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Dynasol Solprene® SBS 4318

    • Product Name: Dynasol Solprene® SBS 4318
    • Factroy Site: Yinchuan, Ningxia, China
    • Price Inquiry: sales8@ascent-chem.com
    • Manufacturer: Ascent Petrochem Holdings Co., Limited
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    Specifications
    HS Code 374718
    Polymertype Linear styrene-butadiene-styrene block copolymer (SBS)
    Molecularstructure Linear triblock
    Styrenecontent 31 wt%
    Diblockcontent 18 wt%
    Density 0.94 g/cm³
    Meltflowrate 5 g/10 min at 200 °C/5 kg
    Shoreahardness 75
    Tensilestrength 22 MPa
    Elongationatbreak 700%
    Modulusat300percent 3.0 MPa
    Volatilematter ≤0.5 wt%
    Ashcontent ≤0.2 wt%
    Appearance White to light yellow porous crumb
    Antioxidant Non-staining

    As an accredited Dynasol Solprene® SBS 4318 factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Dynasol Solprene® SBS 4318 is supplied in 25 kg polyethylene-lined paper bags, typically palletized for safe industrial storage and transport.
    Container Loading (20′ FCL) 20′ FCL container loaded with Dynasol Solprene® SBS 4318 in sealed bags, palletized and secured for overseas transport.
    Shipping Dynasol Solprene® SBS 4318 is shipped as a non-hazardous solid styrenic block copolymer. It is not regulated for transport under DOT, ADR/RID, IMDG, or IATA; no UN number, hazard class, or packing group applies. Keep dry and avoid excessive heat during handling and storage.
    Storage Store Dynasol Solprene® SBS 4318 in a cool, dry, well-ventilated area away from direct sunlight, heat, ignition sources, moisture, and oxidizing agents. Keep containers tightly closed and protect from contamination. Avoid excessive temperatures and prolonged UV exposure. Follow first-in, first-out stock rotation. Store only in original or compatible containers, ensuring adequate ventilation and spill containment.
    Shelf Life Dynasol Solprene® SBS 4318 typically has a 24-month shelf life when stored unopened in a cool, dry, well-ventilated area.
    Application of Dynasol Solprene® SBS 4318

    Bituminous paving applications that require PG 76-22 or PG 70-28 continuous grade under AASHTO M 332 achieve the necessary high-temperature stiffness and low-temperature relaxation by pre-swelling Solprene SBS 4318 into paving-grade bitumen at 4.0–6.5 wt% of the bitumen phase. The linear triblock architecture of Solprene SBS 4318, with approximately 31 wt% bound styrene, determines the percolation threshold for a continuous elastic network. At additions below 4.0 wt%, the styrenic endblock network does not reach percolation; the resulting binder displays a phase angle above 75° at 10 rad/s and 64°C under ASTM D7405-20, indicating viscous character rather than elastic recovery. High-shear dispersion is performed in a colloid mill or in-line high-shear mixer at 170–185°C with rotor-tip speeds of 20–25 m/s and residence times of 60–120 min. Bitumen sources with high asphaltene content above 10 wt% can require lower SBS loadings because asphaltenes interact with the butadiene midblock and amplify the polymer network. The formulation often includes 3–6 phr of heavy naphthenic or aromatic process oil to depress binder viscosity below 3.0 Pa·s at 135°C, which is the maximum practical pumping viscosity for road paving equipment under EN 14023. Storage stability is measured as the difference in softening point between the top and bottom of an oven tube after 72 h at 160°C under ASTM D7173-21; a ΔT below 2.5°C is required for most European motorway tenders, and this corresponds to polymer particle sizes below 10 μm. Terminal products include stone mastic asphalt for heavy-traffic corridors, open-graded friction course for wet-weather runoff, and bridge-deck waterproofing mastic asphalt. Equipment with electric heating rods must be calibrated to avoid wall temperatures above 200°C, because oxidative degradation of the butadiene midblock causes a loss of elastic recovery after thin-film oven ageing under ASTM D1754-14 of more than 15%.

    SBS 4318 addition (wt%)Softening point (°C, ASTM D36)Elastic recovery at 25°C (%, EN 13398)Storage stability ΔT (°C, ASTM D7173-21)
    3.048–5535–501.0–2.0
    4.555–6555–701.5–3.0
    6.065–7865–852.0–4.0
    7.578–9275–903.0–5.0

    Why Does Closed-Pan Mixing Produce More Uniform Hot-Melt PSA Than Single-Screw Extrusion?

    Adhesive converters using Solprene SBS 4318 in hot-melt pressure-sensitive coatings should set the elastomer loading at 20–35 wt% of the total adhesive, with 45–55 wt% tackifying resin and 10–25 wt% naphthenic or paraffinic process oil. A 25/52/23 elastomer/resin/oil mass ratio produces loop tack of 18–25 N/25 mm under ASTM D6195-03 at 300 mm/min, but the value falls below 10 N/25 mm if more than 22 wt% oil is used because the oil preferentially swells the butadiene midblock and forces the tackifier into the polybutadiene phase. Closed-pan mixing in a heated sigma-blade mixer at 145–165°C for 45–90 min under nitrogen generates a homogeneous melt without the high-shear hot spots that occur in single-screw extruders, where SBS 4318 exhibits elongational viscosity peaks and possible melt fracture at screw speeds above 80 rpm. Twin-screw operations are permissible with side-fed tackifier at an L/D of 40:1 and vacuum devolatilization at -0.08 MPa, but barrel setpoints must remain at 150–170°C. The terminal products are carton-sealing tapes, laser labels, and nonwoven hygiene positioning tapes. Compliance is evaluated under FDA 21 CFR 175.105 for indirect food-contact adhesives, European REACH Annex XVII restrictions on PAH content in extender oils, and ASTM D3330-04 peel adhesion at 180° and ASTM D3654-82 shear adhesion failure temperature. Migration resistance is tested by contact staining under ISO 3865 at 60°C for 72 h; formulations exceeding 22 wt% paraffinic oil form a continuous surface film and are rejected for coated paper face stocks.

    Injection-Moulded Sole Compounds and Abrasion Performance Under DIN 53516

    In injection-moulded sole production, Solprene SBS 4318 is compounded at 40–60 phr as the primary elastomer, blended with general-purpose polystyrene at 20–35 phr, naphthenic oil at 5–15 phr, and an antioxidant package. The compound is dry-blended in a high-speed mixer at 70–80°C until the oil is absorbed by the porous crumb, then melt-compounded in a co-rotating twin-screw extruder at 150–180°C with screw speeds of 200–350 rpm and pelletised under water. Injection moulding uses barrel temperatures of 160–195°C, nozzle temperature of 185–200°C, and mould temperature of 25–40°C; clamp force for multi-cavity sole moulds is typically 800–1,200 kN. The residence time must not exceed 8 min at 190°C because butadiene blocks degrade and cause surface splay and a drop in tear strength measured under ISO 34-1:2022. A 40 phr SBS 4318 compound reaches 65–70 Shore A hardness, while a 60 phr loading produces 55–60 Shore A; abrasion loss under DIN 53516 is typically 200–250 mm³, which is acceptable for casual soles but not for safety footwear outsoles requiring EN ISO 20345 abrasion performance. Terminal products are unit soles, wedge soles, and children’s casual footwear. REACH SVHC screening and California Proposition 65 aromatic hydrocarbon limits apply. The grade must not be blended with amine-based stabilizers because discoloration and changes in ASTM D395-18 compression set may occur after UV exposure at 0.55 W/m² for 200 h.

    In membrane waterproofing, a controlled phase inversion occurs only when 8–12 wt% Solprene SBS 4318 is pre-swollen into oxidised or distilled bitumen at 130–150°C for 30 min before high-shear dispersion at 170–180°C in a multi-blade planetary mixer. The mixing endpoint is defined by a softening point rise of 35–45°C above the base bitumen and by the disappearance of visible SBS particles under microscope at 100×. The compound is filled with 20–30 wt% limestone or talc, stabilised with 0.1–0.3 wt% antioxidant, and calendered onto a polyester or fiberglass carrier at 110–130°C; roll pressure is adjusted to maintain carrier penetration without tearing. A 10 wt% SBS loading passes EN 1109 cold bend at -15°C, while 12 wt% is typically required for -25°C in torch-on membranes with heat resistance above 100°C under EN 1110. Conformity is assessed under EN 13707 for reinforced bitumen sheets for roofing, EN 1928 for watertightness, and ASTM D6164 for SBS-modified bituminous membrane systems in North American specifications. Terminal products include below-grade foundation membranes, tunnel liners, and bridge-deck waterproofing. Roll temperatures above 135°C during calendering cause orientation-induced shrinkage above 2% in the carrier and must be avoided; copper naphthenate-based biocides should not be added to SBS-modified bitumen because network destabilisation can lower heat resistance by more than 15°C after 12 weeks at 80°C in EN 1296 ageing tests.

    When SBS 4318 Is Introduced into Polystyrene-Rich Masterbatches

    Polystyrene toughening with Solprene SBS 4318 is viable only when the rubber particle size is maintained between 0.5 μm and 2.0 μm; this is achieved by blending 10–25 wt% SBS into general-purpose polystyrene or high-impact polystyrene at melt temperatures of 180–210°C in a counter-rotating twin-screw extruder with L/D 36:1 and atmospheric or vacuum devolatilization. The screw configuration includes two kneading blocks and a downstream injection port for 1–3 phr of liquid paraffin to control shear heating. Process stability is the limiting factor: if residence time above 200°C exceeds 45 s, butadiene degradation generates gel specks and reduces notched Izod impact strength by 20–30% when measured under ASTM D256-23. At 15 wt% SBS 4318, a general-purpose PS homopolymer with a notched Izod of 15–20 J/m can be raised to 70–90 J/m; at 25 wt% loading, values of 100–130 J/m are attainable but tensile modulus falls by approximately 15% compared with the unmodified resin under ASTM D638-14. Terminal products are rigid packaging trays, appliance housings, and audio-visual component covers where optical clarity is not critical because the SBS reduces light transmittance below 85% at 2 mm thickness. Regulatory compliance for food-contact articles follows FDA 21 CFR 177.1640 for polystyrene and EU 10/2011 migration limits only when the specific SBS grade and processing stabilisers meet residual monomer limits; published data for this specific Solprene SBS 4318 configuration in food-contact PS masterbatches is limited and requires migration screening under the final application.

    For solvent-borne construction sealants, Solprene SBS 4318 is dissolved at 15–30 wt% in mineral spirits or a toluene/hexane blend with 20–35 wt% hydrocarbon tackifier and 0.5–1.5 wt% fumed silica thixotrope. The production process is a high-speed cowles dissolver operating at tip speeds of 6–12 m/s for 60–90 min; solvent is added in two stages to avoid dry agglomeration and excessive shear heating above 40°C. The sealant is extruded through a gunnable cartridge and skins over within 15–30 min at 23°C and 50% RH, with full cure by solvent release rather than moisture. Terminal products are roof penetration seals, construction joint fillers, and weatherproofing sealants for metal buildings. Compliance is assessed under ISO 11600-1:2014 for joint sealant classification, ASTM C920-18 for elastomeric joint sealants where applicable, and REACH restrictions on toluene and PAH content in solvent blends. The addition of solvent should not exceed 35 wt% because the final sealant shrinks more than 12% by volume and can lose adhesion to porous concrete after 1,000 h of UV exposure under ISO 105-B02.

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    Certification & Compliance
    More Introduction
    Solprene® SBS 4318 is a linear styrene-butadiene-styrene block copolymer supplied as low-odour solid pellets for compounding, hot-melt and solvent-borne adhesives, footwear, and polymer modification. The grade belongs to the Dynasol Solprene 43xx series and is specified as an unextended SBS elastomer; no extender oil is incorporated in the pellet. Bound styrene is controlled in the 30–32 wt% band, which places the morphology in a low-styrene thermoreversible network regime rather than a high-styrene glassy reinforcement regime. Specific gravity measured by ISO 1183-1:2019 lies between 0.93 and 0.95; volatile matter determined by ASTM D5668 is typically below 0.5 wt%. The low-styrene structure limits hardness at room temperature but permits high extension before break when tested per ASTM D412-16. Because the midblock contains unsaturation, oxidative stabilization and ultraviolet protection must be designed into the final compound; published data for this specific configuration is limited, so qualification trials should use the current manufacturer certificate of analysis.

    Does the Linear Architecture of SBS 4318 Shift Melt Elasticity Relative to Radial SBS?

    Molecular architecture determines melt elasticity, die swell, and low-shear viscosity more than single-point melt mass-flow rate. SBS 4318 is a linear triblock with a lower concentration of high-molecular-weight gel than radial SBS grades of similar styrene mass fraction. In a co-rotating twin-screw compounding extruder with 40:1 L/D and segmented kneading blocks, the linear grade typically reaches stable head pressure with 15–20% lower specific energy input than a radial SBS of equivalent styrene content at 250–300 kg/h; this observation derives from production-scale lines and should not be interpreted as a universal rule. A single-point melt mass-flow rate test at 200 °C/5 kg per ISO 1133-1:2022 shows higher flowability for the linear grade than for high-molecular-weight radial controls, but die design requires capillary rheometry across 100–1000 s⁻¹. The shear-thinning exponent and entrance pressure drop are needed because SBS melts are highly elastic; gate freeze-off and die swell can differ by 20–40% between linear and radial grades at the same MFR.

    PropertyRepresentative rangeTest method
    Bound styrene30–32 wt%Manufacturer internal FTIR/NMR
    Volatile matter≤ 0.5 wt%ASTM D5668
    Ash≤ 0.5 wt%ISO 247:2006
    Specific gravity0.93–0.95ISO 1183-1:2019
    Melt mass-flow rate5–15 g/10 minISO 1133-1:2022, 200 °C/5 kg
    Tensile strength at break15–22 MPaASTM D412-16, Die C
    Elongation at break600–800%ASTM D412-16, Die C
    300% modulus1.8–3.0 MPaASTM D412-16, Die C
    Hardness70–85 Shore AASTM D2240-15
    Solution viscosity, 25 wt% in toluene at 25 °C0.8–2.5 Pa·sBrookfield, ISO 2555

    These ranges are representative of industrial lot-release data, not a specification. Tensile properties are sensitive to compression molding temperature and cooling rate; ASTM D412-16 Die C specimens should be conditioned at 23 ± 2 °C and 50 ± 5% RH for 40 h before testing. Coupling efficiency and styrene block length distribution influence hysteresis and tension set; these are not captured by single-point hardness or MFR. For incoming inspection, a compounding plant should measure lot-to-lot melt mass-flow rate, volatile matter, and solution viscosity before releasing the material to production. Storage in a dry, ventilated warehouse below 40 °C extends oxidative stability; inventory rotation should follow first-in-first-out because butadiene unsaturation continues slow oxidation even in pellet form. Regulatory conformity, including REACH registration under EC 1907/2006 and RoHS Directive 2011/65/EU, must be confirmed from the current safety data sheet; no exemption should be assumed.

    Bitumen Modification and High-Shear Processing

    Polymer-modified bitumen with SBS 4318 is manufactured by dispersing 3–6 wt% polymer into bitumen at 170–190 °C using a rotor-stator high-shear mill or a low-shear anchor mixer with external recirculation. The processing window is narrow: below 170 °C, the SBS phase does not swell and form a continuous network; above 195 °C, thermo-oxidative chain scission rapidly reduces complex modulus and phase separation appears. The practical upper limit is therefore held within a ±5 °C band around 190 °C. In a 2–4 t asphalt blend unit with a 15–20 kW rotor-stator mill, homogeneous morphology is typically achieved after 90–150 min at 180 °C; the exact time depends on maltene/asphaltene ratio and pellet porosity. Addition below 3 wt% may produce dispersed SBS droplets rather than a continuous network, with little improvement in softening point; addition above 7 wt% creates a viscosity cliff that limits pumping and spray application. Storage stability is evaluated by EN 13399:2017 or ASTM D7173; a softening-point difference between top and bottom samples of less than 5 °C is commonly required for polymer-modified bitumen. Batch-to-batch variance in SBS pellet porosity affects wetting and dispersion time more than final ring-and-ball softening point. Nitrogen blanketing of storage tanks and a maximum hold time of 4 h at 180 °C reduce oxidative degradation.

    For injection-molded footwear units, SBS 4318 compounds with Shore A 70–85 are processed on machines with 350–450 t clamp force and screw L/D 20:1–25:1. Barrel zone temperatures from feed to nozzle are usually 150/160/170/175 °C; mold temperature is kept at 25–45 °C. Gate velocities above 500 mm/s can induce surface melt fracture and knit-line delamination in SBS-rich formulations. Cycle time is affected by the need to purge the screw with polystyrene or a low-MFR SBS after each production run. Pre-drying at 60–70 °C for 2–4 h is required when storage relative humidity exceeds 60%; moisture uptake above 0.1 wt% causes splay and surface defects in molded parts. Indoor footwear formulations typically use 0.1–0.3 wt% of a hindered phenolic/phosphite antioxidant blend; outdoor soles require additional UV stabilizers because the butadiene midblock is susceptible to ozone cracking. Compounds may be sulfur-vulcanized in the butadiene phase when blended with natural rubber or butadiene rubber; vulcanization kinetics are measured by moving-die rheometer per ASTM D5289-19a at 160 °C, but the polystyrene domains remain physically crosslinked. Mold shrinkage is measured on plaque tools per ASTM D955-21 and is generally anisotropic.

    Solvent-borne adhesive formulations based on SBS 4318 are dissolved at 15–25% solids in a toluene/ethyl acetate/hexane blend using high-shear blade agitation; solution viscosity is checked by ISO 2555 at 20 °C. Peel adhesion to stainless steel per ASTM D6862 requires 10–30 phr of a C9 tackifying resin with softening point 90–110 °C. For hot-melt adhesives, SBS 4318 is melt-blended at 150–170 °C with resins and oils in sigma-blade or screw mixers; pot life is limited by thermo-oxidative crosslinking above 180 °C. Ketones and chlorinated solvents should be avoided when stored in unlined steel drums because water absorption above 0.1 wt% reduces tack. Free amine-based process aids should be avoided in high-temperature mixing above 180 °C; they can promote discoloration and reduce storage stability.

    In polypropylene, SBS 4318 is introduced at 5–15 wt% as an impact modifier. Notched Izod impact per ISO 180:2019 improves only when the SBS phase is dispersed below 2 µm; therefore, a co-rotating twin-screw extruder with 40:1 L/D and downstream feeding is used. Avoid melt contact with polyamide above 240 °C because oxidative degradation of the butadiene segment generates acidic species. In polystyrene blends, 10–20 wt% SBS 4318 raises elongation at break from below 2% to 25–60% depending on gate orientation and specimen direction; tensile tests are conducted per ASTM D638-14. The improvement is highly anisotropic, and cross-direction specimens may show lower gains. Migration of low-molecular-weight oils from the compound above 60 °C should be assessed by ASTM D1203-21 if dimensional stability or surface tack is critical.

    When the Compound Demands Lower Solution Viscosity than a Lower-Flow Linear SBS Control

    Compared with a lower-flow linear SBS of similar styrene content, SBS 4318 typically shows lower solution viscosity at 25 wt% in toluene and higher MFR at 200 °C/5 kg, which reduces solvent retention in adhesive films and shortens injection-molding cycle time. The trade-off appears in hot tensile strength and creep resistance above 60 °C. Compression set measured by ASTM D395-18 Method B after 70 °C/24 h is typically higher for the lower-viscosity grade, making it unsuitable for applications requiring ≤ 60% compression set under those conditions without blending with radial SBS or partial replacement by SEBS. Differences from radial SBS grades are most visible in low-shear melt elasticity, lot-to-lot gel content, and solvent dissolution time; differences from oil-extended SBS grades appear in formulation latitude because downstream oil addition is not constrained by a preloaded extender. The choice between SBS 4318 and higher-molecular-weight SBS should therefore be governed by end-use temperature and allowable permanent set, not by MFR alone.

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