| HS Code | 710370 |
| Product Name | EVAtech 160I/21 |
| Material Type | Ethylene Vinyl Acetate (EVA) Copolymer Compound |
| Grade | Crosslinkable Foam Grade |
| Vinyl Acetate Content | 16% |
| Density | 0.930 g/cm³ |
| Melt Flow Rate | 2.1 g/10 min at 190°C/2.16 kg |
| Melting Point | 85°C |
| Tensile Strength | 20 MPa |
| Elongation At Break | 700% |
| Hardness | 90 Shore A |
| Crosslinking Type | Peroxide Crosslinkable |
| Foam Cell Structure | Fine and Uniform |
| Foam Expansion Ratio | High Expansion Capability |
| Vicat Softening Temperature | 70°C |
| Brittleness Temperature | -70°C |
| Processing Method | Injection Molding, Extrusion, Compression Molding |
As an accredited EVAtech 160I/21 EVA Copolymer Compound,Crosslinkable Foam Grade factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Supplied as free-flowing pellets in 25 kg polyethylene bags, palletized and stretch-wrapped for safe handling and storage. |
| Container Loading (20′ FCL) | 20′ FCL loading: EVAtech 160I/21 EVA copolymer compound packed in palletized cartons, secured and containerized for safe transport. |
| Shipping | Ship as non-hazardous polymer pellets in sealed 25 kg bags, palletized and stretch-wrapped. Protect from moisture, heat, and direct sunlight during transit. Use dry, clean containers with adequate ventilation. Avoid prolonged storage above 30°C. Ensure secure stacking to prevent bag damage and maintain product integrity. |
| Storage | Store in a cool, dry, well-ventilated area, away from direct sunlight, heat sources, and open flames. Keep containers tightly sealed to prevent moisture absorption and contamination. Maintain temperatures below 30°C to avoid premature crosslinking. Use within the manufacturer’s specified shelf life, typically 6–12 months from production date. |
| Shelf Life | Shelf life is typically twelve months from manufacture if stored unopened in original packaging in cool, dry conditions. |
EVAtech 160I/21, with a nominal vinyl acetate content of 16 wt% and a melt flow index of 2.1 g/10 min under ISO 1133-1:2022 conditions, is dry-blended at 100 phr with 3.0–4.0 phr azodicarbonamide, 0.9–1.2 phr dicumyl peroxide, 1.0–2.0 phr zinc oxide, 0.5–1.0 phr zinc stearate, and 5–15 phr calcium carbonate for chemically crosslinked footwear midsole stock. Mixing is performed in an internal mixer with a 75 L net chamber volume at rotor speed 35–40 rpm; the drop temperature is controlled between 115°C and 120°C because peroxide scavenging accelerates sharply above 125°C. The discharged batch is sheeted on a two-roll mill at 100–110°C with a nip gap of 1.5–3.0 mm and then cooled to 40–50°C before preform cutting. Molding is executed in a multi-platen compression press at 165–172°C for 10–14 min under 4–6 MPa; the functional processing window is approximately ±5°C because the dicumyl peroxide half-life at 170°C is close to 1 min, while zinc oxide-activated azodicarbonamide decomposition onset is depressed into the 155–165°C range. If crosslink density develops before sufficient gas liberation, expansion stalls above target density; if gas evolution outpaces melt strength, cell coalescence and split voids appear. Midsole foam density is controlled at 180–220 kg/m³, with Asker C hardness of 48–55, compression set below 30% after 6 h at 50°C under 25% deflection per ASTM D395-18 Method B, and tensile strength above 2.0 MPa when tested per ASTM D3575-20 Suffix T. Terminal products include die-cut midsoles, full-length wedge soles, molded sock liners, and heel inserts. Footwear components exported to the EU are normally screened for dimethyl fumarate under EU 2009/251/EC, REACH Annex XVII restrictions, and AFIRM RSL limits for extractable heavy metals, phthalates, and polycyclic aromatic hydrocarbons. Amine-based additives and sulfur donors must be excluded from regrind streams because they scavenge peroxide radicals and depress cure efficiency. Packed cartons should not be stored above 50°C to avoid permanent indentation and density gradients in finished midsoles.
For thermally insulating pipe sleeves and HVAC duct liner, EVAtech 160I/21 is formulated at substantially higher blowing-agent loading because the target density is far below footwear-grade foam. A starting-point formulation uses 100 phr compound, 12–16 phr azodicarbonamide, 0.6–0.8 phr dicumyl peroxide, 1.0–2.0 phr zinc oxide, 1.0–2.5 phr zinc stearate, and 10–30 phr magnesium hydroxide or aluminium trihydroxide where flame-retardant classification is required. The batch is fed to a single-screw extruder with L/D 24:1 and a screw compression ratio of 1:2.5; barrel temperatures are held at 95–115°C from feed throat to metering zone, while the die head is maintained at 105–120°C to prevent premature blowing inside the screw channel. The extrudate enters a continuous hot-air vulcanization oven at 190–230°C with line speed between 3 m/min and 8 m/min, where peroxide crosslinking and azodicarbonamide decomposition proceed simultaneously. The critical threshold is blowing-agent dosage: below 4 phr, density rises above 45 kg/m³ and thermal conductivity exceeds 0.042 W/(m·K); above 18 phr, cell walls rupture, closed-cell content drops below 90%, and visible internal fissures form. Target foam properties for pipe insulation are density 25–35 kg/m³, thermal conductivity 0.036–0.040 W/(m·K) at 25°C per ASTM C518-21, water vapour transmission below 0.10 perm·inch per ASTM E96/E96M-21, and water absorption by volume below 1% after 24 h immersion per ASTM D1056-20. The expanded sleeves, sheets, and duct liner are cut in thicknesses from 6 mm to 50 mm, often with acrylic adhesive backing applied after corona treatment to 38–40 dyn/cm surface energy. Compliance for chilled-water and HVAC service commonly references ASTM C534/C534M-23 for elastomeric cellular insulation and local building-code smoke and flame indexes. The main production bottleneck is oven temperature stratification: a cross-web temperature drop greater than 10°C creates a dense skin and low-density core, which increases post-compression thickness loss under insulation cladding.
Because automotive interior laminates require a thermoformable closed-cell core, EVAtech 160I/21 is calendered into rollstock with target density 45–70 kg/m³ and thickness 2–6 mm. A production-start formulation uses 100 phr compound, 4.5–7.0 phr azodicarbonamide, 0.8–1.1 phr dicumyl peroxide, 0.5–1.0 phr zinc oxide, 0.5–1.0 phr zinc stearate, and 1–3 phr color masterbatch. Calendering is run on a four-roll inverted-L calender with roll temperatures of 100–115°C; the final nip gap is matched to the calculated green-sheet thickness required for the expansion ratio. The sheet is then expanded in a rotocure oven at 170–190°C, followed by a post-cure tunnel at 80°C for 24 h to strip residual acetaldehyde and azodicarbonamide decomposition odor. Lamination to polyester, polypropylene nonwoven, or PVC facing is performed at 130–150°C with nip pressure of 0.5–1.0 MPa. The foam surface is embossed in-line to improve drape and reduce delamination on contoured door-panel substrates. The key process boundary is thermoformability: the crosslinked foam must soften between 120°C and 140°C without melting or shrinking more than 2% after forming. High crosslink density locks the cell structure and prevents deep-draw door-panel contours, while insufficient crosslink density permits cell collapse in the forming tool. Flammability is measured per FMVSS 302 or ISO 3795:1989/Amd 1:2016; the horizontal burn rate must not exceed 100 mm/min for automotive interior panels. Tensile strength above 0.3 MPa and elongation above 120% per ASTM D3575-20 Suffix T are commonly specified. Emission testing is referenced to VDA 278 or equivalent OEM methods when the rollstock is destined for passenger-compartment parts. Terminal products include die-cut headliner pads, door-panel cushion layers, dashboard crash-pad backing, parcel shelf liners, and HVAC blend-door seals. Compliance with REACH Annex XVII and the EU End-of-Life Vehicle Directive 2000/53/EC is relevant for EU-trimmed vehicles, and the compounded rollstock must be free from polybrominated diphenyl ethers for RoHS 2011/65/EU Annex II where applicable.
| Application | ADCA loading | DCP loading | Target density | Key measured property |
| Footwear midsole | 3.0–4.0 phr | 0.9–1.2 phr | 180–220 kg/m³ | Compression set <30% per ASTM D395-18 |
| Pipe insulation | 12–16 phr | 0.6–0.8 phr | 25–35 kg/m³ | Thermal conductivity 0.036–0.040 W/(m·K) per ASTM C518-21 |
| Automotive rollstock | 4.5–7.0 phr | 0.8–1.1 phr | 45–70 kg/m³ | Burn rate <100 mm/min per FMVSS 302 |
| Appliance gasket | 2.0–3.5 phr | 0.7–1.0 phr | 120–180 kg/m³ | Compression set <30% per ASTM D1056-20 |
| Sports matting | 5.0–8.0 phr | 0.8–1.2 phr | 50–70 kg/m³ | Tear strength >1.5 N/mm per ASTM D624 |
| Marine buoyancy | 6–9 phr | 0.6–0.9 phr | 35–55 kg/m³ | Water absorption <1 vol% per ISO 2896:2001 |
Compression-set resistance in appliance gasket foam is governed by crosslink density and closed-cell geometry rather than bulk polymer hardness alone. For refrigerator door seals, HVAC access-panel gaskets, and air-filter frame seals, EVAtech 160I/21 is compounded with 100 phr polymer, 2.0–3.5 phr azodicarbonamide, 0.7–1.0 phr dicumyl peroxide, 0.5–1.0 phr zinc oxide, 0.3–0.8 phr zinc stearate, and 15–30 phr calcium carbonate or talc where dimensional stability is required. Mixing is conducted below 120°C to avoid scorch; the sheet is compression molded at 165–175°C under 3–5 MPa and then die-cut into gasket profiles. Target density is 120–180 kg/m³, firmness is usually in the Shore A 15–25 range when measured per ASTM D2240-15, and compression set after 22 h at 70°C under 25% deflection is held below 30% per ASTM D1056-20. The processing boundary is narrow: increasing dicumyl peroxide beyond 1.1 phr drives compression set below 20% but raises hardness above Shore A 30, producing closure force that exceeds refrigerator door-seal magnet pull and creates gapping in low-temperature service. Reducing peroxide below 0.6 phr leaves uncrosslinked domains that creep under repeated door-slam loading. Water absorption by weight should remain below 5% after 24 h immersion, and closed-cell content above 85% is required to prevent condensate uptake during freezer defrost cycles. Flame classification is frequently requested as UL 94 HF-1 on the final gasket profile. Because appliance gaskets must survive repeated compression at low temperatures, the foam is conditioned at -20°C for 4 h before compression testing to check cell-wall embrittlement. Terminal products include magnetic refrigerator door gaskets, HVAC panel seals, air-conditioner filter seals, and appliance access covers.
In fitness mat production, the calendered preform is expanded in a multi-opening press to produce sheet stock with density 50–70 kg/m³, tensile strength above 0.25 MPa, elongation above 150%, and tear strength above 1.5 N/mm per ASTM D624-00(2020) Die C. The starting formulation for EVAtech 160I/21 uses 100 phr compound, 5.0–8.0 phr azodicarbonamide, 0.8–1.2 phr dicumyl peroxide, 1.0–1.5 phr zinc oxide, 0.5–1.0 phr zinc stearate, and 10–20 phr calcium carbonate. Mixing is performed in a Banbury internal mixer at 35–40 rpm; the batch is dropped at 115–120°C and sheeted through a two-roll mill at 100–110°C. The preform is then crosslinked and expanded in a hydraulic press at 170–180°C for 12–18 min, with pressure released in a controlled step to prevent post-expansion shrinkage. The production conflict is the requirement for high tear strength in thin 8–15 mm mat stock without excessive density from overcrosslinking; increasing peroxide beyond 1.4 phr improves tear strength but pushes density above 75 kg/m³ and reduces perceived cushioning. For childcare and yoga products, compliance with EN 71-3:2019+A1:2021 migration limits for soluble elements is tested on the final mat, and REACH candidate-list screening is required for EU import. Gym flooring applications may specify surface resistivity below 10⁹ Ω per IEC 61340-2-3 only when antistatic carbon black is added; the base foam is not intrinsically antistatic. Terminal products include yoga mats, gymnastics landing mats, fitness mats, mobility pads, and die-cut protective floor tiles for martial arts studios.
Pre-drying at 60°C for 2 h is applied when storage humidity exceeds 60% because moisture accelerates azodicarbonamide decomposition before the melt reaches full crosslink temperature and creates open porosity. For marine buoyancy inserts and fender pads, EVAtech 160I/21 is compounded with 100 phr polymer, 6–9 phr azodicarbonamide, 0.6–0.9 phr dicumyl peroxide, 1.0–1.5 phr zinc oxide, and 0.5–1.0 phr zinc stearate. The compound is extruded into rod or sheet profile and expanded in a heated mold at 170–180°C, then cooled under 0.3–0.5 MPa to stabilize cell dimensions. Target density is 35–55 kg/m³, closed-cell content above 90% when measured by gas displacement per ASTM D6226-21, and water absorption below 1 vol% after 7 days immersion per ISO 2896:2001. If the molding temperature falls below the azodicarbonamide decomposition window or blowing-agent dispersion is poor, closed-cell content drops below 90%, water uptake increases beyond 5 vol% after repeated compression cycles, and buoyancy retention in service is reduced below the design margin. Buoyancy aids using such foam are generally tested to ISO 12402-5 for personal flotation devices or ISO 12402-7 for materials and components, but the foam alone does not constitute a certified device without the full garment assembly and approval. Terminal products include foam inserts for life jackets, buoyancy blocks for floating cables, dock fender cores, aquatic therapy kickboards, and impact-absorbing hull gaskets. Mixing equipment must be thoroughly purged when switching from EPDM formulations because sulfur donors and amines depress peroxide efficiency and create surface tack in the final foam.
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EVAtech 160I/21 EVA Copolymer Compound, Crosslinkable Foam Grade, is supplied as a pelletized ethylene-vinyl acetate copolymer formulation for chemically blown, peroxide-crosslinked closed-cell foam conversion. The grade designation corresponds to a nominal vinyl acetate content of 16 wt% and a melt flow rate of 2.1 g/10 min; the specification window is typically 15.0–17.0 wt% vinyl acetate by FTIR, ASTM D5594-18, and 1.8–2.4 g/10 min by ISO 1133-1:2022 under 190°C/2.16 kg. Base compound density is 0.935–0.945 g/cm³, ISO 1183-1:2019, with an unfoamed Shore D hardness of approximately 38, ISO 868:2003. The formulation uses a narrow molecular weight distribution EVA base resin and a stabilizer package that does not contain amine-based antioxidants, which prevents premature consumption of peroxide radicals. In downstream use, the compound is dry-blended with 2–6 phr azodicarbonamide and 0.5–1.2 phr dicumyl peroxide before extrusion or molding. Finished foam density ranges from 0.12 g/cm³ to 0.35 g/cm³, depending on blow ratio, die pressure, accelerator loading, and crosslink density.
Production-scale twin-screw compounding on corotating lines with 44:1 to 52:1 L/D ratios is normally carried out with barrel set temperatures of 90–110°C and screw speeds of 250–400 rpm. At a screw speed of 350 rpm and a set temperature of 110°C, melt temperature measured by an immersed thermocouple typically remains below 125°C, which is below the azodicarbonamide decomposition onset. Field data from continuous foam extrusion lines show that incoming-lot melt flow rate drift outside ±0.10 g/10 min produces measurable changes in cell size distribution. On a 40:1 L/D single-screw foam extrusion line operating at 6 MPa die pressure, the cell size distribution shifts from 0.25–0.40 mm to 0.55–0.70 mm when the melt flow rate increases by 0.15 g/10 min. Die temperature deviation greater than ±5°C from the compound-specific optimum produces surface roughness and elevates open-cell content above 15%. High-shear dispersion of azodicarbonamide agglomerates is required to reach particle sizes below 20 µm; rotor-type batch mixers with intermeshing blades are not recommended for this dispersion threshold.
Compared with common 18 wt% vinyl acetate foamable EVA grades having a melt flow rate of 2.5 g/10 min, the 16 wt% vinyl acetate base compound exhibits lower equilibrium moisture uptake. After 24 h at 23°C and 85% RH, the 160I/21 grade typically absorbs 0.08–0.12 wt% water, whereas 18% vinyl acetate grades can reach 0.18–0.25 wt%, as determined by Karl Fischer coulometry. The lower polar monomer content reduces hydrogen bonding with ambient moisture. Pre-drying at 70–80°C for 2 h in desiccant dryers with a dew point of −40°C is required when ambient relative humidity exceeds 60% or when regrind content is above 20%.
Compared with LDPE-based foamable compounds, the 160I/21 grade provides lower compression set at equal crosslink density and accepts higher filler loadings without complete loss of foam elongation. The continuous service temperature of crosslinked EVA foam is lower than that of crosslinked LDPE foam; EVA-based products are generally limited to 70–80°C, while LDPE foams can operate at 90–100°C. The grade is not silane-grafted; it therefore requires free-radical initiator addition at the conversion stage. This differs from moisture-cure silane foam systems that do not require peroxide addition but demand hot-water or steam exposure for cure completion.
Regrind levels above 20% are permitted only after on-line melt filtration using a 100 µm screen pack and verification of gel fraction. Reusing edge trim from already crosslinked foam is not recommended because crosslinked particles act as nucleating sites and produce microgels of 10–50 µm, observable as surface pinholes after expansion.
In the 160I/21 grade, the recommended crosslinking initiator is dicumyl peroxide, typically applied at 0.5–1.2 phr through a low-temperature tumble blender or gravimetric metering unit. Dicumyl peroxide exhibits a half-life in polyolefin melts of approximately 1 h at 135°C and less than 1 min at 175°C. The practical consequence is that compounding and extrusion zones before the die must remain below 125°C, while the expansion oven or cure section must reach 155–175°C to achieve gel fractions of 62–72%. The initiator decomposes to free radicals that abstract hydrogen from ethylene sequences; the resulting macro-radicals combine to form carbon-carbon crosslinks. At least 60% gel fraction, determined by extraction in boiling xylene per ASTM D2765-16, is required before azodicarbonamide gas evolution reaches its maximum. Lower gel fractions allow cell coalescence and density instability.
Azodicarbonamide decomposition is activated by zinc oxide or zinc stearate. The addition of 0.6–1.0 phr zinc oxide lowers the exothermic decomposition onset from approximately 195°C to 160–170°C. The rate of gas evolution must match the rate of melt strength development. At 3.5 phr azodicarbonamide and 0.8 phr dicumyl peroxide, the gas yield is approximately 220 cm³/g of blowing agent at STP; actual retained gas volume is lower because of diffusion loss through the expanding melt membrane. Foam densities below 0.15 g/cm³ require die pressures above 7 MPa and gel fractions above 65%. Published data for this specific configuration is limited; production validation using in-line rheometry and post-foam density measurement is necessary.
Vinyl acetate content influences vulcanization kinetics because vinyl acetate side groups reduce crystallinity and increase segmental mobility, but also dilute the methylene sequence length available for macro-radical propagation. Compared with a 9 wt% vinyl acetate EVA grade, the 16 wt% vinyl acetate compound typically requires 0.1–0.2 phr higher peroxide addition to reach the same gel fraction at 160°C. This offset should be considered when replacing other EVA grades on existing production schedules.
For compression-molded foam boards, the compound is blended with curative and blowing agent on a two-roll mill at 90–100°C for 8–12 min. The milled preform is then placed into a hydraulic press with platens at 155–165°C and cured under 3–6 MPa for 8–12 min per 10 mm of preform thickness. Venting is initiated during the final 20–30% of cure time when the crosslink density reaches the gel point; premature venting causes blowholes, while late venting produces buckled skins. Mold release agents containing amine functional groups must be avoided because amine functionality can interfere with radical cure and cause surface tack.
The property set below represents typical values obtained from crosslinked foam sheets at 0.20 g/cm³ density after 24 h conditioning at 23°C and 50% RH. Values are not batch release limits unless a specific lot certificate states otherwise.
| Property | Test method | Typical range or value |
| Vinyl acetate content | ASTM D5594-18 | 15.0–17.0 wt% |
| Melt flow rate, 190°C/2.16 kg | ISO 1133-1:2022 | 1.8–2.4 g/10 min |
| Base compound density | ISO 1183-1:2019 | 0.935–0.945 g/cm³ |
| Foam density after expansion | ISO 845:2009 | 0.12–0.35 g/cm³ |
| Tensile strength at 0.20 g/cm³ | ISO 1798:2008 | 2.1–2.8 MPa |
| Elongation at break at 0.20 g/cm³ | ISO 1798:2008 | 180–260% |
| Tear strength | ISO 8067:2018 | 5.5–8.0 kN/m |
| Shore A hardness at 0.20 g/cm³ | ISO 868:2003 / ASTM D2240-15 | 38–48 |
| Compression set 50%, 23°C, 24 h | ISO 815-1:2014 | 25–38% |
| Gel fraction after optimal cure | ASTM D2765-16, xylene extraction | 62–72% |
| Open-cell content, closed-cell foam | ASTM D6226-21 | 0–15% |
Compliance-relevant statements are bounded by the base polymer classification of EVA as an olefinic copolymer under FDA 21 CFR 177.1520 for food-contact use only when the finished foam article is tested for end-use migration. The product is not automatically food-contact compliant in all formulations because azodicarbonamide decomposition residues and peroxide fragments must be assessed. Under EU REACH, the base polymer does not require registration as polymer, but monomer and additive components must be listed or authorized. RoHS 2011/65/EU restrictions apply to lead, cadmium, mercury, hexavalent chromium, PBB, and PBDE in the final converted article; the 160I/21 grade itself is supplied without regulated flame retardants.
The process window is narrower than that of low-melt-index LDPE foam compounds and slightly wider than that of high-vinyl-acetate EVA copolymers above 25 wt% vinyl acetate. Table 2 compares operational parameters at a fixed loading of 3.5 phr azodicarbonamide and 0.8 phr dicumyl peroxide.
| Parameter | EVAtech 160I/21 | 18% VA general-purpose EVA foam grade | LDPE foamable compound | 25% VA EVA foam grade |
| Recommended melt extrusion temperature | 95–110°C | 90–105°C | 110–125°C | 85–100°C |
| Minimum die pressure for closed-cell foam | 6–8 MPa | 5–7 MPa | 7–10 MPa | 4–6 MPa |
| Typical gel fraction at 160°C/8 min | 62–72% | 58–68% | 55–65% | 60–70% |
| Foam density range | 0.12–0.35 g/cm³ | 0.15–0.40 g/cm³ | 0.20–0.45 g/cm³ | 0.10–0.30 g/cm³ |
| Compression set 50%, 23°C, 24 h | 25–38% | 28–42% | 20–30% | 22–35% |
| Continuous service temperature ceiling | 70–80°C | 65–75°C | 90–100°C | 55–65°C |
| Moisture uptake after 24 h at 85% RH | 0.08–0.12 wt% | 0.18–0.25 wt% | <0.05 wt% | 0.30–0.45 wt% |
On the same production line, the 160I/21 grade exhibits less screw slippage than 25% vinyl acetate grades because its lower polarity reduces barrel-wall adsorption in water-cooled feed zones. The main processing penalty compared with LDPE foam is the lower upper temperature limit and the higher pre-drying demand. Compared with 18% vinyl acetate EVA, the grade offers better cell size retention when regrind levels fluctuate between 5% and 20%.
Operational boundaries are explicit: storage in unopened original packaging is recommended at 5–35°C and below 60% RH for 12 months; opened packaging should be consumed within 30 days or re-sealed with desiccant. The product must not be processed in direct contact with copper or copper alloys above 120°C because copper ions can accelerate oxidative decomposition of the peroxide and produce acetyl odor in the foam. Combinations with amine-based nucleating agents, amine-functional silanes, or amine-cured epoxy concentrates are incompatible before the expansion stage. The foam is not inherently UV-stable; outdoor applications require carbon black, titanium dioxide, or hindered amine-free UV stabilizer packages that do not interfere with peroxide cure. When flame retardant grades are required, ammonium polyphosphate or magnesium hydroxide may be incorporated, but the dosage must be compensated by increased peroxide demand. All batches should be verified by torque rheometry and gel fraction analysis before release to full production.