Products

Ningbo Changhong SBS CH1401HE

    • Product Name: Ningbo Changhong SBS CH1401HE
    • Factroy Site: Yinchuan, Ningxia, China
    • Price Inquiry: sales8@ascent-chem.com
    • Manufacturer: Ascent Petrochem Holdings Co., Limited
    • CONTACT NOW
    VTB
    Specifications
    HS Code 483303
    Manufacturer Ningbo Changhong Polymer Scientific & Technical Co., Ltd.
    Product Name Ningbo Changhong SBS CH1401HE
    Material Type Styrene-butadiene-styrene block copolymer (SBS)
    Grade CH1401HE
    Appearance White or light-yellow porous pellets
    Styrene Content 40% typical
    Butadiene Content 60% typical
    Density 0.94-0.95 g/cm³ typical
    Shore A Hardness 85 typical
    Tensile Strength ≥16 MPa typical
    Elongation At Break ≥700% typical
    Permanent Set ≤30% typical
    Volatile Matter ≤0.5%
    Ash Content ≤0.2%
    Melt Flow Rate 0.5-2.0 g/10 min typical

    As an accredited Ningbo Changhong SBS CH1401HE factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Ningbo Changhong SBS CH1401HE packaging: 25 kg PE-lined woven bags, palletized for industrial storage and transport.
    Container Loading (20′ FCL) A 20-foot FCL container is loaded with Ningbo Changhong SBS CH1401HE chemical, securely packed and stowed for shipment.
    Shipping Ningbo Changhong SBS CH1401HE is a non-hazardous styrene-butadiene-styrene block copolymer supplied as solid granules/pellets in 25 kg bags, palletized and shipped in dry containers at ambient temperature. Not regulated for transport; keep cool, dry, and protected from moisture, heat, and direct sunlight.
    Storage Store in a cool, dry, well-ventilated warehouse away from direct sunlight, heat, flames, sparks, and strong oxidizers. Keep in original sealed bags or containers, palletized and off the floor, protected from moisture and contamination. Avoid dust generation and static buildup; use stable stacking, FIFO rotation, and comply with local regulations.
    Shelf Life Shelf life is typically 12 months when stored in a cool, dry, well-ventilated area, away from direct sunlight and moisture.
    Application of Ningbo Changhong SBS CH1401HE

    During high-shear compounding of hot-melt pressure-sensitive adhesive systems, CH1401HE is introduced at 15–25 wt% of the total adhesive mass, with the balance split between a hydrogenated C5 or C9 tackifier at 45–55 wt%, naphthenic process oil at 20–30 wt%, and a hindered phenolic/phosphite antioxidant package at 0.5–1.0 phr. Processing is carried out in a jacketed sigma-blade kneader or twin-screw extruder with L/D 30:1 and a barrel temperature profile from 140°C to 170°C; the tackifier is pre-melted and added to the rubber phase before oil injection to avoid phase inversion and viscosity instability. Subsequent hot-melt coating applies at 150–165°C through a slot-die onto release liner; viscosity measured by Brookfield RVT Thermosel spindle 27 at 160°C is maintained at 4,000–15,000 mPa·s for stable coating. Compliance path uses PSTC-101 Method A 180° peel adhesion, ASTM D6195-03(2019) loop tack, ASTM D3654/D3654M-06 shear adhesion, and FDA 21 CFR 175.105 for indirect food-contact tapes; terminal products include single-coated carton sealing tapes, labelstock, protective film, and diaper landing zone tapes.

    What Limits SBS Loading in Bituminous Waterproofing Membrane Compounds?

    Bituminous membrane formulations introduce CH1401HE at 5–8 wt% of the finished bituminous binder for torch-applied membranes and 8–12 wt% for self-adhesive cold-applied membranes, dispersed into paving-grade or oxidised bitumen at 170–190°C using a high-shear rotor-stator mill; dispersion time of 45–90 min depends on bitumen aromaticity and mill tip speed above 15 m/s. Higher styrene block cohesion of a linear SBS grade preserves elevated-temperature resistance, but loading beyond 12 wt% is constrained by viscosity exceeding 3,000 mPa·s at 180°C and phase gelation during storage. Ring-and-ball softening point per ASTM D36 rises into the 110–130°C range at 6–8 wt% SBS, while penetration per ASTM D5 drops to 30–50 dmm; low-temperature flexibility per EN 1109 reaches -15°C to -25°C. Production-line equipment includes vertical high-speed dispersers with bitumen preheated in indirect thermal oil jackets and nitrogen purge to reduce oxidative skin formation. Compliance is established through EN 13707 for reinforced bituminous waterproofing sheets, ASTM D6164/D6164M-21 for polyester-reinforced modified bitumen membranes, and EN 13969 for damp-proof courses; terminal products include torch-applied roofing membranes, bridge deck waterproofing sheets, foundation tanking membranes, and self-adhesive repair flashings.

    Solvent-Borne Contact Adhesives Demand Stabilized Viscosity More Than High Peak Strength

    For solvent-borne contact adhesive production, CH1401HE is dissolved at 15–25% solids in a toluene/cyclohexane/methyl ethyl ketone blend, with SBS addition ratios of 10–15 wt% of the wet formulation and tackifying resin at 50–70 phr of rubber; a plasticizer such as 2,2,4-trimethyl-1,3-pentanediol diisobutyrate may be used at 5–10 phr to extend open time. Mixing is conducted in a closed stainless-steel high-speed disperser at 700–1,200 rpm for 60–120 min, with cooling jacket held below 40°C to limit solvent evaporation; final viscosity is adjusted to 1,000–3,000 mPa·s for brush and roller application. Green-strength development is assessed by ASTM D903-98(2017) 180° peel on canvas-to-rubber specimens after 2 min and 24 h, while heat resistance is determined by dead-load shear at 60°C per ASTM D816-06. Regulatory compliance includes GB 33372-2020 VOC limits for adhesives, REACH SVHC screening, and ASTM D4236 for chronic health labelling in consumer shoe repair kits; terminal products include footwear upper-to-sole lamination, furniture edge-banding, automotive headliner bonding, and construction panel contact adhesives.

    Application scenarioPrimary compliance standardCritical test methodCH1401HE addition ratio
    Hot-melt pressure-sensitive adhesiveFDA 21 CFR 175.105; PSTC-101ASTM D3654/D3654M-06; Brookfield RVT Thermosel at 160°C15–25 wt%
    Bituminous waterproofing membraneEN 13707; ASTM D6164/D6164M-21ASTM D36; ASTM D5; EN 11095–12 wt%
    Solvent-borne contact adhesiveGB 33372-2020; ASTM D4236ASTM D903-98(2017); ASTM D816-0610–15 wt%
    Injection-moulded sole compoundREACH Annex XVII Entry 50; ISO 2781:2018ASTM D2240; ASTM D412; DIN 5351650–70 phr
    Impact-modified polypropyleneFDA 21 CFR 177.1520; ISO 180:2023ISO 527-2:2012; ASTM D256-235–15 wt%
    Hot-applied bituminous joint sealantASTM D3406-17; ASTM D5329ASTM D1190; vacuum kettle moisture removal10–20 wt%

    Injection-moulded sole compounds built on CH1401HE are blended at 50–70 phr with general-purpose polystyrene at 30–50 phr, naphthenic oil at 10–20 phr, calcium carbonate or silica filler at 20–40 phr, and a hindered phenolic antioxidant at 0.5–1.0 phr. The first stage is a counter-rotating twin-screw extruder with L/D 30:1 and barrel temperatures of 140–180°C; the second stage is an injection-moulding machine with barrel profile 160–190°C, mould temperature 25–40°C, and clamp force scaled to projected area at 60–100 MPa injection pressure. Hardness is controlled to Shore A 55–65 per ASTM D2240, tensile strength above 8 MPa per ASTM D412, and DIN 53516 abrasion volume below 250 mm³; flex-cracking resistance is screened by ASTM D1052 Ross flex cut growth at 100,000 cycles. The processing boundary for CH1401HE is defined by butadiene midblock thermo-oxidative degradation above 190°C and pellet block agglomeration during storage above 40°C; facilities with unheated warehouses should specify a 24 h conditioning step at 23±2°C before hopper loading. Compliance references include REACH Annex XVII Entry 50 for PAH limits in footwear and ISO 2781:2018 for density determination; terminal products are injection-moulded sandal soles, unit soles, sports-shoe midsoles, and low-profile fashion soles.

    Thermoplastic Modifier Dispersion in Impact-Modified Polypropylene

    To modify polypropylene impact toughness, CH1401HE is melt-compounded into polypropylene homopolymer or impact copolymer at 5–15 wt% using a co-rotating twin-screw extruder with L/D 40:1, temperature profile 180–230°C, and screw speed 300–600 rpm; the SBS pellets are fed through the main throat while mineral fillers, if present, enter at a downstream side feeder to limit filler attrition. Notched Izod impact strength per ISO 180/A is improved from the unfilled PP baseline, but the unsaturated butadiene midblock reduces long-term heat-aging and UV stability, restricting use to interior or dark-coloured components unless UV stabilizers are added at 0.5–1.5 wt%. Tensile modulus per ISO 527-2 decreases with each 1 wt% SBS addition, so load-bearing structural parts should not exceed 10 wt%. Melt processing uses a melt-filtration screen pack of 40/60/80 mesh and underwater pelletizing with water temperature 15–25°C; pre-drying of CH1401HE is required only when packaging has been opened above 60% RH for more than 24 h. Compliance is anchored by ASTM D256-23 for impact resistance, ISO 180:2023 for notched impact, ISO 527-2:2012 for tensile properties, and FDA 21 CFR 177.1520 for PP food-contact components in non-fatty dry food service; terminal products include appliance housing ribs, automotive interior trim, extruded edge profiles, and reusable crates.

    When CH1401HE is evaluated for hot-applied bituminous joint sealants, the formulation ratio is 10–20 wt% of the total compound, with oxidised bitumen at 60–75 wt%, ground tyre rubber or mineral filler at 10–20 wt%, and synthetic wax at 1–3 wt%; the compound is mixed in an agitated vacuum kettle at 160–180°C under -0.08 MPa vacuum to remove moisture and air, then transferred to heated application units; specifications for paving joint sealants reference ASTM D3406-17 for hot-applied elastomeric-type joint sealant and ASTM D5329 for adhesion-in-tension testing, while terminal products include highway expansion-joint sealants, roofing repair mastics, bridge deck crack sealers, and anti-corrosion tank-base mastics.

    Free Quote

    Competitive Ningbo Changhong SBS CH1401HE prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please contact us at +8618005193850 or mail to sales8@ascent-chem.com.

    We will respond to you as soon as possible.

    Tel: +8618005193850

    Email: sales8@ascent-chem.com

    Inquiry

    Get Free Quote of Ascent Petrochem Holdings Co., Limited

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    Ningbo Changhong SBS CH1401HE is a linear styrene-butadiene-styrene block copolymer supplied as a porous pellet. The grade designation 1401 corresponds to a nominal bound styrene content of 40 wt% in the SBS 1401 series. Melt flow rate is typically reported in the range 0.5–3.0 g/10 min when measured at 200 °C under 5 kg load in accordance with ISO 1133-1:2022; published data for this specific configuration is limited, and incoming lots should be verified against the manufacturer’s certificate of analysis. The product is used primarily in asphalt modification, solvent-borne adhesive compounding, and general-purpose thermoplastic elastomer modification where the stiffness, tensile strength, and hardness of a 40 wt% styrene network are needed. Because the butadiene midblock remains unsaturated, CH1401HE is not inherently oxidation-resistant; antioxidant packages and processing stabilizers are required for long-term thermal service.

    What Distinguishes CH1401HE from Lower-Styrene and Star-Shaped SBS Grades?

    With the styrene block fraction at 40 wt%, CH1401HE is positioned above a 30 wt% styrene SBS 1301 analogue in modulus, tensile strength, and Shore hardness. In a standard compression-molded sheet tested under ISO 37:2017, the higher styrene content raises the nominal tensile strength envelope from roughly 16–20 MPa for 30 wt% styrene grades to approximately 20–26 MPa, while elongation at break shifts downward as the glassy styrene domains restrict chain extension. The 300% modulus also increases because the larger styrene domain fraction raises physical crosslink density. The operational penalty is reduced low-temperature flexibility: a 40 wt% styrene SBS typically exhibits a brittle point approximately 10–15 °C higher than a 30 wt% styrene analogue.

    Against a star-shaped SBS of equivalent styrene content, CH1401HE is a linear architecture. This lowers zero-shear melt viscosity and improves solution flow in solvent-borne adhesives and sealants. Star-shaped grades generally provide higher green strength and better high-temperature creep resistance after processing, whereas the linear CH1401HE is selected for controlled low-viscosity compounding and faster dissolution in aromatic and aliphatic solvent blends. The choice between linear and star-shaped SBS therefore depends on whether the manufacturing constraint is melt pressure and coating rheology or final-part creep resistance.

    Incoming lot control for CH1401HE follows the property envelope shown below. The values are representative of SBS 1401-type linear block copolymers; lot-specific numbers must be taken from the certificate of analysis because published data for this specific configuration is limited.

    PropertyTest methodTypical envelope or limit
    Nominal bound styreneManufacturer FTIR method40±1.5 wt%
    Tensile strengthISO 37:201720–26 MPa
    Elongation at breakISO 37:2017550–700%
    Modulus at 300% elongationISO 37:20172.8–4.0 MPa
    HardnessASTM D2240-1588–94 Shore A
    Melt flow rateISO 1133-1:20220.5–3.0 g/10 min at 200 °C/5 kg
    Volatile matterASTM D5668-21≤0.7 wt%
    AshASTM D5663-21≤0.3 wt%
    Diblock contentManufacturer method≤15 wt%

    Tensile specimens are compression molded and conditioned for 16 h at 23±2 °C and 50±5% RH according to ISO 23529:2016. The presence of diblock above 15 wt% reduces tensile strength and raises melt flow, so diblock content is a critical quality parameter for adhesive dissolution and low-viscosity processing. Volatile matter and ash limits are relevant for hot-melt and solvent-borne applications because excess volatiles generate bubble defects during coating or molding, while ash can interfere with optical clarity and downstream filtration.

    Melt Processing Limits and Vacuum-Drying Requirements

    On a co-rotating twin-screw extruder with an L/D ratio of 36:1 to 44:1, CH1401HE is compounded at barrel temperatures from 150 °C to 190 °C, with a melt temperature limit of 220 °C. At melt temperatures above 230 °C the unsaturated polybutadiene midblock is susceptible to gel formation and chain scission. In production-scale compounding of similar linear SBS grades, screw speed is typically limited to 250–350 rpm at 40–60% torque, and vacuum venting is maintained at -0.08 MPa or lower to strip residual moisture and low-molecular-weight volatiles. Porous pellets absorb moisture under high humidity; pre-drying at 70–80 °C for 2 h is required when storage relative humidity exceeds 60% or when visible surface condensation is present. Uncontrolled moisture in the feed throat produces porosity, melt-pressure fluctuation, and poor pellet-to-pellet lot uniformity.

    For injection molding of CH1401HE compounds, barrel temperatures between 150 °C and 180 °C and mold temperatures between 20 °C and 40 °C are typical. Clamp force requirements scale with projected part area and are not exceptional for SBS; however, the higher styrene content increases melt viscosity relative to lower-styrene SBS and may require an increase in melt temperature or injection pressure of approximately 10–20% when a mold qualified for 30 wt% styrene SBS is reused. Operation above 220 °C should not be used to compensate for viscosity limitations because gel formation accumulates on screw flights, check rings, and hot-runner dead spots.

    On a production-scale asphalt modification line, CH1401HE is added to bitumen at 170–185 °C in a rotor-stator mill. At addition levels of 3.0–5.0 wt%, the polymer phase swells and disperses as a continuous network only after shear is maintained for 45–90 min; a reduction in mixer tip speed below 15 m/s before phase inversion produces storage-unstable binder with polymer-rich domains that separate within 24 h. The critical processing threshold is not merely time-at-temperature but the transition from discrete swollen particles to a co-continuous polymer-rich phase. Softening point typically increases by 15–30 °C over the base bitumen, and elastic recovery at 25 °C reaches 70–90% when tested per ASTM D6084-21 or EN 13398. Storage stability is evaluated by the softening-point difference between top and bottom sections after 72 h at 163 °C; values below 2.5 °C are generally required for hot-storage tanks. Not every bitumen composition responds identically: high-asphaltene sources may require the upper dosage limit or longer pre-shear dwell to reach a stable network.

    When Solvent-Borne Adhesive Compounding Requires Controlled Dissolution Viscosity

    CH1401HE can be dissolved in toluene, cyclohexane, ethyl acetate, or blended aliphatic-aromatic solvent systems for contact adhesives and pressure-sensitive formulations. The linear architecture and controlled diblock content govern dissolution time and final viscosity. A 25 wt% solids solution in toluene at 25 °C typically exhibits a Brookfield viscosity in the range 800–2,500 mPa·s depending on diblock content and molecular weight distribution. Lower-diblock lots dissolve faster and produce lower solution viscosity; higher-diblock lots reduce solution clarity and increase tack but can depress cohesive strength. Production-scale mixing with a high-torque disperser at 300–600 rpm for 4–8 h is sufficient for full dissolution when pellets are added slowly to the vortex; undissolved gel-like centres remain if the pellets are charged too rapidly or if local solvent temperature falls below 15 °C.

    Do not combine CH1401HE with amine-based organic additives that generate free radicals under high shear, as these can initiate premature crosslinking of the unsaturated butadiene block. For adhesive formulations requiring oxidation resistance, hindered phenolic or phosphite stabilizers are preferred. Finished adhesive viscosity should be measured after 24 h equilibration because solution viscosity can drift as the styrene domains fully solvate.

    Blends of CH1401HE with general-purpose polystyrene or polypropylene are not molecularly miscible; however, they are compatible enough to produce useful co-continuous morphologies in footwear compound extrusion at polypropylene contents below 20 wt%. On a single-screw extruder with a compression ratio of 3:1 and die temperature 160–180 °C, the higher styrene content of CH1401HE improves dimensional stability relative to 30 wt% styrene SBS but increases melt pressure by approximately 15–25% at the same screw speed. This operational boundary should be considered when retrofitting a line qualified for lower-styrene SBS. The same compatibility limit applies to filler-modified compounds: calcium carbonate loadings above 30 phr increase viscosity and reduce elongation, but the higher modulus styrene network of CH1401HE retains more hardness and tear strength than lower-styrene SBS at equal filler loading.

    Top