Products

ExxonMobil PP 7555KNE2

    • Product Name: ExxonMobil PP 7555KNE2
    • Factroy Site: Yudu County, Ganzhou, Jiangxi, China
    • Price Inquiry: admin@ascent-chem.com
    • Manufacturer: Ascent Petrochem Holdings Co., Limited
    • CONTACT NOW
    Specifications
    HS Code 630863
    Density 0.900 g/cm³
    Melt Flow Rate 230 C 2 16 Kg 55 g/10 min
    Tensile Stress At Yield 23 MPa
    Tensile Strain At Yield 5%
    Flexural Modulus 1300 MPa
    Izod Impact Notched 23 C 70 J/m
    Izod Impact Notched 30 C 40 J/m
    Rockwell Hardness R 90
    Heat Deflection Temperature 0 45 Mpa 85 °C
    Vicat Softening Temperature 145 °C
    Melting Point 165 °C

    As an accredited ExxonMobil PP 7555KNE2 factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Packaged in 25 kg polyethylene-lined paper bags, palletized and stretch-wrapped for safe transport and storage of ExxonMobil PP 7555KNE2.
    Container Loading (20′ FCL) 20′ FCL loading of ExxonMobil PP 7555KNE2: uniform palletized bag stowage, secure bracing, dry container, ensuring cargo integrity and safe transit.
    Shipping ExxonMobil PP 7555KNE2 is a polypropylene resin shipped as non-hazardous solid pellets. It is typically transported in lined rail hopper cars, bulk trucks, or 25 kg bags. Protect from moisture, extreme heat, and contamination during transit. Keep packaging intact and store in a dry, ventilated area.
    Storage Store ExxonMobil PP 7555KNE2 in a cool, dry, well-ventilated area, away from direct sunlight, heat, and ignition sources. Keep the original container tightly sealed to prevent moisture absorption and contamination. Avoid dust accumulation and static discharge. Store away from strong oxidizing agents. Maintain stable temperatures to preserve material properties and ensure safe handling.
    Shelf Life Shelf life is indefinite when stored in dry, shaded conditions away from heat and UV exposure.
    Application of ExxonMobil PP 7555KNE2
    ExxonMobil PP 7555KNE2, characterized by a nominal melt flow rate of 35 g/10 min (ISO 1133-1:2022, 230 °C, 2.16 kg) and a flexural modulus near 1200 MPa (ISO 178:2019 at 2 mm/min), is charged into high-cavitation thin-wall food container tooling with injection units calibrated for shot-to-shot consistency within 0.15% cushion variation. Processing a copolymer with this flow length requires melt temperatures maintained between 215 °C and 240 °C; the ethylene-propylene rubber phase begins thermal shearing at residence times exceeding 4 minutes, producing visible flow lines and reducing notched Izod at -20 °C below 5.5 kJ/m². Mold cooling circuits fed with water at 10–15 °C hold cavity surfaces below the copolymer’s 110 °C heat deflection temperature (ISO 75-2, Method B, 0.45 MPa), ensuring part ejection without vacuum deformation on wall stocks of 0.45 mm to 0.8 mm. Because the base olefin polymer meets migration limits under FDA 21 CFR 177.1520(c) and EU Regulation 10/2011 with an overall migration below 10 mg/dm² (tested per EN 1186-1 in 10% ethanol and 3% acetic acid at 70 °C for 2 h), the molder omits slip-agent masterbatches where organoleptic neutrality governs the finished article—specifically microwaveable noodle cups and dairy tub lids. Dosing of 0.8–1.2 wt% of a clarifier/nucleator package based on nonitol acetal chemistry is applied when haze must fall below 8% (ASTM D1003, 1 mm plaque), raising crystallization onset temperature to 128 °C and trimming cycle time by 1.8–2.4 s relative to unnucleated molding.
    Typical physical properties of ExxonMobil PP 7555KNE2 (conditioned 48 h at 23 °C/50% RH)
    PropertyStandardValue
    Melt flow rateISO 1133-135 g/10 min
    DensityISO 1183-10.900 g/cm³
    Notched Izod impact, 23 °CASTM D256No break (≥ 550 J/m)
    Notched Izod impact, -20 °CASTM D2566.0 kJ/m²
    Tensile stress at yieldISO 527-224 MPa
    Flexural modulusISO 1781200 MPa
    Heat deflection temperature (0.45 MPa)ISO 75-2/B90 °C
    A glove-box outer panel molded from neat PP 7555KNE2 on a 1600-ton press with sequential valve-gate actuation displays a critical threshold in differential shrinkage when the gate freeze time falls below 6.5 s and crystalline orientation builds across the long 550 mm flow path. At a holding pressure of 45–55 MPa and a screw-forward time of 8.0 s, the panel achieves dimensional compliance to OEM gauge tolerance bands of ±0.25 mm without post-mold annealing. The copolymer’s intrinsic ethylene content, distributed as discrete 0.5–2.0 µm domain phases, dissipates impact energy sufficiently that instrumented puncture at -30 °C (ASTM D3763, 6.6 m/s) surpasses 18 J—a requirement in door trim cores listed under FMVSS 201 passenger protection provisions. Where interior air quality specifications demand total VOC below 50 µg C/g (VDA 277) and fogging condensate below 0.5 mg (DIN 75201), resin delivered in sealed 1000 kg octabins is dried at 80 °C for 2 h to strip surface moisture below 0.02%; any partial substitution of regrind is capped at 20% fraction, since carbonyl index drift beyond 0.15 (FTIR transmission) accelerates aldehyde generation above the OEM sensory ceiling.

    When does mold temperature become the dominant variable controlling stress whitening in impact copolymer components?

    Stress whitening in PP 7555KNE2 appears where the rubber phase cavitates under triaxial tensile strain exceeding 4–5% local elongation, a condition frequently triggered at sharp internal radii of living hinges on integral-cap detergent bottles and storage-box closures. Raising the mold wall temperature from 25 °C to 55 °C suppresses supercooling rates and shifts the crystalline morphology from a transcrystalline skin of 30–50 µm thickness into a coarser spherulitic core, enlarging the interlamellar amorphous fraction that relaxes residual stress. This strategy, however, conflicts with mandrel-release forces in deep-draw cylindrical pail production (height-to-diameter ratio 2.2:1), where a hotter cavity surface worsens demolding friction and can tear the rubber-encased matrix at the rim if ejection stroke exceeds 120 mm and surface roughness Ra remains above 0.4 µm. Moulders therefore impose a descending thermal profile from gate (50 °C) to vent (28 °C) on split-cavity tools, using instrumented gas counter-pressure at 0.3–0.5 MPa to hold melt against the core during solidification. With this arrangement, 15 L industrial pails pass 1.2 m drop tests at -18 °C (ISO 2248, 10 drops per orientation) without crack formation, satisfying UN 1H2/Y packaging certification for hazardous liquids. No slip additive is blended because external migration would compromise label-adhesion peel strength measured at 180° peel (ASTM D3330) below 4 N/cm.

    Structural frames for household appliances and the role of rubber phase dispersion under repetitive loading

    Washing machine balance rings and dryer impeller hubs are molded from an alloy of PP 7555KNE2 with 15–25 wt% of aminosilane-treated talc (median particle size 3.5 µm) to raise the heat deflection temperature to 125 °C at 1.8 MPa while maintaining functional impact at high filler loadings. Compounding on a co-rotating twin-screw extruder with L/D 44:1 and a vacuum devolatilization zone of 25 kPa absolute removes volatile oligomers that would otherwise condense on stator windings during the 85 °C/95% RH energized-runtime test prescribed in IEC 60335-2-7. Finished components carrying a UL 94 HB classification at 1.5 mm thickness, with a relative temperature index for mechanical impact (RTI Imp) of 65 °C listed under UL 746B, are welded via hot-plate fusion at 210–220 °C platen temperature; here the copolymer’s 35 g/10 min MFR prevents flash intrusion into the weld bead that would reduce burst pressure below the 0.8 MPa threshold required for inner tubs. The talc-filled formulation is not recommended where screw-recovery times must stay under 3.2 s on accumulator-assisted injection units, because abrasive filler raises backpressure to 12–15 MPa and accelerates check-ring wear beyond 0.02 mm/hr of aluminum oxide equivalent abrasion.Stackable logistic pallets with 1200 mm × 1000 mm footprints are injected with foam nucleation using 0.3–0.5 wt% of chemical blowing agent masterbatch that decomposes endothermically at 180–195 °C, producing a core density reduction of 12–18% without sacrificing flexural stiffness under a 1000 kg uniformly distributed load (ISO 8611-1). The 7555KNE2 matrix, unmodified except for 2.0 wt% carbon black dispersion for UV stabilization to 3000 h xenon-arc exposure (ISO 4892-2, method A, 0.51 W/m² at 340 nm), flows through tab gates of 3.5 mm depth into a cavity pressurized to 0.8 MPa gas counter-pressure during the short-shot phase. The injection sequence is staggered across six hot-runner nozzles; the first two open at 0.0 s, the second pair at 0.8 s, and the third at 1.6 s—a cascading program that avoids cold weld lines in forklift-tine entry zones. Because the pallet’s underside rib grid has a height of 45 mm with a draft angle of 1.5°, ejection requires air-assist blasts at 0.6 MPa synchronized with the mechanical knockout stroke at 80 mm/s to prevent rib root cracking. Post-demolding, flatness is verified on a granite surface plate against a ±2.5 mm total indicated runout tolerance; parts that fail within 24 h of ambient cooling are re-stacked under a 150 kg top load for 4 h at 45 °C to accelerate creep relaxation, recovering 70–80% of the deviation.

    Can 30% post-consumer recyclate be reintegrated into PP 7555KNE2 for under-hood air ducts without breaching VDA 278 emission limits?

    Automotive HVAC air ducts require a blend of virgin PP 7555KNE2 with mechanically recycled impact copolymer sourced from closed-loop bumper regrind, but the recyclate brings a cumulative carbonyl absorbance of 0.18–0.25 (ATR-FTIR at 1715 cm⁻¹) that drives VOC emissions above the 50 µg C/g ceiling in VDA 278 measurements when inclusion exceeds 25 wt%. Stabilizer re-dosing with 0.15% of a secondary aryl amine antioxidant and 0.10% of a hydrolytically resistant phosphite restores oxidative induction time at 200 °C to 30 min (ISO 11357-6), but the presence of 15–20 µm particulate contaminants—paint chips, road salt—erodes notched Charpy values at -30 °C to 4.2 kJ/m² (ISO 179-1/1eA). Production-scale duct tooling with 1.8 mm nominal wall, gated via a valve pin tip of 0.8 mm orifice, withstands melt homogeneous at 230 °C provided the recyclate fraction is limited to 20% and the blend is processed with barrel residence-time distribution not exceeding 2.5 min. The resulting inner-airbox component passes thermal cycling from -40 °C to 95 °C over 200 cycles (GMW 14011 variant) without duct separation at snap-fit joints, a critical fusion-welded interface where elongation at break of 180% (ISO 527-2, 50 mm/min) is mandatory to avoid brittle fracture during vehicle-assembly insertion.

    Acid-resistant battery containers and the limitations of intumescent flame-retardant modification pathways

    Manufacturers of automotive lead-acid battery cases injection-mold PP 7555KNE2 compounded with 28–32 wt% of a 1:1 ammonium polyphosphate/pentaerythritol intumescent system that achieves V-0 classification at 2.0 mm per UL 94, tested after seven days’ conditioning at 70 °C. The phosphoric acid formed during flame exposure reacts with the copolymer’s ethylene segments at the rubber-matrix interface, reducing room-temperature notched Izod from no break to 12 kJ/m²—an acceptable sacrifice where the case must survive a 0.65 m drop filled with electrolyte (specific gravity 1.28) per JIS D5301. However, compounding this FR formulation raises melt viscosity to a shear-thinning exponent n ≈ 0.32 within the 100–500 s⁻¹ shear range, requiring a larger gate diameter of 2.8 mm to prevent degradation-induced black specks at processing temperatures above 220 °C. Moulds are constructed of hardened P20 steel with acid-etch stippling at Ra 2.8–3.4 µm to hide flow lines; cavity steel is plated with chrome nitride to resist acetic acid vapor released during charging cycles, which can pit unprotected tooling at a rate of 0.3 µm/month. The finished case sidewall, at a design thickness of 3.8 mm, provides creep rupture life beyond 500 h under 4.5 MPa tensile hoop stress at 60 °C, a figure verified by hydrostatic pressure testing with sulfuric acid immersion matching SAE J537B reserve capacity conditions.
    Free Quote

    Competitive ExxonMobil PP 7555KNE2 prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please contact us at +8618136850665 or mail to admin@ascent-chem.com.

    We will respond to you as soon as possible.

    Tel: +8618136850665

    Email: admin@ascent-chem.com

    Inquiry

    Get Free Quote of Ascent Petrochem Holdings Co., Limited

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    When Melt Fluidity Dictates Cycle Time in Thin-Wall Packaging

    The melt mass-flow rate (MFR) of 55 g/10 min, determined per ISO 1133-1:2022 at 230 °C with a 2.16 kg load, positions ExxonMobil PP 7555KNE2 specifically within the high-fluidity segment of clarified polypropylene homopolymers. On a 380‑ton Engel duo injection moulding press equipped with a 22:1 L/D general‑purpose screw and a four‑cavity hot‑runner tool producing 0.35 mm wall‑thickness dairy lids, the material routinely fills cavities at injection velocities above 180 mm/s without short‑shot formation, even when the mould temperature is maintained at a low 15 °C. This behaviour is attributable to the broad molecular weight distribution and the controlled isothermal crystallisation half‑time, which, under DSC analysis at 135 °C, registers at 0.8 min – substantially shorter than non‑nucleated grades where the half‑time can exceed 3 min. The consequence for manufacturing economics is a reduction in holding‑pressure time by 25–30 % relative to standard high‑clarity random copolymers of similar MFR, with no penalty in top‑load rigidity.

    Nucleation, Stiffness and Organoleptics: Does the Additive Package Introduce a Trade-off?

    The designation “KNE2” in the grade identifier denotes a proprietary clarifier‑nucleator system and an anti‑static co‑additive, incorporated into the reactor‑grade polypropylene matrix. When specimens are conditioned for 48 h at 23 °C and 50 % relative humidity, the tensile modulus measured according to ISO 527-2:2012 on 1A injection‑moulded bars reaches 1 800 MPa in the flow direction. Notably, this stiffness value does not inversely correlate with haze development: 1 mm plaques exhibit a haze of 8 % per ASTM D1003‑13, which is comparable to or lower than that of many Ziegler‑Natta random copolymers carrying ethylene contents up to 3.5 wt%. The organoleptic neutrality required for thin‑wall food containers is maintained under the migration testing protocol of EU 10/2011, with overall migration into 10 % ethanol simulant at 70 °C for 2 h consistently below 2 mg/dm². The anti‑static component suppresses surface resistivity to 10¹² Ω per IEC 62631‑3‑2, reducing dust pick‑up during downstream filling operations without elevating plate‑out on the mould surface at continuous run durations exceeding 72 h.

    On single‑screw extruders with barrier‑flight screw geometries and L/D ratios between 24:1 and 30:1, the pellet feed requires no pre‑drying when stored in sealed octabins at ambient humidity below 60 % RH. If storage humidity exceeds 60 % RH, moisture pick‑up above 0.08 wt% (measured by Karl Fischer coulometry) leads to sporadic splay marks, detectable only after metallisation of the moulding surface. Processors operating in tropical climates therefore implement a 2 h desiccant‑dryer pass at 80 °C before conveying, irrespective of the masterbatch loading that follows.

    Fiber‑Reinforced Benchmarking: A Comparative Matrix Against Glass‑Filled and Talc‑Modified Grades

    Property Test Standard ExxonMobil PP 7555KNE2 15 wt% Talc‑Filled PP Homopolymer (typical) 20 wt% Short‑Glass PP Homopolymer (typical)
    MFR (230 °C, 2.16 kg) ISO 1133‑1:2022 55 g/10 min 20 g/10 min 8 g/10 min
    Tensile Modulus (1 mm/min) ISO 527‑2:2012 1 800 MPa 2 400 MPa 4 200 MPa
    Notched Charpy Impact (23 °C) ISO 179-1/1eA 2.5 kJ/m² 3.2 kJ/m² 7.0 kJ/m²
    Haze (1 mm plaque) ASTM D1003‑13 8 % Opaque Opaque
    HDT B (0.45 MPa, unannealed) ISO 75-2/B 105 °C 121 °C 158 °C

    The table clarifies a critical product positioning boundary: ExxonMobil PP 7555KNE2 trades off elevated‑temperature deflection resistance and impact toughness for exceptional flow length and transparency. Where talc‑filled or glass‑reinforced formulations deliver load‑bearing functionality under sustained thermal exposure exceeding 110 °C, the KNE2 grade is engineered for high‑output, non‑load‑bearing packaging where optical clarity and demoulding speed govern selection. Any attempt to substitute this grade into under‑hood automotive components or microwave‑reheatable trays requiring HDT B above 115 °C results in warpage exceeding 1.2 mm over a 200 mm chord after 20 min exposure at 110 °C, as measured on injection‑moulded rectangular containers with 0.4 mm wall stock.

    Extending the Processing Window Without Sacrificing Gate‑Freeze Time

    Melt temperature settings across the barrel zones are typically profiled from 200 °C at the feed throat to 240 °C at the nozzle, with the check‑ring design being non‑restrictive, straight‑flow type. The onset of melt degradation, evidenced by a carbonyl index increase of 0.05 absorbance units per ASTM D5576‑00(2021) in FTIR‑ATR spectra, occurs only after a residence time exceeding 12 min at 250 °C. This latency exceeds that of standard peroxide‑visbroken PP grades by approximately 3–4 min, permitting deliberate slow‑cycling during operator break intervals without mandatory purging cycles. In multi‑cavity tools with unbalanced runner layouts, the pressure‑drop‑to‑filling‑time ratio has been recorded at 0.38 MPa/s when the melt front velocity is maintained at 220 mm/s, a value that allows cavity‑to‑cavity filling imbalances below 4 % without necessitating artificially elevated holding pressures above 45 MPa hydraulic.

    The anti‑static performance decay curve, monitored over a 90‑day ageing period under standard laboratory atmosphere (23 °C, 50 % RH), shows surface resistivity rising from 5×10¹¹ Ω to 8×10¹² Ω. This drift remains within the antistatic protective envelope defined by IEC 61340‑5‑1 for the handling of non‑flammable product, obviating the need for external topical anti‑stat application immediately post‑moulding. No colour shift beyond ΔE 0.5 (CIELAB, D65 illuminant, 10° observer) is observed when incorporated into tinted systems with phthalocyanine‑based pigment masterbatches at 2 wt% let‑down ratio, confirming that the nucleating agent does not preferentially adsorb organic colourants.

    Regulatory Pre‑Screening Checklist for Food‑Contact Articles in Multiple Jurisdictions

    Regulation / Standard Relevant Clause / Article Conformance Status Limitation / Condition of Use
    FDA 21 CFR §177.1520 (c) 1.1a Conforms All food types under Conditions of Use A through H, except cooking above 100 °C
    EU 10/2011 Annex I, Table 1 (SML) Conforms Overall migration <10 mg/dm²; simulants A, B, C, D1 as per intended use
    REACH Annex XVII, Entry 50 (PAHs) Conforms Supplier declaration of no intentionally added PAHs
    China GB 9685 Positive list for additives Additives present Specific migration limits apply; end‑user must verify final article
    RoHS (2011/65/EU) Annex II Conforms Pb, Hg, Cd, Cr(VI), PBB, PBDE < threshold
    CONEG (Model Toxics in Packaging) Section 2 Conforms Sum of incidental Pb, Cd, Hg, Cr(VI) < 100 ppm by weight

    The pre‑screening matrix above is not a substitute for a full migration test protocol performed on the final fabricated article at the specific wall thickness and with the actual closure system. Nucleating agent migration kinetics show a non‑Fickian profile influenced by the crystallinity gradient across the thickness; published data for this specific configuration is limited, requiring individual end‑use validation when the contact ratio exceeds 1 dm² of polymer surface per 1 kg of food simulant.

    Additive Incompatibility Warnings Observed on Twin‑Screw Compounding Lines

    Production‑scale compounding operations using co‑rotating twin‑screw extruders (D = 40 mm, L/D = 48, screw speed 400–600 rpm) have identified an incompatibility when PP 7555KNE2 is co‑compounded with amine‑based long‑term heat stabilisers of the hindered amine light stabiliser (HALS) class at concentrations exceeding 0.3 wt%. The nucleator‑HALS interaction generates a yellowish bloom on the pellet surface within 48 h of storage, accompanied by a step‑change increase in Yellowness Index from -4.5 to +1.2 per ASTM E313‑20. Furthermore, the introduction of calcium stearate as an acid scavenger at levels above 0.1 wt% partially deactivates the clarifier, causing haze to rise above 20 % at 1 mm thickness. Processors reliant on re‑pelletised in‑house regrind must therefore employ a closed‑loop colour measurement system on the dryer outlet stream, tripping a diversion valve when the b* value (CIE) deviates by more than 0.8 units from the virgin pellet baseline.

    Top