| HS Code | 671722 |
| Polymer Type | Styrene-butadiene-styrene (SBS) block copolymer |
| Block Structure | Linear |
| Styrene Content | 45 wt% |
| Density | 0.95 g/cm3 |
| Melt Flow Rate | 6.0 g/10 min (200°C, 5 kg) |
| Shore A Hardness | 75 |
| Tensile Strength | 25 MPa |
| Elongation At Break | 700% |
| 300 Modulus | 5.0 MPa |
| Volatile Matter | ≤0.5 wt% |
| Ash Content | ≤0.2 wt% |
| Solution Viscosity | 800 mPa·s (25 wt% in toluene, 25°C) |
| Appearance | White to off-white pellets/crumb |
As an accredited LCY Chemical Huizhou Globalprene® SBS 3546 factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | LCY Chemical Huizhou Globalprene® SBS 3546 is supplied in 25 kg moisture-barrier paper bags, palletized for bulk transport. |
| Container Loading (20′ FCL) | LCY Chemical Huizhou Globalprene® SBS 3546 is loaded in a 20′ FCL container under dry conditions, securely palletized and shrink-wrapped. |
| Shipping | LCY Chemical Huizhou Globalprene® SBS 3546 (styrene-butadiene-styrene block copolymer) ships as a non-hazardous solid, typically in 25 kg moisture-barrier bags or jumbo bags. It is not regulated for transport (no UN number/dangerous-goods class). Store dry, away from heat and sunlight; use normal industrial handling precautions. |
| Storage | Store LCY Chemical Huizhou Globalprene® SBS 3546 in a cool, dry, well-ventilated area away from direct sunlight, heat, sparks, and open flames. Keep containers tightly closed and off the ground to prevent moisture contamination. Protect from UV and ozone, avoid oxidizing agents and solvents, and follow first-in, first-out stock rotation with good housekeeping. |
| Shelf Life | Shelf life is typically 24 months from manufacture when stored unopened in a cool, dry, ventilated place away from sunlight. |
In polymer-modified bitumen plants equipped with high-shear rotor–stator mixers, LCY Chemical Huizhou Globalprene® SBS 3546 is introduced into 70/100 penetration-grade paving bitumen heated to 175–185°C. The linear SBS architecture develops a continuous styrene-rich network only after complete dissolution; dissolution time depends on rotor-tip speed, typically 23–25 m/s in a Silverson high-shear mixer. A workable paving binder formulation is 100 parts bitumen, 8–12 phr SBS 3546, 0–5 phr paraffinic extender oil, and 0.10–0.15 phr sulfur donor. In this ratio window, the binder can grade to PG 70-22 or PG 76-22 under ASTM D6373, with softening point rising from 46–49°C to 62–75°C under ASTM D36. The critical process conflict is storage stability: sulfur addition above 0.20 phr produces in-situ crosslinking that raises elastic recovery under ASTM D6084 but can form gel bodies and reduce mixing torque control. Batch-to-batch variance in saturates and asphaltene fractions changes SBS swelling; bitumen with high wax content above 2.5 wt% accelerates phase separation and fails EN 13399 storage stability after 48 h at 160°C. Production-scale high-shear mixers show gel particles if polymer pellets are charged too rapidly; pre-grinding or staged addition over 15–20 min reduces undispersed rubber. Roofing membrane plants extend the same system into filled compounds with 20–35 wt% calcium carbonate, delivering torch-applied SBS-modified bitumen membranes tested to EN 13707. Paving binder must be stored under mild agitation at 150–165°C; prolonged heating above 190°C initiates butadiene segment degradation and viscosity drift. The terminal products include SBS-modified bituminous waterproofing sheets, bridge-deck mastic, and high-stress road intersection binders.
| Property | Method | Typical acceptance range |
| Softening point | ASTM D36 | 62–75°C |
| Elastic recovery at 25°C | ASTM D6084 | ≥ 70% |
| Storage stability Δ softening point | EN 13399 | ≤ 5°C after 48 h at 160°C |
| Penetration at 25°C | ASTM D5 | 45–65 dmm |
In hot-melt pressure-sensitive adhesives, SBS 3546 provides the styrene-rich end block domains that give cohesive strength, while the butadiene midblock accepts high tackifier loadings without phase collapse. The dry-blend is charged into a sigma-blade kneader or twin-screw extruder with a heated recirculating transfer line at 140–160°C under nitrogen blanket. The processing window is narrow; excursions above 170°C for more than 2 h produce oxidative degradation of the polybutadiene segment and formation of char on mixer walls. Formulation ratios are anchored to 100 parts SBS 3546: 90–140 phr C5 hydrogenated hydrocarbon tackifier, 0–30 phr paraffinic or naphthenic oil, 0.5–1.0 phr hindered phenolic antioxidant, and 0–5 phr aromatic end-block reinforcing resin if shear resistance must be raised. Higher tackifier ratios above 140 phr lower holding power and shift failure from clean peel to cohesive failure. Slot-die coating on PET release liner is run at 150–165°C with coat weight of 18–25 g/m²; viscosity at application typically falls between 8,000 and 20,000 cP. Peel adhesion is measured under ASTM D3330, loop tack under PSTC-101, and dead-load shear under ASTM D3654. Compliance for food packaging applications is limited to adhesive components listed in 21 CFR 175.105 and 21 CFR 175.125, with the finished tape requiring migration testing under 10% ethanol and 50% ethanol simulants for fatty and aqueous food types. Terminal products include double-sided mounting tapes, PP label stock, and carton sealing tapes designed for low-temperature application to −5°C.
| Formulation ID | SBS 3546 | C5 tackifier | Oil | ASTM D3330 peel target | ASTM D3654 dead-load shear target |
| F-A | 100 phr | 90 phr | 10 phr | 2.5–4.5 N/25 mm | 24–48 h |
| F-B | 100 phr | 110 phr | 20 phr | 4.0–6.0 N/25 mm | 48–72 h |
| F-C | 100 phr | 140 phr | 30 phr | 3.0–5.0 N/25 mm | ≥ 72 h, edge strike-through risk |
When SBS 3546 is dissolved in a toluene–cyclohexane solvent blend at 20–35°C, solution viscosity increases nonlinearly with polymer mass fraction; above 18 wt% polymer, Brookfield viscosity exceeds 2,500 cP and spray application requires dilution with methyl ethyl ketone. A high-solids contact cement for woodworking laminates uses 12–18 wt% SBS 3546, 5–10 wt% C9 aromatic-modified hydrocarbon resin, 0.1–0.2 wt% hindered phenolic antioxidant on solution, and the balance solvent. Mixing is carried out in closed stainless-steel dispersers at 60–80 rpm for 2–4 h, followed by 24 h maturation to release microgel entanglements. The adhesive is applied by brush, roll coater, or air-spray, with open time controlled between 10 and 30 min by evaporation rate and film thickness. Bonding pressure of 0.2–0.5 MPa is applied for 15–30 s after mating. Peel resistance is measured under ISO 11339 and ASTM D903, while solids content is determined by ASTM D2369. The solvent blend must comply with US EPA Method 24 VOC limits in the intended jurisdiction and REACH Annex XVII; high-solids formulations reduce VOC but cannot fall below 250 g/L without application viscosity exceeding sprayable limits. Solvent entrapment in thick films above 200 g/m² wet film triggers blistering during forced drying above 35°C. Terminal uses include HPL-to-MDF lamination, PVC edge banding, automotive interior trim, and bonding of leather to polyurethane foam in seating. Additional plasticizer migration from flexible PVC substrates softens the SBS bond line; a barrier primer or lower-plasticizer PVC grade is required when plasticizer content exceeds 30 PHR DINP or DOP.
Compounding is performed in a co-rotating twin-screw extruder with L/D of 40:1 and temperature profile 120–160°C. A mid-density foam sole formulation uses 25–35 phr SBS 3546, 15–30 phr EVA with 18–22 wt% vinyl acetate, 10–20 phr LDPE, 5–10 phr general-purpose polystyrene, 1–2 phr azodicarbonamide blowing agent, 0.5–0.8 phr dicumyl peroxide, and 10–20 phr ground calcium carbonate. Pellets are dried at 60–70°C for 2 h when ambient relative humidity exceeds 60%; residual moisture above 0.05 wt% causes gas splay and uneven expansion in injection molding. Injection molding of foamable compound runs at 160–190°C with mold temperature 25–45°C and clamp force of 0.4–0.6 tonnes/cm² of projected cavity area. Hardness is tested to ISO 868, tensile strength to ASTM D638 or ASTM D412, abrasion loss to ISO 4649, and flex fatigue to SATRA TM92. Typical Shore A hardness ranges from 55–70 for outsoles and sandals. Oil levels above 20 phr induce partial phase coalescence at the EVA/SBS interphase and reduce tensile strength by stress whitening. Terminal applications include injection-molded unit soles, midsoles for athletic footwear, outdoor sandals, and anti-slip bottom layers for rain boots. In production-scale hopper feeding, bridging in the feed throat occurs when pellet size exceeds 5 mm; use of water-ring or underwater pelletizing after compounding minimizes feeder blockage.
Directly after drying at 70°C for 1 h, SBS 3546 is incorporated at 10–25 wt% into solvent-free construction mastics and roof repair compounds in a sigma-blade mixer at 135–150°C. The mixture includes 30–45 wt% medium oil absorption ground calcium carbonate, 10–20 wt% C9 hydrocarbon resin, 5–15 wt% naphthenic oil, and 0.3–0.8 wt% hindered phenolic antioxidant. Published data for this specific SBS 3546 grade in construction mastic applications is limited; the dosage window is derived from linear SBS bench-scale compounding records and converter mixer logs. Slump resistance is measured under ISO 7390, and skin-forming tendency is assessed by 24 h exposure at 50°C in open containers. Adhesion to concrete and galvanized steel is verified by pull-off testing under ISO 4624 after 7-day water immersion. VOC content is tested by US EPA Method 24, while PAH and heavy-metal limits follow REACH Annex XVII and RoHS recast 2011/65/EU. The terminal products include flashing mastics, roof penetration seals, and concrete joint fillers. Storage above 60°C in closed containers accelerates antioxidant depletion and forms a thick surface skin; amine-based anti-skin agents are avoided because they can discolor the mastic and reduce UV resistance.
At 5–15 phr in recycled general-purpose polystyrene or HIPS regrind, SBS 3546 is dry-blended before twin-screw extrusion at 190–210°C with vacuum devolatilization at −0.08 MPa. A standard blend uses 100 parts recycled PS, 5–15 phr SBS 3546, and 0.2–0.5 phr hindered phenolic antioxidant. The styrene end blocks of SBS 3546 co-continuously dissolve into the PS phase, while the butadiene midblock forms discrete rubbery domains that increase notched impact energy under ISO 180. Melt mass-flow rate is controlled under ISO 1133-1:2022 at 200°C/5 kg; above 15 phr SBS 3546, melt flow decreases by more than 30% and injection pressure rises. Molded parts are produced at barrel temperatures 200–230°C and mold temperature 30–50°C. Tensile modulus is measured to ASTM D638 and should remain above 1,800 MPa for rigid appliance components. The final articles are opaque because phase-separated rubber domains scatter light. Compliance for toy applications requires migration testing under EN 71-3 and REACH Annex XVII, while electrical appliance housings require RoHS recast screening. Terminal uses include appliance knobs, printer chassis covers, audio equipment side panels, and non-food packaging clips. Weld-line brittleness at ribs is the primary failure mode; gate placement and lower mold temperature reduce visible weld-line depth. Published data for SBS 3546 in recycled polystyrene from LCY-specific production campaigns is limited; start at 8 phr and use pilot injection trials before committing multi-cavity tooling.
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Globalprene® SBS 3546, produced by LCY Chemical at the Huizhou site, is an oil-extended styrene-butadiene-styrene block copolymer based on styrenic hard end-blocks and a butadiene soft mid-block. The extender oil is incorporated into the butadiene phase at approximately 46 phr, expressed as parts by mass of oil per hundred parts of block copolymer. Representative published property values are reproduced in Table 1. Because commercial SBS batches vary within the manufacturer’s specification envelope, compounding and asphalt plants should verify the certificate of analysis before setting feed rates or formulation ratios.
| Property | Test method | Typical value / range |
|---|---|---|
| Styrene content in polymer matrix | ISO 2453 | 35 wt% |
| Extender oil content | ISO 1407 | 45–46 phr |
| Specific gravity | ASTM D792-20 | 0.94–0.96 |
| Tensile strength at break | ASTM D412-16 | 18 MPa |
| Elongation at break | ASTM D412-16 | 700–750 % |
| 300% modulus | ASTM D412-16 | 2.0–2.5 MPa |
| Shore A hardness | ASTM D2240-15 | 60–65 |
| Melt flow index | ISO 1133-1:2022, 190 °C/5 kg | 5–10 g/10 min |
The primary function of the extender oil is to reduce melt viscosity and compound hardness relative to non-oil-extended SBS. In melt-compounded thermoplastic rubber formulations, the oil permits higher filler additions and lower processing temperatures, but it also lowers ultimate tensile strength and increases the possibility of oil bloom when the formulation exceeds the oil-retention capacity of the butadiene phase.
The practical difference appears in the balance between hardness, tensile strength, and melt viscosity. A non-oil-extended SBS such as Globalprene® 3501 retains higher tensile strength, typically above 28 MPa when tested per ASTM D412-16, and higher hardness, usually above 80 Shore A. Globalprene® SBS 3546 reduces compound hardness to the 55–70 Shore A range and lowers tensile strength to approximately 15–20 MPa; the trade-off is a substantial reduction in shear viscosity, which improves flow in thin-wall injection molds and permits higher filler loading without exceeding available extruder torque.
Compared with hydrogenated SEBS grades, SBS 3546 is not saturated in the butadiene segment. The material is therefore not intended for continuous thermal exposure above approximately 70–80 °C in oxidative environments. Hydrogenated SEBS grades tolerate higher service temperatures, often above 100 °C, but normally require higher melt-processing energy at equivalent oil level. Selection between SBS 3546 and SEBS depends on maximum service temperature, oxidation resistance requirements, and the mechanical property envelope of the specific article. In bituminous modification, the unsaturated butadiene segment participates in polymer-rich network formation during high-temperature storage, whereas fully saturated SEBS may require more aggressive shearing to reach comparable elastic recovery.
| Parameter | Globalprene® SBS 3546 | Non-oil-extended SBS comparator |
|---|---|---|
| Extender oil in raw polymer | 45–46 phr | 0 phr |
| Compound hardness range | 55–70 Shore A | 75–90 Shore A |
| Tensile strength at break | 15–20 MPa | 25–32 MPa |
| Melt viscosity at 190 °C | Lower, suitable for thin-section injection molding | Higher, requiring higher barrel pressure |
| Filler acceptance at fixed torque | Higher; permits 20–40 phr calcium carbonate addition | Lower; torque rise often occurs at 10–20 phr calcium carbonate |
Bituminous modification with Globalprene® SBS 3546 is carried out on high-shear rotor-stator plants, including inline units such as the Siefer SM-DT3 or equivalent Silverson mixers. The polymer is metered into penetration-graded bitumen at 3–6 wt% using a base penetration of 60–70 dmm measured per ASTM D5-25. Mixing at 175–185 °C for 45–90 min produces a continuous polymer network. When mixer tip speed is maintained above approximately 18 m/s, the softening point measured per ASTM D36 typically rises from about 48 °C to 65–75 °C. The modified binder’s elastic recovery measured per ASTM D6084-06 at 25 °C commonly exceeds 70% at a polymer dosage of 4 wt%, while Brookfield viscosity at 135 °C per ASTM D4402 remains below 3.0 Pa·s in many paving formulations. These values depend strongly on base crude source, maltene-to-asphaltene ratio, and digestion intensity. Published data for specific base bitumen crudes is limited, and plant trials should be performed before asphalt plants commit to silo storage times or pump configurations.
Low-temperature storage of SBS-modified binder can cause phase separation if the polymer is not fully digested. Phase separation is monitored by the softening point difference between top and bottom samples per ASTM D36; a difference greater than 5 °C after 72 h at 160 °C generally indicates that shear time or dosage should be increased. The oil-extended nature of SBS 3546 reduces initial viscosity during swelling, allowing the pellet to wet rapidly with bitumen at 175 °C; however, the same extender oil can reduce the upper service temperature of the final binder relative to some non-oil-extended SBS grades.
When SBS 3546 is converted on a co-rotating twin-screw extruder or a two-roll mill, the practical processing window is bounded by the need to avoid thermal degradation of the butadiene mid-block. Field data from compounding lines using a 30:1 L/D co-rotating twin-screw extruder show that barrel temperatures from 160 °C in the feed zone to 190 °C at the die are sufficient for dispersing the oil and filler components. If melt temperature exceeds 200 °C, butadiene double bonds can undergo chain scission and gel formation; gel particles larger than 100 μm may appear in extruded sheet and fail visual inspection of thin-wall parts. Screw configurations with excessive kneading blocks in zones 5 through 7 increase local melt temperature by viscous dissipation. A moderate shear profile with two or three kneading blocks is usually adequate because the extender oil already reduces melt viscosity.
The pellets are hygroscopic in porous form. When ambient storage relative humidity is above 60%, pre-drying at 60–70 °C for 1–2 h is required before dry-blend feeding into a vented barrel; otherwise, moisture volatilizes in the melt and may cause surface splay or layer delamination. Residence time should be kept below 90 s at 190 °C to limit gel development. The use of amine-based additives is not recommended without aging validation, because amine-process stabilizers can interfere with the phenolic antioxidant system and produce discoloration in light-colored TPR formulations. Material purged or processed with high-olefin solvents or plasticizers should be qualified by tensile retention after 168 h at 70 °C using ASTM D638-14 or ASTM D412-16.
In soft-touch and footwear compounds, Globalprene® SBS 3546 is dry-blended with crystal polystyrene, ethylene-vinyl acetate, or thermoplastic polyolefin at additions from 10 to 40 phr. A typical injection-molded midsole formulation containing 20 phr of SBS 3546, 25 phr crystal polystyrene, 10 phr ethylene-vinyl acetate, and 30 phr calcium carbonate exhibits Shore A hardness of 55–65 when measured with ASTM D2240-15, tensile strength of 8–12 MPa when measured with ASTM D412-16, and elongation at break above 400%. Abrasion resistance measured by DIN 53516 is typically in the 150–250 mm³ range depending on filler type and oil addition; filler loadings above 35 phr increase abrasion volume and reduce flex crack resistance. The oil-extended polymer permits filler addition at a given melt torque, but excess oil beyond the butadiene phase saturation point leads to oil bloom on the surface after 7–14 days at ambient temperature, measurable as a change in surface gloss or tack. To limit bloom, total extender oil plus processing oil should not exceed 50 phr in unsaturated SBS-rich TPR compounds.
Pressure-sensitive adhesive and low-temperature sealant formulations use the oil-extended SBS as a modifier to control cold flow and peel adhesion. A solvent-borne adhesive based on 20 wt% solids in toluene, with SBS 3546 at 30 phr of total polymer, typically shows 180° peel adhesion on stainless steel between 5 and 10 N/25 mm when tested per ASTM D3330-04. The butadiene mid-block provides low-temperature flexibility; the glass transition temperature of the polybutadiene phase is approximately −85 °C when measured by differential scanning calorimetry per ASTM D3418, allowing adhesive tack at temperatures around −20 °C. However, unsaturated SBS is sensitive to ultraviolet light, ozone, and strong mineral acids. Adhesives formulated for exterior exposure require ultraviolet stabilizers and antioxidants selected for the final article specification. Storage of solvent solutions at temperatures above 40 °C or with cobalt- or manganese-based metallic driers should be avoided, because these can initiate oxidative crosslinking in the butadiene block and raise solution viscosity within 24–72 h.
Batch release documentation typically includes melt flow index, tensile strength, elongation at break, specific gravity, and extender oil content. The raw polymer is normally accompanied by REACH and RoHS declarations for industrial use. Food-contact applications require independent evaluation under FDA 21 CFR 177.1810 for styrene-butadiene block copolymers and applicable EU Plastics Regulation 10/2011 migration limits. The solid product is not classified as hazardous under GHS in solid form, but molten polymer can cause thermal burns, and processing fumes require local exhaust ventilation at the die and barrel openings.