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SINOPEC Baling Hunan SBS YH-898

    • Product Name: SINOPEC Baling Hunan SBS YH-898
    • 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 692323
    Polymer Type Styrene-butadiene-styrene block copolymer (SBS)
    Structure Linear
    Oil Extension Oil-extended
    Appearance White or light-yellow pellets
    Styrene Content 30%
    Oil Content 20%
    Volatile Matter ≤1.0%
    Ash ≤0.20%
    Tensile Strength ≥10.0 MPa
    Elongation At Break ≥700%
    300 Modulus ≥2.0 MPa
    Shore A Hardness 55–70
    Melt Flow Rate 0.5–5.0 g/10 min
    Density 0.94–0.96 g/cm³
    Mooney Viscosity Ml 1 4 100 C 20–50

    As an accredited SINOPEC Baling Hunan SBS YH-898 factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing SINOPEC Baling Hunan SBS YH-898 is supplied in 25 kg woven bags, typically 40 bags (1,000 kg) per pallet.
    Container Loading (20′ FCL) SINOPEC Baling Hunan SBS YH-898 loaded in a 20′ FCL container, bagged and securely stowed for ocean shipment.
    Shipping SINOPEC Baling Hunan SBS YH-898 is a solid styrene-butadiene-styrene block copolymer, non-hazardous and not regulated for transport. It is shipped in 25 kg woven bags on pallets. Store in a cool, dry, ventilated area; protect from moisture, heat, sunlight, and bag damage.
    Storage Store SINOPEC Baling Hunan SBS YH-898 in a cool, dry, well-ventilated area away from direct sunlight, heat, sparks, and open flames. Keep in tightly closed original packaging on pallets; prevent moisture, dust, oil, and chemical contamination. Avoid heavy stacking and prolonged high-temperature or UV exposure to reduce aging and caking. Inspect containers regularly and follow local regulations and the manufacturer’s SDS.
    Shelf Life SINOPEC Baling Hunan SBS YH-898 has a typical shelf life of 12 months when stored cool, dry, and sealed.
    Application of SINOPEC Baling Hunan SBS YH-898
    Dissolution of linear SBS YH-898 into paving-grade bitumen is governed by shear-induced particle size reduction followed by solvent swelling of the butadiene midblock. Integration does not proceed via simple stirring; a rotor-stator high-shear mill or colloid mill is required to reduce polymer domain size below the threshold where network formation becomes continuous. In reference production batches, bitumen is preheated to 160–165 °C before polymer addition at 3–7 wt% for paving applications and 10–15 wt% for waterproofing membranes. The high-shear unit operates with tip speeds between 4,000–6,000 rpm and a colloid mill gap set at 0.25–0.50 mm. Polymer is fed incrementally over 15–30 minutes to avoid agglomerate formation. Temperature must not exceed 185 °C; the butadiene segment undergoes thermal degradation above this threshold, producing a measurable drop in elastic recovery. Completion of dispersion is confirmed by fluorescent microscopy with a polymer phase continuity target above 90%.Storage stability of unmodified SBS-bitumen blends deteriorates when polymer loading exceeds 12–15 wt%. Polystyrene domains aggregate under static heated storage, leading to phase separation within 72 hours at 160 °C. Sulfur crosslinking at 0.1–0.2 wt% extends storage stability beyond 7 days without gelation during subsequent membrane manufacturing. Crosslinked systems achieve elastic recovery above 75% under ASTM D6084, compared with recovery frequently below 50% for uncrosslinked reference blends. Ring-and-ball softening point (ASTM D36) shifts from base bitumen values near 48–52 °C to 115–125 °C in membrane-grade formulations containing 12 wt% polymer. Low-temperature flexibility for torch-applied membranes is assessed at -20 °C bend conditions under EN 1109. Paving-grade modified binders are specified under EN 14023 and AASHTO M332; terminal grades commonly fall within PG 70-28 or PG 76-22. End products include torch-applied SBS waterproofing membranes conforming to GB/T 23457, bridge deck waterproofing systems, and gap-graded stone matrix asphalt wearing courses for heavy-traffic roadways.

    High-Shear Sole Compounds and Oil Loading Windows

    Compound formulation for injection-molded unit soles begins with staged addition in an intermeshing internal mixer, typically a Banbury-type unit of 55–75 L net chamber volume. Linear SBS YH-898 is masticated first with crystallizable polystyrene resin at 125–135 °C to break the polystyrene domain structure. Naphthenic or paraffinic process oil at 30–60 phr is then introduced in three equal increments. Each oil increment is followed by 30–45 seconds of ram-down mixing to maintain sufficient shear for oil absorption. Total cycle time ranges from 10–14 minutes; dump temperature is controlled at 140–155 °C. Discharge is transferred to a two-roll mill at 60–70 °C for final dispersion and sheeted for granulation. Filler addition, predominantly calcium carbonate or precipitated silica at 0–25 phr, is made during the final oil increment to minimize dust generation. Injection molding of the compounded pellets uses a reciprocating screw with 20:1 L/D, nozzle temperature set at 165–180 °C, and mold temperature maintained at 25–40 °C. Clamp force for multi-cavity sole molds typically falls between 120–180 tonnes; cycle time for a 6–8 mm sole cross-section is 45–70 seconds.The hardness response to oil loading follows a predictable but non-linear curve because oil selectively solvates the butadiene midblock. The following reference formulation gradient, derived from published linear SBS footwear compound data, illustrates the practical operating window. Tensile strength under ASTM D412 for oil-filled SBS sole compounds generally falls between 8–15 MPa, with elongation at break from 400–800%. Compression set measured under ASTM D395 at 70 °C for 22 hours ranges from 30–55%, a limitation in comparison with vulcanized rubber for high-load footwear. Slip resistance is tested under SATRA TM77; compounds with Shore A below 45 frequently require a harder outsole co-molding to pass wet-slip thresholds. Direct-attach construction allows the SBS midsole to be injected directly onto the leather or textile upper without adhesive film, provided the upper is pre-treated with a halogenated primer. End products include lightweight unit soles, direct-attach safety footwear midsoles, microcellular foam saddles, and expandable compounds blown with azodicarbonamide at 0.5–1.5 phr using a chemical blowing agent decomposition window of 200–215 °C.
    Target Shore A (ASTM D2240)SBS Y (phr)PS Resin (phr)Process Oil (phr)CaCO₃ Filler (phr)
    35–401002055–600
    45–501003040–5010
    55–601003530–4015–20
    65–701004020–3025

    What Limits High-Temperature Shear Resistance in SBS Hot-Melt PSAs?

    The upper service temperature of an SBS-based hot-melt pressure-sensitive adhesive is governed less by the polymer styrene content than by the glass transition temperature of the polystyrene end-blocks and the dilution effect of the tackifier. At ambient temperature, the polystyrene domains act as physical crosslinks. Once the adhesive film reaches 80–95 °C, these domains soften and the network loses cohesive strength. Shear adhesion failure temperature (SAFT) determined under ASTM D4498 for C5-tackified linear SBS formulations typically falls between 65–85 °C. A representative hot-melt formulation contains 25–35 parts linear SBS, 45–55 parts C5 aliphatic or C9 aromatic hydrocarbon tackifier resin, 15–25 parts naphthenic process oil, and 1–2 parts hindered phenolic antioxidant. Mixing is carried out in a sigma-blade kneader or heated turbine mixer at 145–165 °C under a full nitrogen blanket. Residence time beyond 60 minutes at temperature produces measurable viscosity drift and gel formation, particularly when the formulation contains unsaturated C5 resins without antioxidant protection. Viscosity at 160 °C must remain within 4,000–20,000 mPa·s for slot-die or roll coating; values above this window require heated hose and manifold modifications.Solvent-borne SBS contact adhesives represent a separate processing route. Typical solids content is 22–30 wt% dissolved in a toluene / SBP 80/110 blend at 50:50 ratio. Solution viscosity at 25 °C falls between 2,000–5,000 mPa·s. Application is performed via knife-over-roll or comma coater onto release liner or directly onto packaging film. Open time before lamination is governed by solvent evaporation rate; fast toluene evaporation shortens open time to 10–20 seconds, while SBP 80/110 extends open time to 30–60 seconds. Peel adhesion under ASTM D3330 for a 25 µm dry adhesive film on polyester laminate generally ranges from 8–20 N/25 mm. Loop tack under ASTM D6195 for the same film falls between 6–15 N. End products include packaging carton sealing tapes, label stock, protective film for stainless steel panels, and repositionable note adhesives. Food-contact laminate adhesives require compliance with FDA 21 CFR 175.125, which covers pressure-sensitive adhesives intended for food packaging use, with migration testing under simulated food conditions specified by the end-use temperature.Twin-screw compounding of SBS YH-898 into polypropylene homopolymer or copolymer matrices produces a dispersed rubber phase with domain sizes between 0.5 µm and 2.0 µm when processed under appropriate shear. A co-rotating twin-screw extruder with L/D 36:1 to 48:1, screw speed 300–600 rpm, and barrel temperature profile 180–220 °C for PP carrier is employed. SBS addition at 5–15 wt% shifts the failure mechanism from brittle fracture to shear yielding. Notched Izod impact resistance under ASTM D256 increases from 2–4 kJ/m² for unmodified PP homopolymer to 8–20 kJ/m² at 10 wt% SBS loading. Flexural modulus measured under ASTM D790 decreases in approximately linear proportion to rubber content, with a 10 wt% SBS loading typically reducing modulus by 20–30% relative to the neat matrix. Interfacial adhesion between SBS and PP is incomplete; some reference formulations incorporate maleic anhydride-grafted PP at 1–3 wt% to reduce dispersed phase coalescence during subsequent injection molding. Without compatibilizer, injection-molded parts exhibit surface delamination at weld lines under flexural stress. End products include automotive interior trim panels, appliance housing components, and blow-molded luggage shells where low-temperature impact resistance is required at -20 °C service conditions.

    Mechanical Shear Degradation Is Quantified via ASTM D6278

    Application of SBS YH-898 as a viscosity index improver requires a pre-dissolved concentrate because direct addition to finished lubricant at ambient temperature results in incomplete solvation and pump blockage. A representative concentrate contains 10–15 wt% SBS in paraffinic base oil of 100 SUS viscosity at 40 °C, stirred at 120–140 °C for 4–6 hours under nitrogen until full clarity is achieved. Final lubricant polymer concentration is 0.5–3 wt%. Kinematic viscosity improvement is evaluated under ASTM D445 at 40 °C and 100 °C, with viscosity index calculated per ASTM D2270. Mechanical shear degradation is tested using the diesel injector nozzle procedure of ASTM D6278 or the equivalent DIN 51382 tapered roller bearing test. Permanent shear stability index for linear unsaturated SBS typically falls between 30–60, which is inferior to hydrogenated styrenic block copolymers but adequate for industrial gear oils and greases where service temperatures remain below 80 °C. Published data for YH-898 in this specific configuration is limited; formulation work should include a shear-stability confirmation batch prior to commercial qualification. End products are limited to industrial gear oil viscosity modification and grease thickener adjustment, not automotive crankcase formulations where oxidative stability requirements exceed unhydrogenated SBS capability.

    If YH-898 Is Selected for Skin-Contact Elastomeric Components

    Selection of SBS YH-898 for toy, infant-care, or medical device components imposes migration testing under simulated gastric fluid conditions and extractables profiling. Compounding for these applications must exclude vulcanizing agents, amine-based stabilizers, and aromatic process oils. Plasticizer selection shifts to white mineral oil complying with USP/NF monograph requirements. Heavy metal content at raw material level must support finished article compliance with EN 71-3:2019+A1:2021 migration limits for 19 elements. Processing for injection-molded parts is performed at 175–210 °C using a low-compression screw, mold temperature 25–50 °C, and food-grade silicone emulsion release agents. Post-molding extractables are quantified by total immersion in n-heptane under EU 10/2011 conditions; typical results must remain below the overall migration limit of 10 mg/dm². Cytotoxicity screening under ISO 10993-5 uses L929 mouse fibroblast cells with viability threshold above 70%. Irritation and sensitization potential is assessed under ISO 10993-10. The raw polymer must be covered under FDA 21 CFR 177.1810 for styrene block polymers intended for food-contact use. Heavy metal, phthalate, and brominated flame retardant restrictions under RoHS 2011/65/EU apply when the component is incorporated into electrical or electronic equipment housings.Repeated autoclave sterilization above 121 °C is not recommended because the polystyrene domains undergo progressive coalescence that reduces tensile recovery. Single ethylene oxide cycles at 55 °C and humidity below 70% RH are tolerated with less than 10% change in Shore A hardness. Because SBS YH-898 contains unsaturated butadiene segments, it is incompatible with prolonged exposure to strong oxidizing agents, ozone-generating environments, and mineral-oil-based printing inks that cause surface tack development. The following compliance matrix consolidates the applicable testing framework.
    Test StandardParameterThreshold or Method Condition
    FDA 21 CFR 177.1810Styrene block polymer food contactExtraction limits per end-use temperature
    EU 10/2011Overall migration< 10 mg/dm²
    EN 71-3:2019+A1:2021Element migration from toys19 elements, category-specific limits
    ASTM F963Toy safety, heavy metalsSoluble element limits per substrate
    ISO 10993-5CytotoxicityL929 viability ≥ 70%
    ISO 10993-10Sensitization, irritationNo erythema or edema grade ≥ 1
    RoHS 2011/65/EUPb, Cd, Hg, Cr(VI), PBB, PBDEHomogeneous material limits
    REACH EC 1907/2006SVHC declarationCandidate list 0.1 wt% threshold
    End products within this compliance envelope include teething rings, pacifier handle over-molding, respiratory mask straps, disposable tourniquets, and blood pressure cuff tubing connectors.
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    Certification & Compliance
    More Introduction

    SINOPEC Baling Hunan SBS YH-898 is a styrene-butadiene-styrene block copolymer manufactured at the Baling petrochemical site in Hunan Province and supplied as porous pellets. The grade is positioned as a low-styrene triblock elastomer with a nominal bound styrene content of 30 wt%; the polybutadiene midblock remains unsaturated, which distinguishes the product from hydrogenated styrenic block copolymers such as SEBS. YH-898 is intended for bitumen modification, hot-melt adhesive compounding, polyolefin impact modification, and selected footwear compounds where melt processability must be balanced against low-temperature flexibility. The material is not an oil-extended grade, and the producer literature typically lists residual volatile matter below 1.0 wt%. Because the styrene end-blocks form a physical network through microphase separation, no vulcanisation step is required to develop tensile strength. This molecular architecture allows repeated melt processing, but it also limits continuous service temperature to below the order-disorder transition of the styrene domains. The specification envelope is controlled by ISO and ASTM methods, and batch-level certificates of analysis remain authoritative. The subsequent sections address the specification, comparative positioning, processing boundaries, and regulatory status of YH-898 without substituting for a current manufacturer datasheet.

    What specification envelope governs YH-898?

    Property Test method Unit Typical range or limit
    Bound styrene contentISO 2453:1991wt%28–32
    Tensile strengthISO 37:2017MPa≥ 18
    Elongation at breakISO 37:2017%≥ 700
    300% modulusISO 37:2017MPa1.5–2.5
    HardnessASTM D2240Shore A70–80
    Melt mass-flow rateISO 1133-1:2022g/10 min0.1–5.0 at 200 °C / 5 kg
    Volatile matterASTM D5668wt%≤ 1.0
    AshASTM D5667wt%≤ 0.2

    These values are typical data from manufacturer technical literature and are not batch-release limits. The certificate of analysis for a particular lot controls volatile matter, ash, and melt flow. Incoming inspection on compounding lines often adds a moisture check because porous pellets can adsorb atmospheric water. Storage at relative humidity above 60% can raise surface moisture to 0.1–0.3 wt%; hopper drying at 60–70 °C for 2–4 h is applied before extrusion. Drying temperature above 80 °C is avoided because it can cause pellet blocking in the hopper.

    Comparative positioning against higher-styrene and star-branched Baling SBS grades

    YH-898 is differentiated from YH-792 primarily by bound styrene content. Producer literature for YH-792 quotes a nominal styrene content of 40 wt%, which raises hardness to 85–90 Shore A under ASTM D2240 and increases tensile strength above 24 MPa under ISO 37. The higher styrene fraction also raises melt viscosity and reduces the compliance of the butadiene continuous phase at low temperature. YH-898, at 30 wt% styrene, exhibits lower modulus and lower hardness, which is advantageous for bitumen low-temperature crack resistance and for adhesive formulations needing soft hand feel. Against YH-796, another 30 wt% styrene grade in the Baling portfolio, YH-898 is selected where improved flow and shorter mixing cycles are required; the distinction is best verified by melt mass-flow rate measured at 200 °C / 5 kg per ISO 1133-1:2022. Star-branched SBS grades generally produce higher melt strength and elastic recovery in bitumen, but they can require longer high-shear dispersion and can raise extruder back pressure. YH-898, with a narrower molecular weight distribution as characterised by gel permeation chromatography, produces lower die swell in profile extrusion and more uniform pellet plastication in 25–75 mm co-rotating twin-screw extruders. The practical melt-pressure difference cannot be stated as a single value because screw geometry, die restriction, and throughput dominate; process verification on target tooling is required. When compared with SEBS, YH-898 has no saturated midblock, so oxidative resistance is lower but compatibility with bitumen and nonpolar tackifier resins is typically more direct.

    Hot-melt pressure-sensitive adhesive compounding with YH-898 typically charges the polymer at 15–35 wt% into a sigma-blade or planetary mixer along with 45–60 wt% C5/C9 hydrocarbon tackifying resin, 10–25 wt% naphthenic processing oil, and 0.5–1.0 wt% hindered phenolic antioxidant. The mixer jacket is held at 160–180 °C under nitrogen blanketing to limit midblock oxidation. Melt viscosity of the finished adhesive is measured with a Brookfield thermocell at 170 °C per ASTM D3236; typical values fall between 5,000 and 20,000 mPa·s, depending on tackifier chemistry and SBS addition level. Application through slot-die coaters using gear pumps is generally operated at 150–170 °C when formulation viscosity remains below 15,000 mPa·s. Peel adhesion to stainless steel is measured at 180° angle and 300 mm/min jaw separation per ASTM D903; the exact value is controlled by resin softening point and SBS loading rather than by the SBS grade alone. Loop tack is assessed per ASTM D6195. Because YH-898 is unsaturated, continuous adhesive lines should limit residence time at 170 °C to 8 h and use inert gas blanketing; otherwise viscosity drift and gel formation from crosslinking may appear.

    When dispersed into bitumen, shear history determines phase morphology

    Bitumen modification with YH-898 is typically conducted at 4–7 wt% polymer loading in a high-shear mill such as a Silverson L5T or an inline Siefer mill. The base bitumen is preheated to 150–160 °C; YH-898 pellets are added gradually, and the mixture is brought to 180–190 °C under high-shear agitation. Rotor-stator gap shear rates above 10,000 s−1 are required to reduce SBS-rich domains to a fine, stable morphology. Under low-shear agitation, the polymer phase coalesces, and the modified binder shows storage separation and reduced elastic recovery. Performance is assessed by penetration per ASTM D5, softening point per ASTM D36, elastic recovery per ASTM D6084, and storage stability per ASTM D7173. At 5 wt% YH-898, the softening-point gain over unmodified bitumen is commonly in the range of 10–25 °C; the gain is lower than that obtained with a 40 wt% styrene SBS, but low-temperature cracking resistance is typically better. Above 6 wt% polymer, modified binder tanks require recirculation loops to control top-phase enrichment because the density difference between SBS and bitumen is insufficient to prevent creaming at rest. Dispersion below 160 °C is ineffective because the polymer chains lack sufficient mobility, while processing above 200 °C accelerates polybutadiene degradation and produces a rapid loss of elastic recovery after short-term aging. The use of sulfur or peroxides for crosslinking in SBS-modified bitumen is not part of the normal physical modification route for YH-898; if crosslinking is attempted, the dosage must be controlled below the point of gelation and verified by dynamic shear rheometry per ASTM D7175.

    Impact modification of polypropylene and polyethylene with YH-898 is performed on a co-rotating twin-screw extruder with an L/D ratio of 40:1 and vacuum devolatilisation. The polyolefin is metered at the main feed throat and melted at 170–190 °C; YH-898 pellets are side-fed downstream at 5–15 wt% to limit peak torque and prevent block copolymer aggregation. Barrel temperatures are zoned from 170 °C at the feed section to 210 °C at the die, while melt temperature is held below 220 °C. Notched Izod impact at 23 °C per ASTM D256 improves as SBS loading increases, but low-temperature impact improvement is smaller than that achieved with SEBS at equal loading. The glass transition temperature of the polybutadiene midblock is below −70 °C; however, oxidative embrittlement during hot-air aging at 100 °C must be controlled with a secondary thiosynergist and hindered phenolic antioxidant. Weld-line strength is a key process limitation: parts with long flow paths can show weakness at knit lines, and published data for YH-898 specifically in thin-wall injection-moulded packaging is limited. Production trials should therefore include weld-line impact specimens cut from the actual part.

    Solvent-borne adhesive processing is also used where low application temperature is required. YH-898 dissolves in toluene or cyclohexane to 20–25 wt% solids at 25 °C under low-shear agitation; solution viscosity is measured with a Brookfield viscometer per ASTM D2196. Coated films are dried at 70–90 °C with solvent recovery. The butadiene block is shear-sensitive in solution, so high-speed dissolver blades should be operated below 1,000 rpm for extended mixing to avoid chain scission and loss of room-temperature cohesion. Solution viscosity is strongly shear-thinning; coating equipment should be calibrated with the actual solvent balance because toluene retention above 0.5 wt% can depress peel adhesion and raise blocking in roll form.

    Incoming quality control for YH-898 typically includes melt mass-flow rate, volatile matter, and ash. Lot-to-lot variation within the 0.1–5.0 g/10 min MFR band can shift feeding behaviour on gravimetric extrusion lines. On a 75 mm co-rotating twin-screw extruder with a 40:1 L/D and strand pelletising head, pellet lots at the lower MFR limit may require screw-speed increases of up to 25% to maintain a constant melt temperature profile; this adjustment is process-specific and should be confirmed by torque and barrel-pressure monitoring. The product is not hygroscopic in the polyester or polyamide sense, but porous pellet morphology increases exposed surface area and makes surface moisture a greater concern than bulk moisture. Silo storage with dry-air purge at 0.5–1.0 m³/min per tonne is sufficient in most warehouses.

    Regulatory status is defined by the formulated article, not by the neat SBS

    Neat SBS YH-898 is a synthetic polymer; as such it is generally exempt from European Union REACH registration under Article 2(9) and Article 3(5) of Regulation (EC) No 1907/2006, although its constituent monomers, styrene and butadiene, are registered when required. The raw polymer is not a formulation under the RoHS Directive 2011/65/EU; compliance must be demonstrated on the final electrical or electronic article for lead, mercury, cadmium, hexavalent chromium, and restricted brominated flame retardants listed in Annex II. Food-contact use of YH-898 can only be considered when the compound complies with the appropriate national or regional standard, such as FDA 21 CFR 177.1810 or European Union Regulation (EU) No 10/2011, and migration testing has been completed on the final package. The unsaturated polybutadiene block limits use in hot-air environments above 80 °C for long service life unless stabilisers are added. Avoid storage in direct ultraviolet light and avoid contact with strong oxidisers, copper-based heat stabilisers, and amine-based additives that may promote discolouration in certain adhesive formulations. These restrictions are operational rather than regulatory, but they define the practical envelope for YH-898 in industrial use.

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