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LCY Chemical Globalprene® SBS 3545

    • Product Name: LCY Chemical Globalprene® SBS 3545
    • 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 139963
    Productname LCY Chemical Globalprene® SBS 3545
    Chemicaltype Styrene-butadiene-styrene block copolymer (SBS)
    Blockstructure Linear
    Styrenecontent 45 wt% (typical)
    Butadienecontent 55 wt% (typical)
    Density 0.94–0.96 g/cm³
    Meltflowrate 3 g/10 min (200°C/5 kg, typical)
    Shoreahardness 90 (typical)
    Tensilestrength 20–25 MPa
    Elongationatbreak 600–700%
    Volatilematter ≤0.5 wt%
    Ashcontent ≤0.2 wt%
    Appearance White to off-white pellets
    Packaging 25 kg bags

    As an accredited LCY Chemical Globalprene® SBS 3545 factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing LCY Chemical Globalprene® SBS 3545 packaging: 25 kg bags, palletized for safe industrial handling and storage.
    Container Loading (20′ FCL) 20′ FCL dry container loaded with LCY Chemical Globalprene® SBS 3545, properly stowed and secured for ocean transport.
    Shipping LCY Chemical Globalprene® SBS 3545 is a non-hazardous styrene-butadiene-styrene block copolymer thermoplastic elastomer. It is shipped in moisture-proof packaging and is not classified as dangerous goods for transport. Store dry, cool, ventilated, away from direct sunlight and ignition sources.
    Storage Store LCY Chemical Globalprene® SBS 3545 in a cool, dry, well-ventilated warehouse, away from direct sunlight, heat, and ignition sources. Keep original packaging sealed and protect from moisture, contamination, and prolonged high temperatures. Avoid heavy stacking that may deform the product, follow first-in, first-out rotation, and keep away from strong oxidizers and acids.
    Shelf Life Typically 24 months from production when stored in original packaging under cool, dry, well-ventilated conditions, away from direct sunlight and heat.
    Application of LCY Chemical Globalprene® SBS 3545

    In polymer-modified bitumen for dense-graded road pavements, Globalprene® SBS 3545 is metered into hot base bitumen at a dosing rate of 3.0–5.5 wt% based on neat binder mass, while open-graded friction courses and stress-absorbing membrane interlayers are formulated at 5.0–7.5 wt% to force phase inversion into a continuous polymer-rich network. The 35 wt% bound styrene block content provides room-temperature physical crosslinks that raise ring-and-ball softening point from 45–52 °C to a modified range of 65–85 °C when tested in accordance with ASTM D36; elastic recovery measured under ASTM D6084 is retained at or above 60% at 25 °C only when the polymer has been dispersed into the maltene phase with adequate shear. Base binder quality is controlled to EN 12591, and the finished polymer-modified bitumen is evaluated under EN 14023 and AASHTO M320; short-term oxidative aging is simulated by ASTM D2872 at 163 °C for 5 h or by EN 14769 for the rotating flask method. Production-scale dispersion is carried out in hot-oil jacketed horizontal tanks fitted with dual-shaft high-shear dispersers of 30–75 kW or inline rotor-stator mills with tip speeds of 15–25 m/s; the bitumen is preheated to 170 °C before polymer addition, held at 175–185 °C during high-shear mixing, and then transferred to maturation tanks with low-speed agitation for 2–4 h. Temperature excursions above 200 °C in the presence of atmospheric oxygen initiate chain scission in the polybutadiene midblock and shorten the 5 °C ductility response of the final binder; therefore, the recirculation loop is sized for 20–60 m³/h throughput to limit residence time at high temperature and avoid gel particle accumulation on heat exchangers. Terminal product types include polymer-modified binders for dense-graded asphalt concrete, open-graded friction courses, airport runway overlays, bridge deck waterproofing courses, and stress-absorbing membrane interlayers used over cracked concrete pavements.

    Phase-inversion behavior in this application is not fixed by polymer dosage alone; it shifts with the maltene fraction of the base bitumen and the aromatic oil concentration. With paraffinic or low-aromatic bitumen, the same 5.0 wt% SBS charge can produce a coarse, unstable morphology that separates during storage, whereas a bitumen with 55–65% maltenes and 5–10% aromatic process oil develops an interlocking SBS network that remains stable under 72 h storage at 160 °C without visible skinning. Plant-scale batch records show that separation is detectable as a top-layer viscosity increase of more than 20% after 72 h when dispersion has been insufficient, which can be corrected by increasing mixer tip speed above 18 m/s or extending high-shear time by 15–30 min. Published data for this specific configuration is limited to binder suppliers’ compatibility charts, so process validation under the customer’s base bitumen source remains mandatory.

    Bituminous waterproofing membrane compounds where 3545 modifies low-temperature flex resistance

    Bituminous cap sheet and torch-applied membrane compounds formulated with Globalprene® SBS 3545 are charged at 8–14 wt% based on total compound weight, combined with 20–40 wt% slate dust or dolomite filler, 2–6 wt% aromatic process oil, and a stabilizer package at 0.2–0.5 phr to protect against autoxidation during prolonged hot storage. Mixing is carried out in jacketed sigma-blade mixers or continuous twin-screw extruders with L/D ratios between 30:1 and 48:1; the polymer and bitumen are pre-blended at 150–170 °C, filler is added after the polymer has formed a continuous phase, and the finished compound is calendered or flood-coated onto a polyester nonwoven or glass fleece carrier at 100–140 °C. Compliance for factory-made reinforced bitumen sheets is governed by EN 13707, with American formulations tested to ASTM D6164/D6164M for SBS-modified bituminous sheet materials, ASTM D5147 for sampling and testing, and ASTM D2523 for low-temperature flexibility; grades are typically certified to -25 °C or -40 °C cold bend performance on a 150 mm mandrel. The 10 wt% addition level is a practical balance point for cap sheets because it raises cold flex crack resistance without increasing compound viscosity beyond the pump capacity of standard calender feed systems. Terminal products include torch-on waterproofing membranes for below-grade foundations, self-adhesive roofing underlayments, bridge deck membranes, and basement tanking systems where the finished sheet must retain flexibility at sub-zero temperatures after UV exposure of the upper bituminous layer.

    Melt processing of injection-grade footwear soles and unit bottoms based on Globalprene® SBS 3545 begins with a formulation of 100 phr SBS, 20–40 phr general-purpose polystyrene to raise scuff resistance and dimensional stability, 20–60 phr naphthenic oil to control Shore hardness and melt flow, 0–30 phr calcium carbonate to reduce formulation cost, and a stabilizer system of 0.1–0.5 phr phenolic antioxidant plus 0.1–0.3 phr phosphite co-stabilizer. The compound is first produced on a co-rotating twin-screw extruder with a screw length-to-diameter ratio of 44:1, screw speed 350–550 rpm, and barrel temperature profile from 130 °C near the feed throat to 165 °C at the die; the strand is water-ring pelletized and dried to a moisture content below 0.05 wt% before injection molding. Molding is performed on reciprocating-screw injection machines with clamp force between 1,000 and 3,000 kN, shot sizes held at 60–80% of barrel capacity, nozzle temperatures maintained at 150–170 °C, and mold temperatures at 20–50 °C to promote rapid solidification of the styrene domains. A narrow processing window of roughly ±5 °C at the nozzle exists because stock temperature above 180 °C accelerates gel formation in the polybutadiene midblock, while temperatures below 145 °C can produce delamination at the mold fill front. Compliance for footwear compounds includes REACH SVHC content declarations and California Proposition 65 screening, with physical properties tested by ASTM D2240 for Shore A hardness, ISO 37:2024 for tensile strength and elongation, ISO 34-1:2022 for tear strength, and ISO 4649 for abrasion loss. Terminal product types include injection-molded soles for casual and safety footwear, solid and expanded unit bottoms, slip-resistant outsoles, and insert foams produced with chemical blowing agents at 0.5–1.5 phr in the same SBS matrix.

    What limits hot-melt viscosity stability in SBS-based pressure-sensitive adhesives?

    Hot-melt pressure-sensitive adhesive formulations containing Globalprene® SBS 3545 are compounded at 15–25 wt% polymer, 40–60 wt% C5/C9 aliphatic-aromatic tackifying resin, 10–25 wt% naphthenic or white mineral oil, and 0.3–1.0 phr antioxidant system. The polymer is charged first into a jacketed sigma-blade mixer or high-torque twin-screw extruder at 140–160 °C under a nitrogen blanket with residual oxygen below 0.5 vol%; tackifier resin is introduced after the polymer reaches a uniform melt to avoid localized viscosity spikes at the feed throat, and oil is metered last to reach a Brookfield viscosity of 3,000–50,000 mPa·s at 150 °C, depending on the target coating method. Viscosity stability during 24 h aging at 150 °C is assessed by ASTM D4499; change beyond ±15% generally indicates polybutadiene block degradation or tackifier oxidation rather than simple phase separation and requires reformulation of the antioxidant package or a reduction of the peak mixer temperature. Compliance for pressure-sensitive adhesive applications includes FDA 21 CFR 175.105 for indirect food contact, REACH SVHC screening, RoHS 2011/65/EU for electrical tape, ASTM D3330 for peel adhesion, and PSTC-16 for loop tack. Slot-die coating at 120–140 °C onto polyethylene terephthalate or polypropylene film produces a uniform adhesive layer; slot gap is typically 0.25–0.50 mm, and line speed is limited by the hot melt’s cohesive strength. Terminal products include carton-sealing tapes, label stocks, hygiene attachment strips, and diaper closure tapes.

    Thermal history is the dominant process variable in this sector because SBS 3545 begins to lose unsaturated polybutadiene integrity above 180 °C; a mixer setpoint of 150 °C may still produce localized wall temperatures above 175 °C if oil is not preheated or if the tackifier charge is delivered too quickly. Production-scale sigma-blade mixers with 500–1,500 L capacities are typically fitted with scraped-wall agitators and jacket pressure not exceeding 0.4 MPa saturated steam; direct steam injection is avoided because it introduces moisture and accelerates ester hydrolysis in some tackifier resins. The finished adhesive is filtered through 100–150 µm mesh before slot-die coating to remove gel bodies, which otherwise appear as coating streaks on polyethylene terephthalate film.

    Application sectorPrimary compliance standardsCritical test conditionQuantitative reference
    Polymer-modified bitumenEN 14023, AASHTO M320, ASTM D6084Elastic recovery at 25 °C60% minimum
    Waterproofing membranesEN 13707, ASTM D6164, ASTM D2523Cold bend at -25 °C150 mm mandrel
    Footwear solingISO 37:2024, ISO 34-1:2022, ISO 4649Physical property testing at 23 °Cgrade-specific
    Hot-melt PSAFDA 21 CFR 175.105, ASTM D3330, PSTC-16Viscosity stability 24 h at 150 °C±15% change
    Polypropylene modificationISO 180:2023, ISO 178:2019, RoHS 2011/65/EUNotched impact at -20 °C15 kJ/m²
    Sealants/masticsASTM C920, ISO 8339:2019, ISO 7389Tensile adhesion at -20 °Csubstrate-dependent

    Polypropylene impact modification and co-continuous morphology control

    At addition levels of 5–20 wt% in polypropylene, Globalprene® SBS 3545 is dispersed on twin-screw extruders with L/D ratio 48:1, screw speed of 400–600 rpm, and barrel temperatures from 180 °C to 210 °C. The SBS phase functions as a dispersed impact modifier; at 10–15 wt%, it raises Izod notched impact strength at -20 °C from below 5 kJ/m² to above 15 kJ/m² when tested by ISO 180:2023, while flexural modulus measured by ISO 178:2019 remains above 900 MPa if filler loading is kept below 10 wt%. Morphology control is achieved by maintaining the polypropylene matrix melt temperature above 170 °C and below 220 °C; the lower boundary ensures sufficient matrix viscosity for droplet breakup, while the upper boundary avoids thermo-oxidative chain scission of the polybutadiene segments and the resulting emission of low-molecular-weight hydrocarbon volatiles. The target dispersed elastomer domain size is below 2 µm; larger domains indicate insufficient shear or poor melt viscosity matching and correspond to inconsistent low-temperature impact performance. Compliance includes REACH and RoHS 2011/65/EU for electrical and electronic components; mechanical testing follows ISO 179-1:2023 for Charpy notched impact, ASTM D3763-24 for instrumented puncture, and ISO 75-2:2020 for heat deflection temperature. Terminal products include soft-touch appliance housings, automotive interior door panel inserts, low-noise conveyor components, and impact-modified packaging for refrigerated distribution.

    At the upper addition level of 20 wt%, the co-continuous phase structure can reduce heat deflection temperature below 70 °C under ISO 75-2:2020 method A if the SBS phase is not selectively crosslinked or if the crystallinity of the PP continuous phase is depressed by oil migration from the elastomer. Injection molders report that soft-touch parts with wall thickness below 2 mm are prone to sink marks unless hold pressure is increased to 50–70 MPa and melt cushion is maintained at 3–5 mm. Those dimensional control measures are specific to SBS-modified PP and differ from polyolefin elastomer systems because the styrene domains of SBS 3545 solidify faster at the sudden temperature drop in the mold cavity.

    When high-temperature compression set rules out polyolefin elastomers

    Construction sealant and mastic systems based on Globalprene® SBS 3545 are solvent-borne or high-solids compounds with 10–20 wt% polymer based on total wet compound, 20–40 wt% aromatic hydrocarbon resin, 10–30 wt% calcium carbonate or kaolin filler, and 0.3–0.8 phr antioxidant. Manufacturing is carried out in low-speed planetary dispersers with stainless steel vessels, scraped-wall clearances below 0.5 mm, and two-stage solvent addition; the first stage maintains a paste viscosity of 200,000–500,000 mPa·s during pigment wetting and polymer dissolution, while the second stage reduces the final trowel-grade viscosity to 50,000–120,000 mPa·s. The cured film is tested to ISO 8339:2019 for tensile adhesion with movement limits at -20 °C, ISO 7389 for low-temperature flexibility, and ASTM C920 for cold-applied elastomeric joint sealants; adhesion strength after extension is typically not reported without specifying the substrate and primer system. Operational boundaries include maintaining solvent vapor concentrations below 25% of the lower explosive limit, isolating the mixer from ignition sources, and avoiding amine-based adhesion promoters because they catalyze oxidative degradation of the polybutadiene midblock and can darken the sealant during storage. Terminal products include high-movement construction joint sealants, automotive seam sealants, and vibration damping mastics where the SBS phase provides elastic recovery without the high-temperature processing requirements of vulcanized rubber.

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    Certification & Compliance
    More Introduction

    LCY Chemical Globalprene® SBS 3545 is introduced as a linear styrene-butadiene-styrene block copolymer supplied in porous pellet form for melt compounding, solution processing, and bitumen modification. Manufacturer-published typical values place bound styrene at 45 wt%, specific gravity at 0.94 under ASTM D792-20, and melt flow rate at 5 g/10 min under 200°C and 5 kg load using ASTM D1238-20. Tensile strength at break is reported at 25.0 MPa with elongation at break of 700% when tested according to ASTM D638-14, while Shore A hardness is reported at 90 under ISO 868:2003. The grade is therefore positioned between lower-styrene, bitumen-compatible SBS grades and higher-styrene, high-hardness styrenic molding grades. Its linear triblock architecture provides re-meltability and physical crosslinking at service temperature, but the unsaturated polybutadiene midblock requires specific thermal and oxidative stabilization during compounding.

    What Molecular Parameters Govern the Processing and Mechanical Response of SBS 3545?

    The molecular architecture consists of polystyrene end blocks separated by a polybutadiene midblock. Differential scanning calorimetry under ISO 11357-2:2020 identifies a polystyrene domain glass transition near 95°C and a polybutadiene midblock glass transition below −80°C for this class of block copolymer. Below the polystyrene glass transition, the end blocks form glassy domains that act as physical crosslinks; above 100°C, those domains soften and permit thermoplastic flow. The 45 wt% bound styrene content produces a higher crosslink-domain volume fraction than low-styrene SBS grades, which increases tensile strength, hardness, and resistance to cold flow, but reduces compatibility with low-aromatic hydrocarbon phases.

    On a co-rotating twin-screw extruder with 32:1 L/D and screw speed of 250–350 rpm, melt temperature is typically managed between 170°C and 190°C. Apparent viscosity decreases with increasing shear rate in capillary rheometry, a non-Newtonian response that supports screw plastication but also creates viscous dissipation. Processors must therefore avoid extended residence time above 220°C, where the unsaturated butadiene segment undergoes chain scission and crosslinking that appears as gel particles or surface roughness. Melt viscosity at low shear is higher than that of oil-extended SBS grades, but the narrow molecular weight distribution of the linear architecture yields predictable injection and extrusion behavior when the plastication zone is maintained within the specified range.

    Bitumen modification with SBS 3545 is typically performed on production-scale high-shear mills operating at rotor tip speeds of 3,000–5,000 rpm, followed by low-shear maturation at 170–185°C. Addition levels between 3 wt% and 6 wt% based on base bitumen are common for paving-grade binders, while polymer-modified asphalt for waterproofing membranes may require 8–12 wt%. The dispersion mechanism depends on swelling of the polybutadiene midblock by maltene fractions and formation of a continuous polymer-rich network. Insufficient mixing yields gel-like polymer-rich specks; excessive shear at temperatures above 200°C accelerates oxidative degradation of the unsaturated midblock. Quality control on plant batches uses ASTM D5 penetration at 25°C, ASTM D36 ring-and-ball softening point, ASTM D6084 elastic recovery at 25°C, and EN 13399 storage-stability cork tube testing. A storage-stable blend typically exhibits a softening-point difference of no more than 2.5°C between top and bottom sections after 72 h at 180°C; published data for a specific base bitumen is required because aromatic and asphaltene content shifts the compatibility boundary. Paving trials additionally evaluate performance-grade parameters through ASTM D7175 dynamic shear rheometry and ASTM D6648 bending beam rheometer low-temperature stiffness.

    Adhesive, Sealant, and Shoe Sole Molding Windows

    In hot-melt and solvent-borne adhesive formulations, SBS 3545 is compounded with aliphatic or naphthenic process oils and hydrogenated tackifier resins. The styrenic end-blocks require controlled aromatic content in the tackifier package to balance peel and shear; excessive aromatic resin plasticizes the polystyrene domains and reduces cohesive strength. Formulation screening uses ASTM D903-98(2024) for 180° peel adhesion and ASTM D3654/D3654M-06(2019) for shear adhesion failure temperature. Published comparative data for this grade in fully formulated adhesives remains limited; therefore, laboratory trials are required to fix tackifier loading between 80 phr and 150 phr per hundred rubber. In shoe sole injection molding, barrel zone settings from 160°C to 190°C and mold temperatures of 20–40°C are used on conventional reciprocating-screw equipment. Holding pressure between 40 MPa and 70 MPa is typical to compensate for shrinkage; cycle time is governed by the concentration-driven solidification of styrenic domains rather than crystallization.

    Compared with lower-styrene SBS grades carrying approximately 30 wt% bound styrene, SBS 3545 produces higher tensile strength, higher Shore A hardness, and better resistance to flow at elevated pavement temperatures. The lower-styrene grades disperse more readily in low-aromatic bitumen and produce softer compounds, but they exhibit lower cohesive strength and lower upper service modulus. Compared with higher-molecular-weight or coupled SBS grades, SBS 3545 is described as a linear, medium melt-flow product; it retains melt processability in injection molding but may show lower extensional viscosity in blow molding or sheet extrusion. Against random styrene-butadiene rubber, the block sequence restricts flow at service temperature and creates true thermoplastic re-meltability. Against hydrogenated SEBS grades, SBS 3545 carries unsaturated midblock double bonds, giving lower oxidative and ultraviolet stability but often lower melt viscosity at equivalent composition and higher permeability in dense rubber compounds.

    When Polystyrene Impact Modification Uses SBS 3545 at Loading Thresholds Above 10 wt%

    Compounding SBS 3545 into general-purpose polystyrene is performed at 10–20 wt% rubber content by twin-screw extrusion with downstream melt devolatilization. Notched Izod impact values measured under ASTM D256-23 increase as rubber particle morphology develops, while tensile modulus measured under ASTM D638-14 declines in proportion to rubber volume fraction. The process conflict is that higher screw speeds improve dispersion but reduce residence time; if the melt temperature exceeds 220°C, the unsaturated butadiene segments generate gel particles and surface defects. Published data for this specific grade in polystyrene at 15 wt% loading is limited; production trials on 25:1 L/D twin-screw extruders have been reported with barrel temperatures from 170°C to 200°C and zone-specific vacuum venting at −0.06 MPa. The same technology is applied in modification of polyolefin compounds, but compatibility with isotactic polypropylene is limited without an interfacial agent.

    Thermal-oxidative stabilization of SBS 3545 must account for the polybutadiene midblock. Unstabilized crumb exposed to air at storage temperatures above 40°C can undergo viscosity rise and gel formation within 30–90 days; published data for this specific grade is limited, and storage stability should be verified by melt flow rate retention under ASTM D1238-20. The use of phenolic primary antioxidants at 0.1–0.4 phr and phosphite secondary antioxidants at 0.1–0.3 phr is standard practice in compounding. The product should not be combined with strong oxidizing agents, concentrated copper-containing heat stabilizers, or amine-based curatives designed for nitrile rubbers; such combinations accelerate radical degradation or alter the termination chemistry. Pre-drying before melt processing is required when moisture content exceeds 0.1 wt%; typical drying conditions are 70–80°C for 2–4 h in a desiccant dryer with dew point below −30°C. Extrusion vent ports should be placed in the devolatilization zone and maintained under vacuum to remove adsorbed moisture and low-molecular-weight volatiles.

    Compliance Verification Is Conducted Against the Following Designation Matrix

    PropertyTypical ValueTest Designation
    Bound styrene45 wt%Manufacturer internal method
    Specific gravity0.94ASTM D792-20
    Melt flow rate5 g/10 min at 200°C/5 kgASTM D1238-20
    Tensile strength at break25.0 MPaASTM D638-14
    Elongation at break700%ASTM D638-14
    Shore A hardness90ISO 868:2003
    Asphalt elastic recoveryReported on modified binderASTM D6084
    Bitumen storage stabilityReported on modified binderEN 13399

    For full compliance submissions, the material safety data sheet and REACH registration documents remain the controlling references; the table above is a screening matrix and does not replace batch-specific certificates of analysis.

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