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LCY Chemical Taiwan Globalprene® SBS 1485

    • Product Name: LCY Chemical Taiwan Globalprene® SBS 1485
    • 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 915222
    Product LCY Chemical Taiwan Globalprene® SBS 1485
    Polymer Type Styrene-butadiene-styrene block copolymer (SBS)
    Structure Linear
    Bound Styrene Content 30%
    Oil Content 50 phr
    Density 0.94 g/cm³
    Appearance White to light-yellow pellets
    Volatile Matter ≤0.70%
    Ash Content ≤0.20%
    Tensile Strength ≥15 MPa
    Elongation At Break ≥700%
    300 Modulus ≥2.0 MPa
    Shore A Hardness ≥60
    Permanent Set ≤30%

    As an accredited LCY Chemical Taiwan Globalprene® SBS 1485 factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing LCY Chemical Taiwan Globalprene® SBS 1485 is packaged in 25 kg multiwall paper bags, palletized for industrial handling and shipment.
    Container Loading (20′ FCL) 20′ FCL container loaded with LCY Chemical Taiwan Globalprene® SBS 1485 in 25 kg bags, palletized and secured for ocean shipment.
    Shipping LCY Chemical Taiwan Globalprene® SBS 1485 is shipped as non-hazardous thermoplastic elastomer pellets, typically in 25 kg moisture-barrier bags or 500–1,000 kg jumbo bags on pallets. Store and transport dry, away from heat and direct sunlight; handle as general cargo.
    Storage Store LCY Chemical Taiwan Globalprene® SBS 1485 in a cool, dry, well-ventilated area away from direct sunlight, heat, sparks, flames, and oxidizing materials. Keep containers closed and protect contents from moisture, dust, and contamination. Avoid prolonged high-temperature exposure. Store only in original or compatible containers. Prevent physical damage. Follow first-in, first-out stock rotation and good housekeeping. Ensure adequate ventilation and spill containment.
    Shelf Life Shelf life is 24 months from production date when stored unopened in a dry, cool place, away from sunlight.
    Application of LCY Chemical Taiwan Globalprene® SBS 1485

    What Binder Storage Stability Data Indicate When Polymer-Modified Bitumen Is Produced with SBS 1485

    In polymer-modified bitumen terminal operations, Globalprene® SBS 1485 is metered into penetration-grade road bitumen at 3.0–6.5 wt% based on total binder mass, with high-temperature pavement and bridge-deck formulations commonly held at 4.5–5.5 wt% to meet EN 14023:2010 polymer-modified bitumen specifications. The base bitumen is preheated to 175–190°C in a jacketed vertical tank equipped with low-speed anchor agitation before transfer to a high-shear rotor-stator mill operating at tip speeds above 12 m/s. Dispersing the linear SBS 1485 phase into the maltene continuum under these conditions drives phase inversion, with ASTM D5/D5M penetration values typically reduced by 15–25 dmm and ASTM D36/D36M ring-and-ball softening point increased from 47–49°C to 75–85°C depending on the exact 1485 loading and bitumen source. Elastic recovery under ASTM D6084 at 25°C is used as a release criterion, with values above 75% indicating sufficient polymer network formation. Following high-shear blending, the concentrate is diluted with additional base bitumen or flux oil and maintained at 165–175°C under low-shear circulation; prolonged storage below 165°C in poorly agitated tanks can produce density-driven stratification, with polymer-lean upper layers and polymer-rich lower layers that no longer pass the EN 14023 softening-point difference limit of ≤5°C between top and bottom samples. Terminal operators therefore avoid overhead centrifugal pumps with excessive suction shear and specify heated gear pumps with clearances above 500 µm to limit molecular weight degradation. High-temperature performance grading is checked with AASHTO T315 dynamic shear rheometer at 64°C or 70°C, while low-temperature binder behavior is assessed by AASHTO T313 bending beam rheometer at -12°C to -18°C depending on climate. Published data for grade-specific binder response across all base bitumen sources remains limited, so pilot blending is required before terminal-scale production. The finished polymer-modified binder is loaded into insulated tank trucks with external hot-oil heating and delivered to drum-mix or batch asphalt plants for stone-mastic asphalt, gap-graded dense wearing courses, airport runway overlays, bridge-deck waterproofing membranes, and spray-applied road preservation systems.

    When Footwear Sole Compounds Exceed 45 phr SBS 1485 and the Mold Shrinkage Window Narrows

    In footwear compound production, SBS 1485 is mixed into styrenic thermoplastic elastomer formulations at 20–45 phr alongside crystal polystyrene, naphthenic or paraffinic oil, precipitated calcium carbonate, and 0.1–0.3 phr phenolic antioxidant, with translucent or white unit-sole recipes placing the SBS 1485 content at 30–40 phr. Mixing is carried out in an intermeshing internal mixer at 135–155°C, with a drop temperature not exceeding 160°C to preserve the styrene end-block phase; after fluxing, the batch is sheeted through a two-roll mill at 115–135°C and granulated. Injection molding of sole blanks uses barrel zones of 150/165/170/175°C, a nozzle temperature of 175–180°C, a mold temperature of 25–45°C, and hydraulic injection pressure of 60–90 MPa. When the SBS 1485 loading is raised above 45 phr, the melt exhibits increased shear heating through the check-ring and gate, causing measured melt temperature excursions of 8–12°C above the barrel set point and producing anisotropic shrinkage in the demolded part; holding pressure must then be extended to 8–12 s and mold temperature raised to 40–50°C to maintain dimensional tolerance. Compliance for footwear compounds sold into the European Union is assessed under REACH 1907/2006 Annex XVII restrictions for polycyclic aromatic hydrocarbons in articles, with mechanical testing against ASTM D412-16 tensile strength and elongation, ASTM D624-00 trouser tear, DIN 53516 abrasion loss, and ISO 20871:2018 flexural fatigue. Pre-drying at 70°C for 2 h is required when granulate moisture exceeds 0.1% to avoid surface splay at the gate. Terminal products manufactured from SBS 1485-containing compounds include injection-molded unit soles, foxing strips, wedge soles, direct-injected safety shoe outsoles, molded heel counters, and sole sheets with hardness between 60–85 Shore A.

    Hot-Melt Pressure-Sensitive Adhesive Dispersion and Tackifier Compatibility Limits

    Hot-melt pressure-sensitive adhesive formulations use SBS 1485 at 15–30 wt% with C5 aliphatic or C9 aromatic hydrogenated tackifier resins at 35–55 wt%, plasticizer oil at 10–25 wt%, and hindered phenolic antioxidant at 0.5–1.0 wt%; production is performed in a jacketed sigma-blade or horizontal Z-blade mixer at 155–180°C under a nitrogen blanket to limit oxidative chain scission of the polybutadiene midblock. Brookfield Thermosel viscosity at 160°C is monitored according to ASTM D3236 and is typically held between 2,000 mPa·s and 15,000 mPa·s depending on resin softening point and oil aromaticity; when viscosity exceeds 15,000 mPa·s, slot-die coating onto release liner at 12–25 m/min becomes unstable and edge chatter is observed. Adhesive performance is tested by ASTM D3654 loop tack on stainless steel, ASTM D1876 T-peel at 23±2°C, and ASTM D4498 shear adhesion failure temperature. For adhesive applications intended for incidental food contact, the formulated article is evaluated under FDA 21 CFR 175.105 and EU 10/2011 as applicable, while the polymer itself is supplied under the registrant’s REACH obligation. Operational boundaries include avoiding mixer temperatures above 190°C for more than 60 min and avoiding amine-based stabilizers because they can accelerate oxidative discoloration. End products include paper label stocks, carton sealing tapes, disposable hygiene construction adhesives, mounting tapes, and laminating adhesives where the final adhesive layer is applied at 20–45 g/m² coating weight.

    Thermoplastic olefin and styrenic compound modification with Globalprene® SBS 1485 at 5–15 wt% is performed on 40:1 L/D co-rotating twin-screw extruders with barrel profiles from 160°C at the feed throat to 190–200°C at the die, screw speeds of 250–350 rpm, and gravimetric feeding to maintain pellet-to-pellet consistency. The SBS 1485 pellets are preblended with polypropylene homopolymer or block copolymer, high-crystallinity polyethylene, or high-impact polystyrene, and the polymer melt is passed through a screen changer with 80–120 mesh packs before strand pelletizing. Production-scale compounding on 75 mm twin-screw extruders has shown that melt temperature rises 10–15°C above the set point at screw speeds above 350 rpm due to viscous dissipation, causing edge tearing in the strand and strand pelletizer downtime; barrel zones near the vacuum vent are therefore set 5–10°C lower to reduce foaming. The relevant melt flow rate is measured by ISO 1133-1:2022 at 230°C/2.16 kg or ASTM D1238, tensile properties by ASTM D638-14, notched impact by ASTM D256, and flame classification by UL 94 HB for appliance housings. RoHS compliance is evaluated under EU 2011/65/EU; no halogenated flame retardants are incorporated in standard SBS 1485 compounds. The material is not suitable for continuous load-bearing service above 70°C because the styrene domains soften progressively, and compounds containing migratory external lubricants should be validated for paint adhesion. Terminal articles include injection-molded automotive interior scuff plates, appliance gaskets, toy wheels, extruded weatherseal profiles, and technical profiles requiring low-temperature flexibility.

    In bituminous waterproofing membrane production, SBS 1485 is dispersed into oxidized or modified bitumen at 8–16 wt% of the binder phase, with the balance including 25–35 wt% limestone or talc filler and 0.2–0.5 wt% processing stabilizer; mixing occurs in a horizontal ploughshare or kneader at 170–190°C for 45–75 min until a uniform binder coat is formed. The filled compound is then fed through a calender or extrusion slot die onto a nonwoven polyester or glass-fiber mat at 130–150°C, with sand, slate granules, or PE film applied in-line before cooling drums reduce the sheet temperature to below 35°C for roll winding. Membrane processors report that insufficient mixing time below 45 min leaves undispersed SBS particles that appear as raised gel-like spots on the finished surface and reduce low-temperature flexibility. Compliance and product testing are aligned to EN 13707:2004+A2:2009 for flexible sheets for waterproofing, ASTM D6164 for polymer-modified bituminous sheet materials in roofing, and ASTM D5147 for sampling and testing modified bituminous sheet material; tensile testing uses ASTM D638 or EN 12311-1, with cold bend evaluated according to EN 1109 at temperatures below -15°C depending on the formulation. Storage and transport rolls must be kept upright below 40°C and protected from direct sunlight to prevent blocking. End products include torch-applied roofing membranes, self-adhered underlayments, bridge-deck waterproofing sheets, plaza deck systems, and foundation damp-proofing membranes.

    Solvent-borne construction sealants formulated with SBS 1485 at 10–25 wt% solids are manufactured in high-shear dissolvers by first dissolving the polymer in a mixed aromatic/aliphatic solvent system such as toluene, xylene, or dearomatized white spirit at 20–40% total solids, then adding 20–35 wt% ground calcium carbonate or fumed silica and 0.5–1.0 wt% ultra-violet stabilizer under vacuum to remove entrapped air. The sealant is filled into aluminum or HDPE cartridges through 200–300 µm filters, with final paste viscosity controlled to 80,000–300,000 mPa·s at 25°C by cone-and-plate viscometry. Compliance for construction joint sealants is assessed under ISO 11600:2002 for sealant classification and movement capability, while facade sealants may be evaluated under ETAG 002 or ASTM C920 for joint movement. Mechanical properties are tested according to ASTM D412 for tensile elasticity and ASTM D624 for tear resistance, with accelerated weathering under ISO 4892-2 for xenon-arc exposure. A processing limitation appears when solvent evaporation is too rapid during cartridge application; high aromatic solvent content above 25% of the solvent phase can cause bubble entrapment and poor tooling, while solids below 15% reduce slump resistance below the ISO 11600 class 12.5 movement requirement. Terminal product types include facade movement joints, concrete floor control joints, roof flashing sealants, interior crack sealants, and automotive seam sealants applied by cartridge or bulk pumping systems.

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    Certification & Compliance
    More Introduction

    LCY Chemical Taiwan Globalprene® SBS 1485 is a linear styrene-butadiene-styrene block copolymer supplied for thermoplastic elastomer compounding, bituminous waterproofing modification, hot-melt adhesive formulation, and polymer modification. The product is synthesized by anionic solution polymerization, producing a two-phase morphology in which polystyrene end-blocks form physical crosslinks dispersed in a continuous unsaturated polybutadiene mid-block matrix. Manufacturer-published typical data list bound styrene content at 32.5 wt%, specific gravity at 0.94, and melt flow rate at 8.0 g/10 min under 190 °C/5 kg when measured by ISO 1133-1:2022. These characteristics support both high-shear bitumen blending and conventional thermoplastic processing, provided that the thermal and oxidative limits of the unsaturated mid-block are respected.

    What Thermal Processing Limits Govern Melt Stability in SBS 1485?

    Globalprene® SBS 1485 exhibits a processing window in which melt temperature should not exceed 230 °C for residence times greater than 90 s; above this threshold, the unsaturated polybutadiene mid-block undergoes chain scission and crosslinking, leading to viscosity drift and gel formation. In production-scale compounding on a 40:1 L/D co-rotating twin-screw extruder, barrel zones are typically set between 160 °C and 200 °C, with die temperature maintained at 180–210 °C. Predrying at 80 °C for 2 h is required when ambient relative humidity exceeds 60 % to prevent surface voids from introduced moisture, although the polymer is not highly hygroscopic. The phenolic antioxidant and phosphite costabilizer package in the commercial grade suppresses melt degradation at screw speeds up to 300 rpm, but prolonged hold times above 220 °C can exceed the stabilizer capacity and increase yellowness index beyond 8 on ASTM E313-20.

    For bitumen modification, Globalprene® SBS 1485 is introduced into a high-shear mill at a dosage of 3–6 wt% based on bitumen. The mixer is typically a rotor-stator unit operating at 180–190 °C, with shear rates sufficient to disperse the polymer phase below 10 µm. The resulting polymer-modified bitumen shows an increase in ring-and-ball softening point of 15–30 °C relative to the base bitumen, measured by ASTM D36/D36M-14, and elastic recovery values of 70–85 % when tested by ASTM D6084-13. Dynamic shear rheometer data at 60 °C and 1.6 Hz indicate complex modulus values above 10 kPa and phase angles below 70° for typical polymer-modified bitumen, but published data for this specific configuration is limited because base binder source and modification intensity dominate the rheological response. Storage stability at 163 °C for 48 h is improved by selecting a compatible aromatic process oil; higher paraffinic oil content may promote phase separation and reduce low-temperature ductility.

    Mechanical Property Boundaries in Injection-Molded Test Plaques

    Practitioners evaluating Globalprene® SBS 1485 for injection-molded grips, seals, or overmolded surfaces should establish lot-specific mechanical data using ISO 37:2017 or ASTM D638-14 Type I specimens. The following representative values are extracted from manufacturer technical literature and are not intended as specification limits.

    PropertyTypical valueTest method
    Bound styrene content32.5 wt%ISO 2453:2020
    Specific gravity0.94ISO 2781:2018
    Melt flow rate, 190 °C/5 kg8.0 g/10 minISO 1133-1:2022
    Hardness82 Shore AISO 868:2003
    Tensile strength at break25.0 MPaISO 37:2017
    Elongation at break750 %ISO 37:2017
    300 % modulus3.5 MPaISO 37:2017
    Tear strength45 kN/mISO 34-1:2022

    Dynamic mechanical analysis of SBS 1485 after melt compounding shows a polybutadiene glass transition at −85 °C to −80 °C and a polystyrene glass transition at 95–100 °C; the plateau modulus between these transitions determines elastic recovery. Tan delta peak broadening above 0.3 suggests poor phase separation caused by excessive shear or oil incompatibility. These measurements, obtained by ISO 6721-6:2019 torsional DMA, are used to qualify batch-to-batch variability.

    Compounding with crystal polystyrene at 20 phr raises tensile strength to 28–32 MPa and hardness to 88–92 Shore A, while lowering elongation to 350–450 %. Replacement of 20 phr of polymer with naphthenic oil reduces hardness by 5–8 Shore A and increases melt flow rate by 25–40 %. In a 40:1 L/D twin-screw extruder, the oil is injected downstream after the melting zone to preserve shear intensity for polystyrene end-block dispersion. Process conflicts arise when oil addition exceeds 30 phr: phase inversion may occur, the continuous styrenic network collapses, and tensile values fall below 15 MPa. Such formulations require higher polystyrene loadings to restore physical crosslink density.

    When Unsaturated Mid-Block Chemistry Requires Co-Stabilizer Selection

    Because the polybutadiene mid-block retains unsaturation, the stabilizer system must address both melt-processing consumption and long-term surface degradation in service. A hindered phenolic antioxidant at 0.1–0.5 phr and a phosphite costabilizer at 0.05–0.2 phr are typical in melt-compounded formulations. For outdoor service, carbon black at 2–3 phr or ultraviolet stabilizers such as hindered amine light stabilizers are required; without these additives, exposed injection-molded surfaces can develop microcracks within 500–1000 h of accelerated weathering under ASTM G154-16 cycles. Sulfur-vulcanizing systems may be used when the compound is intended for dynamic rubber-like applications, but amine-based additives should be avoided because they can interfere with phenolic antioxidant activity and promote premature oxidative attack at temperatures above 180 °C.

    In hot-melt adhesive compounding, Globalprene® SBS 1485 is compounded with tackifying resins having softening points of 85–110 °C and with paraffinic or naphthenic process oils. Typical adhesive formulations contain 25–35 wt% SBS 1485, 40–55 wt% tackifier, and 15–25 wt% oil. Viscosity at 180 °C for a 30 wt% polymer formulation is generally 10–30 Pa·s; application by slot-die or roll coater requires viscosities 5–20 Pa·s to avoid ribbing defects. For pressure-sensitive adhesive films, 180° peel adhesion to stainless steel is typically 8–15 N/25 mm after 24 h dwell, measured by ASTM D3330/D3330M-04, and static shear holding power at 1 kg load exceeds 24 h at room temperature. The unsaturated mid-block provides pressure-sensitive tack after compounding but requires storage under a nitrogen blanket to prevent oxidative gelation during prolonged heating above 150 °C.

    Compared to an oil-extended SBS grade containing 30–50 phr extender oil, Globalprene® SBS 1485 is supplied as an unextended polymer, permitting independent selection of aromatic, naphthenic, or paraffinic process oils and avoiding unpredictable migration kinetics from extender oil into adjacent polyolefin substrates. Morphological evaluation by transmission electron microscopy shows polystyrene domain sizes in the 10–30 nm range after melt processing, which strongly influences tensile and elastic recovery performance. In comparison with hydrogenated SEBS grades, SBS 1485 offers lower melt viscosity and higher adhesion to styrenic and bituminous surfaces, but requires antioxidant and ultraviolet stabilization for elevated-temperature or outdoor service because the mid-block is not saturated.

    Selection between Globalprene® SBS 1485 and lower-styrene Globalprene grades depends on the required balance of tensile and low-temperature properties. The higher bound styrene content of 1485 increases the polystyrene physical crosslink density, which elevates modulus, hardness, and tear strength while reducing low-temperature flexibility and elongation. Lower-styrene grades in the same product family exhibit glass transition broadening at lower temperatures and may be preferred for asphalt pavements in cold climates where low-temperature cracking is the dominant failure mode.

    Regulatory documentation for Globalprene® SBS 1485 should be verified with LCY Chemical for the intended application. Under REACH Regulation (EC) No 1907/2006, the polymer is exempt from registration as a substance, but the constituent monomers must be registered by the manufacturer or importer. RoHS compliance is generally declared under Directive 2011/65/EU for the four heavy metals and two brominated flame retardant classes, based on supplier analytical data; the product is not formulated with flame retardants. For adhesive applications regulated under FDA 21 CFR 175.105, compliance must be confirmed for the specific formulation because migrated residual styrene and oligomers are formulation-dependent.

    Regulatory instrumentRelevant scopeVerification basis
    REACH Regulation (EC) No 1907/2006Polymer exemption; monomer registrationSupplier SDS and registration dossier
    RoHS Directive 2011/65/EURestricted heavy metals and brominated flame retardantsSupplier declaration; IEC 62321-5:2013
    FDA 21 CFR 175.105Adhesives in food contactFormulation-specific compliance statement
    ASTM D6084-13Elastic recovery of polymer-modified bitumenLaboratory tensile recovery

    For injection molding, barrel temperatures are set between 170 °C and 200 °C, and injection pressure is typically 70–100 MPa for thin-wall sections. Mould temperature affects surface gloss and weld-line strength; maintaining mould temperatures of 30–50 °C reduces visible flow marks, whereas higher mould temperatures can extend cycle time without improving mechanical integrity. Insufficient venting or excessive screw backpressure above 10 bar may generate melt temperature overshoot and accelerate gel formation. Production-scale observations on toggle-clamp injection machines with clamping force above 800 kN indicate that gate size should be at least 40 % of part wall thickness to prevent jetting and delamination at weld lines.

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