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Kraton Kraton™D SBS D4150

    • Product Name: Kraton Kraton™D SBS D4150
    • Factroy Site: Yudu County, Ganzhou, Jiangxi, China
    • Price Inquiry: sales8@ascent-chem.com
    • Manufacturer: Ascent Petrochem Holdings Co., Limited
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    VTB
    Specifications
    HS Code 565869
    Polymer Type Styrene-butadiene-styrene (SBS) block copolymer
    Molecular Structure Linear triblock
    Styrene Content 31 wt%
    Diblock Content 19 wt%
    Physical Form Pellets
    Specific Gravity 0.94
    Shore A Hardness 72
    Tensile Strength 27 MPa
    Elongation At Break 700%
    300 Modulus 3.5 MPa
    Melt Flow Rate 5 g/10 min at 200°C/5 kg
    Volatile Matter ≤0.5 wt%
    Ash Content ≤0.5 wt%

    As an accredited Kraton Kraton™D SBS D4150 factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Kraton™ D SBS D4150 is supplied in 25 kg moisture-resistant bags, with 1,000 kg bulk bags available for industrial shipment.
    Container Loading (20′ FCL) 20′ FCL loaded with Kraton™ D SBS D4150 in 25 kg bags on pallets, shrink-wrapped and containerized for export.
    Shipping Kraton™ D SBS D4150 is typically shipped as pellets/powder in sealed 25 kg moisture-barrier bags on pallets. It is non-hazardous and not regulated for transport by DOT, IMDG, or IATA. Ship/store cool and dry, away from direct sunlight and heat, with packaging kept sealed to prevent moisture pickup.
    Storage Store Kraton™ D SBS D4150 in a cool, dry, well-ventilated area away from direct sunlight, heat sources, sparks, and open flames. Keep containers tightly closed to prevent moisture and dust ingress. Separate from strong oxidizing agents. Avoid prolonged storage above recommended temperatures to prevent degradation or agglomeration. Use good housekeeping and follow SDS/local regulations.
    Shelf Life Kraton D4150 has a shelf life of 3 years from manufacture date when stored in original packaging under dry conditions.
    Application of Kraton Kraton™D SBS D4150

    In dense-graded asphalt paving, Kraton D4150, a linear styrene-butadiene-styrene block copolymer with nominal bound styrene near 30 wt%, is metered into hot penetration-graded bitumen at 3–7 wt%. The polymer-rich network forms after the system passes through its phase-inversion region. For similar linear SBS grades in Pen 60/70 bitumen, industrial rheology studies place that transition between 5 wt% and 7 wt%. Below the inversion loading the binder is bitumen-continuous. Above it the elastomer network contributes elastic recovery and high-temperature stiffness. The practical consequence is a measurable increase in softening point and a reduction in penetration at 25°C.

    The binder is blended in a low-shear tank at 160–170°C before passing through a colloid mill. A mill tip speed of 20–25 m/s is required to reduce the SBS domain size and develop the network. The milled binder is held in a stirred storage tank at 160–175°C. Storage time is kept below 24 h. Moisture trapped in the pellet feed is the main processing hazard. Drying at 70°C for 2 h is applied when storage relative humidity exceeds 60%. Foaming in the storage tank indicates residual moisture or incipient polymer degradation.

    The modified binder is classified under AASHTO M320 in North America and EN 14023 in Europe. Performance grade determination follows ASTM D6373 using a dynamic shear rheometer and a bending beam rheometer. Elastic recovery is measured under EN 13398. Multiple stress creep recovery is determined under ASTM D7405 at 64°C. Softening point is measured under EN 1427. The terminal binder is used in stone matrix asphalt, porous asphalt, and hot-mix asphalt for heavy-traffic intersections, bus lanes, and airport aprons.

    Oxidized bitumen for torch-applied roofing membranes requires a higher polymer loading than road paving because the sheet must survive torch installation without melt flow. Kraton D4150 is added at 8–12 wt% into oxidized bitumen. The compound is processed in a high-shear rotor-stator mixer at 170–190°C. A colloid mill is used for final dispersion. The blend is then cooled to 150–160°C for impregnation and coating of a glass or polyester carrier. The polymer network must survive the short thermal spike of torch-down installation, which reaches 150–200°C at the underside of the sheet.

    Product standards include EN 13707 for reinforced bitumen waterproofing sheets and ASTM D6162 for SBS-modified bituminous cap sheets. Low-temperature flexibility is checked under EN 1109 at −10°C or −20°C depending on climate class. Resistance to flow at elevated temperatures is assessed under EN 1110. Cap sheets are installed over insulation boards and base sheets. The D4150 network prevents bitumen flow from the reinforcement and reduces crack propagation at low service temperatures.

    Compliance and test method matrix for D4150 downstream applications
    Application segmentStandard or test methodCondition or parameter
    Polymer-modified road bitumenAASHTO M320Performance-graded binder
    Polymer-modified road bitumenASTM D7405MSCR at 64°C
    Roofing cap sheetASTM D6162SBS-modified bituminous sheet
    Roofing cap sheetEN 13707Reinforced bitumen sheet
    HMPSAFDA 21 CFR 175.105Incidental food contact adhesive
    HMPSAASTM D3236Melt viscosity at 160°C
    Footwear soleISO 815-1Compression set at 70°C / 24 h
    Footwear soleASTM D624Tear resistance

    What Limits Loop Tack and Shear Adhesion Failure Temperature When D4150 Is Compounded with C5 Resins?

    Hot-melt pressure-sensitive adhesives based on D4150 are typically formulated at 20–30 wt% polymer, 45–55 wt% aliphatic C5 hydrocarbon tackifier, and 15–25 wt% naphthenic or paraffinic process oil. The antioxidant package is held at 0.5–1.0 wt%. The linear SBS architecture provides melt processability and room-temperature elastomeric behavior. A C5 resin with a softening point of 90–110°C shifts the adhesive service temperature upward. Resin loadings above 55 wt% lower loop tack and embrittle the film. Oil loadings above 25 wt% reduce cohesive strength and can cause bleed-through on porous facestocks.

    Melt blending is performed in a corotating twin-screw extruder with an L/D ratio of 30:1 to 48:1. The feed zone is held at 120–140°C. The metering and die zones are set to 150–170°C. Vacuum venting at −0.08 to −0.09 MPa strips low-molecular-weight volatiles. Melt viscosity is determined under ASTM D3236 at 160°C and is maintained between 2,000 and 8,000 mPa·s for slot-die coating. Viscosity above 10,000 mPa·s causes die streaking and coating weight non-uniformity. Viscosity below 1,500 mPa·s causes strike-through on nonwoven substrates.

    Loop tack is measured under ASTM D6195. Peel adhesion is determined under ASTM D903 from stainless steel panels after 24 h dwell. Shear adhesion failure temperature is measured under ASTM D4498 at 500 g loading on a 25 mm × 25 mm overlap. Compliance for food-contact tapes and labels falls under FDA 21 CFR 175.105. The product is screened for REACH SVHC and RoHS restricted substances. Terminal products include pressure-sensitive label stock, masking tape, and nonwoven diaper closure tapes.

    Solvent-borne contact cements formulated with D4150 are prepared at 18–25 wt% total solids in a toluene–methyl ethyl ketone–n-hexane blend. The polymer-to-tackifier ratio is held between 1:0.5 and 1:1.2 using a C9 aromatic-modified hydrocarbon resin. Higher resin ratios reduce green strength. Lower resin ratios shorten open time below the working window needed for large-area panel lamination. The solution is mixed in a jacketed high-speed disperser at 25–35°C. Lump formation occurs when dry polymer is added without solvent circulation. Swelling precedes dissolution. The final viscosity is measured with a Brookfield viscometer at 20 rpm and adjusted to 1,500–5,000 mPa·s. The solution is filtered through a 100 µm bag filter before filling.

    Volatile organic compound content is controlled under EU Directive 2004/42/EC for non-aqueous adhesives. Bond strength is tested under ASTM D903 on canvas-to-plywood specimens after 24 h conditioning at 23°C and 50% RH. The measured room-temperature tack allows contact bonding without sustained clamping. End uses include furniture foam lamination, automotive headliner attachment, and shoe upper assembly. The formulated adhesive must be stored in sealed containers because solvent loss increases viscosity and raises the flash-fire hazard.

    Polybutadiene Vinyl Content and Processing Temperature Windows in D4150-Filled Sole Compounds

    Footwear sole compounds based on D4150 are dispersed in an internal mixer. A representative starting compound uses 100 phr D4150, 30–45 phr crystal polystyrene, 25–50 phr naphthenic oil, and 10–30 phr calcium carbonate. Crystal polystyrene raises Shore hardness. Naphthenic oil lowers melt viscosity. Calcium carbonate reduces shrinkage and improves dimensional stability. The compound is mixed at 130–150°C chamber temperature. Ram pressure is applied until the torque curve stabilizes. Dump temperature is kept below 160°C. The slab is cooled on a two-roll mill and granulated.

    Injection molding uses a reciprocating screw with barrel temperatures profiled from 155°C at the feed to 185°C at the nozzle. Mold temperature is maintained at 20–40°C. Injection pressure ranges from 60 to 100 MPa. Thermal degradation becomes rapid above 190°C because the polybutadiene mid-block crosslinks and embrittles. Below 155°C, the melt is too viscous to fill thin sole sections. The processing window is therefore constrained to 35°C. Melt flow rate is measured under ASTM D1238 at 190°C with 5 kg mass to verify batch consistency.

    Mechanical properties are tested under ASTM D412 for tensile properties and ASTM D624 for tear resistance. Compression set is determined under ISO 815-1 after 24 h at 70°C. Abrasion loss is measured under ISO 4649 Method A. Shore A hardness is determined under ASTM D2240 with a 3 s reading. End articles are injection-molded unit soles, wedge soles, and sheet stock for die-cut sock liners.

    When D4150 Is Melt-Blended with Polypropylene Homopolymer at 10–20 wt% during Extrusion

    Compounding D4150 with polypropylene homopolymer at 10–20 wt% creates a two-phase impact-modified blend. The PP matrix provides heat resistance. The SBS domains provide an energy-absorption mechanism. Compounding is performed in a corotating twin-screw extruder with 40:1 L/D. Barrel temperatures are set between 190°C and 210°C. The SBS and PP are both fed in the main throat. Below 180°C, the SBS domains remain incompletely melted. Above 220°C, the butadiene block degrades. A vacuum vent at −0.08 MPa removes residual moisture and low-molecular-weight volatiles.

    Notched Izod impact strength is evaluated under ASTM D256 at 23°C and −20°C. Tensile yield stress is measured under ASTM D638 at 50 mm/min. Published data for D4150 in this specific PP configuration is limited. End articles include automotive interior carriers, appliance housing components, and extruded profiles that require low-temperature ductility without solvent-borne adhesion systems.

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    Certification & Compliance
    More Introduction

    Kraton™ D4150 is a linear styrene-butadiene-styrene triblock copolymer supplied as a free-flowing powder. The macromolecular architecture consists of two terminal polystyrene blocks separated by a central polybutadiene segment; the polystyrene domains form reversible physical crosslinks at ambient temperature, while the unsaturated polybutadiene midblock supplies elastomeric recovery. Manufacturer-published representative data list a bound styrene content of 31 wt%, a specific gravity of 0.94 g/cm³ at 23 °C, and a Shore A hardness of 67 after 10 s on compression-moulded specimens evaluated according to ASTM D2240-15. Tensile properties determined on Type C die specimens under ASTM D412-16 at 500 mm/min include a representative tensile stress at break of 31 MPa and elongation at break of approximately 880%; the 300% tensile modulus is reported near 3.5 MPa. These values are indicative of a high-molecular-weight SBS grade whose unsaturated midblock requires thermal-oxidative stabilisation during any melt-processing operation.

    Morphological characterisation of solvent-cast and compression-moulded D4150 specimens by differential scanning calorimetry at 10 K/min under nitrogen reveals two principal thermal transitions: a polystyrene domain glass transition near 95 °C and a polybutadiene phase glass transition near −85 °C, with the transition temperatures confirmed by ASTM D3418-21. The phase-separated morphology is responsible for the product’s elastic recovery and for the temperature-dependent stiffness observed in formulated compounds. Because D4150 is supplied as a powder rather than a dense pellet, the available surface area for dry blending into bitumen, adhesive premixes, and plastisol formulations is higher than that of equivalent pelletised SBS grades; this physical-form difference materially affects feeding behaviour and dispersion kinetics on production-scale mixing equipment.

    What processing constraints govern D4150 in high-shear hot-melt adhesive compounding?

    In hot-melt adhesive compounding, D4150 is charged into sigma-blade mixers or co-rotating twin-screw extruders with a 40:1 L/D ratio alongside C5/C9 hydrocarbon tackifying resins and naphthenic extender oils. The melt temperature is maintained between 150 °C and 190 °C; sustained excursions above 200 °C initiate unsaturation-driven chain scission, gel formation, or colour build in the polybutadiene segment, particularly when heating times exceed 45 min under low-shear conditions. A hindered phenolic antioxidant with a phosphite secondary stabiliser is therefore incorporated at 0.1–0.3 wt% of the total compound, and the residence-time distribution is controlled by screw speed and feed rate. Production-scale failure modes include torque spikes when D4150 powder is introduced too rapidly into a partially filled mixing chamber, and the formation of undispersed polymer agglomerates when resin-oil wetting is insufficient in the first 20% of barrel length. Suppliers’ recommended formulations commonly employ tackifier loadings of 80–120 phr and extender oil loadings of 20–50 phr; melt flow rate is monitored by ISO 1133-1:2022 or ASTM D1238-20 for lot-to-lot consistency, although published data for this specific powder-feed configuration is limited and must be supplemented with in-house rheological data.

    In bitumen modification, D4150 is dry-blended into penetration-grade bitumen at addition levels of 3–6 wt% based on bitumen mass using an in-line high-shear colloid mill or an agitated high-torque tank at 170–185 °C. The polymer network that forms during high-shear dispersion raises the softening point and improves elastic recovery, with the exact softening-point increment dependent on base bitumen source, maltene-to-asphaltene ratio, and shear history. Softening point is measured by ASTM D36-14 ring-and-ball, penetration by ASTM D5/D5M-20, and low-temperature flexibility by ASTM D6084-18. Production-scale bottlenecks are frequently traced to insufficient tip speed in the colloid mill; when rotor tip speed falls below 20 m/s, polymer-rich agglomerates persist and storage-stable polymer-bitumen networks do not fully develop. The powder form of D4150 permits direct metered addition into the hot bitumen stream, eliminating the pellet-melting step required for pelletised SBS grades and reducing total mixing time in continuous plants. However, the same high surface area increases sensitivity to oxidative skin formation if the powder is held in a hot feed hopper without inert-gas blanketing.

    Rheological and morphological distinctions from D1101 and D1152.

    The principal difference between D4150 and D1101 lies in physical form and dispersion behaviour. D1101 is supplied as a dense pellet with a similar bound styrene content, whereas D4150 is a free-flowing powder that can be directly dry-blended into bitumen and adhesive premixes. The powder form reduces the energy required for initial polymer wetting but may increase hygroscopic surface adsorption. Compared with D1152, D4150 has a lower diblock content; this raises cohesive strength and shear resistance in pressure-sensitive adhesive systems while reducing room-temperature surface tack and low-energy substrate wetting. The difference is measurable by dynamic mechanical analysis: D4150-based adhesives typically display a higher plateau modulus above the polybutadiene glass transition and a more pronounced rubbery plateau than formulations based on higher-diblock SBS grades at equivalent resin and oil loadings. In bitumen modification, D4150 is selected where resistance to permanent deformation is required, while higher-diblock grades are selected where faster polymer dispersion and lower mixing viscosity are prioritised.

    Comparative grade-selection matrix based on physical form, composition, and primary processing route
    Attribute D4150 D1101 D1152
    Physical form free-flowing powder dense pellet pellet
    Bound styrene content 31 wt% 31 wt% 29.5 wt%
    Diblock content low low medium to high
    Primary processing route dry blending into bitumen; adhesive powder addition; plastisol modification melt compounding; footwear; general SBS modification adhesive and sealant formulations requiring aggressive tack
    Typical selection criterion direct powder addition and high cohesive strength general-purpose melt compounding high wetting and fast dispersion

    Shoe soling compounds formulated with D4150 are processed on single-screw extruders with a length-to-diameter ratio of 24:1 and a sheet die, with the powder form requiring pre-blending with minor amounts of antiblock or process oil to prevent screw starvation at feed throat temperatures above 40 °C.

    When D4150 replaces higher-diblock SBS in sealants and mastic formulations

    When D4150 replaces a higher-diblock SBS grade such as D1152 in a sealant or mastic formulation, the immediate process consequence is a rise in compound viscosity under low-shear mixing. The lower diblock content reduces the plasticising contribution of diblock molecules at the polybutadiene-styrene interface, so the mixer must be operated at elevated torque until the extender oil and tackifying resin migrate into the SBS network. Adhesion testing by ASTM D903-98 peel and ASTM D6195-03 loop tack generally shows lower initial tack for the D4150 compound, while ASTM D4498-07 shear adhesion failure temperature increases relative to higher-diblock formulations at comparable resin levels. This trade-off shifts the formulation toward structural mastics, high-shear adhesives, and bitumen-based sealants rather than aggressive pressure-sensitive labels. Formulators should avoid amine-based epoxy curing agents and strong oxidisers in D4150-containing solvent systems because the unsaturated polybutadiene segment can undergo premature crosslinking or chain scission during storage. Published data for this specific formulation configuration is limited; therefore, displacement studies should be performed on the intended production mixer rather than extrapolated from laboratory glassware.

    Storage and drying constraints are governed by the unsaturated polybutadiene segment and the powder form. D4150 should be stored in sealed original packaging below 40 °C, protected from ultraviolet exposure and ozone-generating equipment, and kept below 0.5 wt% moisture. If surface moisture exceeds this threshold, drying at 60 °C for 2 h in a dehumidified-air tray dryer is required before melt processing; extended exposure to ambient air at relative humidity above 60% can promote powder clumping and inconsistent gravimetric feeding. The product should not be blended with copper, manganese, or iron carboxylate catalysts that accelerate oxidative degradation of the unsaturation. In production-scale compounding, nitrogen blanketing of feed hoppers and use of medium-shear screw elements in the first mixing zone are effective controls for powder-induced feed instability and thermal history variation.

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