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TSRC Taipol® SBS 4402

    • Product Name: TSRC Taipol® SBS 4402
    • Factroy Site: Yudu County, Ganzhou, Jiangxi, China
    • Price Inquiry: sales8@ascent-chem.com
    • Manufacturer: Ascent Petrochem Holdings Co., Limited
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    Specifications
    HS Code 227729
    Product Name TSRC Taipol® SBS 4402
    Polymer Type Styrene-butadiene-styrene block copolymer (SBS)
    Molecular Structure Radial branched
    Styrene Content 40%
    Butadiene Content 60%
    Density 0.94 g/cm³
    Melt Flow Rate 1.0 g/10 min (200 °C/5 kg)
    Shore A Hardness 92
    Tensile Strength 25 MPa
    Elongation At Break 600%
    300 Percent Modulus 5.0 MPa
    Tear Strength 40 kN/m
    Volatile Matter ≤0.5%
    Ash Content ≤0.2%
    Appearance White powder or crumb

    As an accredited TSRC Taipol® SBS 4402 factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing TSRC Taipol® SBS 4402 is supplied in 25 kg moisture-resistant paper sacks, palletized for industrial handling and storage.
    Container Loading (20′ FCL) TSRC Taipol® SBS 4402 is loaded in a 20′ FCL container as palletized 25 kg bags, shrink-wrapped and strapped for secure transport.
    Shipping TSRC Taipol® SBS 4402 is shipped as a non-hazardous thermoplastic elastomer, typically in 25 kg PE-lined paper bags or big bags on pallets. Keep packaging dry, ventilated, and away from direct sunlight, heat, and moisture. Standard freight applies; no special dangerous-goods classification is normally required.
    Storage Store TSRC Taipol® SBS 4402 in a cool, dry, well-ventilated warehouse, away from direct sunlight, heat, flames, and strong oxidizers. Keep containers tightly closed and pallets off the floor to prevent moisture uptake. Avoid prolonged high temperatures and static buildup; use proper grounding. Store in original packaging, segregate from incompatible materials, and follow local regulations and SDS recommendations.
    Shelf Life TSRC Taipol® SBS 4402 has a shelf life of 24 months when stored in original packaging, cool, dry, and protected from sunlight.
    Application of TSRC Taipol® SBS 4402

    TSRC Taipol® SBS 4402 is a linear styrene-butadiene-styrene block copolymer with a nominal bound styrene content of 40 wt% and a non-staining antioxidant package. In polymer-modified bitumen for heavy-duty road paving, the copolymer is pre-blended with penetration-grade bitumen at 3 wt% to 7 wt%, depending on traffic class and climate zone. The mixing sequence is a two-stage operation. The base bitumen is charged to a jacketed vessel and heated to 175 °C–185 °C. SBS 4402 pellets are added under low-shear propeller agitation to wet out the pellet surfaces. The blend is then passed through a rotor-stator high-shear mill operating at a tip speed of 15 m/s to 25 m/s for 30 min to 60 min. Dispersion is completed in a low-shear paddle mixer held at 170 °C–180 °C for 2 h to 4 h. The terminal binder is sampled for softening point, penetration, elastic recovery, and storage stability. A production failure mode is the formation of gel specks when the high-shear mill temperature exceeds 195 °C or when the finished binder is held above 190 °C for more than 6 h, because the polybutadiene midblock undergoes thermal-oxidative chain scission and coupling. Elemental sulfur may be metered at 0.05 wt% to 0.15 wt% relative to bitumen to stabilize the polymer network and reduce phase separation, but the dosing tolerance is tight at ±0.02 wt%. Sulfur loads above 0.20 wt% produce irreversible gelation and viscosity climb in horizontal storage tanks, and the batch must be downgraded or scrapped. Brookfield rotational viscosity of the modified binder is measured at 135 °C under ASTM D4402. The modified binder is used in dense-graded asphalt concrete for highway overlays, bus lanes, intersection approaches, and airport taxiways where rutting resistance is specified under EN 14023 or ASTM D5976.

    PropertyTest methodCommon specification boundary
    Softening pointASTM D3660 °C–85 °C
    Penetration at 25 °CASTM D540 dmm–70 dmm
    Elastic recovery at 25 °CASTM D6084≥ 75 %
    Storage stability, softening point differenceEN 13399≤ 5 °C

    What Limits Hot-Melt Open Time When SBS 4402 Is Compounded with C5 Resins?

    In pressure-sensitive hot-melt adhesives, SBS 4402 contributes the cohesive elastomer network while C5 aliphatic resins lower plateau modulus and improve room-temperature tack. A reference formulation begins with 100 phr SBS 4402, 80 phr to 150 phr C5 tackifying resin, 0 phr to 50 phr naphthenic or paraffinic process oil, and 1 phr to 2 phr hindered phenolic antioxidant. Compounding is performed in a sigma-blade or z-blade mixer at 160 °C to 175 °C under a nitrogen blanket to limit midblock oxidation. Mixing proceeds for 45 min to 90 min after resin addition until a clear melt is obtained. Melt viscosity is measured at 175 °C with a Brookfield Thermosel under ASTM D3236. The adhesive is coated onto primed polyester or biaxially oriented polypropylene film at 25 g/m² to 50 g/m² using a slot-die hot-melt coater at 160 °C to 180 °C. Open time and loop tack are strongly dependent on oil loading and styrene domain morphology. When oil loading exceeds 50 phr, the melt viscosity falls below 5 000 mPa·s at 175 °C and cohesive strength under shear deteriorates. A formulation limit is observed with high-styrene SBS 4402: at resin loadings above 150 phr, the adhesive loses shear adhesion failure temperature and may show fiber-tear loss on corrugated board below -5 °C. Compliance for food-packaging tapes is evaluated under FDA 21 CFR 175.105 for indirect food contact and REACH Annex XVII for PAH and phthalate restrictions. The terminal products include carton-sealing tapes, label stocks, and diaper assembly adhesives where room-temperature loop tack and die-cut stability are required.

    Bituminous waterproofing membrane production uses a different thermal history from road-bitumen modification. SBS 4402 is pre-compounded into oxidized bitumen at 10 wt% to 15 wt% together with limestone filler at 25 wt% to 35 wt% and a paraffinic process oil at 5 wt% to 10 wt%. The compound is mixed in a vertical high-shear mixer at 180 °C to 190 °C until a homogeneous dispersion is obtained. The molten compound is then fed to a calender or slot-die impregnation line where a polyester nonwoven or spunbond carrier is saturated and double-coated to a finished thickness of 3 mm to 5 mm. The membrane is cooled on a chilled stainless-steel drum and wound with a polyethylene release liner or sanded surface. Production bottlenecks include polymer agglomerates forming on the calender rolls when the compound viscosity is below 1 500 mPa·s at processing temperature. Torch-on membrane performance is verified by EN 13707 for flexible sheets for roof waterproofing, EN 1109 for cold flexibility, and ASTM D5147 for sampling and testing of modified bituminous sheet material. For self-adhesive variants, the cold-flow resistance at 70 °C is assessed under EN 12039. Published tear-strength data for SBS 4402 in polyester-reinforced membrane at sub-zero service temperatures is limited; site qualification is therefore conducted on the finished roll using EN 12310-1 tear propagation and EN 1107-1 dimensional stability. The terminal products are torch-applied roof membranes, self-adhesive underlayments, and below-grade tanking membranes.

    Footwear Sole Compounds and Abrasion Compliance Under ISO 20871

    For injection-moulded footwear sole compounds, the 40 wt% styrene content of SBS 4402 raises hardness and dimensional stability at the expense of low-temperature flex fatigue. A starting formulation combines 100 phr SBS 4402, 25 phr to 45 phr general-purpose polystyrene, 10 phr to 30 phr naphthenic oil, 10 phr to 20 phr calcium carbonate, and 0.5 phr to 1 phr antioxidant. Mixing is carried out in an internal mixer with a fill factor of 0.75 to 0.80 and a drop temperature of 140 °C to 150 °C. The batch is discharged to a two-roll mill at 80 °C to 90 °C for sheeting and pelletizing. Injection moulding uses barrel zones from 150 °C to 190 °C, a mould temperature of 30 °C to 50 °C, and an injection pressure of 60 MPa to 90 MPa. Production failure modes include sink marks when the melt is overdosed with polystyrene above 45 phr, and knit lines when the mould temperature drops below 30 °C. Abrasion resistance is measured under ISO 20871 with a 20 N vertical load using a standard rubber abrasive wheel. Hardness is determined under ASTM D2240, tensile strength and elongation under ISO 37, and trouser tear under ISO 34-1. In European footwear markets, finished soles must be checked against REACH Annex XVII Entry 50 for polycyclic aromatic hydrocarbon limits in rubber articles. The terminal products are direct-injected unit soles, cup-sole bases, and midsoles for casual and sports-style footwear where high hardness and moderate slip resistance are required.

    When SBS 4402 is dry-blended with general-purpose polystyrene for injection-moulded rigid goods, the block copolymer functions as an impact modifier at loadings from 10 wt% to 25 wt%. The blend is processed through a co-rotating twin-screw extruder with an L/D ratio of 40:1 and a screw speed of 300 min⁻¹ to 500 min⁻¹. Barrel temperatures are profiled from 180 °C to 210 °C, and the strand pelletizing die is held at 200 °C. Residence time below 120 s is required to prevent thermal degradation of the polybutadiene soft block. The extrudate is cooled in a water bath at 30 °C to 40 °C and pelletized to 3 mm to 4 mm cylindrical granules. Notched Izod impact strength is tested under ASTM D256 at 23 °C and -20 °C, tensile modulus under ASTM D638, and melt mass-flow rate under ISO 1133-1:2022. A processing incompatibility is observed when the compound is purged with rigid PVC containing organotin stabilizers; mixed regrind streams can generate hydrogen chloride and degrade the SBS midblock. The use of regrind is therefore limited to 20 wt% in thin-wall parts. The end products include appliance housings, office-machine covers, and toys that require compliance with EN 71-3 migration limits and REACH Annex XVII plasticizer restrictions.

    When SBS 4402 Replaces Methylene Chloride-Soluble Binders in Solvent Contact Adhesives

    A solvent-borne SBS 4402 contact adhesive is compounded at 18 wt% to 25 wt% solids in a blend of toluene, acetone, and n-hexane. The polymer is first swollen in the solvent mixture under low-speed agitation for 4 h to 6 h in an explosion-proof disperser. A tackifying resin, typically a C5 hydrocarbon resin or glycerol ester of rosin, is added at 40 phr to 80 phr on polymer solids. The adhesive is applied by brush or spray to both substrates and dried for 15 min to 30 min at 23 °C and 50 % relative humidity. Open assembly time is controlled by solvent retention and skin formation; a toluene-rich solvent system extends bond time but increases volatile organic compound emissions. The product must be formulated below local VOC emission limits, with installation-level requirements referenced under Directive 1999/13/EC. Peel adhesion on flexible foam and leather is measured under ISO 11339 at a separation speed of 100 mm/min. Heat resistance is assessed by lap shear testing of bonded beechwood specimens under ISO 4587 after 7 d at 23 °C. An incompatibility is noted when ketone solvents exceed 30 wt% of the solvent blend; polar ketones accelerate phase separation and lower final bond strength on styrene-rich substrates. The terminal products are footwear upper bonding adhesives, upholstery contact adhesives, and furniture foam assembly adhesives.

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    Certification & Compliance
    More Introduction

    TSRC Taipol® SBS 4402 is a linear styrene-butadiene-styrene thermoplastic elastomer with a nominal bound styrene content of 40 wt%. The grade is supplied as a non-oil-extended pellet and is classified under CAS 9003-55-8. Its molecular architecture consists of polystyrene end-blocks and a polybutadiene mid-block, yielding a two-phase morphology in which the polystyrene domains act as physical crosslinks below the styrene glass transition temperature. This morphology permits melt reprocessing while retaining elastomeric recovery after solidification. Published manufacturer data place the melt flow rate at 2.0 g/10 min under 190°C/5 kg loading when tested to ASTM D1238. Because the grade is not oil-extended, the compounder retains control over the addition of naphthenic or paraffinic process oils instead of receiving a pre-softened product. The product is used in bituminous binder modification, hot-melt adhesives, footwear compounding, and as a toughening modifier in polymer blends.

    What Are the Standard Specification Parameters Published for Taipol SBS 4402?

    Specification controls for the grade are reported against the following test standards. Values are representative unfilled resin data and not formulation-specific maxima or minima unless stated.

    PropertyTypical valueTest method
    Bound styrene content40 wt%ISO 22768
    Melt flow rate2.0 g/10 minASTM D1238, 190°C/5 kg
    Specific gravity0.94ASTM D792
    Tensile strength18 MPaISO 37
    Elongation at break700%ISO 37
    Hardness85 Shore AISO 868
    300% modulus2.5 MPaISO 37
    Volatile matter< 0.5%ASTM D5668
    Total ash< 0.2%ISO 247

    The 300% modulus value reflects the stiffness contribution of the polystyrene domains after the polybutadiene mid-block is extended. Melt flow rate may also be determined on dried pellets per ISO 1133-1:2022 as an alternative to ASTM D1238. Hardness specimens are compression molded and conditioned for 24 h at 23°C and 50% relative humidity before measurement.

    Because the grade is linear rather than radial, melt elasticity and die swell are lower than those of radial SBS counterparts with similar styrene content. This is relevant in profile extrusion and adhesive coating, where high die swell produces dimensional instability. The linear architecture also narrows the processing window in blown film applications because melt strength decreases more rapidly as temperature exceeds 190°C.

    Commercial compounding of Taipol SBS 4402 is conducted on co-rotating twin-screw extruders with L/D ratios between 40:1 and 52:1. Barrel set points from 150°C to 185°C are maintained, while the feed throat is cooled to 40°C to prevent pellet bridging. At screw speeds above 250 rpm, viscous dissipation can raise melt temperature above 200°C; sustained operation in this regime initiates oxidative chain scission and gel formation. The pellets should be dried at 65°C for 2–4 h when pellet surface moisture exceeds 0.08% or when ambient relative humidity exceeds 60%. On a 75-ton injection molding machine with a 25 mm diameter reciprocating screw, a melt temperature of 175°C and a back pressure of 0.5 MPa are representative starting conditions for tensile test plaques conforming to ISO 37. Post-molding shrinkage of 1.5% to 2.0% is observed in unfilled injection-molded plaques; production shrinkage should be revalidated per ASTM D955. For high-shear dispersion in bitumen or adhesive manufacture, a rotor-stator mixer with a tip speed of 15–25 m/s is preferred over low-speed propellers, which produce insufficient elongational stress to disrupt the elastomer domains. Residence time in the high-shear zone should not exceed 45 min to avoid excessive viscosity reduction from chain scission.

    In hot-melt adhesive formulations, Taipol SBS 4402 is compounded with hydrocarbon tackifiers and paraffinic or naphthenic process oils. The 40 wt% styrene block content provides cohesive strength at 23°C, while the polybutadiene mid-block contributes pressure-sensitive tack after high-shear mixing. Formulation viscosity is governed by the thermoplastic phase: at 160°C, melt viscosity permits application by slot-die or bead dispensers when the compound is formulated to a Brookfield viscosity of 5,000–20,000 mPa·s. Tackifier compatibility is limited to C5/C9 aliphatic-aromatic resins with softening points between 90°C and 110°C; high-polarity rosin esters can phase-separate and produce surface haze. In pressure-sensitive adhesive coatings, the mid-block is selectively crosslinked with diisocyanates to elevate shear holding power. Published data for this specific configuration is limited; screening with a loop-tack or falling-ball tack test is required before production qualification. Thermal stability of the formulated adhesive should be evaluated by holding the molten compound at 175°C for 72 h and measuring color change to ensure no gelation.

    When Taipol SBS 4402 Replaces Lower-Styrene SBS in Bituminous Binder Modification

    Addition of 3–5 wt% Taipol SBS 4402 to a high-shear bitumen mixing vessel at 180°C increases the softening point and elastic recovery of the binder. In comparison with SBS grades having a 30 wt% nominal styrene content, the 40 wt% styrene content of Taipol SBS 4402 produces a denser polystyrene network and a higher softening point, but raises the mixing viscosity and can reduce low-temperature elongation. The higher styrene content also raises the elastic modulus of the bitumen after cooling, which is relevant for rutting resistance under 60°C wheel tracking. Storage stability of polymer-modified bitumen should be evaluated under EN 13399 or ASTM D7175, with phase separation measured after 72 h at 180°C. High-shear dispersion at 3,000–5,000 rpm using a rotor-stator mill is required to break the pellet domains into the bitumen phase; inadequate shear leaves visible gel bodies. In paving operations, compaction temperatures are typically 10–20°C higher than for unmodified binders. The use of a crosslinking agent, such as elemental sulfur at 0.1–0.3 wt% of binder, improves storage stability but shortens workable mix time.

    Thermal Stability Boundaries Under Prolonged Residence

    Thermal stability boundaries are defined by the polybutadiene mid-block, which is susceptible to autoxidation at process temperatures above 190°C. A standard factory antioxidant package is incorporated, but when compounding requires residence times above 4 min, an additional 0.1–0.3 phr of a phenolic antioxidant plus a phosphite co-stabilizer is used. Melt viscosity at 190°C increases irreversibly if the molten material is held under air for more than 20 min, indicating crosslinking. Processing under nitrogen blanketing is recommended for prolonged purges. The material should not be combined with amine-based antioxidants that can deactivate phenolic synergists; this incompatibility can produce surface bloom and raise yellowness index. Differential scanning calorimetry oxidation induction time testing at 180°C under oxygen may be used as an incoming quality check; values below 10 min indicate antioxidant depletion.

    Relative to oil-extended Taipol SBS grades, Taipol SBS 4402 is supplied without extender oil; this removes oil migration during storage but increases the energy required for melt dispersion. In shoe-sole compounds, the grade is blended with general-purpose polystyrene and impact modifiers at 20–40 phr to balance abrasion resistance and flex crack growth. Injection-molded soles show a density of 0.94 g/cm³, which is lower than PVC or vulcanized rubber alternatives. Aliphatic hydrocarbon fluids and strong oxidizers should be avoided because they cause softening or chain scission. In polymer modification, addition of 5–15 wt% of Taipol SBS 4402 to polypropylene or polystyrene shifts the notched Izod impact failure mode from brittle fracture to ductile tearing, but light transmission decreases as the dispersed domain size increases. Outdoor weathering data for this specific application are limited; exposure testing under ASTM G155 is required before specification of a stabilization package. Packaging is typically 25 kg multi-walled bags or 1,000 kg flexible intermediate bulk containers, and the pellets should be stored below 40°C away from ultraviolet light.

    For food-contact and medical packaging applications, unfilled SBS is not intrinsically compliant with FDA 21 CFR 177.1810 or EU Regulation 10/2011; specific migration testing and formulation-specific limitations are required. The grade should not be used in applications involving prolonged contact with strong oxidizing media, aromatic solvents, or chlorinated hydrocarbons because these agents swell the polystyrene domains or degrade the polybutadiene mid-block.

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