| HS Code | 729274 |
| Appearance | White to off-white powder |
| Polymer Type | Styrene-butadiene-styrene (SBS) block copolymer |
| Form | Powder |
| Styrene Content | 40 wt% |
| Density | 0.98 g/cm³ |
| Melt Flow Rate | 0.5 g/10 min (200°C, 5 kg) |
| Shore A Hardness | 90 |
| Tensile Strength | 20 MPa |
| Elongation At Break | 700% |
| 300 Percent Modulus | 5 MPa |
| Tear Strength | 35 kN/m |
| Vicat Softening Point | 65°C |
| Volume Resistivity | >10^15 Ω·cm |
| Water Absorption | <0.1% |
As an accredited Asahi Kasei Asaprene™ SBS T-420P factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Asahi Kasei Asaprene™ SBS T-420P is supplied in 25 kg moisture-resistant paper bags, typically 40 bags (1,000 kg) per pallet. |
| Container Loading (20′ FCL) | 20′ FCL container loaded with Asahi Kasei Asaprene™ SBS T-420P, securely palletized, dry-stowed, labeled, and compliant for transport. |
| Shipping | Asahi Kasei Asaprene™ SBS T-420P is shipped as solid styrene-butadiene-styrene block copolymer pellets in moisture-resistant bags or boxes. It is generally non-hazardous for transport, requires dry ambient storage, and should be kept away from excessive heat, sunlight, and moisture. Standard industrial handling precautions apply; consult the SDS and local regulations. |
| Storage | Store in a cool, dry, well-ventilated area away from direct sunlight, heat, sparks, and flames. Keep containers tightly closed to prevent moisture and contamination. Avoid prolonged exposure to UV light and ozone. Maintain moderate, stable temperatures; do not stack in a way that causes deformation. Follow local regulations and the safety data sheet. |
| Shelf Life | Typically 24 months from production when stored unopened in a cool, dry place, away from direct sunlight and heat. |
Hot mixing Asaprene T-420P into styrenic-rich injection molding compounds for footwear shells normally starts with a dry blend of 100 phr T-420P, 10–35 phr crystal polystyrene, 30–70 phr paraffinic or naphthenic extender oil, and 10–25 phr precipitated calcium carbonate. The dry blend is mixed in a high-speed mixer at 80–110 °C until oil uptake is visually uniform, then fed to a co-rotating twin-screw extruder with an L/D ratio of 40:1 and a melt temperature of 170–190 °C. On production lines with screw speeds above 400 r/min, excessive shear heating can push the melt above 220 °C, producing edge tackiness, gel bodies at the die lip, and batch-to-batch Shore A variation. The compound is typically pelletized through a strand bath with die-face temperatures kept below 35 °C to prevent strand fusion. Shore A hardness is adjusted between 55 and 75 by oil loading; higher crystal polystyrene content raises stiffness but reduces flex crack resistance under repeated bending. ASTM D2240-15e1 hardness and ASTM D624 die C tear strength are used for lot release, with tear strength generally remaining above 25 N/mm when oil loading is held below 80 phr. DIN 53516 abrasion volume loss usually stays below 200 mm³ when calcium carbonate does not exceed 25 phr. Pre-drying at 60–70 °C for 2 h is required when ambient relative humidity exceeds 60% or when hygroscopic fillers are incorporated. Injection molding is carried out on machines with 800–1600 kN clamp force using general-purpose screws with 20:1 to 22:1 L/D, medium injection speeds of 30–60 mm/s, and back pressure of 3–8 bar. Gate freeze-off at sub-2 mm wall sections can cause sink marks if holding pressure drops below 40 bar before the gate seals; venting depth should not exceed 0.02 mm to avoid flash in low-viscosity formulations.
| 100 phr Asaprene T-420P | Crystal polystyrene 10–35 phr | Paraffinic/naphthenic oil 30–70 phr | Calcium carbonate 10–25 phr | Antioxidant 0.2–0.5 phr |
| ASTM D2240-15e1 | ASTM D624 | DIN 53516 | ASTM D395-16e1 | ISO 1133-1:2022 |
In oxidized bitumen waterproofing membranes, Asaprene T-420P is dispersed into bitumen at 180–195 °C using a high-shear homogenizer or rotor-stator mill. The dosage window of 10–14 wt% is critical because below 10 wt% the polybutadiene midblocks cannot form a continuous network, and low-temperature flexibility under EN 1109 drops sharply. The mixing sequence affects phase morphology: bitumen is first heated to 180 °C in a jacketed vessel, then T-420P pellets are added under slow agitation at 300–500 r/min. After polymer softening, shear is increased to 3000–5000 r/min for 60–120 min. At mixing temperatures below 175 °C, unswollen SBS domains remain as discrete elastic islands, causing separation during storage and uneven film thickness in calendering. At temperatures above 205 °C, oxidative degradation of the polybutadiene segments raises the melt viscosity and produces a grainy surface. The modified binder is stabilized with 0.2–0.5 wt% hindered phenolic antioxidant and processed through a three-roll calender at 140–160 °C onto polyester or glass-fiber carriers. Finished membranes are tested according to ASTM D5147 for thickness, tensile elongation, and water resistance, while low-temperature flexibility is checked at -10 °C or -20 °C under EN 1109. Production-scale failure modes include fisheyes when undispersed polymer pellets survive the high-shear step, and pinholes when moisture is present in the filler or carrier at calendering. Mineral filler such as talc or limestone is limited to 15–30 wt% because higher filler loading increases viscosity and masks the elastic recovery of SBS domains. Published data for this specific grade in oxidized bitumen membrane systems is limited, but the processing boundaries described are consistent with industrial SBS-modified bitumen practice.
Pressure-sensitive adhesive hot melts based on Asaprene T-420P are compounded with C5 aliphatic hydrocarbon tackifier resins at 70–120 phr and a naphthenic or white mineral oil at 10–30 phr. The polymer is first masticated in a sigma-blade mixer at 140–150 °C, then tackifier is added after the polymer melt becomes clear. Oil is added last to prevent slippage and phase inversion. Coating is performed through a slot die at 130–160 °C onto silicone-coated release liner, with coat weights of 20–40 g/m² for label and tape applications. Because SBS T-420P contains polystyrene endblocks, the melt viscosity remains fairly high at low shear, and die-lip build-up occurs if the adhesive is held at coating temperature for more than 8 h without nitrogen blanketing. Formulators select tackifiers with softening points below 110 °C to maintain clarity; high softening point C9 resins above 130 °C can produce haze and reduce peel adhesion. ASTM D3330/D3330M peel adhesion on stainless steel is typically evaluated at 180° peel angle and a dwell time of 20 min. Loop tack under ASTM D6195 is more sensitive to oil migration than peel adhesion, so oil content is normally kept below 25 phr. The amorphous polybutadiene midblock provides low-temperature flexibility, but ultraviolet exposure causes discoloration and surface deadening unless hindered amine light stabilizers are added at 0.1–0.3 wt%. Antioxidant loading of 0.3–0.5 wt% is used to suppress thermo-oxidative chain scission during hot-melt processing. Coating lines with narrow slot die gaps of 0.2–0.4 mm require filtration through 100–200 mesh screen packs to remove char particles and undispersed polymer fragments. Adhesion to low-density polyethylene is limited because the nonpolar substrate lacks surface energy; corona treatment to 38–40 mN/m is required for acceptable wet-out.
In melt compounding of post-industrial general-purpose polystyrene recyclate, Asaprene T-420P is added at 6–10 wt% to improve impact toughness while retaining stiffness. The blend is processed on a twin-screw extruder at 190–210 °C with a screw speed of 250–350 r/min and a specific energy input of 0.18–0.25 kWh/kg. Premature feeding of the SBS pellets along with polystyrene granules can cause feeding blockage at the hopper because the softer T-420P deforms under the granule bed; separate side feeding after the first kneading block is preferred. At 8 wt% T-420P, notched Izod impact values under ASTM D256 shift from the brittle range near 2.0 kJ/m² toward 5–8 kJ/m², while tensile strength under ASTM D638-14 decreases by 10–20% relative to unmodified polystyrene. The ductile-brittle transition is visible in injection-molded plaques as stress whitening before crack propagation. Melt flow rate under ISO 1133-1:2022 is reduced by 15–30% depending on the original recyclate. Extrudate swell increases with SBS content, and die openings must be reduced by 5–10% to maintain sheet thickness. Die-lip build-up appears when melt temperature exceeds 225 °C or when the blend is held at temperature for more than 12 h, requiring periodic die-face cleaning. The material must be pre-dried at 70 °C for 2 h if the polystyrene recyclate contains more than 0.2 wt% moisture. Light transmission falls below 70% in 2 mm plaques when T-420P loading exceeds 15 wt%, which limits use in transparent packaging. Production-scale experience indicates that adding more than 10 wt% SBS to high-flow PS recyclate causes screw slip and reduced throughput, particularly on single-screw extruders with smooth feed throats.
Stone mastic asphalt binder modification with Asaprene T-420P is conducted at a dosage of 4–6 wt% for dense-graded asphalt and up to 7–10 wt% for high-stress intersections and bus lanes. The bitumen is heated to 180–190 °C in a vertical tank equipped with an agitator and an external high-shear mill. T-420P pellets are introduced through an eductor at a controlled rate so that the rotor-stator mixer does not cavitate. Mixing for 60–90 min at a shear rate above 3000 s⁻¹ is required to reach a stable polymer network; phase separation can be checked by a static storage test at 180 °C for 48 h. The modified binder is evaluated on a dynamic shear rheometer under AASHTO T 315 for complex shear modulus G*/sinδ before aging. For binders targeting a PG 64-22 grade, G*/sinδ at 64 °C should remain above 1.0 kPa for unaged binder. Multiple stress creep recovery measurements under AASHTO T 350 smooth the non-recoverable creep compliance values. Industrial mixers with paddle agitation alone are insufficient to disperse T-420P, leaving rubbery lumps that block spray bars and reduce storage stability. The maximum safe holding temperature is 195 °C; above this temperature, polybutadiene degradation releases volatile compounds and increases binder viscosity. The maximum storage time at 180 °C should not exceed 24 h without circulation. Laboratory trial batches often show an increase in softening point from 48 °C to 62 °C at 5 wt% SBS addition, while penetration at 25 °C under EN 1426 drops from 65 dmm toward 40 dmm. Crews must ensure the blend is pumped through a 200–500 μm mesh filter before charging the paving machine. Published data for Asaprene T-420P in full asphalt plant trials is limited, but the dosage and high-shear dispersion parameters are within the industrial SBS-modified asphalt envelope.
In melt-cast cap liner compounds, Asaprene T-420P is blended with low-density polyethylene at ratios of 20:80 to 40:60 phr to improve low-temperature opening behavior and reduce cracking during induction sealing. The blend is processed on a cast film line at 180–200 °C, with the melt filtered through 100–150 mesh screens. The addition of T-420P lowers the secant modulus under ASTM D882-18 and improves puncture resistance under ASTM D5748-95(2019). At polyethylene-rich ratios above 60 wt%, the SBS phase has limited compatibility, and interfacial delamination appears as micro-fibrils in the cast film. Blending uniformity is improved by feeding T-420P through the side feeder of a twin-screw compounder rather than dry blending with PE granules. The film haze is higher than unmodified PE, so use is restricted to pigmented or opaque closure liners. Moisture on the PE feedstock causes bubble formation in the melt; both components are pre-dried at 60 °C for 2 h when relative humidity exceeds 60%. The melt should not be held above 210 °C for more than 4 h because the SBS polybutadiene midblock undergoes chain scission and reduces puncture resistance. Production-scale die lines are cleaned with purging compounds that do not contain amine-based additives, which can cause premature crosslinking and black specks. Cap liner thickness is typically 250–900 μm, with lower thickness films requiring higher T-420P content to maintain low-temperature crack resistance.
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Styrene-butadiene-styrene block copolymer T-420P is manufactured by Asahi Kasei under the Asaprene™ trade designation. The grade is a linear triblock elastomer with a bound styrene content of 40 wt% and a polybutadiene midblock. The polymer is supplied as solid pellets and is not oil-extended; formulators control hardness and melt viscosity through separate addition of paraffinic or naphthenic process oils rather than through a preloaded oil fraction. Manufacturer-published data from the certificate of analysis indicate a specific gravity of 0.94 when measured according to ISO 1183-1:2019 and a Shore A hardness of 88 after a 15 s dwell under ASTM D2240-15. The product is used in thermoplastic compounding, hot-melt adhesives, asphalt modification, and footwear soling. In elastomeric compounds, T-420P contributes styrenic physical crosslinks that set room-temperature tensile strength and melt processability, while the butadiene midblock supplies flexibility and recovery. The linear architecture differentiates it from radial SBS grades with identical styrene content by shifting melt tension and high-shear viscosity. Because the grade is supplied without process oil, its effective rubber content per unit mass is higher than oil-extended SBS types containing 30–50 phr paraffinic oil. This distinction matters when comparing prices or blending ratios.
The linear SBS triblock morphology generates physically crosslinked polystyrene domains that soften above the styrene glass transition. For T-420P, the melt mass-flow rate is reported as 20 g/10 min under 200 °C and 5.0 kg load per ISO 1133-1:2022. This value places T-420P in a medium-flow region suitable for injection moulding and extrusion; it is lower than high-flow adhesive grades and higher than low-flow asphalt grades designed for high-shear batch dispersion. Tensile strength of compression-moulded slabs is reported at 24.5 MPa with elongation at break of 750% under ASTM D638-14. The 300% tensile modulus is recorded at 2.9 MPa. Specification control should include bound styrene content, melt mass-flow rate, gel content, and diblock content because batch-to-batch drift in diblock level changes tack and compound hardness even when styrene content remains unchanged.
| Property | Typical value | Test method | Conditions |
|---|---|---|---|
| Bound styrene content | 40 wt% | ASTM D5775-95(2019) | — |
| Specific gravity | 0.94 | ISO 1183-1:2019 | 23 °C |
| Melt mass-flow rate | 20 g/10 min | ISO 1133-1:2022 | 200 °C, 5.0 kg |
| Hardness | 88 Shore A | ASTM D2240-15 | 15 s dwell |
| Tensile strength at break | 24.5 MPa | ASTM D638-14 | 23 ± 2 °C, 50 ± 5% RH |
| Elongation at break | 750% | ASTM D638-14 | 23 ± 2 °C, 50 ± 5% RH |
| 300% tensile modulus | 2.9 MPa | ASTM D638-14 | 23 ± 2 °C, 50 ± 5% RH |
During melt processing on production-scale corotating twin-screw extruders with a 40:1 length-to-diameter ratio, barrel temperatures are typically set between 150 °C and 190 °C from feed throat to die. T-420P does not require predrying when kept in sealed containers below 60% relative humidity; exposed granules are dried at 80 °C for 2 h in a desiccant dryer with a dew point below −40 °C. Melt temperature exceeding 200 °C accelerates oxidative degradation of the polybutadiene midblock, producing viscosity rise, gel particles, and loss of elongation. Single-screw extrusion is feasible only with barrier screws and compression ratios between 2.5:1 and 3.5:1; lower compression can cause feed-throat blockage due to pellet slip. Injection moulding uses mould temperatures from 30 °C to 60 °C to control surface finish and minimize flow marks. Moisture content should be maintained below 0.1 wt% to avoid surface splay. Because published data for this specific configuration is limited, the above conditions reflect standard SBS processing practice rather than a grade-specific moulding trial.
T-420P should not be compounded with amine-based antidegradants or excessive zinc stearate above 0.5 phr because amine residues can accelerate oxidative cross-linking in the polybutadiene midblock. Hindered phenolic antioxidants at 0.1–0.3 phr are preferred for long-term heat ageing. The butadiene midblock controls thermal degradation; process temperatures above 200 °C cause gel formation and a measurable loss of elongation at break. Processing under nitrogen blanketing is used when residence time exceeds 5 min at melt temperatures above 180 °C. Toluene, cyclohexane, and methyl ethyl ketone/toluene blends dissolve the polymer; solution viscosity in 25 wt% toluene at 25 °C is used as a molecular-weight control parameter. Users converting from oil-extended SBS grades must note that T-420P contains no pre-added paraffinic oil. Addition of 30–50 phr naphthenic or paraffinic oil is required to reach hardness values below 70 Shore A in soft compounds. The absence of process oil increases storage stability above 40 °C by reducing oil exudation in warehouse storage.
Hot-melt pressure-sensitive adhesive formulations based on T-420P are compounded with C5 or C9 tackifying hydrocarbon resins and paraffinic process oil in a sigma-blade mixer at 160–180 °C. The linear triblock structure produces lower melt viscosity than radial SBS types at equal tackifier loading, permitting slot-die coating at lower pump pressure. Peel adhesion is assessed according to ASTM D3330/D3330M-04 using 180° peel angle and 300 mm/min jaw separation; loop tack is measured per ASTM D6195-03. A tackifier loading of 80–120 phr is common for removable and permanent label systems, but the exact window requires design-of-experiment work because published data for T-420P in this formulation is limited. Migration kinetics of paraffinic oil in the adhesive matrix affect open time and cold flow; the unbounded oil fraction can be monitored by mass loss after 24 h at 70 °C in a forced-air oven. The lack of oil precharge in T-420P gives the formulator control over plasticizer type and prevents the pre-oil-related softening drift sometimes observed in oil-extended SBS stored above 40 °C.
Substitution of an oil-extended SBS with T-420P in asphalt modification changes the effective bitumen-to-polymer ratio because the polymer phase contains no process oil. Polymer-modified asphalt using SBS at 4–6 wt% is typically dispersed with high-shear mixing at 180–190 °C for 45–60 min. The linear architecture of T-420P can generate a stronger low-shear viscosity increase than radial SBS grades, but storage stability is governed by bitumen maltene composition and sulfur-based coupling. Storage stability is evaluated according to EN 13399, and softening point change is tested per ASTM D36/D36M-14. In footwear compounds, T-420P is blended with general-purpose polystyrene at 20–30 phr to raise Shore A hardness by 3–5 points through reinforcement of the styrenic phase. A twin-screw compounding temperature of 190–210 °C is used to disperse the SBS into a continuous polystyrene matrix. Published comparative data for T-420P in this specific footwear blend is limited; the above hardness shift represents general SBS/PS blend behaviour rather than a manufacturer-guaranteed value.
Regulatory positioning for T-420P must be confirmed against regional food-contact and environmental legislation. The monomer composition falls within styrene-butadiene block copolymers described in US FDA 21 CFR §177.1810 for styrene block polymers, but the final article containing T-420P, not the raw granulate, must be tested for end-use compliance. EU REACH registration under EC 1907/2006 and RoHS Directive 2011/65/EU require absence of lead, cadmium, mercury, hexavalent chromium, PBB, and PBDE at threshold limits; no hazardous substances are declared in the raw polymer according to the safety data sheet. Anti-block additives or pellet coatings added after manufacture can influence a compliance audit. Users requiring medical or food-contact certification must request grade-specific documentation from Asahi Kasei because published data for T-420P in those applications is limited.
Blends of T-420P with general-purpose polystyrene and high-impact polystyrene are processed in corotating twin-screw extruders at 190–210 °C with screw speeds of 300–500 rpm to achieve dispersed SBS domain sizes below 5 µm. The resulting blends show notched Izod impact improvements when tested per ASTM D256-10 at 23 °C; the exact improvement depends on matrix melt flow and SBS loading. At SBS loadings above 30 wt%, co-continuous morphology can reduce tensile strength; the practical loading range for impact modification is 10–25 wt%. Unlike maleic anhydride-grafted SEBS, T-420P is not functionalized, so polyamide and polyester matrices require a separate compatibilizer.
On production-scale twin-screw compounding lines with 40:1 L/D ratio and 250–400 rpm screw speed, replacement of a radial SBS with T-420P reduces melt temperature at equal screw speed because linear triblock chains dissipate less viscous heat in high-shear mixing zones. The lower melt tension relative to radial SBS of similar styrene content may require adjustments in strand pelletizing: a die hole diameter of 3.0 mm and water-bath temperature of 20–30 °C are commonly used to prevent strand sag. In compounds where random styrene-butadiene rubber is replaced, T-420P introduces physical crosslinks that produce room-temperature tensile strength and hot-melt viscosity; however, compression set at 70 °C under ASTM D395-18 is higher than that of vulcanized SBR, reflecting a thermoplastic rather than covalent network structure. Differences in molecular weight distribution and diblock content among SBS grades can shift the processing window by ±5 °C; processors should verify melt flow and gel content before converting from another SBS grade. Capillary rheometry at 180 °C and apparent shear rates from 100 s⁻¹ to 1000 s⁻¹ can be used to quantify the viscosity difference between T-420P and radial grades.