| HS Code | 276690 |
| Productname | Asahi Kasei Tuftec™ SEBS P1500 |
| Polymertype | Hydrogenated styrene-butadiene-styrene block copolymer (SEBS) |
| Chemicalstructure | Styrene-ethylene/butylene-styrene block copolymer |
| Styrenecontent | 30 wt% |
| Density | 0.91 g/cm³ |
| Meltflowrate | 3 g/10 min at 230°C/2.16 kg |
| Hardness | Shore A 70 |
| Tensilestrength | 20 MPa |
| Elongationatbreak | 600% |
| 300percentmodulus | 5 MPa |
| Appearance | White powder or pellet |
| Processingmethods | Injection molding, extrusion, compounding |
As an accredited Asahi Kasei Tuftec™ SEBS P1500 factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Asahi Kasei Tuftec™ SEBS P1500 is supplied in 20 kg net moisture-barrier paper bags, palletized for bulk shipment. |
| Container Loading (20′ FCL) | 20′ FCL container loaded with Asahi Kasei Tuftec™ SEBS P1500 in sealed bags, palletized, evenly distributed, and securely stowed for transport. |
| Shipping | Asahi Kasei Tuftec™ SEBS P1500 is typically shipped as solid pellets in moisture-barrier bags or bulk sacks on pallets. It is generally not classified as dangerous goods for transport. Keep packaging sealed, dry, cool, and protected from UV, heat, and contamination until use. |
| Storage | Store Tuftec™ SEBS P1500 in a cool, dry, well-ventilated area, away from direct sunlight, heat, ignition sources, and moisture. Keep containers closed, undamaged, and in original packaging on pallets to prevent contamination. Protect from physical damage and avoid prolonged high temperatures. Follow the manufacturer’s SDS and local regulations, and use first-in, first-out stock rotation. |
| Shelf Life | Shelf life is typically 24 months when stored unopened in a cool, dry, well-ventilated place, away from sunlight and heat. |
In a co-rotating twin-screw compounding line running polypropylene homopolymer at barrel temperatures of 200–230 °C, Tuftec™ SEBS P1500 is introduced at 5–15 wt% to shift notched impact failure from brittle crack propagation to ductile yielding. The polypropylene carrier typically has a melt flow rate of 10–20 g/10 min at 230 °C, 2.16 kg. Melt temperature is controlled below 240 °C to limit degradation of the saturated ethylene-butylene midblock; residence time is held between 45 s and 90 s. Formulations for automotive interior impact modification are qualified under ISO 527-2 for tensile properties and ISO 179-1/1eA for Charpy notched impact at 23 °C and -20 °C. Regulatory conformance for EU automotive parts requires REACH SVHC below 0.1 wt% and RoHS Directive 2011/65/EU Annex II restrictions, including lead below 1000 mg/kg and cadmium below 100 mg/kg. The compounded strand is water-cooled at 30–40 °C and pelletized; subsequent injection molding of finished parts uses mold temperature 25–50 °C, injection pressure 25–35 MPa, and packing pressure 10–20 MPa. Finished part types produced from this configuration include door panel lower supports, pillar trim retainers, battery bracket housings, and interior clip assemblies.
Addition of SEBS P1500 at 10–25 wt% into an SIS/tackified hot-melt pressure-sensitive adhesive increases shear adhesion failure temperature as measured by ASTM D4498-07 because the high-molecular-weight styrene–ethylene–butylene block network restricts cold flow at temperatures above 45 °C. A starting formulation for transfer tapes and foam bonding adhesives contains 18 wt% SEBS P1500, 50 wt% C5/C9 hydrocarbon tackifier, 27 wt% naphthenic oil, and 5 wt% hydrogenated tackifier; loop tack is assessed by ASTM D6195-03, and 180° peel adhesion by ASTM D3330. If the adhesive is used in food packaging, components are selected to meet FDA 21 CFR 175.105 for adhesive overprint and lamination; EU 10/2011 overall migration limit of 10 mg/dm² applies for EU food-contact articles. Mixing is performed in a sigma-blade kneader or co-rotating twin-screw extruder at 160–180 °C; coating is carried out with a slot-die set at 150–170 °C at coat weight 20–40 g/m² onto a silicone-coated release liner. Spray coating is not recommended below 160 °C because the SEBS P1500 network raises melt viscosity sufficiently to destabilize helical spray patterns. Finished adhesive forms include double-coated tape, transfer tape, hygiene assembly adhesive, and foam bonding adhesive.
Because magnesium hydroxide releases water above 190 °C, barrel zone settings for SEBS P1500/Mg(OH)₂ compounds are held at 160–190 °C, with screw speed 300–400 min⁻¹ in a co-rotating twin-screw extruder with L/D 48:1. Filler is side-fed at barrel zone 5 of 10 to limit viscosity rise; dispersed magnesium hydroxide median particle size is 1.0–1.5 µm. Typical compound composition includes SEBS P1500 at 20–30 wt%, magnesium hydroxide at 50–60 wt%, polyethylene or polypropylene at 5–10 wt%, paraffinic oil at 5–10 wt%, silane coupling agent at 1.0–2.0 wt%, and antioxidant at 0.2–0.5 wt%. Low-smoke zero-halogen performance is assessed by IEC 60754-1 for halogen acid gas, IEC 60754-2 for pH and conductivity, IEC 61034-2 for smoke density, and IEC 60811-501 for tensile properties of sheathing compounds. Underwater pelletizing and drying to <0.05 wt% moisture precede cable jacket extrusion at 160–190 °C; line speed is adjusted to maintain melt pressure below 250 bar. If low-temperature service below -25 °C is specified, brittleness temperature should be verified under ASTM D746. Finished jacket types include outer sheathing for AC/DC EV charging cables, insulation jacketing for solar photovoltaic cables, control cable sheaths, and appliance internal wire coverings.
At a dosage of 3–7 wt% based on total bitumen mass, SEBS P1500 is pre-swollen in penetration-grade bitumen at 160–170 °C before high-shear mixing at 180–190 °C in a rotor-stator homogenizer for 45–90 min. The resulting polymer network modifies the viscoelastic response; softening point is measured per EN 1427, elastic recovery per EN 13398, and penetration per EN 1426. PMB specification compliance is assessed under EN 14023:2010; storage stability is evaluated by the difference in softening point between upper and lower samples after 72 h at 160 °C. For heavy-duty road binder, the addition ratio is typically 4–6 wt%; for waterproofing membrane compounds, SEBS P1500 can be increased to 6–7 wt% when bitumen with penetration 50–70 dmm is used. Unlike unsaturated SBS, SEBS P1500 does not require sulfur cure; physical endblock association provides network stability. Published data for P1500-specific low-temperature ductility in PMB remains limited; pilot blending is required when service temperatures below -10 °C are specified. Finished product types include bridge deck waterproofing membranes, heavy-traffic road binders for intersections, airport apron pavements, and self-adhesive roofing membrane base compounds.
Directly after pelletization, SEBS P1500-based compounds formulated for overmolding are injection-molded onto glass-filled nylon or polycarbonate substrates at a melt temperature of 190–220 °C; mold temperature is held at 25–50 °C to solidify the styrene domains rapidly. Hardness is measured per ISO 868 and falls in the range 45–65 Shore A; tensile properties are measured per ISO 527-2. For toy or child-use articles, EN 71-3 migration limits for soluble elements apply. Compound composition includes SEBS P1500 at 25–40 wt%, paraffinic white oil at 20–30 wt%, polypropylene at 15–20 wt%, mineral filler at 0–10 wt%, and antioxidant at 0.2–0.5 wt%; compounding uses a co-rotating twin-screw extruder with L/D 44:1, oil injection at barrel zone 4, and side-fed filler to prevent screw slip. Nylon substrates are dried to <0.15 wt% moisture before overmolding; polycarbonate substrates are dried to <0.02 wt%. Injection molding uses clamp force 500–1500 kN and packing pressure 10–20 MPa. Finished product types include cordless drill overmold grips, toothbrush handles, kitchen utensil handles, and protective corner overmolds on consumer electronics.
When migration testing under 21 CFR 177.1810 is performed on oil-extended SEBS P1500 tubing compounds, total extractives must remain within the limits specified for the intended food type and use temperature. For aqueous and fatty food contact below 80 °C, the compound is formulated with SEBS P1500 at 60–80 wt%, white mineral oil at 15–25 wt%, polypropylene at 5–15 wt%, and antioxidant at 0.1–0.3 wt%; oil loading is shifted to the low end for continuous fatty food contact above 60 °C. EU 10/2011 overall migration limit of 10 mg/dm² and specific migration limits for additives apply if the article is placed on the EU market. Tubing is extruded on a single-screw extruder with L/D 30:1, barrel profile 180–210 °C, and vacuum venting at -0.08 MPa; post-extrusion annealing at 80 °C for 2 h stabilizes dimensional tolerance. Gasket rings are injection-molded with mold temperature 30–50 °C. Finished product types include beverage transfer tubing, gasket rings for kitchen appliance closures, cap liners for dairy packaging, and cold-water dispenser seals.
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Asahi Kasei Tuftec™ SEBS P1500 is a hydrogenated styrene-ethylene/butylene-styrene block copolymer supplied as low-dust pellets. The P1500 designation appears in extrusion and compounding specifications where a saturated midblock is required for oxidative stability and retention of elastic recovery after thermal aging. The triblock architecture contains terminal polystyrene blocks that act as reversible physical crosslinks below the glass-transition temperature of the styrene phase, while the ethylene/butylene midblock supplies strain recovery and low-temperature flexibility. Polymer suppliers typically characterize this grade by melt flow rate using ISO 1133-1:2022 and by tensile properties using ISO 37:2017, but the final mechanical response is controlled by the dispersed styrene domain size and orientation after high-shear processing.
Hydrogenation of the butadiene midblock converts residual allylic double bonds into ethylene/butylene sequences, reducing the concentration of abstractable allylic hydrogen atoms. In circulating-air oven aging performed according to ISO 188:2023, saturated SEBS grades such as P1500 typically retain more tensile strength than unhydrogenated SBS after 168 h at 100 °C, although the exact retention depends on additive package and specimen geometry. Oxidation induction time measured by differential scanning calorimetry under ISO 11357-6:2018 is used as a rapid screening index for incoming resin or compounded pellets. The saturated midblock also reduces yellowing after multiple heat histories; yellowness index can be tracked by ASTM D1925.
The processing consequence of midblock saturation is not uniformly favorable. Although unsaturated SBS may build viscosity through crosslinking during repeated extrusion, saturated SEBS can undergo localized chain scission and gel formation if the melt exceeds the recommended temperature limit. The resulting gels appear as surface specks or hard particles in thin cast film, so control of melt temperature is more important than screw speed alone.
Compounding of P1500 is generally performed on co-rotating twin-screw extruders with screw diameters between 25 mm and 75 mm and length-to-diameter ratios of 36:1 to 52:1. A typical profile includes a feed-zone set point of 130 °C to 140 °C, a mid-barrel set point of 190 °C to 210 °C, and a die set point of 200 °C to 220 °C. Use of a gear pump is common because the melt has high elasticity and therefore unstable open-discharge behavior. Screen changers with 80/120/80 mesh packs reduce melt defects; however, excessive screens can raise melt temperature above safe limits. Melt temperatures above 240 °C should be avoided because thermo-oxidative degradation of the styrene end-blocks can generate gel particles and reduce elongation. Drying at 70 °C to 80 °C for 2 h to 4 h in a desiccant dryer is recommended when ambient relative humidity exceeds 60%.
The melt flow rate determined at 230 °C under 2.16 kg load according to ISO 1133-1:2022 places P1500 in the high-viscosity region of the styrenic block copolymer range. This restricts melt intrusion into thin-wall sections but improves shape retention in profile extrusion and orientation maintenance in cast film. Shear-thinning behavior is pronounced; capillary rheometry according to ISO 11443:2021 is used to map viscosity for die design and to establish pressure limits on downstream melt pumps. Moisture content in pellets should be maintained below 0.1% by mass, measured by ISO 15512:2019, before vented or unvented processing lines are started.
Injection moulding of straight P1500 is performed with barrel temperatures from 170 °C to 220 °C and mould temperatures from 20 °C to 50 °C. Because the melt is highly elastic, gates are typically limited to round or fan geometries with short land lengths, and mould surfaces may require micro-texturing to prevent vacuum adhesion during ejection. Clamp force requirements follow from the projected area and cavity pressure; the material does not require tonnage above that expected for unfilled styrenic TPE compounds.
EPDM requires either sulfur or peroxide cure, which adds formulation complexity and prevents direct re-extrusion of edge trim. Substitution with P1500 removes vulcanization kinetics from the production line and permits melt recycling of clean scrap. On a 60 mm single-screw extruder with L/D 30:1, line speed in seal extrusion is limited by cooling-bath length and gear-pump pressure rather than cure time. Compression set measured according to ASTM D395-18 Method B remains higher than that of crosslinked EPDM; the difference is usually material- and compound-specific, and published data for this exact P1500/EPDM comparison is limited. The trade-off is thermal service temperature: because the styrene domains soften near 100 °C, P1500 is not a direct replacement for EPDM in continuous exposure above 120 °C unless the compound is highly filled or dynamically vulcanized.
In weather-sealing compounds, P1500 is often extended with paraffinic oil and blended with polypropylene. Oil addition above 50 phr typically produces a sharp decrease in tensile strength and 100% modulus; above 70 phr, oil bleed may appear unless a crystalline polypropylene phase is present. Oil composition and aromatic content should be checked by ASTM D3238 or supplier certificate, as high-aromatic oils soften the styrene domains disproportionately.
The following ranges summarize publicly available Tuftec P-series literature values rather than contractual acceptance limits. Lot-specific values may differ, and the batch certificate should govern release decisions.
| Property | Test method | Published range |
|---|---|---|
| Density | ISO 1183-1:2019 / ASTM D792-20 | 0.90–0.92 g/cm³ |
| Hardness | ISO 48-4:2018 / ASTM D2240-15e1 | Shore A 60–80 |
| Tensile strength at break | ISO 37:2017 / ASTM D638-14 | 12–22 MPa |
| Elongation at break | ISO 37:2017 / ASTM D638-14 | 500–800 % |
| 100% stress | ISO 37:2017 / ASTM D412-16 | 2.0–3.5 MPa |
| Melt mass-flow rate | ISO 1133-1:2022 (230 °C, 2.16 kg) | 0.4–1.5 g/10 min |
| Styrene content | Asahi Kasei internal specification | 28–35 wt% |
For food-contact sealing applications, the final compounded article is typically evaluated under FDA 21 CFR 177.2600 for rubber articles intended for repeated food-contact use and under Commission Regulation (EU) No 10/2011 when the article is classified as plastic. P1500 is not supplied as a standalone medical-grade material; medical components require validation under ISO 10993-5 and ISO 10993-10. The unsaturated precursor or additives introduced during compounding may require additional REACH compliance documentation under Regulation (EC) No 1907/2006.
Compared with unhydrogenated Tufprene SBS grades, P1500 exhibits lower tack and lower zero-shear tack in pressure-sensitive adhesive formulations but better ultraviolet and thermal aging. Compared with higher-styrene Tuftec grades, P1500 has a softer response and higher elongation when compounded at fixed oil content. Compared with ester-based TPU, density is lower and hydrolytic stability in hot-water immersion is improved, but tensile strength and abrasion resistance measured by ISO 4649:2017 are lower. Published side-by-side data with other Asahi Kasei grades under identical ASTM D638-14 conditions are limited.
Gel formation in P1500 compounds is often traced to dead spots in screen changers, high local shear at kneading blocks, or prolonged residence time above 220 °C. On a 50 mm co-rotating twin-screw line with L/D 48:1, placement of distributive mixing elements after the oil-injection port and before the vent section has been used to improve dispersion without excessive temperature rise. Melt filtration through 100 µm or 200 µm mesh improves film clarity but increases backpressure; the pressure drop should be monitored with a melt-pressure transducer to avoid surpassing the extruder thrust bearing limit. Published data for the exact gel-count reduction on P1500 is limited, but processor reports indicate that reducing melt temperature by 10 °C can lower visual gel density in cast film more effectively than increasing screen mesh.