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Kraton Kraton™G SEBS-Comp. G2832 GS-N

    • Product Name: Kraton Kraton™G SEBS-Comp. G2832 GS-N
    • Factroy Site: Yinchuan, Ningxia, China
    • Price Inquiry: sales8@ascent-chem.com
    • Manufacturer: Ascent Petrochem Holdings Co., Limited
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    Specifications
    HS Code 983656
    Polymer Type SEBS compound
    Appearance Translucent pellets
    Density 0.90 g/cm³
    Melt Flow Rate 20 g/10 min at 230 °C/2.16 kg
    Shore A Hardness 35
    Tensile Strength At Break 5.5 MPa
    Elongation At Break 600%
    100 Modulus 1.5 MPa
    Tear Strength 20 kN/m
    Compression Set 25%
    Vicat Softening Temperature 60 °C
    Processing Method Injection molding
    Color Natural

    As an accredited Kraton Kraton™G SEBS-Comp. G2832 GS-N factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Kraton G2832 GS-N is supplied in moisture-protected 25 kg polyethylene bags, palletized at 1,000 kg per pallet.
    Container Loading (20′ FCL) Container Loading (20′ FCL): 20′ FCL loaded with Kraton™G SEBS-Comp. G2832 GS-N, palletized, secured, and sealed for ocean shipment.
    Shipping Kraton G SEBS-Comp. G2832 GS-N is a non-hazardous thermoplastic elastomer compound, typically shipped as pellets in 25-kg moisture-barrier bags or bulk containers. Keep dry, below 40°C, away from direct sunlight and ignition. Not regulated as dangerous goods for transport.
    Storage Store in a cool, dry, well-ventilated area, away from direct sunlight, heat, ignition sources, flames, and strong oxidizing agents. Keep containers tightly closed, properly labeled, and protected from moisture, dust, and contamination. Handle carefully to avoid bag damage; use first-in, first-out rotation. Maintain good housekeeping and follow the manufacturer’s SDS and local regulations.
    Shelf Life Shelf life is typically 24 months from date of manufacture when stored unopened in original packaging under dry, moderate conditions.
    Application of Kraton Kraton™G SEBS-Comp. G2832 GS-N

    When Kraton G2832 GS-N is substituted for an unsaturated SBS in melt conversion, the hydrogenated mid-block removes pendant unsaturation that otherwise initiates radical chain scission during high-shear compounding. The practical consequence is not a simple viscosity increase but a reduced reliance on shear heating to reach melt homogeneity; screw configurations that rely on excessive helix-angle mixing generate local temperatures above 220 °C, at which point the polystyrene domains lose their ability to re-form as discrete reinforcing nodes during quench. Downstream processing windows therefore shift toward narrower shear-rate envelopes, and each application must be evaluated against the most restrictive combination of dimensional stability, sterilisation resistance, and regulatory migration.

    What happens to tube ovality when peristaltic pump segments are sterilised at 121 °C and flexed under ISO 8536-4 saline backpressure?

    Medical fluid delivery tubing fabricated from Kraton G2832 GS-N is typically extruded without a separate compounding step, provided the line is fitted with a grooved-feed section and a vacuum vent at −0.08 MPa to remove residual moisture and low-molecular-weight oil. For Shore A hardness between 45 and 65, the grade is let down with polypropylene and a USP-grade white mineral oil using a single-screw extruder with 25:1 L/D and a compression ratio of 2.5:1; melt-temperature control is held between 195 °C and 210 °C because die swell increases below 190 °C and the tube wall becomes prone to chatter above 215 °C. A typical failure mode on production-scale single-screw lines is unstable melt pressure caused by pellet bridging in the feed throat when ambient temperature exceeds 30 °C without hopper cooling. Post-extrusion annealing at 60 °C for 30 min reduces subsequent ovality drift under peristaltic compression. Regulatory contact is anchored to FDA 21 CFR 177.1810 for the base styrene block polymer when formulated with permitted modifiers, while cytotoxicity is assessed by ISO 10993-5 and hemolysis for blood-contact adjunct components follows ISO 10993-4. Steam autoclave cycles at 121 °C for 30 min can raise Shore A hardness by 2–4 points after five cycles, which is relevant for reusable pump cassettes; gamma irradiation at 25–40 kGy produces minor yellowing but tensile strength retention after ISO 37 and ASTM D638-14 testing normally exceeds 90%. Published data for electron-beam irradiation of this exact pre-compound at doses above 50 kGy is limited. Representative end products include peristaltic pump segments, pressure monitoring lines, and enteral feeding tube connectors where phthalate-free construction is a purchasing constraint.

    In co-rotating twin-screw compounding at L/D 40:1, Kraton G2832 GS-N is typically introduced at the main feed throat while oil is injected after the melting zone to prevent torque spikes. Automotive soft-touch sheet formulations use 20–40 wt% Kraton G2832 GS-N, a polypropylene carrier, and a paraffinic oil; hardness is adjusted across 30–80 Shore A by shifting the oil-to-polypropylene ratio rather than by changing the SEBS content alone. Twin-screw torque fluctuations above 5% during oil injection correlate with incomplete oil dispersion, which later appears as surface tack and elevated fogging values under VDA 278. Low total volatile organic content is measured under VDA 278 and fogging under DIN 75201, with typical automotive interior specifications requiring condensate below 2 mg. Sheet extrusion on a calendar line uses melt temperatures of 190–220 °C and roll-stack temperatures of 30–60 °C; the lower roll temperature is critical because the polystyrene end-blocks must solidify before the ethylene-butylene mid-block relaxes to build compression set resistance. Scratch and mar performance relative to PVC skins is controlled by adding a high-molecular-weight polyether-modified siloxane at 1–3 wt%, and surface mattness is generated by embossing rather than by filler addition, which would increase density. Representative end products are instrument-panel skins, door roll tops, and centre-console bolsters where low fogging and low odour are mandatory.

    Halogen-free charge-cable jacketing with flame-retardant fillers above 60 wt%

    Flexible EV charging cables specified under EN 50620:2017 force a trade-off between high filler loading for flame retardance and the elongation retention required by flex testing. Kraton G2832 GS-N is used as the resilient phase in a polypropylene/SEBS jacket compound containing magnesium hydroxide at 60–65 wt%; at this loading, the compound’s melt viscosity under ISO 1133-1 conditions is highly shear-sensitive, and operation on a co-rotating twin-screw extruder with L/D 44:1 requires deep-flighted conveying elements in the filler-intake zone to avoid barrel temperatures above 220 °C. Local temperature excursions above 230 °C cause magnesium hydroxide to liberate water, which produces surface pitting and lowers the breakdown voltage measured under IEC 60243-1. On production-scale lines running continuous jackets for over 12 h, die-lip deposits from filler moisture interaction with the SEBS mid-block are controlled by pre-drying magnesium hydroxide at 90 °C for 4 h and by applying a 0.5–1.0 wt% stearate processing aid. Jacket extrusion uses a 3:1 compression-ratio screw and a melt temperature of 190–210 °C; haul-off tension is kept below 8 N/mm² cross-sectional stress to avoid necking the soft phase. Mechanical acceptance is anchored to UL 1581 tensile and elongation requirements, while the end-product cable must also meet cold impact at −25 °C and abrasion resistance under ISO 6722-1 where applicable. Material composition is screened against RoHS Recast 2011/65/EU and REACH SVHC obligations. Oil resistance of this polyolefinic compound is inferior to thermoplastic polyurethane jackets; contact with mineral oil at 60 °C above 7 days is outside the recommended operational boundary. Representative end products are flexible EV charging cables, power-tool cords, and outdoor appliance leads where halogen-free construction is specified.

    Adding Kraton G2832 GS-N to a polypropylene homopolymer at 10–30 wt% in a twin-screw extruder creates a dispersed SEBS phase whose particle sizing is governed by the ratio of interfacial tension to local shear stress. Impact modification is evaluated under ISO 180/A notched Izod and ISO 527-1 tensile testing; the practical ceiling is not a fixed percentage but the point at which discrete SEBS domains begin to coalesce into an interpenetrating network, which in typical high-viscosity PP occurs near 35 wt%. At 50 wt% the compound behaves as a thermoplastic elastomer rather than an impact-modified polyolefin, with a discontinuous drop in flexural modulus measured under ISO 178. Compounding on a co-rotating twin-screw line with L/D 36:1 and under water-ring pelletising is preferred because strand pelletising of high-oil formulations can generate pellet agglomeration in the classifier. Injection moulding of these modified PP grades uses melt temperatures of 200–230 °C and a clamp force based on projected area; thin-wall parts below 1.5 mm wall thickness require higher mould temperatures to restore surface gloss after texture etching. Representative end products are polyolefin automotive storage bins, appliance housing corners, and battery-pack structural brackets where low-temperature ductility below −10 °C is required.

    Slot-die coating of elastic laminate adhesives requires a complex-viscosity plateau between 160 °C and 180 °C that remains stable through a hot-melt tank residence time of 8–12 h. Kraton G2832 GS-N is compounded with a hydrogenated hydrocarbon tackifier at a tackifier-to-polymer ratio of 0.8:1 to 1.2:1 and a naphthenic oil at 20–35 wt% of the total adhesive. The mixing vessel is a vertical dual-blade unit with bottom discharge and a jacket set at 170 °C; vacuum is applied at −0.09 MPa to remove entrained air because microbubbles cause lane splitting in the slot die. Spiral-tester viscosity at 160 °C is controlled within a narrow band, and peel adhesion to nonwoven substrates is measured by ISO 8510-2 after 24 h conditioning at 23 °C and 50% RH. Indirect food-contact status for the adhesive base may be supported under FDA 21 CFR 175.105 when the finished construction is not in direct contact with food or beverage. Adhesive transfer from the coating head to polyethylene backsheet is limited by the softening point of the tackifier; high-softening-point systems can degrade the styrene domains if the application head is run above 190 °C. End products are elastic waistbands for infant and adult incontinence articles, side-panel lamination, and medical dressing tapes. The material is not recommended for spray-grade low-viscosity hot-melt tunnels unless diluted to below 1,500 mPa·s, because the resulting melt elasticity at the nozzle becomes unmanageable during intermittent application.

    When insert overmolding on PC/ABS substrates demands low haul-off orientation

    Insert injection moulding of power-tool grips and personal-care appliance bodies uses Kraton G2832 GS-N as a soft-touch layer over rigid PC/ABS or PC/PBT substrates. The pre-compound is dried at 80 °C for 2–3 h when ambient relative humidity exceeds 60%, and barrel profile is set from hopper to nozzle at 170 °C, 190 °C, 200 °C, and 210 °C. Holding pressure is established by iterative short-shot studies on a 80-ton hydraulic press with a 20:1 L/D general-purpose screw; a cushion of 3–5 mm is maintained to avoid decompression at the check ring, which would otherwise entrain air at the substrate interface. Batch-to-batch variation in pellet surface oil can shift cushion position and lead to short shots; surface-oil levels above 0.3 wt% reduce feed consistency. Adhesion to PC/ABS is influenced by substrate surface temperature; preheating the insert to 80–100 °C improves wetting without requiring a tie layer. The overmoulded layer is evaluated by ISO 2409 cross-cut adhesion and by ISO 2813 gloss after textile abrasion, while hardness is measured by ISO 868 or ASTM D2240. A semimatte surface is achieved through mould texturing; gloss below 2 GU at 60° measurement geometry indicates sufficient replication. The principal processing limitation is melt orientation in the gate region: excessive injection velocity above 120 mm/s in thin sections produces anisotropic shrinkage that manifests as edge lift of the soft layer. Representative end products are drill-housing overmoulds, electric toothbrush handles, and handheld diagnostic instrument grips.

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    Certification & Compliance
    More Introduction

    The product designation Kraton Kraton™G SEBS-Comp. G2832 GS-N identifies a pre-compounded thermoplastic elastomer in which a saturated styrene–ethylene/butylene–styrene block copolymer is dispersed with a polyolefinic extender and a natural-tone stabilizer package. The G-series nomenclature separates this material from neat SEBS crumb. The suffix GS-N denotes the general-purpose natural stabilizer system, while the numeric designation G2832 distinguishes the grade by its melt rheology and hardness position. The compound is supplied as pellets for injection moulding, extrusion, and overmoulding of components requiring low Shore A hardness and polypropylene adhesion. Because the elastomer mid-block is fully hydrogenated, the material is less susceptible to oxidative chain scission than unsaturated SBS block copolymers. A lot-specific certificate of analysis should be obtained before process validation because melt flow rate and hardness are controlled within supplier statistical limits that may be narrower than generic third-party summaries. The exact property window for G2832 GS-N should be confirmed under ISO 868, ISO 37, and ISO 1133-1:2022 before tooling trials.

    How does the compounded G2832 GS-N grade differ from neat G-series SEBS triblocks?

    Neat Kraton G-series SEBS triblocks are typically supplied as high-viscosity crumb or powder and require oil extension, filler addition, and high-shear dispersion before they develop useful physical properties. G2832 GS-N is pre-compounded so that the continuous polyolefinic phase lowers the injection-moulding melt viscosity while retaining the saturated mid-block elastic recovery. Under ISO 1133-1:2022, the compound commonly exhibits an MFR of 12–18 g/10 min at 230 °C and 2.16 kg. Unmodified SEBS of comparable styrene content often cannot be measured under the same conditions because its viscosity exceeds practical MFR limits. The pre-dispersion reduces the need for high-shear compounding on the converter’s line, but it also narrows the available formulation window for converters who wish to add independent oil or masterbatch. When natural SEBS is compounded at the converter, batch-to-batch hardness variability can exceed ±5 Shore A if mixing time is short. The supplier-compounded grade is typically controlled within tighter limits, but those limits should be verified from the certificate of analysis rather than assumed from class data.

    Compared with thermoplastic polyurethane elastomers of similar hardness, G2832 GS-N offers a lower-density profile in the 0.88–0.90 g/cm³ range and does not require dewpoint-controlled drying unless surface moisture exceeds 0.05 wt%. Thermoplastic vulcanizates based on EPDM/polypropylene can provide higher upper service temperatures, but soft grades below 35 Shore A often require higher shear and a narrower overmoulding temperature window. The selection between G2832 GS-N and these alternative elastomers should therefore be based on compression set under the actual service fluid and temperature, not on hardness alone.

    When G2832 GS-N is moulded on hydraulically clamped machines of 80–150 t clamp force, the conventional reciprocating-screw plasticating unit should maintain a compression ratio of 2.0:1 to 2.5:1 and a shot volume between 25% and 75% of barrel capacity. Melt temperatures measured by a pyrometer at the nozzle are typically held between 190 °C and 230 °C. Mould temperatures above 40 °C improve weld-line strength and reduce frozen-in orientation. Excessive residence time above 240 °C can produce gel formation and discoloration in natural-tone pellets. Pre-drying is advised when storage relative humidity exceeds 60%; a desiccant hopper dryer set to 80 °C for 2–4 h reduces surface moisture below 0.05 wt%. In production-scale validation of similarly soft SEBS compounds, inadequate venting at the mould parting line has been observed to cause gas-burn marks in thick grip sections. Vents of 0.02–0.05 mm land depth and 0.5 mm width are commonly used for this hardness class, but vent depth must be adjusted for tool steel and cavity pressure because excessive vent depth produces flash.

    When the compound is overmoulded onto isotactic polypropylene substrates

    G2832 GS-N is selected for overmoulding because the pre-compounded polyolefin-rich surface builds a melt bond with polypropylene through interdiffusion rather than adhesive primers. The substrate should be preheated to 50–70 °C before the second shot to minimize quench-induced delamination. Cavity pressure during packing should not exceed 60 MPa if the substrate is a thin-walled PP shell, because excessive packing compresses the first shot and increases sink marks. In contrast to unmodified SEBS, which can exhibit adhesive failure at the interface, the compounded grade’s compatibility with PP shifts failure toward cohesive tearing within the elastomer when the bond is properly formed. A peel test carried out according to ASTM D903-20 or a tensile lap-shear test under ISO 527-2:2012 can be used to screen bond performance. Published data for this specific configuration are limited, so adhesion trials with the actual substrate grade are required. Differences in PP nucleating agents, mould release, and corona treatment can alter bond strength by more than 30%, and the substrate surface should be free of silicone spray before overmoulding.

    For profile and tubing extrusion, a single-screw extruder with a length-to-diameter ratio of 24:1 to 30:1 and a polyolefin screw equipped with a low-shear mixing element is used. Barrel temperature profiles from feed to die should rise from 170 °C to 200 °C; the die temperature is maintained near 200–210 °C. The melt is non-Newtonian and pseudoplastic. An increase in screw speed from 20 min−1 to 80 min−1 does not produce a linear output gain because wall slip and shear heating become significant. Die swell is lower than for neat SEBS because the polyolefinic extender raises the critical shear rate. A water bath at 15–25 °C is used to freeze the profile, and a vacuum sizing tank with closed-loop pressure at 0.05–0.2 bar is preferred for precise tubing dimensions. Material pre-drying is required only if pellet surface moisture exceeds 0.05 wt%. Extrusion trials with G2832 GS-N should establish the actual melt pressure and motor load against supplier limits; generic data for this grade are limited.

    Compression set, thermal aging, and mid-block oxidative stability

    For applications that require sealing under static load, the compound is commonly characterized by compression set under ISO 815-1:2019. Typical values for SEBS compounds in the 30–35 Shore A range fall near 30% after 22 h at 70 °C, but the exact G2832 GS-N value must be taken from the manufacturer’s datasheet. The fully hydrogenated mid-block gives better resistance to oxidative degradation than SBS, but the material is not a thermoset. Continuous service above 90 °C is not recommended unless the part is tested for compression set and tensile retention under ISO 188:2011. When improved high-temperature oil resistance is required, a sulfonated or grafted SEBS grade may be necessary. The compound is not suitable for prolonged immersion in strong organic solvents, aromatic oils, or chlorinated hydrocarbons, because such fluids plasticize the styrenic domains and reduce tensile strength below acceptable limits.

    The following test methods are used for incoming resin release and periodic process capability studies. The table does not replace the lot-specific certificate of analysis.

    PropertyTest methodTypical class rangeRelevance to G2832 GS-N processing
    HardnessISO 86830–35 Shore AConfirms low plateau modulus for soft-touch grips and seals
    DensityISO 1183-1:20190.88–0.90 g/cm³Used for shot-weight and cost-per-part calculations
    Tensile strength at breakISO 374.0–5.0 MPaIndicates cohesive strength in thin cross-sections
    Elongation at breakISO 37500–650%Indicates strain capacity before brittle failure
    Tear strengthISO 34-115–20 kN/mScreens notch sensitivity near edge gates and weld lines
    Melt flow rateISO 1133-1:202212–18 g/10 min at 230 °C/2.16 kgCorrelates with filling pressure and overmoulding penetration
    Compression setISO 815-1:201925–35% after 22 h/70 °CIndicates recovery under continuous static load

    Quality release for G2832 GS-N should include capillary rheometry at 230 °C across apparent shear rates from 100 s−1 to 1000 s−1 because the MFR method provides only a single-point viscosity. The power-law index for similar SEBS compounds is commonly below 0.5. This pseudoplasticity means that doubling the injection pressure does not double flow length. Processors should measure actual cavity pressure with pressure transducers rather than relying on machine hydraulic setpoints. Gate freeze time can be estimated from the pellet solidification rate. For soft SEBS compounds, gates below 1.0 mm diameter can freeze before packing is complete, causing sink marks and dimensional variation. A gate diameter of 1.0–1.5 mm and a land length of 0.5–1.0 mm are commonly used for soft-touch grips.

    Regulatory screening and storage stability should not be inferred from differential scanning calorimetry alone

    The stabilization package of G2832 GS-N is intended for natural-tone processing, but colour masterbatches and processing aids can interact with the pre-dispersion. For medical or food-contact evaluations, the converter must verify the specific supplier regulatory statement against applicable frameworks such as FDA 21 CFR 177.2600 for rubber articles used in food contact or EU 10/2011 for plastics intended for food contact. Compliance is grade-specific and cannot be assumed from SEBS class membership. The saturated backbone improves UV and oxidative stability relative to SBS, but prolonged outdoor exposure can still yellow natural-tone parts. Storage in sealed, moisture-resistant packaging at ambient temperature below 40 °C is recommended. Exposure to direct sunlight or high humidity can cause surface condensation and moulding defects. The pelletized compound should not be blended with amine-containing masterbatches that can accelerate oxidation or with free-flowing plasticizers that can shift Shore A hardness outside the intended process window. A differential scanning calorimetry thermogram can identify styrenic domain transition temperatures, but it does not replace mechanical property tests because morphology is sensitive to shear history and nucleating additives.

    In injection moulding, surface defects observed during production validation of similar SEBS compounds include jetting at gate velocities above 300 mm/s, gate blush from undersized cold slugs, and flow marks caused by melt-temperature differences greater than 10 °C across the melt stream. G2832 GS-N should be processed with a cold slug well and a sprue break to prevent cold material from entering the cavity. For multi-cavity tools, runner balancing must be checked because the pseudoplastic melt preferentially fills shorter runner paths, leading to cavity-to-cavity hardness variation. The saturated ethylene/butylene mid-block also provides low-temperature flexibility, because the glass transition of the saturated rubber segment is below −40 °C when measured by differential scanning calorimetry at 10 °C/min.

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