| HS Code | 994060 |
| Materialtype | SEBS (hydrogenated styrene-butadiene-styrene block copolymer) |
| Styrenecontent | 30 wt% |
| Density | 0.91 g/cm³ |
| Meltflowrate | 3.0 g/10 min (230 °C, 2.16 kg) |
| Shoreahardness | 65 |
| Tensilestrength | 25 MPa |
| Elongationatbreak | 500% |
| Modulusat100percent | 3.0 MPa |
| Modulusat300percent | 6.0 MPa |
| Vicatsofteningpoint | 80 °C |
| Volumeresistivity | 1.0E15 Ω·cm |
As an accredited Asahi Kasei Tuftec™ SEBS P1083 factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Asahi Kasei Tuftec™ SEBS P1083 is supplied in 25 kg moisture-resistant paper bags, palletized for shipment. |
| Container Loading (20′ FCL) | 20′ FCL dry container loading of palletized Asahi Kasei Tuftec™ SEBS P1083 bags under ambient conditions, secured and moisture-protected. |
| Shipping | Asahi Kasei Tuftec™ SEBS P1083 is shipped as non-hazardous thermoplastic elastomer pellets, typically in moisture-barrier bags or cartons on pallets. Transport and store in a cool, dry, ventilated area away from direct sunlight and moisture. Generally, no UN hazard class or dangerous-goods documentation is required; follow the SDS. |
| Storage | Store Asahi Kasei Tuftec™ SEBS P1083 in a cool, dry, well-ventilated area, away from direct sunlight, heat, sparks, flames, and strong oxidizers. Keep containers tightly closed and palletized; protect from moisture, dust, and physical damage. Maintain ambient warehouse temperatures and use first-in, first-out stock rotation. Avoid prolonged exposure to elevated temperatures or UV light. |
| Shelf Life | Asahi Kasei Tuftec™ SEBS P1083 typically has a 24-month shelf life when stored dry, cool, and sealed in original packaging. |
The brittle-to-ductile transition in polypropylene impact copolymer compounds is observed around a P1083 loading of 10 wt% when the dispersed SEBS domain size is fixed below 1.0 µm by shear in a co-rotating twin-screw extruder with 36:1–40:1 L/D and screw speed of 350–500 rpm. The recommended addition envelope is 5–20 wt%, with 10–15 wt% used for automotive door trim and appliance housing compounds that must satisfy low-temperature notched impact under ISO 179-1/1eA at -30 °C while retaining ISO 527-2 tensile modulus above 1,000 MPa. Barrel temperatures are profiled from 210 °C in the first zone to 230 °C at the die on a 25 mm laboratory line running 60–80 kg/h; scale-up to 75 mm production equipment requires reduced screw speed to prevent melt temperature excursions beyond 240 °C, beyond which localized shear zones produce PP chain scission and incipient degradation at the SEBS rubber-phase interface. Injection molding of the compounded granulate is performed at 190–220 °C barrel temperature and 30–50 °C mold temperature, with clamp pressure selected for projected cavity area; insufficient clamp force on large fascia tools has been observed in production trials as flash-induced notch sensitivity at the sprue gate. At loadings below 7 wt%, notched Charpy values remain below the ductile threshold at -30 °C; at loadings above 20 wt%, flexural modulus and heat distortion temperature under 0.45 MPa decline to levels unsuitable for structural retainers. Regulatory checks for automotive interior compounds include REACH 1907/2006 candidate list screening and OEM volatile organic compound specifications such as VDA 270 odor rating, while food-contact appliance parts are evaluated under EU 10/2011 migration limits if the compound enters kitchenware housing service. Terminal manufactured goods include bumper fascia, rocker panel closures, washing machine balance rings, and appliance control panels.
The PP continuous phase carries the mechanical load while P1083-rich domains absorb impact energy, but this morphology is not self-forming. If the twin-screw melt seal is not maintained during oil injection, viscosity variation shifts the dispersed domain size distribution beyond 1.5 µm, and batch-to-batch Charpy scatter increases measurably. For ultraviolet-exposed parts, P1083 does not by itself provide long-term outdoor stabilization; a carbon black or HALS package must be added because the saturated midblock is resistant to oxidation but the PP matrix remains susceptible to photo-initiated chain scission.
For hygiene side-panel film production, an oil-extended SEBS compound must remain drawable at 250–300 m/min without blocking on the chill roll or wrapping the air knife. A screened formulation contains 35–50 wt% Tuftec P1083, 10–20 wt% polypropylene homopolymer or random copolymer, 25–40 wt% white mineral oil, and 0.5–1.0 phr stabilizer; the P1083 addition ratio is held inside this band because excursions above 50 wt% create melt-phase immiscibility at the die lip when the PP crystalline network can no longer carry oil evenly to the film surface without surface bloom. Compounding is performed on a co-rotating twin-screw extruder with 40:1 L/D using downstream oil injection at barrel 6–8 to prevent screw slip in the plastication zone; pelletizing is completed by underwater die-face cutting at 190–220 °C melt temperature. Cast film extrusion uses a 0.5–1.0 mm die gap, chill roll temperature of 15–25 °C, and air-knife differential pressure sufficient to suppress bubble formation between die and roll. Basis weight is controlled at 15–25 g/m², tensile elongation is measured by ASTM D882 or ISO 527-2, and permanent set is evaluated by cyclic elongation to 200%. Regulatory compliance for hygiene stretch films is evaluated under EU REACH 1907/2006 and relevant EDANA NWSP methods for basis weight and air permeability; ISO 10993 testing is not automatically applied unless the film is converted into a skin-contact wound dressing or medical device border. Terminal finished product types include elastic side panels, waistbands, breathable backsheet films, and elastic ear tapes for disposable absorbent articles.
When a Shore A 55 overmolding compound is aged for 24 h at 70 °C under 25% compression, retained elastic recovery depends less on P1083 molecular weight than on white mineral oil volume fraction and the continuity of the PP subnetwork. For injection-molded soft-touch grips, Tuftec P1083 is added at 20–45 wt%, polypropylene homopolymer at 10–20 wt%, white mineral oil at 25–40 wt%, and a non-migrating antioxidant at 0.3–0.8 phr; hardness is adjusted from Shore A 35 to Shore A 75 by changing the oil-to-PP ratio rather than SEBS content alone. The compound is alloyed on a co-rotating twin-screw extruder with 36:1 L/D and oil injection after the melting zone, pelletized, and then injection-molded at 190–230 °C barrel temperature and 30–50 °C mold temperature. Two-shot overmolding onto PC/ABS or polyamide substrates requires mechanical interlock features because the SEBS-PP blend exhibits low intrinsic peel adhesion to polar engineering resins. The relevant test set includes ASTM D2240 Shore A hardness, ISO 37 tensile strength and elongation, ISO 34-1 tear strength, ISO 815-1 compression set at 70 °C/24 h, and ISO 177 plasticizer migration for oil-exudation resistance. In production, parts ejected at 45 °C surface temperature have shown lower de-mold deformation when the mold texture is kept at VDI 24 or finer; higher oil loadings reduce surface tack but increase the risk of creep in undercut features and of sticky ejector-pin buildup after sustained cycles. Regulatory compliance for consumer goods focuses on REACH 1907/2006, RoHS 2011/65/EU, and for oral-care handles FDA 21 CFR 177.2600 when the final article is intended for repeated skin and indirect oral contact; supplier extraction data remain mandatory before that status is asserted. Terminal finished product categories include power tool overmolds, toothbrush handle grips, personal grooming devices, and appliance dials.
Low-smoke, halogen-free jacketing formulations impose a dual constraint on P1083: the melt temperature must remain below 190 °C for ATH dehydration stability, while the capillary viscosity must stay low enough for 0.6 mm wall cable extrusion at 80–120 m/min. In this sector, Tuftec P1083 is used at 10–25 wt% of the compound as a flexibilizer and filler-wetting agent, combined with an ethylene-vinyl acetate or LLDPE matrix, 60–65 wt% magnesium hydroxide or ATH, and a silane coupling agent at 0.5–1.0 phr. The high mineral filler phase raises melt viscosity more than the SEBS phase, so P1083 is selected primarily to reduce pressure loss in the die land and improve filler dispersion rather than to raise low-temperature impact. Compounding is performed on a co-rotating twin-screw line with 52:1 L/D and multiple side-stuffing ports; fillers are introduced downstream to limit screw-element abrasion, while melt temperature is held at 170–185 °C by barrel cooling rather than high screw speed. The pelletized jacketing compound is extruded on a 90 mm, 25:1 single-screw cable line with a 1.2 mm die gap and 150/200/250 µm screen pack; melt temperature at the die is monitored by infrared to avoid localized ATH release. Flame and smoke performance is verified against IEC 60332-1-2, IEC 61034, EN 50267-2-3, and UL 62 flexible cord requirements. Grade-specific flame performance data for P1083 in these exact matrices are limited, so compound qualification is conducted by cone calorimeter screening under ISO 5660-1 before full cable burn tests. Regulatory compliance includes RoHS 2011/65/EU, REACH 1907/2006, and the European Construction Products Regulation EU 305/2011 where cables fall under harmonized standards. Terminal finished products include flexible cord jackets, electric vehicle charging cable sheaths, robotic cable insulation, and industrial control cable outer layers.
During pelletizing of high-oil footwear midsole compounds, the residual heat history after strand die cutting determines whether pellets block during silo storage and whether subsequent injection molding can feed uniformly. Tuftec P1083 is loaded at 20–35 phr with a polypropylene modifier at 10–15 phr, naphthenic or white mineral oil at 35–50 phr, precipitated calcium carbonate at 0–15 phr, and an antiblock additive such as erucamide at 0.2–0.5 phr. The P1083 addition is balanced against oil absorption capacity because the ethylene-butylene midblock reaches saturation at roughly 1.2–1.5 times oil-to-rubber ratio; beyond that threshold, free oil migrates to the pellet surface within 72 h of storage and creates screw slip at the injection-molding feed throat. Mixing is performed in a 75 L intermeshing internal mixer at 120–160 °C for 8–12 min, followed by single-screw transfer to a strand die and air-knife pellet cooling to below 35 °C before classification. Injection molding of midsoles and sandals uses barrel temperatures of 180–200 °C and mold temperatures below 25 °C to maintain a micro-textured surface that lowers gloss without secondary spray. Mechanical qualification for footwear compounds uses ISO 868 Shore A hardness, ISO 815-1 compression set at 23 °C and 70 °C, ISO 4649 DIN abrasion, and ISO 17707 flex resistance; density is measured by ISO 1183-1. Chemical compliance for footwear exported to the European market includes REACH 1907/2006 Annex XVII restrictions on polycyclic aromatic hydrocarbons and CPSIA for children’s footwear in the United States. Terminal finished product types include EVA-replacement midsoles, sport sandal straps, insole cushioning layers, and water-resistant casual footwear shells.
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The classification of P1083 within SEBS chemistry derives from a triblock architecture consisting of hard styrenic end-blocks and a saturated midblock containing ethylene and butylene repeat units. The saturation of the midblock eliminates the high-main-chain unsaturation characteristic of SBS, shifting failure mechanisms away from allylic hydrogen abstraction and toward oxidative pathways that require longer exposure to equivalent heat and ultraviolet flux. Specification control for P1083 includes styrene block content, diblock content, total extractable oil, melt flow rate, pellet dimensions, ash, and tensile set. Each value is reported on the certificate of analysis using the producer’s internal methods cross-referenced to ISO 1133-1:2022, ISO 2781:2008, and ISO 37:2017 where applicable. Secondary datasheets for P1083 occasionally omit diblock content; in that case the diblock fraction should be requested from Asahi Kasei because it influences hysteresis, high-temperature set, and compatibility with polyolefin matrices.
In compounding operations, P1083 is used where a hydrogenated styrenic elastomer must be processed on conventional thermoplastic equipment without sulfur vulcanization or peroxide cure. The material is metered into single-screw and twin-screw lines as a base elastomer or as a modifier in polyolefin compounds. In film and sheet extrusion, the barrel profile is set to soften the styrenic domains while limiting midblock degradation; common SEBS processing set-point ranges are 180 °C to 230 °C, but the exact profile for P1083 must follow its specific melt-flow and shear-heating response. In injection molding, clamp force must be sufficient to prevent flash, while mold shrinkage determined under ISO 294-4:2018 remains lower than that of many semicrystalline polyolefins. Field experience on production lines indicates that low-compression screw designs with controlled back-pressure reduce melt-temperature overshoot and improve shot-to-shot consistency.
Compounding P1083 on a co-rotating twin-screw extruder with L/D 40:1 or 44:1 requires control of specific mechanical energy input, residence-time distribution, and localized shear heating. Because SEBS is pseudoplastic, melt viscosity decays under high shear, but the viscous dissipation contribution depends on screw geometry, throughput, and screw speed. Barrel set points are commonly 190 °C to 230 °C, with the rear feed barrel held 10 °C to 20 °C lower to prevent pellet bridging and feed collar blockage. Degradation is detected by a rise in melt flow rate beyond the producer’s tolerance band, using ISO 1133-1:2022 as the comparative method. Venting at atmospheric or light vacuum reduces volatiles, but excessive vacuum may draw low-molecular-weight fractions from the melt and alter the effective molecular mass distribution. For P1083, published process data is limited; however, SEBS rheology indicates that over-dispersive screw elements with narrow disc clearances can generate melt-temperature overshoot and should be replaced with distributive mixing elements when the objective is dispersion without chain scission.
The selection of P1083 against other SEBS grades depends on the melt flow rate reported under ISO 1133-1:2022 with 2.16 kg at 230 °C. Capillary viscosity measured under ASTM D3835-16 at 200 °C, 220 °C, and 240 °C provides shear-viscosity curves used to design dies, runners, and extrusion screws. SEBS-type melts often display power-law indices below 0.6 at high shear rates, but the P1083-specific exponent should be obtained from the current datasheet or from laboratory capillary testing. The styrenic endblock content and molecular mass distribution influence the transition from shear-thinning to melt fracture. During profile extrusion, melt fracture can appear as sharkskin at or above a critical wall shear stress; die land length and die exit temperature are adjusted to shift the melt fracture threshold. Comparative data for P1083 against lower-styrenic SEBS grades may show a higher melt flow rate and lower energy input during injection molding, but the exact values are controlled by the manufacturer and must be verified against the current release.
In direct comparison with unhydrogenated SBS grades, P1083 exhibits lower remnant unsaturation in the midblock, which reduces the rate of oxidative chain scission during high-temperature processing and permits a wider processing window with lower yellowing in repetitive regrind passes. Against other SEBS grades with lower styrenic content, P1083 is distinguished by higher hardness and higher stiffness-related properties, with reductions in softness and elastic recovery at sub-zero temperatures. Against Tuftec M-series maleic anhydride-modified SEBS, P1083 lacks the pendant anhydride functionality used for adhesion to polar substrates; therefore, adhesion to polyamide, polyurethane, or metal substrates requires surface treatment or a reactive tie layer. Against crosslinked EPDM, P1083 offers re-processability and direct injection moulding, but its oil-gel strength and compression set at elevated service temperatures may fall outside the range required for some dynamic seals.When P1083 is evaluated as an impact modifier in polypropylene or polyethylene compounds, its dispersion morphology is established during twin-screw compounding. The balance between styrenic endblock content and melt flow controls domain size; an excessively high melt-flow modifier can produce rounded elastomer domains that are too small to initiate shear yielding, while a low melt-flow grade can segregate at the surface during injection molding. In practice, the addition level is usually 5 wt% to 30 wt%, depending on the impact target and matrix melt-flow. Impact performance is measured by notched Izod or notched Charpy according to ISO 179-1:2020, ISO 180:2023, or ASTM D256-23. Tensile properties are evaluated under ISO 527-2:2012 using 1A or 5A specimens. The reduction in flexural modulus at each addition level is the primary trade-off; published data for P1083 in this specific configuration is limited, but similar hydrogenated styrenic block copolymers tend to reduce flexural modulus by 15% to 40% at modifier loadings of 15 wt% to 30 wt%.
Oil extension of P1083 is commonly performed to reduce hardness and increase elongation. The saturated midblock accepts paraffinic and naphthenic oils more readily than aromatic oils, because aromatic oils migrate slowly and may plasticise the styrenic end-blocks, reducing heat resistance and increasing compression set. The practical oil-absorption limit is reached when the compound exhibits surface oil bloom or when tensile properties fall below the target specification under ISO 37:2017. Oil loading is typically assessed by thermogravimetric oil loss under ISO 11358-1:2022 or by accelerated ageing at 100 °C for 72 h, followed by visual inspection for exudation. In high-oil compounds, batch-to-batch variance in oil uptake can shift hardness by several points; gravimetric feeders with mass-flow validation are used to keep oil content within tolerance. Published data for P1083 oil absorption at high loadings is limited; the producer’s compounding guideline should be followed before scaling to production.
Compression set of P1083 compounds is measured under ISO 815-1:2014 or ASTM D395-18 using type B specimens. The test conditions, typically 70 °C for 22 h or 100 °C for 22 h, depend on the intended service environment. Tension set is measured under ISO 2285:2013 after extension to a defined strain. Higher styrenic endblock content generally increases compression set at elevated temperatures because the hard domains lose load-bearing capacity as the glass transition region is approached. Dynamic mechanical analysis under ISO 6721-1:2019 identifies the temperature at which the plateau modulus declines. For P1083, the temperature and breadth of this transition should be obtained from the current datasheet; the grade-specific loss modulus peak and storage modulus onset are more useful than a single softening point for selecting service limits.
Medical and healthcare component trials evaluate P1083 against USP Class VI or ISO 10993-5:2009 and ISO 10993-10:2010 where the finished device is subject to cytotoxicity and skin sensitisation testing. The raw polymer is not a medical-grade approval; biocompatibility is established on the final sterilised device, not on the unfilled pellet. Compatibility with gamma irradiation and ethylene oxide must be validated, because styrenic domains can yellow under gamma exposure above 25 kGy to 50 kGy; published data for P1083 under terminal sterilisation is limited. For external device housings and hand grips, autoclave exposure at 121 °C may exceed the upper service limits of standard SEBS unless the part is load-light and the cycle is shortened. In any regulated application, the manufacturer’s food-contact or bioburden documentation should be obtained before commercial use.
Pellets are supplied with low moisture due to the hydrophobic nature of the saturated midblock, but storage in humid warehouses above 60% relative humidity creates surface adsorption. Pre-drying at 70 °C to 80 °C for 2 h to 4 h using a desiccant dryer with a dew point below -20 °C is standard for SEBS. Avoid combination with amine-based additives where contact clarity, food-contact organoleptics, or UV stability is critical, because amine migration can produce surface deposits and interfere with adhesion. Strong oxidizers and high levels of organic peroxide can initiate crosslinking of the saturated midblock and raise viscosity uncontrollably. Paraffinic or naphthenic oils are selected based on solvency and volatility; oil loading is controlled by the producer’s compatibility window. Batch-to-batch variance in pellet size and residual dust can affect feed consistency on single-screw machines with shallow feed pockets; a gravimetric feeder with overhead screw supply reduces feed pulsation.
Regulatory compliance for P1083 must be confirmed against the specific grade and production site. The table below lists standards and regulations commonly referenced for SEBS products.
| Measurement or requirement | Reference standard or regulation | Typical application relevance |
|---|---|---|
| Melt mass-flow rate | ISO 1133-1:2022 | Injection molding and extrusion process design |
| Hardness | ISO 868:2003 | Part feel and load distribution |
| Tensile stress-strain | ISO 37:2017 | Elastomeric product strength |
| Density | ISO 2781:2008 | Cost per volume and float behaviour |
| Mold shrinkage | ISO 294-4:2018 | Tool dimensions |
| Compression set | ISO 815-1:2014 or ASTM D395-18 | Seal and gasket recovery |
| Food-contact status | FDA 21 CFR 177.1810 or EU Regulation 10/2011 | Food packaging and kitchen tooling |
| Heavy metal restrictions | EU RoHS Directive 2011/65/EU | Electronics and appliance components |