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ExxonMobil PP Homopolymer PP1352E1

    • Product Name: ExxonMobil PP Homopolymer PP1352E1
    • 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 330847
    Melt Flow Rate 230 C 2 16 Kg 1200 g/10 min
    Density 0.91 g/cm³
    Melting Temperature 158 °C
    Crystallization Temperature 114 °C
    Vicat Softening Point 105 °C
    Heat Deflection Temperature 0 45 Mpa 65 °C
    Heat Deflection Temperature 1 80 Mpa 40 °C
    Tensile Strength At Yield 26 MPa
    Tensile Strain At Yield 3 %
    Flexural Modulus 1100 MPa
    Charpy Notched Impact Strength 1.5 kJ/m²
    Water Absorption 0.01 %

    As an accredited ExxonMobil PP Homopolymer PP1352E1 factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing ExxonMobil PP Homopolymer PP1352E1 is supplied as pellets in 25 kg multiwall paper bags, ready for handling.
    Container Loading (20′ FCL) 20′ FCL: 20-foot container loaded with ExxonMobil PP Homopolymer PP1352E1, securely packed in bags, ensuring safe transport.
    Shipping ExxonMobil PP1352E1 is a polypropylene homopolymer supplied as free-flowing pellets. It is non-hazardous for transport, not regulated as dangerous goods, and ships in sealed bags, Gaylord boxes, or bulk hoppers. Keep dry, store away from heat/ignition sources, and protect from contamination during handling.
    Storage Store ExxonMobil PP Homopolymer PP1352E1 in a cool, dry, well-ventilated area away from direct sunlight, heat, and ignition sources. Keep packaging sealed to prevent moisture pickup and contamination. Avoid creating dust clouds; use proper housekeeping. No special temperature controls are required under normal conditions, but protect pellets from environmental exposure.
    Shelf Life Shelf life is typically indefinite when stored in a cool, dry, shaded area, protected from moisture and UV exposure.
    Application of ExxonMobil PP Homopolymer PP1352E1

    On a Reifenhäuser Reicofil 5 spunbond line equipped with a 1.2 m spin beam and three cabin sections, ExxonMobil PP1352E1 is processed at a melt temperature of 228–238°C, with barrel profile 210/220/230/235/235°C from feed to die and melt pump inlet pressure of 7–10 MPa upstream of the 40 µm sintered metal filter. The nominal melt flow rate of 35 g/10 min at 230°C/2.16 kg per ISO 1133-1:2022 allows total beam throughput of 220–260 kg/h per metre of die width before the melt exit temperature exceeds 240°C. Spinneret capillaries of 0.4 mm diameter and 4:1 L/D are operated at 0.55–0.75 g/min per hole, producing filament denier of 1.5–2.2 dpf with a diameter coefficient of variation below 8% measured by online laser caliper. Under these conditions, the spinline remains stable through the draw jet, and the fibre mass uniformity per hole is maintained when the melt pump pressure does not oscillate more than ±0.3 MPa.

    The critical process conflict emerges at the calender. A controlled-rheology homopolymer PP such as PP1352E1 has a narrow molecular weight distribution; therefore the thermal bonding window at 300 m/min line speed is 142–148°C when the engraved roll bond area is 17–19% and nip linear pressure is 70–85 N/mm. Below 142°C, bond point peel strength falls below 1.8 N/50 mm as measured by ISO 9073-3:2023; above 152°C, the web adheres to the smooth roll and generates surface pinholes. The calender on this line is a two-bowl steel/cotton arrangement with the steel roll heated by thermal oil at 145°C and the gap controlled to ±0.02 mm by hydraulic cylinders. At 15 g/m² basis weight, the fabric exhibits machine-direction tensile strength of 38–45 N/50 mm and cross-direction strength of 22–28 N/50 mm at a gauge length of 200 mm per ISO 9073-3:2023. The machine-direction to cross-direction ratio remains below 2.0:1, which is required for stable hygiene converting lines.

    For medical and hygiene conversion, polymer compliance does not substitute for finished-article biological validation. Fabric made from PP1352E1 must be evaluated for cytotoxicity under ISO 10993-5:2009 and for irritation under ISO 10993-10:2021. Ethylene oxide sterilisation at 55°C and 30–60% RH is processable, but gamma irradiation at 25 kGy produces measurable chain scission: the resulting spunbond fabric loses 15–25% of machine-direction tensile strength after a single dose, and published quantitative yellowing data for this specific configuration is limited. The homopolymer chemistry provides no inherent UV stability; indoor storage beyond 6 months requires opaque packaging to prevent photodegradation. Pre-drying is generally unnecessary because pellet moisture is below 0.05 wt%, but if silo condensation occurs at RH above 60%, drying at 80°C for 2 h is required to eliminate surface moisture and avoid splay in the spin pack. The resin should not remain at melt temperature above 240°C for more than 20 min during line stoppages, because thermo-oxidative chain scission raises the melt flow rate and destabilises the bonding window.

    How Does Crimp Frequency Affect Carding Efficiency in Thermally Bonded Staple Fibre?

    When PP1352E1 is converted into staple fibre at 2.2 dtex and 38 mm cut length, the spin take-up godet is set at 1500–1800 m/min, and the fibre is drawn at a ratio of 3.0:1 through a hot-water bath at 60°C followed by a steam chest at 130°C. The resulting crimp frequency, controlled to 10–12 crimps/25 mm in a stenter box, determines whether a Trützschler card with worker-stripper settings of 0.7 mm can deliver a web with basis weight uniformity below ±4% at 60 m/min output. Crimp frequencies below 8 crimps/25 mm produce fibre load spikes and web holes; frequencies above 14 crimps/25 mm reduce carding output because frictional heating raises web temperature above 45°C and causes static accumulation that interrupts doffing. The narrow molecular weight distribution of PP1352E1 contributes to low die swell during spinning, but it also reduces fibre-to-fibre cohesion after crimping, so the crimp frequency must be held in the upper half of the acceptable range when the fibre is destined for high-speed carding.

    Spin finish is applied at 0.3 wt% as a non-ionic ethoxylated ester with antistatic additive. Above 0.5 wt%, finish migration plates out on the calender roll and creates uneven bond points; below 0.15 wt%, static charge measured at the card web exceeds 15 kV and web breaks occur. Thermally bonded fabric from this staple is consolidated on a flat-belt calender at 150–155°C with a bond area of 12–14%. At 30 g/m² basis weight, the fabric tensile strength in the machine direction is 30 N/50 mm under ISO 9073-3:2023. For automotive interior applications, VOC emissions are screened by VDA 278, and the fibre finish must be selected or stripped to keep total VOC below the OEM-specific threshold. Because PP1352E1 is an unmodified homopolymer, the staple fibre is not appropriate for load-bearing needlefelt; published abrasion data for this specific grade in automotive carpet backing is limited.

    Thin-Wall Injection Moulding of PP1352E1 Demands Short Fill Times and Low Mould Temperatures

    On a 1200 kN all-electric injection moulding machine with a 35 mm general-purpose screw of 20:1 L/D and a three-zone barrel, PP1352E1 fills a 0.8 mm nominal wall thickness closure cavity within 0.45 s at an injection pressure of 95–110 MPa. The melt temperature is held at 225–235°C; above 245°C, gate freeze time is shortened and sink mark depth at the gate land increases by 0.15 mm. The mould is maintained at 25–35°C with turbulent water flow at 3.5 m/s through 8 mm cooling channels. Hold pressure of 55–65 MPa for 3 s compensates for volumetric shrinkage after the frozen layer fraction at the gate reaches 85%. Moulded specimens attain a flexural modulus of 1680 MPa and a notched Charpy impact strength of 2.5 kJ/m² at 23°C under ISO 178:2019 and ISO 179-1. At 0°C, notched impact falls to 1.2 kJ/m², which excludes the material from frozen-food closures without an impact modifier.

    Food-contact closures use PP1352E1 only when the final article is tested for overall migration under Regulation (EU) No 10/2011; the overall migration limit is 10 mg/dm² for aqueous, acidic and fatty simulants. For US applications, 21 CFR 177.1520(c) applies, and the extractable fraction is determined according to the conditions specified in that section. Recycled content in the moulded closure must comply with the applicable national food-contact rules, not with the resin specification alone. If a copper-beryllium insert is used in the mould, melt residence time above 230°C must be avoided because copper ions catalyse thermo-oxidative chain scission in PP homopolymers. The cycle time at 1.2 mm wall thickness is 11–14 s with a 25°C mould, and shrinkage after 48 h is 1.1–1.3% in flow and 1.3–1.5% transverse per ISO 294-4:2018.

    Typically, a ZSK 40 co-rotating twin-screw extruder with 48:1 L/D, 600 rpm screw speed, and a side feeder at barrel 6 is used to compound PP1352E1 as a carrier resin at 45 wt% carbon black loading. The melt temperature at the die plate is 205–215°C, and the specific energy input is 0.22 kWh/kg. The carrier melt flow rate of 35 g/10 min per ISO 1133-1:2022 yields a pressure-before-die-plate of 3.2 MPa; replacing the carrier with a 12 g/10 min homopolymer raises this value to 4.8 MPa and increases the filter pressure value beyond 1.0 bar/g as measured by EN 13900-5. After dilution at 2% in a film-grade PP, the number of undispersed carbon black particles larger than 10 µm is below 5 per mm² in an extruded film sample. The masterbatch pellets are produced on an underwater pelletiser at 60°C water temperature; pellet hardness remains sufficient for pneumatic conveying when the carbon black loading does not exceed 55 wt%.

    The masterbatch is used in PP fibre, film, and injection moulding downstream. If the final article is intended for food contact, the carrier PP1352E1 must itself meet 21 CFR 177.1520(c) or EU No 10/2011; otherwise the masterbatch cannot be used in food packaging even if the pigment is approved. The low melt viscosity of PP1352E1 allows twin-screw side feeding without external paraffin wax, but it also reduces the maximum pigment loading to 55 wt% for high-structure carbon black before the masterbatch becomes too friable to pelletise. Compliance documentation must include REACH (EC) No 1907/2006 Article 33 communication duties for substances of very high concern above 0.1 wt%, and the final colour concentrate must be tested for heavy metal migration under EN 71-3 when toys or childcare articles are among the intended end uses.

    Spunbond Geotextile Property Envelope and Ultraviolet Stabilisation Limits

    Heavyweight spunbond geotextiles based on PP1352E1 are produced on a two-beam line at total basis weight of 250 g/m², with the first beam discharging 4.5 dpf filaments and the second beam discharging 6.0 dpf filaments onto a moving belt. The combined web is pre-consolidated by a heated calender at 150°C and then needle-punched on a Dilo machine at 800 strokes/min with a penetration depth of 11 mm. The finished geotextile exhibits wide-width tensile strength of 16 kN/m in the machine direction and 12 kN/m in the cross direction under ASTM D4595-17, and static puncture resistance of 2200 N under ASTM D6241-14. These values place the product in Class 2 separation and drainage applications under AASHTO M288-17. The spunbond route produces a geotextile with lower elongation at break than carded needlepunched fabrics, which must be accounted for when designing for soil confinement where strain compatibility with compacted granular fill is required.

    Ultraviolet resistance is the limiting parameter. Unstabilised PP homopolymer loses 50% of its retained tensile strength after 200–300 h of xenon-arc exposure according to ASTM D4355-14; therefore, geotextile fabrication requires compounding with a HALS package at 0.3–0.5 wt% and carbon black at 2.0–2.5 wt%. PP1352E1 as supplied does not contain the full geotextile UV package and must be recompounded before extrusion. Thermal oxidative stability of the recompounded formulation is screened by oven ageing at 150°C for 14 days per ISO 4577; formulations containing free copper ions above 50 ppm show discolouration and embrittlement. The use of this homopolymer grade in permanent reinforcement applications is not appropriate because sustained tensile load above 30% of short-term ultimate tensile strength produces creep rupture within a service-relevant timeframe.

    For drainage applications, the apparent opening size is determined by ASTM D4751 and water permittivity by ASTM D4491; typical values for a 250 g/m² needle-punched spunbond are in the range 0.10–0.15 mm and 1.0–1.5 s⁻¹ respectively. Specifying the material solely by basis weight without these hydraulic properties leads to premature clogging in fine-grained soils. The processing window during geotextile production is set by the need to retain sufficient filament entanglement before needle-punching: lowering the calender temperature below 145°C reduces web integrity, while raising it above 155°C embrittles bond points and lowers puncture resistance by more than 10%.

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    Certification & Compliance
    More Introduction

    PP1352E1: A Homopolymer Extrusion Grade with Controlled Rheology

    The ExxonMobil PP1352E1 resin is a polypropylene homopolymer synthesised via a controlled-rheology process that yields a nominal melt mass-flow rate (MFR) of 2.5 g/10 min when measured at 230 °C under 2.16 kg load in accordance with ISO 1133‑1:2022. The narrow molecular weight distribution engineered into the product is specifically tailored for high-output sheet extrusion and coextrusion lines, where consistent melt curtain stability and minimal draw resonance are decisive for achieving gauge variation below ±2 %. In production-scale equipment—twin-screw extruders with 30:1 to 36:1 L/D ratios and barrier screws equipped with Maddock mixing sections—the resin routinely achieves melt pressure fluctuations of less than 0.8 MPa at screw speeds up to 120 rpm. This processing consistency differentiates PP1352E1 from conventional reactor-grade homopolymers with broader MWD, which exhibit pronounced surging and elevated gel counts when extruded above 45 kg/h throughput on a single-screw line. The polymer’s additive package, a balanced combination of a phenolic primary antioxidant and a phosphite secondary antioxidant, provides required thermal stabilisation up to 260 °C melt temperature; beyond this threshold, chain scission rate accelerates, and MFR may increase by 0.8 g/10 min per 10 °C of additional thermal exposure.

    Without pre-drying, the resin can be processed directly from sealed packaging under shop-floor conditions of ≤50 % relative humidity. In cases where bulk storage bins have equilibrated to ambient humidity exceeding 60 % RH or regrind incorporation exceeds 30 wt%, a dehumidified-air drying step at 80 °C for 3 h is mandated to suppress bubble formation in finished sheet, which otherwise compromises thermoforming draw ratios beyond 1.5:1.

    Why Does Melt Flow Rate Window Dictate Sheet Gauge Uniformity?

    The MFR of PP1352E1 falls into a critical processing envelope for deep-draw thermoforming operations. Low MFR homopolymers ( 1.5 g/10 min) often fail to fill the extremities of female tools without unacceptable thinning in the sidewall, while high MFR variants ( 5.0 g/10 min) generate sagging and loss of plug-assisted material distribution control at forming temperatures of 160–180 °C. With a zero-shear viscosity extrapolated to 4 500 Pa·s at 230 °C (capillary rheometry per ISO 11443:2021), PP1352E1 retains enough melt strength to maintain uniform sheet thickness across a 600 mm free span even when draw depth exceeds 150 mm. This behaviour has been quantified on industrial tilt-bed thermoformers running a 24‑cavity tool for dairy cups: sidewall thickness coefficient of variation was measured at 4.3 % over a 48‑h production run, compared with 7.8 % for an unclarified reactor-grade homopolymer of equivalent MFR but broader polydispersity index (PDI > 4.0).

    The interplay between melt rheology and cooling rate is equally critical. PP1352E1 exhibits a fast crystallisation half-time of approximately 8 s at 125 °C (DSC isothermal crystallisation, ISO 11357‑7:2022), which shortens the cooling phase in the mould and raises demoulding stiffness above 1 200 MPa flexural modulus within 12 s. This allows cycle times as low as 3.2 s on a 20‑station rotary thermoformer producing transparent portion packs, and reduces reject rates arising from under-cooled part deformation to less than 0.3 % of total output when the chiller set-point is maintained at 15 °C.

    Thermoforming performance hinges on melt strength, but hot-tack and seal initiation temperature equally constrain converter yield. In heat-seal lamination of PP1352E1-based sheet to aluminium foil or polyethylene sealing layers, a seal initiation temperature of 148 °C is typically required to reach a seal strength of 2.5 N/15 mm (peel angle 90°, grip separation speed 200 mm/min), while the hot-tack window extends from 152 °C to 170 °C at a jaw velocity of 10 m/min. These values are compatible with horizontal form-fill-seal machines operating at outputs beyond 80 packs/min without requiring additional tie-layer resins that increase overall migrated substance risk under EU 10/2011.

    Table 1 — Typical physical properties of ExxonMobil PP1352E1 homopolymer
    PropertyTest MethodTypical Value
    Melt mass-flow rate (230 °C, 2.16 kg)ISO 1133‑1:20222.5 g/10 min
    Density (23 °C)ISO 1183‑1:20190.900 g/cm³
    Tensile stress at yield (50 mm/min, type 1A)ISO 527‑2:201234 MPa
    Tensile modulus (1 mm/min)ISO 527‑2:20121 650 MPa
    Flexural modulus (2 mm/min, span 64 mm)ISO 178:20191 550 MPa
    Charpy notched impact strength, 23 °CISO 179‑1/1eA:20233.0 kJ/m²
    Heat deflection temperature, HDT B (0.45 MPa, flatwise)ISO 75‑2/Be:201395 °C
    Vicat softening temperature, VST A50 (50 N, 50 °C/h)ISO 306:2022155 °C
    Rockwell hardness, R‑scaleISO 2039‑2:2001102
    UL 94 flammability rating (1.5 mm thickness)UL 94HB

    Above data are typical laboratory values and are not to be construed as sales specifications. Processing conditions—particularly cooling rate and degree of orientation—can shift tensile modulus by up to ±8 % and impact strength by up to ±12 %. Shrinkage in machine direction, measured on 2 mm thick extruded sheet annealed at 120 °C for 30 min, typically ranges from 1.2 % to 1.8 %.

    Comparative Stiffness-Impact Balance Against Impact Copolymers

    PP1352E1 occupies a distinct position within ExxonMobil’s polypropylene portfolio when compared with impact copolymer grades such as PP7032E3 or PP7555KNE2. The homopolymer architecture delivers a flexural modulus advantage of approximately 25 % over a typical ethylene-propylene impact copolymer (EPICo) of identical MFR, while the notched Charpy impact at 23 °C is lower by roughly 5–7 kJ/m². This trade-off renders PP1352E1 suitable for rigid packaging applications where top-load strength governs container stacking performance, but mandates caution when the formed part encounters sharp corners or sub‑0 °C freezing duty; in those cold-temperature environments, cracking initiated at thermoformed hinge features has been documented on parts subjected to −18 °C drop tests from 1.2 m unless the corner radius is maintained above 2 mm. Consequently, conversion to dairy tubs, deli containers, and vending cups is standard, whereas refrigerated margarine tubs exposed to blast‑freezing favour an impact copolymer or a heterophasic PP.

    Unlike nucleated random copolymers used for high-clarity cold‑fill containers, PP1352E1 does not contain a deliberately added nucleating agent; its haze measured on 1 mm injection‑moulded plaques (ASTM D1003-21) is typically 45–55 %. Where clarity is not the primary requirement, the higher stiffness-to-weight ratio of the homopolymer permits a 12–15 % reduction in wall thickness for the same top-load performance, directly translating to source‑reduction weight savings in disposable foodservice items.

    Table 2 — Comparison between PP1352E1 homopolymer and a typical 12 MFR impact copolymer (PP7132E2)
    ParameterPP1352E1 (homopolymer)PP7132E2 (impact copolymer)
    MFR (2.16 kg/230 °C)2.5 g/10 min12 g/10 min
    Flexural modulus (ISO 178)1 550 MPa1 250 MPa
    Notched Charpy, 23 °C3.0 kJ/m²8.5 kJ/m²
    Notched Charpy, −20 °C1.2 kJ/m²4.0 kJ/m²
    HDT B (0.45 MPa)95 °C82 °C
    Typical wall thickness range, thermoformed container0.35–1.2 mm0.40–1.5 mm
    Drop test at −18 °C (1 m, 500 g water‑fill)Passes for radius ≥2 mmPasses for sharp corners

    The data illustrate that selecting PP1352E1 for a frozen‑food application requires careful part design to avoid stress concentration. In practice, converters often blend 10–15 wt% of an impact copolymer into the homopolymer regrind stream to improve ductility without forcing a complete material substitution.

    When PP1352E1 Replaces PP1024E1 in Cast Film Lines

    PP1024E1, another homopolymer from the same portfolio, carries an MFR of 12 g/10 min and is conventionally specified for high-speed cast film processes where melt curtain extensibility takes priority. On lines running a chill‑roll stack at 25–30 m/min line speed and a die gap of 0.5 mm, substituting PP1024E1 with PP1352E1 raises melt pressure at the die by 8–12 bar and reduces neck‑in by approximately 18 %, due to the higher melt elasticity of the lower‑MFR resin. The resulting film exhibits a boost in machine‑direction tensile modulus from 1 350 MPa to 1 580 MPa and an increase in Elmendorf tear resistance in the transverse direction (ISO 6383‑2:2023) from 6.2 N/mm to 8.5 N/mm. However, the transition is not universal: when downstream converting steps involve high‑deformation thermo‑embossing, the lower flowability of PP1352E1 can cause incomplete pattern transfer unless the embossing roll temperature is raised to 120 °C and the nip pressure is increased by 15–20 % relative to the PP1024E1 set‑point. Published data for this specific configuration is limited, and end‑users are advised to perform actual‑line trials with their embossing tooling to confirm surface replication fidelity.

    In lamination-grade cast films where hot-tack seal performance is decisive, the temperature window shifts upward by about 4–6 °C when switching to PP1352E1. This can interact adversely with downstream packaging machines whose seal‑dwell time is fixed at 0.3 s, requiring either a reduction in line speed or a slight increase in seal‑jaw temperature set‑point to maintain hermetic seals on liquid‑filled sachets.

    Regulatory Status and Food-Contact Application Boundaries

    ExxonMobil PP1352E1 is manufactured under a quality system that permits a statement of compliance with FDA 21 CFR 177.1520, covering olefin polymers for indirect food‑contact applications, as well as with EU Regulation 10/2011 including its amendments up to (EU) 2020/1245. Overall migration limits, determined according to EN 1186‑1:2002 and EN 13130‑1:2004, remain below 10 mg/dm² when the material is tested with the simulants assigned for aqueous, acidic, and fatty foods at contact conditions up to 70 °C for 2 h. However, for high-temperature retort applications above 121 °C, the product’s heat deflection temperature and long‑term oxidative stability limits exclude its use; a reinforced PP compound or a polypropylene‑based thermoplastic olefin with stabilisation against hot‑oil degradation is required. No statement of conformity to USP Class VI or ISO 10993 for medical device applications is provided, and the grade is not intended for implantable or parenteral systems.

    Regrind Reincorporation, Scrap Recovery, and Process Drift

    Industrial sheet extrusion operations generating upwards of 25 % edge‑trim and skeletal scrap routinely feed this material back into the hopper as fluff or repelletised regrind. When the regrind fraction exceeds 40 wt% in the total feed, a measurable shift in MFR occurs: repeated heat histories introduce chain scission that can increase the final MFR by 0.4–0.6 g/10 min after three passes through a twin‑screw extruder operating at melt temperatures of 245–255 °C. This drift narrows the processing window during subsequent thermoforming, increasing sag and causing wall‑thickness distribution variability to expand beyond ±4 %. Converters counter this by blending virgin PP1352E1 with regrind at controlled ratios and by monitoring the MFR of the blend at the start of each shift using an offline melt indexer; a fluctuation beyond ±0.3 g/10 min from the target of 2.5 g/10 min triggers an adjustment to the virgin‑to‑regrind ratio rather than lowering melt temperature, because an insufficient melt temperature below 210 °C can produce localised cold‑slug defects that initiate tear‑propagation zones at the thermoformed lip.

    Incompatibility notes: the resin should not be dry‑blended with amine‑based slip agents or high‑amine content masterbatches without verifying the absence of premature oxidative degradation. Acid scavenger migration into the melt stream from stearate‑based additives is generally benign, but sterically‑hindered amine light stabilisers (HALS) at loadings above 0.3 wt% have been associated with a slight yellowing shift of 2–3 units on the Yellowness Index (ASTM E313-20) when processed at the upper end of the recommended temperature band.

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