| HS Code | 153967 |
| Chemical Family | Styrene-butadiene-styrene block copolymer (SBS) |
| Polymer Structure | Linear |
| Styrene Content | 31 % |
| Butadiene Content | 69 % |
| Density | 0.94 g/cm³ |
| Melt Flow Index | 1.0 g/10 min |
| Shore A Hardness | 65 |
| Tensile Strength | 250 kg/cm² |
| Elongation At Break | 700 % |
| Solution Viscosity | 1,500 mPa·s at 25% in toluene |
| Volatile Matter | 0.5 % max |
| Ash Content | 0.2 % max |
As an accredited Kumho Petrochemical KTR® SBS 655 factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Kumho Petrochemical KTR® SBS 655 is supplied in 25 kg moisture-resistant paper bags, palletized for industrial handling and storage. |
| Container Loading (20′ FCL) | A 20-foot FCL container is securely loaded with Kumho Petrochemical KTR® SBS 655 for safe ocean transport. |
| Shipping | Kumho Petrochemical KTR® SBS 655 is shipped as solid styrene-butadiene-styrene block copolymer pellets in moisture-resistant bags or boxes. It is not classified as dangerous goods for DOT, IMDG, IATA, or ADR transport. Keep dry, cool, and away from direct sunlight and ignition sources. |
| Storage | Store Kumho Petrochemical KTR® SBS 655 in a cool, dry, well-ventilated area away from direct sunlight, heat, ignition sources, moisture, and strong oxidizers. Keep original containers closed and palletized to prevent deformation or contamination. Avoid prolonged exposure to UV light and ozone. Maintain stable, moderate temperatures and follow the manufacturer’s SDS and local regulations. |
| Shelf Life | Kumho Petrochemical KTR® SBS 655 typically has a 12-month shelf life when stored dry in original sealed packaging, away from heat and sunlight. |
In paving-grade polymer-modified bitumen (PMB) production, KTR® SBS 655 is introduced into straight-run bitumen preheated to 160–180 °C at a dosage of 3.0–7.5 wt% before high-shear dispersion. The linear SBS triblock architecture governs the modification mechanism: polystyrene end-blocks phase-separate into glassy domains with a service temperature below their glass transition, while the polybutadiene midblock forms a continuous elastomeric network that absorbs thermal and mechanical strain. Without sufficient shear, the initial pellet or crumb morphology persists as coarse agglomerates exceeding 50 μm, and the resulting PMB can fail hot storage stability within 72 h. A rotor-stator high-shear mill or Siefer colloidal mill operating at 3,000–5,000 rpm is used until the dispersed SBS particle size falls below 10–20 μm, after which low-shear agitation continues for 60–120 min to permit progressive swelling of the rubber-rich phase. Barrel and mixing head jacket temperatures are controlled at 175–190 °C; sustained exposure above 200 °C for more than 2 h accelerates oxidative scission of the polybutadiene midblock and can reduce elastic recovery by up to 15 percentage points in laboratory ageing trials.
| SBS content (wt%) | Ring-and-ball softening point (°C, ASTM D36/D36M) | Elastic recovery at 25 °C (%, ASTM D6084/D6084M-21) | Penetration at 25 °C (dmm, ASTM D5/D5M-20) |
|---|---|---|---|
| 3.0 | 58–65 | 45–60 | 50–60 |
| 4.5 | 68–75 | 60–75 | 45–55 |
| 6.0 | 78–85 | 75–90 | 40–48 |
| 7.5 | 85–92 | 85–95 | 35–42 |
Routine PMB evaluation follows EN 14023:2010 and ASTM D5976-22 for selection of base materials and verification of final properties. Ring-and-ball softening point according to ASTM D36/D36M typically rises from 48–52 °C for the unmodified 70/100 penetration-grade bitumen to 78–85 °C at 6.0 wt% SBS. Elastic recovery at 25 °C measured by ASTM D6084/D6084M-21 commonly exceeds 80% when the SBS network is fully dispersed; values below 60% indicate incomplete phase inversion. Penetration at 25 °C by ASTM D5/D5M-20 decreases from 65–75 dmm to 35–45 dmm depending on SBS loading, and Fraass breaking point by EN 12593 can shift to −18 °C or lower with a suitable low-wax flux. Storage stability is evaluated in a vertical aluminium tube at 180 °C for 72 h under EN 13399; the difference in softening point between top and bottom sections should remain below 5 °C. Published data for KTR® SBS 655 specifically in high-modulus 7.5 wt% PMB with polymer-modified microsurfacing is limited; pilot-mill validation is recommended because equipment shear history, base bitumen asphaltene content, and additive sulphur crosslinking alter the final storage modulus.
Low-temperature flexibility in SBS-modified bituminous roofing membranes is governed by the continuity of the styrene-rich physical crosslink network and by the plasticiser partition between bitumen and rubber phase. In calender-grade formulations, KTR® SBS 655 is used at 8–14 wt% together with 55–65 wt% oxidised or distilled bitumen, 20–25 wt% mineral filler such as talc or calcium carbonate, and 1–3 wt% antioxidant. The mixing sequence is performed in a heated double-sigma blade mixer at 180–190 °C; the SBS is added after the bitumen and filler have reached a homogeneous viscosity, then shear is maintained at 40–70 rpm until a uniform leather-like compound is obtained. Calendering onto a polyester or glass-fibre carrier at 0.8–1.5 m/min line speed produces a 3–5 mm thick membrane, and the finished sheet is cooled through the glass transition of the polystyrene domains at 15–40 °C before rolling.
Performance is tested under EN 13707:2013 for reinforced bitumen sheets for roofing. Cold bending at −20 °C using EN 1109 requires no visible cracking; formulations with high filler loading above 25 wt% may fail this criterion because filler particles create stress concentration points that nucleate fracture through the polybutadiene midblock. Dimensional stability at 80 °C for 6 h must remain within ±0.5%, and tensile strength per ASTM D5147/D5147M-18 is typically 4.0–6.0 MPa in the machine direction. For exposed roofing membranes, external fire performance is classified under EN 13501-5 with mineral granules, and formulations must be adjusted so that the asphalt-rich surface layer retains sufficient cohesion to anchor the granules without being displaced during the heat of combustion. Addition of paraffinic process oils must be limited to 5 wt% or less; above this limit the oil migrates into the styrene domains over time, lowers the effective glass transition, and reduces the upper service temperature before indentation failure occurs.
Injection-grade midsole compounds containing KTR® SBS 655 are typically compounded on a corotating twin-screw extruder with an L/D ratio of 40:1 and screw speed 250–400 rpm. The formulation contains 100 phr SBS, 20–40 phr general-purpose polystyrene, 5–20 phr naphthenic or paraffinic processing oil, 0.5–1.5 phr azodicarbonamide blowing agent, and 0.1–0.4 phr dicumyl peroxide crosslinking agent. Barrel temperature zones are set between 145 °C and 175 °C; the melt temperature at the die must remain below 190 °C to prevent premature decomposition of the blowing agent and to limit thermal gelation in the polybutadiene segments. The resulting pellets are injection moulded into microcellular sole units at clamp pressures of 80–120 t depending on cavity area, with mould temperature held at 30–50 °C and back pressure 5–10 bar during plastication to avoid gas phase segregation. Finished microcellular parts reach a density of 0.30–0.45 g/cm³, Shore A hardness 55–70, tensile strength per ASTM D412-16 of 8–12 MPa, elongation 500–700%, and compression set after 24 h at 70 °C of 20–35% according to ASTM D395-18 Method B.
Process conflicts arise when the compound is blended with high-cis polybutadiene rubber above 20 phr; the difference in solubility parameter creates macroscopic phase separation at the skin of the moulded part, visible as surface haze and tear strength loss. High melt temperatures above 200 °C during injection moulding create gas blister defects at the part surface because the blowing gas nucleates inhomogeneously at degraded rubber domains. Oil selection is critical: aromatic content above 5 wt% in the extrusion formula softens the styrene-rich phase and reduces dimensional stability of the expanded sole after 48 h annealing at 50 °C. Published data for KTR® SBS 655 in microcellular injection foam is limited to standard formulations; rheological characterisation by capillary rheometry at 180 °C is required before transfer to high-pressure foam lines.
Hot-melt pressure-sensitive adhesives based on KTR® SBS 655 are formulated with 20–40 wt% hydrogenated hydrocarbon tackifier, 5–15 wt% naphthenic oil, and 0.5–1.5 wt% stabiliser. Mixing is carried out under a nitrogen blanket in a horizontal sigma-blade mixer at 160–180 °C until the tackifier is fully dissolved and the viscosity stabilises. For slot-die coating at 120–180 °C, the melt viscosity should be held between 5,000 mPa·s and 25,000 mPa·s at 180 °C; below 5,000 mPa·s the coating weight varies beyond ±2 g/m², and above 25,000 mPa·s the die pressure rises above 40 bar and generates transverse streak defects. The C5/C9 resin choice must be matched to the polybutadiene midblock; high softening point resins above 115 °C reduce tack but raise the shear adhesion failure temperature to 70–85 °C.
Pressure-sensitive performance is measured by FINAT FTM 1 loop tack and ASTM D1876 180° peel on stainless steel; typical values are 8–14 N/25 mm loop tack and 6–10 N/25 mm peel depending on coating thickness of 25–35 μm. Shear resistance under FINAT FTM 8 at 40 °C with a 1 kg load often exceeds 24 h. At tackifier loadings above 45 wt%, the rubbery plateau shortens and the adhesive loses cohesive strength, leading to adhesive transfer and ghost marks on release liner. Ageing at 70 °C for 7 days in a forced-air oven may reduce peel by up to 15% unless the unsaturated midblock is adequately stabilised. The suitability window is narrower than for low-diblock SIS grades if the certificate of analysis confirms higher diblock content; use at −25 °C requires validation by low-temperature peel and mandrel flex tests before specifying KTR® SBS 655 for freezer-grade label stock.
Melt blending of KTR® SBS 655 with general-purpose polystyrene (GPPS) is performed on a co-rotating twin-screw extruder at 190–210 °C with an L/D ratio of 36:1 or larger. Addition of 10–30 wt% SBS creates a two-phase morphology in which the polybutadiene midblock forms discrete rubber particles with diameters of 0.5–2.0 μm, while the polystyrene end-blocks and GPPS matrix form a continuous rigid phase. The resulting high-impact sheet exhibits notched Izod impact strength of 8–15 kJ/m² according to ISO 180, compared with 1.5–2.5 kJ/m² for unmodified GPPS. Tensile strength per ISO 527-2:2021 decreases from 45 MPa for GPPS to 28–35 MPa at 30 wt% SBS, and flexural modulus per ISO 178 falls from 3.0 GPa to 1.5–1.8 GPa. Melt mass-flow rate according to ISO 1133-1:2022 at 200 °C under 5 kg drops by 30–60% relative to unmodified GPPS, depending on the SBS loading and screw shear history.
Thermo-oxidative degradation of the polybutadiene midblock is the main process risk: when melt temperatures exceed 220 °C or residence time exceeds 3 min, gel particles form and progressively blind screen packs of 80 mesh or finer. Processors should meter SBS pellets downstream of the first feed zone to limit thermal history and use a vacuum devolatilisation port at −0.08 MPa to remove moisture and low-molecular-weight volatiles. The blend should be purged with GPPS after run completion; shutdown without purging leaves SBS-rich residue that degrades on restart and causes black specks in the next production cycle. For thin-gauge sheet below 1 mm, chill-roll temperature should be held at 60–80 °C to minimise frozen-in orientation and to prevent the sheet from cracking during die cutting.
Extruded anti-fatigue mats and structural vibration-damping sheets use KTR® SBS 655 as the base elastomer because its styrenic physical crosslinks provide recoverable energy dissipation under cyclic compression. A typical compound contains 100 phr SBS, 30–50 phr calcium carbonate or barium sulphate, 10–20 phr paraffinic oil, and 1–2 phr antioxidant, processed on a single-screw extruder with a flat die at 165–185 °C. The extrudate is calendered and embossed to produce a sheet thickness of 2–8 mm; dynamic mechanical analysis under ISO 6721-1:2019 at 25 °C and 10 Hz yields a loss factor tan δ of 0.25–0.45. Tensile set after 100% elongation is 15–25% according to ISO 2285, indicating recovery from short-term deformation but insufficient creep resistance for sustained compressive loads above 0.05 MPa at temperatures above 50 °C. Shore A hardness of the filled sheet is typically 60–75. When barium sulphate is used at 50 phr to increase density for acoustic damping, the increase in compound viscosity raises melt temperature by 5–10 °C and reduces line speed by 10–20%; screw cooling is required to avoid scorch. Published data for KTR® SBS 655 in high-frequency acoustic damping above 500 Hz is limited; material selection should be confirmed by DMA master curve generation over the target temperature and frequency range.
| Application segment | Primary performance standard | Test characteristic | Regulatory reference |
|---|---|---|---|
| PMB paving | EN 14023:2010, ASTM D5976-22 | softening point, elastic recovery, storage stability | EU Construction Products Regulation, REACH |
| Roofing membrane | EN 13707:2013, ASTM D5147-18 | cold bending, tensile, dimensional stability | EN 13501-5, RoHS 2011/65/EU |
| Footwear | ASTM D412-16, ASTM D395-18 | tensile strength, compression set | REACH SVHC screening |
| HMPSA | FINAT FTM 1, ASTM D1876 | loop tack, 180° peel, SAFT | FDA 21 CFR 175.105 if indirect food contact |
| GPPS blend | ISO 180, ISO 527-2:2021 | Izod impact, tensile modulus | REACH, RoHS |
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Kumho Petrochemical KTR® SBS 655 is a linear styrene-butadiene-styrene block copolymer supplied as a porous crumb. The material has polystyrene end blocks and a polybutadiene midblock; thermodynamic incompatibility between the two segment types produces a physically crosslinked morphology at ambient temperature. The grade is positioned in the 65 Shore A hardness class. Processing involves reversible thermal dissociation of styrene-rich domains, while the unsaturated midblock remains sensitive to oxidative chain scission when melt residence time is prolonged. KTR 655 is specified where controlled melt viscosity, low-temperature flexibility, and elastic recovery are required in injection-moulded footwear, solvent-borne adhesives, and asphalt modification. The sections that follow address lot-release parameters, process boundaries, and differences from other products in the KTR SBS range.
Hardness is not an independent variable in SBS design; it follows from bound styrene content and the volume fraction of glassy polystyrene domains. For KTR 655, bound styrene content is controlled within 32 ± 1 wt% when evaluated by solvent-extraction or infrared methods aligned to ISO 21561. At this styrene level, compression-moulded sheets conditioned according to ASTM D618-13 and tested under ASTM D2240-15 typically exhibit Type A durometer readings of 63–67. Tensile properties determined on 2 mm plaques under ASTM D638-14 usually show tensile strength of 12–14 MPa, elongation at break of 550–700%, and a 300% modulus of 1.5–2.5 MPa. These values are representative product-class ranges and are not a substitute for a certificate of analysis.
The hardness target provides a practical balance in thin-wall injection moulding because the elastomer retains a higher midblock loss tangent than a 75–80 Shore A grade at the polybutadiene glass transition near -90 °C. In comparison with KTR 101 and KTR 201, which occupy higher hardness classes, KTR 655 exhibits more pronounced Mullins stress softening under cyclic deformation. When fatigue testing is performed on a Bally flexometer after 100 000 cycles, crack-initiation resistance is governed by styrene-domain continuity. Published data for this specific configuration is limited, so qualification should include flex-cut resistance using ISO 4643 or SATRA TM60 rather than relying solely on Shore A measurement.
Solvent-borne pressure-sensitive adhesive formulations prepared with KTR 655 are typically dissolved at 30–40 wt% solids in toluene, cyclohexane/acetone blends, or toluene/ethyl acetate mixtures. The linear structure of KTR 655 yields lower Brookfield solution viscosity than high-molecular-weight radial SBS grades at equivalent solids content. A 30 wt% solution in toluene at 25 °C may show viscosity in the range of 5–15 Pa·s when measured with a Brookfield RVT spindle No. 4 at 20 rpm; actual viscosity is batch-dependent. In adhesive coating, the crumb must be pre-dried at 60–70 °C for 1–2 h if ambient relative humidity exceeds 60%, because moisture trapped in the crumb can produce microvoids in the cast film and reduce tack.
Adhesives containing KTR 655 should be stabilised with a synergistic phenolic/phosphite antioxidant system. The polybutadiene midblock requires oxidative protection, and addition of 0.2–0.5 phr of a hindered phenolic plus 0.1–0.2 phr of a phosphite secondary stabiliser is common. Primary amine-based additives should be avoided; under molten conditions, residual amine species can accelerate oxidative gel formation in the unsaturated midblock, and the resulting increase in complex viscosity can clog slot-die coating heads. This incompatibility is not captured by tensile testing under ASTM D638-14 and must be evaluated by torque rheometry at 180 °C.
Compounding KTR 655 on a co-rotating twin-screw extruder with an L/D ratio of 40:1 requires barrel setpoints of 170–190 °C, with die temperature near 190 °C. A screw profile using distributive mixing elements and low-pressure kneading blocks is preferred, because aggressive dispersive blocks generate local melt temperatures above 210 °C. Above 210 °C, the polybutadiene midblock can undergo simultaneous free-radical chain scission and crosslinking, producing gel particles that appear as surface defects in injected parts. Vacuum venting at -0.08 MPa is applied after the melting zone to strip residual volatiles; if vent flow becomes unstable, specific mechanical energy input should be reduced by increasing feed-zone temperature or reducing screw speed. In production-scale runs, batch-to-batch variation in melt flow index is normally controlled at ±1.5 g/10 min under ISO 1133-1:2022 at 190 °C and 5 kg load. Torque fluctuations greater than 5% of the mean value during continuous extrusion indicate local oxidation or feed inconsistency.
A pre-compounded masterbatch with 0.3 phr of phenolic antioxidant and 0.1 phr of phosphite stabiliser is sufficient for most closed-mixing operations. Zinc stearate at 0.5 phr can improve roll-release, but it may slightly delay styrene-domain reformation after cooling and should not exceed 1 phr. When the stabiliser package is fully consumed, the first measurable change is usually an increase in gel content rather than a change in melt flow index. This operational boundary is expressed as melt residence time at 190 °C; production trials should not exceed 90 s from feed throat to die without dedicated antioxidant supplementation.
Formal qualification of KTR 655 should use the supplier certificate of analysis. Representative control ranges and associated standards are shown below for the product class, but production lots may differ within the supplier specification.
| Parameter | Test method | Representative control range |
|---|---|---|
| Bound styrene content | ISO 21561 | 32 ± 1 wt% |
| Specific gravity | ASTM D792-20 | 0.94 ± 0.01 |
| Hardness, Type A | ASTM D2240-15 | 63–67 |
| Tensile strength at break | ASTM D638-14 | 12–14 MPa |
| Elongation at break | ASTM D638-14 | 550–700% |
| Tensile modulus at 300% | ASTM D638-14 | 1.5–2.5 MPa |
| Melt flow index, 190 °C/5 kg | ISO 1133-1:2022 | 3–7 g/10 min |
| Volatile matter | ASTM D5668-21 | ≤0.5 wt% |
| Ash content | ASTM D5667-21 | ≤0.5 wt% |
Differences from KTR 401 and KTR 501 are primarily rheological and compositional. KTR 401 is oil-extended; its flow is modified by hydrocarbon oil, and migration of that oil can occur in heat-ageing or contact applications. KTR 655 is non-oil-extended, which avoids plasticiser migration under sustained heat. Compared with KTR 201, KTR 655 has a lower Shore A hardness and a narrower styrene-domain order-disorder transition. This shortens cycle time in thin-wall injection moulding but reduces shear resistance in thick sections.
| Attribute | KTR 101 | KTR 201 | KTR 401 | KTR 655 |
|---|---|---|---|---|
| Hardness range, Type A | 75–80 | 68–72 | 45–55 | 63–67 |
| Oil extension | No | No | Yes | No |
| Melt flow index, 190 °C/5 kg | 0.3–0.8 g/10 min | 1–3 g/10 min | 5–15 g/10 min | 3–7 g/10 min |
| Typical use | High-wear soles | General footwear | Soft compounds | Thin-wall outsoles, adhesives, asphalt |
Thin-wall injection moulding of KTR 655 compounds is performed on hydraulic or electric machines with a clamping force of 800–1 500 kN for multi-cavity footwear outsoles. Melt temperature at the nozzle should be 180–200 °C; higher settings accelerate the transition from physical to oxidative crosslinking. Mould temperature is typically 30–50 °C, and cooling time is governed by styrene-domain reformation rather than simple enthalpy removal. Ejector marks may appear if the part is demoulded before the surface temperature falls below 60 °C. In production, a nucleated or fast-crystallising SEBS alternative is unnecessary unless ozone resistance is required, because KTR 655 contains an unsaturated midblock and must be protected with a phenolic antioxidant plus a UV absorber for outdoor applications. Ozone resistance is tested under ASTM D1149 or ISO 1431-1.
In polymer-modified bitumen, KTR 655 is incorporated at 4–6 wt% based on bitumen mass. A high-shear mill with a rotor-stator head at 5 000–6 000 rpm is used at 180–190 °C for 2–4 h. During digestion, the SBS phase swells with maltenes, and phase inversion occurs when the SBS-rich phase becomes continuous. If the blend is stored below 170 °C, the density difference between the SBS-rich and asphaltene-rich phases increases and separation can occur. Storage stability should be tested under EN 13399, while low-temperature ductility and elastic recovery are evaluated according to EN 13587 and EN 13398. Typical elastic recovery above 70% after elongation to 200 mm is observed in suitable base bitumens; exact values vary with bitumen composition.
The SBS particle size after dispersion should remain below 10 µm. If particles exceed 20 µm, lower-temperature ductility is impaired. On production-scale silo storage, a gentle mixer or recirculation loop operating at 175–185 °C prevents skin formation. Moisture ingress must be excluded because steam expansion during hot-mix addition creates pinholes in the binder film. When comparing KTR 655 with radial SBS grades, the linear structure may produce lower high-temperature viscosity but comparable low-temperature crack resistance in the same base bitumen; however, published data for this specific configuration is limited and must be confirmed by EN 14023 testing of the final polymer-modified binder.
Flame-retardant compounds containing KTR 655 require careful selection of halogenated additives. Brominated flame retardants operating above 200 °C can release acidic species that attack the unsaturation and cause premature gel formation. Antimony trioxide at 3–5 phr and alumina trihydrate at 20–40 phr can be used if the compound is processed below 190 °C. Formaldehyde-releasing or amine-catalytic systems often used in flexible polyurethane are not compatible; they accelerate oxidation of the polybutadiene midblock. These exclusions can be detected by torque-rheometer tests at 180 °C with a 30 min residence time.