| HS Code | 543064 |
| Polymer Type | Polypropylene (PP) |
| Density | 0.905 g/cm³ |
| Melting Point | 160–170 °C |
| Glass Transition Temperature | -20 to 0 °C |
| Crystallinity | 40–70% |
| Tensile Strength | 20–40 MPa |
| Elongation At Break | 100–600% |
| Flexural Modulus | 0.9–1.5 GPa |
| Notched Izod Impact Strength | 20–100 J/m |
| Hardness | Rockwell R80–R110 |
| Thermal Conductivity | 0.1–0.22 W/m·K |
| Specific Heat Capacity | 1.7–1.9 J/g·K |
| Water Absorption | <0.02% |
| Dielectric Constant | 2.2–2.6 at 1 MHz |
| Chemical Resistance | Good resistance to acids, bases, alcohols, and most solvents; poor resistance to chlorinated solvents and strong oxidizers |
| Uv Resistance | Poor unless stabilized |
| Flammability | Flammable; UL 94 HB typical |
| Processing Temperature | 200–280 °C |
| Mold Shrinkage | 1.0–2.5% |
| Continuous Service Temperature | -20 to 100 °C |
As an accredited Polypropylene PP factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Polypropylene (PP) supplied in 25 kg sealed woven bags, stacked on pallets and wrapped for safe industrial transport. |
| Container Loading (20′ FCL) | Polypropylene PP loaded in 20′ FCL: palletized 25 kg bags, dry container, uniform weight distribution, secure stowage, non-hazardous. |
| Shipping | Polypropylene (PP) is generally non-hazardous and shipped as pellets, granules, or powder in 25 kg bags, bulk bags, octabins, or bulk truck/rail containers. Keep dry, clean, away from ignition sources and UV. No special DOT/IMDG labeling usually required; follow manufacturer SDS and local regulations. |
| Storage | Store Polypropylene (PP) at ambient temperature in a cool, dry, well-ventilated area away from direct sunlight, heat, flames, and strong oxidizers. Keep in sealed, labeled containers or original packaging to prevent moisture, dust, and contamination. Avoid prolonged UV exposure. Use grounding and bonding to control static during handling. Maintain good housekeeping and clean spills promptly to prevent slipping hazards. |
| Shelf Life | Polypropylene (PP) has an indefinite shelf life when stored properly in a cool, dry, dark place, away from UV and heat. |
In plants feeding high-aspect-ratio twin-screw extruders with 40–64 L/D configuration and segmented kneading blocks, polypropylene impact copolymer resin with a melt flow rate of 20–35 g/10 min at 230 °C/2.16 kg per ISO 1133-1:2022 is compounded with ethylene-propylene-diene monomer rubber or metallocene polyolefin elastomer at 18–28 wt% and stearate-coated talc at 12–22 wt% to produce a thermoplastic polyolefin for injection-molded automotive exterior and semi-structural interior components. The formulated compound typically contains a hindered phenolic/phosphite antioxidant package at 0.2–0.4 wt%, a hindered amine light stabilizer package at 0.1–0.3 wt%, and carbon black masterbatch at 1–2 wt% where exterior UV performance is specified. Material compliance for interior parts is evaluated against VDA 278:2011 thermodesorption analysis of volatile and semi-volatile organic compounds, and for exterior parts against EU Directive 2000/53/EC end-of-life vehicle restrictions and REACH Annex XVII substance restrictions. Mechanical acceptance is anchored to ISO 178:2019 flexural modulus, ISO 179-1 Charpy notched impact, ISO 180 Izod impact, and ASTM D3763 multi-axial puncture resistance. Compounding on a 40–64 L/D twin-screw line is carried out with barrel set-points from 180 °C in the rear feed zone to 230 °C in the front kneading section and melt discharge held below 250 °C; production-scale lines running above 260 °C exhibit ethylene-phase degradation, screw char deposition, and batch-to-batch notched impact drift of more than 15%. Injection molding of the compounded granulate into bumper fascia and instrument panel carriers typically uses a melt temperature of 230–250 °C, a mold temperature of 30–50 °C, injection pressure of 80–120 MPa, and clamp forces between 7,000 kN and 20,000 kN depending on projected part area. The terminal component set includes bumper fascia, body side cladding, instrument panel carriers, door panel substrates, glove box housings, and airbag cover backings. Talc loading above 22 wt% is a defined cliff-edge variable; at −30 °C the multi-axial impact energy per ASTM D3763 can move from a ductile plateau near 15–18 J at 10–15 wt% talc to a brittle failure mode below 6 J when the filler network restricts elastomer ligament deformation and the interparticle spacing falls below the critical stress-whitening propagation length. The property transition across filler loading is reported in the following table for a 20 wt% elastomer baseline.
| Talc loading (wt%) | Flexural modulus, ISO 178:2019 (MPa) | Notched Charpy impact at −30 °C, ISO 179-1 (kJ/m²) | Melt flow rate, ISO 1133-1:2022 (g/10 min) |
|---|---|---|---|
| 0–5 | 1,100–1,400 | 14–18 | 22–28 |
| 10–15 | 1,600–2,100 | 10–14 | 20–25 |
| 20–25 | 2,400–3,000 | 5–9 | 18–24 |
| 30–35 | 3,300–4,000 | 2–5 | 15–20 |
On production meltblown lines, polypropylene homopolymer with controlled rheology and a melt flow rate of 800–1,500 g/10 min per ISO 1133-1:2022 is extruded through a row of spinneret holes with diameters between 0.15 mm and 0.25 mm, while high-velocity hot air at 270–320 °C attenuates the melt into fibers of 0.5–5 µm diameter before collection on a vacuum conveyor drum at a die-to-collector distance of 150–300 mm. Compliance for surgical face masks and respirators is evaluated under EN 14683:2019+AC:2019 and ASTM F2100-23; media intended for medical device construction must be evaluated under ISO 10993-1:2018 for cytotoxicity, sensitization, and irritation, while food-contact nonwovens fall under FDA 21 CFR 177.1520 and EU Regulation 10/2011 where applicable. Formulation for spunbond layers uses MFR 25–40 g/10 min, with 0.05–0.15 wt% erucamide slip additive, 0.05–0.15 wt% hindered phenolic antioxidant, and 0.02–0.05 wt% phosphite processing stabilizer; meltblown layers typically retain the antioxidant package but omit slip additive to avoid surface contamination that depresses electrostatic charging. Spunbond production uses a single-screw extruder, melt pump, spinneret hole diameters of 0.3–0.6 mm, quench air at 20–26 °C, filament draw velocities of 3,000–5,000 m/min, and inline thermal calendering at 130–150 °C with nip pressures of 50–90 N/mm to consolidate the web. Electret charging is performed by corona discharge at 40–80 kV or by hydro-charging, and the charged web must maintain bacterial filtration efficiency of at least 98% for Type IIR face masks per EN 14683:2019+AC:2019 after accelerated aging at 25 °C/80% RH for 24 h; uncharged or charge-decayed media below 20 g/m² typically do not provide consistent submicron aerosol capture at 85 L/min challenge flow. Production-scale failure modes include shot and roping defects when the melt filter screen pack is coarser than 40–60 µm, and melt flow rate drift of ±10% in peroxide-cracked resin alters fiber diameter distribution enough to shift pressure drop and filtration efficiency beyond the limits specified in EN 14683:2019+AC:2019. Terminal products include spunbond-meltblown-spunbond surgical masks, respirator filtration layers, air filtration pleat media, hygiene acquisition distribution layers, and sterile barrier overlays.
Sequential tenter-frame lines processing polypropylene homopolymer with an isotacticity index above 96% and MFR of 2.0–4.0 g/10 min per ISO 1133-1:2022 into 15–40 µm biaxially oriented film operate with a chill roll temperature of 20–30 °C, a longitudinal stretching ratio of 4.5:1–5.5:1 at 125–145 °C, and a transverse stretching ratio of 7.0:1–9.0:1 at 155–170 °C, followed by annealing at 160–170 °C with 2–8% relaxation to control longitudinal shrinkage. Food-contact films are evaluated under EU Regulation (EC) No 1935/2004, EU Regulation 10/2011 as amended, and FDA 21 CFR 177.1520; printing and lamination grades additionally require surface tension after corona treatment between 38 mN/m and 44 mN/m measured per ASTM D2578, while optical haze is controlled under ASTM D1003 and coefficient of friction under ASTM D1894. Core-layer formulation is based on 100 parts by mass PP homopolymer with 0.03–0.08 wt% acid neutralizer; skin layers contain propylene-ethylene random copolymer or terpolymer at 70–90 wt%, erucamide slip additive at 0.05–0.12 wt%, synthetic amorphous silica antiblock at 0.08–0.20 wt%, and glycerol monostearate antistatic at 0.2–0.6 wt% depending on print and winding requirements. Downstream converting includes slitting, corona discharge, vacuum metallization for barrier films, and adhesive lamination. Terminal product types include snack food wrappers, biscuit bags, label face stock, adhesive tape base film, tobacco overwrap, and metallized barrier pouches. Slip additive migration is time-temperature dependent; coefficient of friction may remain above 0.35 for 24 h at 23 °C but fall below 0.25 after 72 h at 35 °C. If erucamide exceeds 0.15 wt% in the skin layer, plate-out accumulates on transverse-direction oven nozzles and chill roll pinholes increase; if the antiblock content is below 0.08 wt%, film-to-film blocking during rewind storage leads to telescoping and web breaks at converting speeds above 400 m/min.
Polypropylene impact copolymers selected for radiation-sterilized medical components are compounded with an ethylene content of 2–6 wt%, a hindered phenolic antioxidant at 0.08–0.15 wt%, a phosphite at 0.05–0.10 wt%, an acid neutralizer at 0.03–0.08 wt%, and a sorbitol-based clarifier at 0.15–0.25 wt% to stabilize morphology and limit post-irradiation yellowing. Regulatory compliance is evaluated under ISO 10993-1:2018, ISO 10993-5 for cytotoxicity, ISO 10993-10:2021 for sensitization, USP <88> Class VI, Ph. Eur. 3.1.3, and FDA 21 CFR 177.1520 for polymer construction and food-contact migration when relevant. Parts are injection molded at melt temperature 210–240 °C, mold temperature 10–30 °C, injection pressure 100–140 MPa, holding pressure 60–80 MPa, and hot runner valve gates to maintain dimensional tolerances of ±0.1 mm on syringe bore features. Pre-drying at 80 °C for 2 h is required when ambient relative humidity exceeds 60% to prevent surface splay caused by moisture absorbed in granulate storage. Radiation sterilization at 25–40 kGy is preferred; doses above 40 kGy induce measurable embrittlement through oxidative chain scission, with Charpy notched impact declining by more than 30% and yellowness index increasing beyond 2 units. Ethylene oxide processing at 45–55 °C may be used for temperature-sensitive assemblies but requires aeration to remove residual ethylene oxide below the limit specified in ISO 10993-7; steam sterilization at 134 °C is generally not suitable for standard PP components because of softening and dimensional distortion, while limited exposure at 121 °C may be tolerated only with fixture support and designed clearances. Extractable profiles per USP <661.1> and ISO 10993-12 are monitored to ensure that total organic carbon and antioxidant-derived leachables remain below the monograph thresholds for the intended route and duration; published data for this specific formulation configuration is limited, but the absence of amide slip additives and the low phenolic loading are designed to keep non-volatile residue below the compendial limit. Terminal product types include syringe barrels, plunger rods, specimen containers, IV catheter hubs, inhaler bodies, and laboratory pipette tips.
PP-R random copolymer pipe compounds are formulated with an ethylene content of 2.5–3.5 wt% and a melt flow rate of 0.25–0.50 g/10 min per ISO 1133-1:2022 to balance slow crack growth resistance with extrusion output. Pipe and fittings are specified under ISO 15874-1:2013 and ISO 15874-2:2013; long-term hydrostatic strength is evaluated by the reference curve procedure of ISO 9080, and potable-water contact in North America is certified under NSF/ANSI/CAN 61 and CSA B137.11, with EU contact regulated under EU Regulation 10/2011 and applicable national positive lists. Compound contains hindered phenolic antioxidant at 0.3–0.5 wt%, phosphite at 0.1–0.2 wt%, acid neutralizer at 0.05–0.10 wt%, and colorant or carbon black masterbatch at 0.5–2.0 wt% to ensure UV resistance and marking legibility. Extrusion uses a single-screw extruder with 30–34 L/D barrier screw, barrel profile from 190 °C in the feed section to 240 °C in the metering zone, melt temperature 200–230 °C, die temperature 200–220 °C, and vacuum calibration at −0.06 MPa to −0.08 MPa with water cooling at 20–35 °C. Pipe puller speed is adjusted to maintain wall thickness per ISO 3126 within +0.5 mm tolerance for dimensions up to 110 mm outer diameter. Socket fusion joining is performed at 260 °C with heating and cooling times derived from pipe wall thickness using the manufacturer temperature-time matrix. If melt temperature falls below 200 °C, output from the barrier screw becomes unstable, surface sharkskin defects appear on the outer surface, and un-melted gel bodies create notch points that lower hydrostatic burst pressure at 95 °C below the regression curve; production lines therefore override the barrel setpoint when melt pressure exceeds 25 MPa or die pressure fluctuation exceeds ±5%. Terminal products include potable hot and cold water risers, district heating distribution lines, radiator connection piping, low-pressure industrial compressed air lines, and chemical drainage pipe for corrosive effluent.
Manufacture of 2–12 µm polypropylene dielectric film begins with an ultra-clean PP homopolymer having isotacticity above 95%, melt flow rate of 2.0–3.5 g/10 min, residual catalytic ash below 30 ppm, and chlorine content below 5 ppm to limit the concentration of ionic conduction sites that reduce dielectric breakdown strength. Electrical film is specified under IEC 60674-3-3, with dielectric strength evaluated per ASTM D149 and dielectric constant and dissipation factor per ASTM D150; complete film capacitors are assessed under IEC 60384-1 and application-specific sectional specifications such as IEC 61071 for power electronic capacitors. Compliance with RoHS Directive 2011/65/EU and REACH is required for electrical and electronic equipment placed on the EU market. Formulation includes 0.03–0.08 wt% hindered phenolic antioxidant and 0.01–0.03 wt% acid neutralizer; no slip, antiblock, antistatic, or clarifying additives are permitted because they increase ash or surface contamination and depress capacitor winding performance. The melt is filtered through a 10–20 µm sintered metal screen pack to remove gel particles above 20 µm, cast onto a chill roll at 20–35 °C to minimize spherulite size, then biaxially oriented sequentially at longitudinal ratio 4.0:1–5.5:1 and transverse ratio 8.0:1–10.0:1 at temperatures between 130 °C and 170 °C. The biaxially oriented film is vacuum-metallized with aluminum or zinc at a thickness of 10–30 nm and sheet resistance of 2–5 Ω/sq, then slit and wound into capacitor-grade reels under cleanroom conditions with air particle count below 1,000 particles/ft³ of size 0.5 µm or larger. Surface gel particles larger than 30 µm create pinholes during metallizing that register as instantaneous breakdown faults, while ash above 30 ppm reduces dielectric strength per IEC 60674-3-3 below the commonly accepted 200 V/µm lower control limit for high-voltage direct-current capacitor film. Production-scale rewind equipment therefore uses in-line defect detection with optical sensors at 5–10 m/s line speed to reject rolls with more than 10 pinholes/m². Terminal products include DC-link capacitors in electric vehicle inverters, motor-run capacitors, power factor correction capacitors, and surface-mount film capacitors in switch-mode power supplies.
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Polypropylene PP comprises a family of semicrystalline thermoplastic olefin homopolymers and copolymers designated PP-H, PP-B, and PP-R under ISO 1873-1 and ISO 19069-1. Specification sheets distinguish these families by melt flow rate measured at 230 °C with a 2.16 kg load according to ISO 1133-1:2022, with commercial MFR values from 0.3 g/10 min for thick sheet extrusion to 100 g/10 min for high-speed injection molding. Isotactic homopolymer density is 0.900–0.910 g/cm³ per ISO 1183-1; random copolymer grades range from 0.897 g/cm³ to 0.905 g/cm³; impact copolymer grades sit between 0.895 g/cm³ and 0.905 g/cm³. Differential scanning calorimetry per ISO 11357-3 shows peak melting endotherms at 160–168 °C, with crystallization onset typically 115–125 °C in unfilled resins.
Representative product configurations include PP-H MFR 3, 12, 25, and 50 g/10 min for injection molding; PP-R MFR 2–35 g/10 min for cast film, medical articles, and heat-sealable packaging; PP-B MFR 4–44 g/10 min for automotive interior trims, cold-chain packaging, and impact-modified closures. Designation blocks also record tensile modulus, impact strength, and processing shrinkage, which are specified through the test methods in the table below.
Melt flow rate functions as an inverse indicator of average molar mass. Raising MFR from 12 g/10 min to 50 g/10 min reduces cycle time in thin-wall molding but lowers notched Charpy impact at 23 °C from approximately 4 kJ/m² to 2 kJ/m² when measured by ISO 179-1/1eA. The trade-off is governed by chain entanglement and spherulite size. Impact copolymer grades interrupt the crystalline homopolymer matrix with ethylene-propylene rubber domains of 0.2–2.0 µm average particle size, raising −20 °C impact energy to 5–15 kJ/m². Random copolymer introduction of 2.5–4.5 wt% ethylene lowers crystallinity, reduces flexural modulus, and depresses seal-initiation temperature, but also lowers 0.45 MPa heat deflection temperature compared with PP-H. The resulting property profile is therefore a deliberate gradient from stiff homopolymer to tough impact copolymer.
| Property | Test method | PP-H homopolymer | PP-R random copolymer | PP-B impact copolymer |
|---|---|---|---|---|
| Density | ISO 1183-1 | 0.900–0.910 g/cm³ | 0.897–0.905 g/cm³ | 0.895–0.905 g/cm³ |
| Melt flow rate | ISO 1133-1:2022 at 230 °C/2.16 kg | 0.3–100 g/10 min | 2–35 g/10 min | 4–44 g/10 min |
| Tensile yield stress | ISO 527-2 | 25–40 MPa | 20–30 MPa | 18–30 MPa |
| Elongation at break | ISO 527-2 | 100–600% | 300–500% | 200–600% |
| Flexural modulus | ISO 178 | 1100–1600 MPa | 800–1200 MPa | 900–1300 MPa |
| Notched Charpy impact, 23 °C | ISO 179-1/1eA | 2–5 kJ/m² | 5–15 kJ/m² | 10–40 kJ/m² |
| Notched Charpy impact, -20 °C | ISO 179-1/1eA | 1–2 kJ/m² | 1.5–3 kJ/m² | 5–15 kJ/m² |
| Heat deflection temperature, 0.45 MPa | ISO 75-2/B | 90–110 °C | 75–95 °C | 85–105 °C |
| Vicat softening temperature, A50 | ISO 306 | 150–155 °C | 140–150 °C | 140–150 °C |
| Mold shrinkage | ISO 294-4 | 0.010–0.025 mm/mm | 0.010–0.020 mm/mm | 0.010–0.025 mm/mm |
Injection molding of PP-H and PP-B grades is performed on reciprocating-screw machines with screw L/D ratios of 20:1 to 24:1 and compression ratios from 2.0:1 to 3.0:1. Barrel set points are typically 200–260 °C, with mold temperature maintained at 20–60 °C for homopolymer and 30–70 °C for impact copolymer to control crystallization rate and post-mold shrinkage. Thin-wall packaging grades with MFR 50–100 g/10 min are processed in multi-cavity hot-runner tools under injection pressures of 80–140 MPa; projected-area clamp force is generally set at 2.5–5.0 kN/cm². Processing conflicts arise when mold temperature deviates more than ±5 °C because part weight and dimensions shift through altered crystallization half-time. For multi-cavity lids and closures, a mold temperature increase from 20 °C to 40 °C can increase mold shrinkage by 0.003–0.005 mm/mm, enough to compromise seal dimensions.
Cast film extrusion of PP-R uses melt temperatures of 220–250 °C and chill-roll temperatures of 15–30 °C. Heat-seal initiation for PP-R with 2.5–4.5 wt% ethylene comonomer is typically reported at 118–128 °C when measured by ASTM F2029-16. Biaxially oriented PP film is produced on tenter-frame lines with longitudinal stretching at 130–145 °C and transverse stretching at 145–160 °C; transverse temperature uniformity is commonly held within ±3 °C to avoid gauge variation or bubble break. Published data for specific high-speed stenter configurations is limited, but equipment manufacturers recommend longitudinal draw ratios of 4.5:1 to 5.5:1 followed by transverse draw ratios of 8:1 to 10:1 for balanced tensile properties.
Spunbond nonwoven production uses PP-H with MFR 25–60 g/10 min, melt temperature 220–240 °C, and high-shear screw elements for melt homogeneity. Fiber-grade formulations include slip and nucleating packages because the narrow residence-time distribution in spunbond lines makes melt-temperature excursions beyond 240 °C particularly damaging to molecular weight retention. Unfilled PP is hydrophobic and does not require pre-drying under normal storage below 60% relative humidity; however, talc-filled or calcium-carbonate-filled compounds can accumulate surface moisture and are often dried at 80–90 °C for 2–4 h when loaded with hygroscopic functional additives.
Compounds containing 10–20 wt% talc raise flexural modulus to 1800–2500 MPa per ISO 178 and increase heat deflection temperature at 1.8 MPa to 65–90 °C per ISO 75-2/A. These materials are produced on twin-screw extruders with L/D ratios from 40:1 to 44:1, using downstream side-feeding of mineral filler to limit barrel wear. Replacement of ABS in interior trim requires attention to thermal expansion differences: unfilled PP exhibits CLTE of 100–150 × 10⁻⁶ K⁻¹, talc-filled PP 60–90 × 10⁻⁶ K⁻¹, and ABS approximately 70–90 × 10⁻⁶ K⁻¹ when measured by ISO 11359-2. The mechanical limitation is low-temperature toughness. Notched Izod impact per ISO 180/A for talc-filled PP-B can remain above 8 kJ/m² at 23 °C but may fall below 4 kJ/m² at -30 °C, whereas ABS frequently retains 10–20 kJ/m² under the same condition. Semi-structural substitution is therefore confined to upper interior trim, console substrates, and underhood covers where ductile failure at subzero temperatures is not safety-critical.
Polypropylene occupies a density range of 0.895–0.910 g/cm³, compared with HDPE at 0.940–0.965 g/cm³, PET at 1.30–1.40 g/cm³, and rigid PVC at 1.35–1.45 g/cm³. Its flexural modulus of 1100–1600 MPa for unfilled PP-H exceeds HDPE at 800–1200 MPa but remains below PET and rigid PVC at 2000–3000 MPa. Low-temperature ductility differentiates the olefins: PP-H records notched Charpy at -20 °C of 1–2 kJ/m², whereas HDPE retains 4–10 kJ/m²; PP-B impact copolymer narrows the gap to 5–15 kJ/m². Barrier selectivity is reversed for oxygen and moisture. Oxygen permeation at 23 °C, 0% RH is approximately 50–100 cm³·mm/(m²·day·bar) for PP under ASTM D3985, while PET is near 1–3 cm³·mm/(m²·day·bar). Water vapor transmission at 38 °C, 90% RH measured by ASTM F1249 is typically lower in PP than in PET, which supports PP selection for moisture-barrier packaging despite weaker oxygen barrier. Chemical resistance follows ASTM D543-21 or ISO 22088-1: unfilled PP withstands 10–30% aqueous acids and alkalies at ambient temperature but swells in aromatic hydrocarbons, chlorinated solvents, and high-octane fuels. Thus PP is selected where stiffness-to-density ratio and moisture tolerance are more important than oxygen barrier or high-load heat resistance.
For regulated packaging and medical applications, PP grades are supplied with compliance documentation citing FDA 21 CFR 177.1520 for olefin polymers, USP Class VI or ISO 10993-5 for cytotoxicity. REACH and RoHS declarations are standard for unfilled and common mineral-filled grades, although pigment-bound heavy metals require verification against IEC 62321 methods. Continuous dry heat exposure above 100 °C without stabilizer packages leads to oxidative embrittlement within months; copper ion contamination accelerates thermo-oxidative chain scission and is avoided in hot-water piping compounds by using stabilizer systems validated by long-term hydrostatic testing per ISO 9080 at 95 °C. Unfilled PP is not recommended for prolonged service in contact with strong oxidizing acids or aromatic solvents, and UV-stabilized grades should be specified for outdoor weatherability according to ISO 4892-2 accelerated exposure protocols.