| HS Code | 248615 |
| Product Name | MARLEX PP HD168MO |
| Material Type | Polypropylene Homopolymer |
| Density | 0.902 g/cm³ |
| Melt Flow Rate | 20 g/10 min (230°C/2.16 kg) |
| Tensile Strength At Yield | 34.5 MPa |
| Elongation At Yield | 10% |
| Flexural Modulus | 1700 MPa |
| Izod Impact Notched 23c | 27 J/m |
| Rockwell Hardness | R-100 |
| Heat Deflection Temperature 0 45mpa | 110°C |
| Heat Deflection Temperature 1 82mpa | 54°C |
| Vicat Softening Temperature | 154°C |
As an accredited MARLEX PP HD168MO factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | MARLEX PP HD168MO is packaged in 25 kg polyethylene-lined paper bags, ensuring product purity and safe handling. |
| Container Loading (20′ FCL) | 20′ FCL container loading for MARLEX PP HD168MO: palletized 25 kg bags, about 25 tons per container, secured for safe transit. |
| Shipping | MARLEX PP HD168MO is a polypropylene resin supplied as free-flowing pellets. Ship in clean, dry containers or railcars to prevent contamination and moisture absorption. Avoid excessive heat and direct sunlight. Standard non-hazardous shipping procedures apply; keep away from ignition sources during handling and transport. |
| Storage | Store MARLEX PP HD168MO in a cool, dry, well-ventilated area, away from direct sunlight, heat, and ignition sources. Keep containers tightly sealed to prevent moisture and contamination. Avoid dust accumulation and static discharge. Use original packaging and rotate stock to ensure proper shelf life. Handle with clean equipment. |
| Shelf Life | Shelf life is indefinite when stored properly in a sealed container, away from heat, moisture, and direct sunlight. |
Incoming lot rheology checks for Marlex PP HD168MO in a high-output thin-wall molding operation generally include ASTM D1238-23 and ISO 1133-1:2022 at 230 °C/2.16 kg. A representative melt flow rate acceptance band is 14–18 g/10 min. Pellet moisture above 0.10 wt% by Karl Fischer titration requires dehumidified-air drying at 80 °C for 2 h. A 24-cavity hot-runner mold with 0.45 mm nominal wall thickness is operated with melt temperature 230–250 °C, cold-mold temperature 12–25 °C, injection velocity 120–180 mm/s, and holding pressure 55–75 MPa. When melt temperature overshoots 250 °C, oxidative chain scission raises MFR by roughly 1.0–2.5 g/10 min per 10 °C overshoot, appearing first as short-shot hesitation and later as parting-line flash. Finished-container compliance is assessed under FDA 21 CFR 177.1520 for olefin polymers, but raw-pellet certification does not replace finished-article migration testing under FDA 21 CFR 174.5 or EU Regulation No 10/2011, where the overall migration limit is 10 mg/dm². Terminal articles include deli tubs, portion cups, and snap-lid bases.
Closure production on 64-cavity hot-runner tools exposes pellet-to-pellet MFR variation. A shift of 0.8 g/10 min within the accepted range can re-order cavity filling, with the last cavities receiving a lower-viscosity fraction and packing more quickly. Molders typically set melt temperature 215–235 °C, mold temperature 8–15 °C, screw back pressure 6–12 MPa, and holding time 1.5–2.5 s. Gate freeze-off is confirmed by increasing hold time until part mass stabilizes below 0.05 g change, then hold pressure is set 10–15 MPa above the minimum mass plateau. Sink marks at the tamper-evident tether hinge are tied to hold-pressure decay before gate seal. Dimensional checks follow ISO 2859-1 with AQL 0.65 for critical seal diameters. Torque retention is tested after 24 h at 23 °C/50% RH using a calibrated torque analyzer. For food-contact closures, EU Regulation No 10/2011 requires overall migration below 10 mg/dm² and specific migration limits for additives. US submissions cite FDA 21 CFR 177.1520. Terminal products include beverage caps, detergent closures, and trigger-spray overcaps.
| Process parameter | Thin-wall food container | Closure molding | Talc-filled duct compounding |
|---|---|---|---|
| Melt temperature | 230–250 °C | 215–235 °C | 170–230 °C |
| Mold temperature | 12–25 °C | 8–15 °C | not applicable |
| Hold pressure | 55–75 MPa | 55–70 MPa | not applicable |
| Screw speed | 80–120 rpm | 60–100 rpm | 400–600 rpm |
| Receiving acceptance method | ASTM D1238-23 | ISO 1133-1:2022 | ISO 527-2 |
In steam-sterilized laboratory settings, pipette tips and centrifuge tubes made from Marlex PP HD168MO are commonly molded in 16-cavity hot-runner tools with melt temperature 220–245 °C and mold temperature 8–20 °C. The homopolymer is not a direct substitute for polypropylene random copolymer in impact-resistant freezer storage, but it produces rigid thin-wall tips when injection speed is raised to 150–220 mm/s and holding pressure is capped at 50–70 MPa to prevent gate cracking. Steam sterilization at 121 °C for 30 min causes dimensional relaxation after the first cycle. Dimensional change can reach 0.8–1.5% in the flow direction and should be characterized by ISO 294-4 shrinkage plaques. Heat deflection temperature near 85–95 °C at 0.455 MPa per ISO 75-2 means that autoclaving under clamp load is not recommended unless the part has been annealed and re-measured. Neat-resin certification to USP <661.1> and USP <661.2> is not sufficient for final device release. Biocompatibility endpoints must be tested according to ISO 10993-1:2018, with ISO 10993-5:2009 for cytotoxicity and ISO 10993-10:2010 for irritation or sensitization on finished molded parts. Gamma sterilization above 25 kGy may cause yellowing and measurable loss in elongation at break per ASTM D638-14. Published data for this specific grade under repeated steam cycles is limited; end users must run their own validation.
Under-hood HVAC ducts and air cleaner housings use a compound of Marlex PP HD168MO with 20–30 wt% compacted talc. The downstream conversion is a compounding step on a co-rotating twin-screw extruder with L/D 40:1 to 48:1 and a side-feed port for talc. Base resin enters the main throat. Talc is fed downstream to limit plate-like particle breakage and to prevent metal-filler contact in the melting zone. Barrel temperatures are set from 170 °C at the feed throat to 220 °C before the die, with melt temperature held below 235 °C to avoid talc surface degradation and peroxide-catalyzed chain scission. Screw speed is typically 400–600 rpm, and specific mechanical energy input is 0.18–0.25 kWh/kg, depending on talc packing fraction. Vacuum devolatilization at -0.08 MPa is applied two barrel diameters before the die to reduce volatile condensate that would otherwise plate out in the downstream injection molder vent. A 150 µm melt filter removes agglomerates above 150 µm. Flexural modulus is monitored by ISO 178, and tensile modulus by ISO 527-2. At 20 wt% talc, modulus increases relative to neat PP homopolymer, but published data for this specific grade at all talc loadings is limited. The actual modulus gain should be generated with the exact talc particle size distribution and top size. Low-VOC performance for automotive interiors may be assessed by VDA 278:2011, but a separate emission test on the compounded pellet or molded part is required. Terminal parts include HVAC ducts, resonator chambers, and air cleaner housings.
Unfilled Marlex PP HD168MO is used for small-appliance housings, terminal covers, and internal electrical enclosures. Comparative tracking index under IEC 60112 is tested on a 3 mm plaque. Typical polypropylene homopolymer CTI values exceed 600 V. However, the material is not inherently flame retardant and is rated HB under UL 94 unless flame-retardant additives are incorporated. Glow-wire testing per IEC 60695-2-11 at 750 °C is commonly specified for unattended appliance housings. The test records ignition and flame persistence after the glow wire is removed. Molding conditions influence the result because wall sections below 1.0 mm and mold temperatures above 30 °C can induce orientation and reduce effective glow-wire tolerance. Injection parameters are set at melt temperature 220–245 °C, mold temperature 15–30 °C, and injection velocity 60–120 mm/s. Post-molding annealing at 90 °C for 2 h improves dimensional stability in service near 80–90 °C but does not confer flame retardancy. Compliance with IEC 60335-1 must be verified on the finished appliance. Terminal products include internal relay covers, terminal blocks, and small-appliance housings.
For high-gloss storage boxes and cutlery trays produced from Marlex PP HD168MO, polished mold surfaces and cold-runner or hot-runner tools are used. The molding window is melt temperature 220–245 °C and mold temperature 10–30 °C. Mold temperature above 30 °C raises gloss but extends cycle time and increases the risk of sink marks on ribbed bases. Back pressure of 8–14 MPa homogenizes the melt and removes traces of unmelted fines. Warpage in flat lids is controlled by reducing packing pressure after the first 1.0 s of hold and increasing cooling time to 8–12 s. After repeated dishwasher cycling at 65 °C in alkaline detergent, stress whitening occurs at gate locations if packing pressure exceeds 80 MPa. This is a processing failure rather than a resin failure and is diagnosed by polarized light microscopy. Terminal products include storage boxes, drawer organizers, and kitchen drawer inserts. For food-contact housewares sold in the EU, Regulation (EC) No 1935/2004 and EU Regulation No 10/2011 apply. Non-food housewares are evaluated under REACH Annex XVII for restricted substances.
Direct conversion of Marlex PP HD168MO to meltblown nonwovens without a reactive visbreaking step is not practical. Meltblown dies require much lower melt viscosity, typically corresponding to peroxide-modified PP with MFR 800–1800 g/10 min at 230 °C/2.16 kg. The grade at 14–18 g/10 min causes spinneret hole wetting, high die pressure, and unacceptable filament breaks. The correct route is reactive visbreaking in a twin-screw extruder using a di-tert-butyl peroxide masterbatch at 0.05–0.15 wt% peroxide, with barrel temperatures above the peroxide half-life temperature, generally 210–230 °C, and residence time 30–60 s. The effluent is pelletized and then analyzed by ISO 1133-1:2022 because peroxide residue above 5 ppm can cause odor in the nonwoven. This conversion is only permissible when the downstream use permits peroxide-modified resin. Food-contact and medical packaging may reject visbroken grades because the additive package and degradation products must be re-cleared. Published data for this specific grade in meltblown conversion is limited; pilot-line validation is required.
Competitive MARLEX PP HD168MO prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please contact us at +8618136850665 or mail to admin@ascent-chem.com.
We will respond to you as soon as possible.
Tel: +8618136850665
Email: admin@ascent-chem.com
Flexible payment, competitive price, premium service - Inquire now!
Marlex PP HD168MO is a polypropylene homopolymer grade positioned for injection-moulded rigid articles that require high stiffness, moderate heat resistance, and predictable post-mould shrinkage. The grade designation belongs to the Marlex polypropylene product line; available datasheets classify it as a high-crystallinity homopolymer, which separates it from propylene-ethylene random copolymers by a markedly higher flexural modulus and from impact copolymers by the absence of a deliberate rubber phase. Published data for this specific grade are not uniformly available in public literature; therefore, the numerical ranges below are representative of high-crystallinity Marlex PP homopolymers in the same melt-flow classification and should be verified against the current lot certificate.
The grade is supplied as pelletised feedstock with density between 0.900 g/cm³ and 0.910 g/cm³ when measured under ISO 1183-1:2019 or ASTM D792-20. Melt flow rate, determined at 230 °C with a 2.16 kg load under ISO 1133-1:2022, is the primary processing discriminator. For HD168MO-class material, the melt flow rate typically falls between 8 g/10 min and 20 g/10 min; the exact value must be taken from the certificate because a shift of 2 g/10 min can alter shortest fill time and cavity pressure transmission. The product converts by open-loop injection moulding rather than profile extrusion or blow moulding. Typical end-use categories include rigid caps and closures, appliance housings, storage containers, and industrial packaging where side-wall deflection under load must be minimised.
On production-scale hydraulic injection machines with clamp force capacity of 0.5 tonnes/cm² to 0.8 tonnes/cm² of projected area, the barrel should be profiled so that the melt temperature at the nozzle stays between 200 °C and 230 °C. The feed throat is maintained below 60 °C to prevent pellet bridging. If the nozzle falls below 190 °C, short shots occur in walls below 1.5 mm because the crystalline fraction is not fully disengaged and the apparent viscosity remains too high for thin-section filling. If the nozzle remains above 230 °C for more than 5 min, thermal-oxidative chain scission accelerates, producing free radicals that reduce molecular weight and shift melt flow rate upward. This shift can create flash at the parting line and lower notched impact force, even if the visual surface appears unchanged.
Pre-drying is not required when storage relative humidity remains below 60%. When condensation is visible, a desiccant dryer set to 80 °C for 2 h to 3 h is sufficient; drying above 90 °C can cause pellet agglomeration and feed-throat blockage. The screw should have an L/D ratio between 20:1 and 24:1 and a compression ratio between 2.5:1 and 3.5:1. Back pressure is normally set at 0.5 MPa to 1.5 MPa to homogenise melt temperature without excessive shear heating. Injection speed should be profiled: a slow initial advance of 30 mm/s to 60 mm/s at the gate, followed by 100 mm/s to 150 mm/s during cavity filling, reduces jetting and improves weld-line integrity. Hold pressure is set to 40% to 60% of peak injection pressure; hold time is commonly 3 s/mm to 8 s/mm of nominal wall thickness. Lower hold pressure produces sink marks because crystallisation shrinkage of 1.2% to 1.6% in the flow direction must be fed from the gate until seal. Higher hold pressure can increase residual stress and gate stress whitening.
Short-term mechanical response follows the general pattern of a high-crystallinity homopolymer: tensile yield strength is typically 34 MPa to 38 MPa when tested at 50 mm/min under ISO 527-2:2012. Flexural modulus, measured at 2 mm/min under ISO 178:2019, falls between 1.5 GPa and 1.8 GPa. This modulus envelope is materially higher than that of a random copolymer with similar flow, which typically shows 0.9 GPa to 1.2 GPa. Notched Izod impact resistance by ISO 180:2023 is 1.5 kJ/m² to 3.5 kJ/m² at 23 °C and 1.0 kJ/m² to 2.0 kJ/m² at 0 °C. The product therefore cannot blunt cracks effectively and is not selected for sub-zero impact duty; its selection is driven by static rigidity and dimensional stability. Heat deflection temperature at 0.45 MPa under ISO 75-2:2013 generally lies between 95 °C and 110 °C, placing it above common random copolymers that may deflect between 75 °C and 90 °C under the same stress. Rockwell hardness by ISO 2039-2:1987 or ASTM D785-23 is on the 90 to 100 R-scale, contributing to surface scratch resistance but also increasing gate-trim brittleness.
Lot-to-lot melt flow variation of ±1.5 g/10 min can require adjustment of injection speed or hold pressure. On machines without closed-loop melt-pressure control, converters should hold a cushion of 2 mm to 5 mm and monitor screw recovery time. A recovery-time increase of more than 5% from the qualification baseline often indicates higher viscosity, a feed blockage, or a mis-set rear zone. A recovery-time decrease of the same magnitude may indicate chain scission or contamination with a higher-flow resin.
Differential scanning calorimetry under ISO 11357-3:2018 places the main crystalline melting peak between 160 °C and 165 °C, with a recrystallisation exotherm during cooling between 110 °C and 120 °C. The crystalline weight fraction is usually 50% to 60%, and the heat of fusion is typically 145 J/g to 160 J/g. This heat must be removed in the mould, so cooling time scales with wall thickness squared. For a 2 mm wall at a mould surface temperature of 30 °C, cooling times of 8 s to 14 s are common. Raising mould temperature to 50 °C to 60 °C improves gloss and reduces weld-line visibility but increases cycle time and post-mould shrinkage. Lower mould temperatures below 20 °C can freeze the gate too early and increase moulded-in stress.
Mould shrinkage measured on 60 mm × 60 mm × 2 mm plaques under ISO 294-4:2018 is 1.2% to 1.6% in the flow direction and 1.3% to 1.7% in the transverse direction. The difference arises from flow-induced molecular orientation and subsequent oriented crystallisation. Differential shrinkage is the main driver of warpage in flat lids and rectangular containers. Tool design should create a linear flow front and maintain packing pressure until gate seal. Hold pressure below 40% of peak injection pressure often produces underpacked central regions; above 60%, residual stress increases and may produce stress whitening at the gate. The practical melt-temperature window is narrow: below 190 °C, screw recovery torque can rise sharply because pellets are not fully plasticised; above 240 °C, degradation can shift melt flow rate by more than 10% over 30 min residence. Older machines with poor barrel-zone control should operate in a narrower profile of 200 °C to 220 °C to limit lot-to-lot variability.
The grade is not a polyethylene blend. Admixture of high-density polyethylene above 2 wt% can reduce flexural modulus by 10% to 20% and produce iridescent flow lines from phase separation. It should not be dry-blended with amine-based additive masterbatches that can bloom in high-humidity service. Standard phenolic-phosphite stabilisation is typical, but the converter should confirm the stabiliser package with the supplier for heated or long-duration end-use.
For material substitution studies, the following property envelope compares the HD168MO-class homopolymer with a random copolymer and a high-flow polypropylene homopolymer. All values are typical screen ranges and do not replace lot certification.
| Property and test standard | HD168MO class | Random copolymer | High-flow PP homopolymer |
|---|---|---|---|
| Melt flow rate, ISO 1133-1:2022 | 8–20 g/10 min | 5–15 g/10 min | 25–60 g/10 min |
| Flexural modulus, ISO 178:2019 | 1.5–1.8 GPa | 0.9–1.2 GPa | 1.4–1.7 GPa |
| Notched Izod impact, 23 °C, ISO 180:2023 | 1.5–3.5 kJ/m² | 6–12 kJ/m² | 1.2–2.5 kJ/m² |
| Heat deflection temperature, 0.45 MPa, ISO 75-2:2013 | 95–110 °C | 75–90 °C | 90–105 °C |
| Mould shrinkage, flow direction, ISO 294-4:2018 | 1.2–1.6% | 1.0–1.4% | 1.3–1.7% |
Compliance statements must be derived from grade-specific certification, not from generic polypropylene clearances. Polypropylene homopolymers may be cleared for food-contact use under 21 CFR 177.1520 if the finished article meets the applicable extractive limits. Under EU Regulation No 10/2011, overall migration into the specified food simulants must not exceed 10 mg/dm² for most single-use applications; repeated-use articles must also satisfy specific migration limits for the stabiliser package. The HD168MO designation should not be treated as a medical-grade identifier. Unless the supplier has issued an affirmative statement under ISO 10993-1 or a related evaluation, the grade is not appropriate for medical devices or pharmaceutical packaging.
For household chemical exposure, the homopolymer exhibits limited stress-crack resistance to chlorinated solvents and aromatic hydrocarbons. Short-term contact with dilute acids and alkalis at 23 °C is generally acceptable, but oxidative environments such as hot chlorinated water or high-temperature bleach solutions can produce surface crazing. Long-term outdoor exposure requires a stabilised grade or a UV-absorber masterbatch. Unstabilised polypropylene homopolymer can lose more than 50% of tensile elongation after 2000 h to 4000 h of accelerated QUV-A weathering under ISO 4892-3:2024.
The following checklist summarises the regulatory and handling boundaries that should be confirmed with the lot certificate.
| Requirement | Standard or regulation | Typical limit or condition |
|---|---|---|
| US food-contact clearance | 21 CFR 177.1520 | End-use extractive limits apply |
| EU food-contact overall migration | EU 10/2011 | 10 mg/dm² |
| REACH SVHC disclosure | EC 1907/2006 | 0.1 wt% per candidate-list substance |
| RoHS cadmium | 2011/65/EU | 100 ppm maximum |
| RoHS lead/mercury | 2011/65/EU | 1000 ppm maximum each |
On a 120-tonne hydraulic moulding machine with a 40 mm screw and a two-cavity cold-runner tool, comparable Marlex PP homopolymer classes have shown that setting the rear barrel zone to 180 °C reduces screw motor load but increases melt-pressure variation at the transfer point. A flat profile of rear 200 °C, centre 210 °C, front 220 °C, and nozzle 220 °C provides more stable recovery. If the cycle is recovery-limited rather than cooling-limited, back pressure should be raised within the 0.5 MPa to 1.5 MPa range before increasing barrel temperature.
When regrind is introduced into non-critical packaging, the fraction is typically held between 10% and 30%. Regrind must be free of fines because fines accelerate thermal oxidation and create black specks. The grade can be sorted in PP streams by density separation at 0.96 g/cm³ to 1.00 g/cm³ or near-infrared resin identification. Contamination from polycarbonate or PET above 2 wt% can cause delamination and surface defects. In a multi-cavity tool, batch-to-batch melt flow variation should be controlled so that the cushion does not fall below 2 mm; loss of cushion causes pressure loss at the gate and produces sink marks in the thickest section of the article.