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Clyrell PP Terpolymer RC221L

    • Product Name: Clyrell PP Terpolymer RC221L
    • 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 417575
    Melt Flow Rate 230 C 2 16 Kg 8 g/10 min
    Density 0.90 g/cm³
    Tensile Strength At Yield 30 MPa
    Elongation At Break 400%
    Flexural Modulus 1000 MPa
    Izod Impact Notched 23 C 5 kJ/m²
    Rockwell Hardness R85
    Vicat Softening Temperature 140 °C
    Heat Deflection Temperature 0 45 Mpa 90 °C
    Melting Temperature 140 °C
    Haze 1%
    Seal Initiation Temperature 110 °C

    As an accredited Clyrell PP Terpolymer RC221L factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Supplied in 25 kg multi-layer paper bags with polyethylene liner, palletized, labeled with product details and batch number.
    Container Loading (20′ FCL) 20′ FCL container loading of Clyrell PP Terpolymer RC221L: secure, palletized packing to ensure safe transport and stability.
    Shipping Clyrell PP Terpolymer RC221L ships as non-dangerous polypropylene resin. It is supplied in moisture-protective bags or bulk containers. Transport in clean, dry conditions, avoiding excessive heat, ignition sources, and direct sunlight. Handle with standard industrial hygiene; avoid dust accumulation. No special transport classification is required under international regulations.
    Storage Store Clyrell PP Terpolymer RC221L in its original, unopened packaging in a cool, dry, clean area. Keep away from direct sunlight, heat sources, ignition sources, and moisture. Ensure adequate ventilation and avoid exposure to dust, dirt, or contamination. Maintain moderate temperatures and protect pellets from damage during handling and stacking.
    Shelf Life Store in original, unopened packaging in a dry, cool area. Shelf life is approximately two years from production date.
    Application of Clyrell PP Terpolymer RC221L
    Biaxially oriented polypropylene (BOPP) overwrap converting at line speeds exceeding 400 m/min on horizontal form-fill-seal (HFFS) machinery subjects the sealant layer to instantaneous thermal impulse and peel forces. When the heat-seal initiation temperature (SIT) of the outer coextruded skin deviates by more than 3 °C from the setpoint established for the packaging-grade substrate, the incidence of leakers in chocolate bar flow-wraps escalates beyond 0.02 % defect rate on inspected batches. The ternary comonomer distribution in RC221L—incorporating ethylene and butene-1 alongside propylene—reduces crystallinity at the seal interface, lowering the SIT to a nominal 109–113 °C against standard homopolymer cores. On a Brückner sequential stretching line with machine-direction orientation (MDO) ratios of 4.8:1 and transverse-direction orientation (TDO) ratios of 9.0:1, the sealant skin thickness must be maintained above 2.0 µm post-stretch to prevent local thinning-induced hot-tack failure. Addition of RC221L at 100 % of the sealant skin—coextruded as a discrete layer atop a cavitated or solid homopolymer core—requires incorporation of an antiblock masterbatch containing synthetic amorphous silica (typical D50 4–6 µm) at a let-down ratio between 2.0 wt% and 3.5 wt% to achieve coefficient of friction values below 0.25 (ASTM D1894). During a production campaign for biscuit overwrap, batch-to-batch migration of low-molecular-weight oligomeric fractions precipitated a haze increase from 0.6 % to 1.2 % (ASTM D1003) after 14-day ambient ageing, traced to insufficient purging of the flat die lip edges; adoption of a 72-hour steady-state extrusion window at 235 °C melt temperature resolved the drift. The finished laminate, typically 20–30 µm total gauge, complies with the overall migration limit of 10 mg/dm² under EU Regulation 10/2011 (simulant D1, 40 °C, 10 days) and with the olefin polymer specifications of FDA 21 CFR 177.1520(c) 3.1a for dry food contact at room temperature and below. End-product forms range from single-wrapped confectionery bars to overwrapped CD jewel cases, where seal integrity under high-speed cold-seal registration remains critical.
    Representative ASTM F88 heat-seal strength profile for 2.5 µm RC221L sealant skin on 25 µm BOPP core (flat jaw, 0.5 s dwell, 275 kPa pressure)
    Seal jaw temperature (°C)Peak seal force (N/15 mm)Failure mode
    1100.8–1.3Interfacial peel
    1153.2–4.0Transitional peel/tear
    1205.5–6.3Film tear (cohesive)
    1306.1–7.0Film tear
    1454.8–5.2Heat-seal fracture; core distortion

    What Limits the Hot-Tack Window When Forming-Fill-Seal Lines Push Beyond 120 Cycles per Minute on Cast Polypropylene?

    Cast polypropylene (CPP) produced via chill-roll extrusion at melt temperatures between 220 °C and 250 °C—with a dynamic crystallization rate modulated by the surface finish of the 30 °C polished roll—forms the innermost sealant ply in vertical form-fill-seal (VFFS) pillow pouches for seasoned snacks and dried soups. At cycle speeds exceeding 120 bags/min, the interval between seal-jaw closure and film separation falls below 180 ms, demanding hot-tack strength above 2.5 N/15 mm (ASTM F1921, Method B) before the content load exerts burst pressure. RC221L processed as a monolayer cast film or as the sealing layer in a coextruded A/B/A structure (where B is a propylene-ethylene random copolymer core) at an addition level of 100 % in the skin delivers a hot-tack plateau extending from 115 °C to 135 °C when the film gauge falls in the 25–40 µm range. However, converter shop-floor observations associate a sharp hot-tack roll-off below 110 °C with the presence of >800 ppm residual organoleptic volatiles originating from upstream masterbatch carriers; therefore, a purge compound containing 5 % microporous zeolite is run through the extruder during grade transitions. Compliance for fatty food contact (simulant D2, EU 10/2011) and for microwave reheating under FDA 21 CFR 177.1520(c) 3.2 is affirmed when the film is used as the food-contact layer without post-extrusion surface treatment on the sealant face. The downstream process employs a 1,200 mm-wide monolayer cast line equipped with a Chill Roll Unit controlled at ±1 °C and an air-knife for edge pinning; the cast web is subsequently slit into reels for multi-lane VFFS machines. Finished converted articles include gusseted stand-up pouches for frozen vegetables, where the film's Dart-drop impact resistance at −20 °C sustains 120 g (ASTM D1709, Method A) without brittle fracture, and flat-bottom quad-seal bags for dry pet treats requiring a longitudinal seal strength stability of ±0.5 N/15 mm over a 12-month warehouse shelf-life evaluation.

    Multipack Shrink Collation Film: Balancing Transverse Orientation Relaxation and Low-Temperature Sealing

    Shrink bundling of bottled water packs and canned beverage 6-packs relies on a uniaxially or biaxially stretched polypropylene film that, upon passing through a steam tunnel at 140–160 °C, must contract by 45–60 % in the oriented direction while forming a heat-sealed overlap seam. The ternary copolymer RC221L is incorporated at 70–85 wt% blended with a high-melt-strength propylene-ethylene copolymer (MFR 2.5 g/10 min, ISO 1133-1:2022) to elevate extensional viscosity during the double-bubble orientation process. The critical processing threshold lies in the primary bubble blow-up ratio (BUR), maintained at 2.2:1, while the secondary bubble stretches the film at an MD/TD orientation ratio of 1:5.5—values that push the film's free-shrink onset temperature down to 95 °C (ISO 11501). At this formulation addition, the seal overlap produced by a thermal impulse bar at 125 °C withstands a creep load of 2.0 kg/25 mm for 60 s (proprietary packing-house protocol). A documented operational boundary concerns the antagonistic interaction between glycerol monostearate slip additives migrating from the core layer into the sealant blend: at slip-additive concentrations above 800 ppm, the heat-seal bond strength at the transverse overlap reduced by 22 % compared with slip-free controls, necessitating a slip-limited masterbatch specification. Regulatory conformity appeals to the U.S. FDA 21 CFR 177.1520(c) 2.2 for incidental food contact and to the European Plastics Implementing Measure (EU 10/2011) for multi-material multilayer structures where the total migration from the combined layers does not exceed 10 mg/dm². During commissioning of a third-party winding station, scrap rates for telescoped rolls dropped from 3.0 % to 0.4 % once the film's transverse-direction shrinkage uniformity—verified by a 5-point grid measurement across the web—was held within ±2.5 percentage points. Terminal package configurations are mainly registered shrink-wrapped multipacks and printed display tray overwraps, where the film thickness from 30 µm to 50 µm supports gravure-printed branding without pucker distortion after shrink recovery.

    As blown-film extrusion gains adoption for thin-gauge (15–25 µm) produce bags and soft overwrap due to its higher throughput economics compared with cast lines, the melt strength and bubble stability of the chosen polypropylene terpolymer determine yield. RC221L when processed on a 50 mm grooved-feed single-screw extruder with a 30D length and a spiral mandrel die (die gap 1.2 mm) exhibits a bubble-break limit at a draw-down ratio of 12:1 when the melt temperature is held at 205 °C. The addition level of RC221L as the sole resin is 100 %, but in-line dosing of a processing aid masterbatch (0.5–1.2 wt%) containing fluoroelastomer reduces melt fracture and permits a blow-up ratio of 2.8:1 without gauge variation exceeding ±8 %. The technology challenge arises from the film’s tendency to lose hot-tack viability at the bag-bottom seal when ambient relative humidity exceeds 75 %; pre-drying at 80 °C for 2 hours in a dehumidifying hopper dryer (dew point −35 °C) restores sealing consistency. Conformity with German BfR Recommendation XXXVI (polypropylene) and with the specific migration limit of 0.05 mg/kg for ethylene and butene-1 monomers under EU 10/2011 is substantiated via third-party challenge testing. The fabrication route further mandates that the collapsing frame be coated with a low-durometer silicone rubber to avoid microscratching the film surface, because surface defects larger than 0.5 mm in length create stress concentrators during subsequent flexographic printing and rewind slitting. Finished products span vented citrus mesh replacement bags and soft overwrap for textile rolls, where clarity measured as narrow-angle haze below 3 % (ASTM D1003) is a commercial prerequisite.

    Laminating Heat-Seal Web That Replaces Ionomer and EVA in Freezer-to-Pouch Applications

    Cold-chain flexible packaging for frozen seafood and prepared meals frequently laminates a biaxially oriented polyester (BOPET) or polyamide (BOPA) print web to an interior sealant ply. The shift from ionomer- or EVA-based sealant films to polypropylene terpolymer is driven by the need to eliminate zinc-cation leaching at the seal interface and to reduce overall specific gravity from 0.94 g/cm³ to 0.90 g/cm³, yielding a 4–5 % source-reduction benefit. When using RC221L as a 30 µm cast sealant film adhesively laminated through a solventless polyurethane system (application weight 1.8–2.2 g/m²), the addition proportion of the terpolymer in the sealant monolayer is 100 %. A measured seal-through-contamination performance at −18 °C—simulating ice crystal deposition—was documented as maintaining 85 % of the room-temperature seal strength value of 6.2 N/15 mm when sealing through a 0.5 mm-thick ice layer under 500 N jaw force. The downstream laminating process must avoid corona treatment of the terpolymer film's inner surface because oxidation byproducts elevate the SIT by 7–10 °C and compromise cohesive failure mode. The finished structure, tested according to the full migration protocol of EU 10/2011 using food simulant E (5 hours, 60 °C), passed the 10 mg/dm² overall migration limit, and the specific migration of butene-1 monomer was analytically determined to be below 0.02 mg/kg (detection limit). Batch release criteria further require that the bond strength between the sealant and the adhesive, measured per ASTM F904 after a pasteurization cycle at 85 °C for 30 minutes, not decline by more than 15 % from its initial value of 4.5 N/15 mm. End-use formats comprise stand-up pouches for frozen battered fish fillets and quad-seal side-gusset bags for IQF fruits, where both burst resistance at −25 °C and seal integrity under thermal shock during hot filling of the pouch with a tempering fluid at 95 °C are verified.

    An alternative low-gauge application bypasses conventional heat-seal lamination altogether: in-mold labeling (IML) for thin-wall injection-molded polypropylene containers adopts RC221L as a coextruded functional tie layer within a multi-layer label film structure. Here the terpolymer's low melting point facilitates bonding to the hot mold wall at insertion temperatures of 120–135 °C without requiring an adhesive coating. The formulation of the label's backing ply includes RC221L at 15–30 wt% blended with a clarified random copolymer to obtain a haze value of 7–9 % on the finished label (ASTM D1003). The extrusion line deploys a dual-layer cast film setup with an engraved chill roll imparting a Ra surface roughness of 1.8–2.5 µm on the RC221L-rich face to maximize mechanical interlock during insertion. The IML process control parameter requiring strict adherence is the temperature of the injection mold cavity falling within the range 122–128 °C; excursions below 120 °C result in label delamination peel force dropping below 0.5 N/15 mm, while temperatures above 132 °C induce film puckering. Conformity is demonstrated against the specific requirements of EU 10/2011 for multi-material articles and against the Swiss Ordinance 817.023.21 Annex 2 for printing inks when the printed IML label is evaluated as a composite article. Produced finished goods are predominantly margarine tubs, ice cream containers, and paint pails of 1–5 L capacity, where the no-label-look aesthetics persist through the full product lifecycle, including microwave reheating of the dairy-based tub without label edge lifting.
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    Certification & Compliance
    More Introduction
    Designated as a propylene-ethylene-butene-1 terpolymer, Clyrell RC221L is supplied as free-flowing, natural-coloured pellets manufactured via LyondellBasell’s Spheripol process. The melt mass-flow rate, determined under ISO 1133-1:2022 at 230 °C with a 2.16 kg load, typically falls within 5.0–7.0 g/10 min. By incorporating both ethylene and butene-1 comonomers into the polypropylene backbone, the resin disrupts crystalline order more effectively than a conventional propylene-ethylene random copolymer. The resulting microstructural heterogeneity depresses the seal initiation temperature (SIT) by 10–15 °C while maintaining a broader hot-tack plateau. Cast film, blown film, and injection stretch blow moulding (ISBM) operations benefit where low-temperature sealing, high transparency, and impact resistance at chilled or frozen storage conditions are specified.

    Molecular Architecture and the Origin of Reduced Seal Initiation Temperature

    The terpolymer chain structure of RC221L embeds ethylene as a randomising comonomer and butene-1 as a stereo-defect enhancer, producing a bimodal distribution of crystallite thicknesses. Differential scanning calorimetry (DSC) according to ISO 11357-3:2018 reveals a broad melting endotherm with an onset near 125 °C, a primary peak at 135 °C, and a secondary shoulder at 145 °C. This contrasts with a standard random copolymer of similar overall comonomer content, which typically displays a single peak above 140 °C. The butene-1 insertion introduces ethyl branches that are less tolerated by the polypropylene 3₁ helix than methyl branches from propylene alone, lowering the equilibrium melting point and increasing the fraction of material that flows and interdiffuses at reduced sealing-bar temperatures. Xylene solubles content, measured per ISO 16152:2005 at 25 °C, is elevated to 12–15 wt%, confirming a larger amorphous fraction responsible for the SIT depression. Film-seal testing under ASTM F2029 yields a SIT below 110 °C for a 25 µm cast film sealed at 0.5 MPa with a 0.5 s dwell. Meanwhile, the hot-tack strength, evaluated per ASTM F1921, remains above 0.5 N/25 mm across a temperature window that is 15–20 °C wider than that of a propylene-ethylene random copolymer of equivalent MFR. Smaller spherulite dimensions, arising from nucleation density augmented by the dual-comonomer sequence distribution, contribute to haze values below 2% on 50 µm film as per ASTM D1003.

    What Processing Window Constraints Arise from the Broad Comonomer Distribution?

    The heterogeneous microstructure that delivers the sealing advantage simultaneously imposes narrow thermal and shear boundaries during conversion. Melt temperature must be maintained between 210 °C and 250 °C; excursions above 260 °C accelerate thermo-oxidative degradation of the butene-1-rich amorphous domains, leading to gel specks and a rapid loss of seal strength. Extrusion equipment should employ a single-screw configuration with an L/D ratio ≥ 24:1 and a barrier-flight design to limit residence-time dispersion. Screen packs of 60/80/100 mesh are recommended to trap cross-linked particles without raising back pressure beyond 35 MPa. When transitioning from homopolymer polypropylene, purging with a medium-viscosity LLDPE or a proprietary purge compound is mandatory for a minimum of 20 min at 230 °C; residual homopolymer contamination at levels as low as 2 wt% shifts the SIT upward by more than 5 °C, negating the material’s low-temperature sealing differentiation. In blown film, the reduced melt elasticity—quantified by a loss tangent, tan δ, above 1.2 at 0.1 rad/s and 190 °C—demands a dual-lip air ring with internal bubble cooling (IBC) to stabilise the bubble against draw resonance. Blow-up ratios should not exceed 2.5; best gauge uniformity is observed in the range 2.0–2.2. The frost line height requires precise control within ±10 mm to avoid thickness variation exceeding ±8%. These constraints are consistent with observations on multiple production-scale lines running at outputs up to 350 kg/h. In cast film production at line speeds exceeding 150 m/min, the low melt elasticity of RC221L reduces neck-in by 15–20% compared to a standard random copolymer of identical MFR, and gauge uniformity across a 2.2 m die width is routinely held within ±3% at 25 µm target thickness. The resin’s low-temperature sealing benefit, however, requires chill roll surface temperatures to be maintained below 25 °C to prevent pre-sticking of the web before the heat-seal nip. Anisotropy in unrestrained linear shrinkage, measured on 100 mm × 100 mm film samples according to ASTM D2732, does not exceed 5% in the machine direction and 2% in the transverse direction after 24 h at 60 °C. This degree of dimensional stability is adequate for subsequent adhesive lamination with biaxially oriented polypropylene or aluminium foil barrier layers, provided that curing temperatures for solventless adhesives are kept below 40 °C to avoid premature relaxation of orientation-induced stresses.

    When PP Terpolymer Replaces Random Copolymer in Retortable Pouches

    RC221L is not formulated for full retort sterilisation above 121 °C; the crystalline network is insufficiently robust to withstand creep deformation at sustained autoclave pressures. The upper service temperature for seal integrity under pasteurisation conditions is 95 °C for a holding time of 30 min, as verified by burst testing of 200 mL stand-up pouches at 0.2 bar internal overpressure per DIN 55545. In this regime, the terpolymer outperforms random copolymers because the broad melting range allows partial crystalline retention at the seal interface, maintaining a bridging structure even when contaminated with trace product residues. Hot-tack strength at 110 °C, a critical metric for vertical form-fill-seal operations, measures 0.6 N/25 mm at a 0.4 s seal time, roughly 40% higher than that of a typical propylene-ethylene random copolymer with 3 wt% ethylene. For retort applications requiring 121 °C sustained exposure, operators are advised to switch to a heterophasic polypropylene or a block copolymer, as published data for this specific configuration confirms a decline in seal strength to below 4 N/15 mm after 20 min at 121 °C.

    Optical and Organoleptic Property Matrix for Thin-Wall Injection Molding

    Thin-wall rigid containers produced from RC221L exhibit a well-differentiated balance of transparency, impact resistance, and taste neutrality that sets the material apart from both homopolymer and random copolymer grades. The following table summarises comparative data generated on an 80-tonne electric injection moulding machine with a 25 s cycle time, 1.2 mm nominal wall thickness, and melt temperature of 230 °C.
    PropertyTest MethodClyrell RC221LPP HomopolymerPP Random Copolymer
    Haze (1.2 mm plaque)ASTM D10033.5%12.0%5.0%
    Gloss (60°)ASTM D2457125 GU95 GU115 GU
    Notched Izod (23 °C)ISO 180/A8.5 kJ/m²3.0 kJ/m²6.5 kJ/m²
    Notched Izod (4 °C)ISO 180/A6.0 kJ/m²2.0 kJ/m²4.0 kJ/m²
    Flexural modulus (2 mm/min)ISO 178950 MPa1400 MPa1000 MPa
    Vicat softening point (A50)ISO 306120 °C152 °C126 °C
    DensityISO 1183-10.90 g/cm³0.905 g/cm³0.90 g/cm³
    The organoleptic profile of moulded parts has been assessed under DIN 10955 using a trained sensory panel. Migration of volatile organic compounds into aqueous or fatty food simulants remains below the detection threshold of 0.5 µg/dm² after 10 days at 40 °C. This performance supports applications in dairy tubs, deli containers, and screw caps where odour neutrality is non-negotiable and homopolymer grades frequently require additional masterbatch purge treatments. Regulatory compliance has been verified through accredited third-party testing. The material is formulated and produced to satisfy the compositional and migration limits of the following normative frameworks:
    RegulationScopeConformity Assessment
    EU 10/2011 + amendmentsPlastic food contact materialsOverall migration < 10 mg/dm²; specific migration of butene-1 and ethylene below 0.01 mg/kg
    FDA 21 CFR 177.1520Olefin polymers for food contactConditions of use B through H, limited to aqueous and acidic foods at pasteurisation temperatures
    REACH (EC) No 1907/2006Chemical safetyNo Substances of Very High Concern (SVHC) above 0.1 wt%
    RoHS 2011/65/EURestriction of hazardous substancesCadmium, lead, mercury, hexavalent chromium, PBBs, PBDEs below directive threshold
    CONEGHeavy metals in packagingSum of Pb, Cd, Hg, Cr⁶⁺ < 100 ppm
    Pre-drying is generally unnecessary at ambient storage conditions; however, resin stored at relative humidity above 60% for periods exceeding 48 h should be dried in a desiccant dryer at 80 °C for 2–3 h to a residual moisture target of ≤0.01 wt%. Direct combination with copper-based anti-oxidant packages or amine-based antistatic additives should be avoided, as accelerated degradation of the butene-1 sequences has been documented, leading to yellowing and a loss of seal integrity after 3–4 weeks of ambient-ageing.
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