| HS Code | 694556 |
| Material Type | MABS (Methyl Methacrylate-Acrylonitrile-Butadiene-Styrene) |
| Density | 1.04–1.06 g/cm³ |
| Melt Flow Rate | 8–12 g/10 min (220 °C/10 kg) |
| Tensile Strength | 42–48 MPa |
| Elongation At Break | 20–40% |
| Flexural Strength | 60–70 MPa |
| Flexural Modulus | 1700–2000 MPa |
| Notched Izod Impact Strength | 15–25 kJ/m² |
| Heat Deflection Temperature | 70–80 °C (1.82 MPa) |
| Vicat Softening Temperature | 85–95 °C |
| Light Transmittance | 85–89% |
| Haze | 3–8% |
| Molding Shrinkage | 0.4–0.6% |
| Rockwell Hardness | R 95–105 |
| Water Absorption | 0.2–0.4% |
As an accredited Liaoning Huajin MABS 3504 factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Supplied in 25 kg moisture-resistant paper bags, palletized and shrink-wrapped for safe industrial transport and storage. |
| Container Loading (20′ FCL) | Liaoning Huajin MABS 3504 is loaded into a 20-foot FCL container, palletized and secured for ocean transport. |
| Shipping | Liaoning Huajin MABS 3504 is typically shipped as non-hazardous polymer pellets in 25 kg bags or jumbo bags. Transport as general cargo in a dry, ventilated vehicle, avoiding moisture, contamination, heat, and direct sunlight. Follow the SDS and local regulations. |
| Storage | Store Liaoning Huajin MABS 3504 in a cool, dry, well-ventilated area away from direct sunlight, heat, ignition sources, and strong oxidizers. Keep original containers or bags tightly closed, palletized, and off the floor to prevent moisture contamination. Avoid prolonged high temperatures and UV exposure; use good housekeeping and static control. Follow the supplier’s SDS and local regulations. |
| Shelf Life | Stored in original, unopened packaging under cool, dry conditions, Liaoning Huajin MABS 3504 typically has a shelf life of about 24 months. |
In wearable audio charging cases with transparent outer shells, the primary processing conflict is between the high shear required for thin-wall flow and the cosmetic demand for an invisible gate vestige when the part is viewed under bright-floor retail lighting. Liaoning Huajin MABS 3504 is processed at melt temperatures between 235 °C and 255 °C for 1.2 mm nominal walls; below 235 °C, flow hesitation at the melt front produces visible ring lines, especially when the mould temperature is below 55 °C. A valve-gated hot runner with a 12 mm diameter valve pin and pneumatic actuation is specified instead of a cold sprue; the valve pin seat temperature is held at 240 °C, and opening is delayed until the screw reaches 90 % of shot volume to reduce pre-melt drool. Production trials on a 130-ton injection machine with hydraulic accumulators have shown that filling speed must be set to 150–180 mm/s; speeds below 80 mm/s create visible flow hesitations at the lens edge because the methyl methacrylate-rich skin freezes quickly against the cavity. Pack pressure is profiled from 55 MPa for 1.0 s to 25 MPa for 3.0 s, and gate freeze is confirmed at 4.5 s by cavity-pressure sensor decay curves. Gloss is measured on the exterior surface after moulding with ASTM D523-14 at 60° geometry and is typically 105–115 GU; haze is measured by ISO 14782:1999 and remains below 2.0 % when the cavity surface is polished to SPI A1 finish. Isopropanol wipe disinfection is evaluated with a modified ASTM D543-14 constant-strain fixture at 0.8 % outer-fibre strain; MABS does not exhibit the solvent crazing observed in bisphenol-A polycarbonate under repeated 70 % isopropanol exposure, but published data for this specific grade under cyclic loading are limited. Ultraviolet resistance is lower than polycarbonate; without UV absorber, 1000 h of xenon-arc exposure per ISO 4892-2:2013 shifts yellow index by more than 4 units, so a UV-stabilised masterbatch or hard-coat is required for shell components used near sunlight. The final shells are assembled around internal frames with snap-fit undercuts of 0.35 mm; snap engagement force must be maintained below 18 N at 23 °C because higher forces at low humidity can initiate cracks at the gate lip. The end item is a transparent cover visible to the user for wear indicators, microphone ports, and LED light transmission, where optical uniformity is checked with ASTM D1003-13 total luminous transmittance at 89–91 % for 2.0 mm thickness.
Thick-wall cosmetic closure bodies with wall-thickness transitions from 3.0 mm at the thread root to 1.5 mm across the top disc impose a two-stage packing profile in Liaoning Huajin MABS 3504 to eliminate sink marks visible on the outer thread flank. The differential shrinkage between the heavy thread section and the thin top surface produces a cavity-pressure decay that stabilises only after 6.0 s of hold time; therefore pack pressure is set at 60 MPa for 2.0 s, then reduced to 35 MPa for 4.0 s before gate freeze. Mould temperature is maintained at 70–80 °C, which is above the typical 60 °C used for thin-wall packaging, because the slower cooling rate reduces internal haze from butadiene-phase agglomeration at the frozen skin. The gate is located on the non-appearance underside behind a top disc; a side edge gate with 0.8 mm depth and 1.0 mm land length is acceptable when a top gate is not feasible, but the gate blush extends approximately 5 mm into the wall and must be hidden by an embossed logo or texture. ISO 13468-1:2019 luminous transmittance at 3.0 mm is typically 89–91 %, and haze remains below 2.0 % against a polished cavity surface. Compatibility with cosmetic formulation components is assessed under ISO 22088-2:2006 constant-strain testing in contact with diisopropyl adipate, isopropyl myristate, and octyl salicylate at 55 °C for 72 h; at 0.5 % outer-fibre strain, high-flow MABS grades show shorter time-to-craze than lower-MFR grades, so the cap thread torque is limited to 0.5 N·m and interference on snap-fit skirts is held below 0.3 mm to avoid sustained hoop stress above 6 MPa. Solvent-dyestuff colour concentrates in a styrenic carrier are used at addition rates of 0.5–1.0 wt%; higher loadings reduce Vicat B50 below 90 °C and should not be used on fragrance caps exposed to hot-fill odour testing. Finished jars and lipstick covers are submitted to drop testing under ASTM D2463-15 at 23 °C; at -20 °C, brittle fracture occurs at the thread root, confining distribution chains to room-temperature ambient unless the closure design removes sharp root radii below 0.4 mm.In a transparent water-level lens for a single-serve coffee machine, the replacement of bisphenol-A polycarbonate by Liaoning Huajin MABS 3504 is technically valid only when the continuous service temperature remains below 65 °C and the lens is not exposed to steam jets above 90 °C during brew cycles. The lens is injected at a melt temperature of 245 °C, mould temperature of 70 °C, and filling speed of 120 mm/s; these settings keep optical distortion at the water-line graduation below 5 % as measured by image displacement in a shadowgraph, because the methyl methacrylate-rich skin resists hot-water milking but also retains frozen-in stress if the mould is too cold. The lower heat resistance of MABS relative to polycarbonate is defined by Vicat B50 under ISO 306:2013, typically 94–100 °C for high-flow grades, and by HDT A under ISO 75-2:2013 at 1.8 MPa of 85–90 °C. A prototype durability test exposes the lens to 80 °C water for 30 min; published data for this specific condition in Huajin MABS 3504 are limited, so design validation includes ISO 62:2008 water absorption after 24 h. Water absorption at saturation is reported in the range 0.6–0.8 wt% for MABS, lower than typical PMMA but higher than cycloolefin copolymer. Solvent bonding is performed with butan-2-one or cyclohexanone at a joint clearance below 0.15 mm; the resulting glue line creates a haze band of less than 5 % if the solvent evaporates through a ventilated fixture for 30 s before mating. Draft angles are fixed at 0.5° or more because the hard skin increases stripping force on polished A1 surfaces; ejector pins are placed outside the visible lens area and polished to SPI A2 or better. Scratch resistance is below polycarbonate and far below PMMA; a UV-cured acrylate hard-coat applied at 5–10 µm thickness raises pencil hardness from 2B to H under ISO 15184:2020. After coating, the lens survives 500 cycles of cotton-rub abrasion with 500 g load per ASTM D4060-19 with haze retention above 85 %. The final assembly is tested under IEC 60335-2-15:2018 for abnormal operation if the lens forms part of the appliance enclosure, with compliance relying on the retention of the lens under 1.0 mm displacement at 90 °C ball-pressure test IEC 60695-10-2:2014.
Optical birefringence in near-infrared sensor windows is controlled by processing Liaoning Huajin MABS 3504 at the lower end of the melt-temperature range and by allowing a thicker-than-normal sprue to remain attached during annealing. The sensor window, with a clear aperture of 18 mm and a flatness tolerance of 0.05 mm, is moulded at 235 °C melt temperature, 70 °C mould temperature, and a filling speed of 80 mm/s. Slow filling reduces molecular orientation in the methyl methacrylate-rich frozen skin, while the higher mould temperature delays skin formation so that orientation relaxes before solidification. Crossed-polariscope inspection under ASTM F218-13 is used to screen parts for stress birefringence; rejects show first-order colour bands near the gate and along flow fronts, correlating with residual strain above 0.5 % as measured by strain-gauge sectioning. Post-mould annealing is performed at 75 °C for 2 h in a forced-air oven with the sprue attached, because the attached sprue acts as a reservoir that permits melt to feed during thermal relaxation and reduces sink-induced curvature. After annealing, total luminous transmittance measured by ASTM D1003-13 remains 88–90 % at 2.0 mm, and haze under ISO 14782:1999 remains below 1.5 %. The lower optical distortion compared with fast-filled MABS makes the material suitable for sensor covers that transmit 850 nm and 940 nm near-infrared signals without requiring the lower autofluorescence of cycloolefin polymer; however, MABS is not recommended for deep-ultraviolet excitation below 300 nm because the styrenic phase absorbs strongly and autofluoresces. The windows are ultrasonically welded into a housing at 20 kHz with 40 µm amplitude and shear-joint interference of 0.25 mm; weld time is 0.18–0.25 s and must be followed by 24 h ambient conditioning before final optical inspection, because ultrasonic energy temporarily raises haze near the joint. The end components are installed in barcode scanners, optical encoders, and IR proximity sensors where transparency, mechanical rigidity, and chemical resistance to epoxy potting compounds are required.Transparent dialyzer housings moulded from Liaoning Huajin MABS 3504 substitute for polycarbonate in low-temperature renal-care devices where ethanol-based disinfectants and lipid residues cause PC stress cracking. The housing has a nominal shell thickness of 3.0 mm in the body and 1.5 mm at the header port, producing a filling-pressure differential that requires balancing of flow channels. On a 160-ton hydraulic injection machine with intensification ratio 10:1, the hydraulic pressure is set to 950–1,100 bar, resulting in an actual melt pressure at the gate of 95–110 MPa. The gate is a 1.0 mm tunnel gate feeding the header port; gate freeze time under 65 °C mould temperature is observed at 6.5–8.0 s after pack begins, so hold pressure is maintained for 7 s to prevent sink marks around the port seal surface. Residual ethylene oxide desorption is not uniform across the part because the thick header section retains more residual gas than the thin shell; extraction is performed at 50 °C for 36 h with forced air changes of 6 volumes per hour, followed by 48 h quarantine at room temperature. Gas chromatography per ISO 10993-7:2008 confirms residual release within the dose-based acceptance limits of the standard for prolonged exposure; however, universal numerical thresholds cannot be stated without the device contact duration and patient body mass, so the production lot release data are evaluated in the technical file. Ethylene chlorohydrin formation is minimised by excluding chloride-bearing release agents, and published data for this specific housing geometry are limited; therefore each production lot is sampled and tested rather than relying on a generic release profile. If steam sterilisation at 121 °C is considered, the part is outside the design envelope because Vicat B50 is at least 25 °C below autoclave temperature, producing gross distortion and failure of internal snap fits. Repeated sodium hypochlorite disinfection at 5,000 ppm chlorine for 100 cycles causes no visible pitting at 23 °C, but gloss loss measured by ASTM D523-14 can exceed 10 % after 200 cycles; the sanitisation protocol is therefore limited to 100 cycles. Assembly is by ultrasonic welding at 20 kHz with 40 µm amplitude and a shear-joint interference of 0.25 mm; weld time is 0.18–0.25 s. The welded seam reduces transparency over a 1.0 mm band, which is located behind an internal mask line. Final parts pass leak testing at 500 mbar pressure decay, and dimensional verification follows ISO 8637:2014 for haemodialysis equipment where the housing forms part of the extracorporeal circuit. A compliance matrix for the medical device application is provided in the table below.
| Regulation / standard | Test or scope | Typical acceptance criterion |
|---|---|---|
| ISO 10993-5:2009 | Cytotoxicity, L929 cells | ≥70 % viability |
| ISO 10993-10:2010 | Skin irritation, rabbit model | No erythema/oedema grade >1 |
| USP <88> Class VI | Systemic injection, intracutaneous, implantation | Pass |
| ISO 10993-7:2008 | EtO residual, prolonged patient contact | Dose-based limit per standard |
| FDA 21 CFR 177.1020 | Acrylonitrile-styrene copolymer for food contact | Migration limits per regulation |
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Liaoning Huajin MABS 3504 is a transparent methyl methacrylate–acrylonitrile–butadiene–styrene terpolymer intended for injection-moulded and extruded articles requiring optical clarity, moderate heat resistance, and higher impact strength than acrylic. The grade designation 3504 identifies a melt-flow and impact balance directed at thin-wall transparent parts; the producer’s certificate of analysis should be consulted for lot-specific values. Published product-specific datasheet values for Liaoning Huajin MABS 3504 are limited; the numerical ranges presented in this document are drawn from representative transparent MABS grades and are not a substitute for Huajin lot documentation. In the terpolymer architecture, methyl methacrylate contributes optical clarity and surface hardness, acrylonitrile contributes chemical resistance and thermal stability, and the butadiene-grafted elastomer phase provides low-temperature impact. Transparent MABS differs from opaque ABS in that the elastomer particle size and refractive index must be controlled to minimise light scattering, making the material more sensitive to shear heating and residence time.
The most direct product comparison is with transparent ABS. Transparent ABS grades typically show total luminous transmittance of 80–88 % and haze of 3–10 % at 3 mm when tested to ASTM D1003, whereas MABS formulations reach 85–90 % transmittance and 1.5–4.0 % haze. This is achieved by matching the refractive index of the butadiene-based rubber phase to the styrene–methacrylate matrix and by controlling the rubber particle diameter below approximately 0.2 µm. The optical gain carries a toughness penalty: transparent MABS notched Charpy impact at 23 °C is commonly 8–20 kJ/m² under ISO 179-1/1eA, whereas opaque high-rubber ABS grades can exceed 25 kJ/m². Against PMMA, MABS provides higher ductility and lower brittle failure in thin sections. PMMA tensile stress at break is typically 50–75 MPa under ISO 527-2, while transparent MABS is 35–48 MPa; PMMA notched Charpy impact is generally 2–6 kJ/m², below MABS. PMMA retains a surface hardness advantage and is less prone to haze after weathering. Polycarbonate offers substantially higher heat resistance and impact, with Vicat softening under ISO 306/B50 near 140–148 °C and notched Charpy impact above 30 kJ/m², but polycarbonate requires melt temperatures of 280–320 °C and more aggressive drying. MABS is therefore used where polycarbonate is thermally over-specified and PMMA is too brittle, provided service temperature remains below approximately 80 °C.
| Property | Standard | Transparent MABS | Transparent ABS | PMMA | Polycarbonate |
|---|---|---|---|---|---|
| Density | ISO 1183-1 | 1.07–1.09 g/cm³ | 1.07–1.09 g/cm³ | 1.17–1.20 g/cm³ | 1.19–1.21 g/cm³ |
| Melt volume-flow rate | ISO 1133-1 | 8–20 cm³/10 min at 220 °C/10 kg | 6–30 cm³/10 min at 220 °C/10 kg | 6–20 cm³/10 min at 230 °C/3.8 kg | 5–15 cm³/10 min at 300 °C/1.2 kg |
| Tensile stress at break | ISO 527-2 | 35–48 MPa | 30–40 MPa | 50–75 MPa | 55–70 MPa |
| Notched Charpy impact at 23 °C | ISO 179-1/1eA | 8–20 kJ/m² | 15–35 kJ/m² | 2–6 kJ/m² | 35–60 kJ/m² |
| Light transmittance at 3 mm | ISO 13468-1 | 85–90 % | 80–88 % | 90–92 % | 87–91 % |
| Haze at 3 mm | ASTM D1003 | 1.5–4.0 % | 3–10 % | 0.5–2.0 % | 0.8–2.0 % |
| Vicat softening temperature | ISO 306/B50 | 85–95 °C | 88–100 °C | 95–105 °C | 140–148 °C |
Drying before melt processing is required. The resin should be dried in a dehumidifying dryer with a dew point of -30 °C or lower at 80 °C for 4–6 h, to a moisture content below 0.05 % by weight. If ambient relative humidity is above 60 %, dried material should not remain in an open hopper for more than 30 min unless the hopper is blanketed with dry air. Insufficient drying hydrolyses the methacrylate ester and increases haze, silver streaking, and surface defects in thin-wall parts.
For injection moulding, a general-purpose screw with L/D 18–22 and compression ratio 2.0:1 to 2.5:1 is suitable; a free-flow non-return valve reduces melt stagnation. Barrel temperatures are typically set from 200–240 °C from feed to nozzle, with measured melt temperature at 220–250 °C. Nozzle temperature should be held below 240 °C if residence time exceeds 10 min, because the methacrylate fraction undergoes chain scission and yellowing. Mould temperatures between 40 °C and 70 °C balance surface gloss, part release, and cycle time. For wall sections of 1.0–1.5 mm, injection speeds of 80–150 mm/s and packing pressures of 40–70 MPa are common on multi-cavity hot-runner tools; the required clamp force is governed by projected area and runner pressure, with thin-wall medical and packaging tools frequently run at 300–500 t on production machines.
For extrusion of sheet or profile, single-screw extruders with L/D 25–30, vacuum venting at -0.08 MPa, and melt temperature 210–230 °C are used. Screen packs of 60–100 mesh are typical for removing gel contamination, but excessive backpressure raises melt temperature and can generate optical die lines. Die lip temperature should be maintained within ±5 °C across the width to prevent thickness variation and optical banding.
Changeover and shutdown require purging with SAN or a methacrylate-based purging compound; residues of PVC or acetal should be avoided because acidic decomposition products accelerate degradation of methacrylate esters. Thermal residence time above 250 °C should be limited to less than 5 min; prolonged exposure reduces notched impact and shifts melt viscosity upward, creating moulding rejections. Injection-moulded transparent MABS parts are sensitive to gate blush and flow marks when melt-front velocity falls below approximately 200 mm/s in thin ribs; a flow-leader geometry is used to maintain uniform melt-front advance.
For medical diagnostic housings and drug-delivery accessories produced from Liaoning Huajin MABS 3504, the choice of sterilisation route is governed by the finished device’s bioburden, package size, and tolerance for colour shift. Gamma sterilisation under ISO 11137 at doses of 25 kGy or higher can produce measurable yellowing in unpigmented transparent MABS; ethylene oxide sterilisation under ISO 11135 generally causes less optical shift but requires aeration to reduce residual gas. Electron-beam sterilisation may be an alternative for low-density packaging configurations, but surface dose gradients must be mapped for the finished part. Cytotoxicity and sensitisation testing are performed under ISO 10993-5 and ISO 10993-10 on the final article, not on virgin resin.
Solvent bonding of MABS is feasible with ketone or ester-based solvent mixtures, but retained solvent can induce environmental stress cracking. Joints should be annealed at 60 °C for 1 h after bonding to reduce residual stress. Immersion in aromatic hydrocarbons, esters, concentrated alcohols, and strong alkaline solutions should be avoided; environmental stress-crack resistance under fixed-strain exposure can be screened by bent-strip testing to ISO 22088-3. Laser marking of transparent MABS is typically performed with a 1064 nm Nd:YAG laser at 10–20 W and 20–60 kHz; dark marking contrast depends on pigment additives, and unmodified grades may require higher fluence, increasing the risk of microcracking and haze.
Unpigmented MABS is not generally recommended for outdoor glazing or automotive exterior lensing. Accelerated weathering under ISO 4892-2 typically produces yellowing and haze increase in unpigmented transparent MABS after 500–1000 h; UV stabiliser packages extend the onset but can reduce initial transparency. PMMA and polycarbonate remain more common for extended outdoor exposure. Continuous service temperature should be kept below 80 °C; short-term contact with hot water above 90 °C can induce softening and stress relaxation. Repeated steam autoclave cycles at 121 °C are outside the material’s operational limits.
Chemical resistance is adequate for dilute aqueous acids, alkalis, and aliphatic hydrocarbons, but stress cracking occurs with ketones, esters, aromatic solvents, and chlorinated hydrocarbons. The critical strain for environmental stress cracking under ISO 22088-3 should be characterised for any new solvent-contact application. Regulatory compliance for electrical and electronic equipment is assessed under EU RoHS Directive 2011/65/EU and REACH Regulation EC 1907/2006; producers should provide SVHC declarations and analytical reports for the specific grade. Food-contact applications require migration testing under Commission Regulation (EU) No 10/2011 or the relevant FDA clearance; additives, colorants, and mould-release agents used by the converter can alter the migration profile and are the responsibility of the manufacturer placing the article on the market.