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LCY Chemical Globalprene® SBS 1484

    • Product Name: LCY Chemical Globalprene® SBS 1484
    • 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 209884
    Polymer Type styrene-butadiene-styrene block copolymer
    Block Structure linear triblock
    Styrene Content 30–32 wt% (typical)
    Butadiene Content 68–70 wt% (typical)
    Density 0.93–0.95 g/cm3
    Melt Flow Rate 5–7 g/10 min (200 °C/5 kg, typical)
    Shore A Hardness 72–78
    Tensile Strength 20–26 MPa
    Elongation At Break 650–750%
    300pct Modulus 2.0–3.0 MPa
    Tear Strength 25–35 kN/m
    Solution Viscosity 1000–1500 mPa·s (25 wt% in toluene, typical)
    Volatile Matter ≤0.5 wt%
    Ash Content ≤0.2 wt%

    As an accredited LCY Chemical Globalprene® SBS 1484 factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Supplied in 25 kg moisture-barrier bags, palletized, with LCY Chemical Globalprene® SBS 1484 markings and batch labels.
    Container Loading (20′ FCL) LCY Chemical Globalprene® SBS 1484 is loaded in 25 kg bags into a 20-foot FCL, palletized and secured for export shipment.
    Shipping LCY Chemical Globalprene® SBS 1484, a non-hazardous SBS block copolymer, is shipped as general cargo in 25 kg bags or jumbo bags. Keep dry and cool in ventilated conditions, protect from moisture, direct sunlight, contamination, and excessive heat, and avoid ignition sources during handling and transport.
    Storage Store in original sealed packaging in a cool, dry, well-ventilated warehouse, away from direct sunlight, heat, flames, and oxidizers. Protect from moisture, contamination, and prolonged UV exposure; keep containers closed. Use first-in, first-out stock rotation, stack pallets securely to prevent deformation, and follow the SDS and local regulations.
    Shelf Life LCY Chemical Globalprene® SBS 1484 typically has a 24-month shelf life when stored cool, dry, and in sealed original packaging.
    Application of LCY Chemical Globalprene® SBS 1484

    In torch-applied SBS-modified bitumen membrane compounding, LCY Chemical Globalprene® SBS 1484 establishes a continuous polymer-rich phase only after the addition ratio crosses approximately 8 wt%; below this loading the compound behaves as a polymer-dispersed bitumen with limited elongation recovery under ASTM D6084-18. The polymer is dispersed into oxidized bitumen preheated to 160–175 °C using a heated rotor-stator mill with a radial gap of 0.4–0.6 mm and a rotor speed of 2,500–3,500 rpm. SBS 1484 crumb is introduced at a controlled rate to avoid wetting failure; dispersed-phase inspection for undispersed gel particles is performed after 30 min and again after 45 min. If the batch temperature exceeds 195 °C for more than 20 min, the butadiene segment undergoes thermo-oxidative chain scission, producing a measurable increase in penetration under ASTM D5-19 and a loss of low-temperature flexibility under EN 1109:2013. On production lines using this rotor-stator configuration, batch-to-batch melt viscosity at 180 °C typically shifts ±10% when the base bitumen source changes from straight-run vacuum distillation to visbroken feedstock.

    Industry compliance for the membrane system is anchored to EN 13707:2013 for reinforced bitumen sheets for roofing and EN 13969:2010 for bridge-deck waterproofing systems; membrane testing is performed under ASTM D5147-18. The compound formulation addition ratio is 8–14 wt% SBS 1484, 26–32 wt% calcium carbonate or talc filler, 1–3 wt% naphthenic process oil, and the balance oxidized bitumen with a softening point of 90–110 °C. The SBS network is not used as the primary modifier in APP-dominated membrane systems; blending SBS 1484 with atactic polypropylene above 5 wt% produces separate phases and unstable softening-point measurements.

    SBS 1484 (wt%)Filler (wt%)Softening point (°C, ASTM D36-14)Low-temperature flexibility (°C, EN 1109:2013)Elastic recovery (%, ASTM D6084-18)
    832108-555
    1030116-1065
    1228124-1575
    1426132-2082

    Downstream processing of the mixed compound is carried out on a heated doctor-blade or three-roll calender line at 1.0–1.5 m/min; the compound is coated onto polyester or glass-fiber reinforcement at 170–180 °C, then surfaced with sand, talc or polyethylene film. Terminal product types include torch-applied SBS-modified bitumen cap sheets, self-adhered SBS-bitumen base sheets, and bridge-deck waterproofing membranes in 4 mm and 5 mm nominal thicknesses.

    What Governs Viscosity Stability in SBS 1484 Hot-Melt Pressure-Sensitive Adhesives?

    Brookfield viscosity at 160 °C for SBS 1484 hot-melt pressure-sensitive adhesives typically lies between 11,000 mPa·s and 22,000 mPa·s when the elastomer content is increased from 20 wt% to 35 wt%. The viscosity window is selected to balance coat-weight stability and adhesive transfer; below 12,000 mPa·s, slot-die coat-weight control becomes unstable above 200 m/min, while above 25,000 mPa·s the gear-pump inlet pressure at the coating head can exceed 2.0 MPa. Batch preparation is conducted in a heated sigma-blade mixer with 80–120 kg working capacity at 150–165 °C under nitrogen flow of 2–4 m³/h. Naphthenic oil and hindered phenol antioxidant are charged first, followed by SBS 1484 crumb, and then C5 tackifier is added incrementally over 20–30 min to prevent torque overload. A finished melt after 60 min is visually clear and free of undispersed crumb; the mixer wall temperature is not permitted to exceed 170 °C because the unsaturated butadiene midblock undergoes shear-induced thermal degradation at prolonged residence times.

    Regulatory compliance for food-contact tape and label applications is assessed under 21 CFR 175.105 as an indirect food additive; electrical and electronic accessory adhesives may require halogen-content documentation aligned with IEC 61249-2-21, and REACH Annex XVII restrictions apply to polycyclic aromatic hydrocarbons in consumer articles. The addition ratio for SBS 1484 in the final adhesive is 20–35 wt%, with tackifier at 34–44 wt%, naphthenic oil at 30–35 wt%, and antioxidant at 0.5–1.0 wt%.

    SBS 1484 (wt%)C5 tackifier (wt%)Naphthenic oil (wt%)Melt viscosity at 160 °C (mPa·s, ASTM D3236-88)Loop tack (N/25 mm, ASTM D6196-23)Shear adhesion failure time (h, ASTM D3654/D3654M-22)
    204435.511,00094
    253935.514,500128
    303435.518,0001515
    352935.522,0001825

    Coating lines apply the hot-melt with a narrow-slot die at 150–170 °C; for double-sided tape, coat weight is 15–25 g/m² on PET release liner, while carton-sealing tape uses direct coating on polypropylene film at 25–35 g/m². Accelerated QUV exposure under ASTM G154-16 is required for outdoor tape formulations; without carbon black or UV stabilizer, surface tack loss appears within 200 h in SBS 1484 systems. Terminal product types include pressure-sensitive carton-sealing tapes, label stocks for glass and PET containers, hygiene construction adhesives for diaper waistband positioning, and transfer films for low-surface-energy bonding.

    When SBS 1484 is sheared into paving-grade bitumen at 4.5 wt%, the dispersed polymer-particle size is reduced below 10 µm after 45–60 min in a colloid mill operating at 3,000 rpm. The binder is held at 180–190 °C during high-shear dispersion and then stirred at low agitation for 60–90 min to complete swelling. The critical process threshold is storage stability: without a stabilizer, a 3-day hot-storage test at 163 °C can produce a softening-point difference between the top and bottom of the sample exceeding 5 °C under ASTM D36-14. Elemental sulfur added at 0.1–0.3 wt% of binder reduces the difference to below 2 °C by lightly crosslinking the butadiene midblock; sulfur above 0.4 wt% can generate non-homogeneous gel structures and reduce low-temperature ductility.

    Compliance for polymer-modified paving binders is specified by EN 14023:2010 and AASHTO M332-22; performance-graded testing follows ASTM D6373-21 for dynamic shear rheometry, ASTM D6084-18 for elastic recovery, and ASTM D7405-20 for multiple stress creep recovery. The addition ratio range for SBS 1484 in paving bitumen is 3.5–5.5 wt%, with 4.0–4.5 wt% common for PG 70-22 and 5.0–5.5 wt% for PG 76-22 depending on aromatic content of the base bitumen.

    Downstream terminal product types are PG 70-22, PG 76-22, and PG 76-28 polymer-modified bitumen binders for highways, bridge decks, airport aprons, and intersection pavements with slow-moving heavy-vehicle loading.

    If the Barrel Zone Profile Is Flattened Below 175°C in TPR Compounding

    Injection-molded TPR outsoles produced from SBS 1484 require a compounding melt temperature above 175 °C, but the die temperature is controlled at 190–200 °C because the butadiene block undergoes thermo-oxidative chain scission during extended residence above 210 °C. A co-rotating twin-screw extruder with L/D 36:1 uses a barrel sequence of 160/175/185/190/195 °C and screw speed of 300–350 rpm to disperse 20–25 wt% GPPS and 0–15 wt% silica or calcium carbonate into the SBS matrix. The formulation addition ratio is 30–45 wt% SBS 1484, 20–25 wt% GPPS, 10–20 wt% naphthenic oil, 0–15 wt% filler, 0.2–0.5 phr antioxidant, and 0.3–0.5 phr zinc stearate. Injection molding uses a two-cavity outsole tool with clamp force 800–1,200 kN, melt temperature 170–190 °C, mold temperature 25–35 °C, and holding pressure 30–50 MPa.

    Compliance testing uses ISO 37:2017 for tensile stress-strain, ISO 868:2003 for Shore A hardness, and ISO 4649:2017 for abrasion; footwear articles must also satisfy REACH Annex XVII polycyclic aromatic hydrocarbon limits and, where applicable, RoHS 2011/65/EU for electronic foot-care devices. SBS 1484 compounds are not recommended for applications requiring abrasion loss below 150 mm³ under ISO 4649:2017 or oil resistance under ASTM D471-16a, because the butadiene segment is incompatible with high-aromatic oils and abrasive surfaces cause high wear at the outer sole.

    Terminal product types include injection-molded casual footwear outsoles, unit soles for slippers, anti-slip pads, and skate-wheel outer layers.

    GPPS Sheet Extrusion Loading Constraints and Cold-Roll Orientation

    Blending 8 wt% SBS 1484 into general-purpose polystyrene sheet extrusion resists impact crack propagation but increases haze from approximately 1–2% to 8–12% depending on sheet thickness; clarity-sensitive packaging therefore operates at the lower end of the 5–10 wt% range. Published data for this specific GPPS/SBS 1484 configuration is limited, so plant trials should validate sheet gauge control and thermoforming uniformity before production release. Compounding is performed on a tightly intermeshing twin-screw extruder with L/D 40:1, barrel temperatures 200–220 °C, and a gear pump to damp pressure variation; the melt is extruded through a flat die into a three-roll cold-roll stack at 60–80 °C. The addition ratio for SBS 1484 is 5–15 wt%.

    Food-contact sheet produced from the blend requires compliance with 21 CFR 177.1640 for polystyrene and, for SBS as an impact modifier, documentation under 21 CFR 177.1810 or EU Regulation 10/2011 with migration testing for total hydrocarbons. Terminal product types are extruded clamshell packaging, food trays, cosmetic blisters, and non-sterile medical packaging trays.

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    Certification & Compliance
    More Introduction

    LCY Chemical Globalprene® SBS 1484 is a linear styrene-butadiene-styrene block copolymer supplied as porous pellets. It is manufactured by sequential anionic polymerization, producing a two-phase morphology with polystyrene end-blocks and an unsaturated polybutadiene midblock. Bound styrene content is approximately 31 wt%. The grade is supplied without extender oil, which distinguishes it from oil-extended SBS grades containing 30–50 phr paraffinic or naphthenic process oil and therefore exhibiting lower hardness and higher melt flow at equivalent molecular weight. Relative to styrene-isoprene-styrene copolymers, 1484 exhibits higher room-temperature tensile strength and abrasion resistance but lower hot-melt tack. Relative to hydrogenated styrene-ethylene/butylene-styrene copolymers, it has a lower continuous service temperature ceiling because the unsaturated butadiene midblock is not hydrogenated. Compared with radial SBS polymers, the linear architecture of 1484 generally produces lower die swell and reduced melt elasticity at equivalent bound styrene content, which can improve dimensional stability in injection-molded and extruded articles.

    PropertyTypical valueTest method
    Bound styrene content31 wt%ISO 2453
    Volatile matter≤0.5 wt%ASTM D5668
    Ash≤0.2 wt%ASTM D5663
    Melt mass-flow rate4.0–6.0 g/10 minASTM D1238 at 190°C, 5 kg
    Tensile strength at break≥18.0 MPaISO 37
    Elongation at break≥700%ISO 37
    Modulus at 300% elongation≥2.0 MPaISO 37
    Hardness70 Shore AISO 48-4
    Specific gravity0.94ISO 1183

    When 1484 Replaces Oil-Extended SBS in Microcellular Footwear Soles

    When 1484 is selected for microcellular shoe sole compounds, the absence of extender oil shifts formulation latitude toward higher plasticizer loadings without exceeding target hardness. A typical lightweight sole formulation includes 100 phr of 1484, 20–40 phr of circulation oil, 5–15 phr of general-purpose polystyrene, 0.5–2.0 phr of azodicarbonamide blowing agent, and 1.5–3.0 phr of dicumyl peroxide. On an injection-molding machine with clamp force of 1500 kN and a 20:1 L/D three-zone screw, barrel temperatures are set from 150°C to 175°C, and the nozzle is held below 185°C. Melt temperatures above 220°C trigger thermal-oxidative degradation of the polybutadiene midblock, producing gel particles, surface roughness, and loss of tear strength. The blowing gas evolves from the azodicarbonamide decomposition range of 150–200°C; if first-stage temperature is too low, melt viscosity remains too high for uniform cell nucleation, while excessive second-stage temperature causes cell coalescence and surface collapse. Batch-to-batch variation in melt mass-flow rate should be controlled to within ±0.5 g/10 min for consistent shot size and foam density. Capillary rheometry at 160°C and apparent shear rates of 100–1000 s⁻¹ is used to detect viscosity drift before production campaigns.

    Melt blending of 1484 into general-purpose polystyrene at 5–15 wt% increases notched impact resistance without large reductions in tensile modulus. Twin-screw extruders with 40:1 L/D and downstream feeding of 1484 into melted polystyrene are used to limit butadiene thermal history. The dispersed SBS domain size is maintained below 1.0 μm; larger domains reduce transparency and lower impact efficiency. Charpy impact is measured by ISO 179-1, and tensile properties by ISO 527-1. Compared with polybutadiene rubber impact modifiers, SBS contributes higher styrene compatibility and easier dispersion because the styrene end-blocks interact with the polystyrene matrix. The unsaturated midblock requires stabilization because extrusion above 230°C can cause gel formation and surface streaks.

    Bituminous binder modification using Globalprene® SBS 1484 is conducted at 170–185°C under high-shear dispersion using a rotor-stator homogenizer. The polymer is typically added at 4–6 wt% of binder mass, and dispersion continues for 45–90 min until swelling and phase inversion produce a polymer-rich network. Softening point is measured by ASTM D36, penetration by ASTM D5, and storage stability by ASTM D7173. The difference between SBS-modified binders and reactive thermoplastic elastomers is that the SBS network is physical, not chemical; the polystyrene end-blocks associate into glassy domains below 100°C, while the polybutadiene midblocks provide elastic recovery at asphalt service temperatures. Sulfur crosslinking at 0.5–1.5 wt% is sometimes applied to reduce phase separation and improve softening point, but the addition window is narrow because sulfur doses above 2.0 wt% can produce gelled binder and viscosity peaks exceeding mixing capacity. Published data for this specific configuration is limited, and field validation should be conducted on the project bitumen source because aromaticity and asphaltene content govern swelling kinetics.

    Which Melt Processing Limits Apply on Twin-Screw Compounding Lines?

    Compounding of 1484 on a co-rotating twin-screw extruder with 40:1 L/D and 25–40 mm screw diameter is typically performed with a barrel profile of 160/170/175/180/185°C and die temperature of 185°C. Screw speed is held at 250–350 rpm, and specific mechanical energy input is maintained between 0.18 kWh/kg and 0.25 kWh/kg. A side feeder is used for mineral fillers above 20 phr to avoid barrel wear and melt temperature spikes. The polymer is pre-blended with polystyrene or other hard-phase modifiers before the main feed throat; direct feeding of neat 1484 pellets without pre-blending can produce screw surging when volumetric feeders interact with porous pellet bulk density variation. Strand die-face temperatures above 190°C cause strand tack and pelletizer jamming, observed as double pelts and melt wrap on the cooling belt. Vent ports are configured with atmospheric venting in zone 4 and vacuum venting at −0.06 MPa in zone 7 to strip residual moisture and low-molecular-weight volatiles. For pre-drying, pellets stored above 60% relative humidity are dried at 70°C for 2 h; conventional hot-air drying is sufficient.

    For solvent-borne adhesive compounding, a toluene solution of 1484 at 25 wt% solids shows pseudoplastic flow with a Brookfield viscosity in the range of 300–800 mPa·s at 25°C, depending on residual moisture and toluene purity. Hydrogenated rosin ester tackifier added at 40–60 phr raises loop tack while reducing cohesive shear; a hindered phenolic antioxidant at 0.1–0.3 wt% delays midblock oxidation during hot-melt processing. Coating weights of 20–40 g/m² on polyester film are used for pressure-sensitive adhesive tapes; peel adhesion is evaluated by ASTM D3330 and shear adhesion by ASTM D3654. Lower solution viscosity than high-molecular-weight radial grades improves coating line speed on comma-coating and slot-die coating lines. The unsaturated midblock can react with ozone, so adhesive products are formulated with microcrystalline wax and antiozonants when long-term exterior exposure is required.

    Regulatory Compliance Matrix and Application Boundaries

    Regulatory or quality referenceScopeCondition
    REACH (EC) 1907/2006EU chemical registrationSupplier declaration required; SVHC content below 0.1 wt% per batch certificate
    RoHS 2011/65/EUElectrical and electronic equipmentCompliance declared for lead, mercury, cadmium, hexavalent chromium, PBB, PBDE below directive limits
    ISO 9001:2015Quality managementProduction site certification must be verified by current certificate
    FDA 21 CFR 177.1810Styrene block copolymers in repeated-use food contactApplicable only under specific end-use conditions with supplier migration testing
    ASTM D1238, ASTM D638, ASTM D2240Melt flow, tensile, hardnessBatch certificate values control acceptance

    Compliance with the listed standards applies only to material supplied under standard commercial specifications; batch-specific certificates of analysis control the values in Table 1. Food-contact acceptance under 21 CFR 177.1810 is use-limited and requires migration testing under end-use conditions; it is not an unconditional clearance.

    Operational boundaries require attention to oxidative stability and solvent compatibility. The unsaturated polybutadiene midblock is sensitive to prolonged exposure above 220°C, ozone, and ultraviolet radiation; compounds without antidegradants develop surface cracking under accelerated weathering by ASTM G154 within 200–400 h. Ketone and ester solvents induce swelling; aliphatic hydrocarbon solvents with solubility parameters of 7.0–8.0 (cal/cm³)^0.5 provide stable viscosities. Strong oxidizing agents and concentrated nitric acid are incompatible. The product should not be blended with high-acid-number bitumens above 200°C for more than 2 h because asphalt oxidation and polymer chain scission can produce viscosity regression. Scrap rates on injection-molding lines increase when regrind content exceeds 20 wt% unless antioxidant levels are adjusted to compensate for thermal history. Published data for this specific configuration is limited; plant trial validation under production thermal history remains required for applications at the upper melt-temperature boundary.

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