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Anhui Liwei Chemical Co., Limited.

EVOH EVAL SP482B

    • Product Name: EVOH EVAL SP482B
    • Factroy Site: Lingwu, Yinchuan, Ningxia, China
    • Price Inquiry: sales2@liwei-chem.com
    • Manufacturer: Anhui Liwei Chemical Co., Limited.
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    Specifications
    HS Code 703437
    Product Name EVOH EVAL SP482B
    Material Type Ethylene vinyl alcohol copolymer
    Ethylene Content 48 mol%
    Melt Flow Rate 3.0 g/10 min (190°C, 2.16 kg)
    Density 1.17 g/cm³
    Melting Point 164 °C
    Crystallization Temperature 143 °C
    Glass Transition Temperature 58 °C
    Tensile Strength At Break 62 MPa
    Elongation At Break 250%
    Oxygen Transmission Rate 0.4 cm³·mm/(m²·day·atm) at 20 °C, 65% RH

    As an accredited EVOH EVAL SP482B factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing EVOH EVAL SP482B is supplied in 25 kg sealed multi-layer paper bags, protected from moisture and contamination.
    Container Loading (20′ FCL) EVOH EVAL SP482B loaded in 20′ FCL, palletized, secured, with proper ventilation and moisture protection to ensure safe transport.
    Shipping EVOH EVAL SP482B is a non-hazardous ethylene vinyl alcohol copolymer resin supplied in sealed, moisture-resistant bags or containers. Ship in dry, ventilated conditions, avoiding direct sunlight and extreme heat. Protect from moisture and physical damage; handle with standard industrial hygiene practices to prevent dust generation.
    Storage Store EVOH EVAL SP482B in its original, tightly sealed containers in a cool, dry, well-ventilated area. Protect from moisture, direct sunlight, and excessive heat to prevent degradation. Maintain moderate temperatures and avoid contamination. Use within the manufacturer’s recommended shelf life, ensuring containers are properly resealed after each use.
    Shelf Life Store in a cool, dry place away from sunlight. Shelf life is two years from manufacture date when container remains unopened.
    Application of EVOH EVAL SP482B

    In a five-layer cast coextrusion line producing retortable stand-up pouches, the structure is sequenced as PP / anhydride-grafted PP tie / EVAL SP482B / tie / PP, with the EVOH core set at 12 µm inside a total film thickness of 85 µm. The oxygen transmission rate objective is 2.0 cm³·20 µm/(m²·day·atm) at 23 °C and 0 % RH when measured according to ASTM D3985. SP482B pellets are pre-dried in a desiccant dryer with a dew point of -40 °C for 4 h at 90 °C to reach a residual moisture level below 0.04 % by Karl Fischer titration per ISO 15512. The barrier extruder is a 50 mm single-screw machine with an L/D of 30 and a three-zone barrier screw; barrel temperatures are profiled from 180 °C at the feed throat to 225 °C at the metering section, and the feedblock is held at 230 °C. The die gap is set at 0.8 mm and the cast line runs at 45 m/min to achieve the target gauge. Tie layers of anhydride-grafted PP are maintained at 5 µm each and are required because SP482B does not develop sufficient peel strength to PP without a functionalized intermediate layer; peel strength measured by ASTM F904 remains between 4.0 and 6.0 N/15 mm on as-cast film. The inner food-contact PP layer at 28 µm meets EU Regulation 10/2011 overall migration limits below 10 mg/dm², and the structure is compliant with FDA 21 CFR 177.1360 when the EVOH layer is separated from food by a functional barrier. After pouch fabrication, retort processing at 121 °C for 30 min introduces moisture into the polyolefin layers; water vapor reaching the EVOH core raises its oxygen transmission rate, but the target remains below 2.0 cm³·20 µm/(m²·day·atm) because the PP skins reduce humidity ingress before the core is saturated. Post-retort pouch burst testing per ASTM F1140 and seal strength testing per ASTM F88 are used to detect delamination between EVOH and tie layers; acceptable seal strength after retort is 1.5–3.0 N/15 mm for easy-open lidding features. Long-term ambient storage tests at 25 °C and 60 % RH are conducted for 12 months to verify stability of oxygen-sensitive food formulations.

    LayerMaterialNominal thicknessFunction
    Outer skinPP homopolymer35 µmMoisture barrier, print surface
    TieAnhydride-grafted PP5 µmAdhesion to EVOH
    Barrier coreEVAL SP482B12 µmOxygen barrier
    TieAnhydride-grafted PP5 µmAdhesion to EVOH
    Inner food-contact layerPP random copolymer28 µmSealant, food contact

    What Causes Layer Waviness in 15 µm SP482B Cores When Coextruded with LLDPE at Draw-Down Ratios Above 3.5:1?

    When the core is thinned below 15 µm and the structure is drawn down from 0.9 mm die gap to 9 mm final blown film thickness, the velocity gradient in the film blowing process amplifies viscosity mismatch between SP482B and LLDPE. SP482B exhibits a melt flow rate in the range 8–15 g/10 min at 190 °C / 2160 g per ASTM D1238, whereas butene-LLDPE grades commonly run at 1–2 g/10 min under the same conditions. This creates a viscosity ratio greater than 10:1 at the die exit, causing the lower-viscosity EVOH to migrate toward higher shear rate regions and produce sinusoidal layer waviness. Optical microscopy of polished microtome sections shows core-layer thickness variation exceeding ±3 µm across a 10 mm transverse field when draw-down exceeds 3.5:1; this is the typical onset threshold for drop-lamination defects in printed laminates. To reduce waviness, the die temperature is lowered from 225 °C to 215 °C, the blow-up ratio is kept at 2.2–2.5, and the frost line height is reduced to 450 mm. Tie-layer thickness is increased from 3 µm to 5 µm because the added interfacial layer distributes stress more uniformly. On a 70 mm three-layer blown film line with a spiral mandrel die, melt pressure fluctuations above 5 % of mean value indicate layer re-arrangement and require adjustment of the EVOH extruder zone from 220 °C to 200 °C or reduction of screw speed by 10 %. Post-process oxygen transmission testing per ASTM D3985 at 23 °C and 0 % RH is used to confirm that the actual barrier layer thickness remains sufficient; wavy zones with core thickness below 8 µm show oxygen transmission above the desired 2.0 cm³·20 µm/(m²·day·atm) ceiling and are rejected during statistical process control sampling.

    During six-layer blow molding of HDPE fuel tanks on an accumulator-head machine, EVAL SP482B is metered into the barrier layer at 3 wt% of the total parison wall thickness through a 35 mm barrier extruder operating at a melt temperature of 220 °C. The layer sequence is HDPE outer / anhydride-grafted PE tie / SP482B / tie / regrind-HDPE / HDPE inner. The accumulator head is held at 220–225 °C and the parison drop time is kept below 20 s to prevent gel formation in the barrier layer. SP482B is pre-dried at 90 °C for 5 h to below 0.04 % residual moisture because water in the melt hydrolyzes vinyl alcohol units and generates acetic acid odor, voids, and interfacial adhesion loss. Fuel permeation performance is evaluated according to SAE J1737 vehicle fuel system permeation test procedures, and oxygen ingress into the tank headspace is measured by ASTM D3985 on blow-molded wall sections cut from the tank sidewall. The high ethylene content of SP482B, 48 mol%, provides a broader processing window than 32 mol% EVOH but raises the equilibrium oxygen transmission; tank wall oxygen transmission is accepted when below 2.5 cm³·20 µm/(m²·day·atm) at 23 °C and 50 % RH. Regrind addition up to 30 % is typically used in HDPE fuel tank production; published data for SP482B dispersion in high-regrind barrier-layer streams is limited, so the layer distribution is confirmed by microtome sectioning and polarized light microscopy before production release. The EVOH layer is not crosslinked; therefore, tank wall impact performance at -40 °C is verified per ISO 6603-2 puncture impact testing to ensure that the barrier core does not crack during low-temperature vehicle operation. Barrier-layer adhesion is checked after 60 s of exposure to a 50 °C water bath; peel strength below 2.0 N/15 mm per ASTM F904 indicates moisture-induced delamination at the tie interfaces. The process boundary is defined by a maximum melt temperature of 240 °C, maximum residence time of 30 min, and maximum purge interval of 8 h; excursions produce black specks in the parison and require barrier extruder shutdown.

    SP482B in Silage Barrier Film: Oxygen Ingress at 85 % RH after 90-Day Field Exposure

    Agricultural silage barrier films with a 75 µm LLDPE/EVA envelope require an oxygen transmission target below 100 cm³/m²·day·atm at 23 °C and 85 % RH to limit aerobic spoilage in the outer silage layer. SP482B is coextruded at a core thickness of 10 µm between two 5 µm LDPE-based tie layers; the outer LLDPE skins are 30 µm each. At 85 % RH, the oxygen transmission rate of the EVOH core increases by a factor of 5–10 relative to 0 % RH conditions, which means a core that measures 2.0 cm³·20 µm/(m²·day·atm) under dry conditions may measure between 10 and 20 cm³·20 µm/(m²·day·atm) when saturated. This moisture-induced barrier loss is measured by preconditioning film samples at 23 °C and 85 % RH for 48 h before oxygen transmission testing per ASTM D3985. The film is produced on a 90 mm three-layer blown film line with a spiral mandrel die at a blow-up ratio of 2.0–2.8 and a frost line height of 600 mm; the EVOH extruder barrel profile is 180 °C to 220 °C. Field exposure trials in wrapped grass silage show that after 90 days, oxygen ingress remains below the target if the outer LLDPE layers are not damaged; punctures larger than 2 mm allow direct moisture ingress and accelerate barrier collapse at the damage boundary. Seal integrity is tested per ASTM F88 and the acid sealant layer must maintain a seal strength above 1.0 N/15 mm after 30 days of outdoor UV exposure. SP482B is not a UV-stabilized grade; therefore, the EVOH core must be fully shielded from direct sunlight by the LLDPE skins, and edge-trim regrind is limited to 10 % to avoid gel speck formation in the barrier layer. Published data for SP482B under silage-specific organic acid exposure is limited; therefore, pre-production trials are required for each silage inoculant formulation.

    Because thermoformed medical device trays require sterile barrier system validation per ISO 11607-1, the 60 µm peelable lidding film is sequenced as PET / LDPE / tie / SP482B / tie / EVA. The EVOH core is set at 10 µm and is coextruded in a chill-roll cast line at a melt temperature of 220 °C; the die exit temperature is 225 °C. Peelable seal strength is generated at 150–170 °C sealing bar temperature, 0.5 s dwell, and 4 bar pressure, yielding 1.0–2.5 N/15 mm seal strength per ASTM F88. The lidding film must maintain these peel forces after EtO sterilization at 54 °C and 70 % RH for 2 h, followed by aeration for 24 h; residual ethylene oxide in the sealed device is controlled below limits specified in ISO 10993-7. The SP482B core is protected from high-moisture sterilization exposure by the PET outer layer and the EVA sealant layer; post-sterilization oxygen transmission is verified by ASTM D3985 at 23 °C and 0 % RH and remains below 5.0 cm³·20 µm/(m²·day·atm) for the film. Because SP482B is a high-ethylene EVOH grade, its oxygen transmission is higher than a 32 mol% grade; the specified 10 µm core is used only when the device shelf life is 24 months and the package is not exposed to prolonged high-humidity storage. Package integrity testing per ASTM F1929 and dye penetration per ASTM F3039 are performed on sealed trays after 7 days at 40 °C and 75 % RH to detect channel leaks at the lid-to-tray interface.

    When SP482B Runs at 8–15 g/10 min Through a 65 mm Grooved-Feed Extruder, LDPE Purging Below 190 °C is Insufficient

    On a 65 mm grooved-feed extruder fitted with a barrier screw and a screen pack of 40/60/100 mesh, SP482B is processed with a barrel profile of 185 °C to 225 °C and a melt pressure of 150–180 bar. The grooved-feed section generates high shear heating; therefore, the first barrel zone above the feed throat must not exceed 185 °C or the melt can exceed 240 °C at the screw tip. Thermal degradation of EVOH produces acetic acid and conjugated polyene discoloration, causing gel particles that appear as fisheyes in cast film. During shutdown, purging with LDPE at 180 °C is insufficient to remove the high-viscosity boundary layer from the screw root; a purge temperature of 205–215 °C and a purge time of 15–20 min are required until the melt pressure stabilizes. The operator monitors melt pressure drift; an increase greater than 5 % over 30 min at constant screw speed indicates accumulation of degraded material in the die adapter. The recommended shutdown sequence is to displace SP482B with LDPE at 210 °C, reduce screw speed to 10 rpm, and then close the die while maintaining barrel temperature for no more than 30 min. When restarting, SP482B is not introduced until the purge LDPE exits the die with no visible yellow discoloration. Gel count testing is performed by casting a 50 µm monolayer film and counting visible defects per 10 cm²; counts above 3 per 10 cm² indicate that the purge was incomplete. Residence time for SP482B in the melt phase should not exceed 30 min; if a downstream die adjustment takes longer, the barrier extruder speed is reduced to 5–10 rpm and the zone temperatures are lowered to 180 °C to limit degradation.

    Anhydrous retinol cream packaged in coextruded PE/EVOH/PE tubes uses a 9 µm SP482B core to limit oxygen ingress that causes retinol oxidation. The product water activity is below 0.5, which keeps the EVOH layer in a low-moisture state and preserves the oxygen barrier at 23 °C and 0 % RH; oxygen transmission through the finished tube is measured per ASTM D3985 and the specification ceiling is 2.0 cm³·20 µm/(m²·day·atm). The tube body is coextruded at 220 °C in a 50 mm three-layer extrusion line, then cut and shoulder-sealed at 260 °C for 0.8 s. Interlayer adhesion between EVOH and PE is provided by a maleic anhydride-grafted PE tie layer of 5 µm; peel strength is tested according to ASTM F904 and remains above 3.0 N/15 mm after 6 months of accelerated aging at 40 °C and 75 % RH. SP482B is not recommended for water-based or ethanol-based cosmetic formulations with free-water activity above 0.7 because moisture absorption plasticizes the vinyl alcohol units and increases oxygen transmission while lowering interfacial adhesion. Published data for SP482B in ethanol-containing cosmetic matrices is limited; therefore, compatibility testing per EU Regulation 10/2011 overall migration below 10 mg/dm² and sensory evaluation after 12 weeks at 40 °C are required before commercial use. The tube packaging line runs at 120 tubes/min; defects associated with the barrier core, such as visible gel specks or layer waviness, are monitored by in-line camera inspection and controlled by keeping the EVOH before processing below 0.04 % residual moisture per ISO 15512.

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    Certification & Compliance
    More Introduction

    EVOH EVAL SP482B is a high-ethylene, sheet-grade ethylene-vinyl alcohol copolymer supplied for coextruded barrier rigid packaging. The product carries a nominal ethylene content of 48 mol%, which places it above standard barrier grades in chain flexibility and drawability while retaining oxygen barrier adequate for oxygen-sensitive contents. Representative supplier property data list a melt flow rate of 2.4 g/10 min at 190°C/2.16 kg according to ISO 1133-1:2022, a density of 1.12 g/cm³ at 23°C according to ISO 1183-1:2019, and a melting point of 163°C by DSC second heating according to ISO 11357-3:2018. These values are representative lot averages published in supplier technical data rather than specification limits. The oxygen transmission rate of a 20 µm cast film at 20°C and 0% RH is typically 1.0 cm³/(m²·day·atm) when measured by ASTM F1927 or ISO 15105-2; the value rises sharply once relative humidity exceeds 60%. Table 1 consolidates the nominal property set.

    PropertyRepresentative valueTest method
    Ethylene content48 mol%Supplier FTIR
    Melt flow rate at 190°C, 2.16 kg2.4 g/10 minISO 1133-1:2022
    Density at 23°C1.12 g/cm³ISO 1183-1:2019
    Melting point, second heating163°CISO 11357-3:2018
    Glass transition temperature58°CISO 11357-2:2020
    Oxygen transmission rate, 20 µm film at 20°C, 0% RH1.0 cm³/(m²·day·atm)ASTM F1927 / ISO 15105-2
    Tensile modulus, machine direction2,200 MPaISO 527-3:2018

    What Differentiates SP482B from Lower-Ethylene EVOH Resins?

    The primary distinction is ethylene content. At 48 mol% ethylene, the crystallinity and intermolecular hydrogen bonding density are lower than in 32 mol% or 38 mol% grades, which lowers oxygen barrier efficiency but increases elongation and flex-crack resistance. The trade-off is expressed numerically: a 32 mol% EVOH grade can reach 0.2–0.4 cm³·20 µm/(m²·day·atm) at 20°C, 0% RH, whereas SP482B typically falls between 0.9 cm³·20 µm/(m²·day·atm) and 1.2 cm³·20 µm/(m²·day·atm) under the same conditions. In a humidity-cycled structure, the relative barrier loss after 300 Gelbo flex cycles according to ASTM F392-23 is smaller for SP482B than for lower-ethylene grades because the more flexible main chain dissipates flexural strain instead of initiating microcracks at barrier-layer corners. Published data for this specific configuration is limited, but production thermoforming trials on PP/EVOH/PP sheet show that corner radii below 2 mm produce visible microcracking with 32 mol% EVOH at draw ratios near 1.4:1, while SP482B retains layer continuity under the same tool geometry.

    The lower melting point relative to 32 mol% grades is another differentiating factor. A 48 mol% ethylene EVOH exhibits a melting point of approximately 163°C, compared with 183–191°C for 32 mol% grades and 171–177°C for 38 mol% grades. This permits barrier-layer melt temperatures in the 200–220°C range without excessive viscosity reduction, but it also narrows the upper processing window because thermal degradation begins more readily above 240°C. Differences from other EVOH products therefore center on the balance between dry-state oxygen barrier and flex-crack resistance; SP482B is not the first-choice barrier layer when the package requires the lowest possible oxygen transmission rate in an unstressed, dry film.

    On production coextrusion sheet lines equipped with 24:1 L/D single-screw barrier extruders and barrier layer outputs between 15 kg/h and 45 kg/h, SP482B is typically pre-dried in dehumidifying hopper dryers to a moisture content below 0.05% at 80°C for 4–6 h, with a supply-air dew point of -40°C. Failure to maintain these drying conditions produces bubble defects at the die lip because residual water hydrolyzes vinyl alcohol groups and reduces molecular weight. Barrel setpoints of 180–210°C, adapter and die setpoints of 210–230°C, and die pressure below 35 MPa are used to avoid excessive residence time. Temperature deviations of ±5°C around a 225°C die setpoint can alter barrier-layer thickness by more than 5% in a feedback-controlled coextrusion line because the viscosity curve steepens above 230°C. The resin is coextruded behind an outer polypropylene or high-impact polystyrene skin using a maleated polyolefin tie layer; direct adhesion to polyolefins without a tie layer is not recommended. If melt temperatures exceed 240°C for more than 4 min, gel particle formation is observed in thermoformed sheet, particularly at die lip edges. During shutdown, the barrier extruder is purged with linear low-density polyethylene and the screw is pulled only after the barrel is below 180°C.

    Regrind of trim from PP/EVOH/PP multilayer sheet can be incorporated into the polypropylene cap or tie layer only if the final recycled content does not exceed 15% by weight and if the granulate is not exposed to moisture above 55% RH. High-ethylene EVOH particles in regrind reduce the melt strength of polypropylene if the reprocessing temperature exceeds 230°C. These are operational boundaries observed on standard sheet lines with 35 mm or 50 mm barrier extruders; they are not product guarantees.

    Regulatory acceptance of EVAL SP482B is governed by the same EVOH copolymer framework as other ethylene-vinyl alcohol grades. In the United States, the resin falls under 21 CFR 177.1360 when used as a component of food-contact articles, subject to end-testing for extractives and end-use limitations in the specific multilayer structure. In the European Union, the ethylene and vinyl alcohol monomers are covered under Regulation (EC) No 1935/2004 and the plastics-specific Regulation (EU) No 10/2011, with overall migration testing conducted according to EN 1186-1:2002 and food simulant assignments per EN 1186-14:2002. The resin is registered under REACH Regulation (EC) No 1907/2006; no SVHC content above 0.1% w/w is declared in the safety data sheet. RoHS Directive 2011/65/EU compliance is generally not relevant for packaging resins but is verified when the multilayer sheet is used in transport packaging for electronic components. Table 2 summarizes the main regulatory references.

    Regulatory frameworkScopeReference or condition
    FDA food contactEVOH copolymers in food packaging21 CFR 177.1360
    EU food contact plasticsOverall migration limit 10 mg/dm²Regulation (EU) No 10/2011
    EU food contact frameworkGeneral safety and inertnessRegulation (EC) No 1935/2004
    REACHRegistered polymer and monomer substancesRegulation (EC) No 1907/2006
    RoHSNo restricted substances above homogeneous material limitsDirective 2011/65/EU

    Thermoformed Barrier Trays and Oxygen Ingress after 300 Gelbo Flex Cycles

    Applications for EVOH EVAL SP482B include coextruded deep-draw trays, cups, and lidding base webs for modified atmosphere packaging of cooked meats, cheese, and oxygen-sensitive concentrates. The grade is selected where the forming step creates high local strain in the EVOH layer, such as rectangular tray corners with draw ratios above 1.2:1 or depths greater than 25 mm. A thermoformed PP/tie/EVOH/tie/PP sheet with a 1.0 mm total thickness and an SP482B layer of 25 µm typically maintains oxygen ingress below 3 cm³/(m²·day·atm) after 300 Gelbo flex cycles when tested according to ASTM F392-23 at 20°C and 50% RH. Lower-ethylene grades can exceed 5 cm³/(m²·day·atm) in the same test because barrier-layer microcracks propagate across the curvature. The exact result depends on tie resin thickness, skin-layer stiffness, and thermoforming plug temperature; published data for this specific configuration is limited.

    Thermoforming trials on a 300 kN clamp-force pressure former with 90°C sheet surface temperature at the forming zone show that SP482B can be drawn to 1.5:1 without visible barrier-layer fracture, whereas 32 mol% EVOH in the same structure develops microcracking at draw ratios above 1.2:1. The wider forming window allows deeper cup geometries and reduces reject rates associated with pinhole formation at the EVOH layer. However, the use of SP482B in retort or sterilized tray formats is constrained by moisture-induced barrier loss; after 121°C retorting for 30 min, the oxygen barrier of the EVOH layer can decline by more than 50% unless a hydrophobic cap layer is maintained below 30 µm and the package is conditioned for at least 7 days at 20°C/50% RH before barrier testing.

    When Relative Humidity Exceeds 65% in Refrigerated Distribution

    At chilled distribution temperatures from 2°C to 5°C, the oxygen barrier of SP482B is influenced more by local moisture content than by temperature. The resin should be positioned as a buried layer between hydrophobic skins; if the central EVOH layer absorbs moisture above 3% by weight, the oxygen transmission rate can rise from 1.0 cm³·20 µm/(m²·day·atm) at 0% RH to above 10 cm³·20 µm/(m²·day·atm) at 90% RH because water molecules disrupt interchain hydrogen bonding. In packaged goods with water activity above 0.95, such as fresh poultry or pasta sauce, the barrier layer must be shielded by at least 150 µm of polypropylene on the food side and 50 µm on the exterior. The exact thickness is governed by target shelf life and the oxygen permeability of the external skin; published data for SP482B at intermediate RH values is limited.

    Incompatibilities include direct contact with high-moisture regrind, long hold-up in hot runners, and melt blending with polyamide or EVOH grades containing high free amine levels. The product should not be combined with amine-based additives or silicones that can catalyze hydrolysis at processing temperatures. If the barrier layer thickness is below 8 µm in a deep-draw application, continuity of the EVOH layer cannot be guaranteed under flexing above 100 Gelbo cycles.