Products

Toray Industries ABS 950-X01

    • Product Name: Toray Industries ABS 950-X01
    • Factroy Site: Yinchuan, Ningxia, China
    • Price Inquiry: sales8@ascent-chem.com
    • Manufacturer: Ascent Petrochem Holdings Co., Limited
    • CONTACT NOW
    VTB
    Specifications
    HS Code 942109
    Manufacturer Toray Industries
    Product Name ABS 950-X01
    Polymer Type Acrylonitrile Butadiene Styrene (ABS)
    Grade 950-X01
    Density 1.04 g/cm³
    Melt Flow Rate 12 g/10 min (220 °C/10 kg)
    Tensile Strength At Yield 44 MPa
    Flexural Modulus 2.2 GPa
    Notched Izod Impact Strength 20 kJ/m²
    Heat Deflection Temperature 82 °C
    Vicat Softening Temperature 98 °C
    Rockwell Hardness R105
    Molding Shrinkage 0.4–0.6 %
    Flammability Rating UL 94 HB
    Processing Method Injection Molding
    Color Natural

    As an accredited Toray Industries ABS 950-X01 factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Toray Industries ABS 950-X01 is supplied in 25 kg moisture-barrier, polyethylene-lined bags, palletized for industrial handling.
    Container Loading (20′ FCL) Toray Industries ABS 950-X01 loaded in a 20′ FCL as palletized 25 kg bags, shrink-wrapped and secured for safe ocean shipment.
    Shipping Toray Industries ABS 950-X01 is typically shipped as non-hazardous ABS resin pellets in moisture-proof bags, sacks, or octabins. Transport under dry, ambient conditions, protected from direct sunlight, excessive heat, and contamination. No UN number or dangerous-goods classification is normally required.
    Storage Store Toray Industries ABS 950-X01 in a cool, dry, well-ventilated area away from direct sunlight, heat sources, moisture, and strong oxidizers. Keep original containers tightly closed, palletized, and protected from physical damage. Prevent dust accumulation and static buildup. Maintain stable temperature and humidity, and follow local fire and material-handling regulations. Do not store near food, drink, or incompatible materials.
    Shelf Life Shelf life is typically 24 months when stored dry, below 30°C, in original sealed packaging, away from sunlight and moisture.
    Free Quote

    Competitive Toray Industries ABS 950-X01 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

    Toray Industries ABS 950-X01 is a transparent methyl methacrylate-modified acrylonitrile–butadiene–styrene resin sold in the Toyolac product family. The numerical designation 950-X01 places the grade in the transparent high-heat ABS segment within Toray’s styrenic portfolio. The product is supplied as cylindrical pellets for injection molding and extrusion. Representative values from the supplier’s technical data sheet include a melt volume-flow rate of 22 cm³/10 min at 220°C and 10 kg load under ISO 1133-1, density of 1.08 g/cm³ under ISO 1183-1, tensile stress at yield of 47 MPa under ISO 527-2/1A, flexural modulus of 2,300 MPa under ISO 178, Charpy notched impact strength of 12 kJ/m² at 23°C under ISO 179/1eA, total luminous transmittance of 90% on a 3 mm injection-molded plaque under ISO 13468-1, and haze of 1.5% under ASTM D1003. These are typical values, not specification limits. The primary structural difference from opaque ABS grades is the incorporation of methyl methacrylate, which reduces the refractive index mismatch between the styrene-acrylonitrile matrix and the dispersed polybutadiene rubber phase. This enables visible-light transmission but lowers notched impact strength compared with opaque high-impact ABS.

    How Does Methyl Methacrylate Modification Affect Optical Transmission and Notch Sensitivity?

    In transparent ABS chemistry, clarity is achieved without removing the polybutadiene rubber phase. The continuous phase is a styrene-acrylonitrile-methyl methacrylate copolymer; the methyl methacrylate unit raises the matrix refractive index and reduces the refractive index difference at the rubber-matrix interface. Light scattering is further suppressed when the dispersed rubber particle diameter is below roughly 300 nm. Published data for the exact rubber particle size distribution in ABS 950-X01 is limited; the optical mechanism is inferred from the general class of methyl methacrylate-modified ABS. The rubber phase remains the source of impact resistance, but its content or particle morphology is constrained by the optical requirement. Consequently, Charpy notched impact strength of 12 kJ/m² at 23°C represents a deliberate balance between clarity and toughness, rather than a processing defect. In comparison, a general-purpose opaque ABS may have a notched impact strength of 20–30 kJ/m² because its rubber particle size and distribution can be optimized for energy absorption without regard for light transmission. The methyl methacrylate modification also increases polarity slightly and reduces low-temperature crack propagation resistance, so sub-zero impact performance should be validated on finished parts rather than inferred from room-temperature data.

    Drying of ABS 950-X01 prior to melt processing is controlled by residual moisture limits. The polymer matrix is not significantly hydrolyzed by water, but excess moisture during injection molding produces splay, silver streaks, and localized haze. A desiccant dryer with a dew point of -40°C or lower is specified. Drying at 80°C for 3–4 h is adequate for material taken from sealed moisture-barrier bags. After ambient exposure above 60% RH, drying should be extended to 4–6 h. Karl Fischer moisture analysis under ISO 15512 should show pellet moisture below 0.05% by weight before melt processing. Higher moisture contents produce visible optical defects without necessarily reducing molecular weight.

    The melt temperature window is 220°C to 250°C at the nozzle. Barrel profiles typically begin at 200°C at the feed throat and increase to 240°C in the metering zone. The maximum allowable melt temperature is 260°C; operation above 250°C accelerates depolymerization of methyl methacrylate segments and oxidation of butadiene unsaturation, producing yellow shift and haze increase before mechanical properties drop sharply. The safe residence time at melt temperature is below 10 min. In hot-runner systems, manifold temperature should be independently limited to 245°C, and gate drool should be controlled by valve-gate timing rather than by increasing manifold heat.

    For reciprocating-screw injection molding, a three-zone screw with an L/D ratio of 20:1 to 24:1 and a compression ratio of 2.0:1 to 2.5:1 is typical. High-compression screws above 2.8:1 can create excessive shear heating and should be validated for optical retention. Back pressure is set at 2–5 MPa, and screw rotation speed is limited to 30–80 rpm to avoid shear-induced yellowness and black specks. Mold temperatures between 40°C and 80°C are applied. Low mold temperatures below 40°C increase internal stress and may raise haze in thick sections; temperatures above 80°C increase cycle time without proportional optical benefit. In thin-wall sections below 1.2 mm, raising melt temperature to 240°C and using injection velocity of 120–180 mm/s can reduce short shots, but the residence-time margin narrows. A two-stage injection profile with lower velocity during the last 10–15% of fill reduces gas traps and gate blush. Pack pressure is typically 50–70% of peak injection pressure for 5–10 s on a 2 mm wall. Overpacking raises molded-in stress and produces visible gate halo. Regrind use is limited to 10–20%; optical applications should use the lower end because repeated thermal history increases yellowness and reduces impact strength. Purging with an acrylic-based purge compound at 220°C after shutdown reduces carbon accumulation. PVC-based purge compounds should be avoided because acidic degradation products contaminate the melt and can corrode mold surfaces.

    Mold shrinkage for tool design is typically 0.4–0.7% along flow and 0.4–0.8% transverse, depending on wall thickness, gate location, and processing conditions. For a 2 mm wall thickness, the flow-length-to-wall-thickness ratio for transparent ABS is generally below that of high-flow opaque ABS but above that of polycarbonate. Capillary rheometry of the transparent ABS class at 230°C typically shows shear-thinning behaviour with apparent viscosity falling from around 300 Pa·s at 100 s⁻¹ to below 100 Pa·s at 1,000 s⁻¹. Published data for ABS 950-X01 specifically is limited; mold-filling simulation should be calibrated with lot-specific capillary rheometry. Batch-to-batch optical haze variation of approximately ±0.3% at 3 mm is common for transparent ABS grades. When mating parts are molded from different lots, visual inspection under controlled illumination is recommended.

    Representative property comparison between ABS 950-X01 and general-purpose opaque ABS
    PropertyTest methodABS 950-X01Opaque general-purpose ABS
    Melt volume-flow rate, 220°C, 10 kgISO 1133-122 cm³/10 min15–25 cm³/10 min
    DensityISO 1183-11.08 g/cm³1.04–1.06 g/cm³
    Tensile stress at yieldISO 527-2/1A47 MPa42–50 MPa
    Flexural modulusISO 1782,300 MPa2,000–2,400 MPa
    Charpy notched impact strength, 23°CISO 179/1eA12 kJ/m²20–30 kJ/m²
    Total luminous transmittance, 3 mmISO 13468-190%<5%
    Haze, 3 mmASTM D10031.5%opaque
    Vicat softening temperature, 50 NISO 306/B5096°C98–102°C

    When the Melt Temperature Exceeds 250°C in a Hot-Runner Tool

    Thermal degradation in methyl methacrylate-modified ABS is a process conflict because the same heat that reduces melt viscosity for thin-wall filling also accelerates depolymerization and chromophore formation. At melt temperatures above 250°C, the yellowness index can increase measurably within 5–10 min of residence time. The processing window is consequently narrower than for opaque ABS. In hot-runner tools, temperature overshoot at the gate tip can produce yellow streaks and black specks even when the barrel setpoint remains within range. Independent zone control should limit the manifold to 245°C, and thermocouple placement should be verified with a needle pyrometer on the nozzle adapter. If gate drool occurs, the first correction is valve-gate timing, not increased manifold temperature. Degraded material is removed by purging with an acrylic-based purge compound at 220°C, followed by short shots of natural ABS to confirm visual cleanliness. Leaving material in the barrel during production interruptions longer than 15 min at melt temperature is not recommended. For interruptions longer than 30 min, heat is reduced to 160°C or the barrel is purged and cooled.

    Oxidation of the polybutadiene phase follows radical chain chemistry; primary antioxidants are present in the formulation, but their depletion is time-temperature dependent. Published specific oxidation induction time data for ABS 950-X01 is limited, so the boundaries above are based on the general transparent ABS class and should be confirmed with lot-specific trials. Transparent ABS grades can deposit volatile oligomers on the mold surface; production lines often clean polished optical cavities after 5,000–10,000 shots with a solvent-free alkaline mold cleaner to maintain haze below specification. Silicone-free ejector pin lubricants are used because oil-based lubricants migrate and produce visible fogging. Vent depths of 0.02–0.03 mm are typical for transparent ABS; insufficient venting causes gas burn marks that are immediately visible in clear parts. Vacuum venting may be used for optical surfaces. On a 120 t machine with a 35 mm screw, a two-cavity cold-runner tool with shot weight below 80 g is within the processing envelope for many optical parts.

    Material compliance documentation for ABS 950-X01 is lot-specific. The supplier typically provides statements for RoHS Directive 2011/65/EU as amended by (EU) 2015/863 and for REACH Regulation (EC) No 1907/2006 Article 33 candidate list. Flammability classification is usually UL 94 HB at 1.6 mm; the UL Yellow Card should be consulted for exact valid thickness and colour. For food-contact components, verification under FDA 21 CFR 177.1020 is required at the finished-article level because migration test results depend on surface-to-volume ratio, contact time, and final additives. For medical housings that involve skin contact or short-term tissue contact, cytotoxicity and irritation evaluation under ISO 10993-5 and ISO 10993-10 are end-user responsibilities; the raw material supplier does not make a finished-device biocompatibility claim. The grade is not intended for long-term implantation or for prolonged contact with ketones, esters, aromatic hydrocarbons, or chlorinated solvents. Such solvents cause environmental stress grazing, especially in the presence of molded-in stress. Annealing at 65°C for 2 h before solvent bonding or adhesive joining reduces the tendency for stress cracking. Cyanoacrylate adhesives should be validated under load, because their vapour can cause microcrazes in transparent ABS.

    Compliance and standard verification matrix
    RequirementStandard or regulationVerification responsibility
    Restriction of hazardous substancesRoHS 2011/65/EU + (EU) 2015/863Supplier declaration per lot
    REACH candidate listRegulation (EC) No 1907/2006 Article 33Supplier statement per lot
    FlammabilityUL 94HB at 1.6 mm, UL Yellow Card
    Food-contact migrationFDA 21 CFR 177.1020Finished-article test
    BiocompatibilityISO 10993-5, ISO 10993-10End-user validation
    Moisture contentISO 15512<0.05% by weight
    Optical transmittanceISO 13468-190% at 3 mm
    HazeASTM D10031.5% at 3 mm

    Difference from Polycarbonate and MABS in Clear Thin-Wall Applications

    ABS 950-X01 is not a direct substitute for bisphenol-A polycarbonate where continuous-use temperatures above 120°C or very high impact strength are required. The Vicat softening temperature of 96°C under ISO 306/B50 and Charpy notched impact strength of 12 kJ/m² place it below typical polycarbonate values of approximately 145°C and 60–70 kJ/m². The grade nonetheless offers lower melt viscosity, lower processing temperature, lower density, and a polymer backbone that does not contain bisphenol A. In thin-wall optical housings where the thermal load is below 60°C and impact events are moderate, these differences can justify substitution on a cost-and-density basis. Compared with MABS grades, the 950-X01 designation generally indicates higher stiffness and heat resistance within Toray’s transparent styrenic range. Published data comparing 950-X01 with every Toyolac transparent grade is limited; users should compare lot-specific datasheets for flow-length ratio, haze, and notched impact before substituting. The flexural modulus of 2,300 MPa provides snap-fit deflection recovery at ambient temperature, but long-term creep at temperatures above the glass transition onset of the styrenic matrix is more pronounced than in polycarbonate. For optical applications requiring colour stability under blue LED exposure, published data for this specific grade is limited; accelerated testing under the intended light spectrum and temperature is required.

    Typical application evaluations for ABS 950-X01 include clear diagnostic cuvettes, optical windows for point-of-sale scanners, cosmetic packaging, small appliance lenses, and printer status light covers. In these parts, the combination of 90% total luminous transmittance and 2,300 MPa flexural modulus allows snap-fit assembly without gross creep at room temperature. However, continuous load at temperatures above 60°C is an operational boundary; creep modulus decreases more rapidly than for polycarbonate. For light-emitting diode applications, the yellowness index on 3 mm plaques is typically below 2; colour shift after 1,000 h of blue LED exposure at 50°C has not been published for this specific grade and should be evaluated on final parts. Colour concentrates with styrene-based carriers are preferred; polyolefin carrier resins can reduce transparency and create visible delamination at gate areas. Laser marking with a 1064 nm Nd:YAG system produces dark contrast on transparent ABS, but contrast is lower than on opaque grades. Ultrasonic welding of transparent ABS uses a shear joint design with amplitude below 20 µm at 20 kHz to avoid microcracking at the joint. Solvent bonding with cyclohexanone or methylene chloride is possible but requires pre-annealing at 65°C for 2 h to reduce molded-in stress. For gamma sterilization of clear medical housings, published data for this specific configuration is limited; validation under ISO 11137 is required. After gamma exposure, transparent styrenic grades may show yellowing, and the degree depends on radiation dose and stabilizer formulation. Electron-beam sterilization may cause less colour shift but should also be validated on the finished device.

    Top