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API Megol AM SEBS-Comp. DP2217/60PBT

    • Product Name: API Megol AM SEBS-Comp. DP2217/60PBT
    • Factroy Site: Yinchuan, Ningxia, China
    • Price Inquiry: sales8@ascent-chem.com
    • Manufacturer: Ascent Petrochem Holdings Co., Limited
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    VTB
    Specifications
    HS Code 547075
    Product Name API Megol AM SEBS-Comp. DP2217/60PBT
    Material Type SEBS thermoplastic elastomer compound
    Processing Method injection molding
    Melt Temperature C 180-220
    Mold Temperature C 20-50
    Shrinkage Percent 0.8-1.5
    Color natural or black
    Form pellets
    Adhesion To Pbt yes

    As an accredited API Megol AM SEBS-Comp. DP2217/60PBT factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing API Megol AM SEBS-Comp. DP2217/60PBT is supplied in 25 kg moisture-proof polyethylene-lined bags, palletized and clearly labeled.
    Container Loading (20′ FCL) 20′ FCL container loaded with chemical API Megol AM SEBS-Comp. DP2217/60PBT, securely palletized, stowed, and sealed for transport.
    Shipping API Megol AM SEBS-Comp. DP2217/60PBT is shipped as a non-hazardous thermoplastic elastomer compound; not regulated under DOT/IMDG/IATA. No UN number, hazard class, or packing group is assigned. Keep containers sealed during transport in a cool, dry, ventilated area; avoid dust, heat, and ignition sources; wear standard PPE.
    Storage Store in a cool, dry, well-ventilated area away from direct sunlight, heat sources, ignition, and moisture. Keep original containers tightly closed and palletized to prevent contamination or deformation. Avoid contact with incompatible chemicals and follow local regulations. Maintain stable temperature and humidity, use first-in-first-out stock rotation, and inspect containers regularly for damage.
    Shelf Life For API Megol AM SEBS-Comp. DP2217/60PBT, shelf life is typically 24 months when stored unopened in a cool, dry place away from sunlight.
    Application of API Megol AM SEBS-Comp. DP2217/60PBT

    PBT Substrate Bonding Requires a Bicontinuous Phase Domain

    In two-shot injection molding of PBT-based electrical connector housings with a 60 Shore A SEBS compound, the interfacial zone between the pre-molded polyester substrate and the second-shot elastomer governs long-term assembly integrity. The material designated API Megol AM SEBS-Comp. DP2217/60PBT is formulated with a polybutylene terephthalate modification, typically 10–25 wt% relative to the SEBS matrix in commercially available adhesion-modified grades at this hardness, to generate a dispersed or co-continuous PBT domain structure within the styrene-ethylene-butylene-styrene continuous phase. Published single-grade processing data specific to DP2217 remains limited in open supplier literature; the parameters that follow represent production-validated ranges for SEBS-PBT compounds at 60 Shore A with comparable two-phase morphology. During the second-shot dwell phase—conventionally 15–30 seconds at a holding pressure of 30–50 MPa on a rotary platen two-shot machine with clamping force 120–200 tonnes and an injection unit L/D ratio of 20:1 to 24:1—the PBT domains undergo melt-state interdiffusion across the interface into the substrate PBT crystalline regions, forming a transcrystalline interlayer. Substrate surface temperature at the moment of second-shot injection must exceed the styrene-domain glass transition temperature, maintained between 95°C and 120°C. Failure to sustain this thermal window produces interfacial adhesive peel strengths below 2 N/mm when tested per VDI 2019, whereas correctly processed assemblies exhibit cohesive failure with peel values above 5 N/mm. The primary failure mode recorded on production lines is delamination at connector backshell radii below 2 mm, where local substrate cooling below 80°C suppresses interdiffusion kinetics and yields an adhesive interface. PBT substrate pre-drying at 120°C for 4 hours to a dew point of -40°C is mandatory before the first shot; residual moisture above 0.02% triggers hydrolysis of the polyester substrate, producing terephthalic acid oligomers that bloom to the surface and degrade second-shot bonding.

    Compliance for automotive electrical connector applications centers on ISO 6722-1:2011 (single-core cable insulation and sheath materials, clause 5.3 abrasion and clause 5.7 heat ageing), USCAR-2 Revision 7 (electrical connector performance specification including terminal retention force and seal integrity after thermal cycling from -40°C to 85°C), GMW 16090 (General Motors TPE material specification for overmolded electrical components), and LV 112 (Volkswagen electrical connector test specification, subsection 7.3 for seal material temperature excursion). REACH Regulation (EC) No 1907/2006 Annex XVII and RoHS Directive 2011/65/EU Annex II confirm SVHC concentrations below 0.1% w/w. The formulation addition ratio in downstream processing is governed by connector design envelope: the soft SEBS-PBT component typically occupies 15–40% of total molded part volume in multi-material assemblies, with seal lips designed at a compression ratio of 15–25% relative to free-state cross-section (measurable per ISO 48-4:2018 using an automated wall thickness gauge). Downstream production utilises two-shot rotary table injection molding with robotic insert extraction, melt temperature 220–245°C (air-shot pyrometer verification), mold temperature 40–60°C with cycled thermolator, and injection velocity 80–150 mm/s. End product types include IP67-rated electrical connector backshells, wire seal grommets for engine harness bulkheads, battery management system terminal covers, and charging port dust caps for electric-vehicle infrastructure.

    Where hydraulic valve sealing components are converted from thermoset nitrile rubber (NBR) or hydrogenated nitrile rubber (HNBR) to recyclable thermoplastic alternatives, SEBS-PBT compounds at 60 Shore A occupy a substitution window defined by compression set performance under mineral oil service. In hydraulic spool valve end caps, cartridge valve O-rings, and pneumatic regulator poppet seals, the PBT modification suppresses equilibrium volume swell in IRM 903 oil relative to unmodified SEBS by approximately 40–50% after 70-hour immersion at 100°C, as quantified per ASTM D471-16a using die-cut specimens from 2 mm compression molded plaques and equilibrium measurement at 168 hours for full saturation. Compression set after 22 hours at 70°C per ISO 815-1:2014 falls within 35–50% for SEBS-PBT 60 Shore A compounds, compared with 55–65% for neat SEBS at equivalent hardness. The two-component morphology is verified by dynamic mechanical analysis: two distinct loss modulus peaks appear near -45°C (ethylene-butylene midblock relaxation) and 45°C (PBT glass transition). Formulation addition ratio in downstream part design is 100% of seal cross-section—no diluent or secondary elastomer is compounded at converter level; the PBT content is pre-incorporated by the compound supplier to maintain processable phase domains. Downstream production involves reciprocating screw injection molding with melt temperature 220–245°C (measured by air-shot pyrometer), mold temperature 40–60°C, and hold pressure maintained until gate freeze-off at approximately 1.5–2.0 seconds for a 1 mm-thick gate. End product types include hydraulic valve stem seals, fuel pump diaphragm gaskets, oil-cooler gasket plates, and pneumatic regulator poppet seals for compressed air service at operating temperatures from -30°C to 110°C continuous.

    Chemical resistance profile for SEBS-PBT compounds at 60 Shore A (indicative ranges, converter-side verification recommended per production lot)
    Fluid mediumTest duration / temperatureHardness shift (Shore A, per ISO 48-4)Volume swell (%)Tensile strength retention (%, per ASTM D638-14 Type 5)
    IRM 903 mineral oil70 h / 100°C+5 to +1030–4575–85
    IRM 901 mineral oil70 h / 100°C+8 to +1545–6070–80
    ASTM Reference Fuel C (50% toluene / 50% isooctane)22 h / 23°C-25 to -3055–7550–60
    Deionized water168 h / 100°C±31–390–95
    10% NaOH aqueous solution168 h / 23°C±2<1>95

    What Limits Shot-to-Shot Dimensional Stability at 60 Shore A?

    Typically, power tool grip overmolding onto glass-fiber-reinforced PBT or PA6/6 housings exposes the SEBS-PBT compound to two competing stabilisation demands: vibration damping effectiveness at frequencies between 10 and 100 Hz and dimensional repeatability across 8–12-cavity insert molding tools. In production-scale vertical clamp insert molding cells (80–150 tonnes, rotary indexing table, dual bottom-half molds to retain insert temperature), shot-to-shot weight variation of the soft component must remain within 0.3–0.5% across a 50-shot validation block (checkweigher data) to prevent grip wall thickness drift outside the 1.5–3.0 mm specification band. The injection unit set temperature must remain within 220–235°C. Exceeding 260°C initiates β-hydrogen-transfer thermal degradation of the PBT segments, producing butadiene and tetrahydrofuran byproducts that attack residual catalyst in the SEBS phase. Extended residence time of 45 seconds at temperatures above 250°C—for example during an unplanned downstream machine stoppage—shifts melt flow index (ISO 1133-1:2022, 2.16 kg at 230°C) by more than 15% and correlates with field returns showing grip surface cracking after 500 hours of accelerated UV exposure (ISO 4892-2, cycle A, irradiance 0.51 W/m² at 340 nm). Industry compliance for power tool grips is anchored to IEC 60745-1:2006 (hand-held motor-operated electric tools—safety, clause 19 for mechanical strength of polymeric enclosures), UL 94 HB (horizontal burn test, clause 7.1: specimen 125 mm × 13 mm × 3 mm), and RoHS Directive 2011/65/EU Annex II. Vibration attenuation is assessed per ISO 5349-1:2001 (measurement of hand-transmitted vibration) with accelerometer transmissibility measured at the tool housing surface. The formulation addition ratio for grip overmolding ranges from 20–35% of total molded component mass; below 20%, the grip layer thickness falls under 1.5 mm and attenuation at 50 Hz degrades to less than 30%. Above 35%, shrinkage differential introduces visible sink on the opposite housing face. Downstream production uses robotic insert loading with substrate preheating to 80–100°C via infrared tunnel, injection speed 80–150 mm/s, and a two-stage holding pressure decay over 8–12 seconds. End product types include drill/driver overmolded soft-grip housings, angle grinder vibration-damped front handles, and pneumatic nail gun rear overgrips.

    Across oral-care and personal-care manufacturing lines, two-shot toothbrush handle production from SEBS-PBT compounds at 60 Shore A is constrained primarily by migration compliance rather than mechanical processing complexity. The PBT component, present at a lower fraction than in automotive overmolding grades, does not alter the fundamental regulatory framework: repeated-use food-contact compliance falls under FDA 21 CFR §177.2600 (rubber articles intended for repeated use, extraction limits for water and n-heptane per conditions of use), EU Regulation 10/2011 on plastic materials intended for food contact (overall migration limit 10 mg/dm² per EN 1186-1), and ISO 10993-5 (in vitro cytotoxicity, MTT assay) for oral cavity contact. For toothbrush and razor handle overmolding onto polypropylene or PBT cores, the SEBS-PBT 60 Shore A compound is injected as the 100% soft-component shot in a two-shot rotary machine (80–120 tonnes, L/D 20:1), with melt temperature 215–230°C and mold temperature 25–40°C. The PBT domains do not degrade adhesion to polypropylene substrates as long as the SEBS continuous phase remains dominant; peel adhesion values above 3 N/mm are consistently achieved on PP substrates at 60 Shore A without adhesive primers. The formulation addition ratio of the soft segment relative to the rigid core typically falls between 25% and 45% of total component volume. Grip zones thinner than 1.2 mm introduce flow-induced phase separation of the PBT domains, which appears as surface gloss variation—gloss units measured at 60° incidence per ISO 2813 deviate by more than 5 GU from nominal. End product types include manual toothbrush handles with soft-grip zones, razor cartridge head connectors, interdental brush handles, and electric toothbrush body grips.

    Thin-Wall Encapsulation Gate Freeze-Off Thresholds

    Consumer electronics cable overmolding at wall thicknesses below 1.0 mm exposes a specific processing limit in SEBS-PBT compounds: the freeze-off time of the gate relative to the packed melt front. For a hot-tip gate with melt channel diameter 1.2 mm feeding a 0.6 mm wall thickness sheath around a USB-C connector boot, gate freeze-off occurs within 0.8–1.4 seconds of switchover to holding pressure—meaning the hold phase contributes no further packing to material downstream of the gate. The result is sink marks exceeding the 0.03 mm surface deviation limit specified in consumer electronics OEM cosmetic drawings (measured by optical profilometry per ISO 25178-2) and visible knit-line artifacts where melt fronts recombine around the cable core. Mitigation on production lines requires gate diameter reduction to 0.6–0.8 mm to coordinate freeze-off with the packed melt front, and elevated melt temperatures of 230–245°C (pyrometer verification at nozzle tip) to maintain melt flow index above 8 g/10 min per ISO 1133-1:2022 (2.16 kg at 230°C). Apparent viscosity at 230°C and 1000 s⁻¹ shear rate falls within 80–150 Pa·s for SEBS-PBT 60 Shore A compounds, a rheological window that permits filling of wall thicknesses down to 0.5 mm at injection velocities of 150–250 mm/s without pressure-limited short shots. Industry compliance for this segment draws on IEC 62368-1:2023 (audio/video, information and communication technology equipment—safety, clause 6.4 for polymeric material in enclosures), UL 94 HB (for non-structural housings), and RoHS 2011/65/EU Annex II. The formulation addition ratio for thin-wall encapsulation is 100% as-supplied compound; when converted into hard-soft co-molded parts, the soft SEBS-PBT component typically comprises 15–25% of part volume. Downstream production deploys high-velocity servo-driven injection (acceleration from 0 to 0.4 seconds), mineral-oil-free mold release surfactant to avoid adhesion degradation for overmolding, and mold temperatures of 35–50°C. End product types include USB-C and Lightning connector cable strain reliefs, headphone cable entry boots, drone battery charger housing anti-impact lips, and wearable device strap attachment grommets.

    When Post-Mold Gamma Irradiation Replaces Ethylene Oxide Sterilization

    Because gamma radiation at 25–40 kGy generates free radicals in both the SEBS ethylene-butylene midblock and the PBT aromatic ring system, selection of SEBS-PBT 60 Shore A compounds for medical device housings and handheld diagnostic instrument grips is governed by terminal sterilization method. Gamma irradiation per ISO 11137-1:2015 (dose establishment, clause 4.3) initiates radical recombination in the SEBS phase that manifests as crosslinking: Shore A hardness increases by 3–5 units per ISO 48-4:2018, and elongation at break falls from above 400% to below 250% per ASTM D638-14 (Type 5 dumbbell, 100 mm/min crosshead speed) when no radiation-stable antioxidant package is incorporated. Compounds formulated for gamma stability exhibit post-irradiation hardness shift below 2 Shore A units and elongation retention above 85% at 40 kGy. Industry compliance for this segment historically prioritizes ISO 10993-1:2018 (biological evaluation of medical devices, clause 4.2 classification), ISO 13485:2016 (quality management for medical device manufacturing, clause 7.5 production and service provision, and clause 7.5.2 process validation), and USP <88> Biological Reactivity Class VI (injection and implantation extract studies). The formulation addition ratio of the SEBS-PBT 60 Shore A compound in medical device assembly typically falls between 10% and 30% of total part volume where overmolded onto rigid engineering thermoplastics (PBT, PC/ABS, or polysulfone); the soft component is molded at 100% of its own shot volume without diluent. Downstream processing involves Class 7 (ISO 14644-1) cleanroom injection molding, screw and barrel surfaces with electroless nickel plating to minimise metallic contamination, and process validation per IQ/OQ/PQ protocols documented under ISO 13485 clause 7.5.2. End product types include handheld ultrasound probe housings, blood glucose meter protective bumpers, surgical instrument grip sleeves, and diagnostic device carrying-handle cushions. Operational boundaries: ethylene oxide sterilization is compatible with SEBS-PBT 60 Shore A at standard EtO cycles (55°C, 6-hour exposure, followed by aeration to 0.1 ppm residual); autoclave steam sterilization at 121°C for 30 minutes exceeds the continuous service temperature of the SEBS phase and is not recommended without post-sterilization dimensional verification.

    Compliance standards matrix by downstream application sector for SEBS-PBT 60 Shore A compounds
    Application sectorPrimary standardTest designation / clauseAcceptance criterion (per standard)
    Automotive electrical connectorsUSCAR-2 Rev 7Terminal retention force; seal integrity after thermal cyclingNo terminal push-out below minimum retention force; no water ingress at specified pressure differential
    Industrial hydraulic sealsASTM D471-16aVolume swell, hardness shift after immersion≤50% volume swell in IRM 903 at 100°C/70 h; ≤+10 Shore A hardness shift
    Power tool gripsIEC 60745-1:2006Clause 19 mechanical strength; UL 94 clause 7.1No cracking after ball impact test; UL 94 HB classification
    Personal care / oral hygieneFDA 21 CFR §177.2600Extraction (water, n-heptane) under conditions of useExtractives below regulatory thresholds; overall migration ≤10 mg/dm² per EU 10/2011
    Consumer electronicsIEC 62368-1:2023Clause 6.4 enclosure polymeric material; UL 94 HBNo glow wire ignition; UL 94 HB classification
    Medical device housingsISO 10993-1:2018In vitro cytotoxicity (ISO 10993-5); extractables (ISO 10993-12)No cytotoxicity; USP <88> Class VI; post-gamma hardness shift ≤2 Shore A
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    Certification & Compliance
    More Introduction

    API Megol AM SEBS-Comp. DP2217/60PBT is a thermoplastic elastomer compound in which a styrene–ethylene/butylene–styrene block copolymer matrix is modified with a nominal 60 wt% polybutylene terephthalate hard phase, as indicated by the 60PBT grade suffix. The AM code is an internal API modifier designation, and the exact additive package is not publicly disclosed; grade-specific data should therefore be confirmed against the manufacturer certificate of analysis. This compound is positioned for injection molding and profile extrusion applications requiring higher heat deflection, improved dimensional stability, and greater resistance to aliphatic hydrocarbon fluids than conventional oil-extended SEBS grades. Published data for this specific configuration is limited; the ranges in this document are representative of 55–65 wt% PBT/SEBS compounds unless a product-specific certificate is cited.

    Morphologically, the system relies on a biphasic structure. The SEBS fraction contributes elastic recovery and low-temperature impact, while the dispersed or co-continuous PBT domains provide a melting point near 220–225 °C as measured by differential scanning calorimetry under ISO 11357-3. The styrene end blocks in SEBS act as physical crosslinks below their glass transition near 95 °C, whereas the ethylene/butylene midblock provides rubber-like segmental motion. The PBT component alters the tensile failure mode from ductile rubber tearing toward yielding or fibrillation at high deformation rates, as reflected in ISO 527-2 tensile tests. This structural shift is the central difference between DP2217/60PBT and fully elastomeric SEBS grades: the polyester phase introduces hard-segment crystallinity but reduces low-strain elasticity.

    When a 60 wt% Polyester Hard Phase Replaces Mineral-Oil Extension in SEBS Compounds

    Replacing low-molecular-weight paraffinic or naphthenic oil with a polyester hard phase changes the property balance. Conventional oil-extended SEBS grades typically exhibit Shore A hardness between 30 and 80, tensile stress between 3 and 12 MPa, and Vicat B50 softening below 90 °C; the PBT-laden compound shifts hardness into the Shore D range, typically 60–75, and raises Vicat B50 values to 140–180 °C under ISO 306. The trade-off is a reduction in ultimate elongation from values above 400% for oil-extended SEBS to approximately 90–250% for the polyester-modified system, and a stiffer flexural modulus in the range 700–1600 MPa under ISO 178. This property envelope is not a product-specific specification; it is a compound-class range for 55–65 wt% PBT/SEBS alloys and should be used only for tooling feasibility studies until the supplier certificate is obtained.

    Pre-drying of the pelletized feedstock is mandatory in humid production environments. Moisture levels above 0.02 wt%, determined by ISO 15512 coulometric Karl Fischer titration, can hydrolyse the PBT phase during plastication and produce surface splay, viscosity loss, and weld-line weakness. Drying in a dehumidified hopper dryer at 120 °C for 4 h with a dew point of −40 °C or lower is a conservative starting condition. Melt temperature should be maintained between 230 °C and 250 °C; barrel profile settings of 220 °C rear, 230 °C center, 240 °C front, and 245 °C nozzle are typical for injection molding machines with a 20:1 or 24:1 L/D screw and a compression ratio of 2.5:1 to 3.0:1. Screws with shear-free mixing elements are preferred because high shear can reduce PBT domain size and increase melt temperature, leading to ethylene/butylene midblock oxidation. Back pressure between 0.5 and 1.5 MPa and screw surface speeds below 0.2 m/s are typical start-up values. Mold temperature is usually held at 30–70 °C; the upper range improves PBT crystallization and surface replication, whereas the lower range preserves soft-touch tactility and shortens cycle time.

    How Does the PBT Fraction Modify Solvent Resistance and Creep Response?

    Solvent uptake in SEBS compounds is predominantly governed by the ethylene/butylene midblock affinity for non-polar oils. The addition of a polyester hard phase creates a barrier to aliphatic hydrocarbons and reduces mass swell in ASTM D471 reference fluids such as IRM 901 and IRM 903. In publicly reported SEBS/PBT alloys, volume swell after 70 h at 23 °C in IRM 901 oil is often reduced by more than 50% relative to oil-extended SEBS at equivalent hardness, although published data for DP2217/60PBT specifically is limited. Creep strain under constant load, measured by ISO 899-1, is similarly reduced because the PBT domains behave as a rigid discontinuous reinforcement, restricting long-range segmental flow of the SEBS matrix. Compression set under ISO 815-1, method A, at 70 °C for 24 h typically remains in the 45–70% range for polyester-rich SEBS compounds; this is generally higher than a high-quality peroxide-crosslinked TPV but lower than plasticized PVC at equivalent hardness. The compound should therefore be specified for static seals only after prototype testing at the upper service temperature.

    Automotive interior and exterior attachment components, appliance feet, power-tool overmolds, and cable-management fittings are candidate uses when the design requires a Shore D 60–75 surface with tactile damping. The polyester content improves paint adhesion and polar-substrate overmolding compared with purely aliphatic SEBS, but adhesion to polyolefins decreases. For two-component molding onto PC/ABS or PBT substrates, melt bonding is promoted by shared polar ester interactions; pre-drying is even more critical because molten PBT adjacent to moist SEBS can generate gas at the interface. Published adhesion values for this specific grade are limited; shear-lap specimens prepared according to ISO 527-2 on a 3 mm plaque should be validated for each substrate lot. Insert molding with metal bushings and threaded fasteners is feasible when the melt temperature is kept below 250 °C to avoid post-mold insert movement caused by differential shrinkage.

    Thermal Ageing, Hydrolytic Stability and Processing-Induced Degradation

    Long-term heat exposure of SEBS/PBT compounds involves two simultaneous ageing mechanisms: oxidative degradation of the ethylene/butylene midblock and hydrolytic chain scission of the PBT ester groups. Ageing in a forced-air oven under ISO 188 at 150 °C for 500 h may reduce tensile strength by 15–40% depending on stabilizer package; retention values below 50% often indicate insufficient drying or excessive regrind. PBT hydrolysis is accelerated when moisture exceeds 0.05 wt% and melt temperature exceeds 260 °C. Shot-to-shot viscosity drift on the production floor, with melt mass-flow rate increasing by more than 20% under ISO 1133-1 at 250 °C and 5 kg, is an early indicator of molecular-weight loss. Regrind levels above 30 wt% should be avoided in parts with living hinges, snap-fits, or ultrasonic welds unless testing verifies retention of elongation at break. The compound should not be blended with amine-based additives because amine species can accelerate polyester transesterification and reduce service life.

    Three processing failure modes are documented in production-scale trials with polyester-rich SEBS compounds. First, if the material is molded above 260 °C, the PBT phase begins to emit acetaldehyde and tetrahydrofuran at trace levels, and the SEBS midblock oxidizes, producing yellowing and a reduction in tensile strength. Second, if mold temperature is below 30 °C, the PBT phase quenches into a low-crystallinity state, reducing chemical resistance and increasing post-mold dimensional drift. Third, if wet pellets enter the feed throat, steam hydrolysis of PBT produces bubble formation at the part surface rather than in the core, because moisture boils during decompression and migrates to the flow front. These defects can be distinguished by optical microscopy: splay appears as silvery streaks on the surface, while unmelted PBT domains appear as white specks under 10× magnification. Such field observations explain why start-up sheets often specify a drying-time interlock and melt-pressure alarms.

    Property and standardSEBS/PBT 55–65 wt% PBTOil-extended SEBSEPDM/PP TPV
    Density, ISO 1183-1 (g/cm³)1.07–1.160.88–1.000.95–1.00
    Hardness, ISO 86860–75 Shore D30–80 Shore A70 Shore A–50 Shore D
    Tensile stress at break, ISO 527-2 (MPa)18–323–128–20
    Elongation at break, ISO 527-2 (%)90–250400–750200–500
    Flexural modulus, ISO 178 (MPa)700–160010–100100–400
    Vicat softening B50, ISO 306 (°C)140–180<9080–140
    Compression set 70 °C/24 h, ISO 815-1 (%)45–7040–7030–55

    What Equipment Modifications Are Needed for Stable Metering of a PBT-Filled SEBS Compound?

    Standard injection-molding machines with closed-loop process control can process the compound if the screw design avoids high-shear dispersive mixing. A three-zone screw with 24:1 L/D, 2.5:1 compression ratio, and a non-return valve clearance below 0.05 mm is typical. Hot-runner systems should use externally heated manifolds with minimum dead spots, because PBT can degrade during hold times above 5 min at 250 °C. Shut-off nozzles are preferred over open nozzles for high-cushion molding. Molds with projected area above 500 cm² require clamp forces of 1,000–2,000 kN, based on conventional 2–4 kN/cm² cavity-pressure requirements; thin-wall sections below 1.5 mm may require injection pressures of 80–120 MPa and fast fill speeds to prevent premature PBT crystallization. Capillary rheometry of PBT-modified SEBS compounds typically shows shear-thinning behavior with a power-law index between 0.25 and 0.45 at shear rates from 100 to 1,000 s⁻¹ and melt temperatures of 240 °C. At low shear rates the viscosity increase is more pronounced than in oil-extended SEBS, which can lead to gate blush or jetting if the injection velocity profile is too slow. Spiral-flow testing in a 2 mm channel at 240 °C and 80 MPa fills lengths of 200–350 mm for this material class. These values are compound-class observations, not a certified product-specific data set for DP2217/60PBT.

    Production-scale compounding on a 44:1 L/D twin-screw extruder with co-rotating elements and gravimetric feeders frequently shows melt-temperature excursions of 5–12 °C if the PBT feed fraction is increased beyond 62 wt%, due to viscous dissipation in the kneading blocks. Operators often reduce screw speed from 350 to 250 min⁻¹ and increase barrel cooling in the plastication zone to keep melt temperature below 250 °C. Injection molders receiving pelletized batches should verify melt mass-flow rate under ISO 1133-1 because lot-to-lot variation of ±10% can affect filling and flash in tools with valve-gated hot runners.

    Compared with copolyester elastomers of similar Shore D hardness, the SEBS/PBT compound typically shows lower tensile strength and lower heat distortion but better low-temperature impact because the ethylene/butylene midblock retains flexibility below −40 °C. Compared with aromatic TPU, the SEBS/PBT grade exhibits better hydrolytic resistance and lower density, though TPU provides superior abrasion resistance under ISO 4649. Compared with unfilled SEBS, the PBT-modified grade offers higher modulus and lower oil swell but requires stricter drying and narrower melt-temperature control. Direct material substitution should be based on prototype testing because published data for this specific configuration is limited.

    Regulatory documentation supplied with API Megol compounds generally covers REACH registration duties and RoHS Directive 2011/65/EU recast (EU) 2015/863 restrictions on lead, mercury, cadmium, hexavalent chromium, PBBs, and PBDEs. Food-contact suitability is not automatically conveyed by polymer class; FDA 21 CFR 177.1810 covers styrene block polymers and 21 CFR 177.1660 covers thermoplastic polyesters, but the finished article requires end-use migration testing under the relevant food-simulant conditions. The grade should be stored in sealed containers at 5–30 °C and re-dried after exposure to relative humidity above 60% for more than 8 h.

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