Ningxia Baofeng Energy Group Co., Ltd

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Polypropylene Homopolymer PP S1003G

    • Product Name: Polypropylene Homopolymer PP S1003G
    • Factroy Site: Ningdong Energy and Chemical Industry Base, Yinchuan City, Ningxia
    • Price Inquiry: sales4@liwei-chem.com
    • Manufacturer: Ningxia Baofeng Energy Group Co., Ltd
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    Specifications
    HS Code 572050
    Density 0.90 g/cm³
    Melt Flow Rate 230c 2 16kg 3.0 g/10 min
    Tensile Strength At Yield 30 MPa
    Elongation At Break 15%
    Flexural Modulus 1200 MPa
    Notched Izod Impact Strength 23c 30 J/m
    Heat Deflection Temperature 0 45mpa 100 °C
    Vicat Softening Temperature 150 °C
    Rockwell Hardness R90
    Molding Shrinkage 1.0–2.0%
    Ash Content ≤0.02%
    Isotacticity ≥95%
    Yellow Index ≤4
    Moisture Content ≤0.05%
    Melting Temperature 160–170 °C

    As an accredited Polypropylene Homopolymer PP S1003G factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Polypropylene Homopolymer PP S1003G is supplied in 25 kg PP woven bags with PE liners, 40 bags per pallet (1,000 kg).
    Container Loading (20′ FCL) Container Loading (20′ FCL): Polypropylene Homopolymer PP S1003G packed in 25 kg bags, loaded into a 20-foot FCL, securely stowed and sealed.
    Shipping Polypropylene Homopolymer PP S1003G is a non-hazardous polymer resin shipped as solid pellets in 25 kg bags or 1,000 kg jumbo bags. Transport in dry, clean containers by sea, road, or rail. Store in a cool, dry, ventilated area, protected from moisture, direct sunlight, and ignition sources.
    Storage Store Polypropylene Homopolymer PP S1003G in a cool, dry, well-ventilated area away from direct sunlight, heat, and ignition sources. Keep original containers closed and palletized to prevent moisture, dirt, and UV degradation. Avoid contact with strong oxidizing agents. Maintain stable temperature, prevent static buildup, follow local fire regulations, and handle pellets carefully to minimize dust generation.
    Shelf Life Typically 24 months when stored in a cool, dry, well-ventilated area, away from direct sunlight, heat, and moisture.
    Application of Polypropylene Homopolymer PP S1003G

    Across a sequential biaxial stretching line, the homopolymer PP grade S1003G is processed as the core layer of a three-layer BOPP film, with a melt-mass flow rate of 3.0 g/10 min determined under ISO 1133-1:2022 at 230 °C and 2.16 kg load. The cast sheet is extruded at 230–260 °C through a T-die with a die gap of 1.8–2.4 mm, quenched on a chill roll maintained at 30–40 °C, and reconditioned in a longitudinal stretching unit where surface temperature is held at 155–165 °C. Machine-direction draw is limited to 4.5:1–5.5:1; transverse-direction draw in the tenter frame is set at 7:1–9:1. The lower temperature boundary is not a conservative margin: below 152 °C the transverse drawing section exhibits microvoiding and edge tear propagation because the amorphous tie-chain fraction in a 3.0 MFR homopolymer cannot redistribute stress across the web. Above 168 °C, lamellar thickening raises haze above 2.0 % when tested under ASTM D1003-21 and reduces corona treatment stability measured by wetting tension under ASTM D2578-23.

    Formulation control on a production biax line using S1003G as the core resin is typically structured around 96.0–99.5 wt% base pellet, 0.5–2.0 wt% antiblock masterbatch based on 20 % synthetic silica, equating to an active silica concentration of 0.10–0.40 wt%, 0.05–0.15 wt% erucamide slip additive, and 0.05–0.20 wt% amine-free antistatic concentrate. Published BOPP conversion data for this exact S1003G configuration remain limited; the ranges above are derived from industrial biax lines running 3.0 MFR homopolymer grades with similar isotactic index. For direct food-contact constructions, the coextruded film complies with FDA 21 CFR 177.1520 and EU Regulation (EU) No 10/2011 Annex I, subject to an overall migration limit of 10 mg/dm² under the specified test conditions of Annex III. Because single-layer S1003G does not provide a heat-seal initiation temperature below 135 °C, food packaging converters coextrude random copolymer PP skins with a seal initiation temperature of 105–115 °C to produce 15–40 µm rollstock for snack pouches, confectionery twist wrap, bottle labels, tape backing, and transparent overwrap.

    Process variableLower operating limitUpper operating limitObserved failure at boundary
    MDO preheat surface temperature152 °C168 °CTD edge tears; haze > 2.0 %
    TD stretch ratio7:19:1Web sag below lower limit; edge tear above upper limit
    MD stretch ratio4.5:15.5:1Low stiffness below; film breakage above
    Corona wettability38 mN/m42 mN/mInk adhesion failure below; surface oxidation above

    Corona treatment on the tenter line is maintained at 38–42 mN/m wettability before winding; values below 36 mN/m lead to ink adhesion failure on CI flexographic presses, while values above 46 mN/m cause surface oxidation defects in the final film. Tensile properties of the oriented core are controlled by ASTM D882-18: machine-direction tensile strength is typically 120–160 MPa and transverse-direction tensile strength 250–300 MPa, with elongation at break 110–180 % in MD and 35–60 % in TD. The film edges are trimmed and fed back as in-house reclaim at not more than 15 wt% of the core layer because higher trim reload destabilizes the transverse stretch ratio and creates nonuniform thickness banding.

    Why Is the Water-Quench Temperature a Grade-Specific Control for S1003G Raffia Tape?

    The water-quench tank in raffia conversion is not merely a cooling stage; it fixes the skin-core morphology that determines whether S1003G tapes fibrillate under draw ratios of 5:1–8:1. The grade enters a single-screw extruder with L/D 30:1 at 200–250 °C, is extruded from a slit die with die gap 1.0–1.6 mm, and enters a water bath controlled at 25–40 °C. Air-knife dewatering removes surface water before the tape enters a hot-air stretching oven at 120–150 °C, followed by annealing rollers at 130–150 °C. Water-quench temperature below 20 °C produces a quenched skin too deep to orient uniformly; the core draws ahead of the skin and tape splitting initiates as longitudinal fibrillation at draw ratios above 5:1. Water-bath temperature above 45 °C slows surface crystallization and produces a translucent, low-tensile tape; subsequent woven fabric fails to maintain warp tensile strength above 750 N/50 mm when tested under ISO 13934-1:2013.

    Formulation is adjusted at the hopper with 2.0–8.0 wt% calcium carbonate masterbatch, 0.2–0.8 wt% hindered amine light stabilizer masterbatch at 10–20 % active concentration, and 0.5–1.0 wt% pigment concentrate. Filler addition above 8 wt% reduces tape elongation and causes loom-side dust accumulation; below 2 wt% the tape surface retains a high coefficient of friction that interferes with circular loom shuttle motion. For FIBC construction, the finished container is evaluated under ISO 21898:2004, which requires a minimum safety factor of 5:1 for single-trip bags and 6:1 for reusable designs; where dangerous goods transport is required, the bag must pass UN 13H2 design type testing. Food-contact woven sacks for rice, flour, and pulses are governed by FDA 21 CFR 177.1520 and EU Regulation (EU) No 10/2011, with special attention to total migration below 10 mg/dm² when the sack lacks an inner liner film.

    After stretching, the tape is annealed on heated godet rollers at 130–150 °C and wound on precision winders with tension control below 0.25 N/tape to prevent block shrinkage. Circular looms operate at 90–110 % of the tape width cover factor; fabric mass per unit area is set at 55–70 g/m² for standard woven sacks and 140–200 g/m² for FIBC body panels. The terminal converted forms include flat woven sacks, gusseted rice bags, leno-mesh bags for fresh produce, sandbags, carpet backing, and flexible intermediate bulk container panels. Outdoor-grade tape requires at least 48 h of QUV testing under ASTM G154-23 cycle 1 with no surface chalking; published data for S1003G under prolonged weathering beyond 500 h remains limited.

    On a 400-tonne hydraulic reciprocating screw injection molding machine, S1003G is metered to produce stackable crates, pails, and storage containers with nominal wall thickness of 1.2–3.5 mm. Barrel zones are set from 210 °C at the feed throat to 245 °C at the nozzle, screw back pressure is held at 5–10 MPa, and injection speed is adjusted to 60–150 mm/s depending on flow length from the gate. Holding pressure applied for 10–15 s is set at 50–80 MPa; mold temperature is maintained at 20–50 °C by a water thermoregulator. S1003G exhibits anisotropic mold shrinkage of 1.0–2.0 % in the flow direction and 0.8–1.5 % transverse to flow when measured under ASTM D955-21 on a 2 mm plaque. The low melt-mass flow rate of 3.0 g/10 min imposes an operational boundary: flow length to wall thickness ratios should not exceed 220:1; thin-wall packaging below 1.0 mm is generally not run with this grade because the pressure requirement at the screw tip exceeds 120 MPa and causes gate blush and short shots.

    Formulation in this rigid packaging sector is simple: 100 wt% S1003G may be used for translucent, non-colored crates, while colored pails and housewares use 1.0–3.0 wt% pigment masterbatch and 0.05–0.20 wt% external lubricant concentrate. Post-industrial regrind from sprues and rejected crates is introduced at 10–30 wt% when the part is non-food-contact; food-contact pails require same-source regrind per EU Regulation (EU) No 10/2011 Article 19 and FDA 21 CFR 177.1520. Impact failure remains the limiting property: notched Charpy impact strength under ISO 179-1/1eA at 23 °C remains in the range of 3.0–4.0 kJ/m², which excludes S1003G from drop-rated pails used for sub-zero storage unless the wall thickness is increased above 2.5 mm and the gate design is modified with a full-round sprue diameter of at least 6 mm. Although PP is not hygroscopic, surface moisture absorbed in high-humidity warehouses at RH above 60 % can produce splay defects; converters pre-dry pellets at 80 °C for 2 h in a desiccant dryer before processing.

    Terminal parts produced by this route are stackable vegetable crates, 5–20 L paint pails with UN open-head certification where hazardous liquid transport is required, storage bins, caps with living hinges for non-food use, and domestic housewares such as buckets and organizers. The process window is narrow: melt temperatures above 270 °C initiate thermo-oxidative chain scission as shown by a rise in melt flow rate; mold temperatures below 15 °C produce visible flow marks and unpredictable sink depth above 0.05 mm.

    When S1003G Is Drawn into Monofilament at a Stretch Ratio Below 7:1

    Monofilament converters processing S1003G through circular dies with hole diameters of 0.8–2.5 mm operate at melt temperatures of 220–260 °C and use a water quench at 25–35 °C. The quenched strand passes over a first godet at 10–30 m/min, enters a hot-water or hot-air stretching cabinet at 130–160 °C, and is drawn at ratios of 5:1–9:1 before relaxation of 5–10 % at 90–120 °C. At draw ratios below 7:1, the monofilament retains an undrawn core; the result is high elongation at break above 45 %, low modulus below 2.5 GPa under ISO 527-2:2012, and elevated creep that is unacceptable for load-carrying netting. Above 9:1, surface fibrillation and transverse microcracks appear, particularly when the first water quench is below 20 °C.

    Formulation for this downstream is low in particulate additives: 96–99 wt% S1003G, 0.3–1.2 wt% UV masterbatch containing 20 % hindered amine light stabilizer for outdoor ropes and agro nets, and 0.5–2.0 wt% color concentrate. Calcium carbonate is omitted because filler particles act as stress concentrators during stretching and reduce knot strength retention below 50 % when tested under ASTM D3218-07(2013). Geotextile-grade monofilaments are installed only if the manufacturer demonstrates long-term creep resistance according to ISO 13431:1999; published data for S1003G in geotextile service older than 5 years are limited, so design engineers impose a partial safety factor on tensile strength of 1.4–1.6. Export to the EU requires registration and notification compliance under REACH Regulation (EC) No 1907/2006 Article 33 when any added substance exceeds the SVHC threshold.

    Terminal uses include rope, baler twine, braided cordage, fishing-line monofilament, agro shade nets, insect nets, and polypropylene strapping tape after flat-die conversion. S1003G is not suitable for fine-denier fiber below 0.3 mm die diameter because melt draw resonance appears at take-up speeds above 150 m/min, producing periodic diameter variation. The operational boundary for outdoor use is set by the UV package rather than the base resin: surfaces with active HALS concentration below 0.06 wt% develop surface cracking after 300–400 h of accelerated weathering under ASTM G154-23 cycle 1.

    To maintain sheet gauge uniformity with a 3.0 MFR homopolymer, sheet extrusion of S1003G is operated at lower melt temperatures than BOPP cast film: 210–240 °C at the T-die, with a polished three-roll stack set at 60–80 °C. Sheet thickness for thermoforming is controlled to 0.2–2.0 mm. Because homopolymer PP exhibits a narrow melting range, the infrared thermoforming oven brings sheet surface temperature to 155–170 °C; below 150 °C the sheet stress-whitens at the draw corners, and above 175 °C sag exceeds 10 mm across a 500 mm span, producing nonuniform wall thickness in the formed part. Plug-assisted vacuum forming is required for draw ratios deeper than 1:1; cavity mold temperature is kept at 20–50 °C to avoid post-mold shrinkage exceeding 1.5 % under ASTM D955-21.

    Formulation is limited to 98.0–99.5 wt% S1003G, 0.1–0.5 wt% nucleating agent masterbatch, and 0.5–2.0 wt% white pigment masterbatch for dairy and bakery containers. For clear thermoformed lids, a clarified random copolymer is used in place of S1003G because homopolymer haze prevents the required transparency; S1003G is therefore restricted to pigmented or opaque trays. Direct food-contact sheet must comply with FDA 21 CFR 177.1520 and EU Regulation (EU) No 10/2011; migration testing for the formed article uses food simulants assigned under Annex III, with total migration below 10 mg/dm². Frozen food applications are outside the operational envelope of unmodified S1003G: Charpy notched impact under ISO 179-1/1eA at -20 °C falls below 1.5 kJ/m², and cracking occurs in drop tests from 0.5 m when the tray wall is less than 0.4 mm.

    Terminal products are opaque yogurt cups, dairy-portion packs converted by inline roll-fed thermoforming, bakery trays, disposable plates, produce punnets, and blister packaging for non-food hardware. Sheet extrusion lines built for this grade typically run at 80–120 kg/h on a 75 mm single-screw extruder with L/D 30:1; the specific output is governed by the lower melt temperature and the high melt viscosity of S1003G.

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    Certification & Compliance
    More Introduction

    Polypropylene Homopolymer PP S1003G is a general-purpose isotactic homopolymer resin with a nominal melt mass-flow rate of 3.0 g/10 min when measured at 230 °C under a 2.16 kg piston load in accordance with ISO 1133-1:2022 or ASTM D1238-13. Density values for this grade class are commonly reported from 0.900 g/cm³ to 0.910 g/cm³ under ISO 1183-1:2019 or ASTM D1505-18. The material is differentiated from random copolymers by the absence of ethylene in the propylene sequence, which produces a higher crystalline fraction, higher flexural modulus, lower notched impact toughness, and reduced low-temperature ductility. Converter use is concentrated in general-purpose injection moulding, extrusion of straps, tapes, monofilaments, and sheet, as well as some thermoforming operations where a controlled balance of stiffness and melt strength is required. Manufacturer-specific mill certificates govern final release limits; the values shown below represent the grade class and may vary with additive package and catalyst system.

    PropertyTest standardTypical rangeUnit
    Melt mass-flow rate, 230 °C/2.16 kgISO 1133-1:2022 / ASTM D1238-132.7–3.3g/10 min
    DensityISO 1183-1:2019 / ASTM D1505-180.900–0.910g/cm³
    Tensile stress at yieldISO 527-2:2012 / ASTM D638-1434–38MPa
    Tensile elongation at yieldISO 527-2:2012 / ASTM D638-148–12%
    Flexural modulusISO 178:2019 / ASTM D790-171,400–1,600MPa
    Notched Charpy impact at 23 °CISO 179-1:20202.5–4.0kJ/m²
    Notched Izod impact at 23 °CASTM D256-2325–40J/m
    Vicat softening temperature, A50ISO 306:2022150–156°C
    Heat deflection temperature, 0.45 MPaISO 75-2:201395–105°C
    Rockwell hardness, R scaleASTM D785-2390–100—

    Individual lot certificates from the producing site control grade release and may contain narrower acceptance limits than the general ranges listed above. Values are not to be used as guaranteed specifications without producer confirmation.

    What Distinguishes S1003G from Random and Impact Copolymer Grades?

    Homopolymer PP S1003G contains little or no ethylene comonomer in the propylene sequence. Random copolymers incorporate approximately 1–4 wt% ethylene, which disrupts crystallinity and lowers the melting peak by 5–15 °C relative to homopolymer PP. Impact copolymers introduce a dispersed ethylene-propylene rubber phase within a polypropylene matrix, producing a distinct morphological mismatch between the homopolymer S1003G and heterophasic grades. The structural difference is most visible in stiffness, impact behaviour, and optical appearance.

    AttributeHomopolymer PP S1003GRandom copolymer PPImpact copolymer PP
    Ethylene content<0.5 wt% typical1–4 wt%5–15 wt% total rubber phase
    Flexural modulus1,400–1,600 MPa900–1,200 MPa1,000–1,400 MPa
    Notched Charpy impact at 23 °C2.5–4.0 kJ/m²5–15 kJ/m²10–30 kJ/m²
    Notched Charpy impact at -20 °C1.0–2.0 kJ/m²2–5 kJ/m²5–20 kJ/m²
    Optical appearance in thin wallTranslucent to opaqueTransparent to translucentOpaque
    Typical application focusGeneral injection moulding, tapes, monofilaments, sheetClear containers, film, medical packagingLow-temperature packaging, automotive interior and exterior parts

    The higher isotacticity of S1003G-class homopolymer PP raises the crystalline melt peak to approximately 160–165 °C under ISO 11357-3:2018. Random copolymers with ethylene insertion exhibit broadened melting shoulders and lower peak temperatures, which supports heat-sealing behaviour but reduces heat deflection capability. Impact copolymers retain a homopolymer matrix melting point but lose stiffness because the rubber phase acts as a stress concentrator under flexural loading. For converters requiring sharp dimensional stability and low creep under load, S1003G is preferred over random and impact copolymers within its impact limitation.

    Injection-Moulding Parameter Window and Shrinkage Anisotropy

    Processing of S1003G on production-scale injection-moulding machines is generally performed with barrel set temperatures of 220–250 °C and a nozzle temperature near the upper end of that range to reduce orientation-induced stress. Screw configurations with an L/D of 20:1 to 25:1 and compression ratio of 2.5:1 to 3.0:1 are standard for general-purpose PP. Injection pressure on hydraulic machines is commonly 70–120 MPa at the screw face, depending on gate size, flow length, and wall thickness. Thin-wall parts below 1.5 mm may require injection velocities of 100–200 mm/s and fill times under 1 s to prevent premature skin freezing. Packing pressure is commonly held at 60–80% of peak injection pressure until gate freeze; premature packing release produces sink marks in thicker sections and increases post-mould shrinkage.

    Mould temperature is maintained between 20 °C and 60 °C. Lower mould temperatures reduce cycle time but freeze the surface skin early, increasing flow-linked surface defects and residual stress. Higher mould temperatures reduce orientation stress but extend cycle time and can increase post-mould crystallisation. Dimensional inspection is typically conducted after 48 h at 23 °C under ISO 291:2021, because homopolymer PP continues crystallising after demoulding. Shrinkage measured on 2 mm plaques according to ISO 294-4:2018 commonly ranges from 1.1–1.4% parallel to flow and 1.3–1.6% perpendicular to flow. This anisotropy produces warpage in large rectangular parts when gating is not centrally placed or when cooling channels fail to maintain a uniform mould surface temperature.

    The flow length of S1003G is lower than that of high-flow homopolymer grades with MFR values of 10–35 g/10 min. For multi-cavity tools with long flow paths, cavity pressure requirements increase sharply as wall thickness falls below 1.2 mm. Weld lines in unreinforced homopolymer PP do not recover full base-material strength, so gates should locate weld lines away from load-bearing regions or specified impact surfaces. Published data for the interaction of specific tool coatings with S1003G-class flow fronts is limited.

    When Draw Ratio Exceeds 9:1 in Tape and Monofilament Lines

    In tape and monofilament extrusion, the nominal 3.0 g/10 min MFR provides sufficient melt strength for monoaxial orientation but lower melt strength than blow-moulding grades with MFR below 1.0 g/10 min. A single-screw extruder with an 30:1 L/D barrier screw and melt filtration through 80–120 mesh breaker plates is common. The extrudate is quenched in water at 25–40 °C before entering a hot-air drawing oven at 110–140 °C. The quench bath temperature controls spherulite diameter: bath temperatures below 25 °C produce fine spherulites and improve draw uniformity, while temperatures above 40 °C can produce larger crystalline structures that reduce the attainable draw ratio and promote draw resonance.

    The process window narrows when draw ratio exceeds 9:1. At high draw ratios, line breaks increase and denier variability becomes unacceptable in continuous tape lines. Below 6:1, tensile tenacity may not reach woven-sack specifications. Draw ratio is therefore maintained between 6:1 and 9:1 for S1003G. Drawing at oven temperatures below 110 °C increases draw stress and initiates edge fibrillation; temperatures above 140 °C can cause surface stickiness and sag between rollers. After drawing, annealing at 100–120 °C for 1–2 s reduces residual shrinkage in the finished tape. The final tape strength is sensitive to quench uniformity and draw-oven temperature distribution; converter lines with air-temperature variation above ±5 °C across the web may produce measurable denier shift in S1003G tapes.

    Research on polypropylene orientation indicates that monoaxially drawn homopolymer PP can reach tensile strengths several times higher than the unoriented extrusion yield strength. However, published data for this specific S1003G configuration is limited, and converter-produced tape property ranges depend heavily on line speed, draw gap, and die gap. Die gaps of 0.8–1.2 mm are typical for tape lines, with a die-to-water-bath distance kept short to limit melt sag and diameter variability.

    Pre-drying is not mandatory for S1003G processed in a controlled indoor environment below 60% relative humidity. If pellets have been stored in unheated warehouses or if wet regrind is introduced, surface moisture can produce splay marks on injection-moulded surfaces and bubble defects in tape quench baths. Desiccant drying at 80 °C for 2–4 h is used to bring residual moisture below 0.05 wt% before processing. Food-contact applications are reviewed under FDA 21 CFR 177.1520 for olefin polymers and under EU Regulation (EU) No 10/2011 where the finished article is intended for food contact; compliance depends on the additive package, processing conditions, and converter-specific migration testing. REACH compliance should be confirmed through the producer’s safety data sheet and SVHC declaration.

    Thermo-Oxidative Degradation and Chemical Resistance Boundaries Are Stabilizer-Dependent

    The continuous use temperature in air for stabilised homopolymer PP of this class is commonly specified from 90 °C to 110 °C; the actual relative thermal index should be verified under the producer’s UL 746B listing because different additive packages shift this value. S1003G is not recommended for continuous contact with strong oxidising acids, aromatic solvents, or chlorinated hydrocarbons at elevated temperature. Chlorine-containing potable water at high pressure and temperature can accelerate surface cracking and is outside the typical use envelope for unstabilised or inadequately stabilised homopolymer PP.

    Copper and copper-alloy contact above 100 °C should be avoided because transition-metal catalysis promotes thermo-oxidative chain scission. For outdoor use, a UV-stabilised version should be selected; unstabilised homopolymer PP degrades rapidly under ASTM D4329 UV-A fluorescent exposure and should not be used for long-term outdoor weatherable articles. The mechanical property floor of S1003G at sub-zero temperatures is governed by the glass transition of the propylene backbone and by the local crystalline morphology; impact-limited applications below -20 °C require a heterophasic impact copolymer or a compounded toughening approach rather than the homopolymer grade.