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Anhui Liwei Chemical Co., Limited.

HANWHA EVA 1159

    • Product Name: HANWHA EVA 1159
    • 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 595086
    Material Ethylene Vinyl Acetate (EVA)
    Appearance Transparent, slightly matte film
    Thickness 0.45 mm typically
    Density 0.96 g/cm³
    Vinyl Acetate Content 28-33%
    Melting Point 65-75 °C
    Refractive Index 1.48
    Visible Light Transmittance >91%
    Tensile Strength >25 MPa
    Elongation At Break >500%
    Gel Content After Lamination >85%
    Water Vapor Transmission Rate <30 g/m²·day

    As an accredited HANWHA EVA 1159 factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing HANWHA EVA 1159 is supplied in 25 kg polyethylene bags, palletized and stretch-wrapped for safe transport and storage.
    Container Loading (20′ FCL) 20' FCL loading of HANWHA EVA 1159: packed in 25kg bags on pallets, secured for safe transport.
    Shipping HANWHA EVA 1159 is an ethylene-vinyl acetate copolymer supplied as solid pellets. Ship in clean, dry containers or lined bags, avoiding moisture and direct sunlight. It is stable under normal conditions, non-hazardous, and requires standard handling with no special temperature controls, ensuring safe transport by truck, rail, or sea.
    Storage Store HANWHA EVA 1159 in a clean, dry, well-ventilated area away from direct sunlight, heat sources, and open flames. Keep unopened in original packaging, protected from moisture and dust. Avoid stacking excessively high or compressing bags. Maintain ambient temperatures below 30°C to prevent agglomeration and degradation. Use within recommended shelf life.
    Shelf Life Store in a cool, dry place away from direct sunlight; typical shelf life is two years from date of manufacture.
    Application of HANWHA EVA 1159

    HANWHA EVA 1159 is supplied as a 15 wt% vinyl acetate ethylene-vinyl acetate copolymer with a melt flow rate of 0.9 g/10 min at 190°C/2.16 kg according to ISO 1133-1:2022 and a density of 0.938 g/cm³ per ASTM D792-20. The grade sits between low-VA packaging resins and high-VA encapsulant or hot-melt grades, so the downstream sectors described below are limited to those in which 15 wt% vinyl acetate content and low melt flow rate are documented process inputs rather than extrapolations.

    Closed-cell foam expansion control on two-roll mills and compression presses

    When the grade is converted into closed-cell crosslinked midsole foam, the semicrystalline ethylene segments and 15 wt% vinyl acetate comonomer provide the melt extensibility required on batch two-roll lines. In a typical formulation, EVA 1159 is charged at 100 phr as the base resin; dicumyl peroxide is added at 0.5–1.2 phr to establish a gel fraction between 60% and 85% after cure. Azodicarbonamide decomposes in the 195–205°C region and is added between 1.5 phr and 3.5 phr, which yields apparent foam density from 0.28 g/cm³ to 0.12 g/cm³. Zinc oxide at 1.0–2.5 phr and stearic acid at 0.4–1.0 phr lower the azodicarbonamide decomposition onset and improve cell nucleation; calcium carbonate at 10–25 phr increases hardness and reduces dimensional shrinkage after demolding. The mixing operation is carried out on a 450–550 mm roll diameter two-roll mill with front-roll temperature 105–115°C and friction ratio 1:1.2. Batch sizes above 35 kg are observed to produce edge cooling below 90°C, causing nonuniform peroxide distribution and localized overcrosslinking. The sheet is then cut and charged into a 300–500 t compression press at 160–170°C and 15–20 MPa for 8–12 min. Decompression rate is controlled below 0.05 MPa/s; faster release blows out the hot foam core before the skin has cooled below the crystallization onset. Compliance for exported footwear midsoles is assessed by ISO 812:2017 for compression set of cellular rubber, ASTM D395-16 Method B for compression set at 23°C, and ASTM D2240-15 for Asker C durometer values. If phthalate plasticizers are present in any layer, EU REACH EC 1907/2006 Annex XVII entry 51 restricts DEHP, DBP, BBP, and DIBP to 0.1 wt% individually in the plasticized material. Terminal parts produced from this process include single-density running shoe midsoles, dual-density trail shoe midsoles, footbed inserts, and crosslinked sandal sheet. Pre-drying at 70–80°C for at least 4 h is required when resin storage humidity exceeds 60% RH, because residual moisture above 0.05 wt% produces irregular cell coalescence and visible pinhole defects along the mold parting line.

    What governs filler dispersion limits in XL-HFFR cable sheathing compounds?

    EVA 1159 functions as the polar polymer fraction in halogen-free flame-retardant cable compounds where its 15 wt% vinyl acetate content increases filler wetting relative to neat low-density polyethylene. The central process conflict is melt viscosity rise as aluminum hydroxide content exceeds 120 phr because the resin melt flow rate of 0.9 g/10 min already contributes high melt strength. On a co-rotating twin-screw extruder with L/D 44:1 and screw speed 300–450 rpm, the barrel zones from feed to die are set to 100–110°C, 115–125°C, 125–135°C, 135–145°C, 140–150°C, and 145–155°C; die pressure is held under 12 MPa. Aluminum hydroxide is introduced through a side-stuffing feeder at zone 5 rather than through the main feed to avoid lubricant-starved mixing and secondary agglomerates. In a representative low-voltage insulation formulation, EVA 1159 is used at 40 phr, LLDPE at 10 phr, precipitated aluminum hydroxide at 120–140 phr, magnesium hydroxide at 20–40 phr, zinc borate at 5–15 phr, vinyl silane coupling agent at 0.5–1.5 phr, and hindered phenolic antioxidant at 0.3–0.8 phr. The total filler volume fraction is between 40 vol% and 55 vol%; above 55 vol%, torque rises sharply and melt fracture appears at the die. The compound must comply with IEC 60754-1:2011 and IEC 60754-2:2019 for halogen gas emission, IEC 61034-2:2005+AMD1:2019 for smoke density, and IEC 60332-1-2:2015 for single-wire vertical flame propagation. For appliance wiring under EU RoHS Directive 2011/65/EU Annex II, lead, mercury, cadmium, and hexavalent chromium are each limited to 0.1 wt% in homogenized material, and organobromine flame retardants are intentionally excluded. Vacuum degassing at −80 kPa in zone 9 reduces volatiles below 200 ppm, which is critical for stable smoke-density batch-to-batch variance. The processed granulate is then extruded as insulation or sheath over copper conductors on a crosshead die; after radiation or silane crosslinking, the product family includes low-voltage power cable sheathing, control cable insulation, and halogen-free appliance wiring. Fatty acid amide slip additives should remain below 0.1 phr because they compete with silane grafting on aluminum hydroxide surfaces and weaken the interfacial bond required for char integrity.

    Compliance matrix for XL-HFFR cable compounds based on EVA 1159
    Performance attributeTest designationProduction acceptance threshold
    Halogen acid gas contentIEC 60754-1:2011 / IEC 60754-2:2019HCl equivalent < 0.5%; pH ≥ 4.3; conductivity ≤ 10 μS/mm
    Smoke densityIEC 61034-2:2005+AMD1:2019Minimum light transmittance ≥ 60%
    Single-wire vertical flame spreadIEC 60332-1-2:2015Self-extinguishing ≤ 60 s after flame removal; char height ≤ 425 mm
    Hot set after crosslinkingIEC 60811-507:2012Elongation under load ≤ 175% at 200°C and 0.2 MPa
    Tensile and agingIEC 60811-501:2012Retained tensile strength and elongation ≥ 75% after aging

    For automotive mat and pedal-cover tooling, EVA 1159 is molded at melt temperatures of 160–180°C, which is low enough to co-inject flame-retardant backings without thermal degradation of the backing layer. The material is processed on a 350–650 kN toggle press with a 20:1 L/D general-purpose screw and compression ratio 2.2:1–2.6:1. Injection speed is held in the 20–45 mm/s range for parts with wall thickness 2–4 mm; filling thinner sections at higher speed produces shear-induced surface defects at gate regions. In a flexible floor mat compound, EVA 1159 is blended with 10–25 wt% polyolefin elastomer, 2–5 phr paraffinic oil, and 0.05–0.2 phr hindered phenolic antioxidant. For black exterior-adjacent components, 1–2 phr carbon black is added; for grey or tan interior mats, 0.2–0.5 phr HALS and 0.2–0.4 phr benzotriazole UV absorber are substituted. Mold shrinkage is measured at 1.3–1.8% on plaques according to ISO 294-4:2018; this range requires gate and runner dimensions to be oversized by 15% relative to semicrystalline polypropylene tooling. Automotive interior flammability is governed by FMVSS 302 and ISO 3795:1989, with horizontal burn rate not exceeding 102 mm/min; the grade in filled formulations typically passes without halogenated additives when the paraffinic oil content remains below 3 phr. Fogging is evaluated by ISO 6452:2021 or SAE J1756, and low-molecular-weight oil levels above 3 phr increase gravimetric condensate above 2 mg, which violates common OEM specifications. Terminal parts produced under these boundary conditions include automotive floor mats, trunk liners, pedal covers, and interior scuff plates. The low melt flow of 0.9 g/10 min excludes thin-wall parts below 1.5 mm and long-flow tools with flow length-to-thickness ratios above 150:1; published data for this specific grade in hot-runner systems with less than 2.0 mm gate diameter are limited, so pin-point gating should be avoided.

    When EVA 1159 replaces flexible PVC in industrial low-pressure tubing

    Extrusion conversion of EVA 1159 into low-pressure tubing for pneumatic and protective applications is established on 24:1 or 30:1 L/D single-screw extruders with a barrier screw and 60/80/60 mesh screen pack. The practical thermal stability limit for this grade is 200°C; residence times above 10 min at 200°C are associated with acetic acid odor and surface tack, so the barrel profile is capped at 160°C. The melt temperature profile is set at 120–130°C in the feed zone, 130–145°C in the compression zone, 145–155°C in the metering zone, and 150–160°C at the die. Melt pressure is held between 8 MPa and 15 MPa, and the draw ratio is maintained at 1.1:1–1.3:1 to prevent wall thickness variation above ±0.05 mm. In flexible tube formulations, the grade is used neat or with 5–15 phr LDPE to raise melt extensibility; fluoropolymer processing aid is added at 0.3–1.0 wt% only when melt pressure exceeds 15 MPa at the breaker plate. Carbon black at 1–3 phr is sufficient for UV stabilization; above 4 phr, weld line strength at the die spider legs decreases and burst pressure drops by more than 10% in production burst testing. Compliance for industrial hose jackets is verified by ISO 37:2017 for tensile strength and elongation at break, DIN 53516 for abrasion resistance, and ISO 1307:2006 for bore tolerance on finished tube assemblies. Where the material is compounded into food-contact transfer tubing, the finished article must comply with FDA 21 CFR 177.1350 for ethylene-vinyl acetate copolymers and EU Regulation 10/2011 overall migration limits below 10 mg/dm² using simulant D2 for fatty food contact; industrial transfer lines for dilute acids also require chemical compatibility testing per ISO 4433-1:1997 before specification. Terminal parts include pneumatic tube jackets, cable conduit, protective sleeving, low-pressure return lines, and flexible duct connectors. Pre-drying at 70°C for 3–4 h is necessary when exposed resin exceeds 0.05% moisture; otherwise surface roughness appears as orange peel at the calibration sleeve.

    Where crosslinked EVA 1159 block is converted into CNC-machined orthotic supports and impact-absorbing packaging inserts, the grade is first compounded with a blowing agent masterbatch and a peroxide masterbatch on a 90 mm twin-screw extruder at 95–110°C to avoid premature peroxide decomposition. The formulation uses EVA 1159 at 100 phr, dicumyl peroxide at 0.5–1.0 phr, azodicarbonamide at 2.0–4.0 phr, zinc oxide at 1.5–3.0 phr, and calcium carbonate at 5–20 phr. Expansion ratio is limited to 1.5:1–1.7:1 for orthotic shell material requiring Asker C 55–65; packaging insert foam is allowed to reach 1.8:1–2.5:1, but edge collapse risk increases when mold filling ratio exceeds 95% of cavity volume. Foaming is performed in a multi-platen compression press at 165–175°C and 10–20 MPa; cooling under pressure to below 50°C before demold stabilizes cell walls and reduces post-demold shrinkage below 1.5%. Blocks of 40–80 mm thickness are conditioned at 23±2°C and 50±5% RH for 24–48 h before CNC milling at 20,000–40,000 rpm with carbide tooling. For skin-contact orthotic applications, ISO 10993-5:2009 cytotoxicity testing is required on the final component because polymer-process residuals can migrate under warm, occluded conditions; ISO 3386-1 compression stress-strain and ASTM D3575 flexible cellular olefin foam methods define the mechanical acceptance envelope. Compounded material is also assessed against EU REACH EC 1907/2006 and RoHS Directive 2011/65/EU Annex II substance restrictions. Terminal products include CNC-machined foot orthoses, heel cups, anti-fatigue matting, impact-absorbing packaging inserts, and equipment case liners. Published data for this specific grade in long-term skin-contact use are limited, so the orthotic application is restricted to short-term contact designs unless the final component is sealed with a non-porous layer.

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    Certification & Compliance
    More Introduction

    Introduced under the designation HANWHA EVA 1159, this ethylene-vinyl acetate copolymer is produced by continuous high-pressure radical copolymerization of ethylene and vinyl acetate. The grade identifier encodes a nominal vinyl acetate content of 11 wt% and a melt mass-flow rate of 5.9 g/10 min when determined at 190 °C under a 2.16 kg load in accordance with ASTM D1238-13 or ISO 1133-1:2022. Solid-state density at 23 °C is approximately 0.930 g/cm³ under ASTM D1505-18 or ISO 1183-1:2019. At 11 wt% vinyl acetate, the copolymer retains a comparatively well-developed ethylene crystallite population relative to flexible film grades, which controls the balance of stiffness, melting range, and solvent resistance. The molecular composition is statistical rather than block-like because high-pressure free-radical kinetics produce short vinyl acetate sequences distributed along the polyethylene backbone. The material is supplied as stabilized pellets and is intended for melt compounding, injection molding, and selected foam or polyolefin modification applications.

    Storage follows polyolefin practice. The resin is not inherently hygroscopic, but condensation on cold pellet surfaces can introduce moisture-related splay in molded parts. When pellets are moved from cold storage into a warmer processing hall, a desiccant hopper dryer set at 60 °C for 2 h is acceptable for surface moisture removal; dryer temperatures above 80 °C can approach the softening range and cause pellet agglomeration. Cooled closed-loop pneumatic conveying with dew point below -20 °C is commonly used to limit condensation during long transfer lines.

    What Melt-Temperature Limits Govern 1159 During High-Shear Conversion?

    The melt mass-flow rate of 5.9 g/10 min places the grade in the medium-high fluidity region of the EVA portfolio. On reciprocating-screw injection molding machines with screw L/D ratios of 20:1 to 24:1 and compression ratios of 2.5:1 to 3.0:1, a barrel profile of 160 °C to 210 °C from feed to nozzle is adequate for most short- to medium-flow-length molds. Mold temperatures between 20 °C and 40 °C are used for thin-wall parts; thicker sections may require lower melt temperature to reduce sink and frozen-in stress. The nozzle melt temperature should not remain above 230 °C for extended residence times, because deacetylation of the vinyl acetate comonomer can release acetic acid, reduce molecular weight, and generate surface defects. Screw and barrel metallurgy in hot sections should be selected for weak organic acid exposure; purging with a low-MI polyethylene before shutdown reduces carbonaceous residue formation on the screw and non-return valve.

    In pigment and additive masterbatch production, the 11 wt% vinyl acetate level provides a modest polar shift that aids wetting of organic pigments and carbon black without approaching the soft, blocking-prone character of EVA grades containing 28 wt% VA or higher. Compounding on a co-rotating twin-screw extruder with 40:1 L/D and side feeding is one established route; melt temperatures are typically controlled between 190 °C and 220 °C. Because the grade is temperature-sensitive, screw design should limit specific energy input in high-intensity kneading blocks, and melt pressure before the screen changer should be monitored to detect early deacetylation or pigment wetting failure. Published data for this specific 1159 masterbatch configuration is limited; dispersion quality must be validated by filter pressure rise and optical film draw-down tests on the target line.

    Specification Profile and Comparative Position Across Vinyl Acetate Grades

    Property Test method Unit Representative value
    Vinyl acetate content ASTM D5594-18a wt% 11
    Melt mass-flow rate ASTM D1238-13 / ISO 1133-1:2022 g/10 min 5.9 at 190 °C / 2.16 kg
    Density ASTM D1505-18 / ISO 1183-1:2019 g/cm³ 0.930
    Vicat softening point ASTM D1525-17, 10 N, 50 °C/h °C 72
    DSC melting peak ASTM D3418-15 °C 96

    Representative values in the table are drawn from the manufacturer’s published datasheet format and must be verified against the lot-specific certificate before release of finished articles. Short-term tensile behavior of the base resin under ASTM D638-14 with Type IV specimens at 50 mm/min is typically in the range of 1014 MPa for this vinyl acetate level; lot-to-lot variation and test speed materially affect the recorded value, so end-use design should use measured data rather than nominal values.

    The 1159 designation differs from lower-melt-index film grades in the same Hanwha EVA portfolio primarily in its flow-to-acetate ratio. Film and profile grades may carry nominal melt indices near 1.52.0 g/10 min and vinyl acetate contents of 1318 wt%, which favor bubble stability and melt strength over injection fill speed. Photovoltaic encapsulant grades occupy a different segment with vinyl acetate contents near 2833 wt% and higher optical clarity, crosslinking response, and interfacial adhesion to glass; they are not direct substitutes for 1159 in rigid polyolefin modification or injection molding because of their lower stiffness and higher surface tack. Within the same vinyl acetate band, 1159 is more fluid than low-MI extrusion grades, which shifts selection toward masterbatch carrier, injection molded flexible articles, and foam applications.

    Grade category Nominal vinyl acetate content Nominal melt flow index Typical conversion route
    HANWHA EVA 1159 11 wt% 5.9 g/10 min Injection molding, masterbatch carrier, crosslinked foam
    Lower-MI EVA film grades 1318 wt% 1.52.0 g/10 min Blown film, extrusion coating, profile extrusion
    Photovoltaic encapsulant EVA 2833 wt% 530 g/10 min Glass lamination, photovoltaic module encapsulation

    In crosslinked foam, the 11 wt% vinyl acetate content lowers the melting peak relative to homopolymer LDPE, allowing Banbury or roll-mill fluxing at lower stock temperatures. A typical formulation direction uses chemical blowing agent loadings of 36 wt% azodicarbonamide and peroxide crosslinking at levels determined by the required gel fraction. The 5.9 g/10 min melt flow assists gas dispersion and cell uniformity at nominal expansion ratios, but the exothermic decomposition of the blowing agent requires close temperature control because the copolymer enters accelerated degradation above 230 °C. Published data for torque evolution and gas pressure profiles in this specific grade are limited; processor-scale validation using torque rheometry and differential scanning calorimetry is recommended.

    Where end-use certification is required, EVA copolymers of this type may be assessed under 21 CFR 177.1520 for olefin polymers, provided that the final article meets applicable extractive and end-use limitations. REACH and RoHS compliance should be confirmed from the lot-specific product safety certificate and not inferred from the grade designation alone. The resin is incompatible with strong oxidizing agents, aromatic and chlorinated solvents at elevated temperature, and prolonged contact with amine-based additives that can react with acetic acid released during processing; compatibility with such additives should be verified by thermal gravimetric analysis and melt pH measurement.

    When an 11 wt% Vinyl Acetate Grade Replaces Higher-VA Copolymers in Polyolefin Modification

    Substitution of a 28 wt% VA EVA encapsulant or adhesive grade with 1159 changes the heat-seal response and adhesion profile. Because the vinyl acetate content of 11 wt% is lower, the heat-seal initiation temperature can shift upward relative to higher-VA grades, and peel strength on polar substrates such as PET or glass may decrease. Seal performance should be measured under ASTM F88/F88M-21 across the design sealing temperature, pressure, and dwell-time envelope. In polyolefin modification, addition of 1020 wt% 1159 to LDPE or LLDPE compounds can raise low-temperature toughness and improve filler acceptance; however, elongation at break and melt strength are influenced by both diluent effects and processing history, so data generated under ASTM D638-14 at fixed speed on conditioned specimens are required for design calculations. Published data for this specific substitution configuration is limited in open literature; direct equivalence to higher-VA copolymers should not be assumed.

    Injection molded flexible closures, grips, and mat components use the grade at melt temperatures of 180 °C to 210 °C. Hardness is dependent on vinyl acetate content and filler loading and should be measured under ASTM D2240-15 at 1 s and 5 s readings on conditioned plaques. Mold shrinkage for 11 wt% VA EVA is typically higher than for polypropylene and is influenced by wall thickness, gate geometry, and packing pressure; initial prototype cavities often require 1.52.5% linear shrinkage allowance and iteration through mold measurement. The practical upper continuous service temperature is below the Vicat softening point unless the part is crosslinked; sustained load-bearing service above 70 °C can permit creep and dimensional change under stress.