| HS Code | 231335 |
| Product | MOSTEN PP Homopolymer XH 601 |
| Polymer Type | Polypropylene Homopolymer |
| Melt Flow Index 230 C 2 16 Kg | 1200 g/10 min |
| Density | 0.905 g/cm³ |
| Tensile Strength At Yield | 30 MPa |
| Elongation At Yield | 8% |
| Flexural Modulus | 1400 MPa |
| Izod Impact Strength 23 C Notched | 1.6 kJ/m² |
| Vicat Softening Temperature A50 | 150 °C |
| Heat Deflection Temperature 0 45 Mpa | 95 °C |
| Melting Temperature | 165 °C |
| Rockwell Hardness R Scale | 85 |
As an accredited MOSTEN PP Homopolymer XH 601 factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | MOSTEN PP Homopolymer XH 601 is supplied in 25 kg woven polypropylene bags, heat-sealed, palletized and shrink-wrapped for protection. |
| Container Loading (20′ FCL) | 20′ FCL: MOSTEN PP Homopolymer XH 601 packed in 25 kg bags, palletized and secured for safe transport. |
| Shipping | MOSTEN PP Homopolymer XH 601 is a non-hazardous polypropylene resin. Ship in clean, dry containers or bags, protected from moisture, direct sunlight, and heavy contamination. Avoid high temperatures and impact damage. Store upright, keep sealed, and transport in ventilated vehicles with proper load securing. |
| Storage | Store MOSTEN PP Homopolymer XH 601 in a dry, clean, well-ventilated area, away from direct sunlight, heat, and ignition sources. Keep containers tightly sealed to prevent moisture pickup and contamination. Avoid exposure to excessive humidity and dust. No special storage requirements beyond standard polymer handling; protect from mechanical damage and store at ambient temperature. |
| Shelf Life | Store in a cool, dry area away from UV light. Shelf life is typically 12 months from delivery. |
On biaxially oriented polypropylene tenter lines running a three-layer A/B/A structure with MOSTEN PP Homopolymer XH 601 in the core layer, the homopolymer core normally constitutes 70–85 wt% of the total melt stream because the core must provide the draw plateau, tensile modulus, and thickness uniformity required for orientation while the coextruded skin layers manage heat-seal initiation and slip. The compliance anchor for finished BOPP food-contact film is EU No 10/2011, Annex I Table 2, with overall migration ≤ 10 mg/dm², and FDA 21 CFR 177.1520(c), which covers olefin polymers for food-contact use. The core layer is run at 100 wt% XH 601 on a dry-resin basis, while a combined slip/antiblock masterbatch is dosed into the skin layers at 0.10–0.30 wt% antiblock and 0.05–0.20 wt% slip additive to control coefficient of friction and prevent film blocking. Downstream conversion uses a flat die at 240–250 °C, a chill roll at 30–40 °C to quench the cast sheet, machine-direction orientation at 120–135 °C with a draw ratio of 4.5:1–5.5:1, transverse orientation in a tenter oven at 155–165 °C with a draw ratio of 7:1–9:1, and corona treatment to 38–42 mN/m surface energy. Finished goods include printed flexible packaging film, adhesive tape base film, overwrap, and monolayer or coextruded capacitor film when surface-treated. Field observations on BOPP lines show die lip oligomer plate-out after 6–12 h of continuous operation, and this deposit produces transverse gauge bands unless the die lips are cleaned and the vacuum box is adjusted to stabilize the film at the chill roll.
Process stability limits for the homopolymer core are defined by the tenter chain temperature distribution: if the transverse orientation zone falls below 150 °C, the film develops uneven thickness; above 170 °C, the film can exhibit heat-set shrinkage below the 3–5% typical for BOPP measured by ASTM D1204-14. Moisture is normally not a process variable for homopolymer PP, but storage at relative humidity above 60% can introduce surface moisture that creates bubbles in cast quenching; a pre-drying step at 80 °C for 2–4 h is applied when visible surface moisture is present. Avoid blending free-flowing lubricant masterbatches above 0.50 wt% into the core layer because additive migration to the coextrusion interface can reduce interlayer adhesion and cause delamination under heat-seal testing.
Slit tape lines converting XH 601 into woven sack fabric and flexible intermediate bulk containers use water-quenched film as the precursor because controlled supercooling preserves a low crystalline fraction that can be drawn to high tenacity. The governing compliance for FIBC is ISO 21898:2018, which specifies design, construction, and safe working load requirements for flexible intermediate bulk containers, and for food-contact woven sacks the finished fabric must meet EU No 10/2011 or FDA 21 CFR 177.1520 depending on destination. The formulation addition ratio for outdoor or export woven sacks is 100 wt% XH 601 plus 0.5–2.0 wt% UV masterbatch containing hindered amine light stabilizers and a 0.02–0.08 wt% processing aid to reduce die lip deposition; calcium carbonate filler is limited to 0–1.0 wt% for non-food woven sacks because higher loading reduces tape stretchability and increases filament breaks. The production line uses a single-screw extruder with an L/D of 30:1, a flat film die with a gap of 0.8–1.2 mm, a water bath at 25–35 °C, slitting blades spaced 2.5–6.0 mm, a hot-air stretching oven at 130–160 °C, and a draw ratio of 1:6–1:8 before annealing. Finished goods include FIBC side panels and baffles, woven polypropylene sacks, agricultural twine, and woven geotextile fabrics. On production-scale tape lines, the main failure mode observed is melt filtration bypass: a gel particle entering the die lip produces a thin spot that develops into a fibrillated filament break under the 1:7 draw, so backup screen packs at 40/60/80 mesh are commonly used to limit gel carryover.
| Application segment | Standard or regulation | Clause / method designation | Compliance parameter |
|---|---|---|---|
| BOPP packaging film | EU No 10/2011; FDA 21 CFR 177.1520(c); ASTM D1204-14 | Annex I Table 2; paragraph (c); heat shrinkage | Overall migration ≤ 10 mg/dm²; shrinkage 3–5% |
| Woven FIBC and sacks | ISO 21898:2018; EU No 10/2011; FDA 21 CFR 177.1520 | FIBC design and SWL marking; migration | Safe working load marking; food-contact migration limits |
| Thermoformed containers | EU No 10/2011; FDA 21 CFR 177.1520(c); ISO 179-1 | Annex I Table 2; paragraph (c); Charpy impact | Overall migration ≤ 10 mg/dm²; low-temperature impact resistance |
| Spunbond nonwovens | ISO 9092:2019; ISO 9073-1:2022; EDANA NWSP 070.5 | Definition; mass per unit area; tensile | Basis-weight uniformity; tensile strength and elongation |
| Monofilament ropes and twine | ISO 1346:2012; ISO 2307:2019 | Polypropylene monofilament rope; rope testing | Breaking load; linear density |
| Cast film lamination webs | EU No 10/2011; FDA 21 CFR 177.1520(c); ASTM D882-18; ISO 527-3:2018 | Annex I Table 2; paragraph (c); film tensile | Migration limits; tensile elongation |
Rigid thin-wall thermoforming of homopolymer PP sheet requires a narrow sheet surface temperature corridor because homopolymer PP has a sharp melt-crystallization transition and a low melt strength plateau. In this application the compliance anchor is EU No 10/2011 for plastic materials intended to contact food, with overall migration limits referenced in Annex I Table 2, and FDA 21 CFR 177.1520(c) for olefin polymer containers; for material lot release when impact failure is a known field complaint, ISO 179-1 Charpy impact testing is applied. The formulation is 100 wt% XH 601, with a nucleating agent masterbatch at 0.10–0.30 wt% to increase crystallization temperature and reduce cycle time, titanium dioxide white masterbatch at 1.0–3.0 wt% for opacity in dairy packaging, and antistatic masterbatch at 0.2–0.5 wt% for demolding and downstream filling. The sheet extrusion step processes the grade at 230–250 °C melt temperature through a 0.8–1.5 mm die gap onto a polishing stack held at 70–90 °C, followed by inline or roll-fed thermoforming at a sheet surface temperature of 150–170 °C, plug-assisted forming with a plug temperature of 70–95 °C, and mold temperature of 20–40 °C. Finished product types are thin-wall dairy cups, food trays, deli containers, and non-food blister trays. Production field data from roll-fed lines shows edge sag becomes measurable when the sheet edge exceeds 170 °C for more than 3 s, which shifts part wall thickness distribution by more than 0.05 mm and increases reject rates; zonal infrared heating is therefore adjusted to hold the center-to-edge temperature delta below 5 °C.
The operating boundary for XH 601 in refrigerated or frozen food trays is the low-temperature impact regime: unnotched Charpy impact measured by ISO 179-1 declines as service temperature drops below 0 °C, so dairy trays intended for -20 °C storage require an impact-modified skin or blended resin. Avoid dosing nucleating masterbatch above 0.30 wt% because excessive crystallization rate can create brittle weld lines at the plug contact point.
A spunbond beam processing XH 601 requires the melt filter differential pressure to be recorded against screw speed and throughput because gels, unmelts, and high-viscosity domains alter filament diameter distribution and web basis-weight uniformity. The nonwoven compliance framework for hygiene and medical uses includes ISO 9092:2019 for definition and classification of nonwovens, ISO 9073-1:2022 for mass per unit area, EDANA NWSP 070.5 for tensile strength and elongation, and EU No 10/2011 or FDA 21 CFR 177.1520 for food-contact or body-contact layers. The formulation is 100 wt% XH 601 with a melt-stabilizer package at 0.3–0.8 wt% to suppress oxidative degradation during high-temperature spinning, titanium dioxide masterbatch at 0.5–1.2 wt% for opacity in hygiene top sheets, and optionally a topical hydrophilic finish at 0.1–0.5 wt% applied downstream of web bonding. The production process uses a Reicofil-style extruder and metering pump at a melt temperature of 235–250 °C, a spinneret hole diameter of 0.3–0.6 mm, quench air at 10–20 °C for filament cooling, high-velocity air drawing at pressures between 0.1–0.4 bar, web formation on a moving belt, and thermal bonding through an embossed calender at 135–150 °C with a nip pressure of 40–80 N/mm. Finished product types include hygiene top sheets, medical barrier gowns, face mask layers, and industrial sorbent media. In production-scale trials, a filter differential pressure exceeding 80–100 bar indicates screen pack blockage and precedes filament breaks by 30–60 min, so screen packs at 60/80/100 mesh are replaced before pressure drop reaches the upper bound to maintain web tensile uniformity measured by ISO 9073-1:2022.
For monofilament extrusion lines drawing homopolymer PP into twine and rope yarns, the quench water temperature and first-stage draw ratio control the development of a fibrillar core structure that determines tenacity and knot strength. The compliance instruments for finished polypropylene twine and rope are ISO 1346:2012 for polypropylene split-film and monofilament ropes and ISO 2307:2019 for rope testing. Formulation uses 100 wt% XH 601, a UV masterbatch at 0.5–2.0 wt% for outdoor service, and a processing aid at 0.02–0.10 wt% to reduce die face coating. The line extrudes the melt at 230–250 °C through a die hole of 0.8–1.5 mm, quenches the filament in a water bath at 25–35 °C, then draws it in a first-stage oven at 100–120 °C at a ratio of 1:5–1:7, draws again at 140–155 °C at a ratio of 1.1:1–1.3:1, and relaxes the filament 3–6% on a heated godet. Terminal products are baler twine, rope yarn, netting, and carpet backing yarn. Field data from monofilament lines show necking instability occurs when the first-stage draw ratio exceeds 1:7 at line speeds above 250 m/min, producing a periodic diameter oscillation that is detected by in-line laser gauge at ±0.02 mm; the corrective action is to reduce first-stage draw ratio or raise oven temperature by 5–10 °C.
Cast film lines running XH 601 as the stiff core or backing layer in lamination structures rely on chill roll contact uniformity to prevent transverse gauge bands, blocking, and haze. The regulatory reference for food-contact lamination film is EU No 10/2011 with Annex I Table 2 migration limits and FDA 21 CFR 177.1520(c), while mechanical properties are compared under ASTM D882-18 for thin plastic sheeting and ISO 527-3:2018 for film tensile. The formulation for a monolayer or core layer is 100 wt% XH 601, with slip/antiblock masterbatch at 0.05–0.25 wt% depending on roll release and downstream corona treatment, and optional processing aid at 0.02–0.08 wt% to reduce die lip deposit. The production process uses a flat die at 230–250 °C, a chill roll at 15–30 °C with an air knife to pin the melt curtain, and line speeds from 100–300 m/min for films of 20–80 µm. Finished goods include lamination base films for flexible packaging, surface protection film backing, document lamination, and pressure-sensitive label backing. On high-speed cast film lines, chill roll surface defects or inadequate air knife pressure create gauge bands that are detected by online thickness mapping at ±1.5%; if the chill roll temperature is raised above 30 °C, surface blocking can occur on the winder because homopolymer PP lacks the low-crystallinity skin of random copolymers. Haze is monitored by ASTM D1003-21, and for niche lamination structures below 15 µm, published data for this specific configuration is limited, so start-up trials are required to confirm the line settings.
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MOSTEN PP Homopolymer XH 601 is a polypropylene homopolymer marketed within the Mosten portfolio of ORLEN Unipetrol. The grade belongs to the iso-tactic propylene homopolymer family classified under ISO 1873-2 and is distinguished from random copolymer grades by the absence of deliberately copolymerised ethylene. The homopolymeric architecture raises the isotactic helical content and produces an α-phase-dominated crystalline structure with a melting endotherm typically measured between 160 °C and 165 °C under ISO 11357-3. Density for unfilled PP-H grades of this class falls in the 0.900–0.910 g/cm³ range under ISO 1183-1. These characteristics result in higher short-term heat resistance and higher tensile modulus than equivalent melt-flow random copolymers, while the absence of an ethylene-propylene rubber phase reduces low-temperature impact strength. The product therefore occupies a specification space between general-purpose injection moulding grades and impact-modified heterophasic copolymers. Technical evaluation of MOSTEN PP Homopolymer XH 601 should use the producer’s current certificate of analysis, because additive formulation and lot-to-lot rheology can shift within the published specification band. The grade’s primary differentiating feature is stiffness retention through the upper end of the polypropylene working temperature window; this is exploited in rigid packaging, closures, technical mouldings, and high-orientation tape and fibre processes.
Melt mass-flow rate is the primary specification variable for classifying the grade within ISO 1873-2. The value is measured at 230 °C with a nominal load of 2.16 kg using ISO 1133-1:2022. Homopolymer extrusion and injection grades in the Mosten family are typically specified with an MFR between 2 g/10 min and 12 g/10 min; the exact figure for XH 601 is to be confirmed on the batch certificate. The MFR controls whether the melt can be processed on a standard three-zone injection screw without excessive injection pressure. For single-screw extrusion, medium-MFR PP-H is usually processed with a barrel temperature profile from 220 °C to 250 °C. The die temperature is generally kept within 10 °C of the metering-zone setpoint to avoid die-lip freeze-off and melt-pressure oscillation. If the melt temperature exceeds 260 °C, thermo-oxidative chain scission can reduce molecular weight and melt strength; the stabilizer package is designed for short residence excursions, not continuous operation above the specified limit. In grooved-barrel extruders, feed-zone cooling water at 20–40 °C is used to prevent premature pellet melting in the feed bushing. The specific energy consumption in the plastication section of a 33:1 L/D single-screw extruder is influenced by back pressure; for PP-H tape and fibre operations, die pressure values between 80 bar and 200 bar are serviceable depending on melt filtration and die-land geometry.
On injection moulding lines, the feed throat should be monitored for obstruction because chilled granules can bridge when the hopper is loaded from ambient storage below 10 °C. The material is best processed with a general-purpose screw having an effective screw length of 18:1 to 22:1 L/D, a compression ratio of 2.0:1 to 2.5:1, and a non-return valve with hardened surfaces. Clamp force should be calculated from cavity pressure projections; for unfilled PP-H formulations, a specific clamp force of 2.5 to 5.0 kN/cm² of projected area is a common starting range for technical parts. Injection velocity should be profiled to prevent jetting in thick-to-thin transitions; a fast fill of the gate and runner followed by a slower packing transition reduces gate blush. Holding pressure is maintained until the gate freezes. Packing pressure between 400 bar and 800 bar is typical for medium-flow PP-H, but cavity pressure transducers should be used to avoid overpacking ribs and bosses. Mould temperature should be held between 20 °C and 40 °C to balance surface gloss and crystallinity; a higher mould temperature of 50–60 °C raises crystallinity and tensile modulus but extends cycle time and can increase warpage in asymmetric parts. Ejection can begin when the core temperature falls below the heat-deflection temperature; for PP-H the HDT under 0.45 MPa is approximately 90–110 °C, but part design should not rely solely on this value because HDT is not a creep limit.
The defining difference is comonomer architecture. Random copolymer grades incorporate ethylene or butene into the polymer backbone, reducing crystallite size, melting point, and tensile modulus. Heterophasic copolymers disperse a rubbery ethylene-propylene phase in a polypropylene matrix, producing a step-change in impact strength at the expense of stiffness and heat resistance. XH 601, as a homopolymer, has the highest crystallinity of the three classes; this raises tensile modulus and Vicat softening temperature but lowers notched Charpy values at sub-zero temperatures. Table 1 provides class-level ranges for initial material selection. The comparison is not a product-specific datasheet; designers should request exact lot data for XH 601 before locking tooling or regulatory submissions.
| Property | Test method | Unfilled PP-H class | PP random copolymer | PP heterophasic copolymer |
|---|---|---|---|---|
| Melting peak temperature | ISO 11357-3 | 160–165 °C | 130–148 °C | 160–165 °C |
| Tensile modulus | ISO 527-2 | 1,300–1,600 MPa | 800–1,200 MPa | 900–1,300 MPa |
| Notched Charpy impact at 23 °C | ISO 179-1/1eA | 2–5 kJ/m² | 5–15 kJ/m² | 15–50 kJ/m² |
| Vicat softening temperature B50 | ISO 306 | 150–158 °C | 120–140 °C | 120–150 °C |
| Density | ISO 1183-1 | 0.900–0.910 g/cm³ | 0.890–0.900 g/cm³ | 0.890–0.900 g/cm³ |
For cap and closure applications, the lower creep of homopolymer PP under continuous load is relevant. Creep modulus measured according to ISO 899-2 at 23 °C and 1,000 h is typically higher for PP-H than for impact copolymers, making the homopolymer suitable for threaded closures that must maintain preload during distribution and warehouse storage. However, the trade-off is reduced ductility in cold environments; published data for XH 601 impact strength at −20 °C is limited, so freezer applications require end-product testing. The homopolymer also has lower moisture absorption than polyamide and requires no pre-drying unless bulk storage condensation has occurred; if the pellet surface is wet, a desiccant dryer at 70–80 °C for 2–4 h with a dew point below −20 °C is sufficient to remove surface moisture.
Compliance verification for this grade must be performed on the finished packaging or moulded article. The supplier’s food-contact declaration for PP-H grades typically references EU Regulation 10/2011 and FDA 21 CFR 177.1520, but the declaration is valid only for the specific grade and is subject to overall migration and specific migration limits. For general food-contact exposure, the overall migration limit under EU Regulation 10/2011 is 10 mg/dm² for plastic materials, and certain specialized applications may require lower or higher migration limits depending on the simulant and contact ratio. The US 21 CFR 177.1520(c) clearance is an olefin polymer clearance; end-product extraction tests follow the procedures in 21 CFR 177.1520(d) and are not automatically satisfied by resin certification alone. Under REACH (EC) 1907/2006, a polymer as such is exempt from registration, but intentionally added monomers above 0.1 wt% are managed through monomer registration; the safety data sheet should state the stabilizer package. RoHS Directive 2011/65/EU restriction applies only to electrical and electronic equipment and sets maximum concentration values of 0.1 wt% for lead, mercury, hexavalent chromium, polybrominated biphenyls, and polybrominated diphenyl ethers, and 0.01 wt% for cadmium in homogeneous materials. Finished-article converters should verify these limits by XRF screening or wet-chemical digestion because recycled process scrap can introduce trace metals beyond the base resin’s typical profile.
| Standard / regulation | Measurement or clause | Typical requirement or limit |
|---|---|---|
| EU Regulation 10/2011 | Overall migration, food simulant immersion | 10 mg/dm² general limit |
| FDA 21 CFR 177.1520 | Olefin polymer clearance | End-product extraction limits per 177.1520(c) and (d) |
| REACH (EC) 1907/2006 | SVHC screening | Supplier SDS and SVHC list declaration |
| RoHS Directive 2011/65/EU | Homogeneous material XRF or wet chemistry | Pb, Hg, Cr(VI), PBB, PBDE max 0.1 wt%; Cd max 0.01 wt% |
Thermo-oxidative stability is governed by the additive package and processing history. The resin should not be held at melt temperature longer than necessary because sequential processing reduces the antioxidant reservoir and lowers the oxidative induction time. OIT is measured by differential scanning calorimetry under oxygen at an isothermal temperature, commonly 200 °C according to ISO 11357-6. A typical stabilizer-loaded PP-H compound may show an OIT of 10–30 min at 200 °C, but unfilled XH 601 lot data must be obtained from the producer. Repeated extrusions in a corotating twin-screw extruder with an L/D of 40:1 and a screw speed above 300 min⁻¹ can reduce molecular weight by chain scission and lower melt viscosity; viscosity retention at high shear should be verified by parallel-plate rheometry under nitrogen. For applications demanding long-term thermal aging above 100 °C, the stabilizer package may require augmentation with a long-term heat stabilizer or a phenolic/phosphite blend; any modification must be evaluated for food-contact compliance and plate-out characteristics. Peroxide-based controlled-rheology additives should be avoided where melt strength is critical, because chain scission increases the melt flow rate and reduces the high-molecular-weight tail that supports extensional flow in tape stretching and cast-film drawing.
For single-layer cast film and tape extrusion, the die gap and draw ratio should be matched to the melt strength of the homopolymer. On a cast-film line with a die gap of 0.5–1.0 mm and no air-gap correction, homopolymer PP may draw at ratios below 10:1 before edge instability, depending on melt temperature and die geometry. A vacuum box can improve contact with the chill roll; the chill-roll temperature is maintained between 15 °C and 30 °C to control crystallinity and haze. In oriented tape lines, a water-bath temperature of 30–40 °C is used to freeze the primary sheet before stretching; the stretch ratio is normally between 7:1 and 9:1 for PP-H tape, with a hot-air or hot-roll temperature of 110–130 °C. Higher stretching ratios can be achieved but require higher molecular weight or lower MFR; operators should avoid increasing the draw ratio beyond the point where the web shows periodic thickness bands, because this indicates necking instability. For injection moulded caps, gasket moulding or liner insertion must be validated because homopolymer PP has a coefficient of linear thermal expansion in the range 100–150 ×10⁻⁶ K⁻¹ under ISO 11359-2; changes in part dimensions between 20 °C and 80 °C can exceed the tolerance for tamper-evident band articulation if the mould is not shrink-compensated. The final mould trial should include dimensional checks after 48 h because post-mould crystallization continues and can reduce diameter by up to 0.5 % depending on wall thickness and nucleating agent content.