| HS Code | 923462 |
| Product Name | Kraton™ D SBS D1493 P |
| Polymer Type | Styrene-butadiene-styrene (SBS) block copolymer |
| Polymer Architecture | Linear triblock |
| Styrene Content | 30 wt% |
| Butadiene Content | 70 wt% |
| Physical Form | Powder |
| Color | White |
| Density | 0.94 g/cm³ |
| Melt Flow Rate | 10 g/10 min at 200°C/5 kg |
| Tensile Strength | 25 MPa |
| Elongation At Break | 700% |
| Shore A Hardness | 70 |
| Volatile Matter | ≤0.5 wt% |
| Packaging | 25 kg bags |
As an accredited Kraton Kraton™D SBS D1493 P factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Kraton™ D SBS D1493 P is supplied in 25 kg moisture-barrier paper bags, palletized with 40 bags per pallet. |
| Container Loading (20′ FCL) | Kraton™ D SBS D1493 P is loaded in a 20-foot FCL container, securely palletized and restrained for safe ocean transport. |
| Shipping | Kraton™ D SBS D1493 P is shipped as non-hazardous polymer pellets in moisture-resistant bags or boxes. Store and transport in a cool, dry, ventilated area away from direct sunlight, heat, and ignition sources. It is not classified as dangerous goods; standard freight and handling apply. |
| Storage | Store Kraton D SBS D1493 P in a cool, dry, well-ventilated area away from direct sunlight, heat, ignition sources, and strong oxidizers. Keep original packaging closed to prevent moisture and contamination. Protect from ozone and physical damage; avoid prolonged high-temperature exposure. Use first-in, first-out stock rotation and handle according to the safety data sheet and local regulations. |
| Shelf Life | Kraton D SBS D1493 P has a typical 24-month shelf life when stored cool, dry, and in sealed original packaging. |
Where road-paving bitumen requires a continuous polymer network, Kraton™ D1493 P is added at 4.0–5.5 wt% to penetration-grade binders such as 50/70 or 70/100 preheated to 160–170°C. Dispersion is carried out in an inline high-shear mill, typically a Siefer Trigonal or IKA Works DISPAX reactor, with rotor tip speeds of 18–25 m/s and outlet temperature controlled at 175–190°C. After the polymer addition, the binder enters a low-shear maturation tank for 45–90 min; this dwell period enables swelling of the butadiene midblock and formation of a styrene end-block physical network. Without sufficient maturation, the modified binder fails elastic recovery testing because the continuous polymer phase remains incompletely developed. European binder compliance follows EN 14023:2010 with base bitumen conformity to EN 12591, while United States works specifications use AASHTO M320 and ASTM D5976. Laboratory verification includes softening point by ASTM D36, penetration by ASTM D5, elastic recovery by EN 13398, and storage stability as the difference in softening point after 72 h at 163°C. Terminal products are polymer-modified bitumen binders for stone mastic asphalt wearing courses, stress-absorbing membrane interlayers, airport runway overlays, and pumpable crack sealants. A production-scale boundary appears when the polymer dose falls below approximately 3.0 wt%; in that case the SBS phase remains dispersed as discrete islands rather than a load-bearing fibril network, and the material behaves mainly as thickened bitumen during fatigue loading.
| D1493 P addition | Softening point ASTM D36 | Penetration ASTM D5 | Elastic recovery EN 13398 | Storage stability ΔSP 72 h/163°C |
|---|---|---|---|---|
| 2.0 wt% | 52–58°C | 70–85 dmm | 45–60% | ≤2.5°C |
| 4.0 wt% | 60–68°C | 55–70 dmm | 65–80% | ≤3.0°C |
| 6.0 wt% | 68–78°C | 45–60 dmm | 75–90% | ≤4.0°C |
| 8.0 wt% | 78–88°C | 35–50 dmm | 80–95% | ≤5.0°C |
At 160–180°C in a jacketed sigma-blade mixer or co-rotating twin-screw extruder, hot-melt pressure-sensitive adhesives based on Kraton™ D1493 P are compounded with 18–25 wt% SBS, 45–55 wt% tackifying resin, 20–30 wt% naphthenic or paraffinic oil, and 0.5–1.0 wt% antioxidant. Sigma-blade agitator speed of 30–60 rpm or twin-screw speed of 200–350 rpm is selected to disperse the styrene domains while keeping melt temperature below 185°C; temperature overshoot above this limit accelerates butadiene oxidation, visible as yellowing and an increase in melt viscosity. Adhesive components intended for food-packaging laminates are evaluated under 21 CFR 175.105 and 21 CFR 177.2600 for repeated food-contact rubber articles, while European obligation requires registration under REACH Regulation (EC) No 1907/2006, restriction screening under Annex XVII, and phthalate control under Directive 2005/84/EC. Melt flow rate is checked with ISO 1133-1:2022; production experience shows that viscosity drift greater than 10% after 4 h at processing temperature produces slot-die streaking and coat-weight variation in transfer coating. Terminal products are removable label stocks, high-shear carton-sealing tapes, nonwoven hygiene construction adhesives, and automotive interior lamination films. A common conversion fault is tackifier incompatibility: aliphatic-leaning resins separate from the butadiene midblock and migrate to the adhesive surface within 72 h, causing haze, tack loss, and loop-tack decline.
Footwear soling compounds containing Kraton™ D1493 P are formulated with 60–75 phr SBS, 30–40 phr process oil, 10–15 phr crystal polystyrene, 10–20 phr calcium carbonate, 0.3–0.5 phr hindered phenolic antioxidant, and 0.2–0.4 phr antiozonant when the sole edge is exposed to ozone in service. Melt compounding on a co-rotating twin-screw extruder with L/D 36–48 uses a barrel profile from 140°C at the feed throat to 175–190°C at the die, followed by underwater pelletizing after a 2.0–3.0 mm strand die. Injection molding of unit soles proceeds at melt temperature 165–185°C, injection pressure 60–80 MPa, mold temperature 25–40°C, and cooling time 20–35 s for sole thicknesses between 15–25 mm. For cellular soles, chemical blowing agent at 0.5–1.0 phr and cavity venting depth of 0.02–0.03 mm are required; residual moisture in the powder above 0.10 wt% produces silver streaking and weakens weld lines on production presses. European footwear compliance requires REACH Annex XVII phthalate restriction entries 51 and 52 and dimethyl fumarate restriction entry 22; mechanical acceptance references ASTM D412 tensile, ISO 34-1 tear, ISO 4649 abrasion, and SATRA TM174 flex cracking. Terminal products are injection-molded casual unit soles, direct-attached sandal soles, cellular midsole components, and die-cut insock sheeting. The principal injection-shop boundary is the narrow melt-temperature window: below 160°C the charge freezes in the nozzle, and above 190°C butadiene segment degradation causes surface marking and edge embrittlement after 72 h of ambient aging.
For modified bitumen waterproofing membranes, Kraton™ D1493 P is dispersed into oxidized or straight-run bitumen at 8–14 wt% using a high-torque paddle mixer at 170–185°C for 60–120 min until the compound passes a continuous polymer network check. The downstream calender line saturates polyester spunbond or glass-fiber mat with the SBS-bitumen compound at 8–20 m/min, applying 3.0–5.0 mm total thickness within ±0.2 mm cross-web tolerance. Low-temperature flexibility is evaluated with EN 1109 at -10°C to -20°C depending on membrane class, while dimensional stability after heating follows EN 1107-1. CE marking for roof waterproofing under EN 13707 and below-ground tanking under EN 13969 ties factory production control to notified body certification; fire performance is classified under EN 13501-5. Terminal products are torch-applied SBS-modified membranes, self-adhesive cold-applied rolls, bridge deck waterproofing sheets, and underlayments for standing-seam metal roofs. On production lines, web tension creep becomes an uncontrollable variable when compound temperature falls below 155°C, because the thickened melt cannot penetrate the carrier interstices and peel adhesion under ASTM D903 falls below the commonly specified 20 N/25 mm acceptance value.
Solventborne contact adhesives containing Kraton™ D1493 P are formulated at 8–15 wt% SBS dissolved in methyl ethyl ketone, acetone, and n-hexane or toluene at 25–35°C in a high-speed dissolver with 300–600 rpm agitator speed under nitrogen blanketing. Staged addition of the SBS powder and pre-slurrying in a static mixer are used to prevent gel bodies that form when local solvent wetting is incomplete or when the batch temperature exceeds 35°C. Explosive atmosphere classification for mixing and dosing equipment follows ATEX 2014/34/EU for Zone 1 or Zone 2 areas, and volatile organic compound limits are set under EU Directive 2004/42/EC for adhesives and sealants. Release testing includes solids content by ISO 3251 with tolerance of ±0.5 wt%, Brookfield viscosity at 25°C in the range of 2,000–6,000 mPa·s, and peel strength by ASTM D903; elastomer-to-substrate adhesion may also be checked by ASTM D413. Terminal products are contact adhesives for footwear sole attachment, furniture edge banding, insulation panel lamination, and construction sheet bonding. The main operational boundary is shear tolerance: entrained air from drum filling creates pinholes in spray-applied films, and solvent flash loss from open mixing vessels above 25°C shifts rheology beyond acceptable brushability within one operating shift.
Thermoplastic elastomer compounds based on Kraton™ D1493 P are produced with 30–50 wt% SBS, 30–50 wt% paraffinic or naphthenic oil, 10–20 wt% polypropylene as the thermoplastic phase, and 10–20 wt% mineral filler. A co-rotating twin-screw extruder with L/D 40–52 and segmented screw elements is operated at 180–210°C, screw speed 250–450 rpm, and specific energy input of 0.20–0.35 kWh/kg; polypropylene is introduced upstream while the SBS/oil dry blend is fed after the first kneading block to limit shear heating. Underwater pelletizing at die-face temperature 190–205°C and water temperature 20–30°C produces dense spherical pellets for injection molding or profile extrusion. Electrical and electronic component compliance uses RoHS Directive 2011/65/EU, consumer goods PAH screening follows AfPS GS 2019:01 PAK where applicable, and European product obligations include REACH Regulation (EC) No 1907/2006. Hardness is measured with ISO 48-4 Shore A, tensile strength with ISO 37, compression set after 22 h at 70°C under ISO 815-1, and oil bleeding gravimetrically after 72 h at 70°C; typical soft-touch targets are Shore A 45–65, tensile strength 4–8 MPa, and compression set below 45%. Terminal products are overmolded soft-touch grips for power tools, automotive floor mats, anti-fatigue matting, and equipment edge-protection extrudates. A recognized compounding failure is oil phase inversion at paraffinic oil loadings above 50 wt%: the compound may still extrude but exudes oil on storage and develops compression set above 60%, especially when pelletizing water temperature exceeds 40°C and pellet fusion occurs.
| Application | Standard or regulation | Test method or clause | Typical acceptance target |
|---|---|---|---|
| Road polymer-modified bitumen | EN 14023:2010 | EN 13398 | Elastic recovery ≥ 70% at 25°C |
| Road polymer-modified bitumen | ASTM D5976 | ASTM D36 | Softening point per project PG requirement |
| Hot-melt adhesive | 21 CFR 175.105 | FDA component migration | Food-packaging adhesive component compliance |
| Hot-melt adhesive | ISO 1133-1:2022 | Melt flow rate | Process-defined MFR window |
| Footwear soling | REACH Annex XVII | Entries 51, 52, 22 | Phthalates < 0.1 wt%, DMF restricted |
| Waterproofing membrane | EN 13707 | EN 1109 | No cracking at -10°C or specified class temperature |
| Solventborne adhesive | EU Directive 2004/42/EC | VOC content | Category-specific ready-for-use limit |
| TPE compound | RoHS Directive 2011/65/EU | Restricted substance screening | Pb, Cd, Hg, Cr(VI), PBB, PBDE limits |
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Kraton™ D1493 P is a linear styrene-butadiene-styrene block copolymer supplied as a low-dust porous pellet. In this product the terminal polystyrene blocks are covalently attached to an unsaturated polybutadiene midblock rather than to a hydrogenated ethylene-butylene midblock, which distinguishes the material from SEBS grades such as Kraton G1651. Supplier documentation defines the grade as a high-styrene linear SBS with nominal bound styrene content of 38 wt%; the butadiene segment retains olefinic unsaturation that permits sulfur or peroxide crosslinking but also imposes tighter thermal-oxidative processing limits. The solid-state properties arise from microphase separation of polystyrene domains. Heating above the order-disorder transition reduces melt viscosity, making the material reprocessable by extrusion, injection molding, and hot-melt coating.
The practical consequence of the 38 wt% bound styrene architecture is that D1493 P occupies a high-modulus position within the unsaturated SBS product range. Compounds based on D1493 P exhibit higher Shore A hardness as measured by ASTM D2240-15e1, higher tensile modulus at 300% elongation as measured by ASTM D412-16, and higher heat resistance than compounds based on Kraton D1101 or D1102. The same styrene content reduces low-temperature flexibility and increases sensitivity to aromatic process oils. Formulators therefore select this grade when ambient or elevated temperature load-bearing properties dominate over low-temperature impact or softness.
For linear SBS, the two main structural variables are the polystyrene block fraction and the diblock content. A higher polystyrene block fraction increases the volume fraction of hard domains and raises the plateau modulus at service temperatures between the polybutadiene glass transition and the polystyrene glass transition. The low diblock content in D1493 P ensures that most chains terminate in polystyrene blocks that participate in the network. Free diblock chains, by contrast, act as network defects because one end cannot anchor in a styrene domain. Comparative data for Kraton D1101, Kraton D1155, and Kraton D1493 P are summarized in Table 1. The values are representative of current supplier technical bulletins; lot-specific certificates of analysis control batch acceptance.
| Property | Test method | Kraton D1101 | Kraton D1155 | Kraton D1493 P |
|---|---|---|---|---|
| Bound styrene | Supplier FAM/FTIR | 31 wt% | 40 wt% | 38 wt% |
| Tensile strength at break | ASTM D412-16 | 31 MPa | 32 MPa | 30 MPa |
| Elongation at break | ASTM D412-16 | 880% | 700% | 700% |
| Hardness Shore A | ASTM D2240-15e1 | 71 | 87 | 87 |
| Specific gravity | ASTM D792-20 | 0.94 | 0.96 | 0.96 |
| Melt flow rate at 200 °C / 5 kg | ISO 1133-1:2022 | <1 g/10 min | 3 g/10 min | 20 g/10 min |
The higher melt flow rate of D1493 P relative to D1155 is significant for compounding. It permits lower melt pressure at typical die temperatures while retaining high Shore A hardness. The practical effect is that D1493 P can be used at higher throughput on a given compounding line, provided the shear-heating limits in the next section are respected.
On a co-rotating twin-screw extruder with 40:1 L/D and segmented screw elements, the barrel set points from zone 2 to zone 8 should be maintained at 150–190 °C. The feed throat must remain below 50 °C to prevent pellet bridging and premature softening. Melt temperature measured at the die plate with an immersion thermocouple should not exceed 210 °C; excursions beyond 220 °C for more than 2 min initiate crosslinking across the unsaturated polybutadiene midblock. The onset is observed as a progressive rise in die pressure, gel specks in the extrudate, and a shift in the butadiene unsaturation infrared absorption. A gear pump or static mixer upstream of the die is recommended to reduce melt-temperature variation to ±3 °C. Pre-drying at 70–80 °C for 2 h in a desiccant dryer is required when pellet surface moisture exceeds 0.1 wt%; moisture is not hydrolytically destructive to the SBS backbone but produces surface splay and bubbles.
When changing from halogenated polymers or filled PVC compounds, purging with a styrene-based purging compound or fractional melt high-density polyethylene is required. Residual halogenated material drives acid-catalyzed cleavage of the polybutadiene segment and must not be allowed to remain in the screw channels, barrel vents, or die manifold. Direct contact with copper alloys should be avoided because copper ions accelerate autoxidation of the unsaturated midblock.
Injection molding of D1493 P is conducted with nozzle temperatures of 190–200 °C, mold temperatures of 20–40 °C, and injection pressures of 50–100 MPa depending on part wall thickness and gate geometry. Because the material is a thermoplastic elastomer, holding pressure and screw cushion are set lower than for semi-crystalline engineering resins; the low melt viscosity can produce flash if clamp force is insufficient. Mold release is normally not required, but external release agents should be avoided when post-mold printing or adhesion is planned.
In oil-extended compounds, the aromatic selectivity of the styrene phase governs plasticizer distribution. D1493 P accepts paraffinic or naphthenic oil up to 50 phr while retaining a Shore A hardness above 30; above 50 phr, tensile strength and tear resistance fall when measured by ASTM D412-16 and ASTM D624-00(2020). Aromatic oils plasticize the styrene domains and should be minimized unless a specific reduction in hardness is required. The acceptable processing oil level is determined by measuring the compound’s Shore A hardness after 7 days at 23 °C and 50% relative humidity to detect time-dependent oil bleed.
Hot-melt pressure-sensitive adhesive formulations based on D1493 P typically combine the polymer with hydrogenated hydrocarbon tackifier and process oil. At oil loadings above 50 phr, the aliphatic oil fraction selectively swells the polybutadiene midblock. The resulting softening of the rubbery matrix reduces die-cutting shear holding power despite high styrene content. Loop tack measured by ASTM D6195-03(2019) and 180° peel adhesion measured by ASTM D6862-11 are highly sensitive to the ratio of aromatic end-block resin to aliphatic oil. A reinforcing aromatic end-block resin added at 5–15 phr restores the polystyrene domain glass transition and preserves shear adhesion failure temperature. In the absence of an end-block resin, formulators should keep total oil plus liquid tackifier below 70 phr and verify hot melt viscosity at 180 °C with a Brookfield RVT viscometer at 20 rpm.
For solvent-borne pressure-sensitive adhesives, D1493 P is dissolved in toluene, cyclohexane, or ethyl acetate/toluene blends at solids of 25–40 wt%. The low diblock content increases solution viscosity relative to low-styrene grades at equal solids, as measured by Brookfield rotational viscometry at 25 °C and 20 rpm. Coating by knife-over-roll or slot die is performed with solution temperature maintained at 20–25 °C; higher temperature reduces viscosity but accelerates solvent evaporation and can cause surface skinning. The dried film is non-tacky at low adhesive coat weight if end-block content is not plasticized, which can be advantageous for heat-activated bonding.
In polymer-modified bitumen, D1493 P is dispersed at 170–190 °C with a high-shear rotor-stator mill. The high styrene content raises the viscosity and elastic recovery of the modified binder at lower addition levels than D1101. Rotational viscosity at 135 °C measured by EN 13302 and softening point by EN 1427 are the primary controls. Production-scale polymer-modified bitumen plants commonly use high-shear processing to achieve a stable droplet morphology within 60–90 min when the base bitumen is a 70/100 pen grade; low-shear storage stability is then evaluated by the tube test under EN 13399.
Regulatory compliance positions require confirmation from the current supplier declaration. The following matrix lists the applicable frameworks for unsaturated SBS grades; it is not a substitute for food-contact or medical-grade certification.
| Regulatory area | Designation | Applicability statement |
|---|---|---|
| U.S. food-contact | 21 CFR 177.1810 | Styrene block copolymers may be used as components of articles intended for food contact subject to end-use limitations and migration testing specified in the regulation. |
| EU polymer registration | REACH 1907/2006/EC | Polymer registration/exemption status and SVHC declarations are provided by the current supplier safety data sheet. |
| Restriction of hazardous substances | RoHS 2011/65/EU | The product is not expected to contain restricted substances above the limits in Annex II when processed without contaminated regrind. |
| Polymer-modified bitumen | EN 14023 | Compliance is determined on the final modified binder, not on the neat polymer alone. |
Storage stability is controlled by the phenolic antioxidant system incorporated during manufacture. Pellets should be kept below 30 °C and relative humidity below 50% in sealed original packaging. Under these conditions, the product can be stored for at least 24 months without measurable increase in gel content as determined by filtration of a toluene solution. Re-wetting of pellets before processing does not hydrolyze the polymer, but requires re-drying to avoid surface defects. The unsaturated midblock remains sensitive to prolonged UV exposure; outdoor applications require carbon black or a UV-stabilized compound.