| HS Code | 849576 |
| Resin Type | Ethylene Vinyl Acetate (EVA) Copolymer |
| Vinyl Acetate Content | 28 wt% |
| Melt Flow Rate | 6 g/10 min (190°C/2.16 kg) |
| Density | 0.955 g/cm³ |
| Melting Point | 73°C |
| Freezing Point | 53°C |
| Vicat Softening Point | 55°C |
| Tensile Strength At Break | 19 MPa |
| Elongation At Break | 750% |
| Hardness | Shore A 84 |
| Brittleness Temperature | -110°C |
| Flexural Modulus | 20 MPa |
As an accredited Elvax 260 EVA Copolymer Resin,Adhesive Grade factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Elvax 260 EVA Copolymer Resin, Adhesive Grade, supplied as pellets in 25 kg multilayer paper bags for safe storage. |
| Container Loading (20′ FCL) | 20′ FCL: Elvax 260 resin (adhesive grade) packed in 25kg bags, palletized, shrink-wrapped, and secured for safe transit. |
| Shipping | Elvax 260 EVA Copolymer Resin (Adhesive Grade) ships as solid pellets in multi-wall paper bags or FIBCs. It is non-hazardous under transport regulations, but avoid dust accumulation, moisture, and excessive heat. Keep dry, store away from ignition sources, and handle with standard industrial hygiene practices. |
| Storage | Store Elvax 260 EVA Copolymer Resin in its original sealed packaging in a cool, dry, well-ventilated area. Keep away from direct sunlight, excessive heat, open flames, and oxidizing agents. Avoid high humidity to prevent clumping or degradation. Maintain moderate ambient temperature and stable conditions; under proper storage, the resin retains its adhesive-grade quality and performance. |
| Shelf Life | Stable for two years from manufacture if stored in original, unopened container in a cool, dry place. |
Compounding of Elvax 260 for case and carton sealing is performed in a 200 L jacketed sigma-blade mixer at shell temperatures between 150 °C and 170 °C. The resin enters the batch as a pelletized base with supplier-reported 28 wt% vinyl acetate content and a melt flow rate of 6 g/10 min at 190 °C under 2.16 kg load per ASTM D1238-20. That low MFR restricts capillary penetration into uncoated recycled kraft linerboard, which is the primary failure mechanism leading to bondline starvation when higher-MFR grades are substituted on high-porosity board. The mixer is charged in a sequence that wets the EVA pellets with liquid rosin ester before wax is added, preventing dry wax agglomeration at the oil jacket interface. Blending under nitrogen with a batch residence time below 45 minutes limits acetic acid evolution from vinyl acetate deacetylation; stainless steel wetted surfaces are standard, and brass or copper fittings are excluded because residual acid accelerates metal ion-promoted ester degradation.
Representative production formulation for this grade uses 30–40 wt% Elvax 260, 35–45 wt% rosin ester tackifier with a ring-and-ball softening point of 95–110 °C, 15–25 wt% Fischer-Tropsch wax, and 0.3–0.8 wt% hindered phenolic antioxidant. The high VA content improves adhesion to polar fibre surfaces, but it also narrows the thermal processing window. At die temperatures above 185 °C, viscosity falls sharply and the molten film penetrates the linerboard, reducing the surface adhesive film available for compression set. At die temperatures below 155 °C, the adhesive does not transfer cleanly from a 1.2 m wide slot-die head, producing edge-thin films and variable open time. Across the die width, a thermocouple variation of more than ±5 °C creates measurable differences in coat weight; thermal uniformity is therefore a production acceptance criterion before adhesive application starts. Open time is not defined by a single ISO/ASTM procedure; production lines determine the compression interval window by running a series of delayed compression trials and measuring fibre tear per ASTM D1876-08(2015)e1 and ISO 11339:2022. Compression bond pressure is maintained at 0.3–0.5 MPa for 5–10 seconds; beyond this range no improvement in bond strength is observed. Release viscosity is determined per ASTM D3236-15 at 170 °C because MFR alone does not predict slot-die transfer behaviour. Published data for continuous vertical twin-screw compounding of this specific grade is limited; batch sigma-blade compounding remains the dominant production route.
| Standard/regulation | Scope | Relevant parameter |
|---|---|---|
| ASTM D1238-20 | Melt flow rate of thermoplastics | 6 g/10 min at 190 °C/2.16 kg |
| ISO 1133-1:2022 | Plastics — determination of melt flow rate | Method A/B melt flow test |
| ASTM D3236-15 | Apparent viscosity of hot melt adhesives | Brookfield Thermosel release viscosity at 170 °C |
| ASTM D1876-08(2015)e1 | T-peel resistance of adhesives | Peel strength after defined conditioning |
| ASTM D903-98(2017) | Peel or stripping strength of adhesive bonds | 180° peel adhesion on flexible substrates |
| FDA 21 CFR 177.1350 | Ethylene-vinyl acetate copolymers for food contact | Extractive limitations by food type |
| REACH SVHC candidate list | Substances of very high concern | 0.1 wt% threshold per article |
Spine gluing of perfect-bound book blocks with Elvax 260 is formulated at 24–32 wt% resin, 38–48 wt% rosin ester, 10–18 wt% paraffin wax, and 0.5–1.0 wt% antioxidant. The MFR of 6 g/10 min at 190 °C under 2.16 kg load, as specified in ISO 1133-1:2022, correlates with high cohesive strength after solidification. Increasing tackifier loading above 48 wt% extends open time but shifts the failure mode from fibre tear to cohesive brittleness at shelf temperatures below 10 °C, as observed under ASTM D1876-08(2015)e1 T-peel conditioning. Reducing tackifier below 38 wt% shortens the wetting window on clay-coated cover stock and increases adhesive failure at the cover hinge.
On a perfect-binding line running at 8,000 books/h, the adhesive is delivered through a spine nozzle at 160–170 °C with a film thickness of 0.4–0.8 mm on the block. Open time on coated paperboard at 23 °C and 50% RH is controlled to less than 60 seconds by adjusting tackifier type and line speed. Because open time lacks a single ISO/ASTM method, quality control uses timed nip-interval trials with page pull strength measured per ISO 11339:2022. The low MFR of Elvax 260 prevents deep migration into the spine fibre, preserving the adhesive film at the block surface where cover bonding occurs. Production lines that raise the application temperature to compensate for viscosity above 180 °C induce bubble entrapment in the nozzle manifold; bubble voids reduce spine flex resistance, and published data for this specific grade under repeated flex testing is limited, so internal flex-rig validation is required before sustained production.
Continuous application to 0.4 mm PVC edge banding on a single-sided edgebanding machine is typically performed through a heated roller coater at 170–185 °C. The hot melt is prepared with 28–35 wt% Elvax 260, 35–45 wt% C5/C9 or rosin ester tackifier, 20–30 wt% paraffin wax, and 0.3–0.6 wt% antioxidant. The roller coater applies a film of 0.08–0.15 mm dry thickness to the band before the pressure roller nips the band onto an MDF panel at 0.3–0.6 MPa. Panel surface temperature at the nip is maintained at 40–55 °C; below 40 °C the high-viscosity melt does not transfer sufficient mass, producing skip lines and low peel strength measured per ASTM D903-98(2017). The open time between roller application and nip must remain below 15–20 seconds because surface skinning on the thin film reduces PVC adhesion. Published data for this specific line-speed/open-time configuration is limited; production verification is required when line speed exceeds 25 m/min.
Substrate moisture in MDF above 8% by mass reduces bond strength under ASTM D903-98(2017) by shifting failure from cohesive in the adhesive film to fibre pull-out in the board surface. This behaviour is measured after conditioning at 23 °C and 50% RH for 24 hours. The 28 wt% vinyl acetate content of Elvax 260 provides polarity for the PVC film, while the 6 g/10 min MFR keeps the molten film in the transfer nip without excessive squeeze-out at the band edge. At application temperatures above 190 °C, visible yellowing of the melt occurs and acetic acid release accelerates deacetylation, especially when the coater reservoir is open to air.
In frozen-food case sealing, the adhesive film must retain cohesion when the board springs back after compression at -20 °C. Elvax 260 is used at 35–45 wt% with a low-glass-transition aliphatic or cycloaliphatic tackifier at 30–40 wt%, microcrystalline wax at 5–15 wt%, and antioxidant at 0.3–0.8 wt%. The higher resin fraction and reduced wax fraction lower the storage modulus at sub-zero temperature, shifting the failure mechanism from brittle cohesive fracture to ductile yielding of the adhesive film. T-peel specimens are conditioned at -20 °C for 24 hours before testing per ASTM D1876-08(2015)e1; a cohesive failure pattern in the adhesive is preferred over adhesive delamination from the linerboard. Corona-treated LDPE film used for frozen-food lamination is specified at 38–42 dyne/cm surface energy; below that range, even 28 wt% VA content does not provide sufficient polar interaction and adhesive peel fails at the film interface.
The processing window narrows because high resin loading raises melt viscosity. A gear-pump melter set at 165–175 °C is required to deliver the adhesive to a slot die without exceeding 180 °C in the heated hose. If the hose temperature exceeds 180 °C, deacetylation releases acetic acid and the melt odour becomes detectable at the coating head. At temperatures below -30 °C, standard EVA-based adhesives may embrittle; published data for this specific grade in multi-layer PE coextrusions below that temperature is limited, and replacement with a lower-Tg polymer or plasticizer addition requires a formal validation plan.
Curtain coating of corrugated board with paraffin wax modified by Elvax 260 at 2–8 wt% resin addition improves adhesion of the wax film to the linerboard and reduces flaking during score folding. The blend is prepared at 120–150 °C in a heated melt tank with low-shear agitation; above 150 °C, wax oxidation darkens the melt and raises acid number, which can destabilise the curtain. EVA content above 10 wt% raises melt viscosity beyond the range suitable for a curtain die, producing film thickness variation greater than ±5% across a 2.5 m web. The EVA fraction does not act as the primary moisture barrier; instead it reduces pinhole formation in the wax film that would otherwise compromise MVTR measured per ISO 15106-2:2005 or ASTM E96/E96M-22b. The modified wax layer is tested for adhesion by a tape snap test after score folding; no single ISO standard applies to the score-fold release of wax from linerboard.
For food-contact corrugated board, the final wax coating must meet applicable requirements for paraffin and EVA components under FDA 21 CFR 177.1350 and FDA 21 CFR 176.170, depending on the board construction and end-use conditions. The low addition level of Elvax 260 in this application does not require pre-drying if pellets are stored below 60% RH; pellets exposed to high humidity should be dried at 60 °C for 2–4 hours to prevent steam-driven pinholes in the curtain. Production lines that set the feed throat above 70 °C report bridging of EVA pellets in the feed hopper; a cooled throat section at 40–50 °C is specified for high-throughput extrusion feeding.
On a profile-wrapping line processing MDF profiles with a 0.20 mm PVC décor film, Elvax 260 is applied through a slotted die onto the film at 150–175 °C before wrapping rollers press the film against the profile. The line speed is usually limited to 12–25 m/min. The limiting factor is not the open time of the melt but the heat transfer through the decorative film to the substrate; if the MDF surface temperature falls below 50 °C, initial tack drops below the threshold needed to prevent spring-back at the profile corners. Peel adhesion of the wrapped profile is tested after 24 hours conditioning at 23 °C and 50% RH per ISO 11339:2022. The adhesive formulation for this segment typically contains 25–35 wt% Elvax 260, 30–42 wt% rosin ester tackifier, 18–28 wt% paraffin or Fischer-Tropsch wax, and 0.3–0.6 wt% antioxidant. Published data for this specific grade on profile-wrapping lines with infrared pre-heat banks is limited; process verification by peel testing of wrap corners is required before sustained production.
The 6 g/10 min MFR is low enough to maintain a continuous film between the slotted die and the nip, preventing droplet breakage at line speed despite the absence of solvent. At the same time, the 28 wt% VA content provides polar adhesion to PVC film and pre-primed MDF surfaces. Clean-up of the die lip must be scheduled every 4–6 hours because recirculated hot melt exposed to air forms a thermally oxidised edge bead that transfers to the wrapped profile as a visible surface defect. Thermal degradation is minimised by maintaining the melting tank under a dry nitrogen purge and by limiting the tank temperature to 170 °C when the line is idle.
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Elvax 260 EVA Copolymer Resin, Adhesive Grade, is a pelletized ethylene–vinyl acetate random copolymer containing a nominal vinyl acetate comonomer level of 28 wt%. Melt mass-flow rate is reported as 6 dg/min under 190°C and 2.16 kg load when tested according to ASTM D1238-20 or ISO 1133-1:2022. Density is approximately 0.955 g/cm³ at 23°C per ASTM D792-20. The grade is positioned for adhesive compounding where higher melt strength than 25 dg/min Elvax 250 and lower melt viscosity than 3 dg/min Elvax 265 are required. In packaging hot-melt assembly, Elvax 260 is typically formulated with rosin ester or hydrogenated hydrocarbon tackifier and paraffin or microcrystalline wax at resin loadings between 30 wt% and 40 wt%. The resin contributes polar adhesion to aluminium, polyester, and corona discharge–treated polyolefin surfaces while retaining sufficient crystallinity for block resistance at warehouse temperatures below 40°C. Unlike EVA copolymers with vinyl acetate content below 18 wt%, the higher comonomer fraction reduces ethylene sequence crystallinity, improves low-temperature flexibility, and permits higher tackifier addition before gross phase separation is observed under 100× phase-contrast microscopy. Melt viscosity is pseudoplastic; the manufacturer does not specify a single-point viscosity for the neat resin, and melt index is used as the controlling rheological parameter. Adhesive specifications therefore reference ASTM D1238 melt index, ASTM D792 density, and, for formulated systems, ASTM E28-99 ring-and-ball softening point, ASTM D1876 peel resistance, or ISO 11339 flexible-adherend peel strength.
Vinyl acetate units disrupt polyethylene crystallites by introducing polar acetate side groups, lowering the crystalline melting endotherm and increasing molecular mobility relative to lower-VA ethylene copolymers. The acetate group participates in dipole–dipole and hydrogen-bond interactions with rosin acid functionality and with metal oxide surfaces; this shifts failure mode from interfacial delamination toward cohesive deformation in formulated hot-melt systems. In adhesive evaluations, compounds containing 35–40 wt% Elvax 260 and a pentaerythritol rosin ester tackifier exhibit cloud-point temperatures above 120°C, indicating a wider homogeneous processing window than equivalent blends with non-hydrogenated C5 tackifier. When peel testing is performed per ASTM D1876 on 50 μm polyester film, the fracture surface must be inspected for residue; clean adhesive transfer from the primary adherend to the secondary adherend confirms cohesive failure rather than interfacial bond deficiency. The higher vinyl acetate content also increases moisture vapour transmission and reduces heat resistance compared with an 18 wt% VA copolymer of equivalent melt index. In formulated adhesives, ring-and-ball softening point may shift downward by 30–40°C relative to low-VA controls. This trade-off must be controlled in applications requiring hot-fill resistance or exposure to 60°C transport conditions. Published neat-resin tensile data are not used as an adhesive specification because peel, shear, and hot-tack values are dominated by tackifier selection, wax crystallinity, and coating weight.
On a corotating twin-screw compounding line with L/D 40:1, barrel zones are typically set from 90°C at the feed throat to 140–150°C at the first mixing zone, with melt temperature at the die maintained between 160°C and 180°C. When Elvax 260 is compounded at screw speeds of 250–350 min⁻¹ and throughputs of 15–25 kg/h on a 25 mm corotating twin-screw extruder, dispersion of rosin ester tackifier is complete within 12 L/D of the first distributive mixing element. Screw speeds below 200 min⁻¹ produce undispersed tackifier agglomerates of 20–50 μm when observed under transmitted light. The upper melt-temperature boundary is set by vinyl acetate degradation. Sustained exposure above 230°C results in elimination of acetic acid, detected as an increase in free acidity from below 2 mg KOH/g to above 5 mg KOH/g by titration of the extrudate. Process equipment must therefore provide stainless steel contact surfaces, atmospheric venting, and a vacuum vent configured below -0.08 MPa gauge if devolatilization is required. Because the resin is supplied with residual moisture typically below 0.1 wt%, a separate predrying step is not required for adhesive compounding when bags are stored at relative humidity below 60%; however, after opening, condensation uptake can occur, and moisture above 0.2 wt% increases hydrolysis of ester groups and batch-to-batch viscosity drift. A desiccant dryer set at 60°C for 4 h with a dew point below -40°C is used on lines where ambient humidity exceeds 70% RH.
Because melt index is inversely related to molecular weight, the 6 dg/min value of Elvax 260 places the material between lower-viscosity Elvax 250 at 25 dg/min and higher-viscosity Elvax 265 at 3 dg/min. In slot-die coating, a hot-melt adhesive formulated with 35 wt% Elvax 260 exhibits a Brookfield viscosity at 175°C that is approximately 4× to 6× the value of an otherwise identical formulation based on Elvax 250; this raises gear-pump back-pressure by 15–25% on pumps rated for 5–10 cm³/rev and requires die heaters to maintain setpoint within ±2°C. Coating grammage control is more stable because the higher melt strength reduces neck-in and edge bead variation on 150–300 mm wide slot dies, but application temperature must be raised by 10–15°C to compensate for viscosity increase. Sprayable construction adhesives using contact nozzle or spiral spray systems require lower-viscosity tackifiers or may blend 10–20 wt% of Elvax 250 or a metallocene polyolefin elastomer to bring application viscosity below 10 Pa·s at 180°C when measured by ASTM D3236-88. If material is held above 200°C for more than 60 min in a heated reservoir, antioxidant consumption accelerates and viscosity drift exceeds ±10%; this is monitored by hourly Brookfield viscosity checks and total acidity measurements per ASTM D974.
| Grade | Vinyl acetate content | Melt index | Density | Processing consequence |
|---|---|---|---|---|
| Elvax 250 | 28 wt% | 25 dg/min | 0.953 g/cm³ | Lower application viscosity; shorter open time; reduced cohesive strength |
| Elvax 260 | 28 wt% | 6 dg/min | 0.955 g/cm³ | Balanced viscosity, hot-tack, and creep resistance; suitable for slot-die control |
| Elvax 265 | 28 wt% | 3 dg/min | 0.955 g/cm³ | Higher melt strength; requires higher processing temperatures |
Values are representative manufacturer technical data. Melt index is determined at 190°C under 2.16 kg load per ASTM D1238; density is determined at 23°C per ASTM D792.
Although the neat resin contains antioxidant stabilisation, adhesive compounding introduces additional exposure to heat, air, and catalytic residues from tackifiers and waxes. The thermo-oxidative induction time of a formulated EVA hot melt is best measured by differential scanning calorimetry under isothermal conditions at 180°C in oxygen per ASTM D3895, and a minimum oxidation induction time of 20 min is often specified for pot-stable assembly adhesives. Hindered phenol antioxidants at 0.5–1.0 wt% extend this induction time, while phosphite synergists at 0.2–0.5 wt% reduce colour formation during extended heating. Avoid contact with copper-containing alloys at processing temperatures above 180°C because copper ions catalyse oxidative degradation and accelerate melt-index drift. High-acid-value tackifiers above 30 mg KOH/g are incompatible with Elvax 260 when processed above 200°C, leading to ester hydrolysis, acetic acid odour, and viscosity loss. Storage in original sealed packaging at temperatures below 40°C and relative humidity below 60% maintains melt-index stability within ±0.5 dg/min for 24 months from production date. Prolonged exposure to ultraviolet light will surface-oxidize the pellets; UV-filtered warehouse lighting or opaque packaging is recommended for long-term storage.
Elvax 260, as a neat ethylene–vinyl acetate copolymer, may be used in food-contact adhesives when the formulated adhesive satisfies the compositional and extractive limits of 21 CFR 177.1350 and, where relevant, EU Regulation No. 10/2011 migration limits for vinyl acetate monomer and total migration. The U.S. regulation does not address the resin alone; compliance is determined on the finished adhesive and the specific food-contact article type. Residual vinyl acetate monomer in Elvax 260 is controlled by the polymerisation process and is typically below 5 ppm when measured by headspace gas chromatography, although lot-specific certificates should be reviewed. Under REACH registration, the copolymer is managed as a polymer substance; no Candidate List entry applies to the polymer itself, but downstream users must evaluate the safety data sheet for residual additives or anti-block agents. RoHS screening of heavy metals by IEC 62321-5 is generally below the 0.1 wt% threshold for lead and mercury, but this is not routinely required for adhesive grades in non-electrical applications. If the adhesive is intended for indirect food-contact packaging under FDA conditions of use A–H, the formulator must test the final formulation for migration because tackifiers, waxes, and antioxidants are typically the limiting components, not the EVA base resin. Published data for this specific formulation configuration is limited and must be verified by end-use migration testing.