| HS Code | 171091 |
| Polymer Type | styrene-butadiene-styrene block copolymer |
| Structure | linear triblock |
| Styrene Content | 31% |
| Butadiene Content | 69% |
| Diblock Content | 16% |
| Oil Content | 0 phr |
| Density | 0.94 g/cm³ |
| Melt Flow Rate | 3.0 g/10 min at 200°C/5 kg |
| Shore A Hardness | 75 |
| Tensile Strength | 24 MPa |
| Elongation At Break | 700% |
| 300 Modulus | 2.3 MPa |
| Volatile Matter | ≤0.5% |
| Ash Content | ≤0.2% |
| Appearance | white pellets |
As an accredited LCY Chemical Globalprene® SBS 3741 factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | LCY Globalprene® SBS 3741 is supplied in 25 kg moisture-resistant bags, palletized for industrial storage and handling. |
| Container Loading (20′ FCL) | LCY Globalprene® SBS 3741 is loaded in 25 kg bags into a 20′ FCL, palletized, shrink-wrapped, and secured for transport. |
| Shipping | LCY Chemical Globalprene® SBS 3741 is shipped as a non-hazardous thermoplastic elastomer in moisture-proof 25 kg bags or jumbo bags on pallets. It is not classified as dangerous goods; keep dry, cool, ventilated, and away from ignition sources and direct sunlight during transport. |
| Storage | Store LCY Chemical Globalprene® SBS 3741 in a cool, dry, well-ventilated warehouse away from direct sunlight, heat, ignition sources, and moisture. Keep original containers tightly closed and palletized; avoid prolonged UV/ozone exposure. Maintain moderate temperature and humidity, separate from strong oxidizers, acids, and solvents, and follow SDS/local regulations with first-in, first-out stock rotation. |
| Shelf Life | Typical shelf life is 24 months when stored unopened in original packaging in a cool, dry, ventilated area away from direct sunlight. |
In direct-injection footwear lines, Globalprene® SBS 3741 is processed as the base elastomer for expanded microcellular soles. The polymer is pre-blended with paraffinic process oil at 8 to 15 phr, precipitated silica at 5 to 10 phr, azodicarbonamide blowing agent at 1.2 to 2.0 phr, zinc oxide at 0.8 to 1.2 phr, and stearic acid at 0.5 to 1.0 phr. Compounding is conducted in a co-rotating twin-screw extruder with L/D ratio 36 to 44, using barrel temperatures from 120 °C to 150 °C and a screw speed of 250 to 400 rpm. Pelletized compound is dried to 0.02 % moisture before direct injection on rotary multi-station machines with clamp force between 35 tonnes and 80 tonnes. Injection cylinder temperatures are maintained at 150 °C to 170 °C, mold temperature is held at 30 °C to 50 °C, and injection pressure is controlled between 50 MPa and 70 MPa. Apparent density is specified between 0.25 g/cm³ and 0.45 g/cm³ according to ISO 845. Shore A hardness is monitored under ISO 868. Finished articles include running shoe midsoles, casual sandal soles, and expansion-molded comfort footwear. Compliance screening applies REACH Annex XVII entry 50 limits for the eight listed polycyclic aromatic hydrocarbons in rubber components with direct skin contact. Reclaim of granulated sole scrap containing residual azodicarbonamide is restricted to 5 wt% or less because higher addition levels shift cell size distribution and cause density scatter. Lot-to-lot variance in oil absorption should be checked against the supplier certificate of analysis before scale-up because porosity defects arise at the injection gate when compound viscosity drops more than 10 % from baseline.
In hot-melt pressure-sensitive adhesive compounding, Globalprene® SBS 3741 is charged as the styrenic block elastomer at 100 phr with a tackifying resin system at 100 to 130 phr and naphthenic process oil at 20 to 40 phr. Hydrogenated rosin ester or C5/C9 aliphatic-aromatic resin is selected based on the storage temperature of the finished label or tape. A hindered phenolic antioxidant is added at 0.3 to 0.5 phr and a phosphite co-stabilizer at 0.2 phr to suppress gel formation in the unsaturated polybutadiene midblock. Mixing is executed in a jacketed sigma-blade kneader at 160 °C to 175 °C for 45 to 90 min under nitrogen blanket. Apparent viscosity after mixing is measured at 165 °C with a Brookfield Thermosel under ASTM D3236-14. Slot-die coating is performed at 150 °C to 165 °C with coat weights between 15 g/m² and 25 g/m². Loop tack is measured under FINAT FTM 9; 180° peel adhesion is measured under PSTC-101 Test Method A. Static shear adhesion after 7 days at 70 °C is screened under ASTM D3654-12; shear adhesion failure temperature is evaluated by ASTM D4498-07(2015). Adhesive systems for food packaging side seams are screened under FDA 21 CFR 175.105 and repeated-use rubber articles under FDA 21 CFR 177.2600. Melt hold time must not exceed 3 h at 175 °C to avoid chain scission and darkening. Finished goods include carton sealing tapes, label stock, and film-backed mounting tapes. Outdoor exposure without UV-blocking face stock reduces peel retention due to oxidation of the diene midblock.
The binder recipe is based on a penetration-grade bitumen such as 70/100 or 50/70 with Globalprene® SBS 3741 added at 3.0 to 5.5 wt% of the final binder mass. An optional sulfur crosslinking agent at 0.05 to 0.15 wt% is metered after the polymer swelling stage to stabilize the SBS network without producing excessive gelation. High-shear dispersion is conducted in a rotor-stator mill at 3,500 rpm to 5,000 rpm and 180 °C to 190 °C for 60 to 120 min. The mill is stopped when the torque plateau after polymer addition is stable for 15 min. The finished PMB is stored in nitrogen-blanketed horizontal tanks with low-agitation paddles at 160 °C to 170 °C. Release tests include softening point by ASTM D36-14, penetration by ASTM D5-19, elastic recovery by ASTM D6084-18, and storage stability by EN 14023:2010 using the 72-h tube test procedure. A storage-stable PMB for dense-graded road surfacing normally maintains a softening point difference below 2.5 °C after 72 h. Terminal products include heavy-duty pavement binders, airport runway mastics, and high-stress intersection wearing courses. The styrenic domains of 3741 provide network strength, while the diene midblock absorbs maltenes and imparts elastic recovery. Filler addition before complete dispersion is held below 5 wt% of total binder unless performance-grade verification is carried out under AASHTO M320-21. Published data for this specific configuration is limited, so mixer torque logs and softening point pull samples are used as primary scale-up records.
Solvent-borne contact adhesives for furniture lamination and automotive headliner layup use Globalprene® SBS 3741 as a partial replacement for chloroprene rubber. A high-solids sprayable system contains 100 phr of total elastomer, of which 20 to 40 phr is 3741 and the balance is modified chloroprene. Tackifying resin is charged at 40 to 60 phr, magnesium oxide at 4 phr, zinc oxide at 2 phr, and hindered phenolic antioxidant at 1 phr. The solvent blend comprises acetone, cyclohexane, and methyl ethyl ketone at a total solids content of 12 to 18 wt%. Mixing proceeds in a closed vacuum dissolver at 1,000 rpm until the final viscosity is 300 to 600 mPa·s at 25 °C. The adhesive is applied by HVLP spray or roller coater at 150 g/m² to 200 g/m² wet film. Drying time before lamination is 30 to 60 min at 25 °C. Peel strength is determined by ASTM D903-98(2017) or ISO 11339:2018. Solvent management obligations for coating and adhesive installations are assessed under Directive 2010/75/EU. Hydrophobic fumed silica is added at 0.5 to 1.5 phr to reduce sag on overhead surfaces. Finished products include laminated kitchen worktops, automotive door panel composites, and acoustic foam-backed headliners. Because the butadiene midblock is unsaturated, these contact adhesives are not specified for prolonged UV exposure without a protective coating or opaque coverstock.
In modified bituminous membrane production, Globalprene® SBS 3741 is incorporated into oxidized or distillation-grade bitumen at 8 to 12 wt% of the coating compound. Limestone powder filler is added at 25 to 35 wt%, and a styrenic-compatible sulfur donor is used at 0.1 to 0.2 wt% where high-temperature flow resistance is required. A horizontal plough mixer or vertical high-shear bitumen plant is heated to 170 °C to 190 °C. Dispersion is complete when the mixer torque stabilizes after the polymer swelling phase, usually 90 to 150 min from the final polymer addition. The coating compound is applied on a polyester or glass-fibre carrier through calender rolls controlling thickness between 3 mm and 6 mm. Cold flexibility is tested under EN 1109:2014; heat resistance and flow resistance are assessed under EN 1110:2010. Final sheets are sold as torch-applied waterproofing membranes for concrete bridge decks, basements, and roofs. Conformity is declared under EN 13707:2013 for flexible sheets for waterproofing; North American projects may reference ASTM D6164-19 for SBS-modified bitumen sheet materials. The addition level is lowered to 6 wt% only when the substrate is fully embedded and no torch reheating is specified in the project specification. Lower polymer content reduces low-temperature flexibility below -10 °C as measured by EN 1109:2014.
For injection-molded soft-touch automotive and appliance parts, Globalprene® SBS 3741 is let down with polypropylene homopolymer in a co-continuous thermoplastic elastomer compound. A practical starting ratio is 100 phr 3741, 30 to 50 phr polypropylene homopolymer with melt flow rate 20 to 40 g/10 min at 230 °C/2.16 kg, 20 to 40 phr paraffinic oil, and 0.1 to 0.3 phr processing stabilizer. Compounding is performed in a co-rotating twin-screw extruder with L/D ratio 32 to 40, using starve feeding and downstream oil injection after the first 8 barrel segments. Barrel temperatures ramp from 150 °C at the feed throat to 190 °C at the die. Pelletized TPE is dried at 60 °C for 2 h when storage relative humidity exceeds 60 %. Injection molding uses clamp force from 500 kN to 1,800 kN, injection pressure between 60 MPa and 90 MPa, and mold temperatures of 20 °C to 45 °C. Hardness is controlled between Shore A 45 and 65 under ISO 868. Tensile properties are measured according to ISO 37:2017. Melt flow rate is measured by ISO 1133-1:2022. Electrical and electronic compliance is documented under IEC 62321-5:2013 for lead and cadmium and IEC 62321-8:2017 for phthalates. Finished articles include appliance feet, cable grommets, gear lever bellows, and floor mat edge strips. Prolonged outdoor exposure is limited because the unsaturated butadiene segment is susceptible to oxidation unless UV-stabilized masterbatches are added at 1.0 to 2.0 wt%.
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LCY Chemical Globalprene® SBS 3741 is a styrene-butadiene-styrene block copolymer supplied as a porous pellet. The grade is assembled from polystyrene terminal blocks and a polybutadiene midblock, giving a physically crosslinked network at service temperature while retaining melt processability. Within the Globalprene SBS range, SBS 3741 is positioned as a low-styrene, oil-extended material with a bound styrene content of 31 wt% and a nominal oil extension level of 37.5 phr. The extension oil reduces melt viscosity and lowers Shore A hardness relative to unextended SBS types, but it also reduces the cohesive strength available from the styrene domains. The grade is therefore selected when low-temperature flexibility, substrate wetting, or high-shear dispersion in bitumen is more important than elevated-temperature stiffness.
The typical property profile is reproduced below from LCY technical literature as a release-range summary rather than a batch specification. Lot-to-lot variation is controlled primarily through melt mass-flow rate, oil content, and tensile response.
| Property | Test method | Typical range |
|---|---|---|
| Melt mass-flow rate at 190 °C / 5 kg | ISO 1133-1:2022 | 1.5–3.0 g/10 min |
| Bound styrene content | Internal extraction/IR | 30–32 wt% |
| Oil extension level | Internal extraction | 37.5 phr |
| Hardness | ASTM D2240-15 | 50–65 Shore A |
| Tensile strength at break | ASTM D638-14 | 15–22 MPa |
| Elongation at break | ASTM D638-14 | 700–800% |
| Specific gravity | ISO 1183-1 | 0.93–0.95 |
| Volatile matter | Gravimetric | <0.5 wt% |
The melt mass-flow rate is an inverse processing parameter rather than a direct molecular-weight specification. Because the grade is oil-extended, MFR alone does not distinguish between a high-molecular-weight backbone with high oil let-down and a lower-molecular-weight backbone with lower oil let-down. Quality-control laboratories therefore cross-check MFR against tensile strength and Shore A hardness after compression molding, using conditioning at 23 °C and 50% RH for 24 h. A simultaneous loss of tensile strength and hardness at constant MFR typically indicates a shift in butadiene block length or oil distribution, not merely a viscosity change.
Higher-styrene grades such as Globalprene SBS 3540 and SBS 3545 carry bound styrene levels of 40–45 wt%. The additional polystyrene terminal blocks increase the volume fraction of hard domains, which raises Shore A hardness, tensile strength, and the temperature at which the network begins to creep. Those grades are selected for compounds that must survive deformation at 70 °C or that require resistance to polar solvents. SBS 3741, at 31 wt% bound styrene and 37.5 phr extension oil, accepts a lower tensile ceiling because the hard-domain volume fraction is smaller and the oil further separates the styrene domains. The resulting material develops lower melt viscosity, better low-temperature flexibility, and faster wetting on porous or low-energy substrates. The trade-off is a reduced upper service temperature and lower cohesive strength in adhesive bonds.
Compared with unextended SBS 3501, which is also a low-styrene triblock, SBS 3741 can be processed at lower melt temperature and disperses more readily in asphalt and in low-shear mixers. The pre-dispersed extension oil also shortens the time needed to reach equilibrium compound hardness. However, the formulator loses the ability to independently select the oil type and level because the extension oil is already part of the commercial pellet. Compared with SIS block copolymers, SBS 3741 offers higher room-temperature cohesive strength but lower initial tack. Compared with SEBS, SBS 3741 retains unsaturation in the butadiene midblock and therefore requires stabilization against ultraviolet and thermo-oxidative degradation.
In solvent-based contact adhesives, a 20 wt% solids solution of SBS 3741 in a toluene/hexane blend develops lower Brookfield viscosity than an equivalent solids solution of unextended SBS 3540. This permits a reduction in solvent demand during roll-coating or a higher coating speed before ribbing defects appear. Aliphatic C5 tackifying resins are preferred over aromatic C9 resins when low-temperature flexibility must be preserved because aromatic resins stiffen the styrene domains. The relevant peel test is ASTM D903-17, though published data for this specific SBS 3741 formulation configuration is limited.
In asphalt modification, production-scale incorporation uses a rotor-stator high-shear mill with the bitumen preheated to 150 °C before polymer addition. The SBS 3741 pellets are then introduced and the mixture is milled at 175–185 °C for 45–90 min. Rotor-tip speeds are typically held between 10 m/s and 18 m/s. The oil extension reduces the polymer-phase viscosity and accelerates particle-size reduction, allowing a storage-stable dispersed phase with a maximum particle size below 10 μm to be reached at lower specific energy input than with unextended SBS. The elastic recovery of the modified binder is commonly evaluated to ASTM D6084, with low-temperature ductility at 5 °C used as a secondary acceptance criterion.
Overheating above 200 °C promotes chain scission in the unsaturated polybutadiene midblock and causes a measurable loss in elastic recovery. Batch-to-batch variation in the asphalt source is more pronounced than variation in the polymer feed; therefore, the polymer dosage is normally fixed between 3.5 wt% and 4.5 wt% of the asphalt. Sulfur crosslinking is not required to build the SBS network because the styrene domains act as physical crosslinks, but if sulfur is later added to stabilize phase inversion, the addition must be kept low enough to avoid a sharp reduction in cold ductility. Production tanks require slow agitation after milling to prevent coalescence of the dispersed SBS-rich phase during storage at 160–170 °C.
Compounding in a co-rotating twin-screw extruder with an L/D ratio of 40:1 to 52:1 is run with a barrel profile from 120 °C in the feed zone to 170–190 °C at the die. The extension oil reduces the specific mechanical energy required to reach melt temperature, but it also lowers bulk density; forced side feeding may be required if the screw speed exceeds 400 rpm. Pre-drying is advisable when the pellets have been stored above 60% RH or chilled below dew point, because surface moisture can cause die foaming. Desiccant drying at 60 °C for 2 h is generally sufficient. If the melt temperature exceeds 220 °C, the unsaturated midblock undergoes thermo-oxidative degradation, visible as yellowing and a loss of tensile strength. In injection molding, the mold temperature should be kept below 40 °C to reduce sticking, and clamp force requirements are lower than those of unmodified polypropylene.
Formulators that replace an unextended SBS with Globalprene SBS 3741 should subtract the 37.5 phr extension oil from the external oil addition to avoid over-oiling. Because the extension oil is already distributed within the pellet, the compound reaches equilibrium hardness faster than a dry SBS-plus-oil mixture, but the external oil type can no longer be changed independently. The Shore A hardness after replacement is typically 8–12 points lower at the same total formulation oil content. This shift is measured with ASTM D2240-15 after conditioning at 23 °C and 50% RH for 24 h.
The grade is therefore selected for soft-touch grips, flexible footwear soles, and asphalt binders that must remain ductile at −20 °C, while higher-styrene grades are retained for rigid overmolding and structural adhesive applications. The unsaturated polybutadiene midblock creates an operational incompatibility with strong oxidizing acids, prolonged ozone exposure, and copper or manganese stearates, which can accelerate degradation. Carbon black, hindered-amine light stabilizer, or UV absorber addition is required for outdoor use. Incoming resin should be stored in unopened packaging below 30 °C; if MFR drift exceeds ±20% of the release value after prolonged storage, the material is quarantined for gel measurement before use.