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Ethylene-Vinyl Acetate Copolymer EVA 2825-1

    • Product Name: Ethylene-Vinyl Acetate Copolymer EVA 2825-1
    • Factroy Site: Ningdong Energy and Chemical Industry Base, Yinchuan City, Ningxia
    • Price Inquiry: sales4@liwei-chem.com
    • Manufacturer: Ningxia Baofeng Energy Group Co., Ltd
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    Specifications
    HS Code 404734
    Product Name Ethylene-Vinyl Acetate Copolymer EVA 2825-1
    Chemical Family Ethylene-vinyl acetate copolymer
    Vinyl Acetate Content 28 wt%
    Melt Index 25 g/10 min at 190 °C and 2.16 kg
    Density 0.947 g/cm³
    Melting Point 72 °C
    Ring And Ball Softening Point 95 °C
    Vicat Softening Point 48 °C
    Tensile Strength At Break 9 MPa
    Elongation At Break 700%
    Flexural Modulus 20 MPa
    Shore A Hardness 80
    Thermal Degradation Temperature >200 °C
    Physical Form Pellets

    As an accredited Ethylene-Vinyl Acetate Copolymer EVA 2825-1 factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Ethylene-Vinyl Acetate Copolymer EVA 2825-1 is packaged in 25 kg net woven bags with moisture-resistant polyethylene liners.
    Container Loading (20′ FCL) Ethylene-Vinyl Acetate Copolymer EVA 2825-1 loaded in 20′ FCL, dry container, securely stowed, evenly distributed, and protected from moisture.
    Shipping Ethylene-vinyl acetate copolymer EVA 2825-1 is shipped as solid pellets in moisture-resistant bags or containers. It is generally not regulated as dangerous goods for normal transport. Store in a cool, dry, well-ventilated area away from direct sunlight and ignition sources; follow standard industrial hygiene practices. Keep packaging closed and secure during transit.
    Storage Store Ethylene-Vinyl Acetate Copolymer EVA 2825-1 in a cool, dry, well-ventilated area away from direct sunlight, heat sources, ignition sources, and strong oxidizing agents. Keep containers tightly closed and labeled. Protect from moisture and dust; avoid prolonged storage at elevated temperatures to prevent softening or agglomeration. Follow good housekeeping and local regulations.
    Shelf Life Typical shelf life is 24 months when stored in a cool, dry place in original unopened packaging away from sunlight.
    Application of Ethylene-Vinyl Acetate Copolymer EVA 2825-1

    Hot Melt Adhesive Compounding: Viscosity Windows and Tackifier Compatibility

    Within hot melt adhesive compounding lines operating twin-screw extruders at L/D ratios between 40:1 and 48:1, ethylene-vinyl acetate copolymer with a nominal vinyl acetate content of 28 wt% and melt flow index of 25 g/10 min at 190°C/2.16 kg (ISO 1133-1:2022) is introduced as the primary polymer backbone. Pre-drying at 60°C for 2 h is required when storage relative humidity exceeds 60% RH because residual moisture accelerates vinyl acetate hydrolysis at processing temperatures above 170°C and generates acetic acid which corrodes unprotected screw elements. The extruder barrel profile for this grade spans 120°C in the feed throat to 160°C at the strand die, with screw speed maintained between 200 rpm and 350 rpm depending on throughput demand. Prolonged residence time exceeding 30 min at temperatures above 180°C initiates measurable vinyl acetate elimination and a corresponding drop in adhesive peel strength of 15–20% after 8 weeks of accelerated aging at 50°C. Hydrogenated rosin ester tackifiers with ring-and-ball softening points between 85°C and 105°C (ASTM E28-18) are incorporated at loading ratios of 20 wt% to 45 wt% of total formulation mass. The solubility parameter differential between the polymer and tackifier should remain below 1.0 (cal/cm³)⁰·⁵ to prevent phase separation during cooling to ambient temperature. Microcrystalline wax with a congealing point of 75°C to 85°C is added at 5 wt% to 15 wt% to adjust open time and set speed. Paraffin wax incorporation beyond 20 wt% produces a measurable reduction in peel adhesion on HDPE substrates due to wax migration to the bond interface. Brookfield viscometer measurements (ASTM D3236-88) at 175°C yield viscosities between 80,000 mPa·s and 350,000 mPa·s across the tackifier loading gradient. Above 350,000 mPa·s, inadequate wetting of corrugated board substrates is observed on production lines running at conveyor speeds exceeding 30 m/min. Below 80,000 mPa·s, bond strength on PET laminate substrates decreases because cohesive failure of the adhesive layer occurs before substrate fiber tear. End-use bonding applications include spiral-wound paper tube fabrication, case and carton sealing on high-speed packaging lines, and book spine gluing at line speeds of 40 to 60 cycles per minute. For food-contact adjacent packaging, compliance with FDA 21 CFR 175.105 (adhesives) is required, and the antioxidant package must not contain BHT exceeding the specific migration limit of 3 mg/kg under EU Regulation 10/2011. Table 1 presents viscosity and adhesion data across the tackifier loading gradient.
    Tackifier loading (wt%)Brookfield viscosity at 175°C (mPa·s)Peel strength on corrugated board (N/25 mm)Open time (s)
    2080,000–120,00012–158–10
    30150,000–220,00016–2012–15
    40260,000–350,00018–2218–25
    45+>350,00014–16 (decrease)>30

    Published peel strength data for this specific configuration is limited beyond 45 wt% tackifier loading; industrial trials suggest aggregate tackifier—polymer ratio windows should be verified per substrate lot due to variability in surface energy of recycled board stock.

    What Limits Extrusion Cast Film Thickness Control at 28% Vinyl Acetate?

    Extrusion cast adhesive film production with EVA 2825-1 is performed on single-screw extruders with L/D ratios of 30:1 to 36:1, fitted with barrier screws and coat-hanger dies with lip gaps of 0.3 mm to 0.8 mm. The melt temperature at the die exit is controlled within 160°C to 180°C, and chill roll temperatures are maintained at 12°C to 18°C to prevent blocking during winding. Film thickness for adhesives used in textile lamination typically ranges from 30 μm to 80 μm. Thickness gauges employing beta transmission or infrared absorption provide closed-loop feedback to the die lip actuators. Variation exceeding ±5% of nominal thickness across the web width causes uneven bond density in downstream lamination, particularly on polyester and nylon substrates where adhesive penetration depth is limited by tight weave structures. The addition of 0.5 wt% to 1.0 wt% erucamide slip agent reduces blocking on the chill roll but depresses subsequent heat-seal strength by 10–15% because the amide migrates to the film surface and acts as a release agent at the bond interface. For hygienic absorbent product assembly, the cast film is applied between nonwoven polypropylene and polyethylene backsheet at lamination temperatures of 120°C to 140°C under nip pressures of 0.2 MPa to 0.5 MPa. Compliance with REACH Annex XVII entry 50 regarding polycyclic aromatic hydrocarbons is not triggered because EVA does not require extender oils; however, migration testing per DIN EN 1186-1 should be performed when the laminate contacts food simulants. Production-scale failure modes include die-lip buildup of degraded polymer that generates gel particles larger than 50 μm, which are visible as lumps in the adhesive film and produce pinpoint bond voids after lamination. The gel count per square meter should remain below 5 particles larger than 100 μm for pharmaceutical blister lamination applications.The processing window for this grade in cast film is restricted by the low crystallinity inherent to 28% VA content. Melting point measured by DSC (ASTM D3418-21) is typically 62°C to 72°C, which means the film remains tacky at ambient warehouse temperatures above 30°C unless anti-blocking agents are used. Pre-peel forces at 40°C storage conditions increase by 30–40% compared to 25°C storage, which affects automatic unwinding on high-speed converting lines. No published data is available for long-term blocking resistance of this specific grade beyond 6 months of storage at 35°C; users should conduct stacking trials with 500 kg pallet loads before committing to extended inventory.

    Masterbatch Carrier Rheology and Pigment Loading Boundaries

    EVA 2825-1 functions as a pigment and additive carrier resin in masterbatch production where the 25 g/10 min melt flow index enables high filler uptake while maintaining adequate pellet integrity. Color masterbatches formulated with this grade typically incorporate 40 wt% to 60 wt% organic pigments or 60 wt% to 75 wt% inorganic pigments such as titanium dioxide, depending on pigment particle size distribution and surface treatment. The specific energy input during masterbatch extrusion on co-rotating twin-screw extruders ranges from 0.15 kWh/kg to 0.30 kWh/kg, with barrel temperatures of 140°C to 170°C. Screw configurations with kneading block arrangements at 30° and 60° staggering achieve dispersion quality of less than 50 μm agglomerate size as measured by Hegman gauge (ASTM D1210-05). Carbon black masterbatches using this EVA grade as carrier reach loadings of 40 wt% to 50 wt% before viscosity rise exceeds the practical limit of 1,000 Pa·s at 190°C. The end-used polyolefin processing parameters for letdown ratios of 2% to 4% masterbatch in LLDPE film are not affected when the carrier viscosity does not exceed the base resin viscosity by more than 20%. For UV stabilizer masterbatches, hindered amine light stabilizers (HALS) with molecular weights above 1,000 g/mol are compatible, but benzophenone-type UV absorbers can generate color drift if the processing temperature exceeds 160°C for more than 20 min. Storage stability of masterbatches based on this EVA grade is 24 months at 25°C and 50% RH when packaged in moisture-barrier bags; beyond this period, moisture absorption above 0.1 wt% (Karl Fischer titration, ASTM D6304-16) causes surface bloom of additives.For conductive compounds, carbon black loadings of 25 wt% to 35 wt% in EVA 2825-1 carrier yield volume resistivity values of 10² to 10⁴ Ω·cm as measured by ASTM D257-14. These conductive masterbatches are let down into polyethylene at 5 wt% to 10 wt% for electrostatic discharge packaging applications. The operational boundary is defined by the percolation threshold: below 15 wt% carbon black in the final compound, resistivity increases by two to three orders of magnitude, rendering the packaging non-functional for ESD-sensitive electronic components. No published data for this specific EVA grade with single-walled carbon nanotube fillers is available in peer-reviewed literature; users evaluating such systems should conduct percolation curve mapping from 0.5 wt% to 3.0 wt% filler loading.

    When Blown Film Coextrusion Becomes Viable for Adhesive Web Lamination

    Blown film processing of EVA 2825-1 is limited to coextrusion structures where the EVA layer serves as a functional adhesive or sealant layer rather than a structural layer. The low melt strength inherent to 25 g/10 min melt flow index and 28% VA content restricts bubble stability at die diameters exceeding 200 mm unless the layer is coextruded with LDPE or LLDPE as the structural backbone. In a three-layer coextrusion line with die gap of 1.2 mm to 2.0 mm and blow-up ratio of 2.0:1 to 2.5:1, the EVA adhesive layer thickness is maintained at 10% to 20% of total film thickness. Extruder temperatures for the EVA layer are set 10°C to 20°C lower than the polyolefin layers to prevent thermal degradation, with the EVA melt temperature not exceeding 190°C. Frost line height is adjusted to 3 to 4 times the die diameter to accommodate the lower crystallization rate of the high VA content layer. The resulting three-layer film exhibits seal initiation temperatures of 70°C to 80°C, which is 20°C to 30°C lower than that of monolayer LLDPE film, enabling heat-seal operations at reduced energy input on vertical form-fill-seal packaging machines. Seal strength of 15 N/15 mm to 25 N/15 mm is achieved at sealing temperatures of 100°C to 120°C under 0.3 MPa pressure and 0.5 s dwell time (ASTM F88/F88M-21). The adhesive layer also bonds to EVOH barrier layers when a tie resin is not present, although the interlayer adhesion is reduced by 20–30% compared to maleic anhydride-grafted polyolefin tie resins.Operational limitations include gauge variation of ±8% to ±12% in the EVA layer when the total film thickness drops below 40 μm, which impairs seal uniformity on high-speed packaging machines running at 80 cycles per minute or greater. Batch-to-batch variation in VA content of ±1 wt% shifts the seal initiation temperature by approximately 3°C, which must be compensated by real-time seal bar temperature adjustment on automated packaging lines. The blown film route should not be selected for monolayer EVA adhesive webs; cast film extrusion or slot-die coating provides superior thickness uniformity and lower gel formation.In foam extrusion applications, this EVA grade is compounded with azodicarbonamide blowing agent at 2.0 phr to 4.0 phr and dicumyl peroxide crosslinking agent at 0.8 phr to 1.2 phr. The compound is extrusion-foamed on a single-screw extruder with a temperature profile of 105°C to 120°C, which is maintained below the decomposition temperatures of both the blowing agent (195°C to 205°C) and the peroxide (135°C to 145°C, 10 h half-life). The extruded foam sheet is then passed through a continuous hot-air oven at 200°C to 220°C to activate crosslinking and foaming simultaneously. Foam density of 60 kg/m³ to 120 kg/m³ is obtained with compression set values of 25% to 35% after 22 h at 50°C (ASTM D395-18). The high MI of this grade limits foam cell stability; low-density foams below 50 kg/m³ exhibit cell collapse unless 10 wt% to 20 wt% of a higher molecular weight EVA grade (MI below 5 g/10 min) is blended in. Post-foaming shrinkage is controlled by storing foam sheets at 40°C for 24 h before die-cutting. The foam is used in gasket and sealing applications where the softness of 28% VA content provides compression recovery suitable for environmental sealing in appliance and automotive interior components.Polymer modification and blend compatibilization represents another application segment where EVA 2825-1 is added at 5 wt% to 15 wt% to polypropylene and polyethylene compounds. The purpose is impact modification of polypropylene homopolymer for automotive interior trim parts. Notched Izod impact strength (ASTM D256-23) of polypropylene homopolymer increases from 20 J/m to 80–120 J/m when 15 wt% EVA 2825-1 is compounded at 190°C to 210°C. The dispersed EVA phase typically exhibits particle sizes of 0.5 μm to 2.0 μm as observed by scanning electron microscopy on cryofractured surfaces. Below 5 wt% loading, particle coalescence is insufficient to achieve meaningful impact improvement. Above 15 wt%, tensile strength of the compound drops by more than 20% relative to the base polypropylene. The compound is processed on twin-screw compounding lines and pelletized for subsequent injection molding operations. Injection molding of impact-modified polypropylene containing EVA 2825-1 is performed at melt temperatures of 210°C to 230°C and mold temperatures of 30°C to 50°C. The EVA phase does not contribute significantly to warpage because the shrinkage differential between the matrix and the dispersed phase is relatively low. For recycled polyolefin streams, 5 wt% EVA 2825-1 acts as a compatibility enhancer for mixed polyethylene-polypropylene fractions, improving the elongation at break from 50% to 150–200% when the recycled blend contains 20% polypropylene contamination. No published data is available for the long-term thermo-oxidative stability of these recycled blends beyond 12 months of outdoor exposure; users must incorporate 0.1 wt% to 0.2 wt% of a secondary antioxidant blend based on phosphite and thioester chemistry.Wire and cable filler compounds constitute a peripheral application for this grade. The high melt flow index limits use in primary insulation applications where heat deformation resistance per UL 1581 is required. However, filler compounds for low-voltage cable bedding and jacketing filler layers incorporate EVA 2825-1 at 20 wt% to 30 wt% with calcium carbonate or aluminum trihydrate loadings of 150 phr to 200 phr. The resulting compound has a limiting oxygen index of 24% to 28% when ATH is used at 200 phr, measured per ASTM D2863-19. Extrusion of these filler compounds on single-screw extruders at L/D 24:1 to 30:1 with barrel temperatures of 120°C to 150°C is stable provided the compound moisture content is below 0.1%. The operational boundary for this grade in wire and cable is defined by the upper service temperature of 70°C. Beyond this temperature, the heat deformation test per IEC 60811-508 shows penetration exceeding 50% within 4 h. Compounds requiring service above 90°C should select EVA grades with VA content below 20% or move to crosslinked systems with triallyl cyanurate coagent.Adhesive web production for nonwoven hygiene products uses EVA 2825-1 in slot-die coating operations. A pre-melted reservoir at 150°C to 165°C is fed to a positive displacement gear pump delivering 15 g/m² to 50 g/m² coating weights onto release paper or direct onto nonwoven substrates. Viscosity stability at 160°C is maintained for 8 h with less than 5% drift when 0.5 wt% of a hindered phenolic antioxidant (Irganox 1010 equivalent) and 0.3 wt% of a phosphite secondary antioxidant are incorporated. Without the secondary antioxidant, viscosity drift of 15–20% is observed over 8 h due to chain scission and subsequent crosslinking. Coating line speeds range from 50 m/min to 200 m/min. At speeds exceeding 150 m/min, the coating weight uniformity degrades beyond ±10% due to inadequate re-melt capacity of the inline melt tank. The adhesive web is used for disposable diaper elastic attachment, adult incontinence pad fixation, and feminine hygiene product assembly. In contrast to hot melt adhesives applied by spiral spray nozzles, the pre-formed adhesive web eliminates the risk of airborne adhesive particles contaminating surrounding manufacturing equipment.The final application segment addresses the use of EVA 2825-1 in low-temperature flexible sheeting and waterproofing membranes. The compound incorporates 100 phr EVA, 30 phr to 50 phr dioctyl adipate or diisononyl phthalate plasticizer, 5 phr to 10 phr epoxidized soybean oil as co-stabilizer, and 2 phr to 4 phr calcium-zinc heat stabilizer. The formulation is calendered to sheet thicknesses of 0.5 mm to 2.0 mm at roll temperatures of 130°C to 150°C. The resulting sheeting exhibits Shore A hardness of 55 to 65 (ASTM D2240-15) and a brittle point below -40°C (ASTM D746-20). Tensile strength of 5 MPa to 8 MPa and elongation at break of 700% to 900% (ASTM D638-14) are typical for this grade when plasticized at 30 phr. The sheeting is used for pond liners, tunnel waterproofing membranes, and containment applications where cold-temperature flexibility is required. The operational limitation for plasticized EVA sheeting is plasticizer migration: at 40 phr DOP loading, plasticizer loss of 5% to 8% over 12 months at 25°C occurs when the sheeting contacts asphalt or bitumen substrates. In such configurations, EVA grades with higher molecular weight and lower MI are preferred to reduce free-volume-driven plasticizer diffusion.
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    Certification & Compliance
    More Introduction

    Ethylene-vinyl acetate copolymer EVA 2825-1 is a random copolymer with a nominal vinyl acetate content of 28 wt% and a melt flow rate of 25 g/10 min determined at 190°C under 2.16 kg load according to ISO 1133-1:2022 or ASTM D1238. The nominal density is 0.950 g/cm³ by ISO 1183-1. The material is supplied as translucent pellets and falls under CAS registry number 24937-78-8. The 28 wt% vinyl acetate content reduces polyethylene crystallinity, lowering the melting peak to approximately 73°C by ASTM D3418 and increasing polarity, adhesion to polar substrates, low-temperature flexibility, and compatibility with tackifier resins relative to lower-vinyl-acetate copolymers.

    Specification profile and test methods

    Batch certificates of analysis govern release values, but representative grade-selection data are listed in the following table. Values are not dual-specification limits unless separately identified in a purchase agreement.

    PropertyRepresentative valueTest method
    Vinyl acetate content28 wt%ASTM D5594
    Melt flow rate25 g/10 min at 190°C, 2.16 kgISO 1133-1:2022, ASTM D1238
    Density0.950 g/cm³ISO 1183-1
    Melting peak73 °CASTM D3418
    Vicat softening temperature46 °CASTM D1525
    Shore A hardness80ISO 868
    Tensile strength at break10 MPaASTM D638-14
    Elongation at break800%ASTM D638-14
    Flexural modulus18 MPaISO 178

    Melt viscosity for this grade is lower than that of EVA copolymers with equivalent vinyl acetate content but lower melt flow rate. Viscosity should be measured for each formulation because fillers, tackifiers, and waxes shift the high-shear flow curve independently of neat-resin melt flow rate. Incoming lots can be screened by melt flow ratio at 190°C using 2.16 kg and 10 kg loads; variation in vinyl acetate content above 1 wt% can shift melt viscosity and should trigger formulation adjustment.

    What Distinguishes 28 wt% Vinyl-Acetate Copolymer from Lower Vinyl-Acetate Grades?

    The higher vinyl acetate content in EVA 2825-1 produces greater polarity and chain irregularity than EVA grades containing 14 wt% or 18 wt% vinyl acetate. This increases adhesion to aluminum foil, polyester film, polyvinyl chloride, paper, and polar nonwoven substrates, but reduces tensile strength and thermal stability relative to lower-VA copolymers. The lower crystalline fraction also depresses heat-seal initiation temperature and improves toughness at freezer temperatures. Compared with high-VA elastomers exceeding 40 wt% vinyl acetate, EVA 2825-1 retains higher tensile strength, lower surface blocking, and easier pellet feeding in gravimetric dosing equipment.

    In extrusion lamination, the 25 g/10 min melt flow rate reduces backpressure and permits lower melt temperatures, but the same flow characteristic reduces melt strength and increases neck-in at slot dies relative to grades with melt flow rates below 10 g/10 min. The operational boundary is most visible on chill-roll lines: die gap and air-gap settings must be optimized to control draw resonance, and melt temperature should remain within ±5°C of the set point to prevent viscosity drift at the die lip.

    Thermal-oxidative stability limits during compounding and coating

    EVA 2825-1 should be processed with barrel set temperatures between 150°C and 190°C in the feed zone and 190°C to 210°C at the die, with melt temperature kept below 210°C as measured by infrared thermometry at the die exit. Sustained operation above 230°C accelerates deacetylation, releasing acetic acid that corrodes exposed steel surfaces and generates gel particles. When a 75 mm co-rotating twin-screw extruder with L/D 32:1 is used, side-feed addition of fillers after plastication reduces localized shear heating; a vacuum vent at -0.08 MPa assists volatile removal. Melt pressure differential across a screen pack should be recorded. An increase beyond 20 bar from the clean-screen baseline signals gel accumulation or filler dispersion breakdown, and the screen pack should be changed.

    Pre-drying is required when resin has been stored at relative humidity above 60%. Drying at 60°C for 4 h in a dehumidified hopper dryer reduces surface defects in profile extrusion, extrusion coating, and cast film. Pellet softening near 55°C requires feed-zone cooling water to be maintained at or below 30°C to prevent pellet bridging in the feed throat. The polymer is incompatible with strong oxidizing acids and with halogenated flame-retardant systems that release acidic species at processing temperatures. Peroxide crosslinking is possible when dicumyl peroxide or similar initiators are added, but the resulting vulcanization kinetics depend strongly on mixing temperature; the compound should remain below the peroxide decomposition threshold during compounding to avoid premature gelation.

    In hot-melt adhesive compounding, EVA 2825-1 is dry-blended with hydrogenated rosin ester or C5/C9 hydrocarbon resins at resin loadings of 30 wt% to 50 wt% and paraffin or Fischer-Tropsch wax at 10 wt% to 20 wt%. The mixture is processed in high-shear mixers or twin-screw extruders at 160°C to 180°C. Brookfield viscosity at 180°C according to ASTM D3236 is formulation-dependent; the neat resin melt flow rate does not predict hot-melt viscosity after tackifier dilution. Open time and set time are controlled by wax crystallinity and resin glass transition rather than by EVA grade alone. The 28 wt% vinyl acetate content improves specific adhesion to polar films, but reduces heat resistance relative to EVA grades with 18 wt% vinyl acetate and similar melt flow rate. Therefore, EVA 2825-1 is selected for low-application-temperature adhesives, packaging assembly, and bookbinding where substrate wetting and flexibility are more critical than sustained load-bearing temperature.

    In extrusion coating and blown film sealant layers, EVA 2825-1 is used as the heat-seal layer in coextruded structures because the 28 wt% vinyl acetate content lowers seal initiation temperature and broadens the seal window on high-speed form-fill-seal equipment. Chill-roll temperatures between 15°C and 20°C reduce blocking of the low-hardness surface. Corona treatment is often applied after extrusion to raise surface energy for laminating adhesives and printing inks. In solvent-borne coating, EVA 2825-1 dissolves in aromatic hydrocarbon and chlorinated solvent systems at elevated temperatures. Toluene solutions at 25 wt% solids require heated mixing at 60°C to 70°C; gel formation occurs if polymer is added too rapidly to under-agitated solvent or if the solution is overheated above 80°C.

    Comparative property matrix across EVA 2825-1 and reference polyolefins

    The following comparative values are representative and are provided for grade-selection contrast. Lot-specific certificates of analysis control release.

    PropertyEVA 2825-1EVA 18% VA, MFR 15LDPE, MFR 7
    Vinyl acetate content28 wt%18 wt%0 wt%
    Melt flow rate25 g/10 min15 g/10 min7 g/10 min
    Density0.950 g/cm³0.940 g/cm³0.919 g/cm³
    Melting peak73 °C86 °C110 °C
    Shore A hardness809096
    Tensile strength at break10 MPa15 MPa20 MPa
    Elongation at break800%700%600%

    The property matrix indicates that EVA 2825-1 trades tensile strength and heat resistance for lower processing temperature, higher elongation, and greater surface polarity. The lower melting peak and lower Shore A hardness support adhesion to irregular paper and film substrates, while the higher melt flow rate reduces melt viscosity for roll coating and sprayable hot-melt systems. The same attributes make the grade unsuitable for applications requiring high creep resistance at temperatures above 50°C unless the formulation is crosslinked or blended with a higher-melting polymer.

    Regulatory status is application-dependent. For food-contact use, FDA 21 CFR 177.1350 covers ethylene-vinyl acetate copolymers, provided the antioxidant and processing-aid package also meets applicable positive-list requirements. EU compliance must be assessed under Regulation (EC) No 1907/2006 for REACH registration and under Directive 2011/65/EU for RoHS restricted substances in electrical and electronic equipment. Suppliers should provide lot-specific declarations for heavy metals, polycyclic aromatic hydrocarbons, and residual monomers. The user is responsible for verifying that the final compounded product, including tackifiers, waxes, fillers, and colorants, remains within the appropriate migration or extractables limits for the intended market.

    In filled compounds, calcium carbonate or talc loadings above 30 wt% increase viscosity and reduce elongation, but improve modulus and lower formulation cost. Compounding on a 50 mm twin-screw extruder with L/D 40:1 and atmospheric venting can disperse hydrophobic-coated calcium carbonate at loads up to 50 wt%, but melt temperature must be monitored because filler-induced viscous heating can push the melt above the 210°C stability limit. Batch-to-batch filler moisture should be controlled below 0.2 wt% before side-feeding; otherwise vacuum venting may not remove sufficient moisture and surface porosity appears in extruded profiles. In such filled systems, EVA 2825-1 is typically compared with ethylene-octene copolymers rather than standard EVA grades because the high acetate content and high melt flow provide comparable flexibility at lower cost but with reduced thermal-oxidative stability. Published data for specific filled configurations are limited, so pilot-scale trials remain necessary before production commitment.