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Kraton Kraton™D SBS D1494 P

    • Product Name: Kraton Kraton™D SBS D1494 P
    • Factroy Site: Yudu County, Ganzhou, Jiangxi, China
    • Price Inquiry: sales8@ascent-chem.com
    • Manufacturer: Ascent Petrochem Holdings Co., Limited
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    Specifications
    HS Code 283701
    Product Name Kraton D SBS D1494 P
    Polymer Type Linear styrene-butadiene-styrene (SBS) triblock copolymer
    Styrene Content 30 wt%
    Butadiene Content 70 wt%
    Form Powder
    Appearance White powder
    Specific Gravity 0.94
    Bulk Density Approx. 0.55 g/cm3
    Melt Flow Rate Approx. 10 g/10 min at 200 °C/5 kg
    Shore A Hardness 75
    Tensile Strength Approx. 30 MPa
    Elongation At Break Approx. 700%
    300 Percent Modulus Approx. 3 MPa
    Volatile Matter 0.5 wt% max
    Ash Content 0.2 wt% max
    Antioxidant Present

    As an accredited Kraton Kraton™D SBS D1494 P factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Packed in 25 kg multiwall paper bags, Kraton D SBS D1494 P is supplied as dusted porous pellets for convenient handling and storage.
    Container Loading (20′ FCL) 20′ FCL loaded with palletized Kraton™ D SBS D1494 P in dry, ambient conditions; secure stowage, no special ventilation, protect from moisture.
    Shipping Kraton™ D SBS D1494 P ships as a non-hazardous solid thermoplastic elastomer in sealed moisture-barrier bags, boxes, or bulk containers. It is not DOT/IMDG/IATA regulated. Keep dry, cool, and away from ignition sources; avoid dust generation and prolonged heat. Follow local rules and the SDS.
    Storage Store Kraton™D SBS D1494 P in a cool, dry, well-ventilated area away from direct sunlight, heat, sparks, and open flames. Keep containers tightly closed to prevent moisture ingress and contamination. Avoid contact with strong oxidizing agents. Maintain good housekeeping and protect pellets from prolonged UV exposure. Follow local regulations and the manufacturer’s SDS for specific temperature limits and shelf-life guidance.
    Shelf Life Typically 36 months from manufacture when stored dry in original packaging below 30°C, away from sunlight and moisture.
    Application of Kraton Kraton™D SBS D1494 P

    Kraton™ D1494 P, with a nominal bound styrene content of 31 wt% and a melt flow rate of 18 g/10 min at 200 °C/5 kg, is introduced into paving-grade bitumen at 3.5–5.5 wt% for dense-graded asphalt and at 6.0–8.0 wt% for bridge-deck waterproofing binders. The high-flow linear SBS grade and porous pellet morphology reduce dissolution time in the bitumen phase; dispersion is performed in a rotor-stator high-shear mill or in-line high-shear mixer at 170–185 °C for 60–90 min, with agitation speed maintained above 2,000 rpm until fluorescence microscopy indicates polymer domains below 5 µm. Compliance for the finished binder is documented against EN 14023:2010 (polymer-modified bitumen), ASTM D5976-96 (SBS-modified asphalt), ASTM D6084-18 (elastic recovery), ASTM D5/D5M-21 (penetration), ASTM D36/D36M-14 (softening point), AASHTO M 332 (performance-graded binders), and EN 13399:2016 (storage stability). Terminal products include hot-mix asphalt for high-traffic wearing courses, airport apron pavements, bridge-deck waterproofing membranes, and stress-absorbing membrane interlayers. At addition levels above 6 wt%, storage stability becomes the limiting parameter: unstabilized D1494 P-bitumen blends can show phase separation after 72 h at 165 °C in the EN 13399:2016 tube test, necessitating sulfur or reactive peroxide vulcanization at 0.08–0.15 phr to produce a stable PMB. The dynamic shear rheometer fingerprint under ASTM D7175-15 can be used to track the elastic recovery plateau and confirm the retention of the polymer network. Published data for this specific configuration in warm-mix asphalt at temperatures below 150 °C is limited because D1494 P melt viscosity may not fully wet mineral aggregates.

    For hot-melt pressure-sensitive adhesive compounding, D1494 P is metered at 20–35 wt% of the total adhesive formulation alongside a C5 aliphatic or C5/C9 mixed tackifier at 45–55 wt%, a naphthenic or white mineral oil at 10–20 wt%, and a hindered phenolic/phosphite antioxidant package at 0.5–1.0 wt%. The high flow of D1494 P allows a continuous twin-screw extruder with L/D 24:1 to 36:1 to operate at a flat temperature profile of 120 °C in the feed throat, 140–160 °C in the barrel, and 155–170 °C at the slot die, reducing thermal degradation of the polybutadiene midblock. Pre-drying at 70–80 °C for 2 h is recommended when storage relative humidity exceeds 60%. Compliance testing for the finished adhesive includes ASTM D3654-06 (loop tack), ASTM D3330/D3330M-04 (180° peel adhesion), ASTM D4498-07 (shear at 23 °C and 50 °C), and ISO 11339:2022 (T-peel for flexible-to-flexible laminates); for packaging tapes and labels, the formulation is evaluated under 21 CFR 175.105 where indirect food contact is required, and REACH Regulation (EC) No 1907/2006 applies to substances placed on the EU market. Terminal products include clear packaging tape, logistics labels, protective masking films, and hygiene article construction adhesives. The operational boundary for D1494 P in HMPSA is low-temperature flexibility: formulations containing more than 35 wt% polymer may show a decrease in loop tack below 5 °C due to the styrene domain modulus; published data for freeze-thaw cycling in this specific grade is limited.

    Injection Molded Footwear Soles and the Melt Flow Threshold of D1494 P

    For injection-molded footwear compounds, D1494 P is blended at 20–45 phr with general-purpose polystyrene at 15–25 phr, naphthenic oil at 10–20 phr, calcium carbonate or silica filler at 5–15 phr, and a stabilizer at 0.3–0.8 phr to create a high-flow TPE compound. The high melt flow allows direct injection into multi-cavity molds at barrel temperatures of 160–190 °C, with nozzle temperature held at 185–195 °C and mold temperature at 25–45 °C; clamp force requirements for a six-cavity unit sole mold are typically 80–150 tons depending on projected area. Compliance is established through ISO 20871:2018 (abrasion resistance), ISO 17707:2005 (flex cut growth), ASTM D395-18 (compression set), and REACH Regulation (EC) No 1907/2006; shoes intended for EU sale are assessed under Directive 94/11/EC for material labelling, not material safety alone. Terminal products include lightweight unit soles, midsoles, lugged outsoles, and slipper soles. At D1494 P loadings above 45 phr, the abrasion loss may exceed the ISO 20871:2018 limit for heavy-duty occupational footwear, so blends for such applications are modified with 5–10 phr of high-cis polybutadiene or low-MFI SBS. The processing window is bounded above by thermal degradation of the polybutadiene block at sustained barrel residence times exceeding 8 min at 200 °C; below 160 °C, incomplete plasticization causes surface melt fracture.

    Polypropylene impact modification uses D1494 P at 5–20 wt% in a PP homopolymer or block copolymer matrix, with optional linear low-density polyethylene at 5–10 wt% to enhance low-temperature impact. Compounding is performed on a co-rotating twin-screw extruder with L/D 32:1 to 40:1, screw speed 250–450 rpm, barrel temperature profile 185 °C in the intake zone increasing to 215–230 °C at the die, and melt temperature measured by infrared pyrometer at the die exit below 230 °C. The polybutadiene block is the limiting thermal component; sustained residence above 230 °C leads to gel formation and surface defects. Compliance for modified PP compounds is tested under ISO 179-1:2010/1eA (Charpy notched impact at 23 °C and −20 °C), ISO 178:2019 (flexural modulus), ASTM D256-23 (Izod notched impact), ISO 306:2022 (Vicat softening temperature), and RoHS Directive 2011/65/EU for electrical and electronic housings. Terminal products include automotive interior trim, appliance housing panels, luggage shells, and general-purpose injection-molded housewares. The addition of D1494 P above 20 wt% lowers flexural modulus by more than 30% relative to unfilled PP, which is acceptable only for soft-touch overmolded components; below 5 wt% the Charpy notched impact improvement at −20 °C is below 2 kJ/m² and may not justify the added compounding cost.

    What Limits Solvent-Borne Contact Adhesive Viscosity When D1494 P Replaces Low-MFI SBS Grades?

    For solvent-borne contact adhesives, D1494 P is dissolved at 15–25 wt% solids in a solvent blend containing toluene, methyl ethyl ketone, and acetone at 40:30:30 volume ratio, with terpene phenolic or rosin ester tackifier at 10–20 wt% of total solids. The high melt flow class of D1494 P reduces solution viscosity at equivalent solids compared with D1101-type SBS, enabling the use of 5–10 wt% higher solids while maintaining sprayability through air-atomized or airless equipment. Mixing is carried out in a closed sigma-blade mixer or high-speed disperser under a nitrogen blanket at 30–50 °C for 4–8 h; moisture ingress must be kept below 0.05 wt% because water vapor accelerates viscosity drift in ketone-containing systems. Compliance for the final adhesive is measured under ASTM D903-98 (peel strength of adhesive bonds), ISO 4587:2003 (lap-shear strength), ASTM D816-16 (contact adhesive properties), and Directive 2004/42/EC for VOC content limits in professional adhesives. Terminal products include footwear assembly adhesives, furniture laminate bonding, automotive headliner bonding, and construction panel adhesives. The neutral solvent system allows spraying at 0.3–0.5 MPa air pressure, but the high-MFI grade lowers green bond strength relative to low-MFI SBS; if a high initial grab is required, D1494 P is blended with 10–20 wt% of a low-MFI SBS grade. Avoid primary amine-functional silane additives because they promote discoloration and can destabilize the polybutadiene midblock in toluene solution.

    Self-adhered bituminous waterproofing membranes are produced with D1494 P at 6–12 wt% of the bitumen compound, plus aliphatic C5 tackifier at 5–10 wt%, calcium carbonate filler at 20–35 wt%, and a stabilizer at 0.3–0.5 wt%. The melt-blended compound is applied to a high-density polyethylene carrier film through a slot-die coater or calender at 160–180 °C, with coating thickness controlled between 0.6 mm and 1.5 mm and siliconized release liner applied inline. Compliance for the membrane is established under ASTM D1970-19 (self-adhering polymer-modified bituminous sheet for steep-slope roofing), EN 13969:2004 (flexible sheets for waterproofing), ASTM D4073-17 (bituminous materials at low temperatures), and EN 1928:2013 (watertightness). Terminal products include roof underlayments, below-grade foundation waterproofing, plaza deck membranes, and tunnel liners. The operational boundary is cold-temperature peel: formulations containing more than 10 wt% D1494 P may show reduced low-temperature adhesion below 0 °C unless the process includes post-application heat activation at 40–60 °C; published data for this specific grade in below-grade service at hydrostatic heads above 3 m is limited.

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    Certification & Compliance
    More Introduction

    Kraton™ D SBS D1494 P is a linear styrene-butadiene-styrene block copolymer supplied as a free-flowing powder. The polymer consists of polystyrene end-blocks connected by an unsaturated polybutadiene midblock. At ambient temperature, the polystyrene segments form glassy domains with a glass transition near 95 °C, while the polybutadiene phase remains elastomeric above approximately −85 °C. This two-phase morphology provides thermoplastic melt processability and elastomeric recovery without sulfur vulcanization. The powder designation indicates a porous particulate form suitable for direct addition to high-shear bitumen mixers, hot-melt adhesive vessels, and twin-screw compounding lines. Because the polybutadiene midblock is unsaturated, the material requires thermal stabilization during prolonged melt processing and is incompatible with strong oxidizing environments. The low molecular weight of the grade reduces melt and solution viscosity relative to higher-viscosity SBS products, but it also lowers cohesive strength and high-temperature viscosity build in final compounds.

    Typical supplier certificate-of-analysis parameters for this grade include bound styrene content of 30–32 wt%, total extractables below 1.0 wt%, volatile matter below 0.5 wt%, and ash below 0.2 wt%. The bulk density of the powder is commonly reported between 0.35 g/cm³ and 0.50 g/cm³. Melt mass-flow rate at 190 °C/5 kg falls in the 8–12 g/10 min range according to ISO 1133-1:2022 or ASTM D1238-20, and solution viscosity for 25 wt% polymer in toluene at 25 °C is typically in the 0.4–0.6 Pa·s range. These properties place the grade as a low-viscosity linear SBS. Lot-specific values supersede the typical ranges above, and the current supplier technical datasheet should be consulted for exact specification limits.

    Table 1: Characterization standards and typical audit thresholds for D1494 P
    PropertyTest standardTypical audit threshold
    Melt mass-flow rateISO 1133-1:2022 / ASTM D1238-208–12 g/10 min at 190 °C/5 kg
    Solution viscosityInternal capillary viscometry, 25 wt% in toluene at 25 °C0.4–0.6 Pa·s
    Tensile strength at breakASTM D638-14≥15 MPa
    Elongation at breakASTM D638-14≥700%
    Volatile matterISO 3251:2019≤0.5 wt%
    AshISO 3451-1:2019≤0.2 wt%

    What Distinguishes D1494 P from D1101 and D1155 in Molecular Architecture?

    The primary differences are molecular architecture, molecular weight, and bound styrene content. D1494 P is a linear triblock with low solution viscosity. D1101 is also a linear triblock but has substantially higher molecular weight, with solution viscosity near 4,000 mPa·s under the same 25 wt% toluene conditions. D1155 is a radial SBS with typical bound styrene content near 40 wt%, which raises hardness and tensile strength but reduces low-temperature elastic recovery relative to D1494 P. In melt processing, D1494 P generates lower die swell and lower melt strength than radial grades, making it less suitable for sheet extrusion where melt strength is critical. In solution or asphalt dispersion, the lower molecular weight enables faster dissolution and lower mixer torque, but it contributes less viscosity build per unit polymer loading.

    Table 2: Directional comparison of selected Kraton SBS grades
    ParameterD1494 PD1101D1155
    ArchitectureLinear triblockLinear triblockRadial (multiarm)
    Bound styrene content30–32 wt%30–32 wt%40 wt% typical
    Solution viscosity, 25 wt% in toluene at 25 °C0.4–0.6 Pa·s≈4.0 Pa·s4–5 Pa·s radial
    Melt flow rate, 190 °C/5 kg8–12 g/10 min<1 g/10 min<1 g/10 min
    Primary selection driversLow shear processing, high flow, asphalt and adhesivesHigher strength compounds, bitumen modification requiring high viscosity buildHigh modulus, high styrene asphalt and structural compounds

    The comparison is directionally supported by supplier product data, but grade-specific melt viscosity curves should be obtained before designing large-scale equipment. The radial architecture of D1155 introduces long-chain branching and higher melt elasticity, which increases die swell in profile extrusion and improves high-temperature rutting resistance in asphalt at the expense of greater shear heating during compounding. Published data for a direct D1494 P-to-D1155 substitution in all equipment configurations is limited, so pilot-scale verification is required where torque or melt-temperature limits are critical.

    In paving bitumen, D1494 P is typically incorporated at 3–7 wt% based on total binder mass. The bitumen is first dehydrated at 160–170 °C, then the powder is added to a rotor-stator high-shear mixer with tip speed between 15 m/s and 25 m/s. Dispersion is maintained at 175–185 °C for 45–120 min, depending on bitumen source and polymer loading. Complete dispersion is monitored by fluorescence microscopy according to ASTM D8079 or by torque stabilization on the production mixer. The modified binder is tested by softening point ASTM D36, penetration ASTM D5, elastic recovery ASTM D6084, and dynamic viscosity at 135 °C by ASTM D4402. At 4 wt% polymer addition, a typical paving bitumen with a base softening point of 46 °C may reach 62–68 °C, with penetration reduced from 70 dmm to 45–55 dmm and elastic recovery above 70% at 25 °C. The low-viscosity character of D1494 P shortens the torque peak during the dispersion inversion stage, but the plateau viscosity after complete dispersion is lower than that of D1101 at equal loading. Therefore, formulations targeting the same high-temperature performance grade may require 0.5–1.0 wt% additional polymer when substituting D1494 P for D1101. Storage stability of the modified binder should be evaluated according to EN 13399; top-bottom softening point differences above 2 °C typically indicate inadequate dispersion or insufficient compatibilization.

    For performance-graded asphalt specifications, the low-temperature stiffness and the high-temperature rutting parameter should be measured on the extracted binder using dynamic shear rheometry according to ASTM D7175. A D1494 P-modified binder with 4 wt% addition may fail the same high-temperature performance grade as a D1101-modified binder at equal loading because the lower molecular weight reduces the plateau modulus of the polymer-rich network. In dense-graded asphalt mixtures, the resulting impact on Hamburg wheel tracking and flow number should be confirmed by AASHTO T 324 and ASTM D8190 test programs. These mixture-level tests are required because binder-level softening point and elastic recovery do not fully predict rutting resistance under high tire-contact stresses at elevated pavement temperatures.

    When D1494 P Replaces D1101 in Hot-Melt Adhesives and Sealants

    Substitution is considered when the existing coating line operates at 150–180 °C and the higher melt viscosity of D1101 limits pump pressure or coating weight. A typical hot-melt pressure-sensitive adhesive formulation contains 30–40 wt% D1494 P, 35–50 wt% C5 or hydrogenated hydrocarbon tackifier, 15–25 wt% naphthenic oil, and 0.5–1.0 wt% hindered phenol antioxidant. Mixing is performed in a vertical change-can mixer or a continuous twin-screw extruder with L/D 40:1 and screw speed 300–500 min⁻¹. Melt viscosity at 177 °C is measured by ASTM D3236; D1494 P formulations typically show lower values than D1101-based compounds at equal polymer and tackifier loading, but the finished viscosity is strongly dependent on tackifier softening point and oil aromaticity. Peel strength on stainless steel is measured according to ASTM D1876, loop tack according to ASTM D6195, and high-temperature shear adhesion according to ASTM D3654. The lower melt viscosity reduces stringing and permits thinner coating weights on silicone release liner, but cohesive strength is lower. Therefore, the substitution is limited to tapes and labels where peel and tack dominate over high static load resistance. Published data for this specific formulation configuration is limited; laboratory coating trials with the target backing and release liner are required to confirm performance boundaries.

    In pressure-sensitive adhesive applications, the lower solution viscosity of D1494 P can shift the balance toward better wet-out on low-energy surfaces such as polyethylene and painted steel, but this wet-out advantage is coupled to lower shear holding power at 40 °C and 70 °C. The reduction in high-temperature adhesive performance is measurable by static shear test methods such as ASTM D3654 or AFERA 5012. If the adhesive is intended for automotive interior tapes with service temperatures above 80 °C, D1101 or a radial SBS should be retained unless the coating weight is increased or a high-softening-point tackifier is selected. Mixing hold time should be limited to 60–90 min at 170–180 °C because the unsaturated midblock can undergo oxidative chain scission and viscosity drift. A nitrogen blanket is recommended for continuous hot-melt tanks that operate unattended for more than 2 h.

    When formulated into construction sealants, D1494 P is used at 15–25 wt% with surface-treated calcium carbonate filler at 30–40 wt%, hydrocarbon resin, plasticizer, and stabilizer. The low melt viscosity supports application through meter-mix equipment at 150–170 °C and wetting of aluminum and primed concrete. Joint movement capability is evaluated by ASTM C719; movement capability below ±25% often indicates filler loading above the polymer network’s deformation limit. The use of amine-based adhesion promoters is not recommended because the unsaturated polybutadiene midblock can undergo premature viscosity build in the presence of basic species during hot storage. If filler loading exceeds 30 wt%, surface-treated calcium carbonate is required to limit moisture adsorption and dispersion defects. Pre-drying of the powder at 70–75 °C for 2–3 h is required when storage relative humidity exceeds 60%.

    Thermal Stability, Pre-Drying Requirements, and Storage Boundaries

    The polybutadiene midblock is susceptible to thermo-oxidative degradation at processing temperatures above 200 °C in air. In thermogravimetric analysis at 10 °C/min under nitrogen, the 5 wt% mass loss temperature is typically near 350 °C; in air, oxidative degradation can accelerate mass loss at lower temperatures. For hot-melt processing, the melt hold time should be limited to 60–90 min at 170–180 °C unless an inert gas blanket and antioxidant system are used. Oxidation induction time can be evaluated by ISO 11357-6. The powder should be stored in sealed containers below 35 °C and protected from UV irradiation. When conveyed through bulk handling systems, the powder may form combustible dust; the installation must be evaluated under NFPA 652 and the applicable European dust explosion protection requirements. Grounding and inerting are required when handling the fine fraction. Avoid storage and processing near strong oxidizers, organic peroxides, and unventilated hot surfaces.

    If the product remains in an open bin for more than 24 h at relative humidity above 70%, pre-drying at 75 °C for 2 h is recommended before melt processing, although the polymer is not hygroscopic in the manner of polyamide or polyester. The exact dust explosion parameters for this specific powder are not always published; site-specific dust testing is required before designing explosion venting or suppression systems. Bulk silo inventory should be rotated on first-in-first-out discipline, and extended storage beyond the supplier’s recommended shelf life should trigger re-testing of melt flow, volatile matter, and solution viscosity before release to production.

    Regulatory status depends on the production site and end-use region. Generic SBS block copolymers of this class are commonly listed on REACH, TSCA, DSL, IECSC, and KECI inventories, but the presence of the substance on any given inventory must be confirmed by the supplier for the specific grade and legal entity. For food-contact applications, compliance with FDA 21 CFR 172.175 or EU Regulation 10/2011 is not automatic and requires written grade-specific certification. The powder may produce respiratory nuisance dust at bag-dump stations; local exhaust ventilation and a dust mask are required where occupational exposure limits are approached. In continuous asphalt blending, a loss-in-weight gravimetric feeder with feed accuracy better than ±0.5% is necessary to prevent lot-to-lot feeding variation from changing the polymer-to-bitumen ratio.

    For impact modification of general-purpose polystyrene and polyolefin regrind, D1494 P is melt-compounded at 5–15 wt% on a corotating twin-screw extruder with L/D 40:1, using a barrel profile from 170 °C near the feed throat to 200 °C at the die. The low melt viscosity assists droplet breakup in a high-viscosity matrix, but the unsaturation reduces thermal stability in polypropylene systems processed above 230 °C. Notched Izod impact strength of polystyrene blends at 10 wt% loading is evaluated by ASTM D256-23; tensile properties are evaluated by ASTM D638-14. The addition of D1494 P generally improves impact strength by 1.5–2.5 kJ/m² over unmodified polystyrene while reducing tensile modulus by 10–20%. These shifts are smaller than those obtained with D1155 at the same loading because the radial architecture of D1155 imparts higher rubber-phase strength; however, D1155 also increases extruder torque and melt temperature. In injection molding of modified polystyrene, clamp force calculations should use melt viscosity at 220 °C and shear rates from 1,000 s⁻¹ to 10,000 s⁻¹. Mold cooling time is not substantially extended when the SBS loading remains below 10 wt%.

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