| HS Code | 827498 |
| Productname | Kraton™ G SEBS-Comp. G2708 GU-N |
| Manufacturer | Kraton Corporation |
| Polymertype | SEBS compound |
| Form | Pellets |
| Color | Natural |
| Density | 0.90 g/cm³ (typical) |
| Shoreahardness | 70 (typical) |
| Tensilestrength | 4.0 MPa (typical) |
| Elongationatbreak | 500% (typical) |
| Meltflowrate | 8–15 g/10 min at 230°C/2.16 kg (typical) |
| Compressionset | 25–30% at 23°C/72 h (typical) |
| Processingmethod | Injection molding and extrusion |
As an accredited Kraton Kraton™G SEBS-Comp. G2708 GU-N factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Kraton™ G SEBS-Comp. G2708 GU-N is packaged in palletized 25 kg moisture-resistant bags as free-flowing pellets. |
| Container Loading (20′ FCL) | Kraton™G SEBS-Comp. G2708 GU-N in standard export packaging, palletized and secured, loaded into a 20′ FCL for sea freight. |
| Shipping | Kraton™ G SEBS-Comp. G2708 GU-N is a non-hazardous thermoplastic elastomer compound and is not regulated for transport (no UN number, hazard class, or packing group). Ship in clean, dry, sealed packaging or containers at ambient temperature, protected from moisture, contamination, direct sunlight, and excessive heat. Use standard industrial handling. |
| Storage | Store Kraton™G SEBS-Comp. G2708 GU-N in a cool, dry, well-ventilated area away from direct sunlight, heat, flames, and strong oxidizers. Keep containers tightly closed, use original packaging, and prevent contamination or moisture pickup. Avoid prolonged high-temperature exposure and inspect containers regularly. Maintain good housekeeping and follow the SDS plus local regulations for specific storage requirements. |
| Shelf Life | Kraton G2708 GU-N typically has a 24-month shelf life from manufacture when stored unopened in original packaging under dry, cool conditions. |
Medical device processors running multi-layer co-extrusion lines with single-screw extruders in the 24:1 to 30:1 L/D range have evaluated Kraton™ G2708 GU-N as the styrenic block copolymer layer in fluid transport assemblies where post-autoclave clarity and low extractables are part of the validation file. In this configuration the compound is blended with polypropylene homopolymer at 60–80 wt% SEBS compound to 20–40 wt% PP homopolymer; a processing stabiliser package of 0.05–0.15 wt% hindered phenolic antioxidant is added under nitrogen-blanketed twin-screw compounding at 200–230°C. Compliance evidence typically includes FDA 21 CFR 177.1810 for styrenic block copolymers in repeat-use rubber articles, USP Class VI acute systemic injection and intracutaneous reactivity data, ISO 10993-5:2009 cytotoxicity evaluation, and sterilisation validation under ISO 11135:2014 ethylene oxide or ISO 17665-1:2006 steam. The downstream production process is usually a two-stage operation: first, melt filtration through a 100–150 mesh screen pack to remove gel particles above 80–120 µm; second, extrusion of tubing with wall thickness 0.6–1.2 mm at melt temperature 180–210°C. Post-extrusion annealing at 80–100°C for 30 min is used to reduce frozen-in orientation that otherwise induces kinking at bend radii below 2× outer diameter. Terminal finished product types include pressure monitoring tubing, peristaltic pump segments for dialysis equipment, syringe plunger tips, and drip chamber seals.
Because peel strength between a soft TPE-S and PC/ABS depends on interfacial temperature rather than barrel settings, trials on vertical rotary injection moulding machines with clamp force between 800 kN and 1,600 kN have used Kraton™ G2708 GU-N as the soft-segment component in a TPE-S formulation at 30–50 wt% SEBS compound, 10–20 wt% polypropylene, 20–40 wt% white mineral oil, and 0–10 wt% functionalised SEBS or polybutene-1 as a flow and tie modifier. The processing window requires pre-drying at 70°C for 2 h when ambient relative humidity exceeds 60%, because residual moisture leads to surface splay and weakens the bond line to PC/ABS below 2.5 N/mm peel strength. Amine-based antistatic additives above 0.2 phr should be avoided because they migrate to the interface during environmental cycling and lower peel strength. Barrel temperatures are maintained at 200–230°C, the substrate is heated to 100–140°C at the interface before the second shot, and holding pressure is held at 30–50 MPa for 5–10 s. Compliance is normally demonstrated with REACH Article 33 SVHC disclosure, RoHS 2011/65/EU Annex II restricted substance screening, and flow characterisation under ISO 1133-1:2022; adhesion evaluation is performed by ISO 527-1:2019 tensile testing of overmoulded plaques and by environmental cycling at 85°C/85% RH for 168 h. Terminal finished product types include power-tool soft grips, handheld consumer electronics overmoulds, toothbrush handles, and hand-tool cushions.
In homopolymer polypropylene compounding on a co-rotating twin-screw extruder with an L/D of 40:1, the incorporation of Kraton™ G2708 GU-N at 5–15 wt% lowers the ductile-brittle transition temperature without dropping melt flow below the specification floor. The compound is introduced via a side feeder after the PP melt has reached 200°C; screw speed is maintained at 400–600 rpm with specific energy input of 0.18–0.25 kWh/kg, followed by underwater strand pelletising. The formulation is PP homopolymer 80–94 wt%, SEBS compound 5–15 wt%, antioxidant masterbatch 0.1–0.3 wt%, and optionally linear low-density polyethylene 0–5 wt% to improve gloss retention. Comparative data are generated under ASTM D256-23 Izod notched impact at 23°C and -20°C, ASTM D638-22 tensile properties, and ISO 1133-1:2022 melt flow rate at 230°C/2.16 kg. Downstream production includes injection moulding of thin-wall parts with tonnage calculated at 3–5 kN/cm² projected area, using mould temperatures of 20–60°C. Terminal finished product types include automotive interior trim, appliance housings, storage containers, and battery cases. Published data for this specific compound in PP is limited; the values below represent comparable SEBS impact-modifier benchmark ranges and should be confirmed by line trials.
| SEBS addition (wt%) | Notched Izod at 23°C (J/m) | MFR at 230°C/2.16 kg (g/10 min) | Process observation |
|---|---|---|---|
| 0 (control) | 20–30 | 12–18 | Brittle failure at -20°C |
| 5 | 45–65 | 10–15 | Impact improvement; slight haze |
| 10 | 80–120 | 8–13 | Balanced impact/flow for thin-wall sections |
| 15 | 140–200 | 6–11 | Surface tack increases; side feeder uniformity critical |
Hot-melt adhesive formulation lines using 200–500 L sigma-blade mixers and slot-die coating at 160–190°C use Kraton™ G2708 GU-N as the elastomeric backbone in pressure-sensitive adhesives where permanent tack and low-temperature mandrel bend are specified. The elastomer addition ratio is 15–25 wt%, combined with 40–60 wt% hydrogenated C5/C9 hydrocarbon tackifier, 20–30 wt% paraffinic or naphthenic oil, and 0.5–1.0 wt% hindered phenolic antioxidant. Mixing is performed under nitrogen blanket for 60–120 min until a Brookfield Thermosel viscosity plateau is reached; the adhesive is then pumped through a heated transfer line to a slot-die coater at 175–185°C. Compliance for dry food-contact applications is anchored to FDA 21 CFR 175.105 adhesives, and adhesive performance is tested under ASTM D3330/D3330M peel adhesion and ASTM D3654/D3654M shear adhesion failure temperature. Aromatic oil content above 5 wt% should be avoided because it disrupts the styrene domains and reduces cohesive strength; PET carrier webs require corona treatment of 38–42 dyn/cm because the non-polar SEBS surface shows limited wetting. Terminal finished product types include hygiene article construction adhesives, disposable medical dressing fixation layers, label stocks, and carton sealing hot melts.
In halogen-free cable jacketing, Kraton™ G2708 GU-N is formulated at 20–40 wt% with polypropylene/polyethylene carrier 20–40 wt%, magnesium hydroxide or aluminium hydroxide flame retardant 30–50 wt%, and processing lubricant 1–3 wt%. The downstream production sequence starts with flame-retardant predispersion in a co-rotating twin-screw compounder at 150–180°C to prevent screw build-up, followed by pelletising and final jacketing extrusion on a 45–90 mm single-screw extruder with L/D 25:1 to 30:1. Melt temperature in the die is held at 150–190°C; a 80–120 mesh breaker plate removes agglomerates above 100 µm. Compliance is verified against IEC 60332-1-2:2015 vertical flame propagation, IEC 60754-1 halogen acid gas content, RoHS 2011/65/EU Annex II, and UL 1581 for tensile elongation before and after 7 days at 136°C. The low-temperature ductility of the jacket is checked by IEC 60811-401 cold bend at -40°C. Terminal finished product types include flexible appliance cords, automotive harness sheathing, photovoltaic cable jackets, and industrial control cable sheaths.
| Requirement | Standard/method | Typical acceptance value |
|---|---|---|
| Vertical flame propagation | IEC 60332-1-2:2015 | Char height ≤ 425 mm above lower edge |
| Halogen acid gas content | IEC 60754-1 | HCl equivalent < 5 mg/g |
| Hot tensile retention after 7 d at 136°C | UL 1581 | Tensile retention ≥ 70% of original |
| Cold bend at -40°C | IEC 60811-401 | No cracks |
Foamed SEBS footwear components are produced on injection moulding machines with physical blowing agent dosing or chemical blowing agent masterbatch injection. Kraton™ G2708 GU-N is used at 50–70 wt% with PP 10–20 wt%, mineral oil 10–20 wt%, silica or calcium carbonate filler 10–20 wt%, and azodicarbonamide chemical blowing agent at 0.3–0.8 phr. The production process uses barrel temperatures of 170–200°C, mould temperature 20–50°C, and fast injection speed to promote cell nucleation; part weight reduction of 15–30% relative to solid mouldings is the primary control metric. Published data for G2708 GU-N-specific microcellular expansion ratios remains limited, so line trials should bracket blowing agent content in 0.1 phr steps and record part weight, Shore A hardness under ISO 868:2003, abrasion loss under DIN 53516, and compression set under ASTM D395-21. Compliance for footwear consumer goods typically includes REACH Annex XVII restricted substance screening and RoHS 2011/65/EU restricted metals where electronic components are not present. Terminal finished product types include lightweight sandals, midsoles, insoles, and slipper soles.
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Kraton Kraton™G SEBS-Comp. G2708 GU-N is a pelletised styrene-ethylene/butylene-styrene thermoplastic elastomer supplied as a pre-compounded formulation. The material belongs to the styrenic block copolymer class defined in ISO 18064 and derives its elastomeric recovery from the thermodynamic incompatibility of polystyrene end-blocks and the saturated ethylene-butylene midblock. At ambient temperature, the polystyrene domains act as physical crosslinks; above the styrene glass transition, the material softens sufficiently to flow under shear. The compounded form is differentiated from neat SEBS by controlled additive incorporation and pellet geometry, allowing direct gravimetric feeding into single-screw and twin-screw equipment. Grade-specific hardness and melt-flow values must be taken from the current manufacturer certificate of analysis, because formulation adjustments can shift Shore A hardness and melt mass-flow rate without changing the grade designation. The absence of midblock unsaturation gives markedly lower oxidative chain scission than styrene-butadiene-styrene grades under sustained thermal load.
The principal difference is the compounded, finished-feedstock state. Neat SEBS powders or pellets require separate oil extension and antioxidant dosing on the compounding line; an error in oil add-on can shift Shore A hardness by several points. In SEBS compounds, paraffinic white oils are selectively absorbed by the midblock, lowering hardness and increasing melt flow. G2708 GU-N is delivered with the stabiliser package already dispersed, reducing mixing-energy variability. Compared against unsaturated SBS, hydrogenation removes backbone double bonds; this improves resistance to ultraviolet and thermal-oxidative embrittlement. In ozone exposure under ASTM D1149 at 50 pphm and 40 °C with 20 % elongation, unsaturated SBS grades commonly develop surface cracking whereas saturated SEBS grades of comparable hardness do not. The tradeoff is that SEBS generally has higher melt viscosity than SBS at equivalent styrene content and requires higher processing temperatures, typically 190 °C to 230 °C. The polystyrene end-block content controls hardness and tensile strength; a higher styrene weight fraction raises modulus and lowers elongation, but the exact percentage in G2708 GU-N is grade-controlled. Hardness is reported under ASTM D2240-15, using a Type A durometer after 15 s on a 6.0 mm compression-moulded plaque. Tensile properties are measured under ISO 527-2:2012 at 500 mm/min for thermoplastic elastomer test specimens.
On a corotating twin-screw extruder with 40:1 L/D and vacuum venting, a representative compounding profile sets the feed throat at 170 °C, barrels 2–4 at 180 °C to 200 °C, barrels 5–7 at 200 °C to 220 °C, and the die head at 210 °C to 230 °C. Screw speeds should be adjusted to maintain specific mechanical energy in the region of 0.12 kWh/kg to 0.22 kWh/kg; higher specific energy can raise melt temperature beyond 250 °C, where endblock network integrity declines and gel formation increases. In injection moulding, the melt temperature should be set between 190 °C and 230 °C, with mould temperatures between 20 °C and 50 °C. Clamp force requirements of 0.40 kN/cm² to 0.70 kN/cm² of projected area are commonly sufficient for thin-walled parts. Gate land lengths below 0.5 mm and runner diameters above 3.0 mm reduce premature freeze-off and jetting. When regrind is used, the ratio should not exceed 20 wt% unless validated by melt-flow and tensile retention studies; each heat history shifts the paraffinic process oil balance and can increase hardness and viscosity. Pre-drying at 60 °C for 2 h is required when pellet surfaces show condensation at relative humidity above 60 %. Valve-gated hot runners should be evaluated for hold-pressure leakage because low-viscosity compounded SEBS can flash between gate stem and bushing if the thermal expansion allowance is insufficient.
| Property | Standard method | Test condition | Reporting unit |
|---|---|---|---|
| Hardness | ASTM D2240-15 | 23 °C, 15 s, Type A | Shore A |
| Tensile strength | ISO 527-2:2012 | 500 mm/min, Type 5A | MPa |
| Elongation at break | ISO 527-2:2012 | 500 mm/min | % |
| Specific gravity | ISO 1183-1:2019 | 23 °C, immersion | g/cm³ |
| Melt mass-flow rate | ISO 1133-1:2022 | 230 °C, 5 kg | g/10 min |
| Compression set | ASTM D395 Method B | 70 °C, 22 h | % |
At the melt-conditioning stage, quality control must distinguish between compound viscosity shift and degradation. Capillary rheometry data at 230 °C over shear rates of 100 s⁻¹ to 1000 s⁻¹ provide better lot-to-lot resolution than single-point melt mass-flow rate. A decline in apparent viscosity at constant shear rate can result from molecular weight reduction or excess process oil, whereas an increase can indicate endblock oxidative coupling or additive migration. The G2708 GU-N product is supplied with a manufacturer-stabilised additive package, but high-shear dispersion of colour masterbatch can locally increase melt temperature and reduce plate-out. Static dissipative and slip additives should not be combined with amine-based stabiliser systems if surface bloom is critical, because the styrenic endblock phase shows limited compatibility with many amine chemistry species.
Applications for G2708 GU-N include soft-touch grips, automotive interior components, profiles, and consumer goods requiring low leachable mass. The saturated midblock gives lower leachable mass compared to SBS formulations, but food-contact status must be confirmed under the applicable jurisdiction. In the European Union, materials intended for food contact must meet Regulation (EU) No 10/2011; in the United States, 21 CFR 177.1810 covers styrenic block copolymers, but the final compounded article must still be tested by the converter. Adhesion to polypropylene substrates in two-shot moulding is primarily mechanical and melt-temperature dependent; substrate surface temperatures should exceed 120 °C for polypropylene to prevent premature interfacial solidification. For overmoulding onto ABS, chemical compatibility limits the use of plasticising oils that can migrate into the ABS styrene-acrylonitrile phase and induce environmental stress cracking at the substrate surface. Pre-drying of the substrate at 80 °C for 2 h and the use of mould surface textures above 25 µm Ra improve adhesion consistency. Outdoor exposure should be screened under ASTM G154 or ISO 4892-2 using the intended final part thickness and colour package, because ultraviolet absorber efficiency in thick sections differs from that in plaque specimens.
Thermoplastic vulcanisates retain lower compression set at elevated temperature than most uncompounded SEBS materials because the vulcanised rubber phase is covalently crosslinked. A compounded SEBS such as G2708 GU-N relies on polystyrene endblock physical crosslinks, which weaken progressively above 80 °C to 100 °C. Compression set measured under ASTM D395 Method B at 70 °C for 22 h is therefore the primary screening parameter. If the application requires a compression set below 35 % after 70 °C/22 h, the SEBS compound is generally outside the stable operating window; if the requirement is below 20 %, a thermoplastic vulcanizate or thermoset elastomer is required. For continuous dynamic loading, the service temperature should not exceed 70 °C unless the specific compound has been evaluated for creep and stress relaxation. At temperatures above 120 °C, the polystyrene domains soften significantly and part shape recovery is reduced. Chemical exposure to ketones, esters, and aromatic hydrocarbons causes swelling and must be screened according to ISO 1817 with the intended service fluid. Published data for this specific configuration is limited; therefore, end-use qualification under the full loading spectrum is required rather than reliance on generic SEBS chemical-resistance tables.