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Anhui Liwei Chemical Co., Limited.

EVOH EW-3201S

    • Product Name: EVOH EW-3201S
    • 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 400834
    Product Name EVOH EW-3201S
    Chemical Name Ethylene-Vinyl Alcohol Copolymer
    Ethylene Content 32 mol%
    Form Translucent Pellets
    Density 1.19 g/cm³
    Melt Flow Rate 190 C 2 16 Kg 1.0 g/10 min
    Melting Point Dsc 183°C
    Glass Transition Temperature 62°C
    Vicat Softening Point 140°C
    Tensile Strength At Break 70 MPa
    Elongation At Break 230%
    Oxygen Transmission Rate 20 C 65 Rh 20 µm Film 0.03 cm³·20µm/(m²·day·atm)
    Moisture Absorption 20 C 65 Rh 2.2 wt%

    As an accredited EVOH EW-3201S factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing EVOH EW-3201S is packaged in 25 kg sealed polyethylene-lined kraft bags, palletized and shrink-wrapped for safe transport.
    Container Loading (20′ FCL) 20′ FCL shipment of EVOH EW-3201S resin, packed in sealed bags on pallets, safely secured for transit.
    Shipping EVOH EW-3201S is a non-hazardous ethylene vinyl alcohol resin. Ship in sealed, moisture-proof bags or containers to prevent water absorption. Avoid direct sunlight and high temperatures. Store in a dry, ventilated area. Standard freight is acceptable, but keep packages upright and protected from physical damage.
    Storage Store EVOH EW-3201S in its original sealed packaging in a cool, dry, well-ventilated area away from direct sunlight, heat sources, and moisture. Keep containers tightly closed to prevent water absorption and contamination. Avoid stacking excessively. Recommended storage temperature is below 30°C. Under proper conditions, shelf life is typically one year from manufacture date.
    Shelf Life For EVOH EW-3201S, shelf life is typically one year in original packaging, stored cool and dry, away from moisture and sunlight.
    Application of EVOH EW-3201S

    On nine-layer blown film lines producing modified-atmosphere poultry bags, EW-3201S is normally positioned as a 3–5 µm core between two maleic anhydride-grafted polyolefin tie layers. The line is operated with a barrier screw of 24:1 L/D and a low-shear Maddock mixing section to limit localized residence time. Melt temperature at the adapter is kept between 190 °C and 220 °C; temperatures above 240 °C accelerate oxidative gel formation and produce black specks at the die lip. Prior to extrusion, the resin is dried at 90 °C for 4 h in a desiccant dryer with a dew point of -40 °C or lower; retained moisture in excess of 0.3% lowers intrinsic viscosity and destabilizes the bubble. The total film gauge is typically 60–90 µm, with the EW-3201S layer representing 3–8% of the structure. Oxygen transmission rate measured according to ASTM D3985 at 23 °C and 0% RH is generally below 1.0 cm³/(m²·day·atm) for fresh films; at 85% RH the OTR increases by one to two orders of magnitude because the hydroxyl-rich EVOH phase is plasticized by sorbed moisture. Converters therefore lock in the dry barrier through desiccant-loaded sealants or high-crystallinity polyolefin skins that limit moisture ingress into the core.

    Regulatory verification for the food-contact film is anchored to 21 CFR 177.1360 or an applicable Food Contact Notification for EW-3201S, and to EU Regulation 10/2011 with migration testing under aqueous, acidic, and fatty simulants specified in the EN 1186 series. The processor must document the functional barrier status of the external polyolefin layers because oxygen barrier cannot be extrapolated from dry cup values alone. Reintroduction of trim scrap containing EW-3201S into polyolefin skin layers is typically limited to 10–15% of the screw feed; higher regrind levels increase interfacial gel defects and cause visible chevron patterns in the film because the EVOH phase elongates into discrete microdomains during the reheating cycle. Direct coextrusion with unneutralized acid-modified tie layers should be avoided; residual free acid at the interface reacts with vinyl alcohol segments and creates carbonized deposits across the die land. The terminal structure is converted into lidding film or side-sealed bags for raw poultry, where the EVOH core suppresses aerobic spoilage without requiring foil lamination.

    RegulationStandard/CodeVerification conditionEW-3201S-specific requirement
    US food contact21 CFR 177.1360 / FCNMigration cellExtraction in 10% ethanol and 95% ethanol food simulants
    EU food contactEU Regulation 10/2011EN 1186 series migrationWorst-case fatty simulant, 60 °C for 2 h or 40 °C for 10 days
    Oxygen barrierASTM D398523 °C, 0% RH and 85% RHReport both dry and humidified values; specify layer thickness
    Interlayer adhesionASTM F904Seal pull at 23 °CFailure must be cohesive in tie layer, not adhesive at EVOH interface

    What Limits Retort Stability in EW-3201S-Based Barrier Trays?

    In polypropylene-based retort trays thermoformed from coextruded sheet, EW-3201S is placed between 5–8 µm tie layers and 50–80 µm PP skins. The sheet is typically produced on a four-extruder cast line with the barrier layer held at 200–220 °C and the PP skins at 230–250 °C; interfacial adhesion is developed in the feedblock before the layer spreads across the coat-hanger die. After thermoforming, the draw ratio in the corner regions can reduce the EVOH layer from a nominal 10 µm to 4–6 µm, creating a barrier weak point that is exposed during retort. Retort sterilization at 121 °C for 30 min with counterpressure of 1.8–2.2 bar drives water into the core. The immediate post-retort oxygen transmission rate can be 5–20× the pre-retort value when measured at 23 °C and 50% RH; partial recovery occurs over 7–14 days as moisture desorbs, but the original dry OTR is not fully restored unless the structure is protected by desiccant-containing cap layers. Sorbed water depresses the dry-state glass transition temperature of the EVOH phase from approximately 60 °C toward or below room temperature, increasing fractional free volume and diffusivity. The resulting barrier shift is not a single-step loss; it reflects time-dependent re-crystallization and moisture redistribution within the confined core.

    ConditionRelative OTR shift vs dry pre-retort baselineMethod
    23 °C, 0% RH, pre-retortbaselineASTM D3985
    23 °C, 85% RH, pre-retort10–100× baselineASTM D3985
    23 °C, 50% RH, 24 h post-retort5–20× baselineASTM D3985
    23 °C, 50% RH, 14 days post-retort2–10× baselineASTM D3985

    The critical processing boundary is the melt temperature/residence time window. EW-3201S must not remain above 230 °C for longer than 10 min; in stagnant zones of the feedblock, thermally degraded EVOH forms crosslinked gels that tear periodically from the interface and deposit on the polishing rolls. Thermal history in the sheet is best controlled by an optimized barrier screw with 22–24:1 L/D and a barrier flight clearance no greater than 0.25 mm. Post-retort delamination at the tie/EVOH interface is evaluated according to ASTM F904, while seal strength before and after sterilization is measured according to ASTM F88/F88M. Published data for EW-3201S in high-temperature retort structures is limited; converter qualification should therefore include instrumented retort trials with oxygen permeation measurement at 48 h and 14 days post-sterilization. Fill-weight and headspace oxygen specifications remain tight because barrier recovery is slower in trays with low headspace volume and high surface-to-volume ratio.

    Fuel Tank Blow Molding Pinch-Off Integrity and Hydrocarbon Permeation

    Six-layer automotive fuel tank blow molding uses an accumulator head to combine high-molecular-weight high-density polyethylene skins, recycled HDPE regrind, two tie layers, and an EW-3201S barrier core. The barrier layer is normally 1–3% of the total parison wall thickness; for a 5 mm tank wall this corresponds to 50–150 µm of EW-3201S. The barrier melt temperature is controlled between 190 °C and 220 °C while the HDPE skins are processed at 210–240 °C. Layer encapsulation is critical at the pinch-off weld where the parison is compressed to form the tank bottom seam. If the EW-3201S core folds or breaks through the outer HDPE layer at the pinch-off, the exposed EVOH edge absorbs fuel and water, swells, and creates a leak path that cannot be corrected by post-mold thermal welding. Continuous parison programming and axisymmetric die geometry are used to maintain uniform barrier distribution around the tank circumference.

    Hydrocarbon permeation is assessed by SAE J1737 or equivalent sealed housing evaporative determination testing under CARB LEV III and EPA protocols. Ethanol-blended fuels increase EVOH plasticization; the barrier factor relative to neat CE10 fuel decreases as the ethanol fraction in contact with the core rises. Published data for EW-3201S in CE10 service is limited, so tank builders qualify the structure by measuring permeation after preconditioning with aggressive fuel mixtures at 40 °C. Scanning acoustic microscopy of cross-sections after tank burst testing is used to identify micro-delamination at the tie/EVOH interface. The operational boundary is moisture: the EVOH layer must remain dry before extrusion and must be protected from post-molding moisture saturation in warehouses; tanks stored at high humidity for more than 30 days before sealed housing testing can show higher permeation values than freshly molded controls.

    When airtight cosmetic tube sleeves are produced on a five-layer sheet line, EW-3201S is placed as a 10–15 µm core between two ethylene-based tie layers and a printable low-density polyethylene outer layer. The sheet is extruded at a total gauge of 250–400 µm, then skived and welded into tube bodies. The EVOH core supplies barrier against oxygen and fragrance loss, but its elongation at break complicates the crimping step if the core is thicker than 20 µm; the crimped seam can develop microcracks that propagate under repeated squeeze cycling. Tube manufacturers therefore reduce the EVOH layer to the minimum thickness that maintains the required oxygen transmission rate, typically measured on the finished sleeve according to ASTM D3985 at 23 °C and 50% RH. Surface treatment of the outer LDPE skin is performed by corona discharge at 38–42 mN/m for flexographic or lithographic print adhesion. The laminate is then joined by hot-air welding at 300–350 °C air temperature; the EVOH layer must be shielded from direct hot-air impingement to avoid local oxidation at the cut edge.

    Batch-to-batch variance in tube line output is frequently traced to interfacial adhesion loss caused by insufficient tie-layer coverage. With a tie-layer thickness below 4 µm, the EW-3201S core can separate from the LDPE during the tube-shoulder compression stage. Processors report that extrusion of EW-3201S at melt temperatures above 225 °C increases gel formation at the feedblock edges, particularly when the line is stopped for more than 15 min. Purging with low-viscosity LDPE before shutdown removes the stagnant EVOH layer from the die and reduces black speck formation on restart. The final tube is used for dermatological creams and high-viscosity cosmeceutical formulations where oxygen-sensitive actives require a non-foil barrier. No specific published data for EW-3201S in cosmetic tube configurations was identified; converter-run flexural and crimp tests are the governing acceptance method.

    For bunker silage covers and silage bags, EW-3201S is coextruded into a five-layer film in which two polyethylene skins protect the barrier layer from condensed moisture and UV stabilizers. The EVOH core is typically 3–5 µm in a 100–150 µm total film. Oxygen transmission rate measured at 23 °C and 50% RH is used as the incoming quality parameter, but the actual silage environment exposes the film to near-saturation humidity and fermentation acids. Under those conditions the EVOH barrier is partially plasticized, and oxygen ingress shifts toward pinholes, abrasion damage, and side-seal defects rather than intrinsic polymer permeation. The functional requirement is therefore not dry-cup OTR alone; pinhole density after installation, side-seal strength per ASTM F88/F88M, and tear propagation after UV exposure per ASTM D1922 are measured on field-aged samples. The EW-3201S layer is not placed as an outer surface because direct contact with silage effluent causes surface crazing and odor pickup. This segment remains a shallow application for EW-3201S because moisture-compromised barrier performance requires thicker EVOH or adjunctive nylon layers only when the film is intended for multi-season use.

    When EW-3201S Is Specified as the Barrier Core in Aseptic Paperboard Packaging

    In gable-top cartons for premium juices and liquid dairy products, EW-3201S can be coextrusion-coated as the core of a three-layer polymer coating on paperboard instead of using aluminum foil. The extrusion coating line operates with a single-screw extruder for the EW-3201S layer at 210–230 °C, while the LDPE sealing layers are extruded at 280–320 °C. The paperboard web is preheated and corona treated before the molten polymer curtain is applied. The barrier layer thickness after draw-down is normally 5–10 µm; at lower thicknesses the coating shows pinholes at exposed paperboard fiber tips, and at higher thicknesses the carton score lines crack more readily during blank folding. Oxygen transmission rate is measured on the flat carton blank and on the folded corners according to ASTM D3985; corner OTR is the more sensitive indicator because barrier thinning at the score line can be 30–50% relative to the flat web.

    Compliance for ambient liquid packaging is verified under EU Regulation 1935/2004 for food contact materials, EU Regulation 10/2011 for plastic layers, and the relevant national BfR recommendations. Since the carton is filled cold or under ultra-clean conditions rather than pressurized retort, moisture-driven barrier loss is slower than in retort trays, but the liquid product still supplies continuous moisture to the inner LDPE layer. The board structure must therefore include a moisture barrier on the product side or use a high-density polyethylene contact layer to slow water transfer into the EVOH core. Published data for EW-3201S in aseptic paperboard configurations is limited; line qualification is performed by measuring oxygen migration into the filled carton over the product shelf life rather than by resin datasheet values alone.

    Pharmaceutical Blister Laminates Require Controlled Cold Forming to Avoid Barrier Layer Thinning

    Cold-formed pharmaceutical blister stock is produced by laminating an EW-3201S-containing barrier film to aluminum foil and a polyvinyl chloride or polypropylene contact web. The EW-3201S film is first coextruded as a 15–30 µm barrier core between tie layers and then cold-rolled into the laminate. During the cold-forming step, the corner geometry creates nonuniform elongation; the EVOH layer thins most at the cavity corners. The depth-to-diameter ratio of the blister cavity is limited to 0.7–1.0 for EVOH-containing laminates because deeper draw causes barrier layer fracture and pinholes. Oxygen transmission is measured according to ASTM D3985, and water vapor transmission is measured according to ASTM F1249; both are reported on the formed cavity, not only on the flat web, because corner thinning governs shelf-life performance for oxygen-sensitive drug formulations.

    The material is qualified under Ph. Eur. 3.1.5 for polyethylene, Ph. Eur. 3.1.3 for polyolefins, and 21 CFR 177.1360 or an applicable Food Contact Notification for the EVOH layer. Hot-melt or solvent-based tie layers used in the laminate must not contain residual primary amines; such species react with vinyl alcohol segments and reduce interlayer adhesion after gamma irradiation or ethylene oxide sterilization. The sterilization dose of 25 kGy can be used if the outer layers contain sufficient radical-scavenging additives, but the EW-3201S layer itself undergoes measurable yellowing above 30 kGy. The terminal structure is a push-through or peel-push blister for hygroscopic actives, where the barrier function depends as much on ultrasonic or heat-seal continuity as on intrinsic EVOH permeability.

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    Certification & Compliance
    More Introduction
    Designation EW-3201S identifies an ethylene-vinyl alcohol copolymer barrier resin of the 32 mol% ethylene class, supplied as pellets for coextruded rigid sheet, thermoformed containers, and cast film. Typical supplier-published values for this class include a melt flow rate of 1.6 g/10 min measured at 210°C under 2160 g load according to ISO 1133-1:2022, a density of 1.19 g/cm³ according to ISO 1183-1:2019, and a melting temperature of 181–185°C by ISO 11357-3:2018. Oxygen transmission rate for a 20 μm film at 20°C and 0% RH is generally reported in the range of 0.3–0.6 cm³·20 μm/(m²·day·atm) under ASTM D3985-17. The resin is not intended for monolayer use; it requires a maleic anhydride-grafted tie layer between the EVOH and polyolefin skins. Ethylene content of 32 mol% places EW-3201S in a class where dry-condition oxygen barrier is higher than 38 mol% or 44 mol% EVOH grades but lower than 29 mol% grades. The trade-off is linked to crystallinity: vinyl alcohol sequences form hydrogen-bonded crystalline domains that obstruct oxygen, while ethylene units disrupt those domains. At 0% RH, oxygen transmission is governed mainly by crystallite volume fraction; at 85% RH, water absorption of 8–12 wt% by ISO 62:2008 plasticizes the amorphous phase and raises permeability by 10–20 fold.

    What limits processing latitude in 32 mol% ethylene EVOH extrusion grades?

    Thermal degradation is the controlling boundary. EVOH releases acetic acid when the melt is held above 230°C; the reaction is self-accelerating and generates gel specks in cast sheet. For EW-3201S, a barrel profile of 180–220°C with adapter and die at 210–230°C is employed on a single-screw barrier extruder with a 30:1 L/D ratio and compression ratio of 2.8:1–3.2:1. The melt temperature upper limit is 230°C, and residence time above that limit should not exceed 20–30 min. At 240°C, gel speck defects become visible in 100 μm sheet after approximately 15 min, and die-lip deposit formation increases. The lower processing limit is set by insufficient melting and layer-thickness fluctuation; melt temperature below 190°C causes wave-like interfacial instability against polypropylene. Pre-drying is mandatory when ambient relative humidity exceeds 60%: desiccant drying at 80–90°C to below 0.3 wt% moisture with a dew point of −40°C or lower is required. Purging sequences must avoid PVC, PVDC, and acetal resins because acidic decomposition products catalyze EVOH degradation; LDPE or a dedicated EVOH purge compound is used before and after the barrier resin. On a 1200 mm wide coextrusion sheet line using a 75 mm primary PP extruder and a 35 mm barrier extruder, EW-3201S is metered as a middle layer at 6 wt% of total sheet structure, with tie-resin layers at 2 wt% each. The barrier extruder runs at 15–20 rpm with melt pressure below 120 bar to maintain a 20–25 μm EVOH core in a 600 μm sheet. Batch-to-batch variation in melt flow rate is normally controlled within ±0.2 g/10 min; moisture regain during handling causes apparent viscosity loss, bubble defects, and wave-like thickness variation in the barrier layer. The sheet is quenched on a three-roll stack at 20–40°C; slow cooling through 160–140°C increases crystallinity but also increases thermoforming stress. Edge-trim regrind containing up to 2% EVOH in PP sheet shows limited haze; above this threshold, scattered EVOH domains become visible in deep-draw cups. Melt rheology data for 32 mol% EVOH with a melt flow rate of 1.6 g/10 min are not uniformly published for EW-3201S. Capillary rheometry per ISO 11443:2021 on this class typically shows apparent shear viscosity in the range of 700–1300 Pa·s at 210°C and 100 s⁻¹, with a power-law index of 0.4–0.6. The viscosity is sensitive to absorbed water; an increase in moisture from 0.1 wt% to 0.3 wt% can reduce apparent viscosity by 20–40%, which is why hopper residence time and dryer dew point are monitored. Published data for this specific configuration is limited; the range is indicative of the ethylene class rather than a stated datasheet value.

    When the barrier layer is moved from 0% RH storage to 85% RH service

    Oxygen permeability of EW-3201S is strongly dependent on relative humidity because water plasticizes the vinyl alcohol segments and reduces crystallinity. Dry-condition oxygen transmission rate at 20°C for 20 μm film is approximately 0.3–0.6 cm³·20 μm/(m²·day·atm) under ASTM D3985-17, but at 85% RH the same gauge can exhibit 5–10 cm³·20 μm/(m²·day·atm); this represents a 10–20 fold increase and is the main reason 32 mol% EVOH is encapsulated between hydrophobic layers. In retort or hot-fill structures, the barrier layer may require a 38–44 mol% EVOH or a blended EVOH/ionomer tie system to retain barrier after 121°C steam processing for 30 min. When EW-3201S is used in high-moisture food packaging, the structure should be designed with a moisture barrier skin such as PP or HDPE and a tie layer of at least 3 μm to limit moisture ingress from the outside and product side. Published data for this specific grade under combined retort and oil-containing food simulants is limited. In coextruded sheet, adhesion of EW-3201S to polyolefin skins is controlled by tie-layer thickness and maleic anhydride availability, not by EVOH moisture content alone. A tie-layer thickness below 3 μm is associated with peel strength below 2 N/15 mm in PP/EVOH laminate tested at 23°C after 24 h conditioning; a tie-layer thickness of 5–8 μm typically maintains peel strength above 4 N/15 mm. Interfacial stability is also viscosity-dependent: if the EVOH/tie-layer viscosity ratio exceeds 3:1 or falls below 0.3:1, zig-zag wave defects can appear at the interface. EW-3201S is formulated to remain within this window against maleic anhydride-grafted PP at 200–220°C, but coextrusion trials with a specific tie resin are required because melt flow rate and maleic anhydride functionality vary among suppliers. Thermoforming of coextruded PP/EVOH/PP sheet produced with EW-3201S requires sheet surface temperatures of 155–170°C and mold temperatures of 20–60°C. The EVOH layer is typically 3–8% of total thickness; below 3%, the layer may rupture during draw ratios above 2.5:1 at the bottom corners of rectangular trays. Above 8%, the barrier layer increases sidewall rigidity and may produce edge cracking when the formed cup is dropped from 1.0 m at 4°C. Plug-assisted forming with oil-free lubrication is specified because hydrocarbon lubricants can reduce interlayer adhesion and produce delamination. Orientation near the EVOH layer after thermoforming changes oxygen transmission at the corner by approximately 1.5–2.5 times versus the flat sheet; corners should therefore be included in barrier validation rather than assuming uniform gauge.

    Comparative Oxygen Ingress Control in Coextruded PP/EVOH/PP Sheet

    Representative supplier-published ranges for EVOH classes are shown in Table 1; EW-3201S corresponds to the 32 mol% class. Exact grade-specific values should be verified against the manufacturer’s certificate of analysis.
    Parameter 29 mol% class EW-3201S / 32 mol% class 38 mol% class 44 mol% class Test method
    Ethylene content 29 mol% 32 mol% 38 mol% 44 mol% Supplier specification
    Melt flow rate 4.0–8.0 g/10 min 1.6 g/10 min 3.0–8.0 g/10 min 3.0–15.0 g/10 min ISO 1133-1:2022, 210°C, 2160 g
    Density 1.21 g/cm³ 1.19 g/cm³ 1.17 g/cm³ 1.14 g/cm³ ISO 1183-1:2019
    Melting temperature 188–193°C 181–185°C 172–178°C 160–166°C ISO 11357-3:2018
    Oxygen transmission rate, 20 μm, 20°C, 0% RH 0.2–0.4 cm³·20 μm/(m²·day·atm) 0.3–0.6 cm³·20 μm/(m²·day·atm) 0.8–1.5 cm³·20 μm/(m²·day·atm) 1.5–2.5 cm³·20 μm/(m²·day·atm) ASTM D3985-17, ISO 15105-2:2023
    Compared with 38 mol% and 44 mol% grades, EW-3201S offers lower dry-condition oxygen transmission and higher barrier per unit thickness, but the processing window narrows and moisture sensitivity increases. Compared with 29 mol% grades, EW-3201S reduces die-pressure variation and allows lower melt temperature during sheet extrusion, at the cost of higher oxygen permeability under dry conditions. In coextrusion coating or biaxially oriented film, high-flow grades above 8 g/10 min are preferred because EW-3201S viscosity may cause poor draw-down or uneven layer distribution at line speeds above 150 m/min. In thermoformed rigid barrier packaging, EW-3201S is selected over high-flow grades because its higher melt strength maintains barrier layer continuity in deep draw ratios up to 3.0:1. For food-contact applications, suitability is governed by EU Regulation No 10/2011 Annex I and Annex II and regional FDA food-contact notification status; the grade is typically supplied with a statement of compliance that specifies overall migration limits and food type restrictions. For materials handled at ambient relative humidity above 60%, pre-drying is required. The resin should not be combined with amine-based additives or transition-metal stearates above 0.1% because these may accelerate gel formation during processing. Published data for the specific interaction of EW-3201S with oxygen-scavenging tie resins is limited; coextrusions containing oxygen-scavenging components must be validated by dynamic oxygen transmission measurement under ASTM F1927-20 or ISO 15105-2:2023 at controlled humidity, not by dry-film coupon values alone. The grade is not recommended for direct contact with acidic fillings above 95°C in monolayer structures because EVOH morphology changes and barrier loss may be irreversible; multilayer encapsulation and tiered testing are required for such conditions.