fill-seal equipment. The shift is measured by ASTM F88/F88M-21 on flat film and confirmed on the packaging machine by recording the minimum jaw temperature at which the 1.0 N/15 mm seal strength threshold is exceeded across 300 consecutive seals. This production-scale approach directly detects batch-to-batch variance because seal strength is sensitive to comonomer incorporation, additive migration, and film thickness variation.
The replacement also reduces flexural stiffness of the sealant skin, which can alter the bending stiffness of the entire laminate when the sealant layer exceeds 10% of total film thickness. In practice, sealant layers are commonly kept between 5% and 15% of total coextruded thickness, so the structural effect is limited. For applications that require a stiffer outer surface, the converter may compensate by increasing the homopolymer or core layer thickness rather than raising the 4T05 layer thickness beyond the seal-function requirement. Compared with olefin plastomers used as low-seal additives, 4T05 retains higher modulus and closer melt-flow compatibility with polypropylene layers, reducing viscosity mismatch at layer interfaces.
Regulatory compliance for 4T05 in food-contact film is evaluated under the olefin polymer provisions of FDA 21 CFR 177.1520 and EU Regulation 10/2011. Overall migration testing is performed according to EN 1186-1:2002 and specific migration methods depending on food simulant selection. The grade is also assessed under REACH 1907/2006 and RoHS Directive 2011/65/EU for heavy-metal restrictions. Suppliers provide a compliance statement for each production lot; downstream users must verify that the final laminate, ink, adhesive, and coating system meet end-use migration limits because the terpolymer layer alone is not the only source of migrating species.
| Regulation or standard | Scope | Test method or limit |
|---|---|---|
| FDA 21 CFR 177.1520 | Olefin polymers for food contact | Extraction testing as specified in the regulation; supplier certification required |
| EU 10/2011 | Plastic materials in food contact | Overall migration <10 mg/dm² per EN 1186-1:2002; specific migration for monomers as listed |
| RoHS Directive 2011/65/EU | Electrical and electronic equipment | Pb, Hg, Cd, Cr(VI), PBB, PBDE below 0.1% wt/wt; Cd below 0.01% wt/wt |
| REACH 1907/2006 | Registration and authorization | SVHC declaration below 0.1% wt/wt per article |