Products

Products

Anhui Liwei Chemical Co., Limited.

VINAVIL EVA 202 VAE Emulsion

    • Product Name: VINAVIL EVA 202 VAE Emulsion
    • Factroy Site: Lingwu, Yinchuan, Ningxia, China
    • Price Inquiry: sales2@liwei-chem.com
    • Manufacturer: Anhui Liwei Chemical Co., Limited.
    • CONTACT NOW
    Specifications
    HS Code 554230
    Product Name VINAVIL EVA 202
    Chemical Family Vinyl Acetate-Ethylene (VAE) copolymer emulsion
    Appearance Milky white aqueous dispersion
    Solids Content 55 ± 1 %
    Viscosity 2000 - 4000 mPa·s at 25°C
    Ph 4.5 - 5.5
    Density 1.04 - 1.06 g/cm³ at 20°C
    Average Particle Size 1 μm
    Glass Transition Temperature -5 °C
    Minimum Film Forming Temperature 0 °C
    Residual Monomer < 0.1 %
    Film Appearance Clear, flexible, water-resistant film

    As an accredited VINAVIL EVA 202 VAE Emulsion factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Supplied in 200 kg drums or 1,000 kg IBC totes, with sealed liners and hazard labeling for safe storage.
    Container Loading (20′ FCL) 20′ FCL: VINAVIL EVA 202 VAE Emulsion loaded in IBCs/drums, secured and braced, full container utilization, no co-loading.
    Shipping VINAVIL EVA 202 is a vinyl acetate-ethylene (VAE) copolymer emulsion supplied in drums, IBCs, or bulk tankers. It is non-hazardous for transport, but should be kept above freezing and protected from extreme heat. Ship via standard freight with secure containment, avoiding prolonged storage below 5°C.
    Storage Store VINAVIL EVA 202 VAE Emulsion in its original, tightly sealed containers in a cool, dry, well-ventilated area, ideally between 5°C and 35°C. Protect from freezing, direct sunlight, and excessive heat. Avoid exposure to air and contamination. With proper storage, the product typically remains stable for up to six months.
    Shelf Life Shelf life is 12 months from manufacture when stored unopened at 5–35°C, protected from frost and direct sunlight.
    Application of VINAVIL EVA 202 VAE Emulsion

    In converting lines where clay-coated SBS board is bonded to corrugated medium at speeds between 80 m/min and 150 m/min, VINAVIL EVA 202 is compounded as the main film-forming polymer in waterborne laminating adhesives. The dispersion is blended with a rosin ester tackifier dispersion at 15–25 dry wt% of total binder, a triethyl citrate or dipropylene glycol dibenzoate plasticizer at 5–12 wt% of wet adhesive, and a defoamer/levelling package at 0.1–0.5 wt%. The final adhesive is typically held at 2,000–3,500 mPa·s Brookfield RVT at 25°C for roller coater stability. Wet add-on is controlled between 20 g/m² and 40 g/m² on a 600 mm wide roll coater, followed by nip lamination at 2–5 bar and infrared tunnel drying at 90–120°C for 8–15 s. The finished converting product is a folding-carton or set-up box board with a fibre-tearing bond when delaminated dry. Compliance for food-contact adhesives is assessed under FDA 21 CFR 175.105 for indirect adhesives and, where relevant, EU Regulation 10/2011 with an overall migration limit of 10 mg/dm² for the finished food-contact article. Batch-to-batch viscosity drift in the laminating bath is a known production failure mode. Adding more than 2–3% water in a single shot drops wet tack faster than reformulation with a polyurethane associative thickener. Process operators must avoid pH adjustment above 8.5 because the anionic stabilisation of the VAE dispersion begins to collapse.

    What Limits High-Speed Card Web Saturation with an Anionic VAE Binder?

    The nonwoven binder bath is not a static reservoir; it is a recirculating system in which shear stability, foam generation, and anionic charge balance control whether a carded web can leave the dryer without pinholes and with reproducible tensile strength. In a saturation bonding line running viscose/polyester or polypropylene staple webs at 50–200 m/min, the bath is maintained at 8–20% total solids. Wetting is adjusted with a sulfosuccinate or alcohol ethoxylate surfactant at 0.1–0.4 wt% of bath, and a silicone-free defoamer is dosed at 0.05–0.15 wt% to control foam generated by the padder nip. The web is passed through a two-roll or three-roll padding mangle with nip pressures of 2–4 bar to achieve wet pick-up between 70% and 150%. Drying is carried out in a multi-zone belt oven with zone set points of 110°C, 135°C, and 155°C. The final residual moisture target is 1–3% because overdrying above 170°C produces measurable yellowing and embrittlement. For wipe and hygiene-grade fabrics requiring wet strength, 1–3 phr of ammonium zirconium carbonate or a blocked polyisocyanate dispersion is added before the bath enters the mangle. The pH is kept below 8.2 to prevent premature gelation in the circulation loop. Tensile and wet tensile are evaluated according to ISO 9073-3 and NWSP 110.4. The finished nonwoven is used for technical wipes, acquisition layers, tablecover laminates, and automotive interior substrates. The primary incompatibility is with cationic wet-end additives and with high-hardness process water above 300 ppm CaCO₃ equivalent, which can reduce binder drainage uniformity and create streaky add-on across the web width.

    When Carpet Precoat Formulations Move from SBR to VAE Emulsion

    A replacement of carboxylated styrene-butadiene latex in a precoat compound is not a drop-in substitution because VAE exhibits different shear viscosity, filler acceptance, and drying coalescence behaviour. In carpet and automotive mat backcoating, VINAVIL EVA 202 is compounded at 100 parts dry polymer with 200–400 phr calcium carbonate, 1–3 phr polyacrylate thickener, 0.5–2 phr ammonium stearate froth stabilizer, and a biocide package. The compound is diluted to 75–85% total solids, applied on a puddle coater with a doctor blade gap of 0.5–1.5 mm, and optionally frothed with controlled air to a cup-weight reduction of 10–25%. Drying in a forced-air oven uses a ramp profile from 110°C to 160°C over 3–6 min. The initial zone must remain below the bubble point to avoid pinholes. Tuft bind is evaluated under ASTM D1335 and secondary backing peel under ASTM D3936. The finished goods are broadloom carpet, residential carpet tile, and automotive mat backing. The operational boundary is wet strength. Uncrosslinked VAE precoats show lower hot-wet strength than carboxylated SBR, so they are not specified for exterior or marine carpet unless an external crosslinker is used. High filler loadings above 400 phr can shift the rheology from shear-thinning to dilatant on the coater, producing streaks that are visible only after tufting.

    In dry-mix and two-component construction mortars, VINAVIL EVA 202 is handled as a liquid polymer modifier rather than a redispersible powder, which changes the plant sequence for installations that add liquid polymers at the mixer. The emulsion is added at 10–35 kg per 100 kg cement, equivalent to a polymer solids-to-cement ratio of about 0.05–0.20, depending on the target class and substrate. The mixing sequence is critical. Tempered water and emulsion are combined first with the cementitious powder in a high-shear paddle mixer at 300–500 rpm, then allowed to slake for 2–5 min before retempering. Pot life under 20°C and 50% RH is typically 40–90 min, but the emulsion must be protected from freezing and from direct contact with polyvalent metal salts that can cause coagulation. Modified tile adhesives are tested according to EN 12004 for classification, with additional liquid-applied membrane verification under EN 14891 where used as a two-component waterproofing slurry. The emulsion contributes flexibility and adhesion to low-porosity tiles. Published data for this specific VAE grade in any single EN 12004 classification is limited, and each plant formulation must be run through the full test matrix because cement alkalinity at pH above 12 can destabilize unmodified anionic dispersions. The terminal products are two-component tile adhesives, flexible grouts, patching mortars, and waterproofing slurries applied by trowel or roller.

    Process boundary data reported from converting and dry-mix lines
    Line configurationObserved failureControl measureBoundary condition
    Roll coater for laminatingViscosity drift from evaporative water lossAdd 2–3% water incrementallypH must remain below 8.5
    Padding mangle for nonwovenFoam entrapment at high web speedDefoamer at 0.05–0.15%Water hardness above 300 ppm CaCO₃ equivalent
    Puddle coater for carpetStreaking after filler loading exceeds 400 phrDoctor gap limited to 1.5 mmInitial oven zone below 120°C
    Mortar mixerShock destabilization from neat emulsion into cementDilute emulsion with tempered water firstMix temperature above 35°C shortens pot life

    Creep Resistance Is the Limiting Parameter in Cold-Press Wood Lamination

    Cold-press lamination imposes a different failure mode from hot-press lamination because the bond lacks the thermal relaxation that reduces internal stress in the adhesive line. VINAVIL EVA 202 is formulated for flat lamination of paper-backed veneer, polyvinyl chloride edgebanding, and high-pressure laminate to MDF or particleboard by blending it with a 10–25 wt% solution of partially hydrolysed polyvinyl alcohol at a dry weight ratio of 70:30 to 85:15, plus calcium carbonate filler at 5–12 phr and a preservative at 0.1–0.3 phr. The adhesive is roll-coated at 80–150 g/m² on the board face, assembled open for 5–15 min, and then cold-pressed at 0.5–1.2 N/mm² for 30–60 min. For hot-press operations, the same formulation is pressed at 90–120°C for 5–12 min. Dry and wet resistance are assessed under EN 204 and EN 205. D2 or D3 water resistance classes require wet tensile testing after 4 days of cold-water immersion, and D3 formulations typically need an added isocyanate or glyoxal-based crosslinker. The primary limitation is creep under sustained load at temperatures above 50°C. The product is not specified for load-bearing wood structures tested under EN 301 or for laminates subjected to prolonged direct heat sources. Terminal finished goods include furniture panels, kitchen cabinet doors, and interior door skins.

    Compliance and performance anchors for VINAVIL EVA 202 in five downstream sectors
    ApplicationPerformance testRegulatory anchorTypical formulation window
    Packaging laminating adhesiveASTM D1876 T-peelFDA 21 CFR 175.105, EU 10/20115–12 wt% plasticized wet adhesive base
    Nonwoven binderISO 9073-3, NWSP 110.4REACH obligations8–20% bath solids
    Carpet precoatASTM D1335, ASTM D3936REACH, indoor VOC criteria100 dry phr base binder
    Cementitious tile adhesiveEN 12004, EN 14891EU Construction Products Regulation5–20% polymer solids on cement
    Wood laminationEN 204, EN 205EU harmonised health requirements70:30–85:15 VAE:PVOH dry blend

    Where interior low-VOC wall paint reformulation fails with high-Tg acrylic binders, VAE dispersions such as VINAVIL EVA 202 provide film formation at low coalescent demand because the polymer minimum film formation temperature is near 0°C. In a standard interior matt formulation, the pigment paste is dispersed on a high-speed disperser with a sawtooth blade at 20–30 m/s tip speed using 10–18 wt% titanium dioxide, 8–15 wt% calcined kaolin, 5–12 wt% talc, a polyacrylate dispersant at 0.3–0.8 wt%, and a defoamer. The let-down contains VAE solids at 20–35% of total binder solids, with coalescent at 0–2 wt% on binder and a synthetic thickener to reach a Stormer viscosity of 95–110 KU. The pH is raised slowly to 8.0–8.5 with dilute ammonia. Shock addition above pH 9 can produce micro-flocculation in the anionic dispersion. Volatile organic compound content is measured by ISO 11890-2 and benchmarked against the EU Directive 2004/42/EC limit of 30 g/L for ready-to-use interior matt wall and ceiling paints. The operational boundary is water resistance. VAE films are not suitable for exterior topcoats or continuous immersion service, and high pigment volume concentration formulations above 70% PVC require wet abrasion verification under ISO 11998 to avoid early burnishing and scrub failure. The finished product is an interior wall paint, primer, or ceiling paint with a flat to low-sheen finish.

    Paper Priming and Size-Press Binding for Inkjet Receptivity

    Surface-strength shortfalls on lightweight coated grades are addressed in the size press by blending oxidized starch with VAE emulsion to increase pick resistance without closing the sheet to ink absorption. A typical size-press formulation contains 70–90 dry parts oxidized starch and 10–30 dry parts VINAVIL EVA 202, plus calcium stearate at 0.5–1 part and a defoamer. The bath solids are maintained at 10–18%. The metering size press is run at 300–1,200 m/min with a dry pick-up target of 2–5 g/m², followed by cylinder or air-turn drying from 80–130°C. The VAE increases IGT surface strength measured under ISO 3783 and reduces dusting on subsequent printing and converting lines. For food-contact board, the coated substrate is assessed for extractives under FDA 21 CFR 176.170 and FDA 21 CFR 176.180 for aqueous and fatty food types, while the wet-end and coating materials remain subject to REACH registration obligations. The finished reel is used as inkjet paper base, decorated board for packaging, or label face stock. The main limitation is barrier function. This surface treatment does not provide oil and grease resistance, so a separate fluorochemical-free topcoat or extrusion layer is needed for high-fat or high-moisture contents.

    Free Quote

    Competitive VINAVIL EVA 202 VAE Emulsion prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please contact us at +8615380400285 or mail to sales2@liwei-chem.com.

    We will respond to you as soon as possible.

    Tel: +8615380400285

    Email: sales2@liwei-chem.com

    Inquiry

    Get Free Quote of Anhui Liwei Chemical Co., Limited.

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    Supplied as an anionic/nonionic-stabilized aqueous dispersion of vinyl acetate-ethylene copolymer, VINAVIL EVA 202 VAE Emulsion is used in waterborne adhesive systems that require low-temperature film formation without external coalescing solvents. The ethylene comonomer disrupts poly(vinyl acetate) crystallinity and functions as an internal plasticizer, reducing the minimum film-forming temperature and limiting the need for dibutyl phthalate or diisononyl phthalate. In laminating operations, the product is typically applied by roller coater or slot-die coater to corona-treated polyester film, coated paper, or paperboard; wet coat weights of 18–25 g/m² are common for paper-to-film laminates, although line speed must be adjusted when high humidity increases the dryer load. The dispersion is shear-thinning and must be protected from prolonged high-shear pumping because air entrainment and temperature rise above 40 °C can reduce colloidal stability.

    Food-contact suitability requires verification against the specific substrate and laminate construction under Commission Regulation (EU) No 10/2011 and German BfR Recommendation XIV; lot-specific manufacturer declarations should be requested. The dispersion is supplied as an APEO-free and plasticizer-free grade, but the formulated adhesive may require additional volatile organic compound testing according to ISO 11890-2.

    Dispersion composition and specification envelope

    Representative property ranges for the as-supplied dispersion are listed in Table 1. Samples are conditioned at 23 °C and 50 % RH according to ISO 291 unless the method specifies otherwise. The values are typical ranges rather than specification maxima or minima; release criteria should be drawn from the manufacturer’s certificate of analysis.

    Typical property envelope for VINAVIL EVA 202 VAE Emulsion
    ParameterMethodReported range
    Solids contentISO 325154–56 %
    pHISO 9764.0–5.5
    Brookfield RVT viscosity at 20 min⁻¹, 25 °CISO 25553000–5000 mPa·s
    DensityISO 28111.06–1.08 g/cm³
    Minimum film-forming temperatureISO 2115≤0 °C
    Glass transition temperature of dried filmISO 11357-2-15 °C to -10 °C
    Average particle sizeISO 133200.8–1.5 µm
    Residual vinyl acetate monomerHeadspace GC≤1000 mg/kg

    The dried polymer has a glass transition temperature in the range of -15 °C to -10 °C as measured by differential scanning calorimetry according to ISO 11357-2. The low glass transition and sub-zero minimum film-forming temperature allow formulation without tributyl citrate or phthalate coalescents. The average particle size measured by laser diffraction per ISO 13320 lies in the sub-micrometre-to-low-micrometre range and contributes to mechanical stability under pumping and roller-coater shear. In production practice, gravure transfer becomes irregular when Brookfield viscosity exceeds approximately 1500 mPa·s at 20 min⁻¹; adjustment with deionized water is therefore common before long runs.

    Unlike many poly(vinyl acetate) homopolymers, VINAVIL EVA 202 does not require a coalescing solvent to form a continuous film at 5–10 °C. This difference is relevant in cold warehouse laminating operations where solvent contact is prohibited by workplace exposure limits. The product displays pseudoplastic behaviour; viscosity drops under roller-coater shear and recovers quickly enough to reduce strike-through on porous paper. Anti-foam selection is critical because mineral-oil defoamers can destabilize the dispersion, while silicone-based defoamers at 0.05–0.2 wt% are normally better tolerated.

    What formulation boundaries are imposed by colloidal stability?

    Because the dispersion is anionically stabilized and has an acidic pH, addition of ammonia or amines raises the system pH and may produce thickening or microflocculation. Long-term storage above pH 8 is not recommended because alkaline conditions accelerate hydrolysis of vinyl acetate units. Multivalent cations such as calcium from hard water reduce electrostatic repulsion; dilution water with hardness greater than 25 °dH should be softened before letdown. Freeze-thaw cycling can generate coagulum, so storage should remain between 5 °C and 35 °C. In a bulk storage tank, slow-speed anchor agitation at 30–60 min⁻¹ prevents sedimentation without introducing excessive air.

    For plasticized PVC flooring adhesives, the ethylene fraction provides resistance to plasticizer migration at the adhesive interface. Peel adhesion is evaluated under EN 1372 or EN 14259 depending on regional specification; because substrate formulation affects plasticizer type and concentration, published data for this specific product-substrate configuration is limited. Formulations with calcium carbonate filler loadings above 20 wt% require higher-shear dispersion and may need wetting agent adjustment to prevent separation during storage. When relative humidity exceeds 60 % RH, drying of paper-based laminates requires longer oven residence time or forced convection at 85–95 °C; otherwise residual moisture can reduce bond strength.

    When replacement of PVAc homopolymer or acrylic dispersion is evaluated

    In comparison with a poly(vinyl acetate) homopolymer of similar solids, VINAVIL EVA 202 shows lower film-forming temperature and improved adhesion to non-polar films. The PVAc homopolymer normally exhibits a minimum film-forming temperature near 15–20 °C and requires coalescent addition in winter; VINAVIL EVA 202 has a minimum film-forming temperature at or below 0 °C. Against acrylic dispersions, the VAE chemistry can provide higher wet tack on paper and lower raw material cost per dry kilogram, although the acrylic binder generally has superior ultraviolet stability and water resistance in exterior applications.

    Replacement on manufacturing lines requires rheology adjustment. Acrylic dispersions often possess pseudoplastic profiles with greater shear stability under high-speed pumping, whereas VAE can shear-thicken when air is entrained. Fouling on gravure cylinders can be reduced by maintaining pH between 4 and 5; below 3.5, the dispersion may thicken, and above 8, ammonia release and hydrolysis become operational concerns. Batch-to-batch viscosity variation is typically controlled within ±500 mPa·s when measured at 20 min⁻¹ and 25 °C, which is sufficient for most continuous gravure lines but may require in-line viscosity correction for narrow slot-die coaters.

    Assessing performance differences among waterborne dispersion families

    The principal difference between VINAVIL EVA 202 and standard PVAc homopolymer dispersions lies in the ethylene comonomer content. Ethylene lowers the glass transition temperature and reduces the hydrophilic character of the copolymer, improving wetting of low-energy surfaces such as polypropylene and polyethylene after corona treatment. The comonomer also disrupts regular chain packing, which limits cohesive strength at elevated temperature; therefore the product is not used where sustained service temperatures exceed approximately 60 °C without crosslinker modification. Heat resistance is measured by shear adhesion failure temperature according to DIN EN 14257 or equivalent internal methods; published data for this specific configuration is limited and must be generated for each formulation.

    Compared with a low-ethylene VAE grade, VINAVIL EVA 202 occupies a mid-ethylene position for balance between film flexibility and heat resistance. Lower ethylene grades provide higher shear adhesion but require coalescent addition, while higher ethylene grades provide lower glass transition and longer open time but may exhibit blocking at lower stacking temperatures. In paper-to-paper laminating, the open time is typically extended by adding poly(vinyl alcohol) solution at 5–15 wt%; the poly(vinyl alcohol) increases machine-speed wet tack but can shorten shelf life if the final pH drops below 3.5. The product is pumped with progressive cavity or diaphragm pumps rather than centrifugal pumps to reduce foam generation in recirculating coating pans.

    For wood assembly or furniture lamination, the dispersion may be evaluated according to EN 204 for non-structural wood adhesives or EN 205 for shear strength, but the primary commercial application remains paper, packaging, and PVC flooring lamination. The dispersion is not recommended for continuous immersion service because the vinyl acetate repeat units are hydrolytically sensitive under prolonged wet alkaline conditions. When the target substrate is plasticized PVC, the ethylene comonomer reduces plasticizer migration into the adhesive interface, but the formulated adhesive must still pass the relevant flooring adhesive endurance test under EN 14259. The selection of wetting agent and defoamer is formulation-specific; silicone-based defoamers at 0.05–0.2 wt% and acetylene-diol wetting agents at 0.1–0.3 wt% are common starting points, but compatibility should be confirmed by oven-aging the formulated dispersion for 14 days at 40 °C before production-scale trial.