| HS Code | 857977 |
| Product Name | LCY Chemical Globalprene® SBS 3520 |
| Manufacturer | LCY Chemical |
| Polymer Type | Styrene-butadiene-styrene block copolymer (SBS) |
| Block Structure | Linear |
| Physical Form | Pellets |
| Color | White to off-white |
| Styrene Content | 30 wt% (typical) |
| Butadiene Content | 70 wt% (typical) |
| Density | 0.94 g/cm³ (typical) |
| Melt Flow Rate | 5 g/10 min at 200°C/5 kg (typical) |
| Tensile Strength | 25 MPa (typical) |
| Elongation At Break | 700% (typical) |
| Shore A Hardness | 70 (typical) |
| 300 Percent Modulus | 2.0 MPa (typical) |
| Volatile Matter | ≤0.5 wt% |
| Ash Content | ≤0.2 wt% |
As an accredited LCY Chemical Globalprene® SBS 3520 factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Supplied in 25 kg bags, 40 bags per pallet (1,000 kg net). |
| Container Loading (20′ FCL) | 20′ FCL loading of LCY Chemical Globalprene® SBS 3520 in 25 kg bags, palletized, stretch-wrapped, and secured for ocean shipment. |
| Shipping | LCY Globalprene® SBS 3520 is shipped as a non-hazardous thermoplastic elastomer, typically in 25 kg PE-lined paper bags or 500–1000 kg jumbo bags. Use dry, covered transport and protect from moisture, heat, and ignition sources. No UN number or dangerous-goods class; follow the SDS and local regulations. |
| Storage | Store in a cool, dry, well-ventilated area away from direct sunlight, heat, moisture, and ignition sources. Keep original containers tightly closed and labeled; protect from UV/ozone and prevent dust accumulation. Avoid prolonged storage at elevated temperatures. Maintain good housekeeping, follow local regulations and the SDS, and use oldest stock first. |
| Shelf Life | Typical shelf life is 24 months when stored in a cool, dry, well-ventilated area, protected from direct sunlight and moisture. |
At polymer-modified bitumen plants, addition of Globalprene® SBS 3520 to a 60/70 pen or 70/100 pen base at 3.0–5.5 wt% requires a high-shear rotor-stator mill or in-line colloid mill configured for tip speeds of 18–22 m/s. The 35 wt% bound styrene endblock raises upper service temperature once a continuous polymer network forms, but it also narrows the mixing window before phase inversion. Milling time of 60–120 min at 170–190 °C is typically required to reduce the SBS phase to a particle diameter below 10 µm; incomplete dispersion leaves large polymer domains that fail to deliver elastic recovery and produce unstable hot storage. A Siefer Trigonal or equivalent in-line colloid mill with rotor-stator geometry is preferred over low-shear paddle blending. After dispersion, the concentrate is transferred to a maturation tank with low-shear agitation at 160–175 °C for 60–180 min; temperatures above 200 °C degrade the butadiene midblock and are observed as viscosity rise, gel specks, and blocked filter elements.
Sulfur crosslinking at 0.05–0.15 wt% ground sulfur or an equivalent sulfur donor stabilizes the polymer network and reduces the softening point difference measured under EN 13399. Sulfur addition above 0.2 wt% accelerates gelation, blocks transfer pumps, and creates non-conforming elastic response. Binder selection interacts with maltene/asphaltene ratio; aromatics-poor feedstocks may require 1–3 phr aromatic extender oil to improve polymer solvency. Brookfield viscosity at 135 °C per ASTM D4402 is commonly 1.5–3.5 Pa·s; values above 4.0 Pa·s require higher preheat and can starve the mill inlet. Quality-control limits for a 4.5 wt% SBS 3520 formulation in 70/100 pen base normally fall within softening point 65–75 °C per ASTM D36, elastic recovery at 25 °C of 80–95% per ASTM D6084-21, and MSCR Jnr at 3.2 kPa below 0.5 kPa−1 per AASHTO T350.
| Property | Standard method | Typical PMB control target |
|---|---|---|
| Softening point (R&B) | ASTM D36 / EN 1427 | 65–75 °C |
| Penetration at 25 °C | ASTM D5 / EN 1426 | 45–60 dmm |
| Elastic recovery at 25 °C | ASTM D6084-21 / EN 13398 | ≥80% |
| Storage stability Δ softening point | EN 13399 | ≤5 °C |
| MSCR Jnr at 3.2 kPa | AASHTO T350 | ≤0.5 kPa−1 |
Continuous hot-melt compounding of Globalprene® SBS 3520 in tackified pressure-sensitive adhesive systems is constrained by the 35 wt% styrene endblock content and the shear sensitivity of the polybutadiene midblock. The grade is processed in a co-rotating twin-screw extruder with an L/D ratio of 36–48 and barrel zone settings from 120 °C at the feed throat to 165–175 °C at the slot die. C5 aliphatic tackifying resins with a ring-and-ball softening point of 90–110 °C are used at tackifier/SBS ratios of 1.0:1–3.0:1; naphthenic process oil at 0.2:1–1.0:1 reduces melt viscosity, but oil loadings above 1.0:1 cause tackifier migration, die-lip buildup, and loss of peeling energy. Brookfield viscosity per ASTM D3236 at 180 °C for a 40 wt% polymer/tackifier system is typically in the 2,000–8,000 mPa·s range; formulations outside this range may require gear-pump pressure above 100 bar or exhibit coating-weight variation.
Peel adhesion at 180° per ASTM D3330/D3330M on stainless steel for a 50 µm coat weight is commonly specified between 8–20 N/25 mm, while loop tack per ASTM D6195 and static shear holding power per ASTM D3654 define the service envelope. On packaging lines, a 200 µm slot-die gap and line speeds of 50–150 m/min are typical; melt temperatures above 185 °C generate char particles that deposit on the die lips and create adhesive film defects. The unsaturated butadiene block makes hot-melt aging at 180 °C for more than 8 h a practical boundary before colour shift and viscosity drift become measurable. For indirect food-contact tape and label uses, the formulated adhesive must comply with FDA 21 CFR 175.125; system suppliers should provide batch-specific declarations of compliance for tackifiers and process oils.
High dilution with toluene in solvent-borne assembly adhesives lowers application viscosity but destabilizes the endblock network of Globalprene® SBS 3520. In a toluene/n-hexane/MEK mixture at 25–40 wt% solids, the 35 wt% styrene endblock content produces higher solution viscosity than lower-styrene SBS grades at equal solids. Dilution below 20 wt% solids is often required for roller coatability, which decreases applied dry film thickness and increases solvent recovery load. A jacketed dissolver with an anchor speed of 40–60 rpm and a high-speed disperser tip speed of 7–12 m/s is used; SBS pellets must be added slowly under anchor rotation to avoid fisheye formation. Adding aliphatic hydrocarbon solvent to reduce viscosity raises cloud point and shifts the endblock solvation boundary, so polar MEK or ethyl acetate is held at 5–15 wt% of the solvent blend to restore phase stability during flash-off.
Production-scale solvent mixing is carried out under nitrogen inerting because toluene/n-hexane vapours fall under ATEX 1999/92/EC zoning and require explosion relief. Peel adhesion per ASTM D3330/D3330M and T-peel per ASTM D1876 on solvent-cast films are used for batch release; lap shear strength per ASTM D1002 defines the structural boundary. Solvent recovery under vacuum at 200–250 mbar and jacket temperature 60–80 °C avoids foamover; residual solvent is monitored by gas chromatography. Aromatics content is the principal regulatory limit; many low-VOC factory permits restrict toluene and keep total VOC below 250 g/L. Published data for Globalprene® SBS 3520 in high-toluene dilution is limited; coating trials should characterize viscosity stability at 24 h and 48 h after letdown because delayed solution gelation can appear as surging at the coater.
In injection-moulded footwear sidewall and single-unit outsole compounds, Globalprene® SBS 3520 is conventionally blended with crystal polystyrene, paraffinic oil, calcium carbonate, and antioxidant packages in a Banbury internal mixer or co-rotating twin-screw extruder. Crystal polystyrene at 20–40 phr raises hardness and abrasion resistance but narrows the processing window; paraffinic oil at 10–50 phr controls flow and permits hardness adjustment between 55 Shore A and 75 Shore A per ASTM D2240. Calcium carbonate filler at 15–35 phr lowers compound cost but reduces tear strength and increases density. A Banbury drop temperature of 165–180 °C followed by a two-roll mill at 90–110 °C produces a strip-fed pellet; melt temperatures above 195 °C cause butadiene segment degradation and brown discolouration, while temperatures below 170 °C leave undispersed polystyrene and create hard spots. Pellets should be pre-dried at 70–80 °C for 2–4 h if storage humidity exceeds 60% RH to prevent surface splay.
Injection moulding uses a screw L/D of 20–24 and compression ratio of 2.5:1–3.0:1, with a barrel profile of 170–195 °C, injection pressure 70–100 MPa, and mould temperature 30–60 °C. Short shots and jetting appear below 60 MPa injection pressure or below 170 °C melt temperature; burning and surface splay appear above 200 °C. Abrasion loss per DIN 53516 is typically 250–400 mm³ for a 65 Shore A compound, trouser tear per ISO 34-1 is typically 25–45 kN/m, and compression set per ASTM D395 at 23 °C/70 h is 25–40%. High moulded-part gloss requires mould temperatures above 45 °C, but cycle-time extensions become measurable. Production lines often run multicavity moulds with hot or cold gate systems; unbalanced runner layouts create density and hardness variation across cavities.
Impact modification of injection-grade polypropylene homopolymer with Globalprene® SBS 3520 is performed on a co-rotating twin-screw extruder with an L/D ratio of 40–52 and a side feeder for the elastomer. Barrel temperatures are set from 190 °C at the feed throat to 205–225 °C at the die. SBS addition at 5–15 wt% raises notched Izod impact strength per ASTM D256-23 at 23 °C from the unmodified PP baseline of 2–3 kJ/m² to 10–25 kJ/m² depending on particle-size distribution and screw shear. Low-temperature impact at −20 °C improves to a lesser extent because the polybutadiene midblock stiffens below its glass transition; published data for Globalprene® SBS 3520 in PP is limited compared with SEBS and requires internal design-of-experiment validation. Tensile yield stress per ASTM D638-14 declines as SBS content rises, typically by 15–25% at 15 wt% addition. Melt flow rate per ISO 1133-1:2022 at 230 °C/2.16 kg drops from 25 g/10 min for unmodified PP to 8–15 g/10 min at 15 wt% SBS.
A phenolic/phosphite antioxidant pair at 0.2–0.4 phr is mandatory above 210 °C barrel temperature to suppress chain scission in the unsaturated midblock; without stabilizer, discolouration and a secondary MFR rise are observed after 15 min residence time. Dispersion quality depends on side-stuffer feed rate and screw speed; an excessively high feed rate floods the melting zone and produces large elastomer domains visible in ASTM D256 fracture surfaces. Injection moulding of PP/SBS compounds uses a clamp force of 1.5–3.0 kN/cm² of projected area and a mould temperature of 20–60 °C. The blend is not suitable for hot-water contact at 80 °C for extended service due to oxidative attack of the polybutadiene block; formulations requiring such exposure should use SEBS or EPDM-modified PP.
Torch-applied SBS-modified bituminous waterproofing membranes require a compound that retains low-temperature flexibility after mineral filler loading and withstands torch heating without excessive flow. Globalprene® SBS 3520 is compounded into a distilled or oxidized bitumen at 8–14 wt% for the membrane coating compound, with ground limestone filler at 20–40 phr and sometimes a petroleum resin to adjust tack. High-shear mixing at 180–190 °C is followed by spreading at 150–170 °C onto a polyester or glass-fibre reinforcement. Low-temperature flexibility is tested per ASTM D5147/D5147M on a 25 mm mandrel at −10 to −20 °C without cracking; softening point per ASTM D36 is typically specified above 95 °C, and penetration at 60 °C per ASTM D5 is held below 20 dmm to resist sliding on sloped roofs. Filler loading above 30 wt% raises compound viscosity to levels that exceed positive displacement pump capacity on high-speed spreader lines, producing surging and coating weight variation.
Production-scale membrane lines show surface blistering when mixing or spreading temperatures exceed 200 °C because volatile degradation products from the butadiene block nucleate bubbles in the coating compound. Torch installation exposes the underside to flame; proper torching technique is a site safety limit rather than a material property, but the compound must remain embossed and dimensionally stable during localized heating. Dimensional stability per EN 1107-1 is controlled by filler and reinforcement; watertightness is tested under the full assembly per EN 1928. Batch records should track melt viscosity at 180 °C per ASTM D4402 because viscosity drift indicates storage-time degradation in transfer tanks held at 160–175 °C.
| Membrane property | Standard method | Control range |
|---|---|---|
| Low-temperature flexibility on 25 mm mandrel | ASTM D5147/D5147M | −10 °C no cracks |
| Softening point (R&B) | ASTM D36 | ≥95 °C |
| Penetration at 60 °C | ASTM D5 | ≤20 dmm |
| Dimensional stability | EN 1107-1 | ≤0.5% |
| Watertightness | EN 1928 | No water penetration per assembly test program |
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LCY Chemical Globalprene® SBS 3520 is a linear styrene-butadiene-styrene triblock copolymer supplied as a porous pellet or crumb. The grade designation is generally interpreted as containing a nominal bound styrene mass fraction of 35 wt% and an oil-extension level of 20 phr, although lot-specific certificates of analysis must govern compounding calculations. The polystyrene end-blocks form glassy associative domains with a glass transition near 95 °C, while the polybutadiene mid-block forms a rubbery continuous phase with a glass transition near −80 °C. Because the mid-block contains unsaturation, the material can be melt reprocessed through the polystyrene domain melting transition, but it is sensitive to oxidative degradation at elevated temperatures and under ozone or ultraviolet exposure. Published data for this specific grade configuration is limited in public repositories, so process windows should be verified against the manufacturer’s technical data sheet for the received lot.
The linear architecture is produced by sequential anionic polymerization. A low diblock fraction is preferred because residual styrene-butadiene diblock chains behave as network defects under strain and reduce tensile strength at break in ISO 37 tensile specimens. Quality-control documentation for styrenic block copolymers typically reports bound styrene content by ASTM D5775, oil content by ASTM D297 extraction, melt-flow rate by ISO 1133-1:2022 at 200 °C under 5 kg, and Shore A hardness by ISO 868. Downstream compounders commonly use these values to set extruder throughput and to maintain batch-to-batch consistency.
Selection of Globalprene® SBS 3520 for a given process is governed by bound styrene content, oil content, diblock content, solution viscosity, melt-flow rate, tensile set, and gel mass. Bound styrene content serves as a first-order predictor of hardness and tensile strength; oil content controls melt rheology and low-temperature properties; diblock content influences ultimate tensile strength and tensile set; melt-flow rate indexes processability in injection moulding and asphalt equipment. The grade designation therefore allows compounders to compare the oiled grade with low-oil SBS grades without first running a full compositional analysis.
Laboratory methods include ASTM D5775 for bound styrene, ASTM D297 for extractables, ISO 1183 for density, ISO 868 for Shore A hardness, ISO 37 for tensile stress-strain properties, ISO 815-1 for compression set, and ISO 1133-1:2022 for melt-flow rate. Gel mass is determined by dissolving the polymer in toluene, filtering through a 200 mesh screen, and drying the residue; specifications for oil-extended SBS grades commonly set gel mass below 0.1% to avoid surface defects in thin films and adhesives.
| Attribute | Globalprene® SBS 3520 | Oil-free linear SBS | SEBS | SBR |
|---|---|---|---|---|
| Mid-block unsaturation | High; oxidizable | High; oxidizable | Low; hydrogenated | High; oxidizable |
| Thermoplastic reprocessability | Yes | Yes | Yes | No; vulcanization required |
| Typical melt processing window | 170–200 °C | 180–210 °C | 220–250 °C | 140–170 °C |
| Ozone and ultraviolet resistance | Moderate to poor | Moderate to poor | High | Moderate to poor |
| Bitumen solubility | High after swelling | High after swelling | Moderate; slower swelling | Moderate |
| Compression set after 24 h at 70 °C | Higher than SEBS | Higher than SEBS | Low | Vulcanization-dependent |
Regulatory status for REACH, RoHS, and United States FDA 21 CFR depends on the specific formulation and lot. The supplier compliance certificate should be consulted before use in food-contact or medical applications.
In polymer-modified bituminous binder production, Globalprene® SBS 3520 is usually added at 3 wt% to 7 wt% based on bitumen mass. The polymer is wetted by maltenes and must be dispersed under high shear. A rotor-stator mill operating at tip speeds of 15 m/s to 25 m/s and a bulk temperature of 175 °C to 190 °C is standard; mixing times of 60 min to 120 min are common, but low-aromaticity binders may require longer swelling. Below the critical polymer concentration, usually 4 wt% to 6 wt% for many 50/70 and 70/100 penetration-grade binders, the polymer exists as a dispersed phase and does not develop a continuous elastic network. Above that concentration, the polystyrene domains act as physical junctions and the bitumen phase becomes polymer-rich, raising softening point and elastic recovery.
The high-shear processing window is narrow. Temperatures above 200 °C increase bitumen viscosity and accelerate free-radical oxidation of the unsaturated polybutadiene mid-block; the resulting gel particles can blind downstream filters and produce surface defects in the final pavement or waterproofing membrane. Conversely, temperatures below 170 °C may not reduce bitumen viscosity sufficiently for effective shear transfer. The practical window on some production lines is therefore 170–190 °C, with excursions above 200 °C limited to less than 30 min. Published data for LCY SBS 3520 in specific crude-sourced bitumens is limited, so the critical addition level and mixing time should be established by laboratory blending on the actual binder.
Routine acceptance tests after mixing include ASTM D36 ring-and-ball softening point, ASTM D6084 elastic recovery at 25 °C, ASTM D4402 Brookfield rotational viscosity at 135 °C, and AASHTO M320 performance-grade determination after rolling thin-film oven aging and pressure-aging vessel aging. Storage stability is evaluated by EN 13399 separation testing; an acceptable system often shows a softening-point difference of less than 2.5 °C after 48 h at 163 °C. If separation exceeds this limit, aromatic-rich extender oil or reactive stabilization is commonly adjusted.
On production units, the polymer is often fed through a screw feeder into a recirculating bitumen stream; inadequate swelling is observed as a grainy dispersion when a thin film is drawn. Dispersion quality is assessed by fluorescence microscopy, where a continuous polymer-rich phase indicates good dispersion and polymer-poor regions indicate underdosing or insufficient shear. Circulation pump cavitation can occur when binder viscosity exceeds 3.5 Pa·s at 135 °C; trace heating and positive-displacement pumps are used on lines handling SBS-modified binders.
Compounding of Globalprene® SBS 3520 on a 43:1 L/D co-rotating twin-screw extruder generally uses barrel set points from 140 °C at the feed throat to 185 °C at the die. Because the grade is oil-extended, free oil injection should be reduced by the nominal 20 phr already present. When additional naphthenic oil is required, it is injected after the polymer is fully melted at barrel 5 to barrel 7 to prevent screw slip and torque instability. A screw speed of 250 rpm to 350 rpm is typical, but residence time above 200 °C should not exceed 2 min; longer thermal exposure increases gel mass and can produce black specks in extrudate. Batch-to-batch variation in solution viscosity can shift screw torque by approximately 10–15%, so feed-rate trim should be used to keep motor load below 85% of nameplate.
For injection moulded footwear soles, the material is typically processed with barrel profiles of 160–190 °C and injection pressures of 80–120 MPa. Mould temperatures are kept low, usually 10–30 °C, to freeze the polystyrene domains rapidly and reduce cycle time. Clamp force calculations commonly use 0.5–0.8 kN/cm² of projected cavity area. If the pellets have been stored at relative humidity above 70%, hot-air drying at 70 °C for 2 h is applied; moisture above 0.1% has been observed on production machines as splay and surface roughness in soles.
The unsaturated polybutadiene mid-block is the primary stability constraint. Allylic hydrogens in the 1,4-polybutadiene repeat units are susceptible to abstraction, forming hydroperoxides that decompose into alkoxy and peroxy radicals. Once radical propagation begins, molecular weight can increase through crosslinking and decrease through chain scission simultaneously; gel formation and discoloration are observed before major loss of melt flow. Published kinetic work on 1,4-polybutadiene places the onset of rapid autoxidation above 150 °C in air, and the rate rises sharply as the melt approaches 200 °C. Hot-melt processes are therefore usually run under a nitrogen blanket or with antioxidant packages containing hindered phenols and phosphites. Amine-based antioxidants are generally limited in light-coloured goods because they can cause color drift; copper and cobalt soaps should be excluded because they catalyze unsaturated mid-block oxidation.
Comparative oxidation induction time can be measured by differential scanning calorimetry under ASTM D3895-19, although this method was developed for polyolefins and should be used as a relative ranking tool rather than an absolute predictor of service life. Prolonged outdoor exposure is typically evaluated by ASTM G154 fluorescent UV weathering; SBS 3520 will exhibit surface cracking and gloss loss unless formulated with carbon black, UV stabilizers, or a protective coating. The continuous service upper limit is approximately 80 °C under load because polystyrene domain softening reduces modulus; peak temperature excursions should not exceed 100 °C for non-load-bearing parts.
Formulation-level stabilization commonly combines a hindered phenolic primary antioxidant at 0.05–0.15 phr with a phosphite secondary antioxidant at 0.05–0.10 phr. Carbon black at 2–5 phr is used for ultraviolet shielding in outdoor compounds. These are compounding guidelines, not product specifications; the melt stability of the received lot should be checked by a torque-rheometer test at 180 °C for 30 min.
Relative to an oil-free linear SBS of comparable bound styrene content, Globalprene® SBS 3520 has lower melt viscosity and lower Shore A hardness because the incorporated oil plasticizes the rubbery phase. The trade-off is reduced tensile strength and modulus in ISO 37 tests; oil-free grades are preferred for high-hardness injection moulded goods, while the 3520 grade is more often selected for bituminous modification, soft compounds, sealants, and adhesives where lower viscosity and wetting are required. The oil extension also reduces internal polymer friction and can permit direct addition to asphalt without a separate oil pre-blend.
Compared with SEBS, SBS 3520 processes at lower barrel temperatures and dissolves more readily in toluene and hot bitumen, but its unsaturated mid-block gives inferior ozone resistance, long-term heat aging, and retention of elongation after weathering. SEBS grades are often specified when the part must withstand continuous temperatures above 100 °C or repeated steam sterilization; SBS 3520 is not recommended for those conditions. Compared with SBR, the thermoplastic network of SBS 3520 permits melt reprocessing without sulfur vulcanization, but vulcanized SBR has better hot tensile strength, lower compression set at elevated temperatures, and better resistance to hydrocarbon solvents once crosslinked. SBS 3520 also differs from SIS and mixed diene adhesive grades because the polystyrene content provides higher cohesive strength but lower room-temperature tack.
In bitumen, the solubility difference between SBS and SEBS is critical. SBS swells rapidly in maltenes at 180 °C, whereas SEBS often requires higher shear and longer residence. The unsaturated SBS also thermally crosslinks at high temperature, which can be beneficial in roofing formulations when controlled, but creates storage stability risks in paving binders. Within the broader styrenic block copolymer range, higher bound styrene content raises softening point and hardness but reduces low-temperature flexibility; the oil extension in the 3520 grade offsets part of that hardness increase.
Hot-melt pressure-sensitive adhesive formulations using SBS 3520 typically incorporate tackifier resins with softening points in the 85–115 °C range and remain processable in slot-die coaters at 160–180 °C. The oil-extended viscosity reduces coating pressure, but the formulation must be protected from oxygen at the application head; viscosity drift of more than 10% during an 8 h production shift indicates gel formation and requires an inert atmosphere or antioxidant adjustment. In polypropylene impact modification, the grade is added at 5–15 wt% using a twin-screw extruder; above 15 wt% the dispersed SBS phase can coarsen and reduce weld-line strength in injection mouldings, a behavior assessed by ISO 527-2 tensile testing of double-gated specimens.