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LCY Chemical Huizhou Globalprene® SBS 1475

    • Product Name: LCY Chemical Huizhou Globalprene® SBS 1475
    • Factroy Site: Yudu County, Ganzhou, Jiangxi, China
    • Price Inquiry: sales8@ascent-chem.com
    • Manufacturer: Ascent Petrochem Holdings Co., Limited
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    VTB
    Specifications
    HS Code 480743
    Polymertype Styrene-butadiene-styrene (SBS) block copolymer
    Blockstructure Linear triblock
    Styrenecontent 30%
    Butadienecontent 70%
    Density 0.94 g/cm³
    Meltflowrate 5 g/10 min (200°C/5 kg)
    Hardnessshorea 75
    Tensilestrength 20 MPa
    Elongationatbreak 700%
    300percentmodulus 3 MPa
    Solutionviscosity 1500 mPa·s (25% toluene, 25°C)
    Volatilematter ≤0.5%
    Ashcontent ≤0.2%
    Appearance White to light yellow pellets

    As an accredited LCY Chemical Huizhou Globalprene® SBS 1475 factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing LCY Chemical Huizhou Globalprene® SBS 1475 is packaged in 25 kg net paper bags, palletized for industrial handling.
    Container Loading (20′ FCL) 20′ FCL container loaded with LCY Chemical Huizhou Globalprene® SBS 1475 in securely stacked bags, palletized and sealed for export shipment.
    Shipping LCY Chemical Huizhou Globalprene® SBS 1475 is a non-hazardous, solid thermoplastic elastomer, not regulated for transport under UN, IMDG, or IATA rules. It is typically supplied in moisture-resistant 25 kg bags, palletized, and shipped by standard sea or land freight; keep dry, cool, and away from direct sunlight and ignition sources.
    Storage Store LCY Globalprene® SBS 1475 in a cool, dry, well-ventilated warehouse, away from direct sunlight, heat, sparks, flames, and strong oxidizers. Keep packages tightly closed and elevated off floors to prevent moisture uptake. Avoid prolonged elevated-temperature storage; rotate stock oldest first. Maintain good housekeeping to control dust and prevent slips.
    Shelf Life Shelf life is typically 24 months from production when stored unopened in a cool, dry, ventilated area, away from sunlight and moisture.
    Application of LCY Chemical Huizhou Globalprene® SBS 1475

    During production of polymer-modified bitumen from LCY Chemical Huizhou Globalprene® SBS 1475, penetration-grade binder is preheated in a jacketed vessel equipped with a high-torque anchor agitator and a recirculation loop. SBS 1475 is introduced into the binder vortex at 4.0–6.0 wt% for dense-graded wearing courses; stress-absorbing membrane interlayers and sprayed waterproofing compounds are formulated at 6.5–8.0 wt% polymer content. Because SBS 1475 is a linear styrene-butadiene-styrene triblock, swelling in the maltene fraction proceeds rapidly under shear, but the finished PMB may require sulfur-based stabilisation at 0.05–0.15 wt% to suppress storage separation. Dispersion is completed through a rotor-stator high-shear mill with tip speed between 15 m/s and 25 m/s, held at 175–190 °C for 90–180 min. Temperature above 200 °C accelerates oxidative degradation of the polybutadiene midblock and reduces elastic recovery. Finished binder is graded under EN 14023:2010, with softening point tested to EN 1427:2015, penetration to EN 1426:2015, elastic recovery to EN 13398:2017, and storage stability to EN 13399:2017. The PMB is used in stone mastic asphalt and porous friction courses, where rut resistance and low-temperature cracking resistance are specified within EN 13108-2:2016.

    For milled asphalt overlay work, the same SBS 1475-modified binder is often supplied as a ready-to-use polymer-modified bitumen requiring no additional field blending. Storage tanks on the mixing plant are held at 160–170 °C under slow agitation to prevent local polymer agglomeration near heating coils. Viscosity stabilisation is checked before discharge because SBS-rich PMB can exhibit shear-rate-dependent viscosity; a Brookfield viscosity above 3,000 mPa·s at 135 °C can impair pumping through the bitumen spray bar. The downstream asphalt mix is produced at 160–180 °C aggregate temperature, and compaction is typically completed before the mat cools below 130–135 °C. These process windows are critical because SBS 1475 contributes elasticity only when the polymer phase forms a continuous or co-continuous network; insufficient compaction temperature leaves interconnected voids and lowers indirect tensile strength ratio after moisture conditioning.

    Can a 75-phr SBS 1475 Unit Sole Compound Retain DIN 53516 Abrasion Resistance After High-Shear Kneading?

    Footwear soling compounds are prepared on a two-roll mill or in a Banbury-type internal mixer with a drop thermocouple setpoint of 130–150 °C. A starting-point unit sole formulation uses 75.0 phr SBS 1475, 25.0 phr general-purpose polystyrene, 30.0–40.0 phr naphthenic oil, 5.0–10.0 phr precipitated silica, and 0.3–0.5 phr of a hindered phenolic antioxidant. Mixing sequence is controlled because SBS 1475 fluxing before polystyrene addition prevents phase inversion and lowers peak torque on the mixer gearbox. Oil is injected incrementally only after the SBS/polystyrene melt has formed; early oil addition causes mill roll slippage and poor dispersion. A two-roll mill operating at 40–60 °C front roll and 35–50 °C rear roll is used for slab-off, and the batch is then granulated for injection moulding. Injection moulding uses a reciprocating screw with compression ratio 2.5:1 to 3.5:1, nozzle temperature 170–190 °C, mould temperature 25–40 °C, and holding pressure 40–60 MPa. Tensile properties are measured per ASTM D412-16 using die C, tear strength per ASTM D624-00, and abrasion per DIN 53516. The finished unit soles, midsoles, and foxing components are accepted for high-wear use when abrasion loss is below 250 mm³. At SBS 1475 loadings above 80 phr, die swell and cycle time increase beyond the limits of high-volume multicavity moulds.

    Hot-Melt Pressure-Sensitive Adhesive Viscosity Plateaus and Tackifier Compatibility Limits

    In hot-melt pressure-sensitive adhesive compounding, SBS 1475 is dissolved in a sigma-blade mixer at 160–180 °C under a nitrogen blanket to limit oxidative gelation of the butadiene midblock. Assembly-label adhesives typically contain 22–30 wt% SBS 1475, 35–45 wt% C5 aliphatic tackifier with softening point 90–105 °C, 15–25 wt% naphthenic oil, and 0.5–1.0 wt% antioxidant package. The mixer is operated at 30–60 rpm until the SBS phase is fully solubilised and the Brookfield viscosity at 180 °C falls within 15,000–60,000 mPa·s for slot-die coating. A rise in viscosity after the plateau indicates gel body formation or phase separation; the batch is then rejected for coating line use. Adhesives for food-contact packaging are evaluated under FDA 21 CFR 175.105 and EU 10/2011, where migration of styrene and low-molecular-weight species is controlled. Loop tack is measured with ASTM D6195-22, peel adhesion with ASTM D3330/D3330M-04, and holding power with ASTM D4498-07. Continuous shear performance degrades above 70 °C because the styrene domains soften and creep accelerates. Published data for SBS 1475 in this specific configuration is limited, so end-use qualification at 50 °C and 70 °C is required before specification of coated tape and label stock.

    For post-consumer high-density polyethylene regrind, SBS 1475 is compounded as an impact modifier in a co-rotating twin-screw extruder with 40:1 L/D and segmented shear elements. The compounding ratio is 8–12 wt% SBS 1475 in the regrind; below 8 wt%, low-temperature Izod improvement is insufficient for export crate service, while above 12 wt%, the melt becomes overelastic and causes die swell at the strand face. Barrel temperatures are profiled from 180 °C in the feed zone to 220 °C near the die, and melt temperature above 230 °C is avoided because the polybutadiene segment degrades and volatile butadiene-related species are generated. Screw speed is matched to a specific mechanical energy input of 0.18–0.25 kWh/kg, ensuring dispersion without excessive residence time. The modified regrind is pelletised and injection-moulded into crates, pallet feet, and automotive wheel-arch liners. Flexural modulus is determined by ISO 178:2019, notched Izod impact by ASTM D256-23, and melt mass-flow rate by ISO 1133-1:2022 at 190 °C/2.16 kg. At 12 wt% SBS 1475 loading, tensile modulus decreases by 15–25% relative to the unmodified regrind, so the compound is not used where top-load rigidity is controlled to ASTM D2659-16 for rigid packaging.

    When movement joint sealants require elastic recovery above 80% at −20 °C

    Butyl and polybutene-based construction sealants are compounded with SBS 1475 in a Z-blade mixer under vacuum of −0.08 MPa to −0.09 MPa to remove entrained air and residual moisture. A movement joint formulation uses 10–15 wt% SBS 1475, 35–45 wt% ground calcium carbonate, 20–30 wt% polybutene plasticiser, 3–5 wt% hydrogenated rosin ester, and 0.2–0.5 wt% moisture scavenger. The batch is mixed at 120–140 °C for 45–90 min; SBS 1475 is added after filler wet-out to limit high-torque peaks on the mixer gearbox. The finished sealant is tested for slump under ISO 7390:2003, elastic recovery under ISO 7389:2003, and joint movement performance under ISO 11600:2011 Class F and ASTM C920-18 Type S Grade NS. Tooling time is typically 10–20 min at 23 °C and 50% RH. The material is gunned into façade expansion joints, perimeter window seals, and cold-room panel joints. SBS 1475 is not suitable for acetoxy silicone chemistry or amine-cured polysulfide systems; such combinations cause immediate phase separation and premature hardening.

    Soft-touch TPE-S compounds are formulated with SBS 1475 for overmoulding onto polypropylene substrates; interfacial melt bonding depends on maintaining a co-continuous polypropylene-rich phase at the tool surface. The compound contains 35.0–45.0 wt% SBS 1475, 15.0–20.0 wt% polypropylene homopolymer with melt flow rate 25 g/10 min, 30.0–40.0 wt% paraffinic oil, and 0.3–0.5 wt% antioxidant. Compounding is run on a co-rotating twin-screw extruder with 32:1 to 40:1 L/D, with oil injection after polymer flux at barrel zone 5 of 9. For toys and consumer goods, compliance is documented under EN 71-3:2019+A1:2021 migration limits and REACH SVHC screening. Mechanical properties are checked per ISO 37:2017, hardness per ISO 48-4:2018, and compression set per ISO 815-1:2019. Finished grips are characterised by hardness 55–70 Shore A and melt flow sufficient for two-shot injection; adhesion to polypropylene is influenced by barrel temperature between 190–210 °C and mould temperature 30–50 °C. SBS 1475-based TPE-S is not specified for prolonged contact with mineral oils or aromatic solvents because the butadiene segment swells and hardness decreases significantly.

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    Certification & Compliance
    More Introduction

    LCY Chemical Huizhou supplies Globalprene® SBS 1475 as a linear styrene-butadiene-styrene thermoplastic elastomer in pellet form. The product is classified under CAS 9003-55-8 and is manufactured without extender oil, a deliberate departure from oil-extended SBS grades that carry 33 phr or 50 phr paraffinic or naphthenic oil. The linear molecular architecture comprises polystyrene end-blocks that phase-separate into glassy domains and a polybutadiene midblock that provides elastomeric recovery. Distributor literature assigns the grade a bound styrene content of approximately 40 wt%, placing it between lower-styrene grades optimized for low-temperature flexibility and higher-styrene grades optimized for hardness and tensile strength. This styrene content, together with the absence of extender oil, is the primary variable that controls downstream compound viscosity, filler acceptance, and room-temperature tensile response.

    Does 1475 Require Predrying Before Twin-Screw Compounding?

    Predrying is not mandatory when ambient relative humidity is below 60%. The pellet is porous, so surface moisture uptake in southern China monsoon conditions above 75% RH can generate vent foaming on 65 mm co-rotating twin-screw extruders operating with L/D 44. In those conditions, a hopper-air dryer at 60°C for 2 h reduces surface moisture to below 0.05 wt%. Barrel set points from 150°C at the feed throat to 190°C at the die maintain melt temperature below 210°C. If melt temperature exceeds 215°C, residence time should remain under 2 min because the unsaturated butadiene midblock undergoes oxidative coupling. Degradation is first observed as a rise in die pressure and a shift from water-white to yellow-amber, followed by gel particles in cast film. Melt flow rate per ASTM D1238 at 200°C/5 kg is typically 2 g/10 min; a production QC limit of ±15% drift after 4 h extrusion avoids running degraded regrind. The same thermal boundary applies to injection molding, but screw recovery time in a 120-ton injection molding machine should be watched when back pressure exceeds 10 bar.

    Representative physical properties for the neat polymer are tabulated below. The values are manufacturer-reported typical data from compression-molded specimens and are not specification limits; the certificate of analysis for a specific lot governs incoming QC.

    PropertyTypical valueTest method
    Specific gravity0.94ASTM D792
    Shore A hardness72ASTM D2240
    Tensile strength18 MPaASTM D638
    300% modulus3.0 MPaASTM D638
    Elongation at break750%ASTM D638
    Melt flow rate2 g/10 min at 200°C/5 kgASTM D1238
    Bound styrene40 wt%Fourier-transform infrared, internal method

    These properties are not directly comparable with oil-extended SBS because extender oil reduces hardness and tensile strength by dilution. The 300% modulus value is meaningful only when specimens are conditioned at 23 ± 2°C and 50 ± 5% RH per ISO 291.

    Tensile Properties and the 300% Modulus Boundary

    Tensile data for SBS 1475 are generated on die-cut Type IV specimens per ASTM D638 at 500 mm/min. At approximately 40 wt% bound styrene, the room-temperature stress-strain response shows strain-induced crystallization of the butadiene midblock; this raises tensile strength but increases tensile set relative to lower-styrene SBS grades. The 300% modulus near 3.0 MPa is a useful formulation boundary. Addition of 5–10 phr of a styrenic block resin raises the modulus by approximately 20%, whereas 15 phr of naphthenic oil depresses it below 2.0 MPa and reduces abrasion resistance in unfilled systems. This differs from star-branched SBS grades, which at comparable styrene content often show lower die swell and higher melt strength but lower elongation because of restricted chain relaxation. Compounds requiring tensile strength above 22 MPa should be reformulated with a higher-styrene SBS, or reinforced with precipitated silica above 30 phr, but silica above this loading increases compound viscosity and requires silane coupling treatment for adequate dispersion.

    In footwear outsole compounds, Globalprene® SBS 1475 is typically combined with polystyrene or high-styrene SBS at 10–30 phr and naphthenic oil at 10–25 phr to adjust hardness and mixing torque. A 55 L Banbury mixer or 58 mm intermeshing twin-screw extruder disperses the polymer; ram pressure is raised only after pellets soften to avoid rotor stalling. The addition sequence affects mix time: polymer, polystyrene, and antioxidant are introduced first, followed by oil after fusion. Adding all oil at time zero increases slip and can extend mix time by approximately 30%. Fillers such as calcium carbonate or silica above 20 phr are preferably side-fed because the high low-shear viscosity of the neat block copolymer tends to encapsulate filler aggregates. Molded parts demolded below 40°C exhibit lower surface tack and reduced sticking to aluminum molds. For direct injection onto fabric, substrate preheating to 60–80°C improves bond strength because it minimizes premature quench of the SBS melt at the fabric interface.

    When 1475 Is Used in Hot-Melt Pressure-Sensitive Adhesives

    In hot-melt pressure-sensitive adhesives, 1475 is dissolved in a hydrocarbon or rosin ester tackifier system at 160–180°C in a sigma-blade mixer. The aromatic content and softening point of the tackifier govern the glass transition of the polystyrene end-block domains; with 100–120 phr of a C9/C5 hybrid tackifier, shear adhesion failure temperature generally increases. Because the polymer is unextended, hot-melt viscosity is controlled by the processor rather than residual extender oil. Nitrogen blanketing is recommended above 170°C because the unsaturated butadiene midblock undergoes oxidative chain scission in air, causing viscosity drift. Published data for the diblock content of this specific configuration are limited; formulators should request the lot-specific certificate of analysis if low diblock content is critical for high-temperature cohesive strength. Addition of 15–25 phr liquid polybutene compensates for insufficient loop tack but reduces cohesive strength at 70°C. Tack values are not intrinsic to SBS 1475 because loop tack in SBS adhesives is dominated by tackifier composition and coating weight. For pressure-sensitive adhesive tapes, the formulation is usually coated at 25–75 g/m² dry coating weight; below 25 g/m², adhesion to low-energy surfaces becomes inconsistent.

    Compared with oil-extended SBS grades, 1475 has higher neat Shore A hardness because there is no extender oil to soften the matrix. The processor must add oil explicitly; this is an advantage when tight control of plasticizer level is required but a disadvantage in low-shear mixing because the neat polymer has higher viscosity. The absence of extender oil also removes the problem of oil migration to the surface of stacked molded parts stored above 40°C, a failure mode observed in oil-extended compounds. Compared with higher-styrene SBS grades near 45–50 wt% styrene, 1475 gives lower compound viscosity and better butadiene-phase tack, but approximately 20–30% lower tensile strength in the same unfilled formulation. Compared with lower-styrene grades near 30 wt% styrene, 1475 gives higher hardness and tensile strength but less low-temperature flexibility. Any substitution of 1475 for a radial or star-branched SBS should be verified by measuring die swell and melt strength on the actual extrusion or blow-molding line.

    CharacteristicGlobalprene SBS 1475Oil-extended SBS familyHigher-styrene SBS family
    Extender oilnone33–50 phrnone
    Bound styrene40 wt%30–35 wt%45–50 wt%
    Shore A hardness7245–6080+
    300% modulus3.0 MPa<2.0 MPa>4.0 MPa
    Tensile strength18 MPa8–12 MPa22–30 MPa
    Melt viscositymediumlowhigh
    Primary processing boundarythermal degradation above 215°Coil migration above 40°Chigh torque, higher die pressure

    Bitumen modification with SBS 1475 requires high-shear mixing at 180–190°C for 60–90 min. The polymer absorbs maltene-type fractions and swells; at 4–6 wt% SBS addition to paving-grade bitumen, the softening point typically rises by 20–30°C under ASTM D36. Unlike lower-molecular-weight SBS grades that disperse rapidly but lose elastic recovery during hot storage, 1475 tends to form a continuous polymer-rich network. Phase separation after 48 h at 160°C is observed in base bitumens with high asphaltene content unless 2–5 wt% aromatic oil or a compatibility agent is added. The maltene/asphaltene ratio should remain above 1.5 to maintain storage stability; below this boundary, the same polymer loading that improves rutting resistance can produce unacceptable phase separation. For roofing membranes, 8–10 wt% SBS is used with a stabilizer package to limit thermo-oxidative degradation. In direct comparison with ethylene-vinyl acetate copolymer-modified bitumen, SBS 1475 provides higher elastic recovery at 60°C but requires higher mixing energy and is more sensitive to oxidative degradation if the mixer is not inert-gas blanketed.

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