| Código SH | 896504 |
| Conteúdo De Acetato De Vinila | 15% em peso |
| Vazão De Fusão 190 C 2 16kg | 4,0 g /10min |
| Densidade | 0,940 g /cm³ |
| Resistência à Tração Na Ruptura | 24 MPa |
| Alongamento Na Ruptura | 800% |
| Ponto De Fusão | 88 ° C |
| Ponto De Amolecimento Vicat | 62 ° C |
| Shore A Hardness Tradução | 90 |
| Temperatura De Fragilidade | -80 ° C |
| Cristalinidade | Médio |
Como fábrica acreditada HANWHA EVA 1540, aplicamos protocolos de qualidade rigorosos - cada lote é submetido a testes rigorosos para garantir padrões de eficácia e segurança consistentes.
| Embalagem | Disponível em sacos revestidos de polietileno de 25 kg, fornecidos como pellets de resina EVA de fluxo livre para manuseio e armazenamento seguros. |
| Carga de contêiner (20' FCL) | Carga FCL de 20 “de HANWHA EVA 1540: sacos de 25 kg em paletes retráteis, bem arrumados, peso líquido de cerca de 20 toneladas métricas. |
| Envio | HANWHA EVA 1540 é uma resina de copolímero de etileno-acetato de vinila fornecida como pelotas sólidas. Envie como carga não perigosa em sacos selados originais ou contêineres a granel. Mantenha seco, evite luz solar direta e calor alto. Armazene em área bem ventilada, longe de fontes de ignição. Nenhuma classificação especial de transporte necessária. |
| Armazenamento | Armazene HANWHA EVA 1540 em uma área fria, seca e bem ventilada, longe da luz solar direta, calor e chamas abertas. Mantenha os recipientes bem fechados para evitar absorção de umidade e contaminação. Evite o acúmulo de poeira e o contato com oxidantes fortes. Use aterramento adequado contra estática durante o manuseio. Siga as regulamentações locais e mantenha ventilação adequada. |
| Prazo de validade | Armazene fechado em um local fresco e seco, longe da luz solar. A vida útil é de 12 meses a partir da data de fabricação. |
In high-speed carton sealing and PVC edgebanding lines, HANWHA EVA 1540 is processed as a base polymer in gear pump–fed slot-die coaters operating at 160–180°C and line speeds of 60–150 m/min. The grade carries a nominal vinyl acetate content of 15 wt% and a melt index of 4.0 g/10 min when measured under ASTM D1238-20 at 190°C and 2.16 kg; this combination yields a higher cohesive plateau than higher-VA packaging grades while still providing sufficient polar adhesion to coated board, varnish, and PVC edge banding after tackifier addition. A bulk packaging formulation may contain 30–35 wt% EVA 1540, 35–40 wt% C5 aliphatic hydrocarbon tackifier with a ring-and-ball softening point of 95–105°C per ASTM E28-18, 20–30 wt% Fischer-Tropsch wax or refined paraffin wax with a melting point of 65–85°C, and 0.5–1.0 wt% hindered phenolic antioxidant. Brookfield Thermosel viscosity at 180°C under ASTM D3236-15 is generally controlled between 25,000 and 60,000 mPa·s; raising wax content above 30 wt% reduces dynamic shear adhesion on corrugated board with recycled fiber content above 60%, while reducing wax below 18 wt% extends setting time beyond 2.5 s on continuous packaging lines. Thermal stability during production requires closed melt tanks with nitrogen blanketing because the acetate side groups undergo thermolytic elimination of acetic acid at sustained temperatures above 200°C; this degradation mechanism appears on production scales as gradual viscosity drift, char adhesion to gear-pump clearances, and gel speck contamination at the slot-die lip. Bonded assemblies are assessed by T-peel adhesion under ASTM D1876-08 and shear adhesion failure temperature under ASTM D4498-07. For food-contact carton sealing within the European Union, finished hot-melt formulations must comply with Regulation (EC) No 1935/2004 and Regulation (EU) No 10/2011, with an overall migration limit of 10 mg/dm²; in the United States, adhesive components must satisfy FDA 21 CFR 175.105. Edgebanding lines running at 30–50 m/min commonly require partial substitution of petroleum hydrocarbon resin with rosin ester at 20–25 wt% to maintain adhesion to PVC and ABS edge tape, particularly where alcohol-based cleaning agents contact the joint in subsequent assembly steps.
Expansion trials on production compression presses using slab thicknesses of 25–40 mm show that HANWHA EVA 1540 is usually blended with a lower-melt-index EVA containing 18–22 wt% vinyl acetate at a ratio of 70–80 phr EVA 1540 to 20–30 phr of the higher-VA grade to moderate rebound and improve surface skin quality. The foaming system generally comprises azodicarbonamide at 3.0–4.5 phr, dicumyl peroxide at 0.5–0.8 phr, zinc oxide at 1.5–2.5 phr, stearic acid at 0.5–1.0 phr, and calcium carbonate at 5–10 phr as a nucleating filler. Mixing is carried out in an internal mixer or twin-screw compounding extruder with melt temperature held at 85–100°C to avoid premature decomposition of the blowing agent; the compound is then pelletized and compression-molded at 150–160°C under 150–200 kg/cm² for 8–12 min. The critical processing window is defined by competition between dicumyl peroxide crosslinking and azodicarbonamide gas evolution. At dicumyl peroxide loadings above 0.8 phr, crosslink torque onset measured by moving die rheometer under ASTM D5289-17 occurs before the gas yield peak, producing excessive melt strength that traps gas and creates surface fissures; at loadings below 0.45 phr, cell coalescence and internal void formation dominate. Zinc oxide shifts the azodicarbonamide decomposition onset lower by 5–12°C, and when zinc oxide exceeds 3.0 phr, gas evolution can outrun the developing crosslink network and rupture intercellular membranes. Final foam density according to ISO 845 typically falls between 0.16 and 0.22 g/cm³, with Asker C hardness measured under ASTM D2240 in the range of 55–65 for footwear midsole specifications. Compression set tested under ASTM D395-16 Method B at 50% compression, 6 h, and 50°C is usually below 30%. In full-scale production, slabs thicker than 35 mm develop a skin-core density gradient unless the press cooling stage uses a controlled reduction of 0.5°C/min between 120°C and 80°C; rapid cooling by ambient air produces dimensional instability during block splitting. Because HANWHA EVA 1540 contains 15 wt% vinyl acetate, its elastic recovery is lower than that of 22–28 wt% VA grades, so formulations intended for running or high-rebound midsole cells typically blend it with ethylene-octene copolymers at 10–20 phr to raise impact resilience under DIN 53512 while retaining the higher compound melt strength of EVA 1540.
When HANWHA EVA 1540 is selected as the polymer base for low-voltage cable sheathing compliant with IEC 60502-1, the formulation typically loads aluminum trihydroxide at 100–140 phr, magnesium dihydroxide at 20–50 phr, zinc borate at 5–10 phr, a silicone processing aid masterbatch at 3–6 wt%, and a hindered phenolic antioxidant at 0.5–1.0 phr. The 15 wt% vinyl acetate level provides less intrinsic wetting of metal hydrate surfaces than EVA grades with 28 wt% or higher VA; therefore, production-scale twin-screw compounding on corotating extruders with L/D ratios of 40:1–52:1 uses vinyl silane-treated ATH or 2–4 wt% of maleic anhydride-grafted EVA as a coupling interface. Barrel temperatures are maintained at 120–165°C, with ATH introduced through a downstream side feeder at zone 5 or 6 to limit viscosity spikes and to prevent thermal dehydration of ATH, which begins near 180–230°C and releases water vapor that produces porosity and surface roughness on extruded sheath layers. The primary fire-performance indicators for this application are limiting oxygen index under ASTM D2863-19 in the range of 34–38%, halogen acid gas emission under IEC 60754-1 with pH not less than 4.3 and conductivity not exceeding 10 μS/mm, smoke density under IEC 61034-2 with projected light transmittance not less than 60%, and single-wire vertical flame propagation under IEC 60332-1-2. Mechanical acceptance after heat aging is commonly measured by IEC 60811-501 tensile tests, with elongation at break above 160% and tensile strength of 10–14 MPa. A production-scale failure mode occurs when post-consumer recycled EVA or PE waxes with high free acid numbers are added above 5 wt%; acid attack on the metal hydrate filler consumes surface treatment and raises compounding torque beyond the rated gearbox capacity of a 52:1 L/D twin-screw machine. Additionally, barrel zones above 170°C in the devolatilization section increase acetic acid formation from EVA 1540, which can corrode vacuum ports and reduce the effectiveness of zinc borate as a char synergist under cone calorimeter testing to ISO 5660-1.
Carbon black concentrates based on HANWHA EVA 1540 are compounded on corotating twin-screw extruders with screw speeds of 350–500 rpm, barrel temperatures of 130–180°C, and L/D ratios from 36:1 to 48:1. A representative production formulation contains 45–60 wt% EVA 1540, 35–50 wt% furnace carbon black with iodine adsorption number of 80–120 mg/g per ASTM D1510-21, 3–5 wt% polyethylene wax, and 0.3–0.5 wt% hindered phenol antioxidant. The 4.0 g/10 min melt index of EVA 1540 is low enough to retain strand geometry after underwater pelletizing at water temperatures of 20–35°C, but high filler loading increases melt viscosity to the point that gear-pump inlet pressure must be monitored below 80 bar to prevent screw thrust bearing overload. Screw configuration uses high-shear kneading elements upstream of carbon black feed to break down pelletized feedstock, then low-shear conveying sections after the side feeder to limit carbon black attrition and acetate ester degradation. Filter packs with 100/200/100 mesh screens are placed ahead of the die plate; a pressure rise above 30 bar triggers screen pack change and is used as an empirical agglomerate warning. The masterbatch is let down at 2–4 wt% in linear low-density polyethylene film to obtain a carbon black concentration of 2.5–3.0 wt%, at which point UV weathering resistance of agricultural film is evaluated under ISO 4892-3 and tensile retention after exposure under ISO 527-3. Pellet attrition during pneumatic conveying is minimized by maintaining pellet water quench temperature between 20°C and 35°C and by adding 0.5–1.0 wt% ethylene bis-stearamide as a surface lubricant; higher levels above 1.5 wt% reduce strand cooling efficiency and cause brittle pellet fracture at the pelletizer rotor. Because the vinyl acetate content of EVA 1540 contributes to a lower melt point than high-density polyethylene carriers, converter-side screw dosing in the feed throat must be set below 40°C throat temperature to avoid premature softening and bridging on single-screw film extruders.
On torch-on bituminous waterproofing membrane lines, HANWHA EVA 1540 is compounded at 6–10 wt% in oxidized bitumen feedstock using high-shear rotor-stator mixers at 175–185°C for 2–3 h before calendering onto nonwoven polyester or glass-fiber carriers. The blend typically includes mineral filler at 20–30 wt% and may include atactic polypropylene at 5–10 wt% when lower melt viscosity at torch-on temperature is required. Softening point is measured under ASTM D36-14, penetration at 25°C under ASTM D5-20, low-temperature flexibility under ASTM D146-17, and tensile properties under ASTM D638-14 after conditioning at 23±2°C and 50±5% relative humidity. The addition of EVA 1540 raises the softening point of a 70/100 pen bitumen from approximately 45°C to 85–105°C depending on filler loading and shearing history. Published data specific to EVA 1540 in this exact formulation window is limited; screening under EN 13707 flexural cold bending and EN 12730 static indentation methods is required before roofing technical approval. A production-scale constraint is that prolonged mixing above 190°C increases acetic acid generation from the vinyl acetate groups, which accelerates oxidation of the bitumen phase and reduces low-temperature flexibility measured by ASTM D146. This application is limited to torch-applied waterproofing systems and should not be extended to emulsified asphalt cold-applied coatings without separate compatibility testing because the EVA phase destabilizes cationic emulsions containing fatty amine emulsifiers.
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