| HS Code | 378774 |
| Chemical Type | styrene-butadiene-styrene block copolymer (SBS) |
| Polymer Structure | linear triblock |
| Styrene Content | 30 wt% |
| Density | 0.94 g/cm³ |
| Melt Flow Rate | approx. 3 g/10 min (200 °C, 5 kg) |
| Shore A Hardness | approx. 72 |
| Tensile Strength | approx. 20 MPa |
| Elongation At Break | approx. 700% |
| Modulus At 300 Percent | approx. 3.0 MPa |
| Solution Viscosity | approx. 2.0 Pa·s (25 wt% in toluene, 25 °C) |
| Volatile Matter | ≤0.5 wt% |
| Ash Content | ≤0.1 wt% |
| Antioxidant Content | present |
| Appearance | white to off-white pellets |
As an accredited Asahi Kasei Asaprene™ SBS T-413 factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Asahi Kasei Asaprene™ SBS T-413 is packaged in 25 kg net paper bags with polyethylene liners, palletized for shipment. |
| Container Loading (20′ FCL) | 20-foot FCL container loaded with Asahi Kasei Asaprene™ SBS T-413, securely palletized, shrink-wrapped, and stowed for safe ocean freight. |
| Shipping | Asahi Kasei Asaprene™ SBS T-413 is a solid styrene-butadiene-styrene block copolymer typically shipped in moisture-barrier bags or cartons on pallets. It is not regulated as dangerous goods for transport. Store in a cool, dry place away from heat, sunlight, and moisture; handle with standard industrial hygiene. |
| Storage | Store Asahi Kasei Asaprene™ SBS T-413 in a cool, dry, well-ventilated area away from direct sunlight, heat, ignition sources, and oxidizing materials. Keep containers tightly closed to prevent moisture and contamination. Avoid prolonged exposure to elevated temperatures and UV light. Use first-in, first-out stock rotation, and maintain clean, dry handling and storage conditions. |
| Shelf Life | Asahi Kasei Asaprene™ SBS T-413 typically has a 12-month shelf life from manufacture when stored in original, unopened packaging in a cool, dry place. |
In hot-melt pressure-sensitive adhesive compounding, Asahi Kasei Asaprene™ SBS T-413 is introduced as the predominant styrenic triblock elastomer at 18–32 wt% of the finished adhesive mass, with 40–55 wt% hydrogenated C5/C9 tackifier resin and 15–25 wt% naphthenic or paraffinic process oil; antioxidant loading is maintained at 0.5–1.0 wt% to suppress oxidative gel formation during extended pot life. The applicable food-contact adhesive boundary is FDA 21 CFR 175.105 for indirect food contact, with REACH EC 1907/2006 applying to EU import. Production-scale melt blending is performed in a 200–300 L sigma-blade kneader with heated jacket or a 40:1 L/D co-rotating twin-screw extruder with barrel zones set to 140/150/160/170/165 °C; SBS T-413 is charged only after the resin and oil phase reaches 140 °C to avoid excessive initial torque. The styrene endblock network dissipates at rotor tip speeds of 1.5–2.5 m/s, and residence time above 170 °C is held to 45–60 min to limit chain scission; intermeshing kneading blocks are specified for at least 30% of screw length because insufficient styrene microphase dissolution below 140 °C produces low-frequency melt fracture at the coating die. Terminal adhesive articles include high-speed label stocks, carton sealing tapes, diaper frontal tapes, and removable protective films; peel adhesion is evaluated under ASTM D3330/D3330M-04 and loop tack under PSTC-16, while hot-melt viscosity is measured by ASTM D3236 at 160 °C. Full-scale batches exhibit viscosity drift greater than ±10% when jacket temperature exceeds 175 °C or when air contact is not blanketed; nitrogen overlay and continuous melt filtration through 200-mesh screens are therefore standard at the coating line.
Production of SBS-modified bitumen roofing membranes begins with oxidation-grade bitumen heated to 160–180 °C in a jacketed mixer; SBS T-413 is then metered at 8–14 wt% of total binder and dispersed in a Silverson-type rotor-stator mixer with square-hole screen at 2,500–4,000 rpm for 60–120 min. The resulting polymer-bitumen network is specified under EN 13707:2004+A2:2009 for flexible sheets for roof waterproofing and ASTM D6164/D6164M-21 for SBS-modified bituminous sheets, with ring-and-ball softening point tested to ASTM D36/D36M-14(2020) and normally held at or above 105 °C for elastomeric binder systems. Low-temperature flexibility is evaluated by EN 1109, while elastic recovery is assessed under ASTM D6084/D6084M-21 with a target of ≥80% for torch-applied membranes. The addition ratio is process-critical: below 8 wt% T-413, crack resistance at low temperature declines and elastic recovery falls below specification; above 14 wt%, binder viscosity approaches the upper limit of practical membrane coating unless aromatic process hydrocarbon or softer base bitumen is introduced. The downstream process line applies the hot polymer-modified bitumen onto polyester or glass-fiber reinforcement, followed by sanding or polyethylene film lamination. Terminal products are torch-applied and self-adhered SBS-modified bitumen waterproofing sheets used in built-up roof assemblies, below-grade waterproofing, and bridge deck membranes. Storage-stability testing after 24 h at 180 °C must show a softening point differential no greater than 5 °C between top and bottom thirds according to EN 13399; separation beyond this limit indicates insufficient shear, polymer feed variation above ±0.5 wt%, or bitumen chemistry incompatibility.
| Standard designation | Property evaluated | Industrial acceptance boundary |
|---|---|---|
| EN 13707:2004+A2:2009 | Flexible sheet product family | Polymer-modified bitumen sheeting |
| ASTM D6164/D6164M-21 | SBS-modified sheet performance | Pass flexibility at -10 °C |
| ASTM D36/D36M-14(2020) | Softening point | ≥ 105 °C |
| ASTM D6084/D6084M-21 | Elastic recovery | ≥ 80% |
| EN 1109 | Low-temperature flexibility | No cracking at -10 °C |
| EN 13399 | Storage stability after 24 h at 180 °C | Softening point differential ≤ 5 °C |
Prior to compounding, SBS T-413 granules are tumble-blended with naphthenic oil at 15–25 wt%, general-purpose polystyrene at 10–20 wt%, and calcium carbonate filler at 10–25 wt%; SBS T-413 itself is charged at 30–45 wt% of the total compound. The compound is processed on a 36:1 L/D co-rotating twin-screw extruder with barrel temperatures 150/160/170/180/175 °C, strand-pelletized, and dried to <0.1% moisture before injection molding; if ambient relative humidity exceeds 60%, pre-drying at 70 °C for 2 h is required to prevent porosity and surface streaks. Injection molding is performed at melt temperatures of 160–190 °C and injection pressures of 60–100 MPa, with mold temperature controlled at 20–40 °C to preserve the styrene domain network and reduce post-molding shrinkage anisotropy. Footwear compliance is governed by REACH EC 1907/2006; abrasion is tested under ISO 20871 and hardness under ISO 868, while safety footwear adds EN ISO 20345:2011 requirements for slip resistance and energy absorption. A production bottleneck occurs during cavity filling when injection speed exceeds 60 cm³/s or gate shear rate surpasses 10,000 s⁻¹; the resulting strain-induced orientation of the styrene phase produces flow marks and tensile strength loss after demolding. Terminal components are casual footwear unit soles, slipper soles, and low-profile TPR midsoles substituting vulcanized rubber. Published data for T-413-specific Ross flex cut growth in footwear compounds is limited; validation screening should therefore use ASTM D1052-09(2019) or equivalent flex testing against a qualified control compound.
For solvent-borne contact adhesives used in furniture edge banding and footwear upper assembly, SBS T-413 is dissolved at 12–20 wt% solids in a toluene/acetone/n-hexane solvent blend, where the low-boiling fraction is 60–80%; rosin ester or alkylphenol tackifier is added at 5–8 wt% on total solution to raise room-temperature grab. The relevant regulatory boundary is REACH EC 1907/2006 for solvent and residual monomer content, while bond strength is measured by ASTM D816 for contact adhesives or ISO 4587:2003 for lap shear. Manufacturing uses a high-speed dissolver at 500–800 rpm to limit polymer chain degradation during dissolution, followed by roller or gravure coating at 80–120 g/m² dry coating weight and drying tunnel temperatures of 60–70 °C. Terminal products include leather-to-rubber lamination adhesives for footwear upper assembly, melamine edgebanding adhesives, and foam-to-fabric laminating adhesives. Pot viscosity is checked with ASTM D2196-20 at 25 °C; drift beyond ±15% signals solvent evaporation or oxidative attack, and the solution should not remain in unsealed vessels for more than 8 h at ambient temperature.
At asphalt mixing plants, SBS T-413 is fed into penetration-grade bitumen at 3.5–6.0 wt% of binder mass and dispersed through an inline high-shear mill at 175–185 °C; rotational speed is maintained at 3,500–5,000 rpm with a recirculation rate passing the entire tank volume through the mill every 10–15 min. The resulting polymer-modified binder is specified under EN 14023:2010 for polymer-modified bitumen and AASHTO M 320 performance grading, with elastic recovery measured by ASTM D6084/D6084M-21 or EN 13398 and normally maintained above 70% at 3.5 wt% polymer addition. The dominant process conflict is storage stability: after 72 h at 180 °C, the softening point difference between top and bottom samples must not exceed 5 °C under EN 13399. Insufficient shear time below 60 min or a temperature drop below 170 °C creates dispersed polymer domains that coalesce during storage and fail separation testing. Terminal product types include heavy-duty road surface course binders, airport runway overlays, and bridge deck asphalt binders requiring simultaneous high-temperature rutting resistance and low-temperature crack resistance. Operational boundaries include avoidance of highly paraffinic bitumen grades and sustained temperatures above 200 °C to prevent SBS chain scission; field data from fixed-silo mixing lines show that viscosity-based feedback control stabilizes batch-to-batch elastic recovery within ±3%.
Thermoplastic elastomer compounds based on SBS T-413 for overmolded grips are processed on 36:1 L/D co-rotating twin-screw extruders with T-413 charged at 35–50 wt%, white mineral oil at 15–25 wt%, polypropylene at 10–20 wt%, and inorganic filler at 5–15 wt%; pellets are dried below 0.1% moisture prior to overmolding. Compliance is anchored to RoHS Directive 2011/65/EU, REACH EC 1907/2006, and EN 71-3:2019+A1:2021 when the finished grip or toy handle enters the European toy market. The overmolding process uses a two-shot injection molding cell with barrel temperatures 170–200 °C, mold temperatures 25–45 °C, and clamp force sufficient for 250–400 t presses; polypropylene substrates are used directly, while polyethylene substrates require corona pre-treatment. Hardness is measured by ISO 868 after 24 h conditioning, and tensile properties by ISO 527-2:2012; hardness drift after post-molding annealing at 70 °C for 2 h should remain below 3 Shore A, or oil extension must be reduced to prevent surface exudation. Terminal product types include screwdriver grips, power tool soft-touch overmolds, toothbrush handles, and child-use toy grips. Published data for T-413-specific compression set after overmolding is limited; validation therefore uses ISO 815-1:2019 with a control grade and a defined annealing protocol rather than relying solely on supplier datasheet values.
Competitive Asahi Kasei Asaprene™ SBS T-413 prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please contact us at +8618005193850 or mail to sales8@ascent-chem.com.
We will respond to you as soon as possible.
Tel: +8618005193850
Email: sales8@ascent-chem.com
Flexible payment, competitive price, premium service - Inquire now!
Asahi Kasei Asaprene™ T-413 is a linear styrene-butadiene-styrene triblock copolymer produced by anionic polymerization. The pellet is supplied without paraffinic oil extension, and lot certificates of analysis report a styrene content of 30 wt% with a butadiene content of 70 wt%. The terminal polystyrene blocks form a physical-crosslink network below the styrenic glass transition near 95 °C, while the unsaturated polybutadiene midblock contributes elongation, tack formation, and energy absorption above its glass transition near -80 °C. This two-phase morphology permits repeated thermoplastic processing without sulfur or peroxide vulcanization, but the unsaturated midblock remains sensitive to oxygen, ozone, and shear-induced chain scission. The unextended nature of T-413 keeps the as-supplied density near 0.94 g cm⁻³ under ASTM D792, and injection-molded specimens typically show a Shore A hardness of 78 under ASTM D2240-15 and a tensile stress at break near 18.0 MPa under ASTM D638-14.
The property set commonly used to differentiate T-413 from other SBS block copolymers is summarized in Table 1. The values are typical lot averages from manufacturer technical data and should not be read as guaranteed release limits. Where a test designation is absent from a certificate of analysis, the laboratory responsible for release testing must be identified before the data are used for design qualification.
| Property | Typical value | Test method |
|---|---|---|
| Styrene content | 30 wt% | manufacturer QA / NMR |
| Specific gravity | 0.94 g cm⁻³ | ASTM D792 |
| Tensile strength at break | 18.0 MPa | ASTM D638-14 |
| Elongation at break | 700% | ASTM D638-14 |
| Hardness | 78 Shore A | ASTM D2240-15 |
| Modulus at 300% elongation | 1.5 MPa | ASTM D412-16 |
The 30 wt% styrene content places T-413 in the low-styrene SBS class. The hard-phase volume fraction is sufficient to reduce cold flow under ordinary storage, but low enough to retain tack development in formulated adhesive systems. Because the polybutadiene midblock is unsaturated, storage in direct sunlight or near strong oxidizing agents must be avoided; ozone attack can generate a crosslinked pellet surface that appears as gel specks in extruded profiles.
Melt-state processing of T-413 is normally performed on corotating twin-screw extruders with 36:1–48:1 L/D ratios and segmented mixing elements. Feed-zone temperatures are maintained at 120–140 °C, plastication zones are managed below 190 °C, and the die head is held between 180 °C and 200 °C depending on throughput. High-shear kneading blocks should not be concentrated in a single barrel section because the polybutadiene phase undergoes shear-induced chain scission; distributive mixing elements are preferred. Residence time at melt temperature should not exceed 2–4 minutes on a 44:1 L/D corotating twin-screw extruder. On production-scale lines, screw speed is often limited to 250–350 rpm. Higher screw speeds can generate melt temperatures above 220 °C, at which oxidative degradation forms carbonyl species detectable by FTIR near 1720 cm⁻¹. Degraded material typically shows reduced elongation at break and increased melt flow rate; post-extrusion lot testing by ASTM D638-14 is therefore used as a process-control tool rather than as a sole release criterion.
Injection molding of neat T-413 uses a general-purpose screw with a compression ratio of 2.5:1–3.0:1, a barrel profile of 160–200 °C, and a mold temperature between 20 °C and 45 °C. Molded plaques of 2.0 mm thickness are conditioned at 23 ± 2 °C and 50 ± 5 % relative humidity for 24 h before testing per ASTM D638-14. Failure to condition specimens can produce hardness and modulus drift. On injection lines, insufficient clamp force or low packing pressure magnifies sink marks at rib intersections; published data for T-413 in this exact equipment configuration is limited, but the failure pattern is consistent with high melt viscosity and rapid solidification of the polystyrene end-blocks.
In polymer-modified bitumen, T-413 is typically compounded at 3–6 wt% into paving-grade bitumen using a high-shear rotor-stator mill or a twin-screw extruder. Mixing temperature is held between 170 °C and 190 °C, and rotor-stator shear rates are commonly above 10,000 s⁻¹. At this temperature, the polystyrene domains soften and the polybutadiene midblock swells with the maltene phase; the resulting binder is a biphasic dispersion rather than a molecular solution. Storage stability of the modified binder is assessed by EN 13399, softening point by ASTM D36, elastic recovery by ASTM D6084, and dynamic shear rheology by AASHTO T 315. A typical SBS modification raises the high-temperature performance grade of a 60/70 pen base bitumen, but full grading of T-413 in a specific binder must be confirmed by AASHTO M 332. Published data for T-413 in this exact binder configuration is limited.
Phase separation of a polymer-rich top layer in vertical storage tanks is the primary large-scale failure mode. Sulfur or peroxide crosslinking at 0.1–0.3 wt% based on bitumen weight is sometimes used to create a three-dimensional network, but overdosing raises viscosity beyond pumpable limits at 135 °C. Field-scale trials use a Brookfield thermosel viscometer with an SC4-27 spindle at 135 °C to verify that viscosity remains below 3000 mPa·s before tank transfer; this limit is an equipment constraint rather than a material specification.
Hot-melt pressure-sensitive adhesive formulations based on T-413 are prepared by compounding the block copolymer with C5 aliphatic tackifying resins and naphthenic process oils. A starting formulation near 100 phr T-413, 80–120 phr tackifier, and 20–40 phr process oil is evaluated, but the optimum depends on tackifier softening point and oil aromaticity. Peel adhesion is measured under ASTM D3330/D3330M using a 180° peel angle on stainless steel after 24 h dwell; loop tack is measured under ASTM D6195; and shear adhesion failure temperature is measured under ASTM D4498 with a 500 g static load. Because T-413 has high molecular weight, insufficient oil exudation can lower peel force and shift failure mode from interfacial debonding to cohesive failure; the test record must include failure-mode designation under ASTM D3330/D3330M rather than peel force alone.
In footwear, T-413 is injection-molded or extruded into unit soles and midsoles after blending with polystyrene and process oil. The low styrene content reduces room-temperature stiffness and supports the flexibility characteristic of shoe-sole applications. Slip resistance is evaluated by ASTM F2913-19 or ISO 13287:2019, and abrasion resistance by DIN 53516. The absence of ester plasticizers in the base polymer reduces migration risk toward adhesives and upper materials, but formulated compounds must still be checked for plasticizer exudation after accelerated aging.
Within the SBS product class, T-413 is positioned as an unextended low-styrene triblock. Compared with oil-extended SBS, T-413 contains no paraffinic oil in the pellet; the as-supplied density remains near 0.94 g cm⁻³, and the compounder retains control over oil type and loading. Compared with higher-styrene SBS containing 40–45 wt% styrene, T-413 exhibits lower Shore A hardness and a lower room-temperature storage modulus because the polystyrene hard phase occupies a smaller volume fraction. The trade-off is a reduction in maximum service temperature and a greater tendency to cold flow under uncompressed storage. In adhesive systems, the lower styrene content usually yields higher tack at equivalent tackifier loading but lower shear holding power as measured by ASTM D4498.
| Comparison axis | T-413 | Oil-extended SBS | Higher-styrene SBS |
|---|---|---|---|
| Styrene content | 30 wt% | 30–33 wt% plus oil | 40–45 wt% |
| Shore A hardness after molding | 78 Shore A | lower after oil dilution | 85–90 Shore A |
| Melt viscosity | high; no oil reduction | reduced by oil | elevated hard-phase viscosity |
| Tack development in adhesives | moderate | high | lower |
| Service temperature ceiling | low-to-moderate | reduced by oil | higher |
As a modifier for general-purpose polystyrene, T-413 is melt blended at 5–20 wt%. The polystyrene end-blocks provide intrinsic compatibility with the polystyrene matrix, and notched Izod impact energy measured on 3.18 mm specimens under ASTM D256-10 can be raised while tensile modulus declines. Compounds must include adequate antioxidant stabilization because the unsaturated midblock degrades under repeated heat histories.
Regulatory documentation for the polymer should be obtained from the supplier before use in food-contact articles. The generic material is not sold as a direct food-contact polymer; article-specific migration testing under FDA 21 CFR or applicable European regulations is required for any formulation intended for such use. Under REACH and RoHS 2011/65/EU, compliance declarations must be confirmed against the exact commercial lot because additive packages and third-party modifiers can alter the final article classification.