| HS Code | 936524 |
| Product Name | Asahi Kasei Asaprene™ SBS T-437L |
| Polymer Type | Styrene-butadiene-styrene (SBS) block copolymer |
| Block Structure | Linear triblock |
| Styrene Content | 30 wt% |
| Butadiene Content | 70 wt% |
| Appearance | White to off-white pellets or crumb |
| Density | 0.94 g/cm³ |
| Melt Flow Rate | 1.5 g/10 min (200°C, 5 kg) |
| Shore A Hardness | 70 |
| Tensile Strength | 20 MPa |
| Elongation At Break | 800% |
| Solution Viscosity | 1,200 mPa·s (25 wt% in toluene, 25°C) |
| Volatile Matter | ≤1.0 wt% |
| Ash Content | ≤0.2 wt% |
As an accredited Asahi Kasei Asaprene™ SBS T-437L factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Asahi Kasei Asaprene™ SBS T-437L is supplied in 25 kg net paper bags, typically 40 bags (1,000 kg) per pallet. |
| Container Loading (20′ FCL) | Asahi Kasei Asaprene™ SBS T-437L loaded in a 20-foot FCL container, securely palletized and shipped under standard chemical cargo conditions. |
| Shipping | Asahi Kasei Asaprene™ SBS T-437L is shipped as non-hazardous polymer pellets, typically in 25 kg bags or 1,000 kg jumbo bags on pallets in dry containers. Keep dry, cool, and away from direct sunlight; no UN transport classification applies. |
| Storage | Store in a cool, dry, well-ventilated area away from direct sunlight, heat, flames, and oxidizing agents. Keep containers tightly closed and protect from moisture, contamination, and physical damage. Avoid prolonged exposure to high temperatures. Use first-in, first-out stock rotation, maintain clear labeling, and follow the manufacturer’s SDS and local regulations. Do not store near food, feed, or incompatible chemicals. |
| Shelf Life | Typically 24 months from production when stored in original unopened packaging in a cool, dry, dark place. |
Polymer-modified bitumen production using Asaprene T-437L is conducted in a high-shear rotor-stator mill rather than a low-speed paddle mixer because solution-grade SBS particles must be comminuted and swollen simultaneously. A typical binder formulation targets 3–7 wt% polymer based on bitumen mass; below 3 wt% the swollen styrene network is discontinuous and high-temperature rutting resistance under AASHTO T350-22 may fall below traffic-grade thresholds, while above 7 wt% the binder can reach a mixing viscosity that exceeds the feed capacity of many road-tanker pumps without heating jackets. Asaprene T-437L is added to penetration-grade bitumen preheated to 180–190°C; the mill tip speed is maintained between 15 and 25 m/s until no visible polymer gel specks remain in a drawdown film. Crosslinking with elemental sulfur at 0.05–0.15 wt% of bitumen mass is sometimes introduced to suppress phase separation during hot storage; this requires strict temperature control because sulfur-vulcanized SBS networks lose stability above 200°C. PMB specifications under EN 14023:2010 require a softening point by EN 1427 typically above 70°C, elastic recovery by EN 13398 above 80%, and storage stability by EN 13399 with a softening-point difference below 5°C after 72 h at 180°C. In emulsified asphalt or cold-mix variants, the same SBS grade must be pre-compounded because direct latex addition does not form the same styrene-domain connectivity. Published data for T-437L in chemically crosslinked warm-mix asphalt at lower temperatures is limited.
| Control parameter | Standard | Typical PMB threshold |
|---|---|---|
| Softening point | EN 1427 | ≥70°C |
| Elastic recovery at 25°C | EN 13398 | ≥80% |
| Storage stability ΔR&B | EN 13399 | ≤5°C |
| Dynamic shear rutting factor | ASTM D7175-23 | ≥1.0 kPa at 10 rad/s |
In hot-melt pressure-sensitive adhesive compounding, Asaprene T-437L is combined with tackifying resins and plasticizers in a jacketed sigma-blade mixer at 150–170°C under a nitrogen blanket. A starting formulation contains 100 phr T-437L, 80–120 phr hydrogenated C5 aliphatic resin, 40–60 phr naphthenic process oil, and 1 phr hindered phenolic antioxidant. The melt is discharged through a heated extruder or gear pump to a slot-die coater; coat weight for paper labels is controlled at 20–30 g/m². Loop tack measured by ASTM D3654/D3654M-06 and 180° peel adhesion by ASTM D3330/D3330M-04 depend on the resin aromatic/aliphatic balance: excessive aromatic content selectively swells the styrene end-blocks, lowering shear adhesion failure temperature determined by ASTM D4498-07. Production-scale adhesive lines typically show die-lip build-up from low-molecular-weight diblock fractions when the die temperature is not held 5–10°C above melt temperature; a 200-mesh breaker plate is installed to reduce transfer of degraded gel particles to the coating head. Because T-437L contains unsaturated butadiene midblocks, hot-melt tanks should not be held at 170°C for more than 8 h without nitrogen purge; oxidative chain scission generates tack drift that cannot be corrected by additional tackifier. For packaging tapes, lower tackifier loading near 80 phr is used to retain cohesive strength, while removable labels use higher oil loading up to 80 phr to reduce peel force without phase separation.
Injection molding of microcellular footwear soling compounds based on Asaprene T-437L uses a formulation in which the SBS elastomer is blended with general-purpose polystyrene as a flow modifier and hardness builder. A representative soling compound contains 100 phr T-437L, 30–50 phr crystal polystyrene, 10–25 phr precipitated calcium carbonate, 10–20 phr naphthenic oil, 0.5–1.0 phr azodicarbonamide blowing agent, and 0.3–0.5 phr antioxidant. The compound is pelletized on a co-rotating twin-screw extruder with L/D 36:1 at barrel temperatures of 150–175°C, then injection molded on a reciprocating-screw machine with barrel temperatures of 160–190°C and mold temperatures between 25°C and 40°C. Gas evolution from azodicarbonamide begins near 160°C; therefore the shot size should not exceed 60–70% of maximum injection volume to allow frothed melt expansion into the cavity without excessive clamp pressure. If the mold parting line is inadequately vented, decomposition gas produces surface burn marks and trapped voids at the thickest sole cross-section. Final sole density is controlled between 0.55 and 0.85 g/cm³; abrasion loss measured by ISO 4649:2017 method A is generally below 250 mm³ in well-fused skins, and flex-cut growth resistance is evaluated according to DIN 53543 at 50,000 cycles without significant crack penetration. Published formulation-specific data for T-437L in azodicarbonamide-foamed soling is limited; the processing window above is based on standard linear SBS soling compounds of similar bound styrene content.
Solvent-borne construction sealants prepared with Asaprene T-437L require a low-aromatic aliphatic solvent blend because aromatic solvents reduce final cohesive strength by partially dissolving the styrene domains. A production batch is mixed at 40–60 rpm in a planetary dissolver until the SBS is fully swollen; target solids content is 55–70 wt%. A representative formulation includes 100 phr T-437L, 60–90 phr aliphatic hydrocarbon resin, 50–80 phr treated ground calcium carbonate, 30–50 phr plasticizer, and 1 phr wetting agent. The finished sealant is tested for slump by ASTM D2202 at ≤1 mm, for tensile behavior by ASTM D412, and for joint movement capability under EN 15651-1 or ASTM C920. The low-viscosity character of T-437L permits filler loading up to 35–40 wt% without exceeding trowel-grade rheology; however, addition of more than 10 phr of a highly aromatic process oil should be avoided because it accelerates tackifier migration to concrete and glass substrates after outdoor exposure. On façade production lines, adhesion to anodized aluminum and concrete after water immersion is evaluated by ASTM C794. Batch-to-batch variation in thixotropy is controlled by the ratio of treated filler to resin: increasing filler above 80 phr lowers slump but also reduces extensibility during joint movement.
| Property | Standard | Typical control threshold |
|---|---|---|
| Slump | ASTM D2202 | ≤1 mm |
| Tensile strength | ASTM D412 | ≥0.7 MPa |
| Joint movement capability | EN 15651-1 | ≥25% |
| Adhesion-in-peel after immersion | ASTM C794 | No cohesive failure |
A co-rotating twin-screw extruder with L/D 44:1 can compound Asaprene T-437L into filled thermoplastic elastomer pellets used for automotive mats, extruded edge trims, and flexible appliance parts. The SBS is fed through the main hopper with a gravimetric feeder, while polypropylene homopolymer and filler are introduced downstream through a side-stuffer after the SBS has been fused. Barrel temperatures are set according to a flat profile of 160–180°C; the die head is held at 170°C to avoid strand melt fracture. A representative formulation contains 100 phr T-437L, 30–50 phr polypropylene homopolymer with melt flow index 25–35 g/10 min measured at 230°C/2.16 kg under ISO 1133-1:2022, 20–40 phr talc or calcium carbonate, and 20–40 phr white mineral oil. Output on a 75 mm twin-screw line is limited by pelletizing water temperature: if the water bath is below 25°C, strands become brittle and fracture during pelletization, generating fine particles that later cause melt-filter plugging; above 40°C, pellets agglomerate in the centrifuge dryer. Mechanical testing after injection molding includes tensile strength and elongation by ISO 527-2:2012, hardness by ISO 868 at Shore A 60–75, and compression set by ISO 815-1:2019 at 70°C for 24 h, with reported values generally below 55% for unfilled SBS/PP blends. Published grade-specific compression set data for T-437L at filler loadings above 40 phr is limited.
Continuous extrusion of Asaprene T-437L into gasket profiles and flexible sheet is performed on a single-screw extruder with a barrier screw length-to-diameter ratio of 30:1. The feed throat is cooled to 15–20°C; otherwise pellets soften prematurely and bridge over the feed opening. A typical gasket formulation uses 100 phr T-437L, 20–40 phr precipitated silica or hard clay, 15–30 phr naphthenic oil, 1–2 phr stearic acid, 0.5–1 phr antioxidant, and 0.2–0.5 phr processing lubricant. The die temperature is set 5–10°C lower than the last barrel zone to increase melt viscosity and prevent swell-induced dimensional variation. Extrudate surface quality is evaluated against a profile tolerance of ±0.2 mm for automotive weatherstrip and ±0.5 mm for general gasket profiles. Because the butadiene midblock is unsaturated, compounds based on T-437L are not recommended for continuous service above 70°C in air without an antioxidant system; in enclosed gasket applications above 90°C, EPDM or SEBS should be substituted. Compression set tested by ISO 815-1:2019 at 70°C for 24 h is controlled more by filler loading than by oil loading; high filler levels above 40 phr increase hardness but also increase compression set and reduce tear strength.
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Asahi Kasei Asaprene™ SBS T-437L is a linear styrene-butadiene-styrene thermoplastic elastomer supplied in pellet form for injection moulding, extrusion, and compounding. The product is positioned as a low-hardness, high-flow grade in the Asaprene SBS portfolio. The polybutadiene midblock forms a continuous elastomeric phase at service temperature, while the styrene endblocks aggregate into discrete domains that act as physical crosslinks, permitting melt reprocessing without sulphur vulcanization. Publicly available manufacturer data indicate a bound styrene content of approximately 30 wt%, a specific gravity of 0.94 under ASTM D792, and a Shore A hardness in the 45–55 range. The datasheet property envelope places tensile strength at 10–14 MPa and elongation at break above 600% under ASTM D638.
The difference is controlled by styrene endblock association and the order-disorder transition temperature. In T-437L, the bound styrene content is lower than in 38–45 wt% styrene grades, so the phase-separated styrene network relaxes at a lower temperature. The result is a melt flow rate in the 8–15 g/10 min range at 190°C and 2.16 kg under ISO 1133-1:2022, compared with 2–5 g/10 min for a higher-styrene SBS of similar molecular weight. The linear architecture further reduces melt elasticity and die swell relative to radial SBS, which is advantageous in low-pressure mould filling but reduces melt strength in free-extrusion operations.
Compounding with T-437L follows the standard shear-history sequence for unsaturated styrenic block copolymers. A pre-drying step is not mandatory because the polymer is not hygroscopic, but surface condensation on cold pellets stored below dew point can generate cosmetic splay. When hopper drying is used, a 70°C dehumidified-air condition for 2 h is sufficient. The recommended melt-temperature window is 150–180°C for injection moulding and 150–170°C for extrusion, with residence time kept below 10 min on a single-screw extruder with 24:1 L/D. At melt temperatures above 210°C, thermo-oxidative chain scission of the unsaturated midblock becomes measurable as a loss of tensile strength and an increase in gel defects.
Short-shot defects in thin-wall grips and infant-care overmoulds are controlled by the temperature window and gate shear history. T-437L is processed in reciprocating screw machines with screw L/D ratio between 20:1 and 24:1, compression ratio from 2.2:1 to 2.8:1, and a non-return valve of sufficient annular flow area to avoid stagnation. Mould temperatures between 20°C and 40°C permit ejection without surface tack; lower mould temperatures shorten cycle time but can increase orientation shrinkage near the gate. Gate geometry should maintain shear rates below 100,000 s⁻¹. Above this threshold, frictional temperature rise of 20°C or more can initiate chain scission and gate blush. Injection velocity is typically set at 30–70 mm/s for thin-walled parts; high velocity reduces melt viscosity but raises shear heating, so the lower end of this range is used for sprues with small diameters.
Addition of paraffinic or naphthenic oil at 5–30 phr lowers compound hardness but increases surface exudation risk when the oil loading exceeds the solubility limit of the polybutadiene midblock. Aromatic oils are not recommended because they partition into the styrene domains and reduce tensile strength and creep resistance. The stabilizer package should include a hindered phenolic antioxidant at 0.1–0.3 phr and a phosphite secondary antioxidant at 0.1–0.2 phr; sulphur-based synergists can generate odour in skin-contact applications and are generally avoided. For white compounds, titanium dioxide at 2–5 phr increases opacity but raises melt viscosity and may require a 5–10°C increase in barrel temperature within the 180°C ceiling. Zinc stearate as a mould-release aid should be kept below 0.5 phr to limit plate-out on tool surfaces at elevated mould temperatures.
Lot-specific values should be taken from the certificate of analysis; the following envelope reflects the public datasheet category and is not a contractual specification.
| Property | Typical datasheet envelope | Test method |
|---|---|---|
| Hardness | 45–55 Shore A | ASTM D2240 |
| Tensile strength | 10–14 MPa | ASTM D638 |
| Elongation at break | 600–750% | ASTM D638 |
| Specific gravity | 0.93–0.95 | ASTM D792 |
| Melt flow rate at 190°C/2.16 kg | 8–15 g/10 min | ISO 1133-1:2022 |
| Bound styrene | 28–32 wt% | ASTM D5775 |
Footwear unit soles are compounded to a hardness of 35–55 Shore A; T-437L provides sufficient flow to fill the toe-spring radius without increasing injection pressure above 800 bar. In soft-touch overmoulding onto polypropylene substrates, adhesion is improved when the substrate surface temperature exceeds 70°C or when a styrene-ethylene-butylene-styrene tie layer is used. Impact-modification of general-purpose polystyrene at 5–20 wt% raises ductility, but published data for this specific grade in that compound is limited; formulation-specific Izod impact testing is required under ASTM D256.
The midblock unsaturation makes T-437L inherently less resistant to oxidative embrittlement than hydrogenated SEBS. Outdoor service life without carbon black or hindered amine light stabilizers is limited because ultraviolet radiation cleaves the polybutadiene chain and crosslinks the rubber phase. Carbon black at 2 wt% or a hindered amine light stabilizer at 0.2–0.5 phr is required for weatherable compounds. Ozone exposure induces surface cracking under strain; antiozonant waxes are only partially effective because the thermoplastic process disperses the wax but does not cure it into a continuous protective film. The maximum continuous service temperature in air is generally 70°C for unreinforced compounds; above this temperature, the polystyrene domains soften and creep becomes measurable.
Regulatory status is formulation-dependent. The base polymer is subject to the monomer registration and information requirements of REACH EC 1907/2006. Restriction of hazardous substances compliance under RoHS 2011/65/EU requires verification that the compounded article does not exceed the maximum concentration values for lead, cadmium, mercury, hexavalent chromium, PBB, and PBDE. Food-contact suitability is not automatically conferred by the base resin; migration testing under EU 10/2011 or end-use compliance with 21 CFR 177.1810 is required for the finished article. Plasticizer and antioxidant selections must be appropriate for the legal region and application.
| Standard or regulation | Relevant scope | Application requirement |
|---|---|---|
| REACH EC 1907/2006 | Substance registration and SVHC communication | Verify monomer and additive registration for EU market |
| RoHS 2011/65/EU | Homogeneous material limits for Pb, Cd, Hg, Cr(VI), PBB, PBDE | Electrical and electronic equipment |
| EU 10/2011 | Plastic food-contact migration | Food-contact articles require migration modelling or testing |
| 21 CFR 177.1810 | Styrene block copolymers in food-contact elastomers | Finished rubber article must meet end-use extraction limitations |
Styrenic block copolymers are used in paving-grade bitumen at 2–5 wt% to raise rutting resistance and elastic recovery. T-437L’s lower styrene content tends to reduce mixing viscosity compared with 30–40 wt% styrene SBS, but may also reduce high-temperature storage stability of the modified binder. Published data for T-437L in bitumen blend storage stability is limited; laboratory trials are required to determine phase separation under ASTM D7173 and performance grade under AASHTO M320.
Reprocessing of edge trim and sprues can be performed at 10–20 wt% in non-appearance applications, but the shear history reduces elongation at break by approximately 5–10% relative to virgin material under ASTM D638. Re-grind must be free of polyolefin contamination because polyethylene and polypropylene phase-separate at the interface and reduce weld-line strength. Batch-to-batch melt flow rate variation of ±1.5 g/10 min may require minor adjustment of hold pressure or cushion to maintain part mass.