SINOPEC Baling Hunan SBS YH-805
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Product Name:
SINOPEC Baling Hunan SBS YH-805
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Factroy Site:
Yudu County, Ganzhou, Jiangxi, China
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Price Inquiry:
sales8@ascent-chem.com
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Manufacturer:
Ascent Petrochem Holdings Co., Limited
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CONTACT NOW
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SINOPEC Baling Hunan SBS YH-805 is typically used in formulations when styrene content and melt flow rate must be controlled within specific ranges.
Specifications
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HS Code
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896606
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| Appearance |
White or light-yellow porous pellets |
| Product Type |
Styrene-butadiene-styrene block copolymer thermoplastic elastomer |
| Block Structure |
Linear |
| Styrene Content |
Approximately 30% |
| Volatile Matter |
≤0.7% |
| Ash Content |
≤0.2% |
| Tensile Strength |
≥15.0 MPa |
| Elongation At Break |
≥700% |
| 300 Modulus |
≥2.0 MPa |
| Permanent Set |
≤30% |
| Shore A Hardness |
75 ± 5 |
| Density |
0.94 g/cm³ |
| Melt Flow Rate |
1.0–5.0 g/10 min |
As an accredited SINOPEC Baling Hunan SBS YH-805 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-805 is supplied in 25 kg moisture-proof woven bags with inner liners for storage and transport. |
| Container Loading (20′ FCL) |
20′ FCL loaded with SINOPEC Baling Hunan SBS YH-805 in bags/pallets, securely stowed and sea-fastened for export shipment. |
| Shipping |
SINOPEC Baling Hunan SBS YH-805 is shipped as a non-hazardous thermoplastic elastomer in moisture-proof bags or cartons. Store and transport in a cool, dry, ventilated area, away from direct sunlight, heat, and moisture; avoid packaging damage and contamination. |
| Storage |
Store SINOPEC Baling Hunan SBS YH-805 in a cool, dry, well-ventilated warehouse, away from direct sunlight, heat, moisture, sparks, and open flames. Keep original packaging sealed and undamaged; avoid contamination, excessive stacking, and prolonged UV/ozone exposure. Use first-in, first-out rotation and handle gently to prevent crushing or deformation. |
| Shelf Life |
SINOPEC Baling Hunan SBS YH-805 has a 12-month shelf life when stored dry and cool in original packaging, away from sunlight. |
Application of SINOPEC Baling Hunan SBS YH-805
Terminal blending of SINOPEC Baling Hunan SBS YH-805 into penetration-grade paving bitumen typically begins with a pre-swelling phase in which the linear triblock architecture absorbs maltene-phase oils at a temperature between 170 °C and 185 °C. The practical target for dense-graded highway wearing courses lies between 3.5 wt% and 5.5 wt% of the neat bitumen mass; for stone-mastic asphalt and open-graded friction course binders, the loading shifts to 5.5–7.0 wt% because the higher film thickness and drainage-prone aggregate skeleton demand greater elastomeric recovery. In terminal blending operations, the base bitumen is preheated to 175–180 °C and transferred to a vertical rotor-stator mill operating at 1,500–3,000 rpm; the polymer is metered through a screw feeder at a rate matched to a binder throughput between 50 t/h and 150 t/h. After milling, the binder matures in agitated tanks for 2–4 h at 175–185 °C, during which time the styrene domains associate into physical crosslinks that produce the elastic recovery measured under ASTM D6084-21. Storage tanks must be blanketed with nitrogen or other inert gas because prolonged exposure of the butadiene midblock to oxygen at temperatures above 180 °C promotes chain scission and gel formation, which appears as a rising softening point and a loss of ductility.Compliance for polymer-modified bitumen is assessed through AASHTO M 320-23 Table 1 performance grades, ASTM D5976-96 for Type I SBS-modified binders, and EN 14023:2010 for European polymer-modified paving binders. Elastic recovery according to ASTM D6084-21 should generally exceed 70% at 25 °C for SBS-modified grades; viscosity at 135 °C is controlled under ASTM D4402-15 to remain below 3 Pa·s to satisfy pumpability requirements at hot-mix plants. Storage stability is determined by ASTM D7173-20, with a softening-point difference of no more than 2.5 °C between the top and bottom of a conditioned tube after 48 h at 163 °C. A difference above 2.5 °C indicates inadequate dispersion or excessive diblock content and requires re-milling or the use of a compatibilizing aromatic flux oil.Downstream, the modified binder is transferred to a drum mix plant or batch plant where it is blended with aggregate at 160–170 °C. In dense-graded mixes, the binder content is typically 4.8–5.6 wt% of total mix; in SMA and OGFC, the binder content may be 5.8–6.5 wt% because of the void structure. Production-grade equipment includes counter-flow drum mixers with reclaimed asphalt pavement collar stations and storage silos maintained below 170 °C to limit oxidative ageing. End-product types include PG 70-22 and PG 76-22 dense-graded wearing course, SMA surface course, OGFC overlays, and stress-absorbing membrane interlayers. The limiting operational condition is temperature: prolonged storage above 195 °C accelerates gel particle formation, while discharge below 160 °C increases viscosity enough to reduce aggregate coating consistency on the drum flight.
Why Does YH-805 Loading in Torch-Applied Bituminous Membrane Compound Peak at 12 wt%?
At loadings above 12 wt% of the bitumen phase in a torch-applied roofing membrane, the Brookfield Thermosel viscosity at 150 °C rises into a range that reduces three-roll calender throughput and makes the compound difficult to transfer through jacketed pipework without raising temperature above 180 °C. The practical loading window for YH-805 in waterproofing compounds is 8–12 wt% of the bitumen fraction, with the lower end used for self-adhesive membrane compounds that must retain low-temperature cold bending and the upper end used for torch-applied sheets that require high dimensional stability under roof fire exposure. A representative formulation includes 8–12 wt% YH-805, 20–35 wt% limestone filler, 3–6 wt% process oil, and 0.1–0.3 wt% antioxidant based on the total compound; the compound is produced in a horizontal plough mixer or a heated high-viscosity disperser with a jacket temperature between 160 °C and 170 °C. Mixing continues for 45–90 min after polymer addition, with the filler introduced in two portions to prevent torque spikes and localized overheating on the vessel wall.Compliance for these sheets is anchored to EN 13707:2004+A2:2009 for flexible sheets for waterproofing and ASTM D6164-19 for SBS polymer-modified bituminous sheet materials. Low-temperature flexibility is evaluated under EN 1109:2013 at -20 °C for torch-applied grades; the sheet is conditioned for 2 h before bending over a mandrel of specified radius without cracking. Softening point of the bitumen compound is measured by ASTM D36-14 and typically falls between 115 °C and 135 °C for the upper loading range.Downstream production converts the compound into membrane on a calender or slot-coating line. The molten compound at 150–165 °C is applied to a 140–180 g/m² polyester carrier at a thickness of 3–5 mm, then surfaced with sand, slate granules, or a peelable film. Line speed is governed by cooling capacity; the sheet must be cooled below 45 °C before winding to avoid blocking and deformation. End-product types include torch-applied polyester-reinforced SBS membranes, self-adhesive cold-applied sheets, and underlayments for mechanically fastened roof systems. The primary incompatibility is with solvent-based primers and cutback bitumens containing high aromatic oils; direct contact with these solvents attacks the butadiene-rich domains and can reduce tensile strength at 23 °C below the minimum specified in ASTM D6164-19.Injection-Molding Parameters for YH-805-Expanded Footwear Skin and Unit Sole Compounds
Industrial sole compounds based on YH-805 are customarily pre-melted in a co-rotating twin-screw extruder with a length-to-diameter ratio between 36:1 and 44:1, with barrel temperatures set in the range 150–170 °C for feeding and melting and the die temperature held at 160–170 °C. The compound formulation is built from 35–50 phr YH-805, 10–25 phr paraffinic or naphthenic oil, 5–15 phr general-purpose polystyrene to raise hardness, 10–20 phr precipitated silica or calcium carbonate filler, and 0.2–0.5 phr antioxidant. High-shear dispersion of the filler at the upstream barrel section is necessary to avoid aesthetic defects in the finished sole; unmelted filler agglomerates appear as surface pitting after injection. Strand pelletizing after a two-hole die and water-bath cooling at 20–35 °C yields pellets that are dried to a moisture content below 0.05 wt% before injection molding because residual moisture above this threshold produces splay and internal voids.Injection molding of YH-805-based footwear components is performed on reciprocating-screw machines with clamp force between 80 t and 120 t for multi-cavity sole molds. Melt temperature at the nozzle is maintained at 170–190 °C; barrel temperatures are often set in a flat profile to minimize thermal gradient. Mold temperature is controlled at 25–45 °C, and injection pressure is set between 40 MPa and 70 MPa, with holding pressure typically 30–50% of peak injection value and holding time adjusted to gate freeze. The higher styrene content of YH-805 supplies rapid solidification and good mold release, but long residence times above 15 min at 190 °C can cause gate blush and slight yellowing. Compliance requirements for footwear elastomers include ASTM D2240-15 for Shore A hardness, ASTM D638-14 for tensile strength and elongation, and ISO 5423:2023 for moulded plastics footwear terms and test methods; European shipments must conform to REACH Annex XVII restrictions that cover PAH content in consumer footwear elastomers.End-product types include direct-injected casual shoe outsoles, sandal and slipper unit soles, sheet soling, and lightweight foam-molded midsoles where a chemical blowing agent is added at 0.5–1.5 phr. In direct-injection constructions, the sole compound is injected onto a primed textile or leather upper at the same melt temperature window; bond strength depends on the preheat of the upper below 60 °C and on the use of a chloroprene-based primer. Failure modes observed on production lines include edge tearing when the mold temperature is below 25 °C, and surface tack when the mold temperature exceeds 45 °C and cooling time is insufficient.A hot-melt pressure-sensitive adhesive formulation containing YH-805 at 22–28 wt% of the total compound becomes pumpable only after the styrenic end blocks have been solvated by a compatible tackifier resin while the butadiene midblock remains partly phase-separated to preserve cohesive shear. The compound is prepared in a sigma-blade mixer with a jacket temperature of 150–170 °C under a nitrogen blanket at 0.2–0.5 bar positive pressure; the order of addition typically places the SBS pellets into preheated tackifier and oil at 140–150 °C before the melt is raised to 160–170 °C for the final 20–40 min of mixing. A representative hot-melt PSA formula contains 20–30 wt% YH-805, 40–55 wt% C5 aliphatic or partially hydrogenated rosin ester tackifier, 15–25 wt% naphthenic process oil, and 0.5–1.0 wt% phenolic or phosphite antioxidant; the high diblock content of YH-805 lowers mix viscosity during application but must be balanced against shear resistance in the coated film.Coating is performed on slot-die or roll-coating lines at an application temperature of 140–160 °C, with coat weight controlled between 18 g/m² and 30 g/m² on biaxially oriented polypropylene or polyester substrate. Line speed is typically 150–300 m/min for tape and label stock, with the adhesive layer cooled below 30 °C before winding to avoid blocking. Compliance for food-contact tapes and indirect food labels is governed by FDA 21 CFR 175.105 for adhesives and 21 CFR 177.2600 for rubber articles intended for repeated contact; for EU shipments, the formulation must be screened under REACH Annex XVII and relevant food-contact migration limits. Shear adhesion failure temperature is measured by ASTM D4498-07 with a 500 g static load and a heating rate of 0.5 °C/min; loop tack is evaluated under ASTM D6195-03 and 180° peel under ASTM D3330/D3330M-04.End-product types include carton-sealing tapes, general-purpose label stock, hygiene construction adhesives for disposable nonwovens, and transfer tapes for automotive interior bonding. The primary processing limitation is viscosity stability at 150 °C: formulations with more than 35 wt% highly aromatic tackifier can plasticize the styrene domains, lower the SAFT below 70 °C, and produce edge ooze during coated roll storage. Published data for this specific configuration is limited for all tackifier combinations, so pilot coating trials on a 120 mm slot-die head are recommended before specifying a full commercial run.When Polypropylene Homo-Polymer Requires Low-Temperature Notch Toughness Without Beta-Nucleation
The incorporation of YH-805 into polypropylene homopolymer at 5–15 wt% is performed on a co-rotating twin-screw line with an L/D of 40:1 and barrel temperatures between 180 °C and 220 °C. YH-805 is pre-blended with the PP pellets in a low-speed tumble mixer at 0.5 wt% mineral oil to prevent segregation, then fed into the main hopper; the screw profile uses a combination of right- and left-handed kneading blocks to distribute the SBS phase without inducing excessive viscous heating beyond 230 °C. The compounded pellets are used in injection molding at a melt temperature of 200–220 °C and a mold temperature of 40–60 °C. At 10 wt% SBS loading, notched impact toughness at -20 °C is often assessed under ISO 180:2023 or ASTM D256-23; the addition moves the failure mode from brittle to ductile in thin-wall sections but reduces tensile yield stress measured by ISO 527-2:2012 because the butadiene midblock contributes no crystallinity.Compliance for these modified PP compounds falls under ISO 180:2023, ISO 527-2:2012, ASTM D256-23, and European REACH substance registration. The addition ratio is constrained at the upper end by stiffness loss and at the lower end by insufficient low-temperature impact: below 5 wt%, the particle spacing is too large to stabilize crazing ahead of a propagating notch; above 15 wt%, tensile modulus declines enough to affect snap-fit designs in appliance housings. Published data for this specific configuration is limited, and processors should verify the notched impact and modulus balance on the production tool rather than relying solely on laboratory plaques.Downstream processes include pellet compounding, injection molding, and occasionally extrusion-thermoforming of sheet for interior trim. The end-product types are refrigerator interior panels, washing machine outer tubs, automotive interior close-out panels, and battery tray edges for low-speed electric vehicles. A specific incompatibility is the use of peroxide masterbatch in the same feeding system: peroxide radicals attack the unsaturated butadiene midblock and cause viscosity reduction and impact loss, so the feed hopper and screw must be purged after peroxide runs with a virgin PP purge compound before YH-805 re-introduction.Replacement of 10–25 phr natural rubber or SBR with YH-805 in a sulphur-cured mechanical goods compound changes the cure trace recorded on a moving-die rheometer: the linear SBS introduces butadiene unsaturation that participates in accelerated sulphur crosslinking, while the styrene end blocks prolong scorch time and increase compound modulus after cure. The compound is prepared in an internal mixer with a chamber temperature of 60–70 °C for the masterbatch stage, then the sulphur and accelerator are added on a two-roll mill at 50–60 °C to avoid premature vulcanization. A representative compound might contain 100 phr total elastomer in which YH-805 accounts for 10–25 phr, carbon black 40–70 phr, naphthenic oil 5–15 phr, zinc oxide 3–5 phr, stearic acid 1–2 phr, sulphur 1.5–2.5 phr, and sulphenamide accelerator 1.0–1.5 phr.Curing is performed in a compression mould at 150–160 °C for a time equivalent to t90 plus 2–3 min, as determined by ISO 6502-3:2023 or ASTM D5289-19. Mechanical properties after cure are measured under ISO 37:2017 for tensile stress-strain and ASTM D412-16 for the equivalent North American method; hardness is determined with ASTM D2240-15. Compliance for industrial goods that contact food in repeated use may require FDA 21 CFR 177.2600; products for consumer use in the EU must comply with REACH Annex XVII and specific migration limits when applicable.End-product types include industrial floor mats, anti-vibration pads for compressor feet, sheet soling for stitched footwear, and rubber buffer blocks for loading docks. The main processing limitation is the incompatibility of the styrene block with high levels of paraffinic process oil: oil above 20 phr selectively plasticizes the styrene domains and reduces tear strength measured by ISO 34-1:2022. The mill temperature must not exceed 70 °C during the addition of YH-805 because the butadiene midblock begins to soften and stick, causing banding loss on the front roll and uneven accelerator dispersion.
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Certification & Compliance
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SINOPEC Baling Hunan SBS YH-805 is manufactured under an ISO 9001 quality system and complies with relevant regulatory requirements.
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COA, SDS/MSDS, and related certificates are available upon request.
For certificate requests or inquiries, contact: sales8@ascent-chem.com.
More Introduction
SINOPEC Baling Hunan SBS YH-805 is a linear styrene-butadiene-styrene block copolymer produced by anionic polymerization at Baling Petrochemical, Hunan. The grade is specified for asphalt modification, hot-melt and solvent-borne adhesive compounding, footwear sole formulations, and polymer modification where the balance of styrene endblock content and butadiene midblock structure controls compatibility with aromatic process oils, aliphatic tackifiers, and filler systems. The product is supplied as a porous pellet or crumb; the porous pellet form is preferred in solvent-dissolution operations because of shorter dissolution time in toluene/ethyl acetate blends. In bitumen modification, YH-805 is incorporated at 2–6 mass% by high-shear mixing. In pressure-sensitive adhesives, the polymer is compounded at 20–30 mass% solids. In footwear formulations, the grade functions as the elastomeric base after oil extension and filler addition. The model designation identifies a linear SBS with an intermediate styrene mass fraction and melt processability positioned between lower-styrene and higher-styrene Baling grades.
The following table compiles representative property windows reported for YH-805-class linear SBS. Actual certificate-of-analysis limits may differ by production campaign and should be confirmed against the current technical datasheet before formulating.
| Property | Typical range | Test method |
| Styrene mass fraction | 30–40 mass% | Producer internal method; confirm with TDS |
| Tensile strength | 18–24 MPa | ASTM D638-14 |
| Elongation at break | 550–700% | ASTM D638-14 |
| 300% modulus | 2.0–3.0 MPa | ASTM D638-14 |
| Shore A hardness | 75–88 | ISO 868:2003 |
| Melt flow rate, 200 °C/5 kg | 2–10 g/10 min | ISO 1133-1:2022 |
| Volatile matter | ≤1.0 mass% | ASTM D5668 |
| Ash | ≤0.2 mass% | ISO 247-1 |
What distinguishes YH-805 from YH-792 and YH-796 in bitumen modification?
The primary differentiation is styrene mass fraction and melt viscosity. YH-792 is generally specified with a styrene mass fraction near 40 mass%, which gives high tensile strength and hardness but slower dissolution and higher melt viscosity. YH-796 carries a lower styrene mass fraction near 20–25 mass%, providing greater low-temperature flexibility and faster dissolution but lower cohesive strength. YH-805 occupies an intermediate position with reported styrene mass fractions in the 30–40 mass% range. This shifts the order-disorder transition temperature and the glass transition of the styrene domains accordingly. In bitumen, higher styrene block content increases the viscosity plateau after high-shear dispersion and reduces low-temperature cracking resistance if the binder is not formulated with extender oil. The linear architecture of YH-805 yields shear-thinning behavior at lower shear rates than radial grades, but melt strength is lower than that of star-shaped SBS grades. Published data for this specific configuration is limited; formulators should confirm single-lot tensile and melt flow rate values against the current technical datasheet.
Bitumen modification with YH-805 is carried out in heated vessels equipped with rotor-stator high-shear mixers. The binder is preheated to 160–170 °C, and polymer is added at 2–6 mass% of bitumen. High-shear mixing at 170–190 °C for 45–120 min is required to disperse the polymer into particles below 10 µm; incomplete dispersion leaves domains above 50 µm that do not contribute to the elastomeric network and may re-agglomerate during storage. The processing window is bounded at the lower end by the melt viscosity of the styrene block domains. Below 160 °C, the styrene domains remain largely glassy, increasing torque and reducing dispersion efficiency. The upper bound is controlled by thermo-oxidative degradation of the butadiene midblock. Above 200 °C, chain scission and crosslinking compete, and viscosity drift can exceed 15% within 60 min. Production-scale field reports describe gel formation and viscosity drift in tanks where nitrogen blanketing is absent and residence time at 190 °C exceeds 120 min. Rotor-stator tip speeds of 15–25 m/s are commonly used in industrial practice, but published data for this specific configuration is limited.
Thermo-oxidative degradation imposes a narrow barrel-temperature envelope in hot-melt compounding
Processing of YH-805 in hot-melt adhesives is performed in twin-screw extruders with L/D ratios of 40:1 to 52:1. Barrel temperatures are set between 150 °C and 180 °C, with the feed zone maintained below 100 °C to avoid pellet agglomeration. Screw speeds of 200–400 min⁻¹ generate shear heating; melt temperatures measured at the die should not exceed 190 °C. The material is hygroscopic in high-humidity storage. Pre-drying at 60–70 °C for 2–4 h is required when storage RH exceeds 60%. Failure to predry results in surface voids and reduced peel adhesion in slot-die coating. Antioxidant packages based on hindered phenols and phosphites are standard. Amine-based antidegradants should be avoided because interaction with residual coupling agents can produce color bodies and gel particles. The melt flow rate determined according to ISO 1133-1:2022 at 200 °C/5 kg is typically in the 2–10 g/10 min range. Lower values are associated with high-molecular-weight lots that require higher extrusion temperatures but give higher cohesive strength.
The following table summarizes reported application differentiation among Baling linear SBS grades. The values are approximate and should be confirmed against the producer’s release documents.
| Grade | Styrene mass fraction range | Melt flow behavior | Primary application differentiation |
| YH-792 | 40 mass% | Lower MFR, higher melt viscosity | High tensile strength; asphalt and shoe soles |
| YH-796 | 20–25 mass% | Higher MFR, faster dissolution | Low-temperature flexibility; adhesives |
| YH-805 | 30–40 mass% | Intermediate MFR | Balanced cohesive strength and processability |
When solvent blends shift from aromatic to aliphatic, viscosity response changes abruptly
Dissolution of YH-805 in toluene/ethyl acetate/aliphatic hydrocarbon blends produces adhesives whose viscosity depends on styrene domain solvation and molecular weight. In toluene-rich blends, the styrene endblocks are solvated, and the solution behaves as a viscoelastic fluid. In aliphatic-rich blends, only the butadiene midblock is solvated, and the styrene domains remain associated, producing higher low-shear viscosity and yield stress. A typical starting formulation contains 20–30 mass% YH-805, 40–60 mass% aromatic tackifier, and the balance solvent. Viscosity measured on a Brookfield RVT at 20 °C may range from 500 mPa·s to 5,000 mPa·s depending on solvent composition. The styrene endblock content gives a glass transition near 95 °C for the styrene domains, while the butadiene midblock glass transition is below -80 °C. This phase-separated morphology is responsible for pressure-sensitive tack and shear resistance. The addition of hydrocarbon tackifier at 1:1 polymer-to-tackifier ratio lowers the plateau modulus and shifts the tack window toward room temperature. Coating weight uniformity requires viscosity stability; lot-to-lot variation in diblock content below 1 mass% is generally acceptable, while higher diblock content reduces shear holding power measured according to PSTC-107.
Oil extension and silica filler loading in footwear sole formulations
In footwear sole formulations, YH-805 is typically oil-extended with naphthenic or paraffinic process oil at 5–30 phr and compounded with silica filler at 10–40 phr. The combination of oil and filler reduces Shore A hardness from the neat polymer value of 75–88 to 55–70, depending on filler surface area and silane coupling agent. Mixing in an internal mixer with a fill factor of 0.75–0.85 and dump temperatures of 110–130 °C is standard. When silica loading exceeds 40 phr, compound Mooney viscosity increases sharply, and injection molding requires clamp force settings above 150 t for multi-cavity molds. Lower clamp force may result in flash and incomplete cavity filling. Abrasion resistance measured according to DIN 53516 is influenced more by filler dispersion than by SBS grade; undispersed silica agglomerates larger than 10 µm initiate wear. YH-805 differs from YH-792 in footwear applications by offering lower melt viscosity at a given styrene content, which improves flow in thin-section soles but reduces green strength. Published data for this specific configuration is limited, and laboratory compounding is required before production scale-up.
Regulatory documentation for YH-805 includes REACH and RoHS compliance statements. If food contact is required, FDA 21 CFR 177.1810 is not automatically applicable and must be confirmed for the specific finished article. Storage should be in dry conditions below 40 °C. The product contains unsaturated butadiene units that are subject to oxidation; inventory should be used within 12 months. Avoid prolonged exposure to strong oxidizing agents and copper-containing alloys because copper ions catalyze butadiene oxidation. For asphalt modification, avoid combination with amine-based adhesion promoters in the same high-shear vessel without validation; amine compounds can accelerate gel formation in SBS-modified bitumen. The product is incompatible with high-aromatic process oils at very high loading because excessive solvation of the styrene domains reduces tensile strength and heat resistance.