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Asahi Kasei Tufprene® SBS 315P

    • Product Name: Asahi Kasei Tufprene® SBS 315P
    • Factroy Site: Yinchuan, Ningxia, China
    • Price Inquiry: sales8@ascent-chem.com
    • Manufacturer: Ascent Petrochem Holdings Co., Limited
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    Specifications
    HS Code 763937
    Polymertype Styrene-butadiene-styrene block copolymer (SBS)
    Molecularstructure Linear
    Styrenecontent 30 wt%
    Butadienecontent 70 wt%
    Density 0.94 g/cm³
    Specificgravity 0.94
    Meltflowrate 3.0 g/10 min at 200°C and 5 kg
    Shoreahardness 75
    Tensilestrength 20 MPa
    Elongationatbreak 800%
    Modulusat300percentelongation 2.5 MPa
    Tearstrength 40 kN/m
    Vicatsofteningpoint 70°C
    Appearance White to off-white pellets or powder

    As an accredited Asahi Kasei Tufprene® SBS 315P factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Asahi Kasei Tufprene® SBS 315P is typically packaged in 25 kg bags, with 40 bags (1,000 kg net) per pallet.
    Container Loading (20′ FCL) Asahi Kasei Tufprene® SBS 315P is loaded in a 20′ FCL dry container, palletized bags, protected from moisture and heat.
    Shipping Asahi Kasei Tufprene® SBS 315P is a non-hazardous thermoplastic elastomer supplied as pellets. Ship in dry, ventilated conditions in 25 kg PE-lined bags or bulk containers. Protect from moisture, direct sunlight, and excessive heat; avoid contamination. No UN number or dangerous-goods classification is required. Keep packages sealed and handle with care.
    Storage Store Asahi Kasei Tufprene® SBS 315P in original, sealed packaging in a cool, dry, well-ventilated warehouse. Protect from direct sunlight, heat, moisture, and contamination. Keep away from ignition sources and avoid prolonged UV exposure. Maintain moderate ambient temperatures, do not stack excessively, and use first-in, first-out stock rotation to preserve product quality. Close containers after use and keep labels legible.
    Shelf Life Asahi Kasei Tufprene® SBS 315P typically has a shelf life of about two years under recommended cool, dry storage conditions.
    Application of Asahi Kasei Tufprene® SBS 315P

    In polymer-modified bitumen production, Tufprene 315P is incorporated as the discontinuous elastomeric network phase in a continuous bitumen matrix. The processing sequence on a conventional PMB line begins by heating a penetration-grade base bitumen conforming to EN 12591:2009, typically a 50/70 or 70/100 grade, to 175–185°C in a jacketed blend tank equipped with load cells. SBS 315P is metered into the hot bitumen at 3.0–5.0 wt% of total binder for dense-graded surface course and urban road specifications, while high-stress pavements such as signalised intersections, bus rapid transit lanes, and airport aprons are commonly compounded at 5.0–7.5 wt%. The addition ratio is not solely a function of final elastic recovery; it is constrained by the aromatic fraction of the base bitumen. When the bitumen aromatic content is insufficient to swell the styrene-butadiene-styrene midblock, the polymer remains visible as discrete gel particles in the milled binder. In those batches, an aromatic extender oil is introduced at 0.5–2.0 wt% of bitumen before polymer addition. The swollen mixture is allowed a residence time of 30–45 min and then passed through a rotor-stator colloid mill operating at 3,000–5,000 rpm with a shear gap of 0.25–0.50 mm. After milling, the binder is transferred to a maturation tank at 160–170°C and held under low-shear agitation for 60–120 min. If a sulfur-stabilised binder is specified, elemental sulfur is added at 0.05–0.15 wt% of bitumen only after dispersion is complete. Sulfur addition while the polymer phase is still in discrete milled domains causes uncontrolled crosslinking, a rapid viscosity rise, and a loss of ductilometer elastic recovery when tested according to ASTM D6084-18. The upper processing limit is 200°C; sustained operation above this threshold degrades the butadiene midblock, producing a viscosity decrease and an irreversible reduction in low-temperature flexibility. Compliance is assessed against EN 14023:2010 for polymer-modified binders in European supply contracts and ASTM D5976 or AASHTO M 320 for performance-graded binders in North American paving projects. Short-term ageing qualification uses ASTM D2872-22 rolling thin-film oven exposure to verify that the SBS network survives plant mixing, haul transport, and paving without excessive hardening. The terminal product is a polymer-modified binder supplied to hot-mix plants for dense-graded surface course asphalt, high-stress urban intersections, bus rapid transit corridors, and airport apron mixtures where elastic recovery and rutting resistance are specified at contract level. The most frequent production bottleneck on a PMB line is the formation of an undispersed polymer mass around the colloid mill inlet at high feed rate; the mill bypass loop is opened or the polymer feed paused before the mill differential pressure indicates a blocked inlet.

    What Controls the Melt Viscosity of SBS 315P in Hot-Melt Pressure-Sensitive Adhesive Compounding?

    Hot-melt pressure-sensitive adhesive compounding with Tufprene 315P requires balancing tackifier compatibility, melt viscosity, and thermal degradation under oxygen-limited mixing. The elastomer is charged at 15–25 wt% of the finished adhesive, with a hydrogenated hydrocarbon tackifier at 40–60 wt%, naphthenic or white mineral oil at 15–25 wt%, and a hindered phenolic antioxidant at 0.5–1.0 wt%. Higher Tufprene 315P loadings increase cohesive strength but also elevate melt viscosity beyond the capacity of low-shear hot-melt coating heads. Mixing is carried out in a 100–500 L sigma-blade kneader with thermal oil heating and a nitrogen purge across the vapour space. The resin is melted first at 150–160°C, SBS 315P pellets are added at a rotor speed of 20–25 rpm, and the oil is introduced in three or four increments rather than as a single charge to avoid phase separation and a sudden torque drop. Batch temperature is held at 145–165°C for 50–90 min; excursions above 180°C cause chain scission, viscosity drift, and gel formation from the unsaturated butadiene midblock, which appears as undispersed translucent specks in the coated film. Adhesive products intended for food packaging applications are evaluated under FDA 21 CFR 175.105 and, where coated paperboard is involved, FDA 21 CFR 176.170; tackifier, oil, and stabiliser selection must account for migration limits because the finished adhesive is not a monolithic article. For the European market, the adhesive and its ingredients are registered under REACH Regulation (EC) No 1907/2006, and substance-specific restrictions are checked in REACH Annex XVII. Application viscosity is normally specified as 5,000–15,000 mPa·s at 160°C when measured with a Brookfield Thermosel. Published data for Tufprene 315P in this exact tackifier system is limited; the cited ranges are industrial starting points for linear SBS grades of comparable styrene content rather than a single validated grade-specific curve. The finished hot melts are used in label adhesive coatings, carton sealing tapes, hygiene article positioning tapes, and removable note adhesives where high initial tack is required without solvent content.

    For direct injection-moulded TPR outsoles, Tufprene 315P serves as the base elastomer in filled styrenic formulations where abrasion resistance and processability are more important than oil-free clarity. A standard starting formulation uses SBS 315P at 100 phr, naphthenic oil at 20–40 phr, general-purpose polystyrene resin at 5–15 phr, calcium carbonate at 20–40 phr, and antioxidant at 0.5–1.0 phr; in this compound, the polymer content corresponds to roughly 45–55 wt% of the finished outsole material. Published data specific to Tufprene 315P in outsole compounds is limited; the formulation is an industrial starting range for linear SBS with similar bound styrene content. The compound is premixed in a high-intensity mixer, compounded in a twin-screw extruder with an L/D ratio of 40:1, barrel temperatures of 150–180°C, screw speed of 200–300 rpm, and distributive mixing elements rather than high-shear kneading blocks to limit midblock degradation. The pelletised compound is injection-moulded at a melt temperature of 170–190°C with a mould temperature of 25–45°C; the melt must not remain stagnant in the barrel above 200°C because the butadiene segments degrade and produce a sticky, low-viscosity melt with poor mould release. Hardness is specified at 55–75 Shore A according to ISO 868:2003, tear strength is measured by ISO 34-1:2022, and flex resistance is assessed by ISO 17707:2016. PAH restrictions under REACH Annex XVII entry 50 apply to the extender oil used in the compound and to the finished article supplied to the public because the outsole is a skin-contact rubber article. Terminal products include injection-moulded sandals, slippers, and lightweight unit outsoles for casual footwear.

    Solvent-borne Laminating Adhesive Performance under EU Solvent Emission Limits

    Solvent-borne adhesive production based on Tufprene 315P is limited to operations that can handle flammable solvents and comply with solvent emission controls under Directive 2010/75/EU. The elastomer is dissolved at 15–20 wt% solids in a solvent blend of toluene, hexane, and methyl ethyl ketone, with a tackifying resin at 8–12 wt% solids and the solvent portion forming the remaining 65–75 wt% of the wet formulation. Dissolution is carried out in a high-speed disperser with an explosion-proof motor and nitrogen inerting at 25–40°C; solvent addition is staged to prevent lumping, and the final viscosity is controlled at 2,000–5,000 mPa·s at 25°C. The solution is filtered through a 100–150 µm bag filter before packaging to remove gel particles and undissolved polymer skins. Published data specific to Tufprene 315P in this solvent ratio is limited; the ranges represent industrial starting points for linear SBS grades used in contact laminating. The adhesive is tested for non-volatile content, drying time, and bond strength under ASTM D816-06(2020) or an equivalent user specification, while European REACH Annex XVII restrictions on solvent classification and article residues are applied to the final formulated product. The terminal product is a brush- or spray-applied contact adhesive for bonding wood laminates, flooring underlayment, and construction panels, where open time and high initial grab derive from the SBS 315P network after solvent flash-off.

    When SBS 315P Is Selected for Torch-applied Bituminous Waterproofing Compounds

    Where a manufacturer selects Tufprene 315P for torch-applied bituminous waterproofing compounds, the compound design must account for the melt-flow behaviour of SBS and the need to maintain calender processability. In this application, SBS 315P is added at 8–14 wt% of the bitumen compound, with mineral filler at 20–30 wt%, and the blend is mixed in a low-shear paddle mixer at 150–180°C until the polymer network is fully swollen and no visible polymer particles remain. The hot compound is calendered onto a spunbond polyester reinforcement of 150–250 g/m² at 120–150°C to a finished thickness of 3–5 mm, with sand, polyethylene film, or mineral granules applied to the surface before cooling. If the SBS addition is below 6 wt%, low-temperature flexibility required for roof waterproofing is not reliably achieved; if the addition exceeds 15 wt%, compound viscosity can reduce calender line speed and increase the risk of thermal scorch at the heated roll surface. Product conformity is assessed against EN 13707:2004+A2:2009 for reinforced bitumen roof sheets and ASTM D6164/D6164M-21 for SBS-modified polyester-reinforced sheet materials, with low-temperature flexibility and dimensional stability tests performed according to the methods referenced in those specifications. The terminal product is a torch-applied waterproofing membrane supplied in rolls for flat roofs, concrete bridge decks, plaza decks, and below-ground waterproofing systems where a polyester carrier and an SBS-modified bitumen coating provide installation integrity and crack-bridging capability.

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    Certification & Compliance
    More Introduction

    Tufprene® SBS 315P is a linear styrene-butadiene-styrene block copolymer manufactured by Asahi Kasei Corporation. The grade contains approximately 31 wt% bound styrene and exhibits a specific gravity of 0.94 when determined according to ISO 1183-1:2019. Melt mass-flow rate measured under ISO 1133-1:2022 at 190°C and 2.16 kg load is approximately 15 g/10 min. On compression-molded sheet tested according to JIS K6251, typical tensile strength is 5.0 MPa, 300% modulus is 1.5 MPa, and elongation at break is 1100%. Hardness measured with a Type A durometer according to JIS K6253 is 65. The product is therefore placed in the low-modulus, high-flow segment of the Tufprene SBS family. The styrene end-blocks form glassy domains that act as thermoreversible physical crosslinks, while the butadiene mid-block provides elastomeric recovery below the glass transition of the styrene domains. This architecture allows melt processing like a thermoplastic material without a separate vulcanization step.

    What Distinguishes 315P from Higher-Tensile Tufprene Grades?

    Tufprene A and Tufprene 125 contain approximately 40 wt% bound styrene. The higher aromatic vinyl concentration increases the volume fraction of physically crosslinked polystyrene domains, which raises tensile strength and hardness at the expense of elongation and melt flow. Table 1 compares typical values drawn from Asahi Kasei technical literature; the values are not guaranteed specifications and should be revalidated against the lot certificate.

    PropertyTufprene 315PTufprene ATufprene 125
    Bound styrene (wt%)314040
    Specific gravity (ISO 1183-1:2019)0.940.960.96
    Hardness (JIS K6253 Type A)658589
    Tensile strength (JIS K6251, MPa)5.015.225.5
    Elongation at break (JIS K6251, %)1100760520
    Melt mass-flow rate (ISO 1133-1:2022, 190°C/2.16 kg, g/10 min)155.60.6

    The difference in melt flow between 15 g/10 min for 315P and 0.6 g/10 min for Tufprene 125 is operationally significant. A 315P-based compound can be injected or extruded at barrel temperatures 10–20°C lower than a Tufprene 125 compound of equivalent styrene content; however, published data for this specific configuration is limited, and the process window should be derived from capillary rheometry rather than generic transfer from other grades. Higher-styrene grades are typically specified when tensile strength must exceed 10 MPa; 315P is selected for applications that prioritize elongation, conformability, and ease of dispersion into nonpolar matrices.

    Thermal and Shear Limits in Melt Processing

    In melt-compounding operations, the butadiene segment is susceptible to oxidative chain scission and radical-induced gel formation when exposed to excessive heat and shear. For Tufprene 315P, a barrel profile of 150–190°C is typical for twin-screw compounding; die temperature should remain below 195°C to limit viscosity loss and surface melt fracture. A corotating twin-screw extruder with an L/D ratio of 40:1 to 44:1 and modular mixing elements is used to disperse hydrocarbon tackifier resins and process oils without excessive specific energy input. At screw speeds above 400 rpm, temperature overshoot of 15–25°C can develop due to viscous dissipation; this is a critical threshold when filler or high-vinyl tackifier raises compound viscosity. Pre-drying at 70°C for 2 h is applied only if packaging has been opened at relative humidity above 60%, because condensation on cold pellets can create microvoids in extruded profiles.

    Thermal stabilizers are required for prolonged melt residence. A hindered phenolic antioxidant at 0.1–0.3 wt% and an organophosphite secondary antioxidant at 0.1–0.2 wt% are sufficient for most single-pass compounding, but repeated heat histories require the addition of a thioester synergist. Unstabilized 315P should not be held above 190°C for extended residence, because longer residence times can produce measurable viscosity reduction and gel particles.

    In solvent-borne and hot-melt adhesive compounding, Tufprene 315P interacts with aromatic and aliphatic hydrocarbon tackifiers, rosin esters, and naphthenic process oils. Typical hot-melt formulations contain 20–35 wt% 315P, 40–55 wt% hydrogenated hydrocarbon tackifier, and 15–30 wt% process oil; the low melt viscosity of the polymer allows application temperature to be held near 160–170°C in slot-die coating heads. The tackifier softens the butadiene phase and shifts the viscoelastic plateau, increasing peel adhesion while reducing cohesive shear strength. Viscosity drift above 5000 mPa·s at 175°C in a production hot-melt tank is commonly associated with skin formation and char build-up; nitrogen blanketing and low free-oxygen headspace reduce this failure mode. JIS K6251 tensile data on the neat polymer understate adhesive performance because the compound modulus and tack are dominated by tackifier-polymer phase behavior rather than by the original styrene domain network.

    When 315P Is Substituted into a Bitumen Formulation

    In polymer-modified asphalt and bituminous membranes, the final morphology depends on mixing temperature, shear rate, and compatibility between the butadiene-rich phase and the maltene fraction. A high-shear mixer with tip speed above 15 m/s is commonly used at 175–185°C; mixing times of 45–90 min are typical. The polystyrene domains must be swollen but not fully dissolved. Full dissolution of the styrene domains at temperatures above 200°C removes the physical crosslink network and lowers the softening point measured under EN 1427. For bituminous roofing membranes, modification levels of 8–12 wt% are common; in road asphalt concentrates, levels of 3–5 wt% are used. Published data for the exact change in penetration and softening point is limited because asphalt source and maltene content dominate the response. Compared with Tufprene A, the 31 wt% styrene grade disperses more readily and produces a softer compound at equal addition level, but it contributes less high-temperature stiffness.

    Compounding of Tufprene 315P into general-purpose polystyrene or high-impact polystyrene produces a multi-phase blend in which the butadiene-rich domains act as stress concentrators and improve impact toughness. At addition levels of 10–20 wt% in general-purpose polystyrene, the melt viscosity ratio between the SBS and the matrix controls the final dispersed particle size; a corotating twin-screw extruder with a residence time below 60 s is normally sufficient to reach a stable dispersed morphology. Unlike styrene-ethylene/butylene-styrene block copolymers, Tufprene 315P retains unsaturation in the butadiene mid-block. This structural feature limits continuous service temperature in air to approximately 70–80°C and demands UV and antiozonant packages for exterior exposure, but it improves compatibility with hydrocarbon resins and lowers the processing temperature compared with fully saturated SEBS. Ozone cracking of unprotected stressed specimens is evaluated under ASTM D1149. In PVC modification, the butadiene phase can absorb plasticizer over time, and migration kinetics in polymer matrices must be characterized for the specific plasticizer used.

    Regulatory and safety assessment for Tufprene 315P is application-specific. The substance is registered under REACH as styrene-butadiene-styrene block copolymer, but a registration number does not establish food-contact or medical compliance. For adhesive applications, FDA 21 CFR 175.105 may apply only when the finished adhesive is tested for migration under the intended use conditions; no compliance statement should be inferred without extraction testing. RoHS Directive 2011/65/EU heavy metal restrictions apply to the finished article rather than the raw polymer. The product should not be incinerated below 800°C without adequate afterburning because incomplete combustion of butadiene copolymers can generate carbon monoxide and unsaturated hydrocarbon fragments. Packaging should be stored at temperatures below 30°C and away from direct sunlight to minimize surface oxidation and yellowing during storage. The addition of antiozonant wax and phenolic antioxidant is required for outdoor service, particularly in compounds with high tackifier content.

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