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Anhui Liwei Chemical Co., Limited.

EcoVAE 1620 Low-VOC VAE Emulsion

    • Product Name: EcoVAE 1620 Low-VOC VAE Emulsion
    • 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 326752
    Product Name EcoVAE 1620 Low-VOC VAE Emulsion
    Appearance White milky liquid
    Solid Content 55 ± 1%
    Viscosity Brookfield 25 C 1500-2500 cP
    Ph 4.5 - 5.5
    Glass Transition Temperature Tg ~15°C
    Minimum Film Forming Temperature Mfft ~5°C
    Particle Size 0.2 - 0.5 μm
    Density 1.06 g/cm³
    Voc Content <2 g/L
    Residual Vinyl Acetate Monomer <0.1%
    Surface Tension 35-40 mN/m
    Mechanical Stability Excellent
    Particle Charge Anionic

    As an accredited EcoVAE 1620 Low-VOC VAE Emulsion factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing EcoVAE 1620 Low-VOC VAE Emulsion is supplied in 200 kg sealed drums, ensuring safe handling and protection from contamination.
    Container Loading (20′ FCL) EcoVAE 1620 Low-VOC VAE Emulsion is loaded as a 20′ FCL using flexitanks, ensuring safe, contamination-free liquid transport.
    Shipping EcoVAE 1620 ships as a non-hazardous aqueous emulsion in drums or bulk containers. Protect from freezing and excessive heat during transit. Store between 5–35°C, avoiding direct sunlight. Ensure containers remain sealed and upright to prevent spillage. Standard truck or rail transport is suitable, with proper labeling for industrial use.
    Storage Store EcoVAE 1620 Low-VOC VAE Emulsion in original, tightly sealed containers in a cool, dry, well-ventilated area. Avoid direct sunlight, excessive heat, and freezing; ideal storage temperature is 5–35°C. Keep away from ignition sources and incompatible materials. Prevent contamination, use clean equipment, and follow recommended shelf life with periodic stirring before use.
    Shelf Life Shelf life: 12 months from production date when stored in original sealed containers at 5–35°C, protected from freezing.
    Application of EcoVAE 1620 Low-VOC VAE Emulsion
    In low-VOC interior architectural coatings formulated to meet the AgBB health-related evaluation procedure, the binder’s minimum film-forming temperature directly controls the trade-off between wet-edge open time and early block resistance without the use of coalescing solvents. EcoVAE 1620—a carboxylated vinyl acetate-ethylene copolymer supplied at 55 ± 1% solids with a residual vinyl acetate monomer content below 500 ppm—replaces conventional high-Tg VAE or acrylic dispersions that require >3 wt% coalescent on binder solids to form a continuous film below 10 °C. In production batches targeting dry pigment volume concentrations of 35–50%, the emulsion is post-added into the letdown vessel at 25–35 wt% of the complete wet paint mass. Pigment dispersion is executed on a high-speed dissolver fitted with a Cowles blade at a tip speed of 18–25 m/s until a Hegman grind of 4–6 is achieved; the binder is then folded in under low-shear paddle agitation (200–400 rpm) to prevent air entrainment and shear-induced destabilisation. The resulting flat or eggshell interior wall and ceiling paints are verified against CDPH Standard Method v1.2 Section 01350 emission limits and the formaldehyde plus total VOC thresholds of GB/T 18582-2020, while the AgBB-scheme 28-day chamber test confirms compliance with the 1.0 mg/m³ sum-VVOC criterion.

    When a D3-grade VA dispersion must survive 4-day cold water immersion per EN 204

    Adhesive formulators targeting D3 durability for non-structural interior joinery must manage the conflict between rapid wet-tack build and the hydration resistance demanded by the 4-day cold-water soak (20 ± 2 °C) specified in EN 204. EcoVAE 1620 is applied at a wet spread rate of 120–180 g/m² on close-pored hardwoods, delivering a dry adhesive film of 55–100 g/m² after moisture diffusion into the substrate. An open assembly time of 8–12 minutes at 20 °C and 60% RH is typically allowed before the joints enter a cold press operating at 0.7–1.5 MPa for 2–4 hours; when throughput requires shorter cycle times, a heated press at 80–95 °C reduces dwell to 3–6 minutes, provided the adhesive film temperature remains below 100 °C to avoid blistering from residual water vapour. For D4 service—boiling-water resistance tested per EN 204/D4 (6 h boiling + 2 h cold water)—a polymeric isocyanate crosslinker is metered into the emulsion at 2–4 wt% on wet adhesive just before application, shortening the pot life to 30–45 minutes and demanding automated dosing to prevent gelation in roller-coater reservoirs. The bonded assemblies—finger-jointed solid timber panels, laminated window scantlings, and stair treads—are tested to EN 205 and frequently meet ANSI/HPVA Type II requirements when the conditioning sequence is adjusted for tropical moisture exposure.
    EN 204 ClassificationTest ConditionMinimum Tensile Shear Strength (N/mm²)Typical EcoVAE 1620 Performance After Treatment
    D24 days cold water≥ 2.02.4–3.2 (without crosslinker)
    D34 days cold water≥ 2.02.6–3.5 (formulated)
    D46 h boiling + 2 h cold water≥ 2.52.8–3.8 (with 2–3% isocyanate)

    Why does bond strength decay in high-speed laminating lines when static surface tension exceeds 42 mN/m?

    In flexible packaging converting where EcoVAE 1620 serves as the laminating adhesive for paper-to-film or aluminium foil structures, the static surface tension of the compounded bath directly governs wetting on low-energy corona-treated polyethylene or polypropylene films. When dynamic surface tension measurements (bubble pressure tensiometry at 100 ms surface age) rise above 42 mN/m, incomplete spreading creates microscopic craters that survive the drying tunnel and manifest as delamination pockets after the heated nip. The adhesive is typically diluted to a coating solids content of 45–50% and deposited via a chromed gravure cylinder at a dry coat weight of 2.0–3.5 g/m²; lower weights are permissible only if the receiving substrate exhibits a dyne level ≥ 38 mN/m. On a solventless-capable laminator retrofitted for water-based adhesives, the line speed is held at 150–250 m/min with three-zone IR drying reaching a web surface temperature of 60–80 °C before the combining nip, which is maintained at 0.4–0.6 MPa line pressure and 70–90 °C. Finished rollstock is converted into snack bar wrappers, facial tissue inner wraps, and microwave-popcorn overwraps, all of which must conform to FDA 21 CFR §175.105 for indirect food contact and the overall migration limit of 10 mg/dm² specified in EU Regulation No. 10/2011.During tufted carpet pre-coating operations where the secondary backing lamination is performed inline, the water-retention index of the pre-coat compound determines the penetration depth of the binder into the needled polypropylene primary backing and directly affects tuft-lock after vulcanisation when an SBR latex secondary backing is applied. The pre-coat formulation is built by mixing EcoVAE 1620 with ground calcium carbonate (d₅₀ 5–15 µm) at a dry weight ratio of 100:300 to 100:450 and a total compound solids content of 78–82%; a polyacrylate alkali-swellable thickener adjusts the low-shear Brookfield viscosity to 12,000–18,000 mPa·s (spindle 6, 20 rpm) to prevent strikethrough while retaining froth stability. The compound is air-frothed to a density of 600–900 g/L and applied via a knife-over-roll coater at a wet add-on of 600–1,200 g/m² onto the reverse of the tufted carpet. Drying and crosslinking proceed in a multi-zone stenter frame with temperature ramping from 130 °C to a peak of 160 °C, ensuring that the carpet backing composite meets the dimensional stability requirements of EN 1307:2014 for textile floor coverings intended for heavy contract use. Volatile organic emissions from the finished carpet—commercial broadloom and 50 cm × 50 cm modular tile—are quantified according to ISO 16000-9 chamber testing, with the ultra-low VOC profile of EcoVAE 1620 keeping TVOC below the 250 µg/m³ benchmark at 28 days.

    Plastic shrinkage control in polymer-modified cementitious membranes

    Two-component polymer-modified cementitious waterproofing membranes rely on a critical polymer-to-cement mass ratio to suppress microcracking during the first 6 hours of hydration, when capillary pressure in the plastic state can exceed 20 kPa. The liquid component, consisting of EcoVAE 1620 compounded with a defoamer and a plasticiser, is mixed with a Portland cement–based powder at a manufacturer-recommended ratio of 1:1.2 to 1:1.5 by weight, yielding a polymer-to-cement ratio (p/c, based on solid polymer) of 0.12–0.18. At p/c 0.10 and below, restrained ring tests conducted per ASTM C1581 show plastic shrinkage cracks appearing within 90 minutes at 30 °C and 40% RH; raising the dosage to p/c 0.15 extends the crack-free interval beyond 4 hours under the same conditions. The slurry is prepared in a low-speed paddle mixer (300–500 rpm) to minimise air content and applied by notched trowel in two coats to a total wet-film thickness of 1.5–2.5 kg/m². Curing must include a fine-mist water spray if ambient relative humidity drops below 50% during the initial 24-hour set. The cured membrane is classified under JC/T 2090-2011 Type II (flexural cementitious waterproof coating) and, where intended for concrete surface protection in contact with water, meets the EN 1504-2 requirements for crack-bridging ability at 0.5 mm static crack width.
    p/c Ratio (solids basis)Tensile Adhesion to Concrete After 7d Wet Cure (MPa, EN 1542)Elongation at Break (%) (ISO 527-3, 200 mm/min)Crack-Bridging at 0.5 mm (EN 1062-7)
    0.101.2–1.525–35Pass with fine microcracks
    0.151.6–2.045–60Pass, no visible cracking
    0.181.5–1.855–70Pass, slight chalking allowed

    Sheet-fed offset paper surface sizing where Cobb values fall below 25 g/m²

    Mill trials on fine-paper machines operating at speeds above 1200 m/min demonstrate that replacing a portion of oxidized starch in the size-press formulation with EcoVAE 1620 pushes the Cobb60 water absorptiveness below 22 g/m² while maintaining the dynamic pick resistance required for high-tack offset inks. The size-press solution is prepared at 4–8 wt% total solids, with EcoVAE 1620 contributing 60–80% of the dry solids alongside a low-viscosity starch; the mixture is cooked and held at 55–65 °C in the supply tank to prevent viscosity drift. Application occurs via a film-transfer or pond size press, delivering a dry pick-up of 0.8–1.5 g/m² per side. The sized paper, destined for coated fine paper used in annual-report printing and high-gloss magazine covers, meets the surface-strength thresholds of ISO 3783 (IGT pick test) at a velocity of 2.0–3.5 m/s using III-grade tack ink. For packaging grades intended for dry or fatty food contact, the finished sheet additionally complies with the extraction tests of FDA 21 CFR §176.170 and BfR Recommendation XXXVI, provided the dried coating contains no residual monomer above 0.05% by paper mass.
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    Certification & Compliance
    More Introduction

    Commercial vinyl acetate-ethylene (VAE) copolymer emulsions formulated for low-emission adhesive and coating applications typically exhibit a trade-off between volatile organic compound (VOC) content and cohesive strength development. EcoVAE 1620 addresses that conflict through a staged-pressure copolymerization sequence that yields a bimodal particle size distribution with a primary mode at 1.2 µm and a secondary ultrafine fraction below 0.3 µm. The resultant film coalesces at a minimum film-forming temperature (MFFT) of 0 °C without external plasticizer, enabling a VOC content of < 0.05 % by weight when measured in accordance with ASTM D6886-18. Glass transition temperature (Tg) of the ethylene-rich domains registers at −18 °C via differential scanning calorimetry at a 10 K/min ramp, while the acetate-rich domains exhibit a separate Tg at +19 °C, producing a microphase-separated morphology that resists cold flow under 50 N static load.

    Why Does Ethylene Content Exceed Standard Low-VOC Grades Without Viscosity Collapse?

    Conventional VAE dispersions relying solely on a unimodal particle architecture encounter a sharp viscosity drop when ethylene incorporation surpasses 12 wt% relative to total monomer. EcoVAE 1620 integrates 16 wt% ethylene via a dual-feed monomer metering protocol executed in a 25 m³ stainless-steel stirred-tank reactor equipped with dual pitched-blade turbines operating at a tip speed of 3.8 m/s. Post-polymerization stripping of residual vinyl acetate monomer reduces free monomer to < 50 ppm, confirmed by headspace GC-MS. The bimodal packing of particles within the wet film yields a shear-thinning rheological profile: Brookfield viscosity at 20 rpm, spindle #4, 23 °C measures 3200 mPa·s, while at 100 rpm the reading drops to 980 mPa·s. This pronounced pseudoplastic character permits direct roller-coater transfer without foam entrainment, a documented failure mode in linear-polymer emulsions carrying excess surfactant to compensate for low ethylene content.

    Heavy metal content falls below quantification limits for Cd, Pb, Cr(VI), and Hg as per RoHS Directive 2011/65/EU Annex II recast. The aqueous phase pH is stabilized at 4.8–5.2 through a phosphate-free buffer system, avoiding the amine synergists that often react with residual aldehyde species to form Schiff-base chromophores. Shelf life at 5–30 °C in sealed, nitrogen-blanketed IBC containers extends to 18 months, with redispersibility maintained after three freeze-thaw cycles conducted per ASTM D7149-05.

    Structural-Adhesive Bonding on Unprimed Polyolefin and Engineering Thermoplastics

    Prediction of lap-shear strength for low-VOC VAE dispersions on low-surface-energy substrates requires consideration of interfacial acid-base interactions rather than mechanical interlock alone. EcoVAE 1620 contains 1.2 mol% copolymerized acrylic acid, elevating the wetting envelope to a calculated surface tension of 42 mN/m at 10 ms bubble lifetime in maximum-bubble-pressure tensiometry. On corona-treated polypropylene film (surface energy 38 mN/m post-treatment), an application weight of 18 g/m² dry generates a 180° peel adhesion of 4.6 N/25 mm at a jaw separation rate of 300 mm/min (ASTM D3330/D3330M-04 Method A). Cohesive failure within the emulsion layer remains below 5 % of the fracture surface when the adhesive is compounded with 0.3 wt% of a diglycidyl ether crosslinker. Compatibility testing across a panel of seven commercial tackifier dispersions—rosin ester, terpene-phenolic, and C5/C9 hydrocarbon types—shows no macroscopic grit formation at tackifier loading up to 25 wt% on solids when the blend is agitated under vacuum at −0.09 MPa for 30 min in a planetary mixer.

    In edge-band adhesion trials on medium-density fiberboard (MDF) with 0.4 mm ABS edging, a hot-press cycle of 120 °C platen temperature and 0.6 MPa pressure for 45 s develops a heat-resistance limit of 92 °C (WATT 91 test, 500 g dead weight). Delamination between the emulsion layer and the ABS backer is the primary failure channel at temperatures above 95 °C, suggesting that surface activation of the thermoplastic edge via atmospheric plasma (50 W·min/m² dosage) is necessary when service conditions exceed 90 °C continuously.

    Lamination of open-cell melamine foam (density 9 kg/m³) to nonwoven PET carrier webs benefits from the controlled flow behavior of EcoVAE 1620. Application via engraved gravure cylinder (40 lines/cm, cell volume 28 cm³/m²) deposits a pattern that wets the foam struts without capillary-driven migration into the pore volume, a deficit that causes stiffening in grades formulated with excess low-molecular-weight coalescents. Air permeability of the bonded composite measured under ASTM D737-18 at a pressure differential of 100 Pa declines by less than 12 % relative to the uncoated foam, attributable to the absence of film-forming aids boiling below 250 °C.

    Comparison With Conventional Phthalate-Plasticized and Oxo-Biodegradable Vinyl Acetate Homopolymer Dispersions

    Two classes of historical emulsion products inform the differentiation parameters for EcoVAE 1620. Table 1 summarizes the key translation of laboratory-characterized properties to processing-relevant metrics.

    Table 1. Processing and performance indices relative to a representative phthalate-plasticized PVAc homopolymer and a silane-crosslinking hybrid dispersion.
    ParameterTest StandardEcoVAE 1620Plasticized PVAc HomopolymerSilane-Crosslinking VAE Hybrid
    VOC content (wt%)ASTM D6886-18< 0.052.8–4.2 (dibutyl phthalate-dependent)0.3–0.7 (methanol from hydrolysis)
    Dry-film elongation (%)ISO 37:2017 Type 2840 (no plasticizer)650 (at 10 phr DBP)210 (post-cure)
    Wet bond retention on beech (%)EN 204:2016 D3 cycle824578
    Oven-aging yellowness index (ΔYI)ASTM E313-20, 120 °C, 168 h3.49.72.1
    Machine-direction blocking onset (°C)Hot-block, 5 psi, 1 h624868

    The pronounced elongation of EcoVAE 1620 without external plasticizer eliminates the progressive embrittlement observed in dibutyl-phthalate-blended homopolymers after thermal aging exceeding 500 h at 80 °C. Phthalate migration to the adhesive-substrate interface, measurable via surface FTIR-ATR carbonyl peak growth at 1720 cm⁻¹ within 72 h of contact with rigid PVC, is entirely absent. Meanwhile, silane-crosslinking hybrid dispersions provide superior solvent resistance and elevated-temperature creep resistance but impose a narrow processing window limited by premature condensation of silanol groups at pH > 6.5. EcoVAE 1620 requires no pH adjustment before compounding and can be processed on standard atmospheric-pressure laminators without controlled-humidity enclosures, a logistical constraint that restricts silane-functional grades to plants with dew-point control below −5 °C.

    In cold-chain label converting, where adhesive debonding at −20 °C must remain below 5 % of the label face, the biphasic morphology of EcoVAE 1620 sustains peel values of 3.8 N/25 mm on high-density polyethylene bottles stored at −25 °C for 72 h, compared with 0.9 N/25 mm for a DBP-plasticized PVAc control and 1.4 N/25 mm for a competing low-VOC VAE grade carrying 10 wt% ethylene in a unimodal distribution. The gap widens when labels are subjected to condensation cycling: 50 transitions between −30 °C and +20 °C at 95 % RH produce no tunneling or edge lift in the EcoVAE 1620 samples, while the unimodal low-VOC grade exhibits 17 % edge lift after 12 cycles.

    Regulatory and Hygienic-Article Suitability Under Current Food-Contact Frameworks

    Migration testing under EU Regulation 10/2011 simulant D1 (ethanol 50 % v/v, 40 °C, 10 days) on a 10 µm dry film yields total non-volatile residue below the 10 mg/dm² overall migration limit. Specific migration of ethylene glycol and diethylene glycol, analyzed by LC-MS/MS with a quantification limit of 0.01 mg/kg, returns values below the detection threshold. The absence of alkylphenol ethoxylate surfactants—confirmed by negative-mode ESI-MS scan—aligns with the REACH Annex XVII restriction on nonylphenol compounds. For indirect food-contact adhesives used in paper and board packaging, compliance with BfR Recommendation XXXVI and FDA 21 CFR 175.105 is supported by the formulation’s exclusion of biocides and formaldehyde donors. The low equilibrium moisture uptake (2.1 % after 24 h immersion at 23 °C, ISO 62:2008) reduces the risk of microbiological growth in glue trays left stagnant over weekend shutdowns, a common contamination pathway in high-humidity packaging halls.

    Medical nonwoven disposables—surgical drape lamination and face-mask ear-loop anchoring—represent an emerging area where the low-odor profile of EcoVAE 1620, quantified as < 0.5 on the VDA 270 C3 odor scale after 24 h of ventilation, meets the sensory requirements of cleanroom environments. Cytotoxicity testing per ISO 10993-5:2009 on L-929 fibroblast cells shows no reduction in cell viability at 100 % extract concentration, consistent with the non-cytotoxic classification.

    Published data for the high-frequency dielectric welding of EcoVAE 1620 films in medical fluid-bag applications is limited. Early trials on 0.3 mm cast films using a 27.12 MHz generator with a 5 kW output and a 3 s seal cycle indicate a burst pressure exceeding 35 kPa when the film is pre-conditioned to 6 % moisture content; below 2 % moisture, cohesive seal failure occurs at the weld periphery. Operators should therefore control ambient humidity to 40–55 % RH during converting until further optimization of the dielectric formulation is completed.

    Where Long Open-Time and Rapid Set Conflict in Assembly Operations

    The open-time/set-speed conflict in waterborne laminating adhesives often forces a choice between machine-speed reduction or additional drying capacity. EcoVAE 1620 extends open time to 85–110 s on 80 g/m² kraft linerboard at 23 °C and 50 % RH (internal method, wet-film thickness 50 µm), while its set speed—defined as the time to achieve 0.3 N/mm² fiber-tear resistance—clocks at 12 s under identical conditions when a 0.15 s infrared flash (2.8 µm peak wavelength) precedes nipping. This divergence arises from a two-stage water-release mechanism: rapid evaporation of interstitial water from the bimodal packing geometry, followed by a slower diffusion-limited release from the high-ethylene domains. In a commercial assembly line running 80 m/min with roll-nip pressure of 3.5 N/mm, the bond strength at 0.5 s post-nip surpasses 0.25 N/mm², sufficient to prevent spring-back in fold-over carton side seams without compression-section extension.

    Coating-pan operations for fiber-reinforced composite preforms present a harder test because the dwell time between impregnation and lay-up varies unpredictably. A 30-min open-time tolerance is demanded. EcoVAE 1620 applied at 22 % solids onto 300 g/m² glass-fiber mat retains tack measurable as a 0.9 N probe-tack force (ASTM D2979-16, probe diameter 5 mm) after 35 min in a 27 °C/35 % RH lay-up room. Incorporation of 1.5 wt% of a rosin-based dispersion solids extends the tack retention to 52 min without shifting the MFFT above +2 °C. Operators must, however, maintain diurnal temperature fluctuation within ±3 °C; a morning shift start at 18 °C can depress tack by 40 % until the adhesive reaches thermal equilibrium.

    Processing Equipment Corrosion and Cleaning Regimes

    Wetted components in contact with EcoVAE 1620 require 316L stainless steel or higher-grade passivated alloys if the fluid remains stagnant for periods exceeding 8 h. The low pH buffer, while necessary for stability, generates a weak cathodic reaction on unprotected 304 steel, observed as pitting corrosion after 2000 h of intermittent duty in a pilot-scale nozzle applicator. Cleaning protocols utilize a two-stage sequence: a 40 °C water flush at 2 bar pressure to displace the bulk dispersion, followed by a 0.5 % sodium carbonate solution circulated for 15 min at 1 m/s linear velocity. Alkaline cleaning temperatures must not exceed 50 °C to avoid saponification of residual acetate groups, which produces a viscous carboxylate gel that clogs filter screens downstream. A final rinse with deionized water until conductivity of the effluent drops below 20 µS/cm ensures complete removal of cleaning agents.

    Drying-oven hygiene benefits from the absence of semi-volatile coalescents that condense on heat-exchanger fins. Gravimetric measurement of condensate on aluminum panels suspended in the exhaust stream of a 3-zone convection dryer operating at 130 °C inlet temperature registers 0.02 mg/cm² after 72 h continuous operation, compared with 1.8 mg/cm² for a typical coalescent-dependent VAE. This low fouling rate extends intervals between oven cleanouts and reduces the fire load in the extraction ductwork, directly addressing a root cause of insurance-related downtime in coating plants.