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Dynasol Solprene® SBS 4320X

    • Product Name: Dynasol Solprene® SBS 4320X
    • Factroy Site: Yinchuan, Ningxia, China
    • Price Inquiry: sales8@ascent-chem.com
    • Manufacturer: Ascent Petrochem Holdings Co., Limited
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    Specifications
    HS Code 997539
    Polymer Type linear styrene-butadiene-styrene block copolymer (SBS)
    Appearance white to off-white porous crumb
    Styrene Content 30 wt%
    Diblock Content ≤1 wt%
    Density 0.94 g/cm3
    Mooney Viscosity ML 1+4 at 100 °C: 45 MU
    Melt Flow Rate 5 g/10 min at 200 °C/5 kg
    Shore A Hardness 75
    Tensile Strength 25 MPa
    Elongation At Break 700%
    Modulus At 300 Percent Elongation 3 MPa
    Volatile Matter ≤0.5 wt%
    Ash Content ≤0.2 wt%
    Antioxidant non-staining
    Form crumb

    As an accredited Dynasol Solprene® SBS 4320X factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Dynasol Solprene® SBS 4320X is packaged in 25 kg polyethylene-lined paper bags, 50 bags per 1,250 kg pallet.
    Container Loading (20′ FCL) Dynasol Solprene® SBS 4320X is loaded into a 20′ FCL container, palletized, kept dry, protected from moisture, and securely stowed.
    Shipping Dynasol Solprene® SBS 4320X is shipped as a non-hazardous thermoplastic elastomer in moisture-proof bags, boxes, or bulk containers on pallets. It is not regulated as dangerous goods for DOT, IMDG, or IATA and has no UN number. Keep dry, cool, and protected from contamination and direct sunlight.
    Storage Store Dynasol Solprene® SBS 4320X in a cool, dry, well-ventilated area away from direct sunlight, heat, sparks, and oxidizing agents. Keep original containers or bags tightly closed and palletized off the floor to prevent moisture and contamination. Avoid prolonged high temperatures and dust accumulation; follow local regulations and use appropriate PPE when handling.
    Shelf Life Dynasol Solprene® SBS 4320X typically has a 24-month shelf life when stored unopened in a cool, dry, well-ventilated area.
    Application of Dynasol Solprene® SBS 4320X

    Direct-injection footwear lines running two-colour PU/SBS midsoles require a styrenic rubber with enough melt strength to reproduce fine tread edges at a barrel set point no higher than 190 °C. Solprene 4320X is dry-blended with naphthenic oil, general-purpose polystyrene, and calcium carbonate before the mix reaches the injection screw. A starting compound for an outsole with Shore A 55–65 contains 4320X 100 phr, naphthenic oil 70–90 phr, general-purpose polystyrene 25–40 phr, calcium carbonate 10–20 phr, and a hindered-phenolic antioxidant at 0.5–1.0 phr. Direct-injection lines use screw L/D ratios of 18:1 to 22:1 with compression ratio settings below 2.5:1; excessive shear at the non-return valve overheats the compound above 200 °C and produces dark streaks at the weld-line. Finished soles are tested to ISO 20871:2018 for abrasion and ASTM D624 for tear strength, while flex resistance is assessed under ISO 17707:2005. Because footwear outsoles are consumer articles under Regulation (EC) No 1907/2006, the formulated compound must not exceed the applicable REACH Annex XVII restrictions for polycyclic aromatic hydrocarbons when extender oils are used; the oil producer should supply an EU-SVHC statement for mineral oil aromatics. On production lines, the main batch-to-batch variable is the oil-absorption capacity of the SBS crumb. If the volatile content exceeds 0.5 wt%, the first-stage dry blend can segregate and produce Shore A variation of ±4 points. Silicone-based mould-release agents that are applied at high frequency transfer to the sole surface and prevent subsequent bonding of PU sidewalls; when a two-material sole is specified, the SBS compound is buffed or plasma-treated before PU injection. Failure locations at the toe crease during flexing indicate inadequate blending of polystyrene rather than a deficiency of the block copolymer itself.

    What Limits Storage Stability When 4320X Is Dispersed in Oxidised Bitumen?

    In road-paving asphalt plants, the addition of Solprene 4320X to hot base bitumen follows a dispersion window that separates a stable polymer network from a gelled or phase-separated binder. The base bitumen is heated to 170–185 °C, and 4320X granules are metered into a high-shear mixer at 3.0–6.0 wt% for heavy-traffic polymer-modified bitumen; lower additions of 2.0–3.0 wt% are used only for workability modification and do not form a continuous elastomer network. High-shear dispersion at 3000–5000 rpm for 30–60 min converts the initial coarse granulometry into a swollen polymer-rich phase; paddle mixers that cannot exceed 1500 rpm leave visible SBS lumps and produce a binder with low elastic recovery after filtering. Where sulfur-based crosslinking is used, the sulfur addition must not exceed 0.05–0.15 wt% of the binder because higher levels create premature gelation and block the mill discharge screens. The finished PMB is graded under EN 14023:2010 using EN 13398:2018 elastic recovery and EN 13399:2018 storage stability; a top/bottom softening-point difference above 5 °C after 72 h at 180 °C indicates phase separation that cannot be corrected by additional stirring. The final product enters wearing-course asphalt mixes for high-shear roads, bus lanes, and port pavements.

    Control parameterStandard methodUse in PMA production
    Softening pointEN 1427:2015 / ASTM D36/D36M-14Top/bottom softening-point difference used for EN 13399:2018 storage stability
    PenetrationEN 1426:2015 / ASTM D5/D5M-20Low-temperature workability and PMB grade assignment
    Elastic recoveryEN 13398:2018 / ASTM D6084Continuous polymer network verification
    Storage stabilityEN 13399:2018Oven conditioning at 180 °C for 72 h
    ViscosityEN 13302:2018 / ASTM D4402Handling at 135 °C for pump and spray equipment
    Multiple stress creep recoveryAASHTO T350Permanent deformation at 0.1 kPa and 3.2 kPa

    Torch-Applied Membrane Formulations That Avoid Post-UV Surface Bleed

    Because torch-applied SBS-modified membranes are graded for low-temperature flexibility and heat ageing, the compounding vessel operates at a narrow shear gap to prevent agglomerated SBS domains from rupturing the polyester carrier. In this segment, 4320X is charged at 8–16 wt% into oxidised or distilled bitumen at 180–190 °C together with finely divided limestone or dolomite filler at 25–35 wt%; the polymer is swollen under high shear before the filler is fed. The finished binder is spread onto a polyester or glass-fibre carrier at a coating weight of 3.0–5.0 kg/m² and protected with a mineral or metal facing. Low-temperature flexibility of the membrane is assessed by bending at -15 °C to -20 °C under methods referenced in EN 13707:2009 and EN 13969:2009; the product must also tolerate the torch flame during installation without exposing the carrier. The main operating boundary is that prolonged compounding above 200 °C or repeated re-melting cycles oxidise the butadiene midblock and increase surface tack after UV exposure, which reduces the slip resistance of the installed roof.

    Formulating a hot-melt pressure-sensitive adhesive with 4320X at 145–160 °C begins with a resin-polymer solubility parameter check because the styrene endblock domains determine peel-to-shear balance. A starting label adhesive uses 4320X at 20–35 wt%, a C5/C9 hydrocarbon tackifier at 45–60 wt%, a naphthenic or paraffinic process oil at 15–25 wt%, and an antioxidant at 0.5–1.0 wt%; the resin is premelted in a sigma-blade mixer before the styrenic block copolymer is added under a nitrogen blanket. The molten adhesive is transferred through a heated filter and coated at 150–170 °C using a slot-die coater onto silicone release liner at coating weights from 20–30 g/m². Loop tack and peel are measured according to ASTM D6195 and ASTM D3330/D3330M, and the holding power data are generated under ASTM D3654/D3654M. For indirect food-contact packaging tape, the finished adhesive may be evaluated under FDA 21 CFR 175.105; the formulator must replace any free acrylic monomer source and verify that the process oil and tackifier do not exceed the migration limits established in the end-use specification. The limiting processing parameter is the viscosity drift after 8 hours at coating temperature: above 180 °C the unsaturated resin begins to form chromophores, and adhesive colour shifts to amber.

    When Twin-Screw Compounding Uses Polypropylene as the Continuous Phase

    In TPE-S compounds where 4320X is the elastomer phase and polypropylene forms the continuous matrix, phase inversion depends on the viscosity ratio at the mixing kneading blocks. The recommended starting formulation is 35–45 wt% Solprene 4320X, 15–25 wt% polypropylene homopolymer with an MFI of 10–25 g/10 min measured under ISO 1133-1:2022, 20–35 wt% naphthenic oil, and 0–20 wt% calcium carbonate or talc. A co-rotating twin-screw extruder with L/D 40:1 is operated with a barrel profile from 160 °C to 190 °C, side-feeding of filler, and oil injection into the molten section to avoid slip on the extruder root. Underwater pelletising is used because it preserves the surface hardness of the pellet and prevents re-agglomeration. The resulting TPE-S pellets are injection-moulded into automotive footmats, gear-shift bellows, and soft-touch interior grips; hardness is reported as ISO 48-4:2018 Shore A, tensile properties under ISO 37:2017, and melt volume-flow rate under ISO 1133-1:2022. If the compound is to be used in an enclosed cabin, fugitive emissions should be benchmarked against VDA 278:2016, and the oil selection must avoid low-molecular-weight fractions that condense on glazing. The main incompatibility occurs with polar flame-retardant masterbatches; halogen-free phosphate systems can plasticise the polystyrene endblocks and reduce the upper service temperature, although published data for this specific 4320X configuration is limited.

    Falling-Dart Impact in Extruded Styrenic Sheet: 4320X as a Rubber-Phase Diluent

    Extruded monolayer styrenic sheet for refrigerator liners and vending machine fascia uses a small addition of SBS 4320X to widen the processing window between gloss loss and stress-whitening. In a general-purpose polystyrene matrix, 4320X is pre-compounded as a masterbatch at 10–20 wt% and let down to 5–15 wt% in the final sheet compound; the twin-screw pre-compounding step uses a barrel profile between 190 °C and 210 °C and a residence time below 120 seconds because the styrene endblock begins to degrade above 210 °C. The sheet passes through a three-roll stack and is thermoformed into trays, clamshells, and appliance liners. Falling-dart impact is measured under ISO 6603-2, notched Charpy impact under ISO 179-1:2010, and tensile properties under ASTM D638-14. For food-contact thermoformed sheet, the finished article must comply with Regulation (EU) No 10/2011; the migration of butadiene, styrene, and low-molecular-weight oligomers must be measured after the thermoforming process because orientation can alter the diffusion path. The operational boundary is the high melt temperature of the polystyrene continuous phase: running below 190 °C causes the 4320X phase to remain undispersed and visible as gels, while running above 210 °C destroys the butadiene unsaturation and reduces the rubber toughening effect.

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    Certification & Compliance
    More Introduction

    Dynasol Solprene® SBS 4320X is a linear styrene-butadiene-styrene block copolymer supplied as a porous pellet or crumb. The product identifier separates it from oil-extended and low-molecular-weight grades in the Dynasol portfolio. Its bound styrene content is 30 wt%, with a specific gravity near 0.94 g cm⁻³ when determined according to ISO 1183-1. Melt flow rate at 190 °C under 5 kg load is typically below 1.0 g (10 min)⁻¹ when tested according to ISO 1133-1:2022 or ASTM D1238. The grade is not oil-extended, so the pellet surface remains porous but does not carry a paraffinic or naphthenic extender oil. This absence allows independent extender-oil selection but raises torque demand in low-shear mixers relative to oiled grades. The high molecular weight and controlled low diblock content produce a stronger physical network after styrene domains phase-separate from the polybutadiene continuous phase. On production-scale conveying systems, dense porous pellets are transferred with rotary airlock feeders; air velocities above 25 m s⁻¹ increase fines generation and require cyclone separation before dust enters the extruder throat. The CAS Registry Number for styrene-butadiene-styrene block copolymers is 9003-55-8.

    What Distinguishes 4320X from Radial SBS and Low-Molecular-Weight Linear Grades in Processing?

    The principal difference between Solprene SBS 4320X and radial 30 wt% styrene grades appears in the relationship between molecular architecture and viscosity. As a linear triblock, 4320X has two terminal styrene blocks connected by a polybutadiene midblock. At equal molecular weight, a linear chain dissolves faster and produces lower low-shear viscosity than a radial branched molecule. However, 4320X is a high-molecular-weight grade with controlled low diblock content, so its absolute melt flow rate remains below 1.0 g (10 min)⁻¹. On a capillary rheometer at 190 °C with a 1 mm die, the apparent shear viscosity may drop by roughly one order of magnitude when the shear rate increases from 10 s⁻¹ to 1000 s⁻¹. This shear-thinning response is typical of block copolymers with high styrene-domain cohesion. Compared with low-molecular-weight linear grades used in solvent adhesives, 4320X has lower melt flow but higher tensile strength and better high-temperature dimensional stability. The controlled low diblock fraction is important because diblock chains containing only one styrene block cannot form a load-bearing network; they plasticize the styrene domains and reduce tensile strength. Gel permeation chromatography data for 4320X show a narrow molecular weight distribution and low low-molecular-weight tail. These properties make the grade suitable for high-strength bituminous binders and compounded thermoplastic elastomers, but they also demand higher mixing energy in low-shear equipment.

    ParameterSolprene SBS 4320XRadial 30 wt% styrene SBSLow-molecular-weight linear SBS
    Molecular architecturelinearradiallinear
    Bound styrene30 wt%30 wt%30–31 wt%
    Melt flow rate at 190 °C/5 kg<1.0 g (10 min)⁻¹<1.0 g (10 min)⁻¹2–15 g (10 min)⁻¹
    Solution viscosity at 25 wt% in toluene2000–4000 mPa·s5000–8000 mPa·s<1000 mPa·s
    Asphalt storage stabilitymoderate to highhigherlower
    Primary applicationPMB, TPE compounding, footwearPMB, roofing membranesadhesives, low-viscosity PMB

    In bitumen modification, Solprene SBS 4320X is dispersed at 3–7 wt% into penetration-grade or viscosity-grade bitumen. High-shear rotor-stator mills or colloid mills are used after pellet pre-wetting in hot bitumen at 170–190 °C. The mixture is held in low-shear maturation tanks for 60–120 min until a continuous polymer-rich network forms. Under EN 14023, polymer-modified bitumens for paving are classified according to softening point, elastic recovery, and storage stability. Binders formulated with 4320X commonly raise the ring-and-ball softening point from 45 °C to 75–90 °C, depending on bitumen source and aromatic oil content. Elastic recovery at 25 °C according to EN 13398 can exceed 60%, and storage stability after 72 h at 180 °C under EN 13399 can show a softening-point difference below 5 °C. These values are not guaranteed because crude source, dispersion energy, and thermal history dominate the final morphology. The high molecular weight and controlled diblock level of 4320X improve high-temperature storage stability relative to low-molecular-weight linear grades, although a radial 30 wt% styrene grade may show a higher gelation threshold under quiescent storage. A production-scale failure observed in low-shear tanks is the formation of polymer-rich surface skins when pellets are added too quickly or when agitation stops prematurely; this is corrected by pre-milling the polymer into a bitumen concentrate at 12–15 wt% solids before letdown.

    When 4320X Is Compounded into Thermoplastic and Footwear Matrices

    When Solprene SBS 4320X is compounded with polypropylene or general-purpose polystyrene on a co-rotating twin-screw extruder with an L/D ratio of 32:1 to 40:1, barrel temperatures are normally set between 180 °C and 205 °C. Separate downstream feeding of the SBS pellets into the molten polypropylene after the first kneading block reduces thermal-oxidative degradation; simultaneous feeding may require the first two barrel zones to be run 10–15 °C lower to prevent pellet agglomeration on the screw root. The grade accepts paraffinic or naphthenic extender oil at 20–80 phr, but oil absorption is slower than with linear low-molecular-weight grades. When ambient relative humidity exceeds 60%, pellets are pre-dried at 70–80 °C for 2 h before extrusion to reduce steam splay and hydrolytic surface defects. In injection-molded footwear compounds, a formulation containing 25–35 phr 4320X, 15–25 phr polystyrene, 30–50 phr naphthenic oil, and 0.1–0.3 phr antioxidant typically produces Shore A hardness between 45 and 70 and tensile strength above 6 MPa when measured according to ISO 37. The hardness depends on oil content and styrene-domain continuity. On an injection molding machine with a clamping force of 800–1500 kN, melt temperature is held at 175–190 °C, injection speed at 20–50 mm s⁻¹, and holding pressure at 30–60 MPa. Maintaining melt temperature within ±5 °C of 180 °C is recommended during prolonged campaigns; larger deviations alter melt viscosity and part gloss.

    How Does 4320X Compare with Radial SBS and Linear Low-Molecular-Weight Grades in Solvent-Based Adhesives?

    In solvent-borne adhesive systems, radial 30 wt% styrene grades produce higher solution viscosity at equal solids than linear grades of similar molecular weight. Solprene SBS 4320X therefore dissolves faster and yields lower solution viscosity than a radial high-molecular-weight SBS, but its high molecular weight still requires longer dissolution and produces higher viscosity than low-molecular-weight linear adhesive grades. A 25 wt% solution in toluene at 25 °C may show a Brookfield viscosity in the range of 2000–4000 mPa·s, whereas a low-molecular-weight linear grade may remain below 1000 mPa·s and a radial grade may exceed 5000 mPa·s. In hot-melt pressure-sensitive adhesive formulations, 4320X contributes higher cohesive strength up to 50–60 °C than low-molecular-weight linear SBS but requires a higher processing temperature in sigma-blade mixers or screw-fed hot-melt units. Heat histories above 190 °C for more than 45 min can initiate gel formation; production melters use a nitrogen blanket and temperature interlocks. The styrenic domain dissolution temperature is approximately 95–100 °C, above which shear modulus declines. Probe tack and loop tack values must be measured according to ASTM D6195 or FINAT FTM 9; published data for specific 4320X-based adhesive formulations is limited, so pilot trials are required for exact rheology and tack values.

    Roofing and waterproofing membranes based on Solprene SBS 4320X are produced by dispersing the polymer into bitumen at 160–190 °C in a planetary mixer or high-shear mixer, followed by calendering or spreading onto a polyester or fiberglass reinforcement. The high molecular weight and low diblock content improve low-temperature flexibility and crack-bridging relative to oxidized bitumen or atactic polyolefin-modified membranes. Cold bending temperature can fall below −20 °C when the formulation includes sufficient compatibilizing aromatic oil and when compound thickness does not exceed 4 mm. Direct substitution of a low-viscosity linear SBS with 4320X without adjusting aromatic oil content can produce a viscosity increase that overloads low-torque mixers. A production-scale limitation observed on membrane lines is the appearance of polymer-rich specks when pellets are added faster than the mixer can incorporate them; pre-gelling in a side-arm extruder at 170 °C reduces this defect. The grade is not compatible with amine-based antistrip additives in wet bituminous systems; the combination can promote premature gelation and phase separation. Storage tanks are held below 180 °C under inert gas to limit oxidative degradation of the polybutadiene midblock. Membrane formulations are tested for tensile properties according to ASTM D6163 or EN 13956, and for low-temperature flexibility according to EN 1109. These values are formulation-dependent and do not reflect the raw polymer alone.

    Regulatory Compliance Matrix for Raw Polymer and Downstream Compounds

    Compliance is confirmed at the raw polymer level and must be re-evaluated for finished formulations. The following matrix lists the reference designations that typically govern SBS compounds in the applicable jurisdictions.

    Regulatory domainReference designationApplicability to raw 4320X
    EU chemical inventoryREACH Regulation 1907/2006Registered; downstream users must follow exposure scenarios
    EU classification and labellingCLP Regulation 1272/2008Not classified as hazardous in supplied form; SDS lists no SVHC above 0.1 wt%
    EU restriction of hazardous substancesRoHS Directive 2011/65/EU Annex IIApplies to finished electrical/electronic equipment; raw polymer not directly in scope
    US rubber articles for repeated use21 CFR 177.2600May apply to compounded rubber articles; final formulation must be confirmed
    US styrene block polymers21 CFR 177.1810Applicability limited; confirm for specific food-contact use
    Tensile and elongation testingISO 37 / ASTM D412Used for molded compound quality control
    Melt mass-flow rateISO 1133-1:2022Used for incoming resin control

    Operational boundaries for Solprene SBS 4320X are defined by thermal history, moisture, and chemical environment. Prolonged exposure to temperatures above 195 °C should be avoided because polybutadiene segments can undergo chain scission or oxidative crosslinking. Pellets stored at relative humidity above 60% require pre-drying before extrusion or injection molding. The polymer should not be combined with amine-based additives in wet bituminous systems, as premature gelation and phase separation have been observed on production-scale asphalt tanks. In halogen-free wire and cable compounds, the high molecular weight may require higher compounding torque than linear low-molecular-weight SBS; co-rotating twin-screw extruders with specific torque ratings above 10 N m cm⁻³ are preferred. The product is not intended for applications requiring direct FDA food-contact status unless the complete formulation is cleared under the relevant 21 CFR sections. The current manufacturer technical data sheet and safety data sheet remain the controlling documents for release limits and safe-use instructions.

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