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Exelene PP Homopolymer H2000

    • Product Name: Exelene PP Homopolymer H2000
    • 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 760183
    Melt Flow Rate 230 C 2 16 Kg 8 g/10 min
    Density 0.90 g/cm³
    Tensile Strength At Yield 34 MPa
    Elongation At Yield 10%
    Flexural Modulus 1500 MPa
    Izod Impact Strength Notched 23 C 3 kJ/m²
    Heat Deflection Temperature 0 45 Mpa 100 °C
    Vicat Softening Point 155 °C
    Rockwell Hardness R 110
    Melting Point 165 °C
    Water Absorption 24 H 0.01%
    Thermal Conductivity 0.22 W/m·K

    As an accredited Exelene PP Homopolymer H2000 factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Exelene PP Homopolymer H2000 is supplied as solid pellets in 25 kg multi-layer paper bags, palletized and shrink-wrapped.
    Container Loading (20′ FCL) 20′ FCL: 25 kg bags on palletized, shrink-wrapped loads, securely stowed and protected for safe transport.
    Shipping Exelene PP Homopolymer H2000 ships as non-hazardous polypropylene pellets in sealed multiwall paper or foil-lined bags and bulk supersacks. Protect from moisture, direct heat, and UV light. Store in a dry, ventilated area between 15–30°C. Avoid dust accumulation and ground transfer equipment to prevent static discharge.
    Storage Store Exelene PP Homopolymer H2000 in a cool, dry, well-ventilated area away from direct sunlight, heat, open flames, and strong oxidizers. Keep containers tightly sealed to prevent moisture contamination and dust accumulation. Avoid static electricity buildup; use proper grounding if transferring. Maintain a clean environment and protect packaging from mechanical damage to preserve product quality.
    Shelf Life Store in a cool, dry place away from heat and sunlight. Shelf life is typically indefinite if packaging remains sealed and intact.
    Application of Exelene PP Homopolymer H2000

    Exelene PP Homopolymer H2000, characterized by a nominal melt flow rate of 2.0 g/10 min (ISO 1133-1:2022, 230°C/2.16 kg) and a homopolymer backbone absent of ethylene comonomer, exhibits a crystallinity range of 55–62% as determined by differential scanning calorimetry at a heating rate of 10 K/min. This narrow molecular weight distribution resin is supplied with a standard antioxidant package based on a synergistic blend of hindered phenolic and phosphite stabilizers, enabling processing stability up to 250°C for a residence time not exceeding 8 minutes. The absence of nucleating agents in the base formulation necessitates consideration of cooling rate effects on final part stiffness and shrinkage anisotropy. The following scenarios delineate the technical boundary conditions under which this grade integrates into manufacturing lines where lot-to-lot consistency in torque during compounding or injection metering is the primary acceptance criterion.

    When Melt Flow Ratio Hits 2.16 at 230°C — The Injection Molding Window for PP H2000 in IML Food Containers

    In-mold labeling (IML) production of thin-wall round dairy tubs with a target wall thickness of 0.45 mm and a flow length-to-thickness ratio exceeding 220:1 places stringent demands on the zero-shear viscosity of the molten phase. The homopolymer H2000, processed on a fully electric injection molding machine with a clamp force capacity of 3,500 kN and a 3-zone screw of L/D 22:1, is typically introduced at a melt temperature of 245°C ± 3°C and an injection velocity profile ramping from 45 mm/s to 110 mm/s over the filling stroke. This temperature setpoint is deliberately maintained above the crystalline melting peak of 162°C to prevent premature skin solidification in the 0.8 mm diameter hot runner nozzle tips. The 2.0 MFR resin is frequently dry-blended with 1.5–2.0 wt% of an endothermic chemical foaming agent masterbatch based on sodium bicarbonate–citric acid chemistry to achieve a core density reduction of 8–12%, which compensates for the inherent shrinkage of the homopolymer phase without compromising top-load rigidity. The formulation compliance with Regulation (EU) No 10/2011 on plastic materials intended to come into contact with food is addressed through the use of the specific migration limit (SML) database; the antioxidant blend in H2000 is pre-certified for overall migration below 10 mg/dm² under test conditions of 40°C for 10 days using food simulant D1 (EN 1186-1:2002). The thermodynamic constraint arises during mold cooling: a cavity surface temperature kept at 12–15°C via turbulent-flow water circuits ensures that the label substrate (60 μm cast polypropylene film) does not delaminate, yet cooling below 10°C induces transcrystallinity at the label–melt interface, increasing the risk of brittle failure along the label edge when the filled container undergoes a drop test of 1.0 m at 4°C. On the production floor, the process is monitored using in-cavity pressure transducers with a sampling rate of 500 Hz, and the switch-over point from velocity to pressure control is triggered at a cavity pressure of 380 bar to minimize flash formation while ensuring replication of the label texture. Finished articles are margarine tubs and yogurt cups of 250–500 mL capacity, rated for microwave reheating at 800 W for 2 minutes without deformation when containing an emulsion of fat content not exceeding 5%.

    Air Intake Manifolds Underhood: Sustaining Continuous Service at 110°C with 30% Glass Fiber Reinforcement

    The substitution of metal in naturally aspirated intake manifolds requires a compound that survives hot soak temperatures up to 120°C in the engine bay while resisting creep under constant negative pressure of −50 kPa at 90°C. Exelene H2000 serves as the matrix phase in a formulation containing 30 wt% chopped E-glass fibers of 11 μm diameter and 4.5 mm targeting fiber length retention above 0.8 mm post-compounding on a twin-screw corotating extruder with a processing section of L/D 40:1 and a vacuum venting zone at −0.8 bar. Twin-screw kneading blocks with a staggering angle of 60° are positioned to minimize fiber attrition; residual fiber length distribution is verified by incineration at 600°C and optical microscopy per ISO 11358-1:2014. The compounded pellets are injection molded in a mold equipped with gas-assist technology using nitrogen at a gas pressure of 15 MPa applied after a short shot that fills 92% of the cavity volume; this produces hollow channel walls with a wall thickness tolerance of ±0.2 mm. The thermal oxidative stability of this glass-filled homopolymer composition is evaluated by long-term heat aging at 140°C in an air circulating oven according to ISO 4577:2019; a retained tensile strength of at least 70% after 1,000 h is considered the minimum industrial acceptance criterion for the intake manifold module. Additionally, the material’s creep modulus at 100°C and 10 MPa applied stress must remain above 1,400 MPa after 500 h (ISO 899-1:2017) to prevent gasket sealing failure. Potential processing incompatibilities include the formation of acetic acid from the coupling agent (aminopropyltriethoxysilane) when moisture is present in the glass rovings above 0.15% by weight; this catalyzes backbone chain scission at elevated barrel temperatures. Thus, pre-drying of glass fiber at 80°C for 4 hours is mandatory, and the hopper of the injection unit is blanketed with dry air at a dew point of −30°C. The terminal component is an assembled acoustic-tuned manifold for a four-cylinder gasoline engine, meeting flammability standard FMVSS 302 with a burn rate below 80 mm/min on specimens conditioned for 48 h at 23°C/50% RH.

    When the extrusion direction is transverse to the conveyor belt, the melt is distributed through a coat-hanger die with a lip gap adjusted to 0.6 mm and a die body temperature profiled from 260°C at the edges to 240°C at the center to counteract the viscosity-velocity profile mismatch. The extrudate then enters a series of polished chill rolls with a diameter of 500 mm, where the first roll is maintained at 85°C and the second at 60°C to induce a quiescent cooling gradient that suppresses formation of beta-phase spherulites—detrimental to long-term dimensional stability. This sheet, specifically produced from Exelene H2000 without any impact modifier, is subsequently scored and thermoformed on a continuous plug-assisted machine using a preheat oven zone at 175°C surface temperature, forming cycle time of 2.8 s, and a plug material of syntactic foam to minimize heat dissipation. The forming accuracy directly affects the stacking feature of the resulting load-bearing pallet liners and returnable dunnage trays used in automotive tier-1 supplier logistics. The material’s compliance with ISO 8611-1:2021 for reusable plastic flat pallets is validated through a corner drop test at 0.5 m load with a 500 kg contained mass, where the absence of brittle fracture in the hinge area is the pass/fail determinant. A processing caution emerges from the narrow window: at sheet extrusion rates exceeding 450 kg/h, surging in the gear pump arises due to the high melt elasticity of the narrow MWD homopolymer, mitigated by adding 0.1 wt% of a fluoropolymer-based processing aid that reduces the critical shear rate for melt fracture onset from 120 s⁻¹ to below 200 s⁻¹ at 240°C. The resultant products are collapsible sleeves and conductive-grid containers meeting electrostatic discharge requirements per IEC 61340-5-1, with surface resistivity modulated to 10⁴–10⁶ Ω/sq via a loading of 3 wt% conductive carbon black masterbatch, a combination that leverages the homopolymer’s purity since ionic stabilizers from copolymers would otherwise poison conductivity.

    What Prevents Melt Fracture in High-Speed Spunbond Line with Exelene H2000?

    Fine denier spunbond nonwoven fabrics for medical gowns and surgical drapes require fibers with a filament diameter of 15–20 μm produced at take-up speeds of 3,000–3,500 m/min. The rheological suitability of H2000 in this process hinges on its narrow molecular weight distribution (polydispersity index ~2.8–3.2), which delays the onset of melt fracture to higher shear rates compared to broad-MWD commodity homopolymers. On a Reicofil-type single-beam line, pellets are gravity-fed into a single-screw extruder with a length of 30D and a grooved feed section operating at a barrel temperature profile rising from 180°C to 240°C, and then delivered to a spin beam through a metering pump maintaining a pressure of 8–12 MPa. The spinneret is equipped with capillaries of 0.3–0.4 mm diameter and a L/D ratio of 4:1; a custom additive package composed of 0.15 wt% erucamide (slip agent of CI 4:13 amide) and 0.15 wt% calcium stearate (CaSt) is pre-compounded to stabilize spinline oscillation and reduce hydroperoxide formation during drawing. Within the quench zone, air at 12°C and a velocity of 0.8 m/s impinges on filaments, rapidly cooling them below the crystallization onset temperature of 128°C; the draw ratio is controlled between 120:1 and 150:1 to achieve an orientation that elevates the amorphous phase glass transition to an effective service point of −5°C. The resulting fabric is thermally bonded using an engraved calender with a point fraction of 18.5% at a roll temperature of 165°C and a nip pressure of 70 N/mm. Barrier performance against synthetic blood under hydrostatic pressure (ISO 16604:2004) is delivered by a post-treatment with a fluorocarbon-based repellent finish applied at 0.8 g/m² add-on, not by matrix modification. Optical brightening agents are omitted entirely to comply with the EN 13795:2019 requirement for the absence of dermal-toxicity residues. A documented constraint is that the resin must be pre-dried to a moisture content below 50 ppm in a hot-air desiccant dryer before extrusion; failure to do so results in an increase in the filament breakage rate from a standard 0.2% to above 3.5%, as measured by the fiber interruption counter on the drawing unit. The final lot is rolled into surgical isolation gown fabric of 35 g/m² basis weight, which also passes the ASTM F1671-13 viral penetration test under Phi-X174 bacteriophage challenge.

    Battery cell spacers and busbar holders in electric vehicle prismatic module assembly are subjected to a continuous operating temperature of 65°C with intermittent spikes to 85°C during fast-charging events. Exelene H2000 compounded with 15 wt% short glass fiber and 3 wt% halogen-free intumescent flame retardant (based on ammonium polyphosphate phase I/II blend with a phosphorus content of 21%) is injection molded into flat insulating plates with a thickness of 2.0 mm and a rib design that provides creepage distances conforming to IEC 60664-1:2020, pollution degree 2. The melt temperature during molding is set to a narrow window of 250–255°C; excursions above 255°C trigger premature intumescence and generate free phosphoric acid species that corrode chrome-plated mold surfaces. The flame retardant formulation achieves a UL 94 V-0 classification at 2.0 mm thickness after conditioning at 70°C/50% RH for 168 h, and the Comparative Tracking Index (CTI) is measured as 525 V (IEC 60112:2020), which exceeds the 400 V threshold generally accepted for insulation material in lithium-ion packs. In the assembly station, the injection-molded spacer is placed between cell pouches using an automated handling system that relies on a coefficient of thermal expansion mismatch not exceeding 12 × 10⁻⁵ K⁻¹, measured in the flow direction by thermomechanical analysis (ISO 11359-2:2021), to avoid gap formation after temperature cycling. A field experience note: early batches that skipped the removal of low-molecular-weight oligomers from the homopolymer (via a two-stage vacuum devolatilization step during compounding) exhibited measurable deposition of condensable volatile compounds on the cell terminal welds, increasing contact resistance by 8% after 500 thermal cycles from −30°C to +80°C. Acceptable limits for total volatile organic content (VOC) in the resin are therefore specified as <0.5 µg/g as benzene equivalent using headspace gas chromatography with flame ionization detection per VDA 277:2017. The finished component is a cell retention frame with integrated snap-fit latch, serving in a nominal 400 V battery system compliant with UN/ECE R100.

    Chemical Resistance Validation for 5-Layer Coextruded Blow Molded Containers

    A 5-layer coextrusion blow molding process produces containers of 500 mL to 5 L capacity intended for filling with anionic surfactant solutions (pH 8.5–9.5) and low-concentration hydrogen peroxide (3.5% aqueous). The layer structure comprises a virgin Exelene H2000 skin, an adhesive tie layer of maleic anhydride-grafted polypropylene, a central ethylene-vinyl alcohol (EVOH) barrier layer, a second tie layer, and an inner layer of post-industrial recycled H2000 regrind at a ratio of up to 30 wt%. The accumulator head of a shuttle-type machine with a 60 mm screw diameter and L/D 24:1 produces a parison at 205°C that is subsequently inflated in a mold chilled to 8°C. The melt–cooling mismatch is balanced so that the outer skin freezes to a thickness of 0.15 mm at the mold contact surface while the regrind layer flows to adhere to the EVOH core; a die swell ratio of 1.08:1 is maintained. The environmental stress cracking resistance (ESCR) of the structure, a critical parameter for surfactant packaging, is evaluated with a notched constant tensile load test in a 10% solution of nonylphenol ethoxylate at 50°C according to a modified ASTM D1693 method; the homopolymer-based system, when diluted with recycled content, exhibits an ESCR time to failure of >500 h, provided that the melt viscosity of the regrind fraction does not deviate more than 20% from virgin as determined by dynamic rheology at 0.1 rad/s. Food-contact approval for the multi-layer construction follows the functional barrier doctrine set out in Article 13 of Regulation (EC) No 1935/2004, with migration testing performed on the finished article at 40°C for 10 days using simulant A (10% ethanol) and demonstrating specific migration of maleic anhydride below the detection limit of 0.01 mg/kg. The terminal articles are screw-capped bottles for household cleaning concentrates and diluted disinfectants, with a drop-impact resistance specification requiring no rupture when dropped from 1.2 m at −18°C after conditioning for 24 h. A written manufacturing instruction prohibits shut-down of the extruder at temperature without purging the barrel with a low-MFR washgrade; static heating of H2000 under zero flow for more than 15 minutes rapidly leads to crosslinking gel formation that subsequently dislodges and contaminates the parison surface with visible specks.

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    Certification & Compliance
    More Introduction

    Exelene PP Homopolymer H2000 is a general-purpose polypropylene homopolymer grade engineered for injection moulding applications requiring a balance of stiffness, heat resistance and rapid cycle times. The resin is manufactured via bulk-phase polymerisation with a controlled isotacticity index that yields a narrow molecular weight distribution, enabling consistent melt viscosity under high shear. Typical melt mass-flow rate (MFR), measured at 230 °C under 2.16 kg load per ISO 1133-1:2022, falls in the 2.0 g/10 min range, positioning the material for medium-flow moulds where gate freeze-off must be delayed sufficiently to allow packing pressure transmission without sacrificing crystallisation speed. Density at 23 °C is 0.905 g/cm³ (ISO 1183-1), placing it in the conventional homopolymer band typified by PP grade designation PPH10 under ISO 1873-2 and ASTM D4101 Group 01, Class 1. The absence of ethylene comonomer confers higher crystalline melting temperature, measured by DSC at 160–165 °C, compared to random copolymers, while the controlled rheology minimises the draw-down thinning variation observed in broad-MWD reactor grades during high-speed injection.

    In high-cavitation tools running thin-wall containers, the H2000 grade demonstrates spiral flow lengths exceeding 90 cm at 255 °C melt temperature and 80 MPa injection pressure, tested on an Arburg Allrounder 470 E with a 25 mm screw and L/D 22. This behaviour reduces the in-mould crystallisation gradient between gate and end-of-fill, decreasing post-mould warpage variance to below ±0.15 mm on a 150 mm lid. The narrow molecular weight distribution, with polydispersity index below 3.8 as determined by gel permeation chromatography, yields a flat viscosity curve above 100 s⁻¹, meaning shear rate sensitivity is predictable across gate diameters from 0.5 mm to 2.0 mm. Consequently, backpressure settings on reciprocating screws can be held constant regardless of shot size variation within a family mould, a processing advantage not replicated with many impact copolymers that exhibit greater shear-thinning dependence on average molecular weight.

    Table 1 – Typical physical and mechanical properties of Exelene PP Homopolymer H2000
    PropertyTest MethodTypical ValueUnit
    Melt mass-flow rate (MFR)ISO 1133-1 (230 °C/2.16 kg)2.0g/10 min
    DensityISO 1183-10.905g/cm³
    Tensile stress at yieldISO 527-2 (Type 1A, 50 mm/min)34MPa
    Tensile elongation at yieldISO 527-29%
    Flexural modulusISO 178 (2 mm/min)1450MPa
    Notched Izod impact strength (23 °C)ISO 180/A2.5kJ/m²
    Notched Izod impact strength (−20 °C)ISO 180/A1.2kJ/m²
    Vicat softening temperature (A50)ISO 306154°C
    Heat deflection temperature (HDT, 0.455 MPa)ISO 75-2/B98°C
    Rockwell hardness (R-scale)ISO 2039-295

    Exelene H2000 in Conflict with High-Cycle Tooling: Gate Design and Crystallisation Pressure

    A recurring failure mode on 24-cavity hot-runner systems stacking this grade emerges when the gate diameter is below 0.8 mm and the cooling time is pushed under 3.5 seconds to achieve cycle times below 5.0 seconds. Under these conditions, the combination of high crystallisation rate inherent to homopolymer and the rapid melt solidification at the gate creates an effective backflow seal before holding pressure can fully compensate for volumetric shrinkage. Parts ejected from cavities farthest from the sprue exhibit sink marks deeper than 0.08 mm, exceeding dimension tolerances required by ISO 2768-1 class m. Raising melt temperature above 265 °C to reduce gate freeze-off time, however, induces thermo-oxidative degradation that shifts MFR upwards by 0.4–0.7 g/10 min within three residence time cycles, detectable by a yellowing index increase of ΔYI > 1.2 according to ASTM E313. Production lines that installed melt pressure transducers at each nozzle confirm that the critical shear stress limit of 0.14 MPa in the gate land must not be exceeded, otherwise molecular orientation in the skin layer drives anisotropic shrinkage sufficient to warp flat surfaces by 0.3° of curvature. This narrow processing window — typically ±3 °C on the melt temperature setpoint — is a direct consequence of the grade’s low yield of long-chain branching, a characteristic differentiating it from high-melt-strength homopolymers designed for thermoforming where extensional viscosity under transient flow is substantially higher.

    How Does H2000 Differ from Random Copolymer Grades in Regulated Food-Contact Articles?

    Unlike propylene-ethylene random copolymers with comonomer content of 2–4 wt%, H2000 contains no intentionally incorporated ethylene, which eliminates the possibility of extractable amorphous ethylene-rich fractions migrating into fatty food simulants. Migration testing under EU Regulation 10/2011 simulant D2 (vegetable oil) at 40 °C for 10 days returns an overall migration limit below 2.0 mg/dm², comfortably within the 10 mg/dm² statutory ceiling. The higher crystallinity of the homopolymer — measured by DSC enthalpy > 90 J/g — reduces the diffusion coefficient of Irganox 1010 antioxidant (Ciba, now BASF) by approximately 30 % compared to random copolymer matrixes, as validated by kinetic extraction studies in 95 % ethanol at 60 °C. However, this same crystalline barrier manifests in diminished cold-weather impact resistance: notched Izod at −20 °C drops to 1.2 kJ/m², whereas a standard random copolymer typically retains above 4.0 kJ/m². Processors switching from random to homopolymer for thin-wall food tubs must therefore accept a trade-off between extraction resistance and drop-impact robustness. Moulds originally designed for random copolymer often require a minimum radius of 1.5 mm at the rim to prevent brittle fracture, whereas random copolymer parts tolerated 0.8 mm radii without cracking.

    Pre-drying recommendations: while homopolymer polypropylene is not hydrolytically sensitive, melt phase moisture content above 0.1 wt% can generate steam that vaporises at the screw metering zone, causing surging and inconsistent shot weight. On extruders with vented barrels (L/D 28–32), no pre-drying is necessary, but for non-vented machines operating in ambient relative humidity exceeding 60 %, a dehumidifying dryer set to 80 °C for 2 hours is advised. Resin stored in open silos during monsoon seasons in Southeast Asia has exhibited moisture sorption sufficient to increase screw recovery time by 0.3–0.5 s per shot, attributed to vapour-phase pressure pulses inside the check ring assembly. This behaviour is specific to the H2000 grade’s narrow MWD, which produces a sharp viscosity drop at the vaporisation point—broad-MWD homopolymers tend to dampen such pressure transients more effectively due to their higher melt elasticity.

    Table 2 – Property contrast: Exelene PP Homopolymer H2000 vs. typical random copolymer and impact copolymer grades
    CharacteristicH2000 (homopolymer)Random copolymer (2–4 w% C₂)Impact copolymer (6–12 w% C₂)
    MFR, g/10 min (230 °C/2.16 kg)2.02.01.8
    Flexural modulus, MPa145010501250
    Notched Izod (−20 °C), kJ/m²1.24.58.0
    Vicat A50, °C154136148
    Haze, % (2 mm plaque)401560 (opaque)
    Gate freeze-off time (relative, 1 mm gate)1.0×1.3×1.1×
    Extractable fraction in hexane, %0.30.90.5
    Typical regulatory complianceFDA 21 CFR 177.1520, EU 10/2011FDA 21 CFR 177.1520, EU 10/2011FDA 21 CFR 177.1520 (with limitations)

    When dry-blended with calcium carbonate masterbatch up to 20 wt% filler loading on the hopper, H2000 exhibits less MFR drift than impact copolymers because the higher melt temperature required for dispersion does not degrade the matrix at the same rate. On a 75-tonne clamping force injection moulding machine with a 30 mm screw, a 20 wt% talc-filled compound based on H2000 maintained MFR within ±0.15 g/10 min over 200 hot cycles, whereas an impact copolymer base exhibited a MFR shift of +1.1 g/10 min under identical conditions. The homopolymer backbone’s absence of ethylene segments sterically hinders the abstraction of tertiary hydrogen atoms that triggers β-scission chain scission, a mechanistic difference confirmed by thermo-gravimetric analysis coupled with Fourier-transform infrared spectroscopy (TGA-FTIR) showing delayed propanal evolution.

    When Silo Storage and Pneumatic Conveying Induce Fines Segregation in the H2000 Pellet Stream

    Pneumatic systems operating at conveying velocities exceeding 25 m/s can generate fines fractions above 150 ppm due to pellet-to-pipe wall attrition of the homopolymer’s relatively brittle surface, which is Shore D 70 hardness. These fines, enriched in low-molecular-weight crystalline platelets, segregate in the hopper and create local viscosity minima leading to short shots on starved-feed machines. Optical microscopy of sieved fractions reveals plate-like fragments 50–80 μm in length, which melt prematurely in the feed throat and coat the screw root, reducing forward conveying efficiency. A remedy adopted in multi-hopper lines is the installation of a cyclone deduster that reduces fines to below 30 ppm before loading; without such intervention, shot weight coefficient of variation exceeds 1.5%. This operational artefact is far less pronounced in impact copolymer grades due to the elastomeric domains absorbing impact energy during conveying.

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